JPH03161576A - Production of nubuck-tone artificial leather - Google Patents
Production of nubuck-tone artificial leatherInfo
- Publication number
- JPH03161576A JPH03161576A JP29555189A JP29555189A JPH03161576A JP H03161576 A JPH03161576 A JP H03161576A JP 29555189 A JP29555189 A JP 29555189A JP 29555189 A JP29555189 A JP 29555189A JP H03161576 A JPH03161576 A JP H03161576A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- fibers
- surface layer
- nonwoven fabric
- nubuck
- 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
Links
- 239000002649 leather substitute Substances 0.000 title claims abstract description 16
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 239000000835 fiber Substances 0.000 claims abstract description 91
- 238000000034 method Methods 0.000 claims abstract description 36
- 239000002344 surface layer Substances 0.000 claims abstract description 33
- 239000010410 layer Substances 0.000 claims abstract description 18
- 229920001971 elastomer Polymers 0.000 claims abstract description 12
- 239000000806 elastomer Substances 0.000 claims abstract description 12
- 230000001112 coagulating effect Effects 0.000 claims abstract description 4
- 239000004745 nonwoven fabric Substances 0.000 claims description 38
- 229920001410 Microfiber Polymers 0.000 claims description 22
- 229920000642 polymer Polymers 0.000 claims description 19
- 239000002131 composite material Substances 0.000 claims description 18
- 230000015271 coagulation Effects 0.000 claims description 9
- 238000005345 coagulation Methods 0.000 claims description 9
- 239000010985 leather Substances 0.000 claims 2
- 239000004744 fabric Substances 0.000 abstract description 5
- 238000000227 grinding Methods 0.000 description 15
- 239000012530 fluid Substances 0.000 description 9
- 239000013013 elastic material Substances 0.000 description 7
- 230000000704 physical effect Effects 0.000 description 7
- -1 polyethylene terephthalate Polymers 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000004952 Polyamide Substances 0.000 description 5
- 229920002647 polyamide Polymers 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000434 metal complex dye Substances 0.000 description 3
- 239000002861 polymer material Substances 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 206010022998 Irritability Diseases 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000003658 microfiber Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/007—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by mechanical or physical treatments
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/0043—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by their foraminous structure; Characteristics of the foamed layer or of cellular layers
- D06N3/0052—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by their foraminous structure; Characteristics of the foamed layer or of cellular layers obtained by leaching out of a compound, e.g. water soluble salts, fibres or fillers; obtained by freezing or sublimation; obtained by eliminating drops of sublimable fluid
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明はヌバック調として新規な人工皮革の製造方法に
関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for producing a novel artificial leather with nubuck texture.
[従来の技術]
従来、非常に緻密で短いナップを有する点に特徴のある
ヌバック調人工皮革を製造する方法としては、スエード
調人工皮革と同様に、織物、編物や不織布等のシートに
高分子弾性体等の樹脂を付与した後に表層部を研削し、
ナップを発現させて得る方法が一般に試みられている。[Prior Art] Conventionally, the method for producing nubuck-like artificial leather, which is characterized by extremely dense and short naps, involves applying polymer to a sheet of woven, knitted or non-woven fabric, similar to suede-like artificial leather. After applying resin such as elastic body, grind the surface layer,
Generally, methods for obtaining naps by expressing them have been attempted.
このような方法において、特に、短いナップを有するシ
ートは、高分子弾性体等の樹脂の付与量を単純に多くし
たり、あるいはチップの発現するシート面にコーティン
グ等の方法で樹脂を部分的に多く偏在させることにより
、該シートを構成する繊維の拘束を強くし研削での抵抗
を増すことにより得ることができるが、これらの方法で
は、高分子弾性体等の樹脂を多く必要とし、しかも樹脂
と繊維との直接の接着が形或されやすいのでシートの風
合が硬くなるという欠点がある。In this method, especially for sheets with short naps, the amount of resin such as polymeric elastomer applied may be simply increased, or the resin may be partially applied by coating the sheet surface where chips occur. By unevenly distributing a large amount of fibers, the fibers constituting the sheet can be more constrained and the resistance during grinding can be increased. However, these methods require a large amount of resin such as an elastic polymer, and the resin Since the direct adhesion between the fibers and the fibers tends to form, there is a disadvantage that the texture of the sheet becomes hard.
また、ナップを発現させる際の研削ペーパーのメッシュ
を細かくしたり、研削の処理回数を多くするなどの風合
を硬くしない手法も考えられるが、たとえ短いナップが
得られても、ヌバック調人工皮革の特徴である緻密なナ
ップは得られないという欠点がある。In addition, methods that do not make the texture hard, such as making the mesh of the grinding paper finer or increasing the number of grinding processes when creating naps, can be considered, but even if a short nap is obtained, nubuck-like artificial leather The disadvantage is that it is not possible to obtain the precise nap that is characteristic of .
