JP2005350777A - Polyester fiber - Google Patents
Polyester fiber Download PDFInfo
- Publication number
- JP2005350777A JP2005350777A JP2004151304A JP2004151304A JP2005350777A JP 2005350777 A JP2005350777 A JP 2005350777A JP 2004151304 A JP2004151304 A JP 2004151304A JP 2004151304 A JP2004151304 A JP 2004151304A JP 2005350777 A JP2005350777 A JP 2005350777A
- Authority
- JP
- Japan
- Prior art keywords
- polyester fiber
- fabric
- woven
- polyester
- shape
- 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 105
- 229920000728 polyester Polymers 0.000 title claims abstract description 75
- 239000002759 woven fabric Substances 0.000 claims abstract description 21
- 239000004744 fabric Substances 0.000 claims description 95
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 41
- 239000002245 particle Substances 0.000 claims description 29
- 238000009835 boiling Methods 0.000 claims description 11
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 7
- 239000011574 phosphorus Substances 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 claims description 5
- 238000000862 absorption spectrum Methods 0.000 claims description 4
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 238000009941 weaving Methods 0.000 abstract description 22
- 238000009940 knitting Methods 0.000 abstract description 5
- 238000000034 method Methods 0.000 description 37
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 15
- 238000002074 melt spinning Methods 0.000 description 10
- 239000000523 sample Substances 0.000 description 9
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 9
- 238000005809 transesterification reaction Methods 0.000 description 9
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 8
- -1 polyethylene terephthalate Polymers 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 description 7
- 239000005020 polyethylene terephthalate Substances 0.000 description 7
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 239000006224 matting agent Substances 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 238000009987 spinning Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 5
- 239000001639 calcium acetate Substances 0.000 description 5
- 229960005147 calcium acetate Drugs 0.000 description 5
- 235000011092 calcium acetate Nutrition 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- TXEDBPFZRNBYGP-UHFFFAOYSA-N dimethyl hydrogen phosphate;methyl dihydrogen phosphate Chemical compound COP(O)(O)=O.COP(O)(=O)OC TXEDBPFZRNBYGP-UHFFFAOYSA-N 0.000 description 5
- 230000001771 impaired effect Effects 0.000 description 5
- 238000000691 measurement method Methods 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 229910000410 antimony oxide Inorganic materials 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 229940043430 calcium compound Drugs 0.000 description 3
- 150000001674 calcium compounds Chemical class 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000013074 reference sample Substances 0.000 description 3
- 230000035807 sensation Effects 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000012790 confirmation Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 238000007707 calorimetry Methods 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000307 polymer substrate Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 238000005199 ultracentrifugation Methods 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 208000016261 weight loss Diseases 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Images
Landscapes
- Artificial Filaments (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
- Woven Fabrics (AREA)
Abstract
Description
本発明はポリエステル繊維に関し、更に詳しくは、清涼感、ハリコシ感、光沢感などを織編物に与えることができるポリエステル繊維に関する。 The present invention relates to a polyester fiber, and more particularly to a polyester fiber that can give a woven or knitted fabric a refreshing feeling, a firm feeling, and a glossy feeling.
従来、特にスポーツ衣料においては、織物に透湿性と防水性(耐水性)との両機能を同時に付与する方法として、樹脂コーティングやフィルムによるラミネートで撥水加工された織物表面に微多孔樹脂層を形成させる方法が多く行われている。しかし、この方法は、織物の表面に多数の層を形成するため、製造に多くの工程を必要とし、コスト高になることが避けられなかった。 Conventionally, particularly in sports clothing, as a method of simultaneously imparting both moisture permeability and waterproofing (water resistance) functions to a fabric, a microporous resin layer is applied to the surface of the fabric that has been water-repellent processed by resin coating or film lamination. Many methods of forming are performed. However, since this method forms a large number of layers on the surface of the woven fabric, many processes are required for production, and it is inevitable that the cost increases.
このような問題の対策として、繊維を織物にするだけで所望の機能が得られるようにしたものとして、単繊維繊度0.45dtex以下の丸断面極細マルチフィラメントを織物とすることにより、防風性と耐水圧を向上させる方法(例えば特許文献1参照)、また1.8dtexのW型異形断面フィラメントと0.25dtexの丸断面極細フィラメントの混繊マルチフィラメントを織物にすることにより耐水圧を向上させる方法(例えば特許文献2参照)などの提案がされている。 As a countermeasure against such a problem, the desired function can be obtained only by making the fiber into a woven fabric, and by making the round cross-sectional ultrafine multifilament having a single fiber fineness of 0.45 dtex or less into a woven fabric, A method for improving water pressure resistance (for example, see Patent Document 1), and a method for improving water pressure resistance by forming a mixed multifilament of 1.8 dtex W-shaped irregular cross-section filament and 0.25 dtex round cross-section ultrafine filament into a woven fabric. (For example, refer patent document 2) etc. are proposed.
しかしながら、これらの方法は、耐水圧の向上は可能になるものの、織物にヘタリを生じ、ハリコシ感がなくなるという欠点がある。また、単繊維断面を異形化したマルチフィラメントを用いて織物にすることにより、耐水性とソフト性などを得るという方法の提案もある(例えば特許文献3参照)。しかし、この方法も、耐水性は向上するものの、清涼感、光沢感、ハリコシ感が劣るという欠点を解決するものではなかった。 However, although these methods can improve the water pressure resistance, there is a drawback that the fabric is crushed and there is no harshness. There is also a proposal of a method of obtaining water resistance and softness by using a multifilament with a single fiber cross-section having a modified shape to obtain a woven fabric (see, for example, Patent Document 3). However, this method also improves the water resistance, but does not solve the drawbacks of inferior refreshing feeling, glossiness, and harshness.
また、従来の室内インテリア用カーテンにおいては、障子で得られるような遮像性と採光性を併せ持つ効果は達成できていない。そのため、昼間の適度な明るさと外からの見え難さを兼備させることを目的にした目開きを有する室内インテリア用薄地カーテンとしては、様々な柄を糸あるいは織編構造で演出するレースカーテンが主流になっている。 Moreover, in the conventional curtain for indoor interiors, the effect which has both image-shielding property and daylighting property which can be obtained with a shoji cannot be achieved. For this reason, lace curtains that produce various patterns with yarn or woven knitting structure are the mainstream for indoor interior thin curtains that have an opening that aims to combine moderate brightness in the daytime and difficult to see from the outside. It has become.
目開きの織編物としては、ボイル織物と呼ばれる織物がある。しかし、この織物は使用する経糸および緯糸がともに撚数が800回/m以上であるため、糸同士の摩擦抵抗が高く、織物の経糸と緯糸との交点における拘束力が高くなること、ボイルによる加熱により、織物の形態安定性が向上することから、風合いが硬くなってしまうという問題がある。そのため、カーテンを吊した際にウェーブの曲がりの直径が大きくなり、深くきれいなウェーブおよび風に軽くなびくような演出がし難くなる欠点がある。これを解消するためアルカリ減量処理を施して、織物を構成する繊維を細くすることでカーテン織物の風合いを柔らかくする技術もあるが、満足すべき柔らかさは得にくく、かつ工程が増えるため製造コストが高くなってしまう。 As a woven or knitted fabric with openings, there is a fabric called a boiled fabric. However, since both the warp and the weft used in this woven fabric have a twist number of 800 times / m or more, the frictional resistance between the yarns is high, and the binding force at the intersection of the woven warp and the weft is high. Since the morphological stability of the fabric is improved by heating, there is a problem that the texture becomes hard. For this reason, when the curtain is hung, there is a drawback that the diameter of the wave bend becomes large, and it is difficult to produce a deep and beautiful wave and a light fluttering in the wind. In order to solve this problem, there is a technology to soften the texture of the curtain fabric by applying alkali weight reduction treatment and making the fibers that make up the fabric thinner. However, it is difficult to obtain satisfactory softness and the number of processes increases, so the manufacturing cost is increased. Becomes higher.
上記のような背景から、熱水収縮率5%以下のポリエステル繊維を用い、製織条件を適正化することにより、風合いの柔らかいカーテン用織物を提供するようにした方法が提案されている(例えば、特許文献4参照)。しかし、この方法では、一定間隔の深くきれいなウェーブを形成するカーテン用織物とはなるものの、遮像性、採光性を実現することはできなかった。
本発明の目的は、上述した従来技術の問題を解決し、高密度に製織するだけで優れた耐水性を付与した上に、清涼感、ハリコシ感、光沢感の付与を可能にするポリエステル繊維及びポリエステル繊維織物を提供することにある。 The object of the present invention is to solve the above-mentioned problems of the prior art, and to impart excellent water resistance only by weaving at a high density, and also to provide a refreshing feeling, a harsh feeling, and a glossy feeling, It is to provide a polyester fiber fabric.
また、本発明の他の目的は、低密度に織編するだけで風合いが柔らかく、良好なウェーブを形成し、かつ遮像性と採光性とを同時に備えた上に、清涼感、ハリコシ感、光沢感の付与を可能にするポリエステル繊維、特にカーテン用織編物用として好適なポリエステル繊維を提供することにある。 Another object of the present invention is that the texture is soft just by weaving and knitting at a low density, forming a good wave, and having both the image-shielding property and the daylighting property. It is an object of the present invention to provide a polyester fiber that can give a glossy feeling, particularly a polyester fiber suitable for woven or knitted fabric for curtains.
上記目的を達成する本発明のポリエステル繊維は、単繊維繊度が2.5dtex以下で、単繊維断面形状が六〜十葉の扁平多葉形であり、該扁平多葉形の外接円の頂点間を結ぶ最長の長径をA、該長径Aに直交すると共に前記扁平多葉形の凸部の頂点間を結ぶ短径のうち最大の短径をB、該短径Bと同一か又は2番目に長い短径をC、かつ前記扁平多葉形の凹部の底点間を結ぶ短径のうちの最短の短径をDとするとき、下記式を満足するようにした単繊維からなり、かつ該単繊維の光沢度が35〜70であることを特徴とするものである。
扁平度(A/B)=1.2〜2.2
異形度I(C/D)=1.1〜1.3
異形度II(B/D)=1.1〜1.6
A>B≧C>D
The polyester fiber of the present invention that achieves the above object is a flat multilobal shape having a single fiber fineness of 2.5 dtex or less and a single fiber cross-sectional shape of 6 to 10 leaves, and between the vertices of the circumscribed circle of the flat multileaf shape A is the longest major axis connecting A, and B is the largest minor axis among the minor diameters orthogonal to the major axis A and connecting the vertices of the flat multilobed convex portions. When the shortest short diameter out of the short diameters connecting the bottoms of the flat multilobed recesses is D, the long short diameter is made of a single fiber that satisfies the following formula; The single fiber has a glossiness of 35 to 70.
