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  • Polymer and Materials Science  (167)
  • unknown  (11)
  • 42.75
  • 1950-1954  (178)
  • 1945-1949
  • 1952  (178)
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  • 1950-1954  (178)
  • 1945-1949
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  • 1
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polyvinyl alcohol was condensed with straight and branched chain aldehydes (CnH2nO, n = 2 to 8) to varying degrees of completion. Measurements on resins and plasticized compositions included apparent modulus of elasticity at various temperatures, brittle temperature, tensile strength and elongation, and solubility. From these measurements it is concluded that: (1) Increasing degree of acetalization results in lowered transition temperature, lower stiffness at transition, narrower transition range, higher brittle temperature, decreased tensile strength, and shift in solubility toward solvents of lower dielectric constant. (2) Acetals of higher normal aldehydes have lower transition and brittle temperatures, lower tensile strength, and more limited solubility. (3) Branched chain aldehydes have higher transition and brittle temperatures than their normal isomers.
    Zusätzliches Material: 17 Ill.
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  • 2
  • 3
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 321-335 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Vulcanization with sulfur is ascribed to the formation of sulfur radicals which are believed to copolymerize with the rubber molecule double bonds. Hydrogen sulfide is proposed as necessary for chain initiation but when formed in sufficient amounts serves as a chain terminator. This is believed to lead to numerous self-limiting features including ceiling temperatures, post-vulcanization and delayed action effects. Initiation may result from the oxidation of H2S to sulfur radicals and termination to the formation of HS radicals.
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  • 4
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 346-349 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Tab.
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  • 5
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The high crystallite melting point of polyethylene terephthalate (Terylene) compared with the melting points of the aliphatic polyesters emphasizes the significance of the p-phenylene linkage as an important factor determining polymer properties. A consideration of other polymer structures containing the p-phenylene linkage shows that its influence is independent of any polar groups which may be present. X-ray examination of the crystallite structure of polyethylene terephthalate and related substances has revealed no evidence of strong intermolecular forces.From a study of co-polyesters based upon polyethylene terephthalate with aliphatic dibasic acids it is shown that the melting point of compositions containing more than 40 mole per cent of ethylene terephthalate is essentially independent of the aliphatic di-basic acid employed. The Flory relationship between crystallite melting point and mole fraction of the units forming the crystallites shows fair agreement with the results obtained. The calculated latent heat of fusion of polyethylene terephthalate approaches closely to that of the corresponding aliphatic polyesters, and suggests that the high melting point induced by the p-phenylene linkage is due to chain rigidity rather than to strong interchain attraction.This rigidity is consistent with the second order transition temperatures of such polyesters. It is shown that second order transition temperature is a linear function of the number of p-phenylene linkages per unit chain length. The p-phenylene linkage reduces the possibilities of change of shape available to a given length of chain, so accounting for the low entropy of crystallization and high melting point of polyethylene terephthalate.Evidence is advanced for the isomorphism of adipyl and terephthalyl linkages in linear polyamides. The absence of isomorphism in polyethylene adipate/terephthalate copolymers is ascribed to the weakness of the interchain forces.
    Zusätzliches Material: 12 Ill.
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  • 6
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A sample of copolymer of divinylbenzene and styrene has been prepared and fractionated. Using the techniques of light scattering and viscometry the relations between the molecular size, intrinsic viscosity, and weight-average molecular weight have been determined. The results may be interpreted in terms of the already existing theory of branched polymers. The curve of logarithm of intrinsic viscosity plotted against logarithm of molecular weight shows clearly the effect of branching in the polymer chains, the intrinsic viscosities of the higher molecular weight fractions being low compared to those of pure polystyrene. The mean square radius of the molecules as determined by light scattering shows similar effects, though complications obscure the picture. Some of the other solution properties of the branched materials also are peculiar. The results show that the semiquantitative determination of branching is possible in this way.
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  • 7
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Branching and cross-linking are noted in emulsion and mass polymerizations involving vinyl benzoate and nuclearly substituted vinyl benzoates. A theory is proposed to account for this phenomenon based on free radical addition to the benzoate nucleus. Six new vinyl esters of substituted benzoic acids are described.
    Zusätzliches Material: 3 Tab.
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  • 8
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: This paper presents certain results concerning the solubility of polyvinyl chloride in mixed solvents of which one is carbon disulfide or acetone. The technique consists in immersing a pressed disc of the polymer in the mixed solvent at constant temperature for a fixed length of time and observing the depth of penetration of the solvent into the sectioned disc. Three classes of solvents are distinguished. (1) Inert solvents producing no change. (2) “Disintegrating liquids” in which dissolution proceeds without previous visible swelling. (3) Solvents producing swelling (“gelatinization”) and sometimes subsequent dissolution. The speed of penetration of several pairs of solvents are examined over the whole concentration range and a maximum in the depth of penetration is found on varying the solvent composition, at near stoichiometric proportions. It is suggested that the speed of penetration is closely related to solvent power, and the importance of solvation of the polymer (perhaps strong enough to be called “molecular combination”) both in swelling and in completed dispersion is stressed. It is concluded that class 3 solvents (high dipole moments) increase the solubility of class 2 solvents (low to zero dipole moment) by the solvation effect.
    Notizen: Après avoir rappelé quelques considérations générales concernant la mise en solution des hauts polymères dans les liquides organiques, les auteurs relatent les principaux résultats de leurs expériences sur la solubilisation des chlorures de polyvinyle industriels dans les liquides binaires. Ils montrent qu'en pastillant par compression le polymère il est possible d'examiner sur ces comprimés l'action de divers liquides et distinguent: (1) les liquides inertes; (2) les liquides désagrégeants; (3) les liquides gélatinisants. Les meilleurs solvants binaires se présentent généralement sous forme de mélange d'un liquide gélatinisant et d'un liquide désagrégeant ce qui revient à combiner l'action d'un liquide polaire et d'un liquide non polaire.Ils montrent ensuite comment on peut apprécier le pouvoir solvant d'un solvant binaire en fonction de sa composition en mesurant la vitesse de pénétration de ce dernier dans une pastille de polymère. Les courbes obtenues ainsi accusent des maxima correspondant sensiblement à des rapports stoechiométriques simples entre les molécules des deux constituants.Ils insistent ensuite sur la nécessité de considérer un phénomène de solvatation comme facteur de gélification et, par suite, comme premier stade de la dissolution. Ceci s'appuie sur leur détermination des degrés de solvatation du chlorure de polyvinyle au moyen de la méthode graphique des restes. Ces solvates font intervenir un seul ou deux des constituants du liquide binaire utilisé comme solvant. Mais dans le cas d'une fixation simultanée des deux constituants du solvant sur le polymère il y a lieu de considérer une action individuelle de ces deux constituants, les propriétés physiques des mélanges étudiés excluant en effet l'hypothèse de complexes d'addition dans le solvant binaire lui-même.Enfin les auteurs pensent que la solvatation des molécules du polymère persiste dans la solution colloïdale de ce dernier et annoncent qu'ils poursuivent actuellement leurs essais dans le but de mettre cette solvatation en évidence.
    Zusätzliches Material: 4 Ill.
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  • 9
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Thermokinetic aspects of adsorption and of the heat evolved as functions of the amount of substance absorbed per weight gram of adsorbent were followed by measurements on a microcalorimeter (especially designed for slow processes). For insoluble substances these experiments make possible evaluation of the area and surface of powders and of the approximate expansion rate of the films, as well as a study of the activated surface fraction. For soluble compounds they show the generally well-known phenomenon of adsorption which precedes dissolution and make possible the interpretation of the mechanism of dissolution. For macromolecular substances they permit classification of the solvents and gelatinizing agents according to their activity, and the study of swelling, the complex of solvation, etc.
    Notizen: L'étude thermocinètique de l'adsorption et celle de la chaleur dégagée en fonction de la masse du corps adsorbé par unité de masse de l'adsorbant réalisées au microcalorimètre (spécialement adapté à la mesure des phénomènes lents) nous parait présenter un grand intérêt: pour les corps insolubles ces études permettent l'évaluation des surfaces des poudres, la mesure approximative de la vitesse d'expansion des films, l'étude de la fraction activée des surfaces; pour les corps solubles elles permettent de mettre en évidence le phénomène très général de l'adsorption qui précède la dissolution et d'interpréter le mécanisme de la dissolution; pour les substances macromoléculaires elles permettent de classer les solvants ou gélatinisants suivant leur activité, d'étudier le gonflement, les complexes de solvatation, etc. Tout cela démontre le nécessité d'organiser des Centres bien équipés de microcalorométrie des phénomènes lents.
    Zusätzliches Material: 7 Ill.
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  • 10
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The synthesis and the properties of permutoids with ionic active groups and the kinetics of the decomposition of diazoacetic ester and of nitrosomethylurea through the ionic active groups are dealt with. A discussion follows of the synthesis of high polymers and permutoids with active groups of the chlorophyll and hemin series obtained by the introduction of the corresponding active groups into high-polymeric compounds, by copolymerization, and by inclusion of the prosthetic group in the polycondensation process. A report is added on the optical properties of the high-molecular compounds provided with active groups and on remarkable differences between low-molecular compounds in a dissolved state and as active groups linked to high polymers. The apparatuses developed for taking absorption and reflection spectra are described. Finally, the catalytic effect of the high polymers provided with active groups of the hemin series is examined.
    Zusätzliches Material: 11 Ill.
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  • 11
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 243-253 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A general discussion about the method of colloid titrations is given in this report. A new titration method is based on the stoichiometric combination of positive and negative colloid ions. The end point is decided by indicators (known as metachromatic coloring matters) like toluidine blue. The standard colloid reagents are P.V.S.-K (potassium salt of polyvinyl alcohol sulfate) and Macramin (N-polymethylated chitosan derivatives). The typical operations of this method are described briefly: the direct, indirect, and differential titration methods. The colloid titration curve is somewhat different from the acid-base titration curve obtained potentiometrically, but it is characteristic and reproducible under definite conditions and so it is useful in quantitative and qualitative analysis. This titration may be carried out even under extraordinary dilute conditions (5 × 10-4 N) and the entire process is quite similar to the usual acid-alkali titration. The precision is below ±ca. 5% if the method is carefully followed.
    Zusätzliches Material: 5 Ill.
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  • 12
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 255-256 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 13
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The study of the rate of polymerization per particle in emulsion systems has been extended to include the following monomers and initiator systems: TextMonomerInitiator SystemStyrenePersulfateStyreneCHP-TETAIsopreneDIBHP-TEPAIn all cases, linear rates of polymerization were obtained in the region where the number of particles can be considered as remaining constant (30-60% conversion). Furthermore, the addition of catalyst in this region did not affect the rate of polymerization, so that a rate per particle could be calculated. From the rates per particle, the following absolute propagation rates were calculated for styrene and isoprene, and are compared with values obtained for styrene from photoinitiation studies: TextMonomerCatalyst systemEact.Akp at 60°C.StyrenePersulfate7.44.1 × 107277StyreneCHP-TETA8.43.3 × 107221StyrenePhotoinitiation7.82.2 × 107176IsopreneDIBHP-TEPA9.81.2 × 10850
    Zusätzliches Material: 3 Ill.
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  • 14
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 337-343 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: An x-ray diffraction camera, especially adapted for the study of fibers and high polymers, has been designed. By using only pure monochromatic light, obtained by reflection on a crystal of curved quartz (method of Guinier), it is possible to have the sample in a well controlled atmosphere and at a given temperature. The film is separated from the “laboratory-space” and maintained in vacuo. By this technique it was possible to improve considerably the quality of the diagram received.
