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  • Polymer and Materials Science  (19)
  • aluminum chloride  (1)
  • infarction  (1)
  • 1
    ISSN: 1573-7365
    Keywords: focal cerebral ischemia ; hyperglycemia ; insulin ; infarction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Although it has been well established that hyperglycemia increases cerebral damage following transient cerebral ischemia, its effect on permanent focal ischemia is controversial. We hypothesized that other factors associated with hyperglycemia, such as plasma insulin, may alter the brain's response to hyperglycemia. The objective of this study was to determine if hyperglycemia changes infarction size following 8 hr of middle cerebral artery occlusion in the anesthetized cat and to examine if changes in plasma insulin levels alter hyperglycemia's effects. Infarct size in hyperglycemic cats with increased plasma insulin (38.3±8.4%, mean±SE) or in hyperglycemic cats without increased plasma insulin (30.5±7.6%) was not significantly different from that of ischemic controls (33.8±2.8%). However, the variability in infarct size tended to be greater (P=0.0647) among all hyperglycemic cats compared to control animals. The source of the variability is unknown, but this observation combined with the findings of others suggests the possibility that the effect of hyperglycemia is dependent on the exact nature of the focal ischemic insult (i.e., degree of collateral blood supply) and that this effect may vary greatly from individual to individual within a population.
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 747-753 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies on copolymerization kinetics of N-carboxyanhydride (NCA) of O-acetyl-L-tyrosine (T) with NCAs of L-valine (V) and glycine (G) were carried out in dioxane at 25°C with n-butylamine as initiator. The reactivity ratios for the VT system were found to be rV:rT:0.57:0.22; and for the GT system, rG:rT:0.26:0.42. A comparison of this data with that obtained when L-analine was used in place of L-valine or glycine showed that in the three systems, the reactivity ratio of the amino acid residue with a greater tendency to form ordered secondary structure was greater than that of its comonomer. Among the variable comonomers (glycine, L-alanine, L-valine) of O-acetyl-L-tyrosine, it is again L-alanine, whose tendency to form helical structure is very high, that has the greater reactivity ratio.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1407-1416 
    ISSN: 0887-624X
    Keywords: PBZT ; polycondensation ; tetramethylbiphenyl substituted ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(benzobisthiazole)s containing an ortho-tetramethyl substituted biphenyl moiety were synthesized via the polycondensation of 2,5-diamino-1,4-benzenedithiol dihydrochloride with 2,2′,6,6′-tetramethylbiphenyl-4,4′-dicarboxylic acid in poly(phosphoric acid) (PPA). The intrinsic viscosities of the tetramethylbiphenyl poly-(benzobisthiazole)s in chlorosulfonic acid at 30°C were in the range of 6.9-13.4 dL/g. Copolycondensation of 2,5-diamino-1,4-benzenedithiol dihydrochloride with terephthalic acid and 2,2′,6,6′-tetramethylbiphenyl-4,4′-dicarboxylic acid was carried out as well by varying the ratio of the two dicarboxylic acid monomers in the reactant mixture. The homopolymers and copolymers were characterized by Fourier transform infrared spectroscopy (FTIR) and 13C solid-state nuclear magnetic resonance spectroscopy (NMR). Thermal stability of the polymers was evaluated by thermogravimetric analysis (TGA) and thermogravimetric mass spectrum analysis (TG-MS). The tetramethylbiphenyl poly(benzobisthiazole)s were found to be more stable at elevated temperatures than the parent poly(p-phenylene benzobisthiazole) (PBZT). © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1407-1416, 1998
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 1767-1782 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In small-angle x-ray and neutron scattering studies of ion-containing polymers, it is observed that there is a maximum in the intensity and also an increase in the intensity at very low Q. Several ion clustering models have been proposed in the literature to explain the peak and the intensity increase. The SAXS data of Gierke et al. and the SANS data of Roche et al. are considered in this paper in order to elucidate the possible cluster morphology in perfluorosulfonated ionomer membranes. For these samples the occurrence of the SAXS peak is accounted for quantitatively; it is shown to arise from the interference between ionic aggregates (clusters), assuming them to be noninteracting hard spheres. In these calculations the volume fraction of the clusters (the cluster is assumed to be constituted of SO3-, a cation, and a swelling agent, which