JP3217092B2 - Reshaped product containing liquid crystal polymer - Google Patents

Reshaped product containing liquid crystal polymer

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Publication number
JP3217092B2
JP3217092B2 JP25238591A JP25238591A JP3217092B2 JP 3217092 B2 JP3217092 B2 JP 3217092B2 JP 25238591 A JP25238591 A JP 25238591A JP 25238591 A JP25238591 A JP 25238591A JP 3217092 B2 JP3217092 B2 JP 3217092B2
Authority
JP
Japan
Prior art keywords
liquid crystal
resin
melting point
liquid crystalline
crystalline polymer
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.)
Expired - Fee Related
Application number
JP25238591A
Other languages
Japanese (ja)
Other versions
JPH0586286A (en
Inventor
敬 富田
政克 大杉
祐之 松田
満晴 金子
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.)
Mazda Motor Corp
Original Assignee
Mazda Motor Corp
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 Mazda Motor Corp filed Critical Mazda Motor Corp
Priority to JP25238591A priority Critical patent/JP3217092B2/en
Priority to EP19920116771 priority patent/EP0535650A3/en
Priority to KR1019920017834A priority patent/KR960006785B1/en
Publication of JPH0586286A publication Critical patent/JPH0586286A/en
Application granted granted Critical
Publication of JP3217092B2 publication Critical patent/JP3217092B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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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、液晶性ポリマーを含有
する再成形品の製造方法に関する
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention contains a liquid crystalline polymer.
The present invention relates to a method for producing a reshaped product .

【0002】[0002]

【従来の技術】従来、高強度で高剛性を有する合成樹脂
製成形品としては、熱硬化性樹脂にガラス繊維を混合し
たものや、スタンパブルシートと称される熱可塑性樹脂
に長繊維ガラスを混合したものなどを所定形状に成形す
ることにより得られるものが知られている。また、上記
ガラス繊維の代わりに炭素繊維を用いてなる高強度且つ
高剛性の合成樹脂も知られている。
2. Description of the Related Art Conventionally, molded articles made of synthetic resin having high strength and high rigidity include those obtained by mixing glass fibers with a thermosetting resin, or those made of long fiber glass in a thermoplastic resin called a stampable sheet. What is obtained by shaping the mixture etc. into a predetermined shape is known. A high-strength and high-rigidity synthetic resin using carbon fiber instead of the glass fiber is also known.

【0003】さらに、ガラス繊維や炭素繊維が混合され
ない高強度で高剛性を有する合成樹脂成形品として、特
開平1−320128号公報に示されるように、熱可塑
性樹脂と液晶樹脂(液晶ポリマー)とからなる複合材を液
晶樹脂の液晶転移温度以上の温度下で延伸しながら押出
すことにより得たストランドを1〜40mmの長さに切断
し、得られた切断物を液晶樹脂の液晶転移温度以下の温
度で押出成形することにより得られるものも知られてい
る。
Further, as a synthetic resin molded article having high strength and high rigidity in which glass fibers and carbon fibers are not mixed, as disclosed in JP-A-1-320128, a thermoplastic resin and a liquid crystal resin (liquid crystal polymer) are used. Strand obtained by extruding while stretching the composite material comprising the liquid crystal resin at a temperature equal to or higher than the liquid crystal transition temperature is cut into a length of 1 to 40 mm, and the obtained cut product is equal to or lower than the liquid crystal transition temperature of the liquid crystal resin. Is also known by extrusion at a temperature of.

【0004】ところで、近時、資源保護等の観点から成
形品となった合成樹脂体をリサイクル(再成形)すること
が望まれている。合成樹脂体よりなる成形品をリサイク
ルする場合には、合成樹脂体を粉砕して合成樹脂よりな
る粉砕片を得た後、該粉砕片を加熱して溶融し、次に、
溶融状態の合成樹脂材を所定形状の成形品に成形する
か、又は溶融状態の合成樹脂を押出成形して成形用素材
を得た後、その成形用素材を所定形状の成形品に成形す
るものである。
Recently, it has been desired to recycle (re-mold) a synthetic resin body which has become a molded product from the viewpoint of resource protection and the like. When recycling a molded article made of a synthetic resin body, after crushing the synthetic resin body to obtain a crushed piece made of a synthetic resin, heating and melting the crushed piece,
Molding a synthetic resin material in a molten state into a molded product of a predetermined shape, or extruding a synthetic resin in a molten state to obtain a molding material, and then molding the molding material into a molded product of a predetermined shape It is.

