CA2221982A1 - Chemical composition - Google Patents
Chemical composition Download PDFInfo
- Publication number
- CA2221982A1 CA2221982A1 CA002221982A CA2221982A CA2221982A1 CA 2221982 A1 CA2221982 A1 CA 2221982A1 CA 002221982 A CA002221982 A CA 002221982A CA 2221982 A CA2221982 A CA 2221982A CA 2221982 A1 CA2221982 A1 CA 2221982A1
- Authority
- CA
- Canada
- Prior art keywords
- composition
- acid
- hydrogen
- hydrogen peroxide
- composition comprises
- 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.)
- Abandoned
Links
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
Abstract
The invention relates to a composition suitable for cleaning, disinfection and bleaching comprising an acidic aqueous solution of hydrogen peroxide, a surfactant, a phosphonic acid based complexing agent and citric acid. The invention also relates to use of such a composition for disinfection, bleaching, removal of stains from textiles, or removal of lime deposits.
Description
CHEMICAL COMPOSITION
The preserlt invention relates to an acidic aqueous composilion suitable for cleaning, disi"fection and/or bleaching cor"priai"g hydrogen peroxide, as well as use of such a co,nposition.
Hard surface cleaning and disi"re~,1ion, laundry bleaching and stain-removal, doi"e~lic as well as industrial, is often pe,rur,,,ed with ch!ari"e based che"~icals such as hy~,och'Drite in aqueous solution which generally is effective for disi"re~;tion and bleach-ing, or organic solvents, enzymes and surfactants effective for stain-removal. However, hy~Gch'orite is not useful for removing lime soap and it may also damage textile fibres 10 and the original colours thereof. Further, for environmental reasons it is desi, ~'e to avoid chlorine based cleaning agents.
Hydrogen peroxide is known as an env;ronmerilal friendly oxidiser and disinfec-tant, but to be effficient a rather high concerlt,alion and/or a long contact time is neces-sary. In the bacterial cell hydrogen peroxide reacts with -SH groups and thereby destroys 15 SH containing enzymes and inhibit the protein synthesis. However, hydrogen peroxide has a poor storage stability, particularly in comb-.,dlion with other ingredients such as su,rdctants or organic acid. Although the hydrogen peroxide stability can be improved by addition of cheldlil,g agents like phosphondles, it is hard to find a phosphonate that both is biodegradable and effective as a hydrogen peroxide sl~ ,er.
EP-B1-87049 cliscloses a composition for disinfection co",prisi"g hydrogen per-oxide, an acidic phosphorous compound such as phosphoric acid, and a complexing agent selected from certain phosphonic acids or salts thereof.
EP-A1 -517996 ~isclQses a hydrogen peruxide based bleaching composition col"p,ising a specific class of surfactants.
WPI Acc. No 93-004727/01, abstract of JP-A- 4332800 discloses a detergent composition col"p,i~ing hydrogen peroxide, an organic or inorganic acid, and a carbox-ylic acid type polymer.
WPI Acc. No 88-004846/01, abstract of JP-A-62270509 discloses a composition for removing marine creatures from constructions used in sea water, the co",posilion 30 compl ising citric acid, hydrogen peroxide and a surfactant.
WO 93/14183 ~iscl~ses a detergeril composition col"prisi"g a surfactant, oxy-gen bleach such as hydrogen peroxide and a metal sequestering agent.
WO 91/08981 ~isclQses a solution for stabili~ g hydrogen peroxide COI"p,isi"9 citric acid, tartaric acid and phosphoric acid.
WO 94/07803 discloses the use of a composition co",prisi"g an oxidising agent an organic acid and a phosphonic acid for removing magnetite deposits in water supply systems.
It is an object of the present invention to provide a storage stable composition5 based on hydrogen peroxide which is effective for several functions including cleaning ble-~hing disinfection removal of stains on textiles and removal of lime deposita. It is another object of the invention to provide a co",position only containing envi,onmentally acceptable co",ponentà. The col"positiGn according to the invention comprises an acidic aqueous solution of hydrogen peruxide a surfactant citric acid and a complexing agent 10 based on phosphonic acid dipicolinic acid or derivatives thereof. Suitably the pH of the composition is below 4 preferdbly below 3 most prererdbly below 2 which improves the ar,li",icrobial activity as well as the capability of removing lime deposits or lime soap in for example bath tubs toilet bowls or the like. A low pH also improves the stability of the hydrogen peroxide. However the pH preferably is above about 0.5 most preferably 15 above about 1.
It has SUI~ riai,,yly been found that citric acid unlike most environmental friendly acids does not cause any subslantial decomposilion of the hydrogen peroxide in aque-ous co""~ositions also containing surfactants and phosphon.c acid or dipicolinic acid based complexing agents. It is prefel,ed that apart from citric acid and phosphonic 20 and/or dipicolinic acids or derivatives thereof the co",posilion does not contain any sub-stantial amounts of other organic acids. From an environmental point of view it is also prerel,~d that the composition does not cor"prise any subaldnlial amounts of phosphoric acid or phosphales.
The surfactant facilitates removal of dirt and especially non-ionic surfactants are 25 excellent on removing fat and pigments but they also enhance the ar,li",icrobial effect as they destroy bacterial cell membranes. Preferred surfactants are compatible with hydro-gen peroxide in acidic solutions which means that neither do they cause decomposilion of the hydrogen peroxide nor does the hydrogen peroxide or the acid cause decomposi-tion of the surfactants. Further the surfactants are preferably env;,oh,nenlal friendly and 30 biodegradable.
