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1.
二十世纪八十年代,Ishihara等人首次使用钛/甲基铝氧烷(MAO)催化体系成功地制备了间规聚苯乙烯(sPS)[1].此后,由于sPS具有结晶速度快,熔点达270℃,赋予了sPS不同于一般聚苯乙烯的优良性能,因此研制新型的苯乙烯间规聚合催化剂成为国内外的研究热点之一.以往的研究主要集中于催化剂活性的提高,因为单核催化剂只是单一的活性中心,所以只能制备窄分子量分布(MWD)的sPS.近年来,为了提高sPS的加工性能和拓宽sPS的分子量分布,人们使用了不同的茂金属混合物[2,3]或者Z iegler-Natta催化剂的氢化物和单一的茂金属进行了诸多尝试[4,5].至今,…  相似文献   

2.
β-二酮-茂基二氯化钛/MAO催化体系用于苯乙烯间规聚合   总被引:8,自引:0,他引:8  
制备了 β 二酮类配体 [O ,O]的茂基二氯化钛配合物CpTi(dbm)Cl2 .实验证明 ,这类配合物在助催化剂甲基铝氧烷MAO作用下 ,可催化苯乙烯间规聚合 .显示较高的活性 (10 7× 10 5gPS molTi·h) .所得聚合物具有较高的间规度 .CpTi(dbm)Cl2 MAO体系催化活性随铝 钛比的增加呈上升而后衰减 ,当铝 钛比为 5 0 0左右时活性最高 ;聚合温度较高时会导致催化活性下降 .对聚合物进行了1 3C NMR表征  相似文献   

3.
综述了苯乙烯间规聚合主催化剂的研究和开发状况。主要介绍茂、茚、多元稠合环,氟和非茂钛等较高活性催化剂的催化特性,从取代基的电子效应和空间效应以及活性种稳定性等方面阐述了不同催化剂的聚合活性差异。  相似文献   

4.
茂钛催化剂的苯乙烯间规聚合   总被引:12,自引:2,他引:10  
比较了几种庞钛化合物/甲基铝氧烷/三甲基铝均相催化剂的苯乙烯间规聚合,认为茂基三正丙氧基钛[CpTi(O-n-Pr)3]是苯乙烯间规聚合的良好催化剂[催化效率:ωps·ωTi-1=4×104g·g-1].探索了催化剂浓度、单体浓度、聚合温度和时间对苯乙烯聚合的影响.聚合反应产物用佛丁酮萃取,沸丁酮不可溶级分大于95%,经13CNMR分析该级分为间规聚苯乙烯.  相似文献   

5.
β 二酮钛配合物/甲基铝氧烷催化体系用于苯乙烯的间规聚合许学翔谢光华(中国科学院化学研究所北京100080)关键词β 二酮钛配合物,苯乙烯,甲基铝氧烷,间规聚合苯乙烯聚合物可分为无规聚苯乙烯(a PS),等规聚苯乙烯(i PS),间规聚苯乙烯(s?..  相似文献   

6.
对位卤代的苯酚与五甲基茂三氯化钛在三乙胺存在下进行酯化反应 ,制得五甲基茂基三 (对 卤代苯氧基 )钛的 4种新型化合物Cp Ti(O C6 H4 X) 3(X =F ,Cl,Br,I) .用作主催化剂经甲基铝氧烷 (MAO)和三异丁基铝 (TIBA)活化 ,对苯乙烯间规聚合显示出极高的催化活性 ,催化剂热稳定性好 ,制得的聚苯乙烯间规度、分子量和熔点均高 ,在MAO TIBA Ti =4 0 0 2 0 0 1(摩尔比 ) ,温度 6 0℃时 ,10min催化效率可达 3 4 7× 10 6gPS mol·Ti,MAO TIBA Ti=4 0 0 2 0 0 1时茂钛化合物的催化活性几乎是MAO Ti=6 0 0时的 10倍以上 ;4种茂钛催化剂的活性次序Cp Ti(O C6 H4 F) 3 >Cp Ti(O C6 H4 Cl) 3 >Cp Ti(O C6 H4 Br) 3 >Cp Ti(O C6 H4 I) 3 .  相似文献   

