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  • Articles  (658)
  • Physics  (658)
  • 1985-1989  (113)
  • 1970-1974  (545)
  • 1935-1939
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 191-192 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 2
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is proposed here that readily observable viscous deformation is the common underlying phenomenon which is reflected in several kinds of evidence advanced for the existence of a liquid-liquid transition TLL. These include flow temperature Tf measurements, microscope hotstage coalescence, and differential scanning calorimetry (DSC) measurements. A DSC peak observed at Tg in high-molecular-weight bulk-polymerized poly(methyl methacrylate) is discussed in terms of the presence of conformations of low entropy.
    Additional Material: 3 Ill.
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  • 3
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase boundaries in the quaternary system consisting of the polymer poly(2,6-dimethyl-1,4-phenyleneoxide) (PPOPPO is a registered trademark of the General Electric Company.), the solvent trichloroethylene (TCE), and the nonsolvents 1-octanol (OcOH) and methanol (MeOH) are determined. The kinetics of crystallization are investigated by pulse-induced critical scattering. The formation and properties of PPO membranes are discussed in relation to the phase separation phenomena.
    Additional Material: 14 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 483-492 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solid-state 13C-NMR spectroscopy has been used to investigate the structure of cellulose nitrates prepared from cotton linters. The solid-state technique has the advantage that the entire range of substitution can be studied, which is not possible at present by solution methods. The spectra change progressively with increasing degree of substitution (DOS = 3 for cellulose trinitrate), and can be used to quantify the extent of substitution at C6, C2, and C3. Progressive nitration leads to elimination of the original C6 resonances of native cellulose by DOS = 1.39. The first nitration of C6 occurs in the amorphous regions, and this is complete by DOS = 0.50. Substitution at C6 is accompanied by decrystallization, as indicated by the decrease in the resonance assigned to crystalline C4, which also disappears at DOS = 1.39. A new resonance assigned to C1 appears at DOS = 0.28 at 101 ppm; the original C1 resonance for cellulose declines steadily and disappears by DOS = 2.65. This change is assigned to nitration of C2, based on the published solution spectra. Finally, development of intensity at 82 ppm at DOS = 1.83 is assigned to the effect of nitration at C3. There is no indication of any rearrangement of the unsubstituted regions analogous to those that occur on Mercerization of native cellulose.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 10 (1972), S. 2125-2134 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The validity of Silberberg's hypothesis concerning the conformation of branched polypeptides was tested by studies on solutions and on monolayers. The poly(α-amino acids) investigated consisted of poly-L-lysine backbones with side chains of poly(gamma;-benzyl L-gutamate) and poly(β-benzyl L-aspartate). In solution, the conformation was studied in the mixed solvent chloroform-dichloroacetic acid. Optical rotatory dispersion measurements demonstrated the existence of a helix-coil transition which is a function of the length of the side chain. A significant “transition curve” appeared between 9 and 15 residues. From the results, it may be assumed that the poly-L-lysine backbone is extended in a coiled conformation and the side chains are coiled or helical, depending on the number of glutamate residues. At the air-water interface, a discontinuity in the surface-pressure curve appears between 9 and 15 residues per side chain. The similarity with the results obtained in solution appears significant; however, this has to be confirmed with methods more specific for structural modifications.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2031-2043 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Farol-Weissenberg rheogoniometer has been used to follow molecular weight changes during the degradation of certain poly-α-esters in the melt state. By observing the change in melt viscosity at low shear rates it had been shown that the decomposition of the poly(isopropylidene carboxylate) is substantially first-order with respect to the molecular weight of the residual polymer. The derived kinetic parameters are in good agreement with those previously obtained by other techniques. This provides a substantial piece of supporting evidence for the view that degradation takes place predominantly by intramolecular ester interchange involving the formation of 1,1,4,4,-tetramethylglycollide. The introduction of β-chlorine atoms into the polymer structure leads to a more complex degradation pattern. Thus the presence of a single β chlorine atom per repeat unit, as in poly(3-chloro-2-methyl-2-hydroxypropionic acid) leads to a substantially similar dependence on molecular weight with the added complication of progressive crosslinking which becomes more apparent in later stages of the reaction. This crosslinking reaction plays an increasingly important part as the extent of chlorination of the polymer is increased. In addition, the presence of chlorine leads to an increased sensitivity of the degradation reaction to the presence of oxygen.
