JP2004512156A5 - - Google Patents
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- Publication number
- JP2004512156A5 JP2004512156A5 JP2002501568A JP2002501568A JP2004512156A5 JP 2004512156 A5 JP2004512156 A5 JP 2004512156A5 JP 2002501568 A JP2002501568 A JP 2002501568A JP 2002501568 A JP2002501568 A JP 2002501568A JP 2004512156 A5 JP2004512156 A5 JP 2004512156A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- structural formula
- independently
- alkyl
- linear
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- -1 oxypropylene group Chemical group 0.000 claims description 36
- 150000001875 compounds Chemical class 0.000 claims description 29
- 125000006353 oxyethylene group Chemical group 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 239000000839 emulsion Substances 0.000 claims description 12
- 125000005843 halogen group Chemical group 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 125000005647 linker group Chemical group 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 5
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 229920005682 EO-PO block copolymer Polymers 0.000 claims 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 125000001453 quaternary ammonium group Chemical group 0.000 claims 1
- 239000012071 phase Substances 0.000 description 14
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 13
- 239000000126 substance Substances 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000004094 surface-active agent Substances 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000000376 reactant Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 125000001033 ether group Chemical group 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920005906 polyester polyol Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
- 229920001807 Urea-formaldehyde Polymers 0.000 description 3
- 150000007942 carboxylates Chemical group 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000003094 microcapsule Substances 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 3
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- VVTXSHLLIKXMPY-UHFFFAOYSA-L disodium;2-sulfobenzene-1,3-dicarboxylate Chemical compound [Na+].[Na+].OS(=O)(=O)C1=C(C([O-])=O)C=CC=C1C([O-])=O VVTXSHLLIKXMPY-UHFFFAOYSA-L 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 125000000101 thioether group Chemical group 0.000 description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
- YIDSTEJLDQMWBR-UHFFFAOYSA-N 1-isocyanatododecane Chemical compound CCCCCCCCCCCCN=C=O YIDSTEJLDQMWBR-UHFFFAOYSA-N 0.000 description 1
- GFLXBRUGMACJLQ-UHFFFAOYSA-N 1-isocyanatohexadecane Chemical compound CCCCCCCCCCCCCCCCN=C=O GFLXBRUGMACJLQ-UHFFFAOYSA-N 0.000 description 1
- MGYGFNQQGAQEON-UHFFFAOYSA-N 4-tolyl isocyanate Chemical compound CC1=CC=C(N=C=O)C=C1 MGYGFNQQGAQEON-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- UJURFSDRMQAYSU-UHFFFAOYSA-N N=C=O.N=C=O.C1=CC=CC2=C(C=CC=C3)C3=C21 Chemical compound N=C=O.N=C=O.C1=CC=CC2=C(C=CC=C3)C3=C21 UJURFSDRMQAYSU-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20971700P | 2000-06-05 | 2000-06-05 | |
| US60/209,717 | 2000-06-05 | ||
| PCT/GB2001/002466 WO2001094002A2 (en) | 2000-06-05 | 2001-06-04 | Novel emulsions |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004512156A JP2004512156A (ja) | 2004-04-22 |
| JP2004512156A5 true JP2004512156A5 (OSRAM) | 2008-07-03 |
| JP5297571B2 JP5297571B2 (ja) | 2013-09-25 |
Family
ID=22779971
