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
• • 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
• • 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
  • C11D3/166—Organic compounds containing borium

Definitions

• This invention relates to alkaline peroxide liquid detergent compositions for fabric washing.
• Borax and sesquicarbonate are frequently incorporated into liquid detergent formulations. Both help to maintain a high wash liquor pH. We have found that each of these materials is incompatible with hydrogen peroxide. Sesquicarbonate gives the required buffering but it also gives rise to rapid decomposition of peroxide. Borax gives lower, but still unacceptably high, levels of peroxide decomposition.
• WO 93/13012 discloses general purpose alkaline bleaching or disinfecting compositions comprising less than 1% of optional amine oxide surfactant, 0.5% borax, and 5 or 10% hydrogen peroxide.
• the pH of the formulations tested is adjusted with sodium hydroxide to the relatively low initial value of 8.5 and the 12 week stability data for the 5% hydrogen peroxide formulation without any surfactant stored at about 30°C shows low loss of peroxide, but it is clear that the buffering is not adequate because the pH drops. There is no suggestion to use anything other than disodium tetraborate decahydrate (borax) as the buffer.
• WO 93/01270 discloses an alkaline aqueous liquid washing agent comprising surfactant, hydrogen peroxide and a water soluble borate chosen from borax and sodium borate, the mole ratio of peroxide : borate being greater than 1.5: 1 and the composition having an initial pH of less than 8 in all the examples.
• the invention resides in the ability of the water soluble borate and other ingredients to give a pH rise to about 9 when the composition is diluted. All formulations contain solvents such as ethanol and propylene glycol. Sodium perborate is not used or suggested.
• an alkali metal perborate or percarbonate salt as a buffering additive in the manufacture of an alkaline peroxide- containing liquid detergent composition, characterised in that the level of the persalt added, based on peroxide equivalent content, is less than 90%, preferably less than 75% and most preferably less than half of the total peroxide equivalent in the composition.
• the buffering additive is dissolved in the Uquid detergent composition as this avoids the problem of suspending a solid component. This is especially advantageous if the composition is isotropic.
• buffering additive is perborate, preferably sodium perborate tetrahydrate or monohydrate.
• an alkaline peroxide liquid detergent composition comprising surfactant, a peroxygen bleach and a soluble buffer, characterised in that the peroxygen bleach is hydrogen peroxide and the buffer is an inorganic persalt selected from alkali metal or alkaline earth salts of perborate and percarbonate, wherein the available oxygen from the hydrogen peroxide exceeds that from the persalt, preferably by at least 2: 1 and most preferably by at least 3: 1.
• compositions of the present invention comprise 5-60% by weight surfactants.
• Peroxide reacts with many surfactants to give reaction products which cause a lowering of the composition pEL
• a wide range of surfactants which may be selected from anionic, cationic, nonionic, zwhterionic and amphoteric surfactants and blends thereof, may be used.
• they may be chosen from any of the classes, sub-classes and specific materials described in "Surface Active Agents" VoL I, by Schwartz & Perry, Interscience 1949 and "Surface Active Agents” Vol.
• Suitable nonionic surfactants include, in particular, the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
• Specific nonionic detergent compounds are alkyl primary or secondary linear or branched alcohols with ethylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and emylenediamine.
• Other so-called nonionic detergent compounds include long chain tertiary amine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
• salting out resistant active materials such as described in EP 328 177, especially the use of alkyl poly glycoside surfactants, such as disclosed in EP 70 074.
• Suitable anionic surfactants are usually water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.
• suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C 8 - 18 ) alcohols produced for example from tallow or coconut oil sodium and potassium alkyl (C 9 - 20 ) benzene sulphonates, particularly sodium linear secondary alkyl (C 10 - 15 ) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C 8 - tg ) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acids amides of methyl taurine;
• an alkali metal soap of a fatty acid especially a soap of an acid having from 12 to 18 carbon atoms, for example oleic acid, ricinoieic acid, and fatty acids derived from castor oil, alkylsuccinic acid, rapeseed oil, groundnut oil coconut oil, palmkernel oil or mixtures thereof.
• the sodium or potassium soaps of these acids can be used.
• the total detergent active material may be present at from 0.5% to 60% by weight of the total composition, for example from 1% to 40% and typically from 2% to 20% by weight. However, one preferred class of compositions comprises from 3-12% of detergent active material based on the weight of the total composition.
• the actual amount of surfactant used will depend on the application, a hard surface cleaner will have a low amount, a fabric pre- treatment composition a rather higher amount and a concentrated detergent a high amount.
• compositions of the invention may be isotropic (unstructured) or structured.
• Structured liquids of the invention may be internally structured whereby the structure is formed by the detergent active materials in the composition or externally structured.
• compositions of the invention are isotropic.
