Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous Abstract"Inducible overexpression of a rice allene oxide synthase gene increases the endogenous jasmonic acid level, PR gene expression, and host resistance to fungal infection"    Next AbstractHigh-CO(2) Modified Atmosphere Packaging with Superchilling (-1.3 ( degrees )C) Inhibit Biochemical and Flavor Changes in Turbot (Scophthalmus maximus) during Storage »

J Colloid Interface Sci


Title:"Catalytic oxidation of dibromomethane over Ti-modified Co(3)O(4) catalysts: Structure, activity and mechanism"
Author(s):Mei J; Huang W; Qu Z; Hu X; Yan N;
Address:"School of Environmental Science and Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, PR China. School of Environmental Science and Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, PR China. Electronic address: nqyan@sjtu.edu.cn"
Journal Title:J Colloid Interface Sci
Year:2017
Volume:20170623
Issue:
Page Number:870 - 883
DOI: 10.1016/j.jcis.2017.06.077
ISSN/ISBN:1095-7103 (Electronic) 0021-9797 (Linking)
Abstract:"Ti-modified Co(3)O(4) catalysts with various Co/Ti ratios were synthesized using the co-precipitation method and were used in catalytic oxidation of dibromomethane (CH(2)Br(2)), which was selected as the model molecule for brominated volatile organic compounds (BVOCs). Addition of Ti distorted the crystal structure and led to the formation of a Co-O-Ti solid solution. Co(4)Ti(1) (Co/Ti molar ratio was 4) achieved higher catalytic activity with a T(90) (the temperature needed for 90% conversion) of approximately 245 degrees C for CH(2)Br(2) oxidation and higher selectivity to CO(2) at a low temperature than the other investigated catalysts. In addition, Co(4)Ti(1) was stable for at least 30h at 500ppm CH(2)Br(2), 0 or 2vol% H(2)O, 0 or 500ppm p-xylene (PX), and 10% O(2) at a gas hourly space velocity of 60,000h(-1). The final products were CO(x), Br(2), and HBr, without the formation of other Br-containing organic byproducts. The high catalytic activity was attributed to the high Co(3+)/Co(2+) ratio and high surface acidity. Additionally, the synergistic effect of Co and Ti made it superior for CH(2)Br(2) oxidation. Furthermore, based on the analysis of products and in situ DRIFTs studies, a receivable reaction mechanism for CH(2)Br(2) oxidation over Ti-modified Co(3)O(4) catalysts was proposed"
Keywords:Catalytic oxidation Cobalt Dibromomethane (CH(2)Br(2)) Titania;
Notes:"PubMed-not-MEDLINEMei, Jian Huang, Wenjun Qu, Zan Hu, Xiaofang Yan, Naiqiang eng 2017/07/04 J Colloid Interface Sci. 2017 Nov 1; 505:870-883. doi: 10.1016/j.jcis.2017.06.077. Epub 2017 Jun 23"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 16-11-2024