ES2202881T3 - Microemulsiones acuosas. - Google Patents

Microemulsiones acuosas.

Info

Publication number: ES2202881T3
Authority: ES; Spain
Prior art keywords: esters; microemulsion; members; group; functionalized
Prior art date: 1997-07-31
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 - Lifetime

Application number

ES98938097T

Other languages

English (en)

Spanish (es)

Inventor

Eric W. Kaler

Timothy Donald Krizan

Larry D. Ryan

Martin Swanson Vethamuthu

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

University of Delaware

EIDP Inc

Original Assignee

University of Delaware

EI Du Pont de Nemours and Co

Priority date (The priority date 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 date listed.)

1997-07-31

Filing date

1998-07-30

Publication date

2004-04-01

1998-03-30 Priority claimed from US09/050,307 external-priority patent/US6165962A/en

1998-07-30 Application filed by University of Delaware, EI Du Pont de Nemours and Co filed Critical University of Delaware

2004-04-01 Application granted granted Critical

2004-04-01 Publication of ES2202881T3 publication Critical patent/ES2202881T3/es

2018-07-30 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000004530 micro-emulsion Substances 0.000 title claims abstract description 125
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 59
239000004094 surface-active agent Substances 0.000 claims abstract description 46
229930195733 hydrocarbon Natural products 0.000 claims abstract description 43
150000002430 hydrocarbons Chemical class 0.000 claims abstract description 43
150000002148 esters Chemical class 0.000 claims abstract description 36
239000004215 Carbon black (E152) Substances 0.000 claims abstract description 35
150000002009 diols Chemical class 0.000 claims abstract description 33
-1 tetraesters Chemical class 0.000 claims abstract description 21
150000001242 acetic acid derivatives Chemical class 0.000 claims abstract description 9
150000002596 lactones Chemical class 0.000 claims abstract description 8
125000000129 anionic group Chemical group 0.000 claims abstract description 6
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims abstract description 5
150000005690 diesters Chemical class 0.000 claims abstract description 5
150000005691 triesters Chemical class 0.000 claims abstract description 5
239000000203 mixture Substances 0.000 claims description 87
238000004140 cleaning Methods 0.000 claims description 29
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims description 20
239000002904 solvent Substances 0.000 claims description 18
239000003960 organic solvent Substances 0.000 claims description 17
239000002562 thickening agent Substances 0.000 claims description 14
150000001298 alcohols Chemical class 0.000 claims description 13
XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims description 11
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 11
229940015975 1,2-hexanediol Drugs 0.000 claims description 10
150000001279 adipic acids Chemical class 0.000 claims description 10
FBELJLCOAHMRJK-UHFFFAOYSA-L disodium;2,2-bis(2-ethylhexyl)-3-sulfobutanedioate Chemical group [Na+].[Na+].CCCCC(CC)CC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CC(CC)CCCC FBELJLCOAHMRJK-UHFFFAOYSA-L 0.000 claims description 10
FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 claims description 10
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 10
QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 claims description 9
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 9
239000003795 chemical substances by application Substances 0.000 claims description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
150000004996 alkyl benzenes Chemical class 0.000 claims description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
RJLKIAGOYBARJG-UHFFFAOYSA-N 1,3-dimethylpiperidin-2-one Chemical compound CC1CCCN(C)C1=O RJLKIAGOYBARJG-UHFFFAOYSA-N 0.000 claims description 5
125000002091 cationic group Chemical group 0.000 claims description 5
150000002311 glutaric acids Chemical class 0.000 claims description 5
235000011044 succinic acid Nutrition 0.000 claims description 5
