WO2022024791A1 - ポリビニルアルコール系重合体 - Google Patents

ポリビニルアルコール系重合体 Download PDF

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Publication number
WO2022024791A1
WO2022024791A1 PCT/JP2021/026688 JP2021026688W WO2022024791A1 WO 2022024791 A1 WO2022024791 A1 WO 2022024791A1 JP 2021026688 W JP2021026688 W JP 2021026688W WO 2022024791 A1 WO2022024791 A1 WO 2022024791A1
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monomer
polyvinyl alcohol
based polymer
vinyl ester
copolymer
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French (fr)
Japanese (ja)
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明宏 山下
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Denka Co Ltd
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Denka Co Ltd
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Priority to ES21850134T priority Critical patent/ES3032513T3/es
Priority to CN202180035703.6A priority patent/CN115698098A/zh
Priority to US17/927,523 priority patent/US12448469B2/en
Priority to EP21850134.4A priority patent/EP4144769B1/en
Priority to JP2022540172A priority patent/JP7561854B2/ja
Publication of WO2022024791A1 publication Critical patent/WO2022024791A1/ja
Anticipated expiration legal-status Critical
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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
    • C08F16/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
    • C08F16/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an alcohol radical
    • C08F16/04—Acyclic compounds
    • C08F16/06—Polyvinyl alcohol ; Vinyl alcohol
    • 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
    • C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
    • C08F216/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an alcohol radical
    • C08F216/04—Acyclic compounds
    • C08F216/06—Polyvinyl alcohol ; Vinyl alcohol
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/24—Macromolecular compounds
    • C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B24/2623—Polyvinylalcohols; Polyvinylacetates
    • 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
    • C08F218/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
    • C08F218/02—Esters of monocarboxylic acids
    • C08F218/04—Vinyl esters
    • C08F218/08—Vinyl acetate
    • 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
    • C08F8/00—Chemical modification by after-treatment
    • C08F8/12—Hydrolysis
    • 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
    • C09K8/03—Specific additives for general use in well-drilling compositions
    • C09K8/035—Organic additives
    • 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
    • C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
    • C09K8/46—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
    • C09K8/467—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
    • 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
    • C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
    • C09K8/46—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
    • C09K8/467—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
    • C09K8/487—Fluid loss control additives; Additives for reducing or preventing circulation loss
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/46—Water-loss or fluid-loss reducers, hygroscopic or hydrophilic agents, water retention agents
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • 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
    • C08F2810/00—Chemical modification of a polymer

