CA1120370A - Liquid bleaching compositions - Google Patents

Liquid bleaching compositions

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Publication number
CA1120370A
CA1120370A CA000321026A CA321026A CA1120370A CA 1120370 A CA1120370 A CA 1120370A CA 000321026 A CA000321026 A CA 000321026A CA 321026 A CA321026 A CA 321026A CA 1120370 A CA1120370 A CA 1120370A
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Prior art keywords
composition
weight
compositions
alkyl sulfate
surfactant
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Expired
Application number
CA000321026A
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French (fr)
Inventor
Harold H. Beyer
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Procter and Gamble Co
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Procter and Gamble Co
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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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395Bleaching agents
    • C11D3/3956Liquid compositions
    • 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • C11D1/143Sulfonic acid esters
    • 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0013Liquid compositions with insoluble particles in suspension
    • 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/1253Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
    • C11D3/1266Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in liquid compositions
    • 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/14Fillers; Abrasives ; Abrasive compositions; Suspending or absorbing agents not provided for in one single group of C11D3/12; Specific features concerning abrasives, e.g. granulometry or mixtures

Abstract

LIQUID BLEACHING COMPOSITIONS

H. H. Beyer ABSTRACT OF THE DISCLOSURE
Alkaline aqueous hypochlorite cleaning compositions containing paraffin sulfonates as bleach stable surfactants.

Description

BACKGROUND AND DESCRIPTION OF PRIOR ART
S This invention relates to liquid detergent bleaching compositions possessing excellent storage stability. The liquid detergent bleaching composition is an alkaline aqueous solution of a compound which produces hypôchlorite ions in aqueous solution, and a paraffin sulfonate surface active agent. In a preferred embodiment, the compositions of the invention have suspended therein, a particulate abrasive material, and have utility as liquid scouring cleansers.
The incorporation of hypochlorite bleach into liquid cleaning compositions, such as scouring cleansers and other types of hard surface cleaners is highly desirable because the hypochlorite is effective in promoting soil and stain removal, and is also an effective disinfectant. However, because of the powerful oxidizing power of hypochlorite bleach, its formulation into liquid cleaning products generally results in chemical instability because of reaction between the bleach and the organic surfactants which are used in such products.

. ~ . ..
' .' : . .
.. . ~ ,. .

il'~0370 U.S. Patent 4,005,027 issued to Hartman January 25, 1977 discloses aqueous li~uid alkaline abrasive scouring compositions comprising a particulate abrasive, a suspending agent for the abrasive, an alkaline buffer salt, hypochlorite bleach and a bleach stable surfactant, alkyl sulfates and betaines being specifically exemplified.

DESCRIPTION OF THE INVENTION
In its broadest aspect the present invention comprises aqueous liquid bleaching compositions comprising from about 0.1~ to about 10% of a compound which produces hypochlorite ions in aqueous media, from about 0.03% to about 10% of a paraffin sulfonate surfactant, from about 1~ to about 20%
of an alkaline salt capable of maintaining said composition at an alkaline pH, and from about 10% to about 90% water.
The compositions can contain various optional ingredients as morc fu~ly described hereinafter. According to the present invention it has been found that the paraffin sulfonate surfactants exhibit a hish degree of chemical stability in the the presence of hypochlorite, and in fact are more stable than the alkyl sulfates disclosed in U.S. Patent 4,005,027. All percentages herein are be weight, lmless otherwise specified.
H ochlorite Bleach YP
Any of the many known compounds which produce the
2~ hypochlorite species (OCl ) in alkaline aqueous solutions can be used as the hypochlorite bleach in the present composi-tions. (See for example U.S. Patent 4,005,027, of H~n, previously mentioned). E~ples of such co~unds include a~i metal and alkaline earth metal hypochlorites, hypochlorite addition products, chloramines, chlorimines, chloramides, ~A 2 -l~Z037U

