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  • Polymer and Materials Science  (67)
  • 1945-1949  (67)
  • 1946  (67)
  • 1
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Diethyl silicon dichloride was prepared by a Grignard synthesis and purified highly. The material in various stages of purification was hydrolyzed and then polymerized. The properties of the hydrolyzate and of the final polymer depended markedly upon the degree of purification of the dichloride. The reaction of diethylsilicanediol with phosphorous pentoxide was also studied; the predominating reaction appears to involve entrance of the pentoxide into the polymeric structure, rather than a simple acceleration of the polycondensation reaction by the removal of water.
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  • 2
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 127-145 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This and a following article review the literature from 1910-1945 on polymerization of olefins and diolefins in suspension and emulsion, and present a number of new measurements not published to date. The subject is considered mainly from the point of view of scientific information on the mechanism of polymerization in aqueous suspensions and emulsions, but brief mention is also made of the more important disclosures in the patent literature. The new data presented in this article refer to (1) initial rates of polymerization of styrene, methyl methacrylate, vinyl acetate and acrylonitrile in aqueous suspensions and in soap emulsions as a function of catalyst concentration, temperature, and soap concentration; (2) influence of water-soluble activators, such as sodium bisulfite; (3) influence of initial size of monomer droplets on initial rates of monomer consumption; (4) study, with the aid of the electron microscope, of size of monomer droplets and polymer particles throughout polymerization; and (5) a few experiments on side reactions in the domain of higher conversions. No attempt is made in this paper to review and appraise the very large number of recent patents (from about 1930 on), which protect special procedures on the use of various promoting, regulating, or modifying ingredients. A complete digest of this practice does not exist at present, but reference may be made to the excellent chapter on emulsion polymerization in the book of Talalay and Magat (55), to the very valuable compilation of patents by Hosch in “India Rubber World” (27), and to the enumeration of a selected number of patents in the book of Scheiber (50) on pages 210-213.
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  • 3
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 329-339 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of experiments on the elastic behavior of various textile materials was carried out. All results are described with the aid of a mechanical model. For this purpose it is necessary to introduce the possibility of a blockade of a part of the model. The elastic properties are characterized by the values of seven independent fundamental constants of the model. The value of one of these constants associated with the blockade can be determined experimentally in a direct way; it is found to be independent of the moisture content. The most important properties of the model correspond with the molecular image of Hermans.
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  • 4
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 353-363 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mixtures of butadiene and dimethylbutadiene with varying quantities of styrene and acrylonitrile have been copolymerized under various catalytic conditions at 100°C. The formation of cyclic dimers from dienes and vinyl compounds is, in some cases, much more pronounced than the dimerization of the dienes alone. Since the latter is also a kind of Diels-Alder reaction, a series with increasing dienophilic properties can be established from a comparison of the yields of cyclic dimers. From solubility and swelling experiments it is evident that the polymers prepared from butadiene and the vinyl compounds and those from dimethylbutadiene and acrylonitrile are true copolymers. The mechanical properties of the copolymers from butadiene and increasing amounts of a vinyl compound change gradually from those of a rubber to those of the polyvinyl compound. The copolymers from a mixture containing 30% styrene or acrylonitrile are very similar, respectively, to Buna S and Perbunan. Copolymers of the same composition from dimethylbutadiene and acrylonitrile, on the other hand, form a new class of thermoplastics with a much higher temperature of elasticity.
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  • 5
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 364-379 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The copolymerization in emulsion of butadiene with varying amounts of styrene and acrylonitrile and of dimethylbutadiene with the latter vinyl compound has been studied on a laboratory scale. An essential difference between polymeric vinyl compounds and polydienes is the olefinic character of the latter, which leads to typical secondary changes in the polymers originally formed during the completion of the reaction. Such changes are of fundamental importance for the ultimate mechanical properties of polymers and copolymers based on dienes. After a brief discussion of the general theoretical line of thought serving as a base for our experiments, the influence of various factors on the rate of polymerization is pointed out and demonstrated by experiments. The changes in the nitrogen content of copolymers from acrylonitrile and the yields as a function of the reaction time have also been studied. From an investigation of some physical properties, such as solubility and swelling, the existence of true copolymers (of unknown irregularity) has been established. Copolymers from dimethylbutadiene and acrylonitrile represent a new class of olefinic thermoplastics resembling gutta-percha. Abbreviations used are BP (benzoyl peroxide) and DAB (diazoaminobenzene).
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  • 6
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    Journal of Polymer Science 1 (1946), S. 380-388 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The transversal dimension of the statistical coil formed by a long-chain molecule in solution or in bulk rubber is independent of the longitudinal dimension, h1, of the coil as long as h1 is small compared with the length of the stretched molecule. On the other hand, the lateral dimension of a coil whose longitudinal vector, h1, is oriented in the direction of stretch undergoes a forced contraction during the deformation of bulk rubber. The forced contraction of the transversal dimension is therefore supplying an extra contribution to the entropy change. Its amount has been estimated in earlier work and it influences the numerical factor occurring in the formula connecting the strain-stretch relation for rubber with the molecular weight of the net fragments.
