GB2278124A - Detergent composition - Google Patents

Detergent composition Download PDF

Info

Publication number
GB2278124A
GB2278124A GB9310155A GB9310155A GB2278124A GB 2278124 A GB2278124 A GB 2278124A GB 9310155 A GB9310155 A GB 9310155A GB 9310155 A GB9310155 A GB 9310155A GB 2278124 A GB2278124 A GB 2278124A
Authority
GB
United Kingdom
Prior art keywords
weight
bar
water
alcohol
bar according
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.)
Withdrawn
Application number
GB9310155A
Other versions
GB9310155D0 (en
Inventor
Peter James Powers
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.)
Unilever PLC
Original Assignee
Unilever PLC
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
Application filed by Unilever PLC filed Critical Unilever PLC
Priority to GB9310155A priority Critical patent/GB2278124A/en
Publication of GB9310155D0 publication Critical patent/GB9310155D0/en
Priority to IN216BO1994 priority patent/IN182011B/en
Priority to MYPI9401221 priority patent/MY118466A/en
Publication of GB2278124A publication Critical patent/GB2278124A/en
Withdrawn legal-status Critical Current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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/2017Monohydric alcohols branched
    • C11D3/202Monohydric alcohols branched fatty or with at least 8 carbon atoms in the alkyl chain
    • 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
    • C11D1/37Mixtures of compounds all of which are anionic
    • 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
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/0065Solid detergents containing builders
    • C11D17/0069Laundry bars
    • 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
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/201Monohydric alcohols linear
    • C11D3/2013Monohydric alcohols linear fatty or with at least 8 carbon atoms in the alkyl chain
    • 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
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/2017Monohydric alcohols branched
    • 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
    • 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
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds

Landscapes

  • 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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)

Abstract

Built non-soap detergent bars suitable for the laundering of fabrics or cleaning of hard surfaces - containing 5% to 60% by weight of builder and 10% to 60% by weight of non-soap anionic detergent, at least a majority of which is C8 to C18 alkyl benzene sulphonate, C8 to C18 alkyl sulphate or a mixture of the two - is characterised by including 0.3% to 10% by weight of C8 to C24 branched-chain or secondary alcohol. This reduces the formation of soft mush when bars are left in contact with water.

