CA1149296A - Laundry pre-treating cleaning composition - Google Patents
Laundry pre-treating cleaning compositionInfo
- Publication number
- CA1149296A CA1149296A CA000345117A CA345117A CA1149296A CA 1149296 A CA1149296 A CA 1149296A CA 000345117 A CA000345117 A CA 000345117A CA 345117 A CA345117 A CA 345117A CA 1149296 A CA1149296 A CA 1149296A
- Authority
- CA
- Canada
- Prior art keywords
- weight
- composition according
- moles
- composition
- ethylene oxide
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 46
- 238000004140 cleaning Methods 0.000 title claims abstract description 6
- 239000003599 detergent Substances 0.000 claims abstract description 18
- 102000004190 Enzymes Human genes 0.000 claims abstract description 15
- 108090000790 Enzymes Proteins 0.000 claims abstract description 15
- 239000007788 liquid Substances 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003960 organic solvent Substances 0.000 claims abstract description 9
- 239000002904 solvent Substances 0.000 claims description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- 238000002203 pretreatment Methods 0.000 claims description 8
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 150000003138 primary alcohols Chemical class 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 5
- 238000009835 boiling Methods 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 4
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- 150000003333 secondary alcohols Chemical class 0.000 claims description 3
- -1 trichloroethylene, tetrachloroethylene Chemical group 0.000 claims description 3
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 claims description 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 claims description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 2
- 241000779819 Syncarpia glomulifera Species 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical group 0.000 claims description 2
- 230000003625 amylolytic effect Effects 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229950005499 carbon tetrachloride Drugs 0.000 claims description 2
- 230000005484 gravity Effects 0.000 claims description 2
- 230000002366 lipolytic effect Effects 0.000 claims description 2
- 239000003209 petroleum derivative Substances 0.000 claims description 2
- 239000001739 pinus spp. Substances 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 229940036248 turpentine Drugs 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 1
- OPFTUNCRGUEPRZ-QLFBSQMISA-N Cyclohexane Natural products CC(=C)[C@@H]1CC[C@@](C)(C=C)[C@H](C(C)=C)C1 OPFTUNCRGUEPRZ-QLFBSQMISA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000002689 soil Substances 0.000 abstract description 6
- 229940088598 enzyme Drugs 0.000 description 13
- 230000002255 enzymatic effect Effects 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 108091005804 Peptidases Proteins 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 235000014469 Bacillus subtilis Nutrition 0.000 description 3
- 102000035195 Peptidases Human genes 0.000 description 3
- 239000004365 Protease Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 229960004418 trolamine Drugs 0.000 description 3
- 239000004471 Glycine Substances 0.000 description 2
- 108010056079 Subtilisins Proteins 0.000 description 2
- 102000005158 Subtilisins Human genes 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 150000001414 amino alcohols Chemical class 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000002538 fungal effect Effects 0.000 description 2
- 239000003752 hydrotrope Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 108010059892 Cellulase Proteins 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 229940025131 amylases Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229940106157 cellulase Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001461 cytolytic effect Effects 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229940015607 hydro 40 Drugs 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 108010003855 mesentericopeptidase Proteins 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000375 suspending agent Substances 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38618—Protease or amylase in liquid compositions only
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38663—Stabilised liquid enzyme compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/43—Solvents
Abstract
C 568 (R) Abstract of the Disclosure The invention pertains to the fabric-cleaning art.
Aqueous, liquid laundry pre-spotting compositions are provided comprising a nonionic detergent, an organic solvent, water, enzymes and an alkanolamine.
These compositions are clear, stable and isotropic and are efficaceous against fatty and proteinaceous soils.
Aqueous, liquid laundry pre-spotting compositions are provided comprising a nonionic detergent, an organic solvent, water, enzymes and an alkanolamine.
These compositions are clear, stable and isotropic and are efficaceous against fatty and proteinaceous soils.
