WO1997009400A1 - Utilisation en tant qu'agents thermoepaississants de copolymeres multiblocs - Google Patents
Utilisation en tant qu'agents thermoepaississants de copolymeres multiblocs Download PDFInfo
- Publication number
- WO1997009400A1 WO1997009400A1 PCT/FR1996/001373 FR9601373W WO9709400A1 WO 1997009400 A1 WO1997009400 A1 WO 1997009400A1 FR 9601373 W FR9601373 W FR 9601373W WO 9709400 A1 WO9709400 A1 WO 9709400A1
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- use according
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/04—Aqueous well-drilling compositions
- C09K8/06—Clay-free compositions
- C09K8/12—Clay-free compositions containing synthetic organic macromolecular compounds or their precursors
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/43—Thickening agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/04—Aqueous well-drilling compositions
- C09K8/14—Clay-containing compositions
- C09K8/18—Clay-containing compositions characterised by the organic compounds
- C09K8/22—Synthetic organic compounds
- C09K8/24—Polymers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M119/00—Lubricating compositions characterised by the thickener being a macromolecular compound
- C10M119/24—Lubricating compositions characterised by the thickener being a macromolecular compound containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M119/00—Lubricating compositions characterised by the thickener being a macromolecular compound
- C10M119/26—Lubricating compositions characterised by the thickener being a macromolecular compound containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/04—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/04—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2221/041—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds involving sulfurisation of macromolecular compounds, e.g. polyolefins
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/04—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2221/043—Polyoxyalkylene ethers with a thioether group
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/06—Instruments or other precision apparatus, e.g. damping fluids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
Definitions
- the present invention relates to polymers having heat-thickening properties in an aqueous medium.
- heat-thickening polymers is understood to mean polymers whose viscosity in an aqueous medium remains constant or increases over a wide temperature range, unlike conventional polymers whose viscosity decreases very significantly with the rise in temperature. It has been described in EP-A-583 814 of polymers having thermo-thickening properties, said polymers being in the form of copolymers consisting of a perfectly water-soluble chain on which other segments exhibiting a water-soluble transition at a critical temperature called LCST (low critical soluble temperature) are grafted.
- LCST critical critical soluble temperature
- thermo thickening the segments which have become hydrophobic tend to associate, which leads to the formation of a network of high molecular mass and therefore to an increase in viscosity or at least to a non-decrease in viscosity creating the property. thermo thickening.
- the critical temperature of the exemplified segments of the prior art can be high, it is for example greater than 100 ° C. for polyoxyethylene.
- the thermo-thickening effect only appears at temperatures for which this effect is not always sought.
- certain thermo-thickening polymers cannot be used in applications carried out at low temperature.
- thermo-thickening polymers in the presence of a salt which makes it possible to develop the thermo-thickening effect at lower temperature.
- a salt is not possible in the context of certain applications such as phytosanitary applications or those of the paper industry. It is therefore an object of the invention to provide polymers having thermo-thickening properties at a temperature below the critical LCST temperature of the links.
- Another object of the invention is to provide a means of controlling the temperature at which the heat-thickening effect of a copolymer appears, the nature of the water-soluble chain and of the links being given.
- the invention relates to the use as heat-thickening agents of linear multiblock copolymers of general formula (I) or (II): - [E - Y - C - S - A - S - C - Y f- Struktur(I)
- E represents a polyoxyalkylene block, each alkylene link having at most 6 carbon atoms
- - A represents a water-soluble polymer block derived from at least one monomer chosen from ethylenic monomers, - X is a chalcogene,
- - Y is an oxygen atom or a group -N-R ', R "being:
- a linear or branched alkyl group optionally comprising at least one heteroatom and optionally a tertiary amine group, or. a C 3 -C 8 cycloalkyie radical, or. an aryl, aralkyl or alkylaryl group,
- R is a linear or branched alkyl, aralkyl or alkylaryl group
- the copolymers according to the invention are linear and do not have lateral segments grafted onto the main chain of type A. They have an alternation of polyoxyalkylene polymer blocks E and of water-soluble polymer blocks A derived from ethylene type monomers, linked together by a ball joint:
- the polyoxyalkylenated blocks E have a critical temperature (LCST), while the polymer blocks A are water-soluble in any temperature range.
- the copolymers used must have a molecular mass greater than 250,000 g / mol, said molecular mass being measured by gel chromatography (G PC) in aqueous phase in polyoxyethylene equivalents.
