EP1005522B1 - Procede de production d'une composition detergente de faible densite par commande de la hauteur de la buse d'un sechoir a lit fluide - Google Patents

Procede de production d'une composition detergente de faible densite par commande de la hauteur de la buse d'un sechoir a lit fluide Download PDF

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EP1005522B1
EP1005522B1 EP98935559A EP98935559A EP1005522B1 EP 1005522 B1 EP1005522 B1 EP 1005522B1 EP 98935559 A EP98935559 A EP 98935559A EP 98935559 A EP98935559 A EP 98935559A EP 1005522 B1 EP1005522 B1 EP 1005522B1
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Prior art keywords
agglomerates
detergent
fluid bed
bed dryer
binder
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German (de)
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EP1005522A1 (fr
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Allen Dale Beer
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Procter and Gamble Co
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Procter and Gamble Co
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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • 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
    • 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
    • C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets

Definitions

  • the present invention generally relates to a process for producing a low density detergent composition. More particularly, the invention is directed to a process during which low density detergent agglomerates are produced by feeding a surfactant paste or liquid acid precursor of anionic surfactant and dry starting detergent material sequentially into two high speed mixers followed by a fluid bed dryer which has an optimally selected nozzle height for spraying on a binder.
  • the process produces a free flowing, low density detergent composition which can be commercially sold as a conventional non-compact detergent composition or used as an admix in a low dosage, "compact" detergent product.
  • the first type of process involves spray-drying an aqueous detergent slurry in a spray-drying tower to produce highly porous detergent granules.
  • the various detergent components are dry mixed after which they are agglomerated with a binder such as a nonionic or anionic surfactant.
  • a binder such as a nonionic or anionic surfactant.
  • the most important factors which govern the density of the resulting detergent granules are the density, porosity and surface area, shape of the various starting materials and their respective chemical composition. These parameters, however, can only be varied within a limited range. Thus, flexibility in the substantial bulk density can only be achieved by additional processing steps which lead to lower density of the detergent granules.
  • WO97/22685 relates to a process for producing a detergent composition involving partial granulation in a high or low shear granulator followed by granulation in a very low shear mixer such as a fluid bed.
  • GB2209172 relates a process for producing a detergent composition involving spraying a liquid component onto a fluidised particulate material in a fluid bed.
  • the present invention meets the aforementioned needs in the art by providing a process which produces a low density (300 - 550 g/l) detergent composition directly from a surfactant paste and dry starting detergent ingredients.
  • the process involves agglomerating the starting detergent ingredients in a high speed mixer followed by a second high speed mixer. Thereafter, the agglomerates formed in the high speed mixers are agglomerated and dried in a fluid bed dryer in which a liquid binder is sprayed onto the agglomerates from one or more nozzles at a selected height from the distribution plate of the fluid bed dryer.
  • the process does not use the conventional spray drying towers currently used and is therefore more efficient, economical and flexible with regard to the variety of detergent compositions which can be produced in the process.
  • the process is more amenable to environmental concerns in that it does not use spray drying towers which typically emit particulates and volatile organic compounds into the atmosphere.
  • agglomerates refers to particles formed by agglomerating detergent granules or particles which typically have a smaller median particle size than the formed agglomerates.
  • median particle size it is meant the particle size diameter value above which 50% of the particles have a larger particle size and below which 50% of particles have a smaller particle size. All percentages used herein are expressed as “percent-by-weight" on an anhydrous basis unless indicated otherwise.
  • a process for preparing low density detergent agglomerates comprises the steps of: (a) agglomerating a detergent surfactant paste or precursor thereof and dry starting detergent material in a first high speed mixer to obtain agglomerates; (b) mixing the agglomerates in a second high speed mixer to obtain built-up agglomerates; and (c) feeding the built-up agglomerates into a fluid bed dryer in which a binder is sprayed via a nozzle having a height of from 25 cm to 60 cm from the distributor plate of the fluid bed dryer such that the built-up agglomerates are dried and agglomerated to form the low detergent agglomerates having a density in a range from 300 g/l to 550 g/l.
