Detergent compositions.
Abstract
Detergent compositions contain a combination of surfactants exhibiting enhanced detergency: an alkylpolyglycoside, preferably having a degree of polymerisation of 1 to 1.8, together with a nonionic surfactant chosen from glyceryl ethers and esters, esters of reducing saccharides, and aliphatic alcohols. Aqueous liquid detergent compositions also exhibit improved stability.

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15 claims: 4 independent, 11 dependent
- 11 A detergent composition containing (i) an alkylpolyglycoside of the general formula RO(R′O) t (G) x in which R is an organic hydrophobic resisue containing 10 to 20 carbon atoms, R′ contains 2 to 4 carbon atoms, G is a saccharide residue containing 5 or 6 carbon atoms, t is in the range 0 to 25 and x is in the range from 1 to 10; and (ii) a nonionic surfactant, characterised in that the nonionic surfactant (ii) is chosen from:(a) ethers and esters of the respective formulae wherein R³ is an organic hydrophobic residue having from 7 to 20 carbon atoms and denotes part of a polyhydric alcohol whose formula is HOZ and which has 2 to 4 carbon atoms, (b) C₈ to C₂₀ estere of reducing saccharides containing 5 or 6 carbon atoms, (c) aliphatic alcohols of 6 to 20 carbon atoms, and mixtures of any of these surfactants.
- 77 A detergent composition according to any one of the preceding claims, characterised in that the nonionic surfactant (ii) (a) is a monoglyceryl ether or ester of respective formulae
- 1010 A composition according to claim 10, characterised in that the ester is 6-0-alkanoyl glucoside.
- 1212 A detergent composition according to any one of the preceding claims, characterised in that it comprises 1 to 60% by weight of a surfactant mixture which contains the said alkylpolyglycoside (i) and the said nonionic surfactant (ii) in amounts which total 75 to 100% by weight of the surfactant mixture, the composition also containing other ingredients and/or water.
- 1515 A method of cleaning characterised in that it comprises contacting fabrics or other inanimate surface to be cleaned with a composition according to any one of the preceding claims, or a wash liquor comprising water and a composition according to any one of the preceding claims, added to the water in a quantity lying in a range from 0.5 to 50 grams per litre of water.
Independent claims6
106 paragraphs in 1 section, as filed
Field of the Invention
0001This invention relates to detergent compositions, particularly but not exclusively to built detergent compositions for washing fabrics.
Background of the Invention
0002Detergent compositions traditionally contain one of more detergent active materials in addition to various other ingredients such as detergency builders, bleaches, flourescers, perfumes etc. Notable applications of detergent compositions are to clean fabrics, usually by washing portable fabric items in a bowl or in a washing machine, to clean crockery and cooking utensils, again by washing in a bowl (hand dishwashing), and to clean hard surfaces such as glass, glazed surfaces, plastics, metals and enamels. A number of classes of surfactant materials have been used as detergent active materials, including anionic and nonionic materials.
0003One known category of nonionic surfactants are compounds which are often known as alkylpolyglycosides. These are of the general formula<maths id="math0001" num="(I)"><math display="block"><mrow><msub><mrow><mtext>RO (R′O)</mtext></mrow><mrow><mtext>t</mtext></mrow></msub><msub><mrow><mtext> (G)</mtext></mrow><mrow><mtext>x</mtext></mrow></msub></mrow></math><img file="EP0487262A2_D0001.tif" /></maths> in which R is an organic hydrophobic residue, R′O is an alkoxy group which may be absent because t can be zero, and G is a saccharide residue and x is at least unity. A more detailed definition is set out hereinafter.
0004We have now found that a combination of alkylpolyglycoside with certain unethoxylated nonionic surfactants provides unexpected advantages. Such combinations have been found to give a synergistic benefit of enhanced oily/fatty soil detergency. Furthermore, such combinations have been found to provide stable structured liquid detergent compositions containing significant levels of nonionic surfactant. By eliminating ethylene oxide groups from the nonionic surfactant, aquatic toxicity is reduced and the possibility of carcinogenic contamination removed.
0005EP 75 995A and EP 75 996A (Procter & Gamble) disclose alkylpolyglycosides in combination with various nonionic surfactants. Among the numerous classes of nonionic cosurfactants disclosed are glyceryl ethers of the general formula <chemistry id="chem0001" num="0001"><img file="EP0487262A2_D0002.tif" /></chemistry> wherein R⁹ is a C₈₋₁₈ alkyl or alkenyl group or a C₅₋₁₄ alkaryl group and n is from 0 to 6; but conventional ethoxylated alcohol nonionic surfactants are preferred and specifically exemplified.
