JP6464803B2 - 活性エネルギー線重合性接着剤組成物、及びそれを用いてなる積層体 - Google Patents
活性エネルギー線重合性接着剤組成物、及びそれを用いてなる積層体 Download PDFInfo
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- JP6464803B2 JP6464803B2 JP2015031362A JP2015031362A JP6464803B2 JP 6464803 B2 JP6464803 B2 JP 6464803B2 JP 2015031362 A JP2015031362 A JP 2015031362A JP 2015031362 A JP2015031362 A JP 2015031362A JP 6464803 B2 JP6464803 B2 JP 6464803B2
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- meth
- vinyl
- acid
- ether
- acrylate
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- 230000001070 adhesive effect Effects 0.000 title claims description 58
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- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 38
- 229920000642 polymer Polymers 0.000 claims description 34
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 19
- 125000003277 amino group Chemical group 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
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- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 19
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
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- 239000000126 substance Substances 0.000 description 13
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- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 12
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- 239000003505 polymerization initiator Substances 0.000 description 11
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 9
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- 239000003999 initiator Substances 0.000 description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 description 9
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 8
- 125000002723 alicyclic group Chemical group 0.000 description 8
- 125000001931 aliphatic group Chemical group 0.000 description 8
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- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 6
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- RISDDVKHYROMNH-UHFFFAOYSA-N prop-1-en-2-yloxybenzene Chemical compound CC(=C)OC1=CC=CC=C1 RISDDVKHYROMNH-UHFFFAOYSA-N 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
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- 239000004743 Polypropylene Substances 0.000 description 5
- XQBCVRSTVUHIGH-UHFFFAOYSA-L [dodecanoyloxy(dioctyl)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCC XQBCVRSTVUHIGH-UHFFFAOYSA-L 0.000 description 5
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
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- YJGJRYWNNHUESM-UHFFFAOYSA-J triacetyloxystannyl acetate Chemical compound [Sn+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O YJGJRYWNNHUESM-UHFFFAOYSA-J 0.000 description 1
- CDMIYIVDILNBIJ-UHFFFAOYSA-N triazinane-4,5,6-trithione Chemical compound SC1=NN=NC(S)=C1S CDMIYIVDILNBIJ-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- BDIWFCKBPZPBQT-UHFFFAOYSA-N tributyl(tributylstannylsulfanyl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)S[Sn](CCCC)(CCCC)CCCC BDIWFCKBPZPBQT-UHFFFAOYSA-N 0.000 description 1
- NXFZDTAAMQLJEC-UHFFFAOYSA-M tributyl-(2,2,2-trichloroacetyl)oxytin(1-) Chemical compound CCCC[Sn-](CCCC)(CCCC)OC(=O)C(Cl)(Cl)Cl NXFZDTAAMQLJEC-UHFFFAOYSA-M 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- UMFJXASDGBJDEB-UHFFFAOYSA-N triethoxy(prop-2-enyl)silane Chemical compound CCO[Si](CC=C)(OCC)OCC UMFJXASDGBJDEB-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- LFRDHGNFBLIJIY-UHFFFAOYSA-N trimethoxy(prop-2-enyl)silane Chemical compound CO[Si](OC)(OC)CC=C LFRDHGNFBLIJIY-UHFFFAOYSA-N 0.000 description 1
- NELVVTIEGZVCKM-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;sulfate Chemical compound [O-]S([O-])(=O)=O.C[N+](C)(C)CCCNC(=O)C=C.C[N+](C)(C)CCCNC(=O)C=C NELVVTIEGZVCKM-UHFFFAOYSA-N 0.000 description 1
- VUWVDNLZJXLQPT-UHFFFAOYSA-N tripropoxy(propyl)silane Chemical compound CCCO[Si](CCC)(OCCC)OCCC VUWVDNLZJXLQPT-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000007740 vapor deposition 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
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- CIBGZAYGXFGOFK-UHFFFAOYSA-L zinc;2-phenylethenesulfonate Chemical compound [Zn+2].[O-]S(=O)(=O)C=CC1=CC=CC=C1.[O-]S(=O)(=O)C=CC1=CC=CC=C1 CIBGZAYGXFGOFK-UHFFFAOYSA-L 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Laminated Bodies (AREA)
- Adhesive Tapes (AREA)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
Description
感圧式接着剤は含有する溶媒成分で分類すると、有機溶剤を使用する溶剤型。水を使用する水溶解型および水分散型。溶剤を使用しない無溶剤型が存在するが、中でも近年は環境調和、省エネルギーの観点から溶媒乾燥が不要で、有機溶剤を使用しない無溶剤型の活性エネルギー線硬化型の感圧式接着剤が注目されている。
無溶剤型の活性エネルギー線硬化型の感圧式接着剤では、溶剤型などと比較して低粘度な低分子量化合物を使用するため、その硬化塗膜は硬いが、柔軟性がなく脆くなりやすい。このためアクリルポリマーに特定のアクリル系のモノマーを添加することで強度と接着性に優れ、かつ、硬化した後の柔軟性が高い感圧式接着剤組成物が示されている(特許文献1)。また、アクリル系ではなくウレタンポリマーを用いて、その末端にラジカル重合開始剤基を付与することで分岐構造を少なくし、強靭で柔軟な塗膜が得られることが示されている(特許文献2)。しかし、これらの接着剤塗膜は依然、強度と柔軟性が十分でないという課題がある。
次にウレタンポリマー(A)について説明する。本発明のウレタンポリマー(A)は末端にチオール基を有するウレタンポリマーである。上述のように末端にチオール基を有することで組成物の硬化膜に強度と柔軟性が付与される。ウレタンポリマー(A)は、ジオールとジイソシアネートのみから反応した場合は、末端は2つであるが、3官能以上のポリオールもしくはポリイソシアネートを含む場合など、鎖の分岐の数に応じて、ウレタンポリマー(A)の有する末端の数は増大する。チオール基はこれら末端の全てもしくは一部に付加していればよく、ウレタンポリマー(A)末端の数の0.1%〜100%であることが好ましい。より好ましくは10%〜90%である。末端すべてがチオール基の場合は硬化後に強固な塗膜となる。チオール基が末端の0.1%未満であると十分に反応できず塗膜の強度が不足する場合がある。
ウレタンポリマー(A)得るための方法は特に制限されることはないが、例えば以下の方法で合成することが出来る。
1)末端にイソシアネート基を有するウレタンプレポリマー(C)に対して、チオール基以外の1つ以上のイソシアネート基と反応する反応性基を有し、且つ1つ以上のチオール基を有する化合物(c−1)を付加させる。
2)末端にイソシアネート基を有するウレタンプレポリマー(C)に対して、2つ以上のチオール基を含有する化合物(c−2)を付加させる。ただし(c−2)は(c−1)の化合物を含まないものとする。
なお、化合物(c−1)もしくは化合物(c−2)は、イソシアネート基と反応する反応性基を2つ以上有しているので、化合物(c−1)もしくは化合物(c−2)の一部は、ウレタンポリマー(A)の内部に取り込まれる。しかし、イソシアネート基と反応する反応性基が1つしか反応しなかった場合、そこが末端となり、末端の少なくとも1つにチオール基を有するウレタンポリマー(A)となる。末端にイソシアネート基を有するウレタンプレポリマー(C)が、化合物(c−1)もしくは化合物(c−2)よりある程度過剰にあったとしても、末端の少なくとも1つにチオール基を有するウレタンポリマー(A)が合成される。
1つ以上のチオール基以外のイソシアネート基と反応する反応性基を有し、且つ1つ以上のチオール基を有する化合物(c−1)としては、例えば、
(分子内に1つの水酸基と1つのチオール基とを有する化合物)
分子内に1つの水酸基と1つのチオール基とを有する化合物として、例えば、メルカプトメタノール、2−メルカプトエタノール、3−メルカプト−1−プロパノール、1−メルカプト−2−ブタノール、2−メルカプト−3−ブタノールなどが挙げられる。
1,2−ジメルカプト−3−プロパノール、1,3−ジメルカプト−2−プロパノール、2,3−ジメルカプト−1−ブタノール、2,4−ジメルカプト−1−ブタノール、3,4−ジメルカプト−1−ブタノール、1,3−ジメルカプト−2−ブタノール、1,4−ジメルカプト−2−ブタノール、3,4−ジメルカプト−2−ブタノール、トリメチロールプロパンジメルカプトアセテートなどが挙げられる。
トリメルカプトペンタエリスリトール《3−メルカプト−2,2−ビス(メルカプトメチル)プロパン−1−オール;CAS:500283−12−5》、ペンタエリトリトールトリス(3−メルカプトアセタート)、ジペンタエリトリトールペンタキス(3−メルカプトプロピオナート)などが挙げられる。
1−メルカプト−1,1−メタンジオール、1−メルカプト−1,1−エタンジオール、3−メルカプト−1,2−プロパンジオール《チオグリセリン》、2−メルカプト−1,2−プロパンジオール、2−メルカプト−2−メチル−1,3−プロパンジオール、2−メルカプト−2−エチル−1,3−プロパンジオール、1−メルカプト−2,2−プロパンジオール、2−メルカプトエチル−2−メチル−1,3−プロパンジオール、2−メルカプトエチル−2−エチル−1,3−プロパンジオールなどが挙げられる。
1,2−ジメルカプト−1,2−エタンジオール、ジメルカプトペンタエリスリトール《1,3−プロパンジオール,2,2−ビス(メルカプトメチル);CAS:19333−66−5》、1,4−ジメルカプトブタン−2,3−ジオール、2,3−ジメルカプト−1,4−ブタンジオール、3,4−ジメルカプトブタン−1,2−ジオール、3−(2,3−ジメルカプトプロポキシ)プロパン−1,2−ジオール、2−(2,3−ジメルカプトプロポキシ)プロパン−1,3−ジオール、ジメルカプトジトリメチロールエタン、ジメルカプトジトリメチロールプロパン《2−((3−ヒドロキシ−2−メルカプトメチル−2−(メチル)プロポキシ)メチル)−3−メルカプト−2−(メチル)プロパン−1−オール》、1,2−ジメルカプトシクロブタジエン−3,4−ジオール、4,5−ジメルカプト−1,2−ベンゼンジオール、2,3−ジメルカプトヒドロキノン、4,6−ジメルカプトレソルシノール、3,6−ジメルカプトベンゼン−1,2−ジメタノール、2,3−ジメルカプトベンゼン−1,4−ジメタノールなどが挙げられる。
トリメルカプトジペンタエリスリトール《2−((3−ヒドロキシ−2,2−ビス(メルカプトメチル)プロポキシ)メチル−2−(メルカプトメチル)プロパン−1,3−ジオール)》、テトラメルカプトジペンタエリスリトール《2−((3−ヒドロキシ−2,2−ビス(メルカプトメチル)プロポキシ)メチル)−3−メルカプト−2−(メルカプトメチル)プロパン−1−オール》などのポリメルカプトポリオールや、ジペンタエリスリトールのトリメルカプトアセテート、テトラメルカプトアセテートなどが挙げられる。
メルカプト酢酸、メルカプトプロピオン酸、メルカプトこはく酸、2−メルカプトニコチン酸、メルカプト安息香酸、11−メルカプトウンデカン酸などが挙げられる。
2−メルカプトイミダゾール、2−メルカプト−1メチルイミダゾール、1−アミノチオール、2−アミノエタンチオール、アミノプロパンチオール、アミノブタンチオール、アミノペンタンチオール、アミノヘキサンチオール、アミノベンゼンチオール、1−アミノ−2−メチル−2−プロパンチオール、1,2−ジメチル−2−アミノエタンチオールなどが挙げられる。
少なくとも2つ以上のチオール基を含有する化合物(c−2)としては例えば、
メタンジチオール、1,3−ブタンジチオール、1,4−ブタンジチオール、2,3−ブタンジチオール、1,2−ベンゼンジチオール、1,3−ベンゼンジチオール、1,4− ベンゼンジチオール、1,10−デカンジチオール、1,2−エタンジチオール、1,6−ヘキサンジチオール、1,9−ノナンジチオール、1,8−オクタンジチオール、1,5− ペンタンジチオール、1,2−プロパンジチオール、1,3−プロパジチオール、トルエン−3,4−ジチオール、3,6−ジクロロ−1,2−ベンゼンジチオール、1,5−ナフタレンジチオール、エチレングリコールビス(2−メルカプトアセテート)、エチレングリコールビス(3−メルカプトプロピオネート)、ジエチレングリコールビス(2−メルカプトアセテート)、ジエチレングリコールビス(3−メルカプトプロピオネート 、1,4−ブタンジオールビス(2−メルカプトアセテート)、1,4−ブタンジオールビス(3−メルカプトプロピオネート)、トリメチロールプロパントリス(2−メルカプトアセテート)、トリメチロールプロパントリス(3−メルカプトプロピオネート)、ペンタエリスリトールテトラキス(2−メルカプトアセテート)、ペンタエリスリトールテトラキス(3−メルカプトプロピオネート 、1,2−ジメルカプトシクロヘキサン、1,3−ジメルカプトシクロヘキサン、1,4−ジメルカプトシクロヘキサン、1,3−ビス(メルカプトメチル)シクロヘキサン、1,4−ビス(メルカプトメチル)シクロヘキサン、2,5−ビス(メルカプトメチル)−1,4−ジチアン、2,5−ビス(2−メルカプトエチル)−1,4−ジチアン、2,5−ビス(2−メルカプトエチルチオメチル)−1,4−ジチアン、2,5−ビス(メルカプトメチル)−1−チアン、2,5−ビス(2−メルカプトエチル)−1−チアン、2,5−ビス(メルカプトメチル)チオフェン、1,2 −ジメルカプトベンゼン、1,3−ジメルカプトベンゼン、1,4−ジメルカプトベンゼン、1,3− ビス( メルカプトメチル)ベンゼン、1,4−ビス(メルカプトメチル)ベンゼン、2,2’−ジメルカプトビフェニル、4、4’−ジメルカプトビフェニル、ビス(4−メルカプトフェニル)メタン、2,2−ビス(4−メルカプトフェニル)プロパン、ビス(4−メルカプトフェニル)エーテル、ビス(4−メルカプトフェニル)スルフィド、ビス(4−メルカプトフェニル)スルホン、ビス(4−メルカプトメチルフェニル)メタン、2,2−ビス(4−メルカプトメチルフェニル)プロパン、ビス(4−メルカプトメチルフェニル)エーテル、ビス(4−メルカプトメチルフェニル)スルフィド、、2,5−ジメルカプト−1,3,4−チアジアゾール、3,4−チオフェンジチオール、グリセリルジチオグリコーレート、2,5−ジメルカプト−1,3,4−チアジアゾール、1,3,5−トリアジン−2,4,6−トリチオール(トリメルカプト−トリアジン)、2−ジ−n−ブチルアミノ−4,6−ジメルカプト−s−トリアジン、ポリチオール( チオコール、またはチオール変性高分子(樹脂、ゴム等)が挙げられる。
錫系化合物としては、ジブチル錫ジクロライド、ジブチル錫オキサイド、ジブチル錫ジブロマイド、ジブチル錫ジマレエート、ジブチル錫ジラウレート(別名:DBTDL)、ジブチル錫ジアセテート、ジブチル錫スルファイド、トリブチル錫スルファイド、トリブチル錫オキサイド、トリブチル錫アセテート、トリエチル錫エトキサイド、トリブチル錫エトキサイド、ジオクチル錫オキサイド、トリブチル錫クロライド、トリブチル錫トリクロロアセテート、2−エチルヘキサン酸錫等が挙げられる。
非錫系化合物としては、例えばジブチルチタニウムジクロライド、テトラブチルチタネート、ブトキシチタニウムトリクロライドなどのチタン系、オレイン酸鉛、2−エチルヘキサン酸鉛、安息香酸鉛、ナフテン酸鉛などの鉛系、2−エチルヘキサン酸鉄、鉄2,4−ペンタジオネート、鉄アセチルアセトネートなどの鉄系、安息香酸酸コバルト、2−エチルヘキサン酸コバルトなどのコバルト系、ナフテン酸亜鉛、2−エチルヘキサン酸亜鉛などの亜鉛系、ナフテン酸ジルコニウムなどが挙げられる。
次にウレタンプレポリマー(C)、ウレタンウレアポリマー(C−1)について説明する。
ウレタンプレポリマー(C)は末端にイソシアネート基を有し、チオール基を導入するためのプレポリマーである。ウレタンプレポリマー(C)はポリオール(c−3)とポリイソシアネート(c−4)とをウレタン化反応させることによって得られるが、樹脂の凝集力を高めるためや、分子量の制御の観点から、さらにウレタンプレポリマー(C)にポリアミノ化合物(F)を反応させ、ウレア結合を導入したウレタンウレアポリマー(C−1)を用いることも出来る。ウレタンプレポリマー(C)、ウレタンウレアポリマー(C−1)の重量平均分子量(Mw)は特に限定されないが500〜200,000であることが好ましい。重量平均分子量が500未満であると接着剤としての凝集力が不足する場合があり、又、200,000を超えると接着剤組成物の粘度が高く、塗工性が悪化してしまう場合がある。塗工性と凝集力のバランスの観点で特に好ましくは1000〜100,000である。さらに好ましくは5000〜50,000である。
更に、ビスフェノールA やビスフェノールF 等のビスフェノール類にエチレンオキサイド等のアルキレンオキサイドを付加させたグリコール類も使用することができる。
多官能アルコール成分としては、例えば、上記した2 個または3 個の水酸基を有するポ
リオール類が挙げられ、中でも、後述の、式量60〜1000のポリオールが主に用いられる。
一般式(1):
−[−O−R1−O−CO−]m−
(式中、R1は2 価の有機残基、mは1以上の整数を表す。)
リコール、トリエチレングリコール、ブチレングリコール、3−メチル−1,5−ペンタンジオール、2−メチル−1,8−オクタンジオール、3,3’−ジメチロールヘプタン、ポリオキシエチレングリコール、ポリオキシプロピレングリコール、プロパンジオール、1,3−ブタンジオール、1,4−ブタンジオール、1,5−ペンタンジオール、1,6−ヘキサンジオール、1,9−ノナンジオール、ネオペンチルグリコール、オクタンジオール、ブチルエチルペンタンジオール、2−エチル−1,3−ヘキサンジオール、シクロヘキサンジオール;あるいはビスフェノールAやビスフェノールF等のビスフェノール類;ビスフェノール類にエチレンオキサイド、プロピレンオキサイド等のアルキレンオキサイドを付加させたビスフェノール類;等も用いることができる。これらの化合物は、1種又は2 種以上の混合物として使用することができる。
本発明のウレタンプレポリマー(C)の構成成分であるポリイソシアネート(c−4)としては、従来公知のものを使用することができ、芳香族ポリイソシアネート、脂肪族ポリイソシアネート、芳香脂肪族ポリイソシアネート、脂環族ポリイソシアネート等が挙げられる。
ポリイソシアネート(a−2)のうち、芳香族ポリイソシアネートとしては、より具体的に、例えば、1,3−フェニレンジイソシアネート、4,4’−ジフェニルジイソシアネート、1,4−フェニレンジイソシアネート、4,4’−ジフェニルメタンジイソシアネート(別名:4,4’−MDI)、2,4−トリレンジイソシアネート(別名:2,4−TDI)、2,6−トリレンジイソシアネート、4,4’−トルイジンジイソシアネート、2,4,6−トリイソシアネートトルエン、1,3,5−トリイソシアネートベンゼン、ジアニシジンジイソシアネート、4,4’−ジフェニルエーテルジイソシアネート、4,4’,4”−トリフェニルメタントリイソシアネート等を挙げることができる。
イソホロンジアミン、ジシクロヘキシルメタン−4,4’−ジアミン等の脂環式ポリアミン;
フェニレンジアミン、キシリレンジアミン、2,4−トリレンジアミン、2,6−トリレンジアミン、ジエチルトルエンジアミン,3,3’−ジクロロ−4,4’−ジアミノジフェニルメタン、4,4’−ビス−(sec−ブチル)ジフェニルメタン等の芳香族ジアミン;
及びダイマー酸のカルボキシル基をアミノ基に転化したダイマージアミン、末端に一級又は二級アミノ基を有するデンドリマーなどを例示できる。
一般式[2]:
H2N−CH2−CH2−CH2−O−(CmH2m−O)n−CH2−CH2−CH2−NH2
(式中、mは2〜4の任意の整数、nは2〜50の任意の整数を示す。)
次にα,β−不飽和二重結合基含有化合物(B)について説明する。
本発明に使用するα,β−不飽和二重結合基含有化合物(B)は、少なくとも一つ以上のα,β−不飽和二重結合基を有する化合物であり、後述する活性エネルギー線重合開始剤(G)により重合し、高分子量化及び架橋構造を形成することで接着剤に凝集力と高い耐久性を付与する。
例えば、(メタ)アクリル酸、(メタ)アクリル酸2−カルボキシエチル、(メタ)アクリル酸2−カルボキシプロピル、(メタ)アクリル酸3−カルボキシプロピル、(メタ)アクリル酸4−カルボキシブチル、(メタ)アクリル酸ダイマー、マレイン酸、フマル酸、モノメチルマレイン酸、モノメチルフマル酸、アコニチン酸、ソルビン酸、ケイ皮酸、α−クロロソルビン酸、グルタコン酸、シトラコン酸、メサコン酸、イタコン酸、チグリン酸、アンゲリカ酸、セネシオ酸、クロトン酸、イソククロトン酸、ムコブロム酸、ムコクロル酸、ソルビン酸、ムコン酸、アコニット酸、ペニシル酸、ゲラン酸、シトロネル酸、4−アクリルアミドブタン酸、6−アクリルアミドヘキサン酸、2−(メタ)アクリロイルオキシエチルサクシネート、モノ(メタ)アクリル酸ω−カルボキシポリカプロラクトンエステル等の、ラクトン環の開環付加によるカルボキシル基を末端に有する、ポリラクトン系(メタ)アクリル酸エステル、エチレンオキサイドやプロピレンオキサイド等のアルキレンオキサイドが繰り返し付加している、末端にカルボキシル基を有するアルキレンオキサイド付加系コハク酸と、(メタ)アクリル酸とのエステル等のカルボキシル基含有の脂肪族系α,β−不飽和二重結合基含有カルボン酸類やその酸無水物類;
4−ビニル安息香酸メチルポリ(エチレンオキサイド)、4−ビニル安息香酸エチルポリ(エチレンオキサイド)、4−イソプロペニル安息香酸メチルポリ(プロピレンオキサイド)、4−イソプロペニル安息香酸エチルポリ(プロピレンオキサイド)などのポリアルキレンオキサイド部位を有するビニル安息香酸エステル系またはイソプロペニル安息香酸エステル系単量体類;
2−メチル−2−プロペニルスルホン酸アンモニウム、2−メチル−2−プロペニルスルホン酸ナトリウム、2−メチル−2−プロペニルスルホン酸カリウム等の2−メチル−2−プロペニルスルホン酸の金属塩やアンモニウム塩類;
スチレンスルホン酸ナトリウム、スチレンスルホン酸カリウム、スチレンスルホン酸リチウム、スチレンスルホン酸マグネシウム、スチレンスルホン酸亜鉛、スチレンスルホン酸鉄等のスチレンスルホン酸の金属塩類;
ビニルオキシベンゼンスルホン酸アンモニウム、ビニルオキシベンゼンスルホン酸ナトリウム、ビニルオキシベンゼンスルホン酸カリウム等のアルケニル基含有ビニルオキシベンゼンスルホン酸の金属塩やアンモニウム塩類;
2−メチル−2−プロペニルオキシベンゼンスルホン酸アンモニウム、2−メチル−2−プロペニルオキシベンゼンスルホン酸ナトリウム、2−メチル−2−プロペニルオキシベンゼンスルホン酸カリウム等の2−メチル−2−プロペニルオキシベンゼンスルホン酸の金属塩やアンモニウム塩類等が挙げられる。
例えば、メチルビニルエーテル、エチルビニルエーテル、2−クロロビニルエーテル、n−プロピルビニルエーテル、アリルビニルエーテル、イソプロピルビニルエーテル、n−ブチルビニルエーテル、イソブチルビニルエーテル、イソブチルビニルエーテル、tert−ブチルビニルエーテル、n−ペンチルビニルエーテル、イソペンチルビニルエーテル、tert−ペンチルビニルエーテル、n−ヘキシルビニルエーテル、イソヘキシルビニルエーテル、2−エチルブチルビニルエーテル、2−エチルヘキシルビニルエーテル、n−ヘプチルビニルエーテル、n−オクチルビニルエーテル、イソオクチルビニルエーテル、ノニルビニルエーテル、デシルビニルエーテル、ドデシルビニルエーテル、ヘキサンデシルビニルエーテル、オクタデシルビニルエーテル、エトキシメチルビニルエーテル、2−メトキシエチルビニルエーテル、2−エトキシエチルビニルエーテル、2−ブトキシエチルビニルエーテル、アセトキシメチルビニルエーテル、2−アセトキシエチルビニルエーテル、3−アセトキシプロピルビニルエーテル、4−アセトキシブチルビニルエーテル、4−エトキシブチルビニルエーテル、2−(2−メトキシエトキシ)エチルビニルエーテル、3−ヒドロキシプロピルビニルエーテル、4−ヒドロキシブチルビニルエーテル、5−ヒドロキシペンチルビニルエーテル、6−ヒドロキシヘキシルビニルエーテル、ジエチレングリコールメチルビニルエーテル、ジエチレングリコールエチルビニルエーテル、ジエチレングリコールブチルビニルエーテルなどの脂肪族ビニルエーテル類;
本発明の接着剤組成物は、各種活性化エネルギー線の照射によって重合反応が進行し、硬化可能である。しかし、上記接着剤組成物は化合物(A)、化合物(B)の必須成分に加えて、必要に応じて活性エネルギー線重合開始剤(G)を含んでもよい。活性エネルギー線重合開始剤(G)を使用することによって、重合反応を促進することができる。本発明の一実施形態において、上記活性化エネルギーは紫外線であることが好ましく、紫外線の照射によって重合反応を進行させる場合、接着剤組成物は、活性エネルギー線重合開始剤(G)を含むことが好ましい。
具体例として、例えば、以下が挙げられる。4−フェノキシジクロロアセトフェノン、4−t−ブチル−ジクロロアセトフェノン、ジエトキシアセトフェノン、1−(4−イソプロピルフェニル)−2−ヒドロキシ−2−メチルプロパン−1−オン、1−ヒドロキシシクロヘキシルフェニルケトン、2−ベンジル−2−ジメチルアミノ−1−(4−モルフォリノフェニル)−ブタン−1−オン、2−メチル−1−[4−(メチルチオ)フェニル]−2−モルフォリノプロパン−1−オン等のアセトフェノン系開始剤、ベンゾイン、ベンゾインメチルエーテル、ベンゾインエチルエーテル、ベンゾインイソプロピルエーテル、ベンジルジメチルケタール等のベンゾイン系開始剤、ベンゾフェノン、ベンゾイル安息香酸、ベンゾイル安息香酸メチル、4−フェニルベンゾフェノン、ヒドロキシベンゾフェノン、アクリル化ベンゾフェノン、4−ベンゾイル−4’−メチルジフェニルサルファイド等のベンゾフェノン系開始剤、チオキサンソン、2−クロルチオキサンソン、2−メチルチオキサンソン、イソプロピルチオキサンソン、2,4−ジイソプロピルオキサンソン等のチオキサンソン系開始剤、2,4,6−トリクロロ−s−トリアジン、2−フェニル−4,6−ビス(トリクロロメチル)−s−トリアジン、2−(p−メトキシフェニル)−4,6−ビス(トリクロロメチル)−s−トリアジン、2−(p−トリル)−4,6−ビス(トリクロロメチル)−s−トリアジン、2−ピペロニル−4,6−ビス(トリクロロメチル)−s−トリアジン、2,4−ビス(トリクロロメチル)−6−スチリル−s−トリアジン、2−(ナフト−1−イル)−4,6−ビス(トリクロロメチル)−s−トリアジン、2−(4−メトキシ−ナフト−1−イル)−4,6−ビス(トリクロロメチル)−s−トリアジン、2,4−トリクロロメチル−(ピペロニル)−6−トリアジン、2,4−トリクロロメチル(4’−メトキシスチリル)−6−トリアジン等のトリアジン系開始剤、ボレート系開始剤、カルバゾール系開始剤、イミダゾール系開始剤等のラジカル発生剤が用いられる。
具体的な製品名としては例えば、イルガキュアー184,907,651,1700,1800,819,369,261、DAROCUR-TPO(BASF社製) 2,4,6−トリメチルベンゾイル−ジフェニル−フォスフィンオキサイド、ダロキュア-1173(メルク社製)、エザキュアーKIP150、TZT(日本シイベルヘグナー社製)、カヤキュアBMS、カヤキュアDMBI、(日本化薬社製)等が挙げられる。また、分子内に少なくとも1個の(メタ)アクリロイル基を有する光重合開始剤を使用することもできる。
その他の成分(H):
本発明の感圧式接着剤組成物には、本発明による効果を損なわない範囲であれば、各種添加剤(H)を適宜配合することも可能である。例えば、基材や、ガラス、金属箔、金属板(または鋼板)、又は金属蒸着フィルム等の無機材料表面への密着を向上させる場合はシランカップリング剤を使用することが効果的である。また、重合硬化収縮率低減、熱膨張率低減、寸法安定性向上、弾性率向上、粘度調整、熱伝導率向上、強度向上、靭性向上、及び着色向上等の観点から、有機又は無機の充填剤を配合することができる。このような充填剤は、ポリマー、セラミックス、金属、金属酸化物、金属塩、及び染顔料等の材料から構成されるものであってよい。また、その形状については、特に限定されず、例えば、粒子状及び繊維状等であってよい。なお、上記ポリマー系の材料を配合する場合には、チタネートカップリング剤、柔軟性付与剤、可塑剤、難燃化剤、保存安定剤、酸化防止剤、紫外線吸収剤、チクソトロピー付与剤、分散安定剤、流動性付与剤、色材及び消泡剤等の、独立した充填剤としてではなく、ポリマーブレンド又はポリマーアロイとして、樹脂組成物中に、溶解、半溶解又はミクロ分散させることも可能である。
次に、活性エネルギー線重合性接着剤組成物の性状について説明する。
本発明の活性エネルギー線重合性樹脂組成物は、上記、ウレタンポリマー(A)、α,β−不飽和二重結合基含有化合物(B)を必須成分とし、更に、必要に応じて、活性エネルギー線重合開始剤(G)やその他の成分(H)を配合後、均一に混合することによって製造することができる。攪拌・混合する際には、減圧装置を備えた1軸または多軸エクストルーダー、ニーダー、ディソルバーのような汎用の機器を使用し攪拌・混合することにより調製してもよい。攪拌・混合する際の温度は、通常、10〜60℃に設定されるのが好ましい。調製時の設定温度が10℃未満では、粘度が高すぎて均一な撹拌・混合作業が困難になる場合があり、逆に、調製時の温度が60℃を超えると、熱による硬化反応が起きる場合があり、正常な接着剤組成物が得られない場合があるので、好ましくない。
なお、本発明における活性エネルギー線重合性接着剤組成物は、有機溶剤を含まないことが好ましいが、有機溶剤を含有することも可能である。例えば、メタノール、エタノール、イソプロピルアルコール、アセトン、メチルエチルケトン、メチルイソブチルケトン、酢酸メチル、酢酸エチル、酢酸ブチル、シクロヘキサン、トルエン、キシレンその他の炭化水素系溶媒等の有機溶媒や、水をさらに添加して、接着剤組成物の粘度を調整することもできるし、接着剤組成物を加熱して粘度を低下させることもできる。
本発明の感接着剤組成物は、公知慣用の方法によって基材上に塗布することができ、次いで、形成された塗布層に活性エネルギー線を照射することによって、接着剤組成物の重合反応が進行し、硬化物を形成する。本発明の一実施形態において、活性エネルギー線は、紫外線を含む、150〜550nm波長域の光エネルギーを主体とすることが好ましい。このよう光エネルギーを提供する適切な光源として、例えば、低圧水銀灯、中圧水銀灯、高圧水銀灯、超高圧水銀灯、ケミカルランプ、ブラックライトランプ、マイクロウェーブ励起水銀灯、LEDランプ、キセノンランプ、及びメタルハライドランプなどが挙げられる。その他、本発明の別の実施形態では、レーザー光線、X線及び電子線などを露光用の活性エネルギー線として利用することもできる。
本発明の接着剤組成物は、好ましくは感圧式接着剤の用途で使用される。代表的に、感圧式接着剤組成物は、常法にしたがい適当な方法で基材の片面に塗工され、次いで重合硬化されることによって、接着層を形成する。この接着層をフィルム等の他の基材(E)に積層することにより様々な積層体を作成する。
各合成例で得られた樹脂組成物の液体外観を目視にて評価した。
数平均分子量(Mn)と重量平均分子量(Mw)の測定は、昭和電工社製GPC(ゲルパーミエーションクロマトグラフィー)「ShodexGPC System−21」を用いた。GPCは溶媒に溶解した物質をその分子サイズの差によって分離定量する液体クロマトグラフィーである。試料をテトラヒドロフランに溶解して、テトラヒドロフランを展開溶剤として流速を0.6ml/min、カラム温度を40℃の条件にて、測定した。標準物質としての単分散分子量のポリスチレンを使用した検量線を作成し、後述する合成例4〜18の分子量を、オリゴマー成分であるα,β−不飽和二重結合基含有化合物(D)を除いたポリスチレン換算の数平均分子量(Mn)、重量平均分子量(Mw)を測定した。
反応槽、滴下装置、攪拌機、温度計、還流冷却器、空気導入管を備えた重合反応装置の反応槽に、イソホロンジアミン(IPDA)40gを仕込み、そこにブチルアクリレート(BA)30.1gと4−ヒドロキシブチルアクリレート30.5gを混合した溶液を室温で滴下した。滴下終了後、80℃で4時間反応させた後、室温まで冷却させ反応を終了し、マイケル付加アミンを得た。
撹拌機、還流冷却管、窒素導入管、温度計、滴下ロートを備えた4口フラスコにPP2000(2官能ポリプロピレンポリオール、三洋化成工業株式会社製、数平均分子量:1000)526.8部、イソホロンジイソシアネート73.2部、触媒としてジオクチル錫ジラウレート0.05部を仕込み、100℃まで徐々に昇温して、2時間反応を行った。40℃まで冷却し、アセチルアセトン1.5部を加えた後、イソシアネート基残量を確認し、イソシアネート基残量と当モルのジブチルアミン8.5gを添加し、IRチャートのNCO特性吸収(2,270cm-1)が消失していることを確認し反応を終了した。このウレタン樹脂の重量平均分子量Mwは9,000であった。
撹拌機、還流冷却管、窒素導入管、温度計、滴下ロートを備えた4口フラスコにPP1000(2官能ポリプロピレンポリオール、三洋化成工業株式会社製、数平均分子量:1000)450部、イソホロンジイソシアネート150部、触媒としてジオクチル錫ジラウレート0.05部を仕込み、100℃まで徐々に昇温して、2時間反応を行った。40℃まで冷却し、アセチルアセトン1.5部を加えた後、イソシアネート基残量を確認し、イソシアネート基残量と当モルのアミノエタンチオール17.4gを添加し、再び昇温して100℃で30分反応させて、IRチャートのNCO特性吸収(2,270cm-1)が消失していることを確認し反応を終了した。このウレタン樹脂の重量平均分子量Mwは3,000であった。
撹拌機、還流冷却管、窒素導入管、温度計、滴下ロートを備えた4口フラスコにPP4000(2官能ポリプロピレンポリオール、三洋化成工業株式会社製、数平均分子量:4000)562.5部、イソホロンジイソシアネート37.5部、触媒としてジオクチル錫ジラウレート0.05部を仕込み、100℃まで徐々に昇温して、4時間反応を行った。40℃まで冷却し、イソシアネート基残量を確認し、イソシアネート基に対して0.5モルのアミノプロパンチオール1.28部を添加し、40℃で30分反応させた。その後さらにジブチルアミン(DBA)を1.82部添加し、IRチャートのNCO特性吸収(2,270cm-1)が消失していることを確認し反応を終了した。このウレタン樹脂の重量平均分子量Mwは22,000であった。
