JPS636671B2 - - Google Patents
Info
- Publication number
- JPS636671B2 JPS636671B2 JP19372281A JP19372281A JPS636671B2 JP S636671 B2 JPS636671 B2 JP S636671B2 JP 19372281 A JP19372281 A JP 19372281A JP 19372281 A JP19372281 A JP 19372281A JP S636671 B2 JPS636671 B2 JP S636671B2
- Authority
- JP
- Japan
- Prior art keywords
- woven
- fluff
- fibers
- convex portion
- special
- 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
- 239000004744 fabric Substances 0.000 claims description 19
- 239000000835 fiber Substances 0.000 claims description 19
- 229920000728 polyester Polymers 0.000 claims description 9
- 239000000654 additive Substances 0.000 claims description 7
- 239000012670 alkaline solution Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229920001410 Microfiber Polymers 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- -1 Mg and Ca Chemical class 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000006068 polycondensation reaction Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 206010061592 cardiac fibrillation Diseases 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 230000002600 fibrillogenic effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- RZXLPPRPEOUENN-UHFFFAOYSA-N Chlorfenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C=C1 RZXLPPRPEOUENN-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
- 239000001639 calcium acetate Substances 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
- 235000011092 calcium acetate Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 210000001724 microfibril Anatomy 0.000 description 1
- MXXDSLLVYZMTFA-UHFFFAOYSA-N octadecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 MXXDSLLVYZMTFA-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- KBAFDSIZQYCDPK-UHFFFAOYSA-M sodium;octadecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCS([O-])(=O)=O KBAFDSIZQYCDPK-UHFFFAOYSA-M 0.000 description 1
- HRQDCDQDOPSGBR-UHFFFAOYSA-M sodium;octane-1-sulfonate Chemical compound [Na+].CCCCCCCCS([O-])(=O)=O HRQDCDQDOPSGBR-UHFFFAOYSA-M 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Landscapes
- Treatment Of Fiber Materials (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Description
【発明の詳細な説明】
本発明は、特殊毛羽を有する織編物の製造方法
に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a woven or knitted fabric having special fluff.
従来より、織編物の表面に毛羽を与える方法の
1つとして針布起毛があり、他の方法として針布
の代りにエメリークロス等を利用するものがあ
り、用途により使い分けられ、種々の起毛商品を
提供している。 Conventionally, one method of giving fluff to the surface of woven or knitted fabrics is to use cloth raising, and other methods include using emery cloth instead of cloth. is provided.
従来の、このような起毛商品は、いずれも、織
編物を構成する単繊維そのものをループ状に引き
出し、該ループをカツトして起毛繊維とする過程
を経て得られるため、得られる立毛又は毛羽は、
単繊維を基にした太さや長さを有するものであ
る。又、極く最近では前記の立毛、又は毛羽の改
良として、1.0デニール以下の極細繊維を使用す
るものが提案されている。 All of these conventional raised products are obtained by pulling out the single fibers that make up the woven or knitted fabric into a loop and cutting the loops to make raised fibers. ,
It has a thickness and length based on a single fiber. Also, very recently, as an improvement on the above-mentioned napping or fuzz, it has been proposed to use ultrafine fibers of 1.0 denier or less.
しかし乍がら、該極細繊維を用いても、その繊
度や長さには、依然として制限が存在するもので
ある。即ち、該極細繊維は、貼り合せ型の複合繊
維を用いて起毛し、後に、前記貼り合せを分離す
る方法、又は、海島型の複合繊維を用いて起毛
し、後に海成分を溶解除去する方法等により得ら
れるが、紡糸口金や紡糸工程の条件から、無限に
細く、且つ、無段階に繊度を変化せしめて該複合
繊維を紡糸することは不可能なことであり、従つ
て得られる極細繊維も、太さに制限を有し、かか
る太さに制限を有する繊維から得られる立毛、又
は毛羽は、長さにも制限を有することとなるので
ある。 However, even if such ultrafine fibers are used, there are still limitations on their fineness and length. That is, the ultrafine fibers can be raised by using a bonded composite fiber and then separating the bond, or by raising the ultrafine fiber by using a sea-island composite fiber and then dissolving and removing the sea component. However, due to the conditions of the spinneret and the spinning process, it is impossible to spin infinitely fine composite fibers with stepless changes in fineness. However, there is a limit to the thickness, and the napped or fluff obtained from fibers having such a limit to the thickness also has a limit to the length.