Definition of the invention
0006According to the present invention there is provided a detergent composition containing <ul id="ul0001" list-style="none"><li>(i) an alkylpolyglycoside of the general formula<maths id="math0002" num=""><math display="block"><mrow><msub><mrow><mtext>RO(R′O)</mtext></mrow><mrow><mtext>t</mtext></mrow></msub><msub><mrow><mtext> (G)</mtext></mrow><mrow><mtext>x</mtext></mrow></msub></mrow></math><img file="EP0487262A2_D0003.tif" /></maths> in which R is an organic hydrophobic residue containing 10 to 20 carbon atoms, R′ contains 2 to 4 carbon atoms, G is a saccharide residue containing 5 or 6 carbon atoms, t is in the range 0 to 25 and x is in the range from 1 to 10;</li><li>(ii) a nonionic surfactant which is chosen from <ul id="ul0002" list-style="none"><li>(a) ethers and esters of the respective formulae <chemistry id="chem0002" num="0002"><img file="EP0487262A2_D0004.tif" /></chemistry> wherein R³ is an organic hydrophobic residue having from 7 to 20 carbon atoms and denotes part of a polyhydric alcohol whose formula is HOZ and which has 2 to 4 carbon atoms,</li><li>(b) C₈ to C₂₀ esters of reducing saccharides containing 5 or 6 carbon atoms,</li><li>(c) aliphatic alcohols of 6 to 20 carbon atoms, and mixtures of any of these surfactants. </li></ul></li></ul>
0007The weight ratio of the alkyl polyglycoside and the other specified surfactant(s) will generally lie within a range of 20:1 to 1:20 and may lie in a narrower range from 9:1 to 1:9 or even 4:1 to 1:4. The preferred ratio of the surfactants will depend on the specific surfactants and the nature of the product.
0008For structured liquids it will generally be desirable to achieve both good stability and good but not necessarily optimum detergency. For particulate compositions it may be possible to optimise detergency.
0009The weight ratio range which gives synergy will vary depending on the specific surfactants used and can be determined by experiment.
0010The invention also provides a method of washing which comprises contacting fabrics, or an inanimate surface to be cleaned, with a composition according to this invention or a wash liquor obtainable by adding the composition to water, notably in an amount ranging from 0.5 to 50 grams of composition per litre of water.
The alkylpolyglycoside (i)
0011In the general formula<maths id="math0003" num=""><math display="block"><mrow><msub><mrow><mtext>RO(R′O)</mtext></mrow><mrow><mtext>t</mtext></mrow></msub><msub><mrow><mtext> (G)</mtext></mrow><mrow><mtext>x</mtext></mrow></msub></mrow></math><img file="EP0487262A2_D0005.tif" /></maths> the hydrophobic group R is preferably aliphatic, either saturated or unsaturated, notably straight or branched alkyl, alkenyl, hydroxyalkyl or hydroxyalkenyl. However, it may include an aryl group for example alkyl-aryl, alkenyl-aryl and hydroxyalkyl-aryl. Particularly preferred is that R is alkyl or alkenyl of 8 to 16 carbon atoms.
0012The value of t in the general formula above is preferably zero, so that the -(RO)<sub>t</sub>- unit of the general formula is absent. In that case the general formula becomes<maths id="math0004" num="(II)"><math display="block"><mrow><msub><mrow><mtext>RO(G)</mtext></mrow><mrow><mtext>x</mtext></mrow></msub></mrow></math><img file="EP0487262A2_D0006.tif" /></maths>
0013If t is non-zero it is preferred that R′O is an ethylene oxide residue. Other likely possibilities are propylene oxide and glycerol residues. If the parameter t is non-zero so that R′O is present, the value of t (which may be an average value) will preferably lie in the range from 0.5 to 10.
0014The group G is typically derived from fructose, glucose, mannose, galactose, talose, gulose, allose, altrose, idose, arabinose, xylose, lyxose and/or ribose. Preferably, the G is provided substantially exclusively by glucose units.
0015The value x, which is an average, is usually termed the degree of polymerisation. Desirably x varies between 1 and 8. Values of x may lie between 1 and 3, especially 1 and 1.8.
