JPH0457909A - Production of anti-pilling acrylic fiber - Google Patents
Production of anti-pilling acrylic fiberInfo
- Publication number
- JPH0457909A JPH0457909A JP16219590A JP16219590A JPH0457909A JP H0457909 A JPH0457909 A JP H0457909A JP 16219590 A JP16219590 A JP 16219590A JP 16219590 A JP16219590 A JP 16219590A JP H0457909 A JPH0457909 A JP H0457909A
- Authority
- JP
- Japan
- Prior art keywords
- spinning
- pilling
- fiber
- less
- acrylic 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.)
- Granted
Links
- 229920002972 Acrylic fiber Polymers 0.000 title claims description 10
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 238000009987 spinning Methods 0.000 claims description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 230000015271 coagulation Effects 0.000 claims description 9
- 238000005345 coagulation Methods 0.000 claims description 9
- 230000008961 swelling Effects 0.000 claims description 6
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 5
- 229920002239 polyacrylonitrile Polymers 0.000 claims description 4
- 239000000835 fiber Substances 0.000 description 22
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000006187 pill Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000011550 stock solution Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 210000004209 hair Anatomy 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 2
- SZHIIIPPJJXYRY-UHFFFAOYSA-M sodium;2-methylprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)CS([O-])(=O)=O SZHIIIPPJJXYRY-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000002166 wet spinning Methods 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 208000005156 Dehydration Diseases 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000008360 acrylonitriles Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は優れた杭ピル性を有するアクリル繊維の製造法
に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for producing acrylic fibers having excellent pile properties.
アクリル1m!纏は他の合成*維に比べ最本羊毛に類似
した柔軟な風合、嵩高性並びに優れた染色性を有し、衣
料用またはインテリア用〈利用されている。しかしなが
らアクリル繊維の編織物は着用中にその表面に毛羽、短
毛等の絡まりあったピリングと呼ばれる毛玉を発生し、
衣料の外観を普しく損い商品価値を低下させるという実
用上の欠点がある。Acrylic 1m! Compared to other synthetic fibers, it has a soft texture similar to that of pure wool, is bulky, and has excellent dyeability, and is used for clothing and interior decoration. However, when knitted fabrics made of acrylic fibers are worn, pilling, which is a tangle of fuzz, short hair, etc., occurs on the surface.
This has the practical drawback of spoiling the appearance of clothing and lowering its commercial value.
かかる状況を背景としてピリングの発生を防止するため
にこれ迄に多くの提案がなされている。例えば特開昭5
9−116409号公報には、繊維の断面形状を真円化
し特定の熱処理条件下で杭ピル性を向上させる方法が開
示されており、又特開昭59−192717号公報には
繊維の引張り強度、結節強伸度を特定の範囲に訃さえる
ことによって抗ピル性を向上させる方法が開示されてい
るが、いずれ本高度化する製品の要求水準を満たすKu
不十分である。Against this background, many proposals have been made to prevent the occurrence of pilling. For example, JP-A-5
9-116409 discloses a method of rounding the cross-sectional shape of fibers to improve pile pilling properties under specific heat treatment conditions, and JP-A-59-192717 discloses a method for improving the tensile strength of fibers. , a method of improving pill resistance by controlling the knot strength and elongation within a specific range has been disclosed, but Ku
Not enough.
本発明け、衣料用等に適する優れた杭ピル性を本つアク
リル*、iaiを提供することにある。The object of the present invention is to provide acrylic*, iai, which has excellent pile-pilling properties and is suitable for clothing and the like.
本発明の要旨とするところは、アクリロニトリルが90
参以上のアクリロニトリル系重合体を224以下含有す
る紡糸原液を紡糸ドラフト17〜1.4で凝固浴に湿式
紡糸し、膨潤炭160〜2504で繊維化して強度sa
p/d以上、結節強度(t/d)と結節伸度(4)の積
が20以下の抗ピル性アクリル繊維を製造することにあ
り、好しくは紡糸原液が3唾以下の水を含有するととに
ある。The gist of the present invention is that acrylonitrile is
A spinning dope containing an acrylonitrile polymer of 224 or more is wet-spun in a coagulation bath at a spinning draft of 17 to 1.4, and is made into fibers with swelling charcoal of 160 to 2504 to obtain a strength of sa.