• Viscosity may be regulated by use of one or more hydrotropes. It is preferred to avoid use of 1, 2 diols.
• compositions of the invention may also comprise materials for adjusting the pH.
• weak acids especially organic acids, most preferred is the use of C 1-8 carboxyUc acids, the preferred carboxyUc acid is citric acid.
• the use of these pH lowering agents is especially preferred when the compositions of the invention contain enzymes such as amylases, proteases and lipolases.
• sodium hydroxide preferably pre-sequestered.
• lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids, fabric softeners such as clays, amines and amine oxides, lather depressants, suds regulators, inorganic salts, and, usually present in very minor amounts, opacifiers, fluorescent agents, and optical brighteners, perfumes, germicides, colorants and dyes, and enzymes and enzymatic stabilising agents.
• lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids
• fabric softeners such as clays, amines and amine oxides
• lather depressants such as clays, amines and amine oxides
• suds regulators such as suds regulators, inorganic salts
• opacifiers such as opacifiers, fluorescent agents, and optical brighteners, perfumes, germicides, colorants and dyes, and enzymes and
• soil release agents such as Carboxymethyl cellulose, also known as anti-redeposition agents
• dye transfer inhibiting polymers such as polyvinylpyrroUdone and optical brightening additives (OBAs) such as distyryl biphenyi derivatives.
• compositions of the invention preferably comprise from 10-93% by weight of water, more preferably from 15-90%, most preferably from 40-88%.
• compositions of the present invention may comprise one or more bleach precursor agents.
• a weU-known example of such an agent is TAED.
• the bleach precursor agent is present in the system in at least partly undissolved form.
• the detergent compositions of the invention will be diluted with wash water to form a wash Uquor for instance for use in a washing machine.
• concentration of Uquid detergent composition in the wash Uquor is preferably from 0.05 to 10%, more preferred from 0.1 to 3% by weight.
• the compositions can also be appUed neat to a soiled garment as a pre-treatment.
• the buffering makes them particularly beneficial for such use because they retain all ⁇ linity in storage and use and have a higher detergency against oily stains than an unbuffered or acid Uquid.
• Hard surface cleaners and general purpose cleaners are also used neat; but may be diluted if required.
• compositions may contain a builder, preferably at a level no more than 50%, more preferably at a level of from 5% to 40% of the total composition. If present, such builders can consist of inorganic or organic types, organic builders are preferred.
• the Uquid detergent compositions herein optionally may contain, as a builder, a fatty acid component.
• a fatty acid component Preferably, however, the amount of fatty acid is less than 10% by weight of the composition, more preferably less than 4%.
• Preferred saturated fatty acids have from 10 to 16, more preferably 12 to 14 carbon atoms.
• Preferred unsaturated fatty acids are oleic acid and palmitoleic acid.
• organic builders are poly acids such as citric acid, nitrilotriacetic acid, and mixtures of tartrate monosuccinate with tartrate disuccinate.
• Preferred builders for use herein are citric acid and C 10 _ 16 alk(en)y-l-substituted succinic acid compounds.
• An example of this group of compounds is dodecenyl succinic acid.
• Polymeric carboxylate builders such as polyacrylates, polyhydroxy acrylates and polyacrylates/polymaleates copolymers can also be used.
• compositions herein may also contain other components and/or additives at a level preferably less than about 5%.
• additives which can more preferably be used at levels from 0.03% to 2%, include polyaminocarboxylate additives such as emylenediaminotetracetic acid, diethylenetriamino-pentacetic acid, ethylenediamino disuccinic acid or the water-soluble alkaU metals thereof.
• Other additives useful at these levels include organo-phosphonic acids; particularly preferred are ethylenediamino tetramethylenephosphonic acid, diemylenetriamino pentamethylenephosphonic acid, ammotrimethylenephosphonic acid, and hydroxyethyUdene diphosphonic acid.
• Bleach stabilisers such as dipicolinic acid, sodium stannates and 8-hydroxyquinoUne can also be included in these compositions at these levels, preferably at levels from between 0.01 to 1%.
• sequestrants are disclosed in PCT/GB95/01537 and comprise sodium diethylene triamine penta(methylene phosphonate) such as is sold as Dequest 2066 by Monsanto (and referred to hereinafter as D2066) and 2,2'-dipyridylamine (hereinafter referred to as DPA) and D2066 and 1,2-diaminocyclohexyl tetra (methylene phosphonic acid) and salts thereof (hereinafter referred to as DACH).
• DPA 2,2'-dipyridylamine
• DACH 1,2-diaminocyclohexyl tetra
• sequestering agents gives a universal sequestering performance on transition metal ions. In general these can be separated into two groups, Group A and Group B.
• the Group A sequestering agent preferably comprises one or a mixture of more than one sequestering agents which is effective for stabilising peroxide against decomposition by cobalt II ions under alkaline conditions. They may also be effective for sequestering the other transition metal ions.
• the Group B sequestering agent comprises one or a mixture of more than one sequestering agent which is effective for stabilising peroxide against iron, copper or manganese under alkaline conditions but substantially ineffective in stabilising peroxide against decomposition by cobalt.
• the Group A sequestering agent is preferably selected from compounds having nitrogen donors as Ugands, such as triazacycloalkane compounds especiaUy 1,4,7-triazacyclononanes (TACN), or DPA, as weU as some phosphonate compounds wherein the molecule has Urnited flexibility and appropriate spacing of the Ugands such as DACH. DACH and/or DPA are particularly preferred.
