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  • Polymer and Materials Science  (14,995)
  • Inorganic Chemistry  (1,777)
  • Numerical Methods and Modeling  (1,287)
  • Geophysics  (1,232)
  • 1995-1999  (19,291)
Collection
Keywords
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 51 (1995), S. 703-709 
    ISSN: 1420-9071
    Keywords: Geophysics ; geology ; natural radioactivity ; radiometry ; mining ; uranium ores ; radon ; disposal of radioactive waste
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Almost simultaneously with Roentgen rays, natural radioactivity was discovered. Its investigation led to important fundamentals of the geosciences: petrophysics, terrestrial heat flow, isotope geology, and absolute geological chronology. In applied geophysics and geology, exploration of radioactive ores and of tectonic faults, and radiometric well loggings, are used. Production of radioactive water and mining for uranium ores are discussed, including their development (especially in the Saxon ore mountains) and the consequences on health (radon in underground air and houses). Disposal of radioactive waste is touched on briefly.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Astrophysics and space science 230 (1995), S. 439-456 
    ISSN: 1572-946X
    Keywords: Geophysics ; geomagnetic field
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Geomagnetic field research carried out at the Hermanus Magnetic Observatory over the past decade is reviewed. An important aspect of this research has been the study of geomagnetic field variations, with particular emphasis on ULF geomagnetic pulsations. Features of geomagnetic pulsations which are unique to low latitude locations have been investigated, such as the cavity mode nature of low latitude Pi 2 pulsations and the role played by ionosphericO + ions in the field line resonances responsible for Pc 3 pulsations. A theoretical model has been developed which is able to account for the observed relationships between geomagnetic pulsations and oscillations in the frequency of HF radio waves traversing ionospheric paths. Other facets of the research have been geomagnetic field modelling, aimed at improving the accuracy and resolution of regional geomagnetic field models, and the development of improved geomagnetic activity indices.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 7-13 
    ISSN: 0887-624X
    Keywords: radical terpolymerization ; charge transfer complexes ; phenanthrene ; maleic anhydride ; trans-stilbene ; thermal stability ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical terpolymerization of the donor-acceptor-donor monomer system, phenanthrene (P) - maleic anhydride (M) - trans-stilbene (S), was studied. These monomers are known to be nonhomopolymerizable. The terpolymerization was carried out in p-dioxane and/or toluene at 70°C in the presence of benzoyl peroxide used as the initiator. P and S were found to form charge transfer complexes (CTC) with M in p-dioxane at 35°C. The results obtained are discussed in terms of the free monomer and complex propagation models. It is shown that terpolymerization is carried out at a stage close to binary copolymerization of two complexomers. The reactivity ratio of P … M and S … M complexes was estimated by the Kelen-Tüdös method. Absorbance ratios at 1770 cm-1 (vC=0 of anhydride group), 764 cm-1 (δCH in monosubstituted benzene of S), and 820 cm-1 (δCH in disubstituted benzene of P) as a function of terpolymer composition were established. P - M - S terpolymers are shown to have high thermal stabilities. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1375-1380 
    ISSN: 0887-624X
    Keywords: poly(vinyl chloride) ; electrical conductivity ; photodehydrochlorination ; laminated films ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(vinyl chloride) (PVC) has been converted to an electrically conductive structure by combined electrochemical and photochemical methods. PVC was cast on a polypyrrole (PPy) film electrode which had been electrochemically prepared. The PVC layer in the laminated PVC/PPy films was first dehydrochlorinated under the illumination of UV light, and the generated polyenes were subsequently doped with I2 and FeCl3. The maximum electrical conductivity achieved for such PVC film was 2.51 X 10-2 and 8.63 10-2 S cm-1 after I2 and FeCl3 doping, respectively. The temperature dependence of the electrical conductivity showed different behavior in higher and lower temperature ranges. In the former (T 〉 243 K), the T-1 law held, and the activation energy and bandgap were estimated as 0.25 and 0.49 eV, respectively. In the latter (T 〈 243 K), the conductivity mechanism followed the variable range hopping model (T-1/4 law) in which the radius of the localized state wave function and the density of the localized states at the Fermi level were 1.25 × 103 Å and 1.03 X 1015 eV-1 cm-3, respectively. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1409-1417 
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; oligomers ; polystyrene ; hydrotalcite ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dominant species in the early stages of an emulsifier-free emulsion polymerization of styrene has been found to be an oligomer of two to three monomer units using a novel trapping technique. This involved the intercalation of charged primary oligomers between the layers of a hydrotalcite, [Mg4Al2(OH)12]2+[A]2- (where A = dianion). Hydrotalcites are an important class of lamellar, inorganic compounds whose interlayer spacing can be mod-ified by anion exchange. Our approach first involved preparing a hydrotalcite precursor in which the layers were propped apart by an organic dianion (terephthalate = TA). This material was then used to capture the negatively charged polystyrene oligomers from the emulsion polymerization reaction mixture. We found that TA was rapidly ion-exchanged for the charged oligomers.The resulting pillared hydrotalcite material was characterized using XRD and SEC. We found that the interlayer spacing between the hydroxide layers increased to 23.2 Å on exposure to the emulsion reaction mixture. This represents an interlayer expansion of 18.3 Å (after subtraction of the hydroxide layer contribution), which is cnsistent with intercalation of oligomers with two to three monomer units arranged in a bilayer. This size estimate was confirmed by the results of size exclusion chromatography. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1455-1460 
