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WO2000071654A1 - Procede de preparation de granulat de tensio-actifs - Google Patents

Procede de preparation de granulat de tensio-actifs Download PDF

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Publication number
WO2000071654A1
WO2000071654A1 PCT/EP2000/004327 EP0004327W WO0071654A1 WO 2000071654 A1 WO2000071654 A1 WO 2000071654A1 EP 0004327 W EP0004327 W EP 0004327W WO 0071654 A1 WO0071654 A1 WO 0071654A1
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WO
WIPO (PCT)
Prior art keywords
granules
carbon atoms
acid
surfactants
surfactant
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PCT/EP2000/004327
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German (de)
English (en)
Inventor
Andreas Lietzmann
Georg Assmann
Wilfried Rähse
Kathleen Paatz
Markus Semrau
Mario Sturm
Original Assignee
Henkel Kommanditgesellschaft Auf Aktien
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Publication of WO2000071654A1 publication Critical patent/WO2000071654A1/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
    • 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
    • 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
    • C11D1/662—Carbohydrates or derivatives
    • 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
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets

Definitions

  • the present invention relates to a process for the production of surfactant granules containing nonionic surfactants, in which the granules are produced by a two-stage process.
  • Compacted or highly concentrated detergent powders or tablets represent a significant proportion of the commercially available detergents and cleaning agents. These agents are generally not obtained by a spray drying process, but rather by mixing, granulating and compacting processes in which high temperatures are avoided. Because of the relatively low temperatures, the removal of water which is introduced by the starting substances is relatively lengthy. A subsequent drying step is often necessary after the granulation has been completed.
  • alkyl polyglycosides are incorporated into the granules.
  • the incorporation of the alkyl polyglycosides is problematic, however, since they cannot be processed by spray drying processes and the resulting particles have a high level of stickiness.
  • the use of alkyl polyglycosides as a paste in the granulation also leads to strongly sticky products, in particular in the case of granules with a high proportion of alkyl benzene sulfonate.
  • the processed polyglycoside pastes Due to their manufacturing process, the processed polyglycoside pastes have a water content of approx. 50% by weight. To produce dry, ie non-sticky, and dust-free granules, it is therefore necessary to remove the water almost completely. The removal of water often leads to granules with fluctuating water content. In particular, if the granules are to be further processed into tablets which must have a quick and constant water solubility, the use of granulated precursors with fluctuating water content can lead to tablets with inconsistent dissolution rates.
  • EP-A-0 859 048 describes a process for producing surfactant granules with bulk densities above 600 g / l by granulating a surfactant preparation, in which solutions of alkylbenzenesulfonate and / or alkylpolyglycoside surfactants and carrier materials in a non- surfactant solvent is simultaneously sprayed through one and the same nozzle and dried in conventional dryers, preferably in the fluidized bed or in a ring mixer dryer.
  • Polycarboxylates and inorganic carriers, in particular amorphous silicates are used as carrier materials.
  • International patent application WO 97/09415 discloses a production process for a non-spray-dried particulate surfactant composition which has a bulk density of at least 600 g / l and contains a polymeric builder component and / or a soil release polymer.
  • the granulating liquid and solid components are mixed in a granulator and the polymer is added in a mixture with a non-aqueous diluent during the granulation step.
  • An ethoxylated nonionic surfactant is preferably used as the non-aqueous diluent.
  • International patent application WO 97/02338 discloses a process for the production of particulate surfactant compositions with a bulk density below 700 g / l.
  • a particulate starting material which has at least 10% by weight of a component with a bulk density of not more than 600 g / l and which is not a surfactant compound is first mixed with a liquid binder in a granulator and then granulated.
  • the particulate starting material contains a builder.
  • Surfactant or a precursor thereof is contained in the particulate starting material and / or in the binder.
  • European patent application 0 799 884 describes a process for producing alkyl polyglycosides containing free-flowing particulate surfactant compositions, according to which a final drying step should not be necessary.
