US3458446A - Abrasive scouring cleanser - Google Patents

Abrasive scouring cleanser Download PDF

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Publication number
US3458446A
US3458446A US550967A US55096766A US3458446A US 3458446 A US3458446 A US 3458446A US 550967 A US550967 A US 550967A US 55096766 A US55096766 A US 55096766A US 3458446 A US3458446 A US 3458446A
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US
United States
Prior art keywords
abrasive
weight
bromide
water
salts
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
US550967A
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English (en)
Inventor
Ramon Bruno Diaz
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
Original Assignee
Colgate Palmolive Co
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 to CA813300A priority Critical patent/CA813300A/en
Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co
Priority to US550967A priority patent/US3458446A/en
Priority to SE6629/67A priority patent/SE324201B/xx
Priority to DE19671669103 priority patent/DE1669103A1/de
Priority to GR670133404A priority patent/GR33404B/el
Priority to AU21867/67A priority patent/AU420400B2/en
Priority to FR106665A priority patent/FR1523009A/fr
Priority to ES340631A priority patent/ES340631A1/es
Priority to CH697267A priority patent/CH493626A/de
Priority to JP42030934A priority patent/JPS4830323B1/ja
Priority to AT460967A priority patent/AT270429B/de
Priority to GB22967/67A priority patent/GB1185214A/en
Priority to BE698583D priority patent/BE698583A/xx
Priority to NL6706854A priority patent/NL6706854A/xx
Application granted granted Critical
Publication of US3458446A publication Critical patent/US3458446A/en
Priority to MY293/73A priority patent/MY7300293A/xx
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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/046—Salts
    • 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
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39—Organic or inorganic per-compounds
    • C11D3/3942—Inorganic per-compounds
    • 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
    • C11D3/3953—Inorganic bleaching agents
    • 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
    • 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
    • C11D3/3958—Bleaching agents combined with phosphates

