JPH04216030A - Manufacture of base material of interior material - Google Patents
Manufacture of base material of interior materialInfo
- Publication number
- JPH04216030A JPH04216030A JP2410841A JP41084190A JPH04216030A JP H04216030 A JPH04216030 A JP H04216030A JP 2410841 A JP2410841 A JP 2410841A JP 41084190 A JP41084190 A JP 41084190A JP H04216030 A JPH04216030 A JP H04216030A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- laminated
- film
- urethane
- glass fiber
- 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.)
- Withdrawn
Links
- 239000000463 material Substances 0.000 title claims description 38
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229920005989 resin Polymers 0.000 claims abstract description 19
- 239000011347 resin Substances 0.000 claims abstract description 19
- 239000003365 glass fiber Substances 0.000 claims abstract description 16
- 238000000465 moulding Methods 0.000 claims abstract description 10
- 229920006337 unsaturated polyester resin Polymers 0.000 claims abstract description 10
- 239000004745 nonwoven fabric Substances 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 8
- 238000010030 laminating Methods 0.000 claims description 2
- 239000002344 surface layer Substances 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract description 8
- -1 polypropylene Polymers 0.000 abstract description 8
- 239000004743 Polypropylene Substances 0.000 abstract description 7
- 229920001155 polypropylene Polymers 0.000 abstract description 7
- 239000011162 core material Substances 0.000 abstract description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract description 3
- 229920001577 copolymer Polymers 0.000 abstract description 3
- 239000004744 fabric Substances 0.000 abstract description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 238000000034 method Methods 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 5
- 229920000298 Cellophane Polymers 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 230000003014 reinforcing effect Effects 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920006327 polystyrene foam Polymers 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000012792 core layer Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 229920006248 expandable polystyrene Polymers 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000021189 garnishes Nutrition 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Moulding By Coating Moulds (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は内装材、特に成形天井、
ドアトリム、トランクトリム、ピラーガーニッシュ等の
自動車用或いはその他の車両や家具等の内装材の基材の
製造方法に関する。[Industrial Application Field] The present invention relates to interior materials, especially molded ceilings,
The present invention relates to a method for producing base materials for automobiles such as door trims, trunk trims, pillar garnishes, and interior materials for other vehicles and furniture.
【0002】0002
【従来の技術】従来より、主に成形天井に用いる内装材
基材としては例えば次のようなものがある。BACKGROUND OF THE INVENTION Heretofore, examples of interior material base materials mainly used for molded ceilings include the following.
【0003】
■レジンフェルト再生綿にフェノール樹脂を含浸させた
原反を、熱プレス成形型で圧縮成形し、樹脂を硬化させ
て一定形状のついた成形天井を製造する。
■ポリスチレン発泡シートポリスチレンの発泡体を非発
泡のポリスチレンシートでサンドイッチしたものを予備
加熱により柔らかくした状態で、その後直ちにプレス型
で成形する。
■段ボール紙を材料とする段ボールを熱プレス成形型で
圧縮成形し、一定形状のついた成形天井を製造する。[0003]Resin Felt An original fabric made of recycled cotton impregnated with phenolic resin is compression molded using a hot press mold, and the resin is cured to produce a molded ceiling with a certain shape. ■Polystyrene foam sheet A polystyrene foam sandwiched between non-foamed polystyrene sheets is softened by preheating and then immediately molded using a press mold. ■Cardboard made of corrugated paper is compressed and molded using a hot press mold to produce molded ceilings with a certain shape.
【0004】しかしながら、■の方法では成形する前の
状態では、樹脂と繊維材料とが結合していないため粉塵
が多く作業性が悪い。また必要十分な強度を得るために
は重量が大きくなる。更に高温や多湿の条件下で垂れ下
がりやすいという欠点がある。However, in the method (2), before molding, the resin and the fiber material are not bonded, so there is a lot of dust and the workability is poor. Moreover, in order to obtain the necessary and sufficient strength, the weight becomes large. Another drawback is that it tends to sag under high temperature and high humidity conditions.
