AU619892B2 - Detergent compositions - Google Patents
Detergent compositions Download PDFInfo
- Publication number
- AU619892B2 AU619892B2 AU41080/89A AU4108089A AU619892B2 AU 619892 B2 AU619892 B2 AU 619892B2 AU 41080/89 A AU41080/89 A AU 41080/89A AU 4108089 A AU4108089 A AU 4108089A AU 619892 B2 AU619892 B2 AU 619892B2
- Authority
- AU
- Australia
- Prior art keywords
- detergent composition
- weight
- nonionic surfactant
- surfactant system
- 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.)
- Ceased
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Classifications
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- 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
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0036—Soil deposition preventing compositions; Antiredeposition agents
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- 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
- C11D3/37—Polymers
- C11D3/3788—Graft polymers
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
-S
AUSTRALIA
PATENTS ACT 1952 COMPLETE SPECIFICATION Form
(ORIGINAL)
FOR OFFICE USE Short Title: Int. Cl: Application Number: Lodged: Complete Specification-Lodged: Accepted: Lapsed: Published: t IS Priority: Related Art: TO BE COMPLETED BY APPLICANT Name of Applicant: Address of Applicant:
I'
C C I C C I CC CCC C UNILEVER PLC UNILEVER HOUSE
BLACKFRIARS
LONDON EC4
ENGLAND
Actual Inventor: Address for Service: GRIFFITH HACK CO., 601 St. Kilda Road, Melbourne, Victoria 3004, Australia.
Complete Specification for the invention entitled: DETERGENT COMPOSITIONS.
The following statement is a full description of this invention including th'; best method of performing it known to me:i i 1- C.3266 DETERGENT COMPOSITIONS I *i TECHNICAL FIELD The present invention relates to fabric washing detergent compositions having improved antiredeposition properties.
BACKGROUND AND PRIOR ART Redeposition of soil removed from washed articles back onto the articles themselves is a well-known problem which is of particular significance with textile fabrics, and many solutions to this problem have been suggested.
Classically, sodium carboxymethyl cellulose was incorporated into fabric washing compositions, and that compound is still used today. More recently, copolymers of ethylene or vinyl methyl ether and maleic anhydride, copolymers of acrylic acid and maleic anhydride, and homopolymers of acrylic acid have been suggested in the patent literature; see, for example, GB 1 269 848 (Procter Gamble) and GB 1 460 893 (Unilever).
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2 C.3266 Another polymeric material that has been suggested for improving soil suspension is polyvinylpyrrolidone.
EP 262 897A (Unilever) discloses detergent compositions containing polyvinylpyrrolidone, an anionic surfactant, and a nonionic surfactant system having a hydrophilic-lipophilic balance (HLB) of not more than 10.5.
EP 219 048A (BASF) discloses the use of graft copolymers of polyalkylene oxide with vinyl acetate as greying inhibitors in the washing and post-wash treatment of synthetic textile fabrics.
We have now discovered that detergent compositions containing a graft copolymer of this type in conjunction with a 3ow-HLB nonionic surfactant system exhibit surprisingly enhanced soil suspension (antiredeposition) properties on polyester/cotton fabrics.
ito 00 o o o 0 r2 I- 3 C.3266 DEFINITION OF THE INVENTION The present invention provides a detergent composition comprising: from 2 to 50% by weight of a detergent active system which amount includes at least 2% by weight of a nonionic surfactant system consisting of one or more nonionic surfactants, the nonionic surfactant system having a cloud 10 point (as hereinbefore defined) not higher than 400C when in distilled water at a concentration of and 0 00 oso* from 0.1 to 3% by weight of a graft copolymer S of polyethylene oxide, polypropylene oxide or polybutylene oxide *00000 S with (ii) vinyl acetate (optionally partially saponified) 0e 15 in a weight ratio of to-(ii) of from 1:0.2 to 1:10.
DETAILED DESCRIPTION OF THE INVENTION 0 00 0o The present invention relates to detergent o compositions containing two specified ingredients a nonionic surfactant system, and a graft copolymer 0 0 which may additionally contain any other conventional detergent ingredients, for example, other surfactants, builders, bleach systems, antifoam systems, fluorescers, inorganic salts, and other materials well known to those skilled in formulating detergents. The compositions of the invention may take any suitable form, for example, powders, liquids or bars.
