JPH09228154A - Production of polyester conjugate fiber with latent crimp tendency - Google Patents
Production of polyester conjugate fiber with latent crimp tendencyInfo
- Publication number
- JPH09228154A JPH09228154A JP6926896A JP6926896A JPH09228154A JP H09228154 A JPH09228154 A JP H09228154A JP 6926896 A JP6926896 A JP 6926896A JP 6926896 A JP6926896 A JP 6926896A JP H09228154 A JPH09228154 A JP H09228154A
- Authority
- JP
- Japan
- Prior art keywords
- polyester
- conjugate fiber
- fiber
- heat treatment
- elongation
- 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 60
- 229920000728 polyester Polymers 0.000 title claims abstract description 34
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 238000010438 heat treatment Methods 0.000 claims abstract description 31
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000002131 composite material Substances 0.000 claims description 17
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 5
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 claims description 2
- 239000004745 nonwoven fabric Substances 0.000 abstract description 12
- 239000004744 fabric Substances 0.000 abstract description 7
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 abstract description 2
- WPSWDCBWMRJJED-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol;oxirane Chemical compound C1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 WPSWDCBWMRJJED-UHFFFAOYSA-N 0.000 abstract 1
- 238000009987 spinning Methods 0.000 description 14
- 238000000034 method Methods 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 229920000139 polyethylene terephthalate Polymers 0.000 description 9
- 239000005020 polyethylene terephthalate Substances 0.000 description 9
- 238000002788 crimping Methods 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- -1 polyethylene terephthalate Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000002074 melt spinning Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- XGIAHMUOCFHQTI-UHFFFAOYSA-N Cl.Cl.Cl.Cl.CC Chemical compound Cl.Cl.Cl.Cl.CC XGIAHMUOCFHQTI-UHFFFAOYSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Multicomponent Fibers (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、熱処理を施すとス
パイラル捲縮を発現し、良好な伸縮性能を有するものと
なる潜在捲縮性ポリエステル複合繊維の製造方法に関す
るものである。TECHNICAL FIELD The present invention relates to a method for producing a latently crimpable polyester composite fiber which exhibits spiral crimps when heat-treated and has good stretchability.
【0002】[0002]
【従来の技術】ポリエステル繊維は、衣料用、産業資材
用等種々の用途に使用されているが、中でもスポーツ衣
料用途においては、伸縮性の高い繊維が要望されてい
る。伸縮性の高い繊維を得るために、従来より熱収縮特
性の異なるポリマーをサイドバイサイドまたは偏心芯鞘
構造に複合した、潜在捲縮性複合繊維が数多く提案され
ている。2. Description of the Related Art Polyester fibers are used for various purposes such as clothing and industrial materials. Above all, in sports clothing applications, highly stretchable fibers are desired. In order to obtain highly stretchable fibers, a large number of latent crimpable conjugate fibers have been proposed in which polymers having different heat shrinkage properties are compounded in a side-by-side or eccentric core-sheath structure.
【0003】例えば、特公平4−5769号公報、特公平3
−10737 号には、5-ナトリウムスルホイソフタル酸成分
を共重合したポリエチレンテレフタレート系共重合ポリ
エステルとポリエチレンテレフタレートとの複合繊維が
開示されている。また、特開平7− 54216号公報にはイ
ソフタル酸とビスフェノールAのエチレンオキシド付加
体(BAEO)とを共重合したポリエステルとポリエチ
レンテレフタレートとの複合繊維が開示されている。For example, Japanese Patent Publication No. 4-5769 and Japanese Patent Publication 3
No. -10737 discloses a composite fiber of polyethylene terephthalate and a polyethylene terephthalate-based copolyester obtained by copolymerizing a 5-sodium sulfoisophthalic acid component. Further, Japanese Patent Application Laid-Open No. 7-54216 discloses a composite fiber of polyester and polyethylene terephthalate obtained by copolymerizing isophthalic acid and an ethylene oxide adduct (BAEO) of bisphenol A.
【0004】これらの複合繊維は一般的な製糸方法で得
られるため、伸度が30〜50%前後であり、強度も低かっ
た。このため、この複合繊維を製編織して得られた布帛
は、スポーツ衣料用途として用いると、スライディング
等を行い、摩擦力が加わった際に容易に破れるという問
題があった。また、伸度が高く、強度が低いために、こ
れらの複合繊維は、紡績工程において工程を高速化する
ことができないという問題もあった。Since these conjugate fibers can be obtained by a general yarn making method, the elongation is about 30 to 50% and the strength is low. Therefore, the fabric obtained by weaving and knitting this composite fiber has a problem that when it is used for sports clothing, it is easily broken when subjected to sliding force and frictional force. Further, since the elongation is high and the strength is low, there is a problem that these conjugate fibers cannot speed up the spinning process.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上記のよう
な問題点を解決し、短繊維にすれば、高速での紡績が可
能であり、かつ摩擦に強い布帛や不織布を得ることがで
きる、低伸度、高強度の潜在捲縮性ポリエステル複合繊
維を製造する方法を提供することを技術的な課題とする
ものである。SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems, and if short fibers are used, it is possible to obtain a cloth or a non-woven fabric which can be spun at high speed and is resistant to friction. It is a technical object to provide a method for producing a latently crimpable polyester conjugate fiber having low elongation and high strength.
【0006】[0006]
【課題を解決するための手段】本発明者らは、このよう
な課題を解決するために鋭意検討の結果、本発明に到達
した。すなわち、本発明は、エチレンテレフタレートを
主体とするポリエステル(A)とイソフタル酸1〜4.5
モル%とビスフェノールAのエチレンオキシド付加物2
〜7モル%とを共重合したポリエステル(B)とが偏心
的に接合しており、170 ℃における自由収縮熱処理での
収縮率が15%以下であり、かつ、170 ℃での弛緩熱処理
により発現するスパイラル捲縮数が50個/25mm以上、
伸度が25%以下、強度が6.5 g/d以上である複合繊維
を製造するに際し、延伸を二段階で行い、トータル延伸
倍率の70〜95%の倍率で一段目の延伸を、続いて、加熱
蒸気処理器内を通過させながら、加熱蒸気温度130 〜17
0 ℃、滞留時間0.5 秒以上として二段目の延伸を行うこ
とを特徴とする潜在捲縮性ポリエステル複合繊維の製造
方法を要旨とするものである。The present inventors have arrived at the present invention as a result of intensive studies to solve such problems. That is, the present invention relates to a polyester (A) mainly composed of ethylene terephthalate and isophthalic acid 1 to 4.5.
Ethylene oxide adduct of mol% and bisphenol A 2
Polyester (B) copolymerized with ~ 7 mol% is eccentrically bonded, the shrinkage ratio at free heat treatment at 170 ° C is 15% or less, and the heat treatment at 170 ° C causes relaxation. The number of spiral crimps is 50/25 mm or more,
When producing a composite fiber having an elongation of 25% or less and a strength of 6.5 g / d or more, the stretching is performed in two stages, and the first stage is stretched at a draw ratio of 70 to 95% of the total draw ratio. While passing through the heating steam processor, the heating steam temperature 130 to 17
A gist of the present invention is a method for producing a latently crimpable polyester conjugate fiber, which comprises performing a second stage drawing at 0 ° C for a residence time of 0.5 seconds or more.
【0007】[0007]
【発明の実施の形態】以下、本発明について詳細に説明
する。本発明で製造される複合繊維は、ポリエステル
(A)とポリエステル(B)とを偏心的に接合したもの
であり、ポリエステル(A)としては、ポリエチレンテ
レフタレート(PET)が好ましく用いられるが、本発
明の効果を損なわない範囲内であれば、PETにイソフ
タル酸(IPA)、1,4-ブタンジオール、1,6-ヘキサン
ジオール、ジエチレングリコール、ポリエチレングリコ
ール等の成分を共重合したものでもよい。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below. The conjugate fiber produced by the present invention is one in which polyester (A) and polyester (B) are eccentrically joined, and polyethylene terephthalate (PET) is preferably used as polyester (A). If the effect is not impaired, PET may be copolymerized with components such as isophthalic acid (IPA), 1,4-butanediol, 1,6-hexanediol, diethylene glycol and polyethylene glycol.
【0008】一方、ポリエステル(B)としては、エチ
レンテレフタレート単位を主体とし、IPAを1〜4.5
モル%とBAEOを2〜7モル%を共重合したものとす
る必要がある。IPAの共重合割合が1モル%未満であ
ると、得られる複合繊維は潜在捲縮性能が不十分とな
り、4.5 モル%を超えると、ポリマーの融点が低下し、
ポリエステル(A)と(B)とが偏心的に接合した複合
繊維を得ることができなくなる。On the other hand, as the polyester (B), ethylene terephthalate units are mainly used, and IPA is 1 to 4.5.
It is necessary to copolymerize 2% to 7% by mol of BAEO with mol%. If the copolymerization ratio of IPA is less than 1 mol%, the resulting composite fiber will have insufficient latent crimp performance, and if it exceeds 4.5 mol%, the melting point of the polymer will decrease.
It becomes impossible to obtain a composite fiber in which the polyesters (A) and (B) are eccentrically joined.
【0009】また、BAEOの共重合量が2モル%未満
であると、得られる複合繊維は潜在捲縮性能が不十分と
なり、この複合繊維を不織布や紡績糸にした場合、伸長
率や伸長回復率が小さく、伸縮性能が劣るものとなる。
一方、7モル%を超えると、ポリマーの融点が低下した
り、得られる繊維の強度が低下する。BAEOは、ビス
フェノールA1モルに対して、エチレンオキシドを2〜
10モル付加したものが好ましく、さらに好ましくは2〜
5モル付加したものである。When the amount of BAEO copolymerized is less than 2 mol%, the resulting composite fiber has insufficient latent crimp performance, and when the composite fiber is used as a nonwoven fabric or spun yarn, the elongation rate and elongation recovery are obtained. The rate is small and the expansion / contraction performance is poor.
On the other hand, when it exceeds 7 mol%, the melting point of the polymer is lowered and the strength of the obtained fiber is lowered. BAEO contains 2 moles of ethylene oxide per 1 mole of bisphenol A.
It is preferable to add 10 mol, more preferably 2 to
5 moles are added.
【0010】本発明において、複合繊維を構成するポリ
エステル(A)と(B)の極限粘度は特に限定されるも
のではないが、溶融紡糸を円滑に行う点から、ポリエス
テル(A)は0.50〜0.70、ポリエステル(B)は0.55〜
0.75のものが好ましい。そして、紡糸安定性に優れ、か
つ後工程で十分に捲縮が発現する複合繊維とするために
は、2種のポリマーの極限粘度差を0.25以下にすること
が好ましい。粘度差が0.25より大きくなると口金直下の
糸条の曲がりが大きくなり、紡糸が不安定になりやす
い。In the present invention, the intrinsic viscosities of the polyesters (A) and (B) constituting the conjugate fiber are not particularly limited, but from the viewpoint of smooth melt spinning, the polyester (A) is 0.50 to 0.70. , Polyester (B) is 0.55 ~
0.75 is preferable. Then, in order to obtain a conjugate fiber which is excellent in spinning stability and in which crimps are sufficiently expressed in the subsequent step, it is preferable that the intrinsic viscosity difference between the two kinds of polymers is 0.25 or less. If the difference in viscosity is more than 0.25, the bending of the yarn just below the spinneret becomes large, and the spinning tends to become unstable.
【0011】そして、ポリエステル(A)と(B)とが
偏心的に接合した複合繊維としては、サイドバイサイド
や偏心芯鞘構造のもの等が挙げられ、断面形状は、円形
断面、偏平、六葉、三角断面等の異形あるいは中空断面
等のものが挙げられる。The composite fibers in which the polyesters (A) and (B) are joined eccentrically include those having a side-by-side structure or an eccentric core-sheath structure. Examples include irregular shapes such as a triangular cross section or hollow cross sections.
【0012】次に、本発明の前記したようなポリエステ
ル(A)と(B)とからなる複合繊維の製造方法につい
て説明する。まず、ポリエステル(A)、(B)を用い
て、通常の複合紡糸装置により、横断面形状がサイドバ
イサイドや偏心芯鞘構造の複合繊維を紡糸する。なお、
紡糸に際し、ポリマー中に安定剤、蛍光剤、顔料、強化
剤等を含有させてもよい。そして、得られた未延伸糸
を、TDRの70〜95%の倍率で一段目の延伸を行い、続
いて、加熱蒸気処理器内を通過させながら、加熱蒸気温
度130 〜170 ℃、滞留時間0.5 秒以上として、二段目の
延伸を行うことが必要である。Next, a method for producing the conjugate fiber of the present invention, which comprises the polyesters (A) and (B) as described above, will be described. First, the polyesters (A) and (B) are used to spin a conjugate fiber having a side-by-side or eccentric core-sheath structure in a cross-sectional shape by an ordinary conjugate spinning device. In addition,
During spinning, the polymer may contain stabilizers, fluorescent agents, pigments, reinforcing agents and the like. Then, the obtained undrawn yarn is drawn in the first stage at a draw ratio of 70 to 95% of TDR, and subsequently, while passing through the heating steam processor, the heating steam temperature is 130 to 170 ° C. and the residence time is 0.5. It is necessary to perform the second stage stretching for not less than 2 seconds.
【0013】一段目の延伸でTDRの95%を超えた倍率
で延伸すると、一段目の延伸倍率が高過ぎるため、糸切
れが発生して操業性が著しく悪化し、得られる複合繊維
は物性が低下したものとなる。また、TDRの70%未満
の倍率で一段目の延伸を行うと、二段目の延伸倍率が高
くなり過ぎるため、加熱蒸気処理の段階で単糸間で融着
が発生する。When the first stage drawing is carried out at a draw ratio of more than 95% of TDR, the first step draw ratio is too high, so that yarn breakage occurs and the operability is remarkably deteriorated. It will be lowered. If the first stage is drawn at a draw ratio of less than 70% of TDR, the draw ratio of the second stage becomes too high, so that fusion occurs between the single yarns in the stage of heating steam treatment.
