钴改性的铁磁性氧化物担载的铑催化剂上双环戊二烯氢甲酰化反应的研究  

Hydroformylation of dicyclopentadiene over Co-Rh/Fe_3O_4 catalyst

作　　者：郝涛 马昱博[1,2,3] 

机构地区：[1]新疆中泰化学,新疆乌鲁木齐830026 [2]中泰化学博士后工作站,新疆乌鲁木齐830026 [3]中国科学院新疆理化技术研究所,新疆乌鲁木齐830026

出　　处：《天然气化工—C1化学与化工》2016年第1期37-40,共4页Natural Gas Chemical Industry

基　　金：中泰化学博士后工作站资助项目

摘　　要：以三氯化铑、硝酸钴和硝酸铁为原料,碳酸钠为沉淀剂,采用共沉淀法制备了不同担载量的钴改性的铁磁性氧化物担载的铑催化剂,并进行了TPR,TPD和TG-DTA等方面的表征,测试了其双环戊二烯(DCPD)氢甲酰化合成三环癸烷二甲醛(DFTD)的催化性能。结果表明,Rh/Fe_3O_4催化剂加入钴后,改善了Rh还原性和分散性,提高了DFTD的选择性。4Co-2Rh/Fe_3O_4催化剂的DFTD选择性最高,达90.6%,而Rh/Fe_3O_4催化剂仅为21.3%。所有催化剂DCPD转化率都可达100%。催化性能的改进可能是在表面生成了反应性能更高的Rh物种。A series of Co-Rh/Fe3O4 catalysts with different Co loading were prepared by co-precipitation method with RhC（l3）,Co（NO3）2and Fe（NO3）3as materials and Na2CO3 as precipitant, and characterized by TPR, TPD and TG-DTA techniques, while their catalytic performances for hydroformylation of dicyclopentadiene（DCPD） to diformyltricyclodecanes（DFTD） were investigated. The results showed that adding Co to Rh/Fe3O4 catalyst could improve Rh reduction and dispersion, resulting in the increase of DFTD selectivity. The 4Co-2Rh/Fe3O4 had the highest value of DFTD selectivity of 90.6%, which was only 21.3% for Rh/Fe3O4. The conversion of DCPD could reach 100% for all catalysts. The improvement of catalytic performance was likely attributed to the formation of a more reactive Rh species on the surface of catalyst.

关 键 词：双环戊二烯 氢甲酰化 三环癸烷二甲醛 Co-Rh/Fe3O4催化剂 

分 类 号：O643[理学—物理化学] TQ426[理学—化学]