US3741913A - Process for preparing spray dried detergent compositions - Google Patents

Process for preparing spray dried detergent compositions Download PDF

Info

Publication number
US3741913A
US3741913A US00117073A US3741913DA US3741913A US 3741913 A US3741913 A US 3741913A US 00117073 A US00117073 A US 00117073A US 3741913D A US3741913D A US 3741913DA US 3741913 A US3741913 A US 3741913A
Authority
US
United States
Prior art keywords
ethylene oxide
slurry
alkyl
ingredients
detergent composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US00117073A
Inventor
A Waag
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DOMSJO AB
DOMSJO SW AB
Original Assignee
DOMSJO AB
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from SE6608678A external-priority patent/SE313630C/en
Priority claimed from SE294469A external-priority patent/SE319259B/xx
Application filed by DOMSJO AB filed Critical DOMSJO AB
Application granted granted Critical
Publication of US3741913A publication Critical patent/US3741913A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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 ; Methods for using cleaning compositions
    • C11D11/02Preparation in the form of powder by spray drying
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/34Derivatives of acids of phosphorus
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/34Derivatives of acids of phosphorus
    • C11D1/345Phosphates or phosphites
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • 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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0026Low foaming or foam regulating compositions
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/905Agent composition per se for colloid system making or stabilizing, e.g. foaming, emulsifying, dispersing, or gelling
    • Y10S516/907The agent contains organic compound containing phosphorus, e.g. lecithin
    • Y10S516/908The compound contains repeating -OCnH2n-, i.e. repeating unsubstituted oxyalkylene

Abstract

A PROCESS IS PROVIDED FOR PREPARING SPRAY DRIED SUBSTANTIALLY HOMOGENEOUS DETERGENT COMPOSITIONS FROM AQUEOUS SLURRIES CONTAINING SURFACE-ACTIVE ETHYLENE OXIDE ADDUCTS WHEREIN PRIOR TO SPRAY DRYING THE AQUEOUS SLURRY, AN ORGANIC MONO- OR POLYPHOSPHATE ESTER IS INCORPORATED WITH THE SURFACE-ACTIVE ETHYLLENE OXIDE ADDUCT AND OTHER INGREDIENTS EMPLOYED IN THE DETERGENT COMPOSITION, IN ORDER TO INHIBIT THE SLURRY FROM SEPARATING INTO DIFFERENT LAYERS SO THAT THE PARTICULATE DETERGENT COMPOSITION PRODUCTED WILL BE SUBSTANTIZLLY HOMOGENEOUS AND LOW FOAMING AND HAVE GOOD CLEANING POWER. THE PHOSPHATE ESTER MAY BE ADDED TO THE INGREDIENTS OF THE DETERGENT COMPOSITION PRIOR TO, DURING OR SUBSEQUENT TO THE PREPARATION OF THE AQUEOUS SLURRY TO THE INGREDIENTS. DETERGENT COMPOSITIONS ARE ALSO PROVIDED, WHICH CAN BE PREPARED EMPLOYING THE ABOVE PROCESS, CONSISTING ESSENTIALLY OF AT LEAST ONE SURFACE-ACTIVE ETHYLENE OXIDE ADDUCT, AND AN ORGANIC MONO- OR POLYPHOSPHATE ESTER, AND OPTIONALLY, INORGANIC BUILDERS, OPTICAL WHITENERS, CHELATING AGENTS AND DIRT CARRIERS, SUCH AS CARBOXYMETHYL CELLULOSE.

