TW201118163A - Acetylated derivatives of castor oil and their blends with epoxidized fatty acid esters - Google Patents
Acetylated derivatives of castor oil and their blends with epoxidized fatty acid esters Download PDFInfo
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- TW201118163A TW201118163A TW99133015A TW99133015A TW201118163A TW 201118163 A TW201118163 A TW 201118163A TW 99133015 A TW99133015 A TW 99133015A TW 99133015 A TW99133015 A TW 99133015A TW 201118163 A TW201118163 A TW 201118163A
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- Prior art keywords
- plasticizer
- composition
- component
- acid
- acetylated
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- PLSARIKBYIPYPF-UHFFFAOYSA-H trimagnesium dicitrate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O PLSARIKBYIPYPF-UHFFFAOYSA-H 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- JNXDCMUUZNIWPQ-UHFFFAOYSA-N trioctyl benzene-1,2,4-tricarboxylate Chemical compound CCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCC)C(C(=O)OCCCCCCCC)=C1 JNXDCMUUZNIWPQ-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 235000013976 turmeric Nutrition 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 229940124543 ultraviolet light absorber Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
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- 238000011179 visual inspection Methods 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
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- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0016—Plasticisers
-
- 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
- C08K5/0091—Complexes with metal-heteroatom-bonds
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1515—Three-membered rings
-
- 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
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/443—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from vinylhalogenides or other halogenoethylenic compounds
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/17—Protection against damage caused by external factors, e.g. sheaths or armouring
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/1355—Elemental metal containing [e.g., substrate, foil, film, coating, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31692—Next to addition polymer from unsaturated monomers
- Y10T428/31699—Ester, halide or nitrile of addition polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Insulated Conductors (AREA)
- Organic Insulating Materials (AREA)
- Paints Or Removers (AREA)
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| JP3037530B2 (ja) | 1992-11-17 | 2000-04-24 | 新日本製鐵株式会社 | レ形開先多層溶接における裏波溶接ビードのルート止端部の折れ込み防止方法 |
| MX2010008963A (es) | 2008-02-15 | 2011-02-24 | Union Carbide Chem Plastic | Sistema plastificante de reemplazo para formulaciones plastificadas con ftalato. |
| CA2775975C (en) | 2009-09-30 | 2016-11-08 | Dow Global Technologies Llc | Heat stabilized polymeric composition with epoxidized fatty acid ester plasticizer |
| US8802988B2 (en) | 2009-09-30 | 2014-08-12 | Dow Global Technologies Llc | Acetylated derivatives of castor oil and their blends with epoxidized fatty acid esters |
| US8552098B2 (en) | 2009-09-30 | 2013-10-08 | Dow Global Technologies Llc | Purified acetylated derivatives of castor oil and compositions including same |