    Notizen: Une chambre de diffraction de rayons X spécialement adaptée à l'étude des fibres et des hauts polymères a été construite. Conçue de façon à utiliser un rayonnement strictement monochromatique obtenu par réflexion sur un cristal de quartz courbé (méthode Guinier), elle permet deplacer l'échantillon dans une atmosphère contrôlée et à une température déterminée. Le film est isolé de “l'espace laboratoire” et est maintenu dans le vide. La qualité des diagrammes a été considérablement améliorée par cette technique.
    Zusätzliches Material: 6 Ill.
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  • 15
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 289-311 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Graft vinyl copolymers have been prepared by chain transfer reaction between monomer radical and polymer molecule, followed by addition of monomer to the “macroradical.” For this purpose vinyl monomers have been polymerized in the presence of appreciable amounts (25% or more) of foreign polymer, with benzoyl peroxide as catalyst (0.5% on monomer). The separation of the graft copolymers from the other homopolymers present in the mixture is based on differences in the solubility of these products. Experiments are carried out with vinyl acetate with polymethyl methacrylate at different temperatures, 75°, 85°, and 95°C.; the graft percentage depends considerably on t°, and the following values, respectively, 15, 32, and 53% for vinyl acetate are obtained from chemical and infrared analysis. These graft copolymers were identified by their solubility properties and their osmotic and viscometric behavior, values of k′ (Huggins' constant) and μ varying greatly for a mixture of both polymers (a true copolymer and a graft copolymer) where the molecular weight and the per cent of vinyl acetate are the same. In the same way, it is possible to obtain a graft copolymer by polymerization of vinyl chloride in the presence of polymethyl methacrylate. It has not been found possible to carry out the inverse reactions, namely, the polymerization of methylmethacrylate onto polyvinyl acetate or polyvinyl chloride, owing to fractionation of the polymers. Similar experiments were carried out at different temperatures with styrene on polymethyl methacrylate and with methyl methacrylate on polystyrene. In both cases the reactions are successful, and are characterized by a strong increase in solubility of the polystyrene fraction. In the first case, the amount of solubilized polystyrene increases with increasing temperature. These graft copolymerizations are related to degradation measurements described elsewhere and to the stability of the radicals formed.
    Notizen: Des copolymères greffés ont été préparés par réaction de transfert de chaǐne entre un radical monomérique et une molécule de polymère suivie de l'addition de monomère au macroradical. Dans ce but, les monomères vinyliques ont été polymérisés en présence de quantités appréciables (25% et plus) de polymère étranger, en présence de peroxyde de benzoyle comme initiateur (0.5% par rapport au monomère). La séparation des copolymères greffés des autres homopolymères présents dans le mélange est basée sur les différences de solubilité de ces produits. Les expériences ont été menées au départ d'acétate de vinyle en présence de polyméthacrylate de méthyle à différentes températures, savoir 75°, 85° et 95°C.; le taux de greffage dépend fortement de la t°, et atteint respectivement 15, 32 et 53% d'acétate de vinyle (analyses chimiques et infra-rouges) Ces copolymères greffés ont été identifiés par leurs propriétés de solubilité et leur comportémént osmotique et viscosimétrique; les valeurs de k′ (constante de Huggins) et μ varient considérablement si on compare un mélange de polymères, un copolymère habituel et un copolymère greffé, dont les poids moléculaires et le taux d'acétate de vinyle sont semblables. De la měme façon, il a été possible d'obtenir un copolymère greffé par polymérisation du chlorure de vinyle en présence de polyméthacrylate de méthyle. Les réactions inverses toutefois, savoir la polymérisation du méthacrylate de méthyle en greffage sur les acétate ou chlorure de polyvinyle, n'ont pu ětre mises en évidence par des opérations de fractionnement. Des expériences semblables ont été effectuées à différentes températures avec le styrène en présence de polyméthacrylate de méthyle, et inversément le méthacrylate de méthyle en présence de polystyrène. Dans les deux cas les réactions réussissent et se manifestent par une solubilisation de la fraction polystyrénique. Dans le premier cas, la quantité de polystyrène solubilisé croǐt avec une augmentation de température. Ces copolymérisations par greffage sont reliées aux phénomènes de dégradation, décrites ailleurs, et à la stabilité des radicaux formés au cours des réactions.
    Zusätzliches Material: 22 Ill.
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  • 16
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 365-370 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The reaction of polymethacrylamide, [-CH2C(CH3)(CONH2)-]n, in aqueous solution with hypobromite and hypochlorite has been investigated. Different reaction procedures yielded polymers which were similar, and which contained a small number of primary amino groups, considerable carboxyl and unreacted amide groups and, probably, alkylacylurea groups formed by interaction between adjacent isocyanate and halogenoamide groups. Analytical data supporting these conclusions are presented. The polymer from the Hofmann reaction is soluble in dilute alkali and also in strongly acid media, precipitating on dilution. Methacrylamide monomer reacts with hypochlorite to give N-α-methylvinyl-N′-methacrylurea and acetone.
    Zusätzliches Material: 5 Ill.
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  • 17
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 409-423 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: When the acetate groups of polyvinyl acetate are removed and subsequently restored, the viscosity of the polymer is usually decreased. It is found that after such processing, vinyl acetate polymers prepared at a given temperature approach a maximum viscosity regardless of the viscosity of the original resins. This maximum is increased by lowering the temperature of polymerization and is different for other vinyl esters. The extent of degradation is negligible at low conversions. It is concluded that this phenomenon is characteristic of the monomer. The chemical bond responsible for the degradation has many of the properties of ester linkages. The resins degrade with both bases and acids although the latter catalyst sometimes requires the presence of water. They also degrade when heated in a solution of pyridine, acetic acid and acetic anhydride. The extent of degradation closely parallels the degree of hydrolysis. It is suggested that these ester linkages are formed during polymerization as a result of transfer with the carbon-hydrogen bonds of the acetate groups of both monomer and polymer. Evidence of another transfer reaction involving the vinyl group, but having no bearing on the degradation, is also advanced. If polyvinyl acetate is alcoholized with an acid catalyst, in the absence of water, the processed resin may have a higher viscosity than would be the case with an alkaline catalyst. How much higher is governed by the type of initiator used in the polymerization. This suggests that polymer molecules may be united under these conditions, but the nature of the reaction is obscure.
    Zusätzliches Material: 2 Ill.
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  • 18
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 445-445 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 19
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The dynamic properties of low molecular weight polyisobutylene and silicone oils have been investigated over a range of frequencies and temperatures. When subjected to oscillating stresses, these materials behave as though they had a shear modulus as well as a viscosity. Dynamic viscosities and rigidities have been determined at frequencies between 10 and 100 cycles per second and at temperatures between -50° and +60°C. Falling ball viscosities were also obtained over the same temperature range. In general, moduli increase with increasing frequency and decreasing temperature while dynamic viscosities decrease with increasing frequency and increasing temperature. At room temperature and above, the dynamic viscosity varies very little with the frequency and is essentially the same as the falling ball viscosity. At lower temperatures the dynamic viscosity decreases considerably with increasing frequency but extrapolates to the falling ball viscosity at zero frequency. If these materials are regarded as complex Maxwell liquids, the dynamic rigidities and viscosities may be written as functions of a “reduced frequency” equal to the frequency multiplied by an exponential of a constant divided by the absolute temperature. This constant can be evaluated from the slope of the linear plot of the logarithm of the falling ball viscosity over the absolute temperature versus the reciprocal of the absolute temperature. For a given material a single constant suffices to bring the data at all frequencies and temperatures into a single plot similar to that used by Ferry.
    Zusätzliches Material: 8 Ill.
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  • 20
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: When heated in a vaccum at 325° to 375°C., polystyrene yields mainly the monomer and some dimer, trimer, tetramer, etc., indicating that the breaks in the molecular chains occur largely at the ends. Polyethylene, under similar conditions, but at a some-what higher temperature, yields fragments of an average molecular weight of about 700, indicating that the molecular chains break, mostly at random positions. A study was made of rates of thermal degradation of these two polymers by measuring rates of loss of weight of samples by means of a very sensitive tungsten spring balance enclosed in a vaccum. The samples were limited to 5-6 mg. in order to avoid spattering during degradation. Rate curves plotted against per cent loss of weight by volatilization indicate that in the case of polystyrene the process is intermediate between a zero and first order reaction, while in the case of polyethylene, the process approximates a first order reaction. Activation energies were calculated on the basis of rates of degradation at various temperatures. The values thus obtained for polystyrene and polyethylene are 58 and 68 kilocalories, respectively.
    Zusätzliches Material: 14 Ill.
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  • 21
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 525-526 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A simple method is described for determining absolute turbidities of solutions based on the transmission of light of a highly turbid solution possessing no dissymmetry or depolarization. Stable suspensions of particles of vitreous silica (Ludox) used for this purpose possessed a weight average molecular weight of för millions.
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  • 22
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: In this article only fluid substances are considered, i.e., solutions of macromolecules. It is shown that it is necessary to give several repartition curves of the diffused light intensity in function of the angle and for several concentrations in the aim to obtain the giration-radius of macromolecules and to obtain some data about the interaction potential.
    Notizen: L'article est à peu prèb uniquement consacré aux cas des fluides (solutions de macromolécules par exemple). Il est montré qu'il est nécessaire de conuaître plusieurs courbes de répartition de l'intensité du rayonuement diffusé en fonction de l'angle, relatives à plusieurs concentration de la matière, pour obtenir le rayon de giration des macromolécules et des renseignements sur leur potentiel d'interaction.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 23
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 553-556 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polyvinylpyrrolidone (PVP) shows ultraviolet maxima which may be attributed to the presence of pyrrolidone rings and to unreacted vinyl groups. The spectrum is considerably altered at extreme values of pH. Complex formation between PVP and molecular iodine was examined by following alterations in spectra of the iodine. Dyes bound to PVP show altered spectral and photochemical properties from that of the free dye.
    Materialart: Digitale Medien
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  • 24
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 476-478 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 25
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: We have studied the copolymerization behavior of perfluoropropene, perfluorobutene-1, perfluorobutene-2, perfluoroisobutene, perfluoropentene-1, and perfluorononene-1. We have so far not succeeded in homopolymerizing these olefins. However, certain nonfluorinated, nonconjugated comonomers-ethylene, vinyl. chloride, vinyl acetate, and the vinyl alkyl ethers-were found to copolymerize readily, giving copolymers containing up to 50 mole per cent, and in some cases slightly more than this, of the perfluoro-olefin in the copolymer. The higher members of the series copolymerize in general less readily than the lower members. The products ranged from viscous oils to tough, film-forming solids. The difficulty of homopolymerization and the relative ease of copolymerization of the perfluoro-olefins with the above comonomers are discussed and interpreted in terms of probable electron distributions around the double-bond.
    Zusätzliches Material: 5 Tab.
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  • 26
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Some physical properties of solutions of sodium thymonucleate in neutral solution and after adjustment to pH 3.8 with 0.01 M HCl have been determined. It is found that the intrinsic viscosity at zero gradient is 5700 in neutral and 3900 at pH 3.8. Moreover, the latter viscosity remains unchanged upon reneutralizing the solution with 0.01 M NaOH. Light scattering shows that the molecular weight is the same in both cases and indicates that the particles are more anisodiametric in neutral solution. Streaming birefringence and extinction angle measurements are interpreted as supporting this view.
