JPS6013550A - Manufacture of embossed laminate - Google Patents

Manufacture of embossed laminate

Info

Publication number
JPS6013550A
JPS6013550A JP58121254A JP12125483A JPS6013550A JP S6013550 A JPS6013550 A JP S6013550A JP 58121254 A JP58121254 A JP 58121254A JP 12125483 A JP12125483 A JP 12125483A JP S6013550 A JPS6013550 A JP S6013550A
Authority
JP
Japan
Prior art keywords
molded
foam
synthetic resin
laminate
lactams
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
JP58121254A
Other languages
Japanese (ja)
Other versions
JPH0411377B2 (en
Inventor
青木 正巳
高尾 敬子
隆 大橋
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.)
Bridgestone Corp
Original Assignee
Bridgestone 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 Bridgestone Corp filed Critical Bridgestone Corp
Priority to JP58121254A priority Critical patent/JPS6013550A/en
Publication of JPS6013550A publication Critical patent/JPS6013550A/en
Publication of JPH0411377B2 publication Critical patent/JPH0411377B2/ja
Granted legal-status Critical Current

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Landscapes

  • Laminated Bodies (AREA)
  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、合成樹脂発泡体の片面または両面に面材を熱
圧縮成型によシ積層一体化し、凹凸の鮮鋭なる形状を型
付けする積層体の製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a laminate in which a face material is integrally laminated on one or both sides of a synthetic resin foam by thermal compression molding, and a sharply uneven shape is formed.

従来よシ、合成樹脂発泡体の片面または両面に熱可塑性
樹脂のフィルム、レザー、織布、不絨布等を接着またF
i融着一体化し、凹凸状の模様を付与したコ層ないし3
層の積層体が、車両内装材、家具の材料、壁材、床材な
どとして使用されている。通常このような積層体は主に
高周波ウエルグー法によシ製造されているが、この方法
は、非常に高コストの特殊フオームを必要とすると共に
高価なウエルダーマシンを要して経済的に不利であυ、
さらには使用できる面材が塩化ビニル等に限定されるな
どの欠点を有していた。
Conventionally, thermoplastic resin films, leather, woven fabrics, non-woven fabrics, etc. are adhered to one or both sides of synthetic resin foam.
i-fusion bonded and integrated layer to 3 with an uneven pattern
Laminated bodies of layers are used as vehicle interior materials, furniture materials, wall materials, floor materials, etc. Normally, such laminates are manufactured mainly by the high-frequency welding method, but this method is economically disadvantageous because it requires a very high-cost special form and an expensive welding machine. Ah,
Furthermore, it has the disadvantage that the surface material that can be used is limited to vinyl chloride or the like.

これに対して、特殊な発泡性硬化樹脂を発泡体表面に塗
布したあと、熱圧縮して型付は成型する方法や、発泡体
表面に熱可塑性樹脂組成物を塗布した後産熱圧縮成型す
る方法が提案されている。
On the other hand, there are methods in which a special foamable curing resin is applied to the surface of the foam and then heat-compressed and molded, or a thermoplastic resin composition is applied to the surface of the foam and then hot compression molded. A method is proposed.

しかしながら前者は、発泡性硬化樹脂を発泡硬化させる
ために複雑な工程を必要とするうえ、塗布工程と警句は
工程とを連続して行なわなければならないという制約を
有していた。また、後者の方法は熱可塑性樹脂を用いる
ため、得られる製品が熱に対して可逆的に硬化−軟化を
繰シ返す性質を持ち、形状の安定性の点で劣るという欠
点を有していた。
However, the former method requires a complicated process in order to foam and harden the foamable curable resin, and has the restriction that the coating process and the curing process must be performed consecutively. In addition, since the latter method uses thermoplastic resin, the resulting product has the property of repeatedly curing and softening in response to heat, and has the disadvantage of poor shape stability. .

さらに、車両用内装材や家具の材料等に用いる積層材に
ついては、例えば鋭い角部や幅が連続的に変化する凹部
などの立体的な形状を鮮鋭に出すことが要求さhる場合
が多いが、上述した従来方法では所望する形状のものを
得ることが困難であった。
Furthermore, laminated materials used for vehicle interior materials and furniture materials are often required to have sharp three-dimensional shapes, such as sharp corners and recesses that continuously change width. However, with the conventional methods described above, it was difficult to obtain a desired shape.

本発明者等は上記事情に鑑み、コスト的に有利な熱圧縮
成型法が適用でき、しかも伺ら特殊なフオームや特殊な
工程を要することがなく、簡単かつ確実に合成樹脂発泡
体と面材とを所望の立体的診鋏を精度良く形成して積層
一体イヒし得る方法を開発すべく鋭意研究を実施した結
果、合成樹脂発泡体と面材とを、少なくともいずれか一
方の面にあらかじめラクタム類からなる層を形成した後
に積層、熱圧縮成形することにより、良好な成形後の形
状を得られることを見い出して本発明に至った。
In view of the above circumstances, the present inventors have realized that a cost-effective thermal compression molding method can be applied, and that it is possible to easily and reliably form synthetic resin foams and face materials without requiring special forms or special processes. As a result of conducting intensive research to develop a method that can form the desired three-dimensional diagnostic scissors with high precision and laminate them together, we found that the synthetic resin foam and the face material were pre-coated with lactam on at least one side. The inventors have discovered that a good shape after molding can be obtained by forming a layer consisting of the same material, laminating the same, and then hot compression molding, thereby leading to the present invention.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

本発明の型付は積層体の製造方法は、合成樹脂発泡体の
少なくとも型付けされるべき面に面材をいて、前記合成
樹脂発泡体の警句けされるべき面及びこの面に接して重
ね合わされる面材の面のうちのいずれか一方もしくは両
方に、積層に先だってラクタム類からなる層を形成して
おくととを特徴とする6゜ 本発明に用いられる合成樹脂発泡体としては、汎用のエ
ーテル系軟質ポリウレタンフォーム及びエステル系ポリ
ウレタンフォームが好適である。
The method for producing a molded laminate of the present invention includes providing a face material on at least the surface of the synthetic resin foam to be molded, and stacking the synthetic resin foam on the surface of the synthetic resin foam to be molded and in contact with this surface. 6. The synthetic resin foam used in the present invention is characterized in that a layer made of lactams is formed on one or both of the surfaces of the face material prior to lamination. Flexible polyurethane foams and ester polyurethane foams are preferred.

また、エーテル系ポリウレタン、エステル系ポリウレタ
ン等の発泡体原料に、熱融着性を高めるために塩化ビニ
ル樹脂や可塑剤等を添加して発泡させた発泡体、軟質ポ
リウレタンフォームに塩化ビニル樹脂ペースト、塩化ビ
ニ〃デン、樹脂ラテックス等を含浸させた発泡体、前記
発泡体原料に熱圧縮成型性向上剤(例えばアミノアルコ
ール類やラクタム類等)を添加して発泡させた発泡体等
を用いることもできる。
In addition, we also produce foams made by adding vinyl chloride resin, plasticizers, etc. to foam raw materials such as ether polyurethane and ester polyurethane in order to improve heat fusion properties, vinyl chloride resin paste on flexible polyurethane foam, Foams impregnated with vinylidene chloride, resin latex, etc., foams made by adding heat compression moldability improvers (for example, amino alcohols, lactams, etc.) to the foam raw materials, etc. may also be used. can.

貫た、ラクタム類としては、ε−カプロラクタム、γ−
ブチロラクタム、δ−バレロラクタム、エナントラクタ
ム、ドデカノラクタム等が使用でキ、/i−’Iε−カ
グロラクタムが好適である。上記ラクタム類は、単一種
または混合物として用いられ、また必要に応じて重合触
媒を添加して用いることもできる。この重合触媒として
は、ナトリウム、カリウム、リチウム、亜鉛、マグネシ
ウム、アルミニウム等の金属のアルコラード、フェノラ
ートや、前記金属の水酸化物、水素化物、酸化物及び炭
酸塩、前記金属の有機酸(例えば酢酸、プロピオン酸、
酪酸、ステアリン酸m> との塩類やイソシアネート類
、第3級アミン類などが適用できる。
The lactams include ε-caprolactam, γ-
Butyrolactam, δ-valerolactam, enantholactam, dodecanolactam, etc. are used, and /i-'Iε-caglolactam is preferred. The above-mentioned lactams may be used alone or as a mixture, and a polymerization catalyst may be added thereto if necessary. Examples of the polymerization catalyst include alcoholides and phenolates of metals such as sodium, potassium, lithium, zinc, magnesium, and aluminum, hydroxides, hydrides, oxides, and carbonates of the metals, and organic acids of the metals (such as acetic acid). , propionic acid,
Salts with butyric acid, stearic acid m>, isocyanates, tertiary amines, etc. can be used.

上記ラクタム類は、そのまま溶融して用いるか、あるい
は水、アルコール等のヒドロキシル成分やアミン、酸、
ヒドロキシルアミン等に溶解させた状態で用いられる。
The above-mentioned lactams can be used as they are by melting them, or they can be used with hydroxyl components such as water, alcohol, amines, acids, etc.
It is used in a state dissolved in hydroxylamine etc.

上記ラクタム類は、合成樹脂発泡体および/または面材
表面に層を形成するKあたって、l積層面(接合される
発泡体と面材との積層面)あたり、soy/−以上、よ
り好ましくは100−グo。
The above-mentioned lactams are more preferably soy/- or more per laminated surface (laminated surface of the foam and facing material to be joined) for forming a layer on the surface of the synthetic resin foam and/or facing material. is 100-g o.

t/−が用いられ、rot/−未満であると熱圧縮成型
による型付は性の改良効果が少なく1.また熱融着性も
十分に得られない。一方ゲo o f / m’を越え
ると型付は性及び熱融着性の効果は得られるものの、余
剰なラクタム類の基布への侵み出しなどが生じると共に
コスト的にも不利となシ、加えてフオーム表面が硬くな
って感触の悪化をまねくため好ましくない。発泡体表面
にラクタム類から・なる層を形成する場合には、ラクタ
ム類を発泡体内部に/mm以上浸透せしめることが好壕
しく、これにより確実な熱融着性及びが格tけVトを得
ることができる。
t/- is used, and if it is less than rot/-, molding by hot compression molding has little effect on improving properties; Further, sufficient heat fusion properties cannot be obtained. On the other hand, if the value exceeds 0 o f / m', although the effects of molding properties and heat fusion properties can be obtained, excess lactams may seep into the base fabric, and it is also disadvantageous in terms of cost. In addition, this is not preferable because the foam surface becomes hard, leading to a worsening of the feel. When forming a layer made of lactams on the surface of a foam, it is preferable to allow the lactams to penetrate into the foam by at least 1/2mm, thereby ensuring reliable thermal adhesion and excellent V-temperature. can be obtained.

一ルコータ一方式、スプレー方式、カーテンフローコー
タ一方式等を用いて各面に均一に塗工するか、あるいは
グラビアコータ一方式によ9点塗工する方法が好適であ
り、更に塗工後、塗工面にローラをかけること匠より、
発泡体等への浸透度を高めることができる。
It is preferable to uniformly coat each surface using a one-way coater, a spray method, a curtain flow coater, or the like, or to apply nine-point coating using a one-way gravure coater. From the craftsman, apply a roller to the coated surface.
The degree of penetration into foam etc. can be increased.

才た、用いる面倒の種類には%に制限はないが、凹凸形
状をもって成型する側に用いる表側面材としては、天然
繊維を織布もしくは不、織布としたもの、あるいは軟質
塩化ビニル樹脂、ポリアミド樹脂、ポリエステル樹脂、
アクリル樹脂、塩化ビニリデン樹脂等の合成樹脂を、フ
ィルム、レザー、織布もしくは不織布としたものが好適
に用いられ、更にこれらの材料に起毛あるいは植毛処理
を施し軸方向に/ 00%以上、好ましくusoo4以
上の伸び率をもち、200%モジュラスが侶。ゆ7cm
以下、好ましくは、t、 o kg/ 、以下のものが
望ましく、このような物性をもつ面材を用いることによ
シ、成型加工性を高めて明瞭で鮮鋭な凹凸形状をもった
積層成形品を得ることができる。かがる物性をもった面
材の好適な例としては、ウーリ’ナイロン織布をあげる
ことができる。
There is no limit to the type of material to be used, but the surface material used for the side to be molded with an uneven shape may be woven or non-woven natural fibers, soft vinyl chloride resin, polyamide resin, polyester resin,
Synthetic resins such as acrylic resins and vinylidene chloride resins are preferably used as films, leathers, woven fabrics, or non-woven fabrics, and these materials are further treated with raising or flocking so that the axial direction is 00% or more, preferably usoo4. It has a growth rate of 200% and a modulus of 200%. Yu7cm
Preferably, the following is t, o kg/, and by using a surface material having such physical properties, a laminate molded product with improved moldability and a clear and sharp uneven shape can be obtained. can be obtained. A suitable example of the surface material having the physical property of bending is Wooli' nylon woven fabric.

一方、凹凸形状に成形する会衆のない裏側面材としては
、前述の表側面材と同様のものや、レジンボード、ハー
ドボード、合板、木板、ダンボール板、金属板、合成樹
脂板等の剛性を有する板材が好適に用いられる。上記の
凹凸形状に成形する盛装のない面材としては、伸び率が
小さいものが適しておシ、特に伸び率、2%以下のもの
が好ましく、これによシ加工適性等に優れた積層成形品
を得ることができる。
On the other hand, as the back side material that is formed into an uneven shape and does not have a structure, it is possible to use the same material as the front side material mentioned above, resin board, hardboard, plywood, wood board, cardboard board, metal board, synthetic resin board, etc. A plate material having the following properties is preferably used. As the surface material without embellishment to be formed into the above-mentioned uneven shape, a material with a small elongation rate is suitable, and a material with an elongation rate of 2% or less is particularly preferable. You can get the goods.

なお、上記の面材は、熱圧縮成型に際して熱板に接する
ため、その熱板温度よ7シ10℃以上高い溶融温度をも
つものを選択することが好ましい。
In addition, since the above-mentioned face material comes into contact with the hot plate during thermal compression molding, it is preferable to select one having a melting temperature that is 7 to 10° C. higher than the hot plate temperature.

また、凹凸形状が不要な側に用いられる面材と発泡体と
の間の接着は、ラクタム類を塗布し熱圧縮して行なって
もよく、一般的な接着加工法、すなわち接着剤の塗工、
フレームラミネーション等により接着する方法も適用で
き、特に制限されるものではない。
In addition, adhesion between the face material and the foam used on the side where an uneven shape is not required may be done by applying lactams and heat compression. ,
Adhesion methods such as frame lamination can also be applied and are not particularly limited.

上記発泡体と面材とを積層、熱圧縮成型するにあたって
の条件及び用いる装置等は、特に制限されず、用いる材
料の物性等を考慮して適宜選定し得るが、圧縮温度とし
ては、用いるラクタム類の融点より高く、かつ熱板に接
触する面材の溶融温度よp10℃以上低い温度が好適で
あシ、さらに、使用する発泡体の耐熱温度の上限よシ低
温度であることが要求され、実際には;0−JμO℃程
度の温度範囲内で好ましい温度が選定される。
The conditions and equipment used for laminating and hot compression molding the above foam and face material are not particularly limited, and may be selected appropriately taking into consideration the physical properties of the materials used. The preferred temperature is higher than the melting point of the foam and at least 10°C lower than the melting temperature of the face material in contact with the hot plate.Furthermore, the temperature must be lower than the upper limit of the heat resistance temperature of the foam used. In practice, a preferable temperature is selected within a temperature range of approximately 0-JμO°C.

発泡体と面材との熱圧縮成型は、形付はロールまたは形
付はコンベアを用いて連続的に行なってもよく、ワるい
は熱プレス機によシパツチ式で行なうこともできる。更
に、本発明の方法においては、熱圧縮成型の型を取シ去
った後の積層体に、ラクタム類が、反応、硬化する前に
、ラクタム類の融点より低温度で前記型と同形状の鋳型
を嵌合させて押圧することによシ、凹凸形状の形くずれ
を確実に防止することができ、ラクタム類の塗工による
型付は性の向上と相俟って鮮鋭な形状をもった型付は積
層体を得ることができる。
The thermal compression molding of the foam and the facing material may be carried out continuously using a shaping roll or a shaping conveyor, or may be carried out in a batch manner using a mold or a hot press machine. Furthermore, in the method of the present invention, after the hot compression molding mold is removed, the lactams are added to the laminate in the same shape as the mold at a temperature lower than the melting point of the lactams, before reacting and hardening. By fitting and pressing the molds, it is possible to reliably prevent the uneven shape from deforming, and molding by coating with lactams improves the properties and gives a sharp shape. By molding, a laminate can be obtained.

なお、興味あるととに1本発明の方法によシ積層一体化
された発泡体と面材との間の接着層は、湿熱ないし熱環
境下に放置しておくと徐々に接着強度が増すことが判明
した。従って、本発明の方法によシ得られた型付は積層
体は、実際の使用にあたって発泡体と面材との間の接着
力の経時的劣化は起こシ難いものと思われる。
It is interesting to note that the adhesive layer between the foam and the face material, which are laminated together by the method of the present invention, gradually increases in adhesive strength when left in a moist heat or heat environment. It has been found. Therefore, it is considered that the molded laminate obtained by the method of the present invention is unlikely to suffer from deterioration of the adhesive force between the foam and the facing material over time during actual use.

以上、説明したように、本発明の型付は積層体の製造方
法によれば、発泡体、・および/lたは面材に設けたラ
クタム類の層が、熱圧縮成型に伴って反応、硬化し、発
泡体と面材との間の接着性を高めると共に優れた型付は
性を付与し、従って低い圧縮温度、短い圧縮時間の下で
も目標とする鮮鋭な凹凸形状を有する積層成型品が容易
かつ確実に得られると同時に、生産性も向上し、工程の
省エネルギー化にも寄与することができるという効果が
得られる。その上、型付は性の向上に伴って、従来の方
法では困難であった立体形状をもつ積層体の製造も可能
となシ、デザイン性の面についても工業上、実用上の価
値は非常に高いものである。
As explained above, according to the molding method of the present invention for producing a laminate, the lactam layer provided on the foam, /l or face material reacts with the hot compression molding. When cured, it improves the adhesion between the foam and the facing material, and excellent molding imparts properties, resulting in a laminate molded product that has the desired sharp uneven shape even under low compression temperatures and short compression times. can be obtained easily and reliably, and at the same time, the productivity is improved, and the effects can be achieved in that it can contribute to energy saving in the process. Furthermore, as the properties of molding have improved, it has become possible to manufacture laminates with three-dimensional shapes, which was difficult with conventional methods, and it has great industrial and practical value in terms of design. It is expensive.

次に実施例を示して本発明をさらに具体的に説明するが
、本発明は以下の実施例のみに限定されるものではない
EXAMPLES Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to the following Examples.

〔実施例1〕 第7図ないし第3図に示す形状の型を用いて第7表に示
す各材料によシ本発明の方法を適用した試料1.2.3
及びラクタム類を用いない比較試料1.2を成型した。
[Example 1] Sample 1.2.3 in which the method of the present invention was applied to each material shown in Table 7 using a mold having the shape shown in FIGS. 7 to 3.
Comparative sample 1.2 using no lactams was also molded.

熱圧縮条件は、各試料とも等しく、温度/グO℃、時間
5分間、圧力/J’Okg/cdとした。
The thermal compression conditions were the same for each sample: temperature/J'Okg/cd, time 5 minutes, and pressure/J'Okg/cd.

得られた各試料について、第1図に点P1、P2、P3
で示す型の部分に対応する部分の成形寸法な測定した。
For each sample obtained, points P1, P2, and P3 are shown in Figure 1.
The molding dimensions of the part corresponding to the part of the mold shown in were measured.

その結果を第1表中に示す。The results are shown in Table 1.

なお、理想寸法は点P1で2011点P2、P3で1o
tranである。
In addition, the ideal dimensions are 2011 points at point P1 and 1o at points P2 and P3.
It is tran.

第 l 表 第1表に示す寸法測定結果から分かるように、ラクタム
類としてε−カプロラクタムを塗布したものは、面材の
積層の有無にかかわらず理想寸法に近い成形寸法が得ら
れた。
Table 1 As can be seen from the dimensional measurement results shown in Table 1, molding dimensions close to ideal dimensions were obtained in the case of applying ε-caprolactam as the lactam, regardless of whether or not the face material was laminated.

なお、各試料について、型の第2図に範囲Aで示す部分
に和尚する部分の断面形状を調べたとこて、本発明の方
法を用いて得られた試料1.2゜3は、いずれも鮮鋭な
凹凸形状をもたせることができた。
For each sample, we examined the cross-sectional shape of the part shown in area A in Figure 2 of the mold, and found that all samples 1.2°3 obtained using the method of the present invention were It was possible to create a sharp uneven shape.

〔実施例2〕 第6図、第7図に示すまず目状の型を用いて積層体を成
型した。材料として、成形される表側面材を除いて同じ
材料を用いて実施例と比較例との2種類の積層体を得た
[Example 2] First, a laminate was molded using an eye-shaped mold shown in FIGS. 6 and 7. Two types of laminates, an example and a comparative example, were obtained using the same material except for the surface material to be molded.

表側面材を除く材料は以下のとおシである。The materials other than the surface material are as follows.

○裏側面材 ・木綿(伸び率:jチリ下1.200%モジュラス:切
断、織り:平織如) ○ラクタム類 ・ε−カプロラクタム ・塗工個所:発泡体の表側 ・塗工量:trof/n? ○発泡体 畢汎用ポリエーテル系ポリウレタンフォーム・密度:0
.020t/cr& 一一一′ また、熱圧縮条件は以下のとおシである。
○Back side material: Cotton (elongation rate: 1.200% modulus: cutting, weaving: plain weave) ○Lactams: ε-caprolactam ・Coating area: Front side of foam ・Coating amount: trof/n ? ○Foam: General-purpose polyether polyurethane foam・Density: 0
.. 020t/cr&111' The thermal compression conditions were as follows.

O温度 7μθ℃ 0時間 5分間 ○圧力 lグjkg/c11 用いた表側面材の種類及び物性は、第2表中に示したと
おシである。
Temperature: 7μθ°C 0 hours 5 minutes Pressure: lgjkg/c11 The type and physical properties of the surface material used are as shown in Table 2.

上記の材料及び熱圧縮条件のもとで得られた実施例及び
比較例の積層体について、第6図中に示す型の点Q1〜
Qzoに対応する部分の厚さを測定した結果、第2表に
示す値を得た。なお、寸法の理想値はすべてコoven
である。
Regarding the laminates of Examples and Comparative Examples obtained under the above-mentioned materials and hot compression conditions, the mold points Q1 to Q1 shown in FIG.
As a result of measuring the thickness of the portion corresponding to Qzo, the values shown in Table 2 were obtained. Please note that all ideal dimensions are for oven
It is.

第 2 表 第2表の寸法測定値から分かるように、実施例の積層体
は、比較例のものに比べて理想値にょシ近い値をもって
成型されている。これは、実施例のものが表側面材とし
て伸び率が充分大きく、かつコoO%モジュラスが二コ
に!g/mと充分小さいものを用いているため、型への
追従性が良いためと思われる。これに対して比較例の積
層体は、表側面材の伸び率が小さいため、成型時に型に
追従できず、所望の寸法が得られなかった。
Table 2 As can be seen from the measured dimensions in Table 2, the laminates of the examples were molded with values much closer to the ideal values than those of the comparative examples. This is because the elongation rate of the example is sufficiently large as a surface material, and the coO% modulus is 2! This seems to be due to the fact that it has good followability to the mold because it uses a sufficiently small g/m. On the other hand, in the laminate of the comparative example, since the elongation rate of the front side material was small, it could not follow the mold during molding, and the desired dimensions could not be obtained.

第g図には比較例の積層体の断面形状、第り図には実施
例の積層体の断面形状を示しであるが、比較例のものは
、面材の伸びが少なく肩部が引張られて鮮鋭な形状が得
られなかった、これに対して、実施例では充分に鮮鋭な
形状を得るととができた。
Figure g shows the cross-sectional shape of the laminate of the comparative example, and Figure 2 shows the cross-sectional shape of the laminate of the example. In contrast, in the Examples, a sufficiently sharp shape could be obtained.

