US3850833A - Scouring cleanser composition - Google Patents

Scouring cleanser composition Download PDF

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Publication number
US3850833A
US3850833A US00341211A US34121173A US3850833A US 3850833 A US3850833 A US 3850833A US 00341211 A US00341211 A US 00341211A US 34121173 A US34121173 A US 34121173A US 3850833 A US3850833 A US 3850833A
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US
United States
Prior art keywords
sodium
group
bromide
solid particle
propylene glycol
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
US00341211A
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English (en)
Inventor
M Koceich
W Chirash
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.)
Colgate Palmolive Co
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Colgate Palmolive Co
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Filing date
Publication date
Priority to GB302672A priority Critical patent/GB1378923A/en
Priority to AU38225/72A priority patent/AU473970B2/en
Priority to FR7202191A priority patent/FR2123356B1/fr
Priority to CA133,071A priority patent/CA943428A/en
Priority to DE2203141A priority patent/DE2203141C3/de
Priority to AT57172A priority patent/AT319442B/de
Priority to NLAANVRAGE7201035,A priority patent/NL172674C/xx
Priority to CH109872A priority patent/CH569083A5/xx
Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co
Priority to US00341211A priority patent/US3850833A/en
Application granted granted Critical
Publication of US3850833A publication Critical patent/US3850833A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40—Dyes ; Pigments
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B63/00—Lakes
    • 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
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395—Bleaching agents
    • C11D3/3951—Bleaching agents combined with specific additives
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395—Bleaching agents
    • C11D3/3955—Organic bleaching agents

