DK143411B - CLEAR LIQUID DETERGENTS CONTAINING TENSIDES BUILDERS HYDROTROPS AND OPTICAL DETAILS - Google Patents
CLEAR LIQUID DETERGENTS CONTAINING TENSIDES BUILDERS HYDROTROPS AND OPTICAL DETAILS Download PDFInfo
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- DK143411B DK143411B DK101872AA DK101872A DK143411B DK 143411 B DK143411 B DK 143411B DK 101872A A DK101872A A DK 101872AA DK 101872 A DK101872 A DK 101872A DK 143411 B DK143411 B DK 143411B
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- 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
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
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- 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
- C11D3/34—Organic compounds containing sulfur
- C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/43—Solvents
Description
14341 114341 1
Den foreliggende opfindelse angår et klart flydende vaskemiddel indeholdende tensider, buildere, hydrotroper og optiske klaremidler.The present invention relates to a clear liquid detergent containing surfactants, builders, hydrotropes and optical brighteners.
Der kendes flydende vaskemidler og specielt flydende vaskemid-5 ler, der indeholder kemiske blegemidler og/eller klaremidler, I den senere tid har sådanne midler indeholdt et overfladeaktivt stof i kombination med et klaremiddel eller blegemiddel, som var dispergeret deri. Det bør imidlertid bemærkes, at en sådan dispersion gav adskillige vanskeligheder med hensyn til 10 ensartet fordeling og endvidere ensartet koncentration af deri indgående optisk klaremiddel.Liquid detergents and especially liquid detergents containing chemical bleaching agents and / or clearing agents are known. Recently, such agents have contained a surfactant in combination with a detergent or bleaching agent dispersed therein. However, it should be noted that such dispersion presented several difficulties with respect to uniform distribution and, furthermore, uniform concentration of optical clarifier contained therein.
Desuden kan man sædvanligvis ikke anvende kemisk blegning til at gøre nitrogenholdige stoffer, der foreligger enten i form af naturlige animalske fibre, såsom uld eller silke eller syn-15 tetiske fibre, såsom polyamider, eksempelvis nylon, hvide eller klare p.gr. af de skadelige virkninger på tøjet eller sådanne blegningsprocessers forholdsvise ineffektivitet.Furthermore, chemical bleaching cannot usually be used to make nitrogenous substances present either in the form of natural animal fibers such as wool or silk or synthetic fibers such as polyamides, for example, nylon, white or clear pg. of the detrimental effects on the clothing or the relative inefficiency of such bleaching processes.
At påføre tøjet en passende fluorescerende forbindelse som i kraft af blålig fluorescens modvirker tøjets matte, gullige 20 skær er en logisk løsning på det problem at forbedre tøjets hvidhed og klarhed. Passende valg og tilfredsstillende tilførsel af det optiske klaremiddel giver imidlertid en række problemer. Den fluorescerende forbindelse skal kunne forliges med og må ikke beskadige tøjet og skal bibringe passende fluo-25 rescens. Den skal kunne forliges med de rensemidler, der anvendes som vaskemedium. Den skal have affinitet for tøjet og skal tilføres i en opløsning som enten ikke hæmmer en sådan affinitet eller fortrinsvis forøger en sådan affinitet. Når den tilføres til tøjet skal den fluorescerende forbindelse des-30 uden blive tilført jævnt og ensaret, da det behandlede tøjs udseende ellers er plettet og uensartet.Applying the clothing to an appropriate fluorescent compound which, by virtue of bluish fluorescence, counteracts the matte, yellowish shades of the clothing is a logical solution to the problem of improving the whiteness and clarity of the clothing. However, appropriate choices and satisfactory application of the optical clarifier present a number of problems. The fluorescent compound must be compatible with and must not damage the clothing and must provide appropriate fluorescence. It must be compatible with the detergents used as detergents. It must have affinity for the clothing and must be applied in a solution which either does not inhibit such affinity or preferably enhances such affinity. However, when applied to the clothing, the fluorescent compound must be applied evenly and uniformly, as the appearance of the treated clothing is otherwise stained and uneven.
Hidtil har det vist sig, at det optiske klaremiddel for at opnå den ønskede ensartede jævne fordeling heraf skal være 2 U3A11 dispergeret i en passende opløsning. Når klaremidlet er en i vand uopløselig forbindelse, giver et sådan krav det yderligere problem, at sådanne klaremidler skal gøres opløselige.Heretofore, it has been found that in order to obtain the desired uniform uniform distribution thereof, the optical clarifier must be 2 U3A11 dispersed in a suitable solution. When the clearing agent is a water-insoluble compound, such a requirement presents the additional problem that such clearing agents must be made soluble.
