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
  • C11D9/00—Compositions of detergents based essentially on soap
  • C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
• • 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
• • 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

Definitions

• This invention relates to a liquid detergent composition, in particular to a liquid detergent composition for washing fabrics and imparting a softness thereto.
• British Patent Specification No GB 2 132 629-A describes a fabric softening heavy duty liquid detergent which contains finely divided swelling bentonite as a fabric softening material.
• a number of suitable bentonite materials is suggested for use, including Wyoming bentonite.
• liquid detergent composition for washing fabrics and imparting softness thereto, the composition comprising
• a fabric softening clay material having a swellability in water (determined as herein described) of more than 36% and a swellability in an 8% sodium-tripolyphosphate solution of less than 25%.
• the fabric softening clay materials which are useful in the compositions are characterised by their swelling behaviour, which is quantified by the following test.
• Two dispersions are prepared at room temperature containing respectively:
• the dispersions are stirred for 5 minutes with a magnetic stirrer and then placed in a 1000 ml measuring cylinder. The dispersions are then left to stand, undisturbed for two weeks. After this time the dispersions are examined. Generally some separation will have occurred. A lower layer of dispersion or gel containing the clay will be visibly distinguishable from a relatively clear upper layer. The height of the lower layer (h) and the overall height of the total liquid (H) are determined and percentage swellability (S) is calculated using the expression
• clay materials having a swellability (S) of more than 36%, preferably more than about 75% in dispersion A, and less than 25%, preferably less than about 20% in dispersion B are useful in the present composition.
• the clay materials which are useful in the present invention are some lamella smectite clays containing exchangeable sodium and calcium cations. Clay materials which are free of these ions, such as acid activated clays, do not swell sufficiently in water and do not provide a fabric softening benefit. It will be appreciated that in a practical liquid detergent product, the exchangeable cationics of the clay will exchange with those of the electrolyte system of the product prior to its actual use in the wash process. The softening benefit will therefore relate to this exchanged form.
• the level of fabric softening clay material in the product is preferably at least 1% by weight, but not more than 10% by weight. A most preferred level is from 3% to 7% by weight.
• the detergent compositions of the present invention necessarily contain one or more detergent active materials.
• the detergent compounds may be selected from anionic, nonionic, zwitterionic and amphoteric synthetic detergent active materials. Many suitable detergent compounds are commercially available and are fully described in the literature, for example in "Surface Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
• 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.
• suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C--C.
• alpha-olefins C 8 -C 2Q
• olefin sulphonates which term is used to 5 describe the material made by reacting olefins, particularly C-t 0 ⁇ C 20 alpha-olefins, with SO- and then neutralising and hydrolysing the reaction product.
• the preferred anionic detergent compounds are sodium (C ⁇ .-C. alkyl benzene sulphonates and sodium (C..-C. alkyl 10 sulphates.
• Suitable nonionic detergent compounds which may be used include in particular the reaction products of compounds having a hydrophobic group and a reactive
• nonionic detergent compounds include long chain tertiary a ine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
• 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
• compositions based on the much more commonly used synthetic anionic and/or nonionic detergent compounds 35 amounts in compositions based on the much more commonly used synthetic anionic and/or nonionic detergent compounds.
• detergent active materials may be used.
• the detergent active material is soap
• this is preferably selected from alkali metal salts of fatty acids having 12 to 18 carbon atoms.
• fatty acids having 12 to 18 carbon atoms.
• Typical such fatty acids are oleic acid, ricinoleic acid, and fatty acids derived from castor oil, rapeseed oil, groundnut oil, coconut oil, palmkernel oil or mixtures thereof.
• the sodium or potassium salts of these acids can be used.
• the level of detergent active material in the product is preferably at least 2% by weight, but not more than 45% by weight, most preferably from 6% to 15% by weight.
• the products according to the invention necessarily contain a detergency builder material to reduce the level of free calcium ions in the wash liquor and thereby improve detergency.
• This material may be selected from precipitating detergency builder materials such as alkali metal carbonates and ortho-phosphates, ion-exchange builder materials such as alkali metal aluminosilicates and sequestering builder materials such as alkali metal tripolyphosphates, citrates and nitrilotriacetates. Particularly preferred is sodium tripolyphosphate for reasons of product structure and building efficiency. At least 5% by weight of the detergency builder material is required to provide a noticeable effect upon detergency.
• the product be in the form of a structured liquid, that is a liquid which - 9 -
• the level of detergency builder material in the product is more than would dissolve at 20°C. .
• a preferred level is from 22 to 35% by weight, based on the weight of the product.
• the liquid detergent composition of the invention may further contain any of the adjuncts normally used in fabric washing detergent compositions, eg sequestering agents such as ethylenedia ine tetraacetate; buffering agents such as alkali silicates; soil suspending and anti-redepositon agents such as sodium carboxymethyl cellulose and polyvinylpyrrolidone; fluorescent agents; perfumes; germicides; and colourants.
• sequestering agents such as ethylenedia ine tetraacetate
• buffering agents such as alkali silicates
• soil suspending and anti-redepositon agents such as sodium carboxymethyl cellulose and polyvinylpyrrolidone
• fluorescent agents such as sodium carboxymethyl cellulose and polyvinylpyrrolidone
• perfumes germicides
• colourants eg.g sequestering agents such as ethylenedia ine tetraacetate
• buffering agents such as alkali silicates
• lather depressors such as silicones, and enzymes, particularly proteolytic and amylolytic enzymes
• peroxygen bleaches such as sodium perborate and potassium dichlorocyanurate
• bleach activators such as N,N,N',N',- tetraacetyl ethylene dia ine
• agents for improving the thermal stability of the product such as sodium toluene sulphonate, xylene sulphonate.or cumene sulphonate, at levels of up to 1% by weight, such as from 0.4% to 0.5%.
• the products of the present invention may be prepared by a variety of methods. However, we have found that benefits arise from mixing ingredients in a particular order. Thus, it is preferable to add a portion of the detergency builder to water, before adding the clay and the detergent active material. In this way products having uniform rheological properties from batch to batch can be obtained.
• a preferred method is to add the necessary quantity of water at an elevated temperature of say 40°C-80°C to a mixing vessel provided with a stirrer. An amount of between one part in twenty and one part in four of the detergency builder is then added, with stirring.
• the detergency builder is water-soluble, this amount will dissolve in the water and prevent the clay material from swelling but will not be sufficient to impair the stability of the surfactant.
• the clay material is then added and dispersed with stirring.
• the remaining part of the detergency builder is then added while maintaining this elevated temperature with stirring until a homogeneous mass is obtained.
• the clay When, alternatively, the clay is added to the water before any detergency builder, the clay swells producing a composition which may have a viscosity which is higher than desired. If all the detergency builder is added before the clay a product may result which separates on standing. If both the detergent active material and the detergency builder are added before the clay, the product may already have a high viscosity so that the powdered clay cannot easily be added without at the same time introducing air into the product resulting in a product having a density lower than may be desired.
• compositions of the invention should have a viscosity of less than 3000, preferably less than 1500 cPs measured at 20°C and at a shear rate of 21 sec . Most preferably the viscosity is between 650 and 850 cPs. Viscosities below 650 cPs can result in a loss of product stability.
• a liquid detergent composition was prepared according to the following formulation: Ingredient % (by weight)
• SCMC Sodium carboxymethyl cellulose
• composition was made by the following method:
• the water is heated to 60°C and maintained at that temperature.
• 2% STP is added, followed by the clay, SCMC, fluorescer, sodium hydroxide, silicate, glycerol, borax, fatty acid and sulphonic acid (which with the sodium hydroxide generate the soap and the anionic detergent active respectively) and nonionic active while stirring is continued. After 10 minutes agitation the remaining 20.8% STP was added and the mixture was then cooled with further stirring. When cool, the silicone, perfume and enzymes were added.
• compositions were prepared containing different clay materials. In each case the product viscosity was measured at 20°C and 21 sec " . Each composition was used to wash cotton test cloths using the following wash metho :
• Cotton terry towelling test cloths which have been preharshened by 10 washes in a commercially available fabric washing powder product SKIP (ex Lever, France) , are washed in the test product for 20 minutes at 40°C using tap water with a hardness of 48°FH.
• a laboratory scale apparatus having a capacity of 1 litre is used, and three test cloths of size 15cm x 15cm are washed together. After washing, the cloths are rinsed twice in tap water, wrung out and line dried for 24 hours.
• a mixture of fabric test cloths were washed with detergent compositions as set out below at 40°C in water having a hardness of 30°FH (3 x 10 ⁇ molar free calcium ions) .
• Some test cloths consisted of new terry towelling, some consisted of new acrylic fibres and a third group consisted of terry towelling pieces which had been pre-harshened by washing 30 times in a commercially available softener-free powder product SKIP (ex Lever, France) in 45°FH water.
• Formulation 2WB is substantially identical to Example 1, utilises STEETLEY NO 1 White Bentonite as the clay component.
• Formulation 2W is identical except that the clay component has been omitted.
• Formulations 2P and 2L are intended to represent commercially available fabric washing products used at recommended dosages for those products. As will be seen from the softening results, formulation 2WB is preferred to all other formulations tested.