撹拌機、還流冷却管、窒素導入管、温度計、滴下ロートを備えた4口フラスコにポリエーテルポリオールPP−2000(2官能ポリプロピレンポリオール、三洋化成工業株式会社製、数平均分子量:2000)526.8部、イソホロンジイソシアネート(IPDI)73.2部、トルエン150部、触媒としてジブチル錫ジラウレート0.05部を仕込み、100℃まで徐々に昇温し2時間反応を行った。滴定でイソシアナト基残量を確認した後、40℃まで冷却、アセチルアセトン1.5部と酢酸エチル227部を加えた後、合成例1の化合物を11部を1時間で滴下し、さらに1時間熟成した後、イソシアネート基残量を確認し、イソシアネート基に対して1.0モルのアミノプロパンチオール0.9gを加えて、IRチャートのNCO特性吸収収(2,270cm-1)が消失していることを確認し反応を終了した。この反応溶液は無色透明で固形分50%、粘度3800cps、数平均分子量MN27,000、重量平均分子量MW110,000であった。
撹拌機、還流冷却管、窒素導入管、温度計、滴下ロートを備えた4口フラスコにポリエーテルポリオールPP−4000(2官能ポリプロピレンポリオール、三洋化成工業株式会社製、数平均分子量:4000)561部、イソホロンジイソシアネート(IPDI)39部、触媒としてジブチル錫ジラウレート0.05部を仕込み、100℃まで徐々に昇温し4時間反応を行った。滴定でイソシアナト基残量を確認した後、40℃まで冷却、イソホロンジアミン(IPDA)を1.5部を1時間で滴下し、さらに1時間熟成した後、イソシアネート基残量を確認し、イソシアネート基に対して0.5モルの2−アミノベンゼンチオール0.9部を加えて30分間反応させた。さらにジブチルアミン0.93gを加え、IRチャートのNCO特性吸収収(2,270cm-1)が消失していることを確認し反応を終了した。このウレタン樹脂 の重量平均分子量Mwは61,000であった。
PP2000:サンニックスPP−2000(2官能ポリプロピレングリコール、三洋化成工業社製、数平均分子量:2000)
PP1000:サンニックスPP−1000(2官能ポリプロピレングリコール、三洋化成工業社製、数平均分子量:1000)
IPDI:イソホロンジイソシアネート
・触媒
DOTDL:ジオクチル錫ジラウレート
IPDA:イソホロンジアミン
DBA:ジn−ブチルアミン
<接着剤組成物および積層体>
[実施例1〜6][比較例1〜2]
合成例2〜6で得られた樹脂組成物の溶液に、α,β−不飽和二重結合基含有化合物(B)及び各活性エネルギー線重合開始剤(G)を添加、混合し、均一な接着剤組成物の溶液とした。その後、得られた溶液を剥離処理されたポリエステルフィルム(厚さ38μm)(以下、「剥離性フィルム」という。)上に厚みが25μmになるようにコンマコーターにて速度2m/minで塗工し(溶剤を含むものについては100℃、2分の乾燥後の厚みが25μmとなるように塗工した)、次に得られた接着剤層に、活性エネルギー線照射装置(東芝社製 メタルハライドランプ)で最大照度500mW/cm2、積算光量800mJ/cm2の紫外線を照射し、重合硬化させて、50μm厚のポリエチレンテレフタレートフィルム(PETフィルム)を貼り合せて、感圧式接着剤フィルムを作製した。
上記感圧式接着剤フィルムを幅25mmに裁断し、剥離フィルムを剥がし、露出した感圧式接着剤層を厚さ1mmのガラス板に、23℃−50%RHの条件下で貼着し、JIS Z 0237に準じてロール圧着し、「ポリエステルフィルム/感圧式接着剤層/ガラス板」なる構成の積層体を作成した。圧着24時間後、剥離試験機にて剥離強度(180度ピール、引っ張り速度300mm/分;単位mN/25mm幅)を測定した。この剥離強度を粘着力として4段階で評価した。「△」評価以上の場合、実際の使用時に特に問題ない。
◎:粘着力が10.0(N/25mm)以上。
○:粘着力が5.0(N/25mm)以上〜10.0(N/25mm)未満。
△:粘着力が1.0(N/25mm)以上〜5.0(N/25mm)未満。
×:粘着力が1.0(N/25mm)未満。
上記感圧式接着剤フィルムを幅25mmに裁断し、剥離フィルムを剥がし、露出した感圧式接着剤層をステンレス板(SUS304)に、貼合わせ面積25mm×25mmとして貼合わせ、JISに準じてロール圧着し、80℃の環境下で20分放置後、その環境下にて1kgの重りをぶら下げ7万秒後の接着剤層の元の位置からのズレを次の3段階で評価した。
○:ズレが0〜1mm未満。
△:ズレが1mm〜25mm。
×:7万秒以内に被着体から落下
上記感圧式接着剤フィルムを幅25mmに裁断し、剥離フィルムを剥がし、J.Dow式ローリングボール法にて23℃、50%RHの条件下で測定し、次の3段階で評価した。
○:ボールタックが5〜12
△:ボールタックが3〜5
×:ボールタックが3未満
SR351:トリアクリル酸トリメチロールプロパン
SR454:エトキシ化トリアクリル酸トリメチロールプロパン(約3モル付加体)
LA:アクリル酸ラウリル
Claims (4)
- 末端の少なくとも1つにチオール基を有するウレタンポリマー(A)と、α,β−不飽和二重結合基含有化合物(B)とを必須成分とし、
前記ウレタンポリマー(A)が、末端にイソシアネート基を有するウレタンプレポリマー(C)にチオール基とアミノ基とを有する化合物(D)を反応させてなることを特徴とする活性エネルギー線重合性接着剤組成物。 - ウレタンプレポリマー(C)が、ウレア結合を含むウレタンウレアプレポリマー(C−1)である請求項1記載の活性エネルギー線重合性接着剤組成物。
- ウレタンポリマー(A)の重量平均分子量が、5000以上であることを特徴とする請求項1または2記載の活性エネルギー線重合性接着剤組成物。
- 基材(E)と、請求項1〜3いずれか記載の活性エネルギー線重合性接着剤組成物を含んでなる接着剤層とを有する積層体。
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