1994
DOI: 10.1016/0008-6223(94)90045-0
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Nitrogen release in the gasification of carbons

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Cited by 47 publications
(25 citation statements)
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“…Carbonization of polyvinylcarbazole at 600 and 900°C is accompanied by the minimal release of nitrogen-bearing volatile products (HCN and NH 3 ) by comparison with the other two polymers, from which it is concluded that there is preferential conversion of five-membered nitrogen rings into quaternary nitrogen compounds, which subsequently participate in the form of a labile structure preceding graphitization. This agrees with conclusions on the pyrolysis of coals and carbonaceous plant products containing nitrogen in various cyclic modifications [41,42], which confirms the genetic relation between coal formation from natural and synthetic high-molecular compounds. In these papers, thermochemical transformations of carbonaceous materials under identical conditions, namely ones based on lignin and synthetic carbonizates obtained from carbazole, acridine, and polyacrylonitrile.…”
supporting
confidence: 89%
“…Carbonization of polyvinylcarbazole at 600 and 900°C is accompanied by the minimal release of nitrogen-bearing volatile products (HCN and NH 3 ) by comparison with the other two polymers, from which it is concluded that there is preferential conversion of five-membered nitrogen rings into quaternary nitrogen compounds, which subsequently participate in the form of a labile structure preceding graphitization. This agrees with conclusions on the pyrolysis of coals and carbonaceous plant products containing nitrogen in various cyclic modifications [41,42], which confirms the genetic relation between coal formation from natural and synthetic high-molecular compounds. In these papers, thermochemical transformations of carbonaceous materials under identical conditions, namely ones based on lignin and synthetic carbonizates obtained from carbazole, acridine, and polyacrylonitrile.…”
supporting
confidence: 89%
“…4d). These peaks were assigned to; (i) pyridinic-N at 397.9-398.6 eV, with the N atom contributing one electron to the p-system, (ii) pyrrolic-N at 399.1-399.8 eV with the N atom contributing two electrons to the psystem, (iii) graphitic-N (400.9-400.9 eV) with the N atom substituting the C atom in the graphitic structure 37,71 and (iv) NO X due to oxygenation of pyridinic-N (>402 eV). 70,72,73 The NCSs-H 2 comprised of 48% pyridinic-N, 21% pyrrolic-N and 22% graphitic-N and 9% NO X .…”
Section: Xps Analysis Of the N-doped Cssmentioning
confidence: 99%
“…After Cagniant et al [21], ammoxidation of cellulosic material leads to fixation of 60% of nitrogen as imine which gives pyridinic nuclei, while the synthesis of pyrrolic nucleus occurs also by reaction of ammonia with dicarbonyl moieties. After Thomas et al [30,31], formation of pyrrolic, pyridinic and pyridine N-oxide functions at the edge and in the interior of the poly-aromatic systems (graphene layers) would depend on the isotropic/anisotropic character of the carbon and on the fact that the ammonia treatment is performed during or after carbonization.…”
Section: 2 Surface Groups Characterization After Modification With mentioning
confidence: 99%