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  • 1
    Electronic Resource
    Electronic Resource
    Photopolymerization of methyl methacrylate using a combination of rhodamine 6G and benzoyl peroxide as photoinitiator in nonaqueous media (1986)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 1053-1063 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photopolymerization of methyl methacrylate (MMA) in visible light was studied at 40°C using Rhodamine 6G - Benzoyl peroxide combination as photoinitiator. The photopolymerization proceeds by a free radical mechanism and the radical generation process occurs by an initial complexation reaction between the initiator components. Kinetic data indicated a lower-order dependence of Rp on initiator concentrations (initiator exponent 〈 0.5). Initiator-dependent chain termination was significant along with the bimolecular mode of chain termination.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1986.080240520
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  • 2
    Electronic Resource
    Electronic Resource
    Effect of pressure on the free radical solution polymerization of acrylonitrile and methylmethacrylate (1987)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 25 (1987), S. 187-191 
    Details
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1987.140250407
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  • 3
    Electronic Resource
    Electronic Resource
    N-Vinylcarbazole polymerization by 3d-transition metal ion exchanged 13x molecular sieve: Dual initiation mechanism (1986)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 24 (1986), S. 363-369 
    Details
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1986.140240801
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  • 4
    Electronic Resource
    Electronic Resource
    Synthesis and evaluation of a polyimide containing carbazole and naphthalene moiety (1990)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3795-3800 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1990.080281322
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  • 5
    Electronic Resource
    Electronic Resource
    Chemiluminescenz bei der Oxydation von fluorescierenden und nicht fluorescierenden Stoffen durch Wasserstoffperoxyd und Ozon (1929)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 186 (1929), S. 154-158 
    Details
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1. Wenn zahlreiche fluorescierende oder nicht fluorescierende Farbstofflösungen durch Wasserstoffperoxyd in Gegenwart von Ferrosulfat oxydiert werden, tritt ein Glimmen auf, das im dunklen Raume zu erkennen ist.2. Die Wellenlangen der Glimmerscheinung bei der Oxydation einiger fluorescierender Fnrbstoffe durch ozonisierten Sauerstoff sind gemessen worden.3. Kieselsaure mit etwas adsorbiertem Neutralrot zeigt in einer Suspension in Äthylallrohol bei Behandlung mit ozonisiertem Sauerstoff eine Glimmerscheinung.4. Wenn kleine Mengen eines Farbstoffes, der gutes Glimmen zeigt , rnit einem anderen Farbstoff von schwachem Glimmvermogen gemischt werden, so liefert das Gemisch bei Behandlung mit Ozon ein starkeres Glimmen als der schwächer glimmende Farbstoff allein.5. Steigerung der Temperatur führt zur Verstarkung des Glimmens bei der Oxydation von Reduktionsmitteln durch Ozon oder Wasserstoffperoxyd.6. Zunahme der Konzentration der Reduktionsmittel verursacht eine Steigerung der Glimmintensitat bis zu einem Grenewert. Wird die Konzentration weiter gesteigert, so schwacht sich das Glimmen ab und hört schließlich auf.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19291860111
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  • 6
    Electronic Resource
    Electronic Resource
    SAXS investigations on chiral liquid crystalline polymers: antiferroelectric and ferrielectric structures? (1992)
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 3 (1992), S. 257-262 
    Details
    ISSN: 1042-7147
    Keywords: Chiral liquid crystalline polymers ; Antiferroelectricity ; Ferrielectricity ; SAXS ; 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
    Notes: The structure and phase behavior of liquid crystalline polymers (LCPs) having a common chiral side chain mesogen but different main chain structures have been investigated using small-angle X-ray scattering (SAXS). While the low molecular weight chiral side chain mesogen by itself exhibits ferroelectricity, the SAXS data of the side chain LCP with a flexible polyacrylate backbone contains a bilayered superstructure peak that is indicative of antiferroelectric order. The combined LCP with a nonpolar main chain mesogen also has a bilayered superstructure, but has a different structural organization in the proposed antiferroelectric phase compared to the side chain LCP. Further changes in the phase behavior and structural organization occur when a polar group is introduced into the main chain mesogen. A ferrielectric phase has been proposed to explain the observation of a trilayered superstructure in the corresponding SAXS data. The influence of the chemical structure and connectivity on the phase behavior and superstructure formation in the chiral LCPs is discussed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pat.1992.220030510