The co,nposition contains one or several different surfactants. P~eferably it comprises a non-ionic surfactant or an ar"photelic surfactant or a mixture thereof. Al-though not preferred it is also possible to include an-ionic surfactants as an alternative or as a complement.
Plefelled non-ionic surfactants are selected from ethoxylated fatty acids alco-hols amines or amides prefer~bly comprising from 1 to 12 most preferdbly from 4 to 8 mols ethylene oxide per mol acid, alcohol, amine or amide. r~ eferably the acid, alcohol or amide col"p,ises from 7 to 15, most preferably from 9 to 11 carbon atoms. Useful non-ionic surfactants can be high foaming such as an ethoxylated alcohol contai"L,g 11 car-bon atoms and 8 ethylene oxides, or low foaming such as a narrow range ethoxylated 5 alcohol containing 9 carbon atoms and 6 ethylene oxides.
P,ere"ed amphoteric sl"ractanta are selected from derivatives of preferably ali-phatic amines comprising one or more anionic groups such as carboxy, sulfo, or sulfato.
Particularly prefer,ed amphoteric surfactants satisfy the formula:
(CH2)X-COOM
(CH2)~R' 15 wherein x and y are, independently from each other, from 1 to 5, R' is -COOM2 or -OH, M~ and M2 are, i"depender,lly from each other, H, ammonium or an alkali metal such as Na, K or Li, R is a straight or a branched carbon chain having from 1 to 8 carbon atoms or an amide of the formula:
O H
Il I
Rn-C-N-wherein R" is a straight or a brdnched carbon chain having from 1 to 8 carbon atoms. It is pref~r,ed that R' is COOM2 and that R is a straight or a branched carbon chain. Exam-ples of prerer,ed a""~hote,ic surfactants are octylimino di~rop onate and capryloampho ~:~cet~le which are commercially available under the trademarks Ampholak~) YJH40(Akzo Nobel) and Ampholakg) XJO (Akzo Nobel), respectively.
At least one complexing agent based on phosphonic acid, dipicolinic acid or de-rivatives thereof should be included in order to obtain satisfactory storage stability of the hydrogen peroxide. One or several phosphonic acid based complexing agents is pref-erably present in an amount from about 0.5 wt% to about 10 wt%, most preferably from about 1 wt% to about 4 wt% based on the content of hydrogen peroxide. Dipicolinic acid or derivatives thereof may be present in an amount from about 0.25 to about 5 wt%, preferably from about 0.5 to about 2 wt% based on the content of hydrogen peroxide.
The complexing agents also enhance the microbial effect since they chelate cat-ions like ",ag"esium and calcium which have an important role in the bacterial cell. Examples of useful derivatives of dipicolinic acid are picGl;.l c acid, acid, 2,6-pyridine dialdehyde or CA 0222l982 l997-ll-24 2,2-dipyridyl amine. Examples of useful phosphon c acid based compl xing agents are those that are com"~eru;ally available such as 1-hydroxyethylidene-1,1-diphosphon c acid, 1-amifio~tl,ane-1,1-diphosphonic acid, aminotri (methylanephosphon--c acid), ethylene diamine tetra (methyle,)ephosphon-c acid), hexar"etl ,ylene diar"ine tetra 5 (methylenephosphonic acid), diethylanel,ia"tine penta (methylenephosphon.c acid) and diethylenet,iar,line hexa (methylenephosphon c acid), as well as salts thereof. Particularly high stability can be ach-.eved by including both a phosphon.c acid and dipicolinic acid or a derivative thereof.
Preferred phosphon-~ acid based complexing agents are those that are at least 10 partly biodegradable. Thert:fore, the composition pleferably cGillp~ises a complexing agent sEle~1ed from biodegradable 1-aminoalkane-1,1-diphosphonic acids, or salts thereof, pr~fei dbly of the formula:
OX, R~ OX3 O=P--Cl--IP=O
wherein R~ is selected from hydrogen, C1-C4 alkyl and phenyl; R2 and R3, independently from each other, are selected from hydrogen, C~-C22 alkyl, C5-C6 cycloalkyl, phenyl, C7-C~8 alkylphenyl, C7-C,8 phenylalkyl, a C~-C~0 alkanol radical, a carboxy alkyl radical hav-ing up to 10 carbon atoms, wherein R2 and R3 together with the nitrogen atom can form a piperidino, pyrrolidino or a morpholino group; and X~ to X4, independently from each other, are selected from hydrogen, alkali metal and ammonium. Preparation of such phosphonic acids are described in, for example, US 3899496, US 3979385 and nSynthesis of 1-dialkylaminoalkylidene diphosphonic acids and their properties for com-plex formation", Fukuda, M., et al, Yukagaku, Vol. 25, No. 6, pp. 362-64 (1976).Preferably R~ is hydrogen. It is also prefer,dd that R2 and R3 are selected fromhydrogen, C~ to C4 alkyl, or together with the r,it,ugen form a morpholino group. Particu-larly preferred co",F'exing agent are selected from r"or,uholino"~ ane diphosphonic acid, N,N-dimethyl aminodimethyl diphosphonic acid, aminomethyl diphosphon-c acid, or salts thereof, pr~rerably sodium salts.
