JP6662937B2 - エマルションの重合のための伸長された界面活性剤 - Google Patents
エマルションの重合のための伸長された界面活性剤 Download PDFInfo
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- JP6662937B2 JP6662937B2 JP2018064560A JP2018064560A JP6662937B2 JP 6662937 B2 JP6662937 B2 JP 6662937B2 JP 2018064560 A JP2018064560 A JP 2018064560A JP 2018064560 A JP2018064560 A JP 2018064560A JP 6662937 B2 JP6662937 B2 JP 6662937B2
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- 239000004094 surface-active agent Substances 0.000 title claims description 37
- 238000007720 emulsion polymerization reaction Methods 0.000 title description 18
- 239000000839 emulsion Substances 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 239000000178 monomer Substances 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 20
- -1 propyleneoxy group Chemical group 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 239000003505 polymerization initiator Substances 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- 150000001768 cations Chemical class 0.000 claims description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 description 18
- 239000003945 anionic surfactant Substances 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 230000000977 initiatory effect Effects 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000002245 particle Substances 0.000 description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 239000004816 latex Substances 0.000 description 5
- 229920000126 latex Polymers 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 125000005037 alkyl phenyl group Chemical group 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000002860 competitive effect Effects 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 238000004590 computer program Methods 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000004442 gravimetric analysis Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 238000003921 particle size analysis Methods 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 101100333815 Geobacillus stearothermophilus est gene Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000012527 feed solution Substances 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001511 metal iodide Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
- C08F2/24—Emulsion polymerisation with the aid of emulsifying agents
- C08F2/26—Emulsion polymerisation with the aid of emulsifying agents anionic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
- C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C309/07—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing oxygen atoms bound to the carbon skeleton
- C07C309/09—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing oxygen atoms bound to the carbon skeleton containing etherified hydroxy groups bound to the carbon skeleton
- C07C309/10—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing oxygen atoms bound to the carbon skeleton containing etherified hydroxy groups bound to the carbon skeleton with the oxygen atom of at least one of the etherified hydroxy groups further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F218/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F218/02—Esters of monocarboxylic acids
- C08F218/04—Vinyl esters
- C08F218/08—Vinyl acetate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1808—C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Polyethers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
RO−(PO)n−YZ
[式中、
RはC6〜C36の範囲にある直線状アルキル鎖、C6〜C36の範囲にある分枝アルキル鎖、またはそれらの混合物であり;
POはプロピレンオキシ基であり;
Yは−SO3、−CH2CH2CH2−SO3、−CH2CH(CH3)−SO3または−CH2COOであり;
Zはカチオンであり、そして
nは1〜50である]
をもつ、伸長された鎖をもつアニオン界面活性剤が提供される。
mixture)が使用される。
用された。試験された界面活性剤は表4に見ることができる。DISPONIL(登録商標) FES 27AおよびDOWFAX(登録商標) 2A1は競合的サンプル1として混合された。「界面活性剤1」はサンプル1として使用された。各界面活性剤の固形物は、使用されるDI水の量を調整することにより報告された。
Plus粒度分析装置上で粒度分析を実施した。各界面活性剤につき、数回の実験を実施した。凝塊パーセントおよび粒度の結果は表9に示す。
Claims (5)
- 重合開始剤および界面活性剤組成物の存在下でアクリル単量体を反応させる工程を含んでなる重合体エマルションの生成方法であって、前記界面活性剤組成物が次の式:
RO−(PO)n−YZ
[式中、
