JP2019513867A - ポリアルキレンオキシド基及び第四級窒素原子を含むコポリマー - Google Patents
ポリアルキレンオキシド基及び第四級窒素原子を含むコポリマー Download PDFInfo
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- JP2019513867A JP2019513867A JP2018553118A JP2018553118A JP2019513867A JP 2019513867 A JP2019513867 A JP 2019513867A JP 2018553118 A JP2018553118 A JP 2018553118A JP 2018553118 A JP2018553118 A JP 2018553118A JP 2019513867 A JP2019513867 A JP 2019513867A
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- methyl
- monomer
- meth
- monoethylenically unsaturated
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- 229920001577 copolymer Polymers 0.000 title claims abstract description 48
- 229920000233 poly(alkylene oxides) Polymers 0.000 title claims abstract description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 title abstract 2
- 239000000178 monomer Substances 0.000 claims abstract description 66
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 19
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 13
- 239000001257 hydrogen Substances 0.000 claims abstract description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 125000000129 anionic group Chemical group 0.000 claims abstract description 10
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims abstract description 3
- 150000004820 halides Chemical class 0.000 claims abstract description 3
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims description 39
- -1 ethylene, propylene Chemical group 0.000 claims description 24
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 125000002091 cationic group Chemical group 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 abstract description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 8
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- 238000001542 size-exclusion chromatography Methods 0.000 description 7
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- 238000005406 washing Methods 0.000 description 5
- RJFMWUISYZMHPA-UHFFFAOYSA-N 1-ethenyl-3-methyl-1,2-dihydroimidazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.CN1C[NH+](C=C)C=C1 RJFMWUISYZMHPA-UHFFFAOYSA-N 0.000 description 4
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
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- 230000000694 effects Effects 0.000 description 3
