WO2012063814A1 - ポリプロピレン系樹脂組成物 - Google Patents
ポリプロピレン系樹脂組成物 Download PDFInfo
- Publication number
- WO2012063814A1 WO2012063814A1 PCT/JP2011/075708 JP2011075708W WO2012063814A1 WO 2012063814 A1 WO2012063814 A1 WO 2012063814A1 JP 2011075708 W JP2011075708 W JP 2011075708W WO 2012063814 A1 WO2012063814 A1 WO 2012063814A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- polypropylene resin
- butyl
- tert
- bis
- ditert
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34922—Melamine; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/527—Cyclic esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2217—Oxides; Hydroxides of metals of magnesium
- C08K2003/2224—Magnesium hydroxide
Definitions
- the present invention relates to a polypropylene resin composition having improved transparency and physical strength of a polypropylene resin with a small addition amount by using an aromatic phosphate metal salt, an aromatic triamide compound and magnesium hydroxide in combination.
- Polypropylene resins such as propylene homopolymers and ethylene-propylene copolymers are widely used for automobiles, home appliances, building materials, furniture, packaging containers, toys, daily necessities, and the like.
- various nucleating agents such as benzoic acid metal salts, aromatic phosphate metal salts, metal salts of aliphatic cyclic compounds, dibenzylidene sorbitols, amide compounds, etc.
- Ingredients and clearing agents have been proposed and put into practical use.
- Patent Document 1 proposes the use of an aromatic phosphate metal salt, which shows a remarkable effect especially in improving physical strength and improves transparency.
- Patent Document 2 proposes an amide compound, and a polypropylene resin composition having excellent transparency with a small blending amount is obtained. Furthermore, the combination with other nucleating agents is suggested in paragraph (0051).
- Patent Document 3 and Patent Document 4 propose that an organic acid amide compound is used in combination with an aromatic phosphate metal salt, but the organic acid amide compound specifically described in Patent Document 3 is Both are fatty acid amide compounds, and Patent Document 4 is an amide compound derived from a divalent or higher aliphatic amine, and there is no description of an aromatic triamide compound.
- Patent Document 5 proposes that a phosphoric acid ester metal salt is used in combination with a silicate-based inorganic substance such as talc or mica.
- the nucleating agent and the clarifying agent improve various properties of the polypropylene resin, but there are additives that can be used with a low addition amount as long as the transparency is improved, such as the compound described in Patent Document 2, but the physical strength There is no improvement in the amount of the material, and there is no effect in a small amount, and it is necessary to increase the amount of addition in order to achieve high performance.
- the present invention provides a polypropylene resin composition that can suppress an increase in product price due to improved physical properties by providing a nucleating agent / clarifier composition that improves the physical strength of the polypropylene resin with a small addition amount. To do.
- an aromatic phosphate metal salt an aromatic triamide compound and magnesium hydroxide in combination, a polypropylene resin composition excellent in transparency and physical strength can be provided even with a small addition amount.
- R 1 , R 2 , R 3 and R 4 each independently represents a hydrogen atom or an alkyl group having 1 to 8 carbon atoms, and X represents a direct bond or an alkylidene group having 1 to 4 carbon atoms.
- M represents an alkali metal, an alkaline earth metal or aluminum
- Y represents a hydroxy group
- n represents 1 when M is an alkali metal
- m represents 0 or 1, 0 when M is an alkali metal or alkaline earth metal, 1 when M is aluminum and 1 when n is 2, 0 when n is 3.
- Z represents an amide bond
- R 5 , R 6 and R 7 each independently represents a linear or branched alkyl group having 1 to 8 carbon atoms.
- the transparency and physical strength of the polypropylene resin can be improved with a small amount of the nucleating agent / clarifying agent. Moreover, extraction resistance improves by the addition amount decreasing, and the sanitary property of a molded article also improves.
- polypropylene resin used in the present invention examples include propylene homopolymer, ethylene-propylene random copolymer, ethylene-propylene block copolymer, propylene and other ⁇ -olefins (for example, 1-butene, 1-hexene, 4 -Methyl-1-pentene)) and a small amount (1 to 10% by mass) of a copolymer, and a copolymer of propylene and ethylenepropylene (TPO).
