JPH0120984B2 - - Google Patents
Info
- Publication number
- JPH0120984B2 JPH0120984B2 JP59254445A JP25444584A JPH0120984B2 JP H0120984 B2 JPH0120984 B2 JP H0120984B2 JP 59254445 A JP59254445 A JP 59254445A JP 25444584 A JP25444584 A JP 25444584A JP H0120984 B2 JPH0120984 B2 JP H0120984B2
- Authority
- JP
- Japan
- Prior art keywords
- layer
- thermoplastic resin
- appearance
- sheet
- sponge
- 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
Links
- 239000006260 foam Substances 0.000 claims description 17
- 239000004800 polyvinyl chloride Substances 0.000 claims description 15
- 238000007666 vacuum forming Methods 0.000 claims description 15
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 14
- 229920005992 thermoplastic resin Polymers 0.000 claims description 14
- 238000006116 polymerization reaction Methods 0.000 claims description 7
- 238000007639 printing Methods 0.000 claims description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 3
- 230000004927 fusion Effects 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 18
- 239000000463 material Substances 0.000 description 12
- 210000004027 cell Anatomy 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 238000000465 moulding Methods 0.000 description 9
- 239000004014 plasticizer Substances 0.000 description 7
- 239000003381 stabilizer Substances 0.000 description 7
- 239000004744 fabric Substances 0.000 description 5
- 239000000945 filler Substances 0.000 description 5
- 239000004604 Blowing Agent Substances 0.000 description 4
- NKWPZUCBCARRDP-UHFFFAOYSA-L calcium bicarbonate Chemical compound [Ca+2].OC([O-])=O.OC([O-])=O NKWPZUCBCARRDP-UHFFFAOYSA-L 0.000 description 4
- 229910000020 calcium bicarbonate Inorganic materials 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000004156 Azodicarbonamide Substances 0.000 description 3
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 3
- 235000019399 azodicarbonamide Nutrition 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 239000012263 liquid product Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- -1 phthalate ester Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011162 core material Substances 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
産業上の利用分野
本発明は起毛様の外観をもつ真空成形用スポン
ジシート、更に詳しくは、自動車内装部品を真空
成形で製造するに当りその表皮材として適用さ
れ、内装部品にバツクスキン調または高級織物様
の外観および触感を付与することができるスポン
ジシートに関する。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is applied to a vacuum forming sponge sheet having a brushed appearance, more specifically, it is applied as a skin material when manufacturing automobile interior parts by vacuum forming. This invention relates to a sponge sheet that can give parts the appearance and feel of a backskin or high-quality fabric.
従来技術と解決すべき問題点
自動車内装部品(例えばインストパツド、グロ
ーブリツド、ドアトリム、ピラー等)の表皮材と
して、天然皮革様の絞をもつ合成樹脂製のシート
やスポンジシートが用いられている。最近では、
居住性向上、商品性向上のため、あるいは豪華さ
やソフト感などの優れた触感、そして防眩性やク
ツシヨン性といつた安全性のため、高級織物やバ
ツクスキン、スエードといつた素材が用いられる
ようになつている。しかし、かかる素材はそれ自
体高価で、かつ耐久性が乏しく、しかも手貼加工
となるため工程が複雑化する。従つて、比較的安
価で且つ加工し易い合成樹脂製の素材で上記目的
性能を満足させることが望まれている。Prior Art and Problems to be Solved Synthetic resin sheets or sponge sheets with a natural leather-like texture are used as skin materials for automobile interior parts (for example, instrument pads, glove lids, door trims, pillars, etc.). recently,
Materials such as high-quality fabrics, backskin, and suede are being used to improve livability and marketability, as well as for superior tactile sensations such as luxury and softness, and safety such as anti-glare and cushioning properties. It's getting old. However, such materials are themselves expensive, have poor durability, and must be applied by hand, which complicates the process. Therefore, it is desired that the above objective performance be satisfied with a synthetic resin material that is relatively inexpensive and easy to process.