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002501568A Expired - Fee Related JP5297571B2 (ja) | 2000-06-05 | 2001-06-04 | 新規エマルジョン |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US6710092B2 (OSRAM) |
| EP (1) | EP1294478B1 (OSRAM) |
| JP (1) | JP5297571B2 (OSRAM) |
| AT (1) | ATE314139T1 (OSRAM) |
| AU (1) | AU7421201A (OSRAM) |
| DE (1) | DE60116303T2 (OSRAM) |
| DK (1) | DK1294478T3 (OSRAM) |
| ES (1) | ES2251487T3 (OSRAM) |
| WO (1) | WO2001094002A2 (OSRAM) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ522785A (en) * | 2000-06-05 | 2004-05-28 | Syngenta Ltd | Novel microcapsules |
| GB0103761D0 (en) * | 2001-02-15 | 2001-04-04 | Syngenta Ltd | Agrochemical formulation |
| GB0121580D0 (en) | 2001-09-06 | 2001-10-24 | Syngenta Ltd | Novel compounds |
| US7851549B2 (en) * | 2007-12-13 | 2010-12-14 | Xerox Corporation | Curable polyester latex made by phase inversion emulsification |
| GB0804700D0 (en) * | 2008-03-13 | 2008-04-16 | Syngenta Ltd | Microencapsulation |
| US8093352B2 (en) | 2008-08-05 | 2012-01-10 | Alcon Research, Ltd. | Polyalkylene oxide polyquaternary ammonium biocides |
| JP5583906B2 (ja) | 2008-12-22 | 2014-09-03 | 東レ・ダウコーニング株式会社 | 部分炭化水素基封鎖（ポリ）グリセロール変性ポリシロキサン、その製造方法、及び、当該ポリシロキサンを含む化粧料 |
| JP5430142B2 (ja) * | 2008-12-22 | 2014-02-26 | 東レ・ダウコーニング株式会社 | 乳化物の製造方法 |
| AR079413A1 (es) | 2009-10-07 | 2012-01-25 | Basf Se | Uso de particulas polimericas que comprenden insecticida para mejorar la movilidad en el suelo de insecticidas, formulaciones insecticidas, particulas polimericas que comprenden insecticida, y metodos para controlar plagas |
| WO2011137563A1 (en) | 2010-05-07 | 2011-11-10 | Unilever Plc | High solvent content emulsions |
| DE102010021688A1 (de) | 2010-05-27 | 2011-12-01 | Qineva Gmbh & Co. Kg | Verfahren zur Herstellung eines micellaren Wirkstoffkonzentrats |
| US9206381B2 (en) | 2011-09-21 | 2015-12-08 | Ecolab Usa Inc. | Reduced misting alkaline cleaners using elongational viscosity modifiers |
| US9066862B2 (en) * | 2011-11-11 | 2015-06-30 | Avon Products, Inc | Self emulsified compositions |
| ES2480343B1 (es) * | 2013-01-25 | 2015-05-20 | Ecopol Tech, S.L. | Procedimiento para la fabricación de un microencapsulado y compuesto anfifílico reactivo, microencapsulado y composición correspondientes |
| US9867763B2 (en) | 2013-05-10 | 2018-01-16 | Noxell Corporation | Modular emulsion-based product differentiation |
| US10881100B2 (en) * | 2014-01-29 | 2021-01-05 | Rotam Agrochem International Company Limited Chai Wan | Aqueous suspoemulsion containing lambda-cyhalothrin and methods for making and using the same |
| US9637708B2 (en) | 2014-02-14 | 2017-05-02 | Ecolab Usa Inc. | Reduced misting and clinging chlorine-based hard surface cleaner |
| US9745415B2 (en) * | 2014-02-21 | 2017-08-29 | Ester Industries Limited | Sulfonated co-polyesters and method for manufacturing |
| US12625134B2 (en) | 2014-10-31 | 2026-05-12 | Massachusetts Institute Of Technology | Complex liquid crystal droplets |
| WO2016070027A1 (en) * | 2014-10-31 | 2016-05-06 | Massachusetts Institute Of Technology | Compositions and methods for arranging colloid phases |
| JP6914192B2 (ja) | 2014-10-31 | 2021-08-04 | マサチューセッツ インスティテュート オブ テクノロジー | 乳剤形成のための組成および方法 |
| US10060913B2 (en) | 2016-09-19 | 2018-08-28 | Massachusetts Institute Of Technology | Systems including janus droplets capable of binding an analyte and changing orientation to provide a detectable change |