Af praktiske og økonomiske årsager og på grund af den endelige 5 tilførselsmåde er sådanne klaremiddelprodukter hidtil blevet emballeret og solgt i højkoncentreret form. Opløseliggørelse af i vand uopløselige fluorescerende forbindelser har derfor hidtil været et meget vanskeligt problem,specielt når henses til den kendsgerning, at høje koncentrationer af sådanne for-10 bindeiser skulle inkorporeres i et koncentrat til efterfølgende fortynding med store mængder skylle- eller vaskevand for at opnå en effektiv koncentration af klaremiddel.For practical and economic reasons, and because of the final mode of delivery, such ready-to-use products have so far been packaged and sold in highly concentrated form. Solubilization of water-insoluble fluorescent compounds has therefore been a very difficult problem so far, especially in view of the fact that high concentrations of such compounds should be incorporated into a concentrate for subsequent dilution with large amounts of rinsing or washing water to obtain an effective concentration of clarifying agent.
Fra beskrivelsen til US patent nr. 2.877.185 kendes flydende vaskemidler med indhold af tensider, buildere, hydrotroper og 15 optiske klaremidler, men der indgår ikke heri et co-opløsnings-middelsystem for klaremidlet til opnåelse af den i vaskemidlet ifølge den foreliggende opfindelse overraskende gode og ensartede fordeling og koncentration af klaremidlet og den deraf følgende gode og ensartede klarevirkning på vasketøjet.From the disclosure of U.S. Patent No. 2,877,185, liquid detergents containing surfactants, builders, hydrotropes and optical clarifiers are known, but there is not included a co-solvent system for the detergent to obtain the detergent of the present invention surprisingly good and uniform distribution and concentration of the cleaning agent and the resulting good and uniform cleaning effect on the laundry.
20 Et klart flydende vaskemiddel indeholdende tensider, buildere, hydrotroper og optiske klaremidler ifølge opfindelsen er ejendommelig ved,at det i alt væsentligt består af fra 1 vægt% til 40 vægt% af et vandopløseligt, anionisk syntetisk tensid, fra 1 vægt% til 50 vægt% af et vandopløseligt salt af en ami-25 nocarboxylsyre, fra 1 vægt% til 40 vægt% af en hydrotrop valgt blandt natrium-, kalium- og ammoniumsalte af xylensulfonsyre, toluensulfonsyre, ethylbenzensulfonsyre og cumensulfonsyre, fra 1 vægt% til 20 vægt% af en ethoxyleret Cg_^-fedtalkohol med 2-200 mol ethylenoxid, fra ca. 0,01 vægt% til ca. 0,5 vægt% 30 af et anionisk optisk klaremiddel af stilbentypen og fra 1 vægt% til 20 vægt% af en forbindelse valgt blandt dimethylsulf= oxid og ethylenglycolmonoalkylethere og ethylenglycoldialkyl= ethere, idet nævnte ethere har alkylgrupper med fra 1-4 carbon-atomer, og vand.A clear liquid detergent containing surfactants, builders, hydrotropes and optical brighteners according to the invention is characterized in that it consists essentially of from 1 wt.% To 40 wt.% Of a water-soluble anionic synthetic surfactant, from 1 wt.% To 50 wt. % of a water-soluble salt of an aminocarboxylic acid, from 1% to 40% by weight of a hydrotrope selected from the sodium, potassium and ammonium salts of xylenesulfonic acid, toluenesulfonic acid, ethylbenzenesulfonic acid and cumensulfonic acid, from 1% to 20% by weight an ethoxylated Cg _ fatty alcohol with 2-200 moles of ethylene oxide, from ca. 0.01% by weight to approx. 0.5 wt% 30 of an anionic optical bone of the stilbene type and from 1 wt% to 20 wt% of a compound selected from dimethyl sulfide oxide and ethylene glycol monoalkyl ethers and ethylene glycol dialkyl ethers, said ethers having alkyl groups having from 1-4 carbon atoms , and water.