- propylene homopolymer ethylene-propylene random copolymer
- ethylene-propylene block copolymer ethylene-propylene block copolymer
- propylene and other ⁇ -olefins for example, 1-butene, 1-hexene, 4 -Methyl-1-pentene
- TPO ethylenepropylene
- polypropylene resins are the types and presence / absence of polymerization catalyst / co-catalyst, stereoregularity, average molecular weight, molecular weight distribution, presence / absence and ratio of specific molecular weight components, specific gravity, viscosity, solubility in various solvents, elongation rate, impact Strength, crystallinity, X-ray diffraction, unsaturated carboxylic acids (maleic acid, itaconic acid, fumaric acid, etc.) and their derivatives (maleic anhydride, maleic acid monoester, maleic diester, etc.), organic peroxides or energy It can be used regardless of the presence or absence of modification / crosslinking treatment by irradiation of rays and a combination of these treatments.
- Examples of the alkyl group having 1 to 8 carbon atoms represented by R 1 , R 2 , R 3 and R 4 in the general formula (I) used in the present invention include, for example, methyl, ethyl, propyl, isopropyl, butyl, Secondary butyl, tertiary butyl, pentyl, tertiary pentyl, hexyl, heptyl, octyl, 2-ethylhexyl, tertiary octyl and the like.
- alkylidene group having 1 to 4 carbon atoms represented by X in the general formula (I) used in the present invention examples include methylene, ethylidene, 2,2-propylidene, 1,1-butylidene and the like.
- aromatic phosphate metal salt represented by the general formula (I) the following compound No. 1-No. 4 compounds.
- the production method of the above compound is not particularly limited, and there are no particular restrictions on the shape such as particle size and aspect ratio, and the parameters caused by the purity such as acid value and chlorine concentration, but it is excellent in dispersibility in the resin. Therefore, those having a small particle size are preferred, and those having a needle shape are preferably crushed so that the aspect ratio is small because the shrinkage ratio anisotropy of the molded product is small, and those having few impurities are preferred.
- fine powders also have drawbacks such as poor fluidity and easy generation of dust, and crushing and refining lead to increased manufacturing costs, so it is necessary to manufacture and use them for cost-effective and optimal quality. preferable.
- Examples of the linear or branched alkyl group having 1 to 8 carbon atoms represented by R 5 , R 6 and R 7 in the general formula (II) used in the present invention include, for example, methyl, ethyl, propyl, isopropyl, Examples include butyl, sec-butyl, tert-butyl, pentyl, tert-pentyl, hexyl, heptyl, octyl, 2-ethylhexyl, tert-octyl and the like.
- examples of the amide compound represented by the general formula (II) include the following compound Nos. 5-No. 7 etc. are mentioned.
- the production method of the above compound is not particularly limited, and there are no particular restrictions on the shape such as the particle size or the parameters resulting from the purity.
- the particle size is small. Those with less are preferred.
- fine powders also have drawbacks such as poor fluidity and easy generation of dust, and crushing and refining lead to increased manufacturing costs, so it is necessary to manufacture and use them for cost-effective and optimal quality. preferable.
- magnesium hydroxide used in the present invention commercially available magnesium hydroxide powder can be used as it is, and there are no particular restrictions on the shape such as particle size, the presence or absence of surface treatment, the parameters due to purity, etc.
- a particle having a small particle size is preferable because it is excellent in dispersibility in water, and a particle having few impurities is preferable.
- fine powders also have drawbacks such as poor fluidity and easy generation of dust, and crushing and refining lead to increased manufacturing costs, so it is necessary to manufacture and use them for cost-effective and optimal quality. preferable.
- the polypropylene resin composition of the present invention comprises a phenolic antioxidant, a phosphorus antioxidant, a sulfur antioxidant, a UV absorber, a hindered amine compound, a flame retardant, and a flame retardant according to the use conditions and required characteristics.