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  • 7
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The course of the reactions of benzoyl peroxide with cyclohexane and cyclohexene may be accounted for by a mechanism involving free radicals and radical chain reactions. With cyclohexane, the average length of the chain hardly exceeds one step and one mole of hydrocarbon reacts with one mole of peroxide. With cyclohexene, chains of two and three steps also occur and about two and one-half moles of hydrocarbon per mole of peroxide take part in the reaction. It is shown that this is due to the one-sided addition of the primary radicals (originating from the peroxide) to the double bond, yielding a new radical without a double bond which can in turn react in the same way with another unsaturated molecule, thus giving rise to polycyclic compounds (chain formation). This polymerization reaction is, however, soon halted by a competitive side reaction involving substitution of the α- (or β)-methylene group, which leaves the double bond intact. In polymerizable vinyl derivatives in which no reactive α-methylene group is present, the competitive reaction cannot occur and the radical chain reaction continues to form a growing chain of interlinked monomeric molecules with annihilation of the double bonds. The two terminal groups of the macromolecules of the final polymerizate are radicals originating from the peroxide used as a catalyst. If a solvent is used, radicals of the latter may also appear occasionally as terminal groups of the polymer. The mechanism of the catalytic action of diacyl peroxides in the polymerization of vinyl derivatives is thus clarified. The molecule linking reaction induced by free radicals in unsaturated compounds also provides an explanation of the action of benzoyl peroxide as a rubber vulcanizer; the peroxide radicals are found as substituents in the rubber molecule.
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  • 8
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 434-436 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By suitable alteration of the exponent the fit of viscosity-concentration data by a Philippoff type equation may be substantially improved. For a series of cellulose acetate solutions the exponent of best fit appears to be related to the physical properties and chemical type of the solvent.
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  • 9
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 10
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 175-182 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The ultraviolet absorption of polystyrene, with maximum absorption at 262 mμ, is due to the presence of phenyl residues in the polymer. The specific extinction coefficient is constant, i.e., independent of the molecular weight of the polymer. This shows that the extinction of the phenyl residues is additive. On the basis of this fact, it is shown that the styrene content of a butadiene-styrene copolymer (such as GR-S rubber) can be determined by ultraviolet spectrophotometry. The relative precision of the determination is about 1%, the probable relative accuracy is about 3%.
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  • 11
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A micromethod is described for density determinations of artificial cellulose fibers by the floating method, in carbon tetrachloride in a dry and air-free atmosphere, permitting an accuracy of one part per thousand. The density is derived from the temperature at which the samples neither sink nor float. This temperature varies, with the kind of fiber, between 45° and 65°C. Measurements of the refractive power were carried out simultaneously. The refractivity calculated according to Gladstone and Dale yields slightly lower figures than those found for model fibers in the preceding communication (Part II). The average difference amounts to seven parts per thousand and is ascribed to a systematic error in the density determinations, due to a slight absorption of carbon tetrachloride by the fibers at elevated temperatures. This explanation is supported by experiments. The density of native ramie, of contracted and reoriented ramie, and of several series of rayon fibers spun with increasing stretch, is given. The conclusion is reached that the density is a measure of the percentage of crystalline substances in the fiber and it is shown that there is a correlation between density and sorptive capacity toward water vapor. The percentage of crystalline matter is estimated to be 55-60% in native ramie and 20-25% in rayon.
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  • 12
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 183-199 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecules of high-molecular substances, for instance, those present in rubber, can be treated statistically in two ways. On the one hand, these molecules are such complicated structures that it is possible to attribute a separate entropy and free energy to each giant molecule. On the other hand, solutions of high-molecular substances represent systems in which the single chain molecule is the elementary particle, and to which statistical considerations and concepts such as entropy and free energy can be applied. Depending upon the parameter considered, the same chain molecule must sometimes be treated as a complicated system and at other times as an elementary particle. The problems originating from the simultaneous existence of two stages in the statistical treatment are examined. It is shown that the entropy of an assembly of many chain molecules is not simply equal to the sum of the entropies of the separate chain molecules. This becomes apparent particularly when determining the distribution function with respect to a particular parameter (e.g., distance between the two end points of a molecule) from a statistical consideration of the single molecule on the one hand, and from a consideration of an assembly of identical molecules on the other hand. The relations between entropy and free energy of the individual particle and the a priori probabilities on which the treatment of an assembly is to be based are explained. It is further shown that the same particle can give rise to a macroscopic phenomenon in two ways and to approximately the same extent: first, as a complicated system, and second, as an element in a large assembly of identical particles. This applies in particular to the elastic retractive force and to the strain birefringence in rubber and related substances.
