WO1993019151A1 - Additif granulaire sans phosphate contenant des tensioactifs non ioniques pour produits de lavage et detergents - Google Patents

Additif granulaire sans phosphate contenant des tensioactifs non ioniques pour produits de lavage et detergents Download PDF

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Publication number
WO1993019151A1
WO1993019151A1 PCT/EP1993/000596 EP9300596W WO9319151A1 WO 1993019151 A1 WO1993019151 A1 WO 1993019151A1 EP 9300596 W EP9300596 W EP 9300596W WO 9319151 A1 WO9319151 A1 WO 9319151A1
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weight
granular
component
free
grain size
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PCT/EP1993/000596
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German (de)
English (en)
Inventor
Lothar Pioch
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Henkel Kommanditgesellschaft Auf Aktien
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Application filed by Henkel Kommanditgesellschaft Auf Aktien filed Critical Henkel Kommanditgesellschaft Auf Aktien
Priority to DE59301514T priority Critical patent/DE59301514D1/de
Priority to EP93906534A priority patent/EP0633923B1/fr
Publication of WO1993019151A1 publication Critical patent/WO1993019151A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246—Silicates, e.g. diatomaceous earth
    • C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
    • C11D3/126—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in solid 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
    • 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
    • C11D11/0088—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 the liquefied ingredients being sprayed or adsorbed onto solid particles
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246—Silicates, e.g. diatomaceous earth
    • C11D3/128—Aluminium silicates, e.g. zeolites
    • 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
    • C11D3/37—Polymers
    • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3761—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid 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
    • C11D3/39—Organic or inorganic per-compounds
    • C11D3/3942—Inorganic per-compounds