  • a mixture of an aqueous alkylpolyglycoside paste, an ethoxylated nonionic surfactant and a solid water-soluble inorganic salt is first prepared.
  • the mixture obtained separates into an organic phase and a water-rich phase, the organic phase containing alkyl polyglycoside, ethoxylated nonionic surfactant and water being separated off.
  • the proportion of the individual components in the first step is selected so that in the organic phase the ratio of alkyl polyglycoside to ethoxylated nonionic surfactant within the range from 35:65 to 65:35 and the ratio of ethoxylated nonionic surfactant to the total amount of water within the range from 90: 10 to 60: 10 lies.
  • the mixture obtained and optionally further surfactants are mixed with one or more particulate carrier materials and in a conventional manner High speed mixer or granulator processed into a particulate product.
  • the object of the present invention was to provide a process for the production of surfactant granules which does not have the disadvantages mentioned above.
  • a method should be found that leads to granules with a good and constant solubility.
  • granules should be obtained which show such a flowability that no further drying step is required.
  • the present invention accordingly relates to a process for the production of surfactant granules containing nonionic surfactants and further detergent components, in which
  • sugar surfactants are processed into a compound in the presence of water-soluble carrier materials and
  • the compounds obtained in A are mixed with a non-aqueous solvent and the mixture, and optionally further detergent constituents, are granulated in a manner known per se.
  • sugar surfactants which can be used in process step A are the alkyl and alkenyl oliglycosides and polyhydroxy fatty acid amides.
  • alkyl and alkenyl oliglycosides have the general formula R 1 O (G) x (I)
  • R 1 is a primary straight-chain or methyl-branched, in particular in the 2-position methyl-branched alkyl or alkenyl radical having 8 to 22, preferably 12 to 18, carbon atoms and G is the symbol which represents a glycose unit having 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; x is preferably 1.2 to 1.4.
  • Polyhydroxy fatty acid amides which can be used are those having the formula (II).
  • R 2 CO for an aliphatic acyl radical having 6 to 22 carbon atoms
  • R 3 for hydrogen, an alkyl or hydroxyalkyl radical with 1 to 4 carbon atoms
  • [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 92/06984.
  • the polyhydroxy fatty acid amides are preferably derived from reducing sugars with 5 or 6 carbon atoms, in particular from glucose.
  • the sugar surfactants can be used in the form of aqueous solutions as obtained from the manufacturing process.
  • Other forms of use are granules, the production process of which is described in WO97 / 03165, or steam-dried products that can be obtained according to the method described in WO95 / 14519.
  • the carrier materials used in the first process step are preferably water glass or water-soluble detergent builders, such as. B. layered silicates or organic polymers.
  • Amorphous sodium silicates with a Na 2 O: SiO 2 modulus of 1: 2 to 1: 3.3, preferably 1: 2 to 1: 2.8 and in particular 1: 2 to 1: 2.6, are suitable as water glasses call.
  • the delay in dissolution compared to conventional amorphous sodium silicates can be caused in various ways, for example by surface treatment, compounding, compacting / compression or by overdrying.
  • the term “amorphous” is also understood to mean “X-ray amorphous”.
  • silicates in X-ray diffraction experiments do not provide sharp X-ray reflections, as are typical for crystalline substances, but at most one or more maxima of the scattered X-rays, which have a width of several degree units of the diffraction angle.
  • it can very well lead to particularly good builder properties if the silicate particles deliver washed-out or even sharp diffraction maxima in electron diffraction experiments. This is to be interpreted as meaning that the products have microcrystalline areas of size 10 to a few hundred nm, values up to max. 50 nm and in particular up to max. 20 nm are preferred.
  • Such so-called X-ray amorphous silicates which also have a delay in dissolution compared to conventional water glasses, are described, for example, in German patent application DE-A-44 00 024. Compacted / compacted amorphous silicates, compounded amorphous silicates and over-dried X-ray amorphous silicates are particularly preferred.
