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PREPOLYMERIZATION FOR THE GAS PHASE POLYMERIZATION OF PROPYLENE

机译:丙烯气相聚合的预聚合

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Since the development of Ziegler-Natta catalysts in the 1950s, continuous improvements were performed with regard to higher catalyst activity and higher stereo-selectivity. However, especially at the polymerization start, when the pure catalyst is injected under high rate conditions, the high activity of the catalyst may cause particle overheating and/or lead to an uncontrolled catalyst fragmentation resulting in lower catalyst activity and bad particle morphology. One possibility to solve the problem is to apply a prepolymerization step before the main polymerization. In the prepolymerization, the reaction starts at low rate conditions (mild reaction temperatures, low monomer concentration) in order to realize a controlled catalyst fragmentation and to improve heat removal conditions for the main polymerization by creating a higher heat transfer area. The current contribution deals with the prepolymerization of propylene in lab-scale under industrially relevant conditions. The main gas phase polymerization is conducted in a 5 I horizontal stirred tank reactor. Prepolymerization is performed in-situ, meaning in the same reactor by injecting the catalyst at a low initial temperature, or externally in a 250 ml calorimeter. The latter case offers the benefit of controlled prepolymerization conditions with access to prepolymerization kinetics and defined starting conditions for the main polymerization. Experiments were performed for varying reaction conditions. The two prepolymerization methods are compared and the effect of prepolymerization on the activity of the main polymerization is discussed.
机译:自1950年代开发齐格勒-纳塔催化剂以来,就更高的催化剂活性和更高的立体选择性进行了持续改进。然而,特别是在聚合开始时,当在高速率条件下注入纯催化剂时,催化剂的高活性可能导致颗粒过热和/或导致不受控制的催化剂碎裂,从而导致较低的催化剂活性和不良的颗粒形态。解决该问题的一种可能性是在主聚合反应之前进行预聚合步骤。在预聚合中,反应在低速率条件下(温和的反应温度,低的单体浓度)开始,以实现受控的催化剂裂解并通过产生更高的传热面积来改善主聚合的除热条件。目前的贡献涉及在工业相关条件下实验室规模的丙烯预聚合。主气相聚合在5升卧式搅拌釜反应器中进行。预聚合是在原位进行的,这意味着在同一反应器中以较低的初始温度注入催化剂,或从外部以250 ml的热量计进行注入。后一种情况的优点是可控制的预聚合条件,可以达到预聚合动力学和确定主聚合的起始条件。针对不同的反应条件进行了实验。比较了两种预聚合方法,并讨论了预聚合对主聚合活性的影响。

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