无机化学学报
無機化學學報
무궤화학학보
JOURNAL OF INORGANIC CHEMISTRY
2006年
11期
1933-1940
,共8页
介孔分子筛SBA-15%有机钛金属催化剂%纳米聚乙烯纤维%非均相催化%烯烃聚合
介孔分子篩SBA-15%有機鈦金屬催化劑%納米聚乙烯纖維%非均相催化%烯烴聚閤
개공분자사SBA-15%유궤태금속최화제%납미취을희섬유%비균상최화%희경취합
mesoporous zeolite%SBA-15%titanium%catalyst%heterogenization%nanofibrous polyethylene
通过介孔分子筛SBA-15负载半夹心结构有机金属钛(IV)催化剂在一定的反应温度(20~80℃)和1013 kPa乙烯压力下合成了纳米聚乙烯纤维.讨论并比较了负载剂和聚合条件对催化活性、聚合物分子量及聚合物形态的影响.相对于均相催化剂而言,催化活性有所降低,但聚合物分子量明显增大,达到106数量级.在相同压力下,从低温到高温,聚乙烯形态也从细小纤维束逐渐变粗,更高温度熔成片状,80℃以上纤维状形态消失.这些表明,通过外部条件的选择可以得到合适的聚乙烯纤维.
通過介孔分子篩SBA-15負載半夾心結構有機金屬鈦(IV)催化劑在一定的反應溫度(20~80℃)和1013 kPa乙烯壓力下閤成瞭納米聚乙烯纖維.討論併比較瞭負載劑和聚閤條件對催化活性、聚閤物分子量及聚閤物形態的影響.相對于均相催化劑而言,催化活性有所降低,但聚閤物分子量明顯增大,達到106數量級.在相同壓力下,從低溫到高溫,聚乙烯形態也從細小纖維束逐漸變粗,更高溫度鎔成片狀,80℃以上纖維狀形態消失.這些錶明,通過外部條件的選擇可以得到閤適的聚乙烯纖維.
통과개공분자사SBA-15부재반협심결구유궤금속태(IV)최화제재일정적반응온도(20~80℃)화1013 kPa을희압력하합성료납미취을희섬유.토론병비교료부재제화취합조건대최화활성、취합물분자량급취합물형태적영향.상대우균상최화제이언,최화활성유소강저,단취합물분자량명현증대,체도106수량급.재상동압력하,종저온도고온,취을희형태야종세소섬유속축점변조,경고온도용성편상,80℃이상섬유상형태소실.저사표명,통과외부조건적선택가이득도합괄적취을희섬유.
Nanofibrous polyethylene (PE) was prepared via in situ ethylene extrusion polymerization on SBA-15supported titanium(Ⅳ) cyclopentadienyl-aryloxy catalyst under appropriate reaction temperature (20~80 ℃) and ethylene pressure (1013 kPa). The effects of catalyst support and polymerization conditions on catalyst activity,molecular weight and morphology of polymer were investigated. Compared with homogeneous counterpart, the supported catalyst gave a little lower activity, but very high molecular weight (106) polymers were obtained. At lower temperature, the fine PE fibers were displayed. As the polymerization temperature rose, the resultant fiber bundles got thicker,and then gradually congregated into sheet polymers at higher temperature. Above approximate 80 ℃, the fiber morphologies of the polymers disappeared. These changes indicate that morphology of polymers can be regulated by extrinsic factors.