| US11119098B2 (en) | 2014-10-31 | 2021-09-14 | Massachusetts Institute Of Technology | Systems including Janus droplets |
| EP3719107B1 (en) | 2016-05-23 | 2024-08-07 | Ecolab USA Inc. | Reduced misting acidic cleaning, sanitizing, and disinfecting compositions via the use of high molecular weight water-in-oil emulsion polymers |
| CN109153947B (zh) | 2016-05-23 | 2021-03-16 | 埃科莱布美国股份有限公司 | 通过使用高分子量油包水乳液聚合物的减少雾化的碱性和中性清洁、消毒和杀菌组合物 |
| US20190170737A1 (en) | 2016-09-19 | 2019-06-06 | Massachusetts Institute Of Technology | Systems including janus droplets |
| EP3589125A1 (en) | 2017-03-01 | 2020-01-08 | Ecolab USA, Inc. | Reduced inhalation hazard sanitizers and disinfectants via high molecular weight polymers |
| MX2022000454A (es) | 2019-07-12 | 2022-04-18 | Ecolab Usa Inc | Limpiador alcalino de niebla reducida mediante el uso de polímeros en emulsión solubles en álcali. |
| BR112022004331A2 (pt) * | 2019-09-16 | 2022-08-23 | Eastman Chem Co | Emulsão, usos da emulsão e de um sulfopolímero, método para fabricar uma emulsão, e, adjuvante de emulsificação |
| US20220340709A1 (en) * | 2019-09-16 | 2022-10-27 | Eastman Chemical Company | Spreader formulation containing a sulfopolymer |
| US12446576B2 (en) | 2019-09-16 | 2025-10-21 | Eastman Chemical Company | Agrochemical formulation containing a sulfopolymer |
| US20220287300A1 (en) * | 2019-09-16 | 2022-09-15 | Eastman Chemical Company | Solvent dispersion formulation containing a sulfopolymer |
| EP4030909A4 (en) * | 2019-09-16 | 2023-09-27 | Eastman Chemical Company | SULFOPOLYMER CONTAINING DRIFT CONTROL ADJUVANT FORMULATION |
| US20220330551A1 (en) * | 2019-09-16 | 2022-10-20 | Eastman Chemical Company | Rainfastness adjuvant formulation containing a sulfopolymer |
| BR112022004526A2 (pt) * | 2019-09-16 | 2022-06-07 | Eastman Chem Co | Composição agroquímica, métodos para inibir ou matar pragas e/ou ervas daninhas ao redor de plantas e para aumentar a pegajosidade e/ou reduzir a tensão superficial, usos da composição agroquímica e de uma dispersão de sulfopolímero, e, adjuvante de pegajosidade |
| US20220361484A1 (en) * | 2019-09-16 | 2022-11-17 | Eastman Chemical Company | Rapid dispersal formulation containing a sulfopolymer |
| BR112022004709A2 (pt) * | 2019-09-16 | 2022-06-14 | Eastman Chem Co | Formulações concentrada de suspensão aquosa e de suspensão aquosa como aplicada, composição de suspensão agroquímica como aplicada, usos de um sulfopoliéster, da formulação concentrada e da composição de suspensão agroquímica, e, método |
| WO2021055092A1 (en) | 2019-09-18 | 2021-03-25 | Massachusetts Institute Of Technology | Systems and methods for affecting interactions of electromagnetic radiation with janus droplets for sensitive detection of species |
| CN116515063A (zh) * | 2023-05-29 | 2023-08-01 | 北京联合大学 | 拟除虫菊酯类农药的固相微萃取吸附剂 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3607776A (en) * | 1968-06-11 | 1971-09-21 | Pennwalt Corp | Manufacture of ingestible capsules |
| CH540715A (de) * | 1970-05-26 | 1973-10-15 | Ciba Geigy Ag | Verfahren zur Einkapselung von in einer Flüssigkeit fein verteilter Substanz |
| US3965032A (en) * | 1973-04-16 | 1976-06-22 | The Dow Chemical Company | Colloidally stable dispersions |
| GB1502777A (en) * | 1974-09-12 | 1978-03-01 | Ici Ltd | Polyurethane foams |
| US4324683A (en) * | 1975-08-20 | 1982-04-13 | Damon Corporation | Encapsulation of labile biological material |