    ISSN: 0887-624X
    Keywords: γ-oxidation ; polyethylene ; FTIR ; molecular weight ; elongation at break ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: γ-Oxidation of linear low-density polyethylene based on hexene and butene was investigated. Irradiation was performed at different dose rates in air (from 2 rad/s to 100 rad/s). Degraded samples were analyzed with IR combined with NO and SF4 derivatizations. Our results showed that the lower the dose rate, the higher the degree of oxidation in terms of γ-product formation. Ketone species appeared to be the dominant γ-products. The G values of γ-product formation were very dependent on the dose rate of initiation. Comparison of the G value ratio of different γ-products revealed stoechiometry differences. The complex appearance and disappearance of unsaturations was tentatively explained. The modifications of elongation at break induced by γ-irradiation were monitored by molecular changes in weight. This was not conclusive because changes in elongation at break are inconsistent with changes in Mw/Mn. © 1995 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1465-1474 
    ISSN: 0887-624X
    Keywords: grafting ; poly(styrene-graft-ethylene oxide) ; styrene-oxirane graft copolymers ; ethoxylation ; alkylation ; anionic polymerization of ethylene oxide ; poly(styrene-co-acryl-amide) ; crystallinity ; water absorption ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(styrene-graft-ethylene oxide), having alkyl chains (C12 or C18) on the polystyrene main chain or on the poly(ethylene oxide) (PEO) side chains, were synthesized. The main chain was alkylated by first ionizing amide groups in a styrene/acrylamide copolymer with tert-butoxide, and then using the amide anions as sites for reactions with 1-bromoalkanes. An excess of amide anions was used in the reaction, and the remaining anions were subsequently utilized as initiator sites for the anionic polymerization of ethylene oxide (EO). Synthesis of poly(styrene-graft-ethylene oxide) with alkylated side chains was accomplished by polymerization of EO onto the ionized styrene/acrylamide copolymer, followed by an alkylation of the terminal alkoxide anions with 1-bromoalkanes. The alkylated graft copolymers were structurally characterized by using elemental analysis, 1H NMR, GPC, and IR spectroscopy. DSC analysis showed that only graft copolymers with PEO contents exceeding about 50 wt % and side chain crystallinities comparable to those of homo-PEO. Main chain alkylated graft copolymers generally had higher crystalinities, as compared to nonalkylated and side chain alkylated samples. The graft copolymers absorbed water corresponding to one water molecule per EO unit at low PEO contents. The water absorption increased progressively at PEO contents above 30 wt % for main chain alkylated samples and above 50 wt % for non-alkylated samples. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1419-1429 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No Abstract
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1447-1454 
    ISSN: 0887-624X
    Keywords: terpolymerization ; charge transfer complex ; allylglycidyl ether ; maleic anhydride ; methyl methacrylate ; thermo-crosslinking ; photo-crosslinking ; thermal degradation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical copolymerization of donor-acceptor monomers, i.e., allylglycidyl ether (AGE), maleic anhydride (MA) and methyl methacrylate (MMA) are studied, where binary copolymerization of AGE...MA complex with MMA is obtained. Constants of charge transfer complex formation (Kc) and copolymerization (r1 and r2) are determined by 1H-NMR and Kelen-Tüdöş methods, respectively. It is found that synthesized film-forming terpolymers with free epoxy and anhydride groups on side chain of macro-molecules are being crosslinked easily under the effect of temperature and/or UV-ir-radiation. Observed crosslinking effect is proved by the DTA, TGA, and IR spectroscopic analyses. It is shown that complex-radical terpolymerization is very convenient method for the designing of reactive functional macromolecules of linear structure with self-crosslinking properties which can serve as a basis for the use in photolithographic applications. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 10
    ISSN: 0887-624X
    Keywords: saccharic acid ; dilactone ; polyaddition ; polyurethane ; diisocyanate ; deg-radation ; hydrolysis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyaddition of saccharic acid dilactones prepared from D-glucose and D-mannitol, D-glu-caro-, and D-mannaro-1,4:6,3-dilactones (1 and 2, respectively), with hexamethylene di-isocyanate (3a) and methyl (S)-2,6-diisocyanatocaproate (3b) was carried out by using dibutyltin dilaurate as a catalyst at 50, 25, and 0°C to give polyurethanes (4 and 5) having dilactone moieties in the main chains. The resulting polymers were found to decompose easily in phosphate buffers under neutral or slightly basic conditions (pH 7 or 8). Therefore, the polyurethanes may be used as novel degradable polymeric materials. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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