Definitions

  • the present invention relates in general to cleansing compositions and in particular to the provision of small colored particles which may be incorporated into cleansing compositions, such colored particles having esthetic as well as functional value.
  • the greatest esthetic appeal seems to result from a composition that is colored with a combination of white and a blue or green color. That is, the particular cleasning product should contain some particles that are blue or green colored, and some particles, preferably the majority, that are white.
  • vari-colored cleansing compositions may be formulated by a method that is simple and inexpensive.
  • Another object is to provide a process for producing such colored particles in a simple and inexpensive manner.
  • the present invention therefor offers the following advantages.
  • the product exhibits equal or better performance to existing products, and in addition has the benefit of esthetic appeal.
  • the process of manufacture is simple and inexpensive, and existing plant equipment can be used. Further, the process can be used to produce colored solid particles for a variety of products.
  • a functional colored particle containing as essential ingredients (1 a bleach activator, (2) a pigment extender and binder, (3) a pigment and (4) a rapidly water soluble inert particulate carrier material.
  • the bleach activator is preferably an inorganic bromide compound, such as an alkali metal bromide that is substantially neutral and that is soluble in water.
  • an alkali metal bromide that is substantially neutral and that is soluble in water.
  • preferred compounds for use herein are sodium bromide, lithium bromide and potassium bromide.
  • a single component of the composition may serve as pigment extender and binder.
  • Such material may be, for example, propylene glycol, polyethylene glycol 300, propylene glycol phenol ether, or other suitable material. This material must be compatible with the pigment and other components of the colored particle, and must also be soluble in or miscible with water.
  • the pigments contemplated for use herein although encompassing a relatively broad class of materials, must nonetheless meet certain requirements.
  • the pigments best suited for use display substantial water dispersibility. Pigments classes as non-water dispersible form precipitates when added to aqueous media and accordingly would be unsuitable for use herein.
  • a further requirement with regard to pigment selection relates to color composition; thus, suitable pigments should have a reflectance in the 450 to 535 millimicron wave length region of the visible spectrum. This region corresponds to the blue through green colors.
  • the pigment material must be stable in the presence of hypohalide-liberating agents.
  • the pigment may be selected from animal pigments, mineral pigments, synthetic or artificial pigments, so long as the pigment material is not in any way detrimental to the function of the composition into which it is to be incorporated.
  • the phthalo cyanine pigments such as chromophthal green, are particularly suitable for use.
  • the carrier material or diluent for use in the invention is a rapidly water soluble, particulate material which is substantially neutral and inert with respect to the other materials used in the cleansing composition.
  • Such material may be for example, sodium chloride, potassium chloride or sodium sulfate.
  • the pigment, bleach activator and binder are essentially coated onto the outside of the particles of the carrier material.
  • the colored solid particles prepared according to the invention thus have a particle size of about 0.15 mm to 2.0 mm.
  • the preferred diameter size is about l.5 mm.
  • the method of preparation of the colored particles, according to the invention is as follows.
  • the carrier or diluent material and the bleach activator are dry blended; the pigment is added and dry mixed with the carrier and bleach activator mixture. Following this, the binder and pigment extender is added to the mixture and blended. The entire mixture must be blended for a period of time sufficient to assure uniform coating of the particles or conglomerates.
  • the colored particles as formulated herein are added to a cleansing composition, such as a scouring cleanser.
  • a scouring cleanser as provided by the present invention contains as essential ingredients (I) an abrasive material, (2) a hypohalide liberating agent, which acts as a bleach, and (3) a water soluble detergent.
  • the abrasive material may be chosen from a fairly wide range of materials, provided certain criteria are met.
  • the abrasive material should be substantially white colored, and should have a high light reflectance value, such as about 80-85 percent measured at 550 u.
