JP6402005B2 - 樹脂含有シート、並びに、それを用いた構造体および配線板 - Google Patents
樹脂含有シート、並びに、それを用いた構造体および配線板 Download PDFInfo
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- JP6402005B2 JP6402005B2 JP2014224603A JP2014224603A JP6402005B2 JP 6402005 B2 JP6402005 B2 JP 6402005B2 JP 2014224603 A JP2014224603 A JP 2014224603A JP 2014224603 A JP2014224603 A JP 2014224603A JP 6402005 B2 JP6402005 B2 JP 6402005B2
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- nonwoven fabric
- fixing agent
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Description
すなわち、微細な繊維からなる不織布、例えば、セルロースナノファイバー不織布においては、繊維同士が絡み合いや相互作用により集合体を形成している。よって、繊維の集合体に対し一方向に張力をかけると、繊維同士が接点で滑って引き離され、集合体にはほつれが生じ、最終的には破断することになる。
(1)セルロース微細繊維層を構成する繊維の比表面積相当繊維径が0.20μm以上1.0μm以下、
(2)透気抵抗度が1s/100ml以上40s/100ml以下、
(3)膜厚が8μm以上22μm以下、
前記セルロースナノファイバー不織布中の繊維同士を固着する固着剤と、
前記セルロースナノファイバー不織布と固着剤とに接する樹脂と、を有し、
前記固着剤の貯蔵弾性率が、前記樹脂の貯蔵弾性率よりも高いことを特徴とするものである。
図1に、本発明の樹脂含有シートの構造を示す説明図を示す。本発明の樹脂含有シートは、主として繊維成分と樹脂成分から形成されるシート状体であり、図示するように、セルロースナノファイバー不織布11と、セルロースナノファイバー不織布11中の繊維1同士を固着する固着剤2と、セルロースナノファイバー不織布11と固着剤2とに接する樹脂3と、を有している。なお、図中の符号Sは、セルロースナノファイバー不織布11内で固着剤2および樹脂3のいずれも含浸されていない空間を示す。本発明の樹脂含有シートにおいては、セルロースナノファイバー不織布11を構成する繊維1と、固着剤2と、樹脂3とが、全体として1つの層を形成しているものといえる。本発明の樹脂含有シートにおいては、繊維1同士を固着する固着剤2の貯蔵弾性率が、いずれかの温度において、樹脂3の貯蔵弾性率よりも高い点が重要である。
本発明の樹脂含有シートに用いるセルロースナノファイバー不織布は、再生セルロース微細繊維を70質量%以上含有するセルロース微細繊維層を少なくとも一層含む単層または3層以下の複数層から構成される。好ましくは、再生セルロース微細繊維は75質量%以上である。再生セルロース微細繊維が70質量%未満となると、樹脂の含浸性の観点から好ましくない。
比表面積=4/(dD) (m2/g)
を誘導した。BET法による比表面積を上式の比表面積として代入し、セルロース密度としてd=1.50g/cm3を代入することにより繊維径Dに換算した数値を、比表面積相当繊維径と定義する。ここで、BET法による比表面積測定は、比表面積・細孔分布測定装置(ベックマン・コールター社製)にて、試料約0.2gに対する液体窒素の沸点における窒素ガスの吸着量を同装置のプログラムに則り測定した後、比表面積を算出することにより行った。
W0=100×W
