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JPH0611936B2 - Method for producing composite material for thermoforming - Google Patents
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JPH0611936B2 - Method for producing composite material for thermoforming - Google Patents

Method for producing composite material for thermoforming

Info

Publication number
JPH0611936B2
JPH0611936B2 JP62231742A JP23174287A JPH0611936B2 JP H0611936 B2 JPH0611936 B2 JP H0611936B2 JP 62231742 A JP62231742 A JP 62231742A JP 23174287 A JP23174287 A JP 23174287A JP H0611936 B2 JPH0611936 B2 JP H0611936B2
Authority
JP
Japan
Prior art keywords
mat
composite material
thickness
resin component
thermoforming
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 - Lifetime
Application number
JP62231742A
Other languages
Japanese (ja)
Other versions
JPS6477663A (en
Inventor
昌博 塚本
正彦 石田
克彦 山路
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical 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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP62231742A priority Critical patent/JPH0611936B2/en
Priority to US07/233,282 priority patent/US4923547A/en
Priority to DE88307649T priority patent/DE3882628T2/en
Priority to EP88307649A priority patent/EP0308074B1/en
Priority to CA 575144 priority patent/CA1309822C/en
Priority to AU21199/88A priority patent/AU618550B2/en
Publication of JPS6477663A publication Critical patent/JPS6477663A/en
Priority to US07/485,631 priority patent/US5055341A/en
Publication of JPH0611936B2 publication Critical patent/JPH0611936B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Laminated Bodies (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Nonwoven Fabrics (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は熱成形性のすぐれた複合材料、特に自動車の天
井材として好適に使用される複合材料の製造方法に関す
る。
TECHNICAL FIELD The present invention relates to a method for producing a composite material having excellent thermoformability, particularly a composite material preferably used as a ceiling material for automobiles.

〔従来の技術〕[Conventional technology]

従来、自動車の内装材のひとつである成形天井材の基材
としては、ダンボール、ガラス繊維強化熱硬化性樹脂シ
ート等が使用されていたが、ダンボールは熱賦形性が悪
く、吸音性がなく、又吸湿性なので長期間使用している
と水分を吸って重くなりたれが生じるという欠点を有
し、上記熱硬化性樹脂シートはシートの生産性が低く熱
賦形性が悪くかつ重いという欠点を有していた。
Conventionally, cardboard, glass fiber reinforced thermosetting resin sheet, etc. have been used as the base material for molded ceiling material, which is one of the interior materials for automobiles.However, cardboard has poor heat shaping properties and no sound absorption. In addition, since it is hygroscopic, it has a drawback that it absorbs water and becomes heavy when used for a long period of time, and the thermosetting resin sheet has low productivity and poor heat shaping property and is heavy. Had.

これらの欠点を解消するために種々の提案がなされてお
り、たとえば実開昭58−15035号公報にはスチレ
ン系樹脂発泡シートの両面にガラス繊維強化熱可塑性樹
脂フイルムが積層されている積層体の一面に軟質合成樹
脂発泡体と塩化ビニルレザーが順次積層された自動車用
内装材が記載されている。
Various proposals have been made to solve these drawbacks. For example, Japanese Utility Model Laid-Open No. 58-15035 discloses a laminate in which a glass fiber reinforced thermoplastic resin film is laminated on both sides of a styrene resin foam sheet. An automobile interior material in which a soft synthetic resin foam and vinyl chloride leather are sequentially laminated on one surface is described.

上記内装材は、耐熱性、機械的強度がすぐれているが比
較的重く、吸音性がなく、コストが高いという欠点を有
していた。
The above-mentioned interior material has excellent heat resistance and mechanical strength, but it is relatively heavy, has no sound absorption, and has the drawbacks of high cost.