and chlorimides. S~ecific examples of compounds of these types include sodium hypochlorite, potassium hypochlorite, calcium hypochlorite, magnesium hypochlorite, chlorinated trisodium phosphate dodecahydrate, potassium dichloroiso-cyanurate, sodium dichloroisocyanurate, 1,3-dichloro-5,5-dimethylhydantoin, N-chlorosulfa~ide, Chloramine T, Dichloramine T, Chloramine B and Dichloramine B. A preferred bleaching agent for use in the compositions of the instant invention is sodium hypochlorite.
Most of the above-deseribed hypochlorite-yielding bleaching agents are available in solid or concentrated form and are dissolved in water during preparation of the compositions of the instant invention. Some of the above materials, sueh as sodium hypochlorite, are available as aqueous solutions.
The compounds are present in the compositions at levels of from about 0.1~ to about 10%, preferably from about 0.2% to about 5%.
Surfactant The paraffin sulfonate surfactants, which are an essential ~omponent of the eompositions herein, have the general formula RS03M, wherein R is a primary or secondary alkyl gxoup containing from about 8 to about 22 carbon atoms (preferably 10 to 18) and M is an alkali metal, e.g., sodium or potassium. Paraffin sulfonate surfaetants and methods for their preparation are well known in the art. They may be pre-pared, for example, by reaction of hydrocarbons with sulfur dioxide, oxygen and a sulfonation reaction initiator. Alterna-tively, they may be prepared by reacting an alkene and a sodium bisulfite under suitable radiation or catalysis (See British Patent 1,451,228, published September 29, 1976). Paraffin sul-fonate surfactants are commercially available, e.g., from Farbwerke Hoechst AG.
.

-112~370 Preferred paraffin sulfonates herein are secondary paraffin sulfonates.
Examples of specific paraffin sulfonates herein are:
Sodium-l-decane sulfonate, ~otassium-2-decane sulfonate, Lithium-l-dodecane sulfonate, Sodium-6-tridecane sulfonate, Sodium-2-tetradecane sulfonate, Sodium-l-hexadecane sulfonate, Sodium-4-octadecane sulfonate Sodium-3-octadecane sulfonate.
Normally, the paraffin sulfonates are available as mixtures of individual chain lengths and position isomers, and such mixtures are suitable for use herein.
In addition to excellent chemical stability in the presence of hypochlorite bleach, the paraffin sulfonates are highly effective in removing certain soils (such as greasy food stains) from hard surfaces.
The paraffin sulfonates are moderately low foaming surfactants when used alone in the com~ositions herein. Their foaming power can be boosted by combining them with alkyl sul~ate surfactants of the formula R0503~ wherein R is a primary alkyl group containing from about ~ to about 22 (preferably 10 to 18) carbon atoms and M is an alkali metal, e.g., so~iu~ or potassium. Examples of alkyl sulfates are sodium lauryl sulfate, sodium myristyl sulfate, potassium hexadecyl sulfate, and sodium octadecyl sulfate, coconut alkyl sulfate - and tallow alkyl sulfate.
When used in mixtures herein, the weight ratio of paraffin sulfonate to alkyl sulfate in such mixtures is from about l:lO,to about 10:1 , preferably 1:2 to about 2:1 4 ,~

~Z0370 Such mi~tures provide a synergistic sudsing effect, i.e., the mixtures provide higher sudsing than eithe~ surfactant alone.
Even though alkyl sùlfates are not as stable to hypochlorite as paraffin sulfonates, various mixtures of the two surfactants such as those within the preferred range set forth above appear to be as stable to hypochlorite as paraffin sulfonate alone.
The total surfactant level in compositions of the invention is from about .03~ to about 10%, preferably from about 0.1% to about 5%, regardless of whether paraffin sulfonate or a mixture of paraffin sulfonate and alkyl sulfate is used.

