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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 92 (1988), S. 2663-2668 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 8248-8253 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 2694-2698 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 91 (1987), S. 3910-3914 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 30 (1993), S. 579-586 
    ISSN: 1436-2449
    Keywords: polystyrene ; hydrodynamic ; excluded volume ; binary solvents ; viscosity ; θ-condition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract At 298 K, intrinsic viscosity [η], has been measured for fifteen polystyrene, PS, samples of different relative molar masses M in pure toluene T, and seven different binary solvents. These solvents were toluene / methanol (MeOH) mixtures having different volume fractions of MeOH. The θ-composition for the binary solvent system was found to be 77% T / 23% MeOH at 298 K. The dependance of excluded volume of polymer molecules on M and the solvation power was demonstrated. A constant value of 0.633 nm for the effective unit length, b, was obtained under θ-condition. Meanwhile a non-constancy of b, obtained in case of thermodynamically good solvents, was attributed to the neglect of excluded volume effect.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract At 298.15K, intrinsic viscosity [η] has been measured for poly (vinylpyrrolidone), PVP, samples of different relative molar masses M in pure water and eight different binary solvents. These solvents were water/acetone mixtures having different volume fractions of acetone (ACT). The solvation power of these mixtures showed a cosolvancy effect. The maximum solvation power was found for the mixture containing 0.2 volume fraction of ACT. The value of Kθ=74×10-3 dm3kg-1 was utilized for calculating the unperturbed dimensions, u.d., steric factor, σ, the characteristic ratio, C∞, and the persistence length, ap. Values of 0.666 Ao, 2.28, 10.38 and 8.76 Ao, respectively, were obtained for PVP in theta-solvent. The calculated values of the effective radius (Re), effective unit length (b) and the effective hydrodynamic radius of monomeric unit (ro) showed the complete impermeability of polymer molecules. Some errors in the polymer handbook and CRC, water-soluble synthetic polymers, were demonstrated with its logical corrections.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary An ethylenically dibasic acid amide was prepared by reacting anthranilic acid with maleic anhydride and characterized by various methods. The unsaturated dibasic acid amide was used for preparing three novel unsaturated polyesters with ethylene glycol (EG), diethylene glycol (DG) and tetraethylene glycol (TG), respectively. The molecular weights of the prepared polyesters were determined by the end group analysis. These polyesters were diluted with styrene / acrylonitrile (AN) mixture to prepare curable resins with inhibited premature gelation. The effect of the structure of the resins on their curing behavior and mechanical properties has been investigated.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 35 (1995), S. 229-236 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary A series of unsaturated polyesters (UP) based on phthalic anhydride (PHA), succinic acid (SU), adipic acid (AD), sebacic acid (SE), maleic anhydride (MA), ethylene glycol (EG), diethylene glycol (DG), triethylene glycol (TG), and styrene (Sty) were prepared. The molecular weights of the prepared polyesters were determined by the end group analysis. The effect of the structure of the resin on its mechanical and curing behavior has been investigated. On the basis of the experimental study, we concluded: (1) the maximum curing temperature, Tmax, is related to the molecular weight of the glycol incorporated in these castings. In this context, Tmax was found to decrease with increasing the molecular weight. Meanwhile, the time to peak temperature, tmax, was increasing; (2) the values of Tmax, Young's modulus and compressive strength were found to be influenced to a large extent with the type of the saturated acid as well as the molecular weight of the glycol embodied in these resins. A relation representing the variation of compressive strength, σu, as a function of equivalent polymerizable double bonds, EPDB, was derived. It was assumed that this equation can be used to predict the compressive strength for any particular UP formula from its theoretical EPDB value.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 15 (1994), S. 183-188 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 195 (1994), S. 159-166 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: For solutions of polystyrene (PS) samples of different relative molecular mass (molecular weight) M and intrinsic viscosities [n] have been measured at 298,15 K in pure toluene (T) and toluene/methanol (MeOH) mixtures. Upon mixing toluene (good solvent (1)) and methanol (nonsolvent (2)), a systematic decrease in the solvation power was obtained. A critical examination of the Stockmayer-Fixman method for obtaining unperturbed dimensions from intrinsic viscosity measurements has been made. It was found that the unperturbed dimensions were not constant and different from those measured in a theta solvent (T/MeOH mixture having volume fraction of methanol (φMeOH) = 0,23). The derived values of unperturbed dimensions were found to increase with increasing Kuhn-Mark-Houwink-Sakurada exponent a. A modified form of the Stockmayer-Fixman equation is presented. It is suggested that the volume effect be taken into account in a complementary fashion to obtain accurate estimates of unperturbed dimensions from data in active solvents where the mean-square end-to-end distance 〈r2〉 increases at these conditions more rapidly than M. Different viscosity measurements of polystyrene (PS) and poly(N-vinyl-2-pyrrolidone) solutions containing non-ideal solvents were taken from the literature and found that the newly proposed, though purely empirical equation is valid.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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