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CVOCs在Co基催化剂上的催化燃烧:Ru抑制脱附副产物、CePO4抑制多氯副产物

已有 1403 次阅读 2023-6-24 13:49 |个人分类:科研点滴启发|系统分类:论文交流

https://doi.org/10.1016/j.fuel.2023.129005


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Highlights

  • Nanorods assembled monoclinic CePO4 microspheres was synthesized by a hydrothermal method using trimethyl phosphate.

  • RuCoOx/CePO4 demonstrated outstanding selectivity, durability and thermal stability for catalytic oxidation of 1,2-dichloroethane.

  • Abundant acidic and electron-withdrawing CePO4 contributed to inhibition of polychlorinated byproducts.

  • RuO2 enhanced redox ability and migration of lattice oxygen thus suppressed generation of dechlorinated byproducts.

Abstract

Highly toxic, reactive and refractory chlorinated VOCs (Cl-VOCs) is urgent for purification by the most favoured catalytic oxidation technique, however, the formation of polychlorinated byproducts is huge obstacle for most catalysts. Here, nanorods assembled monoclinic CePO4 microspheres were synthesized and used as the support of highly active but low-selective Co3O4 for catalytic oxidation of Cl-VOCs. The prepared Co3O4/CePO4 using ascorbic acid (AA) as a chelating agent presented a high activity and low selectivity of vinyl chloride (VC) for catalytic oxidation of 1,2-dichloroethane (DCE) due to the high dispersion of Co3O4, compared with bulk Co3O4 and Co3O4/SiO2, possible polychlorinated byproducts were completely inhibited in the presence of CePO4 support. The co-introduction of RuO2 further suppressed the formation of VC as a representative dechlorinated byproduct owing to the enhanced redox ability and migration of surface lattice oxygen, below 0.5% VC selectivity was detected on the optimized RuCoOx/CePO4 and completely disappeared above 275 °C. Moreover, RuCoOx/CePO4 also revealed the superior versatility, durability and thermal stability as well as the outstanding resistance to CO2, H2O and sulfur. The restraint of polychlorinated byproducts also can be achieved by other phosphates besides CePO4 and attributed to the strong coordination effect and electron-withdrawing function of PO43-. This work was contributed to further understand the inhibition of chlorinated byproducts for catalytic oxidation of Cl-VOCs and rationally design full-featured catalysts.



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