Definitions

  • This invention relates to abrasive scouring cleansers. More particularly, it relates to abrasive scouring cleansers of the type which contain monopersulfates as bleaching and oxidizing constituents.
  • abrasive scouring cleansers which contain monopersulfate oxidizing agents is substantially benefited by the inclusion in such compositions of a small amount of a water-soluble bromide salt.
  • the abrasive scouring cleansers of the instant invention are characterized by highly rapid and complete stain and soil removal, oxidizing and disinfecting action. This action appears to be substantially greater than is achieved by comparable chloride salts.
  • the instant compositions are characterized (when unperfumed) by a pleasant odor which is relatively non-irritating, both on use with water and with respect to residual odor effects on the hands of users.
  • hypochlorites or chlorine liberating constituents such an water-soluble chloride salts
  • the instant compositions are characterized (when unperfumed) by a pleasant odor which is relatively non-irritating, both on use with water and with respect to residual odor effects on the hands of users.
  • hypochlorites from the instant cleansers also facilitates perfuming thereof by conventional essential oils and perfumery constituents.
  • these improved compositions are highly stable on storage and eificacious in polishing tarnished metal surfaces and in removal of smears or deposits of soft materials such as aluminum on porcelain surfaces.
  • an abrasive scouring cleanser comprises at least about 60% by weight of a Water-insoluble inorganic siliceous abrasive material having a particle size (diameter) of less than about 0.5 mm., about 0.1 to 20% by weight of an alkali metal monopersulfate salt, about 0.5 to 15% by weight of a water-soluble organic detergent compound substantially stable in the presence of said monopersulfate salt, and about 0.1 to 10% by weight of a water-soluble bromide salt.
  • the abrasive agents of the scouring cleansers of the present invention include siliceous materials such as silica, feldspar, pumice, vulcanic ash, diatomaceous earth, bentonite and talc, and mixtures thereof.
  • silica or feldspar of various degrees of fineness for they are relatively hard and result in a whiter product.
  • the abrasives may vary in hardness, particle size and shape, and the choice for a particular composition is generally dependent upon the contemplated field of application.
  • the particle size of the abrasive is less than 0.5 mm. and in general, the maximum particle size of substantially all of the abrasive is about 0.15 mm. Normally the abrasive employed will have a particle size such that at least about 85% and preferably 99% by Weight thereof passes through a sieve having 0.074
  • abrasive particles in the interest of effecice tive cleansing action, it is appropriate for at least about 8% by weight of the abrasive particles to have a diameter of about 0.037 mm. or larger.
  • the abrasive is present in a proportion of at least about 60%, and preferably at least about to by weight of the cleanser.
  • the alkali metal monopersulfate salts of the instant compositions preferably are the potassium or sodium salts, which are commercially available.
  • the potassium salt is most preferred and may, if desired, be employed in the form of a triple salt with potassium bisulfate and potassium sulfate, e.g., KHSO KHSO -K SO in the mole ratio of about 221:1.
  • the third essential ingredient of the present novel abrasive cleansers is a water-soluble organic detergent which is stable in the presence of the contemplated hypochlorite-liberating component.
  • organic detergents may be anionic, cationic, amphoteric or non-ionic in character, provided that they are compatible with the compositions as a whole in the proportions employed. Where they are liquids under normal conditions, such as the non-ionic agents generally, they may be prepared in particular solid form after absorption upon diatomaceous earth or other similar agents in procedures Well known in the art.
  • suitable anionic detersive compounds contemplated within the ambit of the invention are the soaps and the sulfated and sulfonated synthetic detergents, especially those anionic detergents having about 8 to about 26 and perferably about 12 to about 22 carbon atoms to the molecule.
  • the soaps are generally the watersoluble salts of saturated higher fatty acids and mixtures thereof.
  • the sulfated and sulfonated detersive compounds are also well-known in the art and may be prepared from suitable organic materials which are applicable to sulfonation (true sulfonation and/or sulfation). Of the vast variety of sulfates and sulfonates suitable, it is preferred to use the aliphatic sulfates and sulfonates of about 8 to 22 carbon atoms and the alkyl aromatic sulfonates.
  • the alkyl aromatic sulfonate detergents referred to may be mononuclear or polynuclear in structure. More particularly, the aromatic nucleus may be derived from benzene, toluene, xylene, phenol, cresols, phenol ethers, naphthalene, derivatives of phenanthrene nuclei, etc. It has also been found that the alkyl group may vary similarly.
  • the alkyl groups may be straight or branch chained and may consist of such radicals as dodecyl, pentadecyl, octyl, nonyl, decyl, keryl, mixed alkyls derived from fatty materials, cracked paraffin wax olefins and polymers of lower mono olefins, etc. While the number of sulfonic acid groups present on the nucleus may vary, it is usual to have only one such group present in order to preserve as much as possible a balance between hydrophilic and hydrophobic portions of the molecule.
  • alkyl aromatic sulfonate detergents are the propylated naphthalene sulfonates, the mixed butyl naphthalene sulfonates, tetrahydronaphthalene sulfonates, the various butylated diphenyl sulfonates and phenyl-phenol sulfonates. It is preferred, however, to use the higher alkyl aromatic sulfonates rather than the lower alkyl substituted detergents.
  • Typical examples of this preferred class are the sulfonated and alkylated benzene type compounds wherein the alkyl group is at least 8 and preferably about 10 to about 16 carbon atoms. The benzene ring may possess other substituents including alkyl and hydroxy groups.
  • Suitable agents are the surface-active sulfated or sulfonated aliphatic compounds, preferably having 8-22 carbon atoms.
  • sulfuric acid esters of polyhydric alcohols incompletely esterified with higher fatty acids e.g., coconut oil monoglyceride monosulfate, tallow diglyceride monosulfate; the long chain pure or mixed alkyl sulfates, e.g., lauryl sulfate, cetyl sulfate; the hydroxy sulfonated higher fatty acid esters, e.g., higher fatty acid esters of low molecular weight alkylol sulfonic acids, e.g., fatty acid esters of isethionic acid; the fatty acid ethanolamide sulfates; the fatty acid amides of amino alkyl sulfonic acids, e.g., lauric amide of taurine, and the like. More particularly,
