JP2005240208A - Polyester combined filament yarn having small fineness and method for producing the same - Google Patents
Polyester combined filament yarn having small fineness and method for producing the same Download PDFInfo
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- JP2005240208A JP2005240208A JP2004049174A JP2004049174A JP2005240208A JP 2005240208 A JP2005240208 A JP 2005240208A JP 2004049174 A JP2004049174 A JP 2004049174A JP 2004049174 A JP2004049174 A JP 2004049174A JP 2005240208 A JP2005240208 A JP 2005240208A
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- 229920000728 polyester Polymers 0.000 title claims abstract description 48
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000009835 boiling Methods 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 238000009987 spinning Methods 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 2
- 208000012886 Vertigo Diseases 0.000 description 11
- 238000000034 method Methods 0.000 description 8
- 239000000155 melt Substances 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- -1 polyethylene terephthalate Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical group C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
- UUAGPGQUHZVJBQ-UHFFFAOYSA-N Bisphenol A bis(2-hydroxyethyl)ether Chemical compound C=1C=C(OCCO)C=CC=1C(C)(C)C1=CC=C(OCCO)C=C1 UUAGPGQUHZVJBQ-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
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- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
Abstract
Description
本発明は、繊度が100dtex以下と細繊度であっても、高い強度を有しながら優れた風合を呈する細繊度ポリエステル混繊糸およびその製造方法に関するものである。 The present invention relates to a fine polyester blended yarn that exhibits excellent texture while having high strength even when the fineness is 100 dtex or less and a method for producing the same.
従来、多種多様のポリエステル混繊糸が多種提案されており、様々な用途で利用されている。一方、スポーツ織物などの用途では、引裂強力向上などの観点から高強力の糸が使用されており、通常ポリエステルの固有粘度を高くして糸のシルクファクターを向上させる方法が採用されている(特許文献1参照)。 Conventionally, a wide variety of polyester blend yarns have been proposed and used in various applications. On the other hand, high-strength yarns are used in sports fabrics and other applications from the standpoint of improving tear strength, and a method of increasing the silk factor of the yarn by increasing the intrinsic viscosity of polyester is generally used (patented) Reference 1).
このような知見から、固有粘度で高いポリエステルを用いた高強力の糸が主として芯部を占め、鞘部に物性の異なる糸が配置されるような混繊糸であれば、高強力でかつループによる嵩高性などの性能の発現が期待できることは容易に予想される。しかし、こうした混繊糸の強力は、主として芯糸の物性で決定されるため、鞘糸を混ぜることにより混繊糸の繊度あたりの強度は低下するという問題があるだけでなく、薄地の織物用として用いる場合には糸の細さが不十分であるという問題がある。 From these findings, high-strength yarns using high-strength yarns with high intrinsic viscosity are mainly high-strength and loops if they are mixed yarns where yarns with different physical properties occupy the core part and the sheath part has different physical properties. It is easily expected that performance such as bulkiness can be expected. However, the strength of these mixed yarns is mainly determined by the physical properties of the core yarn, so there is not only the problem that the strength per fineness of the mixed yarn decreases by mixing the sheath yarn, but also for thin fabrics. When used as a thread, there is a problem that the yarn is not fine enough.
このような問題を改善するためには、鞘部に配される糸の比率を低下させる必要があり、そのためには鞘糸に使用する糸を細くする必要がある。しかしながら、例えば30dtex以下の細い糸は、擦過による糸切れなどが頻発しやすいため、安定して生産することは困難である。 In order to improve such a problem, it is necessary to reduce the ratio of the thread | yarn distribute | arranged to a sheath part, For that purpose, it is necessary to make the thread | yarn used for a sheath thread | yarn thin. However, for example, a thin thread of 30 dtex or less is difficult to stably produce because thread breakage due to abrasion is likely to occur frequently.