    Notizen: Certaines propriétés physiques des solutions de thymonucléte sodique ont été déterminées en solution neutre et après ajustement au pH 3.8 au moyen d'acide chlorhydrique 0.01 M. On a trouvé que la viscosité intrinsèque au gradient zéro est 5700 en solution neutre et 3900 au pH 3.8. De plus, cette dernière viscosité reste inchangée après reneutralisation de la solution avec de la soude 0.01 M. La diffusion de la lumière montre que le poids moléculaire est le même dans les deux cas, et indique que les particules sont plus dissymétriques en solution neutre. Des mesures de biréfringences d'- écoulement et d'angles d'extinction permettent de confirmer cette interprétation.
    Zusätzliches Material: 5 Ill.
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  • 27
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Recent advances in the techniques and theories of low-angle x-ray diffraction are critically analyzed from the point of view of the practical possibilities they offer in the investigation of macromolecules and micelles.
    Notizen: Les progrès récents réalisés dans la technique et dam les différentes théories de la diffraction des réactions-X à faible angle sont analysés de façon critique en vue d'examiner les possibilités pratiques qu'ils offrent dans les recherche sur les macromolécules et les miceues.
    Materialart: Digitale Medien
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  • 28
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 579-581 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 29
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 588-592 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 30
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 593-593 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 31
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 395-407 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: (1) Sebacamide and N,N′-diacetylhexamethylenediamine interchange to produce acetamide and polyhexamethylene sebacamide. (2) The rate is proportional to the concentrations of the two reacting species and to the square root of carboxyl group concentration. (3) The rate increases with increasing concentration of water. Reagents which had been held in the molten state under high vacuum were still capable of reaction. (4) N-Substitution decreases the rate constant; the isobutyl group is more effective than methyl in this respect. (5) As an indication of the amount of interchange occurring during a typical polymerization, it is computed that at least 42% of the amide links interchange during the 66 nylon synthesis. This means that it is not feasible to make nonrandom copolyamides by polymerizing together low molecular weight homopolyamides. Interchange does provide for the production of nonrandom copolymers from two or more high molecular weight homopolyamides.
    Zusätzliches Material: 3 Ill.
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  • 32
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 444-444 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 33
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 446-447 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
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  • 34
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 448-448 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 35
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 476-476 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 36
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 495-502 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Some copolymers which contain either aldehyde or ketone carbonyl groups have been treated with phosphorus trichloride and then in sequence with acetic acid and water. On the basis of phosphorus analyses of the resulting products, α-hydroxyphosphonic acid groups have been introduced in amounts ranging from zero to 100% of the theoretical amount. These phosphorus containing polymers with 2% or more of phosphorus are somewhat flame resistant.
    Zusätzliches Material: 4 Tab.
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  • 37
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 503-518 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A review of the data available in the literature and new data reported in this paper show that in any homologous series of condensation polymers there is a uniform change in the melting point as the hydrocarbon content of the polymer is increased. If all such series are treated as copolymers of the simplest modifying element and polyethylene and the composition expressed on a mole fraction basis, the data when presented graphically show that the melting points of any such series passes through a minimum at some intermediate composition. The position of the minimum as well as the depth of the minimum is dependent on the polarity of the modifying group. This survey has included aliphatic polyesters, aromatic polyesters, polysulfides, cellulose derivatives, and polyamides. Some of the series are complete enough to show a definite minimum with compositions on either side of the minimum with higher melting points. In some compositions based on the very highly polar groups, such as amides, the series is not complete enough to establish the complete shape of the curve, but the indications are strong that the minimum does exist.
    Zusätzliches Material: 2 Ill.
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  • 38
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 7 (1952), S. 274-293 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Les polyisobutylènes macromoléculaires (Oppanole) se comportent dans les bons solvants p. e. dans le cyclohexane comme les produits à macromolécules linéaires. Dans le mauvais solvant benzène ils sont à 20° l'attitude des sphérocolloïdes. Selon les idées de W. Kuhn c'est dû au reploiement des macromolécules en forme de pelote causé par une association intramoléculaire. A 60° les macromolécules se déplient et s'étendent, et de cette manière ces solutions des polyisobutylènes dans le benzène deviennent semblables à celles des colloïdes linéaires.
    Notizen: Die hochpolymeren Polyisobutylene (Oppanole) verhalten sich in guten Lösungsmitteln, wie Cyclohexan, wie linearmakromolekulare Stoffe; in dem schlechten Lösungsmittel Benzol zeigen sie dagegen bei 20° das Verhalten von Sphärokolloiden. Entsprechend Anschauungen von W. Kuhn ist dies auf eine starke Zusammenfaltung der Makromoleküle zu Knäueln durch intramolekulare Assoziation zurückzuführen; bei 60° tritt eine Streckung der Makromoleküle ein, so daß sich dann die Benzollösungen der Polyisobutylene wie die von Linearkolloiden verhalten.
    Zusätzliches Material: 9 Ill.
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  • 39
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 7 (1952), S. 236-258 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: The molecular weights of PVP fractions determined by means of the osmotic pressure confirm the formula M̄w = 15 K2, 3 for a molecular range of 10 000 to 100 000. - For PVP samples of higher molecular weight too low values have been found because of the inhomogeneity of the fractions.For unfractionated samples the average molecular Weight can be calculated with the Fikentscher k-values by means of the approximated formula M̄n = 24 k2.The permeability of the membranes to PVP molecules was found by test to be negligible only above M ≧ 10 000.When a PVP fraction is taken as a standard, the molecular weights determined by light scattering agree fairly well with those found by ultracentrifuge measurements, confirming in particular the validity of the formula Zη = 1,4 · 10-5 M0.70 also for the range of higher molecular weights.Using light scattering measurements as a function of were length and assuming that the molecules are of a random coiled form, the following mean square molecular diameters have been determined: \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l}360 \hbox{\AA}\ \hbox{for M = 249 000 and} \\ 930\hbox{\AA} \hbox{ for M = 1 116 000}\end{array}$$\end{document} corresponding to very tightly coiled molecules of PVP in aqueous solution.
    Notizen: Bei der Bestimmung des Molekulargewichts von PVP-Fraktionen mittels des osmotischen Drucks erhält man Werte, die die in der vorausgehenden Arbeit von Scholtan Angegebenen Formeln im Molekulargewichtsbereich von 10 000 bis 100 000 bestätigen. Für PVP mit höherem Molekulargewicht werden allerdings infolge der Uneinheitlichkeit der Fraktionen zu kleine Werte gefunden.Für unfraktionierte Produkte gilt für die Berechnung des Zahlenmittels des Molekulargewichts aus den k-Werten nach Fikentscher die Näberungsformel M̄n = 24 k2.Die Prüfung der verwendeten Membranen auf ihre Durchlässigkeit für PVP-Moleküle ergibt, daß nur für M ≦ 10 000 mit einer nicht zu vernachlässigenden Diffustion zu rechnen ist.Die aus den Lichstreuungsmessungen ermittelten Molekulargewichte stimmen bei der Wahl einer PVP-Fraktion als Standardsubstanz ziemlich gut mit den aus den Ultrazentrifugen-Messungen ermittelten Werten überein. Sie bestätigen insbesondere die von Scholtan angegebene Formel auch für höhere Molekulargewichte.Aus der vom Rayleighschen Gesetz abweichenden Wellenlängenabhängigkeit der Streuintensitäten für 2 Höhere molekulare PVP wird unter Annahme eines Kuhnschen Knäuelmodells der statistische Abstand der Molekülenden, also der angenäherte Knäueldurchmesser, für M = 249 000 zu 360 Å und für M = 1 116 000 zu etwa 930 Å ermittelt. Die PVP-Moleküle sind in Wäßriger Lösung also start geknäuelt.
    Zusätzliches Material: 6 Ill.
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  • 40
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 7 (1952), S. 320-327 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Pour expliquer le procédé du tannage on a measuré l'adsorption des matières tannantes sur des polyamides définés (Igamid 6A) comme substance-modèle pour kollagène et sur de la peau pulvérisée. Par report au contenu d'azote les deux substances montrent des courbes d'adsorption presque identiques. Sous certaines conditions il a été possible de faire sortir par lavage l'extrait de bois de québracho qui a été utilisé comme matière tannante. Ce qui montre qu'elle n'est pass liée à l'Igamid ou à la peau par des valences principales. Le tannage consiste alors dans I'adsorption des matières tannantes aux liaisions peptidiques du kollagéne. On peut done la comprendre comme transfert du kollagène “plastifié” par l'eau dans un kollagène “plastifié” par la matière tannante, c'est à dire comme plastification déhydratisante.
    Notizen: Um den Gerbvorgang zu erklären, werden an definierten Polyamiden (Igamid 6A) als Modellsubstanz für Kollagen und an Hautpulver Gerbstoffadsorptionen Gemessen. Bezogen auf ihren Stickstoffgehalt, zeigen beide Substanzen nahezu identische Adsorptionskurven. Der zur Gerbung verwendete Quebracho-Gerbstoff läßt sich unter bestimmten Bedingungen wieder auswaschen, ist also nicht durch Hauptvalenzen an Igamid oder Haut gebunden. Gerbung wird demnach durch Adsorption der Gerbstoffe an den Peptidbindungen des Kollagens bedingt; sie kann als eine Überführung des mit Wasser “weichgemachten” Kollagens in ein mit Gerbstoff “weichgemachtes” Kollagen, also als eine dehydratisierende Weichmachung aufgefaßt werden.
    Zusätzliches Material: 1 Ill.
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  • 41
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 7-20 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Spectrographic studies on the hydrolysis of human tendinous collagen by means of pepsin, pancreatine and HCl show that the absorption of the present chromophorous amino-acids contributes only a small share to the total absorption of the collagen between 2500 and 4200 mm-1. The considerably greater part of this total absorption is ascribed to H-bonded peptide groups, either in the keto- or in the enolic form, depending on the pH-value. Analogous absorption bands could be observed with N-methylacetamide at corresponding pH-values. On the basis of these results, it can be demonstrated that the fermentative hydrolysis - like the reaction with cupri-ethylen-diamine-leads to a cleavage of the H-bonds, whereas the HCl-hydrolysis results also in a considerable proteolysis. The absorption of gelatine leads to the conclusion that there are much less H-bonds as compared to the native collagen.
    Notizen: Spektrographische Untersuchungen über die fermentative und Säure-Hydrolyse von menschlichem Sehnenkollagen zeigten, daß die Aminosäure-Absorption nur einen kleinen Teil der Gesamtabsorption von Kollagen im Gebiet zwischen 2500 und 4200 mm-1 ausmacht. Der weitaus größere Anteil wurde H-gebundenen Peptidgruppen zugeschrieben, die  -  je nach dem pH-Wert des Quellungsmittels  -  in der Keto- oder Enolform existieren können.Ganz analoge Absorptionsbanden kann man auch bei N-Methylacetamid bei den entsprechenden pH-Werten beobachten.Auf Grund dieser Ergebnisse kann gezeigt werden, daß der Fermentabbau ebenso wie die Reaktion mit Cupriäthylendiamin im wesentlichen nur zu einer Sprengung der Wasserstoffbrücken führt, die Säurehydrolyse dagegen auch zu einer beträchtlichen Proteolyse. Die Absorption der Gelatine ergibt, daß hier bedeutend weniger H-Brücken vorhanden sind als beim nativen Kollagen.