  • anionic detergents are preferred, cationic, non-ionic and amphoteric detergents may be also employed in whole or as part of the detergent component, provided they are compatible with the other elements of the composition under conditions of storage and use thereof.
  • cationic detergents there may be noted the long chain alkyl quaternary ammonium compounds, e.g., cetyl quaternary ammonium salts. Within this group are included cetyl tri-methyl ammonium sulfate and cetyl pyridinium sulfate.
  • Another equivalent cationic agent is the diethylene amino ethyl oleyl amide product.
  • the nonionic agents are also well-known in the art including the polyoxyethylene ethers of alkyl aromatic hydroxy bodies (e.g., the alkylated polyoxyethylene phenols), the polyoxyethylene ethers of long chain aliphatic alcohols, the polyoxyethylene ethers of hydrophobic propylene oxide polymers, and higher alkyl amine oxides such as lauryl dimethyl amine oxide.
  • alkyl aromatic hydroxy bodies e.g., the alkylated polyoxyethylene phenols
  • polyoxyethylene ethers of long chain aliphatic alcohols e.g., the alkylated polyoxyethylene phenols
  • the polyoxyethylene ethers of hydrophobic propylene oxide polymers e.g., the polyoxyethylene ethers of hydrophobic propylene oxide polymers
  • higher alkyl amine oxides such as lauryl dimethyl amine oxide.
  • Amphoteric detergents which also are contemplated, examples thereof including the salts of higher alkyl beta amino propionic acids, e.g., sodium N-lauryl beta alanine; the higher alkyl substituted betaines such as lauryl dimethylammonium acetic acid; and the imidazoline type exemplified by the disodium salt of 1-(2 hydroxyethyl)-1-(carboxymethyl)- 2-(hendecyl)-4,5 dihydroimidazolinium hydroxide.
  • higher alkyl beta amino propionic acids e.g., sodium N-lauryl beta alanine
  • the higher alkyl substituted betaines such as lauryl dimethylammonium acetic acid
  • imidazoline type exemplified by the disodium salt of 1-(2 hydroxyethyl)-1-(carboxymethyl)- 2-(hendecyl)-4,5 dihydroimidazolinium hydroxide.
  • the anionic and cationic surface active agents are commonly used in the form of their water-soluble salts.
  • the alkali metal (e.g. sodium, potassium) salts are preferred, though other salts such as ammonium amine, alkylolamine, and alkaline earth metals (e.g. calcium, magnesium) salts may be used if desired.
  • the cationic agents the chloride, sulfate, acetate and like salts may be employed satisfactorily.
  • the amount of organic detergent to be used in the present compositions is from about 0.5% up to about 15% by weight, and preferably from about 1% to about 5%.
  • Commercial detergent compositions in which these organic detergents are the active ingredients and are compounded with other materials including sodium sulfate, the various phosphates, etc. may be employed with satisfactory results.
  • the bromide salt of the instant compositions is a solid, water-soluble bromide which preferably is of substantially neutral or slightly alkaline nature, providing a ready source of bromide ions on dissolution in water. It is preferred to employ alkali metal bromides such as sodium bromide, sodium bromide dihydrate, lithium bromide and potassium bromide, although alkaline earth metal bromides such as strontium bromide and magnesium bromide may also be employed in those instances in which these water hardness-producing cations are not objectionable.
  • the preferred bromides are anhydrous.
  • the bromide is employed in a proportion of about 0.1% to by weight of the product.
  • Suitable various adjuvant materials may also be used in the instant abrasive detersive compositions. These additives may be inorganic or organic in structure and may be included in compositions of the present invention.
  • Inorganic water-soluble alkaline builders such as the alkali metal silicates, nitrates, carbonates, bicarbonates, phosphates and borates may be added in any suitable amounts, usually up to about 25% and preferably up to about Examples of such builders include sodium carbonate, sodium bicarbonate, sodium metasilicate, trisodium phosphate, tetrasodium pyrophosphate, sodium tripolyphosphate and the corresponding potassium salts.
  • sequestering agents such as nitrilotriacetic acid, ethylene diamine tetracetic acid, diethylene triamine pentaacetic acid and their salts (e.g. sodium salts), wood pulp, sawdust, magnesite, whiting, sodium carboxymethylcellulose, anti-caking agents, optical brighteners, and the like.
  • Silica (at least 88% by weight passes through a wire sieve in which the opening between the wires are 0.074 mm.) 86.1
  • Silica (at least 99% by weight passes through wire sieve in which the openings between the wires are 0.074 mm.) 80.0
  • An abrasive scouring cleanser consisting essentially of at least 60% by weight of a water-insoluble, inorganic, siliceous abrasive material having a particle size of less than about 0.5 him, about 0.1 to 20% by weight of an alkali metal monopersulfate salt, about 0.5 to 15% by weight of a water-soluble organic detergent compound substantially stable in the presence of said monopersulfate salt, and about 0.1 to 10% by weight of a water-soluble salt selected from the group consisting of alkali metal and alkaline earth metal bromide salts.
  • An abrasive scouring cleanser as set forth in claim 1 which contains at least by weight of silica as the inorganic siliceous abrasive material.
  • An abrasive scouring cleanser as set forth in claim 1 which is free of water-soluble chloride salts which react with alkali metal monopersulfatcs to form hypochlorites.
  • An abrasive scouring cleanser which consists essentially of at least about 60% by weight of a water-insoluble inorganic siliceous abrasive material having a particle size of less than about 0.15 mm. and such that at least 85% by weight thereof passes through a sieve having 0.074 mm. openings, about 0.2 to 15% by weight of potassium monopersulfate, about 1 to 5% by weight of a watersoluble anionic organic detergent compound substantially stable in the presence of said potassium monopersulfate, and 0.1 to 10% by weight of sodium bromide.
  • An abrasive scouring cleanser which consists essentially of about 86.1% by Weight of silica having a particle size of less than about 0.15 mm. and such that at least 85% by weight thereof passes through a sieve having 0.074 mm. openings, about 1.0% of a mixture of po- References Cited UNITED STATES PATENTS 8/ 1967 Puetzer et al 25299 FOREIGN PATENTS 4/1960 Great Britain.

