JP2002053741A - Processability improver for pet-g resin, and pet-g resin composition - Google Patents

Processability improver for pet-g resin, and pet-g resin composition

Info

Publication number
JP2002053741A
JP2002053741A JP2000238259A JP2000238259A JP2002053741A JP 2002053741 A JP2002053741 A JP 2002053741A JP 2000238259 A JP2000238259 A JP 2000238259A JP 2000238259 A JP2000238259 A JP 2000238259A JP 2002053741 A JP2002053741 A JP 2002053741A
Authority
JP
Japan
Prior art keywords
pet
acid
resin
ester
improver
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
JP2000238259A
Other languages
Japanese (ja)
Other versions
JP4633892B2 (en
Inventor
Takayuki Sakagami
高行 阪上
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.)
Riken Vitamin Co Ltd
Original Assignee
Riken Vitamin 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 Riken Vitamin Co Ltd filed Critical Riken Vitamin Co Ltd
Priority to JP2000238259A priority Critical patent/JP4633892B2/en
Publication of JP2002053741A publication Critical patent/JP2002053741A/en
Application granted granted Critical
Publication of JP4633892B2 publication Critical patent/JP4633892B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide an improver which gives an excellent calendaring processability without hindering the transparency of PET-G product to be obtained and to provide a PET-G resin composition containing the improver. SOLUTION: The processability improver for PET-G resins, comprising an ester which is constituted with an aliphatic compound having a hydroxyl group in the molecule and a polybasic acid, is characterized in that the improver has as the main component a mixture of one or more kinds of the esters in which at least one free carboxylic group remains on one molecule of the above ester; the PET-G resin composition contains this processability improver.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、例えば、PET−
G樹脂のカレンダー加工における成形加工性改良剤及び
当該改良剤を含有したPET−G樹脂組成物に関する。
TECHNICAL FIELD The present invention relates to, for example, PET-
The present invention relates to a moldability improver in calendering of a G resin and a PET-G resin composition containing the improver.

【0002】[0002]

【従来の技術】ポリエチレンテレフタレート(PET)
等のポリエステル系樹脂は、食品や医薬品の容器・包装
資材、電子機器、事務用品等のケース類や成形された容
器用蓋材、あるいは、IDカード用シート等として用途
が広がっている。
2. Description of the Related Art Polyethylene terephthalate (PET)
Polyester-based resins such as are widely used as containers and packaging materials for foods and pharmaceuticals, electronic equipment, office supplies and other cases, molded container lids, and ID card sheets.

【0003】これらポリエステル系樹脂のフィルムやシ
ートの成形加工は押出し加工によるのが一般的であっ
た。しかしながら、押出し加工による成形では成形速度
が遅く、生産性が良好とは言えない。一方、フィルムや
シートの成形において生産性の高い方法としてはカレン
ダー加工法があり、塩化ビニル樹脂シート等には従来か
ら使用されている。
[0003] In general, these polyester resin films and sheets are formed by extrusion. However, the molding speed in extrusion molding is low, and the productivity is not good. On the other hand, as a method of high productivity in forming a film or a sheet, there is a calendering method, which has been conventionally used for a vinyl chloride resin sheet or the like.

【0004】このカレンダー加工によりフィルムやシー
トを成形する際には、樹脂を十分に溶融させる必要があ
るが、溶融によってポリエステル系樹脂はカレンダーロ
ールに強く粘着して加工が困難になる。溶融を抑え、加
工温度を低くするとロール面への樹脂の粘着は改善され
るが、成形されたフィルムやシートの表面が荒れるとい
う問題が生じ満足のいく製品が得られない。
When a film or sheet is formed by this calendering process, it is necessary to sufficiently melt the resin. However, the melting causes the polyester resin to strongly adhere to the calender rolls, making the processing difficult. When the melting is suppressed and the processing temperature is lowered, the adhesion of the resin to the roll surface is improved, but the surface of the formed film or sheet becomes rough, and a satisfactory product cannot be obtained.