| JP5693589B2 (ja) | 2009-09-30 | 2015-04-01 | ダウ グローバル テクノロジーズ エルエルシー | １２−ヒドロキシステアリン酸のアセチル化グリセリドおよびエポキシ化脂肪酸エステルとのブレンド |
| CN102985481A (zh) | 2010-05-10 | 2013-03-20 | 陶氏环球技术有限责任公司 | 由源自可再生资源的增塑剂制备的挠性pvc组合物 |
| TW201209168A (en) | 2010-07-28 | 2012-03-01 | Dow Global Technologies Llc | Plasticizers made from oil extracted from microorganisms and polar polymeric compositions comprising the same |
| US9056965B2 (en) | 2011-09-30 | 2015-06-16 | Dow Global Technologies Llc | Process for mixing polyvinyl chloride with a bio-based plasticizer |
| CA2850429C (en) * | 2011-09-30 | 2020-06-02 | Dow Global Technologies Llc | Plasticizer for low temperature unwind with weight retention during heat aging |
| JP5673569B2 (ja) * | 2012-01-17 | 2015-02-18 | 日立金属株式会社 | 絶縁電線 |
| MX357165B (es) | 2012-02-08 | 2018-06-28 | Dow Global Technologies Llc | Composiciones de plastificante y metodos para fabricar composiciones de plastificante. |
| CN104379653B (zh) | 2012-06-22 | 2017-07-18 | 陶氏环球技术有限责任公司 | 乙酰化多元醇羟基硬脂酸酯增塑剂和经增塑的聚合物组合物 |
| EP2864406B1 (en) | 2012-06-26 | 2017-03-08 | Dow Global Technologies LLC | Plasticizers and plasticized polymeric compositions |
| MX370205B (es) | 2012-10-18 | 2019-12-05 | Dow Global Technologies Llc | Plastificantes de alquil esteres de acidos grasos epoxidados y metodos para hacer plastificantes de alquil esteres de acidos grasos epoxidados. |
| KR102017370B1 (ko) | 2012-11-12 | 2019-09-02 | 다우 글로벌 테크놀로지스 엘엘씨 | 에폭시화 지방산 알킬 에스테르 가소제 및 에폭시화 지방산 알킬 에스테르 가소제의 제조 방법 |
| JP6189967B2 (ja) | 2012-11-12 | 2017-08-30 | ダウ グローバル テクノロジーズ エルエルシー | エポキシ化脂肪酸アルキルエステルを作製するための方法 |
| CN110256857B (zh) * | 2012-12-29 | 2022-01-04 | 美国圣戈班性能塑料公司 | 柔性管 |
| WO2014163871A1 (en) * | 2013-03-11 | 2014-10-09 | Dow Global Technologies Llc | Synergistic blends of calcium carbonate and calcined clay |
| WO2014197327A1 (en) | 2013-06-03 | 2014-12-11 | Regents Of The University Of Minnesota | Epoxy estolide fatty acid alkyl esters useful as biorenewable plasticizers |
| JP6524105B2 (ja) * | 2013-10-02 | 2019-06-05 | ダウ グローバル テクノロジーズ エルエルシー | 生物可塑剤及び可塑化ポリマー組成物 |
| DK3033753T3 (en) * | 2013-10-23 | 2019-03-25 | Prysmian Spa | Energy cable with a cross-linked electrical insulating layer and method for extracting cross-linked by-products therefrom |
| RU2704009C2 (ru) | 2015-04-22 | 2019-10-23 | Призмиан С.П.А. | Силовой кабель с системой сшитой электрической изоляции и способ его изготовления с извлечением побочных продуктов сшивания |
| US10144812B2 (en) | 2015-10-05 | 2018-12-04 | Regents Of The University Of Minnesota | Multi-functional fatty acid ester derivatives useful as biorenewable plasticizers |
| KR101833175B1 (ko) | 2016-06-15 | 2018-02-27 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
| KR101833174B1 (ko) | 2016-06-15 | 2018-02-27 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
| KR101981990B1 (ko) * | 2016-12-30 | 2019-05-24 | 한국화학연구원 | 천연계 카다놀 기반 가소제 및 식물유 기반 에폭시화 가소제를 포함하는 가소제 조성물, 및 이를 포함하는 고분자 수지 조성물 |
| EP4097177A1 (en) * | 2020-01-30 | 2022-12-07 | Cargill, Incorporated | Plasticizer composition and process to produce a plasticizer composition |
| JP7784788B2 (ja) * | 2022-03-25 | 2025-12-12 | 株式会社松風 | 歯科用研磨材 |
| CN115612030B (zh) * | 2022-10-27 | 2025-10-10 | 中国林业科学研究院林产化学工业研究所 | 一种蓖麻油基阻燃增塑剂及其制备方法 |