Flatness (A / B) = 1.2 to 2.2
Deformation degree I (C / D) = 1.1 to 1.3
Deformation degree II (B / D) = 1.1 to 1.6
A> B ≧ C> D
本発明のポリエステル繊維によれば、上記のように単繊維繊度が小さく、扁平度(A/B)と異形度I,IIが特定された扁平多葉断面を有し、かつ光沢度が35〜70である単繊維によりポリエステル繊維を構成したことにより、このポリエステル繊維を高密度に製織するだけで優れた耐水性を具備した上に、優れた清涼感、ハリコシ感、光沢感を有する織物にすることができる。 According to the polyester fiber of the present invention, the single fiber fineness is small as described above, the flatness (A / B) and the irregularities I and II are specified, and the glossiness is 35 to 35. By forming the polyester fiber with a single fiber of 70, the polyester fiber has excellent water resistance just by weaving the polyester fiber at a high density, and it is made into a woven fabric having excellent refreshing feeling, harshness feeling, and glossiness. be able to.
また、本発明のポリエステル繊維によれば、上記構成を有することにより、このポリエステル繊維を低密度に織編するだけで風合いが柔らかく、良好なウェーブを形成し、かつ遮像性と採光性とを同時に備えるようにした上に、優れた清涼感、ハリコシ感、光沢感を有する織編物にすることができ、特にカーテン用に適した優れた織編物にすることができる。 In addition, according to the polyester fiber of the present invention, by having the above-described configuration, the texture is soft just by weaving and knitting the polyester fiber at a low density, and a good wave is formed. In addition to being provided at the same time, it is possible to obtain a woven or knitted fabric having excellent refreshing sensation, harshness and glossiness, and particularly to an excellent woven or knitted fabric suitable for curtains.
本発明のポリエステル繊維に使用するポリエステルは、繊維形成性のポリエステルであれば特に限定されるものではない。例えば、ポリエチレンテレフタレート、ポリブチレンテレフタレート等を使用することができ、また繊維の特性を損なわない範囲で共重合成分を含有するものであってもよい。 The polyester used for the polyester fiber of the present invention is not particularly limited as long as it is a fiber-forming polyester. For example, polyethylene terephthalate, polybutylene terephthalate, or the like can be used, and a copolymer component may be contained as long as the properties of the fiber are not impaired.
本発明のポリエステル繊維は、繊維軸方向に対して直交する断面での単繊維断面形状が、図1に例示するような六〜十葉の扁平多葉形であり、好ましくは六〜八葉の扁平多葉断面形を有する。このような扁平多葉断面形を有することにより、フィラメント外周に凸部と凹部を交互に形成し、良好な光沢を発揮することができる。特に、六〜八葉の扁平断面のものは、いぶし銀様の光沢を発現することができる。とりわけ、扁平八葉断面の場合は、高級感のある光沢を発現することができる。 In the polyester fiber of the present invention, the single fiber cross-sectional shape in a cross section orthogonal to the fiber axis direction is a flat multilobal shape of 6 to 10 leaves as exemplified in FIG. 1, and preferably 6 to 8 leaves. It has a flat multilobal cross-sectional shape. By having such a flat multilobal cross-sectional shape, convex portions and concave portions are alternately formed on the outer periphery of the filament, and good gloss can be exhibited. In particular, those having a flat cross section of 6 to 8 leaves can express a silver-like luster. In particular, in the case of a flat eight-leaf cross section, a gloss with a high-class feeling can be expressed.
また、本発明のポリエステル繊維は、構成材料であるポリエステルに艶消し剤を配合しないことにより、凹凸部による光沢作用と相乗して一層高い光沢感を呈することができ、後述する光沢度として35〜70、より好ましくは45〜65の高いレベルにすることができる。光沢度が35未満ではマイルドな光沢感が得られなくなり、また70を超えると、高密度織物にした場合、糸のイラツキが強くなりマイルドさが低減する。 Further, the polyester fiber of the present invention can exhibit a higher gloss feeling in synergy with the glossy action by the concavo-convex part by not adding a matting agent to the polyester which is a constituent material. It can be as high as 70, more preferably 45-65. When the glossiness is less than 35, a mild glossy feeling cannot be obtained. When the glossiness is more than 70, the yarn becomes more irritated and the mildness is reduced when a high-density fabric is used.
本発明のポリエステル繊維は、更に六〜十葉の扁平多葉断面に形成されていることにより適度の剛性を発揮し、織物又は編物にしたときにはヘタリ難く、優れたハリコシ感を有する。更に、フィラメント表面に形成された多数の凹部は、織物又は編物にしたときサラッとした風合いにし、織編物の表面に肌が軽く触れた際に「サラサラ」とした感触を与える。更に強く触れた際には、適度の「きしみ」を感じさせる。これらの「サラサラ」感や「きしみ」感の風合いを「清涼感」と称する。 The polyester fiber of the present invention further exhibits appropriate rigidity by being formed in a flat multilobal cross section of 6 to 10 leaves, and when it is made into a woven fabric or a knitted fabric, it is difficult to stick and has an excellent feeling of elasticity. Furthermore, a large number of recesses formed on the filament surface give a smooth texture when made into a woven or knitted fabric, and give a “smooth” feel when the surface of the woven or knitted fabric is lightly touched. When touched more strongly, it feels moderate “squeak”. The texture of these “smooth” feeling and “squeaky” feeling is referred to as “cool feeling”.
本発明のポリエステル繊維は、上述した光沢度35〜70の光沢感、ハリコシ感、清涼感を満たすため、単繊維断面における扁平多葉断面形状を外接円で囲んだときの長径と短径とが以下に説明するような関係になっていなければならない。 The polyester fiber of the present invention has a long diameter and a short diameter when the flat multi-leaf cross-sectional shape in a single fiber cross-section is surrounded by a circumscribed circle in order to satisfy the above-described glossiness of 35 to 70, crispness, and refreshing feeling. The relationship must be as described below.
図1(A)、(B)、(C)に、単繊維断面の代表例を示すが、この単繊維断面形状が六〜十葉の扁平多葉形であって、下記式を満足する単繊維からなる。
扁平度(A/B)=1.2〜2.2
異形度I(C/D)=1.1〜1.3
異形度II(B/D)=1.1〜1.6
A>B≧C>D
1 (A), (B), and (C) show typical examples of a single fiber cross section. This single fiber cross section is a flat multilobal shape of six to ten lobes, and a single fiber satisfying the following formula: Made of fiber.
Flatness (A / B) = 1.2 to 2.2
Deformation degree I (C / D) = 1.1 to 1.3
Deformation degree II (B / D) = 1.1 to 1.6
A> B ≧ C> D
ここで、Aは上記扁平多葉形の外接円の頂点間を結ぶ最長の長径である。また、Bは長径Aの方向に直交すると共に扁平多葉形の凸部の頂点間を結ぶ短径のうち最大の短径をいう。Cは短径Bと同一長さであるか又は2番目に長い短径をいう。また、Dは扁平多葉形の凹部の底点間を結ぶ短径のうち最短の短径をいう。 Here, A is the longest major axis connecting the vertices of the circumscribed circle of the flat multilobal shape. Further, B is the largest minor axis among the minor axes that are orthogonal to the direction of the major axis A and connect the apexes of the flat multilobed convex portions. C is the same length as the minor axis B or the second minor axis. Further, D is the shortest short diameter among the short diameters connecting the bottom points of the flat multilobed concave portions.
扁平度(A/B)が1.2未満であると、光沢感の向上効果が認められなくなり、また2.2を超えると、織物又は編物にしたときのハリコシ感が小さく、ヘタリやすくなる。また、製糸性の悪化や糸条の解舒性が悪化する。扁平度(A/B)は、より好ましくは1.3〜2.1であり、更に好ましくは1.4〜2.0にするのがよい。また、異形度I(C/D)が1.3より大きくなったり、異形度II(B/D)が1.6より大きくなると光沢感が低下する。また、高次工程での擦過、また衣服の着用や洗濯などで凸部が摩滅し繊維断面が変化したり、フィブリル化が起こりやすくなる。 When the flatness (A / B) is less than 1.2, the effect of improving the glossiness is not recognized. When the flatness (A / B) exceeds 2.2, the harshness of the woven fabric or knitted fabric is small, and it becomes easy to wear. In addition, the yarn-making property is deteriorated and the unwinding property of the yarn is deteriorated. The flatness (A / B) is more preferably 1.3 to 2.1, and still more preferably 1.4 to 2.0. Further, when the irregularity degree I (C / D) is larger than 1.3 or the irregularity degree II (B / D) is larger than 1.6, the glossiness is lowered. In addition, the convex portions are worn away by rubbing in higher-order processes, wearing or washing clothes, and the fiber cross section is changed, and fibrillation tends to occur.
本発明のポリエステル繊維には、後述する測定法で測定されたときのカルシウム元素を2〜20重量%とリン元素を2〜20重量%からなる特定の内部粒子を繊維中に0.03〜0.5重量%含有することが好ましい。更に好ましくは、0.05〜0.3重量%である。この内部粒子の含有量が0.03重量%未満では、紡糸を行って複屈折13×10-3〜80×10-3の配向糸を生産するとき、溶融紡糸時の流動安定性が十分でなく、またガラス転移点以上融点以下での熱変形性も十分でなく好ましくない。 In the polyester fiber of the present invention, specific internal particles composed of 2 to 20% by weight of calcium element and 2 to 20% by weight of phosphorus element when measured by the measurement method described later are 0.03 to 0 in the fiber. It is preferable to contain 5% by weight. More preferably, it is 0.05 to 0.3% by weight. When the content of the internal particles is less than 0.03% by weight, the flow stability during melt spinning is sufficient when spinning is performed to produce oriented yarns having birefringence of 13 × 10 −3 to 80 × 10 −3. In addition, the thermal deformation at the glass transition point or higher and below the melting point is not sufficient and not preferable.
