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  • Chemistry  (32)
  • Computer Systems
  • 1980-1984  (26)
  • 1975-1979  (5)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 19 (1980), S. 1555-1566 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Possible conformations of lacto-N-tetraose, lacto-N-neotetraose, related disaccharides, and other milk oligosaccharides have been studied by an energy-minimization procedure using empirical potential functions. Lacto-N-tetraose favors a “curved” conformation, while lacto-N-neotetraose favors an approximately “straight” conformation. These two conformations differ mainly in the position of the terminal galactose residue with respect to the rest of the molecule. This difference explains the greater strength of lacto-N-neotetraose compared with lacto-N-tetraose in its ability to inhibit the cross-reaction of blood group P1 fractions with Type XIV pneumococcal antipolysaccharide. Although the favored conformation of lacto-N-tetraose (inactive) agrees with the model proposed by the earlier workers, that for lacto-N-neotetraose (active) differs. The favored conformations for the disaccharides galactose-β(1-4)-N-acetylglucosamine, galactose-β(1-3)-N-acetylglucosamine, and lactose are similar in overall shape, differing only in the nature and orientation of the side groups. This explains their nearly equal inhibitory activity. These theoretical models also explain the increased activity of lacto-N-fucopentaose I over that of lacto-N-tetraose and the relative activities of the substituted lactoses. The present studies suggest that it is the overall shape of the molecule which is important for activity, rather than the terminal β(1-4)-linked galactose residue alone.
    Additional Material: 7 Ill.
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Aqueous polymerization of MMA was kinetically studied using separately two complexes of sulfur dioxide as initiators, namely, quinoline-sulfur dioxide (Q-SO2) complex and tetrahydrofuran-sulfur dioxide (THF-SO2) complex. In each case the initiator exponent was 0,5 and the monomer exponent was 1,5. Kinetic data, inhibitory effect of hydroquinone, and incorporation of sulfoxy end groups in the polymers indicate a radical mechanism of polymerization with first order dependence on monomer for the rate of initiation while termination appears to take place bimolecularly.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 179 (1978), S. 1209-1217 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studies on the relative efficiencies of 3d-transition metal oxides as catalysts for the polymerization of vinyl ethers revealed that V2O5 is the most efficient catalyst. Some kinetic studies with the system isobutyl vinyl ether/V2O5/benzene were carried out at ambient temperature. It was found that the rate is second order in isobutyl vinyl ether (IBVE) concentration (0,25 to 2,0mol.1-1) and the inhibition of the polymerization by pyridine suggests a cationic mechanism. Rp increases by the use of benzaldehyde along with V2O5, whereas water (3.10-3mol.1-1) seems to have no effect on Rp. Over the temperature range of 15 to 60°C, Rp as well as [η] attain a maximum value at about 32°C. [η] is unaffected by varying the amounts of oxides, whereas it increases with increasing IBVE concentration. No stereoregularity in the product polymer was observed by using V2O5 alone or in combination with modifiers such as benzaldehyde or carbon disulfide. The kinetics are interpreted in terms of the Hinshelwood-Langmuire mechanism assuming a single point adsorption.
    Additional Material: 6 Ill.
