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  • Polymer and Materials Science  (150)
  • ASTROPHYSICS
  • PROPULSION SYSTEMS
  • 1970-1974
  • 1965-1969  (170)
  • 1960-1964
  • 1965  (170)
Collection
Publisher
Years
  • 1970-1974
  • 1965-1969  (170)
  • 1960-1964
Year
  • 1
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A study has been conducted of the kinetics of the reactions of primary and secondary alcohols with phenyl isocyanate in the presence of metal catalysts. It has been determined that the type and concentration of metal catalyst, the structure of the alcohols, and the type of solvent play an important role in the reaction rates and ratios of rate constants. Catalysis by lead naphthenate increased the reaction rates of 2-methoxy-l-propanol and 1-methoxy-2-propanol more than 3-methoxy-1-propanol, whereas catalysis by dibutyltin dilaurate enhanced the reaction rates of 3-methoxy-1-propanol more than those of 2-methoxy-1-propanol and of 1-methoxy-2-propanol. Dibutyltin dilaurate has been found to impart a high ratio of Kprimary/Ksecondary, where the primary alcohol was 3-methoxy-1-propanol and the secondary alcohol was 1-methoxy-2-propanol. Determinations of mixtures in toluene solutions containing up to 75%, of 3-methoxy-1-propanol were made with good accuracy.
    Additional Material: 1 Ill.
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  • 2
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Aromatic diamines react with pyromellitic dianhydride in solvents such as dimethyl-acetamide to form solutions of high molecular weight polyamic acids. These soluble polymers can be converted to insoluble aromatic polyimides. The aromatic polyimides exhibit zero strength temperatures above 700°C. and possess excellent thermal and oxidative stability. The stability characteristics of films and the relation of chemical structure to thermal and hydrolytic stability and to polymer properties such as crystallinity are described.
    Additional Material: 14 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 1911-1939 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By use of a modified, small-bore, capillary extrusion rheometer (MCER) with an Instron tensile testing machine, the flow and set-up properties of thermosetting plastics and rubbers were characterized. The majority of the experiments were performed with diallyl phthalate, where the rate of curing was also followed by infrared determination of the reduction in unsaturation as the polymerization-curing proceeded. Phenol-formaldehyde was also characterized. Finally, the curing of ethylene-propylene and ethylene-vinyl acetate copolymer rubbers with peroxide was studied and correlated with the type of peroxide used. The MCER data are shown to be of practical use for predicting the time-temperature-pressure relationships for processing thermosetting plastics and rubbers. Moreover, the history of the curing, as obtained by analysis of the continuously extruded strand, is also of theoretical interest for studying reaction kinetics and for evaluating the effectiveness of various curing systems. It is predicted the MCER will be widely used for studying the curing of thermosetting plastics and rubbers.
    Additional Material: 30 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 1941-1948 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The concentration dependence of the reduced viscosity has been studied for several polyelectrolytes in conductivity water. It is shown that the viscosity maximum previously reported for polyelectrolyte solutions without added electrolyte can be explained either by the presence of ionic impurities in the solvent or by the contamination of the solutions. It is concluded that the folding chain theory of polyelectrolyte solutions requires amendment to account for the experimental results on counterion association. A suggested amendment to the theory implies that the application of the Huggins equation to the concentration dependence of polyelectrolyte solutions in the presence of added electrolyte may not lead to information concerning the interactions between the polyions in solution.
    Additional Material: 1 Ill.
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  • 5
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The acrylic esters of carnuba wax alcohols and the vinyl esters of nonhydroxy carnuba wax acids have been synthesized. The acrylic and vinyl esters have been homopolymerized and copolymerized with vinyl chloride. Acrylonitrile-acrylic ester copolymers also have been prepared. The copolymers were quite brittle when molding was attempted.
    Additional Material: 4 Tab.
