JPH0314648A - High density fibrous structural article of polyamide and its production - Google Patents
High density fibrous structural article of polyamide and its productionInfo
- Publication number
- JPH0314648A JPH0314648A JP1316924A JP31692489A JPH0314648A JP H0314648 A JPH0314648 A JP H0314648A JP 1316924 A JP1316924 A JP 1316924A JP 31692489 A JP31692489 A JP 31692489A JP H0314648 A JPH0314648 A JP H0314648A
- Authority
- JP
- Japan
- Prior art keywords
- polyamide
- fabric
- fiber structure
- structural article
- 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.)
- Pending
Links
- 229920002647 polyamide Polymers 0.000 title claims abstract description 31
- 239000004952 Polyamide Substances 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000000835 fiber Substances 0.000 claims abstract description 52
- 239000004744 fabric Substances 0.000 claims abstract description 42
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- 230000008961 swelling Effects 0.000 claims abstract description 13
- 230000035699 permeability Effects 0.000 claims abstract description 10
- 239000005871 repellent Substances 0.000 claims description 5
- 229920002292 Nylon 6 Polymers 0.000 abstract description 7
- 230000005540 biological transmission Effects 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- 230000001846 repelling effect Effects 0.000 abstract 1
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 27
- 238000000034 method Methods 0.000 description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000007788 liquid Substances 0.000 description 10
- 235000019445 benzyl alcohol Nutrition 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000002131 composite material Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- 239000004677 Nylon Substances 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 238000009981 jet dyeing Methods 0.000 description 6
- 229920001778 nylon Polymers 0.000 description 6
- -1 polyethylene terephthalate copolymer Polymers 0.000 description 5
- 238000004043 dyeing Methods 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 206010061592 cardiac fibrillation Diseases 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000002600 fibrillogenic effect Effects 0.000 description 3
- 238000005111 flow chemistry technique Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- 229920001634 Copolyester Polymers 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 238000009940 knitting Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical group N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Woven Fabrics (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Multicomponent Fibers (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はポリアミドを用いた防水・i3 ’IW性を有
する高密度織維横造物に関する.
(従来の技術)
従来、防水性と透湿性を兼備した布帛を得る方法として
、ポリウレタン樹脂等を基布にコーティングする方法が
知られている(例えば特公昭60−47955号公報)
.
しかし、コーティング布帛を用いた衣料は蒸れ感が残留
し又、風合が硬いため用途が限定される.このため、布
帛の織編密度を高くした高密度布帛によりi3 ?’f
A防水性を得ることが提案されており、このような布帛
を得る方法として、フィブリル化(分割)可能な複合繊
維を用いて織物を製織した後、これを開繊分割し高密度
織物を得ることが知られている.
例えば特公昭61−9427号公報では、ポリアミドと
ポリエステルよりなる複合繊維を用いて編物を編或した
後、ポリアミド成分を薬剤にて膨潤せしめて復合繊維を
フィプリル化し、70℃以上の蒸熱で該編物の収縮を行
い高密度織物を得ることが開示されている。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a high-density woven fabric cross-structured material using polyamide and having waterproof and i3'IW properties. (Prior Art) Conventionally, as a method of obtaining a fabric having both waterproofness and moisture permeability, a method of coating a base fabric with a polyurethane resin or the like has been known (for example, Japanese Patent Publication No. 60-47955).
.. However, clothing using coated fabrics has a residual damp feeling and has a hard texture, which limits its uses. For this reason, i3? 'f
A: It has been proposed to obtain waterproof properties, and the method for obtaining such a fabric is to weave a fabric using composite fibers that can be fibrillated (split), and then split the fabric to obtain a high-density fabric. It is known. For example, in Japanese Patent Publication No. 61-9427, after knitting a knitted fabric using composite fibers made of polyamide and polyester, the polyamide component is swollen with a chemical to fibrillate the condensed fibers, and the knitted fabric is heated by steaming at 70°C or higher. It is disclosed that shrinkage is performed to obtain a dense fabric.
又、特開昭50−152094号公報には同じくポリア
ミドを含む剥離性の複合繊維を用いた繊維構造物にポリ
アミド威分の膨潤収縮剤を付与して、面積収縮率で10
〜70%、厚み増加率20〜350%、両者の比が2以
上に収縮させ絹様風合を有した繊維構造物を得ることが
記載されている。Furthermore, in Japanese Patent Application Laid-open No. 50-152094, a fiber structure using a peelable composite fiber containing polyamide is given a swelling and shrinking agent equivalent to the strength of polyamide, and the area shrinkage rate is 10.
