JP2005154589A - シートモールディングコンパウンド及びバルクモールディングコンパウンド用樹脂組成物、及びその応用 - Google Patents
シートモールディングコンパウンド及びバルクモールディングコンパウンド用樹脂組成物、及びその応用 Download PDFInfo
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- JP2005154589A JP2005154589A JP2003395456A JP2003395456A JP2005154589A JP 2005154589 A JP2005154589 A JP 2005154589A JP 2003395456 A JP2003395456 A JP 2003395456A JP 2003395456 A JP2003395456 A JP 2003395456A JP 2005154589 A JP2005154589 A JP 2005154589A
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- acrylate
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Abstract
【解決手段】 1分子中にエチレン性不飽和二重結合を有する樹脂(A)と、エチレン性不飽和二重結合を有する単量体(B)と、ヒドラジン、尿素等の化合物、β−ジケトン化合物等及びパーオキサイド化合物からなる群から選ばれる少なくとも1種の化合物(C)とを含有してなるシートモールディングコンパウンド及びバルクモールディングコンパウンド用樹脂組成物、シートモールディングコンパウンド及びバルクモールディングコンパウンド、及びその成形品に関する。
【選択図】 なし
Description
これら成形品を得るための、シートモールディングコンパウンド(SMC)やバルクモールディングコンパウンド(BMC)には、通常、ラジカル硬化剤が含有されており、併せて含有される重合性不飽和二重結合を有する重合性不飽和樹脂と、重合性不飽和単量体とを反応させ硬化物を得るが、この際、ホルムアルデヒドが発生することが知られている(例えば非特許文献1参照)。
Stanford Research Institute Volume1 Number 7 July,1968; Frank R. Mayo
本発明における、1分子中にエチレン性不飽和二重結合を有する樹脂(A)[以下ラジカル硬化性樹脂(A)という]としては、例えば不飽和ポリエステル、エポキシ(メタ)アクリレート、ウレタン(メタ)アクリレート、ポリエステル(メタ)アクリレート、分子鎖末端に重合性不飽和結合基を含有するマクロモノマー等が挙げられる。これらの樹脂の数平均分子量は300より大きいものであるが、樹脂の粘度や樹脂硬化物の物性の点で500〜5000のものが好ましい。これらの樹脂は、単独で使用しても良いし、必要に応じ、2種以上併用しても良い。
かかるエポキシ樹脂としては、平均エポキシ当量が、100〜500なる範囲内のも
のが好ましく、具体的には以下に例示される化合物が挙げられる。
R7−NH−Y (3)
R7がアルキル基であり、かつYが−CO−NH−を含む1価の官能基である一般式(1)で表される化合物(C)としては、例えば尿素、モノメチル尿素、モノメチロール尿素、ジメチロール尿素、ジメチル尿素、ジフェニル尿素、メチレン尿素、エチレン尿素、プロピレン尿素、アルコシキメチル尿素等が挙げられる。これらのうち、ホルムアルデヒド捕捉効果の大きい点でエチレン尿素が好ましい。
さらにR7がウレタン結合を有する1価の官能基であり、かつYが−COO−を含む1価の官能基を有する化合物(C)としては、ウレタン(メタ)アクリレート等のビニルウレタン化合物等が挙げられる。
するものである。
有機繊維の場合、具体的にはアラミド、ナイロン、ビニロン、ポリエステル、フェノール樹脂等が挙げられる。その形態としては、織物状のマット等が挙げられるが特に限定されるものではない。繊維強化材を使用する場合の配合量は、樹脂組成物、あるいは成形材料全量に対して、2〜50重量部配合することが可能である。
かかる添加剤としては、低収縮化剤の分離防止剤または相溶化剤、減粘剤あるいは粘度低減剤と呼ばれるもの等があり、その添加量としては、ラジカル硬化性樹脂(A)と重合性不飽和単量体(B)との合計100重量部に対して、好ましくは0.1〜10重量部である。
