GB2170235A - Liquid fabric softening and antistatic compositions, including detergent compositions - Google Patents
Liquid fabric softening and antistatic compositions, including detergent compositions Download PDFInfo
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- GB2170235A GB2170235A GB08602040A GB8602040A GB2170235A GB 2170235 A GB2170235 A GB 2170235A GB 08602040 A GB08602040 A GB 08602040A GB 8602040 A GB8602040 A GB 8602040A GB 2170235 A GB2170235 A GB 2170235A
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- bentonite
- isostearamide
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- 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
- C11D3/0084—Antioxidants; Free-radical scavengers
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- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/521—Carboxylic amides (R1-CO-NR2R3), where R1, R2 and R3 are alkyl or alkenyl groups
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- 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
- C11D3/0015—Softening compositions liquid
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- 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
- C11D3/1266—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in liquid 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
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/32—Amides; Substituted amides
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Biochemistry (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
A fabric softening and antistatic liquid laundry detergent composition includes synthetic anionic organic detergent, bentonite and higher aliphatic isostearamide antistat in an aqueous medium. The liquid detergent composition preferably contains a builder, such as polyphosphate and/or carbonate. A process for washing and drying laundry utilizes the described liquid detergent in the washing operation and produces laundry that is soft and static-free, or of low electrostatic charge, despite having been subjected to a tumble drying process or similar static charging drying process, which normally causes laundry of similar fabrics to become electrostatically charged, resulting in objectionable "static cling". A combined softening and antistatic composition which comprises bentonite fabric softener and N-isostearamide antistat in an aqueous medium is intended for addition to liquid detergent compositions or to wash waters. The preferred isostearamides are N-cocoisostearamide, N-octylisostearamide and N-hydrogenated tallow isostearamide.
Description
SPECIFICATION
Fabric softening and antistatic liquid detergent compositions
The present invention relates to detergent compositions. More particularly, it relates to fabric softening and antistatic liquid detergent compositions, preferably built detergent compositions, which include synthetic organic detergent, builder (preferably) for the detergent, bentonite and Nhigher aliphatic isostearamide antistatic agent in an aqueous medium. The present invention also extends to a process for washing and drying laundry which produces laundry that is soft and static-free or of low electrostatic charge despite having been subjected to a normal tumble drying operation.
Built synthetic organic detergent compositions are today the cleaning materials of choice for washing dirty laundry. Such compositions have been found to be exceptionally effective in laundering fabric items made from synthetic and/or natural fibrous materials, whether such have been stained with oily, proteinaceous or clay soils, which three soils are those most frequently encountered in home laundering, and which are fairly representative of soils normally occurring and present on usual dirty laundry.With the replacement of soap in washing compositions by synthetic organic detergents the softening effect of the soap (usually as an insoluble soap which deposited on the laundry fabric fibres) has been lost and especially in the presence of certain inorganic builder salts the laundry fabric fibres) has been lost and especially in the presence of certain inorganic builder salts the laundry will often become unpleasant to the touch, rough and stiff (or boardy). For year it has been known that bentonite, when added to synthetic organic detergents composition based on anionic detergents, could help to soften the laundry and thereby could make detergent compositions that were so modified acceptable to the consumer.
While liquid detergent composition have been known for years it was only comparatively recently that liquid state heavy duty built laundry detergent compositions become very popular.
Such formations, especially when they contain suspended solids, are sometimes thickened to prevent settling out of components, on storage. Bentonite, of the gelling type, such as Western or Wyoming bentonite, has thickening properties and additionally, is a fabric softener.
With the advent of synthetic polymeric fibres and clothing and other laundry items made from them and from blends of such synthetics with natural fibres, such as cotton/polyester blends, and with the increasing use of automatic laundry dryers, which are almost all of the tumble drying type, it was found that dried laundry often accumulated electrostatic charges that would cause it annoyingly to cling together, interfering with normal handling and with folding of the laundry for storage. Cationic compounds, such as quaternary ammonium salts, e.g. di-higher alkyl di-lower alkyl ammonium halides, have been known for years to be capable of acting as antistatic agents (antistats) to decrease static charges on fabric items and to prevent static cling.
Such quaternary ammonium halides would normally be added in the rinse water during a washing cycle, and not in a detergent composition or in the wash water, because they react chemically with anionic detergents, which are the detergents most frequently employed in synthetic organic detergent compositions. Such reaction, which would be expected to be more severe in liquid detergents than in particulate products, would diminish the detersive power of the detergent composition and could create undesirable reaction products, which could deposit on the laundry being washed, creating dirty or greasy spotting.In recent years cationic compounds, such as the quaternary ammonium halides, have been formulated into built detergent compositions, especially particulate detergent compositions, in which they do not chemically react objectionably with the anionic detergents during storage but do react to some extent with them in the wash water.
While such compositions exert an antistatic effect and diminish static cling of the washed laundry it has been noted that the detergency of the compositions in which they are present is inferior to that of the base composition without the antistat.
In accordance with the present invention a fabric softening and antistatic liquid detergent composition comprises a detersive proportion of a synthetic organic detergent, a fabric softening proportion of bentonite and an antistatic proportion of higher aliphatic isostearamide antistat, in an aqueous medium.
Liquid detergent compositions containing both bentonite and N-substituted isostearamide antistat in accordance with the present invention give a number of desirable effects. Laundry washed with such compositions is of satisfactory softness (especially towels made from fabrics woven or otherwise manufactured from natural organic vegetable fibres, such as cottons and terrycloths), of little or no static cling, there is improved detergency, and little or no "quart spots" on washed laundry. Especially noteworthy is the unexpected improvement in the antistatic effect of the N-primary aliphatic isostearamide due to the presence of the bentonite in the liquid built detergent composition (in the presence of anionic detergent).Additionally, little or no reductions in foaming power and little or no reductions in fluorescent brightening effects are noted when using the present anionic detergent compositions containing bentonite and CISA, whereas when quaternary ammonium salts are employed as antistats, foaming capabilities are diminished, appar ently due to the reaction of the quaternary salt with the anionic detergent. Furthermore, yellowing or similar discolouration of the laundry by the antistat, and soil redeposition are diminished, compared to those resulting when a quaternary ammonium halide is utilized with an anionic detergent in other built detergent composition for any antistatic properties it can contribute.
Normally, the active detergent component of the detergent compositions of the present invention will be an anionic detergent (which would be reactive with a quaternary ammonium salt), and the detergent composition will be a built composition, containing a detergent builder, such as sodium tripolyphosphate, sodium carbonate, NTA, or polyacetal carboxylate or other suitable builder, or mixture of such builders. In a preferred liquid detergent composition the isostearamide will be dissolved, emulsified or dispersed and the bentonite will be present as a finely divided dispersion, with the particles thereof preferable being smaller than No. 200, U.S. Sieve Series (which have openings 74 microns across), such as of No's. 200 to 400 sieves (which have openings 74 to 37 microns across), e.g. about No. 325 sieve (which have openings 44 microns across).If desired, the bentonite and/or N-isostearamide may be added to the wash water before, after or together with the balance of the components of the described liquid detergent composition.