  • Suitable crystalline, layered sodium silicates have the general formula NaMS O ⁇ H 2 O, where M is sodium or hydrogen, x is a number from 1, 9 to 4 and y is a number from 0 to 20 and preferred values for x 2, 3 or 4 are.
  • Such crystalline layered silicates are described, for example, in European patent application EP-A-0 164 514.
  • Preferred crystalline layered silicates of the formula given are those in which M represents sodium and x assumes the values 2 or 3.
  • both ⁇ - and ⁇ -sodium disilicates Na 2 Si 2 O 5 yH 2 O are preferred, with ⁇ -sodium disilicate can be obtained, for example, by the method described in international patent application WO-A-91/08171.
  • Usable organic carrier materials are, for example, the polycarboxylic acids which can be used in the form of their sodium salts, polycarboxylic acids being understood to mean those carboxylic acids which carry more than one acid function.
  • these are citric acid, adipic acid, succinic acid, glutaric acid, malic acid, tartaric acid, maleic acid, fumaric acid, sugar acids, aminocarboxylic acids, nitrilotriacetic acid (NTA), as long as such use is not objectionable for ecological reasons, and mixtures of these.
  • 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.
  • the acids themselves can also be used.
  • the acids typically also have the property of an acidifying component and thus also serve to set a lower and milder pH value for detergents or cleaning agents.
  • Citric acid, succinic acid, glutaric acid, adipic acid, gluconic acid and any mixtures thereof can be mentioned in particular.
  • Polymeric polycarboxylates are also suitable as builders, for example the alkali metal salts of polyacrylic acid or polymethacrylic acid, for example those with a relative molecular weight of 500 to 70,000 g / mol.
  • the molecular weights given for polymeric polycarboxylates are weight-average molecular weights M w of the particular acid form, which were determined in principle by means of gel permeation chromatography (GPC), using a UV detector. The measurement was made against an external polyacrylic acid standard, which provides realistic molecular weight values due to its structural relationship to the polymers investigated. This information differs significantly from the molecular weight information for which polystyrene sulfonic acids are used as standard. The molecular weights measured against polystyrene sulfonic acids are generally significantly higher than the molecular weights given in this document.
  • Suitable polymers are, in particular, polyacrylates, which preferably have a molecular weight of 2,000 to 20,000 g / mol. Because of their superior solubility, the short-chain polyacrylates which have molar masses from 2000 to 10000 g / mol, and particularly preferably from 3000 to 5000 g / mol, can in turn be preferred from this group.
  • copolymeric polycarboxylates 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 2,000 to 70,000 g / mol, preferably 20,000 to 50,000 g / mol and in particular 30,000 to 40,000 g / mol.
  • the (co) polymeric polycarboxylates can be used either as a powder or as an aqueous solution.
  • the content of (co) polymeric polycarboxylates in the agents is preferably 0.5 to 20% by weight, in particular 3 to 10% by weight.
  • the polymers can also contain allylsulfonic acids, such as, for example, in EP-B-727448 allyloxybenzenesulfonic acid and methallylsulfonic acid, as a monomer.
  • biodegradable polymers composed of more than two different monomer units, for example those which, according to DE-A-43 00 772, are salts of acrylic acid and maleic acid as well as vinyl alcohol or vinyl alcohol derivatives or according to DE-C -42 21 381 contain as monomers salts of acrylic acid and 2-alkylallylsulfonic acid as well as sugar derivatives.
  • copolymers are those which are described in German patent applications DE-A-43 03 320 and DE-A-44 17 734 and preferably contain acrolein and acrylic acid / acrylic acid salts or acrolein and vinyl acetate as monomers.
  • Suitable organic builder substances are dextrins, for example oligomers or polymers of carbohydrates, which are obtained by partial hydrolysis of starches can be.