A composition of the invention can be in the form of a concent,ale intended to be diluted before use. Such a concentrate may suitably contain from about 10 wt% to about 60 wt%, preferably from about 30 wt% to about 50 wt% of hydrogen peroxide, from about 5 wt% to about 30 wt%, prt:r~rdbly from about 10 wt% to about 20 wt% of surfac-tants, from about 0.5 wt% to about 10 wt% pr~fer~bly from about 1 wt% to about 5 wt%
of citric acid, and from about 0.05 wt% to about 10 wt%, prererably from about 1 wt% to about 5 wt% of phosphon e acid based complexing agents, alternatively from about 0.025 to about 5 wt%, p,t:~erably from about 0.5 to about 2.5 wt% of dipicolinic acid or deriva-5 tives thereof. The balance is preferably mainly made up of water. The pH of the concen-trate is suitably from about 0.5 to about 3, preferably from about 1 to about 2. Such a composition is prere~bly diluted from about 10 to about 50 times before use and is then particularly suitable for cleaning and disinfection of hard surfaces, particularly in the food industry where it is i",poilant to destroy human pdll,ogen c as well as product spoiling 10 micro-oryanisills and spores.
A ready to use composition suit-~'e for cleaning, disinfection or stain removal in households suitably contains from about 0.1 wt% to about 10 wt%, preferably from about 4 wt% to about 6 wt% of hydrogen peroxide, from about 0.1 wt% to about 10 wt%, pref-erably from about 2 wt% to about 6 wt% of surfactants, from about 0.1 wt% to about 3 15 wt% preferably from about 0.5 wt% to about 1 wt% of citric acid, and from about 0.01 wt% to about 5 wt%, ple:ferdbly from about 0.1 wt% to about 1 wt% of phosphonic acid based cGi"p'exing agents, alternatively from about 0.005 to about 2.5 wt%, preferably from about 0.05 to about 0.5 wt% of dipicolinic acid or derivatives thereof. The balance is preferably mainly made up of water. The pH of the composition is suitably from about 1 20 to about 4, preferdbly from about 2 to about 3. The composition is very effective for cleaning hard surfaces in kilchens and bathrooms and for removing stains from textiles. It can also be used outdoors for removing or inhibiting growth of mould or algae on wood or other materials. If appropridle, it can be cor"~..,ed with other cleaning agents or deter-gents, such as ordinary alkaline detergents for machine washing.
A composition of the invention can easily be prepared by simply mixing the components to desired concent,;~lions.
The invention also relates to use of a composition as described herein for disin-fection, bleaching, removal of stains from textiles, or removal of lime deposits.
The invention is further illustrated through the following examples which, how-ever, are not intended to limit the scope of the invention. If not otherwise stated, all con-tents and percentages refer to % by weight.
FY~rnple 1: A cG",position according to the invention consisting of an aqueous solution of 5% of hydrogen peroxide, 5% of ethoxylated C~0-C14 fatty alcohols with 7 mols ethylene oxide and 1 mol propylene oxide as a high foai"ing non-ionic surrdctanl, 0.2%
of morpholino",~tl,ane diphosphonic acid disodium salt and 1% of citric acid was pre-pared by mixing the components. The pH was 2.3. The stability of the hydrogen peroxide CA 0222l982 l997-ll-24 was tested by storing the composition 42 days at 40~C. It was found that 95.9% of the hydrogen peroxide remained.
FY~mple ~- A composi~ion according to the invention consisli,lg of an aqueous solution of 5% of hydrogen peroxide, 2.5% of ethoxylated C10-c14 fatty alcohols with 7 5 mols ethylene oxide and 1 mol propylene oxide as a high foaming non-ionic sulrd~tanl, 2.5% of ethoxylated C~6-C~8 amide with 4 mols ethylene oxide as a low roaming non-ionic su,raulanl, 0.2% of mor,uholino",ethane diphosphonic acid disodium salt and 1% of citric acid was prepared by mixing the co",ponenls. The pH was 2.5. The stability of hydrogen peroxid was tested by storing the composition 42 days at 40~C. It was found that 96.6%
10 of the hydlugen peroxide remained.
FY:3rnple 3: A composilion A according to the invention consi~li,lg of an aqueous solution of 4.9% of hydrogen peroxide, 50 g/l of ethoxylated C10-C14 fatty alcohols with 7 mols ethylene oxide and 1 mol propylene oxide as a high foaming non-ionic surfactant, 2 9/l of morpholinomethane diphosphonic acid disodium salt and 10 g/l of citric acid was 15 prepared by mixing the components. The pH was 2.3. A composition B accordi,lg to the invention was prepared in the same way with the exception that 1-hydroxyethylidene-1,1-diphosphon ~ acid was used instead of mor,uhG'i.lomethane diphosphonic acid which gave a pH of 1.8 The stability of the hydrogen peroxide was tested by storing the compositions 830 days at room temperature (about 20-25~C. It was found that the hydrogen peroxide 20 conce, Itldtion after storage was 3.9% in composition A and 2.9% in composition B.
The preserlt invention relates to an acidic aqueous composilion suitable for cleaning, disi"fection and/or bleaching cor"priai"g hydrogen peroxide, as well as use of such a co,nposition.
Hard surface cleaning and disi"re~,1ion, laundry bleaching and stain-removal, doi"e~lic as well as industrial, is often pe,rur,,,ed with ch!ari"e based che"~icals such as hy~,och'Drite in aqueous solution which generally is effective for disi"re~;tion and bleach-ing, or organic solvents, enzymes and surfactants effective for stain-removal. However, hy~Gch'orite is not useful for removing lime soap and it may also damage textile fibres 10 and the original colours thereof. Further, for environmental reasons it is desi, ~'e to avoid chlorine based cleaning agents.