4 C.3266 The nonionic surfactant system The nonionic surfactant system of the present invention exists as a cloudy phase somewhere in the temperature range of 0 0 C to 40 0 C, preferably 0°C to in distilled water at a concentration of In practice this means that the system has a cloud point of not more than 40 C, preferably not more than 15 C.
Cloud point is a term well known in the art, for example, from "Surface Active Ethylene Oxide Adducts" by N Schonfeldt, Pergamon Press 1969, pages 145 to 154. In general terms the cloud point of a surfactant material is S the temperature at which association between the o surfactant molecules and water molecules through hydrogen S. o 15 bonding breaks down, leading to the separation of surfactant-rich and water-rich phases and a consequent 0. increase in turbidity or cloudiness.
*000 000 The cloud point correlates approximately to the i 20 hydrophilic-lipophilic balance (HLB) of the surfactant i system and it is therefore preferred that the HLB should be not higher than 10.5 and more preferably not higher i than 9.5. The HLB should however preferably be above ij 6.0, more preferably above 8.0, in order to provide sufficient detergency.
I Suitable nonionic detergent compounds which may be used include in particular the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
Specific nonionic detergent compounds are alkyl (C6- 22 phenol-ethylene oxide condensates, the condensation L A 5 C.3266 products of linear or branched aliphatic C 8 20 primary or secondary alcohols with ethylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine. Other so-called nonionic detergent compounds include long-chain tertiary amine oxides, tertiary phosphine oxides, and dialkyl sulphoxides.
Where, for example, alkylene oxide adducts of fatty materials (aliphatic alcohols, acids or amides) are used as the nonionic detergent compounds, the number of alkylene oxide groups per molecule has a considerable effect upon the cloud point as indicated by the °o0o Schonfeldt reference mentioned above. The chain length 15 and nature of the fatty material is also influential, and 41 thus the preferred number of alkylene oxide groups per molecule depends on the the nature and chain length of S, the fatty material. We have found, for example, that where the fatty material is an alcohol having about 12 to 15 carbon atoms, the adducts having 3 and 4 ethylene oxide groups per molecule (hereinafter the 3EO and 4EO materials) both have cloud points of less than 0 C and are therefore suitable for use in the present invention.
The corresponding 5EO and 6EO surfactants have cloud points of about 12°C and about 30°C respectively; both are therefore suitable for use in the present invention, Sbut the 5EO is preferred to the 6EO.
The corresponding 7EO surfactant has a cloud point $30 of about 48°C and is therefore unsuitable for use in the present invention, unless in admixture with another surfactant of lower cloud point: for example, a mixture of 1 part by weight of the 7EO material with 3 parts by -6 C.3266 weight of the 3EO material has a sufficiently low cloud point to be useful in the present invention. Further jl ethoxylation raises the cloud point still higher: thus !ji the corresponding 11EO material has a cloud point higher than 80 C and is unsuitable for use in the present !i invention.
Thus preferred nonionic surfactants for use in the compositions of the invention are C 12 1 5 aliphatic alcohols having a degree of ethoxylation not exceeding 6, preferably 3 to o oa S ooo The nonionic surfactant system of the compositions of the invention may consist of a single nonionic S° 15 surfactant of appropriate cloud point, although it must .0.4 be remembered that even a single commercial nonionic surfactant is a mixture of materials of different chain (I lengths and degrees of ethoxylation: the chain lengths and degrees of ethoxylation quoted in this specification i 20 are average values. Alternatively, a nonionic l surfactant system of suitable cloud point and HLB value may be obtained by blending two or more nonionic surfactants, as exemplified by the 7EO/3EO mixture mentioned in the previous paragraph.
The nonionic surfactant system is preferably present Sin an amount of from 2 to 20% by weight, more preferably from 3 to 10% by weight, based on the total composition.
S As indicated below under "Optional Ingredients", other surfactants, of other ionic types, may also be present if desired, the total amount of surfactant of all ionic types present being within the range of from 2 to 50% by weight, preferably from 5 to 40% by weight, of the final composition.
