JP2014504303A - 硬化性組成物 - Google Patents
硬化性組成物 Download PDFInfo
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- JP2014504303A JP2014504303A JP2013513449A JP2013513449A JP2014504303A JP 2014504303 A JP2014504303 A JP 2014504303A JP 2013513449 A JP2013513449 A JP 2013513449A JP 2013513449 A JP2013513449 A JP 2013513449A JP 2014504303 A JP2014504303 A JP 2014504303A
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- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- UZIAQVMNAXPCJQ-UHFFFAOYSA-N triethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)COC(=O)C(C)=C UZIAQVMNAXPCJQ-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 150000003755 zirconium compounds Chemical class 0.000 description 1
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Abstract
【解決手段】一分子に平均して1個未満の加水分解性ケイ素基を有し、オキシエチレン単位の含有量が5〜80重量%である有機重合体(I)を含有する硬化性組成物。
【選択図】なし
Description
(1)一分子に平均して1個未満の加水分解性ケイ素基を有し、オキシエチレン単位の含有量が5〜80重量%である有機重合体(I)を含有する硬化性組成物、
(2)有機重合体(I)が、オキシエチレン単位を5〜80重量%含有するポリオキシアルキレン系重合体であることを特徴とする(1)記載の硬化性組成物、
(3)有機重合体(I)が1個の活性水素を有する化合物を出発原料として製造されることを特徴とする(1)または(2)記載の硬化性組成物、
(4)有機重合体(I)が出発原料の活性水素を加水分解性ケイ素基に変換して製造されることを特徴とする(1)〜(3)のいずれか1項に記載の硬化性組成物、
(5)有機重合体(I)の数平均分子量が500〜15,000であることを特徴とする(1)〜(4)のいずれか1項に記載の硬化性組成物、
(6)有機重合体(I)がエチレンオキサイドとプロピレンオキサイドとの共重合体であることを特徴とする(1)〜(5)のいずれか1項に記載の硬化性組成物、
(7)1分子に平均して1個以上の加水分解性ケイ素基を有する有機重合体(II)100重量部、(1)〜(6)のいずれか1項に記載の有機重合体(I)5〜200重量部を含むことを特徴とする硬化性組成物、
(8)有機重合体(II)が、ポリオキシアルキレン系重合体であることを特徴とする(7)記載の硬化性組成物、
(9)有機重合体(II)の主鎖がオキシプロピレン単位からなることを特徴とする(7)または(8)記載の硬化性組成物、
(10)有機重合体(II)の数平均分子量が2,000〜50,000であることを特徴とする(7)〜(9)のいずれか1項に記載の硬化性組成物、
(11)有機重合体(II)が複合金属シアン化物錯体触媒を用いたアルキレンオキシドの開環付加重合で製造されることを特徴とする(7)〜(10)のいずれか1項に記載の硬化性組成物、
(12)有機重合体(II)の主鎖骨格中に、一般式(2):
−NR5−C(=O)− (2)
(R5は水素原子または1価の有機基である)で表される基を有することを特徴とする(7)〜(11)のいずれか1項に記載の硬化性組成物、
(13)有機重合体(II)100重量部、有機重合体(I)5〜200重量部、充填材1〜250重量部、アミノ基含有シランカップリング剤0.1〜20重量部、硬化触媒0.01〜10重量部、を含むことを特徴とする(7)〜(12)のいずれか1項に記載の硬化性組成物、
(14)(1)〜(13)のいずれか1項に記載の硬化性組成物からなる塗膜防水材、
に関する。
反応性ケイ素基を有する有機重合体(I)、及び/または(II)中に含有される反応性ケイ素基は、ケイ素原子に結合した水酸基又は加水分解性基を有し硬化触媒によって触媒される反応によりシロキサン結合を形成することにより架橋しうる基である。代表例としては、
H−(SiR3 2O)mSiR3 2−R4−SiX3 (1)
(式中、Xは前記に同じ。2×m+2個のR3は、それぞれ独立に、炭化水素基または−OSi(R’’)3(R’’は、それぞれ独立に、炭素原子数1から20の置換あるいは非置換の炭化水素基である)で示されるトリオルガノシロキシ基であり、入手性およびコストの点から、炭素原子数1から20の炭化水素基が好ましく、炭素原子数1から8の炭化水素基がより好ましく、炭素原子数1から4の炭化水素基が特に好ましい。R4は2価の有機基であり、入手性およびコストの点から、炭素原子数1から12の2価の炭化水素基が好ましく、炭素原子数2から8の2価の炭化水素基がより好ましく、炭素原子数2の2価の炭化水素基が特に好ましい。また、mは、0から19の整数であり、入手性およびコストの点から、1が好ましい)で表されるシラン化合物は、不均化反応が進まない。このため、(イ)の合成法で、3個の加水分解性基が1つのケイ素原子に結合している基を導入する場合には、一般式(1)で表されるシラン化合物を用いることが好ましい。一般式(1)で示されるシラン化合物の具体例としては、1−[2−(トリメトキシシリル)エチル]−1,1,3,3−テトラメチルジシロキサン、1−[2−(トリメトキシシリル)プロピル]−1,1,3,3−テトラメチルジシロキサン、1−[2−(トリメトキシシリル)ヘキシル]−1,1,3,3−テトラメチルジシロキサンが挙げられる。
−NR5−C(=O)− (2)
(R5は水素原子または1価の有機基であり、好ましくは炭素原子数1から20の置換あるいは非置換の1価の炭化水素基であり、より好ましくは炭素原子数1から8の置換あるいは非置換の1価の炭化水素基である)で表される基である。
−CH2−C(R6)(COOR7)− (3)
(式中、R6は水素原子またはメチル基、R7は炭素原子数1から8のアルキル基を示す)で表される炭素原子数1から8のアルキル基を有する(メタ)アクリル酸エステル単量体単位と、下記一般式(4):
−CH2−C(R6)(COOR8)− (4)
(式中、R6は前記に同じ、R8は炭素原子数10以上のアルキル基を示す)で表される炭素原子数10以上のアルキル基を有する(メタ)アクリル酸エステル単量体単位からなる共重合体に、反応性ケイ素基を有するポリオキシアルキレン系重合体をブレンドして製造する方法である。
R9−OH (5)
(式中、R9は不飽和基を有しない炭素、水素、酸素及び窒素からなる群より選択される1種以上を構成原子として含有する1価の有機基である。)
で表される化合物が挙げられる。
反応性ケイ素基を有する有機重合体(II)の一例である反応性ケイ素基を有するポリオキシアルキレン系重合体は比較的低粘度である為、本発明の硬化性組成物は塗布可能な粘度に設計し易い。更に、本発明の硬化性組成物を硬化して得られる硬化物は、透湿性が高く、かつ、外部からの水の侵入を防ぐ為の十分な防水性を有する。従って、本発明の硬化性組成物は、建物用の防水材として有用で、特に、透湿性塗膜防水材として有用である。透湿性塗膜防水材とは、硬化前は液状で、ハケやヘラ、ローラーなどで下地に塗布するか、あるいは吹付機により施工して成膜・硬化させ、シームレスな防水層を形成する防水材であって、透湿性を有するために、下地からの水分を外部に放出することが可能な塗膜防水材である。塗膜防水材は、(i)シームレスな塗膜を形成するので、継ぎ目がなく防水の信頼性が高い、(ii)複雑な形状の部位にも対応できる、等の特長がある。
ブタノールを開始剤とし、アルカリ金属触媒(KOH)を用いて重合した分子量2,400のエチレンオキシド/プロピレンオキシドブロック共重合体=50/50(モル比)のブトキシ片末端のポリオキシアルキレンモノオールの水酸基に対して、1.2倍等量のNaOCH3のメタノール溶液を添加してメタノールを留去し、さらに塩化アリルを添加して末端の水酸基をアリルオキシ基に変換した。脱塩精製処理を実施して得られた片末端アリルオキシポリオキシプロピレン重合体600gに対して、共沸溶剤としてヘキサンを加えて90℃で共沸脱水を行い、ヘキサンを減圧下留去した後、窒素置換した。これに対して、白金ビニルシロキサン錯体の白金含量3重量%のイソプロパノール溶液を120μl加え、攪拌しながら、ジメトキシメチルシラン27gを90℃で6時間反応させた後、減圧脱気することにより、分子量が2,400のジメトキシメチルシリル基を有するブトキシ片末端のポリオキシアルキレン重合体(A−1)を得た。1H−NMR(日本電子製JNM−LA400を用いて、CDCl3溶媒中で測定)の測定の結果、ジメトキシメチルシリル基は1分子あたり平均して0.8個であった。
メタノールを開始剤とし、アルカリ金属触媒(KOH)を用いて重合した分子量約1,500のエチレンオキシド/プロピレンオキシドブロック共重合体=47/53(モル比)のメトキシ片末端のポリオキシアルキレンモノオールの水酸基に対して、1.2倍等量のNaOCH3のメタノール溶液を添加してメタノールを留去し、さらに塩化アリルを添加して末端の水酸基をアリルオキシ基に変換した。脱塩精製処理を実施して得られた片末端アリルオキシポリオキシプロピレン重合体600gに対して、共沸溶剤としてヘキサンを加えて90℃で共沸脱水を行い、ヘキサンを減圧下留去した後、窒素置換した。これに対して、白金ビニルシロキサン錯体の白金含量3重量%のイソプロパノール溶液を120μl加え、攪拌しながら、ジメトキシメチルシラン49.8gを90℃で6時間反応させた後、減圧脱気することにより、分子量が約1,500のジメトキシメチルシリル基を有するメトキシ片末端のポリオキシアルキレン重合体(A−2)を得た。1H−NMR(日本電子製JNM−LA400を用いて、CDCl3溶媒中で測定)の測定の結果、ジメトキシメチルシリル基は1分子あたり平均して0.8個であった。
ポリプロピレングリコールを開始剤とし、亜鉛ヘキサシアノコバルテートグライム錯体触媒にてテトラヒドロフラン存在下、プロピレンオキシドの重合を行い、分子量約10,000の水酸基末端ポリオキシプロピレン重合体を得た。続いて、この水酸基末端ポリオキシプロピレン重合体の水酸基に対して1.2倍当量のNaOCH3のメタノール溶液を添加してメタノールを留去し、さらに塩化アリルを添加して末端の水酸基をアリルオキシ基に変換した。脱塩精製処理を実施して得られたアリルオキシ末端ポリオキシプロピレン重合体2,000gに対し、酸化防止剤として2,6ジ−tert−ブチル−p−クレゾール、共沸溶剤としてヘキサンを加えて90℃で共沸脱水を行い、ヘキサンを減圧下留去した後、窒素置換した。これに対して、白金ビニルシロキサン錯体の白金含量3重量%のイソプロパノール溶液を100μl加え、攪拌しながら、ジメトキシメチルシラン35.4gを90℃で2時間反応させた後、減圧脱気することにより、分子量が約10,000のジメトキシメチルシリル基を有する直鎖構造のポリオキシプロピレン重合体(B−1)を得た。1H−NMR(日本電子製JNM−LA400を用いて、CDCl3溶媒中で測定)の測定の結果、ジメトキシメチルシリル基は1分子あたり平均して1.6個であった。
ポリプロピレントリオールを開始剤とし、亜鉛ヘキサシアノコバルテートグライム錯体触媒にてテトラヒドロフラン存在下、プロピレンオキシドの重合を行い、分子量約12,000の分岐構造の水酸基末端ポリオキシプロピレン重合体を得た。続いて、この水酸基末端ポリオキシプロピレン重合体の水酸基に対して1.2倍当量のNaOCH3のメタノール溶液を添加してメタノールを留去し、さらに塩化アリルを添加して末端の水酸基をアリルオキシ基に変換した。脱塩精製処理を実施して得られたアリルオキシ末端ポリオキシプロピレン重合体2,000gに対し、酸化防止剤として2,6ジ−tert−ブチル−p−クレゾール、共沸溶剤としてヘキサンを加えて90℃で共沸脱水を行い、ヘキサンを減圧下留去した後、窒素置換した。これに対して、白金ビニルシロキサン錯体の白金含量3重量%のイソプロパノール溶液を100μl加え、攪拌しながら、ジメトキシメチルシラン35.6gを90℃で2時間反応させた後、減圧脱気することにより、分子量が約12,000のジメトキシメチルシリル基を有する分岐構造のポリオキシプロピレン重合体(B−2)を得た。1H−NMR(日本電子製JNM−LA400を用いて、CDCl3溶媒中で測定)の測定の結果、ジメトキシメチルシリル基は1分子あたり平均して2.2個であった。
水酸基当量が0.36mmol/gであり、分子量が約5,000のポリオキシプロピレンジオール100g(20mmol)と、NCO/OHの比が1.25となるMDI(4,4’−ジフェニルメタンジイソシアネート、和光純薬工業製)5.6g(22.5mmol)を窒素雰囲気下で混合し、90℃で3時間反応させ、NCO末端ポリオキシプロピレンを得た後、γ−アミノプロピルトリメトキシシラン(モメンティブ・パフォーマンス・マテリアルズ製)1.6g(9mmol)を追加し、40℃で1時間反応させた後、減圧脱気することにより、トリメトキシシリル基末端ポリオキシプロピレン(B−3)を得た。また、1H−NMRを用い、シリル基導入率を調べた結果、末端のトリメトキシシリル基は1分子あたり平均して1.7個であった。
分子量約3,000のポリオキシプロピレングリコールを開始剤とし、亜鉛ヘキサシアノコバルテートグライム錯体触媒にてテトラヒドロフラン存在下、プロピレンオキシドの重合を行い、末端が水酸基である分子量約17,000の2官能ポリプロピレンオキシド(これを重合体Qとする)を得た。
ブタノールを開始剤とし、亜鉛ヘキサシアノコバルテートグライム錯体触媒にてテトラヒドロフラン存在下、プロピレンオキシドを用いた重合を行い、分子量約5,400の水酸基末端ポリオキシプロピレン重合体を得た。続いて、この水酸基末端ポリオキシプロピレン重合体の水酸基に対して1.2倍当量のNaOCH3のメタノール溶液を添加してメタノールを留去し、さらに塩化アリルを添加して末端の水酸基をアリルオキシ基に変換した。脱塩精製処理を実施して得られたアリルオキシ末端ポリオキシプロピレン重合体2,000gに対し、酸化防止剤として2,6ジ−tert−ブチル−p−クレゾール、共沸溶剤としてヘキサンを加えて90℃で共沸脱水を行い、ヘキサンを減圧下留去した後、窒素置換した。これに対して、白金ビニルシロキサン錯体の白金含量3重量%のイソプロパノール溶液を100μl加え、攪拌しながら、ジメトキシメチルシラン37.2gを90℃で2時間反応させた後、減圧脱気することにより、分子量が約5,400のジメトキシメチルシリル基を有するポリオキシプロピレン重合体(C−1)を得た。1H−NMR(日本電子製JNM−LA400を用いて、CDCl3溶媒中で測定)の測定の結果、ジメトキシメチルシリル基は1分子あたり平均して0.96個であった。
表1に示す処方にしたがって、有機重合体(I)、有機重合体(II)、可塑剤、充填剤、チクソ性付与剤、各種安定剤、脱水剤、接着付与剤および硬化触媒などをそれぞれ計量し、ミキサーを用いて、脱水条件下にて実質的に水分の存在しない状態で混練した後、防湿性の容器(ポリエチレン製カートリッジ)に密閉し、1液型硬化性組成物を得た。表1の1液型組成物は、使用時に各カートリッジから各1液型組成物を押し出し、後述の評価を行った。
<可塑剤>Ucon LB−65(ダウケミカル製、ポリプロピレングリコール)
Ucon 50−HB−260(ダウケミカル製、ポリプロピレングリコール−ポリエチレングリコールブロックポリマー)
<膠質炭酸カルシウム>Ultra−Pflex(スペシャルティミネラルズ製)
<表面処理重質炭酸カルシウム>Hubercarb G2T(Huber Engineered Materials製)
<酸化チタン>Ti−Pure R902+(デュポン製)
<チクソ性付与剤>Crayvallac SL(クレー・バレー製、アマイドワックス系チクソ性付与剤)
<紫外線吸収剤>チヌビン328(チバ・スペシャルティ・ケミカルズ製)
<光安定剤>チヌビン770(チバ・スペシャルティ・ケミカルズ製)
<アミノ基含有シランカップリング剤>A−1120(モメンティブ・パフォーマンス・マテリアルズ製、N−(β−アミノエチル)−γ−アミノプロピルトリメトキシシラン)
<その他シランカップリング剤>A-171(モメンティブ・パフォーマンス・マテリアルズ製、ビニルトリメトキシシラン)
<硬化触媒>ネオスタンU-220H(日東化成製、ジブチルスズビスアセチルアセトナート)
FomrezSUL−4(モメンティブ・パフォーマンス・マテリアルズ製、ジブチルスズジラウレート)
ASTM E96のWater Method(ウェットカップ法)に準じて評価した。
表1の各組成物を、テフロン(登録商標)フィルム上に塗布し、厚さ約30milとなるようにスペーサーと平スパチュラで調整した後、恒温恒湿室(23℃/50%RH)で4日間、そして50℃オーブン中で3日間、養生した。養生後、硬化物シートをカップサイズに切り取り、厚み(α)を測定した。Gardco社製,透湿度測定専用カップへ水を約15g入れた後、硬化物シート、クランピングリング、キャップの順にセットした。重量を測定した後、恒温恒湿室(23℃/50%RH)で4日間に亘り、約24時間間隔で重量を測定し、透湿度(β)を算出した。更に、(α)、(β)値を使用し、透湿性[α×β/1000」(単位:Perm・inch)を算出した。
表1の各組成物を、テフロン(登録商標)フィルム上に塗布し、厚さ約30milとなるようにスペーサーと平スパチュラで調整した後、恒温恒湿室(23℃/50%RH)で4日間、そして50℃オーブン中で3日間、養生し、塗膜状の硬化物を得た。恒温恒湿室(23℃/50%RH)又は15℃/95%RH下で放置し、塗膜表面への可塑剤の移行を目視と指触で評価した。可塑剤の移行が認められない場合Aとし、可塑剤の移行が僅かに認められた場合Bとし、可塑剤の移行が明らかに認められた場合Cとし、著しく可塑剤の移行が認められた場合Dとした。
