EP0328190A2 - Particulate laundry detergent composition - Google Patents
Particulate laundry detergent composition Download PDFInfo
- Publication number
- EP0328190A2 EP0328190A2 EP19890200221 EP89200221A EP0328190A2 EP 0328190 A2 EP0328190 A2 EP 0328190A2 EP 19890200221 EP19890200221 EP 19890200221 EP 89200221 A EP89200221 A EP 89200221A EP 0328190 A2 EP0328190 A2 EP 0328190A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- particulate
- mixture
- fatty acids
- laundry detergent
- mole
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 93
- 239000003599 detergent Substances 0.000 title claims abstract description 33
- 239000000344 soap Substances 0.000 claims abstract description 43
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 42
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 41
- 239000000194 fatty acid Substances 0.000 claims abstract description 41
- 229930195729 fatty acid Natural products 0.000 claims abstract description 41
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims abstract description 18
- 239000000843 powder Substances 0.000 claims abstract description 15
- 239000000463 material Substances 0.000 claims abstract description 14
- 229910000029 sodium carbonate Inorganic materials 0.000 claims abstract description 9
- 239000007787 solid Substances 0.000 claims abstract description 9
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims abstract description 6
- 239000011734 sodium Substances 0.000 claims abstract description 6
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 6
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims abstract 4
- 239000002253 acid Substances 0.000 claims description 20
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 12
- 235000003441 saturated fatty acids Nutrition 0.000 claims description 11
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 11
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 238000001816 cooling Methods 0.000 claims description 7
- 235000012149 noodles Nutrition 0.000 claims description 7
- 238000006386 neutralization reaction Methods 0.000 claims description 6
- 239000011236 particulate material Substances 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 4
- 238000002844 melting Methods 0.000 claims description 4
- 230000008018 melting Effects 0.000 claims description 4
- 239000007844 bleaching agent Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 102000004190 Enzymes Human genes 0.000 claims description 2
- 108090000790 Enzymes Proteins 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000011149 active material Substances 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- 230000003472 neutralizing effect Effects 0.000 claims 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 abstract description 6
- 239000004615 ingredient Substances 0.000 abstract description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract description 5
- 239000010452 phosphate Substances 0.000 abstract description 5
- 238000005406 washing Methods 0.000 abstract description 4
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 239000002245 particle Substances 0.000 description 9
- 239000010457 zeolite Substances 0.000 description 7
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 6
- 235000017550 sodium carbonate Nutrition 0.000 description 6
- 238000004090 dissolution Methods 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 150000004760 silicates Chemical class 0.000 description 5
- 238000012360 testing method Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 238000007580 dry-mixing Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 230000005496 eutectics Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- PMYUVOOOQDGQNW-UHFFFAOYSA-N hexasodium;trioxido(trioxidosilyloxy)silane Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])O[Si]([O-])([O-])[O-] PMYUVOOOQDGQNW-UHFFFAOYSA-N 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005649 metathesis reaction Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 238000010587 phase diagram Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- 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
- C11D9/06—Inorganic compounds
- C11D9/08—Water-soluble compounds
- C11D9/10—Salts
-
- 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
- C11D9/06—Inorganic compounds
- C11D9/08—Water-soluble compounds
- C11D9/10—Salts
- C11D9/12—Carbonates
-
- 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
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/26—Organic compounds, e.g. vitamins containing oxygen
- C11D9/267—Organic compounds, e.g. vitamins containing oxygen containing free fatty acids
-
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
-
- 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
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Definitions
- the present invention relates to a novel, particulate laundry detergent composition which contains no, or reduced levels of inorganic phosphate compounds. Furthermore, it relates to a particulate base material suitable for use in such detergent compositions and to a method of manufacturing this particulate base material.
