Propylene-diene copolymer resin having excellent melt tension

Patent metadata

Field	Value
Publication number	US-10875951-B2
Application number	US-201716091658-A
Country	US
Kind code	B2
Filing date	Apr 6, 2017
Priority date	Apr 6, 2016
Publication date	Dec 29, 2020
Grant date	Dec 29, 2020

Abstract

Disclosed is a propylene-diene copolymer resin having excellent melt tension, with improved melt strength, high molecular weight and broad molecular weight distribution by using a specific metallocene catalyst system. The present invention provides a propylene-diene copolymer resin produced by polymerizing propylene and a diene compound of C4-C20 by using a metallocene catalyst system, wherein the propylene-diene copolymer resin has the melt index (2.16 kg load at 230° C.) of 0.1-100 g/10 min and the melt tension (advanced rheometric expansion system (ARES)) of 5-100 g.

First claim

The invention claimed is:

1. A propylene-diene copolymer resin produced by a method comprising the step of polymerizing propylene and a diene compound of C4-C20 by using a catalyst system,
wherein the catalyst system comprises: a metallocene compound represented by the following Chemical Formula 1; and at least one cocatalyst compound selected from the group consisting of a boron compound represented by the following Chemical Formulae 2 to 4 and an aluminum compound represented by the following Chemical Formulae 5 to 9, and
the propylene-diene copolymer resin has the melt index (2.16 kg load at 230° C.) of 0.1-100 g/10 min and the melt tension (advanced rheometric expansion system (ARES)) of 5-100 g:
B(R 11 ) 3   [Chemical Formula 2]

[R 12 ] + [B(R 11 ) 4 ] −   [Chemical Formula 3]

[(R 13 ) r ZH] + [B(R 11 ) 4 ] −   [Chemical Formula 4]

—[Al(R 14 )—O] s —  [Chemical Formula 5]

(R 14 ) 2 Al—[O(R 14 )] t —(R 14 ) 2   [Chemical Formula 6]

(R 15 ) u Al(E) 3-u   [Chemical Formula 7]

(R 16 ) 2 AlOR 17   [Chemical Formula 8]

R 16 Al(OR 17 ) 2   [Chemical Formula 9]

in Chemical Formula 1, M is a tetravalent or divalent group 4 transition metal of the periodic table, and m is 2 and n is 0 when M is a tetravalent transition metal of group 4 of the periodic table, and m is 0 and n is 1 when M is a divalent transition metal of group 4 of the periodic table; Cp is a cyclopentadienyl ring which may be η 5 -bonded to M and the cyclopentadienyl ring may be further substituted by at least one selected from the group consisting of (C1-C20) alkyl, (C3-C20) cycloalkyl, (C6-C20) aryl, tri(C1-C20) alkylsilyl, tri(C6-C20) arylsilyl, (C1-C20) alkyldi (C6-C20) arylsilyl, (C6-C20) aryldi (C1-C20) alkylsilyl and (C2-C20) alkenyl; D is SiR 3 R 4 or (C2-C20) alkenylene; R 3 and R 4 are each independently hydrogen, (C1-C20) alkyl, (C3-C20) cycloalkyl or (C6-C20) aryl, or R 3 and R 4 may be linked by (C4-C7) alkylene to form a ring; R 1 is (C1-C20) alkyl; Ar is (C6-C20) aryl; R 2 is hydrogen, (C1-C20) alkyl, (C3-C20) cycloalkyl or (C6-C20) aryl; the Ar and R 2 may be linked by (C1-C7) alkylene, (C2-C7) alkenylene or (C4-C7) alkane dienylene to form a fused ring; X 1 is halogen, (C1-C20) alkyl, (C1-C20) alkoxy, (C3-C20) cycloalkyl, (C6-C20) aryl, (C6-C20) aryloxy, —OSiR a R b R c , —SR d , —NR e R f , or —PR g R h ; R a to R h are each independently (C1-C20) alkyl, (C6-C20) aryl or (C3-C20) cycloalkyl; X 2 is a neutral, conjugated or nonconjugated (C4-C20) diene; the alkyl in R 1 , the aryl in Ar, the alkyl, cycloalkyl, and aryl in R 2 , R 3 , and R 4 may be each independently further substitute by at least one substituent selected from the group consisting of halogen, (C1-C20) alkyl, halo (C1-C20) alkyl, (C3-C20) cycloalkyl, (C6-C20) aryl, (C1-C20) alkoxy and (C6-C20) aryloxy;
in Chemical Formulae 2 to 4, B is a boron atom; R 11 is phenyl, and the phenyl may be further substituted by three to five substituents selected from a fluorine atom, (C1-C20) alkyl, (C1-C20) alkyl substituted by a fluorine atom, (C1-C20) alkoxy, and (C1-C20) alkoxy substituted by a fluorine atom; R 12 is a (C5-C7) aromatic radical or a (C1-C20) alkyl (C6-C20) aryl radical or a (C6-C20) aryl (C1-C20) alkyl radical; Z is a nitrogen or phosphorus atom; R 13 is a (C1-C20) alkyl radical or an anilinium radical substituted by two (C1-C10) alkyls together with a nitrogen atom; r is an integer of 2 or 3;
in Chemical Formulae 5 to 9, R 14 is (C1-C20) alkyl; s and t are each independently an integer of 5 to 20; R 15 and R 16 are each independently (C1-C20) alkyl; E is a hydrogen atom, a halogen atom or (C1-C20) alkyl; u is an integer of 1 to 3; R 17 is (C1-C20) alkyl or (C6-C20) aryl, and
the propylene-diene copolymer resin comprises two melting peaks at 140 to 154° C. and 129 to 135° C. respectively.

2. The propylene-diene copolymer resin of claim 1 ,
wherein in the step of polymerizing, the content of the diene compound is prepared in 0.001 to 3 mol % based on the propylene.

3. The propylene-diene copolymer resin of claim 1 ,
wherein the diene compound is at least one selected from the group consisting of linear or branched C4-C20 diene or C5-C20 cyclodiene.

4. The propylene-diene copolymer resin of claim 3 ,
wherein the diene compound is at least one selected from the group consisting of 1,3-butadiene, 1,4-pentadiene, 2-methyl-1,3-butadiene, 1,4-hexadiene, 1,5-hexadiene, 1,5-heptadiene, 1,6-heptadiene, 1,6-octadiene, 1,7-octadiene, 1,7-nonadiene, 1,8-nonadiene, 1,8-decadiene, 1,9-decadiene, 1,12-tetradecadiene, 1,13-tetradecadiene, 3-methyl-1,4-hexadiene, 3-methyl-1,5-hexadiene, 3-ethyl-1,4-hexadiene, 3-ethyl-1,5-hexadiene, 3,3-dimethyl-1,4-hexadiene, 3,3-dimentyl-1,5-hexadiene, cyclopentadiene, cyclohexadiene, cycloheptadiene, and cyclooctadiene.

5. The propylene-diene copolymer resin of claim 1 ,
wherein the propylene-diene copolymer resin has the gel content of 10% by weight or less.

Assignees

• Lotte Chemical Corp

Inventors

• Chae Byung Hun
• Woo Hyun Yul
• Lee Rai Ha
• Min Joon Keun
• Jung Sung Won
• Hong Youn Jin
• Shin Eun Hye

Classifications

• C08F10/06 Primary

  Propene · CPC title

• C08F4/65912

  in combination with an organoaluminium compound · CPC title

• C08F2420/01

  Cp or analog bridged to a non-Cp X neutral donor · CPC title

• C08F2800/10

  as molar percentages · CPC title

• C08F210/06

  Propene · CPC title