GB2224035A - Detergent composition - Google Patents
Detergent composition Download PDFInfo
- Publication number
- GB2224035A GB2224035A GB8823009A GB8823009A GB2224035A GB 2224035 A GB2224035 A GB 2224035A GB 8823009 A GB8823009 A GB 8823009A GB 8823009 A GB8823009 A GB 8823009A GB 2224035 A GB2224035 A GB 2224035A
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- GB
- United Kingdom
- Prior art keywords
- clay
- detergent
- sodium
- fabric
- clays
- 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.)
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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
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
- C11D3/126—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in solid compositions
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
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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)
Abstract
A detergent composition for washing and softening fabrics comprising at least one detergent active material and, as a fabric softening agent, a smectite clay mineral which is a 2:1 layer phyllosilicate possessing a lattice charge deficiency in the range of 0.2 to 0.4g equivalents per half unit cell.
Description
DETERGENT COMPOSITIONS
This invention relates to detergent compositions, in particular to detergent compositions for washing fabrics and providing said fabrics with a softening benefit.
It is common practice to wash fabrics in detergent compositions which contain a detergent active material for removing soil from the fabrics. With some fabrics, especially of natural origin, repeated washing can lead to fabric harshness, giving the fabrics an unpleasant feel.
For some years fabric conditioning products have been available, intended inter alia for alleviating this fabric harshness by softening the fabrics in a post-washing step, eg. in the rinse step of a fabric laundering process.
There has been a desire to provide a single detergent composition which would be capable of both washing and softening the fabrics to overcome the inconvenience of using separate products. According to British Patent
Specification GB1400898 (Procter & Gamble) a possible solution to this problem is to include in the detergent composition a three-layer smectite clay containing material having a cation exchange capacity of at least 50 meq/lOOg, together with an anionic or similar detergent active material.
While some success has been obtained with the use of such clay materials, softening performance still does not generally match that obtained by the use of separate products and there is therefore still some scope for further improving performance.
We have now discovered a specific class of clay materials which are capable of generating softening benefits better than those obtained by the use of the clays disclosed in the above mentioned art.
Thus according to the invention there is provided a detergent composition for washing and softening fabrics comprising at least one detergent active material and, as a fabric softening agent, a smectite clay mineral which is a 2:1 layer phyllosilicate possessing a lattice charge deficiency in the range of 0.2 to 0.4g equivs. per half unit cell.
The smectite clays taught in the art are 2:1 layer phyllosilicates characterised by possessing a lattice charge deficiency in the range of 0.2 to 0.6g equivs. per half unit cell, which results in an exchange capacity of say 60 to 150 meq per 100g of mineral. We have now found that certain clays give better softening performance than others and that the common feature of these materials is that they contain smectite minerals in which the lattice charge deficiency is at the lower end of the range, ie.
from 0.2 to 0.4g equivs. per half unit cell.
In general, clays which are useful in the present invention fall into the formula: (Si, Al yAly)(A12 a bM aN b) 10(OH)2XIy+b in which MIII is a trivalent metal ion most commonly being selected from iron, chromium, manganese and mixtures thereof, N11 is a divalent metal ion most commonly being selected from magnesium, iron and mixtures thereof, y is zero or a positive number less than 4, a and b are positive numbers less than 2 such that y + b is from 0.2 to 0.4 and XI is a balancing exchangeable cation which can be a univalent inorganic or organic ion or the equivalent amount of a divalent ion, X being most commonly selected from Na, K, Ca, Mg and mixtures thereof.
Such clays are commercially available but have not previously been proposed for use in detergent compositions. Clays that have been proposed include those available under the trade name GELWHITE from Texas, USA and LAVIOSA AGB from Italy but such clays have been found to have a lattice deficiency (y + b) of about 0.54 and in the range 0.46 to 0.55 respectively. Clays useful in the present invention have been found in Wyoming USA, but not all Wyoming clays are suitable. Thus British patent
GB1518529 (Procter & Gamble/Baskerville) discloses a
Wyoming bentonite VOLCLAY BC, which has a very high ion exchange capacity (ie. has a high lattice deficiency) and
United States patent US4582615 (Ramachandran) discloses the use of General Purpose Bentonite from American Colloid
Company also believed to be a Wyoming bentonite.From the analytical data published in US4582615, the best estimate of structure which can be derived leads one to believe that its lattice deficiency is about 0.42.
