US3598743A - Preparation of granular detergent compositions for automatic dishwashers - Google Patents

Preparation of granular detergent compositions for automatic dishwashers Download PDF

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US3598743A
US3598743A US844191A US3598743DA US3598743A US 3598743 A US3598743 A US 3598743A US 844191 A US844191 A US 844191A US 3598743D A US3598743D A US 3598743DA US 3598743 A US3598743 A US 3598743A
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silicate
granules
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Kenneth Coates
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Procter and Gamble Co
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395Bleaching agents
    • C11D3/3958Bleaching agents combined with phosphates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D11/00Special methods for preparing compositions containing mixtures of detergents
    • C11D11/0082Special 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
    • C11D11/0088Special 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

Definitions

  • Granular dishwashing detergent compositions are prepared by dry-mixing sodium tripolyphosphate and chlorinated trisodium phosphate, spraying aqueous sodium silicate thereon to form agglomerated granules, and cooling by passing cold air at a temperature not exceeding 75 F. through a bed of the granules.
  • This invention relates to the processing of detergent agglomerates comprising sodium tripolyphosphate, chlorinated trisodium phosphate, and sodium silicate. Such agglomerates find wide application in dishwashing, especially in automatic dishwashing machines.
  • a process for preparing a granular detergent composition wherein a particulate mixture of substantially anhydrous sodium tripolyphosphate and chlorinated trisodium phosphate is sprayed with an aqueous solution of sodium silicate whereby a bed of agglomerated granules is formed, and thereafter cold air at a temperature not exceeding 75 F. is passed through a bed of the agglomerated granules.
  • the mixture of sodium tripolyphosphate and chlorinated trisodium phosphate may contain one or more other compatible alkaline-reacting water soluble salts, and preferably it contains from 5% to 40% particulate sodium silicate, consisting of one or more forms having an average weight ratio of SiO, to Na O of 1:1 to 3.6: 1. Particularly satisfactory results are obtained when the silicate has a ratio of about 2:1 or consists of a mixture having an average ratio of about 2: 1.
  • anhydrous sodium tripolyphosphate is of the so-called granular grade, that is having particle size such that not more than 20% passes a 100 mesh U.S. test sieve. Normally at least 15% of sodium tripolyphosphate by weight of the composition is used. If less is used it becomes increasingly diilicult to obtain satisfactory agglomerates though in some cases as little as 10% may 3,598,743 Patented Aug. 10, 1971 ice.
  • tripolyphosphate may be used to constitute the balance of the composition apart from the chlorinated trisodium phosphate and the aqueous silicate used in the process.
  • the preferred compositions contain about 25- 50% by weight of sodium tripolyphosphate (anhydrous).
  • chlorinated trisodium phosphate is used to designate a composition consisting of trisodium phosphate and sodium hypochlorite in intimate association in a crystalline form.
  • the proportion in the composition of the invention can vary quite widely according to the intended use of the product, for instance from 1% to about 75% by weight, but for most purposes a content of 5 to 50% by weight is preferable.
  • an organic surface active agent is also present in the composition.
  • This can be of any type compatible with the chlorinated phosphate, but usually a low foaming surface active agent, especially a nonionic detergent, is preferred.
  • Polypropylenoxypolyethylene oxide condensates such as the Pluronics (trade mark, Wyandotte Chemical Corporation) are very suitable.
  • the condensation products of ethylene oxide with long chain primary or secondary alcohols are usually employed at up to about 3% by weight, but a higher proportion of surface active agent may be used if it does not inake the product too sticky.
  • Foam suppressors may be used in the composition of this invention it control of foam is desired.
  • alkyl acid phosphates particularly as combined with mineral oil, as disclosed by Hathaway et al. in U.S. Patent 3,399,144, granted Aug. 27, 1968.