- Conventional laundry detergent compositions contain phosphate compounds, especially sodium tripolyphosphate (STP), as building agents. Owing to the negative effects of phosphates on the environment, there has been an increasing interest in developing new laundry detergent compositions which have a low or zero phosphate content. However, it has proved to be difficult to match the excellent builder properties of the phosphate-containing compositions.
- STP sodium tripolyphosphate
- zeolites As builder in zero-P laundry detergent formulations.
- the application of zeolites in laundry detergent formulations has a number of drawbacks.
- zeolites In the first place, zeolites have a tendency to cause a bad powder structure. Further more, they tend to interact with silicates which are usually present in the composition as anti-corrosion agents, and they can cause dispensing problems in the washing machine and incrustation on the washed fabrics.
- compositions of the invention utilise acid soap both as a powder base and as a builder:
- the composition according to the invention comprises as a first particulate material a fatty acid mixture in which up to 35 mole% may be unsaturated fatty acids, which mixture has been neutralised to an extent of 25-60 mole %, and as a second particulate material a base in an amount sufficient to render the pH of the composition at a 0.5 wt% concentration in water higher than 8.
- detergent additives may be present, such as a bleach system, proteolytic enzymes, anti-foaming agents, optical brighteners, perfumes, anti-corrosion additives, etc.
- the composition according to the invention exhibits very satisfactory wash performance without the need for phosphate or zeolite builders, although the presence of low levels of these materials is not prohibited and may be beneficial. Powder properties such as flow and compressibility are also excellent.
- the particulate laundry detergent composition according to the invention preferably contains 30-80 wt.% of granular acid soap particles.
- the acid soap is a mixture of free fatty acids and soap, or a partially neutralized mixture of fatty acids.
- a wide range of saturated and/or unsaturated fatty acids may be used, but it was found that the powder properties of the particulate composition become less favourable at a content of unsaturated fatty acids of more than 35 mole%. More specifically, such powders tend to be sticky and are barely free-flowing.
- the mixture of fatty acid consists essentially of 5 - 20 mole% C16-C18 unsaturated fatty acids, and 95 - 80 mole% of a mixture of C8-C14 saturated fatty acids and C16-C18 saturated fatty acids in a ratio of 3:1-1:2.
- C8-C14 saturated fatty acids will also be referred to as laurics
- C14-C16 saturated fatty acids as stearics
- C16-C18 unsaturated fatty acids as oleics.
- the C16-C18 saturated fatty acids or stearics are mainly responsible for the builder properties, while they contribute little to detergency.
- the C16-C18 unsaturated fatty acids or oleics are important for their builder properties but especially for detergency.
- the C8-C14 saturated fatty acids or laurics contribute both to the building and to the detergency, but their main function is to facilitate processing of the soap/fatty acid mixture, and to ensure adequate dissolution properties.
- the laundry detergent compositions according to the present invention can be prepared by dry-mixing the various ingredients into a suitable mixture.
- the acid soap is used in the form of a particulate material, for example, prills or noodles.
- Particle size and shape may be chosen at will and are discussed in more detail below.
- These acid soap particles can be prepared by dissolving a suitable amount of soap in a mixture of fatty acid in the molten state, followed by solidification and processing of the solid mass. Alternatively, they can be prepared by partial in situ saponification or neutralization of a mixture of fatty acids. In this process, a solid base material is gradually admixed with the molten fatty acid mixture.
- Suitable basic compounds are, for example, soda ash (sodium carbonate), sodium disilicate or metasilicate, or sodium hydroxide.
- the operating temperature required to process these mixtures increases with the fatty acid chain length and degree of neutralization, and is preferably within the range of 70-140 C.
- the detergent composition of the present invention contains a particulate base in an amount sufficient to render the pH of the composition, at a 0.5 wt.% concentration in water, higher than 8.
- a base material in principle any base can be used which can be prepared in a particulate form and which readily dissolves in water without forming precipitates with the soap fatty acid particles.
- the same base is used as for the partial neutralization of the fatty acid mixture.