150000003444 succinic acids Chemical class 0.000 claims description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
229920002125 Sokalan® Polymers 0.000 claims description 4
239000002253 acid Substances 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
150000001875 compounds Chemical class 0.000 claims description 4
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical class CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 claims description 4
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
150000002576 ketones Chemical class 0.000 claims description 4
229920000642 polymer Polymers 0.000 claims description 4
RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 4
150000007513 acids Chemical class 0.000 claims description 3
BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 claims description 3
229920003086 cellulose ether Polymers 0.000 claims description 3
150000005676 cyclic carbonates Chemical class 0.000 claims description 3
239000004584 polyacrylic acid Substances 0.000 claims description 3
229920002635 polyurethane Polymers 0.000 claims description 3
239000004814 polyurethane Substances 0.000 claims description 3
150000003462 sulfoxides Chemical class 0.000 claims description 3
150000003505 terpenes Chemical class 0.000 claims description 3
235000007586 terpenes Nutrition 0.000 claims description 3
HNSDLXPSAYFUHK-UHFFFAOYSA-N 1,4-bis(2-ethylhexyl) sulfosuccinate Chemical class CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC HNSDLXPSAYFUHK-UHFFFAOYSA-N 0.000 claims description 2
CLJDUFMUISGSEC-UHFFFAOYSA-N 1,4-bis(4-methylpentan-2-yloxy)-1,4-dioxobutane-2-sulfonic acid Chemical class CC(C)CC(C)OC(=O)CC(S(O)(=O)=O)C(=O)OC(C)CC(C)C CLJDUFMUISGSEC-UHFFFAOYSA-N 0.000 claims description 2
CBCQTCPKFYFJEU-UHFFFAOYSA-N 1,4-dioxo-1,4-dipentoxybutane-2-sulfonic acid Chemical class CCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCC CBCQTCPKFYFJEU-UHFFFAOYSA-N 0.000 claims description 2
MHIBEGOZTWERHF-UHFFFAOYSA-N heptane-1,1-diol Chemical class CCCCCCC(O)O MHIBEGOZTWERHF-UHFFFAOYSA-N 0.000 claims description 2
WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 claims description 2
235000011037 adipic acid Nutrition 0.000 claims 5
150000004945 aromatic hydrocarbons Chemical class 0.000 claims 2
125000000545 (4R)-limonene group Chemical group 0.000 claims 1
150000003950 cyclic amides Chemical class 0.000 claims 1
159000000000 sodium salts Chemical class 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
239000000839 emulsion Substances 0.000 description 13
238000009472 formulation Methods 0.000 description 13
239000003973 paint Substances 0.000 description 12
XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical group COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 10
239000003921 oil Substances 0.000 description 10
125000003118 aryl group Chemical group 0.000 description 7
238000000034 method Methods 0.000 description 7
238000002156 mixing Methods 0.000 description 7
239000010410 layer Substances 0.000 description 6
UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 5
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 5
238000003756 stirring Methods 0.000 description 5
239000000654 additive Substances 0.000 description 4
239000004519 grease Substances 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000000126 substance Substances 0.000 description 4
MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
238000005481 NMR spectroscopy Methods 0.000 description 3
238000007792 addition Methods 0.000 description 3
238000005238 degreasing Methods 0.000 description 3
239000002184 metal Substances 0.000 description 3
238000010587 phase diagram Methods 0.000 description 3
ONBWNNUYXGJKKD-UHFFFAOYSA-N 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonic acid;sodium Chemical compound [Na].CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC ONBWNNUYXGJKKD-UHFFFAOYSA-N 0.000 description 2
XHEDTHUFPRAWPH-UHFFFAOYSA-N 1,4-bis(4-methylpentan-2-yloxy)-1,4-dioxobutane-2-sulfonic acid;sodium Chemical compound [Na].CC(C)CC(C)OC(=O)CC(S(O)(=O)=O)C(=O)OC(C)CC(C)C XHEDTHUFPRAWPH-UHFFFAOYSA-N 0.000 description 2
CDFWDLTWTVIPBT-UHFFFAOYSA-N 1,4-dioxo-1,4-dipentoxybutane-2-sulfonic acid;sodium Chemical compound [Na].CCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCC CDFWDLTWTVIPBT-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 2