Description

United States Patent Oflice 3,741,913 Patented June 26, 1973 3,741,913 PROCESS FOR PREPARING SPRAY DRIED DETERGENT COMPOSITIONS Ake Waag, Stenungsund, Sweden, assignor to M och Domsjo Aktiebolag, Ornskoldsvik, Sweden No Drawing. Continuation of abandoned application Ser. No. 648,248, June 23, 1967. This application Feb. 19, 1971, Ser. No. 117,073 Claims priority, application Sweden, June 23, 1966, 8,678/ 66 Int. Cl. Clld 3/36 U.S. Cl. 252-544 14 Claims ABSTRACT OF THE DISCLOSURE A process is provided for preparing spray dried substantially homogeneous detergent compositions from aqueous slurries containing surface-active ethylene oxide adducts wherein prior to spray drying the aqueous slurry, an organic monoor polyphosphate ester is incorporated with the surface-active ethylene oxide adduct and other ingredients employed in the detergent composition, in order to inhibit the slurry from separating into different layers so that the particulate detergent composition produced will be substantially homogeneous and low foaming and have good cleaning power. The phosphate ester may be added to the ingredients of the detergent composition prior to, during or subsequent to the preparation of the aqueous slurry of the ingredients.
Detergent compositions are also provided, which can be prepared employing the above process, consisting essentially of at least one surface-active ethylene oxide adduct, and an organic monoor polyphosphate ester, and optionally, inorganic builders, optical whiteners, chelating agents and dirt carriers, such as carboxymethyl cellulose.
This application is a continuation of copending application Ser. No. 648,248, filed June 23, 1967 and now abandoned.
The present invention is concerned with a method for preparing spray dried detergent compositions from aqueous slurries containing surface active ethylene oxide adducts and organic and inorganic builders.
Detergent compositions suitable for use in modern washing machines and for synthetic fabrics require surface active substances possessing particularly good qualities with regard to low foaming ability, strong cleaning ability and a small afiinity for the fabric. Surfactants which possess such properties are ethylene oxide adducts of different chemical substances, such as alkyl phenols, fatty alcohols, fatty acids, fatty acid alkanol amides and alkyl mercaptans and ethylene oxide-propylene oxide block polymers. In addition to the just mentioned ethylene oxide adducts large quantities of builders comprised of organic and/ or inorganic substances are included in such detergents. The inorganic substances are primarily comprised of water-soluble alkaline builder salts, such as phosphates for instance alkali metal tripolyphosphates, alkali metal silicates, alkali metal borates, alkali metal carbonates, alkali metal hydrocarbonates, alkali metal sulphates, alkali metal chlorides etc., and inorganic peroxides (bleaching agents), whereas the organic substances comprise optical whiteners, dirt carriers such as carboxymethyl cellulose, and chelating agents, such as ethylene diamine tetraacetic acid etc. When preparing the detergent composition the ingredients are first mixed with water and, because of the high substance concentration (40-60 percent by weight), a slurry is obtained, which is then dried in heat to powder form. The drying method adopted is the spray drying method; the slurry being ejected under high pressure through a nozzle in the top of a tower and allowed to flow downwards whilst coming into contact with hot air, whereby small granules of detergent composition are formed. It is important that these granules have the same composition throughout, so that a detergent possessing good and reproducible properties is obtained. However, when preparing detergent compositions containing ethylene oxide adducts difficult problems present themselves during the spray drying process, in that the slurry to be dried is not sufficiently stable and often separates into different layers; whereby the homogeneity of the dried composition is jeopardized and there is also a risk that the nozzles will become blocked. Before the slurry can be sprayed it is necessary that it remains stable for at least one minute upon completion of the agitating process. Attempts have been made to alleviate these problems, which are not so much concerned with the solubility in water of the ingredients forming a part of the slurry as with their ability of together forming stable slurries or aqueous dispersions by strong agitation or by the addition of different substances; but hitherto these methods have given rise to appreciable disadvantages in the form of incomplete and deficient dispersion, increased foam formation, decrease in the cleansing ability of the composition, and high cost.
The present invention is intended to eliminate or substantially reduce the above mentioned deficiencies encountered in the preparation of spray dried detergent compositions of aqueous slurries containing surface active ethylene oxide adducts and conventional builders. It has been found that the said disadvantages are, according to the invention, surprisingly eliminated if, prior to, during or subsequent to preparing the aqueous slurry, one or more known phosphate esters, possibly condensed as condensate with two, three or four groups of the general formula or alkali salts or ammonium salts thereof are added to the slurry, in which formula R and R are alike or different and represent hydrogen or a group where R represents a saturated or unsaturated, straight or branched alkyl or alkenyl radical having a total of 4-22, preferably 8-18, carbon atoms in the alkyl or alkenyl portion or a mono, di or trialkyl substituted phenol having a total of 6-24, preferably 8-18 carbon atoms in the alkyl portion, wherewith R and R do not at the same time comprise hydrogen, and n is -30, preferably 5-25; after which the obtained slurry is spray dried in a manner known per se. The addition of such phosphate esters has been found to impart a very good stability to the slurry, in addition there occurs no depreciation in the cleansing ability of the detergent composition, nor does it give rise to heavy foam formation. The compounds can be produced at a relatively low price and have Such a strong efifect that only small amounts need be added, and the requirement of additional additives in the form of other substances such as hydrotropes and solubilizers is unnecessary.
The phosphate esters which may be used according to the invention may be prepared by phosphating in a known manner compounds including a residue having the gen eral formula wherein R and ll have the above disclosed significance. Such compounds are suitably ethylene oxide adducts of mono, di or trialkyl substituted phenols with a total of 6-24, preferably 25-18, carbon atoms in the alkyl portion and preferably 6-30 moles ethylene oxide such as nonylphenol having 8-1-6 moles ethylene oxide, dinonylphenol having 8-16 moles ethylene oxide, tri-sec.-butylphenol having 10-30 moles ethylene oxide, octylphenol having 8-16 moles ethylene oxide, octylcresol having 8- moles ethylene oxide.