The objective is to produce anti-pill acrylic fibers with p/d or more and a product of knot strength (t/d) and knot elongation (4) of 20 or less, and preferably the spinning stock solution contains 3 or less water. Then there it is.
以下に本発明を具体的に説明する。The present invention will be specifically explained below.
本発明に用いられるアクリロニトリル系重合体は、90
4以上のアクリロニトリルを含有することが必要である
。アクリロニトリルの含有率がこれよシ少ない場合は衣
料用繊維として必要な繊維物性を損なうので好ましくな
い。又共重合可能な七ツマ−としては、アクリル酸メチ
ル、メタクリル酸メチル等の(メタ)アクリル蒙エステ
ル類、酢酸ビニル、スチレン、アクリル駿アミド類が挙
げられる。又染色性改良のためにrメタ)アクリル酸、
メタアリルスルホン酸ヤビニルベンゼンスルホン酸とそ
れらの種類等の親水性モノマーを共重合させることが挙
げられるが、これらに限定されるものではない。The acrylonitrile polymer used in the present invention has a 90%
It is necessary to contain 4 or more acrylonitriles. If the content of acrylonitrile is less than this, it is not preferable because the physical properties of the fiber required as a clothing fiber will be impaired. Examples of copolymerizable heptamers include (meth)acrylic acid esters such as methyl acrylate and methyl methacrylate, vinyl acetate, styrene, and acrylamide. In addition, r-meth)acrylic acid to improve dyeing properties.
Examples include, but are not limited to, copolymerizing hydrophilic monomers such as methalylsulfonic acid and yavinylbenzenesulfonic acid.
これらの1合体を湿式紡糸する溶剤としては、ジメチル
アセトアミド、ジメチルホルムアミド、ジメチルスルホ
キシド等の有機溶剤、硝酸、ロダン酸ソーダ、塩化亜鉛
等の無S塩の溶剤が挙げられるが、好ましくはジメチル
アセトアミド、ジメチルホルムアミド、ジメチルスルホ
キシド等の有機溶剤が望ましい。これは硝酸、ロダン酸
ソーダ、塩化亜鉛等の無機塩の溶剤では、凝固速度が緩
慢なため目的とする繊維を得難いためである。Examples of the solvent for wet-spinning these monomers include organic solvents such as dimethylacetamide, dimethylformamide, and dimethylsulfoxide, and S salt-free solvents such as nitric acid, sodium rhodanate, and zinc chloride, but dimethylacetamide, Organic solvents such as dimethylformamide and dimethyl sulfoxide are preferred. This is because with inorganic salt solvents such as nitric acid, sodium rhodanate, and zinc chloride, the coagulation rate is slow, making it difficult to obtain the desired fibers.
紡糸原液の重合体濃度は224以下が好ましく、より好
しくは20参以下である。これは通常の紡糸原液濃度よ
り低濃度偶の範囲であり後記する洗浄・延伸糸膨潤度及
び繊維物性を得る為の必須条件の一つである。The polymer concentration of the spinning dope is preferably 224 or less, more preferably 20 or less. This concentration is in a lower concentration range than the usual spinning stock solution concentration, and is one of the essential conditions for obtaining the washing/drawing yarn swelling degree and fiber physical properties described later.
又、紡糸原液に水を添加することKよって凝固条件との
関連はあるが、−維の断面形状がソラ豆型から丸型へと
成形され易くな妙且つ繊維光沢本向上すると込う効果が
得られると共に紡績工程の通過性改善(毛羽、糸切れ減
少)、製品風合の向上が認められる。紡糸原液中に含有
させる水分量は34以下が好ましく、より好ましくは2
4以下である。紡糸原液中の水分が3鴫を継えると原液
のゲル化を意起し紡糸不能となるので望ましくない。Additionally, although it is related to the coagulation conditions, adding water to the spinning dope has the effect of making the cross-sectional shape of the fiber easier to shape from a bean shape to a round shape and improving the fiber luster. At the same time, improvements in passability during the spinning process (reduction in fuzz and thread breakage) and improvement in product texture were observed. The amount of water contained in the spinning dope is preferably 34 or less, more preferably 2
4 or less. If the water content in the spinning solution exceeds 30%, it is not desirable because the solution will gel, making spinning impossible.
