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  • Articles  (14,436)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 6 (1972), S. 179-250 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 22 Ill.
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  • 2
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 18 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 1-14 
    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 radiation-induced graft copolymerization of styrene and various kraft softwood lignins was studied. Expression of the results as the usual “per cent graft” was impossible, because grafting caused the lignin to become extractable in solvents for the styrene homopolymer. However, evaluation of the effects of various solvents on the degree of reaction was made through an indirect, and possibly more characteristic, measure. Grafting was least pronounced under conditions of low lignin accessibility (e.g., when less than 10% methanol was present), but increased with the addition of better lignin solvents or with higher methanol concentrations. The precipitating nature of the latter conditions was also found to contribute to an accelerated rate of grafting. Surprisingly, the graft copolymer was found to degrade at higher doses. Proof of grafting is offered in a fractionation scheme. Measurement of the molecular weight of the polystyrene separated from the lignin backbone allows the estimation of approximately one polystyrene graft per lignin molecule in benzene-extractable copolymers. Two glass transition temperatures could be detected in several fractionated copolymers.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 61-68 
    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: Color stability in irradiated PVC may be achieved by (1) structural modification to block dehydrochlorination, (2) addition of radiation protectors, or (3) addition of radical scavengers. This study explores the latter approaches. Twenty-six compounds representing a variety of structural types were screened for their effectiveness as measured by subsequent color development. Fifteen of the compounds imparted partial or complete postirradiation stability. Possible stabilizer mechanisms are discussed.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 83-97 
    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 ultraviolet degradation of poly(vinyl chloride) films was studied in a photoreactor which supplied energy near 3000 Å. It was noted that the rate of degradation and color development was increased when the level of residual solvent in the cast films was increased. Two solvents were employed in the study: tetrahydrofuran and dichloroethane. The amount of residual solvent was correlated with the height of a characteristic peak at 2800 Å for tetrahydrofuran and 1900 Å for dichloroethane. Films which had very small traces of solvent showed excellent resistance to ultraviolet degradation, even in the absence of ultraviolet stabilizers. The analysis of solubility data showed that chain scission was controlling in the early stages of exposure, while crosslinking was controlling at later stages. As a result, it was not possible to apply Charlesby's treatment of radiation-induced degradation. Comparison with the results obtained by other workers for degradation at 2537 Å showed that degradation at this wavelength was much faster than degradation at 3000 Å. Furthermore, degradation at 2537 Å appeared to be controlled by crosslinking at all stages of exposure.
    Additional Material: 13 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 139-155 
    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: In this paper we define a new structural parameter of polymers, and show how this may be employed. This parameter, for which only the structure and the density are needed, is the relative number of network bonds per unit volume; it is written Ner (basis 1 cm3), and it is used in conjunction with the average connectivity or connection number CN of the network atoms, where the word connection also refers only to network bonds. The relationship of these two numbers makes it possible to present a unified picture of all polymers, organic and inorganic, including such highly condensed networks as diamond. By plotting Ner against CN, the region in which inorganic and organic polymers occur can be seen. This is called the polymer zone, and it is evident that carbon polymers occupy only a small part of it. From this graph, an arbitrary measure of bond packing efficiency can be deduced for carbon polymers. In addition, the process of graphitization and carbonization can be followed graphically within the polymer zone. Ner is also related to certain physical properties such as bulk modulus, hardness, and cubical coefficient of expansion, which depend (among other things) on the tightness of bond arrangement. The resultant correlations can be used to predict the value of Ner required to achieve given values of these properties for the more rigid structures.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 191-202 