    Additional Material: 6 Ill.
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  • 7
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The bulk polymerization of acrylonitrile (AN) initiated by copper (II) nitrate, Cu(II), in the absence of light has been studied. The rate of the AN polymerization may be expressed in the Cu(II) concentration range from 5 × 10-4 to 1 × 10-1 mole 1.-1 by the equation, Rp = k5[Cu(II)]0.68, where k5 = KAN[AN]/(1 + KAN[AN]). From the spectrophotometric measurements the values of 0.70 l./mole and 0.08 l, mole were obtained for the equilibrium constant at 20 and 60°C, respectively, KAN = [C]/[AN]-[Cu(II)], corresponding to the formation of the complex C from acrylonitrile and copper (II) nitrate. An addition of triphenylphosphine (C6H5)3P into the polymerization system reduces Rp, and no polymerization takes place at all provided [(C6H5)3P]/[Cu-(II)] ≧ 5. The retardation effect of (C6H5)3P on the polymerization of AN initiated by Cu(II) is attributed to a competitive reaction of Cu(II) with (C6H5)3P in which Cu(II) is reduced and the product of this reduction CuNO3·2(C6H5)3P is inactive with respect to the polymerization of AN.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2935-2947 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: GPC chromatograms of cellulose acetate made from wood pulp customarily show a shoulder or small separate peak at the high end of the DP distribution. Material isolated from this “prehump” area is considerably enriched in mannose and xylose, and the size of the prehump in acetates from different pulps correlates with the amount of hemicellulose in the pulp. Prehump is not ordinarily found in cellulose acetate made from linters but was induced by adding mannan at the start of the acetylation, or by prolonging the acetylation beyond the time when the cellulose acetate sulfate triester is first formed. Products of poor solubility, as indicated by increased haze and false viscosity, resulted in both cases. Prehump was reduced in pulp cellulose acetate by many of the steps which give products of improved solubility: mercerization of cellulose prior to acetylation, use of more sulfuric acid catalyst, replacement of part of the acetic acid with methylene chloride during acetylation, and by removal of a small amount of high viscosity or poorly soluble material by fractional precipitation.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2991-2997 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly-3-methyl-1-butene has been synthesized by Et2AlCl/tBuCl initiator at -130°C. A cast film of this material gave three well defined crystalline phases, α, β, and γ, characterized by infrared spectroscopy. The γ polymorph could not be obtained independently of the other two. Synthesis and/or manipulative procedures that would consistently give only one of the polymorphs are still unavailable. Evidently, the three crystalline phases have very similar lattice energies, and the subtle factors that determine the ultimate nature of the crystal lattice are not yet understood.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 1759-1769 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general synthetic method and characterization of bis(ether anhydride)s, the ether containing aromatic dianhydrides of the following structure, are presented. The method involves aromatic nitro-displacement of N-substituted 3- or 4-nitrophthalimide with bisphenoxides to form N-substituted arylene-bis(phthalimido)ethers or bis(ether imide)s. Sixteen structurally different bis(ether imide)s have been prepared and subsequently converted to the corresponding bis(ether anhydride)s. Bis(ether anhydride)s are stable crystalline compounds of a moderate reactivity. Unlike highly reactive dianydrides such as pyromellitic and benzophenonetetracarboxylic dianhydrides bis(ether anhydride)s are semipermanently stable against hydrolysis in the presence of atmospheric moisture.
    Additional Material: 2 Tab.
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