CA2221982A1 - Composition chimique - Google Patents

Composition chimique Download PDF

Info

Publication number: CA2221982A1
Authority: CA; Canada
Prior art keywords: composition; acid; hydrogen; hydrogen peroxide; composition comprises
Prior art date: 1996-11-29
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.): Abandoned

Application number

CA002221982A

Other languages

English (en)

Inventor

Gunnil Jonsson

Gunilla Jadesjo

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.)

Nouryon Pulp and Performance Chemicals AB

Original Assignee

Eka Chemicals AB

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.)

1996-11-29

Filing date

1997-11-24

Publication date

1998-05-29

1997-11-24 Application filed by Eka Chemicals AB filed Critical Eka Chemicals AB

1998-05-29 Publication of CA2221982A1 publication Critical patent/CA2221982A1/fr

Status Abandoned legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 50
239000000126 substance Substances 0.000 title description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 65
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 36
239000004094 surface-active agent Substances 0.000 claims abstract description 17
239000008139 complexing agent Substances 0.000 claims abstract description 14
239000007864 aqueous solution Substances 0.000 claims abstract description 9
238000004061 bleaching Methods 0.000 claims abstract description 9
238000004659 sterilization and disinfection Methods 0.000 claims abstract description 9
238000004140 cleaning Methods 0.000 claims abstract description 8
235000008733 Citrus aurantifolia Nutrition 0.000 claims abstract description 7
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims abstract description 7
235000011941 Tilia x europaea Nutrition 0.000 claims abstract description 7
239000004571 lime Substances 0.000 claims abstract description 7
239000004753 textile Substances 0.000 claims abstract description 6
230000002378 acidificating effect Effects 0.000 claims abstract description 5
239000002253 acid Substances 0.000 claims description 23
WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 claims description 19
239000001257 hydrogen Substances 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 9
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
-1 piperidino, pyrrolidino Chemical group 0.000 claims description 8
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
150000001408 amides Chemical class 0.000 claims description 6
239000002736 nonionic surfactant Substances 0.000 claims description 6
150000003839 salts Chemical class 0.000 claims description 6
150000007513 acids Chemical class 0.000 claims description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
229910052783 alkali metal Inorganic materials 0.000 claims description 4
150000001340 alkali metals Chemical class 0.000 claims description 4
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
239000002280 amphoteric surfactant Substances 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
RXLKNGUPUSHCLQ-UHFFFAOYSA-N (dimethylamino)methyl-[hydroxy(methyl)phosphoryl]oxyphosphinic acid Chemical compound CN(C)CP(=O)(O)OP(=O)(O)C RXLKNGUPUSHCLQ-UHFFFAOYSA-N 0.000 claims description 2
239000003929 acidic solution Substances 0.000 claims description 2
125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
HMMPCBAWTWYFLR-UHFFFAOYSA-N n-pyridin-2-ylpyridin-2-amine Chemical compound C=1C=CC=NC=1NC1=CC=CC=N1 HMMPCBAWTWYFLR-UHFFFAOYSA-N 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
125000003884 phenylalkyl group Chemical group 0.000 claims description 2
PMWXGSWIOOVHEQ-UHFFFAOYSA-N pyridine-2,6-dicarbaldehyde Chemical compound O=CC1=CC=CC(C=O)=N1 PMWXGSWIOOVHEQ-UHFFFAOYSA-N 0.000 claims description 2
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 4
239000002738 chelating agent Substances 0.000 claims 2
SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims 2
RHZZEXPAZIBIPM-UHFFFAOYSA-N NCP(=O)(O)OP(=O)O Chemical compound NCP(=O)(O)OP(=O)O RHZZEXPAZIBIPM-UHFFFAOYSA-N 0.000 claims 1
229910019142 PO4 Inorganic materials 0.000 claims 1
KVUUQMDVROTSNI-UHFFFAOYSA-N [morpholin-4-yl(phosphono)methyl]phosphonic acid Chemical compound OP(O)(=O)C(P(O)(O)=O)N1CCOCC1 KVUUQMDVROTSNI-UHFFFAOYSA-N 0.000 claims 1
235000021317 phosphate Nutrition 0.000 claims 1
150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
229940081066 picolinic acid Drugs 0.000 claims 1
229960002163 hydrogen peroxide Drugs 0.000 description 29
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
IVHVNMLJNASKHW-UHFFFAOYSA-M Chlorphonium chloride Chemical compound [Cl-].CCCC[P+](CCCC)(CCCC)CC1=CC=C(Cl)C=C1Cl IVHVNMLJNASKHW-UHFFFAOYSA-M 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