Description
- 1 - C 568 (R) LAUNDRY PRE-TREATMENT CLEANING COMPOSITION
The present invention relates to a laundry pre-treatment cleaning composition. Such a cleaning composition is used to treat, prior to the usual laundering and washing process with common detergent compositi ons, heavily soiled areas of the fabri cs to be cleaned, so as to make the removal of the soil from those areas in the subsequent washing process more effective. Such areas are, for example, collars, cuffs, brims of shirts, underwear, which may be heavily soiled with human sebum, as well as industrial clothing, which may become heavily soiled by external soil-sources, not only ~ats and oils, but also blood and the like.
Such pre-treatment compositions, also known as pre-spotting compositi ons, are as a type of product not unknown in the detergent industry. They normally comprise a m~xture of a suitable organic solvent and a suitable detergent active material, optionally with further desirable additives. Normally, the detergent-active material is a nonionic surfactant, and the organic solvent may be one of the many solvents known in the art. Typical examples of such pre-spotting compositions are described in German Paten t Appli cations
The present invention relates to a laundry pre-treatment cleaning composition. Such a cleaning composition is used to treat, prior to the usual laundering and washing process with common detergent compositi ons, heavily soiled areas of the fabri cs to be cleaned, so as to make the removal of the soil from those areas in the subsequent washing process more effective. Such areas are, for example, collars, cuffs, brims of shirts, underwear, which may be heavily soiled with human sebum, as well as industrial clothing, which may become heavily soiled by external soil-sources, not only ~ats and oils, but also blood and the like.
Such pre-treatment compositions, also known as pre-spotting compositi ons, are as a type of product not unknown in the detergent industry. They normally comprise a m~xture of a suitable organic solvent and a suitable detergent active material, optionally with further desirable additives. Normally, the detergent-active material is a nonionic surfactant, and the organic solvent may be one of the many solvents known in the art. Typical examples of such pre-spotting compositions are described in German Paten t Appli cations
2,021,677, 1,279,273 and in US Patent Specification 3,872,021. Most of these compositions are liquid compositions cDntaining a relatively small amount of water.
However, although these products often satisfactorily remove several typesoffattysoils and -stains, they do not do so when the garments are soiled with several types of ~ther organic soils such as proteins, - 2 - C 568 (R) blood and the like.
The present invention aims at improving such products in their overall stain-removal properties, particularly as regards the removal of the above organic soils, besides the fatty soil.
It has already been proposed in US Patent Specification 3,953,353 to include an enzyme in a solid pre-spotting composition to enhance the stain-removal properties of common pre-spotting compositions. In US Patent Specification 3,741,902 a liquid pre-spotting composition is proposed which contains a liquid nonionic detergent, an organic solvent, and an enzyme. These prior proposals, however, dissuade the use of an aqueous liquid composition, since the presence of water may cause gelling, or may jeopardize the efficacy of the enzymes.
The present invention aims at providing an aqueous liquid enzyme-containing pre-spotting composition which is a clear, isotropic liquid and in which the enzymes maintain their efficacy. It has now been found that the incorporation of an alkanolamine in a pre-spotting composition containing a nonionic detergent, an organic solvent, an enzyme and water, provides for an efficaceous, stable, clear and isotropic liquid pre-spotting composition.
In German Patent Application 1,617,119 a liquid pre-spotting composition is disclosed, which contains a mixture of t~o different classes oF nonionics3 a solvent, a hydrotrope and optionally water. Among the solvents also amino alcohols are mentioned. ~owever, there is no disclosure of the possibility to include enzymes in these compositions, nor any indication that especially the amino alcohols should be selected, together with organic solvents, if one wishes to incorporate enzymes.
The present invention therefore provides a liquid water-containing pre-spotting composition, comprising:
2~3~
However, although these products often satisfactorily remove several typesoffattysoils and -stains, they do not do so when the garments are soiled with several types of ~ther organic soils such as proteins, - 2 - C 568 (R) blood and the like.
