JP4935079B2 - Polymer composition containing oxocarbons and use thereof - Google Patents

Description

  The present invention relates to a polymer composition containing oxocarbons and use thereof.

Oxocarbons represented by squaric acid (square acid) are known to have high acidity because the structure in which hydrogen is dissociated from an oxocarbon group is stabilized by resonance (Non-patent Document 1) (Non-Patent Document 1) Patent Document 2).
On the other hand, polymer compounds having a sulfonic acid group are known to be useful as polymer electrolytes for polymer electrolyte fuel cells and the like. For example, fluorinated polymers such as Nafion (registered trademark of DuPont), polymers obtained by introducing sulfonic acid groups into polyether ketones (Patent Document 1), polymers obtained by introducing sulfonic acid groups into polyether sulfones (Non-patent Document 3), Polymers with sulfonic acid groups introduced into polyimides (Patent Document 2), Polymers with sulfonic acid groups introduced into polyphenylenes (Patent Document 3), and sulfonic acid groups introduced into polyphosphazenes The polymer (Non-patent Document 4) has been proposed as a polymer electrolyte for a polymer electrolyte fuel cell or the like.

Oxocarbons, p. 45 (Edited by Robert West), Academic Press (1980), (ISBN: 0-12-744580-3). Journal of the American Chemical Society, 95, 8703 (1973) J. et al. Membrane Science, 83, 211 (1993) Chemical Material, 3, 1120 (1991) US Pat. No. 5,438,082 JP 2003-277501 A US Pat. No. 5,403,675

However, a polymer composition containing oxocarbons is not known.
As a result of various studies, the present inventors have found that a polymer composition containing oxocarbons and a polymer compound is a solid polymer type using a gaseous fuel such as hydrogen gas or a liquid fuel such as methanol or dimethyl ether. It is found to be useful as a material for a proton conductive membrane of a fuel cell, that is, a polymer electrolyte, and has proton conductivity comparable to that of a polymer compound having a sulfonic acid group, and compared with a polymer compound having a sulfonic acid group. In addition, the inventors have found that the chemical stability and water resistance are excellent and that high proton conductivity can be maintained, and the present invention has been completed.
An object of the present invention is to provide a novel composition useful as a material for a proton conducting membrane of a solid polymer fuel cell, that is, a polymer electrolyte. When a proton conducting membrane is used, the chemical stability, water resistance An object of the present invention is to provide a composition that provides a proton conducting membrane having excellent properties and excellent proton conductivity.

（式中、Ｘ¹、Ｘ²はそれぞれ独立に−Ｏ−、−Ｓ−又は−ＮＲ’−を表し、Ｚは−ＣＯ−、−Ｃ（Ｓ）−、−Ｃ（ＮＲ’’）−、置換基を有していても良い炭素数１〜６のアルキレン基又は置換基を有していても良い炭素数６〜１０のアリーレン基を表す。ｎは、繰り返しの数を表わし、０〜１０の整数を表わす。Ｚが複数ある場合は、それぞれのＺは、互いに同じであっても良く、異なっていても良い。Ｒは、−ＯＨ、−ＳＨ、−ＮＨＲ’’’、置換基を有していても良い炭素数１〜１８のアルキル基、置換基を有していても良い炭素数６〜１８のアリール基又は置換基を有していても良い炭素数７〜１６のアラルキル基を表す。Ｒ’、Ｒ’’、Ｒ’’’は、それぞれ独立に水素原子、置換基を有していてもよい炭素数１〜６のアルキル基又は置換基を有していてもよい炭素数６〜１０のアリール基を表す。Ｂは、水素原子または１価の金属原子を表す。）
〔３〕Ｚが、−ＣＯ−、−Ｃ（Ｓ）−又は−Ｃ（ＮＨ）−のいずれかであることを特徴とする〔２〕記載の高分子組成物、
〔４〕Ｘ₁とＸ₂が−Ｏ−、Ｚが−ＣＯ−、ｎが０〜２の整数であることを特徴とする〔２〕〜〔３〕のいずれかに記載の高分子組成物、
〔５〕高分子化合物が、ポリビニルピロリドン類、ポリ（メタ）アクリル酸類、ポリ（メタ）アクリル酸エステル類、ポリ（メタ）アクリロニトリル類、ポリスチレン類、ポリビニルピリジン類、ポリエチレン類、ポリプロピレン類、ポリブテン類、ポリビニリデンフルオリド類、ポリテトラフルオロエチレン類、ポリ塩化ビニル類、ポリオキシアルキレン類、ポリシロキサン類、ポリエステル類、ポリイミド類、ポリアミド類、ポリベンズオキサゾール類、ポリベンズイミダゾール類、ポリアリーレンエーテル類、ポリアリーレン類、ポリアリーレンスルフィド類、ポリエーテルケトン類、ポリエーテルスルホン類、ポリホスファゼン類からなる群より選ばれる少なくとも１種であることを特徴とする〔１〕〜〔４〕のいずれかに記載の高分子組成物、
〔６〕［オキソカーボン類の物質量（ｍｍｏｌ）］／［高分子化合物の重量（ｇ）＋オキソカーボン類の重量（ｇ）］が０．０５〜８ｍｍｏｌ／ｇであることを特徴とする〔１〕〜〔５〕のいずれかに記載の高分子組成物、
〔７〕前記の〔１〕〜〔６〕のいずれかに記載の高分子組成物を有効成分とする高分子電解質、
〔８〕前記の〔７〕記載の高分子電解質を有することを特徴とする高分子電解質膜、
〔９〕前記の〔７〕に記載の高分子電解質または〔８〕に記載の高分子電解質膜の少なくとも一つを有することを特徴とする電池、
〔１０〕前記の〔７〕に記載の高分子電解質または〔８〕に記載の高分子電解質膜の少なくとも一つを用いることを特徴とする燃料電池、
〔１１〕前記の一般式（１）で示される化合物であって、Ｒがハロゲノ置換アリール基であることを特徴とするオキソカーボン化合物、
〔１２〕ハロゲノ置換アリール基が下式（２ａ）〜（２ｃ）からなる群より選ばれる基であることを特徴とする〔１１〕記載のオキソカーボン化合物、

（式中、ｐは１〜５の整数を表す。ｑは０〜３の整数、ｒは０〜４の整数を表し、かつ（ｑ＋ｒ）の値が１〜７である。ｓは０〜４の整数、ｔは０〜５の整数を表し、かつ（ｓ＋ｔ）の値が１〜９である。Ｙ¹〜Ｙ⁵はそれぞれ独立にハロゲノ基を表し、Ｙ¹〜Ｙ⁵がそれぞれ複数あるときにはこれらは同じであっても良いし異なっていても良い。）
〔１３〕ハロゲノ基がフルオロ基であることを特徴とする〔１２〕に記載のオキソカーボン化合物、
〔１４〕ハロゲノ置換アリール基が前記の（２ａ）であることを特徴とする〔１１〕〜〔１３〕のいずれかに記載のオキソカーボン化合物、
〔１５〕下式（３）で表されるオキソカーボン化合物、

〔１６〕下式（４）で表されるオキソカーボン化合物

に係るものである。 That is, the present invention relates to a polymer composition comprising [1] oxocarbons and a polymer compound.
Further, the present invention provides the polymer composition according to [1], wherein [2] oxocarbons are represented by the following formula (1):

Wherein X ¹ and X ² each independently represent —O—, —S— or —NR′—, Z represents —CO—, —C (S) —, —C (NR ″) —, Represents an optionally substituted alkylene group having 1 to 6 carbon atoms or an optionally substituted arylene group having 6 to 10 carbon atoms, n represents the number of repetitions, and 0 to 10 In the case where there are a plurality of Z, each Z may be the same as or different from each other.R is —OH, —SH, —NHR ′ ″, and has a substituent. An optionally substituted alkyl group having 1 to 18 carbon atoms, an optionally substituted aryl group having 6 to 18 carbon atoms, or an optionally substituted aralkyl group having 7 to 16 carbon atoms. R ′, R ″, and R ′ ″ each independently have a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, or a substituent. .B to an aryl group which may having 6 to 10 carbon atoms optionally represents a hydrogen atom or a monovalent metal atom.)
[3] The polymer composition according to [2], wherein Z is any one of —CO—, —C (S) —, and —C (NH) —.
[4] The polymer composition according to any one of [2] to [3], wherein X ₁ and X ₂ are —O—, Z is —CO—, and n is an integer of 0 to 2. ,
[5] The polymer compound is polyvinyl pyrrolidone, poly (meth) acrylic acid, poly (meth) acrylic acid ester, poly (meth) acrylonitrile, polystyrene, polyvinyl pyridines, polyethylene, polypropylene, polybutenes , Polyvinylidene fluorides, polytetrafluoroethylenes, polyvinyl chlorides, polyoxyalkylenes, polysiloxanes, polyesters, polyimides, polyamides, polybenzoxazoles, polybenzimidazoles, polyarylene ethers Any one of [1] to [4], characterized in that it is at least one selected from the group consisting of polyarylenes, polyarylene sulfides, polyether ketones, polyether sulfones, and polyphosphazenes Listed high Child composition,
[6] A feature of [amount of substance of oxocarbons (mmol)] / [weight of polymer compound (g) + weight of oxocarbons (g)] is 0.05 to 8 mmol / g [ 1] to [5], the polymer composition according to any one of
[7] A polymer electrolyte comprising the polymer composition according to any one of [1] to [6] as an active ingredient,
[8] A polymer electrolyte membrane comprising the polymer electrolyte according to [7] above,
[9] A battery comprising at least one of the polymer electrolyte according to [7] or the polymer electrolyte membrane according to [8],
[10] A fuel cell using at least one of the polymer electrolyte according to [7] or the polymer electrolyte membrane according to [8],
[11] An oxocarbon compound represented by the above general formula (1), wherein R is a halogeno-substituted aryl group,
[12] The oxocarbon compound according to [11], wherein the halogeno-substituted aryl group is a group selected from the group consisting of the following formulas (2a) to (2c):

(In the formula, p represents an integer of 1 to 5. q represents an integer of 0 to 3, r represents an integer of 0 to 4, and (q + r) has a value of 1 to 7. s represents 0 to 4). , T represents an integer of 0 to 5 and (s + t) has a value of 1 to 9. Y ^{1 to} Y ⁵ each independently represents a halogeno group, and when there are a plurality of Y ^{1 to} Y ⁵ These may be the same or different.)
[13] The oxocarbon compound according to [12], wherein the halogeno group is a fluoro group,
[14] The oxocarbon compound according to any one of [11] to [13], wherein the halogeno-substituted aryl group is the above (2a),
[15] An oxocarbon compound represented by the following formula (3):

[16] Oxocarbon compound represented by the following formula (4)

It is related to.

  The polymer composition containing oxocarbons of the present invention is useful as a material for a proton conductive membrane of a polymer electrolyte fuel cell using a gaseous fuel such as hydrogen gas or a liquid fuel such as methanol or dimethyl ether, that is, a polymer electrolyte. is there. In particular, it not only has proton conductivity comparable to a polymer compound having a sulfonic acid group, but also has excellent chemical stability, water resistance, etc. compared to a polymer compound having a sulfonic acid group, and is high over a long period of time. Since proton conductivity can be maintained, the polymer composition of the present invention is advantageous in practical use.

（式中、Ｘ¹、Ｘ²はそれぞれ独立に−Ｏ−、−Ｓ−又は−ＮＲ’−を表し、Ｚは−ＣＯ−、−Ｃ（Ｓ）−、−Ｃ（ＮＲ’’）−、置換基を有していても良い炭素数１〜６のアルキレン基又は置換基を有していても良い炭素数６〜１０のアリーレン基を表す。ｎは、繰り返しの数を表わし、０〜１０の整数を表わす。Ｚが複数ある場合は、それぞれのＺは、互いに同じであっても良く、異なっていても良い。Ｒは、−ＯＨ、−ＳＨ、−ＮＨＲ’’’、置換基を有していても良い炭素数１〜１８のアルキル基、置換基を有していても良い炭素数６〜１８のアリール基又は置換基を有していても良い炭素数７〜１６のアラルキル基を表す。Ｒ’、Ｒ’’、Ｒ’’’は、それぞれ独立に水素原子、置換基を有していてもよい炭素数１〜６のアルキル基又は置換基を有していてもよい炭素数６〜１０のアリール基を表す。Ｂは、水素原子または１価の金属原子を表す。） Hereinafter, the present invention will be described in detail.
The polymer composition of the present invention is characterized by containing oxocarbons and a polymer compound. The form of the composition is not particularly limited, but may be compatible at the molecular level or in an incompatible state. It is preferable because the proton conductivity of the proton conducting membrane that can obtain a compatible form at the molecular level is high.
The polymer electrolyte membrane of the present invention is a membrane comprising the above-described polymer composition as an active ingredient, and specifically, a membrane formed from the polymer composition may be used as a porous base material, woven fabric, non-woven fabric. The above-mentioned polymer composition may be impregnated.
When the polymer electrolyte is in the form of a film, the surface of the film may be coated with oxocarbons.
Here, typical examples of the oxocarbons include compounds represented by the following formula (1).

Wherein X ¹ and X ² each independently represent —O—, —S— or —NR′—, Z represents —CO—, —C (S) —, —C (NR ″) —, Represents an optionally substituted alkylene group having 1 to 6 carbon atoms or an optionally substituted arylene group having 6 to 10 carbon atoms, n represents the number of repetitions, and 0 to 10 In the case where there are a plurality of Z, each Z may be the same as or different from each other.R is —OH, —SH, —NHR ′ ″, and has a substituent. An optionally substituted alkyl group having 1 to 18 carbon atoms, an optionally substituted aryl group having 6 to 18 carbon atoms, or an optionally substituted aralkyl group having 7 to 16 carbon atoms. R ′, R ″, and R ′ ″ each independently have a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, or a substituent. .B to an aryl group which may having 6 to 10 carbon atoms optionally represents a hydrogen atom or a monovalent metal atom.)