Hydrogen peroxide is known as an env;ronmerilal friendly oxidiser and disinfec-tant, but to be effficient a rather high concerlt,alion and/or a long contact time is neces-sary. In the bacterial cell hydrogen peroxide reacts with -SH groups and thereby destroys 15 SH containing enzymes and inhibit the protein synthesis. However, hydrogen peroxide has a poor storage stability, particularly in comb-.,dlion with other ingredients such as su,rdctants or organic acid. Although the hydrogen peroxide stability can be improved by addition of cheldlil,g agents like phosphondles, it is hard to find a phosphonate that both is biodegradable and effective as a hydrogen peroxide sl~ ,er.
EP-B1-87049 cliscloses a composition for disinfection co",prisi"g hydrogen per-oxide, an acidic phosphorous compound such as phosphoric acid, and a complexing agent selected from certain phosphonic acids or salts thereof.
EP-A1 -517996 ~isclQses a hydrogen peruxide based bleaching composition col"p,ising a specific class of surfactants.
WPI Acc. No 93-004727/01, abstract of JP-A- 4332800 discloses a detergent composition col"p,i~ing hydrogen peroxide, an organic or inorganic acid, and a carbox-ylic acid type polymer.
WPI Acc. No 88-004846/01, abstract of JP-A-62270509 discloses a composition for removing marine creatures from constructions used in sea water, the co",posilion 30 compl ising citric acid, hydrogen peroxide and a surfactant.
WO 93/14183 ~iscl~ses a detergeril composition col"prisi"g a surfactant, oxy-gen bleach such as hydrogen peroxide and a metal sequestering agent.
WO 91/08981 ~isclQses a solution for stabili~ g hydrogen peroxide COI"p,isi"9 citric acid, tartaric acid and phosphoric acid.
WO 94/07803 discloses the use of a composition co",prisi"g an oxidising agent an organic acid and a phosphonic acid for removing magnetite deposits in water supply systems.
It is an object of the present invention to provide a storage stable composition5 based on hydrogen peroxide which is effective for several functions including cleaning ble-~hing disinfection removal of stains on textiles and removal of lime deposita. It is another object of the invention to provide a co",position only containing envi,onmentally acceptable co",ponentà. The col"positiGn according to the invention comprises an acidic aqueous solution of hydrogen peruxide a surfactant citric acid and a complexing agent 10 based on phosphonic acid dipicolinic acid or derivatives thereof. Suitably the pH of the composition is below 4 preferdbly below 3 most prererdbly below 2 which improves the ar,li",icrobial activity as well as the capability of removing lime deposits or lime soap in for example bath tubs toilet bowls or the like. A low pH also improves the stability of the hydrogen peroxide. However the pH preferably is above about 0.5 most preferably 15 above about 1.
It has SUI~ riai,,yly been found that citric acid unlike most environmental friendly acids does not cause any subslantial decomposilion of the hydrogen peroxide in aque-ous co""~ositions also containing surfactants and phosphon.c acid or dipicolinic acid based complexing agents. It is prefel,ed that apart from citric acid and phosphonic 20 and/or dipicolinic acids or derivatives thereof the co",posilion does not contain any sub-stantial amounts of other organic acids. From an environmental point of view it is also prerel,~d that the composition does not cor"prise any subaldnlial amounts of phosphoric acid or phosphales.
The surfactant facilitates removal of dirt and especially non-ionic surfactants are 25 excellent on removing fat and pigments but they also enhance the ar,li",icrobial effect as they destroy bacterial cell membranes. Preferred surfactants are compatible with hydro-gen peroxide in acidic solutions which means that neither do they cause decomposilion of the hydrogen peroxide nor does the hydrogen peroxide or the acid cause decomposi-tion of the surfactants. Further the surfactants are preferably env;,oh,nenlal friendly and 30 biodegradable.
The co,nposition contains one or several different surfactants. P~eferably it comprises a non-ionic surfactant or an ar"photelic surfactant or a mixture thereof. Al-though not preferred it is also possible to include an-ionic surfactants as an alternative or as a complement.
Plefelled non-ionic surfactants are selected from ethoxylated fatty acids alco-hols amines or amides prefer~bly comprising from 1 to 12 most preferdbly from 4 to 8 mols ethylene oxide per mol acid, alcohol, amine or amide. r~ eferably the acid, alcohol or amide col"p,ises from 7 to 15, most preferably from 9 to 11 carbon atoms. Useful non-ionic surfactants can be high foaming such as an ethoxylated alcohol contai"L,g 11 car-bon atoms and 8 ethylene oxides, or low foaming such as a narrow range ethoxylated 5 alcohol containing 9 carbon atoms and 6 ethylene oxides.
P,ere"ed amphoteric sl"ractanta are selected from derivatives of preferably ali-phatic amines comprising one or more anionic groups such as carboxy, sulfo, or sulfato.
Particularly prefer,ed amphoteric surfactants satisfy the formula:
(CH2)X-COOM
(CH2)~R' 15 wherein x and y are, independently from each other, from 1 to 5, R' is -COOM2 or -OH, M~ and M2 are, i"depender,lly from each other, H, ammonium or an alkali metal such as Na, K or Li, R is a straight or a branched carbon chain having from 1 to 8 carbon atoms or an amide of the formula:
O H
Il I
Rn-C-N-wherein R" is a straight or a brdnched carbon chain having from 1 to 8 carbon atoms. It is pref~r,ed that R' is COOM2 and that R is a straight or a branched carbon chain. Exam-ples of prerer,ed a""~hote,ic surfactants are octylimino di~rop onate and capryloampho ~:~cet~le which are commercially available under the trademarks Ampholak~) YJH40(Akzo Nobel) and Ampholakg) XJO (Akzo Nobel), respectively.