- phenolic antioxidants examples include 2,6-ditert-butyl-p-cresol, 2,6-diphenyl-4-octadecyloxyphenol, 2-methyl-4,6-bis (octylthiomethyl) phenol, Distearyl (3,5-ditert-butyl-4-hydroxybenzyl) phosphonate, 1,6-hexamethylenebis [(3,5-ditert-butyl-4-hydroxyphenyl) propionic acid amide], 4,4 '-Thiobis (6-tert-butyl-m-cresol), 2,2'-methylenebis (4-methyl-6-tert-butylphenol), 2,2'-methylenebis (4-ethyl-6-tert-butylphenol) 4,4'-butylidenebis (6-tert-butyl-m-cresol), 2,2'-ethylidenebis (4,6-ditert-butylphenol), 2,2'-ethylidenebis (4-secondary but
- phosphorus antioxidants include trisnonylphenyl phosphite, tris (2,4-ditert-butylphenyl) phosphite, tris [2-tert-butyl-4- (3-tert-butyl-4- Hydroxy-5-methylphenylthio) -5-methylphenyl] phosphite, tridecyl phosphite, octyl diphenyl phosphite, di (decyl) monophenyl phosphite, di (tridecyl) pentaerythritol diphosphite, di (nonylphenyl) ) Pentaerythritol diphosphite, bis (2,4-ditert-butylphenyl) pentaerythritol diphosphite, bis (2,6-ditert-butyl-4-methylphenyl) pentaerythritol diphosphit
- sulfur-based antioxidants include dilauryl thiodipropionate, dimyristyl thiodipropionate, dipalmityl thiodipropionate, distearyl thiodipropionate, tetrakis (methyl 3-laurylthiodipropionate) methane, Examples thereof include bis (2-methyl-4- (alkyl (C 8 -C 18 alone or in mixture) thiopropionyloxy) -5-tert-butylphenyl) sulfide, 2-mercaptobenzimidazole, and a zinc salt thereof.
- ultraviolet absorbers examples include 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-octoxybenzophenone, and 5,5′-methylenebis (2-hydroxy-4-methoxybenzophenone).
- 2-hydroxybenzophenones 2- (2′-hydroxy-5′-methylphenyl) benzotriazole, 2- (2′-hydroxy-3 ′, 5′-ditert-butylphenyl) -5-chlorobenzotriazole, 2- (2′-hydroxy-3′-tert-butyl-5′-methylphenyl) -5-chlorobenzotriazole, 2- (2′-hydroxy-5′-tert-octylphenyl) benzotriazole, 2- ( 2′-hydroxy-3 ′, 5′-dicumylphenyl) benzotriazole, 2,2′-methylenebis (4-tertiary 2- (2′-hydroxyphenyl) benzotriazoles such as til-6-benzotriazolyl)
- hindered amine compound examples include 2,2,6,6-tetramethyl-4-piperidyl stearate, 1,2,2,6,6-pentamethyl-4-piperidyl stearate, 2,2,6,6- Tetramethyl-4-piperidylbenzoate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, bis (1 -Undecyloxy-2,2,6,6-tetramethyl-4-piperidyl) carbonate, tetrakis (2,2,6,6-tetramethyl-4-piperidylbutanetetracarboxylate, tetrakis (1,2,2) , 6,6-Pentamethyl-4-piperidylbutanetetracarboxylate, bis (2,2,6,6-tetramethyl-4-piperidyl Di (tridecyl) -1,2,3,4-butanetetracarboxylate, bis (1
- Flame retardants include halogenated flame retardants such as decabromodiphenyl ether and tetrabromobisphenol A, polyphenols such as triphenyl phosphate, resorcinol and bisphenol A, and condensed phosphorus of monohydric phenols such as phenol and 2,6-xylenol. Acid esters; inorganic phosphorus compounds such as red phosphorus and melamine phosphate; nitrogen-containing flame retardants such as melamine cyanurate; inorganic flame retardants such as magnesium hydroxide and aluminum hydroxide; flame retardant aids such as antimony oxide and zirconium oxide An anti-drip agent such as polytetrafluoroethylene is used.
- halogenated flame retardants such as decabromodiphenyl ether and tetrabromobisphenol A
- polyphenols such as triphenyl phosphate, resorcinol and bisphenol A
- condensed phosphorus of monohydric phenols
- flame retardant aids include polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), polyvinyl fluoride (PVF), polytetrafluoroethylene-hexafluoropropylene copolymer (FEP), and (meth) acryl-modified PTFE.
- fluororesin such as silicon resin.