| US4956129A (en) * | 1984-03-30 | 1990-09-11 | Ici Americas Inc. | Microencapsulation process |
| US5160529A (en) * | 1980-10-30 | 1992-11-03 | Imperial Chemical Industries Plc | Microcapsules and microencapsulation process |
| JPS62129141A (ja) * | 1985-11-29 | 1987-06-11 | Fuji Photo Film Co Ltd | マイクロカプセルの製造方法 |
| JP2569659B2 (ja) * | 1987-12-25 | 1997-01-08 | 大日本インキ化学工業株式会社 | イソシアネート化合物の乳化方法 |
| EP0336666A3 (en) * | 1988-04-04 | 1989-11-23 | Ici Americas Inc. | Polymerised substituted benzoid alkyl sulfonic acids and their salts as efficient protective colloids for microcapsulation systems |
| JP2632004B2 (ja) * | 1988-06-15 | 1997-07-16 | 富士写真フイルム株式会社 | 感圧記録シート用マイクロカプセルの製造法 |
| US5223477A (en) * | 1989-02-03 | 1993-06-29 | Imperial Chemical Industries Plc | Single-package agricultural formulations combining immediate and time-delayed delivery of thiocarbamate herbicides and dichlormid as safener |
| US5283015A (en) * | 1989-03-15 | 1994-02-01 | The Mead Corporation | Method for producing amine-formaldehyde microcapsules and photosensitive microcapsules produced thereby |
| US4977059A (en) * | 1989-05-12 | 1990-12-11 | The Mead Corporation | Sulfonated-ethylene oxide dispersants for use in preparing amine-formaldehyde microcapsules |
| US5120475A (en) * | 1989-12-14 | 1992-06-09 | The Mead Corporation | Method for preparing microcapsules having improved pre-walls, and microcapsules and photosensitive materials produced thereby |
| GB9111622D0 (en) * | 1991-05-30 | 1991-07-24 | Ici Plc | Isocyanate functional oligomer |
| DE4130743A1 (de) * | 1991-09-16 | 1993-03-18 | Bayer Ag | Mikrokapseln aus isocyanaten mit polyethylenoxidhaltigen gruppen |
| ATE156728T1 (de) * | 1992-01-03 | 1997-08-15 | Ciba Geigy Ag | Suspension von mikrokapseln und verfahren zu ihrer herstellung |
| GB9414318D0 (en) * | 1994-07-15 | 1994-09-07 | Dowelanco Ltd | Preparation of aqueous emulsions |
| DE19604466A1 (de) * | 1996-02-08 | 1997-08-14 | Basf Ag | Wässerige Zubereitungen, enthaltend Alkylpolyglykoside und ein Polymer |
| TW460508B (en) * | 1997-05-02 | 2001-10-21 | Rohm & Haas | Aqueous composition comprising a mixed surfactant/associative thickener, its use in a formulated composition, and method for enhancing thickening efficiency of aqueous composition |
| JP2906051B1 (ja) * | 1997-06-10 | 1999-06-14 | 三洋化成工業株式会社 | 乳化重合用乳化剤および樹脂水性分散体の製造方法 |
| AU5125499A (en) * | 1998-07-23 | 2000-02-14 | Huntsman Ici Chemicals Llc | Emulsifiable isocyanate compositions |
| AU770290B2 (en) * | 1998-08-06 | 2004-02-19 | National Starch And Chemical Investment Holding Corporation | Novel associative thickeners for aqueous systems |
-
2001
- 2001-06-04 WO PCT/GB2001/002466 patent/WO2001094002A2/en not_active Ceased
- 2001-06-04 DK DK01940708T patent/DK1294478T3/da active
- 2001-06-04 JP JP2002501568A patent/JP5297571B2/ja not_active Expired - Fee Related
- 2001-06-04 DE DE60116303T patent/DE60116303T2/de not_active Expired - Lifetime
- 2001-06-04 AU AU74212/01A patent/AU7421201A/en not_active Abandoned
- 2001-06-04 EP EP01940708A patent/EP1294478B1/en not_active Expired - Lifetime
- 2001-06-04 AT AT01940708T patent/ATE314139T1/de active
- 2001-06-04 ES ES01940708T patent/ES2251487T3/es not_active Expired - Lifetime
- 2001-06-05 US US09/874,955 patent/US6710092B2/en not_active Expired - Lifetime
-
2004
- 2004-03-15 US US10/800,901 patent/US7271200B2/en not_active Expired - Fee Related
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