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  • Articles  (1,191)
  • Polymer and Materials Science  (675)
  • General Chemistry  (516)
  • United States
  • 1995-1999
  • 1985-1989
  • 1960-1964  (1,191)
  • 1961  (1,191)
  • Chemistry and Pharmacology  (1,191)
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  • Articles  (1,191)
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  • 1995-1999
  • 1985-1989
  • 1960-1964  (1,191)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 116-123 
    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 molecular weights and molecular weight distribution of a styrene-butadiene rubber produced at 5°C. according to an incrementally modified recipe with tert-dodecyl mercaptan modifier, do not differ significantly from those of similar conventionally modified rubbers. The limiting effect of diffusion upon the mass transfer of mercaptan in the system provides a consistent explanation of this finding.
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  • 2
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), 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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  • 3
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. S4 
    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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  • 4
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 135-148 
    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 work a wide variety of nonionic emulsifiers and anionic/nonionic blends of emulsifiers were evaluated in the emulsion polymerization of vinyl acetate and styrene. It was found that the emulsion stability and other polymer emulsion properties are often dependent upon a certain property of the emulsifier known as the HLB value. It has been shown elsewhere that the HLB value can be correlated with a fundamental physical property of the system oil-water-emulsifier, namely, the spreading coefficient of the internal phase liquid on the surface of a 1% solution of the emulsifier in the external phase. In the emulsion polymerization of styrene, good emulsion stability coupled with adequate conversion rate was obtained in an emulsifier HLB range of 13 to 16. For certain emulsifier blends it was found that emulsion viscosity and emulsion particle size were strongly dependent on the HLB of the emulsifier. Similar comments apply to vinyl acetate polymerization, except that the most stable emulsions were obtained with emulsifiers in an HLB range from 14.5 to 17.5. These observations on preferred HLB range apply only to nonionic emulsifiers and anionic/nonionic emulsifier blends, which were the emulsifier types screened in the present investigation. For both styrene and vinyl acetate the most generally satisfactory emulsion properties were obtained in the present work by the use of an anionic/nonionic emulsifier blend (G-3300/G-3920).
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  • 5
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 149-152 
    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 dependence of grafting on the type of initiator has been examined in the case of three polymer-monomer systems: polystyrene-methyl methacrylate, polymethyl methacrylate-vinyl acetate, and polyethyl α-chloroacrylate-vinyl acetate. The different initiators used in these experiments were benzoyl peroxide (Bz2O2), azobisisobutyronitrile (AIBN), di-tert-butyl peroxide (DTBP), and tert-butyl hydroperoxide (TBHP). In each case the graft copolymers were separated from the homopolymers by fractional precipitation or by extraction. In the case of the system polystyrene-methyl methacrylate, an appreciable degree of grafting as well as formation of graft copolymer occur in the presence of Bz2O2; in contrast, the grafting is low with DTBP and doubtful with AIBN. For the other two systems no noticeable differences occurred as function of the initiator. In the case of polyethyl α-chloroacrylate the amount of graft copolymer is exceptionally high owing to the sensitivity of this polymer to a radical attack; this sensitivity results in the partial insolubility of the graft copolymers in the presence of TBHP and DTBP, but not in the presence of AIBN.
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  • 6
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 157-162 
    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 new synthetic elastomer has been obtained based on an ethylene-propylene copolymer prepared using an organometallic catalyst system. Reactive sites (phosphonyl dichloride groups) are placed on the copolymer chain by treating the polymer with phosphorus trichloride and oxygen. After hydrolysis or alcoholysis of the phosphonyl dichloride groups to phosphonic acid or phosphonic acid esters, vulcanization may be carried out by reaction with metallic oxides, particularly lead oxide. Vulcanizates of the polyolefin elastomer have outstanding resistance to heat, ozone, and oxygen, and have excellent electrical properties. This combination suggests the use of this material in high temperature electrical applications.
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  • 7
    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 cellulose of cotton yarns was reacted with acrylonitrile under conditions preventing their longitudinal contraction. Changes taking place in the fine structure of the fiber were studied by means of optical microscopy, density measurements, x-ray diffraction, and thermal stress behavior measurements. The results indicate that in spite of the strong tensions developed in the yarns, the reaction proceeds in both the accessible and the crystalline regions with considerable volume expansion and eventual disappearance of crystalline structure. Suggestions of a glass transition temperature appear at substitutions slightly above D.S. = 1. Annealing becomes possible at substitutions above D.S. = 2 with the development of the cyanoethyl cellulose crystal structure and over 40% increase in tensile strength. Changes in tenacity, ultimate elongation, energy of rupture, and immediate elastic recovery were also observed.