The present invention aims at improving such products in their overall stain-removal properties, particularly as regards the removal of the above organic soils, besides the fatty soil.
It has already been proposed in US Patent Specification 3,953,353 to include an enzyme in a solid pre-spotting composition to enhance the stain-removal properties of common pre-spotting compositions. In US Patent Specification 3,741,902 a liquid pre-spotting composition is proposed which contains a liquid nonionic detergent, an organic solvent, and an enzyme. These prior proposals, however, dissuade the use of an aqueous liquid composition, since the presence of water may cause gelling, or may jeopardize the efficacy of the enzymes.
The present invention aims at providing an aqueous liquid enzyme-containing pre-spotting composition which is a clear, isotropic liquid and in which the enzymes maintain their efficacy. It has now been found that the incorporation of an alkanolamine in a pre-spotting composition containing a nonionic detergent, an organic solvent, an enzyme and water, provides for an efficaceous, stable, clear and isotropic liquid pre-spotting composition.
In German Patent Application 1,617,119 a liquid pre-spotting composition is disclosed, which contains a mixture of t~o different classes oF nonionics3 a solvent, a hydrotrope and optionally water. Among the solvents also amino alcohols are mentioned. ~owever, there is no disclosure of the possibility to include enzymes in these compositions, nor any indication that especially the amino alcohols should be selected, together with organic solvents, if one wishes to incorporate enzymes.
The present invention therefore provides a liquid water-containing pre-spotting composition, comprising:
2~3~
- 3 - C 568 (R) a) from 10-50% by weight of a nonionic detergent;
b) from 20-60% by weight of an organic solvent;
c) from 5-20% by weight of water;
d) from 0.001-20% by weight of an enzymej and e) from 0.5-20% by weight of an alkanol amine.
The nonionic detergent to be used in the present invention is an ethoxylated and/or propoxylated primary or secondary alcohol, or alkylphenol. The ethoxylation and/or propoxylation degree may vary rather widely, i.e. the nonionic detergent may contain from 1-30 moles of ethylehe oxide or from 1-30 moles of propylene oxide.
When the nonionic detergent contains both ethylene oxide and propylene oxide, the latter is present in smaller amounts than the former. The primary or secondary alcohol contains from 11-24 carbon atoms. Mixtures of nonionic detergents may also be used. Typical examples of suitable nonionics are linear sec.
C11-C~5 alcohols, condensed with 7, 9 or 12 moles of ethylene oxide, linear primary C12-C15 alcohols condense~ with 7 or 12 moles of ethylene oxide, C13-C15 primary alcohols,condensed with 7 moles of ethylene oxide plus propylene oxide, -in which the weight ratio oF
ethylene oxide to propylene oxide is ~38:12 or 92:8.
The preferred amount of nonionic detergent in the composition is from 20-40% by weight.
The organic solvents to be used in the invention are the well-known solvents, miscible with the above nonionic detergents. Typical examples are dry-cleaning solvents such as petroleum distillates, carbontetrachloride, trichloroethylene, tetrachloroethylene, turpentine, cyclohexane, benziine; furthermore paraffins such as decane, dodecane; alcohols such as isopropanol, hexanol, tridecanol;
ketones, such as acetone,glycols such as ethylene glycols, and ethers such as diethylene glycol monomethylether.
A preferred solvent is a high-boiling aliphatic hydrocarbon having a specific gravity of 0.76, a boiling range of 187-212C and a flame point of 58C (Pensky Martens). This solvent is manufactured and sold 92~36
b) from 20-60% by weight of an organic solvent;
c) from 5-20% by weight of water;
d) from 0.001-20% by weight of an enzymej and e) from 0.5-20% by weight of an alkanol amine.
