JPH05171040A - Resin composition containing liquid crystal polyester - Google Patents

Resin composition containing liquid crystal polyester

Info

Publication number
JPH05171040A
JPH05171040A JP35618291A JP35618291A JPH05171040A JP H05171040 A JPH05171040 A JP H05171040A JP 35618291 A JP35618291 A JP 35618291A JP 35618291 A JP35618291 A JP 35618291A JP H05171040 A JPH05171040 A JP H05171040A
Authority
JP
Japan
Prior art keywords
resin
liquid crystal
crystal polyester
weight
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
JP35618291A
Other languages
Japanese (ja)
Inventor
Kazunari Inoue
一成 井上
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.)
SABIC Innovative Plastics Japan KK
Original Assignee
GE Plastics Japan 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 GE Plastics Japan Ltd filed Critical GE Plastics Japan Ltd
Priority to JP35618291A priority Critical patent/JPH05171040A/en
Publication of JPH05171040A publication Critical patent/JPH05171040A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a resin compsn. lowered in melt viscosity and hence improved in moldability by blending a polyetherimide resin with a thermotropic liquid crystal polyester and a polycarbonate resin. CONSTITUTION:The title compsn, comprises (A) 60-99 pts.wt. polyether-imide resin, (B) 1-40 pts.wt. thermotropic liquid crystal polyester, and (C) a polycarbonate resin, the amt. of which is 3-50 pts.wt. per 100 pts.wt. sum of (A) and (B). Conventionall methods are satisfactorily used in the preparation of this resin compsn., but the melt milling method is generally preferable. This resin compsn. is a polyether-imide resin compsn. improved in melt viscosity without lowering of mechanical properties and without delamination.

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、サーモトロピック液晶
ポリエステルを含む、ポリエーテルイミド(以下、PE
Iということがある)系樹脂組成物に関し、さらに詳し
くは、PEI系樹脂、サーモトロピック液晶ポリエステ
ルおよびポリカーボネート系樹脂を含む樹脂組成物に関
する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polyetherimide (hereinafter PE) containing a thermotropic liquid crystal polyester.
I)) based resin composition, and more specifically, to a resin composition containing a PEI based resin, a thermotropic liquid crystal polyester and a polycarbonate based resin.

【0002】[0002]

【従来の技術】ポリエーテルイミドは、優れた耐炎性、
機械的強度および耐熱性を有するので、高性能の熱可塑
性成形材料として各種用途に使用されている。しかし、
使用されているポリエーテルイミドは、溶融されたとき
に高い粘度を示すので加工性が悪く、粘度を下げるため
に高い加工温度を必要とする、この問題を避けるために
低重合度のポリエーテルイミドを用いることが考えられ
るが、すると耐薬品性、機械的強度などが損なわれ、満
足な物性の成形品が得られない。
2. Description of the Related Art Polyetherimide has excellent flame resistance,
Since it has mechanical strength and heat resistance, it is used in various applications as a high-performance thermoplastic molding material. But,
The polyetherimide used has poor processability because it exhibits a high viscosity when melted, and requires a high processing temperature to reduce the viscosity. To avoid this problem, a polyetherimide having a low polymerization degree is used. However, chemical resistance, mechanical strength, etc. are impaired, and a molded product having satisfactory physical properties cannot be obtained.

【0003】加工性の改善のために金属石鹸、脂肪酸ア
ミド等の化合物を少量配合することが提案されている
(特開平1-139645号公報)。しかし、少量では効果が少
なく、また加工温度によってはシルバーストリークを生
じやすいので、この方法は十分とはいえない。
It has been proposed to add a small amount of a compound such as a metal soap or a fatty acid amide in order to improve workability (JP-A-1-139645). However, this method is not sufficient because a small amount is not effective and silver streak is likely to occur depending on the processing temperature.

【0004】また液晶ポリマーを配合することも知られ
ている(特開昭63-215769 号公報)。しかし、みかけの
粘度は低下するものの、液晶ポリマーとポリエーテルイ
ミドとは相溶性が悪く、成形品は層状剥離を示すので、
実用には不向きである。
It is also known to compound a liquid crystal polymer (Japanese Patent Laid-Open No. 63-215769). However, although the apparent viscosity is lowered, the compatibility between the liquid crystal polymer and the polyetherimide is poor, and the molded product exhibits layered peeling,
Not suitable for practical use.

