JPH05148709A - Acrylic modified cross section fiber and its production - Google Patents
Acrylic modified cross section fiber and its productionInfo
- Publication number
- JPH05148709A JPH05148709A JP34005591A JP34005591A JPH05148709A JP H05148709 A JPH05148709 A JP H05148709A JP 34005591 A JP34005591 A JP 34005591A JP 34005591 A JP34005591 A JP 34005591A JP H05148709 A JPH05148709 A JP H05148709A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- spinning
- modified cross
- monomer
- acrylonitrile
- 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
- 239000000835 fiber Substances 0.000 title claims abstract description 57
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims description 13
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000000178 monomer Substances 0.000 claims abstract description 14
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000005345 coagulation Methods 0.000 claims abstract description 7
- 230000015271 coagulation Effects 0.000 claims abstract description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 7
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 7
- 239000002904 solvent Substances 0.000 claims abstract description 6
- 238000004804 winding Methods 0.000 claims abstract description 5
- 238000002166 wet spinning Methods 0.000 claims abstract description 4
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract description 8
- 238000009987 spinning Methods 0.000 abstract description 8
- 238000010521 absorption reaction Methods 0.000 abstract description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract description 4
- 239000011148 porous material Substances 0.000 abstract description 4
- 238000004040 coloring Methods 0.000 abstract description 3
- 238000010528 free radical solution polymerization reaction Methods 0.000 abstract description 3
- 239000000203 mixture Substances 0.000 abstract description 3
- 229920006243 acrylic copolymer Polymers 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 2
- 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 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 229920002972 Acrylic fiber Polymers 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 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
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- JHUFGBSGINLPOW-UHFFFAOYSA-N 3-chloro-4-(trifluoromethoxy)benzoyl cyanide Chemical compound FC(F)(F)OC1=CC=C(C(=O)C#N)C=C1Cl JHUFGBSGINLPOW-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- RYPYDIHMPGBBJN-UHFFFAOYSA-M sodium;2-methyl-1-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].CC(C)C(S([O-])(=O)=O)NC(=O)C=C RYPYDIHMPGBBJN-UHFFFAOYSA-M 0.000 description 1
- 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 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 1
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Landscapes
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
- Artificial Filaments (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、繊維表面に筋状の開孔
部を有するアクリル系異形断面繊維に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an acrylic modified cross-section fiber having streak-shaped openings on the fiber surface.
【0002】[0002]
【従来の技術】アクリル系繊維は従来、ウールライクな
風合いを持ち、しかも嵩高性及び発色性に優れているこ
とから、寝装品,カーペット,マット,ニット商品等の
素材として広く用いられてきた。しかし、吸水性不足や
サラッとした風合い(シャリ感)が不足している事から
春,夏物素材への利用はかなり遅れている。アクリル繊
維に春,夏物素材に適する吸水性を持たせるため繊維内
部を多孔質なものあるいは中空を形成するなどの方法が
試みられ、これらの技術としては紡糸原液に異種ポリマ
ーをブレンドし、相分離現象で生じたマクロボイドを残
す、あるいはC型,U型,鞘芯型更には特開昭57−1
67409号公報に見られる様な凹凸を有する口金を用
いて紡糸する事をあげることができる。しかし、これら
の方法により得られた繊維は吸水性は満足出来ても、発
色性、シャリ感は充分改善されているとは言えない。特
に異形断面繊維については孔が複雑になり口金設計上3
デニール以下の繊維を得るのは困難である。2. Description of the Related Art Acrylic fibers have hitherto been widely used as materials for bedding products, carpets, mats, knit products and the like because they have a wool-like texture and are excellent in bulkiness and color development. However, due to lack of water absorbency and lack of dry texture (sharpness), its use for spring and summer materials has been considerably delayed. In order to make the acrylic fiber absorb water suitable for spring and summer materials, methods such as forming a porous or hollow inside of the fiber have been tried. These techniques include blending different kinds of polymers in the spinning dope and phase separation. Macro voids caused by the phenomenon are left, or C-type, U-type, sheath-core type and further JP-A-57-1
Spinning can be performed using a spinneret having irregularities as disclosed in Japanese Patent No. 67409. However, although the fibers obtained by these methods have satisfactory water absorbency, it cannot be said that the coloring property and the sharpness are sufficiently improved. Especially for modified cross-section fibers, the hole becomes complicated and
It is difficult to obtain fibers below denier.