Definitions

  • the present invention relates to a polyvinyl alcohol-based polymer and its use.
  • Polymers having a polyvinyl alcohol (PVA) skeleton are hydrophilic. It is known as a synthetic resin that has, and various uses that make the best use of its characteristics are being developed.
  • One such application is an additive to oil well cement used for cementing oil wells, gas wells, steam wells for geothermal power generation, etc.
  • the well cement is mixed with water and other additives, and is filled in the gap between the steel pipe and the well to fix and protect the steel pipe (casing) as a slurry. Therefore, it is preferable that the cement slurry has high fluidity so that it can be easily filled.
  • the loss of water content from the cement slurry due to the high pressure at the time of injection and the heat in the ground is generally referred to as "fluid loss". Fluid loss reduces the fluidity of the cement slurry, resulting in poor cementing and poor hardening after the cement has hardened. Therefore, a fluid loss reducing agent is usually added to the cement slurry.
  • Patent Documents 1 and 2 describe PVA used as a fluid loss reducing agent.
  • the present invention can provide the following.
  • aqueous solution of a polyvinyl alcohol-based polymer was filtered through a 100 mesh (opening 0.154 mm) filter, and then measured in an aqueous solution adjusted to a concentration of 10.0% by mass, in the region of an angular frequency of 1.0 to 10.0 rad / s.
  • a polyvinyl alcohol-based polymer characterized in that the slope when a log-log plot of a storage elastic modulus G'(20 ° C.) is 1.2 or less.
  • the value of the angular frequency-dependent loss tangent (tan ⁇ ) of the 10.0 mass% aqueous solution after filtration is 1.0 to 10.0 in the region where the angular frequency is 0.1 to 100 rad / s. It is preferably in the range of. Further, in some embodiments, the degree of saponification of the polyvinyl alcohol-based polymer is preferably 72 to 99 mol%. Further, in some embodiments, an additive for oil well cement containing a polyvinyl alcohol-based polymer can also be provided.
  • the polyvinyl alcohol-based polymer according to the present invention exhibits an excellent effect of reducing fluid loss even in a severe high temperature or high pressure environment.
  • a polymer is a definition of a polymer by the International Association of Genuine Applied Chemistry (IUPAC) Polymer Naming Methods Committee, that is, "a polymer molecule is a molecule having a large relative molecular mass and has a relative molecular mass. A unit having a structure composed of a large number of repetitions of a unit obtained from a small molecule substantially or conceptually. "
  • the polyvinyl alcohol-based polymer according to the present invention includes a homopolymer composed of a vinyl ester monomer, a copolymer of a vinyl ester monomer and a monofunctional monomer other than the vinyl ester, and a vinyl ester monomer.
  • the polyvinyl alcohol-based polymer according to the present invention has a polymer structure that can withstand high temperatures and pressures that cannot be tolerated by conventional PVA. Having such a polymer structure can be determined from the rheological properties of the polymer, and more specifically, it is ensured that the storage elastic modulus G'under specific conditions of PVA is within a predetermined range.
  • the present inventor finds that as the gel properties of PVA become stronger, the slopes of both G'' and G'log-log plots approach about 1 in a wide frequency region including the low frequency region, that is, tan ⁇ . I found that it wouldn't grow. Such findings are described, for example, in the following literature. References: https://aip.scitation.org/doi/abs/10.1063/1.1770590 The present inventor has found that by controlling the structure of PVA, a storage elastic modulus G'that cannot be obtained by conventional PVA can be obtained, and the present invention has been completed.
  • the vinyl ester monomer described above may be, for example, vinyl acetate, vinyl propionate, vinyl butyrate, vinyl valerate, vinyl caprate, vinyl laurate, vinyl stearate, vinyl benzoate, vinyl pivalate and the like. A mixture of these may be used. Vinyl acetate is preferable from the viewpoint of ease of polymerization.
  • examples of the monofunctional monomer copolymerizable with the vinyl ester monomer include the following compounds.
  • ⁇ -olefin monomers such as ethylene and propylene.
  • (Meta) Acrylic acid alkyl ester monomers such as (meth) methyl acrylate, (meth) ethyl acrylate, (meth) butyl acrylate, and (meth) 2-ethylhexyl acrylate.
  • Unsaturated amide monomers such as (meth) acrylamide and N-methylolacrylamide.
  • Unsaturated carboxylic acid monomers such as acrylic acid, crotonic acid, maleic acid, itaconic acid, and fumaric acid.
  • Anhydrate of unsaturated carboxylic acids such as maleic anhydride.
  • Salts of unsaturated carboxylic acids such as sodium, potassium and ammonium.
  • a sulfonic acid group-containing monomer such as 2-acrylamide-2-methylpropanesulfonic acid or a salt thereof.
  • Alkyl vinyl ether monomer Alkyl vinyl ether monomer.
  • a compound having two or more polymerizable unsaturated bonds in the molecule can be used.
  • Examples of such compounds include the following.
  • Divinyl ethers such as ethanediol divinyl ether, propanediol divinyl ether, butanediol divinyl ether, ethylene glycol divinyl ether, diethylene glycol divinyl ether, triethylene glycol divinyl ether, polyethylene glycol divinyl ether, propylene glycol divinyl ether, polypropylene glycol divinyl ether, and divinyl.
