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JP2555081B2 - Styrene resin composition with excellent fluidity and coating adhesion - Google Patents
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JP2555081B2 - Styrene resin composition with excellent fluidity and coating adhesion - Google Patents

Styrene resin composition with excellent fluidity and coating adhesion

Info

Publication number
JP2555081B2
JP2555081B2 JP62150249A JP15024987A JP2555081B2 JP 2555081 B2 JP2555081 B2 JP 2555081B2 JP 62150249 A JP62150249 A JP 62150249A JP 15024987 A JP15024987 A JP 15024987A JP 2555081 B2 JP2555081 B2 JP 2555081B2
Authority
JP
Japan
Prior art keywords
weight
fluidity
parts
coating adhesion
styrene
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
JP62150249A
Other languages
Japanese (ja)
Other versions
JPS63314259A (en
Inventor
恒利 品田
一郎 大塚
晴夫 井上
英夫 市川
久 相原
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP62150249A priority Critical patent/JP2555081B2/en
Publication of JPS63314259A publication Critical patent/JPS63314259A/en
Application granted granted Critical
Publication of JP2555081B2 publication Critical patent/JP2555081B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、流動性に優れ、かつ、成形後の塗装密着性
に優れたスチレン系樹脂組成物に関する。
TECHNICAL FIELD The present invention relates to a styrene resin composition having excellent fluidity and coating adhesion after molding.

〔従来の技術〕[Conventional technology]

スチレン系樹脂は一般に安価で、寸法安定性の良さか
ら多くの成形品に用いられているが、その欠点は一つの
大型成形物、例えば、電子楽器のハウジミング、テレビ
のハウジミング、大型計算機のハウジミング等を成形す
る場合、樹脂の流動性が不足しているための金型の末端
まで樹脂が充填せず、いわゆるショートショツトを起こ
すことである。また、充填できても流動性が悪いと末端
まで圧力が充分にかからず、成形品を金型から抜き出し
たのちにそり、ひけなどの外観不良が生ずることが多
い。
Styrene-based resins are generally used for many molded products because they are inexpensive and have good dimensional stability, but the drawback is one large molded product, such as how to use electronic musical instruments, how to use televisions, how to use large computer, etc. In the case of molding, the resin is not filled up to the end of the mold due to the lack of fluidity of the resin, which causes a so-called short shot. In addition, if the fluidity is poor even if it can be filled, the pressure is not sufficiently applied to the end, and after the molded product is taken out of the mold, a defective appearance such as a warp or a sink mark often occurs.

この問題を解決するため、通常、樹脂の分子量を低下
させたり、流動改良剤として流動パラフィン、エチレン
ビスステアロアミド、高級脂肪酸などの添加が試みられ
ている。これらのうち、前者の分子量低下による流動性
向上は樹脂の衝撃強度を大きく低下させるために通常は
用いられず、後者の添加剤で改良するのが一般的であ
る。
In order to solve this problem, it is usually attempted to reduce the molecular weight of the resin or to add liquid paraffin, ethylene bisstearamide, higher fatty acid or the like as a flow improver. Of these, the former improvement in fluidity due to a decrease in molecular weight is not usually used because it greatly reduces the impact strength of the resin, and the latter additive is generally used for improvement.

これらの流動性改良は成形時、溶融状態の樹脂相互間
で可塑的働きをすると共に、樹脂の表面にブリードする
ことが知られている。
It is known that these fluidity improvements have a plastic function between resins in a molten state at the time of molding and cause bleeding on the surface of the resin.

このため成形物を塗装する場合、表面にブリードした
流動性改良剤の影響で塗装液が弾かれたり、塗膜が容易
に剥離するという問題があり、通常、塗装に先立って塗
装面をアルコールなどでの拭き取りあるいはフッソ系溶
剤による洗浄が行われている。
Therefore, when coating a molded product, there is a problem that the coating liquid is repelled or the coating film is easily peeled off due to the influence of the fluidity improver that bleeds on the surface. It is being wiped off or washed with a fluorine-based solvent.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

したがって、本発明の目的は、塗装前処理の不用なス
チレン系樹脂組成物、具体的には、流動性及び塗装密着
性に優れたスチレン系樹脂組成物を提供することにあ
る。
Therefore, an object of the present invention is to provide a styrene-based resin composition that does not require pretreatment for coating, specifically, a styrene-based resin composition having excellent fluidity and coating adhesion.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者らは、流動性の改良が充分になされ、塗装前
処理を必要とせず、塗装密着性にも優れ、かつ、安価な
添加成分について鋭意探索を行い、この目的を満足する
添加剤を見出し、遂に、本発明に到達した。
The present inventors have made sufficient improvements in fluidity, do not require pretreatment for coating, are excellent in coating adhesion, and have eagerly searched for an inexpensive additive component, and have found an additive satisfying this object. Finally, the present invention has been reached.

