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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    International journal of thermophysics 7 (1986), S. 1091-1100 
    ISSN: 1572-9567
    Schlagwort(e): electrical conductivity ; La2CuO4 ; La2NiO4 ; Nd2CuO4 ; oxides ; phonons ; thermal conductivity ; thermal expansion
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Thermal conductivity of polycrystalline La2CuO4, La2NiO4, and Nd2CuO4 was measured in the temperature range 300–1000 K. No anomaly in thermal conductivity has been observed during the semiconductor-to-metal transition of La2NiO4 or in the metallic phases of La2CuO4 and La2NiO4. A change of slope has been found, however, in the thermal conductivity of La2CuO4 at the crystallographic transition. The thermal conductivity of the oxides is mainly phononic in this temperature range.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Catalysis letters 19 (1993), S. 281-291 
    ISSN: 1572-879X
    Schlagwort(e): Benzyl alcohol reactions on zeolites ; anthracene, from benzyl alcohol ; stilbene, from benzyl alcohol ; benzyl alcohol, formation of anthracene from ; stilbene, formation of anthracene from ; zeolites, reaction of benzyl alcohol over
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The reaction of benzyl alcohol and dibenzyl ether on several zeolites was studied in the temperature range 300–500 °C. The major products were benzaldehyde and toluene due to disproportionation, anthracene due to intermolecular alkylation followed by cyclodehydration, benzyltoluenes due to alkylation followed by hydrogenolysis, and stilbene. The alkylation course was strongly influenced by shape selectivity with the large pore zeolites mainly yielding anthracene and the medium pore zeolites benzyltoluene. The formation of stilbene was a new observation which has a bearing on the mechanism of the methanol-to-hydrocarbon reactions.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 1069-1073 
    ISSN: 0887-624X
    Schlagwort(e): cardanol ; cardanyl acrylate ; self-crosslinkable polymer ; autooxidation ; hydroperoxide ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Cardanyl acrylate (CA), a monomer that yields crosslinkable copolymers, was synthesized by the reaction of cardanol with acryloyl chloride. A linear polymer was obtained by solution polymerization of the monomer in toluene using 0.8% azobisisobutyronitrile as initiator. Upon removal of solvent, the polymer undergoes crosslinking on exposure to air (or UV light) to give an insoluble transparent film. However, in bulk and suspension polymerization the polymer undergoes in situ crosslinking in the absence of any crosslinking agent. The polymer was characterized by IR, NMR, DSC, and GPC. The crosslinking reaction of soluble polymer on exposure to air at ambient conditions was explained by the hydroperoxide theory. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2851-2856 
    ISSN: 0887-624X
    Schlagwort(e): poly(1,3-phenyl ocatnoate) ; synthesis ; characterization ; thermal decomposition ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Poly(1,3-phenyl octanoate) (polyHPOA) was prepared by melt and solution polycondensation methods from 8-(3-hydroxyphenyl)octanoic acid (HPOA), a novel monomer useful as a chain disruptor in liquid crystalline copolyesters. The melt polycondensation technique gave a polyester of higher inherent viscosity (0.80 dL/g in p-chlorophenol) than that (0.75 and 0.56 dL/g, respectively, for the Ogata method and thionyl chloride/pyridine method in the same solvent) of solution techniques. The solubility of the polyesters was limited to strongly acidic and polar solvents. The polyester was characterized by elemental analysis, IR spectroscopy, WAXD, TGA, isothermal TGA and DTA. x-ray diffraction pattern of the polyesters indicated that it is amorphous in nature. TGA of the polyesters gave a thermal stability of 470°C in nitrogen atmosphere at 50% decomposition. The available thermal data suggest that the polyester undergoes thermal decomposition by a pyrolytic cleavage involving the ester linkage with the formation of ketene and phenol ended groups as intermediates. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 309-315 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The kinetics and mechanism of oligomerization of cardanol over acid catalysts were studied. GPC results showed the formation of a mixture of oligomers such as dimer, trimer, tetramer, etc. IR spectra of the products of oligomerization showed a decrease in the intensity of the double bond absorption band at 1630 cm-1 and the disappearance of terminal vinyl bands at 895 cm-1 and 907 cm-1. 1H NMR spectra showed drastic changes in the unsaturated proton resonance signals at 5.5δ with respect to saturated protons at 0.2-2.5δ. The ratio of resonance integrals of unsaturated to saturated protons decreased from 1 : 6.5 to 1 : 20 after oligomerization. GPC studies showed that the rate of formation of the dimer, trimer, tetramer, etc. follow an identical path and that the individual oligomers are formed in the same weight percentage at any time during the reaction. A kinetic scheme is proposed to explain this phenomenon. Kinetic studies showed that the oligomerization reaction follows first order kinetics with respect to the monomer concentration and the rate constant is K = 6.6 × 10-5s-1. A probable mechanism for the oligomerization of cardanol is proposed.