本発明の目的は、従来からある長い毛羽ではな
く、肉眼では殆んど判定出来ない程の長さの毛羽
を含む極く短かい毛羽を模様状に配した織編物の
製造法を提案することにある。 The purpose of the present invention is to propose a method for producing a woven or knitted fabric in which extremely short fluffs, including fluffs so long that they are almost undetectable to the naked eye, are arranged in a pattern, instead of the conventional long fluffs. It is in.
即ち、本発明は、非相溶性の添加剤を配合せし
めたポリエステル系繊維からなる織編物に凹凸加
工処理を施し、しかる後に、該織編物の凸部表面
をバツフイング処理し、該バツフイング処理の
前、又は後に、アルカリ溶液で処理することによ
り、該凸部表面にある繊維をミクロフイブリル化
させることを特徴とする特殊毛羽を有する織編物
の製造方法にある。 That is, in the present invention, a woven or knitted fabric made of a polyester fiber blended with an incompatible additive is subjected to an uneven processing treatment, and then the surface of the convex portion of the woven or knitted fabric is subjected to a buffing treatment, and before the buffing treatment, The present invention also provides a method for producing a woven or knitted fabric having special fuzz, characterized in that the fibers on the surface of the convex portion are microfibrillated by treatment with an alkaline solution.
以下、本発明を詳細に説明する。 The present invention will be explained in detail below.
本発明方法により得られる織編物は、ポリエス
テル系繊維からなり、且つ、該ポリエステル繊維
は、ポリエステルとは非相溶性の添加剤を配合せ
しめたものである。ここに非相溶性の添加剤とし
ては、有機化合物だけでなく無機物であつてもよ
いが、ミクロフイブリルを形成させるためには、
一般式R・SO3Mで表わされる有機スルホン酸の
金属塩が好ましく使用される。 The woven or knitted fabric obtained by the method of the present invention is made of polyester fibers, and the polyester fibers are blended with additives that are incompatible with polyester. Incompatible additives may be not only organic compounds but also inorganic substances, but in order to form microfibrils,
Metal salts of organic sulfonic acids represented by the general formula R.SO 3 M are preferably used.
但し、前記一般式において、Rは炭素数3〜30
のアルキル基又は、炭素数7〜40のアリール基、
もしくはアルキルアリール基、Mはアルカリ金
属、若しくはアルカリ土類金属を示す。又、Rが
アルキル基又はアルキルアリール基である時は、
直鎖状あるいは分岐した側鎖を有していてもよ
い。MとしてNa、K、Li等のアルカリ金属、
Mg、Ca等のアルカリ土類金属が挙げられるが、
なかでもNa、Kが好ましい。なお、有機スルホ
ン酸金属塩の使用に際しては、単一の化合物であ
る必要はなく、各種のアルキル基あるいはアルキ
ルアリール基を有する有機スルホン酸金属塩の混
合物であつても良い。このような有機スルホン酸
金属塩としては、具体的には、ステアリルスルホ
ン酸ソーダ、オクチルスルホン酸ソーダ、ドデシ
ルスルホン酸ソーダ、炭素数の平均が14であるア
ルキルスルホン酸ソーダの混合物、ドデシルベン
ゼンスルホン酸ソーダ、オクタデシルベンゼンス
ルホン酸ソーダ、ノニルジフエニルエーテルスル
ホン酸ソーダ等が挙げられる。 However, in the above general formula, R has 3 to 30 carbon atoms.
an alkyl group or an aryl group having 7 to 40 carbon atoms,
or an alkylaryl group, M represents an alkali metal or an alkaline earth metal. Moreover, when R is an alkyl group or an alkylaryl group,
It may have a linear or branched side chain. M is an alkali metal such as Na, K, Li, etc.
Examples include alkaline earth metals such as Mg and Ca,
Among these, Na and K are preferred. Note that when using the organic sulfonic acid metal salt, it is not necessary to use a single compound, and a mixture of organic sulfonic acid metal salts having various alkyl groups or alkylaryl groups may be used. Specifically, such organic sulfonic acid metal salts include sodium stearyl sulfonate, sodium octylsulfonate, sodium dodecyl sulfonate, a mixture of sodium alkyl sulfonates having an average carbon number of 14, and dodecylbenzenesulfonic acid. Examples include soda, sodium octadecylbenzenesulfonate, and sodium nonyldiphenyl ether sulfonate.