| WO2025128797A1 (en) | 2023-12-13 | 2025-06-19 | Blue Evolution, Inc | Ecofriendly, biodegradable biological polysaccharide composition for packaging materials |
Family Cites Families (121)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR499931A (fr) * | 1917-12-08 | 1920-02-26 | Twitchell Process C | Sulfonate de métaux alcalins et son procédé de fabrication |
| US2397592A (en) * | 1940-08-02 | 1946-04-02 | Gen Cable Corp | Resinous compositions for wire coatings and the like |
| US2403215A (en) | 1943-10-14 | 1946-07-02 | Du Pont | Resinous compositions and electrical conductors insulated therewith |
| US2458484A (en) | 1946-06-17 | 1949-01-04 | Gen Mills Inc | Process of preparing epoxy derivatives from unsaturated aliphatic compounds |
| US2666752A (en) | 1950-01-17 | 1954-01-19 | Sherwin Williams Co | Stabilizer for halogen-containing polymers |
| US2618622A (en) | 1950-01-17 | 1952-11-18 | Sherwin Williams Co | Plasticizer for vinyl halides |
| GB790314A (en) | 1955-02-23 | 1958-02-05 | Lankro Chem Ltd | New derivatives or acetylated castor oil and esters of acetylated ricinoleic acid, and polymers plasticised therewith |
| GB934689A (en) | 1959-04-22 | 1963-08-21 | Swift & Co | Epoxy fatty acid esters and polyvinyl resin compositions containing them |
| NL131832C (enExample) | 1959-11-12 | |||
| US3138566A (en) | 1960-01-08 | 1964-06-23 | Gen Mills Inc | Fluid resins prepared from epoxidized unsaturated fatty acids or esters |
| BE647338A (enExample) | 1963-05-01 | 1964-10-30 | ||
| FR1437722A (fr) | 1964-04-03 | 1966-05-06 | Allied Chem | Compositions à base de polymères vinyliques servant de revêtement du sol |
| US3409580A (en) * | 1964-05-01 | 1968-11-05 | Ethyl Corp | Polyvinyl halide plastisols containing cyclohexyl amines and cellular products therefrom |
| NL127901C (enExample) | 1966-02-10 | |||
| US3639318A (en) | 1968-05-29 | 1972-02-01 | Union Carbide Corp | Plasticized polyvinyl chloride film |
| DE2009047C2 (de) | 1970-02-26 | 1982-04-08 | Degussa Ag, 6000 Frankfurt | Verfahren zur Herstellung von Epoxystearinsäureestern |
| DE2021530A1 (de) | 1970-05-02 | 1971-11-25 | Henkel & Cie Gmbh | Verfahren zur Herstellung von Oxyfettsaeureestern |
| US3891694A (en) | 1970-05-18 | 1975-06-24 | Monsanto Co | Plasticizer purification |
| US3668091A (en) | 1971-02-02 | 1972-06-06 | Ashland Oil Inc | Ultraviolet light bleaching of carboxylic acid esters and epoxy compounds |
| US3712875A (en) | 1971-02-22 | 1973-01-23 | Union Carbide Corp | Synergistic additive system for anti-fog vinyl film |
| US3780140A (en) | 1971-08-06 | 1973-12-18 | Du Pont | Ethylene/carbon monoxide polymer compositions |
| US3868341A (en) | 1972-06-02 | 1975-02-25 | Western Electric Co | Clear flame retardant composition |
| US3872187A (en) | 1972-09-18 | 1975-03-18 | Tenneco Chem | Aryloxyalkyl haloalkyl phosphates |
| GB1415770A (en) | 1972-09-18 | 1975-11-26 | Tenneco Chem | Falme-retardant phosphate esters and flame retardant resinous compositions |
| US4083816A (en) | 1976-06-25 | 1978-04-11 | The United States Of America As Represented By The Secretary Of Agriculture | Acetoxymethyl derivatives of polyunsaturated fatty triglycerides as primary plasticizers for polyvinylchloride |