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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)
• Chemical Or Physical Treatment Of Fibers (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

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Citations (2)

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• 1985
  • 1985-11-22 GB GB858528798A patent/GB8528798D0/en active Pending
• 1986
  • 1986-11-18 AU AU65349/86A patent/AU576100B2/en not_active Expired
  • 1986-11-19 KR KR1019860009779A patent/KR900008341B1/ko not_active Expired
  • 1986-11-19 CA CA000523339A patent/CA1335778C/en not_active Expired - Lifetime
  • 1986-11-20 ZA ZA868805A patent/ZA868805B/xx unknown
  • 1986-11-21 EP EP88119284A patent/EP0317926B1/en not_active Expired - Lifetime
  • 1986-11-21 JP JP61278527A patent/JPS62129391A/ja active Granted
  • 1986-11-21 EP EP86309135A patent/EP0225142B1/en not_active Expired
  • 1986-11-21 DE DE8888119284T patent/DE3688082T2/de not_active Expired - Lifetime
  • 1986-11-21 ES ES86309135T patent/ES2011016B3/es not_active Expired
  • 1986-11-21 ES ES88119284T patent/ES2053687T3/es not_active Expired - Lifetime
  • 1986-11-21 WO PCT/GB1986/000712 patent/WO1987003297A1/en not_active Ceased
  • 1986-11-21 DE DE8686309135T patent/DE3665882D1/de not_active Expired
  • 1986-12-11 BR BR8606161A patent/BR8606161A/pt not_active IP Right Cessation
• 1989
  • 1989-04-13 US US07/338,499 patent/US5017296A/en not_active Expired - Lifetime

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