同时脱除烟气中SO2 /NO的单体改造

Kiman Silas
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引用次数: 0

摘要

侵略性酸处理在吸附剂表面产生了丰富的含氧官能团(-OH, C=O, C-O),并作为催化剂载体的结合位点,因此,在本研究中,单体(ACM)表面通过酸改性和高温活化被氧化。各类型催化剂的前驱体由硝酸铈(CeO2 /ACM)、硝酸铜(CuO/ACM)和硝酸钴(Co3 O4 /ACM)采用沉积沉淀法合成。在固定床反应器中,通过燃煤烟气流对催化剂活性进行了研究。SO2 /NOx的突破性研究和实验结果表明,CeO2 /ACM催化剂对NOx的吸附量分别为24.3和18.5 mg/g, CuO/ACM催化剂对NOx的吸附量分别为27.0和32.8mg/g, Co3 O4 /ACM催化剂对NOx的吸附量分别为10.6和49.7mg/g。FTIR、BET和FESEM分析。本研究描述了高效吸附剂在烟气处理中的发展。
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Modification of Monolith for Simultaneous SO2 /NO x Removal from Flue Gas
The aggressive acid treatment creates a wealth of oxygen-containing functional groups (-OH, C=O, C-O) on the surface of an adsorbent and acts as binding sites for catalyst support therefore, in this study, the surface of monolith (ACM) was oxidized via the acid modification and high temperature activation. Various types of catalysts from the precursors of cerium nitrate (CeO2 /ACM), copper nitrate (CuO/ACM) and cobalt nitrate (Co3 O4 /ACM) using the deposition precipitation synthesis method. The catalyst activity tests were investigated in a fixed bed reactor by passing a stream of flue gas generated by burning coal. The breakthrough study of SO2 /NOx and the experimental results showed that for CeO2 /ACM catalyst the adsorption capacity of SO2 was 24.3 and 18.5 mg/g for NOx and for CuO/ACM catalyst they were 27.0 and 32.8mg/g and for Co3 O4 /ACM catalyst, values obtained were 10.6 and 49.7mg/g. FTIR, BET and FESEM analysis were performed. This investigation depicts the development of highly efficient adsorbent for flue gas treatment.
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