化学世界
化學世界
화학세계
CHEMICAL WORLD
2009年
12期
724-726,730
,共4页
于部伟%王斯晗%张宝军%闫功臣%张婧元%陈谦%赵晶莹
于部偉%王斯晗%張寶軍%閆功臣%張婧元%陳謙%趙晶瑩
우부위%왕사함%장보군%염공신%장청원%진겸%조정형
铁催化剂%乙烯齐聚%α-烯烃
鐵催化劑%乙烯齊聚%α-烯烴
철최화제%을희제취%α-희경
iron catalyst%α-ethylene oligomerization
合成了新型配合物氯化2-乙酰基-6-(2-甲基苯亚胺基)乙基吡啶铁,研究了它与甲基铝氧烷(MAO)、促进剂(1,1,2,2-四氯乙烷)共同组成的三元催化体系催化乙烯齐聚的性能.在40℃、3.0 MPa、n(Al)/n(Fe)=1200、反应时间为30 min,主催化剂浓度为18μmol/L,促进剂用量为0.4ml的条件下,催化剂活性高达3.8×10~6g/mol·h,而且丁烯-1选择性小于10%,己烯-1选择性大于22%,辛烯-1选择性大于23%.
閤成瞭新型配閤物氯化2-乙酰基-6-(2-甲基苯亞胺基)乙基吡啶鐵,研究瞭它與甲基鋁氧烷(MAO)、促進劑(1,1,2,2-四氯乙烷)共同組成的三元催化體繫催化乙烯齊聚的性能.在40℃、3.0 MPa、n(Al)/n(Fe)=1200、反應時間為30 min,主催化劑濃度為18μmol/L,促進劑用量為0.4ml的條件下,催化劑活性高達3.8×10~6g/mol·h,而且丁烯-1選擇性小于10%,己烯-1選擇性大于22%,辛烯-1選擇性大于23%.
합성료신형배합물록화2-을선기-6-(2-갑기분아알기)을기필정철,연구료타여갑기려양완(MAO)、촉진제(1,1,2,2-사록을완)공동조성적삼원최화체계최화을희제취적성능.재40℃、3.0 MPa、n(Al)/n(Fe)=1200、반응시간위30 min,주최화제농도위18μmol/L,촉진제용량위0.4ml적조건하,최화제활성고체3.8×10~6g/mol·h,이차정희-1선택성소우10%,기희-1선택성대우22%,신희-1선택성대우23%.
The new complex Fe(N,N,O)Cl_2(N,N,O=6-[1-{(2-methy)imino)ethyl]-2-acetylpyridine)was prepared and evaluated as precatalyt in the oligomerization of ethylene,using methylaluminoxane (MAO)as cocatalyst and 1,1,2,2-tetrachloroethane as accelerant.The catalytic activities and selectivities of the system in ethylene oligomerization were studied under different reaction temperatures,n(Al)/n(Fe)and reaction pressure.The optimum reaction conditions were as follows:18 μmol/L of catalyst,40℃,3.0 MPa,n(Al)/n(Fe)=1200,reaction time 30 min.0.4 mL accelerant.The activity reached 3.8×10~6 g/mol·h and the selectivity of buterte-1 was less than 10%;where as the selectivities of hexene-1 and octene-1 were more than 22%and 2.3%,respectively.