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
  • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
  • C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
  • C11D17/065—High-density particulate detergent 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
  • C11D1/66—Non-ionic compounds
  • C11D1/74—Carboxylates or sulfonates esters of polyoxyalkylene glycols
• • 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
  • C11D11/00—Special methods for preparing compositions containing mixtures of detergents
  • C11D11/0082—Special methods for preparing compositions containing mixtures of detergents one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads
• • 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
  • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
  • C11D17/0047—Detergents in the form of bars or tablets
  • C11D17/0065—Solid detergents containing builders
  • C11D17/0073—Tablets
  • C11D17/0086—Laundry tablets

Definitions

• the present invention relates to a process for the production of solid detergent and cleaning agents containing surfactants and builders with a high bulk density.
• Modern, compacted detergents or cleaning agents generally have the disadvantage that, owing to their compact structure, they show poorer dissolving behavior in aqueous liquors than, for example, lighter spray-dried detergents or cleaning agents of the prior art. Washing or cleaning agents generally tend to have a poorer rate of dissolution in water, the higher their degree of compaction.
• Structure breakers 10: 1 to 1: 1 can be used.
• polyethylene glycol or polypropylene glycol, sulfates and / or disulfates of polyethylene glycol or polypropylene glycol, sulfosuccinates and / or disulfosuccinates of polyethylene glycol or polypropylene glycol or mixtures of these are used as structure breakers.
• Another known group of gel formation preventers consists of alkylene glycol monoalkyl ethers of the general formula RO (CH 2 CH 2 ) n H, in which R represents a radical with 2 to 8 carbon atoms and n represents a number from 1 to 8. Examples of this group are ethylene glycol monethyl ether and diethylene glycol monobutyl ether.
• the alkoxylated, preferably ethoxylated or ethoxylated and propoxylated, fatty acid alkyl esters preferably having 1 to 4 carbon atoms in the alkyl chain, in particular fatty acid methyl esters, as described, for example, in Japanese Patent Application JP 58/217598 or which are preferably according to processes described in international patent application WO 90/13533 are known that they do not or only to a small extent tend to gel.
• the object of the present invention was to develop a process for the production of solid to granular detergents or cleaning agents with a high bulk density, but which have a compact structure and thus low porosity show improved dissolving properties compared to the known agents with high bulk density, the amount of additives which do not contribute to the washing performance should be kept as low as possible.
• the carboxylic acid alkoxylates of the formula (I) used according to the invention can be prepared by conventional methods, such as, for example, by alkoxylation of the carboxylic acids.
• the fatty acid alkoxylates of the formula (I) can also be prepared by heterogeneously catalyzed direct alkoxylation of fatty acids with alkylene oxide, in particular ethylene oxide. This synthesis method is described in detail in WO 90/13533 and WO 91/15441. The resulting products are characterized by a low OH number, the reaction is carried out in one step and light-colored products are obtained.
• Carboxylic acid alkoxylates of the formula (I) which are derived from fatty acids and in which AO in the formula (I) represents an ethylene oxide unit are preferably used.
• the fatty acids used as starting materials can be obtained from natural oils and fats or produced synthetically.
• the carboxylic acid alkoxylates of the formula (I) are derived from fatty acid cuts, the C 18 carboxylic acid fractions in an amount of up to 75% by weight, based on the carboxylic acid alkoxylate, in particular in an amount of 30 wt .-% to 70 wt .-%, contains.
• the detergents and cleaning agents produced according to the invention can contain, as further ingredients, builders and other surfactants as well as other substances usually contained in such agents.
• the agent prepared according to the invention may contain phosphates, zeolites, water-soluble alkali silicates and organic builders such as polycarboxylates, (co) polymeric polycarboxylates or biodegradable terpolymers and quartpolymers as builder substances.
• the zeolite used is usually finely crystalline, synthetic and bound water-containing zeolite. Suitable are, for example, zeolite A, but also zeolite X and zeolite P and mixtures of A, X and / or P, preferably zeolite of the A type, in detergent quality. Mixtures of zeolite NaA and NaX are also suitable, the proportion of the zeolite NaX in such mixtures advantageously being less than 30%. They have practically no particles larger than 30 ⁇ m and preferably consist at least 80% of particles smaller than 10 ⁇ m.