The nonionic detergent to be used in the present invention is an ethoxylated and/or propoxylated primary or secondary alcohol, or alkylphenol. The ethoxylation and/or propoxylation degree may vary rather widely, i.e. the nonionic detergent may contain from 1-30 moles of ethylehe oxide or from 1-30 moles of propylene oxide.
When the nonionic detergent contains both ethylene oxide and propylene oxide, the latter is present in smaller amounts than the former. The primary or secondary alcohol contains from 11-24 carbon atoms. Mixtures of nonionic detergents may also be used. Typical examples of suitable nonionics are linear sec.
C11-C~5 alcohols, condensed with 7, 9 or 12 moles of ethylene oxide, linear primary C12-C15 alcohols condense~ with 7 or 12 moles of ethylene oxide, C13-C15 primary alcohols,condensed with 7 moles of ethylene oxide plus propylene oxide, -in which the weight ratio oF
ethylene oxide to propylene oxide is ~38:12 or 92:8.
The preferred amount of nonionic detergent in the composition is from 20-40% by weight.
The organic solvents to be used in the invention are the well-known solvents, miscible with the above nonionic detergents. Typical examples are dry-cleaning solvents such as petroleum distillates, carbontetrachloride, trichloroethylene, tetrachloroethylene, turpentine, cyclohexane, benziine; furthermore paraffins such as decane, dodecane; alcohols such as isopropanol, hexanol, tridecanol;
ketones, such as acetone,glycols such as ethylene glycols, and ethers such as diethylene glycol monomethylether.
A preferred solvent is a high-boiling aliphatic hydrocarbon having a specific gravity of 0.76, a boiling range of 187-212C and a flame point of 58C (Pensky Martens). This solvent is manufactured and sold 92~36
- 4 - C 568 (R) under the tradename "Shellsol T" by the Shell Company. Mixtures of different solvents may also be used. The preferred amount of solvent is from 25-50% by weight.
The enzymes to be used in the present invention are proteolytic, amylolytic, lipolytic or cellulolytic enzymes or mixtures thereof.
They are preferably of bacterial or fungal ori~lin. Typical examples are Alcalase ~, Esperase ~ axatase ~ all proteases from B. subtilis, Maxamyl ~ and Thermamyl (~. all amylases of B. subtilis or g. liGheniformis~ ~ipase ~ly ~, a bacterial lipase ex Meiji Co., ~apan, and ~eicelase R, a fungal cellulase ex Meiji Co., Japan.
The amount of enzyme is mostly governed by its activity, and is by weight from 0.001-20,~, preferably 0.001-10%. For proteases a preferred amount is equal to 1-15 glycine unitsJmg.
The alkanol amine to be used in the present invention is a mono-, di- or trialkanol amine in which the alkanol group is a methanol, ethanol, propanol or isopropanol group. ~ preferred alkanol amine is triethanol amine. The preferred amount of alkanol amine is from
The enzymes to be used in the present invention are proteolytic, amylolytic, lipolytic or cellulolytic enzymes or mixtures thereof.
They are preferably of bacterial or fungal ori~lin. Typical examples are Alcalase ~, Esperase ~ axatase ~ all proteases from B. subtilis, Maxamyl ~ and Thermamyl (~. all amylases of B. subtilis or g. liGheniformis~ ~ipase ~ly ~, a bacterial lipase ex Meiji Co., ~apan, and ~eicelase R, a fungal cellulase ex Meiji Co., Japan.
The amount of enzyme is mostly governed by its activity, and is by weight from 0.001-20,~, preferably 0.001-10%. For proteases a preferred amount is equal to 1-15 glycine unitsJmg.
The alkanol amine to be used in the present invention is a mono-, di- or trialkanol amine in which the alkanol group is a methanol, ethanol, propanol or isopropanol group. ~ preferred alkanol amine is triethanol amine. The preferred amount of alkanol amine is from
5-15% by weight. The e~mposition of the invention may furthermore comprise other desirable ingredients in minor amounts. Such ingredients are perfumes, dyes, germicides, evaporation retarders, hydrotropes, soil-suspending agents, and flash-point increasing agents.
