EP0214278A1 - Waschmittel mit enzym und glykosidoberflächenaktivem mittel - Google Patents

Waschmittel mit enzym und glykosidoberflächenaktivem mittel

Info

Publication number
EP0214278A1
EP0214278A1 EP19860902123 EP86902123A EP0214278A1 EP 0214278 A1 EP0214278 A1 EP 0214278A1 EP 19860902123 EP19860902123 EP 19860902123 EP 86902123 A EP86902123 A EP 86902123A EP 0214278 A1 EP0214278 A1 EP 0214278A1
Authority
EP
European Patent Office
Prior art keywords
detergent composition
enzyme
glycoside
weight
group
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.)
Withdrawn
Application number
EP19860902123
Other languages
English (en)
French (fr)
Inventor
Gail M. Howell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Primary Products Ingredients Americas LLC
Original Assignee
Tate and Lyle Ingredients Americas LLC
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tate and Lyle Ingredients Americas LLC filed Critical Tate and Lyle Ingredients Americas LLC
Publication of EP0214278A1 publication Critical patent/EP0214278A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase

Definitions

  • This invention relates to detergent products particularly those for laundry uses .
  • Enzymes have long been used in the detergent arts to enhance the cleaning of fabrics.
  • Specific stains 0 on soiled fabrics are particularly responsive to enzymes which cleave specific linkages in the molecules of the stain.
  • proteases and Upases are effective on stains such as blood or oils .
  • These stains are pro ⁇ tein fractions from food and fats such as are deposited
  • Polysaccharides discloses detergent products containing enzymes.
  • glycosides in detergent composi ⁇ tions are disclosed in U . S. Patent 4 ,446 ,042 issued May 1 , 1984 to Leslie. Further glycoside materials are described in Mansfield U . S. Patent 3 , 640 ,998 issued February 8, 1972. A method of manufacturing glycosides
  • a particular difficulty in working with enzymes is that when they are presented in the form of powders , there have been instances of sensitization to the enzyme in selected individuals .
  • the detergent prod ⁇ ucts containing the same be prepared in the form of a liquid thus minimizing any dust containing the enzyme.
  • liquid detergent formulations containing enzymes lead to problems in the stability in the enzyme.
  • the problem of placing the enzymes in a liquid environ ⁇ ment is that as organic materials , they are subject to bacterial growth and inactivation . It is therefore a problem to stabilize enzymes over long periods of time, particularly when they are exposed to heat which aggra- vates the enzyme stability .
  • the present invention deals with laundry detergent products in which the effect of the enzyme is enhanced by the inclusion of a glycoside surfactant.
  • a detergent composition compris- mg :
  • glycoside surfactant that improved laundry cleaning results can be obtained with enzymes.
  • protease enzymes are utilized with great effect in the present invention .
  • Other enzymes such as alcalases may also be utilized as well .
  • the glycosides with which the present in ⁇ vention are presently concerned are conveniently represented by the formula:
  • R(OG) ⁇ where R is an organic hydrophobic residue typically alkyl and having from 10 to 20 carbon atoms in the alkyl group.
  • the alkyl group may also be substituted such as
  • hydroxyl group may include an alkoxy group between the hydrophobic residue and the saccharide.
  • the preferred hydrophobic residue is a straight chain alkyl .
  • O is an oxygen atom and provides the linkage (ordinarily formed through an acetal mechanism) between the alkanol which is the basis of the alkyl group in the glycoside and the saccharide.
  • the saccharides employed herein are fructose, glucose, mannose, galactose , talose, gulose, allose , altrose, idose, arabinose, xylose, lyxose and ribose.
  • the glycoside is formed from glucose units.
  • the degree of polymerization is determined as an average value from the number represented by x .
  • the value of x which is an average varies between about 1 .2 and about 8; typically about 1.3 to about 5 and preferably about 1.4 to about 3.0.
  • the glycosides utilized herein may be prepared according to the process described in U. S. Patent 4,223,129 issued September 6, 1980 to Roth et al.
