JPH08169961A - Heat-resistant polyester molding and its production - Google Patents

Heat-resistant polyester molding and its production

Info

Publication number
JPH08169961A
JPH08169961A JP4616695A JP4616695A JPH08169961A JP H08169961 A JPH08169961 A JP H08169961A JP 4616695 A JP4616695 A JP 4616695A JP 4616695 A JP4616695 A JP 4616695A JP H08169961 A JPH08169961 A JP H08169961A
Authority
JP
Japan
Prior art keywords
mol
polyester
dicarboxylic acid
molded article
alkyl group
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
JP4616695A
Other languages
Japanese (ja)
Inventor
Hitoshi Kawamoto
均 川本
Yumi Itou
由実 伊藤
Yoshihiro Hayashi
義博 林
Hiroshi Naito
寛 内藤
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.)
Kanebo Ltd
Original Assignee
Kanebo 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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP4616695A priority Critical patent/JPH08169961A/en
Publication of JPH08169961A publication Critical patent/JPH08169961A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: To obtain a molding which scarecely undergoes a longterm change in properties and is excellent in mechanical strengths, shape retentivity and heat resistance. CONSTITUTION: A polyester molding made of a composition containing a major amount of an aromatic dicarboxylic acid and/or its esterifiable derivative, 1-20mol%, based on the entire dicarboylic acid component, aliphatic dicarboxylic acid and/or its esterifiable derivative, 1-15mol%, based on the entire diol component, dihydroy compound represented by the formula (R1 is a 2-4C alkyl group and R2 , R3 , R4 and R5 are each hydrogen or a 1-4C alkyl group) and at least 85mol%, based on the total diol component, aliphatic diol containing ethylene glycol and/or its esterifiable derivative.

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、優れた耐熱性を有する
ポリエステル成形体およびその製造方法に関する。更に
詳しくは、耐経時変化に優れ、透明、強靭であり、且つ
容易に成形する事が可能な成形体およびその製造方法に
関する。
FIELD OF THE INVENTION The present invention relates to a polyester molded article having excellent heat resistance and a method for producing the same. More specifically, the present invention relates to a molded product which is excellent in aging resistance, is transparent, tough, and can be molded easily, and a method for producing the molded product.

【0002】[0002]

【従来の技術】ポリエステル成形体、特にエチレンテレ
フタレート系成形体は、食品容器に代表される製品等に
その優れた透明性、軽量、衛生性をいかんなく発揮し、
幅広い分野で利用されている。しかし、これらの用途に
おいて上記のごとき成形体は、経時変化に対する弱さか
ら成形後に寸法変化を生じる他に、脆くなって耐衝撃性
等が低下するというポリエステル成形体の欠点を大きく
露呈し、今日までこの改善のために多くの努力がはらわ
れてきた。
2. Description of the Related Art Polyester moldings, particularly ethylene terephthalate moldings, exhibit excellent transparency, light weight and hygiene in products represented by food containers.
It is used in a wide range of fields. However, in these applications, the molded article as described above largely exposes the drawbacks of the polyester molded article that the dimension change occurs after molding due to its weakness with time, and the brittleness reduces the impact resistance and the like. Many efforts have been made to improve this.

【0003】耐経時変化力の向上には、成形体の肉厚
化、多層化による成形体強度の向上や、ヒートセット強
化による結晶化度の向上、容器形状を工夫して残留応力
や歪緩和を計る方法、更にはエチレンテレフタレートの
構成成分に加えて、ブチレンテレフタレートの様な成形
時の応力が比較的低い成分をブレンドする事で成形時の
残留応力・歪を緩和するという方法が提案されてきた。
この様な方法としては、特開平2−30512号公報、
特開平4−63836号公報、特開平4−367433
号公報等が挙げられるが、成形体の肉厚化、多層化によ
る成形体強度の向上は樹脂使用量の増大につながり、ヒ
ートセット強化や容器形状の変更は成形工程の複雑化を
招いたり、また、他成分のブレンドでは透明性の悪化や
リサイクルが困難になる等の欠点があった。
In order to improve the resistance to change with time, the thickness of the molded body is increased, the strength of the molded body is improved by increasing the number of layers, the crystallinity is improved by strengthening heat setting, and the residual stress and strain are relaxed by devising the shape of the container. In addition to ethylene terephthalate constituents, a method of blending a component having relatively low stress during molding such as butylene terephthalate to alleviate residual stress and strain during molding has been proposed. It was
As such a method, JP-A-2-30512,
JP-A-4-63836, JP-A-4-368433
As mentioned in the publication, thickening of the molded body, improvement of the strength of the molded body due to multi-layering leads to an increase in the amount of resin used, and strengthening the heat set or changing the shape of the container leads to a complicated molding process, Further, blending other components has drawbacks such as deterioration of transparency and difficulty in recycling.