Other suitable compounds are ethoxylated, saturated or unsaturated primary aliphatic alcohols having preferably 8-18 carbon atoms and preferably 3-20 moles eth-.
ylene oxide, for instance coconut fatty alcohol having 6-10 moles ethylene oxide, oleyl alcohol having 10-20 moles ethylene oxide, tridecylalcohol having 10-20 moles ethylene oxide, cetylstearyl alcohol having 10-30 moles ethylene oxide etc.
Additional compounds which are suitable for producing the phosphate esters are such where n in the above formula is 0, Le. nonethoxylated compounds containing the residue R defined according to the above, such as mono, di or trialkyl substituted phenols, and saturated or unsaturated primary aliphatic alcohols. Examples of such compounds are nonyl phenol, dinonyl phenol, trisec.-butyl phenol, 2-ethyl hexanol, dodecylalcohol, cetyl alcohol, stearylalcohol, oleyl alcohol, tridecyl alcohol etc.
As starting material for the phosphating process, mixtures of the above mentioned compounds may also used, e.g. mixtures of ethoxylated compounds and also mixtures of ethoxylated and nonethoxylated products. With regard to such mixtures it is particularly suitable to phosphatize mixtures of ethoxylaed alkyl phenols having a total of 6-24, preferably 8-18 carbon atoms in the alkyl portion and primary, aliphatic, straight or branched alcohols having 4-8 carbon atoms; the mole ratio of ethoxylated alkylphenol/aliphatic alcohol being from 1:1 to 1:9.
An example of such a mixture is a mixture containing nonyl phenol having 6 moles ethylene oxide and 2-ethylhexanol, in the mole ratio of about 1:1. Another example is a mixture of oleyl alcohol having 14 moles ethylene oxide and tridecyl alcohol having 8 moles ethylene oxide in the mole ratio of 1:1.
An example of phosphating agents used in preparing the phosphate esters are polyphosphoric acid (partially hydrated P 0 retailed by Stauffer Chemical Co.), P 0 and H PO Mixtures of other phosphating agents may also be used. In the esterifying reaction, the phosphating agent is reacted at an elevated temperature, preferably 50-100 C., with the compound or compounds to be phosphated, preferably for a period of time of from 0.5- 4 hours, after which the formed acid product is preferably neutralized with alkali hydroxide or NH whereby the neutralizing process may be effected before, or dur ing the preparation of the slurry to be spray dried. The mole ratio of phosphating agent/phosphating mixture is 4 of great importance and varies according to the composition of the phosphating mixture and the phosphating agent used. It is generally suitable to cause 1-5 moles of phosphating agent to react with 1-5 moles of the organic compound. When using polyphosphoric acid (73-85 percent by weight P 0 as the phosphating agent or phosphating ethoxylated alkyl phenols and/or primary aliphatic alcohols it is particularly expedient that the amount of polyphosphoric acid comprises 1-l.5 moles per mole ethoxylated alkyl phenol. When using phosphoric acid as the phosphating agent it is particularly advantageous with regard to the phosphating of mixtures of ethoxylated alkyl phenols and primary aliphatic alcohols if the mole ratio of P O /phosphating mixture is from 1:3 to 1.5:3 and the mole ratio ethoxylated alkyl phenol/ primary aliphatic alcohol lies between 1:1 and 1:9. It is also of particular advantage in this connection if the mole ratio P O /ethoxylated alkylphenol is less than 1:2. A mixture of phosphating esters having the above disclosed formula is generally obtained during the phosphating reaction, whereby monoesters, diesters or triesters are obtained, according to the prevailing reaction conditions, the constituents taking part in the reaction and the amount of phosphating agent. When phosphating with a polyphosphoric acid of an alcohol or an ethylene oxide adduct a mixture of mono and diesters is usually obtained; monoesters forming the predominate percentage of the mixture. When conducting such a phosphating process smaller amounts of polyphosphoric esters are also obtained e.g. in the form of pyrophosphoric acid diesters, polyphosphoric acid triesters, triphosphoric acid diesters etc., which may, of course also be used according to the present invention. When phosphating a mixture of ethylene oxide adducts and aliphatic alcohols with orthophosphoric acid a mixture is obtained, which contains primarily diesters. It is impossible to obtain exact information concerning the compostion of the phosphating mixtures due to the fact that as yet, no suitable analysis method for this purpose has been suggested. During such phosphating reactions insignificant amounts of triesters are also formed; which naturally may also be included in the phosphate ester mixture added according to the invention.
Suitable surface active ethylene oxide adducts which can be used in the detergent compositions according to the present invention are ethylene oxide adducts of alkyl phenols, fatty acids, fatty alcohols, fatty acid alcohol amides, alkyl mercaptans and ethylene oxide/propylene oxide block polymers. An example of such adducts are mono, di and trialkylphenols having l-50 moles ethylene oxide and a total of 8-22 carbon atoms in the alkyl portion, primary, aliphatic alcohols having 1-100 moles ethylene oxide and a saturated or unsaturated, straight or branched alkyl or alkenyl portion having a total of 8-22 carbon atoms, alkyl mercaptans having 1-50 moles ethylene oxide, fatty acid mono or di-alkanol amides having 1-10 moles ethylene oxide and saturated or unsaturated, straight or branched alkyl or alkenyl portion with a total of 8-22 carbon atoms and the alkanol portion deriving from ethanol, propanol or butanol groups, ethylene oxide/propylene oxide block polymers, where the polypropylene oxide portion or portions comprise the hydrophobic portion and polyethylene oxide the hydrophilic portion. According to the present invention mixtures of the above mentioned products are also suitable. Naturally the effect of the phosphate ester additive according to the present invention is also present when the surface active ethylene oxide adduct is used together with other types of surfactants, e.g. together with soap, alkyl aryl sulphonates, alkyl sulphates, alkyl sulphonates, alkyl isothionates, alkyl taurides, alkyl phenol ether sulphonates, alkyl phenol ether sulphates, alkyl ether sulphates, alkyl naphthalene sulphonates, sulphonates of naphthalene formaldehyde condensates, carboxymethylated alkyl or alkyl phenol ethylene oxide adducts etc.
The above disclosed water-soluble alkaline builders included in the detergent composition generally comprise 30-60% of the weight of the slurry. Typical formulations of the ingredients in the slurry are given below:
Percent by weight Surface active agent 5-20 Dirt carrier, e.g. carboxymethyl cellulose 0.5-2.5
