JP4943371B2 - Method for producing cellulose acetate mixed yarn - Google Patents
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- JP4943371B2 JP4943371B2 JP2008107152A JP2008107152A JP4943371B2 JP 4943371 B2 JP4943371 B2 JP 4943371B2 JP 2008107152 A JP2008107152 A JP 2008107152A JP 2008107152 A JP2008107152 A JP 2008107152A JP 4943371 B2 JP4943371 B2 JP 4943371B2
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Description
本発明は、嵩高性と風合いに優れた特徴を有する、セルロースアセテート混繊糸の製造方法に関する。 The present invention relates to a method for producing a cellulose acetate mixed yarn having characteristics excellent in bulkiness and texture.
セルロースアセテート繊維は主原料が天然パルプであり、半合成繊維といわれ天然繊維の特徴も併せ持つ特徴的な繊維である。即ち、セルロースアセテート繊維は優雅な光沢、深みのある色調、発色性、ドライ感、更には適度な吸湿性等の衣料用繊維として数多くの優れた特性を有することから、他の合成繊維とは異なった高級衣料用素材として位置付けられてきた。
一方で、特許文献1には、皺になりにくくふっくらとした嵩高・軽量感が付与されたセルロースアセテート繊維素材を提供することを目的として、後加工での熱水処理時にセルロースアセテート繊維を伸長させる方法が記載されている。
Cellulose acetate fiber is a characteristic fiber that is mainly made of natural pulp and is said to be semi-synthetic fiber and also has the characteristics of natural fiber. That is, cellulose acetate fiber has many excellent properties as a fiber for clothing such as elegant luster, deep color tone, color development, dry feeling, and moderate moisture absorption, so it is different from other synthetic fibers. It has been positioned as a luxury clothing material.
On the other hand, in Patent Document 1, for the purpose of providing a cellulose acetate fiber material imparted with a bulky and lightweight feeling that is less likely to become wrinkles, the cellulose acetate fiber is elongated at the time of hydrothermal treatment in post-processing. A method is described.
しかしながら、特許文献1に記載された実施例においては伸長率(BWS)が5%未満であり、嵩高性及びソフトな風合いという点では効果が少なく、消費者ニーズの多様化に合わせた、極度な嵩高性やソフト差の表現は困難であった。
また、伸長性の異なる他繊維との混繊加工によって得られるものであり、紡糸工程で巻き取られた繊維束がそのまま効果を発揮するものではなかった。従って、後加工工程の手間や工程中での不良発生などのリスクがある。
However, in the example described in Patent Document 1, the elongation (BWS) is less than 5%, and is less effective in terms of bulkiness and soft texture, and is extremely adapted to the diversification of consumer needs. It was difficult to express bulkiness and soft differences.
Moreover, it was obtained by blending with other fibers having different extensibility, and the fiber bundle wound in the spinning process did not exhibit the effect as it is. Therefore, there is a risk of trouble in the post-processing process and occurrence of defects in the process.
本発明の要旨は、ジアセテート繊維とトリアセテート繊維からなる混繊糸であり具体的には下記(1)〜(3)を満たす条件にてジアセテート繊維とトリアセテート繊維を同時に紡出し、捲き取る混繊糸の製造方法にある。
(1)0.15<Vf/Vja<0.50、且つ、1200<Vja<1650
(2)0.15<Vf/Vjb<1.20、且つ、200<Vjb<1650
(3)300≦Vf≦700
(収縮率が負の値とは、伸長していることを示す。)
式中、Vfは紡出時の引き取り速度(m/分)、Vjaは、ジアセテート繊維の紡糸原液の紡糸ノズルからの吐出線速度(m/分)、Vjbは、トリアセテート繊維の紡糸原液の紡糸ノズルからの吐出線速度(m/分)を示す。
The gist of the present invention is a blended yarn composed of diacetate fiber and triacetate fiber, and specifically, a blended yarn in which diacetate fiber and triacetate fiber are spun at the same time under the conditions satisfying the following (1) to (3). It exists in the manufacturing method of a fiber yarn.
