CAJ | 학술논문

采用共沉淀法制备了高Co含量的Co/SiO2费托合成催化剂,并向其中添加一定含量的间苯二酚-甲醛树脂凝胶,结果表明,催化剂在393 K干燥时,树脂会发生分解,因而仅有少量的含碳凝胶残留在催化剂中.然而,少量碳凝胶的存在显著增加了催化剂的还原度和金属钴的分散度,致使催化剂表面产生更多的活性金属Co,同时,催化剂的孔径也有所增大,因此Co/SiO2催化剂具有更高的反应活性及高碳烃选择性.其中80％Co/SiO2-C催化剂活性及高碳烃的选择性与我们前期报道的一种高活性的80％Co-8％ZrO2/SiO2催化剂相近.
채용공침정법제비료고Co함량적Co/SiO2비탁합성최화제,병향기중첨가일정함량적간분이분-갑철수지응효,결과표명,최화제재393 K간조시,수지회발생분해,인이부유소량적함탄응효잔류재최화제중.연이,소량탄응효적존재현저증가료최화제적환원도화금속고적분산도,치사최화제표면산생경다적활성금속Co,동시,최화제적공경야유소증대,인차Co/SiO2최화제구유경고적반응활성급고탄경선택성.기중80％Co/SiO2-C최화제활성급고탄경적선택성여아문전기보도적일충고활성적80％Co-8％ZrO2/SiO2최화제상근.
Highly loaded Co/SiO2 catalysts were prepared by the co-precipitation method with resorcinol formaldehyde resin gel (RFG).Most RFG was decomposed during the drying process at 393 K,and little carbon was remained in the catalysts.However,the presence of RFG during the precipitation played the important roles in increasing the pore sizes of catalysts and the reducibility and dispersion of supported cobalt,leading to the more surface active cobalt sites and large pores of the catalysts and therefore the higher activity for the Fischer-Tropsch reactions to produce heavy hydrocarbons.The catalyst 80％Co/SiO2-C thus prepared was as active and selective as the 80％Co-8％ZrO2/SiO2 (an excellent catalyst reported previously) for the synthesis of heavy hydrocarbons from syngas.