• the group B sequestering agent is preferably a non-cycUc alkylene amino poly(methylene phosphonic acid) or other phosphonic acid compound or salt thereof, especially the foUowing agents under the tradename Dequest : such as Dequest 2006 (aminotris(methylene phosphonic acid)) sodium salt; ethylene diamine tetra (methylene phosphonic acid) or the sodium or potassium salt (e.g. Dequest 2046 which is the sodium salt) and diethylenetriaminepenta (methylene phosphonic acid) (Dequest 2060) or 1 -by droxy ethane- 1, 1-diphosphonic acid sold as Dequest 2010 or analogues with higher alkyUdene groups. D2060 and its sodium salt D2066 are particularly preferred.
• Other Group B useful sequestering agents are those sold under the tradename Briquest from Albright and Wilson.
• the composition is preferably ethanol-free, more preferably free of aU volatile monohy dric alcohols (Le. having flash point about the same as or lower than isopropyl alcohol).
• the concentrate composition is alkaline.
• the composition will have an initial pH of at least 9, preferably 9 to 11 and most preferably 9.5 to 10.
• the pH of the composition after 6 weeks storage at 37° C is preferably still greater than 9 and after 12 weeks storage it is still greater than 8.5.
• the amount of the Group B sequestering agent to be incorporated into the oxidising composition of the invention is at least 0.005% by weight, preferably at least 0.01% by weight. GeneraUy, it will be no greater than 2% by weight, preferably no greater than 1% by weight and most preferably no greater than 0.5% by weight of the total composition.
• the amount of the Group A sequestering agent to be incorporated into the oxidising composition of the invention is at least 0.005% by weight, preferably at least 0.01% by weight, preferably no greater than 2% by weight or no greater than 1% by weight or, more particularly from 0.02 to 0.6% by weight.
• sequestering agents may also be incorporated in the oxidising composition. Where present, such further optional sequestering agents are preferably added in amounts of at least 0.0005% by weight, preferably no greater than 2% by weight, more particularly in the range of from 0.01% to 1.0%, most preferably in the range from 0.02 to 0.6%, by weight.
• Test formulations were prepared using 0.3% sodium percarbonate (Example 1) and 0.5% sodium perborate tetrahydrate (Example 2). They were compared against a control without buffer and comparative example A which contamed 2% sesquicarbonate. Table 1 shows the results. Sodium percarbonate does not give such effective peroxide retention as the sodium perborate. Nevertheless the percarbonate buffering system could be used either alone or in admixture with perborate for detergents with short shelf-life requirements. The sesquicarbonate gave good buffering but the peroxide loss is unacceptable. Further experiments showed that borax gave buffering which was margmaUy worse than Examples 1 and 2, but the peroxide loss was much worse.
• Chlorine is added to mains water for disinfection. Sometimes the level of chlorine is so high that it can lead to fabric dye damage when clothes are repeatedly washed in it.
• the use of low levels of peroxide in a Uquid detergent formulation should cause a reaction with the chlorine which wiU reduce chlorine bleaching.
• Peroxide also provides enhanced bleaching in solution to give reduced damage from dye transfer during the wash.
• Such a "colour safe" formulation requires the use of a buffer for pH stability on storage if it is to deliver satisfactory removal of fatty soil in the wash.
• Colour safe Uquid compositions were prepared containing as surfactant a 10:2 ratio of a Primary alcohol (C 13 . 15 ) ethoxylate, ethoxylated with 7 moles of ethylene oxide : linear alkyl (C 1(M3 ) benzene sulphonic acid; giving a total of 12% actives.
• the composition also included 2%w/w sodium citrate as a builder, 0.02%w/w Acid Blue 80 dye as colorant and 0.20% Tinopal CBS-X a distyryl biphenyl derivative ex Ciba Geigy, as an optical brightening agent.
• compositions had a sequestrant system Control 1 and Example 4 were sequestered with just 0.1% Dequest 2066 and Control 2, Examples 3A and 3B were sequestered with 0.1% Dequest 2066 and 0.03% DPA.
• the initial pH of the Uquids was adjusted to 10 using 50%w/w sodium hydroxide (containing 0.5%w/w Dequest 2066).
• Peroxide was added either as 60% w/w H 2 O 2 solution alone (in the controls) or with 0.5% w/w sodium perborate tetrahydrate as a buffer, to give 1% w/w total hydrogen peroxide equivalents in the controls and the examples.
• the order of addition of the components was perborate, then peroxide solution, then sodium hydroxide.
• the composition of the examples was as foUows:
• Example 3 A and 3B - 0.85% H j O 2 + 0.5%w/w sodium perborate buffer
• Example 4 0.85% H j O 2 + 0.5%w/w sodium perborate buffer
• Examples 3 A and 3B were prepared as identical dupUcates to check the reproducibiUty of the buffered system. Reproducible stabiUty is a key requirement for a commercial system Many of the prior art systems are capable of giving good stabiUty on a one off basis but the effect is not reproducible.
• Buffering is significantly improved in dupUcate examples 3A and 3B containing 0.5% w/w sodium perborate tetrahydrate in solution as a buffer.
• AU examples show similar peroxide stability after 4 weeks storage at 37°C. It is known that peroxide is inherently more stable when the pH is lower. The stabiUty of the two examples containing sodium perborate tetrahydrate is reproducible especiaUy for longer test periods. The beneficial effect of using the soluble persalt as a buffer is obtained for both sequestrant systems.
• compositions which may be formulated using the buffering system which forms the subject of the invention:

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)
• Detergent Compositions (AREA)

Priority Applications (9)

Applications Claiming Priority (2)

Publications (2)

Family

ID=10794376

Family Applications (1)

Country Status (17)

Cited By (2)

Citations (10)

• 1996
  • 1996-05-28 GB GBGB9611062.2A patent/GB9611062D0/en active Pending
• 1997
  • 1997-05-28 WO PCT/GB1997/001450 patent/WO1997045519A2/en not_active Application Discontinuation
  • 1997-05-28 CZ CZ983854A patent/CZ385498A3/cs unknown
  • 1997-05-28 ID IDP971770A patent/ID17361A/id unknown
  • 1997-05-28 PL PL97330116A patent/PL330116A1/xx unknown
  • 1997-05-28 SK SK1603-98A patent/SK160398A3/sk unknown
  • 1997-05-28 IL IL12656097A patent/IL126560A0/xx unknown
  • 1997-05-28 AU AU29689/97A patent/AU2968997A/en not_active Abandoned
  • 1997-05-28 KR KR1019980709643A patent/KR20000016076A/ko not_active Application Discontinuation
  • 1997-05-28 EP EP97924118A patent/EP0923633A2/en not_active Withdrawn
  • 1997-05-28 BR BR9709390A patent/BR9709390A/pt not_active Application Discontinuation
  • 1997-05-28 CN CN97195018A patent/CN1219963A/zh active Pending
  • 1997-05-28 JP JP09541856A patent/JP2000511217A/ja active Pending
  • 1997-05-28 TR TR1998/02460T patent/TR199802460T2/xx unknown
  • 1997-05-28 CA CA002252497A patent/CA2252497A1/en not_active Abandoned
• 1998
  • 1998-11-26 BG BG102958A patent/BG102958A/xx unknown
  • 1998-11-27 NO NO985540A patent/NO985540L/no not_active Application Discontinuation

Patent Citations (10)

Also Published As

Similar Documents

Legal Events