このような問題を解消する方法としては、例えば特許文献2に提案されているように、同一又は異なる紡糸口金から芯糸となる成分と鞘糸となる成分とを同時に紡糸し、これを混繊交絡処理した後に延伸加工等の後加工を施す方法がある。しかしながら、本発明者らの研究によれば、一方成分として固有粘度の高いポリエステルを使用する場合には、溶融粘度の関係で紡糸温度を高くする必要があり、その結果、他方のポリエステルの劣化が大きくなって安定に紡糸できなくなるという問題がある。 As a method for solving such a problem, for example, as proposed in Patent Document 2, a component that becomes a core yarn and a component that becomes a sheath yarn are simultaneously spun from the same or different spinneret, and this is mixed. There is a method of performing post-processing such as stretching after the entanglement treatment. However, according to the study by the present inventors, when a polyester having a high intrinsic viscosity is used as one component, it is necessary to increase the spinning temperature in relation to the melt viscosity, and as a result, the other polyester is deteriorated. There is a problem that it becomes large and cannot be stably spun.
本発明は、上記背景技術を鑑みなされたもので、その目的は、細繊度であっても、高い強度を有しながら優れた外観を呈するポリエステル混繊糸を提供することにある。 The present invention has been made in view of the above-described background art, and an object of the present invention is to provide a polyester mixed yarn that exhibits an excellent appearance while having high strength even if it has a fineness.
本発明者らの研究によれば、上記課題は、「固有粘度が0.75〜1.00、5%伸長時の応力が1.5〜2.4cN/dtex、沸水収縮率が6〜15%、単糸繊度が1.0〜5.0dtexであるポリエステルフィラメントAと、固有粘度が0.5〜0.65、5%伸長時の応力が1.0cN/dtex以下、沸水収縮率が6%以下、単糸繊度が1.0〜5.0dtexであるポリエステルフィラメントBとから構成される紡糸混繊糸であって、該ポリエステルフィラメントBの混繊糸全重量を基準とする割合が5〜30重量%であり、且つ混繊糸の総繊度が30〜100dtex、強度が4.5〜7.0cN/dtex、交絡数が3〜10ケ/mであることを特徴とする細繊度ポリエステル混繊糸。」により達成できることが見出された。 According to the study by the present inventors, the above-mentioned problem is as follows: “Intrinsic viscosity is 0.75 to 1.00, stress at 5% elongation is 1.5 to 2.4 cN / dtex, boiling water shrinkage is 6 to 15 %, Polyester filament A having a single yarn fineness of 1.0 to 5.0 dtex, intrinsic viscosity of 0.5 to 0.65, stress at 5% elongation of 1.0 cN / dtex or less, boiling water shrinkage of 6 % Or less, a spun mixed yarn composed of a polyester filament B having a single yarn fineness of 1.0 to 5.0 dtex, wherein the ratio based on the total weight of the blended yarn of the polyester filament B is 5 to 5%. 30% by weight, the total fineness of the blended yarn is 30 to 100 dtex, the strength is 4.5 to 7.0 cN / dtex, and the number of entanglements is 3 to 10 / m 2 It was found that it can be achieved by “fiber yarn.” .