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7 C.3266 The graft copolymer The graft copolymers used in the compositions of the present invention are described and claimed in EP 219 048A (BASF). They are obtainable by grafting a polyalkylene oxide of molecular weight (number average) 2000 100 000 with vinyl acetate, which may be partially saponified, in a weight ratio of polyalkylene oxide to vinyl acetate of 1:0.2 to 1:10. The vinyl [i 10 acetate may, for example, be saponified to an extent of rc up to 15%. The polyalkylene oxide may contain units of jethylene oxide, propylene oxide and/or butylene oxide; polyethylene oxide is preferred.
0 0 o, 0 15 Preferably the polyalkylene oxide has a S, number-average molecular weight of from 4000 to 50 000, and the weight ratio of polyalkylene oxide to vinyl acetate is from 1:0.5 to 1:6. Especially preferred are i; polymers derived from polyethylene oxide of molecular i 20 weight 2000-50 000 and having a weight ratio of j polyethylene oxide to vinyl acetate of from 1:0.5 to 1:6.
A material within this definition, based on j polyethylene oxide of molecular weight 6000 (equivalent i to 136 ethylene oxide units), containing approximately l 3 parts by weight of vinyl acetate units per 1 part by |weight of polyethylene oxide, and having itself a molecular weight of 24 000, is commercially available from BASF as Sokalan (Trade Mark) HP22.
The polymers are present in the compositions of the invention in amounts of from 0.1 to 3% by weight, preferably from 0.3 to 1% by weight.
8 C.3266 i Optional ingredients As well as the specified nonionic surfactant system I and graft copolymer, the compositions of the invention i 5 may contain any other non-interfering ingredients known i to be suitable for incorporation into detergent ij compositions.
ii The compositions may usefully contain one or more soap or non-soap anionic, cationic, amphoteric or H zwitterionic surfactants, or combinations of these.
Many suitable detergent-active compounds are available "and are fully described in the literature, for example, Sin "Surface-Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
The preferred detergent-active compounds that can be used, in addition to the specified nonionic surfactant system, are soaps and synthetic non-soap anionic i 20 surfactants.
Synthetic anionic surfactants are well known to those skilled in the art. Examples include alkylbenzene sulphonates, particularly sodium linear alkylbenzene sulphonates having an alkyl chain length of C primary and secondary alkyl sulphates, particularly |l sodium C 12
-C
15 primary alcohol sulphates; olefin i sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
It may also be desirable to include one or more soaps of fatty acids. These are preferably sodium soaps derived from naturally occurring fatty acids, for example, the fatty acids from coconut oil, beef tallow, sunflower or hardened rape seed oil.
9 C.3266 A preferred type of detergent composition suitable for use in most automatic fabric washing machines contains anionic and nonionic surfactant together in a weight ratio of at least 0.67:1, preferably at least 1:1, and more preferably within the range of from 1:1 to 10:1.
Soap may also be present if desired.
As previously indicated, the total amount of surfactant in the compositions of the invention is from 2 to 50% by weight, and is preferably from 5 to 40% by weight.
0 ee Compositions of the invention will also generally 0 00 c O° contain one or more detergency builders. These are as 15 well known to the skilled formulator as are the o surfactants listed above. Inorganic builders that may .o o be present include alkali metal (generally sodium) 000 ortho-, pyro- and tripolyphosphate, carbonate, and crystalline and amorphous aluminosilicates; while organic builders include polycarboxylate polymers such as 0oo0. polyacrylates, acrylic/maleic copolymers, and polyacetal 0: a carboxylates, and monomeric polycarboxylates such as o nitrilotriacetates, citrates and carboxymethyloxysuccinates. This list is not intended to be exhaustive. The total level of detergency builder is generally within the range of from 20 to 80% by weight.
According to a preferred embodiment of the invention, the compositions contain less than 10% by weight of inorganic phosphate builders, and are more preferably substantially free of inorganic phosphate.
10 C.3266 In this preferred embodiment, the builder system preferably comprises crystalline or amorphous alkali metal aluminosilicate, optionally in conjunction with a supplementary builder. The aluminosilicate is suitably present in an amount of from 10 to 60% by weight.
