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  • Articles  (848)
  • Chemistry  (848)
  • AERODYNAMICS
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  • 2020-2023
  • 1960-1964  (848)
  • 1925-1929
  • 1963  (848)
  • Physics  (848)
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  • Articles  (848)
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  • 2020-2023
  • 1960-1964  (848)
  • 1925-1929
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  • 101
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 32-36 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: An expression for the “average” viscosity of a polymeric material realized during an injection molding shot is developed. From this expression certain rheological quantities are taken which should better express ease of molding than do conventional testing methods. Comparison is made between actual molding experience and quality as predicted by the new method.
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  • 102
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 67-70 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Methacryloyl chloride was polymerized in a number of solvents, and the polyacid chloride was converted into the methyl ester. The yield and viscometric molecular weight are given for each sample, whereas the osmometric molecular weight is given for selected samples. The choice of solvent controls the degree of polymerization between the limits of 500 and 8,800. Polymer yields were about 20% and the degree of polymerization was 1500 when dioxane was used as a solvent, whereas the yield increased to 45% and the DP was very high when such solvents as cyclohexane and n-hexane were used. Polymerization in solvent mixtures gave intermediate molecular weight values. Infrared analysis showed the presence of anhydride.
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  • 103
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 201-209 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 application of a free vibration technique to the study of the cross-linking of an epoxy resin by an amine is demonstrated. Curing curves are presented showing the changes in dynamic mechanical flexural modulus and damping during reaction. At room temperature, the glass transition point is reached after a conversion of about 65% of the epoxide groups. Comparisons of the dynamic mechanical and infrared curing curves indicate a lowering of the reaction rate after this point is reached. Finally, an activation energy for the epoxy-amine cross-linking reaction is calculated.
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  • 104
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 220-224 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: 1,2,2,-Trifluorovinyl phenyl ether and 2,3,4,5,6,-pentafluorophenyl 1,2,2-trifluorovinyl ethers have been prepared, and the nucleophilic reactions of the phenoxide and 2,3,4,5-pentafluorophenoxide salts with tetrafluoroethylene have been investigated. In general, it is some-what difficult to control the reaction so as to produce the desired olefinic monomer. Under truly anhydrous conditions and when other sources of active protons are avoided, the olefin is the chief product if excess tetrafluoroethylene is used. The monomer produced is very reactive with phenoxide ions, and the diphenoxyolefins are the chief secondary products. Both monomers failed to polymerize under normal, free radical conditions. With boron trifluoride an oily material was obtained from the trifluorovinyl phenyl ether. High pressure and gamma rays converted both monomers into polymers.
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  • 105
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 234-234 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: No Abstracts.
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  • 106
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 231-234 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 polymer was prepared by pyrolyzing the sodium salt of 3,5,7,8,-tetrachloroperfluoro-octanoic acid and subsequent dechlorination of the resulting heptene with activated zinc. The heptadiene was separated from other dechlorination products and brought to a high degree of purity through use of vapor phase chromatography and polymerized in bulk utilizing gamma rays at room temperature, 100°C and 150°C, and utilizing ultraviolet light at 150°C. The properties of these brittle and glossy polymers were determined. Also the purified 4-chloroperfluoroheptadiene-1,6 was telomerized with dibromodifluoromethane yielding a cycle, clear, colorless, liquid telomer.
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  • 107
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963) 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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
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  • 108
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 236-237 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: No Abstracts.
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  • 109
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 238-250 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: A determination of the performance indices of ablative plastics is indeed a formidable task because of the severity of the high-temperature test environment, nonstandard test methods, limitations of available evaluation facilities and the complex interrelationship between materials performance and environmental parameters. In spite of these difficulties, considerable progress has been made in establishing new test methods for evaluating very high-temperature (ablative) plastics. This article describes the test facilities and measurement techniques available for obtaining research and design data on ablative plastics.
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  • 110
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 251-259 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 influence of bulk physical properties on the bond strength of an adhesive was studied. A conventional epoxy resin when cured with various mixtures of phthalic acid and anhydride exhibits maximum bond strength when the curing agent is 75% acid and 25% anhydride. This effect is explained on the basis of physical properties of the unfilled resin systems. Most significant of these were the heat distortion temperature and the compressive break and yield strengths.
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  • 111
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 383-391 
    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: A homologous series of polyoxymethylene di-isopropyl ethers [R—O(CH2O)n—R] from n = 1 through n = 6 has been prepared and characterized by gas/liquid partition chromatography, infrared spectroscopy, and other techniques. The acid hydrolyses of the series indicated no rate dependence on chain length between the endgroups, which suggests that the rate of hydrolysis is not dependent on the remaining intermediate group. The rate constants and activation energy are reported, as well as those from the literature. The conclusion is reached that hydrolytic degradation studies of formaldehyde-crosslinked cellulose cannot yield information on the chain lengths of the crosslinks.
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  • 112
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 357-374 
    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 modification of cellulose (cotton fabric or yarn) has been carried out with acrylonitrile under ionizing radiation. Irradiation of the cotton in aqueous acrylonitrile solutions with gamma- or electron radiation produces a modified cotton with improved rot and mildew resistance similar to that of cyanoethylated cotton. Strength properties are not significantly affected, provided the radiation dose is less than 5 Mrads. The pickup of acrylonitrile by cotton depends on monomer concentration, dose, and dose rate. It was also observed that water was necessary to give the desired uniform modification. Doses of 0.5-1.5 Mrads produced modifications in the range of 8-15%. Dose rate effects are present at low doses, where pickup decreases with increasing dose rate. Above 5 Mrads, dose rate effects are minimized. Although the data do not show whether actual grafting is occurring with the cellulose, either directly from radiation or through oxidative products formed in the water, or whether the cellulose is being swollen with the aqueous monomer solution which is then intimately polymerized by radiation fragments resulting from the radiation, it is apparent that polymer is formed uniformly upon or within the cellulose structure and that it cannot be removed by solvent extraction. As a result of the modification, the solubility of the cellulose in its usual solvents is decreased and other properties are modified, especially rot resistance, which is improved. Modification of cotton with monomers other than acrylonitrile has also been considered. Pickups of styrene, acrylic acid, methyl isopropenyl ketone, ethyl acrylate, and methyl methacrylate have been obtained from methanol-water solutions.
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  • 113
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. S2 
    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
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  • 114
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. S1 
    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
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  • 115
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. S2 
    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
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  • 116
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 443-450 
    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 characteristics of the cold-drawing of Lexan polycarbonate are compared with the several proposed mechanisms of cold-drawing. It is concluded that the mechanism of Lazurkin and Fogel'son, involving biased segmental motion, is correct. It is indicated that this mechanism easily explains the neck formation, and it is suggested how the glass temperature enters into cold drawing.
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  • 117
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 451-459 
    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 reactivity ratios in the copolymerizations of N-tert-octyl acrylamide, N-n-octyl acrylamide, and N,N-di-n-butyl acrylamide with styrene and methyl methacrylate have been determined, and the Alfrey-Price Q and e values calculated. The distributed monomer N,N-di-n-butyl acrylamide was found to be more reactive than either N-n-octyl or N-tert-octyl acrylamide, which were of about the same reactivity.
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  • 118
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 399-410 
    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: A method of treating experimental flow measurements on high polymers to obtain the basic shear diagram is described. Shear stress data are corrected to eliminate capillary end effects, and shear rate data are modified for the non-Newtonian behavior of the materials. Differences in flow behavior of commercial low-density polyethylenes are illustrated, and the effects of the two corrections are demonstrated. The method is applicable to other polymer melts. Although the data could be expressed by the power law, the fact that logarithmic plots of shear stress versus shear rate are not linear suggests that such relationships would be approximate. The data are expressed better by the threeconstant Powell-Eyring equation, although the significance of the three parameters is uncertain. The need to obtain the rheological constants from the basic shear diagram rather than from an uncorrected or partially corrected capillary flow diagram is emphasized. In support of previous investigators, irregularities in the extrudate were observed at high shear stresses. However, it was not possible to determine at what pressure the roughness was initiated. The shear diagrams calculated from the experimental data do not exhibit any point of inflection as reported in some studies.
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  • 119
    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: A study of 11 variables of a modacrylic-fiber wet-spinning process has shown that the tenacity and stiffness modulus of the fiber depend primarily on the amount of stretch imparted during spinning and the solvent content of the tow at the time of stretching. The solvent content governs the degree of plasticity of the fiber during stretching and hence the degree of orientation achieved at a given stretch ratio. The solvent content, in turn, is determined primarily by the specific surface (fiber area per unit volume) through which solvent diffuses out of the fiber into the coagulating bath. As a result, the tenacity and stiffness modulus are invesely related to the denier per filament in the coagulating bath prior to stretching. The denier of the filament in the coagulating bath is determined by the concentration of fiber resin in the spinning solution, the volume of solution extruded per unit time, the velocity with which the fiber is withdrawn from the coagulating bath, and the number of holes in the spinnerette. These fundamental variables, along with stretch, determine the tenacity and stiffness of the spun fiber. The only other variable studied that affected the fiber physical properties was the drying temperature. Increasing the temperature slightly reduces both fiber tenacity and elongation. Variables having no influence on the mechanical properties over the range studied include length, temperature, and solvent concentration of the coagulating bath, residence time of the filaments in the coagulating bath, relaxation applied after stretching, and shear rate at which the spinning solution is extruded through the spinnerette orifices.