Description

DETERGENT COMPOSITION This invention relates to built, non-soap detergent bars which are used in some countries for the laundering of fabrics and also the cleaning of hard surfaces.
A number of properties are regarded as significant for satisfactory bars. One property concerns the behaviour of a bar when left standing in water. It is undesirable that the outer part of the bar should break up and be lost. It is also undesirable that the outer part of a bar should turn into a soft layer - referred to as mush - which can then be removed by rubbing or scraping.
On the contrary, satisfactory bars should retain their integrity when in contact with water, without however being so hard that the bar composition does not rub off onto fabrics when used.
In US Patent 5,089,174 it is contended that the formation of mush is a problem in bars which contain a mixture of alkylbenzene sulphonate and alkyl sulphate as detergent.
The proposed solution to this problem, set out in this prior patent, is to incorporate into the bar composition a fatty alcohol containing 10 to 22 carbon atoms. Only primary alcohols are mentioned, chiefly of natural origin. All natural fatty alcohols and many synthetic fatty alcohols have unbranched, linear carbon chains containing an even number of carbon atoms.
We have now found that branched chain alcohols and secondary alcohols containing 8 to 22 carbon atoms are more effective than linear primary alcohols for enhancing the integrity, in contact with water, of bars containing certain anionic detergents.
Thus, according to this invention, there is provided a built, non-soap detergent bar containing 10 to 60% by weight of non-soap anionic detergent active, at least a majority and preferably at least fourfifths of which is selected from the group consisting of linear or branched C8 to C18 alkylbenzene sulphonates, C8 to C18 alkyl sulphates and mixtures thereof, the amount of detergent active selected from said group being at least 10% by weight of the bar; and 5 to 60% by weight of detergency builder; wherein the bar additionally contains from 0.3 to 10% by weight of at least one secondary alcohol or branched-chain primary alcohol containing in either case 8, better 10 up to 24 carbon atoms.
The features of this invention, and also some preferred and optional features, will now be discussed in turn: Detergent active As already mentioned, the composition includes nonsoap detergent active in an amount from 10 to 60wt% of the overall composition. It is envisaged that the amount will generally range from 12 to 40 or 45wt% and a particularly envisaged range is from 15 to 4Owt%. Amounts over 45wt% up to 6Owt% may, however, be used. Preferably the total of all detergent active does not exceed 65 wt%.
Anionic detergent actives required as more than half of the anionic detergent present in bars of the present invention are either or both of: alkylbenzene sulphonates of formula R-C6H4-SO3M and primary alkyl sulphates, also known as primary alcohol sulphates, of formula ROSO3M wherein in each formula R is a linear or branched primary alkyl or alkenyl group containing 8 to 22 carbon atoms, preferably 10 to 18 carbon atoms and M is a cation such that the detergent active is water soluble.
In primary alkyl sulphate R will frequently be linear alkyl of 8 to 22 carbon atoms, preferably of 10 to 16 or 18 carbon atoms. In alkylbenzene sulphonate R may be linear or branched alkyl of 8 to 22 carbon atoms and preferably contains 8 to 16 carbon atoms.
The detergent active may consist solely of primary alkyl sulphate. However, it is envisaged that the detergent active will usually be alkylbenzene sulphonate (either branched or linear) or a mixture of alkylbenzene sulphonate and primary alkyl sulphate in a weight ratio ranging from 3:1 to 1:9, more likely 2:1 to 1:6 or 1:4, yet more preferably a weight ratio ranging from 1:1 to 1:3.
Other detergent actives which may be used in lesser amount include alkane sulphonates, secondary alcohol sulphates, olefin sulphonates, fatty acid ester sulphonates, ethoxylated alcohol sulphates, betaines, amine oxides and fatty acid isethionates. Fatty acyl amides and alkanolamides which are polar nonionic detergents, may also be employed. A suitable amount of these polar nonionic detergents is 3% by weight of the bar composition.
It is possible within the scope of the invention to include soap but it would generally be absent because it inhibits the formation of lather by the non-soap detergent active. Consequently it is preferred that if soap is present at all, the amount of it does not exceed 2% by weight of the bar composition.
Secondary and branched chain alcohols The branched chain or secondary alcohol used in this invention must contain from 8 to 24 carbon atoms.
Preferred is at least 10 or 11 carbon atoms. The number of carbon atoms will generally not exceed 20 and a range from 11 to 18 is preferred.
The amount of such alcohol must be from 0.3 to 10% by weight, Generally it will be adequate to use amounts up to 5 or even up to 3% by weight. Preferred is to use at least 0.5% by weight better at least 1%.
Bars in accordance with this invention may contain secondary or branched alcohol without any significant content of linear primary alcohol.
Alternatively a mixture of alcohols may be used which includes some linear primary alcohol - preferably as a minority of such a mixture.
Branched chain alcohols Branched chain alcohols can be depicted by a schematic formula
where n is at least one and R1 and R2 are alkyl or alkenyl groups, probably differing in length. R1 and R2 may both be linear alkyl or alkenyl, although they can also be branched.
One preferred category of branched chain alcohols is the Guerbet alcohols which have branching at the 2position and so have the schematic formula
where R1 and R2 are both linear or branched alkyl or alkenyl groups, usually both linear alkyl.
These alcohols can be made by the Guerbet reaction which is a high temperature condensation reaction between two alcohol molecules, leading to a 2-alkylalkanol. The reaction can be represented as:
If a mixture of alcohols is used the reaction can take place between different alcohol molecules, thus
as well as taking place between molecules which are the same.