次に紡糸条件であるが、この中で特に紡糸ドラフトが重
要である。アクリロニトリル系重合体を湿式紡糸する場
合に紡糸ドラフトや凝固浴組成で繊維構造が規制されて
いくことは公知であるが、本発明において前述の溶剤〜
水系の凝固浴を用いた場合、紡糸ドラフトを17〜1.
4よシ好ましくは19〜1.2 &Cすることが望まし
い。紡糸ドラフトを17未満とすると凝固浴中で糸条が
漂い紡糸性を損なうだけでなく目的とする#l繊維能が
得られず、1.4を超すと糸切れが多発し操業性を著し
く悪化させる。本発明における紡糸ドラフトは、通常よ
り高めの設定としており後記する延伸倍率との関連から
優れた杭ピル性が得られるのである。これは、凝固糸が
形成される過稈において、繊維微細構造がより°高い紡
糸ドラフト(高張力)の作用忙よって適度に破壊され目
的とする抗ピル性に合致したレベルとなったものと考え
られる。Next, there are spinning conditions, and among these, the spinning draft is particularly important. It is known that when wet spinning acrylonitrile polymers, the fiber structure is regulated by the spinning draft and coagulation bath composition.
When using an aqueous coagulation bath, the spinning draft is set at 17 to 1.
4, preferably 19 to 1.2&C. If the spinning draft is less than 17, yarns will drift in the coagulation bath, impairing spinnability, and the desired #l fiber performance will not be obtained; if it exceeds 1.4, yarn breakage will occur frequently and operability will deteriorate significantly. let The spinning draft in the present invention is set higher than usual, and excellent pile pilling properties can be obtained in relation to the stretching ratio described later. This is thought to be due to the fact that in the overculm where coagulated threads are formed, the fiber microstructure is moderately destroyed by the action of the higher spinning draft (high tension) and has reached a level that meets the desired anti-pilling property. It will be done.
凝固浴の組成は、溶剤成分が30〜504より好ましく
は30〜404、水の成分が70〜504より好ましく
は70〜604である。凝固浴の温度は30〜60℃よ
シ好ましくは40〜50℃である。The composition of the coagulation bath is such that the solvent component is more preferably 30 to 404, and the water component is more preferably 70 to 604. The temperature of the coagulation bath is 30-60°C, preferably 40-50°C.
かくして得られた凝固糸を熱水中で洗浄しながら1.5
〜6倍に延伸する。ここで延伸倍率は1.5〜6倍よシ
好ましくF13〜6倍である。While washing the thus obtained coagulated thread in hot water,
Stretch ~6 times. Here, the stretching ratio is 1.5 to 6 times, preferably F13 to 6 times.
かくして得られた凝固糸に含有する溶剤の洗浄処理と延
伸処理を施した糸条の膨潤炭は160〜2504の範囲
にあることが必要であシ、より好ましくは200〜22
04の範囲である。The swollen charcoal of the thread obtained by washing the solvent contained in the coagulated thread thus obtained and drawing it must be in the range of 160 to 2504, more preferably 200 to 22.
The range is 04.
得られた延伸糸を常法により油剤処理、乾燥緩和処理等
を施してアクリル繊維とする。アクリル繊維の抗ピル性
を評価するのに結節強度と結節伸度との積あるいは工C
工法が用いられる。The obtained drawn yarn is subjected to oil treatment, dry relaxation treatment, etc. in a conventional manner to obtain acrylic fibers. The product of knot strength and knot elongation or coefficient C is used to evaluate the pill resistance of acrylic fibers.
construction method is used.