It is described that a fiber structure having a silk-like texture can be obtained by shrinking the fiber structure by shrinking the fiber structure by 70%, the thickness increase rate by 20 to 350%, and the ratio of the two to 2 or more.
(発明が解決しようとする課題)
しかしながら、これら従来技術に開示されたものは何れ
もポリエステル等の非収縮或分を多量に含んだものであ
るため、高収縮せしめてもこれら成分のため厚地となり
衣料とすると用途が限定される問題点があった。(Problem to be Solved by the Invention) However, all of the materials disclosed in the prior art contain a large amount of non-shrinkable components such as polyester, so even if they are highly shrunk, these components make the fabric thick. When used as clothing, there was a problem that its uses were limited.
又、複合繊維を用いた前記高密度布帛は、フィブリル化
により細繊度となり、高密度化されやすくなるが通常の
収縮処理では未だ高密度化が足りず、充分な防水性・i
3湿性を得ることはできない。In addition, the high-density fabric using composite fibers becomes finer due to fibrillation, making it easier to increase the density, but ordinary shrinkage treatment is still insufficient for increasing the density, and sufficient waterproofness and i
3. Moisture cannot be obtained.
更に、収縮方法も単なる浸漬法しか開示されておらず、
単に膨潤剤への浸漬と薫熱処理を行っただけでは、特に
薄地布帛の場合、収縮斑が発生して、製品の外観・品位
を低下させる問題点があった.
本発明はかかる問題点を解決するものであって、高度の
防水性・i3湿性を有しながらしかも柔軟な風合を合わ
せ持つ高品位の繊維構造物を提供することを目的とする
ものである.
(ii題を解決するための手段)
本発明は、ポリアミド系繊維を用いた目付200g/m
t以下のmmraのみからなるものであって、表面がt
n水加工され、通気度0.5〜3cc/cm”秒、耐水
圧350mmH,○/am”以上、透湿度8000g/
m” ・24時間以上であるボリア壽ド高密度繊維構
造物であり、本発明方法は、ポリアミド系繊維を用いた
繊維構造物をポリアミド膨潤剤の溶液流中でWi環移動
せしめ、該繊維構造物を経方向及び緯方向に均一に10
%以上収縮させることを特徴とするものである。Furthermore, only a simple dipping method is disclosed as a shrinking method;
If the fabric is simply dipped in a swelling agent and subjected to heat treatment, shrinkage spots occur, especially in the case of thin fabrics, which deteriorates the appearance and quality of the product. The present invention is intended to solve these problems, and aims to provide a high-quality fiber structure that has a high degree of waterproofness and I3 moisture content, as well as a flexible texture. .. (Means for solving problem ii) The present invention uses polyamide fibers with a basis weight of 200 g/m.
It consists only of mmra less than t, and the surface is
n Water treated, air permeability 0.5-3cc/cm"sec, water pressure resistance 350mmH, ○/am" or more, moisture permeability 8000g/
The method of the present invention involves moving a fiber structure using polyamide fibers in a solution stream of a polyamide swelling agent, and moving the fiber structure in a solution flow of a polyamide swelling agent. 10 things uniformly in the longitudinal and latitudinal directions
% or more.
本発明に用いるポリアミドとしては、例えば、ナイロン
4.ナイロン6.ナイロン7.ナイロン11,ナイロン
12,ナイロン66,ナイロン610,ポリメタキシレ
ンアジパミド9ポリバラキシリレンデカンアミド.ポリ
ビスシクロへキシルメタンデカンアミド及びそれらを戒
分とするコポリアミドが挙げられるが、ナイロン6,ナ
イロン66が好ましい。Examples of the polyamide used in the present invention include nylon 4. Nylon6. Nylon7. Nylon 11, nylon 12, nylon 66, nylon 610, polymethaxylene adipamide 9 polyvaraxylylene decaneamide. Examples include polybiscyclohexylmethanedecaneamide and copolyamides containing them, with nylon 6 and nylon 66 being preferred.
これらポリアミドは、単独で紡糸して単糸織度0.5〜
8デニール程度の糸条となしてもよいが、他の易溶解性
ポリマー例えばアルカリに易溶解のポリエチレンテレフ
タレート共重合体等と複合紡糸して、後述の収縮処理前
に易溶解性ボリマーを溶解除去し、例えば0. 5デニ
ール以下のwA纏度糸となすことも可能である.