【0005】ポリエステル系樹脂としてはPET樹脂が
一般的で広く普及されているが、PET樹脂は結晶性が
大きいためにカレンダー加工によるフィルムやシートの
製造は困難である。
[0005] PET resins are generally and widely used as polyester-based resins, but it is difficult to produce films and sheets by calendering because PET resins have high crystallinity.

【0006】この結晶性に起因するPET樹脂の欠点を
改良した樹脂として、ポリエチレンテレフタレートのエ
チレングリコール成分の一部をシクロヘキサンジメタノ
ールで置換し変性させ非結晶としたコポリエステルであ
るグリコール変性PET(本明細書において、PET−
Gという。)が開発され販売されているが、ポリエステ
ル樹脂の特性であるカレンダー加工でのロール表面への
粘着という問題は解決されていない。
As a resin in which the disadvantages of the PET resin caused by the crystallinity are improved, glycol-modified PET (this product) is a non-crystalline copolyester which is modified by replacing a part of the ethylene glycol component of polyethylene terephthalate with cyclohexane dimethanol and modifying it. In the description, PET-
G. ) Has been developed and sold, but the problem of sticking to the roll surface during calendering, which is a property of polyester resins, has not been solved.

【0007】このようなポリエステル系樹脂のカレンダ
ー加工での問題を改善する方法としては、ポリエチレン
テレフタレート樹脂のエチレングリコール成分を10〜
40モル%シクロヘキサンジメタノールに置換してなる
共重合ポリエステルに、ブチルステアレート、セチルパ
ルミテート、ステアリン酸モノグリセライド、ステアリ
ン酸ジグリセライド、ステアリン酸トリグリセライド、
モンタン酸のエステル、カルシウムで部分鹸化したモン
タン酸のエステル、ロウエステル、脂肪族ジカルボン酸
エステル等の脂肪酸エステル系の滑剤を使用することが
開示されている(特開平11−343353号公報)。
しかしながら、当該公報に開示された脂肪酸エステル類
では効果が十分でなく、満足なロール剥離性が得られ
ず、剥離性を得るために添加量を多くするとシートが白
濁する問題が生ずる。
[0007] As a method of solving such a problem in calendering of a polyester resin, there is known a method in which the ethylene glycol component of a polyethylene terephthalate resin is reduced to 10 to 10%.
Butyl stearate, cetyl palmitate, stearic acid monoglyceride, stearic acid diglyceride, stearic acid triglyceride,
It is disclosed that a fatty acid ester lubricant such as an ester of montanic acid, an ester of montanic acid partially saponified with calcium, a wax ester, or an aliphatic dicarboxylic acid ester is used (Japanese Patent Application Laid-Open No. 11-343353).
However, the fatty acid esters disclosed in this publication are not sufficiently effective, fail to provide satisfactory roll releasability, and cause a problem that the sheet becomes cloudy if the amount of addition is increased to obtain releasability.

【0008】このようなことから、透明性を阻害しない
ロール剥離性の良好なポリエステル系樹脂用加工性改良
剤が望まれていた。
[0008] For these reasons, there has been a demand for a processability improver for polyester resins having good roll releasability which does not hinder transparency.

【0009】[0009]

【発明が解決しようとする課題】本発明は、得られたP
ET−G製品の透明性を阻害することなく、優れたカレ
ンダー加工性をもたらす改良剤及びその改良剤を含有し
たPET−G樹脂組成物を提供することを課題とする。
SUMMARY OF THE INVENTION The present invention relates to the obtained P
It is an object of the present invention to provide an improver that provides excellent calenderability without impairing the transparency of an ET-G product, and a PET-G resin composition containing the improver.

【0010】[0010]

【課題を解決するための手段】本発明者は、上記課題を
解決するために鋭意研究を重ねた結果、分子内に水酸基
を有する脂肪族化合物と多塩基酸とからなるエステルで
あり、当該エステル1分子当たり少なくとも1個の遊離
カルボキシル基が残存するエステルが、PET−G製品
の透明性を阻害することなく、優れたカレンダー加工性
をもたらすことを見出し本発明を完成したものである。
Means for Solving the Problems The inventors of the present invention have made intensive studies to solve the above-mentioned problems, and as a result, the present invention relates to an ester comprising an aliphatic compound having a hydroxyl group in a molecule and a polybasic acid, The inventors have found that an ester in which at least one free carboxyl group remains per molecule provides excellent calenderability without impairing the transparency of a PET-G product, and completed the present invention.