The anionic synthetic organic detergents of the present detergent compositions will normally be sulphated and/or sulphonated lipophilic material(s) having an alkyl chain of 8 to 20 carbon atoms, preferably 10 to 18 and more preferably 12 to 16, and preferably will be a particular mixture of two types of such detergents. While various water soluble salt-forming cations may be used to form the desired soluble sulphated and sulphonated detergents, including ammonium and lower alkanolamine (such as triethanolamine), and magnesium, usually an alkali metal, such as sodium or potassium, is employed, and very preferably such cation will be sodium. Among the various anionic detergents that are useful in the practice of the present invention the linear higher alkybenzene sulphonates with 10 to 18 carbon atoms making up the alkyl chain, preferably 12 to 16 and more preferably about 12 to 14, e.g.dodecyl and tridecyl, are considered most suitable, often with a salt of sulphuric acid of a polyethoxylated higher fatty alcohol. The alcohol ether sulphate will normally be of a higher linear (such as fatty) alcohol of 10 to 18, preferably 12 to 15 carbon atoms, and the extent of ethoxylation will usually be 1 to 15 ethoxy groups per mole, preferably 2 to 10, more preferably 2 to 5, e.g. 3. Also, useful, among other synthetic detergents, are the monoglyceride sulphates, higher fatty alcohol sulphates, paraffin sulphonates and olefin sulphonates, in all of which compounds the alkyl group present is usually of 10 to 18 carbon atoms. Some such alkyl groups may be slightly branched (not preferred) but will still be of a carbon chain length within the described range.
Although the linear higher alkylbenzene sulphonates and the sulphated polyethoxylated higher alcohols, as the sodium salts, are the preferred anionic detergents utilized in the practice of the present invention, mixtures of such detergents with other such sulphonates and sulphates containing different cations may be employed, as may be mixtures of such detergents with others, such as the fatty alcohol sulphates. In some instances only relatively minor or diminished proportions of the linear alkybenzene sulphonates and polyethoxylate sulphates will be present or the anionic synthetic organic detergent may be a mixture of other anionic detergents of the types described.Also, various other anionic detergents may be employed, such as those which are well known in the art, which are described in various annual publications entitles McCutcheon's Detergents and Emulsifiers, for example, that which was issued in 1969.
While the present invention is primarily of anionic detergent compositions which have antistatic properties, the desirable results mentioned herein are also obtainable with compositions containing other types of synthetic organic detergents, often with the anionic detergents, such as nonionic and amphoteric detergents. The mentioned nonionic and amphoteric materials are normally present in only minor proportions, if present at all, and usually only half as much thereof will be present, at the most, as of the synthetic anionic organic detergent.Preferred nonionic detergents are the ethylene oxide condensation products of higher fatty alcohols, such as condensation products of higher fatty alcohols, such as condensation products of higher fatty alcohols of 12 to 18 carbon atoms with from 3 to 20 moles of ethylene oxide, preferably condensation products of higher fatty alcohols of 12 to 15 carbon atoms with 5 to 15 moles of ethylene oxide.
The detergent will preferably be built with a detergent builder so that it will have increased cleaning power and be suitable for "heavy duty" cleaning applications. Among useful builders for the compositions of the present invention are the polyphosphates such as sodium tripolyphosphate and tetrasodium pyrophosphate, sodium carbonate, sodium bicarbonate, sodium sesquicarbonate, sodium silicate (Na2O:SiO2= 1.6 to 3.0, preferably about 1:2.4), NTA, sodium citrate, sodium gluconate, borax, other borates, zeolites, polyacetal carboxylates and other useful builders known in the liquid detergent art. Often sodium silicates will be omitted because in liquid media they may react objectionably with carbonate and zeolite builders, and with bentonite, to produce undesirably thick or coagulated products or precipitates.
When zeolite builders are employed they will usually be of the formula (Na2O)x.(Ai203)v.(SiO2)z w H20, wherein x is t, y is from 0.8 to 1.2, preferably about 1, z is from 1.5 to 3.5, preferably 2 to 3 or about 2, and w is from 0 to 9, preferably 2.5 to 6. Such zeolites are cation exchanging and have an exchange capacity for calcium ion in the range of about 200 to 400 or more milligram equivalents of calcium carbonate hardness per gram. They will very often be hydrated to the extent of 5 to 30%, preferably 10 to 25% moisture, e.g. about 20% thereof. Zeolite A is preferred (X and Y are also useful) and for such zeolite, Type 4 A is most preferred.Practical sizes of the zeolite(s) will usually be 100 to 400 mesh (or sieve number) (which have openings 149 to 37 microns across), preferably 140 (which have openings 105 microns across) or 200 to 325 mesh, but their ultimate sizes will be submicron. The various zeolites are described at length in the text Zeolite Molecular Sieves, by Donald W. Breck, published in 1974 by John
Wiley & Sons, especially at pages 747-749 thereof.
When polyacetal carboxylates are present they may be considered to be those described in
U.S. Patent 4,144,226 and may be made by the method mentioned therein. A typical such product will be of the formula
wherein M is selected from the group consisting of alkali metal, ammonium, alkyl groups of 1 to 4 carbon atoms, tetraalkylammonium groups and alkanolamine groups, which are of 1 to 4 carbon atoms in the alkyls thereof, n averages at least 4, and R' and R2 represent any chemically stable groups which stabilize the polymer against rapid depolymerization in alkaline solution.
Preferably the polyacetal carboxylate will be one wherein M is alkali metal, e.g. sodium, n is from 20 to 200, Rt represents
or a mixture thereof, R2 represents
and n averages from 20 to 100, more preferably 30 to 80. The calculated weight average molecular weights of the polymers will normally be within the range of 2,000 to 20,000, preferably 3,500 to 10,000 and more preferably 5,000 to 9,000, e.g. about 8,000.
Although the preferred polyacetal carboxylates have been described it is to be understood, that they may be wholly or partially replaced by other such polyacetal carboxylates or related organic builder salts described in various Monsanto patents on such compounds, processes for the manufacture thereof and compositions in which they are employed. Also, the chain terminating groups decribed in the Monsanto patents referred to, especially U.S. 4,144,226, may be utilized, providing that they have the desired stabilizing properties, which allow the mentioned builders to be depolymerized in acidic media, facilitating biodegradation thereof in waste streams, but maintain their stability in alkaline media, such as washing solutions.
When it is desired to avoid the presence of phosphorus in the detergent composition polyphosphate builders may be omitted from the present formulations, in which case it is preferred to employ other non-phosphate builders, such as those mentioned herein. Combinations of zeolite and polyacetal carboxylate are very useful substitutes for the polyphosphate builders. The sodium salts of such builders are preferably employed but alkali metal and other soluble salts may be at least partially substituted for them.
Electrolytes and fillers may be present in the liquid detergent, such as sodium sulphate (preferred) and sodium chloride, to modify its physical characteristics and to add electrolyte to the product and to the wash water when such is considered to be desirable, and they may also serve other functional purposes.
The antistatic agent of choice in the practice of the present invention is N-cocoisostearamide.
Such antistatic agent is an amide which is chemically derivable from isostearic acid and cocoamine by the condensation reaction shown below:
Isostearic acid,
is a saturated fatty acid of the formula C17H3COOH, which is a complex mixture of isomers, primarily of the methyl-branched series, that are mutually soluble and virtually inseparable. While such acid normally has uses similar to those of stearic or oleic acids, it is considered that it is far superior to such materials in manufacturing effective antistatic agents, which are most suitable for incorporation in the synthetic organic anionic liquid detergent compositions according to the present invention. Cocoamine is an aliphatic amine in which the aliphatic group is derived from coconut oil.Other primary aliphatic amines, preferably higher alkylamines of 7 to 18 carbon atoms in the alkyl group, such as R'NH2, wheren R' is such a higher alkyl group, may also be used, but cocoamine produces N-alkyl isostearamide of the best properties for incorporation in detergent compositions. Such amine is named CISA.