【0003】[0003]
【発明が解決しようとする課題】本発明者らはかかる現
状に鑑み、鋭意検討の結果、本発明に到達した。本発明
の目的は春夏物用素材に適する吸水性、シャリ感、発色
性に優れた繊維表面に筋状開孔部を有するアクリル系異
形断面繊維を提供する事にある。ここで言うシャリ感と
は繊維間摩擦が高い事によるものである。本発明の他の
目的は上記アクリル系異形断面繊維を工業的容易に製造
する方法を提供する事にある。DISCLOSURE OF THE INVENTION The present inventors have arrived at the present invention as a result of intensive studies in view of the present situation. An object of the present invention is to provide an acrylic modified cross-section fiber having a streak-shaped opening portion on the surface of the fiber, which is suitable for a material for spring and summer and has excellent water absorbency, sharpness and color development. The crispness referred to here is due to the high friction between fibers. Another object of the present invention is to provide a method for industrially easily producing the above-mentioned acrylic modified cross-section fiber.
【0004】[0004]
【課題を解決するための手段】本発明は繊維表面に幅
0.2〜2μ、長さが1〜10μの繊維軸方向に開孔部
を有し、その開孔部が繊維の中心部に向って空孔を形成
しており、かつ該繊維の単繊維乾強度が3.0g/d以
上、結節強度が1.5g/d以上である事を特徴とする
アクリル系異形断面繊維にある。また、その製造方法
は、80重量%以上96重量%以下のアクリロニトリル
と20重量%以下のビニル系モノマー及びスルホン酸基
含有モノマーを溶液重合させ、孔形状が正三角形型の口
金を用いて、溶剤濃度50〜55%の凝固浴に湿式紡糸
し、巻取り速度/吐出線速度の比が0.8〜1.5で引
き取ることを特徴としている。According to the present invention, a fiber surface is provided with an opening portion having a width of 0.2 to 2 µ and a length of 1 to 10 µ in the axial direction of the fiber, and the opening portion is provided at the center of the fiber. The acrylic-based modified cross-section fiber is characterized in that pores are formed in the opposite direction, and the single fiber dry strength of the fiber is 3.0 g / d or more and the knot strength is 1.5 g / d or more. Further, the production method is a solution polymerization of 80 wt% or more and 96 wt% or less of acrylonitrile and 20 wt% or less of a vinyl-based monomer and a sulfonic acid group-containing monomer, and using a die having a regular triangular shape as a solvent. It is characterized in that wet spinning is carried out in a coagulation bath having a concentration of 50 to 55%, and winding is carried out at a winding speed / discharge linear velocity ratio of 0.8 to 1.5.
【0005】以下、本発明の構成要件について詳述す
る。本発明の繊維表面に有する開孔部は幅0.2〜2
μ、長さ1〜10μの繊維軸方向に長い開孔部で吸水
性,保水性が有利となり本発明の効果を発揮する。その
原因は定かでないが通常の丸〜楕円のマクロボイドより
も筋状の開孔部の方が繊維表面上、繊維内部での水分状
態が安定するためと思われる。又本発明のアクリル系異
形断面繊維は、単繊維強度が3.0g/d以上、結節強
度が1.5g/d以上であり、それ以下であると後加工
性が低下し、著しく商品価値が下がる。The constituent features of the present invention will be described in detail below. The opening portion of the fiber surface of the present invention has a width of 0.2 to 2
The water absorption and water retention are advantageous in the pores having a length of .mu. and a length of 1 to 10 .mu. The reason for this is not clear, but it is considered that the streak-shaped openings are more stable in the water state on the fiber surface and inside the fibers than in ordinary round to elliptical macrovoids. The acrylic modified cross-section fiber of the present invention has a single fiber strength of 3.0 g / d or more and a knot strength of 1.5 g / d or more. Go down.