表1の各組成物を、テフロン(登録商標)フィルム上に塗布し、厚さ約3cmとなるようにスペーサーと平スパチュラで調整した後、恒温恒湿室(23℃/50%RH)で4日間、そして50℃オーブン中で3日間養生し、その後硬化物を約1inchx1inchサイズに切り取った。各サンプルの重量(W1)を測定した後、純水の入ったガラス瓶の中へ入れ、恒温恒湿室で1週間静置した。サンプルを水中から取り出した後、70℃オーブン中で1週間水分を蒸発させた。恒温恒湿室で数時間静置した後、重量(W2)を測定し、各サンプルの可塑剤の流出率(R)を算出した。
R=(W2−W1)/W1×100(%)
Claims (14)
- 一分子に平均して1個未満の加水分解性ケイ素基を有し、オキシエチレン単位の含有量が5〜80重量%である有機重合体(I)を含有する硬化性組成物。
- 有機重合体(I)が、オキシエチレン単位を5〜80重量%含有するポリオキシアルキレン系重合体であることを特徴とする請求項1記載の硬化性組成物。
- 有機重合体(I)が1個の活性水素を有する化合物を出発原料として製造されることを特徴とする請求項1または2記載の硬化性組成物。
- 有機重合体(I)が出発原料の活性水素を加水分解性ケイ素基に変換して製造されることを特徴とする請求項1〜3のいずれか1項に記載の硬化性組成物。
- 有機重合体(I)の数平均分子量が500〜15,000であることを特徴とする請求項1〜4のいずれか1項に記載の硬化性組成物。
- 有機重合体(I)がエチレンオキサイドとプロピレンオキサイドとの共重合体であることを特徴とする請求項1〜5のいずれか1項に記載の硬化性組成物。
- 1分子に平均して1個以上の加水分解性ケイ素基を有する有機重合体(II)100重量部、請求項1〜6のいずれか1項に記載の有機重合体(I)5〜200重量部を含むことを特徴とする硬化性組成物。
- 有機重合体(II)が、ポリオキシアルキレン系重合体であることを特徴とする請求項7記載の硬化性組成物。
- 有機重合体(II)の主鎖がオキシプロピレン単位からなることを特徴とする請求項7または8記載の硬化性組成物。
- 有機重合体(II)の数平均分子量が2,000〜50,000であることを特徴とする請求項7〜9のいずれか1項に記載の硬化性組成物。
- 有機重合体(II)が複合金属シアン化物錯体触媒を用いたアルキレンオキシドの開環付加重合で製造されることを特徴とする請求項7〜10のいずれか1項に記載の硬化性組成物。
- 有機重合体(II)の主鎖骨格中に、一般式(2):
−NR5−C(=O)− (2)
(R5は水素原子または1価の有機基である)で表される基を有することを特徴とする請求項7〜11のいずれか1項に記載の硬化性組成物。 - 有機重合体(II)100重量部、有機重合体(I)5〜200重量部、充填材1〜250重量部、アミノ基含有シランカップリング剤0.1〜20重量部、硬化触媒0.01〜10重量部、を含むことを特徴とする請求項7〜12のいずれか1項に記載の硬化性組成物。
- 請求項1〜13のいずれか1項に記載の硬化性組成物からなる塗膜防水材。
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WO2023210470A1 (ja) * | 2022-04-26 | 2023-11-02 | Agc株式会社 | 化合物、組成物、表面処理剤、物品の製造方法、及び物品 |
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US9777189B2 (en) | 2014-11-03 | 2017-10-03 | Kaneka North America Llc | Curable composition |
JP6630367B2 (ja) * | 2015-12-22 | 2020-01-15 | 株式会社カネカ | 複合体の製造方法および複合体 |
CN114127156A (zh) | 2019-02-28 | 2022-03-01 | 钟化美洲控股公司 | 可湿固化粘合剂组合物 |
CN114213648B (zh) * | 2021-12-27 | 2023-06-20 | 安徽壹石通材料科学研究院有限公司 | 一种可水解聚合物以及包含该聚合物的环氧树脂导热材料组合物 |
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