JPH01239167A - Crimped twist yarn knitted fabric - Google Patents
Crimped twist yarn knitted fabricInfo
- Publication number
- JPH01239167A JPH01239167A JP63056321A JP5632188A JPH01239167A JP H01239167 A JPH01239167 A JP H01239167A JP 63056321 A JP63056321 A JP 63056321A JP 5632188 A JP5632188 A JP 5632188A JP H01239167 A JPH01239167 A JP H01239167A
- Authority
- JP
- Japan
- Prior art keywords
- yarn
- knitted fabric
- reactive compound
- fibrillation
- cloth
- 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
- 239000004744 fabric Substances 0.000 title claims abstract description 36
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- 125000002091 cationic group Chemical group 0.000 claims abstract description 11
- 229920003043 Cellulose fiber Polymers 0.000 claims abstract description 10
- 239000004627 regenerated cellulose Substances 0.000 claims abstract description 9
- 229920002678 cellulose Polymers 0.000 claims abstract description 6
- 239000001913 cellulose Substances 0.000 claims abstract description 6
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 5
- 206010061592 cardiac fibrillation Diseases 0.000 abstract description 13
- 230000002600 fibrillogenic effect Effects 0.000 abstract description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 12
- 125000000217 alkyl group Chemical group 0.000 abstract description 5
- 229910052736 halogen Inorganic materials 0.000 abstract description 4
- 125000005843 halogen group Chemical group 0.000 abstract description 3
- 150000002367 halogens Chemical class 0.000 abstract description 3
- LTVDFSLWFKLJDQ-UHFFFAOYSA-N α-tocopherolquinone Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)(O)CCC1=C(C)C(=O)C(C)=C(C)C1=O LTVDFSLWFKLJDQ-UHFFFAOYSA-N 0.000 abstract description 3
- 125000003118 aryl group Chemical group 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229920000297 Rayon Polymers 0.000 description 6
- 238000004043 dyeing Methods 0.000 description 5
- 239000002964 rayon Substances 0.000 description 5
- QKSIFUGZHOUETI-UHFFFAOYSA-N copper;azane Chemical compound N.N.N.N.[Cu+2] QKSIFUGZHOUETI-UHFFFAOYSA-N 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 4
- WHDHZGMNEDEKTC-UHFFFAOYSA-N 1-chloro-3-(dimethylamino)propan-2-ol;hydrochloride Chemical compound [Cl-].C[NH+](C)CC(O)CCl WHDHZGMNEDEKTC-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- -1 etc. Polymers 0.000 description 3
- 238000009981 jet dyeing Methods 0.000 description 3
- 238000006748 scratching Methods 0.000 description 3
- 230000002393 scratching effect Effects 0.000 description 3
- WUMJCTFQUXKJOM-UHFFFAOYSA-N 3-hydroxypropyl(dimethyl)azanium;chloride Chemical compound Cl.CN(C)CCCO WUMJCTFQUXKJOM-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920001407 Modal (textile) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- MWOAZBKCGLQRPF-UHFFFAOYSA-N [Cl-].O1C(C[NH+](CC)CC)C1 Chemical compound [Cl-].O1C(C[NH+](CC)CC)C1 MWOAZBKCGLQRPF-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- AVKLPTSKTBCMGS-UHFFFAOYSA-N but-2-ene-1,2,3,4-tetrol urea Chemical compound NC(=O)N.C(O)C(=C(O)CO)O AVKLPTSKTBCMGS-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- KDJDBBUMQVLTGP-UHFFFAOYSA-N dimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1CO1 KDJDBBUMQVLTGP-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- YQFOHQBSENCNTR-UHFFFAOYSA-M oxiran-2-ylmethyl(tripropyl)azanium;chloride Chemical compound [Cl-].CCC[N+](CCC)(CCC)CC1CO1 YQFOHQBSENCNTR-UHFFFAOYSA-M 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- HFIYIRIMGZMCPC-YOLJWEMLSA-J remazole black-GR Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(\N=N\C=3C=CC(=CC=3)S(=O)(=O)CCOS([O-])(=O)=O)C(O)=C2C(N)=C1\N=N\C1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 HFIYIRIMGZMCPC-YOLJWEMLSA-J 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 230000005068 transpiration Effects 0.000 description 1
- JMMAMAWBEJRFQN-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;bromide Chemical compound [Br-].C[N+](C)(C)CC1CO1 JMMAMAWBEJRFQN-UHFFFAOYSA-M 0.000 description 1
- AISMNBXOJRHCIA-UHFFFAOYSA-N trimethylazanium;bromide Chemical compound Br.CN(C)C AISMNBXOJRHCIA-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Woven Fabrics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はしぼ立ち撚糸編織物に関する。更に詳しくは耐
フィブリル化の改善されたしぼ立ち編織物に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a grained twisted yarn knitted fabric. More specifically, the present invention relates to a grained knitted fabric with improved fibrillation resistance.