  • the abrasive material should have a particle size of about .00l mm to 0.4 mm, and should be free of any acid, since this will have deleterious effects on any perfume that may optionally be included in the cleaner.
  • the abrasive material is employed in proportions of up to 95 and preferably 45 to 95 percent ofthe cleanser composition.
  • the hypohalide liberating bleaching agent to be included in the cleanser formulation is one which is capable of liberating hypochlorite chlorine and/or hypobromite bromine upon contact with aqueous media.
  • Such bleaching agents are, for example, heterocyclic N- bromo and N-chloro imides such as trichlorocyanuric acid, tribromocyanuric acid, dibromo and dichlorocyanuric acid, and salts thereof with water solubilizing cations such as potassium and sodium.
  • Suitable bleaching agents are N-brominated and N-chlorinated succinimid melonimid phthalimide and naphthalimide, the hydantoins, such as 1,3- dibromo and l,3-dichloro-5, S-dimethylhydantoin; N- monochloro-C, C-dimethylhydantoin methylene-bis (N-bromo-C, C-dimethyl-hydantoin); l,3-dibromo and l,3-dichloro5-isobutyhydantoin; l,3-bromo and 1,3- dichloro 5'methyl-5-ethylhydantoin; l,3'dibromo and l,3-dichloro 5,5-diisobutylhydantoin; l,3-dibromo and l,3-dichloro-S-methyI-S-n-
  • hypohalite-liberating agents comprise tribromomelamine and trichloromelamine. Dry, particulate, water soluble anhydrous inorganic salts are likewise suitable for use such as lithium hypochlorite and hypobromite.
  • the hypohalite-liberating agent may,
  • the present invention contemplates as an additional embodiment the use of bleaching agents capable of liberating hypochlorite as well as hypobromite such as, for example, the N-brominated, N'-chlorinated heterocyclic imides, as for example the N-bromo, N'chlorocyanuric acids and salts thereof, e.g., N- monobromo-N, N-dichlorocyanuric acid, N- monobromo-N-monochlorocyanuric acid, N- monobromo-N-monochlorocyanuric acid, sodium-N- monobromo-monochlorocyanurate, potassium-N- monobromo-N-monochlorocyanurate; and the N- brominated, N-chlorinated hydantoins, e.g., N-bromo- N-chloro-S, S-dimethylhydantoin and N-bromo-N- chloro-S-ethyl-S-methyl
  • hypohalide-liberating compound is employed in an amount of from 0.1 to 25 percent by weight of the composition, and preferably in an amount of from about 0.3 to 20 percent by weight thereof.
  • the detergent component of the compositions described herein compriseswater soluble organic detergent materials which are stable in the presence of the contemplated hypohalite-liberating compound.
  • organic detergents may be ofthe anionic, cationic, amphoteric or non-ionic types provided of course that they are compatible with the compositions as a whole and in the proportions employed.
  • the detergent may be provided in particulate solid form after ab sorption upon diatomaceous earth or other similar agents according to procedures well known in the art.
  • suitable anionic surface active agents include those surface active or detergent compounds which contain an organic hydrophobic group and an anionic solubilizing group.
  • anionic solubilizing groups are sulfonate, sulfate, carboxylate, phosphonate and phosphate.
  • anionic detergents which may be used in the compositions of the invention are the soaps, such as the sodium soaps of tallow, grease, coconut oil, tall oil and mixtures thereof; and the sulfated and sulfonated synthetic detergents, particularly those having about 8 to 26, and preferably about 12 to 22, carbon atoms to the molecule.
  • suitable synthetic anionic detergents there may be cited the higher alkyl mononuclear aromatic sulfonates such as the higher alkyl benzene sulfonates containing from 10 to 16 carbon atoms in the alkyl group in a straight or branched chain, e.g., the sodium salts of decyl, undecyl, dodecyl, (lauryl), tridecyl, tetradecyl, pentadecyl, or hexdecyl benzene sulfonate and the higher alkyl toluene, xylene and phenol sulfonates; alkyl naphthalene sulfonate, ammonium diamyl naphthalene sulfonate, and sodium dinonyl naphthalene sulfonate.
  • the higher alkyl mononuclear aromatic sulfonates such as the higher alkyl benzene
  • anionic detergents are the olefin sulfonates, including long chain alkeno sulfonates, long chain hydroxy-alkane sulfonates or mixtures of alkenesulfonates and hydroxy-alkane sulfonates.
  • sulfates of higher alcohols are sodium lauryl sulfate and sodium tallow alcohol sulfate. Turkey Red Oil or other sulfated oils, or sulfates of mono or digly-cerides of fatty acids (e.g.
  • alkyl poly (ethenoxy) ether sulfates such as the sulfates of the condensation products of ethylene oxide and lauryl alcohol (usually having 1 to 5 ethenoxy groups per molecule); lauryl or other higher alkyl glyceryl ether sulfonates; aromatic poly (ethenoxy) ether sulfates such as the sulfates of the condensation products of ethylene oxide and nonyl phenol (usually having l to oxyethylene groups per molecule preferably 2-l2) may be used.