  • another process for preparing low density detergent agglomerates comprises the steps of: (a) agglomerating a detergent surfactant paste or precursor thereof and dry starting detergent material in a first high speed mixer to obtain agglomerates; (b) mixing the agglomerates in a second high speed mixer to obtain built-up agglomerates; and (c) feeding the built-up agglomerates into a fluid bed dryer in which sodium silicate is sprayed via a nozzle having a height of from 40 cm to 60 cm from the distributor plate of the fluid bed dryer such that the built-up agglomerates are dried and agglomerated to form the low detergent agglomerates having a density in a range from 300 g/l to 550 g/l.
  • the detergent products made in accordance with any of the process embodiments described herein are also provided.
  • the present invention is directed to a process in which low density agglomerates are produced by a three step process, the last of which involves a fluid bed dryer containing one or more nozzles positioned at a selected height from the distribution plate of the dryer.
  • the process forms free flowing, low density detergent agglomerates which can be used alone as the detergent product or as an admixture with conventional spray-dried detergent granules and/or high density detergent agglomerates in a final commercial detergent product.
  • the process described herein can be operated continuously or in a batch mode depending upon the particularly desired application.
  • One major advantage of the present process is that it utilizes equipment which can be operated differently from the present process parameters to obtain high density detergent compositions.
  • a single large-scale commercial detergent manufacturing facility can be built to produce high or low density detergent compositions depending upon the local consumer demand and its inevitable fluctuations between compact and non-compact detergent products.
  • a detergent surfactant paste or precursor thereof as set forth in more detail hereinafter and dry starting detergent material is inputted and agglomerated in a high speed mixer.
  • the dry starting material can include only those relatively inexpensive detergent materials typically used in modern granular detergent products.
  • Such ingredients include but are not limited to, builders, fillers, dry surfactants, and flow aides.
  • the builder includes aluminosilicates, crystalline layered silicates, phosphates, carbonates and mixtures thereof which is the essential dry starting detergent ingredient within the scope of the current process.
  • Relatively expensive materials such as Burkeite (Na 2 SO 4 ⁇ Na 2 CO 3 ) and the various silicas are not necessary to achieve the desired low density agglomerates produced by the process. Rather, by selecting the binder and nozzle height through which the binder is sprayed onto the agglomerates in the fluid bed dryer as described in more detail hereinafter, the present process achieves the desired low density. Further, it is preferable to include from 1% to about 40% by weight of undersized detergent particles or "fines" in the first step of the process. This can be conveniently accomplished by screening the detergent particles formed subsequent to the fluid bed dryer to a median particle size range of from about 10 microns to about 150 microns and feeding these "fines" back into the first high speed mixer.
  • the high speed mixer can be any one of a variety of commercially available mixers such as a Lödige CB 30 mixer or similar brand mixer. These types of mixers essentially consist of a horizontal, hollow static cylinder having a centrally mounted rotating shaft around which several shovel and rod-shaped blades are attached which have a tip speed of from about 5 m/s to about 30 m/s, more preferably from about 6 m/s to about 26 m/s.
  • the shaft rotates at a speed of from about 100 rpm to about 2500 rpm, more preferably from about 300 rpm to about 1600 rpm.
  • the mean residence time of the detergent ingredients in the high speed mixer is preferably in range from about 2 seconds to about 45 seconds, and most preferably from about 5 seconds to about 1 5 seconds.
  • This mean residence time is conveniently measured by dividing the weight of the mixer at steady state by throughput (kg/hr) flow.
  • Another suitable mixer is any one of the various Flexomix models available from Schugi (Netherlands) which are vertically positioned high speed mixers. This type of mixer is preferably operated at a Froude Index of from about 13 to about 32. See U.S. Patent 5,149,455 to Jacobs et al (issued September 22, 1992) for a detailed discussion of this well-known Froude Index which is a dimensionless number that can be optimally selected by those skilled in the art.
  • a liquid acid precursor of an anionic surfactant is inputted with the dry starting detergent material which at least includes a neutrahzing agent such as sodium carbonate.
  • the preferred liquid acid surfactant precursor is C 11-18 linear alkylbenzene sulfonate surfactant ("HLAS"), although any acid precursor of an anionic surfactant may be used in the process.
