JP2009299045A5 - - Google Patents

Download PDF

Info

Publication number
JP2009299045A5
JP2009299045A5 JP2009115464A JP2009115464A JP2009299045A5 JP 2009299045 A5 JP2009299045 A5 JP 2009299045A5 JP 2009115464 A JP2009115464 A JP 2009115464A JP 2009115464 A JP2009115464 A JP 2009115464A JP 2009299045 A5 JP2009299045 A5 JP 2009299045A5
Authority
JP
Japan
Prior art keywords
terminal
ratio
characteristic
average molecular
vinyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2009115464A
Other languages
Japanese (ja)
Other versions
JP5286154B2 (en
JP2009299045A (en
Filing date
Publication date
Application filed filed Critical
Priority to JP2009115464A priority Critical patent/JP5286154B2/en
Priority claimed from JP2009115464A external-priority patent/JP5286154B2/en
Publication of JP2009299045A publication Critical patent/JP2009299045A/en
Publication of JP2009299045A5 publication Critical patent/JP2009299045A5/ja
Application granted granted Critical
Publication of JP5286154B2 publication Critical patent/JP5286154B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Description

本発明者等は、上記課題を解決するため、鋭意検討した結果、特定の平均分子量(Mn)、Q値、末端ビニル率、末端ビニリデン率、昇温溶出分別における40℃以下の温度で溶出する成分量、13C−NMR分析によって得られるプロピレン単位3連鎖のmm分率を有する、ポリプロピレン単独重合体が上記の課題を解決できることを見出し、本発明に到達した。 As a result of intensive studies to solve the above-mentioned problems, the present inventors have eluted at a specific number average molecular weight (Mn), Q value, terminal vinyl ratio, terminal vinylidene ratio, and a temperature of 40 ° C. or less in temperature rising elution fractionation The present inventors have found that a polypropylene homopolymer having an amount of components to be obtained and a mm fraction of three chains of propylene units obtained by 13 C-NMR analysis can solve the above-mentioned problems.

すなわち、本発明の第1の発明によれば、下記(1)〜(5)の特性を有することを特徴とするプロピレン系重合体が提供される。
特性(1):GPCによって得られる平均分子量(Mn)が5万より大きく13万未満。
特性(2):GPCによって得られる重量平均分子量(Mw)と数平均分子量(Mn)との比(Q値)が2.0以上4.0以下。
特性(3):全ポリマー鎖のうち末端にビニル基を持つ鎖の割合(末端ビニル率)と、末端にビニリデン基を持つ鎖の割合(末端ビニリデン率)が、それぞれ下式を満たす。
(末端ビニル率)=Mn/21000×[Vi]≧0.7
(末端ビニリデン率)=Mn/21000×[Vd]<0.1
(ただし、Mnは、GPCによりもとめた数平均分子量、[Vi]は、13C−NMRより算出する1000C当りの末端ビニル基の数、[Vd]は、13C−NMRより算出する1000C当りの末端ビニリデン基の数である。)
特性(4):オルトジクロロベンゼンを溶媒として使用した昇温溶出分別(TREF)の測定において、40℃以下の温度で溶出する成分が3重量%以下。
特性(5):13C−NMR分析によって得られるプロピレン単位3連鎖のmm分率が95%以上。
That is, according to the first invention of the present invention, there is provided a propylene-based polymer having the following characteristics (1) to (5).
Characteristic (1): The number average molecular weight (Mn) obtained by GPC is more than 50,000 and less than 130,000.
Characteristic (2): The ratio (Q value) between the weight average molecular weight (Mw) and the number average molecular weight (Mn) obtained by GPC is 2.0 or more and 4.0 or less.
Characteristic (3): The ratio of the chain having a vinyl group at the terminal (terminal vinyl ratio) and the ratio of the chain having a vinylidene group at the terminal (terminal vinylidene ratio) among all polymer chains satisfy the following formulas.
(Terminal vinyl ratio) = Mn / 21000 × [Vi] ≧ 0.7
(Vinyl terminal ratio) = Mn / 21000 × [Vd] <0.1
(However, Mn is the number average molecular weight determined by GPC, [Vi] is the number of terminal vinyl groups per 1000 C calculated from 13 C-NMR, and [Vd] is the number per 1000 C calculated from 13 C-NMR. (The number of terminal vinylidene groups.)
Characteristic (4): In the temperature rising elution fractionation (TREF) measurement using orthodichlorobenzene as a solvent, the component eluted at a temperature of 40 ° C. or less is 3% by weight or less.
Characteristic (5): mm fraction of propylene unit 3 chain obtained by 13 C-NMR analysis is 95% or more.

