DE68901737T2 - Alkylsulphonylpercarbonsaeuren und die sie enthaltenden bleichmittel- und reinigungszusammensetzungen. - Google Patents

Alkylsulphonylpercarbonsaeuren und die sie enthaltenden bleichmittel- und reinigungszusammensetzungen.

Info

Publication number: DE68901737T2
Authority: DE; Germany
Prior art keywords: acid; bleaching; acids; bleaching agent; compound
Prior art date: 1988-03-21
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

Application number

DE1989601737

Other languages

German (de)

English (en)

Other versions

DE68901737D1 (de

Inventor

John Meijer

Den Berg Rolf Hendrik Van

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.)

Akzo Nobel NV

Original Assignee

Akzo NV

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.)

1988-03-21

Filing date

1989-03-16

Publication date

1993-02-04

1989-03-16 Application filed by Akzo NV filed Critical Akzo NV

1992-07-16 Application granted granted Critical

1992-07-16 Publication of DE68901737D1 publication Critical patent/DE68901737D1/de

1993-02-04 Publication of DE68901737T2 publication Critical patent/DE68901737T2/de

2009-03-17 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000002253 acid Substances 0.000 title claims description 36
150000007513 acids Chemical class 0.000 title claims description 19
239000000203 mixture Substances 0.000 title claims description 15
238000004140 cleaning Methods 0.000 title claims description 6
238000005422 blasting Methods 0.000 title 1
239000007844 bleaching agent Substances 0.000 claims description 34
238000004061 bleaching Methods 0.000 claims description 18
-1 n-octyl Chemical group 0.000 claims description 13
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 11
238000000034 method Methods 0.000 claims description 11
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 10
239000002243 precursor Substances 0.000 claims description 7
238000005406 washing Methods 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 5
229940098779 methanesulfonic acid Drugs 0.000 claims description 5
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
150000001735 carboxylic acids Chemical class 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 3
230000002378 acidificating effect Effects 0.000 claims description 2
238000006243 chemical reaction Methods 0.000 claims description 2
239000000645 desinfectant Substances 0.000 claims description 2
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 2
150000001875 compounds Chemical class 0.000 description 27
239000003599 detergent Substances 0.000 description 15
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 14
229910052760 oxygen Inorganic materials 0.000 description 14
239000001301 oxygen Substances 0.000 description 14
230000000694 effects Effects 0.000 description 12
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 10
JHUXOSATQXGREM-UHFFFAOYSA-N dodecanediperoxoic acid Chemical compound OOC(=O)CCCCCCCCCCC(=O)OO JHUXOSATQXGREM-UHFFFAOYSA-N 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
150000004965 peroxy acids Chemical class 0.000 description 7
238000003860 storage Methods 0.000 description 6
239000007795 chemical reaction product Substances 0.000 description 5
229940125782 compound 2 Drugs 0.000 description 5
238000009533 lab test Methods 0.000 description 5
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
239000004744 fabric Substances 0.000 description 4
235000008390 olive oil Nutrition 0.000 description 4
239000004006 olive oil Substances 0.000 description 4
239000004071 soot Substances 0.000 description 4
WQIPNMCAJJLXJU-UHFFFAOYSA-N 2-hexylsulfonylpropaneperoxoic acid Chemical compound CCCCCCS(=O)(=O)C(C)C(=O)OO WQIPNMCAJJLXJU-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
229920000742 Cotton Polymers 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
235000021028 berry Nutrition 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
230000000249 desinfective effect Effects 0.000 description 3
238000002156 mixing Methods 0.000 description 3
230000003287 optical effect Effects 0.000 description 3
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
235000020095 red wine Nutrition 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
239000004215 Carbon black (E152) Substances 0.000 description 2
229940126062 Compound A Drugs 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