  • Divinyl ethers such as ethanediol divinyl ether, propanediol divinyl ether, butanediol divinyl ether, ethylene glycol divinyl ether, diethylene glycol divinyl ether, triethylene glycol divinyl ether, polyethylene glycol divinyl ether, propylene glycol divinyl ether, polypropylene
  • Diene compounds such as pentadiene, hexadiene, heptadiene, octadiene, nonadien, and decadien.
  • Dialyl ether compounds such as glycerin diallyl ether, diethylene glycol diallyl ether, ethylene glycol diallyl ether, triethylene glycol diallyl ether, polyethylene glycol diallyl ether, trimethylolpropanediallyl ether, pentaerythritol diallyl ether.
  • Triallyl ether compounds such as glycerin triallyl ether, trimethylolpropane triallyl ether, pentaerythritol triallyl ether.
  • Tetraallyl ether compounds such as pentaerythritol tetraallyl ether.
  • a polyfunctional monomer containing an allyl ester group such as diallyl phthalate, diallyl maleate, diallyl itaconic acid, diallyl terephthalate, and diallyl adipate.
  • a polyfunctional monomer containing a diallylamine compound such as diallylamine and diallylmethylamine, and an allylamino group such as triallylamine.
  • a polyfunctional monomer containing an allylammonium group such as a diallylammonium salt such as diallyldimethylammonium chloride.
  • a polyfunctional monomer containing two or more allyl groups such as triallyl isocyanurate, 1,3-diallyl urea, triallyl phosphate, and diallyl disulfide.
  • a polyfunctional monomer having (meth) acrylamide such as N, N'-methylenebis (meth) acrylamide and N, N'-ethylenebis (meth) acrylamide.
  • Polyfunctional aromatic monomers such as divinylbenzene and trivinylbenzene.
  • a glycidyl group-containing monomer such as allyl glycidyl ether and glycidyl (meth) acrylate.
  • the compound that can be copolymerized with the vinyl ester monomer is preferably a compound that is not easily decomposed by an alkali, and is a molecule.
  • Compounds having a carbonyl group or an amide group within are more preferable.
  • PVA is obtained by saponifying a copolymer of a vinyl ester monomer and a polyfunctional monomer to form a crosslinked structure from the polyfunctional group, so that it is resistant to dissolution at high temperatures. It has the effect of obtaining sex.
  • a polyfunctional monomer a compound having a ring structure is preferable, a compound having a heterocyclic structure is more preferable, and triallyl isocyanurate (TAIC) is particularly preferable.
  • the amount of copolymerization is 100 mol% of the structural unit derived from the vinyl alcohol unit in the vinyl alcohol-based polymer, and the simple amount other than the vinyl ester.
  • the structural unit derived from the polymer is preferably 0.001 to 1.0 mol%, more preferably 0.005 to 0.5 mol%, and more preferably 0.01 to 0.2 mol%. Is even more preferable.
  • the amount of copolymerization can be calculated using a trace total nitrogen analyzer.
  • a trace total nitrogen analyzer manufactured by Nittoseiko Analytech Co., Ltd.
  • it can be calculated by the following procedure.
  • a sample of vinyl alcohol polymer is collected on a quartz board, set in the auto boat controller ABC-210 (manufactured by Nittoseiko Analytech Co., Ltd.), automatically inserted into the electric furnace, and in an argon / oxygen stream. Burn with.
  • the NO gas generated at this time is measured by a chemiluminescence detector.
  • a calibration curve is prepared in advance with a standard solution (N-pyridine / toluene), and the nitrogen concentration is calculated from the calibration curve.
  • Any method can be used for the polymerization of the vinyl ester monomer or its copolymer, and known polymerization methods such as solution polymerization, suspension polymerization, and bulk polymerization may be used. From the viewpoint of ease of operation and the possibility of using a solvent common to the saponification reaction which is a subsequent step, it is preferable to use a solution polymerization method in alcohol, and it is particularly preferable to use methanol as the alcohol. preferable.
  • PVA can be prepared by saponifying the polymer obtained as described above by any method.
  • the saponification method include a method of adding an alkaline catalyst to an alcohol solution of a polymer (polyvinyl ester or the like).
  • an example of the saponification procedure will be described.
  • the alcohol that serves as a solvent for the polymer for example, methanol, ethanol, butanol, or the like can be used, and methanol can be preferably used.
  • the concentration of the polymer in the alcohol solution can be arbitrarily set, and may be, for example, 10% by mass or more and 80% by mass or less.
  • an alkaline catalyst is added to the above solution to perform a saponification reaction.
  • the alkali catalyst include alkali metal hydroxides such as sodium hydroxide, potassium hydroxide, sodium methylate, sodium ethyllate, and potassium methylate, and alcoholates. Among these, it is preferable to use sodium hydroxide.
  • the amount of the alkaline catalyst added is not particularly limited, but is preferably 1.0 to 100.0 mmol equivalent with respect to the polymer, and more preferably 5.0 to 30.0 mmol equivalent.
  • the reaction temperature at the time of saponification is not particularly limited, but is preferably 10 to 70 ° C, more preferably 30 to 55 ° C.
  • the reaction time is also not particularly limited, and may be, for example, 20 minutes or more to 2 hours.