Clays useful in the present invention include the following:
VOLCLAY SPV USA Fe Fe/Mg 0.01 0.06 0.37
SURREY NO.1
EARTH UK Fe Mg 0 0.41 0.32
ENVIRONETICS Argentina Fe Mg 0 0.12 0.33
CULVIN South
Africa Fe Mg 0.11 0.23 0.28
SAN FRAN Argentina Fe Fe/Mg 0.07 0.15 0.21
BERKBOND 1 UK Fe Mg 0.04 0.58 0.31
STEETLEY
WYOMING USA Fe Mg 0 0.28 0.32
These clays are naturally of both sodium and calcium types (XI = Na or F Ca), and we have found that the nature of the substituent XI is irrelevant to softening performance from a detergent composition.
The following clays are not however useful in the present invention:
Trade Name Origin M N y a b
MDO 77/84
ECC (ASB) ) Morocco Fe Mg 0.26 0.12 0.23
UBM Brazil Fe Mg 0.20 0.06 0.38
CSM (high CEC Greece Fe Mg 0.05 0.08 0.42
Prassa)
STEETLEY Turkey Fe Mg 0.01 0.06 0.60
LAPORTE Spain Fe Mg 0.14 0.08 0.44
GELWHITE Texas USA Fe Mg 0.17 0.05 0.37
WILLEMSE S. Africa Fe Mg 0.33 0.40 0.28
The reason for the improved softening benefits obtained with the selected clays is not fully understood.
While not wishing to be bound by theory one may suppose that differences in lattice charge affect the strength of repulsion forces between the clay and the fabric enabling a higher level of clay to be maintained on the fabric surface even over multiple washes.
The compositions according to the invention may take various physical forms such as powders, liquids, pastes or bars and may contain a variety of additional ingredients.
An essential ingredient is a detergent active material. This may be selected from anionic, nonionic, amphoteric, zwitterionic and cationic materials, with a special preference for synthetic anionic surfactants, with or without nonionic surfactants.
Particularly preferred are mixtures of anionic and nonionic detergent active materials such as a mixture of an alkalimetal salt of an alkyl benzene sulphonate together with an alkoxylated alcohol. The level of detergent active material or materials in the composition may be from 2% to 50%, most preferably from 5% to 30% by weight.
The preferred detergent compounds which can be used are synthetic anionic and nonionic compounds. The former are usually water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.Examples of suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C8-C18) alcohols produced for example from tallow or coconut oil, sodium and potassium linear or branched alkyl (Cg-C20) benzene sulphonates, particularly sodium linear secondary alkyl (C10-Cl5) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or conconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C8-C18) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acid amides of methyl taurine; alkane monosulphonates such as those derived by reacting alpha-olefins (C8-C20) with sodium bisulphite and those derived from reacting'paraffins with SO2 and C12 and then hydrolysing with a base to produce a random sulphonate; olefin sulphonates, which term is used to describe the material made by reacting olefins, particularly C10-C20 alpha-olefins, with S03 and then neutralising and hydrolysing the reaction product; alpha-sulphocarboxylates containing from say 6 to 20 carbon atoms, including not only the salts of alpha-sulphonated fatty acids but also their esters made from alcohols containing from 1 to about 14 carbon atoms and fatty amide sulphonates. The preferred anionic detergent compounds are sodium (C11-C15) alkyl benzene sulphonates and sodium (C16-Cl8) alkyl sulphates.
Suitable nonionic detergent compounds which may be used include in particular the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
Specific nonionic detergent compounds are alkyl (C6-C22) phenols-ethylene oxide condensates, generally up to 25 EO, ie. up to 25 units of ethylene oxide per molecule, the condensation products of aliphatic (C8-C18) primary or secondary linear or branched alcohols with ethylene oxide, generally up to 40 EO, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine. Other so-called nonionic detergent compounds include long chain tertiary amine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
Mixtures of detergent compounds, for example mixed anionic or mixed anionic and nonionic compounds may be used in the detergent compositions, particularly in the latter case to provide controlled low sudsing properties.
This is beneficial for compositions intended for use in suds-intolerant automatic washing machines.
Amounts of amphoteric or zwitterionic detergent compounds can also be used in the compositions of the invention but this is not normally desired due to their relatively high cost. If any amphoteric or zwitterionic detergent compounds are used it is generally in small amounts in compositions based on the much more commonly used synthetic anionic and/or nonionic detergent compounds.
A detergency builder may also be present. This may be any material capable of reducing the level of free calcium ions in the wash liquor and will preferably provide the composition with other beneficial properties such as the generation of an alkaline pH, the suspension of soil removed from the fabric and the suspension of the fabric softening clay material. The level of the detergency builder may be from 10% to 70% by weight, most preferably from 25% to 50% by weight.
Examples of detergency builders include precipitating builders such as the alkali metal carbonates (with or without seed crystals such as calcite), bicarbonates, ortho phosphates, pyrophosphates and mixtures thereof sequestering builders such as the alkali metal tripolyphosphates or nitrilotriacetates, or ion-exchange builders such as the amorphous alkalimetal aluminosilicates or the zeolites.