  • the source of the glycoside is not however crucial to the present invention therefore any commercial source of the glycoside may be utilized.
  • materials containing alkoxy group such as ethylene or propylene oxide pendant from the saccharide may be used. Such materials are described in pending United States patent application serial number 06/704,828 filed February 22, 1985 by Roth et al. (a copy of which is in the file of the present application).
  • the enzymes which are utilized herein are most often proteases although alcalase, lipase, tannase, and esterase may be employed in the present invention either alone or in combination with one another.
  • the enzymes utilized herein include the following materials.
  • Lipases suitable for use herein include those of animal, plant, and microbiological origin. Although only a few studies on lipase distribution in plants have been conducted, suitable lipase enzymes are present in cambium, bark, and in plant roots. In addition, lipases have been found in the seeds of fruit, oil palm, lettuce, rice, bran, barley and malt, wheat, oats and oat flour, cotton tung kernels, corn, millet, coconuts, walnuts, fusarium, cannabis and cucurbito.
  • Suitable lipases are also found in many strains of bacteria and fungi.
  • lipases suitable for use herein can be derived from Pseudomonas, Aspergillus, Pneumococcus, Staphylococcus, and Staphylococcus Toxins , Mycobacterium Tuberculosis, Mycotorula Lipolytica and Sclerotinia microorganisms.
  • Suitable animal lipases are found in the body fluids and organs of ' many species. Most organs of mammals contain lipases, but in addition , the enzymes are found in several digestive juices as well as in pancreatic juice.
  • a preferred class of animal lipase herein is the pancreatic lipase.
  • the lipases preferred for use herein " are Amano CE , Amano M-AP , Takedo 1969-4-9 , and Meito MY-30. Lipases can be employed in the present deter ⁇ gent compositions in an amount from about 0.005% to about 5% , preferably from 0. 01 % to 2.5%, " on a pure enzyme basis . While in the wash liquor , the concentra ⁇ tions employed are dependent upon the particular enzyme used and the conditions of solution , such as pH , temperature, and period of the pre-soak , if any. Normally , concentrations of enzyme in the range of from about 1 ppm to about 100 ppm , and preferably from about 5 ppm to about 500 ppm , are employed.
  • Pre-soak compositions having a lipase component within the range defined hereinbefore normally provides useful concentrations of lipase in solution.
  • the amylolytic enzymes which can be stabilized and enhanced in the detergent composition embodiment can be of fungal , plant, animal or bacterial origin. Suitable amylolytic enzymes include alpha and beta amylases.
  • suitable alpha-amylases of mold origin including those derived from Aspergillus oryzae, Aspergil lus niger, Aspergillus alliaceus , Aspergillus wentii , and Pencillium glaucum .
  • alpha- amylases derived from cereal grains , pancreatic sources and such bacteria as Bacillus subtilis , Bacillus macerans . Bacillus mesentericus and Bacillus thermophilus are also useful herein . These enzymes are active in the pH range of from about 4.5 to about 12 and , depending upon the species , at temperatures including laundering temperatures , i . e. , 35°C up to the boil .
  • Preferred amylolytic enzymes herein are the alpha-amylases derived from the bacterial organism Bacillus subtilis. These amylases provide excellent desizing and starch digestive properties and are especially useful in the laundering of textile materials containing soils and stains of a starchy nature.
  • amylolytic enzymes useful herein can be employed in a pure state. Generally, they are employed in the form of a powdered commercially available prepa ⁇ ration wherein the amylolytic enzyme is present in an amount of from about 2 to about 80% of the preparation . The remaining portion , i. e. , about 20% to about 98%, comprises inert vehicle such as sodium sulfate, calcium sulfate , sodium chloride, clay or the like.
  • the active enzyme content of these commercial enzyme compositions is the result of manufacturing methods employed and is not critical herein so long as the finished compositions of this invention have the hereinafter specified enzyme content.