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- 235000013772 propylene glycol Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
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- BZVFPIHTRLNAQA-UHFFFAOYSA-M 1-ethenyl-3-methylimidazol-3-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C[N+]=1C=CN(C=C)C=1 BZVFPIHTRLNAQA-UHFFFAOYSA-M 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
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- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
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- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
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- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
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- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
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- 239000003960 organic solvent Substances 0.000 description 1
- 125000005385 peroxodisulfate group Chemical group 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
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- DQJSKCFIYCTPBV-UHFFFAOYSA-N propan-2-yl n-(propan-2-yloxycarbonylamino)peroxycarbamate Chemical compound CC(C)OC(=O)NOONC(=O)OC(C)C DQJSKCFIYCTPBV-UHFFFAOYSA-N 0.000 description 1
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- BHRKTJMAZMWXOS-UHFFFAOYSA-N propyl 2-methylprop-2-enoate;trimethylazanium;chloride Chemical compound [Cl-].C[NH+](C)C.CCCOC(=O)C(C)=C BHRKTJMAZMWXOS-UHFFFAOYSA-N 0.000 description 1
- OMCBATFUNZDGIA-UHFFFAOYSA-N propyl prop-2-enoate;trimethylazanium;chloride Chemical compound [Cl-].C[NH+](C)C.CCCOC(=O)C=C OMCBATFUNZDGIA-UHFFFAOYSA-N 0.000 description 1
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- LDTLADDKFLAYJA-UHFFFAOYSA-L sodium metabisulphite Chemical compound [Na+].[Na+].[O-]S(=O)OS([O-])=O LDTLADDKFLAYJA-UHFFFAOYSA-L 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- KOUDKOMXLMXFKX-UHFFFAOYSA-N sodium oxido(oxo)phosphanium hydrate Chemical compound O.[Na+].[O-][PH+]=O KOUDKOMXLMXFKX-UHFFFAOYSA-N 0.000 description 1
- 159000000000 sodium salts Chemical group 0.000 description 1
- 239000008234 soft water Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