238000000149 argon plasma sintering Methods 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000013527 degreasing agent Substances 0.000 description 2
FSCIDASGDAWVED-UHFFFAOYSA-N dimethyl hexanedioate;dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC.COC(=O)CCCCC(=O)OC FSCIDASGDAWVED-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical group CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
229940051250 hexylene glycol Drugs 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000007654 immersion Methods 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
239000000693 micelle Substances 0.000 description 2
239000011368 organic material Substances 0.000 description 2
238000005191 phase separation Methods 0.000 description 2
BTJYKXPSPBJJDQ-UHFFFAOYSA-M sodium;1,4-bis(4-methylpentan-2-yloxy)-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].CC(C)CC(C)OC(=O)CC(S([O-])(=O)=O)C(=O)OC(C)CC(C)C BTJYKXPSPBJJDQ-UHFFFAOYSA-M 0.000 description 2
238000010998 test method Methods 0.000 description 2
RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 2
229940099259 vaseline Drugs 0.000 description 2
DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 1
229940031723 1,2-octanediol Drugs 0.000 description 1
UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 1
RVHOBHMAPRVOLO-UHFFFAOYSA-N 2-ethylbutanedioic acid Chemical compound CCC(C(O)=O)CC(O)=O RVHOBHMAPRVOLO-UHFFFAOYSA-N 0.000 description 1
241001454395 Alvania Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
UWIULCYKVGIOPW-UHFFFAOYSA-N Glycolone Natural products CCOC1=C(CC=CC)C(=O)N(C)c2c(O)cccc12 UWIULCYKVGIOPW-UHFFFAOYSA-N 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
206010061218 Inflammation Diseases 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
235000011613 Pinus brutia Nutrition 0.000 description 1
241000018646 Pinus brutia Species 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
238000000333 X-ray scattering Methods 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
238000013019 agitation Methods 0.000 description 1
230000002051 biphasic effect Effects 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
239000011247 coating layer Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000010276 construction Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
BNMYXGKEMMVHOX-UHFFFAOYSA-N dimethyl butanedioate;dimethyl pentanedioate Chemical compound COC(=O)CCC(=O)OC.COC(=O)CCCC(=O)OC BNMYXGKEMMVHOX-UHFFFAOYSA-N 0.000 description 1
OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
238000002296 dynamic light scattering Methods 0.000 description 1
239000003623 enhancer Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000011152 fibreglass Substances 0.000 description 1
230000000415 inactivating effect Effects 0.000 description 1
230000004054 inflammatory process Effects 0.000 description 1
238000011835 investigation Methods 0.000 description 1
238000003475 lamination Methods 0.000 description 1
229940094522 laponite Drugs 0.000 description 1
XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
235000012243 magnesium silicates Nutrition 0.000 description 1
238000003760 magnetic stirring Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 description 1
238000010422 painting Methods 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000006748 scratching Methods 0.000 description 1
230000002393 scratching effect Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000001998 small-angle neutron scattering Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
UMEWSJNRBXKWKZ-UHFFFAOYSA-M sodium;1,4-dioxo-1,4-dipentoxybutane-2-sulfonate Chemical compound [Na+].CCCCCOC(=O)CC(S([O-])(=O)=O)C(=O)OCCCCC UMEWSJNRBXKWKZ-UHFFFAOYSA-M 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/43—Solvents
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/123—Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0017—Multi-phase liquid compositions
- C11D17/0021—Aqueous microemulsions
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2044—Dihydric alcohols linear
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2048—Dihydric alcohols branched