【0006】次に、本発明のアクリル系異形断面繊維の
製造方法について述べる。本発明において、80重量%
以上96重量%以下のアクリロニトリルと20重量%以
下のビニル系モノマー及びスルホン酸基含有モノマーの
共重合体を使用する。ビニル系モノマーとしてはアクリ
ル酸,メタクリル酸,或いはこれらのアルキルエステル
類,酢酸ビニル,塩化ビニル,塩化ビニリデン,アリル
スルホン酸ソーダ,メタリルスルホン酸ソーダ,ビニル
スルホン酸ソーダ,スチレンスルホン酸ソーダ,2−ア
クリルアミド−2−メチルプロパンスルホン酸ソーダな
どが挙げられる。アクリロニトリルの含有量が80重量
%未満では通常の物性は得られず、96重量%より多く
なると発色性が劣る。又、スルホン酸基含有モノマーは
0.3〜5重量%共重合される事が好ましい。次に上記
共重合体の重合方法は通常知られているビニル系単量体
の重合方式であればいずれでも良く、溶液重合が品質、
コスト的に好ましい。本発明において使用する溶剤は、
ジメチルホルムアミド,ジメチルアセトアミド,ジメチ
ルスルホキシド,その他無機系溶剤が挙げられるが、繊
維表面に開孔部を持たせるには有機系溶剤が良く、15
〜30%の濃度で紡糸原液を調整する。Next, a method for producing the acrylic modified cross-section fiber of the present invention will be described. In the present invention, 80% by weight
The copolymer of 96% by weight or less of acrylonitrile and 20% by weight or less of a vinyl monomer and a sulfonic acid group-containing monomer is used. Vinyl-based monomers include acrylic acid, methacrylic acid, or their alkyl esters, vinyl acetate, vinyl chloride, vinylidene chloride, sodium allyl sulfonate, sodium methallyl sulfonate, sodium vinyl sulfonate, sodium styrene sulfonate, 2- Examples thereof include sodium acrylamido-2-methylpropane sulfonate. If the content of acrylonitrile is less than 80% by weight, normal physical properties cannot be obtained, and if it exceeds 96% by weight, the color developability is poor. The sulfonic acid group-containing monomer is preferably copolymerized in an amount of 0.3 to 5% by weight. Next, the polymerization method of the copolymer may be any conventionally known polymerization method of vinyl-based monomers, and solution polymerization is a quality,
Cost effective. The solvent used in the present invention,
Examples include dimethylformamide, dimethylacetamide, dimethylsulfoxide, and other inorganic solvents, but organic solvents are preferred to give open areas on the fiber surface.
Prepare the spinning dope at a concentration of ~ 30%.
【0007】次いで本発明で規定した正三角形型断面を
有する口金を用いて湿式紡糸される。孔面積は繊維のデ
ニール数に合わせたものを適宜選択する。本発明の凝固
浴濃度は、溶剤が50〜55%,水・アルコール等の凝
固剤が50〜45%の組成である。溶剤濃度が50%未
満、又は55%を越えると可紡性が劣り、得られた繊維
の表面に本発明の様な開孔部は見られない。Next, wet spinning is performed using a spinneret having an equilateral triangular cross section defined in the present invention. The pore area is appropriately selected according to the denier of the fiber. The coagulation bath concentration of the present invention is such that the solvent is 50 to 55% and the coagulant such as water or alcohol is 50 to 45%. If the solvent concentration is less than 50% or more than 55%, the spinnability is poor and the surface of the obtained fiber does not have the openings as in the present invention.
【0008】巻取り速度/吐出線速度の比(以下i価と
表記)が0.8〜1.5で引き取る。本発明の繊維を得
る上でi価は重要なファクターである。i価が0.8未
満で得られた繊維は、断面形状が円形に近くなり充分な
繊維間摩擦は得られない。逆に1.5を越えると凝固浴
中での切れが多発し、操業が困難になる。凝固浴より導
出された凝固糸条は、水洗又は水洗と同時に延伸、延伸
後水洗、又は水洗後延伸等の処理をした後、乾燥緻密化
させ、更に機械捲縮を付与させ種々の高次加工を施す。It is taken up when the ratio of winding speed / ejection linear velocity (hereinafter referred to as i value) is 0.8 to 1.5. The i-value is an important factor in obtaining the fiber of the present invention. The fibers obtained with an i-value of less than 0.8 have a cross-sectional shape close to a circle, and sufficient inter-fiber friction cannot be obtained. On the other hand, if it exceeds 1.5, breakage occurs frequently in the coagulation bath, making operation difficult. The coagulated yarn drawn out from the coagulation bath is subjected to treatments such as drawing with water or washing with water, drawing after drawing, washing with water, or drawing after washing with water, followed by drying and densification, and further mechanical crimping for various higher-order processing. Apply.
【0009】[0009]
【実施例】以下、本発明の実施例について具体的に説明
すると共に、比較例を挙げ、本発明の繊維が優れた特性
を有する事を明らかにする。尚、本発明の吸水性はDI
N−53814で、シャリ感(繊維間摩擦)はロッシェ
ルド社(製)Fメーターを用いて各々測定した。又、発
色性の評価はカチオン染料で浴比1:50、100℃で
60分間染色した結果、肉眼判定で5段階(通常のアク
リル系繊維を3級にした)評価した。[Examples] Examples of the present invention will be specifically described below, and Comparative Examples will be given to clarify that the fibers of the present invention have excellent properties. The water absorption of the present invention is DI
With N-53814, the sharpness (friction between fibers) was measured using an F meter of Rochelled Co. (manufactured by). The coloring property was evaluated by categorizing it with a cationic dye at a bath ratio of 1:50 at 100 ° C. for 60 minutes, and the result was evaluated by the naked eye in five grades (ordinary acrylic fiber was grade 3).
