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  • Physics  (8)
  • LUNAR AND PLANETARY EXPLORATION  (4)
  • 1980-1984  (11)
  • 1965-1969  (1)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1155-1166 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyesters containing conjugated diacetylenic groups in the polymer backbone were synthesized by interfacial condensation of 3,5-hexadiyne-1,6-diol and diacid chlorides of succinic, glutaric, adipic, azealic, sebacic, terephthalic, and isophthalic acids. The polyesters were characterized by their infrared and ultraviolet absorption spectra, elemental analysis, and viscosity measurements. Powder x-ray patterns indicated high degress of crystallinity. The polyesters were found to be highly photoreactive. The relative photoreactivities of the polyester films were determined by the adhesion method. Only small differences in the reactivity have been observed despite structural changes in the R group in the polymer backbone. Differential thermal analysis behavior of all polymers in the temperature range ambient to 300°C and isothermal behavior of HGI at two different temperatures have been studied.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3081-3092 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the presence of ZnEt2 the CoCl2-quinoline complex polymerizes NVC with a rate increasing with ZnEt2 and CoCl2-Q concentrations up to a certain concentration of ZnEt2 or CoCl2-Q, thereafter becoming independent of either. At a fixed concentration of ZnEt2 and CoCl2-Q the rate is second order with respect to NVC. The poly(NVC) obtained is freely soluble in benzene but leaves some insoluble fraction in methyl ethyl ketone, which has been characterized by 13C-NMR to be a stereoblock polymer. X-ray diffraction, IR, and thermal characteristics of the polymer have also been reported. [η] is virtually independent of monomer, in the concentration range 0.1-0.25 mol/L ZnEt2 and CoCl2-Q concentrations. Oxygen as an additive inhibits the polymerization. A cationic coordination mechanism has been proposed and appropriate rate and degree of polymerization equations have been suggested.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1861-1866 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3155-3164 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new polymeric azodye has been synthesized from carbazole by diazotization of its derivative N-methylcarbazole-3,6-diamine and subsequent coupling reaction with 2,2-bis(4-hydroxyphenyl-3-sulfonate-Na)-propane prepared from bisphenol-A. Its physico-chemical, electrical, and thermal properties have been characterized; finally, its application to the preparation of colored semiconductive films from polyvinyl alcohol has been studied.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 3347-3352 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2017-2026 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A low temperature solution condensation method with pyridine as acceptor-catalytic reagent was applied to the synthesis of polyarylates from carbazole and bisphenol A/phenolphthalein. The polyarylates were classified with respect to their structure, thermal stability, and dielectric behavior.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1997-2004 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copper(II)-exchanged-13X molecular sieves, prepared from four copper(II) salts, namely, sulfate, nitrate, chloride, and acetate, and their activities in the polymerization of N-vinylcarbazole at a fixed copper ion exchange level were studied. From the kinetic characteristics of polymerization it was established that the variation in activities of the Cu-exchanged sieves is due primarily to the difference in the pH of the original salt solution, which is responsible for the varying degree of proton exchange with the zeolite during copper ion exchange. A first-order dependence of the rate of polymerization was observed with respect to H+ ion concentration of the original copper-salt solution. It was further established that the rate of polymerization of exchanged copper ion, at a hypothetical zero proton concentration, is low. A mechanism of polymerization of NVC on copper-exchanged-13X zeolite was suggested on the basis of the results obtained.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 135-149 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A few redox systems containing thiourea as reductant have been found to be quite effective in initiating vinyl polymerization in aqueous media and polymers obtained in the process have all been found to contain amino endgroups to various extents by the application of dye techniques. Quite a few oxidants have so far been utilized for this purpose; among them are ferric chloride (Fe3+), ethylene dibiguanide complex salts of tripositive silver (Ag3+), hydrogen peroxide (H2O2), persulfate (S2O82-), bromate (BrO3-) + hydrochloric acid (HCl). In case of oxidants Fe3+ and Ag3+, amino endgroups are mainly incorporated in polymers; but in case of oxidants H2O2 and S2O82-, fragments of oxidants are also incorporated as hydroxyl and sulfate endgroups. BrO3-, however, forms a very efficient redox-initiating system with thiourea, as is evidenced by its capability of polymerizing even hydroquinone-stabilized water-soluble vinyl monomers at very low temperature (∼0°C.) and at a quite rapid rate. Besides amino endgroups, sulfonate endgroups have also been detected in polymers in this case, and the relative extents of these two types of endgroups depend generally on the acid concentration of the system. Evidences so far collected indicate the generation of S—C(=NH)NH2 radicals in the system by oxidation of isothiourea, HS—C(=NH)NH2, and these are incorporated in polymers as endgroups. Sulfonate endgroups may be generated by oxidation of these amino-bearing endgroups. Suitable initiation mechanisms have been suggested in each case.
    Additional Material: 5 Tab.
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  • 9
    Publication Date: 2019-06-28
    Description: Petrologic data and contents of Ag, Bi, Cd, Co, Cs, Ga, In, Rb, Se, Te, Tl and Zn-trace elements spanning the volatility/mobility range-in light and dark portions of H chondrite regolith breccias and L chondrite fragmental breccias are reported. The chemical/petrologic characteristics of H chondrite regolith breccias differ from those of nonbrecciated chondrites or fragmental breccias. Petrologic characteristics and at least some trace element contents of H chondrite regolith breccias reflect primary processes; contents of the most volatile/mobile elements may reflect either primary or secondary processing, possibly within layered H chondrite parent object(s). Chemical/petrologic differences existed in different regions of the parent(s). Regoligh formation and gardening and meteoroid compaction were not so severe as to alter compositions markedly.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Geochimica et Cosmochimica Acta; 47; Feb. 198
    Format: text
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  • 10
    Publication Date: 2019-06-28
    Description: The neutron activation data for Ag, As, Bi, Cd, Co, Cs, Cu, Ga, In, Rb, Se, Te, Tl, and Zn were obtained in samples of Abee heated to 1000-1400 C at low pressures. In addition, these elements were reported in nine enstatite achondrites and in the silicate part of the Mt. Egerton stony-iron. The data show trace element losses above 1000 C by diffusion-controlled processes with apparent activation energies of 8 to 55 kcal/mol; these data together with abundances of aubrites, Mt. Egerton, and E4-6 chondrites, and isotopic results link all enstatite meteorites to a common parent body. The data also indicate that aubrites and the Mt. Egerton material reflect fractional crystallization of a magma produced from enstatite chondrite-like parent material (E6) and the late introduction of chalcophiles and mobile elements transported by an FeS-Fe eutectic from an E4-6 region undergoing open-system metamorphism.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Geochimica et Cosmochimica Acta; 44; Dec. 198
    Format: text
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