文献类型：期刊文献

英文题名：The stabilizing effect of water and high reaction temperatures on the CeO2-catalyst in the harsh HCl oxidation reaction

作者：Li, Chenwei[1,2];Hess, Franziska[2,3];Djerdj, Igor[4];Chai, Guangtao[1];Sun, Yu[1,2];Guo, Yanglong[1];Smarsly, Bernd M.[2];Over, Herbert[2]

机构：[1]East China Univ Sci & Technol, Sch Chem & Mol Engn, Res Inst Ind Catalysis, Key Lab Adv Mat, Shanghai 200237, Peoples R China;[2]Justus Liebig Univ, Phys Chem Inst, Heinrich Buff Ring 17, D-35392 Giessen, Germany;[3]MIT, Dept Nucl Sci & Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA;[4]Josip Juraj Strossmayer Univ Osijek, Dept Chem, Cara Hadrijana 8-A, HR-31000 Osijek, Croatia

年份：2018

卷号：357

起止页码：257

外文期刊名：JOURNAL OF CATALYSIS

收录：;EI(收录号：20174904495364);WOS:【SCI-EXPANDED(收录号:WOS:000424172500027)】；

基金：This work was supported by the National Key Research and Development Program of China (2016YFC0204300), National Natural Science Foundation of China (21577035), Commission of Science and Technology of Shanghai Municipality (13521103402, 15DZ1205305) and 111 Project (B08021). Chenwei Li gratefully acknowledges the China Scholarship Council for the Joint-Ph.D program between the China Scholarship Council and the Physikalisch-Chemisches Institut of the Justus-Liebig-University Giessen. We acknowledge financial support by the LOEWE program STORE-E within the Laboratory of Materials Research at the JLU.

语种：英文

外文关键词：Deacon process; CeO2 nanocubes; Stability; Process parameters; Promotion by water

摘要：We studied the stability of CeO2 nano-cubes with preferentially (1 0 0)-oriented facets in the HCl oxidation reaction (Deacon process) for various reaction temperatures and the addition of small concentrations of water in the gas feed. For a reaction mixture HCl:O-2 = 1:2 we find that CeO2 is substantially chlorinated below 380 degrees C, revealing a low catalytic activity. At 390 degrees C both the activity and the chlorination degree change abruptly: activity becomes high and chlorination is not detectable by XRD. The experimental results are rationalized by a kinetic model which allows us to study catalyst chlorination as a function of temperature and gas feed composition. The model predicts that chlorination sets in at the inlet of the catalyst bed and propagates then slowly along the catalyst bed towards the reactor outlet to fully chlorinate the CeO2 catalyst bed. This process has been confirmed by a dedicated experiment employing two separate catalyst layers, where only the first layer is shown to be chlorinated while exposed to the Deacon gas feed. Our model attributes the excessive chlorination at the reactor inlet to the absence of H2O in the gas feed, as the formation of H2O by the reaction of HCl with CeO2 is the prevailing driving force for catalyst chlorination. When running the Deacon process at 375 degrees C, the chlorination of CeO2 nano-cubes is efficiently suppressed by the addition of 1% water to the reaction mixture. This extrinsic stabilization of oxide catalysts towards chlorination by water is a general concept, which may enable the identification of new oxide materials that have previously been ruled out as Deacon catalysts due to their low stability under reaction conditions. (C) 2017 Elsevier Inc. All rights reserved.