すなわち、本発明は、スチレン系樹脂100重量部に対
し、エチレンビスステアロアミドを2.5重量部以下で、
かつヒマシ硬化油とエチレンビスステアロアミドを合計
で0.5〜10重量部含有することを特徴とする流動性及び
塗装密着性に優れたスチレン系樹脂組成物である。
That is, the present invention, with respect to 100 parts by weight of styrene-based resin, ethylene bis stearamide is 2.5 parts by weight or less,
Further, the present invention is a styrene-based resin composition having excellent fluidity and coating adhesion, which contains 0.5-10 parts by weight of castor hardened oil and ethylene bis-stearamide in total.

本発明で使用するスチレン系樹脂とは、スチレンをゴ
ム状エラストマーにグラフト重合した耐衝撃性ポリスチ
レン(HIPS)、アクリロニトリルとスチレンの共重合体
(AS樹脂)、ゴム状エラストマーで補強したAS樹脂(AB
S樹脂)、メチルメタクリレートとスチレンの共重合体
(MS樹脂)、ゴム状エラストマーで補強したAS樹脂(MB
S樹脂)などである。
The styrene-based resin used in the present invention includes impact-resistant polystyrene (HIPS) obtained by graft-polymerizing styrene onto a rubber-like elastomer, a copolymer of acrylonitrile and styrene (AS resin), and AS resin reinforced with a rubber-like elastomer (AB
S resin), copolymer of methyl methacrylate and styrene (MS resin), AS resin reinforced with rubber elastomer (MB
S resin).

本発明で使用するヒマシ硬化油は、ヒマシ油を水素添
加し、融点を84℃以上に高めたものである。
The hydrogenated castor oil used in the present invention is obtained by hydrogenating castor oil to raise its melting point to 84 ° C or higher.

本発明においては、ヒマシ硬化油はエチレンビスステ
アロアミドと併用され、ヒマシ硬化油やエチレンビスス
テアロアミドの単独配合では本発明の効果は得られな
い。すなわち、ヒマシ硬化油の単独配合では流動性及び
塗装密着性は向上するものの耐熱性が大幅に低下する。
また、エチレンビスステアロアミドの単独配合では耐熱
性の低下が少なく、流動性の改良効果が大きいものの塗
料溶剤との相溶性が悪く、特に2.5重量部以上(スチレ
ン系樹脂100重量部に対し)の配合で塗装性が著しく低
下する。したがって、エチレンビスステアロアミドの配
合量はスチレン系樹脂100重量部に対し2.5重量部以下で
あることが必須であり、好ましくは0.05〜2重量部であ
る。
In the present invention, hydrogenated castor oil is used in combination with ethylene bis-stearamide, and the effects of the present invention cannot be obtained by blending castor oil or ethylene bis-stearamide alone. That is, when the castor hardened oil is blended alone, the fluidity and the coating adhesion are improved, but the heat resistance is significantly reduced.
Also, when ethylene bis stearamide is blended alone, there is little decrease in heat resistance and the effect of improving fluidity is great, but the compatibility with paint solvents is poor, especially 2.5 parts by weight or more (based on 100 parts by weight of styrene resin). The blending property markedly reduces the coatability. Therefore, it is essential that the blending amount of ethylenebisstearoamide is 2.5 parts by weight or less, preferably 0.05 to 2 parts by weight, based on 100 parts by weight of the styrene resin.

本発明において、ヒマシ硬化油とエチレンビスステア
ロアミドの合計の配合量は、スチレン系樹脂100重量部
に対し0.5〜10重量部であり、好ましくは1〜5重量部
である。合計の配合量が0.5重量部未満では流動性の改
良効果が充分でなく、10重量部を越えて配合すると成形
時の揮発分が増すという問題があり、かつ、成形物の表
面へのブリードが生じ、従来と同様に塗装前にアルコー
ル拭き取りやフッソ系溶剤洗浄が必要となる。
In the present invention, the total amount of hydrogenated castor oil and ethylene bis-stearamide is 0.5 to 10 parts by weight, preferably 1 to 5 parts by weight, based on 100 parts by weight of the styrene resin. If the total amount is less than 0.5 parts by weight, the effect of improving the fluidity is not sufficient, and if the amount is more than 10 parts by weight, there is a problem that the volatile content at the time of molding increases, and bleeding on the surface of the molded product occurs. As is the case with the conventional method, alcohol wiping or fluorine solvent cleaning is required before painting.