従来、起毛様の外観をもつ合成樹脂シートある
いはスエード様の合成皮革としては、例えばカレ
ンダー法やペースト塗布によつて発泡層を形成
し、該発泡層の表面に加熱ロールまたは熱保持体
上の加熱担体で熱融処理を行い、表面を融着除去
(これによつてスポンジ起毛層が形成)すること
により製造される、良品位の起毛様外観をもつも
のが知られている。そして、これを真空成形の表
皮材シートとして用いる場合、半硬質熱可塑性シ
ート層を裏打ちすることが提案されている。 Conventionally, synthetic resin sheets or suede-like synthetic leather with a raised appearance have been produced by forming a foam layer by, for example, a calendaring method or paste coating, and applying heat on a heating roll or heat carrier to the surface of the foam layer. It is known that the material has a high-quality nap-like appearance and is manufactured by carrying out a heat-fusion treatment on a carrier to remove the fusion from the surface (thereby forming a sponge nap layer). When using this as a vacuum-formed skin material sheet, it has been proposed to back it with a semi-rigid thermoplastic sheet layer.
しかしながら、上記発泡層は直径200〜500μの
球状セルからなる構造を有することから、その表
面を融着除去してもセル内の溶融面が光つてキラ
キラ感を呈し、さらに真空成形での延伸で発泡層
が著しく延伸され、外観上スエードや高級織物に
比べ著しく品位に欠けるものとなる。また上記ス
ポンジ起毛層形成の溶融温度と裏打シート層の適
正な真空成形温度とがほとんど同じ範囲にあるた
め、成形時に表面が溶融して劣つた外観の表皮し
か得られない。この場合、裏打シート層を軟質化
し成形温度を下げる方法が考えられるが、低温で
成形すると、成形物の形状保持性が低下し、さら
に成形加工性も劣り、シワ、ブリツジといつた不
良が発生するため、安定加工が困難となる。 However, since the above foam layer has a structure consisting of spherical cells with a diameter of 200 to 500 μm, even if the surface is fused and removed, the molten surface inside the cells will shine and give a sparkling appearance, and furthermore, it will not be possible to stretch during vacuum forming. The foam layer is significantly stretched, resulting in an appearance that is significantly lower in quality than suede or high-quality fabrics. Furthermore, since the melting temperature for forming the raised sponge layer and the appropriate vacuum forming temperature for the backing sheet layer are in almost the same range, the surface melts during forming, resulting in a skin with an inferior appearance. In this case, a method of softening the backing sheet layer and lowering the molding temperature may be considered, but molding at low temperatures reduces the shape retention of the molded product, and also deteriorates molding processability, resulting in defects such as wrinkles and bridging. This makes stable machining difficult.
更に、これらのスポンジシートはより高品位の
外観を得るため、通常の方法で雲柄や織柄のプリ
ントが施こされるが、それらはスポンジ起毛層の
表面に点状に印刷されるため、成形展開後はプリ
ント模様が不明瞭となつたり、展開率の高い所で
は汚れがついたように見えたり、はげたように見
えたりして品位の劣る外観しか得られない。 Furthermore, in order to obtain a higher-quality appearance, these sponge sheets are printed with cloud patterns or woven patterns using the usual method, but since these are printed in dots on the surface of the sponge nap layer, After molding and development, the printed pattern becomes unclear, and in areas where the development rate is high, it looks smudged or peeled off, resulting in a poor-quality appearance.
本発明者らは、かかる欠点を改善し、品位の高
いバツクスキン調の高級織物様に似た外観を呈す
る表皮材を堤供するため鋭意研究を進めた結果、
表面の融着除去および真空成形後のキラキラ感を
無くすため発泡層のセル形状について検討した
所、球状では叙上の通りキラキラ感が目立ち、そ
して柱状では成形後の展開率が高い所で毛が疎に
なつて見えるのに対し、楕円(特に縦長楕円)状
であればキラキラ感は消失し、かつ所望の起毛状
態が得られることを見出した。なお、かかる縦長
楕円において短径は200μ以下、好ましくは100〜
200μに設定されていることが適当で、短径があ
まり小さすぎると起毛感に欠け、また200μを越
えると球状および柱状の場合と同じ欠点が起生す
る傾向にあることが認められた。また、上記裏打
シート層の問題は、発泡層に別途設けるのではな
く、発泡層を非発泡シート層上に積層することで
解決することを見出した。 The inventors of the present invention have carried out extensive research in order to improve these drawbacks and provide a skin material that has an appearance similar to that of a high-quality backskin-like luxury fabric.