  • Minor amounts of other compatible components commonly included in detergent compositions may be added, such as colors, perfumes, stabilizers for the chlorinated phosphate,
  • the dry materials namely, sodium tripolyphosphate, solid sodium silicate if any, and chlorinated trisodium phosphate are mixed together in any suitable mixing device, such as its content of sodium tripolyphosphate; the type of mixing device; and the like.
  • the amount should be such as to cause the particulate mixture to form a bed of agglomerated granules, but not so great that its particulate nature is destroyed.
  • the solution to be sprayed on the dry mixture is usually at ambient temperature; i.e., between 50 and 100 F. If desired it may be warmed to as high as 160 F. for better atomization.
  • a liquid nonionic detergent When a liquid nonionic detergent is used it may be sprayed onto the mixture before, at the same time as, or after the silicate.
  • foam suppressors and minor liquid constituents such as perfume, color dispersion in water, etc., may be sprayed on in admixture with the nonionic detergent or separately.
  • the process may be carried out batchwise or continuously.
  • the solid components are metered at the appropriate rates into the mixing device and sprayed continuously with metered amounts of the liquids from one or more atomiurs.
  • the product consisting of agglomerated granules leaving the agglomerating stage of the process is usually warm as a result of the heat of hydration of the sodium tripolyphosphate, and usually feels moist.
  • a stream of cold air is then passed through the bed of agglomerated granules in any suitable vessel.
  • the air temperature must not exceed 75 F.; particularly good results have been obtained with air at 60-70 F.
  • This treatment may be car ried out batchwise or continuously, and it serves inter alia to cool the granules and to render them crisp and free-flowing; hence it is referred to as crisping air.
  • the shape of the vessel is not critical provided that care is taken that the air flow is substantially evenly distributed over the cross section of the bed of product.
  • the volumetric flow rate of air may be suflicient to fluidize the bed or it may be lower than this.
  • the duration of the treatment by air depends among other things upon the air temperature and rate of flow. Usually it is about /2 to 1 /2 hours when the air flow is sufficient to fluidize the bed of granules and about 1 to 3 hours if the flow is insufiicient to fluidize the bed.
  • a volumetric air flow rate that is at least one-fourth of that which would be just suflicient to fiuidize the granules. If the air treatment is to be carried out continuously the desired duration can be provided by appropriate choice of the amount of material in the bed in relation to the throughput, for instance such that the mean residence time is about one hour when the bed is fluidized.
  • the product is cooled, for example, from about 90 F. to about 70 F., and rendered crisp to the touch and free flowing. The drying which takes place is slight, is only incidental to the process, and is not in any way critical. As little as moisture loss is usual based on the weight of the composition, though up to 3% can be tolerated.
  • Example I 39.3 parts by weight of granular anhydrous sodium tripolyphosphate, of particle size such that not over 20% by weight passed a 100 mesh U.S. sieve, 18.4 parts of C soluble silicate (crystalline sodium silicate having weight ratio of SiO :Na O of 2.0:1 and containing 83% solids), and 20.3 parts of chlorinated trisodium phosphate were mixed together in an inclined pan granulator of 22 inches diameter. A solution consisting of parts C soluble" silicate and 10 parts water, at 120 F., was sprayed onto the dry mixture with continuous mixing in the rotating pan granulator by means of an air-atomized paint-spray gun. Thereafter, 2 parts of Pluronic L62 were sprayed on using similar spraying equipment.
  • C soluble silicate crystalline sodium silicate having weight ratio of SiO :Na O of 2.0:1 and containing 83% solids
  • chlorinated trisodium phosphate were mixed together in an inclined pan granulator of 22 inches diameter.
  • Pluronic L62 is the trade name of Wyandotte Chemical Corporation for a propylene oxide/ethylene oxide condensate of average molecular weight 22002800.
  • Air at 65 F. was passed up through this bed of agglomerated granules for 80 minutes at a velocity sufiicient to fluidize the product.
  • the resulting product was free flowing and had little tendency to cake in storage. Moisture loss was .6% by weight of the composition.
