Propylene-based terpolymer composition for pipes

Patent metadata

Field	Value
Publication number	US-2021214540-A1
Application number	US-201917263338-A
Country	US
Kind code	A1
Filing date	Jul 22, 2019
Priority date	Jul 27, 2018
Publication date	Jul 15, 2021
Grant date	—

Abstract

The invention relates to a polypropylene composition comprising a terpolymer composition comprising (A) a first terpolymer fraction containing propylene, ethylene and 1-hexene, wherein the first terpolymer fraction has a melt flow rate of 0.005 to 0.20 dg/min determined by ISO 1133-1:2011 (230° C., 2.16 kg) and (B) a second terpolymer fraction containing propylene, ethylene and 1-hexene, wherein the second terpolymer fraction has a melt flow rate of 0.30 to 70 dg/min determined by ISO 1133-1:2011 (230° C., 2.16 kg), wherein the first terpolymer fraction is prepared using a first set of reaction conditions, the second terpolymer fraction is prepared using a second set of reaction conditions and the first and second set of reaction conditions are different, wherein the polypropylene composition (i) has a melt flow rate of 0.10 to 0.70 dg/min determined by ISO 1133-1:2011 (230° C., 2.16 kg), (ii) has a content of ethylene derived units in the range from 1.6 to 3.0 wt %; (iii) has a content of 1-hexene derived units in the range from 1.7 to 4.0 wt %; and (iv) has a ratio of the content of ethylene derived units to the content of 1-hexene derived units in the composition of at least 0.70.

First claim

1 . A polypropylene composition comprising a terpolymer composition comprising (A) a first terpolymer fraction containing propylene, ethylene and 1-hexene, wherein the first terpolymer fraction has a melt flow rate of 0.030 to 1.0 dg/min determined by ISO 1133-1:2011 (230° C., 5 kg) and (B) a second terpolymer fraction containing propylene, ethylene and 1-hexene, wherein the second terpolymer fraction has a melt flow rate of 0.30 to 70 dg/min determined by ISO 1133-1:2011 (230° C., 2.16 kg),
wherein the first terpolymer fraction is prepared using a first set of reaction conditions, the second terpolymer fraction is prepared using a second set of reaction conditions and the first and second set of reaction conditions are different, wherein the polypropylene composition
(i) has a melt flow rate of 0.10 to 0.70 dg/min determined by ISO 1133-1:2011 (230° C., 2.16 kg);
(ii) has a content of ethylene derived units in the range from 1.6 to 3.5 wt %;
(iii) has a content of 1-hexene derived units in the range from 1.7 to 4.0 wt %; and
(iv) has a ratio of the content of ethylene derived units to the content of 1-hexene derived units of at least 0.70.

2 . The polypropylene composition according to claim 1 , wherein the melt flow rate of the polypropylene composition determined by ISO 1133-1:2011 (230° C., 2.16 kg) is in the range from 0.10 to 0.50 dg/min.

3 . The polypropylene composition according to claim 1 , wherein the content of ethylene derived units in the polypropylene composition is 1.7 to 3.0 wt %.

4 . The polypropylene composition according to claim 1 , wherein the content of 1-hexene derived units in the polypropylene composition is 1.8 to 3.0 wt %.

5 . The polypropylene composition according to claim 1 , wherein the ratio of the content of ethylene derived units to the content of 1-hexene derived units in the polypropylene composition is at least 0.80.

6 . The polypropylene composition according to claim 1 , wherein the content of ethylene derived units in the polypropylene composition in wt % is larger than the content of 1-hexene derived units in the polypropylene composition in wt %-0.20 wt %.

7 . The polypropylene composition according to claim 1 , wherein the weight ratio of the first terpolymer fraction to the second terpolymer fraction in the polypropylene composition is 0.20 to 5.0.

8 . The polypropylene composition according to claim 1 , wherein the ratio of weight average molecular weight to numeric average molecular weight (Mw/Mn) of the composition is in the range from 7.0 to 25.0, wherein the Mw and Mn are measured according to ASTM D6474-12, and/or wherein the polypropylene composition has a polydispersity index (PI) of 5.0 to 15.0.

9 . The polypropylene composition according to claim 1 , wherein the composition according to the invention has <Gp>/Y of at least 7.0, wherein <Gp> is strain hardening modulus and Y is yield stress and <Gp>/Y is determined by:
a) providing a specimen of the composition by compression molding a sheet from the composition according to ISO 1873-2 to a thickness of 0.3 mm±0.025 mm and punching a specimen having a geometry of the test specimen described in ISO/DIS 18488 from the sheet, wherein the sheet is annealed after the compression molding and before the punching at a temperature of 100° C. for 1 hour and cooled down to room temperature,
b) elongating the specimen at a constant traverse speed of 20 mm/min at 100° C.,
c) measuring the load sustained by the specimen during the elongation to obtain a stress-strain curve and measuring the yield stress Y,
d) calculating true stress-true strain curve from the stress strain curve obtained by step c) and calculating the tensile strain hardening modulus <Gp> from the true stress-strain curve, according to the method as described in ISO/DIS 18488 and
e) calculating a quotient of the tensile strain hardening modulus <Gp> divided by the yield stress Y.