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 53 (1994), S. 1415-1423 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Cardanyl acrylate/methacrylate on suspension polymerization with methyl methacrylate, styrene, and acrylonitrile yielded copolymer beads. The beads were almost uniform in size and cross-linked in nature. The copolymers synthesized were characterized by infrared, thermogravimetric analysis, scanning electron and optical microscopy, and swelling studies. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 1765-1775 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The cationic polymerization of cardanol using borontrifluoridediethyletherate as initiator has been investigated by gel permeation chromatographic techniques. The molecular weight and molecular weight distribution of the polymer at different temperatures and various initiator concentrations were studied, and the polymerization conditions have been optimized as 140°C with an initiator concentration of 1%. The reaction was found to follow first-order kinetics with respect to the monomer. The activation energy and rate constants for the system have also been evaluated. The polymer has been characterized by IR, 1H and 13C-NMR spectra.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 981-987 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Processability characteristics of ethylene-vinyl acetate (EVA) copolymer formulations modified with a flame-retardant 3-(tetrabromopentadecyl) 2,4,6-tribromo phenol (TBPTP) have been studied on a Brabender Plasticorder at various shear rates and temperatures. The plasticizing effect of TBPTP on EVA has been confirmed by the increase in flow behavior index and decreases in melt viscosity, melt elasticity, and activation energy of melt flow. The improvement in processability of the TBPTP-modified EVA over the unmodified sample was reflected in a reduction in power consumption during mixing of the former. The study was undertaken because of the potential of TBPTP-modified EVA for application in flame retardant low smoke (FRLS) cable sheathings. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 2129-2135 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Cardanol was functionalised to incorporate elements such as phosphorus and bromine and polymerised with formaldehyde or hexamethylenetetramine (HMTA) to get flame retardant polymers. Thus, monocardanyl phosphoric acid (MCPA), its bromoderivative (BrMCPA), and their formaldehyde condensates (MCPAF and BrMCPAF) and cross-linked polymers were prepared and characterized by IR, NMR, and GPC. Flammability and thermal stability of these polymers were evaluated by LOI and TGA, respectively, and compared with those of conventional cardanol-formaldehyde (CF) resin and its bromoderivative. TGA of MCPAF showed that although it is initially less stable than that of CF, its stability increases above 500°C over that of CF. Char yields of MCPAF and BrMCPAF are 21 and 27, respectively, and corresponding LOI values are 27 and 49. The present data do not support any synergism nor any additive effect between phosphorus and bromine, but a positive interaction between them is indicated with phosphorus mainly contributing in the condensed phase and bromine in the vapour phase mechanism. The activation energies in the range 20-30 kcal/mol for MCPAF suggest an ionic mechanism for its decomposition, whereas mainly a free radical type of decomposition is inferred for BrMCPAF with an activation energy in the range of 35-50 kcal/mol. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 429-438 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Phenolic resins with improved/altered thermal stability and flame retardancy were prepared by introducing flame retardant elements such as phosphorus and bromine at the monomer stage, followed by condensation with formaldehyde or hexamethylene tetramine (HMTA). Thus, monophenyl phosphoric acid (MPPA), monophenyl phosphoric acid-formaldehyde resin (MPPAF), brominated phenol-formaldehyde resin (BrPF) and 2,4,6-tribromophenyl-phosphoric acid-formaldehyde resin (BrMPPAF) were prepared and characterised. Thermal stability and flammability of these polymers were evaluated by TGA and LOI respectively and compared with those of phenol-formaldehyde resin (PF) and phosphorylated phenol-formaldehyde resin (PPF). The TGA (in air) of MPPAF showed enhanced thermal stability (char yield 66%) over that of PF (char yield 52%) and PPF (char yield 58%) indicating the role of phosphorus in imparting thermo-oxidative resistance to PF. The enhancement is better when phosphorus is introduced at the monomer stage. The incorporation of bromine, however, brought about an unexpected reduction in the thermal stability of PF (char yield: BrPF, 2% and BrMPPAF, 26%). Both phosphorus and bromine are found to enhance the LOI values of PF (cured) from 35 to 50, 48, and 56, respectively, for MPPAF, BrPF, and BrMPAFF. A comparison of LOI values of these resins with their char yield suggests a condensed phase mechanism for phosphorus and vapor phase mechanism for bromine operating during thermal decomposition. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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