一方、緻密なナップを得るために、一般的にはシートを
構成する繊維の密度を高くするという方法が考えられる
が、プレス等の手段で厚み方向にヘタリを与えて高い繊
維密度を得ても紙様の風合となってしまい、目的とする
皮革様の風合とはほど遠いものになる。On the other hand, in order to obtain a dense nap, it is generally possible to increase the density of the fibers that make up the sheet, but it is also possible to obtain a high fiber density by adding stiffness in the thickness direction by means such as pressing. The result is a paper-like texture, which is far from the desired leather-like texture.
また、加熱や繊維自身の改質等の手段でシートの収縮を
大きくして高繊維密度化をする方法も考えられるが、一
般に繊維密度が高いとシート風会は硬くなる傾向にあり
、緻密で短いナップと柔らかい風合との両立は十分では
なかった。Another possibility is to increase the shrinkage of the sheet by heating or modifying the fibers themselves to increase the fiber density, but in general, when the fiber density is high, the sheet texture tends to be hard and dense. It was not possible to achieve both a short nap and a soft texture.
[発明が解決しようとする課題]
本発明の目的は、上述したような点に鑑み、風合いを損
なうことなく、繊維密度が高く緻密で短いナップを有す
るヌバック調人工皮革を製造する方法を提供することに
ある。[Problems to be Solved by the Invention] In view of the above-mentioned points, an object of the present invention is to provide a method for manufacturing nubuck-like artificial leather having a high fiber density, dense and short naps without impairing the texture. There is a particular thing.
[課題を解決するための手段]
上述した目的を達成する本発明は、次の通りの構成を有
する。[Means for Solving the Problems] The present invention that achieves the above-mentioned objects has the following configuration.
すなわち、本発明のヌバック調人工皮革の製造方法は、
表層部の見掛け繊維密度が0.30g/d以上かつ空隙
率が70%以下である極細化可能な複合繊維からなる不
織布の主として表層部にある複合繊維から極細繊維を発
現させた後、該不織布に高分子弾性体を付与して該高分
子弾性体を乾式あるいは湿式で凝固せしめ、しかる後に
、該不織布の主として内層部を構成する複合繊維を極細
化することを特徴とする方法である。That is, the method for producing nubuck-like artificial leather of the present invention is as follows:
After developing microfibers mainly from the conjugate fibers in the surface layer of a nonwoven fabric made of conjugate fibers that can be made into ultrafine, the surface layer has an apparent fiber density of 0.30 g/d or more and a porosity of 70% or less. This method is characterized by applying an elastic polymer to the nonwoven fabric, coagulating the elastic polymer in a dry or wet process, and then ultrafine the composite fibers that mainly constitute the inner layer of the nonwoven fabric.
なお、かかる本発明のヌバック調人工皮革の製造方法に
おいて、好ましくは、極細繊維が、0.1デニール以下
の超極細繊維繊維であるものであり、あるいはまた好ま
しくは、高分子弾性体の凝固が乾式凝固方式の場合、該
高分子弾性体の付与量が15重量%以下であるものであ
り、あるいはまた好ましくは、高分子弾性体の凝固が湿
式凝固方式の場合、該高分子弾性体の付与量が100重
量%以下であるものである。In the method for producing nubuck-like artificial leather of the present invention, preferably, the ultrafine fibers are ultrafine fibers of 0.1 denier or less, or preferably, the coagulation of the polymeric elastic material is In the case of a dry coagulation method, the amount of the elastic polymer applied is 15% by weight or less, or preferably, when the coagulation of the elastic polymer is a wet coagulation method, the amount of the elastic polymer applied is 15% by weight or less. The amount is 100% by weight or less.
[作用コ 以下、さらに詳しく本発明について説明をする。[Action Co. The present invention will be explained in more detail below.
本発明では、繊維を立体的に絡合させた不織布において
、その表層部は繊維が高密度に絡合された繊維層を研削
することで緻密で短いナップを得て、一方、内層部にお
いては高分子弾性体を不織布を構成する繊維どうしを直
接接着することなく拘束させた状態で介在させることで
、柔軟な風合を得ることに特徴があるものである。In the present invention, in a nonwoven fabric in which fibers are three-dimensionally entangled, a dense and short nap is obtained in the surface layer by grinding the fiber layer in which the fibers are entangled with high density, while in the inner layer, It is characterized by the fact that a flexible texture is obtained by interposing an elastic polymer material in a state in which the fibers constituting the nonwoven fabric are restrained without being directly bonded to each other.
