WO1996010602A1 - POLYMERS USEFUL AS pH RESPONSIVE THICKENERS AND MONOMERS THEREFOR - Google Patents
POLYMERS USEFUL AS pH RESPONSIVE THICKENERS AND MONOMERS THEREFOR Download PDFInfo
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- WO1996010602A1 WO1996010602A1 PCT/US1995/012601 US9512601W WO9610602A1 WO 1996010602 A1 WO1996010602 A1 WO 1996010602A1 US 9512601 W US9512601 W US 9512601W WO 9610602 A1 WO9610602 A1 WO 9610602A1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F20/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
- C07C69/54—Acrylic acid esters; Methacrylic acid esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/30—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety
- C08F220/302—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety and two or more oxygen atoms in the alcohol moiety
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/932—Thickener or dispersant for aqueous system
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- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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Abstract
Novel aqueous thickener or thixotropic polymers are prepared by the copolymerization of (A) about 15-60 weight percent of a C3-C8 alpha, beta-ethylenically unsaturated carboxylic acid monomer, preferably acrylic or methacrylic acid or a mixture thereof with itaconic or fumaric acid, (B) about 15-80 weight percent of a nonionic copolymerizable C2-C12 alpha, beta-ethylenically unsaturated monomer, preferably a monovinyl ester such as ethyl acrylate or a mixture thereof with styrene, acrylonitrile, vinyl chloride or vinyl acetate, and (C) about 1-30 weight percent of a new and novel nonionic ethylenically unsaturated nonionic biphillic monomer such as tristyrylpoly(ethyleneoxy)x methyl acrylate, to provide a stable aqueous colloidal dispersion at an acid pH lower than about 5.0 but becoming an effective thickener for aqueous systems upon adjustment to a pH of about 5.5-10.5 or higher. These polymers adjusted to a pH of about 5.5 or higher are effective thickeners for a wide variety of aqueous systems including cosmetic products, drilling muds, aqueous coating compositions such as latex paint, and high solids compositions such as spackle, grouts, cements, and the like.
Description
POLYMERS USEFUL AS pH RESPONSIVE THICKENERS AND MONOMERS THEREFOR
BACKGROUND OF THE INVENTION
Polymeric water-soluble thickening agents have been extensively used for thickening aqueous based systems containing electrolytes or a dispersed phase including coatings, e.g., latex paints, printing pastes for textiles, bleaching agents, alkaline liquors or paint removers as well as high solids content products like spackle, cements, grout and the like. Further important applications relate to the production of petroleum and ores, as filtration aids or flocculents, and found use in working fluids such as hydraulic fluids and metal working fluids.
In aqueous coating compositions, such as latex paints, it is important to control the rheology to obtain proper flow and leveling with a minimum of dripping and spattering. In other compositions Newtonian flow thickeners are required because of the high shear involved in their use.
Cellulose ethers, alkali soluble latex copolymers, copolymers of acrylic and methacrylic acids and esters which have a portion of the hydrogen ions of the copolymer carboxyl groups replaced with ammonium or alkali metal ions have been used as thickeners as well as other types of polymeric thickeners which contain various carboxylic acid groups which can be solubilized in water by neutralization with a water-soluble base.
A solid styrene-maleic anhydride-vinylbenzyl ether terpolymer soluble at high pH and useful as a thickener for aqueous solutions, in spite of excellent rheology, has had limited use as a paint thickener because of stability problems and cost. U.S. Patent No. 4,384,096 discloses a pH responsive thickener comprising an ethylenically unsaturated carboxylic acid, at least one ethylenically unsaturate monomer, and an ethylenically unsaturated surfactant copolymerizable therewith. The surfactant is an alkylphenoxypoly(ethyleneoxy)ethyl acrylate. Similar systems are disclosed in U.S. Patent Nos. 4, 138,381 ;4,268,641; 4,668,410; 4,769,167; 5,086, 142; and 5,192,592.
It is also known that water soluble polymers of the same type as disclose in the preceding patents can be used in the formulation of synthetic and semi-syntheti hydraulic fluids to adjust the viscosity to the proper level to achieve technic requirements. See U.S. Patent Nos. 4,668,410 and 4,769,167. SUMMARY OF THE INVENTION
In accordance with the invention, there is provided a new and nov copolymerizable nonionic ethylenically unsaturated biphillic monomer which can be use in preparing stable liquid emulsion or solution polymers having low viscosity an relatively high solids content under acidic conditions which become very efficie polymeric thickeners for many aqueous systems when treated with base. These ne polymers, which surprising develop maximum viscosity at lower pHs than simila products presently available in the prior art, can be prepared in the form of an aqueou colloidal dispersion of water-insoluble polymer by emulsion polymerizing at a Ph of abo 2.5 to 5.0 three ethylenically unsaturated monomeric components: (A) a carboxylic aci monomer, (B) a nonionic vinyl monomer and (C) the novel nonionic ethylenicall unsaturated biphillic monomer of the invention.
The emulsion polymerization is normally carried out under acidi conditions in which the carboxylic acid groups are in protonated form to insolubilize th polymer and give a liquid emulsion. The finely divided polymer particles in such a liqui colloidal dispersion dissolve almost instantly upon pH adjustment. The ease of handling metering, and dispersing the liquid emulsion polymer, the rapid solubilization b controlled pH adjustment, and the highly desirable Theological properties make this liqui emulsion polymer a most effective and efficient thickening agent for a wide variety o applications including latex paints and other aqueous coating and heavy solid compositions.
DETAILED DESCRIPTION OF THE INVENTION
The novel liquid emulsion polymers of this invention are prepared from three basic components: (A) an C3-C8 alpha, beta -ethylenically unsaturated carboxylic acid monomer, (B) a copolymerizable nonionic vinyl monomer, and (C) certain new and novel copolymerizable nonionic ethylenically unsaturated biphillic monomers. The effectiveness of these liquid emulsion polymers as a pH responsive thickener for many aqueous products is dependent on these components in that the acid component A provides the requisite pH responsiveness; the nonionic vinyl comonomer B provides an extended polymer backbone and added hydrophilic lipophilic balance; and the novel ethylenically unsaturated nonionic biphillic monomers C provides an in situ, bound surfactant to control the rheology of the aqueous system containing the solubilized polymeric thickener. The proportions of the individual monomers can be varied to achieve optimum properties for specific applications.
The new and novel copolymerizable ethylenically unsaturated nonionic surfactant of the invention can be represented by the formula:
FORMULA I where R is H or CH3; R, is C,-C4 alkyl; n is an average number from about 6-100 and m is an average number from about 0-50 provided that n is > or = m and SIGMA (n
-I- m) is about 6-100, and x is an average number of from about 2 to about 3, wherein the substituent denoted x is randomly distributed around the benzene ring to which it is
attached.
The preferred surfactants are the acrylate and methacrylate esters wh include (1 -phenyl ethyl),, phenyl poly (alkyleneoxy) (meth)acrylates where x is a num of from about 2-3, and the poly (alkyleneoxy) moiety is preferably ethyleneoxy thoug can be ethyleneoxy and/or propyleneoxy, the repeating alkyleneoxy units being a num average of from about 6-100. An alternate name for the (1-phenyl ethyl) phenyl gr is the mono, di or tristyrylphenol.
The new and novel ethylenically unsaturated nonionic biphillic monom of the invention are the acrylic or methacrylic acid esters of certain nonionic surfact alcohols. Such surfactant alcohols are known in the art, e.g. U.S. 5,082,591. alcohols can be prepared by alkoxylating a styrylphenol by known methods. example, the alcohols can be prepared by the reaction of at least one poly(l -phe ethyl), phenol wherein x is an average of 2-3 with a mixture of monoethylene glycol a monopropylene glycol. If organic solvent solubility is desired, the ratio of monoethylene glycol to monopropylene glycol ranging from about 75/25 to 90/10 a preferably from about 80/20 to 90/10 is taught as necessary. This is more fully disclo in U.S. Patent No. 5,082,591, the disclosure of which is incorporated herein reference.
The reaction can be carried out for a period of time sufficient for reacti e.g., from about 20 to 40 minutes, at a temperature ranging from about 140" to 180" in the presence of from about 0.5 to 1.5 % by weight with respect to the finished prod
of an alkaline base, such as soda, as a catalyst. The (1 -phenyl ethyl)x phenol together with the glycol (s) are used in substantially stoichiometnc amounts. Variations in reaction conditions would be obvious to one of ordinary skill in the art as would other methods of preparing the compounds of the invention. Additional surfactant alcohols which can be esterified for use herein are given in "McCutcheon's Detergents and Emulsifiers"
1973, North American Edition, Allured Publishing Corp., Ridge wood, NJ. 07450 under the trademark SOPROPHOR offered by Rhone-Poulenc.
The tristyrylphenol alkoxylate can then be esterified with an ethylenically unsaturated carboxylic acid or its anhydride by known methods to obtain the desired product, e.g., U.S. Patent No. 4,075,411.
The novel surfactants of the invention can be prepared by the direct acid catalyzed esterification of the appropriate surfactant alcohol with an excess of the carboxylic acid monomer used as Component A in the formation of the final polymer. The resulting mixture with excess acid can be used directly in the copolymerization provided that at least 30 percent, and preferably 50-70 percent or more, of the surfactant alcohol in the mixture is esterified. The novel surfactants of the invention can also be recovered, purified by conventional means using an appropriate inhibitor such as hydroquinone or p-tert-butylcatechol to prevent undesired homopolymerization, and then used to prepare the liquid emulsion polymers.
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It has been found that the hydrophilic lipophilic balance (HLB) of the nove surfactants of the invention is an important factor in the performance of the resultin emulsion polymer. Thus for a given polyethyleneoxy content, increasing the molecula weight of the terminal hydrophobic group will increase the efficiency of the resultin polymer as a thickener. Also for a given lipophilic group decreasing the number o polyethyleneoxy groups increases thickener efficiency. For many surfactant esters usabl herein an average of about 10-40 ethyleneoxy groups (e.g., In Formula I, m = 0, an n = 10-40) is preferred.
The ethylenically unsaturated nonionic biphillic monomer is generally use in the copolymer in an amount ranging from about 1 to about 30 (preferably from abou
1-20, and more preferably from about 1-12) weight percent based on the total weight o the monomers present.
The liquid emulsion polymer requires from about 15-60 weight percen based on total monomers of a C3-C8 alpha, beta -ethylenically unsaturated carboxylic aci monomer of the formula:
FORMULA II RCH=C(R,) - C(O)OH where when (a) R is H then R, is H, CrC4 alkyl, or -CH2C(O)OX; (b) R is -C(O)OX then R, is H or -CH2C(O)OX; or R is CH3 then R, is H; and X is H or C,-C4 alkyl.
Acrylic or methacrylic acid or a mixture thereof is preferred though these acids can be used with minor proportions of itaconic or fumaric acid, crotonic and
aconitic acid and half esters of these and other polycarboxylic acids such as maleic acid with C]-C4 alkanols. It is preferable to have at least about 25 weight percent, more preferably from about 30-55 and most preferably from about 30-45 weight percent of the carboxylic acid monomer in the polymer though polycarboxylic acid monomers and half esters can be substituted for a portion of the acrylic or methacrylic acid, e.g., about 1-15 weight percent based on total monomers.
To provide the extended polymer backbone and body needed for effective thickening requires about 15-80 weight percent of at least one copolymerizable nonionic C2-C,2 alpha, beta-ethylenically unsaturated monomer selected from the group consisting of the formula:
FORMULA ID CH2=CYZ wherein when Y is H then Z is -COOR', -CAR". CN, Cl, -OC(O)R"' or -CH=CH2; when Y is CH3 then Z is -COOR', - H4R", CN or -CH=CH2; or when Y is Cl then Z is Cl; and R' is C,-C8 alkyl or C2-C8 hydroxyalkyl; R" is H, Cl, Br, or C,-C4 alkyl; R"' is CrC8 alkyl.
Typical of such monomers are the Cι-C8 alkyl and C2-C8 hydroxyalkyl esters of acrylic and methacrylic acid including ethyl acrylate, ethyl methacrylate, methyl methacrylate, 2-ethylhexyl acrylate, butyl acrylate, butyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxybutyl methacrylate; styrene, vinyltoluene,
t-butylstyrene, isopropylstyrene, and p-chlorostyrene; vinyl acetate, vinyl butyrate, vin caprolate; acrylonitrile, methacrylonitrile, butadiene, isoprene, vinyl chloride, vinylide chloride, and the like. In practice, a monovinyl ester such as ethyl acrylate or a mixtu thereof with styrene, hydroxyethyl acrylate, acrylonitrile, vinyl chloride or vinyl aceta is preferred.
Normally from about 15-80 weight percent, and preferably from about 3 70 and more preferably from about 50-70 weight percent of nonionic vinyl monome based on total weight of monomers, is used in preparing the liquid emulsion polymer. The hydrophilic balance of the copolymer product can be adjusted to degree by the judicious selection of the nonionic vinyl monomer B; e.g. , a soft, (1-phen ethyl) phenylpoly(ethyleneoxy)ethyl ester can be used in a system with mixture of eth acrylate and a hard co onomer such as styrene. It is critical to the performance of thes products that they contain an effective amount of an in situ, bound surfactant to contr the rheology of the aqueous system thickened with the solubilized emulsion polymer. 2. Copolymerization
The liquid emulsion copolymers of the invention can be convenientl prepared from the above-described monomers by conventional emulsion polymerizatio techniques at an acid pH lower than about 5.0 using free-radical producing initiator usually in an amount from 0.01 percent to 3 percent based on the weight of th monomers. Polymerization at an acid pH lower than about 5.0 permits direct preparatio
of an aqueous colloidal dispersion with relatively high solids content without problems of undue viscosity. The free-radical producing initiators conveniently are peroxygen compounds especially inorganic persulfate compounds such as ammonium persulfate, potassium persulfate, sodium persulfate; peroxides such as hydrogen peroxide; organic hydroperoxides, for example, cumene hydroperoxide, t-butyl hydroperoxide; organic peroxides, for example, benzoyl peroxide, acetyl peroxide, lauroyl peroxide, peracetic acid, and perbenzoic acid (sometimes activated by a water-soluble reducing agent such as ferrous compound or sodium bisulfite); as well as other free-radical producing materials such as 2,2'-azobisisobutyronitrile and high radiation sources. Optionally, a chain transfer agent and an additional emulsifier can be used.
Representative chain transfer agents are carbon tetrachloride, bromoform, bromotrichloromethane, long chain alkyl mercaptans and thioesters such as n-dodecyl mercaptan, t-dodecyl mercaptan, octyl mercaptan, tetradecyl mercaptan, hexadecyl mercaptan, butyl thioglycolate, isooctyl thioglycolate, and dodecyl thioglycolate. The chain transfer agents can be used in amounts up to about 10 parts per
100 parts of polymerizable monomers.
At least one anionic emulsifier can also be included in the polymerization charge and one or more of the known nonionic emulsifiers may also be present. Examples of anionic emulsifiers are the alkali metal alkyl aryl sulfonates, the alkali metal alkyl sulfates and the sulfonated alkyl esters. Specific examples of these well-known
emulsifiers are sodium dodecylbenzenesulfonate, sodium disecondary-butylnaphthalen sulfonate, sodium lauryl sulfate, disodium dodecyldiphenyl ether disulfonate, disodiu n-octadecylsulfosuccinamate and sodium dioctylsulfosuccinate.
Optionally, other ingredients well known in the emulsion polymerizatio art may be included such as chelating agents, buffering agents, inorganic salts and p adjusting agents.
Usually the copolymerization is carried out at a temperature between abou 60° C. and 90°C. but higher or lower temperatures may be used. The polymerization ca be carried out batchwise, stepwise or continuously with batch and/or continuous additio of the monomers in a conventional manner.
The monomers can be copolymerized in such proportions, and the resultin emulsion polymers can be physically blended, to give products with the desired balanc of properties for specific applications. For example, if a more viscous product is desired the acid and surfactant monomer content can be increased. Greater flexibility an coalescence can be obtained with higher amounts of ethyl acrylate. Addition of styren as a second nonionic vinyl monomer will increase to a higher pH the adjustment require to dissolve the emulsion in an aqueous coating composition. Minor quantities of polyfunctional monomer, such as itaconic or fumaric acid or isoprene to introduce higher carboxylic acid content or limited crosslinking, provides further control on th solubility of the emulsion polymer after pH adjustment. Thus, by varying the monomer
and their proportions, emulsion polymers having optimum properties for particular applications can be designed. Particularly effective liquid emulsion polymer thickeners are obtained by copolymerization of about 40-50 weight percent of methacrylic acid, about 35-50 weight percent of ethyl acrylate, and about 1-12 weight percent of the methacrylic ester of a C9-alkylphenoxy (ethyleneoxy), ethyl alcohol.
As the tristyrylethoxylate methacrylates of the inveniton have increased chain transfer ability, it may be desirable to add a polyfunctional monomer, e.g., diallyl phthalate, and closely control the polymerization to increase viscosity.
The copolymer products prepared by emulsion polymerization at an acid pH are in the form of stable aqueous colloidal dispersions containing the copolymer dispersed as discrete particles having average particle diameters of about 500-3000 A, preferably about 1000-1750 A, as measured by light refraction. Dispersions containing polymer particles smaller than about 500 A are difficult to stabilize while particles larger than about 3000 A reduce the ease of dispersion in the aqueous products to be thickened.
5 These emulsion copolymers will normally have number average molecular weights of at least about 30,000 daltons as determined by gel permeation chromatography. To provide most effective thickening with copolymers which are water-soluble when neutralized, molecular weights within the range of about 200,000 to 5,000,000 daltons are preferred. In terms of a standard Brookfield viscosity measured as
) a 1 percent aqueous solution in ammonium salt form at pH 9 and 25* C, a copolymer
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with a viscosity of about 50-50,000 cps, and preferably about 100-30,000 cps, particularly desirable for many applications. The aqueous dispersions of the copolym contain about 10-50 weight percent of polymer solids and are of relatively low viscos They can be readily metered and blended with aqueous product systems. The dispersions are pH responsive. When the pH of the polymer dispers is adjusted by addition of a base such as ammonia, an amine or a non-volatile inorga base such as sodium hydroxide, potassium carbonate or the like, the aqueous mixt becomes translucent or transparent as the polymer dissolves at least partially in aqueous phase with a concurrent increase in viscosity. This neutralization can occur in situ when the liquid emulsion polyme blended with an aqueous solution containing a suitable base. Or if desired for a gi application, pH adjustment by partial or complete neutralization can be carried out bef or after blending the liquid emulsion polymer with an aqueous product.
The term "liquid emulsion polymer" as applied to the new thickener of t specification means that the thickener is an emulsion polymer because the polymer prepared by emulsion polymerization even though the polymer per se may be ( generally is) a solid at room temperature but is a "liquid" emulsion polymer becaus is in the form of a liquid solution or dispersion.
The pH viscosity response curves for several typical liquid emulsion polymers prepared by copolymerizing methacrylic acid (MAA), ethyl acrylate (EA), and nonylphenoxypoly(ethyleneoxy)9ethyl methacrylate (VSE-IA) are shown in the FIGURE as determined in aqueous media at a concentration of 1 percent by weight and at room temperature. Note that the pH range of initial viscosity build can be controlled by variation in the composition of the emulsion copolymer.
Polymers can also be made using solution polymerization techniques well known to those of skill in the art. The monomers can be dissolved in an appropriate solvent such as toluene, xylene and tetrahydro furan. Polymerization can be accomplised in the time and at the temperature necessary, e.g., 60"- 80* C. and 8-24 hours. The product can be worked up through normal techniques including solvent stripping.
The polymers prepared in accordance with the invention are useful as water-soluble thickeners for a wide variety of applications ranging from cosmetics to drilling muds, but particularly for aqueous coating compositions. Solution polymerized polymers can be used in solvent systems or emulsified by known techniques for use in aqueous systems.
The liquid emulsion polymers described herein are particularly useful as thickeners for a wide variety of water-based compositions including aqueous brine and polymer solutions as well as aqueous slurries and colloidal dispersions of water-insoluble inorganic and organic material including compositions such as natural rubber, synthetic
or artificial latexes and aqueous products containing such materials. The emulsi polymers of the invention are especially useful in areas requiring thickening at pHs ne neutral such as in cosmetics. The compositions of the invention can provide substantial maximum thickening at neutral pH whereas many of the compositions of the prior require alkaline pH for maximum thichening.
Synthetic latexes which may be thickened with the liquid emulsi polymers are aqueous colloidal dispersions of water-insoluble polymers prepared emulsion polymerization of one or more ethylenically unsaturated monomers. Typical such synthetic latexes are emulsion copolymers of monoethylenically unsaturated compounds such as styrene, methyl methacrylate, acrylonitrile with conjugated diolefin such as butadiene or isoprene; copolymers of styrene, acrylic a methacrylic esters, copolymers of vinyl halide, vinylidene halide, vinyl acetate and t like. Many other ethylenically unsaturated monomers or mixtures thereof can be emulsion polymerized to form synthetic latexes. The thickeners of this invention are advantageous for use with t water-based compositions according to the foregoing description and with compositio containing those materials, especially coating compositions of various types. Mixtures two or more thickeners may be used, if desired. Of course the latex polymers used coating compositions are preferably film-forming at temperatures below about 25 °C,
either inherently or through the use of plasticizers. Such coating compositions include water-based consumer and industrial paints; sizing, adhesives and other coatings for paper, paperboard, textiles; and the like.
Usually these latex coating compositions contain added pigments, fillers and extenders such as titanium dioxide, barium sulfate, calcium carbonate, clays, mica, talc, silica and the like. The novel liquid emulsion polymers described herein are compatible with most latex paint systems and provide highly effective and efficient thickening. Suitable results are obtained using about 0.05-5.0 weight percent of the liquid emulsion polymer based on total weight of solids, and preferably about 0J-2.0 weight percent.
The aqueous compositions thickened with the liquid emulsion polymers of this invention preferably are those in which any dispersing or solvating liquid present consists of greater than 50 percent by weight of water.
The following examples illustrate further the present invention. Unless otherwise indicated, all parts and percentages are by weight.
EXAMPLE 1 Preparation of Tristyrylphenol Ethoxylate
Typically tristyrylphenyl ethoxylate can be prepared by reacting tristyrylphenol and soda with monoethylene &/or monopropylene glycol at a temperature
) and time sufficient to allow alkoxylation, e.g., 160* C. for about 30 minutes. The
tristyrylphonol and the monoalkylene glycols are used in stoichiometnc amounts, the rati of ethylene to propylene glycol being that desired for the final desired ratio. Th tristryrlphenol as used is a mixture of mono, di and tristyryl compounds with the tristyr moiety prevailing. Preparation of Biphillic Monomer 1A
The following is a procedure for the preparation of the ethylenicall unsaturated nonionic biphillic monomer of the invention.
The biphillic monomer can be prepared by charging a 3 liter four nec round bottom flask equipped with a heater, thermometer, subsurface air sparge (abo 100 milliliters/ minute), an addition funnel, and a stirrer with 1508.04 grams o tristyrylphenol ethoxylate (EO = 25) available as SOPROPHOR S/25 from Rhόn Poulenc Inc. which had been previously liquified in a 60* C. oven. 500 ppm meth hydroquinone was also charged at that point. The water content was maintained at les than 0J % . The temperature was elevated to about 60* C. with air sparging and stirring 154.17 grams of methacrylic anhydride was incrementally added maintaining the reactio temperature between 60* and 90* C. After addition was completed, samples wer analyzed until the IR peak at 1780 cm*1 corresponding to methacrylic anhydride wa minimized and the acid number was stable. The final product, 1576.11 grams, wa stored in an amber jar.
Preparation of Biphillic Monomer IB
The biphillic monomer IB can be prepared by charging a 1 liter four neck round bottom flask equipped with a heater, thermometer, subsurface air sparge (about
100 milliliters/ minute), an addition funnel, and a stirrer with 500 grams of tristyrylphenol ethoxylate (EO = 16) available as SOPROPHOR 37 from Rhόne-Poulenc Inc. and 500 ppm methyl hydroquinone. The water content was maintained at less than 0.1 %. At a temperature of about 25* C. with air sparging and stirring, 84.42 grams of methacrylic anhydride was incrementally added. No increase in reaction temperature was noted.
After addition was complete, the temperature was elevated to 50* C. Samples were analyzed until the methacrylic anhydride was minimized and the acid number was stable
(about 12 hours). The final product was cooled and stored in an amber jar.
Preparation of Biphillic Monomer 1C
The process used to prepare sample 1C was repeated using 301 grams of tristyrylphenol ethoxylate (EO = 40) available as SOPROPHOR 40 from Rhόne-Poulenc Inc. and 105.9 grams of methacrylic acid.
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EXAMPLE 2
An emulsion polymer utilizing the biphillic monomer of the invention w prepared as follows.
An emulsion of monomers was prepared by mixing 153.4 grams of eth acrylate, 100.9 grams of methacrylic acid, 6.6 grams of a solution containing 58.9 weig
% of the monomer prepared in Example 1, 20 weight % methacrylic acid and 20 weig
% water, 12.0 grams of Abex EP 100 (nonylphenol polyethoxylate ammonium salt), 0. grams of diallyl phthalate and 150 grams of deionized water.
To a one liter externally heated/cooled glass reactor equipped with a agitator and feed pumps were added 291 grams of deionized water and 1.0 grams
Abex EP 100 under a nitrogen blanket. The vessel was heated to 84-86* C. and 1 grams of the above described emulsion and 2.5 grams of a 0.56% solution of ammoniu persulfate was added. After evidence of polymerization was noted (0.5 to 2.0 minutes the remaining monomer emulsion along with 30 grams of a 1.27% solution of ammoniu persulfate was added incrementally over 90 minutes. The reaction temperature wa maintained at 84-86* C. with external cooling. After the addition of the reactants, th reactor was heated to 90* C. for 30 minutes. The reactor was then cooled to 62-64* and 30 grams of a 1.8% aqueous solution of t-butyl hydroperoxide and 30 grams of
0.36% aqueous solution of erythorbic acid was added in three equal increments 2 minutes apart. The reactor temperature was held at 63-65* C. for 45 minutes. Th
resultant latex was filtered through a 250 mesh screen and then a 325 mesh screen to provide a polymer emulsion containing approximately 59% ethyl acrylate, 39.35% methacrylic acid, 1.5% biphillic monomer and 0.15% diallyl phthalate.
The latex was subsequestly neutralized and dissolved to 1 % solids by weight. The transformation from a lates to a medium viscosity clear solution occurred near pH6 and maximum viscosity was obtained at about pH 7.5.
Other polymers were prepared using the same procedure with the following monomer charges:
Sample Ethyl Methacrylic Biphillic Diallyl Acrylate Acid of Example 1 Phthalate
A. 59% 36.00% 5.0% (IA)
B. 59% 38.00% 3.0% (IA)
C. 59% 39.35% 1.5% (IB) 0J5 D. 59% 36.00% 5.0% (IC)
EXAMPLE 3 The thixotropic behavior of aqueous solutions of copolymers prepared using the biphillic monomer of the invention can be shown by the following:
To a 250 milliliter beaker equipped with a magnetic stirrer are added 6.67 grams of a 30% solids latex and 191.88 grams of deionized water. 1.35 grams of caustic (25% NaOH) was added dropwise until the desired pH was attained (by pH meter). When the solution clears and is at the desired pH (pH 7-7.5), the solution is stirred at
25* C. for about 2 hours to insure uniformity. The viscosity is determined with a mod LVT Brookfield Viscometer using a # 3, 4, or 5 spindle at 3, 6, 12, 30, and 60 RP The following results were obtained:
Sample 3A - 59% ethyl acrylate, 39.35% methacrylic anhydride, 1.5 tristyrylphenol (ethoxylate)^ methacrylate and 0.15% diallyl phthalate.
TABLE pH 3 RPM 6 RPM 12 RPM 30 RPM 60 RPM
7.06 10998 6199 3749 2020 1270 8.04 8998 5599 3499 1960 1280
9.36 8798 5499 3399 1907 1220
Sample 3B - 59% ethyl acrylate, 36% methacrylic acid, 5 tristyrylphenol (ethoxylate)x methacrylate at a pH of about 7: x 6 RPM 12 RPM 30 RPM 60 RPM
16 2100 1670 1044 728
25 2060 1580 1052 746 A latex was prepared according to the process outlined in Example 2 usin a behenyl ethoxylat--^ methacrylate(BEM) or a tristyrylphenol ethoxylate^ methacrylate The thickening ability of 1 % solutions at a pH of about 7 were compared using th procedure outlined hereinbefore with the following results:
MONOMER 6 RPM 12 RPM 30 RPM 60 RPM
Inv. x = 25 4439 2779 1540 1002
BEM 1340 1410 1520 1424
Additional advantages and modifications will be readily apparent to those skilled in the art. Accordingly, variations can be made without departing from the spirit and general inventive concept as defined in the appended claims and their equivalents.
Claims
1. An ethylenically unsaturated biphillic monomer of the formula:
FORMULA I wherein R and R, represent hydrogen or methyl, n is an average number from about to about 100, m is an average number of from about 0-50 provided that n is > or = and SIGMA (m + n) is an average number from about 6-100, and x is an averag number of from about 2 to about 3, wherein the substituent denoted by x is randoml distributed around the benzene ring to which it is attached.
2. An ethylenically unsaturated biphillic monomer as recited in claim wherein m is 0 and n ranges from about 6-50.
3. An ethylenically unsaturated biphillic monomer as recited in claim wherein m ranges from about 1-40 and n ranges from about 6-50.
4. An ethylenically unsaturated biphillic monomer as recited in claim wherein m is 0 and R is methyl.
5. An ethylenically unsaturated biphillic monomer as recited in claim 4 wherein n ranges from about 6-50.
6. A liquid emulsion polymer useful as a pH responsive thickener for aqueous compositions comprising an aqueous emulsion copolymer of:
A. about 15-60 weight percent based on total monomers of at least one -Cg ethylenically unsaturated carboxylic acid monomer;
B. about 15-80 weight percent of at least one nonionic, copolymerizable C2-C12 alpha, beta-ethylenically unsaturated monomer of the formula: Formula m. CH2=CYZ wherein when Y is H, Z is -COOR', -C^R", CN, Cl, -OC(O)RB' or -CH=CH2; Y is CH3, Z is -COOR', -C^R", CN or -CH=CH2; or Y and Z are Cl; and R' is C,-C„ alkyl or C2-C8 hydroxyalkyl; R" is H, Cl, Br, or C,-C4 alkyl; and R"' is C,-C8 alkyl; and C. about 1-30 weight percent based on total monomers of at least one nonionic ethylenically unsaturated biphillic monomer of the formula:
wherein R and R, represent hydrogen or methyl, n is an average number from about to about 100, m is an average number of from about 0-50 provided that n is > or = and SIGMA (m + n) is an average number from about 6-100, and x is an averag number of from about 2 to about 3, wherein the substituent denoted by x is randoml distributed around the benzene ring to which it is attached, said polymer being stable an aqueous colloidal dispersion at a pH lower than about 5.0 but becoming an effectiv thickener for aqueous systems upon adjustment to a pH of about 5.5-10.5 or higher.
7. A polymer of claim 6 where the carboxylic acid monomer (A) methacrylic acid, acrylic acid, or a mixture thereof with fumaric or itaconic acid.
8. A polymer of claim 6 containing about 30-55 weight percent methacrylic acid or a mixture thereof with a minor amount of itaconic acid.
9. A polymer of claim 6 where the comonomer (B) is a monovinyl ester o a mixture thereof with styrene, 2-hydroxyethyl acrylate, acrylonitrile, vinyl chloride o
vinyl acetate.
10. A polymer of claim 6 where the comonomer (B) is ethyl acrylate.
11. A polymer of claim 6 where the amount of the carboxylic acid monomer (A) ranges from about 25 weight percent to about 60 weight percent.
12. A polymer of claim 6 where m is 0 and R is methyl.
13. A polymer of claim 12 where n ranges from 6-50.
14. A polymer of claim 6 comprising:
A. about 30-55 weight percent of methacrylic acid, acrylic acid or mixtures thereof with fumaric or itaconic acid;
B. about 35-70 weight percent of ethyl acrylate or mixtures thereof with styrene, 2-hydroxyethyl acrylate, acrylonitrile, vinyl chloride or vinyl acetate; and
C. about 1-20 weight percent of the ethylenically unsaturated biphillic monomer of claim 1.
15. The polymer of claim 6 comprising:
A. about 30-45 weight percent of methacrylic acid;
B. about 50-70 weight percent of ethyl acrylate; and
C. about 1-12 weight percent of the compound of Formula I.
16. A polymer of claim 6 having an average particle size of about 500-3 A and a Brookfield viscosity of about 50-50,000 cps as a 1 percent aqueous solutio ammonium salt form at pH 9.0 and 25* C.
17. A liquid aqueous colloidal dispersion useful as a pH responsive polym thickener for aqueous compositions and containing about 10-50 weight percent of polymer of claim 6 and having a pH of about 2.5-5.0.
18. The liquid aqueous colloidal dispersion of claim 17 where the poly consists essentially of:
A. about 30-45 weight percent of methacrylic acid;
B. about 50-70 weight percent of ethyl acrylate; and
C. about 1-12 weight percent of the compound of Formula I where m is 0 and about 6-40.
19. A process for making the liquid aqueous colloidal dispersion of clai comprising emulsion copolymerizing the monomeric mixture at a pH of about 2.5-5. the presence of a free-radical producing initiator at a temperature between about 60* -
C.
-26-
20. A process of claim 19 wherein the emulsion copolymerization gives a polymer having an average particle size of about 500-3000 A and a Brookfield viscosity of about 50-50,000 cps as a 1 percent aqueous solution in ammonium salt form at pH 9.0 and 25* C.
21. A process of claim 18 wherein the monomeric mixture comprises:
A. about 30-45 weight percent of methacrylic acid;
B. about 50-70 weight percent of ethyl acrylate or a mixture thereof with styrene, 2-hydroxyethyl acrylate, acrylonitrile, vinyl chloride, or vinyl acetate; and C. about 1-12 weight percent of the Compound of Formula I where m is 0 and n is about 6-100.
22. A thickened aqueous composition having a pH within the range of about 6.5-11.0 comprising an aqueous composition containing a water-soluble or dispersible material and an effective amount of a liquid emulsion polymer of claim 6.
23. A thickened aqueous composition of claim 21 wherein the aqueous composition is a colloidal dispersion of a water-insoluble polymer.
24. The thickened aqueous composition of claim 21 wherein the liq emulsion polymer comprising:
A. about 30-45 weight percent of methacrylic acid;
B. about 50-70 weight percent of ethyl acrylate; and C. about 1-12 weight percent of the Compound of Formula I where m is 0 and about 6-40.
25. A process for making a thickened aqueous composition which compris
(1) blending with the aqueous composition a sufficient amount of the liquid emuls polymer of claim 6 to thicken the aqueous coating composition and
(2) adjusting the pH of said blend within a range of about 6.5-11.0 as necessary dissolve the emulsion polymer therein and thus thicken the aqueous composition.
26. The process of claim 25 wherein the aqueous composition is a colloi dispersion of a water-insoluble polymer.
27. The process of claim 25 wherein the liquid emulsion polymer comprises:
A. about 30-45 weight percent of methacrylic acid;
B. about 50-70 weight percent of ethyl acrylate; and
C. about 1-12 weight percent of the Formula I where m is 0 and n is about 6-100.
Priority Applications (2)
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JP51209196A JP4290761B2 (en) | 1994-10-03 | 1995-09-29 | Polymers useful as pH-responsive thickeners and monomers therefor |
CA002200759A CA2200759C (en) | 1994-10-03 | 1995-09-29 | Polymers useful as ph responsive thickeners and monomers therefor |
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Application Number | Priority Date | Filing Date | Title |
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US31726194A | 1994-10-03 | 1994-10-03 | |
US08/317,261 | 1994-10-03 |
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WO1996010602A1 true WO1996010602A1 (en) | 1996-04-11 |
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PCT/US1995/012601 WO1996010602A1 (en) | 1994-10-03 | 1995-09-29 | POLYMERS USEFUL AS pH RESPONSIVE THICKENERS AND MONOMERS THEREFOR |
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US (2) | US5874495A (en) |
EP (1) | EP0705854B2 (en) |
JP (1) | JP4290761B2 (en) |
AT (1) | ATE165104T1 (en) |
CA (1) | CA2200759C (en) |
DE (1) | DE69502067T3 (en) |
DK (1) | DK0705854T3 (en) |
ES (1) | ES2118514T3 (en) |
FI (1) | FI954670A (en) |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11104479A (en) * | 1997-07-18 | 1999-04-20 | Coatex Sa | Use of surface active structural copolymer as dispersant and/or grinding assistant |
Families Citing this family (129)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5863975A (en) * | 1995-10-03 | 1999-01-26 | Rheox Inc. | Aqueous construction compositions with improved water retention properties and a process for providing water retention properties to aqueous construction compositions |
US6166112A (en) † | 1997-03-10 | 2000-12-26 | Nippon Shokubai Co., Ltd. | Cement admixture and cement composition |
FR2767327B1 (en) * | 1997-08-14 | 1999-10-29 | Atochem Elf Sa | NOVEL ASSOCIATIVE POLYMERS AND THEIR REVERSE EMULSION PREPARATION PROCESS |
FR2773159B1 (en) * | 1997-12-29 | 2000-03-24 | Rhodia Chimie Sa | ASSOCIATIVE DIOL ALKALISOLUBLE COPOLYMER AND ITS USE AS A THICKENER FOR PAPER COATING |
US6242527B1 (en) * | 1998-12-02 | 2001-06-05 | E. I. Du Pont De Nemours And Company | Solid surface materials derived from aqueous latex dispersions of thermoplastic polymers |
US6287418B1 (en) | 1999-01-25 | 2001-09-11 | Kimberly-Clark Worldwide, Inc. | Modified vinyl polymers containing amphiphilic hydrocarbon moieties |
CO5180563A1 (en) | 1999-01-25 | 2002-07-30 | Kimberly Clark Co | MODIFIED VINYL POLYMERS CONTAINING MEANS OF HYPHROCARBON HYDROCARBON AND THE METHOD FOR MANUFACTURING |
US6224714B1 (en) | 1999-01-25 | 2001-05-01 | Kimberly-Clark Worldwide, Inc. | Synthetic polymers having hydrogen bonding capability and containing polysiloxane moieties |
AU769703B2 (en) * | 1999-04-23 | 2004-01-29 | Kaneka Corporation | Processing aid for thermoplastic resin and thermoplastic resin composition containing the same |
GB2351986B (en) | 1999-07-13 | 2002-12-24 | Sofitech Nv | Latex additive for water-based drilling fluids |
AUPQ164299A0 (en) | 1999-07-14 | 1999-08-05 | Orica Australia Pty Ltd | Aqueous polymer dispersion |
JP4702995B2 (en) | 1999-11-29 | 2011-06-15 | 日本電産サーボ株式会社 | Annular coil polyphase rotating electrical machine and method of use |
US6573325B1 (en) | 2000-04-28 | 2003-06-03 | David York | Aqueous surface treatment compositions |
DE10037629A1 (en) * | 2000-08-02 | 2002-02-14 | Skw Bauwerkstoffe Deutschland | Water-soluble or water-swellable sulfo-containing associative thickening copolymers, process for their preparation and their use |
US6749721B2 (en) * | 2000-12-22 | 2004-06-15 | Kimberly-Clark Worldwide, Inc. | Process for incorporating poorly substantive paper modifying agents into a paper sheet via wet end addition |
ES2196944B1 (en) * | 2001-03-08 | 2005-05-01 | Imrepol , S.L. | MODIFIED ASPHALT FORMULATION FOR WATERPROOFING AND / OR INSONORIZATION OF SURFACES. |
GB2378716B (en) * | 2001-08-08 | 2004-01-14 | Mi Llc | Process fluid |
US7153496B2 (en) * | 2002-01-18 | 2006-12-26 | Noveon Ip Holdings Corp. | Hair setting compositions, polymers and methods |
US7288616B2 (en) * | 2002-01-18 | 2007-10-30 | Lubrizol Advanced Materials, Inc. | Multi-purpose polymers, methods and compositions |
US6926745B2 (en) * | 2002-05-17 | 2005-08-09 | The Clorox Company | Hydroscopic polymer gel films for easier cleaning |
US6916402B2 (en) * | 2002-12-23 | 2005-07-12 | Kimberly-Clark Worldwide, Inc. | Process for bonding chemical additives on to substrates containing cellulosic materials and products thereof |
CA2531687C (en) * | 2003-07-18 | 2011-06-28 | Yi Yan Yang | Thermosensitive polymers for therapeutic use and methods of preparation |
US7402627B2 (en) * | 2003-08-18 | 2008-07-22 | Columbia Insurance Company | Precursor colorant composition for latex paint |
US8329807B2 (en) * | 2003-08-18 | 2012-12-11 | Columbia Insurance Company | Latex paint film resistant to adverse effects of water, and compositions and methods for making same |
US9139676B2 (en) | 2003-08-18 | 2015-09-22 | Benjamin Moore & Co. | Environmentally friendly colorant compositions and latex paints/coatings |
US7892525B2 (en) * | 2003-08-22 | 2011-02-22 | Lubrizol Advanced Materials, Inc. | Antiperspirant gel compositions |
US7205352B2 (en) * | 2003-12-17 | 2007-04-17 | Ethox Chemicals, Llc | Dispersions containing fatty acid esters of styrenated phenol alkoxylates |
US7271211B2 (en) * | 2003-12-17 | 2007-09-18 | Ethox Chemicals, Llc | Dispersions containing fatty acid esters of styrenated phenol alkoxylates |
US7607483B2 (en) * | 2004-04-19 | 2009-10-27 | Halliburton Energy Services, Inc. | Sealant compositions comprising colloidally stabilized latex and methods of using the same |
US7501470B2 (en) * | 2004-12-03 | 2009-03-10 | Rhodia Inc. | Use of polyoxypropylene and polyoxyethylene terpene compounds in emulsion polymerization |
US7488705B2 (en) * | 2004-12-08 | 2009-02-10 | Halliburton Energy Services, Inc. | Oilwell sealant compositions comprising alkali swellable latex |
US20070111900A1 (en) * | 2005-11-11 | 2007-05-17 | Reddy B R | Sealant compositions comprising solid latex |
US20070111901A1 (en) * | 2005-11-11 | 2007-05-17 | Reddy B R | Method of servicing a wellbore with a sealant composition comprising solid latex |
US7670459B2 (en) * | 2004-12-29 | 2010-03-02 | Kimberly-Clark Worldwide, Inc. | Soft and durable tissue products containing a softening agent |
EP1858989B1 (en) | 2005-01-07 | 2015-12-09 | Rhodia Chimie | Aqueous paint compositions comprising a colloidal dispersion of cerium |
ES2389776T3 (en) | 2005-05-31 | 2012-10-31 | Rhodia, Inc. | Compositions that have HASE rheological modifiers |
WO2007101048A2 (en) * | 2006-02-24 | 2007-09-07 | Lubrizol Advanced Materials, Inc. | Polymerizable silicone copolyol macromers and polymers made therefrom |
BRPI0708169B1 (en) * | 2006-02-24 | 2015-08-04 | Lubrizol Advanced Mat Inc | Composition |
GB2446400B (en) * | 2007-02-08 | 2009-05-06 | Mi Llc | Water-based drilling fluid |
FR2912309B1 (en) | 2007-02-13 | 2010-06-04 | Oreal | (EN) METHOD FOR PERMANENTLY DEFORMING KERATIN FIBERS COMPRISING AN APPLICATION STEP OF AN OXIDIZING COMPOSITION CONTAINING A CATIONIC THERAPY POLYMER. |
US9428652B2 (en) * | 2007-06-01 | 2016-08-30 | The Sherwin-Williams Company | Color changing aqueous coatings |
FR2920978B1 (en) | 2007-09-14 | 2012-04-27 | Oreal | COSMETIC COMPOSITION COMPRISING CATIONIC COPOLYMER AND STARCH AND METHOD OF COSMETIC TREATMENT. |
FR2920970B1 (en) | 2007-09-14 | 2010-02-26 | Oreal | COSMETIC COMPOSITIONS CONTAINING CATIONIC COPOLYMER, CYCLODEXTRIN AND SURFACTANT AND USES THEREOF. |
FR2920972B1 (en) | 2007-09-14 | 2009-12-04 | Oreal | COSMETIC COMPOSITION COMPRISING A PARTICULAR CATIONIC POLYMER AND AT LEAST ONE C8-C24 FATTY ACID ESTER AND SORBITAN OXYETHYLENE COMPRISING 2 TO 10 OXYETHYLENE MOTIFS, AND COSMETIC TREATMENT METHOD. |
FR2920969B1 (en) | 2007-09-14 | 2009-12-18 | Oreal | COSMETIC COMPOSITIONS CONTAINING CATIONIC COPOLYMER, AMINO SILICONE AND CATIONIC POLYMER AND USES THEREOF. |
FR2920986B1 (en) | 2007-09-14 | 2010-01-15 | Oreal | COSMETIC COMPOSITIONS CONTAINING CATIONIC COPOLYMER AND PARTICULATE AMINO SILICONE AND USES THEREOF |
FR2920977B1 (en) | 2007-09-14 | 2012-07-27 | Oreal | COSMETIC COMPOSITIONS CONTAINING A CATIONIC COPOLYMER AND A PARTICULAR TRIGLYCERIDE AND USES THEREOF. |
FR2920976B1 (en) | 2007-09-14 | 2009-12-04 | Oreal | COSMETIC COMPOSITION COMPRISING A CATIONIC COPOLYMER AND ANIONIC ASSOCIATIVE POLYMER AND COSMETIC PROCESSING METHOD. |
FR2920971B1 (en) | 2007-09-14 | 2014-03-28 | Oreal | COSMETIC COMPOSITION COMPRISING AT LEAST ONE PARTICULAR CATIONIC POLYMER, AT LEAST ONE SURFACE ACTIVE AGENT, AT LEAST ONE CATIONIC OR AMPHOTERIC POLYMER AND AT LEAST ONE MINERAL PARTICLE, AND METHOD OF COSMETIC TREATMENT. |
JP2009076638A (en) * | 2007-09-20 | 2009-04-09 | Toshiba Corp | Manufacturing method of semiconductor device |
US9388323B2 (en) * | 2008-01-18 | 2016-07-12 | Rhodia Operations | Latex binders, aqueous coatings and paints having freeze-thaw ability and methods for using same |
US7906577B2 (en) * | 2008-01-18 | 2011-03-15 | Rhodia Operations | Latex binders, aqueous coatings and paints having freeze-thaw stability and methods for using same |
US20150133604A1 (en) * | 2008-01-18 | 2015-05-14 | Rhodia Operations | Latex binders, aqueous coatings and paints having freeze-thaw stability and methods for using same |
FR2930440B1 (en) | 2008-04-28 | 2012-12-14 | Oreal | COSMETIC COMPOSITION COMPRISING A CATIONIC POLYURETHANE AND A PARTICULAR POLYACRYLATE AND USES THEREFOR |
CN102439054B (en) | 2009-05-20 | 2014-05-21 | 巴斯夫欧洲公司 | Hydrophobically associating copolymers |
US8362180B2 (en) | 2009-05-20 | 2013-01-29 | Basf Se | Hydrophobically associating copolymers |
EP2287216A1 (en) * | 2009-08-06 | 2011-02-23 | Basf Se | Water soluble associative polymers |
WO2011068820A1 (en) | 2009-12-01 | 2011-06-09 | Lubrizol Advanced Materials, Inc. | Hydrolytically stable multi-purpose polymers |
WO2011068837A2 (en) | 2009-12-01 | 2011-06-09 | Lubrizol Advanced Materials, Inc. | Hydrolytically stable multi-purpose polymers |
SG181500A1 (en) * | 2009-12-11 | 2012-07-30 | Rhodia Operations | Methods and systems for improving open time and drying time of latex binders and aqueous coatings |
BR112012019200A2 (en) * | 2010-02-03 | 2017-06-13 | Basf Se | associative thickener, process for preparing an associative thickener, aqueous thickener composition, use of an associative thickener, paper coating sliding agent, and paper or cardboard. |
EP2534184B1 (en) | 2010-02-12 | 2017-09-27 | Rhodia Operations | Rheology modifier polymer |
WO2011100665A2 (en) * | 2010-02-12 | 2011-08-18 | Rhodia Operations | Rheology modifier compositions and methods of use |
KR101874814B1 (en) * | 2010-02-12 | 2018-07-05 | 로디아 오퍼레이션스 | Compositions with freeze thaw stability |
EA201390769A1 (en) | 2010-11-24 | 2013-12-30 | Басф Се | METHOD OF OIL PRODUCTION BY USING HYDROPHOBIC-ASSOCIATED POLYMERS |
US8939206B2 (en) | 2010-11-24 | 2015-01-27 | Basf Se | Process for mineral oil production using hydrophobically associating copolymers |
EP2457973A1 (en) | 2010-11-24 | 2012-05-30 | Basf Se | Use of a water-soluble, hydrophobically associating copolymer as additive in special oil field applications |
US8752624B2 (en) | 2010-11-24 | 2014-06-17 | Basf Se | Aqueous formulations of hydrophobically associating copolymers and surfactants and use thereof for mineral oil production |
MX2013005518A (en) | 2010-11-24 | 2013-07-05 | Basf Se | Method for oil recovery using hydrophobically associating polymers. |
US9051503B2 (en) | 2010-11-24 | 2015-06-09 | Basf Se | Use of hydrophobically associated copolymer as an additive in specific oilfield applications |
CA2818016C (en) | 2010-11-24 | 2019-04-09 | Basf Se | Aqueous formulations of hydrophobically associating copolymers and surfactants and use thereof for mineral oil production |
EP2694618B1 (en) | 2011-04-08 | 2015-01-28 | Basf Se | Process for producing mineral oil from underground formations |
US8763698B2 (en) | 2011-04-08 | 2014-07-01 | Basf Se | Process for producing mineral oil from underground formations |
EP2756052B2 (en) | 2011-09-13 | 2019-11-20 | Lubrizol Advanced Materials, Inc. | Surfactant responsive emulsion polymerized micro-gels |
JP2014534275A (en) | 2011-09-13 | 2014-12-18 | ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド | Surfactant-responsive microgel |
WO2013040178A1 (en) | 2011-09-13 | 2013-03-21 | Lubrizol Advanced Materials, Inc. | Surfactant responsive dispersion polymerized micro-gels |
CN103917608B (en) * | 2011-11-10 | 2017-11-17 | 巴斯夫欧洲公司 | Paper Coating slurry additives comprising acid monomers, associative monomer and non-ionic monomer |
GB2496675A (en) | 2011-11-18 | 2013-05-22 | Scott Bader Co | Emulsion copolymer latex |
US9271921B2 (en) | 2011-12-14 | 2016-03-01 | Avon Products, Inc. | Cosmetic compositions having persistent tightening effects |
US8771656B2 (en) | 2011-12-14 | 2014-07-08 | Avon Products, Inc | Long-lasting easy wash-off cosmetic compositions |
US9777094B2 (en) | 2012-12-17 | 2017-10-03 | Basf Se | Water-soluble, hydrophobically associating copolymers having novel hydrophobically associating monomers |
EP2931786B1 (en) | 2012-12-17 | 2021-05-05 | Basf Se | Process for preparing a macromonomer |
JP6438411B2 (en) | 2012-12-20 | 2018-12-12 | ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド | Stimulus mitigating polymers and uses |
JP6407885B2 (en) | 2012-12-20 | 2018-10-17 | ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド | Stimulus mitigating polymers and uses |
CN105121480B (en) | 2012-12-21 | 2018-01-09 | 罗地亚经营管理公司 | Composition with the pH response polymers containing MAEP and/or MAHP and use its method |
CN105263974A (en) | 2012-12-21 | 2016-01-20 | 罗地亚经营管理公司 | Anti-settling and thickening compositions and methods for using same |
BR112015019598B1 (en) | 2013-02-19 | 2020-06-23 | Johnson & Johnson Consumer Inc. | METHODS TO IMPROVE THE APPEARANCE OF AND / OR SUBSTANTIALLY REDUCE THE FORMATION OF SCARS AND OTHER VISIBLE EFFECTS OF HEALED WOUNDS, KELOIDS AND HYPERTHROPHIC SCARS |
WO2014138327A1 (en) | 2013-03-08 | 2014-09-12 | Lubrizol Advanced Materials, Inc. | Improved foaming performance in cleansing compositions through the use of nonionic, amphiphilic polymers |
BR112015021530A2 (en) | 2013-03-08 | 2017-07-18 | Lubrizol Advanced Mat Inc | personal care composition and method for mitigating the loss of deposited silicone |
MX2016002325A (en) | 2013-08-22 | 2016-11-30 | Basf Se | Stabilised compositions containing acrylamide polymers, and method for the tertiary production of crude oil using said compositions. |
JP6549583B2 (en) | 2013-12-17 | 2019-07-24 | ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド | Surfactant-responsive emulsion polymerization microgel |
KR20160096204A (en) | 2013-12-23 | 2016-08-12 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | Suspension and stability agent for antidandruff hair care compositions |
US9650323B2 (en) | 2014-03-18 | 2017-05-16 | Rhodia Operations | Tri-substituted aromatic-containing additives and surfactants and methods for use |
EP2955165A1 (en) | 2014-06-12 | 2015-12-16 | Basf Se | Inorganic binding agent composition comprising a copolymer |
US11207248B2 (en) | 2014-11-10 | 2021-12-28 | The Procter And Gamble Company | Personal care compositions with two benefit phases |
US10966916B2 (en) | 2014-11-10 | 2021-04-06 | The Procter And Gamble Company | Personal care compositions |
CN107106474B (en) | 2014-11-10 | 2021-06-01 | 宝洁公司 | Personal care composition with two benefit phases |
WO2016079213A1 (en) * | 2014-11-20 | 2016-05-26 | Basf Se | Rheology modifier for inorganic suspensions |
WO2016083318A1 (en) | 2014-11-24 | 2016-06-02 | Akzo Nobel Chemicals International B.V. | Internal polymeric breaker for viscoelastic surfactant-based fluids |
US20170367963A1 (en) | 2014-12-18 | 2017-12-28 | Lubrizol Advanced Materials, Inc. | Amphiphilic suspension and stability agent for antidandruff hair care compositions |
CN107108454A (en) * | 2014-12-22 | 2017-08-29 | 罗地亚经营管理公司 | The compound of alkoxylate be used for reduce base material coat particle combination purposes and its method |
JP2018502196A (en) | 2014-12-23 | 2018-01-25 | ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド | Laundry detergent composition stabilized with an amphiphilic crosslinker and an amphiphilic rheology modifier crosslinked |
CN104892924B (en) * | 2015-05-21 | 2017-08-25 | 青岛科技大学 | Tristyrylphenol polyoxyethylene ether(Methyl)The preparation method of acrylate |
EP3098381A1 (en) | 2015-05-28 | 2016-11-30 | Basf Se | Formulation comprising at least one hydrophobically associating copolymer, a crosslinking agent and a proppant |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4138381A (en) * | 1975-04-14 | 1979-02-06 | E. I. Du Pont De Nemours And Company | Polymeric thickeners, processes for their preparation and uses thereof |
US4384096A (en) * | 1979-08-27 | 1983-05-17 | The Dow Chemical Company | Liquid emulsion polymers useful as pH responsive thickeners for aqueous systems |
US4421902A (en) * | 1982-09-30 | 1983-12-20 | Rohm And Haas Company | Alkyl, poly(oxyethylene) poly(carbonyloxyethylene) acrylate emulsion copolymers for thickening purposes |
US5082591A (en) * | 1988-05-27 | 1992-01-21 | Rhone-Poulenc Chimie | Surface active agent based on polyoxyalkylenated (1-phenyl ethyl) phenols, the process for preparation thereof and the use thereof for producing emulsifiable concentrated solutions of active materials |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3657175A (en) * | 1969-06-26 | 1972-04-18 | Standard Brands Chem Ind Inc | Carboxylic acid latices providing unique thickening and dispersing agents |
US3652497A (en) * | 1970-04-20 | 1972-03-28 | Gen Latex And Chemical Corp | Polymeric thickeners and method of preparing same |
US3891591A (en) * | 1973-08-13 | 1975-06-24 | Du Pont | Coating compositions |
US4075411A (en) * | 1975-05-23 | 1978-02-21 | Haven Industries, Inc. | Vinyl-polymerizable surfactive monomers |
US4155892A (en) * | 1975-10-03 | 1979-05-22 | Rohm And Haas Company | Polyurethane thickeners for aqueous compositions |
US4079028A (en) * | 1975-10-03 | 1978-03-14 | Rohm And Haas Company | Polyurethane thickeners in latex compositions |
DE2758122A1 (en) * | 1977-12-24 | 1979-07-05 | Basf Ag | WATER-SOLUBLE COPOLYMERISATES BASED ON HYDROPHILIC AETHYLENICALLY UNSATURATED MONOMERS |
CA1188043A (en) * | 1978-12-29 | 1985-05-28 | Ching-Jen Chang | Methacrylic acid emulsion copolymers for thickening purposes |
US4268641A (en) * | 1979-04-24 | 1981-05-19 | Union Carbide Corporation | Acrylic acid-acrylate copolymer thickening agents |
GR78909B (en) * | 1982-08-13 | 1984-10-02 | Sipcam Spa | |
US4469611A (en) * | 1982-11-01 | 1984-09-04 | The Dow Chemical Company | Water-based hydraulic fluids |
US4921902A (en) * | 1984-02-02 | 1990-05-01 | The Dow Chemical Company | Hydrophobie associative composition containing a polymer of a water-soluble monomer and an amphiphilic monomer |
DE3404537A1 (en) * | 1984-02-09 | 1985-08-14 | Hoechst Ag, 6230 Frankfurt | AQUEOUS FUNCTIONAL LIQUIDS BASED ON POLYMERS |
GB8406783D0 (en) * | 1984-03-15 | 1984-04-18 | Allied Colloids Ltd | Prepasted wall-coverings |
CA1285685C (en) * | 1985-02-04 | 1991-07-02 | Ching-Jen Chang | Method for preparation of hydrophobe containing alkali soluble or swellable emulsion copolymers |
EP0214760B1 (en) * | 1985-08-12 | 1990-06-13 | Ciba Specialty Chemicals Water Treatments Limited | Aqueous adhesives and their use |
DE3777441D1 (en) * | 1986-05-07 | 1992-04-23 | Dai Ichi Kogyo Seiyaku Co Ltd | A POLYMERIZABLE PART CONTAINING SURFACE ACTIVE CONNECTIONS. |
FR2601259B1 (en) * | 1986-07-11 | 1990-06-22 | Rhone Poulenc Chimie | NOVEL SURFACTANT COMPOSITIONS BASED ON PHOSPHORIC ESTERS, THEIR PREPARATION PROCESS AND THEIR APPLICATION TO THE FORMULATION OF ACTIVE MATERIALS. |
JPH0212718A (en) * | 1988-06-30 | 1990-01-17 | Omron Tateisi Electron Co | Push-button switch |
FR2633930B1 (en) * | 1988-07-07 | 1991-04-19 | Coatex Sa | THICKENING AGENT FOR MODIFYING THE RHEOLOGICAL CHARACTERISTICS OF AQUEOUS LOADED AND / OR PIGMENTED, WHITE OR COLORED COMPOSITIONS |
DE3925220C1 (en) * | 1989-07-29 | 1991-01-03 | Th. Goldschmidt Ag, 4300 Essen, De | |
US5192592A (en) * | 1990-07-30 | 1993-03-09 | Union Carbide Chemicals & Plastics Technology Corporation | Method of coating substrates utilizing an alkali-functional associative thickner containing coating composition |
JPH0558950A (en) * | 1991-06-21 | 1993-03-09 | Nippon Kayaku Co Ltd | (meth)acrylic acid ester |
FR2693203B1 (en) * | 1992-07-01 | 1994-08-26 | Coatex Sas | Partially or completely water-soluble acrylic copolymer, crosslinked or not and its use. |
CA2157691C (en) † | 1994-09-29 | 1998-08-18 | Joseph Doolan | High performance alkali-swellable rheological additives for aqueous systems |
-
1995
- 1995-06-07 US US08/487,755 patent/US5874495A/en not_active Expired - Lifetime
- 1995-09-29 WO PCT/US1995/012601 patent/WO1996010602A1/en active Search and Examination
- 1995-09-29 ZA ZA9508224A patent/ZA958224B/en unknown
- 1995-09-29 JP JP51209196A patent/JP4290761B2/en not_active Expired - Lifetime
- 1995-09-29 CA CA002200759A patent/CA2200759C/en not_active Expired - Lifetime
- 1995-10-02 EP EP95402199A patent/EP0705854B2/en not_active Expired - Lifetime
- 1995-10-02 ES ES95402199T patent/ES2118514T3/en not_active Expired - Lifetime
- 1995-10-02 DE DE69502067T patent/DE69502067T3/en not_active Expired - Lifetime
- 1995-10-02 NO NO953911A patent/NO953911L/en unknown
- 1995-10-02 FI FI954670A patent/FI954670A/en unknown
- 1995-10-02 DK DK95402199T patent/DK0705854T3/en active
- 1995-10-02 AT AT95402199T patent/ATE165104T1/en not_active IP Right Cessation
-
1996
- 1996-04-02 US US08/627,958 patent/US5770760A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4138381A (en) * | 1975-04-14 | 1979-02-06 | E. I. Du Pont De Nemours And Company | Polymeric thickeners, processes for their preparation and uses thereof |
US4384096A (en) * | 1979-08-27 | 1983-05-17 | The Dow Chemical Company | Liquid emulsion polymers useful as pH responsive thickeners for aqueous systems |
US4421902A (en) * | 1982-09-30 | 1983-12-20 | Rohm And Haas Company | Alkyl, poly(oxyethylene) poly(carbonyloxyethylene) acrylate emulsion copolymers for thickening purposes |
US5082591A (en) * | 1988-05-27 | 1992-01-21 | Rhone-Poulenc Chimie | Surface active agent based on polyoxyalkylenated (1-phenyl ethyl) phenols, the process for preparation thereof and the use thereof for producing emulsifiable concentrated solutions of active materials |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11104479A (en) * | 1997-07-18 | 1999-04-20 | Coatex Sa | Use of surface active structural copolymer as dispersant and/or grinding assistant |
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EP0705854B1 (en) | 1998-04-15 |
DE69502067T2 (en) | 1999-02-04 |
ZA958224B (en) | 1997-02-06 |
DE69502067D1 (en) | 1998-05-20 |
CA2200759C (en) | 2008-04-22 |
ATE165104T1 (en) | 1998-05-15 |
NO953911D0 (en) | 1995-10-02 |
DK0705854T3 (en) | 1998-11-09 |
EP0705854B2 (en) | 2011-09-28 |
US5770760A (en) | 1998-06-23 |
CA2200759A1 (en) | 1996-04-11 |
JPH10509467A (en) | 1998-09-14 |
NO953911L (en) | 1996-04-09 |
JP4290761B2 (en) | 2009-07-08 |
DE69502067T3 (en) | 2012-05-31 |
FI954670A (en) | 1996-04-04 |
ES2118514T3 (en) | 1998-09-16 |
FI954670A0 (en) | 1995-10-02 |
EP0705854A1 (en) | 1996-04-10 |
US5874495A (en) | 1999-02-23 |
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