The compositions of the invention are normally used prior to a main-wash operation; they can be applied to the fabrics to be treated by simply applying the liquid thereon with the finger or dipping it on.
The invention will now be further illustrated by way of Example.
Example I
The following liquid pre-spotting composition was prepared as follows:
2~6 - 5 - C 568 (R) The enzyme was dispersed in water, and subsequently triethanol amine was added. The resulting mixture was stirred into a mixture of the nonionic and the solvent at room temperature.
~ by weight C13 1~ primary alcohol condensed with 7 moles of ethylene oxide plus propylene 40 oxide (weight ratio of EO:P0=92:8) Solvent "Shellsol T", a high boiling hydro- 40 carbon with a boiling range of 187-212C
Alcalase~) ex Novo Industri AS, a in an amount, bacterial protease from B.subtilis equivalent to 10 glycine units/mg water 10 triethanol amine 10 This composition, which was a stable, non-gelling composition, was used to pre-treat soiled test pieces, which were subsequently washed in a normal washing machine under normal conditions. A
comparison was made ~ith test-pieces, also washed under the same conditions, but without a pre-treatment, or with a pre-treatment with the above composition, in which the enzymes had been left out.
The test pieces were standard test piec:es, soiled with a standard soil (AS 10, Empa 116 or Empa and bloocl). The pre-spotting composition was applied by dipping it on the dry fabric, at ambient temperature. The test pieces were then washed in a Philips HN 3156 washing machine, using the C 4/5 programme in 12 l. water at 8 German hardness at temperatures of 20, 40 and 60C with a commercially available heavy-duty detergent powder with and without proteolytic enzymes.
The following results were obtained (the figures denote mean detergency values in %):
~9~96
The compositions of the invention are normally used prior to a main-wash operation; they can be applied to the fabrics to be treated by simply applying the liquid thereon with the finger or dipping it on.
The invention will now be further illustrated by way of Example.
Example I
The following liquid pre-spotting composition was prepared as follows:
2~6 - 5 - C 568 (R) The enzyme was dispersed in water, and subsequently triethanol amine was added. The resulting mixture was stirred into a mixture of the nonionic and the solvent at room temperature.
~ by weight C13 1~ primary alcohol condensed with 7 moles of ethylene oxide plus propylene 40 oxide (weight ratio of EO:P0=92:8) Solvent "Shellsol T", a high boiling hydro- 40 carbon with a boiling range of 187-212C
Alcalase~) ex Novo Industri AS, a in an amount, bacterial protease from B.subtilis equivalent to 10 glycine units/mg water 10 triethanol amine 10 This composition, which was a stable, non-gelling composition, was used to pre-treat soiled test pieces, which were subsequently washed in a normal washing machine under normal conditions. A
comparison was made ~ith test-pieces, also washed under the same conditions, but without a pre-treatment, or with a pre-treatment with the above composition, in which the enzymes had been left out.
The test pieces were standard test piec:es, soiled with a standard soil (AS 10, Empa 116 or Empa and bloocl). The pre-spotting composition was applied by dipping it on the dry fabric, at ambient temperature. The test pieces were then washed in a Philips HN 3156 washing machine, using the C 4/5 programme in 12 l. water at 8 German hardness at temperatures of 20, 40 and 60C with a commercially available heavy-duty detergent powder with and without proteolytic enzymes.