Claims (1)

下記(1)〜(5)の特性を有することを特徴とするプロピレン系重合体。
特性(1):GPCによって得られる平均分子量(Mn)が5万より大きく13万未満。
特性(2):GPCによって得られる重量平均分子量(Mw)と数平均分子量(Mn)との比(Q値)が2.0以上4.0以下。
特性(3):全ポリマー鎖のうち末端にビニル基を持つ鎖の割合(末端ビニル率)と、末端にビニリデン基を持つ鎖の割合(末端ビニリデン率)が、それぞれ下式を満たす。
(末端ビニル率)=Mn/21000×[Vi]≧0.7
(末端ビニリデン率)=Mn/21000×[Vd]<0.1
(ただし、Mnは、GPCによりもとめた数平均分子量、[Vi]は、13C−NMRより算出する1000C当りの末端ビニル基の数、[Vd]は、13C−NMRより算出する1000C当りの末端ビニリデン基の数である。)
特性(4):オルトジクロロベンゼンを溶媒として使用した昇温溶出分別(TREF)の測定において、40℃以下の温度で溶出する成分が3重量%以下。
特性(5):13C−NMR分析によって得られるプロピレン単位3連鎖のmm分率が95%以上。
A propylene-based polymer having the following properties (1) to (5):
Characteristic (1): The number average molecular weight (Mn) obtained by GPC is more than 50,000 and less than 130,000.
Characteristic (2): The ratio (Q value) between the weight average molecular weight (Mw) and the number average molecular weight (Mn) obtained by GPC is 2.0 or more and 4.0 or less.
Characteristic (3): The ratio of the chain having a vinyl group at the terminal (terminal vinyl ratio) and the ratio of the chain having a vinylidene group at the terminal (terminal vinylidene ratio) among all polymer chains satisfy the following formulas.
(Terminal vinyl ratio) = Mn / 21000 × [Vi] ≧ 0.7
(Vinyl terminal ratio) = Mn / 21000 × [Vd] <0.1
(However, Mn is the number average molecular weight determined by GPC, [Vi] is the number of terminal vinyl groups per 1000 C calculated from 13 C-NMR, and [Vd] is the number per 1000 C calculated from 13 C-NMR. (The number of terminal vinylidene groups.)
Characteristic (4): In the temperature rising elution fractionation (TREF) measurement using orthodichlorobenzene as a solvent, the component eluted at a temperature of 40 ° C. or less is 3% by weight or less.
Characteristic (5): mm fraction of propylene unit 3 chain obtained by 13 C-NMR analysis is 95% or more.
JP2009115464A 2008-05-13 2009-05-12 Propylene polymer Active JP5286154B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2009115464A JP5286154B2 (en) 2008-05-13 2009-05-12 Propylene polymer

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2008126462 2008-05-13
JP2008126462 2008-05-13
JP2009115464A JP5286154B2 (en) 2008-05-13 2009-05-12 Propylene polymer

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2013040305A Division JP5555785B2 (en) 2008-05-13 2013-03-01 Propylene polymer

Publications (3)

Publication Number Publication Date
JP2009299045A JP2009299045A (en) 2009-12-24
JP2009299045A5 true JP2009299045A5 (en) 2010-02-12
JP5286154B2 JP5286154B2 (en) 2013-09-11

Family

ID=41546258

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2009115464A Active JP5286154B2 (en) 2008-05-13 2009-05-12 Propylene polymer
JP2013040305A Active JP5555785B2 (en) 2008-05-13 2013-03-01 Propylene polymer

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2013040305A Active JP5555785B2 (en) 2008-05-13 2013-03-01 Propylene polymer

Country Status (1)

Country Link
JP (2) JP5286154B2 (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8372930B2 (en) 2008-06-20 2013-02-12 Exxonmobil Chemical Patents Inc. High vinyl terminated propylene based oligomers
US8283428B2 (en) 2008-06-20 2012-10-09 Exxonmobil Chemical Patents Inc. Polymacromonomer and process for production thereof
US8283419B2 (en) 2008-06-20 2012-10-09 Exxonmobil Chemical Patents Inc. Olefin functionalization by metathesis reaction
US8399725B2 (en) 2008-06-20 2013-03-19 Exxonmobil Chemical Patents Inc. Functionalized high vinyl terminated propylene based oligomers
US8802797B2 (en) 2008-06-20 2014-08-12 Exxonmobil Chemical Patents Inc. Vinyl-terminated macromonomer oligomerization
WO2012134715A2 (en) * 2011-03-25 2012-10-04 Exxonmobil Chemical Patents Inc. Branched vinyl terminated polymers and methods for production thereof
CN103890023B (en) 2011-10-24 2016-11-16 三菱化学株式会社 Composition for thermoplastic elastomer and manufacture method thereof
JP2014189776A (en) * 2013-03-28 2014-10-06 Mitsubishi Chemicals Corp Modified propylenic polymer composition
JP2014189775A (en) * 2013-03-28 2014-10-06 Mitsubishi Chemicals Corp Modified propylenic polymer composition
EP3848401A1 (en) * 2013-07-17 2021-07-14 ExxonMobil Chemical Patents Inc. Isotactic propylene polymers
WO2015166665A2 (en) 2015-08-24 2015-11-05 Sumitomo Chemical Company, Limited Injection-molded article for packaging material, injection-molded article for automotive part, industrial film, and food packaging film
WO2015166666A2 (en) 2015-08-24 2015-11-05 Sumitomo Chemical Company, Limited Injection-molded article for packaging material, injection-molded article for automotive part, industrial film, and food packaging film
JP6866813B2 (en) * 2016-11-02 2021-04-28 日本ポリプロ株式会社 Propylene-comonomer copolymer
JP6891584B2 (en) * 2017-03-27 2021-06-18 日本ポリプロ株式会社 Method for producing propylene polymer
JP7027988B2 (en) 2017-04-27 2022-03-02 住友化学株式会社 Propylene polymer composition
WO2020009090A1 (en) 2018-07-05 2020-01-09 住友化学株式会社 Propylene polymer composition
CN113574105B (en) * 2019-03-19 2023-04-25 三井化学株式会社 Propylene resin composition, molded article, and propylene polymer
KR102524952B1 (en) * 2019-06-13 2023-04-24 주식회사 엘지화학 Novel transition metal compound and method for preparing polypropylene with the same
JP7024842B2 (en) * 2020-10-16 2022-02-24 日本ポリプロ株式会社 Propene homopolymer