  • a more preferred embodiment involves feeding a liquid acid precursor of C 12-14 linear alkylbenzene sulfonate surfactant with a C 10-18 alkyl ethoxylated sulfate ("AS") surfactant into the first high speed mixer, preferably in a weight ratio of from about 5:1 to about 1:5, and most preferably, in a range of from about 1:1 to about 3:1 (HLAS:AS).
  • AS alkyl ethoxylated sulfate
  • the detergent agglomerates formed in the first step are inputted into a second high speed mixer which can be the same piece of equipment as used in the first step or a different type of high speed mixer.
  • a second high speed mixer can be the same piece of equipment as used in the first step or a different type of high speed mixer.
  • a Lödige CB mixer can be used in the first step while a Schugi mixer is used in the second step.
  • the agglomerates are mixed and built-up further in a controlled fashion.
  • binders include liquid sodium silicate, a liquid acid precursor of an anionic surfactant such as HLAS, nonionic surfactant, polyethylene glycol or mixtures thereof.
  • the built-up agglomerates are inputted into a fluid bed dryer in which the agglomerates are dried and agglomerated to a median particle size of from 300 microns to 700 microns, more preferably from 325 microns to
  • the density of the agglomerates formed is from 300 g/l to 550 g/l, more preferably from 350 g/l to 500 g/l, and even more preferably from 400 g/l to 480 g/l. All of these densities are generally below that of typical detergent compositions formed of dense agglomerates or most typical spray-dried granules.
  • a binder as described previously is preferably added during this step to enhance formation of the desired agglomerates.
  • a particularly preferred binder is liquid sodium silicate in an amount of from about 0.1% to about 20% by weight of the final low density composition.
  • the nozzle height through which the binder is added is from 25 cm to 60 cm, more preferably from 30 cm to 60 cm, most preferably from 40 cm to 60 cm, and even more preferably at 40 cm, from the distribution plate of the fluid bed dryer. Preferably all of the nozzles used in the fluid bed drying apparatus have such a height arrangement. Unexpectedly, it has been found that by selecting the nozzle height to be within the aforementioned ranges, superior low density agglomerates are produced in the process from both a low density and free flowability standpoint.
  • the benefits of the process in this regard can be enhanced by maintaining the spray-on flux of the binder in the fluid bed to be from 0.02 kg/cm 2 /hr to 0.06 kg/cm 2 /hr, more preferably from 0.04 kg/cm 2 /hr to 0.05 kg/cm 2 /hr.
  • the air inlet temperature in the fluid bed dryer is from 100°C to 200°C, more preferably from 110°C to 130°C.
  • the unfluidized bed height in fluid bed dryer is preferably from 5 cm to 20 cm. It has also been found that the process benefits can be enhanced by maintaining the fluidized air flux in the fluid bed dryer is from 0.6 kg/m 2 /s to 0.8 kg/m 2 /s.
  • the liquid silicate can be added at two locations in the fluid bed dryer, e.g., at or near the inlet port and at or near the exit port.
  • the median binder droplet diameter is from 20 microns to 100 microns preferably 20 to 150 microns, a parameter which enhances formation of the desired built-up agglomerates.
  • the ratio of the median binder droplet diameter to built-up agglomerate (exiting the second high speed mixer) particle diameter is preferably from 0.1 to 0.6.
  • the process may involve adding the binder to both the second high speed mixer as well as the fluid bed dryer. It has also been found beneficial to add the binder simultaneously at more than one location in one or more of the steps of the process.
  • the liquid silicate can be added at two locations in the fluid bed dryer, e.g., at or near the inlet port and at or near the exit port.
  • the agglomerates are built-up from smaller sizes to large sized particles having a high degree of intraparticle porosity.
  • the degree of intraparticle porosity is preferably from about 20% to about 40%, and most preferably from about 25% to about 35%.
  • the intraparticle porosity can be conveniently measured by standard mercury porosimetry testing.
  • optional steps contemplated by the present process include screening the oversized detergent agglomerates in a screening apparatus which can take a variety of forms including but not limited to conventional screens chosen for the desired particle size of the finished detergent product.