    Zusätzliches Material: 5 Ill.
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  • 42
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 85-97 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: The polycondensation (hardening) of p-cresol dialcohol, performed in platinum or silver vessels and crucibles, is the same and depends mainly on the purity of p-cresol dialcohol. The rate of condensation in air is different from that in nitrogen. The volume or the vertical dimension of the dialcohol to be melted also effects the rate of hardening. Characterisation of the condensation by the loss of weight of the melting (in combination with the analysis of the formaldehyde) is only possible by careful drying of the condensation products at low temperatures. Sometimes the loss of weight during drying attains the same amount reached immediately after condensation. Under these conditions the hardening of the p-cresol dialcohol is reproducible.It is even possible to condense the purest p-cresol dialcohol at 130°C so that within seven hours the loss of water nearly amounts one mol and that of formaldehyde at most only to 0,008 mol formaldehyde pro mol phenol alcohol.The kinetics of the condensation, at which almost only water is lost, is mathematically given by p (ratio of reacted to unreacted methylol groups) and experimentally by the loss of weight during the condensation.The hardening of p-cresol dialcohol in the solid state is at least partially possible.
    Notizen: Die Polykondensation (Härtung) des p-Kresoldialkohols, die in Platin- oder Silbergeräten ausgeführt wird, zeigt übereinstimmenden Verlauf und ist abhängig von der Reinheit des p-Kresoldialkohols. Die Geschwindigkeit der Kondensation ist verschieden unter Luft und Stickstoff. Ebenso zeigt das Volumen der Schmelze bzw. deren Schichthöhe einen Einfluß auf die Härtungsgeschwindigkeit. Verfolgt man die Kondensation durch den Gewichtsverlust (in Verbindung mit Formaldehydbestimmungen), so ist die Trocknung der Kondensate besonders zu beachten; der Trocknungsverlust nach der Kondensation kann den Gewichtsverlust unmittelbar nach der Härtung erreichen. Bei Einhalten der angegebenen Kondensationsbedingungen ist die Härtung des p-Kresoldialkohols eindeutig reproduzierbar.Die Kondensation reinsten p-Kresoldialkohols bei 130°C kann derart durchgeführt werden, daß innerhalb 7 Stunden nahezu 1 Mol Wasser neben höchstens 0,008 Mol Formaldehyd je Mol Phenolalkohol abgespalten wird.Die Kinetik der Kondensation, bei der praktisch nur Wasser abgespalten wird, ist mit Hilfe des Begriffes p (Verhältnis der umgesetzten zu den umsatzfähigen Methylolgruppen) und experimentell durch den Gewichtsverlust bei der Härtung verfolgbar.Eine Härtung des p-Kresoldialkohols im festen Zustand ist mindestens teilweise möglich.
    Zusätzliches Material: 4 Ill.
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  • 43
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Nous discutons la forme des molécules de polyesters correspondants substitués et non substitués d'aprés la méthode de titrage par précipitation et à l'aide de la fonction Zη(P). Un procédé de calcul simple des éléments de chaine statistiques, qui se base sur une synthése des théories de W. Kuhn et H. Kuhn et de P. Debye et A. M. Bueche fournit un élément de chaine plus long pour les polyesters substitués. Les polyesters substitués possédent done une structure plus lâche. Dans les deux types de polyesters nous trouvons un certain accroissement de l'élément de chain statistique avec le Degré de polymerisation, que nous discutons en detail. Ni les résultats expérimentaux ni des considérations (basés sur la variation de l'élément de chaine statistique) ne permettent d'affirmer l'éxistence de branches latérales.
    Notizen: Es wird die Molekülgestalt bei sich entsprechenden nichtsubstituierten und substituierten Polyestern nach der Methode der Fällungstitration und mittels der Zη(P),-Funktion untersucht. Ein einfaches Verfahren zur Berechnung der statistischen Fadenelemente, das auf einer Verknüpfung der Theorien von W. Kuhn und H. Kuhn von P. Debye und A. M. Bueche beruht, liefert für die substituierten Polyester das größere statistische Fadenelement. Substitutierte Polyester besitzen demanch die gedehntere Gestalt. Bei heiden Polyestertypen wird eine gewisse Zunahme des statistischen Fadenelementes mit dem Polymerisationsgrad gefunden, die eingehender diskutiert wird. Für das Vorliegen von Verzweigungen sprechen weder die experimentellen Ergebnisse noch theoretische Überlegungen, die auf Ground der Inkonstanz der statistischen Fadenelemente angestellt werden können.
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  • 44
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 156-177 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: In the hydrolysis of polysaccharids with sulphuracid of 70-75 weight % in a closed vessel all reactions which pass under lieing on water or elimination of water effect a change of the concentration of acid. This change of the concentration and with that passing of reaction was registering followed by measurement of conducting power by means of an apparatus for this constructed specially.After gauging of the apparatus with known substances was comparing examined untreated wood of beech, such after alkaline and acid treatment, also the residue which is resistent to chlordioxyd (ClO2).It was found, that the native lignin eliminated water as well as lied on during the total-hydrolysis. The quantity of eliminated and lied on water has the relation 3:1. The elimination of water partially happens on conditions how they are usual at the partial-hydrolysis of the wood. The whole eliminated condensation-water out of the native lignin of the analysed heechwaod amounts 2,9-3,1% of the wood. For this amount the contents of lignin are lower. In summary-analyses one has to regard.Earlier findings are veryfied, that one part of the native lignin is resistent to ClO2. This ligninfragment is the support of the eliminating groups whilst the lieing on of water happens on the aromatic components of the lignin.
    Notizen: Bei der Hydrolyse von Polysacchariden mit Schwefelsäure von 70-75 Gew.% in einem geschlossenen Gefäß bewirken alle unter Wasseranlagerung oder Wasserabspaltung verlaufenden Reaktionen eine Änderung der Säurekonzentration. Diese Konzentrationsänderung und damit der Reaktionsverlauf wurde durch Leitfähighkeitsmessung mittels einer hierfür entwickelten Apparatur registrierend verfolgt. Nach Eichung des Gerätes mit bekannten Substanzen wurde unbehandeltes Buchenholz, solches nach alkalischer und saurer Vorbehandlung sowie der gegen Chlordioxyd resistente Rückstand des Holzes vergleichend untersucht.Es wurde festgestellt, daß bei der Totalhydrolyse das native Lignin sowohl Wasser abspaltet wie auch anlagert. Die abgespaltene und angelagerte Wassermenge verhält sich view 3 : 1. Die wasserabspaltende Reaktion findet teilweise bereits unter Bedingungen staff, wie sie bei der Vorhydrolyse des Holzes gebräuchlich sind. Das insgesamt aus dem nativen Lignin der untersuchten Buchenholzprobe abgespaltene Kondensationswasser beträgt 2,9-3,1% des Holzes. Um diesen Betrag wird der Ligningehalt zu niedrig gefunden, was bei der Summenanalyse der Holzprobe zu berücksichtigen ist.Es bestätigten sich frühere Befunde, denen zufolge ein Teil des nativen Lignins gegen Chlordioxyd beständig ist. Dieses Ligninfragment is der Träger der wasserabspaltenden Gruppen, Während die Wasseranlagerung an der aromatischen Komponente des Lignins vor sich geht.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 45
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 217-251 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: On a préparé des polyesters de I'hexandiol avec les acides sucinique, maleique et fumarique. La relation entre Zη (nombre de viscosité) et le nombre de chaînons est une équation exponentialle, dans laquelle, pour un même solvant, la puissance la plus élevée se rapporte aux polyesters de I'acide fumarique. La valeur qui correspond aux polyesters de I'acide succinique est un peu plus faible. Pour les polyesters de I'acide maleique elle est beaucoup plus faible.Comme preuve de la structure, on a utilisé I'hydrogénation des polymères analogues des polyesters de I'acide succinique et la transformation des polyesters de I'acide maleique en polyesters de I'acide fumarique.
    Notizen: Es wurden Polyester aus Hexandiol mit Bernsteinsäre, Maleinsäure und Fumarsäure hergestellt. Der Zusammenhang zwischen Viskositätszahl und Kettengliederzahl entspricht einer Potenzgleichung, wobei im gleichen Lösungsmittel die Polyester mit Fumarsäure den höchsten Exponenten haben. Der entsprechende Wert für Polyester mit Bernsteinsäure ist etwas niebriger, während die Polyester mit Maleinsäure einer sehr viel niedrigeren Exponenten zeigen.Als Strukturbeweis wurden die polymeranaloge Hydrierung zu Polyester mit Bernsteinsäre und die Umlagerung von Polyestern mit Maleinsäure zu solchen mit Fumarsäure herangezogen.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 46
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 353-364 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Direct determinations of the number average molecular weights of a variety of British and American polythenes have been made making use of two experimental techniques: (1) ebulliometry and (2) high temperature osmometry. An intrinsic viscosity-molecular weight relation has also been obtained which covers the range 1.3 × 103 to 76 × 103 and includes representative samples of Alkathene. The Huggins constants k' and μ have been evaluated from viscosity and osmotic pressure data and their bearing on polythene structure discussed.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 47
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 371-394 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Die Kondensationsreaktion von Harnstoff und Formaldehyd wurde für ein Molarverhältnis 1:1 und 1:2 beider Komponenten untersucht; die Reaktion verläft immer nach der zweiten Ordnung. Dies Reaktionen wurden mit den Kondensationen von reinem Mono- und Dimethylolharnstoff verglichen und mit ihnen analog befunden. In neutraler Lösung bei Messungen bei 65, 75 und 85° war der erhaltene Wert der Aktivierungsenergie 21 Kal./Mol für beide Reaktionen; die Kondensationsreaktion im Verhältnis 1:2 ist jedoch drei Mal langsamer als die Kondensation 1:1. In saurer Lösung wurde gefunden, dass eine rein saure katalytische Wirkung auftritt, und die Reaktionsgeschwindigkeiten zwischen pH 3 und pH 5 waren der Wasserstoffionenkonzentration proportionell; die Aktivierungsenergie wurde für die saure Kondensationsreaktion zu ungefähr 8-10 Kal. abgeschätzt. Bei höheren pH Werten treten beide Reaktionen, die thermische und die Säure-katalysierte, zusammen auf, und der Exponent der Wasserstoffionenkonzentration in dem Ausdruck der Kondensationsgeschwindigkeit wird kleiner als die Einheit. Es werden analytische Bestimmungen der Kondensationsprodukte gegeben, und ein wahrscheinliches kinetisches Schema der Reaktionen wird angegeben.