Definitions

  • the invention relates to a granular additive for washing and cleaning agents, which consists of two granular powder components of defined composition, on which liquid, semi-solid or solid nonionic surfactants are adsorbed. Both powder components have a porous structure and can absorb up to 30% by weight, based on the additive, of such nonionic surfactants without the free-flowing properties suffering.
  • nonionic surfactants have a very high cleaning power, which makes them particularly suitable for use in low-temperature detergents.
  • their proportion cannot be increased significantly beyond 8 to 10 percent by weight in the generally customary production of detergents by means of spray drying, since this would otherwise result in excessive smoke formation in the exhaust air from the spray towers and inadequate pouring properties of the spray powder.
  • Methods have therefore been developed in which the liquid or melted nonionic surfactant is mixed onto the previously spray-dried powder or sprayed onto a carrier substance.
  • water-soluble builder substances in particular spray-dried phosphates, carbonates, bicarbonates, soluble silicates and borates, and water-insoluble builder substances, such as sodium aluminosilicate (zeolite) and silicon dioxide (Aerosil), have been proposed as carriers, but the known agents often have only a limited ad ⁇ sorption capacity as well as certain technical disadvantages.
  • zeolite sodium aluminosilicate
  • silicon dioxide Aerosil
  • phosphates are undesirable because of their eutrophic properties.
  • Fine powdered zeolites also have only a limited absorption capacity for liquid substances, while special adsorbents, such as diatomaceous earth and aerosil, as inert components do not contribute to the washing action.
  • DE 2418294 discloses detergents which consist of a powder component obtained by hot spray drying and granular sodium perborate tetrahydrate, the latter being impregnated with a defined mixture of nonionic surfactants. Due to the selection of non-ionic surfactants, the granulate is dust-free and free-flowing. According to EP 34 194, the perborate tetrahydrate is treated with nonionic surfactants which contain both ethylene glycol ether groups and propylene glycol ether groups. In addition to good flowability, the granules are notable in particular for being odorless.
  • DE 25 07 926 contains examples of the preparation of premixes, powder mixtures of aluminosilicate (zeolite), perborate and optionally also a bleach activator being sprayed with nonionic surfactants.
  • the resulting granules are then mixed with other powder components, in particular tower spray powder.
  • a certain stickiness of the granules, which can also be transferred to the overall mixture, is a problem here, especially if the admixed tower spray powder contains no phosphates.
  • EP 168 102 discloses a process for the production of high-density detergents in which nonionic surfactants are sprayed onto a powder mixture of sodium perborate monohydrate, zeolite and other builder substances.
  • the base powder is granulated at the same time.
  • Another part of the nonionic surfactants used overall is sprayed onto a second powder component which is free of sodium sulfate and consists of spray-dried granules, the usual surfactants, builder substances and others Contains detergent ingredients.
  • Both the perborate-containing base powder and the spray-dried powder component contain considerable amounts of sodium tripolyphosphate in the agents according to the examples.
  • absorbent carrier grains which consist of several constituents and are usually produced by spray drying. Examples of these are the agents according to US 3849 327, US 3 886098 and US 3 838 027 and US 4 269 722 (DE 27 42 683).
  • these carrier grains which were developed especially for the adsorption of nonionic surfactants, contain considerable amounts of phosphates, which limits their possible uses.
  • Phosphate-free carrier grains are known from DE 32 06 265 and DE 32 06 379. They consist essentially of sodium carbonate or hydrogen carbonate, zeolite, sodium silicate, bentonite and polyacrylate. The high proportion of carbonates, however, favors the formation of calcium carbonate in hard water, while the sodium silicate in conjunction with zeolite considerably deteriorates the dispersibility of the grains in water.
  • EP 184794 discloses a granular adsorbent which is able to absorb high proportions of liquid to pasty detergent constituents, in particular nonionic surfactants, and (based on anhydrous substance) 60 to 80% by weight of zeolite, 0.1 to 8 % By weight of sodium silicate, 3 to 15% by weight of homo- or copolymers of acrylic acid, methacrylic acid and / or maleic acid, 8 to 18% by weight of water and optionally up to 5% by weight contains nonionic surfactants and can be obtained by spray drying. In practice it has been shown that in washing machines with unfavorably designed washing-in devices, the products do not completely dissolve in the course of the washing-in phase and leave residues.
  • EP 425 804 discloses a granular additive for detergents and cleaning agents containing nonionic surfactants, which has improved washing-in behavior and consists of a granular adsorbent (I) and nonionic surfactants (II) adsorbed thereon, where (I) 50 to 75% by weight of finely crystalline zeolite, 2 to 10% by weight of a layered silicate, 3 to 15% by weight of the sodium salt of a (co) polymeric carboxylic acid, optionally up to 10% by weight of sodium sulfate and up to Contains 3% by weight of a surfactant and the rest water and minor constituents and the weight ratio of adsorbent (I) to nonionic surfactants (II) is 2: 1 to 20: 1.
  • component (B) contains a water-soluble soap, which significantly improves the washing-in behavior in the washing machine.
  • the soap-containing additive has a lower absorbency for nonionic surfactants and has a lower self-ignition temperature or an increased flammability.
  • the object of the invention was to provide an additive for granular and phosphate-free detergents and cleaning agents which contains nonionic surfactants and which has both improved wash-in behavior and an increased autoignition temperature or a reduced flammability.