また、このようなポリエステル混繊糸は、「同一の紡糸パック内であって互いに異なる紡糸口金から互いに異なる固有粘度のポリエステルを溶融吐出し、該吐出糸条を冷却固化後に集束して混繊交絡処理した後に未延伸糸として引取り、次いで延伸熱処理する製造方法において、紡糸パック内に送液するポリエステルの温度を、固有粘度が高い方のポリエステルが低い方のポリエステルよりも5℃以上高くなるようにすることを特徴とする細繊度ポリエステル混繊糸の製造方法。」により製造できることが見出された。 Further, such a polyester blended yarn is described as follows: “Polyesters having different intrinsic viscosities are melted and discharged from different spinnerets in the same spin pack, and the discharged yarns are converged after cooling and solidification to be mixed and entangled. In the manufacturing method in which the polyester is fed as an undrawn yarn after the treatment and then drawn and heat-treated, the temperature of the polyester fed into the spin pack is higher by 5 ° C. or more than the polyester having the higher intrinsic viscosity than the polyester having the lower intrinsic viscosity. It has been found that it can be produced by a method for producing a polyester fine fiber yarn having a fineness characterized in that it is characterized by:
本発明の細繊度ポリエステル混繊糸は、固有粘度が高くて高強力高弾性の高収縮糸と、固有粘度が低い低弾性の低収縮糸とを紡糸の段階で混繊しているので、低収縮成分の割合を少なくしても優れた外観を呈し、強度と外観を両立させることができる。 The fineness polyester blended yarn of the present invention has a high intrinsic viscosity, high strength and high elasticity, high shrinkage yarn and low elasticity, low elasticity, low shrinkage yarn, which are mixed at the spinning stage. Even if the ratio of the shrinking component is reduced, an excellent appearance can be obtained, and both strength and appearance can be achieved.
本発明におけるポリエステルは、主たる繰返し単位がエチレンテレフタレートであるポリエステルを主たる対象とし、他の成分を全酸成分を基準として15モル%以下、好ましくは10モル%以下、特に好ましくは5モル%以下の割合で共重合したものであってもよい。好ましく用いられる共重合成分としては、イソフタル酸、フタル酸、アジピン酸、セバシン酸、5−ナトリウムスルホイソフタル酸、テトラメチレングリコール、トリメチレングリコール、ジエチレングリコール、ネオペンチルグリコール、ビスフェノールA、2,2−ビス(4−ヒドロキシエトキシフェニル)プロパンなどがあげられる。 The polyester in the present invention is mainly a polyester whose main repeating unit is ethylene terephthalate, and other components are 15 mol% or less, preferably 10 mol% or less, particularly preferably 5 mol% or less based on the total acid components. It may be copolymerized in proportion. Preferred copolymerization components include isophthalic acid, phthalic acid, adipic acid, sebacic acid, 5-sodium sulfoisophthalic acid, tetramethylene glycol, trimethylene glycol, diethylene glycol, neopentyl glycol, bisphenol A, 2,2-bis (4-hydroxyethoxyphenyl) propane and the like.
本発明のポリエステル混繊糸を構成している一方成分のフィラメントAは、その固有粘度が0.75〜1.00、5%伸長時の応力が1.5〜2.4cN/dtex、沸水収縮率が6〜15%、単糸繊度が1.0〜5.0dtexである必要がある。 The filament A as one component constituting the polyester mixed yarn of the present invention has an intrinsic viscosity of 0.75 to 1.00, a stress at 5% elongation of 1.5 to 2.4 cN / dtex, and boiling water shrinkage. It is necessary that the rate is 6 to 15% and the single yarn fineness is 1.0 to 5.0 dtex.
該フィラメントAの固有粘度は、混繊糸に十分な強力と破断耐性(シルクファクター)を得るために前記範囲とする必要がある。なお、この値が0.75未満の場合には、他方成分である後述するフィラメントBとの差が小さくなりすぎて、嵩高性も発現しがたくなるので好ましくない。一方、1.00を越える場合には、そのようなフィラメントを製糸することが極めて難しくなり、商業的に生産することが困難になる。より好ましい固有粘度の範囲は0.90〜1.00である。 The intrinsic viscosity of the filament A needs to be in the above range in order to obtain sufficient strength and breaking resistance (silk factor) for the mixed yarn. In addition, when this value is less than 0.75, since the difference with the filament B mentioned later which is the other component becomes too small, and bulkiness becomes difficult to express, it is not preferable. On the other hand, when it exceeds 1.00, it becomes very difficult to produce such a filament, and it becomes difficult to produce commercially. A more preferable range of intrinsic viscosity is 0.90 to 1.00.