239000012190 activator Substances 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
HDFRDWFLWVCOGP-UHFFFAOYSA-N carbonothioic O,S-acid Chemical compound OC(S)=O HDFRDWFLWVCOGP-UHFFFAOYSA-N 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
238000001914 filtration Methods 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
230000003301 hydrolyzing effect Effects 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
238000011065 in-situ storage Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000002002 slurry Substances 0.000 description 2
239000000344 soap Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
150000003457 sulfones Chemical class 0.000 description 2
QVCQPIJMAAOGKX-UHFFFAOYSA-N (2,4,5-trimethylphenyl)thiourea Chemical compound CC1=CC(C)=C(NC(N)=S)C=C1C QVCQPIJMAAOGKX-UHFFFAOYSA-N 0.000 description 1
238000005160 1H NMR spectroscopy Methods 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
HGJOCYGWJRYXCF-UHFFFAOYSA-N 2-decylsulfonylpropaneperoxoic acid Chemical compound CCCCCCCCCCS(=O)(=O)C(C)C(=O)OO HGJOCYGWJRYXCF-UHFFFAOYSA-N 0.000 description 1
NBTWATABDDLUAT-UHFFFAOYSA-N 2-decylsulfonylpropanoic acid Chemical compound CCCCCCCCCCS(=O)(=O)C(C)C(O)=O NBTWATABDDLUAT-UHFFFAOYSA-N 0.000 description 1
HHISOVLZPRJNGH-UHFFFAOYSA-N 2-hexylsulfonylpropanoic acid Chemical compound CCCCCCS(=O)(=O)C(C)C(O)=O HHISOVLZPRJNGH-UHFFFAOYSA-N 0.000 description 1
NBQPZFILNVSOPH-UHFFFAOYSA-N 2-nonylsulfonylpropanoic acid Chemical compound CCCCCCCCCS(=O)(=O)C(C)C(O)=O NBQPZFILNVSOPH-UHFFFAOYSA-N 0.000 description 1
JHKCYGGFYUKYEG-UHFFFAOYSA-N 2-octylsulfonylpropanoic acid Chemical compound CCCCCCCCS(=O)(=O)C(C)C(O)=O JHKCYGGFYUKYEG-UHFFFAOYSA-N 0.000 description 1
KRYOSDLLGJCUAY-UHFFFAOYSA-N 3-decylsulfonylpropaneperoxoic acid Chemical compound CCCCCCCCCCS(=O)(=O)CCC(=O)OO KRYOSDLLGJCUAY-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
JEPOHGAITDYLCI-UHFFFAOYSA-N C(CCCCCCCC)S(=O)(=O)C(C(=O)OO)C Chemical compound C(CCCCCCCC)S(=O)(=O)C(C(=O)OO)C JEPOHGAITDYLCI-UHFFFAOYSA-N 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
238000004566 IR spectroscopy Methods 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
KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
239000007832 Na2SO4 Substances 0.000 description 1
SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 description 1
239000004115 Sodium Silicate Substances 0.000 description 1
PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
244000269722 Thea sinensis Species 0.000 description 1
244000299461 Theobroma cacao Species 0.000 description 1
235000009470 Theobroma cacao Nutrition 0.000 description 1
125000005396 acrylic acid ester group Chemical group 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
230000002152 alkylating effect Effects 0.000 description 1
239000002280 amphoteric surfactant Substances 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
229940077388 benzenesulfonate Drugs 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000005282 brightening Methods 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
229930002875 chlorophyll Natural products 0.000 description 1
235000019804 chlorophyll Nutrition 0.000 description 1
ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
239000012459 cleaning agent Substances 0.000 description 1
229910052681 coesite Inorganic materials 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
229910052906 cristobalite Inorganic materials 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000005457 ice water Substances 0.000 description 1
238000011005 laboratory method Methods 0.000 description 1
239000006194 liquid suspension Substances 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
125000003136 n-heptyl 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])* 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
239000000047 product Substances 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000013042 solid detergent Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
235000021286 stilbenes Nutrition 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
229910052682 stishovite Inorganic materials 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
238000004448 titration Methods 0.000 description 1
229910052905 tridymite Inorganic materials 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
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3945—Organic per-compounds