  • Other optional steps include conditioning of the detergent agglomerates by subjecting the agglomerates to additional drying and/or cooling by way of apparatus discussed previously.
  • Another optional step of the instant process entails finishing the resulting detergent agglomerates by a variety of processes including spraying and/or admixing other conventional detergent ingredients.
  • the finishing step encompasses spraying perfumes, brighteners and enzymes onto the finished agglomerates to provide a more complete detergent composition.
  • Such techniques and ingredients are well known in the art.
  • the liquid acid precursor of anionic surfactant is used in the first step of the process, and in optional embodiments, as a liquid binder in the second and/or third essential steps of the process.
  • This liquid acid precursor will typically have a viscosity measured at 30°C of from about 500 cps to about 5,000 cps.
  • the liquid acid is a precursor for the anionic surfactants described in more detail hereinafter.
  • a detergent surfactant paste can also be used in the process and is preferably in the form of an aqueous viscous paste, although other forms are also contemplated by the invention.
  • This so-called viscous surfactant paste has a viscosity of from about 5,000 cps to about 100,000 cps, more preferably from about 10,000 cps to about 80,000 cps, and contains at least about 10% water, more preferably at least about 20% water. The viscosity is measured at 70°C and at shear rates of about 10 to 100 sec. -1 .
  • the surfactant paste if used, preferably comprises a detersive surfactant in the amounts specified previously and the balance water and other conventional detergent ingredients.
  • the surfactant itself, in the viscous surfactant paste, is preferably selected from anionic, nonionic, zwitterionic, ampholytic and cationic classes and compatible mixtures thereof.
  • Detergent surfactants useful herein are described in U.S. Patent 3,664,961, Norris, issued May 23, 1972, and in U.S. Patent 3,919,678, Laughlin et al., issued December 30, 1975.
  • Useful cationic surfactants also include those described in U.S. Patent 4,222,905, Cockrell, issued September 16, 1980, and in U.S. Patent 4,239,659, Murphy, issued December 16, 1980.
  • anionics and nonionics are preferred and anionics are most preferred.
  • Nonlimiting examples of the preferred anionic surfactants useful in the surfactant paste, or from which the liquid acid precursor described herein derives include the conventional C 11 -C 18 alkyl benzene sulfonates ("LAS"), primary, branched-chain and random C 10 -C 20 alkyl sulfates (“AS”), the C 10 -C 18 secondary (2,3) alkyl sulfates of the formula CH 3 (CH 2 ) x (CHOSO 3 - M + ) CH 3 and CH 3 (CH 2 ) y (CHOSO 3 - M + )CH 2 CH 3 where x and (y + 1) are integers of at least about 7, preferably at least about 9, and M is a 510 water-solubilizing cation, especially sodium, unsaturated sulfates such as oleyl sulfate, and the C 10 -C 18 alkyl alkoxy sulfates ("AE x S"; especially EO 1-7 ethoxy sulfates).
  • exemplary surfactants useful in the paste of the invention include and C 10 -C 18 alkyl alkoxy carboxylates (especially the EO 1-5 ethoxycarboxylates), the C 10-18 glycerol ethers, the C 10 -C 18 alkyl polyglycosides and their corresponding sul fated polyglycosides, and C 12 -C 18 alpha-sulfonated fatty acid esters.
  • the conventional nonionic and amphoteric surfactants such as the C 12 -C 18 alkyl ethoxylates ("AE") including the so-called narrow peaked alkyl ethoxylates and C 6 -C 12 alkyl phenol alkoxylates (especially ethoxylates and mixed ethoxy/propoxy), C 12 -C 18 betaines and sulfobetaines ("sultaines"), C 10 -C 18 amine oxides, and the like, can also be included in the overall compositions.
  • the C 10 -C 18 N-alkyl polyhydroxy fatty acid amides can also be used. Typical examples include the C 12 -C 18 N-methylglucamides. See WO 9,206,154.
  • sugar-derived surfactants include the N-alkoxy polyhydroxy fatty acid amides, such as C 10 -C 18 N-(3-methoxypropyl) glucamide.
