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    • 1. 发明授权
    • α-Olefin polymer and process for production thereof
    • α-烯烃聚合物及其生产方法
    • US08178635B2
    • 2012-05-15
    • US12526978
    • 2008-02-18
    • Takenori FujimuraMasami KanamaruYutaka MinamiTakuji Okamoto
    • Takenori FujimuraMasami KanamaruYutaka MinamiTakuji Okamoto
    • C08F4/64C08F4/76C08F10/14C08F10/00
    • C08F10/14C08F4/65908C08F4/65912C08F110/14C08F210/14Y10S526/904Y10S526/941Y10S526/943C08F4/65927C08F4/6492C08F2500/20C08F2500/03C08F2500/02C08F2500/17
    • Provided is an α-olefin polymer having an excellent balance between a molecular weight and a melting point, which is a polymer of one or more kinds of α-olefins having 20 to 40 carbon atoms, and which meets the following requirements (1) to (4): (1) the α-olefin polymer has a molecular weight distribution (Mw/Mn) determined from its weight average molecular weight (Mw) and number average molecular weight (Mn) in terms of polystyrene measured by a GPC method of 2 or less, and has an Mw of 5,000 or less; (2) measurement of a melting point (Tm) of the α-olefin polymer with DSC shows one melting peak, a melting heat absorption (AH) calculated from an area of the melting peak is 20 J/g or more, and the melting peak has a half value width of 10° C. or less; (3) when the Mw falls within a range of 1,000 to 5,000 and an average number of carbon atoms (Cn) of the α-olefins falls within a range of 20 to 40, the Mw, the Cn, and the Tm measured with the DSC satisfy the relationship, 0.0025×Mw+(Cn×3.3812−29.5)≦Tm≦0.0025×Mw+((Cn+1)×3.3812−29.5); and (4) a stereoregularity index [M2] derived from a chain of the α-olefins each having 20 to 40 carbon atoms is 20% by mol or more.
    • 本发明提供一种具有20〜40个碳原子的一种以上的α-烯烃的分子量和熔点之间的平衡优异的α-烯烃聚合物,其满足以下要求(1)〜 (4):(1)α-烯烃聚合物的重均分子量(Mw)和数均分子量(Mn)的聚苯乙烯的分子量分布(Mw / Mn) 2以下,Mw为5000以下; (2)通过DSC测定α-烯烃聚合物的熔点(Tm),显示出一个熔融峰,由熔融峰面积计算出的熔融热吸收(AH)为20J / g以上,熔融 峰值的半值宽度为10℃以下; (3)当Mw落在1,000〜5000的范围内时,α-烯烃的平均碳原子数(Cn)在20〜40的范围内,使用以下方法测定的Mw,Cn和Tm DSC满足关系:0.0025×Mw +(Cn×3.3812-29.5)≦̸ Tm≦̸ 0.0025×Mw +((Cn + 1)×3.3812-29.5); 和(4)来自各自具有20〜40个碳原子的α-烯烃的链的立构规整性指数[M2]为20摩尔%以上。
    • 7. 发明申请
    • Olefin polymerization process
    • 烯烃聚合工艺
    • US20060160962A1
    • 2006-07-20
    • US10563497
    • 2004-06-29
    • Maria TontiMarkus OberhoffVolker FraaijeBernd Bachmann
    • Maria TontiMarkus OberhoffVolker FraaijeBernd Bachmann
    • C08F2/00
    • C08F110/06C08F4/65912C08F4/65916Y10S526/904Y10S526/905C08F4/65927C08F2/06
    • A process for polymerizing one or more alpha-olefins of formula CH2═CHT wherein T is a hydrogen atom or a C1-C20 alkyl radical comprising the following steps: a) contacting in a continuous way one or more of said alpha olefins with a metallocene based catalyst system in a loop reactor, wherein: (i) the reaction is carried out in a liquid medium; (ii) the average residence time of the metallocene-based catalyst system is not more than 30 minutes; (iii) the temperature of the loop ranges from 25° to 70° C.; in to obtain a polymerization degree ranging from 60 to 500 g per gram of catalyst system; b) feeding in continuous the prepolymerized metallocene-based catalyst system obtained in step a) into a polymerization reactor C) polymerizing one or more alpha-olefins, the same or different from the alpha olefins used in step a), in the presence of said prepolymerized metallocene-based catalyst system.
    • 用于聚合一种或多种式CH 2 -CHT的α-烯烃的方法,其中T是氢原子或C 1 -C 20 - 烷基,其包括以下步骤:a)在环流反应器中以连续方式使一种或多种所述α-烯烃与茂金属基催化剂体系接触,其中:(i)反应在液体介质中进行; (ii)金属茂系催化剂体系的平均停留时间不超过30分钟; (iii)环路温度为25°至70°C; 以获得每克催化剂体系60至500克的聚合度; b)将在步骤a)中获得的预聚合的茂金属基催化剂体系连续进料到聚合反应器中C)使所述α-烯烃在所述 预聚金属茂系催化剂体系。
    • 9. 发明授权
    • Process for preparing a highly active metallocene catalyst supported on polymer bead for olefin polymerization
    • 制备负载于聚合物珠粒上用于烯烃聚合的高活性金属茂催化剂的方法
    • US06677412B2
    • 2004-01-13
    • US10118617
    • 2002-04-02
    • Son-Ki IhmKi-Soo LeeO-Yong Jeong
    • Son-Ki IhmKi-Soo LeeO-Yong Jeong
    • C08F444
    • C08F10/02C08F4/65912C08F4/6592C08F110/02Y10S502/507Y10S526/904C08F4/65916
    • The present invention relates to a process for preparing a highly active metallocene catalyst supported on polymer bead for olefin polymerization, a metallocene catalyst prepared by the said process and a method for alkylene polymerization by employing the said catalyst. The process for preparing a highly active metallocene catalyst supported on polymer bead for olefin polymerization which comprises the steps of: dissolving divinylbenzene, vinylbenzylchloride, and an initiator in an organic solvent, mixing it with a suspension stabilizer of aqueous phase, and carrying out suspension-polymerization at the temperature of 40 to 80° C. to obtain polystyrene; swelling the polystyrene in dialcoholamine dissolved in an organic solvent at ambient temperature for 1 to 3 days, to give a polymer having a functional group of dialcoholamine; and, reacting the polymer with a metallocene compound (CpM*Cl3) dissolved in an organic solvent. The metallocene catalyst of the present invention can be used widely for ethylene polymerization, styrene polymerization and copolymerization, while replacing the conventional homogeneous catalysts.
    • 本发明涉及一种负载在用于烯烃聚合的聚合物珠上的高活性茂金属催化剂的方法,通过所述方法制备的茂金属催化剂和通过使用所述催化剂进行亚烷基聚合的方法。 制备负载在用于烯烃聚合的聚合物珠子上的高活性金属茂催化剂的方法,该方法包括以下步骤:将二乙烯基苯,乙烯基苄基氯和引发剂溶解在有机溶剂中,将其与水相的悬浮稳定剂混合, 在40〜80℃的温度下进行聚合,得到聚苯乙烯; 在环境温度下溶解在有机溶剂中的二元醇胺中使聚苯乙烯溶胀1至3天,得到具有二醇胺官能团的聚合物; 并使聚合物与溶解在有机溶剂中的茂金属化合物(CpM * Cl3)反应。 本发明的茂金属催化剂可以广泛用于乙烯聚合,苯乙烯聚合和共聚,同时代替常规的均相催化剂。