前記製造法で使用されるフィルムとしては、ポリエチレンフィルム、ポリプロピレンフィルム、ポリエチレンテレフタレートフィルム、ナイロン等のポリアミドフィルム、あるいはこれらを用いた積層フィルム等が挙げられる。フィルムは、単独で使用しても、2種以上併用して用いても良い。
均一に混合するための混合装置としては、例えば攪拌機、プラネタリーミキサー、ニーダー、レジゲミキサー、ロールミル、スクリュ−押出式混練機等の装置を用いることが好ましい。
<製造例1>(不飽和ポリエステル樹脂組成物)
無水マレイン酸392部と、ネオペンチルグリコール208部、プロピレングリコール171部とを脱水縮合反応して不飽和ポリエステル樹脂を得、スチレン含量40重量%の不飽和ポリエステル樹脂とした。この不飽和ポリエステル樹脂組成物をラジカル硬化性樹脂組成物aという。この不飽和ポリエステル樹脂の酸価は15であった。
<製造例2>(不飽和ポリエステル樹脂組成物)
無水マレイン酸294部と、イソフタル酸166部、ネオペンチルグリコール208部、プロピレングリコール167.2部とを脱水縮合反応して不飽和ポリエステルを得、スチレン含量40重量%の不飽和ポリエステル樹脂組成物とした。この樹脂組成物をラジカル硬化性樹脂組成物bという。この不飽和ポリエステル樹脂の酸価は14であった。
<製造例3>(エポキシメタクリレート樹脂組成物)
エポキシ当量410のビスフェノールA型のエポキシ樹脂620部とメタクリル酸124部とを反応してエポキシメタクリレートを得、スチレン含量38重量%のエポキシメタクリレート樹脂組成物とした。このエポキシメタクリレートをラジカル硬化性樹脂組成物cという。
製造例1〜3に示した樹脂組成物A、B及びC、低収縮化剤、無機充填材、顔料、禁止剤、重合開始剤、離型剤、増粘剤、ガラス繊維、化合物(C)(以下ホルムアルデヒド補捉剤という)を用い、表−1および表−2に示された実施例および比較例の配合比率のSMCを公知の製造方法によって製造した。
この際、低収縮化剤は、ポリスチレンのスチレン溶液(スチレン含量65%)を用いた。
充填材は、平均粒子径6μmの水酸化アルミニウム、及びまたは平均粒子径3μmの炭酸カルシウムを用いた。
また顔料は、酸化チタン系顔料を用い、剥離剤としてオレフィン系化合物を用い、重合開始剤は、t−ブチルパーオキシベンゾエート(TBPB)、またはt−ブチルパーオキシイソプロピルカーボネート(TBPIPC)を用いた。また離型剤は、ステアリン酸亜鉛(Zn−St)を用い、増粘剤は、酸化マグネシウムを用い、繊維補強材は、ガラス繊維を用いた。
前記SMC成形材料を145℃、10MPaの条件下で8分間加熱圧縮成形し、厚み5mmの成形品を得た。この成形品を試験片として、成形性、曲げ強さ、曲げ弾性率、ホルムアルデヒド放散量について、観察および確認した結果を表−1および表−2に示した。
実施例6及び比較例5
製造例2に示した樹脂、重合開始剤、増粘剤、ホルムアルデヒド補捉剤、ガラス繊維を用い、表−3に示された実施例および比較例の配合比率のSMCを公知の製造方法によって製造した。この際、重合開始剤としては、50%濃度のt−ブチルパーオキシ2エチルヘキサノエート(TBPEH)を、増粘剤としては、酸化マグネシウムを、繊維補強材としては、ガラス繊維を使用した。
前記SMC成形材料を70〜80℃、0.1MPaの条件下で4時間加熱圧縮成形し、厚み5mmの成形品を得た。
[試験方法及び評価基準]
この成形品の成形性、曲げ強さ、曲げ弾性率、ホルムアルデヒド放散量について、観察および確認した結果を表−3に示した。
SMC成形材料のフィルム剥ぎ性については、前記で得られたSMC成形材料を成形する前に、フィルムに挟み込まれている材料を取り出す際、材料がベタつかない場合を○、ベタつく場合を×とした。
<成形性>
成形性については、前記SMC成形材料を成形する際、離型不良等の問題が起こるか否かを見た。成形時に離型不良が起こらない場合を○とした。
<曲げ強さ、弾性率>
得られた成形品より試験片を切り出し、JIS−K 7203に準拠して測定した。
<ホルムアルデヒド放散量>
得られた成形品から15cm×15cmの試験片を2枚切り出し、JIS K 5601−4−1デシケーター法に準拠して測定した。成形品は温度23℃、湿度50%の環境試験室内(4m×4m×2m)で1日間の養生を行った。
