JP5763563B2 - 表面改質方法及び表面改質弾性体 - Google Patents
表面改質方法及び表面改質弾性体 Download PDFInfo
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- JP5763563B2 JP5763563B2 JP2012017259A JP2012017259A JP5763563B2 JP 5763563 B2 JP5763563 B2 JP 5763563B2 JP 2012017259 A JP2012017259 A JP 2012017259A JP 2012017259 A JP2012017259 A JP 2012017259A JP 5763563 B2 JP5763563 B2 JP 5763563B2
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- modification method
- surface modification
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Description
本発明は、上記表面改質方法により得られる水存在下又は乾燥状態での摺動性、低摩擦又は水の低抵抗が要求される表面改質弾性体に関する。
本発明は、三次元形状の固体表面の少なくとも一部を上記表面改質方法で改質した表面改質弾性体に関する。ここで、上記表面改質弾性体は、ポリマーブラシであることが好ましい。
本発明は更に、上記表面改質方法により改質されたタイヤの溝表面を少なくとも一部に有するタイヤに関する。
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12−heneicosafluorododecyl acrylate(H2C=CHCO2CH2CH2(CF2)9CF3)、3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10−Heptadecafluorodecyl acrylate(H2C=CHCO2CH2CH2(CF2)7CF3)、3−(perfluorobutyl)−2−hydroxypropyl acrylate(F(CF2)4CH2CH(OH)CH2OCOCH=CH2)、3−perfluorohexyl−2−hydroxypropyl acrylate(F(CF2)6CH2CH(OH)CH2OCOCH=CH2)、3−(perfluoro−3−methylbutyl)−2−hydroxypropyl acrylate((CF3)2CF(CF2)2CH2CH(OH)CH2OCOCH=CH2)、3−(perfluoro−5−methylhexyl)−2−hydroxypropyl acrylate((CF3)2CF(CF2)4CH2CH(OH)CH2OCOCH=CH2)が好ましい。これらは単独又は2種以上を併用できる。
エルゴカルシフェロール、コレカルシフェロール、1,2,5−ジヒドロキシ−コレカルシフェロールなどのビタミンD類、それらの誘導体及びそれらの塩;α−トコフェロール、β−トコフェロール、γ−トコフェロール、δ−トコフェロール、α−トコトリエノール、β−トコトリエノール、γ−トコトリエノール、δ−トコトリエノール、酢酸トコフェロール、ニコチン酸トコフェロールなどのビタミンE類、それらの誘導体及びそれらの塩;トロロックス、その誘導体及びそれらの塩;ジヒドロキシトルエン、ブチルヒドロキシトルエン、ブチルヒドロキシアニソール、ジブチルヒドロキシトルエン、α−リポ酸、デヒドロリポ酸、グルタチオン、その誘導体及びそれらの塩;尿酸、エリソルビン酸、エリソルビン酸ナトリウムなどのエリソルビン酸、その誘導体及びそれらの塩;没食子酸、没食子酸プロピルなどの没食子酸、その誘導体及びそれらの塩;ルチン、α−グリコシル−ルチンなどのルチン、その誘導体及びそれらの塩;トリプトファン、その誘導体及びそれらの塩;ヒスチジン、その誘導体及びそれらの塩;N−アセチルシステイン、N−アセチルホモシステイン、N−オクタノイルシステイン、N−アセチルシステインメチルエステルなどのシステイン誘導体及びそれらの塩;N,N’−ジアセチルシスチンジメチルエステル、N,N’−ジオクタノイルシスチンジメチルエステル、N,N’−ジオクタノイルホモシスチンジメチルエステルなどのシスチン誘導体及びそれらの塩;カルノシン、その誘導体及びそれらの塩;ホモカルノシン、その誘導体及びそれらの塩;アンセリン、その誘導体及びそれらの塩;カルシニン、その誘導体及びそれらの塩;ヒスチジン及び/又はトリプトファン及び/又はヒスタミンを含むジペプチド又はトリペプチド誘導体及びそれらの塩;フラバノン、フラボン、アントシアニン、アントシアニジン、フラボノール、クエルセチン、ケルシトリン、ミリセチン、フィセチン、ハマメリタンニン、カテキン、エピカテキン、ガロカテキン、エピガロカテキン、エピカテキンガレート、エピガロカテキンガレートなどのフラボノイド類;タンニン酸、コーヒー酸、フェルラ酸、プロトカテク酸、カルコン、オリザノール、カルノソール、セサモール、セサミン、セサモリン、ジンゲロン、クルクミン、テトラヒドロクルクミン、クロバミド、デオキシクロバミド、ショウガオール、カプサイシン、バニリルアミド、エラグ酸、ブロムフェノール、フラボグラシン、メラノイジン、リボフラビン、リボフラビン酪酸エステル、フラビンモノヌクレオチド、フラビンアデニンヌクレオチド、ユビキノン、ユビキノール、マンニトール、ビリルビン、コレステロール、エブセレン、セレノメチオニン、セルロプラスミン、トランスフェリン、ラクトフェリン、アルブミン、スーパーオキシドジスムターゼ、カタラーゼ、グルタチオンペルオキシダーゼ、メタロチオネイン、O−ホスホノ−ピリドキシリデンローダミンなどが挙げられる。これらは単独又は2種以上を併用して用いてもよい。