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  • 120
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 461-468 
    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 changes in solvent resistance and solution viscosity of polyethylene glycol and polypropylene glycol after heating with dicumyl peroxide at 140°C. are consistent with crosslinking of the former and degradation of the latter. Analytical work showed that in both cases all of the peroxide decomposed could be accounted for acetophenone and cumyl alcohol. In the case of polyethylene glycol, crosslinking results from abstraction of secondary hydrogen atoms and dimerization of the resulting radicals; in the case of polypropylene glycol abstraction of tertiary hydrogen atoms leads to radicals which break down by scission at a C—O bond to give a ketone and a more stable radical. This latter process proceeds with an efficiency of unity.
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  • 121
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 469-474 
    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: Molecular weights of polytetrafluoroethylene are presently measured by a density method. We have found that polytetrafluoroethylene exhibits a sharply defined maximum relaxation time, τm, above its melting point. There is a clear correlation between τm at 380°C. and the “molecular weight” Mn of the polymer based on the measurement of density. However, log τm vs. log Mn gives a slope of 0.78 as against a value of 3.4 obtained for other polymers. Either polytetrafluoroethylene has flow behavior very different from other polymers or the molecular weight of the polymer based on the measurement of density is only approximate.
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  • 122
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    Journal of Applied Polymer Science 7 (1963), S. 475-491 
    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: In the present paper different views concerning polymer-to-polymer adhesion were considered and the theory suggested whereby adhesion of high polymers as well as autohesion is reduced to diffusion of chain molecules or their segments and to the formation of a sturdy bond between the adhesive and the adherend as a result. From the viewpoint of the suggested theory the influence of such factors as the duration of contact between the adhesive and the adherend, contact temperature, molecular weight of the adhesive, shape and polarity of macromolecules, and phase state of polymers was considered and explained.
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  • 123
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. S3 
    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
    Additional Material: 3 Ill.
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  • 124
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    Journal of Applied Polymer Science 7 (1963), S. 753-782 
    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: Chloromethylstyrene monomer was grafted to 3 denier (preformed) polypropylene fibers by using ionizing radiation. At elevated temperatures, microscopical investigations of changes in diameter and in birefringence demonstrated that this monomer swells the fibers without dissolving them. Thus, it is comparatively simple to achieve grafting all the way to the center. Such grafted fibers can be dyed by direct or acid dyes in non-aqueous baths (e.g., dimethylformamide at 210°C.) using levels of graft of ∼25% by weight. This leads to covalent bonding arising from reaction between the dye and the benzyl chloride group of the graft. Dyeing in standard aqueous baths can also be achieved at even lower levels of graft (less than 10% by weight) if the grafted material is treated with a nucleophilic reagent such as pyridine. Using thin cross sections of treated fibers, photomicrographs were taken with monochromatic UV radiation, and with visible light on color film. These, combined with electron micrographs of much thinner cross sections provide pictorial proof of the complete penetration of the graft and of the dyes as well as showing the opening up of the structure effected by grafting. By the means employed, it was possible to achieve marked improvements in dyeability, sticking temperature, moisture regain, and antistatic behavior without diminishing the excellent mechanical properties of the polypropylene fibers.
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  • 125
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    Journal of Applied Polymer Science 7 (1963), S. 783-787 
    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: Monomers of vinyl formate, vinyl acetate, vinyl propionate, and vinyl butyrate were carefully purified by distillation in a Vigreux column and in a 56-plate glass helixpacked Todd column. The refractive indices and boiling points of the purified monomers agreed with those given in the literature. The purified samples were exposed to the radiation of a quartz mercury lamp in order to produce several per cent polymer. The refractive indices are tabulated and plotted in graphs.
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  • 126
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    Journal of Applied Polymer Science 7 (1963), S. S7 
    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
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  • 127
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    Journal of Applied Polymer Science 7 (1963), S. S11 
    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
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  • 128
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    Journal of Applied Polymer Science 7 (1963), S. S9 
    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
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  • 129
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    Journal of Applied Polymer Science 7 (1963), S. 789-801 
    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 solubility and the volatile product yields after oxidation from rubber vulcanized, with sulfur accelerated with an MBT-selfenamide have been compared with the same quantities for peroxide and TMTD vulcanizates. No significant difference was found. It is concluded that the chain scission mechanism is independent of the nature of the crosslinking.
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  • 130
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    Journal of Applied Polymer Science 7 (1963), S. 817-832 
    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: A series of thirteen polyethylene and ten polypropylene packaging films was studied by both the Handle-O-Meter and the dynamic tensile modulus apparatus, to discover how the stiffness of polyolefin films determined with the Handle-O-Meter depended on the modulus of the material and the thickness of the film. The polyethylene films included low-, medium-, and high-density resins and ranged in thickness from 0.7 to 4 mils. The moduli of these films ranged from 2.5 X 109 to 18 X 109 dynes/cm.2 The polypropylene films were made from several types of resins with moduli varying from 73 x 109 to 54 X 109, and the thicknesses of these films ranged from 0.5 to 4 mils. When the logarithm of the ratio of stiffness to modulus was plotted as a function of the logarithm of the thickness of the film, as determined from unit weights and densities, a straight line was obtained with a slope of 2.5. This means that over a wide range of gauge and modulus the Handle-O-Meter stiffness of these materials, S (in grams), is related to the modulus, E (in dynes per square centimeter), and the thickness, t (in mils), by the equation S = 1.41 X 10-9Et2.5. This result, which shows that the Handle-O-Meter stiffness of polyolefin films may be represented as a function of the thickness and the modulus as given by the dynamic tensile modulus apparatus, may be used to calculate a modulus value from any single Handle-O-Meter stiffness value or, alternatively, to reduce Handle-O-Meter stiffness measurements to a standard thickness. Conversely, this relationship may be used to predict the Handle-O-Meter stiffness of a film made from a polymer whose modulus is known.
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  • 131
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    Journal of Applied Polymer Science 7 (1963), S. 803-815 
    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: Wakelin's method of correlation analysis of x-ray diffraction patterns was adapted for fibers, films, and polymer samples of poly(ethylene terephthalate). This method gives a number called a crystallinity index, which is a measure of how far an unknown sample is between the extremes of the most amorphous and most crystalline samples obtainable for a polymer species. By being relative, this index eliminates the controversial assumptions of absolute crystallinity determinations. It is especially suited for routine studies since the calculations are readily adapted to the use of a computer and since the total time needed to obtain an index is short. A study of the indices of a variety of poly(ethylene terephthalate) materials produced the following conclusions:(1) Maximum crystallization is achieved only by starting with an unoriented amorphous film. This is contrary to the view that orientation helps crystallization. Also, this shows that the act of spinning a fiber sets up an apparently strained state which will not crystallize to the same high level as a cast film. (2) Time of heating can be exchanged for temperature of heating, since the rate of crystallization is slow for this polymer. Thus, a longer time at a lower temperature is the equivalent of a shorter time at a higher temperature in producing equivalent crystallinities. (3) The crystallinity measured by density is not the same as the crystallinity measured by x-rays. (4) A preordered state must exist in fibers in which segments of molecules have lost their complete randomness and are densely packed, yet the segments are not perfectly enough placed to produce x-ray diffraction. Or, it can be concluded that spinning or drawing disrupts the fiber's perfect lattice so that less x-ray diffraction is produced than the high density would indicate.
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  • 132
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    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: Batch copolymers, made by polymerizing acrylonitrile, vinyl acetate, and 2-methyl-5-vinylpyridine (MVP) with a chlorate-sulfite redox catalyst, are fractionated with respect to MVP content when they are fractionated with respect to molecular weight or polymer grain size. Polymer fractions of lowest molecular weight or smallest grain size contain the most MVP. A mechanism is proposed to explain these facts. To test the proposed mechanism, both ultraviolet and electron microscopes are used to study polymer formed during the early stages of batch polymerization. The effects of adding MVP, and of total monomer concentration, on the particles formed are determined. Interpretations of the microscopical observations are compared with the chemical interpretation. When MVP is present, the initial particles formed are more soluble, form colloidal particles less readily, and stabilize the colloidal particles, if formed, due to the charges on the polymer Initial particles with highest MVP content form polymer of lowest molecular weight and aggregate into the smallest polymer grains.
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  • 133
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Non-Newtonian flow of moderately concentrated solutions of polyvinyl alcohol (PVA) in water and polystyrene (PS) in toluene were measured with a Maron-Krieger-Sisko viscometer at various temperatures and concentrations. The usual dependences of the apparent and zero shear viscosities for two polymers on rate of shear, temperature, and molecular weight have been found. The log-log plot of zero-shear viscosity versus concentration can be represented by two straight lines intersecting at one point (critical concentration cc). The critical concentration in volume fraction of polymer, v2c, multiplied by the chain length Z is not constant but decreases with decreasing Z, although it has the same order of magnitude as the value of Zcv2 obtained from the log-log plots of viscosity versus Z for many systems of polar and nonpolar polymers. The product ccρZ1/2 (ρ = density of the solution) is constant and independent of Z. To explain the constancy of this product, an equivalent sphere model is presented. When the volume fraction of spheres is assumed to be unity, the extension of molecules agrees very well with the unperturbed extension evaluated from intrinsic viscosity data in ⊖ solvent.
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  • 134
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    Journal of Applied Polymer Science 7 (1963), S. 873-885 
    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 treatment of butyl rubber containing carbon black can considerably reduce “structure effects” in the dynamic properties of the vulcanizate, although swelling measurements indicate that G ∞ the shear modulus at very high amplitudes is unaltered. This paper compares the G′, G″ and phase angle δ changes that occur with the amplitude of oscillation for both a normal butyl rubber containing HAF black and a vulcanizate of the same composition but which has been subjected to an additional heat-treatment process with N-methyl-N, 4-dinitrosoanaline.
