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  • Polymer and Materials Science  (27)
  • Engineering  (10)
  • Crosslinking  (3)
  • Oryza sativa  (3)
  • 11
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 75-85 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new route to prepare optically active polyamides was established, based on the polycondensation of two new active diesters: the active diesters of 4-chloro-1 hydroxybenzotriazole, such as 1,1'-(terephthaloyldioxy)bis(4-chloro-benzotriazole), and 1,1'-(isophthaloyldioxy)bis(4-chlorobenzotriazole), with optically active isomers of 2,4-diaminopentane. Dipolar aprotic solvents such as N,N-dimethylformamide and dimethyl sulfoxide were used as reaction solvents. The solution polycondensation carried out in solution at room temperature afforded optically active polyamides. The aminolysis of the two active diesters was carried out as a model reaction study.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 167-171 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 389-403 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polynucleotide analogs consisting of poly(vinylamine) as the backbone and optically active thymine and adenine derivatives as the pendants were synthesized. The pendants were prepared by the addition reaction of the nucleic acid base to ethyl crotonate followed by hydrolysis. The pendants were resolved using brucine as the resolving agent and an acetone-water mixture as the fractional crystallization solvent. The active esters of the pendants also were prepared. Poly(vinylamine) was isolated from water employing a weak acid, N-hydroxysuccinimide (HOSu), to protect the amino group of the poly(vinylamine). Model reactions for grafting were examined. Grafting reactions were carried out by reacting the active esters with the PVAm.6HOSu complex at room temperature.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1539-1547 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photochemical polymerization rates of isoprene, ethyl methacrylate, and of styrene in various aromatic solvents were measured. The average lifetimes of propagating radicals were measured by the rotating sector method. The polymerization rate constants, Kp, were determined and compared with dipole moments (μ) and Hammett σ constants for the aromatic solvents. Linear correlations of log(kp/kp, benzene) vs. μ and σ were obtained.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 373-388 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polynucleotide analogs with a polyethylenimine backbone and optically active thymine- and adenine-containing pendants and their model compounds were synthesized. The pendants were prepared by the addition reaction of the nucleic acid base to ethyl crotonate. The ammonium salt of 3-(adenin-9-yl)butyric acid was employed to replace its free acid for the formation of diastereomeric salt with brucine. Fractional crystallization of the diastereomeric salt generates the partially resolved enantiomers. The solubility difference between the racemic mixture and its enantiomer was utilized to obtain the pure enantiomers. The active esters of the pendants were prepared. Grafting reactions were carried out by the reaction of active esters with PEI at room temperature. Completely grafted polymers were obtained.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 503-521 
    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 deformation and fracture characteristics of ABS have been investigated under tension, compression, and tension-compression fatigue cycling. The behavior of the rubber-modified polymer is compared with that of unmodified styrene-acrylonitrile, copolymer. The dispersed rubber particles in ABC cause extensive plastic deformation of the matrix material, markedly reduce the compressive yield stress, and, under tensile loading, cause yielding rather than early fracture. Under alternating stress conditions crazes occur sooner and lead to earlier craze breakdown, crack development, and reduced lifetime to fracture. The influence of rate of loading has been studied under applied tension and under fatigue cycling. The tensile yield stress varies linearly with the log of the strain rate in accord with the Eyring rate equation and, from the measured slope, the activation volume is estimated to be 2.2 nm3. The time to fatigue fracture reduces significantly with increasing frequency while cycles to fracture increase at a modest rate. Fatigue failure in ABS is not a cycle-dependent process, nor is it in accord with a damage accumulation model, but it more nearly resembles the former. The influence of a dispersed rubber phase, and of loading rate, on fracture surface morphology is discussed.
    Additional Material: 14 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 1573-1588 
    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: A unique series of ethylene and propylene sequential polymerization experiments have been carried out in a stirred bed gas phase reactor using unsupported Stauffer AA catalyst (TiCl3· \documentclass{article}\pagestyle{empty}\begin{document}$\frac{1}{3}$\end{document}AlCl3). Several interesting kinetic results were observed. It was found that propylene causes rate enhancement for a subsequent ethylene polymerization but that ethylene causes a rate reduction for a subsequent propylene polymerization. Furthermore, the rate enhancement/reduction effect increases with the duration of the preceding polymerization. Chemical/kinetic effects were found to be the likely causes of both the rate enhancements and the rate reductions observed during sequential polymerization. It was also shown that enhanced monomer sorption caused by the presence of a more soluble component, such as a heavier comonomer, does contribute to rate enhancement during simultaneous copolymerizations, but is not a factor for sequential polymerizations. © 1993 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 1101-1105 
    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 major contributors to the compounding energy of a poly(vinyl chloride) (PVC) sample in the Haake torque rheometer are starting temperature, rotor speed, and totalized torque. In this study, the compounding energy was calculated by using an energy balance in the internal mixer reported by Pedersen. The fusion levels of the PVC samples, which were prepared in the Haake torque rheometer at various blending conditions (starting temperature = variable, rotor speed = 60 rpm, and totalized torque = 10 kg-m-min), were determined by DSC and a capillary rheometer. The compounding energy was then correlated with the fusion level. The simple total energy balance can be applied to correlate the compounding energy with the fusion level of the PVC compound prepared in the Haake torque rheometer. © 1995 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 1107-1115 
    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: Poly(vinyl chloride) (PVC), PVC/chlorinated polyethylene (CPE), PVC/oxidized polyethylene (OPE), and PVC/CPE/OPE compounds were prepared in a Haake torque rheometer at various temperatures, rotor speeds, and totalized torques (TTQ). The fusion characteristics of these PVC compounds (fusion time, fusion torque, and fusion temperature) were studied. Longer fusion time results in higher fusion temperature. Higher fusion temperature results in lower fusion torque. The fusion time of PVC/OPE compounds is the longest among these PVC blends. However, the fusion time of PVC/CPE/OPE compounds is the shortest among these PVC blends. The fusion time of the PVC/CPE/OPE compound is significantly different from those of PVC, PVC/OPE, and PVC/CPE compounds at the medium starting temperature and the medium rotor speed. Scanning electron microscopy (SEM) analyses successfully revealed the surface morphological changes of the fusion of PVC, PVC/OPE, PVC/CPE, and PVC/CPE/OPE compounds. The lubrication mechanisms of these PVC compounds have also been postulated. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 1087-1091 
    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: Chlorinated polyethylene (CPE) is a commonly used impact modifier of poly(vinyl chloride) (PVC). The major goal of this research was to understand the fundamental morphological aspects of PVC/CPE blends. Scanning electron microscopy (SEM) was used to image the surface structure of these blends, and both transmission electron microscopy (TEM) and scanning-transmission electron microscopy (S-TEM) were used to image the morphological boundaries of the blends. TEM imaging distinguishes the boundaries between PVC and CPE more clearly or better than does S-TEM, but it is time-consuming. However, some CPE particles are not observed in TEM because of inefficient staining. S-TEM imaging is much faster and does not depend on staining for the imaging of the CPE phase. © 1995 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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