JPS58206663A - Polyester composition - Google Patents

Polyester composition

Info

Publication number
JPS58206663A
JPS58206663A JP8933682A JP8933682A JPS58206663A JP S58206663 A JPS58206663 A JP S58206663A JP 8933682 A JP8933682 A JP 8933682A JP 8933682 A JP8933682 A JP 8933682A JP S58206663 A JPS58206663 A JP S58206663A
Authority
JP
Japan
Prior art keywords
polyester
inorganic filler
average particle
amorphous
spherical inorganic
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
JP8933682A
Other languages
Japanese (ja)
Other versions
JPH0525903B2 (en
Inventor
Shigeo Kobayashi
重夫 小林
Kiyoji Nanbu
喜代治 南部
Nori Yoshihara
法 葭原
Yukio Goto
行雄 五藤
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.)
Toyobo Co Ltd
Original Assignee
Toyobo 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 Toyobo Co Ltd filed Critical Toyobo Co Ltd
Priority to JP8933682A priority Critical patent/JPS58206663A/en
Publication of JPS58206663A publication Critical patent/JPS58206663A/en
Publication of JPH0525903B2 publication Critical patent/JPH0525903B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:The titled composition having extremely improved warpage deformation such as inner warp, twist of a box or channel shaped molded article, improved molding properties, etc., obtained by blending a polyester with an amorphous or spherical inorganic filler together with a fibrous reinforcing agent and a nucleating agent for crystallization. CONSTITUTION:30-72wt% polyester (preferably >=0.4 intrinsic viscosity) having at least >=80mol% ethylene terephthalate repeating unit is blended with 8- 50wt% fibrous reinforcing agent (preferably glass fibers having <=30mu diameters and 0.1-5mm. length), 19.8-60wt% amorphous or spherical inorganic filler (especially wollastonite) having 2-15mu average particle diameters, and 0.2-5wt% nucleating agent for crystallization having <=10mu average particle diameter (preferably 0.1-5mu) selected from talc, mica, titanium oxide, and carbon black in a molten state. The addition of an ester of a higher fatty acid and an alcohol is preferably to improve releasability, surface gloss of a molded article, etc.

Description

【発明の詳細な説明】 本発明はポリエステル組成物に関するものであり1更に
詐L〈は特に箱型やチャンネル型成形品での内シリ1ネ
ジレ等のソリ変形の改良されたポリエステル組成物を捉
供するにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polyester composition, and 1 further relates to a polyester composition which is particularly effective in preventing warp deformation such as internal warpage and twisting in box-shaped or channel-shaped molded products. It is to serve.

ポリエチレンテレフタレートは機械的性質、 mt気的
性貿)熱的性*、耐薬品性に優れ1フイルムその他の成
形用材料として有用である。そして成形品として使用す
る場合−%剛性を改良するためガラス11タルク等の補
強剤によって強化した組成物が用いられることは良く知
られている。しかしながら、かかる強化組成物から特に
箱型やチャンネル型の成形品を成形するときは成形品が
内シリ、ネジレ等のソリ変形を生じ易い欠点を有してい
る。
Polyethylene terephthalate has excellent mechanical properties, thermal properties*, and chemical resistance, and is useful as a material for forming films and other materials. It is well known that when used as a molded article, a composition reinforced with a reinforcing agent such as glass 11 talc is used to improve the rigidity. However, when molding a box-shaped or channel-shaped molded article from such a reinforced composition, the molded article has a disadvantage that it is susceptible to warping deformation such as internal warping and twisting.

本姥明者等は強化組成物であって為しかもソリ変形の着
しく改善された成形材料を得る−べく鋭意研究の結果、
本発明のぎりエステル組成物に到達した。
As a result of intensive research, Akira Motoba et al. aimed to obtain a molding material that is a reinforced composition and has improved warp deformation.
An ester composition according to the present invention has been achieved.