- multiblock polymers are used whose polyoxyalkylenated blocks E comprise a number of units i of at least 25, preferably at most 1000, even more preferably between 200 and 400.
- multiblock polymers are used whose content by weight T of polyoxyalkylenated blocks E is at least 3%, preferably at most 50%, even more preferably between 5 and 20%.
- R being able to be a methyl or ethyl group.
- the polyoxyalkylenated blocks E are polyethylene oxide blocks.
- the water-soluble polymer blocks A can result from the polymerization of water-soluble ethylene monomers and in particular vinyl or diene monomers. They may, for example, be the following water-soluble ethylene monomers:
- acrylic and methacrylic monomers chosen more particularly from: acrylic or methacrylic acid, - acrylamides and their derivatives such as (meth) acrylamides, N (monoalkyl) acrylamide or N (dialkyl) acrylamides,
- sulfonated monomers chosen from sulfo-acetyl (meth) acrylates, acid 2, acrylamide-methyl-propane sulfonic (AMPS) and its alkalis, vinylsulfonate, methallylsulfonate.
- sulfo-acetyl (meth) acrylates acid 2, acrylamide-methyl-propane sulfonic (AMPS) and its alkalis, vinylsulfonate, methallylsulfonate.
- AMPS acrylamide-methyl-propane sulfonic
- the A sequences result from the polymerization of acrylic acid, AMPS or acrylamide.
- the water-soluble blocks A can advantageously result from the polymerization of water-soluble ethylene monomers and from a small amount of organosoluble ethylene monomers. This small amount of organosoluble monomers makes it possible to control the solubility of the hydrophilic sequences A in water. The relative amounts of these two types of monomers in the A sequences are adjusted according to the knowledge of a person skilled in the art.
- organosoluble ethylenic monomers can be chosen from:
- - styrene monomers such as styrene, ⁇ -methylstyrene, tert-butylstyrene and vinyltoluene, - vinyl esters, butadiene, chloroprene, isoprene, ...
- multiblock copolymers are used in which X is a sulfur atom and Y is an oxygen atom.
- multiblock polymers are obtained whose sequences are linked together by xanthate disulphide ball joints:
- the content of heat-thickening copolymer in the medium to be thickened is at most 15% by weight, preferably at least 0.5%.
- the block copolymers according to the invention can be used in applications in which it is desired to maintain a viscosity level over a wide temperature and application range in the presence of salt or not.
- copolymers described above in the paper industry, in the paint industry, in industrial cleaning fluids, in hydraulic fluids and in particular in water-based lubricants or in drilling and cementing of oil wells.
- Said fluids can in particular be used in the paper industry in paper coating baths, in particular for aqueous paper coating formulations or in industrial paints for drying paints by heating.
- the polymers used according to the invention have the advantage of having a heat-thickening effect at a temperature below the critical temperature of their polyoxyalkylenated blocks without the need to add a salt. This effect can possibly be exacerbated by the use of the copolymers in basic medium, by adding for example a base such as sodium hydroxide.
- Example 1 PAA / POE multi-block copolymer with a molecular mass of 270,000 ⁇ / mol
- Polyoxyethylene xanthate disulfide (POEX) fertilizers with a molecular weight of 10,000 g / mol are prepared according to the teaching of application EP-A-0539256.
- the polyacrylic acid / polyoxyethylene (PAA / POE) copolymer obtained contains 12% by weight of POE with a mass of 10,000 g / mol, therefore the number of units i of which is 227. Its molecular mass is measured in polyoxyethylene equivalents by GPC in the aqueous phase: it is 270,000 g / mol.
- This multiblock copolymer incorporating xanthate disulfide groups has the following formula:
- - A is a polymer block derived from the acrylic acid monomer.
- this copolymer exhibits a heat-thickening effect from 70 ° C. without adding salt, whereas the polyoxyethylene (POE) blocks have an LCST greater than 100 ° C.
- Example 2 PAA / POE multi-block copolymer with a molecular mass of 400,000 o / mol
- POE with a molecular mass of 10,000 g / mol, ie a number of units i of 227, is obtained according to the procedure described in Example 1, but with 0.4 g of ammonium persulfate. Its molecular weight in polyoxyethylene equivalents is measured by
- GPC it is 400,000 g / mol.
- the pH is brought to 4 with sodium hydroxide and the viscosity is measured as a function of the temperature using a rheometer of the CARRI-MED type.