0016Polyglycosides of particular interest have x in the narrow range from 1 or 1.2 up to 1.4 or especially 1.3. If x exceeds 1.3 it preferably lies in the range 1.3 or 1.4 to 1.8.
0017When x lies in the range 1 to 1.4 it is preferred that R is C₈ to C₁₄ alkyl or alkenyl. The even narrower range of C₈ to C₁₂ may be used.
The nonionic surfactant (ii)
0018These specified nonionic surfactants are generally hydrophobic in character. This is manifested by formation of a turbid dispersion rather than an isotropic solution when placed, alone, in deionised water at a surfactant concentration of 1% or more by weight.
0019A first possible class of cosurfactants is comprised by monoglyceryl ethers or esters with the respective formulae <chemistry id="chem0003" num="0003"><img file="EP0487262A2_D0007.tif" /></chemistry> in which R³ is as specified previously, i.e. an organic hydrophobic residue of 7 to 20 carbon atoms. R³ is preferably a saturated or unsaturated aliphatic residue. In particular R³ may be linear or branched alkyl or alkenyl. More preferably, R³ is a substantially linear alkyl or alkenyl moiety having from 8 to 16 carbon atoms, notably a C₈-C₁₂ alkyl moiety. Moat preferably, R³ is decyl, undecyl or dodecyl.
0020The monoglyceryl ethers of alkanols are known materials and can be prepared, for example, by the condensation of a higher alkanol with glycidol. Glycerol monoesters are of course well known and available from various suppliers including Alkyril Chemicals Inc.
0021Another possibility for the nonionic surfactant (ii) is comprised by C₇ to C₂₀ acyl mono and di esters of C₂-C₄ polyhydric alcohols other than glycerol which has already been mentioned. C₇ to C₂₀ ethers of such alcohols are also possible.
0022Yet another possibility is C₆ to C₂₀ aliphatic alcohol. Preferably such alcohol has 10 to 18 carbon atoms.
0023As also mentioned above, yet another possibility is a C₈ to C₂₀ ester of a reducing hexose or pentose sugar. Such a compound is also referred to as an 0-alkanoyl derivative of the sugar.
0024O-alkanoyl glucosides are described in WO 88/10147A (Novo Industri A/S). In particular the surfactants described therein are glucose esters with the acyl group attached in the 3- or 6- position such as 3-0-acyl-D-glucose or 6-0-acyl-D-glucose. In the present invention we prefer to use a 6-0-alkanoyl glucoside, especially compounds having the formula: <chemistry id="chem0004" num="0004"><img file="EP0487262A2_D0008.tif" /></chemistry> wherein R⁵ is an alkyl or alkenyl group having from 7 to 19 preferably 11 to 19 carbon atoms, and R⁶ is hydrogen or an alkyl group having from 1 to 4 carbon atoms.
0025Most preferred are such compounds where R⁶ is an alkyl group, such as ethyl or isopropyl. Alkylation in the 1- position enables such compounds to be prepared by regiospecific enzymatic synthesis as described by Bjorkling et al. (J. Chem. Soc., Chem. Commum. 1989 p934) the disclosure of which is incorporated herein by reference.
0026While the above description concerns surfactants based on glucose, it is envisaged that corresponding materials based on other reducing sugars, such as galactose and mannose are also suitable.
Further surfactants
0027Detergent compositions of the invention may contain further surfactants, outside the definitions stated for (i) and (ii). The amount of any additional surfactant will frequently be less than 50% by weight, and perhaps less than 25% or even 10% by weight of the overall surfactant mixture.
0028Additional surfactant, if present, may be anionic, nonionic or amphoteric. Cationic surfactant is possible if anionic surfactant is absent. In particular, nonionic surfactant with an HLB value greater than 10.5 may be present. This may for instance be ethoxylated fatty alcohol.
0029Compositions of this invention will generally contain a surfactant mixture comprising (i) the specified alkylpolyglycoside (ii) the specified nonionic surfactant and (iii) any other surfactant(s), in a total amount which is from 1 to 60% by weight of the composition.
0030Preferred amounts are 2 to 45%, better 5 to 40% or 35%. The amount of the specified surfactants (i) and (ii) may itself be at least 2% or at least 5% of the overall composition.
