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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2221-2238 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies have been made of the photochemistry of ethylene copolymers with carbon monoxide (CO), methyl vinyl ketone (MVK), and methyl isopropenyl ketone (MIPK) in solid films. Infrared (IR) evidence is presented to show that a variety of unexpected ketone structures is present in these polymers as a result of 1,5-hydrogen transfer or “back-biting” during the high-pressure polymerization reaction. These additional structures complicate the analysis of the quantum yield data. The overall quantum yield for carbonyl disappearance (φ-co) which increases from 0.074 to 0.24 to 0.26 in the series PE-1% CO, PE-2% MVK, and PE-20% MIPK reflects the increasing stability of the alkyl radicals produced from the type I process in the respective ketone structures. It is also shown that ketone groups located in the backbone of the polymer, as in the 1% CO copolymer, have lower quantum yields for photochemical reactions, particularly those that produce free radical intermediates. Studies of the gaseous products from extensive photodegradation under nitrogen show that in all three cases carbon monoxide is the major product (46-65% of the total). Acetaldehyde and methane, expected from the type I reaction, are major products only for the MVK and MIPK copolymers. Reaction schemes are presented to explain the major products observed.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1111-1116 
    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: Proton spin magnetization relaxation in the rotating frame is a simple exponential for poly(2,6-dimethylphenyleneether) (PPO) (23K)/polystyrene (PS) (9K) blends of various compositions; these blends are truly homogeneous at the spin-diffusion distance scale of a few nanometers. Blends of PPO with high molecular weight PS exhibit nonexponential decays for the PS component but exponential decays for the PPO component, indicating compositional fluctuation for PS. In some blends, the relaxations are nonexponential for both components. Three factors have been identified to promote microheterogeneity of nanometer dimensions: high polymer molecular weight, increase of temperature, and preparation of blend using solvent that induces crystallization of PPO such as toluene.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 247 (1997), S. 239-253 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Aliphatic polyesters are more or less hydrolytically degradable, depending on their chemical, configurational and morphological structures. Hydrolysis can be either homogeneous or heterogeneous, depending on many structural and environmental factors. The present understanding of this hydrolytic degradation is recalled. The importance of diffusion-reaction phenomena is discussed on the basis of the behaviors of polyesters derived from α-hydroxy acids, namely lactic and glycolic acids and attempts are made to extend the understanding to other members of the aliphatic polyester family. The main results of some recent investigations of the effects on poly(lactic acid) polymers of basic additives and of initiators such as stannous octoate and zinc metal, which are now industrially used, are presented.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 2295-2302 
    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 fate of a racemic lactic acid polymer (PLA50) was investigated by allowing parallelepiped plates of PLA50 to age in liquid medium containing a mixed culture of Fusarium moniliforme and Pseudomonas putida at 30°C. Microbial activity was monitored by measuring pH, lactic acid formation by high-performance liquid chromatography, and esterase activity in supernatant. Degradation of the plates was monitored by weighing, size exclusion chromatography, and visual examination. Under the selected conditions, pH increased up to 8, whereas it remained constant in the microorganism-free control. No significant lactic acid formation or esterase activity was detected in the supernatant during the experimental period (32 weeks). For the first 17 weeks, the water absorption rate of the plates was the same in both the microbial and the control media. Subsequently, plates absorbed more water in microbial than in control media. Typical surface/center differential degradation of plates was observed until 17 weeks, but it reduced progressively. At 32 weeks, specimens appeared completely disintegrated in the microbial medium. PLA50 plates were also buried in the soil for 8 weeks. After recovery, plates were allowed to degrade 8 weeks under controlled conditions. Scanning electron microscopy of these plates showed the development of some filamentous fungi at the surface and into the bulk of plates. Five fungal strains were isolated which appeared to be able to assimilate PLA50 oligomers in mixed cultures. It was assumed that PLA50 plates had been first degraded by chemical hydrolysis, followed by the bioassimilation of degradation by-products in both experiments. © 1996 John Wiley & Sons. Inc.
