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  • 2020-2023
  • 1965-1969  (288)
  • 1945-1949
  • 1968  (288)
  • Chemistry  (230)
  • Polymer and Materials Science  (149)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 363 (1968), S. 207-212 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Es wurden Zn- und Cd-Komplexe mit den Liganden o-Carboxyphenyl-dimethylarsin, o-Carboxyphenyl-diphenylarsin und o-Carboxyphenyl-di(p-tolyl)-arsin dargestellt. Cd ergibt mit allen drei Liganden polymere, offenbar oktaedrische Komplexe der allgemeinen Zusammensetzung M(OOC·C6H4·AsR2)2, während dies beim Zink nur bei den beiden beiden letzteren Liganden der Fall ist. Mit dem Dimethylarsin bildet Zink einen Komplex Zn(OOC·C6H4)·AsMe2·Me2As·C6 H4COOH mit Fünferkoordination.
    Notes: The complexes of zinc(II) and cadmium(II) have been prepared with the ligands o-carboxyphenyldimethylarsine, o-carboxyphenyldiphenylarsine and o-carboxyphenyldi(p-tolyl) arsine. The complexes of cadmium(II) with all the ligands and that of zinc(II) with the latter two have been assigned the general formula M(OOC·C6H4·AsR2)2 and appear to be octahedral due to their polymeric nature. Zinc(II) forms complex, Zn(OOC·C6H4·AsMe2)2·Me2 As·C6H4COOH, with the first ligand which is pentacoordinated.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 909-918 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of styrene has been carried out with VCl4-AlEt3 and VCl4-Al(i-Bu)3 catalyst systems. These two systems have been found to behave in a similar manner but their behavior is different from those systems where VOCl3 has been used instead of VCl4. Reaction is first order with respect to monomer concentration for both the systems and first order with respect to catalyst in the case of VCl4-AlEt3. In the case of VCl4-Al(i-Bu)3, the rate of polymerization is independent of catalyst concentration but intrinsic viscosities increase with increasing catalyst concentration. The average valence of vanadium in the catalyst complexes has been discussed in relation to nature of catalyst sites. Activation energy and effect of diethyl zinc support the anionic mechanism for the two systems.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When cellulose triacetates and some hydrolyzed acetates are boiled in 2.5N hydrochloric acid there is no residue. Under the same conditions cellulose is hydrolyzed, and a residue is obtained with a limiting viscosity that is related to the average length of the cellulose crystallites. These findings are combined to develop a method for studying the progress of acetylation through the amorphous portion of cellulose and into the crystallites, and to investigate the relative reactivities of cellulose I and cellulose II. Acetates were made from cotton and wood cellulose by a “fibrous” (heterogeneous) esterification involving sulfoacetic acid or perchloric acid catalyst in acetic acid-acetic anhydride; the final acetyl contents (10-41%) were attained by stopping the reaction at various points short of the triester (rather than by hydrolyzing a triester). When these acetates were boiled in 2.5N HCI they did not disappear completely, and the residues were cellulose I, indicating that cellulose acetate had been removed. With increasing acetyl the yield of residue decreased, and beyond about 33% acetyl the viscosity and x-ray measurements showed that the length and width of the crystallites decreased. However, when a nonsolvent such as toluene was added to the acetylation medium, the limiting viscosity did not change over the same acetyl range (up to 40%). Samples of varying acetyl values were taken during a regular acetylation of cotton linters in a mixer with sulfuric acid catalyst. X-ray studies of the residues obtained by boiling the acetates in 2.5N HCI revealed the presence of unreacted cellulose I even after 40% acetyl had been reached. This explains why the manufacture of cellulose esters from cellulose I requires complete esterification before they are hydrolyzed to the desired acetyl level. It was shown that there is a distinct difference between the acetylation reactivity of cellulose I and cellulose II. This indicates the importance of avoiding cellulose II formation during the refinement of cellulose for the manufacture of cellulose acetate in a process involving activation with acetic acid.