また、5%伸長時の応力が1.5cN/dtex未満または沸水収縮率が6%未満の場合には、後述するフィラメントBとの物性差が小さくなりすぎ、やはり嵩高性が発現しがたくなる。逆に5%伸長時の応力が2.4cN/dtexを越える場合には、そのようなフィラメントを製糸することが極めて困難になり、沸水収縮率が15%を越える場合には、収縮が大きすぎるために風合が低下するので好ましくない。 Further, when the stress at 5% elongation is less than 1.5 cN / dtex or the boiling water shrinkage rate is less than 6%, the difference in physical properties from the filament B described later becomes too small, and the bulkiness is hardly exhibited. . Conversely, when the stress at 5% elongation exceeds 2.4 cN / dtex, it becomes very difficult to produce such a filament, and when the boiling water shrinkage rate exceeds 15%, the shrinkage is too large. For this reason, the texture is lowered, which is not preferable.
次に単糸繊度が1.0dtex未満の場合には、製糸時に糸切れが多発するようになるので好ましくなく、逆に5.0dtexを越える場合には風合が粗硬になるので好ましくない。 Next, when the single yarn fineness is less than 1.0 dtex, it is not preferable because yarn breakage frequently occurs at the time of yarn production. On the contrary, when it exceeds 5.0 dtex, the texture becomes coarse and hard.
次に本発明のポリエステル混繊糸を構成している他方成分のフィラメントBは、その固有粘度が0.50〜0.65、5%伸長時の応力が1.0cN/dtex以下、沸水収縮率が6%以下、単糸繊度が1.0〜5.0dtexである必要がある。 Next, the other component filament B constituting the polyester mixed yarn of the present invention has an intrinsic viscosity of 0.50 to 0.65, a stress at 5% elongation of 1.0 cN / dtex or less, and a boiling water shrinkage. Must be 6% or less, and the single yarn fineness should be 1.0 to 5.0 dtex.
該フィラメントBの固有粘度が0.5未満の場合には、紡糸時の融液の粘度が低下しすぎるため、安定に紡糸することが困難になる。一方、0.65を超える場合には、フィラメントAとの差が小さくなり、やはり嵩高性が発現しがたくなる。 When the intrinsic viscosity of the filament B is less than 0.5, the viscosity of the melt at the time of spinning is too low, and it becomes difficult to spin stably. On the other hand, when it exceeds 0.65, the difference from the filament A becomes small, and the bulkiness is hardly exhibited.
また、5%伸長時の応力が1.0cN/dtexを越える場合または沸水収縮率が6%を越える場合には、戦術のフィラメントAとの差が小さくなりすぎるため、嵩高性が発現しがたくなる。さらに単糸繊度が1.0dtex未満の場合には、製糸時に糸切れが多発するようになり、逆に5.0dtexを越える場合には風合が粗硬になるので好ましくない。 Also, when the stress at 5% elongation exceeds 1.0 cN / dtex or the boiling water shrinkage rate exceeds 6%, the difference from the tactic filament A becomes too small, so that the bulkiness is hardly exhibited. Become. Furthermore, when the single yarn fineness is less than 1.0 dtex, yarn breakage frequently occurs during yarn production, and conversely, when it exceeds 5.0 dtex, the texture becomes coarse, which is not preferable.
