Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Electronic Resource  (8)
  • Chemistry  (8)
Material
  • Electronic Resource  (8)
Years
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 293-310 
    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 tendency of a plasticizer to resist exudation from poly(vinyl chloride) (PVC) under compressive stress, known technologically as “compatibility,” is treated in terms of a network model, the plasticized composition being thought of as a rubber crosslinked by crystallites. Compatibility is increased by increased solvency (Flory-Huggins χ) and decreased by increasing plasticizer molar volume. A large crosslink density and/or insufficient melting of crosslinks during processing (thermal history) also decreases compatibility. All commercial primary plasticizers are believed to be infinitely miscible with amorphous PVC. Phase separation which occurs is syneresis and not related to any phase diagram. Swelling tests for compatibility and swelling measurements on dilute PVC gels are described. Some general principles relating to gel formation and association in polymer solutions are also discussed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 203-213 
    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: Density gradient sedimentation of polystyrenes, Hevea rubber and synthetic cis-1,4-polyisoprene was studied in the systems ethylene bromide-mesitylene and (1,2-dibromo-1,1-difluoroethane)-cyclohexene. The latter system has very closely matched refractive indices at atmospheric pressure. This work was oriented toward the analysis of mixed polymer and copolymers. Large density gradients were used with schlieren optics. No difference between the points of accumulation of polystyrene from different types of polymerization nor between Hevea and cis-polyisoprene could be found under the conditions employed. Narrow gradient patterns could be produced for polymers of Mv = 200,000. These broadened with increasing polymer concentration. At M = 106 it is believed to be possible to estimate semiquantitatively concentrations of polystyrene of 5 ppm. A method of estimating the amount of a component present in terms of its gradient pattern is given. The density distribution in the bromofluoroethane system was studied by the use of inert marker substances of known density.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 5 (1950), S. 739-741 
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Intrinsic viscosities of dextrans of known branching ratio were measured in water formamide, and in a water-methanol mixture at two temperatures. Weight-average molecular weights (sedimentation equilibrium) ranged from 1.1 × 104 to 1.7 × 106. A model for the hydrolyzed dextran molecule was assumed. Using the methods of Zimm and Stockmayer, the g factor calculated from this model was compared with the g factor obtained from the intrinsic viscosity-molecular weight data through the use of the Flory-Fox theory (g = ratio of squares of radii of gyration of branched to unbranched polymer). The calculated branch lengths required to make consistent the g factors obtained by two different routes were of the same order of magnitude as those found by classical organic chemical methods for other dextran preparations. The intrinsic viscosity-molecular weight relation at 25°C. in water for linear dextran was predicted from the data. It is suggested that investigations of branched polymers of known constitution be carried out by these methods.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 13 (1954), S. 460-460 
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 62 (1962), S. 179-196 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is outlined for the determination of molecular weights and molecular weight distributions in linear, neutral polymers from boundary spreading data obtained from the ultracentrifuge. By use of the intrinsic viscosity, and having knowledge of its molecular weight dependence, it is possible to avoid calibration of the method with fractions of known molecular weight. Because of a maximum sensitivity of sedimentation coefficient to molecular weight, and only small concentration dependence of the sedimentation coefficient, theta solvents are preferred for these measurements. Corrections are made for pressure dependence of the sedimentation rate. The method is illustrated by measurements on polystyrenes in cyclohexane at 34°C. Comparison is made with precipitation chromatography data. Because of the number of experiments which must be made in order to extrapolate data to infinite dilution (each experiment consisting of at least four schlieren diagrams) this type of analysis probably involves as much labor as precipitation chromatography.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 14 (1954), S. 81-86 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Data for a number of vinyl polymer-solvent systems show that the constant Ks in the relation 1/S = (1/S0) (1 + KsC) (where S and S0 are sedimentation constants at the concentration C and zero respectively) is proportional to the intrinsic viscosity. The average constant of proportionality is 1.6. Assuming the Mandelkern-Flory theory of the relation of frictional coefficient and intrinsic viscosity to root-mean-square end-to-end distance and Burgers' relation for the sedimentation constant of a dilute suspension of spheres, the ratio Ks/[η] is calculated to be 1.66. Molecular weights may be calculated from Ks and the limiting sedimentation constant, S0 without the use of the constants Φ and P, and agree well with molecular weights determined independently. These considerations apparently do not apply to cellulose derivatives, for which Ks is not proportional to [η].
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 449-456 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sedimentation equilibrium of polymers in mixed solvents at infinite dilution of polymer was analyzed by thermodynamic methods equivalent to those used by Stockmayer and Kirkwood and Goldberg for the light scattering case. It was found that the apparent weight-average molecular weight in a binary solvent mixture (when nonrefractometric methods are used to measure the experimental concentration gradient) is formally identical with that derived by Lansing and Kraemer on the assumption of stoichiometric combination of one of the solvents with the polymer. The “solvation number” now actually measures a preference for one solvent and can be expressed in terms of thermodynamic quantities characteristic of the ternary polymer-solvent system. In the case of refractometric measurements, where the two solvents have different refractive indices, refraction terms similar to those encountered in light scattering theory for mixed solvents also enter. Under equilibrium conditions, for polymer solutions in pure solvents, thermodynamics can say nothing about “solvation,” which is inseparable from the over-all nonideal behavior at finite concentrations. There is strong reason to believe that all types of experiments designed to measure solvation in mixed solvents under equilibrium conditions must give the same answer, since the same thermodynamic quantities determine polymer-solvent interactions in all cases. By assuming a dynamic equilibrium between sedimentation and diffusion in the equilibrium case and using the sedimentation term for the sedimentation velocity case, an expression for the sedimentation constant in mixed solvents at infinite dilution of polymer has been obtained. This expression is almost the same as that previously derived by Schachman and Lauffer, the difference occurring in an assumption about the density of solvated liquid made by these authors.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...