  • the invention accordingly relates to a granular and phosphate-free additive for detergents and cleaning agents, comprising
  • (B) contains a layered silicate.
  • the granular components (A) and (B) and the finished composition have an average particle size of 0.2 to 1.2 mm, preferably 0.3 to 1 mm, in the interest of good flowability and trouble-free flushing behavior.
  • the proportion of particles in the composite with a grain size of less than 0.05 mm is less than 1% by weight, preferably less than 0.1% by weight, the fraction with a grain size below 0.1 mm less than 2% by weight, preferably less than 1% by weight, the fraction with a grain size above 2 mm less than 5% by weight .-%, preferably less than 1 wt .-% and the proportion with a grain size above 1.2 mm less than 10 wt .-%, preferably less than 5 wt .-%.
  • Both components can have the same or a different grain size within the specified limits. Mixing and treating them together with nonionic surfactants can result in a slight agglomeration of the particles, in particular by attaching finely divided components to larger grains, and thus overall a slight increase in the average grain size.
  • the proportion of sodium perborate monohydrate (component A) is preferably 20 to 60% by weight and in particular 30 to 50% by weight.
  • the proportion of component (B) is preferably 35 to 70% by weight and in particular 40 to 60% by weight.
  • the proportion of nonionic component (C) is preferably 7 to 25% by weight and in particular 10 to 20% by weight.
  • the perborate monohydrate is preferably used as a loose, expanded granulate with a liter weight of 450 to 650 g / 1, preferably 500 to 600 g / 1.
  • Granules of this type are notable for good adsorption capacity for liquid to lard-like nonionic surfactants. Loading the granules with the nonionic surfactants generally increases the bulk density by about 50 to 200 g / l, which is in the interest of a higher total bulk weight and a saving in packaging and transport volume.
  • Component (B) likewise preferably consists of a granular, porous material, as can be obtained by spray drying aqueous slurries of water-insoluble or water-soluble salts or salt mixtures. It contains synthetic zeolite of the NaA type in proportions of 45 to 75, preferably 50 to 72% by weight and in particular 55 to 70% by weight (based on anhydrous substance). Mixtures of zeolite NaA and NaX can also be used, the proportion of the zeolite NaX in such mixtures advantageously being below 30%, in particular below 20%. Suitable zeolites have no particles larger than 30 ⁇ m and consist of at least 80% particles less than 10 microns in size.
  • Their average particle size (volume distribution, measurement method: Coulter Counter) is in the range of 1 to 10 ⁇ m.
  • Their calcium binding capacity, which is determined according to DE 24 12837, is in the range from 100 to 200 mg CaO / g.
  • the zeolites can still contain excess alkali from their production.
  • the water content of synthetic zeolites is usually 18 to 22% by weight.
  • Suitable layered silicates which belong to the group of water-swellable smectites, are e.g. those of the general formula
  • the layered silicates can contain hydrogen, alkali and alkaline earth ions, in particular Na + and Ca ++ .
  • the amount of water of hydration is usually in the range of 8 to 20% by weight and depends on the swelling condition or the type of processing.
  • the particle size is in the range from 0.05 to 25 ⁇ m, usually below 10 ⁇ m.
  • Useful sheet silicates are known, for example, from US 3,966,629, US 4,062,647 (DE 23 34899), EP 26529 and EP 28432.
  • Layer silicates are preferably used which are largely free of calcium ions and strongly coloring iron ions due to an alkali treatment.
  • the layer silicate content of component (B) is preferably 3 to 7% by weight.
  • Another advantageous component of component (B) is sodium sulfate, which is calculated as an anhydrous substance and is present in proportions of 0 to 30% by weight, preferably 1 to 25 and in particular 3 to 20% by weight.
  • the sodium sulfate contributes to a considerable improvement in the grain structure of component (B) and the washing-in behavior of the detergent additive and at the same time increases its bulk density, which results in the possibility of saving packaging and transport volume.
  • Another inorganic salt that can be combined with the zeolite is sodium carbonate, which can be present in proportions of up to 20% by weight, based on component (B). With regard to the flushing-in behavior, however, such mixtures are inferior to the mixtures of zeolite and sodium sulfate.
  • component (B) in inorganic salts should be at least 75% by weight, preferably at least 85% by weight (based on component B).
  • component (B) contains organic salts which are particularly advantageous for the grain structure, the grain stability and in particular for the washing-in behavior of the granules and their mixtures with other detergent components.
  • organic salts which are contained in component (B) include the sodium or potassium salts, preferably the sodium salts of homopolymeric and / or copolymeric carboxylic acids.
  • Suitable homopolymers are polyacrylic acid, poly ethacrylic acid and polymaleic acid, polyacrylic acid being preferred.
  • Suitable copolymers are those of acrylic acid with methacrylic acid or copolymers of acrylic acid, methacrylic acid or maleic acid with vinyl ethers, such as vinyl methyl ether or vinyl ethyl ether.
  • the proportion thereof, in the interest of sufficient water solubility is not more than 50 mole percent, preferably less than 30 mole percent.
  • Copolymers of acrylic acid or methacrylic acid with maleic acid as described in more detail in EP 25551, for example, have proven particularly suitable. These are copolymers which contain 40 to 90% by weight of acrylic acid or methacrylic acid and 60 to 10% by weight of maleic acid. Such copolymers are particularly preferred, in which 45 to 85 percent by weight acrylic acid and 55 to 15 percent by weight maleic acid are present.
  • the molecular weight of the homopolymers or copolymers is generally 2,000 to 150,000, preferably 5,000 to 100,000.