【0010】実施例1〜3、比較例1〜3 アクリロニトリル/アクリル酸メチル/2−アクリルア
ミド−2−メチルプロパンスルホン酸ソーダ=92/7
/1の組成から成るアクリル系共重合体をDMFに23
重量%の濃度で溶解した溶液を紡糸原液とした。これを
孔形状1辺0.14mmの正三角形で35000ホール
の口金を通して表1記載の凝固浴、i価で紡糸し、その
後第2浴で5倍延伸した。その後更に水洗、前オイル付
与、前乾燥、後オイル付与、クリンプ付与、セット、後
乾燥して3デニールのアクリル系異形断面繊維を得た。
各々の繊維の吸水性、繊維間摩擦、発色性の測定値を表
1に併記した。Examples 1 to 3 and Comparative Examples 1 to 3 acrylonitrile / methyl acrylate / 2-acrylamido-2-methylpropanesulfonic acid soda = 92/7
Acrylic copolymer of composition / 1/23 in DMF
A solution dissolved at a concentration of wt% was used as a spinning dope. This was spun into a coagulation bath having an i-value shown in Table 1 through a spinneret having a hole shape of 0.14 mm on a side of 35000 holes and then stretched 5 times in a second bath. Then, it was further washed with water, pre-oiled, pre-dried, post-oiled, crimped, set and post-dried to obtain a 3-denier acrylic modified cross-section fiber.
Table 1 also shows measured values of water absorption, inter-fiber friction, and color development of each fiber.
【0011】[0011]
【表1】 [Table 1]
【0012】更に図1、図2は実施例1で得られた繊維
の断面及び側面を示す写真、図3に比較例1で得られた
繊維の断面を示す写真を示した。比較例2は繊維間での
膠着が見られた。尚、比較例3は通常の円形の孔形状の
口金を使って紡糸したものである。Further, FIGS. 1 and 2 show photographs showing a cross section and a side surface of the fiber obtained in Example 1, and FIG. 3 shows a photograph showing a cross section of the fiber obtained in Comparative Example 1. In Comparative Example 2, adhesion between fibers was observed. Incidentally, Comparative Example 3 was spun using a spinneret having an ordinary circular hole shape.
【0013】[0013]
【発明の効果】本発明のアクリル系異形断面繊維は繊維
表面に筋状のマクロボイドを有し、優れた吸水性、シャ
リ感、発色性を有し春夏物用素材に適した繊維である。
更に単繊維乾強度が3.0g/d以上、結節強度が1.
5g/d以上であり、通常のアクリル系合成繊維の繊維
性能をそのまま有するので、高次加工での操業性が著し
く落ちるという事は無く紡績等の高次加工にも優れ、工
業的容易に製造出来る。INDUSTRIAL APPLICABILITY The acrylic modified cross-section fiber of the present invention has streak-like macrovoids on the fiber surface, has excellent water absorption, sharpness, and color developability and is suitable for spring-summer material. ..
Further, the single fiber dry strength is 3.0 g / d or more, and the knot strength is 1.
Since it is 5 g / d or more and has the fiber performance of ordinary acrylic synthetic fibers as it is, the operability in high-order processing is not significantly deteriorated, and it is excellent in high-order processing such as spinning, and easily manufactured industrially. I can.
【0014】[0014]
【図1】本発明の実施例1で得られた繊維の断面を示す
写真である。FIG. 1 is a photograph showing a cross section of a fiber obtained in Example 1 of the present invention.
【図2】本発明の実施例1で得られた繊維の側面を示す
写真である。FIG. 2 is a photograph showing a side surface of the fiber obtained in Example 1 of the present invention.
【図3】比較例1で得られた繊維の断面を示す写真であ
る。FIG. 3 is a photograph showing a cross section of the fiber obtained in Comparative Example 1.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 D01F 6/40 7199−3B ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location D01F 6/40 7199-3B
Claims (2)
10μの繊維軸方向に開孔部を有し、その開孔部が繊維
の中心部に向って空孔を形成しており、かつ該繊維の単
繊維乾強度が3.0g/d以上、結節強度が1.5g/
d以上である事を特徴とするアクリル系異形断面繊維。1. A fiber surface having a width of 0.2 to 2 μ and a length of 1 to
10 μm has an opening in the axial direction of the fiber, the opening forms a hole toward the center of the fiber, and the single fiber dry strength of the fiber is 3.0 g / d or more; Strength is 1.5g /
Acrylic-based modified cross-section fiber characterized by being d or more.