The clay material can be added in various physical forms. It may, for example, be spray-dried with other components of the formulation or it may be added separately. In the latter case the clay may be ground to a suitable size, say 150 to 2000 microns, or may be in the form of granulated fine particles optionally containing a binder such as an inorganic salt or a surfactant.
Especially suitable binders are sodium silicate and nonionic detergent active materials. When dry mixed clays are utilised any poor colour (often due to trace amounts of certain transition metal ions in the structure) may be disguised by granulating or coating with a white or more acceptably coloured pigment material. Particularly useful coating materials include ultramarine blue, zeolite, calcite, white clay, talc and titanium dioxide. The use of a binding agent in this process is helpful, such as a 30% aqueous solution of a maleic acid/acrylic acid copolymer (eg. Sokalan CP5 ex BASF).
The level of the fabric softening clay material in the composition should be sufficient to provide a softening benefit, such as from 1.5% to 35% by weight, most preferably from 4% to 15% by weight, calculated on the basis of the clay mineral per se.
In addition to the detergent active material, the detergency builder and the clay containing material, the compositions according to the invention optionally contain other ingredients.
Apart from the components already mentioned, a detergent composition of the invention can contain any of the conventional additives in the amounts in which such additives are normally employed in fabric washing detergent compositions. Examples of these additives include the lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids, lather depressants, oxygen-releasing bleaching agents such as sodium perborate and sodium percarbonate, peracid bleach precursors, chlorine-releasing bleaching agents such as triclorisocyanuric acid, inorganic salts such as sodium sulphate, other fillers such as kaolin, and, usually present in very minor amounts, fluorescent agents, perfumes, other enzymes such as proteases and amylases, germicides and colourants.
The invention will now be described in more detail with reference to the following non-limiting examples.
EXAMPLE 1
A detergent composition was prepared having the following formulation:
Ingredient Parts by weight
Alkyl benzene sulphonate 9.0
Alcohol ethoxylate (7EO) 1.0
Alcohol ethoxylate (3EO) 3.0
Sodium tripolyphosphate 21.5
Sodium silicate 5.5
Burkeite 9.0
Water and miscellaneous 12.7
61.7
Washing experiments were carried out by adding 3.085 g/l of this composition to water in a laboratory scale (Tergotometer - Trade Mark) apparatus together with 0.5g/l of clay or no clay as detailed below.
Cotton fabric test pieces were washed, rinsed and dried for six cycles. In the first three cycles the clay was included, in the next two it was omitted and in the final cycle it was included again. After each cycle the amount of clay retained by the fabric was determined using an ashing technique.
Two different clays were used. Clay S was SURREY NO.
1 EARTH and Clay M was MDO 77/84, details of which are given above.
The results obtained were as follows (% clay on fabric):
Cycle Clay S Clay M
1 0.32 0.29
2 0.55 0.45
3 0.66 0.44
4 0.56 0.32
5 0.56 0.25
6 0.67 0.36
It is clear from these results that deposition is greater with Clay S, an apparent stable equilibrium being achieved at approximately 0.56% on the fabric and with an additional reversibly attached level of approximately 0.10%. With Clay M no stable equilibruim resistant to removal is reached.
The softness of the treated fabrics after 6 cycles were compared with one another and with the untreated fabrics with the following results:
Comparison % Preference
Clay S v Clay M 69:31
Clay S v Untreated 100:0
Clay M v Untreated 100:0
While both clays provide a benefit which is preferred over no treatment, Clay S shows a clear preference over
Clay M.
EXAMPLE 2
In these examples a commercially available fabric washing composition was used, having the following approximate composition:
Ingredient % by weight
Alkyl benzene sulphonate 16.0
Sodium tripolyphosphate 11.0
Sodium silicate 9.0
Sodium sulphate 16.5
Sodium carbonate 20.0
Kaolin 14.0
Water and minor ingredients balance
A fabric load comprising a mixture of cotton and polycotton fabrics was washed in water having a hardness of 60FH (6 x 10 molar free calcium ions) using the above composition at a dosage level of 2.5 g/l. The liquor to cloth ratio was 10:1 by weight. The fabrics were soaked for 30 minutes followed by a hand wash and two rinses.
In Examples 2 and 2B, the kaolin was replaced by the same amount of, respectively, VOLCLAY SPV (lattice deficiency 0.37) and UBM (lattice deficiency 0.58) and in
Example 2C the above composition was used as such.
After washing, cotton pieces from the wash load were compared for softness against standards, and given a panel score on a scale ranging from 2 (soft) to 14 (very harsh).