35 Et vaskemiddel ifølge opfindelsen indeholder som nævnt opti- 143411 3 ske klaremidler. Sådanne optiske klareraidler klassificeres almindeligvis som anioniske fluorescerende farvestoffer, der tjener til at bibringe forøget fluorescens og/eller optiske klaremidler til både hydrofile og hydrofobe fibre. Typiske repræsentative 5 eksempler derpå omfatter derfor dinatrium-Ν,Ν'-bis-2-diethanol= amino-4-phenylamino-l,3,5-triazyl[6]-4,4'-diaminostilben-2, 2' -disulfonat,dinatrium-N,N'-bis-(2-morpholino-4-phenylamino-l,3, 5-triazyl-[6]-4,4'-diaminostilben-2,2'-disulfonat, dinatrium N,N'* bis-(2,4-diphenyl amino-1,3^5-triazyl-[6]-4,4'-diamino-10 stilben-2,2'-disulfonat, dinatrium-4,4'-bis-[4-anilino-6- (N-methyl-N-hydroxyethylamino)-s-triazin-2-ylamino]stilben disulfonat, dinatrium-4,4'-bis-[4-phenyl-2,1,3-triazol-2-yl) stilbendisulfonat, dinatrium-4,4'-bis-[4-anilino-6-(N-2-methyl- 2-hydroxyethylamino)-s-triazin-2-ylamino]stilbendisulfonat og 15 natrium-2-(stilbyl-4'')-naphtho-1",2',4,5)-1,2,3-triazol-2' -sulfonat. Andre egnede anioniske fluorescerende farvestoffer er angivet i beskrivelsen til sydafrikansk patentnr. 66/2892 og i beskrivelsen til US patenterne nr. 2.376.743, nr. 2.612.501, nr. 2.762.801, nr. 2.784.183 og nr. 3.012.971, idet indholdet 20 af disse skrifter skal anses for inkorporeret i den foreliggende tekst ved den ovennævnte omtale heraf. Ligeledes velegnede til anvendelse i forbindelse med det hidtil ukendte klare flydende vaskemiddel ifølge opfindelsen er andre velkendte anioniske klaremidler af stilbentypen ud over de ovenfor an-25 førte.As mentioned, a detergent according to the invention contains optically clearing agents. Such optical clarifiers are generally classified as anionic fluorescent dyes which serve to impart increased fluorescence and / or optical clarifiers to both hydrophilic and hydrophobic fibers. Typical representative examples thereof therefore include disodium Ν, Ν'-bis-2-diethanol = amino-4-phenylamino-1,3,5-triazyl [6] -4,4'-diaminostilben-2,2-disulfonate. , disodium N, N'-bis- (2-morpholino-4-phenylamino-1,3,5-triazyl- [6] -4,4'-diaminostilben-2,2'-disulfonate, disodium N, N ' * bis- (2,4-diphenylamino-1,3,5-triazyl- [6] -4,4'-diamino-stilben-2,2'-disulfonate, disodium-4,4'-bis- 4-Anilino-6- (N-methyl-N-hydroxyethylamino) -s-triazin-2-ylamino] stilben disulfonate, disodium 4,4'-bis- [4-phenyl-2,1,3-triazole-2 -yl) stilbene disulfonate, disodium 4,4'-bis- [4-anilino-6- (N-2-methyl-2-hydroxyethylamino) -s-triazin-2-ylamino] stilbene disulfonate and sodium 2- (stilbyl) -4 '') - naphtho-1 ', 2', 4,5) -1,2,3-triazole-2 'sulfonate. Other suitable anionic fluorescent dyes are disclosed in the specification of South African Patent No. 66/2892 and in U.S. Patent Nos. 2,376,743, 2,612,501, 2,762,801, 2,784,183, and 3,012,971, the contents of which 20 of these writings are to be construed as pored in the present text by the above mention thereof. Also suitable for use in connection with the novel clear liquid detergent of the invention are other well-known anionic type boning agents in addition to those listed above.
Foruden klaremidlet omfatter vaskemidlet ifølge opfindelsen også anioniske overfladeaktive midler. Egnede anioniske tensider omfatter sådanne stoffer som alkylbenzensulfonsyre og salte heraf og forbindelser af formlen alkyl-phenyl-S03-M, 30 hvori alkyl er en alkylgruppe af en fedtsyre M af hydrogen eller et alkalimetal, hvilke forbindelser omfatter en velkendt gruppe anioniske tensider og omfatter natriumdodeeylbenzensul= fonat, kaliumdodecylbenzensulfonat, natriumlaurylbenzensulfo* nat og natriumcetylbenzensulfonat, Andre er alkalimetalsaltene 35 af de højere alkylsulfonsyrer og alkalimetaldialkylsulfosuc- cinaterne, f.eks. natriumdioctylsulfosuecinat og natriumdihe= xylsolfosuccinat, natriumsulfoethylpthalat, natrium-oleyl-p- 143411 4 anisidinsulfonat, natriumtetradecansulfonat, natriumdiisopro-pylnaphthalensulfonat, natriumoctylphenoxyethylsulfat etc. og alkalimetalalkylsulfateme f.eks. natriumlarylsulf at og lignende.In addition to the clearing agent, the detergent of the invention also includes anionic surfactants. Suitable anionic surfactants include such substances as alkylbenzenesulfonic acid and salts thereof and compounds of the formula alkylphenyl-SO3-M, wherein alkyl is an alkyl group of a fatty acid M of hydrogen or an alkali metal, which compounds comprise a well known group of anionic surfactants and include sodium dodecylbenzene sulf = phonate, potassium dodecylbenzenesulfonate, sodium laurylbenzenesulfonate and sodium cetylbenzenesulfonate; Others are the alkali metal salts of the higher alkylsulfonic acids and the alkali metal dialkylsulfosuccinates, e.g. sodium dioctylsulfosuecinate and sodium dihexylsulfosuccinate, sodium sulfoethyl phthalate, sodium oleyl p-anisidine sulphonate, sodium tetradecane sulphonate, sodium diisopropylnaphthalenesulphonate, sodium octylsulphenoxyalphenoxyethyl phenoxyethylene sodium laryl sulfate and the like.