Claims (7)
- 1分子中にエチレン性不飽和二重結合を有する樹脂(A)と、エチレン性不飽和二重結合を有する単量体(B)と、分子中にヒドラゾ基、尿素結合又はウレタン結合のいずれかの官能基を有する化合物、一般式(1)で表される化合物及び一般式(2)で表される化合物からなる群から選ばれる少なくとも1種の化合物(C)とラジカル重合開始剤(D)とを含有してなるシートモールディングコンパウンド及びバルクモールディングコンパウンド用樹脂組成物。
- 前記分子中にヒドラゾ基、尿素結合又はウレタン結合のいずれかの官能基を有する化合物が、一般式(3)で表される化合物である請求項1記載の樹脂組成物。
R7−NH−Y (3)
(式中、R7は、水素原子、アルキル基、アルケニル基、アルキニル基、水酸基で置換されたアルキル基、アミノ基で置換されたアルキル基、アルコキシ基で置換されたアルキル基、アミノ基、フェニル基、カルボキシル基、ウレタン結合を有する1価の官能基及び−NHNH−R8を表す。但しR8は、水素原子又はアルキル基である。Yは−NH−、−CO−NH−又は−COO−を含む1価の官能基を表す。またR7とYとは結合して環を形成していてもよい。 ) - 前記一般式(3)で表される化合物が、エチレン尿素である請求項1又は2記載の樹脂組成物。
- 前記一般式(1)で表される化合物が、アセトアセトキシエチル(メタ)アクリレートである請求項1記載の樹脂組成物。
- 請求項1〜4のいずれかに記載の樹脂組成物と繊維強化材とを配合してなるシートモールディングコンパウンド。
- 請求項1〜4のいずれかに記載の樹脂組成物と繊維強化材とを配合してなるバルクモールディングコンパウンド。
- 請求項5又は6記載のコンパウンドを成形してなる成形品。
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005162920A (ja) * | 2003-12-04 | 2005-06-23 | Showa Highpolymer Co Ltd | ラジカル重合性樹脂組成物硬化体の製造方法 |
JP6241583B1 (ja) * | 2016-10-11 | 2017-12-06 | Dic株式会社 | 繊維強化成形材料及びそれを用いた成形品 |
WO2018070076A1 (ja) * | 2016-10-11 | 2018-04-19 | Dic株式会社 | 繊維強化成形材料及びそれを用いた成形品 |
JP2019085508A (ja) * | 2017-11-08 | 2019-06-06 | Dic株式会社 | 繊維強化成形材料及びそれを用いた成形品 |
WO2019142803A1 (ja) * | 2018-01-16 | 2019-07-25 | 三菱ケミカル株式会社 | マトリクス樹脂、中間材及び成形品 |
WO2021095688A1 (ja) * | 2019-11-12 | 2021-05-20 | ジャパンコンポジット株式会社 | 不飽和ポリエステル樹脂組成物、成形材料および成形品 |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0597945A (ja) * | 1991-04-25 | 1993-04-20 | Showa Highpolymer Co Ltd | 不飽和ポリエステル樹脂組成物 |
JPH09110949A (ja) * | 1995-10-17 | 1997-04-28 | Kayaku Akzo Kk | 不飽和ポリエステル樹脂又はビニルエステル樹脂用硬化剤組成物及び硬化方法 |
JPH11130881A (ja) * | 1997-10-31 | 1999-05-18 | Hitachi Chem Co Ltd | 加飾用プリプレグシート及び繊維強化プラスチック成形体の製造方法 |
JPH11197501A (ja) * | 1998-01-07 | 1999-07-27 | Nippon Synthetic Chem Ind Co Ltd:The | アルデヒド吸着剤及びその用途、その使用方法 |
JP2002293847A (ja) * | 2001-01-24 | 2002-10-09 | Rp Topla Ltd | 不飽和ポリエステル樹脂組成物およびそれからなる成形品 |