また、ラジカル重合性モノマーの使用量は、形成するポリマー鎖の長さ、その鎖により発揮される性能などにより、適宜設定すればよい。更に、還元剤、抗酸化物質の使用量も系内の酸素の補足などの点から、適宜設定すればよい。
図2〜3において、中央縦溝3a(溝深さD1)、ショルダー縦溝3b(溝深さD2)は、タイヤ周方向に直線状にのびるストレート溝で構成される。このようなストレート溝は、排水抵抗を小さくし、直進走行時に高い排水性能を発揮しうる。
イソプレンユニットを含むクロロブチルゴム(不飽和度:1〜2%)をトリアジンで架橋した加硫ゴム(180℃で10分加硫)をベンゾフェノンの3wt%アセトン溶液に浸漬して、加硫ゴム表面にベンゾフェノンを吸着させた。365nmの波長を持つLEDライトを10分照射して、ベンゾフェノンを固定させた。その後、加硫ゴムを取り出し乾燥した。
乾燥した加硫ゴムの表面に3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10−Heptadecafluorodecyl acrylate(シグマアルドリッチ製)の液を塗布し、表面にガラス板を被せた。そのガラス板の上から365nmの波長を持つLEDライトを2時間照射してラジカル重合を行ってゴム表面にポリマー鎖を成長させ、表面改質弾性体(ポリマーブラシ)を得た。
3−perfluorohexyl−2−hydroxypropyl acrylate(F(CF2)6CH2CH(OH)CH2OCOCH=CH2:ダイキン工業製R1633)を使用した以外は実施例1と同様にして表面改質弾性体(ポリマーブラシ)を作製した。
3−(perfluoro−3−methylbutyl)−2−hydroxypropyl acrylate((CF3)2CF(CF2)2CH2CH(OH)CH2OCOCH=CH2:FluoroChem社製)を使用した以外は実施例1と同様にして表面改質弾性体(ポリマーブラシ)を作製した。
3−(perfluoro−5−methylhexyl)−2−hydroxypropyl acrylate((CF3)2CF(CF2)4CH2CH(OH)CH2OCOCH=CH2:FluoroChem社製)を使用した以外は実施例1と同様にして表面改質弾性体(ポリマーブラシ)を作製した。
イソプレンユニットを含むクロロブチルゴム(不飽和度:1〜2%)をトリアジンで架橋した加硫ゴム(180℃で10分加硫)をベンゾフェノンの3wt%アセトン溶液に浸漬して、加硫ゴム表面にベンゾフェノンを吸着させた。365nmの波長を持つLEDライトを10分照射して、ベンゾフェノンを固定させた。その後、加硫ゴムを取り出し乾燥した。
乾燥した加硫ゴムの表面に3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10−Heptadecafluorodecyl acrylate(シグマアルドリッチ製)の液に浸漬し、その上にリボフラビン水溶液(濃度0.0093mmol/L)を入れた。水溶液はモノマー液と混ざらず、かつ水溶液はモノマー液のより比重が軽いことから上層に分離した状態になった。そして上から365nmの波長を持つLEDライトを2時間照射してラジカル重合を行ってゴム表面にポリマー鎖を成長させ、表面改質弾性体(ポリマーブラシ)を得た。
イソプレンユニットを含むクロロブチルゴム(不飽和度:1〜2%)をトリアジンで架橋した加硫ゴム(180℃で10分加硫)そのものを用いた。
(ポリマー鎖の長さ)
加硫ゴム表面に形成されたポリマー鎖の長さは、ポリマー鎖が形成された改質ゴム断面を、SEMを使用し、加速電圧15kV、1000倍で測定した。撮影されたポリマー層の厚みをポリマー鎖の長さとした。
表面改質弾性体の表面の静摩擦係数、動摩擦係数、及びそれぞれに水を200μL滴下したサンプル表面の静摩擦係数、動摩擦係数を、ASTM D1894に規定された方法に準拠して測定した。また、サンプルは、ホウケイ酸ガラスと接触させて、ホウケイ酸ガラスとの間の摩擦力を測定した。なお、摩擦係数の測定のための荷重は200g、引張速度は600mm/min、ロード距離は10cmの条件で測定した。装置は、ヘイドンtype14(新東科学(株)製)を使用した。
静摩擦係数、動摩擦係数が大きく下がり、良好な摺動性が得られることが明らかとなった。また、表面のみ改質したものであるため、シール性は、比較例1と同等であった。
11a、11b、11c 環状突起部
13 底面部の表面
2 トレッド部
3a 中央縦溝
3b ショルダー縦溝
5 細溝
6 中間傾斜溝
7 継ぎ溝
8、8a、8b ショルダー横溝
Claims (16)
- 加硫ゴム又は熱可塑性エラストマーを改質対象物とする表面改質方法であって、
前記改質対象物の表面に300〜400nmのLED光を照射し、前記表面上の光増感剤から重合開始点を形成する工程1と、