上記内部粒子中のリン元素量が2重量%未満の場合は、生成する粒子が粗大化しやすくなる。このため溶融紡糸時の流動安定性、ガラス転移点以上融点以下での熱変形性が欠如しやすくなる。この理由はカルシウム系内部粒子中にリンが存在してくることにより粒子のポリマ基質に対する親和性が一層強まり、そのため粒子の凝集、粗大化が起こりにくくなるためと考えられるが、もちろん本発明は上記理由に限定されるものではない。 When the amount of phosphorus element in the internal particles is less than 2% by weight, the generated particles are easily coarsened. For this reason, it becomes easy to lack the flow stability at the time of melt spinning, and the heat deformability at the glass transition point or higher and below the melting point. The reason for this is considered to be that the presence of phosphorus in the calcium-based inner particles further increases the affinity of the particles for the polymer substrate, and therefore, aggregation and coarsening of the particles are less likely to occur. It is not limited to the reason.
一方、内部粒子中のカルシウム元素が2重量%未満であったり、或いはリン元素量が20重量%を越える場合は、生成した粒子の性質が基体ポリエステルに近似し過ぎ、ポリエステル成分に溶解していくための必要十分な粒子量が確保できず、そのため溶融紡糸時の流動安定性、ガラス転移点以上融点以下の熱変形性に欠如しやすくなる。 On the other hand, when the amount of calcium element in the internal particles is less than 2% by weight or the amount of phosphorus element exceeds 20% by weight, the properties of the generated particles are too close to the base polyester and dissolve in the polyester component. Therefore, the necessary and sufficient amount of particles cannot be ensured, so that the flow stability at the time of melt spinning and the heat deformability from the glass transition point to the melting point or less tend to be lacking.
また、上記内部粒子は、分離した内部粒子について測定した赤外吸収スペクトルのカルボニル基の二重結合の伸縮振動が金属元素に隣接した際に起こる1600cm-1の吸収を実質的に持たないことが好ましい。 Further, the internal particles may have substantially no absorption at 1600 cm −1 that occurs when the stretching vibration of the double bond of the carbonyl group in the infrared absorption spectrum measured for the separated internal particles is adjacent to the metal element. preferable.
〔内部粒子量の測定方法〕
溶融紡糸によって得られた複屈折13×10-3〜80×10-3の配向糸をメタノールで十分洗浄し、油剤を取り除き、水洗し、乾燥する。このポリエステル繊維300gを採取し、これにo−クロロフェノール2.7kgを加えて撹拌しつつ100℃まで昇温し、昇温後更に1時間そのまま放置してポリマ部分を溶解させる。
[Method for measuring the amount of internal particles]
An oriented yarn having a birefringence of 13 × 10 −3 to 80 × 10 −3 obtained by melt spinning is sufficiently washed with methanol, the oil agent is removed, washed with water, and dried. 300 g of this polyester fiber is sampled, 2.7 kg of o-chlorophenol is added thereto, and the temperature is raised to 100 ° C. while stirring. After the temperature rise, the polymer portion is allowed to stand for 1 hour.
ただし、この条件では高度に結晶化している場合など十分ポリマ部分を溶融してから急冷したものを試料として上記溶解条件で行うことができる。次いで、ポリマ中に含有されているゴミ、あるいは添加されている補強剤等内部粒子以外の不溶物除去のため溶液をG−3ガラスフィルターで濾過し、この重量は試料量から差し引く。 However, under these conditions, the polymer portion can be melted and then rapidly cooled after being sufficiently crystallized, and the sample can be obtained under the above-mentioned dissolution conditions. Next, the solution is filtered with a G-3 glass filter to remove insoluble matters other than internal particles such as dust contained in the polymer or added reinforcing agent, and this weight is subtracted from the sample amount.
日立製作所製分離用超遠心機40P型にローターRP30を装備し、セル1個当たりに上記溶液3.0ccを注入後、ローターを4500rpmに回転させ、回転異常のないことを確認後、ローター中を真空にし、30000rpmに回転数を上げ、この回転数にて粒子の遠心分離を行う。分離の完了はほぼ40分後であるがこの確認は必要あれば分離後の液の375mμにおけ光線透過率が分離前のそれに対し、高い値の一定値になることで行う。 The rotor RP30 is installed in the separation ultracentrifuge 40P type manufactured by Hitachi, Ltd. After injecting 3.0 cc of the above solution per cell, the rotor is rotated to 4500 rpm, and after confirming that there is no abnormal rotation, Vacuum is applied, the rotational speed is increased to 30000 rpm, and the particles are centrifuged at this rotational speed. Separation is completed after about 40 minutes, but this confirmation is made if necessary, by confirming that the light transmittance at 375 mμ of the liquid after separation becomes a constant value higher than that before separation.
分離後、上澄液を傾斜法で除去し分離粒子を得る。 After separation, the supernatant is removed by a gradient method to obtain separated particles.
分離粒子には分離不十分の理由によるポリマ分の混入があり得るので、採取した該粒子に常温のo−クロロフェノールを加え、ほぼ均一懸濁後、再び超遠心分離機処理を行う。 Since the separated particles may be mixed with a polymer due to insufficient separation, normal temperature o-chlorophenol is added to the collected particles, and the suspension is subjected to ultracentrifugation again after almost uniform suspension.
この操作は粒子を該粒子を乾燥後に粒子分を走査型差動熱量分析にてポリマに相当する融解ピークが検出できなくなるまで繰り返す必要がある。 This operation needs to be repeated after the particles have been dried until the melting point corresponding to the polymer can no longer be detected by scanning differential calorimetry.
最後に、このようにして得た分離粒子を120℃、16時間真空乾燥して秤量する。 Finally, the separated particles thus obtained are vacuum-dried at 120 ° C. for 16 hours and weighed.
〔赤外吸収スペクトルの測定法〕
試料0.8mgをKBr300mgとともに常法によりプレスし、KBr錠剤を作成して日立赤外分光光度計EP1−2型で岩塩プリズムを用い、波長領域650〜4000cm-1で測定する。
[Measurement method of infrared absorption spectrum]
0.8 mg of a sample is pressed together with 300 mg of KBr by a conventional method, a KBr tablet is prepared, and measured in a wavelength region of 650 to 4000 cm −1 using a rock salt prism with a Hitachi infrared spectrophotometer EP1-2 type.
本発明のポリエステル繊維を製造するにあたっては、次のような条件をとることが好ましい。 In producing the polyester fiber of the present invention, it is preferable to take the following conditions.
すなわち、テレフタル酸の低級アルキルエステルとエチレングリコールからポリエステルを製造するに際し、エステル交換終了後、カルシウム化合物の存在下、亜リン酸およびリン酸メチルエステルを次の(1)、(2)、(3)式を満足する量を添加して重合触媒の存在下にて重合させる方法である。
(1) 6×10-6≦3X+2Y≦30×10-6
(2) 0.25×10-6≦X≦5×10-6
(3) 0.5×10-6≦Y≦10×10-6
(ただし、Xはテレフタル酸の低級アルキルエステル1gに対する亜リン酸のモル数を表し、Yはリン酸メチルエステルのモル数を表す。)
That is, when a polyester is produced from a lower alkyl ester of terephthalic acid and ethylene glycol, phosphoric acid and phosphoric acid methyl ester are converted into the following (1), (2), (3) in the presence of a calcium compound after transesterification. ) In the presence of a polymerization catalyst by adding an amount satisfying the formula.
(1) 6 × 10 −6 ≦ 3X + 2Y ≦ 30 × 10 −6
(2) 0.25 × 10 −6 ≦ X ≦ 5 × 10 −6
(3) 0.5 × 10 −6 ≦ Y ≦ 10 × 10 −6
(However, X represents the number of moles of phosphorous acid relative to 1 g of the lower alkyl ester of terephthalic acid, and Y represents the number of moles of phosphoric acid methyl ester.)
なお、カルシウム化合物はエステル交換触媒として用いても、また他の金属化合物をエステル交換触媒として用い、エステル交換終了後添加してもよい。カルシウム化合物は反応系に可溶なものであればよい。特に酢酸カルシウム、塩化カルシウム、水素化カルシウムが好ましい。 The calcium compound may be used as a transesterification catalyst, or another metal compound may be used as a transesterification catalyst and added after completion of transesterification. Any calcium compound may be used as long as it is soluble in the reaction system. In particular, calcium acetate, calcium chloride, and calcium hydride are preferable.
亜リン酸およびリン酸のメチルエステルの添加はエステル交換反応後に行われるが、重縮合反応があまり進まないうちに終了することが好ましい。亜リン酸とリン酸のメチルエステルに同時に添加しても別個に添加してもよく、また分割して添加することもできる。なお、リン酸のメチルエステルとしてはトリメチルホスヘートが好ましく使用される。 The addition of phosphorous acid and methyl ester of phosphoric acid is carried out after the transesterification reaction, but it is preferably completed before the polycondensation reaction proceeds so much. The phosphorous acid and phosphoric acid methyl ester may be added simultaneously or separately, or may be added separately. Trimethyl phosphate is preferably used as the methyl ester of phosphoric acid.
亜リン酸の添加量が0.25×10-6未満では、内部粒子中のカルシウム元素量が20%を越え、かつリン元素量が2%未満となり、また5×10-6を越えるとポリマが黒ずみやすくなる。また、リン酸メチルエステルの添加量が0.5×10-6未満の場合は、内部粒子量が0.5%を越える量以上となり、また10×10-6を越えるとカルシウム元素量が2%未満でかつリン元素量が20%を越える量以上になり、光沢感が損なわれる傾向になる。 If the amount of phosphorous acid added is less than 0.25 × 10 −6 , the amount of calcium element in the internal particles exceeds 20% and the amount of phosphorus element is less than 2%, and if it exceeds 5 × 10 −6 , Becomes darker. When the amount of phosphoric acid methyl ester added is less than 0.5 × 10 −6 , the amount of internal particles exceeds 0.5%, and when it exceeds 10 × 10 −6 , the amount of calcium element is 2 % And the amount of phosphorus element exceeds 20%, the glossiness tends to be impaired.