  • the hydrolysis can be carried out by customary processes, for example acid-catalyzed or enzyme-catalyzed. They are preferably hydrolysis products with average molar masses in the range from 400 to 500,000 g / mol.
  • DE dextrose equivalent
  • the oxidized derivatives of such dextrins are their reaction products with oxidizing agents, which are capable of oxidizing at least one alcohol function of the saccharide ring to the carboxylic acid function.
  • oxidizing agents capable of oxidizing at least one alcohol function of the saccharide ring to the carboxylic acid function.
  • Such oxidized dextrins and processes for their preparation are known, for example, from European patent applications EP-A-0 232 202, EP-A-0 427 349, EP-A-0 472 042 and EP-A-0 542 496 as well as international patent applications WO 92 / 18542, WO 93/08251, WO 93/16110, WO 94/28030, WO 95/07303, WO 95/12619 and WO 95/20608.
  • An oxidized oligosaccharide according to German patent application DE-A-196 00 018 is also suitable.
  • a product oxidized at C 6 of the saccharide ring can
  • Ethylenediamine N, N'-disuccinate (EDDS) whose synthesis is described for example in US 3,158,615, preferably in the form of its sodium or magnesium salts.
  • glycerol disuccinates and glycerol trisuccinates as described, for example, in US Pat. Nos. 4,524,009, 4,639,325, European Patent Application EP-A-0 150 930 and Japanese Patent Application JP 93/339896 become.
  • Suitable amounts for use in formulations containing zeolite and / or silicate are 3 to 15% by weight.
  • organic cobuilders are, for example, acetylated hydroxycarboxylic acids or their salts, which may also be in lactone form and which contain at least 4 carbon atoms and at least one hydroxyl group and a maximum of two acid groups.
  • Such cobuilders are described, for example, in international patent application WO 95/20029.
  • Suitable carrier materials are oxidation products of carboxyl group-containing polyglucosans and / or their water-soluble salts, as are described, for example, in international patent application WO-A-93/08251 or whose preparation is described, for example, in international patent application WO-A-93/16110 .
  • Oxidized oligosaccharides according to German patent application DE 196 00 018 are also suitable.
  • polymeric aminodicarboxylic acids their salts or their precursor substances.
  • Particularly preferred are polyaspartic acids or their salts and derivatives, of which it is disclosed in German patent application DE-A-195 40 086 that in addition to cobuilder properties they also have a bleach-stabilizing effect.
  • polyacetals which can be obtained by reacting dialdehydes with polyolcarboxylic acids which have 5 to 7 carbon atoms and at least 3 hydroxyl groups, for example as described in European patent application EP-A-0 280 223.
  • Preferred polyacetals are obtained from dialdehydes such as glyoxal, glutaraldehyde, terephthalaldehyde and their mixtures and from polyol carboxylic acids such as gluconic acid and / or glucoheptonic acid.
  • phosphonates are, in particular, hydroxyalkane or aminoalkane phosphonates.
  • hydroxyalkane phosphonates 1-hydroxyethane-1,1-diphosphonate (HEDP) is of particular importance as a cobuilder. It is preferably used as the sodium salt, the disodium salt reacting neutrally and the tetrasodium salt in an alkaline manner (pH 9).
  • Preferred aminoalkane phosphonates are ethylenediamine tetramethylene phosphonate (EDTMP), diethylene triamine pentamethylene phosphonate (DTPMP) and their higher homologs.
  • HEDP is preferably used as the builder from the class of the phosphonates.
  • the aminoalkanephosphonates also have a pronounced ability to bind heavy metals. Accordingly, it may be preferred, particularly if the agents also contain bleach, to use aminoalkanephosphonates, in particular DTPMP, or to use mixtures of the phosphonates mentioned.