【0005】従来、高強度で高剛性を有する合成樹脂体
をリサイクルする場合には、ガラス繊維や炭素繊維等の
強化用繊維を合成樹脂に混合してなる繊維強化樹脂体が
対象になっていた。
Conventionally, when recycling a synthetic resin body having high strength and high rigidity, a fiber reinforced resin body obtained by mixing reinforcing fibers such as glass fiber and carbon fiber with a synthetic resin has been targeted. .

【0006】[0006]

【発明が解決しようとする課題】しかるに、上記のよう
な繊維強化樹脂体を再成形する場合、繊維強化樹脂体を
粉砕して得られた粉砕片においては合成樹脂体に混入さ
れている強化用繊維が短く切断されているために、再成
形により得られた成形用素材においても強化用繊維が切
断されたままである。このため、リサイクルによる得ら
れた再成形品は、当初の成形品に比べて強度及び剛性の
点で低下せざるを得なかった。
However, when the above-mentioned fiber reinforced resin body is re-formed, the crushed pieces obtained by crushing the fiber reinforced resin body have a reinforcing material mixed in the synthetic resin body. Since the fibers are cut short, the reinforcing fibers remain cut even in the molding material obtained by reshaping. For this reason, the remolded product obtained by recycling had to be reduced in strength and rigidity as compared with the original molded product.

【0007】上記に鑑み、本発明は、高強度で高剛性を
有する合成樹脂体を再成形して得られる再成形品の強度
及び剛性を当初の合成樹脂体よりも低下しないようにす
ることを目的とする。
In view of the above, an object of the present invention is to prevent the strength and rigidity of a reshaped product obtained by reshaping a high-strength, high-rigidity synthetic resin body from lowering than the original synthetic resin body. Aim.

【0008】[0008]

【課題を解決するための手段】即ち本発明は、ナイロン
であるマトリックス樹脂および該マトリックス樹脂より
高い融点を有する液晶性ポリマー40〜80重量%を含
有して成形され、上記マトリックス樹脂中において、液
晶性ポリマーが繊維化されてなる複合成形品を粉砕し、
次いで粉砕材を上記液晶性ポリマーの融点よりも高温に
加熱溶融して再成形用材料を上記液晶性ポリマー分子に
配向性を付与する状態で調製した後、上記マトリックス
樹脂の融点以上で液晶性ポリマーの融点未満の温度で成
形することにより上記液晶性ポリマーの繊維状液晶化物
のアスペクト比3以上に設定するようにしたことを特徴
とする液晶性ポリマーを含有する再成形品の製造方法
を、提供する。
That is, the present invention relates to nylon.
And a matrix resin which is
Contains 40 to 80% by weight of a liquid crystalline polymer having a high melting point
In the matrix resin, the liquid
Molded product made of crystalline polymerCrush the
ThenMake the crushed material higher than the melting point of the above liquid crystalline polymer
Heat and melt to transform the remolding material into the above liquid crystalline polymer molecules
After preparing in a state to give orientation, the above matrix
At a temperature above the melting point of the resin but below the melting point of the liquid crystalline polymer.
By shapingFibrous liquid crystal of the above liquid crystalline polymer
The feature is to set the aspect ratio of 3 or more
For producing reshaped article containing liquid crystalline polymer to be used
I will provide a.

【0009】本発明の再成形品に於いて使用されるマト
リックス樹脂であるナイロンは、市販品として入手出来
る。具体的には市販品としては、例えば1013B[宇
部興産(株)製]、CM1017(東レ(株)製)、テクニ
ールC216(昭和電工(株)製)等が挙げられ、これらの
1種以上使用してよい。特にナイロン6が好ましい。マ
トリックス樹脂の含有量は、樹脂組成物全重量に対し2
0〜60重量%が好ましい。マトリックス樹脂が20重
量%未満だと樹脂組成物の成形性が低下し、又60重量
%を超過すると成形物の強度が十分でなくなる。
Nylon, which is a matrix resin used in the reshaped product of the present invention, is commercially available. Specifically, examples of commercially available products include 1013B (manufactured by Ube Industries, Ltd.), CM1017 (manufactured by Toray Industries, Inc.), Technil C216 (manufactured by Showa Denko KK), and the like. May do it. Particularly, nylon 6 is preferable. The content of the matrix resin is 2 to the total weight of the resin composition.
0-60% by weight is preferred. When the amount of the matrix resin is less than 20% by weight, the moldability of the resin composition is reduced.

【0010】本発明の再成形品は、液晶性ポリマーを含
有する。液晶性ポリマーは、成形物中に於いて、後述の
アスペクト比を有する繊維形状をなし、成形物の強化材
となる。このような液晶性ポリマーとしては、上記マト
リックス樹脂より融点が高いもの、好ましくは20℃以
上高いものである。融点がマトリックス樹脂より低い
と、液晶性ポリマーが成形物中に於いて繊維状とならず
又配向も一定せず十分な強度が得られない。液晶ポリマ
ーとしては従来公知の各種のものが適用出来、特に限定
されるものではない。液晶ポリマーとしては、各種のも
のが知られているが、本発明で特に好ましく用いられる
ものは熱可塑性の液晶ポリエステル、また液晶ポリエス
テルアミドである。かかるものとして、特に好ましく用
いられるものとしては、下記に記載するものが挙げられ
る。即ち
The reshaped product of the present invention contains a liquid crystalline polymer. The liquid crystalline polymer forms a fiber shape having an aspect ratio described later in the molded product, and serves as a reinforcing material for the molded product. Such a liquid crystalline polymer has a higher melting point than that of the matrix resin, and preferably has a higher melting point by 20 ° C. or more. If the melting point is lower than that of the matrix resin, the liquid crystalline polymer does not become fibrous in the molded product, the orientation is not constant, and sufficient strength cannot be obtained. As the liquid crystal polymer, various conventionally known ones can be applied, and there is no particular limitation. Various types of liquid crystal polymers are known, and particularly preferably used in the present invention are thermoplastic liquid crystal polyesters and liquid crystal polyester amides. Particularly preferred examples of such a material include those described below. That is

【0011】[0011]

【化1】 Embedded image

【0012】[0012]

【化2】 Embedded image

【0013】[0013]

【化3】 Embedded image

【0014】[0014]

【化4】 Embedded image

【0015】[0015]

【化5】 Embedded image

【0016】ここで、Σni=100である。そして、特
に好ましいのは各構造式のniが4以上である。
Here, Δni = 100. It is particularly preferable that ni of each structural formula is 4 or more.

【0017】また、各式において、ハロゲン等をはじ
め、各種の置換基が付加されていても良い。これらに示
されるものは本発明の変性ポリエステルと良好に溶融成
形しやすいので特に好ましい。また、高強度・高弾性率
の複合繊維としやすい。
In each formula, various substituents such as halogen may be added. These are particularly preferred because they are easily melt-molded with the modified polyester of the present invention. Moreover, it is easy to make a composite fiber having high strength and high elastic modulus.