Bleaching agent, e.g. alkali metal perborate 5-20 Builder I, e.g. sodium silicate 38-40 B 5-20 Builder II, e.g. sodium sulphate 5-20 Builder III, e.g. sodium tripolyphosphate 10-50 Water 30-60 Suitable amounts of phosphate esters required for achieving the effect according to the invention are from 1 to 50% calculated on the amount of surface active agent included in the composition, preferably 5-25% by weight being used. The addition of the phosphate esters may be effected at any time during the slurrying process, i.e. during any of the steps taken in mixing the various ingredients; but it is also possible to add the phosphate esters to any of the ingredients, e.g. the surface active agent, before preparing the slurry, likewise as it is also possible to add the phosphate esters in question to the prepared slurry. The phosphate esters are preferably added during the preparation of the slurry, which gives the advantage that the included surface active ethylene oxide adduct does not salt out at any time during the procedure.
Although, as a rule, additions of very small amounts of phosphate esters give a satisfactory result (as can be seen from the following examples) it is, if desired, possible to add to the slurry other substances such as benzene sulphonate, alkyl benzene sulphonates, toluene sulphonate, xylene sulphonate, alkyl naphthalene sulphonates, carbamide, dicyanamide, amino oxides, propylene glycol, hexylene glycol, which increase the solubility of the ethylene oxide adduct in solvents, for instance water. It should also be mentioned, however, that the nature of the effect of such substances is different from the elfect of the phosphate esters added according to the present invention, which have a special and surprising effect in aqueous slurries containing surface active ethylene adducts and high concentrations of electrolytes.
The invention is illustrated in the following examples.
EXAMPLE 1 In a containing 100 parts by weight water the following ingredients were slurried unter agitation, in the given order:
Parts by weight (1) Dinonyl phenol, 16 moles ethylene oxide 15 (2) Sodium carboxymethyl cellulose 1 (3) Water glass 38-40 B. 15 (4) Sodium sulphate 29 (5) Sodium tripolyphosphate 40 The slurry was then heated to 80 C., the ethylene oxide adduct salted out after 10 seconds. When 10% by weight of the ethylene oxide adduct (1.5 parts by weight) was exchanged against the sodium salt of an esterification product of 1.3 moles polyphosph'oric acid (calculated as P and 1 mole nonylphenol having 8 moles ethylene oxide but otherwise under the same conditions no salting out could be observed during an observation period of 30 mins., and the slurry proved to be completely stable and intact. When sprayed dried it gave a homogeneous powder.
EXAMPLE 2 Example 1 was repeated but with an addition of 10% by weight calculated on the amount of ethylene oxide adduct (1.5 parts by weight) of the potassium salt of a phosphate ester obtained by reacting 1.3 moles polyphosphoric acid (calculated as P 0 with 1 mole nonylphenol having 12 moles ethylene oxide. No separation was observed during an observation period of 30 mins. upon the addition of the phosphate ester according to the invention. The slurry according to the invention gave a homogeneous powder upon subsequent spray drying.
EXAMPLE 3 Example 1 was repeated but with an addition of 10% by weight calculated on the amount of ethylene oxide adduct of potassium salt of a phosphate ester obtained by reacting 1.3 moles polyphosphoric acid (calculated as P 0 and 1 mole nonylphenol having 16 moles ethylene oxide. When adding the phosphate ester according to the invention no separation could be noticed during an observation period of 30 mins. The slurry gave a homogeneous powder when subjected to spray drying process.
EXAMPLE 4 A slurry was prepared containing 19 parts by weight of water and the following ingredients added in the order given below:
Parts by weight (1) Nonyl phenol with 10 moles ethylene oxide 10 (2) Sodium carboxymethyl cellulose 1.5 (3) Water glass 38 B. 30.5 (4) Sodium sulphate 35.0
When heating to C. a separation was observed after only 10 secs. When 30% by weight (3 parts by weight) of the ethylene oxide adduct was exchanged against a phosphate ester obtained by reacting 0.34 mole orthophosphoric acid and 1.5 moles P 0 on one side and a mixture of 1.1 moles nonyl phenol having 6 moles ethylene oxide and 1.9 moles Z-ethyl hexanol on the other side, which was neutralized with NaOH to pH 8.5 (in one percent aqueous solution), no separation was observed during an observation period of 30 mins. The slurry prepared according to the invention gave a homogeneous product when subjected to a spray drying operation.
EXAMPLE 5 A slurry was prepared containing 110 parts by weight of water and the following ingredients. The phosphate ester was added in a first stage, whereupon the ingredients were added in the order given below:
(5) Sodium tripolyphosphate Parts by weight (1) Phosphate ester according to Example 2 3.6 (2) Coconut fatty alcohol having 7 moles ethylene oxide 14.4 (3) Sodium carboxymethyl cellulose 1.0 (4) Water glass 38 B. 5.0 (5) Sodium sulphate 40.0 (6) Sodium tripolyphosphate 31.0 (7) Sodium perborate 5.0
The obtained slurry was stable during the complete preparation period and when heated to 80 C. no signs of separation were noticed after an observation period of 30 mins. The slurry gave a homogeneous powder when sub- -jected to a spray drying operation.
EXAMPLE 6 EXAMPLE 7 A slurry was prepared of parts by weight of water and the following ingredients added in the order in which they appear.
Parts by weight (1) Oleyl alcohol with 14 moles ethyl oxide 6 .5- (2) Tridecyl alcohol having 8 moles ethylene oxide 6.5 (3) Sodium carboxymethyl cellulose 1.0 (4) Water glass 40 B. 15.0 (5) Sodium carbonate 30.0 (6) Sodium tripolyphosphate 39.0
Subsequent to slurrying the said ingredients 2.0 parts by Weight of the sodium salt of a phosphate ester obtained by reacting 1.5 moles polyphosphoric acid (calculated as P and 2.3 moles 2-ethyl hexanol was added. When heated to 80 C. no signs of separation were observed during an observation period of 30 mins. and the said slurry gave a homogeneous powder when subjected to a spray drying operation.
Having regard to the foregoing disclosures, the following is claimed as the inventive and patentable embodiments thereof:
1. A process for preparing a substantially homogeneous spray dried detergent composition from an aqueous slurry containing about 30% to about 60% by weight of water and having solid ingredients consisting essentially of about 5% to about 20% by weight of a surface-active ethylene oxide adduct of an alkyl phenol, fatty alcohol, fatty acid alkanol amide, alkyl mercaptan or an ethylene oxidepropylene oxide block polymer, and about 30% to about 60% by weight of water-soluble inorganic alkaline builder salts, said slurry having a tendency to separate into phases, which process comprises incorporating in said slurry prior to spray drying an amount to inhibit phase separation within the range from about 1 to about 50% by weight based on the surface-active ethylene oxide adduct of an organic phosphate ester having the general formula:
wherein R and R can be the same or different and are selected from the group consisting of hydrogen and R(OCH CH wherein R is selected from the group consisting of alkyl and alkenyl radicals containing from about four to about twenty-two carbon atoms, and a mono-, dior trialkyl-substituted phenyl, the allyl containing from about six to about twenty-four carbon atoms, at least one of R and R being R(OCH CH and n is an integer from 0 to about 30; and spray-drying the aqueous slurry to form particles of uniform composition.
2. A process in accordance with claim 1 which comprises incorporating the organic phosphate ester in the detergent composition while adding water to the ingredients to form a slurry thereof.
3. A process in accordance with claim 1 which comprises adding the organic phosphate ester to the aqueous slurry of the detergent composition.
4. A process in accordance with claim 1 which comprises incorporating the organic phosphate ester with the detergent composition prior to adding water to the ingredients to form a slurry thereof.
5. A process in accordance with claim 1, wherein the organic phosphate ester is selected from the group consisting of alkali metal salts and ammonium salts of such phosphate esters.
6. A substantially homogeneous spray dried detergent composition consisting essentially of about 5 to about 20 parts by Weight of at least one surface-active ethylene oxide adduct of an alkyl phenol, fatty-alcohol, fatty acid, fatty acid alkanol amide, or alkyl mercaptan or an ethylene oxide-propylene oxide block polymer; about 30 to about 60 parts by weight of water soluble inorganic alkaline builder salts; and from about 1 to about 50% by weight based on the surface-active ethylene oxide adduct of an organic phosphate ester having the general formula:
Ri-O r O l) [RrO O-H] wherein R and R can be the same or different and are selected from the group consisting of hydrogen and R(OCH CH wherein R is selected from the group consisting of alkyl and alkenyl radicals containing from about four to about twenty-two carbon atoms, and a mono-, dior trialkyl-substituted phenyl, the alkyl containing from about six to about twenty-four carbon atoms, at least one of R and R being R(0C'H CH and n is an integer from 0 to about 30.-
7. A substantially homogeneous spray dried detergent composition in accordance with claim 6 wherein the organic phosphate ester is selected from the group consisting of alkali metal salts and ammonium salts of such organic phosphate esters.
8. A substantially homogeneous spray dried detergent composition in accordance with claim 6 wherein at least one of R and R is a mono-, dior trialkyl-substituted phenyl having from about eight to about eighteen carbon atoms in the alkyl portion.
9. A substantially homogeneous spray dried detergent compositon in accordance with claim 6 wherein at least one of R and R is alkyl having from about eight to about eighteen carbon atoms.
10. A substantially homogeneous spray dried detergent composition in accordance with claim 6 wherein at least one of R and R is derived from mixtures of ethoxylated alkyl phenols containing from about six to about twentyfour carbon atoms in the alkyl portion and primary, aliphatic, straight or branched alcohols containing from about four to about eight carbon atoms.
11. A substantially homogeneous spray dried detergent composition in accordance with claim 10 in which the ethoxylated alkyl phenol and the aliphatic alcohol are present in a mol ratio of about 1:1 to about 1:9.
12. A slurry adapted upon spray drying to yield homogeneous detergent particles, consisting essentially of about 5% to about 20% of a surface-active ethylene oxide adduct of an alkyl phenol, fatty alcohol, fatty acid alkanol amide, alkyl mercaptan or an ethylene oxide-propylene oxide block polymer; and from about 30% to about 60% by weight of water-soluble inorganic alkaline builder salts; slurried in from about 30% to about 60% by weight of water; said slurry having a tendency to separate into phases; and an amount sufficient to inhibit phase separation within the range of from about 1% to about 50% by weight based on the surface-active ethylene oxide adduct of an organic phosphate ester having the general wherein R and R can be the same or different and are selected from the group consisting of hydrogen and R(OCH CH wherein R is selected from the group consisting of alkyl and alkenyl radicals containing from aboutfour to about twenty-two carbon atoms, and a mono-, dior trialkyl-substituted phenyl, the alkyl containing from about six to about twenty-four carbon atoms, at least one of R and R being R(OCH CH and n is an integer from 0 to about 30.
13. A slurry in accordance with claim 12 and also containing from about 0.5% to about 2.5% by'weight of sodium carboxymethyl cellulose.
14. A slurry in accordance with claim 12 and also containing from about to about 20% by weight of a bleaching agent.
References Cited UNITED STATES PATENTS 5 11/1967 Behrens 252-137 12/1966 Dupre et a1. 252-135 1/1968 Cooper et al. 252-99 9/1964 Schlitz et a1. 252-137 9/ 19 68 Quimby 252-89 X 8/1964 Inamorato 252-138 6/1967 Inamorato 252-135 X 6/ 1965 Metcalf et a1. 252-135 2/1964 Grifo et a1. 252-135 10 OTHER REFERENCES General Aniline & Film Corp., Tech. Bulletin 7543- 094; GAFAC Surfactants, :610, PE 510, 1.0529, 1960.
Mayhew et al.: Phosphate Surfactants-Properties and Uses, Soap and Chemical Specialties, April 1962, pp. -58, 95, 93; May 1962, pp. -81, 167, 169.
HERBERT B. GUYNN, Primary Examiner H. A. PITLICK, Assistant Examiner US. Cl. X.R. 252-89, 525
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Dated lacent No. 3, 741,913 I l'uveucofle) A .Waag
' June 26, 1973 It is certified that error appears in theabove-identified patent: and that said Letters Patent ere hereby corrected as shown below:
' Column 3; line 4'7 ,Column 5, line 49 Column 3, line 51 Column 4, line 3'7 Column 5, line 48 1 Column 5, line 67 Column 7, line 48,
Claim 1 -"In a containing" should "be -;--In container containing-- 'also used" -;should be -al'so' be used-- "ethoxylaed should be --et hoxylated-- "compost ion" should be --composit ion-- "unter" sliould be --un'der- "sprayed" should be --sprayf:- f
"'allylf" should be -la1k '1-5Q Signed and sealed this 2nd day, of' ril 1m.
(SEAL) Attest:
EDWARD M .FLETCHER, JR Attesting Officer C MARSHALL DANN C'ommi s si oner of Pate nt s
US00117073A 1966-06-23 1971-02-19 Process for preparing spray dried detergent compositions Expired - Lifetime US3741913A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
SE6608678A SE313630C (en) 1966-06-23 1966-06-23 PROCEDURE FOR PREPARING SPAIN DRYED DETERGENT COMPOSITIONS
US64824867A 1967-06-23 1967-06-23
SE294469A SE319259B (en) 1969-03-04 1969-03-04
US210161A US3869412A (en) 1966-06-23 1971-12-20 Surface-active compositions having controlled foaming properties and process for controlling foam therewith