- nucleating agents include metal salts of benzoic acids such as sodium benzoate, aluminum-p-tert-butylbenzoate, lithium-p-tert-butylbenzoate; 2,2-methylenebis (4,6-ditertiary Butylphenyl) phosphate metal salts such as sodium phosphate ester; benzylidene sorbitols such as dibenzylidene sorbitol, bis (4-methylbenzylidene) sorbitol, bis (4-ethylbenzylidene) sorbitol; metal alcoholates such as glycerol zinc; Amino acid metal salts such as zinc glutamate; Aliphatic dibasic acids having a bicyclo structure such as bicycloheptane dicarboxylic acid or salts thereof and metal salts thereof; aromatic sulfonic acid metal salts such as sodium benzenesulfonate and lithium p-toluenesulfonate Etc., and the like
- heavy metal deactivator examples include 2-hydroxybenzamide-N-1H-1,2,4-triazol-3-yl and dodecandioic acid bis [2- (2-hydroxybenzoyl) hydrazide]. It is done.
- magnesium and aluminum represented by the following general formula (III), or a double salt compound comprising magnesium and aluminum is preferably used, and may be obtained by dehydrating crystal water. .
- x1, x2 and y1 each represent a number satisfying the condition represented by the following formula, and m represents 0 or an arbitrary integer. 0 ⁇ x2 / x1 ⁇ 10, 2 ⁇ x1 + x2 ⁇ 20, 0 ⁇ y1 ⁇ 2)
- the hydrotalcite compound may be a natural product or a synthetic product.
- Examples of methods for synthesizing the synthetic products include Japanese Patent Publication No. 46-2280, Japanese Patent Publication No. 50-30039, Japanese Patent Publication No. 51-29129, Japanese Patent Publication No. 3-36839, Japanese Patent Publication No. 61-174270, Examples of known synthesis methods described in JP-A-2001-164042 and JP-A-2002-53722 can be exemplified.
- the hydrotalcite compound can be used without being limited by its crystal structure, crystal particle diameter, etc., and the remaining amount of heavy metals such as iron contained in the raw material It is preferable that the purification cost is low within a practical range.
- the surface thereof is higher fatty acid such as stearic acid, higher fatty acid metal salt such as alkali metal oleate, organic sulfonic acid metal salt such as alkali metal dodecylbenzenesulfonate, higher fatty acid amide, Those coated with higher fatty acid esters or waxes can also be used.
- the obtained specimen was measured for haze using a testing machine (Toyo Seiki Seisakusho, Haze Guard 2) according to JIS K 7361-1.
- the heat distortion temperature (HDT) was measured using a testing machine (Toyo Seiki Seisakusho, automatic HDT-VICAT testing equipment) according to JIS K 7191-2, and the bending testing machine (made by Shimadzu Corporation) according to JIS K 7171. , AG-IS), and the flexural modulus (FM) was measured.
- the results are shown in Tables 1 and 2.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
(式中、x1、x2及びy1は各々下記式で表される条件を満足する数を示し、mは0又は任意の整数を示す。
0≦x2/x1≦10、2≦x1+x2<20、0≦y1≦2)