(1) 0.15 <Vf / Vja <0.50 and 1200 <Vja <1650
(2) 0.15 <Vf / Vjb <1.20 and 200 <Vjb <1650
(3) 300 ≦ Vf ≦ 700
(A negative value for the shrinkage indicates that the shrinkage is expanding.)
In the formula, Vf is the take-up speed during spinning (m / min), Vja is the discharge linear speed from the spinning nozzle of the spinning solution of diacetate fiber (m / min), and Vjb is the spinning of the spinning solution of triacetate fiber. The discharge linear velocity (m / min) from the nozzle is shown.
本発明の混繊糸は、ジアセテート繊維とトリアセテート繊維の両素材を紡糸時に混繊することで嵩高性と風合いに優れたセルロースアセテート混繊糸を効率的に混繊できる。 The blended yarn of the present invention can efficiently blend a cellulose acetate blended yarn excellent in bulkiness and texture by blending both materials of diacetate fiber and triacetate fiber at the time of spinning.
本発明のセルロースアセテート混繊糸は、ジアセテート繊維とトリアセテート繊維は下記(1)〜(3)を満たす条件にて製造することが必要である。
(1)0.15<Vf/Vja<0.50、且つ、1200<Vja<1650
(2)0.15<Vf/Vjb<1.20、且つ、200<Vjb<1650
(3)300≦Vf≦700
式中、Vfは紡出時の引き取り速度(m/分)、Vjaは、ジアセテート繊維の紡糸原液の紡糸ノズルからの吐出線速度(m/分)、Vjbは、トリアセテート繊維の紡糸原液の紡糸ノズルからの吐出線速度(m/分)を示す。
In the cellulose acetate mixed yarn of the present invention, the diacetate fiber and the triacetate fiber must be produced under the conditions satisfying the following (1) to (3).
(1) 0.15 <Vf / Vja <0.50 and 1200 <Vja <1650
(2) 0.15 <Vf / Vjb <1.20 and 200 <Vjb <1650
(3) 300 ≦ Vf ≦ 700
In the formula, Vf is the take-up speed during spinning (m / min), Vja is the discharge linear speed from the spinning nozzle of the spinning solution of diacetate fiber (m / min), and Vjb is the spinning of the spinning solution of triacetate fiber. The discharge linear velocity (m / min) from the nozzle is shown.
本発明を実施するに当たり、Vf/Vjaが0.15以下の場合、及びVf/Vjaが0.50以上の場合、引き取り速度に乾燥挙動が追いつかず、連続紡糸が不安定となり好ましくない。
また、Vjaが1200以下の場合、繊維軸方向への十分な乾燥歪が形成されず、目標とする伸長率が得られない。更に、Vjaが1650以上の場合、吐出方向に乱れを生じ、連続紡糸が不安定となり好ましくない。
In carrying out the present invention, when Vf / Vja is 0.15 or less and when Vf / Vja is 0.50 or more, the drying behavior cannot catch up with the take-up speed, and continuous spinning becomes unstable, which is not preferable.
When Vja is 1200 or less, sufficient drying strain in the fiber axis direction is not formed, and the target elongation rate cannot be obtained. Further, when Vja is 1650 or more, the discharge direction is disturbed and the continuous spinning becomes unstable, which is not preferable.
一方、Vf/Vjbが0.15以下の場合、及びVf/Vjbが1.20以上の場合もジアセテート繊維と同様の問題が生じ、好ましくない。
また、Vjbが200以下の場合、原料の送液量が減少し、吐出量が不安定となり好ましくない。更に、Vjbが1650以上の場合、吐出方向に乱れを生じ、連続紡糸が不安定となり好ましくない。
On the other hand, when Vf / Vjb is 0.15 or less and when Vf / Vjb is 1.20 or more, problems similar to those of diacetate fiber occur, which is not preferable.
On the other hand, when Vjb is 200 or less, the feed amount of the raw material decreases, and the discharge amount becomes unstable, which is not preferable. Further, when Vjb is 1650 or more, the discharge direction is disturbed and the continuous spinning becomes unstable, which is not preferable.