While CISA is the most highly preferred antistatic agent (such may be referred to as antistats) it is within the broader aspects of the present invention to employ other N-aliphatic isostearamides, such as those derived from primary aliphatic amines containing up to 20 carbon atoms, preferably 7-18 carbon atoms, the aliphatic parts of which may or may not be hydrogenated, provided that the amides made have sufficient antistatic effect in the described use. Some examples thereof are the N-alkylisostearamides of 7 to 18 carbon atoms, such as N-decylamine,
N-octylamine and those derived from N-tallowamine.However, it is considered that CISA is the best of the N-alkylisostearamides in antistatic activity and therefore when the other isostearamides are used, such use will preferably be with CISA, and the proportion of other isostearamide(s) will preferably be minor, with respect to the CISA. In some cases the hydrogen atom on the amide nitrogen may be replaced by suitable radicals, such as lower alkyl, e.g. methyl, providing that a desired antistatic effect is still obtained, but it has been found that the tertiary isostearamides usually are of little antistatic activity.
The bentonite utilized is preferably a Wyoming or Western bentonite having a swelling capacity in the range of 3 to 15 ml/gram, preferably 7 to 15 ml/g, and its viscosity, at a 6% concentration in water, will usually be in the range of 3 to 30 centipoises, preferably 8 to 30 centipoises. Useful swelling bentonites of this type are sold under the trademark Mineral Colloid, as industrial bentonites, by Benton Clay Company, an affiliate of Georgia Kaolin Co. Such materials were formerly marketed under the trademark THIXO-JEL by such company. They are selectively mined and beneficiated bentonites, and those considered to be most useful are available as Mineral Colloid 101, 102, 103 and 104, and correspond to those formerly sold as
THIXO-JEL's Nos'. 1, 2, 3 and 4.These materials have pH's (6% concentration in water) in the range of 8 to 9.4, maximum free moisture contents of about 8% and specific gravities of about 2.6, and for the pulverized grade about 85% passes through a 200 mesh U.S. Sieve Series sieve. Equivalent to such bentonite is that sold as Bentonite Clay AEG 325 by Americal Colloid
Co., which is essentially of No. 325 sieve size (U.S. Sieve Series) (which has openings 44 microns across).
Beneficiated Wyoming bentonite is preferred as a component of the compositions of the present invention but other bentonites are also useful, especially when they form only a minor proportion of the bentonite used. It has been found that at least about 2%,*preferably at least 4%, and more preferably 5% or more, to about 8%, of water should be present in the bentonite initially, before it is admixed with other components and with the liquid medium for the liquid detergent. It has been established that overdrying to the point where the bentonite loses its "internal" moisture can interfere with the ability of the bentonite to hydrate effectively in aqueous medium, and can significantly diminish the fabric softening utility of the compositions of the present invention.
Among the various adjuvants that may be present in the liquid detergents of the present invention are colourants, such as dyes and pigments, perfumes, enzymes, stabilizers, thickeners, solvents, dispersants, activators, fluorescent brighteners, bleaches, buffers, fungicides, germicides, foaming agents, antifoaming agents and flow promoting agents. Also included among adjuvants, builders and fillers, unless in other classes that are mentioned, are various additional components or impurities sometimes present in the components of the compositions. For example, it is known that sodium carbonate and water are often present with polyacetal car boxylate in Builder U, a product which is a present source of polyacetal carboxylate.
Proportions of the essential components of the detergent compositions are such as to make them operative for the intended purposes of the compositions. Thus, the synthetic organic detergent or mixture thereof will be present in the liquid detergent in a detersive proportion, the bentonite will be present in a fabric softening proportion and the higher aliphatic isostearamide antistat will be present in an antistatic proportion. When the builder or builder mixture is present, as it is in most detergent compositions in accordance with the present invention, it will be present in a detergent builder proportion.The proportions described will normally be 3.5 to 25% of the liquid detergent, such as sodium linear higher alkylbenzene sulphonate, preferably 3 to 15% thereof and more preferably about 5 to 13% thereof, e.g. about 9% of sodium linear akylbenzene sulphonate of 12 to 13 or 14 carbon atoms, with 0.5 to 10% of sodium higher fatty alcohol polyethoxy ether sulphate of 8 to 18 carbon atoms in the alcohol and 1 to 15 moles of ethylene oxide per mole, preferably 1 to 5% of sodium higher primary alcohol polyethoxy ether sulphate of 12 to 15 carbon atoms in the alcohol and of 2 to 4 or 6 moles of ethylene oxide per mole, e.g. about 2%.The builder for the liquid detergent, which may be a mixture of builders, will normally be 5 to 40% of the composition, often preferably being a combination of 5 to 25% of sodium tripolyphosphate and 2 to 10% of sodium carbonate and more preferably often being a combination of 8 to 14% of sodium tripolyphosphate and 3 to 7% of sodium carbonate, e.g. about 11% and 4% respectively. The bentonite component will normally be 3 to 20% of the liquid detergent composition, preferably being 5 to 20% thereof and more preferably being about 5 to 15% thereof, e.g. about 12%, with the isostearamide antistat normally being 1 to 10% of the liquid detergent composition, preferably being 1 to 7% thereof and more preferably being about 3 to 7% thereof, e.g. about 5%.The water or aqueous medium content of the liquid detergent will usually be in the range of 3 to 80%, preferably being from 40 to 70%, more preferably being about 45 to 65%, e.g. about 55%.
In the liquid detergent composition the ratio of bentonite to antistat will usually be in the range of one part of antistat to from 1 to 20 parts of bentonite, preferably being in the range of 1:1.5 to 4 and more preferably being in the 1:2 to 3 range, e.g. about 1:2.4.
In making the liquid detergent compositions of the present invention the various components of the final product are normally merely mixed or blended together and stirred or otherwise agitated sufficiently so as to produce a uniform liquid product. Orders of addition of components may be regulated to as to promote best mixing. Sufficient liquid medium will normally be present at all times so as to prevent caking of the solids with a deficient proportion of liquid, and to prevent the creation of lumps which might subsequently be difficult to disperse. Usually finely divided particulate components, both soluble and insoluble, will be admixed with a portion of the aqueous medium, and subsequently the balance of the aqueous medium will be utilized to thin the mix, in accordance with normal manufacturing techniques.The mix may be subjected to passage through a homogenizer so as to promote dispersion of the components and to prevent settling out thereof and in some instances hydrotropic material, such as sodium cumene sulphonate and sodium xylene sulphonate, normally in small proportions, e.g. up to about 1 or 2%, may be present in the formula to help to maintain the liquid composition homogeneous. Similarly, solvents, such as ethanol and ethylene glycol or other suitable glycols may be employed to solubilize composition components, and such solvents also help to prevent freezing of the product when it is subjected to cold weather conditions. The various solid components of the liquid detergent composition that are employed will normally be in finely divided particulate state, so as to promote ready solution (when soluble) or dispersion in the aqueous medium.Usually the powdered materials will be of particle sizes less than No. 140 or No. 200, U.S. Sieve
Series, and normally such particle sizes will be mostly within the range of No's. 140 to 400, often preferably 200 to 400, e.g. about No. 325. With readily soluble components, such as sodium carbonate, sodium tripolyphosphate and the synthetic organic detergents, the particle sizes may be at the larger ends of the given ranges, or even larger, but for insoluble or slowly soluble materials, such as zeolites and clays, the smaller particle sizes are generally more desirable.
