内蒙古工业大学学报(自然科学版)
內矇古工業大學學報(自然科學版)
내몽고공업대학학보(자연과학판)
JOURNAL OF INNER MONGOLIA UNIVERSITY OF TECHNOLOGY(NATURAL SCIENCE EDITION)
2013年
3期
189-193
,共5页
姜浩强%何润霞%武芳%智科端%周晨亮%张万华%刘全生
薑浩彊%何潤霞%武芳%智科耑%週晨亮%張萬華%劉全生
강호강%하윤하%무방%지과단%주신량%장만화%류전생
高温水煤气变换%铁基催化剂%阴离子环境%活性
高溫水煤氣變換%鐵基催化劑%陰離子環境%活性
고온수매기변환%철기최화제%음리자배경%활성
High temperature shift%Fe-based catalyst%Anion types%Activity
采用湿法共沉淀工艺制备了不同阴离子环境下的铁基高温变换催化剂,利用XRD、BET、TG-DTA、TEM和活性测试等对催化剂样品的结构和性能进行比较研究。结果表明,阴离子环境对催化剂制备过程中所生成前驱体的结构影响较大,最终导致成品催化剂性能相差很大。 SO2-4环境下制备的催化剂活性较好,500℃耐热180min后350℃的活性可达24.52%,而Cl -环境下制备的催化剂活性较差,500℃耐热后350℃的活性为6.94%。
採用濕法共沉澱工藝製備瞭不同陰離子環境下的鐵基高溫變換催化劑,利用XRD、BET、TG-DTA、TEM和活性測試等對催化劑樣品的結構和性能進行比較研究。結果錶明,陰離子環境對催化劑製備過程中所生成前驅體的結構影響較大,最終導緻成品催化劑性能相差很大。 SO2-4環境下製備的催化劑活性較好,500℃耐熱180min後350℃的活性可達24.52%,而Cl -環境下製備的催化劑活性較差,500℃耐熱後350℃的活性為6.94%。
채용습법공침정공예제비료불동음리자배경하적철기고온변환최화제,이용XRD、BET、TG-DTA、TEM화활성측시등대최화제양품적결구화성능진행비교연구。결과표명,음리자배경대최화제제비과정중소생성전구체적결구영향교대,최종도치성품최화제성능상차흔대。 SO2-4배경하제비적최화제활성교호,500℃내열180min후350℃적활성가체24.52%,이Cl -배경하제비적최화제활성교차,500℃내열후350℃적활성위6.94%。
The Fe -based high temperature shift catalysts were prepared by the wet co -precipitation method, which were characterized by XRD , SBET and TG-DTA and tested for water-gas shift reaction.The results showed that anions types had significant effects on the structure and performance of precursor which generated during the process of preparation , finally caused product catalyst performance vary widely .The catalytic activity of sample in the SO 2-4 environment was better , which was 24 .52% at 350℃ after heat resistance(500℃,180min);the catalytic activity of sample in the Cl -environment was lower, which was 6. 94%at 350℃after heating resistance(500℃,180min).