The reaction is brought about by heating in the presence of a catalyst. Various materials can serve as catalyst, notably nickel and lead salts, oxides of copper, lead, zinc chromium, molybdenum, tungsten and manganese, and also compounds of palladium and of silver.
A series of Guerbet alcohols containing from 12 to 24 carbon atoms is'available from M. Michel and Co. Inc. New York. They do not contain any substantial quantity of linear alcohol. Guerbet alcohols are also available from Condea Chemie, Hamburg.
A mixture of alcohols incorporating a high proportion of alcohols with branching at the 2-position can be made by the Oxo process. Such a mixture typically contains branched alcohols in a quantity which is more than four times the quantity of linear alcohols.
Such alcohols are available as the Lial series of alcohols, from Enichem, Augusta, Sicily. For example Lial 125 contains a mixture of alcohols with 12 to 15 carbon atoms. Linear alcohols constitute 40% of the mixture while 60% of the mixture are alcohols with branches at the 2-position.
Lial 111 is C11 alcohol of which 50% is straight chain and 50% is branched at the 2-position.
Lial 123 is a mixture of C1 2 and C13 alcohols, 58% of which are branched.
Acropol 35, available from Exxon at either Harnes, France or Rozenburg, Netherlands is a mixture of C1 3 alcohols and C1 5 alcohols.
Linear C1 3 and C alcohols were found to provide 65% of a sample. The remainder is mostly C1 3 and C15 alcohols branched at the 2-position.
Secondary alcohols These can be depicted by the general formula
where R1 and R2 are linear or branched alkyl or alkenyl groups, probably differing in length.
Such alcohols are supplied under the Trade Mark Softanol by Nippon Shokubai, Osaka, Japan.
It will usually be the case that the amount of anionic detergent active is at least three, and possibly at least four or five times the amount of secondary or branched alcohol.
Detergency builder Bars according to this invention incorporate from 5 to 60% by weight of detergency builder, preferably from 10 to 45%. The detergency builder may be water-soluble builder, water-insoluble builder, or a mixture of the two.
Examples of water-soluble builder components are: water soluble phosphate salts, e.g. sodium and potassium, tripolyphosphate, pyrophosphate and orthophosphate; water soluble carbonates, e.g. sodium carbonate; organic builders, e.g. sodium nitrilotriacetate, sodium tartrate, sodium citrate, trisodium carboxymethyl oxysuccinate, sodium oxydisuccinate, sodium sulphonated long-chain monocarboxylic acids, polyacrylates and oxidised polysaccharides. Significant forms of this invention are bars in which the builder comprises water-soluble phosphate or polyphosphate detergency builder in an amount which is at least 10% by weight of the bar composition.
A water-insoluble detergent builder which may be included in a bar formulation is aluminosilicate ion exchanger, such as natural and synthetic zeolites. This may possibly be used in amounts up to 40% by weight of the bar, e.g. 5 to 40%.
Water-insoluble material Bars according to this invention will usually contain up to 40% by weight of water-insoluble material, notably from 2% or 5% up to 40%.
It is conventional that bars include water-insoluble material, customarily referred to as filler which helps to form the structure of the bar. Clays, notably kaolin and bentonite are conventional for this purpose. If a waterinsoluble detergency builder is present, this will also contribute to the content of water-insoluble material.
Although it is not an essential feature, bars embodying this invention may include a structuring system consisting of a water-insoluble metal compound precipitated during manufacture of the bars. GB Patent 2,099,013 describes the use of aluminium salts and a soluble silicate to form aluminosilicate in situ.
GB 2,234,982A describes the use of further polyvalent metal compounds and siliceous compounds to provide a structuring system. GB 2,235,205A discloses the use of phosphates in the provision of water-insoluble structuring material. These prior disclosures are incorporated herein by reference.
The systems of one or other of these prior disclosures are preferably used in the bars of the present invention and contribute to the content of water-insoluble material.
Other ingredients The bars of this invention may optionally include various other materials, both soluble and insoluble.
Water-soluble salts such as sodium and potassium sulphate may be included as a filler.
The water-soluble alkali metal salts of those sulphur oxo acids which are reducing agents may be included in the composition as bleaches. Preferred is to incorporate from 1 to 15% by weight of such material, better at least 2% or even at least 7.5% by weight. These materials can be used in conjunction with a photobleach such as aluminium phthalocyanine sulphonate.
Other detergent additives include antiredeposition agents such as sodium carboxymethyl cellulose, starches, colouring materials, fluorescers, polyvinyl pyrrolidones, protein hydrolysates and germicides, opacifiers, humectants such as glycerol, polyethylene glycols, perfumes and alternative bleaches such as sodium perborate and potassium monopersulphate. Enzymes may also be included: notably proteases, lipases amylases and cellulases.
Linear fatty alcohols (without ethoxylation) such as coconut alcohol may be incorporated in bars according to this invention if desired. Some fatty alcohol is likely to be included in commercial supplies of primary alkyl sulphate, since alcohol sulphate invariably contains some unsulphated material, and there can also be decomposition to fatty alcohol during bar manufacture. However, there is no necessity to incorporate such linear fatty alcohols in addition to the amount, if any, which is present as an impurity.
Detergent bars according to this invention may be formulated to yield an alkaline liquor when used. This may be done by including sodium carbonate and/or sodium silicate to raise the alkalinity, (typically to a pH in the range 9.8 to 11.4 when determined as below).