Landscapes

Chemical & Material Sciences (AREA)
Inorganic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Detergent Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DE1989601737 1988-03-21 1989-03-16 Alkylsulphonylpercarbonsaeuren und die sie enthaltenden bleichmittel- und reinigungszusammensetzungen. Expired - Fee Related DE68901737T2 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP88200511		1988-03-21

Publications (2)

Publication Number	Publication Date
DE68901737D1 DE68901737D1 (de)	1992-07-16
DE68901737T2 true DE68901737T2 (de)	1993-02-04

Family

ID=8199765

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE1989601737 Expired - Fee Related DE68901737T2 (de)	1988-03-21	1989-03-16	Alkylsulphonylpercarbonsaeuren und die sie enthaltenden bleichmittel- und reinigungszusammensetzungen.

Country Status (6)

Country	Link
EP (1)	EP0334427B1 (es)
JP (1)	JPH01297499A (es)
DE (1)	DE68901737T2 (es)
DK (1)	DK134089A (es)
ES (1)	ES2042965T3 (es)
GR (1)	GR3005505T3 (es)

Families Citing this family (15)

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Publication number	Priority date	Publication date	Assignee	Title
US4758369A (en) *	1986-11-03	1988-07-19	Monsanto Company	Sulfone peroxycarboxylic acids
US5039447A (en) *	1988-12-12	1991-08-13	Monsanto Company	Pourable sulfone peracid compositions
CA2098353A1 (en) *	1992-06-15	1993-12-16	Yueting Chou	Sulfonamide peroxycarboxylic acids
DE19738442A1 (de) *	1997-09-03	1999-03-04	Siegfried Prof Dr Warwel	Perkohlensäurehalbester
US7939485B2 (en)	2004-11-01	2011-05-10	The Procter & Gamble Company	Benefit agent delivery system comprising ionic liquid
US20060090777A1 (en)	2004-11-01	2006-05-04	Hecht Stacie E	Multiphase cleaning compositions having ionic liquid phase
US7786065B2 (en) *	2005-02-18	2010-08-31	The Procter & Gamble Company	Ionic liquids derived from peracid anions
US8809392B2 (en)	2008-03-28	2014-08-19	Ecolab Usa Inc.	Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US8871807B2 (en)	2008-03-28	2014-10-28	Ecolab Usa Inc.	Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
BRPI0907918B1 (pt)	2008-03-28	2018-07-24	Ecolab Inc.	Ácidos sulfoperoxicarboxílicos, sua preparação e métodos de utilizção como agentes alvejantes e antimicrobianos
US9321664B2 (en)	2011-12-20	2016-04-26	Ecolab Usa Inc.	Stable percarboxylic acid compositions and uses thereof
US9926214B2 (en)	2012-03-30	2018-03-27	Ecolab Usa Inc.	Use of peracetic acid/hydrogen peroxide and peroxide-reducing agents for treatment of drilling fluids, frac fluids, flowback water and disposal water
US10165774B2 (en)	2013-03-05	2019-01-01	Ecolab Usa Inc.	Defoamer useful in a peracid composition with anionic surfactants
US8822719B1 (en)	2013-03-05	2014-09-02	Ecolab Usa Inc.	Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring
US20140256811A1 (en)	2013-03-05	2014-09-11	Ecolab Usa Inc.	Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8415909D0 (en) *	1984-06-21	1984-07-25	Procter & Gamble Ltd	Peracid compounds
ATE95812T1 (de) *	1986-11-03	1993-10-15	Monsanto Co	Sulfon-peroxycarbonsaeuren.

1989
- 1989-03-16 EP EP19890200656 patent/EP0334427B1/en not_active Expired
- 1989-03-16 DE DE1989601737 patent/DE68901737T2/de not_active Expired - Fee Related
- 1989-03-16 ES ES89200656T patent/ES2042965T3/es not_active Expired - Lifetime
- 1989-03-20 DK DK134089A patent/DK134089A/da not_active Application Discontinuation
- 1989-03-22 JP JP1067784A patent/JPH01297499A/ja active Pending
1992
- 1992-08-25 GR GR920401849T patent/GR3005505T3/el unknown