Publications (1)

Publication Number Publication Date
US3741913A true US3741913A (en) 1973-06-26

Family

ID=27484477

Family Applications (2)

Application Number Title Priority Date Filing Date
US00117073A Expired - Lifetime US3741913A (en) 1966-06-23 1971-02-19 Process for preparing spray dried detergent compositions
US210161A Expired - Lifetime US3869412A (en) 1966-06-23 1971-12-20 Surface-active compositions having controlled foaming properties and process for controlling foam therewith

Family Applications After (1)

Application Number Title Priority Date Filing Date
US210161A Expired - Lifetime US3869412A (en) 1966-06-23 1971-12-20 Surface-active compositions having controlled foaming properties and process for controlling foam therewith

Country Status (9)

Country Link
US (2) US3741913A (en)
AT (1) AT270029B (en)
CA (1) CA928183A (en)
DE (2) DE1617160B2 (en)
DK (2) DK131351B (en)
FI (2) FI46735C (en)
GB (2) GB1159643A (en)
NL (2) NL6708745A (en)
NO (1) NO121968C (en)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4048085A (en) * 1975-04-18 1977-09-13 Lever Bros. Co. Preparation of detergent compositions
US4126586A (en) * 1976-02-10 1978-11-21 Lever Brothers Company Process of spray drying nonionic surfactant-containing detergents also containing a cationic nitrogen compound
US4140650A (en) * 1976-11-26 1979-02-20 Lever Brothers Company Process for manufacture of detergent powders
US4155882A (en) * 1973-08-01 1979-05-22 Lever Brothers Company Process for preparing particulate detergent compositions containing nonionic surfactants
US4198308A (en) * 1973-07-23 1980-04-15 Colgate Palmolive Company Manufacture of free-flowing fabric softening detergent
US4239641A (en) * 1978-08-03 1980-12-16 Basf Aktiengesellschaft Use of polyhydric alcohols, carboxylic acids, hydroxy-carboxylic acids and/or their esters with polyhydric alcohols as viscosity regulators
US4313847A (en) * 1978-06-15 1982-02-02 Ici Americas Inc. Surfactant compositions
US4652391A (en) * 1984-09-22 1987-03-24 Henkel Kommanditgesellschaft Auf Aktien High powder density free-flowing detergent
US4661281A (en) * 1984-07-02 1987-04-28 Henkel Kommanditgesellschaft Auf Aktien Process for the production of a spray-dried nonionic washing aid
US4675128A (en) * 1984-12-31 1987-06-23 Henkel Kommanditgesellschaft Auf Aktien Alkane sulfonates as viscosity regulators
US5192461A (en) * 1991-08-23 1993-03-09 Enthone-Omi, Inc. Aqueous degreasing solution having high free alkalinity
US5372741A (en) * 1991-11-27 1994-12-13 Ethone-Omi, Inc. Aqueous degreasing composition and process
US5446188A (en) * 1991-03-21 1995-08-29 Henkel Kommanditgesellschaft Auf Aktien Process for the production of highly concentrated fatty alcohol sulfate pastes
US6060444A (en) * 1993-12-30 2000-05-09 Ecolab Inc. Method of making non-caustic solid cleaning compositions
US6164296A (en) * 1993-12-30 2000-12-26 Ecolab Inc. Method of removing waxy/fatty soils from ware with a combination of a nonionic silicone surfactant and a nonionic surfactant
US6369021B1 (en) 1999-05-07 2002-04-09 Ecolab Inc. Detergent composition and method for removing soil
US6673765B1 (en) * 1995-05-15 2004-01-06 Ecolab Inc. Method of making non-caustic solid cleaning compositions
WO2004067194A2 (en) * 2003-01-31 2004-08-12 Reckitt Benckiser N.V. Aqueous cleaning compositions
US20050256226A1 (en) * 2002-02-28 2005-11-17 Dean Thetford Phosphate esters dispersants
US20080139704A1 (en) * 2006-12-06 2008-06-12 Boral Material Technologies Inc. Method and composition for controlling the viscosity of latex compositions that include fly ash