  • the first process step A compounds with a particle size of preferably at most 1 mm, in particular of at most 0.8 mm and in particular of at most 0.4 mm are obtained. If coarser particles are formed, they can be ground in a mill downstream of the first process step and brought to the desired particle size.
  • the first process step is preferably carried out in a conventional fluidized bed granulation and / or steam drying system.
  • the compounds obtained in the first step A are mixed with a non-aqueous solvent, the mixture and optionally further detergent components are granulated in a manner known per se.
  • Those compounds which are liquid at a temperature of about 80 ° C., preferably at 40 ° C. and particularly preferably at room temperature and which additionally have washing-active properties are preferably used as non-aqueous solvents.
  • Liquid nonionic surfactants are particularly preferably used.
  • the liquid nonionic surfactant preferably used as solvent in step B is preferably a fatty alcohol alkoxylate.
  • Alkoxylated, advantageously ethoxylated, in particular primary alcohols with 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 linear are particularly suitable and may contain methyl-branched radicals in the mixture, as are usually present in oxo alcohol radicals.
  • alcohol ethoxylates with linear residues of alcohols of native origin with 12 to 18 carbon atoms for example from coconut, palm, tallow or oleyl alcohol, and an average of 2 to 8 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, Cg-C ⁇ alcohols 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 alcohols with 7EO.
  • the degrees of ethoxylation given represent statistical averages, which can be an integer or a fraction for a specific product.
  • Preferred alcohol ethoxylates have a narrow homolog distribution (narrow range ethoxylates, NRE).
  • fatty alcohols with more than 12 EO can also be used. Examples of these are (tallow) fatty alcohols with 14 EO, 16 EO, 20 EO, 25 EO, 30 EO or 40 EO.
  • the granulation can be carried out in a large number of apparatuses customarily used in the detergent and cleaning agent industry. For example, it is possible to use the rounding agents commonly used in pharmacy. In such turntable devices, the residence time of the granules is usually less than 20 seconds.
  • Conventional mixers and mixing granulators are also suitable for granulation. Both high-intensity mixers (“high-shear mixers”) and normal mixers with lower circulation speeds can be used as mixers.
  • Suitable mixers are, for example, EirichO mixers of the R or RV series (trademark of Maschinenfabrik Gustav Eirich, Hardheim), Schugi® Flexomix, the Fukae® FS-G mixer (trademark of Fukae Powtech, Kogyo Co., Japan), the Lödige ® FM, KM and CB mixer (trademark of Lödige Maschinenbau GmbH, Paderborn) or the Drais® series T or KT (trademark of Drais-Werke GmbH, Mannheim).
  • the particles are granulated by liquid bonding of the non-aqueous binders.
  • the Residence times of the granules in the mixers are in the range of less than 60 seconds, the residence time also depending on the speed of rotation of the mixer. The dwell times are reduced accordingly the faster the mixer runs.
  • the residence times of the granules in the mixer / rounder are preferably less than one minute, preferably less than 15 seconds. Dwell times of up to 20 minutes are set in slow-running mixers, for example a Lödige KM, dwell times below 10 minutes being preferred because of the process economy.
  • the surfactant-containing granules are compressed under pressure and under the action of shear forces, homogenized in the process and then discharged from the apparatus in a shaping manner.
  • the most technically significant press agglomeration processes are extrusion, roller compacting, pelleting and tableting.
  • preferred press agglomeration processes used to produce the surfactant-containing granules are extrusion, roller compacting and pelletizing.
  • the granules obtained can be powdered with an oil absorption component in order to further improve their processability and meterability.
  • This final powdering step with a finely divided component binds the liquids to the surface of the granules so that the granules cannot clump together during storage.
  • the oil absorption component should have an oil absorption capacity of at least 20g / 100g, more preferably at least 50g / 100g, preferably at least 80g / 100g, particularly preferably at least 120g / 100g and in particular at least 140g / 100g.