- Comparative example 3 PAA / POE multi-block copolymer with a molecular mass of 200,000 g / mol
- this multiblock copolymer exhibits a heat-thickening effect at a temperature below 100 ° C. only in the presence of salt.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Paper (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU69348/96A AU6934896A (en) | 1995-09-08 | 1996-09-06 | Use of multi-block copolymers as thermo-thickeners |
EP96930227A EP0865477A1 (fr) | 1995-09-08 | 1996-09-06 | Utilisation en tant qu'agents thermoepaississants de copolymeres multiblocs |
US09/029,702 US6124382A (en) | 1995-09-08 | 1996-09-06 | Use of multi-block copolymers as thermo-thickeners |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9510517A FR2738573B1 (fr) | 1995-09-08 | 1995-09-08 | Utilisation en tant qu'agents thermoepaississants de copolymeres multiblocs |
FR95/10517 | 1995-09-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997009400A1 true WO1997009400A1 (fr) | 1997-03-13 |
Family
ID=9482367
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR1996/001373 WO1997009400A1 (fr) | 1995-09-08 | 1996-09-06 | Utilisation en tant qu'agents thermoepaississants de copolymeres multiblocs |
Country Status (5)
Country | Link |
---|---|
US (1) | US6124382A (fr) |
EP (1) | EP0865477A1 (fr) |
AU (1) | AU6934896A (fr) |
FR (1) | FR2738573B1 (fr) |
WO (1) | WO1997009400A1 (fr) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2773161A1 (fr) * | 1997-12-31 | 1999-07-02 | Rhodia Chimie Sa | Procede de synthese de polymeres a blocs |
FR2780422A1 (fr) * | 1998-06-26 | 1999-12-31 | Rhodia Chimie Sa | Composition thermoepaississante pour bains de couchage a base d'un copolymere possedant une temperature critique inferieure de solubilite |
FR2788008A1 (fr) * | 1998-12-30 | 2000-07-07 | Inst Curie | Milieu thermosensible pour la separation electrocinetique d'especes au sein d'un canal de separation |
WO2002000746A2 (fr) * | 2000-06-30 | 2002-01-03 | Institut Curie | Solution de traitement de surface minimisant les phenomenes d'adsorption et/ou d'electroosmose |
WO2002032560A2 (fr) * | 2000-10-20 | 2002-04-25 | Rhodia Chimie | Procede de preparation d'une emulsion dont la phase organique est de forte viscosite |
US8975328B2 (en) | 2000-06-30 | 2015-03-10 | Institute Curie | Non-thermosensitive medium for analyzing species in a channel and for minimizing adsorption and/or electroosomosic phenomena |
US9658189B2 (en) | 2000-06-30 | 2017-05-23 | Institute Curie | Non-thermosensitive medium for analyzing species in a channel and for minimizing adsorption and/or electroosomosic phenomena |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040044130A1 (en) * | 1998-06-26 | 2004-03-04 | Labeau Marie-Pierre | Heat thickening composition for coating slips based on a copolymer having a lower critical solubility temperature |
FR2802208B1 (fr) * | 1999-12-09 | 2003-02-14 | Rhodia Chimie Sa | Procede de synthese de polymeres par polymerisation radicalaire controlee a l'aide de xanthates |
DE60218864T2 (de) * | 2001-05-04 | 2007-11-22 | Rhodia Inc. | Verfahren zur herstellung von latices durch verwendung von block copolymere als tensid |
WO2002090409A2 (fr) * | 2001-05-04 | 2002-11-14 | Rhodia Chimie | Copolymeres a blocs tensioactifs prepares par polymerisation radicalaire controlee |
WO2012142235A1 (fr) * | 2011-04-15 | 2012-10-18 | Corsicana Technologies, Inc. | Hydrogels thermosensibles et solutions polymères thermosensibles |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0539256A1 (fr) * | 1991-10-23 | 1993-04-28 | Rhone-Poulenc Chimie | Polymères à groupements disulfure de xanthate et leur procédé de préparation |
EP0583814A1 (fr) * | 1992-08-20 | 1994-02-23 | Sofitech N.V. | Polymères thermoviscosifiants, leur synthèse et leurs applications notamment dans l'industrie pétrolière |
