JPH06107917A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPH06107917A
JPH06107917A JP26349192A JP26349192A JPH06107917A JP H06107917 A JPH06107917 A JP H06107917A JP 26349192 A JP26349192 A JP 26349192A JP 26349192 A JP26349192 A JP 26349192A JP H06107917 A JPH06107917 A JP H06107917A
Authority
JP
Japan
Prior art keywords
acid
resin composition
titanium oxide
pbn
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
Application number
JP26349192A
Other languages
Japanese (ja)
Inventor
Takeshi Kojima
健 小嶋
Toshio Hatayama
敏雄 畑山
Akira Shimoma
昌 下間
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 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 Ltd filed Critical Teijin Ltd
Priority to JP26349192A priority Critical patent/JPH06107917A/en
Publication of JPH06107917A publication Critical patent/JPH06107917A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide a polybutylene 2,6-naphthalene dicarboxylate excellent in light resistance. CONSTITUTION:The resin composition is obtained by adding 0.5-10wt.% of titanium oxide to polybutylene 2,6-naphthalene dicarboxylate. The resin composition has good light resistance, and can especially prevent its UV light deterioration.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はポリブチレン―2,6―
ナフタレンジカルボキシレート(以下、PBN又はポリ
ブチレンナフタレートと略記する)の耐光性の改良に係
わる。
FIELD OF THE INVENTION The present invention relates to polybutylene-2,6-
It relates to improvement of light resistance of naphthalene dicarboxylate (hereinafter abbreviated as PBN or polybutylene naphthalate).

【0002】[0002]

【従来の技術】ポリブチレンナフタレートは耐熱性や機
械的強度等に優れる樹脂であり、電気・電子部品、自動
車部品或は機械部品等の広い利用分野があると言われて
いる。
2. Description of the Related Art Polybutylene naphthalate is a resin having excellent heat resistance and mechanical strength and is said to have a wide range of fields of use such as electric / electronic parts, automobile parts or mechanical parts.

【0003】しかるに、PBNは耐光性が必ずしも優れ
ていない。従来技術では研究開発が殆どなされていなか
ったので、PBNに関する技術蓄積がなく、耐光性を向
上せしめる手段等は全く知られていなかった。
However, PBN is not always excellent in light resistance. Since almost no research and development has been carried out in the prior art, there is no accumulated technology regarding PBN and no means for improving light resistance has been known.

【0004】本発明者らの研究によると、PBNは光、
特に紫外線に曝露されると変色しやすい傾向があること
が判った。そこで、この問題を解決すべく、鋭意研究を
進めた結果、酸化チタンを特定量配合したPBNは、意
外にも耐紫外線劣化性が良好であることを知見し、本発
明に到達した。
According to the research conducted by the present inventors, PBN is light,
It has been found that there is a tendency for discoloration to occur particularly when exposed to ultraviolet light. Then, as a result of earnestly researching in order to solve this problem, it was found that PBN containing a specific amount of titanium oxide has unexpectedly good resistance to ultraviolet ray deterioration, and arrived at the present invention.

【0005】[0005]

【発明の構成】本発明は、PBNに対し、酸化チタンを
0.5〜10重量%配合したものである。
According to the present invention, titanium oxide is added to PBN in an amount of 0.5 to 10% by weight.

【0006】以下本発明を詳述する。The present invention will be described in detail below.

【0007】本発明に用いるポリブチレンナフタレート
とは、ナフタレンジカルボン酸、好ましくはナフタレン
―2,6―ジカルボン酸を主たる酸成分とし、1,4―
ブタンジオールを主たるグリコール成分とするポリエス
テル、即ち繰り返し単位の全部または大部分(通常90
モル%以上、好ましくは95モル%以上)がブチレンナ
フタレートであるポリエステルである。
The polybutylene naphthalate used in the present invention comprises naphthalene dicarboxylic acid, preferably naphthalene-2,6-dicarboxylic acid as a main acid component, and 1,4-
Polyester containing butanediol as a main glycol component, that is, all or most of repeating units (usually 90
A polyester in which butylene naphthalate is used in an amount of not less than mol%, preferably not less than 95 mol%.

【0008】またこのポリエステルには物性を損なわな
い範囲で、次の成分の共重合が可能である。即ち、酸成
分としては、ナフタレンジカルボン酸以外の芳香族ジカ
ルボン酸、例えばフタル酸、イソフタル酸、テレフタル
酸、ジフェニルジカルボン酸、ジフェニルエーテルジカ
ルボン酸、ジフェノキシエタンジカルボン酸、ジフェニ
ルメタンジカルボン酸、ジフェニルケトンジカルボン
酸、ジフェニルスルフィドジカルボン酸、ジフェニルス
ルフォンジカルボン酸、脂肪族ジカルボン酸、例えばコ
ハク酸、アジピン酸、セバシン酸、脂環族ジカルボン
酸、例えばシクロヘキサンジカルボン酸、テトラリンジ
カルボン酸、デカリンジカルボン酸等が例示される。
Further, this polyester can be copolymerized with the following components as long as the physical properties are not impaired. That is, as the acid component, an aromatic dicarboxylic acid other than naphthalenedicarboxylic acid, for example, phthalic acid, isophthalic acid, terephthalic acid, diphenyldicarboxylic acid, diphenyletherdicarboxylic acid, diphenoxyethanedicarboxylic acid, diphenylmethanedicarboxylic acid, diphenylketonedicarboxylic acid, Examples thereof include diphenyl sulfide dicarboxylic acid, diphenyl sulfone dicarboxylic acid, aliphatic dicarboxylic acid such as succinic acid, adipic acid, sebacic acid, alicyclic dicarboxylic acid such as cyclohexanedicarboxylic acid, tetralindicarboxylic acid and decalindicarboxylic acid.

