JPWO2012114834A1 - 水性液状組成物、水性塗工液、機能性塗工膜、及び複合材料 - Google Patents
水性液状組成物、水性塗工液、機能性塗工膜、及び複合材料 Download PDFInfo
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- JPWO2012114834A1 JPWO2012114834A1 JP2012524944A JP2012524944A JPWO2012114834A1 JP WO2012114834 A1 JPWO2012114834 A1 JP WO2012114834A1 JP 2012524944 A JP2012524944 A JP 2012524944A JP 2012524944 A JP2012524944 A JP 2012524944A JP WO2012114834 A1 JPWO2012114834 A1 JP WO2012114834A1
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Abstract
Description
本発明の水性液状組成物には水系媒体が含有される。この水系媒体は、溶媒又は分散媒として機能する成分である。水系溶媒は、水のみであっても、水と有機溶媒との混合溶媒であってもよい。水は蒸留水が好ましいが、用途によっては通常の水道水であってもよい。
本発明の水性液状組成物に含有されるOH/NH2ポリマーとPBTCは、加熱されることによって反応し、架橋する。したがって、加熱前の状態においては、両者は均一に混合されていることが、反応効率的に好ましい。このため、OH/NH2ポリマーは、pH1〜14の水、又は水と有機溶媒とを含む水系媒体に、100℃以下で可溶であることが好ましい。
本発明の水性液状組成物にはPBTCが含有される。PBTCは、OH/NH2ポリマーの架橋剤として機能する。このため、本発明の水性液状組成物を塗工液として使用した際に、PBTCは形成される塗工膜の堅牢性向上に寄与する。また、架橋剤としての機能以外にも、形成される塗工膜の親水性、抗菌・防かび性、防臭性等の発現にも寄与しうる。PBTCは公知の物質であり、一般的にはキレート剤、スケール防止剤、洗浄剤、漂白剤、防腐剤、消毒剤、ドーパント等の用途に使用されている。なお、PBTCは、デイクエスト7000(サーモフォス社製)などの商品名で市場から入手することができる。
本発明の水性液状組成物には、ポリマー酸がさらに含有されることが好ましい。このポリマー酸は、カルボキシル基含有ビニルモノマーの単独重合体及び/又はカルボキシル基含有ビニルモノマーとカルボキシル基非含有ビニルモノマーとの共重合体である。このようなポリマー酸が含有されることで、形成される塗工膜の基材に対する密着性がさらに高められるとともに、形成される塗工膜の親水機能もさらに向上する。
本発明の水性液状組成物には、ポリアルキレングリコール及び/又はポリアルキレンオキサイドが含有されることが好ましい。ポリアルキレングリコールは、エチレンオキサイド、プロピレンオキサイド、ブチレンオキサイドなどのアルキレンオキサイドを開環重合することによって得られるノニオン性化合物である。また、ポリアルキレンオキサイドは、ポリアルキレングリコールのうち、より重合度の高い高分子量タイプのノニオン性化合物である。ポリアルキレングリコール及び/又はポリアルキレンオキサイドが含有されることで、形成される塗工膜により高い可撓性や親水性が付与される。
本発明の水性液状組成物には、導電性材料が含有されることが好ましい。導電性材料を含有させることにより、電気的な接触性が向上した塗工膜を形成することができる。このようにして形成された塗工膜は、リチウム二次電池やキャパシタなどの蓄電装置に用いられる集電体の塗工膜として好適である。すなわち、良好な導電性を有する塗工膜を形成することができるので、電極層の内部抵抗を低減することができるとともに、容量密度を高くすることができる。
