Catalytic Activity During the Preparation of PE/Clay Nanocomposites by In Situ Polymerization with Metallocene Catalysts

被引:29
作者
Zapata, Paula [1 ,2 ]
Quijada, Raul [1 ,2 ]
Covarrubias, Cristian [1 ,2 ]
Moncada, Edwin [3 ]
Retuert, Jaime [1 ,2 ]
机构
[1] Univ Chile, Fac Ciencias Fis & Matemat, Dept Ingn Civil Quim & Biotecnol, Santiago 861, Chile
[2] Ctr Invest Interdisciplinaria Avanzada Ciencia Ma, Santiago 861, Chile
[3] Ciencia Polimeros BRASKEM A III Polo Petroquim, BR-95853000 Passo Raso Triunfo, RS, Brazil
关键词
ethylene polymerization; metallocene catalyst; polyolefin nanocomposites; clays; POLYETHYLENE/MONTMORILLONITE NANOCOMPOSITES; MONTMORILLONITE NANOCOMPOSITES; ETHYLENE POLYMERIZATION; ZIRCONOCENE CATALYSTS; SUPPORTED CATALYST; COPOLYMERIZATION; POLYPROPYLENE; TEMPERATURE; SILICATE; ACID;
D O I
10.1002/app.30334
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Catalytic activity during the formation of polyethylene (PE)/clay nanocomposites by in situ polymerization with metallocenes was studied. Ethylene polymerization was carried out with the homogeneous metallocene in the presence of the clay particles and using the clay-supported metallocene catalyst. It was found that the catalytic activity of the homogeneous metallocene does not decrease in the presence of the clay particles and only a slight decrease of activity occurs using the clay-supported catalyst. The modification of the clay with MAO cocatalyst as well as its intercalation with ODA surfactant were found to play an important role during the in situ formation of the PE/clay nanocomposite. ODA-intercalated clay apparently facilitates the activation and monomer insertion processes on zirconocene centers located in internal sites of the clay structure. Although metallocene supported on MAO-treated clay exhibited somewhat lower catalytic activity than that supported directly on the ODA-intercalated clay, both systems favored the production of PE nanocomposites containing highly exfoliated clay particles. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 113: 2368-2377, 2009
引用
收藏
页码:2368 / 2377
页数:10
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