238000005187 foaming Methods 0.000 description 4
150000007524 organic acids Chemical class 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
230000001580 bacterial effect Effects 0.000 description 3
239000003599 detergent Substances 0.000 description 3
230000007613 environmental effect Effects 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
150000002431 hydrogen Chemical class 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
102000004190 Enzymes Human genes 0.000 description 2
108090000790 Enzymes Proteins 0.000 description 2
210000004027 cell Anatomy 0.000 description 2
239000012459 cleaning agent Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
235000008504 concentrate Nutrition 0.000 description 2
XQRLCLUYWUNEEH-UHFFFAOYSA-N diphosphonic acid Chemical compound OP(=O)OP(O)=O XQRLCLUYWUNEEH-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000007800 oxidant agent Substances 0.000 description 2
150000003009 phosphonic acids Chemical class 0.000 description 2
239000000344 soap Substances 0.000 description 2
QYAPHLRPFNSDNH-MRFRVZCGSA-N (4s,4as,5as,6s,12ar)-7-chloro-4-(dimethylamino)-1,6,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide;hydrochloride Chemical compound Cl.C1=CC(Cl)=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]4(O)C(=O)C3=C(O)C2=C1O QYAPHLRPFNSDNH-MRFRVZCGSA-N 0.000 description 1
BSFODEXXVBBYOC-UHFFFAOYSA-N 8-[4-(dimethylamino)butan-2-ylamino]quinolin-6-ol Chemical compound C1=CN=C2C(NC(CCN(C)C)C)=CC(O)=CC2=C1 BSFODEXXVBBYOC-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241000195493 Cryptophyta Species 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
244000228957 Ferula foetida Species 0.000 description 1
YFONKFDEZLYQDH-OPQQBVKSSA-N N-[(1R,2S)-2,6-dimethyindan-1-yl]-6-[(1R)-1-fluoroethyl]-1,3,5-triazine-2,4-diamine Chemical compound C[C@@H](F)C1=NC(N)=NC(N[C@H]2C3=CC(C)=CC=C3C[C@@H]2C)=N1 YFONKFDEZLYQDH-OPQQBVKSSA-N 0.000 description 1
IKLMOINVJXOXGK-UHFFFAOYSA-N N1=C(C=CC=C1)C(=O)O.N1=C(C=CC=C1)C(=O)O.P(O)(O)=O Chemical compound N1=C(C=CC=C1)C(=O)O.N1=C(C=CC=C1)C(=O)O.P(O)(O)=O IKLMOINVJXOXGK-UHFFFAOYSA-N 0.000 description 1
241001648341 Orites Species 0.000 description 1
241000282320 Panthera leo Species 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
QHEQBPTYYOPKOT-UHFFFAOYSA-L [Na+].[Na+].P(=O)([O-])OP(=O)[O-].O1CCN(CC1)C Chemical compound [Na+].[Na+].P(=O)([O-])OP(=O)[O-].O1CCN(CC1)C QHEQBPTYYOPKOT-UHFFFAOYSA-L 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
210000000170 cell membrane Anatomy 0.000 description 1
239000013522 chelant Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000003086 colorant Substances 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
230000009918 complex formation Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
DKPHLYCEFBDQKM-UHFFFAOYSA-H hexapotassium;1-phosphonato-n,n-bis(phosphonatomethyl)methanamine Chemical compound [K+].[K+].[K+].[K+].[K+].[K+].[O-]P([O-])(=O)CN(CP([O-])([O-])=O)CP([O-])([O-])=O DKPHLYCEFBDQKM-UHFFFAOYSA-H 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
239000002563 ionic surfactant Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
229940099990 ogen Drugs 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
229960003903 oxygen Drugs 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000001243 protein synthesis Methods 0.000 description 1
239000013535 sea water Substances 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000000243 solution Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
230000014616 translation Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000002023 wood 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
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
- 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
- C11D1/88—Ampholytes; Electroneutral compounds
- 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
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2086—Hydroxy carboxylic acids-salts thereof
- 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
- C11D3/26—Organic compounds containing nitrogen
- C11D3/28—Heterocyclic compounds containing nitrogen in the ring
- 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
- C11D3/26—Organic compounds containing nitrogen
- C11D3/33—Amino carboxylic acids
- 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
- C11D3/36—Organic compounds containing phosphorus
- C11D3/361—Phosphonates, phosphinates or phosphonites
- 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
- C11D3/3947—Liquid compositions