R維の結節強度が低い場合本しくは結節伸度が低い場合
には衣料の表面に毛玉が生成した場合でも少しの外力で
毛玉を衣料から切り離して脱落させることができる。従
って毛羽、短毛が絡ま)あい毛玉が生成してもそれが大
きく成長する前に脱落するため衣料の外観を損うことは
なくなる。本発明の抗ピル性アクリル繊M1は結節強度
と結節伸度との積が20以下となり、工C工法で評価し
た抗ピル性は4級以上となる。If the knot strength of the R fibers is low, or if the knot elongation is low, even if pilling occurs on the surface of the clothing, the pill can be separated from the clothing and dropped off with a small amount of external force. Therefore, even if fuzz and short hair become entangled, the pill will fall off before it grows large, so it will not spoil the appearance of the clothing. The anti-pilling acrylic fiber M1 of the present invention has a product of knot strength and knot elongation of 20 or less, and anti-pilling properties evaluated by method C are grade 4 or higher.
以下実施例により本発明を具体的忙説明する。 The present invention will be specifically explained below with reference to Examples.
「噛」は重量部を表す。「結節強度(t/L)」「結節
伸度(憾)」はJ工5−xJlolslcよシ測定した
。"Ki" means parts by weight. "Knot strength (t/L)" and "knot elongation (lack)" were measured using J-K5-xJolslc.
から算出した。Calculated from.
から算出した(*遠心脱水処理1000GX10分)。Calculated from (*centrifugal dehydration treatment 1000GX 10 minutes).
「抗ピル性J#im維を511にカットし通常の2イン
チ紡で1152MGの紡績糸とし天竺組織の編地に製編
し、工C工法で3時間評価した。The anti-pilling J#im fiber was cut into 511 pieces and spun into a 1152 MG yarn using normal 2-inch spinning, knitted into a jersey fabric, and evaluated using the C method for 3 hours.
実施例1.比較例1
アクリロニトリル934、アクリル酸メチル64、メタ
リルスルホン酸ソーダ14からなる共重合体をジメチル
アセトアミドに溶解し表1に示すような条件下紡糸原液
を得た。この紡糸原液を湿式紡糸し、環水中で溶剤を洗
浄しながら延伸を施し特定膨潤度のウェットトウを得た
。Example 1. Comparative Example 1 A copolymer consisting of 934 acrylonitrile, 64 methyl acrylate, and 14 sodium methallylsulfonate was dissolved in dimethylacetamide to obtain a spinning stock solution under the conditions shown in Table 1. This spinning stock solution was wet-spun, and stretched while washing the solvent in ring water to obtain a wet tow with a specific degree of swelling.
続いてウェットトウに油剤を付着させ150℃の熱ロー
ラーで乾燥し、更にt 5 kg/ex”の加圧スチー
ム中で緩和処理を行い単繊維繊度が2d/fの繊維を得
た。この繊維を51■にカットし通常の2インチ紡で1
752M0の紡績糸となし、天竺組織の編地に製編し抗
ピル性を評価し結果を表1に示した。Subsequently, the wet tow was coated with an oil agent, dried with a heated roller at 150°C, and further subjected to relaxation treatment in pressurized steam at t 5 kg/ex" to obtain fibers with a single fiber fineness of 2 d/f. This fiber Cut it into 51■ and spin it with normal 2 inch spinning.
A spun yarn of 752M0 was knitted into a knitted fabric with a jersey texture and the anti-pilling properties were evaluated, and the results are shown in Table 1.
表1から甲らかなどとく原液濃度、紡糸ドラフト、膨I
IIIi度、延伸倍率、得られた櫂維の強度、結節強伸
度の積等の何れの一つが欠けて本目標とする抗ピル性が
得られない事がわかる。From Table 1, the concentration of the stock solution, spinning draft, swelling I
It can be seen that the desired pill resistance cannot be obtained due to a lack of any one of the IIIi degree, the stretching ratio, the strength of the obtained paddle fiber, and the product of knot strength and elongation.
実施例2.比較例2
アクリロニトリル934、アクリル酸メチル6憾、メタ
リルスルホン酸ソーダ1略からなる共重合体を用い、実
施例1と同様にして、但し紡糸原液に水を添加して表2
に示すような条件で紡糸実験を行い、得られたアクリル
11!維の抗ピル性を評価した。結果を表2に示した。Example 2. Comparative Example 2 A copolymer consisting of 934 acrylonitrile, 6 parts methyl acrylate, and 1 part sodium methallylsulfonate was used in the same manner as in Example 1, except that water was added to the spinning dope.
