2010
DOI: 10.1016/j.apcatb.2009.12.015
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On the kinetics and mechanisms of photolytic/TiO2-photocatalytic degradation of substituted pyridines in aqueous solutions

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Cited by 54 publications
(22 citation statements)
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“…2-HPY (P 1 ), is directly produced from 2-CPY and it is subsequently forming Dewar pyridinone (product P 2 ) as in the case of other 2-halogenated pyridines while a small amount of 2-CPY reacts directly to form Dewar pyridinone [2]. Products P 2 (5-azabicyclo[2.2.0]hex-2-en-6-one), P 3 (1H-pyrrole-2-carboxaldehyde), P 4 (6-hydroxy-2(1H)-pyridinone), P 5 (N-formyl-3-carbamoylpropenal) and P 11 (2-pyridinecarbonitrile) have been also identified in the degradation of other 2-halogenated pyridines [2], while products P 5 and P 9 (6-chloro-2-pyridinecarboxylic acid) were also found to form during 2-CPY photocatalysis [32]. Moreover, products P 5 and P 11 were also identified during 2-fluoropyridine photocatalysis [32].…”
Section: Photolytic Treatment Of 2-cpymentioning
confidence: 94%
“…2-HPY (P 1 ), is directly produced from 2-CPY and it is subsequently forming Dewar pyridinone (product P 2 ) as in the case of other 2-halogenated pyridines while a small amount of 2-CPY reacts directly to form Dewar pyridinone [2]. Products P 2 (5-azabicyclo[2.2.0]hex-2-en-6-one), P 3 (1H-pyrrole-2-carboxaldehyde), P 4 (6-hydroxy-2(1H)-pyridinone), P 5 (N-formyl-3-carbamoylpropenal) and P 11 (2-pyridinecarbonitrile) have been also identified in the degradation of other 2-halogenated pyridines [2], while products P 5 and P 9 (6-chloro-2-pyridinecarboxylic acid) were also found to form during 2-CPY photocatalysis [32]. Moreover, products P 5 and P 11 were also identified during 2-fluoropyridine photocatalysis [32].…”
Section: Photolytic Treatment Of 2-cpymentioning
confidence: 94%
“…Photocatalytic destruction of pollutants in aqueous solutions using NTO is facilitated mainly by a series of hydroxylation reactions initiated by hydroxyl radicals (· OH) [20][21][22][23][24][25][26]. Possible modes of · OH generation during NTO photocatalysis are shown in Figure 2.…”
Section: Mechanism and Kineticsmentioning
confidence: 99%
“…Pyridine and pyridine derivatives have received wide attention because of their occurrence in the environment and their hazardous effects on ecosystems and human health [4]. Picloram (4-amino-3,5,6-trichloro-2-pyridincarboxylic acid) is a potent herbicide that effectively controls the growth of broadleaf weed in pasture and rangeland, as well as in fields cultivated for wheat, barley, oats and woody plant species [5].…”
Section: Introductionmentioning
confidence: 99%