JPH083820A - Acetate conjugate fiber having latent crimp and manufacture thereof - Google Patents

Acetate conjugate fiber having latent crimp and manufacture thereof

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Publication number
JPH083820A
JPH083820A JP15815494A JP15815494A JPH083820A JP H083820 A JPH083820 A JP H083820A JP 15815494 A JP15815494 A JP 15815494A JP 15815494 A JP15815494 A JP 15815494A JP H083820 A JPH083820 A JP H083820A
Authority
JP
Japan
Prior art keywords
fiber
cellulose
component
acetate
cellulose triacetate
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
Application number
JP15815494A
Other languages
Japanese (ja)
Other versions
JP3376110B2 (en
Inventor
Yasushi Komura
恭史 香村
Akihito Toshi
彰人 都志
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP15815494A priority Critical patent/JP3376110B2/en
Publication of JPH083820A publication Critical patent/JPH083820A/en
Application granted granted Critical
Publication of JP3376110B2 publication Critical patent/JP3376110B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Multicomponent Fibers (AREA)

Abstract

PURPOSE:To obtain an acetate conjugate fiber having latent crimp, capable of exhibiting flexible soft touch and bulky feeling and at the same time having sufficient crimping characteristics. CONSTITUTION:A cellulose diacetate having an average acetate ratio of <56.2% and a cellulose triacetate having an average acetate ratio of 56.2-62.5% are subjected to side-by-side type conjugate spinning to obtain a precursor fiber having a single fiber fineness of 1.0-2.5 denier. The precursor fiber is subjected to saponification treatment with an alkali aqueous solution to obtain the objective latent crimp-having fiber which is composed of a cellulose acetate component or a cellulose component having an average acetate ratio of <48.8% and a cellulose triacetate component having an average acetate ratio of 56.2-62.5% each of which is attached to each other in a side-by-side state and has a single fiber fineness of 0.8-2.0 denier, bulkiness of >=22.0cm<3>/g and shrinkage of >=30%.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、潜在捲縮性アセテート
複合繊維及びその製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a latently crimpable acetate conjugate fiber and a method for producing the same.

【0002】[0002]

【従来の技術】アセテート繊維は、高い光沢とドライな
感触、深みのある色調、さらには他繊維との親和性に優
れているが、反面ふくらみ感、軽量感にやや欠けるとこ
ろがある。これは、アセテート繊維が乾式紡糸法により
製造されるという原糸製造の基本紡糸法に起因するもの
である。しかしながら、アセテート繊維においても、消
費者ニーズの多様化により、ふくらみ感、軽量感を有す
る繊維が求められており、このため、例えば紡糸過程で
ノズル形状を異型化し繊維を異型断面とする方法、或い
は後加工で繊維を嵩高加工する方法等が提案されている
が、これらの方法では、ふくらみ感が十分でなかった
り、或いはふくらみ感は得られてもハリ、コシが損なわ
れる場合が多い。
2. Description of the Prior Art Acetate fibers have a high gloss, a dry feel, a deep color tone, and an excellent affinity with other fibers, but on the other hand, they have a slight lack of swelling and lightness. This is due to the basic spinning method of the raw yarn production, in which the acetate fiber is produced by the dry spinning method. However, also in the acetate fiber, due to the diversification of consumer needs, a fiber having a swelling feeling and a lightweight feeling is demanded. Therefore, for example, a method of deforming the nozzle shape in the spinning process to make the fiber have an irregular cross section, or Although methods such as post-processing bulky processing of fibers have been proposed, these methods often result in insufficient swelling feeling, or even when a swelling feeling is obtained, firmness and elasticity are impaired.

【0003】そこで、濃度の異なるアセテート紡糸原液
を用い、サイドバイサイド型に複合紡糸し熱水処理によ
り捲縮付与する方法も提案(特公昭43ー25941号
公報)されているが、ある程度のふくらみ感は得られる
ものの、満足すべきふくらみ感を得るには至っていな
い。
Therefore, there has been proposed a method in which acetate spinning stock solutions having different concentrations are used for composite spinning in a side-by-side type and crimping is given by hot water treatment (Japanese Patent Publication No. 43-25941). Although it can be obtained, it does not reach a satisfactory swelling feeling.