で表わされる平衡反応をとりうる。この平衡反応の極限構造は下記式

のように表わされ、プロトンが解離した時のカチオンが分子内に広く非局在化するために安定な構造である。そのために式（１）で表される化合物は酸性度が高い化合物になるものと考えられる。 In the oxocarbons represented by the formula (1), when B is a hydrogen atom, that is, in the form of a free acid, the following formula

The equilibrium reaction represented by can be taken. The ultimate structure of this equilibrium reaction is

This is a stable structure because the cations when protons dissociate are widely delocalized in the molecule. Therefore, it is considered that the compound represented by the formula (1) becomes a compound having a high acidity.

In the oxocarbons represented by the formula (1), X ¹ and X ² each independently represent —O—, —S— or —NR′—. R ′ is a hydrogen atom; an alkyl group having 1 to 6 carbon atoms which may have a substituent represented by a methyl group, a trifluoromethyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, or the like. Alternatively, it represents an aryl group having 6 to 10 carbon atoms which may have a substituent represented by a phenyl group, a pentafluorophenyl group, a naphthyl group, or the like. R ′ is preferably a hydrogen atom. X ¹ and X ² are preferably —O— or —S—, and particularly preferably —O—.
Z may have -CO-, -C (S)-, -C (NR '')-, an optionally substituted alkylene group having 1 to 6 carbon atoms or a substituent. An arylene group having 6 to 10 carbon atoms is represented. R ″ is a hydrogen atom; an alkyl group having 1 to 6 carbon atoms which may have a substituent represented by a methyl group, a trifluoromethyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, or the like. Represents an aryl group having 6 to 10 carbon atoms which may have a substituent represented by a group or a phenyl group, a pentafluorophenyl group, a naphthyl group or the like. R ″ is preferably a hydrogen atom.
Here, as a C1-C6 alkylene group, a methylene group, ethylene group, a propylene group, i-propylene group, a butylene group, a pentylene group etc. are mentioned, for example. Examples of the arylene group having 6 to 10 carbon atoms include a phenylene group and a naphthylene group. In the case of having a substituent, examples of the substituent include halogeno groups such as a fluoro group, a chloro group, and a bromo group, and among them, a fluoro group is preferably used.
Z is preferably —CO—, —C (S) —, —C (NR ″) —, methylene, difluoromethylene, phenylene, tetrafluorophenylene, etc., more preferably —CO—, —C (S )-And the like, particularly preferably -CO- and the like.
n represents the number of repetitions of Z, and represents a number of n = 0 to 10. When n is 0, it means a single bond. The n Zs may be the same or different. n is preferably 0 to 4, more preferably 0 to 2, and particularly preferably 1.

R is —OH, —SH, —NHR ′ ″, an optionally substituted alkyl group having 1 to 18 carbon atoms, an optionally substituted aryl group having 6 to 18 carbon atoms, or An aralkyl group having 7 to 16 carbon atoms which may have a substituent is represented. R ′ ″ represents a hydrogen atom; optionally having a substituent represented by a methyl group, a trifluoromethyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, etc. It represents an aryl group having 6 to 10 carbon atoms which may have a substituent represented by an alkyl group, a phenyl group, a pentafluorophenyl group, a naphthyl group or the like. R ′ ″ is preferably a hydrogen atom.
Here, examples of the alkyl group having 1 to 18 carbon atoms include a methyl group, an ethyl group, a propyl group, an i-propyl group, an n-butyl group, a sec-butyl group, an isobutyl group, a t-butyl group, a pentyl group, Examples include hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group and the like.
Examples of the substituent when the alkyl group having 1 to 18 carbon atoms has a substituent include halogeno groups such as a fluoro group, a chloro group, and a bromo group; a nitro group; a cyano group; a methoxy group, an ethoxy group, and a propoxy group. C1-C5 alkoxy groups; C1-C5 fluoroalkyl groups, such as a trifluoromethyl group and a pentafluoromethyl group, etc. are mentioned.

が挙げられる。
式中、Ｙ¹〜Ｙ⁵はそれぞれ独立にハロゲノ基を表す。ｐは１〜５の整数を表す。ｑは０〜３の整数、ｒは０〜４の整数を表し、かつ（ｑ＋ｒ）の値が１〜７である。ｓは０〜４の整数、ｔは０〜５の整数を表し、かつ（ｓ＋ｔ）の値が１〜９である。Ｙ¹〜Ｙ⁵がそれぞれ複数あるときにはこれらは同じであっても良いし異なっていても良い。
ハロゲノ基として好ましくはフルオロ基、クロロ基であり、特に好ましくはフルオロ基である。（２ａ）〜（２ｄ）の中で特に好ましくは（２ａ）である。
炭素数７〜１６のアラルキル基としては、例えばベンジル基、フェニルエチル基、フェニルプロピル基、ナフチルメチル基、ナフチルエチル基等が挙げられる。炭素数７〜１６のアラルキル基が置換基を有する場合の置換基としては、例えばフルオロ基、クロロ基、ブロモ基等のハロゲノ基、ニトロ基、シアノ基、メトキシ基、エトキシ基、プロポキシ基等の炭素数１〜５のアルコキシ基、トリフルオロメチル基、ペンタフルオロメチル基等の炭素数１〜５のフルオロアルキル基、メチル基、エチル基、プロピル基、ブチル基等の炭素数１〜５のアルキル基などが挙げられる。
Ｒは、−ＯＨ、−ＳＨ、メチル基、エチル基、トリフルオロメチル基、フェニル基、ナフチル基、ペンタフルオロフェニル基、ベンジル基等であることが好ましく、より好ましくは−ＯＨ、フェニル基、ペンタフルオロフェニル基等である。 Moreover, as a C6-C18 aryl group, a phenyl group, a naphthyl group, an anthranyl group etc. are mentioned, for example. Examples of the substituent when the aryl group having 6 to 18 carbon atoms has a substituent include a halogeno group such as a fluoro group, a chloro group, and a bromo group, a nitro group, a cyano group, a methoxy group, an ethoxy group, and a propoxy group. C1-C5 fluoroalkyl group such as C1-C5 alkoxy group, trifluoromethyl group, pentafluoromethyl group, etc., C1-C5 alkyl such as methyl group, ethyl group, propyl group, butyl group Etc.
As an example of a C6-C18 aryl group which has a halogeno group as a substituent, for example, the following general formulas (2a) to (2d)

Is mentioned.
Wherein, Y ¹ to Y ⁵ each independently represent a halogeno group. p represents an integer of 1 to 5. q represents an integer of 0 to 3, r represents an integer of 0 to 4, and (q + r) has a value of 1 to 7. s represents an integer of 0 to 4, t represents an integer of 0 to 5, and (s + t) has a value of 1 to 9. When there are a plurality of Y ^{1 to} Y ⁵ , these may be the same or different.
The halogeno group is preferably a fluoro group or a chloro group, and particularly preferably a fluoro group. Among (2a) to (2d), (2a) is particularly preferable.
Examples of the aralkyl group having 7 to 16 carbon atoms include benzyl group, phenylethyl group, phenylpropyl group, naphthylmethyl group, naphthylethyl group and the like. Examples of the substituent when the aralkyl group having 7 to 16 carbon atoms has a substituent include a halogeno group such as a fluoro group, a chloro group, and a bromo group, a nitro group, a cyano group, a methoxy group, an ethoxy group, and a propoxy group. C1-C5 fluoroalkyl group such as C1-C5 alkoxy group, trifluoromethyl group, pentafluoromethyl group, etc., C1-C5 alkyl such as methyl group, ethyl group, propyl group, butyl group Group and the like.
R is preferably —OH, —SH, methyl group, ethyl group, trifluoromethyl group, phenyl group, naphthyl group, pentafluorophenyl group, benzyl group, and more preferably —OH, phenyl group, penta A fluorophenyl group and the like;

B represents a hydrogen atom or a monovalent metal atom. Examples of the monovalent metal atom include a lithium atom, a sodium atom, a potassium atom, a cesium atom, and a silver atom. B is preferably a hydrogen atom, a lithium atom, a sodium atom, a potassium atom or a cesium atom, more preferably a lithium atom, a sodium atom or a potassium atom, still more preferably a hydrogen atom or a lithium atom.
When the composition of the present invention is used as an electrolyte for a lithium secondary battery, lithium is used as B.
When the composition of the present invention is used in a polymer electrolyte fuel cell, it is preferable that substantially all functional groups are in the form of a free acid, that is, B is a hydrogen atom.

Specific examples of the oxocarbons represented by the formula (1) in the present invention include the following compounds. Here, the case where B is a hydrogen atom is illustrated.

  In the present invention, the above oxocarbons are used. Among these, (a1) to (a66) are preferable. More preferably (a2), (a5) (a8), (a11), (a14), (a17), (a20), (a23), (a26), (a29), (a32), (a35), (A38), (a41), (a44), (a47), (a50), (a53), (a56), (a59), (a62), (a65), and more preferably (a2), (A5), (a17), (a26), (a29), (a41), (a44), (a50), (a53), (a59), (a62), (a65), particularly preferably ( a2), (a41), (a50), and (a53).

Oxocarbons can be produced, for example, according to the following method. Moreover, you may obtain from a reagent maker.
(I) A method for producing a compound in which R in the oxocarbons (1) is alkyl or aryl using a lithium reagent (Journal of Organic Chemistry, 53 , 2482, 2477 (1988)).
(II) A method for producing a compound in which R in the oxocarbons (1) is alkyl or aryl using a Grignard reagent (Heterocycles, 27 (5), 1191 (1988)).
(III) A method for producing a compound in which R in the oxocarbons (1) is alkyl or aryl using a tin reagent (Journal of Organic Chemistry, 55 , 5359 (1990), Tetrahydron Letters, 31 (30), 4293 (1990)).
(IV) A method of synthesis using Friedel Crafts reaction (Synthesis, page 46 (1974)).
Various derivatives can be synthesized by complying with these methods. When an ester is obtained by the methods (I) to (IV), an oxocarbon in which B in the general formula (1) is a hydrogen atom is obtained by hydrolyzing the ester with an acid or alkali. Can do. When B in the general formula (1) is an alkali metal, it can be obtained by neutralizing oxocarbons in which B is a hydrogen atom with a solution containing an alkali metal hydroxide. Formula (1) is shown in the form of a free acid, but when the hydrogen atom shown in Formula (1) is replaced with a monovalent metal ion, the free shown in Formula (1) It can be obtained by neutralizing acid oxocarbons with a solution containing an alkali metal hydroxide.

The polymer composition of the present invention comprises the above oxocarbons and a polymer compound.
Here, as the polymer compound, for example, polyvinylpyrrolidones, poly (meth) acrylic acids, poly (meth) acrylic esters, poly (meth) acrylonitriles, polystyrenes, polyvinylpyridines, polyethylenes, polypropylenes, Vinyl polymers represented by polybutenes, polyvinylidene fluorides, polytetrafluoroethylenes, polyvinyl chlorides, polyoxyalkylenes, polysiloxanes, polyesters, polyimides, polyamides, polybenzoxazoles Polybenzimidazoles, polyarylene ethers, polyarylenes, polyarylene sulfides, polyether ketones, polyether sulfones, polyphosphazenes, etc., copolymers thereof and mixtures thereof. It is.
Of these, polyvinylpyrrolidones, poly (meth) acrylic esters, poly (meth) acrylonitriles, polystyrenes, polyvinylpyridines, polyvinylidene fluorides, polytetrafluoroethylenes, polyesters, polyimides, poly Benzoxazoles, polybenzimidazoles, polyarylene ethers, polyarylenes, polyether ketones, polyether sulfones and copolymers thereof, and mixtures thereof, more preferably polyvinylpyrrolidones, polystyrenes , Polyvinyl pyridines, polybenzimidazoles, polyether sulfones and copolymers thereof, and mixtures thereof.
The molecular weight of the polymer is usually 1000 or more in terms of number average, and when used in a film shape, 5000 or more is preferable from the viewpoint of maintaining the shape as a film. The number average molecular weight is usually about 2 million or less, and when used in a film shape, it is preferably about 1000000 or less from the viewpoint of moldability to a film.

The composition of the present invention containing the polymer compound as described above and the oxocarbons as described above is [substance amount of oxocarbons (mmol)] / [weight of polymer compound (g) + oxocarbon. Weight (g)], that is, the equivalent amount of oxocarbons in the composition is preferably 0.05 to 8 mmol / g, more preferably 0.1 to 7 mmol / g, and particularly preferably 0.3. -6 mmol / g, most preferably 0.5-5 mmol / g.
Here, the equivalent of oxocarbons in the composition is preferably 0.05 mmol / g or more because ion conductivity tends to be further improved, and 8 mmol / g or less is more preferable in terms of water resistance. There is a tendency.
The oxocarbons are usually used so that the equivalent amount of the oxocarbons in the composition falls within the above range. The quantification of oxocarbons in the composition of the present invention is determined using NMR method.

The polymer composition of the present invention is characterized by containing a polymer compound and oxocarbons, and its production method is not particularly limited. For example, the polymer compound and oxocarbons are used as a solvent. Examples thereof include a method obtained by dissolving, dispersing or suspending and mixing and then removing the solvent, and a method obtained by synthesizing a polymer in the presence of oxocarbons.
Here, as the solvent in the former method, for example, water, alcohol solvent, ketone solvent, ether solvent, halogen solvent, sulfoxide solvent, sulfone solvent, amide solvent, aliphatic hydrocarbon solvent, aromatic solvent It selects suitably from a group hydrocarbon solvent, these mixed solvents, etc.
Examples of alcohol solvents include methanol, ethanol, isopropanol, butanol, and examples of ketone solvents include acetone, methyl isobutyl ketone, methyl ethyl ketone, and benzophenone. Examples of ether solvents include diethyl ether, dibutyl ether, diphenyl ether, tetrahydrofuran (hereinafter abbreviated as THF), dioxane, dioxolane, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, and the like. It is done.

Examples of the halogen-based solvent include chloroform, dichloromethane, 1,2-dichloroethane, 1,1,2,2-tetrachloroethane, chlorobenzene, and dichlorobenzene. Examples of the sulfoxide-based solvent include dimethyl sulfoxide (hereinafter abbreviated as DMSO). It is done. Examples of the sulfone solvent include diphenyl sulfone and sulfolane, and examples of the amide solvent include N, N-dimethylacetamide (hereinafter abbreviated as DMAc), N-methylacetamide, N, N-dimethylformamide (hereinafter abbreviated as DMF), N-methylformamide, formamide, N-methylpyrrolidone (hereinafter abbreviated as NMP) and the like. Examples of the aliphatic hydrocarbon solvent include pentane, hexane, heptane, and octane, and examples of the aromatic hydrocarbon solvent include benzene, toluene, xylene, and the like.
Among these, it is preferable to select from water, alcohol solvents, ether solvents, halogen solvents, amide solvents, and mixed solvents thereof. More preferably, it is selected from water, methanol, THF, dichloromethane, DMAc, and mixed solvents thereof.

  Examples of the method for removing the solvent include a method of evaporating and evaporating the solvent of the mixed solution, dispersion or suspension, and the like, but it may be formed into a film by using the solvent casting method described later. Is possible.

  Further, as a method for obtaining a polymer composition by synthesizing a polymer in the presence of oxocarbons, known polymerization methods such as radical polymerization, cationic polymerization, anionic polymerization, Zieglar- Polymers are synthesized using ion polymerization, ring-opening polymerization, elimination polymerization, polyaddition, polycondensation, addition condensation, etc. using Natta catalyst ("Experimental Methods for Polymer Synthesis", Chemical Dojin 125-357) Page (1972)) and a method for obtaining a polymer composition. In the polymerization reaction, when the oxocarbons can cause a side reaction that inhibits the polymerization, for example, when anionic polymerization is carried out in the presence of oxocarbons having a hydroxyl group, this group can be converted to, for example, an alkoxy group or a siloxy group. The hydroxyl group can be protected and used by a known protection method of protecting with a group, an ester group or the like. In this case, the desired product can be obtained by removing the protective group by a known method after polymerization.

Next, the case where the polymer composition of the present invention is used as a diaphragm of an electrochemical device such as a fuel cell will be described.
In this case, the polymer composition of the present invention is usually used in the form of a film, but there is no particular limitation on the method of converting into a film, and for example, a method of forming a film from a solution state (solvent casting method) is preferably used. The
Specifically, the polymer composition is dissolved in an appropriate solvent, the solution is applied onto a glass plate, and the solvent is removed to form a film. The solvent used for film formation is not particularly limited as long as it can dissolve the polymer composition and can be removed thereafter, and is an aprotic polar solvent such as DMF, DMAc, NMP, DMSO, or dichloromethane, Chlorinated solvents such as chloroform, 1,2-dichloroethane, chlorobenzene, dichlorobenzene, alcohols such as methanol, ethanol, propanol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, etc. Alkylene glycol monoalkyl ether, THF, 1,3-dioxolane, 1,4-dioxane, 1,3-dioxane, tetrahydropyran, dibutyl ether, tert-butyl methyl ether, di Phenyl ether, ether solvents such as crown ethers are preferably used. These can be used singly, but two or more solvents can be mixed and used as necessary.
Among these, DMSO, DMF, DMAc, NMP, THF, 1,3-dioxolane and the like are preferable because of high solubility of the polymer composition.

  Although there is no restriction | limiting in particular in the thickness of a film, 10-300 micrometers is preferable and 20-100 micrometers is especially preferable. When the film is thinner than 10 μm, the practical strength may not be sufficient, and when the film is thicker than 300 μm, the film resistance tends to increase and the characteristics of the electrochemical device tend to deteriorate. The film thickness can be controlled by the concentration of the solution and the coating thickness on the substrate.

For the purpose of improving various physical properties of the film, the polymer composition of the present invention may contain plasticizers, stabilizers, mold release agents and the like used in ordinary polymer compounds. Also, other polymers can be combined with the polymer composition of the present invention by a method such as co-casting in the same solvent.
In fuel cell applications, it is also known to add inorganic or organic fine particles as a water retention agent in order to facilitate water management. Any of these known methods can be used as long as they are not contrary to the object of the present invention.
Further, for the purpose of improving the mechanical strength of the film, it can also be crosslinked by irradiating with an electron beam, radiation or the like (for example, JP-A-11-111310). Furthermore, a porous film or sheet is impregnated and composited (Japanese Patent Laid-Open No. 6-29032), or a method of reinforcing a film by mixing fibers or pulp is known. Can be used as long as the object of the present invention is not violated.

The battery of the present invention has at least one of the polymer electrolyte or the polymer electrolyte membrane of the present invention. Here, examples of the battery include a fuel cell, a lithium ion secondary battery, and the like, and a fuel cell is particularly preferable. Among the fuel cells, a polymer electrolyte fuel cell is most preferable.
Next, the fuel cell of the present invention will be described.
The fuel cell of the present invention has at least one of the polymer electrolyte or the polymer electrolyte membrane of the present invention.
The fuel cell of the present invention can be produced by bonding a catalyst and a conductive material as a current collector to both surfaces of a film.
The catalyst is not particularly limited as long as it can activate the oxidation-reduction reaction with hydrogen or oxygen, and a known catalyst can be used, but platinum fine particles are preferably used. The fine particles of platinum are often used by being supported on particulate or fibrous carbon such as activated carbon or graphite.
A known material can be used for the conductive material as the current collector, but porous carbon woven fabric, carbon non-woven fabric, or carbon paper is preferable in order to efficiently transport the raw material gas to the catalyst.
For a method of bonding platinum fine particles or carbon carrying platinum fine particles to a porous carbon nonwoven fabric or carbon paper, and a method of bonding it to a polymer electrolyte film, see, for example, J. Org. Electrochem. Soc. : Known methods such as those described in Electrochemical Science and Technology, 1988, 135 (9), 2209 can be used.
The polymer composition of the present invention can also be used as a proton conductive material that is a component of the catalyst composition constituting the catalyst layer of the polymer electrolyte fuel cell.
The fuel cell of the present invention thus produced can be used in various forms using hydrogen gas, reformed hydrogen gas, methanol, dimethyl ether, etc. as fuel.

（式中、ｐは１〜５の整数を表す。ｑは０〜３の整数、ｒは０〜４の整数を表し、かつ（ｑ＋ｒ）の値が１〜７である。ｓは０〜４の整数、ｔは０〜５の整数を表し、かつ（ｓ＋ｔ）の値が１〜９である。Ｙ¹〜Ｙ⁵はそれぞれ独立にハロゲノ基を表し、Ｙ¹〜Ｙ⁵がそれぞれ複数あるときにはこれらは同じであっても良いし異なっていても良い。）
該ハロゲノ置換アリール基において、該ハロゲノ基がフルオロ基であることが好ましい。このような化合物として、具体的には既述の（ａ４９）〜（a５４）、（ａ５８）〜（ａ６６）、（ｂ４９）〜（ｂ５４）、（ｂ５８）〜（ｂ６６）、（ｃ４９）〜（ｃ５４）、（ｃ５８）〜（ｃ６６）が挙げられる。 Next, the oxocarbon compound of the present invention will be described.
The oxocarbon compound of the present invention is a compound represented by the above general formula (1), wherein R is a halogeno-substituted aryl group.
As described above, since the polymer composition containing the oxocarbon compound and the polymer compound is excellent in proton conductivity, it can be suitably used for an electrolyte membrane of a fuel cell.
Examples of the oxocarbon compound of the present invention include compounds in which the halogeno-substituted aryl group is a group selected from the group consisting of the following formulas (2a) to (2c).

(In the formula, p represents an integer of 1 to 5. q represents an integer of 0 to 3, r represents an integer of 0 to 4, and (q + r) has a value of 1 to 7. s represents 0 to 4). , T represents an integer of 0 to 5 and (s + t) has a value of 1 to 9. Y ^{1 to} Y ⁵ each independently represents a halogeno group, and when there are a plurality of Y ^{1 to} Y ⁵ These may be the same or different.)
In the halogeno-substituted aryl group, the halogeno group is preferably a fluoro group. Specific examples of such compounds include (a49) to (a54), (a58) to (a66), (b49) to (b54), (b58) to (b66), and (c49) to (c49) described above. c54) and (c58) to (c66).

  Since the oxocarbon compound of the present invention has high proton conductivity, the halogeno-substituted aryl group is preferably (2a). Among these, (a49) to (a54), (b49) to (b54), and (c49) to (c54) described above are preferable. Among these, (a49) to (a54) are more preferable, and (a50) and (a53) are particularly preferable.

また、本発明のオキソカーボン化合物として、もう一つの具体的な構造式としては（ａ５３）で表される下式（４）で表されるオキソカーボン化合物が挙げられる。

Ｒがハロゲノ置換アリール基であるオキソカーボン化合物としては上記のようなものが挙げられるが、これらはプロトン酸としての性質を有する遊離酸の形で用いてもよいし、遊離酸が一価の金属原子で置換され、中和された形でもよい。１価の金属原子としては、リチウム原子、ナトリウム原子、カリウム原子、セシウム原子、銀原子等が挙げられる。Ｂとして、好ましくは水素原子、リチウム原子、ナトリウム原子、カリウム原子、セシウム原子であり、さらに好ましくはリチウム原子、ナトリウム原子、カリウム原子であり、さらにより好ましくは水素原子、リチウム原子であり、特に好ましくは水素原子である。
本発明の化合物をリチウム二次電池用電解質として用いる場合には、Ｂとしてリチウムが用いられる。本発明の化合物を固体高分子型燃料電池に用いる場合は、実質的に全ての官能基が遊離酸の形である場合が好ましい。
上記において、本発明の実施の形態について説明を行なったが、上記に開示された本発明の実施の形態は、あくまで例示であって、本発明の範囲はこれらの実施の形態に限定されない。本発明の範囲は、特許請求の範囲によって示され、さらに特許請求の範囲の記載と均等の意味及び範囲内でのすべての変更を含むものである。 As a specific structural formula of the oxocarbon compound of the present invention, an oxocarbon compound represented by the following formula (3) in which fluorine is substituted at the para position of the oxocarbon group among the compounds represented by (a50): Can be mentioned.

Moreover, as an oxocarbon compound of the present invention, another specific structural formula includes an oxocarbon compound represented by the following formula (4) represented by (a53).

Examples of the oxocarbon compound in which R is a halogeno-substituted aryl group include those described above. These may be used in the form of a free acid having properties as a protonic acid, or the free acid is a monovalent metal. It may be substituted with atoms and neutralized. Examples of the monovalent metal atom include a lithium atom, a sodium atom, a potassium atom, a cesium atom, and a silver atom. B is preferably a hydrogen atom, lithium atom, sodium atom, potassium atom or cesium atom, more preferably a lithium atom, sodium atom or potassium atom, still more preferably a hydrogen atom or lithium atom, particularly preferably. Is a hydrogen atom.
When the compound of the present invention is used as an electrolyte for a lithium secondary battery, lithium is used as B. When the compound of the present invention is used in a polymer electrolyte fuel cell, it is preferable that substantially all functional groups are in the form of free acid.
While the embodiments of the present invention have been described above, the embodiments of the present invention disclosed above are merely examples, and the scope of the present invention is not limited to these embodiments. The scope of the present invention is defined by the terms of the claims, and further includes meanings equivalent to the description of the claims and all modifications within the scope.

EXAMPLES The present invention will be described in detail below with reference to examples, but the present invention is not limited to these examples.
Proton conductivity (σ) was measured as follows.
A platinum plate (width: 5.0 mm) is pressed against the surface of a strip-shaped film sample having a width of 1.0 cm so that the interval is 1.0 cm, and the sample is held in a constant temperature and humidity chamber. The AC impedance at ⁶ to 10 ⁻¹ Hz was measured and obtained from the following formula.
σ (S / cm) = 1 / (R × d)
(However, on the Cole-Cole plot, when the imaginary component of the complex impedance is 0, the real component of the complex impedance is R (Ω). D represents the film thickness (cm).)

Example 1
Poly (N-vinylpyrrolidone) (manufactured by Aldrich, hereinafter abbreviated as PVP) 0.50 g in a 50 ml flask was added 0.20 g (1.75 mmol) of 3,4-dihydroxy-3-cyclobutene-1,2-dione (A). , Manufactured by Tokyo Chemical Industry Co., Ltd.) and 5.0 ml of ion exchange water were added and stirred at room temperature for 30 minutes to obtain a uniform solution. This solution was spread on a petri dish and water was distilled off at 80 ° C. to obtain a film (a) having a thickness of 85 μm. [Amount of substance of oxocarbons (mmol)] / [weight of polymer compound (g) + weight of oxocarbons (g)] of (a) was 2.51 (mmol / g). Table 1 shows the proton conductivity of (a).

(Reference Example 1)
Synthesis of 3-Hydroxy-4-phenylcyclobut-3-ene-1,2-dione (I) According to the method described in Journal of Organic Chemistry, 1988, 53 (11), 2482, 3- (1- (Methylethoxy) -4-phenylcyclobut-3-ene-1,2-dione was prepared. Next, 0.63 g of this, 12 ml of THF, and 36 ml of 12 N hydrochloric acid were placed in a 100 ml flask and stirred at 100 ° C. for 5 hours. Then, after cooling to room temperature and washing the aqueous layer with chloroform, the aqueous layer was concentrated to obtain 0.24 g of 3-Hydroxy-4-phenylcyclobut-3-ene-1,2-dione (I). The structure was confirmed by ¹ H NMR and ¹³ C NMR.

(Example 2)
In a 50 ml flask, 0.38 g of polyethersulfone (Sumika Excel 5003P, manufactured by Sumitomo Chemical Co., Ltd., hereinafter abbreviated as PES) and 0.15 g (0.86 mmol) of the above (I) were added and dissolved by adding 3 ml of DMAc. did. This solution was cast on a glass plate and dried in an oven at 80 ° C. to obtain a uniform film (b) having a thickness of 180 μm. [Substance amount of oxocarbons (mmol)] / [weight of polymer compound (g) + weight of oxocarbons (g)] of (b) was 1.63 (mmol / g). The measurement results of the proton conductivity of (b) are shown in Table 2.

(Example 3)
A uniform film (c) having a thickness of 140 μm was obtained in the same manner as in Example 2, except that 0.28 g of PES and 0.22 g (1.26 mmol) of (I) were used. The [substance amount of oxocarbons (mmol)] / [weight of polymer compound (g) + weight of oxocarbons (g)] of (c) was 2.53 (mmol / g). The measurement results of proton conductivity of (c) are shown in Table 2.

Example 4
In Example 2, a uniform film (d) having a thickness of 175 μm was obtained in the same manner except that 0.28 g of polysulfone (manufactured by Aldrich) was used instead of PES. The [substance amount of oxocarbons (mmol)] / [weight of polymer compound (g) + weight of oxocarbons (g)] of (d) was 2.00 (mmol / g). Table 2 shows the measurement results of proton conductivity of (d).

(Comparative Example 1)
According to the method described in Example 1 of JP-A-10-21944, 4,4′-dihydroxydiphenylsulfone, 4,4′-dihydroxybiphenyl, and 4,4′-dichlorodiphenylsulfone are polycondensed and then obtained. The polycondensate was sulfonated to obtain polymer electrolyte 1. The equivalent of the sulfonic acid group in the polymer was 1.1 mmol / g.
Next, the polymer electrolyte 1 was dissolved in DMAc to make a uniform solution, spread on a petri dish, and DMAc was distilled off at 80 ° C. to obtain a film (e) having a thickness of 35 μm. Tables 1 and 2 show the proton conductivity of (e).

(Example 5)
Preparation of 4- (4-fluorophenyl) -3-Hydroxy-cyclobut-3-ene-1,2-dione (IV) and compositions According to the method described in Journal of Organic Chemistry, 1990, 55, 5359 4- (1-Methylethoxy) -3- (tri-n-butylstannyl) cyclobut-3-ene-1,2-dione (II) was produced.
Next, 92.0 mg (0.49 mmol) of copper (I) iodide, 1.17 g (5.24 mmol) of parafluoroiodobenzene, [(C ₆ H ₅ ) ₃ P] _{2 were} placed in a flask purged with an inert gas. After adding 0.22 g (0.29 mmol) of Pd (CH ₂ C ₆ H ₅ ) Cl and dissolving it in 6.0 ml of DMF, 2.00 g (4.8 mmol) of (II) synthesized above was added dropwise. After stirring for 4 hours, the reaction solution was diluted with 50 ml of diethyl ether and washed once with 50 ml of saturated aqueous ammonium chloride solution and 3 times with 50 ml of 10 wt% potassium fluoride aqueous solution. Ether and DMF were distilled off, and the resulting crude product was purified by column chromatography using silica gel as a filler and hexane: ether = 3: 1 (vol / vol) as a developing solvent. 4- (4-Fluorophenyl) -3- (1-methylethyoxy) -cyclobut-3-ene-1,2-dione (III) was obtained.
Next, 0.37 g (1.58 mmol) of (III) was dissolved in 0.1 ml of THF, 7.0 ml of 12N hydrochloric acid was added, and the mixture was stirred for 3 hours. Thereafter, the reaction solution was diluted by adding 10 ml of water, and washed once with 10 ml of CH ₂ Cl ₂ . Water in the aqueous layer was distilled off to obtain 0.179 g of 4- (4-fluorophenyl) -3-Hydroxy-cyclobut-3-ene-1,2-dione (IV). The structure was confirmed by ¹ H NMR (solvent in D ₂ O, 7.21 ppm (2H), 7.96 ppm (2H)), ¹⁹ F NMR (solvent in D ₂ O, -109.0 ppm). When the purity was confirmed by HPLC, it was 99% or more (peak area ratio).
Next, 41.0 mg of poly (N-vinylpyrrolidone) (manufactured by Aldrich, hereinafter abbreviated as PVP), 17.7 mg (0.0921 mmol) synthesized above (IV), ion-exchanged water, in a container having an internal volume of 20 ml 3.0 ml was added and stirred at room temperature for 30 minutes to obtain a uniform solution. This solution was spread on a petri dish and water was distilled off at 80 ° C. to obtain a film (f) having a thickness of 145 μm. The [substance amount of oxocarbons (mmol)] / [weight of polymer compound (g) + weight of oxocarbons (g)] of (f) was 1.57 (mmol / g). The proton conductivity of (f) is shown in Table 1.

(Example 6)
Preparation of 3-Hydroxy-4- (2,3,4,5,6-pentafluorophenyl) -cyclobut-3-ene-1,2-dione (VI) and composition Into a flask purged with inert gas, copper iodide was added. (I) 18.0 mg (0.095 mmol), pentafluoroiodobenzene 0.30 g (1.00 mmol), [(C ₆ H ₅ ) ₃ P] ₂ Pd (CH ₂ C ₆ H ₅ ) Cl 43.0 mg ( 0.057 mmol) was added and dissolved in 1.0 ml of DMF, and then 0.40 g (0.93 mmol) of (II) was added dropwise. After stirring for 4 hours, the reaction solution was diluted with 50 ml of diethyl ether and washed once with 50 ml of saturated aqueous ammonium chloride solution and 3 times with 50 ml of 10 wt% potassium fluoride aqueous solution. Ether and DMF were distilled off, and the resulting crude product was purified by column chromatography using silica gel as a filler and hexane: ether = 3: 1 (vol / vol) as a developing solvent. 4- (2,3,4,5,6-pentafluorophenyl) -3- (1-methylethyoxy) -cyclobut-3-ene-1,2-dione (V) was produced.
Next, 0.053 g (0.173 mmol) of (V) was dissolved in 0.1 ml of THF, 1.5 ml of 12N hydrochloric acid was added, and the mixture was stirred for 3 hours. Thereafter, the reaction solution was diluted by adding 10 ml of water, and washed once with 10 ml of CH ₂ Cl ₂ . Water in the aqueous layer was distilled off to obtain 23 mg of 3-Hydroxy-4- (2,3,4,5,6-pentafluorophenyl) -cyclo-3-ene-1,2-dione (VI). The structure was confirmed by ¹⁹ F NMR (D ₂ O solvent, KF standard (−125.3 ppm), chemical shift values: −138.3 ppm, −156.2 ppm, −165.7 ppm). ^No peak was observed in ¹ H NMR. When the purity was confirmed by HPLC, it was 99% or more (peak area ratio).
Next, 32.5 mg of poly (N-vinylpyrrolidone) (manufactured by Aldrich, hereinafter abbreviated as PVP), 23.0 mg (0.0871 mmol) synthesized above (VI), ion-exchanged water, in a container having an internal volume of 20 ml 3.0 ml was added and stirred at room temperature for 30 minutes to obtain a uniform solution. The solution was spread on a petri dish and water was distilled off at 80 ° C. to obtain a film (g) having a thickness of 158 μm. [Substance amount of oxocarbons (mmol)] / [weight of polymer compound (g) + weight of oxocarbons (g)] of (g) was 1.57 (mmol / g). The proton conductivity of (g) is shown in Table 1.

(Example 7)
In formula (1), X ¹ , X ² , Z, n, and R are the compounds B, polybenzimidazole, and NMP shown in Table 3, and are stirred to obtain a homogeneous solution. This solution is spread on a petri dish, and the solvent is volatilized and dried to obtain a film (h) of the composition. At this time, the compound B and the polybenzimidazole were mixed such that [the amount of oxocarbons (mmol)] / [weight of polymer electrolyte (g) + weight of oxocarbons (g)] in (h) was 0. When selected to be in the range of 0.05 to 8 mmol / g, it has a proton conductivity comparable to a polymer compound having a sulfonic acid group, and has chemical stability compared to a polymer compound having a sulfonic acid group. A film having excellent water resistance is preferably obtained.

(Example 8)
In Formula (1), X ¹ , X ² , Z, n, and R are the compounds C, polybenzimidazole, and NMP shown in Table 3 and placed in a flask to obtain a homogeneous solution. This solution is spread on a petri dish, and the solvent is volatilized and dried to obtain a film (i) of the composition. At this time, the compound C and the polybenzimidazole were mixed so that the [substance amount of oxocarbons (mmol)] / [weight of polymer electrolyte (g) + weight of oxocarbons (g)] of (i) was 0. When selected to be in the range of 0.05 to 8 mmol / g, it has a proton conductivity comparable to a polymer compound having a sulfonic acid group, and has chemical stability compared to a polymer compound having a sulfonic acid group. A film having excellent water resistance is preferably obtained.

Example 9
In Formula (1), X ¹ , X ² , Z, n, and R are the compounds D, PVP, and water shown in Table 3 and placed in a flask and stirred to obtain a uniform solution. This solution is spread on a petri dish, and the solvent is volatilized and dried to obtain a film (j) of the composition. At this time, the compound D and the PVP were mixed such that (j) [amount of oxocarbons (mmol)] / [weight of polymer electrolyte (g) + weight of oxocarbons (g)] was 0.05. When selected to be in the range of ˜8 mmol / g, it has proton conductivity comparable to a polymer compound having a sulfonic acid group, and has chemical stability and water resistance as compared with a polymer compound having a sulfonic acid group. A film having excellent properties is preferably obtained.

(Example 10)
In Formula (1), X ¹ , X ² , Z, n, and R are the compounds E, PVP, and water shown in Table 3 and placed in a flask and stirred to obtain a uniform solution. This solution is developed in a petri dish, and the solvent is volatilized and dried to obtain a film (k) of the composition. At this time, the compound E and PVP were mixed such that (substance of oxocarbons (mmol)) / [weight of polymer electrolyte (g) + weight of oxocarbons (g)] of (k) was 0.05. When selected to be in the range of ˜8 mmol / g, it has proton conductivity comparable to a polymer compound having a sulfonic acid group, and has chemical stability and water resistance as compared with a polymer compound having a sulfonic acid group. A film having excellent properties is preferably obtained.

(Example 11)
In Formula (1), X ¹ , X ² , Z, n, and R are compounds F and PES shown in Table 3, and a mixed solution of methylene chloride: methanol = 9: 1 (vol / vol), and stirred. Make a homogeneous solution. This solution is spread on a petri dish, and the solvent is volatilized and dried to obtain a film (1) of the composition. At this time, the compound F and the PES were mixed such that (l) [amount of oxocarbons (mmol)] / [weight of polymer electrolyte (g) + weight of oxocarbons (g)] of 0.05. When selected to be in the range of ˜8 mmol / g, it has proton conductivity comparable to a polymer compound having a sulfonic acid group, and has chemical stability and water resistance as compared with a polymer compound having a sulfonic acid group. A film having excellent properties is preferably obtained.

(Example 12)
In Formula (1), X ¹ , X ² , Z, n and R are a mixture of Compound G and PES shown in Table 3 and methylene chloride: methanol = 9: 1 (vol / vol) in a flask and stirred. Make a homogeneous solution. This solution is spread on a petri dish, and the solvent is volatilized and dried to obtain a film (m) of the composition. At this time, the compound G and the PES were mixed such that (m) [amount of oxocarbons (mmol)] / [weight of polymer electrolyte (g) + weight of oxocarbons (g)] of 0.05. When selected to be in the range of ˜8 mmol / g, it has proton conductivity comparable to a polymer compound having a sulfonic acid group, and has chemical stability and water resistance as compared with a polymer compound having a sulfonic acid group. A film having excellent properties is preferably obtained.

(Example 13)
In Formula (1), X ¹ , X ² , Z, n, and R are compounds H and PES shown in Table 3, and a mixed solution of methylene chloride: methanol = 9: 1 (vol / vol) is stirred in a flask. Make a homogeneous solution. This solution is spread on a petri dish, and the solvent is volatilized and dried to obtain a film (n) of the composition. At this time, the compound H and the PES were mixed so that (n) [amount of oxocarbons (mmol)] / [weight of polymer electrolyte (g) + weight of oxocarbons (g)] was 0.05. When selected to be in the range of ˜8 mmol / g, it has proton conductivity comparable to a polymer compound having a sulfonic acid group, and has chemical stability and water resistance as compared with a polymer compound having a sulfonic acid group. A film having excellent properties is preferably obtained.

（表１ 加湿下でのプロトン伝導度測定）

(Table 1 Measurement of proton conductivity under humidification)

（表２ 無加湿下でのプロトン伝導度測定）

(Table 2 Measurement of proton conductivity without humidification)

Claims (7)

It is a polymer composition containing an oxocarbon represented by the following formula (1) and a polymer compound , [amount of oxocarbons (mmol)] / [weight of polymer compound (g) + oxocarbon The polymer composition is characterized in that the weight (g) of the product is 0.05 to 8 mmol / g .

(In the formula, X ¹ and X ² represent —O— and Z represents —CO—. N represents the number of repetitions and represents an integer of 0 to 10. When there are a plurality of Z, Z may be the same as or different from each other, R is —OH, —SH, —NHR ′ ″, an optionally substituted alkyl group having 1 to 18 carbon atoms, An aryl group having 6 to 18 carbon atoms which may have a substituent or an aralkyl group having 7 to 16 carbon atoms which may have a substituent, R ′, R ″ and R ′ ″ are , Each independently represents a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, or an optionally substituted aryl group having 6 to 10 carbon atoms, and B represents a hydrogen atom. Or represents a monovalent metal atom.) 2. The polymer composition according to claim 1 , wherein n is an integer of 0 to 2. High molecular weight compounds are polyvinylpyrrolidones, poly (meth) acrylic acids, poly (meth) acrylic esters, poly (meth) acrylonitriles, polystyrenes, polyvinylpyridines, polyethylenes, polypropylenes, polybutenes, polyvinylidene Fluorides, polytetrafluoroethylenes, polyvinyl chlorides, polyoxyalkylenes, polysiloxanes, polyesters, polyimides, polyamides, polybenzoxazoles, polybenzimidazoles, polyarylene ethers, polyarylene 3. The polymer composition according to claim 1, wherein the polymer composition is at least one selected from the group consisting of a group, a polyarylene sulfide, a polyether ketone, a polyether sulfone, and a polyphosphazene. The polymer electrolyte which uses the polymer composition in any one of Claims 1-3 as an active ingredient. A polymer electrolyte membrane comprising the polymer electrolyte according to claim 4 . Battery, characterized in that it comprises at least one polymer electrolyte membrane according to polyelectrolytes and claim 5 of claim 4. Fuel cell characterized by having at least one polymer electrolyte membrane according to polyelectrolytes and claim 5 of claim 4.