  • the N-propyl through N-hexyl C 12 -C 18 glucamides can be used for low sudsing.
  • C 10 -C 20 conventional soaps may also be used. If high sudsing is desired, the branched-chain C 10 -C 16 soaps may be used. Mixtures of anionic and nonionic surfactants are especially useful. Other conventional useful surfactants are listed in standard texts.
  • the starting dry detergent material of the present process preferably comprises a builder and other standard detergent ingredients such as sodium carbonate, especially when a liquid acid precursor of a surfactant is used as it is needed as a neutralizing agent in the first step of the process.
  • preferable starting dry detergent material includes sodium carbonate and a phosphate or an aluminosilicate builder which is referenced as an aluminosilicate ion exchange material.
  • a preferred builder is selected from the group consisting of aluminosilicates, crystalline layered silicates, phosphates, carbonates and mixtures thereof.
  • Preferred phosphate builders include sodium tripolyphosphate, tetrasodium pyrophosphate and mixtures thereof.
  • inorganic phosphate builders are sodium and potassium tripolyphosphate, pyrophosphate, polymeric metaphosphate having a degree of polymerization of from about 6 to 21, and orthophosphates.
  • polyphosphonate builders are the sodium and potassium salts of ethylene diphosphonic acid, the sodium and potassium salts of ethane 1-hydroxy-1, 1-diphosphonic acid and the sodium and potassium salts of ethane, 1,1,2-triphosphonic acid.
  • Other phosphorus builder compounds are disclosed in U.S. Patents 3,159,581; 3,213,030; 3,422,021; 3,422,137; 3,400,176 and 3,400,148.
  • the aluminosilicate ion exchange materials used herein as a detergent builder preferably have both a high calcium ion exchange capacity and a high exchange rate. Without intending to be limited by theory, it is believed that such high calcium ion exchange rate and capacity are a function of several interrelated factors which derive from the method by which the aluminosilicate ion exchange material is produced. In that regard, the aluminosilicate ion exchange materials used herein are preferably produced in accordance with Corkill et al, U.S. Patent No. 4,605,509 (Procter & Gamble).
  • the aiuminosilicate ion exchange material is in "sodium" form since the potassium and hydrogen forms of the instant aluminosilicate do not exhibit the as high of an exchange rate and capacity as provided by the sodium form.
  • the aiuminosilicate ion exchange material preferably is in over dried form so as to facilitate production of crisp detergent agglomerates as described herein.
  • the aluminosilicate ion exchange materials used herein preferably have particle size diameters which optimize their effectiveness as detergent builders.
  • particle size diameter represents the average particle size diameter of a given aluminosilicate ion exchange material as determined by conventional analytical techniques, such as microscopic determination and scanning electron microscope (SEM).
  • the preferred particle size diameter of the aluminosilicate is from about 0.1 micron to about 10 microns, more preferably from about 0.5 microns to about 9 microns. Most preferably, the particle size diameter is from about 1 microns to about 8 microns.
  • the aluminosilicate ion exchange material has the formula Na z [(AlO 2 ) z .(SiO 2 ) y ]xH 2 O wherein z and y are integers of at least 6, the molar ratio of z to y is from about 1 to about 5 and x is from about 10 to about 264. More preferably, the aluminosilicate has the formula Na 12 [(AlO 2 ) 12 .(SiO 2 ) 12 ]xH 2 O wherein x is from about 20 to about 30, preferably about 27.
  • These preferred aluminosilicates are available commercially, for example under designations Zeolite A, Zeolite B and Zeolite X.
  • naturally-occurring or synthetically derived aluminosilicate ion exchange materials suitable for use herein can be made as described in Krummel et al, U.S. Patent No. 3,985,669.
  • aluminosilicates used herein are further characterized by their ion exchange capacity which is at least about 200 mg equivalent of CaCO 3 hardness/gram, calculated on an anhydrous basis, and which is preferably in a range from about 300 to 352 mg equivalent of CaCO 3 hardness/gram.
