Heterogeneous Ziegler-Natta Catalyst System And A Process For Olefin Polymerization Using The Same
US-2015344593-A1 · Dec 3, 2015 · US
US10094399B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10094399-B2 |
| Application number | US-201615233480-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 10, 2016 |
| Priority date | Nov 30, 2015 |
| Publication date | Oct 9, 2018 |
| Grant date | Oct 9, 2018 |
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The present invention relates to a process for preparing ultra-high molecular weight polyalphaolefin. The process consists of polymerizing alphaolefin monomers using the catalyst system consisting of supported Ziegler-Natta catalyst without internal donor in presence of co-catalyst based on alkyl aluminums. The resulting ultra-high molecular weight polyalphaolefins having intrinsic viscosity ≥10 dL/g are used as drag reducing polymers for increasing throughput in the pipelines by reducing frictional resistance in turbulent flow.
Opening claim text (preview).
We claim: 1. A process for preparing polyalphaolefin having ultra-high molecular weight, the process comprising: (i) contacting a mixture of supported Ziegler-Natta catalyst without internal donor and a co-catalyst with an alphaolefin monomer to obtain a polymerization mixture: (ii) keeping the polymerization mixture of step (i) at temperature in the range of 15° C. to 30° C. for at least 24 hours; and (iii) keeping the polymerization mixture of step (ii) at temperature in the range of 20° C. to 35° C. for at least 14 days to achieve conversion of >90%. 2. The process as claimed in claim 1 , wherein the polymerization is conducted in bulk under inert and oxygen free conditions. 3. The process as claimed in claim 1 , wherein the supported Ziegler-Natta catalyst is combination of magnesium based precursor and transition metal compound without internal donor. 4. The process as claimed in claim 1 , wherein the co-catalyst is organoaluminum having at least four carbon atoms (C4). 5. The process as claimed in claim 1 , wherein the mole ratio of the co-catalyst and the Ziegler-Natta catalyst is in the range of 1 to 250, preferably in the range of 1.5 to 150, more preferably in the range of 1.5 to 100. 6. The process as claimed in claim 1 , wherein the alpha olefin monomer selected from the group comprising of C4 and above alpha olefin monomers. 7. The process as claimed in claim 1 , wherein the process optionally comprises external donor selected from alkoxysilane. 8. The process as claimed in claim 1 , wherein polyalphaolefin having ultrahigh molecular weight have intrinsic viscosity ≥10 dL/g and are used as drag reducing polymers. 9. The process as claimed in claim 1 , wherein the supported Ziegler-Natta catalyst without internal donor is prepared by contacting magnesium based precursor with a transition metal compound in presence of a solvent. 10. The process as claimed in claim 9 , wherein the wherein the magnesium based precursor is solid in nature and is prepared by first contacting the magnesium with organohalide in presence of solvating agent as the first step and then followed by addition of alcohol. 11. The process as claimed in claim 9 , wherein the magnesium based precursor is liquid in nature and is prepared by contacting magnesium source with organohalide and alcohol in presence of a solvent in a single step. 12. The process as claimed in claim 9 , wherein the procedure of contacting the transition metal component is essentially repeated three times for having a catalyst that provides polyalphaolefin having Intrinsic Viscosity ≥10 dL/g. 13. The process as claimed in claim 1 , wherein the supported Ziegler-Natta catalyst without internal donor comprises transition metal from 3.0 wt % to 8.0 wt% and magnesium is from 15 wt % to 25 wt %.
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