【0004】また、酢化度の異なる2種の成分をサイド
バイサイド型に複合紡糸しアルカリ処理を施して自発捲
縮を発現させる方法もあるが、得られるアセテート複合
繊維内の高酢化度成分の成分比を大きくすると、ソフト
感は向上するが、嵩高度は十分に大きくは得られない。
一方、得られるアセテート複合繊維内の収縮部分である
低酢化度成分の成分比を大きくすると、嵩高度は大きく
は得られるが、しなやかなソフト風合いは得られ難い。
There is also a method in which two components having different acetylation degrees are composite-spun into a side-by-side type and subjected to alkali treatment to develop spontaneous crimps. When the component ratio is increased, the soft feeling is improved, but the bulkiness cannot be sufficiently increased.
On the other hand, if the component ratio of the low acetylation degree component, which is the contracted portion in the obtained acetate conjugate fiber, is increased, the bulkiness is increased, but it is difficult to obtain a supple soft texture.

【0005】さらに高酢化度成分と低酢化度成分を繊維
軸方向に沿って変動させる方法により、大きな嵩高度及
びソフト風合いを付与することも可能であるが、フィラ
メントに発現する自発捲縮の捲縮力が不十分で、織編物
の組織により十分な捲縮発現が得られない場合がある。
Further, it is possible to give a large bulky height and a soft texture by a method of varying the high acetylation component and the low acetylation component along the fiber axis direction, but the spontaneous crimping which develops in the filament. In some cases, the crimping force is insufficient and sufficient crimp expression cannot be obtained depending on the structure of the woven or knitted fabric.

【0006】[0006]

【発明が解決しようとする課題】本発明は、アセテート
複合繊維における複合成分間の酢化度差の拡大と単繊維
繊度の極細化とを組み合わせたことにあり、本発明の目
的は、しなやかなソフトな風合い及び大きなふくらみ感
を発現し、かつ十分な捲縮力を有する潜在捲縮性アセテ
ート複合繊維を提供することにある。
DISCLOSURE OF THE INVENTION The present invention is to combine the expansion of the difference in acetylation degree between the composite components in the acetate composite fiber and the ultrafineness of the single fiber fineness, and the object of the present invention is suppleness. It is an object of the present invention to provide a latently crimpable acetate conjugate fiber that exhibits a soft texture and a large bulge and has a sufficient crimping force.

【0007】[0007]

【課題を解決するための手段】本発明の要旨は、平均酢
化度48.8%未満のセルロースアセテート成分又はセ
ルロース成分と平均酢化度56.2〜62.5%のセル
ローストリアセテート成分がサイドバイサイド型に貼り
合わされ、単繊維繊度が0.8〜2.0デニールのアセ
テート複合繊維であって、かつ2.0cm3/g以上の
嵩高度及び30%以上の捲縮率を有する潜在捲縮性アセ
テート複合繊維、及び、
The gist of the present invention is that the cellulose acetate component having an average acetylation degree of less than 48.8% or the cellulose component and the cellulose triacetate component having an average acetylation degree of 56.2 to 62.5% are side by side. Latent crimpability, which is bonded to a mold, is an acetate composite fiber having a single fiber fineness of 0.8 to 2.0 denier, and has a bulkiness of 2.0 cm 3 / g or more and a crimping rate of 30% or more. Acetate composite fiber, and

【0008】平均酢化度56.2%未満のセルロースジ
アセテートと平均酢化度56.2%〜62.5%のセル
ローストリアセテートをサイドバイサイド型に複合紡糸
し、単繊維繊度を1.0〜2.5デニールとした前駆体
繊維を、アルカリ水溶液で鹸化処理することを特徴とす
る潜在捲縮性アセテート複合繊維の製造方法にある。
[0008] Cellulose diacetate having an average acetylation degree of less than 56.2% and cellulose triacetate having an average acetylation degree of 56.2% to 62.5% are composite-spun in a side-by-side type to have a single fiber fineness of 1.0 to 2 A method for producing a latently crimpable acetate conjugate fiber, which comprises subjecting a precursor fiber having a denier of 0.5 to a saponification treatment with an alkaline aqueous solution.

【0009】本発明の潜在捲縮性アセテート複合繊維
は、2種の構成成分がサイドバイサイド型に貼り合わさ
れた複合構造をなすものであり、一方の構成成分は、平
均酢化度48.8%未満のセルロースアセテート又はセ
ルロースであり、他方の構成成分は、平均酢化度56.
2〜62.5%のセルローストリアセテートである。
The latently crimpable acetate conjugate fiber of the present invention has a composite structure in which two kinds of constituent components are bonded side by side, and one constituent component has an average acetylation degree of less than 48.8%. Cellulose acetate or cellulose, and the other component has an average degree of acetylation of 56.
2 to 62.5% cellulose triacetate.