• Suitable zeolites have an average particle size of less than 10 ⁇ m (measurement method: Eisenhofer diffraction; mean volume distribution), preferably between 1.5 and 4.5 ⁇ m, in particular between 2.0 and 4.0 ⁇ m.
• Their calcium binding capacity which is determined according to the information in German patent application 24 12 837, is in the range from 100 to 200 mg CaO / g.
• the zeolite generally has a water content of 17 to 25% by weight, preferably 18 to 22, in particular 20 to 22% by weight.
• the content of finely divided, in particular crystalline, hydrated zeolite in the agents is preferably 0.5 to 30% by weight, based on the anhydrous active substance.
• the optional water-soluble alkali silicates can be amorphous, X-ray amorphous or crystalline.
• Preferred alkali silicates are the sodium silicates, in particular the amorphous sodium silicates, with a Na 2 O: SiO 2 molar ratio of 1: 1.8 to 1: 3.5.
• Crystalline phyllosilicates of the formula (II) NaMSi x O 2x + 1 + yH 2 O, in which M represents sodium, x a number of 1.9, are preferably used as crystalline silicates, which may be present alone or in a mixture with amorphous silicates to 4 and y is a number from 0 to 20 and are preferred values for x 2, 3 or 4.
• Such crystalline layered silicates are described, for example, in European patent application 164 514.
• Preferred crystalline Layered silicates of the formula (II) are those in which M is sodium and x is 2 or 3.
• both ⁇ - and ⁇ -sodium disilicate Na 2 Si 2 O 5 .yH 2 O are preferred, wherein ⁇ -sodium disilicate can be obtained, for example, by the method described in international patent application WO91 / 08171.
• the content of water-soluble alkali silicates in the agents is preferably 2% by weight to 45% by weight and in particular 10% by weight to 35% by weight, based on the anhydrous active substance.
• Polymeric carboxylates or polymeric carboxylic acids may also be present as further builders. These polymeric carboxylates or carboxylic acids can be present in the compositions according to the invention in an amount of 2 to 15% by weight.
• Suitable polymeric polycarboxylates are, for example, the sodium salts of polyacrylic acid or polymethacrylic acid, for example those with a relative molecular weight of 800 to 150,000 (based on acid).
• Suitable copolymeric polycarboxylates are, in particular, those of acrylic acid with methacrylic acid and of acrylic acid or methacrylic acid with maleic acid. Copolymers of acrylic acid with maleic acid which contain 50 to 90% by weight of acrylic acid and 50 to 10% by weight of maleic acid have proven to be particularly suitable.
• Their relative molecular weight, based on free acids is generally 5,000 to 200,000, preferably 10,000 to 120,000 and in particular 50,000 to 100,000.
• the (co) polymeric polycarboxylates can be used either as a powder or as an aqueous solution, with 20 to 55% by weight aqueous solutions being preferred.
• the content of (co) polymeric polycarboxylates in the agents is preferably 1 to 12% by weight, in particular 2 to 10% by weight.
• biodegradable ter- and quartpolymers for example those which, according to DE-A-43 00 772, as monomers, salts of acrylic acid and maleic acid, as well as vinyl alcohol or vinyl alcohol derivatives, or according to DE-C-42 21 381 Monomeric salts of acrylic acid and 2-alkylallylsulfonic acid and sugar derivatives.
• copolymers are those which are described in German patent applications DE-A-43 03 320 and P 44 17 734.8 and which preferably contain acrolein and acrylic acid / acrylic acid salts or acrolein and vinyl acetate as monomers.
• polycarboxylic acids preferably used in the form of their sodium salts, such as citric acid, adipic acid, succinic acid, glutaric acid, tartaric acid, sugar acid, aminocarboxylic acid, nitrilotriacetic acid (NTA), provided that such use is not objectionable for ecological reasons, and mixtures of these this.