Detergent compositions according to the invention i may also suitably contain a bleach system. Preferred are peroxy bleach compounds, for example, inorganic persalts or organic peroxyacids, which may be employed in Si conjunction with activators to improve bleaching action Oct at low wash temperatures. The skilled detergent worker *ec will have no difficulty in applying the normal principles i c S* to choose a suitable bleach system.
t i Other materials that may be present in detergent 1 i ,.to compositions of the invention include sodium silicate, c fluorescers, inorganic salts such as sodium sulphate, ~I enzymes, lather control agents or lather boosters as 20 appropriate, pigments, and perfumes. Again, this list lec is not intended to be exhaustive.
C i i Preparation of detergent compositions Detergent compositions of the invention may be prepared by any suitable method. Detergent powders are suitably prepared by spray-drying a slurry of compatible heat-insensitive components, and then spraying on or postdosing those ingredients unsuitable for processing via the slurry. The skilled detergent formulator will generally have no difficulty in deciding which components should be included in the slurry and which should be postdosed or sprayed on.
11 C.3266 The graft copolymer is available as a solution having a solids content of 20% which is stable at slurry processing temperatures and can be incorporated in the slurry without problems, provided that the pH is maintained below 12.
The nonionic surfactant system is preferably not incorporated via the slurry. If, however, a mixed system is used which includes a relatively highly ethoxylated component, that component may if desired be processed via the slurry while material of lower ethoxylation is sprayed on or postdosed on a solid ,00, carrier.
c 15 The invention is further illustrated by the j following non-limiting Examples, in which parts and percentages are by weight unless otherwise stated.
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ii i ii i
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I 12 C.3266
EXAMPLES
Example 1 Four detergent compositions were prepared to the following formulation by conventional slurry-making, spray-drying and postdosing techniques: S 0 0 0 oooo o oo i oooo 0 0 0 0 0 0 0 000000 S 0 0 0 0 000 Sodium linear alkylbenzene sulphonate Nonionic surfactant (see below) Zeolite 4A (hydrated basis) 15 Sodium alkaline silicate Sodium sulphate Sodium carbonate Sodium carboxymethylcellulose Fluorescer Sodium perborate monohydrate Tetraacetylethylenediamine (76% granules) Enzyme granules Graft copolymer (Sokalan HP22) Water and minor ingredients 24.0 19.3 0.7 0 or to 100.0 I C The compositions prepared contained the following amounts of nonionic surfactants and Sokalan HP22: v- tmrr.. .l 13 C.3266 Example 1 A B C Nonionic surfactant 7EO 1 1.0 4.0 4.0 2 Nonionic surfactant 3EO 3.0 Sokalan HP22 0.5 1 Synperonic (Trade Mark) A7 ex ICI, C 12 linear primary alcohol 7EO 2 Synperonic (Trade Mark) A3 ex ICI, C2_ 0 0 12-15 ,0 linear primary alcohol 3EO oe 0 15 It will be seen that Composition 1 illustrates the invention while Compositions A to C are comparative.
o 0 fog The soil suspension (antiredeposition) properties of the four compositions were compared by means of the following procedure. Two new, clean, unwashed polyester/cotton test cloths were washed together with five soiled cloths in a tergotometer at 60°C in 500 (French) hard water (Ca:Mg ratio 4:1) at a liquor to I cloth ratio of about 50:1, the wash liquor containing 4 g/1 of the detergent composition under test. The soiled cloths carried a range of different soils such as clay, oil, fat, proteinaceous, and ink. The wash cycle was repeated a further nine times, the soiled cloths being -replaced by new soiled cloths (with the same range of soils) for each wash cycle.
I
a~ 7 14 C.3266 The reflectance of the two new cloths was measured before washing, and after the tenth wash cycle. The reduction in reflectance of the washed fabrics after ten washes is shown in the following table; the lower the reduction in reflectance, the less redeposition had occurred.