  • Example II Compositions having the constitution given below were made by a method analogous to that of Example I, except that the air was passed through the bed of agglomerates at about 30% of the rate needed to just fluidize the bed. All composition percentages in this table are on a weight basis.
  • Weight ratio SiOz/NmO 2.0 Amount of solution, percent 10 Concentration of solution solids, percent Crisping air temperature Crlsping time (hours)--. Moisture loss, percent Available chlorine, percent:
  • Example 111 Additional examples of granular detergent compositions that can be prepared by the process of Example I of the instant invention are given in the table below, the ingredients of which are defined as follows:
  • compositions when prepared by the process of Example I, have resistance to the loss of available chlorine in storage, have improved flow properties, and have resistance to caking in storage. Comparable results are obtained when the silicate solution for spray-on is at 70 F.
  • a process for preparing a granular detergent composition comprising the steps of:
  • a process for preparing a granular detergent composition comprising the steps of:
  • aqueous solution of sodium silicate contains from to by weight of the composition of silicate solids (total of SiO and Na O), and wherein the cold air is passed through the agglomerated granules for /2 to 1 /2 hours at a rate sufiicient to fiuidize the granules.
  • aqueous solution of sodium silicate contains from 30% to 50% by Weight of the composition of silicate solids (total of SiO and Na O), and wherein the cold air is passed through the agglomerated granules for l to 3 hours at a volumetric flow rate that is not suflicient to fluidize the granules but is at least one-fourth of that flow rate which would be just suflicient to fiuidize them.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

GRANULAR DISHWASHING DETERGENT COMPOSITIONS ARE PREPARED BY DRY-MIXING SODIUM TRIPOLYPHOSPHATE AND CHLORINATED TRISODIUM PHOSPHATE, SPRAYING AQUEOUS SODIUM SILICATE THEREON TO FORM AGGLOMERATED GANULES, AND COOLING BY PASSING COLD AIR AT A TEMPERATURE NOT EXCEEDING 75*F. THROUGH A BED OF THE GRANULES.

Description

U.S. Cl. 252-99 5 Claims ABSTRACT OF THE DISCLOSURE Granular dishwashing detergent compositions are prepared by dry-mixing sodium tripolyphosphate and chlorinated trisodium phosphate, spraying aqueous sodium silicate thereon to form agglomerated granules, and cooling by passing cold air at a temperature not exceeding 75 F. through a bed of the granules.
BACKGROUND OF THE INVENTION This invention relates to the processing of detergent agglomerates comprising sodium tripolyphosphate, chlorinated trisodium phosphate, and sodium silicate. Such agglomerates find wide application in dishwashing, especially in automatic dishwashing machines.
General disclosures relating to the composition and the agglomeration of automatic dishwashing products can be found in U. S. Patents 2,480,579 and 3,248,330. U.S. Patent 2,895,916, granted on July 21, 1959 to Milenkevich et al., mentions a cooling and aging step after agglomeration is completed to improve resistance to caking on storage. U .8. 3,247,118, granted on Apr. 19, 1966 to Matthaei, discloses a treatment of agglomerates with hot air to partially dry them.
Despite these contributions, the products made by priorart processes have continued to show a need for improvement in chlorine stability (that is, resistance to loss of available chlorine in storage), flow properties, and resistance to caking in storage.
SUMMARY OF THE INVENTION According to this invention there is provided a process for preparing a granular detergent composition wherein a particulate mixture of substantially anhydrous sodium tripolyphosphate and chlorinated trisodium phosphate is sprayed with an aqueous solution of sodium silicate whereby a bed of agglomerated granules is formed, and thereafter cold air at a temperature not exceeding 75 F. is passed through a bed of the agglomerated granules.