【0014】上記のような延伸において、TDRは3.7
倍以上とすることが好ましく、より好ましくは4.0 倍以
上である。一段目の延伸の延伸倍率は、好ましくは2.6
〜3.8 倍であり、二段目の延伸の延伸倍率は好ましく
は、1.05〜1.5 倍である。In the above stretching, TDR is 3.7.
It is preferably double or more, and more preferably 4.0 or more. The stretching ratio of the first stage stretching is preferably 2.6
The stretch ratio in the second stage stretching is preferably 1.05 to 1.5 times.
【0015】二段目の延伸は加熱蒸気処理器により蒸気
で加熱しながら延伸を行うが、処理器より噴出させる加
熱蒸気の温度を130 〜170 ℃とすることが必要であり、
さらに好ましくは140 〜150 ℃とする。そして、加熱蒸
気処理器内に糸条を滞留させて加熱を行う時間を0.5 秒
以上とする必要がある。加熱蒸気処理器の蒸気の温度
が、130 ℃未満では糸条が均一に十分に加熱されないた
めに、得られる繊維は伸度が高く、強度の小さいものと
なる。 170℃を超えると繊維同士が融着を起こしたり、
糸切れが発生する。The second stage drawing is carried out while heating with steam in a heating steam processor, but it is necessary to set the temperature of the heated steam ejected from the processor to 130 to 170 ° C.
More preferably, the temperature is 140 to 150 ° C. Then, it is necessary to set the time for heating the yarn by allowing the yarn to stay in the heating steam processor to be 0.5 seconds or more. If the temperature of the steam in the heating steam processor is less than 130 ° C., the yarn is not uniformly and sufficiently heated, so that the obtained fiber has high elongation and low strength. If the temperature exceeds 170 ° C, the fibers will fuse together,
Thread breaks occur.
【0016】加熱蒸気処理器内に糸条を滞留させて熱処
理する時間は0.5 秒以上とすることが必要で、好ましく
は1〜3秒とする。滞留時間が0.5 秒未満では、糸条へ
の熱伝達が不十分となり、十分な熱処理ができない。滞
留時間の上限は特に限定されるものではないが、3秒程
度である。The time required for heat treatment by allowing the yarn to stay in the heated steam processor must be 0.5 seconds or more, preferably 1 to 3 seconds. If the residence time is less than 0.5 seconds, heat transfer to the yarn will be insufficient and sufficient heat treatment will not be possible. The upper limit of the residence time is not particularly limited, but is about 3 seconds.
【0017】本発明の製造方法で得られた複合繊維を、
紡績糸や不織布を得るために短繊維として用いる場合、
紡績工程やカード工程における通過性をよくするため
に、二段目の延伸を行った後、8〜18個/25mm、さら
に10〜16個/25mmの機械捲縮を付与することが好まし
い。機械捲縮の数が8個/25mm未満であると、上記の
ような工程における通過性を向上させる効果が少なく、
18個/25mmを超えると、機械捲縮を付与するために時
間やコストがかかり好ましくない。機械捲縮を付与する
方法は特に限定されるものではないが、押込み式捲縮装
置等を用いる方法が挙げられる。The composite fiber obtained by the production method of the present invention is
When used as short fibers to obtain spun yarn or nonwoven fabric,
In order to improve the passability in the spinning process and the card process, it is preferable to apply a mechanical crimp of 8 to 18 pieces / 25 mm, and further 10 to 16 pieces / 25 mm after the second stage drawing. When the number of mechanical crimps is less than 8 pieces / 25 mm, the effect of improving the passability in the above steps is small,
When it exceeds 18 pieces / 25 mm, it takes time and cost to apply the mechanical crimp, which is not preferable. The method for applying the mechanical crimp is not particularly limited, and examples thereof include a method using a press-type crimping device.
【0018】そして、このような延伸、熱処理を行うこ
とにより、強度が6.5 g/d以上、伸度が25%以下であ
り、170 ℃における自由収縮熱処理での収縮率が15%以
下であり、かつ170 ℃での弛緩熱処理により発現するス
パイラル捲縮数が50個/25mm以上である潜在捲縮性の
複合繊維を得ることができる。By carrying out such stretching and heat treatment, the strength is 6.5 g / d or more, the elongation is 25% or less, and the shrinkage ratio in the free shrink heat treatment at 170 ° C. is 15% or less. Moreover, a latent crimpable conjugate fiber having a number of spiral crimps of 50/25 mm or more developed by relaxation heat treatment at 170 ° C. can be obtained.