However, we have found that it is both possible and advantageous to formulate detergent bars so as to give a reduced alkaline pH when placed in water. Accordingly the composition of bars embodying this invention may be such that the composition generates a pH in the range from 7.0 to 9.8 when mixed with deionised water at a weight ratio of composition: water of 2.5:97.5 and allowed to dissolve as completely as possible at a temperature of 20"C.
In practice the pH of a composition will not vary much with temperature, so that a pH value measured at any temperature in the range from 15"C to 30"C will be adequately accurate.
It is preferred that the pH, measured at 20"C as stated above, lies in a range from 7.5 to 9.6. The pH may well lie above a lower limit of pH 8.0. Alternatively, or in addition, it may lie in a range not exceeding pH 9.3 or even pH 9.2.
Depending on the intended pH other less alkaline salts may be introduced to provide further control of the pH. Thus for instance sodium carbonate may be at least partially replaced with bicarbonate or borax. Phosphate acid builder salts can help to buffer the pH which is developed on mixing with water. Metal salts which are acidic in solution may be present, for example zinc salts in amounts up to 10% by weight.
In use, of course, the proportions of mixing with water are not controlled and deionised water is not used.
Nevertheless the pH which is generated in use will be adequately related to that measured under the stated conditions, since it is largely controlled by the salts in the composition.
To prepare bars according to this invention, it is preferred to use if possible the acid form of the detergent(s) active, neutralising them in a mixer and adding other ingredients such as insoluble filler(s), phosphate builder(s) and finally minor ingredients such as perfume. In the case of alkyl sulphate it is not possible to use the acidic form of the detergent, because it decomposes to the primary alcohol from which it was made.
Therefore alkyl sulphates are added to the mixture in the form of their alkali metal salts.
Mixing can be carried out in a high shear mixer and be followed by conventional extrusion and bar stamping.
The required secondary or branched alcohol may be added at any stage, but preferably after neutralisation.
GB 2,099,013, 2,234,982 and 2,235,205 explain when to add materials which react in situ to form an insoluble structuring system.
Neutralisation is preferably effected by the known procedure of dry neutralisation, in which a carbonate (usually soda ash) is added to the acidic mixture.
Neutralisation in other ways, such as with very concentrated sodium hydroxide solution or a mixture of sodium hydroxide and soda ash, is also possible.
The invention will be further explained and illustrated by means of the following examples, in which all proportions and percentages are by weight unless otherwise stated.
In these examples, bars with the compositions given were manufactured on a conventional plant for the manufacture of NSD bars. This plant consisted of a sigma mixer, mill and vacuum plodder.
All mixing of ingredients took place in the mixer, as did neutralissation of the acid form of the anionic detergent, as indicated above. When the anionic detergent included primary alkyl sulphate, this was added to the mixer in pre-neutralised (i.e. sodium salt) form.
All bars were made with the same dimensions.
The bars were tested for hardness, integrity when wet, and rate of wear.
Hardness was measured using a SUR PNR10 penetrometer, fitted with a needle of 9 cone angle and a 100 g weight.
An initial measurement was made on freshly extruded bars and a "final" measurement was made after 3 days.
Integrity of bars when wet was measured by the following test for mush formation and loss. The test bar is weighed, and then suspended partially immersed in a 400 ml beaker containing 250 ml water of 20C French hardness at 26"C such that a 3 cm length of the bar is immersed in the water. The bar is left in the water for six hours. During this period some of the bar material forms a sediment at the bottom of the beaker whilst some dissolves into solution. The bar is then withdrawn from the beaker and placed on a petri dish and scraped with a knife to remove soft mush clinging to its surface. The remaining bar is dried to constant weight in an oven. The difference in its weight at the end of the experiment and its starting weight is the weight lost on mushing.
It will be appreciated that the above test is a realistic assessment of loss of weight in a typical wash procedure.
Rate of wear is measured as the loss in bar weight during a procedure in which a bar is rubbed 500 times (by machine) on a test cloth wetted with water of 20 French hardness at ambient temperature.
The pH of the bars was tested as mentioned above by mixing bar composition with deionised water in weight ratio 2.5:97.5, allowing to dissolve as completely as possible at 20"C, and then measuring the pH of the solution.
Example 1 Bars were prepared using a mixture of primary alkyl sulphate and alkyl benzene sulphonate as anionic detergent. The bars contained 2% by weight of various alcohols which were: coconut alcohol (used to provide a comparison), which is a mixture of linear primary alcohols mostly of 12 and 14 carbon atoms, a Guerbet alcohol of 12 carbon atoms, available as Michel XO-150-12. It consists of a mixture of alcohols of 12 carbon atoms, branched at the 2-position, a secondary alcohol which was 2-dodecanol.
LIAL 125, a commercial mixture of C12 -C15 alcohols mostly branched at the 2-position. It can be described briefly as containing 20.8% Cm 2, 30.4% Cm 3, 17.7% C15 chain lengths with 60.3% branching. The various alcohols present in this mixture are set out in more detail in Table 1 below.
TABLE 1 LIAL 125 20.8% C12 30.4% C13 30.8% C14 17.7% C15 with 60.3% branching LINEAR SIDE CHAIN MAIN CHAIN % NONE C12 10.5 C11 2-METHYL C11 3.5 C10 2-ETHYL Cic 1.8 C9 2-PROPYL C9 1.9 2-BUTYL C8) 3.1 2-PENTYL C7 } NONE C13 11.2 2-METHYL C12 5.0 2-ETHYL C11 2.8 2-PROPYL C10 3.3 2-BUTYL C9 3.8 2-PENTYL C8 4.3 NONE C14 12.2 2-METHYL C13 4,4 2-ETHYL C12 2.5 2-PROPYL C11 2.8 2-BUTYL C10 3.4 2-PENTYL C9 } 5.5 2-HEXYL C8 } NONE C15 5.8 2-METHYL C14 2.3 2-ETHYL C13 1.3 2-PROPYL C12 1.6 2-BUTYL C11 2.1 2-PENTYL C10 2.4 2-HEXYL C9 2.2 Formulations of the bars and their observed properties are given in the following Table 2.