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  • 135
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    Journal of Applied Polymer Science 7 (1963), S. 861-871 
    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: A theory is developed to account for the restricted swelling in solvents of crosslinked elastomers containing reinforcing fillers. Assuming swelling to be completely restricted at the filler-rubber interface due to adhesion, the following relation is obtained: \documentclass{article}\pagestyle{empty}\begin{document}$$ v_{ro} {\rm /}v_r {\rm } = {\rm 1} - [3c(1 - v_{ro} {}^{1/3}){\rm } + {\rm }v_{ro} - 1]\phi /(1 - \phi ), $$\end{document} where vr is the volume fraction of rubber in the swollen rubber phase, Vro is the same quantity referred to on otherwise analogous, unfilled vulcanizate, Φ is the volume fraction of filler, and c a parameter depending on the filler, but independent of Φ and Vro. This equation is shown to hold for a large volume of experimental data on carbon blacks, involving four rubbers, several sulfur vulcanizing systems, five solvents, and a wide range of crosslinking. Conformance with the theory indicates that carbon blacks are firmly bonded to the rubber and that, in the sulfur crosslinking systems investigated, they have no significant effect on the stoichiometry of vulcanization (although they may affect the rate of vulcanization). Illustrative examples of applications of the theory to problems in filler reinforcement and vulcanization are shown.
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  • 136
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    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: Eight esters of 7-aminoheptanoic acid were prepared as monomers for nylon 7 (polyheptanamide). They were made from ε-caprolactone via the route; 6-chlorohexanoic acid, alkyl-6-chlorohexanoate, alkyl-6-cyanohexanoate, alkyl-7-aminoheptanoate. The stability of these esters against polymer formation during distillation and at room temperature increased with the number of C atoms in the alcohol. When the esters were heated at 270°C. to form the polyamide, the same trend in stability was observed; the polyamides obtained were of too low molecular weight for melt spinning. Upon heating ethyl-7-aminoheptanoate with water (mole ratio 1 to 〉 3) at 100°C., a mixture of 7-aminoheptanoic acid with mainly dimeric acid and ester was obtained. This product (“precursor”) was a stable solid at room temperature which could readily be converted at atmospheric pressure within 2 hr. to high molecular weight, spinning grade nylon 7. The melting point, density, moisture regain, and sticking temperature of nylon 7 were compared with those of nylons 6, 8, 9, 10 and 11. Nylon 7 was melt spun into high tenacity yarn and its textile properties were discussed in comparison with those of nylons 6 and 66. The low oligomer content of nylon 7 (1.5%) made extraction of the resin before spinning unnecessary.
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  • 137
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    Journal of Applied Polymer Science 7 (1963), S. 897-908 
    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: Ring-substituted styrenes were prepared and polymerized. They usually had higher glass transition temperatures than polystyrene. In some disubstituted systems the Tg was an additive function of the individual groups. Crystallinities of methyl-substituted polymers varied, depending upon the ring positions involved. Crazing tendencies were equivalent to those in polystyrene.
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  • 138
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    Journal of Applied Polymer Science 7 (1963), S. 923-933 
    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: Sheets of isotactic polypropylene were prepared to have initially random orientation and were subsequently rolled at temperatures below the crystalline melting point. Their crystal orientation was investigated. The orientation of the c axis (fiber axis) was determined from pole figure data obtained by x-ray diffraction. It was found that rolling produced orientation of the c axis in two preferred directions in the plane defined by the rolling direction and the normal to the sheet. These two directions made equal angles of inclination with the rolling direction. With increased severity of rolling the component of the orientation vector in the rolling direction increased and the angles between the preferred c axis orientation and the rolling direction decreased. Increasing the temperature reduced the angle of inclination of the preferred c axis orientation. This double c axis orientation was not observed in extruded film. An explanation of the c axis orientation in cold-rolled polypropylene is offered on the basis of local necking down within the sample during the deformation.
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  • 139
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    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: Flow behavior of ten copolymer solutions of polyacrylonitrile and polymethyl methacrylate in concentrations up to 16% was studied at 30°C. with the use of capillaries of constant diameter but different lengths. The shear rate and shear stress range covered were up to 200,000 sec.-1 and 800,000 dynes/cm.2, respectively. A rheological model of the form log D = A0 + A1 (log τ)β + A11 (log τ)2β was employed in determining the inflection point of the flow curve by computer analysis. A marked dependence of the flow curve upon the lenght-to-diameter ratio was observed when l/d ratio decreased to below 300. At shear rates above 50,000 sec.-1 the capillary “end effect” corrections and the kinetic energy corrections were found to be large for the concentrated and dilute solutions, respectively. The flow curves were characterized in terms of the inflection point in accordance with the treatment of Schurz. An upper Newtonian viscosity η* was observed at shear rates above 150,000 sec.-1. Up to a concentration of about 1%, the value of the upper Newtonian viscosity was such that the calculated ηsp/C was essentially independent of C and equal to [η*] obtained by extrapolation to infinite dilution. The values of the heat of activation for viscous flow were found to be dependent upon the applied shear stress.
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  • 140
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    Journal of Applied Polymer Science 7 (1963), S. 947-957 
    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 shape of the cells in a foam is thought to be determined by the interplay between viscosity and surface tension. In order to assess the relative importance of the two, a simplified model is set up which considers only surface tension. It is assumed that the cells are of uniform cross section in one direction and are based on a regular hexagonal lattice in the other two. The resulting two-dimensional problem is solved by means of the calculus of variations. For high density foams the voids take the form of circles centered within each hexagonal cell. For low densities (below about 9% solids) the solid part is concentrated at the vertices, between tangential circular areas, connected by straight segments of zero thickness. This illustrates the importance of viscosity, since in real foams the cell walls will break if too thin, while the thinner the walls become, the greater is the effect of viscosity in opposing further thinning.
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  • 141
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    Journal of Applied Polymer Science 7 (1963), S. 959-969 
    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 initial stages of isotactic polypropylene oxidation were investigated by oxidizing at 130°C. to various extents up to 10 ml. of oxygen consumed per gram of polymer. The development of infrared absorption bands in the carbonyl regions was followed, as increasing amounts of oxidation occurred. The oxidation uptake curves showed that both autocatalytic rate and induction time depended primarily on the thickness of the sample, contrary to the case of polyethylene. This indicated the initiation process was primarily diffusion controlled for samples of the thickness range studied. The presence of copper shortened the induction times and increased the autocatalytic rate. In this case, the dependency of the induction time on thickness was less. Dielectric data showed that polypropylene became unsuitable electrically at about the point where the autocatalytic oxidation set in. It was also found that the effects of prior exposure to oxidative conditions were cumulative to a considerable extent, and thus resulted in shorter induction times.
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  • 142
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    Journal of Applied Polymer Science 7 (1963), S. 935-946 
    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: Recent experimental and theoretical work on the concentration-dependent diffusion of solvents in polymers has led to a reasonably detailed understanding of the processes involved. The possibility exists of supplementing standard but costly surveillance testing with rapid laboratory-scale measurements of plasticizer migration. Many solvent-polymer systems conform rather closely to the assumption that the amount of material transferred by diffusion is a function of the composite variable t1/2/l. This means that any scale factor applied to the diffusion path length, in a one-dimensional system, may be compensated for by applying the square of this factor to the time. It has been shown that this assumption can apply with reasonable accuracy to plasticizer diffusion in the propellant-inhibitor systems. By approximating a particular 2 in. rocket charge with a one-dimensional model, it is possible to predict the time required for the unit's inhibitor to reach specified levels of plasticizer migration at any storage temperature of interest. A large temperature coefficient appears to be associated with the equilibrium plasticizer migration in the system chosen for experiment, as well as with the rate. Unless suitable allowance is made, this can lead to serious misinterpretation of the results of the surveillance that has been accelerated by raising the storage temperature.
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  • 143
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    Journal of Applied Polymer Science 7 (1963), S. 971-992 
    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 complex elastic modulus G*(ω) = iG′(ω) + iG′(ω) is shown to be a function not only of the frequency (ω) but also of the damping factor a if the strain is of the form x = x0 exp {- at} sin ωt. The general equations for G*(ω,a) = G′(ω,a) + iG″ (ω,a) = are derived in terms of the relaxation spectrum. The use of a spring to aid the specimen and reduce the ratio a/ω is discussed, and its desirability demonstrated. If data are thus available in terms of either G″(ω) or G″(ω,a) the iterated second approximation of Ninomiya and Ferry provides a rapid and powerful method of finding the relaxation spectrum. To the accuracy to which the time-temperature reduction factor aT is known or can be predicted by means such, for example, as the WLF equation, the function G″(ω,a) over a temperature range at nearly constant frequency can be translated into terms of G″(ω,a) at constant temperature and varying frequency. In such cases, the relatively simple torsional pendulum, or some analogue of it, can economically provide a characterization of the viscoelastic behavior of the material over an extended time or frequency range.
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  • 144
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    Journal of Applied Polymer Science 7 (1963), S. 1003-1013 
    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: Replica electron microscopy has been used to elucidate the physical mechanisms by which various additives afford ozone resistance to natural rubber. There exist two classes of chemical antiozonants, namely, those that enhance the critical energy required for ozone cracking and those that retard the rate of crack growth; representatives of these two classes were used in the investigation. The process involved in the first of these protective mechanisms was found to be the formation at the exposed surface of an inextensible layer some 100 A. thick and inert to further ozone attack. That giving rise to rate retardation also involved the formation of a surface layer, but the layer was susceptible to further ozonolysis and, eventually, complete degradation.