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3186218B2 (en) * 1992-05-20 2001-07-11 出光興産株式会社 Terminal vinyl ethylene-propylene copolymer and method for producing the same
US6117962A (en) * 1997-12-10 2000-09-12 Exxon Chemical Patents Inc. Vinyl-containing stereospecific polypropylene macromers
JPH11349634A (en) * 1998-06-05 1999-12-21 Mitsubishi Chemical Corp Propylene polymer
EP1209173A4 (en) * 1999-07-26 2003-04-16 Idemitsu Petrochemical Co Branched olefinic macromonomer, olefin graft copolymer, and olefin resin composition
JP2001163924A (en) * 1999-12-03 2001-06-19 Japan Polychem Corp Branched propylene polymer and manufacturing method thereof
JP2002194016A (en) * 2000-05-23 2002-07-10 Chisso Corp Metallocene compound, catalyst for olefin polymerization containing the same, and method for producing olefin polymer using the catalyst
JP4171880B2 (en) * 2001-08-06 2008-10-29 チッソ株式会社 Metallocene compound, process for producing olefin polymer using catalyst containing the same, and olefin polymer produced by the process
JP2004124044A (en) * 2002-08-02 2004-04-22 Chisso Corp Method for producing olefin polymer
JP4834965B2 (en) * 2004-05-26 2011-12-14 三菱化学株式会社 Novel transition metal compound and method for producing propylene polymer using the transition metal compound
JP5028010B2 (en) * 2005-12-08 2012-09-19 日本ポリプロ株式会社 Propylene homopolymer and process for producing the same
JP4524275B2 (en) * 2006-09-01 2010-08-11 日本ポリプロ株式会社 A vinyl group- and polar group-containing propylene copolymer and a method for producing a polymer using the same.
JPWO2008047860A1 (en) * 2006-10-20 2010-02-25 出光興産株式会社 High purity terminally unsaturated olefin polymer and process for producing the same
JP4637157B2 (en) * 2006-11-17 2011-02-23 日本ポリプロ株式会社 Propylene polymer and process for producing the same

Similar Documents

Publication Publication Date Title
JP2009299045A5 (en)
JP2014501323A5 (en)
JP2008525548A5 (en)
BR112012030036A2 (en) electronic device module comprising low unsaturation polyolefin copolymer and optional vinyl silane
JP2015523430A5 (en)
MX2012001581A (en) Improved polypropylene for use in bopp applications.
Jiang et al. Cellulose graft copolymers toward strong thermoplastic elastomers via RAFT polymerization
JP2012031414A5 (en)
JP2017527668A5 (en)
JP2018506619A5 (en)
JP2014169462A5 (en)
JP2013523900A5 (en)
EA201170485A1 (en) PROPYLENE POLYMERS FOR LABORATORY / MEDICAL EQUIPMENT
RU2013144577A (en) STYROL-BUTADIENE RUBBER WITH HIGH CONTENT OF STYRENE AND VINYL UNITS AND WAYS OF ITS PRODUCTION
MY179530A (en) High stiffness high impact propylene impact copolymers
MX2013006704A (en) Cleaning compositions with amphoteric polycarboxylate polymers.
JP2015535551A5 (en)
JP2010540697A5 (en)
JP2008506824A5 (en)
JP2017197739A5 (en)
JP2013528690A5 (en)
JP2010514904A5 (en)
WO2011094553A3 (en) Polyamide compositions with improved salt resistance and heat stability
JP2013507497A5 (en)
WO2012036510A3 (en) A composition comprising a monomer for polymerizing branch-type silsesquioxane polymer, branch-type silsesquioxane polymer synthesized from the same and a method for synthesizing the same