ランダムポリプロピレン(エチレン含有率2.5%、メルトフローインデックス=40)100質量部、芳香族リン酸エステル金属塩(表1参照)、アミド化合物(表1参照)、水酸化マグネシウム(表1参照)、テトラキス(3-(3,5-ジ第三ブチル-4-ヒドロキシフェニル)プロピオン酸メチル)メタン0.05、トリス(2,4-ジ第三ブチルフェニル)ホスファイト0.05質量部、カルシウムステアレート0.05質量部をヘンシェルミキサーで3分間混合し、230℃で押出し成形してペレットとし、230℃で射出成形して厚さ1mmの試験片を得た。
Claims (1)
- ポリプロピレン系樹脂100質量部に、下記一般式(I)で表される化合物0.06~0.1質量部、下記一般式(II)で表される化合物0.015~0.02質量部および水酸化マグネシウム0.015~0.03質量部を配合したことを特徴とするポリプロピレン系樹脂組成物。
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201180046807.3A CN103154121B (zh) | 2010-11-10 | 2011-11-08 | 聚丙烯系树脂组合物 |
US13/822,299 US20130172455A1 (en) | 2010-11-10 | 2011-11-08 | Polypropylene resin composition |
BR112013008989-0A BR112013008989B1 (pt) | 2010-11-10 | 2011-11-08 | Composição de resina à base de polipropileno |
KR1020137007339A KR20130122938A (ko) | 2010-11-10 | 2011-11-08 | 폴리프로필렌계 수지 조성물 |
EP11839491.5A EP2639266B1 (en) | 2010-11-10 | 2011-11-08 | Polypropylene resin composition |
AU2011327276A AU2011327276B2 (en) | 2010-11-10 | 2011-11-08 | Polypropylene resin composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010-252183 | 2010-11-10 | ||
JP2010252183A JP5722002B2 (ja) | 2010-11-10 | 2010-11-10 | ポリプロピレン系樹脂組成物 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012063814A1 true WO2012063814A1 (ja) | 2012-05-18 |
Family
ID=46050956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2011/075708 WO2012063814A1 (ja) | 2010-11-10 | 2011-11-08 | ポリプロピレン系樹脂組成物 |
Country Status (8)
Country | Link |
---|---|
US (1) | US20130172455A1 (ja) |
EP (1) | EP2639266B1 (ja) |
JP (1) | JP5722002B2 (ja) |
KR (1) | KR20130122938A (ja) |
CN (1) | CN103154121B (ja) |
AU (1) | AU2011327276B2 (ja) |
BR (1) | BR112013008989B1 (ja) |
WO (1) | WO2012063814A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015517597A (ja) * | 2012-05-22 | 2015-06-22 | ボルージュ コンパウンディング シャンハイ カンパニー リミテッド | 低反り成形物品 |
CN105209535A (zh) * | 2013-03-15 | 2015-12-30 | 百尔罗赫有限公司 | 稳定聚合物组合物及其制备方法 |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20160043930A (ko) * | 2013-08-20 | 2016-04-22 | 가부시키가이샤 아데카 | 난연성 합성수지 조성물 |
KR101499358B1 (ko) * | 2013-11-18 | 2015-03-12 | 롯데케미칼 주식회사 | 물딸림 현상이 저감된 폴리올레핀 수지 조성물 및 이를 이용하여 제조되는 성형물 |
KR102031524B1 (ko) * | 2018-05-18 | 2019-10-11 | 가부시키가이샤 아데카 | 입상 핵제, 수지 조성물, 성형품 및 그 제조 방법 |
CN110256767A (zh) * | 2019-07-26 | 2019-09-20 | 东莞市众一新材料科技有限公司 | 一种高强化粪池用塑料及其制备方法 |
Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5030039B1 (ja) | 1967-07-17 | 1975-09-27 | ||
JPS5129129B1 (ja) | 1970-12-31 | 1976-08-24 | ||
JPS59184252A (ja) | 1983-04-04 | 1984-10-19 | Adeka Argus Chem Co Ltd | ポリエステル樹脂組成物 |
JPS61174270A (ja) | 1985-01-29 | 1986-08-05 | Kyowa Chem Ind Co Ltd | 耐発錆性ないし耐着色性賦与剤 |
JPH0336839B2 (ja) | 1984-11-09 | 1991-06-03 | Mizusawa Industrial Chem | |
JPH04370124A (ja) | 1991-06-17 | 1992-12-22 | Asahi Denka Kogyo Kk | 透明性の改善された合成樹脂組成物 |
JP2001164042A (ja) | 1999-10-01 | 2001-06-19 | Toda Kogyo Corp | Mg−Al系ハイドロタルサイト型粒子粉末、塩素含有樹脂安定剤及びMg−Al系ハイドロタルサイト型粒子粉末の製造法 |
JP2002053722A (ja) | 2000-08-04 | 2002-02-19 | Toda Kogyo Corp | 塩素含有樹脂組成物 |
JP2003335968A (ja) | 2002-05-22 | 2003-11-28 | Asahi Denka Kogyo Kk | 結晶核剤組成物及びこれを含有してなる結晶性高分子組成物 |