【0018】同様に液晶ポリエステルアミドも従来公知
のものが適用できなんら制限されるものではない。特に
好ましいものとして下記の構造式に示されるものが挙げ
られる。即ち
Similarly, a conventionally known liquid crystal polyesteramide can be applied, and the liquid crystal polyesteramide is not limited at all. Particularly preferred are those represented by the following structural formulas. That is

【0019】[0019]

【化6】 Embedded image

【0020】[0020]

【化7】 Embedded image

【0021】[0021]

【化8】 Embedded image

【0022】ここで、各構造式においてΣni=100で
ある。そして、特に好ましいのは各構造式のniが15以
上である。また、各式ともハロゲン等をはじめ、各種の
置換基が付加されていてもよい。これらに示されるもの
はポリアーリレートからなる液晶ポリマーと同様に溶融
成形性があり、かつ高強度である。液晶性ポリマーの含
有量は、樹脂組成物全重量に対し40〜80重量%であ
る。含有量が40重量%未満だと成形物に十分な強度を
付与できず、又80重量%を超過すると樹脂組成物の成
形性が低下する。
Here, Δni = 100 in each structural formula. It is particularly preferable that ni of each structural formula is 15 or more. In addition, various substituents such as halogen may be added to each formula. These compounds have melt moldability and high strength similarly to the liquid crystal polymer composed of polyarylate. The content of the liquid crystalline polymer is 40 to 80% by weight based on the total weight of the resin composition. If the content is less than 40% by weight, sufficient strength cannot be imparted to the molded product, and if it exceeds 80% by weight, the moldability of the resin composition is reduced.

【0023】本発明の樹脂組成物にはその他添加剤とし
て、耐光剤、酸化防止剤、可塑剤等を加えてよい。
The resin composition of the present invention may contain other additives such as a light stabilizer, an antioxidant and a plasticizer.

【0024】本発明の樹脂組成物は一旦溶融状態、即ち
液晶性ポリマーの融点より高い温度に加熱し、ポリマー
分子に配向性を付与する状態で成形あるいは成形用材料
化する。ポリマー分子に配向性を付与する状態は押出成
形、射出成形等の方法により与えられるのが一般的であ
る。この方法で直接、成形して、高い配向性(分子方向
性)を有する成形物品を得てもよい。しかし、通常押出
成形した後、ペレット状の成形用材料にする。この成形
用材料を用いて、再度押出機や射出成形器等で溶融して
成形する。この再溶融する時の温度はマトリックス樹脂
の融点より高くかつ液晶ポリマーの融点より低い温度で
ある方が、液晶樹脂が繊維状態を保持しているので好ま
しい。成形用材料としては平板状のものを用いてもよ
い。この場合成形用材料板を重ねて型内成形してもよ
い。特に、配向方向を同一または異なる方向にすること
により、成形物品の特性を変えることができる。
The resin composition of the present invention is once heated to a molten state, that is, a temperature higher than the melting point of the liquid crystalline polymer, and is molded or formed into a molding material in a state of imparting orientation to polymer molecules. The state of imparting the orientation to the polymer molecule is generally given by a method such as extrusion molding, injection molding or the like. Molding may be performed directly by this method to obtain a molded article having high orientation (molecular orientation). However, usually, after extrusion molding, it is made into a pellet-like molding material. Using this molding material, it is again melted and molded by an extruder, an injection molding machine or the like. It is preferable that the re-melting temperature be higher than the melting point of the matrix resin and lower than the melting point of the liquid crystal polymer, since the liquid crystal resin maintains a fibrous state. A flat material may be used as the molding material. In this case, the molding material plates may be stacked and molded in the mold. In particular, by making the orientation directions the same or different, the characteristics of the molded article can be changed.

【0025】上記再成形物中に複合された繊維状液晶化
ポリマーは、アスペクト比(即ち、長さ/太さ)3以上、
好ましくは10以上有する。
The fibrous liquid crystalline polymer composited in the reshaped product has an aspect ratio (ie, length / thickness) of 3 or more,
Preferably, it has 10 or more.

【0026】[0026]

【発明の効果】上記成形物を原料として、これを必要に
応じ粉砕等を行い、上記製造法に従って再溶融、再成形
を行うことにより、再成形物が得られる。このようにし
て得られた再成形物中の繊維状液晶化ポリマーは本質的
に原料成形物中のそれと同じであり、アスペクト比3以
上を有し、従って再成形物は原料成形物の強度と実質的
に同等である。このような再成形物も更に、何度でも再
成形出来、実質的に強度低下のない再成形物を与える。
According to the present invention, a reshaped product is obtained by using the above-mentioned shaped material as a raw material, pulverizing the material as necessary, and re-melting and re-molding according to the above-mentioned production method. The fibrous liquid crystalline polymer in the remolded product thus obtained is essentially the same as that in the raw molded product, and has an aspect ratio of 3 or more. Substantially equivalent. Such reshaped articles can also be reshaped any number of times, giving reshaped articles with substantially no loss in strength.

【0027】[0027]

【実施例】以下、本発明を実施例により具体的に説明す
る。まず、液晶樹脂としてポリプラスチックス(株)製の
ベクトラA950(芳香族ポリエステル、液晶転移温度:
約280℃)を用い、ナイロン−6としては宇部興産
(株)製の1013Bを用い、両者を所定の割合に混合し
て液晶樹脂複合材を得た。
The present invention will be described below in more detail with reference to examples. First, as a liquid crystal resin, Vectra A950 manufactured by Polyplastics Co., Ltd. (aromatic polyester, liquid crystal transition temperature:
About 280 ° C) and Ube Industries as nylon-6
A liquid crystal resin composite material was obtained by mixing both at a predetermined ratio using 1013B manufactured by Co., Ltd.

【0028】次に、上記液晶樹脂複合材を初期押出成形
した。この場合の押出成形条件は、押出機としてプラス
チック工学研究所(株)製の2軸押出機(スクリュー径:3
0mm)を用い、樹脂温度は290℃に、スクリュー回転
数は100rpmに、ダイス径は2mmに、剪断速度は17
00sec-1に、延伸比は2倍に各々設定した。そして、
上記の液晶樹脂複合材を延伸しながら押出成形してテス
ト用の直径:1.4mmのストランド状の初期成形用素材
を得た後、該初期成形用素材の一部を長さ:3mmに切断
して初期ペレット材を得た。
Next, the above liquid crystal resin composite material was initially extruded. In this case, the extrusion conditions were as follows: a twin-screw extruder (screw diameter: 3) manufactured by Plastic Engineering Laboratory Co., Ltd. was used as the extruder.
0 mm), a resin temperature of 290 ° C., a screw rotation speed of 100 rpm, a die diameter of 2 mm, and a shear rate of 17 mm.
At 00 sec −1 , the stretching ratio was set to 2 times. And
The liquid crystal resin composite material was extruded while being stretched to obtain a strand-shaped initial molding material having a diameter of 1.4 mm for a test, and a part of the initial molding material was cut into a length of 3 mm. Thus, an initial pellet material was obtained.

【0029】次に、上記初期ペレット材を射出成形して
液晶樹脂複合体を得た。この場合の射出成形条件は、東
芝機械(株)製の220Ton射出成形機及びテストピース
型の金型を用い、樹脂温度を250℃に設定した。ま
た、この場合に、上記の射出成形機及びスパイラルフロ
ー型(直径:6mmの半円形)の金型を用い、樹脂温度を2
50℃に、射出圧を1000kg/cm2に各々設定して流
動性評価テストを行なった。
Next, the initial pellet material was injection molded to obtain a liquid crystal resin composite. The injection molding conditions in this case were such that a 220 Ton injection molding machine manufactured by Toshiba Machine Co., Ltd. and a test piece mold were used, and the resin temperature was set to 250 ° C. Further, in this case, the injection molding machine and the spiral flow type (semicircular with a diameter of 6 mm) mold were used, and the resin temperature was set at 2.
A fluidity evaluation test was performed at 50 ° C. and an injection pressure of 1000 kg / cm 2 .

【0030】次に、上記液晶樹脂複合体を、(株)ホーラ
イ製 V−360の粉砕装置で粉砕し、長さ:3〜4mm
の粉砕片を得た後、該粉砕片をリサイクル押出し成形し
てテスト用の直径:1.4mmのストランド状のリサイク
ル成形用素材を得た後、該リサイクル成形用素材の一部
を長さ:3mmに切断してリサイクルペレット材を得た。
この場合の押出成形条件は初期押出成形の場合と同じで
あった。
Next, the liquid crystal resin composite was pulverized with a pulverizer of V-360 manufactured by Horai Co., Ltd., and the length was 3 to 4 mm.
After obtaining the crushed pieces of the above, the crushed pieces are recycled and extruded to obtain a strand-shaped recycle molding material having a diameter of 1.4 mm for a test, and a part of the recycle molding material has a length of: It was cut into 3 mm to obtain a recycled pellet material.
The extrusion molding conditions in this case were the same as in the case of the initial extrusion molding.

【0031】次に、ストランド状の初期成形用素材及び
リサイクル成形用素材に対して引張試験を行なった。測
定機としては島津製作所(株)製の万能試験機(オートグ
ラフ)を用い、引張速度を20mm/分に設定した。
Next, a tensile test was performed on the strand-shaped initial molding material and the recycled molding material. A universal testing machine (Autograph) manufactured by Shimadzu Corporation was used as a measuring machine, and the tensile speed was set to 20 mm / min.

【0032】図1は初期成形用素材及びリサイクル成形
用素材に対して引張試験を行なった結果を示しており、
液晶樹脂の含有率が40%を超える領域で液晶樹脂の繊
維化が生じ、液晶樹脂含有量の全量域に亘って両者の引
張強度が略同じであること、つまり上記再成形方法によ
ると高強度の合成樹脂を再成形するにも拘わらず、強度
が低下しないことが確認できた。
FIG. 1 shows the results of a tensile test performed on the initial molding material and the recycled molding material.
In the region where the content of the liquid crystal resin exceeds 40%, the liquid crystal resin becomes fibrous, and the tensile strengths of the two are substantially the same over the entire range of the content of the liquid crystal resin. It was confirmed that the strength did not decrease in spite of the re-molding of the synthetic resin.

【0033】図2は液晶樹脂含有量と流動長比との関係
を示しており、液晶樹脂含有量が80%を超えると流動
性が極端に低下し、成形用材料としては用い難いことが
明らかになった。以上の考察から、熱可塑性樹脂として
ナイロン−6を用いる場合には、液晶樹脂の含有量が4
0〜80%の範囲内であることが好ましい。
FIG. 2 shows the relationship between the liquid crystal resin content and the flow length ratio. It is clear that when the liquid crystal resin content exceeds 80%, the fluidity is extremely reduced, and it is difficult to use as a molding material. Became. From the above considerations, when nylon-6 is used as the thermoplastic resin, the content of the liquid crystal resin is 4%.
It is preferable that it is in the range of 0 to 80%.

【0034】また、初期成形用素材及びリサイクル成形
用素材に対して電子顕微鏡(SEM)による形態観察を行
なったところ、液晶樹脂の含有量が40%のときには液
晶樹脂の大部分は粒状であり一部分が繊維状であった。
また、液晶樹脂の含有量が50%のときには液晶樹脂は
繊維状であった。この結果から、液晶樹脂が40%以上
含有されると、液晶樹脂が繊維化して引張強度が向上す
ることが理解できる。
When the morphological observation of the material for initial molding and the material for recycling molding was performed by an electron microscope (SEM), when the content of the liquid crystal resin was 40%, most of the liquid crystal resin was granular, and Was fibrous.
When the content of the liquid crystal resin was 50%, the liquid crystal resin was fibrous. From this result, it can be understood that when the content of the liquid crystal resin is 40% or more, the liquid crystal resin is fiberized and the tensile strength is improved.

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

【図1】 実施例により得られた初期成形用素材および
リサイクル成形用素材に対する引張試験の結果を示すグ
ラフである。
FIG. 1 is a graph showing the results of a tensile test on a material for initial molding and a material for recycling molding obtained in Examples.