【0011】即ち、本発明は以下に記載する構成を有す
るものである。 1.分子内に水酸基を有する脂肪族化合物と多塩基酸と
から構成されるエステルであり、当該エステル1分子当
たり少なくとも1個の遊離カルボキシル基が残存するエ
ステル1種又は2種以上の混合物を主成分とすることを
特徴とするPET−G樹脂用加工性改良剤。
That is, the present invention has the following configuration. 1. An ester composed of an aliphatic compound having a hydroxyl group in the molecule and a polybasic acid, and containing, as a main component, one or a mixture of two or more esters in which at least one free carboxyl group remains per one molecule of the ester. A processability improver for PET-G resin.

【0012】2.分子内に水酸基を有する脂肪族化合物
が、高級脂肪族1価アルコール、又は炭素数2〜6の多
価アルコール及び/又はそれらの重縮合物と高級脂肪酸
との部分エステルであることを特徴とする上記1に記載
のPET−G樹脂用加工性改良剤。
2. The aliphatic compound having a hydroxyl group in the molecule is a higher aliphatic monohydric alcohol or a polyhydric alcohol having 2 to 6 carbon atoms and / or a partial ester of a polycondensate thereof and a higher fatty acid. 2. The processability improver for PET-G resin according to 1 above.

【0013】3.多塩基酸が脂肪族ジカルボン酸又はト
リカルボン酸であることを特徴とする上記1又は2に記
載のPET−G樹脂用加工性改良剤。
3. 3. The processability improver for PET-G resin according to the above 1 or 2, wherein the polybasic acid is an aliphatic dicarboxylic acid or a tricarboxylic acid.

【0014】4.上記1、2又は3に記載の加工性改良
剤を含有することを特徴とするPET−G樹脂組成物。
4. A PET-G resin composition comprising the processability improver described in the above item 1, 2 or 3.

【0015】[0015]

【発明の実施の形態】以下、本発明の詳細について説明
する。本発明が対象とする樹脂は、ポリエチレンテレフ
タレートのエチレングリコール成分の一部をシクロヘキ
サンジメタノールで置換し、変成させた非晶質のコポリ
エステル(PET−G)である。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The details of the present invention will be described below. The resin targeted by the present invention is an amorphous copolyester (PET-G) which is obtained by modifying a part of the ethylene glycol component of polyethylene terephthalate with cyclohexanedimethanol and modifying it.

【0016】本発明の分子内に水酸基を有する脂肪族化
合物と多塩基酸とから構成されるエステルを構成する
「分子内に水酸基を有する脂肪族化合物」としては、例
えば、ラウリルアルコール、ミリスチルアルコール、セ
チルアルコール、ステアリルアルコール、アラキルアル
コール、ベヘニルアルコール等の脂肪族1価アルコー
ル、エチレングリコール、1,2−プロパンジオール、
1,3−プロパンジオール、1,4−ブタンジオール、
2,3−ブタンジオール、1,5−ペンタンジオール、
1,6−ヘキサンジオール、グリセリン、トリメチロー
ルプロパン、エリスリトール、ペンタエリスリトール、
ジペンタエリスリトール、キシリトール、マンニトー
ル、ソルビトール、ソルビタン等の2価〜多価アルコー
ル及び/又はそれらの重縮合物、あるいはこれらの多価
アルコールとカプリル酸、カプリン酸、ラウリン酸、ミ
リスチン酸、パルミチン酸、ステアリン酸、ベヘン酸、
オレイン酸、リノール酸、リノレン酸、エルカ酸等の脂
肪族カルボン酸との部分エステル等が挙げられる。
The "aliphatic compound having a hydroxyl group in the molecule" constituting the ester of the present invention composed of an aliphatic compound having a hydroxyl group in the molecule and a polybasic acid includes, for example, lauryl alcohol, myristyl alcohol, Cetyl alcohol, stearyl alcohol, aralkyl alcohol, aliphatic monohydric alcohols such as behenyl alcohol, ethylene glycol, 1,2-propanediol,
1,3-propanediol, 1,4-butanediol,
2,3-butanediol, 1,5-pentanediol,
1,6-hexanediol, glycerin, trimethylolpropane, erythritol, pentaerythritol,
Dipentaerythritol, xylitol, mannitol, sorbitol, dihydric to polyhydric alcohols such as sorbitan and / or polycondensates thereof, or these polyhydric alcohols and caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, Stearic acid, behenic acid,
Examples thereof include partial esters with aliphatic carboxylic acids such as oleic acid, linoleic acid, linolenic acid, and erucic acid.

