JP5657004B2 - 低発泡性界面活性剤 - Google Patents
低発泡性界面活性剤 Download PDFInfo
- Publication number
- JP5657004B2 JP5657004B2 JP2012529143A JP2012529143A JP5657004B2 JP 5657004 B2 JP5657004 B2 JP 5657004B2 JP 2012529143 A JP2012529143 A JP 2012529143A JP 2012529143 A JP2012529143 A JP 2012529143A JP 5657004 B2 JP5657004 B2 JP 5657004B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- hydrogen
- range
- alkyl group
- carbon atoms
- 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.)
- Expired - Fee Related
Links
- 239000004094 surface-active agent Substances 0.000 title claims description 22
- 238000005187 foaming Methods 0.000 title claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- -1 2-ethylhexyl group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 10
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 10
- 150000001412 amines Chemical class 0.000 description 8
- 239000000080 wetting agent Substances 0.000 description 7
- 229920006395 saturated elastomer Polymers 0.000 description 6
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 150000005676 cyclic carbonates Chemical class 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000009736 wetting Methods 0.000 description 4
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 3
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000001804 emulsifying effect Effects 0.000 description 3
- 150000003673 urethanes Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 2
- 125000006165 cyclic alkyl group Chemical group 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 230000014509 gene expression Effects 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- RJLZSKYNYLYCNY-UHFFFAOYSA-N ethyl carbamate;isocyanic acid Chemical class N=C=O.CCOC(N)=O RJLZSKYNYLYCNY-UHFFFAOYSA-N 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000003918 potentiometric titration Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G71/00—Macromolecular compounds obtained by reactions forming a ureide or urethane link, otherwise, than from isocyanate radicals in the main chain of the macromolecule
- C08G71/04—Polyurethanes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09290710.4 | 2009-09-17 | ||
| EP09290710A EP2298831B1 (de) | 2009-09-17 | 2009-09-17 | Schaumarme Netzmittel |
| PCT/EP2010/005554 WO2011032664A2 (de) | 2009-09-17 | 2010-09-09 | Schaumarme tenside |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013505306A JP2013505306A (ja) | 2013-02-14 |
| JP2013505306A5 JP2013505306A5 (cg-RX-API-DMAC7.html) | 2013-10-24 |
| JP5657004B2 true JP5657004B2 (ja) | 2015-01-21 |
Family
ID=41478836
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012529143A Expired - Fee Related JP5657004B2 (ja) | 2009-09-17 | 2010-09-09 | 低発泡性界面活性剤 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8629297B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2298831B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5657004B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN102498154B (cg-RX-API-DMAC7.html) |
| BR (1) | BR112012005836A2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2011032664A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014124123A1 (en) * | 2013-02-06 | 2014-08-14 | Encell Technology, Inc. | Nickel iron battery employing untreated polyolefin separator with a surfactant in the electrolyte |
| CA2891948A1 (en) * | 2013-07-22 | 2015-01-29 | Huntsman Petrochemical Llc | Polymeric surfactant |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5011A (en) * | 1847-03-13 | V boring-machine | ||
| US2236119A (en) | 1939-09-30 | 1941-03-25 | Linde Air Prod Co | Mold coating |
| DE1768058A1 (de) * | 1967-04-03 | 1971-12-09 | Gaf Corp | Antistatika aus der Carbamatreihe sowie Verfahren zu deren Herstellung |
| GB1402182A (en) * | 1968-12-30 | 1975-08-06 | Ici Ltd | Nitrogen-containing siloxane oxyalkylene copolymers |
| DE2416206A1 (de) * | 1974-04-03 | 1975-10-16 | Bayer Ag | Antistatische polyamidmassen, ihre verwendung und verfahren zu ihrer herstellung |
| US4500655A (en) * | 1983-12-29 | 1985-02-19 | Texaco Inc. | Alkoxylated modified Mannich condensates and manufacture of rigid polyurethane foams therewith |
| JPS63501576A (ja) * | 1985-08-09 | 1988-06-16 | ユニオン カ−バイド コ−ポレ−シヨン | カルバメ−トコ−テイング組成物 |
| US4883854A (en) * | 1988-09-30 | 1989-11-28 | Medtronic, Inc. | Hydroxyl functional monomers |
| DE4101158C2 (de) * | 1991-01-14 | 1994-06-23 | Dainippon Ink & Chemicals | Wärmehärtbare Reaktionsharzgemische, Verwendung der erfindungsgemäßen Reaktionsharze zur Herstellung von Formkörpern und Beschichtungen |
| US6646153B1 (en) * | 2000-07-19 | 2003-11-11 | E. I. Du Pont De Nemours And Company | Hydroxyl functional urethanes having a tertiary carbamate bond |
| AT409967B (de) * | 2000-10-17 | 2002-12-27 | Solutia Austria Gmbh | Zweikomponentensysteme auf basis von wasserlöslichen polyestern und verkappten isocyanaten zur formulierung von wasserverdünnbaren einbrennlacken |
| WO2003066580A1 (en) * | 2002-02-07 | 2003-08-14 | Ucb, S.A. | Process using a cyclic carbonate reactant |
| DE10257094A1 (de) * | 2002-12-05 | 2004-06-24 | Basf Ag | Enzymatische Herstellung urethangruppenhaltiger (Meth)acrylsäureester |
| US7329773B2 (en) | 2002-12-12 | 2008-02-12 | Surface Specialties, S.A. | Process for producing carbamoyloxy (meth) acrylates and new carbamoyloxy (meth)acrylates |
| WO2004074352A2 (en) | 2003-02-19 | 2004-09-02 | Virginia Tech Intellectual Properties, Inc. | Carbonation of epoxidized vegetable oils and nonisocyanate-polyurethanes derived therefrom |
| US20040236119A1 (en) | 2003-04-24 | 2004-11-25 | Jurgen Van Holen | Process using a cyclic carbonate reactant and beta-hydroxyurethanes thereby obtained |
| EP1652891B1 (en) * | 2003-07-18 | 2012-06-13 | Konishi Co., Ltd. | Curable resin composition and cold-setting adhesive |
| JP2007538021A (ja) | 2004-05-17 | 2007-12-27 | サイテック サーフェース スペシャリティーズ、エス．エイ． | ウレタン（メタ）アクリレートの製造法及び新規なウレタン（メタ）アクリレート |
-
2009
- 2009-09-17 EP EP09290710A patent/EP2298831B1/de active Active
-
2010
- 2010-09-09 JP JP2012529143A patent/JP5657004B2/ja not_active Expired - Fee Related
- 2010-09-09 CN CN201080041278.3A patent/CN102498154B/zh active Active
- 2010-09-09 BR BR112012005836A patent/BR112012005836A2/pt not_active IP Right Cessation
- 2010-09-09 WO PCT/EP2010/005554 patent/WO2011032664A2/de not_active Ceased
- 2010-09-09 US US13/395,968 patent/US8629297B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP2298831A1 (de) | 2011-03-23 |
| CN102498154B (zh) | 2014-04-16 |
| US8629297B2 (en) | 2014-01-14 |
| EP2298831B1 (de) | 2013-02-20 |
| WO2011032664A3 (de) | 2011-09-15 |
| BR112012005836A2 (pt) | 2017-09-12 |
| WO2011032664A2 (de) | 2011-03-24 |
| CN102498154A (zh) | 2012-06-13 |
| JP2013505306A (ja) | 2013-02-14 |
| US20120172618A1 (en) | 2012-07-05 |
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