Effect of Calcination Time on the Physicochemical Properties and Photocatalytic Performance of Carbon and Nitrogen Co-Doped TiO2 Nanoparticles; Catalysts; Vol. 10, iss. 8

Bibliographic Details
Parent link:Catalysts
Vol. 10, iss. 8.— 2020.— [847, 27 p.]
Corporate Author: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий Научно-исследовательский центр "Физическое материаловедение и композитные материалы"
Other Authors: Massima M. E. S. Mouele Emile Salomon, Dinu M. Mihaela, Cummings F. Franscious, Fatoba O. O. Ojo, Zar Myint M. T. Myo Tay, Kyaw H. H. Htet Htet, Parau A. C. Anca Constantina, Vladesku A. Alina
Summary:Title screen
The application of highly active nano catalysts in advanced oxidation processes (AOPs) improves the production of non-selective hydroxyl radicals and co-oxidants for complete remediation of polluted water. This study focused on the synthesis and characterisation of a highly active visible light C–N-co-doped TiO2 nano catalyst that we prepared via the sol-gel method and pyrolysed at 350 °C for 105 min in an inert atmosphere to prevent combustion of carbon moieties. Then we prolonged the pyrolysis holding time to 120 and 135 min and studied the effect of these changes on the crystal structure, particle size and morphology, electronic properties and photocatalytic performance. The physico-chemical characterisation proved that alteration of pyrolysis holding time allows control of the amount of carbon in the TiO2 catalyst causing variations in the band gap, particle size and morphology and induced changes in electronic properties. The C–N–TiO2 nano composites were active under both visible and UV light. Their improved activity was ascribed to a low electron–hole pair recombination rate that enhanced the generation of OH· and related oxidants for total deactivation of O.II dye. This study shows that subtle differences in catalyst preparation conditions affect its physico-chemical properties and catalytic efficiency under solar and UV light.
Language:English
Published: 2020
Subjects:
Online Access:https://doi.org/10.3390/catal10080847
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=664427

MARC

LEADER 00000naa0a2200000 4500
001 664427
005 20250814120322.0
035 |a (RuTPU)RU\TPU\network\35611 
035 |a RU\TPU\network\35599 
090 |a 664427 
100 |a 20210413d2020 k||y0engy50 ba 
101 0 |a eng 
135 |a drcn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Effect of Calcination Time on the Physicochemical Properties and Photocatalytic Performance of Carbon and Nitrogen Co-Doped TiO2 Nanoparticles  |f M. E. S. Massima, M. Dinu, F. Cummings [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 74 tit.] 
330 |a The application of highly active nano catalysts in advanced oxidation processes (AOPs) improves the production of non-selective hydroxyl radicals and co-oxidants for complete remediation of polluted water. This study focused on the synthesis and characterisation of a highly active visible light C–N-co-doped TiO2 nano catalyst that we prepared via the sol-gel method and pyrolysed at 350 °C for 105 min in an inert atmosphere to prevent combustion of carbon moieties. Then we prolonged the pyrolysis holding time to 120 and 135 min and studied the effect of these changes on the crystal structure, particle size and morphology, electronic properties and photocatalytic performance. The physico-chemical characterisation proved that alteration of pyrolysis holding time allows control of the amount of carbon in the TiO2 catalyst causing variations in the band gap, particle size and morphology and induced changes in electronic properties. The C–N–TiO2 nano composites were active under both visible and UV light. Their improved activity was ascribed to a low electron–hole pair recombination rate that enhanced the generation of OH· and related oxidants for total deactivation of O.II dye. This study shows that subtle differences in catalyst preparation conditions affect its physico-chemical properties and catalytic efficiency under solar and UV light. 
461 |t Catalysts 
463 |t Vol. 10, iss. 8  |v [847, 27 p.]  |d 2020 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a nano-photo catalysts 
610 1 |a pyrolysis 
610 1 |a holding time 
610 1 |a band gap 
610 1 |a crystal structure 
610 1 |a particle size 
610 1 |a photocatalytic activity 
610 1 |a recombination rate 
610 1 |a фотокатализаторы 
610 1 |a пиролиз 
610 1 |a фотокаталитическая активность 
701 1 |a Massima  |b M. E. S.  |g Mouele Emile Salomon 
701 1 |a Dinu  |b M.  |g Mihaela 
701 1 |a Cummings  |b F.  |g Franscious 
701 1 |a Fatoba  |b O. O.  |g Ojo 
701 1 |a Zar Myint  |b M. T.  |g Myo Tay 
701 1 |a Kyaw  |b H. H.  |g Htet Htet 
701 1 |a Parau  |b A. C.  |g Anca Constantina 
701 1 |a Vladesku  |b A.  |c Romanian specialists in the field of biomaterials  |c researcher of Tomsk Polytechnic University, candidate of biological Sciences  |f 1977-  |g Alina  |3 (RuTPU)RU\TPU\pers\39940 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Исследовательская школа химических и биомедицинских технологий  |b Научно-исследовательский центр "Физическое материаловедение и композитные материалы"  |3 (RuTPU)RU\TPU\col\24957 
801 2 |a RU  |b 63413507  |c 20210413  |g RCR 
856 4 |u https://doi.org/10.3390/catal10080847 
942 |c CF