Alkaline Buffer Salt From about 1~ to about 20% by weight, preferably from about 2%to 15% by weight, of the present compositions comprises an inorganic alkaline salt capable of maintaining an alkaline pH in the composition. Preferably the type and amount of alkaline salt is chosen so as to keep the composition pH
within the range of from about 10.0 to 14; preferably from about 10.5 to 13. Maintenance of composition pH at above about 10.0 is an important factor in the maximization of the unique chemical stability of the instant compositions and additionally serves to enhance the cleaning performance of ~he compositions.
Maintenance of the composition pH within the 10.0 to 14 range helps to minimize chemical decomposition of the hypo-2S chlorite-ylelding bleaching agents in aqueous media. Mainten-ance of this pH range also minimizes any chemical interaction between the hypochlorite compound and the paraffin sulfonate surfactant compounds present in the instant compositions.
Finally, high pH values serve to enhance the soil and stain removal properties of the surfactant during utilization of the present compositions.

l~Z0370 Rny bleach-stable salt or mi~ture of salts which has the effect of providing the composition with an alkaline pH
and maintaining it there can be utilized as the alkaline salt in the instant invention (see for example U.S. Patent 4,005,027).
Such materials can include, for example, various water-soluble (i.e., soluble in ~ater to the extent of at least 1% by weight at room temperature), inorganic salts such as the alkali metal (e.g., sodium or potassium) carbonates, bicarbonates, sesquicarbonates, silicates, pyrophosphates, phosphates, tetraborates, and mi~tures thereof. Specific examples of materials which can be used either alone or in combination as the alkaline salt herein include potassium carbonate, sodium bicarbonate, sodium sesquicarbonate, sodium silicate, tetrapotassium pyrophosphate, trisodium phosphate, anhydrous sodium tetraborate, sodium tetraborate pentahydrate, sodium tetraborate decahydrate, and mixtures of these salts.
Preferred alkaline salts for use herein include mixtures of tetrapotassium pyrophosphates and tripotassium phosphate in a pyrophosphate/phosphate salt weight ratio of about 2:1 and mixtures of anhydrous potassium carbonate and sodium bicarbonate in a carbonate/bicarbonate salt~eight ratio of akout 50:1. Txansi-tion metal salts should generally be avoided, since many of these tend to decompose hypochio~ e ions in aqueous media.
Generally, the alkali metal salts are preferred.
It is highly preferred in compositions of the instant invention to include a material which acts as a detergent builder, i.e., a material which reduces the free calcium and/or magnesium ion concentration in a surfactant-containing aqueous sollltion. Some of the above-described alkaline materials additionally serve as builder materials. Such compounds as the caxbonates, phosphates and pyrophosphates are of this type.
Other alkaline materials such as tetraborates perform no ~lZ0370 building function, although they arc still useful h~rein for the alkaline p~l which they provide.
Since presence of a builder in the instant compositions is highly desirable, it is preferred that the essential alkaline salt component of the compositions contains at least one compound capable of acting as a builder, i.e., capable of lowering the free calcium and/or magnesium ion content of an aqueous solution such as is formed by diluting compositions of the present invention with tap water.
Water From about 10% to about 90% by weight, preferably from about 50% to 85% by weight, of the instant composition comprises water. Water is the medium which serves to dissolve the soluble components of the instant invention, for example, the bleach, surfactant, buffering agent and various optional materials. Since it is well known that many transition metals can react with and deactivate the bleaching agets of the present invention, such metals should preferably not be present in the water used to prepare the compositions of thé invention.
Preferably, the water used to prepare the compositions of the invention should be "soft" or deionized water.
Liquid Scouring Compositions Preferred compositions of the present invention are liquid scouring cleansers which contain, in addition to the ~5 essential ingredlents listed hereinbefore, a particulate llZ~3~0 insoluble abrasive and a suspe~ding asent which serves to kee~
the abrasive suspended in the composition. Such compositions are described in detail in U.S. Patents 4,005,027, issued January 25, 1977, 3,985,668, issued October 12, 1976, and 4,051,056, issued September 27, 1977, all issued to Hartma~