• Preferred salts are the salts of polycarboxylic acids such as citric acid, adipic acid, succinic acid, glutaric acid, tartaric acid, sugar acids and mixtures of these.
• Suitable surfactants are anionic and nonionic, but also cationic, amphoteric or zwitterionic surfactants.
• Suitable anionic surfactants are, for example, C 9 -C 13 alkylbenzenesulfonates, olefin sulfonates, alkanesulfonates, alk (en) ylsulfates, sulfosuccinates, C 6 -C 18 alkyl polyglycol ether sulfonates, C 6 -C 18 fatty acid ester sulfonates, C 6 -C 18 alkyl ether sulfates, glycerol Glycerin ether sulfates, hydroxy mixed ether sulfates, monoglyceride sulfates, sulfotriglycerides, amid acids, C 6 -C 18 fatty acid amide ether sulfates, C 6 -C 18 alkyl (ether) carboxylates, fatty acid isethionates, NC 6 -C 16 acyl sarcosinates, NC 6 -C 18
• Preferred surfactants of the sulfonate type are C 9 -C 13 alkylbenzenesulfonates, olefin sulfonates, ie mixtures of alkene and hydroxyalkanesulfonates and disulfonates such as are obtained, for example, from C 12 -C 18 monoolefins with a terminal or internal double bond by sulfonating with gaseous Sulfur trioxide and subsequent alkaline or acidic hydrolysis of the sulfonation products is considered.
• alkanesulfonates obtained from C 12 -C 18 alkanes, for example by sulfochlorination or sulfoxidation with subsequent hydrolysis or neutralization.
• alkali and, in particular, the sodium salts of the sulfuric acid half-esters of the C 12 -C 18 fatty alcohols are used as alk (en) yl sulfates, for example from coconut fatty alcohol, tallow fatty alcohol, Lauryl, myristyl, cetyl or stearyl alcohol or the C 10 -C 20 oxo alcohols and those half esters of secondary alcohols of this chain length are preferred.
• alk (en) yl sulfates of the chain length mentioned which contain a synthetic, straight-chain alkyl radical prepared on a petrochemical basis and which have a degradation behavior analogous to that of the adequate compounds based on oleochemical raw materials.
• C 16 -C 18 alk (en) yl sulfates are particularly preferred from the point of view of washing technology. It can also be particularly advantageous, and particularly advantageous for machine washing agents, to use C 16 -C 18 -alk (en) yl sulfates in combination with lower melting anionic surfactants and in particular with those anionic surfactants which have a lower Krafft point and relatively low ones Washing temperatures of, for example, room temperature to 40 ° C. show a low tendency to crystallize.
• the compositions therefore contain mixtures of short-chain and long-chain fatty alkyl sulfates, preferably mixtures of C 12 -C 14 fatty alkyl sulfates or C 12 -C 18 fatty alkyl sulfates with C 16 -C 18 fatty alkyl sulfates and in particular C 12 -C 16 -Fatty alkyl sulfates with C 16 -C 18 fatty alkyl sulfates.
• not only saturated alkyl sulfates but also unsaturated alkenyl sulfates with an alkenyl chain length of preferably C 16 to C 22 are used.
• 2,3-Alkyl sulfates which are produced, for example, according to US Pat. Nos. 3,234,258 or 5,075,041 and can be obtained as commercial products from the Shell Oil Company under the name DAN (R) , are also suitable anionic surfactants.
• Preferred anionic surfactants are also the salts of alkylsulfosuccinic acid, which are also referred to as sulfosuccinates or as sulfosuccinic acid esters and which represent monoesters and / or diesters of sulfosuccinic acid with alcohols, preferably fatty alcohols and in particular ethoxylated fatty alcohols.
• Preferred sulfosuccinates contain C 8 to C 18 fatty alcohol residues or mixtures thereof.
• Particularly preferred sulfosuccinates contain a fatty alcohol residue which is derived from ethoxylated fatty alcohols, which in themselves are nonionic surfactants (description see below).
• alk (en) ylsuccinic acid with preferably 8 to 18 carbon atoms in the alk (en) yl chain or salts thereof.