【0010】又、本発明の潜在捲縮性アセテート複合繊
維においては、その単繊維繊度が0.8〜2.0デニー
ル(以下d)であり、かつ、後述の実施例での測定方法
による2.0cm3/g以上の嵩高度及び30%以上の
捲縮率を有し、かかる大きな嵩高性及び捲縮率が、繊維
の極細繊度と相俟って、しなやかなソフトな風合い及び
ふくらみ感をもたらす。
In the latently crimpable acetate conjugate fiber of the present invention, the single fiber fineness is 0.8 to 2.0 denier (hereinafter referred to as d), and 2 according to the measuring method in Examples described later. It has a bulkiness of 0.0 cm 3 / g or more and a crimp ratio of 30% or more, and such a large bulkiness and crimp ratio, combined with the fineness of the fiber, give a supple and soft texture and a feeling of swelling. Bring

【0011】本発明の潜在捲縮性アセテート複合繊維
は、次のようにして得られる。すなわち、平均酢化度5
6.2%未満、好ましくは平均酢化度56.2%未満4
8.8%以上のセルロースジアセテートと平均酢化度5
6.2%〜62.5%のセルローストリアセテートをサ
イドバイサイド型に複合紡糸し、単繊維繊度を1.0〜
2.5dとした前駆体繊維を、アルカリ水溶液で鹸化処
理することにより得られる。
The latently crimpable acetate conjugate fiber of the present invention is obtained as follows. That is, the average degree of acetylation is 5
Less than 6.2%, preferably less than 56.2% average acetylation 4
Cellulose diacetate of 8.8% or more and average acetylation degree of 5
6.2% -62.5% of cellulose triacetate was composite-spun into a side-by-side type, and the single fiber fineness was 1.0-
It is obtained by subjecting the precursor fiber of 2.5d to saponification treatment with an alkaline aqueous solution.

【0012】アルカリ水溶液での鹸化処理により、前駆
体繊維の複合成分のうち平均酢化度56.2%未満のセ
ルロースジアセテート成分が選択的に部分鹸化減量さ
れ、その処理条件により酢化度48.8%未満の低酢化
度セルロースアセテート乃至酢化度0%のセルロースと
なる。又、このアルカリ鹸化処理でのセルロースジアセ
テート成分の部分減量により、元の前駆体繊維全体の0
〜20wt%を減量させ、単繊維繊度を0.8〜2.0
dとする。
By the saponification treatment with an alkaline aqueous solution, the cellulose diacetate component having an average degree of acetylation of less than 56.2% is selectively saponified in the composite component of the precursor fiber, and the degree of acetylation is 48 depending on the treatment conditions. A cellulose acetate having a low acetylation degree of less than 0.8% or a cellulose having an acetylation degree of 0% is obtained. In addition, due to the partial reduction of the cellulose diacetate component in this alkali saponification treatment, the total amount of the original precursor fibers was
〜20wt% is reduced and single fiber fineness is 0.8〜2.0
d.

【0013】本発明の潜在捲縮性アセテート複合繊維を
得る方法を、更に説明すると、前駆体繊維を構成するセ
ルロースジアセテート成分とセルローストリアセテート
成分の複合比(重量比)は、特に限定されるものではな
く目的に応じて設定すればよいが、好ましい複合比は、
セルロースジアセテート成分/セルローストリアセテー
ト成分=40/60〜60/40である。
The method for obtaining the latently crimpable acetate conjugate fiber of the present invention will be further described. The composite ratio (weight ratio) of the cellulose diacetate component and the cellulose triacetate component constituting the precursor fiber is particularly limited. However, the preferred composite ratio is
Cellulose diacetate component / cellulose triacetate component = 40/60 to 60/40.