  • Their proportion in component (B) is, for example, 1 to 12% by weight, preferably 1.5 to 8% by weight. and in particular 2 to 5% by weight, calculated as the sodium salt.
  • the resistance of the grains to abrasion increases with an increasing proportion of polyacid or its salts. With a proportion from 1.5% by weight, sufficient abrasion resistance is achieved in many cases. Mixtures with 2 to 5% by weight of sodium salt of polyacid have optimal abrasion properties.
  • the zeolite in those cases in which the zeolite is used in the production of the granular component (B) not in powder or spray-dried form, but rather as a moist filter cake, it can contain dispersion stabilizers, as described in more detail in DE 2527388 .
  • Suitable stabilizers are in particular nonionic surfactants with HLB values below 12, such as ethoxylated tallow alcohol with 3 to 8 E0.
  • the proportion of these additives in the powder component (B) can, depending on the zeolite content, be up to 4% by weight, usually 0.3 to 3% by weight. In the final balance, this proportion of component (C) is added.
  • the difference of up to 100% by weight is due to water, which is present in bound form and as moisture, the main amount being bound to the zeolite.
  • a proportion of the water which is about 8 to 18 wt .-% (based on the agent) can be removed at a drying temperature of 145 ° C.
  • Another portion which is between 4 and 8% by weight depending on the zeolite portion, is released at the annealing temperature by about 800 ° C. and corresponds to the water stored in the crystal lattice of the zeolite.
  • the average grain size of component (B) is 0.2 to 1.2 mm, the proportion of the grains below 0.05 mm less than 1% by weight, preferably less than 0.5% by weight and above 2 mm should not be more than 5% by weight.
  • at least 80% by weight, in particular at least 90% by weight, of the grains have a size of 0.1 to 1.2 mm, the proportion of the Grains between 0.1 and 0.05 mm, preferably not more than 3% by weight, in particular less than 1% by weight, the proportion of the grains between 0.1 and 0.2 mm less than 20% by weight , in particular less than 10% by weight and the proportion of the grains between 1.2 and 2 mm is not more than 10% by weight, in particular not more than 5% by weight.
  • the bulk density of component (B) in the preferred embodiment is 400 to 680 g / 1, preferably 450 to 650 g / 1. The adsorption of the nonionic surfactants also increases it by 50 to 200 g / l.
  • the nonionic surfactants adsorbed on the mixture of components (A) and (B) are those which are usually used in washing and cleaning agents.
  • Other suitable additives are organic solvents with which the cleaning ability of detergents and cleaning agents is improved, in particular with regard to greasy soiling, and which can be incorporated into a granular cleaning agent without problems in this way.
  • other substances such as fragrances, finishing agents, optical brighteners and anionic or cationic surfactants, can also be mixed into the mixture of components (A) and (B) after prior dissolution or dispersion in organic solvents or the liquid or melted nonionic surfactants . These substances penetrate into the porous grains together with the solvent or dispersant and are thus protected against interactions with other powder components.
  • Preferred detergent constituents which are bound to the granular mixture and are present together with this as a free-flowing mixture are liquid to pasty nonionic surfactants from the class of the polyglycol ethers, derived from alcohols with 10 to 22, in particular 12 to 18, carbon atoms. These alcohols can be saturated or olefinically unsaturated, linear or methyl-branched in the 2-position (oxo radical).
  • Their reaction products with ethylene oxide (E0) or propylene oxide (PO) are water-soluble or water-dispersible mixtures of compounds with different degrees of alkoxylation. The number of E0 or PO groups corresponds to the statistical mean for technical alkoxylates.
  • ethoxylated fatty alcohols are Ci2-i8 ⁇ coconut alcohols having 3 to 12 EO, Ci6-I 8 -Talgalkohol having 4 to 16 EO, oleyl alcohol containing 4 to 12 EO, and obtainable from other native fatty alcohol mixtures ethoxylation corresponding chain and EO distribution. From the series of ethoxylated oxo alcohols, for example those of the composition C12-15 + 5 to 10 EO and C14-C15 + 5 to 12 EO are suitable.
  • Mixtures of low and highly ethoxylated alcohols are distinguished by increased detergency against both greasy and mineral soiling, for example those made from tallow alcohol with 3 to 6 EO and tallow alcohol with 12 to 16 EO or Ci3_i5-0xoalcohol with 3 to 5 EO and Ci2 -i4-0xoalcohol with 8 to 12 EO.
  • Agents in which the adsorbed nonionic surfactants have both long hydrophobic residues and higher degrees of ethoxylation have particularly favorable flushing properties.
  • the bulk density of the additives according to the invention is preferably between 600 and 950 g / 1, in particular between 650 and 850 g / 1.
  • the advantages of the additives according to the invention lie above all in that they have an increased autoignition temperature or a lower flammability with comparable flushing behavior compared to soap-containing additives of the prior art.
  • additives of the prior art which contain zeolite and (co) polymeric polycarboxylates, but neither soap nor layered silicates, depending on the amount of nonionic surfactant applied, they have an analog to better auto-ignition temperature or flammability and better flushing behavior.
  • An additional advantage of these additives is that they are more free-flowing than the additives of the prior art mentioned.
  • the preparation of component (B) in the preferred embodiment is based, for example, on an aqueous batch containing a total of 40 to 55% by weight of water-free ingredients, which is sprayed into a drop space by means of nozzles and by means of drying gases, which have an inlet temperature of 150 to 280 ° C and an outlet temperature of 50 to 120 ° C, is dried to a removable moisture content at 145 ° C.
  • the aqueous batch can be prepared by mixing the dry or water-containing constituents with the addition of the water required for liquefaction.