本発明の水性液状組成物は、適切なOH/NH2ポリマー、ポリマー酸、ポリアルキレングリコール、及びポリアルキレンオキサイドなどを選択して含有させることで、環境負荷が少なく、優れた機能性を有する水性塗工液として用いることができる。具体的には、本発明の水性液状組成物は、塗料、インク、磁性体、セラミックス、蓄電装置、接着剤、電子材料、液晶カラーフィルター、医薬品、化粧品、香料など様々な分野での利用が期待できる。例えば、カーボンブラックなどの導電性材料を含有させることで、リチウムイオン二次電池やキャパシタなどの蓄電装置の集電体の表面に形成される導電性塗工膜を形成するための導電性塗工液として使用することができる。
本発明の水性塗工液は、前述の水性液状組成物を含有するものである。なお、前述の水性液状組成物のみをそのまま塗工液として用いることもできる。また、用途に応じて適切な希釈倍率となるように水系媒体で希釈して用いることもできる。
<2塩基酸>シュウ酸、マロン酸、コハク酸、メチルコハク酸、グルタル酸、メチルグルタル酸、アジピン酸、ピメリン酸、スベリン酸、アゼライン酸、セバシン酸、マレイン酸、メチルマレイン酸、フマル酸、メチルフマル酸、イタコン酸、ムコン酸、シトラコン酸、グルタコン酸、アセチレンジカルボン酸、酒石酸、リンゴ酸、スピクリスポール酸、グルタミン酸、グルタチオン、アスパラギン酸、シスチン、アセチルシスチン、ジグリコール酸、イミノジ酢酸、ヒドロキシエチルイミノジ酢酸、チオジグリコール酸、チオニルジグリコール酸、スルホニルジグリコール酸、ポリエチレンオキシドジグリコール酸(PEG酸)、ピリジンジカルボン酸、ピラジンジカルボン酸、エポキシコハク酸、フタル酸、イソフタル酸、テレフタル酸、テトラクロルフタル酸、ナフタレンジカルボン酸、テトラヒドロフタル酸、メチルテトラヒドロフタル酸、シクロヘキサンジカルボン酸、ジフェニルスルホンジカルボン酸、ジフェニルメタンジカルボン酸
本発明の機能性塗工膜は、前述の水性塗工液を被塗工物(基材)の表面に塗布して形成した塗布膜を加熱乾燥することにより形成される。水性塗工液の塗布量は特に制限されないが、形成される機能性塗工膜の厚さが、通常0.05〜100μm、好ましくは0.1〜10μm、さらに好ましくは0.1〜5μm、特に好ましくは0.1〜2μmとなる量であればよい。基材としては、アルミニウムや銅などの金属、ガラス、天然樹脂、合成樹脂、セラミックス、木材、紙、繊維、織布、不織布、皮革などが挙げられる。なかでも、アルミニウム箔や銅箔などの蓄電装置用集電体が好ましい。
本発明の水性液状組成物及び水性塗工液は、導電性材料を含む場合においては、二次電池やキャパシタなどの蓄電装置用の電極板を構成する導電性塗工膜の形成材料として好適である。なお、集電体10の表面に塗布した水性液状組成物又は水性塗工液を加熱乾燥することで、図1に示すような、集電体10と、この集電体10の表面に配設された導電性塗工膜12とを備えた電極板用部材14を得ることができる。導電性塗工膜12の厚さは、通常0.1〜10μm、好ましくは0.1〜5μm、さらに好ましくは0.1〜2μmである。形成した導電性塗工膜12の上に、電池用正極電極層、電池用負極電極層、キャパシタ用正極電極層、キャパシタ用負極電極層、又は分極性電極層などの活物質層16を形成することによって、図1に示すような、電極層−集電体間の抵抗が小さく、環境負荷の少ない蓄電装置用の電極板20を製造することができる。
本発明の水性液状組成物及び水性塗工液は、ガラスなどの基材の表面に設ける親水性塗工膜の形成材料として好適である。親水性塗工膜を形成することで、防曇性が付与される。親水性塗工膜の厚さは、通常0.1〜10μm、好ましくは0.1〜5μm、さらに好ましくは0.1〜2μmである。
本発明の複合材料は、基材と、この基材上に一体的に配設された前述の機能性塗工膜とを備える。本発明の複合材料は、親水性、導電性、抗菌・防臭性、風合い、防曇性、紙力、染色性、耐水性、防汚染性などに優れた材料である。なお、本発明の複合材料は、基材上に前述の水性液状組成物又は水性塗工液を塗布して形成された塗布膜を加熱乾燥することなどにより製造することができる。
各種水性液状組成物の組成を表1−1及び1−2に示す。なお、ヒドロキシプロピルキトサンを「HPC」、ヒドロキシブチルキトサンを「HBC」、グリセリル化キトサンを「GLYC」、ホスホノブタントリカルボン酸を「PBTC」、イソプロピルアルコールを「IPA」と略した。