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  • 8
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 184-190 
    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: Poly(4-methyl-1-pentene) has been prepared by polymerizing the monomer over a catalyst made from titanium tetrachloride and lithium aluminum tetradecyl. The molecular weight of the crystalline polymer was invariably too high for fiber preparation, even when polymerization variables were varied drastically, so a technique for thermal cracking was developed. By heating grease-free, crystalline poly(4-methyl-1-pentene) in a vacuum at about 280°, it was possible to lower smoothly the molecular weight of the polymer to any desired value, without undesirable crosslinking or by-product formation. The polymer was melt-spun by conventional techniques to highly oriented, tough fibers. Copolymerization of 10-25% 1-hexene and other linear 1-olefins with 4-methyl-1-pentene gives products which are still high-melting, but which are readily soluble in such solvents as cyclohexane or chloroform, in contrast to the homopolymer which is only slightly soluble. Polymerization in solvents for the copolymer gave solutions which were converted to fibers and film without intermediate isolation of polymer or removal of the catalyst. An interesting terpolymer in which divinylbenzene was the third component was found to be initially soluble, but was readily crosslinked at elevated temperature.
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  • 9
    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: Treatment of unaccelerated natural rubber-sulfur vulcanizate networks with triphenylphosphine in benzene at 80°C. effects the removal of part of the combined sulfur, the proportion removed decreasing with increasing cure time. This partial desulfurization of the network is attributed, on the basis of the mode of interaction of simple organic di- and polysulfides with triphenylphosphine, to the conversion of polysulfide linkages in the network into either mono- or disulfide groups. Knowledge of the amount of sulfur removed by the reagent, and of the chemical degree of crosslinking and combined sulfur content of the untreated networks permits the following semiquantitative conclusions to be reached concerning the structures of the sulfur linkages in the networks: (1) long polysulfidic crosslinks (—S11— to —S12—) are initially formed, which on continued cure progressively decrease in length to a limiting value of —S2— to —S4—; and (2) a very high proportion to the combined sulfur (ca. 77% for short cure times, increasing to ca. 95% on extended cure) is present in cyclic monosulfide groups situated along the polyisoprene chains.
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  • 10
    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: An empirical equation relating glass temperature, molar cohesion, and polymer structure has been developed from data found in the literature. A fairly extensive list of group cohesion values has been obtained from this relationship and glass temperatures which are in good agreement with reported values have been calculated. The equation is $$ H_c = 0.5nRT_g - 25n $$ where Hc is the molar cohesion and n is an empirical number obtained from the polymer structure.
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  • 11
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 452-459 
    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 styrene derivatives vinylbenzyl chloride and isopropenylbenzyl chloride were prepared and copolymerized with isobutylene and propylene in order to produce polymers with reactive halogens. Vinylbenzyl chloride and isobutylene have relative reactivities such that the copolymer is much richer in isobutylene than the starting mixture, while with isopropenylbenzyl chloride and isobutylene the difference in reactivities is less and is in the opposite direction. Copolymers containing small amounts of the reactive benzylic chlorine were vulcanized, either with amines or with a conventional butyl rubber cure. Permselective membranes were prepared from copolymers rich in benzylic chlorine.
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  • 12
    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 necessity for oven post-curing Viton A vulcanizates is explained in the following way: The formation of crosslinks is accompanied by the elimination of HF from the polymer. In the subsequent reaction of HF with the magnesium oxide present as acid acceptor water is formed which acts to inhibit the full development of cure unless it is removed from the vicinity of the polymer by post-curing in an open system. Measurement of the rate of elimination of water from the polymer serves as a method of following the development of crosslinking during cure. Approximately two moles of water, derived from four moles of hydrogen fluoride, are associated with the use of one mole of diamine curing agent. This ratio is confirmed by independent estimates of the relationship of crosslinking density to curing agent level based on measurements of swollen compression moduli.
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  • 13
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 349-353 
    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: Calendered sheets of pale crepe rubber containing an ultra-accelerator, piperidinium N-pentamethylenedithiocarbamate, and zinc oxide were embedded in powdered sulfur and kept at room temperature. Tensile strengths up to 294.2 kg./cm.2 (4185 psi) and elongations up to 530% were attained; the combined sulfur in 115 weeks was 3.60%. Calendered pale crepe rubber containing 10 parts of yellow mercuric oxide to 100 parts of rubber allowed to stand covered with quinone dioxime (GMF) powder at room temperature slowly vulcanizes, reaching a tensile strength of 53.1 kg./cm.2 (754 psi) in 405 days, and retaining this condition for at least twice this same period of time. The elongation reached 740%, and the set was 0.16. The tensile strength obtained is almost as high as that obtained in a press cure with quinone dioxime alone. The untreated sample containing yellow mercuric oxide alone showed a tensile strength of only 5.3 kg./cm.2 (75 psi). Calendered pale crepe with no mercuric oxide set in quinone dioxime and calendered pale crepe containing 2 parts of quinone dioxime, when allowed to stand at room temperature, showed no signs of vulcanization.