A spinning experiment was conducted under the conditions shown in , and the obtained acrylic 11! The anti-pilling properties of the fibers were evaluated. The results are shown in Table 2.
表 1
表2から明らかなごとく原液濃度、紡糸ドラフト、洗浄
・延伸糸膨潤度、延伸倍率、得られた繊維の強度、結節
強伸度の積等の何れの一つが欠けて本目標とする抗ピル
性が得られない事がわかる。Table 1 As is clear from Table 2, any one of the following factors, such as stock solution concentration, spinning draft, washing/drawing yarn swelling degree, drawing ratio, strength of the obtained fiber, product of knot strength and elongation, etc., may be lacking, resulting in a failure to achieve the target resistance. It turns out that pill-like properties cannot be obtained.
更に、紡糸原液に水を添加するととKよって繊維の断面
形状がソラ豆状から丸断面化し紡績工程での糸切れ、毛
羽等が減少した。又繊維の光沢窓が増し製品風合も向上
した。Furthermore, when water was added to the spinning dope, K caused the cross-sectional shape of the fibers to change from a bean-like shape to a round cross-section, reducing yarn breakage, fuzz, etc. during the spinning process. In addition, the glossy window of the fibers has increased and the texture of the product has also improved.
本発明で得られるアクリル繊維は、優れた杭ピル性を有
すると共に優雅な光沢窓のある風合を保持し、衣料用繊
維として有用である。The acrylic fiber obtained by the present invention has excellent pile-pilling properties and maintains an elegant glossy texture, making it useful as a textile for clothing.
特許出願人 三費レイヨン株式会社Patent applicant: Sankei Rayon Co., Ltd.
Claims (1)
系重合体を22%以下含有する紡糸原液を紡糸ドラフト
0.7〜1.4で凝固浴に湿式紡糸し、膨潤度160〜
250%で繊維化して強度3.0g/d以上、結節強度
(g/d)と結節伸度(%)の積が20以下のアクリル
繊維を製造することを特徴とする抗ピル性アクリル繊維
の製造法。 2、紡糸原液が3%以下の水を含有することを特徴とす
る請求項1記載の製造法。 3、延伸倍率1.5〜6倍で延伸を行うことを特徴とす
る請求項1記載の製造法。[Scope of Claims] 1. A spinning dope containing 90% or more of acrylonitrile and 22% or less of an acrylonitrile polymer is wet-spun in a coagulation bath at a spinning draft of 0.7 to 1.4, and the swelling degree is 160 to 160.
An anti-pilling acrylic fiber characterized by producing an acrylic fiber having a strength of 3.0 g/d or more and a product of knot strength (g/d) and knot elongation (%) of 20 or less when fiberized at 250%. Manufacturing method. 2. The manufacturing method according to claim 1, wherein the spinning dope contains 3% or less of water. 3. The manufacturing method according to claim 1, wherein the stretching is carried out at a stretching ratio of 1.5 to 6 times.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16219590A JP2958056B2 (en) | 1990-06-20 | 1990-06-20 | Manufacturing method of anti-pill acrylic fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16219590A JP2958056B2 (en) | 1990-06-20 | 1990-06-20 | Manufacturing method of anti-pill acrylic fiber |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0457909A true JPH0457909A (en) | 1992-02-25 |
| JP2958056B2 JP2958056B2 (en) | 1999-10-06 |
Family
ID=15749804
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16219590A Expired - Lifetime JP2958056B2 (en) | 1990-06-20 | 1990-06-20 | Manufacturing method of anti-pill acrylic fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2958056B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008095255A (en) * | 2006-10-16 | 2008-04-24 | Mitsubishi Rayon Co Ltd | Anti-pill acrylic fiber and production method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4955921B2 (en) * | 2004-12-24 | 2012-06-20 | 三菱レイヨン株式会社 | Anti-pill fine fineness acrylic fiber, method for producing the same, and spun yarn |
-
1990
- 1990-06-20 JP JP16219590A patent/JP2958056B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008095255A (en) * | 2006-10-16 | 2008-04-24 | Mitsubishi Rayon Co Ltd | Anti-pill acrylic fiber and production method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2958056B2 (en) | 1999-10-06 |
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