The following results were obtained (the figures denote mean detergency values in %):
~9~96
- 6 - C 568 (R) ~ o~ ~ _ ~ ; ~
a) E u> ~ ~ Ln 1` ~ u~ r_ d o~' QO~ ~ u~ O L~ D `D ~ ~1 a~ . ~) ~ N _ _ 1S~ ~D d' , O Lr~ 1~ LO n ~t ~ L~
~1 ~1 ~I N ~ ~1 ~1 ~1 ~1 ,-1 ~ ~/) _ _ . _ _ E o o o o o o o o o E u~
d- ~ d- ~D C E
~1 ~ . _ ~
C~ d' ~ ~ ~; a~ ~ ~ ~_ ~ u ~ s t-~: a~v~ ~ ~ ~ ~ ~ s~
3 ~ _ . _ o 3 3 0~ ~<~ 00 ~ ~ C~ CO ~ ~ 'O ~ ~~
O I o ~ ___ __ E E
~'3 ~ l ~ J ~
--/ _ _ ~Q ~o) ~o ~ ~o ~o ~o -oO ~
/ ~ ~ C~ ~ ~ 0 ~ ~ _ ~S~ _ ~5LLI _ iK
', 92~6 ~ 7 - C 568 (R) Example II
. .
Soaking tests were carried out with and without the (enzymatic) pre-treatment compositions of Example I, with and without an enzymatic detergent composition. The results are shown below:
., 9Z~
_ ~ _ C 568 (R) ~
o o ~ o ~ ~
~ ~ O ~ ~ =r t O ~
~9~
- 9 - C 568 (R) The data of Table I showed that a significantly improved detergency was obtained with the composition of the invention.
On AS 10 and EMPA-116 the non-enzymatic pre-spotting composition did not show much improvement, and on EMPA-blood it sometimes showed a clear increase in detergency, depending on whether the main wash was carried out with an enzymatic or non-enzymatic detergent powder. The pre-treatment with the enzymatic pre-spotting composition of the invention gave on all test pieces and under all test conditions a clear, unexpected detergency improvement.
The same overall picture was shown by the data of Table II.
a) E u> ~ ~ Ln 1` ~ u~ r_ d o~' QO~ ~ u~ O L~ D `D ~ ~1 a~ . ~) ~ N _ _ 1S~ ~D d' , O Lr~ 1~ LO n ~t ~ L~
~1 ~1 ~I N ~ ~1 ~1 ~1 ~1 ,-1 ~ ~/) _ _ . _ _ E o o o o o o o o o E u~
d- ~ d- ~D C E
~1 ~ . _ ~
C~ d' ~ ~ ~; a~ ~ ~ ~_ ~ u ~ s t-~: a~v~ ~ ~ ~ ~ ~ s~
3 ~ _ . _ o 3 3 0~ ~<~ 00 ~ ~ C~ CO ~ ~ 'O ~ ~~
O I o ~ ___ __ E E
~'3 ~ l ~ J ~
--/ _ _ ~Q ~o) ~o ~ ~o ~o ~o -oO ~
/ ~ ~ C~ ~ ~ 0 ~ ~ _ ~S~ _ ~5LLI _ iK
', 92~6 ~ 7 - C 568 (R) Example II
. .
Soaking tests were carried out with and without the (enzymatic) pre-treatment compositions of Example I, with and without an enzymatic detergent composition. The results are shown below:
., 9Z~
_ ~ _ C 568 (R) ~
o o ~ o ~ ~
~ ~ O ~ ~ =r t O ~
~9~
- 9 - C 568 (R) The data of Table I showed that a significantly improved detergency was obtained with the composition of the invention.
On AS 10 and EMPA-116 the non-enzymatic pre-spotting composition did not show much improvement, and on EMPA-blood it sometimes showed a clear increase in detergency, depending on whether the main wash was carried out with an enzymatic or non-enzymatic detergent powder. The pre-treatment with the enzymatic pre-spotting composition of the invention gave on all test pieces and under all test conditions a clear, unexpected detergency improvement.
The same overall picture was shown by the data of Table II.