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  • 14
    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: Viscose-grade cotton linters (DPw = 1135) were converted to viscose by the emulsion xanthation technique. Two variables - namely, substitution level and xanthation time - were considered insofar as their influence on the uniformity of substitution with regard to chain length was concerned. The stable diethylacetamide derivatives were prepared by reaction with diethylchloroacetamide and fractionally precipitated from aqueous 2-chloroethanol. The DPw and degree of substitution (DS) of the individual fractions were determined. The results in each case indicated that the longer chains were more highly substituted than the shorter chains. For a constant xanthation time (6 hr.), uniformity in substitution improved with increasing substitution level. For a constant CS2:cellulose ratio (1.48), uniformity increased with xanthation time. A mechanism is suggested which accounts for these phenomena.
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  • 15
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 354-363 
    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 elution method is essentially a single-stage process, whereas the thermal gradient method is a multistage process which depends upon a thermal gradient to bring about reprecipitation of polymer in the fractions. As a test of the effectiveness of the thermal gradient, comparisons have been made of fractionation by these two column methods on high molecular weight polystyrene samples. It was found that the thermal gradient method definitely provides superior resolution and reproducibility, as expected. However, the degree of fractionation obtained by the elution method was surprising, accounting for at least 80% of the sample under the usual conditions and giving complete fractionation with certain modifications of conditions. These results indicate the difference in performance of the two methods is less than expected from an elementary consideration of the operation of the columns, and fractionation by the elution method, as conducted here, exceeds that expected for a single-stage extraction process. Although the reasons for the observed behavior are not clear, the following conclusions have been reached about certain factors which influence fractionation. Alternative methods of controlling the concentration of polymer in the fractions give almost equivalent results but enhanced resolution of the high molecular weight portion of the sample is obtained with extended solvent gradients. The inhibitor, tert-butyl catechol, which it was necessary to add to the solvents to limit degradation of the very high molecular weight sample, plays a specific role in the fractionation due to a reaction with the polystyrene which alters the fractionation behavior without affecting the molecular weight. Also, trace amounts of chemical heterogeneity in the polymers, presumably hydroxyl groups, have a marked adverse effect on fractionation by the elution method and probably account for molecular weight reversals observed in some fractionations by the thermal gradient method. It is suggested that adsorption on the surface of the beads is responsiblp for the adverse effect of chemical heterogeneity on the fractionation and that possibly an adsorption which increases with molecular weight contributes to fractionation by the elution and thermal gradient methods.
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  • 16
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    Journal of Applied Polymer Science 5 (1961), S. 375-383 
    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 effects on viscose ripening of a variety of materials are reported. (1) Normal constituents (Na2CO3, Na2CS3, NaCl) appeared not to affect ripening; however, Na2S retarded ripening. By-product removal appeared to retard ripening. (2) Oxidizing agents (H2O2, Na2Sx) accelerated ripening; reducing agent (Na2SO3) retarded ripening; this is suggestive of possible addition product formation. (3) Na2SO4, (CH3)2SO, KClO3, Na2BH4 showed no effect on ripening. (4) Salts which precipitated as hydroxides or carbonates did not appear to affect ripening. (5) Salts which formed insoluble sulfides resulted in an initial increase in ripening rates. In later stages, ripening proceeded normally, probably after the salts were removed from solution as insoluble sulfides. (6) FeCl3, BiCl3 and Na3AsO3 appeared to retard ripening. (7) A comparison of the effect on ripening of the trivalent state of elements in group V of the periodic table showed that the rate of ripening decreased with the oxidation potential of the element. (8) The addition of sodium zincate retarded ripening and suggested possible cross-linking of xanthate and by-product sulfur, or of two xanthate groups. (9) Addition of tin and chromium salts at the 0.5% level resulted in gelation of the viscose within 30 min. after the addition.
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  • 17
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 388-396 
    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 crosslinking of internally plasticized polyvinyl chloride-stearate copolymer by irradiation with high-energy electrons was studied. Based on gel yields and swelling as a measure of relative crosslinking, the effect of added tetra-functional monomers, and of carbon black and silica fillers are discussed. Crosslinking by dicumyl peroxide a t 170°C. even in the presence of a stabilizer, causes concurrent decomposition (dehydrochlorination) which is avoided in the radiation-crosslinking process. The heat stability of the copolymer is not impaired by radiation crosslinking under the proper conditions. Results of tensile measurements a t 25 and 150°C. are given for the radiation-crosslinked copolymer with and without filler reinforcement.
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  • 18
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    Journal of Applied Polymer Science 5 (1961), S. 401-407 
    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: As the accelerating effect of water in the crosslinking reaction of rubber in natural latex by γ-irradiation was assumed to stem from the decomposition of water into radicals by γ-irradiation, more effective reagents were sought among the organic halides which have greater G values for radical formation by γ-irradiation and, simultaneously, an affinity for rubber greater than that of water. 1,2-Dichloroethane, chloroform, carbon tetrachloride, and benzene (for comparison) were tested, and these compounds, except for benzene, were found to accelerate the reaction in proportion to their G values for radical formation. Benzene was found to have no effect, in concentrations between 1 and 5 phr. The optimum dosage was decreased to 2.1 × 106, 1.0 × 106, and 7.6 × 105 r by the addition of 1, 3, and 5 phr of carbon tetrachloride, respectively, and was assumed to have decreased to 1.17 × 107, 9.0 × 106, and 7.6 × 106 r with 1, 3, and 5 phr of 1,2-dichloroethane, and to 8.6 × 106, 6.2 × 106, and 5.2 × 106 r with 1, 3, and 5 phr of chloroform, respectively. The physical properties of the films obtained at the optimum dosages under these accelerating conditions were equal to those of the latex irradiated up to the optimum dosage with no addition of halide. No side reactions occurred during the halide-accelerated crosslinking that were sufficiently extensive to influence the infrared spectra.
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  • 19
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    Journal of Applied Polymer Science 5 (1961), S. 424-427 
    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 polyaddition process involving a hydroxy-terminated linear polyester and an organic diisocyanate in the presence of a series of metal acetylacetonates has been investigated. The method involved kinetic analysis of plasticity build-up in a Brabender Plastograph. Catalytic orders and relative catalytic constants (kc/k0) were determined for Mn(Aa)3, VO(Aa)2, V(Aa)3, Fe(Aa)3, Cu(Aa)2, Co(Aa)3, and Cr(Aa)3; the constants decrease in that order. Catalytic orders are unity for all complexes save manganese, which is 1.75. No correlation between dissociation potential and catalytic coefficient has been found, and it is believed that catalysis may be associated with the paramagnetic properties of the metal.
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  • 20
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    Journal of Applied Polymer Science 5 (1961), S. 428-435 
    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: Dynamic Young's moduli are derived from observations of wave propagation in stretched filaments of natural and butyl rubbers. Extensions up to about 700% are studied within a temperature range of -45 to +50°C. and a frequency range of 0.2 to 20 kycles/sec. At constant temperature and frequency both the real (E') and imaginary (E″) components increase with increasing extension. The loss factor (E″/E') decreases with increasing extension, but the decrease is more pronounced for the butyl rubber so that the large difference in damping between the two polymers in the unstrained state is greatly reduced at high extensions. Approximate relaxation spectra are derived for the strained materials on the basis of several assumptions regarding the applicability of the WLF equation. It is found that the spectra are displaced in the direction of longer times by increasing extension; this is equivalent to an increase in the monomeric friction coefficient with extension. The effect is more pronounced for the natural rubber than for the butyl, and consequently the ratio of the friction coefficients (butyl:natural) falls from several hundred unstrained state to approximately 3 at 550% extension.
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  • 21
    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: Investigations of the viscoelastic aspects of the mechanical behavior of polymers have been limited almost exclusively to relatively simple conditions of homogeneous stress, that is, to tension or shear loadings. In the present work a study has been made from the viscoelastic standpoint of the response of several elastomers to a much more complex type of stress distribution arising from penetration up to failure by a cylindrical indentor for a range of temperatures and rates of penetration. The failure or “puncture point” was determined by a dip in the recorded curve of load versus depth of penetration. The puncture strength values were reduced to 25°C. by applying the ratio of absolute temperatures and plotted against the logarithm of the reciprocal of the rate of penetration. These curves were then shifted on the time scale to give a master curve after the manner of Tobolsky and of Ferry. The logarithms of the shift factors thus obtained were related to the reciprocal of the absolute temperature over the range studied. The results indicate a broader generality for the viscoelastic principle of time-temperature equivalence than has usually been supposed.
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  • 22
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    Journal of Applied Polymer Science 5 (1961), S. 612-619 
    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 an attempt to extend the outdoor serviceability of items molded from linear polyethylene and copolymers, three ultraviolet absorbers, namely, Cyasorb UV-9 (2-hydroxy-4-methoxybenzophenone), Cyasorb UV-314 (2,2′-dihydroxy-4-n-octoxybenzophenone), and TBS (4-tert-butyl phenyl salicylate), sixteen different pigments, and combinations of both ultraviolet absorber and pigment were investigated. Injection-molded test specimens were employed in this study. The laboratory source of radiation to which these samples were exposed was an Atlas XW Weatherometer. Similar samples also were exposed at various outdoor locations including Phoenix, Arizona, Summit, New Jersey, and Newark, New Jersey, to utilize practical conditions of outdoor weathering. During these weathering studies surface cracking was observed as occurring at approximately the same time as a significant decrease in tensile strength, elongation, and melt index. Such observations became a method of rapidly screening a large number of formulations for resistance to ultraviolet radiation. For optimal outdoor serviceability with respect to retention of elongation, tensile strength, and melt index properties of molded items, the following steps are necessary. A high-density resin having as low a melt index as possible is selected. The molded item is designed to minimize the formation of molded-in stresses and strains. Proper selection of UV absorbers, pigments, and combinations of both are made. Pigments such as green, orange, peacock blue, monastral purple, red, and black, in high concentrations, will prolong the outdoor weatherability of a given product.
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  • 23
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    Journal of Applied Polymer Science 5 (1961), S. 647-654 
    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 viscoelastic properties of regenerated cellulose containing several different softeners or water only were investigated. Measurements of creep and Young's modulus were made on the Instron tensile tester, and the creep curves were fitted to a mechanical model consisting of Voigt and Maxwell elements of springs and dashpots in series. The elastic and viscous parameters were determined for the various softened films and compared with each other and with measurements of Young's modulus. It was found that the elastic modulus is a function of the effective molar concentration of the softener in the film which is related to its ability to break hydrogen bonds. The inelastic deformation was found to be a linear function of the heat of vaporization of softener (including water) in the film which is related to hydrogen-bonding energy. Thus, inelastic deformation requires breaking of interchain hydrogen bonds in contrast to pure elastic deformation which involves stretching of hydrogen bonds. A relationship of the Voigt unit and of the Maxwell unit on the composition of the cellulose-softener system and on cellulose-softener interaction has been demonstrated.
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    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 exocellular polysaccharide fermented from glucose in good yield by Xanthomonas campestrìs NRRL B-1459, has been characterized. The general aspects of chemical constitution have been established, as well as the physical properties related to practical applicability. This macromolecular polysaccharide is composed of D-mannose, D-glucose, D-glucuronic acid (as the potassium salt), and a small proportion of acetyl groups. It can be produced on an industrial scale and is stable is storage. Analytical fractionation indicates fairly sharp molecular distribution for the native polysaccharide. The polysaccharide forms homogeneous dispersions in water which show plastic rheological properties and viscosity comparable with that of high-grade plant gums. Outstanding characteristics of practical significance are the atypical insensitivity of solution viscosity to salt effects and to heat, especially when salt is present. Solutions of low concentration show a restricted viscosity decrease upon salt addition; those of higher concentrations show substantial increases. Viscosity is enhanced still further by monovalent cations at basic pH and by divalent cations at neutral or slightly basic pH. Salt moderates or eliminates any viscosity decrease due to heat and, in somewhat higher concentrations, it increases the viscosity of heated solutions. Heating or deacetylating Polysaccharide B-1459 causes no impairment of its properties, but actual improvement. The constitutional basis for these unusual properties is discussed.
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    Journal of Applied Polymer Science 5 (1961), S. 527-533 
    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 system is described for automatic collection of stress-strain data for polymeric films on magnetic tape for subsequent automatic data reduction and computation of a variety of stress-strain parameters. Two shaft analog-to-digital encoders attached to a conventional tensile tester feed digital information to an incremental pulse recorder which stores all stress and strain data in two channels on 0.625-in. magnetic tape. Specimen information and test constants are inserted by the operator through a keyboard located at the tensile tester. The tape is subsequently fed into a standard digital computer through a special incremental pulse magnetic tape reader. The data pulses are internally stored and converted by means of a special program into eight significant stress-strain parameters for polymeric film samples, plus averages and standard deviations for groups of replicate determinations. These parameters include: corrected length of specimen, initial maximum tensile modulus, offset yield stress, strain at break, strain at maximum stress, maximum tensile stress, tensile stress at break, and work to break. While the program described applies to polymer film testing, both it and the digital recording equipment accessories are applicable with suitable modification, to any analog experimental data. Significant savings in man-hours and increased information output result from use of this system.
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    Journal of Applied Polymer Science 5 (1961), S. 545-552 
    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 effects on mechanical properties of heterogeneous acetylation and methylation of isotropic cellulose films have been studied. The effects on breaking load, extensibility, yield point, elastic recovery, and initial Young's modulus in the air-dry state were very small. It is concluded that these properties are not markedly influenced in cellulose derivatives by variation of the nature of the intermolecular cohesive forces in the way that might have been anticipated from the analogy of a simple molecular network. It is suggested that the lack of effect of such treatments, and also the cause of the low elastic recovery in cellulose and its derivatives, may be connected with molecular stiffness, dipole distribution, and supracrystalline structure. Cellulose and its derivatives are contrasted with nylon in this respect. The effects of methylation or acetylation on mechanical properties in water are much more extensive and are attributed to a solubilizing effect which, in the case of progressive acetylation, is ultimately opposed by the formation of acetate-acetate intermolecular bonds that are relatively stable to water.
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    Journal of Applied Polymer Science 5 (1961), S. 580-588 
    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: Torsional modulus-temperature data have been obtained on heterogeneous polymer compositions prepared by several procedures. Both the state of aggregation of the component chain molecules and their degree of compatibility are significant variables. Modulus curves similar to those for crystalline polymers can be obtained from incompatible polymers having glass temperatures sufficiently far apart. Detailed interpretations are presented for modulus curves of both individual homopolymers and bicomponent heterogeneous polymer mixtures.
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    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
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    Notes: Improvements in physical properties of polyvinyl alcohol fibers were attempted by means of both crosslinking and graft copolymerization. By using the ceric iron redox system on synthetic fibers spun from polymer blends containing polyvinyl alcohol (PVA) and its partially (about 15 mole-%) N-methylolcarbamoylethylated products (PVM) in which the blend ratios were 0/100, 10/90, 15/85, and 20/80 by weight, methyl methacrylate (MMA) was grafted at 30°C. in the aldehyde-free acetone-water system after crosslinking by heat treatment or successive acid treatment. Grafting increases with increasing PVM component. This may be ascribed to the coarsening of the fiber texture caused by polymer blending and the increasing of methylol groups as a reducing agent. Moisture regains decrease with increasing graft fraction, but these appear to be greater than the additive values of backbone and graft polymer. Less shrinkage in boiling water is obtained with the increase of PVM component and grafting; the decreased shrinkage is significant in the acid-treated PVM-PVA fibers, and it reaches a nearly sufficient value at about 50% graft-on. The PVA fibers do not give sufficient shrink-proofing. The inherent tenacity and elongation of the grafted fibers increase slightly with increasing graft-on or denier except at the high grafting above about 100, 150, and 300 in the PVA, acid-treated, and acid-untreated PVM/PVA fibers, respectively; whereas the tensile strength in grams/denier decreases with grafting. Although at high grafting, a destruction in the fiber texture will perhaps occur, the coarser the texture of backbone fiber, the harder the change by grafting. The knot/normal ratios in tensile strength or elongation of the grafted fibers have been retained at above 90%. The elastic recovery of the grafted fibers is considerably improved as compared to the conventional Vinylon fibers. The improvements in the acid-treated and grafted PVM/PVA (20/80) fibers are significantly greater above and below 50% graft-on, especially in the range of lower extension. As expected, the thermosetting property is also appreciably imparted with grafting. In the conventional Vinylon fibers, the formalization for shrink-proofing is usually at a sacrifice of elastic recovery. But MMA grafting in the PVM/PVA fibers gives a fairly good elastic recovery and less shrinkage in addition to thermosetting property, making the most of the characteristics in the longer intermolecular crosslinkages formed between methylol groups or PVA-OH groups and methylol groups.
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    Journal of Applied Polymer Science 5 (1961), S. 620-620 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    ISSN: 0021-8995
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    Journal of Applied Polymer Science 5 (1961), S. 704-713 
    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 has been made of the reactions of cellulose with formaldehyde under acid conditions, where the fabrics are baked at elevated temperature. These treatments have involved cotton cellulose in a “dry” or relatively unswollen state and have resulted in the treated fabrics exhibiting improved crease rccovery both dry and wet. It has been found that boiling 1% acetic acid solution reduces the acetal contents of the treated fabrics and causes corresponding decreases in both dry and wet crease-recovery improvement. The reproducibility of these treatments, with respect both to extents of formaldehyde incorporation and to dry and wet crease recovery, is found to be very good within a single treatment and, more importantly, tietween different treatments carried out under the same conditions. The rates of acetal removal by the boiling 1% acetic acid and the relationships between acetal content and crease-recovery improvement have been found to be fairly complex. A study has also been made of the rates of acetal removal by boiling 1% acetic acid for samples of cotton card sliver treated with acid and subsequently heated in sealed tubes with paraformaldehyde. The rates of acetal removal in this case have been observed to be qualitatively similar to those observed for treated fabrics. The implications of these findings are discussed.
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    Journal of Applied Polymer Science 5 (1961), S. 753-753 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Zeitschrift für die chemische Industrie 73 (1961), S. 26-26 
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    Zeitschrift für die chemische Industrie 73 (1961), S. 1-7 
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    Keywords: Chemistry ; General Chemistry
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    Notes: Es wurden die Schüsse der Bombardierkäfer Brachynus sclopeta Fabr., Br. explodens Duft. und Br. creptians L. Untersucht und als ein Gemisch aus p-Benzo- und Toluchinon erkannt. Die gleichen Stoffe konnten im Hinterleib von zwei getrockneten Exemplaren einer afghanischen Pheropsophus-Art (Ph. catoirei Dej.) nachgewiesen werden. Die Chinone entstehen in einer explosionsartig verlaufenden, enzym-kataly-sierten Reaktion aus den entsprechenden Hydrochinonen und Wasserstoffperoxyd. Der gleichzeitig frei werdende Sauerstoff liefert den zum Ausschleudern und Zerstäuben nötigen Druck.
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    Notes: In einer Übersicht über die neueste Literatur wird die Bildung von Carbenen durch Zersetzungs- und Eliminierungsreaktionen besprochen. Einschiebung, Addition und innermolekulare Umsetzungen sind Haupttypen der Carben-Reaktionen. Abschließend wird auf Fragen des Elektronenzustands und Energieinhalts der Carbene eingegangen.
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    Zeitschrift für die chemische Industrie 73 (1961), S. 220-220 
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    Zeitschrift für die chemische Industrie 73 (1961), S. 186-197 
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    Notes: Neben das Hochdruckpolyäthylenverfahren, das von der ICI gefunden wurde, sind in den letzten Jahren Mitteldruck- und Niederdruck-Äthylenpolymerisationsverfahren getreten (Phillips Petroleum, Ziegler). Beim Hochdruckverfahren erfolgt das Kettenwachstum nach einem radikalischen Mechanismus, beim Phillips- und Ziegler-Verfahren nach einem ionischen. Mit Hilfe von Ziegler-Katalysatoren stellte Natta kristallines Polypropylen her2). Der Umfang der Polypropylen-Produktion nimmt stark zu. Neben den Homopolymerisaten (Polyäthylen + Polypropylen) haben Olefinmischpolymerisate bis jetzt geringere wirtschaftliche Bedeutung, doch ist mit steigendem Interesse an den Mischpolymerisaten zu rechnen, besonders an den Paaren Äthylen-Propylen und Äthylen-Butylen. Aus diesen Paaren läßt sich bei Anwendung verschiedener Ziegler-Katalysatoren durch Variation des Monomerenverhältnisses und der Polymerisationsbedingungen ein breites Spektrum von Eigenschaften der Mischpolymerisate herstellen. Man kann hochkristalline (harte), mittelkristalline (flexible) und amorphe (kautschukartige) Substanzen herstellen. Durch peroxydische Vernetzung der amorphen Mischpolymerisate erhält man Vulkanisate mit guten gummitechnischen Eigenschaften und ausgezeichneter Oxydationsbeständigkeit. Sulfochlorierte Mischpolymerisate zeigen interessante anwendungstechnische Eigenschaften. Mit Hilfe spezieller Ziegler-Katalysatoren und bei Anwendung der Methode der Periodenmischpolymerisation ist es möglich, „Blockpolymerisate“ aus verschiedenen Olefinen herzustellen.
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    Notes: Diese Arbeitstechnik ist zur gaschromatographischen Untersuchung hochsiedender Flüssigkeiten oder Festsubstanzen (Hochpolymeren) geeignet, kann aber auch bei der Reaktionsgaschromatographie angewandt werden. Man schmilzt die Probe in eine evakuierte Glasampulle ein und unterwirft sie dann z. B. einer schonenden Pyrolyse oder Hydrolyse. Anschließend wird die Ampulle zertrümmert und deren Inhalt mit dem Trägergas in den Gaschromatographen gespült. An der Zersetzung von Polyoxymethylenen wird die Arbeitstechnik erläutert; die hier erzielte Genauigkeit liegt bei etwa 1%.
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    Zeitschrift für die chemische Industrie 73 (1961), S. 687-687 
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    Zeitschrift für die chemische Industrie 73 (1961), S. 806-806 
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    Notes: Die bei Verbindungen der Systeme Oxyd-Wasser erzielten neuen Ergebnisse ermöglichen eine Systematik, die das gesamte Gebiet unter Berücksichtigung der drei Aggregatzustände unter einem einheitlichen Gesichtspunkt zusammenfaßt. Nach der Art der Wasserbindung werden vier Haupttypen unterschieden: Hydroxyde, Oxydhydrate, Hydronium-Verbindungen und Oxydaquate. Der Stand der Forschung wird in den Kapiteln „Gasförmige Hydroxyde“, „Verbindungen durch hydrothermale Synthese“, „Niederwertige Hydroxyde der Übergangsmetalle“ und „Aufbau von festen Aquoxyden“ beschrieben, die als Schwerpunkte der modernen Entwicklung des Gebietes angesehen werden.
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    Zeitschrift für die chemische Industrie 73 (1961), S. 589-597 
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    Notes: Zahlreiche Verbindungen des Schwefels, vor allem solche mit Stickstoff und Sauerstoff, sind ringförmig gebaut. Bevorzugt treten sechs- und achtgliedrige Ringe auf; fünfgliedrige Ringsysteme sind bei Metallthionitrosylaten bekannt. Es wird ein Überblick über Darstellung, Eigenschaften und Bindungsverhältnisse gegeben.
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    Zeitschrift für die chemische Industrie 73 (1961), S. 612-615 
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    Notes: Es wird eine Methode des fraktionierten Kristallisierens und Schmelzens beschrieben, die wie die Kolonnendestillation ein echtes Gegenstromverfahren darstellt. Das neue Trennverfahren kann zur Reinigung von unzersetzt schmelzbaren, kristallisierenden Verbindungen und zur Trennung von Mischkristallsystemen dienen. Verglichen mit dem Zonenschmelzen führt es sehr viel schneller zu reinen Substanzen, wie Versuche mit Stearylalkohol, Cetylalkohol und 2.4-Dinitrotoluol ergaben.
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    Zeitschrift für die chemische Industrie 73 (1961), S. 603-611 
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Drehungsvermögen und Zirkulardichroismus sind eine Folge der Wechselbeziehungen zwischen dem elektromagnetischen Feld polarisierten Lichtes und optisch aktiven Verbindungen. Der Zirkulardichroismus steht in enger Beziehung zur energetischen Seite der Erscheinung, denn er gibt den Unterschied der Absorption von rechts- und links-zirkular polarisiertem Licht durch die asymmetrischen Moleküle wieder. Es wird eine Registrier- und Meßapparatur beschrieben, die die Aufnahme des Dichroismus zwischen 220 und 600 mμ erlaubt. Ferner werden die Ergebnisse der Untersuchung von gesättigten und ungesättigten Steroidketonen mitgeteilt. Die Methode eignet sich weiter für quantitative Bestimmungen optisch aktiver Substanzen.
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    Zeitschrift für die chemische Industrie 73 (1961), S. 597-602 
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    Notes: Viele natürlich vorkommende und synthetische Verbindungen zeigen antihämorrhagische Wirkung. Es sind vor allem Naphthalin-Derivate mit unsubstituierter 3-Stellung oder solche, die eben dort eine  -  meist aliphatische  -  Seitenkette tragen. Entscheidendes Intermediärprodukt des betr. Stoffwechsels ist sehr wahrscheinlich das Methyl-naphthochinon, die entscheidende Wirkform das Vitamin K2(20). Die K-Vitamine dürften neben ihrer auffälligen Wirkung an einem mehr oder weniger allen Zellen gemeinsamen Stoffwechselprozeß beteiligt sein, sehr wahrscheinlich an der Atmungskettenphosphorylierung.
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    Zeitschrift für die chemische Industrie 73 (1961), S. 615-619 
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    Topics: Chemistry and Pharmacology
    Notes: Die Radiogaschromatographie 14C- und 3H-markierter Substanzen eignet sich zur Identifizierung und Kontrolle bestrahlungsmarkierter Verbindungen, zur Untersuchung radiochemischer Präparate, organischer Reaktionen und ihrer Mechanismen und biochemischer Reaktionsketten sowie zum Studium von Isotopeneffekten. Zur Messung dient die Kombination von Gaschromatograph mit Durchflußionisationskammer und Vibrationselektrometer bzw. mit einem Durchfluß-Proportionalzählrohr oder dem Flüssigkeits-Szintillations-Spektrometer. Es wird eine Durchflußionisationskammer beschrieben, die 10-2 μc 14C und 3H als Grenzaktivitäten zu bestimmen vermag.
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    Zeitschrift für die chemische Industrie 73 (1961), S. 619-620 
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