  • the salts of the polymeric carboxylic acids the corresponding free acids can also be incorporated and the alkali required for salt formation can be added separately.
  • alkali hydroxide in particular NaOH
  • NaOH alkali hydroxide
  • the content of water-free ingredients in the aqueous mixture is preferably 43 to 50% by weight. Its temperature is expediently 50 to 100 ° C and its viscosity 2000 to 20,000 mPas, usually 8,000 to 14,000 mPas.
  • the atomization pressure is usually 20 to 120 bar, preferably 30 to 80 bar.
  • the drying gas which is generally obtained by burning heating gas or heating oil, is preferably conducted in countercurrent.
  • the inlet temperature measured in the ring channel (ie immediately before entering the lower part of the tower), is 150 to 280 ° C., preferably 170 up to 250 ° C.
  • the exhaust gas laden with moisture leaving the tower has a temperature of 50 to 130 ° C, preferably 55 to 115 ° C.
  • the spray drying is conducted in such a way that the particle size of the spray product has the distribution indicated above.
  • Existing fine and coarse grains are screened before further processing. It has been shown that the rinsing behavior of the adsorbent impregnated with nonionic surfactants deteriorates with increasing proportion of fine grain.
  • Both powder components are combined into a homogeneous mixture and then mixed with liquid or non-ionized liquid that is liquefied by heating. African surfactants or tensidge is treated.
  • the nonionic surfactant is expediently sprayed onto the agitated mixture. Heating the nonionic surfactant to temperatures between 35 and 60 ° C, preferably 40 to 50 ° C, accelerates the adsorption process.
  • the abrasion resistance and constancy of shape of the grains is so high if the specified proportions or production conditions are observed that the freshly prepared, but especially the cooled and, if necessary, reheated, matured grains treated with the liquid additives are treated under the usual spray mixing conditions and can be promoted without the formation of fine particles or coarser agglomerates.
  • the mixing of the two granular components and the subsequent spraying with nonionic surfactants can be carried out continuously or batchwise in conventional mechanical mixing devices, such as drum mixers, fluidized bed mixers or spray mixers.
  • the mixing and spraying process can also be carried out in a single mixing apparatus in the case of continuous operation, the two powder components being combined in a first mixing section and the nonionic component being added in a final mixing section.
  • a particular advantage of the invention is that the adsorption of the liquid nonionic surfactants and their diffusion into the interior of the grain takes place comparatively quickly. Shortly after leaving the mixing apparatus, the grain mixtures have their full flowability and can be processed further without intermediate storage or time-consuming post-ripening process.
  • Suitable powdering agents have a grain size of 0.001 to at most 0.1 mm, preferably less than 0.05 mm and can be present in proportions of 0.03 to 3, preferably 0.05 to 2% by weight, based on that adsorbents loaded with additive are used.
  • finely powdered zeolites for example, finely powdered zeolites, silica airgel (aero- sil ( R )), colorless or colored pigments, such as titanium dioxide and other powder materials already proposed for powdering granules or detergent particles, such as finely powdered sodium tripolyphosphate, sodium sulfate, magnesium silicate and carboxylmethyl cellulose.
  • colorless or colored pigments such as titanium dioxide
  • other powder materials already proposed for powdering granules or detergent particles such as finely powdered sodium tripolyphosphate, sodium sulfate, magnesium silicate and carboxylmethyl cellulose.
  • the granular adsorbents impregnated with the nonionic surfactants or with the mixtures of nonionic surfactant and additive can be mixed with further powdery to granular detergents or detergent components, such as are obtainable for example by spray drying or granulation, or also with bleaches or are mixed with bleach-containing detergents of known composition in any ratio.
  • granular detergents or detergent components such as are obtainable for example by spray drying or granulation
  • bleaches or are mixed with bleach-containing detergents of known composition in any ratio are of great advantage, since an undesired formation of abrasion and dust is avoided.
  • the powder mixtures are in turn stable in storage and do not tend to clump or exude the non-ionic surfactant. When used, they are particularly easy to flush in compared to known agents.
  • the admixed spray powders and granules can also contain sodium sulfate, which is often advantageous for their grain properties, in particular in the absence of phosphates. These admixed detergent components are therefore preferably also phosphate-free.
  • the absorption capacity of the granulate mixture according to the invention for non-ionic surfactants is so high that there is no need to apply these tenides to other mixture components.
  • the additives AI and A2 according to the invention and the comparative additives VI to V4 were examined in particular for their flammability and their flow behavior. All additives contained 40.9% by weight of perborate monohydrate with a bulk density of 460 g / 1 (sieve analysis: greater than 0.8 mm 0%, greater than 0.4 mm 48%, greater than 0.2 mm 47%, greater than 0.1 mm 5%, less than or equal to 0.1 m 0%).
  • the additives AI, VI and V2 each contained 34.1% by weight of component (B); additives A2, V3 and V4 each contained 46.5% by weight of component (B).
  • the mixtures of perborate monohydrate and component (B) were each sprayed with 25% by weight, based on the sprayed additive, of C ⁇ 2-C ⁇ 8 fatty alcohol with 5 EO; in the additives A2, V3 and V4, the mixtures of perborate monohydrate and component (B) were each with 12.6% by weight, based on the sprayed additive, Ci2-C]. 8 fatty alcohol sprayed with 5 E0.
  • the spray-dried component (B) had the composition given in Table 1 in the additives.
  • the flow time of the dry sand after opening of the outflow opening (51 seconds) was set at 100%.
  • the flowability of the additives is given in%, based on this 100% value.