    Notizen: The condensation reaction of urea and formaldehyde was studied in a molar ratio 1:1 and 1:2 of both components; the reaction always proceeds by a second-order mechanism. These reactions were compared and found analogous to the condensations of pure mono- and dimethylolurea. In neutral medium, by measuring at 65, 75, and 85° the value obtained for the energy of activation was 21 kcal./mole for both reactions; the 1:2 ratio-condensation reaction is nevertheless three times slower than the 1:1 condensation. In acidic medium, a pure acid catalytic effect was found to be true, and the rates of the reaction between pH 3 and pH 5 were proportional to the hydrogen-ion concentration; the activation energy was evaluated at about 8-10 kcal. for the acidic condensation reaction. At higher pH values, both reactions, thermal and acid-catalytic, occur together, and the exponent to the hydrogen-ion concentration in the expression of the rate of condensation appears to be smaller than unity. Analytical determinations of the condensation products are given and a likely kinetic scheme for the reaction is indicated.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 48
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 425-434 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Interpretations of the small-scale structure of natural cellulose have been greatly influenced by information obtained from x-ray diffraction studies. This work has given rise to a structural model, according to which there are some regions of cellulose in which the molecules are highly ordered (crystalline) and other regions in which there is considerable disorder (amorphous). This interpretation does not, however, adequately emphasize the fibrillate character of natural cellulose-a structure which, as the result of light and electron microscope investigations, is well established. Since many reactions proceed more readily in the interfibrillar regions than in the fibrils themselves, it seems that the cellulose molecules in the fibrils, in contrast to those in the interfibrillar regions, are more highly ordered. Intensive treatments, such as acid hydrolysis, may cause a further breakdown whereby the fibrils are split transversely into small rodshaped particles, but the comparatively greater ease with which fibrillation occurs following a variety of degradative reactions suggests that the ordered character of the fibrils along the long axis is not interrupted by regions of the same magnitude and extent of disorder as those which occur between the fibrils. Although x-ray diffraction diagrams of cellulose have generally been considered to indicate the presence of small elongated regions of highly crystalline cellulose, i.e., micelles, it would be equally consistent to suppose that the diffuse diffraction patterns were caused by larger essentially homogeneous regions in which the arrangement of the molecules only approximates crystalline regularity. These regions which, except for occasional grosser irregularities, have a more or less uniform intermediate molecular order, may be identified with the fine electron microscopically visible fibrils. According to this viewpoint highly ordered micelles, unlike fibrils, are to be regarded more as incidental rather than as fundamental units of cellulose structure.
    Materialart: Digitale Medien
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  • 49
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 457-465 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Light scattering and ultracentrifuge experiments were made on iodinated fibrinogen. The molecular weight was found to be 560,000 and the length 900 A. The experiments on polymerized iodo-fibrinogen indicated that the lateral and end-to-end associations have different pH optima.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 50
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 528-528 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 51
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 621-632 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: For a soft free-draining coil that changes its shape quite easily in flow, intrinsic viscosity does not depend on velocity gradient. The deformation and extension of the coil in flow, which increases the contribution of the single molecule, is just compensated for by the decrease in number of molecules crossing the flow plane and thus actually contributing to the additional shear stress. The finite valence angle and the restricted rotation around the valence bond, however, not only extend but also stiffen the molecule. The completely stiff coils - an idealization that never occurs but is very suitable for computing purposes - are oriented in the flow without any alteration of their shapes and shape distribution. The intrinsic viscosity thereby decreases with increasing orientation. The effect is the more accessible the longer the molecule, the deviations from the initial viscosity at rest being proportional to the square of the gradient and the fourth power of the degree of polymerization. The real molecules are neither quite stiff nor completely soft. Thus their intrinsic viscosity ought to lie between the two limiting cases, the decrease with the gradient being smaller than for the stiff coils. Taking into account the hydrodynamic interaction of the chain elements, the gradient dependence cannot be computed precisely. Qualitative considerations yield an increased viscosity contribution with the stretching of the coils, since they become more permeable the more they are extended. Thus the intrinsic viscosity of quite soft molecules should increase with the gradient. In completely stiff coils, however, the partial solvent immobilization does not change the gradient dependence, on the whole, since the shapes and the shape distribution are unaltered by the flow, although the appearing of the effect is displaced to higher gradients, and the absolute value of the initial intrinsic viscosity is very markedly reduced. Experiments are too rare and not sufficiently precise to allow any reliable test of the theory. In most cases, the concentrations and the gradients are too high for an unambiguous extrapolation to infinite dilution and zero gradient viscosity. But they nevertheless seem to exclude the case of quite soft molecules and are not in contradiction with the general features of the theory.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 52
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 651-656 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 53
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 69-71 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The theory of molecular distribution in condensation polymers has been extended to include systems of a rather general type. Equations for the distribution and the weight-average molecular weight are given.
    Materialart: Digitale Medien
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  • 54
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 93-95 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 55
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 96-96 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 56
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 97-113 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: It has been determined analytically that, when a Butyl vulcanizate softens during exposure to high temperature, the disulfide cross links between polymer chains break down to thiol groups. Of all the accelerator types, tellurium derivatives of dithiocarbamic acids impart the greatest inherent resistance to this reversion. Such a mechanism of breakdown, however, suggested the use of oxidizing agents to reform the disulfide cross linkage, and four metallic peroxides or dioxides have been found effective. These are CaO2, PbO2, MnO2, and SrO2. Barium peroxide is too stable to be an effective oxidizing agent while magnesium peroxide expels oxygen too rapidly for an effective retarder. Other types of organic and inorganic oxidizing agents have not proved beneficial. The fact that an oxidizing action is responsible for retardation of reversion has been demonstrated by the fact that the corresponding mono-oxides of calcium, strontium, lead, and manganese do not perform in the same manner. In rubber technology the stabilization of vulcanized materials by oxidizing agents is novel, and it appears applicable only in the case of Butyl whose low unsaturation offers greater resistance to oxidation of the chain proper. When CaO2 is added to diene type rubbers such as Buna S, Buna N, and natural rubber the common oxidative effects are accelerated. With the Buna rubbers the hardening action is more rapid, while with natural rubber a softening followed by a hardening action is promoted.A practical illustration of this principle of retarding reversion of Butyl vulcanizates by oxidizing agents has been presented. It has been demonstrated in the laboratory that the service life of automotive tire curing bags made from Butyl can be prolonged by the addition of these metallic dioxides or peroxides to the compound.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 57
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 170-170 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 58
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In Part I the translational resistance of the random coil was discussed. In the two limiting cases of the freely draining and the completely nondraining coil a theoretical treatment was given, while for intermediate draining conditions an experimental method, involving large-scale models of the molecules, was shown to be available. The same treatment is now extended to deal with the analogous case of the hydrodynamic rotational resistance of the random coil. It is on this characteristic resistance that the intrinsic viscosity and the flow birefringence of solutions of chain molecules principally depend.Expressions are found for the viscosity index [η], the orientation index [ω], and the birefringence index [n], respectively. In these formulas Z is the degree of polymerization while the parameters aη, aη, aη, and brot are independent of Z. These parameters are, however, functions of the length Am of the preferential statistical chain element and the hydrodynamic thickness dh of the chain. an also includes the anisotropy of polarizability of the statistical chain element. It is seen moreover that [ω] (in contrast to [η] and [η]) also depends on the shape resistance of the chain (i.e., on the resistance which the chain inherently offers to a rapid change in configuration).
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
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  • 59
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 61-68 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The formation of “grafted” vinyl copolymers by polymerizing one monomer in the presence of a preformed vinyl polymer has been extended to a new monomer-polymer combination and one point of attachment of the lateral (grafted) polymer chain has been shown precisely. When ethylene was polymerized in the presence of polyvinyl acetate under a variety of conditions, modified polyvinyl acetates having lateral polyethylene chains were formed. Alkaline methanolysis of such modified polymers yielded mixtures of long-chain fatty acids and ethylene-modified polyvinyl alcohols (which were inseparable from any unmodified polyvinyl alcohol that may have been present). The hydrolysis to long-chain acids shows that polyvinyl acetate acts as a chain transfer agent and that one point of lateral growth of polyethylene chains is the —CH3 in the acetoxy group of polyvinyl acetate. The second hydrolysis product, the ethylene-modified polyvinyl alcohol, shows that chain transfer, and subsequent growth of polyethylene chains, can also occur on the chain carbons of polyvinyl acetate. Oxidation of the ethylene-modified polyvinyl alcohols yielded a mixture of oxalic acid and long-chain fatty acids. At the low ethylene pressures studied (300 to 1200 p.s.i.) only traces to small amounts of low molecular weight polyethylene waxes were formed.
    Zusätzliches Material: 5 Tab.
    Materialart: Digitale Medien
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  • 60
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The optimum pH for the emulsion polymerization of hexamethylenedithiol and diallyldimethylsilane was found to be in the region of 3.0 to 4.0. A variety of polyalkylene sulfides containing silicon were prepared using bulk, solution, and emulsion polymerization techniques. All of the polyalkylene sulfides which contained silicon were heavy oily materials which were very “tacky”.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 61
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 657-657 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 62
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 41-52 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The elasticity of polythene melts was measured with a resonance method by inducing shear oscillations in the region about 30 cycles/second at small shear amplitudes. The experiments covered a temperature region of 130° to 230°C. and a range of (osmotic) molecular weights from 12,000-64,000. Shear moduli of the order 105 to 105 dyne cm.-2 were observed and a single relaxation time appeared sufficient to characterize the mechanical behavior of the polythene melts at a given temperature. The variation of mechanical parameters with temperature and molecular weight is brought into relation with known data on the amount of chain branching.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 63
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Aqueous alkali has been assumed to be a good solvent for amylose, and has been used as a medium for physicochemical studies on this polymer. It is shown that there is a slow but substantial reduction in the turbidity of normal KOH solutions of amylose, even in the almost total absence of oxygen. More significantly there is a corresponding, but much more rapid, drop in turbidity in neutral solutions (pH 6.5-7.0). At pH 4.0 the turbidities are, in general, constant for up to at least 30 days. The results are interpreted on the basis of aggregates, which evidently must be of a very special type and are termed “native” aggregates. It is suggested that these may consist of amylose in essentially the helical configuration. The properties of these aggregates are in strong contrast to those of the retrograded aggregates. In the form of the first type of aggregate the amylose will not retrograde, at room temperature, without undergoing first a drop in turbidity suggesting that the transition from the “native” to the retrograded aggregate passes through the molecular state. The native aggregates are stabilized toward both disaggregation and retrogradation by pretreatment with iodine. Disaggregation is accompanied by a drop in relative viscosity. Some of the implications of these unexpected observations are pointed out.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 64
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Decreases in particle weight of amylose on aging in neutral and in alkaline aqueous solution are demonstrated by measurements of turbidity as a function of concentration. This further verifies that the previously reported turbidity drops are a consequence of disaggregation of an unusual type of aggregate. The same particle weights are obtained, in the case of aggregated samples, at pH 4 and in normal KOH. Anomalies arise in dilution series carried out in neutral solution and in solutions at pH 4 in the case of amyloses of low degree of aggregation, and a probable explanation is given. Samples can be partially stabilized in a given state of disaggregation by rendering the solution alkaline, and normal dilution series curves result. Disaggregation of the “native” aggregates continues along with retrogradation, and the retrograded aggregates are broken down readily by alkali. This leads to a method of disaggregation based on retrogradation followed by solution in 0.5 N KOH.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 65
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In applying the quadratic form π/c = (π/c)0[1 + Γ2c + Γ3c2] to osmotic pressure of dilute polymer solutions, the use of a third coefficient (Γ3), which is related semitheoreti-cally to the second (Γ2), is to be recommended over the use of unrestricted coefficients, both from the standpoint of expediency and of accuracy in the values so obtained for the intercept (π/c)0. and the initial slope (π/c)0Γ2.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 66
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 23-33 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A light scattering investigation of actin and actomyosin gives the following information. The weight average molecular weight of 80,000 is found for G-actin. The average molecular weight and length of F-actin decrease upon increasing concentration of electrolyte, the effect being especially pronounced in the case of KI. The average molecular weight and length of F-actin decrease with increasing of pH of polymerization. The average length and molecular weight of F-actomyosin increase with decreasing ionic strength. The average length and molecular weight of F-actomyosin decrease with decreasing size of the F-actin component.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 67
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 63-72 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: (1)The reactivity of monomers in an ionic copolymerization is shown to be a function of the polarity of the substituent on the ethylenic double bond.(2)The nonalternating tendency is explained by the absence of an alternating polar effect during the propagation step.(3)The results seem to indicate in the case of the monomers studied here the absence of any other selective effects (e.g., steric) and furthermore that the reactivity of the carbonium ions derived from these different monomers is the same. Therefore it is suggested that:(4)The original Wall equation, dM1/dM2 = α(M1/M2) may be applied.