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  • 145
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    Journal of Applied Polymer Science 7 (1963), S. 1015-1022 
    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 steady-state (d.c.) electrical conductivity of polypropylene has been measured as a function of temperature (25-150°C.) and field strength (0-94 kv./cm.). The temperature coefficient of the conductivity is 34.6 kcal./mole expressed as an activation energy. This is much larger than the activation energy for diffusion of small molecules in the same polymer. Thus, ionization rather than diffusion appears to be the primary activation process. The conductivity is nonohmic; the conductance quotient is a linear function of field strength but is larger than predicted by Onsager's theory. The ion “jump distance” as evaluated from the isothermal field dependence, is the same order of magnitude as the diffusional mean free path estimated from diffusion studies in other polymers. The conductivity, conduction activation energy, and field dependence appear to be relatively insensitive to polymer crystallinity.
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  • 146
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    Journal of Applied Polymer Science 7 (1963), S. 1023-1030 
    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: Sol-gel analysis, that is, the measurement of the fraction of rubber remaining unconnected to the network as a function of the degree of cure, has been used to estimate the extent of chain scission in the vulcanization of natural rubber with dicumyl peroxide at 130°C. For peroxide concentrations in the range 1-5% and masticated rubbers of M̄n = 0.84-2.67 × 105 there are only 1-3 sites of scission per 100 crosslinked isoprene units.
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  • 147
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    Journal of Applied Polymer Science 7 (1963), S. 1425-1438 
    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: Accurate measurement of several types of fatigue failure in polymers was obtained with a flexing machine equipped with an automatic camera. The technique is described at length. Observations made include that an antiozonant interferes with crack initiation, that a crack may well start under the surface, and that in the growth of a crack the elastic force is equivalent to the hysteretic force. Several photographs show aspects of crack initiation.
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  • 148
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    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: As a phase of an investigation of the cellulose-epoxide reactions, experiments have been performed in which epichlorohydrin reacted with cotton cellulose in the presence of sodium hydroxide and various salts. Acidic and basic salts, as well as those which are relatively neutral in aqueous solutions, were used in pretreatments for the cellulose-epichlorohydrin reaction. No reaction with cellulose occurred in the presence of acid salts and only very slow addition of epichlorohydrin to cellulose in the presence of neutral salts; the greatest reaction was produced with basic salts. Particular emphasis was given to use of certain salts known to cause epichlorohydrin to undergo a type of cyclization reaction. Previously published methods, used for imparting both wet and dry crease resistance to cotton fabrics by means of diepoxides in the presence of NaOH, have resulted in wet crease resistance only when applied to the application of epichlorohydrin. Among the basic salts investigated, 20% solutions of sodium azide used in pretreatments were found to produce low weight gains of epichlorohydrin and a fair degree of dry and wet crease resistance in cotton after a slow reaction at 25°C. or a faster reaction at 80°C. The greatest improvement in dry crease resistance with epichlorohydrin was obtained by pretreatments with concentrated solutions of sodium orthosilicate, sodium metasilicate, or trisodium phosphate at 80°C. The effects of amount of water at time of reaction as well as speeds of reaction with the various pretreatments have been considered. Optical and electron microscopical examinations of fibers and ultrathin cross sections of fibers, respectively, after immersion in cupriethylene diamine (cuene) have indicated that the cellulose-epichlorohydrin reaction at 80°C. after pretreatment with concentrated solutions of silicates or phosphates differed from that after pretreatment with sodium hydroxide at all concentrations. Even when the pretreatments were with dilute sodium hydroxide, the epichlorohydrin-reacted fibers were more swollen in cuene than were those treated fibers which had been pretreated with the concentrated silicates or trisodium phosphate solutions. Decrease in amount of swelling and dissolution in cuene was found to correlate with increase in dry crease resistance of the fabrics. While all these treated fabrics possessed high wet crease resistance, only those pretreated with the aforementioned concentrated salt solutions possessed good dry crease resistance. Effects of base-catalyzed addition of certain monoepoxides to cotton on the resultant crease resistance properties of the fabrics have been reported and compared with properties imparted by epichlorohydrin. Attempts have been made to explain why the number of cellulose crosslinks formed per unit of time by epichlorohydrin is greater, when silicates or phosphates at high concentrations are present with hydroxyl ions, than when hydroxyl ions only are present.
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    Journal of Applied Polymer Science 7 (1963), S. 1451-1469 
    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: Allyl glycidyl ether and maleic anhydride, mixed in equimolar quantities, cure together readily in the presence of air, peroxide, and/or Lewis acids. Outstanding properties of the castings formed are hardness (Barcol 50-60 at 25°C., 30 at 150°C.), clarity and heat distortion temperature (165-168°C.). Color is yellow to amber, and strength properties are adequate. Water resistance is fair. The mixture is too thin for convenient use in laminating, but it can be bodied by heating (1 hr., 110°C.), giving a syrup of 50 cpoise. In glass cloth laminates, through-cure appears to be inhibited by the glass. The addition of styrene overcomes this effect. Small amounts are best (5-20%), since large quantities impair elevated temperature strength. Unusually good strength is attained even at 500°F., but resistance to aging at 500°F. is poor.
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  • 150
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    Journal of Applied Polymer Science 7 (1963), S. 1471-1485 
    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: Moldings were irradiated at ambient temperature in vacuo with 2 m.e.v. electrons to doses of 5.9-7.3 Mrad. The decay of radicals was followed by EPR spectroscopy at 80, 55, and 30°C. while simultaneous extinction measurements were made at 300-700 mμ with a recording spectrophotometer. The radical decay data indicated the presence of three species at each temperature, decaying exponentially with time, with half-lives of 20 min., 210 min., and 135 hrs. at 80°C. of 40 min., 400 min., and 141 hrs. at 55°C., and of 54 min., 720 min., and 3200 hrs. at 30°C. G values of 1.6, 2.0, and 1.4 were obtained for radical formation at 25°C. by back-extrapolation of decay curves from the three temperatures to the end of the irradiation period. The activation energy of radical decay was found to be 4.4, 5.0, and 13.7 kcal./mole for the short-lived, intermediatelived, and long-lived radicals, respectively. The optical data has a broad absorption maximum at 500-550 mμ and a series of seven absorption peaks with maxima at 505-510, 483-485, 458-460, 430-435, 400-405, 364-365, and 329-330 mμ. The concentration of the material producing the broad bands was found to be inversely proportional to the long-lived radical concentration. The fine-structure peaks are consistent with literature data for a polyene chain of 16-17 conjugated double bonds.
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  • 151
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    Notes: We have measured the solubility of mixtures of polybutadiene and polystyrene in toluene, benzene, and carbon tetrachloride, using polymers of various molecular weights and mixed in various proportions. The equations developed by Maron for solutions of nonelectrolytes have been modified for three components and for solutions of low molecular weight polymers at high concentrations. The application of these equations has provided estimates of the polymer-polymer interaction parameters χ23. The polymer-solvent interaction parameters χ12 and χ13 apparently are functions of the concentration and are not readily obtained from the present limited data.
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  • 152
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    Journal of Applied Polymer Science 7 (1963), S. 1509-1513 
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    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: A process for one-step polyallylation of phenols was developed. Phenol is polyallylated in xylene in the presence of 3 moles of finely divided sodium hydroxide. Three moles of allyl chloride are added at such a rate as to maintain the reflux temperature at 110 to 120°C. Water is continuously azeotropically removed. The product contains allyl ethers of mono-, di-, and triallyl phenol. The bulk of the material is allyl ether of dially phenol which can be subjected to Claisen rearrangement followed by glycidyl ether formation and epoxidation of the glycidyl ether of triallyl phenol.
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  • 153
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    Journal of Applied Polymer Science 7 (1963), S. 1515-1521 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Methacrylylacetylacetone and acrylylacetylacetone were prepared by acylation of acetylacetone enolate salts with methacrylyl chloride and acrylyl chloride, respectively. Both monomers yielded poor homopolymers. Methacrylylacetylacetone formed copolymers with styrene and methyl methacrylate without difficulty.
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  • 154
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    Journal of Applied Polymer Science 7 (1963), S. 1523-1529 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Monomethacrylyldimethylglyoxime and dimethacrylyldimethylglyoxime were prepared by acylation of dimethylglyoxime with methacrylyl chloride. Monoallyldimethylglyoxime and diglycidyldimethylglyoxime were prepared by alkylation of dimethylglyoxime sodium salt with allyl bromide and epichlorohydrin, respectively. The monomethacrylyl derivative formed a copolymer with methyl methacrylate and the dimethacrylyl derivative yielded a homopolymer. Nickel chelates could be formed from both polymers. Diglycidyldimethylglyoxime was easily copolymerized with a number of diamines. A polymer formed as a by-product from the preparation of the diglycidyldioxime was easily cured with m-phenylenediamine.
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  • 155
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    Journal of Applied Polymer Science 7 (1963), S. 1543-1547 
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    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 oxidative stress relaxation of peroxide vulcanizates of various grades of natural rubber has been investigated at 100°C. The rubbers were examined both with and without hot acetone extraction before or after cure. Highly purified rubber vulcanizates exhibited autocatalytic relaxation, but those based on crêpe or smoked sheet did not, because they retained natural antioxidant even after extraction. Autocatalysis was no longer found in extracted purified rubber vulcanizates if these were prepared from a mix containing phenyl-β-naphthylamine. The presence of such an antioxidant reduced network scission but had less effect upon the amount of crosslinking taking place during aging.