  • the suitable anionic detergents include also the acyl sarcosinates (e.g. sodium lauroylsarcosinate) the acyl esters (e.g. oleic acid ester( of isothionates. and the acyl N-methyl taurides (e.g. potassium N-methyl lauroyl-or oleyl tauride).
  • acyl sarcosinates e.g. sodium lauroylsarcosinate
  • the acyl esters e.g. oleic acid ester( of isothionates.
  • the acyl N-methyl taurides e.g. potassium N-methyl lauroyl-or oleyl tauride
  • the most highly preferred water soluble anionic detergent compounds are the ammonium and substituted ammonium (such as mono. di and triethanolamine),
  • alkali metal such as calcium and magnesium
  • the particular salt will be suitably selected depending upon the particular formulation and the proportions therein.
  • Nonionic surface active agents include those surface active or detergent compounds which contain an organic hydrophobic group and a hydrophilic group which is a reaction product of a solubilizing group such as carboxylate, hydroxyl, amido or amino with ethylene oxide or with the polyhydration product thereof. polyethylene glycol.
  • nonionic surface active agents which may be used are the condensation products of alkyl phenols with ethylene oxide. e.g., the reaction product of isooctyl phenol with about 6 to 30 ethylene oxide units; condensation products of higher fatty alcohols such as tridecyl alcohol with ethylene oxide; ethylene oxide addends or monoesters of hexahydric alcohols and inner ethcrs thereof such as sorbitan monolaurate, sorbitol monooleatc and mannitan monopalmitate, and the condensation products of polypropylene glycol with ethylene oxide.
  • condensation products of alkyl phenols with ethylene oxide e.g., the reaction product of isooctyl phenol with about 6 to 30 ethylene oxide units
  • condensation products of higher fatty alcohols such as tridecyl alcohol with ethylene oxide
  • ethylene oxide addends or monoesters of hexahydric alcohols and inner ethcrs thereof such as sorbitan monol
  • Cationic surface active agents may also be employed.
  • Such agents are those surface active detergent compounds which contain an organic hydrophobic group and a cationic solubilizing group, such as the diamines such as those of the type RNl-lC H NH wherein R is an alkyl group of about 12 to 22 carbon atoms such as N- 2-aminoethyl stearyl amine and N-Z-amino-ethyl myristyl amine; amido-linked amines such as those of the type R'CONHC H NH wherein R is an alkyl group of about 9 to 20 carbon atoms.
  • N-Z-amino ethylstearyl amide and N-amino ethyl myristyl amide such as N-Z-amino ethylstearyl amide and N-amino ethyl myristyl amide; quaternary ammonium compounds such as ethyl-dimethylstearyl ammonium chloride, benzyl-dimethyl-stearyl ammonium chloride, benzyl-dimethyl-stearyl ammonium chloride. trimethyl stearyl ammonium chloride, trimethylcetyl ammonium bromide, dimethyl ethyl dilauryl ammonium chloride, dimethyl-propyl-myristyl ammonium chloride. and the corresponding methosulfates and acetates.
  • amphoteric detergents which may be used are N-alkyl-beta-aminopropionic acid; N-alkyl-beta-iminodipropionic acid, and N-alkyl, N,N- dimethyl glycine.
  • fatty imidazolines such as those made by reacting a long chain fatty acid (e.g. of 10 to 20 carbon atoms) with diethylene triamine and monohalocarboxylic acids having 2 to 6 carbon atoms, e.g. l-coco-5-hydroxyethyl-5-carboxymethylimidazoline; betaines containing a sulfonic group instead of the carboxylic group; betaines in which the long chain substituent is joined to the carboxylic group without an intervening nitrogen atom, e.g. inner salts of Z-trimethylamino fatty acids such as 2-trimethylaminolauric acid, and compounds of any of the previously mentioned types but in which the nitrogen atom is replaced by phosphorous are further examples.
  • fatty imidazolines such as those made by reacting a long chain fatty acid (e.g. of 10 to 20 carbon atoms) with diethylene triamine and monohalocarboxylic acids having 2 to 6 carbon atoms, e.g.
  • the detergent material is employed in concentrations ranging from about 0.5 to 30 parts by weight of the total composition with a range of l to 7 parts being particularly preferred.
  • the detergent may be added to the composition by spraying.
  • suitable detergent for use in the invention is Detax" which is a mixture of alkyl aryl sulfonates prepared by the Colgate-Palmolive Com-
  • the cleanser compositions may contain various other materials as well, such as builder salts and perfumes.
  • Some of the builder salts that may be included are trisodium phosphate, sodium acid pyrophosphate, sodium carbonate, tetrasodium pyrophosphate, sodium tripholyphosphate.