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  • 6
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Homopolymers and copolymers with vinyl acetate and vinyl chloride have been prepared from the vinyl esters of 9-chlorostearic acid, 12-chlorostearic acid, 14-chloroeicosanoic acid, 9-hydroxystearic acid, 9,10-dihydroxystearic acid, 14-hydroxyeicosanoic acid, and 8-(1,3-dioxylone-2-yl) octanoic acid.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 4001-4011 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The investigation of the crystal and molecular structure of optically active poly-D(-)-β-methyl-ε-caproamide was carried out in two stages. The molecular conformation was first studied by means of Fourier transform methods and the crystal packing was later deduced by detailed structure factor calculations. The structure thus established bears some close resemblance to that characteristic of the γ modification of unsubstituted nylon 6. A marked shortening of the chain along its axis is produced by the presence of a methyl group in the β position. This causes the rotation about the skeleton bonds adjacent to the amide bonds, whereas the rest of the chain retains its trans planar stable conformation. The hydrogen bonds of normal length (2.85 A.) crosslink the molecules in parallel sheets in planes parallel to the (100) plane which are translated with respect to each other by 5/14 of the b axis in the P21 monoclinic space group.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 3 (1965), S. 497-508 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ability of periodate-oxidized amylose to form aggregates in aqueous solution was studied by sedimentation, light scattering, and viscosity analyses. Ultracentrifuge schlieren patterns show that aggregation can be appreciable at pH 3.0 and 1.0. The hydroxyl ion-catalyzed degradation of the oxidized amylose is faster at pH 3.0 than at pH 1.0. Viscosity and sedimentation analyses conducted at pH 3.0 show that a minimum in the degree of aggregation of the oxidized molecules is obtained at 15-25% oxidation. Solubulity studies and x-ray diffraction patterns on retrograded amylose show that maximum solubility of the retrograded amylose is obtained by oxidizing to the extent of 25-35%. It was therefore concluded that in the general range of 20-30% periodate oxidation, the oxidized amylose has a minimum ability to form intermolecular hydrogen bonds. Outside of this range, oxidized amylose readily forms aggregates in aqueous solutions.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 3 (1965), S. 491-496 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Calorimetric measurements of the heat of the addition of the second strand of poly U to poly (A + 2U) to form the three-stranded poly (A + 2U) complex in 0.1M and 0.5M NaCl at 24 and 37°C. are reported. A value of ΔH = -3800 cal./mole of poly (A + 2U) formed was found to be fairly insensitive to the experimental conditions employed. The heat of the addition of the third strand to the preformed poly (A + U) helix is considerably less exothermic than the heat of reaction between poly A and poly U to form poly (A + U). The insensitivity of the heat of addition of the third strand (poly U) to changes in salt concentration and temperature lends qualitative support to the earlier hypothesis that the major portion of the variation of the ΔH of the poly A and poly U reaction with experimental conditions arises from differences in the conformation of poly A. Combining the information obtained in this study for the ΔH of the reaction forming poly (A + 2U) with data for the ΔH of the formation of poly (A + U) indicates that the conversion of poly (A + U) to poly (A + 2U) is opposed by an enthalpy change which increases with temperature. Extrapolation of these values to 52°C. where poly (A + U) is transformed to poly (A + 2U) in 0.5M NaCl leads to a value of ΔH = +3800 cal./mole (A + 2U) formed and ΔS = 11.5 cal./mole of (A + 2U) formed. It is concluded from the calorimetric data that the driving force for the poly (A + U) to poly (A + 2U) conversion reaction is the favorable entropy change.
    Additional Material: 1 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 3 (1965), S. 461-480 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of salt type and concentration on the transformation of an oriented crystalline collagen tendon into a crosslinked network under conditions of equilibrium swelling was investigated. Our main observations are the following. The degree of swelling of crystalline tendons increases at low salt concentration Cs, and decreases at higher Cs for a wide variety of salts. The observation is not reconcilable with swelling taking place in interfibrillar spaces or structural voids. Within the tropocollagen units and at their ends, regions of reduced organization are postulated (as suggested by Bear and by Schmitt) which are able to interact with the diluent in the amorphous-like manner. At least four different factors should be considered in assessing the role of salt and salt concentration on the shrinkage temperature Ts under isoelectric conditions. They are: (1) specific effects, (2) diluent effects, (3) crosslinking effects, and (4) nonequilibrium effects. The diluent effects are correlated with the salting-in-salting-out power of the ions which was characterized in Part I of this series. Smaller amounts of diluents are generally available to the tendon when the salt has a higher salting-out power, and this corresponds to higher shrinkage temperatures, other conditions being the same. The crosslinking effect raises Ts due to a reduction of the diluent content and, probably for p-benzoquinone and formaldehyde, also to a reduction of the conformational entropy in the molten state. Nonequilibrium effects arise from the fact that shrinkage and recrystallization are kinetically hindered when the tendon is highly deswollen in strong salting-out solutions, or when the salt has a crosslinking power. The specific effect is the only effect which is not related to the amount of diluent present in the tendon. Its origin is less clear. For anions such as Cl- and SCN-, it is possibly related to an ability of the ion to prevent intersegmental hydrogen bonding and water carbonyl bridges. The competition of several of the above effects for a given salt solution makes possible various types of dependence of Ts upon Cs: Ts may either continuously decrease or continuously increase with increasing Cs, or it may go through a minimum. In absence of salt, the cooperative character of the transition at the pH at which maximum swelling occurs appears extremely reduced. The large swelling maintains the tendon in the elongated state and this simulates a continuous decrease of Ts on lowering pH. In presence of small quantities of salt, which reduce swelling, the transition is sharp and Ts is decreased with pH up to pH 2, when maximum swelling occurs, and then reincreases on further lowering of the pH. The dependence of Ts upon Cs is more complex than under isoelectric conditions. There is generally an increase of Ts with Cs which is equivalent to an increase of the denaturation temperature with Cs for helical polyelectrolytes in solution. At higher salt concentrations, however, Ts may decrease again, and possibly increase again at still higher salt concentrations, depending upon the effect of the salt solution in the isoelectric zone.
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