イオン交換水81部にキトサン(脱アセチル化度85%、重量平均分子量10万)5部と50%PBTC水溶液(サーモフォス社製、デイクエスト7000)14部を加えた後、室温で4時間撹拌溶解し、100部の水性液状組成物を調製した。
表1−1及び1−2に示す組成としたこと以外は、前述の例1−1と同様にして水性液状組成物を調製した。
イオン交換水65部にキトサン(脱アセチル化度85%、重量平均分子量10万)10部とポリアクリル酸水溶液(東亞合成社製、ジュリマーAC−10L(固形分40%、MW25,000))25部を加えた後、室温で24時間撹拌した。しかしながら、キトサンは溶解せず、均一な水性液状組成物を得ることはできなかった。
(実施例1)
(1)導電性塗工液
アセチレンブラック10部と例1−1の水性液状組成物90部を配合し、プラネタリーミキサーを使用して、回転数60rpmで120分間撹拌混合させて導電性塗工液を調製した。
調製した導電性塗工液を、厚さ20μmのアルミニウム箔からなる集電体の片面に、コンマロールコーターを用いて塗布した。110℃のオーブンで2分間加熱乾燥し、さらに180℃のオーブンで2分間加熱乾燥して、膜厚1μmの導電性塗工膜を集電体の片面上に形成した。
EC(エチレンカーボネート):PC(プロピレンカーボネート):DME(ジメトキシエタン)=1:1:2(体積比)で配合した混合溶媒に、支持塩として1モルのLiPF6を溶解した溶液を調製した。導電性塗工膜を70℃の溶液に72時間浸漬した後、状態を観察した。導電性塗工膜に変化のないものを溶解・膨潤性「良」と評価した。また、導電性塗工膜層が剥離又は膨潤したものを溶解・膨潤性「不良」と評価した。結果を表2に示す。
コンマロールコーターを用いて導電性塗工液をPETフィルム上に塗布した後、180℃のオーブンで5分間乾燥処理し、導電性塗工膜(乾燥膜厚4μm)を形成した。JIS K 7194に従い、形成した導電性塗工膜の表面抵抗率を四探針法により測定した。結果を表2に示す。なお、四探針法による測定には、三菱化学アナリテック社製のロレスターGP、MCP−T610を使用し、25℃、相対湿度60%の条件下で実施した。
例1−1の水性液状組成物に代えて、表2に示す水性液状組成物を使用したこと以外は、前述の実施例1と同様にして導電性塗工液を調製した。また、実施例1と同様にして溶解・膨潤性の評価及び表面抵抗率の測定を行った。結果を表2に示す。なお、比較例2ではポリビニリデンフルオライドの5%NMP溶液(PVDF溶液)を用いた。
(実施例20)
(1)正極電極板
実施例1の導電性塗工液を、厚さ20μmのアルミニウム箔からなる集電体の片面に、コンマロールコーターを用いて塗布した。110℃のオーブンで2分間加熱乾燥し、さらに180℃のオーブンで2分間加熱乾燥して、膜厚が1μmの導電性塗工膜を集電体の片面上に形成した。
実施例1の導電性塗工液を、銅箔集電体の片面に、コンマロールコーターを用いて塗布した。110℃のオーブンで2分間加熱乾燥し、さらに180℃のオーブンで2分間加熱乾燥して、膜厚が1μmの導電性塗工膜を集電体の片面上に形成した。
正極電極板と負極電極板を、三次元空孔構造(海綿状)を有する正極電極板より幅広のポリオレフィン系(ポリプロピレン、ポリエチレン、又はこれらの共重合体)の多孔性フィルムからなるセパレータを介して渦巻き状に捲回して電極体を作製した。作製した電極体を、負極端子を兼ねた有底円筒状のステンレス容器内に挿入し、AAサイズで定格容量500mAhの電池を組み立てた。この電池にEC(エチレンカーボネート):PC(プロピレンカーボネート):DME(ジメトキシエタン)=1:1:2(体積比)で全量1リットルになるように調製した混合溶媒に、支持塩として1モルのLiPF6を溶解したものを電解液として注液した。
充放電測定装置を使用し、25℃の温度条件で電池の充放電特性を測定した。20セルずつ、充電電流0.2CAの電流値で、充電方向から電池電圧4.1Vになるまで充電し、10分間の休止の後、同一電流で2.75Vになるまで放電し、10分間の休止の後、以下同一条件で100サイクルの充放電を繰り返して充放電特性を測定した。1サイクル目の充放電容量値を100とした場合における、100回目の充放電容量値(充放電容量維持率)は99%であった。