【図2】 実施例により得られた成形物中の液晶樹脂含
有量と流動長比を示すグラフである。
FIG. 2 is a graph showing a liquid crystal resin content and a flow length ratio in a molded product obtained in an example.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 金子 満晴 広島県安芸郡府中町新地3番1号 マツ ダ株式会社内 (56)参考文献 特開 平3−24911(JP,A) 特開 平5−70700(JP,A) (58)調査した分野(Int.Cl.7,DB名) C08L 1/00 - 101/16 ────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Mitsuharu Kaneko 3-1 Shinchi, Fuchu-cho, Aki-gun, Hiroshima Mazda Co., Ltd. (56) References JP-A-3-24911 (JP, A) JP-A-5 -70700 (JP, A) (58) Field surveyed (Int. Cl. 7 , DB name) C08L 1/00-101/16

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ナイロンであるマトリックス樹脂および
該マトリックス樹脂より高い融点を有する液晶性ポリマ
ー40〜80重量%を含有して成形され、上記マトリッ
クス樹脂中において、液晶性ポリマーが繊維化されてな
る複合成形品を粉砕し、次いで粉砕材を上記液晶性ポリ
マーの融点よりも高温に加熱溶融して再成形用材料を上
記液晶性ポリマー分子に配向性を付与する状態で調製し
た後、上記マトリックス樹脂の融点以上で液晶性ポリマ
ーの融点未満の温度で成形することにより上記液晶性ポ
リマーの繊維状液晶化物のアスペクト比3以上に設定す
るようにしたことを特徴とする液晶性ポリマーを含有す
る再成形品の製造方法
1. A composite comprising a matrix resin which is nylon and a liquid crystal polymer having a melting point higher than that of the matrix resin, which is 40 to 80% by weight, wherein the liquid crystal polymer is formed into fibers in the matrix resin. After the molded article is pulverized and then the pulverized material is heated and melted to a temperature higher than the melting point of the liquid crystalline polymer to prepare a remolding material in a state of imparting orientation to the liquid crystalline polymer molecules, the liquid crystalline port by molding at a temperature below the liquid crystal polymer melting point above the melting point
Set the aspect ratio of the remeric fibrous liquid crystal to 3 or more.
Containing a liquid crystalline polymer characterized by
Manufacturing method for reshaped products .
【請求項2】 再成形品の液晶性ポリマー繊維状液晶化
物がアスペクト比10以上である請求項1記載の製造方
2. The method according to claim 1, wherein the liquid crystalline polymer fibrous liquid crystal of the reshaped product has an aspect ratio of 10 or more.
Law .
【請求項3】 液晶性ポリマーの融点がマトリックス樹
脂のそれより20℃以上高い請求項1記載の製造方法
3. The process for producing the melting point of the liquid crystalline polymer it than 20 ° C. or higher high claim 1, wherein the matrix resin.
JP25238591A 1991-09-30 1991-09-30 Reshaped product containing liquid crystal polymer Expired - Fee Related JP3217092B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP25238591A JP3217092B2 (en) 1991-09-30 1991-09-30 Reshaped product containing liquid crystal polymer
EP19920116771 EP0535650A3 (en) 1991-09-30 1992-09-30 Molding resin composition
KR1019920017834A KR960006785B1 (en) 1991-09-30 1992-09-30 Molding resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25238591A JP3217092B2 (en) 1991-09-30 1991-09-30 Reshaped product containing liquid crystal polymer

Publications (2)

Publication Number Publication Date
JPH0586286A JPH0586286A (en) 1993-04-06
JP3217092B2 true JP3217092B2 (en) 2001-10-09

Family

ID=17236589

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25238591A Expired - Fee Related JP3217092B2 (en) 1991-09-30 1991-09-30 Reshaped product containing liquid crystal polymer

Country Status (1)

Country Link
JP (1) JP3217092B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6121388A (en) * 1998-05-12 2000-09-19 Toray Industries, Inc. Polyamide resin composition

Also Published As

Publication number Publication date
JPH0586286A (en) 1993-04-06

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