JP6896025B2 - 熱可塑性樹脂組成物、成形品および製品 - Google Patents
熱可塑性樹脂組成物、成形品および製品 Download PDFInfo
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- JP6896025B2 JP6896025B2 JP2019128443A JP2019128443A JP6896025B2 JP 6896025 B2 JP6896025 B2 JP 6896025B2 JP 2019128443 A JP2019128443 A JP 2019128443A JP 2019128443 A JP2019128443 A JP 2019128443A JP 6896025 B2 JP6896025 B2 JP 6896025B2
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Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/02—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
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Description
ポリオキシエチレン鎖を有する親水性コポリマー(B)と、
下記式(1)で表される脂肪酸金属塩(C)と、を含有する、熱可塑性樹脂組成物。
M(OH)y(R−COO)x ・・・(1)
(式(1)中、Rは、炭素数6〜40のアルキル基またはアルケニル基である。Mは、アルミニウム、亜鉛、カルシウム、マグネシウム、リチウムおよびバリウムからなる群から選択される少なくとも1種の金属元素である。xおよびyはそれぞれ独立な0以上の整数であり、x+y=[Mの価数]の関係を満たす。)
本実施の形態の熱可塑性樹脂組成物は、
スチレン系樹脂(A)と、
ポリオキシエチレン鎖を有する親水性コポリマー(B)と、
脂肪酸金属塩(C)と、を含有する。
オレフィン系樹脂(A)は、ラジカル重合性二重結合を有するオレフィン系単量体を重合又は共重合させてなる合成樹脂である。
親水性コポリマー(B)は、ポリオキシエチレン鎖を有する。ポリオキシエチレン鎖は親水性セグメントとして機能するため、ポリオキシエチレン鎖を有することで、帯電防止性能を発現し、親水性の粉塵汚れの付着を抑制する効果を発現する。
脂肪酸金属塩(C)は、下記式(1)で表される化合物である。
M(OH)y(R−COO)x ・・・(1)
(式(1)中、Rは、炭素数6〜40のアルキル基またはアルケニル基である。Mは、アルミニウム、亜鉛、カルシウム、マグネシウム、リチウムおよびバリウムからなる群から選択される少なくとも1種の金属元素である。xおよびyはそれぞれ独立な0以上の整数であり、x+y=[Mの価数]の関係を満たす。)
M(OH)y(R−COO)x ・・・(1)
(式(1)中、Rは、炭素数6〜40のアルキル基またはアルケニル基である。Mは、アルミニウム、亜鉛、カルシウム、マグネシウム、リチウムおよびバリウムからなる群から選択される少なくとも1種の金属元素である。xおよびyはそれぞれ独立な0以上の整数であり、x+y=[Mの価数]の関係を満たす。)
式(1)において、Mは、アルミニウム、亜鉛、カルシウム、マグネシウム、リチウムおよびバリウムからなる群から選択される少なくとも1種の金属元素である。
本実施の形態の脂肪酸金属塩(C)を構成する脂肪酸としては、例えば、カプロン酸、カプリン酸、ラウリン酸、パルミチン酸、ステアリン酸、ベヘン酸、リグノセリン酸、モンタン酸、オレイン酸、リノール酸等が挙げられる。脂肪酸は、ステアリン酸、ベヘン酸、モンタン酸などの長鎖脂肪酸(炭素数12以上の脂肪酸)であることが好ましい。特に、ステアリン酸は、入手し易く安価なため製造にはより好ましい。
式(1)において、xおよびyはそれぞれ独立な0以上の整数であり、x+y=[Mの価数]の関係を満たす。
本実施の形態の熱可塑性樹脂組成物において、親水性コポリマー(B)の配合量は、オレフィン系樹脂(A)100質量部に対して、好ましくは1〜20質量部であり、更に好ましくは1〜17質量部である。
本実施の形態の熱可塑性樹脂組成物は、本実施の形態の目的を損なわない範囲で、任意成分として、例えば、熱安定剤、紫外線吸収剤、光安定剤、抗菌剤、防黴剤、無機充填材などの成分を含んでいてもよい。
本実施の形態の熱可塑性樹脂組成物は、製造時等の熱安定性を向上するために、熱安定剤を含んでいてもよい。
上記ラクトン系安定剤、ホスファイト化合物、およびヒンダードフェノール化合物を混合した安定剤として、Irganox HP−2921(登録商標、CIBA SPECIALTY CHEMICALS社製)等が市販されている。
本実施の形態の熱可塑性樹脂組成物は、紫外線吸収剤を含有してもよい。本実施の形態の熱可塑性樹脂組成物は、ゴム成分等の影響によって耐候性に劣る場合があることから、耐候性を向上するために紫外線吸収剤の配合は有効である。
本実施の形態の熱可塑性樹脂組成物は、光安定剤を含有してもよい。本実施の形態の熱可塑性樹脂組成物は、暗所黄変を起こす場合があることから、かかる劣化を防止するため光安定剤の配合は有効である。
本実施の形態の熱可塑性樹脂組成物は、抗菌剤を含んでいてもよい。抗菌剤としては、特に限定されるものではないが、例えば、酸化亜鉛、銀、銅、亜鉛等の抗菌性金属を、結晶性アルミノケイ酸塩、無定形アルミノケイ酸塩、シリカゲル、活性アルミナ、けいそう土、活性炭、リン酸ジルコニウム、ヒドロキシアパタイト、酸化マグネシウム、過塩素酸マグネシウム、ガラス等に担持してなる無機系抗菌剤が挙げられる。抗菌性金属としては、酸化亜鉛が好ましい。
本実施の形態の熱可塑性樹脂組成物は、剛性を付与し強度を向上する目的で強化フィライーとして、無機充填剤を含んでいてもよい。
本実施の形態で使用可能な他の任意成分としては、着色の為の染料、顔料、消泡剤、可塑剤、滑剤、離型剤および難燃剤等を挙げることができる。更には、オレフィン系樹脂(A)および親水性コポリマー(B)以外の熱可塑性樹脂を本実施の形態の目的を損なわない範囲で配合することも可能である。
オレフィン系樹脂である、ポリオレフィン系樹脂(高密度ポリエチレン 、低密度ポリエチレン、ポリプロピレン等)、環状オレフィン系樹脂、および、ポリエステル系樹脂(ポリ乳酸、ポリエチレンテレフタレート、ポリブチレンテレフタレート等)、
スチレン系樹脂である、ポリスチレン(PS樹脂)、アクリロニトリルブタジエンスチレン(ABS樹脂)、および、アクリロニトリルスチレン(AS樹脂)、
ABS樹脂のブタジエンに代替しアクリルゴムを重合させたASA樹脂、
ABS樹脂のブタジエンに代替しエチレン系ゴムを重合させたAES樹脂、
メチルメタクリレートブタジエンスチレン(MBS樹脂)などが挙げられる。
本実施の形態の熱可塑性樹脂組成物の製造には、任意の方法が採用される。例えばオレフィン系樹脂(A)、親水性コポリマー(B)、脂肪酸金属塩(C)および任意に他の添加剤を、V型ブレンダー、ヘンシェルミキサー、メカノケミカル装置、押出混合機などの予備混合手段を用いて充分に混合した後、必要に応じて押出造粒器やブリケッティングマシーンなどによりかかる予備混合物の造粒を行い、その後ベント式二軸押出機に代表される溶融混練機で溶融混練し、その後ペレタイザーによりペレット化する方法が挙げられる。
本実施の形態に係る成形品は、上記の熱可塑性樹脂組成物からなる。本実施の形態に係る成形品では、上記の熱可塑性樹脂組成物からなることにより、親水性の粉塵汚れと疎水性の粉塵汚れとの両方の付着を抑制する効果が奏される。
本実施の形態の製品は、上記の成形品を備える。すなわち、上記の成形品は、例えば、家電製品、OA機器等の製品の樹脂製部品(内部部品、ハウジング等)として用いられる。本実施の形態の製品では、上記の成形品を備えることにより、清潔性の向上とメンテナンス頻度の削減の効果が奏される。
(1)引張り強度
ISO 527−1,2に従い、引張り強度(引張り降伏強度)の測定を実施した。測定値を使用したオレフィン系樹脂(A成分)単体の引張り強度と比較し、下記の基準に基づいて評価した。
A:保持率が95%以上、B:保持率が95%未満、90%以上、C:保持率が90%未満、85%以上、D:85%未満
ISO 178に従い、曲げ弾性率を測定した(試験片寸法:長さ80mm×幅10mm×厚み4mm)。測定値を使用したオレフィン系樹脂(A成分)の曲げ弾性率と比較し、下記の基準に基づいて評価した。
A:保持率が95%以上、B:保持率が95%未満、90%以上、C:保持率が90%未満、85%以上、D:85%未満
ISO 179に従い、ノッチ付きのシャルピー衝撃強度の測定を実施した。
150mm×150mm×2mm(厚み)の角板を、射出成型機を用いて成形し、高速面衝撃試験をN=5で実施し、面衝撃強度(破壊エネルギー)を測定し、N=5の平均値を求めた。また、破壊形態について、下記の基準に基づいて評価した。
A:延性的な破壊、B:延性的な破壊と脆性的破壊の混在(延性的は破壊数>脆性的破壊数)、C:延性的な破壊と脆性的破壊の混在(脆性的は破壊数>延性的な破壊数)、D:脆性的な破壊
ISO 75−1および75−2に従い、荷重たわみ温度を測定した。なお、測定荷重は1.80MPaで実施した。
150mm×150mm×2mm(厚み)の角板を作成し、23℃、湿度50%の環境にて一週間放置した後、該角板について粉塵付着性の試験を実施した。親水性の粉塵付着性評価には、関東ローム(JIS試験用紛体11種)を使用し、疎水性の粉塵付着性評価には、カーボンブラック(JIS試験用紛体12種)を使用した。
粉塵付着性の評価は、粉塵をエアーで成形品表面に一定量(5g)吹きつけた後の、成形品表面をKEYENCE製デジタルマイクロスコープVHX−5000により100倍で観察し、画像処理により粉塵付着面積割合を求めて、下記の基準に基づいて評価した。
A:粉塵付着面積割合が3%未満、B:粉塵付着面積割合が3〜6%未満、C:粉塵付着面積割合が6〜9%未満、D:粉塵付着面積割合が9%以上
表1〜表4に示すA〜C成分100質量部(A〜C成分の総量)、離型剤[理研ビタミン(株)製:リケスター EW400(製品名)]0.3質量部、リン系熱安定剤 [BASF製 IRGAFOS168(製品名)]0.1質量部、フェノール系熱安定剤 [BASF製;IRGANOX1076(製品名)]0.1質量部、ヒンダードアミン系光安定剤 [(株)ADEKA製 アデカスタブ LA−57(製品名)]0.2質量部、および、ベンドトリアゾール系紫外線吸収剤 [シプロ化成(株)製 SEESORB701(製品名)]0.1質量部をV型ブレンダーで混合し、混合物を得た。
(PP1)
ポリプロピレン(ホモポリマー)[プライムポリマー社製、J137M、結晶核剤を約0.1%の割合で含むホモポリプロピレン、MFR=30g/10分(230℃/2.16kgf)]
(PP2)
ポリプロピレン(ブロックコポリマー)[プライムポリマー社製、J830HV、共重合の形態がブロックコポ リマー、MFR=30g /10分(230℃/2.16kgf)]
(PEPO−1)
ポリオレフィンのブロックと親水性ポリマーのブロックが繰り返し交互に結合した構造を有するコポリマー [三洋化成工業製、ぺレクトロン HS (商品名)、表面抵抗値=4×105Ω]
(PEPO−2)
ポリエーテルエステルアミド [三洋化成工業製、ペレスタットNC6321(商品名)、表面抵抗値=1×109Ω]
(StZn)
ステアリン酸亜鉛[日油株式会社製、ジンクステアレート(製品名)、金属含有量=10.5〜11.3%、遊離脂肪酸=0.5%以下]
(StAl−1)
モノステアリン酸(ジヒドロキシ)アルミニウム[日油株式会社製、アルミニウムステアレート300(製品名)、金属含有量=10.0〜11.5%、遊離脂肪酸=8.0%以下]
(StAl−2)
ジステアリン酸(ヒドロキシ)アルミニウム[日油株式会社製、アルミニウムステアレート600(製品名)、金属含有量=8.5〜10.0%、遊離脂肪酸=12.0%以下]
(StAl−3)
トリステアリン酸アルミニウム[日油株式会社製、アルミニウムステアレート900(製品名)、金属含有量=6.5〜8.0%、遊離脂肪酸=20〜30%]
Claims (7)
- オレフィン系樹脂(A)と、
ポリオキシエチレン鎖を有する親水性コポリマー(B)と、
下記式(1)で表される脂肪酸金属塩(C)と、を含有する、熱可塑性樹脂組成物。
M(OH)y(R−COO)x ・・・(1)
(式(1)中、Rは、炭素数6〜40のアルキル基またはアルケニル基である。Mは、アルミニウムである。xは1以上の整数であり、yは0以上の整数であり、x+y=[Mの価数]の関係を満たす。) - 前記オレフィン系樹脂(A)100質量部と、前記親水性コポリマー(B)1〜20質量部と、前記脂肪酸金属塩(C)0.6〜10質量部と、を含有する、請求項1に記載の熱可塑性樹脂組成物。
- 前記親水性コポリマー(B)が、ポリオレフィンとポリオキシエチレン鎖を有する親水性ポリマーとが繰り返し交互に結合してなる親水性コポリマー(B1)である、請求項1または2に記載の熱可塑性樹脂組成物。
- 前記親水性コポリマー(B)の表面抵抗値が1×104〜1×107Ωである、請求項1〜3のいずれか1項に記載の熱可塑性樹脂組成物。
- 前記式(1)において、y=1である、請求項1〜4のいずれか1項に記載の熱可塑性樹脂組成物。
- 請求項1〜5のいずれか1項に記載の熱可塑性樹脂組成物からなる成形品。
- 請求項6に記載の成形品を備える製品。
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