DETAILED DESCRIPTION The mixture of sodium tripolyphosphate and chlorinated trisodium phosphate may contain one or more other compatible alkaline-reacting water soluble salts, and preferably it contains from 5% to 40% particulate sodium silicate, consisting of one or more forms having an average weight ratio of SiO, to Na O of 1:1 to 3.6: 1. Particularly satisfactory results are obtained when the silicate has a ratio of about 2:1 or consists of a mixture having an average ratio of about 2: 1.
Preferably the anhydrous sodium tripolyphosphate is of the so-called granular grade, that is having particle size such that not more than 20% passes a 100 mesh U.S. test sieve. Normally at least 15% of sodium tripolyphosphate by weight of the composition is used. If less is used it becomes increasingly diilicult to obtain satisfactory agglomerates though in some cases as little as 10% may 3,598,743 Patented Aug. 10, 1971 ice.
give an acceptable product. At the other extreme, as much as 60% tripolyphosphate may be used to constitute the balance of the composition apart from the chlorinated trisodium phosphate and the aqueous silicate used in the process. The preferred compositions contain about 25- 50% by weight of sodium tripolyphosphate (anhydrous).
The term chlorinated trisodium phosphate is used to designate a composition consisting of trisodium phosphate and sodium hypochlorite in intimate association in a crystalline form. The proportion in the composition of the invention can vary quite widely according to the intended use of the product, for instance from 1% to about 75% by weight, but for most purposes a content of 5 to 50% by weight is preferable.
Preferably, a minor proportion of an organic surface active agent is also present in the composition. This can be of any type compatible with the chlorinated phosphate, but usually a low foaming surface active agent, especially a nonionic detergent, is preferred. Polypropylenoxypolyethylene oxide condensates, such as the Pluronics (trade mark, Wyandotte Chemical Corporation) are very suitable. Also useful are the condensation products of ethylene oxide with long chain primary or secondary alcohols. Usually such liquid or pasty nonionics are employed at up to about 3% by weight, but a higher proportion of surface active agent may be used if it does not inake the product too sticky.
Foam suppressors may be used in the composition of this invention it control of foam is desired. Especially suitable are the alkyl acid phosphates, particularly as combined with mineral oil, as disclosed by Hathaway et al. in U.S. Patent 3,399,144, granted Aug. 27, 1968. Minor amounts of other compatible components commonly included in detergent compositions may be added, such as colors, perfumes, stabilizers for the chlorinated phosphate,
and tarnish inhibitors.
In carrying out the agglomerating stage of the process the dry materials, namely, sodium tripolyphosphate, solid sodium silicate if any, and chlorinated trisodium phosphate are mixed together in any suitable mixing device, such as its content of sodium tripolyphosphate; the type of mixing device; and the like. The amount should be such as to cause the particulate mixture to form a bed of agglomerated granules, but not so great that its particulate nature is destroyed. Usually between about 10% and 40%,
by weight of the detergent composition, of a solution containing 20-60% (preferably 30-50%) of silicate solids (total of SiO; and Na O) gives satisfactory results. The solution to be sprayed on the dry mixture is usually at ambient temperature; i.e., between 50 and 100 F. If desired it may be warmed to as high as 160 F. for better atomization.
When a liquid nonionic detergent is used it may be sprayed onto the mixture before, at the same time as, or after the silicate. The above mentioned foam suppressors and minor liquid constituents, such as perfume, color dispersion in water, etc., may be sprayed on in admixture with the nonionic detergent or separately.
The process may be carried out batchwise or continuously. In the latter case the solid components are metered at the appropriate rates into the mixing device and sprayed continuously with metered amounts of the liquids from one or more atomiurs.