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  • 156
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    Keywords: Chemistry ; Polymer and Materials Science
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    Notes: Thermal properties and resistance to crazing of copolymers and terpolymers of 2,5-dichlorostyrene and 3,4-dichlorostyrene have been studied. Copolymers based on 2,5-dichlorostyrene showed little or no improvement over polystyrene in craze resistance or glass transition temperature. Although copolymers of 3,4-dichlorostyrene were generally brittle and crazed readily, poly(3,4-dichlorostyrene-co-2-ethylhexyl methacrylate) and poly(3,4-dichlorostyrene-co-n-hexyl methacrylate) crazed less readily than polystyrene.
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  • 157
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    Journal of Applied Polymer Science 7 (1963), S. 1549-1556 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Water and salt fluxes through synthetic membranes were measured as functions of pressure. In the pressure range 0-60 atm. both the water permeation rate constant and the salt permeation rate constant were independent of pressure. The water flux increased linearly with pressure driving force (hydraulic-osmotic). The changes in salt flux were small. These changes were proportional to changes in the activity of the salt solutions due to concentration and pressure effects. Good agreement was obtained between the experimental flux data and the kinetic equations describing the process.
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  • 158
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    Journal of Applied Polymer Science 7 (1963), S. S27 
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    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
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  • 159
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    Journal of Applied Polymer Science 7 (1963), S. S33 
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    Keywords: Chemistry ; Polymer and Materials Science
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  • 160
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    Notes: The mathematical theory of periodate oxidation of unfractionated starches was studied. The degrees of polymerization (DP) of the amylose and amylopectin components of the starch were considered to be unknown, whereas the proportion of amylose in the starch, the repeating chain length of the amylopectin component, and the amount of formic acid evolved on quantitative oxidation were considered to be experimentally ascertainable and thus known. The treatment thus reduces to an approximate solution of one equation with two unknowns. It is shown that certain inequalities are then valid, when the following information can be obtained: (1) the upper and lower DP limits of each component, (2) the extent of degradation of a randomly degraded starch, and (3) the maximum relative errors involved in the determination of the DPs of the components by the periodate method. A numerical example is given to show the application of the method in laboratory practice.
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  • 161
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    Journal of Applied Polymer Science 7 (1963), S. 643-665 
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    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 purpose of this analysis is to find a method of calculating the maximum stress at failure from the variation of the peel force with the thickness of the adhesive layer If the failure is in the binder/substrate interface, this maximum stress is the adhesive bond strength. In the model it is assumed that, among other things, both substrate and adhesive are Hookean, the stresses parallel to the symmetry axis of the sample and the shear stresses are negligible, and the deflection of the substrate prior to failure is small. The latter assumptions are very questionable but the assumption involving Hookean behavior is a good approximation. It is shown that the rate of deformation in the sample is in the 104 to 106%/min. range. At such high rates of deformation viscoelastic bodies are expected to approach Hookean behavior. Two separate equations are derived describing the variation of the peeling force with adhesive layer thickness. These equations also contain an additional variable, the slope angle of the substrate at the failure point. This variable can be eliminated by combining the two equations. The parameters in the final expressions are the moduli of the binder and substrate, thickness of the binder, width of the sample, and the maximum stress at the failure point. The theoretical analysis also defines the geometry of the sample and allows the estimation of the rate of strain in the adhesive and in the substrate. Furthermore, it predicts the existence of compressive stresses which develop prior to tensional stresses. These compressive and tensional stresses in the sample can be separately calculated, and it is possible to establish the size of the area where these stresses exist at steady state conditions. The measured peeling force is proportional to the difference between the sum of tensional and the sum of compressive stresses. Data obtained with cellophane substrates and acrylic binders at high peeling rates, where the force is rate independent and the failure is adhesive, are analyzed in terms of the theory. The rheological parameters calculated from peel test data are of the right order of magnitude and the shape of force/adhesive layer thickness plot is consistent with theoretical predictions. It is also shown that the magnitude of the compressive force in the glue line changes only to a small extent with the thickness of the adhesive layer and that the tensional force in the glue line is approximately proportional to the area under tension.
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  • 162
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    Journal of Applied Polymer Science 7 (1963), S. 685-694 
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    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: An analysis of the parameters involved in torsional braid measurements is given. It is found that the amount of polymer on the braid controls the level of rigidity modulus attained by the composite specimen, but does not affect the measured glass transition temperature of the polymer. Treating the torsional braid system as a fabric braid filled polymer system, an empirical relation is given relating the measured modulus, G, to the modulus of the unfilled polymer, G0, and the volume fractions of voids, ϕv and support ϕs. This equation takes the form, \documentclass{article}\pagestyle{empty}\begin{document}$$ G/G_0 {\rm } = {\rm [1 } + {\rm (}k_s \phi _s {\rm } + {\rm }k_v \phi _v )]/[1 - (S_s ^\prime \phi _s + S_v ^\prime \phi _v )]^2 $$\end{document} where ks, kv, Ss′, and Sv′ are constants. This equation is evaluated for the polystyrene-cotton thread system. The effect of braid length on the measured modulus is discussed.
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    Journal of Applied Polymer Science 7 (1963), S. 695-701 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Polyethylene films were irradiated in various atmospheres by gamma-rays from a Co60 source, and solubility measurements against xylene were carried out at 80°C. In NO2 and O2, the crosslinking of polyethylene is depressed markedly but in NH3, Cl2, and SO2 not so much. On the other hand, N2O accelerates the crosslinking appreciably. In CO and H2, neither the depressive nor the accelerating effect is observed within a limit of error. In O2, the depressive effect is more considerable at higher gas pressure and at lower dose rate; however, in N2O the accelerating effect is reduced at higher gas pressure, and shows dose-rate independence within the range of our experiments.
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  • 164
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    Notes: The study of the interchange reaction of thiols with disulfides is extended to include additional thiols and conditions for redistribution. In aqueous suspension, polymeric disulfides are reduced in molecular weight to widely different extents by thiols of varying structures. Water-soluble thiols as mercaptoethanol, and tertiary thiols as t-butyl mercaptan, are relatively ineffective in cleaving. The presence of sodium disulfide with some of the thiols, particularly the thiophenols and 2-mercaptobenzothiazole, retarded cleavage by the thiols. A study of the molecular weight of the polymer as the cleavage by thiols proceeded indicated that short chain lengths were gradually removed from the surface of the polymeric particles. The partial cleavage of a disulfide polymer by a mixture of sodium sulfite and sodium hydrosulfite produces a disulfide polymer of lower molecular weight and terminal thiol groups. This product should be capable of self-redistribution to a random distribution. The liquid polymer resulting from the cleavage had a high heterogeneity index (M̄w/M̄n). Efforts to randomize in bulk to the theoretical index of 2.0 by heat, ultraviolet light, water, and amines were not successful. It was found possible to effect the reaction of the disulfide polymer with butyl mercaptan in solution in dioxane with sodium phenolate as catalyst. The conclusion is drawn that the reaction of a thiol with a disulfide, both in aqueous suspension and in dioxane, is ionic rather than radical.
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  • 165
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    Journal of Applied Polymer Science 7 (1963), S. 1093-1116 
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    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: A method is described for evaluating flexural fatigue properties of unsaturated polyesters. With the use of the Sonntag fatigue machine and a modified version of the Prot principle, dynamic parameters and fatigue properties can be readily determined. Testing of castings with no reinforcement reveals two different modes of resin fracture, brittle and plastic. A plastic fracture implies that the resin yields before breaking. Reproducibility of the results is directly related to the type of fracture, ranging from very good for a plastic resin to very poor for a brittle. Close proximity of yield points and endurance limits for plastic resins confirms validity of Prot's method of extrapolating the latter parameter. Incorporation of two layers of glass cloth in positions corresponding to the outermost plies in a laminate shows that failure at the glass-resin interface may be the overriding cause of laminate breakdown. Both plastic and brittle resins become stiffer in the presence of glass, but only the plastic resin is realizing its inherent strength to give a stronger reinforced casting. The brittle resin is, on the other hand, weaker with glass present because of inability to dissipate local stress concentrations at the warpfilling crossovers. The break amplitude is a particularly significant parameter because it is expected to be the same in a normal laminate as in these castings with only the outermost plies present. Additional plies would merely increase stiffness and, correspondingly, the stress to reach amplitude coincident with failure at the outermost plies. Use of relatively thick test bars (0.5 in.) permits insertion of a thermocouple in the neutral plane without affecting dynamic properties. Measurement of the temperature rise during flexing allows assessment of the damping capacity of the glass-resin system, which is of particular importance for resonance fatigue. By this means, three different types of glass-resin systems could be distinguished: (1) weak and high damping (plastic), (2) strong and low damping (brittle), (3) strong and high damping (tough). For a particular resin, the behavior is determined by the basic composition as well as by degree of cure. For well-cured polyester samples, several links were found between dynamic parameters, such as stiffness, fatigue strength and damping, and basic composition. Distance between crosslinks in the polyester backbone thus appears to have a direct bearing on strength and damping. Such relationships are valuable in that they make possible predictions of the fatigue behavior of a given polyester formulation.