    Zusätzliches Material: 1 Ill.
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  • 68
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 73-90 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: This paper is concerned with the description of a simple technique for determining the molecular weight distribution curve of polystyrene (and presumably any other soluble polymer consisting of a polymer-homologous series). The general theory of the method as well as preliminary experimental results will be covered. The method is characterized by: (1) simple technique and equipment; (2) no need to isolate and measure fractions; and (3) a general basis in thermodynamic theory of polymer solutions, although a double calibration is needed to determine numerical parameters. The method consists in adding increasing quantities of nonsolvent to a dilute solution of polystyrene in a good solvent and observing the cumulative volume of precipitate as a function of nonsolvent content. The settled gel must re-equilibrate (hence deswell) with the new solvent after each alcohol addition. The swelling ratio, S (cc. of swollen gel per gram of dry polymer), of the swollen precipitate is approximately independent of the molecular weight and depends mainly on the volume percent of nonsolvent, γ according to (1)\documentclass{article}\pagestyle{empty}\begin{document}$ \gamma {\rm } = {\rm }\alpha + {\sigma \mathord{\left/ {\vphantom {\sigma {\left( {S^S } \right)}}} \right. \kern-\nulldelimiterspace} {\left( {S^S } \right)}} $\end{document} where α, σ, and s are constants. Likewise, the molecular weight, M, of the species precipitated at any nonsolvent content is given by the Schulz precipitability equation: (2)\documentclass{article}\pagestyle{empty}\begin{document}$ \gamma {\rm } = {\rm }\alpha + {\beta \mathord{\left/ {\vphantom {\beta {\left( {M^m } \right)}}} \right. \kern-\nulldelimiterspace} {\left( {M^m } \right)}} $\end{document} where α, β, and m are constants. For the system polystyrene-benzene-methanol, we find s = 4/3 while Schulz had already noted that m = 2/3. Elimination of γ and α leads to the prediction of a linear relation between M and S2. A two-fold calibration to obtain the constants in equations (1) and (2) is necessary to convert the observed data to an absolute cumulative weight versus molecular weight curve. However, even the simple plot of cc. of precipitate versus percent nonsolvent is informative. The relationship of these results to the thermodynamic theories of polymer solutions of Flory, Huggins, Gee, and Scott is outlined. The plot of cumulative volume of precipitate against percent nonsolvent has two characteristic features: an inflection point and a maximum. If the original polymer has a weight distribution function of the Schulz type, i.e., MkM × (1 - k)2, where k is related to the number-average molecular weight, M̄n, through M̄n = M0(1 - k)-1, then it can be shown that the maximum occurs at M̄n while the inflection point occurs at 2.15 M̄n.
    Zusätzliches Material: 8 Ill.
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  • 69
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Cyclopentadiene can be catalytically converted into a deep red polycyclopentadienetrichloroacetic acid adduct (I). Oxidation and hydrogenation experiments show that each repeating unit of (I) contains one double bond. Other observations, including spectroscopic and electrochemical measurements indicate that these double bonds are conjugated, and that this polymerization involves the migration of hydrogen atoms. The kinetics of the formation of (I) are investigated and some results of these measurements, together with those pertaining to the alkaline hydrolysis of (I), make it probable that the initiation step is in acid-catalyzed esterification of the diene and that the final polymer is an ester. Colloid chemical properties of (I) are described.
    Zusätzliches Material: 1 Tab.
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  • 70
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: It is shown that the extent of hydrolysis in a given set of conditions is qualitatively related to the thickness of the rayon skin. This interpretation is preferable to that of relating extent of hydrolysis to crystalline amorphous ratio.
    Zusätzliches Material: 1 Tab.
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  • 71
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A study has been carried out on the emulsion polymerization of butadiene, using the “peroxamine” recipe at low temperatures in an attempt to evaluate the absolute propagation rate, according to the theory of Smith and Ewart, from a determination of the rate of polymerization per particle of latex. Unlike the persulfate-mercaptan system previously reported, the hydroperoxide-polyamine systems show a polymerization rate per particle which is independent of all variables other than temperature. Hence this system behaves according to case 2 of the Smith-Ewart treatment, where the number of free radicals per particle is approximately 1/2. On this basis it is possible to calculate a value for the absolute propagation rate constant for butadiene, as follows: kp = 1.2 × 108 e-9300/RT l./mole/sec. This value in turn leads to an evaluation of the absolute rates of some other reactions involving the butadiene radical, such as cross-linking, chain transfer, and copolymerization. It agrees with the current data on absolute rates for other monomers and with present-day theories concerning the effect of conjugation on radical-monomer interaction.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 72
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 7 (1952), S. 294-319 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Methyl methacrylate is polymerized in different mixtures and the polymerisate is divided into fractions. From 9 samples the sedimentation constants by mean of the ultracentrifuge are measured and the diffusion constants with a new constructed diffusion cell specially fit for organic solvents are destined. The progress in experimental technic allows to obtain the sedimentation and diffusion constants down to very low concentrations, so that extrapolation to zero concentration could be done directly from the measured values.In a range of three orders of magnitude a clear relation between molecular weight and intrinsic viscosity results, which can be represented by Kuhn's formula. It is therefore possible to estimate the molecular weight of fractionated polymeric methyl methacrylates in chloroform according the equation \documentclass{article}\pagestyle{empty}\begin{document}$$\eta = 4,85 \cdot 10^{ - 6} \cdot M^{0,80} \left[ {lit/g} \right]$$\end{document} between M = 104 to M = 107.The values are compared with those from osmotic pressure and light scattering measurements. Good agreement is found under consideration of the different averages gained.
    Notizen: Methacrylsäuremethylester wird in verschiedenen Ansätzen polymerisiert, und die Polymerisate Werden in Fraktionen zerlegt. An 9 Präparaten wird die Sedimentations-konstante mittels der Ultrazentrifuge und die Diffusionskonstante in einer new konstruierten Diffusionszelle gemessen, die sich besonders für organische Lösungsmittel eignet. Auf Grund der Verbesserungen in der Versuchstechnik konnten die Sedimentations- und die Diffusionskonstanten bis zu sehr kleinen Konzentrationen gemessen werden, so daß die Extrapolation zur Konzentration 0 unmittelbar aus den Meßwerten vorgenommen werden konnte.Es zeigt sich in einem Bereich von 3 Größenordnungen ein eindeutiger Zusammenhang zwischen Molekulargewicht und Viskositätszahl Zη, der durch die Kuhnsche Formel dargestellt werden kann. Man kann somit im Bereich von 104 bis 107 Molekulargewichte von fraktionierten Polymethacrylsäuremethylestern in Chloroform nach der Gleichung \documentclass{article}\pagestyle{empty}\begin{document}$$\eta = 4,85 \cdot 10^{ - 6} \cdot M^{0,80} \left[ {lit/g} \right]$$\end{document} viskosimetrisch bestimmen. Die Werte werden mit Messungen des osmotischen Druckes und der Lichtzerstreuung verglichen, wobei sich unter Berücksichtigung der abweichenden Durchschnittswertbildung der verschiedenen Methoden gute Übereinstimmung ergibt.
    Zusätzliches Material: 13 Ill.
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  • 73
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Fondu et en solution on avait préparé des polyesters substitués de l'acide αα′-dibutylsébacique ou ββ′-dibutylsebacique et de l'hexandiol. Grâce aux déterminations du poids moléculaire des fractions des polyesters avec des méthodes différentes, la constitution non ramifiée de ces polyesters fut déterminée. Dans la relation Zη = K · nx, l'exponent x a pour les polyesters substitués un plus grand valeur que pour les polyesters de l'acide sébacique et de l'hexandiol.Les propriétés physiques des polyesters substitués sont communiqués.
    Notizen: In Schmelze und in Lösung wurden substituierte Polyester aus αα′-Dibutylsebacinsäure bzw. ββ′-Dibutylsebacinsäure und Hexandiol hergestellt. An den Fraktionen der Polyester wurde durch Molekulargewichtsbestimmungen nach mehreren voneinander unabhängigen Methoden die lineare, nicht verzweigte Konstitution der untersuchten Polyester sichergestellt. In dem Zusammenhang Zη = K · nx hat der Exponent x für substituierte Polyester einen größeren Wert als bei substituierten Polyester aus Sebacinsäure und Hexandiol.Die physikalischen Eigenschaften der substituierten Polyester werden beschrieben.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 74
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 124-133 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Pectinates and pectates of the following metals were made: Fe, Ag, Zn, Cd, Co, Ni, Cu, Pb, Hg, Cr, Mn. Proof is given, that true metalpectinates and -pectates were obtained by precipitating them from pectin solution or sodium pectate solution with the aid of the respective salt solution of the metal. Their properties, especially their solubility were investigated. Hot Concentrated ammonia solution dissolves the pectinates and pectates completely.
    Notizen: Es wurden die Pektinate und Pektate nachstechender Metalle hergestellt: Fe, Ag, Zn, Cd, Co, Ni, Cu, Pb, Hg, Cr, Mn. Es wird der Nachweis geliefert, daß beim Fällen von Pektin- bzw. Na-pektatlösungen mit Metallsalzlösungen wirkliche Metallpektinate und -pektate erhalten werden. Ihre Eigenschaften, insbesondere ihre Löslichkeit, wurden untersucht. Heiße konzentrierte Ammoniaklösung löst die Pektinate und Pektate vollkommen auf.
    Zusätzliches Material: 5 Tab.
    Materialart: Digitale Medien
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  • 75
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 140-146 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: A method for the quantitative determination of the permeability of membranes for solvents is reported.The permeability number of Ultracellafilter membranes in benzene can greatly be altered by treating with other liquids for one day. In benzene the permeability number decreases in course of time; after exchanging benzene for methanol it increases very rapidly at first and still continues to increase slightly after one week.
    Notizen: Es wird eine Methode zur quantitativen Bestimmung der Durchlässigkeit von Membranen für Lösungsmittel beschrieben.Die Permeabilitätszahl von Ultracellafilter-Membranen in Benzol kann durch eintägige Einwirkung anderer Flüssigkeiten stark geändert werden. In Benzol nimmt die Permeabilitätszahl im Laufe der Zeit ab; sie steigt beim Austausch von Benzol durch Methanol zunächst sehr rasch an und nimmt auch nach einer Woche immer noch schwach zu.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 76
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 182-182 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 77
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 98-109 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: p-cresol dialcohol, which is free from sodium and is condensed in silver or platinum vessels at 130°C, looses no formaldehyde perceptible by smell.Often p-cresol dialcohol contains sodium in small amounts as a result of its preparation via its sodium salt. The proportion of sodium is within the range of 0.0 to 5.00/00 (0.000 to 0.037 mole pro mole phenol alcohol).The loss of weight and formaldehyde during the condensation of p-cresol dialcohol in platinum and silver vessels increases with the proportion of sodium.p-cresol dialcohol, free from sodium and hardened in Jena glass (Jenaer Geräteglas 20) and common glass, has a greater loss of weight and a greater loss of formaldehyde corresponding to the capacity of the glass to loose alkali.At 130°C p-cresol dialcohol, free of sodium and hardened in quartz, shows also a weak loss of formaldehyde and a greater loss of weight than in Jena glass. The sodium of the preparation has different effect on the course of the reaction curves.Finally the hardening is accelerated in air in opposition to the condensation in nitrogen the conditions being otherwise the same.