5 Blandt de ovennævnte alkylbenzensulfonsyrer og salte heraf omfatter de foretrukne forbindelser de forbindelser, der kan nedbrydes ad biologisk vej, og som specielt kan karakteriseres ved en lineær alkylsubstituent med 10-22 carbonatomer fortrinsvis fra 12-15 carbonatomer. Det må natruligvis forstås, at 10 carbonkædelængden almindeligvis repræsenterer en gennemsnits- » kædelængde, da fremgangsmåden til fremstilling af sådanne produkter sædvanligvis indebærer anvendelsen af alkyleringsrea-genser af blandet kædelængde. Det er naturligvis klart, at i alt væsentligt rene olefiner såvel som alkyleringsforbindel-15 ser, der anvendes i andre teknikker kan og vil give alkylerede benzensulfonater, hvori alkyIdelen har i alt væsentligt(dvs„ • mindst 99% ) en kædelængde dvs. C'^3, eller .Among the aforementioned alkylbenzenesulfonic acids and salts thereof, the preferred compounds include those which are biodegradable and which can be characterized in particular by a linear alkyl substituent having 10-22 carbon atoms preferably from 12-15 carbon atoms. Of course, it is to be understood that the carbon chain length generally represents an average chain length, since the process of producing such products usually involves the use of mixed chain length alkylation reagents. It will be understood, of course, that substantially pure olefins as well as alkylating compounds used in other techniques can and will give alkylated benzenesulfonates, wherein the alkyl portion has substantially (i.e., at least 99%) a chain length, e.g. C 3 or 3.
De lineære alkylbenzensulfonater karakteriseres yderligere ved stillingen af benzenringen i den lineære alkylkæde, idet 20 enhver af de positions isomere (dvs. α — Ω) kan anvendes og komme i betragtning.The linear alkylbenzene sulfonates are further characterized by the position of the benzene ring in the linear alkyl chain, with any of the position isomers (i.e., α - Ω) being usable and considered.
De lineære alkylbenzensulfonater anvendes almindeligvis og hensigtsmæssigt ved, at sulfonere de tilsvarende alkylbenzen= hydrocarboner som igen kan fremstilles ved at alkylere benzen 25 med et lineært alkylhalogenid, en 1-alken eller en lineær primær eller sekundær alkohol. Rene isomere (af 1-phenylisomeren) fremstilles ved at reducere den acylerede benzen (alkylphenyl= keton) under anvendelse af en modifikation af Wolff-Keshner-reaktionen. 2-phenylisomeren opnås fra n-undecylphenylketon 30 og methylmagnesiumbromid til dannelse af den tertiære alkohol, som dehydratiseres til alkenen og derpå hydrogeneres. 5-phenyl-isomeren opnås på lignende måde fra en n-heptylphenylketon og n-butylmagnesiumbromid. De andre isomere opnås på lignende måde ud fra den passende n-alkylphenylketon og n-alkylmagne-35 siumbromid.The linear alkylbenzene sulfonates are commonly and conveniently used by sulfonating the corresponding alkylbenzene = hydrocarbons which in turn can be prepared by alkylating benzene 25 with a linear alkyl halide, a 1-alkene or a linear primary or secondary alcohol. Pure isomers (of the 1-phenyl isomer) are prepared by reducing the acylated benzene (alkylphenyl = ketone) using a modification of the Wolff-Keshner reaction. The 2-phenyl isomer is obtained from n-undecylphenylketone 30 and methyl magnesium bromide to form the tertiary alcohol which is dehydrated to the alkene and then hydrogenated. The 5-phenyl isomer is similarly obtained from an n-heptylphenyl ketone and n-butyl magnesium bromide. The other isomers are similarly obtained from the appropriate n-alkylphenyl ketone and n-alkylmagnesium bromide.
5 1 A3A115 1 A3A11
Foruden benzensulfonaterne kan man anvende de lavere alkyl (C1-C4) analoge af benzen såsom toluen, xylen, trimethylbenze-nerne, ethylbenzen, isopropylbenzen og lignende. Sulfonaterne anvendes almindeligvis i den vandopløselige saltform, der 5 som kationen omfatter alkalimetallerne, ammonium, og lavere amin og alkanolamin.In addition to the benzenesulfonates, the lower alkyl (C1-C4) analogs of benzene such as toluene, xylene, trimethylbenzene, ethylbenzene, isopropylbenzene and the like can be used. The sulfonates are commonly used in the water-soluble salt form which, as the cation, comprises the alkali metals, ammonium, and lower amine and alkanolamine.
