JPH05320487A - Thermoplastic resin composition - Google Patents

Thermoplastic resin composition

Info

Publication number
JPH05320487A
JPH05320487A JP13116092A JP13116092A JPH05320487A JP H05320487 A JPH05320487 A JP H05320487A JP 13116092 A JP13116092 A JP 13116092A JP 13116092 A JP13116092 A JP 13116092A JP H05320487 A JPH05320487 A JP H05320487A
Authority
JP
Japan
Prior art keywords
resin
resin composition
group
weight
polystyrene resin
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.)
Pending
Application number
JP13116092A
Other languages
Japanese (ja)
Inventor
Eizou Touzaki
栄造 東崎
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite 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 Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP13116092A priority Critical patent/JPH05320487A/en
Publication of JPH05320487A publication Critical patent/JPH05320487A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a thermoplastic resin composition markedly improved in the compatibility of the constituent polyester resin with the constituent polystyrene resin, excellent in moldability and being capable of giving a material excellent in mechanical strengths and heat and chemical resistance. CONSTITUTION:This resin composition is prepared by adding 0.1-20 pts.wt. modified polystyrene resin containing at least one functional group selected from among an acid anhydride group, an epoxy group and an oxazoline group to 100 pts.wt. resin composition comprising 95-5wt.% polyester resin and 5-95wt.% polystyrene resin.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、ポリエステル系樹脂及
びポリスチレン系樹脂を主成分とし、ポリエステル系樹
脂の末端である水酸基或いはカルボン酸基と反応する基
を含有する変性ポリスチレン系樹脂を所定量添加するこ
とにより双方の相溶性の改善が図られ、良好な耐熱性、
耐衝撃性、成形加工性及び耐薬品性を有することを特徴
とするフィルムシート、或いはコンパウンドに用いられ
る熱可塑性樹脂組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention comprises a polyester-based resin and a polystyrene-based resin as main components, and adds a predetermined amount of a modified polystyrene-based resin containing a group reactive with a hydroxyl group or a carboxylic acid group at the end of the polyester-based resin. By doing so, the compatibility of both can be improved, and good heat resistance,
The present invention relates to a thermoplastic resin composition used for a film sheet or a compound, which has impact resistance, moldability and chemical resistance.

【0002】[0002]

【従来の技術】飽和ポリエステル系樹脂は、その構造に
より多少の変わりはあるが、一般に表面平滑性に富み、
光沢のある外観を有している。結晶性のPET,PBT
は、高い融点、高い結晶化度を有しており、寸法安定
性、透明性、強靭性、電気絶縁性、耐薬品性に優れフィ
ルムシート、成形品などに広く用いられているが、成形
加工性が悪いという欠点を有している。一方、非晶性の
PC,PARは、耐熱性、機械特性、透明性に優れ、耐
衝撃性についても結晶性のPET,PBTに較べかなり
良好であり、電気電子部品、OA機器、精密機械等の用
途に用いられているが、耐溶剤性が悪いという欠点を有
している。一方、PS,AS等のポリスチレン系樹脂
は、成形性、コスト、透明性に極めて優れ、又軽量であ
るため、日用雑貨、プラモデル等広範囲の用途に用いら
れているが、耐衝撃性、耐溶剤性が悪いという欠点を有
している。一般に耐熱性、耐衝撃性、成形性、耐薬品性
等の諸特性がいずれも良好な樹脂組成物は単一の樹脂か
ら得ることは困難であるため、各々の欠点を補うことが
可能な二種以上の樹脂を組み合わせるポリマーアロイと
いう手法が用いられる。しかしながら、通常各樹脂間の
相溶性は悪く、単に混ぜ合わせただけでは非相溶ミクロ
相分離構造をとることが出来ないため各樹脂の長所を合
わせ持つような熱可塑性樹脂を得ることは困難であっ
た。相溶性の改善を図る方法としては、組み合わせる樹
脂のいずれにも親和性を有する相溶化剤を添加する方法
が一般に行われるが、ポリエステル系樹脂とポリスチレ
ン系樹脂の場合は好適な相溶化剤は無く改善効果が不十
分であった。
2. Description of the Related Art Saturated polyester resins are generally rich in surface smoothness, although they may vary depending on their structure.
It has a glossy appearance. Crystalline PET, PBT
Has a high melting point and high crystallinity, and is widely used for film sheets, molded products, etc., with excellent dimensional stability, transparency, toughness, electrical insulation, and chemical resistance. It has the disadvantage of poor performance. On the other hand, amorphous PC and PAR are excellent in heat resistance, mechanical properties and transparency, and have much better impact resistance than crystalline PET and PBT. However, it has the drawback of poor solvent resistance. On the other hand, polystyrene resins such as PS and AS have excellent moldability, cost and transparency, and are lightweight, so they are used in a wide range of applications such as daily sundries and plastic models. It has the drawback of poor solvent properties. Generally, it is difficult to obtain a resin composition having good properties such as heat resistance, impact resistance, moldability, chemical resistance, etc. from a single resin. A technique called polymer alloy is used in which two or more kinds of resins are combined. However, the compatibility between each resin is usually poor, and it is difficult to obtain a thermoplastic resin having the advantages of each resin because it is not possible to form an incompatible micro phase separation structure simply by mixing them. there were. As a method for improving the compatibility, a method of adding a compatibilizing agent having an affinity to any of the resins to be combined is generally performed, but in the case of polyester resin and polystyrene resin, there is no suitable compatibilizing agent. The improvement effect was insufficient.

【0003】[0003]

【発明が解決しようとする課題】本発明ではポリエステ
ル系樹脂、ポリスチレン系樹脂のいずれにも親和性を有
する相溶化剤を得るべく鋭意検討した結果、ポリエステ
ル系樹脂の末端である水酸基或いはカルボン酸基の反応
に活性を持つ酸無水物、エポキシ基及びオキサゾリン基
のうち少なくとも1種の官能基を含有する変性ポリスチ
レン系樹脂が、ポリエステル系樹脂とポリスチレン系樹
脂との相溶性を著しく改善し、成形加工性、機械的強
度、耐熱性及び耐薬品性に優れた材料が得られることを
見いだし、本発明を完成するに至った。
DISCLOSURE OF THE INVENTION In the present invention, as a result of extensive studies to obtain a compatibilizer having an affinity for both polyester resins and polystyrene resins, it was found that the terminal hydroxyl group or carboxylic acid group of the polyester resin is A modified polystyrene resin containing at least one functional group of an acid anhydride, an epoxy group and an oxazoline group, which is active in the reaction of, significantly improves the compatibility between the polyester resin and the polystyrene resin, and the molding process is performed. It was found that a material having excellent properties, mechanical strength, heat resistance and chemical resistance can be obtained, and the present invention has been completed.

【0004】[0004]

【課題を解決するための手段】即ち本発明は、ポリエス
テル系樹脂95〜5重量%及びポリスチレン系樹脂5〜
95重量%から成る樹脂組成物100重量部に対して、
酸無水物基、エポキシ基及びオキサゾリン基のうち少な
くとも1種の官能基を含有する変性ポリスチレン系樹脂
を0.1〜20重量部添加することを特徴とする熱可塑
性樹脂組成物に関するものである。
That is, according to the present invention, 95 to 5% by weight of a polyester resin and 5 to 5 of a polystyrene resin are used.
With respect to 100 parts by weight of the resin composition consisting of 95% by weight,
It relates to a thermoplastic resin composition comprising 0.1 to 20 parts by weight of a modified polystyrene resin containing at least one functional group selected from an acid anhydride group, an epoxy group and an oxazoline group.

【0005】本発明の熱可塑性樹脂で用いられるポリエ
ステル系樹脂は特に限定するものではなく市販されてい
るものであり、例えば、ポリエチレンテレフタレート
(PET),ポリブチレンテレフタレート(PBT),
芳香族ポリカーボネート、ポリアリレート、液晶ポリエ
ステル及び複数の原料成分を用いることにより得られる
共重合ポリエステル樹脂が挙げられる。これらは、単独
或いは二種以上組み合わせて用いられる。
The polyester resin used in the thermoplastic resin of the present invention is not particularly limited and is commercially available. For example, polyethylene terephthalate (PET), polybutylene terephthalate (PBT),
Examples thereof include aromatic polycarbonate, polyarylate, liquid crystal polyester, and copolyester resin obtained by using a plurality of raw material components. These may be used alone or in combination of two or more.

【0006】本発明の熱可塑性樹脂組成物で用いられる
ポリスチレン系樹脂は特に限定するものではなく市販さ
れているものであり、例えば、ポリスチレン、アクリロ
ニトリル−スチレン共重合体等が挙げられる。これらの
樹脂は、単独或いは二種以上組み合わせて用いられる。
The polystyrene resin used in the thermoplastic resin composition of the present invention is not particularly limited and is commercially available, and examples thereof include polystyrene and acrylonitrile-styrene copolymer. These resins may be used alone or in combination of two or more.

【0007】本発明において、ポリエステル系樹脂
(A)とポリスチレン系樹脂(B)は、(A):(B)
=95:5〜5:95重量部、好ましくは90:10〜
10:90重量部の範囲で配合される。ポリスチレン系
樹脂の配合量が5重量部を下回ると、成形加工性の改善
が不十分となり、又ポリエステル系樹脂の配合量が5重
量部を下回ると、耐熱性、耐溶剤性の改善効果が不十分
となる。
In the present invention, the polyester resin (A) and the polystyrene resin (B) are (A) :( B)
= 95: 5-5: 95 parts by weight, preferably 90:10
It is compounded in the range of 10:90 parts by weight. If the amount of the polystyrene resin compounded is less than 5 parts by weight, the molding processability is insufficiently improved. If the amount of the polyester resin compounded is less than 5 parts by weight, the heat resistance and solvent resistance are not improved. Will be enough.

【0008】本発明の変性ポリスチレン系樹脂は、ポリ
エステル系樹脂の末端である水酸基或いはカルボン酸基
の反応に活性を持つ酸無水物基、エポキシ基及びオキサ
ゾリン基のうち少なくとも1種の官能基を有するスチレ
ン系共重合体であり、これら変性ポリスチレン系樹脂の
合成法としては、公知のラジカル重合法が適用でき、溶
液或いは懸濁重合などにより容易に得ることができる。
また、本発明の変性ポリスチレン系樹脂の変性率(重合
仕込時における官能基含有モノマーの重量比)は、0.
1〜20wt%であり、好ましくは1〜18wt%であ
る。変性率が0.1wt%を下回ると、相溶性の改善効
果が得られず、また、変性率が20wt%を上回ると、
ポリエステル系樹脂との反応による高分子量化により成
形性などの諸特性が低下する。これら変性ポリスチレン
系樹脂は単独或いは二種以上組み合わせて用いられる。
The modified polystyrene resin of the present invention has at least one functional group selected from the group consisting of an acid anhydride group, an epoxy group and an oxazoline group, which is active in the reaction of the terminal hydroxyl group or carboxylic acid group of the polyester resin. A known radical polymerization method can be applied as a method for synthesizing the modified polystyrene resin, which is a styrene copolymer, and can be easily obtained by solution or suspension polymerization.
The modified polystyrene resin of the present invention has a modification ratio (weight ratio of the functional group-containing monomer at the time of polymerization) of 0.
It is 1 to 20 wt%, preferably 1 to 18 wt%. If the modification rate is less than 0.1 wt%, the effect of improving compatibility cannot be obtained, and if the modification rate exceeds 20 wt%,
Various properties such as moldability deteriorate due to the increase in the molecular weight due to the reaction with the polyester resin. These modified polystyrene resins may be used alone or in combination of two or more.

【0009】ポリエステル系樹脂とポリスチレン系樹脂
とを所定の割合で配合した樹脂組成物100重量部に対
し、変性ポリスチレン系樹脂を0.1〜20重量部配合
し、二軸混練機などで混練する事により相溶性が良好な
熱可塑性樹脂組成物を得ることができる。変性ポリスチ
レン系樹脂の配合量が0.1重量部を下回ると、相溶性
の改善効果が不十分となり、又、配合量が20重量部を
上回ると、相溶性が良くなり過ぎ特性が低下する。この
ように本発明の変性ポリスチレン系樹脂は、ポリエステ
ル系樹脂とポリスチレン系樹脂との相溶性を顕著に改善
し、諸特性を顕著に向上させる効果を有しているが、そ
の理由としては、ポリエステル系樹脂の末端である水酸
基或いはカルボン酸基と酸無水物基、エポキシ基及びオ
キサゾリン基との反応により、変性ポリスチレン系樹脂
とポリエステル系樹脂とのグラフトポリマーが生成し、
これが界面活性剤的な働きをする事により、ポリエステ
ル系樹脂とポリスチレン系樹脂の相溶性を改善し、非相
溶ミクロ相分離構造を取ることが可能になったためと考
えられる。
0.1 to 20 parts by weight of a modified polystyrene resin is mixed with 100 parts by weight of a resin composition in which a polyester resin and a polystyrene resin are mixed at a predetermined ratio, and the resulting mixture is kneaded by a biaxial kneader or the like. As a result, a thermoplastic resin composition having good compatibility can be obtained. If the amount of the modified polystyrene resin blended is less than 0.1 part by weight, the effect of improving the compatibility becomes insufficient, and if the amount of the modified polystyrene resin blended exceeds 20 parts by weight, the compatibility becomes too good and the characteristics deteriorate. Thus, the modified polystyrene resin of the present invention has the effect of significantly improving the compatibility between the polyester resin and the polystyrene resin, and significantly improving the various properties. A graft polymer of a modified polystyrene-based resin and a polyester-based resin is produced by the reaction of a hydroxyl group or a carboxylic acid group at the terminal of the resin with an acid anhydride group, an epoxy group and an oxazoline group.
It is considered that this acts as a surfactant, which improves the compatibility between the polyester resin and the polystyrene resin and enables the formation of an incompatible microphase-separated structure.

【0010】本発明の熱可塑性樹脂組成物には、更に用
途、目的に応じて他の配合剤、例えばタルク、マイカ、
炭酸カルシウム、ワラストナイトのような無機充填剤、
或いはガラス繊維、カーボン繊維などのような補強剤、
難燃剤、難燃助剤、制電剤、安定剤、顔料、離型剤、酸
化防止剤等を配合することができる。本発明の熱可塑性
樹脂組成物を製造する方法としては、従来から公知の方
法を適用することができ、本発明の熱可塑性樹脂組成物
の原料を一括或いは分割してヘンシェルミキサーにて十
分混合し、更に二軸混練機にて混練することにより得る
ことができる。
The thermoplastic resin composition of the present invention may further contain other compounding agents such as talc, mica, depending on the use and purpose.
Inorganic fillers such as calcium carbonate, wollastonite,
Or reinforcing agents such as glass fiber, carbon fiber, etc.
A flame retardant, a flame retardant aid, an antistatic agent, a stabilizer, a pigment, a release agent, an antioxidant and the like can be added. As a method for producing the thermoplastic resin composition of the present invention, a conventionally known method can be applied, and the raw materials of the thermoplastic resin composition of the present invention are collectively or divided and sufficiently mixed with a Henschel mixer. It can be obtained by further kneading with a biaxial kneader.

【0011】[0011]

【実施例】以下に、実施例を用いて本発明を更に詳細に
示すが、本発明は、これら実施例に限定されるものでは
ない。 《実施例1〜5及び比較例1〜2》表1に示した配合割
合の物をヘンシェルミキサーに投入し、1000〜15
00rpmで数分混合し、これを二軸混練機にて270
〜280℃になるような条件で溶融混練してペレットを
作り、その後射出成形を行い、得られた試験片について
引っ張り強度、引っ張り伸び、アイゾット衝撃強度及び
耐薬品性の評価を行った。その評価結果も表1に示す。
EXAMPLES The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples. << Examples 1 to 5 and Comparative Examples 1 and 2 >> 1000 to 15 were added to the Henschel mixer at the blending ratios shown in Table 1.
Mix for several minutes at 00 rpm, and use a twin-screw kneader for 270
Pellets were prepared by melt-kneading under conditions such that the temperature was up to 280 ° C., and then injection molding was performed, and the obtained test pieces were evaluated for tensile strength, tensile elongation, Izod impact strength and chemical resistance. The evaluation results are also shown in Table 1.

【0012】 [0012]

【0013】*1:ダイヤナイトMA−523V、三菱
レーヨン(株)製 *2:スミブライトM192,住友化学工業(株)製 *3:オキサゾリン基変性ポリスチレン(変性率5wt
%) *4:オキサゾリン基変性ポリスチレン(変性率1wt
%) *5:スチレン−無水マレイン酸共重合体(変性率8w
t%) *6:スチレン−グリシジルメタクリレート共重合体
(変性率5wt%) *7:ASTM D−638に準じて測定した。 *8:1/4”幅のノッチ付き試験片についてASTM
D−256に準じて測定した。 *9:23℃で酢酸ブチル中に引っ張り試験片を3カ月
浸漬し、外観変化を観察した。 表中 ○は使用可能と判断されるもの △は若干侵されるか膨潤したもの ×は使用不可能と判断されるものを示す。
* 1: Dianite MA-523V, manufactured by Mitsubishi Rayon Co., Ltd. * 2: Sumibright M192, manufactured by Sumitomo Chemical Co., Ltd. * 3: Oxazoline group-modified polystyrene (modification rate 5 wt.
%) * 4: Oxazoline group-modified polystyrene (modification rate 1 wt
%) * 5: Styrene-maleic anhydride copolymer (modification rate 8w
t%) * 6: Styrene-glycidyl methacrylate copolymer (modification rate 5 wt%) * 7: Measured according to ASTM D-638. * 8: ASTM for 1/4 "width notched test piece
It measured according to D-256. * 9: The tensile test piece was immersed in butyl acetate at 23 ° C. for 3 months, and the change in appearance was observed. In the table, ◯ indicates that it is usable, and Δ indicates that it is slightly eroded or swollen, and x indicates that it is determined to be unusable.

【0014】[0014]

【発明の効果】表から明らかなように、本発明の熱可塑
性樹脂組成物は、変性ポリスチレン系樹脂を添加するこ
とにより、ポリエステル系樹脂とポリスチレン系樹脂の
相溶性が顕著に改善され、両者の長所を合わせ持つ耐熱
性、耐衝撃性、成形加工性及び耐薬品性に優れる新規で
バランスのとれた材料である。
As is apparent from the table, in the thermoplastic resin composition of the present invention, the compatibility of the polyester resin and the polystyrene resin is remarkably improved by adding the modified polystyrene resin. It is a new and well-balanced material with excellent heat resistance, impact resistance, moldability and chemical resistance.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ポリエステル系樹脂95〜5重量%及び
ポリスチレン系樹脂5〜95重量%から成る樹脂組成物
100重量部に対して、酸無水物基、エポキシ基及びオ
キサゾリン基のうち少なくとも1種の官能基を含有する
変性ポリスチレン系樹脂を0.1〜20重量部添加する
ことを特徴とする熱可塑性樹脂組成物。
1. A resin composition comprising 95 to 5% by weight of a polyester resin and 5 to 95% by weight of a polystyrene resin based on 100 parts by weight of at least one of an acid anhydride group, an epoxy group and an oxazoline group. A thermoplastic resin composition comprising 0.1 to 20 parts by weight of a modified polystyrene resin containing a functional group.
JP13116092A 1992-05-22 1992-05-22 Thermoplastic resin composition Pending JPH05320487A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13116092A JPH05320487A (en) 1992-05-22 1992-05-22 Thermoplastic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13116092A JPH05320487A (en) 1992-05-22 1992-05-22 Thermoplastic resin composition

Publications (1)

Publication Number Publication Date
JPH05320487A true JPH05320487A (en) 1993-12-03

Family

ID=15051410

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13116092A Pending JPH05320487A (en) 1992-05-22 1992-05-22 Thermoplastic resin composition

Country Status (1)

Country Link
JP (1) JPH05320487A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013129547A1 (en) * 2012-02-29 2013-09-06 東レ株式会社 Thermoplastic resin composition and molded article of same
US9464261B2 (en) 2010-05-14 2016-10-11 The Sun Products Corporation Polymer-containing cleaning compositions and methods of production and use thereof
US10005986B2 (en) 2007-02-15 2018-06-26 Ecolab Usa Inc. Fast dissolving solid detergent

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10005986B2 (en) 2007-02-15 2018-06-26 Ecolab Usa Inc. Fast dissolving solid detergent
US9464261B2 (en) 2010-05-14 2016-10-11 The Sun Products Corporation Polymer-containing cleaning compositions and methods of production and use thereof
WO2013129547A1 (en) * 2012-02-29 2013-09-06 東レ株式会社 Thermoplastic resin composition and molded article of same
JP5565523B2 (en) * 2012-02-29 2014-08-06 東レ株式会社 Thermoplastic resin composition and molded article thereof

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