【0014】前駆体繊維の製造において、本発明の単繊
維繊度0.8〜2.0dの潜在捲縮性アセテート複合繊
維を得るためには、前駆体繊維の単繊維繊度を1.0〜
2.5d、好ましくは1.2〜2.0dにしておくこと
が必要である。かかる単繊維繊度の前駆体繊維を得るた
めには、前駆体繊維の製造時に細孔径の紡糸ノズルを用
いる、紡糸から巻取りまでのドラフトを大きくする、或
いは希釈紡糸原液を用いる等の方法があるが、用いる手
段は、得られるアセテート複合繊維の糸物性や製造設備
等を考慮して決定される。
In producing the precursor fiber, in order to obtain the latently crimpable acetate conjugate fiber of the present invention having the single fiber fineness of 0.8 to 2.0 d, the single fiber fineness of the precursor fiber is 1.0 to
It is necessary to set it to 2.5d, preferably 1.2 to 2.0d. In order to obtain a precursor fiber having such a single fiber fineness, there are methods such as using a spinning nozzle having a fine pore diameter during the production of the precursor fiber, increasing a draft from spinning to winding, or using a diluted spinning dope. However, the means to be used is determined in consideration of the yarn physical properties of the obtained acetate conjugate fiber, manufacturing equipment and the like.

【0015】次いで、前駆体繊維をアルカリ水溶液で鹸
化処理することにより本発明の潜在捲縮性アセテート複
合繊維を得るが、鹸化処理は、水酸化ナトリウム、炭酸
カルシウム等のアルカリ化合物の水溶液に前駆体繊維を
浸漬する等の方法により行われる。処理条件は、アルカ
リ化合物、前駆体繊維の構成等により異なるが、水酸化
ナトリウムを使用する場合であれば、水酸化ナトリウム
5wt%未満の濃度、30〜100℃の処理温度、15
分以下の処理時間である。
Then, the latently crimpable acetate composite fiber of the present invention is obtained by subjecting the precursor fiber to saponification treatment with an aqueous alkali solution. The saponification treatment is carried out by adding the precursor to an aqueous solution of an alkali compound such as sodium hydroxide or calcium carbonate. It is carried out by a method such as dipping the fibers. The treatment conditions vary depending on the alkali compound, the composition of the precursor fiber, etc., but when sodium hydroxide is used, the concentration of sodium hydroxide is less than 5 wt%, the treatment temperature is 30 to 100 ° C.
The processing time is less than a minute.

【0016】かかるアルカリ鹸化処理により、前駆体繊
維は、そのセルロースジアセテート成分が選択的に鹸化
減量されてその酢化度がより低くなり高収縮を生じ捲縮
が発現するとともに、前駆体繊維の単繊維繊度が極細化
されているために、アルカリ鹸化処理により発現するヘ
リカルコイル様の捲縮の繊維軸方向の発現頻度がより増
大することにより、2.0cm3/g以上の嵩高度及び
30%以上の捲縮率を示す繊維となり、しなやかなソフ
トな風合い及び大きなふくらみ感を発現し、かつ十分な
捲縮力を有する本発明の潜在捲縮性アセテート複合繊維
が得られる。
By the alkali saponification treatment, the precursor fiber is selectively saponified and reduced in its cellulose diacetate component, the degree of acetylation becomes lower, high shrinkage occurs, and crimps are developed. Since the single fiber fineness is extremely thinned, the frequency of occurrence of helical coil-like crimps in the fiber axis direction, which is developed by alkali saponification treatment, is further increased, resulting in a bulk height of 2.0 cm 3 / g or more and 30 Thus, the latent crimpable acetate conjugate fiber of the present invention having a crimp ratio of not less than%, exhibiting a soft and soft texture and a large bulge and having a sufficient crimping force can be obtained.

【0017】[0017]

【実施例】以下、実施例により本発明を具体的に説明す
る。なお、実施例及び比較例におけるふくらみ感を表す
嵩高度、捲縮率及び風合いの測定方法を下記に示す。
The present invention will be described below in detail with reference to examples. The methods for measuring bulkiness, crimp ratio, and texture showing the swelling feeling in Examples and Comparative Examples are shown below.

【0018】嵩高度:試料の繊維を幅6mm、深さ3
3.5mmの溝部を有するロールの溝部に0.1g/d
の張力下に巻取り、溝部に巻取られた試料の重量Wと試
料が占める溝部の容積Vを測定し、嵩高度D(cm3
g)を式D=V/Wより算出した。 捲縮率:試料の一端を固定し、10mg/dの荷重を加
えて30秒後の試料長A、続いて1g/dの荷重を加え
て30秒後の試料長Bを測定し、捲縮率Ce(%)を式
Ce=(B−A)/B×100より算出した。 風合い:官能テストでソフト感を判定し、極めて良好な
方から順に◎、○、△、×で示した。
Bulkiness: The sample fibers are 6 mm wide and 3 deep.
0.1 g / d in the groove of the roll having the groove of 3.5 mm
The weight W of the sample wound in the groove portion and the volume V of the groove portion occupied by the sample are measured, and the bulk height D (cm 3 /
g) was calculated from the formula D = V / W. Crimping rate: One end of the sample was fixed, a sample length A after 30 seconds after applying a load of 10 mg / d, and a sample length B after 30 seconds after applying a load of 1 g / d, and crimping was performed. The rate Ce (%) was calculated from the formula Ce = (B−A) / B × 100. Texture: Softness was judged by a sensory test, and it was shown in the order of ◎, ○, △, × from the most favorable one.

【0019】(実施例1)平均酢化度61.6%のセル
ローストリアセテートと平均酢化度55.2%のセルロ
ースジアセテートをそれぞれ塩化メチレン/メタノール
(=91/9)の混合溶剤に溶解し、原液濃度22重量
%のセルローストリアセテート紡糸原液、及びセルロー
スジアセテート紡糸原液をそれぞれ調製した。これらの
紡糸原液を用い、乾式紡糸法によりセルローストリアセ
テート成分/セルロースジアセテート成分=50/50
の複合比(重量比)でサイドバイサイド型複合紡糸を行
い、50d/20フィラメント(以下f)の前駆体繊維
を得た。
Example 1 Cellulose triacetate having an average acetylation degree of 61.6% and cellulose diacetate having an average acetylation degree of 55.2% were each dissolved in a mixed solvent of methylene chloride / methanol (= 91/9). A cellulose triacetate spinning stock solution and a cellulose diacetate spinning stock solution each having a stock solution concentration of 22% by weight were prepared. Cellulose triacetate component / cellulose diacetate component = 50/50 by dry spinning using these spinning dope.
Side-by-side type composite spinning was carried out at the composite ratio (weight ratio) of to obtain a precursor fiber of 50d / 20 filament (hereinafter referred to as f).

【0020】次いで、この前駆体繊維を下記条件のアル
カリ水溶液に浸漬し鹸化処理した。 アルカリ水溶液 水酸化ナトリウム1wt%水溶液 温度 60℃ 時間 10分 浴比 1:100 得られた繊維は、酢化度0%のセルロース成分と酢化度
61.6%のセルローストリアセテート成分とがサイド
バイサイド型に貼り合わされた複合構造をなしており、
表1に繊維の実測繊度、繊維物性、嵩高度、捲縮率、風
合いを示した。
Next, this precursor fiber was dipped in an alkaline aqueous solution under the following conditions and saponified. Alkaline aqueous solution Sodium hydroxide 1 wt% aqueous solution Temperature 60 ° C Time 10 minutes Bath ratio 1: 100 The obtained fiber is composed of a cellulose component having an acetylation degree of 0% and a cellulose triacetate component having an acetylation degree of 61.6% in a side-by-side type. It has a laminated composite structure,
Table 1 shows the actually measured fineness, physical properties, bulkiness, crimp ratio, and texture of the fibers.

【0021】(実施例2)実施例1で用いたと同じセル
ローストリアセテート紡糸原液とセルロースジアセテー
ト紡糸原液を用い、乾式紡糸法によりセルローストリア
セテート成分/セルロースジアセテート成分=50/5
0の複合比でサイドバイサイド型複合紡糸を行い、40
d/20fの前駆体繊維を得た。次いで、この前駆体繊
維を実施例1と同じ条件でアルカリ鹸化処理した。得ら
れた繊維は、酢化度0%のセルロース成分と酢化度6
1.6%のセルローストリアセテート成分とがサイドバ
イサイド型に貼り合わされた複合構造をなしており、表
1に繊維の実測繊度、繊維物性、嵩高度、捲縮率、風合
いを示した。
Example 2 Using the same cellulose triacetate spinning dope and cellulose diacetate spinning dope as used in Example 1, a dry spinning method was used to prepare a cellulose triacetate component / cellulose diacetate component = 50/5.
Side-by-side type composite spinning was performed at a composite ratio of 0, and 40
A precursor fiber of d / 20f was obtained. Next, this precursor fiber was alkali-saponified under the same conditions as in Example 1. The obtained fiber contains a cellulose component having an acetylation degree of 0% and an acetylation degree of 6%.
It has a composite structure in which 1.6% of cellulose triacetate component is pasted in a side-by-side type, and Table 1 shows the actually measured fineness of fibers, fiber physical properties, bulkiness, crimp ratio, and texture.

