JPS62131056A - Polycarbonate resin composition - Google Patents

Polycarbonate resin composition

Info

Publication number
JPS62131056A
JPS62131056A JP27137285A JP27137285A JPS62131056A JP S62131056 A JPS62131056 A JP S62131056A JP 27137285 A JP27137285 A JP 27137285A JP 27137285 A JP27137285 A JP 27137285A JP S62131056 A JPS62131056 A JP S62131056A
Authority
JP
Japan
Prior art keywords
polycarbonate resin
resin composition
acrylic resin
weight
present
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
JP27137285A
Other languages
Japanese (ja)
Other versions
JPH0434573B2 (en
Inventor
Shigeru Nishiyama
茂 西山
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.)
Idemitsu Petrochemical Co Ltd
Original Assignee
Idemitsu Petrochemical 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 Idemitsu Petrochemical Co Ltd filed Critical Idemitsu Petrochemical Co Ltd
Priority to JP27137285A priority Critical patent/JPS62131056A/en
Publication of JPS62131056A publication Critical patent/JPS62131056A/en
Publication of JPH0434573B2 publication Critical patent/JPH0434573B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled compsn. which has excellent moldability and gives moldings having excellent surface hardness, transparency, mechanical characteristics and weather resistance, consisting of a polycarbonate resin and an acrylic resin. CONSTITUTION:70-98wt% polycarbonate resin having a structural unit of formula I (wherein Z is a single bond, a 1-8C alkylene, a 2-8C alkylidene, a 5-15C cycloalkylene, a 5-15C cycloalkylidene, SO2, SO, O, CO, a group of formula II; R is H, Cl Br, a 1-8C satd. alkyl; m is 0-4) is blended with 30-2wt% acrylic resin having a number-average MW of 1,000-10,000 [e.g., methyl (meth)acrylate] and optionally a phosphate or phosphite antioxidant, an ultraviolet absorber and other additives. The mixture is kneaded.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はポリカーボネート樹脂組成物に関し、詳しくは
表面硬度に優れ、かつ成形性に優れたポリカーボネート
樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a polycarbonate resin composition, and more particularly to a polycarbonate resin composition that has excellent surface hardness and moldability.

〔従晶術及び発明が解決しようとする問題点〕近年、自
動車、家電等の分野では省エネルギーの観点から軽量化
が行なわれており、それに伴いガラスをプラスチックで
代替することが促進されている。このようなガラス代替
品としては、透明性1機械的特性2寸法安定性に優れて
いるという理由から、ポリカーボネート樹脂成形品が有
望視されている。しかしながら、このポリカーボネート
樹脂成形品は一般に表面硬度に欠けているという問題点
があった。したがって、外観保護の観点から使用するポ
リカーボネート樹脂成形品の表面を硬化させ、耐擦過性
等を向上させることが必要となる。
[Problems to be solved by the conformal crystal technique and the invention] In recent years, in the fields of automobiles, home appliances, etc., weight reduction has been carried out from the viewpoint of energy conservation, and as a result, the replacement of glass with plastic has been promoted. Polycarbonate resin molded products are considered promising as such glass substitutes because they are excellent in transparency, mechanical properties, and dimensional stability. However, this polycarbonate resin molded article generally has a problem in that it lacks surface hardness. Therefore, from the viewpoint of protecting the appearance, it is necessary to harden the surface of the polycarbonate resin molded product used to improve scratch resistance and the like.

ポリカーボネート樹脂成形品の表面を硬化させる方法と
しては、各種のハードコート剤を塗布する方法や改質剤
をブレンドする方法が知られている。しかしながら、前
者ではポリカーボネート樹脂成形品に満足すべき表面硬
度を与えるハードコート剤が得られていないこと、成形
品の形状によっては表面処理が困難になること、該ハー
ドコート剤を塗布する工程が加わるため生産性に劣るこ
となどの問題点がある。一方、後者は簡便な方法である
が、充分な表面硬度を有する組成物は得られていない。
As methods for hardening the surface of polycarbonate resin molded articles, methods of applying various hard coating agents and methods of blending modifiers are known. However, in the former case, a hard coating agent that gives satisfactory surface hardness to polycarbonate resin molded products is not available, surface treatment becomes difficult depending on the shape of the molded product, and the process of applying the hard coating agent is added. Therefore, there are problems such as poor productivity. On the other hand, although the latter is a simple method, a composition having sufficient surface hardness has not been obtained.

したがって、本発明はポリカーボネート樹脂本来の特性
である優れた透明性や機械的性質を維持しつつ、表面硬
度、成形性等と向上せしめたポリカーボネート樹脂組成
物を提供するものである。
Therefore, the present invention provides a polycarbonate resin composition that maintains the excellent transparency and mechanical properties inherent to polycarbonate resin, while improving surface hardness, moldability, etc.

た結果、特定のアクリル樹脂を特定の割合でポリカーボ
ネート樹脂に配合した樹脂組成物が極めて優れた特性を
有していることを見出し、本発明を完成した。
As a result, they discovered that a resin composition in which a specific acrylic resin was blended with a polycarbonate resin in a specific ratio had extremely excellent properties, and the present invention was completed.

すなわち本発明は、ポリカーボネート樹脂70〜98重
量%および数平均分子量1.000〜10.000のア
クリル樹脂30〜2重量%からなるポリカーボネート樹
脂組成物を提供するものである。
That is, the present invention provides a polycarbonate resin composition comprising 70 to 98% by weight of a polycarbonate resin and 30 to 2% by weight of an acrylic resin having a number average molecular weight of 1.000 to 10.000.

本発明で用いるポリカーボネート樹脂は下記一般式 %式%() (ここで、2は結合または炭素数1〜8のアルキレン、
炭素数2〜8のアルキリデン、炭素数5〜15のシクロ
アルキレン、炭素数5〜15のシクロアルキリデン、S
O□、so、o、coまたは基を意味し、Rは水素、塩
素もしくは臭素原子または1〜8個の炭素原子を有する
飽和アルキル基を意味し、mはθ〜4の数を示す。) で表わされる構造単位を有する重合体である。
The polycarbonate resin used in the present invention has the following general formula % formula % () (where 2 is a bond or an alkylene having 1 to 8 carbon atoms,
Alkylidene having 2 to 8 carbon atoms, cycloalkylene having 5 to 15 carbon atoms, cycloalkylidene having 5 to 15 carbon atoms, S
O□, so, o, co or a group, R means a hydrogen, chlorine or bromine atom or a saturated alkyl group having 1 to 8 carbon atoms, and m represents a number of θ to 4. ) It is a polymer having a structural unit represented by:

このポリカーボネート樹脂は溶剤法、すなわち塩化メチ
レン等の溶剤中で公知の酸受容体1分子量i調整剤の存
在下、二価フェノールとホスゲンのようなカーボネート
前駆体との反応または二価フェノールとジフェニルカー
ボネートのようなカーボネート前駆体とのエステル交換
反応によって製造することができる。
This polycarbonate resin is prepared by a solvent process, i.e. by the reaction of a dihydric phenol with a carbonate precursor such as phosgene or by the reaction of a dihydric phenol with a carbonate precursor such as phosgene in the presence of a known acid acceptor molecular weight regulator in a solvent such as methylene chloride. It can be produced by transesterification reaction with carbonate precursors such as.

ここで、好適に使用し得る二価フェノールとしてはビス
フェノール類があり、特に2.2−ビス(4−ヒドロキ
シフェニル)プロパン(ビスフェノールA)が好ましい
。また、ビスフェノールAの一部または全部を他の二価
フェノールで置換したものであってもよい。ビスフェノ
ールA以外の二価フェノールとしては、例えばハイドロ
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)シクロアルカン、ビス(4−ヒドロキシフ
ェニル)スルフィド、ビス(4−ヒドロキシフェニル)
スルホン、ビス(4−ヒドロキシフェニル)スルホキシ
ド、ビス(4−ヒドロキシフェニル)エーテルのような
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、ビス(3,5−ジクロロ−4−ヒ
ドロキシフェニル)プロパンのようなハロゲン化ヒスフ
ェノール類をあげることができる。これら二価フェノー
ルは二価フェノールのホモポリマーまたは2種以上のコ
ポリマー若しくはブレンド物であってもよい。更に、本
発明で用いるポリカーボネート樹脂は多官能性芳香族化
合物を二価フェノールおよび/またはカーボネート前駆
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。
Here, dihydric phenols that can be suitably used include bisphenols, and 2,2-bis(4-hydroxyphenyl)propane (bisphenol A) is particularly preferred. Further, part or all of bisphenol A may be substituted with other dihydric phenol. Examples of dihydric phenols other than bisphenol A include hydroquinone, 4.4'-dihydroxydiphenyl, bis(4
-hydroxyphenyl)alkane, bis(4-hydroxyphenyl)cycloalkane, bis(4-hydroxyphenyl)sulfide, bis(4-hydroxyphenyl)
Compounds such as sulfone, bis(4-hydroxyphenyl) sulfoxide, bis(4-hydroxyphenyl) ether or bis(3,5-dibromo-4-hydroxyphenyl)propane, bis(3,5-dichloro-4-hydroxy Examples include halogenated hisphenols such as (phenyl)propane. These dihydric phenols may be homopolymers or copolymers or blends of two or more dihydric phenols. Furthermore, the polycarbonate resin used in the present invention may be a thermoplastic randomly branched polycarbonate obtained by reacting a polyfunctional aromatic compound with a dihydric phenol and/or a carbonate precursor.

本発明に用いるポリカーボネート樹脂は、機械的強度お
よび成形性の点からして、その粘度平均分子量は10,
000〜100,000のものが好ましく、特に20,
000〜40.000のものが好適である。
In terms of mechanical strength and moldability, the polycarbonate resin used in the present invention has a viscosity average molecular weight of 10,
000 to 100,000 is preferable, especially 20,
000 to 40.000 is suitable.

上記ポリカーボネート樹脂の配合割合は組成物全量の7
0〜98重量%、好ましくは75〜95重量%とする。
The blending ratio of the above polycarbonate resin is 7% of the total amount of the composition.
The content is 0 to 98% by weight, preferably 75 to 95% by weight.

本発明の樹脂組成物は、上記したポリカーボネート樹脂
に特定のアクリル樹脂を30〜2重量%、好ましくは2
5〜5重量%配合して構成される。
The resin composition of the present invention contains 30 to 2% by weight, preferably 2% by weight, of a specific acrylic resin in the above-mentioned polycarbonate resin.
It is composed of 5 to 5% by weight.

このアクリル樹脂の配合量が2重量%未満であると、樹
脂組成物の表面硬度が向上できず、また30重量%を超
えると、樹脂組成物の透明性が低下するので適当ではな
い。
If the amount of the acrylic resin is less than 2% by weight, the surface hardness of the resin composition cannot be improved, and if it exceeds 30% by weight, the transparency of the resin composition will decrease, which is not appropriate.

ここで用いるアクリル樹脂としては通常はアクリル酸エ
ステルまたはメタクリル酸エステルのホモポリマーまた
は2種以上のコポリマー若しくはブレンド物である。こ
のアクリル樹脂は、例えばアクリル酸メチル、アクリル
酸エチル、アクリル酸ブチル等のアクリル酸エステルや
メタクリル酸メチル、メタクリル酸エチル、メタクリル
酸ブチル、メタクリル酸シクロヘキシル等のメタクリル
酸エステルを懸濁重合、乳化重合等により重合させて製
造することができる。これらのアクリル樹脂は、数平均
分子量が1,000〜10,000、好ましくは2. 
OOO〜8. OOOの範囲のものでなければならない
。この分子量が1.000未満であると、樹脂組成物の
表面硬度向上効果が小さくなり、10.000を超える
と、樹脂組成物の透明性が低下するため適当ではない。
The acrylic resin used here is usually a homopolymer of acrylic ester or methacrylic ester, or a copolymer or blend of two or more of them. This acrylic resin is produced by suspension polymerization or emulsion polymerization of acrylic esters such as methyl acrylate, ethyl acrylate, and butyl acrylate, and methacrylic esters such as methyl methacrylate, ethyl methacrylate, butyl methacrylate, and cyclohexyl methacrylate. It can be produced by polymerization by et al. These acrylic resins have a number average molecular weight of 1,000 to 10,000, preferably 2.
OOO~8. Must be in the OOO range. If this molecular weight is less than 1.000, the effect of improving the surface hardness of the resin composition will be reduced, and if it exceeds 10.000, the transparency of the resin composition will decrease, which is not appropriate.

なお、本発明に用いるアクリル樹脂として最も好ましい
のは数平均分子量が2.000〜8. O00のポリメ
チルメタクリレート樹脂(以下、PMMA樹脂と略記す
るごとがある。)である。
The most preferable acrylic resin used in the present invention has a number average molecular weight of 2.000 to 8.00. O00 polymethyl methacrylate resin (hereinafter sometimes abbreviated as PMMA resin).

本発明のポリカーボネート樹脂組成物には、本発明の目
的を阻害しない限り、必要に応じて各種の添加剤を配合
することができる。たとえば亜すン酸エステル系、リン
酸エステル系の酸化防止剤やベンゾトリアゾール系、ベ
ンゾフェノン系の紫外線吸収剤、その他常用の種々の添
加剤を配合することができる。
The polycarbonate resin composition of the present invention may contain various additives as necessary, as long as they do not impede the purpose of the present invention. For example, sulfite-based and phosphate-based antioxidants, benzotriazole-based and benzophenone-based ultraviolet absorbers, and various other commonly used additives can be blended.

本発明のポリカーボネート樹脂組成物は上記の各成分を
配合し、混練することにより得ることができる。配合、
混練は通常の方法を採用することができ、たとえばリボ
ンブレンダ、ヘンシェルミキサー、バンバリーミキサ−
、ドラムタンブラ−2車軸スクリユ一押出機、2軸スク
リュー押出機。
The polycarbonate resin composition of the present invention can be obtained by blending and kneading the above-mentioned components. combination,
The kneading can be done using conventional methods, such as a ribbon blender, Henschel mixer, or Banbury mixer.
, drum tumbler-two-axle screw extruder, twin-screw extruder.

コニーダ、多軸スクリュー押出機等により行なうことが
できる。混練に際しての加熱温度は通常250〜300
℃が適当である。
This can be carried out using a co-kneader, multi-screw extruder, or the like. The heating temperature during kneading is usually 250 to 300
°C is appropriate.

かくして得られたポリカーボネート樹脂組成物は既知の
種々の成形方法、たとえば射出成形、押出成形、圧縮成
形、カレンダー成形1回転成形等を適用して自動車用ラ
ンプカバーなど自動車分野の成形品や家電分野等の成形
品を製造することができる。
The polycarbonate resin composition thus obtained can be molded using various known molding methods, such as injection molding, extrusion molding, compression molding, single-turn calendar molding, etc., to molded products in the automotive field such as automobile lamp covers, home appliance fields, etc. molded products can be manufactured.

なお、本発明の樹脂組成物は成形後に、シリコーン系硬
化剤等を用いてハードコートする方法を併用することが
できる。
The resin composition of the present invention may be hard-coated with a silicone curing agent or the like after being molded.

〔発明の効果〕〔Effect of the invention〕

叙上の如き本発明のポリカーボネート樹脂組成物は従来
に比べて表面硬度が向上されており、しかもポリカーボ
ネート樹脂本来の優れた透明性。
The polycarbonate resin composition of the present invention as described above has improved surface hardness compared to conventional ones, and also has the excellent transparency inherent to polycarbonate resin.

機械的特性が維持されている。さらに、流れ値(JIS
  K6719)で示される流動性に優れているため、
成形のしやすいものであり、耐候性にも優れている。
Mechanical properties are maintained. Furthermore, the flow value (JIS
K6719) has excellent fluidity,
It is easy to mold and has excellent weather resistance.

したがって、本発明のポリカーボネート樹脂組成物はガ
ラスの代替品として各種分野で有用である。
Therefore, the polycarbonate resin composition of the present invention is useful as a substitute for glass in various fields.

〔実施例〕〔Example〕

次に、本発明を実施例により詳しく説明する。 Next, the present invention will be explained in detail with reference to examples.

実施例1〜6および比較例1〜4 粘度平均分子量24.500のポリカーボネート樹脂(
出光石油化学(株製、「出光ポリカーボネート A−2
500J)および第1表に示す数平均分子量i(Mn)
のポリメチルメタクリレート樹脂をそれぞ第1表に示す
割合で結合混練し、射出成形して試験片を作成した。こ
の試験片について物性を測定した。結果を第1表に示す
。なお、表中のPC樹脂はポリカーボネート樹脂を示し
ている。
Examples 1 to 6 and Comparative Examples 1 to 4 Polycarbonate resin with a viscosity average molecular weight of 24.500 (
Idemitsu Petrochemical Co., Ltd., “Idemitsu Polycarbonate A-2
500J) and number average molecular weight i (Mn) shown in Table 1.
Polymethyl methacrylate resins were combined and kneaded in the proportions shown in Table 1, and injection molded to prepare test pieces. The physical properties of this test piece were measured. The results are shown in Table 1. Note that the PC resin in the table indicates polycarbonate resin.

Claims (3)

【特許請求の範囲】[Claims] (1)ポリカーボネート樹脂70〜98重量%および数
平均分子量1,000〜10,000のアクリル樹脂3
0〜2重量%からなるポリカーボネート樹脂組成物。
(1) Polycarbonate resin 70-98% by weight and acrylic resin 3 with number average molecular weight 1,000-10,000
A polycarbonate resin composition consisting of 0 to 2% by weight.
(2)アクリル樹脂の数平均分子量が2,000〜8,
000である特許請求の範囲第1項記載の組成物。
(2) The number average molecular weight of the acrylic resin is 2,000 to 8,
000. The composition according to claim 1, wherein the composition is:
(3)アクリル樹脂がポリメチルメタクリレートである
特許請求の範囲第1項記載の組成物。
(3) The composition according to claim 1, wherein the acrylic resin is polymethyl methacrylate.
JP27137285A 1985-12-04 1985-12-04 Polycarbonate resin composition Granted JPS62131056A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27137285A JPS62131056A (en) 1985-12-04 1985-12-04 Polycarbonate resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27137285A JPS62131056A (en) 1985-12-04 1985-12-04 Polycarbonate resin composition

Publications (2)

Publication Number Publication Date
JPS62131056A true JPS62131056A (en) 1987-06-13
JPH0434573B2 JPH0434573B2 (en) 1992-06-08

Family

ID=17499150

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27137285A Granted JPS62131056A (en) 1985-12-04 1985-12-04 Polycarbonate resin composition

Country Status (1)

Country Link
JP (1) JPS62131056A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6111016A (en) * 1997-07-23 2000-08-29 Daicel Chemical Industries, Ltd. Polycarbonate with epoxidized block copolymer
JP2008045141A (en) * 2007-10-22 2008-02-28 Idemitsu Kosan Co Ltd Polycarbonate resin composition and light guiding plate
JP2011052236A (en) * 2010-12-17 2011-03-17 Mitsubishi Rayon Co Ltd Hard-coated article
WO2015053145A1 (en) 2013-10-07 2015-04-16 三菱瓦斯化学株式会社 (meth)acrylic copolymer, resin composition, and molded product of said resin composition
KR20160138314A (en) 2015-02-05 2016-12-02 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 Polycarbonate resin composition and article molded therefrom
KR20170036663A (en) 2014-10-10 2017-04-03 아사히 가세이 케미칼즈 가부시키가이샤 Thermoplastic resin compositions, method for producing the same and molded body
KR20170100051A (en) 2015-03-30 2017-09-01 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 Resin composition and molded article using the same
KR20190055803A (en) 2016-09-26 2019-05-23 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 (Meth) acrylic copolymer, a resin composition, a molded article thereof, and a method for producing a molded article
CN111518378A (en) * 2020-04-19 2020-08-11 东莞市骄阳塑胶科技有限公司 Special transparent high-surface-hardness wear-resistant polycarbonate material and preparation method thereof

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6510188B2 (en) * 2014-06-10 2019-05-08 帝人株式会社 Resin composition

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4880650A (en) * 1972-01-03 1973-10-29
JPS4886955A (en) * 1972-01-24 1973-11-16
JPS538732A (en) * 1976-07-12 1978-01-26 Toa Nenryo Kogyo Kk Method of producing separator for battery
JPS5628937A (en) * 1979-08-11 1981-03-23 Seikou Kogyo Kk Multishaft excavator

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4880650A (en) * 1972-01-03 1973-10-29
JPS4886955A (en) * 1972-01-24 1973-11-16
JPS538732A (en) * 1976-07-12 1978-01-26 Toa Nenryo Kogyo Kk Method of producing separator for battery
JPS5628937A (en) * 1979-08-11 1981-03-23 Seikou Kogyo Kk Multishaft excavator

Cited By (16)

* Cited by examiner, † Cited by third party
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