In the use of detergent compositions in accordance with the present invention, laundry is washed with a described liquid detergent composition in wash water, and such laundering is easily effected in accordance with normal laundry procedures, with standard equipment and normal washing concentrations of the liquid detergent compositions of the present invention, and the washing results in a clean wash which is soft to the touch and does not exhibit objectionable static cling, even when substantial proportions of synthetics, such as polyesters, e.g. Dacron (Registered Trade Mark), and polyamides, e.g. nylons, are present. The wash water employed may be any normal city water and the present liquid detergent compositions are effective even when the hardness is as high as 300 ppm, as calcium carbonate, and sometimes even higher.
Normally the water hardness is of mixed magnesium and calcium ions hardness, usually with the major proportion being from calcium. Preferably the wash water will be of a hardness no greater than 250 ppm and usually city waters employed will have hardnesses from 20 to 150 or 200
ppm, e.g. about 50 or 100 ppm. The present compositions may be used with wash waters at
any of various temperatures (10 to 900C), and are effective even with wash waters at lower temperatures, such as about room temperature. Following European practice, the compositions
may be used in wash waters at temperatures which may approach boiling, e.g. 70" to 90"C, but in usual American practice lower temperatures are utilized.Especially good results are obtained,
in American washing practice, by employing the present compositions in wash waters at temperatures in the range of 10 to 50or, preferably 30 to 50 C, e.g. about 40"C. The concentration of the liquid detergent composition in the wash water may be varied, depending on circumstances,
but normally will be in the range of 0.1 to 0.5% by weight, preferably 0.1 to 0.4% and more
preferably 0.15 to 0.25%, e.g. about 0.2%. Thus, one-half cup or 145 g of the liquid detergent,
often of a density of about 1.1 to 1.3 g/ml, e.g. about 1.2 g/ml, may be employed in a
washing machine containing about 65 litres of water, to wash a normal load, which is about 2.7 to 4.5 kg, e.g. about 3.6 kg, of dry laundry.In some instances, as when it is desired that the
liquid detergent be such that greater or lesser volumes will be employed per wash load, the
concentrations of the components in the liquid composition can be increased or decreased
accordingly, within practical limits.
Standard home laundry washing machines and the normal wash cycles of such machines may
be used, or industrial or commercial washing machines may be employed. Washing of the
laundry is effected in a normal cycle over a period of about 2 to 30 minutes, such as 5 to 20
minutes, e.g. about 10 minutes, usually depending on the dirtiness of the laundry and the nature
of the fabric. After completion of the washing cycle the laundry is automatically rinsed, and is
subsequently dried in an automatic laundry dryer, in which it is tumbled while being subjected to the passage of drying air through it.
Instead of a liquid detergent which includes all of the described detersive, building, fabric
softening and antistatic components of the compositions of the present invention, in a variation
of the present invention a liquid composition may be made comprising fabric softening and
antistatic components, and such composition may be utilized in conjunction with a suitable liquid
detergent, such as any of many such products on the market, to impart fabric softening and
antistatic properties to laundry washed with such detergent.Thus, CISA or other suitable N
primary aliphatic isostearamide and bentonite (or other suitable fabric softening clay) may be
emulsified, dispersed, suspended and/or partially dissolved in a suitable liquid medium, preferably
aqueous, with a minor proportion of hydrotrope, emulsifying agent, suspending agent and/or
solvent to produce a suitable pourable liquid preparation which can be employed in supplementa
tion of the liquid detergent. Such liquid preparation can be added to the liquid detergent
beforehand and/or may be added to the washing medium together with the liquid detergent, or
it may be added to compositions of the present invention or to the wash water with such
compositions so as further to improve the softness and antistatic properties of washed laundry.
Utilizing such a fabric softening and antistatic supplemental composition one is able to adapt the
present invention to employment with any of various liquid detergent formulations. Thus, it is left
to the consumer to determine, within reason, how much softening and antistatic effects are to
be imparted to the laundry and it is possible to employ more of the supplement when utilizing
detergent compositions which are especially effective (or harsh) detergents, requiring greater
softening and more antistat treatment. Normally, in the supplementing liquid compositions de
scribed the proportion of combined fabric softener and antistat present will be from 10 to 30%,
but from 10 to 50% is feasible, especially if a co-solvent, such as ethanol, is present.The
proportion of antistat to bentonite will be in the same range(s) as previously given for the
described liquid detergent compositions containing both antistat and softener.
Various advantages of the invention, some of which were previously alluded to, will be clearly
illustrated in the working examples, which follow. The N-primary aliphatic isostearamide antistat
does not react objectionably with bentonite nor does it so react objectionably with bentonite nor
does it so react with the anionic detergents, and therefore, compositions of the present inven
tion are comparatively stable on storage and do not lose significant proportions of their desired
detersive, softening and antistat activities on storage or before or in use.Unlike compositions
based on the usual currently employed cationic fabric softeners and antistatic agents, such as
quaternary ammonium salts, the present compositions do not deposit reaction products of such cationic materials and anionic detergents onto laundry being washed, so such laundry is not as
subject to soil deposition during washing processes when the present invention is employed.
The detergent compositions of the present invention produce whiter laundry and less soil
redeposition too, whereas laundry washed with compositions containing anionic detergent and
quaternary ammonium salt (in antistat and fabric softener proportions) tend to become yellower,
especially on repeated washings. Detergency is measurablay better when the compositions of
the present invention are employed than when those are used in which a quaternary ammonium
salt is present instead of the isostearamide. Also, interference with the foaming power of the
anionic detergent, usually noted when cationics, such as quaternary ammonium salts, are pre
sent, and reactions of such "quats" with fluorescent brighteners, and resulting diminished brightening of laundry, are avoided when the present antistats are used.Such undesirable interactions of anionic and cationic materials are especially serious and objectionable when both the anionic detergents and the cationic softener-antistats are present for comparatively long periods of time in intimate contact, as they are when they are in the same aqueous medium, such as in some fabric softening anionic liquid detergents. It is evident that the present invention represents a significant improvement in the detergent art, wherein today it is important that detergent compositions possess fabric softening and antistatic properties, in addition to excellent detergency.
The liquid detergents of the present invention and the liquid supplements described above are both preferably sufficiently viscous or (thixotropic) as to maintain finely divided particulate components in suspension and to prevent settling out thereof on storage, and yet the liquids should be freely flowable through a relatively narrow necked dispensing opening of a container such as a bottle. It has been found that liquids of viscosities within the range of 1,000 to 5,000 centipoises usually do not settle out and they possess the desired flow characteristics. Accordingly, the liquids of the present invention will desirably be of a viscosity in such a range.More preferably, such range may be from 3,000 to 5,000 cps, e.g. about 4,000 cps, at room temperature (25"C). While it is considered that the viscosities of the compositions of the present invention are comparatively stable it is recognised that relatively small changes in plant manufacturing processes and changes in storage conditions may influence the viscosity of the product, which more frequently increases, rather than decreases on storage. If the viscosity or thickness increase excessively it will usually be found that placement of a case of packed bottles in a shaking machine will almost always make the composition flowable from the bottle and will disperse any components which may have separated out.
The invention may be put into practice in various ways and a number of specific embodiments will be described to illustrate the invention with reference to the accompanying examples. Unless otherwise indicated, all parts are by weight and all temperatures are in "C in the examples, in the specification, and in the appended claims.
EXAMPLE 1
A liquid detergent composition is made up having the composition given in Table 1 below.
TABLE 1
Component Percent
Sodium linear tridecylbenzene sulphonate 9.0
Sodium primary higher alcohol ether sulphate1 2.0
Bentonite (American Colloid Company AEG 325) 12.0
Sodium tripolyphosphate 11.0
Sodium carbonate 4.0
N-cocoalkyl isostearamide 5.0
Optical brightener (Tinopal LMS X [CIBA 0.3
GEIGY])
Sodium carboxymethyl cellulose 0.2
Dye (Polar Brilliant Blue, 1% aqueous 0.6
solution)
Perfume 0.5
Deionized water 54.7
100.0
Note on Table 1
Reaction product of primary alcohol of 12 to 15 carbon atoms and 3 moles of ethylene oxide per mole.
