کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
40203 45845 2014 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A study of the formation process of titanium–magnesium catalyst for propylene polymerization
ترجمه فارسی عنوان
مطالعه فرآیند تشکیل کاتالیزور تیتانیوم منیزیم برای پلیمریزاسیون پروپیلن
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
چکیده انگلیسی


• Catalyst formation by reacting Mg(OEt)2 with TiCl4 and dibutylphthalate (DBP) is studied.
• Without DBP the X-ray amorphous product consisting of MgCl2 and TiCl3(OEt) is formed.
• This product has very high SBET (over 400 m2/g) but low activity and low stereospecificity.
• DBP use leads to removing TiCl3(OEt), forming MgCl2 crystallites, entering DBP and TiCl4.
• TiCl4/ChB treating of solid product completes these processes increasing activity and stereospecificity.

The catalyst formation by reacting magnesium diethoxide with titanium tetrachloride in the presence of stereoregulating electron donor – di-n-butylphthalate (DBP) – is studied by sampling the intermediate products during catalyst synthesis. Chemical and phase composition, porous structure, activity and stereospecificity of these products are investigated. It is show that before DBP adding the X-ray amorphous product consisting of MgCl2 and TiCl3(OEt) is formed. This product has micro-mesoporous structure, very high surface area, but low activity and low stereospecificity. DBP has a significant effect on both the chemical composition of the catalyst due to removing inactive TiCl3(OEt), entering DBP and TiCl4 in solid product and formation of MgCl2 crystallites with mesoporous structure. At the same time the significant increase of the activity and stereospecificity is observed. Following TiCl4/chlorobenzene treatment of solid product completes these processes, provides some increasing the surface area at similar mesoporous structure and additionally increases activity and stereospecificity.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 469, 17 January 2014, Pages 512–516
نویسندگان
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