Example 1 A 0000 i oooo 0 0 0 ao o oo 0 0 S0o 0 0000 Delta R60* -2.4 -5.6 -7.5 -4.7 a ij i i a 'i i i i i 1 oe 0a t 0 0 c* S C 0 C
SC
I CC
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Claims (3)
1. A detergent composition comprising: from 2 to 50% by weight of a detergent active system which amount includes at least 2% by weight of a nonionic surfactant system consisting of one or more nonionic surfactants, the nonionic surfactant system having a cloud point (as hereinbefore defined) not higher than 40 0 C when in distilled water at a concentration of and oa from 0.1 to 3% by weight of a graft copolymer of polyethylene oxide, polypropylene oxide or polybutylene oxide with (ii) vinyl acetate (optionally partially saponified) in a weight ratio of to (ii) of from 1:0.2 to 1:10. SA0 0000
2. A detergent composition as claimed in claim 1, Swherein the nonionic surfactant system has a cloud point not higher than 150 C
43. A detergent composition as claimed in claim 1 or claim 2, wherein the nonionic surfactant system has an HLB value not greater than I_ plCI~CI~---UII. X- 16 C.3266GB A detergent composition as claimed in any preceding claim, wherein the nonionic surfactant system consists of one or more C 12 15 aliphatic alcohols ethoxylated with an average of not more than 5 moles of ethylene oxide. 6. A detergent composition as claimed in claim wherein the nonionic surfactant system consists of one or more C 12 1 5 aliphatic alcohols ethoxylated with an average of 3-4 moles of ethylene oxide. i o o o i o0oo .ooooO 0 S ooo 0000o 0000 7. A detergent composition as claimed in any preceding claim, wherein the nonionic surfactant system is present in an amount of from 2 to 20% by weight. 8. A detergent composition as claimed in claim 7, wherein the nonionic surfactant system is present in an amount of from 3 to 10% by weight. i i r i i i ji t 'i i! 0 0 6 66 9. A detergent composition as claimed in any preceding claim, wherein the graft copolymer isb-~tainabl by grafting a polyalkylene oxide of molecular weight (number 25 average) 2000 100 000 with vinyl acetate (optionally partially saponified) in a weight ratio of polyalkylene oxide to vinyl acetate of 1:0.2 to 1:10. rii ii '1 17 C.3266GB A detergent composition as claimed in. any preceding claim, wherein the graft copolymer is ta4inalc by grafting a polyalkylene oxide of molecular weight (number average) 4000 50 000 with vinyl acetate (optionally partially saponified) in a weight ratio of polyalkylene oxide to vinyl acetate of 1:0.5 to 1:6. 0 9 .0 00 ,t o oo 0o o 0 0o 0 0 0 00oo o 11. A detergent composition as claimed in any one of claims 1 to 9, wherein the graft copolymer isb~tainahl by grafting a polyethylene oxide of molecular weight (number average) 2000 50 000 with vinyl acetate (optionally partially saponified) in a weight ratio of polyethylene oxide to vinyl acetate of 1:0.5 to 1:6. 12. A detergent composition as claimed in any preceding claim, wherein the graft copolymer is present in an amount of from 0.3 to 1.0% by weight. 0000 0 0 0 o a S OI L r 13. A detergent composition as claimed in any preceding claim, which further comprises from 10 to 60% by weight of crystalline or amorphous alkali metal aluminosilicate. Ir~LL, II.j1j 14. A detergent composition as claimed in any preceding claim, which further comprises one or more anionic surfactants. P- i i A 4 t 18 C.3266GB A detergent composition as claimed in any preceding claim, which contains less than 10% by weight of inorganic phosphate builder. 16. A detergent composition as claimed in claim which is suLb tdti-al- free of inorganic phosphate builders. Ott oI o re I C tots DATED THIS 6TH DAY OF SEPTEMBER 1989 UNILEVER PLC By its Patent Attorneys: GRIFFITH HACK CO. Fellows Institute of Patent Attorneys of Australia os D t