そして、亜リン酸とリン酸メチルエステル両者の添加量比が(1)式の下限から外れると内部粒子の赤外吸収スペクトルに1600cm-1の吸収が現れ、(1)式の上限から外れると内部粒子量が0.03%以下でポリマの重合生産性が低下しやすくなる。 And when the addition ratio of both phosphorous acid and phosphoric acid methyl ester deviates from the lower limit of the formula (1), absorption of 1600 cm −1 appears in the infrared absorption spectrum of the internal particles, and deviates from the upper limit of the formula (1). When the amount of internal particles is 0.03% or less, the polymerization productivity of the polymer tends to decrease.
すなわち、内部粒子は添加した物質がそのまま粒子となるのではなく、ポリエステル合成反応系中での反応変性によって析出するため、添加物質の組成如何によって粒子の量及び、粒子の生成が大きく変化しやすくなり、その結果、本発明のポリエステル繊維の特徴である光沢感、耐水性が損なわれる傾向になる。 In other words, the added particles do not become particles as they are, but precipitate due to reaction modification in the polyester synthesis reaction system, so the amount of particles and the generation of particles are likely to change greatly depending on the composition of the added materials. As a result, the glossiness and water resistance which are the characteristics of the polyester fiber of the present invention tend to be impaired.
このような本発明のポリエステル繊維の工程通過性や、それから得られる製品品位の向上効果については、複屈折が13×10-3未満の場合、延伸および延伸仮撚り加工にて毛羽が発生しやすくなる。一方、複屈折が80×10-3を越える場合、高配向となり、延伸や延伸仮撚り加工で毛羽、糸切れが発生し、均一性が損なわれやすくなる。 Regarding the process passability of the polyester fiber of the present invention and the effect of improving the product quality obtained therefrom, when the birefringence is less than 13 × 10 −3, fluff is likely to occur during stretching and stretching false twisting. Become. On the other hand, when the birefringence exceeds 80 × 10 −3 , high orientation is obtained, and fluff and yarn breakage are generated by stretching or stretching false twisting, and uniformity is easily impaired.
本発明のポリエステル繊維は、単繊維繊度が2.5dtex以下の細繊度であることが必要である。単繊維繊度が2.5dtexより大きいと、粗硬感が生じて肌と接触すると不快感となり、清涼感が得られなくなる。また、織物にしたとき単糸間に空隙を生じ易くなるため、耐水性が低下することになる。しかし、単繊維繊度があまり小さくなっても、耐摩擦性などが低下するため、単繊維繊度の下限としては、0.5dtexであることが好ましい。 The polyester fiber of the present invention needs to have a fineness of single fiber fineness of 2.5 dtex or less. When the single fiber fineness is larger than 2.5 dtex, a feeling of coarseness is generated, and when it comes into contact with the skin, it becomes uncomfortable and a refreshing feeling cannot be obtained. Moreover, since it becomes easy to produce a space | gap between single yarn when it is set as a textile fabric, water resistance will fall. However, even if the single fiber fineness is too small, the friction resistance and the like are lowered. Therefore, the lower limit of the single fiber fineness is preferably 0.5 dtex.
ポリエステル繊維の総繊度は特に限定されるものではないが、好ましくは56〜167dtexの範囲がよい。特に、総繊度を84dtex程度にしたものでは、特に高密度織物にした場合の耐水性を最も良好にすることができる。また、110tex程度にしたものでは、特にカーテン用として低密度の織編物にしたときの遮光性及び採光性を最も良好にすることができる。 The total fineness of the polyester fiber is not particularly limited, but is preferably in the range of 56 to 167 dtex. In particular, when the total fineness is set to about 84 dtex, the water resistance can be made most favorable when a high-density fabric is used. In addition, in the case of about 110 tex, the light shielding property and the daylighting property can be made most favorable when a low-density woven or knitted fabric is used particularly for curtains.
ポリエステル繊維の強度及び伸度は特に限定されるものではないが、好ましくは、強度は3〜7cN/dtexにするのがよい。特に、高密度織物の場合には、堅ろう性の面から4.5cN/dtex程度が好ましい。また、伸度は18〜40%の範囲が好ましい。特に、高密度織物やカーテン用織編物の風合いを良好にする上では22〜30%程度にするのがよい。 The strength and elongation of the polyester fiber are not particularly limited, but preferably the strength is 3 to 7 cN / dtex. In particular, in the case of a high-density woven fabric, about 4.5 cN / dtex is preferable from the viewpoint of fastness. Further, the elongation is preferably in the range of 18 to 40%. In particular, in order to improve the texture of the high-density woven fabric and the woven or knitted fabric for curtains, the content is preferably about 22 to 30%.
また、本発明のポリエステル繊維は、沸騰水収縮率が5%以下であることが好ましい。沸騰水収縮率が5%より大きいと、織物を精錬及び染色する際、又は編物を染色する際に繊維の収縮により織物が硬くなり、風合いが損なわれやすくなる。また、繊維の収縮により織編物の型崩れが生じ、均一な織編密度が得られなくなるため、高密度織物の場合には耐水性が低下し、またカーテン用織編物の場合には遮光性及び採光性が低下する傾向になる。 Further, the polyester fiber of the present invention preferably has a boiling water shrinkage of 5% or less. When the boiling water shrinkage ratio is larger than 5%, the fabric becomes hard due to the shrinkage of the fiber when the fabric is refined and dyed, or when the knitted fabric is dyed, and the texture tends to be impaired. In addition, since the woven or knitted fabric loses its shape due to the shrinkage of the fiber, and a uniform woven or knitted density cannot be obtained, the water resistance decreases in the case of a high-density woven fabric, and in the case of a woven or knitted fabric for curtains, There is a tendency for daylighting to decrease.
上述したポリエステル繊維の製造方法は特に限定されるものではないが、好ましくは溶融紡糸法によって製糸することができる。溶融紡糸口金の吐出孔としては、図2(A)や(B)に示すような形状のものが好ましく使用される。例えば、図2(A)の吐出孔の場合には、図1(A)のような単繊維断面のフィラメントが得られ、また図2(B)の吐出孔の場合には、図1(C)のような単繊維断面のフィラメントが得られる。 Although the manufacturing method of the polyester fiber mentioned above is not specifically limited, Preferably it can manufacture by a melt spinning method. As the discharge hole of the melt spinneret, those having a shape as shown in FIGS. 2A and 2B are preferably used. For example, in the case of the discharge hole in FIG. 2A, a filament having a single fiber cross section as shown in FIG. 1A is obtained, and in the case of the discharge hole in FIG. A filament having a single fiber cross section as shown in FIG.
溶融紡糸工程は、図3あるいは図4のようにして製糸することができる。図3の溶融紡糸工程では、溶融状態のポリエステルを紡糸パック1の紡糸口金2から、それぞれ二つの糸条として吐出し、その二つの糸条を冷却チムニー3で冷却空気により冷却固化した後、それぞれ給油ガイド4、4で紡糸油剤を付与し、インターレースノズル5、5によりそれぞれの糸条に交絡を付与しながら引取ローラー6で引き取り、最後に糸条毎にパッケージ7、7に巻き上げる。引取ローラー6における引取速度としては、2500〜3500m/minが適用される。パッケージ7に巻き取られた糸条は、次いで延伸工程において数倍に延伸されることにより、本発明のポリエステル繊維が得られる。
In the melt spinning step, yarn can be produced as shown in FIG. 3 or FIG. In the melt spinning step of FIG. 3, the melted polyester is discharged from the
図4の溶融紡糸工程では、紡糸口金2から吐出された二つの糸条を一本の糸条として収束し、1個のパッケージ7に巻き取るようにした点が図3の工程とは相違している。
The melt spinning process of FIG. 4 is different from the process of FIG. 3 in that the two yarns discharged from the
本発明のポリエステル繊維を経糸及び/又は緯糸に使用して、高密度織物に製織する場合には、製織するだけで高い耐水性を付与すると共に、清涼感、ハリコシ感、光沢感に優れた織物を得ることができる。 When the polyester fiber of the present invention is used for warp and / or weft to be woven into a high-density fabric, the fabric provides high water resistance just by weaving and is excellent in coolness, harshness and gloss. Can be obtained.
高密度織物における経糸のカバーファクターWCFは1450〜1700の範囲、緯糸のカバーファクターFCFは870〜1150の範囲にする。また、両カバーファクターの比FCF/WCFを0.60〜0.68の範囲にするものとする。ここで、経糸のカバーファクター(WCF)及び経糸のカバーファクター(FCF)は、次のように定義されるものである。
WCF=WN×√(WD)
FCF=FN×√(FD)
The cover factor WCF of the warp in the high-density fabric is in the range of 1450-1700, and the cover factor FCF of the weft is in the range of 870-1150. Further, the ratio FCF / WCF of both cover factors shall be in the range of 0.60 to 0.68. Here, the warp cover factor (WCF) and the warp cover factor (FCF) are defined as follows.
WCF = WN × √ (WD)
FCF = FN × √ (FD)
ただし、上記式において、WNは経糸の製品織密度(25mm当たりの経糸本数)、WDは経糸の製織前のトータル繊度、FNは緯糸の製品織密度(25mm当たりの緯糸本数)、FDは緯糸の製織前のトータル繊度を示す。 However, in the above formula, WN is the product weave density of the warp (number of warps per 25 mm), WD is the total fineness before weaving the warp, FN is the product weave density of the weft (number of wefts per 25 mm), and FD is the weft of the weft Indicates the total fineness before weaving.
本発明のポリエステル繊維を高密度織物にするときの製織方法は、特に限定されない。エアジェットルーム(AJL)、ウオータージェットルーム(WJL)等の公知の織機をいずれも用いて製造することができる。 The weaving method when making the polyester fiber of the present invention a high-density fabric is not particularly limited. Any known loom such as an air jet loom (AJL) or a water jet loom (WJL) can be used.
本発明のポリエステル繊維を用いて製織された高密度織物は、JIS−L−1092Aに基づく耐水圧を5.0kPa以上にした上に、優れた清涼感、ハリコシ感、光沢感を有するものにすることができる。より好ましくは、耐水圧を6.0kPa以上にすることができ、スポーツ衣料用の布帛として有効に展開することができる。 The high-density fabric woven using the polyester fiber of the present invention has excellent water-cooling pressure based on JIS-L-1092A of 5.0 kPa or more, and also has excellent refreshing feeling, harshness, and glossiness. be able to. More preferably, the water pressure resistance can be set to 6.0 kPa or more, and it can be effectively developed as a fabric for sports clothing.
他方、本発明のポリエステル繊維をカーテン用織編物にする場合には、このポリエステル繊維を低密度で、遮像効果を示すLb値が10〜25%に、また採光率が30%〜45%なるように製織または編成するだけで所望とする遮像性と採光性とを併せ持つ織編物にすることができる。織編物の密度としては、織物の場合には経緯の織密度で60〜100本/25mm、編物の場合には30〜60コース/25mmが好ましい。 On the other hand, when the polyester fiber of the present invention is used as a woven or knitted fabric for curtains, the polyester fiber has a low density, the Lb value indicating the image shielding effect is 10 to 25%, and the lighting rate is 30% to 45%. Thus, a woven or knitted fabric having both desired image-shielding properties and daylighting properties can be obtained simply by weaving or knitting. The density of the woven or knitted fabric is preferably 60 to 100 yarns / 25 mm in the case of a woven fabric, and 30 to 60 courses / 25 mm in the case of a knitted fabric.
Lb値が10%未満であると遮像効果は顕著に向上するが、採光性が低下しやすく、所望とする遮像性と採光性とを併せ持つ織編物にすることが難しくなる。また、Lb値が25%を超えると遮像効果が低下しやすくなる。また、採光率が30%未満であると、カーテンとした際に室内の明るさが不足しやすくなる。また、採光率が45%を超えると、室内の明るさは充分であるが、遮像効果が低下しやすくなる。なお、Lb値と採光率は後述する測定法により測定されたものである。 When the Lb value is less than 10%, the image-shielding effect is remarkably improved, but the daylighting property tends to be lowered, and it becomes difficult to obtain a woven or knitted fabric having both desired image-shielding property and daylighting property. On the other hand, if the Lb value exceeds 25%, the image shielding effect tends to be lowered. Moreover, when the lighting ratio is less than 30%, the room brightness tends to be insufficient when the curtain is used. On the other hand, if the lighting ratio exceeds 45%, the indoor brightness is sufficient, but the image-shielding effect tends to be reduced. The Lb value and the daylighting rate are measured by the measurement method described later.
本発明のポリエステル繊維を用いたカーテン用織編物の織物組織や編地組織は特に限定されるものではなく、織物組織としては、平織、斜文織(綾織、ツイル)、朱子織(サテン)などのいずれも用いることができる。また、編地組織としては、経編地であるトリコット地やラッセル地、丸編地であるシングル丸編地、ダブル丸編地などのいずれも用いることができるが、生地が薄くて寸法安定性に優れた経編地が好ましく、特にトリコット地が好ましい。 The woven or knitted fabric structure of the curtain woven or knitted fabric using the polyester fiber of the present invention is not particularly limited. Examples of the woven structure include plain weave, oblique weave (twill, twill), satin weave (satin), and the like. Any of these can be used. As the knitted fabric structure, any of a warp knitted tricot fabric, a russell fabric, a circular knitted fabric, a single circular knitted fabric, and a double circular knitted fabric can be used. The warp knitted fabric excellent in the thickness is preferable, and the tricot fabric is particularly preferable.
また、本発明のポリエステル繊維は、その清涼感、ハリコシ感、光沢感の特徴を活かすことにより、織編物のみならず、刺繍糸として使用することもできる。このように刺繍糸として使用する場合には、形態安定性の観点から沸騰水収縮率が5%以下であるものを使用することが好ましい。 Further, the polyester fiber of the present invention can be used not only as a woven or knitted fabric but also as an embroidery thread by making use of the characteristics of its refreshing feeling, firmness and glossiness. Thus, when using it as an embroidery thread, it is preferable to use the thing whose boiling water shrinkage rate is 5% or less from a viewpoint of form stability.
更に、本発明のポリエステル繊維は、その清涼感、ハリコシ感、光沢感の特徴を活かすことにより、インナー用途の織編物として使用することもできる。このインナー用途では十分な清涼感、ハリコシ感、光沢感を活かすことが可能である。 Furthermore, the polyester fiber of the present invention can also be used as a woven or knitted fabric for inner use by taking advantage of its coolness, elasticity, and glossiness. In this inner use, it is possible to make full use of a refreshing feeling, a firm feeling, and a glossy feeling.
以下、実施例により本発明を詳細に説明する。実施例中に使用した各特性値は次の測定方法により求めた。 Hereinafter, the present invention will be described in detail by way of examples. Each characteristic value used in the examples was determined by the following measurement method.
〔沸騰水収縮率〕
ポリエステル繊維をカセ取り機で10回巻き取り、0.09g/dtexの荷重を掛けて試長aを測定し、100℃の沸騰水中で15分間熱処理し、8時間以上自然乾燥した後0.09g/dtexの荷重を掛け、試長bを測定し、次の式より沸騰水収縮率を算出する。
沸騰水収縮率(%)=〔(a−b)/a〕×100
[Boiling water shrinkage]
The polyester fiber is wound 10 times with a casserole machine, the test length a is measured by applying a load of 0.09 g / dtex, heat-treated in boiling water at 100 ° C. for 15 minutes, and naturally dried for 8 hours or more and then 0.09 g A load of / dtex is applied, the test length b is measured, and the boiling water shrinkage is calculated from the following equation.
Boiling water shrinkage rate (%) = [(ab) / a] × 100
〔光沢度、風合い特性(光沢感)〕
試験糸を緯打ち込みした1/3ツイル織物を作成し、(株)村上色彩技術研究所製の自動変角光沢計(GP−200)を用い、条件「入射角45°、反射角45°」及び「入射角45°、反射角90°」で、最大値−最小値を光沢度として評価した。その際、酸化マグネシウム白板を光沢度50とした。
[Glossiness, texture characteristics (glossiness)]
A 1/3 twill woven fabric in which the test yarn was wefted was created, and the condition “incident angle 45 °, reflection angle 45 °” was measured using an automatic variable gloss meter (GP-200) manufactured by Murakami Color Research Laboratory Co., Ltd. In addition, the maximum value-minimum value was evaluated as the glossiness at an incident angle of 45 ° and a reflection angle of 90 °. At that time, the gloss of magnesium oxide white plate was set to 50.
また、同試験において、光沢感の品位を経験10年以上の検査員により評価し、「極めて優れている」は○○、「優れている」は○、「普通」は△、「劣っている」は×の4段階で評価した。なお、基準試料にはポリエチレンテレフタレート丸断面延伸糸84dtex−48filにより上記と同様に製織した織物を使用し、これを「劣っている:×」として評価した。 Also, in this test, the quality of glossiness was evaluated by an inspector with 10 years of experience or more. “Excellent” is ◯, “Excellent” is ◯, “Normal” is △, “Inferior” "" Was evaluated in 4 grades. A woven fabric woven in the same manner as described above with a polyethylene terephthalate round section drawn yarn 84dtex-48fil was used as a reference sample, and this was evaluated as "Inferior: x".
〔風合い特性(清涼感、ハリコシ感)〕
各項目とも、試料を基準試料との一対比較による官能試験を実施し、「極めて優れている」は○○、「優れている」は○、「普通」は△、「劣っている」は×の4段階で評価した。なお、基準試料には、ポリエチレンテレフタレート丸断面延伸糸84dtex−48filを使用して上記試料と同様に製織したものを用い、これを「劣っている:×」とした。
[Texture characteristics (coolness, harshness)]
For each item, the sample is subjected to a sensory test based on a paired comparison with the reference sample. “Excellent” is ○○, “Excellent” is ○, “Normal” is △, “Inferior” is × The four grades were evaluated. In addition, as a reference sample, what was woven in the same manner as the above sample using a polyethylene terephthalate round section drawn yarn 84dtex-48fil was used, and this was defined as "Inferior: x".
〔耐水圧〕
JIS−L−1092Aに基づく、耐水度試験方法(静水圧法)で測定した。なお、本発明の耐水圧の基準値は5.0kPa以上である。
(Water pressure resistance)
It measured by the water resistance test method (hydrostatic pressure method) based on JIS-L-1092A. In addition, the reference value of the water pressure resistance of the present invention is 5.0 kPa or more.
〔Lb値〕
以下に示す方法で織物を作製し、常法により染色、水洗、乾燥を行った。以上の方法で得た織物を用いて以下に示す方法でLb値の測定を行った。
[Lb value]
A woven fabric was prepared by the method described below, and dyeing, washing with water and drying were carried out by conventional methods. Using the fabric obtained by the above method, the Lb value was measured by the following method.
(1)製織方法
経糸に84dtex、36フィラメントの延伸糸を用い、緯糸に実施例、比較例で得 られた延伸糸を幅1.7m、織密度90本/25mm、織機回転数800cpmで打 ち込み、織物とする。
(2)Lb値測定方法。
(1) Weaving method Stretched yarns of 84 dtex and 36 filaments were used for the warp, and the stretched yarns obtained in the examples and comparative examples were weaved at a width of 1.7 m, a weaving density of 90 yarns / 25 mm, and a loom rotation speed of 800 cpm. And weaving.
(2) Lb value measurement method.
