JP4616628B2 - Solid polymer electrolyte membrane using phosphate esterified unsaturated alcohol copolymer and use thereof - Google Patents

Description

The present invention, proton conductivity, excellent balance of water resistance and solvent resistance, relates to fuel cells as low-cost solid polymer electrolyte membrane and use thereof.

  Polymers belonging to so-called cation exchange resins such as polystyrene sulfonic acid, polyvinyl sulfonic acid, perfluorosulfonic acid polymer, perfluorocarboxylic acid polymer [Polymer Preprints, Japan Vol. 42, No. 7, pp. 2490-2492 (1993), Polymer Preprints, Japan Vol. 43, No. 3, pp. 735-736 (1994), Polymer Preprints, Japan Vol. 42, No. 3, p. 730 (1993)] etc. Has been reported.

  In particular, a solid polymer material having a sulfonic acid group in the side chain has a property of binding firmly to a specific ion or selectively transmitting a cation or an anion. It is formed into a shape or a membrane and is used in various applications such as electrodialysis membranes, diffusion dialysis membranes, and battery membranes. Above all, the fluorine-based polymer electrolyte membrane having a sulfonic acid group in the side chain of the perfluoro skeleton known by the trademark Nafion (manufactured by DuPont) has excellent heat resistance and chemical resistance and can be used under severe conditions. It has been put to practical use as an electrolyte membrane that can withstand use. However, the fluorine-based electrolyte membrane as described above has a problem that it is very expensive.

  By the way, the proton conducting solid electrolyte operating at room temperature is required to have sufficient water absorption even for an alternative material because protons are transported at a high speed by the action of water contained in the solid. In particular, many are used in wet environments, so they must also have water resistance. In conventional perfluorosulfonic acid electrolytes, water absorbed around the highly hydrophilic sulfonic acid group carries ions at a high speed, and the polyfluoroethylene skeleton has water resistance, chemical stability, high temperature durability, etc. Plays the role of maintaining.

  Polyvinyl alcohol (PVA) is an example of a highly hydrophilic and inexpensive hydrocarbon polymer material, and a material with proton conductivity mixed with phosphoric acid can be used as a proton conductive solid electrolyte. is there. This solid electrolyte can move protons at high speed due to the high water absorption of PVA. However, since PVA is easily dissolved in water, there is a problem that the material stability in a wet environment is low.

  JP 2003-7133 (Patent Document 1) is obtained by neutralizing an aqueous solution in which an alkali metal salt of silicic acid, phosphoric acid and PVA are dissolved, removing water as a solvent, and removing unnecessary salts. We have proposed an ion-conducting solid electrolyte consisting of water-containing silicic acid compound, phosphoric acid compound and PVA. This ion conductive solid electrolyte has both water resistance by a silicic acid compound and water absorption by PVA, and is inexpensive. However, since the ion conductive solid electrolyte of Patent Document 1 contains a silicate compound, there is a problem that thin film processing is difficult. In order to improve the water resistance of PVA, there is a method of adding a water resistant resin such as polyvinyl chloride, but PVA and polyvinyl chloride have poor compatibility.

  Japanese Patent Laid-Open No. 2004-185891 (Patent Document 2) discloses a polymer electrolyte obtained by mixing polyvinyl phosphate (a polymer having a structure in which the hydroxyl group of PVA is substituted with a phosphate group) and a basic molecule (such as imidazole). A membrane is proposed. In this membrane, since basic molecules serve as a proton conduction medium, the membrane exhibits proton conductivity even without humidification, and does not require a humidifier. However, free acid generated from the polymer electrolyte membrane may cause a system failure when the fuel cell is operated.

  With regard to the method of phosphoric esterifying an unsaturated alcohol copolymer, the present applicant has previously described an unsaturated alcohol copolymer, a phosphoric acid source compound, and water in an organic solvent having no hydroxyl group. Proposed a method of reacting with (No. 2004-307196). However, the phosphate esterified unsaturated alcohol copolymer obtained by this method may have an insufficient hue, and it is desired to improve the hue when used in applications such as paints, paper and pulp modifiers.

JP2003-7133 JP2004-185891

  Accordingly, an object of the present invention is to provide an inexpensive solid polymer electrolyte membrane having an excellent balance of proton conductivity, water resistance and solvent resistance.

As a result of intense research in view of the above object, the present inventors, the solid polymer containing a vinyl copolymer with an unsaturated alcohol copolymer were phosphorylated and the other conductive resins containing fatty acid vinyl unit The electrolyte membrane was found to have an excellent balance of electrical conductivity, water resistance and solvent resistance, and the present invention was conceived.

で表される繰り返し単位(I)、及び式(II)：

で表される繰り返し単位(II)からなり、前記繰り返し単位(I)及び(II)の合計を100モル％として前記繰り返し単位(I)の割合が５〜60モル％であり、平均重合度が100〜3,000である不飽和アルコール系共重合体と、(b) 無水リン酸と、(c) 水又は過酸化水素水とを反応させてなり、もって前記不飽和アルコール系共重合体の水酸基の少なくとも一部を-OP(O)(OH) ₂ 基で置換してなる化合物であり、
前記他の導電性樹脂(B)は、ホスホン酸基含有（メタ）アクリルアミド誘導体(B-1)、リン酸基含有不飽和単量体(B-2)、スルホン酸基含有不飽和単量体(B-3)、並びにアルコール性水酸基含有不飽和単量体のリン酸エステル化物(B-4)からなる群から選ばれた少なくとも一種の酸性基含有不飽和単量体を少なくとも重合してなる化合物であり、
前記ホスホン酸基含有（メタ）アクリルアミド誘導体(B-1)は、（メタ）アクリルアミドホスホン酸、（メタ）アクリルアミドジホスホン酸及びホスホン酸基含有ターシャリーブチルアクリルアミドスルホン酸からなる群から選ばれた少なくとも一種であり、
前記リン酸基含有不飽和単量体(B-2)は、(B-2-1) 式(13):

（ただしR ¹⁰ は水素又はメチル基であり、R ¹¹ は水素又は置換もしくは無置換のアルキル基であり、pは１〜６の整数である。）により表されるリン酸基含有モノエステル不飽和単量体、又は(B-2-2) 前記リン酸基含有モノエステル不飽和単量体と、式(14):

（ただしR ¹⁰ 及びR ^10' はそれぞれ独立に水素基又はメチル基であり、R ¹¹ 及びR ^11' はそれぞれ独立に水素基又は置換もしくは無置換のアルキル基であり、p'及びp''はそれぞれ独立に１〜６の整数である。）により表されるリン酸基含有ジエステル不飽和単量体、及び式(15):

（ただしR ¹⁰ 及びR ^10' はそれぞれ独立に水素基又はメチル基であり、R ¹¹ 及びR ^11' はそれぞれ独立に水素基又は置換もしくは無置換のアルキル基であり、p'及びp''はそれぞれ独立に１〜６の整数である。）により表されるピロリン酸基含有不飽和単量体のいずれかもしくはこれらの両方との混合物であり、
前記スルホン酸基含有不飽和単量体(B-3)は、ターシャリーブチルアクリルアミドスルホン酸、アリルスルホン酸、メタアリルスルホン酸、ビニルスルホン酸、p-スチレンスルホン酸、（メタ）アクリル酸ブチル-4-スルホン酸又は（メタ）アクリロオキシベンゼンスルホン酸であり、
前記アルコール性水酸基含有不飽和単量体のリン酸エステル化物(B-4)は、グリセロールジ（メタ）アクリレート、1,6-ヘキサンジオールジグリシジルエーテルアクリレート、1,4-ブタンジオールジグリシジルエーテルアクリレート、ビスフェノールA型エポキシアクリレート、及び2-ヒドロキシ（メタ）アクリレートのうちのいずれかのリン酸エステル化物であり、
前記非導電性樹脂(C)は、メラミン樹脂、ポリビニルアルコール、ポリ（メタ）アクリロニトリル、ポリ（メタ）アクリル酸エステル、ポリアクリルアミド、ポリアセタール、水溶性ウレタン樹脂、セルロース、ポリスチレン、ポリ塩化ビニル、ポリ酢酸ビニル、ビニル芳香族−共役ジエン系共重合体、共役ジエン系液状オリゴマーの重合体、アルキルアミノ基含有不飽和単量体の重合体、及びフッ素基含有不飽和単量体の重合体からなる群から選ばれた少なくとも一種であり、
前記共役ジエン系液状オリゴマーは、式(19)：

（但しR ¹⁴ 及びR ¹⁵ はそれぞれ独立に(a) エチレン性不飽和結合を１個以上有し、かつ他の原子団を有してもよい炭化水素基、(b) エチレン性不飽和結合を有さず、かつ他の原子団を有してもよい炭化水素基又は(c) 水素基であり、かつR ¹⁴ 及びR ¹⁵ の少なくとも一方は前記(a) エチレン性不飽和結合を有する炭化水素基であり、R ¹⁶ 及びR ¹⁷ はそれぞれ独立に水素基又はメチル基であり、かつR ¹⁶ 及びR ¹⁷ の少なくとも一方は水素基であり、tは重合度を表す。）により表され、
前記アルキルアミノ基含有不飽和単量体は、N,N-ジアルキル（メタ）アクリルアミド、ジメチルアミノエチル（メタ）アクリレート、ジエチルアミノエチル（メタ）アクリレート、ジメチルアミノプロピル（メタ）アクリレート、ジメチルアミノブチル（メタ）アクリレート、ジプロピルアミノエチル（メタ）アクリレート、ジブチルアミノエチル（メタ）アクリレート、ジメチルアミノエチル（メタ）アクリルアミド、ジエチルアミノエチル（メタ）アクリルアミド、ジメチルアミノプロピル（メタ）アクリルアミド、ジメチルアミノブチル（メタ）アクリルアミド、ジプロピルアミノエチル（メタ）アクリルアミド、又はジブチルアミノエチル（メタ）アクリルアミドであり、
前記フッ素基含有不飽和単量体は、ハイドロフルオロアルキル基含有（メタ）アクリル酸エステル、パーフルオロアルキル基含有（メタ）アクリル酸エステル、ハイドロフルオロアルキル基含有ビニル、又はパーフルオロアルキル基含有ビニルである
ことを特徴とする。
Solid polymer electrolyte membrane of the present invention, (1) phosphoric acid esterified unsaturated alcohol copolymer polymer (A), the first composition comprising the other of the conductive resin (B), or (2 ) Proton conductivity comprising a second composition comprising the phosphate esterified unsaturated alcohol copolymer (A), the other conductive resin (B), and the non-conductive resin (C) . A solid polymer electrolyte membrane having
The phosphate esterified unsaturated alcohol copolymer (A) comprises (a) Formula (I):

The repeating unit (I) represented by the formula (II):

The total of the repeating units (I) and (II) is 100 mol%, the ratio of the repeating units (I) is 5 to 60 mol%, and the average degree of polymerization is 100 to 3,000 unsaturated alcohol copolymer, (b) anhydrous phosphoric acid, and (c) water or hydrogen peroxide solution are reacted to form a hydroxyl group of the unsaturated alcohol copolymer. It is a compound formed by substituting at least a part with -OP (O) (OH) ₂ group,
The other conductive resin (B) includes a phosphonic acid group-containing (meth) acrylamide derivative (B-1), a phosphoric acid group-containing unsaturated monomer (B-2), and a sulfonic acid group-containing unsaturated monomer. (B-3) and at least one acidic group-containing unsaturated monomer selected from the group consisting of phosphate esterified products of alcoholic hydroxyl group-containing unsaturated monomers (B-4) A compound,
The phosphonic acid group-containing (meth) acrylamide derivative (B-1) is at least selected from the group consisting of (meth) acrylamide phosphonic acid, (meth) acrylamide diphosphonic acid and phosphonic acid group-containing tertiary butyl acrylamide sulfonic acid. A kind,
The phosphate group-containing unsaturated monomer (B-2) is represented by (B-2-1) formula (13):

(Wherein R ¹⁰ is hydrogen or a methyl group, R ¹¹ is hydrogen or a substituted or unsubstituted alkyl group, and p is an integer of 1 to 6). A monomer, or (B-2-2) the phosphoric acid group-containing monoester unsaturated monomer, and the formula (14):

(However, R ¹⁰ and R ^{10 ′} are each independently a hydrogen group or a methyl group, R ¹¹ and R ^{11 ′} are each independently a hydrogen group or a substituted or unsubstituted alkyl group, and p ′ and p ″ are Each independently represents an integer of 1 to 6. The phosphoric acid group-containing diester unsaturated monomer represented by formula (15):