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2193871B1 (en) * 1972-07-25 1977-07-22 Colgate Palmolive Co
FR2193868B1 (en) * 1972-07-25 1977-04-01 Colgate Palmolive Co
US4049558A (en) * 1972-07-25 1977-09-20 Colgate-Palmolive Co. Free flowing phosphate ester compositions for post addition to detergents
GB1492938A (en) * 1974-01-11 1977-11-23 Procter & Gamble Ltd Low sudsing detergent compositions
GB1506392A (en) * 1974-05-09 1978-04-05 Unilever Ltd Detergent powder production
IE42854B1 (en) * 1975-06-13 1980-11-05 Ciba Geigy Ag Process for removing foam from aqueous systems
DE2532802C2 (en) * 1975-07-23 1983-03-10 Hoechst Ag, 6000 Frankfurt Wool detergent
FR2283219A2 (en) * 1975-08-26 1976-03-26 Unilever Nv DETERGENT POWDER PRODUCTION
GB1571502A (en) * 1976-01-23 1980-07-16 Unilever Ltd Detergent compositions
GB1571501A (en) * 1976-01-23 1980-07-16 Unilever Ltd Detergent compositions
US4070298A (en) * 1976-07-26 1978-01-24 Olin Corporation Defoaming detergent additive
FI783563A (en) * 1977-12-01 1979-06-02 Sandoz Ag FOERBAETTRINGAR I OCH ANGAOENDE ORGANISKA FOERENINGAR
CH637304A5 (en) * 1978-11-03 1983-07-29 Ciba Geigy Ag FOAM ABSORBENT FOR AQUEOUS SYSTEMS.
US4298494A (en) * 1979-03-27 1981-11-03 Lever Brothers Company Shampoo
JPS5631077A (en) * 1979-08-21 1981-03-28 Teijin Ltd Treating composition of raw yarn for high speed elongating abrasion false twisting process and raw yarn adhered with said composition and method
US4492646A (en) * 1980-02-05 1985-01-08 The Procter & Gamble Company Liquid dishwashing detergent containing anionic surfactant, suds stabilizer and highly ethoxylated nonionic drainage promotor
NZ199235A (en) * 1980-12-17 1985-02-28 Unilever Plc Controlled-sudsing detergent compositions
DE3240403A1 (en) * 1982-11-02 1984-05-03 Henkel KGaA, 4000 Düsseldorf USE OF LOW MOLECULAR ORGANIC COMPOUNDS AS A VISCOSITY REGULATOR FOR HIGH VISCOSE TECHNICAL TENSIDE CONCENTRATES
US4505836A (en) * 1982-07-28 1985-03-19 Tp Industrial, Inc. Plastic bottle cleaner composition and method
JPS60224606A (en) * 1984-04-23 1985-11-09 Kao Corp Effect enhancer for insecticide
FR2564853B1 (en) * 1984-05-28 1987-08-21 Lesieur Cotelle LIQUID COMPOSITION FOR CLEANING HARD SURFACES.
US4749516A (en) * 1985-09-24 1988-06-07 S. C. Johnson & Son, Inc. Anionic emulsion pre-spotting composition
DE3627023A1 (en) * 1986-08-09 1988-02-11 Hoechst Ag PIGMENT DISPERSIONS, METHOD FOR THEIR PRODUCTION AND THEIR USE
GB8628613D0 (en) * 1986-11-29 1987-01-07 Horsell Graphic Ind Ltd Developing fluid for lithographic plates
GB8713574D0 (en) * 1987-06-10 1987-07-15 Albright & Wilson Liquid detergent compositions
MY103673A (en) * 1988-01-14 1993-08-28 Kao Corp Detergent composition
US5110487A (en) * 1989-04-03 1992-05-05 Chevron Corporation Enhanced oil recovery method using surfactant compositions for improved oil mobility
US5273682A (en) * 1989-09-22 1993-12-28 Chevron Research And Technology Company Viscosity control additives for foaming mixtures
US5034158A (en) * 1989-10-24 1991-07-23 Shell Oil Company Monionic surfactant based powdered laundry detergent formulation containing an alkenyl or alkyl carboxysulfonate component
US5035838A (en) * 1989-10-24 1991-07-30 Shell Oil Company Nonionic surfactant based liquid detergent formulation containing an alkenyl or alkyl carboxysulfonate component
GB2238530A (en) * 1989-10-31 1991-06-05 Grace W R & Co Antifoaming and defoaming compositions
US5037474A (en) * 1989-11-27 1991-08-06 Morton International, Inc. Bitumen antistripping agent
DE4032909A1 (en) * 1990-10-17 1992-04-23 Henkel Kgaa METHOD FOR PRODUCING ALKYL SULFATE PASTES WITH IMPROVED FLOWABILITY
CA2081932A1 (en) * 1991-11-07 1993-05-08 Zia Haq Cosmetic composition
GB9218792D0 (en) * 1992-09-04 1992-10-21 Unilever Plc Skin cleansing composition
EP0728475A3 (en) * 1995-02-21 1997-03-19 Kao Corp Skin cleanser
US5827808A (en) * 1997-01-31 1998-10-27 The Procter & Gamble Company Dishwashing method
DE19928923A1 (en) * 1999-06-24 2000-12-28 Cognis Deutschland Gmbh Foam-controlled solid laundry detergent containing surfactants and antifoam, useful in domestic laundry, contains (poly)ethylene glycol monoethers with mixture of long-chain alk(en)yl groups as nonionic surfactants
DE19928924A1 (en) * 1999-06-24 2000-12-28 Cognis Deutschland Gmbh Foam-controlled solid laundry detergent containing surfactants and antifoam, useful in domestic laundry, contains (poly)ethylene glycol monoether with mixture of long-chain alk(en)yl groups as nonionic surfactant
DE602005011618D1 (en) * 2004-07-15 2009-01-22 Akzo Nobel Nv PHOSPHATED ALKANOL, ITS USE AS HYDROTROP AND CLEANING COMPOSITION WITH THE COMPOUND
US20060252666A1 (en) * 2005-05-09 2006-11-09 Dennis Sheirs Household cleaning composition
WO2007146956A2 (en) 2006-06-12 2007-12-21 Rhodia Inc. Hydrophilized substrate and method for hydrophilizing a hydrophobic surface of a substrate
EP2152839B1 (en) * 2007-06-12 2018-11-14 Solvay USA Inc. Detergent composition with hydrophilizing soil-release agent and methods for using same
EP2152845B1 (en) * 2007-06-12 2017-03-29 Solvay USA Inc. Hard surface cleaning composition with hydrophilizing agent and method for cleaning hard surfaces
JP5613559B2 (en) * 2007-06-12 2014-10-22 ローディア インコーポレイティド Mono-, di- and polyol alkoxylate phosphate esters and methods of use thereof in oral care formulations
AU2008266168B2 (en) * 2007-06-12 2014-07-10 Rhodia Inc. Mono-di-and polyol phosphate esters in personal care formulations
WO2009014821A2 (en) * 2007-07-20 2009-01-29 Rhodia Inc. Method for recovering crude oil from a subterranean formation
EP3175844A1 (en) 2010-04-09 2017-06-07 Pacira Pharmaceuticals, Inc. Large diameter synthetic membrane vesicles
CN103492542B (en) * 2011-04-13 2016-05-25 Elc管理公司 Be applicable to the mild anion surfactant of personal care composition
WO2014072840A1 (en) 2012-11-12 2014-05-15 Galaxy Surfactants Ltd. Flowable, high active, aqueous fatty alkyl sulfates
US10626350B2 (en) 2015-12-08 2020-04-21 Ecolab Usa Inc. Pressed manual dish detergent

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE596967A (en) * 1959-11-12
BE632444A (en) * 1962-05-18
US3235627A (en) * 1962-05-18 1966-02-15 Rohm & Haas Alkali soluble and alkali stable compositions comprised predominantly of phosphate monoesters
US3523902A (en) * 1965-04-07 1970-08-11 Wyandotte Chemicals Corp Controlled suds detergent
US3400148A (en) * 1965-09-23 1968-09-03 Procter & Gamble Phosphonate compounds
US3341467A (en) * 1967-03-03 1967-09-12 Grace W R & Co Method of inhibiting foaming in aqueous systems