- the laundry detergent composition according to the invention may additionally contain other detergent compounds, such as anionic and/or nonionic non-soap detergent-active compounds. These may be incorporated in the particulate acid soap base, or present as a separate ingredient.
- the acid soap particles may contain up to 10% by weight of anionic and/or nonionic surfactant: higher levels can be detrimental to powder properties.
- anionic or nonionic surfactants may be carried on a porous inorganic material which is admixed with the acid soap particles.
- An example of such an adjunct is a liquid ethoxylated C13-C15 alcohol sprayed on to a Burkeite carrier. If the inorganic carrier is a basic material, the adjunct may serve as the basic component (second particulate material) of the composition.
- a particularly preferred method of preparing acid soap particles was found to be spray-cooling. It was found thereby that particles or prills are obtained with excellent properties with regard to the dissolution rate, stability and to wash performance of the complete detergent composition.
- prills of any desired size and bulk density can be obtained by manipulation of the process conditions. Prills of average particle size 250-1000 m and buk density 400-750 g/e are preferred for compatibility with the other solid ingredients of the compsition, so that segregation in the pack is minimised.
- soaps as well as fatty acids may form various eutectic complexes; such complexes may also be formed between soaps and fatty acids, resulting in highly' complicated phase diagrams for such mixtures.
- This aspect is particularly relevant to the question of meeting the 35-40 ° C target for the solidification temperature.
- the relative amounts of laurics and stearics should not exceed a 1:1 ratio; nevertheless, some liquefaction at the eutectic temperature of about 33 C cannot be avoided.
- the presence of some low melting laurics/stearics complex may be expected to have a favourable effect on the low temperature solubility.
- a number of fatty acid mixtures were prepared, having the compositions shown in Table A. The mixtures were then heated and at approximately 65. C they began to melt. Heating was continued and after complete melting at a temperature of about 80 C soda ash (sodium carbonate) was gradually added in an amount of 0.1 kg/min to control the C02-evolution until the desired degree of neutralization had been reached. At the same time, the temperature was gradually raised to approximately 140 ⁇ C.
- soda ash sodium carbonate
- the solubility was measured as follows: The rate of dissolution of the soap/fatty acid noodles was determined by monitoring the increase in conductivity resulting from dissolution of the soap part of the noodles. In this method, 3 g/I of the sample is added to 1 I demineralized water at 25 . C with continuous stirring, using a magnetic stirrer. The rate of dissolution is expressed as the time required to dissolve 50% of the soluble part of the soap/fatty acid blend (t1 ⁇ 2) . The maximum conductivity is measured after heating to above the melting temperature of the fatty acids, followed by cooling down to ambient temperature.
- Examples 1-3 were repeated, but instead the molten acid/soap mixtures were spray-cooled in a spray tower to form prills.
- the spray-cooling conditions are shown in Table B.
- the powder properties of the prills obtained are given in Table C.
- a mixture of fatty acids was prepared, having thefollowing composition :
- Example 7 The procedure of Example 7 was repeated, using a fatty acid mixture of the following composition :
- the acid soap prills obtained according to Example 7 were used to formulate a complete laundry detergent composition by dry-mixing various other ingredients to the prills, such as a nonionic detergent on a Burkeite carrier, a bleach system and an enzyme.
- composition of the complete detergent powder is given in Table E. Also shown are two commercially available laundry detergent compositions, composition B being a low-P and composition A a zero P composition, both based on zeolites.
- the wash performance of these three compositions was established in a Zanussi ZF 822W top loading drum washing machine, using the normal 40* C cotton cycleprogramme "C".
- 2.5 kg clean mixed wash load of clean cotton pieces and standard soiled test cloths was processed at a liquor/cloth ratio of approximately 6.
- the water temperature was 20 ° C at a pressure of 2.0 kg/cm2.
- the water hardness was 9 or 25 GH.
