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  • 1
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The hydrodynamic properties of native and urea-denatured fibrinogen have been investigated, primarily to examine further the suggestion, based on a consideration of data for horse serum albumin, that urea denaturation may involve swelling instead of increased asymmetry. A sedimentation-diffusion and also a light scattering molecular weight determination at the isoelectric point indicate that 6 M urea causes neither splitting nor aggregation of the native protein in the denaturation process. The observed increase in the intrinsic viscosity and frictional coefficient upon denaturation can be interpreted in terms of an equivalent hydrodynamic ellipsoid of approximately the same shape but of a volume which is approximately 1.7 times that for the native protein. The effective volume appears to be slightly dependent on pH with a minimum at the isoelectric point. It thus appears that the urea denaturation of bovine fibrinogen, like that of horse serum albumin, may involve swelling. There is no indication in the case of either protein that increased asymmetry is involved in accounting for the frictional behavior of the denatured substances.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 43 (1960), S. 579-579 
    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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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cobalt complex compounds exhibited varying degrees of activation and retardation in butadiene-styrene-soap emulsion polymerization systems at 20-50°C. An accompanying effect was the wasting of modifier, particularly by large concentrations of activator. The most active complexes for use with dodecyl mercaptan were those in which the cobalt was coordinated with two or more negative groups other than thiocyanate, and in which the neutral coordinated groups were not ethylenediamine.
    Additional Material: 17 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 2125-2131 
    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: p-Phenylene oxadiazole/N-methyl hydrazide copolymers were prepared by polymerization of terephthalic acid, dimethyl terephthalate, and hydrazine sulfate in fuming sulfuric acid, and coagulation of the polymer was obtained in aqueous sulfuric acid. Fibers spun from these copolymers have unusually high strength and modulus, making these materials attractive for the reinforcement of articles such as tires. Yarn tenacities of 16-21 gpd and moduli of 350-450 gpd were obtained. Yarn of these copolymers showed no significant degradation under conditions to which a tire cord material is subjected in tire building and end use. In their performance in vehicle tires, tire cords were found to be competitive with other reinforcing agents such as fiber glass, steel, and commercial poly(p-phenyleneterephthalamide).
    Additional Material: 6 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 2189-2195 
    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 polyhydrazide was prepared from terephthaldihydrazide (TDH) and terephthaloyl chloride (TCl) and copolyhydrazides from oxalicdihydrazide (ODH) and from TCl with a 50:50 molar mixture of ODH and TDH. The 50:50 copolymer gave superior spinning performance and fiber properties and was studied extensively as a candidate for tire cords. The best yarn tensile properties were 21.6 gpd (grams/denier) tenacity, 6% elongation, and 443 gpd modulus. Temperature resistance and creep resistance were good, while the resistance to uv light was only fair. Stability in rubber and adhesion to rubber were good. In radial tires built with equal-strength belts, mileage from tires having the copolymer cord in the belts was equal to that of steel-belted tires.