The insoluble particulate abrasive material comprises from about 5% to about 60~, preferably from about 8% to about 32~ of the liquid scouring composition. Such insoluble materials have particle size diameters ranging from about 1 to about 250 microns and specific gravities of from about 0.2 to about 5Ø
It is preferred that the diameter of the particles range from about 2 microns to about 190 microns and that their specific gravity range from about 0.3 to about 2.8, most prefera~ly from about 0.4 to 2.4. Insoluble abrasive particulate material of this size and specific gravity can be suspended in the false-body scouring compositions of the type disclosed in the aforedescribed pa-tents issued to Hartman. "Specific gravity"
for purposes of the instant invention has its conventional definition, i.e., the weight of abrasive material per cubic centimeter of water displaced by such material.
The ab-asives which can ~e utilized include, but are ... .. . .
not limited to, quartz, pumice, pumicite, titanium dioxide (TiO2), silica sand, calcium carbonate, zirconium silicate, diatomaceous earth, whiting, feldspar and expanded perlite.
Expanded perlite is the preferred abrasive for these liquid compositions. ~ detailed discussion of expanded perlite and its use in liquid scouring compositions is given in U.S. Patent 4,051,056, supra~

~A `
~ 8 --~ZQ370 Suspending Agent The suspending agents for use in the abrasive-containing compositions herein are the inorganic colloid-forming clays selected from the group consisting of smectites, attapulgites and mixtures of smectites and attapulgites. Smectites are preferred. The clay combines with the free water of the liquid compositions of the present invention to form fluid compositions which are false-bodied in nature.
"False-body" fluids are related to but are not identical to fluids having thixotropic properties. True thixotropic materials break down completely under the influence of high stresses and behave like true liquids even after the stress has been removed, until such time as the structure is reformed.
False-bodied materials, on the other hand, do not, after stress removal, lose their solid properties entirely and can still exhibit a yield value even though it might be diminished. The original yield value is regained only after such fluids are at rest for considerable lengths of time. (See Non-Newtonian Fluids, Wilkinson, Pergamon Press (1960).) The instant preferred false-body liquid compositions in a quiescent state are highly viscous, are Bingham plastic in nature, and have relatively high yield values. When subjected to shear stresses, however, such as being shaken in a bottle or squeezed through an orifice, these preferred compositions fluidize and can be easily dispensed. When the shear stress is stopped, the compositions quickly revert to a high viscosity/Bingham plastic state.
The aforementioned types of clays and their use in ~ormulating false-body fluid scouring cleansers are more fully described in U.S. Patent 4,005,027, supra, 11~0370 The clay suspending agent is generally present in the liquid compositions of the instant invention to the extent of from about 1% to 30~ by weight, preferabl~ from about 2% to 5% by weight, of the total composition.
Miscellaneous Optional Materials In addition to the aforedescribed materials which comprise compositions of the instant invention, such compositions can optionally also contain various other materials to enhance their performance, stability, or aesthetic appeal. Such materials include optional nonbufferina builder compounds, coloring agents and perfumes. Although, as noted above, some of the above-described alkaline salts do function as builder compounds, it is possible to add other bleach-stable builder compounds which are not, in themselves, alkaline salts.
Typical of these optional builder compounds which do not necessarily buffe~ within the required pH range are certain zeolites (See U.S. Patent 3,985,669, Kr~mel e~ al., issued October 12, 1976~, Conventional coloring agents and perfumes can also be added to the instant compositions to enhance their aesthetic appeal and/or consumer acceptability. These materials should, o course, be those dye and perfum.e Yarie~i~s which are especially stable against degradation by strong active chlorine bleaching agents.
If present, the above-described optional materials generally comprise no more than about 5% by weight of the total composition.

Composition Preparation The liquid compositions of the instant invention can be prepared by admixing the above-described essential and optional components together in the appropriate concentrations by conventional means normally used to form the requisite compositions. Some shear agitation is generally necessary to insure proper preparation of such compositions when they contain an abrasive and suspending agent. The extent of shear agitation, in fact, can be used to vary,as desired,the nature of the liquid abrasive compositions so prepared~
A particularly preferred procedure for preparing false-body liquid abrasive compositions is described in Example II of this specification.
Composition Use The liquid compositions of the present invention can be used in a wide variety of cleaning and scouring operations where bleaching and/or disinfecting performance is required.
For example, the nonabrasive compositions herein find use in cleaning and disinfecting of tableware for restaurants and institutions, bleaching of textiles and cleaning of restroom floors and animal cages. The abrasive compositions find use in the scouring of sinks, bathtubs and various other nard surfaces wherein soil accumulates which is difficult to remove by ordinary detersive processes.
The present invention will be illustrated by the following examples.