• soaps can be contained in the agents produced according to the invention, in particular saturated fatty acid soaps, the salts of lauric acid, myristic acid, palmitic acid or stearic acid, and in particular from natural fatty acids, e.g. coconut, palm kernel or tallow fatty acids, derived soap mixtures, are suitable.
• the anionic surfactants and the ropes can be present in an amount of 1 to 40% by weight, in particular 8 to 30% by weight, alone or in any mixtures in the composition prepared according to the invention.
• the total surfactant content in the agents according to the invention is preferably above 20% by weight.
• nonionic surfactants are alkoxylated C 8 -C 18 alcohols, alkoxylated fatty acid alkyl esters, alkyl glycosides, amine oxides, polyhydroxy fatty acid amides and the mixtures.
• the nonionic surfactants used are preferably alkoxylated, advantageously ethoxylated, in particular primary alcohols having preferably 8 to 18 carbon atoms and an average of 1 to 12 moles of ethylene oxide (EO) per mole of alcohol, in which the alcohol radical can be linear or preferably methyl-branched in the 2-position or may contain linear and methyl-branched radicals in the mixture, as are usually present in oxo alcohol radicals.
• EO ethylene oxide
• alcohol ethoxylates with linear residues of alcohols of native origin with 12 to 18 carbon atoms, for example from coconut, palm, tallow fat or oleyl alcohol, and an average of 2 to 8 ethylene oxide units (EO) per mole of alcohol are particularly preferred.
• the preferred ethoxylated alcohols include, for example, C 12 -C 14 alcohols with 3 EO or 4 EO, C 9 -C 11 alcohol with 7 EO, C 13 -C 15 alcohols with 3 EO, 5 EO, 7 EO or 8 EO, C 12 -C 18 alcohols with 3 EO, 5 EO or 7 EO and mixtures thereof, such as mixtures of C 12 -C 14 alcohol with 3 EO and C 12 -C 18 alcohol with 5 EO., Die
• the degrees of ethoxylation given represent statistical mean values, which can be an integer or a fraction for a specific product.
• Preferred alcohol ethoxylates have a narrow homolog distribution (narrow range ethoxylates, NRE).
• Nonionic surfactants can also use fatty alcohols with more than 12 EO, examples include tallow fatty alcohol with 14 EO, 25 EO, 30 EO or 40 EO.
• nonionic surfactants which are used either as the sole nonionic surfactant or in combination with other nonionic surfactants, in particular together with alkoxylated fatty alcohols, are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated, fatty acid alkyl esters, preferably with 1 to 4 carbon atoms in the Alkyl chain, in particular fatty acid methyl esters, as described, for example, in Japanese patent application JP 58/217598 or which are preferably prepared by the process described in international patent application WO-A-90/13533.
• alkyl glycosides of the general formula RO (G) x can also be used as further nonionic surfactants, in which R denotes a primary straight-chain or methyl-branched, in particular methyl-branched aliphatic radical having 8 to 22, preferably 12 to 18, C atoms and G is the symbol which stands for a glycose unit with 5 or 6 carbon atoms, preferably for glucose.
• the degree of oligomerization x which indicates the distribution of monoglycosides and oligoglycosides, is any number between 1 and 10.
• Nonionic surfactants of the amine oxide type for example N-coconut alkyl-N, N-dimethylamine oxide and N-tallow alkyl-N, N-dihydroxyethylamine oxide, and the fatty acid alkanolamides can also be suitable.
• the amount of these nonionic surfactants is preferably not more than that of the ethoxylated fatty alcohols, in particular not more than half of them.
• Suitable surfactants are polyhydroxy fatty acid amides of the formula (III), in which R 2 is C0 for an aliphatic acyl radical with 6 to 22 carbon atoms, R 3 for hydrogen, an alkyl or hydroxyalkyl radical with 1 to 4 carbon atoms and [Z] for a linear or branched polyhydroxyalkyl radical with 3 to 10 carbon atoms and 3 to 10 hydroxyl groups stands,
• the polyhydroxy fatty acid amides are known substances which can usually be obtained by reductive amination of a reducing sugar with ammonia, an alkylamine or an alkanolamine and subsequent acylation with a fatty acid, a fatty acid alkyl ester or a fatty acid chloride. With regard to the processes for their preparation, reference is made to US Pat. Nos. 1,985,424, 2,016,962 and 2,703,798 and international patent application WO-A-92/06984.