【0004】[0004]

【発明が解決しようとする課題】本発明者等は、耐経時
変化向上のためには、成形体を成形する時のポリマー構
造体中の残留応力を低減する事が重要と考え、この点か
ら課題解決のため鋭意検討を重ねた結果、ある特定のポ
リエステル樹脂組成物が、上記欠点を解決し得ることを
見い出し、本発明に到達したものであって、その目的と
するところは成形時の残留応力が低く、寸法安定性を付
与するに必要なガラス転移温度を有する、透明、且つ容
易に成形する事が可能な成形体を得るにある。
The present inventors believe that it is important to reduce the residual stress in the polymer structure during molding of the molded article in order to improve the change with time. As a result of extensive studies for solving the problem, a specific polyester resin composition was found to be able to solve the above-mentioned drawbacks, and the present invention has been achieved. The object is to obtain a transparent and easily molded product having a low stress and a glass transition temperature necessary for imparting dimensional stability.

【0005】[0005]

【課題を解決するための手段】上述の目的は、下記
(A)を主成分とし、さらに下記(B)・(C)・
(D)を含む組成物より構成される事を特徴とするポリ
エステル成形体および(A)・(B)・(C)・(D)
を含む組成物を用いる事を特徴とするポリエステル成形
体の製造方法によって達成される。 (A)芳香族ジカルボン酸および/またはそのエステル
形成性誘導体 (B)脂肪族ジカルボン酸および/またはそのエステル
形成性誘導体を全ジカルボン酸成分100モル%中1〜
20モル% (C)一般式
[Means for Solving the Problems] The above-mentioned object is based on the following (A) as a main component, and the following (B), (C), and
A polyester molded article characterized by comprising a composition containing (D), and (A), (B), (C), (D)
It is achieved by a method for producing a polyester molded article, which comprises using a composition containing (A) aromatic dicarboxylic acid and / or its ester-forming derivative (B) aliphatic dicarboxylic acid and / or its ester-forming derivative in 1 to 100 mol% of all dicarboxylic acid components
20 mol% (C) General formula

【化2】 (R1 は炭素数2〜4のアルキル基、R2 , R3 , R4
およびR5 は独立に水素または炭素数1〜4のアルキル
基)で示されるジヒドロキシ化合物を全ジオール成分1
00モル%中1〜15モル% (D)エチレングリコールを含む脂肪族ジオールおよび
/またはそのエステル形成性誘導体を全ジオール成分1
00モル%中85モル%以上
Embedded image (R 1 is an alkyl group having 2 to 4 carbon atoms, R 2 , R 3 , R 4
And R 5 are independently hydrogen or an alkyl group having 1 to 4 carbon atoms) and a dihydroxy compound represented by total diol component 1
1 to 15 mol% in 00 mol% (D) Aliphatic diol containing ethylene glycol and / or its ester-forming derivative is a total diol component 1
85 mol% or more in 00 mol%