  • the builder salt is employed in amounts ranging up to about percent, i.e.. 0-95 percent by weight with a range of from about 3 to about 30 percent by weight of the composition being preferred.
  • a scouring cleanser was prepared of the following composition (percentages are by weight):
  • Example II To this composition, 2.7 percent by weight based on the total cleanser composition, of the colored particles prepared as in Example I were added.
  • the resulting cleansing compound which has a white powder containing small green particles, was found to be very effective in cleaning solid surfaces such as enamel and porcelain.
  • Cleanser composition A containing the colored particles of the invention, was more effective in cleaning than cleanser B, which did not contain a bleach activator.
  • the cleanser A also had a cleaning ability equal to or better than cleanser C, which contained sodium bromide bleach activator dispersed throughout the composition while in cleanser A it was only in the particles.
  • the colored particles have esthetic appeal, as pointed out above, and are comparable in performance to a bleach activator that is mixed in and distributed throughout a cleanser composition.
  • a colored solid particle consisting essentially of water soluble carrier particles selected from the group consisting of sodium chloride, potassium chloride and sodium sulfate, said carrier particles having coated thereon a mixture consisting essentially of a water soluble alkali metal bromide salt, a water dispersible pigment stable in the presence of hypohalide-liberating bleaching agents and a colorant extender selected from the group consisting of propylene glycol, polyethylene glycol 300 and propylene glycol phenol ether.
  • bleach activator bromide salt is a member selected from the group consisting of sodium bromide, lithium bromide and potassium bromide.
  • a colored solid particle as in claim 1 wherein the colorant extender is propylene glycol.
  • a colored solid particle as in claim 1 having a diameter of0.l5 mm to 2.0 mm.
  • a colored solid particle as claimed in claim 1 further containing at least one member selected from the group consisting of sodium carbonate, tri-sodium phosphate, bora x and tripolyphosphate.
  • a scouring cleanser consisting essentially of the particles of claim I, from 45 to 95 percent by weight of a substantially white colored abrasive selected from 10 hypohalide-liberating bleaching agent and compatible with the remaining ingredients of the scouring composition, from 0.1 to 25 percent by weight of a hypohalide bleaching agent capable of liberating hypochlorite chlorine and/or hypobromite bromine upon contact with aqueous media and from 0 to 95 percent by weight of a builder salt selected from the group consisting of trisodium phosphate, sodium acid pyrophosphate, sodium carbonate, tetra sodium pyrophosphate, sodium tripolyphosphate, sodium sulfate, sodium silicate, so-
  • a scouring cleanser according to claim 7 wherein the detergent is sodium dodecyl benzene sulfonate, the abrasive is silica, the alkali metal bromide is sodium bromide and the hypohalide bleaching agent is trichloro cyanuric acid.
  • composition according to claim 7 wherein said abrasive is silica.
  • a process for preparing the colored solid particle of claim 1 consisting essentially of the steps of;
  • step b adding a colorant extender selected from the group consisting of propylene glycol, polyethylene glycol 300 and propylene glycol phenol ether to the mixture of step b); and
  • step d mixing the product of step c) for about 15 minutes.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Detergent Compositions (AREA)
US00341211A 1971-01-25 1973-03-14 Scouring cleanser composition Expired - Lifetime US3850833A (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
GB302672A GB1378923A (en) 1971-01-25 1972-01-21 Coloured particles and cleanser composition containing same
FR7202191A FR2123356B1 (enExample) 1971-01-25 1972-01-24
CA133,071A CA943428A (en) 1971-01-25 1972-01-24 Colored particles and cleanser composition containing same
DE2203141A DE2203141C3 (de) 1971-01-25 1972-01-24 Gefärbte Teilchen sowie ihre Verwendung in Allzweckreinigungsmitteln
AU38225/72A AU473970B2 (en) 1971-01-25 1972-01-24 Colored particles and cleanser compostion containing same
AT57172A AT319442B (de) 1971-01-25 1972-01-25 Scheuerpulver
NLAANVRAGE7201035,A NL172674C (nl) 1971-01-25 1972-01-25 Werkwijze voor het bereiden van vaste, gekleurde deeltjes, alsmede van was- of schuurmiddelen die deze bevatten.
CH109872A CH569083A5 (enExample) 1971-01-25 1972-01-25
US00341211A US3850833A (en) 1971-01-25 1973-03-14 Scouring cleanser composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10960871A 1971-01-25 1971-01-25
US00341211A US3850833A (en) 1971-01-25 1973-03-14 Scouring cleanser composition

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US3850833A true US3850833A (en) 1974-11-26

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US00341211A Expired - Lifetime US3850833A (en) 1971-01-25 1973-03-14 Scouring cleanser composition

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US (1) US3850833A (enExample)
AT (1) AT319442B (enExample)
AU (1) AU473970B2 (enExample)
CA (1) CA943428A (enExample)
CH (1) CH569083A5 (enExample)
DE (1) DE2203141C3 (enExample)
FR (1) FR2123356B1 (enExample)
GB (1) GB1378923A (enExample)
NL (1) NL172674C (enExample)

Cited By (23)

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US4235599A (en) * 1978-05-30 1980-11-25 Glyco Chemicals, Inc. Bleaching composition
WO1981002313A1 (en) * 1978-05-30 1981-08-20 Glyco Chemicals Inc Low temperature bleaching
US4600406A (en) * 1985-03-22 1986-07-15 Diversey Wyandotte Corporation Method of low temperature bleaching with reduced amounts of chlorine requiring reduced bleaching intervals
US4671886A (en) * 1985-11-25 1987-06-09 The Procter & Gamble Company Process for coloring granular product by admixing with pigment/diluent premix
US4751016A (en) * 1985-02-26 1988-06-14 The Clorox Company Liquid aqueous abrasive cleanser
US4784788A (en) * 1985-12-14 1988-11-15 Colgate-Palmolive Co. Cleaning paste with soluble abrasive
AU629227B2 (en) * 1988-06-30 1992-10-01 Ppg Industries Ohio, Inc. Solid halogen-containing composition and method for producing same
WO1996027651A1 (en) * 1995-03-03 1996-09-12 The Procter & Gamble Company Cleaning compositions with reduced skin malodor
US5714136A (en) * 1991-10-22 1998-02-03 Kao Corporation Hair cosmetic containing a cationic surfactant, fat and oil and an alkyl saccharide surfactant
WO1999051714A3 (en) * 1998-04-07 1999-11-18 Unilever Plc Coloured granular composition for use in particulate detergent compositions
WO2000027980A1 (en) * 1998-11-06 2000-05-18 The Procter & Gamble Company Speckle particles and compositions containing the speckle particles
WO2002010327A1 (en) * 2000-07-31 2002-02-07 Unilever Plc Coloured speckle composition and particulate laundry detergent compositions containing it
US6534471B1 (en) * 1998-01-15 2003-03-18 Henkel Kommanditgesellschaft Auf Aktien Method for producing colored detergents and cleaning agents
US20030104074A1 (en) * 1998-06-01 2003-06-05 Moore Robert M. Concentrated aqueous bromine solutions and their preparation
US20040022874A1 (en) * 1998-06-01 2004-02-05 Nalepa Christopher J. Active bromine containing biocidal compositions and their preparation
US20040219231A1 (en) * 2000-09-08 2004-11-04 Moore Robert M Production of concentrated biocidal solutions
US7172782B2 (en) 2001-06-28 2007-02-06 Albemarle Corporation Microbiological control in poultry processing
US7182966B2 (en) 2001-06-28 2007-02-27 Albemarle Corporation Microbiological control in poultry processing
EP2009086A1 (en) 2007-06-26 2008-12-31 Sociedad Anonima Minera Catalano-Aragonesa (Samca) Procedure for colouring non-adsorbent minerals and the product thus obtained
US20090081317A1 (en) * 2004-12-23 2009-03-26 Albemarle Corporation Microbiocidal Control in the Processing of Meat-Producing Four-Legged Animals
US20090110768A1 (en) * 2003-06-24 2009-04-30 Albemarle Corporation Microbiocidal Control in the Processing of Meat-Producing Four-Legged Animals
US7914365B2 (en) 2005-12-01 2011-03-29 Albemarle Corporation Microbiocidal control in the processing of meat-producing four-legged animals
US8409630B2 (en) 1998-06-01 2013-04-02 Albermarle Corporation Continuous processes for preparing concentrated aqueous liquid biocidal compositions

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ZA804929B (en) * 1979-08-16 1982-03-31 Unilever Ltd Bleach composition
US4464281A (en) * 1983-07-28 1984-08-07 Lever Brothers Company Stabilized bleach-sensitive dyes in automatic dishwasher detergent compositions

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US3503884A (en) * 1966-05-18 1970-03-31 Colgate Palmolive Co Scouring cleanser composition
US3577347A (en) * 1968-04-03 1971-05-04 John Alexander Monick Water-soluble scouring composition

Patent Citations (3)

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Publication number Priority date Publication date Assignee Title
US3503884A (en) * 1966-05-18 1970-03-31 Colgate Palmolive Co Scouring cleanser composition
US3519569A (en) * 1966-05-18 1970-07-07 Colgate Palmolive Co Abrasive scouring cleanser
US3577347A (en) * 1968-04-03 1971-05-04 John Alexander Monick Water-soluble scouring composition

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1981002313A1 (en) * 1978-05-30 1981-08-20 Glyco Chemicals Inc Low temperature bleaching
US4235599A (en) * 1978-05-30 1980-11-25 Glyco Chemicals, Inc. Bleaching composition
EP0046767A4 (en) * 1980-02-11 1982-07-06 Glyco Chemicals Inc BLEACHING PROCEDURE AT LOW TEMPERATURE.
US4751016A (en) * 1985-02-26 1988-06-14 The Clorox Company Liquid aqueous abrasive cleanser
US4600406A (en) * 1985-03-22 1986-07-15 Diversey Wyandotte Corporation Method of low temperature bleaching with reduced amounts of chlorine requiring reduced bleaching intervals
US4671886A (en) * 1985-11-25 1987-06-09 The Procter & Gamble Company Process for coloring granular product by admixing with pigment/diluent premix
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Also Published As

Publication number Publication date
FR2123356B1 (enExample) 1976-07-09
DE2203141C3 (de) 1981-12-24
NL172674C (nl) 1983-10-03
NL7201035A (enExample) 1972-07-27
DE2203141A1 (de) 1972-08-17
NL172674B (nl) 1983-05-02
CA943428A (en) 1974-03-12
CH569083A5 (enExample) 1975-11-14
AT319442B (de) 1974-12-27
FR2123356A1 (enExample) 1972-09-08
AU3822572A (en) 1973-07-26
GB1378923A (en) 1974-12-27
AU473970B2 (en) 1976-07-08
DE2203141B2 (de) 1980-10-09

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