is water in the present case) is determined from water absorption values, equivalent weight, and from the density of the dry polymer. The size of the ionic clusters is chosen to match the calculated and observed peak positions. In these calculations it is assumed that all the ions are in clusters. The calculated peak value of the relative intensity invariant is found to be within ±15% of the experimentally observed intensity invariant for samples of different equivalent weight, and in different cationic form, soaked or boiled in water. Samples equilibrated at lower levels of humidity showed greater deviations. The deviations become smaller if either or both of two assumptions are made; that with a decrease in humidity (i) the percentage of clustering ions decreases, (ii) a fraction of the polymer chains is present in the clusters. This work gives credence to the thought that the small-angle scattering peak in ion-containing polymers is not a Bragg peak. This invalidates the conventional method of comparing the macroscopic and microscopic degrees of swelling. Previous SAXS work on dense groups of particles has neglected a term which is shown to be important at low angles. We found that this term is capable of qualitatively explaining the observed increase in intensity at low angles in perfluorosulfonated ionomers. The possibility of the presence of an intercluster potential, which can also contribute to the increase in intensity at these angles, is also discussed.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1881-1891 
    ISSN: 0887-6266
    Keywords: crosslinking ; poly(p-phenylene benzobis thiazole) ; PBZT ; methyl pendant PBZT ; 13C solid state NMR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to influence the compressive strength of the rigid rod polymeric fibers, methyl pendent poly(p-phenylene benzobisthiazole) fibers have been heat treated in the 400 to 550°C temperature range in air and in nitrogen for varying times to achieve intermolecular crosslinking. These fibers have been examined using Fourier transform infrared (FTIR) spectroscopy, 13C solid-state nuclear magnetic resonance (NMR) swelling behavior, and scanning electron microscopy. 13C NMR has also been carried out on solutions of as-spun fibers. Fibers heat-treated at 400°C, both in nitrogen and in air, up to heat-treatment times of 60 min are insoluble in 99% chlorosulfonic acid, however no direct evidence of crosslinking has been obtained for these fibers using spectroscopic techniques, suggesting that in these fibers the degree of crosslinking must be very low. Evidence that methyl groups are precursors to certain crosslinks was first seen via a weak methylene resonance in 13C solid-state NMR, corresponding to about 2% of the original methyl intensity, in a sample heat-treated at 450°C in air. Fibers heat-treated in nitrogen at 550°C for 10 minutes do not exhibit any swelling in chlorosulfonic acid, are brittle, have lost most methyl groups; however, some CH2 groups form. In this fiber, the carbon intensity for the CH2 group in the 13C solid-state NMR is 18% of the intensity for the CH3 group in the as-spun fiber. The fibers heat-treated at 400 and 450°C show a fibrillar morphology, while the fibrillar morphology is not observed in the fibers heat-treated at 550°C in nitrogen for 10 min. Based on this work, it is our judgment that if heat treatment of this material is to improve compressive strength, the heat treatment protocol of time and temperature will probably be critical and the highest temperatures of exposure will probably lie in the 450 to 550°C range. © 1996 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 781-787 
    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: Nitric acid etching studies have been conducted on samples of commercially available highly oriented gel-spun polyethylene fibers: SpectraTM 900 and 1000 from AlliedSignal Inc. The results show that the acid attacks the fiber, increases crystallinity as observed by X-ray diffraction, increases the enthalpy of melting of unconstrained fibers by 13-25%, and removes topological constrains thus facilitating the crystallization of chain segments in the noncrystalline regions. The acid functionalizes the fiber, creating various oxygen and nitrogen-containing moieties, specifically (C=O)—,—C=C—, and —NO2 groups. The small weight loss upon etching, less than 2%, and the fact that fibers weaken but do not fragment suggests that the gel-spun and -drawn morphology is more resistant to acid attack than are other morphologies of polyethylene. Photomicroscopy shows that acid etching opens cracks normal to the fiber axis. That the acid can attack the gel-spun fibers indicates the presence of structural imperfections such as folds, molecular kinks, or uncrystallized regions within the fibers. Infrared analysis on virgin fibers shows the absence of absorption bands normally associated with the presence of chains lying within amorphous regions in polyethylene. These and other morphological features are integrated into a description of the structure of commercial gel-spun polyethylene fibers. © 1995 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1965-1973 