Rは、C6〜C15の範囲にあり1以上の分枝を有する分枝アルキル鎖、または、C6〜C15の範囲にある上記分枝アルキル鎖とC6〜C15の範囲にある直線状アルキル鎖の混合物であり、ここでRのアルキル分枝はC2位にあり;
POはプロピレンオキシ基であり;
Yは−SO3であり;
Zはカチオンであり、そして
nは1〜50である]
の構造を含んでなる、方法。 - RがC9〜C15の範囲にある分枝アルキル鎖とC9〜C15の範囲にある直線状アルキル鎖との混合物である、請求項1の方法。
- 重合開始剤および界面活性剤組成物の存在下でアクリル単量体またはアクリル単量体とビニルアセテート単量体の混合物を70〜80℃の温度で反応させる工程を含んでなる重合体エマルションの生成方法であって、前記界面活性剤組成物が次の式:
RO−(PO)n−YZ
[式中、
Rは、C6〜C15の範囲にあり1以上の分枝を有する分枝アルキル鎖、または、C6〜C15の範囲にある上記分枝アルキル鎖とC6〜C15の範囲にある直線状アルキル鎖の混合物であり、ここでRのアルキル分枝はC2位にあり;
POはプロピレンオキシ基であり;
Yは−SO3であり;
Zはカチオンであり、そして
nは1〜50である]
の構造を含んでなる、方法。 - 重合開始剤との反応の前に界面活性剤と単量体をプレ−エマルション中で混合する段階を更に含む、請求項3の方法。
- 単量体が3〜4時間の間に重合開始剤と界面活性剤に滴下される、請求項3の方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161526958P | 2011-08-24 | 2011-08-24 | |
US61/526,958 | 2011-08-24 |
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JP2014527320A Division JP6534812B2 (ja) | 2011-08-24 | 2012-08-24 | エマルションの重合のための伸長された界面活性剤 |
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JP2018138657A JP2018138657A (ja) | 2018-09-06 |
JP6662937B2 true JP6662937B2 (ja) | 2020-03-11 |
Family
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JP2014527320A Active JP6534812B2 (ja) | 2011-08-24 | 2012-08-24 | エマルションの重合のための伸長された界面活性剤 |
JP2018064560A Active JP6662937B2 (ja) | 2011-08-24 | 2018-03-29 | エマルションの重合のための伸長された界面活性剤 |
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US (1) | US9376509B2 (ja) |
EP (1) | EP2748249B1 (ja) |
JP (2) | JP6534812B2 (ja) |
KR (1) | KR101927789B1 (ja) |
CN (1) | CN103906804A (ja) |
BR (1) | BR112014004105B1 (ja) |
CA (1) | CA2846199C (ja) |
ES (1) | ES2739185T3 (ja) |
MX (1) | MX357130B (ja) |
PL (1) | PL2748249T3 (ja) |
WO (1) | WO2013028950A1 (ja) |
Families Citing this family (2)
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WO2013028950A1 (en) * | 2011-08-24 | 2013-02-28 | Sasol North America, Inc. | Extended surfactant for emulsion polymerization |
WO2018053738A1 (en) * | 2016-09-22 | 2018-03-29 | Rhodia Operations | Anionic surfactant and use thereof |
Family Cites Families (9)
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JPS5778936A (en) * | 1980-11-04 | 1982-05-17 | Kao Corp | Surfactant for polymer emulsion |
JP3025763B1 (ja) * | 1999-03-04 | 2000-03-27 | 花王株式会社 | 乳化重合用界面活性剤組成物 |
US7098250B2 (en) * | 2000-09-11 | 2006-08-29 | Kao Corporation | Surfactant for emulsion polymerization |
JP2003342304A (ja) * | 2002-05-30 | 2003-12-03 | New Japan Chem Co Ltd | 重合用乳化剤 |
DE102004007152A1 (de) | 2004-02-12 | 2005-08-25 | Basf Ag | Alkylethersulfate |
JP5281278B2 (ja) * | 2007-12-11 | 2013-09-04 | 花王株式会社 | 乳化重合用界面活性剤組成物 |
JP5455483B2 (ja) * | 2009-07-17 | 2014-03-26 | 花王株式会社 | 洗浄剤組成物 |
WO2012036700A1 (en) * | 2010-09-17 | 2012-03-22 | Ecolab Usa Inc. | Laundry composition for treatment of sunscreen stains based on extended chain surfactants |
WO2013028950A1 (en) * | 2011-08-24 | 2013-02-28 | Sasol North America, Inc. | Extended surfactant for emulsion polymerization |
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- 2012-08-24 BR BR112014004105-9A patent/BR112014004105B1/pt active IP Right Grant
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- 2012-08-24 EP EP12825171.7A patent/EP2748249B1/en active Active
- 2012-08-24 CN CN201280052298.XA patent/CN103906804A/zh active Pending
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BR112014004105B1 (pt) | 2020-09-15 |
US20140228530A1 (en) | 2014-08-14 |
KR20140085432A (ko) | 2014-07-07 |
BR112014004105A2 (pt) | 2017-06-06 |
PL2748249T3 (pl) | 2020-01-31 |
US9376509B2 (en) | 2016-06-28 |
EP2748249B1 (en) | 2019-05-15 |
JP6534812B2 (ja) | 2019-06-26 |
CA2846199A1 (en) | 2013-02-28 |
MX357130B (es) | 2018-06-27 |
JP2014529657A (ja) | 2014-11-13 |
MX2014002048A (es) | 2015-03-03 |
JP2018138657A (ja) | 2018-09-06 |
WO2013028950A1 (en) | 2013-02-28 |
CA2846199C (en) | 2022-06-21 |
EP2748249A1 (en) | 2014-07-02 |
CN103906804A (zh) | 2014-07-02 |
ES2739185T3 (es) | 2020-01-29 |
EP2748249A4 (en) | 2015-04-29 |
KR101927789B1 (ko) | 2018-12-12 |
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