Eksempler på egnede lineære alkylbenzensulfonater: natrium-n-decylben z ensulfonat natrium-n-dodecylbenzensulfonat 10 natrlum-n-tetradecylbenzensulfonat natrium-n-pentadecylbenzensulfonat natrium-n-^hexadecylbenzensul fonat og de tilsvarende lavere alkylsubstituerede homologe af benzen såvel som saltene af de tidligere nævnte kationer. Der kan na-15 turligvis også anvendes blandinger af disse sulfonater sammen med blandinger, som omfatter forbindelser, hvori den lineære alkylkæde er mindre eller længere end det her angivne, forudsat at den gennemsnitlige kædelængde i blandingen er i overensstemmelse med de særlige krav på C^q til C22· 20 De lineære paraffinsulfonater er også en velkendt gruppe forbindelser og omfatter vandopløselige salte (alkalimetal, amin, alkanolamin og ammonium) af: 1-decan-sulfonsyre 1-dodecan-sulfonsyre 25 1-tridecan-sulfonsyre 1-tetradecan-sulfonsyre 1-pentadecan-sulfonsyre 1-hexadecan-su1fonsyre såvel som de andre stillingsisomere af sulfonsyregruppen.Examples of suitable linear alkylbenzene sulfonates: sodium n-decylbenzene sulfonate sodium n-dodecylbenzenesulfonate sodium n-tetradecylbenzenesulfonate sodium n-pentadecylbenzenesulfonate sodium n-hexhexadecylbenzene sulfonate said cations. Naturally, mixtures of these sulfonates may also be used with mixtures comprising compounds in which the linear alkyl chain is less or longer than that given, provided that the average chain length of the mixture is in accordance with the particular requirements of C q to C22 · 20 The linear paraffin sulfonates are also a well-known group of compounds and include water-soluble salts (alkali metal, amine, alkanolamine and ammonium) of: 1-decane-sulfonic acid 1-dodecane-sulfonic acid 1-tridecane-sulfonic acid 1-tetradecane-sulfonic acid 1-pentadecane sulfonic acid 1-hexadecane sulfonic acid as well as the other position isomers of the sulfonic acid group.
30 Udover de ovenfor belyste paraffinsulfonater kan der anvendes 6 U3411 andre i det almindelige område med C^g-til C^-alkyler, idet det mest foretrukne område er fra C^2 til C2Q.In addition to the paraffin sulfonates illustrated above, 6 U3411 others may be used in the ordinary range of C 1-6 to C 2 alkyls, the most preferred range being from C 2 to C 2 Q.
De lineære alkylsulfater, som kommer i betragtning ved nærværende opfindelse, omfatter området fra til . Særlige 5 eksempler omfatter natrium-n-decylsulfat, natrium-n-dodecylsul-fat, natrium-n-hexadecylsulfat, natrium-n -heptadecy1sulfat, na= trium-n-octadecylsulfat og de ethoxylerede derivater (1-100 mol ethylenoxid) og naturligvis de andre vandopløselige saltdannende kationer, der er nævnt ovenfor.The linear alkyl sulfates contemplated by the present invention include the range from to. Particular examples include sodium n-decyl sulfate, sodium n-dodecyl sulfate, sodium n-hexadecyl sulfate, sodium n-heptadecyl sulfate, sodium n-octadecyl sulfate and the ethoxylated derivatives (1-100 moles of ethylene oxide) and of course the other water-soluble salt-forming cations mentioned above.
20 Midlet ifølge den foreliggende opfindelse kan indeholde farvende materialer (farvestofferogpigmenter) og parfumer.The agent of the present invention may contain coloring materials (dyes and pigments) and perfumes.
Endvidere indeholder midlet et vandopløseligt salt af en amino= carboxylsyre såsom f.eks. nitrilotrieddikesyre. Der anvendesFurthermore, the agent contains a water-soluble salt of an amino = carboxylic acid such as e.g. nitrilotriacetic acid. It is used
OISLAND
fortrinsvis trinatriumsaltet deraf som det eneste buildestof 25 i forbindelse med nærværende middel.preferably the trisodium salt thereof as the only building material 25 in connection with the present agent.
Fremstillingen af vaskemidlet ifølge opfindelsen kan ske ved først at sætte klaremidlerne til et opløsningsmiddel såsom en ethylenglycolether eller dimethylsulfoxid. Repræsentative ethylenglycolethere omfatter ethylenglycolmonomethylether, 20 ethylenglycolmonoethylether, ethylenglycolmonopropylether, ethylenglycolmonobutylether og lignende. Efter inkorporeringen af det optiske klaremiddel i enten en ethylenglycolether og/eller dimethylsulfoxid, tilsættes der derefter til blandingen en ethoxyleret fedtalkohol, hvorefter nævnte blanding op-25 varmes til en temperatur fra ca. 26°C til ca.82°C, således at det optiske klaremiddel opløses deri. Repræsentative eth= oxylerede fedtalkoholer, der kan anvendes i forbindelse med nærværende opfindelse omfatter fedtalkoholer indeholdende fra ca. 2-200 mol ethylenoxid såsom f.eks. octanol, nonanol, 30 decanol, undecanol, dodecanol,tridecanol, tetradecanol, pen= tadecanol og lignende. Efter inkorporeringen er de optiske klaremidler i det ovenfor angivne opløsningsmiddelsystem omfattende af en ethylenglycolether og/eller dimethylsulfoxid og en ethoxyleret fedtalkohol under anvendelse af varme, kan 143411 7 nævnte klaremiddelsystem så inkorporeres i de resterende bestanddele således, at der tilvejebringes et klart flydende vaskemiddel.The preparation of the detergent of the invention can be accomplished by first adding the clarifiers to a solvent such as an ethylene glycol ether or dimethyl sulfoxide. Representative ethylene glycol ethers include ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether and the like. Following the incorporation of the optical clarifier into either an ethylene glycol ether and / or dimethyl sulfoxide, an ethoxylated fatty alcohol is then added to the mixture, after which said mixture is heated to a temperature of about 25 ° C. 26 ° C to about 82 ° C so that the optical clarifier dissolves therein. Representative ethoxylated fatty alcohols which may be used in the present invention comprise fatty alcohols containing from ca. 2-200 moles of ethylene oxide such as e.g. octanol, nonanol, decanol, undecanol, dodecanol, tridecanol, tetradecanol, pen = tadecanol and the like. After incorporation, the optical brighteners in the above-mentioned solvent system comprising an ethylene glycol ether and / or dimethylsulfoxide and an ethoxylated fatty alcohol using heat may then incorporate said clearing system into the remaining ingredients such that a clear liquid detergent is provided.