又、特開昭60−83832号公報にはガラス繊維層の
両面に熱可塑性樹脂層が積層された基材に樹脂層に発泡
体層及び表皮を積層した自動車天井材が記載されてい
る。
Further, JP-A-60-83832 discloses an automobile ceiling material in which a foam layer and a skin are laminated on a resin layer on a base material in which a thermoplastic resin layer is laminated on both sides of a glass fiber layer.

上記基材は薄肉で機械的強度が大きくかつ熱賦形性はす
ぐれているが、吸音性、断熱性等が不足しており、自動
車用天井材としては発泡体等を積層する必要があり、全
体としては熱賦形性が不足していた。
The base material is thin, has high mechanical strength and excellent heat formability, but lacks sound absorbing properties, heat insulating properties, etc., and it is necessary to laminate a foam or the like as an automobile ceiling material, As a whole, the heat formability was insufficient.

〔本発明が解決しようとする問題点〕[Problems to be Solved by the Present Invention]

本発明は上記欠点に鑑み、軽量で耐熱性、機械的強度、
吸音性等がすぐれ、熱賦形性がすぐれており生産性が高
く、コストが安く、特に自動車の天井材として好適に使
用できる熱成形用複合材料を製造する方法を提供するこ
とを目的とする。
In view of the above drawbacks, the present invention is lightweight and heat resistant, mechanical strength,
An object of the present invention is to provide a method for producing a thermoforming composite material which has excellent sound absorption properties, excellent heat shaping properties, high productivity, low cost, and particularly suitable for use as an automobile ceiling material. .

〔問題点を解決するための手段〕[Means for solving problems]

本発明で使用されるマット状物は無機繊維と、熱可塑性
樹脂繊維及び熱可塑性樹脂粉末からなる群から選ばれた
少なくとも一種の樹脂成分よりなるものである。
The mat-like material used in the present invention comprises inorganic fibers and at least one resin component selected from the group consisting of thermoplastic resin fibers and thermoplastic resin powders.

上記無機繊維としては、たとえばガラス繊維、ロックウ
ール等があげられ、その長さはマット状物の形成性の点
から5〜200mmが好ましく50mm以上のものが70重
量%以上含まれているのがより好ましい。又、その太さ
は細くなると機械的強度が低下し、太くなると重くなっ
て嵩密度が小さくなるので5〜30μmが好ましく、よ
り好ましくは7〜20μmである。
Examples of the inorganic fibers include glass fibers and rock wool, and the length thereof is preferably 5 to 200 mm from the viewpoint of forming a mat-like material, and 70% by weight or more of 50 mm or more is contained. More preferable. Further, the thickness is preferably 5 to 30 μm, more preferably 7 to 20 μm because the mechanical strength decreases as the thickness decreases, and the bulk density decreases as the thickness increases.

又、上記熱可塑性樹脂繊維及び熱可塑性樹脂粉末として
は、たとえば、ポリエチレン、ポリプロピレン、飽和ポ
リエステル、ポリアミド、ポリスチレン、ポリビニルブ
チラール、ポリウレタン等の熱可塑性樹脂よりなる繊維
及び粉末があげられる。熱可塑性樹脂繊維の長さ及び直
径は無機繊維と混繊してマット状物を形成する際の形成
性がすぐれているのが好ましいので、長さは5〜200
mmが好ましく、より好ましくは20〜100mmであり、
太さは3〜50μmが好ましく、より好ましくは20〜
40μmである。又熱可塑性樹脂粉末の直径は粉末状態
で添加される際には50〜100メッシュが好ましく、
貧溶媒に分散された状態もしくはエマルジョンにして添
加される際にはもっと小さくてよい。
Examples of the thermoplastic resin fibers and thermoplastic resin powders include fibers and powders made of thermoplastic resins such as polyethylene, polypropylene, saturated polyester, polyamide, polystyrene, polyvinyl butyral and polyurethane. The length and the diameter of the thermoplastic resin fiber are preferably 5 to 200 because the formability when forming a mat-like material by mixing with the inorganic fiber is excellent.
mm is preferred, more preferably 20-100 mm,
The thickness is preferably 3 to 50 μm, more preferably 20 to
It is 40 μm. The diameter of the thermoplastic resin powder is preferably 50 to 100 mesh when added in powder form,
It may be smaller when it is dispersed in a poor solvent or added as an emulsion.