    Additional Material: 9 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 1159-1164 
    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 effect of interaction between carbon black and polymer on electrical behavior was studied using the ESR method. The polymer matrices used were HDPE, LDPE, and ethylene/vinyl acetate (EVA). Two kinds of carbon blacks (CB), high structure CSF-III and low structure FEF, were used as a conductive filler. Compared to that of the HDPE/FEF compound, the positive temperature coefficient (PTC) intensity is lower and electrical reproducibility is worse for the HDPE/CSF-III compound; however, it can be improved significantly by radiation cross-linking. On the other hand, the cross-linking has no practical effect on the PTC intensity of the LDPE/CSF-III compound while it can be achieved by mixing the compound for a longer time. The great PTC intensity was obtained in the HDPE/EVA/CSF-III compound, and it is greater than that of HDPE/CSF-III or EVA/CSF-III. We explain these results using the concept of interaction between the filler and matrix. The absorption of the polymer on the carbon black surface may be physical or chemical; the latter is caused by the free-radical reaction between the polymer and carbon black, and it can occur during the radiation or preparation process of the compound. These “bound polymers” are essentially important for materials to have a great PTC intensity and good reproducibility. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 607-613 
    ISSN: 0887-6266
    Keywords: solid NMR ; PPO ; HIPS ; SBS ; blends ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solid-state NMR relaxation has been used to explore the distribution of components in poly(phenylene oxide) (PPO) high impact polystyrene (HIPS) and PPO/poly(styrene-b-butadiene-b-styrene) (SBS) blends. The nuclear relaxation of PPO in the former system is single exponential for all compositions, but the relaxation of PS in the blend is simple exponential only when the PPO content is low but is otherwise nonexponential. The nuclear magnetization decay curves were analyzed in terms of statistical compositional fluctuation at the scale of spin diffusion distances of several nm. Distribution functions for nuclear relaxation and for blend composition have been derived. Extraction of low molecular weight occluded PS from HIPS resulted in blends having reduced homogeneity. Addition of low molecular weight PS enhanced homogeneity in both the PPO/HIPS and PPO/SBS blends. © 1994 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2935-2943 
    ISSN: 0887-6266
    Keywords: polymer blend ; extrusion ; light scattering ; optical microscopy ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A light-scattering photometer with optical microscope for in-line studies during polymer processing is described. The instrument utilizes a commercial twin-screw extruding device that feeds molten polymer into a narrow slit die equipped with sapphire optical windows. The flow rate through the die is controlled via the feed rate, screw rate, and a by-pass valve. The optics for light scattering and microscopy can be switched back and forth via simple translation of a rail-mounted optical platform without realignment, allowing efficient in situ morphological studies in both real and reciprocal space. Extruded polystyrene/polyethylene blends and melts are used to demonstrate the performance and versatility of the instrument. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2935-2943, 1997
    Additional Material: 12 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 403-409 
    ISSN: 0887-6266
    Keywords: polyimides ; Kapton ; Upilex ; water absorption ; 1H, 2H and 17O NMR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Commercial polyimide films containing up to ∼ 3 wt % water have been studied by proton, deuteron, and oxygen-17 nuclear magnetic resonance (NMR). Comparisons between NMR results and previous dielectric relaxation (DR) results for a variety of Kapton films show that there is a one-to-one correspondence between specific dielectric loss peaks and features of the 2H or 17O NMR spectra. It is concluded that water molecules, which interact only weakly with the polymer, reside in the polyimide matrix in two configurations, randomly oriented single molecules and chains of water molecules oriented perpendicular to the plane of the film. The correspondence between NMR and DR observed in water in Kapton extends to water in Upilex and to methanol and acetic acid in Kapton. © 1995 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2579-2589 
    ISSN: 0887-6266
    Keywords: starch ; solution-gel ; water sorption ; unfreezable water ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The water sorption of several starch samples and resistant starch (RS) samples were analyzed using an equilibrium solution-gel structure model and the results were compared to various sorption theories. It is found that the water sorption relations to water activity in starch in the high water content region could be properly described by the equilibrium two-phase structural model. The results suggested that favorable starch-starch interaction determined the formation of starch gel in water. The gel structure had a high molecular modulus of 108 Pa and thus had limited water sorption capability. Part of the starch also exhibited the solution properties with water due to chain ends and defects of the gel structure. Despite the unfavorable starch-water interaction, starch-water solution might be formed due to the predominant contributions from the entropy of mixing. The solution phase was responsible for the rapid increase of water sorption at high water activity. It was also demonstrated that the starch could maintain a maximum dynamic unfreezable water up to ≈ 36%, which was consistent with the DSC measurements. © 1996 John Wiley & Sons, Inc.
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