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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)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
US550967A 1966-05-18 1966-05-18 Abrasive scouring cleanser Expired - Lifetime US3458446A (en)

Priority Applications (15)

Application Number Priority Date Filing Date Title
CA813300A CA813300A (en) 1966-05-18 Abrasive scouring cleanser
US550967A US3458446A (en) 1966-05-18 1966-05-18 Abrasive scouring cleanser
SE6629/67A SE324201B (ref) 1966-05-18 1967-05-11
DE19671669103 DE1669103A1 (de) 1966-05-18 1967-05-16 Scheuermittel
GB22967/67A GB1185214A (en) 1966-05-18 1967-05-17 Abrasive Scouring Cleansers
FR106665A FR1523009A (fr) 1966-05-18 1967-05-17 Nouveau produit à récurer abrasif
ES340631A ES340631A1 (es) 1966-05-18 1967-05-17 Un metodo para la fabricacion de limpiadores abrasivos parafregar.
CH697267A CH493626A (de) 1966-05-18 1967-05-17 Scheuermittel
GR670133404A GR33404B (el) 1966-05-18 1967-05-17 Μεσον καθαρισμου, στιλβωσεως και αποξεσεως.
AT460967A AT270429B (de) 1966-05-18 1967-05-17 Scheuermittel
AU21867/67A AU420400B2 (en) 1966-05-18 1967-05-17 Abrasive scouring cleanser
BE698583D BE698583A (ref) 1966-05-18 1967-05-17
NL6706854A NL6706854A (ref) 1966-05-18 1967-05-17
JP42030934A JPS4830323B1 (ref) 1966-05-18 1967-05-17
MY293/73A MY7300293A (en) 1966-05-18 1973-12-30 Abrasive scouring cleansers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US550967A US3458446A (en) 1966-05-18 1966-05-18 Abrasive scouring cleanser

Publications (1)

Publication Number Publication Date
US3458446A true US3458446A (en) 1969-07-29

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US550967A Expired - Lifetime US3458446A (en) 1966-05-18 1966-05-18 Abrasive scouring cleanser

Country Status (15)

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US (1) US3458446A (ref)
JP (1) JPS4830323B1 (ref)
AT (1) AT270429B (ref)
AU (1) AU420400B2 (ref)
BE (1) BE698583A (ref)
CA (1) CA813300A (ref)
CH (1) CH493626A (ref)
DE (1) DE1669103A1 (ref)
ES (1) ES340631A1 (ref)
FR (1) FR1523009A (ref)
GB (1) GB1185214A (ref)
GR (1) GR33404B (ref)
MY (1) MY7300293A (ref)
NL (1) NL6706854A (ref)
SE (1) SE324201B (ref)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3715314A (en) * 1971-04-02 1973-02-06 Procter & Gamble Scouring cleanser composition
US4028263A (en) * 1973-08-24 1977-06-07 Colgate-Palmolive Company Bleaching and brightening detergent composition
US4051056A (en) * 1974-09-09 1977-09-27 The Procter & Gamble Company Abrasive scouring compositions
US4116878A (en) * 1974-06-14 1978-09-26 Lever Brothers Company Detergent composition
US4123376A (en) * 1973-08-24 1978-10-31 Colgate-Palmolive Company Peroxymonosulfate-base bleaching and bleaching detergent compositions
US4300897A (en) * 1973-08-24 1981-11-17 Colgate-Palmolive Company Method for bleaching with peroxymonosulfate-based compositions
US4362639A (en) * 1981-04-03 1982-12-07 Warner-Lambert Company Cleanser with improved afterodor and tarnish resistance
US4405486A (en) * 1981-08-31 1983-09-20 Warner-Lambert Company Method for preparing granulated perborate salts containing a polymeric fluorocarbon
US4409118A (en) * 1981-04-03 1983-10-11 Warner-Lambert Company Tablet forming cleanser composition and method of preparation
US4613332A (en) * 1984-07-11 1986-09-23 The Clorox Company Controlled generation hypochlorite compositions and method
US4618444A (en) * 1984-09-17 1986-10-21 Purex Corporation Household laundry detergent with dual strength bleach
EP0271189A3 (en) * 1986-11-03 1989-05-24 The Clorox Company Aqueous acidic hard surface cleaner
US4895669A (en) * 1986-11-03 1990-01-23 The Clorox Company Aqueous based acidic hard surface cleaner
EP0265709A3 (en) * 1986-10-25 1990-07-11 Laporte Industries Limited A method and composition for the treatment of bathtubs