    Notizen: Wird natriumfreier p-Kresoldialkohol in Silber- oder Platingeräten bei 130°C kondensiert, so ist durch den Geruch kein Formaldehyd wahrnehmbar.p-Kresoldialkohol enthält oft von seiner Darstellung über das Natriumsalz her geringe Mengen an Natrium, dessen Anteil im Bereich von 0,0 bis 5,00/00 liegt (0,000 bis 0,037 Mol Natrium je Mol Phenolalkohol).Die bei der Härtung des p-Kresoldialkohols in Platin- oder Silbergeräten beobachteten Gewichtsverluste und die Formaldehydabspaltung sind umso höher, je größer der Natriumgehalt ist.Natriumfreier p-Kresoldialkohol in Gefäßen aus Jenaer Geräteglas 20 und aus gewöhnlichem Glas gehärtet zeigt in Übereinstimmung mit der Abgabefähigkeit an Alkali der letzteren Glassorte neben größerem Gewichtsverlust auch größere Formaldehydabspaltung.In Quarzgefäßen zeigt auch natriumfreier p-Kresoldialkohol bei 130°C schwachen Formaldehydverlust und größere Gewichtsverluste als bei der entsprechenden Kondensation in Geräten aus Jenaer Geräteglas 20.Schließlich zeigen Härtungen unter Luft gegenüber Kondensationen unter Stickstoff bei sonst gleichen Bedingungen einen beschleunigten Verlauf.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 78
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 134-139 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: La composition en acides aminés de la fibroine de soie est examinée par la méthode chromatographique de Stein et Moore. Des fractions de fibroine de soie de différentes solubilités révèlent une différence de teneur en acides aminés.
    Kurzfassung: The amino-acid composition of the silk fibroin is examined with the chromatographic method of Stein and Moore. Silk fibroin fractions of various solubilities reveal differences of amino-acid content.
    Notizen: Das Seidenfibroin wird nach dem chromatographischen Verfahren von Stein und Moore auf Aminosäurezusammensetzung untersucht. Seidenfibroinfraktionen verschiedener Löslichkeit weisen Unterschiede im Aminosäurebestand auf.
    Zusätzliches Material: 1 Ill.
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  • 79
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 178-181 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 80
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 8 (1952), S. 147-155 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Besides chain growth and chain termination also chain transfer has always to be taken into account as a possibility of reaction for the growing chain in radical chain polymerization.However the extent and importance of chain transfer for the polymerization varies greatly with different compounds. The chain transfer constant can be calculated from the dependence of the average degree of polymerization from the concentration of the transfer agent.Some values for the transfer constants of various monomers, initiators and solvents are presented.
    Notizen: Außer der Wachstums- und Abbruchsreaktion muß als Reaktionsmöglichkeit für die wachsende Kette bei der Radikalkettenpolymerisation grundsätzlich immer auch die Kettenübertragung in Betracht gezogen werden. Ihr Ausmaß und damit ihre Bedeutung für den Polymerisationsvorgang ist allerdings von Fall zu Fall sehr verschieden. Aus der Abhängigkeit des mittleren Polymerisationsgrades von der Konzentration des Kettenüberträgers kann die Übertragungskonstante berechnet werden. Es werden quantitative Angaben über die Übertragungskonstanten für einige Monomere, Polymerisationsanreger und Lösungsmittel gemacht.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 81
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 82
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: As the polyxymethylene was used as model of the linear-polymer substances, the products of the reaction between formaldehyd and higher aliphatic diamines can be esteemed as model of total cross-linked polymers.Attemps are described by which is showed, that the white, amorph and unsolulable product of the reaction between hexamethylendiamine and formaldehyd is the total crosslinked polymer of the N,N′-Bismethylenhexamethylendiamine.Dissolving the product with acids, phenol or higher alcohols (in the lasts only at heating to about 160°C), reducing with zinc and hydrochloric acid and reacting with sulforous acid this is degraded to the monomer N,N′-Bismethylenhexamethylendiamine or its derivatives.
    Notizen: Wie das Polyoxymethylen als Modell für linearpolymere Substanzen verwandt wurde, so können die Reaktionsprodukte von Formaldehyd und höheren aliphatischen Diaminen als Modell für völlig vernetzte Polymere angesehen werden.Es werden Untersuchungen beschrieben, durch die gezeigt wird, daß das weiße, amorphe und unlösliche Reaktionsprodukt aus Hexamethylendiamin und Formaldehyd das dreidimensional vernetzte Polymere des N,N′-Bismethylenhexamethylendiamins ist.Beim Lösen des Produktes in Säuren, Phenol oder höheren Alkoholen (in letzteren nur beim Erhitzen auf 160°C), bei der Reduktion mit Zink und Salzsäsure und beim Umsatz mit schwefliger Säre wird dieses zum monomeren N,N′-Bismethylenhexamethylendiamin oder Derivaten desselben abgebaut.
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  • 83
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: En observant le déplacement d'une colonne de liquide dans un tube capillaire à peuprès horizontal, il est possible de déterminer la viscosté en utilisant des gradients de courant extrêmement petits.La vitesse de déplacement de la colonne dépend de I'inclinaison du tube, de la longueur de la colonne liquide, et de la tension de surface au deux bouts de la colonne. L'appareil permet la détermination de viscostés lors de vitesses de courant de I'ordre d'un centiéme de celles obtenues dans des viscosimètres à capillaire verticale. Die plus il est possible de mesurer la variation de la tenion de surface avec le temps. En examinant des solutions de différentes substances macromoléculaires, on constate que I'augmentation de la viscosté, en fonction du gradient s'abaissant vers zéro, s'accentue de plus.
    Kurzfassung: The viscosity at very low gradients of flow can be determined by the movement of a liquid column in a nearly horizontal capillary. The velocity of the column depends on the inclination of the capilary, on the length of the liquid column and on the surface tension at both ends of the column. The apparatus allows to measure viscosities at about hundred times lower gradients than in viscosimeters with vertical capillary. Further the change of the surface tension as a function of time can be measured. Experiments of solutions of various high molecular substances show that the rise of viscosity with decreasing gradients becomes continually steeper toward zero gradient.
    Notizen: Die Bewegung einer Flüssigkeitssäule in einer fast horizontalen Kapillare kann zur Bestimmung der Viskosität bei sehr kleinen Strömungradienten verwendet werden. Die Geschwindigkeit der Säle ist von der Neigung der Kapillare, der Länge der Flüssigkeitssäule und von der Oberflächenspannung an beiden Enden der Säule abhängig. Das Gerät gestattet, die Viskositäten bei etwa 100 mal langsamerer Ströng als im Viskosimeter mit vertikaler Kapillare zu bestimmen. Ferner kann der zeitliche Gang der Oberflächenspannung gemessen werden. An Lösungen verscheindener hochmolekularer. Stoffe wird festgestellt, daß der Viskositätsanstieg mit sinkendem Gradienten gegen den Gradienten Null immer steiler wird.
    Zusätzliches Material: 8 Ill.
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  • 84
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 467-475 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A thorough experimental study of the ionic polymerization of styrene using antimony pentachloride containing radioactive antimony as the catalyst shows that, contrary to earlier work, no catalyst remains attached to the polymer chain. The implication of this finding for the mechanism of ionic polymerization is discussed.
    Zusätzliches Material: 1 Ill.
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  • 85
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 449-456 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The sedimentation equilibrium of polymers in mixed solvents at infinite dilution of polymer was analyzed by thermodynamic methods equivalent to those used by Stockmayer and Kirkwood and Goldberg for the light scattering case. It was found that the apparent weight-average molecular weight in a binary solvent mixture (when nonrefractometric methods are used to measure the experimental concentration gradient) is formally identical with that derived by Lansing and Kraemer on the assumption of stoichiometric combination of one of the solvents with the polymer. The “solvation number” now actually measures a preference for one solvent and can be expressed in terms of thermodynamic quantities characteristic of the ternary polymer-solvent system. In the case of refractometric measurements, where the two solvents have different refractive indices, refraction terms similar to those encountered in light scattering theory for mixed solvents also enter. Under equilibrium conditions, for polymer solutions in pure solvents, thermodynamics can say nothing about “solvation,” which is inseparable from the over-all nonideal behavior at finite concentrations. There is strong reason to believe that all types of experiments designed to measure solvation in mixed solvents under equilibrium conditions must give the same answer, since the same thermodynamic quantities determine polymer-solvent interactions in all cases. By assuming a dynamic equilibrium between sedimentation and diffusion in the equilibrium case and using the sedimentation term for the sedimentation velocity case, an expression for the sedimentation constant in mixed solvents at infinite dilution of polymer has been obtained. This expression is almost the same as that previously derived by Schachman and Lauffer, the difference occurring in an assumption about the density of solvated liquid made by these authors.