【0005】又、■の方法では高温条件下で寸法変化が
大きく、寸法変化を吸収できる取り付け構造にする必要
があり、デザインに大きな制約が生じる。Furthermore, in method (2), dimensional changes are large under high-temperature conditions, and a mounting structure that can absorb the dimensional changes must be provided, which poses significant design constraints.
【0006】更に■の方法では紙に伸びがないため複雑
な形状には対応しきれず破れが生じるため、デザインの
自由度が低い。また表面に段ボールの凹凸が出てくるた
め表皮材にも制限がある。Furthermore, in method (2), since the paper does not stretch, it cannot accommodate complicated shapes and tears occur, so the degree of freedom in design is low. Furthermore, there are limitations to the surface material because the corrugated board has unevenness on its surface.
【0007】[0007]
【発明が解決しようとする課題】本発明の目的は軽量で
強度及びデザインの自由度が大きく且つ寸法変化の小さ
い内装材基材を良好な作業性により提供することにある
。SUMMARY OF THE INVENTION An object of the present invention is to provide an interior material base material that is lightweight, has great strength and freedom of design, and exhibits small dimensional changes with good workability.
【0008】[0008]
【課題を解決するための手段】本発明は集束したガラス
長繊維を一定長さに切断してランダム方向に均一に分散
したものにウレタン変性不飽和ポリエステル樹脂を含浸
させた後樹脂を穏やかな条件で増粘させて表面の粘着性
がなくなるまで熟成したものを、熱成形可能な繊維から
作られる嵩高い不織布の両面に積層し、熱プレス成形す
ることにより硬化・一体化することを特徴とする内装材
基材の製造方法に係る。[Means for Solving the Problems] The present invention involves cutting bundled long glass fibers to a certain length and uniformly dispersing them in random directions, impregnating them with a urethane-modified unsaturated polyester resin, and then applying the resin under mild conditions. The product is thickened and aged until the surface loses its tackiness, then it is laminated on both sides of a bulky nonwoven fabric made from thermoformable fibers, and is cured and integrated by hot press molding. It relates to a method for manufacturing interior material base materials.
【0009】本発明の内装材基材は図1に示すように熱
成形可能な繊維から作られる嵩高い不織布(1)の芯材
層(4)、及びガラス繊維(2)で補強されたウレタン
変性不飽和ポリエステル樹脂(3)の補強用面材(5)
からなる。As shown in FIG. 1, the interior material base material of the present invention includes a core material layer (4) of a bulky nonwoven fabric (1) made of thermoformable fibers, and a urethane layer reinforced with glass fibers (2). Reinforcing surface material (5) of modified unsaturated polyester resin (3)
Consisting of
【0010】本発明で使用される嵩高い不織布としては
、熱成形することができ、形状保持性を有する繊維から
作られた不織布を使用する。具体例としては、例えばカ
ネカロン(登録商標、アクリロニトリルと塩化ビニルの
共重合体)のようなポリアクリロニトリル系合成繊維単
独または該繊維とポリエステル等の混織からなる不織布
を挙げることができる。不織布の製造方法としては、■
ニードルパンチングに代表される機械的結合方法、■シ
ート状繊維に直接接着剤をスプレーまたは含浸させる化
学的結合方法、
■繊維長の長い単繊維集合体を開繊後、展綿積層した層
状体に熱可塑性または熱硬化性合成樹脂バインダーを含
浸、乾燥させる方法がある。カネカロンは加熱により硬
化する性質をもち、その特性とバインダー成分中に熱硬
化性樹脂(メラミン、エポキシ、フェノール樹脂等)を
添加することを組み合わせると成形後の芯材の剛性が高
くなるため好ましい。尚目付け量は、100〜1000
g/m2、好ましくは200〜600g/m2のものを
使用する。ガラス繊維は単繊維を集束剤で数十本から数
百本集束したストランドをそのままかもしくは何本か引
き揃えたもの(ロービング)を一定長さ(25〜60m
m)に切断しながらランダム方向に分散積層(50〜1
50g/m2、好ましくは100g/m2以下)させた
ものに、ウレタン変性不飽和ポリエステル樹脂を総量5
0〜300g/m2、好ましくは70〜200g/m2
程度含浸させて使用する。The bulky nonwoven fabric used in the present invention is a nonwoven fabric made from fibers that can be thermoformed and has shape retention properties. Specific examples include nonwoven fabrics made of polyacrylonitrile synthetic fibers such as Kanekalon (registered trademark, a copolymer of acrylonitrile and vinyl chloride) alone or in combination with such fibers and polyester. As for the manufacturing method of non-woven fabric, ■
Mechanical bonding methods represented by needle punching; ■Chemical bonding methods in which sheet fibers are directly sprayed or impregnated with adhesive. ■After opening a long single fiber aggregate, it is made into a layered product made by laminating spread cotton. There is a method of impregnating and drying a thermoplastic or thermosetting synthetic resin binder. Kanekalon has the property of being hardened by heating, and combining this property with the addition of a thermosetting resin (melamine, epoxy, phenol resin, etc.) to the binder component increases the rigidity of the core material after molding, which is preferable. The basis weight is 100 to 1000
g/m2, preferably 200 to 600 g/m2. Glass fibers are made by bundling tens to hundreds of single fibers with a sizing agent, either as is or by aligning several strands (roving) to a certain length (25 to 60 m).
Distributed lamination (50 to 1 m) in a random direction while cutting
50 g/m2, preferably 100 g/m2 or less), and a total amount of 50 g/m2 of urethane-modified unsaturated polyester resin.
0-300g/m2, preferably 70-200g/m2
Use after soaking to some extent.
【0011】本発明に使用するウレタン変性不飽和ポリ
エステル樹脂は不飽和基を有するポリエステルポリオー
ルとウレタン触媒及び不飽和基の架橋剤(通常スチレン
モノマー)とを混合したポリオール成分(これにポリエ
ーテルポリオール等を加える場合もある)と、イソシア
ネートと過酸化物とを混合したイソシアネート成分とを
混合することにより得られる。反応はまずポリオールと
イソシアネートとがウレタン触媒の影響でウレタン結合
し鎖長延長する。その後過酸化物触媒の影響で加熱下、
分子中の不飽和基とスチレンモノマー等の架橋剤とがラ
ジカル重合して高度に架橋した硬化樹脂となる。原料は
いずれも低分子量のものを用いている為、初期の粘度が
低く扱い易い。液状の樹脂は高温にならない限りウレタ
ン反応のみ進み不飽和結合の架橋反応は起こらない。ウ
レタン反応は触媒で調整できる為増粘を長時間遅らせる
こともできる。ウレタン反応が進み徐々に増粘して粘着
性を失う状態になつてもスチレンモノマーで希釈されて
いる為軟かい状態を保つており、これを加熱すると一旦
溶融した後硬化する性質を持ち長時間経過した後でも熱
成形することができる。硬化後の樹脂は通常の不飽和ポ
リエステルよりも耐衝撃性や強度といつた物性が向上し
、成形時の収縮も小さく、ポリウレタンにない耐熱性を
有する。The urethane-modified unsaturated polyester resin used in the present invention is a polyol component that is a mixture of a polyester polyol having unsaturated groups, a urethane catalyst, and a crosslinking agent for unsaturated groups (usually styrene monomer) (in addition to polyether polyol, etc. ) and an isocyanate component which is a mixture of isocyanate and peroxide. In the reaction, the polyol and isocyanate first form a urethane bond under the influence of a urethane catalyst, resulting in chain length extension. Then, under the influence of a peroxide catalyst,
The unsaturated group in the molecule and a crosslinking agent such as a styrene monomer undergo radical polymerization to form a highly crosslinked cured resin. Since all raw materials are of low molecular weight, the initial viscosity is low and easy to handle. Unless the liquid resin is heated to high temperatures, only the urethane reaction will proceed and the crosslinking reaction of unsaturated bonds will not occur. Since the urethane reaction can be controlled with a catalyst, thickening can be delayed for a long time. Even as the urethane reaction progresses and gradually increases in viscosity and loses its tackiness, it remains soft because it is diluted with styrene monomer, and when heated, it melts and then hardens for a long time. It can be thermoformed even after the lapse of time. The cured resin has better physical properties such as impact resistance and strength than ordinary unsaturated polyester, has less shrinkage during molding, and has heat resistance not found in polyurethane.
【0012】このウレタン変性不飽和ポリエステル樹脂
の加工性、物性の特徴を生かし、初期粘度が低い為ウレ
タンフォーム・ガラス繊維への含浸性が良く樹脂量が少
なくても充分含浸することから軽量化が可能で、熱硬化
性樹脂とガラス繊維との組み合わせによる補強材層であ
るため耐熱性があり寸法安定性が高く、取り付け方法に
制約はない。また芯材として伸びのある不織布を使用し
ているため、深絞り形状でも破れが生じることなく成形
することができ、デザインの自由度が高い。更にガラス
繊維は樹脂で含浸しているため飛散することはなく良好
な作業性で内装材基材を生産することができる。[0012] Taking advantage of the processability and physical properties of this urethane-modified unsaturated polyester resin, it has a low initial viscosity, so it has good impregnation into urethane foam and glass fiber, and even a small amount of resin can be sufficiently impregnated, resulting in weight reduction. Since it is a reinforcing material layer made of a combination of thermosetting resin and glass fiber, it is heat resistant and has high dimensional stability, and there are no restrictions on the mounting method. Furthermore, since a stretchy nonwoven fabric is used as the core material, it can be formed into a deep-drawn shape without tearing, providing a high degree of freedom in design. Furthermore, since the glass fibers are impregnated with resin, they do not scatter, and interior material base materials can be produced with good workability.
【0013】本発明の内装材基材の製法の一例を図2を
参照しながら説明する。
■ポリエチレンフィルムやポリプロピレンフィルムのよ
うな離型用フィルム(6)の上に、ウレタン変性不飽和
ポリエステル樹脂をドクターブレード(7)等で均一に
連続的に塗布し、その上にガラス繊維(2)を一定長さ
に切断して分散積層していく。その上面からはドクター
ブレード等により前記と同様に内側に樹脂(3)を塗布
した離型用フィルムを被せていき、ロール(8)等で全
体を均一に含浸させて得たプリプレグ(9)は巻取った
あと使用時に切断するか、或いは含浸直後製品形状に合
わせて切断してもよい。この時樹脂(3)を均一に塗布
する方法としてはスプレーで離型用フィルム(6)の上
に塗布してもよい。また樹脂(3)は全体で必要な量を
片側の離型用フィルム(6)のみに塗布して全体に含浸
させてもよい。
■プリプレグ(9)をセロファンフィルム(10)等で
密封して、スチレンモノマーの揮散を防止して20〜4
0℃の穏やかな条件で1日以上増粘させる。
■含浸樹脂を増粘させたプリプレグ(9)から離型用フ
ィルム(6)を取り除く
。■熱成形可能な不織布(1)の両面にプリプレグ(9
)を積層したものを、130〜160℃、好ましくは1
40〜150℃の熱プレス成形型(11)に挿入して0
.5〜3分、好ましくは0.5〜2分間熱プレス成形す
る。
■脱型して成形された内装材基材を得る。尚表皮は成形
後接着しても、成形時同時接着してもよい。これは表皮
の種類により調整する。An example of the method for manufacturing the interior material base material of the present invention will be explained with reference to FIG. ■Urethane-modified unsaturated polyester resin is uniformly and continuously applied with a doctor blade (7) on a release film (6) such as polyethylene film or polypropylene film, and then glass fiber (2) is applied on top of it. are cut to a certain length and distributed and stacked. A release film coated with the resin (3) on the inside is covered with a doctor blade or the like from above, and the entire prepreg (9) is uniformly impregnated with a roll (8) or the like. It may be wound up and then cut at the time of use, or it may be cut to match the product shape immediately after impregnation. At this time, the resin (3) may be applied uniformly onto the release film (6) by spraying. Alternatively, the resin (3) may be applied in a required amount to only one side of the release film (6) to impregnate the entire film. ■ Seal the prepreg (9) with cellophane film (10), etc. to prevent the volatilization of the styrene monomer.
