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  • Polymer and Materials Science  (25)
  • Wiley-Blackwell  (25)
  • Wiley
  • 1995-1999  (16)
  • 1965-1969  (5)
  • 1960-1964  (4)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 1951-1962 
    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: Heterogeneous propionylation of cotton cellulose, in the form of yarn, was carried out by reaction with propionyl chloride, in a medium of pyridine and dimethylformamide (DMF). The product was a mixed propionate-α-propionylpropionate ester of DS varying from 0.24 to 2.94. The supramolecular structure of these esters was studied by kinetic analysis as well as by the measurements of density, refractive index, and x-ray diffraction. The Sakurada plot of DS against time of reaction showed a discontinuity at a DS of about 2.0, where the x-ray diffraction pattern shows almost complete loss of crystalline structure. The interpretation, based on the assumption that the Sakurada curve actually represents the sum of two simultaneous rate processes acting in the amorphous phase and at the crystalline surfaces, seems to explain the data adequately. The density showed a continuous decrease, consistent with the idea of continuous destruction of crystalline structure with progressive substitution. Refractive indices showed a continuous decrease with substitution and birefringence was almost absent at complete substitution. The calculated value of molar refraction for the sample of DS 2.94 agreed closely with the experimentally observed value. The x-ray diffraction intensity traces gave convincing evidence of the progressive decrystallization of cellulose with the degree of substitution. Decrystallization seems to be more or less complete at about a DS of 2.0.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1995-1999 
    ISSN: 0887-624X
    Keywords: poly-γ-D-glutamic acid ; biopolymer ; covalent modification ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methods for the covalent modification in aqueous solution of poly-γ-D-glutamic acid from Bacillus licheniformis have been studied. Co-derivatization of a synthetic UV-absorbent amine and ethanolamine, using a water-soluble carbodi-imide coupling agent, yielded a water-soluble modified polymer. Derivatization of the polymer was accompanied by cleavage of the γ-linked polypeptide backbone, and a reduction in molecular mass from 170 to 10 kDa. A procedure was developed for the removal of noncovalently bound ligands by treatment with 5 M CaCl2. The polymer sidechains also reacted in aqueous solution with p-nitrophenyl acetate to form covalent linkages. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 1995-1999, 1998
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2469-2478 
    ISSN: 0887-624X
    Keywords: Bismaleimide ; BDS ; allylamine ; high temperature resins ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of 3,3′-bismaleimidodiphenylsulphone/allylamine (3,3′-BDS/A) adducts were prepared by reacting 3,3′-BDS with various molar percentages of allylamine (A). The reaction path, revealed by a model compound study of n-phenylmaleimide reacting with allylamine, indicates that the imido ring of 3,3′-BDS was opened by allylamine resulting in the formation of two amido groups. The infrared and mass spectra of curing 3,3′-BDS/A adducts indicate that the allylamino groups cleaved with the recovery of imido ring of 3,3′-BDS and then participated in the cure reactions. The cure reaction paths depend on the amount of allylamino groups in the 3,3′-BDS/A adducts. When it is in a small amount, the cleaved allylamines will accelerate the homopolymerization of 3,3′-BDS through the maleimide double bonds. When allylamino groups are plentiful, the cleaved allylamines might polymerize by themselves through the allyl groups. A decomposition mechanism of 3,3′-BDS/A adducts was suggested by mass spectra. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2469-2478, 1997
    Additional Material: 12 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Advanced Materials 8 (1996), S. 850-852 
    ISSN: 0935-9648
    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: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 1 (1963), S. 231-238 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies of different preparations of ribonuclease A by thin film dialysis and countercurrent distribution have shown the existence of conformational isomers. These forms are slowly interconvertible in a particular solvent environment. They show the minimum molecular weight of ribonuclease and do not differ enzymatically or by rotatory dispersion.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 1009-1016 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of novel quinoxaline-based conjugated polymers which contain a ruthenium(II) bipyridine complex were synthesized by the Suzuki coupling reactions. UV/VIS spectroscopy showed that the spectral features of the polymers are dependent on the amount of metal complex present. Results from excitation and emission spectroscopy suggest an energy transfer between the backbone and the metal complex. The polymers exhibit hole carrier mobilities of ≈ 10-5 cm2 · V-1 · s-1, which is comparable to organic photoconductors.
    Additional Material: 4 Ill.
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  • 7
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of N-methyl-2-pyrrolidinone (NMP) as solvent on the polymerization reactions of 1,3-bis(4-chlorobenzoyl)benzene (1,3-CBB) and 1,3-bis(4-fluorobenzoyl)benzene (1,3-FBB) with 4,4′-isopropylidenediphenol (bisphenol-A) were examined. The failure of these reactions to produce high molecular weight polymers in the presence of anhydrous potassium carbonate is due to dehalogenation of 1,3-CBB via substitution radical-nucleophilic unimolecular (SRN1) processes. On the other hand, 1,3-FBB undergoes nucleophilic aromatic substitution reactions (SNAR) with the carbonate anion at elevated temperatures. However, it is possible to synthesize high molecular weight polymers from 1,3-FBB and bisphenol-A in NMP either by first forming the bisphenoxide with stoichiometric amounts of aqueous sodium hydroxide or in the presence of anhydrous potassium carbonate at a lower reaction temperature.
    Additional Material: 3 Ill.
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  • 8
    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: Two reaction paths which can be followed when an acid chloride reacts with an alcohol are discussed. The role of pyridine as solvent and catalyst in this reaction is described. The importance of inductive and resonance effects and the size and arrangement of groups near the carbonyl are emphasized. The heterogeneous preparations of seven cellulose partial esters, the phenylacetate, benzoate, trimethylacetate, triphenylacetate, β,β,β-triphenylpropionate, α-(4-biphenylyl)phenylacetate, and mesitoate are described. Pronounced interference with esterification is noted only in the preparation of the triphenylacetate. Steric hindrance and a poor ability to ionize are considered to be responsible for this result. Outstanding resistance to saponification, thought to be the result of steric hindrance and a reduced tendency to ionize, is reported for three of the cellulose esters, the triphenylacetate, the β,β,β-triphenylpropionate, and the mesitoate.
    Additional Material: 3 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 337-354 
    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: Polyfunctional alcohols, acyclic, cyclic, and heterocyclic imines, and organotin oxides have been studied as crosslinking agents for chlorosulfonated polyethylene. Mechanisms for the crosslinking reactions involving the sulfonyl chloride moiety have been proposed. Differences in curing activity have been correlated with structural modifications of the curing agents consistent with classical chemical reactions for nonpolymeric systems. Of the curing systems examined, the polyols provide nontoxic, low cost, safe-processing formulations offering excellent physical properties which have found use in practical commercial applications.
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1191-1201 
    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: Isotherms have been obtained for the absorption of water by proteins and polyamides and by simple amides closely related to the repeat chemical unit of the polymers. The differential heat of absorption of water at zero water content has also been determined for these substances, from isosteres and from heats of mixing. In addition the nature of the hydrogen bonding of water to these compounds has been investigated by infrared spectroscopic methods. The large differences found between the heats of absorption by the polymers and the simple model compounds are discussed.
    Additional Material: 7 Ill.
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