そして、本発明の方法は、かかる構造を得るために、緻
密な構造を持つ極細化可能な複合繊維からなる不織布を
用いて、特に2段階に分けた極細化処理と該不織布への
高分子弾性体の付与処理工程とをうまく組合わせて行な
って所期の目的を達成し得たものであり、まず、該緻密
な構造を持つ不織布の主として表層部にある複合繊維か
ら極細繊維を発現させた後、該不織布に高分子弾性体を
付与して該高分子弾性体を乾式あるいは湿式で凝固せし
め、さらに、その後に、該不織布の主として内層部を構
成する複合繊維を極細化するものである。In order to obtain such a structure, the method of the present invention uses a nonwoven fabric made of composite fibers that have a dense structure and can be made into ultra-fine fibers. The desired purpose was achieved by skillfully combining the process of adding body to the fabric, and first, ultrafine fibers were developed from the conjugate fibers mainly in the surface layer of the nonwoven fabric with a dense structure. After that, an elastic polymer material is applied to the nonwoven fabric, and the elastic polymer material is coagulated in a dry or wet process.Furthermore, the composite fibers that mainly constitute the inner layer of the nonwoven fabric are made extremely fine.
ここで表層部とは、主に繊維で構成され研削によりナッ
プを発現形成して、不織布表面となる部分であって、厚
みとしては研削の回数などの実用上の点で0.3M以下
であることが好ましい。Here, the surface layer is a portion that is mainly composed of fibers and forms naps by grinding to become the surface of the nonwoven fabric, and its thickness is 0.3M or less in practical terms such as the number of times of grinding. It is preferable.
すなわち、研削される表層部が高密度に繊維が絡合して
いる繊維層であると、繊維どうしの絡合が強いため、研
削する際の抵抗が大きく、その結果、ナップが短くなり
、かつ高密度に絡合されているために緻密なナップを得
ることができるのである。さらに、高分子弾性体の付与
前の表層部の状態としては、空隙率が小さいと、高分子
弾性体の占める割合いが少なくなって、製品では染色性
の差から繊維と高分子弾性体との色が互いに異なるイラ
ツキと称される品位上の欠点が生じることが少なくなり
、外観も良好で緻密なナップが得られるのである。In other words, if the surface layer to be ground is a fiber layer in which the fibers are entangled with each other at a high density, the entanglement of the fibers will be strong and the resistance during grinding will be large, resulting in short naps and Because they are highly entangled, a dense nap can be obtained. Furthermore, if the porosity of the surface layer before applying the polymeric elastic material is small, the proportion of the polymeric elastic material will decrease, and in products, due to the difference in dyeability, fibers and polymeric elastic material will be separated. This reduces the occurrence of a quality defect called irritability, where the colors of the napkins differ from each other, and it is possible to obtain a fine nap with a good appearance.
特に、空隙率を小さくする手段としては、加工での形態
保持や風合柔軟化を目的とした、あらかじめ高分子弾性
体と溶解性が異なっていて、後に溶出、除去し得る適宜
の高分子物質等を付与することなども考えられるが、こ
の場合では、繊維と高分子弾性体との接着が妨げられて
チップが長くなったり、緻密さに劣るため好ましくなく
、繊維を除いた一定以上の実質的な空隙率が必要である
。In particular, as a means to reduce the porosity, an appropriate polymeric material that has a different solubility from the polymeric elastomer and can be eluted and removed later is used for the purpose of maintaining shape and softening the texture during processing. However, in this case, it is undesirable because the adhesion between the fibers and the polymeric elastic body is hindered, resulting in longer chips and poor density. A suitable porosity is required.
このような観点から、本発明者らの知見によれば、極細
繊維を発現させる前の複合繊維からなる不織布の表層部
の状態として、繊維密度としては、0.30g/cd以
上であること、特に好ましくは0.35g/cnf以上
と高密度に絡合されていることが必要であって、かかる
高密度に絡合されている場合には、このような繊維層を
研削することで緻密で短いチップを得ることがで゛きる
のであり、かつ、そのときの表層部の空隙率としては7
0%以下であることが重要である。From this point of view, according to the findings of the present inventors, the state of the surface layer of a nonwoven fabric made of composite fibers before developing ultrafine fibers, the fiber density is 0.30 g/cd or more; Particularly preferably, it is necessary that the fiber layer is entangled at a high density of 0.35 g/cnf or more, and when the fiber layer is entangled at such a high density, it is possible to grind such a fiber layer to make it dense. It is possible to obtain short chips, and the porosity of the surface layer is 7.
It is important that it be 0% or less.