  • Diasmen alpha-amylase Daiwa Kasei KK , Tokyo , Japan
  • Rapidase alpha-amylase THC-25 Rapidase, Seclin, France
  • Novo Bacterial alpha-amylase Novo Industri , Copenhagen , Denmark
  • Wal lerstein alpha-amylase Wood lerstein Company , Staten Island , New York
  • Rhozyme-33 and Rhozyme H-39 Rohm S Haas , Philadelphia , Pennsylvania
  • Preferred herein as a powdered enzyme preparation containing alpha-amylase and a mixture of alkaline and neutral proteases Preferred herein as a powdered enzyme preparation containing alpha-amylase and a mixture of alkaline and neutral proteases .
  • amylolytic enzymes can be employed in the detergent composition embodiment of this invention in an amount from about 0.005% to about 5% , preferably from 0.01 % to 2.5% on a pure enzyme basis .
  • Suitable proteolytic enzymes for use in the detergent composition embodiment can be of vegetable, animal bacterial , mold and fungal origin .
  • the proteolytic enzyme can be employed in the compositions of the present invention in an amount of 0.005% to about 5%, preferably 0.01 % to 2.5% on a pure enzyme basis. Best results in terms of overall cleaning efficacy and stain-removing properties are attained when the proteolytic enzyme is employed in an amount of about 0.01% to about 1% on a pure enzyme basis.
  • Specific examples of proteases suitable for use are trypsin, collagenase, keratinase, elastase, subtilisin, BPN and BPN 1 .
  • Preferred proteases are serine proteases produced from microorganisms such as bacteria, fungi or mold.
  • Specific examples of commercial enzyme prod ⁇ ucts and the manufacturer thereof include: Alcalase, Novo Industri, Copenhagen, Denmark; Maxatase, Koninklijke Nederlandsche Gist-En Spiritusfabriek N.V., • Delft, Netherlands; Protease B-4000 and Protease AP, Schweizerische Ferment A.G., Basel, Switzerland; CRD-Protease ' , Monsanto Company, St.
  • the glycoside surfactant as previously dis ⁇ cussed is employed in the present invention at an amount from about 1 % to about 70%; preferably from about 5% to about 65% and most preferably from about 10% to about 55% by weight of the total composition.
  • the enzymes employed herein are included in the composition at from about 0.005% to about 5%; preferably from about 0.01 % to about 5% by weight of the composition .
  • the remainder of the composition at from about 5% to about 80%; preferably from about 10% to about 75%; most pref- erably from about 20% to. about 60% by .
  • weight of the total composition is a member selected from the group consist ⁇ ing of water , lower alcohols , glycols , detergent builders and mixtures thereof.
  • the water is included herein as the preferred embodiment of the invention gives an aqueous based liquid product thereby minimizing the potential of allergic reactions to susceptible consumers .
  • the lower alcohols and glycols are respectively materials which may be utilized to thin the composition and to stabilize the enzyme within the composition .
  • propylene glycol is an excellent enzyme stabilizer and may be easily incorporated within the present invention .
  • the lower alcohols include methanol , ethanol , normal propyl , isopropyl and mixtures thereof.
  • the detergent builders which may be incor ⁇ porated within the present invention include all matter of normally utilized detergent builders such as orthophos- phates , pyrophosphates , higher polymeric phosphates such as tripolyphosphate, carbonates , citrates , organic builders including those described in pending U . S. Patent application 06/664 ,451 to Valenty filed October 23 , 1984 (equivalent to EP-A-150930) and aluminolsilicates.
  • the water soluble materials included in the foregoing description are utilized in the form of their sodium , potassium, or ammonium salts. Where the organic to water ratio content of the detergent product is particularly high , it is often preferred to utilize the potassium salts because of their enhanced solubility.
  • anionic cosurfactants are conveniently selected from the group consisting of alkyl sulfates , alkyl e ' thersulfates, olefin sulfonates. , paraffin sulfonates , alkylbenzene sulfonates , and mixtures thereof.
