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JPH0244710B2 - - Google Patents
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JPH0244710B2 - - Google Patents

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Publication number
JPH0244710B2
JPH0244710B2 JP62212173A JP21217387A JPH0244710B2 JP H0244710 B2 JPH0244710 B2 JP H0244710B2 JP 62212173 A JP62212173 A JP 62212173A JP 21217387 A JP21217387 A JP 21217387A JP H0244710 B2 JPH0244710 B2 JP H0244710B2
Authority
JP
Japan
Prior art keywords
evoh
boric acid
weight
experimental example
layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP62212173A
Other languages
Japanese (ja)
Other versions
JPS6372544A (en
Inventor
Yukio Ooseki
Kyoichiro Igari
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kuraray Co Ltd
Original Assignee
Kuraray Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kuraray Co Ltd filed Critical Kuraray Co Ltd
Priority to JP62212173A priority Critical patent/JPS6372544A/en
Publication of JPS6372544A publication Critical patent/JPS6372544A/en
Publication of JPH0244710B2 publication Critical patent/JPH0244710B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はエチレン・ビニルアルコール共重合体
樹脂(以下EVOHという)とアルコール系可塑
剤及びホウ酸又はホウ酸塩から成る耐衝撃性及び
成形性の良好な樹脂組成物を用いた多層容器に関
するものである。容器は食品、有機薬品、農薬、
ガソリン等のプラスチツク製包装容器で、該樹脂
組成物を少くとも一層含む多層構造を有し、ガス
遮断性、耐有機溶剤性がすぐれており、且つ耐衝
撃性、良好な成形性を備えたプラスチツク製多層
容器に関するものである。 例えば従来農薬等の薬品用容器としてはガラス
製が用いられて来たが破損し易く、取扱い時に危
険を伴なうし、又容器自体重いために運搬等の作
業にも不便であつた。これに対応して、プラスチ
ツク製容器として特開昭53−61478、特開昭53−
61479に示されるようにナイロン系の樹脂を内層
とした多層容器が開発されたが、ナイロン系の樹
脂は耐溶剤性が充分でなく、充填された薬品が壁
面を透過し内容物が減少する次点があつた。 また特開昭54−72271に示された如く、エチレ
ン・ビニルアルコール樹脂を内層とした容器を作
成すると、ナイロン系樹脂を使用した容器よりは
るかにすぐれた耐溶剤性を示し、内容物の透過減
量は殆んど起らない。しかし、EVOH樹脂は耐
衝撃性が十分でなく、ボトルの落下強度が低い欠
点がある。EVOHはすぐれた耐薬品性、耐気体
透過性、耐有機蒸気透過性などのバリアー性を有
するため、これらの特性を生かして種々の分野に
使用されるが、耐衝撃性が低いため制約をうける
ことが多い。この点を改良するため従来種々の可
塑剤が検討され、たとえば特開昭47−17850(N−
N−ジ低級アルキルホルムアミド2〜40重量部を
配合して成ることを特徴とする熱可塑性樹脂組成
物)、特開昭47−17851(スルホキシド化合物2〜
40重量部を配合して成ることを特徴とする熱可塑
性樹脂組成物)、特開昭51−20946(オルガノシリ
コン化合物0.01〜10重量部を混合することを特徴
とする製造方法)、特開昭53−37756〔3−メチル
ペンタン−1,3,5−トリオールおよび/又は
2−(2−ヒドロオキシプロピル)プロパン−1,
3−ジオールとよりなる組成物〕、特公昭50−
20979(多価アルコールとグリシジルエーテルを等
モル比の割合で付加せしめて得られる反応生成物
2〜40重量部配合して成る熱可塑性樹脂組成物)
等が知られている。 また樹脂をダイより垂直に下方にパイプ状に押
出した時に自重によつてパイプの厚さが薄くなり
伸びてしまう現象をドローダウン性というが、
EVOHは本質的にこの傾向が大きく、単層ある
いは多層での中空成形に際して成形不能あるいは
著しい偏肉を生じ易く製造工程上問題となること
が多い。また耐衝撃性を改良するために可塑剤を
配合するとドローダウン性は更に不良となる。従
つて、可塑剤を配合したEVOHを使用すれば耐
衝撃性は向上するが、ドローダウン性のため成形
品の不良品率が大きくなる欠点があつた。他の多
くの樹脂の場合には、分子量を増加させることに
よつてドローダウン性を減少させ得るが、
EVOHの場合分子量を大きくしてドローダウン
性を小さくすることが難しい。 本発明者らは、先にEVOHの耐衝撃性を改良
し、且つドローダウン性等の成形性もすぐれた組
成物を得るべく種々検討した。その結果エチレン
含有量25〜50モル%、ケン化度96%以上の
EVOHにアルコール系可塑剤の特定量とホウ酸
又はホウ酸塩の特定量とを配合させることにより
耐衝撃性を著しく改良するだけでなく、ドローダ
ウン性の低下を抑えて成形性をも向上させ得るこ
とを見出し、かゝる組成物に関する特許出願をし
た(特願昭55−109924)。更にその性能を改善す
るため製造方法について種々検討した結果、その
配合の順序と成形物の物性は密接な関係があり、
最初にホウ酸またはホウ酸塩をアルコール系可塑
剤に充分溶解せしめた後、EVOHと混合(たと
えば混練)することにより、一層耐衝撃性及びド
ローダウン性が改善されることを見出し、本発明
に到達した。更にこのようにして得られた
EVOH樹脂組成物を少くとも一層として用いた
共押出法によつて製造した多層ボトルは該樹脂層
の偏肉も少なく、落下強度も大であること、又同
様に該樹脂層を少くとも一層に用いた共押出シー
トの深しぼり成形品も偏肉が少なく、且つ落下強
度も大なることを見出したものである。 すなわち、エチレン含有率25〜60モル%、ケン
化度96%以上のエチレン・ビニルアルコール共重
合体樹脂100重量部、アルコール系可塑剤2〜15
重量部及びホウ酸またはホウ酸塩0.05〜3重量部
からなり、かつホウ酸またはホウ酸塩はアルコー
ル系可塑剤に溶解された後、エチレン・ビニルア
ルコール共重合体樹脂と混合せしめられてなる樹
脂組成物の層を少くとも一層含む耐衝撃性がすぐ
れた多層容器である。 以下本発明を更に詳しく説明する。 本発明に使用されるEVOHのエチレン含有率
は25〜60モル%の間にあることが必要であり、エ
チレン含有率が25モル%以下になると成形温度が
分解温度に近くなり成形が困難となる。エチレン
含有率が60モル%以上になるとEVOHの優れた
耐油性などが低下し、また軟化点も低下してくる
から各種の応用が期待できない。 またケン化度は96モル%以下になると耐油性、
耐気体透過性が低下し、不適当である。 また本発明において使用に適しているEVOH
の分子量は広い範囲にわたつているが、フエノー
ル85重量%と水15重量%とからなる30℃の混合溶
剤を用いて測定した極限粘度〔η〕が0.05〜0.15
/gの範囲に相当する分子量が好ましい。〔η〕
が0.05以下では成形品の機械的強度も低下し、本
発明による耐衝撃性の改良が困難となる。〔η〕
が0.15以上では、樹脂の粘性が高すぎて可塑剤と
の均一な配合及びホウ酸やホウ酸塩配合によるド
ローダウン性の改良効果が十分でない。 本発明に用いる可塑剤としてのアルコール系可
塑剤はEVOHに対する相溶性が良好で可塑効果
が充分であるばかりでなく、ホウ酸又はホウ酸塩
その併用に当つて成形のし易さ、目的とする効果
を得るために重要な撰択である。またホウ酸又は
ホウ酸塩はポリビニルアルコールのゲル化剤とし
て知られているが、アルコール系可塑剤との特定
量を共用且つ特定の順序でEVOHに配合させた
樹脂組成物とすることに依つて始めてドローダウ
ン性を小さく、成形性良好で、耐衝撃性が十分で
ありかつ優れた耐溶剤性、耐油性を備えた樹脂組
成物の製造が可能となる。 本発明に用いられるアルコール系可塑剤として
はグリセリン、ジグリセリン、12プロパンジオー
ル、1,3プロパンジオール、1,2ブタンジオ
ール、1,3ブタンジオール、2,3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、3メチルペンタン1,3,5トリオー
ル、2,5ヘキサンジオール、1,2,6ヘキサ
ントリオール、ジエタノールアミン、トリエタノ
ールアミン、ジエチレングリコール、2−(2−
ヒドロオキシプロピル)プロパン1,3ジオール
等を用いることができる。可塑剤の配合率は2〜
15重量%の間にあることが必要であり、2重量部
以下では樹脂組成物の耐衝撃性が十分でなく、15
重量部以上ではホウ酸又はホウ酸塩配合によるド
ローダウン性の改良効果が期待できず、又15重量
部を越えるとEVOHとの良好な相溶状態がくず
れてブリードが激しくなり成形物にべとつきが生
じる。アルコール系可塑剤の配合割合は、4〜8
重量%が特に好ましい。 ドローダウン性改良のための配合剤としては、
アルコール系可塑剤及びEVOH樹脂に均一なゲ
ル化効果を与えるホウ酸又はホウ酸塩が適当であ
る。こゝでホウ酸塩とは含水四ホウ酸ナトリウ
ム、無水四ホウ酸ナトリウム、その他ナトリウム
以外のホウ酸塩をいう。尚ドローダウン性低下は
ホウ酸またはホウ酸塩のゲル化効果によると考え
られる。その他ゲル化剤として有機過酸化物、多
価イソシアネート、多官能性エポキシ化合物、多
価カルボン酸等があげられるが、これらはドロー
ダウン性及び耐衝撃性を同時に満足させることが
できず、また成形品の表面荒れが生じ易い。 ホウ酸又はホウ酸塩の配合率は0.05〜3重量部
であることが必要である。0.05重量部以下ではド
ローダウン性が不良であつて本発明の効果が認め
られず、又3重量部以上ではゲル化がすすみすぎ
たり、均一な反応が行なわれず、成形品の表面荒
れ、偏肉等の問題を生じる。このような観点から
ホウ酸又はホウ酸塩の添加量は0.15〜1.0重量部
が特に好ましい。 アルコール系可塑剤及びホウ酸又はホウ酸塩を
EVOHに配合する場合、その順序は極めて重要
である。すなわち、最初にアルコール系可塑剤に
ホウ酸又はホウ酸塩を充分に溶解した後、