【0006】以下、本発明を詳しく説明する。本発明に
おいて用いられる(A)芳香族ジカルボン酸(および/
またはそのエステル形成性誘導体)を構成する成分と
は、テレフタレートのホモポリマーを含む実質的に線上
のコポリエステルを意味する。構成成分の例としては、
テレフタル酸、イソフタル酸、2,6−ナフタレンジカ
ルボン酸、2, 5−ジメチルテレフタル酸、1, 4−ナ
フタレンジカルボン酸、ビフェニルジカルボン酸等の芳
香族ジカルボン酸(および/またはそのエステル形成性
誘導体)等が挙げられる。
Hereinafter, the present invention will be described in detail. (A) Aromatic dicarboxylic acid (and / or) used in the present invention
Alternatively, the component constituting the ester-forming derivative thereof means a substantially linear copolyester containing a homopolymer of terephthalate. Examples of components include:
Aromatic dicarboxylic acids (and / or their ester-forming derivatives) such as terephthalic acid, isophthalic acid, 2,6-naphthalenedicarboxylic acid, 2,5-dimethylterephthalic acid, 1,4-naphthalenedicarboxylic acid, biphenyldicarboxylic acid, etc. Is mentioned.

【0007】また、(B)脂肪族ジカルボン酸(および
/またはそのエステル形成性誘導体)構成成分の例とし
ては、アジピン酸、ピメリン酸、アゼライン酸、セバシ
ン酸等の脂肪族ジカルボン酸(および/またはそのエス
テル形成性誘導体)等が挙げられ、化合物量としては全
ジカルボン酸成分100モル%中1〜20モル%、好ま
しくは3〜15モル%である。化合物量が1モル%未満
では期待した耐経時変化に対する強さが得られず、ま
た、20モル%を超えるとポリエステルそのものの結晶
化速度が小さくなり、成形体としての用途に用いる事が
出来なくなる。
Examples of the component (B) aliphatic dicarboxylic acid (and / or ester-forming derivative thereof) include adipic acid, pimelic acid, azelaic acid, sebacic acid and the like (and / or The ester-forming derivative) and the like are mentioned, and the amount of the compound is 1 to 20 mol%, preferably 3 to 15 mol% in 100 mol% of all dicarboxylic acid components. If the amount of the compound is less than 1 mol%, the expected strength against aging resistance cannot be obtained, and if it exceeds 20 mol%, the crystallization rate of the polyester itself becomes small and it cannot be used as a molded product. .

【0008】(C)一般式(C) General formula

【化3】 (R1 は炭素数2〜4のアルキル基、R2 , R3 , R4
およびR5 は独立に水素または炭素数1〜4のアルキル
基)で示されるジヒドロキシ化合物構成成分の例として
は、9, 9−ビス−(4−ヒドロキシエトキシフェニ
ル)−フルオレン、9, 9−ビス−(4−ヒドロキシプ
ロポキシフェニル)−フルオレン、9, 9−ビス−(4
−ヒドロキシブトキシフェニル)−フルオレン等がある
が、成形性や重合の行い易さの点から特に9, 9−ビス
−(4−ヒドロキシエトキシフェニル)−フルオレンが
好ましい。前記ポリエステルの一般式(1)で表される
ジヒドロキシ化合物の量としては、1〜15モル%、好
ましくは5〜10モル%である。化合物量が1モル%未
満では期待した耐熱性が得られず、また、15モル%を
超えるとポリエステルそのものの結晶化速度が小さくな
り、延伸成形体としての用途に用いる事が出来なくな
る。
Embedded image (R 1 is an alkyl group having 2 to 4 carbon atoms, R 2 , R 3 , R 4
And R 5 are independently hydrogen or an alkyl group having 1 to 4 carbon atoms). Examples of dihydroxy compound constituents include 9,9-bis- (4-hydroxyethoxyphenyl) -fluorene and 9,9-bis -(4-hydroxypropoxyphenyl) -fluorene, 9,9-bis- (4
-Hydroxybutoxyphenyl) -fluorene and the like are preferable, but 9,9-bis- (4-hydroxyethoxyphenyl) -fluorene is particularly preferable from the viewpoint of moldability and ease of polymerization. The amount of the dihydroxy compound represented by the general formula (1) of the polyester is 1 to 15 mol%, preferably 5 to 10 mol%. If the amount of the compound is less than 1 mol%, the expected heat resistance cannot be obtained, and if it exceeds 15 mol%, the crystallization rate of the polyester itself becomes small, and it cannot be used for a stretch molded product.