| DE2652328A1 (de) | 1976-11-17 | 1978-05-18 | Neynaber Chemie Gmbh | Bleiverbindungen enthaltende stabilisator-gleitmittel-kombination fuer formmassen auf basis von polyvinylchlorid |
| US4346145A (en) | 1981-01-05 | 1982-08-24 | Western Electric Co., Inc. | Coating composition and coated articles |
| DE3125376A1 (de) | 1981-06-27 | 1983-01-13 | Hoechst Ag, 6000 Frankfurt | Thermoplastische formmassen auf der basis von vinylchloridpolymerisaten und schlagzaehmodifizierungspolymeren |
| JPS5832647A (ja) | 1981-08-21 | 1983-02-25 | Riken Vitamin Co Ltd | 熱可塑性樹脂組成物 |
| US4627993A (en) | 1982-07-01 | 1986-12-09 | E. I. Du Pont De Nemours And Company | Thermoplastic elastomeric compositions based on compatible blends of an ethylene copolymer and vinyl or vinylidene halide polymer |
| US4613533A (en) | 1982-07-01 | 1986-09-23 | E. I. Du Pont De Nemours And Company | Thermoplastic elastomeric compositions based on compatible blends of an ethylene copolymer and vinyl or vinylidene halide polymer |
| DE3326455A1 (de) | 1983-07-22 | 1985-01-31 | Henkel Kgaa | Kosmetisch-pharmazeutische oelkomponenten |
| JPS6133661A (ja) | 1984-02-02 | 1986-02-17 | テルモ株式会社 | 医療用器具 |
| JPS6116950U (ja) | 1984-07-05 | 1986-01-31 | 河西工業株式会社 | 自動車用インシユレ−タダツシユ |
| US4556694A (en) | 1984-07-26 | 1985-12-03 | E. I. Du Pont De Nemours And Company | Low temperature flexible PVC blends |
| JPS6169851A (ja) * | 1984-09-12 | 1986-04-10 | Shin Etsu Polymer Co Ltd | 食品包装フイルム用塩化ビニル系樹脂組成物 |
| DE3503383A1 (de) | 1985-02-01 | 1986-08-07 | Hoechst Ag, 6230 Frankfurt | Folie auf basis von vinylchloridpolymerisat und ihre verwendung zur herstellung steifer rohrfoermiger koerper |
| JPS61212201A (ja) | 1985-03-15 | 1986-09-20 | 富士ロビン株式会社 | センタドライブ型ロ−タリ作業機におけるロ−タリ作業部の構造 |
| US4670494A (en) | 1985-07-30 | 1987-06-02 | Gary Chemical Corp. | Flame retardant low smoke poly(vinyl chloride) thermoplastic composition |
| US4605694A (en) | 1985-10-31 | 1986-08-12 | Hercules Incorporated | Plasticizing compositions for polyvinylchloride |
| US4857600A (en) | 1988-05-23 | 1989-08-15 | Union Carbide Corporation | Process for grafting diacid anhydrides |
| US5036121A (en) | 1988-09-06 | 1991-07-30 | The B. F. Goodrich Company | Flame and smoke retardant cable insulation and jacketing compositions |
| AU610013B2 (en) | 1988-09-09 | 1991-05-09 | B.F. Goodrich Company, The | Flexible blend compositions based on overpolymers of vinyl chloride polymers on ethylene copolymers |
| JPH0354233A (ja) | 1989-04-19 | 1991-03-08 | Furukawa Electric Co Ltd:The | 複合難燃剤およびそれを含有する難燃性樹脂組成物 |
| HU209937B (en) | 1989-05-04 | 1994-12-28 | Du Pont | Polyvinyl chloride composition and calendered sheet prepared from it |
| US5225108A (en) | 1990-05-18 | 1993-07-06 | Witco Corporation | Polymer stabilizer and polymer composition stabililzed therewith |
| AU8025991A (en) | 1990-07-20 | 1992-01-23 | B.F. Goodrich Company, The | Improved barrier pvc resins, compounds and articles derived therefrom |
| JPH0485354U (enExample) | 1990-11-30 | 1992-07-24 | ||
| JPH04261452A (ja) | 1991-02-15 | 1992-09-17 | Asahi Denka Kogyo Kk | 農業用塩化ビニル系樹脂組成物 |
| US5246783A (en) | 1991-08-15 | 1993-09-21 | Exxon Chemical Patents Inc. | Electrical devices comprising polymeric insulating or semiconducting members |
| US5227417A (en) | 1992-01-24 | 1993-07-13 | Cooper Industries, Inc. | Polyvinyl chloride based plenum cable |
