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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 75 (1989), S. 335-344 
    ISSN: 1432-1106
    Keywords: Neck muscles ; Head stabilization ; Polar plots ; Electromyography ; Activation patterns
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A musculoskeletal system with more muscles than there are motions could be programmed in alternative ways to produce a single movement. In this case, the muscles would have the potential to be maximally responsive in multiple directions rather than responding preferentially in a single direction. To determine the response patterns of muscles in the head-neck motor system, the simultaneous activation of four of the 23 neck muscles acting on the head was recorded with both surface and intramuscular electrodes. Fifteen human subjects were tested during an isometric head stabilization task. When the EMG response patterns were plotted, each muscle demonstrated a preferred direction of activation. This preferred activation direction was consistent in all of the subjects for three of the muscles tested. The fourth muscle, splenius, was preferentially activated during neck flexion in half of the subjects and during neck extension in the other half. Increasing the force parameters of the task suggested a linear relationship between force and the EMG output in the preferred response directions. Responses in the nonpreferred directions were produced by a nonlinear change in EMG activation of the muscle. This finding could have implications for theories of how reciprocal activation and cocontraction patterns of response are elicited. Results from this study, that the CNS programs neck muscles to respond in specific orientations rather than generating an infinite variety of muscle patterns, are in agreement with our findings in the cat.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 83-93 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The isothermal crystallization of isotactic polypropylene at different temperatures in the presence of fibrous substrates has been investigated. It is shown that preferential transcrystalline growth occurs at the fiber surface and that changes in nucleation density in the bulk material adjacent to the fibers also occur, the extent of which is dependent on temperature and fiber volume fraction. The effects are discussed in terms of the diffusion of heterogeneities in the bulk due to interaction and the adsorption on the fibers.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 481-501 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photolysis of poly(ethylene terephthalate) films was studied in vacuo with light of wavelengths 2537 and 3130 A. A very stable filter system which cuts out the 3025 A. line was developed to isolate 3130 A. from a mercury spectrum. Despite the fact that the penetration of 2537 A. light was limited to a depth of a ca. 103 A. whereas 3130 A. light was more uniformly absorbed it was possible to demonstrate that the quantum yields for CO and CO2 formation were in agreement for the two wavelengths. Quantum yields for fractures and crosslinks were estimated by sol-gel analysis. An absorption maximum which develops near 13 μ after exposure of poly(ethylene terephthalate) to light or γ-rays was attributed to the formation of groups formed by elimination of CO and CO2. ESR spectra for trapped radicals were tentatively assigned to the components p-C6H3· and ·O—CH2—CH2—. It is suggested that the former radicals combine to form crosslinks. Quantum yields (× 104) with 3130 A. light are: CO, 6; CO2, 2; crosslinks, 5.5; trapped radicals, 1.5; With 2537 A. light, quantum yields are: CO, 6-9; CO2, 2-3; the network formed was not characterized as to crosslinks and fractures; trapped radicals were observed to exist but not determined.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 3059-3073 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Homopolymers and copolymers of fumaronitrile, maleonitrile, and succinonitrile have been prepared by using medium high temperature free-radical initiators. Black, nonfusible but soluble polymers were obtained. The spectroscopic and chemical evidence indicated a structure containing α-pyrrolenine rings and no free nitrile groups in the fumaronitrile and maleonitrile polymers and 1-pyrroline rings and free nitrile groups in the succinonitrile polymers. The polymers possessed good thermal stability, free spin concentration of 1017-1018 spins/g, and an ac conductivity at room temperature in nitrogen of 10-6 to 10-8 ohm-1 cm-1.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 429-437 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Previous studies have shown a two-peak molecular weight distribution of the grafted polystyrene side chains from preirradiation-grafted cellulose acetate. ESR has been used to investigate this grafting system in further detail. It was found that the rate of decay of the trapped radicals on adding the monomer solution was quite slow and a substantial proportion remained after 3 days at 25°C. The G value for radicals lost was, however, in good agreement with the G (grafted side chains) produced during the same period. The ESR spectrum does not change on addition of the monomer solution. The explanation offered is that the side chains grow and terminate rapidly compared with the slow overall rate of decay. The grafting yield and the molecular weight of the grafted side chains continue to grow until the reaction is terminated, leading perhaps to the high molecular weight narrow distribution fraction.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2703-2711 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Exposure of poly(ethylene terephthalate) to γ-rays results in the formation of radical I, radical II (tentatively), and to an unassigned radical (III) which is responsible for a central peak in the ESR spectrum. It is believed that completely amorphous samples of polymer contain radicals II and III. On heating, the radicals decay, and the relative proportion of radical III increases. The kinetics of the overall decay process were followed by measuring the decrease in peak height with time. After an initially rapid reaction the decay of the radical population conformed to second order kinetics. An Arrhenius plot of the logarithm of specific rate versus 1/T indicated two lines which intersected at 72°C, which is close to the glass transition temperature. The activation energies were 112 kcal/mole above 72° and roughly 25 kcal/mole below 72°C. Reference to reports in the literature suggests that this decay can be explained by long-range movement of the polymer molecules, even in the glassy solid. The decay of radical I in the crystalline regions of an oriented sample was shown to follow first-order kinetics. As the decay occurs at temperatures as low as 100°C (the melting point is about 260°C), it seems that decay by normal physical movement is unlikely. The results might be explained by invoking the hypothesis of chemical migration of free radical sites by hydrogen atom hopping.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 2199-2201 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No. Abstract.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Free radicals formed by γ-irradiation of oriented samples of poly(ethylene terephthalate) (PET) were studied at 25°C. by ESR spectroscopy. The G value for trapped free radicals is 0.02. The predominant radical is identified as $\text{O} - \text{\underset{\raise0.3em\hbox{$\smash{\scriptscriptstyle\cdot}$}}{C} H} - \text{CH}_\text{2} - \text{O} -$, and a minor component of the spectrum is tentatively assigned to the radical —CO—Ċ6H3—CO—. The absence of cyclohexadienyl type radicals is discussed. Previously reported dose rate effects in PET are explained by reference to a chain reaction involving β-bond scission of the radical $\text{O} - \text{\underset{\raise0.3em\hbox{$\smash{\scriptscriptstyle\cdot}$}}{C} H} - \text{CH}_\text{2} - \text{O} -$.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 1197-1202 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methyl methacrylate may be polymerized by free-radical initiators in liquid sulfur dioxide without incorporating sulfur dioxide in the polymer chain, even though methacrylate radicals and sulfur dioxide readily as indicated by electron spin resonance studies. An explanation for this anomalous result is advanced, and evidence for the participation of sulfur dioxide in the transition state of the addition reaction is presented.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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