不織布の表層部、好ましくは不織布の表層部のみが、極
細繊維の高密度に絡合された構造のシートを得る方法は
、特に限定されないが、好ましくは極細化可能な複合繊
維からなる不織布を、加熱などの手段で収縮させて、さ
らにカレンダーロール等を用いて加熱プレスし表層部だ
けを、上述の通り、見掛け繊維密度が0.30g/cm
2以上かつ空隙率が70%以下であるように高密度化さ
せた後、その部分の複合繊維を極細化し、さらに高速の
流体流を衝突させそのエネルギーで表層部の極細繊維に
緻密な絡合を与える方法などを好ましく使用できる。The method for obtaining a sheet having a structure in which the surface layer of the nonwoven fabric, preferably only the surface layer of the nonwoven fabric, is highly densely entangled with ultrafine fibers is not particularly limited, but preferably a nonwoven fabric made of composite fibers that can be made ultrafine, Shrink it by heating or other means, and then heat press it using a calendar roll or the like so that only the surface layer has an apparent fiber density of 0.30 g/cm as described above.
After increasing the density so that the porosity is 2 or more and the porosity is 70% or less, the composite fibers in that part are made ultra-fine, and a high-speed fluid flow is collided with the fibers, which uses the energy to tightly entangle the ultra-fine fibers in the surface layer. It is preferable to use a method that gives
本発明者らの知見によれば、最も好ましくは、極細化可
能な複合繊維が後述するように海島型複合繊維および/
または混合紡糸複合繊維である不織布を、加熱または加
熱プレスなどの手段で収縮させて特に表層部を高密度化
させた後に、高速流体流のエネルギーで結合成分を破壊
、除去することにより該複合繊維の極細化を行なうとと
もに該高速流体流によって緻密な絡合化をも同時に行な
う方法がよい。According to the findings of the present inventors, the most preferably ultrafine composite fibers are sea-island composite fibers and/or sea-island composite fibers as described below.
Alternatively, a nonwoven fabric that is a mixed spun composite fiber is shrunk by heating or hot pressing to make the surface layer particularly dense, and then the bonding components are destroyed and removed using the energy of a high-speed fluid flow to produce the composite fiber. It is preferable to use a method in which the particles are made extremely fine and at the same time, dense entanglement is achieved by the high-speed fluid flow.
この場合、結合成分を溶解させる溶剤をコーティング等
の方法で付与させて、さらに緻密化し、高速流体流の衝
突エネルギーが内層部には及ばず、より有効に表層部の
みに消費される方法で緻密な極細繊維の絡合化を図るこ
ともできる。In this case, a solvent that dissolves the bonded components is applied by a method such as coating to further densify the material, and the collision energy of the high-speed fluid flow does not reach the inner layer, but is more effectively consumed only in the surface layer. It is also possible to entangle ultrafine fibers.
ここで高速流体流とは、液体や気体を加圧して小さい孔
径のノズル、スリットなどから噴射させて高速の流体流
とし、繊維質シートに衝突させてそのエネルギーで繊維
の絡合化を行なうもので、流体としては衝突エネルギー
の大きさや取扱いやすさから液体であることが好ましく
、最も好ましくは水が用いられる。Here, high-speed fluid flow refers to liquid or gas that is pressurized and injected from a nozzle or slit with a small hole diameter to create a high-speed fluid flow that collides with a fibrous sheet and uses the energy to entangle the fibers. The fluid is preferably a liquid from the viewpoint of the magnitude of collision energy and ease of handling, and water is most preferably used.
該液体などの流体流にかける圧力は、表層部の極細繊維
形成型繊維の結合成分を破壊、除去し、極細繊維化と緻
密な絡合の双方の作用ができるものであればよく、特に
限定されず、極細繊維形成型繊維の極細繊維化、発現し
た極細繊維の絡合のしやすさに応じて適宜選べばよいが
、一般には30 kg/arr〜2 0 0 kg/c
nfの範囲が好ましい。The pressure applied to the fluid stream, such as the liquid, may be any pressure that can destroy and remove the binding components of the ultrafine fiber-forming fibers in the surface layer, and have the effect of both forming ultrafine fibers and densely entangling them, and is not particularly limited. However, it may be selected as appropriate depending on the ease with which the ultrafine fiber-forming fibers are formed into ultrafine fibers and the developed ultrafine fibers are entangled, but it is generally 30 kg/arr to 200 kg/c.
A range of nf is preferred.
次に、不織布の内層部については、極細繊維どうしが直
接接着されることなく、高分子弾性体が繊維と繊維との
空隙や周囲に介在した状態下で極細繊維が拘束されてい
ることが必要であり、このような構造を呈することによ
り、物理的作用に対する寸法変化などの変形を抑えつつ
、該極細繊維にある程度の自由度を持たせることができ
て、シートに良好な風合と物性を同時に与えることが可
能になる。Next, regarding the inner layer of the nonwoven fabric, it is necessary that the ultrafine fibers are restrained in a state where the polymeric elastic material is interposed in the spaces between and around the fibers, without directly adhering the ultrafine fibers to each other. By exhibiting such a structure, it is possible to give the ultrafine fibers a certain degree of freedom while suppressing deformation such as dimensional changes due to physical effects, giving the sheet good texture and physical properties. It is possible to give them at the same time.
しかして、不織布の内層部において繊維と繊維との空隙
や繊維の周囲に高分子弾性体が介在して物理的作用に耐
え得る物性が発現される構造を形成させる高分子弾性体
による繊維どうしの拘束状態を実現する方法として、複
合繊維よりなる内層不織布部分に対し、該複合繊維の結
合成分を除去する前に高分子弾性体を付与し、その後、
結合成分を除去する方法を好ましく用いることができる
。Therefore, in the inner layer of the nonwoven fabric, the polymeric elastic material is present in the spaces between the fibers and around the fibers, forming a structure that exhibits physical properties that can withstand physical action. As a method for realizing a restrained state, a polymer elastic material is applied to the inner layer nonwoven fabric portion made of composite fibers before removing the binding component of the composite fibers, and then,
A method that removes bound components can be preferably used.
すなわち、上述の如く、流体流処理などによって、不織
布の主として表層部にある複合繊維から極細繊維を発現
させた後に、該不織布に高分子弾性体を付与して該高分
子弾性体を凝固せしめ、さらに、該不織布の主として内
層部を構或している複合繊維を極細化せしめる方法が用
いられるものである。That is, as described above, after developing ultrafine fibers from the composite fibers mainly in the surface layer of the nonwoven fabric by fluid flow treatment or the like, applying an elastic polymer to the nonwoven fabric and coagulating the elastic polymer, Furthermore, a method is used in which the composite fibers that mainly constitute the inner layer of the nonwoven fabric are made extremely fine.
該高分子弾性体の付与量は、風合い、物性のバランス等
から、また付与方法などに応じて適宜選択されればよい
。The amount of the polymeric elastomer to be applied may be appropriately selected depending on the balance of texture, physical properties, etc., and the application method.
たとえば、高分子弾性体の凝固方式が、乾式の場合には
、風合が硬くなりやすいので不織布を形或する繊維の重
量に対してその有効或分が15%以下であることが好ま
しく、最適には10%以下とするのが好ましいものであ
る。また、湿式の場合には、不織布を形成する繊維の重
量に対して100%以下であることが好ましく、最適に
は60%以下とするのが好ましいものである。For example, if the coagulation method of the polymer elastomer is a dry method, the texture tends to become hard, so it is preferable that the effective proportion is 15% or less with respect to the weight of the fibers forming the nonwoven fabric. The content is preferably 10% or less. Furthermore, in the case of a wet method, the amount is preferably 100% or less, most preferably 60% or less, based on the weight of the fibers forming the nonwoven fabric.
高分子弾性体の付与方法としては、シートの内層部にお
いて、繊維に自由度を持たせることができるように高分
子弾性体が繊維どうしをある程度拘束して、良好な風合
いの付与が可能になる方法であればよく、特に限定はさ
れないが、高分子弾性体の溶液、エマルジョンあるいは
分散液を含浸あるいはコーティング等の方法で付与した
後に、乾式あるいは湿式で凝固または固化する方法を適
宜用いることができる。The method of applying the elastic polymer is that the elastic polymer restrains the fibers to some extent so that the fibers can have a degree of freedom in the inner layer of the sheet, making it possible to impart a good texture. Any method may be used, and there is no particular limitation, but a method in which a solution, emulsion, or dispersion of a polymeric elastomer is applied by a method such as impregnation or coating, and then coagulated or solidified by a dry or wet method can be used as appropriate. .
本発明において、最終的に不織布を形成する極細繊維は
、しなやかな風合、ソフトなタッチの面で、その繊度は
0. 1デニール以下であることが好ましく、より好
ましくは0.05デニール以下であることである。In the present invention, the ultrafine fibers that ultimately form the nonwoven fabric have a supple texture, a soft touch, and a fineness of 0. It is preferably 1 denier or less, more preferably 0.05 denier or less.
該繊度が小さいと、不織布の密度が同じ場合では繊維ど
うしの絡合箇所が多くなり、物理的作用を受けた際の応
力分散が図れるだけでなく、緻密で短いナップが得られ
やすく好ましいのである。When the fineness is small, there are many points where the fibers become entangled with each other when the density of the nonwoven fabric is the same, which not only makes it possible to disperse stress when subjected to physical action, but also makes it easier to obtain a dense and short nap. .
極細化が可能な複合繊維としては、従来から知られてい
る極細繊維形成型の複合繊維、すなわち物理的作用を加
えること、あるいは結合成分を除去することなどにより
比較的容易に極細繊維が得られる海島型複合繊維、混合
紡糸複合繊維、あるいは剥離型複合繊維等の各種の複合
繊維を適宜用いることができる。Composite fibers that can be made ultra-fine include conventionally known ultra-fine fiber-forming conjugate fibers, in other words, ultra-fine fibers can be obtained relatively easily by applying physical action or removing binding components. Various conjugate fibers such as sea-island conjugate fibers, mixed spun conjugate fibers, and peelable conjugate fibers can be used as appropriate.
極細繊維は、繊維形戊能を有する高分子物質からなるも
のであれば各種のものを用いることができ、ナイロン6
、ナイロン66などのボリアミド、ポリエチレンテレフ
タレート、ポリブチレンチレフタレートなどのポリエス
テル、ポリエチェン、ポリプロピレンなどのポリオレフ
ィン、ポリアクリ口ニトリルなどの高分子物質を適宜用
いることができる。Various types of ultrafine fibers can be used as long as they are made of polymeric substances that have the ability to form fibers, such as nylon 6
, polyamides such as nylon 66, polyesters such as polyethylene terephthalate and polybutylene ethylene phthalate, polyolefins such as polyethylene and polypropylene, and polymeric substances such as polyacrylic nitrile.
また、極細繊維形成型複合繊維の結合成分あるいは溶解
除去成分としては、ポリエチレン、ボリスチレン、ポリ
プロピレンなどを用いることができる。Furthermore, polyethylene, boristyrene, polypropylene, etc. can be used as the binding component or the dissolving and removing component of the ultrafine fiber-forming conjugate fiber.
本発明の方法において、ナップを形或させる面の研削(
バフィング等による毛羽出し起毛)は、高分子弾性体の
付与後、内層の複合繊維の極細化後あるいは極細化前の
適宜の時点で行なわれる。In the method of the invention, grinding (
Fluffing and raising by buffing or the like is carried out at an appropriate time after the application of the polymeric elastomer and after or before making the inner layer conjugate fiber extremely fine.
なお、本発明において、不織布の表層部の見掛け繊維密
度の測定は、該不織布の表面から厚み0.3 mm以下
に薄《スライスして厚み、重量、日付を計り密度を算出
する方法によるものであり、以下の実施例では、厚み0
.3mmにスライスをして算出をした。In the present invention, the apparent fiber density of the surface layer of the nonwoven fabric is measured by a method in which a thin slice of 0.3 mm or less is sliced from the surface of the nonwoven fabric and the thickness, weight, and date are measured to calculate the density. Yes, and in the following examples, the thickness is 0
.. Calculations were made by slicing into 3 mm pieces.
また、空隙率の測定は、算出した見掛け繊維密度と該繊
維の比重から次式より算出する方法によるものである。The porosity is measured using the following formula from the calculated apparent fiber density and the specific gravity of the fiber.
空隙率(%)
=100−(見掛け繊維密度÷繊維の比重)XIO[l
[実施例]
以下、実施例によって本発明を具体的に説明するが、本
発明は、以下の実施例に限定されるものではない。Porosity (%) = 100 - (apparent fiber density ÷ fiber specific gravity) XIO [l
[Examples] Hereinafter, the present invention will be specifically explained with reference to Examples, but the present invention is not limited to the following Examples.
実施例1
3デニールの2戊分系海鳥型複合繊維(島成分:ポリア
ミド、30重量%、島本数36本:海成分:ボリスチレ
ン70重量%)をカット長約51mm、捲縮数約14山
/インチの繊維とした。Example 1 A 3-denier two-branched seabird-type composite fiber (island component: polyamide, 30% by weight, number of islands: 36: sea component: boristyrene 70% by weight) was cut to a length of about 51 mm and a number of crimps of about 14/ inch of fiber.
この繊維を用い、カード、クロスラッパーを通してウエ
ブを形成して二一ドルパンチ処理にて不織布を作った。Using this fiber, a web was formed by passing it through a card and a cross wrapper, and a nonwoven fabric was made by a twenty-one dollar punch process.
こうして得られた不織布は、目付が2 8 8 g/d
密度0.151g/adであった。The nonwoven fabric thus obtained has a basis weight of 288 g/d.
The density was 0.151 g/ad.
得られた不織布を熱水中で収縮させて、さらにカレンダ
ーロールを用いてプレスし、乾燥して目付が377g/
rrf、厚み1.1mm,密度0.343g/adのシ
ートを得た。The obtained nonwoven fabric was shrunk in hot water, further pressed using a calendar roll, and dried to a basis weight of 377 g/
A sheet having a thickness of 1.1 mm and a density of 0.343 g/ad was obtained.
このシートの一部について、スライスマシンを用いて表
面から薄くスライスして分析したところ、表層部の目付
が110g/rd、表層部の厚み0.3 mm、表層部
の密度0.368g/cu!、表層部の空隙率が65%
であった。When a part of this sheet was thinly sliced from the surface using a slicing machine and analyzed, the basis weight of the surface layer was 110 g/rd, the thickness of the surface layer was 0.3 mm, and the density of the surface layer was 0.368 g/cu! , the porosity of the surface layer is 65%
Met.
さらに、この不織布シートに対し、孔径が0.25mm
,ピッチが1 mmの小孔が一列に配列したノズルより
100kg/carの圧力をかけた高速水流の噴射処理
を行なった。Furthermore, for this nonwoven fabric sheet, the pore diameter is 0.25 mm.
A high-speed water jet was sprayed at a pressure of 100 kg/car from a nozzle in which small holes with a pitch of 1 mm were arranged in a row.
このシートにポリウレタン樹脂の水エマルジョンを含浸
付与し、シートの島成分ポリアミド重量に対し15%付
与させた。このシートをトリクロルエチレン中で浸漬、
絞液を繰返し海或分のボリスチレンを除去した後、#1
80メッシュのサンドペーパーで研削を繰返し研削深さ
0.05mmの研削を行ない繊維シートを得た。This sheet was impregnated with a water emulsion of polyurethane resin to give an amount of 15% based on the weight of the island component polyamide of the sheet. This sheet is immersed in trichlorethylene,
After repeated squeezing to remove a certain amount of polystyrene, #1
Grinding was repeated with 80 mesh sandpaper to a grinding depth of 0.05 mm to obtain a fiber sheet.
さらに、常圧で1:2型金属錯塩染料で染色して、得ら
れた繊維質シートは緻密で短いナップを有しかつしなや
かで柔らかい風合いを有するヌバック調人工皮革であっ
た。Furthermore, the fibrous sheet obtained by dyeing with a 1:2 type metal complex dye at normal pressure was a nubuck-like artificial leather having dense and short naps and a supple and soft texture.
実施例2
実施例1で得られた日付が377g/n{、厚み1.1
n++n,密度0.343g/cnfでかつ表層部の日
付が110g/rr?、厚み0.3mm,密度0.
368g/ad、空隙率が65%の繊維質シートを用い
て、ポリウレタンの10%ジメチルホルムアミドを含浸
して、不織布の島成分ポリアミド重量に対し60%付与
させ30℃の水中で凝固させた。Example 2 The date obtained in Example 1 was 377 g/n {thickness 1.1
n++n, density 0.343g/cnf and surface date 110g/rr? , thickness 0.3mm, density 0.
A fibrous sheet having a weight of 368 g/ad and a porosity of 65% was impregnated with 10% dimethylformamide of polyurethane to give it 60% of the weight of the island component polyamide of the nonwoven fabric, and coagulated in water at 30°C.
このシートを乾燥後、トリクロルエチレン中で浸漬、絞
液を繰返し海成分のポリスチレンを除去した後、#18
0メッシュのサンドペーパーで研削を繰返し研削深さ0
.05mmの研削をした。After drying this sheet, it was repeatedly dipped in trichlorethylene and squeezed to remove the sea component polystyrene.
Grinding is repeated with 0 mesh sandpaper until the grinding depth is 0.
.. Grinding was done by 0.5mm.
こうして得られたシートにさらに、常圧で1:2型金属
錯塩染料で染色した。こうして得られた繊維質シートは
緻密で短いチップを有しかつ柔らかい風合いを有する良
好なヌバック調人工皮革であった。The thus obtained sheet was further dyed with a 1:2 type metal complex dye at normal pressure. The fibrous sheet thus obtained was a good nubuck-like artificial leather having dense, short chips and a soft texture.
比較例1
実施例1で得られた日付が288g/rrf,密度0、
151g/adの不織布を用いて熱水中で収縮させ、さ
らにカレンダーロールを用いてプレスし、乾燥して日付
けが405g/m,厚み1.38mm,密度0. 2
9 3 g/adの不織布シートを得た。このシート
の一部をスライスマシンを用いて表面から薄くスライス
して分析したところ、表層部の目付が86g/rr?,
表層部の厚み0.29mm,表層部の密度0. 2
9 7 g/cul,表層部の空隙率7↓%であった。Comparative Example 1 The date obtained in Example 1 was 288 g/rrf, the density was 0,
A nonwoven fabric of 151 g/ad is shrunk in hot water, further pressed using a calendar roll, and dried to give a date of 405 g/m, a thickness of 1.38 mm, and a density of 0. 2
A nonwoven fabric sheet weighing 93 g/ad was obtained. When a part of this sheet was thinly sliced from the surface using a slicing machine and analyzed, the basis weight of the surface layer was 86 g/rr? ,
The thickness of the surface layer is 0.29 mm, and the density of the surface layer is 0. 2
97 g/cul, and the porosity of the surface layer was 7↓%.
このシートにポリウレタン樹脂の水エマルジョンを含浸
付与し、シートの島成分ポリアミド重量に対し15%付
与させた。This sheet was impregnated with a water emulsion of polyurethane resin to give an amount of 15% based on the weight of the island component polyamide of the sheet.
このシートをトリクロルエチレン中で浸漬、絞液を繰返
し、海成分のポリスチレンを除去した後、#180メッ
シュのサンドペーパーで研削を繰返して研削深さ0.0
5mmの研削を行ない、さらにシートを常圧で1:2型
金属錯塩染料で染色した。This sheet was repeatedly dipped and squeezed in trichlorethylene to remove the sea component polystyrene, and then ground repeatedly with #180 mesh sandpaper until the grinding depth was 0.0.
After 5 mm of grinding, the sheet was further dyed with a 1:2 type metal complex dye at normal pressure.
こうして得られた繊維質シートは、柔らかい風合を有す
るものの、実施例1、実施例2のものと比べて、品位の
点で粗くてかつ長いナップを有するものであり、ヌバッ
ク調とは異なり、むしろスエード調と言うべき人工皮革
であった。Although the thus obtained fibrous sheet has a soft texture, it is rougher and has longer naps in terms of quality than those of Examples 1 and 2, and is different from the nubuck texture. Rather, it was an artificial leather that could be described as suede-like.
[発明の効果]
以上述べた通り、本発明の製造方法によれば、風合を損
なうことなく緻密で短いナップを有するヌバック調人工
皮革が得られるものである。[Effects of the Invention] As described above, according to the manufacturing method of the present invention, nubuck-like artificial leather having a dense and short nap can be obtained without impairing the feel.
Claims (4)
以上かつ空隙率が70%以下である極細化可能な複合繊
維からなる不織布の主として表層部にある複合繊維から
極細繊維を発現させた後、該不織布に高分子弾性体を付
与して該高分子弾性体を乾式あるいは湿式で凝固せしめ
、しかる後に、該不織布の主として内層部を構成する複
合繊維を極細化することを特徴とするヌバック調人工皮
革の製造方法。(1) Apparent fiber density in the surface layer is 0.30g/cm^2
After developing ultrafine fibers from the conjugate fibers mainly in the surface layer of a nonwoven fabric made of conjugate fibers that can be ultrafine and have a porosity of 70% or less, a polymer elastomer is added to the nonwoven fabric and the polymer A method for producing nubuck-like artificial leather, which comprises coagulating an elastic body in a dry or wet process, and then ultrafine the composite fibers that mainly constitute the inner layer of the nonwoven fabric.
あることを特徴とする特許請求の範囲第(1)項記載の
ヌバック調人工皮革の製造方法。(2) The method for producing nubuck-like artificial leather according to claim (1), wherein the ultrafine fibers are ultrafine fibers of 0.1 denier or less.
分子弾性体の付与量が15重量%以下であることを特徴
とする特許請求の範囲第(1)項記載のヌバック調人工
皮革の製造方法。(3) The nubuck preparation according to claim (1), characterized in that the coagulation of the elastomer polymer is performed by a dry coagulation method, and the amount of the elastomer polymer applied is 15% by weight or less. Method of manufacturing leather.
分子弾性体の付与量が100重量%以下であることを特
徴とする特許請求の範囲第(1)項記載のヌバック調人
工皮革の製造方法。(4) The nubuck preparation according to claim (1), wherein the coagulation of the elastic polymer is performed by a wet coagulation method, and the amount of the elastic polymer applied is 100% by weight or less. Method of manufacturing leather.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1295551A JP2808748B2 (en) | 1989-11-14 | 1989-11-14 | Method for producing nubuck-like artificial leather |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1295551A JP2808748B2 (en) | 1989-11-14 | 1989-11-14 | Method for producing nubuck-like artificial leather |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03161576A true JPH03161576A (en) | 1991-07-11 |
| JP2808748B2 JP2808748B2 (en) | 1998-10-08 |
Family
ID=17822109
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1295551A Expired - Fee Related JP2808748B2 (en) | 1989-11-14 | 1989-11-14 | Method for producing nubuck-like artificial leather |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2808748B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH1060782A (en) * | 1996-08-20 | 1998-03-03 | Asahi Chem Ind Co Ltd | Synthetic leather |
| US6299977B1 (en) | 1997-08-29 | 2001-10-09 | Teijin Limited | Non-Woven fabric and artificial leather |
-
1989
- 1989-11-14 JP JP1295551A patent/JP2808748B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH1060782A (en) * | 1996-08-20 | 1998-03-03 | Asahi Chem Ind Co Ltd | Synthetic leather |
| US6299977B1 (en) | 1997-08-29 | 2001-10-09 | Teijin Limited | Non-Woven fabric and artificial leather |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2808748B2 (en) | 1998-10-08 |
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