Claims (5)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. An aqueous liquid laundry pre-treatment cleaning composition, consisting essentially of a) from 10-50% by weight of a nonionic detergent selected from the group consisting of primary and secondary alcohols, containing from 11 to 24 carbon atoms in their alkyl chain, condensed with 1-30 moles of ethylene oxide, 1-30 moles of propylene oxide and mixtures thereof;
b) from 20-60% by weight of an organic solvent selected from the group consisting of petroleum distillates, carbontetrachloride, trichloroethylene, tetrachloroethylene, turpentine, cyclo-hexane, benzine, decane, dodecane, isopranol, hexanol, tridecanol, acetone, ethylene glycol and diethylene glycol monomethylether;
c) from 5-20% of water;
d) from 0.001-20% by weight of an amylolytic, lipolytic or proteolyti c enzyme i e) from 0.5-20% by weight of a mono-, di- or trialkanolamine in whi ch the alkanol group is methanol, ethanol, propanol or isopropanol.
b) from 20-60% by weight of an organic solvent selected from the group consisting of petroleum distillates, carbontetrachloride, trichloroethylene, tetrachloroethylene, turpentine, cyclo-hexane, benzine, decane, dodecane, isopranol, hexanol, tridecanol, acetone, ethylene glycol and diethylene glycol monomethylether;
c) from 5-20% of water;
d) from 0.001-20% by weight of an amylolytic, lipolytic or proteolyti c enzyme i e) from 0.5-20% by weight of a mono-, di- or trialkanolamine in whi ch the alkanol group is methanol, ethanol, propanol or isopropanol.
2. A composition according to claim 1, comprising by weight.
20-40% of a) 25-50% of b) 5-20% of c) 0.001-10% of d) 5-15% of e).
20-40% of a) 25-50% of b) 5-20% of c) 0.001-10% of d) 5-15% of e).
3. A composition according to claim 1, wherein the nonionic detergent is a C13-C15 primary alcohol, condensed with 7 moles of ethylene oxide plus propylene oxide, the weight ratio of ethylene oxide to propylene oxide being 92:8.
4. A composition according to claim 1, wherein the solvent is an aliphatic hydrocarbon having a specific gravity of 0.76, a boiling - 11 - C 568 (R) range of 187-212C and a flame point (Pensky Martens) of 58C.
5. A composition according to claim 1, wherein the alkanolamine is triethanolamine.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7904330 | 1979-02-07 | ||
GB7904330 | 1979-02-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1149296A true CA1149296A (en) | 1983-07-05 |
Family
ID=10503032
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000345117A Expired CA1149296A (en) | 1979-02-07 | 1980-02-05 | Laundry pre-treating cleaning composition |
Country Status (11)
Country | Link |
---|---|
AU (1) | AU534863B2 (en) |
BR (1) | BR8000656A (en) |
CA (1) | CA1149296A (en) |
CH (1) | CH642997A5 (en) |
DE (1) | DE3003766A1 (en) |
FR (1) | FR2448568A1 (en) |
GB (1) | GB2042580B (en) |
GR (1) | GR68421B (en) |
IT (1) | IT1133063B (en) |
NL (1) | NL8000452A (en) |
PT (1) | PT70785B (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3232616A1 (en) * | 1982-09-02 | 1984-03-08 | Henkel KGaA, 4000 Düsseldorf | LIQUID, INORGANIC FRUIT SALT, IN ESSENTIAL FREE DETERGENT AND CLEANING AGENT |
MX161813A (en) * | 1982-12-13 | 1990-12-28 | Colgate Palmolive Co | IMPROVEMENTS TO LIQUID DETERGENT COMPOSITION |