The initials PAS denote sodium salt of coconut alcohol sulphate.
The initials ABS denote sodium alkyl benzene sulphonate having approximately twelve carbon atoms in its alkyl chain.
STP is sodium tripolyphosphate.
TABLE 2 INGREDIENTS % BY WEIGHT COCONUT ALCOHOL 2 0 0 0 LIAL 125 0 2 0 0 C12 GUERBET ALCOHOL O 0 2 0 SECONDARY ALCOHOL O 0 0 2 PAS 18 18 18 18 ABS 12 12 12 12 SULPHURIC ACID 3 3 3 3 SODA ASH IN EXCESS O 0 0 0 OF AMOUNT FOR NEUTRALISATION SILICA 2 2 2 2 ALKALINE SILICATE 6 6 6 6 (48%) ALUMINIUM SULPHATE 7.4 7.4 7.4 7.4 HYDRATE STP 15 15 15 15 KAOLIN 6 6 6 6 SODIUM SULPHATE 6.4 6.4 6.4 6.4 SODIUM SULPHITE 8 8 8 8
MINOR INGREDIENTS < ---BALANCE TO 100%---- > AND WATER PROPERTIES TOTAL WATER:: THEORETICAL 13.4 13.4 13.4 13.4 MEASURED 10.9 10.1 11.9 11.3 pH 9.4 9.4 9.3 9.3 PENETROMETER (mm) INITIAL 6.4 7.0 7.0 11.6 FINAL 0.5 0.5 0.6 0.8 RATE OF WEAR (g) 6.0 5.6 5.6 5.2 MUSH LOSS (g) 13.2 9.7 7.2 10.5 As can be seen from Table 2 above the addition of the secondary or branched alcohols gave an improvement in mush formation and loss better than with 2% coconut fatty alcohol without serious detriment to the values for final hardness and rate of wear.
Example 2 Example 1 was repeated using different alcohols.
Two formulations used a C1 6 Guerbet alcohol (Michel XO-150-16) in different amounts, and two formulations used mixtures of C1 2 Guerbet alcohol and C1 6 Guerbet alcohol.
The formulations and results are set out in Table 3 below. Again there was an advantageous reduction in mush formation and loss, better than achieved with coconut alcohol.
TABLE 3 INGREDIENTS % BY WEIGHT COCONUT ALCOHOL 2 0 0 0 C12 GUERBET ALCOHOL 0 1.75 0.25 0 C,, GUERBET ALCOHOL 0 0.25 1.75 1 PAS 18 18 18 18 ABS 12 12 12 12 SULPHURIC ACID 3 3 3 3 SODA ASH IN EXCESS O 0 0 0 OF AMOUNT FOR NEUTRALISATION SILICA 2 2 2 2 ALKALINE SILICATE 6 6 6 6 (48%) ALUMINIUM SULPHATE 7.4 7.4 7.4 7.4 HYDRATE STP 15 15 15 15 KAOLIN 6 6 6 6 SODIUM SULPHATE 6.4 6.4 6.4 6.4 SODIUM SULPHITE 8 8 8 8
MINOR INGREDIENTS < ---BALANCE TO 100%---- > AND WATER PROPERTIES TOTAL WATER:: THEORETICAL 13.4 13.4 13.4 13.4 MEASURED 10.9 11.9 10.9 9.8 pH 9.4 9.3 9.3 9.4 PENETROMETER (mm) INITIAL 6.4 7.0 8.5 5.8 FINAL 0.5 0.6 0.7 0.7 RATE OF WEAR (g) 6.0 5.6 5.7 6.5 MUSH LOSS (g) 13.2 7.2 8.2 11.6 Example 3 Example 1 was repeated using a different formulation in which phosphate contributes to bar structuring.
Several concentrations of LIAL 125 were used. The formulations and results are set out in Table 4 below.
The improvement given by 2% of LIAL 125 was improved by increasing the quantity to 3% and 4%.
TABLE 4 INGREDIENTS % BY WEIGHT COCONUT ALCOHOL 2 0 0 0 0 LIAL 125 0 2 3 4 0 Cl2 GUERBET ALCOHOL O 0 0 0 2 PAS 18 18 18 18 18 ABS 12 12 12 12 12 SULPHURIC ACID 3 3 3 3 3 SODA ASH IN EXCESS O 0 0 0 0 OF AMOUNT FOR NEUTRALISATION SILICA 2 2 2 2 2 ALUMINIUM SULPHATE 7.4 7.4 7.4 7.4 7.4 HYDRATE STP 15 15 15 15 15 KAOLIN 6 6 6 6 6 SODIUM SULPHATE 10.9 10.9 9.9 8.9 10.9 SODIUM SULPHITE 8 8 8 8 8
MINOR INGREDIENTS < ---BALANCE TO 100%---- > AND WATER PROPERTIES TOTAL WATER:: THEORETICAL 9.2 9.2 9.2 9.2 9.2 MEASURED 8.2 8.2 8.9 10.2 8.9 pH 9.4 9.4 9.3 9.5 9.6 PENETROMETER (mm) INITIAL 4.8 4.8 4.4 6.5 4.9 FINAL 0.6 0.6 0.6 0.7 0.7 RATE OF WEAR (g) 5.8 5.9 5.8 5.5 5.7 MUSH LOSS (g) 16.0 15.0 11.0 7.5 9.3 Example 4 The procedure of Example 1 was repeated using formulations of higher pH, with either coconut alcohol (comparative) or C1 2 Guerbet alcohol. Formulations and results are set out in Table 5 below.
TABLE 5 INGREDIENTS % BY WEIGHT COCONUT ALCOHOL 2 0 C1 2 GUERBET ALCOHOL 0 2 PAS 18 18 ABS 12 12 SULPHURIC ACID 1.8 1.8 SODA ASH IN EXCESS 13.4 13.4 OF AMOUNT FOR NEUTRALISATION SILICA 2 2 ALKALINE SILICATE 4 4 (48%) ALUMINIUM SULPHATE 5.3 5.3 HYDRATE STP 9 9 SODIUM PYROPHOSPHATE 4 4 CALCITE 11 11 KAOLIN 6 6 BENTONITE 2 2
MINOR INGREDIENTS < ---BALANCE TO 100%---- > AND WATER PROPERTIES TOTAL WATER: THEORETICAL 7.8 7.8 MEASURED 7.2 7.3 pH 10.4 10.4 PENETROMETER (mm) INITIAL 6.0 7.7 FINAL 0.6 0.5 RATE OF WEAR (g) 5.0 4.8 MUSH LOSS (g) 11.2 9.8 Example 5 The procedure of Example 1 was repeated using formulations containing linear alkyl benzene sulphonate as the only anionic detergent active) Formulations and results are set out in Table 6 below.
TABLE 6 INGREDIENTS % BY WEIGHT COCONUT ALCOHOL 2 0 0 LIAL 125 0 2 0 C12 GUERBET ALCOHOL O 0 2 ABS 22 22 22 SODA ASH IN EXCESS 0.5 0.5 0.5 OF AMOUNT FOR NEUTRALISATION ALKALINE SILICATE 7 7 7 (48%) ALUMINIUM SULPHATE 8 8 8 STP 12.5 12.5 12.5 CALCITE 7.6 7.6 7.6 KAOLIN 22.8 22.8 22.8 SODIUM SULPHITE 7.5 7.5 7.5
MINOR INGREDIENTS < ---BALANCE TO 100%---- > AND WATER PROPERTIES TOTAL WATER: THEORETICAL 12.5 12.5 12.5 MEASURED 9.9 10.3 8.2 pH 9.5 9.5 9.6 PENETROMETER (mm) INITIAL 6.9 7.2 5.5 FINAL 2.0 1.9 1.2 RATE OF WEAR (g) 6.6 6.3 6.0 MUSH LOSS (g) 9.8 8.9 9.4 Example 6 The procedure of Example 1 was repeated using formulations containing coconut alkyl sulphate as the only anionic detergent active.
Formulations and results are set out in Table 7 below.
TABLE 7 INGREDIENTS t BY WEIGHT LIAL 2 0 C12 GUERBET ALCOHOL 0 2 UREA 1 1 MONOETHANOLAMINE 1 1 PAS 30 30 SODA ASH 5.3 5.3 ALKALINE SILICATE 6.1 6.1 (48%) ALUMINIUM SULPHATE 7.4 7.4 HYDRATE SODIUM PYROPHOSPHATE 17.5 17.5 CALCITE 19.7 19.7
MINOR INGREDIENTS < ---BALANCE TO 100%---- > AND WATER PROPERTIES TOTAL WATER: THEORETICAL 12.0 12.0 MEASURED 11.5 11.5 pH 10 10 PENETROMETER (mm) INITIAL 13.8 11.3 FINAL 0.3 0.4 RATE OF WEAR (g) 6.3 6,2 MUSH LOSS (g) 13.6 12.9 Example 7 Bars were made with two formulations containing bentonite. The second of the formulations was in accordance with this invention.
The formulations and results are set out in the following Table 8.
TABLE 8 INGREDIENTS % BY WEIGHT COCONUT ALCOHOL 2 0 C12 GUERBET ALCOHOL 0 2 PAS 18 18 ABS 12 12 SULPHURIC ACID 3 3 SODA ASH IN EXCESS O 0 OF AMOUNT FOR NEUTRALISATION SILICA 2 2 ALKALINE SILICATE 6 6 (48%) ALUMINIUM SULPHATE 7.4 7.4 HYDRATE STP 15 15 KAOLIN 10.4 10.4 BENTONITE 2 2 SODIUM SULPHITE 8 8
MINOR INGREDIENTS < ---BALANCE TO 100%---- > AND WATER PROPERTIES TOTAL WATER: THEORETICAL 13.4 13.4 MEASURED 11.7 10.9 pH 9.3 9.3 PENETROMETER (mm) INITIAL 7.5 5.8 FINAL 0.3 0.6 RATE OF WEAR (g) 5.4 5.4 MUSH LOSS (g) 12.4 8.6