【0017】本発明の分子内に水酸基を有する脂肪族化
合物と多塩基酸とから構成されるエステルを構成する
「多塩基酸」としては、例えば、シュウ酸、マロン酸、
コハク酸、グルタル酸、アジピン酸、ピメリン酸、スベ
リン酸、アゼライン酸、セバシン酸、マレイン酸、フマ
ル酸、シトラコン酸、イタコン酸、リンゴ酸、酒石酸な
どの脂肪族ジカルボン酸、あるいは、トリカルバリン
酸、クエン酸などの脂肪族トリカルボン酸等が挙げられ
る。
The "polybasic acid" constituting the ester of the present invention composed of an aliphatic compound having a hydroxyl group in the molecule and a polybasic acid includes, for example, oxalic acid, malonic acid,
Aliphatic dicarboxylic acids such as succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, maleic acid, fumaric acid, citraconic acid, itaconic acid, malic acid, tartaric acid, or tricarbaric acid; Examples thereof include aliphatic tricarboxylic acids such as citric acid.

【0018】本発明の分子内に水酸基を有する脂肪族化
合物と多塩基酸とから構成されるエステルは、上記の多
塩基酸と、アルコールの如き分子内に水酸基を有する脂
肪族化合物とのそれぞれ1種又は2種以上の混合物を使
用し、公知の方法によりエステル化反応を行い調製する
ことができる。又、それらの反応物を単独又は混合物と
して使用することが可能である。
The ester of the present invention comprising an aliphatic compound having a hydroxyl group in the molecule and a polybasic acid is one of the above-mentioned polybasic acid and an aliphatic compound having a hydroxyl group in the molecule such as an alcohol. It can be prepared by performing an esterification reaction by a known method using a species or a mixture of two or more species. Further, those reactants can be used alone or as a mixture.

【0019】本発明に係るPET−G樹脂用加工性改良
剤は、本発明のエステル1種又は2種以上の混合物から
成るが、これを主成分とする限り、他の成分を含有して
も構わない。
The processability improver for PET-G resin according to the present invention comprises one or a mixture of two or more of the esters of the present invention. I do not care.

【0020】又、本発明の分子内に水酸基を有する脂肪
族化合物と多塩基酸とから構成されるエステルにおいて
は、その反応物において多塩基酸に由来するカルボキシ
ル基が少なくとも一個残存することが必要であり、多塩
基酸分子のカルボキシル基全てがエステルとして反応に
利用されたエステルは本発明の目的であるポリエステル
系樹脂への改良効果は発現されない。
In the ester of the present invention comprising an aliphatic compound having a hydroxyl group in a molecule and a polybasic acid, it is necessary that at least one carboxyl group derived from the polybasic acid remains in the reaction product. An ester in which all of the carboxyl groups of the polybasic acid molecule are used in the reaction as an ester does not exhibit the effect of improving the polyester resin which is the object of the present invention.

【0021】本発明の分子内に水酸基を有する脂肪族化
合物と多塩基酸とから構成されるエステルをポリエステ
ル系樹脂に配合することにより、PET−G樹脂組成物
のカレンダー成形加工時においてカレンダー表面への粘
着性が改善され、透明性の優れた製品が得られる。
By blending the polyester resin of the present invention with an ester composed of an aliphatic compound having a hydroxyl group in a molecule and a polybasic acid, the surface of the PET-G resin composition is calendered during calendering. Is improved and a product with excellent transparency is obtained.

【0022】本発明の分子内に水酸基を有する脂肪族と
多塩基酸とから構成されるエステルのPET−G樹脂に
対する添加量は、PET−G樹脂100質量部に対し
0.1〜3.0質量部の範囲が適当である。添加量が
0.1質量部より少ないとカレンダーロール表面への樹
脂の粘着が十分に改善されず、添加量が3.0質量部よ
り多いと製品の透明性低下などが生じる場合がある。
The amount of the ester of the present invention composed of an aliphatic group having a hydroxyl group in the molecule and a polybasic acid, relative to the PET-G resin, of 0.1 to 3.0 with respect to 100 parts by mass of the PET-G resin. A range of parts by weight is appropriate. If the addition amount is less than 0.1 part by mass, the adhesion of the resin to the surface of the calender roll is not sufficiently improved, and if the addition amount is more than 3.0 parts by mass, the transparency of the product may be lowered.

【0023】本発明による分子内に水酸基を有する脂肪
族化合物と多塩基酸とから構成されるエステルのPET
−G樹脂への配合方法は、これらを均一に混合できる方
法であれば特に制限はなく、例えば、バンバリーミキサ
ー、加熱ロール等の各種混合機械による混合が使用でき
る。
PET of ester composed of an aliphatic compound having a hydroxyl group in the molecule and a polybasic acid according to the present invention
The method of compounding with -G resin is not particularly limited as long as they can be uniformly mixed. For example, mixing with various mixing machines such as a Banbury mixer and a heating roll can be used.

【0024】[0024]

【実施例】以下、実施例をもって本発明を説明するが、
本発明はこれらの実施例に限定されるものではない。
Hereinafter, the present invention will be described with reference to Examples.
The present invention is not limited to these examples.

【0025】<供試試料> 1.グリセリンコハク酸ラウリン酸エステル グリセリンモノラウレート[理研ビタミン社製蒸留モノ
グリセライド:リケマールM−300]の1モルと無水
コハク酸1モルとを公知の方法によりエステル化反応し
て得た。
<Test Sample> Glycerin succinate laurate ester 1 mol of glycerin monolaurate [distilled monoglyceride: RIQUEMAL M-300 manufactured by Riken Vitamin Co., Ltd.] and 1 mol of succinic anhydride were esterified by a known method.

【0026】2.グリセリンコハク酸ステアリン酸エス
テル グリセリンモノステアレート[理研ビタミン社製蒸留モ
ノグリセライド:リケマールS−100]の1モルと無
水コハク酸1モルとを公知の方法によりエステル化反応
して得た。
2. Glycerin succinate stearic acid ester It was obtained by subjecting 1 mol of glycerin monostearate [distilled monoglyceride: Richemal S-100 manufactured by Riken Vitamin Co., Ltd.] to 1 mol of succinic anhydride by a known method.

【0027】3.グリセリンコハク酸ベヘン酸エステル グリセリンモノベヘネート[理研ビタミン社製蒸留モノ
グリセライド:リケマールB−100]の1モルと無水
コハク酸1モルとを公知の方法でエステル化反応して得
た。
3. Glycerin Succinic Acid Behenic Acid Ester was obtained by subjecting 1 mol of glycerin monobehenate [distilled monoglyceride: Richemal B-100 manufactured by Riken Vitamin Co., Ltd.] to 1 mol of succinic anhydride by a known method.

【0028】4.グリセリンクエン酸ラウリン酸エステ
ル 上記グリセリンモノラウレート1モルとクエン酸1モル
とを公知の方法によりエステル化反応して得た。
4. Glycerin citrate laurate Ester was obtained by subjecting 1 mol of glycerin monolaurate and 1 mol of citric acid to an esterification reaction by a known method.

