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  • Polymer and Materials Science  (3)
  • Porcellio laevis  (3)
  • hepatopancreas  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part A: Physiology 48 (1974), S. 375-385 
    ISSN: 0300-9629
    Keywords: Isopoda ; Phosphomonoesterases ; Porcellio laevis ; Porcellionidae ; acid phosphatase ; alkaline phosphatase ; exoskeleton ; gonads ; gut regions ; hepatopancreas ; histochemical distribution ; mitochondria ; nuclei
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part B: Biochemistry and 47 (1974), S. 307-316 
    ISSN: 0305-0491
    Keywords: Isopoda ; Porcellio laevis ; Porcellionidae ; active centre ; alkaline phosphatase ; cellulose acetate electrophoresis ; effect of amino acids ; energy of activation ; enzyme subunits ; heavy metal inhibitors ; heterogeneity ; inhibition by l-phenylalanine
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part B: Biochemistry and 45 (1973), S. 911-921 
    ISSN: 0305-0491
    Keywords: Phosphomonoesterases ; Porcellio laevis ; acid phosphatase ; alimentary canal ; alkaline phosphatase ; hepatopancreas
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 617-625 
    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 diffusion coefficient at zero penetrant concentration D0 of dichloromethane, chloroform, carbon tetrachloride, cyclohexane, benzene, o-xylene, m-xylene, and p-xylene, and n-hexane in LDPE were measured at 25°C, using the desorption method. The D0 values obtained in this way are correlated with the size, shape, and chemical nature of the penetrant molecules. The temperature dependence of the diffusion coefficients of toluene and n-hexane in LDPE are also reported in the limited temperature range of 25-45°C. It indicates that, in spite of a size larger than that of toluene, n-hexane has a lower activation energy of diffusion.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 38 (1989), S. 1503-1514 
    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 diffusion coefficients at zero penetrant concentration, D0, of n-heptane, n-heptane, n-octane, n-decane, and 2,2,4-trimethylpentane (TMP) in LDPE were obtained in the range of 25-50°C, using the desorption method. The dependence of D0 on the size and shape of the penetrant is reported. It was found that D0 decreases with increasing penetrant molecule size. The activation energies of diffusion in the temperature range of 25-50°C increase with increasing penetrant molecule size and are independent of temperature. The results are interpreted in terms of the free volume theory and semiquantitative estimates of the free volume parameters are reported.
    Additional Material: 5 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 39 (1990), S. 655-678 
    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: Polystyrene (PS) and polyethylene (PE), along with their reactive counterparts, i.e., polystyrene having oxazoline reactive groups (OPS) and polyethylene with carboxylic acid groups (CPE), were melt blended in a Rheomix mixer. These blends were prepared by mixing these polymers in various proportions under a variety of conditions. In an alternate procedure the OPS, CPE graft polymer (OPS-g-CPE) was prepared by melt blending these two polymers beforehand, and subsequently this grafted polymer was used as a compatibilizer for PS-PE blends. The effects of the addition of OPS and CPE, on the one hand, and OPS-g-CPE, on the other hand, on the compatibility of PS-PE blends were investigated. The morphology of these blends was examined with a scanning electron microscope (SEM) and related to their tensile properties. The PS-PE blends are found to have the typical coarse morphology of incompatible blends and poor tensile properties while their reactive counterparts, OPS-CPE blends, have fine grain microstructure and show improved tensile strength throughout the range and improved elongation in the PE-rich blends. Relatively low concentrations of the reactive pair, oxazoline and carboxylic acid, are shown to be necessary to produce improved compatibility. The preblended graft copolymer OPS-g-CPE imparts compatibility to PS-PE blends also but not as effectively. This suggests that the addition of OPS and CPE during melt mixing of PS and PE forms OPS-g-CPE polymer at the interface and that these ingredients act as “in situ reactive compatibilizers” which improve physical properties.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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