The results were:
Example No. Clay Panel score
2 VOLCLAY 10.3
2B UBM 12.6
2C - 12.3
95% CL to.5 These results shows that both the unmodified product and the product containing the UBM clay gave relatively harsh results whereas the product containing VOLCLAY clay gave significantly superior results.
EXAMPLE 3
Example 2 was repeated with the following differences. The product used had the following composition:
Ingredient % by weight
Alkyl benzene sulphonate 28.0
Sodium tripolyphosphate 25.0
Sodium silicate 7.0
Sodium sulphate 22.5
Sodium carbonate 10.0
Water and minor ingredients balance
Wash conditions were the same as in Example 2 except that the water hardness was 200FH and the product dosage was 7.0g/l.
The clays were used to replace 14% of the sodium sulphate in the composition. In Examples 3 and 3A, the clay used was, respectively, VOLCLAY SPV and CULVIN (lattice deficiency 0.39) in comparative Example 3B the clay was ECC/ASB (lattice deficiency 0.49) and in Example 3C the above composition was used as such.
The results were:
Example No. Clay Panel score 3 VOLCLAY 8.2 3A CULVIN 8.2 3B EEC 10.4 3C - 10.4 95% CL to.5 These results again show that the compositions according to the invention (Examples 3 and 3A) provide a significant benefit over compositions containing alternative clays or over no treatment.
Claims (2)
1. A detergent composition for washing and softening fabrics comprising at least one detergent active material and, as a fabric softening agent, a smectite clay mineral which is a 2:1 layer phyllosilicate posessing a lattice charge deficiency in the range of 0.2 to 0.4g equivs. per half unit cell.
2. A composition according to Claim 1, wherein the smectite clay mineral falls into the formula:
(Si4 yAly)(Al2-a-b MIIIaNIIb)(OH)2XIy+b in which MIII is a trivalent metal ion,
NII is a divalent metal ion,
XI is a balancing exchangeable cation, y is O or a positive number less than 4, and a and b are positive numbers less than 2 such that y+b is from 0.2 to 0.4.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8823009A GB2224035A (en) | 1988-09-30 | 1988-09-30 | Detergent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8823009A GB2224035A (en) | 1988-09-30 | 1988-09-30 | Detergent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
GB8823009D0 GB8823009D0 (en) | 1988-11-09 |
GB2224035A true GB2224035A (en) | 1990-04-25 |
Family
ID=10644536
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8823009A Withdrawn GB2224035A (en) | 1988-09-30 | 1988-09-30 | Detergent composition |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2224035A (en) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1519605A (en) * | 1974-11-18 | 1978-08-02 | Procter & Gamble | Detergent-compatible fabric softening and antistatic compositions |
EP0023367A1 (en) * | 1979-07-05 | 1981-02-04 | THE PROCTER & GAMBLE COMPANY | Detergent composition having textile softening property |
EP0026528A1 (en) * | 1979-09-29 | 1981-04-08 | THE PROCTER & GAMBLE COMPANY | Detergent compositions |
EP0011340B1 (en) * | 1978-11-20 | 1982-11-24 | THE PROCTER & GAMBLE COMPANY | Detergent composition having textile softening properties |
GB2201172A (en) * | 1987-02-20 | 1988-08-24 | Colgate Palmolive Co | No phosphate fabric softening and detergent composition |
EP0297673A2 (en) * | 1987-06-30 | 1989-01-04 | The Procter & Gamble Company | Detergent/softening compositions containing hectorite clays |
-
1988
- 1988-09-30 GB GB8823009A patent/GB2224035A/en not_active Withdrawn
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1519605A (en) * | 1974-11-18 | 1978-08-02 | Procter & Gamble | Detergent-compatible fabric softening and antistatic compositions |
EP0011340B1 (en) * | 1978-11-20 | 1982-11-24 | THE PROCTER & GAMBLE COMPANY | Detergent composition having textile softening properties |
EP0023367A1 (en) * | 1979-07-05 | 1981-02-04 | THE PROCTER & GAMBLE COMPANY | Detergent composition having textile softening property |
EP0026528A1 (en) * | 1979-09-29 | 1981-04-08 | THE PROCTER & GAMBLE COMPANY | Detergent compositions |
GB2201172A (en) * | 1987-02-20 | 1988-08-24 | Colgate Palmolive Co | No phosphate fabric softening and detergent composition |
EP0297673A2 (en) * | 1987-06-30 | 1989-01-04 | The Procter & Gamble Company | Detergent/softening compositions containing hectorite clays |
Also Published As
Publication number | Publication date |
---|---|
GB8823009D0 (en) | 1988-11-09 |
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Legal Events
Date | Code | Title | Description |
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WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |