JP2013095690A - 複合粒子および硬化性組成物 - Google Patents
複合粒子および硬化性組成物 Download PDFInfo
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- JP2013095690A JP2013095690A JP2011239051A JP2011239051A JP2013095690A JP 2013095690 A JP2013095690 A JP 2013095690A JP 2011239051 A JP2011239051 A JP 2011239051A JP 2011239051 A JP2011239051 A JP 2011239051A JP 2013095690 A JP2013095690 A JP 2013095690A
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- monomer
- polymerization
- bis
- methacrylate
- polymer chain
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Abstract
【解決手段】粒子表面2aに、高分子鎖3がグラフト結合され、高分子鎖3が、2種類のモノマーを共重合させたコポリマーを有し、2種類のモノマーは、当該複合粒子1が分散される重合性モノマーに対する親和性が異なるものであり、高分子鎖3のモノマー組成は、該高分子鎖3の粒子表面2aに結合している基端部側では、前記重合性モノマーに対する親和性の低いモノマーのブロック4とし、前記高分子鎖3の先端部側では、親和性の高いモノマーのブロック5としている。
【選択図】図1
Description
前記高分子鎖のモノマー組成は、該高分子鎖の前記粒子の表面に結合している基端部側では、前記重合性モノマーに対する親和性の低いモノマーが前記親和性の高いモノマーに比べて高く、前記高分子鎖の先端部側では、前記親和性の高いモノマーが前記親和性の低いモノマーに比べて高くなっている。
攪拌機および還流冷却器を備えた三っ口500mLフラスコに平均粒径10μmの二酸化珪素50gを充填し、メタノール300mL、蒸留水50mL、酢酸10mLおよびシランカップリング剤である3-(trimethoxysilyl)propyl 2-chloro-2-phenylacetate5g(15.0mmol)を順次添加した。得られたサスペンションを攪拌しながら、オイルバスにて還流が開始される温度まで加熱した。その後、カップリング反応を10時間行った。反応終了後のサスペンションは減圧濾過・イオン交換水洗浄を繰り返し、余分な酢酸等を除去した。その後、凍結乾燥を行い乾燥した。収量は51gであった。FT-IRによる本粉末のスペクトルにはアルカンの吸収が明瞭に認められ、カップリング反応による重合開始剤の導入が行われたことを確認した。なお、重合開始剤の理論導入率は0.3mmol/gである。
ベーキングを行った3方活栓付500mL容積シュレンク重合管に、上述のカップリング粒子の調製によって調製した重合開始剤導入済二酸化珪素粒子100g(重合開始剤濃度30mmol相当)、重合反応追跡用重合開始剤(ethyl 2-chloro-2-phenylacetate;ECPA)30mmol;6.0g、クロロ(インデニル)(ビストリフェニルフォスフィン)ルテニウム(以下Ru(Ind)Cl(PPh3)2とする)0.6mmol;466mg を精秤し、Anisole(重合溶媒)300mL, tetralin(重合反応追跡用内部標準)10mL,n-Bu3N(重合助触媒)6mmol;1.11g,メチルメタアクリレート(MMA)0.6mol;60.0g の順にアルゴン気流下にて注入した。そのシュレンク重合管を所定温度に加温しRu(Ind)Cl(PPh3)2 を完全に溶解させマグネティック攪拌下にて重合反応を開始した。適宜、反応サスペンションをアルゴン気流下にて抜き取り、1H−NMRにてモノマー転化率を測定した。モノマー転化率が90%になった時点でグリシジルメタクリレート(GMA)0.3mol;42.6gを添加し、再度加熱を続けブロックポリマーの重合を行った。この反応サスペンションも適宜、アルゴン気流下にて抜き取り、1H−NMRにてモノマー転化率を測定した。モノマー転化率が90%になった時点で重合反応を終了し、減圧濾過・アセトン洗浄を繰り返した。得られたアセトンを若干含んだスラリーはイオン交換水にて溶媒置換し、凍結乾燥した。
ベーキングを行った3方活栓付500mL容積シュレンク重合管に、上述のカップリング粒子の調製によって調製した重合開始剤導入済二酸化珪素粒子100g(重合開始剤濃度30mmol相当)、重合反応追跡用重合開始剤(ethyl 2-chloro-2-phenylacetate;ECPA)30mmol;6.0g、クロロ(インデニル)(ビストリフェニルフォスフィン)ルテニウム(以下Ru(Ind)Cl(PPh3)2とする)0.6mmol;466mg を精秤し、Anisole(重合溶媒)300mL, tetralin(重合反応追跡用内部標準)10mL、n-Bu3N(重合助触媒)6mmol;1.11g,トリエチレングリコールモノメタアクリレート(TEGMM)0.2mol;53.3gの順にアルゴン気流下にて注入した。そのシュレンク重合管を所定温度に加温しRu(Ind)Cl(PPh3)2 を完全に溶解させマグネティック攪拌下にて重合反応を開始した。適宜、反応サスペンションをアルゴン気流下にて抜き取り、1H−NMRにてモノマー転化率を測定した。モノマー転化率が90%になった時点でグリシジルメタクリレート(GMA)0.3mol;42.6gを添加し、再度加熱を続けブロックポリマーの重合を行った。この反応サスペンションも適宜、アルゴン気流下にて抜き取り、1H−NMRにてモノマー転化率を測定した。モノマー転化率が90%になった時点で重合反応を終了し、減圧濾過・アセトン洗浄を繰り返した。得られたアセトンを若干含んだスラリーはイオン交換水にて溶媒置換し、凍結乾燥した。次に、合成した粉末全量をヒドロキノンモノメチルエーテルを含む脱水アニソール中300mLに分散し、メタクリル酸モノマー0.45mol;38.7gを添加した。その溶液を60℃に加温し3時間反応させた。反応終了後、減圧濾過・アセトン洗浄を繰り返した。得られたアセトンを若干含んだスラリーはイオン交換水にて溶媒置換し、凍結乾燥した。二酸化珪素にグラフトされたポリマーはフッ化水素にて二酸化珪素を溶解した後に、沈殿精製し実施例1同様に1H−NMR、MALDI-TOF-MS、GPCにて同定した。
ベーキングを行った3方活栓付500mL容積シュレンク重合管に粒子調製例1で調製した重合開始剤導入済二酸化珪素粒子100g(重合開始剤濃度30mmol相当)、重合反応追跡用重合開始剤(ethyl 2-chloro-2-phenylacetate;ECPA)30mmol;6.0g、クロロ(インデニル)(ビストリフェニルフォスフィン)ルテニウム(以下Ru(Ind)Cl(PPh3)2とする)0.6mmol;466mg を精秤し、Anisole(重合溶媒)300mL, tetralin(重合反応追跡用内部標準)10mL、n-Bu3N(重合助触媒)6mmol;1.11g,2-ヒドロキシエチルメタアクリレート(2-HEMA)0.4mol;52.1gの順にアルゴン気流下にて注入した。そのシュレンク重合管を所定温度に加温しRu(Ind)Cl(PPh3)2 を完全に溶解させマグネティック攪拌下にて重合反応を開始した。適宜、反応サスペンションをアルゴン気流下にて抜き取り、1H−NMRにてモノマー転化率を測定した。モノマー転化率が90%になった時点でスチレンモノマー0.4mol;41.7gを添加し、再度加熱を続けブロックポリマーの重合を行った。この反応サスペンションも適宜、アルゴン気流下にて抜き取り、1H−NMRにてモノマー転化率を測定した。モノマー転化率が90%になった時点で重合反応を終了した。反応終了後、減圧濾過・アセトン洗浄を繰り返した。得られたアセトンを若干含んだスラリーはイオン交換水にて溶媒置換し、凍結乾燥した。二酸化珪素にグラフトされたポリマーはフッ化水素にて二酸化珪素を溶解した後に、沈殿精製し実施例1同様に1H−NMR、MALDI-TOF-MS、GPCにて同定した。
ベーキングを行った3方活栓付500mL容積シュレンク重合管に上述のカップリング粒子の調製によって調製した重合開始剤導入済二酸化珪素粒子100g(重合開始剤濃度30mmol相当)、重合反応追跡用重合開始剤(ethyl 2-chloro-2-phenylacetate;ECPA)30mmol;6.0g、クロロ(インデニル)(ビストリフェニルフォスフィン)ルテニウム(以下Ru(Ind)Cl(PPh3)2とする)0.6mmol;466mg を精秤し、Anisole(重合溶媒)300mL, tetralin(重合反応追跡用内部標準)10mL、n-Bu3N(重合助触媒)6mmol;1.11g,メチルメタアクリレート(MMA)0.6mol;60.0g,グリシジルアクリレート(GA)0.3mol;38.4gの順にアルゴン気流下にて注入した。そのシュレンク重合管を所定温度に加温しRu(Ind)Cl(PPh3)2 を完全に溶解させマグネティック攪拌下にて重合反応を開始した。適宜、反応サスペンションをアルゴン気流下にて抜き取り、1H−NMRにてモノマー転化率を測定した。モノマー転化率が90%になった時点で重合反応を終了し、減圧濾過・アセトン洗浄を繰り返した。得られたアセトンを若干含んだスラリーはイオン交換水にて溶媒置換し、凍結乾燥した。次に、合成した粉末全量をヒドロキノンモノメチルエーテルを含む脱水アニソール中300mLに分散し、メタクリル酸モノマー0.45mol;38.7gを添加した。その溶液を60℃に加温し3時間反応させた。反応終了後、減圧濾過・アセトン洗浄を繰り返した。得られたアセトンを若干含んだスラリーはイオン交換水にて溶媒置換し、凍結乾燥した。二酸化珪素にグラフトされたポリマーはフッ化水素にて二酸化珪素を溶解した後に、沈殿精製し実施例1同様に1H−NMR、MALDI-TOF-MS、GPCにて同定した。
攪拌機および還流冷却器を備えた三っ口500mLフラスコに平均粒径10μmの二酸化珪素50gを充填し、メタノール300mL、蒸留水50mL、酢酸10mLおよびシランカップリング剤であるKBM-503(信越化学製シランカップリング剤)5gを順次添加した。得られたサスペンションを攪拌しながら、オイルバスにて還流が開始される温度まで加熱した。その後、カップリング反応を10時間行った。反応終了後のサスペンションは減圧濾過・イオン交換水洗浄を繰り返し、余分な酢酸等を除去した。その後、凍結乾燥を行い乾燥した。収量は50gであった。FT-IRによる本粉末のスペクトルにはエチレン性不飽和基の吸収が明瞭に認められ、カップリング反応によるエチレン性不飽和基の導入が行われたことを確認した。このエチレン性不飽和基の理論導入率は0.40mmol/gであった。
次に、上記実施例1〜4の各複合粒子をそれぞれ含む硬化性組成物としての歯科用コンポジットレジンを下記のようにそれぞれ調製し、実施例5〜8とした。
上記比較例1の粒子を含む歯科用コンポジットレジンを下記のように調製し、比較例2とした。
上述したコンポジットレジン調製にて作製したコンポジットレジンの硬化前後の密度変化をAnton Paar製密度測定装置DMAGeneration Mにて測定し、重合後の収縮率を算出した。なお、硬化は約0.5mLの各コンポジットレジンに株式会社松風製LED光照射器ブルーショットにて30秒間光照射し硬化させた。試験結果を表1に示す。なお、重合収縮試験は、各実施例5〜8および比較例2について、それぞれ3回行った。
Claims (7)
- 粒子の表面に、高分子鎖が結合された複合粒子であって、
前記高分子鎖が、少なくとも2種類のモノマーを共重合させたコポリマーを有し、前記少なくとも2種類のモノマーは、当該複合粒子が分散される重合性モノマーに対する親和性が異なるものであり、
前記高分子鎖のモノマー組成は、該高分子鎖の前記粒子の表面に結合している基端部側では、前記重合性モノマーに対する親和性の低いモノマーが前記親和性の高いモノマーに比べて高く、前記高分子鎖の先端部側では、前記親和性の高いモノマーが前記親和性の低いモノマーに比べて高くなっている、
ことを特徴とする複合粒子。 - 前記重合性モノマーがラジカル重合性モノマーであり、
前記高分子鎖の前記先端部側の前記親和性の高いモノマーからなるコポリマーには、重合性基および疎水結合性基の少なくともいずれか一方が結合している、
請求項1に記載の複合粒子。 - 前記ラジカル重合性モノマーが、アクリロイル基、メタアクリロイル基、アリル基を有する化合物である、
請求項2に記載の複合粒子。 - 前記コポリマーが、ブロックコポリマーまたはグラジェントコポリマーである、
請求項1ないし3のいずれかに記載の複合粒子。 - 前記粒子が、二酸化珪素、酸化アルミニウム、および、フルオロアルミノシリケートガラスのうちの少なくとも1種である、
請求項1ないし4のいずれかに記載の複合粒子。 - 前記請求項1ないし5のいずれかに記載の複合粒子および前記重合性モノマーを含む硬化性組成物。
- 当該硬化性組成物が、医科、歯科用に用いられる請求項6に記載の硬化性組成物。
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Cited By (4)