• the polyhydroxy fatty acid amides are preferably derived from reducing sugars with 5 or 6 carbon atoms, in particular from glucose.
• the nonionic surfactants can be present in the compositions according to the invention in an amount of up to 25% by weight, preferably 2% by weight to 20% by weight.
• Structure breakers can be used as further components. Structure breakers are usually used to improve the processability of funds. Particularly suitable structure breakers are ethoxylated C 8 -C 18 fatty alcohols with 20 to 45 EO, preferably tallow fatty alcohols with 30 and 40 EO, polyethylene glycol or polypropylene glycol, sulfates and / or disulfates of polyethylene glycol or polypropylene glycol, sulfosuccinates and / or disulfosuccinates of polyethylene glycol or polypropylene glycol or mixtures of these.
• the nonionic surfactants and the structure breakers can be used in a ratio of nonionic surfactant to structure breaker of 1: 1 to 15: 1.
• the detergents produced according to the invention preferably contain peroxy bleaching agents and in particular peroxy bleaching agents in combination with bleach activators.
• peroxy bleaching agents sodium perborate tetrahydrate, sodium perborate monohydrate and sodium percarbonate are of particular importance.
• Other useful bleaching agents are, for example, peroxypyrophosphates, citrate perhydrates and H 2 O 2 -producing peracid salts or peracids, such as perbenzoates, peroxophthalates, diperoxyazelaic acid or diperoxydodecanedioic acid.
• the detergents preferably contain 5 to 25% by weight and in particular 10 to 20% by weight of bleach.
• bleach activators can be incorporated into the preparations which form organic peracids with H 2 O 2 .
• Examples include N- or O-acyl compounds, for example polyacylated alkylenediamines, especially tetraacetylethylenediamine, acylated Glycolurils, especially tetraacetylglycoluril, N-acylated hydantoins, hydrazides, triazoles, triazines, urazoles, diketopiperazines, sulfurylamides and cyanurates, moreover carboxylic acid anhydrides, especially phthalic anhydride, carboxylic acid esters, especially sodiumisononanoyloxybenzenesulfonate acetylate, and acyl.
• N- or O-acyl compounds for example polyacylated alkylenediamines, especially tetraacetylethylenediamine, acylated Glycolurils, especially tetraacetyl
• the bleach activator can be coated with coating substances in a known manner or, if necessary with the aid of auxiliaries, granulated or extruded / pelletized and, if desired, contain further additives, for example dye.
• Such granules preferably contain over 70% by weight, in particular from 90% by weight to 99% by weight, of bleach activator.
• a bleach activator is preferably used which forms peracetic acid under the washing conditions.
• TAED tetraacetylethylenediamine
• DADHT 1,5- Diacetyl-2,4-dioxohexahydro-1,3,5-triazine
• Extruded TAED which contains 70 70% by weight of TAED, 15 to 25% by weight of C 12-18 fatty alcohol sulfate and 2 to 6% by weight of soda can also be used.
• the content of bleach activators in the detergents containing bleach is in the usual range, preferably between 1 and 10% by weight and in particular between 3 and 8% by weight.
• suitable ingredients of the agents produced according to the invention are water-soluble inorganic salts such as bicarbonates, carbonates, amorphous silicates or mixtures of these; in particular alkali carbonate and alkali silicate, especially sodium silicate with a molar ratio Na 2 O: SiO 2 of 1: 1 to 1: 4.5, preferably of 1: 2 to 1: 3.5.
• the sodium carbonate content of the agents is preferably up to 20% by weight, advantageously 5 and 15% by weight.
• the other detergent components include foam inhibitors, optical brighteners, enzymes, fabric softening agents, colorants and fragrances.
• Neutral salts can also be present in an amount of up to 20% by weight, their proportion is preferably 10 10% by weight.