10 . The polypropylene composition according to claim 1 , wherein the polypropylene composition comprises additives and the sum of the amounts of the first terpolymer, the second terpolymer and the additives is 100 wt % of the polypropylene composition.

11 . A process for the preparation of the polypropylene composition according to claim 1 , comprising preparing the terpolymer composition by a process comprising the steps of
preparing the first terpolymer fraction by polymerizing propylene, ethylene and 1-hexene in the presence of a Ziegler-Natta catalyst system using a first set of reaction conditions, preparing the second terpolymer fraction by polymerizing propylene, ethylene and 1-hexene in the presence of a Ziegler-Natta catalyst system using a second set of reaction conditions, wherein the first set of reaction conditions and the second set of reaction conditions differ in one or more conditions chosen from the group of pressure, temperature, propylene concentration, ethylene concentration, 1-hexene concentration and hydrogen concentration.

12 . The process according to claim 11 , wherein the first terpolymer fraction and the second terpolymer fraction are prepared in a single reactor to obtain the terpolymer composition.

13 . The process according to claim 11 , wherein the Ziegler-Natta catalyst system comprises a procatalyst, a co-catalyst and optionally an external electron donor, wherein the procatalyst id obtained by a process comprising the steps of
Step A) providing or preparing a compound R4zMgX42-z wherein R4 is independently selected from linear, branched or cyclic hydrocarbyl group independently selected from alkyl, alkenyl, aryl, aralkyl, or alkylaryl groups, and one or more combinations thereof; wherein said hydrocarbyl group may be substituted or unsubstituted, may contain one or more heteroatoms; X4 is independently selected from the group consisting of fluoride (F—), chloride (CI—), bromide (Br—) or iodide (I), preferably chloride; z is in a range of larger than 0 and smaller than 2, being 0<z<2; Step B) contacting the compound R4zMgX42-z with a silane compound Si(OR5)4-n(R6)n to give a first intermediate reaction product, being a solid Mg(OR1)xX12-x wherein R1, R5 and R6 are each independently selected from linear, branched or cyclic hydrocarbyl group independently selected from alkyl, alkenyl, aryl, aralkyl, alkoxycarbonyl or alkylaryl groups, and one or more combinations thereof; wherein said hydrocarbyl group may be substituted or unsubstituted, may contain one or more heteroatoms; X1 is independently selected from the group consisting of fluoride (F—), chloride (CI—), bromide (Br—) or iodide (I—); n is in range of 0 to 4; z is in a range of larger than 0 and smaller than 2, being 0<z<2; x is in a range of larger than 0 and smaller than 2, being 0<x<2; Step C) activating said solid support, comprising two sub steps: Step C1) a first activation step by contacting the first intermediate reaction product obtained in step B) with at least one first activating compound being a metal alkoxide compound of formula M1(OR2)v-w(OR3)w or M2(OR2)v-w(R3)w; wherein: M1 is a metal selected from the group consisting of Ti, Zr, Hf, Al or Si; M2 is a metal being Si; v is the valency of M1 or M2 and w is smaller than v; R2 and R3 are each a linear, branched or cyclic hydrocarbyl group independently selected from alkyl, alkenyl, aryl, aralkyl, alkoxycarbonyl or alkylaryl groups, and one or more combinations thereof; wherein said hydrocarbyl group may be substituted or unsubstituted, may contain one or more heteroatoms; and a second activating compound being an activating electron donor; and Step C2) a second activation step by contacting the activated solid support obtained in step C1) w

Assignees

• Sabic Global Technologies Bv

Inventors

• Steenbakkers-Menting Henrica Norberta Alberta Maria
• Ndoro Tinashe Victor Mandishonha
• Seegers Desiree Marie Louise
• Delsman Erik
• Gerlofsma Raymond
• Kiggen Tim
• Zuideveld Martin Alexander
• Moman Akhlaq
• Voets Patrick Elisabeth Luc

Classifications

• C08L23/12 Primary

  Polypropene · CPC title

• C08L2203/18

  used for pipes · CPC title

• C08L23/142 Primary

  at least partially crystalline copolymers of propene with other olefins · CPC title

• C08L2205/025

  containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure · CPC title

• G01N33/442

  Resins; Plastics · CPC title