すなわち、本発明は臣チレンテレ7タレート保返し箪位
が少なくとも80モル%以上のポリエステル30〜72
重jIt%1繊維状強化剤8〜501izm%1平均粒
径2〜15μの無定形またVi球状の無機充填剤19.
8〜60重蓋%およびタルク為マイカ、酸化チタンおよ
びカーボンブラックの群から選ばれた少なくとも1柚の
平均粒径が10μ以下の結晶化核剤0,2〜5重J11
%からなることを待機とするポリエステル組成物である
That is, the present invention is a polyester containing at least 80 mol % of polyester 30 to 72 mol%.
Heavy jIt%1 Fibrous reinforcing agent 8-501izm%1 Amorphous or Vi spherical inorganic filler with an average particle size of 2-15μ19.
A crystallization nucleating agent with an average particle size of 8 to 60% and talc, mica, titanium oxide, and carbon black with an average particle size of 10μ or less J11
% of polyester composition.

本発明によるポリエステル組成物は、ことに箱型やチャ
ンネル型成形品での内シリ1ネジレ等のソリ変形が著し
く小さい特長を有する。また)機械的特性島成形性等も
優れるなど多くの特長を有している。
The polyester composition according to the present invention has a feature that warping deformation such as inner warp twisting in box-shaped or channel-shaped molded products is extremely small. It also has many features such as excellent mechanical properties and island formability.

本発明で使用するポリエステルはポリエチレンテレフタ
レートもしくけ少なくとも80モル%以上A好ましくは
90モル%以上のエチレンテレフタレート繰返し単位を
含む共真合ポリエステルである。共東合成分としては従
来公知の顔成分および/またはグリコール成分が使用で
きる。すなゎち、共重合成分として#−tまたとえばイ
ソフタル酸、ナフタレン1.4−またf′i2.6−ジ
カルボン酸、ジフェニルエーテル4,4−ジカルボン酸
、アジピン敞1セバシン版のような酸成分、プロピレン
グリコール1ブチレングリコール)ジエチレングリコー
ル1ネオペンチルグリコール、シクロヘキサンジメタツ
ール、2,2−ビス(4−ヒドロキシフェニル)プロパ
ンのようなグリコール成分sp−オキシ安息1トp−ヒ
ドロキシェトギシ安息香酸のようなオキシ酸等が挙げら
れる。なお1ポリエステルはフェノール/テトラクロロ
エタン混合溶媒(6/4東蓋比)浴液により30℃で測
定して求めた固有粘度が0.4以上であることが好まし
く、更には0.5以上であることが特に好ましい。また
ポリエステルは成形性を゛損わない範囲で一部分岐して
いてもよい。固有粘度の異なる2椙以上のポリエステル
のブレンドであってもよい。
The polyester used in the present invention is a copolymerized polyester containing polyethylene terephthalate repeating units of at least 80 mol % or more, preferably 90 mol % or more. As Kyodosei ingredients, conventionally known facial ingredients and/or glycol ingredients can be used. In other words, acid components such as #-t as copolymerization components, such as isophthalic acid, naphthalene 1,4- or f'i2,6-dicarboxylic acid, diphenyl ether 4,4-dicarboxylic acid, and adipine 1 sebacin version. Glycol components such as , propylene glycol 1 butylene glycol) diethylene glycol 1 neopentyl glycol, cyclohexane dimetatool, 2,2-bis(4-hydroxyphenyl)propane sp-oxybenzoate 1 topyl p-hydroxyethoxybenzoic acid Examples include oxyacids such as Note that the polyester preferably has an intrinsic viscosity of 0.4 or more, more preferably 0.5 or more, as measured at 30°C using a phenol/tetrachloroethane mixed solvent (6/4 ratio) bath solution. It is particularly preferable. Further, the polyester may be partially branched to the extent that moldability is not impaired. It may also be a blend of two or more polyesters having different intrinsic viscosities.