  • the hydrophobic portion is usually obtained from an alcohol which varies between about 10 and about 20 carbon atoms; preferably from about 12 to about 18 carbon atoms.
  • the anionic cosurfactants are conveniently formulated such that the cationic portion of the cosurfactant is selected from the group consisting of sodium , potassium or ammonium or mixtures thereof.
  • the anionic cosurfactant is typically used in an amount of from about 3% to about 40%; preferably from about 5% to about 35% by weight.
  • the present invention also allows for the inclusion of nonionic cosurfactants .
  • the nonionic cosurfactant will be an ethoxylated alcohol or an ethoxylated alkylphenyl.
  • the hydrophobic (alkyl ) portion of the nonionic cosurfactants are typically from about 10 to about 20 carbon atoms; preferably from about 12 to about 18 carbon atoms in length .
  • the amount of nonionic co-surfactant employed in the present invention is typical ly from about 5% to about 40%; pref ⁇ erably from about 7% to about 35% by weight.
  • a further variable from the present invention is the inclusion of a cationic surfactant.
  • the cationic surfactants used in the composition of the present invention are preferably those containing two long carbon chains in conjunction with a quaternary ammonium group.
  • the two long chains contain an average from about 12 to about 22 , preferably from about 16 to 22 , more preferably from about 16 to about 18 carbon atoms in each group.
  • the remaining groups if any , are attached to the " quaternary nitrogen atom are preferably a C. to C Pain alkyl or hydroxy alkyl group.
  • These chains can contain hydroxy groups or heteroatoms or other linkages , such as double or triple carbon- carbon bonds , ester , amide, or ether linkages. However , it is preferred that the long chains be alkyl groups.
  • the amount of the cationic surfactants when included in the present invention are typically at a level from about 1% to about 30%; preferably from about 2% to about 20% by weight of the total composition.
  • Suitable cationic surfactants are described in U . S. Patent 4,493 ,773 to Cook et al issued January 15 , 1985 which is incorporated herein by reference.
  • the detergent composition of the present invention are typically used at a solids concentration in the wash liquor at from about 0.01 % to about 1 .0% by weight.
  • the lower percentage of use for the product is typical in American washes which are done on a dilute basis while the higher surfactant concentrations are typical of the European boil wash systems.
  • Other laundry additives may also be included in the composi ⁇ tions described herein such as optical brighteners , dyes , bleaches and the like.
  • the product is preferably a pourable liquid but may be formulated as a granule or other solid form.
  • a surfactant product is prepared according to the present invention by introducing a protease (alcalase 2.5L from NOVO) at a level of 1 part with an alkylpolyglucoside (alkyl 12-13 carbons) having an average DP of 3.0 at 32 parts together with 67 parts of water.
  • This product is found to clean clothes effec ⁇ tively when used at a wash concentration level of the surfactant present at 0. 15% by weight in water under wash conditions of 37°C .
  • EXAMPLE 11 A series of comparative examples is run show- ing the effect of the alkylpolyglycoside in enhancing the effectiveness of the enzyme utilized in a laundry deter ⁇ gent product.
  • APG is an alkyl polyglucoside with a hydrophobic portion of the molecule is between 12 and 13 carbon atoms long and the DP of the product is 3.
  • LAE is a linear alcohol ethoxylate having an average degree of ethoxylation of 7 and a carbon atom chain length of between 12 and 15 carbon atoms ( NEODOL 25-7 from Shell )
  • LAES is a linear alcohol ethoxysulfate sodium salt where the number of ethoxy units is 3 and the carbon chain length of the surfactant is 12 to 15 carbons (NEODOL 25-35) .
  • LAS is an alkyl benzene sulfonate sodium salt wherein the alkyl portion is 12 carbon atoms.
  • the ratios shown are by weight of the respec ⁇ tive ingredients.
  • the first column of Table I I shows the surfactant without the enzyme present whereas the second column shows the added cleaning power of the enzyme.
  • the last column shows the units of cleaning due to the enzyme.

