EP0150872B2 - Liquid detergent compositions containing organo-functional polysiloxanes - Google Patents

Liquid detergent compositions containing organo-functional polysiloxanes Download PDF

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Publication number
EP0150872B2
EP0150872B2 EP85200027A EP85200027A EP0150872B2 EP 0150872 B2 EP0150872 B2 EP 0150872B2 EP 85200027 A EP85200027 A EP 85200027A EP 85200027 A EP85200027 A EP 85200027A EP 0150872 B2 EP0150872 B2 EP 0150872B2
Authority
EP
European Patent Office
Prior art keywords
alkyl
siloxane
polydimethylsiloxane
composition
anionic
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 - Lifetime
Application number
EP85200027A
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German (de)
English (en)
French (fr)
Other versions
EP0150872A1 (en
EP0150872B1 (en
Inventor
Christian Roland Barrat
Alfred Busch
Kosmas Sardelis
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.)
Procter and Gamble European Technical Center
Procter and Gamble Co
Original Assignee
Procter and Gamble European Technical Center
Procter and Gamble Co
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
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Application filed by Procter and Gamble European Technical Center, Procter and Gamble Co filed Critical Procter and Gamble European Technical Center
Priority to AT85200027T priority Critical patent/ATE51892T1/de
Publication of EP0150872A1 publication Critical patent/EP0150872A1/en
Publication of EP0150872B1 publication Critical patent/EP0150872B1/en
Application granted granted Critical
Publication of EP0150872B2 publication Critical patent/EP0150872B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3742Nitrogen containing silicones
    • 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
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones

Definitions

  • compositions herein comprise conventional ingredients inclusive of surface-active agents, liquid carrier and optional ingredients such as detergent builders, enzymes and side regulants and low levels of organo-functional polydi-short alkylsiloxanes.
  • the latter ingredient unexpectedly provides desirable through-the-wash textile benefits inclusive of softness.
  • the preferred siloxanes embrace amino derivatives.
  • the essential siloxanes are further characterized by a degree of substitution in the range from 0.01-0.7.
  • liquid compositions herein can be divided arbitrarily in (mostly P-)-built compositions and in substantially unbuilt compositions. Both kinds of compositions will procure textile handling benefits. Selective preference can originate from the combined use of anionic surface-active agents in combination with the subject siloxanes.
  • silicones/polydialkylsiloxanes are crowded and diverse.
  • the like siloxanes have, for example, found widespread commercial application in a detergent suds regulant functionality.
  • Silicone polymers have also found widespread application in the textile industry to provide fiber properties inclusive of softness, water proofing and easy ironing. To that effect the silicone polymers are applied (in the textile industry) to the fabrics during manufacture or during make-up of clothing, in the form of relatively concentrated dispersions or solutions either by padding or spray-on. Often, especially for long lasting softness, water proofing treatment or other benefits, mixtures or organofunctional polydialkylsiloxanes are used. The fabrics are subsequently treated with catalysts or heated to cause crosslinking of setting of the silicone polymers.
  • German Patent 27 54 704 discloses a treating agent consisting of a polydimethylsiloxane containing dia- minoalkyl groups for providing softness to natural and synthetic fabrics.
  • Japanese Patent 79,131,096 pertains to a treating agent consisting of a mixture of polydimethylsiloxane with NHR-groups and a polydimethylsiloxane with hydroxy groups, for providing softness to acrylics.
  • the fabrics are spray coated and then heated for curing.
  • German Patent 20 16 095 uses polydimethylsiloxane containing pendant epoxy groups for providing softness and smoothness to synthetic organic fabrics.
  • US Patent 4,247,592 discloses a treating agent consisting of a polydimethylsiloxane containing diami- noalkyl groups in providing softness to fire retardant synthetic textile.
  • the treating agent is applied by brushing, rinsing, padding, dipping and spraying, and is then durably affixed to the textile by heating.
  • European Patent 058 493 relates to a treating agent mixture of an organo polysiloxane containing diami- noalkyl and polyoxyalkylene groups, with an organopolysiloxane containing carboxylic acid ester groups orwith an organopolysiloxane containing epoxy and polyalkylene groups.
  • the mixture is added by spray-on and treated for curing. It is said to provide softness, anti-wrinklig and long lasting electrostatic prevention benefits.
  • German Patent application DOS. 26.31.419 relates to fabric rinse softening compositions containing a fabric-substantive cationic component and a polydimethylsiloxane possibly amino substituted. The mixture is applied as an aqueous dispersion.
  • This invention is based on the discovery that liquid detergent compositions capable of simultaneously providing fibre-cleaning and textile handling benefits, inclusive of softness, can now be formulated containing a binary component systems and an organo-functional siloxane.
  • compositions herein comprise:
  • substituted siloxanes are incorporated in liquid detergent compositions containing inorganic builder salts such as (poly)-phosphates.
  • the siloxanes are incorporated in concentrated liquid compositions which are substantially free of builders.
  • the invention herein broadly relates to liquid detergent compositions comprising a surface-active agent, a liquid carrier, an organo-functional polydi-alkylsiloxane textile treatment agent, and, if desirable, conventional detergent additives.
  • a first essential component for use in the compositions of this invention is represented by a surface-active agent selected from the group of anionic, nonionic, amphoteric (ampholytic) and zwitterionic surface-active agents and mixtures thereof, said surface-active agent comprising an anionic surface-active agent
  • nonionic surface-active agent is meant to include semi-polar nonionic surfactants.
  • non-ionic surfactants examples include E.P.A. 0.028.865 page 4, line 23 to page 5, line 10 and page 8 line 14 to page 9, line 4.
  • Adisclosure of zwitterionic and ampholytic surfactants for use herein can also be found in E.P.A. 0.028.865 page 7, line 21 to page 8, line 13.
  • anionic surfactants for use herein can be represented by known synthetic and natural anionic surface-active agent which are known to be suitable for use in detergents and frequently have found commercial application. Suitable synthetic anionic surfactants are described in E.P.A. 0.028.865 page 5, line 12 to line 31.
  • natural anionic surface-active agents for use in this invention can be represented by saturated and unsaturated fatty acids having from 10 to 20 carbon atoms in the alkyl chain or the alkalimetal, earth-alkali- metal and amine or alkanolamine soaps thereof. Preferred fatty acids/soaps have from 12 to 18 carbon atoms in the alkyl chain.
  • fatty acids/soaps suitable for use herein are natural coconut fatty acid containing a majority of C 12 and C 14 acids and tallow fatty acids containing a mixture of saturated and unsaturated C 16 and C 18 -fatty acids/soaps.
  • the surface-active agent is used generally at levels from 5% to 70%. While th surface-active agent may be varied over the broad range depending upon the intended utility of the composition and the quantitative and qualitative definition of the additional ingredients and possibly optional components, two preferred executions can be formulated depending upon the presence of (poly)-phosphate builders.
  • liquid compositions are envisaged which are substantially unbuilt.
  • the surface active agents are frequently used in an amount from 25% to 55% and are represented by a mixture of anionic and nonionic surface-active agents, more preferably in a weight ratio of anionic to nonionic in the range from 4:1 to 1:4.
  • liquid built detergent compositions are contemplated containing from 5% to 25%, preferably from 5% to 15% surface-active agent.
  • the latter ingredient can preferably be represented by a mixture of anionic and nonionic surface-active agents whereby the anionic species represents at least 20% of the sum of anionic and nonionic surface-active agents, an at least 3%, calculated on the detergent composition.
  • the like detergent compositions frequently comprise from 5% to 30%, preferably from 12% to 25% of a detergent builder which can be represented by conventional detergent builders many of which have already found commercial application.
  • a detergent builder which can be represented by conventional detergent builders many of which have already found commercial application.
  • suitable builders include the alkali, often sodium, metal salts of (poly)phosphates, e.g. tripolyphosphoric acid, nitrilotriacetic acid (NTA), citric acid and crystalline, completely hydrated, synthetically prepared zeolite builders having a particle diameter in the range from 0.1 to 10, preferably from 0.1 to 4 micrometers.
  • Suitable zeolite builders are ZEOLITE A, X and P (registered trade marks). Mixtures of detergent builders can also be used.
  • compositions herein can additionally contain, as an optional ingredient, a cationic surfactant.
  • a cationic surfactant Suitable cationic surfactant species for use herein are described in European Patent application 0.028.865, page 5, line 32 to page 7 line 21, this passage being incorporated herein by referene.
  • the cationic surfactants can provide and/or enhance a broad range of textile treatment benefits inclusive of cleaning, feel, and bactericidal advantages.
  • These optional cationic surface-active agents are used in additive levels, such as in levels not exceeding 10% of the cumulative amount of anionic and nonionic surfactants defined hereinbefore, and more preferred in a range from 1% to 5% of the detergent composition.
  • compositions herein contain as a further essential component a liquid carrier, possibly a mixture of liquid carriers.
  • the liquid carrier component can be represented by water and conventional liquid organic carriers.
  • Non-limiting examples of the like organic carriers include lower aliphatic alcohol having from 2 to about 6 carbon atoms and 1 to 3 hydroxyl groups; ethers of diethylene glycol and lower aliphatic mono-alcohols having from 1 to 4 carbon atoms and mixtures thereof.
  • liquid carriers are: ethanol; n-propanol; isopropanol; butanol; 1,2-propanediol; 1,3-propanediol; n-hexanol; monomethyl-, -ethyl-, -propyl, and mono-butyl ethers and di-ethylene glycol.
  • Other organic solvents having a relatively high boiling point and low vapor pressure can also be used, provided they do not react with any of the other ingredients present.
  • the relative quantities of liquid carriers needed to insure the liquid state of the composition can vary depending upon the qualitative and quantitative ingredient parameters in a given composition. However, the adequate choice of the carrier is based on routine determinations well-known in the art.
  • the essential organo-functional siloxane for use herein can be present in levels from 0.05% to 5%, preferably from 0.1%-3%, and most preferably from 0.15%-1%. Using levels below 0.05% will not anymore produce, to any noticeable extent, the claimed benefits whereas the incorporation of levels exceeding 5% will not produce additional benefits commensurate with (proportional to) the level increase.
  • the siloxane component is preferably represented by amino-functional polydialkylsiloxanes which are frequently used in levels from 01 % to 3%, more preferably from 0.15-1.0%.
  • the degree of substitution of preferred siloxanes can be expressed as the molar (moiety) proportion of non-terminal silicones carrying a substituent other than a C 1-4 alkyl group to total non-terminal silicones.
  • the numerical value or the degree of substitution of preferred siloxanes lies in the range from 0.01 to 0.7; preferably from 0.02 to 0.3. While non-terminal substitution is preferred for enhanced through-the-wash fiber substantivity, it is understood that siloxanes with substituted terminal silicone atoms can also be used.
  • n 3 or 4
  • X and Y are, selected independently, hydrogen, - C1-4-alkyl; -C 5-6 -cycloalkyl and -C 2-4 -NH 2 -
  • Preferred organofunctional polydimethyl siloxanes include aminofunctional siloxanes such as:
  • the organofunctional siloxanes have a viscosity in the range from 250 mm 2 /s to 100.000 mm 2 /s, preferably from 250 mm 2 /s to 2000 mm 2 /s.
  • the viscosity of the siloxane is measured on the pure raw material at 25°C with the aid of a BROOKFIELD@ viscometer (LV Digital).
  • the organofunctional polydimethyl siloxanes in addition to the essential substituents defined hereinbefore, can contain polyalkylene oxide chains attached to unsubstituted silicone atoms (in the meaning of this invention).
  • the polyalkylene, such as propylene or ethylene, oxide chains are attached to the silicone atoms instead of a C 1-4 alkyl group.
  • the alkoxylation enhances the hydrophilic and antistatic (charge-reducing) properties of the component in relation to the textiles.
  • compositions herein can contain a series of optional detergent ingredients with a view to improve the composition taking into consideration the specific utilization.
  • optional components can be presented by virtually all substances, which are known to suitable for use in the like composition, for their known functionality in the art established levels.
  • the non-built or built compositions of the invention can contain, in addition to the detergent builder, other types of sequestrants, having precipitation inhibitor or anti-incrustation properties, in varying levels e.g. in an amount from 0.2% to 5%.
  • Such further sequestrants can be water-soluble copolymeric ingredients e.g.: polyacrylates, polymaleates and copolymeric carboxylates including those obtained from the copolymerization of unsaturated polyacids such a maleic or citraconic acid with suitable polymerizable reaction partners such as methacrylic acid, acrylic acid, mesaconic acid and methyl-vinyl-ether. Mixture of the like watersoluble detergent sequestrant can also be used.
  • detergent enzymes such as proteases, amylases, lipases and mixtures thereof, and stablizing agents for the like enzymes, soil suspending agents such as sodium carboxymethylcellulose and polyvinylpyrrolidone, suds regulants, such as C 16-22 fatty acids and methylated polysiloxanes, especially dimethylpolysiloxane, said silicone being used preferably at levels from 0.01 % to 0.4%.
  • Hydrotropes can also be used and are frequently desirable in built compositions.
  • hydrotropes examples include the water-soluble alkylaryl sulfonates having up to 3 carbon atoms in an alkyl group such as sodium, potassium, ammonium, and ethanol amine salts of xylene-, toluene-, ethylbenzene- and isopropyl benzene sulfonic acids.
  • the subject compositions further can comprise brighteners, perfumes, dyes, bactericidal agents, antioxidants, opacifiers, photoactivators, fillers and the like.
  • liquid detergent compositions were prepared by mixing, in a conventional manner, the following ingredients in the stated proportions; the aminofunctional polysiloxane was admixed directly in liquid composition under agitation.
  • compositions of examples I and B were compared for through-the-wash softness versus identical compositions A and B which did not contain the aminofunctional polydimethylsiloxane.
  • the testing conditions were as follows:
  • compositions in accordance with the invention are as follows:

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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)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
EP85200027A 1984-01-25 1985-01-15 Liquid detergent compositions containing organo-functional polysiloxanes Expired - Lifetime EP0150872B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT85200027T ATE51892T1 (de) 1984-01-25 1985-01-15 Fluessige, organo-funktionelle polysiloxane enthaltende detergenszusammensetzungen.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB848401875A GB8401875D0 (en) 1984-01-25 1984-01-25 Liquid detergent compositions
GB8401875 1984-01-25

Publications (3)

Publication Number Publication Date
EP0150872A1 EP0150872A1 (en) 1985-08-07
EP0150872B1 EP0150872B1 (en) 1990-04-11
EP0150872B2 true EP0150872B2 (en) 1993-05-12

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EP85200027A Expired - Lifetime EP0150872B2 (en) 1984-01-25 1985-01-15 Liquid detergent compositions containing organo-functional polysiloxanes

Country Status (8)

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EP (1) EP0150872B2 (ja)
JP (1) JPH0657839B2 (ja)
AT (1) ATE51892T1 (ja)
CA (1) CA1232412A (ja)
DE (1) DE3577107D1 (ja)
GB (1) GB8401875D0 (ja)
GR (1) GR850050B (ja)
MX (1) MX163030B (ja)

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US11624156B2 (en) 2013-12-09 2023-04-11 The Procter & Gamble Company Fibrous structures including an active agent and having a graphic printed thereon

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EP0150872A1 (en) 1985-08-07
ATE51892T1 (de) 1990-04-15
JPS60215099A (ja) 1985-10-28
JPH0657839B2 (ja) 1994-08-03
DE3577107D1 (de) 1990-05-17
EP0150872B1 (en) 1990-04-11
CA1232412A (en) 1988-02-09
GR850050B (ja) 1985-04-18
GB8401875D0 (en) 1984-02-29

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