JP2002080728A - Method for producing molded article of thermoplastic resin composition - Google Patents

Method for producing molded article of thermoplastic resin composition

Info

Publication number
JP2002080728A
JP2002080728A JP2000272870A JP2000272870A JP2002080728A JP 2002080728 A JP2002080728 A JP 2002080728A JP 2000272870 A JP2000272870 A JP 2000272870A JP 2000272870 A JP2000272870 A JP 2000272870A JP 2002080728 A JP2002080728 A JP 2002080728A
Authority
JP
Japan
Prior art keywords
temperature
tma
resin
thermoplastic resin
resin composition
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
JP2000272870A
Other languages
Japanese (ja)
Inventor
Satoru Moritomi
悟 森冨
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 Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP2000272870A priority Critical patent/JP2002080728A/en
Publication of JP2002080728A publication Critical patent/JP2002080728A/en
Pending legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a method for producing a molded article of a thermoplastic resin composition composed of a thermoplastic resin composition containing a crystalline resin and an amorphous resin and having excellent chemical resistance and appearance. SOLUTION: The method for producing a molded article of a thermoplastic resin composition containing (A) a crystalline resin and (B) an amorphous resin having a glass transition temperature lower than the melting temperature of the resin A and forming a continuous phase at an A/B weight ratio of 1/99 to 60/40 comprises the molding of the composition under a condition satisfying the formula: Tma>Tf>=[Tma-(Tma-Tg)/3] wherein Tf is the molding temperature, Tma is the melting temperature of the component A and Tg is the glass transition temperature of the component B.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、熱可塑性樹脂組成
物成形体の製造方法の製造方法に関するものである。更
に詳しくは、本発明は、結晶性樹脂並びに非晶性樹脂を
含む熱可塑性樹脂組成物からなり、耐薬品性に優れ、か
つ外観に優れた熱可塑性樹脂組成物成形体の製造方法に
関するものである。
The present invention relates to a method for producing a molded article of a thermoplastic resin composition. More specifically, the present invention relates to a method for producing a molded article of a thermoplastic resin composition comprising a thermoplastic resin composition containing a crystalline resin and an amorphous resin, and having excellent chemical resistance and excellent appearance. is there.

【0002】[0002]

【従来の技術】たとえば、ポリフェニレンエーテル系樹
脂、ポリスチレン系樹脂等の非晶性樹脂は、寸法安定性
等に優れ、成形品の形状安定性という観点からは優れて
いるが、有機溶媒、各種オイル、洗剤等の薬品に対する
耐性が低いため、耐薬品性が要求される用途には不適で
あった。この欠点を補うために非晶性樹脂に結晶性樹脂
を添加する技術が開示されている。たとえば、ポリフェ
ニレンエーテル系樹脂にシンジオタクチック構造を有す
るアルケニル芳香族系樹脂を添加する技術が特開平02
−64140号公報に開示されている。しかしながら、
単にポリフェニレンエーテル系樹脂添加しても、シンジ
オタクチック構造を有するアルケニル芳香族系樹脂が結
晶化し難く、耐薬品性の改善は図れない。かかる問題を
解決するために射出成形時の金型温度を(シンジオタク
チック構造を有するアルケニル芳香族系樹脂のガラス転
移温度−10℃)以上(シンジオタクチック構造を有す
るアルケニル芳香族系樹脂の溶融温度+10℃)以下に
高周波誘導加熱する技術が特開平11−5236号公報
に開示されてるが、結晶化度を十分には高めることがで
きず、耐溶剤性の改良効果が小さい。さらに、射出成形
時の金型温度が高い場合、成形品を取り出すまでの冷却
時間が長くなり、生産性が悪化するという欠点がある。
2. Description of the Related Art For example, amorphous resins such as polyphenylene ether-based resins and polystyrene-based resins are excellent in dimensional stability and the like, and are excellent from the viewpoint of shape stability of molded articles. In addition, it has low resistance to chemicals such as detergents, and is not suitable for applications requiring chemical resistance. A technique for adding a crystalline resin to an amorphous resin to make up for this drawback has been disclosed. For example, a technique of adding an alkenyl aromatic resin having a syndiotactic structure to a polyphenylene ether resin is disclosed in
-64140. However,
Even if a polyphenylene ether-based resin is simply added, the alkenyl aromatic resin having a syndiotactic structure is hardly crystallized, and improvement in chemical resistance cannot be achieved. In order to solve such a problem, the mold temperature at the time of injection molding must be equal to or higher than (glass transition temperature of alkenyl aromatic resin having a syndiotactic structure −10 ° C.) (melting of alkenyl aromatic resin having a syndiotactic structure). Japanese Patent Application Laid-Open No. H11-5236 discloses a technique for performing high-frequency induction heating at a temperature of + 10 ° C. or lower, but cannot sufficiently increase the crystallinity, and has a small effect of improving solvent resistance. Furthermore, when the temperature of the mold during injection molding is high, there is a disadvantage that the cooling time until the molded product is taken out becomes long, and the productivity is deteriorated.

【0003】[0003]

【発明が解決しようとする課題】かかる状況に鑑み、本
発明が解決しようとする課題は、結晶性樹脂並びに非晶
性樹脂を含む熱可塑性樹脂組成物からなり、耐薬品性に
優れ、かつ外観に優れた熱可塑性樹脂組成物成形体の製
造方法を提供する点にある。
SUMMARY OF THE INVENTION In view of such circumstances, an object of the present invention is to provide a thermoplastic resin composition containing a crystalline resin and an amorphous resin, which has excellent chemical resistance and appearance. Another object of the present invention is to provide a method for producing a molded article of a thermoplastic resin composition having excellent heat resistance.

【0004】[0004]

【課題を解決するための手段】すなわち、本発明は、下
記の成分である(A)及び(B)を(A)/(B)の重
量比で1/99〜60/40の割合で含有し、(B)が
連続相を形成した熱可塑性樹脂組成物からなる成形体の
製造方法であって、下記式(1)の条件下に成形する熱
可塑性樹脂組成物成形体の製造方法に係るものである。 (A):結晶性樹脂 (B):ガラス転移温度が(A)の溶融温度より低い非
晶性樹脂 Tma > Tf ≧〔Tma−(Tma−Tg)/3〕 (1) ただし、Tfは成形温度を表し、Tmaは成分(A)の
融解温度を表し、Tgは成分(B)のガラス転移温度を
表す。
That is, the present invention comprises the following components (A) and (B) at a weight ratio of (A) / (B) of 1/99 to 60/40. (B) is a method for producing a molded article made of a thermoplastic resin composition in which a continuous phase is formed, and relates to a method for producing a molded article of a thermoplastic resin composition molded under the conditions of the following formula (1). Things. (A): crystalline resin (B): amorphous resin having a glass transition temperature lower than the melting temperature of (A) Tma> Tf ≧ [Tma− (Tma−Tg) / 3] (1) where Tf is a molding Represents temperature, Tma represents the melting temperature of component (A), and Tg represents the glass transition temperature of component (B).

【0005】[0005]

【発明の実施の形態】(A)成分は、結晶性樹脂であ
り、シンジオタクチック構造を有するアルケニル芳香族
系樹脂、ポリエチレンテレフタレート系樹脂、ポリブチ
レンテレフタレート系樹脂、ポリエーテルエーテルケト
ン系樹脂、ポリアセタール系樹脂、ポリアミド系樹脂、
ポリプロピレン系樹脂、ポリエチレン系樹脂、ポリフェ
ニレンスルフィド系樹脂等が例示される。
DETAILED DESCRIPTION OF THE INVENTION The component (A) is a crystalline resin, which is an alkenyl aromatic resin having a syndiotactic structure, a polyethylene terephthalate resin, a polybutylene terephthalate resin, a polyether ether ketone resin, and a polyacetal. Resin, polyamide resin,
Examples thereof include a polypropylene resin, a polyethylene resin, and a polyphenylene sulfide resin.

【0006】(B)成分は、ガラス転移温度が(A)の
溶融温度より低い非晶性樹脂である。非晶性樹脂として
は、ポリフェニレンエーテル系樹脂、ポリスチレン系樹
脂、ポリカーボネート系樹脂、ポリエーテルサルホン系
樹脂、ポリエーテルイミド系樹脂、アクリロニトリル-
ブタジエン-スチレン系樹脂(ABS系樹脂)、ポリス
ルホン系樹脂、ポリメチルメタクリレート系樹脂等が例
示される。
The component (B) is an amorphous resin having a glass transition temperature lower than the melting temperature of the component (A). As the amorphous resin, polyphenylene ether resin, polystyrene resin, polycarbonate resin, polyether sulfone resin, polyetherimide resin, acrylonitrile-
Examples thereof include butadiene-styrene resin (ABS resin), polysulfone resin, and polymethyl methacrylate resin.

【0007】(A)と(B)については、種々の組み合
わせのものを使用し得る。また、(A)として複数の結
晶性樹脂を組み合わせて使用することができる。(B)
として相溶する複数の非晶性樹脂を組み合わせて使用す
ることができる。ここでいう相溶とは、混合した際、単
一のガラス転移温度を示すことを示す。
As for (A) and (B), various combinations can be used. Further, a plurality of crystalline resins can be used in combination as (A). (B)
A plurality of amorphous resins compatible with each other can be used in combination. The term "compatible" as used herein means that when mixed, it shows a single glass transition temperature.

【0008】本発明の熱可塑性樹脂組成物は、(B)ガ
ラス転移温度が(A)の溶融温度より低い必要がある。
(A)の融解温度および(B)のガラス転移温度は、J
ISK7121に準拠し、測定される。ただし、(A)
として複数の結晶性樹脂を使用する場合、それらの融解
温度のうち最も高い融解温度を示す。(B)のガラス転
移温度が(A)溶融温度より高い場合、(A)の融解温
度未満の温度で成形することが、困難である。
[0008] The thermoplastic resin composition of the present invention must have (B) a glass transition temperature lower than the melting temperature of (A).
The melting temperature of (A) and the glass transition temperature of (B) are J
Measured according to ISK7121. However, (A)
When a plurality of crystalline resins are used, the highest melting temperature among those melting temperatures is shown. When the glass transition temperature of (B) is higher than the melting temperature of (A), it is difficult to mold at a temperature lower than the melting temperature of (A).

【0009】本発明の熱可塑性樹脂組成物は、(B)が
連続相を形成している必要がある。(B)が連続相を形
成しない場合、(A)の融解温度以下での流動性が低下
し、(A)の融解温度未満での成形が困難になる。
In the thermoplastic resin composition of the present invention, (B) needs to form a continuous phase. If (B) does not form a continuous phase, the fluidity below the melting temperature of (A) is reduced, and molding below the melting temperature of (A) becomes difficult.

【0010】本発明の熱可塑性樹脂組成物は、(A)及
び(B)を(A)/(B)の重量比で1/99〜60/
40の割合で含有するものであり、好ましくは3/97
〜40/60の割合で含有するものである。(A)が過
少な場合、耐薬品性改良効果が乏しくなる。一方、
(A)が過多の場合、耐熱性が悪化する。
In the thermoplastic resin composition of the present invention, the weight ratio of (A) and (B) to (A) / (B) is from 1/99 to 60 /
40, preferably 3/97
4040/60. If (A) is too small, the effect of improving chemical resistance is poor. on the other hand,
When (A) is excessive, heat resistance is deteriorated.

【0011】本発明の熱可塑性樹脂組成物は、染料、顔
料、帯電防止剤、滑剤、酸化防止剤、耐候性付与剤等を
添加することができる。更に、本発明の熱可塑性樹脂組
成物は、珪酸カルシウム、珪酸マグネシウム、ガラス繊
維、金属ウィスカー、シリカ、炭酸カルシウム、ワラス
トナイト、タルク、マイカ、カオリン等の無機フィラー
を添加することができる。更に、連続相を形成しない非
晶性樹脂を添加することができる。
The thermoplastic resin composition of the present invention may contain dyes, pigments, antistatic agents, lubricants, antioxidants, weathering agents and the like. Further, the thermoplastic resin composition of the present invention may contain an inorganic filler such as calcium silicate, magnesium silicate, glass fiber, metal whisker, silica, calcium carbonate, wollastonite, talc, mica, and kaolin. Further, an amorphous resin that does not form a continuous phase can be added.

【0012】本発明の熱可塑性樹脂組成物の製造法は特
に限定されないが、たとえば、溶液ブレンド法、溶融混
練法等の各種方法があげられる。これらの中では、溶融
混練法が好ましい。具体的な方法としては、各成分をバ
ンバリーミキサー、プラストミル、ブラベンダー、一軸
又は二軸の押し出し幾等の公知の混練機で溶融混練する
方法を例示しうる。混練に際して、混練温度は、通常1
50〜400℃、好ましくは200〜350℃の範囲が
選ばれる。
[0012] The method for producing the thermoplastic resin composition of the present invention is not particularly limited, and examples thereof include various methods such as a solution blending method and a melt kneading method. Among these, the melt kneading method is preferred. As a specific method, a method in which each component is melt-kneaded by a known kneading machine such as a Banbury mixer, a plast mill, a Brabender, a single-screw or twin-screw extruder, or the like can be exemplified. In kneading, the kneading temperature is usually 1
A range of 50 to 400C, preferably 200 to 350C is selected.

【0013】本発明の熱可塑性樹脂組成物成形体の製造
方法は、下記式(1)の条件下に成形することを特徴と
する。 Tma>Tf≧〔Tma−{(Tma−Tg)/3}〕 (1) ただし、Tfは成形温度を表し、Tmaは成分(A)の
融解温度を表し、Tgは成分(B)のガラス転移温度を
表す。
The method for producing a molded article of the thermoplastic resin composition of the present invention is characterized in that the molded article is molded under the condition of the following formula (1). Tma> Tf ≧ [Tma-{(Tma-Tg) / 3}] (1) where Tf represents a molding temperature, Tma represents a melting temperature of the component (A), and Tg is a glass transition of the component (B). Represents temperature.

【0014】成形方法が射出成形の場合又は押出成形の
場合、Tfは射出成形機又は押出機のシリンダー温度に
相当する。一般的に、シリンダー温度は複数のゾーン毎
に設定することが可能であるが、全シリンダーの1/2
以上の領域を上記式(1)の温度範囲にする必要があ
る。成形方法がプレス成形の場合、Tfはプレス金型の
温度に相当し、実質的に全面を上記式(1)の温度範囲
にすることが必要である。成形方法がカレンダー成形の
場合、Tfはカレンダーロールの設定温度に相当する。
カレンダー成形においては、一般的に3本以上のカレン
ダーロールが用いられるが、1/2以上の本数のロール
を上記式(1)の温度範囲にすることが必要である。
When the molding method is injection molding or extrusion molding, Tf corresponds to the cylinder temperature of the injection molding machine or extruder. Generally, the cylinder temperature can be set for each of a plurality of zones.
It is necessary to set the above region to the temperature range of the above equation (1). When the molding method is press molding, Tf corresponds to the temperature of the press die, and it is necessary to substantially keep the entire surface within the temperature range of the above formula (1). When the molding method is calender molding, Tf corresponds to the set temperature of the calender roll.
In calendering, generally three or more calender rolls are used, but it is necessary that the number of rolls equal to or more than 1/2 be within the temperature range of the above formula (1).

【0015】本発明の熱可塑性樹脂組成物成形体の製造
に用いられる成形方法は、前記の成形方法に限定されな
いが、金型内部以外における溶融樹脂の流動を伴う成形
方法の場合、溶融樹脂の流路の1/2以上の領域の温度
を上記式(1)の温度範囲にすることが必要であり、金
型内部以外における樹脂の流動を伴わない成形方法の場
合、溶融樹脂が接触する金型部分の温度を上記式(1)
の温度範囲に設定することが必要である。
The molding method used for producing the molded article of the thermoplastic resin composition of the present invention is not limited to the above-mentioned molding method. It is necessary to set the temperature of a region of at least half of the flow path to the temperature range of the above formula (1). The temperature of the mold part is calculated by the above equation (1).
It is necessary to set the temperature range.

【0016】TfがTmaがより高い場合は、(A)成
分の結晶化が十分に進行せず、耐薬品性の改良効果が乏
しくなる。また、Tfが〔Tma−{(Tma−Tg)
/3}〕より低い場合は樹脂組成物の流動性が乏しくな
り、成形品の外観が悪化したり、成形が困難になる。す
なわち、本発明の上記式(1)の条件を採用することに
より、(A)成分の結晶化が促進され、耐薬品性が向上
し、かつ良好な外観の成形品を得ることができるのであ
る。
When Tf is higher than Tma, the crystallization of the component (A) does not proceed sufficiently, and the effect of improving the chemical resistance is poor. Further, when Tf is [Tma-{(Tma-Tg)
/ 3}]], the fluidity of the resin composition is poor, the appearance of the molded product is deteriorated, and molding becomes difficult. That is, by adopting the condition of the above formula (1) of the present invention, crystallization of the component (A) is promoted, chemical resistance is improved, and a molded article having a good appearance can be obtained. .

【0017】本発明の成形品は、耐薬品性が要求される
分野、たとえば、フライバックトランス、偏向ヨーク等
の電気・電子部品用途、電子レンジ等の周辺部品用途、
ポンプ、タンク、ダクト等の給排水・給排気部品用途、
バッテリケース等の電槽用途、水道量水器、現像タン
ク、ファン及びファンハウジング等に使用することがで
きる。更に、インストルメンタルパネル、ホイルカバ
ー、ヒューズホルダー、ラジエーターグリル、イグニッ
ションコイル、サイドマッドガード、バンパー等の自動
車用途、OA機器のハウジング、OA機器のシャーシ、
トレー等の機構部品用途、自動販売機のコインメカシャ
ーシ等に使用することができる。
The molded article of the present invention is used in fields where chemical resistance is required, for example, electric / electronic parts such as flyback transformers and deflection yokes, peripheral parts such as microwave ovens, etc.
For water supply / drainage / supply / exhaust parts such as pumps, tanks, ducts, etc.
It can be used for battery cases and other battery cases, tap water dispensers, developing tanks, fans and fan housings. In addition, automotive applications such as instrument panels, wheel covers, fuse holders, radiator grills, ignition coils, side mudguards, bumpers, etc., housings for OA equipment, chassis for OA equipment,
It can be used for mechanical parts such as trays and coin mechanical chassis of vending machines.

【0018】[0018]

【実施例】以下、実施例に基づいて本発明をさらに詳し
く説明するが、本発明はこれらの実施例に限定されるも
のではない。以下に実施例および比較例で使用した略号
の意味を示す。 (A)成分:PA ポリアミド66樹脂 商標 CM3
007(東レ(株)製)融解温度255℃ (B)成分:HIPS ハイインパクトポリスチレン樹
脂 商標 スミブライトH554(日本ポリスチレン
(株)製) (B)成分:SMA 無水マレイン酸含有量約8%の
スチレン-無水マレイン酸共重合体 商標 ダイラーク
232(ノバ・ケミカル・ジャパン販売)
The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples. The meanings of the abbreviations used in Examples and Comparative Examples are shown below. Component (A): PA polyamide 66 resin Trademark CM3
007 (manufactured by Toray Industries, Inc.) Melting temperature 255 ° C. (B) component: HIPS high impact polystyrene resin Trademark Sumibrite H554 (manufactured by Nippon Polystyrene Co., Ltd.) (B) component: SMA Styrene having a maleic anhydride content of about 8% -Maleic anhydride copolymer trademark DAILARK 232 (sold by Nova Chemical Japan)

【0019】参考例1:組成物1の製造 PA10wt%、HIPS80wt%、SMA10wt
%を二軸混練機TEM50A(東芝機械(株)製)に
て、シリンダー温度280℃、スクリュー回転数200
rpmの条件にて溶融混練し、ダイから押し出した後、
水槽にて冷却し、ストランドカッターにてペレット化
し、組成物1を得た。組成物1の連続相は、HIPSと
SMAとの相溶物であった。
Reference Example 1 Preparation of Composition 1 PA 10 wt%, HIPS 80 wt%, SMA 10 wt%
% In a twin-screw kneader TEM50A (manufactured by Toshiba Machine Co., Ltd.), cylinder temperature 280 ° C., screw rotation speed 200
After melt-kneading under the condition of rpm and extruding from the die,
The mixture was cooled in a water tank and pelletized with a strand cutter to obtain Composition 1. The continuous phase of Composition 1 was a compatible product of HIPS and SMA.

【0020】(B)成分のガラス転移温度 HIPS88.8wt%とSMA11.1wt%とを二
軸混練機TEM50A(東芝機械(株)製)にて、シリ
ンダー温度230℃、スクリュー回転数200rpmの
条件にて溶融混練し、ダイから押し出した後、水槽にて
冷却し、ストランドカッターにてペレット化し、組成物
を得た。示差走査型熱量計にて、20℃から200℃ま
で、10℃/minにて昇温し、JIS K7121に
準拠し組成物のガラス転移温度を測定した。組成物は単
一のガラス転移温度を示し、HIPSとSMAが相溶し
ていることを確認した。組成物のガラス転移温度は10
2℃であった。
The glass transition temperature HIPS ( 88.8 wt%) and SMA 11.1 wt% of the component (B) are mixed in a twin-screw kneader TEM50A (manufactured by Toshiba Machine Co., Ltd.) under the conditions of a cylinder temperature of 230 ° C. and a screw rotation speed of 200 rpm. After melt-kneading and extruding from a die, the mixture was cooled in a water bath and pelletized with a strand cutter to obtain a composition. The temperature was raised at a rate of 10 ° C./min from 20 ° C. to 200 ° C. using a differential scanning calorimeter, and the glass transition temperature of the composition was measured in accordance with JIS K7121. The composition exhibited a single glass transition temperature, confirming that HIPS and SMA were compatible. The glass transition temperature of the composition is 10
2 ° C.

【0021】物性値等の評価方法を以下に示す。成形品の結晶化度の評価 各成形品からサンプルを切り出し、20℃から300℃
まで10℃/minで昇温し、JIS K7121に準
拠し、255℃付近のPAの結晶融解に起因する吸熱ピ
ークの温度および融解熱量ΔH(J/g)を測定した。耐薬品性評価 各成形品を23℃にて、曲率が168mmの半円状治具
に取り付け、試験片中央部に、サラダ油をしみ込ませた
20×12mmのガーゼを置き、60分後にクラック発
生の有無を目視にて評価した。60分後のクラック発生
状態を、○(クラック発生せず)、×(クラック発生あ
り)とした。
The methods for evaluating physical properties and the like are described below. Evaluation of crystallinity of molded products Samples were cut out from each molded product, and 20 to 300 ° C.
Then, the temperature was raised at 10 ° C./min, and the endothermic peak temperature and heat of fusion ΔH (J / g) at around 255 ° C. due to the PA crystal melting were measured in accordance with JIS K7121. Evaluation of chemical resistance Each molded product was attached to a semicircular jig having a curvature of 168 mm at 23 ° C., and a 20 × 12 mm gauze impregnated with salad oil was placed in the center of the test piece, and cracks were generated 60 minutes later. The presence or absence was visually evaluated. The state of occurrence of cracks after 60 minutes was evaluated as ○ (no crack occurred) and X (crack occurred).

【0022】実施例1 シリンダーの温度設定域が上流からC1、C2、C3、
C4の4ゾーンに分かれた射出成形機(サイキャップ1
10/50 住友重機械工業製)を用い、C1〜C4の
温度をともに240℃にし、金型温度50℃にて、熱可
塑性樹脂組成物1を射出成形し、ASTM引張1号ダン
ベルを得た。得られた試験片を用い、ΔHの測定、耐薬
品性試験、外観評価を実施した。結果を表1に示す。 実施例2、比較例1及び比較例2 表1に示す組成物、成形条件以外は、実施例1と同様に
評価を行った。結果を表1に示す。
Embodiment 1 C1, C2, C3, C3, C3
Injection molding machine (Cycap 1) divided into four zones of C4
10/50, manufactured by Sumitomo Heavy Industries, Ltd., the C1 to C4 temperatures were both set to 240 ° C., and at a mold temperature of 50 ° C., the thermoplastic resin composition 1 was injection molded to obtain an ASTM tensile No. 1 dumbbell. . Using the obtained test pieces, measurement of ΔH, chemical resistance test, and appearance evaluation were performed. Table 1 shows the results. Example 2, Comparative Example 1, and Comparative Example 2 Evaluation was performed in the same manner as in Example 1 except for the composition and molding conditions shown in Table 1. Table 1 shows the results.

【0023】[0023]

【表1】 *1:〔Tma−{(Tma−Tg)/3}〕[Table 1] * 1: [Tma-{(Tma-Tg) / 3}]

【0024】[0024]

【発明の効果】以上説明したとおり、本発明により、結
晶性樹脂並びに非晶性を含む熱可塑性樹脂組成物からな
り、耐薬品性に優れ、かつ外観に優れた熱可塑性樹脂組
成物成形体の製造方法を提供することができた。
As described above, according to the present invention, a molded article of a thermoplastic resin composition comprising a crystalline resin and a thermoplastic resin composition containing an amorphous material, having excellent chemical resistance and excellent appearance. A manufacturing method could be provided.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4F071 AA22 AA36 AA45 AA84 AA86 AH19 BB05 BC07 4F206 AA13 AA29 AR06 JA07 JF01 JQ41 JQ46 4J002 BB03X BB12X BC03W BG06W BN15W CB00X CF06X CF07X CG01W CH07W CH09X CL00X CM04W CN01X CN03W GN00 GQ00  ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4F071 AA22 AA36 AA45 AA84 AA86 AH19 BB05 BC07 4F206 AA13 AA29 AR06 JA07 JF01 JQ41 JQ46 4J002 BB03X BB12X BC03W BG06W BN15W CB00X CF06X CH07XCN01 CNW

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 下記の成分である(A)及び(B)を
(A)/(B)の重量比で1/99〜60/40の割合
で含有し、(B)が連続相を形成した熱可塑性樹脂組成
物からなる成形体の製造方法であって、下記式(1)の
条件下に成形する熱可塑性樹脂組成物成形体の製造方
法。 (A):結晶性樹脂 (B):ガラス転移温度が(A)の溶融温度より低い非
晶性樹脂 Tma>Tf≧〔Tma−(Tma−Tg)/3〕 (1) ただし、Tfは成形温度を表し、Tmaは成分(A)の
融解温度を表し、Tgは成分(B)のガラス転移温度を
表す。
1. The following components (A) and (B) are contained at a weight ratio of (A) / (B) of 1/99 to 60/40, and (B) forms a continuous phase. A method for producing a molded article made of the thermoplastic resin composition, wherein the molded article is molded under the condition of the following formula (1). (A): crystalline resin (B): amorphous resin whose glass transition temperature is lower than the melting temperature of (A) Tma> Tf ≧ [Tma− (Tma−Tg) / 3] (1) where Tf is a molding Represents temperature, Tma represents the melting temperature of component (A), and Tg represents the glass transition temperature of component (B).
JP2000272870A 2000-09-08 2000-09-08 Method for producing molded article of thermoplastic resin composition Pending JP2002080728A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000272870A JP2002080728A (en) 2000-09-08 2000-09-08 Method for producing molded article of thermoplastic resin composition

Publications (1)

Publication Number Publication Date
JP2002080728A true JP2002080728A (en) 2002-03-19

Family

ID=18758920

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2002080728A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004536942A (en) * 2001-08-01 2004-12-09 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Molding compositions formed from glassy and semi-crystalline polymers
DE102019133586B4 (en) 2019-12-09 2024-07-18 Bombardier Transportation Gmbh Rail vehicle wagon with an interior fitting fixed to the wagon body

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07314519A (en) * 1994-05-30 1995-12-05 Hitachi Chem Co Ltd Production of matted thermoplastic resin molding
JPH0931207A (en) * 1995-07-19 1997-02-04 Asahi Chem Ind Co Ltd Production of thermoplastic polymer molded product having marble-like pattern
JP2001170984A (en) * 1999-12-17 2001-06-26 Hitachi Chem Co Ltd Method for producing thermoplastic resin sheet

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07314519A (en) * 1994-05-30 1995-12-05 Hitachi Chem Co Ltd Production of matted thermoplastic resin molding
JPH0931207A (en) * 1995-07-19 1997-02-04 Asahi Chem Ind Co Ltd Production of thermoplastic polymer molded product having marble-like pattern
JP2001170984A (en) * 1999-12-17 2001-06-26 Hitachi Chem Co Ltd Method for producing thermoplastic resin sheet

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004536942A (en) * 2001-08-01 2004-12-09 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Molding compositions formed from glassy and semi-crystalline polymers
DE102019133586B4 (en) 2019-12-09 2024-07-18 Bombardier Transportation Gmbh Rail vehicle wagon with an interior fitting fixed to the wagon body

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