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  • 13
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of dienes under the influence of heat, of diazoaminobenzene, and of benzoyl peroxide, has been studied. Diazoaminobenzene probably acts as a slow, but continuous, source of free radicals giving quantitative yields of methyl rubber of good quality from dimethylbutadiene after a few days to a few weeks at 100-125°C. The effect of diazoaminobenzene on butadiene is the same, but the rate of the uncatalyzed dimerization of butadiene at 100°C. is as fast as that of dimethylbutadiene at 150°C. and, therefore, dimerization interferes much more strongly with the polymerization of butadiene. Only 60% of polybutadiene has been obtained. A few experiments with isoprene showed its position between the two other dienes. The effect of benzoyl peroxide on the polymerization of the dienes appeared to be much smaller than was expected from its known catalytic action on the polymerization of vinyl compounds, e.g., styrene, for in this case its activity is about 100-1000 times greater than that of diazoaminobenzene. It is assumed that a larger number of radicals, produced by the fast decomposition of benzoyl peroxide, causes this difference. Diazoaminobenzene has about the same effect on the polymerization of styrene and acrylonitrile as on that of the dienes. The catalytic effect of benzoyl peroxide on the polymerization of the dienes is, on the contrary, 10,000-100,000 times smaller than on that of the vinyl compounds. This difference can be understood by the assumption that the catalyst is quickly used up by oxidizing the dienes and their polymers. While methyl rubber and the polyisoprene resemble raw natural rubber, polybutadiene, prepared under comparable conditions, is hard, swells moderately, and has a tendency to become brittle as a result of oxidation (aging). Abbreviations used are DAB (= diazoaminobenzene) and BP (= benzoyl peroxide).
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  • 14
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 217-224 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The chief result of irradiation of cellulose acetate-butyrate with ultraviolet light is cleavage of the cellulose chains so that the average molecular weight is lowered. The exposed material dissolves more slowly in common solvents than the unexposed. The acyl content and carbon and hydrogen contents are not altered appreciably. The rate of the reaction is independent of the type of common mineral impurities, the concentration of expected decomposition products, such as acetic and butyric acids, and the molecular weight of the cellulose ester. Ultraviolet light is necessary for appreciable reaction. Wave lengths shorter than 3500 Å. are most effective; longer wave lenghts are much less active.
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  • 15
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    Journal of Polymer Science 1 (1946), S. 225-228 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A rapid procedure is described for estimating the average molecular weights of polyisobutylenes from deformation-rate measurements.
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  • 16
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    Journal of Polymer Science 1 (1946), S. 229-230 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 17
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    Journal of Polymer Science 1 (1946), S. 230-231 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 18
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 19
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    Journal of Polymer Science 1 (1946), S. 245-246 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A device is described which permits rapid sampling of systems under pressure.
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  • 20
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    Journal of Polymer Science 1 (1946), S. 237-244 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The chain lengths of polymethyl methacrylates prepared with ferrous ion-hydrogen peroxide as the initiating system are consistent with the scheme advanced for the mechanism of the polymerization. The relation between intrinsic viscosity in benzene and molecular weight for fractionated polymethyl methacrylate has been determined and leads to the equation: n = 2.81 × 103 [η]C6H61.32. This equation agrees very well with the data of Schulz, provided that the correct method of extrapolating the osmotic pressures to zero concentration is used. Using the relationship between [η]C6H6 and [η]CHCl3 obtained experimentally, the relation between n and [η]CHCl3 (at 20°C.) is: n = 1.81 l3 × 103[η]CHCl31.22.
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  • 21
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    Journal of Polymer Science 1 (1946), S. 233-236 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that the sedimentation and diffusion constants of cellulose at infinite dilution conform with a formula derived on the assumption of randomly coiled structures. The principle is introduced that the sedimentation velocity of closely packed particles moving through a liquid exerts an influence on their motion, according to known hydrodynamic laws.
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  • 22
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A comparison has been made of the ultraviolet spectrophotometric and chlorine analysis methods for the composition of copolymers of butadiene and p-chlorostyrene. The results of the two methods are in good agreement.
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  • 23
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    Journal of Polymer Science 1 (1946), S. 249-258 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The density-gradient tube is a special glass vessel in which a vertical linear density gradient of almost any desired magnitude can be maintained in a stable condition for prolonged periods by using liquids or solutions of the proper density. This article describes the application of such a device to three typical problems appearing in the field of high polymers: crystallization-rate data, inhomogeneities in composition of copolymers, and rates of polymerization. Possible application to still other problems is indicated.
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  • 24
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The technique of obtaining polystyrene silica replicas from surfaces and cross sections of fibers is described and electron micrographs obtained from replicas of several fibers are shown.
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  • 25
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    Journal of Polymer Science 1 (1946), S. 266-274 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By embedding submicroscopic silver rodlets in micellar systems with fibrous structures, unexpectedly strongly anisotropic rodlet compounds bodies are formed. The observed dichroism, indigo blue-straw yellow, suggests the possibility that a particular anisotropic modification of silver is being dealt with, instead of cubic silver. On applying Wiener's compound body formulas, it appears, however, that in the short-wave region the observed anisotropic effects (negative rodlet double refraction and dichroism) can be computed from the optical properties of isotropic silver. In the spectral region of the average and long waves, differences are found between the observed anisotropy and the value calculated by means of Wiener's formulas. These differences are, however, not of such a nature that it is necessary to assume an unknown allotropic modification of silver with particular optically anisotropic properties in order to explain them.
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  • 26
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    Journal of Polymer Science 1 (1946), S. 289-292 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mixed cellulose acetate-ethers were prepared which contain basic-type nitrogen groups whose films were dyed by xylene brilliant blue. β-Aminoethoxylcellulose acetate was prepared from cellulose diacetate and yarn-type cellulose acetate-propionate using ethyleneimine. β-Cyanoethoxylcellulose acetate was prepared from β-cyanoethoxylcellulose and from cellulose acetate using acrylonitrile with an organic base as catalyst. The solubilities of the mixed ether-esters containing basic type nitrogen groups were less than those of cellulose esters and ethers of comparable degrees of substitution.