When considering the cell shape of the foam layer in order to remove surface adhesion and eliminate glitter after vacuum forming, we found that with the spherical shape, the sparkle was noticeable as mentioned above, and with the columnar shape, hairs formed in areas where the expansion rate after molding was high. It has been found that while it appears sparse, if it is shaped like an ellipse (particularly a vertically elongated ellipse), the sparkle disappears and the desired raised state can be obtained. In addition, the minor axis of such a vertically elongated ellipse is 200μ or less, preferably 100~
It was found that it is appropriate to set it to 200μ, and that if the short axis is too small, the fluffy feel will be lacking, and if it exceeds 200μ, the same defects as those of spherical and columnar shapes tend to occur. It has also been found that the above-mentioned problem of the backing sheet layer can be solved by laminating the foam layer on the non-foam sheet layer instead of providing it separately on the foam layer.
発明の構成と効果
即ち、本発明は、縦長楕円状のセル構造を有す
る熱可塑性樹脂発泡層(A)および熱可塑性樹脂非発
泡シート層(B)から成る真空成形用スポンジシート
において、上記熱可塑性樹脂発泡層(A)は平均重合
度1000〜4000のポリ塩化ビニルから成り、かつそ
の縦長楕円状セルの長径が短径の1.3倍以上で、
短径が200μ以下であり、その表面を熱融着処理
したものであつて、上記熱可塑性樹脂非発泡シー
ト層(B)は平均重合度1700〜3500のポリ塩化ビニル
からなることを特徴とする起毛様の外観をもつ真
空成形用スポンジシートを提供するものである。Structure and Effects of the Invention That is, the present invention provides a sponge sheet for vacuum forming comprising a thermoplastic resin foam layer (A) having a vertically elliptical cell structure and a thermoplastic resin non-foamed sheet layer (B). The resin foam layer (A) is made of polyvinyl chloride with an average degree of polymerization of 1000 to 4000, and the major axis of the vertically elongated ellipsoidal cells is 1.3 times or more the minor axis,
The short axis is 200μ or less, and the surface thereof is heat-sealed, and the thermoplastic resin non-foamed sheet layer (B) is made of polyvinyl chloride with an average degree of polymerization of 1700 to 3500. The present invention provides a sponge sheet for vacuum forming that has a nap-like appearance.
本発明における上記熱可塑性樹脂発泡層(A)(以
下、A層と称す)は、縦長楕円状のセル構造を有
することを特徴とする。当該縦長楕円状セルにお
いて、その長径が短径の1.3倍以上、好ましくは
1.3〜2.0倍、および短径が200μ以下、好ましくは
100〜200μに設定されていることが適当である。
かかるセル構造を有するA層は通常、熱可塑性樹
脂、可塑剤(フタル酸エステルなど)、金属塩安
定剤、有機発泡剤(アゾジカーボンアミドなど)、
充填剤(重炭酸カルシウムなど)および着色剤等
を適宜配合して得られるペーストゾル組成物(以
下、組成物Aと称す)から形成される。 The thermoplastic resin foam layer (A) (hereinafter referred to as layer A) in the present invention is characterized by having a cell structure in the shape of an elongated ellipse. In the vertically elongated elliptical cell, the major axis is 1.3 times or more the minor axis, preferably
1.3 to 2.0 times, and the minor axis is 200μ or less, preferably
It is appropriate to set it to 100 to 200μ.
The A layer having such a cell structure usually contains a thermoplastic resin, a plasticizer (such as a phthalate ester), a metal salt stabilizer, an organic blowing agent (such as azodicarbonamide),
It is formed from a paste-sol composition (hereinafter referred to as composition A) obtained by appropriately blending a filler (such as calcium bicarbonate) and a coloring agent.
上記熱可塑性樹脂としては、ポリエチレン、ポ
リプロピレン、ポリ酢酸ビニル、ポリ塩化ビニル
(PVC)等が適用できるが、特に車輌用の内装部
品として要求される耐久性やソフト感などから軟
質のPVCが適している。さらに発泡セルのコン
トロールといつた面からペースト加工による軟質
PVCが最も容易に用いることができる。また使
用されるPVCは、その(平均重合度)=1000〜
4000のものが使用可能であるが、真空成形時に起
毛様の外観を損なうことなく、かつ安定した形成
ができるためにはの範囲は1500〜3500が好適で
ある。 As the above thermoplastic resin, polyethylene, polypropylene, polyvinyl acetate, polyvinyl chloride (PVC), etc. can be used, but soft PVC is particularly suitable due to the durability and soft feel required for interior parts for vehicles. There is. In addition, the foam cells are controlled and the softness is achieved through paste processing.
PVC is the easiest to use. In addition, the PVC used is (average degree of polymerization) = 1000 ~
4,000 can be used, but a range of 1,500 to 3,500 is preferable in order to ensure stable formation without impairing the nap-like appearance during vacuum forming.
本発明における上記熱可塑性樹脂非発泡シート
層(B)(以下、B層と称す)は、A層の下地層を構
成し真空成形性に重要な役割を果す。かかるB層
として、PVC、ABS等の真空成形性良好なシー
トを採用しうるが、A層の溶融発泡条件(通常
200〜230℃)およびA,B二層積層にソフト感を
もたせる点を考慮すれば、高重合度のPVC(通常
P=1700〜3500)のシートが適当である。B層は
通常、上記高重合度のPVC、可塑剤、安定剤お
よび充填剤等を適宜配合して得られるゾル組成物
(以下、組成物Bと称す)から形成される。 The thermoplastic resin non-foamed sheet layer (B) (hereinafter referred to as B layer) in the present invention constitutes the base layer of A layer and plays an important role in vacuum formability. As the B layer, a sheet with good vacuum formability such as PVC or ABS can be adopted, but the melting and foaming conditions for the A layer (usually
200 to 230°C) and to impart a soft feel to the two-layer laminate of A and B, a sheet of PVC with a high degree of polymerization (usually P = 1700 to 3500) is suitable. Layer B is usually formed from a sol composition (hereinafter referred to as composition B) obtained by suitably blending the above-mentioned high polymerization degree PVC, a plasticizer, a stabilizer, a filler, and the like.
本発明に係る真空成形用スポンジシートは、上
記A層およびB層で構成されるが、必要に応じて
B層の下地層として通常の熱可塑性樹脂発泡層(C)
(以下、C層と称す)を設けてもよい。このC層
は、真空成形加工の安定化(加工性向上、ブリツ
ジ、ドローダウンの向上、成形後収縮の向上、B
層へのヒートムラ減少、成形後の型保持)、成形
物にクツシヨン感を付与するため、加えてA層、
B層からの可塑剤の移行や基材からの有害物質の
移行(特にウレタン樹脂注入発泡におけるアミン
系触媒などによる劣化)を防止するためといつた
目的から適用され、通常、=1500〜3500の
PVC、可塑剤、発泡剤および安定剤等を適宜配
合して得られるペーストゾル組成物(以下、組成
物Cと称す)から形成されてよい。なお、C層の
セル形状は特に制限なく、楕円状、球状あるいは
柱状のいずれであつてもよい。 The sponge sheet for vacuum forming according to the present invention is composed of the above-mentioned layer A and layer B, but if necessary, a normal thermoplastic resin foam layer (C) may be used as the base layer of layer B.
(hereinafter referred to as C layer) may be provided. This C layer stabilizes the vacuum forming process (improves processability, improves bridging, drawdown, improves shrinkage after molding,
In order to reduce heat unevenness in the layer, retain the mold after molding) and give a cushioned feel to the molded product, layer A,
It is applied for the purpose of preventing the migration of plasticizer from the B layer and the migration of harmful substances from the base material (especially deterioration caused by amine catalysts in urethane resin injection foaming).
It may be formed from a paste-sol composition (hereinafter referred to as composition C) obtained by appropriately blending PVC, a plasticizer, a blowing agent, a stabilizer, and the like. Note that the cell shape of the C layer is not particularly limited, and may be elliptical, spherical, or columnar.
以下、本発明スポンジシートの製造手順につい
て詳述する。 Hereinafter, the manufacturing procedure of the sponge sheet of the present invention will be explained in detail.