【0005】[0005]

【発明が解決しようとする課題】そこで本発明は、ポリ
エーテルイミドの高い溶融粘度に起因する加工性の問題
を解決することを目的とする。
The object of the present invention is therefore to solve the problem of processability due to the high melt viscosity of polyetherimide.

【0006】[0006]

【課題を解決するための手段】本発明者らは、ポリエー
テルイミドの溶融流動性の改善について鋭意検討を重ね
た結果、ポリエーテルイミド樹脂とサーモトロピック液
晶ポリエステルのブレンドに、さらにポリカーボネート
系樹脂を配合して得られた樹脂組成物は、樹脂同志の分
散性が良いので、溶融粘度が低下して成形加工性が改善
されることを見出し、本発明に到達した。
Means for Solving the Problems As a result of intensive studies on the improvement of the melt flowability of polyetherimide, the inventors of the present invention have found that a blend of a polyetherimide resin and a thermotropic liquid crystal polyester further contains a polycarbonate resin. Since the resin composition obtained by blending has good dispersibility between resins, it was found that the melt viscosity is lowered and the moldability is improved, and the present invention has been accomplished.

【0007】すなわち本発明は、(A)ポリエーテルイ
ミド系樹脂 60〜99重量部および(B)サーモトロ
ピック液晶ポリエステル 1〜40重量部を含み、さら
に(A)および(B)の合計100重量部に対して
(C)ポリカーボネート系樹脂 3〜50重量部を含む
樹脂組成物を提供するものである。
That is, the present invention comprises (A) 60 to 99 parts by weight of a polyetherimide resin and (B) 1 to 40 parts by weight of a thermotropic liquid crystal polyester, and further 100 parts by weight of (A) and (B) in total. On the other hand, a resin composition containing 3 to 50 parts by weight of (C) a polycarbonate-based resin is provided.

【0008】本発明で使用する(A)PEI系樹脂は、
下記式(化1):
The (A) PEI resin used in the present invention is
The following formula (Formula 1):

【0009】[0009]

【化1】 (式中、R1 は炭素原子数6〜30の二価の芳香族有機
基、R2 は炭素原子数6〜30の二価の芳香族有機基、
炭素原子数2〜20のアルキレン基もしくはシクロアル
キレン基または炭素原子数2〜8のアルキレン基で連鎖
停止されたポリオルガノシロキサン基を表す)で示され
る繰り返し単位を有する重合体である。
[Chemical 1] (In the formula, R 1 is a divalent aromatic organic group having 6 to 30 carbon atoms, R 2 is a divalent aromatic organic group having 6 to 30 carbon atoms,
A polymer having a repeating unit represented by an alkylene group having 2 to 20 carbon atoms, a cycloalkylene group, or a polyorganosiloxane group chain-terminated with an alkylene group having 2 to 8 carbon atoms).

【0010】ここでR1 としては、具体的には次式(化
2):
Here, as R 1 , specifically, the following formula (Formula 2):

【0011】[0011]

【化2】 で示される群の基が挙げられる。[Chemical 2] The group of the group shown by is mentioned.

【0012】特に典型的なポリエーテルイミド系樹脂と
しては、下記式(化3):
A particularly typical polyetherimide resin is represented by the following formula (Formula 3):

【0013】[0013]

【化3】 で示されるものが挙げられ、これはゼネラルエレクトリ
ック社より”ULTEM”の商品名で市販されている。
[Chemical 3] , Which is commercially available under the trade name of "ULTEM" from General Electric Company.

【0014】次に、(B)サーモトロピック液晶ポリエ
ステルは、下記構造を有するセグメントを含むポリエス
テルの群より選択することができる。
Next, the thermotropic liquid crystal polyester (B) can be selected from the group of polyesters containing a segment having the following structure.

【0015】−O−R−O− −CO−R−CO− −O−R−CO− ここでRは、それぞれ下記(化4)の群より選択するこ
とができる。
--OR--O-- --CO--R--CO-- --ORR--CO-- Here, each R can be selected from the group of the following (Chemical Formula 4).

【0016】[0016]

【化4】 また、上記Rにおける芳香環、脂肪族基、脂環族基等は
以下(化5)の群より選択される置換基によって置換さ
れていてもよい。
[Chemical 4] Further, the aromatic ring, aliphatic group, alicyclic group and the like in R may be substituted with a substituent selected from the group of the following (Chemical Formula 5).

【0017】[0017]

【化5】 上記の成分(B)は、成分(A)60〜99重量部に対
して1〜40重量部、好ましくは(A)70〜97重量
部に対して3〜30重量部配合される。成分(B)が1
重量部未満の場合には溶融流動性の向上効果が少なく、
また40重量部より多いと層状剥離を生じやすくなる。
[Chemical 5] The component (B) is blended in an amount of 1 to 40 parts by weight, preferably 70 to 97 parts by weight of the component (A), in an amount of 3 to 30 parts by weight. Ingredient (B) is 1
If it is less than part by weight, the effect of improving melt fluidity is small,
If the amount is more than 40 parts by weight, delamination is likely to occur.

【0018】本発明に使用される(C)ポリカーボネー
ト系樹脂は、公知のホスゲン法または溶融法により作ら
れた芳香族ポリカーボネートである(例えば特開昭63-2
15763 号公報および特開平2-124934号公報参照)。ポ
リカーボネート系樹脂は、カーボネート成分およびジフ
ェノール成分よりなる。カーボネート成分を導入するた
めの前駆物質としては、例えばホスゲン、ジフェニルカ
ーボネート等が挙げられる。また、適したジフェノール
としては、例えば2,2-ビス(4-ヒドロキシフェニル)プ
ロパン(いわゆるビスフェノールA);2,2-ビス(3,5-
ジブロモ-4- ヒドロキシフェニル)プロパン;2,2-ビス
(3,5-ジメチル-4- ヒドロキシフェニル)プロパン;1,
1-ビス(4-ヒドロキシフェニル)シクロヘキサン;1,1-
ビス(3,5-ジメチル-4- ヒドロキシフェニル)シクロヘ
キサン;1,1-ビス(4-ヒドロキシフェニル)デカン;1,
4-ビス(4-ヒドロキシフェニル)プロパン;1,1-ビス
(4-ヒドロキシフェニル)シクロドデカン;1,1-ビス
(3,5-ジメチル-4- ヒドロキシフェニル)シクロドデカ
ン;4,4-ジヒドロキシジフェニルエーテル;4,4-チオジ
フェノール;4,4-ジヒドロキシ-3,3- ジクロロジフェニ
ルエーテル;および4,4-ジヒドロキシ-2,5- ジヒドロキ
シジフェニルエーテル等が挙げられる。これらを単独
で、または組み合わせて使用できる。また、この他に、
3以上のフェノール性水酸基を有する化合物を使用する
ことも可能である。
The (C) polycarbonate resin used in the present invention is an aromatic polycarbonate produced by a known phosgene method or a melting method (for example, JP-A-63-2).
15763 and JP-A-2-124934). The polycarbonate resin is composed of a carbonate component and a diphenol component. Examples of the precursor for introducing the carbonate component include phosgene and diphenyl carbonate. Suitable diphenols include, for example, 2,2-bis (4-hydroxyphenyl) propane (so-called bisphenol A); 2,2-bis (3,5-
Dibromo-4-hydroxyphenyl) propane; 2,2-bis (3,5-dimethyl-4-hydroxyphenyl) propane; 1,
1-bis (4-hydroxyphenyl) cyclohexane; 1,1-
Bis (3,5-dimethyl-4-hydroxyphenyl) cyclohexane; 1,1-bis (4-hydroxyphenyl) decane; 1,
4-bis (4-hydroxyphenyl) propane; 1,1-bis (4-hydroxyphenyl) cyclododecane; 1,1-bis (3,5-dimethyl-4-hydroxyphenyl) cyclododecane; 4,4-dihydroxy And diphenyl ether; 4,4-thiodiphenol; 4,4-dihydroxy-3,3-dichlorodiphenyl ether; and 4,4-dihydroxy-2,5-dihydroxydiphenyl ether. These can be used alone or in combination. In addition to this,
It is also possible to use compounds having 3 or more phenolic hydroxyl groups.

【0019】なお、ポリカーボネート系樹脂には、コポ
リエステルカーボネートのような、他の特性基を持った
ポリカーボネートや共重合体等も包含される。
The polycarbonate resin also includes polycarbonates and copolymers having other characteristic groups such as copolyestercarbonate.

【0020】成分(C)は、(A)および(B)の合計
100重量部に対して3〜50重量部、好ましくは5〜
30重量部配合される。(C)が3重量部未満の場合に
は、各樹脂の分散性の改良効果が小さく、層状剥離を生
じやすくなり、また50重量部を超えるとPEI自体の
優れた特性である耐熱性、剛性が低下してしまう。
The component (C) is 3 to 50 parts by weight, preferably 5 to 5 parts by weight based on 100 parts by weight of the total of (A) and (B).
30 parts by weight are blended. When the amount of (C) is less than 3 parts by weight, the effect of improving the dispersibility of each resin is small and delamination is likely to occur, and when it exceeds 50 parts by weight, PEI itself has excellent properties such as heat resistance and rigidity. Will decrease.

【0021】また、本発明の樹脂組成物には、その物性
を損なわない限りにおいて、その目的に応じて樹脂の混
合時、成形時に、他の樹脂、各種ゴム、慣用の添加剤、
例えば顔料、染料、補強剤(ガラス繊維、炭素繊維、チ
タン酸カリウム繊維など)、充填剤(カ―ボンブラッ
ク、シリカ、酸化チタンなど)、耐熱剤、酸化劣化防止
剤、耐候剤、滑剤、離型剤、結晶核剤、可塑剤、帯電防
止剤等を添加することができる。
In the resin composition of the present invention, other resins, various rubbers, conventional additives, etc. may be added according to the purpose at the time of mixing the resins and molding, as long as the physical properties are not impaired.
For example, pigments, dyes, reinforcing agents (glass fiber, carbon fiber, potassium titanate fiber, etc.), fillers (carbon black, silica, titanium oxide, etc.), heat-resistant agents, oxidative deterioration inhibitors, weathering agents, lubricants, release agents. A mold agent, a crystal nucleating agent, a plasticizer, an antistatic agent, etc. can be added.

【0022】本発明の樹脂組成物を製造するための方法
に特に制限はなく、通常の方法が満足に使用できる。し
かしながら一般に溶融混練法が望ましい。少量の溶剤の
使用も可能であるが、一般に必要ない。装置としては特
に押出機、バンバリ―ミキサ―、ロ―ラ―、ニ―ダ―等
を例として挙げることができ、これらを回分的または連
続的に運転する。成分の混合順は特に限定されない。
There is no particular limitation on the method for producing the resin composition of the present invention, and ordinary methods can be satisfactorily used. However, the melt-kneading method is generally preferable. The use of small amounts of solvent is possible, but generally not required. Examples of the apparatus include extruders, Banbury mixers, rollers, and kneaders, which are operated batchwise or continuously. The order of mixing the components is not particularly limited.

【0023】[0023]

【実施例】以下、実施例により本発明をさらに詳しく説
明するが、本発明はこれらに限定されるものではない。
The present invention will be described in more detail with reference to the following examples, but the present invention is not limited thereto.

【0024】なお、実施例においては次の化合物を使用
した。 成分(A) PEI:ULTEM 1010(商標、ゼネラルエレク
トリック社製) 成分(B) サーモトロピック液晶ポリエステル(LCP):p−ヒ
ドロキシ安息香酸、テレフタル酸およびエチレングリコ
ールよりなる液晶ポリエステル、ロッドランLC−5000
(商標、ユニチカ株式会社製) 成分(C) PC:ビスフェノールAのポリカーボネート、商標 LE
XAN 131 (ゼネラルエレクトリック社製)実施例1〜2および比較例1〜3 表1に示す量(重量部)の各成分を、二軸押出機(スク
リュー径30mm)を用いて、バレル設定温度320℃、回
転数300rpm で押出し、ペレットを作った。このペレ
ットから各種物性測定用の試験片を射出成形し、以下の
試験に供した。
The following compounds were used in the examples. Component (A) PEI: ULTEM 1010 (trademark, manufactured by General Electric Company) Component (B) Thermotropic liquid crystal polyester (LCP): Liquid crystal polyester composed of p-hydroxybenzoic acid, terephthalic acid and ethylene glycol, Rodran LC-5000.
(Trademark, manufactured by Unitika Ltd.) Component (C) PC: Polycarbonate of bisphenol A, trademark LE
XAN 131 (manufactured by General Electric Co.) Examples 1-2 and Comparative Examples 1-3 Each component in the amounts (parts by weight) shown in Table 1 was heated at a barrel setting temperature of 320 using a twin-screw extruder (screw diameter of 30 mm). Extrusion was carried out at a temperature of 300 rpm and a pellet was prepared. Test pieces for measuring various physical properties were injection-molded from the pellets and subjected to the following tests.

【0025】メルトインデックス(MI):ASTM
D1238に従い、300℃、6.7kg荷重で測定 アイゾット衝撃強度:ASTM D256に従い、ノッ
チ付アイゾット衝撃強度を測定 熱変形温度(HDT):ASTM D648に従い、1
8.6 kg/cm2 荷重で測定 引張り強度:ASTM D638に従って測定 層状剥離:引張り試験片を折り曲げて、目視にて判定
Melt Index (MI): ASTM
Measured according to D1238 at 300 ° C and 6.7 kg load Izod impact strength: Measured notched Izod impact strength according to ASTM D256 Heat distortion temperature (HDT): According to ASTM D648 1
Measured with 8.6 kg / cm 2 load Tensile strength: Measured according to ASTM D638 Delamination: Tensile test piece is bent and visually determined

【0026】[0026]

【表1】 [Table 1]

【0027】[0027]

【発明の効果】本発明により、溶融流動性が改善され、
しかも機械的特性の低下がなく、また層状剥離のない、
PEI系樹脂組成物が得られる。よって本発明の樹脂組
成物は広い分野で使用でき、工業的に非常に有用であ
る。
According to the present invention, the melt fluidity is improved,
Moreover, there is no deterioration in mechanical properties and there is no delamination.
A PEI resin composition is obtained. Therefore, the resin composition of the present invention can be used in a wide variety of fields and is industrially very useful.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (A)ポリエーテルイミド系樹脂 60
〜99重量部および(B)サーモトロピック液晶ポリエ
ステル 1〜40重量部を含み、さらに(A)および
(B)の合計100重量部に対して(C)ポリカーボネ
ート系樹脂 3〜50重量部を含む樹脂組成物。
1. (A) Polyetherimide resin 60
To 99 parts by weight and (B) thermotropic liquid crystal polyester 1 to 40 parts by weight, and further, (C) a polycarbonate resin 3 to 50 parts by weight based on 100 parts by weight of the total of (A) and (B). Composition.
JP35618291A 1991-12-24 1991-12-24 Resin composition containing liquid crystal polyester Pending JPH05171040A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP35618291A JPH05171040A (en) 1991-12-24 1991-12-24 Resin composition containing liquid crystal polyester

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP35618291A JPH05171040A (en) 1991-12-24 1991-12-24 Resin composition containing liquid crystal polyester

Publications (1)

Publication Number Publication Date
JPH05171040A true JPH05171040A (en) 1993-07-09

Family

ID=18447744

Family Applications (1)

Application Number Title Priority Date Filing Date
JP35618291A Pending JPH05171040A (en) 1991-12-24 1991-12-24 Resin composition containing liquid crystal polyester

Country Status (1)

Country Link
JP (1) JPH05171040A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116262855A (en) * 2022-12-22 2023-06-16 乌镇实验室 PEI (polyethylene terephthalate) casting film with high energy storage density and high flatness and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116262855A (en) * 2022-12-22 2023-06-16 乌镇实验室 PEI (polyethylene terephthalate) casting film with high energy storage density and high flatness and preparation method thereof
CN116262855B (en) * 2022-12-22 2024-02-20 乌镇实验室 PEI (polyethylene terephthalate) casting film with high energy storage density and high flatness and preparation method thereof

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