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)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Detergent Compositions (AREA)
EP19860902123 1985-03-07 1986-03-04 Waschmittel mit enzym und glykosidoberflächenaktivem mittel Withdrawn EP0214278A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US70899485A 1985-03-07 1985-03-07
US708994 2000-11-08

Publications (1)

Publication Number Publication Date
EP0214278A1 true EP0214278A1 (de) 1987-03-18

Family

ID=24848044

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19860902123 Withdrawn EP0214278A1 (de) 1985-03-07 1986-03-04 Waschmittel mit enzym und glykosidoberflächenaktivem mittel

Country Status (3)

Country Link
EP (1) EP0214278A1 (de)
ES (1) ES8708008A1 (de)
WO (1) WO1986005187A1 (de)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2245000B (en) * 1987-09-17 1992-06-03 Colgate Palmolive Co Liquid detergent composition
GB8726999D0 (en) * 1987-11-18 1987-12-23 Unilever Plc Enzymatic liquid detergent composition
DE4029035A1 (de) * 1990-09-13 1992-03-19 Huels Chemische Werke Ag Waschmittel
DE4034840A1 (de) * 1990-11-02 1992-05-07 Henkel Kgaa Enzymatisches fluessigwaschmittel
CA2088230A1 (en) * 1992-02-03 1993-08-04 James Gordon Detergent composition
EP0838518B1 (de) * 1992-09-11 2002-11-13 Cognis Deutschland GmbH & Co. KG Detergensgemische
DE4315854A1 (de) * 1993-05-12 1994-11-17 Henkel Kgaa Lipasehaltige Wasch- und Reinigungsmittel
DE4339382A1 (de) * 1993-11-18 1995-05-24 Henkel Kgaa Enzymkombinationhaltige flüssige Wasch- und Reinigungsmittel
AU2293595A (en) * 1994-04-22 1995-11-16 Procter & Gamble Company, The Amylase-containing detergent compositions
US5783546A (en) * 1994-04-22 1998-07-21 Procter & Gamble Company Amylase-containing detergent compositions
DE19748396A1 (de) * 1997-11-03 1999-05-06 Henkel Kgaa Verfahren zur Entfernung hydrophober Verunreinigungen mittels spaltbarer nichtionischer Tenside
US6989352B2 (en) * 2002-06-12 2006-01-24 Halliburton Energy Services, Inc. Silicic acid mud lubricants
ITVA20030019A1 (it) * 2003-06-13 2004-12-14 Lamberti Spa Detergenti liquidi acquosi a base di esteri anionici di alchilpoliglicosidi.
FR2959140A1 (fr) * 2010-04-23 2011-10-28 Agro Ind Rech S Et Dev Ard Preparations facilitees de vesicules a l'aide des poly-pentosides d'alkyles et utilisations desdites preparations
WO2023096523A1 (ru) * 2021-11-24 2023-06-01 "Скайлаб Аг" Биоразлагаемая моющая композиция на основе липазы

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3519570A (en) * 1966-04-25 1970-07-07 Procter & Gamble Enzyme - containing detergent compositions and a process for conglutination of enzymes and detergent compositions
US4483780A (en) * 1982-04-26 1984-11-20 The Procter & Gamble Company Detergent compositions containing polyglycoside and polyethoxylate detergent surfactants
US4493773A (en) * 1982-05-10 1985-01-15 The Procter & Gamble Company Low phosphate, softening laundry detergent containing ethoxylated nonionic, alkylpolysaccharide and cationic surfactants

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO8605187A1 *

Also Published As

Publication number Publication date
WO1986005187A1 (en) 1986-09-12
ES8708008A1 (es) 1987-09-16
ES552727A0 (es) 1987-09-16

Similar Documents

Publication Publication Date Title
US4011169A (en) Stabilization and enhancement of enzymatic activity
US3944470A (en) Stabilization and enhancement of enzymatic activity
WO1986005187A1 (en) Detergent composition containing an enzyme and a glycoside surfactant
TW419523B (en) Liquefying alkaline <alpha>-amulases, preparation process thereof and detergent compositions containing the same
US6060441A (en) Cleaning compositions having enhanced enzyme activity
US4421664A (en) Compatible enzyme and oxidant bleaches containing cleaning composition
Bhange et al. Simultaneous production of detergent stable keratinolytic protease, amylase and biosurfactant by Bacillus subtilis PF1 using agro industrial waste
US5078898A (en) Detergent compositions comprising pseudomonas lipase and a specific protease
EP2596089B1 (de) Waschmittelzusammensetzungen mit einem Biotensid und Lipase
EP1000136B1 (de) Glucanasehaltiges reinigungsmittel für harte oberflächen
EP0399681B1 (de) Wäschewaschverfahren
WO1991010723A1 (en) Bacteriolytic enzyme native to a nocardiopsis strain, its production and use.
AU687536B2 (en) Stable enzyme-containing aqueous laundry prespotting composition
JP3641108B2 (ja) 自動食器洗浄機用洗浄剤組成物
US5223169A (en) Hydrolase surfactant systems and their use in laundering
Aehle Development of new amylases
Tanaka et al. Study on the substrate specificity of α-amylases that contribute to soil removal in detergents
AU772325B2 (en) Laundry detergent composition containing high level of protease enzyme
Sizaire et al. Enzyme stability with essential oils and surfactants. Growing towards green disinfectant detergents
Niyonzima et al. Detergent-compatible amylases produced by fungal species and their applications in detergent industry
JP2009052006A (ja) 酵素含有洗浄剤組成物
JPH0699715B2 (ja) 自動食器洗浄機用洗浄剤組成物
JP3403255B2 (ja) 洗浄剤組成物
Fernandes 9 Role of microbial oxidative enzymes
JPH08508775A (ja) 酵素洗剤

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: A1

Designated state(s): BE DE FR GB IT NL SE

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 19861209

RIN1 Information on inventor provided before grant (corrected)

Inventor name: HOWELL, GAIL, M.