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

第1図ないし第3図は実施例1において用いた型の形状
を示す図であって、第7図は底面図、第2図は第2図の
■−■線に沿う断面図、第3図は第7図の■−■線に沿
う断面図、第≠図は、実施例Iにおいて得られた試料の
要部断面図、第5図は同比較試料の要部断面図、第6図
、第7図は、実施例2において用いた型の形状を示す図
であって、第を図は底面図、第7図は第6図の■−■線
に沿う断面図、第r図は実施例2において得られた比較
例の積層体の要部断面図、第7図は同実施例の積層体の
要部断面図である。 第1図 第2図 第3図 第4図 第5図 第6図 第7図 肚=〒=■コf−=面 第8図 第9図 ec刀Zユ
1 to 3 are diagrams showing the shape of the mold used in Example 1, in which FIG. 7 is a bottom view, FIG. 2 is a sectional view taken along the line ■-■ in FIG. 2, and FIG. The figure is a cross-sectional view taken along the line ■-■ in Figure 7, Figure ≠ is a cross-sectional view of the main part of the sample obtained in Example I, Figure 5 is a cross-sectional view of the main part of the comparative sample, and Figure 6 , FIG. 7 is a diagram showing the shape of the mold used in Example 2, in which figure 7 is a bottom view, figure 7 is a sectional view taken along the line ■-■ in FIG. 6, and figure r is a FIG. 7 is a sectional view of a main part of a laminate of a comparative example obtained in Example 2, and FIG. 7 is a sectional view of a main part of a laminate of the same example. Fig. 1 Fig. 2 Fig. 3 Fig. 4 Fig. 5 Fig. 6 Fig. 7 Diagram 肚=〒=■kof-=face Fig. 8 Fig. 9 Fig. ec sword Zyu

Claims (1)

【特許請求の範囲】 l 合成樹脂発泡体の少なくとも型付けされるべき面に
面材を重ね合わせ、これら合成樹脂発泡体と面材とを所
望の凹凸形状を有する型に挾み込んで加熱、圧縮し、前
記合成樹脂発泡体と面相とを型付けすると共Kfi層一
層化体化行なう型付は積層体の製造方法において、前記
合成樹脂発泡体の型付けされるべき面及びこの面に接し
て重ね合わせられる面材の面のうちのいずれか一方もし
くは両方に、積層に先だってラクタム類からなる層を形
成しておくことを特徴とする型付は積層体の製造方法。 ユ 前記ラクタム類からなる層は前記合成樹脂発泡体と
面材との間の7層積層部についてj Og /lr?以
上である特許請求の範囲第7項記載の製造方法。 3 前記型付けされる面@は、伸び率が/ 00%以上
であp、roo%引張シ引張シラジュラスkg/cIf
L以下である特許請求の範囲第1項または第2m記載の
製造方法。
[Scope of Claims] l A face material is superimposed on at least the surface to be molded of the synthetic resin foam, and the synthetic resin foam and face material are sandwiched into a mold having a desired uneven shape and heated and compressed. However, when the synthetic resin foam and the surface are molded, the molding to form the Kfi layer into a single layer is performed in the method for manufacturing a laminate, in which the synthetic resin foam is molded on the surface to be molded and the surface is overlapped in contact with this surface. Molding is a method for producing a laminate, which is characterized by forming a layer made of lactams on one or both of the surfaces of the facing material prior to lamination. The layer consisting of the lactams has a 7-layer laminated portion between the synthetic resin foam and the facing material. The manufacturing method according to claim 7, which is the above. 3 The surface to be molded has an elongation rate of /00% or more, p, roo% tensile strength, tensile sillage kg/cIf
The manufacturing method according to claim 1 or 2m, which is less than or equal to L.
JP58121254A 1983-07-04 1983-07-04 Manufacture of embossed laminate Granted JPS6013550A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58121254A JPS6013550A (en) 1983-07-04 1983-07-04 Manufacture of embossed laminate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58121254A JPS6013550A (en) 1983-07-04 1983-07-04 Manufacture of embossed laminate

Publications (2)

Publication Number Publication Date
JPS6013550A true JPS6013550A (en) 1985-01-24
JPH0411377B2 JPH0411377B2 (en) 1992-02-28

Family

ID=14806704

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58121254A Granted JPS6013550A (en) 1983-07-04 1983-07-04 Manufacture of embossed laminate

Country Status (1)

Country Link
JP (1) JPS6013550A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02111715U (en) * 1989-02-25 1990-09-06

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02111715U (en) * 1989-02-25 1990-09-06

Also Published As

Publication number Publication date
JPH0411377B2 (en) 1992-02-28

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