JP2004323763A (ja) * | 2003-04-28 | 2004-11-18 | Asahi Denka Kogyo Kk | 結晶性合成樹脂組成物 |
JP2005120237A (ja) | 2003-10-16 | 2005-05-12 | Asahi Denka Kogyo Kk | 結晶核剤組成物及びこれを含有してなる結晶性高分子組成物 |
WO2005063874A1 (ja) * | 2003-12-26 | 2005-07-14 | New Japan Chemical Co., Ltd. | ポリオレフィン系樹脂の結晶化速度制御のための組成物及び方法、樹脂組成物及び樹脂成形体 |
JP2006518402A (ja) * | 2003-02-14 | 2006-08-10 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 樹脂組成物 |
WO2008075410A1 (ja) * | 2006-12-19 | 2008-06-26 | New Japan Chemical Co., Ltd. | 新規なポリオレフィン系樹脂組成物及びその樹脂成形体 |
JP2011246589A (ja) * | 2010-05-26 | 2011-12-08 | Adeka Corp | 樹脂添加剤マスターバッチ |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100344681C (zh) * | 2003-02-14 | 2007-10-24 | 西巴特殊化学品控股有限公司 | 树脂组合物 |
JP5388263B2 (ja) * | 2007-09-04 | 2014-01-15 | 株式会社Adeka | ポリオレフィン樹脂用造核剤マスターバッチ |
US8246918B2 (en) * | 2008-10-21 | 2012-08-21 | Fina Technology, Inc. | Propylene polymers for lab/medical devices |
JP5270511B2 (ja) * | 2008-10-22 | 2013-08-21 | 日本ポリプロ株式会社 | プロピレン系樹脂組成物およびその成形品 |
JP5588715B2 (ja) * | 2009-04-07 | 2014-09-10 | 日本ポリプロ株式会社 | 防曇性プロピレン系樹脂シート |
BR112012005939A2 (pt) * | 2009-09-18 | 2016-03-15 | Basf Se | composição, artigo conformado,e, uso de uma mistura |
JP2012020761A (ja) * | 2010-07-14 | 2012-02-02 | Japan Polypropylene Corp | 電気電子機器部品搬送用ケース |
-
2010
- 2010-11-10 JP JP2010252183A patent/JP5722002B2/ja active Active
-
2011
- 2011-11-08 BR BR112013008989-0A patent/BR112013008989B1/pt active IP Right Grant
- 2011-11-08 EP EP11839491.5A patent/EP2639266B1/en active Active
- 2011-11-08 WO PCT/JP2011/075708 patent/WO2012063814A1/ja active Application Filing
- 2011-11-08 US US13/822,299 patent/US20130172455A1/en not_active Abandoned
- 2011-11-08 CN CN201180046807.3A patent/CN103154121B/zh active Active
- 2011-11-08 KR KR1020137007339A patent/KR20130122938A/ko not_active Application Discontinuation
- 2011-11-08 AU AU2011327276A patent/AU2011327276B2/en active Active
Patent Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5030039B1 (ja) | 1967-07-17 | 1975-09-27 | ||
JPS5129129B1 (ja) | 1970-12-31 | 1976-08-24 | ||
JPS59184252A (ja) | 1983-04-04 | 1984-10-19 | Adeka Argus Chem Co Ltd | ポリエステル樹脂組成物 |
JPH0336839B2 (ja) | 1984-11-09 | 1991-06-03 | Mizusawa Industrial Chem | |
JPS61174270A (ja) | 1985-01-29 | 1986-08-05 | Kyowa Chem Ind Co Ltd | 耐発錆性ないし耐着色性賦与剤 |
JPH04370124A (ja) | 1991-06-17 | 1992-12-22 | Asahi Denka Kogyo Kk | 透明性の改善された合成樹脂組成物 |
JP2001164042A (ja) | 1999-10-01 | 2001-06-19 | Toda Kogyo Corp | Mg−Al系ハイドロタルサイト型粒子粉末、塩素含有樹脂安定剤及びMg−Al系ハイドロタルサイト型粒子粉末の製造法 |
JP2002053722A (ja) | 2000-08-04 | 2002-02-19 | Toda Kogyo Corp | 塩素含有樹脂組成物 |
JP2003335968A (ja) | 2002-05-22 | 2003-11-28 | Asahi Denka Kogyo Kk | 結晶核剤組成物及びこれを含有してなる結晶性高分子組成物 |
JP2006518402A (ja) * | 2003-02-14 | 2006-08-10 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 樹脂組成物 |
US7790793B2 (en) | 2003-02-14 | 2010-09-07 | Ciba Specialty Chem. Corp. | Amide nucleating agent compositions |
JP2004323763A (ja) * | 2003-04-28 | 2004-11-18 | Asahi Denka Kogyo Kk | 結晶性合成樹脂組成物 |
JP2005120237A (ja) | 2003-10-16 | 2005-05-12 | Asahi Denka Kogyo Kk | 結晶核剤組成物及びこれを含有してなる結晶性高分子組成物 |