【0022】(実施例3)実施例1で用いたと同じセル
ローストリアセテート紡糸原液とセルロースジアセテー
ト紡糸原液を用い、乾式紡糸法によりセルローストリア
セテート成分/セルロースジアセテート成分=50/5
0の複合比でサイドバイサイド型複合紡糸を行い、30
d/20fの前駆体繊維を得た。次いで、この前駆体繊
維を実施例1と同じ条件でアルカリ処理をした。得られ
た繊維は、酢化度0%のセルロース成分と酢化度61.
6%のセルローストリアセテート成分とがサイドバイサ
イド型に貼り合わされた複合構造をなしており、表1に
繊維の実測繊度、繊維物性、嵩高度、捲縮率、風合いを
示した。
Example 3 Using the same cellulose triacetate spinning dope and cellulose diacetate spinning dope as used in Example 1, a dry spinning method was used to prepare a cellulose triacetate component / cellulose diacetate component = 50/5.
Side-by-side type composite spinning was performed at a composite ratio of 0,
A precursor fiber of d / 20f was obtained. Next, this precursor fiber was alkali-treated under the same conditions as in Example 1. The obtained fiber is composed of a cellulose component having an acetylation degree of 0% and an acetylation degree of 61.
It has a composite structure in which 6% of a cellulose triacetate component is pasted in a side-by-side type, and Table 1 shows the actually measured fineness of fibers, fiber physical properties, bulkiness, crimp ratio, and texture.

【0023】(比較例1)実施例1で用いたと同じセル
ローストリアセテート紡糸原液とセルロースジアセテー
ト紡糸原液を用い、乾式紡糸法によりセルローストリア
セテート成分/セルロースジアセテート成分=50/5
0の複合比でサイドバイサイド型複合紡糸を行い、75
d/20fの前駆体繊維を得た。次いで、この前駆体繊
維を実施例1と同じ条件でアルカリ処理をした。得られ
たアセテート複合繊維は、酢化度0%のセルロース成分
と酢化度61.6%のセルローストリアセテート成分と
のサイドバイサイド型の複合構造をなしており、表1に
繊維の実測繊度、繊維物性、嵩高度、捲縮率、風合いを
示した。
(Comparative Example 1) Using the same cellulose triacetate spinning dope and cellulose diacetate spinning dope as used in Example 1, a dry spinning method was used to prepare a cellulose triacetate component / cellulose diacetate component = 50/5.
Side-by-side type composite spinning was performed at a composite ratio of 0, and
A precursor fiber of d / 20f was obtained. Next, this precursor fiber was alkali-treated under the same conditions as in Example 1. The obtained acetate conjugate fiber has a side-by-side type composite structure of a cellulose component having an acetylation degree of 0% and a cellulose triacetate component having an acetylation degree of 61.6%. , Bulk height, crimp ratio, and texture.

【0024】(比較例2)実施例1で用いたと同じセル
ローストリアセテート紡糸原液とセルロースジアセテー
ト紡糸原液を用い、乾式紡糸法によりセルローストリア
セテート成分/セルロースジアセテート成分=65/3
5の複合比でサイドバイサイド型複合紡糸を行い、75
d/20fの前駆体繊維を得た。次いで、この前駆体繊
維を実施例1と同じ条件でアルカリ処理をした。得られ
たアセテート複合繊維は、酢化度0%のセルロース成分
と酢化度61.6%のセルローストリアセテート成分と
のサイドバイサイド型の複合構造をなしており、表1に
繊維の実測繊度、繊維物性、嵩高度、捲縮率、風合いを
示した。
Comparative Example 2 Using the same cellulose triacetate spinning dope and cellulose diacetate spinning dope as used in Example 1, a dry spinning method was used to prepare cellulose triacetate component / cellulose diacetate component = 65/3.
Side-by-side type composite spinning was performed at a composite ratio of 5, and
A precursor fiber of d / 20f was obtained. Next, this precursor fiber was alkali-treated under the same conditions as in Example 1. The obtained acetate conjugate fiber has a side-by-side type composite structure of a cellulose component having an acetylation degree of 0% and a cellulose triacetate component having an acetylation degree of 61.6%. , Bulk height, crimp ratio, and texture.

