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  • Polymer and Materials Science  (22)
  • PHYSICS, ATOMIC, MOLECULAR, AND NUCLEAR
  • 1970-1974
  • 1950-1954  (22)
  • 1954  (14)
  • 1953  (8)
Collection
Publisher
Years
  • 1970-1974
  • 1950-1954  (22)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 11 (1953), S. 225-231 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: For a particular sample of polystyrene, different osmometric estimates of Mn have been reported. The possibility that the difference is due, in the one case, to permeation of the membrane by low molecular weight polymer has been carefully considered. It is shown that this can not be the explanation. The difference is in some way associated with chemical differences in the membranes used. Apart from these considerations of error, the significance of the number-average molecular weights of the unfractionated polymers of commerce is shown to be more acutely dependent upon the detail of the low molecular weight end of the distribution than may be realized. The present calculations are based upon a realistic estimate of the low molecular weight polymer content of commercial polymers.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 10 (1953), S. 543-550 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements on flow birefringence of solutions of polyvinyl chloride in cyclohexanone revealed that the angle of orientation increases with decreasing concentration of the solution. That this surprising effect was not due to constructional or experimental errors was demonstrated by results obtained with polystyrene, which were in agreement with literature data.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 12 (1954), S. 209-219 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sedimentation constants and diffusion coefficients of sodium polymethacrylate and of polymethacrylic acid have been determined at various concentrations of polymer and of added electrolyte and the nature of the charge effects is considered. A ratio y = (molarity of added electrolyte)/(grundmolarity of polymer) is used to obtain S20 at y = ∞ when the polyelectrolyte is assumed to be uncharged. The variation of the effective radius with y is considered not to be due to asymmetry but to the open network nature of the polyelectrolyte coil.The sedimentation constant of unionized polymethacrylic acid is determined and also the variation of sedimentation constant with degree of ionization.
    Additional Material: 10 Ill.
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  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of activated fibrinogen takes place in two stages. First, the monomer units form intermediate polymers with twice the original cross-section area and about eight times the original length. The polymers have been detected under a variety of conditions between pH 6.1 and 10. The polymerization geometry is believed to be lateral dimerization with a staggered configuration, determined by a pattern of electrical charges. The negatively charged groups, though unidentified, appear to be near histidine residues, as deduced from the dependence of polymerization on pH. The positively charged groups, from this and other evidence, appear to be α-amino groups. Second, the intermediate polymers unite to form the strands of the fibrin network. This association appears to involve nonpolar groups, and the width of the final strands, unlike that of the intermediate polymer, depends markedly on the net charge as determined by the pH.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 13 (1954), S. 406-407 
    ISSN: 0022-3832
    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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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 14 (1954), S. 5-14 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that ηsp/c for a polystyrene fraction (M̄v = 250,000) in toluene decreases approximately linearly as the concentration is lowered from 1.0 to 0.1 g./100 ml. and then increases to a maximum at 0.001 g./100 ml. as the concentration is lowered still further. This increase in ηsp/c with dilution is a new effect which we ascribe to the expansion of polymer coils as well as to the disentangling of entire polymer molecules once the concentration is lowered to where there is ample room in the solution for each polymer molecule. The new techniques employ a viscometer with a flow time of 3893 seconds for toluene, special filtering of the solutions, and prolonged agitation of the solutions after each dilution. We present data to show that ηsp/c is time dependent at concentrations below 0.1 g./100 ml.
    Additional Material: 3 Ill.