先ずベルトまたは工程紙などのキヤリア上
に、必要に応じて組成物Cを塗布しゲル化させ、
次いで組成物Bを塗布しゲル化させた上に組成物
Aを順次塗り重ねた後180〜230℃で1〜3分間加
熱処理を行い、組成物A(および必要に応じてC)
を溶融発泡させて上からA層およびB層(および
必要に応じてC層)から成る積層スポンジシート
を得る。この場合、A層の縦長楕円状セルは、組
成物Aを通常0.1〜0.5mm厚で塗布してから、その
ゾルがゾル化する直前もしくは同時において発泡
剤を分解せしめるよう安定剤を選定し、発泡をコ
ントロールすることにより得ることができる。こ
のように各組成物を塗り重ねた後溶融発泡させる
方法を採用すれば、容易に作業を行うことがで
き、しかも後の成形時に層間剥離等の不具合が生
じないので有利であり、また加工コスト面でも有
利である。なお、上記C層の設置にあつて、例え
ばA層およびB層から成る積層スポンジシートを
形成した後そのB層側に、予め作成した熱可塑性
発泡シートをラミネートするか、あるいは熱可塑
性未発泡シートをラミネートし未発泡のA層と同
時に発泡させる方法が採用されてもよい。 First, if necessary, composition C is applied onto a carrier such as a belt or process paper and gelled.
Next, Composition B was applied and gelled, and then Composition A was sequentially applied and heat treated at 180 to 230°C for 1 to 3 minutes to form Composition A (and C as necessary).
are melted and foamed to obtain a laminated sponge sheet consisting of layer A and layer B (and layer C if necessary) from above. In this case, for the vertically elongated ellipsoidal cells of layer A, composition A is usually applied to a thickness of 0.1 to 0.5 mm, and then a stabilizer is selected so that the foaming agent is decomposed immediately before or at the same time as the sol becomes sol. This can be achieved by controlling foaming. Adopting this method of melting and foaming after coating each composition is advantageous because the work can be done easily, and problems such as delamination do not occur during subsequent molding, and processing costs are low. It is also advantageous in terms of In addition, when installing the above C layer, for example, after forming a laminated sponge sheet consisting of layers A and B, a previously prepared thermoplastic foam sheet is laminated on the B layer side, or a thermoplastic unfoamed sheet is laminated on the B layer side. A method may be adopted in which the A layer is laminated and foamed simultaneously with the unfoamed A layer.
次に、上記積層スポンジシートのA層表面を
熱融着処理、例えば該表面にその溶融温度以上に
加熱した担体(上質紙など)を押圧せしめ、表面
を連続的に融着除去(はぎとり)して起毛様の外
観をもつ本発明のスポンジシートを得る。 Next, the surface of the layer A of the laminated sponge sheet is subjected to heat-fusion treatment, for example, a carrier (such as high-quality paper) heated to a temperature higher than the melting temperature is pressed onto the surface, and the surface is continuously fused and removed (stripped off). A sponge sheet of the present invention having a nap-like appearance is obtained.
更に必要に応じて、このスポンジシートにバ
ツクスキン調または高級織物様の外観をもたせる
ため、通常の方法(グラビア印刷、スクリーン捺
染など)でプリントを行う。しかしながら、通常
の方法ではA層面における微細多孔状の先端にプ
リントインキが付着し、このため真空成形後のプ
リントがまばらになつたり割れたりして外観を著
しく損ねることが少なくない。そこで、A層面を
濃色に調整した後フイルム伸度100%以上の塩化
ビニル、酢酸ビニル系のビヒクルおよび顔料とし
て10〜50PHR、好ましくは20〜40PHRの酸化チ
タンを含む淡色プリントインキをプリントすれ
ば、成形後も高級織物感やバツクスキン様の外観
を損なわないことがわかつた。 Furthermore, if necessary, in order to give this sponge sheet a bag skin-like appearance or a high-quality fabric-like appearance, printing is performed by a conventional method (gravure printing, screen printing, etc.). However, in the conventional method, printing ink adheres to the tips of the fine pores on the surface of the A layer, and as a result, the print after vacuum forming often becomes sparse or cracked, which significantly impairs the appearance. Therefore, after adjusting the A layer surface to a dark color, print with a light color printing ink containing a vinyl chloride or vinyl acetate vehicle with a film elongation of 100% or more and titanium oxide of 10 to 50 PHR, preferably 20 to 40 PHR as a pigment. It was found that even after molding, the feel of high-quality fabric and the appearance of backskin were not impaired.
このようにして得られる本発明スポンジシート
は比較的安価で、かつ容易に加工することがで
き、これを自動車内装部品の表皮材として用いる
ことにより、従来より要求されている居住性、商
品品質、安全性等を高めうることが認められる。 The sponge sheet of the present invention obtained in this manner is relatively inexpensive and can be easily processed, and by using it as a skin material for automobile interior parts, it can achieve the conventionally required comfort, product quality, and It is recognized that safety etc. can be improved.
次に実施例を挙げて本発明をより具体的に説明
する。 Next, the present invention will be described in more detail with reference to Examples.
実施例 1A層
(組成物A) 重量部
PVC(鐘渕化学工業(株)製のPSH26、=1700)
…100
可塑剤(DUP、新日本理化(株)製) …70
安定剤(Zn―Na系複合液状品) …3
発砲剤(アゾジカ―ボンアミド系) …2
充填剤(重炭酸カルシウム) …10
着色剤 …10B層
(組成物B) 重量部
PVC(三菱モンサント化成(株)製のP―470、
=3500) …100
可塑剤(DUP) …70
安定剤(Ba―Zn系複合液状品) …3
充填剤(重炭酸カルシウム) …20C層
(組成物C) 重量部
PVC(PSH26) …100
可塑剤(DUP) …70
安定剤(Ba―Zn系複合液状品) …3
充填剤(重炭酸カルシウム) …20
発泡剤(アゾジカーボンアミド系) …2
工程紙上に組成物C、組成物Bおよび組成物A
をそれぞれ0.2mm、0.5mmおよび0.2mmの厚みで順次
塗り重ね(ゲル化させ)、直ちに215℃にて2〜3
分間の加熱処理で同時に溶融発泡させて上からA
層、B層およびC層から成るスポンジシートを得
る。該シートのA層表面に、200〜230℃に加熱し
た担体(上質紙)を押圧せしめ、表面を融着除去
して起毛様の外観をもつ総厚1.5mmのスポンジシ
ートを得る。Example 1 Layer A (Composition A) Part by weight PVC (PSH26 manufactured by Kanebuchi Chemical Co., Ltd., = 1700)
…100 Plasticizer (DUP, manufactured by Shin Nihon Rika Co., Ltd.) …70 Stabilizer (Zn-Na composite liquid product) …3 Blowing agent (azodicarbonamide type) …2 Filler (calcium bicarbonate) …10 Coloring Agent...10 B layer (composition B) parts by weight PVC (P-470 manufactured by Mitsubishi Monsanto Chemical Co., Ltd.,
=3500) …100 Plasticizer (DUP) …70 Stabilizer (Ba-Zn composite liquid product) …3 Filler (calcium bicarbonate) …20 C layer (composition C) weight part PVC (PSH26) …100 Plasticizer Agent (DUP)...70 Stabilizer (Ba-Zn based composite liquid product)...3 Filler (calcium bicarbonate)...20 Blowing agent (azodicarbonamide based)...2 Composition C, Composition B and Composition A
0.2 mm, 0.5 mm, and 0.2 mm thick respectively (gelled) and immediately heated to 215℃ for 2 to 3 coats.
Melt and foam at the same time with heat treatment for 1 minute and then
A sponge sheet consisting of layer B and layer C is obtained. A carrier (high-quality paper) heated to 200 to 230°C is pressed onto the surface of layer A of the sheet, and the surface is fused and removed to obtain a sponge sheet with a total thickness of 1.5 mm and a raised appearance.
次に、かかる起毛様外観のスポンジシートに対
し、白色プリントインキ(酸化チタン40PHR)
と濃色プリントインキ(大日本インキ化学工業(株)
製のVGS、東洋インキ(株)製のTカラー)を調色
してGR法で高級織物調のプリントを施こす。得
られるスポンジシートを表皮材として用い、真空
成形しながらこれにウレタン樹脂を注入・発泡し
てインストパツドを作成する。また、上記表皮材
シートを真空成形し、これをコア材に接着するこ
とで所定のドアトリムやピラーを作成することが
できる。 Next, white printing ink (titanium oxide 40PHR) was applied to the sponge sheet with a brushed appearance.
and dark printing ink (Dainippon Ink Chemical Co., Ltd.)