  • the instant aluminosilicate ion exchange materials are still further characterized by their calcium ion exchange rate which is at least about 0.13g Ca 2+ /L/min/-g/L (2 grains Ca ++ /gallon/minute/-gram/gallon) and more preferably in a range from about 0.13g Ca 2+ /L/min/-g/L (2 grains Ca ++ /gallon/minute/-gram/gallon) to about 0.39g Ca 2+ /L/min/-g/L (6 grains Ca ++ /gallon/minute/-gram/gallon).
  • the starting dry detergent material in the present process can include additional detergent ingredients and/or, any number of additional ingredients can be incorporated in the detergent composition during subsequent steps of the present process.
  • adjunct ingredients include other detergency builders, bleaches, bleach activators, suds boosters or suds suppressors, anti-tarnish and anticorrosion agents, soil suspending agents, soil release agents, germicides, pH adjusting agents, non-builder alkalinity sources, chelating agents, smectite clays, enzymes, enzyme-stabilizing agents and perfumes. See U.S. Patent 3,936.537, issued February 3, 1976 to Baskerville, Jr. et al.,
  • Other builders can be generally selected from the various borates, polyhydroxy sulfonates, polyacetates, carboxylates, citrates, tartrate mono- and di-succinates, and mixtures thereof.
  • Preferred are the alkali metal, especially sodium, salts of the above.
  • crystalline layered sodium silicates exhibit a clearly increased calcium and magnesium ion exchange capacity.
  • the layered sodium silicates prefer magnesium ions over calcium ions, a feature necessary to insure that substantially all of the "hardness" is removed from the wash water.
  • These crystalline layered sodium silicates are generally more expensive than amorphous silicates as well as other builders. Accordingly, in order to provide an economically feasible laundry detergent, the proportion of crystalline layered sodium silicates used must be determined judiciously.
  • the crystalline layered sodium silicates suitable for use herein preferably have the formula NaMSi x O 2x+1 .yH 2 O wherein M is sodium or hydrogen, x is from about 1.9 to about 4 and y is from about 0 to about 20. More preferably, the crystalline layered sodium silicate has the formula NaMSi 2 O 5 .yH 2 O wherein M is sodium or hydrogen, and y is from about 0 to about 20.
  • nonphosphorus, inorganic builders are tetraborate decahydrate and silicates having a weight ratio of SiO 2 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to about 2.4.
  • Water-soluble, nonphosphorus organic builders useful herein include the various alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxy sulfonates.
  • polyacetate and polycarboxylate builders are the sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylene diamine tetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, and citric acid.
  • Polymeric polycarboxylate builders are set forth in U.S. Patent 3,308,067, Diehl, issued March 7, 1967.
  • Such materials include the water-soluble salts of homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid and methylene malonic acid.
  • Some of these materials are useful as the water-soluble anionic polymer as hereinafter described, but only if in intimate admixture with the non-soap anionic surfactant.
  • polycarboxylates for use herein are the polyacetal carboxylates described in U.S. Patent 4,144,226, issued March 13, 1979 to Crutchfield et al, and U.S. Patent 4,246,495, issued March 27, 1979 to Crutchfield et al, both of which are
  • polyacetal carboxylates can be prepared by bringing together under polymerization conditions an ester of glyoxylic acid and a polymerization initiator. The resulting polyacetal carboxylate ester is then attached to chemically stable end groups to stabilize the polyacetal carboxylate against rapid depolymerization in alkaline solution, converted to the corresponding salt, and added to a detergent composition.
  • Particularly preferred polycarboxylate builders are the ether carboxylate builder compositions comprising a combination of tartrate monosuccinate and tartrate disuccinate described in U.S. Patent 4,663,071, Bush et al., issued May 5, 1987.
  • Bleaching agents and activators are described in U.S. Patent 4,412,934, Chung et al., issued November 1, 1983, and in U.S. Patent 4,483,781, Hartman, issued November 20, 1984, both of which are incorporated herein by reference.
  • Chelating agents are also described in U.S. Patent 4,663,071, Bush et al., from Column 17, line 54 through Column 18, line 68, incorporated herein by reference.
  • Suds modifiers are also optional ingredients and are described in U.S. Patents 3,933,672, issued January 20, 1976 to Bartoletta et al., and 4,136,045, issued January 23, 1979 to Gault et al.