【0025】(比較例3)実施例1で用いたと同じセル
ローストリアセテート紡糸原液とセルロースジアセテー
ト紡糸原液を用い、乾式紡糸法によりセルローストリア
セテート成分/セルロースジアセテート成分=35/6
5の複合比で複合紡糸を行い、75d/20fの前駆体
繊維を得た。次いで、この前駆体繊維を実施例1と同じ
条件でアルカリ処理をした。得られたアセテート複合繊
維は、酢化度0%のセルロース成分と酢化度61.6%
のセルローストリアセテート成分とのサイドバイサイド
型の複合構造をなしており、表1に繊維の実測繊度、繊
維物性、嵩高度、捲縮率、風合いを示した。
Comparative Example 3 Using the same cellulose triacetate spinning dope and cellulose diacetate spinning dope as used in Example 1, a dry spinning method was used to prepare a cellulose triacetate component / cellulose diacetate component = 35/6.
Composite spinning was carried out at a composite ratio of 5 to obtain a precursor fiber of 75d / 20f. Next, this precursor fiber was alkali-treated under the same conditions as in Example 1. The obtained acetate conjugate fiber has a cellulose component with an acetylation degree of 0% and an acetylation degree of 61.6%.
It has a side-by-side composite structure with the cellulose triacetate component, and Table 1 shows the measured fineness of the fiber, the physical properties of the fiber, the bulkiness, the crimp ratio, and the texture.

【0026】(比較例4)実施例1で用いたと同じセル
ローストリアセテート紡糸原液とセルロースジアセテー
ト紡糸原液を用い、乾式紡糸法によりセルローストリア
セテート成分/セルロースジアセテート成分=50/5
0の複合比でサイドバイサイド型複合紡糸を行い、繊維
全体の繊維断面におけるセルローストリアセテート成分
の面積比の平均値に対して繊維軸方向に±20%以上の
変動幅を有する75d/20fの前駆体繊維を得た。次
いで、この前駆体繊維を実施例1と同じ条件でアルカリ
処理をした。得られたアセテート複合繊維は、酢化度0
%のセルロース成分と酢化度61.6%のセルロースト
リアセテート成分とのサイドバイサイド型の複合構造を
なしており、表1に繊維の実測繊度、繊維物性、嵩高
度、捲縮率、風合いを示した。
(Comparative Example 4) Using the same cellulose triacetate spinning dope and cellulose diacetate spinning dope as used in Example 1, a dry spinning method was used to prepare a cellulose triacetate component / cellulose diacetate component = 50/5.
Side-by-side type composite spinning was performed at a composite ratio of 0, and a precursor fiber of 75d / 20f having a fluctuation range of ± 20% or more in the fiber axis direction with respect to the average value of the area ratio of the cellulose triacetate component in the fiber cross section of the entire fiber. Got Next, this precursor fiber was alkali-treated under the same conditions as in Example 1. The obtained acetate conjugate fiber has a degree of acetylation of 0.
% Cellulose component and a cellulose triacetate component having a degree of acetylation of 61.6% have a side-by-side composite structure, and Table 1 shows measured fiber fineness, fiber physical properties, bulk height, crimp ratio, and texture. .

【0027】(比較例5)従来のアセテート繊維の製造
方法に従って、平均酢化度61.6%のセルローストリ
アセテートを塩化メチレン/メタノール=91/9の混
合溶剤に溶解し、原液濃度21.95重量%のセルロー
ストリアセテート紡糸原液を調製した。この紡糸原液を
用いて乾式紡糸法により75d/20fのセルロースト
リアセテート繊維を得た。表1に繊維の実測繊度、繊維
物性、嵩高度、風合いを示した。
Comparative Example 5 Cellulose triacetate having an average degree of acetylation of 61.6% was dissolved in a mixed solvent of methylene chloride / methanol = 91/9 according to a conventional method for producing acetate fibers, and a stock solution concentration was 21.95% by weight. % Cellulose triacetate spinning stock solution was prepared. Using this spinning dope, a cellulose triacetate fiber of 75d / 20f was obtained by a dry spinning method. Table 1 shows the actually measured fineness, physical properties, bulkiness, and texture of the fibers.