実施例1の導電性塗工液に代えて、表3に示す導電性塗工液を使用したこと以外は、前述の実施例20と同様にして電池を作製した。また、実施例20と同様にして充放電容量維持率を測定した。結果を表3に示す。
(実施例26)
実施例1の導電性塗工液を、厚さ20μmのアルミニウム箔からなる集電体の片面に、コンマロールコーターを用いて塗布した。110℃のオーブンで2分加熱乾燥し、さらに180℃のオーブンで2分間加熱乾燥して、膜厚が0.5μmの導電性塗工膜を集電体の片面上に形成した。
実施例1の導電性塗工液に代えて、表4に示す導電性塗工液を用いたこと以外は、前述の実施例26と同様にしてキャパシタを得た。また、得られたキャパシタの静電容量及び内部抵抗を測定した。測定結果を表4に示す。
実施例1の導電性塗工液に代えて、表4に示す導電性塗工液を用いたこと以外は、前述の実施例26と同様にしてキャパシタを得た。得られたキャパシタの静電容量及び内部抵抗を測定し、実施例26〜31のキャパシタを評価する基準とした。
A:比較例4よりも静電容量が20%以上大きい。
B:比較例4よりも静電容量が10%以上20%未満大きい。
C:比較例4と静電容量が同等以下である。
A:比較例4よりも内部抵抗が20%以上小さい。
B:比較例4よりも内部抵抗が10%以上20%未満小さい。
C:比較例4と内部抵抗が同等以下である。
各種親水性塗工液の組成を表5−1及び5−2に示す。なお、ホスホノブタントリカルボン酸を「PBTC」、ブタンテトラカルボン酸を「BTC」、ポリアクリル酸を「PAA」、ポリマレイン酸を「PMA」、ポリビニルアルコールを「PVA」、ポリエチレングリコールを「PEG」、ポリエチレンオキサイドを「PEO」と略した。
イオン交換水79部にキトサン(脱アセチル化度85%、重量平均分子量10万)5部を分散させて分散液を得た。得られた分散液に50%PBTC水溶液(サーモフォス社製、デイクエスト7000)16部を加えた後、室温で4時間撹拌して100部の親水性塗工液を調製した。
イオン交換水64部にキトサン(脱アセチル化度85%、重量平均分子量6万)6部を分散させて分散液を得た。得られた分散液に50%PBTC水溶液(サーモフォス社製、デイクエスト7000)20部を加えた後、室温で4時間撹拌した。次に、撹拌下、ポリアクリル酸水溶液(東亞合成社製、ジュリマーAC−10L(固形分40%、MW25,000))10部を加えた後、室温で2時間撹拌して100部の親水性塗工液を調製した。
表5−1及び5−2に示す組成としたこと以外は、前述の実施例32及び33と同様にして親水性塗工液を調製した。
イオン交換水90部とグリセリル化キトサン10部とを混合し、室温で4時間撹拌溶解して親水性塗工液を調製した。
イオン交換水37.5部に、10%PVA水溶液(クラレ社製、クラレポバールPVA117)50部を添加した後、撹拌下、ポリアクリル酸水溶液(東亞合成社製、ジュリマーAC−10L(固形分40%、Mw25,000))12.5部を添加した。室温で2時間撹拌して、100部の親水性塗工液を調製した。
表5−1及び5−2に示す組成としたこと以外は、前述の実施例32と同様にして親水性塗工液を調製した。
(1)親水性塗工膜の形成
板厚1mmのガラス板(100×100mm)表面に、バーコーター(No.3)を用いて実施例32〜47及び比較例5〜8の親水性塗工液を、1g/m2の乾燥膜量となるように塗布した。次いで、親水性塗工液を塗布したガラス板を表6に示す条件で加熱乾燥し、約0.7μmの親水性塗工膜がガラス板上に形成された供試材を得た。
供試材を水道水で1時間流水洗浄(流量1L/分)した後、80℃で1時間送風乾燥した。この流水洗浄と80℃乾燥の処理を1サイクルとし、合計10サイクルの繰り返し洗浄を行った。
水平状態にした供試材の表面に2μlの純水を滴下した。JIS K2396に準拠し、接触角計(協和界面科学社製、DropMaster100)を使用して水滴の接触角を測定した。なお、接触角の測定は、供試材の洗浄前と、10サイクルの繰り返し洗浄後の両方で行った。
測定した接触角から、以下の基準に従って親水性塗工膜の洗浄前後の親水性を評価した。結果を表6に示す。
5:接触角が10°未満。
4:接触角が10°以上20°未満。