I vaskemidlet ifølge opfindelsen indgår der som nævnt fra ca.The detergent according to the invention includes, as mentioned, from approx.
5 0,01 vægt% til ca. 0,5 vægt% klaremiddel beregnet på basis af vægten af alle bestanddele i det færdige vaskemiddel. Skønt mængderne af de resterende bestanddele ikke er kritiske med henblik på nærværende opfindelse bør det bemærkes, at der i vaskemidlet sædvanligvis indgår fra 1 til ca. 40 vægt% over-10 fladeaktive bestanddele, fra 1-50 vægt% builder, fra 1-40 % hydrotrop, fra 1 til 20% ethoxyleret fedtalkohol, idet resten udgøres af tilsætningsstoffer såsom parfumer, farver og lignende samt vand.5 0.01% by weight to approx. 0.5% by weight of detergent calculated on the basis of the weight of all ingredients in the finished detergent. Although the amounts of the remaining constituents are not critical for the purposes of the present invention, it should be noted that the detergent usually contains from 1 to ca. 40% by weight over-surfactant, from 1-50% by weight builder, from 1-40% hydrotrope, from 1 to 20% ethoxylated fatty alcohol, the remainder being made up of additives such as perfumes, colors and the like, as well as water.
I de efterfølgende eksempler belyses den foreliggende opfin-15 delse nærmere.In the following examples, the present invention is further elucidated.
Eksempel 1Example 1
Der blev fremstillet et klart flydende vaskemiddel indeholdende: Vægt%A clear liquid detergent was prepared containing:% by weight
Natriumtridecylbenzensulfonat 2,5% ethoxyleret fedtalkohol 7,5% nitrilotrieddikesyre,trinatriumsalt 20,0% ethylenglycolmonobutylether 2,0% 4,4'-bis[2,4-dianilino-s-triazinyl-(6)- amino]-stilben-2,2'-disulfonsyre,dinatrium= salt 0,2% 4,4' -bis-t 2- (3-methoxypropylamino) -4-anilino- s-triazinyl-(6)-amino]-stilben-2,2'-disulfon= syre, dinatriumsalt 0,07% 4,4'-bis-[2-morpholino-4-anilino-s-triazinyl- (6)-amino]-stilben-2,2'-disulfonsyre,dinatri= umsalt 0,03% ammoniumcumensulfonat 11,80% vand og farve, en mængde tilstrækkelig til at fylde op til 100,0%Sodium tridecylbenzenesulfonate 2.5% ethoxylated fatty alcohol 7.5% nitrilotriacetic acid, trisodium salt 20.0% ethylene glycol monobutyl ether 2.0% 4,4'-bis [2,4-dianilino-s-triazinyl- (6) -amino] -stilben-2 , 2'-disulfonic acid, disodium = salt 0.2% 4,4'-bis-2- (3-methoxypropylamino) -4-anilino-s-triazinyl- (6) -amino] -stilben-2,2 ' -disulfone = acid, disodium salt 0.07% 4,4'-bis- [2-morpholino-4-anilino-s-triazinyl- (6) -amino] -stilben-2,2'-disulfonic acid, disodium = salted 0 , 03% ammonium cumene sulfonate 11.80% water and color, an amount sufficient to fill up to 100.0%
Det ovennævnte vaskemiddel blev fremstillet ved først at bian- 143411 8 de stilben-klaremidlerne med den ethoxylerede fedtalkohol og ethylenglycolmonobutyletheren. Den resulterende blanding blev derefter opvarmet til 48,8°C i 15 min., og derefter sat til en blanding af deioniseret vand, tinatriumsaltet af nitriltried-5 dikesyre og ammoniumcumensulfonat. De resterende bestanddele blev derefter tilsat, og det resulterende produkt viste sig at være et klart flydende vaskemiddel.The above detergent was prepared by first providing the stilbene clarifiers with the ethoxylated fatty alcohol and the ethylene glycol monobutyl ether. The resulting mixture was then heated to 48.8 ° C for 15 minutes and then added to a mixture of deionized water, the tin sodium salt of nitrile triacetic acid and ammonium cumensulfonate. The remaining ingredients were then added and the resulting product turned out to be a clear liquid detergent.