Thicken for 1 day or more under mild conditions at 0°C. ■Remove the release film (6) from the prepreg (9) with thickened impregnated resin. ■Prepreg (9) on both sides of thermoformable nonwoven fabric (1)
) is laminated at 130 to 160°C, preferably 1
Insert into a hot press mold (11) at 40 to 150°C
.. Hot press molding is performed for 5 to 3 minutes, preferably 0.5 to 2 minutes. ■Remove the mold to obtain a molded interior material base material. The skin may be bonded after molding or may be bonded simultaneously during molding. This is adjusted depending on the type of epidermis.
【0014】[0014]
実施例1
ポリプロピレンフィルムの上に、ポリオール成分とイソ
シアネート成分とを混合したウレタン変性不飽和ポリエ
ステル樹脂を塗布量120g/m2となるようドクター
ブレードで均一に塗布しながら、ポリプロピレンフィル
ムを連続的に一定速度で移動させる。その上にガラス長
繊維のロービングをウレタンゴムのロールと30mm間
隔でナイフ刃を取り付けたロールとの間に挿入してこれ
らを回転させることにより30mm間隔に切断したガラ
ス繊維を連続的に供給し、80g/m2のガラス繊維を
ランダム方向に均一に分散積層させる。その上にポリプ
ロピレンフィルムを積層していき一定圧のプレスロール
で圧縮した後これをロール状に巻き取っていく。巻き取
ったロールはセロファンフィルムで密封して23℃で7
日間放置した。成形前にセロファンフィルムを取り除き
粘着性を失った上記プリプレグを製品長さに合わせて切
断し、裏表のポリプロピレンフィルムも取り除いた後、
アクリロニトリルと塩化ビニル(4:6)の共重合体を
ベースとする熱成形性を有する目付け量370g/m2
の不織布の両面にプリプレグを積層し、この積層品を1
50℃の成形天井用熱プレス成形型で一般肉厚2mmと
なるようプレス成形し、1分後脱型して770g/m2
の成形天井用基材を得た。Example 1 On a polypropylene film, a urethane-modified unsaturated polyester resin containing a polyol component and an isocyanate component was uniformly applied with a doctor blade to a coating amount of 120 g/m2, while the polypropylene film was continuously moved at a constant speed. to move it. On top of that, a roving of long glass fibers is inserted between a urethane rubber roll and a roll with knife blades attached at 30 mm intervals, and these are rotated to continuously supply glass fibers cut at 30 mm intervals, Glass fibers of 80 g/m2 are uniformly distributed and laminated in random directions. A polypropylene film is laminated on top of this, compressed with a press roll at a constant pressure, and then wound up into a roll. The wound roll was sealed with cellophane film and kept at 23℃ for 7 days.
I left it for days. The cellophane film was removed before molding, and the prepreg, which had lost its stickiness, was cut to match the length of the product, and the polypropylene film on the front and back sides was also removed.