【0009】グリコール成分としてはエチレングリコー
ル、プロピレングリコール、トリメチレングリコール、
ペンタメチレングリコール、ヘキサメチレングリコー
ル、オクタメチレングリコール、ネオペンチルグリコー
ル、シクロヘキサンジメタノール、キシリレングリコー
ル、ジエチレングリコール、ポリエチレングリコール、
ビスフェノールA、カテコール、レゾルシノール、ハイ
ドロキノン、ジヒドロキシジフェニル、ジヒドロキシジ
フェニルエーテル、ジヒドロキシジフェニルメタン、ジ
ヒドロキシジフェニルケトン、ジヒドロキシジフェニル
スルフィド、ジヒドロキシジフェニルスルフォン等が例
示される。
As the glycol component, ethylene glycol, propylene glycol, trimethylene glycol,
Pentamethylene glycol, hexamethylene glycol, octamethylene glycol, neopentyl glycol, cyclohexanedimethanol, xylylene glycol, diethylene glycol, polyethylene glycol,
Examples include bisphenol A, catechol, resorcinol, hydroquinone, dihydroxydiphenyl, dihydroxydiphenyl ether, dihydroxydiphenylmethane, dihydroxydiphenylketone, dihydroxydiphenylsulfide, dihydroxydiphenylsulfone and the like.

【0010】オキシカルボン酸成分としては、オキシ安
息香酸、ヒドロキシナフトエ酸、ヒドロキシジフェニル
カルボン酸、ω―ヒドロキシカプロン酸等が例示され
る。
Examples of the oxycarboxylic acid component include oxybenzoic acid, hydroxynaphthoic acid, hydroxydiphenylcarboxylic acid and ω-hydroxycaproic acid.

【0011】また、ポリエステルが実質的に成形性能を
失わない範囲で3官能以上の化合物、例えばグリセリ
ン、トリメチルプロパン、ペンタエリスリトール、トリ
メリット酸、ピロメリット酸等を共重合して良い。
Further, trifunctional or higher functional compounds such as glycerin, trimethylpropane, pentaerythritol, trimellitic acid and pyromellitic acid may be copolymerized as long as the polyester does not substantially lose the molding performance.

【0012】かかるポリエステルは、ナフタレンジカル
ボン酸及び/またはその機能的誘導体とブチレングリコ
ール及び/またはその機能的誘導体とを、従来公知の芳
香族ポリエステル製造法を用いて重縮合させて得られ
る。
Such a polyester can be obtained by polycondensing naphthalenedicarboxylic acid and / or a functional derivative thereof and butylene glycol and / or a functional derivative thereof by a conventionally known method for producing an aromatic polyester.

【0013】本発明に用いる酸化チタンについては、ル
チル型やアナターゼ型などタイプはいずれでもよく、ま
た平均粒径については得られる成形品の外観等に悪影響
がなければ特に限定されない。PBNに酸化チタンを配
合する方法については、例えば単軸、二軸などの押出機
にPBNと酸化チタンを供給して混練する方法や、PB
N重縮合の前又は重合中に酸化チタンを配合する方法が
ある。
The titanium oxide used in the present invention may be of any type such as rutile type or anatase type, and the average particle size is not particularly limited as long as it does not adversely affect the appearance of the obtained molded product. Regarding the method of blending titanium oxide with PBN, for example, a method of feeding PBN and titanium oxide to an extruder such as a single-screw or twin-screw extruder and kneading,
There is a method of adding titanium oxide before N-polycondensation or during polymerization.

【0014】酸化チタンの添加量は、PBN100重量
部に対し、0.5〜10重量部である。0.5重量部よ
り少ないと変色抑制の効果が少い。また10重量部を超
えると、引張強度が低下し、エンジニアリングプラスチ
ックスとしての用途目的に適さなくなる。
The amount of titanium oxide added is 0.5 to 10 parts by weight based on 100 parts by weight of PBN. If it is less than 0.5 part by weight, the effect of suppressing discoloration is small. On the other hand, if it exceeds 10 parts by weight, the tensile strength is lowered and it becomes unsuitable for the purpose of use as engineering plastics.