WO2005063874A1 (ja) * | 2003-12-26 | 2005-07-14 | New Japan Chemical Co., Ltd. | ポリオレフィン系樹脂の結晶化速度制御のための組成物及び方法、樹脂組成物及び樹脂成形体 |
WO2008075410A1 (ja) * | 2006-12-19 | 2008-06-26 | New Japan Chemical Co., Ltd. | 新規なポリオレフィン系樹脂組成物及びその樹脂成形体 |
JP2011246589A (ja) * | 2010-05-26 | 2011-12-08 | Adeka Corp | 樹脂添加剤マスターバッチ |
Non-Patent Citations (1)
Title |
---|
See also references of EP2639266A4 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015517597A (ja) * | 2012-05-22 | 2015-06-22 | ボルージュ コンパウンディング シャンハイ カンパニー リミテッド | 低反り成形物品 |
CN105209535A (zh) * | 2013-03-15 | 2015-12-30 | 百尔罗赫有限公司 | 稳定聚合物组合物及其制备方法 |
US20160032078A1 (en) * | 2013-03-15 | 2016-02-04 | Baerlocher Gmbh | Stabilized polymer compositions and methods of making same |
US10119010B2 (en) * | 2013-03-15 | 2018-11-06 | Baerlocher Gmbh | Stabilized polymer compositions and methods of making same |
Also Published As
Publication number | Publication date |
---|---|
CN103154121B (zh) | 2015-08-26 |
BR112013008989A2 (pt) | 2016-07-05 |
AU2011327276B2 (en) | 2014-05-29 |
BR112013008989B1 (pt) | 2020-03-03 |
JP5722002B2 (ja) | 2015-05-20 |
EP2639266A1 (en) | 2013-09-18 |
CN103154121A (zh) | 2013-06-12 |
EP2639266B1 (en) | 2015-03-18 |
KR20130122938A (ko) | 2013-11-11 |
AU2011327276A1 (en) | 2013-04-18 |
US20130172455A1 (en) | 2013-07-04 |
JP2012102246A (ja) | 2012-05-31 |
EP2639266A4 (en) | 2014-06-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5388263B2 (ja) | ポリオレフィン樹脂用造核剤マスターバッチ | |
US9441091B2 (en) | Transparentization agent composition containing sorbitol compound and method for producing polypropylene resin composition using this sorbitol compound | |
JP5722002B2 (ja) | ポリプロピレン系樹脂組成物 | |
EP2810976B1 (en) | Resin additive masterbatch | |
EP2554586B1 (en) | Granulated resin additive composition | |
JP5628539B2 (ja) | ジベンジリデンソルビトール系透明化剤の効果を向上させた透明化剤組成物 | |
JP5461952B2 (ja) | ポリオレフィン系樹脂組成物 | |
JP2011207992A (ja) | 粒径の大きなソルビトール系透明化剤を配合したポリプロピレン系樹脂組成物の製造方法 | |
JPH0711075A (ja) | シンジオタクチックポリプロピレン組成物 | |
JP5144883B2 (ja) | プロピレン(共)重合体組成物 | |
JP5019765B2 (ja) | 樹脂添加剤マスターバッチ | |
JP2008208236A (ja) | ポリオレフィン樹脂組成物 | |
JP2006169296A (ja) | プロピレン共重合体組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 201180046807.3 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11839491 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13822299 Country of ref document: US |
|
ENP | Entry into the national phase |
Ref document number: 20137007339 Country of ref document: KR Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011839491 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 2011327276 Country of ref document: AU Date of ref document: 20111108 Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
REG | Reference to national code |
Ref country code: BR Ref legal event code: B01A Ref document number: 112013008989 Country of ref document: BR |
|
ENP | Entry into the national phase |
Ref document number: 112013008989 Country of ref document: BR Kind code of ref document: A2 Effective date: 20130412 |