JPS60250060A - Polycarbonate resin composition - Google Patents

Polycarbonate resin composition

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Publication number
JPS60250060A
JPS60250060A JP10636084A JP10636084A JPS60250060A JP S60250060 A JPS60250060 A JP S60250060A JP 10636084 A JP10636084 A JP 10636084A JP 10636084 A JP10636084 A JP 10636084A JP S60250060 A JPS60250060 A JP S60250060A
Authority
JP
Japan
Prior art keywords
polycarbonate resin
resistance
resin composition
resin
impact
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.)
Granted
Application number
JP10636084A
Other languages
Japanese (ja)
Other versions
JPH0117502B2 (en
Inventor
Osamu Ohara
大原 治
Kazuo Kishimoto
岸本 一男
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.)
Teijin Ltd
Original Assignee
Teijin Chemicals 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 Teijin Chemicals Ltd filed Critical Teijin Chemicals Ltd
Priority to JP10636084A priority Critical patent/JPS60250060A/en
Publication of JPS60250060A publication Critical patent/JPS60250060A/en
Publication of JPH0117502B2 publication Critical patent/JPH0117502B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To provide the titled resin compsn. having improved moldability, resistance to solvents and low-temperature impact, by blending a polycarbonate resin, an ABS resin and butyl rubber in a specified ratio. CONSTITUTION:20-200pts.wt. acrylonitrile/butadiene/styrene copolymer resin (e.g. ABS-10, a product of Nippon Gosei Gomu K.K.) and 0.5-7pts.wt. butyl rubber (e.g. IIR-065, a product of Nippon Gosei Gomu K.K.) are mixed with 100pts. wt. polycarbonate resin (e.g. Panlite L-1225, a product of Teijin Kasei K.K.). The mixture is melt-kneaded in an extruder or a kneader to obtain the desired polycarbonate resin compsn.

Description

【発明の詳細な説明】 本発明はポリカーボネート樹脂組成物に係わり、詳しく
は耐溶剤性、低温における耐衝撃性と成形性の改良され
たポリカーボネート樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polycarbonate resin composition, and more particularly to a polycarbonate resin composition with improved solvent resistance, impact resistance at low temperatures, and moldability.

従来技術 ポリカーボネート樹脂は高度の耐衡撃性を具備し、自己
消火性であり、耐熱性が他の樹脂に比して高り、シかも
電気的特性及び寸法安定性が優れていることから、エン
ジニアリングプラスチックとして広く知られている。
Conventional technology Polycarbonate resin has a high degree of shock resistance, is self-extinguishing, has higher heat resistance than other resins, and has excellent electrical properties and dimensional stability. It is widely known as an engineering plastic.

また、ポリカーボネート樹脂の成形性と衝撃強度の厚み
依存性毫改良したポリカーボネート樹脂とABS樹脂(
アクリ、−ニトリル−ジエン系ゴム−スチレン重合体の
略)との混合物(’I公昭38−15225号公報、特
公昭39−71号公報、4I公昭42−11496号公
報、特開1848−43750号公報、41開昭53−
7757号公報、特開昭53− 130749号公報)もよく知られている。
In addition, the thickness dependence of polycarbonate resin moldability and impact strength was improved using polycarbonate resin and ABS resin (
Acrylic, -nitrile-diene rubber-styrene polymer mixture) Official Gazette, 41 Kaisho 53-
7757, Japanese Patent Application Laid-Open No. 130749/1983) are also well known.

自動車のバンパー、パネル、スポイラ−。Automobile bumpers, panels, and spoilers.

ドアーハンドル等の外装部品は従来スチールで作られて
きたが、昨今の低燃費化、軽量化に伴なってプラスチッ
ク化への要望が強くなってきている。また、スチールに
比べて耐腐食性やへり込み難いといったプラスチックの
利A カ見直されている。
Exterior parts such as door handles have traditionally been made of steel, but with recent advances in fuel efficiency and weight reduction, there is a growing demand for plastics. Additionally, the advantages of plastic, such as its corrosion resistance and resistance to denting, are being reconsidered compared to steel.