    Materialart: Digitale Medien
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  • 86
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 519-527 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polyvinylpyrrolidone (PVP) can be conveniently fractionated from water by successive precipitation with acetone, from chloroform with ether, or from ethanol with benzene. The major part (60-70%) of the common PVP has the intrinsic viscosity of 0.12-0.30. The fractions can be liberated from the low molecular components by extraction of the solid polymer with acetone. Precipitability with ammonium sulfate is a very convenient means of characterizing the fractions. The amount of ammonium sulfate needed to produce turbidity decreases with increasing mean molecular weight of the fractions, with the increasing concentration of the polymer, and with increasing temperature. The molar concentration of ammonium sulfate that produces turbidity is a linear function of the logarithm of the mean molecular weight of the fractions. The amount of ammonium sulfate which produces turbidity decreases linearly with increasing temperature.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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  • 87
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 528-528 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 88
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The rates of initiation Ri of polymer chains in styrene and methyl methacrylate have been measured for four different catalysts. The results for styrene at 60°C are: Ri = 1.28 × 10-5[azo]; Ri = 2.96 × 10-6[Bz2O2]; Ri = 6.12 × 10-7[CHP]; Ri = 9.96 × 10-5[BHP]. Azo, Bz2O2, CHP, and BHP refer to 2-azobisisobutyronitrile, benzoyl peroxide, cumene hydroperoxide, and tert-butyl hydroperoxide, respectively. Rates are expressed in moles per liter per second. The corresponding results for methyl methacrylate at 60° are: Ri = 1.42 × 10-5[azo]; Ri = 6.62 × 10-6[Bz2O2]; Ri = 3.92 × 10-7[CHP]; Ri = 7.30 × 10-8[BHP]. Catalyst efficiencies for azo and Bz2O2 are shown to be nearly unity in both monomers. Chain transfer constants were calculated for all catalysts in both monomers. Photopolymerization was shown to proceed via chains growing in one direction only. The polymerizations were all carried out in the pure monomers (bulk polymerization) with exclusion of oxygen and other inhibitors.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 89
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 573-574 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 90
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 574-576 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 91
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The degradation of polystyrene by heat and ultraviolet radiant energy was followed by mass spectrometric analysis of the gaseous products evolved. Oxygen content, discoloration, and insolubility of the treated polymer were also investigated. The degradation of polystyrene involves two different processes: (1) the breakdown of thermolabile groups formed in the polymer prior to degradative treatment; this breakdown is caused by exposure to heat at 120°C. in vacuo and 115°C. in oxygen and to ultraviolet radiant energy at 120°C. in vacuo and 118°C. in oxygen; it is accompanied by the removal of residual materials such as solvent; and (2) the oxidation of the polymer caused by exposure to ultraviolet radiant energy in the presence of oxygen. The evolution of benzene, methyl ethyl ketone, dimethylbenzenes, and alcohols is associated with the first stage involving the breakdown of thermolabile groups and the removal of residual materials. Compounds such as formaldehyde, formic acid, and acetic acid are produced as a result of oxidation of the polymer. The oxygen content of the polymer was decreased from 0.33 to approximately 0.1 percent by heating at 120°C. in vacuo and at 115°C. in oxygen, and by exposure to ultraviolet radiant energy at 120°C. in vacuo. Ultraviolet treatment at 118°C. in oxygen for 250 hours quadrupled the original oxygen concentration. Discoloration of the polystyrene was definitely noted only on exposure to ultraviolet radiant energy in oxygen and is associated with oxidation of the polymer. The material became insoluble as a result of all heat and ultraviolet treatments. The amount of insoluble material increased with severity of exposure conditions.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 92
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 286-288 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 93
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 309-314 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: To continue the study of the effect of structure on reactivity, an experimental investigation of the free radical copolymerization behavior of eight monomer pairs has been made. The monomer pairs include: vinyl acetate-methyl vinyl ketone; vinyl acetate-1,3-acetoxybutadiene; acrylonitrile-1,3-acetoxybutadiene; methylacrolein-acrylonitrile; vinylsulfonic acid-methyl methacrylate; 2,5-dichlorostyrene-2,5-dimethylstyrene; vinyl acetate-fumaryl chloride; and styrene-fumaryl chloride.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 94
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Intrinsic viscosities of low molecular weight polystyrene fractions measured in an “ideal” solvent (i.e., in cyclohexane at the “θ temperature,” 34°C.) are in accord with the relationship [η]θ = KM1/2. Even at a molecular weight of only 4000, the observed value of K agrees with that for high molecular weights.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 95
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new initiating system, named the “Veroxazine” system, for the copolymerization of butadiene (75)-styrene (25) is described. Ferric versenate is reduced by hydrazine to the ferrous complex which in turn reacts with hydroperoxide to produce the radicals which initiate polymerization. At 5°C., with 5 parts of K-fatty acid soap, 0.1 part of Diox D, 0.1 part of N2H4·H2SO4, 0.0615 part of sodium hydroxide (to give free hydrazine base from the salt), 0.0005 M ferric iron (equivalent to 0.036 part ferric nitrate nonahydrate per 100 parts monomers), 0.0005 M versene, 1 part of K4P2O7 and 0.3 part sulfole, 70% conversion is reached in 12 hours. The rate of conversion can be varied within wide limits by changing the concentration of ferric iron, versene, or hydrazine. Typical conversion-time data at 5°C. with K-fatty acid soap, 0.1 Diox D, and 1 part of K4P2O7 are summarized below. TextFe(III)VN2H4·H2SO4, partConversion, %124812 hrs.0.005M0.002M0.114254790 - 0.002M0.001M0.111224475 - 0.001M0.0008M0.19193264850.0005M0.0005M0.16162848700.0003M0.0002M0.14101938530.001M0.0005M0.417315292 - 0.001M0.0005M0.215274081 - 0.001M0.0005M0.111213362830.001M0.0005M0.05614274766With a given concentration of ferric iron the maximum rate is found with a molar concentration of versene slightly smaller than that of ferric iron. The excess of ferric iron over versene is kept in aqueous solution as the complex with pyrophosphate. The addition of potassium pyrophosphate up to one part increases the rate of conversion and yields a normal latex free from precoagulation. In the absence of pyrophosphate a viscous latex subject to precoagulation is obtained. The effects of kind and amounts of soap, of free acid or base, of kind and concentration of hydroperoxide, kind and concentration of mercaptan, of oxygen, of methanol, and of shortstops have been investigated. Veroxazine recipes which give from 55 to 70% conversion in 12 hours at -5°C. are described.
    Zusätzliches Material: 28 Ill.
    Materialart: Digitale Medien
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  • 96
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 423-432 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: It is evident that a copolymeric mixture, if sufficiently heterogeneous in chemical composition and molecular weight, may separate into two or more distinct phases. The conditions for thermodynamic stability of a single-phase system have been investigated using the modified Flory-Huggins equations for heterogeneous polymer mixtures. The equation for a “spinodal hyper-surface” serves as a sufficient, but not always necessary, condition for phase separation. With certain simplifying assumptions, this reduces to the requirement that two or more phases must exist if: \documentclass{article}\pagestyle{empty}\begin{document}$$ (\bar M_w /\rho )\sum\limits_k {x_k } (\delta _k - \bar \delta )^2 〉 RT/2$$\end{document} where M̄w is the weight average molecular weight, ρ is the density of the high polymer, xk is the mole fraction (or volume fraction) of chains with the same chain-average chemical composition, represented by the “solubility parameter” δk, and δ is the average δ for the whole mixture. For a typical case (M̄w = 100,000, ρ = 1, T = 300°K), the standard deviation in δ cannot exceed 0.055. Since for a typical copolymer the possible range of δ (from 100% of one monomer to 100% of the other) may be 0.5-1.0 δ-units, we conclude that most copolymers must be reasonably homogeneous in chemical composition; the over-all composition of one chain cannot differ greatly from that of another in the same phase.
    Materialart: Digitale Medien
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  • 97
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 453-462 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Using a direct weight method, the rate of butadiene polymer growth has been found to be logarithmic with time and proportional to the initial mass of polymer seed present providing active polymer seeds are used. When solutions of potassium sulfide (0.005 and 0.0025 g. per ml.) were added to butadiene, the growth of popcorn polymer in the vapor phase was greatly inhibited. The final weights of 0.100 g. initial polymer seeds were 0.205 and 0.389 g. after 29.6 and 30.5 days at 60°C. respectively, for the two sulfide concentrations. This is to be compared with a normal growth of 2.85 g. after 13.5 days at 60° for a non-sulfided test. Water does not inhibit popcorn polymer growth and may possibly accelerate it. The activity of the popcorn seeds for spontaneous growth in the presence of monomer depends on the seed generation or extent to which the seeds have grown. The growth activity of a definite mass of polymer increases with continued seed growth until a point is reached where there is a structural change from popcorn-like to more glassy-like polymer. The latter has lower growth activity. It is believed that the effect of variation of activity with seed generation is independent of peroxide content and that these tests were performed with peroxide-free seeds.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 98
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new recipe called the Veroxasulfide Recipe is described for the polymerization of butadiene (75)-styrene (25). The initiating system is composed of ferric versenate, sodium sulfide, and a hydroperoxide. With K-fatty acid soap as emulsifier, the use of 0.00728 part of ferric nitrate nonahydrate (corresponding to 10-4 M ferric iron in the aqueous phase), 10-4 M versene, 0.02 part of sodium sulfide, and 0.1 part of Diox D, the following conversions are found at 5°C.: TextTime, hrs.124812Conversion, %816326685The optimum amount of sodium sulfide is 0.02 part (equivalent to 0.062 part of the nonahydrate) but the rate does not depend critically on the amount. The optimum rate is found with approximately 0.00025 M ferric versenate (8.3% in 8 hours at 5°C.) and the rate may be adjusted conveniently by adjustment of the amount of ferric versenate. The presence of a considerable excess of versene over ferric iron does not affect the rate. With less versene than the amount equimolar to the amount of ferric iron the rate corresponds approximately to that observed with the corresponding amount of ferric versenate; that is, the rate is determined by the amount of ferric versenate rather than by the total amount of ferric iron. Latex of normal fluidity is obtained with charges containing 0.5 part or more of potassium chloride; without added electrolyte thick latex subject to precoagulation is obtained. Satisfactory rates are found with mixtures of Dresinate 214 and K-fatty acid soap. Mercaptan is not needed for initiation; the same rate is found with n-dodecyl mercaptan, with sulfole mercaptan, and without mercaptan. The kind of agitation has no or slight effect on the rate. Added oxygen has only a slight effect which is largely eliminated by the addition of sodium dithionite. A recipe is given which at -5°C. yields 70-75% conversion in 12 hours. Polymerization using the Veroxasulfide recipe at 25°C. may provide a sensitive test for traces of iron in ingredients used in polymerization recipes, since with 2 × 10-6 M ferric versenate (corresponding to 0.1 p.p.m. of ferric iron per liter of aqueous phase), 32% conversion is reached in 11 hours, whereas in the absence of iron 3% conversion is reached in the same time.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
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  • 99
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 9 (1952), S. 478-480 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 100
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Many salts in aqueous alcohol solution can be exchanged for the alkali in oriented filaments of alkali amylose. If the filaments are held taut during exchange, orientation is retained, and excellent fiber patterns are produced. By this method, compounds of amylose were obtained with the iodide, bromide, formate, acetate, and propionate of potassium and with sodium bromide and ammonium fluoride. In addition, potassium bicarbonate-amylose was formed by the action of carbon dioxide on moist filaments of potassium hydroxide-amylose. Data on the composition of the amylose-potassium salt filaments indicate stoichiometric compound formation between amylose and salt, the ratio of salt molecules to glucose residues being 1:2 for the iodide, bromide, formate, and tetragonal form of the acetate, and 1:1 for the propionate and the orthorhombic form of the acetate. As shown by x-ray diffraction patterns, the potassium salts crystallized in two structures. One, based on a tetragonal unit cell, was common to the iodide, bromide, formate, acetate, and bicarbonate; the other, based on an orthorhombic unit, was the stable structure for the acetate and the propionate. Dimensions of the tetragonal unit cells of air-dried filaments of the iodide and bromide were identical, with a0 = 10.7 and c0 (fiber axis) = 16.1 A. Corresponding dimensions for the formate and acetate were 10.8 and 16.1 A., and those for the bicarbonate were 10.8 and 15.8 A. The orthorhombic structures of the potassium acetate and propionate addition compounds with amylose appeared to be isomorphous, unit cells having a0 = 11.0, b0 = 18.1, c0 (fiber axis) = 17.9 A. for the acetate, and a0 = 11.4, b0 = 18.0, c0 = 17.6 A. for the propionate. The tetragonal structural modification is of particular interest. Observed diffraction maxima were consistent with the enantiomorphous space groups, P4121 and P4321, and this, together with composition and density data, demands that the amylose chains posses fourfold screw symmetry, with four glucose residues corresponding to the fiber repeat period of 16.1 A. Succesive residues in the amylose chain must, therefore, be identical. This is the first x-ray evidence which has demonstrated the identity of successive residues in the amylose chain.From a Patterson projection of potassium bromide amylose, the positions of the inorganic ions were determined. The Fourier projection, ρz(x,y), computed from Fhk0 with signs determined by the bromide ion, confirmed the location of the inorganic ions and gave a general outline of the packing of the amylose chains.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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