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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 15 (1994), S. 445-445 
    ISSN: 1022-1336
    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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  • 2
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 14 (1993), S. 785-790 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 3
    ISSN: 0935-9648
    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
    Additional Material: 2 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 1141-1149 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An electron spin resonance (ESR) study has been made of radicals trapped in polyisobutylene irradiated at 77 K. It is concluded that only the —C(Me)2—CH— radical remains after heat treatment above 213 K. This radical shows a very sharp doublet ESR spectrum with hyperfine splitting of about 2.2 mT. A broad doublet ESR spectrum observed without warming, which was previously assigned as —C(Me)2—CH—is explained as a mixture of a doublet and a triplet due to the —C(Me)2—CH— and radicals. γ-irradiation at 77 K produces these major radical components and other carbon radicals as minor species. It has also been found that a conversion of other radicals into —C(Me)2—CH—occurs without decay on annealing below 183 K. Heating in the range 183-213 K causes both conversion and decay of the radicals. On annealing above 213 K, only decay occurs. The ESR spectra of polyisobutylene radicals are easily saturated by microwave power even at 1.6 μW. The mechanism of radiolysis for polyisobutylene is briefly discussed.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 2883-2895 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kerateine gel, prepared by reducing wool keratin with alkaline 2-mercaptoethanol-urea solution and by partially reoxidizing the dissolved kerateine, reduced iron(III) to iron(II). Reduction of iron(III) was enhanced by addition of copper(II). Reduction of methylene blue (MB) to leuco MB with thioglycollic acid (TGA) as a model compound of wool thiol group was investigated in the presence of copper(II) and intercuticular cementing material (δCu) extracted from wool fiber. It is confirmed that copper(II) is a catalyst for the reduction of MB and the δCu containing copper ion acts as a carrier for electron transfer.Some kerateine/δCu-immobilized hydrophilic polyurethane membranes were prepared. A conjugated redox reaction combining the reduction of MB and the oxidation of TGA was carried out across these membranes.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 27 (1988), S. 1865-1886 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The characteristics of Ca2+-binding sites and of the structural reorganization induced by Ca2+-binding in storage proteins and ion carriers are being studied as models for molecular mechanisms in Ca2+ channels and in Ca2+-dependent modulatory proteins. A first step in the study was the development of energy parameters for Ca2+ compatible with those in the CHARMM package of computer simulation software. Such parameters were obtained from an analytical fit to the potential surface for [(Ca)(OCH2)4]2+ calculated with an ab initio molecular orbital method. The resulting parametrization was tested for the hexapeptide cyclo-(Pro-Gly)3, and a 75 residue long calcium binding protein from bovine intestine (ICaBP). The geometrical parameters calculated for the hexapeptide and its 2:1 complex with Ca2+ were in good agreement with experimental data from crystallography and nmr. Similarly, the structure of ICaBP optimized with CHARMM using the new Ca2+ parameters showed good agreement with the x-ray structure both in the local structures of the calcium-binding sites and in the overall shape of the protein.
    Additional Material: 9 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 337-351 
    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 relationship between the grafting yield and the structure of graft copolymer is studied by measuring the branched chain lengths, the number of branches, the crystallinities, and the diffraction intensities of the (101) and (101) + (002) planes determined by x-ray diffraction, and the distribution of branched polymers, observed by interferometry. Over a relatively wide range of grafting yield the number of initiating sites is almost constant and about 1-2 per 2 moles of cellulose chain. Therefore, the increase of grafting yield seems to be due mainly to the propagation of branched polymers. Branched polymers are assumed to be formed in cellulose crystallites both on the normal (101) planes and in the amorphous regions of cellulose. It is found that branched polymers grow from the outer layer into the inner part of the film as the grafting yield increases. At more than 250% of grafting yield, however, branched polymers are uniformly formed throughout the layer of film in which the crystalline regions of cellulose are gradually destroyed. This result agrees with the dimensional change of gel film during the reaction. The temperature dependence of tensile strength and elongation and the wet strength of graft copolymer are also investigated. At higher grafting yields, such as 250%, the crystalline structure of cellulose is disturbed by the formation of branched polymer, and no improvement in waterproofness can be expected from grafting; the secondary bonding between branched polymers may be presumed to be same as those among cellulose. In addition, the fine cracking of the film in the burst state is found to appear more easily as the grafting yield increases, in which the aggregating state of cellulose is recognized to be changed by the formation of branched polymer.