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  • 27
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Butadiene and styrene have been copolymerized by the use of sodium sand as a catalyst. The copolymers containing 75 parts of butadiene and 25 parts of styrene and made at 30° and 50° are soluble in benzene and have intrinsic viscosities ranging from 2.5 to 7.5. The copolymers has a very nearly constant composition throughout the course of the polymerization. The amount of butadiene which has entered the chain by 1,2 addition is greater than in the case of the emulsion copolymer.
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  • 28
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Whatever additional factors may be concerned in the production of good vulcanizates from natural rubber by the action of sulfur, there is no doubt that the action of sulfur on olefinic materials in general at the ordinary vulcanization temperature is a chemical one, the primary course of which is determined largely by the constitution of the olefin, and hence may be profitably studied by experimentation with olefins of different unsaturation patterns. Unaccelerated reaction between sulfur and simple monoolefins leads almost exclusively to cross linking of the separate olefin molecules, mostly in pairs, by groups of sulfur atoms. When, however, two or more olefinic units occur in the same molecule, as in the disoprenic hydrocarbons, intramolecular cross linking, i.e., cyclization, at once becomes possible, and the result of sulfur action consists partly in the cross linking of separate molecules as with the monoolefins, but largely in cyclization of the individual olefinic chains, thereby forming sulfur-containing rings. These changes entail a certain loss of unsaturation, from which deductions can be made as to the mechanism of the reaction.
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  • 29
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Experimental data are presented on the monomer composition of copolymers of butadiene and styrene prepared by emulsion polymerization at 50°C. The composition of the copolymers is shown to be unaffected by variations in the amount of emulsifier, of mercaptan, and of the nature of the water-soluble polymerization catalyst. The composition of the copolymers formed from a charge containing 25% styrene (by wt.) can be represented accurately over the entire conversion range by the approximate theory according to which each monomer disappears by a first order reaction with the growing chain of the polymer, without taking into account the fact that the end of the growing chain to which the monomer adds may be a radical derived from either of the two monomer molecules. If the ratio of monomers in the charge is varied within wide limits, however, it is found that the simple theory is not adequate and it is necessary to consider that the chain may end with different radicals. The analysis of the experimental data shows that a butadiene molecule adds more rapidly than a styrene molecule to a radical derived either from a butadience or a styrene molecule.
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  • 30
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Squalene containing six isoprene units is more free of end-group effects and less limited in the range of space-distributional contortions of its carbon chain than mono- and diolefins. Hence it is more comparable with rubber than the latter group where matters of chemical reactivity are concerned. Nevertheless, in its reaction with sulfur, squalene pursues a course very similar to that followed by the diisoprene, dihydromyrcene, in that intramolecular sulfide linkages as well as intermolecular polysulfide linkages are formed. Taking into consideration the amount of sulfur which would suffice for the establishment of some given number of the simplest possible intermolecular linkages (i.e., monosulfide linkages), the efficiency of sulfur as a cross-linking reagent during the vulcanization of squalene is seen to be of a rather low order; this condition might be expected to hold for rubber in the absence of auxiliary mechanisms. So far as can be determined by direct experiment the action of sulfur in forming cross links is not essentially different from that encountered with squalene, since there are indications that both intra- and intermolecular sulfide linkages are formed - the latter being of both dialkenyl and dialkyl sulfide type, and, possibly also of alkenyl alkyl type. Under the influence of small amounts of zinc oxide or of various nitrogen-containing organic accelerators, sulfur reacts with the thiol groups of organic mercaptans forming di- and polysulfides, together with hydrogen sulfide. In the presence of rubber the same reaction occurs without actual liberation of hydrogen sulfide and it thus appears that if any thiol groups are formed as intermediates in vulcanization reactions, they will undergo ready conversion into intermolecular di- and polysulfide linkages. This may well represent an important auxiliary mechanism of cross linking.
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  • 31
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Hydrogen sulfide has often been thought to play an important role in the sulfur vulcanization of natural rubber. A study has therefore been made of the reaction of hydrogen sulfide with olefins, including polyisoprenes, with special reference to the capacity of the reagent to react with olefins in the presence of free sulfur. Comparison of the products so obtained with those derived (a) by light-catalyzed reaction of hydrogen sulfide and (b) by reaction of free sulfur with polyisoprenes has greatly assisted the understanding of the course of sulfur reaction in vulcanization processes.