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 849-860 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Precise heat capacity values are reported over the temperature range from 10 to 360°K. for a sample of atactic polystyrene having a narrow molecular weight distribution. This sample was taken from the stock from which National Bureau of Standards Standard Sample 705, Narrow Molecular Weight Distribution Polystyrene, was established. Data are reported for the sample as received, and after an annealing procedure. At temperatures below about 60°K. a systematic difference comparable with the limits of experimental precision appears between the values obtained for the present sample as received and after the annealing, although at higher temperatures the values for the two conditions showed no systematic difference beyond the limits of precision of the measurements. At temperatures above 100°K., previously published values for atactic polystyrene samples of various molecular weight distributions and for isotactic polystyrene agree within about 0.5% of the values from this investigation. At temperatures below 100°K. significant heat capacity differences appear, especially between values for the atactic and the isotactic isomers, and even between atactic samples of different molecular weight distribution.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 1435-1449 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Decay reactions of the free radicals produced in irradiated polyethylene (high-density and low-density materials) were examined in connection with the molecular motion of the matrix polymer. Three temperature regions, in which the free radicals decay very rapidly, at around 120, 200, and 250°K, were designated TA, TL, and TB, respectively. The decay of the free radicals at these temperatures had activation energies in high-density polyethylene of 0.4 kcal/mole for TA, 9.4 kcal/mole for TL, and 18.4 kcal/mole for TB. In low-density polyethylene these quantities were 0.7 kcal/mole for TA, 23.1 kcal/mole for TL, and 24.8 kcal/mole for TB. Comparison of time constants for the decay reactions and for molecular motion of the matrix polymer indicate that the decay in TA and TB is closely related to molecular motion in the amorphous regions of the polymer. The decay of the free radicals at TL in high-density polyethylene is due to molecular motion associated with local mode relaxation at lamellar surfaces, while that of low-density polyethylene is due to local mode relaxation in the completely amorphous region. Steric configurations of the free radicals which decay in the respective temperature regions were also investigated.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 509-525 
    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 a systematic study of the elution column fractionation of a well characterized branched polyethylene sample it was found that one of the most important factors contributing to the efficiency was the composition selected for the p-xylene-butyl cellosolve eluting mixture. With a mixture representing the critical solvent composition at 126°C., as determined by cloud point measurements, and deposition to an amorphous phase on a fine sand support, viscosity-distribution curves were obtained which were highly reproducible and completely free of any reversal. No further improvement was gained by using an elution temperature other than 126°C. or by the substitution of tetralin or mesitylene for p-xylene. Precipitation down a temperature gradient to produce a physical separation of species provided enhanced fractionation but is of doubtful practical interest. Fractionation was readily scaled up from 2g. to 4 or 6g., merely by increasing the mixing vessel size from 500 cc. to 1000 cc. There was no loss of efficiency, and fractions with M̄w = 8 × 106, more than twentyfold higher than the sample value, were obtained despite eluted polymer concentrations exceeding 0.2%. There is evidence that many of the expected differences in the fractionation behavior of linear and branched polyethylene are erased when a solvent mixture is used which has been adjusted to the appropriate critical composition.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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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: Fractions from several elution column runs on samples of up to 6 g. of a well-characterized high-pressure polyethylene were analyzed by absolute molecular weight methods and several other techniques. The Mn and Mw integral distribution curves are free from any reversal, as was the viscosity distribution curve. Fractions with Mw as high as 8 × 106 were recovered, more than 20 times higher than the original sample's Mw. The polydispersity of the fractions increases from Mw/Mn = 1.5 or less in the low molecular weight fractions to a nearly constant value of 4.5-5.0 in fractions above 60% cumulative sample weight. Nonetheless, refractionation on the elution column shows that the fractions are narrowly distributed in terms of solubility, while GPC analysis reveals that the fractions have an extremely narrow size distribution. It is concluded from the combined results that long-chain branching plays an important role in determining the equilibrium solubility and, further, that long-chain branching increases the polymer solubility. Sample calculations are provided, which illustrate the effect of fraction polydispersity on calculated original sample molecular weights and the fit of the fractionation results to several model distribution functions.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 2033-2038 
    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: Expressions were derived relating changes of intrinsic viscosity to reaction time, based on a scheme previously presented for the uncatalyzed, uninhibited thermal oxidation of polyolefins. A value of the kinetic parameter A may be obtained from these expressions by using an iterative type of procedure and employing data presented by other workers for the oxidation of atactic polybutene-1. This value of A was compared with the corresponding value obtained by the authors from rate of carbonyl formation studies in oxidation of atactic polybutene-1 by means of infrared absorption spectroscopy methods. The good agreement between the values of A obtained from the two different experimental techniques employed lends further support to the validity of the scheme used and the expressions derived therefrom.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 38 (1968), S. 301-304 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the physicochemical properties like refractive index, spectrophotometry, conductivity and pH measurements of a series of mixed solutions of uranyl nitrate and mercurous nitrate have shown the existence of two complexes in solution in the (1:1) and (1:2) molecular ratios respectively viz. \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm UO}_2 \left({{\rm NO}_3 } \right)_2 \cdot {\rm Hg}_2 \left({{\rm NO}_3 } \right)_2,} \hfill & {\left({\rm i} \right)} \hfill \\ {{\rm UO}_2 \left({{\rm NO}_3 } \right)_2 \cdot 2{\rm Hg}_2 \left({{\rm NO}_3 } \right)_2,} \hfill & {\left({{\rm ii}} \right)} \hfill \end{array} $$\end{document}Both the above mentioned compounds have been detected only in the solution by the breaks in the usual curves when various properties like conductivity, refractive index, spectrophotometry and pH were plotted against the m.l. of mercuric nitrate (M/10) added to a fixed volume of uranyl nitrate (M/10).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 2 (1968), S. 443-446 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Acetylcholine esterase and the glucose oxidase-peroxidase systems have been entrapped in Silastic matrices. The entrapped acetylcholine esterase exhibited remarkable stability as compared to the free enzyme in solution. The glucose oxidase-peroxidase system indicated that consecutive reactions may be carried out by several enzymes entrapped within a single matrix. The effect of various inorganic materials on the entrapped enzymes was also investigated.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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