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GB2077750A - Method and Composition for Thickening Aqueous Based Compositions - Google Patents

Method and Composition for Thickening Aqueous Based Compositions Download PDF

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Publication number
GB2077750A
GB2077750A GB8116871A GB8116871A GB2077750A GB 2077750 A GB2077750 A GB 2077750A GB 8116871 A GB8116871 A GB 8116871A GB 8116871 A GB8116871 A GB 8116871A GB 2077750 A GB2077750 A GB 2077750A
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GB
United Kingdom
Prior art keywords
thickener
water
aqueous based
emulsion
based compositions
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB8116871A
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GB2077750B (en
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Scott Bader Co Ltd
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Scott Bader Co Ltd
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Publication date
Application filed by Scott Bader Co Ltd filed Critical Scott Bader Co Ltd
Priority to GB8116871A priority Critical patent/GB2077750B/en
Publication of GB2077750A publication Critical patent/GB2077750A/en
Application granted granted Critical
Publication of GB2077750B publication Critical patent/GB2077750B/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/02Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/03Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/06Solidifying liquids
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/43Thickening agents
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/02Well-drilling compositions
    • C09K8/03Specific additives for general use in well-drilling compositions
    • C09K8/035Organic additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00Characterised by the use of homopolymers or 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 of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/24Homopolymers or copolymers of amides or imides
    • C08J2333/26Homopolymers or copolymers of acrylamide or methacrylamide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/24Homopolymers or copolymers of amides or imides
    • C08L33/26Homopolymers or copolymers of acrylamide or methacrylamide

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Engineering & Computer Science (AREA)
  • Dispersion Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paper (AREA)

Abstract

Aqueous based compositions are thickened by mixing in a thickener which is in the form of a water-in-oil emulsion. Preferably the thickener contains a water soluble acrylamide or methacrylamide homopolymer or a copolymer of (meth)acrylamide with other suitable (e.g. carboxylic acid or cationic) monomers. The polymers may be lightly cross-linked. The thickeners are of low viscosity and easy to handle, but act to thicken aqueous based compositions effectively and quickly, typically dissolving in water in about one minute. They are also resistant to bacterial attack. Examples of aqueous compositions which may be thickened are emulsion paints, carpet backing compounds, textile pigment printing pastes, drilling muds, rubber latex, and wallpaper paste.

Description

SPECIFICATION Method of Thickening Thickeners for aqueous based compositions such as paints, adhesives, textile printing pastes, carpet backings, cosmetics, drilling muds, latices etc are usually natural or synthetic products supplied as solids or dilute solutions. Typical examples of natural or modified natural products are starches, carboxymethyl cellulose, hydroxyethyl cellulose etc. and among the synthetic products used are polyvinyl alcohol, sodium polyacrylate gels etc. These materials are often difficult to handle insofar as they are difficult to dissolve and use, they are not very efficient, they are variable in quality and possess other technical disadvantages like being prone to bacterial attack.
We have now discovered that inverse (i.e. water-in-oil) emulsions of water soluble polyacrylamide and polymethacrylamide homopolymers and copolymers of these with acrylic or methacrylic acids, cationic monomers such as dimethylaminoethyl methacrylate quarternised with dimethyl sulphate etc. can be employed as efficient, easy to use thickener in these systems. The ratios of these monomers can range from 100/1 0 (i.e. (meth) acrylamide homopolymer to 10 (methyl) acrylamide/90 comonomer). Minor amounts of other ethylenically unsaturated monomers may be included. Some of these inverse emulsions of high molecular weight, greater than 1 xl 06, preferably greater than 6x 106, have been used as flocculants.In this new use they overcome the well known problems of dissolving solid products which can take several hours since the polymer has always been in the aqueous phase.
In the present invention we have found that by reversing the emulsion (whether by the addition of water or the addition of a reversing surfactant and water) the low viscosity water in oil emusion is almost instantaneously inverted to an extremely viscous paste of water soluble polymer in the aqueous phase.
Formulations can be provided wherein the water phase of the inverse emulsion includes a reversing surfactant so that addition of pure water will cause reversion to an oil in water-emulsion. But otherwise the addition of a water soluble inversion surfactant to either the inverse emulsion or the water causes the water in oil emulsion to revert and become water soluble and because the emulsion is essentially already in the aqueous phase, rapid solubility occurs. Typically the dissolution in water takes around 1 minute compared to several hours for solid materials.
It is possible to produce lightly crosslinked products of this type by including a small amount, 0.15% by weight, of a di- or poly-functional olefinically unsaturated compound such as allyl methacrylate, diallyl phthalate, divinyl benzene, triallyl isocyanurate or methylene bis-acrylamide in the polymer.
These water-in-oil emulsions are of low viscosity 200-800 cps at 250C (typically 500 cps) and 1 5-40% solids (typically 2530%). They can easily be inverted in water based systems to give very high solution viscosities.
The water-in-oil emulsions typically consist oft 1 5-40% (typically 25%) polymer solids 2-1 0% (typically 5%) oil soluble surfactant HLB below 7 1 3-25% (typically 20%) oil phase usually a hydrocarbon such as white spirit, toluene, Isopar * or a plasticiser such as dibutyl phthalate.
50% water.
*(!)=Esso trade name.
Up to 5 p.p.h. of an inversion surfactant (usually water soluble) may be incorporated.
Sorbitan mono oleate can be used as an oil-soluble surfactant.
The main advantages of using these water in oil emulsions over other solid and liquid products are their ease of production, ease of handling, rapid solubility, efficiency, freedom from bacterial attack, salt stability and temperature stability coupled with low cost.
The following examples illustrate the use of these inverse emulsions as thickeners.
Example 1 Use in thickening emulsion paints.
In this example, Thickener A is a 25% active water in oil emulsion, containing an inversion surfactant, of an acrylamide/sodium acrylate copolymer crosslinked with 0.5% of allyl methacrylate.
The following paint formulation was used:- Water 100 Thickener (solid) 2.2 Dispersant (solid) 1.8 Antifoam 0.9 Pigments 385.0 (Mixture of titanium dioxide and calcium carbonate) Binder latex 298.0 Water 158.0 The binder latex used was a styrene/butyl acrylate emulsion of 55% solids.
The paints were made by dissolving the thickener in water (:D) then adding the pigment dispersant and antifoam. The pigments were then dispersed in this mixture using a high speed stirrer.
Finally the binder latex and water were added. Two paints were made, one using Thickener A, the other using a conventional hydroxyethyl cellulose thickener.
When Thickener A was used the ease of handling, ease of mixing and ease of dissolution were readily apparent. The rheology of the paints were similar and the viscosity of the paint made from Thickener A was slightly higher.
Using Thickener A, unlike the hydroxyethyl cellulose, paints may be made by omitting the thickener from the dispersion stage and post adding this after the binder latex. This method offers process and quality control advantages.
Example 2 Use in thickening carpet backing compounds.
Thickener B was used in this example and this is a 25% active water in oil emulsion, containing inversion surfactant, of acrylamide/sodium acrylate copolymer crosslinked with 0.25% of diallyl phthalate.
Two carpet backing compounds were made. These consisted of thickener styrene/butadiene latex filler, dispersing agent for filling and antifoam. One mixture was made using Thickener B and the other using the same amount (on a solids basis) of a conventional acrylic emulsion thickener.
The use of Thickener B produced a compound having a viscosity 20% higher than the conventional product indicating a iower amount may be used to achieve a given viscosity.
Example 3 Use in thickening textile pigment printing pastes.
In this example Thickener C was used. This is a 25% active water in oil emulsion, containing inversion surfactant, of acrylamide/ammonium acrylate copolymer crosslinked with 0.50% of allyl methacrylate. This product was compared to a well known commerical product based on an ethylene/maleic anhydride polymer in dry powder form.
The Thickener C produced pastes which thicken in one minute compared to the lengthy time for the conventional product. In addition, unlike the conventional product, the addition of ammonia was not necessary.
Printing performacne was similar.
Example 4 Use in thickening Drilling Muds for oil recovery.
In this example, Thickener D was used. This is a 25% active water in oil emulsion of an acrylamide/sodium acrylate copolymer. (No inversion surfactant is necessary in this example).
Two typical sea water based bentonite muds were made up one using Thickener D and the other using an equivalent amount of a conventional solid, high molecular weight carboxymethyl cellulose (CMC). The formulation based on Thickener D showed a higher viscosity, a higher yield point and lower fluid loss in addition to a much shorter dissolving/mixing time.
Example 5 Use in latex thickening.
In this example, Thickener E was used. This is a 25% active water in oil emulsion, containing an inversion surfactant, of an acrylamide/sodium acrylate copolymer crosslinked with 3% divinyl benzene.
Natural rubber latex was thickened using Thickener E and separately an equivalent amount of a conventional sodium polyacrylate gel thickener. The Thickener E was much easier to handle than the gel and exhibited greater thickening efficiency.
Example 6 Use in thickening water for a wallpaper paste.
In this example Thickener F was used. This is a 25% active water in oil emulsion containing an inversion surfactant of an acrylamide/sodium acrylate copolymer crosslinked with 0.1% of allyl methacrylate.
Water was thickened by stirring in 3% of Thickener F and in comparison an equivalent amount of conventional dry starch paste. The materials produced similar viscosities but the Thickener F dissolved in 1 minute compared to 1 5 minutes for the starch. The thickened adhesive showed good open time, grab slip etc. and did not suffer from bacterial attack.

Claims (9)

Claims
1. A method of thickening an aqueous based composition by mixing the composition with a thickener which is a water-in-oil emulsion.
2. A method according to Claim 1 in which the water phase of the emulsion contains water soluble polyacrylamide or polymethacrylamide homopolymers or copolymers of these with each other and/or with acrylic or methacrylic acids, cationic monomers, or any mixtures of these.
3. A method according to Claim 2 in which the said polymers make up 1 5 to 40% of the thickener.
4. A method according to Claim 3 in which the said polymers make up 2530% of the thickener.
5. A method according to any one of Claims 2 to 4 in which the said polymers are lightly crosslinked by incorporation of 0.1 to 5% by weight of a di- or poly-functional olefinically unsaturated compound.
6. A method according to any one of Claims 2 to 5 in which an inversion surfactant is added to the thickener.
7. A thickener for aqueous based compositions which is a water in oil emulsion.
8. A thickener according to Claim 7 in which the water phase of the emulsion contains water soluble polyacrylamide or polymethacrylamide homopolymers or copolymers of these with each other and/or with acrylic or methacrylic acids, cationic monomers, or any mixture of these.
9. An aqueous based compound thickened by the method of any one of Claims 1 to 6.
GB8116871A 1981-06-02 1981-06-02 Method and composition for thickening aqueous based compositions Expired GB2077750B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB8116871A GB2077750B (en) 1981-06-02 1981-06-02 Method and composition for thickening aqueous based compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB8116871A GB2077750B (en) 1981-06-02 1981-06-02 Method and composition for thickening aqueous based compositions

Publications (2)

Publication Number Publication Date
GB2077750A true GB2077750A (en) 1981-12-23
GB2077750B GB2077750B (en) 1985-04-11

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2164373A (en) * 1984-09-12 1986-03-19 Nat Starch Chem Corp Fluid loss control agents for drilling fluids containing divalent cations
US4585820A (en) * 1981-10-09 1986-04-29 Ciba-Geigy Corporation Mixtures of a polyacrylic acid and a copolymer of acrylic acid and acrylamide as thickeners in printing pastes for dyeing and printing fibre material
EP0186361A2 (en) 1984-12-10 1986-07-02 Scott Bader Company Limited Thickeners for thickening aqueous media
US4626363A (en) * 1984-08-29 1986-12-02 National Starch And Chemical Corporation Cationic acrylamide emulsion polymer brine thickeners
US4737541A (en) * 1983-06-23 1988-04-12 The Dow Chemical Company Thickening agents for industrial formulations
GB2247690A (en) * 1990-07-13 1992-03-11 Jan Jozef Korab Line marking paint
EP0649894A1 (en) * 1993-10-26 1995-04-26 Lafarge Nouveaux Materiaux Adhesive compositions based on aqueous dispersions of synthetic resins and their utilisation for glueing of wall or floor coverings
GB2294466A (en) * 1994-10-26 1996-05-01 Polycell Prod Ltd Two-pack adhesive composition
US5688514A (en) * 1991-03-08 1997-11-18 Scott Bader Company Limited Thickeners for products for topical application
US5721313A (en) * 1995-11-02 1998-02-24 Rhone-Poulenc Inc. Crosslinked polymer composition
CN103225216A (en) * 2013-05-13 2013-07-31 江苏兴达文具集团有限公司 Environment-friendly textile pigment and preparation method thereof
CN107922821A (en) * 2015-08-07 2018-04-17 艺康美国股份有限公司 Nonionic transforming agent and application method for Water-In-Oil latex
WO2022182726A1 (en) * 2021-02-23 2022-09-01 Hercules Llc Acrylamide polymer inverse emulsions containing rheology modifiers and architectural coating compositions derived therefrom

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4585820A (en) * 1981-10-09 1986-04-29 Ciba-Geigy Corporation Mixtures of a polyacrylic acid and a copolymer of acrylic acid and acrylamide as thickeners in printing pastes for dyeing and printing fibre material
US4737541A (en) * 1983-06-23 1988-04-12 The Dow Chemical Company Thickening agents for industrial formulations
US4626363A (en) * 1984-08-29 1986-12-02 National Starch And Chemical Corporation Cationic acrylamide emulsion polymer brine thickeners
GB2164373A (en) * 1984-09-12 1986-03-19 Nat Starch Chem Corp Fluid loss control agents for drilling fluids containing divalent cations
US4600515A (en) * 1984-09-12 1986-07-15 National Starch And Chemical Corporation Fluid loss control agents for drilling fluids containing divalent cations
EP0186361A2 (en) 1984-12-10 1986-07-02 Scott Bader Company Limited Thickeners for thickening aqueous media
EP0186361A3 (en) * 1984-12-10 1988-04-20 Scott Bader Company Limited Thickeners for thickening aqueous media
GB2247690A (en) * 1990-07-13 1992-03-11 Jan Jozef Korab Line marking paint
GB2247690B (en) * 1990-07-13 1993-09-01 Jan Jozef Korab Line marking paint
US5804202A (en) * 1991-03-08 1998-09-08 Scott Bader Company Limited Thickeners for products for topical application
US5688514A (en) * 1991-03-08 1997-11-18 Scott Bader Company Limited Thickeners for products for topical application
US5928656A (en) * 1991-03-08 1999-07-27 Scott Bader Company Limited Thickeners for products for topical application
US6051245A (en) * 1991-03-08 2000-04-18 Scott Bader Company Limited Thickeners for products for topical application
WO1995011946A1 (en) * 1993-10-26 1995-05-04 Lafarge Materiaux De Specialites Aqueous dispersion-based adhesive compositions and use thereof
FR2711666A1 (en) * 1993-10-26 1995-05-05 Lafarge Nouveaux Materiaux Adhesive compositions based on aqueous dispersions of synthetic resins and their use for bonding wall or floor coverings.
EP0649894A1 (en) * 1993-10-26 1995-04-26 Lafarge Nouveaux Materiaux Adhesive compositions based on aqueous dispersions of synthetic resins and their utilisation for glueing of wall or floor coverings
GB2294466A (en) * 1994-10-26 1996-05-01 Polycell Prod Ltd Two-pack adhesive composition
US5811485A (en) * 1994-10-26 1998-09-22 Polycell Products Ltd. Two-pack adhesive composition
US5721313A (en) * 1995-11-02 1998-02-24 Rhone-Poulenc Inc. Crosslinked polymer composition
CN103225216A (en) * 2013-05-13 2013-07-31 江苏兴达文具集团有限公司 Environment-friendly textile pigment and preparation method thereof
CN107922821A (en) * 2015-08-07 2018-04-17 艺康美国股份有限公司 Nonionic transforming agent and application method for Water-In-Oil latex
WO2022182726A1 (en) * 2021-02-23 2022-09-01 Hercules Llc Acrylamide polymer inverse emulsions containing rheology modifiers and architectural coating compositions derived therefrom

Also Published As

Publication number Publication date
GB2077750B (en) 1985-04-11

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PE20 Patent expired after termination of 20 years

Effective date: 20010601