【0029】5.グリセリンクエン酸ステアリン酸エス
テル 上記グリセリンモノステアレート1モルとクエン酸1モ
ルとを公知の方法によりエステル化反応して得た。
5. Glycerin citrate stearic acid ester It was obtained by subjecting 1 mol of glycerin monostearate and 1 mol of citric acid to an esterification reaction by a known method.

【0030】6.グリセリンクエン酸ベヘン酸エステル 上記グリセリンモノベヘネート1モルとクエン酸1モル
とを公知の方法によりエステル化反応して得た。
6. Glycerin citrate behenate Ester was obtained by subjecting 1 mol of glycerin monobehenate and 1 mol of citric acid to an esterification reaction by a known method.

【0031】7.クエン酸ステアリル クエン酸1モルとステアリルアルコール[花王社製カル
コール8688]2モルとを公知の方法によりエステル
化反応して得た。
7. Stearyl citrate 1 mol of citric acid and 2 mol of stearyl alcohol [Kalcol 8688 manufactured by Kao Corporation] were esterified by a known method.

【0032】8.ポリエチレンワックス[三井石油化学
工業社製HIWAX200P]
8. Polyethylene wax [HIWAX200P manufactured by Mitsui Petrochemical Industries, Ltd.]

【0033】9.ステアリン酸[日本油脂社製桜牛脂ス
テアリン酸]
9. Stearic acid [Sakura beef stearic acid manufactured by NOF Corporation]

【0034】<試験及び評価>PET−G樹脂[EAS
TMAN CHEMICAL社製EASTER PET
−G6763]100質量部に対し試験試料の所定量
(質量部)を配合し、二軸押出し機により混練を行った
後、ペレット化した。得られたペレットを155℃に加
熱した8インチロールで5分間混練し、厚さ2mmのシ
ートに成形し、成形時のロール剥離性を観察評価した。
得られたシートを180℃、130Mpaで5分間プレ
スして5mm厚のプレスシートを作成し肉眼により透明
性を評価した。但し、評価は下記の基準によった。
<Tests and Evaluations> PET-G resin [EAS
EASTER PET manufactured by TMAN CHEMICAL
-G6763] A predetermined amount (parts by mass) of the test sample was blended with 100 parts by mass, kneaded by a twin-screw extruder, and then pelletized. The obtained pellets were kneaded with an 8-inch roll heated to 155 ° C. for 5 minutes, formed into a sheet having a thickness of 2 mm, and the roll releasability during the formation was observed and evaluated.
The obtained sheet was pressed at 180 ° C. and 130 MPa for 5 minutes to prepare a 5 mm-thick pressed sheet, and the transparency was evaluated with the naked eye. However, the evaluation was based on the following criteria.

【0035】(剥離性) ○:ロールに粘着することなくスムースに剥がれる △:ロールにやや粘着する ×:ロールに粘着し剥がれが悪い(Releasability) :: Smooth peeling without sticking to the roll △: Slightly sticking to the roll ×: Sticking to the roll and poor peeling

【0036】(透明性) ○:透明性良好 △:透明性やや不良 ×:透明性不良(Transparency) :: Good transparency Δ: Slightly poor transparency ×: Poor transparency

【0037】[0037]

【表1】 [Table 1]

【0038】[0038]