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    Journal of Applied Polymer Science 7 (1963), S. 1133-1145 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Silicon containing chain and ring formals of the structures were synthesized from the reaction of a chlorosilane with formaldehyde or a formaldehyde donor in acid solution or in the presence of an HCl acceptor. Mono-, di-, tri-, and tetrafunctional “silyl formals” were obtained; they are oily products of various degrees of polymerization and of relatively high refractive index and specific gravity. Silyl formals are stable at room temperature. They are useful intermediates in cases in which a siloxy group should be introduced into an organic molecule by reaction with an organic OH group or active hydrogen. Tri- and tetrafunctional silyl formals are effective crosslinkers in various systems.
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    Journal of Applied Polymer Science 7 (1963), S. 1147-1152 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The effect of antioxidant on the crosslinking reaction occurring during the oxidation of sulphur vulcanizates of natural rubber was investigated by using both continuous and intermittent stress relaxation measurements. Similarly, by means of continuous stress relaxation and equilibrium swelling measurements the crosslinking reaction in vacuum was followed. The presence of antioxidant or removal of air reduced considerably both continuous and intermittent relaxation and also the difference between them, which measures the crosslinking. The crosslink formation must therefore form part of the sequence of oxidative reactions.
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    Journal of Applied Polymer Science 7 (1963), S. 1815-1832 
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    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 dynamic modulus and loss angle of butyl vulcanizates containing both normal and attrited carbon black (HAF) have been studied over a wide strain amplitude range. Large changes are observed in the modulus with the attrition of the black. Hot milling treatment accentuates these changes. The decrease of modulus with the logarithm of the strainwork is shown to be sigmoidal in form. When the modulus is normalized between, G0, the shear modulus at very low strains and, G∞, the shear modulus at high strains, the resulting plots with respect to strainwork are independent of the concentration of the black and the condition of the vulcanizate.
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  • 169
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    Journal of Applied Polymer Science 7 (1963), S. 1833-1852 
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    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: Microinterferometry was applied as a quantitative method for determining the transversal distribution of graft concentration instead of the usual determination of an overall graft concentration of the radiation-induced polypropylene-styrene graft copolymer. Since polystyrene has a higher refractive index than polypropylene, the features of the interference fringe provide direct visualization of the distribution curve of graft concentration. The application of the method leads to clarify the effects of radiation dose rate, film thickness, monomer concentration, temperature, and grafting technique on the graft composition. A retardative effect on grafting appears in the vicinity of the surface, when the grafting is performed in lower radiation field and with thinner film. This is well explained by the variation in the grafting rate constant as a function of monomer concentration in the film. Furthermore, the post-irradiation effect and accelerative effect of methanol were followed. They act effectively to form the surface, volumetric, and embedded grafts. The method has also proved useful in routine examination for a qualitative estimate of the graft copolymer.
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    Journal of Applied Polymer Science 7 (1963), S. 1853-1866 
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    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: New vinyl oil monomers have been prepared by combining epoxidized unsaturated oils with vinyl carboxylic acids. This is accomplished by heating the reactants in the presence of free radical inhibitors and appropriate reaction catalysts. The reaction consists of cleavage of the oxirane ring followed by addition of the vinyl acid through its carboxylic group. By varying the reactants and the conditions of reaction, a large family of related, but different, vinyl oil monomers can be prepared. Vicinal methacryloxy-hydroxy soy oil monomers are clear, yellow, medium viscosity (2000-2500 cpoise), high molecular weight (1300-1500) liquids. Chemical analyses are presented for typical preparations. The monomers readily homopolymerize by a free radical mechanism to clear, solid, thermoset resins. They are compatible with a variety of commercial vinyl monomers and form copolymers which range from highly viscous liquids through soft gels, to tough rubbery products and hard resins. Data are presented on physical properties of copolymer castings of several specific vicinal methacryloxy-hydroxy soy oil monomers.
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    Journal of Applied Polymer Science 7 (1963), S. 375-382 
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    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: An investigation of the insolubles found in viscose solutions and various microscopic techniques are described. The emphasis is placed on substances which apparently originate from the pulp starting materials. Viscose insolubles may be subdivided into four broad groups: swollen fiber fragments, granular dispersion, submicroscopic particles, and miscellaneous particles. The electron microscope and polarizing microscope reveals characteristic differences between the swollen fiber fragments from sulfate pine pulps and those from the sulfite. Comparison with the original pulp fibers shows that these fragments contain primarily the more resistant parts of the fiber wall; the resistant layers are principally the S1 and the S3 layers and also a fraction of the S2. Light and electron microscope studies indicate that the granular dispersions comprise different heterogeneous materials; fiber debris, lignin residues, and inorganic materials appear to be the main constituents in this group. Silica particles, originating as cell inclusions, and some dirt particles are the only miscellaneous materials traceable to the pulps; the others originate as contaminants from the viscose process and equipment.
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    Journal of Applied Polymer Science 7 (1963), S. 1613-1628 
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    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 result of a phenomenological study in the analysis of uniaxial and biaxial tensile behavior of a variety of filled systems is described. A correlation is given that appears to serve as a tensile failure criterion for most of the systems investigated. The storedenergy function W, assumed to be equal to the area under the stress-strain curve, has been found to obey the relation W = A(1 - exp {-B(Q - 3)}), where A and B are constants and Q is related to the first or second strain invariant. In general, the total stored energy up to break, divided by A, has a value between 0.7 and 0.8, which appears to be independent of strain rate and temperature. This constancy has also been verified by an independent set of data.
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    Journal of Applied Polymer Science 7 (1963), S. 1597-1611 
    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: A study of the thermal diffusivity of polymer melts as a function of temperature over the range 25-325°C. is described. Measurements were carried out with an apparatus especially designed and constructed for this purpose; this apparatus and the theoretical treatment of data obtained with it are treated in detail. The polymers examined include polystyrene, poly(methyl methacrylate), some of their copolymers, poly(vinyl chloride), linear polyethylene, polyacetal, polycarbonate, cellulose-acetate-butyrate, some “highimpact” polymer blends and terpolymers, and some higher methacrylates. The thermal diffusivities of the melts vary from about 11 × 10-4 cm.2/sec. (for linear polyethylene) to about 5 × 10-4 cm.2/sec. (for poly(sec-butyl methacrylate)). In general the thermal conductivity of an amorphous polymer decreases as it passes from the glassy state to a melt, but remains quite constant over a wide temperature range in the melt state. On the basis of a limited amount of data one might tentatively conclude that the thermal diffusivities of the melts of vinyl polymers become lower as larger as longer groups are added to the carbon-carbon backbone. As regards molecular weights equal to those common for molding powders, molecular weight seems to have no effect on the thermal diffusivity.
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  • 174
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    Journal of Applied Polymer Science 7 (1963), S. 273-279 
    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: Derivatives of poly(vinyl alcohol), styrene-maleic acid copolymer, cellulose, and gelatin have been made which incorporate aromatic azide groups into the polymer molecule. The relative rates at which these polymers become crosslinked on exposure to ultraviolet light were measured. A preliminary discussion is given of the structural factors involved in the photolytic decomposition and subsequent coupling reaction.
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  • 175
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    Notes: Resins were prepared from the respective monoepoxystearoyl and diepoxystearoyl esters of the isomeric dihydroxybenzenes and phthalic anhydride. The average value of the heat distortion temperature of the resins derived from the monoepoxystearoyl esters was 17°C. and that from the diepoxystearoyl esters was 121°C. From results of previous work, it was concluded that the effect of substitution of dioxyphenylene for dioxyethylene was to increase the heat distortion temperature 42-46°C.
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  • 176
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    Journal of Applied Polymer Science 7 (1963), S. 493-506 
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    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 individual contributions to the observed normal tensile stress in capillary jets of Newtonian and viscoelastic liquids, measured by means of expansion-contraction experiments described in earlier publications of the authors, is discussed. The surface tension contribution is calculated. The contribution from the relaxing velocity profile is determined empirically for the Newtonian jet; it is estimated for the viscoelastic jet. The internal normal stress, developed in the capillary, and the external normal stress, developed beyond the capillary nozzle exit, are described, but not in a quantitative manner. Because of the complexity of the equations describing the viscoelastic jet, these stresses are not yet able to be separated in the general case. At high ejection velocities, however, the profile relaxation and the external normal stress should be smaller than the internal normal stress if the liquid is highly viscoelastic. One should, however, be fully aware of the approximate nature of the results when expansion-contraction experiments are used to obtain a measure of the normal stress developed during flow in a capillary. Such experiments, unfortunately, are not as useful as one would like them to be.
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  • 177
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    Journal of Applied Polymer Science 7 (1963), S. 507-514 
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    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 intrinsic viscosity-molecular weight relationship has been determined for synthetic cis-1,4-polyisoprene prepared with butyllithium initiator. The best representation of our results is the equation, [η] = 2.00 × 10-4 (M̄v)0.728, for intrinsic viscosities determined in toluene at 30°C. This relationship agrees, within experimental error, with that obtained for natural rubber by Carter, Scott, and Magat.
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  • 178
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    Journal of Applied Polymer Science 7 (1963), S. 533-544 
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    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: When liquids are sorbed by wool or other textile fibers it is necessary to distinguish between sorbed liquid and liquid held mechanically on the surface and in the interstices between fibers. A method is described by which the latter can be removed by washing the fibers under anhydrous conditions with liquid propane at -78°C. The propane is subsequently distilled off at room temperature leaving the sample of wool containing sorbate. Small corrections are made for loss of sorbate during washing and distillation. The method is accurate to about ±2%. Sorption curves and saturation values are recorded for ethanol, n-propanol, isopropanol, acetone, and n-butanol and initial rates of sorption for n-pentanol, n-hexanol, n-pentane, and benzene. A theory is proposed in which it is postulated that holes of various sizes can be produced by thermal fluctuations and also interactions with the sorbate. A consequence of the theory is that even large molecules can penetrate the fiber if given sufficient time. The experimental values of the initial rate of sorption are interpreted in terms of the volume, shape and ability to form hydrogen bonds of the sorbate molecule. The rate of sorption is very sensitive to quite small modification of the wool fiber. The volume sorption at saturation is found to be constant for water, methanol, ethanol, n-propanol, isopropanol, and n-butanol with a mean value of 34.1 ± 0.7 cm.3/100g.