Cited By (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4198308A (en) * 1973-07-23 1980-04-15 Colgate Palmolive Company Manufacture of free-flowing fabric softening detergent
US4155882A (en) * 1973-08-01 1979-05-22 Lever Brothers Company Process for preparing particulate detergent compositions containing nonionic surfactants
US4048085A (en) * 1975-04-18 1977-09-13 Lever Bros. Co. Preparation of detergent compositions
US4126586A (en) * 1976-02-10 1978-11-21 Lever Brothers Company Process of spray drying nonionic surfactant-containing detergents also containing a cationic nitrogen compound
US4140650A (en) * 1976-11-26 1979-02-20 Lever Brothers Company Process for manufacture of detergent powders
US4313847A (en) * 1978-06-15 1982-02-02 Ici Americas Inc. Surfactant compositions
US4239641A (en) * 1978-08-03 1980-12-16 Basf Aktiengesellschaft Use of polyhydric alcohols, carboxylic acids, hydroxy-carboxylic acids and/or their esters with polyhydric alcohols as viscosity regulators
US4661281A (en) * 1984-07-02 1987-04-28 Henkel Kommanditgesellschaft Auf Aktien Process for the production of a spray-dried nonionic washing aid
US4652391A (en) * 1984-09-22 1987-03-24 Henkel Kommanditgesellschaft Auf Aktien High powder density free-flowing detergent
US4675128A (en) * 1984-12-31 1987-06-23 Henkel Kommanditgesellschaft Auf Aktien Alkane sulfonates as viscosity regulators
US5446188A (en) * 1991-03-21 1995-08-29 Henkel Kommanditgesellschaft Auf Aktien Process for the production of highly concentrated fatty alcohol sulfate pastes
US5192461A (en) * 1991-08-23 1993-03-09 Enthone-Omi, Inc. Aqueous degreasing solution having high free alkalinity
US5372741A (en) * 1991-11-27 1994-12-13 Ethone-Omi, Inc. Aqueous degreasing composition and process
US6489278B1 (en) 1993-12-30 2002-12-03 Ecolab Inc. Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent
US20040254090A1 (en) * 1993-12-30 2004-12-16 Ecolab Inc. Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent
US7199095B2 (en) 1993-12-30 2007-04-03 Ecolab Inc. Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent
US6060444A (en) * 1993-12-30 2000-05-09 Ecolab Inc. Method of making non-caustic solid cleaning compositions
US20060040841A1 (en) * 1993-12-30 2006-02-23 Ecolab Inc. Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent
US6956019B2 (en) 1993-12-30 2005-10-18 Ecolab Inc. Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent
US6664219B1 (en) 1993-12-30 2003-12-16 Ecolab Inc. Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent
US6164296A (en) * 1993-12-30 2000-12-26 Ecolab Inc. Method of removing waxy/fatty soils from ware with a combination of a nonionic silicone surfactant and a nonionic surfactant
US6767884B2 (en) 1993-12-30 2004-07-27 Ecolab Inc. Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent
US6673765B1 (en) * 1995-05-15 2004-01-06 Ecolab Inc. Method of making non-caustic solid cleaning compositions
US20040077516A1 (en) * 1999-05-07 2004-04-22 Ecolab Inc. Detergent composition and method for removing soil
US6812202B2 (en) 1999-05-07 2004-11-02 Ecolab Inc. Detergent composition and method for removing soil
US6649586B2 (en) 1999-05-07 2003-11-18 Ecolab Inc. Detergent composition and method for removing soil
US6525015B2 (en) 1999-05-07 2003-02-25 Ecolab Inc. Detergent composition and method for removing soil
US6369021B1 (en) 1999-05-07 2002-04-09 Ecolab Inc. Detergent composition and method for removing soil
US20050256226A1 (en) * 2002-02-28 2005-11-17 Dean Thetford Phosphate esters dispersants
WO2004067194A2 (en) * 2003-01-31 2004-08-12 Reckitt Benckiser N.V. Aqueous cleaning compositions
WO2004067194A3 (en) * 2003-01-31 2004-11-18 Reckitt Benckiser Nv Aqueous cleaning compositions
US20080139704A1 (en) * 2006-12-06 2008-06-12 Boral Material Technologies Inc. Method and composition for controlling the viscosity of latex compositions that include fly ash
US7879926B2 (en) * 2006-12-06 2011-02-01 Boral Material Technologies Inc. Method and composition for controlling the viscosity of latex compositions that include fly ash

Also Published As

Publication number Publication date
DE2008777A1 (en) 1970-11-05
DK131351B (en) 1975-06-30
NO121968B (en) 1971-05-03
GB1300829A (en) 1972-12-20
NL6708745A (en) 1967-12-27
US3869412A (en) 1975-03-04
NL7003103A (en) 1970-09-08
CA928183A (en) 1973-06-12
DK131351C (en) 1975-11-24
GB1159643A (en) 1969-07-30
DE1617160A1 (en) 1972-04-20
AT270029B (en) 1969-04-10
FI46735C (en) 1981-01-05
FI54325B (en) 1978-07-31
DK140046B (en) 1979-06-11
DK140046C (en) 1979-11-12
FI46735B (en) 1973-02-28
DE1617160B2 (en) 1975-04-24
NO121968C (en) 1977-06-13
FI54325C (en) 1978-11-10

Similar Documents

Publication Publication Date Title
US3741913A (en) Process for preparing spray dried detergent compositions
US3331896A (en) Method of preparing alkali soluble phosphate esters of hydroxylic organic compounds
US3850831A (en) Liquid detergent compositions containing surfactants and peroxide bleaching agents
EP0238638B1 (en) Process for preparing particulate detergent compositions
GB918430A (en) Phosphate esters of surface active agents
DE2412839C3 (en)
US3168478A (en) Highly alkaline surface active compositions
US3294693A (en) Phosphorylated surfactants as hydrotropes
US4438014A (en) Nonionic surfactants for automatic dishwasher detergents
US3970595A (en) Heavy duty alkaline liquid surfactant concentrate
GB717407A (en) Formed detergents
US4364777A (en) Prevention of foam in alkaline cleansing bath by the use of mixed formals of polyglycol ethers
DE1929193B2 (en) Softening detergent
US3816351A (en) Industrial car wash composition
US3775315A (en) Manufacture of ammonium polyphosphate
US3472784A (en) Detergent process
CA1083910A (en) Manufacture of detergent compositions
US3394083A (en) Effervescent builder compositions and detergent compositions containing the same
US3770855A (en) Process for producing phosphate ester surface active compositions
US4436642A (en) Nonionic surfactants for automatic dishwasher detergents
DE2547389A1 (en) Phosphate-free detergent - contg. nonionic surfactant having different degrees of ethoxylation and sodium aluminium silicate builder
DK148039B (en) wool detergent
US3150161A (en) Process for preparating organo-sulfates
US3810847A (en) Process for preparing free-flowing alpha-olefin sulfonate powders while hydrolyzing sultones
US3562168A (en) Alkaline earth and amine salts of phosphate ester surfactants in dry cleaning compositions