    ISSN: 0887-6266
    Keywords: poly(p-phenylenebenzobisthiazole) ; Lewis acid ; Lewis base ; complexation ; mediated solubilization ; aluminum chloride ; nitromethane ; aprotic solvent ; electron donor-acceptor complex ; processing ; spectroscopic evidence ; structural changes ; stability of the complex ; decomplexation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Investigations on aluminum chloride-mediated solubilization of poly(p-phenylenebenzo-bisthiazole), PBZT, in nitromethane revealed that, in general, dilute solutions of the polymer prepared in nitromethane with a large molar excess of the Lewis acid with respect to PBZT were relatively stable and thus suitable for processing into films and coatings via regeneration with hydroxylic nosolvents while polymer solutions with minimum stoichiometrically required (PBZT:AlCl3 molar ratio 1:4) or marginal molar excess of AlCl3 relative to PBZT tended to gel during handling. Structural studies on polymer-Lewis acid complex solutions were performed using 1H and 27Al NMR. 1H NMR of the protonated structure of the model compound 2,6-diphenylbenzo [1,2-d:4,5-d′] bisthiazole was useful for confirming the 1H NMR assignments of PBZT-AlCl3 complex solution in CD3NO2. 27Al NMR was particularly useful in probing the different tetrahedrally coordinated environments of the Al nucleus in the polymer solution, pointing to a complexation interaction between the polymer molecule and the Lewis acid and also between the solvent and the Lewis acid. Direct evidence in the solid state for the presence of a reversible electron donor-acceptor complex (EDA complex) was obtained from FTIR spectra of complexed films, isolated and handled in an inert atmosphere. The structural changes upon PBZT complexation caused significant frequencly shifts in both aromatic as well as heteroring stretching modes relative to PBZT itself, and intensity variations indicative of changes in the resonance configuration between the 1,4-phenylene moiety and the aromatic heterocyclic ring were also observed upon complexation. A preliminary comparison between the pristine PBZT fibers and regenerated PBZT by dilute solution viscometry indicates that the process results, to some extent, in polymer degradation leading to a decrease in the molecular weight of the polymer © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 3057-3064 
    ISSN: 0887-6266
    Keywords: methyl-pendant PBZT ; crosslinking ; molecular modeling ; compressive strength ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Molecular mechanics and dynamics simulations have been performed on methyl-pendant PBZT to study the effects of intermolecular crosslinking. Several possible crosslinked structures were investigated. The effect of crosslinking was found to be strongly dependent upon crosslink type and, in some instances, crosslink density. A significant axial stress is predicted to occur upon the formation of phenyl-to-phenyl type crosslinks. This provides a reasonable explanation for the experimental observation of transverse cracks in the skin of crosslinked, MePBZT fiber. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 3057-3064, 1998
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 517-526 
    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: Heat treated poly(p-phenylene benzobisthiazole) (PBZT) fibers tested in tension result in two types of failure modes. In failure mode I, the fiber exhibits a relatively sharp break; mode II is characterized by significant axial fiber splitting. Approximately 20% of the fibers failed in mode II when tested at 2.54, 7.62, and 12.7 cm gage lengths. At 1.25 cm gage length all the fibers failed in mode I. Tensile strength decreased from the 1.25 to 7.62 cm gage length, but tensile strength of the fibers tested at 7.62 and 12.7 cm gage lengths were similar. The two failure mode observation is supported by the Weibull statistical distribution. Fiber tensile properties were also measured at 150°C. Axial compressive strength of the PBZT fibers as determined from the recoil test is also reported and is found to be independent of fiber tensile modulus and fiber diameter. As-received heat-treated fibers were post heat treated between 700 and 775°C. Structural changes in the fiber were studied using infrared spectroscopy, small and wide angle x-ray scattering, and swelling studies. © 1995 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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