- the wash powder was added in a dosage of 7.5 g/I. The differences in reflectance of the test clothes before and after the wash ( R * 460) were recorded.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
Abstract
Description
- The present invention relates to a novel, particulate laundry detergent composition which contains no, or reduced levels of inorganic phosphate compounds. Furthermore, it relates to a particulate base material suitable for use in such detergent compositions and to a method of manufacturing this particulate base material.
- Conventional laundry detergent compositions contain phosphate compounds, especially sodium tripolyphosphate (STP), as building agents. Owing to the negative effects of phosphates on the environment, there has been an increasing interest in developing new laundry detergent compositions which have a low or zero phosphate content. However, it has proved to be difficult to match the excellent builder properties of the phosphate-containing compositions.
- It is known to use zeolites as builder in zero-P laundry detergent formulations. However, the application of zeolites in laundry detergent formulations has a number of drawbacks. In the first place, zeolites have a tendency to cause a bad powder structure. Further more, they tend to interact with silicates which are usually present in the composition as anti-corrosion agents, and they can cause dispensing problems in the washing machine and incrustation on the washed fabrics.
- We have now found that in accordance with the present invention a new low- or zero-P particulate laundry detergent composition can be provided, without the need for zeolites. The compositions of the invention utilise acid soap both as a powder base and as a builder:
- The composition according to the invention comprises as a first particulate material a fatty acid mixture in which up to 35 mole% may be unsaturated fatty acids, which mixture has been neutralised to an extent of 25-60 mole %, and as a second particulate material a base in an amount sufficient to render the pH of the composition at a 0.5 wt% concentration in water higher than 8.
- Optionally conventional detergent additives may be present, such as a bleach system, proteolytic enzymes, anti-foaming agents, optical brighteners, perfumes, anti-corrosion additives, etc.
- The composition according to the invention exhibits very satisfactory wash performance without the need for phosphate or zeolite builders, although the presence of low levels of these materials is not prohibited and may be beneficial. Powder properties such as flow and compressibility are also excellent. The particulate laundry detergent composition according to the invention preferably contains 30-80 wt.% of granular acid soap particles.
- The acid soap is a mixture of free fatty acids and soap, or a partially neutralized mixture of fatty acids. In principle, a wide range of saturated and/or unsaturated fatty acids may be used, but it was found that the powder properties of the particulate composition become less favourable at a content of unsaturated fatty acids of more than 35 mole%. More specifically, such powders tend to be sticky and are barely free-flowing. The lower the proportion of saturated fatty acid of chain length <C14 present, the greater the proportion of unsaturated fatty acids that can be tolerated.
- Preferably, the mixture of fatty acid consists essentially of 5 - 20 mole% C16-C18 unsaturated fatty acids, and 95 - 80 mole% of a mixture of C8-C14 saturated fatty acids and C16-C18 saturated fatty acids in a ratio of 3:1-1:2.
- For the purpose of this invention, the following definitions will be used: C8-C14 saturated fatty acids will also be referred to as laurics, C14-C16 saturated fatty acids as stearics and C16-C18 unsaturated fatty acids as oleics.
- In the mixture of fatty acids, the C16-C18 saturated fatty acids or stearics are mainly responsible for the builder properties, while they contribute little to detergency. The C16-C18 unsaturated fatty acids or oleics are important for their builder properties but especially for detergency. The C8-C14 saturated fatty acids or laurics contribute both to the building and to the detergency, but their main function is to facilitate processing of the soap/fatty acid mixture, and to ensure adequate dissolution properties.
- The laundry detergent compositions according to the present invention can be prepared by dry-mixing the various ingredients into a suitable mixture.
