Amide ester internal electron donor and process
View Patent ↗Disclosed is a process for producing a procatalyst composition having an amide ester internal electron donor. The process includes pre-halogenating a procatalyst precursor before reaction with the amide ester and forming the procatalyst composition. Ziegler-Natta catalyst compositions containing the present procatalyst composition exhibit improved catalyst activity and/or improved catalyst selectivity and produce propylene-based olefins with broad molecular weight distribution.
1. A process comprising:
pre-halogenating a procatalyst precursor with a halogenating agent;
adding an amide ester to the halogenated procatalyst precursor in a reaction mixture, the amide ester having the structure (II);
wherein R 1 -R 6 , R 11 -R 13 , and R 21 -R 23 are the same or different, each of R 1 -R 6 , R 11 , R 13 R 21 , and R 23 is selected from a group consisting of hydrogen, a halogen, a substituted hydrocarbyl group having 1-20 carbon atoms, an unsubstituted hydrocarbyl group having 1-20 atoms, and combinations thereof and R 12 and R 22 , each is a halogen; and
forming a procatalyst composition comprising a magnesium moiety, a titanium moiety, and an internal electron donor comprising the amide ester.
2. The process of claim 1 comprising pre-halogenating a procatalyst precursor selected from a group consisting of a magnesium moiety compound, a magnesium mixed metal compound, a benzoate-containing magnesium chloride compound, and combinations thereof
3. The process of claim 1 comprising reacting the amide ester with the prehalogenated procatalyst precursor in the presence of titanium tetrachloride wherein the prehalogenated procatalyst precursor is a benzoate containing magnesium chloride compound.
4. The process of claim 1 comprising introducing, to the reaction mixture, an electron donor component; and
forming a procatalyst composition comprising a mixed internal electron donor comprising the amide ester and the electron donor component.
5. The process of claim 1 comprising adding an amide ester to the halogenated procatalyst precursor in a reaction mixture, the amide ester having the structure (II) wherein R 1 and R 2 each is an unsubstituted hydrocarbyl group having 1-6 carbon atoms.