本発明の繊維構造物とは、織物.編物.不織布等を云う
。かかる繊維構造物は前記ポリアミド系繊維を用いたも
の、即ちポリアミ1゛系携維が全面に均一に存在するも
のである。該ポリアミド系繊維以外にはポリエステル,
綿,絹等の他繊維が若干量例えば高々30重量%程度混
用可能であるが、ポリアミド系繊維を全面に存在させる
ため、例えば織物で経糸又は緯糸にのみポリアミド系繊
維を用いるような混用方法は好ましくない。These polyamides are spun individually and have a single yarn weave of 0.5 to
It may be made into a yarn of about 8 denier, but it can be composite spun with other easily soluble polymers, such as polyethylene terephthalate copolymer, which is easily soluble in alkali, and the easily soluble polymer is dissolved and removed before the shrinkage treatment described below. For example, 0. It is also possible to use wA thread with a 5 denier or less. The fiber structure of the present invention is a woven fabric. knitting. Refers to nonwoven fabrics, etc. Such a fiber structure uses the polyamide fibers mentioned above, that is, polyamide 1 fibers are uniformly present over the entire surface. In addition to the polyamide fiber, polyester,
Although it is possible to mix a small amount of other fibers such as cotton or silk, for example up to 30% by weight, in order to have polyamide fibers present on the entire surface, mixing methods such as using polyamide fibers only in the warp or weft of textiles are not recommended. Undesirable.
又、繊維構造物の&Il織も種々のものが用い得るが、
織物の場合平織やツイル等の平坦なものが好ましい.更
に、繊維構造物は若干の立毛を有していてもよく、起毛
等の処理を行う場合は、以后の収縮処理に先立って該処
理を行う.
本発明の繊維構造物は、目付200g/m”以下の比較
的薄地のものである.又、本繊維構造物は城維層のみか
らなるもので、表面にウレタン等のコーティング層を有
するものや、フィルム等のラξネート層を有する多i構
遣のものとは異なる。In addition, various types of &Il weave can be used for the fiber structure, but
In the case of woven fabrics, flat ones such as plain weave or twill are preferred. Furthermore, the fibrous structure may have some napping, and when a treatment such as raising is performed, this treatment is performed prior to the subsequent shrinkage treatment. The fibrous structure of the present invention is relatively thin with a basis weight of 200 g/m or less.Furthermore, the fibrous structure may be made of only a fiber layer and may have a coating layer of urethane or the like on the surface. This is different from a multi-i structure having a ξ lanate layer such as a film or the like.
又、本繊維構造物は、表面が撥水加工されたものであり
(片面だけに限定されない)使用されるIn水剤には、
バーフルオル基を有するIR水剤、ボリシロキサンを主
戒分とするシリコン系l8水剤、主墳又は側鎖にアルキ
ル基を有する撥水剤又はそれらの混合物が含まれる。し
かしこれらに限定されるものではない.
更に、本繊維構造物は、通気度が0. 5〜3cc/c
m”−秒(JIS L−1096 (A法))である
.又、耐水圧は350mmH.○/cm”以上(JIS
L−1092 (A法))好ましくは500mmH
z ○/cm”以上但し通常は1 5 0 0 m m
Hz O / c m”以下であり、透湿度は800
0g/m” ・24時間以上(JIS L−109
9)但し、上限は10000g/m”24時間程度であ
る.
本繊維構造物は高密度にポリアミドが収縮したものであ
るが、カバファクター( 繊度(デニル)×打込本数(
本/インチ)〉の経方向,!!1方向の和が1800以
上程度で、特に経方向のカバファクターがl000以上
のものが好ましい.次に本発明方法について述べる。In addition, the surface of this fiber structure is water-repellent (not limited to only one side), and the In water agent used includes:
Included are IR water agents having a barfluoric group, silicone type 18 water agents containing polysiloxane as a main ingredient, water repellents having an alkyl group in the main or side chain, or mixtures thereof. However, it is not limited to these. Furthermore, this fiber structure has an air permeability of 0. 5~3cc/c
m"-second (JIS L-1096 (Method A)). Also, the water pressure resistance is 350mmH.○/cm" or more (JIS L-1096 (Method A)).
L-1092 (Method A)) Preferably 500mmH
z ○/cm" or more, but usually 1500 mm
Hz O/cm" or less, moisture permeability is 800
0g/m” ・24 hours or more (JIS L-109
9) However, the upper limit is about 10,000 g/m" for 24 hours. This fiber structure is made of highly densely shrunk polyamide, but it has a difference in coverage factor (fineness (denyl) x number of battings (
book/inch)〉longitudinal direction,! ! It is preferable that the sum in one direction is about 1800 or more, and in particular the hippofactor in the longitudinal direction is 1000 or more. Next, the method of the present invention will be described.