本発明において用いられる繊維状強化剤としては、たと
えばガラス繊維1カーボンまたはグラファイト繊維1炭
化金属繊維1窒化金MIa維1炭化珪素繊維1各梱ホイ
スカー1硬化フェノールホルマリン繊維)アラミド縁組
等が例示される。しかし1特に好ましいのけガラス繊維
である。繊維の直径は30μ以下であり九好ましくは1
〜10μである。繊維長は繊維の41!類、添加皺等に
よっても幾なるが)平均で通幇0.1〜5m程度であり
1好ましくは主体が0.1−0.6 Mの繊維である。
Examples of the fibrous reinforcing agent used in the present invention include glass fiber 1 carbon or graphite fiber 1 metal carbide fiber 1 gold nitride MIa fiber 1 silicon carbide fiber 1 each bale whisker 1 hardened phenol-formalin fiber) aramid bond, etc. . However, one particularly preferred is the glass fiber. The diameter of the fiber is 30μ or less, preferably 1
~10μ. The fiber length is 41! On average, the diameter is about 0.1 to 5 m (although it varies depending on the type, added wrinkles, etc.), and preferably the main fiber is 0.1 to 0.6 M fiber.

短かすぎるとタフネスが低下し、補強効果が小さくなる
。繊維状強化剤はポリエステル中への分散性またはポリ
エステルとの接着性を改良するための処理剤またとえば
ガラス繊維ではシラン糸カップラー、チタン系カップラ
ー等で処理するのが好ましい。
If it is too short, the toughness will decrease and the reinforcing effect will decrease. The fibrous reinforcing agent is preferably treated with a treatment agent such as a silane yarn coupler, a titanium coupler, etc. in the case of glass fiber to improve its dispersibility in polyester or its adhesion to polyester.

本発明において用いられる平均粒径2〜15μの無定形
または球状の無機充填剤としてはワラストナイト、炭酸
カルシウム)ガラス粉末等か例ボされるが一部特にワラ
ストナイトが好ましい。該充填剤もまたポリエステル中
への分散性やポリエステルとの接着性を改良するための
表面処理をkしてもよい。
Examples of the amorphous or spherical inorganic filler having an average particle diameter of 2 to 15 microns used in the present invention include wollastonite, calcium carbonate) glass powder, etc., and wollastonite is particularly preferred. The filler may also be subjected to surface treatment to improve its dispersibility in polyester and its adhesion to polyester.

従来、板状のタルク1マイカやガラスを配合した成形材
料eよ知られているか)′#i型成形尻で内シリやネジ
レ寺のソリ変形を生じる欠点を有している。このような
欠点を主として無定形または球状の無機充填剤の特定量
を配合することによって解決したのが本発明である。
Conventionally, a molding material e containing plate-shaped talc, mica, and glass has been known.) It has the disadvantage of causing internal warping and warping deformation at the end of the i-type molding. The present invention solves these drawbacks by mainly incorporating a specific amount of an amorphous or spherical inorganic filler.

更に本発明においては)成形性1衣面特性等を 。Furthermore, in the present invention) moldability 1 coating surface characteristics, etc.

改良するため平均粒径が10μ以下)特に好ましくは0
.1〜5μのタルク1マイカ−、酸化チタンAカーボン
ブラックから賄ばれた結晶化核剤が配合される。
In order to improve the average particle size (10 μ or less), particularly preferably
.. A crystallization nucleating agent comprised of 1 to 5 μm of talc, mica, and titanium oxide A carbon black is blended.