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- 238000004381 surface treatment Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
- OHOTVSOGTVKXEL-UHFFFAOYSA-K trisodium;2-[bis(carboxylatomethyl)amino]propanoate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C(C)N(CC([O-])=O)CC([O-])=O OHOTVSOGTVKXEL-UHFFFAOYSA-K 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
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- 229920001567 vinyl ester resin Polymers 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 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
- 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
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Abstract
Description
Xは、Yが−O−である場合−CH2−又は−CO−であり;
Yが−NH−である場合−CO−であり;
Yは、−O−又は−NH−であり;
R1は、水素又はメチルであり;
R2は、同一又は異なるC2〜C6−アルキレンラジカルであり、直鎖状又は分岐状でよく、ブロック状に又は無作為に配置されてよく;
R3は、水素又はC1〜C4−アルキルであり;
nは、25〜75、好ましくは45〜70、より好ましくは45〜65、より好ましくは50〜65、最も好ましくは51〜65の整数である)
の少なくとも1種のモノエチレン性不飽和ポリアルキレンオキシドモノマー、
(B)1〜40質量%の少なくとも1つの四級化窒素含有モノエチレン性不飽和モノマー、
(C)0〜10質量%のアニオン性モノエチレン性不飽和モノマー、並びに
(D)0〜30質量%の他の非イオン性モノエチレン性不飽和モノマー
を共重合した形態で含み、>100,000の平均分子量Mwを有する新規コポリマーに関する。
(A)60〜99質量%の式I
Xは、Yが−O−である場合−CH2−又は−CO−であり;
Yが−NH−である場合−CO−であり;
Yは、−O−又は−NH−であり;
R1は、水素又はメチルであり;
R2は、同一又は異なるC2〜C6−アルキレンラジカルであり、直鎖状又は分岐状でよく、ブロック状に又は無作為に配置されてよく;
R3は、水素又はC1〜C4−アルキルであり;
nは、25〜75、好ましくは45〜70、より好ましくは45〜65、より好ましくは50〜65、最も好ましくは51〜65の整数である)
の少なくとも1種のモノエチレン性不飽和ポリアルキレンオキシドモノマー(モノマー(A))、
(B)1〜40質量%の少なくとも1つの四級化窒素含有モノエチレン性不飽和モノマー(モノマー(B))、
(C)0〜10質量%のアニオン性モノエチレン性不飽和モノマー(モノマー(C))、並びに
(D)0〜30質量%の他の非イオン性モノエチレン性不飽和モノマー(モノマー(D))
を共重合した形態で含み、
>100,000の平均分子量Mwを有する新規コポリマーによって達成されることが見出された。一実施形態では、本発明のコポリマーは、>100,000〜1,000,000の、>100,000〜750,000の、>100,000〜500,000の、>100,000〜400,000の、又は>100,000〜300,000の質量平均分子量Mwを有する。質量平均分子量の上限は、本発明のコポリマーの所望の粘度に依存し、粘度は質量平均分子量が増加するにつれて増加する。
Xは、−CO−であり;
Yは、−O−であり;
R1は、水素又はメチルであり;
R2は、ブロック状に又は無作為に配置された同一又は異なる直鎖状又は分岐状のC2〜C6−アルキレンラジカルであり、好ましくはエチレン、1,2−又は1,3−プロピレン又はその混合物であり、特に好ましくはエチレンであり;
R3は、メチルであり;
nは、5〜30の整数である。
− (メタ)アクリル酸と、末端がキャップされておらず、一端がアルキルラジカルでキャップされ、一端がアミノ化されている、又は一端がアルキルラジカルでキャップされ、一端がアミノ化されているポリアルキレングリコールとの反応生成物;
− 末端がキャップされていない、又は一端がアルキル、フェニル又はアルキルフェニルラジカルでキャップされているポリアルキレングリコールのアルキルエーテルである。
− メチルポリエチレングリコール(メタ)アクリレート及び(メタ)アクリルアミド、メチルポリプロピレングリコール(メタ)アクリレート及び(メタ)アクリルアミド、メチルポリブチレングリコール(メタ)アクリレート及び(メタ)アクリルアミド、メチルポリ(プロピレンオキシド−co−エチレンオキシド)(メタ)アクリレート及び(メタ)アクリルアミド、エチルポリエチレングリコール(メタ)アクリレート及び(メタ)アクリルアミド、エチルポリプロピレングリコール(メタ)アクリレート及び(メタ)アクリルアミド、エチルポリブチレングリコール(メタ)アクリレート及び(メタ)アクリルアミド及びエチルポリ(プロピレンオキシド−co−エチレンオキシド)(メタ)アクリレート及び(メタ)アクリルアミド、いずれも3〜50個の、好ましくは3〜30個の、特に好ましくは5〜30個のアルキレンオキシド単位を有し、メチルポリエチレングリコールアクリレートが好ましく、メチルポリエチレングリコールメタクリレートが特に好ましい;
− エチレングリコールアリルエーテル及びメチルエチレングリコールアリルエーテル、プロピレングリコールアリルエーテル及びメチルプロピレングリコールアリルエーテル、いずれも3〜50個の、好ましくは3〜30個の、特に好ましくは5〜30個のアルキレンオキシド単位を有する。
Rは、C1〜C4−アルキル又はベンジル、好ましくはメチル、エチル又はベンジルであり;
R’は、水素又はメチルであり;
Yは、−O−又は−NH−であり;
Aは、C1〜C6−アルキレン、好ましくは直鎖又は分岐C2〜C4−アルキレン、特に1,2−エチレン、1,3−及び1,2−プロピレン又は1,4−ブチレンであり;
X_は、ハライド、例えばイオダイド及び好ましくはクロライド又はブロマイド、C1〜C4−アルキルサルフェート、好ましくはメチルサルフェート又はエチルサルフェート、C1〜C4−アルキルスルホネート、好ましくはメチルスルホネート又はエチルスルホネート、及びC1〜C4−アルキルカーボネートである。
− 3−メチル−1−ビニルイミダゾリウムクロライド、3−メチル−1−ビニルイミダゾリウムメチルサルフェート、3−エチル−1−ビニルイミダゾリウムエチルサルフェート、3−エチル−1−ビニルイミダゾリウムクロライド及び3−ベンジル−1−ビニルイミダゾリウムクロライド;
− 1−メチル−4−ビニルピリジニウムクロライド、1−メチル−4−ビニルピリジニウムメチルサルフェート及び1−ベンジル−4−ビニルピリジニウムクロライド;
− メタクリルアミドプロピルトリメチルアンモニウムクロライド、メタクリルアミドエチルトリメチルアンモニウムクロライド、トリメチルアンモニウムエチルアクリレートクロライド及びメチルサルフェート、トリメチルアンモニウムエチルメタクリレートクロライド及びメチルサルフェート、ジメチルエチルアンモニウムエチルアクリレートエチルサルフェート、ジメチルエチルアンモニウムエチルメタクリレートエチルサルフェート、トリメチルアンモニウムプロピルアクリレートクロライド及び−メチルサルフェート及びトリメチルアンモニウムプロピルメタクリレートクロライド及びメチルサルフェート;
− ジメチルジアリルアンモニウムクロライド及びジエチルジアリルアンモニウムクロライド
が含まれる。
− 好ましくは3〜6個の炭素原子を有するα、β−不飽和モノカルボン酸、例えばアクリル酸、メタクリル酸、エタクリル酸、クロトン酸及びビニル酢酸、好ましくはアクリル酸及びメタクリル酸;
− 好ましくは4〜6個の炭素原子を有する不飽和ジカルボン鎖、例えばイタコン酸及びマレイン酸、その無水物、例えば無水マレイン酸;
− エチレン性不飽和スルホン酸、例えばビニルスルホン酸、アクリルアミドプロパンスルホン酸、メタアリルスルホン酸、メタクリルスルホン酸、m−及びp−スチレンスルホン酸、(メタ)アクリルアミドメタンスルホン酸、(メタ)アクリルアミドエタンスルホン酸、(メタ)アクリルアミドプロパンスルホン酸、2−(メタ)アクリルアミド−2−メチルプロパンスルホン酸、2−アクリルアミド−2−ブタンスルホン酸、3−メタクリルアミド−2−ヒドロキシプロパンスルホン酸、メタンスルホン酸アクリレート、エタンスルホン酸アクリレート、プロパンスルホン酸アクリレート、アリルオキシベンゼンスルホン酸、メタリルオキシベンゼンスルホン酸及び1−アリルオキシ−2−ヒドロキシプロパンスルホン酸;
− エチレン性不飽和ホスホン酸、例えばビニルホスホン酸並びにm−及びp−スチレンホスホン酸;
− C2〜C4−アルキレングリコールモノ(メタ)アクリレート及びポリ(C2〜C4−アルキレン)グリコールモノ(メタ)アクリレートの酸性ホスフェートエステル、例えばエチレングリコールモノ(メタ)アクリレート、プロピレングリコールモノ(メタ)アクリレート、ポリエチレングリコールモノ(メタ)アクリレート及びポリプロピレングリコールモノ(メタ)アクリレート
である。
− モノエチレン性不飽和C3〜C6−カルボン酸、特にアクリル酸及びメタクリル酸と、一価C1〜C22−アルコール、特にC1〜C16−アルコールとのエステル;及びモノエチレン性不飽和C3〜C6カルボン酸、特にアクリル酸及びメタクリル酸と、二価C2〜C4−アルコールとのヒドロキシアルキルエステル、例えばメチル(メタ)アクリレート、エチル(メタ)アクリレート、n−ブチル(メタ)アクリレート、sec−ブチル(メタ)アクリレート、tert−ブチル(メタ)アクリレート、エチルヘキシル(メタ)アクリレート、デシル(メタ)アクリレート、ラウリル(メタ)アクリレート、イソボルニル(メタ)アクリレート、セチル(メタ)アクリレート、パルミチル(メタ)アクリレート及びステアリル(メタ)アクリレート、ヒドロキシエチル(メタ)アクリレート、ヒドロキシプロピル(メタ)アクリレート及びヒドロキシブチル(メタ)アクリレート;
− モノエチレン性不飽和C3〜C6−カルボン酸、特にアクリル酸及びメタクリル酸と、C1〜C12−アルキルアミン及びジ(C1〜C4−アルキル)アミンとのアミド、例えばN−メチル(メタ)アクリルアミド、N,N−ジメチル(メタ)アクリルアミド、N−エチル(メタ)アクリルアミド、N−プロピル(メタ)アクリルアミド、N−tert−ブチル(メタ)アクリルアミド、N−tert−オクチル(メタ)アクリルアミド及びN−ウンデシル(メタ)アクリルアミド、及び(メタ)アクリルアミド;
− 飽和C2〜C30−カルボン酸、特にC2〜C14−カルボン酸のビニルエステル、例えばビニルアセテート、ビニルプロピオネート、ビニルブチレート、ビニル2−エチルヘキサノエート及びビニルラウレート;
− ビニルC1〜C30−アルキルエーテル、特にビニルC1〜C18−アルキルエーテル、例えばビニルメチルエーテル、ビニルエチルエーテル、ビニルn−プロピルエーテル、ビニルイソプロピルエーテル、ビニルn−ブチルエーテル、ビニルイソブチルエーテル、ビニル2−エチヘキシルエーテル、及びビニルオクタデシルエーテル;
− N−ビニルアミド及びN−ビニルラクタム、例えばN−ビニルホルムアミド、N−ビニル−N−メチルホルムアミド、N−ビニルアセトアミド、N−ビニル−N−メチルアセトアミド、N−ビニルピロリドン、N−ビニルピペリドン及びN−ビニルカプロラクタム;
− 脂肪族及び芳香族オレフィン、例えばエチレン、プロピレン、C4〜C24−α−オレフィン、特にC4〜C16−α−オレフィン、例えばブチレン、イソブチレン、ジイソブテン、スチレン及びα−メチルスチレン、並びに活性二重結合を有するジオレフィン、例えば、ブタジエン;
− 不飽和ニトリル、例えばアクリロニトリル及びメタアクリロニトリル
が含まれる。
重合は大気圧下で行うことが好ましい。しかし、それはまた、発生する自生的圧力の下で閉鎖系で実施することもできる。
GPC(SEC)法:
ポリマーの質量平均分子量Mw及び数平均分子量Mnは、サイズ排除クロマトグラフィー(SEC)の技術によって決定した。SEC分離条件は、3つの親水性ビニルポリマーネットワークゲルカラムで、0.1%(w/w)トリフルオロ酢酸/0.1M NaClの存在する蒸留水中35℃であった。較正は、分子量Mw=620〜Mw=2.070.000を有する狭分散性ポリ(2−ビニルピリジン)−標準(PSS社、ドイツ)を用いて行った。
MPEG−MA/QVI、80/20質量%、EO単位約45個
4Lの攪拌容器中に水(838.5g)を仕込み、窒素流下で90℃まで加熱した。水(12.15g)中のWako V50(1.35g、和光純薬工業株式会社製)の溶液を4時間かけて添加し、分子量約2000g/molを有するメトキシポリエチレングリコールメタクリレート(50%、1080g、Visiomer MPEG2005MA W、Evonik Industries社製)及び3−メチル−1−ビニル−1H−イミダゾリウム−メチル−サルフェート(「QVI」、45%、300g、BASF SE社製)の溶液を3時間かけて添加した。流れが両方とも終了した後、重合混合物をこの温度でさらに30分間維持した。続いて、水(30.38g)中のWako V50(3.38g)の溶液を15分間かけて添加して1時間撹拌し、次いで放置して室温まで冷却した。GPCから、Mw=143,000g/mol及びMn=30,300g/molの値を得た。
MPEG3000、RD199517、GM0006−53を有するADW;MPEG−MA/QVI、80/20質量%、EO単位約65個
2Lの攪拌容器中に水(374.9g)を仕込み、窒素流下で90℃まで加熱した。水(12.31g)中のWako V50(0.65g、和光純薬工業株式会社製)の溶液を4時間かけて添加し、分子量約3000g/molを有するメトキシポリエチレングリコールメタクリレート(50%、518.4g)及び3−メチル−1−ビニル−1H−イミダゾリウム−メチル−サルフェート(45%、144g、BASF SE社製)の溶液を3時間かけて添加した。流れが両方とも終了した後、重合混合物をこの温度でさらに30分間維持した。続いて、水(30.78g)中のWako V50(1.62g)の溶液を1時間かけて添加し、次いで放置して室温まで冷却した。GPCから、Mw=138,000g/mol及びMn=10,900g/molの値を得た。
80/20 MPEG−MA/QVI、EO単位約45個
2Lの攪拌容器中に水(152.61g)及びナトリウムハイポホスファイトモノヒドレート(0.61g)を仕込み、窒素流下で90℃まで加熱した。水(21.14g)中のナトリウムペルオキソジサルフェート(2.35g)の溶液を4時間かけて添加し、分子量約2000g/molを有するメトキシポリエチレングリコールメタクリレート(50%、648g)及び3−メチル−1−ビニル−1H−イミダゾリウム−メチル−サルフェート(45%、188.1g)の溶液を3時間かけて添加した。流れが両方とも終了した後、重合混合物をこの温度でさらに30分間維持した。続いて、水(18.23g)中のナトリウムペルサルフェート(2.03g)の溶液を15分間かけて添加して1時間撹拌し、次いで放置して室温まで冷却した。GPCから、Mw=116,000g/mol及びMn=4,190g/molの値を得た。
80/20 MPEG EO45/QVI、MW100,000
4Lの攪拌容器中に水(280.8g)を仕込み、窒素流下で90℃まで加熱した。水(24.00g)中のWako V50(2.40g、和光純薬工業株式会社製)の溶液を4時間かけて添加し、分子量約2000g/molを有するメトキシポリエチレングリコールメタクリレート(50%、384.00g、Visiomer MPEG2005MA W、Evonik Industries社製)及び3−メチル−1−ビニル−1H−イミダゾリウム−メチル−サルフェート(45%、106.67g、BASF SE社製)の溶液を3時間かけて添加した。流れが両方とも終了した後、重合混合物をこの温度でさらに30分間維持した。続いて、水(12.00g)中のWako V50(1.20g)の溶液を15分間かけて添加して1時間撹拌し、次いで放置して室温まで冷却した。GPCから、Mw=100,000g/molの値を得た。
80/20 MPEG EO45/QVI、MW179,000
4Lの攪拌容器中に水(312.45g)を仕込み、窒素流下で90℃まで加熱した。水(26.46g)中のWako V50(0.27g、和光純薬工業株式会社製)の溶液を4時間かけて添加し、分子量約2000g/molを有するメトキシポリエチレングリコールメタクリレート(50%、432.00g、Visiomer MPEG2005MA W、Evonik Industries社製)及び3−メチル−1−ビニル−1H−イミダゾリウム−メチル−サルフェート(45%、120.00g、BASF SE社製)の溶液を3時間かけて添加した。流れが両方とも終了した後、重合混合物をこの温度でさらに30分間維持した。続いて、水(13.50g)中のWako V50(1.35g)の溶液を15分間かけて添加して1時間撹拌し、次いで放置して室温まで冷却した。GPCから、Mw=179,000g/mol及びMn=32,900g/molの値を得た。
以下の食器洗浄組成物、本発明によるコポリマーを含む組成物A、C及びE、並びに本発明の範囲外の比較参考例としての組成物B及びDを調製した。該組成物は、二重区画の水溶性の袋を重ね合わせて作製した。一方の区画は固体組成物を、他方の区画は液体組成物を含有した。
スルホン化ポリマー Rohm&Haas社供給のAcusol588
漂白活性化剤 テトラアセチルエチレンジアミン
漂白触媒 ペンタアミノコバルトアセテートニトレート
非イオン性界面活性剤1 Plurafac SLF180、BASF社供給
非イオン性界面活性剤2 LutensolTO7、BASF社供給
HEDP 1−ヒドロキシエタン1,1−ジホスホン酸
例P1のポリマー EO45個を有する80質量%のMPEG及び20質量%のQVI、Mw143,000
コポリマーD EO45個を有する80質量%のMPEG及び20質量%のQVI、Mw179,000
コポリマー3 EO45個を有する95質量%のMPEG及び5質量%のQVI、Mw10,800(本発明の範囲外)
2. ジャガイモデンプンに水を加え、ゲルが形成されるまで平鍋で加熱する。平鍋を室温で一晩放置して冷ます。
3. ケチャップとマスタードをボウルに加え、Blixer Coupe 5VV(速度6)を使用して完全に混ざるまで1分間激しく混合する。
4. 電子レンジ(全出力750W)で、マーガリン(1分)、ラード(2分)及びベーキングスプレッド(1分)を個別に溶かし、室温まで冷却(15分)した後、合わせて激しく混合する。
5. 小麦粉と安息香酸をボウルに加え、激しく混合する。
6. 卵(大)5〜6個をボウルに割り入れ、激しく混合する(1分)。
7. 卵219gをボウルに秤量する。植物油219gを卵に加え、ハンドブレンダーを使用してかき混ぜる(1分間)。
8. クリームと牛乳をボウルに入れて混ぜる(1分)。
9. すべての材料を一緒に大きな容器に加え、激しく混合する(10分)。
10. この混合物の50g分をプラスチック製のつぼに秤量して凍らせる。
2. ゆっくりと粉乳を加え連続的に攪拌する。
3. 混合物を冷まし、固化したら、ハンドブレンダーで混合して混合物を均質化する。
4. 冷蔵庫に保管する。
Miele社食器洗い機を使用し、通常洗浄50℃の設定でマルチサイクル試験を行った。各サイクルにおいて、洗浄開始時に50gの汚れ1を食器洗浄機に添加し、さらに、50gのマーガリン−牛乳汚れを2つのスチール製平鍋(25g/平鍋)上に広げ、バラスト(ballast)として一番下のバスケットに加えた。水硬度は20US gpgであった。
北米Maytag社食器洗浄機を用いて2回目のマルチサイクル試験を行った。注入水を55℃に予熱し、洗浄サイクルを55℃で通常洗浄に設定した。各サイクルにおいて、洗浄開始時に50gの汚れ1を食器洗浄機に添加し、さらに、50gのマーガリン−牛乳汚れを2つのスチール製平鍋(25g/平鍋)上に広げ、バラストとして一番下のバスケットに加えた。注入水は、CaCl2及びMgCl2塩で21US gpgまでスパイクした脱イオン水であり、Ca:Mgモル比は3:1であった。スチレン/アクリロニトリルタンブラー2個も試験に含め、これらは前処理せずに新品から洗浄した。