- According to the invention, the acid soap is used in the form of a particulate material, for example, prills or noodles. Particle size and shape may be chosen at will and are discussed in more detail below. These acid soap particles can be prepared by dissolving a suitable amount of soap in a mixture of fatty acid in the molten state, followed by solidification and processing of the solid mass. Alternatively, they can be prepared by partial in situ saponification or neutralization of a mixture of fatty acids. In this process, a solid base material is gradually admixed with the molten fatty acid mixture. Suitable basic compounds are, for example, soda ash (sodium carbonate), sodium disilicate or metasilicate, or sodium hydroxide. When soda ash is used, only C02 is formed as a by-product, which is easily removed from the reaction mixture. When using sodium alkaline silicates, the formation of insoluble silicates may lead to a higher viscosity of the molten soap/fatty acid mixture. On the other hand, incorporation of silicates directly in the soap/fatty acid matrix is advantageous for the powder structure, and problems associated with the dry mixing of silicates as such are avoided. The operating temperature required to process these mixtures increases with the fatty acid chain length and degree of neutralization, and is preferably within the range of 70-140 C.
- Furthermore, the detergent composition of the present invention contains a particulate base in an amount sufficient to render the pH of the composition, at a 0.5 wt.% concentration in water, higher than 8. As a base material, in principle any base can be used which can be prepared in a particulate form and which readily dissolves in water without forming precipitates with the soap fatty acid particles. Preferably, the same base is used as for the partial neutralization of the fatty acid mixture.
- The laundry detergent composition according to the invention may additionally contain other detergent compounds, such as anionic and/or nonionic non-soap detergent-active compounds. These may be incorporated in the particulate acid soap base, or present as a separate ingredient. The acid soap particles may contain up to 10% by weight of anionic and/or nonionic surfactant: higher levels can be detrimental to powder properties.
- Alternatively or additionally, anionic or nonionic surfactants, but especially nonionic surfactants, may be carried on a porous inorganic material which is admixed with the acid soap particles. An example of such an adjunct is a liquid ethoxylated C13-C15 alcohol sprayed on to a Burkeite carrier. If the inorganic carrier is a basic material, the adjunct may serve as the basic component (second particulate material) of the composition.
- A particularly preferred method of preparing acid soap particles was found to be spray-cooling. It was found thereby that particles or prills are obtained with excellent properties with regard to the dissolution rate, stability and to wash performance of the complete detergent composition.
- Using the spray-cooling process, prills of any desired size and bulk density can be obtained by manipulation of the process conditions. Prills of average particle size 250-1000 m and buk density 400-750 g/e are preferred for compatibility with the other solid ingredients of the compsition, so that segregation in the pack is minimised.
- When following the soap/fatty acid spray-cooling route, apart from the builder/active and solubility requirements, a number of additional factors should be considered:
- 1. To ensure adequate handling and storage properties, the soap/fatty acid-mixture should be sufficiently solid at temperatures below 35-40 C.
- 2. For processing reasons, complete liquefaction should preferably be possible below 100°C. In practice, this means a maximum mixing temperature <150 C. It was found that meeting this requirement means that the soap content of the mixture should be limited to 25-60 mole%, depending on the fatty acid composition.
- 3. The composition of the mixture, in terms of fatty acid types and degree of neutralization, should be such as to ensure adequate solubility at low wash peratures, i.e. in the 20-40° C region.
- It will be clear to the man skilled in the art that these requirements are not easy to fulfil at the same time. A number of characteristics of soap/fatty acid mixtures have to be considered.
- Firstly, soaps as well as fatty acids may form various eutectic complexes; such complexes may also be formed between soaps and fatty acids, resulting in highly' complicated phase diagrams for such mixtures. This aspect is particularly relevant to the question of meeting the 35-40 ° C target for the solidification temperature. In addition, it was found that preferably the relative amounts of laurics and stearics should not exceed a 1:1 ratio; nevertheless, some liquefaction at the eutectic temperature of about 33 C cannot be avoided. Although not ideal from a handling/stability point of view, the presence of some low melting laurics/stearics complex may be expected to have a favourable effect on the low temperature solubility.