本発明のスチレン系樹脂組成物は、スチレン系樹脂に
ヒマシ硬化油とエチレンビスステアロアミドを、ヘンシ
ェルミキサー、混練ロール、バンバリーミキサーなどで
混合したのち、押し出し機で押し出すことにより、ま
た、スチレン系樹脂を製造する重合系にこれら成分を添
加しておくとこにより製造できる。
The styrene-based resin composition of the present invention is a styrene-based resin, castor hydrogenated oil and ethylene bis-stearamide are mixed with a Henschel mixer, a kneading roll, a Banbury mixer, and the like. It can be produced by adding these components to a polymerization system for producing a resin.

本発明の組成物は、さらに酸化防止剤、着色剤や界面
活性剤などの各種添加剤を含有していてもかまわない。
The composition of the present invention may further contain various additives such as an antioxidant, a colorant and a surfactant.

〔実施例〕〔Example〕

以下、実施例により本発明を説明する。 Hereinafter, the present invention will be described with reference to examples.

実施例1〜2 ゴム状エラストマー10重量部の存在下にスチレン75重
量部とアクリロニトリル25重量部の混合物を重合して得
たABS樹脂(三井東圧化学(株)製:商品名 サンタッ
クGT−10)100重量部に、ヒマシ硬化油とエチレンビス
ステアロアミドを表−1に示す量を混合し、押し出し機
にてペレット化した。
Examples 1 and 2 ABS resin obtained by polymerizing a mixture of 75 parts by weight of styrene and 25 parts by weight of acrylonitrile in the presence of 10 parts by weight of rubber-like elastomer (manufactured by Mitsui Toatsu Chemicals, Inc .: trade name Santak GT-10). ) 100 parts by weight of hydrogenated castor oil and ethylene bisstearamide were mixed in the amounts shown in Table 1 and pelletized by an extruder.

得られた樹脂組成物の流動性(メルトフロー値)をJI
S K−6871に従って測定した。
Determine the fluidity (melt flow value) of the obtained resin composition by JI
It was measured according to SK-6871.

塗装密着性は50×50×2.5mmの平板成形物を射出成形
し、通常のプラスチック用塗料であるウレタン系塗料
(長嶋塗料(株)製:商品名 X−361)及びアクリル
系塗料(東邦化研(株)製:商品名 ポリタック)を塗
装し、JIS K−5400に従い碁盤目試験により測定した。
Paint adhesion is 50 x 50 x 2.5 mm flat plate molded product by injection molding, and urethane paint (Nagashima Paint Co., Ltd .: trade name X-361) and acrylic paint (Toho Kaika) Kenken Co., Ltd .: trade name Polytac) was applied and measured by a cross-cut test according to JIS K-5400.

また、耐熱性はJIS K−6870に従ってビカット軟化点
により測定した。
The heat resistance was measured by the Vicat softening point according to JIS K-6870.

得られた結果を表−1に示す。 The obtained results are shown in Table-1.

比較例1〜5 ヒマシ硬化油およびエチレンビスステアロアミドの配
合量を表−1に示す量とする他は実施例1〜2と同様に
した。結果を表−1に示す。
Comparative Examples 1 to 5 The same as Examples 1 to 2 except that the amounts of hydrogenated castor oil and ethylene bisstearamide were changed to the amounts shown in Table 1. The results are shown in Table 1.

実施例3〜4 ゴム状エラストマー7.5重量%にスチレン92.5重量%
をグラフト重合して得たHIPS(三井東圧化学(株)製:
商品名 トーポレックス860−03)100重量部に表−1に
示す量ヒマシ硬化油及びエチレンビスステアロアミドを
配合する他の実施例1〜2と同様にした。結果を表−1
に示す。
Examples 3 to 4 Rubber-like elastomer 7.5% by weight and styrene 92.5% by weight
HIPS obtained by graft polymerization of (manufactured by Mitsui Toatsu Chemicals, Inc .:
Trade name Topolex 860-03) 100 parts by weight of castor hydrogenated oil and ethylene bis stearamide shown in Table 1 were blended in the same manner as in other Examples 1 and 2. The results are shown in Table-1
Shown in

比較例6〜7 ヒマシ硬化油及びエチレンビスステアロアミドに代え
て表−1に示す化合物を表−1に示す量用いる他は実施
例3〜4と同様にした。結果を表−1に示す。
Comparative Examples 6 to 7 Comparative Examples 6 to 7 were performed in the same manner as in Examples 3 to 4, except that the compounds shown in Table 1 were used in the amounts shown in Table 1 in place of hydrogenated castor oil and ethylenebisstearoamide. The results are shown in Table 1.

〔発明の効果〕 ヒマシ効果油単独使用では流動性が改良されるが、塗
装密着性が不足し(比較例1)、エチレンビスステアロ
アミドの単独使用では耐熱性を維持しつつ流動性が改良
されるが塗装密着性が大幅に低下している(比較例
2)。また、合計の使用量が少なすぎると流動性が不足
し(比較例3)、多すぎると流動性が改良されているも
のの塗装密着性および耐熱性が低下する(比較例4)。
さらに合計の使用量が本発明の範囲内であってもエチレ
ンビスステアロアミドの配合量が多すぎると塗装密着性
が低下する(比較例5)。
EFFECTS OF THE INVENTION Castor effect oil alone improves fluidity, but coating adhesion is insufficient (Comparative Example 1), and ethylenebisstearoamide alone improves fluidity while maintaining heat resistance. However, the coating adhesion is significantly reduced (Comparative Example 2). Further, if the total amount used is too small, the fluidity is insufficient (Comparative Example 3), and if the total amount is too large, the fluidity is improved but the coating adhesion and heat resistance are reduced (Comparative Example 4).
Further, even if the total amount used is within the range of the present invention, if the blending amount of ethylenebisstearoamide is too large, the coating adhesion will be reduced (Comparative Example 5).

なお、高級脂肪酸の単独配合では流動性が改良される
ものの耐熱性および塗装密着性は低下しており(比較例
6)、金属石鹸の単独配合では流動性が改良され、耐熱
性も充分であるが塗装密着性が低下する(比較例7)。
It should be noted that the blending of the higher fatty acid alone improves the fluidity, but the heat resistance and the coating adhesion are lowered (Comparative Example 6), and the blending of the metal soap alone improves the fluidity and has sufficient heat resistance. However, the coating adhesion decreases (Comparative Example 7).

本発明の組成物は実施例に見られるように、流動性、
塗装密着性および耐熱性のいずれもがバランスよく優れ
ており、大型の成形物、例えば、テレビのハウジング、
電子楽器のハウジング、エアコンのハウジングなどが容
易に成形でき、かつ、前処理をすることなく塗装できる
という極めて優れた性質を有しており、その産業上に寄
与すること大である。
The composition of the present invention, as seen in the examples, has a fluidity,
Both coating adhesion and heat resistance are excellent in a well-balanced manner, and large moldings, such as TV housings,
The housing of an electronic musical instrument, the housing of an air conditioner, etc. can be easily molded and can be painted without pretreatment, which is an extremely excellent property, which greatly contributes to the industry.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】スチレン系樹脂100重量部に対し、エチレ
ンビスステアロアミド0.05〜2.5重量部及びヒマシ硬化
油0.45〜9.95重量部を含有し、かつヒマシ硬化油とエチ
レンビスステアロアミドを合計で0.5〜10重量部含有す
ることを特徴とする流動性及び塗装密着性に優れたスチ
レン系樹脂組成物。
1. A styrene resin containing 0.05 to 2.5 parts by weight of ethylene bis-stearamide and 0.45 to 9.95 parts by weight of castor-hardened oil, and hydrogenated castor oil and ethylene bis-stearamide in total. A styrene-based resin composition excellent in fluidity and coating adhesion, characterized by containing 0.5 to 10 parts by weight.
JP62150249A 1987-06-18 1987-06-18 Styrene resin composition with excellent fluidity and coating adhesion Expired - Lifetime JP2555081B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62150249A JP2555081B2 (en) 1987-06-18 1987-06-18 Styrene resin composition with excellent fluidity and coating adhesion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62150249A JP2555081B2 (en) 1987-06-18 1987-06-18 Styrene resin composition with excellent fluidity and coating adhesion

Publications (2)

Publication Number Publication Date
JPS63314259A JPS63314259A (en) 1988-12-22
JP2555081B2 true JP2555081B2 (en) 1996-11-20

Family

ID=15492818

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62150249A Expired - Lifetime JP2555081B2 (en) 1987-06-18 1987-06-18 Styrene resin composition with excellent fluidity and coating adhesion

Country Status (1)

Country Link
JP (1) JP2555081B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2758031B2 (en) * 1989-07-04 1998-05-25 協和化学工業株式会社 Stabilizer composition for halogen-containing resin
JP7708731B2 (en) * 2021-10-08 2025-07-15 Psジャパン株式会社 Styrenic resin composition and molded article thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5491556A (en) * 1977-12-29 1979-07-20 Toray Ind Inc Thermoplastic resin composition

Also Published As

Publication number Publication date
JPS63314259A (en) 1988-12-22

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