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was found that the Py-SO2 complex (4-140 mmol·1-1) initiates the photopolymerization of methyl methacrylate (MMA) in bulk at 40°C, the initiator exponent, kp2/kt, and the monomer exponent being 0,30, 1,27·10-2 1·mol-1·s-1, and 1,00, respectively. The radical generation is followed by an in-situ initiator-monomer complexation reaction. The kinetics of the photopolymerization of MMA were also studied using the (Py-SO2)-complex (0,01-0,35 mol·1-1) in redox combination with benzoyl peroxide (BZ2O2) (2 - 110 mmol·1-1) as initiator in the presence of variable concentrations of pyridine (1 - 7 mol·1-1). The initiation depends on the concentrations of all the reactants in the system, and the reaction order with respect to either component of the redox pair is equal to 0,5 or reasonably less than 0,5, depending on whether or not the initiating component in question is present in the system in excess compared to its counterpart in the redox combination. Variable monomer exponents, largely dependent on [BZ2O2], characterize the redox photopolymerization process. The monomer exponent value, unity at [BZ2O2] = 0, progressively decreases with increasing [BZ2O2] (non-ideal kinetics). The rate enhancing effect of the solvent pyridine is more prominent at higher [BZ2O2]. The kinetic nonidealities in each case were further analyzed and interpreted in terms of (a) primary radical termination and (b) degradative initiator transfer. Relative effects of the variation of the level of dilution with pyridine were also analyzed.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1629-1635 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Et2Zn in combination with POCl3 induces the cationic polymerization of isobutyl vinyl ether and N-vinyl carbazole at ambient temperature. The rate is directly proportional to [Et2Zn]. [POCl3] up to a mole ratio of unity of the components, and thereafter it decreases. At a fixed ratio of [Et2Zn]/[POCl3] the rate is second order in [Isobutyl vinyl ether]. Rate and [η] decrease in the presence of basic additives, pyridine, and water. Unlike the system Et3Al/POCl3, the present combination does not lead to any stereoregular poly(isobutyl vinyl ether) at ambient or lower temperatures. A cationic mechanism is proposed and an appropriate kinetic scheme is suggested.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 182 (1981), S. 261-264 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 1263-1271 
    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 influence of hydrofuramide (a reaction product of furfural and ammonia) on the network structure and overall kinetics of thiuram vulcanization of natural rubber is reported. The nature of the network structure of the thiuram vulcanizates in the presence and absence of hydrofuramide was determined using triphenyl phosphine (Ph3P) as a chemical probe. The presence of hydrofuramide produces structural complexity of the vulcanizate. The overall kinetics of thiuram vulcanization follows a first-order-rate law in the presence as well as in the absence of hydrofuramide. The rate constant increases while the energy of activation decreases in the presence of hydrofuramide.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 149-159 
    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: Crosslinked polymers based on the condensation of furfural with N-vinylcarbazole and poly(N-vinylcarbazole) were prepared. The effect of variation of furfural concentration on the condensation of furfural with N-vinylcarbazole and its polymer was studied. The polymers were chemically modified into phosphonic acid cation exchange resins. The effects of variation of AlCl3, PCl3, and furfural amounts, reaction time, and rephosphorylation on the synthesis and capacities of cation exchange resins were also studied.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 72 (1978), S. 57-66 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Poly(N-vinylcarbazol) wurde mit verschiedenen Reagenzien sulfoniert und die Ionenaustauschkapazität der erhaltenen Harze bestimmt. Eine maximale Kapazität von 4,5 meq · g-1 des trockenen Harzes wurde durch 10stündige Reaktion mit 98,8proz. H2SO4 bei 30°C erhalten. Die pH-Titrationskurven lassen einen starken monofunktionellen Kationenaustauscher mit einem pK-Wert von 2,2 erkennen. Das Harz zeigt eine mäßige Austauschgeschwindigkeit mit NaCl und ist bis zu 250°C thermisch stabil.
    Notes: Poly(N-vinyl carbazole) was sulfonated with different sulfonating agents and ion exchange capacities of the resins produced were evaluated. A maximum capacity of 4.5 meq · g-1 of dry resin was realized when sulfonation was done with 98.8% H2SO4 at 30°C for 10 h. The pH titration curves reveal the nature of a strong monofunctional cation exchanger with a pK value of 2.2. The resin exhibits a moderate rate of exchange with NaCl and is thermally stable up to ca. 250°C.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 73 (1978), S. 53-61 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Ein Kationenaustauscher wurde durch Kondensation von Polyisobutylvinyläther und Furfural hergestellt. Als Katalysator diente konzentrierte Schwefelsäure. Der Austauscher wurde durch Messen der Austauschkapazität, durch Untersuchen seiner thermischen Belastbarkeit und durch Bestimmen seines Verhaltens bei der pH-Titration charakterisiert. Es scheint sich um einen Austauscher mit schwachen Säregruppen zu handlen, die wohl als —COOH-Gruppen vorliegen und durch Oxidation aus den Furfuralgruppen entstanden sein dürften.
    Notes: A cation exchange resin was synthesized from the condensation product of poly(iso-butyl vinyl ether) and furfural by treating it with concentration sulphuric acid. The resin produced was characterized by measuring its total and salt splitting capacities, and by studying its thermal characteristics and behaviour to pH metric titration. The latter suggests the resin to be a weak one possibly containing —COOH groups, which result from the oxidation of the furfural aldehyde group by sulphuric acid.
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