Other ingredients
0031The compositions of the invention may contain an electrolyte, for instance present in such an amount to give a concentration of at least 0.01 molar, when the composition is added to water at a concentration of 1 g/litre. Electrolyte concentration may possibly be higher such as at least 0.05 or 0.1 molar especially if the composition is of solid form: liquid compositions generally limit electrolyte for the sake of stability. 1 g/litre is approximately the lowest level at which detergent compositions for fabric washing are used in usual practice. More usual is usage at a level of 4 to 50 g/litre. The amount of electrolyte may be such as to achieve an electrolyte concentration of 0.01 molar, most preferably at least 0.1 molar, when the composition is added to water at a concentration of 4 g/litre.
0032If the composition of the invention is intended as a fabric washing composition it will generally contain detergency builder in an amount from 7 to 70% by weight of the composition.
0033If it is in solid form, the composition is likely to contain at least 10 or 15% of builder.
0034It is desirable that the compositions according to the invention be approximately neutral or at least slightly alkaline, that is when the composition is dissolved in an amount to give surfactant concentration of 1 g/l in distilled water at 25°C the pH should desirably be at least 7.5. For solid compositions the pH will usually be greater, such as at least 9. To achieve the required pH, the compositions may include a water-soluble alkaline salt. This salt may be a detergency builder (as described in more detail below) or a non-building alkaline material.
0035When the compositions of the invention contain a detergency builder material, this may be any material capable of reducing the level of free calcium ions in the wash liquor and will preferably provide the compositions with other beneficial properties such as the generation of an alkaline pH and the suspension of soil removed from the fabric.
0036Examples of phosphorus-containing inorganic detergency builders, when present, include the water-soluble salts, especially alkali metal pyrophosphates, orthophosphates, polyphosphates and phosphonates. Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, ortho phosphates and hexametaphosphates.
0037Examples of non-phosphorus-containing inorganic detergency builders, when present, include water-soluble alkali metal carbonates, bicarbonates, silicates and crystalline and amorphous alumino silicates. Specific examples include sodium carbonate (with or without calcite seeds), potassium carbonate (with or without calcite seeds), sodium and potassium bicarbonates and silicates.
0038Examples of organic detergency builders, when present include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetyl carboxylates and polyhydroxysulphonates. Specific examples include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acids and citric acid. Further possibilities are tartrate monosuccinates, tartrate disuccinates, dipicolinic acid, cheledamic acid, carboxymethyloxysuccinate and hydroxyethyl imino diacetic acid.
0039Examples of other optional ingredients which may be present in the composition are polymers containing carboxylic or sulphonic acid groups in acid form or wholly or partially neutralised to sodium or potassium salts, the sodium salts being preferred. Preferred polymers are homopolymers and copolymers of acrylic acid and/or maleic acid or maleic anhydride. Of especial iterest are polyacrylates, polyalphahydroxyacrylates, acrylic/maleic acid copolymers, and acrylic phosphinates. Other polymers which are especially preferred for use in liquid detergent compositions are deflocculating polymers such as for example disclosed in EP 346 995A (Unilever).
0040The molecular weights of homopolymers and copolymers are generally 1000 to 150 000, preferably 1500 to 100 000. The amount of any polymer may lie in the range from 0.5 to 5% by weight of the composition. Other suitable polymeric materials are cellulose ethers such as carboxy methyl cellulose, methyl cellulose, hydroxy alkyl celluloses, and mixed ethers, such as methyl hydroxy ethyl cellulose, methyl hydroxy propyl cellulose, and methyl carboxy methyl cellulose. Mixtures of different cellulose ethers, particularly mixtures of carboxy methyl cellulose and methyl cellulose, are suitable.
0041Polyethylene glycol of molecular weight from 400 to 50 000, preferably from 1000 to 10 000, and copolymers of polyethylene oxide with polypropylene oxide are suitable as also are copolymers of polyacrylate with polyethylene glycol. Polyvinyl pyrrolidone of molecular weight of 10 000 to 60 000 preferably of 30 000 to 50 000 and copolymers of polyvinyl pyrrolidone with other poly pyrrolidones are suitable. Polyacrylic phosphinates and related copolymers of molecular weight 1000 to 100 000, in particular 3000 to 30 000 are also suitable.