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  • 32
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the emulsion polymerization of butadiene, styrene, or both, potassium persulfate is often used as the catalyst. A convenient concentration of potassium persulfate in the aqueous layer of the charge is 0.10-0.2%; the method of analysis should therefore be suitable for very small persulfate concentrations. Three methods have been investigated. In the volumetric method the persulfate is allowed to react in an acid medium with an excess of standard ferrous iron, the excess being back-titrated after a given period of time with standard ceric cerium solution. The recommended procedure was found accurate and precise within 0.5%, even at such small concentrations as 5 mg. of potassium persulfate per 100 ml. When latex is analyzed by this method, the polymer is first removed by coagulation with sulfuric acid and the persulfate determined in the filtrate. In order to obtain reliable results the reaction between the persulfate and ferrous iron in the filtrate must be carried out in the absence of oxygen, although this is not necessary in solutions of pure persulfate. The interference by oxygen is attributed to substances of peroxidic character in the fatty acid soaps used as emulsifiers in the emulsion polymerization. The colorimetric method (“Becco” method) is based upon the oxidation of the leuco base of commercial wool green BSMA to a green dye by the persulfate and (colorimetric) measurement of the dye formed. The various factors affecting the accuracy and precision of this method have been investigated and a procedure is given for the analysis of latex. For several reasons, the volumetric and polarographic methods are superior to the colorimetric method. Persulfate in a latex can be determined accurately by polarographic analysis of the latex filtrate after removal of the polymer with sulfuric acid. The polarographic determination can be carried out, in the presence of oxygen, with simple equipment. The method is rapid and precise.
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  • 33
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    Journal of Polymer Science 1 (1946), S. 389-392 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A brief outline is given of the present status of research on the problem of the deformation mechanism of cellulose gels. Emphasis is placed on the prevailing idea of a molecular network structure and recognition of the existence of an intimate relationship between the phenomena of deformation and those of swelling. In these respects the problems involved in cellulose research seem to show a marked convergence with those which emerge from recent developments in rubber research. The principle of Kratky's theory of “affined transformation” and the experiments carried out by this author in order to verify his theory are discussed briefly.
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  • 34
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The paper offers a verification by x-ray experiments of Kratky's theory of affined transformation (affine Raumverzerrung), aiming at an explanation of the mechanism of deformation of swollen cellulose gels upon stretching. Isotropic model filaments of various degrees of swelling were stretched to various extents and x-ray photographs were then taken. Following Kratky, the intensity distribution along the sickles of two paratropic planes of the ribbon-shaped crystallites, the lamellar plane, A0 and the A3 plane (perpendicular to the latter) were measured and the average orientation, expressed in terms of the orientation factor, fx, was calculated. The superposition of the (021) interference on that of the A3 sickle, which had been neglected by Kratky, was accounted for. The experimental results are in conformity with certain characteristic features of the theory; (a) the orientation of the A0 planes advances more rapidly than that of the A3 planes; (b) regardless of the initial degree of swelling of the isotropic filament, the average orientation is actually a univocal function of the elongation, va. On the other hand, the rate of orientation appears to be much greater than that required by theory; the average orientation, expressed in terms of the orientation factor, increases almost twice as rapidly. It is shown, moreover, that, apart from low degrees of orientation, Kratky's theory fails to explain the velocity function of the relative rotation of the crystallites, as derived from the experimental data according to a procedure proposed by Kratky. It is concluded that further work is required to elucidate the mechanism of deformation.
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  • 35
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    Journal of Polymer Science 1 (1946), S. 419-428 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the viscosity of polyvinyl alcohol solutions may be correlated with the chemical nature of the polymer. In particular it is shown that polyvinyl alcohol contains carbonyl groups in the polymer chain, which are to some extent present as ketols. The presence of these keto groups has been demonstrated by a combination of spectrophotometric and chemical techniques. The carbonyl groups appear to be randomly distributed along the polymer chain and also seem to be independent of chain length. The presence of keto groups along the chain allows an explanation for the behavior of aqueous polyvinyl alcohol solutions with acid or alkali.
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  • 36
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A convenient procedure for the determination of polystyrene in GR-S is given. The method depends upon degradation of the GR-S by tert-butyl hydroperoxide in the presence of a trace of osmium tetroxide. Polystyrene is not attacked and is separated by precipitation with ethanol.
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  • 37
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    Journal of Polymer Science 1 (1946), S. 437-439 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 38
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    Journal of Polymer Science 1 (1946), S. 466-474 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of the polymerization of methyl methacrylate in emulsions has been examined. The initial rate of polymerization is independent of the amount of discontinuous monomer phase present and it is concluded that initiation occurs in the aqueous phase. Monomer is observed to disappear from the discontinuous phase more quickly than it polymerizes, and probably forms a monomer-polymer mixture with the polymer produced. An increase in the subsequent rate of polymerization is attributed to the fact that propagation of the growing polymer chains occurs in this monomer-polymer mixture and this entails a decrease in the velocity of termination due to the high viscosity of such mixtures.
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  • 39
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    Journal of Polymer Science 1 (1946), S. 455-465 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An investigation of the copolymerization of many monomer pairs induced by benzoyl peroxide has shown that an order of monomer reactivity with radicals exists. By utilizing the data available, it was possible to make a semiquantitative arrangement of many monomers according to their relative rates of reaction with radicals. A symmetrical selectivity factor is assumed to account for deviations from the order in copolymerization reactions. This selectivity may be attributed to (1) complex formation between monomers or to (2) dipole, steric, or other factors which are independent of concentration. Copolymerization equations have been derived for each case and application of them to styrene-methyl methacrylate mixtures has indicated that selectivity due to (2) is most important in this system. The equation for case (2) has been applied to other copolymer systems.