【0028】[0028]

【表1】 [Table 1]

【0029】実施例1〜3の本発明の繊維は、強伸度が
比較例5の従来のトリアセテート繊維と比較して若干低
いが、実用上は全く問題無いものであった。又、本発明
の繊維は、比較例1〜3の単繊維繊度が2.5dを超え
る複合繊維から得られる繊維と比較して、嵩高性、捲縮
特性、風合いが共に優れたものとなっている。また、比
較例4の構成成分の面積比の変動が有る複合繊維から得
られる繊維と比較しても、嵩高性、風合いは同程度であ
るが、捲縮特性が優れており、しなやかなソフトな風合
い及び良好なふくらみ感を発現し、かつ大きな捲縮力を
有するものであった。
The fibers of Examples 1 to 3 of the present invention have a slightly lower tenacity and elongation than the conventional triacetate fiber of Comparative Example 5, but there was no problem in practical use. Further, the fiber of the present invention is excellent in bulkiness, crimping property, and texture as compared with the fiber obtained from the composite fiber of Comparative Examples 1 to 3 having a single fiber fineness of more than 2.5 d. There is. Further, as compared with the fiber obtained from the composite fiber in which the area ratio of the constituent components of Comparative Example 4 varies, the bulkiness and the texture are about the same, but the crimping property is excellent and it is supple and soft. It had a good texture and a good swelling feeling, and had a large crimping force.

【0030】[0030]

【発明の効果】本発明の潜在捲縮性アセテート複合繊維
は、従来のアセテート繊維の有するドライでシルキー調
な風合いとは全く異なり、ソフトな風合い及び良好なふ
くらみ感を有し、かつ単繊維繊度を極細化することによ
り、しなやかなソフトな風合い、大きな嵩高性及び良好
な捲縮力を同時に具備するものであり、本発明は、アセ
テート繊維としての用途を拡大することを可能とするも
ので、その価値は極めて大である。
EFFECT OF THE INVENTION The latently crimpable acetate conjugate fiber of the present invention has a soft texture and a good swelling feeling, which is completely different from the dry and silky texture of the conventional acetate fiber, and has a single fiber fineness. By ultra-fine, which has a supple and soft texture, large bulkiness and good crimping force at the same time, the present invention, it is possible to expand the application as an acetate fiber, Its value is extremely large.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 平均酢化度48.8%未満のセルロース
アセテート成分又はセルロース成分と平均酢化度56.
2〜62.5%のセルローストリアセテート成分がサイ
ドバイサイド型に貼り合わされ、単繊維繊度が0.8〜
2.0デニールのアセテート複合繊維であって、かつ
2.0cm3/g以上の嵩高度及び30%以上の捲縮率
を有する潜在捲縮性アセテート複合繊維。
1. A cellulose acetate component or cellulose component having an average acetylation degree of less than 48.8% and an average acetylation degree of 56.
2-62.5% of cellulose triacetate component is pasted on the side-by-side type, and the single fiber fineness is 0.8-
A latent crimpable acetate conjugate fiber which is a 2.0 denier acetate conjugate fiber and has a bulkiness of 2.0 cm 3 / g or more and a crimp rate of 30% or more.
【請求項2】 平均酢化度56.2%未満のセルロース
ジアセテートと平均酢化度56.2%〜62.5%のセ
ルローストリアセテートをサイドバイサイド型に複合紡
糸し、単繊維繊度を1.0〜2.5デニールとしたアセ
テート複合前駆体繊維を、アルカリ水溶液で鹸化処理す
ることを特徴とする潜在捲縮性アセテート複合繊維の製
造方法。
2. A side-by-side composite spinning of cellulose diacetate having an average acetylation degree of less than 56.2% and cellulose triacetate having an average acetylation degree of 56.2% to 62.5% is performed to obtain a single fiber fineness of 1.0. A method for producing a latently crimpable acetate conjugate fiber, which comprises subjecting an acetate conjugate precursor fiber having a denier of about 2.5 to saponification treatment with an alkaline aqueous solution.
JP15815494A 1994-06-17 1994-06-17 Latent crimpable acetate composite fiber and method for producing the same Expired - Lifetime JP3376110B2 (en)

Priority Applications (1)

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JP15815494A JP3376110B2 (en) 1994-06-17 1994-06-17 Latent crimpable acetate composite fiber and method for producing the same

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Application Number Priority Date Filing Date Title
JP15815494A JP3376110B2 (en) 1994-06-17 1994-06-17 Latent crimpable acetate composite fiber and method for producing the same

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Publication Number Publication Date
JPH083820A true JPH083820A (en) 1996-01-09
JP3376110B2 JP3376110B2 (en) 2003-02-10

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Country Link
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002075029A1 (en) * 2001-03-21 2002-09-26 Sk Chemicals Co., Ltd Method for producing cellulose/cellulose triacetate fabrics

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002075029A1 (en) * 2001-03-21 2002-09-26 Sk Chemicals Co., Ltd Method for producing cellulose/cellulose triacetate fabrics

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