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ITRC20130002A1 (it) * 2013-02-05 2013-05-07 Martelli Giancarlo Nuovo sistema per la produzione di radicali liberi reattivi in assenza di catalizzatori, con attivita' riducente, e suo impiego per la disinfezione e/o sterilizzazione di dispositivi medici immergendoli nella sua soluzione.

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB832105A (en) * 1957-08-30 1960-04-06 Victor John Albericci Improvements in or relating to cleansing and sterilising compositions
US3337466A (en) * 1964-02-15 1967-08-22 Revlon Effervescent dental cleaner compositions

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB832105A (en) * 1957-08-30 1960-04-06 Victor John Albericci Improvements in or relating to cleansing and sterilising compositions
US3337466A (en) * 1964-02-15 1967-08-22 Revlon Effervescent dental cleaner compositions

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3715314A (en) * 1971-04-02 1973-02-06 Procter & Gamble Scouring cleanser composition
US4028263A (en) * 1973-08-24 1977-06-07 Colgate-Palmolive Company Bleaching and brightening detergent composition
US4123376A (en) * 1973-08-24 1978-10-31 Colgate-Palmolive Company Peroxymonosulfate-base bleaching and bleaching detergent compositions
US4300897A (en) * 1973-08-24 1981-11-17 Colgate-Palmolive Company Method for bleaching with peroxymonosulfate-based compositions
US4116878A (en) * 1974-06-14 1978-09-26 Lever Brothers Company Detergent composition
US4051056A (en) * 1974-09-09 1977-09-27 The Procter & Gamble Company Abrasive scouring compositions
US4362639A (en) * 1981-04-03 1982-12-07 Warner-Lambert Company Cleanser with improved afterodor and tarnish resistance
US4409118A (en) * 1981-04-03 1983-10-11 Warner-Lambert Company Tablet forming cleanser composition and method of preparation
US4405486A (en) * 1981-08-31 1983-09-20 Warner-Lambert Company Method for preparing granulated perborate salts containing a polymeric fluorocarbon
US4613332A (en) * 1984-07-11 1986-09-23 The Clorox Company Controlled generation hypochlorite compositions and method
US4618444A (en) * 1984-09-17 1986-10-21 Purex Corporation Household laundry detergent with dual strength bleach
EP0265709A3 (en) * 1986-10-25 1990-07-11 Laporte Industries Limited A method and composition for the treatment of bathtubs
EP0271189A3 (en) * 1986-11-03 1989-05-24 The Clorox Company Aqueous acidic hard surface cleaner
US4895669A (en) * 1986-11-03 1990-01-23 The Clorox Company Aqueous based acidic hard surface cleaner

Also Published As

Publication number Publication date
AU2186767A (en) 1968-11-21
GR33404B (el) 1967-11-30
SE324201B (ref) 1970-05-25
FR1523009A (fr) 1968-04-02
NL6706854A (ref) 1967-11-20
GB1185214A (en) 1970-03-25
AU420400B2 (en) 1972-01-14
DE1669103A1 (de) 1971-04-01
CH493626A (de) 1970-07-15
MY7300293A (en) 1973-12-31
ES340631A1 (es) 1968-10-16
AT270429B (de) 1969-04-25
CA813300A (en) 1969-05-20
BE698583A (ref) 1967-11-03
JPS4830323B1 (ref) 1973-09-19

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