7.
茂金属催化剂广泛应用于催化α-烯烃和苯乙烯的定向聚合. 与传统的Ziegler-Natta催化剂相比, 茂金属催化剂催化活性中心单一, 聚合过程立体定向性强, 且往往得到用常规方法所不能得到的新型聚合物[1~5]. Ishihara等[6]首次采用钛金属有机化合物与甲基铝氧烷(MAO)体系催化苯乙烯聚合, 分离得到间规聚苯乙烯, 从此揭开了苯乙烯定向聚合的新篇章, 合成了大量茂金属有机化合物, 用于催化苯乙烯间规聚合, 其中半夹心结构的茂金属化合物CpTiX3[7,8], IndTiCl3[3,4,9,10][Cp=(未)取代环戊二烯基, Ind=(未)取代茚基; X=Cl, F, 烷氧基等]具有最好的催化活性及间规定向性. (CpHMe4)TiF3[8]催化活性高达1.01×108 g PS/(mol Ti*h), 间规度≥95%.  相似文献   

8.
9.
β二酮钛配合物/MAO催化合成间规聚苯乙烯及其热性能   总被引:5,自引:0,他引:5  
间规聚合;β二酮钛配合物/MAO催化合成间规聚苯乙烯及其热性能  相似文献   

10.
苯乙烯间规聚合进展   总被引:1,自引:0,他引:1  
苯乙烯间规聚合在近10年来得到迅速的发展。本文将综述用于苯乙烯间规聚合的催化剂、助催化剂以及聚合机理。  相似文献   

11.
Benzyl cyclopentadienyl titanium trichloride (BzCpTiCl3) was synthesized from benzyl bromide, cyclopentadienyl lithium, and titanium tetrachloride and used in combination with methylaluminoxane (MAO) for the syndiospecific polymerization of styrene. Kinetic measurements of the polymerization were carried out at different temperatures. The polymerization with BzCpTiCl3/MAO differs from the polymerization with cyclopentadienyl titanium trichloride in its behavior toward the Al/Ti ratio. In addition, high activities are observed at high Al/Ti ratios. By analyzing the polymerization runs and the physical properties of the polymers with differential scanning calorimetry, 13C NMR spectroscopy, wide‐angle X‐ray scattering measurements, and gel permeation chromatography, we found that the phenyl ring coordinates to the titanium atom during polymerization. Other known substitutions of the cyclopentadienyl ring (V. Scholz, Dissertation, University of Hamburg, 1998) in principle influence the polymerization activity. The physical properties of the polymers produced by the catalysts already known are nearly identical. BzCpTiCl3 is the first catalyst that leads to polystyrene obviously different from the polystyrene produced by other highly active catalysts. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2805–2812, 2001  相似文献   

12.
CH2?CHCH2CpTiCl3 (1), CH2?CHCH2CH2CpTiCl3 (2) and CH3CH2CH3CpTiCl3 (3) have been synthesized and characterized. The influence of the alkenyl substituent groups on the catalyst activities in the syndiotactic polymerization of styrene was investigated. The catalyst activities decreased in the order CH2?CHCH2CH2CpTiCl3 > CH3CH2CH2CH2CpTiCl3 > CH3CH2CH2CpTiCl3 > CH2?CHCH2CpTiCl3 (Cp?C5H4). By using complex 1, the dependence of the activity on the concentration of methylaluminoxane, triisobutylaluminum and diisobutylaluminum hydride was investigated. Copyright © 2003 John Wiley & Sons, Ltd.  相似文献   

13.
IndTiCl2(OR)/MAO体系催化苯乙烯间规聚合   总被引:1,自引:0,他引:1  
Since Ishihara et al[1] reported that a new macromolecule syndiotact ic polystyrene (s-PS) could be produced with high stereoregularity by using ( η5-Cp)TiCl3 activated with methylaluminoxane (MAO), more efforts were de voted to syntheses of new kinds of half-sandwich titanocenes and to elucidation of the relationship of precursor structure to its catalytic behavior[2~4]. The effect of the substituents attached to π-ligand on the styrene polym erization has been discussed[2~4], but the effect of σ-bonded ligands has not been reported properly.  相似文献   