0042Further examples of other ingredients which may be present in the composition include fabric softening agents such as fatty amines, fabric softening clay materials, 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, typically accompanied by peracid bleach precursors, organic peracids, chlorine-releasing bleaching agents such as trichloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually present in very minor amounts, fluorescent agents, perfumes including deodorant perfumes, enzymes such as cellulases, proteases, lipases and amylases, germicides and colourants.
Product forms
0043The detergent compositions according to the invention may be in any suitable form including powders, bars, liquids and pastes. For example suitable liquid compositions may be non-aqueous or aqueous, the latter being either isotropic or lamellar structured. The compositions may be prepared by a number of different methods according to their physical form. In the case of granular products they may be prepared by dry-mixing, coagglomeration, spray-drying from an aqueous slurry or any combination of these methods.
0044One preferred physical form is a granule incorporating a detergency builder salt. This may be prepared by conventional granulation techniques or spray drying.
0045Another preferred physical form is a lamellar structured aqueous liquid. Structuring a liquid by means of surfactant is well known and may be utilised to provide consumer-preferred flow properties, and/or turbid appearance. Also many liquids in which the surfactant mixture provides structure are capable of suspending particulate solids such as detergency builders and abrasives. For such forms, alkyl polyglycosides which are particularly suitable have a HLB of at least 12.0 and in the formula<maths id="math0005" num=""><math display="block"><mrow><msub><mrow><mtext>RO (R′O)</mtext></mrow><mrow><mtext>t</mtext></mrow></msub><msub><mrow><mtext>(G)</mtext></mrow><mrow><mtext>x</mtext></mrow></msub></mrow></math><img file="EP0487262A2_D0009.tif" /></maths> t is zero or 1 to 3, preferably zero, while x is 1 to 3, especially 1 to 1.8.
0046The aqueous continuous phase will usually contain some dissolved electrolyte. Electrolyte may be dissolved only in the aqueous continuous phase or may also be present as suspended solid particles. Particles of solid materials which are insoluble in the aqueous phase may be suspended alternatively or in addition to any solid electrolyte particles.
0047Although structured liquids require some electrolyte to be present in the continuous phase, the amount which is present generally has to be limited for the sake of stability. When the present invention takes the form of a structured liquid, an advantage is that the structuring conferred by the surfactant mixture of the invention will tolerate a substantial amount of electrolyte.
0048Three common product forms which are of the structured liquid types are liquids for heavy duty fabrics washing, liquid abrasives and general purpose cleaners.
0049In the first class, the suspended solid can comprise suspended solids which are substantially the same as the dissolved electrolyte, being an excess of same beyond the solubility limit. This solid is usually present as a detergency builder, i.e. to counteract the effects of calcium ion water hardness in the wash.
0050In the second class, the suspended solid usually comprises a particulate abrasive, insoluble in the system. In that case the electrolyte, present to contribute to the structuring of the active material in the dispersed phase, is generally different from the abrasive compounds. In certain cases, the abrasive can however comprise partially soluble salts which dissolve when the product is diluted.
0051In the third class, the structure is usually used for thickening the product to give consumer- preferred flow properties, and sometimes to suspend pigment particles.
0052The invention will now be further illustrated by the following non-limiting Examples, in which parts and percentages are by weight unless otherwise stated.
EXAMPLES
Example 1
0053Aqueous wash liquors were prepared containing the following materials in deionised water. <tables id="tabl0001" num="0001"><img file="EP0487262A2_D0010.tif" /></tables>
0054These quantities would be typical of using 6 g/litre of a particulate detergent product containing 16.7 % by weight surfactant. The wash liquors had pH of about 10, resulting from the presence of the metaborate.
0055The alkylpolyglycoside was APG 300 from Horizon Chemical Co. This was of the formula<maths id="math0006" num=""><math display="block"><mrow><msub><mrow><mtext>RO(G)</mtext></mrow><mrow><mtext>x</mtext></mrow></msub></mrow></math><img file="EP0487262A2_D0011.tif" /></maths> where R is a 9 to 11 carbon alkyl chain, G is glucose and x has an average value of 1.4.
0056The decyl monoglyceryl ether was from Unichema. Its formula was <chemistry id="chem0005" num="0005"><img file="EP0487262A2_D0012.tif" /></chemistry> where R³ was C₁₀ alkyl.
0057Wash liquors were prepared with various ratios of the two surfactants and used to wash polyester test cloths soiled with radiolabelled triolein. Washing was carried out at 40°C for 20 minutes in a Tergotometer.