  • the degree of saponification can be appropriately adjusted according to the use of PVA, and may be, for example, 72 to 99 mol%.
  • a washing step and a drying step for removing impurities such as sodium acetate may be performed, if necessary.
  • the above-mentioned PVA-containing additives for oil well cement can be provided and can be suitably used for cementing oil wells, gas wells, steam wells for geothermal power generation, and the like.
  • cementing performed when drilling a well is the work of injecting cement into the gap between the drilled well and the steel pipe inserted into it.
  • a cementing method a method is widely adopted in which cement and various additives such as fluid loss additives are mixed in a dry state and then pumped while being slurryed with high-pressure water.
  • PVA When PVA is used as a fluid loss reducing agent, it is possible to reduce the loss of water content from the cement slurry during cementing (that is, reduce fluid loss) and maintain the fluidity of the cement slurry. Will be. When the fluid loss is large, the fluidity of the cement slurry is lost and it becomes difficult to perform sufficient cementing.
  • Fluid Loss is one of the evaluation items of oil country cement defined by the American Petroleum Institute (API).
  • API American Petroleum Institute
  • the test method for fluid loss is described in Recommitted Practice for Testing Well Cement, API Recommitted Practice 10B-2, April 2013.
  • oil well cement composition for oil wells it is possible to provide an oil well cement composition containing the oil well cement and the above-mentioned oil well cement additive.
  • the oil well cement may be any cement used for cementing oil wells, gas wells, steam wells for geothermal power generation, and the like, and is not particularly limited.
  • the above composition preferably has an additive content for oil well cement of 0.01 to 10% boc, more preferably 0.05 to 5% boc. With such a range, fluid loss is effectively reduced.
  • "bwoc" by weight of cement means a cement weight standard, and refers to the weight of a dry additive added to a cement composition based only on the solid content of cement.
  • an oil well cement slurry containing oil well cement, the above-mentioned oil well cement additive, and water can also be provided.
  • the cement slurry preferably has a water content of 20 to 40% by mass.
  • the method of incorporating the oil country cement additive into the cement slurry is not particularly limited.
  • a method of preparing a composition containing an oil well cement and an additive and then mixing the composition with water a method of mixing an oil well cement, an additive and water without preparing a composition, and the like can be mentioned. Be done.
  • Example 1 In a polymerization can equipped with a reflux condenser, a dropping funnel, and a stirrer, 100 parts by mass of vinyl acetate, 67 parts by mass of methanol, 0.16 parts by mass of triallyl isocyanurate (TAIC) as a polyfunctional monomer, as an initiator.
  • TAIC triallyl isocyanurate
  • Parloyl NPP manufactured by Nippon Oil & Fats Co., Ltd.
  • polymerization was carried out at a boiling point for 5.0 hours while stirring in a nitrogen atmosphere.
  • the unreacted vinyl acetate monomer was removed from the polymerization system to obtain a methanol solution of the polyvinyl acetate-TAIC copolymer.
  • a methanol solution of sodium hydroxide was added to the methanol solution of the obtained vinyl acetate-TAIC copolymer (0.008 mol% of sodium hydroxide with respect to the copolymer). Then, the saponification reaction was carried out at 45 ° C. for 45 minutes to obtain PVA having a saponification degree of 88.2 mol%.
  • a PVA aqueous solution of 10% by mass or more was prepared, and the solution was filtered with a 100 mesh (opening 0.154 mm) filter.
  • the concentration of the aqueous solution after filtration was measured, and when the concentration was 10% by mass or more, pure water was added to adjust the concentration to 10% by mass.
  • the dynamic viscoelasticity of the prepared solution was measured using a rheometer measuring device (Anton Paar MCR).
  • the plate used was a cone plate CP50-2 (diameter: 50 mm, angle 2 °).
  • the measurement conditions are temperature 30 ° C., shear strain (vibration) 1 ⁇ 5% (logous slope), angular frequency 628.3 ⁇ 0.06 rad / s (linear slope), storage elastic modulus G'and loss elastic modulus G'. 'Get.
  • the loss tangent (tan ⁇ ) was calculated by (loss elastic modulus G ′′ / storage elastic modulus G ′).
  • Class G well cement is blended with the amounts shown in Table 1 and a curing retarder (CR-270, manufactured by Flotek Industries) 0.4bwoc, and the American Petroleum Association (API) standard 10B-2 (April 2013). ), These were mixed with water to obtain a cement slurry having a water content of 30% by mass.
  • the obtained cement slurry was put into a fluid loss evaluation tester (Model 7120, Standard Engineering), and is shown in Table 1 according to the procedure described in American Petroleum Institute (API) Standard 10B-2 (April 2013). The test was carried out at the temperature of 1000 psi under a pressure of 1000 psi, and the amount of fluid loss was calculated.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Ceramic Engineering (AREA)
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  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Structural Engineering (AREA)
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  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
PCT/JP2021/026688 2020-07-31 2021-07-15 ポリビニルアルコール系重合体 Ceased WO2022024791A1 (ja)

