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
  • C11D9/00—Compositions of detergents based essentially on soap
  • C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
  • C11D9/22—Organic compounds, e.g. vitamins
  • C11D9/30—Organic compounds, e.g. vitamins containing nitrogen
• • 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
  • C11D3/0005—Other compounding ingredients characterised by their effect
  • C11D3/0026—Low foaming or foam regulating 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
  • C11D3/26—Organic compounds containing nitrogen
  • C11D3/28—Heterocyclic compounds containing nitrogen in the ring

Definitions

• R and R each represents hydrogen or an organic radical containing 1 to 24 carbon atoms and R and R each represent an organic radical containing 2 to 24 carbon atoms; said organic radical designating substituted or unsubstituted straight or branched chain aliphatic, cycloaliphatic or aromatic groups which may contain heteroatoms in their chains.
• This invention relates to suds-suppressing additives for use in detergent and cleaning compositions. More particularly this invention relates to a class of Water-insoluble triazine derivatives constituting effective suds-suppressing agents and to the detergent and cleaning compositions containing such triazine derivatives.
• N-substituted melamines in which each of the three primary nitrogen atoms has at least one hydrocarbon radical containing 4 to 24 carbon atoms.
• the alkylated melamines are usually prepared by the reaction of 1 mole of cyanuric chloride with a three molar quantity of a primary or secondary amine of relatively high molecular weight.
• An object of the instant invention lies in the provision of a class of easily manufactured suds-suppressing agents which can be used for replacing the aforesaid melamines in detergent compositions.
• Another object of the invention is the provision of a class of suds-suppressing agents having a greater effectiveness than the N-substituted melamines.
• Still another object of the invention is the provision of a class of highly effective suds-suppressing compounds whereby the minimum quantity thereof required for adequate suds suppression can be considerably reduced.
• a further object of the invention is the provision of novel detergent and cleaning compositions containing as suds-suppressing agent a water-insoluble triazine derivative.
• R and R each represents hydrogen or an organic radical containing from 1 to 24 carbon atoms
• R and R each represents an organic radical containing from 2 to 24 carbon atoms.
• organic radical designates straight or branched chain aliphatic, cycloaliphatic or aromatic hydrocarbons, which may contain hetero atoms, such as nitrogen, oxygen or sulfur atoms in their chain and which may carry other substituents, such as halogen atoms for example. However, they are not to have any water-solubilizing groups.
• chlorotriazine derivatives for brevity
• the preparation of the compounds defined by the above Formula I and hereinafter designated chlorotriazine derivatives for brevity can be carried out by conventional methods, as for example, by the reaction of 1 mole of cyanuric chloride with a two molar quantity of a primary or secondary amine having the stated number of carbon atoms, starting from amines of the same or different constitution and carbon number.
• chlorotriazine derivatives in which the radicals R and R are both hydrogen and the radicals R and R are each straight-chained saturated or unsaturated hydrocarbon radicals having a C to C chain length.
• These preferred compounds are obtained by the reaction of one mole of cyanuric chloride with a two molar amount of an alkylamine of the stated chain length.
• Alkylamines having 6 to 18 carbon atoms can be prepared in the known manner, as for example, from naturally occurring fatty acid mixtures, such as coconut fatty acid, palm kernel fatty acid, tallow fatty acid, rape oil fatty acid and other fatty acids of vegetable or animal or1g1n.
• naturally occurring fatty acid mixtures such as coconut fatty acid, palm kernel fatty acid, tallow fatty acid, rape oil fatty acid and other fatty acids of vegetable or animal or1g1n.
• the reaction can be carried out by mixing the cyanuric chloride, which can be suspended or dissolved in an inert solvent such as an aromatic hydrocarbon or halogenated hydrocarbon, with a twice-molar quantity of amine; one half of the amine reacting with the triazine radical and the hydrogen chloride released being bonded with the remaining amine to form a hydrochloride. After the addition of 2 moles of a strongly basic compound such as for example, caustic soda solution, the reaction is then carried to completion, with gentle heating, if desired, and the sodium chloride which develops separated by washing.
• an inert solvent such as an aromatic hydrocarbon or halogenated hydrocarbon
• the suds-suppressing properties: of the chlorotriazine derivatives thereby obtained can be further improved if they are employed in a mixture with at least one waterinsoluble melamine derivative of the formula:
• R R and R each represent hydrogen or a hydrocarbon radical having 1 to 24 carbon atoms and R R and R each represent a hydrocarbon radical having 4 to 24 carbon atoms.
• the aforesaid radicals can be satuarted or unsaturated, straight or branch chained, aliphatic, cycloaliphatic or aromatic, and can contain hetero atoms and/or be substituted by halogen atoms.