Eksempel 2Example 2
Midlet fra eksempel 1 blev fremstillet igen, idet dog ammoni--*-0 umcumensulfonatet blev erstattet med natriumxylensulfonat.The agent of Example 1 was prepared again, however, replacing the ammonia - 0 umcumene sulfonate with sodium xylene sulfonate.
Midlet blev fremstillet som beskrevet i eksempel 1 og viste sig at give et stabilt klart flydende vaskemiddel indeholdende klaremidler.The agent was prepared as described in Example 1 and found to provide a stable clear liquid detergent containing clarifying agents.
Eksempel 3Example 3
Midlet fra eksempel 1 blev igen fremstillet, idet ethylengly= colmonobutyletheren blev erstattet med 2vægt% dimethylsulfoxid. Det resulterende vaskemiddel viste sig igen at være en klar væske.The agent of Example 1 was again prepared, replacing the ethylene glycol-colmonobutyl ether with 2% by weight of dimethyl sulfoxide. The resulting detergent again proved to be a clear liquid.
Eksempel 4 20 Midlet fra eksempel 1 blev igen fremstillet, idet de deri anvendte klaremidler blev erstattet med blandinger af et dina= trium-N,N"-bis-(2-diethanolamino-4-phenylamino-l,3,5-triazyl- [6])-4,4'-diaminostilben-2,21-disulfonat, dinatrium-4,4'-bis-[4-anilino-6-(N-methyl-N-hydroxyethylamino)-s-triazin-2-ylami= 25 no>stilbendisulfonat, dinatrium-4,41-bis-(4-phenyl-2,l,3-tri= azol-2-yl)-stilbendisulfonat, dinatrium-4,4'-bis- [4-anilino- 6-Φ-2 -methyl-2-hydroxyethylamino)-s-triazin-2-ylaminol·stilben= disulfonat og natrium-2-(stilbyl-4')-naptho-l,,2,,4,5)-l,2,3-triazol-21-sulfonat. De foregående erstatninger gav klare 30 flydende vaskemidler.Example 4 The agent of Example 1 was again prepared, replacing the clarifiers used therein with mixtures of a disodium-N, N "-bis- (2-diethanolamino-4-phenylamino-1,3,5-triazyl) [6]) - 4,4'-diaminostilben-2,21-disulfonate, disodium 4,4'-bis- [4-anilino-6- (N-methyl-N-hydroxyethylamino) -s-triazine-2- ylami = 25 benzyl benzene disulfonate, disodium 4,41-bis- (4-phenyl-2,1,3-tri = azol-2-yl) -stylbenzene disulfonate, disodium 4,4'-bis- [4-anilino - 6-[(2-methyl-2-hydroxyethylamino) -s-triazin-2-ylaminol] stilben = disulfonate and sodium 2- (stilbyl-4 ') - naptho-1,2,4,5) 1,2,3-triazole-21-sulfonate The preceding substitutions provided clear liquid detergents.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12460171A | 1971-03-15 | 1971-03-15 | |
US12460171 | 1971-03-15 |
Publications (2)
Publication Number | Publication Date |
---|---|
DK143411B true DK143411B (en) | 1981-08-17 |
DK143411C DK143411C (en) | 1981-12-21 |
Family
ID=22415810
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK101872A DK143411C (en) | 1971-03-15 | 1972-03-03 | CLEAR LIQUID DETERGENTS CONTAINING TENSIDES, BUILDERS, HYDROTROPS AND OPTICAL DETERGENTS |
Country Status (17)
Country | Link |
---|---|
US (1) | US3726814A (en) |
AT (1) | ATA170872A (en) |
AU (1) | AU456770B2 (en) |
BE (1) | BE780048A (en) |
CA (1) | CA973310A (en) |
CH (1) | CH571061A5 (en) |
DE (1) | DE2209200B2 (en) |
DK (1) | DK143411C (en) |
ES (1) | ES400498A1 (en) |
FI (1) | FI55350C (en) |
FR (1) | FR2130106B1 (en) |
GB (1) | GB1380107A (en) |
IT (1) | IT961281B (en) |
NL (1) | NL179830B (en) |
NO (1) | NO144243C (en) |
SE (1) | SE394290B (en) |
ZA (1) | ZA72922B (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2326467B2 (en) * | 1972-06-01 | 1979-02-22 | Colgate-Palmolive Co., New York, N.Y. (V.St.A.) | Liquid heavy duty detergent |
US3998750A (en) * | 1975-06-30 | 1976-12-21 | The Procter & Gamble Company | Liquid detergent composition |
DE2609752A1 (en) * | 1976-03-09 | 1977-09-22 | Henkel & Cie Gmbh | Liquid low temp. detergent concentrate - contg. potassium fatty acid salts, ethoxylated alcohol, alkylbenzene sulphonate, brightener and solubiliser |