EVOHと混合(たとえば混練)する必要がある。
いゝかえればEVOH樹脂とホウ酸又はホウ酸塩
とがアルコール系可塑剤の介在なしに接触するこ
とは避けねばならない。即ち本発明の配合順序に
従つた時にのみ耐衝撃性を改良し、成形性も良好
な組成物を製造し得るのであつて、最初にホウ酸
とEVOHを接触させた場合には、耐衝撃性の向
上効果に著しいばらつきを生ずるだけでなく、成
形品の偏肉、成形品表面の肌荒れを生じたりす
る。この原因は明らかではないが、EVOHの水
酸基とホウ酸又はホウ酸塩との反応に先立つてア
ルコール系可塑剤の水酸基とホウ酸又はホウ酸塩
との反応を生ぜしめた後、その反応生成物が
EVOH樹脂と作用することにより本発明の目的
が達せられるものと考えられる。これは可塑剤と
してアルコール系可塑剤を用いた時にのみホウ酸
又はホウ酸塩との相互作用で本発明の目的を達す
る点からも推定される。アルコール系可塑剤を含
まない系ではホウ酸又はホウ酸塩とEVOH樹脂
が局所的ゲル化を生じて不均一になるというよう
な単純な物理的効果では説明され得ない現象であ
る。 具体的な配合方法としては、ホウ酸またはホウ
酸塩60〜80℃に加温したアルコール系可塑剤に加
えて撹拌し、充分に溶解した後、EVOHを一定
の比率で押出機に加え、混練してペレツト化する
方法が最も適当である。 本発明の多層容器とは前述した方法により得た
組成物の層を少くとも一層に有し、その他ポリオ
レフイン、ポリアミド、ポリエステル、ボリ塩化
ビニル等の熱可塑性樹脂あるいは必要に応じてこ
れらに充てん剤を加えた組成物の層を一層または
複数層を有し、必要ならばこれらの間に接着層を
有する中空成形容器である。またシートより深し
ぼりによつて加工された成形容器、射出成形容器
を含むが、特に本発明の成形性改良の効果は中空
成形容器の製造に最も適している。これらの熱可
塑性樹脂層はEVOH組成物層の保護層であり、
水の影響、強度、透湿性などを勘案し、適宜選択
される。この場合加工法としては共押出法に依る
のが普通である。また容器の成形時1軸または2
軸延伸法を併用することも可能である。該
EVOH組成物の層、すなわち、バリアー層は、
内層、中間層、外層のいずれにあつてもよく、偏
肉の少く、耐衝撃性が高いため破損のおそれがな
く、内容物、例えば有機薬剤の壁面透過による減
量のおそれがない容器を提供しうる。 本発明に用いる組成物には必要に応じて防曇
剤、酸化防止剤、アルコール系以外の可塑剤、着
色剤、充填剤等を添加することもできる。 本発明の多層容器は本来のすぐれた耐薬品性、
バリアー性機能を有するだけでなく、EVOH樹
脂の欠点である落下強度を改良して偏肉なしに効
率よく製造できるため、従来品では使用困難であ
つた分野にも適用しうる。たとえば各種有機薬剤
や農薬、昇華性薬品、ガソリンなぞどの石油類、
更に酸化防止を目的とした食用油脂、みそなど食
品用中空瓶、硬質深しぼり成形品などに用い得
る。その他、耐油性を必要とする自動車の部品等
にも使用しうる。 次に実施例を掲げて本発明を更に具体的に説明
するが、これら実施例によつて本発明は何ら限定
されるものではない。尚実験例、実施例、比較実
験例、比較例における試験及び評価方法は次のと
おりである。また可塑剤及びホウ酸又はホウ酸
(含ホウ酸塩)の添加量はEVOH重量に対する比
率で示した。 1 MI ASTM−D−1238に従い、メルトインデク
サーを使用して2160Kgの荷重をかけた時の10分
間の樹脂の流量を示す。測定温度は190℃であ
る。 2 アイゾツト衝撃強度 ASTM−D−256に従いノツチ付の衝撃強度
を示す。 試料は射出成型により作成し、(厚さ、巾は
1/2インチ×1/2インチ)ノツチを1/10インチ入
れたものを20℃、65%RHで1週間放置した
後、20℃、65%RHで測定した。 3 落下テスト 20℃、65%RHにおいてブロー容器(容量
500c.c.)に500c.c.の水を充填した直後にフタをし
て、高さを変更してコンクリート床面上に垂直
に落下させる。各々の高さにおいて、最高同じ
ボトルを10回落下させ、壊れなかつた回数を示
す。10ケのボトルを使用してその平均値を求め
四捨五入して整数とする。 4 内容物減少量 ブロー容器(容量500c.c.)にキシレンを500c.c.
入れ、50℃において1ケ月放置して重量変化を
測定した。 5 ボトルの偏肉性 ボトル胴部の厚み斑によつて下記のように示
した。 三層ボトルの場合には必要な層を剥離してボ
トル胴部の厚さ斑をダイヤルゲージで測定し
た。 偏肉性小…平均厚みに対して 0〜±10%の厚
み斑 中…平均厚みに対して ±10〜±30%の厚
み斑 大…平均厚みに対して ±30〜±50%の厚
み斑 実験例 1 エチレン含有率30モル%、ケン化度99.5モル
%、〔η〕が0.10/gのEVOHを40mmφ押出機
へ仕込むに際して、ホツパー口からジエチレング
リコールに、ジエチレングリコールに対して7.5
重量%のホウ酸を予め溶解せしめた溶液を滴下し
つつペレツト化を行ない、ジエチレングリコール
8重量%、ホウ酸0.6重量%を含有するEVOH組
成物の試料を得た。 これを用いて射出成型を行ないIzod衝撃試験用
サンプルを採取し、衝撃強度を測定した。次にこ
のペレツトを用いて40mmφ押出機により径20mmの
パイプ状で下向きに樹脂を押出し、パイプの先端
から3cm及び10cmの部分の厚みを測定した。 結果を表1に示す。 比較実験例 1 実験例1において使用したEVOHを用いて、
ホウ酸とEVOHペレツトをドライブレンドしこ
れを40mmφ押出機によつて混練ペレツト化してホ
ウ酸0.6重量%を含有するEVOHペレツトを作成
した。その後実験例1と同様にしてジエチレング
リコールをホウ酸含有EVOHペレツトに配合し
て最終的に実験例1と同様なジエチレングリコー
ル8重量%、ホウ酸0.6重量%を含有するEVOH
組成物の試料を得た。これについて実験例1に示
したと同様なテストを行なつた。結果を表1に示
す。 比較実験例 2 実験例1において使用したEVOHに実験例1
と同様にしてジエチレングリコールを配合した。
この配合ペレツトとホウ酸をドライブレンドして
比較実験例1と同様に混練ペレツト化し、最終的
に実験例1と同様なジエチレングリコール8重量
%、ホウ酸0.6重量%を含有するEVOH組成物の
試料を得た。これについて実験例1に示したと同
様なテストを行なつた。結果を表1に示す。 比較実験例 3 実験例1で使用したEVOHのみを用いて実験
例1に示したと同様なテストを行なつた。結果を
表1に示す。 比較実験例 4 実験例1において使用したEVOHを40mmφ押
出機へ仕込むに際して、ジエチレングリコールに
対して40重量%のホウ酸を予め溶解せしめた溶液
を滴下しつつ、ペレツト化を行ない、ジエチレン
グリコール8重量%、ホウ酸3.2重量%を含有す
るEVOH組成物の試料を得た。 これについて実験例1に示したと同様なテスト
を行なつた。結果を表1に示す。 実験例 2 エチレン含有率45モル%、ケン化度99.5モル
%、〔η〕が0.09/gのEVOHを40mmφ押出機
へ仕込むに際して、ホツパー口からグリセリン
に、グリセリンに対して10重量%の含水四ホウ酸
ナトリウムを予め溶解せしめた溶液を滴下しつ
つ、ペレツト化を行ない、グリセリン10重量%、
含水四ホウ酸ナトリウム1.0重量%を含有する
EVOH組成物を得た。これについて、実験例1
に示したと同様なテストを行なつた。結果を表2
に示す。 比較実験例 5 実験例2において使用したEVOHを用いて、
四ホウ酸ナトリウムとEVOHペレツトをドライ
ブレンドし、これを40mmφ押出機によつて混練ペ
レツト化して四ホウ酸ナトリウム1.0重量%を含
有するEVOHペレツトを作成した。その後、実
験例1と同様にしてグリセリンを四ホウ酸ナトリ
ウム含有EVOHペレツトに配合して最終的に実
験例2と同様なグリセリン10重量%、ホウ酸1.0
重量%を含有するEVOH組成物の試料を得た。
これについて実験例1に示したと同様なテストを
行なつた。結果を表2に示す。 比較実験例 6 実験例2において使用したEVOHに実験例2
と同様にしてグリセリンを配合した。この配合ペ
レツトと四ホウ酸ナトリウムをドライブレンドし
て比較実験例5と同様に混練ペレツト化し、最終
的に実験例2と同様なグリセリン10重量%、ホウ
酸1.0重量%を含有するEVOH組成物の試料を得
た。これについて実験例1に示したと同様なテス
トを行なつた。結果を表2に示す。 比較実験例 7 実験例2で使用したEVOHのみを用いて実験
例1に示したと同様なテストを行なつた。結果を
表2に示す。
The present invention relates to a multilayer container using a resin composition with good impact resistance and moldability consisting of an ethylene-vinyl alcohol copolymer resin (hereinafter referred to as EVOH), an alcohol plasticizer, and boric acid or a borate salt. be. Containers can be used for foods, organic chemicals, pesticides,
A plastic packaging container for gasoline, etc., which has a multilayer structure containing at least one layer of the resin composition, and has excellent gas barrier properties and organic solvent resistance, as well as impact resistance and good moldability. The invention relates to a multi-layered container. For example, glass containers have conventionally been used for chemicals such as agricultural chemicals, but they are easily damaged and dangerous when handled, and the containers themselves are heavy, making them inconvenient for transportation. In response to this, plastic containers were developed in JP-A-53-61478 and JP-A-53-61478.