The product consisting of agglomerated granules leaving the agglomerating stage of the process is usually warm as a result of the heat of hydration of the sodium tripolyphosphate, and usually feels moist. A stream of cold air is then passed through the bed of agglomerated granules in any suitable vessel. The air temperature must not exceed 75 F.; particularly good results have been obtained with air at 60-70 F. This treatment may be car ried out batchwise or continuously, and it serves inter alia to cool the granules and to render them crisp and free-flowing; hence it is referred to as crisping air. The shape of the vessel is not critical provided that care is taken that the air flow is substantially evenly distributed over the cross section of the bed of product. Good results have been obtained using a vessel whose height was two to three times its diameter, the air entering through a sintered disc or a matrix of holes across the cross section of the vessel near the bottom. The volumetric flow rate of air may be suflicient to fluidize the bed or it may be lower than this. The duration of the treatment by air depends among other things upon the air temperature and rate of flow. Usually it is about /2 to 1 /2 hours when the air flow is sufficient to fluidize the bed of granules and about 1 to 3 hours if the flow is insufiicient to fluidize the bed. To avoid an excessively long crisping treatment it is preferred to use a volumetric air flow rate that is at least one-fourth of that which would be just suflicient to fiuidize the granules. If the air treatment is to be carried out continuously the desired duration can be provided by appropriate choice of the amount of material in the bed in relation to the throughput, for instance such that the mean residence time is about one hour when the bed is fluidized. In the course of the air treatment the product is cooled, for example, from about 90 F. to about 70 F., and rendered crisp to the touch and free flowing. The drying which takes place is slight, is only incidental to the process, and is not in any way critical. As little as moisture loss is usual based on the weight of the composition, though up to 3% can be tolerated.
Example I 39.3 parts by weight of granular anhydrous sodium tripolyphosphate, of particle size such that not over 20% by weight passed a 100 mesh U.S. sieve, 18.4 parts of C soluble silicate (crystalline sodium silicate having weight ratio of SiO :Na O of 2.0:1 and containing 83% solids), and 20.3 parts of chlorinated trisodium phosphate were mixed together in an inclined pan granulator of 22 inches diameter. A solution consisting of parts C soluble" silicate and 10 parts water, at 120 F., was sprayed onto the dry mixture with continuous mixing in the rotating pan granulator by means of an air-atomized paint-spray gun. Thereafter, 2 parts of Pluronic L62 were sprayed on using similar spraying equipment. (Pluronic L62 is the trade name of Wyandotte Chemical Corporation for a propylene oxide/ethylene oxide condensate of average molecular weight 22002800.) This formed a bed of agglomerated granules, a portion of which was transferred to a 4 ins. diameter vertical tube to form a bed of agglomerated granules about 12 ins. deep. Air at 65 F. was passed up through this bed of agglomerated granules for 80 minutes at a velocity sufiicient to fluidize the product. The resulting product was free flowing and had little tendency to cake in storage. Moisture loss was .6% by weight of the composition.
By way of comparison, 44.5 parts of the same granular sodium triployphosphate, 31 parts of a 50:50 mixture (by weight) of sodium metasilicate (ratio SiO :Na O of 1:1, 57% solids) and Silicate M (Crystalline Sodium Silicate having weight ratio SiO :Na 0 of 3.3:1, 83% solids) and 20.0 parts of chlorinated trisodium phosphate were mixed together in the same pan granulator. A mixture of 3 parts Pluronic L62 and 1 part of water was sprayed onto the mixture with continuous mixing in the rotating pan granulator. Cold air was not passed through the bed of 4 agglomerated granules that formed, and the resulting product had poor flow properties and caked on storage.
The two products were stored in polyethylene bags at F. and tested after the intervals stated below for available chlorine content. The results were as follows:
Product of Comparative invention, product, percent percent available Cl available Cl Time (weeks):
Example II Compositions having the constitution given below were made by a method analogous to that of Example I, except that the air was passed through the bed of agglomerates at about 30% of the rate needed to just fluidize the bed. All composition percentages in this table are on a weight basis.
