A fourth generation multiple site Ziegler-Natta catalyst was used to synthesize ethylene and propylene homo-and copolymers in the presence of hydrogen. This type of catalysts produce polymers with broader molecular weight distribution (MWD), chemical composition distribution (CCD) and stereoregularity than other coordination polymerization catalysts since it has more than one active site. The ratio of propylene/ethylene was varied to study its effect on polymer microstructure. In addition, by having two different electron donors, namely diisopropyldimethoxysilane (P) and dicyclopentyldimethoxysilane (D), the molecular weight distribution (MWD) and stereospecificity of the synthesized polymers were examined. The polymer samples were characterized using 13C-NMR and high-temperature gel permeation chromatography (GPC). Using the 13C-NMR data, the triad distribution for the copolymers and also the isotactic triad distribution for homo-polymers were calculated. The effects of electron donors on different feed ratios of ethylene and propylene in the synthesis were investigated. Co-polymer produced with D-donors showed higher isospecificity and also higher content of ethylene in the final polymer. In contrast, polymers produced using with P-donor showed lower polydispersity indices (PDI), and had higher contents of propylene in final polymer. In addition, the “Deconvolution method” was applied to GPC data in order to determine the number of sites on the Ziegler-Natta catalyst; which showed that 4 active site types were adequate to explain the molecular weight distributions.
| Identifer | oai:union.ndltd.org:UPSALLA1/oai:DiVA.org:kth-147523 |
| Date | January 2012 |
| Creators | Shafagh Dehghani, Seyedeh |
| Publisher | KTH, Skolan för kemivetenskap (CHE) |
| Source Sets | DiVA Archive at Upsalla University |
| Language | English |
| Detected Language | English |
| Type | Student thesis, info:eu-repo/semantics/bachelorThesis, text |
| Format | application/pdf |
| Rights | info:eu-repo/semantics/openAccess |
Page generated in 0.0023 seconds