  • Suitable smectite clays for use herein are described in U.S. Patent 4,762,645, Tucker et al, issued August 9, 1988, Column 6, line 3 through Column 7, line 24, Suitable additional detergency builders for use herein are enumerated in the Baskerville patent, Column 13, line 54 through Column 16, line 16, and in U.S. Patent 4,663,071, Bush et al, issued May 5, 1987.
  • This Example illustrates the process invention in which a low density agglomerated detergent composition is prepared.
  • a Lödige CB 30 high speed mixer is charged with a mixture of powders, namely sodium carbonate (median particle size 15 microns) and sodium tripolyphosphate ("STPP") with a median particle size of 25 microns.
  • the mixer is operated at 1600 rpm and the sodium carbonate, STPP, HLAS and AES are formed into agglomerates having a median particle size of about 110 microns after a mean residence time in the Lödige CB 30 mixer of about 5 seconds.
  • the agglomerates are then fed to a Schugi (Model # FX160) high speed mixer which is operated at 2800 rpms with a mean residence time of about 2 seconds.
  • a HLAS binder is inputted into the Schugi (Model # FX160) mixer during this step which results in built-up agglomerates having a median particle size of about 180 microns being formed.
  • the built-up agglomerates are passed through a four-zone fluid bed dryer which is operated at an air inlet temperature of about 125°C and a nozzle height of 40 cm from the distribution plate in the first and fourth zones of the fluid bed.
  • fines are also added to the Lödige CB 30 mixer.
  • liquid sodium silicate is fed into the fluid bed dryer resulting in the finished detergent agglomerates having a density of about 485 g/l and a median particle size of about 360 microns.
  • the finished agglomerates have excellent physical properties in that they are free flowing as exhibited by their superior cake strength grades.
  • the agglomerates embody about 14% of fines (less than 150 microns) which are recycled from the fluid bed back into the Lödige CB 30 which enhances production of the agglomerates produced by the process.

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  • Detergent Compositions (AREA)

Claims (10)

  1. Procédé de préparation d'une composition détergente de faible densité, caractérisé par les étapes consistant à :
    (a) agglomérer une pâte tensioactive détergente ou un précurseur acide liquide d'un tensioactif anionique et un matériau détergent de départ sec dans un premier mélangeur à vitesse élevée pour obtenir des agglomérats ;
    (b) mélanger lesdits agglomérats dans un second mélangeur à vitesse élevée pour obtenir des agglomérats composés ; et
    (c) introduire lesdits agglomérats composés dans un sécheur à lit fluidisé dans lequel un liant est pulvérisé par une buse ayant une hauteur de 25 cm à 60 cm à partir du plateau distributeur dudit sécheur à lit fluidisé de manière que lesdits agglomérats composés soient séchés et agglomérés pour former des agglomérats détergents de faible densité ayant une densité dans une plage de 300 g/l à 550 g/l, et une taille particulairé moyenne de 300 µm à 700 µm.
  2. Procédé selon la revendication 1, dans lequel ledit liant est le silicate de sodium.
  3. Procédé selon la revendication 1, dans lequel ledit liant a un flux de pulvérisation de 0,02 kg/cm2/h à 0,06 kg/cm2/h.
  4. Procédé selon la revendication 1, dans lequel la température d'entrée de l'air dudit sécheur à lit fluidisé est de 110°C à 130°C.
  5. Procédé selon la revendication 1, dans lequel ledit liant a un diamètre moyen de gouttelette de 20 microns à 100 microns.
  6. Procédé selon la revendication 1, dans lequel le flux d'air fluidisé dans ledit sécheur à lit fluidisé est de 0,6 kg/m2/s à 0,8 kg/m2/s.
  7. Procédé selon la revendication 1, dans lequel ladite étape (a) comprend l'agglomération d'un précurseur acide liquide de tensioactif alkyl en C11-18 linéaire benzènesulfonate et d'un tensioactif alkyl en C10-18 sulfate éthoxylé.