    Additional Material: 14 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 25 (1987), S. 1431-1437 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The tetracyanoethylene anion radical (\documentclass{article}\pagestyle{empty}\begin{document}${\rm TCNE}^{ \cdot ^ - } $\end{document}) was detected by ESR spectroscopy in polytetrafluoroethylene (PTFE), which had been mechanically fractured in vacuo with tetracyanoethylene (TCNE) at 77 K. The assignment of \documentclass{article}\pagestyle{empty}\begin{document}${\rm TCNE}^{ \cdot ^ - } $\end{document} was carried out by ESR spectral simulation on the basis of an anisotropic effective hyperfine tensor that included a forbidden transition term. The \documentclass{article}\pagestyle{empty}\begin{document}${\rm TCNE}^{ \cdot ^ - } $\end{document} is formed by abstraction of an electron by TCNE from the anion that is produced by heterogeneous scission of the carbon-carbon bond in the main chain of PTFE. At least 16% of the scission of the main chains of PTFE occurs by a heterogeneous process to produce the anions. Approximately 50% of the anions decay during annealing for 30 min at 220 K in the dark, and all anions decay within 15 min at 325 K.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1307-1312 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When poly(vinylidene fluoride) (PVDF) was ground with tetracyanoethylene (TCNE) powder in a vibration glass ball mill in vacuum in the dark at 77 K, the TCNE anion radical (TCNE-) was detected in the mixture by ESR spectroscopy. The TCNE.- is formed by the abstraction of electrons by TCNE from the anion that is produced by a heterogeneous bond scission of carbon-carbon bonds in the polymer main chain. The assignment of TCNE.- was carried out by the ESR spectral simulation on the basis of an anisotropic effective hyperfine tensor that includes a forbidden transition term. At least 85% of the bond scission of the PVDF main chain is induced by a heterogeneous process to produce ionic products. The yield of these mechanions seems to increase with the polarity of carbon-carbon bond owing to a substituent group bonded to the carbon in the polymer main chain.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 16 (1982), S. 911-927 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: A long-term problem associated with total joint replacements is the formation of a fibrous tissue at the bone-cement interface which may compromise the fixation of the prosthesis. In this study, harvestable amounts of interfacial fibrous tissue were generated using a prosthetic replacement of the canine stifle joint as an animal model. The collected tissues were examined histologically and by uniaxial, unconfined compression tests. The fibrous tissue had a matlike structure. The heavy collagen fibers were distributed at random in sheets and the sheets themselves were layered to form a mat. Such a structure may be able to resist compressive stresses normal to the plane of the mat but is probably not well suited to resist shearing stresses. The fibrous tissue proved to be a very compliant, deformable material and to undergo very large strains with load. The stress-strain curve for the tissue was nonlinear and was characterized by large deformations at low loads. But with increasing loads, the material became stiffer, and at high loads, the stress-strain curve became linear with a short-term tangent modulus of 1.9 MPa at a stress level of 0.5 MPa and a compressive strain level of 50%. With regard to total joint replacement systems which consist of an outer bone shell followed by a thin layer of fibrous tissue, a mantle of PMMA cement and a central core of metal or UHMW polyethylene, the fibrous tissue is substantially more yielding and deformable than the other elements of the structure and may have a significant effect on the structural behavior of the system.
    Additional Material: 11 Ill.
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