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  • 179
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    Journal of Applied Polymer Science 7 (1963), S. 515-531 
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    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: By means of a constant stress test, the environmental stress-cracking behavior of linear polyethylene has been studied on a macro and micro scale in an effort to determine the mechanism of the process. Upon the application of stress, linear polyethylene develops a network of very fine, elliptical fissures, the edges of which are connected by cold-drawn material. In the absence of an active environment, these fissures slowly grow and interconnect, resulting ultimately in the formation of a “neck.” When exposed to an active environment, however, the cold-drawn material ruptures as it is formed at the tips of the fissures. Unsupported, these fissures grow rapidly and interconnect resulting in sample failure. Fissures form both around and through the centers of spherulites with less cold drawing occurring at the interspherulite boundaries. Macroscopic studies confirmed the observation that active environments attack stressed polyethylene specifically at microzones of cold drawing. The effect of low molecular weight hydrocarbon species on the stress-crack resistance of linear polyethylene was evaluated. The role of flaws in the process is also discussed. Attempts have been made to establish a criterion of environmental activity. All of the active stress-cracking agents studied were found to reach similar levels of absorption in polyethylene; however, the specific chemical nature of the environment and not merely its level of absorption determines its ability to cause stress cracking.
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  • 180
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    Journal of Applied Polymer Science 7 (1963), S. 545-555 
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    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 partial specific volume of wool in water and various organic liquids is determined pyconometrically over the whole range of concentrations during absorption and desorption. Sorption of water in the range 0-2.5% by weight occurs with a constant volume contraction amounting to 36% of the volume of the liquid sorbed. This is due largely to electrostriction of water molecules sorbed on charged groups in the wool. Ethanol sorbed by wool undergoes a rearrangement within the fiber which increases considerably the volume contraction. Volume measurements performed during absorption and desorption indicate reversible behavior with water, n-propanol, isopropanol, and acetone on virgin wool and irreversibility (hysteresis) with n-butanol on virgin wool and with water on supercontracted wool.
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  • 181
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    Journal of Applied Polymer Science 7 (1963), S. 557-568 
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    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: Equations are derived which relate the pore volume and the volume of pores accessible to sorbate with the constitutive volume vAA, the electrostriction of sorbate by the charged groups of wool vE, and the volume contraction of sorbate in the neighborhood of nonpolar side chains vNP. The pore volume and the volume of pores accessible to sorbate are calculated by use of values of vAA and vE estimated from theory and assuming vNP = 0. The percentage of pores accessible to water increases from 55 to 78 as the pH is decreased from 7 to 2, due to a reversible change which is probably analogous to the reversible unfolding of the serum albumins. Supercontraction in LiBr produces a decrease in the specific volume of wool in n-hexane, the partial specific volume in water, the pore volume, and the volume of pores inaccessible to water. Since analogous changes occur on denaturation of soluble proteins it is proposed that the crystalline regions (containing α-helices) are less dense than the amorphous regions (containing random coils). This is probably due to poorer packing of the diverse side chains in the crystalline regions than in the amorphous regions, since in the latter the chains should be able to bend to accommodate bulky side chains. All evidence available on the accessibility of wool to various sorbates is summarized. Although it is not yet possible to be dogmatic, it is clear that the weight of evidence suggests that wool is approximately equally accessible to water and the lower alcohols.
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  • 182
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    Journal of Applied Polymer Science 7 (1963), S. 569-579 
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    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: A differential thermal analysis device (DTA) for measuring the glass and other polymer transitions is described. A theory on the manner in which a glass transition is manifested in a DTA thermogram, and on the manner for obtaining the real value from the thermogram is presented. Experimental results on polymethyl methacrylate and atactic polypropylene verify the various predictions of the theory.
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    Journal of Applied Polymer Science 7 (1963), S. 581-589 
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    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: Encouraged by the results obtained in the field of graftings between polyvinyl acetate and polyvinyl alcohol, attempts were made to find factors that would bring a polyvinyl acetate emulsion to a higher content of such graftings. In this work vinyl acetate was emulsified and polymerized in water containing polyvinyl alcohol as stabilizer, potassium persulfate as catalyst, and sodium bicarbonate as a buffer. Emulsions were made, with varying degrees of hydrolysis of the polyvinyl alcohol, molecular weight, and pH during the polymerization. Paper chromatography and infrared absorption spectra were used to identify the graftings, but the results proved negative: no graftings were found.
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  • 184
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    Journal of Applied Polymer Science 7 (1963), S. 591-602 
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    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: A mechanism for ultrasonic degradation is proposed as follows. At the contracting step of a violently vibrating bubble in liquid, j structural units of a polymer molecule (partial chain j) take a linearly extended configuration owing to the suction force of bubble, which occurs as a result of slippling and friction between solvent molecules and the extended part of polymer. This partial chain is subject to a tensile force arising from the friction which is maximum at the middle carbon bond of the partial chain. If it is greater than the critical tensile strength of a carbon-carbon bond, the bond at the middle is unable to absorb the work done by it, so the bond is torn off, i.e., the polymer degrades. Under such considerations a formula for the final value of the degree of polymerization after infinite irradiation is deduced, from which the following results are obtained. (1) Cavitation which can degradate polymer molecules effectively is not stationary but nascent. (2) The cavitation intensity is very insensitive to ultrasonic intensity. Moreover, from the proposed mechanism, several experimental facts can be explained: practically monodisperse solution is obtained after long-term irradiation; and ultrasonic degradation occurs even in solutions of infinite dilution.
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  • 185
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    Journal of Applied Polymer Science 7 (1963), S. 617-624 
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    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: A series of poly(acrylhydrazones) has been prepared by the condensation of dihydrazides with dialdehydes and diketones. The dihydrazides included those derived from isophthalic, sebacic, and adipic acids. Terephthalaldehyde, glutaraldehyde, p-diacetylbenzene, and 2,5-hexanedione were the dicarbonyl compounds used. Polymers derived from terephthalaldehyde were of high molecular weight. The polymers varied in crystalinity, fusion point, and solubility in the expected manner. Thermal and hydrolytic stabilities were moderately good. Tough films were cast from a number of the soluble polymers. These films could be isolubilized by reaction with cupric acetate.
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  • 186
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    Journal of Applied Polymer Science 7 (1963), S. 603-615 
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    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: Evidence is presented which suggests that the true gel phase in natural rubber is composed of small crosslinked latex particles (microgel), whose presence is revealed by light scattering and by electron microscopy. These are combined into a matrix with soluble rubber molecules, forming the apparent gel phase. The rate of solution (and hence the apparent gel content) of this phase varies with solvent and is governed by the governed by the diffusion rate of solvent into rubber. Prolonged extraction removes the soluble component. Since the redissolution of the soluble component is very rapid, it is inferred that it is initially bound to the microgel particles by specific forces which have to be overcome by the diffusing solvent. Mastication of crepe breaks up the matrix, leaving microgel particles whose presence can be detected in solution.
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  • 187
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    Journal of Applied Polymer Science 7 (1963), S. 625-641 
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    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: Cellophane sheets were coated with acrylic latex polymers, pressed together in pairs at elevated temperature, and peeled apart at constant relative humidity and temperature. The effect of the rate of peeling and the adhesive layer thickness upon the peeling force was investigated. When a laminate is peeled, the steady-state peeling force is generally not constant, but the frequency distribution of the instantaneously measured steady state force values is Gaussian. The mean value of the force is well defined and is equal to the median force. This type of variability is probably due to sample nonuniformity. The second type of variability in the steady-state peeling force is inherent in the binder/substrate system. Here failure in the glue line is not initiated continuously but periodically, and the failure propagates faster than the rate of peeling. Consequently the steady-state peeling force passes through well-defined maxima and minima. It was also observed that the distance between two adjacent maxima or minima was constant and insensitive to the testing rate. When the force is randomly oscillating, the mean force generally either increases with the rate of testing or is insensitive to it. It always increases with the thickness of the adhesive layer. A special case was extensively investigated where at low rates there was cohesive failure and the peeling force increased with the testing rate, while at high rates the force was rate independent and produced adhesive failure. The cohesive failure force could be represented by a single master curve when the force was plotted against Rtan, where R is the peeling rate, ta is the thickness of the adhesive layer, and the exponent n is a constant characteristic of the system. When the binder/substrate system gives a steady-state force with well-defined periodicity, the maxima and minima in the force generally decrease with increasing testing rate. The periodicity of the steady-state force can be eliminated by having a rough instead of smooth binder/substrate interface.
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    Journal of Applied Polymer Science 7 (1963), S. 667-673 
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    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 dynamic mechanical properties of cured Neoprene Type W gum stock have been measured on a commercial Fitzgerald Transducer from 30 to 3000 cycles/sec. at twelve temperatures from -7.1 to 71.1°C. The results are reduced to 25°C. by the method of temperature-frequency superposition to obtain master curves for real and imaginary components of complex compliance which encompass over ten logarithmic time scales. The shift factors, log aT, are found to obey the WLF equation of log aT = 10.6 (T - T0)/(93.6 + T - T0); T0 = 25.0°C. The equilibrium shear modulus is calculated to be 106.82 dynes/cm.2. The relaxation and retardation spectra are presented. The magnitude of its monomeric frictional coefficient (1.8 × 10-6 dynes-sec./cm.) at 25°C. as well as the implied appearance of the loss tangent peak at relatively high frequency reflect a very high degree of local flexibility. This result appears to be unusual when compared with other common elastomers, e.g., polyisobutylene, vulcanized natural rubber, and Hypalon-20.
