Long chain branched polypropylene

Patent metadata

Field	Value
Publication number	US-10072107-B2
Application number	US-201415102073-A
Country	US
Kind code	B2
Filing date	Dec 5, 2014
Priority date	Dec 6, 2013
Publication date	Sep 11, 2018
Grant date	Sep 11, 2018

Abstract

A process for preparing a long chain branched polypropylene in presence of two metallocene-based active catalyst systems is provided. The polypropylene obtained therefrom has new molecular architecture and improved elasticity properties. The polypropylene is further characterized by new signals in its 13C NMR spectrum.

First claim

The invention claimed is:

1. A process for the preparation of polypropylene having long chain branchings comprising the steps of:
(a) providing in a reactor a first active catalyst system comprising an activating agent having an alkylating and/or ionizing action and a first precatalyst of formula (I)

wherein M is a group IV transition metal;
wherein Q 1 and Q 2 are identical or different and are independently selected from the group consisting of amido, halogen, C 1 -C 10 alkyl group, C 6 -C 20 aryl group, an anionic ligand or a neutral ligand capable of coordination by a lone pair of electrons;
wherein R″ is of formula —[Z(R 1 )(R 2 )] n —
wherein n is an integer between 1 and 5;
wherein Z is a carbon or silicon;
wherein R 1 and R 2 are identical or different and are independently selected from the group consisting of hydrogen, C 1 -C 30 alkyl groups optionally substituted by one or more substituents, C 1 -C 30 alkenyl groups optionally substituted by one or more substituents, C 6 -C 40 aryl groups optionally substituted by one or more substituents, or R 1 and R 2 together with the atom Z to which they are attached form a three- to thirty-membered ring optionally substituted by one or more substituents;
wherein R 3 to R 10 are identical or different and are independently selected from the group consisting of hydrogen, C 1 -C 30 alkyl groups optionally substituted by one or more substituents, C 6 -C 40 aryl groups optionally substituted by one or more substituents, or two of the substituents R 3 to R 6 or R 7 to R 10 attached to a carbon atom positioned vicinal to each other respectively, form with the carbon atom to which they are attached a cycloalkenyl or aryl group optionally substituted by one or more substituents;
with the proviso that said first precatalyst is not [R(2-R′ 3 Si-Ind) 2 ]MQ 2 wherein R′ is alkyl having from 1 to 6 carbon atoms and R is a C- or Si-bridge between the two indenyl moieties;
(b) injecting propylene, either before or after or simultaneously with step (a), to produce polypropylene macromers;
(c) contacting a second active catalyst system with the polypropylene macromers formed in (b) without isolating the propylene macromers formed in (b), wherein the second active catalyst system comprises a second precatalyst and an activating agent having an alkylating and/or ionizing action, said second precatalyst being different from said first precatalyst and being of formula (I) as defined above without the proviso,

wherein a weight ratio between the first precatalyst and the second precatalyst is from 1/2 to 100/1;
(d) wherein polymerization conditions are maintained throughout (a)-(c);
(e) retrieving a long chain branched polypropylene, wherein the long chain branched polypropylene has a total content of long chain branchings of higher than 5 per 10,000 C and the long chain branch has a number average (Mn) of at least 6,000 g/mol.

2. The process according to claim 1 , wherein the polypropylene macromers have at least a molecular weight Mn greater than 6,000 g mol −1 or have at least 420 carbon atoms.

3. The process according to claim 1 , wherein (a) and (c) are carried out simultaneously by contacting the first and second precatalysts in the reactor together with the propylene.

4. The process according to claim 1 , wherein said second active catalyst system is able to produce polypropylene incorporating said polypropylene macromers.