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8821035 | 1988-09-07 | ||
GB888821035A GB8821035D0 (en) | 1988-09-07 | 1988-09-07 | Detergent compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
AU4108089A AU4108089A (en) | 1990-03-15 |
AU619892B2 true AU619892B2 (en) | 1992-02-06 |
Family
ID=10643230
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU41080/89A Ceased AU619892B2 (en) | 1988-09-07 | 1989-09-06 | Detergent compositions |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0358474B1 (en) |
JP (1) | JPH02117999A (en) |
AU (1) | AU619892B2 (en) |
BR (1) | BR8904489A (en) |
CA (1) | CA1328065C (en) |
DE (1) | DE68919392T2 (en) |
ES (1) | ES2063139T3 (en) |
GB (1) | GB8821035D0 (en) |
NO (1) | NO172854C (en) |
ZA (1) | ZA896841B (en) |
Families Citing this family (26)
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US5266166A (en) * | 1992-05-18 | 1993-11-30 | Betz Paperchem, Inc. | Methods for controlling the deposition of organic contaminants in pulp and papermaking processes using a polyalkylene oxide/vinyl acetate graft copolymer |
ATE188991T1 (en) * | 1993-09-13 | 2000-02-15 | Procter & Gamble | GRANULAR DETERGENT COMPOSITIONS WITH NON-IONIC SURFACTANT AND METHOD FOR THE PRODUCTION THEREOF |
US5698510A (en) * | 1993-09-13 | 1997-12-16 | The Procter & Gamble Company | Process for making granular detergent compositions comprising nonionic surfactant |
GB9403155D0 (en) * | 1994-02-18 | 1994-04-06 | Unilever Plc | Detergent compositions |
DE4424818A1 (en) * | 1994-07-14 | 1996-01-18 | Basf Ag | Low-viscosity mixtures of amphiphilic nonionic graft copolymers and viscosity-reducing additives |
US5728672A (en) * | 1995-08-04 | 1998-03-17 | Reckitt & Colman Inc. | Pine oil hard surface cleaning compositions |
GB2304115B (en) * | 1995-08-04 | 1999-08-25 | Reckitt & Colman Inc | Pine oil hard surface cleaning compositions |
WO1997009415A1 (en) * | 1995-09-04 | 1997-03-13 | Unilever Plc | Detergent compositions and process for preparing them |
EP0778340A3 (en) | 1995-12-06 | 1999-10-27 | Basf Corporation | Improved non-phosphate machine dishwashing compositions containing copolymers of alkylene oxide adducts of allyl alcohol and acrylic acid |
US5750483A (en) | 1995-12-06 | 1998-05-12 | Basf Corporation | Non-phosphate machine dishwashing compositions containing polycarboxylate polymers and nonionic graft copolymers of vinyl acetate and polyalkylene oxide |
US6083488A (en) * | 1996-12-04 | 2000-07-04 | The Block Drug Company | Barrier to plaque formation |
JP3325830B2 (en) * | 1998-03-30 | 2002-09-17 | 株式会社日本触媒 | Bleach composition |
JP2002003890A (en) * | 2000-06-20 | 2002-01-09 | Kao Corp | Detergent composition |
CN101084298A (en) | 2004-12-17 | 2007-12-05 | 宝洁公司 | Hydrophilically modified polyols for improved hydrophobic soil cleaning |
CA2590434A1 (en) | 2004-12-17 | 2006-06-22 | The Procter & Gamble Company | Hydrophobically modified polyols for improved hydrophobic soil cleaning |
US7465701B2 (en) | 2006-05-31 | 2008-12-16 | The Procter & Gamble Company | Detergent composition |
MX2008014819A (en) | 2006-05-31 | 2008-12-01 | Basf Se | Amphiphilic graft polymers based on polyalkylene oxides and vinyl esters. |
BRPI0813289A2 (en) | 2007-06-29 | 2014-12-30 | Procter & Gamble | DETERGENT COMPOSITIONS FOR WASHING CLOTHES UNDERSTANDING POLYCHYLENE OXIDE-BASED GENTLE POLYMERS AND VINYL ESTERS. |
JP4933487B2 (en) * | 2008-05-21 | 2012-05-16 | 旭洋造船株式会社 | Fuel efficient transport ship |