また、Vfが300より小さい場合、生産性が低くなり、Vfが700を超える場合、2成分の交絡付与性が劣り、十分な異収縮特性を発揮できない。 Further, when Vf is smaller than 300, productivity is low, and when Vf exceeds 700, the confounding property of the two components is inferior, and sufficient different shrinkage characteristics cannot be exhibited.
本発明は、混繊糸を構成するジアセテート繊維とトリアセテート繊維はジアセテート繊維の伸長率が5%以上、且つ、トリアセテート繊維の収縮率が0%以上であることが好ましい。
ジアセテート繊維の伸長率が5%未満であると、従来知られた嵩高性やソフト感のままであり、消費者ニーズの多様化に合わせた、極度な嵩高性やソフト差の表現は困難である。
一方、トリアセテート繊維の収縮率が0%未満となる場合も極度な嵩高性やソフト差の表現は困難である。
In the present invention, it is preferable that the diacetate fiber and the triacetate fiber constituting the mixed yarn have a diacetate fiber elongation of 5% or more and a triacetate fiber shrinkage of 0% or more.
If the elongation rate of diacetate fiber is less than 5%, the conventional bulkiness and softness will remain as it is, and it will be difficult to express extreme bulkiness and softness to meet diversifying consumer needs. is there.
On the other hand, even when the shrinkage rate of the triacetate fiber is less than 0%, it is difficult to express extreme bulkiness and soft difference.
また、ジアセテート繊維とトリアセテート繊維の繊度比がジアセテート繊維/トリアセテート繊維<0.5であると、ジアセテート繊維の伸長特性が得られる混繊糸の風合いに寄与されにくくなり、ジアセテート繊維の単繊維繊度が6dtex以上であると風合いは硬くなり好ましくない。
本発明を実施するに当たってはセルローストリアセテートの紡糸原液とセルロースジアセテート紡糸原液を夫々別の紡糸口金より、両口金間に所定の距離を設け同時に紡糸する。紡糸に当たっては各紡糸錘の間隔を予め定めて設定する。各紡糸錘から吐出され乾式紡糸された糸条はエアー交絡し混繊糸となる。
Further, when the fineness ratio of diacetate fiber and triacetate fiber is diacetate fiber / triacetate fiber <0.5, it becomes difficult to contribute to the texture of the mixed yarn that gives the elongation characteristics of diacetate fiber. If the single fiber fineness is 6 dtex or more, the texture becomes hard, which is not preferable.
In carrying out the present invention, a cellulose triacetate spinning solution and a cellulose diacetate spinning solution are spun simultaneously from different spinnerets by providing a predetermined distance between the two spinnerets. In spinning, the interval between the spinning spindles is set in advance. The yarn discharged from each spinning spindle and dry-spun is air entangled into a mixed yarn.
本発明の混繊糸を含む織編物は、他の繊維と交織・交編または交撚等により複合しているが、これらの場合、本発明の混繊糸が20質量%以上含まれていることが好ましい。20質量%未満になると膨らみ感の効果が得られにくい。 The woven or knitted fabric containing the blended yarn of the present invention is compounded with other fibers by knitting, knitting or knitting, and in these cases, the blended yarn of the present invention is contained in an amount of 20% by mass or more. It is preferable. If it is less than 20% by mass, it is difficult to obtain the effect of swelling.
以下、実施例をあげて本発明を説明する。なお、各評価は以下の方法に従った。 Hereinafter, the present invention will be described with reference to examples. In addition, each evaluation followed the following method.
〔熱水収縮率〕
1dtexあたり1/27gの張力下で試長1mの10回捲き綛を準備し、1dtexあたり2/2.7gの荷重を負荷して初期綛長(L0)を測定する。前記綛を無荷重状態で120℃の熱水中に30分間浸漬した後、再び荷重をかけて測定綛長(L1)を測定し、次式より算出する。
熱水収縮率(%)=(L0−L1)/L0×100
〔強伸度の測定〕
JIS−L1013−8.5(引っ張り強さ及び伸び率)に準拠して求めた。測定は、強伸度測定器(オリエンテック社製、製品名:RTA−500)を用いて測定した。
〔嵩高性〕
嵩高性は、JIS−L1018法により測定した。
[Hot water shrinkage]
A ten-throw firewood having a test length of 1 m is prepared under a tension of 1/27 g per 1 dtex, a load of 2 / 2.7 g per 1 dtex is applied, and the initial length (L0) is measured. After immersing the heel in 120 ° C. hot water for 30 minutes in an unloaded state, the load is again applied to measure the measurement heel length (L1), which is calculated from the following equation.
Hot water shrinkage (%) = (L0−L1) / L0 × 100
(Measurement of strength and elongation)
It calculated | required based on JIS-L1013-8.5 (tensile strength and elongation rate). The measurement was performed using a strong elongation measuring device (product name: RTA-500, manufactured by Orientec Corp.).
[Bulky]
Bulkiness was measured by the JIS-L1018 method.
(実施例1〜8)
水酸基の97%が酢酸化されているセルローストリアセテートを塩化メチレン/メタノールの混合溶剤に溶解した紡糸原液と、水酸基の80.3%が酢酸化されているセルロースジアセテートを塩化メチレン/メタノールの混合溶剤に溶解した紡糸原液とを隣り合う紡糸錘の間隔を15cmとして、それぞれ下記表1及び表2記載の条件にて乾式紡糸を行い、引き続き糸条に対して垂直な方向から圧縮空気流を作用させるインターレース・ノズルを用いて、35個/mの交絡を与えて、セルローストリアセテート繊維とセルロースジアセテート繊維からなる混繊糸を得た。
得られた混繊糸を30ゲージで編成した8cm巾の筒編地とし、120℃で30分間の熱水処理をしたところ、編地は膨らみ感の強い風合いを有していた。
(Examples 1-8)
A spinning stock solution in which cellulose triacetate in which 97% of hydroxyl groups are acetated is dissolved in a mixed solvent of methylene chloride / methanol, and cellulose diacetate in which 80.3% of hydroxyl groups are acetated are mixed in a solvent mixture of methylene chloride / methanol. The spinning stock solution dissolved in the yarn is dry-spun under the conditions shown in Table 1 and Table 2 below, with the distance between adjacent spinning spindles being 15 cm, and then a compressed air flow is applied from a direction perpendicular to the yarn. Using an interlace nozzle, entanglement of 35 pieces / m was given to obtain a mixed yarn composed of cellulose triacetate fibers and cellulose diacetate fibers.
When the obtained blended yarn was formed into a tubular knitted fabric of 8 cm width knitted with 30 gauge and subjected to hot water treatment at 120 ° C. for 30 minutes, the knitted fabric had a texture with a strong feeling of swelling.
(比較例1)
実施例2と同様に、下記表1及び表2記載の比較例1に記した条件にて乾式紡糸を行い、糸条に対して垂直な方向から圧縮空気流を作用させるインターレース・ノズルを用いて、35個/mの交絡を与えて、40dtexのセルローストリアセテート繊維と40dtexのセルロースジアセテート繊維からなる混繊糸を得た。
得られた混繊糸を30ゲージで編成した8cm巾の筒編地とし、120℃の熱水処理をしたところ、編地は膨らみ感の弱い風合いのものであった。
(Comparative Example 1)
Similarly to Example 2, dry spinning was performed under the conditions described in Comparative Example 1 described in Table 1 and Table 2 below, and an interlace nozzle was used to apply a compressed air flow from a direction perpendicular to the yarn. 35 / m was entangled to obtain a mixed yarn composed of 40 dtex cellulose triacetate fiber and 40 dtex cellulose diacetate fiber.
When the obtained mixed yarn was formed into a tubular knitted fabric of 8 cm width knitted with 30 gauge and subjected to hot water treatment at 120 ° C., the knitted fabric had a texture with a weak feeling of swelling.