【0009】9, 9−ビス−(4−ヒドロキシエトキシ
フェニル)−フルオレンは、例えば、9, 9−ビス−
(4−ヒドロキシフェニル)−フルオレンにエチレンオ
キサイド(以下、EOと略記する。)を付加して得られ
る。この際、フェノールの両水酸基にエチレンオキサイ
ドが1分子ずつ付加した2EO付加体、(9, 9−ビス
−(4−ヒドロキシエトキシフェニル)−フルオレン)
の他に、さらに数分子過剰に付加した、3EO,4EO
付加体等の不純物が含まれる事がある。3EO,4EO
などの不純物が多くなると、ポリエステル重合体の耐熱
性を低下させる事になる。このときの2EO付加体の純
度は85%以上有れば良いが、好ましくは95%以上で
ある。
9,9-bis- (4-hydroxyethoxyphenyl) -fluorene is, for example, 9,9-bis-
It is obtained by adding ethylene oxide (hereinafter abbreviated as EO) to (4-hydroxyphenyl) -fluorene. At this time, a 2EO adduct obtained by adding one molecule of ethylene oxide to both hydroxyl groups of phenol, (9,9-bis- (4-hydroxyethoxyphenyl) -fluorene)
In addition to 3EO and 4EO
Impurities such as adducts may be contained. 3EO, 4EO
When the amount of such impurities as described above increases, the heat resistance of the polyester polymer decreases. At this time, the purity of the 2EO adduct may be 85% or more, preferably 95% or more.

【0010】9, 9−ビス−(4−ヒドロキシプロポキ
シフェニル)−フルオレン、9, 9−ビス−(4−ヒド
ロキシブトキシフェニル)−フルオレンは、例えば、
9, 9−ビス−(4−ヒドロキシフェニル)−フルオレ
ンに各々、3−クロロ−プロパン−1−オール、4−ク
ロロ−プロパン−1−オールをアルカリ性条件下で反応
させれば得られる。この際の純度も、85%以上で有れ
ば良く、好ましくは95%以上である。
Examples of 9,9-bis- (4-hydroxypropoxyphenyl) -fluorene and 9,9-bis- (4-hydroxybutoxyphenyl) -fluorene include:
It can be obtained by reacting 9,9-bis- (4-hydroxyphenyl) -fluorene with 3-chloro-propan-1-ol and 4-chloro-propan-1-ol, respectively, under alkaline conditions. The purity at this time may be 85% or more, and preferably 95% or more.

【0011】(D)エチレングリコールを含む脂肪族ジ
オールおよび/またはそのエステル形成性誘導体の構成
成分としては、エチレングリコールの他に、ジエチレン
グリコール、ポリエチレングリコール、ポリメチレング
リコール、テトラメチレングリコール、1, 4−ブタン
ジオールのグリコール等が挙げられ、その化合物量は結
晶性を維持するという点で85モル%以上である。
(D) As constituent components of the aliphatic diol containing ethylene glycol and / or its ester-forming derivative, in addition to ethylene glycol, diethylene glycol, polyethylene glycol, polymethylene glycol, tetramethylene glycol, 1,4- Examples include butanediol glycol and the like, and the amount of the compound is 85 mol% or more from the viewpoint of maintaining crystallinity.

【0012】以上に述べた(A)〜(D)の成分は、各
々その1種又は2種以上を含んでいてもよい。
The components (A) to (D) described above may each contain one type or two or more types.

【0013】本発明の上記(A)〜(D)より構成され
るポリエステル組成物は、例えば、エステル交換法、直
接交換法等の溶融重合法、溶液重合法、界面重合法、樹
脂ブレンド等の公知方法からの適宜の方法を選択して製
造出来る。また重合の際の触媒については、二酸化ゲル
マニウム、チタンテトラブトキシド、三酸化アンチモ
ン、酢酸アンチモン等が挙げられるが、色調に優れ食品
衛生上より安全であるという点で二酸化ゲルマニウムが
より好ましい。これらの反応条件についても従来通りで
良く、公知の方法を用いる事ができる。
The polyester composition comprising the above (A) to (D) of the present invention may be, for example, a melt polymerization method such as a transesterification method or a direct exchange method, a solution polymerization method, an interfacial polymerization method or a resin blending method. It can be produced by selecting an appropriate method from known methods. Examples of the catalyst for the polymerization include germanium dioxide, titanium tetrabutoxide, antimony trioxide, antimony acetate and the like, but germanium dioxide is more preferable because it has an excellent color tone and is safer for food hygiene. These reaction conditions may be the same as conventional ones, and known methods can be used.

【0014】また、成形体の製造方法については、上記
(A)〜(D)を含む組成物を使用する以外は従来公知
の方法として用いる事が出来る。例えば、真空、圧空、
真空圧空成形、プレス成形、ブロー成形等である。
Further, as a method for producing a molded article, a conventionally known method can be used except that the composition containing the above (A) to (D) is used. For example, vacuum, compressed air,
Vacuum pressure molding, press molding, blow molding and the like.

【0015】[0015]

【発明の効果】本発明のポリエステル樹脂組成物は、食
品包装材料等の用途において、経時変化による物性変化
の影響を受け難く、機械強度、形状保持力等に優れた耐
熱性良好な製品であり、透明性を損なう事なく、成形性
良好な極めて有用な組成物である。作製された成形体の
用途としては、二軸延伸ボトル容器等の各種・各形状の
容器を含めた広い範囲で使用可能である。
INDUSTRIAL APPLICABILITY The polyester resin composition of the present invention is a product having good heat resistance, which is not easily affected by changes in physical properties due to aging and is excellent in mechanical strength, shape retention, etc., in applications such as food packaging materials. It is a very useful composition with good moldability without impairing transparency. The produced molded product can be used in a wide range including various-shaped containers such as biaxially stretched bottle containers.

【0016】[0016]

【実施例】以下実施例を挙げて本発明を具体的に説明す
る。実施例における組成物のガラス転移温度、収縮開始
温度、衝撃値は以下に示す方法で測定した。尚、本発明
はこれらの実施例に限定されるものではない。
EXAMPLES The present invention will be specifically described with reference to the following examples. The glass transition temperature, shrinkage initiation temperature, and impact value of the compositions in the examples were measured by the methods described below. The present invention is not limited to these examples.

【0017】(1)ガラス転移温度 PERKIN−ELMER社製示差走査熱量測定装置
(DSC)にて、試料約10mgを用いて、昇温速度1
0℃/min におけるガラス転移温度(Tg)を採用した。
尚、本発明のガラス転移温度とは、示差走差熱量測定
(DSC)の昇温過程においてJIS−K7121にて
規定するガラス転移開始温度(Tig )を使用する。
(1) Glass transition temperature Using a differential scanning calorimeter (DSC) manufactured by PERKIN-ELMER, about 10 mg of a sample was used, and the heating rate was 1
The glass transition temperature (Tg) at 0 ° C / min was adopted.
The glass transition temperature of the present invention means the glass transition start temperature (Tig) specified in JIS-K7121 in the temperature rising process of differential scanning calorimetry (DSC).

【0018】(2)収縮開始温度 理学電機社製熱機械分析装置(TMA)を用いて、延伸
倍率が×3.2倍であるサンプルの、荷重10g、昇温
速度10℃/min にて引っ張り荷重法における収縮開始
温度を採用した。
(2) Shrinkage onset temperature Using a thermomechanical analyzer (TMA) manufactured by Rigaku Denki Co., Ltd., a sample having a draw ratio of × 3.2 was pulled at a load of 10 g and a heating rate of 10 ° C./min. The shrinkage initiation temperature in the loading method was adopted.

【0019】(3)衝撃値 東洋精機社製グラフィックインパクトテスターを用い
て、試験高さは延伸倍率×1.5倍フィルム:30cm、
延伸倍率×3.2倍フィルム:20cmにて荷重6.5k
g、23℃におけるフィルム破壊時の亀裂発生エネルギ
ー値を採用した。
(3) Impact value Using a graphic impact tester manufactured by Toyo Seiki Co., Ltd., the test height is a draw ratio x1.5 times film: 30 cm,
Stretching ratio x 3.2 times Film: Load at 20 cm, 6.5k
The energy value of crack generation at film breakage at 23 ° C. was adopted.

【0020】評価用サンプル作製方法 樹脂を270〜290℃で溶融、N2 雰囲気下、真空プ
レス成形で、直径130mm,厚さ約500μmの円盤
状の試験片を作製した。延伸倍率は2条件で評価するも
のとし、延伸(×1.5倍)、延伸(×3.2倍)
とした。95℃×2分で予熱、縦横延伸速度5m/mi
nの条件にて延伸し、厚み5〜100μmのフィルムを
得た。その後120℃×30秒間ヒートセット処理を行
った。
Method of preparing sample for evaluation A resin-like test piece having a diameter of 130 mm and a thickness of about 500 .mu.m was prepared by melting the resin at 270 to 290.degree. Stretching ratio shall be evaluated under two conditions: stretching (× 1.5 times), stretching (× 3.2 times)
And Preheat at 95 ℃ x 2 minutes, stretching speed 5m / mi
The film was stretched under the condition of n to obtain a film having a thickness of 5 to 100 μm. Then, heat setting treatment was performed at 120 ° C. for 30 seconds.

【0021】経時変化を進めるためのエージング処理条
件としては、40℃×65%RH×1weekにて空気
中に放置した。
As the aging treatment condition for promoting the change with time, the film was left in the air at 40 ° C. × 65% RH × 1 week.

【0022】(実施例1)テレフタル酸ジメチル 95
重量部、アジピン酸ジメチル 5重量部、9,9−ビス
−(4−ヒドロキシエトキシフェニル)−フルオレン
10重量部、エチレングリコール 90重量部を原料と
し、触媒として酢酸カルシウム 0.025重量部を用
い、これらを反応槽に投入し、撹拌しながら常法にした
がって180℃から230℃に徐々に加熱してエステル
交換反応を行った。所定量のメタノールを系外へ抜き出
した後、重合触媒である二酸化ゲルマニウム 0.01
5重量部と、着色を防止するため、リン酸トリメチル
0.008重量部とを投入して、昇温と減圧を徐々に行
い、発生するエチレングリコールを抜きながら、加熱槽
温度を280℃、真空度を1Torr以下に到達させ
た。この条件を維持し、粘度の上昇を待ち、撹拌機にか
かるトルクが所定の値に達した時点で反応を終了し、反
応物を水中に押し出してペレットを得た。こうして得ら
れたペレットをカッターにてチップ化し、220℃×1
2Hr×5Torr以下の減圧下にて固相重合を実施し
た。
(Example 1) Dimethyl terephthalate 95
Parts by weight, dimethyl adipate 5 parts by weight, 9,9-bis- (4-hydroxyethoxyphenyl) -fluorene
10 parts by weight and 90 parts by weight of ethylene glycol were used as raw materials, and 0.025 parts by weight of calcium acetate was used as a catalyst. These were put into a reaction tank and gradually heated from 180 ° C. to 230 ° C. according to a conventional method with stirring. Transesterification was carried out. After extracting a predetermined amount of methanol out of the system, the polymerization catalyst germanium dioxide 0.01
5 parts by weight and trimethyl phosphate to prevent coloring
0.008 parts by weight was added, the temperature was raised and the pressure was gradually reduced, and the heating tank temperature was 280 ° C. and the degree of vacuum was 1 Torr or less while removing the generated ethylene glycol. While maintaining this condition, waiting for the increase in viscosity, the reaction was terminated when the torque applied to the stirrer reached a predetermined value, and the reaction product was extruded into water to obtain pellets. The pellets thus obtained are chipped with a cutter, and 220 ° C x 1
Solid phase polymerization was carried out under reduced pressure of 2 Hr × 5 Torr or less.

【0023】この組成物の固相重合後のガラス転移温度
は82℃であった。上記した評価用サンプル作製方法に
従って、ヒートセット処理した後の延伸フィルムの収縮
開始温度を測定したところ温度は98℃、衝撃値(亀裂
発生エネルギー)は延伸倍率×1.5倍:1.8J、延
伸倍率×3.2倍:2.7Jであった。更にこの後エー
ジング処理により経時変化の進んだサンプルフィルムの
測定値は、順にそれぞれ98℃、1.6J、2.9Jで
あった。以上の測定結果を表1に示す。
The glass transition temperature of this composition after solid state polymerization was 82 ° C. When the shrinkage initiation temperature of the stretched film after the heat setting treatment was measured according to the above-described evaluation sample preparation method, the temperature was 98 ° C., and the impact value (crack generation energy) was a draw ratio × 1.5 times: 1.8 J, The draw ratio was 3.2 times: 2.7J. After that, the measured values of the sample film which has been aged over time due to the aging treatment were 98 ° C., 1.6 J and 2.9 J, respectively. Table 1 shows the above measurement results.

【0024】(実施例2)原料組成比を表1に示す様に
変更する以外は、実施例1と同様にして経時変化前後の
物性評価を実施した。測定結果を表1に示す。
Example 2 The physical properties before and after the change with time were evaluated in the same manner as in Example 1 except that the raw material composition ratio was changed as shown in Table 1. Table 1 shows the measurement results.

【0025】(比較例1〜5)原料組成比を表1に示す
様に変更する以外は、実施例1と同様にして経時変化前
後の物性評価を実施した。測定結果を表1に示す。
Comparative Examples 1 to 5 Physical properties before and after the change with time were evaluated in the same manner as in Example 1 except that the raw material composition ratio was changed as shown in Table 1. Table 1 shows the measurement results.

【0026】表1から明かな様に、実施例1、2はエー
ジング処理実施後も、延伸の様な低延伸倍率の部分に
ついて脆弱化が検出されず、倍率による強度のばらつき
が抑えられた優れた物性を維持している事がわかる。こ
れに対し比較例1〜5は経時変化により低延伸倍率部分
の脆弱化、非晶化等がみられ、耐衝撃値の低下、成形性
悪化、熱安定性悪化等の影響が発現している。
As is clear from Table 1, in Examples 1 and 2, even after the aging treatment, the brittleness was not detected in the portion having a low stretch ratio such as stretching, and the variation in strength depending on the stretch ratio was excellent. It can be seen that the physical properties are maintained. On the other hand, in Comparative Examples 1 to 5, weakening, amorphization and the like of the low draw ratio portion were observed due to aging, and impacts such as a reduction in impact resistance, deterioration of moldability and deterioration of thermal stability were exhibited. .

【0027】以上の事から、本発明による組成物は、経
時変化に対する安定性、耐熱性、透明性が良く、更に成
形性にも優れたものであることが判る。
From the above, it can be seen that the composition according to the present invention has good stability with respect to aging, heat resistance and transparency, and is also excellent in moldability.

【表1】 [Table 1]

─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成7年4月26日[Submission date] April 26, 1995

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0020[Correction target item name] 0020

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0020】評価用サンプル作製方法 樹脂を270〜290℃で溶融、N2 雰囲気下、真空プ
レス成形で、直径130mm、厚さ約500μmの円盤
状の試験片を作製した。延伸倍率は2条件で評価するも
のとし、延伸(×1.5倍)、延伸(×3.2倍)
とした。95℃×2分で予熱、縦横延伸速度5m/mi
nの条件にて延伸し、厚み50〜100μmのフィルム
を得た。その後120℃×30秒間ヒートセット処理を
行った。
Method for preparing sample for evaluation A resin-like test piece having a diameter of 130 mm and a thickness of about 500 μm was prepared by melting the resin at 270 to 290 ° C. and vacuum press forming in an N 2 atmosphere. Stretching ratio shall be evaluated under two conditions: stretching (× 1.5 times), stretching (× 3.2 times)
And Preheat at 95 ℃ x 2 minutes, stretching speed 5m / mi
The film was stretched under the condition of n to obtain a film having a thickness of 50 to 100 μm. Then, heat setting treatment was performed at 120 ° C. for 30 seconds.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 下記(A)を主成分とし、さらに下記
(B)・(C)・(D)を含む組成物より構成される事
を特徴とするポリエステル成形体。 (A)芳香族ジカルボン酸および/またはそのエステル
形成性誘導体 (B)脂肪族ジカルボン酸および/またはそのエステル
形成性誘導体を全ジカルボン酸成分100モル%中1〜
20モル% (C)一般式 【化1】 (R1 は炭素数2〜4のアルキル基、R2 , R3 , R4
およびR5 は独立に水素または炭素数1〜4のアルキル
基)で示されるジヒドロキシ化合物を全ジオール成分1
00モル%中1〜15モル% (D)エチレングリコールを含む脂肪族ジオールおよび
/またはそのエステル形成性誘導体を全ジオール成分1
00モル%中85モル%以上
1. A polyester molded article comprising a composition containing the following (A) as a main component and further containing the following (B), (C), and (D). (A) aromatic dicarboxylic acid and / or its ester-forming derivative (B) aliphatic dicarboxylic acid and / or its ester-forming derivative in 1 to 100 mol% of all dicarboxylic acid components
20 mol% (C) General formula: (R 1 is an alkyl group having 2 to 4 carbon atoms, R 2 , R 3 , R 4
And R 5 are independently hydrogen or an alkyl group having 1 to 4 carbon atoms) and a dihydroxy compound represented by total diol component 1
1 to 15 mol% in 00 mol% (D) Aliphatic diol containing ethylene glycol and / or its ester-forming derivative is a total diol component 1
85 mol% or more in 00 mol%
【請求項2】 一般式(1)で示されるジヒドロキシ化
合物が9,9−ビス−(4−ヒドロキシエトキシフェニ
ル)−フルオレンである事を特徴とする請求項1に記載
のポリエステル成形体。
2. The polyester molded article according to claim 1, wherein the dihydroxy compound represented by the general formula (1) is 9,9-bis- (4-hydroxyethoxyphenyl) -fluorene.
【請求項3】 ポリエステル樹脂組成物を成形してポリ
エステル成形体を製造するに際し、ポリエステル樹脂組
成物として請求項1に記載の(A)・(B)・(C)・
(D)を含む組成物を用いることを特徴とするポリエス
テル成形体の製造方法。
3. When the polyester resin composition is molded to produce a polyester molded article, the polyester resin composition as described in (A). (B). (C).
A method for producing a polyester molded article, which comprises using a composition containing (D).
【請求項4】 一般式(1)で示されるジヒドロキシ化
合物が9,9−ビス−(4−ヒドロキシエトキシフェニ
ル)−フルオレンである事を特徴とする請求項3に記載
のポリエステル成形体の製造方法。
4. The method for producing a polyester molded article according to claim 3, wherein the dihydroxy compound represented by the general formula (1) is 9,9-bis- (4-hydroxyethoxyphenyl) -fluorene. .
JP4616695A 1994-10-18 1995-02-09 Heat-resistant polyester molding and its production Pending JPH08169961A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4616695A JPH08169961A (en) 1994-10-18 1995-02-09 Heat-resistant polyester molding and its production

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP6-279929 1994-10-18
JP27992994 1994-10-18
JP4616695A JPH08169961A (en) 1994-10-18 1995-02-09 Heat-resistant polyester molding and its production

Publications (1)

Publication Number Publication Date
JPH08169961A true JPH08169961A (en) 1996-07-02

Family

ID=26386285

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4616695A Pending JPH08169961A (en) 1994-10-18 1995-02-09 Heat-resistant polyester molding and its production

Country Status (1)

Country Link
JP (1) JPH08169961A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000355091A (en) * 1999-04-14 2000-12-26 Toyobo Co Ltd Container moldable improved polyester sheet and heat- resistant polyester molded article using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000355091A (en) * 1999-04-14 2000-12-26 Toyobo Co Ltd Container moldable improved polyester sheet and heat- resistant polyester molded article using the same

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