The detergent components are dissolved in 2/3 of the formula water, after which the CISA is dispersed and dissolved in the detergent solution thus made, and the builder salts are dissolved in such aqueous medium, after which the bentonite in finely divided particulate form is dispersed in the composition, followed by additions of the various adjuvants and the balance of the water.
The product resulting is of a viscosity about 3,000 centipoises at 25"C, using a Brookfield viscometer with a No. 3 spindle at a speed of 12 r.p.m. The detergent composition is stable, with the components thereof remaining dissolved-dispersed in the aqueous medium and not settling out or otherwise separating.
A mixed fabric load of 3.6 kg of laundry made from various materials (polyester, nylon, acetate and polyester-cotton blend) is washed in a conventional G.E. top loading washing machine, containing 65 litres of water of 100 ppm hardness, as calcium carbonate, of mixed calcium and magnesium ions, using 145 grams of the liquid detergent composition of the above formula, and the washed laundry, including test swatches of the different materials mentioned, is rinsed and subsequently is dried in an automatic laundry dryer of the tumble drying type. The softness of the various fabrics is evaluated by expert evaluators and the protection of each of the fabrics against generation of electrostatic charge (and objectionable static cling) on tumble drying and during other motion is also evaluated, by noting the extent of static cling exhibited by the individual laundry items.The washed laundry is satisfactorily soft and non-clinging.
Quantitative measurements of the electrostatic charge pick-ups by the different washed and dried fabrics are obtained by rubbing each of the fabrics with wool in a controlled manner at a low relative humidity (25 to 30% R.H.) and measuring the charges accumulated by the swatches.
In this test a plurality of swatches is employed and average readings for each material are computed, To obtain an antistat index representing an overall evaluation of the antistat capability of a liquid detergent composition, it has been found useful to employ the sums of the charges on the mentioned materials. Thus, such sum for the present liquid detergent is 12 kilovolts whereas for a control liquid detergent of the same formula but omitting bentonite and CISA, the index is 48 kilovolts. For the present tests readings in excess of 35 kilovolts are usually unacceptable (the laundry will cling objectionably).When evaluated for softness (terrycloth towels are the laundered test items) by a panel of experienced evaluators for this property in laundry, the towels washed with the liquid detergent composition of this example according to the method described above are rated 9 for softness on a scale of 1-10, with 10 being the softest.
Towels washed with the control composition in the same manner are rated 1.
In other tests made the extent of redeposition of soil on the washed laundry is found to be about the same with the product of the present invention as with a second control product, which is like the formula in Table 1 except for replacement of the N-alkyl isostearamide with water, and such redeposition is worse (more) for a third control detergent composition, like the composition of Table 1 except for replacement of the isostearamide with the same percentage of dimethyldistearyl ammonium chloride.
The test cloths and laundry washed with the product of the present invention show no "quatspotting", which sometimes is noted on laundry washed with similar formulas containing dimethyldistearyl ammonium chloride or other quaternary compound instead of the N-isostearamide antistat. Also, the optical brightening effect for the product of the present invention containing
N-isostearamide is greater than that for a similar product, in the formula of which the isostearamide is replaced by dimethyldistearyl ammonium chloride or other such antistatic quaternary ammonium halide. Another advantage of using CISA instead of the "quat" is an improvement in the appearance of the liquid detergent composition due to the absence of any precipitated product from reaction of the quat and the anionic detergent.
When, in the formula given in Table 1, the 5% of N-cocoalkyl isostearamide is replaced by 1%, 3% and 7%, respectively, of such isostearamide, the softness evaluations of the products resulting are 8, 8 and 9, respectively, and the static indices are 27, 19 and 10, respectively.
Softness indices of 8 or above are considered satisfactory, as are static indices of less than 30, with softness indices as low as 7 and static indices as high as 35, sometimes being rated acceptable. When CISA is omitted from the formula, as in the second control, the washed laundry is given a softness rating of 8 and the electrostatic charge index is 36 kilovolts.
When in practical laundry tests the first control and the composition of Table 1 are compared, it is found that the control does not satisfactorily soften laundry and produces high electrostatic charges and objectionable static cling. When bentonite is omitted from the formula of Table 1, as in the fourth control, the detergent compositions are unsatisfactory with respect to both softening power and inhibition of static cling, even when a comparatively high proportion of the isostearamide is present. When the isostearamide is omitted objectionable static cling of washed laundry is observed despite the presence of 12% of bentonite.Thus, it is seen that the combination of bentonite and N-higher alkyl isostearamide is important to the success of the laundry detergent composition of the present invention because: 1) such combination leads to obtaining greater antistatic action than would be predictable; 2) the bentonite softens laundry; and 3) both fabric softening and antistatic (anti-cling) properties are now required of detergent compositions by discriminating consumers.
Instead of the preferred N-cocoalkyl isostearamide other higher aliphatic isostearamides, preferably higher primary aliphatic isostearamides, and more preferably higher primary N-alkyl isostearamides, may be utilized, such as N-n-octyl isostearamide, N-n-decyl isostearamide, N-n-heptyl isostearamide, N-n-dodecyl isostearamide, N-n-tetradecyl isostearamide and N-primary hydrogenated tallow isostearamide.
When the bentonite content of the formula given in Table 1 is modified within the 3 to 20% range, as to 10%, 15% and 18%, useful softening and antistatic detergent compositions result, and even when the bentonite content is increased to 5% noticeable fabric softening is still obtainable. Similarly, changes in the proportion of anionic detergent may be made within the range of 3.5 to 25%, e.g. 5%, 15% and 25%, and the total proportion of builder salt may be varied within the 5 to 40% range, e.g. 10, 20 and 30%, and effective softening and antistatic detergent compositions can result. In all such compositions water will constitute the balance, except for any adjuvant(s) present, which will usually be limited to no more than 10%.
The bentonite utilized may be changed to any of the other types of bentonite mentioned previously in the specification, and sometimes other useful swelling clays, such as other mont morillonites may be used, but usually it will be preferable to employ Western or Wyoming type of bentonite. The sodium linear tridecylbenzene sulphonate may be replaced either in whole or in part by sodium linear dodecyl-benzene sulphonate or other linear higher alkylbenzene sulphonate of 10 to 15 or 18 carbon atoms, or with other anionic detergent, such as sodium lauryl sulphate, sodium cetyl sulphate, sodium paraffin sulphonate, wherein the paraffin is of about 16 carbon atoms, and/or sodium cocomonoglyceride sulphate, or any of various mixtures thereof.
The ether sulphate may be replaced with other similar detergents, such as sodium dodecyl pentaethoxy sulphate, or with other(s) of the anionic detergents previously mentioned. Other builders may be substituted for the polyphosphate and carbonate, such as those previously named, and non-phosphate detergents can thus be prepared.
In the described variations, within the invention, of the preferred lead formula the products obtained are useful fabric softening and antistatic detergent compositions and are superior, in the properties previously described, to formulations from which the bentonite and isostearamide have been omitted and from formulations in which quaternary ammonium salts are employed instead of the isostearamide.