VGS manufactured by Toyo Ink Co., Ltd., T color manufactured by Toyo Ink Co., Ltd.) are toned and a high-quality textile-like print is applied using the GR method. The resulting sponge sheet is used as a skin material, and urethane resin is injected and foamed into it while vacuum forming to create an instrument pad. Moreover, a predetermined door trim or pillar can be created by vacuum forming the skin material sheet and adhering it to a core material.
Claims (1)
発泡層(A)および熱可塑性樹脂非発泡シート層(B)か
ら成る真空成形用スポンジシートにおいて、上記
熱可塑性樹脂発泡層(A)は平均重合度1000〜4000の
ポリ塩化ビニルからなり、かつその縦長楕円状セ
ルの長径が短径の1.3倍以上で、短径が200μ以下
であり、その表面を熱融着処理したものであつ
て、上記熱可塑性樹脂非発泡シート層(B)は平均重
合度1700〜3500のポリ塩化ビニルからなることを
特徴とする起毛様の外観をもつ真空成形用スポン
ジシート。 2 熱可塑性樹脂非発泡シート層(B)の下地層とし
て熱可塑性樹脂発泡層(C)を設けた前記第1項記載
のスポンジシート。 3 熱融着処理後、得られる微細多孔性表面に20
〜40PHRの酸化チタンを含有するインキでプリ
ント加工を施すことによつて、バツクスキン調ま
たは高級織物様の外観を呈する前記第1項または
第2項記載のスポンジシート。[Scope of Claims] 1. A sponge sheet for vacuum forming comprising a thermoplastic resin foam layer (A) having a vertically elliptical cell structure and a thermoplastic resin non-foamed sheet layer (B), wherein the thermoplastic resin foam layer ( A) is made of polyvinyl chloride with an average degree of polymerization of 1,000 to 4,000, and the major axis of the vertically elongated elliptical cells is at least 1.3 times the minor axis, and the minor axis is 200μ or less, and the surface is heat-fused. A sponge sheet for vacuum forming having a raised appearance, characterized in that the thermoplastic resin non-foamed sheet layer (B) is made of polyvinyl chloride with an average degree of polymerization of 1,700 to 3,500. 2. The sponge sheet according to item 1 above, wherein the thermoplastic resin foam layer (C) is provided as a base layer of the thermoplastic resin non-foamed sheet layer (B). 3 After heat fusion treatment, the resulting microporous surface has 20
3. The sponge sheet according to item 1 or 2, which exhibits a buckskin-like or high-grade fabric-like appearance by printing with an ink containing ~40 PHR of titanium oxide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25444584A JPS61132332A (en) | 1984-11-30 | 1984-11-30 | Sponge sheet for vacuum molding having raised hair-shaped external appearance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25444584A JPS61132332A (en) | 1984-11-30 | 1984-11-30 | Sponge sheet for vacuum molding having raised hair-shaped external appearance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61132332A JPS61132332A (en) | 1986-06-19 |
JPH0120984B2 true JPH0120984B2 (en) | 1989-04-19 |
Family
ID=17265101
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25444584A Granted JPS61132332A (en) | 1984-11-30 | 1984-11-30 | Sponge sheet for vacuum molding having raised hair-shaped external appearance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61132332A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4962601A (en) * | 1972-10-18 | 1974-06-18 | ||
JPS5539450A (en) * | 1978-09-14 | 1980-03-19 | Meidensha Electric Mfg Co Ltd | State display input system |
JPS5912837A (en) * | 1982-07-13 | 1984-01-23 | 東洋鋼鈑株式会社 | Napping vinyl chloride metallic plate |
JPS59145136A (en) * | 1983-02-09 | 1984-08-20 | 日東電工株式会社 | Plastic composite sheet |
-
1984
- 1984-11-30 JP JP25444584A patent/JPS61132332A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4962601A (en) * | 1972-10-18 | 1974-06-18 | ||
JPS5539450A (en) * | 1978-09-14 | 1980-03-19 | Meidensha Electric Mfg Co Ltd | State display input system |
JPS5912837A (en) * | 1982-07-13 | 1984-01-23 | 東洋鋼鈑株式会社 | Napping vinyl chloride metallic plate |
JPS59145136A (en) * | 1983-02-09 | 1984-08-20 | 日東電工株式会社 | Plastic composite sheet |
Also Published As
Publication number | Publication date |
---|---|
JPS61132332A (en) | 1986-06-19 |
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