JP5657004B2 - 低発泡性界面活性剤 - Google Patents
低発泡性界面活性剤 Download PDFInfo
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- 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
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- 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.)
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- 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)
Description
R1は、水素、炭素数1〜3のアルキル基または基R3であり、
R2は、直鎖、分枝または環状であってよく、飽和、モノオレフィン性不飽和またはポリオレフィン性不飽和であってもよい炭素数2〜22のアルキル基であり、
R3は、炭素数1〜3の飽和アルキル基であり、このアルキル基は、1つの炭素原子において基−O−(CH2−CHZ−O)p−Hにより置換されており、
X、YおよびZは、互いに独立に、水素またはメチル基であり、
nおよびmは、互いに独立して、1〜45の範囲の数であり、pは、0〜45の数である(ただし、n+m+pの合計は、2〜70の範囲になければならない)〕
で示される化合物を提供する。
R1は、水素、炭素数1〜3のアルキル基または基R3であり、
R2は、直鎖、分枝または環状であってよく、飽和、モノオレフィン性不飽和またはポリオレフィン性不飽和であってもよい炭素数2〜22のアルキル基であり、
R3は、炭素数1〜3の飽和アルキル基であり、このアルキル基は、1つの炭素原子において基−O−(CH2−CHZ−O)p−Hにより置換されており、
X、YおよびZは、互いに独立に、水素またはメチル基であり、
nおよびmは、互いに独立して、1〜45の範囲の数であり、pは、0〜45の数である(ただし、n+m+pの合計は、2〜70の範囲になければならない)。
化合物(I)は、−(CH2−CHX−O)n−、−(CH2−CHY−O)m−、および−(CH2−CHZ−O)p−〔それぞれ、前記条件が適用される〕の構造単位を含む。
基R2は、炭素数2〜22、好ましくは6〜14のアルキル基であり、このアルキル基は、
− 直鎖、分枝または環状、
− 飽和、モノオレフィン性不飽和またはポリオレフィン性不飽和
であってよい。
Claims (8)
- 請求項1に記載の構造(I)で示される化合物の低発泡性界面活性剤としての使用。
- 基R1が水素である請求項2に記載の使用。
- 基R1が炭素数1〜3のアルキル基である請求項2に記載の使用。
- 基X、YおよびZの全てが水素である請求項2に記載の使用。
- n+m+pの合計が10〜25の範囲にある請求項2〜5のいずれかに記載の使用。
- 基R1が水素であり;基X、YおよびZの全てが水素であり;n+m+pの合計(p=0である)が10〜25の範囲にある、請求項2に記載の使用。
- 基R1が基R3〔R3はCH2OHを意味する〕であり;基X、YおよびZの全てが水素であり;n+m+pの合計(p=0である)が10〜25の範囲にある、請求項2に記載の使用。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09290710A EP2298831B1 (de) | 2009-09-17 | 2009-09-17 | Schaumarme Netzmittel |
EP09290710.4 | 2009-09-17 | ||
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 (ja) | 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 (ja) |
EP (1) | EP2298831B1 (ja) |
JP (1) | JP5657004B2 (ja) |
CN (1) | CN102498154B (ja) |
BR (1) | BR112012005836A2 (ja) |
WO (1) | WO2011032664A2 (ja) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9559385B2 (en) * | 2013-02-06 | 2017-01-31 | Encell Technology, Inc. | Nickel iron battery employing an 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 |
CH505796A (de) * | 1967-04-03 | 1971-04-15 | Gen Aniline & Film Corp | Verfahren zur Herstellung von substituierten Carbamaten |
GB1402182A (en) * | 1972-04-10 | 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 |
AU2003244476A1 (en) * | 2002-02-07 | 2003-09-02 | Ucb, S.A. | Process using a cyclic carbonate reactant |
DE10257094A1 (de) * | 2002-12-05 | 2004-06-24 | Basf Ag | Enzymatische Herstellung urethangruppenhaltiger (Meth)acrylsäureester |
CN1723195A (zh) | 2002-12-12 | 2006-01-18 | 舒飞士特种化工有限公司 | 用于生产氨基甲酰氧基(甲基)丙烯酸酯的方法和新型的氨基甲酰氧基(甲基)丙烯酸酯 |
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 |
TW200512268A (en) * | 2003-07-18 | 2005-04-01 | Konishi Co Ltd | Curable resin composition and ambient temperature curable adhesive |
US20070197820A1 (en) | 2004-05-17 | 2007-08-23 | Jurgen Van Holen | Process for producing urethane (meth)acrylates and new urethane (meth)acrylates |
-
2009
- 2009-09-17 EP EP09290710A patent/EP2298831B1/de active Active
-
2010
- 2010-09-09 CN CN201080041278.3A patent/CN102498154B/zh active Active
- 2010-09-09 WO PCT/EP2010/005554 patent/WO2011032664A2/de active Application Filing
- 2010-09-09 JP JP2012529143A patent/JP5657004B2/ja not_active Expired - Fee Related
- 2010-09-09 US US13/395,968 patent/US8629297B2/en active Active
- 2010-09-09 BR BR112012005836A patent/BR112012005836A2/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
WO2011032664A2 (de) | 2011-03-24 |
JP2013505306A (ja) | 2013-02-14 |
EP2298831B1 (de) | 2013-02-20 |
EP2298831A1 (de) | 2011-03-23 |
CN102498154B (zh) | 2014-04-16 |
WO2011032664A3 (de) | 2011-09-15 |
US8629297B2 (en) | 2014-01-14 |
CN102498154A (zh) | 2012-06-13 |
US20120172618A1 (en) | 2012-07-05 |
BR112012005836A2 (pt) | 2017-09-12 |
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