上記のフィラメントAとフィラメントBとからなる本発明の混繊糸は、その総繊度が30〜100dtex、好ましくは50〜90dtexの範囲にあり、かつ、フィラメントBの混繊糸全重量を基準とする割合が5〜30重量%、好ましくは10〜25重量%特に好ましくは15〜20重量%の範囲にある必要がある。総繊度が30dtex未満の場合には糸自体の強度が不十分となって糸切れしやすくなり、安定に生産することが困難になる。一方100dtexを越える場合には、織物などの布帛とした際、柔軟性や布帛の薄さが悪化するので好ましくない。また、フィラメントBの割合が5重量%未満の場合には外観が低下し、逆に30重量%を越える場合にはフィラメントAの割合が低下して混繊糸としての強度が低下するので本発明の目的を達成できなくなる。 The mixed yarn of the present invention comprising the filament A and the filament B has a total fineness of 30 to 100 dtex, preferably 50 to 90 dtex, and is based on the total weight of the mixed yarn of the filament B. The proportion should be in the range of 5-30% by weight, preferably 10-25% by weight, particularly preferably 15-20% by weight. When the total fineness is less than 30 dtex, the strength of the yarn itself is insufficient, the yarn is easily broken, and stable production becomes difficult. On the other hand, when it exceeds 100 dtex, the flexibility and the thinness of the fabric are deteriorated when a fabric such as a woven fabric is used. Further, when the ratio of the filament B is less than 5% by weight, the appearance is deteriorated. Conversely, when the ratio is more than 30% by weight, the ratio of the filament A is decreased and the strength as a mixed yarn is decreased. The purpose of can not be achieved.
さらに本発明の混繊糸は、その強度が4.5〜7.0cN/dtexの範囲にある必要がある。該強度が4.5cN/dtex未満の場合には、強度が通常の混繊糸と同等で不十分であり、本発明の目的を達成することができない。一方7.0cN/dtexを越える場合には、製糸時に糸切れが多発し、このような混繊糸を安定に生産することが困難となる。 Furthermore, the mixed yarn of the present invention needs to have a strength in the range of 4.5 to 7.0 cN / dtex. When the strength is less than 4.5 cN / dtex, the strength is equivalent to that of a normal mixed yarn and is insufficient, and the object of the present invention cannot be achieved. On the other hand, when it exceeds 7.0 cN / dtex, yarn breakage occurs frequently during yarn making, and it is difficult to stably produce such a mixed yarn.
また本発明の混繊糸は、交絡数3〜10ケ/mの交絡を有している必要がある。該交絡数がこの範囲未満の場合には、製糸における延伸時にフィラメントAとフィラメントBとが分離しやすく、安定に延伸処理することが困難になる。一方交絡数が10ケ/mを越える場合には、熱処理してもフィラメントBがループ状に十分張出すことができず風合が低下するので好ましくない。 Moreover, the mixed yarn of this invention needs to have the entanglement of 3-10 entanglements / m. When the number of entanglements is less than this range, the filament A and the filament B are easily separated at the time of drawing in the yarn making, and it becomes difficult to perform the drawing process stably. On the other hand, if the number of entanglements exceeds 10 m / m, the filament B cannot be sufficiently stretched out in a loop shape even after heat treatment, and the feeling is lowered, which is not preferable.
以上に説明した本発明の混繊糸は、例えば以下の方法により容易に製造することができる。すなわち、互いに固有粘度が異なるポリエステルを、固有粘度が高い方のポリエステルの温度が、固有粘度が低い方のポリエステルの温度よりも5℃以上高くなるように加熱溶融し、それぞれのポリマー流を計量して紡糸パックに送液し、次いで同一の紡糸パック内にあって互いに異なる紡糸口金から、好ましくは高固有粘度ポリエステルの温度と同じ温度で溶融吐出する。 The mixed fiber of the present invention described above can be easily manufactured by, for example, the following method. That is, polyesters having different intrinsic viscosities are heated and melted so that the temperature of the polyester having the higher intrinsic viscosity is 5 ° C. or more higher than the temperature of the polyester having the lower intrinsic viscosity, and each polymer stream is measured. Then, the solution is fed to a spinning pack, and then melt-discharged from different spinnerets in the same spinning pack, preferably at the same temperature as that of the high intrinsic viscosity polyester.