0058The removal of triolein was determined and the results are set out in Table 1 below.
Example 2
0059Example 1 was repeated, using 1-O-ethyl 6-0-dodecanoylglucoside (from Novo Industri) as the hydrophobic nonionic surfactant. Such a material conforms to the general formula (A) above with R⁵ = C₁₂ alkyl and R⁶ = ethyl. Again results are included in Table 1.
Examples 3 and 4
0060Examples 1 and 2 were repeated using a different alkylpolyglycoside. APG 500 from Horizon was used. This has the formula<maths id="math0007" num=""><math display="block"><mrow><msub><mrow><mtext>R (G) </mtext></mrow><mrow><mtext>x</mtext></mrow></msub></mrow></math><img file="EP0487262A2_D0013.tif" /></maths> where R is C₁₂ and C₁₃ alkyl, G is glucose and x is 1.4.
0061Results are set out in Table 2 below. <tables id="tabl0002" num="0002"><img file="EP0487262A2_D0014.tif" /></tables><tables id="tabl0003" num="0003"><img file="EP0487262A2_D0015.tif" /></tables>
0062It can be seen from the tables that in every example there is a mixture of surfactants which gives better triolein removal than either individual surfactant. The proportions giving synergy depended on the nature of the surfactants and can be found by experiments such as these.
Examples 5 to 7
0063Structured liquid compositions were prepared with the formulations given below. In each case the formulations were prepared by mixing the nonionic surfactants together and then dispersing this premix into a mixture of water and the other ingredients.
0064The alkylpolyglycoside was APG 600 from Horizon which has the formula<maths id="math0008" num=""><math display="block"><mrow><msub><mrow><mtext>RO(G)</mtext></mrow><mrow><mtext>x</mtext></mrow></msub></mrow></math><img file="EP0487262A2_D0016.tif" /></maths> where R is derived from coconut, and is C₁₂ to C₁₆, predominantly C₁₂ and C₁₄, G is glucose and x has an average value of 1.4.
0065The monoglyceryl ester was the same as used in Example 1.
0066Synperonic A7 is C₁₃-C₁₅ alcohol ethoxylated with an average of 7 ethylene oxide residues. HLB value is 11.7.
0067The formulations were: <tables id="tabl0004" num="0004"><img file="EP0487262A2_D0017.tif" /></tables>
0068The compositions were stable and showed no phase separation on storage for at least one week at ambient temperatures.
0069The pH of the compositions was approximately 7.5.
Example 8
0070A structured liquid composition was prepared by adding the ingredients in the following order: Water, fluorescer, zeolite, APG (as 50% active material in water), citrate, citric acid, glycerol, borax, a premix of Synperonic A7 and the glyceryl ether, then remaining ingredients. The formulation was: <tables id="tabl0005" num="0005"><img file="EP0487262A2_D0018.tif" /></tables>
0071The glyceryl ether was the same material as used in Examples 1 and 5.
0072Narlex LD31 is a polyacrylate having a molecular weight of about 4000, ex National Starch; DB 100 is a silicone antifoam material ex Dow Corning.
0073Tinopal CBS-X is a fluorescer material.
0074The composition did not show any phase separation upon storage for 2 months at ambient temperature, the viscosity of the product was 830 mPas at 21 s⁻¹, the pH of the product was 8.1.
Examples 9 and 10
0075Two suitable formulations for a granular detergent composition are as follows: <tables id="tabl0006" num="0006"><img file="EP0487262A2_D0019.tif" /></tables>
0076The granular compositions may be prepared by agglomeration of the ingredients into granules using a pan granulator, or can be produced by conventional spray drying and post dosing.
Example 11, Comparative Example A
0077Wash liquors were prepared containing 5 g/l each of the formulations given below, typical of granular detergent compositions free of sodium sulphate, in 24°FH water. Radio-labelled triolein removal was monitored in a 20-minute wash at 40°C as described in Example 1. <tables id="tabl0007" num="0007"><img file="EP0487262A2_D0020.tif" /></tables>
0078The glyceryl ether was the same material as used in Example 1.
0079The APG 600 was a similar material to that used in Example 5, but obtained from Henkel Chemical Company.
0080Sokalan (Trade Mark) CP5 is an acrylic/maleic copolymer ex BASF.
0081The system containing the low-HLB cosurfactant clearly gave the better cleaning.