【0015】本発明のPBNには、酸化チタンの他に、
その用途目的に応じて各種添加剤、例えば繊維状、板
状、粉粒状などの各形状を有する強化剤、安定剤、着色
剤、離型剤、帯電防止剤、結晶化促進剤、結晶核剤、充
填剤、衝撃改良剤、難燃剤、難燃助剤等を添加でき、と
くに紫外線吸収剤は酸化チタン添加の効果を強化するの
で好ましい。
In the PBN of the present invention, in addition to titanium oxide,
Various additives depending on the purpose of use, for example, reinforcing agents having various shapes such as fibrous, plate-like, powdery, etc., stabilizers, colorants, release agents, antistatic agents, crystallization accelerators, crystal nucleating agents. , A filler, an impact modifier, a flame retardant, a flame retardant aid, etc. can be added, and an ultraviolet absorber is particularly preferable because it enhances the effect of adding titanium oxide.

【0016】本発明のPBNと酸化チタンよりなる組成
物から成形品を得る方法としては射出成形法が最も望ま
しいが、そのほかにも押出成形法、圧縮成形法、トラン
スファー成形法、ブロー成形法などの公知の成形方法を
取ることができるほか、これらの成形方法によって得ら
れた成形品にさらに切削、溶着、接着、接合、曲げ、メ
ッキ蒸着、印刷、塗装などの二次加工を施すことも可能
である。
The injection molding method is the most preferable method for obtaining a molded product from the composition of PBN and titanium oxide of the present invention, but in addition to this, an extrusion molding method, a compression molding method, a transfer molding method, a blow molding method and the like. In addition to the known molding methods, it is also possible to subject the molded products obtained by these molding methods to secondary processing such as cutting, welding, bonding, joining, bending, plating vapor deposition, printing and painting. is there.

【0017】[0017]

【実施例】以下に実施例を挙げて本発明を補説する。EXAMPLES The present invention will be supplemented with examples below.

【0018】主な特性の測定方法は以下の通りである。The main characteristic measuring methods are as follows.

【0019】耐光性試験 スガ試験機(株)製サンシャインスーパーロングライフ
ウェザーメーター(WEL―SUN―HCH)に樹脂試
験片を装着し、カーボンアークによる紫外線を500時
間照射した。
Light resistance test A resin test piece was mounted on a Sunshine Super Long Life Weather Meter (WEL-SUN-HCH) manufactured by Suga Test Instruments Co., Ltd. and irradiated with ultraviolet rays by carbon arc for 500 hours.

【0020】次いで該試験片の色相をミノルタ(株)製
の色彩色差計(CR―100)にて黄色度(YI)を測
定し、紫外線照射前のYIとの差をΔYIとして変色の
度合いとした。
Next, the hue of the test piece was measured for yellowness (YI) with a color difference meter (CR-100) manufactured by Minolta Co., Ltd. did.

【0021】樹脂の調製 実施例及び比較例にて用いた樹脂組成物は以下の如くし
て得た。
Preparation of Resin The resin compositions used in Examples and Comparative Examples were obtained as follows.

【0022】オルトクロロフェノール中にて測定した固
有粘度数が0.85のPBNと平均粒径0.25μmの
ルチル型酸化チタンを、それぞれの所定量、単軸押出機
に供給して、溶融混練してペレット状の樹脂組成物を得
た。
PBN having an intrinsic viscosity of 0.85 measured in ortho-chlorophenol and rutile-type titanium oxide having an average particle size of 0.25 μm were fed to a single-screw extruder in predetermined amounts and melt-kneaded. A pelletized resin composition was obtained.

【0023】かくして得られた樹脂組成物のペレットを
射出成形機を用いて滑らかな表面の平板(50mm径×2
mm厚さ)を成形し、紫外線照射試験用の試料とした。
A pellet having a smooth surface (50 mm diameter × 2) was obtained from the pellet of the resin composition thus obtained by using an injection molding machine.
(mm thickness) was molded and used as a sample for an ultraviolet irradiation test.

【0024】樹脂組成物の構成比並びに紫外線照射試験
の結果を表1にまとめた。
The composition ratio of the resin composition and the result of the ultraviolet irradiation test are summarized in Table 1.

【0025】[0025]

【表1】 [Table 1]

【0026】YIの値は、JIS Z8701―195
8に規定されたX、Y、Z値を基に式、YI=100
(1.28X―1.06Z)/Yを用いて算出した。
The value of YI is JIS Z8701-195.
Formula based on the X, Y, and Z values defined in 8, YI = 100
It was calculated using (1.28X-1.06Z) / Y.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ポリブチレンナフタレート100重量部
に対し、酸化チタン0.5〜10重量部を配合してなる
樹脂組成物。
1. A resin composition comprising 0.5 to 10 parts by weight of titanium oxide mixed with 100 parts by weight of polybutylene naphthalate.
JP26349192A 1992-10-01 1992-10-01 Resin composition Pending JPH06107917A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26349192A JPH06107917A (en) 1992-10-01 1992-10-01 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26349192A JPH06107917A (en) 1992-10-01 1992-10-01 Resin composition

Publications (1)

Publication Number Publication Date
JPH06107917A true JPH06107917A (en) 1994-04-19

Family

ID=17390260

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26349192A Pending JPH06107917A (en) 1992-10-01 1992-10-01 Resin composition

Country Status (1)

Country Link
JP (1) JPH06107917A (en)

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