  8. Procédé selon la revendication 1, dans lequel ledit liant est ajouté aux orifices d'entrée et de sortie dudit sécheur à lit fluidisé.
  9. Procédé selon la revendication 1, dans lequel ladite hauteur de la buse est de 35 cm à 45 cm.
  10. Procédé selon la revendication 1, dans lequel dans l'étape (c) lesdits agglomérats composés sont introduits dans un sécheur à lit fluidisé dans lequel le silicate de sodium est pulvérisé par une buse ayant une hauteur de 40 cm à 60 cm à partir du plateau distributeur dudit sécheur à lit fluidisé.
EP98935559A 1997-07-14 1998-07-08 Procede de production d'une composition detergente de faible densite par commande de la hauteur de la buse d'un sechoir a lit fluide Expired - Lifetime EP1005522B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US5247297P 1997-07-14 1997-07-14
US52472P 1997-07-14
PCT/US1998/014100 WO1999003966A1 (fr) 1997-07-14 1998-07-08 Procede de production d'une composition detergente de faible densite par commande de la hauteur de la buse d'un sechoir a lit fluide

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EP1005522A1 EP1005522A1 (fr) 2000-06-07
EP1005522B1 true EP1005522B1 (fr) 2004-10-06

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EP98935559A Expired - Lifetime EP1005522B1 (fr) 1997-07-14 1998-07-08 Procede de production d'une composition detergente de faible densite par commande de la hauteur de la buse d'un sechoir a lit fluide

Country Status (10)

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EP (1) EP1005522B1 (fr)
JP (1) JP2003521548A (fr)
CN (1) CN1170918C (fr)
AR (1) AR016330A1 (fr)
AT (1) ATE278765T1 (fr)
BR (1) BR9810716A (fr)
CA (1) CA2295941C (fr)
DE (1) DE69826871T2 (fr)
ES (1) ES2230707T3 (fr)
WO (1) WO1999003966A1 (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9526097D0 (en) * 1995-12-20 1996-02-21 Unilever Plc Process
GB9712583D0 (en) 1997-06-16 1997-08-20 Unilever Plc Production of detergent granulates
GB9712580D0 (en) * 1997-06-16 1997-08-20 Unilever Plc Production of detergent granulates
GB9713748D0 (en) * 1997-06-27 1997-09-03 Unilever Plc Production of detergent granulates
DE69904499T2 (de) 1998-10-26 2003-10-30 The Procter & Gamble Company, Cincinnati Verfahren zur herstellung eines granularen waschmittels mit verbessertem aussehen und erhöhter löslichkeit
JP2002533532A (ja) * 1998-12-22 2002-10-08 ザ、プロクター、エンド、ギャンブル、カンパニー 凝集による低かさ密度洗剤組成物の製造方法
GB9913546D0 (en) 1999-06-10 1999-08-11 Unilever Plc Granular detergent component containing zeolite map and laundry detergent compositions containing it
DE10258006B4 (de) * 2002-12-12 2006-05-04 Henkel Kgaa Trockenneutralisationsverfahren II
EP2123742A1 (fr) 2008-05-14 2009-11-25 The Procter and Gamble Company Compositions de détergent solide pour lessive comprenant du sel de silicate à faible densité

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5335568B2 (fr) * 1973-09-10 1978-09-28
GB2209172A (en) * 1987-08-28 1989-05-04 Unilever Plc Preparation of solid particulate components for detergents
GB9526097D0 (en) * 1995-12-20 1996-02-21 Unilever Plc Process

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Publication number Publication date
EP1005522A1 (fr) 2000-06-07
CN1269824A (zh) 2000-10-11
DE69826871D1 (de) 2004-11-11
BR9810716A (pt) 2000-08-08
DE69826871T2 (de) 2006-03-09
CN1170918C (zh) 2004-10-13
WO1999003966A1 (fr) 1999-01-28
JP2003521548A (ja) 2003-07-15
ES2230707T3 (es) 2005-05-01
CA2295941A1 (fr) 1999-01-28
CA2295941C (fr) 2003-04-22
ATE278765T1 (de) 2004-10-15
AR016330A1 (es) 2001-07-04

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