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  • 40
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    Journal of Polymer Science 1 (1946), S. 529-534 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An elementary theory is given for the rolling of polymeric materials, for the case in which the deformation is largely an irreversible flow of the viscous type. The theory treats the rolling process as the homogeneous deformation of volume elements over the arc of contact and neglects frictional forces that may exist at the roll surface. A numerical example is given of the calculation of roll pressure, which agrees with available data to a factor of two or better. A more complete test will require parallel measurements of viscosity and roll pressure on the same material.
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  • 41
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    Journal of Polymer Science 1 (1946), S. 484-494 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By treating potato juice with acid it was found that potato globulin is converted to albumin and an insoluble casein-like protein. Potato albumin, salted out with ammonium sulfate and purified by dialysis, is very similar to ovalbumin; it is reconverted into a globulin-like protein by alkali. Solutions of potato albumin in water, as well as in acids and alkali, have a very low viscosity. Alkaline solutions of globulin have a greater viscosity than those of albumin; the viscosity numbers of the difficulty soluble protein are even greater. On the basis of the viscosity data, it was concluded that the albumin particles are corpuscular, the globulin molecules are longitudinal, and that the dissymetry is greatest for the difficulty soluble protein particles. On the basis of the different solubilities of all three proteins (which apparently have approximately the same chemical composition), it was concluded that the albumin molecule was the smallest and the difficulty soluble protein molecule the largest. An aqueous solution of potato albumin is denatured when heated to 50-60°, the viscosity thereby increasing more than 100-fold. The solutions become only slightly turbid, but do not flocculate. This unusual viscosity rise can be explained by the transformation of globular albumin molecules into fibrous, elongated particles. Only a slight viscosity increase is observed when alkaline solutions of albumin are heated. Albumin, in the presence of small amounts of salt, is precipitated at 50-60°; the salts also lower the turbidity point. However, very small concentrations of calcium chloride have a stabilizing effect. Albumin is not coagulated at room temperature by 1-2 N salt solutions. The experiments on the effect of cold on potato albumin showed that albumin, after congealing and thawing out, was more easily precipitated than the control solution. The viscosity of the cold-damaged albumin was somewhat less than that of the control solution. It was ascertained that the deaminated product of potato albumin was very similar to deaminated ovalbumin (solutions of high viscosity; linear colloid).
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  • 42
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A general theory is proposed to account quantitatively for the heat polymerization and gelation of the nonconjugated vegetable oils. This is based on a direct approach to polyfunctionality as developed from quantitative considerations of partial random distribution of the fatty acid components in the triglyceride molecules. The differing polymerization rates of linseed and soybean oils are accounted for on the basis of the assumed influence of certain cis-trans geometric isomers. The theory accounts for the anomalous extensive linear polymerization and nongelation of olive oil. Calculations from the theory agree substantially with experimental results on average molecular weight, iodine value, and the percentage of insoluble, infusible cross-linked polymers.
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  • 43
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    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
    Notes: Equations are derived for stress-strain curves for a hypothetical model substance containing a large number of like systems, each assumed to be in equilibrium between two states having different arrangements of the atoms. With this model one can study the dependence of the initial elastic modulus, the limiting strain (for infinite stress), and the over-all shape of the stress-strain curve on characteristics of the rearranging systems - their number, the initial energy difference between the two states, the shift of atomic positions, etc. Introduction of an assumed proportionality between the shift per rearrangement and the square of the relative length of the sample (in the direction of the shift) leads to stress-strain curves similar to those determined experimentally for natural rubber and other rubberlike materials.
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  • 44
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    Journal of Polymer Science 1 (1946), S. 22-36 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Reduced chicken feather keratin forms a soluble complex in neutral aqueous sodium alkylbenzenesulfonate (average: dodecylbenzenesulfonate). The chemical composition, specific refractive increment, partial specific volume, electrophoretic mobility, osmotic pressure, diffusion constants, and ultracentrifugal sedimentation of the complex have been studied. The complex is heterogeneous but similar to egg albumin-sodium alkylbenzenesulfonate mixtures previously studied in general properties, including fiber-forming properties, the average molecular weight of the dispersed protein units, and the relative symmetry of the dispersed units in dilute solution.
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  • 45
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Previous observations make it probable that one or both ends of a longchain molecule produced by catalyzed vinyl polymerization contain fragments of the initiator. If one uses acid peroxides as initiators, these fragments can contain a carbonyl group. It is the purpose of this paper to investigate whether these carbonyl groups which are present only in a very small amount can be detected by infrared absorption. It seems that in the case of polystyrene initiated with benzoyl peroxide, infrared absorption spectra reveal the presence of a small amount of some carbonyl groups in the polymer. Their amount appears to be in agreement with chemical measurements and with the molecular weight of the material.
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  • 46
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    Journal of Polymer Science 1 (1946), S. 37-43 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Using the copolymer composition equation, the critical constants α and β are determined for the systems styrene-2,5-dichlorostyrene, styrene-methyl acrylate, styrene-diethyl maleate, and styrene-diethyl chloromaleate.
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  • 47
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    Journal of Polymer Science 1 (1946), S. 44-48 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Results are reported of experiments designed to delineate more clearly the action of retarders and chain transfer agents and to place different labeled end groups at either end of polystyrene molecules.
