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DEACTIVATION AND COMPOUND FORMATION IN SULFURIC ACID CATALYSTS AND MODEL SYSTEMS

机译:硫酸催化剂和模型系统的失活和化合物形成

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The catalytic deactivation and the simultaneous formation of compounds in industrial sulfuric acid catalysts and their molten salt-gas model systems M(2)S(2)O(7)/V2O5-SO2/O-2/SO3/N-2 (M = Na, K, Cs) have been studied by combined activity measurements and in situ ESR spectroscopy at temperatures up to 500 degrees C. The applied gas compositions were unconverted, and 50 and 90% preconverted standard feed gas containing 10% SO2, 11% O-2, and 79% N-2. This covers the conditions of all beds in an industrial SO2 converter, without interstage absorption of SO3. The temperature of deactivation was shown to decrease with increased degree of preconversion of the feed gas, increased mixing of the alkali promoters, and decreased vanadium content in the catalysts and model systems. The precipitation of V(II), V(IV), and mixed valence V(IV)-V(V) compounds was observed below the onset temperature of the catalyst deactivation. The salts have been isolated under operating conditions from model melts and identified by microscopy and spectroscopic methods. The V(IV) compounds were characterized by ESR spectroscopy and their temperature of decomposition was found to be in the range 450-500 degrees C. Based on the characteristic ESR spectra, the V(IV) compounds causing the deactivation of working industrial catalysts could be identified in situ. Finally it was found that the restoration of deactivated catalysts requires heating to around 500 degrees C, where the low-valence vanadium compounds decompose and reoxidize to V(V). (C) 1995 Academic Press, Inc. [References: 46]
机译:工业硫酸催化剂及其熔融盐气模型系统M(2)S(2)O(7)/ V2O5-SO2 / O-2 / SO3 / N-2(M的催化失活和同时形成化合物通过在高达500摄氏度的温度下通过联合活性测量和原位ESR光谱研究了Na,K,Cs)。 O-2和79%N-2。这涵盖了工业SO2转化器中所有床的条件,而没有阶段间吸收SO3。失活温度显示出随着进料气的预转化程度的增加,碱促进剂的混合的增加以及催化剂和模型系统中钒含量的降低而降低。在催化剂失活的起始温度以下,观察到V(II),V(IV)和化合价V(IV)-V(V)化合物的沉淀。在操作条件下已从模型熔体中分离出盐,并通过显微镜和光谱法鉴定。通过ESR光谱对V(IV)化合物进行表征,发现其分解温度为450-500摄氏度。基于ESR的特征光谱,引起工作中的工业催化剂失活的V(IV)化合物可以被原地识别。最后,发现失活催化剂的还原需要加热到约500摄氏度,在此低价钒化合物分解并重新氧化为V(V)。 (C)1995 Academic Press,Inc. [参考:46]

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