本発明で用いる繊維構造物は一般的な織物例えば経糸又
は緯糸の打込本数60〜180本/インチ程度、目付7
0〜180g/m”程度のものや、これに準ずる編物,
不織布等が用い得るが、特に目付70〜120g/m”
,更には70−100g/m’程度の薄地のものを用い
ると一層柔軟な風合が得られ好ましい.
次に本発明方法で用いるポリアミド膨潤剤としテハ、ベ
ンジルアルコール,フェノール, ギa,酢酸.ジメチ
ルホルムアミド.キシレン等のエマルジッンが挙げられ
、特にベンジルアルコールのエマルジョンが好ましい.
かかるボリア逅ド膨潤剤は従来用いられた1.5〜50
重量%程度の濃度で用いてもよいが、本発明の収縮処理
の場合浸漬法に比べ収縮作用がより進行するため、1〜
10重量%の低濃度溶液として用いることが好ましい.
又、本発明方法において、収縮率の調整は、このように
ポリア逅ド膨潤剤の濃度でコントロールする.かかるポ
リアミド膨潤剤のエマルジョン化に際しては、ノニオン
系,カチオン系,アニオン系又はこれらの混合型の界面
活性剤を添加して乳化分散させればよいが、本発明では
若干高め温度で溶液を用いることがあるため、アニオン
戒分を増強する等して高温域の乳化力を向上せしめた乳
化剤を用いることが好ましい.
本発明方法で重要なことは、収縮処理を経緯両方向に行
い、しかも全面に亘って.均一に行うことである.この
点に関し、従来用いられていたパディング法では連続処
理のため経方向の収縮が起こり難く又、浸漬法ではバッ
チ処理を行ったとしても、膨潤剤のポリアミド系繊維へ
の吸着が均一に起こらず本発明方法では用い得ない.
即ち、本発明方法では、被処理物を無張力下で均一に処
理できる液流処理装置を用いる.ここで液流処理装置と
は、無端状の被処理物を処理液と共に連続的な液流でV
Ii環移動せしめるもので、公知の液流染色機等がこれ
に当たる.
本発明方法はかかる液流処理装置を用いて前記ポリアミ
ド膨潤剤溶液からなる液流を生ぜしめ収縮処理を行うも
ので、ポリアミド膨潤剤?8液の液流を起こしつつこれ
を60〜100℃、好ましくは80〜100℃に昇温し
て1〜90分間、好ましくは20〜40分間程度処理す
るとよい。The fiber structure used in the present invention is a common fabric, for example, the number of warps or wefts is about 60 to 180 per inch, and the basis weight is 7.
0 to 180 g/m” or similar knitted fabrics,
Non-woven fabrics etc. can be used, especially those with a basis weight of 70 to 120 g/m"
Furthermore, it is preferable to use a thin material of about 70-100 g/m', as it will give a more flexible texture. Next, the polyamide swelling agents used in the method of the present invention include TE, benzyl alcohol, phenol, GA, acetic acid. Dimethylformamide. Examples include emulsions such as xylene, and benzyl alcohol emulsions are particularly preferred.
Such a boria-adsorbed swelling agent has a range of 1.5 to 50
Although it may be used at a concentration of about 1 to 1% by weight, since the shrinkage treatment of the present invention progresses more rapidly than the immersion method,
It is preferable to use it as a low concentration solution of 10% by weight.
Furthermore, in the method of the present invention, the shrinkage rate is controlled by the concentration of the polyamide swelling agent as described above. When emulsifying such a polyamide swelling agent, a nonionic, cationic, anionic, or mixed surfactant may be added to emulsify and disperse it, but in the present invention, the solution may be used at a slightly higher temperature. Therefore, it is preferable to use an emulsifier that has improved emulsifying power in the high temperature range by, for example, increasing the anion content. What is important about the method of the present invention is that the shrinkage treatment is performed in both directions, and moreover, over the entire surface. It should be done uniformly. Regarding this point, in the conventional padding method, shrinkage in the warp direction is difficult to occur due to continuous processing, and in the dipping method, even if batch processing is performed, the swelling agent does not adsorb uniformly to the polyamide fibers. It cannot be used in the method of the present invention. That is, the method of the present invention uses a liquid flow processing apparatus that can uniformly process the object under no tension. Here, the liquid flow processing device refers to an endless processing object that is processed by a continuous liquid flow along with a processing liquid.
