期刊
POLYMERS
卷 15, 期 3, 页码 -出版社
MDPI
DOI: 10.3390/polym15030555
关键词
Ziegler-Natta catalyst; porous organic polymer (POP); isotactic polypropylene; broad molecular weight distribution
POPs-supported Ziegler-Natta catalysts were designed for synthesis of iPP, showing good polymerization activity, high stereoregularity, and broad MWD by adding internal electron donor ID-2. The catalyst exhibited higher chain stereoregularity compared to MgCl2-supported Z-N catalysts with the same internal electron donor.
Porous organic polymers (POPs) have attracted much attention in numerous areas, including catalysis, adsorption and separation. Herein, POP supported Ziegler-Natta catalysts were designed for preparation of isotactic polypropylene (iPP). The POPs-based Ziegler-Natta catalysts exhibited the characteristic of broad molecular weight distribution (MWD > 11) with or without adding an extra internal electron donor. The added internal electron donor 3-methyl-5-tert-butyl-1,2-phenylene dibenzoate (ID-2) used in cat-2 showed good propylene polymerization activity of 15.3 x 10(6) g center dot PP/mol center dot Ti center dot h, high stereoregularity with 98.2% of isotacticity index and broad molecular weight distribution (MWD) of 12.3. Compared to the MgCl2-supported Ziegler-Natta catalysts (cat-4) with the same ID-2, cat-2 showed higher chain stereoregularity for propylene polymerization. As seen in the TREF results, the elution peak of PP-2 (124.0 degrees C, 91.7%) is 1.5 degrees C higher than the isotactic fraction from PP-4 (122.5 degrees C, 87.2%), and even 1.2 degrees C higher than PP-5 prepared from ID-3 with the characteristics of high stereoregularity. Moreover, the pentad methyl sequence mmmm of PP-2 (93.0%) from cat-2 is 0.5% higher than that of PP-4 from cat-4. XPS analysis revealed that the minute difference in binding energy of Ti, Mg, C and O atoms exist between the inorganic MgCl2 and the organic polymer based Z-N catalysts. The plausible interaction mechanism of active sites of Mg and Ti with the functional groups in the POP support and the added ID was proposed, which could be explained by their high stereoregularity and the broad molecular weight distribution of the POP-based Z-N catalysts.
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