l~Z0370 EX~MPLE I
A liquid cleaning and disinfecting composition is prepared having the following formula:
Component Wt.%
Sodium hypochlorite 2%
Na paraffin sulfonate 2 Sodium carbonate . 6 Deionized water 90 100%

The composition is prepared by mixing 382 parts of a 5.25% solution of sodium hypochlorite in deionized water with 20 parts of paraffin sulfonate, 30 parts of sodium carbonate and 568 parts of deionized water. This composition has excellent chemical stability in storage and provides excellent cleaning and disinfecting performance.

.' , .

EX~IPLE II
A false-body, hard surface abrasive cleanser of the following composition is prepared:
Component Wt.
"Gelwhite G~*~layl 2.6 Tetrapotassium pyrophosphate 5.8 Tripotassium orthophosphate 2.6 Sodium hypochlorite bleach 0.9 Sodium secondary paraffin 1.5 sulfonate2 Expanded perlite abrasive3 8.0 (Particle size range-10 to 190 microns, specific gravity 1.45 g/cc.
Pigment 92 ppm Perfume . 0.25 Deionized water Balance lOO.OG~
,.
Composition pH = 11.5 A smectite clay from Southern Clay Co.
2Hostaspur SAS 60 from Farbwerke Hoechst AG
3From Silbrico Co.

* Trademark ** Trademark The above described Example II composition is prepared in the following manner. The clay and about 75~
of the total amount of water used in the formula are mixed together and passed seven times through an in-line high shear mixer to form a uniform aqueous dispersion of the clay. The perlite abrasive is then added. Then the pyrophosphate is mixed slowly into this dispersion to form a false-body fluid.
The remaining ingredients are then added (with mixing) in the order: tripotassium phosphate, pigment, perfume, paraffin sulfonate and sodium h~hlorite. The remainder of the water is ~hen added to make up 100 parts of finished composition, and the composition is passed through a vacuum deaerator to remove entrapped air.
The resulting scouring composition is false-bodied, i.e., gel-like in its quiescent state but easily fluidized by application of shear stress. In its quiescent sta~e, the composition maintains the perlite abrasive in a uniformly suspended dispersion. When applied to horizontal or vertical hard surfaces, the composition is not fluid and does not appreciably run along such surfaces.
~0 Such a composition exhibits negligible clear layer separation and has excellent bleach and surfactant stability in storage. This composition, used in undiluted form, is effective for removal of stains and soil from hard surfaces and in sanitizing the surfaces.

WHAT I S CLAIMED I S:

Claims (10)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. An aqueous false-body hard-surface scouring cleanser consisting essentially of:
A. from about 0.2% to 5% by weight of a bleaching agent which yields hypochlorite ion in aqueous solution;
B. from about 1% to 30% by weight of an inorganic colloid-forming clay selected from the group consisting of smectites, attapulgites and mixtures of smectites and attapulgites;
C. from about 0.1% to 5% by weight of a paraffin sul-fonate surfactant of the formula RSO3M wherein R
is a primary or secondary alkyl group containing from about 8 to about 22 carbon atoms and M is an alkali metal;
D. from about 5% to about 60% by weight of insoluble particulate abrasive material which has particle diameters ranging from one micron to about 250 microns and a specific gravity of from about 0.2 to about 5.0;
E. from about 2% to about 15% by weight of an inorganic alkaline buffer salt capable of maintaining composition pH within the range of from about 10.0 to 14; and F. from about 10% to about 90% by weight of water.
2. The composition of Claim 1, wherein the bleaching agent which produces hypochlorite ion is sodium hypochlorite and is present at a level of from about 0.2% to about 5%, wherein the amount of water in the composition is from about 50% to about 85%, and wherein the amount of abrasive in the composition is from about 8% to about 32%.
3. The composition of Claim 2, wherein the inorganic colloid-forming clay is a smectite clay and is present at a level of from about 2% to about 5% of the composition.
4. The composition of Claim 3 wherein the paraffin sulfonate surfactant is a C10 to C18 paraffin sulfonate.
5. The composition of Claim 4, wherein the inorganic alkaline buffer salt is selected from the group consisting of alkali metal carbonates, bicarbonates, sesquicarbonates, silicates, pyrophosphates, phosphates, tetraborates and mixtures thereof.
6. The composition of Claim 5, wherein the insoluble particulate abrasive is selected from the group consisting of quartz, pumice, pumicite, titanium dioxide, silica sand, calcium carbonate, zirconium silicate, diatomaceous earth, whiting, feldspar, and expanded perlite.
7. The composition of Claim 6, wherein the insoluble particulate abrasive has a specific gravity of from about 0.4 to about 2.4.
8. The composition of Claim 7 wherein the particulate abrasive is expanded perlite.
9. The composition of Claim 4, containing as an additional surfactant a C8 to C22 alkyl sulfate, wherein the ratio of paraffin sulfonate to alkyl sulfate is from 10:1 to about 1:10, and wherein the total surfactant level in the composition is from about 0.1% to about 5%.
10. The composition of Claim 9, wherein the alkyl sulfate is a C10 to C18 alkyl sulfate and wherein the ratio of paraffin sulfonate to alkyl sulfate is from about 1:2 to about 2:1.
CA000321026A 1978-02-08 1979-02-07 Liquid bleaching compositions Expired CA1120370A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US875,954 1978-02-08
US05/875,954 US4235732A (en) 1978-02-08 1978-02-08 Liquid bleaching compositions

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Publication Number Publication Date
CA1120370A true CA1120370A (en) 1982-03-23

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EP (1) EP0003625A1 (en)
JP (1) JPS54148006A (en)
BE (1) BE50T1 (en)
CA (1) CA1120370A (en)
DE (1) DE2948924A1 (en)
FR (1) FR2443496A1 (en)
NL (1) NL7915005A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4599186A (en) * 1984-04-20 1986-07-08 The Clorox Company Thickened aqueous abrasive scouring cleanser
US4657692A (en) * 1984-04-20 1987-04-14 The Clorox Company Thickened aqueous abrasive scouring cleanser