【発明の効果】本発明の改良剤を配合することにより、
良好なカレンダー加工性が得られ、かつ、透明性の優れ
たPET−G加工製品が得られる。
By incorporating the improver of the present invention,
Good calendering properties are obtained, and a PET-G processed product with excellent transparency is obtained.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】分子内に水酸基を有する脂肪族化合物と多
塩基酸とから構成されるエステルであり、当該エステル
1分子当たり少なくとも1個の遊離カルボキシル基が残
存するエステル1種又は2種以上の混合物を主成分とす
ることを特徴とするPET−G樹脂用加工性改良剤。
1. An ester comprising an aliphatic compound having a hydroxyl group in a molecule and a polybasic acid, wherein at least one free carboxyl group per ester molecule has at least one free carboxyl group remaining. A processability improver for a PET-G resin, comprising a mixture as a main component.
【請求項2】分子内に水酸基を有する脂肪族化合物が、
高級脂肪族1価アルコール、又は炭素数2〜6の多価ア
ルコール及び/又はそれらの重縮合物と高級脂肪酸との
部分エステルであることを特徴とする請求項1に記載の
PET−G樹脂用加工性改良剤。
2. An aliphatic compound having a hydroxyl group in the molecule,
2. The PET-G resin according to claim 1, which is a partial ester of a higher aliphatic monohydric alcohol or a polyhydric alcohol having 2 to 6 carbon atoms and / or a polycondensate thereof and a higher fatty acid. Processability improver.
【請求項3】多塩基酸が脂肪族ジカルボン酸又はトリカ
ルボン酸であることを特徴とする請求項1又は2に記載
のPET−G樹脂用加工性改良剤。
3. The processability improver for a PET-G resin according to claim 1, wherein the polybasic acid is an aliphatic dicarboxylic acid or a tricarboxylic acid.
【請求項4】請求項1、2又は3に記載の加工性改良剤
を含有することを特徴とするPET−G樹脂組成物。
4. A PET-G resin composition comprising the processability improver according to claim 1, 2 or 3.
JP2000238259A 2000-08-07 2000-08-07 PET-G resin composition and method for improving molding process Expired - Fee Related JP4633892B2 (en)

Priority Applications (1)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111073234A (en) * 2019-12-30 2020-04-28 浙江新力新材料股份有限公司 Heat-resistant flame-retardant PET composite material, preparation method thereof and application thereof in preparation of patch board

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JPH05295241A (en) * 1992-04-21 1993-11-09 Denki Kagaku Kogyo Kk Polyester resin composition
JPH07292223A (en) * 1994-04-22 1995-11-07 Dainippon Ink & Chem Inc Ester plasticizer for polyester resin and resin composition containing the same
JPH0820712A (en) * 1994-07-08 1996-01-23 Teijin Ltd Polybutylene terephthalate resin composition
JPH10316805A (en) * 1997-05-19 1998-12-02 Asahi Chem Ind Co Ltd Composition for calendering
JPH11343353A (en) * 1998-03-30 1999-12-14 Sumitomo Bakelite Co Ltd Polyester resin sheet and its preparation
JP2000086811A (en) * 1998-09-11 2000-03-28 Riken Vitamin Co Ltd Processing modifier for thermoplastic resin and thermoplastic resin composition

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JPS5365354A (en) * 1976-11-23 1978-06-10 Bayer Ag Rapidly crystallizable polyester composition
JPS62197446A (en) * 1986-02-26 1987-09-01 Idemitsu Petrochem Co Ltd Polyester resin composition
JPH05295241A (en) * 1992-04-21 1993-11-09 Denki Kagaku Kogyo Kk Polyester resin composition
JPH07292223A (en) * 1994-04-22 1995-11-07 Dainippon Ink & Chem Inc Ester plasticizer for polyester resin and resin composition containing the same
JPH0820712A (en) * 1994-07-08 1996-01-23 Teijin Ltd Polybutylene terephthalate resin composition
JPH10316805A (en) * 1997-05-19 1998-12-02 Asahi Chem Ind Co Ltd Composition for calendering
JPH11343353A (en) * 1998-03-30 1999-12-14 Sumitomo Bakelite Co Ltd Polyester resin sheet and its preparation
JP2000086811A (en) * 1998-09-11 2000-03-28 Riken Vitamin Co Ltd Processing modifier for thermoplastic resin and thermoplastic resin composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111073234A (en) * 2019-12-30 2020-04-28 浙江新力新材料股份有限公司 Heat-resistant flame-retardant PET composite material, preparation method thereof and application thereof in preparation of patch board
CN111073234B (en) * 2019-12-30 2022-04-08 浙江新力新材料股份有限公司 Heat-resistant flame-retardant PET composite material, preparation method thereof and application thereof in preparation of patch board

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