Example 12, Comparative Example B
0082The procedure of Examples 11 and A was repeated using wash liquors containing the formulations given below, containing sodium sulphate and a lower surfactant level, at concentrations of 6 g/l. <tables id="tabl0008" num="0008"><img file="EP0487262A2_D0021.tif" /></tables>
0083Again, the system containing the low-HLB cosurfactant gave the better cleaning.
Example 13, Comparative Examples C to E
0084In this Example, the combination of APG 600 (as used in Examples 11 and 12) with C₁₀ monoglyceryl ether was compared with combinations of APG 600 with ethoxylated C₁₀ monoglyceryl ethers. The methodology was as in Example 1, the surfactant systems being dissolved to a total concentration of 1 g/l in 0.05M sodium metaborate at 40°C in demineralised water.
0085The cosurfactants used were as follows: <dl id="dl0001"><dt>Example 13:</dt><dd>C₁₀ glyceryl monoether (as Example 1)</dd><dt>Example C:</dt><dd>C₁₀ (EO)₂ glyceryl monoether</dd><dt>Example D:</dt><dd>C₁₀ (EO)₄ glyceryl monoether</dd><dt>Example E:</dt><dd>C₁₀ (EO)₆ glyceryl monoether</dd></dl>
0086The results are shown in Table 3, where the asterisked figures represent the highest detergency attained with each combination. <tables id="tabl0009" num="0009"><img file="EP0487262A2_D0022.tif" /></tables>
0087Alone, all the ethoxylated glyceryl ethers were clearly better surfactants than the unethoxylated material, the 2EO glyceryl ether being the best and detergency then deteriorating with increasing degree of ethoxylation; the 2EO and 4EO materials being superior to APG 600 alone, while the 6EO material was inferior.
0088As expected, combination of APG 600 with the 2EO material gave no advantage but simply reduced the detergency towards the lower value shown by the APG alone. With the 4EO material, a small synergistic benefit was found but the effect of the cosurfactant clearly predominated, the maximum detergency being observed at 20% APG/80% cosurfactant and being only slightly higher than that of the cosurfactant alone. With the 6EO material, the converse was true: a very small synergistic effect was possibly present but the effect of the APG clearly predominated, the maximum detergency being observed at 80% APG/20% cosurfactant and being only slightly higher than that of the APG alone.
0089The unethoxylated material, however, which on its own showed very poor detergency, exhibited very strong synergy with the APG and the maximum detergency, at 60% APG/40% cosurfactant, was substantially higher than that of the APG alone and only slightly lower than that obtained from the combination of APG with the much more efficient 4EO material.
28 sheets
Sheet 1 Sheet 2 Sheet 3 Sheet 4 Sheet 5 Sheet 6 Sheet 7 Sheet 8 Sheet 9 Sheet 10 Sheet 11 Sheet 12 Sheet 13 Sheet 14 Sheet 15 Sheet 16 Sheet 17 Sheet 18 Sheet 19 Sheet 20 Sheet 21 Sheet 22 Sheet 23 Sheet 24 Sheet 25 Sheet 26 Sheet 27 Sheet 28
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| WO9403569A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| CN1329018C | Cited by | China | Search report |
| WO0049873A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| WO2010076595A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| DE19926526A1 | Cited by | Germany | Search report |
| US7985773B2 | Cited by | United States of America | Applicant |
| WO9302171A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| EP1013754A1 | Cited by | European Patent Office (EPO) | Search report |
| US6849577B1 | Cited by | United States of America | Applicant |
| WO9302171A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| US6221816B1 | Cited by | United States of America | Applicant |
| AU755029B2 | Cited by | Australia | Search report |
| US5776882A | Cited by | United States of America | Search report |
| WO9814544A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| EP0075995A2 | Cites | European Patent Office (EPO) | Search report |
| EP0346995A2 | Cites | European Patent Office (EPO) | Search report |
| EP0380437A2 | Cites | European Patent Office (EPO) | Search report |
| EP0388810B1 | Cites | European Patent Office (EPO) | Search report |
| EP0423968A1 | Cites | European Patent Office (EPO) | Search report |
| US4627931A | Cites | United States of America | Search report |