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0030096B2 (en) * 1979-12-04 1993-07-14 Imperial Chemical Industries Plc Detergent composition
DE3163411D1 (en) * 1980-10-16 1984-06-07 Unilever Nv Stable liquid detergent suspensions
SE453834B (en) * 1982-01-18 1988-03-07 Colgate Palmolive Co GEL TYPE COMPOSITION WITH TIXOTROPIC PROPERTIES INTENDED FOR AUTOMATIC DISHWASHERS
US4388204A (en) * 1982-03-23 1983-06-14 The Drackett Company Thickened alkali metal hypochlorite compositions
DE3246080A1 (en) * 1982-12-13 1984-06-14 Henkel KGaA, 4000 Düsseldorf CLEANING PROCEDURE
GB8325541D0 (en) * 1983-09-23 1983-10-26 Unilever Plc Liquid thickened bleaching composition
JPS60124700A (en) * 1983-12-12 1985-07-03 ミマス油脂化学株式会社 Bleaching agent with viscosity
US4623476A (en) * 1984-03-30 1986-11-18 The Procter & Gamble Company Stable suspension of pigments in aqueous hypochlorite bleach compositions
FR2570713B1 (en) * 1984-09-21 1987-08-21 Lesieur Cotelle THICK AQUEOUS CLEANING COMPOSITIONS
US5213705A (en) * 1985-04-30 1993-05-25 Ecolab Inc. Encapsulated halogen bleaches and methods of preparation and use
JPS62285999A (en) * 1986-06-02 1987-12-11 マツダ株式会社 Fungicidal agent on film
US4772414A (en) * 1986-07-24 1988-09-20 Ppg Industries, Inc. Bleaching composition
US5139695A (en) * 1988-01-14 1992-08-18 Ciba-Geigy Corporation Stable bleaching compositions containing fluorescent whitening agents
US4842757A (en) * 1988-01-21 1989-06-27 The Clorox Company Thickened liquid, improved stability abrasive cleanser
AU626836B2 (en) * 1988-04-01 1992-08-13 Clorox Company, The Thickened pourable aqueous cleaner
US5298181A (en) * 1988-04-01 1994-03-29 The Clorox Company Thickened pourable aqueous abrasive cleanser
US5236614A (en) * 1990-09-25 1993-08-17 Colgate-Palmolive Company Stable microemulsion disinfecting detergent composition
AU7723494A (en) * 1993-09-20 1995-04-10 Procter & Gamble Company, The Use of hypochlorite-comprising compositions with a short chain surfactant for odour reduction
US5843190A (en) * 1993-11-11 1998-12-01 The Procter & Gamble Company Hypochlorite bleaching compositions
EP0892042A1 (en) * 1993-11-11 1999-01-20 The Procter & Gamble Company The use of silicates in hypochlorite bleaching compositions
ATE190647T1 (en) * 1993-11-11 2000-04-15 Procter & Gamble HYPOCHLORITE BLEACH COMPOSITION
US5914069A (en) * 1993-11-11 1999-06-22 The Procter & Gamble Company Hypochlorite bleaching compositions
EP0767828B1 (en) * 1994-06-27 1998-10-21 Unilever N.V. Detergent composition
GB2305434B (en) * 1995-09-19 1999-03-10 Reckitt & Colmann Sa Abrasive cleaning composition
US5679877A (en) * 1996-06-14 1997-10-21 Colgate-Palmolive Co. Thickened liquid cleaning composition containing an abrasive
RU2130964C1 (en) * 1998-02-10 1999-05-27 Оганесов Владимир Емельянович Aqueous disinfectant solution
US20040101881A1 (en) * 2002-02-01 2004-05-27 Gerard Durmowicz Surfactant/oxidizing agent solution and methods of use
CA2615253C (en) * 2005-07-12 2011-03-15 Stepan Company Composition and method for deactivating allergenic proteins on surfaces
EP2719752B1 (en) * 2012-10-15 2016-03-16 The Procter and Gamble Company Liquid detergent composition with abrasive particles
EP3196282B1 (en) * 2013-12-23 2021-03-03 Imertech Sas Cleansing compositions
EP3040408A1 (en) 2014-12-31 2016-07-06 Hayata Kimya Sanayi Anonim Sirketi Aqueous liquid cleaning compositions comprising bleaching agent and abrasive particles

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3172861A (en) * 1965-03-09 Hypochlorite bleaching compositions
ZA674667B (en) * 1966-08-11
FR2094708A5 (en) 1970-06-30 1972-02-04 Moreau Francis Foamed javel water-contg a detergent
JPS4926688B1 (en) * 1970-12-09 1974-07-11
US4005027A (en) * 1973-07-10 1977-01-25 The Procter & Gamble Company Scouring compositions
JPS565800B2 (en) * 1973-12-11 1981-02-06
US4051056A (en) * 1974-09-09 1977-09-27 The Procter & Gamble Company Abrasive scouring compositions
LU71583A1 (en) * 1975-01-02 1976-11-11 Procter & Gamble Europ
US4071463A (en) * 1975-09-11 1978-01-31 The Dow Chemical Company Stable cleaning agents of hypochlorite bleach and detergent
US4051055A (en) * 1976-12-21 1977-09-27 The Procter & Gamble Company Cleansing compositions
US4116849A (en) * 1977-03-14 1978-09-26 The Procter & Gamble Company Thickened bleach compositions for treating hard-to-remove soils

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4599186A (en) * 1984-04-20 1986-07-08 The Clorox Company Thickened aqueous abrasive scouring cleanser
US4657692A (en) * 1984-04-20 1987-04-14 The Clorox Company Thickened aqueous abrasive scouring cleanser

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DE2948924A1 (en) 1980-05-08
EP0003625A1 (en) 1979-08-22
NL7915005A (en) 1980-05-30
JPS54148006A (en) 1979-11-19
US4235732A (en) 1980-11-25
FR2443496A1 (en) 1980-07-04
BE50T1 (en) 1980-04-11

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