4.8 Article

Catalytic performance and intermediates identification of trichloroethylene deep oxidation over Ru/3DOM SnO2 catalysts

Journal

JOURNAL OF CATALYSIS
Volume 400, Issue -, Pages 310-324

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2021.06.010

Keywords

Supported ruthenium catalyst; Three-dimensionally ordered macroporous tin oxide; Trichloroethylene oxidation; Chlorine resistance; Reaction intermediate

Funding

  1. National Natural Science Foundation of China [21876006, 21976009]
  2. National Natural Science Committee of China-Liaoning Provincial People's Government Joint Fund [U1908204]
  3. Foundation on the Creative Research Team Construction Promotion Project of Beijing Municipal Institutions [IDHT20190503]
  4. Natural Science Foundation of Beijing Municipal Commission of Education [KM201710005004]
  5. Development Program for the Youth Outstanding-Notch Talent of the Beijing Municipal Commission of Education [CITTCD201904019]

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Ru nanoparticles supported on 3DOM SnO2 exhibited excellent catalytic activity for the oxidation of TCE and/or toluene. The high catalytic performance was attributed to the presence of hydroxyl groups, strong O-2 adsorption ability, low-temperature reducibility, and strong interaction between Ru NPs and 3DOM SnO2. The catalytic mechanism over xRu/3DOM SnO2 under dry and humid conditions was proposed, providing insights for the industrial application of Ru catalysts in the removal of Cl-containing volatile organic compounds.
SnO2 is widely used in catalysis owing to its oxygen vacancies, reducible oxygen species, and acidity. In this work, Ru nanoparticles (NPs) supported on three-dimensionally ordered macroporous (3DOM) SnO2 (xRu/3DOM SnO2, Ru loading (x) = 0.09-1.65 wt%) were fabricated via the polyvinyl alcohol-protected reduction routes, and their catalytic activities were determined for trichloroethylene (TCE) and/or toluene oxidation. It was shown that the 0.98Ru/3DOM SnO2 sample exhibited the best activity and good thermal stability, with the temperature (T-90%) and apparent activation energy at a TCE (1000 ppmv) conversion of 90% being 300 degrees C and 44 kJ/mol at space velocity = 40,000 mL/(g h), respectively. Trichloromethane, carbon tetrachloride, tetrachloroethylene, and trichloroacetaldehyde hydrate were the main intermediates in TCE oxidation. The high catalytic performance of 0.98Ru/3DOM SnO2 was attributed to the presence of hydroxyl groups adsorbed at the oxygen vacancies, strong O-2 adsorption ability, good low-temperature reducibility, and strong interaction between Ru NPs and 3DOM SnO2. In addition, a catalytic mechanism over xRu/3DOM SnO2 was proposed under dry and humid conditions. The introduction of H2O could block some of the reaction pathways from inhibiting the production of C2Cl4, reduce formation of some by-products (e.g., CH2Cl2, CH3COOH, and C2H2Cl2), promote removal of the chlorine species, and generate a greater amount of HCl and a smaller amount of Cl-2. Furthermore, introducing toluene into the TCE stream could generate smaller amounts of organic chlorine by-products and greater amounts of inorganic chlorine products (HCl and Cl-2). We are sure that this work can provide a guideline for the industrial application of supported Ru catalysts in the removal of Cl-containing volatile organic compounds. (C) 2021 Elsevier Inc. All rights reserved.

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