【0019】強度が6.5 g/d未満で、伸度が25%を超
えると、このような複合繊維は、紡績工程において工程
を高速化することができず、また、摩擦力に強い、良好
な捲縮性能を有する布帛とすることができない。170 ℃
における自由収縮熱処理での収縮率が15%を超えると、
この複合繊維を用いて得られる布帛は、風合の硬いもの
となる。複合繊維のスパイラル捲縮数が50個/25mm未
満であると、得られる布帛は伸縮性に劣るものとなる。When the strength is less than 6.5 g / d and the elongation is more than 25%, such a composite fiber cannot be speeded up in the spinning process and is strong in frictional force. A cloth having crimp performance cannot be obtained. 170 ° C
When the shrinkage rate in free shrink heat treatment in
The cloth obtained by using this composite fiber has a hard texture. When the number of spiral crimps of the composite fiber is less than 50/25 mm, the obtained fabric has poor stretchability.
【0020】本発明においては、未延伸糸の繊度は特に
限定されるものではなく、長繊維を得る場合には、30〜
200 デニールの糸条とし、紡績糸や不織布用の短繊維を
得るためには、1〜100 万デニールの糸束に集束してか
ら延伸を行うことが好ましい。そして、一段目の延伸は
乾式、湿式のいずれでもよいが、温水浴等を用いた湿式
延伸を行うと、延伸点が固定されやすいので好ましい。In the present invention, the fineness of the undrawn yarn is not particularly limited, and in the case of obtaining long fibers, the fineness is 30 to
In order to obtain a 200 denier yarn and to obtain spun yarn and short fibers for a nonwoven fabric, it is preferable to bundle the yarn into a yarn bundle of 1 to 1 million denier and then draw. The first-stage stretching may be dry or wet, but wet stretching using a hot water bath or the like is preferable because the stretching point is easily fixed.
【0021】また、本発明の方法で得られた複合繊維
は、紡績工程において紡績糸とした場合は、染色時の熱
処理によってスパイラル捲縮が発現され、不織布を作成
する場合には、カードウエブを熱処理する際にスパイラ
ル捲縮が発現される。Further, when the conjugate fiber obtained by the method of the present invention is used as a spun yarn in the spinning process, spiral crimp is developed by heat treatment during dyeing, and when a nonwoven fabric is produced, a card web is used. Spiral crimps develop during heat treatment.
【0022】次に、本発明を図面を用いて説明する。図
1は、本発明の一実施態様を示す概略工程図である。未
延伸糸糸束Yをフィードローラ1と、第一ドローローラ
2との間で温水浴6を通過させながら、一段目の延伸を
施す。続いて、未延伸糸糸束Yを第一ドローローラ2と
第二ドローローラ3との間で加熱蒸気処理器5内を通過
させながら、二段目の延伸を行う。そして、延伸後の糸
束を引取ローラ4で引き取る。このとき、本発明の効果
を損なわない範囲であれば、引取ローラ4を120 〜170
℃程度に加熱し、第二ドローローラ3との間で弛緩熱処
理を施してもよい。また、機械捲縮を付与する場合は、
引取ローラ4で引き取った後、続いて押込み式捲縮装置
等で機械捲縮を付与する。Next, the present invention will be described with reference to the drawings. FIG. 1 is a schematic process diagram showing an embodiment of the present invention. While passing the undrawn yarn yarn bundle Y through the hot water bath 6 between the feed roller 1 and the first draw roller 2, the first stage drawing is performed. Subsequently, the undrawn yarn yarn bundle Y is drawn between the first draw roller 2 and the second draw roller 3 while passing through the inside of the heated steam processor 5, and the second stage drawing is performed. Then, the drawn yarn bundle is taken up by the take-up roller 4. At this time, if the take-up roller 4 is in the range of 120 to 170 as long as the effect of the present invention is not impaired.
The relaxation heat treatment may be performed with the second draw roller 3 by heating to about ° C. Also, when mechanical crimping is applied,
After being taken up by the take-up roller 4, mechanical crimping is applied by a push-type crimping device or the like.