  • the oil absorption capacity is a physical property of a substance that can be determined using standardized methods. For example, the British standard methods BS1795 and BS3483: Part -37: 1982 exist, both of which refer to the ISO 787/5 standard.
  • a balanced sample of the substance in question is placed on a plate and refined linseed oil (density: 0.93) "3" is added dropwise from a burette. After each addition, the powder is mixed with the oil Use a spatula mixed vigorously, adding oil until a paste of smooth consistency is obtained. This paste should flow or run without crumbling.
  • the oil absorption capacity is now the amount of the added oil, based on 100g absorbent and is given in ml / 100g or g / 100g, whereby conversions about the density of the linseed oil are possible without any problems.
  • the oil absorption component preferably has the smallest possible average particle size, since the active surface increases with decreasing particle size.
  • Preferred detergent tablets contain a component with an oil absorption capacity of at least 20 g / 100 g, which has an average particle size of less than 50 ⁇ m, preferably less than 20 ⁇ m and in particular less than 10 ⁇ m.
  • a large number of substances are suitable as an oil absorption component.
  • inorganic and organic substances which have a large oil absorption capacity.
  • examples include finely divided substances that are obtained by precipitation.
  • silicates, aluminosilicates, calcium silicates, magnesium silicates and calcium carbonate are used as substances.
  • Diatomaceous earth (diatomaceous earth) and finely divided cellulose fibers or derivatives thereof can also be used in the context of the present invention.
  • Preferred detergent tablets are characterized in that the component contained in them with an oil absorption capacity of at least 20 g / 100 g is selected from silicates and / or aluminosilicates, in particular from the group of silicas and / or zeolites.
  • finely divided zeolites can be used, but also pyrogenic silicas (Aerosil ® ) or silicas that have been obtained by precipitation.
  • surfactants in particular anionic surfactants, and builder substances can be incorporated into the surfactant granules as further constituents.
  • the further constituents are incorporated in the second process step as spray-dried powder.
  • Temperature-sensitive or water-sensitive components can be added separately. All builders suitable for detergents and cleaning agents which have a sufficiently large inner surface area to be able to take up the nonionic surfactant can be used as builders. Examples of these are zeolites, amorphous silicates, soda, phosphates and mixtures thereof, zeolite being preferred.
  • zeolite for example, finely crystalline, synthetic and bound water-containing zeolite such as zeolite A, zeolite P and mixtures of A and P can be used.
  • Zeolite MAP® commercial product from Crosfield
  • zeolite P may be mentioned, for example, as commercially available zeolite P.
  • Zeolites of the faujasite type may be mentioned as further preferred and particularly suitable zeolites.
  • the mineral faujasite belongs to the faujasite types within the zeolite structure group 4, which is characterized by the double six-ring subunit D6R (compare Donald W. Breck: "Zeolite Molecular Sieves", John Wiley & Sons , New York, London, Sydney, Toronto, 1974, page 92).
  • the zeolite structure group 4 also includes the minerals chabazite and gmelinite and the synthetic zeolites R (chabazite type), S (gmelinite type), L and ZK-5. The latter two synthetic zeolites have no mineral analogues.
  • Faujasite-type zeolites are made up of ß-cages, which are linked tetrahedrally via D6R subunits, the ß-cages being arranged in a diamond similar to the carbon atoms.
  • the three-dimensional network of the faujasite-type zeolites used in the process according to the invention has pores of 2.2 and 7.4 ⁇ , the unit cell also contains 8 cavities with a diameter of approximately 13 ⁇ and can be determined using the formula Na 86 [(AIO 2 ) 86 (SiO 2 ) 106 ] ⁇ 264 H 2 O describe.
  • the network of zeolite X contains a void volume of approximately 50%, based on the dehydrated crystal, which represents the largest empty space of all known zeolites (zeolite Y: approx. 48% void volume, faujasite: approx. 47% void volume).
  • zeolite Y approx. 48% void volume
  • faujasite approx. 47% void volume.