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  • 48
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    Journal of Polymer Science 1 (1946), S. 49-57 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 49
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    Journal of Polymer Science 1 (1946), S. 58-62 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Further experimental evidence is given which indicates that, when a dilute solution of GR-S is mixed with carbon black, certain fractions of the rubber are preferentially adsorbed by the black. After removal of the carbon black and the adsorbed fractions by centrifuging, the “treated” GR-S is obtained by precipitation from the solution. Samples compounded as GR-S gum stock show increasing modulus with increasing amounts of carbon black used for adsorption treatment. However, when the GR-S thus treated is compounded with carbon black, then the effect is reversed. The more black used in the treatment and the higher the modulus of the gum stock, the lower the modulus of loaded stock.
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  • 50
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
    Notes: The dimensional stability of molded thermoplastic articles is a function of the extent to which stresses are frozen into them on molding. The kind and amount of plasticizer included in the material to be molded may be varied to minimize the amount of these stresses. Methods of obtaining fundamental information about polymer-plasticizer systems from simple measurements of viscosity and osmotic pressure are suggested in this paper, and some results for cellulose derivatives are given.
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  • 51
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    Journal of Polymer Science 1 (1946), S. 75-82 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Flory-Wall expressions for the fraction of substituents remaining on a vinyl copolymer, when substituents are removed at random from adjacent 1,3 positions, are extended to the case of nonrandom copolymerization. A copolymer composition equation is derived for the case in which the type of monomer preceding the active freeradical chain end affects the propagation reaction. The distribution of lengths of sequences in copolymers is discussed.
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  • 52
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence on polymerization and copolymerization of various structural factors, especially polarity at the double bond of the monomer, is discussed. The effect of substituents in donating or withdrawing electrons appears to be an important regulating factor in copolymerization.
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  • 53
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    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
    Notes: The interaction of polymers and liquids can be fairly well characterized by the value of the quantity μ, commonly used in thermodynamics of polymer solutions and usually evaluated from osmotic pressure measurements. The Flory-Rehner theory of swelling relates the amount of swelling of a slightly cross-linked polymer in a liquid to μ and a parameter Mc, the average molecular weight between cross links. Mc, may be determined for a cross-linked polymer from its swelling volume in a solvent in which osmotic pressure measurements with the noncross-linked polymer have given the value of μ. The cross-linked polymer, thus calibrated, can be used to obtain the μ value for other liquids by measuring its swelling volume in them. This procedure has been carried out on polyvinyl chloride which can be cross linked by heating. Calibration in three different liquids gave comparable values of Mc, thus checking the Flory-Rehner theory. The quantity μ was determined at two different temperatures for fifty liquids. The value of μ and its temperature dependence correlate well with the observed properties of the binary systems. Variation of μ with molecular weight in an homologous series is demonstrated.
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  • 54
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    Journal of Polymer Science 1 (1946), S. 121-126 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Nitrogen was introduced into cellulose acetate by the incorporation of amino acid groups. Some of the mixed esters were soluble in organic solvents. Cast films were examined for dyeing properties with wool-type dyes. Many of the mixed esters containing above 1% nitrogen dyed well with xylene brilliant blue, a typical wool-type dye, Mixed cellulose acetate esters were synthesized containing glycine, dl-α-alanine, β-alanine, and α-isoaminobutyric, d-glutamic, and p-aminobenzoic acids. The amino groups were protected by acetylation prior to use. The N-acetyl amino acids were treated with cellulose diacetate in dioxane solution containing chloroacetic anhydride and magnesium perchlorate as impellor and catalyst, respectively. Cellulose acetate metanilate was prepared by use of the aminosulfo acid chloride. An attempt was made to prepare 6-aminocellulose by the reaction of aqueous ammonia, and also sodamide in liquid ammonia on 6-iodotosylcellulose acetate. Only traces of nitrogen were introduced by this procedure and the recovered products showed signs of extreme degradation.
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  • 55
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    Journal of Polymer Science 1 (1946), S. 146-146 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
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  • 56
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    Journal of Polymer Science 1 (1946), S. 147-147 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
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  • 57
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    Keywords: Chemistry ; Polymer and Materials Science
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    Notes: In this paper it is emphasized that density is a typically macroscopic concept which cannot be transferred to small particles or bodies with small pores. This fact has not been duly accounted for in earlier work on the density of cellulose fibers. The usual interpretation of density determinations in various media is criticized and the point of view that cellulose fibers should be considered as porous bodies is dropped. The pore system occurring in native fibers is coarse enough not to interfere with density determinations in indifferent organic liquids.It is shown experimentally that even substances like water and glycerol penetrate very slowly into dry cellulose and that indifferent organic liquids do not penetrate at all. In the experiments with water vapor a new phenomenon, the heterogeneous course of absorption, is observed, giving rise to sharp microscopically visible boundary lines between the wet and the dry portion of the fiber.
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  • 58
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    Journal of Polymer Science 1 (1946), S. 156-161 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Accurate determinations of the density and refractive power of various types of model filaments prepared from viscose in the bone-dry state were made. The molecular refraction, according to the formula of Gladstone and Dale, was calculated and shown to correspond within three parts per thousand with the refraction calculated from atomic refractions. It is concluded that the liquid used for the density determinations (mixtures of carbon tetrachloride and nitrobenzene) does not penetrate into the fiber substance. The technique of the experiments is described in detail. The immersion liquids used in the optical measurements were standardized mixtures of butyl stearate and tricresyl phosphate; contamination with moisture during the measurements was definitely excluded.