| US5484844A (en) | 1992-04-14 | 1996-01-16 | Mitsubishi Chemical Mkv Company | Vinyl chloride resin elastomer composition |
| JPH07508066A (ja) | 1992-05-19 | 1995-09-07 | クロンプトン・コーポレーション | 鉛ではない安定剤を用いて安定化した電気絶縁用の塩化ビニル樹脂組成物 |
| US5466267A (en) | 1992-09-17 | 1995-11-14 | Mobil Oil Corporation | Oligomeric/polymeric multifunctional additives to improve the low-temperature properties of distillate fuels |
| US5454806A (en) | 1992-11-06 | 1995-10-03 | Terumo Kabushiki Kaisha | Medical device |
| US5270366A (en) | 1992-12-16 | 1993-12-14 | Vista Chemical Company | Lead stabilized, flexible polymeric blends containing polyvinylchloride |
| US5886072A (en) | 1993-05-24 | 1999-03-23 | Teknor Apex Company | Flame retardant composition |
| US5430108A (en) | 1994-01-14 | 1995-07-04 | Exxon Chemical Patents Inc. | Polyol ester PVC plasticizers |
| US5495033A (en) | 1994-08-29 | 1996-02-27 | Cenex/Land O'lakes Agronomy Company | Methylated herbicidal adjuvant |
| US5464903A (en) | 1994-10-31 | 1995-11-07 | E. I. Du Pont De Nemours And Company | Process for preparing ethylene copolymer plasticized PVC |
| US5575965A (en) | 1995-05-19 | 1996-11-19 | Union Carbide Chemicals & Plastics Technology Corporation | Process for extrusion |
| JP3036405B2 (ja) | 1995-06-14 | 2000-04-24 | 三菱化学エムケーブイ株式会社 | 塩化ビニル系樹脂組成物 |
| US5929133A (en) | 1996-02-16 | 1999-07-27 | Hitachi Chemical Filtec, Inc. | Anti-bacterial film suitable for food packaging |
| US5686147A (en) * | 1996-11-18 | 1997-11-11 | The Goodyear Tire & Rubber Company | Plastisol composition |
| US6063846A (en) | 1997-05-30 | 2000-05-16 | Teknor Apex Company | Polyvinyl chloride compositions |
| US6114425A (en) | 1997-07-17 | 2000-09-05 | Unitex Chemical Corporation | Plasticized polyvinyl chloride compound |
| US5753772A (en) * | 1997-07-17 | 1998-05-19 | The Goodyear Tire & Rubber Company | Rubbery polymers with improved color stability |
| US6274750B1 (en) | 1998-07-21 | 2001-08-14 | Cognis Corporation | Dimer and trimer acid esters from epoxidized compounds and methods for their preparation |
| BR9917230A (pt) | 1999-04-21 | 2002-01-08 | Basf Ag | Mistura de diésteres de nonanol isomérico de um ácido dicarboxìlico, e, uso da mesma |
| JP2000319468A (ja) | 1999-05-07 | 2000-11-21 | Asahi Denka Kogyo Kk | 塩化ビニル系樹脂用安定剤組成物 |
| US6496629B2 (en) | 1999-05-28 | 2002-12-17 | Tycom (Us) Inc. | Undersea telecommunications cable |
| DK1624014T3 (da) | 1999-08-19 | 2010-01-11 | Danisco | Specifikke acylerede glycerolforbindelser som blödgöringsmidler i polymerer og fremgangsmåde til deres fremstilling |
| US6949597B2 (en) | 1999-08-19 | 2005-09-27 | Danisco A/S | Composition |
| US6608142B1 (en) | 2000-05-08 | 2003-08-19 | Teknor Apex Company | Polyvinyl chloride compositions |
| US6797753B2 (en) | 2000-06-20 | 2004-09-28 | Battelle Memorial Institute | Plasticizers derived from vegetable oils |
| CN1341681A (zh) | 2000-09-07 | 2002-03-27 | 苏州德威实业有限公司 | 用于电线电缆的软聚氯乙烯塑料 |
| US6451958B1 (en) | 2001-04-06 | 2002-09-17 | Sartomer Technology Company Inc. | Radiation curable acrylate-terminated polymers having polycarbonate repeating units |
| JP2003064233A (ja) | 2001-08-27 | 2003-03-05 | C I Kasei Co Ltd | 農業用塩化ビニル系樹脂フィルム及び塩化ビニル系樹脂組成物 |
| US6706815B2 (en) | 2001-09-06 | 2004-03-16 | Dupont Dow Elastomers L.L.C. | Impact resistant rigid PVC compositions using hydrocarbon rubbers and chlorinated polyethylene as impact modifiers |