Claims (12)

  1. CLAIMS: 1. A built, non-soap detergent bar containing
    10 to 60% by weight of non-soap anionic detergent active, at least a majority of which is selected from the group consisting of linear or branched Ca to C2 2 alkylbenzene sulphonates, Ca to C2 2 alkyl sulphates and mixtures thereof, the amount of detergent active selected from said group being at least 10% by weight of the bar; and
    5 to 60% by weight of detergency builder; wherein the bar additionally contains from 0.3 to 10% by weight of at least one secondary alcohol or branched-chain primary alcohol containing in either case 8 to 24 carbon atoms.
  2. 2. A bar according to claim 1 wherein the amount of said secondary or branched-chain alcohol is in the range from 0.3 to 5% by weight.
  3. 3. A bar according to claim 1 wherein said alcohol is a primary alcohol of formula
    wherein R1 and R2 are alkyl or alkenyl groups containing in total 8 to 18 carbon atoms.
  4. 4. A bar according to claim 1, claim 2 or claim 3 wherein a majority of the anionic detergent active is alkylbenzene sulphonate.
  5. 5. A bar according to claim 1, claim 2 or claim 3 wherein a majority of the anionic detergent active is primary alcohol sulphate.
  6. 6. A bar according to claim 1, claim 2 or claim 3 wherein a majority of the anionic detergent active is a mixture of alkylbenzene sulphonate and primary alcohol sulphate in a weight ratio lying in a range from 3:1 to 1:9.
  7. 7. A bar according to any one of the preceding claims wherein the detergency builder comprises water-soluble detergency builder in an amount which is at least 3% by weight of the bar.
  8. 8. A bar according to claim 7 wherein the watersoluble detergency builder comprises alkali metal orthophosphate, pyrophosphate or tripolyphosphate in an amount which is from 3% to 30% by weight of the bar.
  9. 9. A bar according to any one of the preceding claims wherein the bar comprises 2% to 40% by weight of waterinsoluble material.
  10. 10. A bar according to any one of the preceding claims which generates a pH in the range from 7.0 to 9.8 when mixed with deionised water at a weight ratio of bar composition: water of 2.5:97.5 and allowed to dissolve as completely as possible at a temperature of 20"C.
  11. 11. A bar according to claim 10 wherein the pH lies in a range from 7.5 to 9.6.
  12. 12. A bar according to any one of claims 1 to 9 which generates a pH in the range from 9.8 to 11 when mixed with deionised water at a weight ratio of bar composition: water of 2.5:97.5 and allowed to dissolve as completely as possible at a temperature of 20"C.
GB9310155A 1993-05-17 1993-05-17 Detergent composition Withdrawn GB2278124A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB9310155A GB2278124A (en) 1993-05-17 1993-05-17 Detergent composition
IN216BO1994 IN182011B (en) 1993-05-17 1994-05-16
MYPI9401221 MY118466A (en) 1993-05-17 1994-05-16 Detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB9310155A GB2278124A (en) 1993-05-17 1993-05-17 Detergent composition

Publications (2)

Publication Number Publication Date
GB9310155D0 GB9310155D0 (en) 1993-06-30
GB2278124A true GB2278124A (en) 1994-11-23

Family

ID=10735630

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9310155A Withdrawn GB2278124A (en) 1993-05-17 1993-05-17 Detergent composition

Country Status (3)

Country Link
GB (1) GB2278124A (en)
IN (1) IN182011B (en)
MY (1) MY118466A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995027036A1 (en) * 1994-03-30 1995-10-12 The Procter & Gamble Company Laundry detergent bars containing fabric softening clay and cellulase enzyme
WO1995027038A1 (en) * 1994-03-30 1995-10-12 The Procter & Gamble Company Laundry detergent bars with improved whitening and dye transfer inhibition
GB2296920A (en) * 1995-01-16 1996-07-17 Unilever Plc Detergent bars
WO1998012294A1 (en) * 1996-09-20 1998-03-26 Unilever Plc Antimicrobial cleaning compositions
WO2017079960A1 (en) * 2015-11-13 2017-05-18 The Procter & Gamble Company Cleaning compositions containing branched alkyl sulfate surfactants and linear alkyl sulfate surfactants
US10266791B2 (en) 2015-11-13 2019-04-23 The Procter & Gamble Company Detergent compositions
US10647944B2 (en) 2015-11-13 2020-05-12 The Procter & Gamble Company Cleaning compositions containing branched alkyl sulfate surfactant with little or no alkoxylated alkyl sulfate
US10876072B2 (en) 2015-11-13 2020-12-29 The Procter & Gamble Company Cleaning compositions containing a branched alkyl sulfate surfactant and a short-chain nonionic surfactant

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2145109A (en) * 1983-08-17 1985-03-20 Colgate Palmolive Co Sodium higher fatty alkyl sulphate detergent laundry bars
EP0281028A2 (en) * 1987-03-05 1988-09-07 Henkel Kommanditgesellschaft auf Aktien Shaped detergent
US5089174A (en) * 1989-01-19 1992-02-18 The Procter & Gamble Company Laundry detergent bars free of C12 -C18 fatty acids and containing an alkylbenzene sulfonate, an alkyl sulfonate and a fatty alcohol

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2145109A (en) * 1983-08-17 1985-03-20 Colgate Palmolive Co Sodium higher fatty alkyl sulphate detergent laundry bars
EP0281028A2 (en) * 1987-03-05 1988-09-07 Henkel Kommanditgesellschaft auf Aktien Shaped detergent
US5089174A (en) * 1989-01-19 1992-02-18 The Procter & Gamble Company Laundry detergent bars free of C12 -C18 fatty acids and containing an alkylbenzene sulfonate, an alkyl sulfonate and a fatty alcohol

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995027036A1 (en) * 1994-03-30 1995-10-12 The Procter & Gamble Company Laundry detergent bars containing fabric softening clay and cellulase enzyme
WO1995027038A1 (en) * 1994-03-30 1995-10-12 The Procter & Gamble Company Laundry detergent bars with improved whitening and dye transfer inhibition
GB2296920A (en) * 1995-01-16 1996-07-17 Unilever Plc Detergent bars
WO1998012294A1 (en) * 1996-09-20 1998-03-26 Unilever Plc Antimicrobial cleaning compositions
WO2017079960A1 (en) * 2015-11-13 2017-05-18 The Procter & Gamble Company Cleaning compositions containing branched alkyl sulfate surfactants and linear alkyl sulfate surfactants
US10266791B2 (en) 2015-11-13 2019-04-23 The Procter & Gamble Company Detergent compositions
US10647944B2 (en) 2015-11-13 2020-05-12 The Procter & Gamble Company Cleaning compositions containing branched alkyl sulfate surfactant with little or no alkoxylated alkyl sulfate
EP3666868A1 (en) * 2015-11-13 2020-06-17 The Procter & Gamble Company Cleaning compositions containing branched alkyl sulfate surfactants and linear alkyl sulfate surfactants
US10876072B2 (en) 2015-11-13 2020-12-29 The Procter & Gamble Company Cleaning compositions containing a branched alkyl sulfate surfactant and a short-chain nonionic surfactant
EP4276162A3 (en) * 2015-11-13 2024-01-31 The Procter & Gamble Company Cleaning compositions containing branched alkyl sulfate surfactants and linear alkyl sulfate surfactants

Also Published As

Publication number Publication date
GB9310155D0 (en) 1993-06-30
IN182011B (en) 1998-12-05
MY118466A (en) 2004-11-30

Similar Documents

Publication Publication Date Title
CA2034666C (en) Detergent composition
CA2182158C (en) Detergents and cleaners containing iminodisuccinates
US3741911A (en) Phosphate-free detergent composition
EP0342917B1 (en) Detergent composition
PL204555B1 (en) Detergent composition for washing and the method of washing textile fabrics
DE4402051A1 (en) Builder for detergents or cleaners
JPH0559394A (en) Detergent composition
US4206070A (en) Detergent compositions
JPH0639593B2 (en) Detergent composition containing alkylbenzene sulphonate and alcohol ethoxy sulphate surfactant system
GB2278125A (en) Detergent composition
GB2278124A (en) Detergent composition
CA1323818C (en) Detergent composition
US4547306A (en) Fabric detergent compositions containing acylcyanamides
BR0112852B1 (en) laundry particulate detergent composition; and, color particulate composition for use as a color splash composition in a laundry detergent composition.
GB1560073A (en) Detergent compositions and the production thereof
BR0313827B1 (en) Washing detergent composition
CZ312997A3 (en) Detergent and process of wetting clothes
US3832309A (en) Detergent formulations
CA1191068A (en) Detergent additives and detergent compositions containing them
CA1314189C (en) Detergent compositions
GB2291067A (en) Detergent Composition
GB2276630A (en) Non-soap detergent bar
JPS6021640B2 (en) liquid detergent composition
AU598489B2 (en) Detergent composition of improved oily soil removing capability
KR960007394B1 (en) Detergent compositions

Legal Events

Date Code Title Description
WAP Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1)