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Abstract

L'invention vise à mettre au point un additif pour produits de lavage et détergents granulaires et sans phosphate, contenant des tensioactifs non ioniques et présentant aussi bien une meilleure tenue au rinçage qu'une température d'inflammation spontanée plus élevée et une combustibilité réduite. On y est parvenu grâce à un additif granulaire et sans phosphate, qui comporte: (A) 10 à 70 % en poids de monohydrate de perborate de sodium ayant une grosseur granulaire moyenne comprise entre 0,2 à 1,2 mm, (B) 25 à 80 % en poids d'un mélange granulaire ayant une grosseur granulaire moyenne comprise entre 0,2 et 1,2 mm, qui est au moins à 75 % en poids de nature inorganique et dépourvu de peroxygène et (rapporté à la substance anhydre dans le constituant B) contient 45 à 75 % en poids de zéolithe synthétique en fins cristaux , 0 à 30 % en poids de sulfate de sodium et 1 à 12 % en poids de sels d'acides carboxyliques homopolymères ou copolymères, (C) 5 à 30 % en poids de tensioactifs non ioniques qui sont liés aux constituants granulaires (A) et (B), (B) comportant 2 à 10 % en poids, rapporté à la substance anhydre dans le constituant (B), d'un silicate stratifié.
PCT/EP1993/000596 1992-03-24 1993-03-15 Additif granulaire sans phosphate contenant des tensioactifs non ioniques pour produits de lavage et detergents WO1993019151A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
DE59301514T DE59301514D1 (de) 1992-03-24 1993-03-15 Granulares, nichtionische tenside enthaltendes, phosphatfreies additiv für wasch- und reinigungsmittel
EP93906534A EP0633923B1 (fr) 1992-03-24 1993-03-15 Additif granulaire sans phosphate contenant des tensioactifs non ioniques pour produits de lavage et detergents

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP4209435.6 1992-03-24
DE4209435A DE4209435A1 (de) 1992-03-24 1992-03-24 Granulares, nichtionische Tenside enthaltendes, phosphatfreies Additiv für Wasch- und Reinigungsmittel