次に、セルロース微細繊維の製造方法について記載する。セルロース繊維の微細化は、再生セルロース繊維および天然セルロース繊維ともに、前処理工程、叩解処理工程および微細化工程を経ることが好ましい。特に、再生セルロース繊維を微細化する場合には、前処理工程は油剤を除去するための、場合によって界面活性剤を使用する水洗工程にて実施できるが、天然セルロース繊維の前処理工程においては、100〜150℃の温度での水中含浸下でのオートクレーブ処理、酵素処理等、またはこれらの組み合わせによって、原料パルプが以降の工程で微細化し易い状態にしておくことは有効である。上記前処理工程の際に、1質量%以下の濃度の無機酸(塩酸、硫酸、リン酸、ホウ酸など)ないしは有機酸(酢酸、クエン酸など)を添加してオートクレーブ処理を行うことも、場合によっては有効である。これらの前処理は、微細化処理の負荷を軽減するだけでなく、セルロース繊維を構成するミクロフィブリルの表面や間隙に存在するリグニンやヘミセルロース等の不純物成分を水相へ排出し、その結果、微細化された繊維のα−セルロース純度を高める効果もあるため、セルロースナノファイバー不織布の耐熱性の向上に大変有効であることもある。
固着剤2を形成する固着剤組成物としては、セルロースナノファイバー不織布11中の繊維1に付着して、繊維1同士を固着させることができるものであればよく、繊維同士が互いに接し合う接点部のみを固着するものであっても、繊維1の全体を被覆して固着するものであってもよい。固着剤組成物の使用量としては、繊維1同士を固着させることができ、耐屈曲性に悪影響が及ばない程度の量であればよく、繊維1を固着剤2により固着させた集合体において、有機溶媒を除いた固形分で、繊維1と固着剤2との体積比が99:1〜50:50の範囲、特には、99:1〜60:40の範囲であることが好ましい。繊維1と固着剤2との体積比がこの範囲であると、繊維1同士が固着剤により十分に固着されて所望の高強度が得られるものとなるとともに、その後の樹脂3の含浸により良好な耐屈曲性が確保できるものとなり、好ましい。特には、固着剤2の使用量は、固着剤2の適用前後において、セルロースナノファイバー不織布11の膜厚が実質的に変化しない程度の量であることが好ましい。ここで、膜厚が実質的に変化しないとは、セルロースナノファイバー不織布11が固着剤組成物の溶剤成分等により膨潤して見かけ上厚みを増すような場合を膜厚の変化に含まないとの意味である。また、固着剤組成物は、繊維に付着させる際に液体であることが好ましく、温度や圧力を変えることで液体にして用いることができるものであってもよい。特には、固着剤組成物の、25℃にてE型粘度計におけるローター回転数5rpmで測定した粘度が1Pa・s以下、例えば、1〜0.0001Pa・sであることが好ましく、これにより、繊維1の集合体の内部まで、固着剤組成物を含浸させることができ、繊維同士を、より確実に固着させることができる。
熱硬化性樹脂は、加熱により硬化して電気絶縁性を示す樹脂であればよく、例えば、ビスフェノールA型エポキシ樹脂、ビスフェノールF型エポキシ樹脂、ビスフェノールS型エポキシ樹脂、ビスフェノールE型エポキシ樹脂、ビスフェノールM型エポキシ樹脂、ビスフェノールP型エポキシ樹脂、ビスフェノールZ型エポキシ樹脂などのビスフェノール型エポキシ樹脂、ビスフェノールAノボラック型エポキシ樹脂、フェノールノボラック型エポキシ樹脂、クレゾールノボラックエポキシ樹脂などのノボラック型エポキシ樹脂、ビフェニル型エポキシ樹脂、ビフェニルアラルキル型エポキシ樹脂、アリールアルキレン型エポキシ樹脂、テトラフェニロールエタン型エポキシ樹脂、ナフタレン型エポキシ樹脂、アントラセン型エポキシ樹脂、フェノキシ型エポキシ樹脂、ジシクロペンタジエン型エポキシ樹脂、ノルボルネン型エポキシ樹脂、アダマンタン型エポキシ樹脂、フルオレン型エポキシ樹脂、グリシジルメタアクリレート共重合系エポキシ樹脂、シクロヘキシルマレイミドとグリシジルメタアクリレートとの共重合エポキシ樹脂、エポキシ変性のポリブタジエンゴム誘導体、CTBN変性エポキシ樹脂、トリメチロールプロパンポリグリシジルエーテル、フェニル−1,3−ジグリシジルエーテル、ビフェニル−4,4’−ジグリシジルエーテル、1,6−ヘキサンジオールジグリシジルエーテル、エチレングリコールまたはプロピレングリコールのジグリシジルエーテル、ソルビトールポリグリシジルエーテル、トリス(2,3−エポキシプロピル)イソシアヌレート、トリグリシジルトリス(2−ヒドロキシエチル)イソシアヌレート、フェノールノボラック樹脂、クレゾールノボラック樹脂、ビスフェノールAノボラック樹脂などのノボラック型フェノール樹脂、未変性のレゾールフェノール樹脂、桐油、アマニ油、クルミ油などで変性した油変性レゾールフェノール樹脂などのレゾール型フェノール樹脂などのフェノール樹脂、フェノキシ樹脂、尿素(ユリア)樹脂、メラミン樹脂などのトリアジン環含有樹脂、不飽和ポリエステル樹脂、ビスマレイミド樹脂、ジアリルフタレート樹脂、シリコーン樹脂、ベンゾオキサジン環を有する樹脂、ノルボルネン系樹脂、シアネート樹脂、イソシアネート樹脂、ウレタン樹脂、ベンゾシクロブテン樹脂、マレイミド樹脂、ビスマレイミドトリアジン樹脂、ポリアゾメチン樹脂、ポリイミド樹脂等が挙げられる。