ここで、両ポリマーの温度差が5℃未満の場合には、高固有粘度のポリエステルの溶融粘度が高くなりすぎて送液性が低下して安定に紡糸することができなくなるか、または低固有粘度ポリエステルの溶融粘度が低くなりすぎるか若しくは熱劣化して安定に紡糸することができなくなるので好ましくない。なお、低固有粘度ポリエステルの紡糸パック平均滞留時間は2分以下とするのが、ポリマーの熱分解抑制の点から好ましい。 Here, when the temperature difference between the two polymers is less than 5 ° C., the melt viscosity of the polyester having a high intrinsic viscosity becomes too high and the liquid feeding property is lowered, so that stable spinning cannot be performed, or the low intrinsic viscosity is low. Viscosity polyester is not preferable because the melt viscosity becomes too low or heat degradation causes stable spinning. In addition, it is preferable from the point of suppression of thermal decomposition of a polymer that the spinning pack average residence time of low intrinsic viscosity polyester shall be 2 minutes or less.
溶融吐出された糸条は、冷却風を吹付けて冷却固化後に集束し、次いで例えばインターレースノズルなどの流体処理装置を通過させて交絡を付与した後、500〜2500m/分、好ましくは800〜1500m/分の速度で引取る。この際、使用するポリエステルの固有粘度は、最終的に得られるフィラメントAおよびBの固有粘度が前記範囲となるものを用いる。また、交絡数が3〜10個/mとなるように流体処理装置を選択するか、流体処理条件(例えば空気圧)を適宜選択設定する。 The melted and discharged yarn is focused after cooling and solidification by blowing cooling air, and then passed through a fluid processing device such as an interlace nozzle, and then entangled to give 500 to 2500 m / min, preferably 800 to 1500 m. Take up at the rate of / min. At this time, the intrinsic viscosity of the polyester to be used is such that the intrinsic viscosity of the filaments A and B finally obtained is in the above range. In addition, the fluid processing apparatus is selected so that the number of entanglements is 3 to 10 / m, or fluid processing conditions (for example, air pressure) are appropriately selected and set.
交絡処理された未延伸糸は、従来公知の方法により、前記特性を満足する混繊糸となるよう、温度70〜100℃、好ましくは80〜95℃で、2.5〜4.5倍、好ましくは3.0〜4.0倍に延伸後、温度180〜220℃で熱セットする。 The undrawn yarn subjected to the entanglement treatment is a temperature of 70 to 100 ° C., preferably 80 to 95 ° C., 2.5 to 4.5 times, so as to be a mixed yarn satisfying the above properties by a conventionally known method. Preferably, the film is heat-set at a temperature of 180 to 220 ° C. after stretching to 3.0 to 4.0 times.
以下、実施例をあげて本発明をさらに具体的に説明する。
[実施例1]
固有粘度が0.95のポリエチレンテレフタレートと固有粘度が0.64のポリエチレンテレフタレートとを、図1に示す2成分ポリマーの同時紡糸が可能な設備を用い、それぞれを表1記載の温度で押出機にて溶融後、紡糸パックに融液を供給した。その際、高固有粘度側:低固有粘度側の吐出重量比が8:2となるようにし、かつ延伸後の総繊度が78dtexとなるように計量後、温度295℃の紡糸口金より吐出した。吐出された糸条は、冷却後インターレースノズルにて交絡数10ケ/mとなるように交絡処理を施し、1000m/分の速度にて巻き取った。
Hereinafter, the present invention will be described more specifically with reference to examples.
[Example 1]
Using the equipment capable of simultaneously spinning polyethylene terephthalate with an intrinsic viscosity of 0.95 and polyethylene terephthalate with an intrinsic viscosity of 0.64 as shown in FIG. After melting, the melt was supplied to the spin pack. At that time, after the measurement was performed so that the discharge weight ratio of the high intrinsic viscosity side to the low intrinsic viscosity side was 8: 2, and the total fineness after drawing was 78 dtex, the mixture was discharged from a spinneret at a temperature of 295 ° C. The discharged yarn was entangled with an interlace nozzle after cooling so that the number of entanglement was 10 / m and wound at a speed of 1000 m / min.