前記重合開始点を起点にして、ラジカル重合性モノマーを300nm〜400nmのLED光を照射してラジカル重合させ、前記改質対象物の表面にポリマー鎖を成長させる工程2とを含み、
前記ラジカル重合性モノマーが、フルオロ基含有モノマーである表面改質方法。 - 前記工程2は、前記重合開始点を起点にして、還元剤又は抗酸化物質が添加されたラジカル重合性モノマーを300〜400nmのLED光を照射してラジカル重合させ、前記改質対象物の表面にポリマー鎖を成長させるものである請求項1記載の表面改質方法。
- 前記加硫ゴム又は熱可塑性エラストマーが二重結合に隣接する炭素原子であるアリル位の炭素原子を有する請求項1又は2記載の表面改質方法。
- 前記還元剤又は抗酸化物質は、リボフラビン、アスコルビン酸、α−トコフェロール、β−カロテン及び尿酸からなる群より選択される少なくとも1種である請求項1〜4のいずれかに記載の表面改質方法。
- 前記LED光の照射時又は照射前に反応容器及び反応液に不活性ガスを導入し、不活性ガス雰囲気に置換して重合させる請求項1〜5のいずれかに記載の表面改質方法。
- 前記フルオロ基含有モノマーは、フルオロアルキル基含有モノマーである請求項1〜6のいずれかに記載の表面改質方法。
- 前記フルオロアルキル基含有モノマーは、3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12−heneicosafluorododecyl acrylate(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12−ヘネイコサフルオロドデシル アクリレート、H2C=CHCO2CH2CH2(CF2)9CF3)、3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10−Heptadecafluorodecyl acrylate(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10−ヘプタデカフルオロデシル アクリレート、H2C=CHCO2CH2CH2(CF2)7CF3)、3−(perfluorobutyl)−2−hydroxypropyl acrylate(3−(パーフルオロブチル)−2−ヒドロキシプロピル アクリレート、F(CF2)4CH2CH(OH)CH2OCOCH=CH2)、3−perfluorohexyl−2−hydroxypropyl acrylate(3−パーフルオロヘキシル−2−ヒドロキシプロピル アクリレート、F(CF2)6CH2CH(OH)CH2OCOCH=CH2)、3−(perfluoro−3−methylbutyl)−2−hydroxypropyl acrylate(3−(パーフルオロ−3−メチルブチル)−2−ヒドロキシプロピル アクリレート、(CF3)2CF(CF2)2CH2CH(OH)CH2OCOCH=CH2)、及び3−(perfluoro−5−methylhexyl)−2−hydroxypropyl acrylate(3−(パーフルオロ−5−メチルヘキシル)−2−ヒドロキシプロピル アクリレート、(CF3)2CF(CF2)4CH2CH(OH)CH2OCOCH=CH2)からなる群より選択される少なくとも1種である請求項7記載の表面改質方法。
- 前記フルオロアルキル基含有モノマーは、下記式(3)、(4)、(5)又は(6)で表される化合物である請求項7記載の表面改質方法。
- 前記フルオロ基含有モノマーは、フルオロアルキレンオキシド基又はフルオロベンジル基含有モノマーである請求項1〜6のいずれかに記載の表面改質方法。
- 前記フルオロ基含有モノマーは、[1H,1H−perfluoro(2,5−dimethyl−3,6−dioxanonanoyl)]acrylate([1H,1H−パーフルオロ(2,5−ジメチル−3,6−ジオキサノナノイル)]アクリレート)、[1H,1H−perfluoro(2,5−dimethyl−3,6−dioxanonanoyl)]methacrylate([1H,1H−パーフルオロ(2,5−ジメチル−3,6−ジオキサノナノイル)]メタクリレート)、pentafluorobenzyl acrylate(ペンタフルオロベンジル アクリレート)、pentafluorobenzyl methacrylate(ペンタフルオロベンジル メタクリレート)、及び2,3,5,6−tetrafluorophenyl methacrylate(2,3,5,6−テトラフルオロフェニル メタクリレート)からなる群より選択される少なくとも1種である請求項1〜6のいずれかに記載の表面改質方法。
- 前記ラジカル重合性モノマー(液体)又はその溶液が重合禁止剤を含むもので、該重合禁止剤の存在下で重合させる請求項1〜11のいずれかに記載の表面改質方法。
- 前記重合禁止剤が4−メチルフェノールである請求項12記載の表面改質方法。
- 前記ポリマー鎖の長さは、10〜50000nmである請求項1〜13のいずれかに記載の表面改質方法。
- 請求項1〜14のいずれかに記載の表面改質方法により改質された表面を少なくとも一部に有する注射器用ガスケット。
- 請求項1〜14のいずれかに記載の表面改質方法により改質されたタイヤの溝表面を少なくとも一部に有するタイヤ。
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