  • zeolite of the faujasite type denotes all three zeolites which form the faujasite subgroup of the zeolite structure group 4.
  • zeolite Y and faujasite and mixtures of these compounds can also be used according to the invention, pure zeolite X being preferred.
  • Mixtures or cocrystals of zeolites of the faujasite type with other zeolites which do not necessarily have to belong to the zeolite structural group 4 can also be used according to the invention, the advantages of the process according to the invention becoming particularly evident when at least 50 % By weight of the zeolites are faujasite-type zeolites.
  • the aluminum silicates which are used in the process according to the invention are commercially available and the methods for their preparation are described in standard monographs.
  • x can have values between 0 and 276 and the pore sizes range from 8.0 to 8.4 ⁇ .
  • zeolite X and zeolite A (ca. 80 wt .-% zeolite X) which is marketed by CONDEA Augusta SpA under the trade name VEGO-BOND AX ® is distributed and by the formula
  • Y-type zeolites are also commercially available and can be expressed, for example, by the formulas
  • x stands for numbers between 0 and 276 and have a pore size of 8.0 ⁇ .
  • the particle sizes of the zeolites of the Fauja-sit type used in the process according to the invention are in the range from 0.1 to 100 ⁇ m, preferably between 0.5 and 50 ⁇ m and in particular between 1 and 30 ⁇ m, in each case using standard particle size determination methods measured.
  • the agents according to the invention can also contain anionic surfactants, such as C 8 -C 22 alkyl sulfates, C 8 -C 22 alkanesulfonates, C 8 -C 22 olefin sulfonates, C 8 -C 22 alkylbenzenesulfonates, C 8 -C 22 fatty acid ether sulfates, C 8 -C 22 fatty acid ester sulfonates, sulfated fatty acid glycerol esters, 2,3-C 8 -C 22 alkyl sulfates, salts, monoesters and / or diesters of alkyl sulfosuccinic acid (sulfosuccinates), sulfuric acid monoesters with 1 to 6 moles of ethylene oxide ethoxylated straight-chain or branched C 7 -C 21 alcohols, fatty acid soaps or mixtures thereof.
  • anionic surfactants such as C 8 -C 22 alky
  • the agents according to the invention can contain all substances usually contained in washing and cleaning agents, such as inorganic salts, bleaching agents, bleach activators, graying inhibitors, foam inhibitors, salts of polyphosphonic acids, optical brighteners, enzymes or mixtures thereof.
  • the granules produced according to the invention can either be used as the sole detergent component or can be mixed and packaged with other particles which contain further detergent components. In a preferred embodiment, the granules are mixed with further detergent components and pressed into detergent tablets.
  • a sugar surfactant compound to that shown in Table 1 in a Wirbei fürgranulationsstrom was by spraying a 50% alkylpolyglycoside paste in the first step and ® a 40% Sokalan solution (acrylic acid-maleic acid Copoiymer, commercial product from. BASF AG, Ludwigshafen). The product obtained was then ground in a mortar mill to a maximum particle size of 0.1 mm.
  • Comparative Example 1 the powders were granulated with a mixture of nonionic surfactant and glycerol; in Comparative Example 2, only nonionic surfactant was used.
  • the granules obtained were sieved between 0.6 and 1.6 mm.
  • the proportion of the granules which has a particle size between 0.6 and 1.6 mm is referred to as good grain in Table 4. It was not necessary to dry the granules obtained.

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Abstract

Procédé de préparation de granulat de tensio-actifs, contenant des tensio-actifs non ioniques, qui consiste (A) à travailler dans une première étape des tensio-actifs glucidiques en présence de matières de support hydrosolubles pour obtenir un composé et (B) à mélanger les composés obtenus lors de l'étape (A) avec un solvant non aqueux, puis à granuler de manière connue ledit mélange, ainsi que d'éventuels autres constituants de détergent. Le granulat obtenu possède une bonne solubilité et des propriétés d'écoulement telles qu'il est possible de renoncer à une étape finale de séchage.