得られた未延伸糸を温度95℃で3.36倍に延伸し、次いで温度200℃で熱セットを施し表1記載の混繊糸を得た。得られた混繊糸の評価結果を表1に示す。 The obtained undrawn yarn was drawn 3.36 times at a temperature of 95 ° C., and then heat-set at a temperature of 200 ° C. to obtain mixed yarns described in Table 1. Table 1 shows the evaluation results of the obtained mixed yarn.
なお、フィラメントAおよびBの単糸物性は、それぞれ20本のフィラメントを分離して測定をおこなった。また、固有粘度は、o−クロロフェノールを溶媒として温度35℃で測定した。 The single yarn physical properties of filaments A and B were measured by separating 20 filaments from each other. The intrinsic viscosity was measured at a temperature of 35 ° C. using o-chlorophenol as a solvent.
[実施例2]
実施例1において、高固有粘度側のポリエステルの溶融温度を293℃とし、表2記載の条件で紡糸延伸する以外は実施例1と同様にした。得られた混繊糸の評価結果を表2に示す。なお、ポリエステルの溶融粘度が高くなりすぎて紡糸安定性は低下した。
[Example 2]
In Example 1, the same procedure as in Example 1 was followed, except that the high intrinsic viscosity polyester had a melting temperature of 293 ° C. and was spun and stretched under the conditions shown in Table 2. Table 2 shows the evaluation results of the obtained mixed yarn. In addition, the melt viscosity of the polyester became too high, and the spinning stability was lowered.
本発明のポリエステル混繊糸は紡糸混繊法により製造されたものなので、細繊度の混繊糸でありながら強度と外観が両立したものを安定に製糸することができ、品位に優れた布帛などの最終製品を提供することができる。 Since the polyester blended yarn of the present invention is produced by the spinning blending method, it is possible to stably produce a blended yarn having a fineness and having both strength and appearance, excellent in quality, etc. Can provide the final product.
1 芯側ポリマー計量ギアポンプ.
2 鞘側ポリマー計量ギアポンプ
3 ポリマー供給ブロック
4 紡糸パック
5 紡糸口金
1 Core side polymer metering gear pump.
2 Sheath side polymer metering gear pump 3 Polymer supply block 4
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Citations (4)
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JPS6189319A (en) * | 1984-10-03 | 1986-05-07 | Toray Ind Inc | Production of polyester mixed fiber with thermal-shrinkage difference |
JPS6342913A (en) * | 1986-08-11 | 1988-02-24 | Kuraray Co Ltd | Production of combined filament yarn of different shrinkage |
JPH08144145A (en) * | 1994-11-21 | 1996-06-04 | Kuraray Co Ltd | Polyester differently shrinkable blended yarn |
JP2002054023A (en) * | 2000-08-01 | 2002-02-19 | Teijin Ltd | Method of producing polyester multi-shrinkable mixed filament yarn |
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JPS6189319A (en) * | 1984-10-03 | 1986-05-07 | Toray Ind Inc | Production of polyester mixed fiber with thermal-shrinkage difference |
JPS6342913A (en) * | 1986-08-11 | 1988-02-24 | Kuraray Co Ltd | Production of combined filament yarn of different shrinkage |
JPH08144145A (en) * | 1994-11-21 | 1996-06-04 | Kuraray Co Ltd | Polyester differently shrinkable blended yarn |
JP2002054023A (en) * | 2000-08-01 | 2002-02-19 | Teijin Ltd | Method of producing polyester multi-shrinkable mixed filament yarn |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102677188A (en) * | 2012-06-04 | 2012-09-19 | 浙江理工大学 | Traverse mechanisms of silk reeling machine and with first-order degeneration eccentric-circle gear and second-order conjugate non-circular gear |
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