| US6849694B2 (en) | 2002-01-17 | 2005-02-01 | Dupont Dow Elastomers, Llc | Impact modifier compositions for rigid PVC compositions of hydrocarbon rubbers and chlorinated polyethylene |
| US6714707B2 (en) | 2002-01-24 | 2004-03-30 | Alcatel | Optical cable housing an optical unit surrounded by a plurality of gel layers |
| JP2003297149A (ja) | 2002-04-04 | 2003-10-17 | Fujikura Ltd | 電気絶縁性ポリ塩化ビニル樹脂組成物 |
| US6869985B2 (en) | 2002-05-10 | 2005-03-22 | Awi Licensing Company | Environmentally friendly polylactide-based composite formulations |
| JP4204305B2 (ja) | 2002-11-08 | 2009-01-07 | 株式会社Ａｄｅｋａ | ポリエステル系可塑剤及び塩素含有樹脂組成物 |
| WO2004052978A1 (en) | 2002-12-06 | 2004-06-24 | Cognis Brasil Ltda. | Plasticizer compositions for nitrocellulose based resins |
| WO2004052977A1 (en) | 2002-12-06 | 2004-06-24 | Cognis Brasil Ltda. | Plasticized poly vinyl chloride compositions |
| US7015285B2 (en) | 2002-12-18 | 2006-03-21 | General Electric | Composition and method for improving the adhesion of polyphenylene ether moldings to polyurethane foam |
| US20040122149A1 (en) | 2002-12-19 | 2004-06-24 | Kadakia Vishal S. | Flame-retardant polyvinyl chloride compositions |
| JP2004311064A (ja) | 2003-04-02 | 2004-11-04 | Fujikura Ltd | 直流電力ケーブル |
| US20050058674A1 (en) * | 2003-09-11 | 2005-03-17 | Kimberly-Clark Worldwide, Inc. | Moisturizing and lubricating compositions |
| JP4640753B2 (ja) | 2003-12-08 | 2011-03-02 | 株式会社Adeka | 塩化ビニル系樹脂組成物 |
| FR2880892B1 (fr) | 2005-01-17 | 2008-03-21 | Gerflor Sa | Utilisation d'acides gras esterifies comme plastifiants du pvc |
| JP2006282999A (ja) * | 2005-03-11 | 2006-10-19 | Kureha Corp | 塩化ビニリデン系樹脂組成物及びそれからなるフィルム |
| JP2006335874A (ja) * | 2005-06-02 | 2006-12-14 | Kao Corp | 生分解性樹脂用可塑剤 |
| DE102005031945A1 (de) | 2005-07-08 | 2007-01-11 | Construction Research & Technology Gmbh | Verwendung von entfärbtem Biodiesel als Weichmacher |
| DE102005059143A1 (de) | 2005-12-08 | 2007-06-14 | J. S. Staedtler Gmbh & Co. Kg | Modelliermasse sowie deren Verwendung |
| CN101108982A (zh) | 2006-07-21 | 2008-01-23 | 时代环保能源集团（香港）投资有限公司 | 一种用生物柴油制取的塑料环保增塑剂 |
| JP5094109B2 (ja) | 2006-12-22 | 2012-12-12 | 株式会社Ａｄｅｋａ | 塩化ビニル系樹脂組成物 |
| GB0700074D0 (en) | 2007-01-03 | 2007-02-07 | Danisco | process |
| GB0700076D0 (en) | 2007-01-03 | 2007-02-07 | Danisco | Compound |
| US20080227993A1 (en) | 2007-03-17 | 2008-09-18 | Matthew Mark Zuckerman | Synthesizing and compounding molecules from and with plant oils to improve low temperature behavior of plant oils as fuels, oils and lubricants |
| EP1978013A1 (en) | 2007-04-04 | 2008-10-08 | Cognis IP Management GmbH | Diols and polyols |
| CN100590188C (zh) | 2007-05-22 | 2010-02-17 | 江阴市向阳科技有限公司 | 利用废弃油脂生产环氧增塑剂的方法 |
| EP2223970B1 (en) | 2007-11-28 | 2014-03-26 | Adeka Corporation | Stabilizer for chlorine-containing resins and chlorine -containing resin compositions |
| BRPI0705621B1 (pt) | 2007-12-10 | 2019-04-09 | Nexoleum Bioderivados Ltda. | Composição plastificte de pvc |
| BRPI0705276A2 (pt) | 2007-12-10 | 2009-08-11 | Nexoleum Bioderivados Ltda | plastificantes primários de pvc derivados de óleos vegetais, processo de obtenção de plastificantes primários de pvc derivados de oléos vegetais e composição de pvc plastificado |