• the radicals R R and R designate hydrogen and R R and R designate straight-chained, saturated hydrocarbon radicals having 6 to 18 carbon atoms.
• melamine derivatives can be prepared by known methods as, for example, using a method similar to that employed in the preparation of the chlorotriazine derivatives, the amount of amine and of basic compound being increased by 1 mole. However, it is more advantageous to use 2.1 to 2.9 moles of amine per mole of cyanuric chloride, so that mixtures of chlorotriazine and melamine derivatives are directly formed.
• chlorotriazine derivatives and melamine derivatives are characterized by a. synergistic intensification of action, i.e., their suds-suppressing properties exceed considerably the sum of the individual components.
• the amount of the chlorotriazine derivative or of the mixtures of chlorotriazine derivative and melamine derivative which are to be used are regulated by the total quantity of the surface active or wash-active materials, and by the magnitude of the suds-suppressant effect.
• the quantities which have been proven advantageous in practice range from 0.1 to 20% and preferably from 0.2 to of the weight of the wash-active materials. It is possible using still larger amounts, as for example, up to 50% of the weight of the wash-active materials, to achieve a substantially complete suppression of sud formation, however, in the usual detergents this is not generally necessary.
• the mixture ratio of chlorotriazine to melamine derivative amounts to from 10:1 to 1:10. -An optimum effect is achieved at a ratio of chlorotriazine to melamine derivative of from 2:1 to 1:4.
• the afore-stated ratios represent weight ratios.
• the suds inhibitors are suitable for use with different kinds of anionic, ampholytic, cationically active and non-ionic wash-active substances.
• anionic substances which can be used in the detergent and cleaning compositions include alkali soaps of fatty acids, fatty acid condensation products such as derivatives of aminocarboxylic acids; surfactants of the sulfate or sulfonate type, such as primary or secondary alkylsulfates, fatty acid alkanolamide sulfates, fatty acid isoethionates, fatty acid taurides, alkyl sulfonates and olefin sulfonates, alkylbenzene sulfonates, ot-sulfofatty acid esters, and others.
• the chlorotriazine derivatives and mixtures thereof with melamine derivatives are also effective in combination with ampholytic substances, such as the alkyl betaines,, alkyl sulfobetaines and phosphate betaines, as well as cationically active surfactants such as quaternary ammonium salts.
• ampholytic substances such as the alkyl betaines, alkyl sulfobetaines and phosphate betaines
• cationically active surfactants such as quaternary ammonium salts.
• the chlorotriazine derivatives and their mixtures which the melamine derivatives can furthermore be combined with non-ionic wash-active substances, such as alkyl and acyl polyglycol ethers, alkyl phenol polyglycol ethers, fatty acid sugar esters, aminoxides, fatty acid alkanolamines and other fatty acid condensation products, and with saponines.
• the detergent and cleaning agents according to the invention may also contain the customary fillers and additives. These include the washing alkalies, particularly, the pyrophosphates, polyphosphates and phosphates of higher condensation, silicates, carbonates, bicarbonates, borates and hydroxides of alkalies; oxygenyielding bleaches or bleaches containing active chlorine, particularly sodium perborate.
• suitable additives are the known complex compound formers, such as aminopolycarboxylic acids such as aminotriacetic acid, ethylenediaminotetraacetic acid and diethylenetriaminopentaacetic acid, and also aminopolyphosphonic acids such as aminotri-(methylenephosphonic acid) or ethylenediaminotetra-(methylenephosphonic acid) and bydroxyalkyldiphosphonic acids such as l-hydroxyethylenediphosphonic acid.
• aminopolycarboxylic acids such as aminotriacetic acid, ethylenediaminotetraacetic acid and diethylenetriaminopentaacetic acid
• aminopolyphosphonic acids such as aminotri-(methylenephosphonic acid) or ethylenediaminotetra-(methylenephosphonic acid)
• bydroxyalkyldiphosphonic acids such as l-hydroxyethylenediphosphonic acid.
• alkali or ammonium salts can also be used.
• compositions of the invention include oxygen stabilizers such as magnesium silicate, and neutral salts such as sodium sulfate, dirt dispersing agents, particularly cellulose derivatives, optical brighteners and perfumes and dyes.
• oxygen stabilizers such as magnesium silicate
• neutral salts such as sodium sulfate
• dirt dispersing agents particularly cellulose derivatives, optical brighteners and perfumes and dyes.
• the detergent compositions in liquid or paste form can also contain hydrotropic materials such as alkylbenzenesulfonates of low molecular weight, urea and organic solvents.
• the chlorotriazine derivatives and the mixtures thereof with melamine derivatives exert their suds suppressing action even in the presence of the above-named additives.
• chlorotriazine derivatives and the mixtures thereof with melamine derivatives are to be appreciated from the fact that, even in low concentration, they exhibit a considerable suds-suppressing action both in hard and in soft water, with all of known wash-active substances, without in any way diminishing their wash activity.