At least one complexing agent based on phosphonic acid, dipicolinic acid or de-rivatives thereof should be included in order to obtain satisfactory storage stability of the hydrogen peroxide. One or several phosphonic acid based complexing agents is pref-erably present in an amount from about 0.5 wt% to about 10 wt%, most preferably from about 1 wt% to about 4 wt% based on the content of hydrogen peroxide. Dipicolinic acid or derivatives thereof may be present in an amount from about 0.25 to about 5 wt%, preferably from about 0.5 to about 2 wt% based on the content of hydrogen peroxide.
The complexing agents also enhance the microbial effect since they chelate cat-ions like ",ag"esium and calcium which have an important role in the bacterial cell. Examples of useful derivatives of dipicolinic acid are picGl;.l c acid, acid, 2,6-pyridine dialdehyde or CA 0222l982 l997-ll-24 2,2-dipyridyl amine. Examples of useful phosphon c acid based compl xing agents are those that are com"~eru;ally available such as 1-hydroxyethylidene-1,1-diphosphon c acid, 1-amifio~tl,ane-1,1-diphosphonic acid, aminotri (methylanephosphon--c acid), ethylene diamine tetra (methyle,)ephosphon-c acid), hexar"etl ,ylene diar"ine tetra 5 (methylenephosphonic acid), diethylanel,ia"tine penta (methylenephosphon.c acid) and diethylenet,iar,line hexa (methylenephosphon c acid), as well as salts thereof. Particularly high stability can be ach-.eved by including both a phosphon.c acid and dipicolinic acid or a derivative thereof.
Preferred phosphon-~ acid based complexing agents are those that are at least 10 partly biodegradable. Thert:fore, the composition pleferably cGillp~ises a complexing agent sEle~1ed from biodegradable 1-aminoalkane-1,1-diphosphonic acids, or salts thereof, pr~fei dbly of the formula:
OX, R~ OX3 O=P--Cl--IP=O
wherein R~ is selected from hydrogen, C1-C4 alkyl and phenyl; R2 and R3, independently from each other, are selected from hydrogen, C~-C22 alkyl, C5-C6 cycloalkyl, phenyl, C7-C~8 alkylphenyl, C7-C,8 phenylalkyl, a C~-C~0 alkanol radical, a carboxy alkyl radical hav-ing up to 10 carbon atoms, wherein R2 and R3 together with the nitrogen atom can form a piperidino, pyrrolidino or a morpholino group; and X~ to X4, independently from each other, are selected from hydrogen, alkali metal and ammonium. Preparation of such phosphonic acids are described in, for example, US 3899496, US 3979385 and nSynthesis of 1-dialkylaminoalkylidene diphosphonic acids and their properties for com-plex formation", Fukuda, M., et al, Yukagaku, Vol. 25, No. 6, pp. 362-64 (1976).Preferably R~ is hydrogen. It is also prefer,dd that R2 and R3 are selected fromhydrogen, C~ to C4 alkyl, or together with the r,it,ugen form a morpholino group. Particu-larly preferred co",F'exing agent are selected from r"or,uholino"~ ane diphosphonic acid, N,N-dimethyl aminodimethyl diphosphonic acid, aminomethyl diphosphon-c acid, or salts thereof, pr~rerably sodium salts.
A composition of the invention can be in the form of a concent,ale intended to be diluted before use. Such a concentrate may suitably contain from about 10 wt% to about 60 wt%, preferably from about 30 wt% to about 50 wt% of hydrogen peroxide, from about 5 wt% to about 30 wt%, prt:r~rdbly from about 10 wt% to about 20 wt% of surfac-tants, from about 0.5 wt% to about 10 wt% pr~fer~bly from about 1 wt% to about 5 wt%
of citric acid, and from about 0.05 wt% to about 10 wt%, prererably from about 1 wt% to about 5 wt% of phosphon e acid based complexing agents, alternatively from about 0.025 to about 5 wt%, p,t:~erably from about 0.5 to about 2.5 wt% of dipicolinic acid or deriva-5 tives thereof. The balance is preferably mainly made up of water. The pH of the concen-trate is suitably from about 0.5 to about 3, preferably from about 1 to about 2. Such a composition is prere~bly diluted from about 10 to about 50 times before use and is then particularly suitable for cleaning and disinfection of hard surfaces, particularly in the food industry where it is i",poilant to destroy human pdll,ogen c as well as product spoiling 10 micro-oryanisills and spores.
A ready to use composition suit-~'e for cleaning, disinfection or stain removal in households suitably contains from about 0.1 wt% to about 10 wt%, preferably from about 4 wt% to about 6 wt% of hydrogen peroxide, from about 0.1 wt% to about 10 wt%, pref-erably from about 2 wt% to about 6 wt% of surfactants, from about 0.1 wt% to about 3 15 wt% preferably from about 0.5 wt% to about 1 wt% of citric acid, and from about 0.01 wt% to about 5 wt%, ple:ferdbly from about 0.1 wt% to about 1 wt% of phosphonic acid based cGi"p'exing agents, alternatively from about 0.005 to about 2.5 wt%, preferably from about 0.05 to about 0.5 wt% of dipicolinic acid or derivatives thereof. The balance is preferably mainly made up of water. The pH of the composition is suitably from about 1 20 to about 4, preferdbly from about 2 to about 3. The composition is very effective for cleaning hard surfaces in kilchens and bathrooms and for removing stains from textiles. It can also be used outdoors for removing or inhibiting growth of mould or algae on wood or other materials. If appropridle, it can be cor"~..,ed with other cleaning agents or deter-gents, such as ordinary alkaline detergents for machine washing.