| MX2010008963A (es) | 2008-02-15 | 2011-02-24 | Union Carbide Chem Plastic | Sistema plastificante de reemplazo para formulaciones plastificadas con ftalato. |
| JP5254363B2 (ja) * | 2008-02-15 | 2013-08-07 | ザ プロクター アンド ギャンブル カンパニー | ポリプロピレングリコール材料を含むローションを備える吸収性物品 |
| MX341364B (es) | 2008-06-17 | 2016-08-18 | Resinas Y Mat S A De C V | Bioplastificantes o plastificantes oleoquimicos primarios, que a su vez actuan como estabilizadores termicos y de radiacion ultravioleta en resinas moldeables de pvc y proceso para obtencion de los mismos. |
| JP2010042669A (ja) | 2008-07-16 | 2010-02-25 | Daikin Ind Ltd | フッ素ゴム積層体およびその製造方法 |
| CN101343380B (zh) * | 2008-09-02 | 2011-06-01 | 山东蓝帆塑胶股份有限公司 | 一种制备增塑剂的方法 |
| CN101591588A (zh) | 2009-06-24 | 2009-12-02 | 江南大学 | 有机铼氧化物-过氧化脲催化制备环氧大豆油或环氧脂肪酸甲(乙)酯的方法 |
| FR2950051B1 (fr) | 2009-09-11 | 2012-08-03 | Centre Nat Rech Scient | Nouveau procede de preparation de polyols et produits tels qu'obtenus |
| US8552098B2 (en) | 2009-09-30 | 2013-10-08 | Dow Global Technologies Llc | Purified acetylated derivatives of castor oil and compositions including same |
| JP5693589B2 (ja) * | 2009-09-30 | 2015-04-01 | ダウ グローバル テクノロジーズ エルエルシー | １２−ヒドロキシステアリン酸のアセチル化グリセリドおよびエポキシ化脂肪酸エステルとのブレンド |
| CN102666697B (zh) | 2009-09-30 | 2015-01-07 | 陶氏环球技术有限责任公司 | 乙酰基化的聚甘油脂肪酸酯以及用其增塑的聚氯乙烯绝缘材料 |
| US8802988B2 (en) | 2009-09-30 | 2014-08-12 | Dow Global Technologies Llc | Acetylated derivatives of castor oil and their blends with epoxidized fatty acid esters |
| CN101824193B (zh) | 2010-02-24 | 2013-01-30 | 杭州高新橡塑材料股份有限公司 | 一种耐寒pvc电缆料及制备方法 |
| CN102985481A (zh) | 2010-05-10 | 2013-03-20 | 陶氏环球技术有限责任公司 | 由源自可再生资源的增塑剂制备的挠性pvc组合物 |
| CN101914219B (zh) | 2010-07-26 | 2012-09-05 | 江阴市向阳科技有限公司 | 一种复合环氧增塑剂的制备方法 |
| WO2013003225A2 (en) | 2011-06-29 | 2013-01-03 | Dow Global Technologies Llc | Vegetable-oil derived plasticizer |
-
2010
- 2010-09-29 US US13/498,745 patent/US8802988B2/en active Active
- 2010-09-29 JP JP2012532263A patent/JP5841946B2/ja active Active
- 2010-09-29 BR BR112012007266-8A patent/BR112012007266B1/pt active IP Right Grant
- 2010-09-29 EP EP20100765709 patent/EP2483341B1/en active Active
- 2010-09-29 WO PCT/US2010/050676 patent/WO2011041380A1/en not_active Ceased
- 2010-09-29 MX MX2012003941A patent/MX2012003941A/es active IP Right Grant
- 2010-09-29 KR KR1020127011003A patent/KR101904553B1/ko active Active
- 2010-09-29 CA CA2775930A patent/CA2775930C/en active Active
- 2010-09-29 CN CN201080054110.6A patent/CN102648237B/zh active Active
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Also Published As
| Publication number | Publication date |
|---|---|
| US20120181061A1 (en) | 2012-07-19 |
| BR112012007266B1 (pt) | 2021-03-09 |
| US20140323622A1 (en) | 2014-10-30 |
| US9181415B2 (en) | 2015-11-10 |
| US8802988B2 (en) | 2014-08-12 |
| MX2012003941A (es) | 2012-06-19 |
| CA2775930A1 (en) | 2011-04-07 |
| CN102648237B (zh) | 2015-04-22 |
| EP2483341A1 (en) | 2012-08-08 |
| JP5841946B2 (ja) | 2016-01-13 |
| KR20120085270A (ko) | 2012-07-31 |
| CA2775930C (en) | 2017-02-14 |
| WO2011041380A1 (en) | 2011-04-07 |
| EP2483341B1 (en) | 2013-07-17 |
| CN102648237A (zh) | 2012-08-22 |
| BR112012007266A2 (pt) | 2020-08-11 |
| KR101904553B1 (ko) | 2018-10-04 |
| JP2013506736A (ja) | 2013-02-28 |
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