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WO2015029909A1 (ja) * | 2013-08-30 | 2015-03-05 | 横浜ゴム株式会社 | タイヤ用ゴム組成物及びこれを用いる空気入りタイヤ |
EP3042645A1 (de) * | 2015-01-09 | 2016-07-13 | Ivoclar Vivadent AG | Dentalkomposite mit verbesserter Lagerstabilität |
WO2018084121A1 (ja) * | 2016-11-01 | 2018-05-11 | 太陽ホールディングス株式会社 | プリント配線板用の硬化性絶縁性組成物、ドライフィルム、硬化物、プリント配線板およびプリント配線板用の硬化性絶縁性組成物の製造方法 |
US10898415B2 (en) | 2019-01-02 | 2021-01-26 | Kerr Corporation | Fillers for dental restorative materials |
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Cited By (11)
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WO2015029909A1 (ja) * | 2013-08-30 | 2015-03-05 | 横浜ゴム株式会社 | タイヤ用ゴム組成物及びこれを用いる空気入りタイヤ |
JP6077123B2 (ja) * | 2013-08-30 | 2017-02-08 | 横浜ゴム株式会社 | タイヤ用ゴム組成物及びこれを用いる空気入りタイヤ |
US9598563B2 (en) | 2013-08-30 | 2017-03-21 | The Yokohama Rubber Co., Ltd. | Rubber composition for tires, and pneumatic tire manufactured using same |
EP3042645A1 (de) * | 2015-01-09 | 2016-07-13 | Ivoclar Vivadent AG | Dentalkomposite mit verbesserter Lagerstabilität |
WO2016110571A1 (de) * | 2015-01-09 | 2016-07-14 | Ivoclar Vivadent Ag | Dentalkomposite mit verbesserter lagerstabilität |
EP3042645B1 (de) | 2015-01-09 | 2022-04-27 | Ivoclar Vivadent AG | Dentalkomposite mit verbesserter Lagerstabilität |
US11357708B2 (en) | 2015-01-09 | 2022-06-14 | Ivoclar Vivadent Ag | Dental composites with improved storage stability |
WO2018084121A1 (ja) * | 2016-11-01 | 2018-05-11 | 太陽ホールディングス株式会社 | プリント配線板用の硬化性絶縁性組成物、ドライフィルム、硬化物、プリント配線板およびプリント配線板用の硬化性絶縁性組成物の製造方法 |
CN109892021A (zh) * | 2016-11-01 | 2019-06-14 | 太阳控股株式会社 | 印刷电路板用固化性绝缘性组合物、干膜、固化物、印刷电路板及印刷电路板用固化性绝缘性组合物的制造方法 |
JPWO2018084121A1 (ja) * | 2016-11-01 | 2019-09-19 | 太陽ホールディングス株式会社 | プリント配線板用の硬化性絶縁性組成物、ドライフィルム、硬化物、プリント配線板およびプリント配線板用の硬化性絶縁性組成物の製造方法 |
US10898415B2 (en) | 2019-01-02 | 2021-01-26 | Kerr Corporation | Fillers for dental restorative materials |
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