14.
15.
间规聚苯乙烯的改性研究   总被引:3,自引:0,他引:3  
间规聚苯乙烯(sPS)问世以来,这种新的热塑性聚合物在不同领域的应用得到广泛关注。介绍了sPS的结构与性能,综述了其发展、改性及应用情况。  相似文献   

16.
An on-line electron spin resonance (ESR) technique was applied to investigate the syndiospecific polymerization of styrene activated by the catalyst system CpTiCl3/MMAO. The measurements included trivalent titanocene concentration and monomer conversion. The activation procedure was found to have a dramatic effect on catalyst activity. Adding the reactants in the order of (MMAO + CpTiCl3) + St gave a much higher trivalent titanocene concentration and catalyst activity than the order of (MMAO + St) + CpTiCl3. The catalyst deactivation behaviors in the temperature range of 25–70°C were followed as a function of time during polymerization. At high Al/Ti ratios (500–1000), the decay rates of trivalent titanocene in the presence of styrene were much faster than those of the pure catalyst system. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 3385–3390, 1999  相似文献   

17.
三个新茂钛催化剂的合成及苯乙烯间规聚合   总被引:1,自引:0,他引:1  
合成了三个新茂钛催化剂:茂基三呋喃甲氧基钛,茂基三(四氢呋喃甲氧基)钛,茂基三苄氧基钛,其结构均经元素分析、^1HNMR、^1^3CNMR、IR及MS确证。它们与甲基铝氧烷(MAO)组成的催化体系对苯乙烯间规均聚合有良好的催化活性。  相似文献   

18.
Copolymerization of styrene (St) and St‐terminated poly(ethylene oxide) macromonomer (SEOM) with CpTiCl3/methylaluminoxane (MAO) catalyst in toluene was investigated. The copolymerization of St and SEOM proceeded easily to give a graft copolymer consisting of syndiotactic polystyrene as the main chain and hydrophilic poly(ethylene oxide) as the side chain. A number of side chains in the graft copolymer could be controlled by the amount of SEOM in the feed. The reactivity of SEOM was determined from copolymerization of St and SEOM with the CpTiCl3/MAO catalyst, and the reactivity of SEOM depended on the molecular weight of SEOM. The thermal properties of the graft copolymer such as the melting temperature were influenced by the introduction of SEOM. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2904–2910, 2004  相似文献   

19.
The syndiotactic polystyrene polymerization activity of a fluorinated half‐sandwich complex, η5‐pentamethylcyclopentadienyl titanium trifluoride (Cp*TiF3), in the presence of relatively low amounts of methylalumoxane (MAO; MAO/Cp*TiF3 molar ratio = 200/1) and triisobutylaluminum, is significantly increased by the addition of phenylsilane in molar ratios to Cp*TiF3 ranging from about 300/1 to 600/1, if the phenylsilane is added to the monomer. Lower amounts of phenylsilane, such as a 100/1 molar ratio to Cp*TiF3, lead to a reduced polymerization activity in comparison with styrene without phenylsilane. A prereaction of phenylsilane with the catalyst mixture shows a behavior that is strongly dependent on the storage time of the composition and the temperature. A storage time of about 16 h is sufficient to reduce the polymerization conversion to about half of the original value. The results are discussed on the basis of a chain‐transfer reaction with phenylsilane and several catalyst complexes of different stabilities and activities, including an alkylation product of phenylsilane. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 3476–3485, 2000  相似文献   

20.
以磺化间规聚苯乙烯(SsPS)为增容剂,将间规聚苯乙烯(sPS)和尼龙6/改性蒙脱土纳米复合物(PA6-MTA)共混,得到综合性能优良的新型多组分聚合物/蒙脱土纳米复合材料(sPS/PA6/SsPS/MTA)。用DSC、DMA、WAXD及力学性能测试仪研究了纳米复合材料的结构与性能。TEM测定证明了蒙脱土在基体中的层厚分布为10-50nm。  相似文献   

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