• the agent can contain additional graying inhibitors in an amount of 0.1 to 5% by weight, based on the agent.
• Water-soluble colloids of mostly organic nature are suitable as additional graying inhibitors, for example soluble starch preparations and Z.
• Carboxymethyl cellulose (sodium salt), methyl cellulose, methyl hydroxyethyl cellulose and mixtures thereof and polyvinyl pyrrolidone are preferably used.
• Particularly suitable enzymes are those from the class of hydrolases, such as proteases, esterases, lipases or lipolytically active enzymes, amylases, cellulases or other glycosyl hydrolases and mixtures of the enzymes mentioned. All of these hydrolases contribute to the removal of stains, such as stains containing protein, fat or starch, and graying in the laundry. By removing pilling and microfibrils, cellulases and other glycosyl hydrolases can help maintain color and increase the softness of the textile. Oxidoreductases can also be used for bleaching or for inhibiting color transfer.
• hydrolases such as proteases, esterases, lipases or lipolytically active enzymes, amylases, cellulases or other glycosyl hydrolases and mixtures of the enzymes mentioned. All of these hydrolases contribute to the removal of stains, such as stains containing protein, fat or starch, and graying in the laundry. By removing pilling and micro
• Enzymes obtained from bacterial strains or fungi such as Bacillus subtilis, Bacillus licheniformis, Streptomyces griseus and Humicola insolens are particularly suitable.
• Proteases of the subtilisin type and in particular proteases which are obtained from Bacillus lentus are preferably used.
• Enzyme mixtures for example from protease and amylase or protease and lipase or lipolytically active enzymes or protease and cellulase or from cellulase and lipase or lipolytically active enzymes or from protease, amylase and lipase or lipolytically active enzymes or protease, lipase or lipolytic enzymes and cellulase, but especially protease- and / or lipase-containing mixtures or mixtures with lipolytic enzymes of particular interest.
• Known cutinases are examples of such lipolytically active enzymes.
• Peroxidases or oxidases have also proven to be suitable in some cases.
• Suitable amylases include in particular ⁇ -amylases, iso-amylases, pullulanases and pectinases.
• Cellobiohydrolases, endoglucanases and ⁇ -glucosidases, which are also called cellobiases, or mixtures thereof, are preferably used as cellulases. Since the different cellulase types differ in their CMCase and avicelase activities, the desired activities can be set by targeted mixtures of the cellulases.
• the enzymes can be adsorbed on carriers and / or embedded in coating substances in order to protect them against premature decomposition.
• the proportion of enzymes, enzyme mixtures or enzyme granules can be, for example, about 0.1 to 5% by weight, preferably 0.1 to about 2% by weight.
• Suitable stabilizers in particular for peroxygen compounds and enzymes, are the salts, such as neutral sodium salts, of polyphosphonic acids, in particular 1-hydroxyethane-1,1-diphosphonic acid (HEDP), diethylenetriaminepentamethylenephosphonic acid (DETPMP) or ethylenediaminetetramethylenephosphonic acid. These compounds also act as water-soluble complexing agents.
• the phosphonates can be used in amounts of up to 1.5% by weight, but these additives are preferably dispensed with, so that the detergents produced according to the invention have a calculated phosphorus content of 0%.
• Formates such as sodium formate, may be present as further enzyme stabilizers.
• Sodium formate can be used, for example, in an amount of 0.5 to 1% by weight. It is also possible to use proteases which are stabilized with soluble calcium salts and a calcium content of preferably about 1.2% by weight, based on the enzyme.
• proteases which are stabilized with soluble calcium salts and a calcium content of preferably about 1.2% by weight, based on the enzyme.
• boron compounds for example boric acid, boron oxide, borax and other alkali metal borates, is particularly advantageous.
• Suitable foam inhibitors are, for example, organopolysiloxanes and their mixtures with microfine, optionally silanized silica, and paraffins, waxes, microcrystalline waxes and their mixtures with silanized silica. Mixtures of different foam inhibitors can also advantageously be used, e.g. those made of silicone oil, paraffin oil or waxes.