DE2850382A1 (en) * | 1978-11-21 | 1980-06-04 | Hoechst Ag | COLOR-STABLE DETERGENT WHITENER |
GR76287B (en) * | 1981-09-28 | 1984-08-04 | Procter & Gamble | |
US4687593A (en) * | 1984-12-17 | 1987-08-18 | Monsanto Company | Alkylaryl sulfonate compositions |
US4645623A (en) * | 1984-12-17 | 1987-02-24 | Monsanto Company | Alkylaryl sulfonate compositions |
US4753750A (en) * | 1984-12-31 | 1988-06-28 | Delaware | Liquid laundry detergent composition and method of use |
GB2187749B (en) * | 1986-03-11 | 1990-08-08 | Procter & Gamble | Stable liquid detergent composition hydrophobic brightener |
EP0314630A3 (en) * | 1987-10-30 | 1989-10-25 | Sandoz Ag | Detergent compositions |
US5174927A (en) * | 1990-09-28 | 1992-12-29 | The Procter & Gamble Company | Process for preparing brightener-containing liquid detergent compositions with polyhydroxy fatty acid amines |
GB9408940D0 (en) * | 1994-05-05 | 1994-06-22 | Procter & Gamble | Manual dishwashing compositions |
DE69427905T2 (en) * | 1994-06-10 | 2002-04-04 | Procter & Gamble | Aqueous emulsions with brighteners |
GB9801082D0 (en) * | 1998-01-19 | 1998-03-18 | Unilever Plc | Improvements relating to hard surface cleaners |
US20080146482A1 (en) * | 2006-12-06 | 2008-06-19 | The Procter & Gamble Company | Liquid laundry detergent having improved brightener stability |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2838504A (en) * | 1955-04-21 | 1958-06-10 | Sterling Drug Inc | Benzimidazolylstilbene whitening and brightening agents |
BE553563A (en) * | 1955-12-20 | |||
CA797197A (en) * | 1965-12-09 | 1968-10-22 | Witco Chemical Company | Liquid detergent composition |
AT281242B (en) * | 1966-09-22 | 1970-05-11 | Procter & Gamble | Liquid detergent |
DK130311A (en) * | 1967-11-06 | |||
DE1816348A1 (en) * | 1968-12-21 | 1970-06-25 | Henkel & Cie Gmbh | Washing, bleaching and cleaning agents |
-
1971
- 1971-03-15 US US00124601A patent/US3726814A/en not_active Expired - Lifetime
-
1972
- 1972-02-14 ZA ZA720922A patent/ZA72922B/en unknown
- 1972-02-25 FR FR7206433A patent/FR2130106B1/fr not_active Expired
- 1972-02-26 DE DE2209200A patent/DE2209200B2/en not_active Withdrawn
- 1972-03-01 CH CH299772A patent/CH571061A5/xx not_active IP Right Cessation
- 1972-03-01 BE BE780048A patent/BE780048A/en not_active IP Right Cessation
- 1972-03-02 AT AT170872A patent/ATA170872A/en not_active Application Discontinuation
- 1972-03-02 AU AU39531/72A patent/AU456770B2/en not_active Expired
- 1972-03-03 DK DK101872A patent/DK143411C/en not_active IP Right Cessation
- 1972-03-06 IT IT48794/72A patent/IT961281B/en active
- 1972-03-06 GB GB1032072A patent/GB1380107A/en not_active Expired
- 1972-03-07 ES ES400498A patent/ES400498A1/en not_active Expired
- 1972-03-09 FI FI644/72A patent/FI55350C/en active
- 1972-03-09 SE SE7202971A patent/SE394290B/en unknown
- 1972-03-14 NO NO812/72A patent/NO144243C/en unknown
- 1972-03-14 CA CA137,063A patent/CA973310A/en not_active Expired
- 1972-03-15 NL NLAANVRAGE7203455,A patent/NL179830B/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
NO144243B (en) | 1981-04-13 |
DE2209200B2 (en) | 1981-01-22 |
ZA72922B (en) | 1973-09-26 |
NL7203455A (en) | 1972-09-19 |
IT961281B (en) | 1973-12-10 |
DE2209200A1 (en) | 1972-09-21 |
FI55350B (en) | 1979-03-30 |
DK143411C (en) | 1981-12-21 |
ES400498A1 (en) | 1975-07-16 |
FI55350C (en) | 1979-07-10 |
BE780048A (en) | 1972-07-17 |
NO144243C (en) | 1981-07-22 |
AU456770B2 (en) | 1974-12-10 |
CA973310A (en) | 1975-08-26 |
CH571061A5 (en) | 1975-12-31 |
AU3953172A (en) | 1973-09-06 |
SE394290B (en) | 1977-06-20 |
ATA170872A (en) | 1975-08-15 |
FR2130106A1 (en) | 1972-11-03 |
US3726814A (en) | 1973-04-10 |
FR2130106B1 (en) | 1975-08-29 |
GB1380107A (en) | 1975-01-08 |
NL179830B (en) | 1986-06-16 |
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