無機繊維と樹脂成分の添加量は、無機繊維の比率が大き
くなると樹脂成分の比率が小さくなって無機繊維同志の
接着点が少なくなり、又逆に無機繊維の比率が小さくな
ると樹脂成分の比率が多くなるので共に機械的強度徳い
剛性が低下するので、1:5〜10:1(重量比)の範
囲が好ましい。
The amount of the inorganic fiber and the resin component added is such that when the ratio of the inorganic fiber is large, the ratio of the resin component is small and the adhesive points between the inorganic fibers are small, and conversely when the ratio of the inorganic fiber is small, the ratio of the resin component is small. Since it increases, the mechanical strength and rigidity decrease together, so that the range of 1: 5 to 10: 1 (weight ratio) is preferable.

マット状物の密度は大きくなると重くなり、小さくなる
と機械的強度が低下するので0.01〜0.2g/cm3
が好ましく、より好ましくは0.03〜0.07g/cm3
ある。
If the density of the mat-like material increases, it becomes heavier, and if it decreases, the mechanical strength decreases, so 0.01-0.2 g / cm 3
Is preferable, and more preferably 0.03 to 0.07 g / cm 3 .

上記マット状物の製造方法は任意の方法が採用されてよ
く、たとえば無機繊維と樹脂成分をカードマシンに供給
し、解繊、混繊しマット状物を製造する方法があげられ
る。
Any method may be adopted as the method for producing the mat-like material, and examples thereof include a method of supplying inorganic fibers and a resin component to a card machine to defibrate and mix them to produce a mat-like material.

尚、熱可塑性樹脂粉末はマット状物の製造後添加されて
もよいし、貧溶媒に分散された状態もしくはエマルジョ
ンにしてマット状物に散布したり、マット状物を浸漬し
てもよい。
The thermoplastic resin powder may be added after the production of the mat-like material, or may be dispersed in a poor solvent or made into an emulsion and sprayed on the mat-like material, or the mat-like material may be dipped.

又、マット状物の機械的強度を向上させるためにニード
ルパンチを施こしてもよく、ニードルパンチは1cm2
り1〜3個所行なわれるのが好ましい。
Needle punching may be carried out in order to improve the mechanical strength of the mat-like material. Needle punching is preferably carried out at 1 to 3 places per cm 2 .

本発明で使用される板状体は上記樹脂成分が溶融状態で
は融着するが非融着状態では接着しない性質を有するも
のであり、たとえばガラス繊維強化ポリテトラフルオロ
エチレンシート、表面がポリテトラフルオロエチレン加
工されたプレス板、表面が離型処理されたポリエステル
シート等があげられる。
The plate-like body used in the present invention has a property that the above resin component is fused in a molten state but does not adhere in a non-fused state. For example, a glass fiber reinforced polytetrafluoroethylene sheet, the surface of which is polytetrafluoro Examples thereof include a press plate processed with ethylene and a polyester sheet whose surface is treated to be released.

本発明においては前記マット状の両面に上記板状体を積
層し、樹脂成分の溶融温度以上の温度に加熱して樹脂成
分を溶融せしめた状態で加圧圧縮する。
In the present invention, the plate-like bodies are laminated on both surfaces of the mat-like material, and the resin component is melted by heating it to a temperature equal to or higher than the melting temperature of the resin component and compressed under pressure.

上記加熱する方法は任意の方法が採用されてよく、たと
えば熱風加熱方法、赤外線ヒーター、遠赤外線ヒーター
などによる幅射加熱方法等があげられる。
As the heating method, any method may be adopted, and examples thereof include a hot air heating method, a radiant heating method using an infrared heater, a far infrared heater and the like.

尚、加熱と板状体の積層の順序はどちらでもよく、加熱
後積層してもよいし、積層後加熱してもよい。
The heating and the laminating of the plate-shaped bodies may be performed in either order, and may be laminated after heating or may be heated after laminating.

又、加圧圧縮も任意の方法が採用されてよく、たとえば
プレスする方法、ロールで圧縮する方法等があげられ
る。プレス圧力は0.1〜20kg/cm2が好ましく、圧
縮時間は数秒あればよい。又ロールで圧縮する際にはロ
ール間をマット状物の4/5〜1/20に設定するのが好
ましい。プレス、ロール共に圧縮する際には樹脂成分の
溶融温度以上の温度に加熱されているのが好ましい。本
発明においては加圧圧縮された、板状体が積層されたマ
ット状物は解圧され、樹脂成分が溶融した状態で板状体
が拡開されマット状物は厚みが増大されてから冷却され
る。
Further, any method may be adopted as the compression under pressure, and examples thereof include a pressing method and a rolling method. The pressing pressure is preferably 0.1 to 20 kg / cm 2 , and the compression time may be several seconds. When compressing with a roll, it is preferable to set the space between the rolls to 4/5 to 1/20. When both the press and the roll are compressed, it is preferable that they are heated to a temperature equal to or higher than the melting temperature of the resin component. In the present invention, the mat-like material in which the plate-like materials are compressed and compressed is decompressed, the plate-like material is expanded with the resin component melted, and the mat-like material is cooled after the thickness is increased. To be done.

加圧圧縮されると溶融した樹脂成分は無機繊維中に含浸
される。次に解圧するとマット状物は元の厚さに回復し
ようとするが無機繊維は一度押しつぶされているので充
分に回復しない。そこで樹脂成分が溶融した状態で板状
体を拡開してやるとマット状物は板状体に融着している
から厚みが回復され嵩高くなる。尚、この際樹脂成分は
溶融しているので無機繊維や接着部分が破断することは
ない。又、拡開の方法は、たとえば板状体の両端を持っ
て行ってもよいし、真空吸引によって反対方向に引張し
てもよい。
The molten resin component is impregnated in the inorganic fiber when compressed under pressure. Next, when the pressure is released, the mat-like material tries to recover to the original thickness, but the inorganic fiber is once crushed and thus does not recover sufficiently. Therefore, if the plate-shaped body is expanded with the resin component melted, the mat-shaped material is fused to the plate-shaped body, so that the thickness is recovered and the volume becomes bulky. At this time, since the resin component is melted, the inorganic fibers and the bonded portion are not broken. Further, the expanding method may be carried out, for example, by holding both ends of the plate-shaped body, or may be pulled in the opposite direction by vacuum suction.

拡開されて嵩高くなったマット状物は次に冷却される
が、冷却は放冷であってもよいし冷風を吹き付けてもよ
い。冷却して樹脂成分が固化した後に板状体を剥離する
と熱成形用複合材料が得られる。
The mat-like material that has been expanded and made bulky is then cooled, but the cooling may be allowed to cool or blow cold air. When the plate-shaped body is peeled off after the resin component is solidified by cooling, a thermoforming composite material is obtained.

上記マット状物には加熱前に熱可塑性樹脂フイルムを積
層してもよい。
A thermoplastic resin film may be laminated on the mat-like material before heating.

上記熱可塑性樹脂フイルムとしては、ポリエチレン、ポ
リプロピレン、ポリスチレン、飽和ポリエステル等の熱
可塑性樹脂のフイルムがあげられる。
Examples of the thermoplastic resin film include thermoplastic resin films such as polyethylene, polypropylene, polystyrene, and saturated polyester.

熱可塑性樹脂フイルムの厚さは厚くなると重くなり、薄
くなると機械的強度が低下するので50〜500μmが
好ましく、より好ましくは70〜300μmである。
The thickness of the thermoplastic resin film becomes heavier as it becomes thicker, and the mechanical strength becomes lower as it becomes thinner, so that it is preferably 50 to 500 μm, more preferably 70 to 300 μm.

本発明の製造方法で得られた熱成形溶材料を賦形するに
は樹脂成分の溶融温度以上の温度に再加熱し、プレス等
で圧縮成形すればよく、自動車用天井材として使用する
には圧縮成形の際に塩化ビニルレザー、不織布等の化粧
用表皮材を積層して賦形すればよい。
In order to shape the thermoforming molten material obtained by the production method of the present invention, reheating to a temperature above the melting temperature of the resin component, compression molding with a press or the like may be performed, and it can be used as a ceiling material for automobiles. At the time of compression molding, a cosmetic skin material such as vinyl chloride leather or a non-woven fabric may be laminated and shaped.

〔実施例〕〔Example〕

次に本発明の実施例を説明する。 Next, examples of the present invention will be described.

実施例1 長さ40〜200mm、直径9〜13μmのガラス繊維と
長さ51mm、直径30μmのポリエチレン繊維(溶融温
度135℃)を2:1(重量比)の割合でカードマシン
に供給し混繊してマット状にし、1cm2当り2箇所ニー
ドルパンチを行って厚さ10mm重さ800g/m2のマッ
ト状物を得た。得られたマット状物の両面にガラス繊維
強化ポリテトラフルオロエチレンシート(厚さ150μ
m)を積層し、200℃で3分間加熱し、クリアランス
が1.3mmで、200℃に加熱したロールで圧縮し、2
00℃に保ってガラス繊維強化ポリテトラフルオロエチ
レンシートを両側から0.5mm/秒の速度で真空吸引、
マット状物の厚みを9mmまで回復し、その後3分間空冷
し、次いでシートを剥離して熱成形用複合材料を得た。
Example 1 Glass fibers having a length of 40 to 200 mm and a diameter of 9 to 13 μm and polyethylene fibers having a length of 51 mm and a diameter of 30 μm (melting temperature 135 ° C.) were supplied to a card machine at a ratio of 2: 1 (weight ratio) to mix fibers. A mat-like product having a thickness of 10 mm and a weight of 800 g / m 2 was obtained by needle punching at 2 points per cm 2 . Glass fiber reinforced polytetrafluoroethylene sheet (thickness 150μ
m) is laminated and heated at 200 ° C. for 3 minutes, and the clearance is 1.3 mm.
Vacuum suction of glass fiber reinforced polytetrafluoroethylene sheet from both sides at a rate of 0.5 mm / sec, keeping at 00 ° C.
The thickness of the mat-like material was recovered to 9 mm, followed by air cooling for 3 minutes, and then the sheet was peeled off to obtain a thermoforming composite material.

得られた複合材料を200℃のオーブンで2分間加熱し
た後30℃の金型で1kg/cm2の圧縮力で1分間圧縮し
成形体を得た。金型は最小肉厚部が3.0mm、最大肉厚
部が8.0mm、凹部の曲率半径が5mmであり、得られた
成形体は縦1400mm、横1150mmであった。
The obtained composite material was heated in an oven at 200 ° C. for 2 minutes and then compressed in a mold at 30 ° C. for 1 minute with a compression force of 1 kg / cm 2 to obtain a molded body. The mold had a minimum wall thickness of 3.0 mm, a maximum wall thickness of 8.0 mm, and a concave portion with a radius of curvature of 5 mm. The obtained molded product had a length of 1400 mm and a width of 1150 mm.

得られた成形体を95℃に設定された熱風乾燥機に供給
し、四辺を保持して24時間後の耐熱変位量(垂れ下っ
た距離)を測定した。又、厚さ6mm、幅50mm、長さ1
50mmの長方形の試料片を作成し、100mmの間隔をも
って配設された一対の支持体上に載置し、中央部を50
mm/分の速度で押圧して試料片が屈曲するときの荷重を
測定し曲げ強度を求めた。さらに垂直入射法により15
00Hzにおける吸音率を測定した。
The obtained molded body was supplied to a hot air dryer set at 95 ° C., the four sides were held, and the heat resistant displacement amount (hanging distance) after 24 hours was measured. Also, thickness 6mm, width 50mm, length 1
A rectangular sample piece of 50 mm is prepared and placed on a pair of supports arranged at intervals of 100 mm.
The bending strength was obtained by measuring the load when the sample piece was bent by pressing at a speed of mm / min. Furthermore, by the vertical incidence method, 15
The sound absorption coefficient at 00 Hz was measured.

又、熱成形性(金型の曲率半径5mmの凹部に対応する成
形体の部分の曲率半径)を測定して第1表に示した。
Further, the thermoformability (curvature radius of the portion of the molded body corresponding to the concave portion of the mold having a radius of curvature of 5 mm) was measured and shown in Table 1.

実施例2 実施例1で行ったと同様にしてガラス繊維とポリエチレ
ン繊維と混繊してマット状にし、1cm2当り1個所ニー
ドルパンチを行って厚さ10mm、重さ500g/m2にマ
ット状物を得、得られたマット状物の両面に厚さ150
μmのポリエチレンフイルム(溶融温度135℃)を積
層して積層シートを得た。得られた積層シートを用いて
実施例1で行ったと同様にして厚さ9.0mmの熱成形用
複合材料を得、成形体を得た。
Example 2 In the same manner as in Example 1, glass fibers and polyethylene fibers were mixed and formed into a mat-like material, and needle-punched at 1 point per 1 cm 2 to obtain a mat-like material having a thickness of 10 mm and a weight of 500 g / m 2 . And a thickness of 150 on both sides of the obtained mat-like material.
A polyethylene sheet (melting temperature: 135 ° C.) having a thickness of μm was laminated to obtain a laminated sheet. Using the obtained laminated sheet, a 9.0 mm-thick composite material for thermoforming was obtained in the same manner as in Example 1 to obtain a molded body.

得られた成形体の物性を実施例1で行ったと同様にして
測定し結果を第1表に示した。
The physical properties of the obtained molded product were measured in the same manner as in Example 1 and the results are shown in Table 1.

実施例3 実施例2で得られたマット状物を用いて実施例1で行っ
たと同様にして厚さ9mmの熱成形性複合材料を得、得ら
れた複合材料の両面に厚さ150μmのポリエチレンフ
イルムを積層した後実施例1で行ったと同様にして成形
体を得、物性を測定して結果を第1表に示した。
Example 3 Using the mat-like material obtained in Example 2, a thermoformable composite material having a thickness of 9 mm was obtained in the same manner as in Example 1, and a polyethylene having a thickness of 150 μm was formed on both sides of the obtained composite material. After laminating the films, a molded product was obtained in the same manner as in Example 1 and the physical properties were measured. The results are shown in Table 1.

比較例 実施例1で行ったと同様にしてロール圧縮した後放置し
て空冷し厚さ4.3mmの熱成形用複合材料を得た。得ら
れた複合材料を用い実施例1で行ったと同様にして成形
体を得、物性を測定して結果を第1表に示した。尚、曲
げ強度は厚さ4.3mmの試料で測定した。
Comparative Example Roll compression was performed in the same manner as in Example 1 and then the mixture was allowed to stand for air cooling to obtain a composite material for thermoforming having a thickness of 4.3 mm. A molded body was obtained using the obtained composite material in the same manner as in Example 1 and the physical properties were measured. The results are shown in Table 1. The bending strength was measured with a sample having a thickness of 4.3 mm.

〔発明の効果〕 本発明の熱成形用複合材料の製造方法は上述の通りであ
り、嵩高く軽量で熱賦形性がすぐれており、かつ耐熱
性、機械的強度、吸音性等がすぐれたコストの安い熱成
形用複合材料が容易に製造できる。
[Effects of the Invention] The method for producing the thermoforming composite material of the present invention is as described above, and it is bulky, lightweight, and has excellent heat shapeability, and also has excellent heat resistance, mechanical strength, sound absorption, and the like. A low-cost composite material for thermoforming can be easily manufactured.

又、得られた熱成形用複合材料は熱可塑性樹脂繊維もし
くは粉末が溶融されガラス繊維を有効に接着しているの
で熱成形性が良く、自動車の成形天井等に好適に使用さ
れる。
The obtained composite material for thermoforming has good thermoformability because the thermoplastic resin fiber or powder is melted and the glass fiber is effectively adhered to the composite material, and it is suitable for use in automobile molding ceilings and the like.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 // D06M 23/16 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location // D06M 23/16

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】無機繊維と、熱可塑性樹脂繊維及び熱可塑
性樹脂粉末からなる選ばれた少なくとも一種の樹脂成分
よりなるマット状物の両面に、上記樹脂成分が溶融状態
では融着するが非溶融状態では接着しない板状体を積層
し、上記樹脂成分の溶融温度以上の温度に加熱して樹脂
成分を溶融せしめた状態で加圧圧縮した後解圧し、上記
樹脂成分が溶融した状態で上記板状体を拡開し、マット
状物の厚みを増大させ次いで冷却することを特徴とする
熱成形複合材料の製造方法。
1. A mat-like material comprising inorganic fibers and at least one resin component selected from a thermoplastic resin fiber and a thermoplastic resin powder. In the state, laminated plate-like bodies which are not adhered to each other, are heated to a temperature not lower than the melting temperature of the resin component to cause the resin component to be melted under pressure and compression, and then decompressed. A method for producing a thermoformed composite material, which comprises expanding a sheet, increasing the thickness of a mat-like article, and then cooling.
JP62231742A 1987-08-20 1987-09-16 Method for producing composite material for thermoforming Expired - Lifetime JPH0611936B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP62231742A JPH0611936B2 (en) 1987-09-16 1987-09-16 Method for producing composite material for thermoforming
US07/233,282 US4923547A (en) 1987-08-20 1988-08-17 Process for producing composite molded articles from nonwoven mat
DE88307649T DE3882628T2 (en) 1987-08-20 1988-08-18 Composite molded parts and method for producing the same.
EP88307649A EP0308074B1 (en) 1987-08-20 1988-08-18 Composite molded articles and process for producing the same
CA 575144 CA1309822C (en) 1987-08-20 1988-08-18 Composite molded articles and process for producing same
AU21199/88A AU618550B2 (en) 1987-08-20 1988-08-22 Composite molded articles and process for producing same
US07/485,631 US5055341A (en) 1987-08-20 1990-02-27 Composite molded articles and process for producing same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62231742A JPH0611936B2 (en) 1987-09-16 1987-09-16 Method for producing composite material for thermoforming

Publications (2)

Publication Number Publication Date
JPS6477663A JPS6477663A (en) 1989-03-23
JPH0611936B2 true JPH0611936B2 (en) 1994-02-16

Family

ID=16928329

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62231742A Expired - Lifetime JPH0611936B2 (en) 1987-08-20 1987-09-16 Method for producing composite material for thermoforming

Country Status (1)

Country Link
JP (1) JPH0611936B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0773899B2 (en) * 1990-06-25 1995-08-09 積水化学工業株式会社 Method for manufacturing porous composite material
JPH06226740A (en) * 1993-02-03 1994-08-16 Sekisui Chem Co Ltd Production of fiber composite

Also Published As

Publication number Publication date
JPS6477663A (en) 1989-03-23

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