As shown in No. 61479, a multilayer container with an inner layer of nylon resin was developed, but the nylon resin did not have sufficient solvent resistance, and the chemicals filled in the container permeated through the wall and the contents were reduced. The dot was hot. Furthermore, as shown in JP-A-54-72271, when containers are made with an ethylene/vinyl alcohol resin as the inner layer, they exhibit much better solvent resistance than containers made of nylon resin, and the amount of permeation of the contents is reduced. rarely occurs. However, EVOH resin does not have sufficient impact resistance and has the drawback of low bottle drop strength. EVOH has excellent barrier properties such as chemical resistance, gas permeation resistance, and organic vapor permeation resistance, so it is used in a variety of fields by taking advantage of these properties, but it is limited by its low impact resistance. There are many things. In order to improve this point, various plasticizers have been studied in the past, such as JP-A-47-17850 (N-
Thermoplastic resin composition characterized by containing 2 to 40 parts by weight of N-di-lower alkylformamide), JP-A-17851-1985 (Sulfoxide compound 2 to 40 parts by weight)
Thermoplastic resin composition characterized by mixing 40 parts by weight), JP-A-51-20946 (Production method characterized by mixing 0.01 to 10 parts by weight of an organosilicon compound), JP-A-Sho 51-20946 (Production method characterized by mixing 0.01 to 10 parts by weight of an organosilicon compound) 53-37756 [3-methylpentane-1,3,5-triol and/or 2-(2-hydroxypropyl)propane-1,
Composition consisting of 3-diol], Special Publication 1977-
20979 (Thermoplastic resin composition comprising 2 to 40 parts by weight of a reaction product obtained by adding polyhydric alcohol and glycidyl ether in an equimolar ratio)
etc. are known. Also, when resin is extruded vertically downward from a die into a pipe shape, the pipe becomes thinner and stretches due to its own weight, which is called drawdown property.
EVOH inherently has this tendency, and when blow molding a single layer or multiple layers, it tends to be impossible to mold or cause significant thickness deviation, which often causes problems in the manufacturing process. Furthermore, if a plasticizer is added to improve the impact resistance, the drawdown property becomes even worse. Therefore, if EVOH mixed with a plasticizer is used, the impact resistance is improved, but there is a drawback that the reject rate of molded products increases due to the drawdown property. For many other resins, drawdown can be reduced by increasing molecular weight;
In the case of EVOH, it is difficult to increase the molecular weight and reduce the drawdown property. The present inventors have previously conducted various studies to improve the impact resistance of EVOH and to obtain a composition with excellent moldability such as drawdown property. As a result, the ethylene content was 25 to 50 mol%, and the degree of saponification was 96% or more.
By blending EVOH with a specific amount of alcohol-based plasticizer and a specific amount of boric acid or borate, it not only significantly improves impact resistance, but also improves moldability by suppressing the drop in drawdown properties. He discovered that it could be obtained, and filed a patent application for such a composition (Japanese Patent Application No. 109924/1983). Furthermore, as a result of various studies on manufacturing methods to improve its performance, we found that there is a close relationship between the order of compounding and the physical properties of the molded product.
It has been discovered that impact resistance and drawdown properties can be further improved by first sufficiently dissolving boric acid or a boric acid salt in an alcohol-based plasticizer, and then mixing (for example, kneading) with EVOH. Reached. Furthermore, it was obtained in this way
A multilayer bottle manufactured by a coextrusion method using an EVOH resin composition as at least one layer has less uneven thickness of the resin layer and has high drop strength. It was discovered that the deep-drawn molded product of the coextruded sheet used also has less uneven thickness and has high drop strength. That is, 100 parts by weight of an ethylene/vinyl alcohol copolymer resin with an ethylene content of 25 to 60 mol% and a degree of saponification of 96% or more, and an alcoholic plasticizer of 2 to 15%.
part by weight and 0.05 to 3 parts by weight of boric acid or a boric acid salt, and the boric acid or boric acid salt is dissolved in an alcohol plasticizer and then mixed with an ethylene-vinyl alcohol copolymer resin. This is a multilayer container with excellent impact resistance that includes at least one layer of the composition. The present invention will be explained in more detail below. The ethylene content of EVOH used in the present invention must be between 25 and 60 mol%; if the ethylene content is less than 25 mol%, the molding temperature will approach the decomposition temperature, making molding difficult. . When the ethylene content exceeds 60 mol%, EVOH's excellent oil resistance and other properties deteriorate, and its softening point also decreases, making it difficult to expect various applications. In addition, when the degree of saponification is 96 mol% or less, oil resistance