A composition of the invention can easily be prepared by simply mixing the components to desired concent,;~lions.
The invention also relates to use of a composition as described herein for disin-fection, bleaching, removal of stains from textiles, or removal of lime deposits.
The invention is further illustrated through the following examples which, how-ever, are not intended to limit the scope of the invention. If not otherwise stated, all con-tents and percentages refer to % by weight.
FY~rnple 1: A cG",position according to the invention consisting of an aqueous solution of 5% of hydrogen peroxide, 5% of ethoxylated C~0-C14 fatty alcohols with 7 mols ethylene oxide and 1 mol propylene oxide as a high foai"ing non-ionic surrdctanl, 0.2%
of morpholino",~tl,ane diphosphonic acid disodium salt and 1% of citric acid was pre-pared by mixing the components. The pH was 2.3. The stability of the hydrogen peroxide CA 0222l982 l997-ll-24 was tested by storing the composition 42 days at 40~C. It was found that 95.9% of the hydrogen peroxide remained.
FY~mple ~- A composi~ion according to the invention consisli,lg of an aqueous solution of 5% of hydrogen peroxide, 2.5% of ethoxylated C10-c14 fatty alcohols with 7 5 mols ethylene oxide and 1 mol propylene oxide as a high foaming non-ionic sulrd~tanl, 2.5% of ethoxylated C~6-C~8 amide with 4 mols ethylene oxide as a low roaming non-ionic su,raulanl, 0.2% of mor,uholino",ethane diphosphonic acid disodium salt and 1% of citric acid was prepared by mixing the co",ponenls. The pH was 2.5. The stability of hydrogen peroxid was tested by storing the composition 42 days at 40~C. It was found that 96.6%
10 of the hydlugen peroxide remained.
FY:3rnple 3: A composilion A according to the invention consi~li,lg of an aqueous solution of 4.9% of hydrogen peroxide, 50 g/l of ethoxylated C10-C14 fatty alcohols with 7 mols ethylene oxide and 1 mol propylene oxide as a high foaming non-ionic surfactant, 2 9/l of morpholinomethane diphosphonic acid disodium salt and 10 g/l of citric acid was 15 prepared by mixing the components. The pH was 2.3. A composition B accordi,lg to the invention was prepared in the same way with the exception that 1-hydroxyethylidene-1,1-diphosphon ~ acid was used instead of mor,uhG'i.lomethane diphosphonic acid which gave a pH of 1.8 The stability of the hydrogen peroxide was tested by storing the compositions 830 days at room temperature (about 20-25~C. It was found that the hydrogen peroxide 20 conce, Itldtion after storage was 3.9% in composition A and 2.9% in composition B.
Claims (14)
1. Composition suitable for cleaning, disinfection and/or bleaching c h a r a c t e r i s e d in that it comprises, an acidic aqueous solution of hydrogen peroxide, a surfactant, citric acid, and a complexing agent based on phosphonic acid, dipicolinic acid or derivatives thereof.
2. Composition as claimed in claim 1, c h a r a c t e r i s e d in that the pH of the aqueous solution is below 4.
3. Composition as claimed in claim 2, c h a r a c t e r i s e d in that the pH of the aqueous solution is below 3.
4. Composition as claimed in any one of the claims 1-3, c h a r a c t e r i s e d in that the composition does not comprise any substantial amounts of phosphoric acid or phosphates.
5. Composition as claimed in any one of the claims 1-4, c h a r a c t e r i s e d in that the composition comprises a phosphonic acid based complexing agent.
6. Composition as claimed in any one of the claims 1-5, c h a r a c t e r i s e d in that the composition comprises a complexing agent based on dipicolinic acid or derivatives thereof.
7. Composition as claimed in any one of the claims 1-6, c h a r a c t e r i s e d in that the composition comprises as a complexing agent any of picolinic acid, dipicolinic acid, 2,6-pyridine dialdehyde or 2,2-dipyridyl amine.
8. Composition as claimed in any one of the claims 1-7, c h a r a c t e r i s e d in that the composition comprises a non-ionic surfactant or an amphoteric surfactant or a mixture thereof which is compatible with hydrogen peroxide in acidic solution.
9. Composition as claimed in claim 8, c h a r a c t e r i s e d in that the composition comprises an amphoteric surfactant satisfying the formula:
(CH2)X-COOM1 /
\
(CH2)y-R' wherein x and y are, independently from each other, from 1 to 5, R' is -COOM2 or -OH, M1 and M2 are, independently from each other, hydrogen, ammonium or an alkali metal, R is a straight or a branched carbon chain having from 1 to 8 carbon atoms or an amide of the formula:
wherein R" is a straight or a branched carbon chain having from 1 to 8 carbon atoms.
(CH2)X-COOM1 /
\
(CH2)y-R' wherein x and y are, independently from each other, from 1 to 5, R' is -COOM2 or -OH, M1 and M2 are, independently from each other, hydrogen, ammonium or an alkali metal, R is a straight or a branched carbon chain having from 1 to 8 carbon atoms or an amide of the formula:
wherein R" is a straight or a branched carbon chain having from 1 to 8 carbon atoms.