本発明方法は、かかる添加剤配合のポリエステ
ル系繊維からなる織編物に、凹凸加工処理を施す
ものである。 In the method of the present invention, a woven or knitted fabric made of polyester fibers containing such additives is subjected to an uneven treatment.
この凹凸加工処理とは、凹凸模様を有する1対
のグラビア・ローラや、凹凸が噛み合う凹凸ロー
ラ等のエンボス加工に使用される手段が有効に用
いられる。 For this uneven processing, means used for embossing, such as a pair of gravure rollers having an uneven pattern or uneven rollers in which the uneven surfaces are engaged, are effectively used.
かくして凹凸を付与された織編物は、バツフイ
ング処理を施される。このバツフイング処理は、
例えば、粒度#240番のサンドペーパーを使用し
て行われる。又、このバツフイングの前、又は後
でアルカリ溶液で処理することが必要であり、こ
のアルカリ溶液による処理は、前記ポリエステル
系繊維の減量率で示せば、5〜35%の範囲で行う
ことがミクロフイブリル化促進のためには好まし
い。 The textured woven or knitted fabric is subjected to a buffing process. This buffing process is
For example, this is done using #240 grit sandpaper. In addition, it is necessary to treat with an alkaline solution before or after this buffing, and the treatment with this alkaline solution can be carried out in a range of 5 to 35% in terms of the weight loss rate of the polyester fiber. Preferable for promoting fibrillation.
又、前記のアルカリ加水分解処理は、アルカリ
ペーストを織編物の凸部表面にコーテイングする
方法により、該凸部表面の繊維に対してのみ行う
ことが出来、その結果、織編物の凸部表面にある
繊維のみをミクロフイブリル化が起り易い状態の
もとにおくことも可能である。 In addition, the alkali hydrolysis treatment described above can be performed only on the fibers on the surface of the convex portion of the woven or knitted material by coating the surface of the convex portion of the woven or knitted material with an alkali paste. It is also possible to subject only certain fibers to conditions where microfibrillation is likely to occur.
以上、述べたように、本発明方法により得られ
る織編物は、凸部表面に特殊な毛羽を有するもの
となり、該凸部を模様状に配置せしめることによ
り、前記特殊毛羽を模様状に配置せしめるもので
ある。 As described above, the woven or knitted fabric obtained by the method of the present invention has special fluff on the surface of the convex portions, and by arranging the convex portions in a pattern, the special fluff is arranged in a pattern. It is something.
又、前記の特殊毛羽は、前記のポリエステル系
繊維をミクロフイブリル化することにより得られ
るものであるが、このミクロフイブリル化された
フイブリルの直径は、その見掛直径で、0.01〜5μ
の範囲内にあり、且つ、該範囲内で無段階に種々
の太さを有するものである。又、該特殊毛羽は、
その長さが1.0mm以下であり、かかる太さと長さ
の毛羽で覆われた凸部表面は、毛羽を有すると云
えども、極めてプレーンで、平滑であり、肉眼で
は判定が困難な毛羽に覆われているのである。 Further, the above-mentioned special fluff is obtained by microfibrillating the above-mentioned polyester fibers, and the apparent diameter of the microfibrillated fibrils is 0.01 to 5μ.
, and has various thicknesses within the range. In addition, the special fluff is
The length of the convex part is 1.0 mm or less and the surface of the convex portion covered with fluff of such thickness and length is extremely plain and smooth even though it has fluff, and is covered with fluff that is difficult to judge with the naked eye. It is being understood.
尚、前記の見掛け直径は、以下のようにして測
定することが出来る。 Incidentally, the above-mentioned apparent diameter can be measured as follows.
見掛け直径
ミクロフイブリル化せしめた毛羽の電子顕微
鏡写真を標準スケールと共に写し、写された毛
羽の直径を読取り顕微鏡で測定し、電子顕微鏡
の拡大倍率と、前記標準スケールとから毛羽の
見掛け直径を求める方法による。Apparent Diameter Take an electron micrograph of microfibrillated fluff along with a standard scale, measure the diameter of the photographed fluff with a reading microscope, and calculate the apparent diameter of the fluff from the magnification of the electron microscope and the standard scale. Depends on the method.
