WO1998000216A1 - Aqueous silicone defoaming agent - Google Patents

Aqueous silicone defoaming agent Download PDF

Info

Publication number
WO1998000216A1
WO1998000216A1 PCT/IB1997/000798 IB9700798W WO9800216A1 WO 1998000216 A1 WO1998000216 A1 WO 1998000216A1 IB 9700798 W IB9700798 W IB 9700798W WO 9800216 A1 WO9800216 A1 WO 9800216A1
Authority
WO
WIPO (PCT)
Prior art keywords
silicone
emulsion
surface active
weight
active agents
Prior art date
Application number
PCT/IB1997/000798
Other languages
French (fr)
Inventor
Terence E. Say
Charles T. Gammon
John J. Gunning, Jr.
Jacques A. Cavezzan
George C. Street
Original Assignee
Rhone-Poulenc Inc.
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 Rhone-Poulenc Inc. filed Critical Rhone-Poulenc Inc.
Priority to AU32700/97A priority Critical patent/AU3270097A/en
Publication of WO1998000216A1 publication Critical patent/WO1998000216A1/en

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
    • 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
    • C11D3/3738Alkoxylated silicones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/894Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D19/00Degasification of liquids
    • B01D19/02Foam dispersion or prevention
    • B01D19/04Foam dispersion or prevention by addition of chemical substances
    • B01D19/0404Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D19/00Degasification of liquids
    • B01D19/02Foam dispersion or prevention
    • B01D19/04Foam dispersion or prevention by addition of chemical substances
    • B01D19/0404Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
    • B01D19/0409Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance compounds containing Si-atoms
    • 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
    • C11D1/82Compounds containing silicon
    • 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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0026Low foaming or foam regulating compositions
    • 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
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C3/00Pulping cellulose-containing materials
    • D21C3/22Other features of pulping processes
    • D21C3/28Prevention of foam
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/06Paper forming aids
    • D21H21/12Defoamers

Definitions

  • the present invention relates to novel defoaming agent which can be used for a variety of applications More specifically, the invention comprises a completely aqueous silicone defoaming agent which includes a silicone fluid, silica, non-silicone containing surface active agents silicone containing surface active agents and water
  • a completely aqueous silicone defoaming agent which includes a silicone fluid, silica, non-silicone containing surface active agents silicone containing surface active agents and water
  • the composition has particular use in aqueous pulp defoaming applications
  • composition demonstrating utility as a defoaming agent
  • the composition comprises an aqueous emulsion of the following components
  • composition does not contain any hydrocarbons
  • the amount of solids in the emulsion ranges from about 10 to about 60 percent by weight
  • the emulsion may also include performance enhancing additives such as thickeners, biocides, acids bases and the like
  • the Figure is a graphical representation of the knockdown properties of the inventive material as compared to several commercially available defoamers
  • the present invention relates to a multi-component blend composition in aqueous emulsion form which demonstrates excellent defoaming or antifoammg properties
  • the first component of the blend composition is one or more silicone fluids
  • silicone fluids are well known in the art and comprise polyorganosiloxanes having a viscosity ranging from between about 50 to about 30000 centistokes at 25°C
  • These fluids are usually of the formula R 1(a) S ⁇ O (4 - a)/2 , wherein R, which may be the same or different, are monovalent or halogenated hydrocarbon groups having one to ten carbon atoms Specific examples of such groups include methyl , ethyl, propyl butyl, octyl t ⁇ fluoropropyl, phenyl 2-phenylethyl and vinyl groups, and wherein a has a value between about 0 and about 4, more preferably between about 1 9 to about 2 2 It is particularly preferred that the fluid comprises a trimethylsilyl-terminated polydimethylsiloxane Alternatively, the fluid may be of the formula R 2 (b)( 30),SiO ( -, i
  • silicone fluids can be used to yield a composition having a desirable viscosity More preferred is the use of a fluid or mixtures of fluids having a viscosity ranging from between about 200 to about 2000 centistokes at 25°C, and even more preferred is the use of a fluid or mixtures of fluids having a viscosity of about 1000 centistokes at 25°C
  • silicone fluids useful in association with the present invention are disclosed in U S Patent No 5,380 464 To the extent necessary for completion this patent is hereby incorporated by reference
  • a commercial silicone fluid which may be selected for use in the present invention comprises Rhodorsil® 47-V 1000 centistoke silicone fluid manufactured by Rh ⁇ ne-Poulenc
  • the amount of the silicone fluid in the emulsion typically ranges from about 5 to about 50 percent by weight of the emulsion with amounts of about 10 to about 30 percent by weight being more preferred and amounts ranging from about 15 to about 25 percent by weight being most preferred
  • the second component of the inventive composition comprises one or more silicone containing surface active agents
  • silicone containing surface active agents This encompasses any and all silicone containing materials which both includes one or more hydrophobic groups and demonstrates surface active properties
  • Particularly preferred are the use of silicone polymers which include alkoxylate groups such as ethylene oxide, propylene oxide, and mixtures thereof
  • Examples of silicone surface active agents which may be selected for use in the present composition are disclosed in the following patent documents U S 5,104,647, U S 5,017,216, U S 5 145,978, US 5,145,977 and WO 94/22311 To the extent necessary for completion these patents are hereby expressly incorporated by reference Generally these materials are silicone glycols or polyether modified siloxanes Classes of such materials include the polymerization product of one or more polyalkyl or aryl silicone or siloxane monomers with one or more polyoxyalkyl monomers Specifically useful surface active agents include dimethyl, 3-hydroxypropyl ethoxylated-propoxylated siloxa
  • the amount of the silicone containing surface active agent in the emulsion typically ranges from about 2 to about 20 percent by weight of the emulsion with amounts of about 5 to about 15 percent by weight being more preferred and amounts ranging from about 6 to about 12 percent by weight being most preferred It is believed that the high level of silicone containing surface active agent enables the resulting emulsion to have high temperature stability and superior foam knockdown properties
  • the third component of the composition is one or more non-silicone containing surface active agents
  • surface active agents are any materials which are capable of functioning to emulsify the silicone fluid in an aqueous environment and which do not contain silicone atoms
  • the surface active agents may take the form of either surfactants or protective colloids When selecting a surfactant for use, either anionic cationic, amphotenc, noniomic surfactants or mixtures thereof may be selected
  • surfactants which may be selected include polyethylene glycol mono- and diesters of mono- or polyunsaturated acids, saturated fatty acids, polyoxyethylene sorbitan monooleate, ammonium lauryl ether sulfate, sodium lauryl ether sulfate octyl phenol ethoxylates (30-50 moles of ethylene oxide), nonyl phenol ethoxylates (30-50 moles of ethylene oxide) sodium lauryl sulfate, and phosphate esters such as ammonium or sodium salts of poly(oxy-1 ,2- ethaned ⁇ yl), ⁇ -(nonylphenol)- ⁇ -hydroxy-phosphate, poly(oxy-1 2-ethaned ⁇ yl) ⁇ -phenol- ⁇ )-hydroxy- phosphate and poly(oxy-1 ,2-ethaned ⁇ yl), ⁇ -(octylphenol)- ⁇ -hydroxy-phosphate
  • protective colloids which may be selected include polyfvmyl alcohol] e
  • mixtures of surfactants may be selected.
  • a particularly efficacious mixture is the combination of sorbitan monostearate (e g , Span 60) with ethoxylated stea ⁇ c acid (having 40 moles of ethylene oxide per molecule)
  • sorbitan monostearate e g , Span 60
  • ethoxylated stea ⁇ c acid having 40 moles of ethylene oxide per molecule
  • Myrj 52 sold by ICI Americas
  • the amount of this third component in the emulsion typically ranges from about 1 to about 10 percent by weight of the emulsion with amounts of about 2 to about 8 percent by weight being more preferred and amounts ranging from about 3 to about 7 percent by weight being most preferred
  • the fourth component in the emulsion comprises a solid particulate material which is rendered hydrophobic when in a silicone fluid
  • the most preferred solid particulate comprises silica including precipitated, pyrogenic, fumed silica and mixtures thereof
  • the silica selected should ideally have a surface area of greater than about 100 m 2 /gram
  • the particle size of the silica typically ranges from about 0 1 to about 20 microns, with a particle size of between about 1 micron and about 15 microns being more preferred
  • the following solid particulate materials may alternatively be selected clay, talc, titanium dioxide, aluminum oxide, zirconium oxide and mixtures of the above Mixtures of the materials of this paragraph with silica are expressly covered by this invention
  • the amount of this fourth component in the emulsion typically ranges from about 0 5 to about 5 percent by weight of the emulsion
  • performance enhancing and stabilizing chemicals which can function to provide specific properties to the final emulsion
  • examples of such chemicals include bio ⁇ des, acids, bases, dyes, corrosion inhibitors, thickening agents (e g , polygalactomannans, polyacrylates and the like), enzymes and the like
  • bio ⁇ des e.g , biogalactomannans, polyacrylates and the like
  • thickening agents e g , polygalactomannans, polyacrylates and the like
  • enzymes and the like In practice the amount of these additives is no more than 10 percent by weight of the emulsion
  • a particularly preferred optional additive is a non-hydrocarbon silicone performance additive
  • PULPSIL® silicone chemicals which are manufactured by Wacker-Chimie
  • the most preferred of such chemicals is PULPSIL® 160C, which, according to the manufacturer is a silicone compound which is a colorless cloudy liquid having a specific gravity at 25°C of 0 99-1 01 g/cm 3 , a Refractive index at 25°C of 1 4020-1 4100, a variable viscosity at 25°C a maximum volatility of 2% at 5g, 2 hours 180°C and a shelf life of 12 months
  • Another useful specialty additive comprises the PULPAID silicone chemicals which are manufactured by Dow Corning Particularly useful is PULPAID 3472 Concentrate which according to the manufacturer is a 100 percent concentrate which is a cream white emulsion which has as active ingredients silica-filled polydimethylsiloxane and silicone organic copolymers This compound has a specific gravity of 1 0,
  • the final component of the emulsion is the aqueous emulsifying medium, typically water
  • the emulsion does not contain any hydrocarbons (e g , organic solvents such as kerosene, mineral oils, etc )
  • the emulsion of the present invention contains between about 10 and about 60 percent solids by weight, with amounts between about 15 and about 50 percent solids by weight being more preferred and amounts between about 20 and about 40 percent solids by weight being most preferred
  • the viscosity of the emulsion typically ranges between about 100 and about 30000 cps as measured by a Brookfteld Viscometer, Spindle #3, 60 rpm, with a viscosity of between about 200 and about 2000 cps being more preferred
  • Preparation of the inventive emulsion simply comprises a simple sequential mixture of the various components under preferred heating and agitation conditions In practice the solid particulate material is first mixed into the silicone fluid under heat and pressure (2000 psi for homogenization) and agitation sufficient to yield a homogenous material This homogenous material is thereafter added to a vessel containing water and the non-silicone containing surface active agent followed by addition of the silicone containing surface active agent Thereafter optional bases thickening agents, and the like are added and the
  • the above synthesized emulsion may be used in any application where foam reduction is desired such as in personal care products, agricultural applications detergents and cleaners and in paper mill operations
  • a particularly preferred use of the novel composition is in Kraft pulp liquor defoaming
  • the above defined emulsion is simply added to an acidic, basic or neutral aqueous foaming (or foam- producing) system
  • the foam control emulsions of the present invention are added at a concentration of about 10 ppm to about 0 1 percent based on the weight of the foaming system
  • the emulsions of the present invention provide the following advantages as compared to prior art systems which require the presence of hydrocarbons environmentally safe and friendly, easy to process, and, when used in paper mills the emulsion does not contribute to deposit formation
  • mineral oils and other hydrocarbons typically present in defoaming agents tackify naturally occumng wood pitch making the colloidal particles more susceptible to agglomeration thereby increasing the probability of the formation of deposits
  • hydrocarbon present in the inventive emulsion there is a much reduced risk of deposit formation
  • they have an extremely long shelf life, with the emulsion demonstrating stability for greater than 30 days, more preferably greater than 90 days and most preferably greater than 180 days being possible This stability is demonstrated even at high storage temperatures (i e greater than about 40°C)
  • silicone base Approximately 91 parts of a 1000 centistoke silicone fluid is added to a vessel and the vessel is heated to 120°F Approximately 9 parts of silica is added to the vessel and it is mixed until the lumps in the vessel disappear The contents are then homogenized at 2000 psi to yield what is defined as the silicone base
  • ethoxylated stea ⁇ c acid having 40 moles of ethylene oxide per mole of molecule
  • 3 0 parts of sorbitan monostearate are added to 62 75 parts of water and the mixture is heated to 150°F and mixed and held at this temperature for 30 minutes 23 025 parts of the silicone base are then pumped into this mixture followed by the addition of 6 975 parts of a silicone surfactant which is a dimethyl, 3-hydroxypropyl ethoxylated-propoxylated siloxane and/or silicone (CAS Registration No 68937-55-3) and the contents are mixed for 30 minutes 2 5 parts of a polyacrylate dispersant diluted with 50 percent water is added and the mixture is mixed for 30 minutes 0 150 parts of NaOH (50% solution) are then added the mixture is agitated for 30 minutes and the vessel contents are allowed to cool to about 90-100°F 0 100 parts of a biocide which is a 20% solution of 1 ,2-benz ⁇ soth ⁇ a
  • the resulting product is a creamy white liquid having a specific gravity of between about 0 98 and 1 02
  • the viscosity of the material at 25°C is between about 800 and 1300 cps as measured by a Brookfield Viscometer, Spindle #3, 60 rp , the pH is between 7 5 and 9 0 and the percent solids is 35 percent
  • Sample B Commercial product made by Nottingham Chemical (400 ⁇ l aliquot)
  • Sample C Commercial product made by Basso (530 ⁇ l aliquot)
  • Sample D Commercial product made by Callaway Chemical (400 ⁇ l aliquot)
  • Sample E Commercial product made by Henkel Chemical (400 ⁇ l aliquot)
  • inventive composition of the present invention provides excellent defoaming properties These properties include excellent knockdown and maintenance of a low foam height for extended periods of time.
  • inventive compositions of the present invention provides excellent defoaming properties
  • Example 1 To 100 parts of the composition of Example 1 are added about 3 5 parts of either PULPAID 3472, manufactured by Dow Corning, or PULPSIL® 160-C manufactured by Wacker-Chimie The resulting compositions are tested using the above Test Data procedures While the initial knockdown values for these two compositions are comparable to those of the Example 1 composition, the foam height remains at a low value for extended periods of time This phenomenon is particularly seen at times of between 60 seconds and 120 seconds after addition of the emulsion composition This Example demonstrates that an even better performance can be obtained by the addition of small amounts of specialty additives to the emulsion

Abstract

A composition comprising an aqueous emulsion of the following components: a) one or more silicone fluids; b) one or more silicone containing surface active agents; c) one or more non-silicone containing surface active agents; and d) a solid particulate material which is rendered hydrophobic in said one or more silicone fluids; wherein said composition does not contain any hydrocarbons is provided.

Description

AQUEOUS SILICONE DEFOAMING AGENT
Background of the Invention
1 Field of the Invention
The present invention relates to novel defoaming agent which can be used for a variety of applications More specifically, the invention comprises a completely aqueous silicone defoaming agent which includes a silicone fluid, silica, non-silicone containing surface active agents silicone containing surface active agents and water The composition has particular use in aqueous pulp defoaming applications
2 Technology Description
The use of silicone containing compositions in paper mill pulp defoaming operations has met with a great deal of commercial success Examples of such materials are described in the following patent publications CA 2048823, US 4,076,648, CA 880850 and US 5,380,464 While these types of materials have significantly advanced the art, they typically require the presence of an organic solvent such as a hydrocarbon (including, for example, mineral oils) Such products may not be ultimately desirable for use in commercial operations because of the presence of the volatile organic solvent which can create environmental concerns and cause the formation of pitch and other deposits on resulting paper because of the presence of solvent This latter concern is independent of the amount of volatiles in the hydrocarbon
Despite the above teachings, there still exists a need in the art for a silicone containing composition having no hydrocarbons which has functionality as a defoaming agent and which demonstrates excellent stability properties Brief Summary of the Invention
In accordance with the present invention a novel composition demonstrating utility as a defoaming agent is provided The composition comprises an aqueous emulsion of the following components
a) one or more silicone fluids,
b) one or more silicone containing surface active agents
c) one or more non-silicone containing surface active agents and
d) a solid particulate material which is rendered hydrophobic in said one or more silicone fluids
wherein said composition does not contain any hydrocarbons
In particularly preferred embodiments, the amount of solids in the emulsion ranges from about 10 to about 60 percent by weight In addition to the above materials, the emulsion may also include performance enhancing additives such as thickeners, biocides, acids bases and the like
Another embodiment of the present invention comprises a process for reducing the foam tn a foam containing liquid by adding to said foam containing liquid an effective defoaming amount of the above defined novel defoaming composition
A preferred embodiment of this aspect of the present invention is where the foam containing liquid to be treated is Kraft pulp liquor
An object of the present invention is to provide a novel composition which contains no organic solvents and is capable of functioning as a defoaming agent Still another object of the present invention is to provide a process for reducing the foam of a foam containing liquid by utilizing the novel composition of the present invention
These, and other objects, will readily be apparent to those skilled in the art as reference is made to the drawing and detailed description of the preferred embodiment
Brief Description of the Drawing
The Figure is a graphical representation of the knockdown properties of the inventive material as compared to several commercially available defoamers
Detailed Description of the Preferred Embodiment
In describing the preferred embodiment, certain terminology will be utilized for the sake of clarity Such terminology is intended to encompass the recited embodiment, as well as all technical equivalents which operate in a similar manner for a similar purpose to achieve a similar result
The present invention relates to a multi-component blend composition in aqueous emulsion form which demonstrates excellent defoaming or antifoammg properties
The first component of the blend composition is one or more silicone fluids Such fluids are well known in the art and comprise polyorganosiloxanes having a viscosity ranging from between about 50 to about 30000 centistokes at 25°C These fluids are usually of the formula R1(a)SιO(4-a)/2, wherein R,, which may be the same or different, are monovalent or halogenated hydrocarbon groups having one to ten carbon atoms Specific examples of such groups include methyl, ethyl, propyl butyl, octyl tπfluoropropyl, phenyl 2-phenylethyl and vinyl groups, and wherein a has a value between about 0 and about 4, more preferably between about 1 9 to about 2 2 It is particularly preferred that the fluid comprises a trimethylsilyl-terminated polydimethylsiloxane Alternatively, the fluid may be of the formula R2(b)( 30),SiO(-, i,o: wherein R2 is the same as defined above for Ri, R3 is a hydrogen atom or R2, and the -OR3 group is present at least at the end of a molecular chain of polyorganosiloxane The value of b is between about 0 to about 4 more preferably between about 1 9 and 2 2, and c has a value so as to provide at least one -OR3 group per molecule Such an alternative fluid is preferably a hydroxyl-terminated polydimethylsiloxane
Mixtures of silicone fluids can be used to yield a composition having a desirable viscosity More preferred is the use of a fluid or mixtures of fluids having a viscosity ranging from between about 200 to about 2000 centistokes at 25°C, and even more preferred is the use of a fluid or mixtures of fluids having a viscosity of about 1000 centistokes at 25°C
Examples of silicone fluids useful in association with the present invention are disclosed in U S Patent No 5,380 464 To the extent necessary for completion this patent is hereby incorporated by reference A commercial silicone fluid which may be selected for use in the present invention comprises Rhodorsil® 47-V 1000 centistoke silicone fluid manufactured by Rhόne-Poulenc
The amount of the silicone fluid in the emulsion typically ranges from about 5 to about 50 percent by weight of the emulsion with amounts of about 10 to about 30 percent by weight being more preferred and amounts ranging from about 15 to about 25 percent by weight being most preferred
The second component of the inventive composition comprises one or more silicone containing surface active agents This encompasses any and all silicone containing materials which both includes one or more hydrophobic groups and demonstrates surface active properties Particularly preferred are the use of silicone polymers which include alkoxylate groups such as ethylene oxide, propylene oxide, and mixtures thereof Examples of silicone surface active agents which may be selected for use in the present composition are disclosed in the following patent documents U S 5,104,647, U S 5,017,216, U S 5 145,978, US 5,145,977 and WO 94/22311 To the extent necessary for completion these patents are hereby expressly incorporated by reference Generally these materials are silicone glycols or polyether modified siloxanes Classes of such materials include the polymerization product of one or more polyalkyl or aryl silicone or siloxane monomers with one or more polyoxyalkyl monomers Specifically useful surface active agents include dimethyl, 3-hydroxypropyl ethoxylated-propoxylated siloxanes and silicones (CAS Registration No 68937-55-3) (the presence of the 3-hydroxypropyl group is considered optional) and the copolymer of polyalkyieneoxide methyl siloxane and polyalkylene oxide monomers (CAS Registration No 71965-38-3) Commercial materials which may be selected as the silicone surface active agent include the Silquest® DA products manufactured by OSi Specialties Inc and the Tegopren line of materials manufactured by Goldschmidt
The amount of the silicone containing surface active agent in the emulsion typically ranges from about 2 to about 20 percent by weight of the emulsion with amounts of about 5 to about 15 percent by weight being more preferred and amounts ranging from about 6 to about 12 percent by weight being most preferred It is believed that the high level of silicone containing surface active agent enables the resulting emulsion to have high temperature stability and superior foam knockdown properties
The third component of the composition is one or more non-silicone containing surface active agents These are any materials which are capable of functioning to emulsify the silicone fluid in an aqueous environment and which do not contain silicone atoms The surface active agents may take the form of either surfactants or protective colloids When selecting a surfactant for use, either anionic cationic, amphotenc, noniomic surfactants or mixtures thereof may be selected
Specific examples of surfactants which may be selected include polyethylene glycol mono- and diesters of mono- or polyunsaturated acids, saturated fatty acids, polyoxyethylene sorbitan monooleate, ammonium lauryl ether sulfate, sodium lauryl ether sulfate octyl phenol ethoxylates (30-50 moles of ethylene oxide), nonyl phenol ethoxylates (30-50 moles of ethylene oxide) sodium lauryl sulfate, and phosphate esters such as ammonium or sodium salts of poly(oxy-1 ,2- ethanedιyl),σ-(nonylphenol)-ω-hydroxy-phosphate, poly(oxy-1 2-ethanedιyl) σ-phenol-< )-hydroxy- phosphate and poly(oxy-1 ,2-ethanedιyl),σ-(octylphenol)-ω-hydroxy-phosphate Examples of protective colloids which may be selected include polyfvmyl alcohol] ethyl cellulose, poly[vιnyl pyrollidone], sodium polyacrylate and natural gums such as xanthan gum
In the preferred embodiment, mixtures of surfactants may be selected A particularly efficacious mixture is the combination of sorbitan monostearate (e g , Span 60) with ethoxylated steaπc acid (having 40 moles of ethylene oxide per molecule) A commercial example of this type of surfactant is Myrj 52, sold by ICI Americas
The amount of this third component in the emulsion typically ranges from about 1 to about 10 percent by weight of the emulsion with amounts of about 2 to about 8 percent by weight being more preferred and amounts ranging from about 3 to about 7 percent by weight being most preferred
The fourth component in the emulsion comprises a solid particulate material which is rendered hydrophobic when in a silicone fluid The most preferred solid particulate comprises silica including precipitated, pyrogenic, fumed silica and mixtures thereof The silica selected should ideally have a surface area of greater than about 100 m2/gram The particle size of the silica typically ranges from about 0 1 to about 20 microns, with a particle size of between about 1 micron and about 15 microns being more preferred
As a substitute for silica, the following solid particulate materials may alternatively be selected clay, talc, titanium dioxide, aluminum oxide, zirconium oxide and mixtures of the above Mixtures of the materials of this paragraph with silica are expressly covered by this invention
The amount of this fourth component in the emulsion typically ranges from about 0 5 to about 5 percent by weight of the emulsion
Also optionally present in the emulsion are performance enhancing and stabilizing chemicals which can function to provide specific properties to the final emulsion Examples of such chemicals include bioαdes, acids, bases, dyes, corrosion inhibitors, thickening agents (e g , polygalactomannans, polyacrylates and the like), enzymes and the like In practice the amount of these additives is no more than 10 percent by weight of the emulsion
A particularly preferred optional additive is a non-hydrocarbon silicone performance additive These materials provide improved durability or longevity of the defoaming activity Examples of such additives include the PULPSIL® silicone chemicals which are manufactured by Wacker-Chimie The most preferred of such chemicals is PULPSIL® 160C, which, according to the manufacturer is a silicone compound which is a colorless cloudy liquid having a specific gravity at 25°C of 0 99-1 01 g/cm3, a Refractive index at 25°C of 1 4020-1 4100, a variable viscosity at 25°C a maximum volatility of 2% at 5g, 2 hours 180°C and a shelf life of 12 months Another useful specialty additive comprises the PULPAID silicone chemicals which are manufactured by Dow Corning Particularly useful is PULPAID 3472 Concentrate which according to the manufacturer is a 100 percent concentrate which is a cream white emulsion which has as active ingredients silica-filled polydimethylsiloxane and silicone organic copolymers This compound has a specific gravity of 1 0, a viscosity of 20,000 - 30,000 cps at 25°C and a flash point greater than 100°C These specialty additive compounds allegedly comply with FDA §§ 176 170, 176 180 and 176 210 and BGA XXXVI In practice, the specialty additives should be present in amounts ranging from about 0 25 to about 10 0 percent by weight of the final emulsion
The final component of the emulsion is the aqueous emulsifying medium, typically water
The emulsion does not contain any hydrocarbons (e g , organic solvents such as kerosene, mineral oils, etc )
The emulsion of the present invention contains between about 10 and about 60 percent solids by weight, with amounts between about 15 and about 50 percent solids by weight being more preferred and amounts between about 20 and about 40 percent solids by weight being most preferred The viscosity of the emulsion typically ranges between about 100 and about 30000 cps as measured by a Brookfteld Viscometer, Spindle #3, 60 rpm, with a viscosity of between about 200 and about 2000 cps being more preferred Preparation of the inventive emulsion simply comprises a simple sequential mixture of the various components under preferred heating and agitation conditions In practice the solid particulate material is first mixed into the silicone fluid under heat and pressure (2000 psi for homogenization) and agitation sufficient to yield a homogenous material This homogenous material is thereafter added to a vessel containing water and the non-silicone containing surface active agent followed by addition of the silicone containing surface active agent Thereafter optional bases thickening agents, and the like are added and the emulsion is mixed until it is completely homogenous
The above synthesized emulsion may be used in any application where foam reduction is desired such as in personal care products, agricultural applications detergents and cleaners and in paper mill operations A particularly preferred use of the novel composition is in Kraft pulp liquor defoaming
To utilize the emulsion of the present invention to control foam in aqueous foaming systems the above defined emulsion is simply added to an acidic, basic or neutral aqueous foaming (or foam- producing) system Typically, the foam control emulsions of the present invention are added at a concentration of about 10 ppm to about 0 1 percent based on the weight of the foaming system However, the skilled artisan will readily determine optimum concentrations after a few routine experiments
The emulsions of the present invention provide the following advantages as compared to prior art systems which require the presence of hydrocarbons environmentally safe and friendly, easy to process, and, when used in paper mills the emulsion does not contribute to deposit formation It is well known that mineral oils and other hydrocarbons typically present in defoaming agents tackify naturally occumng wood pitch making the colloidal particles more susceptible to agglomeration thereby increasing the probability of the formation of deposits Since there is no hydrocarbon present in the inventive emulsion there is a much reduced risk of deposit formation In addition, they have an extremely long shelf life, with the emulsion demonstrating stability for greater than 30 days, more preferably greater than 90 days and most preferably greater than 180 days being possible This stability is demonstrated even at high storage temperatures (i e greater than about 40°C)
The invention is described in greater detail by the following non-limiting examples
Example 1
Approximately 91 parts of a 1000 centistoke silicone fluid is added to a vessel and the vessel is heated to 120°F Approximately 9 parts of silica is added to the vessel and it is mixed until the lumps in the vessel disappear The contents are then homogenized at 2000 psi to yield what is defined as the silicone base
In a separate vessel 1 5 parts of ethoxylated steaπc acid (having 40 moles of ethylene oxide per mole of molecule) and 3 0 parts of sorbitan monostearate are added to 62 75 parts of water and the mixture is heated to 150°F and mixed and held at this temperature for 30 minutes 23 025 parts of the silicone base are then pumped into this mixture followed by the addition of 6 975 parts of a silicone surfactant which is a dimethyl, 3-hydroxypropyl ethoxylated-propoxylated siloxane and/or silicone (CAS Registration No 68937-55-3) and the contents are mixed for 30 minutes 2 5 parts of a polyacrylate dispersant diluted with 50 percent water is added and the mixture is mixed for 30 minutes 0 150 parts of NaOH (50% solution) are then added the mixture is agitated for 30 minutes and the vessel contents are allowed to cool to about 90-100°F 0 100 parts of a biocide which is a 20% solution of 1 ,2-benzιsothιazolιn-3-one in dipropylene glycol are then added and the entire vessel contents are mixed until homogenous If it is necessary to modify the pH and viscosity of the final product a polyacrylate dispersant (Colloid 1560, Rhόne-Poulenc Inc ) and NaOH may be added to the mixture
The resulting product is a creamy white liquid having a specific gravity of between about 0 98 and 1 02 The viscosity of the material at 25°C is between about 800 and 1300 cps as measured by a Brookfield Viscometer, Spindle #3, 60 rp , the pH is between 7 5 and 9 0 and the percent solids is 35 percent
Test Data
To determine the usefulness of the above composition as a pulp defoamer the following procedure is performed 400 mis of black liquor from a paper mill located in the Southeast part of the United States is heated to 85°C The liquor is transferred into a laboratory "Foam-Cel" foam tester and the rheostat on the tester is activated to 80% to 100% of line voltage (120 volts), thereby starting the pump of the tester This causes the foam in the black liquor to rise When the foam level reaches 24 cm, a specific aliquot of defoaming chemical is added to the tester The level of foam is measured on a periodic basis (every 15 seconds) until the foam level reaches its upper limit (28 cm) and the rheostat is turned off The first reading, which occurs at the time of aliquot addition, is referred to the "Knockdown" time
The following emulsion materials are tested to determine their effectiveness
Sample A - Example 1 Composition (400 μl aliquot)
Sample B - Commercial product made by Nottingham Chemical (400 μl aliquot) Sample C - Commercial product made by Basso (530 μl aliquot)
Sample D - Commercial product made by Callaway Chemical (400 μl aliquot) Sample E - Commercial product made by Henkel Chemical (400 μl aliquot)
The tests are conducted in triplicate Results are shown in the attached table All height measurements are in centimeters and all time measurements are in seconds
Figure imgf000013_0001
The Figure depicts this data in graphical form except the results for Sample B, which are omitted
The above data demonstrates that the inventive composition of the present invention provides excellent defoaming properties These properties include excellent knockdown and maintenance of a low foam height for extended periods of time In addition, because they are completely solvent- free, they are more environmentally desirable compositions and will not contribute to the formation of organic deposition because they do not contain volatile organic solvents or hydrocarbons
Example 2
To 100 parts of the composition of Example 1 are added about 3 5 parts of either PULPAID 3472, manufactured by Dow Corning, or PULPSIL® 160-C manufactured by Wacker-Chimie The resulting compositions are tested using the above Test Data procedures While the initial knockdown values for these two compositions are comparable to those of the Example 1 composition, the foam height remains at a low value for extended periods of time This phenomenon is particularly seen at times of between 60 seconds and 120 seconds after addition of the emulsion composition This Example demonstrates that an even better performance can be obtained by the addition of small amounts of specialty additives to the emulsion
Having described the invention in detail and by reference to the preferred embodiments thereof, it will be apparent that modifications and variations are possible without departing from the scope of the appended claims

Claims

WHAT IS CL-AIMED IS
1 A composition comprising an aqueous emulsion of the following components
a) one or more silicone fluids,
b) one or more silicone containing surface active agents,
c) one or more non-silicone containing surface active agents, and
d) a solid particulate material which is rendered hydrophobic in said one or more silicone fluids,
wherein said composition does not contain any hydrocarbons
2 The composition according to claim 1 wherein
said one or more silicone fluids comprises a polyorganosiloxane having a viscosity of between about 50 to about 30000 centistokes at 25°C
said one or more silicone containing surface active agents is selected from the group consisting of alkoxylated silicone polymers, silicone glycols and polyether modified siloxanes and mixtures thereof,
said one or more non-silicone containing surface active agents is selected from the group consisting of anionic surfactants, cationic surfactants, nonionic surfactants, amphoteπc surfactants, protective colloids and mixtures thereof, and
said solid particulate material is selected from the group consisting of precipitated silica, pyrogenic silica, fumed silica, clay, talc, titanium dioxide, aluminum oxide zirconium oxide and mixtures thereof
3 The composition according to claim 2 wherein the amounts of components (a), (b) , (c) and (d) by weight of the emulsion are as follows
(a) about 5 to about 50 percent by weight
(b) about 2 to about 20 percent by weight,
(c) about 1 to about 10 percent by weight and
(d) about 0 5 to about 5 percent by weight
wherein the sum of the weight percentages of (a) (b), (c) and (d) is between about 10 and about 60
4 The composition according to claim 1 further comprising one or more of the following materials biocides, acids, bases, dyes, corrosion inhibitors thickening agents, enzymes and non-hydrocarbon silicone performance additives
5 The composition according to claim 4 comprising a non-hydrocarbon silicone performance additive present in an amount of about 0 25 to about 10 0 percent by weight of the emulsion
6 An emulsion consisting essentially of
a) a silicone fluid which is a polyorganosiloxane having a viscosity of between about 50 to about 30000 centistokes at 25°C, present in an amount of about 5 to about 50 percent by weight of the emulsion,
b) a silicone containing surface active agent which is a dimethyl, 3-hydroxypropyl ethoxylated- propoxylated siloxane or silicone present in an amount of about 2 to about 20 percent by weight of the emulsion
c) one or more non-silicone containing surface active agents which comprises sorbitan monostearate and ethoxylated steaπc acid, the combination of which is present in an amount of about 1 to about 10 percent by weight of the emulsion
d) a solid particulate silica material which is rendered hydrophobic in said one or more silicone fluids present in an amount of about 0 5 to about 5 percent by weight of the emulsion and
e) the balance, water
7 The composition according to claim 6 further comprising one or more of the following materials biocides, acids, bases dyes corrosion inhibitors thickening agents enzymes and non-hydrocarbon silicone performance additives
8 A process for reducing the level of foam in a foam containing liquid comprising the step of adding to said foam containing liquid an effective foam reducing amount of an aqueous emulsion of the following components
a) one or more silicone fluids,
b) one or more silicone containing surface active agents,
c) one or more non-silicone containing surface active agents, and
d) a solid particulate material which is rendered hydrophobic in said one or more silicone fluids,
wherein said composition does not contain any hydrocarbons 9 The process according to claim 8 wherein
said one or more silicone fluids comprises a polyorganosiloxane having a viscosity of between about 50 to about 30000 centistokes at 25°C,
said one or more silicone containing surface active agents is selected from the group consisting of alkoxylated silicone polymers, silicone glycols and polyether modified siloxanes and mixtures thereof,
said one or more non-silicone containing surface active agents is selected from the group consisting of anionic surfactants cationic surfactants nonionic surfactants amphotenc surfactants protective colloids and mixtures thereof and
said solid particulate material is selected from the group consisting of precipitated silica, pyrogenic silica, fumed silica, clay, talc, titanium dioxide, aluminum oxide, zirconium oxide and mixtures thereof
10 The process according to claim 9 wherein said foam containing liquid comprises pulp liquor from a paper mill
11 A personal care product agricultural chemical detergent composition cleaning composition or paper mill chemical including an aqueous emulsion of the following components
a) one or more silicone fluids,
b) one or more silicone containing surface active agents,
c) one or more non-silicone containing surface active agents and d) a solid particulate material which is rendered hydrophobic in said one or more silicone fluids,
wherein said emulsion does not contain any hydrocarbons
PCT/IB1997/000798 1996-07-02 1997-06-27 Aqueous silicone defoaming agent WO1998000216A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU32700/97A AU3270097A (en) 1996-07-02 1997-06-27 Aqueous silicone defoaming agent

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US2114196P 1996-07-02 1996-07-02
US60/021,141 1996-07-02
US87705397A 1997-06-17 1997-06-17
US08/877,053 1997-06-17

Publications (1)

Publication Number Publication Date
WO1998000216A1 true WO1998000216A1 (en) 1998-01-08

Family

ID=26694317

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB1997/000798 WO1998000216A1 (en) 1996-07-02 1997-06-27 Aqueous silicone defoaming agent

Country Status (2)

Country Link
AU (1) AU3270097A (en)
WO (1) WO1998000216A1 (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000036063A1 (en) * 1998-12-11 2000-06-22 Henkel Kommanditgesellschaft Auf Aktien Aqueous foam control emulsion
US6521586B1 (en) 1999-08-13 2003-02-18 Dow Corning S.A. Silicone foam control agent
US6521587B1 (en) 1999-08-13 2003-02-18 Dow Corning S.A. Silicone foam control agent
US6605183B1 (en) 1999-08-02 2003-08-12 Wacker-Chemie Gmbh Antifoam formulation
US6821943B2 (en) 2001-03-13 2004-11-23 S. C. Johnson & Son, Inc. Hard surface antimicrobial cleaner with residual antimicrobial effect comprising an organosilane
EP1565580A2 (en) * 2002-11-25 2005-08-24 Cepheid Compositions, methods and kits for polynucleotide amplification reactions and microfluidic devices
WO2005117611A1 (en) * 2004-06-03 2005-12-15 Wacker Chemie Ag Verfahren zur reduzierung des schaumens bei der wassrigen kartoffelverarbeitung sowie entschaumer
US7105581B2 (en) 2002-11-28 2006-09-12 Wacker-Chemie Gmbh Antifoam formulations
US7645360B2 (en) 2005-06-02 2010-01-12 Wacker Chemie Ag Defoamer formulations
DE102009028041A1 (en) 2009-07-27 2011-02-03 Wacker Chemie Ag defoamer
WO2011109319A1 (en) 2010-03-01 2011-09-09 The Procter & Gamble Company Dual-usage liquid laundry detergents
WO2011134746A1 (en) * 2010-04-28 2011-11-03 Wacker Chemie Ag Antifoam compositions
WO2016022786A1 (en) 2014-08-07 2016-02-11 The Procter & Gamble Company Soluble unit dose comprising a laundry detergent composition
WO2021076683A1 (en) 2019-10-15 2021-04-22 The Procter & Gamble Company Detergent compositions
WO2023180637A1 (en) 2022-03-21 2023-09-28 Elkem Silicones France Sas Concentrated silicone antifoam emulsion

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3691091A (en) * 1969-03-22 1972-09-12 Goldschmidt Ag Th Defoaming emulsion
US4395352A (en) * 1978-06-29 1983-07-26 Union Carbide Corporation High efficiency antifoam compositions and process for reducing foaming
EP0459512A2 (en) * 1990-06-01 1991-12-04 UNION CARBIDE CHEMICALS AND PLASTICS COMPANY INC. (a New York corporation) Organosilicone antifoam composition
CA2048823A1 (en) * 1990-08-08 1992-02-09 Dorset Industrial Chemicals Ltd. Defoamer
JPH07163806A (en) * 1993-12-13 1995-06-27 Shin Etsu Chem Co Ltd Composition for antifoam
US5431853A (en) * 1992-04-27 1995-07-11 Nikko Chemical Institute Inc. Modified silicone oil-in-water emulsion defoaming agent and defoaming method using it

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3691091A (en) * 1969-03-22 1972-09-12 Goldschmidt Ag Th Defoaming emulsion
US4395352A (en) * 1978-06-29 1983-07-26 Union Carbide Corporation High efficiency antifoam compositions and process for reducing foaming
EP0459512A2 (en) * 1990-06-01 1991-12-04 UNION CARBIDE CHEMICALS AND PLASTICS COMPANY INC. (a New York corporation) Organosilicone antifoam composition
CA2048823A1 (en) * 1990-08-08 1992-02-09 Dorset Industrial Chemicals Ltd. Defoamer
US5431853A (en) * 1992-04-27 1995-07-11 Nikko Chemical Institute Inc. Modified silicone oil-in-water emulsion defoaming agent and defoaming method using it
JPH07163806A (en) * 1993-12-13 1995-06-27 Shin Etsu Chem Co Ltd Composition for antifoam

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 9218, Derwent World Patents Index; Class A97, AN 92-141670, XP002042941 *
DATABASE WPI Section Ch Week 9534, Derwent World Patents Index; Class A26, AN 95-260142, XP002042466 *

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000036063A1 (en) * 1998-12-11 2000-06-22 Henkel Kommanditgesellschaft Auf Aktien Aqueous foam control emulsion
US6605183B1 (en) 1999-08-02 2003-08-12 Wacker-Chemie Gmbh Antifoam formulation
US6521586B1 (en) 1999-08-13 2003-02-18 Dow Corning S.A. Silicone foam control agent
US6521587B1 (en) 1999-08-13 2003-02-18 Dow Corning S.A. Silicone foam control agent
US6821943B2 (en) 2001-03-13 2004-11-23 S. C. Johnson & Son, Inc. Hard surface antimicrobial cleaner with residual antimicrobial effect comprising an organosilane
EP1565580A2 (en) * 2002-11-25 2005-08-24 Cepheid Compositions, methods and kits for polynucleotide amplification reactions and microfluidic devices
EP1565580A4 (en) * 2002-11-25 2007-04-25 Cepheid Compositions, methods and kits for polynucleotide amplification reactions and microfluidic devices
US7105581B2 (en) 2002-11-28 2006-09-12 Wacker-Chemie Gmbh Antifoam formulations
WO2005117611A1 (en) * 2004-06-03 2005-12-15 Wacker Chemie Ag Verfahren zur reduzierung des schaumens bei der wassrigen kartoffelverarbeitung sowie entschaumer
US7645360B2 (en) 2005-06-02 2010-01-12 Wacker Chemie Ag Defoamer formulations
DE102009028041A1 (en) 2009-07-27 2011-02-03 Wacker Chemie Ag defoamer
EP2289977A1 (en) 2009-07-27 2011-03-02 Wacker Chemie AG Defoamer formulations
US8222303B2 (en) 2009-07-27 2012-07-17 Wacker Chemie Ag Defoamer formulations
WO2011109319A1 (en) 2010-03-01 2011-09-09 The Procter & Gamble Company Dual-usage liquid laundry detergents
WO2011134746A1 (en) * 2010-04-28 2011-11-03 Wacker Chemie Ag Antifoam compositions
JP2013531550A (en) * 2010-04-28 2013-08-08 ワッカー ケミー アクチエンゲゼルシャフト Antifoam composition
US8530401B2 (en) 2010-04-28 2013-09-10 Wacker Chemie Ag Antifoam compositions comprising a mixture of organopolysiloxanes
WO2016022786A1 (en) 2014-08-07 2016-02-11 The Procter & Gamble Company Soluble unit dose comprising a laundry detergent composition
WO2021076683A1 (en) 2019-10-15 2021-04-22 The Procter & Gamble Company Detergent compositions
WO2023180637A1 (en) 2022-03-21 2023-09-28 Elkem Silicones France Sas Concentrated silicone antifoam emulsion

Also Published As

Publication number Publication date
AU3270097A (en) 1998-01-21

Similar Documents

Publication Publication Date Title
US4076648A (en) Self-dispersible antifoam compositions
WO1998000216A1 (en) Aqueous silicone defoaming agent
EP0121210B1 (en) Hydrocarbon oil based silicone antifoams
US5380464A (en) Silicone foam control composition
US5977191A (en) Method for controlling foam
CA2238225C (en) Water dispersible antifoam concentrates
US6207722B1 (en) Foam control compositions having resin-fillers
JP2007222812A (en) Defoaming agent composition
JPH01317505A (en) Silicone foaming control composition
WO2006063235A9 (en) Defoamer emulsion compositions for pulp mill applications
CN102197065A (en) Antifoaming compositions
CA1298528C (en) Foam control process for highly acidic aqueous systems
US7879917B2 (en) Defoamers for pulp and papermaking applications
JP4005170B2 (en) Dispersible silicone composition
JP3974845B2 (en) Antifoam composition
EP2325262A1 (en) Preparation of antifoaming oil compound and antifoam composition
JP3944689B2 (en) Antifoam composition
JP3668792B2 (en) Defoamer for kraft pulp manufacturing process
JP2003164707A (en) Higher alcohol oil-in-water type emulsion anti-foaming agent composition
EP1606034A2 (en) Stabilized foam control compositions for lubricating compositions and their use
JP2007054682A (en) Emulsion type defoaming agent
JP2003024708A (en) Defoaming agent composition
JP2004057872A (en) Defoaming agent composition
JP2003230804A (en) Method for stabilizing oil in water type silicone emulsion defoaming composition
JP2004008894A (en) Higher alcohol-based emulsion anti-foaming agent composition

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GE HU IL IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK TJ TM TR TT UA UG UZ VN

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE

121 Ep: the epo has been informed by wipo that ep was designated in this application
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWE Wipo information: entry into national phase

Ref document number: PA/A/1999/000233

Country of ref document: MX

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
NENP Non-entry into the national phase

Ref document number: 98503950

Country of ref document: JP

122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: CA