本発明のポリエステル組成物Vこおける上記成分の配合
′11j合はポリエステルが30〜72mm%1繊維状
強化剤が8〜50本m%、無機充填剤が19.8〜60
]k蓋%および結晶化核剤か0.2〜53kM%である
。繊維状強化剤が過少の場合は成形品の強度1剛性が不
充分であり、過多の場合は成形品の破断伸度が低下して
脆くなるはかコンパウンド困麺となる。また無機充填剤
が過少の場合はソリ変形態が大きく1また過多の場合は
成形時の流動性が低下し為成形品の破断伸度が低下して
タフネスが減少するほか表面特性も悪化する。更に結晶
化核剤が過小の場合は成形性や成形品の表圓特性が劣り
為過多の場合はソリ変形iが大きくなる欠点を生じる。
The composition of the above components in the polyester composition V of the present invention '11j is 30 to 72 mm% of polyester, 8 to 50 m% of fibrous reinforcing agent, and 19.8 to 60 m% of inorganic filler.
]k% and crystallization nucleating agent are 0.2 to 53kM%. If the amount of fibrous reinforcing agent is too small, the strength and rigidity of the molded product will be insufficient, and if it is too large, the elongation at break of the molded product will decrease, resulting in a brittle compound. In addition, if the inorganic filler is too small, warp deformation will be large, and if the inorganic filler is too large, the fluidity during molding will decrease, resulting in a decrease in the elongation at break of the molded product, resulting in a decrease in toughness and deterioration of the surface properties. Furthermore, if the amount of the crystallization nucleating agent is too small, the moldability and surface characteristics of the molded product will be poor, and if it is too large, the warp deformation i will become large.

本発明の組成物には離型性1成形品の表囲光沢等を改良
するため高級脂酸たとえば炭素数15〜50の脂肪酸と
アルコールとのエステル為該脂肪酸と周期律表第1A族
または第MA族金属との塩およびそれらの混合物を配合
す之ことが好ましい。
The composition of the present invention contains esters of higher fatty acids, such as fatty acids having 15 to 50 carbon atoms, and alcohols in order to improve surface gloss etc. of molded products. It is preferred to incorporate salts with MA group metals and mixtures thereof.

具体的にはステーアリン酸ナトリウム1ステアリン酸マ
グネシウム1ステアリン酸カルシウム、モンタン峡カル
シウム1モンクン酸エステル等が例示賂れる。
Specific examples include sodium stearate, magnesium stearate, calcium stearate, and calcium montan acid ester.

本発明の組成物には更に所望により有機結晶化促進剤た
とえばポリアルキレングリコール、ポリアルキレングリ
コールのモノまたはジエーテルもしくはモノまたはジエ
ステル、モノまたは多価アルコールの芳香族カルボン酸
エステル1安)#1.香酸の金属塩1ベンゾフエノン)
カルボ>g金m塩基含有ポリマー等1離燃剤たとえばハ
ロゲン化ビスフェノールの炭酸エステルノリゴマ−1ハ
ロゲン化ビスフェノールのシアヌル絃エステルオゴマー
等、絵燃助剤たとえばアンチモン化合物為架橋剤たとえ
ばグリコールジグリシジルエーテル1ポリアルキレング
リコールジグリシジルエーテル)ビスフェノールジグリ
シジルエーテル等)安定剤たとえば酸化防止剤、紫外巌
吸収剤、耐衝撃性改良剤たとえば芳香族ポリエステルポ
リエーテル癲性体1芳:&族ポリエステル脂肪族ポリエ
ステル弾性体、イオン性基または反応性基を導入したゴ
ム状g IJママ−)yI1色剤等の各柚添加剤を配合
することができる。また1本発明の要旨を逸脱しない量
およびat類の他の熱可塑性樹脂を更に追加配合しても
よい。
The compositions of the present invention may optionally further contain organic crystallization promoters such as polyalkylene glycols, mono- or diethers or mono- or diesters of polyalkylene glycols, aromatic carboxylic acid esters of mono- or polyhydric alcohols, and #1. Metal salts of aromatic acid (1 benzophenone)
Carbo>g Gold m Base-containing polymer etc. 1 Flame retardant such as carbonate ester oligomer of halogenated bisphenol 1 Cyanuric acid ester oligomer of halogenated bisphenol etc. Combustion aid such as antimony compound Crosslinking agent such as glycol diglycidyl ether 1 (polyalkylene glycol diglycidyl ether) bisphenol diglycidyl ether, etc.) Stabilizers such as antioxidants, ultraviolet absorbers, impact modifiers such as aromatic polyester polyether lepidic body 1 aromatic: & group polyester aliphatic polyester elastomer , rubber-like g IJ mama-) yI1 coloring agents into which ionic groups or reactive groups have been introduced, and other yuzu additives can be blended. Further, other thermoplastic resins such as AT may be additionally blended in an amount that does not depart from the gist of the present invention.