該自動車部品に使用されるプラスチックとしては、耐衝
撃性、耐熱性、成形性かつ上記のポリカーボネート樹脂
とABS樹脂の混合物が注目されている。しかしながら
、ポリカーボネートa脂−ABS樹脂混合物は自動車部
品等に使用する上で、耐溶剤性が低いことが大きな問題
となっている。該欠点を改良する方法として、上記混合
物にポリアミド樹脂を添加する方法が特開昭56−18
647号公報に開示されている。しかし、この方法では
耐溶剤性は向上するが満足できるものでな(、さらに衝
撃強度がと(K低温で低下する欠点がある。
As plastics used for such automobile parts, attention has been focused on impact resistance, heat resistance, moldability, and mixtures of the above-mentioned polycarbonate resins and ABS resins. However, when polycarbonate a resin-ABS resin mixtures are used for automobile parts and the like, their low solvent resistance is a major problem. As a method to improve this drawback, a method of adding a polyamide resin to the above mixture is disclosed in Japanese Patent Application Laid-Open No. 56-18.
It is disclosed in Japanese Patent No. 647. However, although this method improves solvent resistance, it is not satisfactory (and also has the disadvantage that impact strength decreases at low temperatures).

発明の目的 本発明の目的はハイオクタンガソリン等の溶剤に対する
抵抗性、1/4インチのフイゾット衝撃強さ、低温での
衝撃強さおよび成形性の改良されたポリカーボネート樹
脂組成物を提供することKある。
OBJECTS OF THE INVENTION An object of the present invention is to provide a polycarbonate resin composition having improved resistance to solvents such as high octane gasoline, 1/4 inch Fizot impact strength, low temperature impact strength and moldability. be.

発明の構成 本発明はポリカーボネート樹脂(4)100重量部、A
BS樹脂Q3)20〜200重量部およびブチルゴム0
0.5〜7重量部からなるポリカーボネート樹脂組成物
に関する。
Structure of the invention The present invention consists of 100 parts by weight of polycarbonate resin (4), A
BS resin Q3) 20 to 200 parts by weight and 0 butyl rubber
The present invention relates to a polycarbonate resin composition containing 0.5 to 7 parts by weight.

本発明に用いられるポリカーボネート樹脂(4)は、通
常酸受容体および分子量調整剤の存在下での2価フェノ
ールとホスゲン等のカーボネート前駆体との反応、或い
は2価フェノールとジフェニルカーボネート等のカーボ
ネート前駆体とのエステル交換反応によって製造される
。ここで使用しうる2価フェノールとしては、ビスフェ
ノールが好ましく、とくに2.2−ビス(4−ヒドロキ
シフェニル)プロパン(以下ビスフェノールAと称ス)
カ好ましい。
The polycarbonate resin (4) used in the present invention is usually prepared by reacting dihydric phenol with a carbonate precursor such as phosgene in the presence of an acid acceptor and a molecular weight regulator, or by reacting dihydric phenol with a carbonate precursor such as diphenyl carbonate. It is produced by transesterification reaction with As the dihydric phenol that can be used here, bisphenol is preferable, particularly 2,2-bis(4-hydroxyphenyl)propane (hereinafter referred to as bisphenol A).
It is preferable.

また、ビスフェノールAの一部または全部を他の2価フ
ェノールで置換してもよい。ビスフェノールA以外の2
価フェノールとしては、例えばハイドルキノン、4.4
’−ジヒドロキシジフェニル、ビス(4−ヒドロキシフ
ェニル)アルカン、ビス(4−ヒドロキシフェニル)ジ
クロフルカン、ビス(4−ヒドロキシフェニル)スルフ
イツト、ビス(4−ヒドロキシフェニル)スルホン、ビ
ス(4−ヒトルキシジフェニル)スルホキシド、ビス(
4−ヒドロキシフェニル)エーテルの如# 化合物また
はビス(3,5−ジブロモ−4−ヒドロキシフェニル)
プロパンの如きハロゲン化ビスフェノール類をあげるこ
とができる。
Further, part or all of bisphenol A may be replaced with other dihydric phenol. 2 other than bisphenol A
Examples of the hydric phenol include hydroquinone, 4.4
'-dihydroxydiphenyl, bis(4-hydroxyphenyl)alkane, bis(4-hydroxyphenyl)dicloflucan, bis(4-hydroxyphenyl)sulfite, bis(4-hydroxyphenyl)sulfone, bis(4-hydroxydiphenyl)sulfoxide ,Screw(
Compounds such as 4-hydroxyphenyl) ether or bis(3,5-dibromo-4-hydroxyphenyl)
Examples include halogenated bisphenols such as propane.

ポリカーボネート樹脂は、これら2価フェノールのホモ
ポリマーまたは21!以上のコポリマー或いはこれらの
ブレンド物であってもよい。またポリカーボネート樹脂
はその一部が分岐されていてもよ(、例えば多官能性芳
香族化合物と2価フェノールなカーボネート前駆体と反
応させた熱可塑性ランダム分岐ポリカーボネートであっ
てもよい。
Polycarbonate resin is a homopolymer of these dihydric phenols or 21! The above copolymers or blends thereof may be used. Further, the polycarbonate resin may be partially branched (for example, it may be a thermoplastic randomly branched polycarbonate made by reacting a polyfunctional aromatic compound with a dihydric phenol carbonate precursor).

本発11に用いられるABS@脂(6)は通常市販され
ているものでよく、その配合量はポリカーボネート樹脂
囚100重量部当り20〜200重量部であり、好まし
くは30〜170重量部である。配合量が上述の範囲よ
り少ないと本発明の樹脂組成物のような耐溶剤性。
The ABS@fat (6) used in the present invention 11 may be a commercially available one, and its blending amount is 20 to 200 parts by weight, preferably 30 to 170 parts by weight, per 100 parts by weight of the polycarbonate resin. . If the blending amount is less than the above range, the resin composition of the present invention will not have the same solvent resistance.

低温での耐衝撃性が得られず、多いとポリカーボネート
樹脂の特長である耐熱性が大巾に低下する。
Impact resistance at low temperatures cannot be obtained, and if the amount is too high, the heat resistance, which is a feature of polycarbonate resin, will be significantly reduced.

本発明に用いられるブチルゴム0は通常市販されている
ものでよく、その配合量はポリカーボネート樹脂囚10
0重量部当り0.5〜7重量部であり、好ましくは1〜
5重量部である。配合量が上述の範囲より少ないと本発
明の樹脂組成物のような耐溶剤性が得られず、多いと層
剥離が生じて成形品の外観を損う。
The butyl rubber used in the present invention may be any commercially available one, and its blending amount is 10% of the polycarbonate resin.
0.5 to 7 parts by weight, preferably 1 to 7 parts by weight
5 parts by weight. If the amount is less than the above-mentioned range, it will not be possible to obtain the solvent resistance of the resin composition of the present invention, and if it is more, layer peeling will occur and the appearance of the molded product will be impaired.

本発明のポリカーボネート樹脂組成物の調製は任意の方
法で行うことができる。例えばポリカーボネート樹脂(
6)にABS樹脂(ロ)およびブチルゴムCC)を加え
、V型ブレンダー。
The polycarbonate resin composition of the present invention can be prepared by any method. For example, polycarbonate resin (
Add ABS resin (b) and butyl rubber CC) to 6) and use a V-type blender.

スーパーミキサー等を用いて混合したのち、押出機、コ
ニーダ郷にて溶融混合する方法、(ト)と(Q成分をあ
らかじめ混a−−ル、パンツミリミキサーにて混合し、
これをポリカーボネート樹脂に溶融状態で混合する方法
などかある。
A method of mixing using a super mixer etc. and then melt-mixing using an extruder at Konida Go, a method of mixing components (G) and (Q) in advance with a mixer in a pant milli mixer,
There is a method of mixing this with polycarbonate resin in a molten state.

また、本発明の組成物にはその用途に応じてガラス繊維
の如き強化剤、熱安定剤、酸化防止剤2発泡剤、光安定
剤、難燃剤、可塑剤。
The composition of the present invention may also contain a reinforcing agent such as glass fiber, a heat stabilizer, an antioxidant, a blowing agent, a light stabilizer, a flame retardant, and a plasticizer, depending on its use.

離型剤、帯電防止剤、染料な−どを添加することができ
る。
A mold release agent, an antistatic agent, a dye, etc. can be added.

発明の効果 本発明のポリカーボネート樹脂組成物は耐溶剤性が大巾
に改良され、低温での衝撃強さオヨヒ成形性に優れてい
るので、バンパー。
Effects of the Invention The polycarbonate resin composition of the present invention has greatly improved solvent resistance, and has excellent impact strength and moldability at low temperatures, so it can be used as a bumper.

パネル、フェンター、スポイラ−、ドアーハンドル等の
自動車の外装部品に使用できる。
Can be used for automotive exterior parts such as panels, fenders, spoilers, and door handles.

実 施 例 以下に実施例を掲げて本発明をさらに説明する。なお、
耐溶剤性、耐衝撃性、低温での耐衝撃性は下記の方法で
評価した。
EXAMPLES The present invention will be further explained with reference to Examples below. In addition,
Solvent resistance, impact resistance, and impact resistance at low temperatures were evaluated using the following methods.

1、 耐溶剤性評価法 I)ガソリン中の曲げ強さ保持率 予め乾燥したペレットを射出成形機を 用いて、127鰭X 12.7 m X 6.35wx
の曲げ試験片に成形した。曲げ試験片は温度23℃、湿
度50%で24時間処理したのち、引張試験機(新興■
製; TOM500D型)Icて23℃で曲げ強さくa
)を測定した。また、曲げ試験片は温度23℃。
1. Solvent resistance evaluation method I) Bending strength retention in gasoline Using an injection molding machine, pre-dried pellets were molded into 127 fins x 12.7 m x 6.35 wx.
It was molded into a bending test piece. The bending test pieces were processed at a temperature of 23°C and a humidity of 50% for 24 hours, then tested using a tensile tester (Shinko).
made; TOM500D type) Ic bending strength a at 23℃
) was measured. In addition, the temperature of the bending test piece was 23°C.

湿度50%にて処理したのち、ガソリン(丸善石油■レ
ギュラーガソリン)中に15秒間浸し、そのまへの状態
で上記と同様にして曲げ強さくb)を測定した。耐溶剤
性は強度保持率(o)=((b)/(a))xtoo 
Kて評価した。保持率は大きい程、耐溶剤性のよいこと
を表わす。
After processing at 50% humidity, it was immersed in gasoline (Maruzen Oil Regular Gasoline) for 15 seconds, and the bending strength b) was measured in the same manner as above. Solvent resistance is strength retention rate (o) = ((b)/(a))xtoo
Rated K. The higher the retention rate, the better the solvent resistance.

II) 溶剤中での割れ発生時間 予め乾燥したペレット射出成形機を用 いて、引張試験片(ASTM D−638゜タイプエダ
ンベル)K成形した。この引張試験片は巾30譚、厚さ
1o■、長さ250關のステンレス鋼材を半径227■
に曲げた殆具に取りつけ、種々のハイオクタンガソリン
の代りのイソオクタン−トルエン1:1混合液に浸漬し
、試験片が割れるまでの時間を創った。割れ発生時間が
長い程、耐溶剤性が大きいことを表わす。
II) Crack occurrence time in solvent A tensile test piece (ASTM D-638° type dumbbell) K was molded using a pellet injection molding machine that had been dried in advance. This tensile test piece is a stainless steel material with a width of 30mm, a thickness of 1o, and a length of 250mm.
The specimens were attached to most of the bent tools and immersed in a 1:1 mixture of isooctane and toluene instead of various high-octane gasolines to create a time period until the specimens cracked. The longer the crack generation time, the greater the solvent resistance.

2、 耐衝撃性評価法 予め乾燥したベレットを射出成形機を用いて、64mm
X12.7鰭X3.18mと64■X 12.7mX 
6.35關の衝撃試験片に成形した。該試験片は0.2
5WRのノツチを付けたのち、温度23℃、湿度50%
で24時間処理した。その後フイゾット衝撃試験機(東
洋精機■製)Kて衝撃強さを測定した。衝撃強さが大き
い程、耐衝撃性のよいことを表わす。
2. Impact resistance evaluation method Using an injection molding machine, pre-dried pellets were molded into 64mm
X12.7 fins X3.18m and 64■X 12.7mX
It was molded into a 6.35 inch impact test piece. The test piece is 0.2
After attaching the 5WR notch, the temperature was 23℃ and the humidity was 50%.
It was treated for 24 hours. Thereafter, the impact strength was measured using a Fizot impact tester K (manufactured by Toyo Seiki ■). The higher the impact strength, the better the impact resistance.

3、 低温での耐衝撃性 上記2で成形したノツチ付衝撃試験片を−30℃の恒温
器中に1時間放置したのち、恒温器からとり出し、直ち
に上記2のフイゾット衝撃試験機にて衝撃強さを測定し
た。
3. Impact resistance at low temperatures The notched impact test piece formed in 2 above was left in a -30°C incubator for 1 hour, then taken out of the incubator and immediately subjected to impact testing using the Fizot impact tester in 2 above. The strength was measured.

衝撃強さが高い程、低温での耐衝撃性の優れるごとを表
わす。
The higher the impact strength, the better the impact resistance at low temperatures.

実施例1〜4及び比較例1〜3 予め乾燥したポリカーボネート樹脂(2)(帝人化帽1
パンライトL−1225)l第1表に示したABSIl
l脂およびブチルゴム(日本合成ゴム#:IIR−06
5)を第1 !! K yr、 ス量−C−VUプレン
ターを用いて混合し、ついで30翻φ押出機(中央機械
■$1!:VSK−30)で押出しペレット化した。得
られたベレットを用いて上記評価方法に示した方法で試
験片を射出成形し、その耐溶剤性、耐衝撃性、低温での
耐衝撃性を評価した。その結果を#!1表に示す。
Examples 1 to 4 and Comparative Examples 1 to 3 Pre-dried polycarbonate resin (2) (Teijinka Hat 1
Panlight L-1225) ABSI shown in Table 1
l fat and butyl rubber (Japanese Synthetic Rubber #: IIR-06
5) First! ! The mixture was mixed using a C-VU printer, and then extruded into pellets using a 30 mm extruder (Chuo Machinery ■$1!: VSK-30). Using the obtained pellet, a test piece was injection molded by the method shown in the evaluation method above, and its solvent resistance, impact resistance, and impact resistance at low temperatures were evaluated. # the result! It is shown in Table 1.

手続補正書 昭和59年 9月6日 特許庁長官殿 1、事件の表示 特願昭 59−106360 号 2、発明の名称 ポリカーボネート樹脂組成物 3、補正をする者 事件との関係 特許出願人 代表者 山 崎 芳 樹 5、補正の対象 明細書の「発明の詳細な説明」の欄 6、補正の内容 (1)明細書の第2頁最下行に「成形性力1つ上記」と
あるを「成形性から上記」に訂正する。
Procedural amendment dated September 6, 1980, Commissioner of the Japan Patent Office 1, Indication of the case, Patent Application No. 1983-106360, 2, Title of the invention: Polycarbonate resin composition 3, Person making the amendment Relationship to the case Representative of the patent applicant Yoshiki Yamazaki 5, "Detailed Description of the Invention" column 6 of the specification to be amended, contents of the amendment (1) In the bottom line of the second page of the specification, the phrase "formability strength is one or more" has been changed to " The above is corrected from the viewpoint of formability.

(2)同第5頁第3行目に[0キシジフェニル)」とあ
るをしOキシフェニル)」に訂正する。
(2) On page 5, line 3, the text "[0-oxydiphenyl)" has been corrected to "O-oxyphenyl)."

(3)同第8頁第14行目に[ペレット射出成形機]と
あるを「ベレットを射出成形機」に37正する。
(3) In the 14th line of page 8, the phrase "pellet injection molding machine" is corrected to "pellet injection molding machine".

以 上that's all

Claims (1)

【特許請求の範囲】[Claims] ポリカーボネート樹脂囚100重量部、アクリロニトリ
ルーズタジエンースチレン共重合樹脂@20〜200重
量部およびブチルゴム00.5〜7重量部からなるポリ
カーボネート樹脂組成物。
A polycarbonate resin composition consisting of 100 parts by weight of a polycarbonate resin, 20 to 200 parts by weight of an acrylonitrile loosetadiene-styrene copolymer resin, and 00.5 to 7 parts by weight of butyl rubber.
JP10636084A 1984-05-28 1984-05-28 Polycarbonate resin composition Granted JPS60250060A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10636084A JPS60250060A (en) 1984-05-28 1984-05-28 Polycarbonate resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10636084A JPS60250060A (en) 1984-05-28 1984-05-28 Polycarbonate resin composition

Publications (2)

Publication Number Publication Date
JPS60250060A true JPS60250060A (en) 1985-12-10
JPH0117502B2 JPH0117502B2 (en) 1989-03-30

Family

ID=14431574

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10636084A Granted JPS60250060A (en) 1984-05-28 1984-05-28 Polycarbonate resin composition

Country Status (1)

Country Link
JP (1) JPS60250060A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0693530A3 (en) * 1994-07-20 1996-07-17 Bayer Ag Impact modified moulding masses based on polyisobutylene-containing-polycarbonate
EP0842983A3 (en) * 1996-11-18 1998-07-29 General Electric Company Polycarbonate/ABS blends

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0693530A3 (en) * 1994-07-20 1996-07-17 Bayer Ag Impact modified moulding masses based on polyisobutylene-containing-polycarbonate
US5747586A (en) * 1994-07-20 1998-05-05 Bayer Ag High-impact molding compounds based on polyisobutylene-containing polycarbonate
EP0842983A3 (en) * 1996-11-18 1998-07-29 General Electric Company Polycarbonate/ABS blends
CN1122080C (en) * 1996-11-18 2003-09-24 通用电气公司 Polycarbonate/ABS blends
KR100514237B1 (en) * 1996-11-18 2006-01-27 제너럴 일렉트릭 캄파니 Polycarbonate/abs blends

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