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    Journal of Applied Polymer Science 7 (1963), S. 675-683 
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    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 consumption of primary mercaptans from C5 to C12, and of tertiary dodecyl mercaptan, has been studied during chloroprene polymerization. All of the primary mercaptans disappeared with the same rate constant as did the chloroprene monomer. Tertiary dodecyl mercaptan disappeared more slowly. Equal molar concentrations of different primary mercaptans gave similar intrinsic viscosity polychloroprenes at any specific monomer conversion. Polymerization rate and temperature were shown to have little effect on relative mercaptan consumption over the limited conditions employed. The mercaptans studied were shown to have only slight solubilities in aqueous base solutions. The observations led to the conclusion that the mercaptan consumption is not diffusion- or solubility-controlled, but depends upon the inherent reactivity of a mercaptan at the polymerization site.
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    Journal of Applied Polymer Science 7 (1963), S. 1031-1040 
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    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 additions to polyethylene wax on the breaking stress f of butt joints between two steel cylinders depended on the nature of the addition. Oleic acid lowered f in concentrations as small as 0.2%, and in presence of 1% oleic acid f was immeasurably small. Ethyl palmitate slightly diminished f (to about 1/5th of the initial value when the amounts of polyethylene and palmitate were equal), but this decrease was wholly due to the weakening of the polymer itself, and the ratio of f to the tensile strength of polyethylene-palmitate mixtures was 〉1 at all compositions. Thus, with oleic acid above 0.2% improper, and with ethyl palmitate at all percentages, proper adhints were obtained. Stearone apparently formed a weak boundary layer and 4-methyl-2,6-di-tert-butylphenol gave erratic results as it decomposed on heating and apparently reacted with steel. Addition of ethyl palmitate to polyethylene contaminated with oleic acid made the mixture adhesionable. The solubility of the contaminant in solid polyethylene was more important than polarity. The relation between the composition of an adhesive and the breaking stress of its adhints can be understood if the distinction between proper and improper joints is kept in mind.
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    Journal of Applied Polymer Science 7 (1963), S. 1063-1081 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The curing reaction of an epoxy resin and acid anhydride with an amine and/or alcohol was studied kinetically. No etherification reaction occurred at 70-140°C. and the initial reaction rate was proportional to the concentration of epoxide, acid anhydride, and catalyst (tertiary amine or alcohol). The apparent activation energies of the reaction in two systems of epoxy resin-hexahydrophthalic anhydride/triethanolamine (0.5 wt. %) were obtained as 14.1 and 14.4 kcal./mole. The effects of the substitution R of the tertiary amine NR3 or alcohol R3COH as catalyst on the curing reaction of the epoxy resin and acid anhydride were studied. The polar reaction constant ρp for amines, obtained negatively, indicates that electron-repelling substituents of NR3 increase the curing rate; ρp for alcohols, obtained positively, indicates that electron-withdrawing substituents of R3COH increase the rate of curing reaction. These results supported the proposed curing mechanism better.
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    Journal of Applied Polymer Science 7 (1963), S. 2217-2237 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The pyrolysis of a polyurethane obtained from tolylene 2,4-diisocyanate and ethylene glycol was studied in nitrogen, air, and oxygen from the double aspect of structural change and color formation. The dissociation of the polymer into its components followed by further reactions liberates diisocyanate, the corresponding diamine, and the polypseudourea ether, as well as other degradation products. The color is attributed to the yellowing of TDI, the oxidation of the diamine, and the presence of the polypseudourea ether.
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    Journal of Applied Polymer Science 7 (1963), S. 2259-2268 
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    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The crosslinking efficiencies of dicumyl peroxide in SBR, cis-polybutadiene, acrylonitrile-butadiene rubber, and polychloroprene have been measured. For the first two rubbers approximately ten crosslinks are formed per molecule of peroxide decomposed, while for the acrylonitrile-butadiene rubber an efficiency close to unity is found. With polychloroprene approximately two molecules of peroxide are used for each crosslink formed. Analysis of the low molecular weight products of the reaction shows that ease of hydrogen abstraction by cumyloxy radicals decreases in the order given above.
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    Journal of Applied Polymer Science 7 (1963), S. 2249-2258 
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    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: Latices containing 55 parts of styrene, (45 - X) parts of 2-ethylhexyl acrylate, and X parts of methacrylic acid, where X 〉 15, have been shown to yield discontinuous crazed films upon drying. These clear transparent polymer granules upon immersion in water containing a base are peptized to form a reconstituted latex containing spherical particles of the same size as the original latex particles. Inclusion of small amounts of a filming aid in the original or reconstituted latex permits the deposition of continuous polymer films which are rendered water-resistant by baking. The property of redispersibility in water of transparent flakes of polymer is attributed to limited particle coalescence in the polymer grit. The incorporation of relatively high levels of carboxyl groups in the polymer is essential to the redispersion of the polymer by dilute solutions of base. Ionization of the carboxyl groups on the particle surfaces upon addition of a base gives rise to the sudden development of repulsive Coulombic forces which cause particle separation, after which surface forces are sufficient to restore the semiplastic particles to their original spherical shape. Inability to redisperse the film a second time may be due to polymer plasticization or to the migration of carboxyl groups to the particle interior as a result of coalescence forces.
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    Journal of Applied Polymer Science 7 (1963), S. 1153-1163 
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    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: Polyethylene film was irradiated in various atmospheres, i.e., He, Ne, Ar, Kr, Xe, N2, NO, NO2, HO2, CO, CO2, CH4, C2H6, C3H8, and C4H10 by γ-rays from a Co60 source. Xe, Kr, CO, and H2O (vapor) accelerate the radiation-induced crosslinking as recently shown in case of N2O. In addition, saturated hydrocarbon gases seem to be accelerative. NO depresses the crosslinking markedly and CO2, mildly. On the other hand, NO2 decomposes the polyethylene molecule without irradiation. Every other gas appears to be inactive. In relation to the effect of gas atmospheres, we examined their solubilities in polyethylene. N2O is one of the most soluble of the inorganic gases. An electric field was applied to polyethylene film during irradiation. The degree of crosslinking evidently decreases with applied field, whether the atmosphere is N2O or Ar.
    Additional Material: 5 Ill.
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  • 196
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. S30 
    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
    Type of Medium: Electronic Resource
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  • 197
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. S37 
    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
    Type of Medium: Electronic Resource
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  • 198
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1797-1801 
    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: Copolymers were prepared by ester interchange of polyvinylalcohol with ethyl acetoacetate, ethyl benzoylacetate, and ethyl 4-nitrobenzoylacetate. Reaction of ethyl 2,4,6-trimethylbenzoylacetate with polyvinylalcohol yielded a homopolymer. The polymers functioned as chelate ion exchangers. Ion exchange capacities were determined for the polymer derived from polyvinylalcohol and ethyl acetoacetate.
    Additional Material: 1 Tab.
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  • 199
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1803-1814 
    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: Experimental latices of synthetic cis-1,4-polyisoprene and films and cellular objects produced from them are described. The latices of the synthetic polymers with molecular weights of about 2,000,000 are stabilized by anionic surfactants and have weight median particle diameters of about 0.9 μ and log normal particle size distribution. Tensile properties and flow characteristics of unvulcanized latex films could be regulated by introduction of controlled, small, amounts of crosslinking into the latex. Procedures used for crosslink density determination on cis-polyisoprene latex at various stages of use are described. Vulcanized latex films having maximum tensile strengths (5500-6000 p.s.i. and 800-950% elongation) were obtained when the final crosslink density was in the range 1.0-1.6 × 10-4 moles of effective chains/cc. Use of the synthetic cis-polyisoprene latex in production of foam is described. Gelation with sodium silicofluoride at room temperature occurs within 2-10 minutes. Production of a controlled level of crosslinking in the latex prior to frothing and gelling was found to improve the uniformity of cell structure of foams and to increase their resistance to compression. Excessive crosslinking in the latex during maturation was shown to cause a loss of tensile strength in cured products presumably because the coalescence of latex particles during gelation is adversely affected. The properties of synthetic cis-1,4-polyisoprene latices and the physical properties of films and foams derived from them are shown in general to be very similar to those of natural rubber latex and its products.
    Additional Material: 5 Ill.
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  • 200
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1867-1889 
    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 importance and characteristics of viscoelastic fluid behavior are briefly reviewed, as are theoretical predictions of the relationships between the stresses developed in such a fluid and its deformation rate and history. It is seen that most of the equations available for the prediction of these stresses(variously termed “constitutive equations” or “rheological equations of state”) either do not predict the properties of real materials correctly or, alternately, are of such overriding complexity that they cannot be applied to the solution of any but the simplest real problems. A new constitutive equation in which all the significant parameters may be evaluated from only two sets of experiments is developed. Comparison with available experimental results, while not entirely conclusive, indicates that the equation may predict correctly the behavior of nonpolar solutions and polymeric melts and that it may work well on polar systems in the range of high deformation rates, i.e., the region of primary industrial interest. Several problems of interest to the plastics industry are worked to illustrate the use of this constitutive equation.
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