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  • 7
    Electronic Resource
    Electronic Resource
    Synthesis and some properties of anthracene and anthraquinone incorporated poly(vinyl chloride) and the ion exchange resin therefrom (1989)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 38 (1989), S. 1641-1651 
    Details
    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) has been modified by chlorine displacement reaction with 2-anthrol and anthraquinone-2-ol. The condensates (PVC-ACOL and PVC-AQOL) are insoluble in all solvents common to PVC and have been characterized by elemental and IR spectra analysis. The initial decomposition temperature of these condensates follow the trend: PVC-AQOL (250°C) 〉 PVC-ACOL (200°C) 〉 PVC(190°C) and the overall thermal stabilities beyond 60% decomposition follows the same trend. Permittivity and dielectric loss of these condensates sharply fall with increasing applied frequency (10-1.3 ×107 Hz) to a limiting constant value. In contrast, for unmodified PVC these values are low and remain independent of frequency in the same range. Sulfonation of these PVC condensates affords a weak acid resin with —COOH and —OH ionogenic groups, but no strong sulfonic acid groups due presumably to oxidative degradation of the PVC matrix.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1989.070380905
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  • 8
    Electronic Resource
    Electronic Resource
    Synthesis and thermal stability, dielectric, and conductivity characteristics of polymers with pendant and backbone anthracene sulfonyl groups (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 2489-2498 
    Details
    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: Anthracene-mono- and disulfonyl derivatives of polystyrene and poly (N-vinylcarbazole) have been prepared and the thermal stability, dielectric, and conductivity of these polymer pendant sulfones have been evaluated. The anthracene-based benzene, naphthalene, anthracene, and biphenyl copolysulfones have also been prepared and characterized in regard to the above-cited properties. Interesting variations in these properties between these two classes of polymers carrying pendant and backbone sulfonyl groups have been noted and rationalised from structural considerations.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1991.070420914
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  • 9
    Electronic Resource
    Electronic Resource
    Polymer blend: A novel method for the preparation of a natural rubber-carboxylated nitrile rubber blend (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 1007-1014 
    Details
    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: Bis(diisopropyl)thiophosphoryl disfulfide (DIPDIS) can be successfully used to form a blend comprising polar carboxylated nitrile rubber (XNBR) and nonpolar NR through a chemical link between the two. It is revealed from the study that the physical properties of the vulcanizates obtained from the NR-XNBR blend could be significantly improved by the judicious selection of the NR:XNBR ratio. These properties can further be improved by two-stage vulcanization as described in the procedure. The SEM study reveals that it is possible to form a coherent blend of NR and XNBR in the presence of DIPDIS. © 1994 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1994.070520801
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  • 10
    Electronic Resource
    Electronic Resource
    Thiophosphoryl disulfides: Novel coupling agents for styrene-butadiene rubber/carboxylated nitrile rubber blends (1995)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 981-993 
    Details
    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: Thiophosphoryl disulfide was successfully used as a novel coupling agent to form a coherent blend comprising polar carboxylated nitrile rubber (XNBR) and nonpolar styrene-butadiene rubber (SBR) establishing close proximity between them through chemical bridging. The study reveals that XNBR in the presence of thiophosphoryl disulfide greatly improves the physical properties of SBR and thus acts as a reinforcing filler. It is noted that the physical properties of the vulcanizates obtained from the SBR-XNBR blend depend upon the SBR : XNBR ratio and the mode of cure. SEM studies corroborate the observed facts. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1995.070580604
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