Based on a copolymer of acrylonitrile and vinyl chloride (4:6) with thermoformability, basis weight 370g/m2
prepreg is laminated on both sides of the nonwoven fabric, and this laminated product is
Press molded with a heat press mold for molded ceilings at 50℃ to a general thickness of 2 mm, and removed from the mold after 1 minute to 770 g/m2
A base material for a molded ceiling was obtained.
【0015】[0015]
■本発明の方法で得られた内装材基材においては、強度
の高い樹脂とガラス繊維とを組み合わせた補強層と、多
孔質の不織布の芯材との構成からなるため、比較的軽量
で高い剛性がある。■The interior material base material obtained by the method of the present invention is composed of a reinforcing layer made of a combination of high-strength resin and glass fiber, and a core material of porous nonwoven fabric, so it is relatively lightweight and has a high cost. It is rigid.
【0016】
■本発明の方法で得られた内装材基材においては、耐熱
性の高い樹脂とガラス繊維とを組み合わせているため、
耐熱性があり、寸法安定性が非常に高い。[0016] Since the interior material base material obtained by the method of the present invention combines a highly heat-resistant resin and glass fiber,
It is heat resistant and has very high dimensional stability.
【0017】
■本発明の方法で得られた内装材基材においては、耐湿
性に優れた樹脂を用いているため、耐湿熱性が高い。(2) The interior material base material obtained by the method of the present invention has high moisture and heat resistance because a resin with excellent moisture resistance is used.
【0018】
■本発明の方法で得られた内装材基材においては、伸び
のある不織布材料を使用しているため、成形性が良くデ
ザインの自由度が高い。[0018] Since the interior material base material obtained by the method of the present invention uses a stretchable nonwoven fabric material, it has good moldability and a high degree of freedom in design.
【図1】本発明で得られた内装材基材の断面図である。FIG. 1 is a sectional view of an interior material base material obtained by the present invention.
【図2】本発明の製造方法の一例を示す説明図である。FIG. 2 is an explanatory diagram showing an example of the manufacturing method of the present invention.
1 熱成形可能な不織布
2 ガラス繊維
3 ウレタン変性不飽和ポリエステル樹脂4 芯材
層
5 補強用面材
6 離型用フィルム
7 ドクターブレード
8 ロール
9 プリプレグ
10 セロファンフィルム
11 熱プレス成形型1 Thermoformable nonwoven fabric 2 Glass fiber 3 Urethane-modified unsaturated polyester resin 4 Core layer 5 Reinforcing surface material 6 Release film 7 Doctor blade 8 Roll 9 Prepreg 10 Cellophane film 11 Hot press mold
Claims (1)
断してランダム方向に均一に分散したものにウレタン変
性不飽和ポリエステル樹脂を含浸させた後樹脂を穏やか
な条件で増粘させて表面の粘着性がなくなるまで熟成し
たものを、熱成形可能な繊維から作られる嵩高い不織布
の両面に積層し、熱プレス成形することにより硬化・一
体化することを特徴とする内装材基材の製造方法。Claim 1: The bundled long glass fibers are cut to a certain length and uniformly dispersed in random directions, and then impregnated with urethane-modified unsaturated polyester resin, and the resin is thickened under mild conditions to form a surface layer. A method for producing an interior material base material, which is characterized by laminating the material that has been aged until it loses its stickiness on both sides of a bulky nonwoven fabric made from thermoformable fibers, and curing and integrating the material by hot press molding. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2410841A JPH04216030A (en) | 1990-12-14 | 1990-12-14 | Manufacture of base material of interior material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2410841A JPH04216030A (en) | 1990-12-14 | 1990-12-14 | Manufacture of base material of interior material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04216030A true JPH04216030A (en) | 1992-08-06 |
Family
ID=18519936
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2410841A Withdrawn JPH04216030A (en) | 1990-12-14 | 1990-12-14 | Manufacture of base material of interior material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04216030A (en) |
-
1990
- 1990-12-14 JP JP2410841A patent/JPH04216030A/en not_active Withdrawn
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Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 19980312 |