- Secondly, a further complication arises from the phenomenon of metathesis; addition of soap to a fatty acid mixture will lead to equilibration reactions, resulting in the presence of soap and free acids for all chain length homologues in a specific ratio, depending on the reactivity of the individual acids. Fortunately, the reactivities of unsaturated and saturated acids differ to such an extent that in a practical situation in these mixtures, the oleics will be preferentially converted into soap. Significant amounts of lauric soap and stearic soap can only present when the proportion of soap exceeds that of oleate.
- The invention will now be illustrated by the following Examples.
- A number of fatty acid mixtures were prepared, having the compositions shown in Table A. The mixtures were then heated and at approximately 65. C they began to melt. Heating was continued and after complete melting at a temperature of about 80 C soda ash (sodium carbonate) was gradually added in an amount of 0.1 kg/min to control the C02-evolution until the desired degree of neutralization had been reached. At the same time, the temperature was gradually raised to approximately 140` C.
- Subsequently, the partially neutralized fatty acid mixture was allowed to cool until solidification had occurred. The solid mass was noodled, using a sodium press. Noodles having a diameter of 1 mm and a length of about 5 mm were obtained. The properties of the noodles and the handling properties are shown in Table A. The solubility was measured as follows: The rate of dissolution of the soap/fatty acid noodles was determined by monitoring the increase in conductivity resulting from dissolution of the soap part of the noodles. In this method, 3 g/I of the sample is added to 1 I demineralized water at 25. C with continuous stirring, using a magnetic stirrer. The rate of dissolution is expressed as the time required to dissolve 50% of the soluble part of the soap/fatty acid blend (t½) . The maximum conductivity is measured after heating to above the melting temperature of the fatty acids, followed by cooling down to ambient temperature.
-
-
- From comparison of Examples 1-3 with 4-6 it follows that by spray-cooling the partially neutralized fatty acid mixtures, prills are obtained having particularly advantageous solubility and powder properties.
- A mixture of fatty acids was prepared, having thefollowing composition :
- 20 wt.% oleics
- 45 wt.% C12-C14 fatty acids
- 35 wt.% stearics
-
- The procedure of Example 7 was repeated, using a fatty acid mixture of the following composition :
- 30 wt.% oleics
- 40 wt.% C12-C14 fatty acids
- 30 wt.% stearics
- The acid soap prills obtained according to Example 7 were used to formulate a complete laundry detergent composition by dry-mixing various other ingredients to the prills, such as a nonionic detergent on a Burkeite carrier, a bleach system and an enzyme.
- The composition of the complete detergent powder is given in Table E. Also shown are two commercially available laundry detergent compositions, composition B being a low-P and composition A a zero P composition, both based on zeolites.
- The wash performance of these three compositions was established in a Zanussi ZF 822W top loading drum washing machine, using the normal 40* C cotton cycleprogramme "C". 2.5 kg clean mixed wash load of clean cotton pieces and standard soiled test cloths was processed at a liquor/cloth ratio of approximately 6. The water temperature was 20 ° C at a pressure of 2.0 kg/cm2. The water hardness was 9 or 25 GH. The wash powder was added in a dosage of 7.5 g/I. The differences in reflectance of the test clothes before and after the wash ( R*460) were recorded.
- The results of the tests at the two different degrees of water hardness using four different test cloths, including the standard EMPA-101 and WFK-10C cloths, are shown in Table F. From these results it is clear that, even at a high water hardness, a very satisfactory washing performance was observed, despite the fact that no phosphate or zeolite builder was present.
The mixture was heated to 65 C and, under continuous heating, solid sodium carbonate was added until a degree of saponification of 33% was reached. The molten soap/fatty acid mixture was subsequently spray-cooled at a temperature of 110 °C, using the conditions given in Table B.
The molten fatty acid mixture was partially neutralized, using solid sodium disilicate, and subsequently spray-cooled. The properties of the prills obtained are given in Table D above and indicate highly satisfactory handling properties.