17 members in 10 offices; this record represents the family
Priority claims3
| Document | Office | Kind | Date |
|---|---|---|---|
| 9025248 | United Kingdom | – | |
| 9025248 | United Kingdom | A | |
| GB19900025248 | – | – | – |
Members17
| Document | Office | Kind | |
|---|---|---|---|
| AU8793991A | Australia | A | |
| CA2055411A1 | Canada | A1 | |
| EP0487262A2This record | European Patent Office (EPO) | A2 | |
| KR920009965A | Republic of Korea | A | |
| JPH04292697A | Japan | A | |
| EP0487262A3 | European Patent Office (EPO) | A3 | |
| AU643849B2 | Australia | B2 | |
| TW231311B | Taiwan Province of China | B | |
| MY106915A | Malaysia | A | |
| KR950010007B1 | Republic of Korea | B1 | |
| JP2531553B2 | Japan | B2 | |
| CA2055411C | Canada | C | |
| EP0487262B1 | European Patent Office (EPO) | B1 | |
| DE69127955D1 | Germany | D1 | |
| ES2107443T3 | Spain | T3 | |
| IN173467B | India | B | |
| DE69127955T2 | Germany | T2 |
41 legal events, as 4 offices reported them to INPADOC
Over the term
Point at a mark for the eventEvents
| Event | Code | Office | |
|---|---|---|---|
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Announcement of lapse in spainLapsedFD2A | FD2A | ES | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Notification of lapseLapsedST | ST | FR | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Gb: european patent ceased through non-payment of renewal feeCeasedGBPC | GBPC | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| No opposition filedOpposition26N | 26N | EP | |
| No opposition filed within time limitOppositionORIGINAL CODE: 0009261PLBE | PLBE | EP | |
| Information on the status of an ep patent application or granted ep patentGrantedSTATUS: NO OPPOSITION FILED WITHIN TIME LIMITSTAA | STAA | EP | |
| Patent ceasedCeasedPL | PL | CH | |
| Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents actLapsedNLV1 | NLV1 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Fr: translation filedET | ET | EP | |
| It: translation for a ep patent filedITF | ITF | EP | |
| It: translation for a ep patent filedITF | ITF | EP | |
| Definitive protectionFG2A | FG2A | ES | |
| Corresponds to:REF | REF | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Designated contracting statesAK | AK | EP | |
| European patent takes effect as a national patent in ch/liEP | EP | CH | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| (expected) grantORIGINAL CODE: 0009210GRAA | GRAA | EP | |
| Despatch of communication of intention to grant a patentORIGINAL CODE: EPIDOS IGRAGRAH | GRAH | EP | |
| Despatch of communication of intention to grant a patentORIGINAL CODE: EPIDOS IGRAGRAH | GRAH | EP | |
| Despatch of communication of intention to grant a patentORIGINAL CODE: EPIDOS IGRAGRAH | GRAH | EP | |
| Despatch of communication of intention to grantORIGINAL CODE: EPIDOS AGRAGRAG | GRAG | EP | |
| First examination report despatched17Q | 17Q | EP | |
| Request for examination filed17P | 17P | EP | |
| Party data changed (applicant data changed or rights of an application transferred)RAP3 | RAP3 | EP | |
| Party data changed (applicant data changed or rights of an application transferred)RAP3 | RAP3 | EP | |
| Designated contracting statesAK | AK | EP | |
| Search report despatchedORIGINAL CODE: 0009013PUAL | PUAL | EP | |
| Designated contracting statesAK | AK | EP | |
| Public reference made under article 153(3) epc to a published international application that has entered the european phaseORIGINAL CODE: 0009012PUAI | PUAI | EP |
Numbers
- Publication
- 0487262
- Publication, DOCDB
- 0487262
- Publication, EPODOC
- EP0487262
- Application
- 913105615
- Application, DOCDB
- 91310561
- Application, EPODOC
- EP19910310561
Titles6
- German
- Detergenszusammensetzungen
- English
- Detergent compositions
- French
- Compositions détergentes
- German
- Detergenszusammensetzungen.
- English
- Detergent compositions.
- French
- Compositions détergentes.
Classification
- CPC, 5
- C11D1/825
- C11D1/662
- C11D1/72
- C11D1/74
- C11D17/0026
- IPC, 5
- C11D1 66
- C11D1 72
- C11D1 74
- C11D1 825
- C11D17 00
Designated states9
- Contracting states, 9
- Switzerland
- Germany
- Spain
- France
- United Kingdom
- Italy
- Liechtenstein
- Netherlands (Kingdom of the)
- Sweden