3:接触角が20°以上30°未満。
2:接触角が30°以上40°未満。
1:接触角が40°以上50°未満。
0:接触角が50°以上。
12:導電性塗工膜
14:電極板用部材
16:活物質層
20:電極板
Claims (24)
- 水を含む水系媒体と、水酸基及び/又はアミノ基を有するポリマーと、ホスホノブタントリカルボン酸とを含有する水性液状組成物。
- ポリマー酸をさらに含有し、
前記ポリマー酸が、カルボキシル基含有ビニルモノマーの単独重合体及び/又はカルボキシル基含有ビニルモノマーとカルボキシル基非含有ビニルモノマーとの共重合体である請求項1に記載の水性液状組成物。 - 前記ポリマー酸が、ポリアクリル酸、ポリマレイン酸、及びポリイタコン酸からなる群より選択される少なくとも一種である請求項2に記載の水性液状組成物。
- ポリアルキレングリコール及び/又はポリアルキレンオキサイドをさらに含有する請求項1〜3のいずれか一項に記載の水性液状組成物。
- 前記ポリマーが、多糖、ポリアミノ酸、ポリビニルアルコール、ポリアリルアミン、ポリビニルアミン、ポリアミジン、ポリエチレンイミン、及びこれらの誘導体からなる群より選択される少なくとも一種である請求項1〜4のいずれか一項に記載の水性液状組成物。
- 前記多糖が、アルギン酸、澱粉、セルロース、キチン、キトサン、ペクチン、及びこれらの誘導体からなる群より選択される少なくとも一種である請求項5に記載の水性液状組成物。
- 前記ポリアミノ酸が、ポリリジン、ポリオルニチン、ポリアルギニン、ポリヒスチジン、プロタミン、ゼラチン、及びコラーゲンからなる群より選択される少なくとも一種である請求項5に記載の水性液状組成物。
- 前記ポリマー(A)と前記ホスホノブタントリカルボン酸(B)との質量比が、A/B=1/5〜5/1である請求項1〜5のいずれか一項に記載の水性液状組成物。
- 前記ポリマーの重量平均分子量が、5,000〜200万である請求項1〜8のいずれか一項に記載の水性液状組成物。
- 前記ポリマーと前記ホスホノブタントリカルボン酸との合計の固形分濃度が、0.1〜40質量%である請求項1〜9のいずれか一項に記載の水性液状組成物。
- 導電性材料をさらに含有する請求項1〜10のいずれか一項に記載の水性液状組成物。
- 前記導電性材料が、アセチレンブラック、ケッチェンブラック、黒鉛、ファーネスブラック、単層又は多層カーボンナノファイバー、及び単層又は多層カーボンナノチューブからなる群より選択される少なくとも一種である請求項11に記載の水性液状組成物。
- 請求項1〜12のいずれか一項に記載の水性液状組成物を含む水性塗工液。
- 請求項13に記載の水性塗工液により形成される機能性塗工膜。
- JIS K7194で測定した表面抵抗率が3,000Ω/□以下である請求項14に記載の機能性塗工膜。
- 請求項13に記載の水性塗工液を80℃以上に加熱する工程を含む機能性塗工膜の形成方法。
- 基材と、前記基材上に一体的に配設された請求項14又は15に記載の機能性塗工膜と、を備えた複合材料。
- 前記基材が、金属、ガラス、天然樹脂、合成樹脂、セラミックス、木材、紙、繊維、不織布、織布、及び皮革からなる群より選択される少なくとも一種である請求項17に記載の複合材料。
- 前記基材が、アルミニウム、銅、ニッケル、及びステンレスからなる群より選択される少なくとも一種である請求項17に記載の複合材料。
- 集電体と、前記集電体の表面に配設された導電性塗工膜と、を備え、
前記導電性塗工膜が、前記集電体の表面に塗布された請求項11又は12に記載の水性液状組成物が加熱処理されて形成されたものである電極板用部材。 - 前記集電体が、非水電解液二次電池用、電気二重層キャパシタ用、又はリチウムイオンキャパシタ用の集電体である請求項20に記載の電極板用部材。
- 請求項20又は21に記載の電極板用部材と、前記導電性塗工膜の表面に配設された活物質層と、を備える電極板。
- 請求項22に記載の電極板を備える蓄電装置。
- 非水電解液二次電池、電気二重層キャパシタ、又はリチウムイオンキャパシタである請求項23に記載の蓄電装置。
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