Claims (15)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8803263 | 1988-02-12 | ||
GB888803263A GB8803263D0 (en) | 1988-02-12 | 1988-02-12 | Particulate laundry detergent composition |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0328190A2 true EP0328190A2 (en) | 1989-08-16 |
EP0328190A3 EP0328190A3 (en) | 1990-10-24 |
EP0328190B1 EP0328190B1 (en) | 1994-05-04 |
Family
ID=10631597
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19890200221 Expired - Lifetime EP0328190B1 (en) | 1988-02-12 | 1989-02-02 | Particulate laundry detergent composition |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0328190B1 (en) |
JP (1) | JPH0668120B2 (en) |
DE (1) | DE68915015T2 (en) |
ES (1) | ES2051983T3 (en) |
GB (1) | GB8803263D0 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0350189A2 (en) * | 1988-07-07 | 1990-01-10 | City Of Hope National Medical Center | Multi-specimen slides for immunohistologic procedures |
US5935923A (en) * | 1996-09-10 | 1999-08-10 | Lever Brothers Company, Division Of Conopco, Inc. | Process for preparing high bulk density detergent compositions |
US20150017311A1 (en) * | 2013-07-02 | 2015-01-15 | Milk Specialties Global | Partial neutralization of free fatty acid mixtures with potassium, livestock feed compositions including them, and methods of making same |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011246682A (en) * | 2010-05-24 | 2011-12-08 | Touki Corp | Powdered detergent |
CN113728083A (en) * | 2019-04-29 | 2021-11-30 | 宝洁公司 | Process for preparing laundry detergent composition |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB989007A (en) * | 1961-01-23 | 1965-04-14 | Procter & Gamble | Detergent bar |
GB1287625A (en) * | 1969-08-25 | 1972-09-06 | Procter & Gamble Ltd | Improved toilet soap |
GB2010894A (en) * | 1977-12-26 | 1979-07-04 | Kao Corp | Soap for scouring pad |
EP0042647A1 (en) * | 1980-06-20 | 1981-12-30 | Unilever N.V. | Particulate, soap-containing detergent composition |
EP0470033A2 (en) * | 1990-08-01 | 1992-02-05 | Asturiana De Zinc, S.A. | Installation for removing the zinc deposited by electrolysis on aluminium plates |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5230962B2 (en) * | 1972-12-12 | 1977-08-11 | ||
JPS5231202B2 (en) * | 1973-11-01 | 1977-08-13 |
-
1988
- 1988-02-12 GB GB888803263A patent/GB8803263D0/en active Pending
-
1989
- 1989-02-02 DE DE1989615015 patent/DE68915015T2/en not_active Expired - Fee Related
- 1989-02-02 EP EP19890200221 patent/EP0328190B1/en not_active Expired - Lifetime
- 1989-02-02 ES ES89200221T patent/ES2051983T3/en not_active Expired - Lifetime
- 1989-02-10 JP JP1032558A patent/JPH0668120B2/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB989007A (en) * | 1961-01-23 | 1965-04-14 | Procter & Gamble | Detergent bar |
GB1287625A (en) * | 1969-08-25 | 1972-09-06 | Procter & Gamble Ltd | Improved toilet soap |
GB2010894A (en) * | 1977-12-26 | 1979-07-04 | Kao Corp | Soap for scouring pad |
EP0042647A1 (en) * | 1980-06-20 | 1981-12-30 | Unilever N.V. | Particulate, soap-containing detergent composition |
EP0470033A2 (en) * | 1990-08-01 | 1992-02-05 | Asturiana De Zinc, S.A. | Installation for removing the zinc deposited by electrolysis on aluminium plates |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0350189A2 (en) * | 1988-07-07 | 1990-01-10 | City Of Hope National Medical Center | Multi-specimen slides for immunohistologic procedures |
EP0350189A3 (en) * | 1988-07-07 | 1991-05-29 | City Of Hope National Medical Center | Multi-specimen slides for immunohistologic procedures |
US5935923A (en) * | 1996-09-10 | 1999-08-10 | Lever Brothers Company, Division Of Conopco, Inc. | Process for preparing high bulk density detergent compositions |
US20150017311A1 (en) * | 2013-07-02 | 2015-01-15 | Milk Specialties Global | Partial neutralization of free fatty acid mixtures with potassium, livestock feed compositions including them, and methods of making same |
Also Published As
Publication number | Publication date |
---|---|
GB8803263D0 (en) | 1988-03-09 |
DE68915015T2 (en) | 1994-08-18 |
JPH0668120B2 (en) | 1994-08-31 |
EP0328190B1 (en) | 1994-05-04 |
DE68915015D1 (en) | 1994-06-09 |