EXAMPLE 2
Instead of making the complete fabric softening and antistatic liquid detergent composition described in the formula of Example 1, in a variation of the present invention a combined fabric softening and antistatic composition, is made, comprising bentonite and N-primary higher aliphatic isostearamide (CISA), in a liquid, aqueous medium. Such a liquid composition is made by merely mixing 14.1 parts of American Colloid Company AEG 325 Bentonite and 5.9 parts of Ncocoalkyl isostearamide with 80 parts of deionized water (although city water may do if deionized water is not available). The Example 1 bentonite: isostearamide ratios may also be employed.Due to the thickening action of the swelling bentonite component the powdered Nisostearamide is held suspended in the aqueous medium and the combined softening and antistatic composition is ready for bottling, shipping, storage, sale and use without further formula modifications. However, a co-solvent, such as ethanol or hexylene glycol may be included to promote dissolving of the N-isostearamide (and to act as an anti-freeze), in which case a sufficient proportion of either or both of ethanol and hexylene glycol will be employed to promote solubility and prevent freezing. Also, about 1% of sodium xylene sulphonate as a hydrotrope, may be included in the formula, with or without 0. 1 to 2% of sodium polyacrylate to disperse and/or suspend the bentonite in the aqueous system.Similarly, colourants, antioxidants, buffers, gums, antiredeposition agents (sodium carboxymethyl cellulose), optical brighteners, and perfumes may be included in the formula, in normal adjuvant proportions, most of which will be under 2% and often under 1%.
The combined softening and antistatic composition may be added by either the manufacturer or the consumer to another liquid detergent composition to improve the fabric softening antistatic properties of such composition. The proportion of the combined softening and antistatic composition being added to the liquid detergent will be such that the added material will exert fabric softening and antistat actions when the improved detergent composition is utilized. Because of the diluting effect of the combined softening and antistatic composition it will generally be desirable for more of the improved detergent composition to be used. Alternatively, the concentrations of active components in the combined softening and antistatic composition will be kept as high as reasonably possible to obtain optimum softening and antistat effects.Also, the liquid combined softening and antistatic composition may be added directly to the wash water in the washing machine, with the liquid detergent. By either of such methods of use any of various commercial built synthetic organic anionic liquid detergent compositions may be improved in fabric softening and antistatic effects. Also, it is contemplated as within the scope of the present invention to utilize this liquid combined softening and antistatic composition as a means of adding softening and antistatic properties to laundry washed with any of various different synthetic detergent compositions, particulate as well as liquid, and nonionic or amphoteric, as well as anionic.This aspect of the present invention is operative with all of the best known commercial built synthetic organic detergent products, and, as was previously indicated, such improvement is not at the expense of cleaning, brightening and other desirable properties of such detergent compositions.
EXAMPLE 3
A washing proportion of the composition of the formula given in Table 1 of Example 1 is used to wash a standard load of laundry in a conventional General Electric top loading home laundry washing machine. Alternatively, a washing proportion (120 g) of liquid detergent composition (like the first control, without bentonite and CISA) is added to the wash water, followed by separate additions of the formula proportions of 17.6 g of bentonite and 7.4 g of Ncocoalkyl isostearamide (which may be dispersed in, dissolved in or blended with a suitable liquid medium or particulate carrier, and preferably are in 125 g of a combined softening and antistatic composition as described in Example 2).The machine is filled with 65 litres of city water of a hardness of about 100 ppm, as calcium carbonate, of mixed magnesium and calcium hardness, with the calcium hardness being the major hardness. The wash water is at a temperature of 40"C and the charge of dirty laundry to the wash water is about 3.6 kilograms. The laundry washed is made of cotton, mixed cotton-polyester, acetate and polyamide (nylon), and is soiled with normal soils. Washing is continued over a period of ten minutes, after which the laundry is automatically rinsed and spin dried. It is then dried in an automatic laundry dryer, in which it is tumbled while being subjected to the passage of hot drying air through it. After drying, the laundry is evaluated by a panel of trained evaluators and is found to be satisfactorily clean, soft to the touch and free of annoying static cling.When the control detergent composition, which does not contain bentonite or the N-substituted isostearamide in its formula, is similarly used (but alone) to wash similar laundry its cleaning power is satisfactory but the laundry is noticeably harsh in feel and is subject to static cling, with the static cling being especially noticeable for the laundry items which include synthetic polymer fibres in the fabrics thereof.
EXAMPLE 4
Instead of employing the composition of Example 2 to improve a liquid detergent composition and instead of adding it to the wash water, it may also be used as a rinse water softener and antistat. In this embodiment of the present invention the liquid combined softening and antistatic composition may be added to the rinse after washing the laundry with a conventional detergent composition. Normally the charge of the combined softening and antistatic composition will be that which is sufficient to impart to the washed laundry discernible antistatic and softening effects. For example, normally the charge to the rinse water will be from 0.05 to 0.5%, preferably 0.1 to 0.3%, e.g. 0.2%.In a typical example of this embodiment of the present invention the laundry will be washed in the manner described in Example 1 with a detergent composition like that of that example except for the replacements of the bentonite and CISA with water (a small proportion of gum or other thickener may have been added to the liquid to adjust the viscosity, if desired, e.g. 0.1 to 1% of CMC, PVA (polyvinyl alcohol), PVP (polyvinyl pyrrolidone) or other gum known for this purpose).After washing of the laundry, which may be a normal charge of mixed cotton and synthetic polymeric fabrics laundry, the Example 2 combined softening and antistatic composition, containing 14.1 parts of bentonite and 5.9 parts of
CISA in 80 part of deionized water, is added to the rinse water in a 0.2% concentration (130 grams per B5 litres of the 1000 ppm hardness rinse water). The laundry is subsequently dried, sometimes after plural rinsings, and will be found to be of low static charge after machine drying, and will be softer than control laundry that is not subjected to the described rinse treatment.
The invention has been described with respect to various illustrations and embodiments thereof but is not to be considered as being limited to these because it is evident that one of skill in the art, with the present specification before him or her, will be able to utilize substitutes and equivalents without departing from the invention.
Examples A to C below illustrate the manner in which isostearamide antistat compounds usable compositions in accordance with the present invention may be prepared.
EXAMPLE A
Preparation of N-Octylisostearamide.
209 of isostearic acid, 10.1 g of thionyl chloride are mixed under nitrogen gas and 0.2 ml of dimethyl formamide (catalyst) is added. This mixture is stirred for 20 minutes on a warm water bath, charged with nitrogen gas and stirred for another 10 minutes. Infrared spectra readings shows some acid peaks still present. Additional thionyl chloride is added and the mixture stirred for another 10 minutes. Infrared readings show negligable acid peaks. The resultant product is isostearoyl chloride. The resultant isostearyl chloride is added to 11 g (0.85 mole) of noctylamine and 10 g (0.09) of triethylamine in 100 ml ether. The reaction mixture is stirred for 15 minutes at room temperature, extracted with ether, washed twice with a 5% HCI (aqueous hydrochloric acid) solution, and then water, until neutral, yielding 22 g of an amber oil which exhibits infrared spectra values typical of a secondary amide.
Example B
Preparation of N-Cocoalkylisostearamide.
256 g (0.9 Mole) of isostearic acid, 128 g (1.08 mole) of thionyl chloride and 4.5 ml of dimethylformamide are placed in a flask surrounded by a warm water bath and stirred under nitrogen for 30 minutes. At this time an infrared spectrum indicated no unreacted acid. The HCI (hydrogen chloride) formed in this reaction is blown out with nitrogen. After 30 minutes, the reaction mixture is heated in a vacuum to remove excess thionyl chloride, and distilled to recover the isostearoyl chloride which is collected at 140-150"C and 0.2 mm pressure, giving yield of 242 g (89 /a of theory).