JP4873388B2 (en) * | 2008-07-28 | 2012-02-08 | 上野 康男 | Starting device |
US20110152161A1 (en) * | 2009-12-18 | 2011-06-23 | Rohan Govind Murkunde | Granular detergent compositions comprising amphiphilic graft copolymers |
US8334250B2 (en) * | 2009-12-18 | 2012-12-18 | The Procter & Gamble Company | Method of making granular detergent compositions comprising amphiphilic graft copolymers |
JP2015518059A (en) | 2012-03-09 | 2015-06-25 | ザ プロクター アンド ギャンブルカンパニー | Detergent composition comprising graft polymer with broad polarity distribution |
EP2832843B1 (en) | 2013-07-30 | 2019-08-21 | The Procter & Gamble Company | Method of making granular detergent compositions comprising polymers |
EP2832842B1 (en) | 2013-07-30 | 2018-12-19 | The Procter & Gamble Company | Method of making granular detergent compositions comprising surfactants |
EP2899259A1 (en) * | 2014-01-22 | 2015-07-29 | The Procter and Gamble Company | Detergent compositions |
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US4746456A (en) * | 1985-10-12 | 1988-05-24 | Basf Aktiengesellschaft | Detergents containing graft copolymers of polyalkylene oxides and vinyl acetate as antiredeposition inhibitors |
AU4107989A (en) * | 1988-09-07 | 1990-03-15 | Unilever Plc | Detergent compositions |
AU4107889A (en) * | 1988-09-07 | 1990-03-15 | Unilever Plc | Detergent compositions |
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---|---|---|---|---|
EP0002084A1 (en) * | 1977-11-17 | 1979-05-30 | THE PROCTER & GAMBLE COMPANY | Granular detergent compositions for improved greasy soil removal |
GB8623586D0 (en) * | 1986-10-01 | 1986-11-05 | Unilever Plc | Detergent composition |
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1988
- 1988-09-07 GB GB888821035A patent/GB8821035D0/en active Pending
-
1989
- 1989-08-31 CA CA000609975A patent/CA1328065C/en not_active Expired - Fee Related
- 1989-09-04 NO NO893535A patent/NO172854C/en unknown
- 1989-09-06 ES ES89309010T patent/ES2063139T3/en not_active Expired - Lifetime
- 1989-09-06 BR BR898904489A patent/BR8904489A/en not_active Application Discontinuation
- 1989-09-06 AU AU41080/89A patent/AU619892B2/en not_active Ceased
- 1989-09-06 EP EP89309010A patent/EP0358474B1/en not_active Expired - Lifetime
- 1989-09-06 DE DE68919392T patent/DE68919392T2/en not_active Expired - Fee Related
- 1989-09-06 JP JP1231337A patent/JPH02117999A/en active Pending
- 1989-09-07 ZA ZA896841A patent/ZA896841B/en unknown
Patent Citations (3)
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---|---|---|---|---|
US4746456A (en) * | 1985-10-12 | 1988-05-24 | Basf Aktiengesellschaft | Detergents containing graft copolymers of polyalkylene oxides and vinyl acetate as antiredeposition inhibitors |
AU4107989A (en) * | 1988-09-07 | 1990-03-15 | Unilever Plc | Detergent compositions |
AU4107889A (en) * | 1988-09-07 | 1990-03-15 | Unilever Plc | Detergent compositions |
Also Published As
Publication number | Publication date |
---|---|
NO893535D0 (en) | 1989-09-04 |
NO172854C (en) | 1993-09-15 |
NO893535L (en) | 1990-03-08 |
BR8904489A (en) | 1990-04-24 |
NO172854B (en) | 1993-06-07 |
EP0358474B1 (en) | 1994-11-17 |
CA1328065C (en) | 1994-03-29 |
JPH02117999A (en) | 1990-05-02 |
ZA896841B (en) | 1991-05-29 |
EP0358474A3 (en) | 1990-10-10 |
ES2063139T3 (en) | 1995-01-01 |
GB8821035D0 (en) | 1988-10-05 |
DE68919392T2 (en) | 1995-03-30 |
DE68919392D1 (en) | 1994-12-22 |
EP0358474A2 (en) | 1990-03-14 |
AU4108089A (en) | 1990-03-15 |
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Legal Events
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MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |