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  • Polymer and Materials Science  (70)
  • 1960-1964  (70)
  • 1961  (70)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    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.
    Additional Material: 8 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 55 (1961), S. 145-152 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the reaction of aluminum alkyls or aryls with (C5H5)2TiCl2 or (C5H5)2Ti(C6H5)2, there is rapid exchange of groups between the aluminum and titanium centers. When mixed alkyl and phenyl aluminum compounds react competitively with (C5H5)2TiCl2 to form ethylene polymerization catalysts, alkyl groups are more efficient than phenyl groups in initiating polymer chains. Since there is both selectivity in the initiation step and rapid exchange of groups, the presence or absence of phenyl endgroups in the polymer formed from different phenyl-containing catalysts cannot be used to identify the active catalyst site, as has been proposed. Additional evidence is presented which suggests that the π-bonding of the cyclopentadienyl compounds is disrupted either wholly or in part under the polymerization conditions, and at least part of the catalytic activity is due to the decomposition products.
    Additional Material: 1 Ill.
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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymerization characteristics for 1-acrylamido-1-deoxy-D-glucitol and of 1-deoxy-1-methacrylamido-D-glucitol with various vinyl monomers is given. For the former compounds Q and e values are found to be 0.12 and 0.6 respectively and, for the latter, 0.08 and 1.3. In addition, viscosity, osmotic molecular weights, and solubilities for representative compounds are given.
    Additional Material: 1 Ill.
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  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reported preparation of methyltitanium trichloride has been refined to give a product free of aluminum compounds. The infrared spectrum of this material in the 2-15 μ region was recorded, and suggested assignments for the various vibrations are given. Aluminum-free methyltitanium trichloride is not a catalyst for the low-pressure polymerization of ethylene, but it forms an active catalyst in the presence of its lower valence, thermal decomposition products. Mixtures of methyltitanium trichloride with vanadium tetrachloride or vanadium oxytrichloride lead to reduction of the vanadium valence and are active polymerization catalysts. In these bimetallic cases, polymer growth seems to occur at the vanadium center.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 52 (1961), S. 331-339 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The interfacial polycondensation method is one of the main achievements recently made in the chemistry of high molecular compounds. Its theoretical importance and the expected practical results aroused considerable interest in the method. By its means polyamides, polyesters and polyurethanes have been synthesized. The present report is devoted to a presentation of the results of an investigation into the interfacial synthesis of polyureas. The synthesis was carried out starting from the diamines and phosgene: In this particular case the diamine used was hexamethylenediamine. The reagents were brought in contract in the form of their solutions, namely in aqueous alkali in the case of the amine and in various organic solvents in the case of phosgene. The effect of the solubility of the phosgene solvent in the hexamethylenediamine solvent (water) on the yield and reduced viscosity of the polyureides was investigated. It was found that with increase in solubility both the yield and the viscosity decreased. The influence of the molar ratio of the reagents, of excess NaOH, of the solution concentration, of the duration of reaction, of the temperature, on the degree of polymerization and reduced viscosity of the polymers was also studied. A decrease of the temperature flavors growth of molecular weight. For temperatures between 10°C. and -10°C. the viscosity varies within the limits 0.08 to 0.7.
    Additional Material: 10 Ill.
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  • 6
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 337-348 
    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 predicted general incompatibility of mixtures of polymers has been further confirmed. Thirty-one mixtures of homopolymer pairs showed phase separation in a common solvent. These included closely related polymers such as polyacrylates with both polymethacrylates and other polyacrylates and pairs of different polymethacrylates. Typical immiscible combinations are PMA/PEA and PEMA and PEMA/PMMA. It was also found that the presence of a common monomer constituent did not result in complete compatibility of either a homopolymer with a copolymer or a mixture of two copolymers. Apparently, none of the combinations tried were sufficiently similar to result in heats of interaction small enough to be counteracted by the small entropy change involved. Since another possibility for attaining miscibility is through polar interactions, the effects of ionic and hydrogen-bonding substituents upon polymer-polymer compatibility were considered, and selected experiments were done on a series of carboxyl-containing polymers and their sodium salts. It was concluded that hydrogen bridging occurs preferentially either intramolecularly or between polymer and solvent rather than between two different types of chains each having hydrogen-bonding ability. Thus, poly(acrylic acid) and poly(methacrylic acid) show two-phase separation in water. Although poly(sodium acrylate) and poly(sodium methacrylate) are completely miscible, mixtures of the partially neutralized acids, e.g., PAA and PNaMA mixtures, show separation. In contrast to predictions for less polar polymers, compatibility of mixtures of polymers containing high mole fractions of carboxylic acid monomers showed a pronounced dependence upon solvent. Thus, the two copolymers 45/53 EA-MAA and 47/53 MMA-MAA are incompatible in methanol or ethanol but form homogeneous solutions in DMF or DMS.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    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.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. S15 
    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: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 663-667 
    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: Rayon monofilaments containing 80% activated carbon were prepared. They are an effective medium for adsorbing noxious odors. High grade gas-adsorbing carbons are intimately bound in a cellulose matrix by niising the carbon in viscose ‘sodium cellulose xanthate solution’ and extruding the mixture through a special conjugate jet as iiioiiofilaments into a rayon coagulating bath. The special jet permits a backbone of plain viscose to be spun as a spine support for the carbon-loaded portion of the monofilament to give it added strength. The diameters of the dry, nondusting monofils can be varied greatly. For air cleaning purposes the nonfilanients range from 1/64 to 3/64 in. in diameter. Although imbedded in cellulose, the carbon's capxity to remove malodors remains high. In addition, when made into a filter unit, the resistance to air flow through the unit is low. The novel use of regenerated cellulose as a carrier for large quantities of activated carbon indicatcs that other materials (catalysts, ion exchange resins, etc.) can be similarly bound in cellulose and still retain a high level of their original performance.
    Additional Material: 6 Ill.
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