EP0328190A3 (en) | 1990-10-24 |
ES2051983T3 (en) | 1994-07-01 |
JPH01268799A (en) | 1989-10-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU2143998C1 (en) | Sodium silicates as structure-forming agent, compound and washing agents or detergents comprising them | |
CA1290640C (en) | Antifoam ingredient | |
US3318817A (en) | Process for preparing detergent tablets | |
JPS61111400A (en) | Bleaching composition | |
AU593602B2 (en) | Soap encapsulated bleach particles | |
ZA200101221B (en) | Particulate laundry detergent compositions containing nonionic surfactant granules. | |
CA1303939C (en) | Detergent granules and a process for their preparation | |
CZ283895A3 (en) | Process for preparing granulated detergent component or composition | |
JPS6024160B2 (en) | cleaning composition | |
NO153338B (en) | Particulate bleach and its use | |
EP0328190B1 (en) | Particulate laundry detergent composition | |
CA1322705C (en) | Process for making concentrated surfactant granules | |
KR950004823B1 (en) | Soap powder compositions | |
JP3841431B2 (en) | Spray-dried detergent or its components | |
US4549978A (en) | Process for manufacture of detergent powder | |
CA1337041C (en) | Granular detergent compositions having improved solubility | |
EP1185602A1 (en) | Particulate detergent composition containing zeolite | |
EP0436240B2 (en) | Process for preparing a high bulk density detergent composition having improved dispensing properties | |
JPH0354158B2 (en) | ||
JPS6189300A (en) | Production of granular detergent composition containing nonionic surfactant | |
WO1995012453A1 (en) | Surfactant agglomerate particle | |
JPS6410040B2 (en) | ||
PL177812B1 (en) | Detergent composition containing a grafted copolymer | |
EP0700427B1 (en) | Detergent compositions | |
JP2672814B2 (en) | High density granular detergent composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): CH DE ES FR GB IT LI NL SE |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
RHK1 | Main classification (correction) |
Ipc: C11D 9/26 |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): CH DE ES FR GB IT LI NL SE |
|
17P | Request for examination filed |
Effective date: 19901009 |
|
RAP3 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: UNILEVER PLC Owner name: UNILEVER N.V. |
|
17Q | First examination report despatched |
Effective date: 19930614 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): CH DE ES FR GB IT LI NL SE |
|
REF | Corresponds to: |
Ref document number: 68915015 Country of ref document: DE Date of ref document: 19940609 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2051983 Country of ref document: ES Kind code of ref document: T3 |
|
ET | Fr: translation filed | ||
ITF | It: translation for a ep patent filed | ||
EAL | Se: european patent in force in sweden |
Ref document number: 89200221.3 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19970129 Year of fee payment: 9 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19980228 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19980228 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20000223 Year of fee payment: 12 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20010111 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20010117 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20010119 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20010129 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20010213 Year of fee payment: 13 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20010901 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 20010901 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020202 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020203 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020204 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020903 |
|
EUG | Se: european patent has lapsed |
Ref document number: 89200221.3 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20020202 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20021031 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20031022 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED. Effective date: 20050202 |