Also Published As

Publication number	Publication date
DK134089D0 (da)	1989-03-20
DK134089A (da)	1989-09-22
JPH01297499A (ja)	1989-11-30
DE68901737D1 (de)	1992-07-16
EP0334427B1 (en)	1992-06-10
GR3005505T3 (es)	1993-06-07
EP0334427A1 (en)	1989-09-27
ES2042965T3 (es)	1993-12-16

Legal Events

Date	Code	Title	Description
1993-07-08	8364	No opposition during term of opposition
1994-12-08	8327	Change in the person/name/address of the patent owner	Owner name: AKZO NOBEL N.V., ARNHEIM/ARNHEM, NL
1998-03-12	8339	Ceased/non-payment of the annual fee

Publication	Publication Date	Title
DE3886969T2 (de)	1994-04-28	Quartäre Ammonium- oder Phosphonium-Peroxycarbonsäure-Prekursoren und ihre Verwendung in Detergensbleichmittelzusammensetzungen.
DE3586957T2 (de)	1993-05-19	Persaeure- und bleichmittelaktivator-verbindungen und ihre verwendung in reinigungsmittelzusammensetzungen.
DE68901737T2 (de)	1993-02-04	Alkylsulphonylpercarbonsaeuren und die sie enthaltenden bleichmittel- und reinigungszusammensetzungen.
DE68908726T2 (de)	1993-12-23	Bleicher, die imidoaromatische Percarbonsäure enthalten.
DE69014384T2 (de)	1995-04-20	Bleichaktivierung.
DE68908439T2 (de)	1993-12-23	Quatenäre-Ammonium-Verbindungen zur Verwendung in Bleich-Systemen.
DE69019781T2 (de)	1995-11-09	Bleichmittelzusammensetzung.
DE68918561T2 (de)	1995-01-26	Bleichzusammensetzung.
DE3851177T2 (de)	1995-03-02	Salze von Perfettsäuren enthaltende Bleichmittel und derartige Zusammensetzungen und deren Vorstufen, die Amidgruppen in der Alkylgruppe haben.
DE3787784T2 (de)	1994-05-05	Sulfon-Peroxycarbonsäuren.
DE69122750T2 (de)	1997-05-07	Amidoperoxisäure enthaltende bleichkörnchen
DE69121563T2 (de)	1997-03-27	Vorläufer für die bleiche mit peroxysäure und reinigungsmittelzusammensetzungen die diese vorläufer enthalten
DE3245169A1 (de)	1983-06-16	Bleich- und waschmittelzusammensetzung
DE2530539C3 (de)	1981-11-05	Addukt aus Natriumsulfat, Wasserstoffperoxyd und Natriumchlorid und dessen Verwendung
EP0082823B1 (de)	1986-09-03	Verfahren zum Bleichen von Fasermaterialien unter Verwendung von Oligomeren von Phosphonsäureestern als Stabilisatoren in alkalischen, peroxydhaltigen Bleichflotten
DE2730246C2 (de)	1986-10-16	Mittel zum optischen Aufhellen von synthetischen oder natürlichen organischen Materialien und Verfahren zum Aufhellen von organischen textilen Materialien
DE68921051T2 (de)	1995-06-14	Pyridin-3-percarboxylsäure monopersulfat.
DE2000787C3 (de)	1974-10-03	2-n-Hydrocarbyl-butandiol-1,4-disulfate und diese enthaltende Wasch- und Reinigungsmittel
DE68904624T2 (de)	1993-06-03	Fluessige reinigungsmittelzusammensetzungen und verfahren zu deren herstellung.
DE1802017A1 (de)	1969-05-08	Bleich- und Waschmittel
EP0409846A1 (de)	1991-01-30	Aktivatoren für anorganische perverbindungen
DE2843127A1 (de)	1979-04-12	Verfahren zur entfernung von schmutz und/oder flecken aus stoffen
DE2242093C2 (de)	1982-02-25	Phosphatfreie alkyläthersulfathaltige Waschmittel
CH676007A5 (es)	1990-11-30
EP0427670A1 (de)	1991-05-15	Flüssigwaschmittel