5. The process according to claim 1 , wherein said first and second precatalysts are of formula (IIa), (IIb), or (IIc)

wherein M is a group IV transition metal;
wherein Q 1 and Q 2 are identical or different and are independently selected from the group consisting of amido, halogen, C 1 -C 10 alkyl group, C 6 -C 20 aryl group, an anionic ligand or a neutral ligand capable of coordination by a lone pair of electrons;
wherein R″ is of formula —[Z(R 1 )(R 2 )] n —
wherein n is an integer between 1 and 5;
wherein Z is a carbon or silicon;
wherein R 1 and R 2 are identical or different and are independently selected from the group consisting of hydrogen, C 1 -C 30 alkyl groups optionally substituted by one or more substituents, C 1 -C 30 alkenyl groups optionally substituted by one or more substituents, C 6 -C 40 aryl groups optionally substituted by one or more substituents, or R 1 and R 2 together with the atom Z to which they are attached form a three- to thirty-membered ring optionally substituted by one or more substituents;
wherein R 3 to R 8 , R 13 to R 28 and R 30 to R 33 are identical or different and are independently selected from the group consisting of hydrogen, C 1 -C 30 alkyl groups optionally substituted by one or more substituents, C 1 -C 30 alkenyl groups optionally substituted by one or more substituents, C 6 -C 40 aryl groups optionally substituted by one or more substituents, or two of the substituents R 3 to R 8 , R 13 to R 28 and R 30 to R 33 attached to a carbon atom positioned vicinal to each other respectively, form with the carbon atom to which they are attached a cycloalkenyl or aryl group optionally substituted by one or more substituents;
with the proviso that said first precatalyst is not [R(2-R′ 3 Si-Ind) 2 ]MQ 2 wherein R′ is alkyl having from 1 to 6 carbon atoms and R is a C- or Si-bridge between the two indenyl moieties.

6. The process according to claim 1 , characterized in that said first precatalyst is of formula (III)

wherein R 1 is hydrogen or a hydrocarbyl group having from 1 to 20 carbon atoms,
wherein R 2 , R 3 , R 5 , are each, independently from one another, hydrogen, C 1 -C 30 alkyl groups optionally substituted by one or more substituents, C 1 -C 30 alkenyl groups optionally substituted by one or more substituents, C 6 -C 40 aryl groups optionally substituted by one or more substituents,
wherein R 30 , R 31 , R 32 , R 33 are each, independently from one another, hydrogen, C 1 -C 30 alkyl groups optionally substituted by one or more substituents, C 6 -C 40 aryl groups optionally substituted by one or more substituents, or R 30 and R 31 or R 32 and R 33 form with the carbon atom to which they are attached a cycloalkenyl or aryl group optionally substituted by one or more substituents.

7. The process according to claim 1 , wherein said second precatalyst is of formula (IIa) or (IIb)

wherein R 3 to R 8 , R 13 to R 20 and R 30 to R 33 are identical or different and are independently selected from the group consisting of hydrogen, C 1 -C 30 alkyl groups optionally substituted by one or more substituents, C 6 -C 40 aryl groups optionally substituted by one or more substituents, or two of the substituents R 3 to R 8 , R 13 to R 20 and R 30 to R 33 attached to a carbon atom positioned vicinal to each other respectively, form with the carbon atom to which they are attached a cycloalkenyl or aryl group optionally substituted by one or more substituents.

8. The process according to claim 1 , wherein the weight ratio between the first precatalyst and the second precatalyst is 1/1 to 50/1.

9. The process according to claim 1 , wherein step (b) is performed at a temperature higher than

Assignees

• Total Res & Technology Feluy
• Centre Nat Rech Scient

Inventors

• Bader Manuela
• Carpentier Jean-François
• Kirillov Evgueni
• Lhost Olivier
• Lamotte Christian
• Den Dauw Katty

Classifications

• C08F4/65927

  two cyclopentadienyl rings being mutually bridged · CPC title

• C08F4/65904

  in combination with another component of C08F4/64 · CPC title

• C08F2/001

  Multistage polymerisation processes characterised by a change in reactor conditions without deactivating the intermediate polymer (C08F295/00, C08F297/00 take precedence) · CPC title

• C08F4/65912

  in combination with an organoaluminium compound · CPC title

• C08F110/06 Primary

  Propene · CPC title