スガ試験機(株)製の測色計SM−3型を用い、測定サンプル設置部における黒さと 白さの確認を行う。黒さの確認は、測定部に黒色に染色されたフェルト布を取付け、 フェルト布のL値(明度)が14±0.5%であることを確認する。白さの確認は、測 定部に標準白板を取付け、標準白板のL値(明度)が91±0.5%であることを確認 する。これらの確認手順は、生地のL値(明度)を測定する通常法であり一般化されて いる方法である。白度の高い生地のL値は91%に近くなり、逆に黒い生地のL値は1 4%に近くなる。 Using a colorimeter SM-3 manufactured by Suga Test Instruments Co., Ltd., check the blackness and whiteness of the measurement sample installation area. To check the blackness, attach a felt cloth dyed in black to the measuring part and confirm that the L value (lightness) of the felt cloth is 14 ± 0.5%. To check the whiteness, attach a standard white plate to the measuring unit and check that the L value (brightness) of the standard white plate is 91 ± 0.5%. These confirmation procedures are the usual methods for measuring the L value (brightness) of fabrics and are generalized methods. The L value of a fabric with high whiteness is close to 91%, and conversely, the L value of a black fabric is close to 14%.
Lb値は、次式により算出する。ここで、LBは黒色フェルト布と評価サンプル1枚 を測定部に取付けて測定したL値、LWは標準白板と評価サンプル1枚を測定部に取 付 けて測定したL値である。なお、同一評価試料1枚で繰り返し5回測定し、その平 均値をLb値とする。
Lb=(LW−LB)
The Lb value is calculated by the following formula. Here, LB is an L value measured by attaching a black felt cloth and one evaluation sample to the measurement part, and LW is an L value measured by attaching a standard white board and one evaluation sample to the measurement part. Note that the same evaluation sample is repeatedly measured 5 times, and the average value is taken as the Lb value.
Lb = (LW−LB)
〔採光率(%)〕
以下に示す方法で織物を作製し、常法により染色、水洗、乾燥を行った。以上の方法で得た織物を用いて以下に示す方法で採光率の測定を行った。
[Lighting rate (%)]
A woven fabric was prepared by the following method, and dyed, washed with water and dried by a conventional method. Using the woven fabric obtained by the above method, the lighting rate was measured by the following method.
(1)製織方法
経糸に84dtex−36filの延伸糸を用い、緯糸に実施例、比較例で得られ た延伸糸を幅1.7m、織密度90本/25mm、織機回転数800cpmで打ち込 み、織物とする。
(2)採光率測定方法
レフランプ(1万ルックス)を照射した際の生地透過照度の比率を採光率(%)と する。
(1) Weaving method Using 84 dtex-36 fil drawn yarn as the warp, the drawn yarn obtained in the examples and comparative examples as wefts, driven at a width of 1.7 m, a weaving density of 90 pieces / 25 mm, and a loom rotation speed of 800 cpm. Suppose weaving.
(2) Daylighting rate measuring method The ratio of the fabric transmission illuminance when irradiated with a reflex lamp (10,000 lux) is taken as the daylighting rate (%).
実施例1〜3及び比較例1〜6
テレフタル酸ジメチル100部、エチレングリコール71部、酢酸カルシウム0.09部を150〜230℃に加熱して生成するメタノールを連続的に系外に除去しながら4.5hrエステル交換反応を行わせる。次いで亜リン酸およびトリメチルホスヘートを添加し、酸化アンチモン0.03部を添加して1時間で徐々に昇温して280℃にすると共に減圧して133Pa以下の真空度にする。280℃,133Pa以下の真空度で極限粘度が0.66になるまで重合させる。極限粘度の調節はかき混ぜ機のトルクを測定して行った。ポリマの極限粘度はo−クロロフェノール中で25℃で測定した。
Examples 1-3 and Comparative Examples 1-6
A transesterification reaction is carried out for 4.5 hr while continuously removing methanol produced by heating 100 parts of dimethyl terephthalate, 71 parts of ethylene glycol and 0.09 part of calcium acetate to 150 to 230 ° C. Next, phosphorous acid and trimethyl phosphate are added, 0.03 part of antimony oxide is added, and the temperature is gradually raised to 1 hour at 280 ° C. and the pressure is reduced to 133 Pa or less. Polymerization is performed at 280 ° C. and a vacuum of 133 Pa or less until the intrinsic viscosity becomes 0.66. The intrinsic viscosity was adjusted by measuring the torque of the agitator. The intrinsic viscosity of the polymer was measured in o-chlorophenol at 25 ° C.
得られたポリマをポリマをチップ状に切断し、180℃で5hr乾燥したポリエチレンテレフタレートを使用し、それぞれ扁平度、異形度I、異形度IIを異ならせるように紡糸速度3000m/分で引き取った後、延伸倍率1.72で延伸した。得られた延伸糸特性を表1に示す。 After the obtained polymer was cut into chips and polyethylene terephthalate dried at 180 ° C. for 5 hours was used, and after drawing at a spinning speed of 3000 m / min so as to have different flatness, irregularity I, and irregularity II, respectively. The film was stretched at a stretching ratio of 1.72. The obtained drawn yarn characteristics are shown in Table 1.
次いで、得られた延伸糸を経糸、緯糸に用いて、カバーファクターWCF=1500、FCF=990の高密度織物とし、得られた特性を表1に示す。 Next, the obtained drawn yarn was used for warp and weft to make a high-density fabric with a cover factor of WCF = 1500 and FCF = 990, and the obtained properties are shown in Table 1.
表1の結果から、実施例1〜3は、十分な断面形状、扁平度、異形度I、異形度II、単糸繊度を有することにより、耐水性があり、極めて優れた清涼感、ハリコシ感及び光沢感を有する高密度織物が得られた。これに対して比較例1〜6は、ハリコシ感が不十分であり、光沢感のないものであった。 From the result of Table 1, Examples 1-3 have water resistance by having sufficient cross-sectional shape, flatness, irregularity degree I, irregularity degree II, and single yarn fineness, and are very excellent refreshing feeling and harshness feeling. And a high-density fabric having a glossy feeling was obtained. On the other hand, Comparative Examples 1 to 6 had insufficient harshness and no glossiness.
実施例4、5及び比較例7、8
テレフタル酸ジメチル100部、エチレングリコール71部、酢酸カルシウム0.09部を150〜230℃に加熱して生成するメタノールを連続的に系外に除去しながら4.5hrエステル交換反応を行わせる。次いで亜リン酸およびトリメチルホスヘートを添加し、酸化アンチモン0.03部を添加して1時間で徐々に昇温して280℃にすると共に減圧して133Pa以下の真空度にする。ただし、比較例7のみ、他の添加物と同時に艶消し剤として酸化チタンを更に添加する。280℃,133Pa以下の真空度で極限粘度が0.66になるまで重合させる。極限粘度の調節はかき混ぜ機のトルクを測定して行った。ポリマの極限粘度はo−クロロフェノール中で25℃で測定した。
Examples 4 and 5 and Comparative Examples 7 and 8
A 4.5 hr transesterification reaction is carried out while continuously removing 100 parts of dimethyl terephthalate, 71 parts of ethylene glycol, and 0.09 part of calcium acetate to 150 to 230 ° C. and continuously removing methanol generated from the system. Next, phosphorous acid and trimethyl phosphate are added, 0.03 part of antimony oxide is added, and the temperature is gradually raised to 1 hour at 280 ° C. and the pressure is reduced to 133 Pa or less. However, only in Comparative Example 7, titanium oxide is further added as a matting agent simultaneously with other additives. Polymerization is performed at 280 ° C. and a vacuum of 133 Pa or less until the intrinsic viscosity becomes 0.66. The intrinsic viscosity was adjusted by measuring the torque of the agitator. The intrinsic viscosity of the polymer was measured in o-chlorophenol at 25 ° C.
得られたポリマをポリマをチップ状に切断し、180℃で5hr乾燥したポリエチレンテレフタレートを使用し、紡糸速度2800m/分で引き取った後、延伸倍率1.82で延伸した。得られた延伸糸を経糸、緯糸に用いて、カバーファクターWCF=1650、FCF=1050の高密度織物とし、得られた特性を表2に示す。 The obtained polymer was cut into chips and the polyethylene terephthalate dried at 180 ° C. for 5 hours was taken up at a spinning speed of 2800 m / min and then drawn at a draw ratio of 1.82. The obtained drawn yarn is used for warp and weft to form a high-density fabric with a cover factor of WCF = 1650 and FCF = 1050, and the properties obtained are shown in Table 2.
実施例4、5は、本発明に適した断面形状、扁平度、異形度I、異形度IIを有し、単糸繊度も適しているので耐水性があり、極めて優れたハリコシ感、光沢感を有し、優れた清涼感を有する高密度織物が得られた。これに対して比較例7、8は、耐水性がなく、粗硬感のある高密度織物となった。 Examples 4 and 5 have a cross-sectional shape, flatness, irregularity degree I, irregularity degree II suitable for the present invention, and single yarn fineness is also suitable, so that it has water resistance, extremely excellent feeling of firmness and glossiness. Thus, a high-density fabric having an excellent refreshing feeling was obtained. On the other hand, Comparative Examples 7 and 8 were high-density fabrics having no water resistance and a feeling of coarseness.
実施例6、7及び比較例9
テレフタル酸ジメチル100部、エチレングリコール71部、酢酸カルシウム0.09部を150〜230℃に加熱して生成するメタノールを連続的に系外に除去しながら4.5hrエステル交換反応を行わせる。次いで亜リン酸およびトリメチルホスヘートを添加し、酸化アンチモン0.03部を添加して1時間で徐々に昇温して280℃にすると共に減圧して133Pa以下の真空度にする。280℃,133Pa以下の真空度で極限粘度が0.66になるまで重合させる。極限粘度の調節はかき混ぜ機のトルクを測定して行った。ポリマの極限粘度はo−クロロフェノール中で25℃で測定した。
Examples 6 and 7 and Comparative Example 9
A 4.5 hr transesterification reaction is carried out while continuously removing 100 parts of dimethyl terephthalate, 71 parts of ethylene glycol, and 0.09 part of calcium acetate to 150 to 230 ° C. and continuously removing methanol generated from the system. Next, phosphorous acid and trimethyl phosphate are added, 0.03 part of antimony oxide is added, and the temperature is gradually raised to 1 hour at 280 ° C. and the pressure is reduced to 133 Pa or less. Polymerization is performed at 280 ° C. and a vacuum of 133 Pa or less until the intrinsic viscosity becomes 0.66. The intrinsic viscosity was adjusted by measuring the torque of the agitator. The intrinsic viscosity of the polymer was measured in o-chlorophenol at 25 ° C.
得られたポリマをポリマをチップ状に切断し、180℃で5hr乾燥したポリエチレンテレフタレートを使用し、それぞれ単糸繊度を異ならせて、紡糸速度3200m/分で引き取った後、延伸倍率1.68で延伸した。得られた延伸糸を経糸、緯糸に用いて、カバーファクターWCF=1450、FCF=870の高密度織物とし、得られた特性を表3に示す。 The obtained polymer was cut into chips and the polyethylene terephthalate dried at 180 ° C. for 5 hours was used, and each single yarn fineness was varied and taken at a spinning speed of 3200 m / min. Stretched. The obtained drawn yarn is used for warp and weft to form a high-density fabric with a cover factor of WCF = 1450 and FCF = 870, and the properties obtained are shown in Table 3.
実施例6、7は、本発明に適した断面形状、扁平度、異形度I、異形度IIを有し、単糸繊度も適しているので耐水性があり、極めて優れたハリコシ感、光沢感を有し、優れた清涼感を有する高密度織物が得られた。しかし、比較例9は、耐水性がなく、粗硬感のある高密度織物となった。 Examples 6 and 7 have a cross-sectional shape, flatness, irregularity degree I, irregularity degree II suitable for the present invention, and single yarn fineness is also suitable, so that they have water resistance, and extremely excellent harshness and glossiness. Thus, a high-density fabric having an excellent refreshing feeling was obtained. However, Comparative Example 9 was a high-density fabric having no water resistance and a feeling of coarseness.
実施例8、9
テレフタル酸ジメチル100部、エチレングリコール71部、酢酸カルシウム0.09部を150〜230℃に加熱して生成するメタノールを連続的に系外に除去しながら4.5hrエステル交換反応を行わせる。次いで亜リン酸およびトリメチルホスヘートを添加し、酸化アンチモン0.03部を添加して1時間で徐々に昇温して280℃にすると共に減圧して133Pa以下の真空度にする。280℃,133Pa以下の真空度で極限粘度が0.66になるまで重合させる。極限粘度の調節はかき混ぜ機のトルクを測定して行った。ポリマの極限粘度はo−クロロフェノール中で25℃で測定した。
Examples 8 and 9
A 4.5 hr transesterification reaction is carried out while continuously removing 100 parts of dimethyl terephthalate, 71 parts of ethylene glycol, and 0.09 part of calcium acetate to 150 to 230 ° C. and continuously removing methanol generated from the system. Next, phosphorous acid and trimethyl phosphate are added, 0.03 part of antimony oxide is added, and the temperature is gradually raised to 1 hour at 280 ° C. and the pressure is reduced to 133 Pa or less. Polymerization is performed at 280 ° C. and a vacuum of 133 Pa or less until the intrinsic viscosity becomes 0.66. The intrinsic viscosity was adjusted by measuring the torque of the agitator. The intrinsic viscosity of the polymer was measured in o-chlorophenol at 25 ° C.
得られたポリマをポリマをチップ状に切断し、180℃で5hr乾燥したポリエチレンテレフタレートを使用し、紡糸速度2800m/分で引き取った後、沸騰水収縮率を変更するような延伸条件で巻き取った。得られた延伸糸を経糸、緯糸に用いて、カバーファクターWCF=1700、FCF=1150の高密度織物とし、得られた織物の特性を表4に示す。 The obtained polymer was cut into chips and the polyethylene terephthalate dried at 180 ° C. for 5 hours was used and taken up at a spinning speed of 2800 m / min. Then, the polymer was wound up under stretching conditions that changed the boiling water shrinkage rate. . The obtained drawn yarn is used for warp and weft to make a high-density fabric with a cover factor of WCF = 1700 and FCF = 1150, and the properties of the obtained fabric are shown in Table 4.
実施例8は本発明に適した断面形状、扁平度、異形度I、異形度II、単糸繊度を有し、艶消し剤を含有しないので、優れた清涼感、ハリコシ感、光沢感及び耐水圧を有する高密度織物が得られた。 Example 8 has a cross-sectional shape suitable for the present invention, flatness, irregularity degree I, irregularity degree II, single yarn fineness, and does not contain a matting agent, so it has an excellent refreshing feeling, harshness feeling, glossiness, and resistance to resistance. A high density fabric with water pressure was obtained.
実施例9は、本発明に適した断面形状、扁平度、異形度I、異形度II、単糸繊度を有し、艶消し剤を含有しないので、優れた清涼感、ハリコシ感、光沢感を有するが、沸騰水収縮率がやや高いので耐水圧のやや低い高密度織物であった。 Example 9 has a cross-sectional shape suitable for the present invention, flatness, irregularity degree I, irregularity degree II, single yarn fineness, and does not contain a matting agent, so it has excellent refreshing feeling, harshness feeling, and glossiness. Although it has a boiling water shrinkage rate, it was a high-density fabric with a slightly low water pressure resistance.
実施例10〜12及び比較例10〜15
前述した実施例1〜3で製造したポリエステル繊維と繊度構成だけを表5に示すように異ならせるように製造したポリエステル繊維を使用して、上記に記載の製織方法よりカーテン用織物を製織した。得られた織物の特性を表5に示す。
Examples 10-12 and Comparative Examples 10-15
A curtain fabric was woven by the weaving method described above using the polyester fiber manufactured in Examples 1 to 3 and the polyester fiber manufactured so that only the fineness configuration was different as shown in Table 5. The properties of the resulting fabric are shown in Table 5.
表5の結果から、実施例10〜12は、十分な断面形状、扁平度、異形度I、異形度II、単糸繊度を有することにより、遮像性、採光性があり、極めて優れた清涼感、ハリコシ感及び光沢感を有するカーテン用織物が得られた。これに対して比較例10〜15は、ハリコシ感が不十分であり、光沢感のないものであった。 From the results of Table 5, Examples 10 to 12 have sufficient cross-sectional shape, flatness, irregularity degree I, irregularity degree II, and single yarn fineness, so that they have image-shielding properties and daylighting properties, and are extremely excellent in cooling. A curtain fabric having a feeling, a firm feeling and a glossy feeling was obtained. On the other hand, Comparative Examples 10 to 15 had insufficient elasticity and no glossiness.
実施例13,14及び比較例16,17
前述した実施例4,5で製造したポリエステル繊維と繊度構成だけを表6に示すように異ならせるように製造したポリエステル繊維を使用して、上記に記載の製織方法よりカーテン用織物を製織した。得られた織物の特性を表6に示す。
Examples 13 and 14 and Comparative Examples 16 and 17
The curtain fabric was woven by the weaving method described above using the polyester fibers manufactured in Examples 4 and 5 and the polyester fibers manufactured so that only the fineness configuration was different as shown in Table 6. The properties of the resulting fabric are shown in Table 6.
実施例13,14は、本発明に適した断面形状、扁平度、異形度I、異形度IIを有し、単糸繊度も適しているので遮像性、採光性があり、極めて優れたハリコシ感、光沢感を有し、優れた清涼感を有するカーテン用織物が得られた。これに対して比較例16,17は、遮像性、採光性がなく、粗硬感のあるカーテン用織物となった。 Examples 13 and 14 have a cross-sectional shape, flatness, irregularity degree I, irregularity degree II suitable for the present invention, and single yarn fineness is also suitable, so that they have image-shielding properties and daylighting properties, and are extremely excellent in elasticity. A curtain fabric having a feeling of sensation and gloss and an excellent refreshing feeling was obtained. On the other hand, Comparative Examples 16 and 17 were curtain fabrics that had no image-shielding properties and no daylighting properties and had a rough feeling.
実施例15,16及び比較例18
前述した実施例6,7で製造したポリエステル繊維と繊度構成だけを表7に示すように異ならせるように製造したポリエステル繊維を使用して、上記に記載の製織方法よりカーテン用織物を製織した。得られた織物の特性を表7に示す。
得られた延伸糸を上記製織方法よりカーテン用織物とし、得られた特性を表3に示す。
Examples 15 and 16 and Comparative Example 18
A curtain fabric was woven by the weaving method described above using the polyester fibers manufactured in Examples 6 and 7 and the polyester fibers manufactured so that only the fineness configuration was different as shown in Table 7. The properties of the resulting fabric are shown in Table 7.
The obtained drawn yarn was made into a curtain fabric by the above weaving method, and the obtained properties are shown in Table 3.
実施例15,16は、本発明に適した断面形状、扁平度、異形度I、異形度IIを有し、単糸繊度も適しているので遮像性、採光性があり、極めて優れたハリコシ感、光沢感を有し、優れた清涼感を有するカーテン用織物が得られた。しかし、比較例18は、遮像性、採光性がなく、粗硬感のあるカーテン用織物となった。 Examples 15 and 16 have a cross-sectional shape, flatness, irregularity degree I, irregularity degree II suitable for the present invention, and single yarn fineness is also suitable, so that there are image-shielding properties and daylighting properties, and extremely excellent elasticity. A curtain fabric having a feeling of sensation and gloss and an excellent refreshing feeling was obtained. However, Comparative Example 18 was a curtain fabric having no image-blocking property and daylighting property and having a rough and hard feeling.
実施例17,18
前述した実施例8,9で製造したポリエステル繊維と繊度構成だけを表8に示すように異ならせるように製造したポリエステル繊維を使用して、上記に記載の製織方法よりカーテン用織物を製織した。得られた織物の特性を表8に示す。
Examples 17 and 18
The curtain fabric was woven by the weaving method described above using the polyester fibers manufactured in Examples 8 and 9 described above and the polyester fibers manufactured so that only the fineness configuration was different as shown in Table 8. The properties of the resulting fabric are shown in Table 8.