• the foam inhibitors are preferably bound to a granular, water-soluble or dispersible carrier substance.
• the detergents produced according to the invention can contain, for example, derivatives of diaminostilbenedisulfonic acid or their alkali metal salts as optical brighteners, which can be readily incorporated into the dispersion.
• the maximum content of brighteners in the agents produced according to the invention is 0.5% by weight, preferably from 0.02 to 0.25% by weight.
• the joining of solid and liquid detergent or cleaning agent raw materials with simultaneous or subsequent shaping and, if desired, drying can be carried out by all known processes in which detergents and cleaning agents with high Bulk weight, ie with a bulk weight above 500 g / l, preferably above 600 g / l and in particular between 700 and 1,000 g / l, are carried out.
• Liquid nonionic surfactants are particularly suitable as liquid detergent raw materials.
• Examples of such known and preferred processes are granulation processes in which either the solid ingredients of a washing and cleaning agent or a spray-dried washing and cleaning agent or a mixture of spray-dried and non-spray-dried ingredients of washing and cleaning agents, optionally including the additive, in a quick running mixer is compacted and simultaneously mixed or acted upon in this mixer or subsequently in a further device, for example in a fluidized bed, with the liquid constituents.
• a method for the production of granules, a method is preferred in which a premix of detergent components is first prepared.
• This solid, preferably homogeneous premix is extruded in the form of a strand with the addition of a plasticizer and / or lubricant via hole shapes with opening widths of the predetermined granule dimension at high pressures between 25 and 200 bar.
• the strand is cut to the predetermined pellet dimension immediately after exiting the hole shape by means of a cutting device.
• the application of the high working pressure causes the premix to be plasticized during the formation of the granulate and ensures the cutting ability of the freshly extruded strands.
• the premix consists, at least in part, of solid, preferably finely divided, conventional ingredients of detergents and cleaning agents, to which liquid constituents may have been added.
• the solid ingredients can be tower powders obtained by spray drying, but also agglomerates, the mixture components selected in each case as pure substances which are mixed with one another in the finely divided state, and mixtures of these.
• the liquid ingredients are optionally added and then the plasticizer and / or lubricant selected according to the invention is mixed in.
• Preferred plasticizers and / or lubricants are aqueous solutions of polymeric polycarboxylates and highly concentrated anionic surfactant pastes and nonionic surfactants.
• the liquid nonionic surfactants can also be added to the solid premix as a liquid constituent or as a plasticizer and / or lubricant, or they are part of a solid mixture component of the premix, whereby this solid mixture component can consist of a carrier bead that has been exposed to the solution or dispersion.
• the liquid component that is to say not bound to a carrier bead, can be added at any point in the process, for example in the preparation of the premix, but also in the processing of the plasticized premix, but before it passes through the perforated mold (perforated nozzle plate) .
• Kneaders of any configuration for example twin-screw kneaders, can preferably be selected as the homogenizing device.
• the intensive mixing process can in itself lead to a desired temperature increase. Moderately elevated temperatures of, for example, 60 to 70 ° C. are generally not exceeded.
• the premix is preferably fed continuously to a 2-shaft extruder, the housing and the extruder pelletizing head of which are heated to the predetermined extrusion temperature, for example heated to 40 to 60.degree.
• the premix is plasticized at pressures of 25 to 200 bar, extruded in the form of fine strands through the perforated nozzle plate in the extruder head, and finally the extrudate is preferably reduced in spherical to cylindrical granules by means of a rotating knife.
• the hole diameter in the perforated nozzle plate and the strand cut length are matched to the selected granule size.
• the production of granules of an essentially uniformly predeterminable particle size succeeds, and in particular the absolute particle sizes can be adapted to the intended use. In general, particle diameters up to at most 0.8 cm are preferred.
• Important embodiments provide for the production of uniform granules with diameters in the millimeter range, for example in the range from 0.5 to 5 mm and in particular in the range from 0.8 to 3 mm.