(However, R ¹⁰ and R ^{10 ′} are each independently a hydrogen group or a methyl group, R ¹¹ and R ^{11 ′} are each independently a hydrogen group or a substituted or unsubstituted alkyl group, and p ′ and p ″ are Each independently an integer of 1 to 6), or any of the pyrophosphate group-containing unsaturated monomers represented by
The sulfonic acid group-containing unsaturated monomer (B-3) includes tertiary butyl acrylamide sulfonic acid, allyl sulfonic acid, methallyl sulfonic acid, vinyl sulfonic acid, p-styrene sulfonic acid, butyl (meth) acrylate, 4-sulfonic acid or (meth) acryloxybenzenesulfonic acid,
The alcoholic hydroxyl group-containing unsaturated monomer phosphate ester (B-4) comprises glycerol di (meth) acrylate, 1,6-hexanediol diglycidyl ether acrylate, 1,4-butanediol diglycidyl ether acrylate , Bisphenol A type epoxy acrylate, and 2-hydroxy (meth) acrylate phosphoric acid ester,
The non-conductive resin (C) is melamine resin, polyvinyl alcohol, poly (meth) acrylonitrile, poly (meth) acrylic acid ester, polyacrylamide, polyacetal, water-soluble urethane resin, cellulose, polystyrene, polyvinyl chloride, polyacetic acid A group consisting of vinyl, vinyl aromatic-conjugated diene copolymer, polymer of conjugated diene liquid oligomer, polymer of alkylamino group-containing unsaturated monomer, and polymer of fluorine-containing unsaturated monomer At least one kind selected from
The conjugated diene-based liquid oligomer has the formula (19):

(However, R ¹⁴ and R ¹⁵ are each independently (a) a hydrocarbon group which has one or more ethylenically unsaturated bonds and may have other atomic groups, and (b) an ethylenically unsaturated bond. A hydrocarbon group which does not have and may have another atomic group or (c) a hydrogen group, and at least one of R ¹⁴ and R ¹⁵ has (a) a hydrocarbon having an ethylenically unsaturated bond R ¹⁶ and R ¹⁷ are each independently a hydrogen group or a methyl group, and at least one of R ¹⁶ and R ¹⁷ is a hydrogen group, and t represents the degree of polymerization.
The alkylamino group-containing unsaturated monomer includes N, N-dialkyl (meth) acrylamide, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (meth) acrylate, dimethylaminopropyl (meth) acrylate, dimethylaminobutyl (meth) ) Acrylate, dipropylaminoethyl (meth) acrylate, dibutylaminoethyl (meth) acrylate, dimethylaminoethyl (meth) acrylamide, diethylaminoethyl (meth) acrylamide, dimethylaminopropyl (meth) acrylamide, dimethylaminobutyl (meth) acrylamide , Dipropylaminoethyl (meth) acrylamide, or dibutylaminoethyl (meth) acrylamide,
The fluorine group-containing unsaturated monomer is hydrofluoroalkyl group-containing (meth) acrylic acid ester, perfluoroalkyl group-containing (meth) acrylic acid ester, hydrofluoroalkyl group-containing vinyl, or perfluoroalkyl group-containing vinyl. It is characterized by being.

The phosphate esterified unsaturated alcohol copolymer preferably forms an ammonium salt, an amine salt or a metal salt. As metal salts, alkali metal salts such as potassium salts, cuprous oxide (reddish brown), cupric oxide (blue), equimolar mixture of cuprous oxide (1) and cupric salt (gray), oxidation Heavy metal salts such as ferric salt (brown) are preferred. Although these heavy metal salts are slightly colored, they are particularly useful as proton conductive solid polymer electrolyte membranes because they are particularly highly conductive, do not gel, and can be formed into membranes.

The conductive resin (B), together with the acidic group-containing unsaturated monomers, (meth) acrylonitrile, the conjugated diene-based liquid oligomer or hydrides thereof, the alkyl amino group-containing unsaturated monomers, (meth) acrylate acid ester le, styrene emission, vinyl chloride, vinyl acetate, the fluorinated group-containing unsaturated monomer, a vinyl aromatic - conjugated diene copolymer, ethylene glycol di (meth) acrylate, trimethylolpropane tri (meth) A compound that does not contain at least one acidic group selected from the group consisting of acrylate, divinylbenzene, and urethane acrylate obtained by reacting diisocyanate with glycerol di (meth) acrylate may be included as a copolymerization component. The mass ratio of the acidic group-containing unsaturated monomer and the acidic group-free compound is preferably 50/50 or more. In a preferred example of the present invention, the acidic group-containing unsaturated monomer of the other conductive resin (B) is the phosphonic acid group-containing (meth) acrylamide derivative (B-1) and the alcoholic hydroxyl group-containing It consists of a phosphorylated ester (B-4) of a saturated monomer. In another preferred example of the present invention, the non-acidic group-containing compound of the other conductive resin (B) is composed of (meth) acrylonitrile, the conjugated diene-based liquid oligomer, and the alkylamino group-containing unsaturated monomer. Become. The conjugated diene liquid oligomer is preferably a butadiene oligomer having at least two ethylenically unsaturated bonds in the molecule. The alkylamino group-containing unsaturated monomer is preferably N, N-dimethylacrylamide. The vinyl aromatic-conjugated diene copolymer is preferably a styrene-isoprene copolymer.

  The solid polymer electrolyte membrane of the present invention is suitable for fuel cell applications.

Solid polymer electrolyte membrane of the present invention contain a vinyl copolymer obtained by phosphorylation of the unsaturated alcohol copolymer containing fatty acid vinyl unit and the other conductive resins, proton conductivity, water Excellent balance of solvent and solvent resistance. The solid polymer electrolyte membrane of the present invention has (1) a hydrophobic portion composed of a hydrocarbon skeleton in which vinyl groups are linked in a chain, and (2) a hydrophilic portion composed of a phosphate group and an unreacted hydroxyl group. The hydrophilic part is presumed to be an efficient proton conduction path. Moreover, since the solid polymer electrolyte membrane of this invention has a fatty-acid vinyl unit, it is thought that this has expressed water resistance and solvent resistance.

  The solid polymer electrolyte membrane of the present invention having such characteristics includes an electrolyte membrane for a primary battery, an electrolyte membrane for a secondary battery, an electrolyte membrane for a fuel cell, a display element membrane, various sensor membranes, a signal transmission medium membrane, a solid capacitor It can be suitably used for membranes, ion exchange membranes and the like. Especially when used as an electrolyte membrane in a direct methanol solid polymer fuel cell, the hydrophobic part exhibits excellent methanol crossover prevention (capability to prevent methanol from passing through the solid polymer electrolyte membrane) Presumed to be.

[1] Method for Producing Phosphate Estered Unsaturated Alcohol Copolymer A method for producing a phosphate esterified unsaturated alcohol copolymer of the present invention comprises an unsaturated alcohol copolymer, a phosphoric acid source compound, , To react with hydrogen peroxide solution.
(1) Unsaturated alcohol copolymer The unsaturated alcohol copolymer contains at least an unsaturated alcohol unit and a fatty acid vinyl unit. Examples of the unsaturated alcohol unit include a vinyl alcohol unit and an allyl alcohol unit, and a vinyl alcohol unit is preferable from the viewpoint of production cost. Vinyl alcohol does not exist as a monomer, but exists as a constituent unit of an unsaturated alcohol copolymer. In order to obtain vinyl alcohol units, an unsaturated alcohol copolymer containing vinyl acetate units may be prepared and saponified.

（但しR¹はアルキル基であり、n及びmは各々重合度である。）により表すことができる。 The unsaturated alcohol copolymer having a vinyl alcohol unit is represented by the following general formula (1):

(Wherein R ¹ is an alkyl group, and n and m are degrees of polymerization, respectively).

  Examples of the fatty acid vinyl unit include a vinyl acetate unit, a vinyl propinate unit, and a vinyl butyrate unit, and a vinyl acetate unit is preferable. Each of the unsaturated alcohol unit and the fatty acid vinyl unit may contain two or more kinds.

  The ratio of the unsaturated alcohol unit in the unsaturated alcohol copolymer is not particularly limited, but the total of the vinyl monomer units constituting the unsaturated alcohol copolymer is 100 mol%, and 5 to 60 mol%. It is preferable that 20 to 50 mol% is more preferable. When this proportion is less than 5 mol%, the amount of hydroxyl group required for the phosphoric esterification is small.

  The ratio of the fatty acid vinyl unit is not particularly limited, but the total amount of vinyl monomer units constituting the unsaturated alcohol copolymer is 100 mol%, preferably 40 to 95 mol%, more preferably 50 to 80 mol%. preferable. The unsaturated alcohol copolymer is excellent in water resistance and solvent resistance due to the alkyl group of the fatty acid vinyl unit.

  The unsaturated alcohol copolymer can be prepared by preparing a polymer of fatty acid vinyl or a monomer composition containing the same and partially saponifying it. The average degree of polymerization of the unsaturated alcohol copolymer is not particularly limited, but is preferably 100 to 3,000.

  Commercially available products may be used as the unsaturated alcohol copolymer. Examples of polyvinyl alcohols having vinyl acetate units include Kuraray LM Polymer and Poval (registered trademark, manufactured by Kuraray Co., Ltd.), Gohsenol (registered trademark, Nippon Synthetic Chemical). Kogyo Co., Ltd.). The saponification degree of the polyvinyl alcohol having a vinyl acetate unit is preferably 5 to 60, and more preferably 20 to 50.

  The unsaturated alcohol copolymer may contain other unsaturated monomer units. Other unsaturated monomers include (i) an unsaturated monomer having one or more ethylenically unsaturated bonds and acidic groups in the molecule, and (ii) one or more ethylenically unsaturated monomers in the molecule. It is roughly classified into unsaturated monomers having a saturated bond but not having an acidic group. The unsaturated monomer having an acidic group preferably has at least one acidic group selected from the group consisting of a phosphoric acid group, a sulfonic acid group, a carboxylic acid group, and an alcoholic hydroxyl group. Examples of unsaturated monomers having no acidic group include (meth) acrylonitrile, (meth) acrylic acid esters, (meth) acrylic acid amides, alkylamino group-containing unsaturated monomers, substituted or unsubstituted styrenes , Vinyls, olefins (for example, ethylene), dienes and the like.

(2) Phosphate esterification method The unsaturated alcohol copolymer is converted to a phosphate by reacting the unsaturated alcohol copolymer with a phosphoric acid source compound and hydrogen peroxide. As the phosphoric acid source compound, phosphoric anhydride (P ₂ O ₅ ) is preferable. The blending ratio of P ₂ O ₅ with respect to 1 equivalent of the hydroxyl group of the unsaturated alcohol copolymer may be appropriately set according to the desired degree of phosphate esterification. The amount is preferably 0.5 mol or more per 1 equivalent. The upper limit of the blending ratio is preferably 1 mol or less.

Although there is no restriction | limiting in particular in the density | concentration of hydrogen peroxide water, For example, it is 1-20 mass%. The blending ratio of the hydrogen peroxide solution is preferably 1 to 3 mol, more preferably 1.3 to 1.8 mol, with respect to 1 mol of P ₂ O ₅ . By using hydrogen peroxide water, the hue of the resulting phosphate esterified unsaturated alcohol copolymer is improved.

  The reaction procedure is described. First, a solution composed of [unsaturated alcohol copolymer + solvent] is charged into a reactor equipped with a stirrer and a reflux condenser, and the temperature is raised to 30 to 70 ° C. At this time, a known polymerization inhibitor such as hydroquinone monomethyl ether or paramethoxyhydroquinone may be added together. After reaching a predetermined temperature, phosphoric anhydride and hydrogen peroxide are added. It is preferable that phosphoric anhydride and aqueous hydrogen peroxide are added in portions 2 to 10 times within 1 to 7 hours. Thereby, the phosphoric acid esterification reaction is promoted. However, it is not intended to be limited to the divided addition, and may be added in small portions continuously as necessary. Thereafter, the temperature is kept at 30 to 70 ° C., and the reaction is continued for 1 to 5 hours. The resulting reaction solution is cooled to room temperature. When inorganic polyphosphoric acid or the like by-produced by cooling is deposited, the solid deposited by natural filtration or suction filtration is separated by filtration.

（但しR²は水素又はメチル基であり、R³及びR⁴はそれぞれ独立にアルキル基を表す。）により表されるN,N-ジアルキル（メタ）アクリルアミド、ジメチルホルムアミド（DMF）、N,N-ジメチルアセトアミド（DMAc）等のアミド系溶媒、及びテトラヒドロフラン（THF）等が好ましい。これらの溶媒は、単独で用いてもよいし、二種以上を併用してもよい。 As the solvent, an organic solvent having no hydroxyl group is preferable. As such an organic solvent, the following formula (2):

(Wherein R ² is hydrogen or a methyl group, and R ³ and R ⁴ each independently represents an alkyl group.) N, N-dialkyl (meth) acrylamide, dimethylformamide (DMF), N, N An amide solvent such as dimethylacetamide (DMAc) and tetrahydrofuran (THF) are preferred. These solvents may be used alone or in combination of two or more.

Among them, the solvent is preferably at least one selected from the group consisting of N, N-dialkyl (meth) acrylamide, DMF, and THF. The alkyl group represented by R ³ and R ^{4 of} N, N-dialkyl (meth) acrylamide preferably has 2 or less carbon atoms. Among these, N, N-dimethylacrylamide (DMAA) and N, N-dimethylmethacrylamide are more preferable as N, N-dialkyl (meth) acrylamide. N, N-dialkyl (meth) acrylamide has an ethylenically unsaturated group, and after the phosphoric esterification reaction, radical polymerization is carried out by adding a polymerization initiator, thereby producing a phosphoric ester unsaturated alcoholic copolymer. And a mixed resin composition. Therefore, when N, N-dialkyl (meth) acrylamide is used alone as a solvent, it is not necessary to remove the solvent after the phosphoric acid esterification reaction.

  In order to accelerate the reaction and suppress the formation of by-products, the reaction solution preferably has an initial concentration before addition of phosphoric anhydride (the concentration of the unsaturated alcohol copolymer raw material) of 20 to 50% by mass. 25 to 40% by mass is more preferable. Although the viscosity increases due to the reaction between the raw material polymer and phosphoric anhydride, the viscosity may be lowered by adding a solvent as necessary.

  In order to remove unreacted phosphoric anhydride, by-product inorganic polyphosphoric acid, and the like, the solution after the reaction is filtered through a wire mesh or the like. The obtained crude resin is washed with a poor solvent for this. Washing is performed by adding a poor solvent to the solution after the filtration, stirring, precipitating the resin, and filtering. You may repeat the said washing | cleaning operation as needed. Examples of the poor solvent include chloroform, trichlene, xylene, n-hexane and the like. When the resin cannot be precipitated, it is preferable to place the filtered solution in a cellulose tube or the like and dialyze with pure water. The precipitated resin after washing is dried or the solvent is distilled off from the reaction solution after dialysis to isolate the phosphate esterified unsaturated alcohol copolymer.

（但しR¹はアルキル基であり、n及びmは各々重合度である。）により表すことができる。 (3) Phosphate esterified unsaturated alcohol copolymer The phosphoric esterified unsaturated alcohol copolymer thus obtained is obtained from, for example, an unsaturated alcohol copolymer represented by the above formula (1) as a raw material. When all the hydroxyl groups are converted to phosphoric acid esters, the following general formula (3):

(Wherein R ¹ is an alkyl group, and n and m are degrees of polymerization, respectively).

  The phosphate esterified unsaturated alcohol copolymer obtained by the production method of the present invention is excellent in hue. Specifically, the hue value measured by the Gardner method is 0.5 to 1.5. Moreover, the phosphate esterified unsaturated alcohol copolymer obtained by the production method of the present invention has an excellent balance of conductivity, water resistance and solvent resistance and is inexpensive. Phosphate-esterified unsaturated alcohol copolymers having such properties are useful for various applications such as conductive resins, antistatic agents, antifogging materials, paper / pulp modifiers, paints, coating agents, etc. is there.

  The phosphate esterified unsaturated alcohol copolymer may be converted into a complex salt if necessary, thereby improving conductivity and heat resistance. The complex salt is preferably an ammonium salt, an amine salt or a metal salt. When an ammonium salt or an amine salt is formed, in order to neutralize the charge, for example, an ammonium ion or mono-containing compound containing a primary, secondary, tertiary or quaternary alkyl group, allyl group, aralkyl group, etc. It is preferable to form a complex salt with a di- or trialkanolamine residue. As metal salts, alkali metal salts such as potassium salts, cuprous oxide (reddish brown), cupric oxide (blue), equimolar mixture of cuprous oxide (1) and cupric salt (gray), oxidation Heavy metal salts such as ferric salt (brown) are preferred. Although these heavy metal salts are slightly colored, they are particularly useful as proton conductive solid polymer electrolyte membranes because they are particularly highly conductive, do not gel, and can be formed into membranes. These complex salts may be used alone or in combination.

[2] Solid polymer electrolyte membrane The first solid polymer electrolyte membrane of the present invention comprises a vinyl copolymer obtained by phosphorylating the unsaturated alcohol copolymer. The second solid polymer electrolyte membrane of the present invention comprises (a) the same phosphate esterified unsaturated alcohol copolymer as the first solid polymer electrolyte membrane, and (b) another conductive resin and / or It consists of a uniform composition containing a non-conductive resin.

Since the unsaturated alcohol copolymer as a raw material is as described above, the description thereof is omitted. About the phosphoric acid esterification method of an unsaturated alcohol type copolymer, it is not limited to hydrolyzing with hydrogen peroxide water, It is the same as the above except that it may hydrolyze using only water. When only water is used for hydrolysis, the blending ratio is preferably 1 to 3 moles, more preferably 1.3 to 1.8 moles per mole of P ₂ O ₅ . If this blending ratio is less than 1 mole with respect to 1 mole of P ₂ O ₅ , a gelled product is likely to occur.

(1) First solid polymer electrolyte membrane The first solid polymer electrolyte membrane was prepared by preparing a polymer solution containing a phosphoric esterified unsaturated alcohol copolymer and a solvent, and placing the polymer solution horizontally. It is obtained by casting on a material (glass plate, polyolefin film, etc.), evaporating the solvent, and then heating to 50 to 140 ° C. Examples of the solvent include DMF, THF, lower alcohols and the like. It is preferable that the resin solid content concentration of the polymer solution is 5 to 30% by mass. The thickness of the cast film is usually 20 to 500 μm, preferably about 20 to 200 μm. The mechanical strength can be increased by further stretching the cast film thus formed. Stretching preferably involves heating.

(2) Second solid polymer electrolyte membrane The second solid polymer electrolyte membrane comprises (a) a phosphoric esterified unsaturated alcohol copolymer, (b) other conductive resin and / or non- It consists of a uniform composition containing a conductive resin.
(A) Other conductive resin The other conductive resin is preferably obtained by polymerizing an unsaturated monomer containing an acidic group. Further, the other conductive resin may contain an unsaturated monomer or oligomer each not containing an acidic group as a copolymerization component, if necessary. Hereinafter, the unsaturated monomer containing an acidic group, the unsaturated monomer not containing an acidic group, and an oligomer will be described.

(A-1) Unsaturated monomer containing acidic group and alcoholic hydroxyl group An unsaturated monomer containing an acidic group has at least one acidic group and at least one ethylenically unsaturated bond in the molecule. It is a compound that has. The acidic group is preferably at least one selected from the group consisting of phosphorus acid residues (for example, phosphonic acid groups, phosphoric acid groups, etc.), sulfonic acid groups, carboxylic acid groups, and alcoholic hydroxyl groups. Examples of the skeleton having an ethylenically unsaturated bond include a vinyl skeleton, a (meth) acrylate skeleton, and a (meth) allyl ester skeleton.

（但しR⁵は水素又はメチル基であり、R⁶は水素又は他の置換基を有してもよい炭化水素基である。）により表される（メタ）アクリルアミド単量体と、リン酸源化合物とを反応させ、得られた反応生成物を加水分解してなる組成物が好ましい。 (i) Phosphoric acid residue-containing (meth) acrylamide derivative The phosphoric acid residue-containing (meth) acrylamide derivative is represented by the following formula (4):

(Wherein R ⁵ is hydrogen or a methyl group, and R ⁶ is hydrogen or a hydrocarbon group which may have other substituents) and a phosphoric acid source A composition obtained by reacting a compound and hydrolyzing the obtained reaction product is preferable.

R ⁵ of the (meth) acrylamide monomer represented by the formula (4) is preferably a hydrogen group from the viewpoint of good polymerizability. R ⁶ is preferably a hydrogen group from the viewpoint of improving the phosphorus acid residue density when a polymer is prepared. When R ⁶ is a hydrocarbon group, for example, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, 2-methylbutyl group, 3- Examples thereof include alkyl groups such as methylbutyl group, n-octyl group and 2-ethylhexyl group; cycloalkyl groups such as cyclopropyl group and cyclohexyl group; aryl groups such as phenyl group and the like. These groups may have other substituents. Examples of other substituents include sulfonic acid groups that may form a complex salt; N, N-dimethylamino group, N, N-diethylamino An amino group such as a group can be exemplified. Among them, the hydrocarbon group preferably has a sulfonic acid group that may form a complex salt from the viewpoint of improving the acid group density when a polymer is prepared.

（ただしR⁵は式(4)と同じであり、R⁷及びR⁸は水素又は炭素数１〜３のアルキル基であり、R⁹は炭素数１〜３のアルキレン基であり、Mは水素、金属又は３級アミン残基を表す。）により表されるアクリルアミドアルカンスルホン酸塩からなる群から選ばれた少なくとも一種が好ましい。上記式(5)により表されるアクリルアミドアルカンスルホン酸塩としてはターシャリーブチルアクリルアミドスルホン酸が好ましい。 Specific examples of the (meth) acrylamide monomer represented by the formula (4) include acrylamide, methacrylamide, and the following formula (5):

(However, R ⁵ is the same as in formula (4), R ⁷ and R ⁸ are hydrogen or an alkyl group having 1 to 3 carbon atoms, R ⁹ is an alkylene group having 1 to 3 carbon atoms, and M is hydrogen. , Represents a metal or tertiary amine residue.) And is preferably at least one selected from the group consisting of acrylamide alkane sulfonates. As the acrylamide alkane sulfonate represented by the above formula (5), tertiary butyl acrylamide sulfonic acid is preferable.

  The phosphoric acid residue-containing (meth) acrylamide derivative composition is obtained by reacting the (meth) acrylamide monomer as described above with a phosphoric acid source compound and hydrolyzing the resulting reaction product. . As the phosphoric acid source compound, phosphoric anhydride is preferable. The mixing ratio of the (meth) acrylamide monomer and phosphoric anhydride is such that the ratio represented by the formula [(number of moles of phosphoric anhydride) / (number of moles of (meth) acrylamide monomer)] is 0.05 to 1.2. Is preferably in the range of 0.4 to 1.1.

（但しR⁵は水素又はメチル基であり、R⁶は水素又は他の置換基を有してもよい炭化水素基である。）に示すように（メタ）アクリルアミド単量体に対する無水リン酸のモル比が0.5となるように反応させて、ジアクリルアミド系ピロホスホン酸を生成させ、これに対するモル比が無水リン酸と同じ0.5の水で加水分解することにより製造できる。このため（メタ）アクリルアミド単量体に対する無水リン酸のモル比は、0.4〜0.8の範囲であるのが好ましく、0.5〜0.6の範囲であるのがより好ましく、0.52〜0.58の範囲であるのが特に好ましい。また十分に加水分解させるために、水は上記化学量論に基づくモル比よりも10％程度過剰に添加するのが好ましい。 When a phosphoric acid residue-containing (meth) acrylamide derivative composition uses phosphoric anhydride as a phosphoric acid source compound, for example, the following formula (6):

(However, R ⁵ is hydrogen or a methyl group, and R ⁶ is hydrogen or a hydrocarbon group which may have other substituents.) As shown in FIG. It can be produced by reacting to a molar ratio of 0.5 to produce diacrylamide-based pyrophosphonic acid and hydrolyzing with water having the same molar ratio as phosphoric anhydride of 0.5. Therefore, the molar ratio of phosphoric anhydride to (meth) acrylamide monomer is preferably in the range of 0.4 to 0.8, more preferably in the range of 0.5 to 0.6, and in the range of 0.52 to 0.58. Particularly preferred. Moreover, in order to fully hydrolyze, it is preferable to add about 10% of water more than the molar ratio based on the said stoichiometry.

（但しR⁵は水素又はメチル基である。）に示すような反応により、（メタ）アクリルアミドジホスホン酸が生成する。従って、（メタ）アクリルアミド単量体としてアクリルアミド及び／又はメタクリルアミドを用いて（メタ）アクリルアミドホスホン酸を主に製造するには、（メタ）アクリルアミドに対する無水リン酸のモル比［（無水リン酸のモル数）／（（メタ）アクリルアミドのモル数）］が0.4〜0.8の範囲であるのが好ましく、0.5〜0.6の範囲であるのがより好ましく、0.52〜0.58の範囲であるのが特に好ましい。また（メタ）アクリルアミド単量体としてアクリルアミド及び／又はメタクリルアミドを用いて（メタ）アクリルアミドジホスホン酸を主に製造するには、（メタ）アクリルアミドに対する無水リン酸のモル比［（無水リン酸のモル数）／（（メタ）アクリルアミドのモル数）］が１〜1.2の範囲であるのが好ましく、1〜1.15の範囲であるのがより好ましく、1.05〜1.1の範囲であるのが特に好ましい。さらに（メタ）アクリルアミドジホスホン酸を主に製造する場合は、加水分解に際し、（メタ）アクリルアミドと無水リン酸の付加体に対するモル比が１の水を添加することを基本とする。但し十分に加水分解させるために、水は上記化学量論に基づくモル比よりも10％程度過剰に添加するのが好ましい。 When acrylamide and / or methacrylamide is used as the (meth) acrylamide monomer and phosphoric anhydride is used as the phosphoric acid source compound, not only the (meth) acrylamide phosphonic acid obtained according to the formula (6) but also the following formula (7):

(Meth) acrylamide diphosphonic acid is produced by a reaction as shown in (wherein R ⁵ is hydrogen or a methyl group). Therefore, in order to mainly produce (meth) acrylamide phosphonic acid using acrylamide and / or methacrylamide as the (meth) acrylamide monomer, the molar ratio of phosphoric anhydride to (meth) acrylamide [(phosphoric anhydride Number of moles) / (number of moles of (meth) acrylamide)] is preferably in the range of 0.4 to 0.8, more preferably in the range of 0.5 to 0.6, and particularly preferably in the range of 0.52 to 0.58. In order to mainly produce (meth) acrylamide diphosphonic acid using acrylamide and / or methacrylamide as the (meth) acrylamide monomer, the molar ratio of phosphoric anhydride to (meth) acrylamide [(phosphoric anhydride The number of moles) / (number of moles of (meth) acrylamide)] is preferably in the range of 1 to 1.2, more preferably in the range of 1 to 1.15, and particularly preferably in the range of 1.05 to 1.1. Further, in the case of mainly producing (meth) acrylamide diphosphonic acid, water having a molar ratio of 1 to the adduct of (meth) acrylamide and phosphoric anhydride is basically added during the hydrolysis. However, in order to sufficiently hydrolyze, it is preferable to add water by about 10% more than the molar ratio based on the above stoichiometry.

（但しR⁵は水素又はメチル基であり、R⁶は水素又は他の置換基を有してもよい炭化水素基であり、jは１又は２である。）により表されるジアクリルアミドポリリン酸ホスホン酸も生成すると推測される。リン系酸残基含有（メタ）アクリルアミド誘導体組成物は、ジアクリルアミドポリリン酸ホスホン酸の加水分解により生成する下記式(9)：

（但しR⁵は水素又はメチル基であり、R⁶は水素又は他の置換基を有してもよい炭化水素基であり、kは１又は２である。）により表される２リン酸残基又は３リン酸残基を有する単量体を含んでもよい。 When the molar ratio of phosphoric anhydride to (meth) acrylamide monomer is more than 0.5, in the stage before hydrolysis, the following formula (8):

(Wherein R ⁵ is hydrogen or a methyl group, R ⁶ is hydrogen or a hydrocarbon group which may have other substituents, and j is 1 or 2). It is speculated that phosphonic acid is also produced. The phosphoric acid residue-containing (meth) acrylamide derivative composition is produced by hydrolysis of diacrylamide polyphosphoric acid phosphonic acid:

(Wherein R ⁵ is hydrogen or a methyl group, R ⁶ is hydrogen or a hydrocarbon group which may have other substituents, and k is 1 or 2). A monomer having a group or a triphosphate residue may be included.

  The reaction procedure when phosphoric anhydride is used as the phosphoric acid source compound will be described. First, a solution consisting of [(meth) acrylamide monomer + solvent] is put into a reactor equipped with a stirrer and a reflux condenser, and the temperature is raised to 50 to 75 ° C. At this time, it is preferable to add a known polymerization inhibitor such as hydroquinone monomethyl ether and paramethoxyhydroquinone together. After reaching the predetermined temperature, phosphoric anhydride is added. Phosphoric anhydride is preferably added in portions over 2 to 10 times within 1 to 7 hours. This promotes the formation reaction of the phosphonic acid group-containing acrylamide monomer and improves the yield. However, it is not intended to be limited to the divided addition, and may be added in small portions continuously as necessary. Addition of phosphoric anhydride generates heat, and the reaction temperature usually rises to about 70 to 90 ° C. Thereafter, the reaction is kept at 50 to 110 ° C. and the reaction is continued for 1 to 3 hours. The resulting reaction solution is cooled to room temperature. When unreacted phosphoric anhydride, by-product inorganic polyphosphoric acid, or the like is precipitated by cooling, the solid precipitated by suction filtration is separated by filtration.

  Next, water is added to the reaction solution to generate heat, but it is hydrolyzed by maintaining the temperature at 60 to 100 ° C. for 15 minutes to 1 hour.

  As the solvent, a solvent containing no active hydrogen and / or an acidic solvent is preferable. Examples of the solvent not containing active hydrogen include amide solvents such as N, N-dialkyl (meth) acrylamide, dimethylformamide (DMF), N, N-dimethylacetamide (DMAc), and sulfoxides such as dimethyl sulfoxide (DMSO). A solvent is mentioned. Examples of the acidic solvent include organic acid solvents such as alkyl carboxylic acids and alkyl phosphoric acids. As these solvents, a single substance may be used, or a mixture of two or more kinds may be used.

  Among them, the solvent is preferably at least one selected from the group consisting of N, N-dialkyl (meth) acrylamide, dimethylformamide, N, N-dimethylacetamide and dimethyl sulfoxide. Among them, N, N-dimethylacrylamide (DMAA) has excellent solubility in (meth) acrylamide monomers, phosphoric acid source compounds and phosphorus acid residue-containing (meth) acrylamide derivative compositions, and has a boiling point of 171 to Since it is 172 ° C., the reaction temperature selection range is wide, and there are advantages that a side reaction can be sufficiently prevented if a polymerization inhibitor is used in combination.

  In order to accelerate the reaction and suppress the formation of by-products, the reaction solution preferably has an initial concentration [concentration of (meth) acrylamide monomer raw material] before addition of phosphoric anhydride of 20 to 70% by mass. 25 to 60% by mass is more preferable.

  When the phosphoric acid residue-containing (meth) acrylamide derivative composition is isolated after the reaction, the viscous solution is deposited by filtering the reaction solution into a poor solvent little by little. As the poor solvent, a nonpolar solvent is preferable, and examples thereof include acetone, tetrahydrofuran (THF), dioxane, benzene, toluene, xylene, ether and the like. The nonpolar solvent preferably has a low specific gravity and a relatively low boiling point. The poor solvent is used in a large excess amount of 5 to 15 times the volume of the reaction product. What is necessary is just to repeat washing | cleaning operation of the viscous liquid by a poor solvent as needed. The isolated phosphorus acid residue-containing (meth) acrylamide derivative composition is dried. The drying method is preferably a method of vacuum treatment at room temperature to 100 ° C., a method of heat treatment at 60 to 100 ° C. for 1 to 4 hours using a hot air oven or the like.

（但しR⁵は水素又はメチル基であり、R⁶は水素又は置換もしくは無置換のアルキル基であり、xは０〜２の整数を表す。）により表されるホスホン酸基含有（メタ）アクリルアミド単量体を含むのが好ましい。 The phosphoric acid residue-containing (meth) acrylamide derivative composition thus obtained has the following formula (10):

(Wherein R ⁵ is hydrogen or a methyl group, R ⁶ is hydrogen or a substituted or unsubstituted alkyl group, and x represents an integer of 0 to 2). Preferably it contains a monomer.

（但しR⁵は水素又はメチル基であり、R⁶は水素又は置換もしくは無置換のアルキル基である。）により表されるホスホン酸基含有（メタ）アクリルアミド単量体、及び／又は下記式(12)：

（但しR⁵は水素又はメチル基である。）により表されるジホスホン酸基含有（メタ）アクリルアミド単量体を含むのがより好ましい。重合体を調製した時のホスホン酸基密度を高くする観点から、式(11)により表されるホスホン酸基含有（メタ）アクリルアミド単量体、及び式(12)により表されるジホスホン酸基含有（メタ）アクリルアミド単量体の合計含有率は、リン系酸残基含有（メタ）アクリルアミド誘導体組成物全体を100質量％として、５質量％以上であるのが好ましく、30質量％以上であるのがより好ましく、50質量％以上であるのが特に好ましい。 The phosphoric acid residue-containing (meth) acrylamide derivative composition has the following formula (11):

(Wherein R ⁵ is hydrogen or a methyl group, and R ⁶ is hydrogen or a substituted or unsubstituted alkyl group), and / or a phosphonic acid group-containing (meth) acrylamide monomer and / or the following formula ( 12):

It is more preferable that the diphosphonic acid group-containing (meth) acrylamide monomer represented by (wherein R ⁵ is hydrogen or a methyl group). From the viewpoint of increasing the phosphonic acid group density when preparing the polymer, the phosphonic acid group-containing (meth) acrylamide monomer represented by formula (11) and the diphosphonic acid group represented by formula (12) The total content of the (meth) acrylamide monomer is preferably 5% by mass or more and 100% by mass or more, based on 100% by mass of the phosphoric acid residue-containing (meth) acrylamide derivative composition as a whole. Is more preferably 50% by mass or more.

  The phosphorus acid residue-containing (meth) acrylamide derivative composition may contain unreacted (meth) acrylamide monomer and / or by-product (meth) acrylonitrile.

（ただしR¹⁰は水素又はアルキル基であり、R¹¹は水素又は置換もしくは無置換のアルキル基であり、pは１〜６の整数である。）により表されるリン酸基含有不飽和単量体（以下「単量体(I)」と呼ぶ）が特に好ましい。R¹⁰はH又はCH₃であり、R¹¹はH、CH₃又はCH₂Clであるのが好ましい。 (ii) Phosphoric group-containing unsaturated monomer As an exemplary compound of an unsaturated monomer containing a phosphoric acid group, the following general formula (13):

(Wherein R ¹⁰ is hydrogen or an alkyl group, R ¹¹ is hydrogen or a substituted or unsubstituted alkyl group, and p is an integer of 1 to 6). (Hereinafter referred to as “monomer (I)”) is particularly preferred. R ¹⁰ is preferably H or CH ₃ and R ¹¹ is preferably H, CH ₃ or CH ₂ Cl.

  The structural formulas and physical properties of typical monomers (I) are shown in Tables 1 and 2, respectively. These monomers are sold by Unichemical Corporation under the trade name Phosmer (registered trademark). However, the phosphate group-containing unsaturated monomer that can be used in the present invention is not limited to these.

The phosphate residue of monomer (I) may be dissociated or may form a complex salt. When forming a complex salt, in order to neutralize the charge, for example, ammonium ions containing mono-, di- or tri-alkyl groups such as primary, secondary, tertiary or quaternary alkyl groups, allyl groups, aralkyl groups, etc. preferably forms an alkanolamine residue and complex, especially _{^{N + R 12 4-f (}} OH) f ( where R ¹² is an alkyl group having 1 to 18 carbon atoms, an aromatic group having 6 to 12 carbon atoms and carbon It represents at least one selected from the group consisting of alicyclic groups of formula 6 to 12, and f represents a positive integer of 1 to 3).

（ただしR¹⁰及びR^10'はそれぞれ独立に水素基又はメチル基であり、R¹¹及びR^11'はそれぞれ独立に水素基又は置換もしくは無置換のアルキル基であり、p'及びp''はそれぞれ独立に１〜６の整数である。）により表されるリン酸基含有ジエステル不飽和単量体（以下「単量体(II)」と呼ぶ）、及び／又は下記一般式(15):

（ただしR¹⁰及びR^10'はそれぞれ独立に水素基又はメチル基であり、R¹¹及びR^11'はそれぞれ独立に水素基又は置換もしくは無置換のアルキル基であり、p'及びp''はそれぞれ独立に１〜６の整数である。）により表されるピロリン酸基含有不飽和単量体（以下「単量体(III)」と呼ぶ）を用いてもよい。 As the phosphate group-containing unsaturated monomer, the following general formula (14):

(However, R ¹⁰ and R ^{10 ′} are each independently a hydrogen group or a methyl group, R ¹¹ and R ^{11 ′} are each independently a hydrogen group or a substituted or unsubstituted alkyl group, and p ′ and p ″ are Each independently an integer of 1 to 6.) A phosphate group-containing diester unsaturated monomer (hereinafter referred to as “monomer (II)”) and / or the following general formula (15):

(However, R ¹⁰ and R ^{10 ′} are each independently a hydrogen group or a methyl group, R ¹¹ and R ^{11 ′} are each independently a hydrogen group or a substituted or unsubstituted alkyl group, and p ′ and p ″ are A pyrophosphate group-containing unsaturated monomer (hereinafter referred to as “monomer (III)”) represented by the following formulas may be used.

（ただしR¹⁰及びR^10'はそれぞれ独立に水素基又はメチル基である。）により表されるジ［（メタ）クリロイルオキシエチル］ホスフェートが好ましい。 As the monomer (II), the following formula (16):

Di [(meth) acryloyloxyethyl] phosphate represented by (wherein R ¹⁰ and R ^{10 ′} are each independently a hydrogen group or a methyl group) is preferred.

により表されるジ（メタクリロイルオキシエチル）アシッド・ピロホスフェートが好ましい。 As the monomer (III), the following formula (17);

Di (methacryloyloxyethyl) acid pyrophosphate represented by is preferred.

  Monomers (II) and (III) may be used alone, or monomer (I) and monomer (II) and / or monomer (III) may be used in combination.

(iii) Unsaturated monomer containing sulfonic acid group As the unsaturated monomer containing a sulfonic acid group, the above-mentioned tertiary butyl acrylamide sulfonic acid, allyl sulfonic acid, methallyl sulfonic acid (methallyl sulfonic acid) acid), vinyl sulfonic acid, p-styrene sulfonic acid, (meth) acrylic acid butyl-4-sulfonic acid, (meth) acrylooxybenzene sulfonic acid, and the like.

(iv) Carboxylic acid group-containing unsaturated monomer Examples of unsaturated monomer containing a carboxylic acid group include (meth) acrylic acid, crotonic acid, maleic acid, fumaric acid, itaconic acid, maleic anhydride Thing etc. are mentioned.

(v) Unsaturated monomer containing alcoholic hydroxyl group Unsaturated monomer containing alcoholic hydroxyl group includes glycerol dimethacrylate [for example, “Blemmer GMR”, “GMR-R”, “GMR-H”. Glycerol di (meth) acrylates such as “Nippon Yushi Co., Ltd.”, etc.], glycerol methacrylate acrylate [for example, “Blemmer GAM”, “Same GAM-R” (Nippon Yushi Co., Ltd.) etc .; 1,6-hexanediol diglycidyl ether acrylate [eg, trade name “NK Oligo EA-5521” (manufactured by Shin-Nakamura Chemical Co., Ltd.)]; 1,4-butanediol diglycidyl ether acrylate [eg, trade name “NK Oligo EA-5520 "(manufactured by Shin-Nakamura Chemical Co., Ltd.) etc.]; bisphenol A type epoxy acrylate [for example, trade name" NK Oligo EA-1020 "(manufactured by Shin-Nakamura Chemical Co., Ltd.)] Sa methylene di (meth) acrylate; 2-hydroxymethyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate such as 2-hydroxyethyl (meth) acrylate.

  Among them, glycerol di (meth) acrylate, 1,6-hexanediol diglycidyl ether acrylate, 1,4-butanediol diglycidyl ether acrylate, bisphenol A type epoxy acrylate and hexamethylenediol diacrylate have ethylenically unsaturated groups. Since it has two in a molecule | numerator, it is preferable to use when preparing a solid polymer electrolyte membrane by photopolymerization or radiation polymerization.

（ただしR¹³及びR^13'はそれぞれ独立に水素基又はメチル基である。）により表される化合物が好ましい。 These alcoholic hydroxyl group-containing unsaturated monomers are further improved in compatibility with the phosphate esterified unsaturated alcohol copolymer by phosphoric acid monoesterification of these hydroxyl groups. In particular, an alcoholic hydroxyl group-containing unsaturated monomer phosphoric acid monoesterified monomer having two ethylenically unsaturated groups in the molecule has good crosslinking efficiency when photopolymerized. Among such phosphoric acid ester products, a compound obtained by phosphorylating glycerol di (meth) acrylate, that is, the following formula (18):

A compound represented by (wherein R ¹³ and R ^{13 ′} are each independently a hydrogen group or a methyl group) is preferred.

The method of phosphoric esterifying the alcoholic hydroxyl group-containing unsaturated monomer may be the same as the phosphoric esterification method of the unsaturated alcohol copolymer. However, not only hydrogen peroxide solution but also water alone may be used for hydrolysis. The water is not necessarily added at the same time P ₂ O _5, was added the total amount of P ₂ O _5, may be hydrolyzed.

  The unsaturated monomers (i) to (v) may be used alone or in combination of two or more. Among them, it is preferable to use the (i) phosphorus acid residue-containing (meth) acrylamide derivative having a high acidic group density of the polymer.

(A-2) Unsaturated monomer and oligomer not containing an acidic group Unsaturated monomer and oligomer each not containing an acidic group include molecules other than those described in (A-1), which are not gases at normal temperatures. Of these, all unsaturated monomers and oligomers having one or more ethylenically unsaturated bonds are targeted, but among them (meth) acrylonitrile, conjugated diene liquid oligomers or hydrides thereof, alkylamino group-containing unsaturated monomers. Containing multiple ethylenically unsaturated bonds in the molecule, (meth) acrylates, styrenes (eg, substituted and unsubstituted styrenes), vinyls (eg, vinyl chloride, vinyl acetate, etc.) And at least one selected from the group consisting of a monomer comprising an unsaturated monomer, a fluorine group-containing unsaturated monomer, and a vinyl aromatic-conjugated diene copolymer.

（但しR¹⁴及びR¹⁵はそれぞれ独立に(a) エチレン性不飽和結合を１個以上有し、かつ他の原子団を有してもよい炭化水素基、(b) エチレン性不飽和結合を有さず、かつ他の原子団を有してもよい炭化水素基又は(c) 水素基であり、かつR¹⁴及びR¹⁵の少なくとも一方は前記(a) エチレン性不飽和結合を有する炭化水素基であり、R¹⁶及びR¹⁷はそれぞれ独立に水素基又はメチル基であり、かつR¹⁶及びR¹⁷の少なくとも一方は水素基であり、tは重合度を表す。）により表されるものがさらに好ましい。ただし共役ジエン系液状オリゴマーとして、式(19)に示すような重合体鎖中の共役ジエン単位が1, 2−結合であるものに限定する趣旨ではなく、共役ジエン単位が1, 4−結合であるものであってもよい。 (i) Conjugated diene-based liquid oligomer and hydride thereof As the conjugated diene-based liquid oligomer, those having at least two ethylenically unsaturated bonds in the molecule are preferable, and the group consisting of butadiene oligomer, isoprene oligomer and derivatives thereof More preferred is at least one selected from The conjugated diene-based liquid oligomer has the following general formula (19):

(However, R ¹⁴ and R ¹⁵ are each independently (a) a hydrocarbon group which has one or more ethylenically unsaturated bonds and may have other atomic groups, and (b) an ethylenically unsaturated bond. A hydrocarbon group which does not have and may have another atomic group or (c) a hydrogen group, and at least one of R ¹⁴ and R ¹⁵ has (a) a hydrocarbon having an ethylenically unsaturated bond R ¹⁶ and R ¹⁷ are each independently a hydrogen group or a methyl group, and at least one of R ¹⁶ and R ¹⁷ is a hydrogen group, and t represents the degree of polymerization). Further preferred. However, the conjugated diene-based liquid oligomer is not limited to those in which the conjugated diene unit in the polymer chain is a 1,2-bond as shown in the formula (19), but the conjugated diene unit is a 1,4-bond. There may be something.

R ¹⁴ and R ¹⁵ are each independently (a) a hydrocarbon group which has one or more ethylenically unsaturated bonds and may have other atomic groups, and (b) has an ethylenically unsaturated bond. And at least one of R ¹⁴ and R ¹⁵ is (a) a hydrocarbon group having an ethylenically unsaturated bond. As long as there is no particular limitation. Examples of other atomic groups that R ¹⁴ and R ¹⁵ may have include at least one selected from the group consisting of urethane bonds, ester bonds, ether bonds, isocyanate groups, hydroxyl groups, carboxyl groups, and alkoxy groups. Specific examples of R ¹⁴ and R ¹⁵ include a (meth) acryl group.

Although there is no restriction | limiting in particular in the molecular weight of a conjugated diene type liquid oligomer, A thing with a number average molecular weight of 500-50,000 is preferable. Among the conjugated diene-based liquid oligomers represented by the formula (19), those in which R ¹⁶ and R ¹⁷ are both hydrogen groups are commercially available products such as “NISSO-PB TEA-1000”, “NISSO-PB TE-2000” ( (Nippon Soda Co., Ltd.).

  The conjugated diene-based liquid oligomer may contain other conjugated diene as a polymerization component, if necessary. When the conjugated diene-based liquid oligomer is a butadiene oligomer or a derivative thereof, isoprene may be included as a copolymerization component. When the conjugated diene liquid oligomer is an isoprene oligomer or a derivative thereof, butadiene may be included as a copolymerization component. Other conjugated dienes include 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 2-methyl-1,3-pentadiene, 1,3-hexadiene, 4,5-diethyl-1 , 3-octadiene, 3-butyl-1,3-octadiene, chloroprene and the like.

  The conjugated diene-based liquid oligomer may be a copolymer with an olefin. When the conjugated diene-based liquid oligomer is a copolymer of a conjugated diene and an olefin, any of a random copolymer, a block copolymer, and a graft copolymer may be used.

（但しR¹⁴〜R¹⁷及びtは式(19)と同じである。）により表されるものが好ましい。式(20)により表される水素化共役ジエン系液状オリゴマーの市販品として、例えば「NISSO-PB TEAI-1000」（日本曹達（株）製）等がある。 The conjugated diene liquid oligomer may be hydrogenated. The hydrogenated conjugated diene-based liquid oligomer has the following general formula (20):

(Wherein R ^{14 to} R ¹⁷ and t are the same as those in formula (19)) are preferred. Examples of commercially available hydrogenated conjugated diene liquid oligomers represented by the formula (20) include “NISSO-PB TEAI-1000” (manufactured by Nippon Soda Co., Ltd.).

(ii) Alkylamino group-containing unsaturated monomer Examples of the unsaturated monomer containing an alkylamino group include the N, N-dialkyl (meth) acrylamide, dimethylaminoethyl (meth) acrylate, and diethylaminoethyl (meth) acrylate. , Dimethylaminopropyl (meth) acrylate, dimethylaminobutyl (meth) acrylate, dipropylaminoethyl (meth) acrylate, dibutylaminoethyl (meth) acrylate, dimethylaminoethyl (meth) acrylamide, diethylaminoethyl (meth) acrylamide, dimethyl Examples include aminopropyl (meth) acrylamide, dimethylaminobutyl (meth) acrylamide, dipropylaminoethyl (meth) acrylamide, and dibutylaminoethyl (meth) acrylamide. .

(iii) (Meth) acrylic acid esters Examples of (meth) acrylic acid esters include methyl (meth) acrylate, ethyl (meth) acrylate, and alkyl (meth) acrylate.

(iv) Monomers containing a plurality of ethylenically unsaturated bonds in the molecule As monomers containing a plurality of ethylenically unsaturated bonds in the molecule, for example, diisocyanate and glycerol di (meth) acrylate are used. Urethane acrylate obtained by reaction [for example, “NK Oligo U-4HA” (made by Shin-Nakamura Chemical Co., Ltd.)], ethylene glycol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, divinylbenzene, etc. Is mentioned.

(v) Fluorine group-containing unsaturated monomer As the fluorine group-containing unsaturated monomer, for example, hydrofluoroalkyl group-containing (meth) acrylic acid esters such as perfluorooctylethyl (meth) acrylate; perfluoroalkyl group-containing (Meth) acrylic acid esters; perfluoroalkyl group-containing vinyls such as perfluorobutylethylene, perfluorohexylethylene, perfluorooctylethylene, perfluorodecylethylene; hydrofluoroalkyl group-containing vinyls, and the like.

(vi) Vinyl aromatic-conjugated diene copolymer The vinyl aromatic-conjugated diene copolymer is composed of a copolymer having at least a vinyl aromatic unit and a conjugated diene unit. Styrene is preferred as the vinyl aromatic component. Isoprene is preferred as the conjugated diene component. The ratio of the vinyl aromatic component and the conjugated diene component in the vinyl aromatic-conjugated diene copolymer is not particularly limited, and it has physical properties such as toughness, flexibility, and mechanical strength required for the solid polymer electrolyte membrane. What is necessary is just to set suitably according to.

  The vinyl aromatic-conjugated diene copolymer may be a derivative modified by a treatment such as introduction of a functional group or other atomic group or hydrogenation. Examples of the functional group include a (meth) acryl group, an isocyanate group, a hydroxyl group, a carboxyl group, an alkoxy group, a sulfonic acid group, an epoxy group, and a hydrocarbon group. Examples of other atomic groups include a urethane bond, an ester bond, and an ether bond. Examples of commercially available vinyl aromatic-conjugated diene copolymers include “Claprene LIR-310” (manufactured by Kuraray Co., Ltd.).

  The oligomer (i) and the unsaturated monomers (ii) to (vi) may be used alone or in combination. Of these, the conjugated diene liquid oligomer (i) is preferred. When other conductive resin contains the conjugated diene liquid oligomer component together with the acidic group-containing unsaturated monomer component, the phosphate esterified unsaturated alcohol copolymer also acts as a dispersant.

  The mass ratio between the unsaturated monomer (A-1) containing an acidic group and the unsaturated monomer or oligomer (A-2) containing no acidic group is an acidic group that has a positive effect on proton conductivity. [Acid group-containing unsaturated monomer (A-1)] / [Unsaturated monomer or oligomer containing no acid group (A-1) so that the unsaturated monomer (A-1) is dominant -2)] = 100/0 to 50/50 is preferable.

(B) Non-conductive resin Non-conductive resins include melamine resin (for example, trimethoxymethyl melamine resin), vinyl hydrophilic polymer (for example, polyvinyl alcohol), poly (meth) acrylonitrile, poly (meth) acrylic. Acid esters, polyacrylamides, poly (meth) acrylic acid, polyacetal, water-soluble urethane resin, cellulose and modified products thereof, polystyrenes, polyvinyl chloride, polyvinyl acetate, conjugated diene-based liquid oligomers or hydrides thereof At least selected from the group consisting of a polymer, a polymer of the alkylamino group-containing unsaturated monomer, a polymer of the fluorine group-containing unsaturated monomer, and the vinyl aromatic-conjugated diene copolymer. It is preferable to add one kind. By adding such a non-conductive resin, the film forming property, water resistance, chemical resistance, flexibility and the like of the solid polymer electrolyte membrane are further improved. You may use together said other conductive resin and nonelectroconductive resin.

(C) Mixing ratio The mixing ratio of the phosphate esterified unsaturated alcohol copolymer and other resin (other conductive resin and / or non-conductive resin) is not particularly limited, and is appropriately determined according to the desired physical properties. The ratio based on the weight of solid content [(phosphate esterified unsaturated alcohol copolymer) / (other resin)] is preferably in the range of 99/1 to 1/99. In particular, it is more preferably in the range of 95/5 to 40/60, and particularly preferably in the range of 95/5 to 60/40 in which the phosphate esterified unsaturated alcohol copolymer is the main component. In addition, among other resins, the mass ratio of conductive resin to non-conductive resin is such that conductive resin / non-conductive resin = 100 / A range of 0 to 50/50 is preferable. When the phosphate esterified unsaturated alcohol copolymer is used as a dispersant for a solid polymer electrolyte membrane containing the acidic group-containing unsaturated monomer component and the conjugated diene-based liquid oligomer component, the solid content is on a weight basis. If the ratio [(phosphate esterified unsaturated alcohol copolymer) / (other resin)] is 1/99 or more, a sufficient effect can be obtained.

(D) Production method The second solid polymer electrolyte membrane comprises: (i) a phosphate esterified unsaturated alcohol copolymer, the other resin (other conductive resin and / or non-conductive resin) and solvent (Ii) Phosphate esterified unsaturated alcohol copolymer and other resins (other conductive materials) A mixture containing an unsaturated monomer constituting a conductive resin and / or a non-conductive resin) can be produced by a polymerization method in which the mixture is treated with light, radiation or heat.

(i) Casting method In the case of the casting method, commercially available products can be used as other resins. Moreover, you may prepare another resin by superposing | polymerizing the above unsaturated monomers which can comprise another resin as needed by well-known methods, such as solution polymerization. The solvent may be appropriately selected according to the phosphate esterified unsaturated alcohol copolymer and other resins, and examples thereof include DMF, THF, lower alcohols and the like. The resin solid content concentration, heating temperature, and film thickness of the polymer solution may be the same as in the case of the first solid polymer electrolyte membrane. Similarly to the case of the first solid polymer electrolyte membrane, the mechanical strength can be increased by further stretching the cast film thus formed. Stretching preferably involves heating.

(ii) Polymerization Method A method for producing the second solid polymer electrolyte membrane by photopolymerization will be described below. A method for producing a film by photopolymerization is a composition containing a mixture containing a phosphate esterified unsaturated alcohol copolymer and an unsaturated monomer constituting the other resin and a photosensitizer (hereinafter referred to as “photosensitizer”). Unless otherwise specified, it is called “unsaturated composition”), cast on a plate covered with a material (fluorine polymer, etc.) to which it does not adhere, covered with a UV transparent plate, and then irradiated with UV rays. To do. After the unsaturated composition is impregnated in or applied to the reinforcing material, the reinforcing material may be sandwiched between UV transmissive support substrates, and the unsaturated composition may be photopolymerized by irradiating ultraviolet rays to form a composite film. . The polymerization initiator that can be used and the amount thereof used, the material of the support substrate, the ultraviolet irradiation intensity, the reinforcing material and the like may be the same as those described in, for example, JP-A-2003-86021.

  In order to impart the peelability of the polymer obtained by ultraviolet polymerization from the support substrate, a release agent may be mixed in advance with the unsaturated composition. As the release agent, those having relatively good compatibility with the unsaturated composition are preferable. The release agent is preferably a fluorine-based surfactant, and more preferably a fluorine-based alcohol. Specific examples of the release agent include perfluorooctylethanol, perfluorooctylsulfoamidoethanol and ethylene oxide adducts thereof; hydrocarbon surfactants; polymer polyoxyethylene glycol (eg, carbowax). The addition amount of the fluorine-based release agent is in the range of 0.1 to 5% by mass, preferably in the range of 0.2 to 1% by mass, with respect to the total mass of the unsaturated composition. If this added amount is less than 0.1% by mass, the peelability is insufficient. On the other hand, even if the added amount exceeds 5% by mass, the peeling effect is saturated.

  The thickness of the photopolymerized film is also usually about 20 to 500 μm, preferably about 20 to 200 μm. The mechanical strength can be increased by further heating the photopolymerized film. The second solid polymer electrolyte membrane of the present invention thus obtained has a uniform composition.

[3] Fuel cell The solid polymer electrolyte membrane of the present invention has excellent proton conductivity of 10 ⁻⁴ to 10 ⁻² S · cm ⁻¹ , and the proton conductivity is small in temperature dependence. It is suitable as an electrolyte membrane.

  The structure of the fuel cell may be a known one. Usually, a fuel cell can be formed by laminating a plurality of unit fuel cells (membrane / electrode assemblies) via separators. The unit fuel cell is composed of an anode and a cathode electrode and an electrolyte membrane. The electrode includes a gas diffusion layer (porous carbon-based material or the like) and a catalyst layer (platinum particles or the like), and catalyst particles are coated on the gas diffusion layer to form a catalyst layer. A unit fuel cell is configured by joining an anode electrode and a cathode electrode so that the catalyst layers are opposed to both sides of the electrolyte membrane.

  The separator separates fuel gas (hydrogen, methane, etc.) and oxidant gas (oxygen or air), secures a flow path for the fuel gas and oxidant gas, and further generates electricity generated by the fuel cell. It plays a role of transmitting information to the outside. Accordingly, the separator is made of a conductive material such as a carbon material, a carbon composite material (such as a composite material of carbon and a thermosetting resin or a thermoplastic resin), a metal material, or a metal composite material (such as a composite material of a metal and carbon). It is formed. Further, a groove (reactive gas flow path) that forms a flow path for the fuel gas and the oxidant gas is formed on the surface of the separator at the contact portion with the electrode.

  The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples.

Example 1
375 g of THF was placed in an automatic synthesis reactor (internal volume 1 L, manufactured by Unichemical Co., Ltd.) connected to a reflux condenser, a powder inlet and a thermometer, and 173 g of polyvinyl alcohol containing vinyl acetate units (trade name) “Kuraray LM Polymer LM-20”, saponification rate: 38 to 42 mol%, hydroxyl group equivalent: about 173, manufactured by Kuraray Co., Ltd.) was added and dissolved. While maintaining the stirring speed at 2,120 rpm and maintaining the reaction temperature in the range of 30-58 ° C., 18 g of 7% by mass hydrogen peroxide (total of hydrogen peroxide and water: 0.94 mol) and 78 g P ₂ O ₅ (0.55 mol) was added in 6 times, approximately 1/6 each, over 6 hours at approximately equal intervals. After all the water and P ₂ O ₅ had been added, an aging reaction was performed for 4 hours under a temperature condition of 30 ° C. and a stirring condition of 2,120 rpm.

  The solution (reaction product) containing the obtained phosphate esterified unsaturated alcohol copolymer (hereinafter referred to as “polymer A” unless otherwise specified) is filtered through a wire mesh (100 mesh), Impurities such as gelled products were removed. An equal volume of n-hexane was added to the reaction product after filtration, and the resulting viscous resin was filtered. In the filtrate, THF containing normal phosphoric acid in which unreacted phosphoric anhydride was changed was dissolved and became cloudy. Polymer A was washed twice more with the same amount of n-hexane. The filtrate when washed for the third time was almost transparent. The purified polymer A was dissolved in THF to prepare a solution of 534 g. A small amount was extracted from the obtained purified polymer A-containing THF solution, dried in a hot air dryer at 100 ° C. for 30 minutes, and the mass was measured. As a result, the solid content in this solution was 42.6% by mass. The dry weight of the polymer A after purification calculated from this concentration was 534 (g) × 0.426 = 227.5 g, and the yield relative to the theoretical yield (253 g) was 90%.

  A small amount was extracted from the purified polymer A-containing THF solution, added to a 30 vol% water / 70 vol% methanol mixed solution, and the resin acid value (using a 1N KOH aqueous solution, the same applies below) was measured. (Theoretical acid value of Kuraray LM polymer LM-20 phosphated ester: 442.7 mg / g). The hue value measured by the Gardner method of the purified polymer A-containing THF solution was 1.

  Purified polymer A-containing THF solution and trimethoxymethylmelamine resin (trade name “Smitex Resin M-3”, manufactured by Sumitomo Chemical Co., Ltd., the same shall apply hereinafter) in a 10% by mass methanol solution in solid content ratio A / trimethoxymethylmelamine was mixed to 71.4 / 28.6 to prepare a polymer solution. The obtained polymer solution was cast into a polypropylene film container (bottom surface: 10 cm × 10 cm), placed in an air circulation dryer, heated from room temperature to 70 ° C. and dried for 24 hours. The produced film was peeled off with a spatula to produce a solid polymer electrolyte membrane having a thickness of 102 μm.

Reference example 1
Polymer A was prepared in the same manner as in Example 1 except that water was used instead of hydrogen peroxide. The obtained crude polymer A was purified in the same manner as in Example 1, and then a 42.6 mass% THF solution was prepared. As a result, the hue value measured by the Gardner method was 3.

  From the above, it is clear that the hue of the resulting phosphate esterified unsaturated alcohol copolymer is improved by using aqueous hydrogen peroxide for the phosphoric esterification of the unsaturated alcohol copolymer. .

Example 2
15 g of the purified polymer A-containing THF solution (42.6% by mass) prepared in Example 1, 4.08 g of triethanolamine, 5.0 g of water, and 30 g of methanol were mixed and stirred at room temperature for 30 minutes. The polymer A was converted to triethanolamine. The pH of the obtained solution was 5.4, and the solid content was 21.5% by mass (measured with an automatic balance at a temperature of 120 ° C., the same applies hereinafter). 6.45 g of trimethoxymethylmelamine resin was added to a solution of the obtained polymer A triethanolamine salt (hereinafter referred to as “polymer AA” unless otherwise specified) to prepare a polymer solution. The obtained polymer solution was cast into a polypropylene film container (bottom surface: 10 cm × 10 cm), placed in an air circulation dryer, heated from room temperature to 50 ° C. and dried for 24 hours. The produced film was peeled off with a spatula, and this was heat-treated at 130 ° C. for 10 minutes with a high-temperature air circulation dryer to produce a solid polymer electrolyte membrane having a thickness of 100 μm.

  The physical properties of the solid polymer electrolyte membranes produced in Examples 1 and 2 were measured by the following methods. The results are shown in Table 3.

(1) Water resistance: A 1 cm long x 4 cm wide strip sample was cut out, and the vertical x horizontal area was measured and used as a reference. This was immersed in water at room temperature, taken out after 30 minutes, the length and width were measured, the length × width area was calculated, and the swelling ratio was determined.
(2) Methanol resistance: A strip sample measuring 1 cm in length x 4 cm in width was cut out and the area in the length and width was measured and used as a reference. This was immersed in methanol at room temperature, taken out after 30 minutes, the length and width were measured, the length and width areas were calculated, and the swelling ratio was obtained.
(3) Hot water resistance: A 1 cm long x 4 cm wide strip sample was cut out and the vertical x horizontal area was measured and used as a reference. This was immersed in hot water at 80 ° C., taken out after 2 hours, the length and width were measured, the length × width area was calculated, and the swelling ratio was obtained.
(4) Surface resistivity: Measured with a surface resistivity meter (SME-8310, manufactured by Toa Denpa Kogyo Co., Ltd.) at 23 ° C / RH 67%.
(5) Proton conductivity: measured using the complex impedance method. A 3 cm × 1 cm rectangular sample was cut out and placed in an open impedance cell. This cell was installed in a constant temperature and humidity chamber, and impedance measurement was performed at a relative humidity of 90% and a measurement temperature range of 35 to 80 ° C. The obtained data was subjected to plane complex impedance analysis, and the conductivity was obtained from the resistance value of the sample obtained by performing the cole-cole plot graphic processing on the result.

Notes: (1) Polyvinyl alcohol containing vinyl acetate units that have been phosphated.
(2) A triethanolamine salt of polyvinyl alcohol containing a vinyl acetate unit containing a phosphate ester.
(3) Sumitex Resin M-3, manufactured by Sumitomo Chemical Co., Ltd.

Comparative Example 1
Using polyvinyl alcohol (trade name “POVAL R-1130”, manufactured by Kuraray Co., Ltd.), in accordance with the method described in Examples of JP-A-6-112010, phosphate esterified polyvinyl alcohol (unless otherwise noted) Is referred to as “polymer VAP”). The acid value of the polymer VAP was measured in the same manner as in Example 1. As a result, it was 530 mg / g (theoretical acid value of phosphoric esterified Poval R-1130: 903). Polymer VAP was dissolved in water to prepare a 10% by mass (solid content concentration) polymer aqueous solution. A film was produced in the same manner as in Example 1 using the obtained aqueous polymer solution. However, the obtained film was highly hygroscopic and it was difficult to maintain the film state at room temperature / normal humidity. Therefore, physical property measurement was impossible.

Example 3
(1) Phosphate esterification of polyvinyl alcohol containing vinyl acetate units
Polymer A was prepared in the same manner as in Example 1 except that 375 g of N, N-dimethylacrylamide (DMAA) was used as a solvent instead of THF. The obtained reaction product solution was filtered through a wire mesh (100 mesh) to remove impurities such as a minute amount of gelled product. A small amount was extracted from the solution after filtration, and the solid content was measured in the same manner as in Example 1. As a result, it was 38.5% by mass. As a result of measuring the acid value of the polymer A in the same manner as in Example 1, it was 380 mg / g (theoretical acid value: 442.7 mg / g).

(2) Preparation of acrylamide phosphonic acid In an automatic synthesis reaction apparatus (internal volume 500 mL, manufactured by Unichemical Co., Ltd.) connected to a reflux condenser, a powder inlet, and a thermometer, 122.3 g ( 1.72 mol) of acrylamide and 1.0 g of hydroquinone monomethyl ether were dissolved and heated to 60 ° C. After confirming that the internal temperature reached 60 ° C., 134.0 g (0.94 mol) of phosphoric anhydride was added in 5 portions over 3 hours and 30 minutes from the powder inlet. While adding phosphoric anhydride, the internal temperature was maintained in the range of 60 to 95 ° C. while stirring at 300 to 400 rpm. After all the phosphoric anhydride was added, an aging reaction was performed at 80 ° C. for 2 hours.

  0.5 g was extracted from the resulting reaction solution, diluted with 5 g of methanol, dried in hot air at 100 ° C. for 1 hour, and the solid content was measured and found to be 63% by mass. 1 g of the reaction solution was dissolved in 100 g of dimethyl sulfoxide (DMSO), and the measured acid value (using a 1N aqueous KOH solution, titration end point: pH = 10.3) was 444 mg / g (converted to solid content, diacrylamide pyrol. Theoretical acid value of phosphonic acid: 394 mg / g, Theoretical acid value of diacrylamide dipyrophosphonic acid: 526 mg / g.) A part of the reaction solution was extracted and mixed with water, and it became cloudy. This is probably because water-insoluble acrylonitrile was by-produced.

  Since the reaction solution was cooled, a small amount of solid was precipitated, and the solid deposited by suction filtration was separated by filtration. 14.76 g (0.82 mol) of water was added to 330 g of the obtained transparent liquid, and hydrolyzed by heating at 70-80 ° C. for 30 minutes with stirring. 0.5 g was extracted from the resulting reaction solution, diluted with 5 g of methanol, dried in hot air at 100 ° C. for 1 hour, and the solid content was measured and found to be 64% by mass. The acid value (using 1N KOH aqueous solution, titration end point: pH = 10.3) measured using the obtained reaction solution after hydrolysis was 795.3 mg / g (in terms of solid content. Theoretical acid of acrylamide phosphonic acid) Value: 741.7 mg / g, Theoretical acid value of acrylamide diphosphonic acid: 969.7 mg / g.) The measured acid value is higher than the theoretical acid value (741.7 mg / g) because excess phosphoric anhydride was added, so that acrylamide diphosphonic acid and diphosphate residue and triphosphate represented by the above formula (9) This is probably because a monomer having a residue was formed.

  50 g of the obtained reaction solution after hydrolysis was poured into 500 g of THF little by little while stirring, thereby separating the upper impurity-containing THF and the purified lower-layer viscous liquid. This was separated with a separatory funnel, and only the lower layer purified viscous liquid was taken out. To prevent polymerization during vacuum drying, 0.003 g of hydroquinone monomethyl ether (MEHQ) was added, followed by vacuum drying at room temperature to obtain acrylamidephosphonic acid. A monomer composition (hereinafter referred to as “monomer NP” unless otherwise specified) was obtained.

  As a result of analyzing the monomer NP by liquid chromatography, the total content of acrylamide phosphonic acid, acrylamide diphosphonic acid, and the monomer having a diphosphate residue and a triphosphate residue represented by the above formula (9) Was 70% by mass or more, and in addition, it was confirmed that it contained 5% by mass or less of by-product acrylonitrile [analysis conditions for liquid chromatography are as follows. Measuring instrument: SPD-10A manufactured by Shimadzu Corporation (using UV detector), column temperature: room temperature, solvent: methanol / water = 7/3 (mass ratio), concentration: 0.01% by mass (injection amount: 2.5 μl) Column: PRP-1 manufactured by HAMILTON, solvent flow rate: 0.3 ml / min. ].

(3) Preparation of phosphonic acid group-containing tertiary butyl acrylamide sulfonic acid In the same reaction vessel as in (2) above, 207 g (1 mol) of tertiary butyl acrylamide sulfonic acid (TBAS: manufactured by Mitsubishi Rayon Co., Ltd.) and 1.0 g The hydroquinone monomethyl ether was dissolved in 200 g of DMF and heated to 70 ° C. After confirming that the internal temperature reached 70 ° C., 78 g (0.55 mol) of phosphoric anhydride was added in two portions over 2 hours from the powder inlet. While adding phosphoric anhydride, the internal temperature was maintained in the range of 70 to 95 ° C. while stirring at 300 to 400 rpm. After all the phosphoric anhydride was added, the aging reaction was performed at 70 to 95 ° C. for 1 hour.

  1 g of the reaction solution was dissolved in 100 g of DMSO, and the measured acid value (using a 1N KOH aqueous solution. End point of titration: pH = 10.3) was 404.0 mg / g [solid content (however, the solid content is a theoretical calculation value) . Theoretical acid value of di (tertiary butyl acrylamide sulfonic acid) pyrophosphonic acid: 402.9 mg / g].

  When 9.9 g (0.55 mol) of water was added to 486 g of the resulting reaction solution at 70 ° C., the temperature rose to 90 ° C. Then, it hydrolyzed by heating at 70-90 degreeC for 30 minutes with stirring. The acid value (using 1N KOH aqueous solution, titration end point: pH = 10.3) measured using the obtained reaction solution after hydrolysis was 594.6 mg / g (in terms of solid content. Phosphonic acid group-containing tertiary) Theoretical acid value of butylacrylamide sulfonic acid: 585.4 mg / g). As a result, it was judged that tertiary butyl acrylamide sulfonic acid containing phosphonic acid groups was synthesized.

  50 g of the obtained reaction solution after hydrolysis was poured into 500 g of THF little by little while stirring, thereby separating the upper impurity-containing THF and the purified lower-layer viscous liquid. This was separated with a separatory funnel, and only the lower layer purified viscous liquid was taken out. To prevent polymerization during vacuum drying, 0.003 g of hydroquinone monomethyl ether (MEHQ) was added, followed by vacuum drying at room temperature to obtain a phosphonic acid group. Containing tertiary butyl acrylamide sulfonic acid (hereinafter referred to as “monomer SNP” unless otherwise specified) was obtained.

(4) Preparation of phosphate esterified glycerol dimethacrylate 342 g (1.5 mol) of glycerol dimethacrylate [trade name “Blemmer GMR-H, hydroxyl equivalent: 239 (analytical)], Japan, in the same reaction vessel as above (2) “Oil / Fat Co., Ltd.” was added and the temperature was raised to 60 ° C. After confirming that the internal temperature reached 60 ° C, 117 g (0.825 mol) of phosphoric anhydride was added from the powder inlet into 6 times, approximately 1/6, and charged at approximately equal intervals over 6 hours. did. While adding phosphoric anhydride, the internal temperature was maintained in the range of 70 to 90 ° C. with stirring at 420 rpm. After all the phosphoric anhydride was added, the mixture was aged at 80 ° C. for 2 hours.

  The resulting solution was filtered through a wire mesh (100 mesh) to remove a trace amount of impurities such as polyphosphoric acid. The filtered solution was returned to the reaction vessel, stirred at 420 rpm, and heated to a liquid temperature of 80 to 85 ° C., and 22 g of water (1.22 mol) was added from the dropping funnel over 1 hour. The aging reaction was carried out at the same temperature for 2 hours. The acid value measured using the obtained reaction solution after hydrolysis [number of colors: 3, refractive index (20 ° C.): 1.4745] was 351 mg / g (theoretical acid of phosphate esterified glycerol dimethacrylate) Value: 363.6 mg / g). As a result, it was judged that phosphate esterified glycerol dimethacrylate (hereinafter referred to as “monomer GDM” unless otherwise specified) was synthesized.

(5) Production of solid polymer electrolyte membrane Polymer A DMAA solution prepared as described above, monomer NP, monomer SNP and monomer GDM, acrylonitrile (AN) and terminal acrylic modified liquid butadiene oligomer (NISSO-PB TE) -2000, Nippon Soda Co., Ltd.) were mixed to prepare a composition having the blending ratio shown in Table 4. As a polymerization initiator, [Irgacure 651 (2,2-dimethoxy-1,2-diphenylethane-1-one, manufactured by Ciba Specialty Chemicals) + Irgacure 500 (1-hydroxycyclohexyl phenyl ketone) was used as a polymerization initiator. , Benzophenone) + benzoyl peroxide (BPO) = 4.6 wt% + 2.4 wt% + 0.3 wt%] (vs. composition).

  A polyethylene film is affixed on a square glass plate with a side of 20 cm, a spacer tape with a thickness of 100 μm is attached to each end, a composition to which the above polymerization initiator is added at the center of the diagonal is dropped, and a polyethylene film is formed thereon. The glass plate on which was attached was placed, and the composition was sandwiched between two glass plates. In this state, photopolymerization was performed by irradiating the front and back with ultraviolet rays for 5 minutes each (irradiation distance: 20 cm) with a high-pressure mercury lamp (400 W). Furthermore, it heat-processed for 5 minutes at 500W using the microwave oven, and produced the 100-micrometer-thick solid polymer electrolyte membrane. The obtained film was transparent and excellent in uniformity.

Example 4
(1) Preparation of acrylamide diphosphonic acid 71 g (1 mol) of acrylamide was added to an automatic synthesis reactor (internal volume 500 mL, manufactured by Unichemical Co., Ltd.) connected to a reflux condenser, a powder inlet and a thermometer. And 1.0 g of hydroquinone monomethyl ether were added, dissolved in 198 g of dimethylacetamide, and heated to 60 ° C. After confirming that the internal temperature reached 60 ° C., 156 g (1.1 mol) of phosphoric anhydride was added in 5 portions over 3 hours and 30 minutes from the powder inlet. While adding phosphoric anhydride, the internal temperature was maintained in the range of 60 to 95 ° C. while stirring at 300 to 400 rpm. After all the phosphoric anhydride was added, an aging reaction was performed at 80 ° C. for 2 hours.

  0.5 g was extracted from the obtained reaction solution, diluted with 5 g of methanol, dried in hot air at 100 ° C. for 1 hour, and the solid content was measured. As a result, it was 53% by mass. The acid value (1N KOH aqueous solution used, titration end point: pH = 10.3) measured by dissolving 0.65 g of the reaction solution in 100 g of dimethylsulfoxide (DMSO) was 550 mg / g (in terms of solid content). Theoretical acid value of acrylamide pyrophosphonic acid and diacrylamide dipyrophosphonic acid: 525.8 mg / g). A part of the reaction solution was extracted and mixed with water, and it became cloudy. This is probably because water-insoluble acrylonitrile was by-produced.

  Subsequently, 20 g (1.1 mol) of water was added to the reaction solution, and the mixture was hydrolyzed by heating at 70-80 ° C. for 30 minutes with stirring. 0.5 g was extracted from the obtained reaction solution, diluted with 5 g of methanol, dried in hot air at 100 ° C. for 1 hour, and the solid content was measured. As a result, it was 55% by mass. The acid value (using 1N KOH aqueous solution, titration end point: pH = 10.3) measured using the obtained reaction solution after hydrolysis was 959.1 mg / g (in terms of solid content. Theoretical acid of acrylamide phosphonic acid) Value: 741.7 mg / g, Theoretical acid value of acrylamide diphosphonic acid: 969.7 mg / g).