実施例17は本発明に適した断面形状、扁平度、異形度I、異形度II、単糸繊度を有し、艶消し剤を含有しないので、優れた清涼感、ハリコシ感、光沢感及び遮像性、採光性を有するカーテン用織物が得られた。 Example 17 has a cross-sectional shape suitable for the present invention, flatness, irregularity degree I, irregularity degree II, single yarn fineness, and does not contain a matting agent, so that it has an excellent refreshing feeling, sharp feeling, glossiness and shading. A curtain fabric having image properties and daylighting properties was obtained.
実施例18は、本発明に適した断面形状、扁平度、異形度I、異形度II、単糸繊度を有し、艶消し剤を含有しないので、優れた清涼感、ハリコシ感、光沢感を有するが、沸騰水収縮率がやや高いので遮像性、採光性のやや低いカーテン用織物であった。 Example 18 has a cross-sectional shape suitable for the present invention, flatness, irregularity degree I, irregularity degree II, single yarn fineness, and does not contain a matting agent, so it has an excellent refreshing feeling, harshness feeling and glossiness. Although it has a boiling water shrinkage rate, it is a fabric for curtains having a slightly low image-shielding property and daylighting property.
1 紡糸パック
2 紡糸口金
3 冷却チムニー
4 給油ガイド
5 インターレースノズル
6 引取ローラー
7 パッケージ
1
Claims (11)
扁平度(A/B)=1.2〜2.2
異形度I(C/D)=1.1〜1.3
異形度II(B/D)=1.1〜1.6
A>B≧C>D The single fiber fineness is 2.5 dtex or less, and the single fiber cross-sectional shape is a flat multilobal shape having six to ten leaves, and the longest major axis connecting the vertices of the circumscribed circle of the flat multilobal shape is A and the major axis A Among the short diameters that are perpendicular to each other and connect the apexes of the convex portions of the flat multilobal shape, B is the largest short diameter, C is the shortest diameter that is the same or the second longest short diameter B, and the flat multileaf shape. Polyester consisting of a single fiber satisfying the following formula, where D is the shortest short diameter of the short diameters connecting the bottoms of the recesses, and the glossiness of the single fiber is 35 to 70 fiber.
Flatness (A / B) = 1.2 to 2.2
Deformation degree I (C / D) = 1.1 to 1.3
Deformation degree II (B / D) = 1.1 to 1.6
A> B ≧ C> D
11. The polyester fiber woven or knitted fabric for curtain according to claim 10, wherein the density of the woven or knitted fabric is 60 to 100 pieces / 25 mm in the case of a woven fabric, and 30 to 60 courses / 25 mm in the case of a knitted fabric.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004151304A JP2005350777A (en) | 2003-05-22 | 2004-05-21 | Polyester fiber |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003144831 | 2003-05-22 | ||
| JP2004139657 | 2004-05-10 | ||
| JP2004151304A JP2005350777A (en) | 2003-05-22 | 2004-05-21 | Polyester fiber |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2005350777A true JP2005350777A (en) | 2005-12-22 |
Family
ID=35585487
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004151304A Pending JP2005350777A (en) | 2003-05-22 | 2004-05-21 | Polyester fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2005350777A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007327161A (en) * | 2006-06-09 | 2007-12-20 | Teijin Fibers Ltd | Woven fabric excellent in ultraviolet-shielding ability, air permeability and gloss, and clothing using the same |
| JP2008081863A (en) * | 2006-09-26 | 2008-04-10 | Toray Ind Inc | Polyester fiber and fabric having anti-see-through property and water absorbency |
| JP2009209501A (en) * | 2008-03-06 | 2009-09-17 | Teijin Fibers Ltd | Non-visible loop pile woven fabric and interior article |
| WO2014132690A1 (en) * | 2013-02-26 | 2014-09-04 | 東レ株式会社 | Nonwoven fabric |
| US20150052871A1 (en) * | 2013-08-21 | 2015-02-26 | Nippon Pillar Packing Co., Ltd. | Yarn |
| CN105051275A (en) * | 2013-03-27 | 2015-11-11 | 东丽株式会社 | Spun yarn and woven or knitted fabric |
| WO2016027493A1 (en) * | 2014-08-20 | 2016-02-25 | 東レ株式会社 | Non-woven fabric for sanitary materials, and sanitary material product |
| WO2016068279A1 (en) * | 2014-10-31 | 2016-05-06 | 東レ株式会社 | Fiber structure for use as cell scaffold material |
| JP2016138352A (en) * | 2015-01-28 | 2016-08-04 | 東レ株式会社 | Long / short composite spun yarn |
| JP2021070897A (en) * | 2019-10-24 | 2021-05-06 | アクトインテリア株式会社 | Super water-absorbing quick-drying resin fiber, nonwoven fabric and method for producing super water-absorbing quick-drying resin fiber |
-
2004
- 2004-05-21 JP JP2004151304A patent/JP2005350777A/en active Pending
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007327161A (en) * | 2006-06-09 | 2007-12-20 | Teijin Fibers Ltd | Woven fabric excellent in ultraviolet-shielding ability, air permeability and gloss, and clothing using the same |
| JP2008081863A (en) * | 2006-09-26 | 2008-04-10 | Toray Ind Inc | Polyester fiber and fabric having anti-see-through property and water absorbency |
| JP2009209501A (en) * | 2008-03-06 | 2009-09-17 | Teijin Fibers Ltd | Non-visible loop pile woven fabric and interior article |
| CN105074074B (en) * | 2013-02-26 | 2018-01-02 | 东丽株式会社 | Non-woven fabrics |
| CN105074074A (en) * | 2013-02-26 | 2015-11-18 | 东丽株式会社 | Nonwoven fabric |
| JPWO2014132690A1 (en) * | 2013-02-26 | 2017-02-02 | 東レ株式会社 | Non-woven |
| WO2014132690A1 (en) * | 2013-02-26 | 2014-09-04 | 東レ株式会社 | Nonwoven fabric |
| EP2963168A4 (en) * | 2013-02-26 | 2016-09-21 | Toray Industries | NONWOVEN FABRIC |
| CN105051275A (en) * | 2013-03-27 | 2015-11-11 | 东丽株式会社 | Spun yarn and woven or knitted fabric |
| CN105051275B (en) * | 2013-03-27 | 2018-02-13 | 东丽株式会社 | Spinning and braid |
| EP2980288A4 (en) * | 2013-03-27 | 2016-12-07 | Toray Industries | WOVEN AND KNITTED YARN AND TEXTILE |
| US20150052871A1 (en) * | 2013-08-21 | 2015-02-26 | Nippon Pillar Packing Co., Ltd. | Yarn |
| CN104420038A (en) * | 2013-08-21 | 2015-03-18 | 日本皮拉工业株式会社 | Yarn |
| JPWO2016027493A1 (en) * | 2014-08-20 | 2017-06-29 | 東レ株式会社 | Non-woven fabric for hygiene materials and hygiene material products |
| CN106661790A (en) * | 2014-08-20 | 2017-05-10 | 东丽株式会社 | Non-woven fabric for sanitary materials, and sanitary material product |
| WO2016027493A1 (en) * | 2014-08-20 | 2016-02-25 | 東レ株式会社 | Non-woven fabric for sanitary materials, and sanitary material product |
| EP3184681A4 (en) * | 2014-08-20 | 2018-02-28 | Toray Industries, Inc. | Non-woven fabric for sanitary materials, and sanitary material product |
| CN106661790B (en) * | 2014-08-20 | 2019-05-28 | 东丽株式会社 | Hygienic material non-woven fabrics and hygienic material product |
| JPWO2016068279A1 (en) * | 2014-10-31 | 2017-08-10 | 東レ株式会社 | Fiber structure as cell scaffold material |
| CN107109335A (en) * | 2014-10-31 | 2017-08-29 | 东丽株式会社 | Fiber construct as cell scaffold material |
| WO2016068279A1 (en) * | 2014-10-31 | 2016-05-06 | 東レ株式会社 | Fiber structure for use as cell scaffold material |
| JP2016138352A (en) * | 2015-01-28 | 2016-08-04 | 東レ株式会社 | Long / short composite spun yarn |
| JP2021070897A (en) * | 2019-10-24 | 2021-05-06 | アクトインテリア株式会社 | Super water-absorbing quick-drying resin fiber, nonwoven fabric and method for producing super water-absorbing quick-drying resin fiber |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5612702B2 (en) | Textiles and clothing | |
| CN104947282A (en) | Thin woven fabric | |
| JP2005350777A (en) | Polyester fiber | |
| JP5297331B2 (en) | Core-sheath type composite fiber | |
| WO2004057074A1 (en) | Polyester false-twisted yarn and method of manufacturing the yarn | |
| JP5777391B2 (en) | Interior interior materials | |
| JP2002105796A (en) | Shading fabric | |
| KR101590231B1 (en) | Polyester multi-filament fiber with twisted yarn effect and method for manufacturing thereof | |
| JP2000282344A (en) | Ultraviolet screening fabric | |
| JPS5920775B2 (en) | Consensusinoseizohouhou | |
| JP5324360B2 (en) | Fabrics and textile products including core-sheath type composite false twisted yarn | |
| JP2018150629A (en) | Knitted fabric knitted with composite textured yarn | |
| JPH0359130A (en) | Polyester blended yarn having different shrinkage | |
| JP4700238B2 (en) | Polyester false twisted yarn and method for producing the same | |
| JPS6189320A (en) | Polyester thick and thin yarn and its production | |
| JPH04136217A (en) | Elliptical uneven cross-sectional polyester fiber | |
| JPH08218247A (en) | Opaque fiber aggregate | |
| JP3863051B2 (en) | Polyester spotted yarn | |
| JP3333831B2 (en) | Polyester thick yarn | |
| JP2559684B2 (en) | Cashmere fabric and method for producing the same | |
| JP2012012726A (en) | Heat-shielding woven or knitted fabric and clothing | |
| JP4395948B2 (en) | Low shrinkage polyester yarn and polyester blended yarn comprising the same | |
| JP2011162888A (en) | Polyester blended yarn and polyester fabric | |
| JP2008081861A (en) | Method for producing polyester combined filament yarn | |
| JP2702128B2 (en) | Pile yarn for napping fabric |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070427 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20090807 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20090811 |
|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20091007 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20091027 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20100302 |