• the length / diameter ratio of the chopped-off primary granules is in the range from 1: 1 to about 3: 1. It is also preferred to feed the still plastic, moist primary granules to a further shaping processing step; edges present on the raw granulate are rounded off so that ultimately spherical or at least approximately spherical granules can be obtained.
• small amounts of dry powder for example zeolite powder such as zeolite NaA powder and / or, can also be used in this step.
• This shaping can be carried out in standard rounding machines, for example in rounders with a rotating base plate.
• the granules are then preferably fed to a drying step, for example a fluidized bed dryer.
• Tablets can, for example, be produced in such a way that the builder substances, in particular the water-soluble alkali silicates and, if appropriate, all other constituents are mixed with one another in a mixer and the mixture is advantageously used using conventional tablet presses, for example eccentric presses, hydraulic presses or rotary presses, with pressures in the range from 1 to 300 bar in the range from about 5 to 200 bar and in particular between 10 and 150 bar.
• the compression is preferably carried out without the addition of water.
• the premixes intended for compression can be produced by mixing the individual ingredients, which are at least partially present in pre-assembled form as a granular compound.
• these include, for example, roller-compacted, crystalline, layered or amorphous sodium disilicates which, if appropriate, have been impregnated with liquid to wax-like components, for example nonionic surfactants.
• this enables water-free pre-assembly, which is particularly advantageous.
• break-resistant tablets with good breaking strength which dissolve sufficiently quickly under application conditions, are obtained without any problems.
• the pressing conditions in the respective case are usually to be optimized for the setting of the desired solubility of the tablet with sufficient strength or hardness of the tablet. It applies in a manner known per se that higher compression pressures reduce the solubility of the tablet.
• Preferred tablets have a breaking strength of at least 55 N and in particular at least 60 N. Tablets with breaking strengths above 150 N are also possible.
• a tablet produced in this way preferably has a weight of 10 to 120 g, in particular from 20 to 100 g, the diameter of the tablets usually being less than 100 mm.
• Preferred detergent tablets have a maximum diameter of 80 mm and in particular from 30 to 80 mm.
• These tablets preferably have a weight of 10 to 40 g, with diameters of 20 to 50 mm being preferred.
• the diameter / height ratio of the tablets should be optimized in such a way that the least possible abrasion on the vertical walls of the tabletting apparatus (high diameter / low height) is ensured with sufficient stability and a surface that is not too large (small diameter / high height) .
• Preferred diameter / height ratios of the cylindrical compacts are approximately 0.5: 1 to 10: 1, in particular 1: 1 to 8: 1.
• dry powders are zeolite-NaA powder, but also precipitated or pyrogenic silica such as are commercially available, for example, as Aerosil® or Sipernat® (products from Degussa).
• the process according to the invention can be used to obtain detergents or cleaning agents which have bulk densities above 700 g / l, preferably above 750 g / l and in particular in the range from approximately 800 to approximately 1000 g / l. Despite their compactness and low porosity, the compositions show good dissolving power and a low tendency to gel in aqueous washing liquors.
• a solid premix was prepared from the solid constituents listed in the table below in a batch mixer equipped with a cutter head chopper.
• the mixture was homogenized for 2 minutes and then fed to a twin-screw extruder, the housing of which, including the extruder pelletizing head, was heated to 50 ° C.
• the premix was plasticized and then extruded at a pressure of 120 bar through the extruder perforated die plates into fine strands with a diameter of 1.2 mm, which were chopped into cylindrical granules by means of a knock-out knife. (Length / diameter ratio about 1, hot cut).
• the product obtained was rounded for about 1 minute in a commercially available rounding machine of the type Marumerizer® with the addition of small amounts of zeolite NaA and then dried at a supply air temperature of 70 ° C. in a fluidized bed dryer until an exhaust air temperature of 65 ° C.
• the non-extrudable constituents were then metered in.
• the extruded and dried granules obtained had the compositions shown in Table 1.

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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)

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• 1996
  • 1996-06-19 DE DE1996124415 patent/DE19624415A1/de not_active Withdrawn
• 1997
  • 1997-06-10 EP EP97109360A patent/EP0814149A3/fr not_active Withdrawn

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