• the additives according to the invention do not adversely affect the pulverluent properties of the detergents and/or cleaning composition, and they can be easily incorporated into the detergent concentrates as produced for spray drying or into ready-to-use liquid detergents.
• melamine derivatives it is especially advantageous to add the melamine derivatives to the solid detergent components or to a solid component of the detergent composition. This can be done, for example, by mixing the finely divided chlorotriazine derivative or the liquid, melted or dissolved (organic solvents) melamine derivatives with the powdered or granulated detergent or a portion thereof, such as for example, with the sodium perborate, or by spraying the liquid components onto the dry materials.
• composition of the detergents in which the suds inhibitors according to the invention are utilized can vary within wide limits.
• solid or powdered lowsudsing detergents can contain the following principal components:
• alkali silicates and alkali carbonates Per compounds Dispersing agents of high molecular weight, such as carboxymethylcellulose 0.l5 Dyes and perfumes as well as optical brighteners v 0-1 plus stabilizing agents for per compounds, complex compound formers, inorganic neutral salts and moisture Liquid detergents can contain the following as principal components:
• Anhydrous phosphates preferably in the form of potassium salts
• Solubilizers particularly alkylbenzenesulfonates with low alkyl groups 0-10 Dyes and perfumes as well as optical brighteners 0-1 and in addition complex compound formers, water, and,
• organic solvents if desired, organic solvents.
• chlorotriazine and melamine derivatives are not limited to the detergent compositions and quantity ratios given above or in the following examples.
• the suds inhibitors which were employed were chlorotriazine and melamine derivatives which had been obtained by the reaction of cyanuric chloride with the corresponding amounts of primary N-alkylamines of different chain length.
• the moieties R R and R each designates hydrogen, and the moieties R R and R each had chain lengths as follows:
• the suds inhibitors were mixed in the dry state with the perborate, and the latter mixture was then admixed with the spray-dried wash powder.
• the sudsing was tested under close to actual conditions in a fully automatic household washing machine (AEG Lavamat nova 64). This machine was provided with a circular viewing window through which the suds level could be observed and evaluated by means of markings applied thereon. The following scores were used with respect to the suds levels:
• the washing machine was loaded with 3 kg. of clean laundry.
• the detergent concentration amounted to 7.5 g./l. in both wash cycles, and the tap water hardness was 16 dH.
• the results, reported in each instance as averages of three individual measurements, are set out in the following tables. The results show that the chlorotriazine derivatives effectively prevent oversudsing of the wash water, and mixtures thereof with melamine derivatives do so to an even greater extent. Detergents without the additives according to the invention oversudsed in all temperature ranges.
• the suds inhibitors which were employed in the following Examples 12 to 20 were chlorotriazine and melamine derivatives in which the moieties R R and R each represents hydrogen and R R and R each designates 0.1-3% of the suds-inhibitor mixture of claim 1 90% of an inorganic salt selected from the group consisting of pyrophosphates, polyphosphates, silicates, carbonates, bicarbonates and borates of alkacoconut alkyl.
• the sulfobetaine was prepared by reacting lies N-dimethyl-N-alkylamine with propane sultone.
• a detergent composition in liquid form consisting table. essentially of Examples Components (amounts in percent per weight Chlorotriazlne derivative 0.2 0.2 0.2 0.3 0.3 0 3 0.2 0.2 0.4 Melamine derivative 0.3 0.3 0.3 0.4 0.
• Low sudsing detergent consisting essentially of at consisting of anionic, ampholytic, and non-ionic deleast one compound selected from the group consisting of tergents anionic, ampholytic, cationic and non-ionic detergents 0.1-3% of the suds-inhibitor mixture of claim 1 and of 0.1 to 20 wt.
• a suds inhibitor mixture consisting 0-10% of a lower alkyl benzene sulfonate as solubilizer essentially of a water-insoluble triazine derivative of the 01% of a member selected from the group consisting formula I of dyes, perfumes, and optical brighteners.
• a detergent composition comprising:
• R R R R and R represent hydrogen or References Cited hydrocarbon radicals with 1 to 24 carbon atoms
• R and R represent hydrocarbon radicals with 2 to 24 carbon UNITED STATES PATENTS atoms
• R R and R represent hydrocarbon radicals 2,956,898 10/1960 Fleck 260-249.8X with 4 to 24 carbon atoms and wherein the weight ratio 3,422,020 1/ 1969 Schmadel et a1 252-152X of triazine derivative to melamine derivative ranges from 3,429,881 2/ 1969 Kniisli et al 260--249.8 about 10:1 to 1:10. 3,436,394 4/1969 Saul 260249.8
• a detergent composition according to claim 1 where- LEON ROSDOL Primary Examiner in said mixture contains said triazine and melamine derivative in a ratio of 2:1 to 1:4.
• a detergent composition in solid pulverulent form consisting essentially of 5-60% of at least one member selected from the group consisting of anionic, ampholytic, and non-ionic detergents;