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  • 7
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Relaxation distribution functions for concentrated solutions of six polyisobutylene samples, using three different solvents, have been derived from measurements by the methods of the single transducer, wave propagation, and stress relaxation following cessation of steady-state flow. The ranges of molecular weight, concentration, and temperature were about 0.3 to 2.5 × 106, 5 to 40%, and -5 to 40°C., respectively. When plotted with reduced variables with a reference state of unit density and viscosity at a standard temperature, data at different temperatures superpose; data at different concentrations superpose except for the two samples of highest molecular weight, where there are perceptible deviations. The reduced distribution functions for all the samples lie close together at long times where there is a drop associated with the finite lengths of the molecules. The theory of Rouse for viscoelastic properties of dilute solutions, when modified for concentrated solutions by assuming that all segmental mobilities are equally affected by interlacing of neighboring molecules, agrees with the reduced mechanical properties at long times fairly well. However, it does not predict the plateau region characteristic of distribution functions of polymers of high molecular weight. The existence of this plateau in concentrated solutions and undiluted polymers represents an abnormal prolongation of the longest relaxation times in these systems, which is attributed to molecular coupling by entanglement as discussed by Bueche with respect to steady flow viscosity.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 14 (1954), S. 375-384 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Evidence is discussed for and against the existence of a common meeting point when linear plots of ηsp/C against C for polystyrene in a number of solvents are extrapolated to negative concentrations. There is rather more evidence in favor than against, and most of the contrary evidence falls into a category for which exceptional behavior might be anticipated. The ordinate of the common meeting point, unlike the limiting viscosity number, is independent of solvent and is conveniently called the true limiting viscosity number [η]T. [η]T has been identified with the intrinsic configurational character of a polymer chain. The common point of intersection has the coordinates [η]T and C2, where Cx is a negative concentration. The product of [η]T and Cx has been found to be constant over a considerable molecular weight range. This leads to an expression for [η]/[η]T in terms of Huggins' k′. [η]/[η]T represents the ratio of the hydrodynamically equivalent volume of a polymer in an actual solvent to the equivalent volume of the chain in its natural state of extension. [η]T is considered in relation to [η]θ (Flory-Fox) and [η]P (Bawan). The effect of polymer heterogeneity is discussed.
    Additional Material: 3 Ill.
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  • 9
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Proteins are precipitated quantitatively from aqueous acidic solutions by polyacrylic acids (P 200-400). The highpolymer substance can be removed after dissolving the symplexes at neutral PH as an insoluble Ba- or protamine-salt, whereupon the proteins are recovered in an undenatured state. The interactions of bovine serum albumin or globulin with the polylectrolyte were studied as a function of PH and polymer/protein ratio. Mixtures of both proteins and of the whole human serum proteins can be separated at PH 4,6 by gradually adding a solution of the polymer. After centrifuging, the fractions were examined by electrophoresis on filter paper. Kidney peptidase seems to be stable under the conditions of precipitation.
    Notes: Proteine lassen sich quantitativ aus wäßriger saurer Lösung durch Polyacrylsäuren (P 200-400) ausfällen. Die Symplexe lösen sich bei neutralem PH; nach Entfernung der hochpolymeren Säure als schwerlösliches Ba- oder Protaminsalz werden die Proteine undenaturiert zurückerhalten. Untersucht wurde die Abhängigkeit der ausgefällten Protein-menge vom PH und von der zugesetzten Menge an PAcs bei reinem Serum-Albumin und Globulin (Rind), sowie an Gemischen aus beiden und an Humanserum. Unter Verwendung der Papierelektrophorese konnte die bei allmählicher Zugabe des Fällungsmittels bei PH 4, 6 eintretende Fraktionierung verfolgt werden, bei der zuerst Albumin, dann die Globuline zur Abscheidung gelangen. Vorversuche mit Nierenpeptidase zeigen, daß auch hier bei der Ausfällung kein nennenswerter Aktivitätsverlust eintritt.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 10 (1953), S. 333-344 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ribonuclease and carboxypeptidase are inactivated by ultraviolet light (2537 A.) with quantum yields of 0.03 and 0.001-0.005 respectively. The quantum yields for low molecular weight proteins are of the order of 0.03 and are higher than those for splitting peptide bonds in typical peptides (0.004-0.0004 or less). It is postulated that the primary process of inactivation involves modification of aromatic residues in proteins. A possible reason for the inverse relationship between quantum yields and molecular weights of enzymes and proteins is discussed.
    Additional Material: 8 Ill.
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