(比較例2)
実施例1〜8と同様に、下記表1及び表2記載の比較例3に記した条件にて乾式紡糸を行い、エアー交絡にて絡みを与えて、80dtexのセルローストリアセテート繊維と25dtexのセルロースジアセテート繊維からなる混繊糸を得た。
得られた混繊糸を筒編とし、120℃の熱水処理をしたところ、編地は膨らみ感の弱い風合いのものであった。
(Comparative Example 2)
As in Examples 1 to 8, dry spinning was performed under the conditions described in Comparative Example 3 described in Tables 1 and 2 below, and entangled by air entanglement, and 80 dtex cellulose triacetate fiber and 25 dtex cellulose dice. A mixed yarn made of acetate fibers was obtained.
When the obtained mixed yarn was made into a tubular knitting and subjected to hot water treatment at 120 ° C., the knitted fabric had a texture with a weak feeling of swelling.
(実施例9)
実施例2で得られたセルロースアセテート混繊糸と、33dtex12fで熱水処理時の収縮差により自己捲縮発現性を有するポリエステル繊維とをエアー混繊し、113dtex35fのフィラメント混繊糸を製造、平織物(経:174本/吋、緯:97本/吋)を作成し、染色後、170℃で1分の乾熱処理を実施した。得られた織物(経:190本/吋、緯:98本/吋)は嵩高性に優れ、膨らみ感のあるソフトな風合を有していた。この織物の嵩高性は、3.6cm3 /gであった。
Example 9
The cellulose acetate mixed yarn obtained in Example 2 and the polyester fiber having the self-crimping expression due to the difference in shrinkage at the time of hydrothermal treatment at 33 dtex 12f were air mixed to produce a 113 dtex 35f filament mixed yarn. A woven fabric (warp: 174 / 吋, weft: 97 / 吋) was prepared, and after dyeing, dry heat treatment was performed at 170 ° C. for 1 minute. The obtained woven fabric (warp: 190 / pile, weft: 98 / pile) was excellent in bulkiness and had a soft texture with a feeling of swelling. The bulkiness of this fabric was 3.6 cm 3 / g.
Claims (1)
(1)0.15<Vf/Vja<0.50、且つ、1200<Vja<1650
(2)0.15<Vf/Vjb<1.20、且つ、200<Vjb<1650
(3)300≦Vf≦700
式中、Vfは紡出時の引き取り速度(m/分)、Vjaは、ジアセテート繊維の紡糸原液の紡糸ノズルからの吐出線速度(m/分)、Vjbは、トリアセテート繊維の紡糸原液の紡糸ノズルからの吐出線速度(m/分)を示す。 In the manufacturing method of the cellulose acetate mixed yarn which spins and mixes a diacetate fiber and a triacetate fiber simultaneously, the manufacturing method satisfy | fills following (1)-(3).
(1) 0.15 <Vf / Vja <0.50 and 1200 <Vja <1650
(2) 0.15 <Vf / Vjb <1.20 and 200 <Vjb <1650
(3) 300 ≦ Vf ≦ 700
In the formula, Vf is the take-up speed during spinning (m / min), Vja is the discharge linear speed from the spinning nozzle of the spinning solution of diacetate fiber (m / min), and Vjb is the spinning of the spinning solution of triacetate fiber. The discharge linear velocity (m / min) from the nozzle is shown.
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JPS6350515A (en) * | 1986-08-13 | 1988-03-03 | Mitsubishi Rayon Co Ltd | Production of acetate fiber |
JPH09268424A (en) * | 1996-03-29 | 1997-10-14 | Mitsubishi Rayon Co Ltd | New cellulose ester solution and production of cellulose ester using the same |
JP3255873B2 (en) * | 1997-04-18 | 2002-02-12 | 三菱レイヨン株式会社 | Spinneret for cellulose acetate fiber and method for producing the fiber |
JP4217350B2 (en) * | 1999-07-13 | 2009-01-28 | 三菱レイヨン株式会社 | Method for producing novel cellulose acetate thick yarn |
JP3545276B2 (en) * | 1999-10-06 | 2004-07-21 | 三菱レイヨン株式会社 | Spontaneously extensible cellulose acetate fiber and method for producing the same |
JP2002105784A (en) * | 2000-09-28 | 2002-04-10 | Mitsubishi Rayon Co Ltd | Cellulose acetate multifilament yarn with heterofineness and method for producing the same and wove/knitted fabric made therefrom |
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