従来、再生セルロース繊維のしぼ立ち撚糸編織物におい
て、織物では(蒸散500 T / m以上の糸条を経
糸又は争糸に用い、又、編物では撚数100T/m以上
の糸条を用いた上で、これらの製品の特徴であるしぼを
出すため、染色加工々程でしぼ立て処理を行なう。該工
程及び染色、仕上等のウェット状態にて、布帛同志ある
いは布帛と染色加工機械との摩擦により布帛表面が部分
的にこすれ、フィブリル化を起こし、その部分が他の部
分に比べて、光沢、色相等が変化し、品位の低いものと
なる。(以下、この光沢、色相等の変化を「スレ」と称
す。)
「スレ」の防止方決としては、これまで次の2つノ方法
カ採用されていた。■原糸製造段階にて油剤等を付与し
て、原糸に柔軟性を与えて、摩擦係数を少なくして「ス
レ」発生を防止する方法。Conventionally, in knitted fabrics made of regenerated cellulose fibers with grained twist, yarns with a transpiration rate of 500 T/m or more are used as warp or warp yarns, and knitted fabrics with yarns with a twist rate of 100 T/m or more are used. In order to bring out the grain that is a characteristic of these products, a graining process is performed during the dyeing process.During this process, dyeing, and finishing in the wet state, friction between the fabrics or between the fabric and the dyeing machine causes The surface of the fabric is partially rubbed, causing fibrillation, and the gloss, hue, etc. of that area changes compared to other areas, resulting in lower quality. (Hereinafter, this change in gloss, hue, etc. will be referred to as " The following two methods have been adopted so far to prevent "scratching".■ Adding oil, etc. to the yarn at the yarn manufacturing stage to make the yarn flexible. A method of reducing the coefficient of friction and preventing the occurrence of "scratches".
■布帛の染色加工時に浴中に柔軟剤等を加えて布帛の摩
擦係数を少なくして「スレ」発生を防止する方法。■A method of adding softeners, etc. to the bath during the dyeing process of fabrics to reduce the coefficient of friction of the fabrics and prevent the occurrence of "scratches".
上記の方法は何れも「スレ」発生防止には殆んど効果が
なく、フィブリル化の改善はなされていない。All of the above methods have little effect on preventing the occurrence of "scratches" and do not improve fibrillation.
本発明者らは、上記の問題について研究した結果、単に
原糸の摩擦係数を少なくするだけでは、フィブリル化防
止には効果がなく、「スレ」が発生する事が判り、又、
フィブリル化防止として、ジメチロール・ジヒドロキシ
エチレン尿素等による樹脂加工は繊維の強度低下が大き
く、「スレ」が目立つ事が判かった。As a result of research into the above-mentioned problem, the present inventors found that simply reducing the coefficient of friction of the yarn is not effective in preventing fibrillation and causes "scratching".
It was found that resin treatment with dimethylol, dihydroxyethylene urea, etc. to prevent fibrillation caused a significant decrease in the strength of the fibers, resulting in noticeable "fraying".
本発明は、しぼ立ち撚糸編織物の特性を損なわずに、耐
フィブリル化を改善して、「スレ」発生を防止する事を
目的とする。The object of the present invention is to improve the fibril resistance and prevent the occurrence of "fraying" without impairing the characteristics of grained twisted yarn knitted fabrics.
上記の目的を達成すべく、鋭意研究の結果、再生セルロ
ース繊維のフィブリル化を防止し、かつ該繊維に耐久性
に優れた柔軟性を付与する事により、「スレ」が改善さ
れる事を見出し、本発明を完成するに至った。In order to achieve the above objective, as a result of intensive research, it was discovered that "scratching" could be improved by preventing fibrillation of regenerated cellulose fibers and imparting flexibility with excellent durability to the fibers. , we have completed the present invention.
本発明の目的は糸又は布帛状態でカチオン性反応性化合
物とセルロースとの反応物が形成されている事が特徴と
される再生セルロース繊維のしぼ立ち1熱系編織物によ
って達成される。The object of the present invention is achieved by a wrinkled single-thermal knitted fabric made of regenerated cellulose fibers, which is characterized in that a reaction product of a cationic reactive compound and cellulose is formed in the form of yarn or fabric.
以下、本発明について、更に詳しく述べる。The present invention will be described in more detail below.
本発明におけるカチオン性の反応性化合物とは、再生セ
ルロース繊維と反応性を有するもので、その−例を示す
と、一般式(1)〜(III)に示すものが挙げられる
。The cationic reactive compound in the present invention is one that has reactivity with regenerated cellulose fibers, and examples thereof include those shown in general formulas (1) to (III).
0式中、R,、R,及びR3は水素又は炭素数1〜4個
のアルキル基であり、XIはハロゲンである。〕
0式中、Rn、Rs及びRb1J水素又は炭素数1〜4
個のアルキル基、アリール基であり、x2及びxゴはハ
ロゲンである。〕
二1uしμ【L
〔式中、A+ 、Az 、A3及びA4は夫々水素、炭
素数1〜18のアルキル基、シクロアルキル基、了り−
ル基又は炭素数7〜18のアラルキル基であり、B1及
びB2は共に水素の場合を除く、夫々が水素、−011
□・CIl・CIl□X(Xはハロゲン原子)、il
!
(Xはハロゲン原子)、Yは残酸基である。又、nは2
以上の整数であり、Xは1以上の整数である。〕
一般式(I)に示される具体的な化合物として、例えば
、グリシジル・トリメチルアンモニウムクロライド、グ
リシジル・トリプロピルアンモニウムクロライド、グリ
シジル・トリメチルアンモニウムプロミドなどが挙げら
れる。In formula 0, R, , R, and R3 are hydrogen or an alkyl group having 1 to 4 carbon atoms, and XI is a halogen. ] In formula 0, Rn, Rs and Rb1J hydrogen or carbon number 1-4
are an alkyl group or an aryl group, and x2 and x are halogens. [In the formula, A+, Az, A3 and A4 are each hydrogen, an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group,
B1 and B2 are each hydrogen, -011
□・CIl・CIl□X (X is a halogen atom), il! (X is a halogen atom), Y is a residual acid group. Also, n is 2
is an integer of 1 or more, and X is an integer of 1 or more. ] Specific examples of the compounds represented by the general formula (I) include glycidyl trimethylammonium chloride, glycidyl tripropylammonium chloride, glycidyl trimethylammonium bromide, and the like.
又、−i式(II)に示される具体的な化合物として、
例えば、3−クロロ−2−ヒドロキシ・プロピルトリメ
チルアンモニウムクロライド、3−ブロム−2−ヒドロ
キシ・プロピルトリエチレンアンモニウムクロライドな
とが挙げられる。Moreover, as a specific compound represented by formula (II),
Examples include 3-chloro-2-hydroxypropyltrimethylammonium chloride and 3-bromo-2-hydroxypropyltriethyleneammonium chloride.
又、一般式(III)に示される具体的な化合物として
トリメチレンビス(3−クロロ−2−ヒトI:]キシプ
ロピル−ジメチルアンモニウムクロライド)、ヘキサメ
チレンビス(3−クロロ−2−ヒドロキシプロピル・ジ
メチルアンモニウムクロライド)、トリメチレンビス(
グリシジル・ジメチルアンモニウムクロライド)、トリ
メチレンビス(グリシジル・ジエチルアンモニウムクロ
ライド)などが挙げられる。Further, as specific compounds represented by the general formula (III), trimethylenebis(3-chloro-2-human I:]xypropyl-dimethylammonium chloride), hexamethylenebis(3-chloro-2-hydroxypropyl dimethyl ammonium chloride), trimethylene bis(
Glycidyl dimethyl ammonium chloride), trimethylenebis (glycidyl diethylammonium chloride), etc.
本発明における再生セルロース繊維とは、ビスコース法
レーヨン、銅アンモニア法レーヨン、ポリノジックなど
と、及び合成繊維との混紡、lYコ繊、交編、交織され
たものである。The regenerated cellulose fibers in the present invention are those obtained by blending, lY co-fiber, inter-knitting, and inter-weaving with viscose rayon, cuprammonium rayon, polynosic, etc., and synthetic fibers.
本発明において、糸又は布帛状態でカチオン性の反応性
化合物で処理するとは、再生セルロース繊維の糸あるい
は編物、織物に対して、物理的あるいは化学的に付与し
、該反応性化合物とセルロースとの反応物が形成される
事である。その付与方法は、浸漬法、パ・7ド法、印捺
法、スプレー法等であり、反応において必要な酸、アル
カリ、各種触媒を使用しても良い。特にアルカリ剤の使
用が好ましく、水酸化ナトリウム、炭酸ナトリウム、炭
酸水素ナトリウムなどが好ましい。In the present invention, treating the yarn or fabric with a cationic reactive compound means to physically or chemically apply it to the yarn, knitted fabric, or woven fabric of regenerated cellulose fibers, so that the reactive compound and cellulose are treated with a cationic reactive compound. The formation of reactants. The method for applying it is a dipping method, a padding method, a printing method, a spraying method, etc., and acids, alkalis, and various catalysts necessary for the reaction may be used. In particular, it is preferable to use an alkaline agent, and sodium hydroxide, sodium carbonate, sodium hydrogen carbonate, etc. are preferable.
又、反応は浴中、乾熱、温熱などがあり、反応温度は、
浸漬法では0−150℃であり、他の方法では0〜20
0°Cである。又、反応時間は処理温度や処理方法によ
り適宜決定される。In addition, the reaction can be carried out in a bath, dry heat, warm heat, etc., and the reaction temperature is
In the immersion method, the temperature is 0-150℃, and in other methods, the temperature is 0-20℃.
It is 0°C. Further, the reaction time is appropriately determined depending on the treatment temperature and treatment method.
次にカチオン性の反応性化合物の使用量は1〜200g
/Lであり、好ましくはio〜150g/L以上である
。1 g/Lでは耐久性に乏しく、200g/L以上で
は、再生セルロース繊維の物性低下をきたすので好まし
くない。Next, the amount of cationic reactive compound used is 1 to 200 g.
/L, preferably io to 150 g/L or more. If it is 1 g/L, the durability is poor, and if it is more than 200 g/L, the physical properties of the regenerated cellulose fibers will deteriorate, which is not preferable.
なお、前記方法により供試されたカチオン性反応性化合
物とセルロースとの反応物は、次の全窒素量の測定法に
より確認できる。Note that the reaction product between the cationic reactive compound and cellulose tested by the above method can be confirmed by the following method for measuring the total nitrogen amount.
微量全窒素分析装置TN−10C三菱化成0菊製)にて
全窒素量を測定する。全窒素量11000pp/ g
繊維以上が確認できる。The total nitrogen amount is measured using a trace total nitrogen analyzer TN-10C (manufactured by Mitsubishi Kasei Ogiku). Total nitrogen amount 11000pp/g
More than fibers can be confirmed.
以下、実施例を以って本発明を更に詳しく説明する。 Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施■土
銅アンモニア法レーヨン糸75d/45f (旭化成
工業■〕ヲトリメチレンビス(3−クロロ−2−ヒドロ
キシプロピル・ジメチルアンモニウムクロライド)90
g/L、水酸化ナトリウム13g/Lを含む水溶液にて
、浴比t:zo、8o°Cで30分間処理し、続いて、
酢酸にて中和、水洗、乾燥した。Implementation■ Clay copper ammonia method rayon thread 75d/45f (Asahi Kasei Corporation■) Wotrimethylenebis(3-chloro-2-hydroxypropyl dimethylammonium chloride) 90
g/L and an aqueous solution containing 13 g/L of sodium hydroxide at a bath ratio of t:zo for 30 minutes at 8o°C, followed by
Neutralized with acetic acid, washed with water, and dried.
次にこの糸を撚数120T/mにて撚糸した上で、天竺
績で編成した。Next, this yarn was twisted at a twist rate of 120 T/m, and then knitted using a jersey stitch.
止較拠上
銅アンモニア法レーヨン糸75d /45 f ヲ撚B
120T/mにて撚し、続いて天竺績した。Copper ammonia method rayon yarn 75d/45f twisted B
It was twisted at 120T/m, and then rolled up.
上述の方法により得られた実施例1と比較例1の編物を
液流染色機にてCI Reactive Black
55%owfで黒色に染色して得られた各種編物の性能
を第1表に示す。The knitted fabrics of Example 1 and Comparative Example 1 obtained by the above method were dyed with CI Reactive Black using a jet dyeing machine.
Table 1 shows the performance of various knitted fabrics obtained by dyeing black at 55% owf.
第 1 表 (注)「スレ」の状態 ○ 布帛11当りにスレが全くない。Table 1 (Note) “Thread” condition ○ There are no scratches on fabric 11.
△ 布帛IM当りにスレが10か所未満である。△ There are less than 10 scratches per fabric IM.
× 布帛1−当りにスレが10か所以上である。× There are 10 or more scratches per fabric.
「フィブリル化」の状態 ○ フィブリル化なし。“Fibrillation” state ○ No fibrillation.
八 単糸が一部切断されている。8. Some of the single threads are cut.
× 単糸が切断され毛羽立ちがある。× Single threads are cut and fluffy.
第1表より、本発明の編物は、「ス゛し」及びフィブリ
ル化の発生がなく、柔軟な風合である。As shown in Table 1, the knitted fabric of the present invention does not cause "sweeping" or fibrillation, and has a soft texture.
去施拠主
銅アンモニア法レーヨン織物(75/75デシン・・・
経糸の撚数800 T / m )をトリメチレンビス
(3−クロロ−2−ヒドロキシプロピル・ジメチルアン
モニウムクロライド)100g/L、水酸化ナトリウム
13g/Lを含む水溶液に浸漬し、絞液後、巻取り、ポ
リエチレンフィルムにて密封し、20℃にて20時間反
応させ、続いて、酢酸にて中和、水洗、乾燥した。Copper ammonia method rayon fabric (75/75 decinene...
A warp yarn (twist number 800 T/m) was immersed in an aqueous solution containing 100 g/L of trimethylene bis(3-chloro-2-hydroxypropyl dimethylammonium chloride) and 13 g/L of sodium hydroxide, and after squeezing the liquid, it was wound up. The mixture was sealed with a polyethylene film and reacted at 20° C. for 20 hours, followed by neutralization with acetic acid, washing with water, and drying.
次にこの織物を液流染色機にてC1,Reactive
Black55%owfで染色した。Next, this fabric is dyed with C1, Reactive using a jet dyeing machine.
It was stained with Black 55% owf.
尖旌炎工
実施例2め織物をトリメチレンビス(3−クロロー2−
ヒドロキシプロピル・ジメチルアンモニウムクロライド
)の代わりにクリシジル・トリメチルアンモニウムプロ
ミドを用いた他は実施例2と同様の条件にて処理した。Trimethylene bis(3-chloro2-
The treatment was carried out under the same conditions as in Example 2, except that chrycidyl trimethyl ammonium bromide was used instead of hydroxypropyl dimethyl ammonium chloride.
尖衡貫」
実施例2の織物をトリメチレンビス(3−クロロ−2−
ヒドロキシプロピル・ジメチルアンモニウムクロライド
)の代わりに3−クロロ−2−ヒドロキシ・プロピルト
リメチルアンモニウムクロライドを用いた他は実施例2
と同様の条件にて処理した。The fabric of Example 2 was treated with trimethylene bis(3-chloro-2-
Example 2 except that 3-chloro-2-hydroxypropyltrimethylammonium chloride was used instead of hydroxypropyldimethylammonium chloride)
It was treated under the same conditions.
ル較尉叉
銅アンモニア法レーヨン織物(75/75デシン〕を液
流染色機にてC1,Reactive Black 5
5%owfで染色した。Copper ammonia method rayon fabric (75/75 decinene) was dyed using a liquid jet dyeing machine.C1, Reactive Black 5
It was stained with 5% owf.
上記の方法により得られた実施例2〜4および比較例2
の性能を第2表に示す。Examples 2 to 4 and Comparative Example 2 obtained by the above method
The performance is shown in Table 2.
以下余白
第 2 表
第2表より、本発明の織物は、何れのものも「スレ」及
びフィブリル化の発生がなく、柔軟な風合である。As shown in Table 2, all of the fabrics of the present invention have a soft texture without any "fraying" or fibrillation.
本発明の編織物では、しぼ立ち撚糸編織物の特性を損な
わずに、耐フィブリル化を改善して、「スレ」発生が防
止される。The knitted fabric of the present invention improves fibrillation resistance and prevents the occurrence of "fraying" without impairing the characteristics of the grained twisted yarn knitted fabric.
Claims (1)
カチオン性反応性化合物とセルロースとの反応物が形成
されている事を特徴とする再生セルロース繊維のしぼ立
ち撚糸編織物。treated with a cationic reactive compound in yarn or fabric form,
A grained twisted yarn knitted fabric made of regenerated cellulose fiber, characterized in that a reaction product between a cationic reactive compound and cellulose is formed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63056321A JPH01239167A (en) | 1988-03-11 | 1988-03-11 | Crimped twist yarn knitted fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63056321A JPH01239167A (en) | 1988-03-11 | 1988-03-11 | Crimped twist yarn knitted fabric |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01239167A true JPH01239167A (en) | 1989-09-25 |
Family
ID=13023906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63056321A Pending JPH01239167A (en) | 1988-03-11 | 1988-03-11 | Crimped twist yarn knitted fabric |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01239167A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995000697A1 (en) * | 1993-06-24 | 1995-01-05 | Courtaulds Fibres (Holdings) Limited | Fabric treatment |
JPH0813336A (en) * | 1994-06-28 | 1996-01-16 | Nobutaka Ono | Method for preventing purified cellulose from being fibrillated |
US5562739A (en) * | 1994-06-01 | 1996-10-08 | Courtaulds Fibres (Holdings) Limited | Lyocell fiber treatment method |
-
1988
- 1988-03-11 JP JP63056321A patent/JPH01239167A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995000697A1 (en) * | 1993-06-24 | 1995-01-05 | Courtaulds Fibres (Holdings) Limited | Fabric treatment |
US5562739A (en) * | 1994-06-01 | 1996-10-08 | Courtaulds Fibres (Holdings) Limited | Lyocell fiber treatment method |
JPH0813336A (en) * | 1994-06-28 | 1996-01-16 | Nobutaka Ono | Method for preventing purified cellulose from being fibrillated |
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