  50 g of the obtained reaction solution after hydrolysis was poured into 500 g of THF little by little while stirring, thereby separating the upper impurity-containing THF and the purified lower-layer viscous liquid. This was separated using a separatory funnel, and only the lower-layer purified viscous liquid was taken out. To prevent polymerization during vacuum drying, 0.003 g of hydroquinone monomethyl ether (MEHQ) was added, followed by vacuum drying at room temperature to obtain acrylamide diphosphon. A monomer composition containing an acid as a main component (hereinafter referred to as “monomer N2P” unless otherwise specified) was obtained.

  The obtained monomer N2P was analyzed by liquid chromatography in the same manner as in Example 1. As a result, acrylamide phosphonic acid, acrylamide diphosphonic acid, and 2-phosphate residue and 3-phosphate represented by the above formula (11) were obtained. It was confirmed that the total content of the monomer having a residue was 90% by mass or more and that by-product acrylonitrile was further contained by 5% by mass or less.

(2) Production of solid polymer electrolyte membrane Polymer A DMAA solution, monomer NP, monomer SNP and monomer GDM prepared in the same manner as in Example 3, and monomers N2P, AN and terminal acrylic prepared in (1) above. The modified liquid butadiene oligomer was mixed to prepare a composition having a blending ratio shown in Table 4. [Irgacure 651 + Irgacure 500 + BPO = 4.6 wt% + 2.4 wt% + 0.3 wt%] (vs. composition) was added to the resulting composition as a polymerization initiator. Using the composition to which the polymerization initiator was added, a solid polymer electrolyte membrane having a thickness of 97 μm was produced in the same manner as in Example 3. The obtained film was transparent and excellent in uniformity.

Example 5
Polymer A DMAA solution prepared in the same manner as in Example 3, monomer NP, monomer SNP and monomer GDM, and AN and terminal acrylic-modified liquid butadiene oligomer were mixed to prepare a composition having a blending ratio shown in Table 4. . [Irgacure 651 + Irgacure 500 + BPO = 6.2 wt% + 3.0 wt% + 049 wt%] (vs. composition) was added to the obtained composition as a polymerization initiator. Using the composition to which the polymerization initiator was added, a solid polymer electrolyte membrane having a thickness of 104 μm was produced in the same manner as in Example 3. The obtained film was transparent and excellent in uniformity.

  The physical properties of the solid polymer electrolyte membranes prepared in Examples 3 to 5 were measured by the same method as in Example 1. The results are shown in Table 4.

Notes: (1) Polyvinyl alcohol containing vinyl acetate units that have been phosphated.
(2) Main component: Acrylamide phosphonic acid.
(3) Main component: Acrylamide diphosphonic acid.
(4) Tertiary butyl acrylamide sulfonic acid containing a phosphonic acid group.
(5) Phosphate esterified glycerol dimethacrylate.
(6) N, N-dimethylacrylamide.
(7) Acrylonitrile.
(8) NISSO-PB TE-2000, manufactured by Nippon Soda Co., Ltd.

Comparative Example 2
A solid polymer electrolyte membrane was produced in the same manner as in Example 3 except that the polymer A was not added. However, the obtained film was cloudy and inferior in uniformity as compared with Example 3.

As shown in Tables 3 and 4, the solid polymer electrolyte membranes of Examples 1 to 5 were slightly swelled by immersion in water, hot water, and methanol, but did not dissolve and were practically satisfactory. is there. Regarding the surface specific resistance value, the solid polymer electrolyte membranes of Examples 1 to 5 have a surface density of 1 × 10 ⁶ Ω or less under the condition of room temperature / RH = 50 to 75%, and the surface of a standard conductive resin composition It was superior to the specific resistance value. Further, from the results shown in Table 4, the proton conductivity of the solid polymer electrolyte membranes of Examples 2 to 5 is 10 ⁻⁴ to 10 ⁻² S under the measurement conditions of 35 to 80 ° C. and 90% relative humidity. -It was on the order of cm ^-1 and was a good level as a polymer electrolyte having a phosphate group as an acid group.

  The solid polymer electrolyte membranes of Examples 1 to 5 have (1) a hydrophobic portion made of a hydrocarbon skeleton in which vinyl groups are linked in a chain, and (2) a hydrophilic portion made of a phosphate group. It is estimated that the portion becomes an efficient proton conduction path. Moreover, since the solid polymer electrolyte membrane of Examples 1-5 has a fatty acid vinyl unit, it is thought that it is excellent in water resistance and solvent resistance.

  In particular, the solid polymer electrolyte membranes of Examples 3 to 5 are mainly composed of a phosphonic acid group-containing acrylamide polymer having a high phosphonic acid group density, and also include a conjugated diene-based liquid oligomer polymer. Therefore, it is considered that the phosphonic acid group further increases the density of the hydrophilic part, and the polymer of the conjugated diene liquid oligomer enhances the action of the hydrophobic part.

Claims (7)

(1) A first composition comprising a phosphate esterified unsaturated alcohol copolymer (A) and another conductive resin (B), or (2) the phosphate esterified unsaturated alcohol system A solid polymer electrolyte membrane having proton conductivity, comprising a second composition comprising a copolymer (A), the other conductive resin (B), and a non-conductive resin (C). ,
The phosphate esterified unsaturated alcohol copolymer (A) comprises (a) Formula (I):

The repeating unit (I) represented by the formula (II):

The total of the repeating units (I) and (II) is 100 mol%, the ratio of the repeating units (I) is 5 to 60 mol%, and the average degree of polymerization is 100 to 3,000 unsaturated alcohol copolymer, (b) anhydrous phosphoric acid, and (c) water or hydrogen peroxide solution are reacted to form a hydroxyl group of the unsaturated alcohol copolymer. It is a compound formed by substituting at least a part with -OP (O) (OH) ₂ group,
The other conductive resin (B) includes a phosphonic acid group-containing (meth) acrylamide derivative (B-1), a phosphoric acid group-containing unsaturated monomer (B-2), and a sulfonic acid group-containing unsaturated monomer. (B-3) and at least one acidic group-containing unsaturated monomer selected from the group consisting of phosphate esterified products of alcoholic hydroxyl group-containing unsaturated monomers (B-4) A compound,
The phosphonic acid group-containing (meth) acrylamide derivative (B-1) is at least selected from the group consisting of (meth) acrylamide phosphonic acid, (meth) acrylamide diphosphonic acid and phosphonic acid group-containing tertiary butyl acrylamide sulfonic acid. A kind,
The phosphate group-containing unsaturated monomer (B-2) is represented by (B-2-1) formula (13):

(Wherein R ¹⁰ is hydrogen or a methyl group, R ¹¹ is hydrogen or a substituted or unsubstituted alkyl group, and p is an integer of 1 to 6). A monomer, or (B-2-2) the phosphoric acid group-containing monoester unsaturated monomer, and the formula (14):

(However, R ¹⁰ and R ^{10 ′} are each independently a hydrogen group or a methyl group, R ¹¹ and R ^{11 ′} are each independently a hydrogen group or a substituted or unsubstituted alkyl group, and p ′ and p ″ are Each independently represents an integer of 1 to 6. The phosphoric acid group-containing diester unsaturated monomer represented by formula (15):

(However, R ¹⁰ and R ^{10 ′} are each independently a hydrogen group or a methyl group, R ¹¹ and R ^{11 ′} are each independently a hydrogen group or a substituted or unsubstituted alkyl group, and p ′ and p ″ are Each independently an integer of 1 to 6), or any of the pyrophosphate group-containing unsaturated monomers represented by
The sulfonic acid group-containing unsaturated monomer (B-3) includes tertiary butyl acrylamide sulfonic acid, allyl sulfonic acid, methallyl sulfonic acid, vinyl sulfonic acid, p-styrene sulfonic acid, butyl (meth) acrylate, 4-sulfonic acid or (meth) acryloxybenzenesulfonic acid,
The alcoholic hydroxyl group-containing unsaturated monomer phosphate ester (B-4) comprises glycerol di (meth) acrylate, 1,6-hexanediol diglycidyl ether acrylate, 1,4-butanediol diglycidyl ether acrylate , Bisphenol A type epoxy acrylate, and 2-hydroxy (meth) acrylate phosphoric acid ester,
The non-conductive resin (C) is melamine resin, polyvinyl alcohol, poly (meth) acrylonitrile, poly (meth) acrylic acid ester, polyacrylamide, polyacetal, water-soluble urethane resin, cellulose, polystyrene, polyvinyl chloride, polyacetic acid A group consisting of vinyl, vinyl aromatic-conjugated diene copolymer, polymer of conjugated diene liquid oligomer, polymer of alkylamino group-containing unsaturated monomer, and polymer of fluorine-containing unsaturated monomer At least one kind selected from
The conjugated diene-based liquid oligomer has the formula (19):

(However, R ¹⁴ and R ¹⁵ are each independently (a) a hydrocarbon group which has one or more ethylenically unsaturated bonds and may have other atomic groups, and (b) an ethylenically unsaturated bond. A hydrocarbon group which does not have and may have another atomic group or (c) a hydrogen group, and at least one of R ¹⁴ and R ¹⁵ has (a) a hydrocarbon having an ethylenically unsaturated bond R ¹⁶ and R ¹⁷ are each independently a hydrogen group or a methyl group, and at least one of R ¹⁶ and R ¹⁷ is a hydrogen group, and t represents the degree of polymerization.
The alkylamino group-containing unsaturated monomer includes N, N-dialkyl (meth) acrylamide, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (meth) acrylate, dimethylaminopropyl (meth) acrylate, dimethylaminobutyl (meth) ) Acrylate, dipropylaminoethyl (meth) acrylate, dibutylaminoethyl (meth) acrylate, dimethylaminoethyl (meth) acrylamide, diethylaminoethyl (meth) acrylamide, dimethylaminopropyl (meth) acrylamide, dimethylaminobutyl (meth) acrylamide , Dipropylaminoethyl (meth) acrylamide, or dibutylaminoethyl (meth) acrylamide,
The fluorine group-containing unsaturated monomer is hydrofluoroalkyl group-containing (meth) acrylic acid ester, perfluoroalkyl group-containing (meth) acrylic acid ester, hydrofluoroalkyl group-containing vinyl, or perfluoroalkyl group-containing vinyl. solid polymer electrolyte membrane, wherein there <br/> that. 2. The solid polymer electrolyte membrane according to claim 1 , wherein the phosphate esterified unsaturated alcohol copolymer (A) forms an ammonium salt, an amine salt or a metal salt. 3. Electrolyte membrane. In the solid polymer electrolyte membrane according to claim 1 or 2, wherein the conductive resin (B), together with the acidic group-containing unsaturated monomers, (meth) acrylonitrile, the conjugated diene-based liquid oligomer or hydrides thereof the alkylamino group-containing unsaturated monomers, (meth) acrylate acid ester le, styrene emission, vinyl chloride, vinyl acetate, the fluorinated group-containing unsaturated monomer, a vinyl aromatic - conjugated diene copolymer, At least one acidic group selected from the group consisting of ethylene glycol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, divinylbenzene, and urethane acrylate obtained by reacting diisocyanate with glycerol di (meth) acrylate. It looks including the free compound as a copolymerization component, and the acid group-containing unsaturated monomer A solid polymer electrolyte membrane having a mass ratio of 50/50 or more with the acid group-free compound . The solid polymer electrolyte membrane according to any one of claims 1 to 3, wherein the acidic group-containing unsaturated monomer of the other conductive resin (B) is the phosphonic acid group-containing (meth) acrylamide derivative. A solid polymer electrolyte membrane comprising (B-1) and a phosphoric acid ester (B-4) of the alcoholic hydroxyl group-containing unsaturated monomer. 5. The solid polymer electrolyte membrane according to claim 3, wherein the non-acidic group-containing compound of the other conductive resin (B) contains (meth) acrylonitrile, the conjugated diene-based liquid oligomer, and the alkylamino group. A solid polymer electrolyte membrane comprising an unsaturated monomer. The solid polymer electrolyte membrane according to any one of claims 1 to 5, wherein the phosphate esterified unsaturated alcohol copolymer (A) in the first composition and the other conductive resin. The solid content weight ratio to (B) is (95/5) to (40/60), the phosphate esterified unsaturated alcohol copolymer (A) in the second composition, and the others The solid content weight ratio of the conductive resin (B) and the non-conductive resin (C) to the total is (95/5) to (40/60), and the other conductive resin (B) and the above A solid polymer electrolyte membrane having a mass ratio of 50/50 or more to the non-conductive resin (C). A fuel cell comprising the solid polymer electrolyte membrane according to any one of claims 1 to 6 .