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Detergent Compositions (AREA)
Cosmetics (AREA)
Colloid Chemistry (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)

ES98938097T 1997-07-31 1998-07-30 Microemulsiones acuosas. Expired - Lifetime ES2202881T3 (es)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US90416697A	1997-07-31	1997-07-31
US904166		1997-07-31
US50307		1998-03-30
US09/050,307 US6165962A (en)	1997-07-31	1998-03-30	Aqueous microemulsions

Publications (1)

Publication Number	Publication Date
ES2202881T3 true ES2202881T3 (es)	2004-04-01

Family

ID=26728132

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES98938097T Expired - Lifetime ES2202881T3 (es)	1997-07-31	1998-07-30	Microemulsiones acuosas.

Country Status (10)

Country	Link
EP (1)	EP1000138B1 (da)
JP (1)	JP4271366B2 (da)
AT (1)	ATE250119T1 (da)
AU (1)	AU740364B2 (da)
BR (1)	BR9810847A (da)
DE (1)	DE69818271T2 (da)
DK (1)	DK1000138T3 (da)
ES (1)	ES2202881T3 (da)
PT (1)	PT1000138E (da)
WO (1)	WO1999006520A1 (da)

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JP4629354B2 (ja) *	2004-02-25	2011-02-09	三洋化成工業株式会社	界面活性剤組成物
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GB0605157D0 (en) *	2006-03-15	2006-04-26	Gramos Applied Ltd	Decontaminant formulations
JP5066881B2 (ja)	2006-09-27	2012-11-07	住友化学株式会社	乳剤組成物
EP2045320B1 (de) *	2007-09-19	2012-04-25	Bubbles & Beyond Gmbh	Reinigungsmittel zur Entfernung von Farbschichten von Oberflächen, Verfahren zur Herstellung des Mittels und Verfahren zur Reinigung
JP5256749B2 (ja)	2008-01-23	2013-08-07	住友化学株式会社	乳剤組成物
JP2009173578A (ja)	2008-01-24	2009-08-06	Sumitomo Chemical Co Ltd	乳剤組成物
JP5262131B2 (ja)	2008-01-24	2013-08-14	住友化学株式会社	乳剤組成物
DE102009013469B4 (de) *	2009-03-19	2014-04-17	Bubbles And Beyond Gmbh	Zubereitung zur äußerlichen Anwendung
DE102009014380A1 (de)	2009-03-26	2010-10-07	Bubbles And Beyond Gmbh	Verfahren und Zusammensetzung zum Reinigen von Gegenständen
CA2778222A1 (en) *	2009-10-19	2011-04-28	Rhodia Operations	Auto-emulsifying cleaning systems and methods for use
US9109191B2 (en)	2009-12-15	2015-08-18	Invista North America S.A.R.L.	Emulsion compositions and a method for selecting surfactants
WO2011081823A1 (en) *	2009-12-15	2011-07-07	Invista Technologies S.A.R.L.	Emulsion compositions and a method for selecting surfactants
EP2576748A4 (en) *	2010-06-02	2016-06-08	Rhodia Operations	USE OF ECO-FRIENDLY MICROEMULSIONS IN OIL CLEANING APPLICATIONS
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JP6199013B2 (ja) *	2012-07-19	2017-09-20	株式会社トクヤマＭｅｔｅｌ	洗浄剤及び洗浄方法
DE102018123858A1 (de) *	2018-09-27	2020-04-02	BÜFA GmbH & Co. KG	Lösungsmittel und Anwendung für ein Lösungsmittel
JP2024012062A (ja) *	2022-07-15	2024-01-25	荒川化学工業株式会社	洗浄剤及び洗浄方法

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1998
- 1998-07-30 AU AU86699/98A patent/AU740364B2/en not_active Ceased
- 1998-07-30 JP JP2000505264A patent/JP4271366B2/ja not_active Expired - Fee Related
- 1998-07-30 EP EP98938097A patent/EP1000138B1/en not_active Expired - Lifetime
- 1998-07-30 PT PT98938097T patent/PT1000138E/pt unknown
- 1998-07-30 DK DK98938097T patent/DK1000138T3/da active
- 1998-07-30 DE DE69818271T patent/DE69818271T2/de not_active Expired - Lifetime
- 1998-07-30 WO PCT/US1998/015744 patent/WO1999006520A1/en not_active Ceased
- 1998-07-30 ES ES98938097T patent/ES2202881T3/es not_active Expired - Lifetime
- 1998-07-30 AT AT98938097T patent/ATE250119T1/de active
- 1998-07-30 BR BR9810847-6A patent/BR9810847A/pt not_active IP Right Cessation

Also Published As

Publication number	Publication date
BR9810847A (pt)	2000-07-25
JP4271366B2 (ja)	2009-06-03
DK1000138T3 (da)	2004-02-02
DE69818271D1 (de)	2003-10-23
PT1000138E (pt)	2004-01-30
JP2002501087A (ja)	2002-01-15
AU740364B2 (en)	2001-11-01
DE69818271T2 (de)	2004-06-03
WO1999006520A1 (en)	1999-02-11
ATE250119T1 (de)	2003-10-15
EP1000138A1 (en)	2000-05-17
AU8669998A (en)	1999-02-22
EP1000138B1 (en)	2003-09-17

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US6165962A (en)	2000-12-26	Aqueous microemulsions
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TW209879B (da)	1993-07-21
US5171475A (en)	1992-12-15	Soil-removal microemulsion compositions
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