本発明の組成物の製造法としては)特に制限されるもの
ではなく任逮の方法で行われる。たとえばポリエステル
と他の全組成を予め混合して押出機によりコンパウンド
化する方法1ポリエステルと轍維状強化剤以外の全組成
を混合して押出機に投入し1その溶融物をガラス四−ビ
ング等の周囲に被筒して冷却した後1適当な長葛に切断
するいわゆる電線被楓法X繊維状強化剤および/または
充填剤等をポリエステルの重合段階または重合後添加し
た後1これに他の全組成を混合する方法\繊維状強化剤
配合ポリエステルと他の充填剤配合ポリエステルをブレ
ンドする方法等が挙けられる。
The method for producing the composition of the present invention is not particularly limited, and any method may be used. For example, a method in which polyester and all other components are mixed in advance and compounded using an extruder. 1. All components except the polyester and rutted fiber reinforcement are mixed and put into an extruder. 1. The molten material is poured into a glass 4-bing, etc. After cooling, the wire is cut into suitable lengths.The so-called electric wire wrapping method. Examples include a method of mixing the entire composition\a method of blending a fibrous reinforcing agent-containing polyester and another filler-containing polyester.

しかし1混合法島配合時期は必ずしもこれらに限定され
るものではない。
However, the mixing timing of the first mixing method is not necessarily limited to these.

かくして得られた組成物は高温金型成形ではもちろんの
こと1低温金型成形においてもすぐれた成形性と表面特
゛性の良好な成形品を与えることから各梱成形部品)シ
ート状物1管状物1槓層物容器等の成形に広く利用でき
るが1すぐれた耐ソリ性を考慮しなとき箱型やチャンネ
ル型成形品等の成形に特に好適である。低温金型成形品
は必要により後熱処理して加熱結晶化させ耐熱安定化す
ることができる。
The composition thus obtained provides molded products with excellent moldability and surface properties not only in high-temperature molding but also in low-temperature molding. It can be widely used for molding multi-layer containers, etc., but is particularly suitable for molding box-shaped or channel-shaped molded products when excellent warpage resistance is not taken into account. If necessary, the low-temperature molded product can be subjected to post-heat treatment to crystallize it and stabilize its heat resistance.

以下、実施例により本発明を説明する。なお、実施例中
における1%はムに%である。
The present invention will be explained below with reference to Examples. In addition, 1% in the examples is %.

実地例 ポリエチレンテレフタレート(同宿粘度0・60)と長
さ3闘、直径10μのガラスチョツプドストランド)平
均粒径3μのタルク(結晶核剤)および各種無機充填剤
を表1に示す割合でタンブルブレングー中で混合した。
Practical example Polyethylene terephthalate (viscosity 0.60), glass chopped strands with a length of 3 mm and a diameter of 10 μm), talc (crystal nucleating agent) with an average particle size of 3 μm, and various inorganic fillers were tumbled in the proportions shown in Table 1. Mixed in a blender.

次いで4011+3φベント式押出機のホッパーに投入
し為シリンダー7M度(ホッパー側から) 250−2
70−280°Cで溶融混練L1各組成のフンバウンド
チップを製造した。
Next, put it into the hopper of a 4011 + 3φ vent type extruder and use a cylinder of 7M degrees (from the hopper side) 250-2
Funbound chips of each composition were produced by melt-kneading L1 at 70-280°C.

得られたコンパウンドチップを120℃、4時間減圧乾
燥した後1射出成形機を使用してシリンダー % k2
70−265−270℃、金型温度120℃、射出保圧
時間15抄間A冷却時[司15秒間、射出圧力50に9
/C−で長辺70m57辺5C++am19さ20闘、
厚み2闘の第1図に示す形状の箱型を成形した0 得られた成形品を室温24時間放置したときの長辺側板
の最大内シリ寸法A(第2図を照)を測定し、内シリの
程度を求めた。
The obtained compound chips were dried at 120°C for 4 hours under reduced pressure and then molded into a cylinder using an injection molding machine.
70-265-270℃, mold temperature 120℃, injection pressure holding time 15 during paper cooling A [15 seconds, injection pressure 50 to 9
/C- long side 70m57 side 5C++am19sa20th,
A box-shaped product with a thickness of 2 mm and the shape shown in Figure 1 was molded.The resulting molded product was left at room temperature for 24 hours, and the maximum internal sill dimension A (see Figure 2) of the long side plate was measured. The degree of internal warping was determined.

その結果を第1表に示した。The results are shown in Table 1.

その時朱、本発明の組成物によりソリ変形の小さい\か
つすぐれた物性を有する成形品が得られた0
At that time, it was confirmed that a molded article with small warp deformation and excellent physical properties was obtained using the composition of the present invention.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は内シリを評価するため本発明をポリエステル組
成物から成形された箱型成形品の見取図である。また1
第2図は第1図に示した箱型成形品を’<渇24時間放
置した後の内シリの測定部位Aをボす説明図である。 特許出願人 東洋紡−株式会社
FIG. 1 is a sketch of a box-shaped molded product made from a polyester composition according to the present invention in order to evaluate internal wrinkles. Also 1
FIG. 2 is an explanatory diagram showing a measurement site A of internal shavings after the box-shaped molded product shown in FIG. 1 has been left for 24 hours. Patent applicant: Toyobo Co., Ltd.

Claims (1)

【特許請求の範囲】 L エチレンテレフタレート繰返し単位が少なくきも8
0モル%以上のポリエステル30〜72m蓋%S繊維状
強化剤8〜50本量%1平均粒径2〜lfiμの無定形
または球状の無機充填剤19.8〜60菖−%およびタ
ルク)マイカ1散化チタンおよびカーボンブラックの群
から適りれた少なくとも1槁の平均粒径が10μ以下の
結晶化核剤0.2〜5[1%からなることを特徴とする
ポリエステル組成物0 2 無定形または球状の無機充填剤がワラストナイト、
炭酸カルシウムおよびガラス粉末から趨ばれた少なくと
もl櫨である待鈴餉求の範囲第1項記載のポリエステル
組成物。 器 無定形または球状の無機充填剤がワラストナイトで
ある特許請求の範囲第2項記載のポリエステル組成物。
[Scope of Claims] L Low ethylene terephthalate repeating units 8
Polyester of 0 mol% or more 30-72 m Lid % S Fibrous reinforcement 8-50 % Weight 1 Amorphous or spherical inorganic filler with an average particle size of 2-lfiμ 19.8-60 Iris-% and talc) Mica A polyester composition comprising 0.2 to 5 [1%] of at least one crystallization nucleating agent selected from the group of monodispersed titanium and carbon black and having an average particle size of 10 μ or less. Wollastonite is a regular or spherical inorganic filler.
2. The polyester composition according to claim 1, which is at least one polyester blended with calcium carbonate and glass powder. The polyester composition according to claim 2, wherein the amorphous or spherical inorganic filler is wollastonite.
JP8933682A 1982-05-25 1982-05-25 Polyester composition Granted JPS58206663A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8933682A JPS58206663A (en) 1982-05-25 1982-05-25 Polyester composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8933682A JPS58206663A (en) 1982-05-25 1982-05-25 Polyester composition

Publications (2)

Publication Number Publication Date
JPS58206663A true JPS58206663A (en) 1983-12-01
JPH0525903B2 JPH0525903B2 (en) 1993-04-14

Family

ID=13967841

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8933682A Granted JPS58206663A (en) 1982-05-25 1982-05-25 Polyester composition

Country Status (1)

Country Link
JP (1) JPS58206663A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4711916A (en) * 1982-09-30 1987-12-08 Nippon Steel Corporation Inorganic filler dispersed-resin composition
JPS63120756A (en) * 1986-11-10 1988-05-25 Kuraray Co Ltd Filled resin composition
JPH01210452A (en) * 1988-02-18 1989-08-24 Idemitsu Petrochem Co Ltd Glass fiber-reinforced polyester resin composition
WO1995029134A1 (en) * 1994-04-25 1995-11-02 Minnesota Mining And Manufacturing Company Compositions comprising fused particulates and methods of making them
US6045913A (en) * 1995-11-01 2000-04-04 Minnesota Mining And Manufacturing Company At least partly fused particulates and methods of making them by flame fusion
US6254981B1 (en) 1995-11-02 2001-07-03 Minnesota Mining & Manufacturing Company Fused glassy particulates obtained by flame fusion
CN109561791A (en) * 2016-08-04 2019-04-02 住友化学株式会社 Resin combination is used in flameproof ware, the manufacturing method of flameproof ware and flameproof ware forming

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3404154B2 (en) 1994-09-27 2003-05-06 鐘淵化学工業株式会社 Flame retardant polyester resin composition

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53121843A (en) * 1977-04-01 1978-10-24 Polyplastics Kk Thermoplastic resin mold composition
JPS5458753A (en) * 1977-10-18 1979-05-11 Toyobo Co Ltd Polyester composition
JPS5474852A (en) * 1977-11-29 1979-06-15 Teijin Ltd Polyester resin composition
JPS5486548A (en) * 1977-12-23 1979-07-10 Mitsubishi Rayon Co Ltd Polyethylene terephthalate type composition
JPS54148833A (en) * 1978-05-15 1979-11-21 Toyobo Co Ltd Polyester composition

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53121843A (en) * 1977-04-01 1978-10-24 Polyplastics Kk Thermoplastic resin mold composition
JPS5458753A (en) * 1977-10-18 1979-05-11 Toyobo Co Ltd Polyester composition
JPS5474852A (en) * 1977-11-29 1979-06-15 Teijin Ltd Polyester resin composition
JPS5486548A (en) * 1977-12-23 1979-07-10 Mitsubishi Rayon Co Ltd Polyethylene terephthalate type composition
JPS54148833A (en) * 1978-05-15 1979-11-21 Toyobo Co Ltd Polyester composition

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4711916A (en) * 1982-09-30 1987-12-08 Nippon Steel Corporation Inorganic filler dispersed-resin composition
JPS63120756A (en) * 1986-11-10 1988-05-25 Kuraray Co Ltd Filled resin composition
JPH01210452A (en) * 1988-02-18 1989-08-24 Idemitsu Petrochem Co Ltd Glass fiber-reinforced polyester resin composition
WO1995029134A1 (en) * 1994-04-25 1995-11-02 Minnesota Mining And Manufacturing Company Compositions comprising fused particulates and methods of making them
US5641717A (en) * 1994-04-25 1997-06-24 Castle; Richard B. Compositions comprising fused particulates and methods of making same
US5883029A (en) * 1994-04-25 1999-03-16 Minnesota Mining And Manufacturing Company Compositions comprising fused particulates and methods of making them
US6045913A (en) * 1995-11-01 2000-04-04 Minnesota Mining And Manufacturing Company At least partly fused particulates and methods of making them by flame fusion
US6254981B1 (en) 1995-11-02 2001-07-03 Minnesota Mining & Manufacturing Company Fused glassy particulates obtained by flame fusion
CN109561791A (en) * 2016-08-04 2019-04-02 住友化学株式会社 Resin combination is used in flameproof ware, the manufacturing method of flameproof ware and flameproof ware forming
CN109561791B (en) * 2016-08-04 2022-03-04 住友化学株式会社 Ovenware, method for producing same, and resin composition for forming ovenware

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