This is a device that moves the Ii ring, such as a known liquid jet dyeing machine. The method of the present invention uses such a liquid flow processing device to generate a liquid flow consisting of the polyamide swelling agent solution to perform a shrinkage treatment. The temperature of the 8 liquids is raised to 60 to 100° C., preferably 80 to 100° C., and treated for 1 to 90 minutes, preferably 20 to 40 minutes while causing a liquid flow.
かかる処理で、繊維構造物を経方向及び緯方向に夫々1
0%以上、好ましくは15%以上収縮させる.収縮率が
10%未満では繊維間の絡合が不充分となり、均一な空
隙を有する,緻密な高密度繊維構造物とはならない.又
、収縮率は40%を超えるような極端に高密度なものも
製造可能であるが、かかるものはペーパライクであって
実用性は少ない.
尚、本発明方法で液流染色機を用いて収縮処理を行った
場合、該収縮処理前後に、被処理物を染色機に仕掛けた
まま精練や染色等の処理を連続して行うことが可能であ
る.
又、収iI1j!tの高密度繊維構造物には、公知のt
a水処理やシミリーカレンダー処理を施すと更に防水性
能が向上して好ましい.
斯かる本発明方法は前記の本発明繊維構造物を得るのに
適している.
(実施例)
実施例l
115D/72Fの6ナイロンマルチフィラメント糸を
経緯糸に用いて経119本/インチ.緯86本/インチ
の平織生機を得た.
得られた生機を液流染色機(日阪製作所タテ型サーキエ
ラ)に仕掛け、ベンジルアルコール5. 0%、乳化剤
(竹本油脂製KM−240)0.5%からなるエマルジ
ッン溶液で処理した.即ち、染色機を作動させて生機を
循環移動せしめつつ、エマルジョン溶液を30分間で8
0℃まで昇温し、このまま更に30分間処理を続けた後
、エマルジョン溶液を排出回収して水洗.乾燥し、経方
向に21%、緯方向に17%収縮せしめた高密度織物を
得た.かかる織物を撥水加工した後、185℃でシミリ
ー加工し透湿・防水布を得た.結果を第1表に示す.
実施例2
700/36Fの6ナイロンマルチフィラメント糸を経
糸に、ポリエヂレングリコールをl8モル重量%共重合
したポリエチレンテレフタレートと6ナイロンとよりな
り、繊維断面の中心から75重量部の8つの扇形部分の
6ナイロン(フィプリル化後0.18デニール)とこれ
を補完する.25重量部の共重合ポリエステルとが接合
した単糸横断面形状を有するloOD/50Fの複合繊
維を緯糸に用いて、経105本/インチ、緯77本/イ
ンチの平織生機を得た。With this treatment, the fiber structure is
Shrink it by 0% or more, preferably 15% or more. If the shrinkage rate is less than 10%, the entanglement between the fibers will be insufficient, and a dense, high-density fiber structure with uniform voids will not be obtained. It is also possible to manufacture extremely high-density materials with shrinkage rates exceeding 40%, but such materials are paper-like and have little practical use. In addition, when shrinkage treatment is performed using a jet dyeing machine according to the method of the present invention, it is possible to perform processes such as scouring and dyeing continuously before and after the shrinkage treatment with the object to be treated left in the dyeing machine. It is. Also, collection iI1j! For high density fiber structures of t, known t
aWater treatment or smear calender treatment is preferred as it further improves waterproof performance. Such a method of the present invention is suitable for obtaining the above-mentioned fiber structure of the present invention. (Example) Example 1 6 nylon multifilament yarn of 115D/72F was used for the warp and warp yarns, and the warp was 119 yarns/inch. A plain weave gray machine with a weft of 86 threads/inch was obtained. The obtained greige was placed in a liquid jet dyeing machine (Hisaka Seisakusho vertical type Cirquiera), and benzyl alcohol was added 5. 0% and an emulsifier (KM-240, manufactured by Takemoto Yushi Co., Ltd.) 0.5%. That is, while operating the dyeing machine and circulating the gray fabric, the emulsion solution was mixed in 8 minutes in 30 minutes.
After raising the temperature to 0°C and continuing the treatment for another 30 minutes, the emulsion solution was drained and collected and washed with water. A high-density fabric was dried and shrunk by 21% in the warp direction and 17% in the weft direction. After the fabric was water-repellent treated, it was subjected to shimmy treatment at 185°C to obtain a moisture-permeable and waterproof fabric. The results are shown in Table 1. Example 2 Made of 700/36F 6 nylon multifilament yarn as warp, polyethylene terephthalate copolymerized with 18 mol weight % of polyethylene glycol, and 6 nylon, 8 fan-shaped sections of 75 parts by weight from the center of the fiber cross section 6 nylon (0.18 denier after fibrillation) and complement this. A plain weave gray fabric having a warp of 105 pieces/inch and a weft of 77 pieces/inch was obtained using a loOD/50F composite fiber having a single yarn cross-sectional shape bonded with 25 parts by weight of copolyester as the weft yarn.
得られた生機を2重量%苛性ソーダを含む水溶液100
℃中で60分間処理をして共重合ポリエステル部分を溶
解した後、液流染色機を用いて、ベンジルアルコール濃
度8%、昇温温度9a℃で実施例l同様に処理して、経
26%、緯19%収縮せしめ高密度織物を得た.かかる
織物を撥水加工後、185℃でシミリー加工し、i3湿
・防水布を得た.結果を第l表に示す。The obtained gray fabric was dissolved in an aqueous solution containing 2% by weight of caustic soda.
℃ for 60 minutes to dissolve the copolymerized polyester portion, and then treated in the same manner as Example 1 using a jet dyeing machine at a benzyl alcohol concentration of 8% and a heating temperature of 9a℃ to obtain a dye with a diameter of 26%. , a high-density fabric with 19% weft shrinkage was obtained. This fabric was treated to be water repellent and then subjected to stain treatment at 185°C to obtain an i3 wet/waterproof fabric. The results are shown in Table I.
比較例1
実施例1で用いた生機を、ベンジルアルコール20%の
エマルジッン溶戒95℃に1分間浸漬して経33%、緯
25%収縮せしめ高密度織物を得た.かかる織物をta
水加工.シミリー加工した結果を第l表に示す.
通常の浸漬処理を行ったものは、表面に収縮斑が見られ
、所々充分に収縮していない箇所が存在し、第1表に示
す如く、耐水圧も低いものであっ実施例3
70d/32rの6ナイロンマルチフィラメント糸を経
糸に、ポリエチレングリコールを18モル重量%共重合
したポリエチレンテレフタレートと6ナイロンとよりな
り、繊維断面の中心がら75重量部の4つの扇形部分の
6ナイロンとこれを補完する25重量部の共重合ポリエ
ステルとが接合した単糸横断面.形状を有するfood
/50fの複合繊維を緯糸に用いて、経159本/イン
チ、緯80本/インチの綾織生機を得た.得られた生機
を2重量%苛性ソーダーを含む水溶液100℃中で60
分間処理をしてポリエステル部分を溶解した後立毛処理
を施し、液流染色機ヲ用いて、ベンジルアルコール6.
0%、’FL 化剤(竹本油脂製KM−240)0.
6%からなるエマルジョン溶液を30分間で98℃まで
昇温し、このまま更に30分間処理を続けた後、エマル
ジョン溶液を排出回収して水洗い、乾燥し経方向に21
%、緯方向に16%収縮せしめた高密度織物を得た.か
かる織物を染色ta水加工した後、185℃でシミリー
加工し、i3 ?W防水布を得た。Comparative Example 1 The gray fabric used in Example 1 was immersed in 20% benzyl alcohol at 95° C. for 1 minute to shrink by 33% in the warp and 25% in the weft to obtain a high-density fabric. Such a fabric is ta
Water processing. The results of shimmy processing are shown in Table I. Those that were subjected to the normal immersion treatment had shrinkage spots on the surface, some areas where the shrinkage was not sufficient, and as shown in Table 1, the water pressure resistance was low.Example 3 70d/32r The warp is made of nylon 6 multifilament yarn, which is made of nylon 6 and polyethylene terephthalate copolymerized with 18 mol weight percent polyethylene glycol, and is supplemented with nylon 6 in four fan-shaped sections of 75 parts by weight from the center of the fiber cross section. Cross section of a single yarn joined with 25 parts by weight of copolymerized polyester. food with shape
A twill loom with a warp of 159 yarns/inch and a weft of 80 yarns/inch was obtained by using composite fibers of /50 f as weft yarns. The obtained gray cloth was heated at 60°C in an aqueous solution containing 2% by weight of caustic soda at 100°C.
After processing for a minute to dissolve the polyester part, a napping process is applied, and using a jet dyeing machine, benzyl alcohol 6.
0%, 'FL forming agent (Takemoto Yushi KM-240) 0.
The temperature of the emulsion solution consisting of 6% was raised to 98°C in 30 minutes, and the treatment was continued for another 30 minutes.The emulsion solution was then discharged and collected, washed with water, dried, and heated for 21 minutes in the warp direction.
%, and a high-density fabric with 16% shrinkage in the weft direction was obtained. After dyeing and water-processing such a fabric, it is shimmy-processed at 185°C, and the i3? A W waterproof fabric was obtained.
結果を第2表に示す。The results are shown in Table 2.
実施例4
7 0 d/3 6 fの6ナイロンマルチフィラメン
ト糸を経糸に、ポリエチレングリコールを18モル重量
%共重合したポリエチレンテレフタレートと6ナイロン
とよりなり、繊維断面の中心から75重量部の8つの扇
形部分の6ナイロン(フィブリル化後0.l8デニール
)とこれを補完する25重量部の共重合ポリエステルと
が接合した単糸緯断面形状を有する1 0 0 ti/
5 0 fの複合繊維を緯糸に用いて、経105本/イ
ンチ、Il77本/インチの平織生機を得た.
得られた生機を実施例lと同様に苛性ソーダー処理,立
毛処理を施し、液流染色機を用いてベンジルアルコール
濃度8%昇温温度98℃で処理して、経26%緯19%
収縮せしめ高密度織物を得た。かかる織物を染色!8水
加工後、185℃でシミリー加工し、遇湿防水布を得た
。結果を第2表に示す。Example 4 The warp was made of polyethylene terephthalate copolymerized with 18 mol weight % of polyethylene glycol and 6 nylon, and 70 d/3 6 f 6 nylon multifilament yarn was used as the warp. 1 0 0 ti/ having a single yarn weft cross-sectional shape in which the fan-shaped part of nylon 6 (0.l8 denier after fibrillation) is joined with 25 parts by weight of copolymerized polyester to complement it.
A plain weave gray fabric with a warp of 105 yarns/inch and an Il of 77 yarns/inch was obtained using a 50 f composite fiber as the weft. The obtained gray cloth was treated with caustic soda and raised in the same manner as in Example 1, and treated using a jet dyeing machine at a benzyl alcohol concentration of 8% and a heating temperature of 98°C.
A shrunken, high-density fabric was obtained. Dye the fabric! 8 After water treatment, shimmy treatment was performed at 185°C to obtain a damp waterproof fabric. The results are shown in Table 2.
比較例2
実施例1で用いた生機を、2重量%苛性ソーダーを含む
水溶液100℃中で60分間処理して共重合ポリエステ
ル部分を溶解した後、立毛処理を施し、かかる織物を染
色・fJ3水加工したあと、185℃でシくり一加工し
た.結果を第2表に示す.
実施例5
実施例1,2のベンジルアルコールtN ’fXを第3
表の如く変化させて透温・防水布の引裂強力を測定した
.
第 3 表
第3表の如く、ベンジルアルコールの濃度にょり引裂強
力は変化し、収縮率が変化していることがわかる.実施
例1のものの場合、収縮率が上昇すると繊維間の遊びが
少なくなり引裂強力が低下するため、4%前後の濃度が
最も好ましく、実施例2のものの場合、収縮により溶解
戒分の空隙が埋められて引裂強力が上昇するが、更に収
縮率を上げる(ベンジルアルコール濃度を上げる〉と実
施例lのものと同様引裂強力が低下するので6〜8%の
濃度が最も好ましい.
(発明の効果)
以上の如く、本発明に係る繊維構造物は充分な防水性と
透湿性を有し、柔軟な風合と相俟って外衣用素材として
極めて有用なものである.又、本発明方法によれば、防
水性・i3?W性を兼備え更に柔軟な風合を有した高密
度繊維構造物が得られ、かかる繊維構造物はシワやシミ
として現れる収縮斑のない高品位な高密度繊維構造物が
得られる.
更に、本発明方法は、収縮率も自由にコントロール可能
であるため広汎な用途に応じ種々の素材を提供できる極
めて有用なものである。Comparative Example 2 The gray fabric used in Example 1 was treated in an aqueous solution containing 2% by weight of caustic soda at 100°C for 60 minutes to dissolve the copolyester portion, and then subjected to a napping treatment, and the fabric was dyed and treated with fJ3 water. After processing, it was processed at 185℃. The results are shown in Table 2. Example 5 The benzyl alcohol tN'fX of Examples 1 and 2 was added to the third
The tear strength of the heat permeable/waterproof fabric was measured with the changes shown in the table. Table 3 As shown in Table 3, it can be seen that the tear strength changes and the shrinkage rate changes depending on the concentration of benzyl alcohol. In the case of Example 1, as the shrinkage rate increases, the play between fibers decreases and the tear strength decreases, so a concentration of around 4% is most preferable. Although the tear strength increases due to filling, if the shrinkage rate is further increased (increasing the benzyl alcohol concentration), the tear strength decreases as in Example 1, so a concentration of 6 to 8% is most preferable. (Effects of the invention) ) As described above, the fiber structure according to the present invention has sufficient waterproofness and moisture permeability, and together with its soft texture, it is extremely useful as a material for outer clothing. According to the above, a high-density fiber structure having both waterproofness and i3?W properties and a soft texture can be obtained, and such a fiber structure is a high-quality high-density fiber without shrinkage spots that appear as wrinkles or stains. A structure is obtained.Furthermore, the method of the present invention is extremely useful in that it can provide a variety of materials for a wide range of uses because the shrinkage rate can be freely controlled.
Claims (2)
以下の繊維層のみからなるものであって、表面が撥水加
工され、通気度0.5〜3cc/cm^2秒、耐水圧3
50mmH_2O/cm^2以上、透湿度8000g/
m^2・24時間以上であるポリアミド高密度繊維構造
物。(1) Fabric weight 200g/m^2 using polyamide fiber
It consists only of the following fiber layers, the surface is water-repellent, the air permeability is 0.5-3cc/cm^2 seconds, and the water pressure resistance is 3.
50mmH_2O/cm^2 or more, moisture permeability 8000g/
Polyamide high-density fiber structure with a durability of m^2・24 hours or more.
ド膨潤剤の溶液流中で循環移動せしめ、該繊維構造物を
経方向及び緯方向に均一に 10%以上収縮させることを特徴とするポリアミド高密
度繊維構造物の製造方法。(2) A fiber structure using polyamide fibers is circulated in a solution stream of a polyamide swelling agent, and the fiber structure is uniformly shrunk by 10% or more in the warp and weft directions. A method for producing a dense fiber structure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1316924A JPH0314648A (en) | 1989-03-27 | 1989-12-06 | High density fibrous structural article of polyamide and its production |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7589689 | 1989-03-27 | ||
JP1-75896 | 1989-03-27 | ||
JP1316924A JPH0314648A (en) | 1989-03-27 | 1989-12-06 | High density fibrous structural article of polyamide and its production |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0314648A true JPH0314648A (en) | 1991-01-23 |
Family
ID=26417059
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1316924A Pending JPH0314648A (en) | 1989-03-27 | 1989-12-06 | High density fibrous structural article of polyamide and its production |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0314648A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012219422A (en) * | 2011-04-13 | 2012-11-12 | Komatsu Seiren Co Ltd | Method for producing fiber fabric and fiber fabric |
JP2015132043A (en) * | 2015-04-07 | 2015-07-23 | 小松精練株式会社 | Method for producing fiber fabric and fiber fabric |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57117647A (en) * | 1981-01-14 | 1982-07-22 | Kanebo Ltd | High densty flat fabric and method |
JPS6183370A (en) * | 1984-09-28 | 1986-04-26 | 東レ株式会社 | Production of spun like bulky cloth |
JPS61146840A (en) * | 1984-12-21 | 1986-07-04 | 帝人株式会社 | Knitted fabric for shielding ultraviolet rays and its production |
JPS63235572A (en) * | 1987-03-19 | 1988-09-30 | 東レ株式会社 | Special water resistant knitted article |
-
1989
- 1989-12-06 JP JP1316924A patent/JPH0314648A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57117647A (en) * | 1981-01-14 | 1982-07-22 | Kanebo Ltd | High densty flat fabric and method |
JPS6183370A (en) * | 1984-09-28 | 1986-04-26 | 東レ株式会社 | Production of spun like bulky cloth |
JPS61146840A (en) * | 1984-12-21 | 1986-07-04 | 帝人株式会社 | Knitted fabric for shielding ultraviolet rays and its production |
JPS63235572A (en) * | 1987-03-19 | 1988-09-30 | 東レ株式会社 | Special water resistant knitted article |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012219422A (en) * | 2011-04-13 | 2012-11-12 | Komatsu Seiren Co Ltd | Method for producing fiber fabric and fiber fabric |
JP2015132043A (en) * | 2015-04-07 | 2015-07-23 | 小松精練株式会社 | Method for producing fiber fabric and fiber fabric |
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