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  • 59
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    Journal of Polymer Science 1 (1946), S. 172-174 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
    Notes: In the following paper the crystallization of submicroscopic cellular strands from multimolecular, cellulose films is illustrated by electron micrographs.
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  • 60
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    Journal of Polymer Science 1 (1946), S. 441-444 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new method for the determination of the activation energy for the setting of silicic acid solutions is described. Experimental results point to the conclusion that setting to a gel occurs at a definite stoichiometric point which is independent of temperature.
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  • 61
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    Notes: In using the velocity ultracentrifuge in conjunction with free diffusion measurements for the determination of molecular weights of polymolecular systems, it is desirable to know what average molecular weights are obtainable. These average values are not simple moments of the molecular weight frequency curve, but depend on the methods of experimental observation, and on the hydrodynamic character of the molecules in solution. Most often, however, the average molecular weight falls between the number and weight-average values.
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  • 62
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    Journal of Polymer Science 1 (1946), S. 475-483 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relationships which exist between the solvation and shape of colloid particles, as well as between solvation and viscosity, are discussed. From the most important experiments on these subjects the following conclusions may be drawn. Solvation is dependent on the size and shape of the particles and on the chemical relationship of the dispersion medium to the dispersed portion. True or chemical solvation is generally very small and there is no reason to speak of a thick and tightly bound solvent layer. The solvation of compactly formed particles of spherocolloids is greater, the smaller the particles (all other conditions being equal). Solvation is greater, the more loosely the particles are formed (for dispersion mediums having similar chemical properties and for similar dispersed or dissolved substances). Solvation increases when a corpuscular particle is transformed into a rodlike or threadlike particle; the viscosity also increases; if the threads are further broken down into smaller fragments, then the viscosity decreases, but a further increase in the chemical solvationis supposed to occur. The stability of many lyophilic sols, especially the proteins, depends very little on the solvation; it is mainly dependent on the chemical characteristics of the atomic groups which are found on the surfaces of the particles; the least stability is found for surfaces which contain heteropolar groups - that is, surfaces which have the same number of positive and negative ions.
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    Journal of Polymer Science 1 (1946), S. 535-539 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the rolling of Plastic sheet the viscous work gives rise to heating of the plastic sheet. The maximum temperature reached in the interior of the sheet during shearing is of the interest, both in the theoretical calculation of roll pressure, and from the point of view of possible thermal decomposition effects. A calculation is given for a simple, some-what artificial, model, which leads to an upper value for this maximum temperature if a measurement of the average temperature of the emergent sheet is given. The model taken is that of an infinite sheet, of thickness 2δ, in which heat is continuously liberated at the rate of 4ηφ2 cal. cc. -1 sec. -1, where φ is the relevant value of the rate of compression (assumed constant across the sheet). The curve giving the temperature distribution across the sheet is calculated numerically for two cases; it is relatively flat, as would be expected on physical grounds, since the viscosity, η, decreases as the temperature rises. It is concluded that these thermal effects may be neglected in the calculation of roll pressure in Part 1.
    Additional Material: 3 Ill.
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  • 64
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 540-548 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyvinyl alcohol may be reacted with methoxyacetaldehyde, 2-methoxyethoxyacetaldehyde, 2-methoxyethoxyacetaldehyde, 2-n-propoxyethoxyacetaldehyde, tetrahydrofurfuryloxyacetaldehyde, or 3-methoxypropionaldehyde, or with mixtures of these aldehydes, to yield thermoplastic resins which are soluble in cold water below specific temperatures peculiar to each resin, and which are soluble in most organic solvents except aliphatic hydrocarbons.
    Additional Material: 2 Ill.
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  • 65
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 549-580 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This and a previous article (p. 127) review the literature from 1910-1945 on polymerization of olefins and diolefins in suspension and emulsion, and present a number of new measurements not published to date. The subject is considered mainly from the point of view of scientific information on the mechanism of polymerization in aqueous suspensions and emulsions, but brief mention is also made of the more important disclosures in the patent literature. The new data presented in this article refer to (1) initial rates of polymerization of styrene, methyl methacrylate, vinyl acelate and acrylonitrile in aqueous suspensions and in soap emulsions as a function of catalyst concentration, temperature, and soap concentration; (2) influence of water-soluble activators, such as sodium bisulfite; (3) influence of initial size of monomer droplets on initial rates of monomer consumption; (4) study, with the aid of the electron microscope, of size of monomer droplets and polymer particles throughout polymerization; and (5) a few experiments on side reactions in the domain of higher conversions. No attempt is made in this paper to review and appraise the very large number of recent patents (from about 1930 on), which protect special procedures on the use of various promoting, regulating, or modifying ingredients. A complete digest of this practice does not exist at present, but reference may be made to the excellent chapter on emulsion polymerization in the book of Talalay and Magat, to the very valuable compilation of patents by Hoseh, and to the enumeration of a selected number of patents in the book of Scheiber.1
    Additional Material: 12 Ill.
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  • 66
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 1 (1946), S. 581-581 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 67
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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