Gas permeability is reduced, making it unsuitable. EVOH also suitable for use in the present invention
Although its molecular weight varies over a wide range, the intrinsic viscosity [η] measured using a mixed solvent of 85% phenol and 15% water at 30°C is 0.05 to 0.15.
Molecular weights corresponding to the range /g are preferred. [η]
If it is less than 0.05, the mechanical strength of the molded article will also decrease, making it difficult to improve the impact resistance according to the present invention. [η]
If it is 0.15 or more, the viscosity of the resin is too high, and the effect of improving drawdown properties by uniform blending with a plasticizer and blending of boric acid or borate is not sufficient. The alcohol-based plasticizer used as a plasticizer in the present invention not only has good compatibility with EVOH and sufficient plasticizing effect, but also facilitates molding and achieves the desired purpose when used in combination with boric acid or borate. This is an important choice in order to obtain the desired effect. In addition, boric acid or boric acid salts are known as gelling agents for polyvinyl alcohol, but by combining them with an alcohol plasticizer in a specific amount and blending them into EVOH in a specific order, it is possible to create a resin composition. For the first time, it becomes possible to produce a resin composition with low drawdown properties, good moldability, sufficient impact resistance, and excellent solvent and oil resistance. Alcohol plasticizers used in the present invention include glycerin, diglycerin, 12-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 2,3-butanediol, 1,4-butanediol, 1,5 pentanediol, 3-methylpentane 1,3,5-triol, 2,5-hexanediol, 1,2,6-hexanetriol, diethanolamine, triethanolamine, diethylene glycol, 2-(2-
Hydroxypropyl) propane 1,3 diol, etc. can be used. The blending ratio of plasticizer is 2~
It is necessary that the content be between 15% by weight, and if it is less than 2 parts by weight, the impact resistance of the resin composition will be insufficient;
If the amount exceeds 15 parts by weight, the effect of improving drawdown properties due to the addition of boric acid or borate cannot be expected, and if the amount exceeds 15 parts by weight, the good compatibility with EVOH will be lost, leading to severe bleeding and stickiness to the molded product. arise. The blending ratio of alcohol plasticizer is 4 to 8.
% by weight is particularly preferred. Compounding agents for improving drawdown properties include:
Boric acid or borates are suitable as they give a uniform gelling effect to the alcoholic plasticizer and EVOH resin. Here, borates refer to hydrated sodium tetraborate, anhydrous sodium tetraborate, and other borates other than sodium. The decrease in drawdown properties is thought to be due to the gelling effect of boric acid or borate. Other gelling agents include organic peroxides, polyvalent isocyanates, polyfunctional epoxy compounds, and polyvalent carboxylic acids, but these cannot simultaneously satisfy drawdown properties and impact resistance, and The surface of the product is likely to become rough. The blending ratio of boric acid or borate needs to be 0.05 to 3 parts by weight. If it is less than 0.05 parts by weight, the drawdown property will be poor and the effect of the present invention will not be recognized, and if it is more than 3 parts by weight, gelation will progress too much or the reaction will not be uniform, resulting in surface roughness and uneven thickness of the molded product. This causes problems such as: From this point of view, the amount of boric acid or boric acid salt added is particularly preferably 0.15 to 1.0 parts by weight. Alcohol plasticizer and boric acid or borate
When blending into EVOH, the order is extremely important. That is, after first sufficiently dissolving boric acid or borate in an alcoholic plasticizer,
Must be mixed (e.g. kneaded) with EVOH.
In other words, contact between the EVOH resin and boric acid or borate without the intervention of an alcohol plasticizer must be avoided. In other words, it is possible to produce a composition with improved impact resistance and good moldability only by following the compounding order of the present invention. Not only does this cause significant variation in the improvement effect, but it also causes uneven thickness of the molded product and roughening of the surface of the molded product. The cause of this is not clear, but prior to the reaction between the hydroxyl group of EVOH and boric acid or borate, the hydroxyl group of the alcohol plasticizer reacts with boric acid or borate, and then the reaction product but
It is believed that the objects of the present invention are achieved by interacting with EVOH resins. This is also inferred from the fact that the object of the present invention is achieved only when an alcohol-based plasticizer is used as a plasticizer through interaction with boric acid or a borate salt. This phenomenon cannot be explained by simple physical effects such as local gelation of boric acid or borate salt and EVOH resin in a system that does not contain an alcoholic plasticizer, resulting in non-uniformity. The specific blending method is to add boric acid or a boric acid salt to an alcohol-based plasticizer heated to 60 to 80℃ and stir to fully dissolve, then add EVOH at a certain ratio to an extruder and knead. The most suitable method is to pelletize it. The multilayer container of the present invention has at least one layer of the composition obtained by the method described above, and is also made of thermoplastic resin such as polyolefin, polyamide, polyester, polyvinyl chloride, or a filler if necessary. It is a blow-molded container having one or more layers of the added composition and, if necessary, an adhesive layer between them. It also includes molded containers processed by deep drawing from sheets and injection molded containers, but the moldability improvement effect of the present invention is particularly suitable for manufacturing blow molded containers. These thermoplastic resin layers are protective layers for the EVOH composition layer,
The material is selected appropriately, taking into consideration the influence of water, strength, moisture permeability, etc. In this case, the processing method usually relies on coextrusion. Also, when molding containers, 1 or 2 shafts can be used.
It is also possible to use an axial stretching method in combination. Applicable
The layer of EVOH composition, i.e. the barrier layer, is
To provide a container that can be in any of the inner layer, middle layer, and outer layer, has little unevenness in thickness, has high impact resistance, so there is no risk of breakage, and there is no risk of loss of content due to permeation of the contents, such as organic drugs, through the wall surface. sell. Antifogging agents, antioxidants, non-alcoholic plasticizers, colorants, fillers, etc. can also be added to the composition used in the present invention, if necessary. The multilayer container of the present invention has excellent inherent chemical resistance,
Not only does it have a barrier function, but it also improves the drop strength, which is a drawback of EVOH resin, and can be manufactured efficiently without uneven thickness, so it can be applied to fields where conventional products were difficult to use. For example, various organic chemicals and agricultural chemicals, sublimation chemicals, petroleum products such as gasoline,
Furthermore, it can be used for edible oils and fats for the purpose of preventing oxidation, hollow bottles for foods such as miso, hard deep-squeezed molded products, etc. In addition, it can also be used for automobile parts that require oil resistance. EXAMPLES Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited by these Examples. The testing and evaluation methods in the experimental examples, working examples, comparative experimental examples, and comparative examples are as follows. Further, the amounts of plasticizer and boric acid or boric acid (boric acid salt) added are expressed as a ratio to the weight of EVOH. 1 MI In accordance with ASTM-D-1238, the resin flow rate for 10 minutes is shown when a load of 2160 kg is applied using a melt indexer. The measurement temperature is 190℃. 2 Izot impact strength Indicates the notched impact strength according to ASTM-D-256. The sample was made by injection molding (thickness and width: 1/2 inch x 1/2 inch) with a 1/10 inch notch, and was left at 20℃ and 65%RH for one week. Measured at 65%RH. 3 Drop test At 20℃, 65%RH, blow container (capacity
Immediately after filling the 500c.c. with 500c.c. of water, the lid is placed on the container, the height is changed, and the container is allowed to fall vertically onto the concrete floor. At each height, the same bottle is dropped up to 10 times and the number of times it does not break is shown. Find the average value using 10 bottles and round it to an integer. 4 Content reduction: Add 500 c.c. of xylene to a blow container (capacity 500 c.c.).
The sample was placed at 50°C for one month and the change in weight was measured. 5. Thickness unevenness of the bottle The thickness unevenness of the bottle body is shown as follows. In the case of a three-layer bottle, the necessary layers were peeled off and the uneven thickness of the bottle body was measured using a dial gauge. Small uneven thickness...Thickness unevenness of 0 to ±10% of the average thickness Medium...Thickness unevenness of ±10 to ±30% of the average thickness Large...Thickness unevenness of ±30 to ±50% of the average thickness Experimental Example 1 When charging EVOH with an ethylene content of 30 mol%, saponification degree of 99.5 mol%, and [η] of 0.10/g to a 40 mmφ extruder, diethylene glycol was added from the hopper port to diethylene glycol at a concentration of 7.5% to diethylene glycol.
Pelletization was carried out while dropping a solution in which % by weight of boric acid had been dissolved in advance to obtain a sample of an EVOH composition containing 8% by weight of diethylene glycol and 0.6% by weight of boric acid. This was used to perform injection molding, samples for Izod impact tests were taken, and impact strength was measured. Next, using this pellet, resin was extruded downward through a pipe having a diameter of 20 mm using a 40 mmφ extruder, and the thickness was measured at 3 cm and 10 cm from the tip of the pipe. The results are shown in Table 1. Comparative Experimental Example 1 Using the EVOH used in Experimental Example 1,
Boric acid and EVOH pellets were dry blended and kneaded into pellets using a 40 mmφ extruder to produce EVOH pellets containing 0.6% by weight of boric acid. Thereafter, diethylene glycol was blended with the boric acid-containing EVOH pellets in the same manner as in Experimental Example 1, and finally EVOH containing 8% by weight of diethylene glycol and 0.6% by weight of boric acid was prepared as in Experimental Example 1.
A sample of the composition was obtained. Regarding this, a test similar to that shown in Experimental Example 1 was conducted. The results are shown in Table 1. Comparative Experimental Example 2 Experimental Example 1 was added to the EVOH used in Experimental Example 1.
Diethylene glycol was blended in the same manner as above.
This blended pellet and boric acid were dry blended and kneaded into pellets in the same manner as in Comparative Experiment Example 1, and finally a sample of the EVOH composition containing 8% by weight of diethylene glycol and 0.6% by weight of boric acid as in Experimental Example 1 was prepared. Obtained. Regarding this, a test similar to that shown in Experimental Example 1 was conducted. The results are shown in Table 1. Comparative Experimental Example 3 A test similar to that shown in Experimental Example 1 was conducted using only the EVOH used in Experimental Example 1. The results are shown in Table 1. Comparative Experimental Example 4 When charging the EVOH used in Experimental Example 1 to a 40 mmφ extruder, a solution of 40% by weight of boric acid dissolved in diethylene glycol was added dropwise to pelletize it, and 8% by weight of diethylene glycol, A sample of an EVOH composition containing 3.2% by weight of boric acid was obtained. Regarding this, a test similar to that shown in Experimental Example 1 was conducted. The results are shown in Table 1. Experimental Example 2 When charging EVOH with an ethylene content of 45 mol%, saponification degree of 99.5 mol%, and [η] of 0.09/g to a 40 mmφ extruder, a water-containing solution of 10% by weight based on the glycerin was added to glycerin from the hopper port. Pelletization is carried out while dropping a solution in which sodium borate has been dissolved in advance, and 10% by weight of glycerin,
Contains 1.0% by weight of hydrated sodium tetraborate
An EVOH composition was obtained. Regarding this, Experimental Example 1
A test similar to that shown was conducted. Table 2 shows the results.
Shown below. Comparative Experimental Example 5 Using the EVOH used in Experimental Example 2,
Sodium tetraborate and EVOH pellets were dry blended and kneaded into pellets using a 40 mmφ extruder to produce EVOH pellets containing 1.0% by weight of sodium tetraborate. Thereafter, glycerin was blended into EVOH pellets containing sodium tetraborate in the same manner as in Experimental Example 1, and finally the same as in Experimental Example 2, 10% by weight of glycerin and 1.0% boric acid.
A sample of the EVOH composition containing % by weight was obtained.
Regarding this, a test similar to that shown in Experimental Example 1 was conducted. The results are shown in Table 2. Comparative Experimental Example 6 Experimental Example 2 was added to the EVOH used in Experimental Example 2.
Glycerin was added in the same manner as above. This blended pellet and sodium tetraborate were dry blended and kneaded into pellets in the same manner as in Comparative Experiment Example 5, and finally an EVOH composition containing 10% by weight of glycerin and 1.0% by weight of boric acid as in Experimental Example 2 was prepared. A sample was obtained. Regarding this, a test similar to that shown in Experimental Example 1 was conducted. The results are shown in Table 2. Comparative Experimental Example 7 A test similar to that shown in Experimental Example 1 was conducted using only the EVOH used in Experimental Example 2. The results are shown in Table 2.

【表】 表1に示すように、上記実験例1によれば同一
の配合割合においても、比較実験例1、2と比較
してよりドローダウン性が良好で、均一配合させ
ることによつて、Izod衝撃強度も高い値となる。
成形物の表面も非常によい光沢を示す。
[Table] As shown in Table 1, according to Experimental Example 1, even at the same blending ratio, the drawdown property was better compared to Comparative Experimental Examples 1 and 2, and by uniformly blending, Izod impact strength also has a high value.
The surface of the molded product also shows very good gloss.

【表】 表2に示すように、上記実験例2によれば同一
の配合割合でも良好な性能を示す。 実施例 1 実験例1で得た試料及びMIが0.8である高密度
ポリエチレン(商品名 三井石油化学製 ハイゼ
ツクス3000B)及び接着性樹脂(商品名 三井石
油化学製 アドマーNF500)の3種類の樹脂を
各々3台の40mmφ押出機を用いて共押出法により
外層が高密度ポリエチレン約800μ、中間層が接
着性樹脂約100μ、内層が実験例1で得られた組
成形物約100μとなるように、内容量500c.c.のブロ
ー成形容器を作成し、ブローボトルの胴部偏肉性
及び落下テスト、内容薬品の重量減少率をしらべ
た。結果を表3に示す。 比較例 1 実施例1で使用した高密度ポリエチレン単独で
壁厚1mm、内容量500c.c.のブロー成形容器を作成
した。各種テスト結果を表3に示す。 比較例 2 実施例1で示した三層ブロー容器の最内層とし
て実験例1で得られたEVOH組成物のかわりに、
比較実験例3で示したEVOHをそのまま未添加
樹脂として使用した内容量500c.c.のブロー成形容
器を作成した。各種テスト結果を表3に示す。 比較例 3 実施例1で示した三層ブロー容器の最内層とし
て、実験例1で得られたEVOH組成物のかわり
に比較実験例1で示したEVOH組成物(ジエチ
レングリコール8重量%、ホウ酸0.6重量%)を
使用した内容量500c.c.のブロー成形容器を作成し
た。各種テスト結果を表3に示す。 比較例 4 実施例1で示した三層ブロー容器の最内層とし
て実験例1で得られたEVOH組成物のかわりに
ナイロン6(東レ製CM1031)を使用した内容量
500c.c.のブロー成形容器を作成した。各種テスト
結果を表3に示す。 実施例 2 実施例1と同様にして共押出法により最外層に
実験例1の試料約100μ、中間層に接着性樹脂約
100μ、最内層に高密度ポリエチレン約800μとな
るよう内容量500c.c.のブロー成形容器を作成した。
実施例1と同様なテストを行つた結果を表3に併
せて示す。このボトルは外観の光沢が非常に秀れ
たものであつた。
[Table] As shown in Table 2, Experimental Example 2 shows good performance even at the same blending ratio. Example 1 The sample obtained in Experimental Example 1 and three types of resins, high-density polyethylene with an MI of 0.8 (product name: Mitsui Petrochemicals Hi-Zex 3000B) and adhesive resin (product name: Mitsui Petrochemicals: Admer NF500), were each used. The contents were co-extruded using three 40mmφ extruders so that the outer layer was about 800μ of high-density polyethylene, the middle layer was about 100μ of adhesive resin, and the inner layer was about 100μ of the composition obtained in Experimental Example 1. A blow-molded container with a capacity of 500 c.c. was made, and the uneven thickness of the body of the blow bottle, a drop test, and the weight reduction rate of the chemical content were investigated. The results are shown in Table 3. Comparative Example 1 A blow-molded container with a wall thickness of 1 mm and an internal capacity of 500 c.c. was prepared using only the high-density polyethylene used in Example 1. Table 3 shows the various test results. Comparative Example 2 Instead of the EVOH composition obtained in Experimental Example 1 as the innermost layer of the three-layer blow container shown in Example 1,
A blow-molded container with an internal capacity of 500 c.c. was prepared using the EVOH shown in Comparative Experiment Example 3 as a non-additive resin. Table 3 shows the various test results. Comparative Example 3 As the innermost layer of the three-layer blow container shown in Example 1, the EVOH composition shown in Comparative Experimental Example 1 (diethylene glycol 8% by weight, boric acid 0.6%) was used instead of the EVOH composition obtained in Experimental Example 1. A blow-molded container with an inner capacity of 500 c.c. Table 3 shows the various test results. Comparative Example 4 Content capacity using nylon 6 (Toray CM1031) instead of the EVOH composition obtained in Experimental Example 1 as the innermost layer of the three-layer blow container shown in Example 1
A blow molded container of 500 c.c. was made. Table 3 shows the various test results. Example 2 In the same manner as in Example 1, approximately 100μ of the sample of Experimental Example 1 was added to the outermost layer and adhesive resin was added to the middle layer using a coextrusion method.
A blow-molded container with an internal capacity of 500 c.c. was made, with a thickness of 100 μm and an innermost layer of high-density polyethylene of approximately 800 μm.
Table 3 also shows the results of a test similar to that of Example 1. This bottle had an extremely glossy appearance.

【表】 * 比較例1は、ポリエチレン層について実
実施2は、最外層について
表3に示すように本発明によれば、ボトル成形
時の問題がなく、落下テストも必要性能を満足し
ている。又キシレンを充填した場合の重量減少率
は、ナイロン及び他の製造法によるよりも非常に
小さい。
[Table] * Comparative Example 1 was carried out on the polyethylene layer.Example 2 was carried out on the outermost layer.As shown in Table 3, according to the present invention, there were no problems during bottle molding, and the drop test also satisfied the required performance. . Also, the weight loss when filled with xylene is much lower than with nylon and other manufacturing methods.

Claims (1)

【特許請求の範囲】[Claims] 1 エチレン含有率25〜60モル%、ケン化度96%
以上のエチレン・ビニルアルコール共重合体樹脂
100重量部、アルコール系可塑剤2〜15重量部及
びホウ酸またはホウ酸塩0.05〜3重量部からな
り、かつホウ酸またはホウ酸塩はアルコール系可
塑剤に溶解された後、エチレン・ビニルアルコー
ル共重合体樹脂と混合せしめられてなる樹脂組成
物の層を少くとも1層含む多層容器。
1 Ethylene content 25-60 mol%, saponification degree 96%
The above ethylene/vinyl alcohol copolymer resins
100 parts by weight, 2 to 15 parts by weight of an alcoholic plasticizer, and 0.05 to 3 parts by weight of boric acid or a boric acid salt, and after the boric acid or boric acid salt is dissolved in the alcoholic plasticizer, ethylene vinyl alcohol is added. A multilayer container comprising at least one layer of a resin composition mixed with a copolymer resin.
JP62212173A 1987-08-25 1987-08-25 Multilayer vessel Granted JPS6372544A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62212173A JPS6372544A (en) 1987-08-25 1987-08-25 Multilayer vessel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62212173A JPS6372544A (en) 1987-08-25 1987-08-25 Multilayer vessel

Publications (2)

Publication Number Publication Date
JPS6372544A JPS6372544A (en) 1988-04-02
JPH0244710B2 true JPH0244710B2 (en) 1990-10-04

Family

ID=16618113

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62212173A Granted JPS6372544A (en) 1987-08-25 1987-08-25 Multilayer vessel

Country Status (1)

Country Link
JP (1) JPS6372544A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0477131A (en) * 1990-07-17 1992-03-11 Kemikaraijingu Kenkyusho:Kk Optical transmitter-receiver

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2673634B1 (en) * 1991-03-08 1994-06-17 Mizoule Henri PLAYING PASTE BASED ON POLYVINYL ALCOHOL.
US6174949B1 (en) 1997-07-25 2001-01-16 Nippon Gohsei Kagaku Kogyo Kabushiki Kaisha Resin composition, process for preparing the same, and laminate containing layer of said resin composition
US8476343B2 (en) 2008-09-16 2013-07-02 Horizon Group Usa Toy putty material compositions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0477131A (en) * 1990-07-17 1992-03-11 Kemikaraijingu Kenkyusho:Kk Optical transmitter-receiver

Also Published As

Publication number Publication date
JPS6372544A (en) 1988-04-02

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