Publications (1)

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WO1993019151A1 true WO1993019151A1 (fr) 1993-09-30

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PCT/EP1993/000596 WO1993019151A1 (fr) 1992-03-24 1993-03-15 Additif granulaire sans phosphate contenant des tensioactifs non ioniques pour produits de lavage et detergents

Country Status (6)

Country Link
EP (1) EP0633923B1 (fr)
AT (1) ATE133447T1 (fr)
DE (2) DE4209435A1 (fr)
ES (1) ES2083281T3 (fr)
TR (1) TR26864A (fr)
WO (1) WO1993019151A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0816485A1 (fr) * 1996-07-04 1998-01-07 The Procter & Gamble Company Procédé de préparation de compositions détergentes
US6056905A (en) * 1997-06-16 2000-05-02 Lever Brothers Company Division Of Conopco, Inc. Production of detergent granulates
US6133223A (en) * 1997-06-27 2000-10-17 Lever Brothers Company, Division Of Conopco, Inc. Production of detergent granulates
US6274544B1 (en) 1997-06-16 2001-08-14 Lever Brothers Company, Division Of Conopco, Inc. Production of detergent granulates
ITMI20130757A1 (it) * 2013-05-09 2014-11-10 Unicalce S P A Composizione granulare a ridotta segregabilita', suo procedimento di preparazione e relativi usi

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0168102A2 (fr) * 1984-07-06 1986-01-15 Unilever N.V. Procédé de préparation d'une composition détergente en poudre à densité en vrac élevée
EP0276705A2 (fr) * 1987-01-24 1988-08-03 Henkel Kommanditgesellschaft auf Aktien Agglomérat poreux de couche de silicate/sulfate de sodium
WO1990014412A1 (fr) * 1989-05-22 1990-11-29 Henkel Kommanditgesellschaft Auf Aktien Additif granulaire sans phosphates contenant des agents tensio-actifs non ioniques pour produit a lessive
EP0425804A2 (fr) * 1989-11-02 1991-05-08 Henkel KGaA Additif granulaire contenant un agent tensioactif pour détergent et agent de nettoyage avec des propriétés de rinçage améliorées

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0168102A2 (fr) * 1984-07-06 1986-01-15 Unilever N.V. Procédé de préparation d'une composition détergente en poudre à densité en vrac élevée
EP0276705A2 (fr) * 1987-01-24 1988-08-03 Henkel Kommanditgesellschaft auf Aktien Agglomérat poreux de couche de silicate/sulfate de sodium
WO1990014412A1 (fr) * 1989-05-22 1990-11-29 Henkel Kommanditgesellschaft Auf Aktien Additif granulaire sans phosphates contenant des agents tensio-actifs non ioniques pour produit a lessive
EP0425804A2 (fr) * 1989-11-02 1991-05-08 Henkel KGaA Additif granulaire contenant un agent tensioactif pour détergent et agent de nettoyage avec des propriétés de rinçage améliorées

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0816485A1 (fr) * 1996-07-04 1998-01-07 The Procter & Gamble Company Procédé de préparation de compositions détergentes
US6056905A (en) * 1997-06-16 2000-05-02 Lever Brothers Company Division Of Conopco, Inc. Production of detergent granulates
US6274544B1 (en) 1997-06-16 2001-08-14 Lever Brothers Company, Division Of Conopco, Inc. Production of detergent granulates
US6429184B1 (en) 1997-06-16 2002-08-06 Lever & Brothers Company, Division Of Conopco, Inc. Production of detergent granulates
US6133223A (en) * 1997-06-27 2000-10-17 Lever Brothers Company, Division Of Conopco, Inc. Production of detergent granulates
ITMI20130757A1 (it) * 2013-05-09 2014-11-10 Unicalce S P A Composizione granulare a ridotta segregabilita', suo procedimento di preparazione e relativi usi

Also Published As

Publication number Publication date
ES2083281T3 (es) 1996-04-01
ATE133447T1 (de) 1996-02-15
DE4209435A1 (de) 1993-09-30
EP0633923A1 (fr) 1995-01-18
TR26864A (tr) 1994-08-19
EP0633923B1 (fr) 1996-01-24
DE59301514D1 (de) 1996-03-07

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