【0023】[0023]
【実施例】次に、本発明を実施例を用いて具体的に説明
する。なお、実施例中の各種の特性値の測定法は、次の
とおりである。 (1) 極限粘度〔η〕 フェノールと四塩化エタンとの等重量混合物を溶媒と
し、温度20℃で測定した。 (2) 繊度 JIS L−1015 7-5-1Aの方法で測定した。 (3) 強度、伸度 JIS L−1015 7-7 の方法で測定した。 (4) 捲縮数(スパイラル捲縮数) 得られた繊維を170 ℃で5分間、自由に収縮しうる状態
(無荷重)で熱処理した後、JIS L−1015 7-21-1
の方法により、繊維に発現したスパイラル捲縮数を測定
した。 (5) 自由収縮率 JIS L−1015 7-15に準じ、1デニール当たり300
mgの荷重をかけて測定した。 (6) 精紡糸強力 40番手の精紡糸を得、得られた精紡糸を40cmにカット
し、引っ張り試験機で速度20cm/分で引っ張り、強力
を測定した。 (7) 不織布強力 得られた繊維を目付50g/m2 のカードウエブにして、
170 ℃で1分処理して不織布を得た。この不織布を緯25
mm、経 150mmにカットし、JIS L−1096の方法
で測定した。Next, the present invention will be specifically described with reference to examples. In addition, the measuring method of various characteristic values in an Example is as follows. (1) Intrinsic viscosity [η] It was measured at a temperature of 20 ° C using an equal weight mixture of phenol and ethane tetrachloride as a solvent. (2) Fineness Measured by the method of JIS L-1005 7-5-1A. (3) Strength and elongation Measured by the method of JIS L-1015 7-7. (4) Number of crimps (number of spiral crimps) After heat-treating the obtained fibers at 170 ° C. for 5 minutes in a freely shrinkable state (no load), JIS L-1015 7-21-1
The number of spiral crimps developed in the fiber was measured by the method described in 1. (5) Free shrinkage: According to JIS L-1015 7-15, 300 per 1 denier
It was measured by applying a load of mg. (6) Spun spinning strength A 40-spun spun yarn was obtained, the resulting spun yarn was cut into 40 cm, and the tenacity was measured with a tensile tester at a speed of 20 cm / min to measure the tenacity. (7) Nonwoven fabric strength The obtained fiber is made into a card web having a basis weight of 50 g / m 2 ,
A nonwoven fabric was obtained by treating at 170 ° C. for 1 minute. Weft 25
mm, length 150 mm, and measured by the method of JIS L-1096.
【0024】実施例1 ポリエステル(A)として極限粘度0.67のPET、ポリ
エステル(B)として、PETにIPAを4モル%とB
AEO(エチレンオキシド2モル付加物)を3モル%共
重合した極限粘度0.70の共重合PETを用い、ポリエス
テル(A)、(B)のチップをそれぞれ常法により減圧
乾燥した後、通常の複合紡糸装置を使用して溶融紡糸を
行った。このとき、直径0.45mmの丸断面の細孔344 個
を有し、2種類のポリエステルがサイドバイサイドに複
合(重量比1:1)する紡糸口金を用いて、紡糸温度29
0 ℃、総吐出量230 g/分で複合紡糸した。紡出糸条を
空気で冷却した後、1000m/分の速度で引き取って未延
伸糸を得た。次に、得られた糸条を集束し、10万デニー
ルのトウにして、図1に示す延伸装置を用いて二段延伸
を行った。まず、フィードローラの温度を70℃、温水浴
の温度を60℃、フィードローラと第一ドローローラとの
間で一段目の延伸を行い、第一ドローローラの温度を85
℃とし、加熱蒸気処理器で145 ℃の加熱蒸気中を1.5秒
間滞留させ、第一ドローローラと第二ドローローラ(60
℃)との間で二段目の延伸を行った。続いて、引取ロー
ラの温度を170 ℃として引き取り、続いて押込み式捲縮
装置で12個/25mmの機械捲縮を付与し、51mmにカッ
トして短繊維を得た。このとき、TDRは4.02倍、一段
目の延伸倍率3.72倍(TDRの92.6%) 、二段目の延伸
倍率1.08倍であった。得られた繊維の物性、この繊維を
スピンドル回転数15000rpmで精紡して得られた精紡糸の
強力及びこの繊維より得られた不織布の強力を表2に示
す。Example 1 As polyester (A), PET having an intrinsic viscosity of 0.67, and as polyester (B), 4 mol% of IPA and B were added to PET.
Using a copolymerized PET having an intrinsic viscosity of 0.70 in which 3 mol% of AEO (ethylene oxide 2 mol adduct) was copolymerized, polyester (A) and (B) chips were dried under reduced pressure by a conventional method, and then an ordinary composite spinning device was used. Was used for melt spinning. At this time, using a spinneret having 344 pores with a round cross section of 0.45 mm in diameter and having two types of polyester compounded side by side (weight ratio 1: 1), a spinning temperature of 29
Composite spinning was performed at 0 ° C. and a total discharge rate of 230 g / min. The spun yarn was cooled with air and then taken off at a speed of 1000 m / min to obtain an undrawn yarn. Next, the obtained yarns were bundled into a tow of 100,000 denier, and two-stage drawing was performed using the drawing device shown in FIG. First, the temperature of the feed roller is 70 ° C, the temperature of the hot water bath is 60 ° C, the first stage stretching is performed between the feed roller and the first draw roller, and the temperature of the first draw roller is 85 ° C.
℃ and heated steam at 145 ℃ for 1.5 seconds in the steam processor, and the first draw roller and the second draw roller (60
C.) and the second drawing was performed. Subsequently, the temperature of the take-up roller was taken out at 170 ° C., and then 12 crimps / 25 mm of mechanical crimps were applied by a press-type crimping device and cut into 51 mm to obtain short fibers. At this time, TDR was 4.02 times, the first stage draw ratio was 3.72 times (92.6% of TDR), and the second stage draw ratio was 1.08 times. Table 2 shows the physical properties of the obtained fiber, the tenacity of the spun yarn obtained by spinning the fiber at a spindle speed of 15,000 rpm, and the tenacity of the non-woven fabric obtained from the fiber.
【0025】実施例2〜3、比較例1〜8 ポリエステル(B)のIPA、BAEOの共重合モル
比、TDR、一段目の延伸倍率(TDRを100 としたと
きの割合) 、二段目の延伸倍率、加熱蒸気処理器の加熱
蒸気の温度及び滞留時間を表1に示すように種々変更し
た以外は実施例1と同様にして、潜在捲縮性の複合繊維
を製造した。得られた繊維の物性、この繊維をスピンド
ル回転数15000rpm(比較例2は13500rpm、比較例3は14
000rpm)で精紡して得られた精紡糸の強力及びこの繊維
より得られた不織布の強力を表2に示す。Examples 2 to 3 and Comparative Examples 1 to 8 Copolymer molar ratio of polyester (B) of IPA and BAEO, TDR, draw ratio of the first step (ratio when TDR is 100), second step. A latent crimpable conjugate fiber was produced in the same manner as in Example 1 except that the draw ratio, the temperature of the heated steam in the heated steam processor and the residence time were variously changed as shown in Table 1. The physical properties of the obtained fiber, the number of revolutions of the fiber was 15,000 rpm (13500 rpm for Comparative Example 2 and 14 for Comparative Example 3).
Table 2 shows the tenacity of the spun yarn obtained by spinning at 000 rpm) and the tenacity of the non-woven fabric obtained from this fiber.
【0026】[0026]
【表1】 [Table 1]
【0027】[0027]
【表2】 [Table 2]
【0028】表2から明らかなように、実施例1〜3で
得られた繊維は優れた捲縮発現性能を有し、かつ、低伸
度、高強力であり、この繊維より得られた精紡糸及び不
織布ともに強力の高いものであった。一方、比較例1
は、ポリエステル(B)がBAEOの共重合されていな
いものであったために、比較例2は、ポリエステル
(B)がIPAの共重合されていないものであったため
に、得られた繊維は強伸度特性、捲縮発現性能ともに劣
るものであった。また、比較例3は、ポリエステル
(B)のBAEOとIPAの共重合量が多過ぎるため
に、得られた繊維は伸度が大きく、強度も低いものであ
った。比較例4は、加熱蒸気処理器の温度が低過ぎたた
めに、比較例6は、加熱蒸気処理器での滞留時間が短過
ぎたために、十分に熱処理することができず、得られた
繊維は伸度が大きく、強度も低いものであった。また、
比較例5は、加熱蒸気処理器の温度が高過ぎたために、
比較例8では二段目の延伸倍率が高過ぎたために、加熱
蒸気処理器で二段目の延伸を行う際、単糸の融着が発生
し、延伸糸を得ることができなかった。比較例7は、一
段目の延伸倍率が高過ぎたために、一段目の延伸工程で
糸切れによる糸束のローラ巻き付きが発生し、延伸糸を
得ることができなかった。As is clear from Table 2, the fibers obtained in Examples 1 to 3 have excellent crimp-developing performance, low elongation and high tenacity. Both the spun yarn and the non-woven fabric had high strength. On the other hand, Comparative Example 1
In Comparative Example 2, the polyester (B) was not copolymerized with BAEO, and the polyester (B) was not copolymerized with IPA. Both the degree property and the crimp development performance were inferior. Further, in Comparative Example 3, since the copolymerization amount of BAEO and IPA of the polyester (B) was too large, the obtained fiber had high elongation and low strength. In Comparative Example 4, the temperature of the heating steam processor was too low, and in Comparative Example 6, the residence time in the heating steam processor was too short, so that heat treatment could not be sufficiently performed, and the obtained fiber was The elongation was high and the strength was low. Also,
In Comparative Example 5, since the temperature of the heating steam processor was too high,
In Comparative Example 8, since the draw ratio of the second step was too high, when the second step of drawing was performed with the heating steam treatment device, fusion of the single yarn occurred and the drawn yarn could not be obtained. In Comparative Example 7, since the draw ratio of the first step was too high, roller winding of the yarn bundle occurred due to yarn breakage in the first step, and a drawn yarn could not be obtained.
【0029】[0029]
【発明の効果】本発明によれば、短繊維にすれば、高速
での紡績が可能であり、熱処理によってスパイラル捲縮
を発現し、良好な伸縮性能を有する摩擦に強い布帛や不
織布を得ることができる、潜在捲縮性ポリエステル複合
繊維を容易に製造することが可能となる。EFFECTS OF THE INVENTION According to the present invention, short fibers can be spun at a high speed, a spiral crimp is developed by heat treatment, and a friction-resistant cloth or non-woven fabric having good stretchability is obtained. It is possible to easily produce the latently crimpable polyester conjugate fiber.
【図1】本発明の一実施態様を示す概略工程図である。FIG. 1 is a schematic process diagram showing an embodiment of the present invention.
1 フィードローラ 2 第一ドローローラ 3 第二ドローローラ 4 引取ローラ 5 加熱蒸気処理器 6 温水浴 1 Feed Roller 2 First Draw Roller 3 Second Draw Roller 4 Take-up Roller 5 Heated Steam Processor 6 Hot Water Bath
Claims (2)
リエステル(A)とイソフタル酸1〜4.5 モル%とビス
フェノールAのエチレンオキシド付加物2〜7モル%と
を共重合したポリエステル(B)とが偏心的に接合して
おり、170 ℃における自由収縮熱処理での収縮率が15%
以下であり、かつ、170 ℃での弛緩熱処理により発現す
るスパイラル捲縮数が50個/25mm以上、伸度が25%以
下、強度が6.5 g/d以上である複合繊維を製造するに
際し、延伸を二段階で行い、トータル延伸倍率の70〜95
%の倍率で一段目の延伸を、続いて、加熱蒸気処理器内
を通過させながら、加熱蒸気温度130 〜170 ℃、滞留時
間0.5 秒以上として二段目の延伸を行うことを特徴とす
る潜在捲縮性ポリエステル複合繊維の製造方法。1. A polyester (A) mainly composed of ethylene terephthalate and an polyester (B) obtained by copolymerizing 1 to 4.5 mol% of isophthalic acid and 2 to 7 mol% of an ethylene oxide adduct of bisphenol A are eccentrically joined. And the shrinkage rate in free shrink heat treatment at 170 ° C is 15%.
In the production of a composite fiber having a number of spiral crimps of 50/25 mm or more, an elongation of 25% or less, and a strength of 6.5 g / d or more, which are not more than 170 ° C. The total draw ratio is 70-95.
%, The second stage is stretched at a heating steam temperature of 130 to 170 ° C and a residence time of 0.5 seconds or more while passing through the heating steam processor. Method for producing crimpable polyester conjugate fiber.
mmの機械捲縮を付与することを特徴とする請求項1記
載の潜在捲縮性ポリエステル複合繊維の製造方法。2. 8 to 18 pieces / 25 after the second stage drawing
The method for producing a latently crimpable polyester conjugate fiber according to claim 1, wherein a mechanical crimp of mm is applied.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6926896A JPH09228154A (en) | 1996-02-28 | 1996-02-28 | Production of polyester conjugate fiber with latent crimp tendency |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6926896A JPH09228154A (en) | 1996-02-28 | 1996-02-28 | Production of polyester conjugate fiber with latent crimp tendency |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH09228154A true JPH09228154A (en) | 1997-09-02 |
Family
ID=13397776
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6926896A Pending JPH09228154A (en) | 1996-02-28 | 1996-02-28 | Production of polyester conjugate fiber with latent crimp tendency |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH09228154A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003046266A1 (en) * | 2001-11-30 | 2003-06-05 | Teijin Limited | Machine crimped synthetic fiber having latent three-dimensional crimpability and method for production thereof |
-
1996
- 1996-02-28 JP JP6926896A patent/JPH09228154A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003046266A1 (en) * | 2001-11-30 | 2003-06-05 | Teijin Limited | Machine crimped synthetic fiber having latent three-dimensional crimpability and method for production thereof |
| CN100419144C (en) * | 2001-11-30 | 2008-09-17 | 帝人株式会社 | Machine-crimped synthetic fibers having latent three-dimensional crimping properties and method for producing same |
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