ロニトリルと20重量%以下のビニル系モノマー及びス
ルホン酸基含有モノマーを溶液重合させ、孔形状が正三
角形型の口金を用いて、溶剤濃度50〜55%の凝固浴
に湿式紡糸し、巻取り速度/吐出線速度の比が0.8〜
1.5で引き取ることを特徴とするアクリル系異形断面
繊維の製造方法。2. A solution of acrylonitrile in an amount of 80% by weight or more and 96% by weight or less and a vinyl monomer or a sulfonic acid group-containing monomer in an amount of 20% by weight or less is solution-polymerized, and a solvent concentration of 50 is obtained by using a die having an equilateral triangle shape. Wet spinning in a coagulation bath of ~ 55% and the ratio of winding speed / discharge linear speed is 0.8 ~.
A method for producing an acrylic modified cross-section fiber, characterized in that the fiber is collected at 1.5.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34005591A JPH05148709A (en) | 1991-11-28 | 1991-11-28 | Acrylic modified cross section fiber and its production |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34005591A JPH05148709A (en) | 1991-11-28 | 1991-11-28 | Acrylic modified cross section fiber and its production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH05148709A true JPH05148709A (en) | 1993-06-15 |
Family
ID=18333295
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP34005591A Pending JPH05148709A (en) | 1991-11-28 | 1991-11-28 | Acrylic modified cross section fiber and its production |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH05148709A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001000910A1 (en) * | 1999-06-25 | 2001-01-04 | Mitsubishi Rayon Co., Ltd. | Acrylonitrile-based synthetic fiber and method for production thereof |
| JP2008285778A (en) * | 2007-05-16 | 2008-11-27 | Mitsubishi Rayon Co Ltd | Acrylic triangular cross-section fiber and manufacturing method thereof |
| WO2016067967A1 (en) * | 2014-10-28 | 2016-05-06 | 東レ株式会社 | Porous fibers, adsorbent material, and purification column |
| JPWO2017188110A1 (en) * | 2016-04-27 | 2019-03-07 | 東レ株式会社 | Porous fiber, adsorbent material and purification column |
| JP2020157293A (en) * | 2019-03-19 | 2020-10-01 | 東レ株式会社 | Porous fiber, adsorbent material and purification column |
-
1991
- 1991-11-28 JP JP34005591A patent/JPH05148709A/en active Pending
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001000910A1 (en) * | 1999-06-25 | 2001-01-04 | Mitsubishi Rayon Co., Ltd. | Acrylonitrile-based synthetic fiber and method for production thereof |
| US6610403B1 (en) | 1999-06-25 | 2003-08-26 | Mitsubishi Rayon Co., Ltd. | Acrylonitrile-based synthetic fiber and method for production thereof |
| US6696156B2 (en) | 1999-06-25 | 2004-02-24 | Mitsubishi Rayon Co., Ltd. | Acrylic fiber and a manufacturing process therefor |
| US6733881B2 (en) | 1999-06-25 | 2004-05-11 | Mitsubishi Rayon Co., Ltd. | Acrylic fiber and a manufacturing process therefor |
| JP2008285778A (en) * | 2007-05-16 | 2008-11-27 | Mitsubishi Rayon Co Ltd | Acrylic triangular cross-section fiber and manufacturing method thereof |
| WO2016067967A1 (en) * | 2014-10-28 | 2016-05-06 | 東レ株式会社 | Porous fibers, adsorbent material, and purification column |
| US10265678B2 (en) | 2014-10-28 | 2019-04-23 | Toray Industries, Inc. | Porous fibers, adsorbent material, and purification column |
| JPWO2017188110A1 (en) * | 2016-04-27 | 2019-03-07 | 東レ株式会社 | Porous fiber, adsorbent material and purification column |
| EP3450596A4 (en) * | 2016-04-27 | 2019-11-27 | Toray Industries, Inc. | POROUS FIBER, ABSORBENT MATERIAL AND PURIFICATION COLUMN |
| JP2020157293A (en) * | 2019-03-19 | 2020-10-01 | 東レ株式会社 | Porous fiber, adsorbent material and purification column |
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