Landscapes

Chemical & Material Sciences (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)
Inorganic Chemistry (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Detergent Compositions (AREA)

CA002221982A 1996-11-29 1997-11-24 Composition chimique Abandoned CA2221982A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
SE9604413A SE9604413D0 (sv)	1996-11-29	1996-11-29	Chemical composition
SE9604413-6		1996-11-29

Publications (1)

Publication Number	Publication Date
CA2221982A1 true CA2221982A1 (fr)	1998-05-29

Family

ID=20404814

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002221982A Abandoned CA2221982A1 (fr)	1996-11-29	1997-11-24	Composition chimique

Country Status (4)

Country	Link
EP (1)	EP0845526A3 (fr)
CA (1)	CA2221982A1 (fr)
NO (1)	NO975453L (fr)
SE (1)	SE9604413D0 (fr)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
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US6346279B1 (en)	1998-12-14	2002-02-12	Virox Technologies, Inc.	Hydrogen peroxide disinfectant with increased activity
EP1022327B1 (fr) *	1999-01-22	2006-04-05	The Procter & Gamble Company	Procédé pour le traitement de textiles en utilisant un additif pour la lessive
US6528471B1 (en)	1999-01-22	2003-03-04	The Procter & Gamble Company	Process of treating fabrics with a laundry additive
RU2167191C1 (ru) *	1999-11-12	2001-05-20	Парфенова Татьяна Аркадьевна	Многоцелевое жидкое моющее и очищающее средство
DE19961660A1 (de) *	1999-12-21	2001-07-12	Henkel Kgaa	Pflegemittel für Wasch- und Geschirrspülmaschinen
ATE289796T1 (de)	2001-01-16	2005-03-15	Unilever Nv	Orale zusammensetzung
WO2003067989A1 (fr)	2002-02-12	2003-08-21	Virox Technologies Inc.	Desinfectant au peroxyde d'hydrogene a activite amelioree
US7094430B2 (en)	2002-07-03	2006-08-22	Innovative Healthcare Products, Inc.	Antimicrobial solution for both tropical and oral use
US20080305182A1 (en)	2002-11-15	2008-12-11	Ramirez Jose A	Hydrogen peroxide disinfectant containing a cyclic carboxylic acid and/or aromatic alcohol
EP1562430B1 (fr)	2002-11-15	2009-08-05	Virox Technologies Inc.	Desinfectant a base de peroxyde d'hydrogene contenant un acide carboxylique cyclique et/ou un alcool aromatique
US7459005B2 (en)	2002-11-22	2008-12-02	Akzo Nobel N.V.	Chemical composition and method
RU2233924C1 (ru) *	2002-12-26	2004-08-10	Ивановский государственный химико-технологический университет	Состав для совмещенного способа беления и крашения целлюлозосодержащих текстильных материалов
US7470444B2 (en)	2006-04-28	2008-12-30	Delaval, Inc.	Tripe-bleaching composition
EP2225175B1 (fr)	2007-12-13	2012-12-12	Akzo Nobel N.V.	Solutions stabilisées de peroxyde d'hydrogène
US8871807B2 (en)	2008-03-28	2014-10-28	Ecolab Usa Inc.	Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
US8809392B2 (en)	2008-03-28	2014-08-19	Ecolab Usa Inc.	Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
NZ587218A (en)	2008-03-28	2012-04-27	Ecolab Inc	Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US12203056B2 (en)	2008-03-28	2025-01-21	Ecolab Usa Inc.	Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
EP2518759B1 (fr) *	2009-12-25	2017-06-21	Mitsubishi Gas Chemical Company, Inc.	Procédé de fabrication de dispositif à semi-conducteur utilisant un agent de gravure
US9321664B2 (en)	2011-12-20	2016-04-26	Ecolab Usa Inc.	Stable percarboxylic acid compositions and uses thereof
WO2013109671A1 (fr) *	2012-01-18	2013-07-25	The Procter & Gamble Company	Compositions détergentes acides pour lessive
EP2831000A4 (fr)	2012-03-30	2016-03-30	Ecolab Usa Inc	Utilisation de l'acide peracétique/peroxyde d'hydrogène et d'agents réducteurs de peroxyde pour le traitement des fluides de forage, des fluides frac, des eaux refoulées et des eaux usées
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
US10165774B2 (en)	2013-03-05	2019-01-01	Ecolab Usa Inc.	Defoamer useful in a peracid composition with anionic surfactants
RU2639433C2 (ru) *	2016-04-12	2017-12-21	Общество с ограниченной ответственностью "АНГАРА ДЕВЕЛОПМЕНТ", ООО "АНГАРА ДЕВЕЛОПМЕНТ"	Раствор для удаления отложений различной природы
US11428482B2 (en)	2016-04-12	2022-08-30	Angara Global Ltd.	Industrial cleaning systems, including solutions for removing various types of deposits, and cognitive cleaning
WO2018042353A1 (fr)	2016-08-30	2018-03-08	Church & Dwight Co., Inc.	Composition et procédé de désactivation d'allergènes
US10450535B2 (en)	2017-10-18	2019-10-22	Virox Technologies Inc.	Shelf-stable hydrogen peroxide antimicrobial compositions
EP3841059A1 (fr)	2018-08-22	2021-06-30	Ecolab USA Inc.	Stabilisation de peroxyde d'hydrogène et de peracide avec des molécules à base d'acide pyridine carboxylique en c -3, -4 ou -5
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1996
- 1996-11-29 SE SE9604413A patent/SE9604413D0/xx unknown
1997
- 1997-11-05 EP EP97203428A patent/EP0845526A3/fr not_active Withdrawn
- 1997-11-24 CA CA002221982A patent/CA2221982A1/fr not_active Abandoned
- 1997-11-27 NO NO975453A patent/NO975453L/no unknown

Also Published As

Publication number	Publication date
EP0845526A2 (fr)	1998-06-03
NO975453L (no)	1998-06-02
EP0845526A3 (fr)	1999-03-03
NO975453D0 (no)	1997-11-27
SE9604413D0 (sv)	1996-11-29

Legal Events

Date	Code	Title	Description
1997-11-24	EEER	Examination request
2000-11-24	FZDE	Discontinued

Publication	Publication Date	Title
CA2221982A1 (fr)	1998-05-29	Composition chimique
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