又、本発明方法で得られる特殊毛羽を有する織
編物は、模様状に配された凸部表面だけに、該毛
羽を生起せしめたものであり、毛羽自体、肉眼で
は判定出来ない程度のものが可能であるため、か
かる特殊毛羽によつて、毛羽を有する部分と、毛
羽を有しない部分では織編物の表面の光の反射に
差異が生じ、極めて特異な表面効果を得ることが
出来る。 In addition, the woven or knitted fabric having special fuzz obtained by the method of the present invention has the fuzz only on the surface of the convex portions arranged in a pattern, and the fuzz itself is of such a degree that it cannot be detected with the naked eye. Because of this, the special fluff causes a difference in light reflection on the surface of the woven or knitted fabric between the fluffed part and the non-fuzzed part, making it possible to obtain a very unique surface effect.
以下、実施例により説明する。 Examples will be explained below.
実施例
ジメチルテレフタレート197部、エチレングリ
コール124部及び酢酸カルシウムの0.118部を精留
塔付重縮合用フラスコへ入れ、常法に従つてエス
テル交換反応を行ない、理論量のメタノール留出
後、反応生成物を精留塔付重縮合用フラスコへ移
し、安定剤としてトリメチルホスフエート0.112
部、重縮合触媒として酸化アンチモン0.079部を
加え、温度280℃、常圧で30分反応させ、次いで
30mmHgの減圧下で15分反応させた後、一旦、常
圧にもどし、添加剤として炭素数8〜20で平均炭
素数が14であるアルキルスルホン酸ソーダの混合
物を2部添加した後、系内を除々に減圧し、撹拌
下80分間反応させた。Example 197 parts of dimethyl terephthalate, 124 parts of ethylene glycol, and 0.118 parts of calcium acetate were placed in a polycondensation flask equipped with a rectifying column, and a transesterification reaction was carried out according to a conventional method. After distilling off the theoretical amount of methanol, the reaction product was The material was transferred to a polycondensation flask with a rectification column, and 0.112% of trimethyl phosphate was added as a stabilizer.
1 part, 0.079 part of antimony oxide as a polycondensation catalyst was added, and the reaction was carried out at a temperature of 280°C and normal pressure for 30 minutes, and then
After reacting for 15 minutes under a reduced pressure of 30 mmHg, the pressure was returned to normal, and after adding 2 parts of a mixture of sodium alkyl sulfonates having 8 to 20 carbon atoms and an average carbon number of 14 as an additive, the system was The pressure was gradually reduced, and the mixture was reacted for 80 minutes with stirring.
最終内温280℃、最終内圧0.32mmHgであり、得
られたポリマーの極限粘度は0.65であつた。 The final internal temperature was 280°C, the final internal pressure was 0.32 mmHg, and the obtained polymer had an intrinsic viscosity of 0.65.
反応終了後、該ポリマーを常法に従いチツプ化
し、乾燥し、該乾燥チツプを常法に従い、溶融紡
糸し、得られた未延伸糸を、3.0倍に延伸し、
800m/minの延伸速度で捲取つた。かくして得
られた添加剤配合のポリエステルフイラメント糸
(50デニール/36フイラメント)を用いて、経糸
用にS300T/M、緯糸用にはS、3000T/M、
Z、3000T/Mの撚を与えて、平織(パレス)を
製織した。 After the reaction, the polymer is chipped according to a conventional method, dried, and the dried chips are melt-spun according to a conventional method, and the resulting undrawn yarn is stretched 3.0 times,
It was rolled up at a drawing speed of 800 m/min. Using the polyester filament yarn (50 denier/36 filaments) containing additives obtained in this way, S300T/M for the warp, S, 3000T/M for the weft,
Z, a twist of 3000T/M was applied to weave a plain weave (paris).
該織物を、しぼ立て→乾燥→プレ・セツト→凹
凸加工処理→バツフイング→アルカリ溶液処理→
染色→フアイナル・セツトの各工程に通した。凹
凸加工処理は、温度150℃の状態でエンボスロー
ラで加工し、バツフイングは凸部表面だけに行う
ものである。 The fabric is grained → dried → pre-set → uneven treatment → buffing → alkaline solution treatment →
It went through each step of dyeing → final setting. The unevenness processing is performed using an embossing roller at a temperature of 150°C, and buffing is performed only on the surface of the protrusions.
得られた織物は、該凸部表面だけに特殊毛羽を
有し、この毛羽を電子顕微鏡で観察すると、この
毛羽は繊維がフイブリル化されて得られたもので
あつた。又、この毛羽を有する部分と、毛羽を有
しない部分とでは色相が異なり、毛羽を有する部
分は、毛羽を有しない部分より、見かけ淡染化さ
れ、濃淡の模様を有するものであつた。 The resulting fabric had special fuzz only on the surface of the convex portions, and when this fuzz was observed under an electron microscope, it was found that the fuzz was obtained by fibrillation of the fibers. Further, the hue was different between the part with fluff and the part without fluff, and the part with fluff was apparently lighter dyed and had a pattern of shading than the part without fluff.
Claims (1)
ル系繊維からなる織編物に凹凸加工処理を施し、
しかる後に、該織編物の凸部表面をバツフイング
処理し、該バツフイング処理の前、又は後にアル
カリ溶液で処理することにより、該凸部表面にあ
る繊維をミクロフイブリル化させて、見掛直径
0.01〜5μの範囲内で無段階に種々の太さを有し、
かつ、長さが1.0mm以下の特殊毛羽とし、主とし
て該特殊毛羽により該凸部表面を覆わしめたこと
を特徴とする特殊毛羽を有する織編物の製造方
法。1 A woven or knitted fabric made of polyester fibers mixed with incompatible additives is subjected to an uneven treatment,
Thereafter, the surface of the convex portion of the woven or knitted material is subjected to a buffing treatment, and the fibers on the surface of the convex portion are microfibrillated by being treated with an alkaline solution before or after the buffing treatment, and the apparent diameter is
It has various thicknesses steplessly within the range of 0.01 to 5μ,
A method for producing a woven or knitted article having special fluff, characterized in that the special fluff has a length of 1.0 mm or less, and the surface of the convex portion is mainly covered with the special fluff.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19372281A JPS5898474A (en) | 1981-12-03 | 1981-12-03 | Production of knitted fabric having special feather |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19372281A JPS5898474A (en) | 1981-12-03 | 1981-12-03 | Production of knitted fabric having special feather |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5898474A JPS5898474A (en) | 1983-06-11 |
| JPS636671B2 true JPS636671B2 (en) | 1988-02-10 |
Family
ID=16312701
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19372281A Granted JPS5898474A (en) | 1981-12-03 | 1981-12-03 | Production of knitted fabric having special feather |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5898474A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2611334B2 (en) * | 1988-05-25 | 1997-05-21 | 東洋紡績株式会社 | Processing method of regenerated cellulose fiber woven / knitted fabric |
-
1981
- 1981-12-03 JP JP19372281A patent/JPS5898474A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5898474A (en) | 1983-06-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS581221B2 (en) | Shikagawa henshiyokubutsuno | |
| DE60034449T2 (en) | FLAME DELAYING POLYESTER FIBERS, FABRICS, KNITWEAR, NONWOVENS AND SUEDE WOVEN OR KNITTED TEXTILE PRODUCTS FROM THESE FIBERS | |
| JPS638222B2 (en) | ||
| EP0073437B1 (en) | Dyed polyester fiber composite structure | |
| JPS636671B2 (en) | ||
| JPH0258374B2 (en) | ||
| JPS6356346B2 (en) | ||
| JP2019183366A (en) | Fabric, manufacturing method thereof, and textile product | |
| JP3863051B2 (en) | Polyester spotted yarn | |
| JPS6131233B2 (en) | ||
| JPH0633319A (en) | Hollow conjugate yarn and its production | |
| JPS6131232B2 (en) | ||
| JP2726201B2 (en) | Method for producing clear polyester fiber for strong twist | |
| JP3856620B2 (en) | Spanish fabric | |
| KR0141853B1 (en) | Manufacturing method of deep color polyester yarn | |
| JP3333831B2 (en) | Polyester thick yarn | |
| EP0056907A1 (en) | Process for the preparation of suède-like raised fabrics | |
| JP3157643B2 (en) | Method for producing fiber, yarn or fabric | |
| JPH02175965A (en) | Production of porous polyamide fiber | |
| JPH0151589B2 (en) | ||
| GB1601586A (en) | Process for the production of copolyesters | |
| JPS59116466A (en) | Treatment of polyester fiber | |
| JPS643982B2 (en) | ||
| JP2004156172A (en) | Easily fibrillating polyester yarn | |
| JPS62141120A (en) | Polyester conjugated yarn |