    Additional Material: 4 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 1387-1401 
    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: The characteristics of Monvelle, a new biconstituent fiber from nylon 6 and a segmented polyurethane, are reviewed briefly, and some of the technical problems inherent in producing such a fiber are discussed. The characterization of two series of polyurethanes which can be melt spun is given in detail. The chemical composition of the hard segment was maintained constant, being derived from 4,4′-diphenylmethane diisocyanate (MDI) and 1,4-butanediol, in all polymers. In one series using poly(butylene adipate) of MW 2000 as the soft segment, the average hard segment content was varied from 33% to 54%. In the other series, the hard segment content was held at 43%, and three additional soft segments, each at MW 2000, were used: poly(ethylene adipate), polycaprolactone and poly-1,4-oxybutylene glycol (PBG). Characterizations include molecular weight distributions, thermal analysis, rheological studies, and selected small-angle and wide-angle x-ray diffraction and polarized light microscopy. Crystallinity, melt viscosity, and activation energy of flow increased with increasing hardsegment content. Changes in the polyester soft segments had little effect on the properties studied, but with PBG the crystalline melting point of the polymer, without annealing, was higher and the melt viscosity was slightly higher than corresponding polyester-based samples, in agreement with previous reports of sharper phase separation in polyether urethanes, compared to polyester urethanes.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 27 (1988), S. 1897-1904 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The secondary structure of the human growth hormone releasing factor (GRF 1-29) in a solution mixture of 60% aqueous phosphate buffer:40% 2,2,2-trifluoroethanol-d3 has been investigated by two-dimensional 1H-nmr spectroscopy. Sequential resonance assignments and elements of secondary structure were obtained from phase-sensitive correlation spectroscopy, relayed coherence spectroscopy, and nuclear Overhauser spectroscopy experiments. The observation of a large number of α-amide and amide-amide interresidual nuclear Overhauser effect connectivities as well as the existence of 11 slowly exchanging amide protons indicates that the peptide adopts a well-defined secondary structure most likely constituted of a single long helix. This conclusion is consistent with the CD measurements.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 1053-1074 
    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 series of model polyurethanes and polyureas, a polyamide, and a polyimide were prepared by reacting 4,4′-diphenylmethane diisocyanate or polyisocyanates having similar polybenzyl structures with aliphatic or aromatic coreactants. Thermogravimetric analyses indicated that the flammability of the polymers was related to the formation of volatile flammable products during early stages of decomposition. Determinations of the heat evolved during differential thermal analyses and of the thermodynamic heats of combustion suggested that the extent and rate of reaction were among the important factors governing flame propagation. Flame-resistant polymers were prepared by use of structural elements which were thermally stable and nonvolatile or which formed nonflammable decomposition products.
    Additional Material: 12 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 1277-1288 
    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: The development of new and more sensitive techniques in thermal analyses aids in a more complete understanding of the contributions of individual components in urethane elastomers regarding their mechanical and thermodynamic behavior. The behavior of various segments of the elastomers reported in this work illustrates a clearer interpretation of reasons for changes in mechanical behavior caused by changes in heat capacity, volume and tensile properties; the gross changes previously reported for polyurethane properties as a function of temperature are also confirmed with a more exact definition of their origin.The sub-ambient temperature behavior and response of physical measurements near the melting point of the backbone polyol are largely a function of the so-called “soft block.” The soft block does not contribute to the mechanical properties above the melting point of the polyol unless some urethane segments from the diisocyanate and extender are structured into the soft block, that is, excess diisocyanate and extender are added to build in the “hard” block. The extender and isocyanate influence for both low and high temperature properties is observed by the lack of molecular fit imparted to the backbone polyol as well as some crystallinity in the polymer hard block. The usual Tg transition reported in urethane elastomers corresponds to a first-order transition in the polyester or polyether backbone.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 30 (1958), S. 479-492 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt has been made to combine the advantages of the rapid, base-catalyzed addition polymerization of caprolactam with the more stable molecular weight distribution given by the much slower polycondensation process. This aim has been achieved by polymerizing the monomer in the presence of sodium hydroxide or carbonate and, at a later stage, introducing a small amount of a second agent which promotes hydrolysis or segment interchange reactions and which thus accelerates the chain length re-distribution of the polymer. The polymerization and molecular weight re-equilibration steps can be conveniently conducted as two distinct, consecutive batch processes or can be operated on a continuous basis. The practical, industrial significance of these results is discussed. Suitable agents promoting the re-distribution reactions include water, 6.6 nylon salt, aminocaproic acid, acetic acid, and n-butyl alcohol. All experiments were carried out at 250°C. under a nitrogen atmosphere and the course of the reaction was followed by measurement of the rate of change of the water-soluble content of the polymer, and of its end group concentrations, solution viscosity and, in part, turbidity titrations of the water-extracted products. An observation incidental to the main aim of this work was that the polycaproamide, after washing with water, contained an excess of free amine end groups over carboxyl terminal units. No chain branching was detectable from solution viscosity or infrared spectral investigations, and the polymer was free from sodium. Similar end group effects have been previously described by Dutch and German workers.
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