US4530781A (en) * | 1983-10-12 | 1985-07-23 | S. C. Johnson & Son, Inc. | Metastable prespotting composition |
CA1263944A (en) * | 1984-09-12 | 1989-12-19 | Barbara H. Munk | Pre-wash compositions containing enzymes |
US4801544A (en) * | 1984-09-12 | 1989-01-31 | The Clorox Company | Method of improving the storage life of liquid compositions containing enzymes |
CA1283511C (en) * | 1986-09-02 | 1991-04-30 | Colgate-Palmolive | Laundry pre-spotter composition providing improved oily soil removal |
NL8900267A (en) * | 1989-02-03 | 1990-09-03 | Douwe Egberts Tabaksfab | LIQUID CLEANER. |
US5447649A (en) * | 1990-03-01 | 1995-09-05 | Novo Nordisk A/S | Lipase containing liquid pre-spotter and use of such pre-spotter |
DK0517761T3 (en) * | 1990-03-01 | 1994-05-09 | Novo Nordisk As | Lipase-containing liquid pre-spotter and the use of such pre-spotter |
US5910420A (en) * | 1996-08-16 | 1999-06-08 | Orion-Yhtyma Oy Orion Diagnostica | Method and test kit for pretreatment of object surfaces |
US6471728B2 (en) | 1998-05-15 | 2002-10-29 | Ecolab Incorporated | Removal of blood stains |
DE19953870A1 (en) * | 1999-11-10 | 2001-05-17 | Henkel Kgaa | Process for the preparation of a low-water enzyme preparation |
ES2662323T3 (en) | 2010-07-07 | 2018-04-06 | Dalli-Werke Gmbh & Co. Kg | Composition of prewash stains for local laundry application |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3860536A (en) * | 1970-01-02 | 1975-01-14 | Cpc International Inc | Enzyme-detergent combination |
US3781212A (en) * | 1972-10-27 | 1973-12-25 | Townsend & Townsend | Aerosol enzyme detergents stabilized with carbon dioxide |
US4021377A (en) * | 1973-09-11 | 1977-05-03 | Miles Laboratories, Inc. | Liquid detergent composition |
FR2264865A1 (en) * | 1974-03-21 | 1975-10-17 | Procter & Gamble | Heavy duty liq. detergent compsn. - contg. nonionic ethoxylated alcohol surfactant, anionic surfactant neutralised with alkanolamine and free alkanolamine |
CA1044983A (en) * | 1974-03-21 | 1978-12-26 | The Procter And Gamble Company | Liquid detergent compositions |
-
1980
- 1980-01-24 NL NL8000452A patent/NL8000452A/en not_active Application Discontinuation
- 1980-02-01 DE DE19803003766 patent/DE3003766A1/en not_active Ceased
- 1980-02-01 BR BR8000656A patent/BR8000656A/en not_active IP Right Cessation
- 1980-02-02 GR GR61110A patent/GR68421B/el unknown
- 1980-02-05 FR FR8002479A patent/FR2448568A1/en active Granted
- 1980-02-05 CH CH92280A patent/CH642997A5/en not_active IP Right Cessation
- 1980-02-05 CA CA000345117A patent/CA1149296A/en not_active Expired
- 1980-02-06 PT PT70785A patent/PT70785B/en unknown
- 1980-02-06 AU AU55269/80A patent/AU534863B2/en not_active Ceased
- 1980-02-06 IT IT8067179A patent/IT1133063B/en active
- 1980-02-07 GB GB8004104A patent/GB2042580B/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
AU534863B2 (en) | 1984-02-16 |
GB2042580B (en) | 1983-07-27 |
CH642997A5 (en) | 1984-05-15 |
DE3003766A1 (en) | 1980-08-21 |
PT70785A (en) | 1980-03-01 |
NL8000452A (en) | 1980-08-11 |
AU5526980A (en) | 1980-08-14 |
BR8000656A (en) | 1980-10-21 |
GB2042580A (en) | 1980-09-24 |
PT70785B (en) | 1981-06-11 |
FR2448568B1 (en) | 1983-06-24 |
IT8067179A0 (en) | 1980-02-06 |
IT1133063B (en) | 1986-07-09 |
FR2448568A1 (en) | 1980-09-05 |
GR68421B (en) | 1981-12-29 |
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