    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(ethylene terephthalate) has been irradiated with UV light of different wavelengths and in various atmospheres. The extent of degradation was monitored by measuring the tensile strength, molecular weight, carboxylic acid endgroups, and fluorescence emission of the polymer. The importance of wavelengths 〈315 nm in causing deterioration was demonstrated to be mainly due to strong surface absorption which results in surface crazing and ultimate fracture under stress. Irradiation in nitrogen and under vacuum were found to give similar results, but with oxygen present in the system several significant differences were observed. In nonoxidative irradiations, crosslinking and discoloration of the polymer occurred. Under oxidative conditions, chain scissions and fluorescent material build-up resulted, whereas no crosslinking and only slight discoloration was observed. The possibility of a photo-oxidation reaction has thus been suggested, involving hydroperoxide formation, to explain the discrepancy in results obtained for the two types of environments.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 345-352 
    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 preparation of 3,3′-dichloro-5,5′-diaminobenzidine and its polymeric reaction products with pyromellitic dianhydride and 3,4,3′,4′-benzophenonetetracarboxylic dianhydride are described. The soluble amine-acid-amide form of the polymer is stable at higher concentrations than the corresponding polymers from 3,3′-diaminobenzidine or 3,3′,4,4′-tetraaminodiphenyl ether. Infrared spectra indicate that polybenzimidazopyrrolone structure is formed after cure. The preparation and properties of films and glass-reinforced laminates prepared from the polymers are described.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 395-406 
    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 variance range analysis of the x-ray line profiles for seven cottons (native, ureatreated, and mercerized) has been carried out to get two estimates of the crystallite size from (1) the slope and (2) the variance intercept. Assuming the crystallite length of cellulose to be the same in ramie and native cottons under ideal conditions of growth, the relative fluctuation of the repeat length along the b-axis has been calculated for all the samples. This degree of paracrystalline lattice distortions is negatively correlated with the fiber bundle strength at zero gauge and appears to be the same as the imperfections referred to in the weak link theories of fiber strength. While the orientation parameters are also well correlated with strength, the degree of crystallinity does not seem to have any influence. Wilson's rigorous mathematical treatment of the number-average particle size, in relation to the two estimates from the variance slope and intercept as well as the particle size distribution, has been successfully applied for the first time to cotton fibers leading to a clearer understanding of crystallite size-strength relationship.
    Additional Material: 5 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 449-460 
    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 copolymer (MW = 1800) of styrene (St) and maleic anhydride (MAn) was esterified with an excess amount of an alcohol mixture, and then the relation between the esterification rates of the individual alcohols and the contents of the esters in the esterific copolymer was examined. At first, the rate constant of an individual esterification was obtained for four different alcohols (n-butanol, i-amylalcohol, and benzylalcohol) in a noncatalyst system. Then, the mixed esterification of n-butanol and i-amylalcohol was carried out; from the analysis of the ester contents, the following equation was obtained: $$ {{\left[ {{\rm P}_{\rm 1} } \right]} \mathord{\left/ {\vphantom {{\left[ {{\rm P}_{\rm 1} } \right]} {\left[ {{\rm P}_{\rm 2} } \right]}}} \right. \kern-\nulldelimiterspace} {\left[ {{\rm P}_{\rm 2} } \right]}} = {{k_1 \left[ {{\rm B}_{\rm 1} } \right]_0 } \mathord{\left/ {\vphantom {{k_1 \left[ {{\rm B}_{\rm 1} } \right]_0 } {k_2 \left[ {{\rm B}_{\rm 2} } \right]_0 .}}} \right. \kern-\nulldelimiterspace} {k_2 \left[ {{\rm B}_{\rm 2} } \right]_0 .}} $$ From this result, it was concluded that, in esterification with alcohols involving n species, the content of the individual ester can be expressed by the following equation: $$ {{\left[ {{\rm P}_j } \right]} \mathord{\left/ {\vphantom {{\left[ {{\rm P}_j } \right]} {\sum\limits_{i = 1}^n {\left[ {{\rm P}_i } \right]} }}} \right. \kern-\nulldelimiterspace} {\sum\limits_{i = 1}^n {\left[ {{\rm P}_i } \right]} }} = {{k_j \left[ {{\rm B}_j } \right]_0 } \mathord{\left/ {\vphantom {{k_j \left[ {{\rm B}_j } \right]_0 } {\sum\limits_{i = 1}^n {k_i \left[ {{\rm B}_i } \right]_0 } }}} \right. \kern-\nulldelimiterspace} {\sum\limits_{i = 1}^n {k_i \left[ {{\rm B}_i } \right]_0 } }} $$ where [P] = concentration of esters in the copolymer, [B]0 = initial concentration of alcohols, and k = rate constant of esterification (i,j = 1,2…,n).
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