これらの中でも特に、エポキシ樹脂やポリイミド樹脂が、絶縁層としての信頼性が優れているために好ましい。
光硬化性樹脂としては、活性エネルギー線の照射により硬化して電気絶縁性を示す樹脂であればよく、特には、分子中に1個以上のエチレン性不飽和結合を有する化合物が好ましく用いられる。エチレン性不飽和結合を有する化合物としては、公知慣用の光重合性オリゴマーおよび光重合性ビニルモノマー等が用いられる。
本発明の樹脂含有シートにおいて、樹脂3は、固着剤2とセルロースナノファイバー不織布11とに接するものである。本発明において、樹脂3は、弾性や耐屈曲性を阻害しない程度であればよく、セルロースナノファイバー不織布11の外側を被覆していてもよい。樹脂組成物の含浸率としては、樹脂含有シートの貯蔵弾性率や耐屈曲性を阻害しない程度であれば特に限定はないが、樹脂含有シート中の樹脂の濃度として、10〜99体積%、特には、10〜70体積%であることが好ましい。樹脂組成物の含浸率を上記範囲内とすることで、良好な耐屈曲性と、高強度とをバランス良く得ることができる。
熱可塑性樹脂としては、アクリル、変性アクリル、低密度ポリエチレン、高密度ポリエチレン、エチレン−酢酸ビニル共重合体、ポリエチレンテレフタレート、ポリプロピレン、変性ポリプロピレン、ポリスチレン、アクリロニトリル−ブタジエン−スチレン共重合体、アクリロニトリル−スチレン共重合体、酢酸セルロース、ポリビニルアルコール、ポリ塩化ビニル、ポリ塩化ビニリデン、ポリ乳酸等の汎用プラスチック類、ポリアミド、熱可塑性ポリウレタン、ポリアセタール、ポリカーボネート、超高分子量ポリエチレン、ポリブチレンテレフタレート、変性ポリフェニレンエーテル、ポリスルホン(PSF)、ポリフェニレンスルファイド(PPS)、ポリエーテルスルホン(PES)、ポリエーテルエーテルケトン、ポリアリレート、ポリエーテルイミド、ポリアミドイミド、液晶ポリマー、ポリアミド6T、ポリアミド9T、ポリテトラフロロエチレン、ポリフッ化ビニリデン、ポリエステルイミド、熱可塑性ポリイミド等のエンジニアリングプラスチック類、オレフィン系、スチレン系、ポリエステル系、ウレタン系、アミド系、塩化ビニル系、水添系等の熱可塑性エラストマーが挙げられる。本発明においては、樹脂複合体を使用することもでき、例えば、熱硬化性樹脂と熱可塑性樹脂の樹脂複合体として、エポキシ樹脂−PSF、エポキシ樹脂−PPS、エポキシ樹脂−PES等が使用できる。
本発明においては、固着剤2の貯蔵弾性率が、樹脂3の貯蔵弾性率よりも高いことが必要である。ここで、固着剤2の貯蔵弾性率とは、繊維1は含まずに、固着剤組成物の成分のみの配合物を、成膜後に熱または光により硬化させた硬化膜の貯蔵弾性率を意味する。同様に、樹脂3の貯蔵弾性率についても、硬化性樹脂の場合には成膜後に熱または光により硬化させた硬化膜の貯蔵弾性率を意味し、熱可塑性樹脂の場合には、溶融成膜後に溶剤を除去して得られる塗膜の貯蔵弾性率を意味する。また、貯蔵弾性率とは、試料の硬さの一指標値であって、一定の温度変化を加えながら試料に対し周期的な荷重をかけて歪を検出する動的粘弾性測定と呼ばれる評価を行って、検出した歪から算出される値であり、この値が高いほど優れた力学強度を示していることを意味する。本発明においては、いずれかの温度において、固着剤2の貯蔵弾性率が樹脂3の貯蔵弾性率よりも高いものであればよく、その好適範囲は、固着剤2の貯蔵弾性率については30〜0.1GPaであり、より好ましくは20〜0.5GPaであり、樹脂3の貯蔵弾性率については10〜0.001GPaであり、より好ましくは5〜0.01GPaであり、いずれかの温度において、固着剤2の貯蔵弾性率が樹脂3の貯蔵弾性率よりも0.1GPa以上大きいことが好ましい。特には、150〜250℃の範囲内のいずれかの温度において、固着剤2の貯蔵弾性率が、樹脂3の貯蔵弾性率よりも高いことが好ましく、150〜250℃の全温度範囲において、固着剤2の貯蔵弾性率が、樹脂3の貯蔵弾性率よりも高いことがより好ましい。これにより、本発明の樹脂含有シートは、150〜250℃の高温領域でも使用可能となるので、用途が広がることから、好ましい。
本発明においては、固着剤2のガラス転移温度が、樹脂3のガラス転移温度または軟化温度よりも高いことが好ましい。ここで、固着剤2のガラス転移温度とは、繊維1は含まずに、固着剤組成物の成分のみの配合物を、成膜後に熱または光により硬化させた硬化膜のガラス転移温度を意味する。同様に、樹脂3のガラス転移温度または軟化温度についても、硬化性樹脂の場合には成膜後に熱または光により硬化させた硬化膜のガラス転移温度を意味し、熱可塑性樹脂の場合には、溶融成膜後に溶剤を除去して得られる塗膜の軟化温度を意味する。また、ガラス転移温度とは、前述の動的粘弾性測定から得られた貯蔵弾性率(E′)と損失弾性率(E″)の比(E″/E′)から算出される値(損失正接)が最大のときの温度のことであり、この温度が高いほど優れた耐熱性を示していることを意味する。本発明においては、ガラス転移温度の上限については特に制限されないが、その好適範囲は、固着剤2のガラス転移温度については130℃以上であり、より好ましくは140℃以上であり、樹脂3のガラス転移温度または軟化温度については70℃以上であり、より好ましくは80℃以上であり、固着剤2のガラス転移温度が樹脂3のガラス転移温度または軟化温度よりも5℃以上大きいことが好ましい。
本発明の樹脂含有シートは、セルロースナノファイバー不織布11を固着剤組成物で処理して繊維1同士を固着させた後、固着されたセルロースナノファイバー不織布11に樹脂組成物を含浸することにより、得ることができる。本発明の樹脂含有シートは、例えば、キャリアフィルム等の被塗布物上に繊維を配置した状態で、固着剤組成物および樹脂組成物を順次塗布、含浸させて、固着剤組成物および樹脂組成物中に含まれる有機溶媒を揮発乾燥することにより、ドライフィルムとして製造することもでき、所望に応じ、さらに、その上にカバーフィルムを貼り合わせてもよい。この際、樹脂組成物が、固着剤組成物の繊維に対する固着性能を阻害するものでなければ、樹脂組成物の塗布プロセスは、固着剤の乾燥前であっても乾燥後であっても、いずれでもよい。
窒素置換させた攪拌機付属の三つ口フラスコに、脱水N−メチル−2−ピロリドン(NMP)溶媒(和光純薬工業(株)製)を入れ、4,4’−ジアミノジフェニルエーテル(ODA)(和光純薬工業(株)製)と1,2,4,5−ベンゼンテトラカルボン酸二無水物(PMDA)(和光純薬工業(株)製)とを1:1のモル比で配合し、室温で16時間以上撹拌して、樹脂固形分割合が7.5質量%であるポリアミック酸ワニス1を得た。
窒素置換させた攪拌機付属の三つ口フラスコに、脱水N−メチル−2−ピロリドン(NMP)溶媒(和光純薬工業(株)製)を入れ、p−フェニレンジアミン(PDA)(和光純薬工業(株)製)と、3,3’,4,4’−ビフェニルテトラカルボン酸無水物(BPDA)(和光純薬工業(株)製)とを1:1のモル比で配合し、室温で16時間以上撹拌して、樹脂固形分割合が7.5質量%であるポリアミック酸ワニス2を得た。
下記表1中に、固着剤組成物または樹脂組成物として使用される組成物1〜4の配合内容を示す。下記表1中の組成物1〜4の記載に従い、各組成物を調製した。組成物1の複数成分系の場合は、各成分を配合した後、自転・公転ミキサーを用いて攪拌し、調製した。
各組成物1〜4をそれぞれ、厚さ18μmの銅箔にアプリケーターを用いて塗布し、塗膜を得た。
組成物1については、熱風循環式乾燥炉で80℃、30分間の大気条件下で乾燥後、150℃、60分間の大気条件下で加熱させてエポキシ樹脂硬化物を得た。銅箔を除去したところ、厚みは50μmであった。この硬化物を用いて、幅5mm、長さ50mmの貯蔵弾性率等評価用試験片を作製した。
組成物2については、塗布後、熱風循環式乾燥炉で80℃、30分間の大気条件下で乾燥後、250℃、60分間の窒素条件下(100ml/min.)で加熱してイミド化物を得た。銅箔を除去したところ、厚みは50μmであった。その後、上記と同様にして評価用試験片を作製した。
組成物3については、加熱操作を300℃、60分間の窒素条件下で行った以外は組成物2と同様にして評価用試験片を作製した。
組成物4については、高密度ポリエチレンペレット(比重0.95)をプレス機に適量投入して、140℃、3MPa、3分間加熱加圧後、室温まで冷却して成形体を得た後に個片化したところ、厚みは50μmであった。その後、上記と同様にして評価用試験片を作製した。
下記表2中に、各実施例および比較例の樹脂含有シートないしシートの構成を示す。
双日(株)により入手した再生セルロース繊維であるテンセルカット糸(3mm長)を洗浄用ネットに入れて界面活性剤を加え、洗濯機で何度も水洗することにより、繊維表面の油剤を除去した。得られた精製テンセル繊維(カット糸)を固形分1.5質量%となるように水中に分散させて(400L)、ディスクレファイナー装置として相川鉄工(株)製SDR14型ラボリファイナー(加圧型DISK式)を用い、ディスク間のクリアランスを1mmで400Lの該水分散体を20分間叩解処理した。それに引き続き、クリアランスをほとんどゼロに近いレベルにまで低減させた条件下で叩解処理を続けた。経時的にサンプリングを行い、サンプリングスラリーに対して、JIS P 8121で定義されるCSF値を評価したところ、CSF値は経時的に減少していき、一旦、ゼロ近くとなった後、さらに叩解処理を続けると、増大していく傾向が確認された。クリアランスをゼロ近くとしてから約14時間、上記条件で叩解処理を続け、CSF値で15ml↑の叩解水分散体(固形分濃度:1.5質量%)を得た。得られた叩解水分散体を、そのまま高圧ホモジナイザー(ニロ・ソアビ社(伊)製NS015H)を用いて操作圧力100MPa下で1回および5回の微細化処理を実施し、それぞれ微細セルロース繊維の水分散体M1およびM2(固形分濃度:共に1.5質量%)を得た。
下記表2中の実施例1については、上記セルロースナノファイバー不織布を用いて、ここに、上記組成物1(粘度0.0005Pa・s)を含浸させた後、熱風循環式乾燥炉で80℃、30分間の大気条件下で乾燥後、150℃、60分間で加熱硬化させて、セルロースナノファイバー不織布および固着剤(エポキシ樹脂組成物の硬化物)からなる中間体を作製した。
下記表2中の実施例2については、実施例1と同様のセルロースナノファイバー不織布に、上記組成物2(粘度0.001Pa・s)を含浸させた後、熱風循環式乾燥炉で80℃、30分間の大気条件下で乾燥後、250℃、60分間で加熱してイミド化し、セルロースナノファイバー不織布および固着剤(ポリイミド)からなる中間体を作製した。
下記表2中の実施例3については、実施例1と同様のセルロースナノファイバー不織布に、上記組成物3(粘度0.001Pa・s)を含浸させた後、熱風循環式乾燥炉で80℃、30分間の大気条件下で乾燥後、300℃、60分間で加熱してイミド化し、セルロースナノファイバー不織布および固着剤(ポリイミド)からなる中間体を作製した。
実施例1と同様に、上記組成物1を使用してセルロースナノファイバー不織布および固着剤(エポキシ樹脂組成物の硬化物)からなる中間体を作製した。
実施例1については、上記組成物4をプレス機に投入して、140℃で溶融させた後に、上記で得られた各中間体に含浸させ、140℃、3MPa、3分間加熱加圧後、室温まで冷却させることで、固着剤(エポキシ樹脂組成物)で固着されたセルロースナノファイバー不織布に、樹脂(高密度ポリエチレン樹脂)が含浸された樹脂含有シートを作製した。
固着剤または樹脂の貯蔵弾性率等評価用試験片を用いて、DMA粘弾性測定装置((株)日立ハイテクサイエンス製 DMA7100)の引張モードを用い、測定周波数1Hz、最小張力および最小圧縮力200mN、歪振幅10μm、昇温速度5℃/分、大気下条件で粘弾性を測定し、50℃、150℃および250℃における貯蔵弾性率を得るとともに、ガラス転移温度または軟化温度を得た。その結果を下記表1に示す。
樹脂含有シートまたはシート評価用試験片については、シート中のセルロースナノファイバー不織布またはアラミド不織布の繊維のバイアス(斜め)方向が装置の引張方向となるように試験片を取り付け、最小張力および圧縮力を50mNとした以外は、上記と同様にして粘弾性を測定し、50℃、150℃および250℃における貯蔵弾性率を得た。ここで、バイアス(斜め)方向に測定するのは、セルロースナノファイバー不織布そのものの弾性率の影響を極力排除し、固着効果による弾性率向上の影響を調べるためである。各実施例については、固着剤を付着させていない比較例のシートと比べたとき、貯蔵弾性率E[GPa]の値が大きい場合は〇、小さい場合は×とした。
セルロースナノファイバー不織布をキャリアフィルム上に配置したこと以外は、上記と同様にして固着剤組成物を塗布、含浸させて、各中間体を作製した。その後、乾燥後の固着剤の表面に、樹脂組成物を成形または塗布し、乾燥させた後、カバーフィルムを貼り合わせて、ドライフィルムを得た。このドライフィルムの両面に厚み18μmの表面未処理銅箔を重ね合わせて(密着させる際にキャリアフィルムおよびカバーフィルムは剥離した)、真空プレス機で、加圧条件を1MPa、加熱条件を、実施例1については150℃×10分、実施例2、比較例4については250℃×60分、実施例3については300℃×60分として成形し、樹脂層と銅箔とが密着した耐屈曲性評価用試験片を作製した。また、比較例1〜3については、固着剤組成物を塗布、含浸しないこと以外は同様にドライフィルムを作製、真空プレス機で加圧し、比較例1〜3のシート作製と同様の温度条件で耐屈曲性評価用試験片を作製した。
耐屈曲性評価用試験片を用いて、屈曲半径0.8mm、屈曲速度175回/分、折り曲げ角度135°、荷重200g、樹脂層が内側になる向きに曲げて、屈曲試験を行った。試験片が破断するまでの折り曲げ回数が100回以上の場合を〇、70〜99回を△、69回以下を×とした。その結果を下記表2に示す。評価結果が〇である場合、耐屈曲性に優れるといえる。
2 固着剤
3 樹脂
11 セルロースナノファイバー不織布
S 空間
Claims (6)
- 再生セルロース微細繊維を70質量%以上含有するセルロース微細繊維層を少なくとも一層含む単層または3層以下の複数層から構成され、下記(1)〜(3)のすべての要件を満足するセルロースナノファイバー不織布と、
(1)セルロース微細繊維層を構成する繊維の比表面積相当繊維径が0.20μm以上1.0μm以下、
(2)透気抵抗度が1s/100ml以上40s/100ml以下、
(3)膜厚が8μm以上22μm以下、
前記セルロースナノファイバー不織布中の繊維同士を固着する固着剤と、
前記セルロースナノファイバー不織布と固着剤とに接する樹脂と、を有し、
前記固着剤の貯蔵弾性率が、前記樹脂の貯蔵弾性率よりも高いことを特徴とする樹脂含有シート。 - 前記固着剤のガラス転移温度が、前記樹脂のガラス転移温度または軟化温度よりも高い請求項1記載の樹脂含有シート。
- 前記セルロースナノファイバー不織布の繊維同士を固着剤組成物により固着させた後、該固着されたセルロースナノファイバー不織布に樹脂組成物を含浸して得られる請求項1または2記載の樹脂含有シート。
- 前記固着剤組成物の粘度が1Pa・s以下である請求項3記載の樹脂含有シート。
- 請求項1〜4のうちいずれか一項記載の樹脂含有シートを、基板に密着させて得られることを特徴とする構造体。
- 請求項5記載の構造体を有することを特徴とする配線板。
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EP15857169.5A EP3216823B1 (en) | 2014-11-04 | 2015-10-28 | Resin-containing sheet, and structure and wiring board using same |
CN201580060047.XA CN107075155B (zh) | 2014-11-04 | 2015-10-28 | 含树脂片材、以及使用其的结构体和电路板 |
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US15/523,504 US10047202B2 (en) | 2014-11-04 | 2015-10-28 | Resin-containing sheet, and structure and wiring board using same |
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