EP0629649A1 (fr) * | 1993-06-16 | 1994-12-21 | Sofitech N.V. | Polymères rhéofluidifiants, leur synthèse et leurs applications notamment dans l'industrie pétrolière |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2651781B1 (fr) * | 1989-09-14 | 1991-12-06 | Norsolor Sa | Polymeres a groupements disulfure de thiurame et leur preparation. |
-
1995
- 1995-09-08 FR FR9510517A patent/FR2738573B1/fr not_active Expired - Fee Related
-
1996
- 1996-09-06 WO PCT/FR1996/001373 patent/WO1997009400A1/fr not_active Application Discontinuation
- 1996-09-06 AU AU69348/96A patent/AU6934896A/en not_active Abandoned
- 1996-09-06 US US09/029,702 patent/US6124382A/en not_active Expired - Fee Related
- 1996-09-06 EP EP96930227A patent/EP0865477A1/fr not_active Ceased
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0539256A1 (fr) * | 1991-10-23 | 1993-04-28 | Rhone-Poulenc Chimie | Polymères à groupements disulfure de xanthate et leur procédé de préparation |
EP0583814A1 (fr) * | 1992-08-20 | 1994-02-23 | Sofitech N.V. | Polymères thermoviscosifiants, leur synthèse et leurs applications notamment dans l'industrie pétrolière |
EP0629649A1 (fr) * | 1993-06-16 | 1994-12-21 | Sofitech N.V. | Polymères rhéofluidifiants, leur synthèse et leurs applications notamment dans l'industrie pétrolière |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2773161A1 (fr) * | 1997-12-31 | 1999-07-02 | Rhodia Chimie Sa | Procede de synthese de polymeres a blocs |
FR2780422A1 (fr) * | 1998-06-26 | 1999-12-31 | Rhodia Chimie Sa | Composition thermoepaississante pour bains de couchage a base d'un copolymere possedant une temperature critique inferieure de solubilite |
WO2000000528A1 (fr) * | 1998-06-26 | 2000-01-06 | Rhodia Chimie | Composition thermoepaississante pour bains de couchage a base d'un copolymere possedant une temperature critique inferieure de solubilite |
FR2788008A1 (fr) * | 1998-12-30 | 2000-07-07 | Inst Curie | Milieu thermosensible pour la separation electrocinetique d'especes au sein d'un canal de separation |
WO2000040958A1 (fr) * | 1998-12-30 | 2000-07-13 | Institut Curie | Milieu thermosensible pour la separation d'especes au sein d'un canal de separation |
JP2002534679A (ja) * | 1998-12-30 | 2002-10-15 | アンスティテュ キュリィ | 分離チャネルにおいて種を分離するための感熱性媒体 |
FR2810905A1 (fr) * | 2000-06-30 | 2002-01-04 | Inst Curie | Additif pour minimiser les phenomenes d'adsorption et/ou d'electroosmose |
WO2002000746A2 (fr) * | 2000-06-30 | 2002-01-03 | Institut Curie | Solution de traitement de surface minimisant les phenomenes d'adsorption et/ou d'electroosmose |
WO2002000746A3 (fr) * | 2000-06-30 | 2003-09-04 | Inst Curie | Solution de traitement de surface minimisant les phenomenes d'adsorption et/ou d'electroosmose |
US8975328B2 (en) | 2000-06-30 | 2015-03-10 | Institute Curie | Non-thermosensitive medium for analyzing species in a channel and for minimizing adsorption and/or electroosomosic phenomena |
US9658189B2 (en) | 2000-06-30 | 2017-05-23 | Institute Curie | Non-thermosensitive medium for analyzing species in a channel and for minimizing adsorption and/or electroosomosic phenomena |
WO2002032560A2 (fr) * | 2000-10-20 | 2002-04-25 | Rhodia Chimie | Procede de preparation d'une emulsion dont la phase organique est de forte viscosite |
FR2815637A1 (fr) * | 2000-10-20 | 2002-04-26 | Rhodia Chimie Sa | Procede de preparation d'une emulsion dont la phase huileuse est de forte viscosite |
WO2002032560A3 (fr) * | 2000-10-20 | 2002-06-27 | Rhodia Chimie Sa | Procede de preparation d'une emulsion dont la phase organique est de forte viscosite |
Also Published As
Publication number | Publication date |
---|---|
US6124382A (en) | 2000-09-26 |
AU6934896A (en) | 1997-03-27 |
FR2738573A1 (fr) | 1997-03-14 |
FR2738573B1 (fr) | 1997-10-17 |
EP0865477A1 (fr) | 1998-09-23 |
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