Priority Applications (5)

Application Number Priority Date Filing Date Title
ES21850134T ES3032513T3 (en) 2020-07-31 2021-07-15 Polyvinyl alcohol-based polymer
CN202180035703.6A CN115698098A (zh) 2020-07-31 2021-07-15 聚乙烯醇系聚合物
US17/927,523 US12448469B2 (en) 2020-07-31 2021-07-15 Polyvinyl alcohol-based polymer
EP21850134.4A EP4144769B1 (en) 2020-07-31 2021-07-15 Polyvinyl alcohol-based polymer
JP2022540172A JP7561854B2 (ja) 2020-07-31 2021-07-15 ポリビニルアルコール系重合体

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JP2020131225 2020-07-31
JP2020-131225 2020-07-31

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2023238675A1 (https=) * 2022-06-08 2023-12-14
WO2026063163A1 (ja) * 2024-09-18 2026-03-26 デンカ株式会社 塗料用添加剤および水性塗料組成物

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JPS55104301A (en) * 1979-02-02 1980-08-09 Kureha Chem Ind Co Ltd Hydrophilic nonionic rigid gel
JP2000157625A (ja) * 1998-11-26 2000-06-13 Seed Co Ltd ポリビニルアルコール製医療用ヒドロゲル及びその製造方法
WO2007146348A2 (en) 2006-06-13 2007-12-21 Celanese International Corporation Fluid loss additive with improved rheological properties
JP2015196733A (ja) 2014-03-31 2015-11-09 株式会社クラレ スラリー用添加剤、掘削泥水及びセメントスラリー
WO2019163490A1 (ja) * 2018-02-22 2019-08-29 デンカ株式会社 油井セメント用添加剤及び該油井セメント用添加剤を用いたセメントスラリー
WO2021116678A1 (en) * 2019-12-09 2021-06-17 Synthomer (Uk) Limited Improvements in, or relating to, binders and/or coatings

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EP4144769A4 (en) 2023-11-08
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CN115698098A (zh) 2023-02-03
EP4144769A1 (en) 2023-03-08
TWI906335B (zh) 2025-12-01
JPWO2022024791A1 (https=) 2022-02-03
US20230242687A1 (en) 2023-08-03
TW202216636A (zh) 2022-05-01
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