PCT/EP2000/004327 1999-05-22 2000-05-13 Procede de preparation de granulat de tensio-actifs WO2000071654A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19923626.7 1999-05-22
DE1999123626 DE19923626A1 (de) 1999-05-22 1999-05-22 Verfahren zur Herstellung von Tensidgranulaten

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WO2000071654A1 true WO2000071654A1 (fr) 2000-11-30

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Families Citing this family (3)

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Publication number Priority date Publication date Assignee Title
GB0111863D0 (en) 2001-05-15 2001-07-04 Unilever Plc Granular composition
GB0111862D0 (en) 2001-05-15 2001-07-04 Unilever Plc Granular composition
CN105602773B (zh) * 2016-02-17 2018-08-03 茗燕生物科技(上海)有限公司 洗衣片智能化生产系统

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04356599A (ja) * 1991-06-03 1992-12-10 Kao Corp アルキルグリコシド含有粒子及びその製造方法
DE4216775A1 (de) * 1992-05-21 1993-11-25 Henkel Kgaa Pulverförmige Tensidmischung
EP0694608A1 (fr) * 1994-07-28 1996-01-31 The Procter & Gamble Company Procédé pour la fabrication de détergents granulations et compositions détergents à base de surface non ionique
WO1997003165A1 (fr) * 1995-07-10 1997-01-30 Henkel Kommanditgesellschaft Auf Aktien Procede de preparation de granules tensioactifs de saccharose
EP0799884A2 (fr) * 1996-04-02 1997-10-08 Unilever Plc Mélanges de tensioactifs, procédés pour leur préparation et composition détergentes sous forme de particules les contenant
EP0814152A2 (fr) * 1996-06-19 1997-12-29 Henkel Kommanditgesellschaft auf Aktien Procédé de préparation des détergents solides
EP0859048A2 (fr) * 1997-01-27 1998-08-19 Henkel Kommanditgesellschaft auf Aktien Procédé pour la fabrication de granules tensioactifs
EP0897976A2 (fr) * 1997-07-04 1999-02-24 Henkel Kommanditgesellschaft auf Aktien Masse volumique de détergent granulaire à grande solubilité et à pouvoir perfectionné pour laver les graisses

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04356599A (ja) * 1991-06-03 1992-12-10 Kao Corp アルキルグリコシド含有粒子及びその製造方法
DE4216775A1 (de) * 1992-05-21 1993-11-25 Henkel Kgaa Pulverförmige Tensidmischung
EP0694608A1 (fr) * 1994-07-28 1996-01-31 The Procter & Gamble Company Procédé pour la fabrication de détergents granulations et compositions détergents à base de surface non ionique
WO1997003165A1 (fr) * 1995-07-10 1997-01-30 Henkel Kommanditgesellschaft Auf Aktien Procede de preparation de granules tensioactifs de saccharose
EP0799884A2 (fr) * 1996-04-02 1997-10-08 Unilever Plc Mélanges de tensioactifs, procédés pour leur préparation et composition détergentes sous forme de particules les contenant
EP0814152A2 (fr) * 1996-06-19 1997-12-29 Henkel Kommanditgesellschaft auf Aktien Procédé de préparation des détergents solides
EP0859048A2 (fr) * 1997-01-27 1998-08-19 Henkel Kommanditgesellschaft auf Aktien Procédé pour la fabrication de granules tensioactifs
EP0897976A2 (fr) * 1997-07-04 1999-02-24 Henkel Kommanditgesellschaft auf Aktien Masse volumique de détergent granulaire à grande solubilité et à pouvoir perfectionné pour laver les graisses

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 199304, Derwent World Patents Index; Class D25, AN 1993-030610, XP002144604 *

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CA2308910A1 (fr) 2000-11-22

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