JP2005036176A (ja) * | 2003-06-25 | 2005-02-10 | Japan Composite Co Ltd | 樹脂組成物の硬化方法 |
-
2003
- 2003-11-26 JP JP2003395456A patent/JP4780369B2/ja not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0597945A (ja) * | 1991-04-25 | 1993-04-20 | Showa Highpolymer Co Ltd | 不飽和ポリエステル樹脂組成物 |
JPH09110949A (ja) * | 1995-10-17 | 1997-04-28 | Kayaku Akzo Kk | 不飽和ポリエステル樹脂又はビニルエステル樹脂用硬化剤組成物及び硬化方法 |
JPH11130881A (ja) * | 1997-10-31 | 1999-05-18 | Hitachi Chem Co Ltd | 加飾用プリプレグシート及び繊維強化プラスチック成形体の製造方法 |
JPH11197501A (ja) * | 1998-01-07 | 1999-07-27 | Nippon Synthetic Chem Ind Co Ltd:The | アルデヒド吸着剤及びその用途、その使用方法 |
JP2002293847A (ja) * | 2001-01-24 | 2002-10-09 | Rp Topla Ltd | 不飽和ポリエステル樹脂組成物およびそれからなる成形品 |
JP2005036176A (ja) * | 2003-06-25 | 2005-02-10 | Japan Composite Co Ltd | 樹脂組成物の硬化方法 |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005162920A (ja) * | 2003-12-04 | 2005-06-23 | Showa Highpolymer Co Ltd | ラジカル重合性樹脂組成物硬化体の製造方法 |
JP6241583B1 (ja) * | 2016-10-11 | 2017-12-06 | Dic株式会社 | 繊維強化成形材料及びそれを用いた成形品 |
WO2018070076A1 (ja) * | 2016-10-11 | 2018-04-19 | Dic株式会社 | 繊維強化成形材料及びそれを用いた成形品 |
US10669386B2 (en) | 2016-10-11 | 2020-06-02 | Dic Corporation | Fiber-reinforced molding material and molded article using same |
JP2019085508A (ja) * | 2017-11-08 | 2019-06-06 | Dic株式会社 | 繊維強化成形材料及びそれを用いた成形品 |
JP7003583B2 (ja) | 2017-11-08 | 2022-01-20 | Dic株式会社 | 繊維強化成形材料及びそれを用いた成形品 |
WO2019142803A1 (ja) * | 2018-01-16 | 2019-07-25 | 三菱ケミカル株式会社 | マトリクス樹脂、中間材及び成形品 |
JPWO2019142803A1 (ja) * | 2018-01-16 | 2020-01-23 | 三菱ケミカル株式会社 | マトリクス樹脂、中間材及び成形品 |
WO2021095688A1 (ja) * | 2019-11-12 | 2021-05-20 | ジャパンコンポジット株式会社 | 不飽和ポリエステル樹脂組成物、成形材料および成形品 |
CN114555664A (zh) * | 2019-11-12 | 2022-05-27 | 日本复合材料株式会社 | 不饱和聚酯树脂组合物、成型材料及成型品 |
WO2023054575A1 (ja) * | 2021-09-29 | 2023-04-06 | 三菱ケミカル株式会社 | プリプレグを製造する方法およびプリプレグ |
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