10. Composition as claimed in claim 9, c h a r a c t e r i s e d in that R' is
11. Composition as claimed in any one of the claims 9-10, c h a r a c t e r i s e d in that R is a straight or a branched carbon chain.
12. Composition as claimed in any one of the claims 1-11, c h a r a c t e r -i s e d in that the composition comprises a chelating agent selected from biodegrad-able 1-aminoalkane-1,1-diphosphonic acids, or salts thereof, of the formula:
¦ ¦ ¦
O=P---C---P=O
¦ ¦ ¦
¦\
wherein R1 is selected from hydrogen, C1-C4 alkyl and phenyl; R2 and R3, independently from each other, are selected from hydrogen, C1-C22 alkyl, C5-C6 cycloalkyl, phenyl, C7-C18 alkylphenyl, C7-C18 phenylalkyl, a C1-C10 alkanol radical, a carboxy alkyl radical hav-ing up to 10 carbon atoms, wherein R1 and R2 together with the nitrogen atom can form a piperidino, pyrrolidino or a morpholino group; and X1 to X4. independently from each other, are selected from hydrogen, alkali metal and ammonium.
¦ ¦ ¦
O=P---C---P=O
¦ ¦ ¦
¦\
wherein R1 is selected from hydrogen, C1-C4 alkyl and phenyl; R2 and R3, independently from each other, are selected from hydrogen, C1-C22 alkyl, C5-C6 cycloalkyl, phenyl, C7-C18 alkylphenyl, C7-C18 phenylalkyl, a C1-C10 alkanol radical, a carboxy alkyl radical hav-ing up to 10 carbon atoms, wherein R1 and R2 together with the nitrogen atom can form a piperidino, pyrrolidino or a morpholino group; and X1 to X4. independently from each other, are selected from hydrogen, alkali metal and ammonium.
13. Composition as claimed in claim 12, c h a r a c t e r i s e d in that the composition comprises a chelating agent selected from morpholinomethane diphos-phonic acid, N,N-dimethyl aminodimethyl diphosphonic acid, aminomethyl diphosphonic acid, or salts thereof.
14. Use of a composition according to any of the claims 1-13 for disinfection, bleaching, removal of stains from textiles, or removal of lime deposits.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9604413A SE9604413D0 (en) | 1996-11-29 | 1996-11-29 | Chemical composition |
| SE9604413-6 | 1996-11-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2221982A1 true CA2221982A1 (en) | 1998-05-29 |
Family
ID=20404814
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002221982A Abandoned CA2221982A1 (en) | 1996-11-29 | 1997-11-24 | Chemical composition |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0845526A3 (en) |
| CA (1) | CA2221982A1 (en) |
| NO (1) | NO975453L (en) |
| SE (1) | SE9604413D0 (en) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6346279B1 (en) | 1998-12-14 | 2002-02-12 | Virox Technologies, Inc. | Hydrogen peroxide disinfectant with increased activity |
| DE69930714T2 (en) * | 1999-01-22 | 2007-03-15 | The Procter & Gamble Co., Cincinnati | Process for treating textiles with a laundry additive |
| US6528471B1 (en) | 1999-01-22 | 2003-03-04 | The Procter & Gamble Company | Process of treating fabrics with a laundry additive |
| DE19961660A1 (en) * | 1999-12-21 | 2001-07-12 | Henkel Kgaa | Care products for washing machines and dishwashers |
| EP1351658B1 (en) | 2001-01-16 | 2005-03-02 | Unilever N.V. | Oral composition |
| NZ534352A (en) | 2002-02-12 | 2006-04-28 | Virox Technologies Inc | Enhanced activity hydrogen peroxide disinfectant |
| 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 |
| ATE438304T1 (en) | 2002-11-15 | 2009-08-15 | Virox Technologies Inc | A HYDROGEN PEROXIDE DISINFECTANT CONTAINING ACID AND/OR ALCOHOL |
| US7459005B2 (en) | 2002-11-22 | 2008-12-02 | Akzo Nobel N.V. | Chemical composition and method |
| US7470444B2 (en) | 2006-04-28 | 2008-12-30 | Delaval, Inc. | Tripe-bleaching composition |
| EP2225175B1 (en) | 2007-12-13 | 2012-12-12 | Akzo Nobel N.V. | Stabilized hydrogen peroxide solutions |
| US8809392B2 (en) | 2008-03-28 | 2014-08-19 | Ecolab Usa Inc. | Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents |
| AU2009230713C1 (en) | 2008-03-28 | 2018-08-02 | Ecolab 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 |
| WO2011078335A1 (en) | 2009-12-25 | 2011-06-30 | 三菱瓦斯化学株式会社 | Etchant and method for manufacturing semiconductor device using same |
| US9321664B2 (en) | 2011-12-20 | 2016-04-26 | Ecolab Usa Inc. | Stable percarboxylic acid compositions and uses thereof |
| JP5980954B2 (en) * | 2012-01-18 | 2016-08-31 | ザ プロクター アンド ギャンブル カンパニー | Acid laundry detergent composition |
| 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 |
| US8822719B1 (en) | 2013-03-05 | 2014-09-02 | Ecolab Usa Inc. | Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring |
| US10165774B2 (en) | 2013-03-05 | 2019-01-01 | Ecolab Usa Inc. | Defoamer useful in a peracid composition with anionic surfactants |
| 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 |
| RU2639433C2 (en) * | 2016-04-12 | 2017-12-21 | Общество с ограниченной ответственностью "АНГАРА ДЕВЕЛОПМЕНТ", ООО "АНГАРА ДЕВЕЛОПМЕНТ" | Solution for deleting deposits of different nature |
| MX2019002072A (en) | 2016-08-30 | 2019-09-16 | Church & Dwight Co Inc | Composition and method for allergen deactivation. |
| US10450535B2 (en) | 2017-10-18 | 2019-10-22 | Virox Technologies Inc. | Shelf-stable hydrogen peroxide antimicrobial compositions |
| EP3922706A1 (en) * | 2020-06-10 | 2021-12-15 | La Superquimica, S.A. | A disinfectant and cleaning composition |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3338260C1 (en) * | 1983-10-21 | 1985-07-25 | Benckiser-Knapsack Gmbh, 6802 Ladenburg | Process and means for bleaching groundwood |
| US4534945A (en) * | 1984-05-03 | 1985-08-13 | Fmc Corporation | Stabilization of high purity hydrogen peroxide |
| DE3531563A1 (en) * | 1985-09-04 | 1987-03-05 | Benckiser Knapsack Gmbh | WOOD FABRICS |
| DE3545909A1 (en) * | 1985-12-23 | 1987-06-25 | Henkel Kgaa | SILICATE- AND MAGNESIUM-FREE ACTIVE SUBSTANCE MIXTURES |
| EP0349153A3 (en) * | 1988-06-28 | 1990-03-14 | The Clorox Company | Stabilizing system for liquid hydrogen peroxide compositions and compositions so stabilized |
| JP2602563B2 (en) * | 1989-12-15 | 1997-04-23 | 花王株式会社 | Liquid oxygen bleach composition |
| DE4232612A1 (en) * | 1992-09-29 | 1994-03-31 | Henkel Kgaa | Removal of magnetite deposits in water-bearing systems |
| RU2066991C1 (en) * | 1993-05-24 | 1996-09-27 | Александр Васильевич Картавченко | Fixed composition for chemical hair-wave |
| EP0634476B1 (en) * | 1993-07-12 | 1999-10-13 | The Procter & Gamble Company | Stable aqueous emulsions of nonionic surfactants with a viscosity controlling agent |
| ES2118445T3 (en) * | 1993-10-26 | 1998-09-16 | Akzo Nobel Nv | AMINOALCANO-DIPHOSPHONIC ACIDS IN BLEACHING OF PAPER MILL |
| EP0829533B1 (en) * | 1996-09-13 | 2004-08-18 | The Procter & Gamble Company | Peroxygen bleaching compositions comprising peroxygen bleach and amino tri(methylene phosphonic acid) (ATMP), suitable for use as a pretreater for fabrics |
-
1996
- 1996-11-29 SE SE9604413A patent/SE9604413D0/en unknown
-
1997
- 1997-11-05 EP EP97203428A patent/EP0845526A3/en not_active Withdrawn
- 1997-11-24 CA CA002221982A patent/CA2221982A1/en not_active Abandoned
- 1997-11-27 NO NO975453A patent/NO975453L/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO975453L (en) | 1998-06-02 |
| EP0845526A3 (en) | 1999-03-03 |
| SE9604413D0 (en) | 1996-11-29 |
| EP0845526A2 (en) | 1998-06-03 |
| NO975453D0 (en) | 1997-11-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2221982A1 (en) | Chemical composition | |
| US6686324B2 (en) | Low-foaming hydrogen peroxide cleaning solution for organic soils | |
| CA1319077C (en) | Liquid detergent containing solid peroxygen bleach | |
| EP2225175B1 (en) | Stabilized hydrogen peroxide solutions | |
| EP1791941A2 (en) | Non-chlorinated concentrated all-in-one acid detergent and method for using the same | |
| US20060089285A1 (en) | Stabilized chlorine bleach in alkaline detergent composition and method of making and using the same | |
| EP0845525B1 (en) | Cleaning, disinfecting and bleaching composition | |
| CA2173438C (en) | Limescale removal compositions | |
| BR112021000739A2 (en) | DETERGENT COMPOSITION | |
| ZA200500274B (en) | Bactericide surfactant compositions | |
| EP0617697B1 (en) | Alkaline hydrogen peroxide formulation | |
| SK5352000A3 (en) | ACID CLEANING COMPOSITIONS CONTAINING ALKOXYLATED AMINES ANDì (54) THEIR USE | |
| JP2908892B2 (en) | Liquid detergent composition | |
| EP0726309B1 (en) | Limescale removal compositions | |
| WO2001065939A1 (en) | Bactericidal compositions comprising a quaternary ammonium salt | |
| CA2454437C (en) | Low-foaming hydrogen peroxide cleaning solution for organic soils | |
| US5677271A (en) | Limescale removal compositions | |
| CA2361741C (en) | Low-foaming hydrogen peroxide cleaning formulation for organic soils | |
| WO1996029451A1 (en) | Cleaning compositions | |
| EP1123375B1 (en) | Thickened liquid hydrogen peroxide bleach compositions | |
| EP1132458B1 (en) | Limescale removing compositions | |
| WO1996035646A1 (en) | Acidic aqueous liquid compositions | |
| JPH07331280A (en) | Bleaching agent composition | |
| MXPA97008619A (en) | Aqueous liquid compositions and aci | |
| KR20140024298A (en) | Stabilization of surfactants against oxidative attack |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |