Wet peroxide oxidation of phenol over carbon/zeolite catalysts. Kinetics and diffusion study in batch and flow reactors

Dades bibliogràfiques
Parent link:Journal of Environmental Chemical Engineering
Vol. 6, iss. 2.— 2018.— [P. 2551-2560]
Autor corporatiu: Национальный исследовательский Томский политехнический университет Инженерная школа природных ресурсов Отделение химической инженерии
Altres autors: Taran O. P. Oxana, Zagoruiko A. N. Andrey Nikolaevich, Yashnik S. A. Svetlana, Ayusheev A. B. Artemiy, Pestunov A. B. Andrey, Prosvirin I. P. Igor, Prihod’ko R. V. Roman, Goncharuk V. V. Vladislav, Parmon V. N. Valentin
Sumari:Title screen
New composite catalysts were synthesized by pyrolysis of carbon-containing compounds supported of Cu-substituted ZSM-5 zeolite. Three series of the catalysts containing 12?wt% of carbon and 1?wt% of copper were prepared (powder, honeycomb monolith and extruded trefoils) and characterized by TEM, XPS, N2 adsorption. Kinetics of catalytic wet peroxide oxidation (CWPO) of phenol was studied in the presence of the composite catalysts using batch and flow reactors. The substrate conversion in the batch reactor was reached 45% in two minutes over the composite catalyst but no more than 8% in five minutes over the zeolite catalyst. Studies of the granulated composites (monoliths and trefoil) in the flow reactor demonstrated a higher efficiency of the trefoil catalyst. The conversion of phenol at the flow rate 20?mL?min?1 was 35% higher over the composite trefoils than over the carbon-free zeolite. The obtained kinetic data allowed the conclusion to be made about different mechanisms of CWPO over zeolite and composite catalysts. The developed kinetic model of phenol CWPO over the composite catalyst described the formation and destruction of intermediate products of phenol oxidation. It was established that inhibiting of phenol oxidation by the substrate was less pronounced in the presence of the composite catalysts than in the presence of the carbon-free catalysts. The flow reactor for phenol oxidation was modeled with account for the external and internal diffusion deceleration of the reaction over real catalyst granules of different geometry to provide adequate description of the experimental results.
Режим доступа: по договору с организацией-держателем ресурса
Idioma:anglès
Publicat: 2018
Matèries:
Accés en línia:https://doi.org/10.1016/j.jece.2018.03.017
Format: Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=658017

MARC

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200 1 |a Wet peroxide oxidation of phenol over carbon/zeolite catalysts. Kinetics and diffusion study in batch and flow reactors  |f O. P. Taran [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 41 tit.] 
330 |a New composite catalysts were synthesized by pyrolysis of carbon-containing compounds supported of Cu-substituted ZSM-5 zeolite. Three series of the catalysts containing 12?wt% of carbon and 1?wt% of copper were prepared (powder, honeycomb monolith and extruded trefoils) and characterized by TEM, XPS, N2 adsorption. Kinetics of catalytic wet peroxide oxidation (CWPO) of phenol was studied in the presence of the composite catalysts using batch and flow reactors. The substrate conversion in the batch reactor was reached 45% in two minutes over the composite catalyst but no more than 8% in five minutes over the zeolite catalyst. Studies of the granulated composites (monoliths and trefoil) in the flow reactor demonstrated a higher efficiency of the trefoil catalyst. The conversion of phenol at the flow rate 20?mL?min?1 was 35% higher over the composite trefoils than over the carbon-free zeolite. The obtained kinetic data allowed the conclusion to be made about different mechanisms of CWPO over zeolite and composite catalysts. The developed kinetic model of phenol CWPO over the composite catalyst described the formation and destruction of intermediate products of phenol oxidation. It was established that inhibiting of phenol oxidation by the substrate was less pronounced in the presence of the composite catalysts than in the presence of the carbon-free catalysts. The flow reactor for phenol oxidation was modeled with account for the external and internal diffusion deceleration of the reaction over real catalyst granules of different geometry to provide adequate description of the experimental results. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Journal of Environmental Chemical Engineering 
463 |t Vol. 6, iss. 2  |v [P. 2551-2560]  |d 2018 
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610 1 |a композиты 
610 1 |a фенолы 
701 1 |a Taran  |b O. P.  |g Oxana 
701 1 |a Zagoruiko  |b A. N.  |c Chemical Engineer  |c Professor of Tomsk Polytechnic University, Doctor of technical sciences  |f 1962-  |g Andrey Nikolaevich  |3 (RuTPU)RU\TPU\pers\33191 
701 1 |a Yashnik  |b S. A.  |g Svetlana 
701 1 |a Ayusheev  |b A. B.  |g Artemiy 
701 1 |a Pestunov  |b A. B.  |g Andrey 
701 1 |a Prosvirin  |b I. P.  |g Igor 
701 1 |a Prihod’ko  |b R. V.  |g Roman 
701 1 |a Goncharuk  |b V. V.  |g Vladislav 
701 1 |a Parmon  |b V. N.  |g Valentin 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Инженерная школа природных ресурсов  |b Отделение химической инженерии  |3 (RuTPU)RU\TPU\col\23513 
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