JP2002012748A - Resin composition - Google Patents
Resin compositionInfo
- Publication number
- JP2002012748A JP2002012748A JP2000195439A JP2000195439A JP2002012748A JP 2002012748 A JP2002012748 A JP 2002012748A JP 2000195439 A JP2000195439 A JP 2000195439A JP 2000195439 A JP2000195439 A JP 2000195439A JP 2002012748 A JP2002012748 A JP 2002012748A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- component
- polyester resin
- pctg
- glycol
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、樹脂組成物、とく
にポリカーボネート樹脂の透明性、耐衝撃性を損なうこ
となく、流動性にも優れる樹脂組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition, and more particularly to a resin composition having excellent fluidity without impairing the transparency and impact resistance of a polycarbonate resin.
【0002】[0002]
【従来の技術および発明が解決しようとする課題】ポリ
カーボネート樹脂は、透明性、耐衝撃性に優れており、
シート、フィルム、成型品等多用途に使用されている
が、流動性が低く成形性が悪いという問題がある。2. Description of the Related Art Polycarbonate resins have excellent transparency and impact resistance.
Although it is used for various purposes such as sheets, films and molded products, it has a problem that the fluidity is low and the moldability is poor.
【0003】これを解消するため、ポリカーボネート樹
脂にポリエステル系樹脂を添加することが提案されてい
る(特公昭36−014035、特公昭58−0183
91)が、この方法ではポリカーボネート樹脂の持つ透
明性、あるいは耐衝撃性を損なうという問題があった。In order to solve this problem, it has been proposed to add a polyester resin to a polycarbonate resin (JP-B-36-014035, JP-B-58-0183).
91), however, this method has a problem in that the transparency or impact resistance of the polycarbonate resin is impaired.
【0004】本発明は、この従来技術の問題点を改善す
る事を目的とし、ポリカーボネート樹脂の透明性、耐衝
撃性を損なわずに、流動性を向上させる樹脂組成物を提
供するものである。An object of the present invention is to provide a resin composition which improves the flowability without impairing the transparency and impact resistance of a polycarbonate resin, with the object of solving the problems of the prior art.
【0005】[0005]
【課題を解決するための手段】上記目的を達成するため
に鋭意研究した結果、ポリカーボネート樹脂に、特定の
ポリエステル樹脂を配合することにより上記問題点が解
決できる、とくにこの樹脂を配合することにより、ポリ
カーボネート樹脂の透明性が損なわれるという問題点解
決への寄与が大きいということを見いだしたものであ
る。As a result of intensive studies to achieve the above object, the above problems can be solved by blending a specific polyester resin with a polycarbonate resin. In particular, by blending this resin, It has been found that the contribution to solving the problem that the transparency of the polycarbonate resin is impaired is great.
【0006】すなわち、本発明に係る樹脂組成物は、ポ
リカーボネート樹脂95〜5重量部と、ポリエステル樹
脂5〜95重量部とよりなる混合樹脂において、ポリエ
ステル樹脂の少なくとも1種類が、テレフタル酸および
テレフタル酸誘導体からなる郡より選ばれる1種または
2種以上のテレフタル酸系成分からなるジカルボン酸系
重縮合成分と、1,4−シクロヘキサンジメタノールを
40モル%以上含有するグリコール系重縮合成分とを重
縮合させて得られる下記一般式(I)That is, in the resin composition according to the present invention, in a mixed resin comprising 95 to 5 parts by weight of a polycarbonate resin and 5 to 95 parts by weight of a polyester resin, at least one of the polyester resins contains terephthalic acid and terephthalic acid. A dicarboxylic acid-based polycondensation component comprising one or more terephthalic acid-based components selected from the group consisting of derivatives and a glycol-based polycondensation component containing 1,4-cyclohexanedimethanol in an amount of 40 mol% or more. The following general formula (I) obtained by condensation
【化2】 で表される反復単位を構造中に有するポリエステル樹脂
(PCTGと呼ぶ)であり、該PCTGの重量比が全体
のポリエステル樹脂成分の10%以上であることを特徴
とするものである。Embedded image (PCTG) having a repeating unit represented by the following formula in its structure, wherein the weight ratio of the PCTG is 10% or more of the entire polyester resin component.
【0007】本発明のポリカーボネート樹脂とは、ビス
フェノール化合物から周知の方法で製造されるものが使
用可能であり、また異なるタイプのものを併用してもよ
い。As the polycarbonate resin of the present invention, those produced from a bisphenol compound by a known method can be used, and different types may be used in combination.
【0008】本発明のポリエステル樹脂とは、グリコー
ル系縮合成分とジカルボン酸系成分とを重縮合させて得
られるものであり、グリコール成分としては、エチレン
グリコール、プロプレン1,2−グリコール、プロプレ
ン1,3−グリコール、1,4−ブタジオール、2,3
−ブタジオール、ヘキサン1,6−ジオール等のグリコ
ール成分を挙げることができる。ジカルボン酸成分とし
てはイソフタル酸、テレフタル酸、オルトフタル酸、ビ
フェニルジカルボン酸などを挙げることが出来る。これ
らのグリコールとジカルボン酸をそれぞれ単独で使用し
ても良いし、2種以上のグリコールあるいはカルボン酸
を組み合わせても良い。また、得られたポリエステルを
単独で使用しても、組み合わせて使用しても良い。The polyester resin of the present invention is obtained by polycondensing a glycol-based condensation component and a dicarboxylic acid-based component. Examples of the glycol component include ethylene glycol, propylene 1,2-glycol, propylene 1,1-glycol, and the like. 3-glycol, 1,4-butadiol, 2,3
And glycol components such as butadiol and hexane 1,6-diol. Examples of the dicarboxylic acid component include isophthalic acid, terephthalic acid, orthophthalic acid, and biphenyldicarboxylic acid. These glycols and dicarboxylic acids may be used alone or in combination of two or more glycols or carboxylic acids. Further, the obtained polyesters may be used alone or in combination.
【0009】本発明において、少なくとも1種類のポリ
エステル樹脂として、前記PCTGを用いる必要があ
り、該PCTGの重量比が全体のポリエステル樹脂成分
の10%以上であるものを用いる必要がある。In the present invention, it is necessary to use the above-mentioned PCTG as at least one kind of polyester resin, and it is necessary to use a resin in which the weight ratio of the PCTG is 10% or more of the entire polyester resin component.
【0010】上記PCTGにおいて、テレフタル酸誘導
体とは、例えば、テレフタル酸ジメチル、テレフタル酸
ジエチル等が挙げられるが、中でもテレフタル酸ジメチ
ルが好適である。グリコール系縮合成分としては、1,
4−シクロヘキサンジメタノールを40モル%以上用い
る必要がある。すなわち、グリコール系縮合成分全体占
める1,4−シクロヘキサンジメタノールの割合が40
モル%未満では、透明性が得られず、40モル%以上必
要であり、50モル%以上とするのがより望ましい。な
お、1,4−シクロヘキサンジメタノールは、シス型と
トランス型の2種の異性体が存在するが、いずれであっ
ても良い。 1,4−シクロヘキサンジメタノールと併
用して用いるグリコール系縮合成分としては、例えばエ
チレングリコール、プロプレングリコールなどが挙げら
れるが、物性バランスがよく、広く工業生産され安価で
あることから、エチレングリコールが特に好適である。
もちろん、グリコール系縮合成分として1,4−シクロ
ヘキサンジメタノールを100%使用するものとして良
い。In the above-mentioned PCTG, the terephthalic acid derivative includes, for example, dimethyl terephthalate, diethyl terephthalate and the like, among which dimethyl terephthalate is preferable. As the glycol-based condensation component, 1,
It is necessary to use 40 mol% or more of 4-cyclohexanedimethanol. That is, the ratio of 1,4-cyclohexanedimethanol in the entire glycol-based condensation component is 40%.
If it is less than mol%, transparency cannot be obtained, and it is necessary to be 40 mol% or more, and it is more desirable to be 50 mol% or more. In addition, 1,4-cyclohexanedimethanol has two types of isomers, cis-type and trans-type, and any of them may be used. Examples of the glycol-based condensation component used in combination with 1,4-cyclohexanedimethanol include ethylene glycol and propylene glycol.Ethylene glycol is well-balanced in physical properties, is widely industrially produced, and is inexpensive. Particularly preferred.
Of course, 100% 1,4-cyclohexanedimethanol may be used as the glycol-based condensation component.
【0011】この発明において、ポリカーボネート樹脂
とポリエステル樹脂との混合重量比は、95/5〜5/
95の範囲とする必要があり、且つPCTGのポリエス
テル樹脂全体に占める重量比は10%以上とする必要が
ある。In the present invention, the mixing weight ratio between the polycarbonate resin and the polyester resin is from 95/5 to 5 /
95, and the weight ratio of PCTG to the entire polyester resin must be 10% or more.
【0012】ポリエステル樹脂の重量比が5%未満の場
合、ポリカーボネート樹脂の流動性が改良されない。一
方、ポリエステル樹脂の重量比が95%を越えると、ポ
リカーボネート樹脂の耐衝撃性が保たれない。When the weight ratio of the polyester resin is less than 5%, the flowability of the polycarbonate resin is not improved. On the other hand, if the weight ratio of the polyester resin exceeds 95%, the impact resistance of the polycarbonate resin cannot be maintained.
【0013】PCTGの全ポリエステル樹脂中の重量比
が10%未満の場合、本発明に係るポリカーボネート系
樹脂組成物の透明性が得られない。なお、このPCTG
が100%であってもよい。When the weight ratio of PCTG to the total polyester resin is less than 10%, the transparency of the polycarbonate resin composition according to the present invention cannot be obtained. Note that this PCTG
May be 100%.
【0014】なお、本発明の樹脂組成物には、酸化防止
剤、可塑剤、改質剤、光安定剤、紫外線吸収剤、フィラ
ー、蛍光増白剤、帯電防止剤等の各種添加剤を適宜配合
しても良い。また、本発明の樹脂組成物は、押出機、カ
レンダー、インジェクション等の成形機により容易にシ
ート、フィルム等の所望の形状にする事が出来る。The resin composition of the present invention may contain various additives such as an antioxidant, a plasticizer, a modifier, a light stabilizer, an ultraviolet absorber, a filler, a fluorescent brightener, and an antistatic agent. You may mix. Further, the resin composition of the present invention can be easily formed into a desired shape such as a sheet or a film by a molding machine such as an extruder, a calender, and an injection.
【0015】[0015]
【実施例】次に、この発明の具体的実施例について説明
する。Next, specific embodiments of the present invention will be described.
【0016】まず、実施例、比較例には次に示す原料を
使用した。 (ポリカーボネート樹脂)三菱エンジニアリングプラス
チック社製「ユーピロン E2000F」 (ポリエステル樹脂) (1)三菱レーヨン社製「PA−280」(ジカルボン
酸成分がテレフタル酸であり、グリコール成分がエチレ
ングリコールであるポリエステル樹脂) (2)東レ社製「1401」(グリコール成分が1,4
−ブタンジオールであるポリエステル樹脂) (3)セハン社製「H3212」(ジカルボン酸成分が
イソフタル酸であり、グリコール成分がエチレングリコ
ールであるポリエステル樹脂) (4)イーストマンケミカル社製「PCTG5445」
(1,4−シクロヘキサンジメタノールの割合が50モ
ル%であるポリエステル樹脂) (5)イーストマンケミカル社製「PETG1447
1」(1,4−シクロヘキサンジメタノールの割合が3
0モル%であるポリエステル樹脂)First, the following raw materials were used in Examples and Comparative Examples. (Polycarbonate resin) "Iupilon E2000F" manufactured by Mitsubishi Engineering-Plastics Corporation (polyester resin) (1) "PA-280" manufactured by Mitsubishi Rayon Co. (polyester resin whose dicarboxylic acid component is terephthalic acid and whose glycol component is ethylene glycol) ( 2) Toray “1401” (glycol component is 1,4)
-Polyester resin which is butanediol) (3) "H3212" manufactured by Sehan (polyester resin whose dicarboxylic acid component is isophthalic acid and whose glycol component is ethylene glycol) (4) "PCTG5445" manufactured by Eastman Chemical Company
(Polyester resin having a ratio of 1,4-cyclohexanedimethanol of 50 mol%) (5) "PETG147" manufactured by Eastman Chemical Company
1 "(when the ratio of 1,4-cyclohexanedimethanol is 3
0 mol% polyester resin)
【0017】<実施例1〜5、及び比較例1〜6>各樹
脂を表1に示した割合でタンブラーミキサーを使い混合
し、これを120℃オーブン中で24時間乾燥させた
後、20mm径射出成形機を用いて、1mm厚みで、5
0x100mmサイズのプレートを作製し、このものの
透明性、耐衝撃性を評価した。さらに、上記射出成形機
により流動性の評価を行った。これら評価方法は次の通
りである。<Examples 1 to 5 and Comparative Examples 1 to 6> Each resin was mixed at a ratio shown in Table 1 using a tumbler mixer, and dried in an oven at 120 ° C. for 24 hours. Using an injection molding machine, 1 mm thick and 5
A plate having a size of 0x100 mm was prepared, and its transparency and impact resistance were evaluated. Furthermore, the fluidity was evaluated by the above-mentioned injection molding machine. These evaluation methods are as follows.
【0018】透明性;JIS K7105の方法に準拠
して、上記方法により得られたプレートの曇価を測定し
た。 耐衝撃性;上記方法で得られたプレート表面中央部に、
先端が1/2インチRの撃芯をあて、このプレート反対
面に1kgの重りを落下させ、このプレートが割れる高
さを測定した。 流動性;3mm厚みで、15x200mmサイズの射出
成形用金型を用意し、この金型に樹脂組成物を射出成形
し、得られた棒状体の長さを測定した。Transparency: The haze value of the plate obtained by the above method was measured according to the method of JIS K7105. Impact resistance: In the center of the plate surface obtained by the above method,
A tip with a 1/2 inch R tip was applied, a 1 kg weight was dropped on the opposite surface of the plate, and the height at which the plate was cracked was measured. Fluidity: An injection mold having a thickness of 3 mm and a size of 15 × 200 mm was prepared, the resin composition was injection-molded in the mold, and the length of the obtained rod was measured.
【0019】[0019]
【表1】 [Table 1]
【0020】表1から明らかなように、この発明の実施
例1〜5の樹脂組成物は、曇価が低く透明性に優れ、耐
衝撃性もあり、流動性も良い。As is clear from Table 1, the resin compositions of Examples 1 to 5 of the present invention have low haze value, excellent transparency, good impact resistance, and good fluidity.
【0021】これに対して、この発明の範囲を逸脱する
比較例1〜6の樹脂組成物は、透明性、耐衝撃性、流動
性のうち少なくとも1つの性能に劣っていた。即ち、ポ
リカーボネート樹脂が、本発明の好適範囲より多い比較
例1では流動性が劣っていた。ポリカーボネート樹脂が
好適範囲より少ない比較例2、3では耐衝撃性が劣って
いた。PCTGが好適範囲より少ないか、あるいは全く
含まれていない比較例4、5では透明性が劣っていた。
ポリエステル樹脂のグリコール系重縮合成分中、1,4
−シクロヘキサンジメタノールの含有量がPCTGのそ
れより少ない比較例6でも透明性が劣っていた。On the other hand, the resin compositions of Comparative Examples 1 to 6, which deviate from the scope of the present invention, were inferior in at least one of transparency, impact resistance and fluidity. That is, in Comparative Example 1 in which the polycarbonate resin was more than the preferred range of the present invention, the fluidity was poor. In Comparative Examples 2 and 3 where the polycarbonate resin was less than the preferred range, the impact resistance was poor. In Comparative Examples 4 and 5, in which PCTG was less than the preferred range or was not contained at all, the transparency was poor.
In the glycol-based polycondensation component of the polyester resin, 1,4
Comparative Example 6, in which the content of cyclohexanedimethanol was smaller than that of PCTG, was also inferior in transparency.
【0022】[0022]
【発明の効果】以上のように、この発明に係る樹脂組成
物は、ポリカーボネート樹脂に特定のポリエステル樹脂
を配合することにより、ポリカーボネート樹脂の透明
性、耐衝撃性を維持したうえで、その流動性を改善でき
る。As described above, the resin composition according to the present invention maintains the transparency and impact resistance of the polycarbonate resin by blending the specific polyester resin with the polycarbonate resin, and maintains the fluidity of the polycarbonate resin. Can be improved.
Claims (1)
ポリエステル樹脂5〜95重量部とよりなる混合樹脂に
おいて、ポリエステル樹脂の少なくとも1種類が、テレ
フタル酸およびテレフタル酸誘導体からなる郡より選ば
れる1種または2種以上のテレフタル酸系成分からなる
ジカルボン酸系重縮合成分と、1,4−シクロヘキサン
ジメタノールを40モル%以上含有するグリコール系重
縮合成分とを重縮合させて得られる下記一般式(I); 【化1】 で表される反復単位を構造中に有するポリエステル樹脂
(PCTGと呼ぶ)であり、該PCTGの重量比が全体
のポリエステル樹脂成分の10%以上であることを特徴
とする樹脂組成物。(1) 95 to 5 parts by weight of a polycarbonate resin;
In a mixed resin comprising 5 to 95 parts by weight of a polyester resin, at least one of the polyester resins is a dicarboxylic acid based on one or more terephthalic acid components selected from the group consisting of terephthalic acid and terephthalic acid derivatives. The following general formula (I) obtained by polycondensing a polycondensation component with a glycol-based polycondensation component containing 1,4-cyclohexanedimethanol in an amount of 40 mol% or more; A resin composition comprising a polyester resin (referred to as PCTG) having a repeating unit represented by the following formula in its structure, wherein the weight ratio of the PCTG is 10% or more of the entire polyester resin component.
Priority Applications (1)
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JP2000195439A JP2002012748A (en) | 2000-06-29 | 2000-06-29 | Resin composition |
Applications Claiming Priority (1)
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JP2000195439A JP2002012748A (en) | 2000-06-29 | 2000-06-29 | Resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2002012748A true JP2002012748A (en) | 2002-01-15 |
Family
ID=18694101
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Cited By (9)
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JP2003138126A (en) * | 2001-11-05 | 2003-05-14 | Denki Kagaku Kogyo Kk | Thermoplastic resin sheet and its formed product |
JP2004359220A (en) * | 2003-05-12 | 2004-12-24 | Teijin Chem Ltd | Sheet-like window member and window structure |
JP2005206836A (en) * | 2003-12-25 | 2005-08-04 | Mitsubishi Plastics Ind Ltd | Resin blend composition, sheet and molded article comprising the same |
JP2005239834A (en) * | 2004-02-25 | 2005-09-08 | Tsutsunaka Plast Ind Co Ltd | Polycarbonate-based resin sheet |
JP2006249176A (en) * | 2005-03-09 | 2006-09-21 | Tsutsunaka Plast Ind Co Ltd | Resin composition |
US7204479B2 (en) * | 2003-06-10 | 2007-04-17 | Cooper-Standard Automotive Inc. | Vibration isolator assembly having altered stress characteristics, and method of altering stress characteristics of same |
JP2007231200A (en) * | 2006-03-02 | 2007-09-13 | Mitsubishi Plastics Ind Ltd | Thermoplastic resin sheet |
JP2009270121A (en) * | 2003-05-12 | 2009-11-19 | Teijin Chem Ltd | Sheet-form window member and window structure |
JP2010532407A (en) * | 2007-07-04 | 2010-10-07 | エスケー ケミカルズ カンパニー リミテッド | Polyester / polycarbonate blend with transparency and heat resistance |
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