Sodium tripolyphosphate, percent.. Chlorinated trisodium phosphate,
percent 50 id 0 soluble" sodium silicate percent Pluronic L62, percent. Water, percent Spray on silicate solution:
Weight ratio: SiOz/NmO 2.0 Amount of solution, percent 10 Concentration of solution solids, percent Crisping air temperature Crlsping time (hours)--. Moisture loss, percent Available chlorine, percent:
As made Stored 100 F 2 weeks.. 4 weeks as a:
All the products with the exception of F (which was included for comparison) were free flowing powders, and all had, as shown, better chlorine stability then P.
Example 111 Additional examples of granular detergent compositions that can be prepared by the process of Example I of the instant invention are given in the table below, the ingredients of which are defined as follows:
Weight Percent ratio silicate SiOgHNa O solids All entries in the following table are weight percent based on the total composition.
Tergitol 15-S3.. TE
These compositions, when prepared by the process of Example I, have resistance to the loss of available chlorine in storage, have improved flow properties, and have resistance to caking in storage. Comparable results are obtained when the silicate solution for spray-on is at 70 F.
What is claimed is:
1. A process for preparing a granular detergent composition comprising the steps of:
(a) mixing together from 15% to 60% by weight of the composition of substantially anhydrous sodium tripolyphosphate with from 1% to 75% by weight of the composition of chlorinated trisodium phosphate; to form a particulate mixture,
(b) with continuous mixing, spraying onto said particulate mixture from 10% to 40% by weight of the composition of an aqueous solution of sodium silicate having a weight ratio of SiO to N21 O of from 1:1 to 3.6:]; to form agglomerated granules, and
(c) passing cold air at a temperature not exceeding 75 F. through said agglomerated agglomerated granules in an amount sufiicient to render the granules crisp and free flowing.
2. A process for preparing a granular detergent composition comprising the steps of:
(a) mixing together (i) from 25% to 50% by weight of the composition of substatnially anhydrous sodium tripolyphosphate having a particle size such that not more than 20% passes a 100 mesh U.S. test sieve, (ii) from 5% to 50% by weight of the composition of chlorinated trisodium phosphate, and (iii) from 5% to 40% by weight of the composition of particulate sodium silicate consisting of one or more forms having an average weight ratio of SiO /Na O of 1:1 to 3.611, to form a particulate mixture,
(b) with continuous mixing, spraying onto said particulate mixture from to 40% by weight of the composition of an aqueous solution of sodium silicate containing from to 60% by weight of the solution of silicate solids (total of SiO and Na 0) having a weight ratio of SiO to Na O of from 1:1 to 3.6:]; to form agglomerated granules, and
(c) passing cold air at 60-70 F. through said agglomerated granules in an amount sufficient to render the granules crisp and free flowing.
3. The process of claim 2 wherein the aqueous solution of sodium silicate contains from to by weight of the composition of silicate solids (total of SiO and Na O), and wherein the cold air is passed through the agglomerated granules for /2 to 1 /2 hours at a rate sufiicient to fiuidize the granules.
4. The process of claim 2 wherein the aqueous solution of sodium silicate contains from 30% to 50% by Weight of the composition of silicate solids (total of SiO and Na O), and wherein the cold air is passed through the agglomerated granules for l to 3 hours at a volumetric flow rate that is not suflicient to fluidize the granules but is at least one-fourth of that flow rate which would be just suflicient to fiuidize them.