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• 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)
• Detergent Compositions (AREA)

Applications Claiming Priority (1)

Publications (1)

Family

ID=7161821

Family Applications (1)

Country Status (11)

Cited By (2)

• 0
  • DK DK126260D patent/DK126260A/da unknown
• 1967
  • 1967-04-01 DE DE19671617127 patent/DE1617127B1/de not_active Withdrawn
  • 1967-12-22 SE SE17747/67A patent/SE344208B/xx unknown
  • 1967-12-27 DK DK652567AA patent/DK126260B/da unknown
• 1968
  • 1968-02-23 FR FR1554518D patent/FR1554518A/fr not_active Expired
  • 1968-03-04 NL NL6803037A patent/NL6803037A/xx unknown
  • 1968-03-27 US US716314A patent/US3600320A/en not_active Expired - Lifetime
  • 1968-03-28 BE BE712893D patent/BE712893A/xx unknown
  • 1968-03-29 AT AT308868A patent/AT278217B/de not_active IP Right Cessation
  • 1968-03-29 CH CH470268A patent/CH492778A/de not_active IP Right Cessation
  • 1968-03-29 GB GB05156/68A patent/GB1222888A/en not_active Expired
  • 1968-03-30 ES ES352210A patent/ES352210A1/es not_active Expired

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