1965
DOI: 10.1021/ja01090a026
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Organic Polymers. Correlation between Their Structure and Catalytic Activity in Heterogeneous Systems. I. Pyrolyzed Polyacrylonitrile and Polycyanoacetylene

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Cited by 67 publications
(8 citation statements)
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“…In this manner, k AA directly predetermines the aging rate and indirectly (via the ratio k 0 AA /k age AA ) confines the scale of the effect. Thus, the coagulation efficiency during aging can be traced with the help of physical properties of the material, such as viscosity and surface tension, the higher surface tension the lower the coagulation efficiency (Manassen and Wallach 1965).…”
Section: Aging Kineticsmentioning
confidence: 99%
“…In this manner, k AA directly predetermines the aging rate and indirectly (via the ratio k 0 AA /k age AA ) confines the scale of the effect. Thus, the coagulation efficiency during aging can be traced with the help of physical properties of the material, such as viscosity and surface tension, the higher surface tension the lower the coagulation efficiency (Manassen and Wallach 1965).…”
Section: Aging Kineticsmentioning
confidence: 99%
“…Acetylene has been observed to decompose at 500°C to give compounds such as vinylacetylene and others (5,6,19]. The fiber may also undergo transformations at these temperatures, such as cyclization of nitrile groups, evolution of gases, and others E3, 5,14,20]. Such processes can disturb the order of the deposition or provide new reactant species.…”
Section: Resultsmentioning
confidence: 99%
“…4. Acetylene treatment-.interaction effects: The acetylene or decomposition products, or both, could react with or deposit on the fiber to produce new stronger compounds or coatings to heal over defects [2,5,6,17,19,20,26].…”
Section: Introductionmentioning
confidence: 99%
“…The reduced counterpart of quinone active sites is the hydroquinone formed by hydrogen atom abstraction from the organic substrate molecule. For ethylbenzene as the substrate, a transition state with the phenyl group in co-planar orientation with respect to the π-conjugated (a) trimerized phenanthrene quinone [42], (b) benzoquinone biphenyl copolymer [41], (c) polynaphthoquinone [40], (d) polyaniline [43], (e) pyrolyzed polyacrylonitrile [44]. Furthermore, the study of the ODH performance using 4-methyl-4-ethyl-1-cyclohexene as the substrate, which forms different reaction products depending on the acid/base properties of the catalyst, indicates that quinone-catalyzed ODH involves a homolytic C-H bond break rather than an ionic intermediate [40].…”
Section: Dehydrogenation Of Hydrocarbonsmentioning
confidence: 99%