5. The process of claim 2 wherein the mixing is carried out by means of an inclined pan granulator.
References Cited UNITED STATES PATENTS 2,895,916 7/1959 Milenkevich et a1. 252-99 3,247,118 4/1966 Matthaei 25299 3,359,207 12/1967 Kaneko et a1. 25299 3,520,815 7/1970 Wessells 252-99 MAYER WEINBLATT, Primary Examiner U.S. Cl. X.R. 23313
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Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3888781A (en) * 1972-09-05 1975-06-10 Procter & Gamble Process for preparing a granular automatic dishwashing detergent composition
US3933670A (en) * 1973-11-12 1976-01-20 Economic Laboratories, Inc. Process for making agglomerated detergents
US4077897A (en) * 1976-02-13 1978-03-07 The Procter & Gamble Company Process for preparing detergent compositions
US4169806A (en) * 1978-08-09 1979-10-02 The Procter & Gamble Company Agglomeration process for making granular detergents
US4182683A (en) * 1976-05-17 1980-01-08 Berk Gunter H Process for the manufacture of a dishwashing detergent
US4191661A (en) * 1977-11-07 1980-03-04 The Procter & Gamble Company Alkaline dishwasher detergent
US4199467A (en) * 1978-05-04 1980-04-22 The Procter & Gamble Company Alkaline dishwasher detergent
US4199468A (en) * 1977-11-07 1980-04-22 The Procter & Gamble Company Alkaline dishwasher detergent
US4207197A (en) * 1978-08-09 1980-06-10 The Procter & Gamble Company Agglomeration process for making granular detergents
US4228025A (en) * 1979-06-29 1980-10-14 The Procter & Gamble Company Agglomeration process for making granular detergents
US4329246A (en) * 1977-11-07 1982-05-11 The Procter & Gamble Company Alkaline dishwasher detergent
US4464281A (en) * 1983-07-28 1984-08-07 Lever Brothers Company Stabilized bleach-sensitive dyes in automatic dishwasher detergent compositions
FR2616156A1 (en) * 1987-06-05 1988-12-09 Colgate Palmolive Co DETERGENT POWDER COMPOSITION COMPRISING A SILICATE FOR AUTOMATIC DISHWASHING, METHOD FOR MANUFACTURING SAME, AND METHOD FOR USING THE SAME
US5213705A (en) * 1985-04-30 1993-05-25 Ecolab Inc. Encapsulated halogen bleaches and methods of preparation and use

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3888781A (en) * 1972-09-05 1975-06-10 Procter & Gamble Process for preparing a granular automatic dishwashing detergent composition
US3933670A (en) * 1973-11-12 1976-01-20 Economic Laboratories, Inc. Process for making agglomerated detergents
US4077897A (en) * 1976-02-13 1978-03-07 The Procter & Gamble Company Process for preparing detergent compositions
US4182683A (en) * 1976-05-17 1980-01-08 Berk Gunter H Process for the manufacture of a dishwashing detergent
US4329246A (en) * 1977-11-07 1982-05-11 The Procter & Gamble Company Alkaline dishwasher detergent
US4191661A (en) * 1977-11-07 1980-03-04 The Procter & Gamble Company Alkaline dishwasher detergent
US4199468A (en) * 1977-11-07 1980-04-22 The Procter & Gamble Company Alkaline dishwasher detergent
US4199467A (en) * 1978-05-04 1980-04-22 The Procter & Gamble Company Alkaline dishwasher detergent
US4169806A (en) * 1978-08-09 1979-10-02 The Procter & Gamble Company Agglomeration process for making granular detergents
US4207197A (en) * 1978-08-09 1980-06-10 The Procter & Gamble Company Agglomeration process for making granular detergents
US4228025A (en) * 1979-06-29 1980-10-14 The Procter & Gamble Company Agglomeration process for making granular detergents
US4464281A (en) * 1983-07-28 1984-08-07 Lever Brothers Company Stabilized bleach-sensitive dyes in automatic dishwasher detergent compositions
US5213705A (en) * 1985-04-30 1993-05-25 Ecolab Inc. Encapsulated halogen bleaches and methods of preparation and use
FR2616156A1 (en) * 1987-06-05 1988-12-09 Colgate Palmolive Co DETERGENT POWDER COMPOSITION COMPRISING A SILICATE FOR AUTOMATIC DISHWASHING, METHOD FOR MANUFACTURING SAME, AND METHOD FOR USING THE SAME
BE1003812A5 (en) * 1987-06-05 1992-06-23 Colgate Palmolive Co Detergent composition having silicate powder for automatic washing dishes, manufacturing process and method of use.

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