Claims (5)
- (A)60〜99質量%の式I
Xは、Yが−O−である場合−CH2−又は−CO−であり;
Yが−NH−である場合−CO−であり;
Yは、−O−又は−NH−であり;
R1は、水素又はメチルであり;
R2は、同一又は異なるC2〜C6−アルキレンラジカルであり、ブロック状に又は無作為に配置されてよく;
R3は、水素又はC1〜C4−アルキルであり;
nは、25〜75の整数である)
の少なくとも1種のモノエチレン性不飽和ポリアルキレンオキシドモノマー、
(B)式IIaからIId
(式中、変数は以下の意味を有する:
Rは、C1〜C4−アルキル又はベンジルであり;
R’は、水素又はメチルであり;
Yは、−O−又は−NH−であり;
Aは、C1〜C6−アルキレンであり;
X_は、ハライド、C1〜C4−アルキルサルフェート、C1〜C4−アルキルスルホネート及びC1〜C4−アルキルカーボネートである)、
(C)0〜10質量%のアニオン性モノエチレン性不飽和モノマー、並びに
(D)0〜30質量%の他の非イオン性モノエチレン性不飽和モノマー
を共重合した形態で含み、>100,000の平均分子量Mwを有するコポリマー。 - 前記式I
(式中、変数は以下の意味を有する:
Xは、−CO−であり;
Yは、−O−であり;
R1は、水素又はメチルであり;
R2は、エチレン、プロピレン又はその混合物であり;
R3は、メチルであり;
nは、51〜65の整数である)
の少なくとも1種のモノマーを、モノマー(A)として共重合した形態で含む、請求項1に記載のコポリマー。 - 60〜98質量%のモノマー(A)、1〜39質量%のモノマー(B)及び1〜39質量%のモノマー(C)を共重合した形態で含む、請求項1又は2に記載のコポリマー。
- (A)の(B)に対する質量比が≧2:1であり、前記コポリマーがモノマー(C)を共重合した形態で含む場合、(B)の(C)に対する質量比も≧2:1である、請求項1から3のいずれか一項に記載のコポリマー。
- 前記コポリマーの全体的な正味電荷がカチオン性である、請求項1から4のいずれか一項に記載のコポリマー。
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US (1) | US10815327B2 (ja) |
EP (1) | EP3440121B1 (ja) |
JP (1) | JP2019513867A (ja) |
KR (1) | KR20180135894A (ja) |
CN (1) | CN108884197A (ja) |
BR (1) | BR112018070486A2 (ja) |
CA (1) | CA3018136A1 (ja) |
ES (1) | ES2808285T3 (ja) |
MX (1) | MX2018012317A (ja) |
PL (1) | PL3440121T3 (ja) |
RU (1) | RU2736718C2 (ja) |
WO (1) | WO2017174468A1 (ja) |
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WO2004055075A1 (en) * | 2002-12-13 | 2004-07-01 | Unilever Plc | Polymers and laundry detergent compositions containing them |
JP2007510806A (ja) * | 2003-11-21 | 2007-04-26 | ザ プロクター アンド ギャンブル カンパニー | ポリアルキレンオキシド基及び四級窒素原子を含有するコポリマー並びに界面活性剤系を有する洗濯組成物 |
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RU2736718C2 (ru) | 2020-11-19 |
ES2808285T3 (es) | 2021-02-26 |
US20190359751A1 (en) | 2019-11-28 |
CN108884197A (zh) | 2018-11-23 |
BR112018070486A2 (pt) | 2019-01-29 |
US10815327B2 (en) | 2020-10-27 |
RU2018139015A (ru) | 2020-05-12 |
CA3018136A1 (en) | 2017-10-12 |
MX2018012317A (es) | 2019-02-20 |
PL3440121T3 (pl) | 2020-11-02 |
EP3440121A1 (en) | 2019-02-13 |
EP3440121B1 (en) | 2020-05-06 |
KR20180135894A (ko) | 2018-12-21 |
RU2018139015A3 (ja) | 2020-05-14 |
WO2017174468A1 (en) | 2017-10-12 |
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