The isostearyl chloride (54 g) is added in about 25 minutes to 37 g of cocoamine (C10-C,4), 250 ml of methylene chloride and 25 ml of triethylamine, while maintaining the temperature are below 25"C. After complete addition of the isostearoyl chloride, the mixture is stirred at room temperature for 30 minutes. The reaction mixture is transferred to a separatory funnel and washed twice with a 25% alcohol water mixture, then washed twice with 5% HCI (aqueous hydrochloric acid) and again twice with the alcohol water mixture until neutral to pH paper. The reaction product is dried over sodium sulphate and evaporated on a rotary evaporator to 79 g of a thick oil of cocoisostearamide. The infrared spectrum shows strong absorption at 3280, 1642 and 1548 cm 1 typical of a secondary amide.
Example C
Preparation of Hydrogenated Tallo wisostearamide.
Isostearoyl chloride is prepared from 56 g (0.02 mole) of isostearic acid, 25 g (0.21 mole) of thionyl chloride, 1 ml of dimethylformamide (0.014 mole) and 50 ml of methylene chloride (solvent for the reaction), by stirring the mixture, without heating or cooling, for 30 minutes, and for another 30 minutes on a warm water bath. Infrared spectra readings show no carboxylic absorption, indicating completion of the reaction. The amount of the isostearoyl chloride recovered is 70 g.
35 g of the aforesaid isostearoyl chloride is added to 27 g of hydrogenated tallow amine, 11 g of triethylamine and 150 ml of methylene chloride. The resultant N-tallowisostearamide is washed twice with a 25% alcohol water mixture, washed once with a water solution containing 25% ethanol and 5 ml of concentrated HCI and again with the 25% alcohol water mixture until neutral, is filtered and dried over sodium sulphate.
Claims (23)
1. A fabric softening and antistatic liquid laundry detergent composition which comprises a detersive proportion of a synthetic anionic organic detergent, a fabric softening proportion of bentonite and an antistatic proportion of N-higher aliphatic isostearamide antistat, in an aqueous medium.
2. A liquid detergent composition as claimed in Claim 1 which contains a detergent building proportion of a detergent builder and in which the detergent is of the sulphate and/or sulphonate type(s).
3. A liquid detergent composition as claimed in Claim 2 in which the detergent builder is selected from the group consisting of polyphosphate, carbonate, bicarbonate, sesquicarbonate, silicate, zeolite, citrate, nitrilotriacetate and polyacetal carboxylate builders, and mixtures thereof.
4. A liquid detergent composition as claimed in any one of Claims 1 to 3 which comprises about 3.5 to 25% of sulphate and/or sulphonate detergent, about 3 to 20% of bentonite, about 1 to 10% of isostearamide, about 5 to 40% of builder and about 30 to 80% of water.
5. A liquid detergent composition as claimed in Claim 4 which comprises 3 to 15% of sodium linear higher alkyl benzene sulphonate, 0.5 to 10% of sodium higher fatty alcohol polyethylene ether sulphate in which the higher fatty alcohol moiety is of 8 to 18 carbon atoms and in which the polyethoxy ether moiety is of 3 to 30 moles of ethylene oxide per mole of such detergent, 3 to 20% of bentonite, 1 to 10% of N-higher aliphatic isostearamide in which the higher aliphatic group is a primary hydrocarbon chain containing 7 to 1 8 carbon atoms, 5 to 25% of sodium tripolyphosphate, 2 to 10% of sodium carbonate and 40 to 70% of water.
6. A liquid detergent composition as claimed in Claim 5 which comprises 5 to 13% of sodium linear higher alkylbenzene sulphonate wherein the higher alkyl group is of 12 to 14 carbon atoms, 1 to 5% of sodium higher primary alcohol polyethoxy ether sulphate wherein the higher primary alcohol moiety is of 12 to 1 5 carbon atoms and the polyethoxy ether moiety is of 6 to 20 moles of ethylene oxide per mole of such detergent, 5 to 15% of bentonite, 1 to 7% of N-primary higher alkyl isostearamide wherein the higher alkyl group is of 7 to 18 carbon atoms,8 8 to 14% of sodium tripolyphosphate, 3 to 7% of sodium carbonate, 0.1 to 1% of sodium carboxymethyl cellulose and 45 to 65% of water.
7. A detergent composition as claimed in Claim 6 which comprises about 9% of sodium linear higher alkybenzene sulphonate wherein the higher alkyl group is of 12 to 13 carbon atoms, about 2% of sodium primary alcohol polyethoxy ether sulphate wherein the primary alcohol is of about 12 carbon atoms and the polyethoxy ether moiety is of about 1 5 moles of ethylene oxide per mole of such detergent, about 12% of bentonite, about 5% of N-cocoalkyl isostearamide, about- 11% of sodium tripolyphosphate, about 4% of sodium carbonate, about 0.2% of sodium carboxymethyl cellulose, about 1.5% of adjuvants and about 55% of water.
8. A detergent composition as claimed in Claim 1 substantially as specifically described herein with reference to the examples.
9. A process for washing laundry and simultaneously softening it and lowering its capacity to generate and/or hold an electrostatic charge, which comprises washing the laundry in an aqueous medium containing a detersive proportion of a liquid laundry detergent composition as claimed in any one of Claims 1 to 8, rinsing the laundry and drying it in an automatic laundry dryer.
10. A process as claimed in Claim 8 in which the concentration of detergent composition in the wash water is in the range of 0.1 to 0.4%.
11. A process as claimed in Claim 9 or Claim 10 in which the water temperature is in the range of 10 to 90"C and the water is of a hardness up to 300 ppm, as calcium carbonate.
12. A process as claimed in Claim 11 in which the concentration of the liquid detergent composition in the wash water is about 0.2%, the wash water is of a hardness in the range of 50 to 200 ppm, as calcium carbonate, and the wash water temperature is in the range of 30 to 50"C.
13. A liquid fabric softening and antistatic product for addition to detergent compositions or wash waters to impart fabric softening and antistatic properties to laundry washed with them which comprises a fabric softening proportion of bentonite and an antistatic proportion of Nhigher aliphatic isostearamide antistat in a liquid medium.
14. A product as claimed in Claim 13 in which the bentonite is a swelling bentonite, the antistat is N-higher alkyl isostearamide, the liquid medium is an aqueous medium and the isostearamide:bentonite proportion is in the range of 1:1.5 to 1:5.
15. A product as claimed in Claim 14 in which the bentonite is a Western or Wyoming bentonite, the isostearamide is CISA, and the total content of isostearamide and bentonite is in the range of 10 to 30%.
16. A product as claimed in any one of Claims 13 to 15 free of synthetic organic detergent.
17. A product as claimed in Claim 13 substantially as specifically described herein with reference to the examples.
18. A process for treating laundry to soften it and lower its capacity to generate and/or hold an electrostatic charge, which comprises treating the laundry with a composition comprising a softening proportion of bentonite and an antistatic proportion of N-higher aliphatic isostearamide.
19. A process as claimed in Claim 18 in which the treatment is effected in a rinsing operation after washing of the laundry and the bentonite and N-higher aliphatic isostearamide are in a liquid composition.
20. A process as claimed in Claim - 19 in which the liquid composition comprises about 1 to 10% of N-higher aliphatic isostearamide, about 3 to 20% of bentonite and about 30 to 80% of water, the N-higher aliphatic isostearamide is CISA, and the proportion of the liquid composition in the rinse water is in the range of 0.05 to 0.5%.
21. A softening and antistatic liquid composition, suitable for addition to rinse water to soften laundry and render it antistatic, which comprises about 1 to 10 parts of N-higher aliphatic isostearamide and about 3 to 20 parts of bentonite in an aqueous medium, with the proportion of bentonite to the isostearamide being in the range of 1:1 to 20:1.
22. A liquid composition as claimed in Claim 21 in which the aqueous medium is water and the isostearamide is N-primary higher alkyl isostearamide.
23. A liquid composition as claimed in Claim 21 or Claim 22 which comprises about 14 parts of bentonite and about 6 parts of CISA in about 80 parts of water.
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US69515885A | 1985-01-28 | 1985-01-28 |
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Cited By (8)
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FR2006373A1 (en) * | 1968-04-17 | 1969-12-26 | Saline Water Conversion | |
FR2616796A1 (en) * | 1987-06-17 | 1988-12-23 | Colgate Palmolive Co | NONAQUEOUS LIQUID TISSUE TREATMENT AND LAUNDRY COMPOSITIONS COMPRISING ORGANOPHILIC CLAY, SINGLE USE LAUNDRY DETERGENT PACKAGE, AND UNIT LAUNDRY DETERGENT ARTICLES CONTAINING SAME |
FR2618157A1 (en) * | 1988-07-15 | 1989-01-20 | Colgate Palmolive Co | Stable non-aqueous suspension containing an organophilic clay and a low-density filler |
EP0381487A1 (en) * | 1989-02-02 | 1990-08-08 | BP Chemicals Limited | Detergent formulations |
US5002688A (en) * | 1987-05-11 | 1991-03-26 | Lever Brothers Company, Division Of Conopco, Inc. | Detergent liquid processing |
US5021195A (en) * | 1988-02-10 | 1991-06-04 | Lever Brothers Company | Structured aqueous detergent compositions containing salting-out electrolytes and surfactants and methods of forming them |
BE1004196A4 (en) * | 1987-07-15 | 1992-10-13 | Colgate Palmolive Co | SUSPENSION CONTAINING NONAQUEOUS organophilic clay STABLE AND LOW DENSITY DEPENDENT. |
GB2361929A (en) * | 2000-05-05 | 2001-11-07 | Procter & Gamble | Liquid detergent compositions |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4626364A (en) * | 1985-01-28 | 1986-12-02 | Colgate-Palmolive Company | Particulate fabric softening and antistatic built detergent composition and particulate agglomerate for use in manufacture thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4497715A (en) * | 1982-08-03 | 1985-02-05 | Colgate-Palmolive Company | N-Alkylisostearamides as antistatic agents |
US4469605A (en) * | 1982-12-13 | 1984-09-04 | Colgate-Palmolive Company | Fabric softening heavy duty liquid detergent and process for manufacture thereof |
GB8320154D0 (en) * | 1983-07-26 | 1983-08-24 | Wilkinson Sword Ltd | Soap compositions |
US4626364A (en) * | 1985-01-28 | 1986-12-02 | Colgate-Palmolive Company | Particulate fabric softening and antistatic built detergent composition and particulate agglomerate for use in manufacture thereof |
-
1986
- 1986-01-14 ZA ZA86282A patent/ZA86282B/en unknown
- 1986-01-15 SE SE8600154A patent/SE8600154L/en not_active Application Discontinuation
- 1986-01-15 IN IN39/DEL/86A patent/IN170201B/en unknown
- 1986-01-21 NZ NZ214889A patent/NZ214889A/en unknown
- 1986-01-22 AU AU52634/86A patent/AU596089B2/en not_active Ceased
- 1986-01-23 DE DE19863601925 patent/DE3601925A1/en not_active Withdrawn
- 1986-01-24 PH PH33324A patent/PH23517A/en unknown
- 1986-01-24 PT PT81897A patent/PT81897B/en not_active IP Right Cessation
- 1986-01-27 NO NO860284A patent/NO860284L/en unknown
- 1986-01-27 ZW ZW19/86A patent/ZW1986A1/en unknown
- 1986-01-27 MX MX1363A patent/MX162392A/en unknown
- 1986-01-27 LU LU86267A patent/LU86267A1/en unknown
- 1986-01-27 FI FI860375A patent/FI85720C/en not_active IP Right Cessation
- 1986-01-27 FR FR868601088A patent/FR2576604B1/en not_active Expired - Lifetime
- 1986-01-27 IT IT47581/86A patent/IT1190454B/en active
- 1986-01-27 ES ES551261A patent/ES8800715A1/en not_active Expired
- 1986-01-27 BR BR8600312A patent/BR8600312A/en unknown
- 1986-01-28 ZM ZM8/86A patent/ZM886A1/en unknown
- 1986-01-28 NL NL8600192A patent/NL8600192A/en not_active Application Discontinuation
- 1986-01-28 AT AT0019886A patent/ATA19886A/en not_active Application Discontinuation
- 1986-01-28 GR GR860251A patent/GR860251B/en unknown
- 1986-01-28 CH CH1864/88A patent/CH673468A5/de not_active IP Right Cessation
- 1986-01-28 EG EG42/86A patent/EG17689A/en active
- 1986-01-28 CH CH1865/88A patent/CH673466A5/de not_active IP Right Cessation
- 1986-01-28 BE BE0/216183A patent/BE904113A/en not_active IP Right Cessation
- 1986-01-28 JP JP61016672A patent/JPS61176700A/en active Pending
- 1986-01-28 IE IE860232A patent/IE860232L/en unknown
- 1986-01-28 DK DK41486A patent/DK41486A/en not_active Application Discontinuation
- 1986-01-28 GB GB8602040A patent/GB2170235B/en not_active Expired
- 1986-01-28 CH CH337/86A patent/CH668267A5/en not_active IP Right Cessation
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2006373A1 (en) * | 1968-04-17 | 1969-12-26 | Saline Water Conversion | |
US5002688A (en) * | 1987-05-11 | 1991-03-26 | Lever Brothers Company, Division Of Conopco, Inc. | Detergent liquid processing |
FR2616796A1 (en) * | 1987-06-17 | 1988-12-23 | Colgate Palmolive Co | NONAQUEOUS LIQUID TISSUE TREATMENT AND LAUNDRY COMPOSITIONS COMPRISING ORGANOPHILIC CLAY, SINGLE USE LAUNDRY DETERGENT PACKAGE, AND UNIT LAUNDRY DETERGENT ARTICLES CONTAINING SAME |
BE1004194A3 (en) * | 1987-06-17 | 1992-10-13 | Colgate Palmolive Co | LIQUID COMPOSITIONS NONAQUEOUS TREATMENT OF FABRICS AND LAUNDERING, INCLUDING organophilic clay, DETERGENT LAUNDRY PACKAGE A SINGLE PURPOSE, AND THE UNIT LAUNDRY DETERGENTS CONTAINING. |
BE1004196A4 (en) * | 1987-07-15 | 1992-10-13 | Colgate Palmolive Co | SUSPENSION CONTAINING NONAQUEOUS organophilic clay STABLE AND LOW DENSITY DEPENDENT. |
US5021195A (en) * | 1988-02-10 | 1991-06-04 | Lever Brothers Company | Structured aqueous detergent compositions containing salting-out electrolytes and surfactants and methods of forming them |
FR2618157A1 (en) * | 1988-07-15 | 1989-01-20 | Colgate Palmolive Co | Stable non-aqueous suspension containing an organophilic clay and a low-density filler |
EP0381487A1 (en) * | 1989-02-02 | 1990-08-08 | BP Chemicals Limited | Detergent formulations |
GB2361929A (en) * | 2000-05-05 | 2001-11-07 | Procter & Gamble | Liquid detergent compositions |
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PCNP | Patent ceased through non-payment of renewal fee |