TW202340557A - Polyamide multifilament and fabric - Google Patents

Polyamide multifilament and fabric Download PDF

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TW202340557A
TW202340557A TW112101485A TW112101485A TW202340557A TW 202340557 A TW202340557 A TW 202340557A TW 112101485 A TW112101485 A TW 112101485A TW 112101485 A TW112101485 A TW 112101485A TW 202340557 A TW202340557 A TW 202340557A
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polyamide
multifilament
yarn
fabric
inorganic particles
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TW112101485A
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Chinese (zh)
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岸田泰輔
兼田千奈美
渡邊雄大
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日商東麗股份有限公司
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    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/60Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/90Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyamides
    • DTEXTILES; PAPER
    • D03WEAVING
    • D03DWOVEN FABRICS; METHODS OF WEAVING; LOOMS
    • D03D15/00Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
    • D03D15/20Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads
    • D03D15/283Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads synthetic polymer-based, e.g. polyamide or polyester fibres

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Artificial Filaments (AREA)

Abstract

This polyamide multifilament has a single fiber fineness of 2.2 dtex or less, results in not more than one fluff or slack existing per 10000 m of the multifilament, provides a dynamic friction coefficient of 0.8 [mu]d or less between a metal and a yarn, and has an aliphatic hydrocarbon chain having a carbon number of C7 or more between amide bonds.

Description

聚醯胺複絲及織物Polyamide multifilament and fabrics

本發明係關於在醯胺鍵間具碳數C7以上之脂肪族烴鏈的聚醯胺複絲。若將本發明的聚醯胺複絲使用於織物,便可提供低通氣性、品質、及高階步驟順暢性優異的織物。The present invention relates to polyamide multifilaments having aliphatic hydrocarbon chains with a carbon number of C7 or more between the amide bonds. If the polyamide multifilament of the present invention is used in fabrics, fabrics with excellent low air permeability, quality, and smoothness in advanced steps can be provided.

屬於合成纖維的聚醯胺纖維,因為具有獨特的柔軟度、高強度、染色時發色性、耐熱性、吸濕性等優異特性,因而廣泛使用於內衣著、戶外夾克等衣料用途。Polyamide fiber, a synthetic fiber, is widely used in underwear, outdoor jackets and other clothing applications because of its unique softness, high strength, color development when dyed, heat resistance, moisture absorption and other excellent properties.

近年因為對建設永續社會的意識高漲,去石油化原料的活動逐漸活躍化,就連聚醯胺纖維亦要求非石化原料化。使用非石化原料的聚醯胺樹脂,已知有將篦麻使用為起始原料的聚醯胺410、聚醯胺510、聚醯胺610、聚醯胺612、聚醯胺1010、聚醯胺11等,任一者均係單體單元具有長鏈碳鏈的結構。In recent years, due to the rising awareness of building a sustainable society, activities to eliminate petrochemical raw materials have become increasingly active. Even polyamide fibers are required to be made of non-petrochemical raw materials. Polyamide resins using non-petrochemical raw materials include polyamide 410, polyamide 510, polyamide 610, polyamide 612, polyamide 1010, and polyamide using castrate as a starting material. 11 and so on, any one of them has a structure in which the monomer unit has a long carbon chain.

另一方面,在例如屬於領導去石油化原料活動的戶外服飾之核心商品的戶外夾克、羽絨外套用途中,從防風、防羽絨脫落的觀點,要求織物的低通氣性,因而要求將纖維細纖度化並複絲化。On the other hand, for applications such as outdoor jackets and down jackets, which are core products of outdoor apparel that are leading the movement to eliminate petrochemical raw materials, fabrics are required to have low air permeability from the viewpoint of wind protection and down shedding prevention, so the fiber fineness is required to be reduced. and multifilamentation.

單體單元具有長鏈碳鏈的聚醯胺之製絲技術,例如專利文獻1,藉由將在製絲時的聚合物水分率適當化便可調整黏度,俾能提供延伸時毛球品質良好的聚醯胺610複絲。 [先前技術文獻] [專利文獻] The yarn-making technology of polyamides whose monomer units have long carbon chains, such as Patent Document 1, can adjust the viscosity by appropriately adjusting the moisture content of the polymer during yarn-making, so as to provide good quality pills during stretching. Polyamide 610 multifilament. [Prior technical literature] [Patent Document]

[專利文獻1]國際公開第2019/163971號[Patent Document 1] International Publication No. 2019/163971

(發明所欲解決之問題)(The problem that the invention wants to solve)

然而,專利文獻1所記載之方法,係以漁網為代表的產業用途為對象,且以單絲纖度達4.8dtex以上與衣料用途對比為較粗纖度的纖維為對象者。主要泛用於衣料用途的單絲細纖度物,仍有會產生毛球的課題。又,高階加工的步驟順暢性亦差,進行織物時會有條痕等製品品質差的課題。However, the method described in Patent Document 1 is targeted at industrial uses such as fishing nets, and is targeted at fibers with a single filament fineness of 4.8 dtex or more, which is relatively coarse in comparison with clothing applications. Monofilament fine-density fabrics, which are mainly used for clothing, still have the problem of producing pills. In addition, the smoothness of high-end processing steps is also poor, and there are issues such as streaks when fabricating and poor product quality.

本發明係為解決上述課題而完成,在於提供:能提供高階加工的步驟順暢性優異、低通氣性、製品品質優異織物的聚醯胺複絲。 (解決問題之技術手段) The present invention was completed to solve the above-mentioned problems, and aims to provide a polyamide multifilament yarn that can provide fabrics with excellent smoothness in high-end processing steps, low air permeability, and excellent product quality. (Technical means to solve problems)

為解決上述課題,本發明為以下構成。 (1)一種聚醯胺複絲,其係單絲纖度為2.2dtex以下、每10000m的毛球鬆垮個數在1個以下、絲-金屬間的動摩擦係數為0.8μd以下,且醯胺鍵間具有碳數C7以上的脂肪族烴鏈。 (2)如上述(1)所記載的聚醯胺複絲,其中,含有無機粒子0.01~5.0質量%。 (3)一種織物,其係其中一部分含有(1)或(2)所記載的聚醯胺複絲。 (對照先前技術之功效) In order to solve the above-mentioned problems, the present invention has the following configuration. (1) A polyamide multifilament with a single filament fineness of 2.2 dtex or less, a loose ball number of less than 1 per 10,000 m, a filament-metal dynamic friction coefficient of 0.8 μd or less, and an amide bond. There is an aliphatic hydrocarbon chain with a carbon number of C7 or above. (2) The polyamide multifilament yarn according to the above (1), which contains 0.01 to 5.0% by mass of inorganic particles. (3) A fabric, a part of which contains the polyamide multifilament according to (1) or (2). (Compare the effectiveness of previous technologies)

藉由本發明的聚醯胺複絲,可提供:毛球與鬆垮(羽毛鬆垮)的產生受抑制、高階步驟順暢性優異,且低通氣性、製品品質優異,適用於戶外夾克等的織物。The polyamide multifilament of the present invention can provide fabrics that suppress the occurrence of pilling and looseness (loose feathers), have excellent smoothness in advanced steps, have low air permeability, and have excellent product quality, and are suitable for outdoor jackets, etc. .

[聚醯胺複絲] 本發明的聚醯胺複絲係單絲纖度在2.2dtex以下、每10000m的毛球鬆垮個數在1個以下、絲-金屬間之動摩擦係數在0.8μd以下,且醯胺鍵間具有碳數C7以上之脂肪族烴鏈的聚醯胺複絲。 [Polyamide multifilament] The fineness of the polyamide multifilament monofilament of the present invention is less than 2.2 dtex, the number of loose hair balls per 10,000 m is less than 1, the dynamic friction coefficient between silk and metal is less than 0.8 μd, and there is carbon between the amide bonds. Polyamide multifilament with aliphatic hydrocarbon chains of C7 or above.

(聚醯胺) 構成本發明之聚醯胺複絲的聚醯胺,係醯胺鍵間具有碳數(以下簡稱「C」)達7以上之脂肪族烴鏈的聚醯胺。 (polyamide) The polyamide constituting the polyamide multifilament of the present invention is a polyamide having an aliphatic hydrocarbon chain with a carbon number (hereinafter referred to as "C") of 7 or more between the amide bonds.

醯胺鍵間所含的碳數(即,亞甲基數),若以胺基羧酸、環狀醯胺為原料進行縮聚反應而製造的聚醯胺係為C9以上,若以二羧酸與二胺為原料進行縮聚反應而製造的聚醯胺則為C7以上。以胺基羧酸、環狀醯胺為原料進行縮聚反應而製造的聚醯胺、及以二羧酸與二胺為原料進行縮聚反應而製造的聚醯胺之碳數上限,均較佳為C12左右。The number of carbons (i.e., the number of methylene groups) contained between the amide bonds is C9 or more if the polyamide system is produced by polycondensation reaction using aminocarboxylic acid or cyclic amide as raw materials. The polyamide produced by polycondensation reaction with diamine as raw material is C7 or above. The upper limit of the carbon number of polyamides produced by polycondensation reaction of aminocarboxylic acid and cyclic amide as raw materials, and of polyamides produced by polycondensation reaction of dicarboxylic acid and diamine as raw materials is preferably: Around C12.

作為醯胺鍵間具有C7以上之脂肪族烴鏈的聚醯胺,以環狀醯胺為原料的聚醯胺有聚醯胺11,而以二羧酸與二胺為原料的聚醯胺有聚醯胺410、聚醯胺510、聚醯胺610、聚醯胺612、聚醯胺1010等。As a polyamide with an aliphatic hydrocarbon chain of C7 or above between the amide bonds, the polyamide using cyclic amide as raw material is polyamide 11, and the polyamide using dicarboxylic acid and diamine as raw material is Polyamide 410, polyamide 510, polyamide 610, polyamide 612, polyamide 1010, etc.

以下,將構成該等聚醯胺的原料之最小單元統括稱為「單體」。單體係可舉例如:源自石油的單體、源自生質的單體、源自石油的單體與源自生質的單體之混合物等。Hereinafter, the smallest unit of the raw materials constituting these polyamides is collectively referred to as "monomer". Examples of the monomer system include a petroleum-derived monomer, a biomass-derived monomer, a mixture of a petroleum-derived monomer and a biomass-derived monomer, and the like.

如前述,石油資源枯竭與地球暖化被視為問題,依世界性規模針對環境問題努力尋求方案,期待開發出使用未依存於石油資源且顧及環境之原料的製品。由此觀點,較佳係原料中含有源自生質的單體,更佳係單體中50質量%以上為利用生質獲得的單體。該源自生質的單體單元,較佳係50質量%以上、更佳係100質量%。As mentioned above, the depletion of petroleum resources and global warming are regarded as problems, and efforts are being made to find solutions to environmental problems on a global scale. It is expected to develop products that use raw materials that are not dependent on petroleum resources and are environmentally friendly. From this point of view, it is preferable that the raw material contains monomers derived from biomass, and more preferably 50% by mass or more of the monomers are monomers obtained by utilizing biomass. The monomer unit derived from biomass is preferably 50% by mass or more, and more preferably 100% by mass.

另外,源自生質的原料之驗證方法,係可例如:根據ASTM D6866法(20-B)利用放射性碳分析評價生物基碳濃度的方法。生物基碳濃度較佳係達50%以上、更佳係100%。In addition, the verification method of biomass-derived raw materials can be, for example, a method of evaluating bio-based carbon concentration using radiocarbon analysis according to ASTM D6866 method (20-B). The best bio-based carbon concentration is more than 50%, and the best is 100%.

如前述,在例如屬於領導去石油化原料活動的戶外服飾之核心商品的戶外夾克、羽絨外套用途中,從防風、防羽絨脫落的觀點,要求織物低通氣性,朝聚醯胺複絲的單絲細纖度化、高複絲化演進。As mentioned above, in applications such as outdoor jackets and down jackets, which are core products of outdoor apparel leading the movement to eliminate petrochemical raw materials, fabrics are required to have low air permeability from the viewpoint of windproofing and preventing down shedding, and there is a trend toward single polyamide multifilament yarns. The evolution of silk fineness and high multifilament.

(單絲纖度) 本發明的聚醯胺複絲係單絲纖度在2.2dtex以下,就實現戶外夾克、羽絨外套用織物的低通氣性而言係重要。較佳係1.3dtex以下。當較2.2dtex粗的情況,織物的通氣度高,對戶外夾克用途、羽絨外套用途所要求的數值而言較差。另一方面,隨單絲細纖度化,單絲強力會降低,因而容易產生毛球、鬆垮。毛球與鬆垮在製織步驟中會勾住筘等導致斷絲增加、或因張力變動而誘發條痕、斑點等缺陷的可能性。單絲纖度較佳係0.2dtex以上。 (monofilament fineness) The polyamide multifilament monofilament of the present invention has a fineness of 2.2 dtex or less, which is important in achieving low air permeability of fabrics for outdoor jackets and down jackets. The best one is below 1.3dtex. When it is thicker than 2.2 dtex, the breathability of the fabric is high, which is poor for the values required for outdoor jackets and down jackets. On the other hand, as the fineness of the monofilament becomes smaller, the strength of the monofilament decreases, making it easier to produce pilling and looseness. Hair balls and looseness may catch on the reed during the weaving process, leading to increased yarn breakage, or the possibility of inducing defects such as streaks and spots due to tension changes. The best single fiber fineness is above 0.2dtex.

(毛球鬆垮) 本發明的聚醯胺複絲係利用雷射式毛球檢測器所測定,每10000m的毛球鬆垮個數在1個以下。藉由設在該範圍內,便可使高階步驟順暢性、製品品質優異。若毛球鬆垮個數多於1個/10000m,則高階步驟順暢性、製品品質較差。 (The hair ball is loose) The polyamide multifilament of the present invention is measured using a laser-type pill detector. The number of loose pills per 10,000 m is less than 1. By setting it within this range, high-level steps can be made smooth and product quality can be excellent. If the number of loose hair balls is more than 1/10000m, the smoothness of the advanced steps and the quality of the product will be poor.

(儲存彈性模數、動摩擦係數) 特別係本發明所使用具有C7以上之脂肪族烴鏈的聚醯胺,相較於衣料用所使用之通用聚醯胺的聚醯胺6、聚醯胺66(具C6脂肪族烴鏈的聚醯胺),容易產生毛球鬆垮,但產生機制尚未明確。 (Storage elastic modulus, dynamic friction coefficient) In particular, the polyamide with an aliphatic hydrocarbon chain of C7 or above used in the present invention is compared with the general polyamides used in clothing materials such as polyamide 6 and polyamide 66 (polyamide with C6 aliphatic hydrocarbon chain). amide), it is easy to cause loose hair balls, but the mechanism is not yet clear.

本發明者等針對毛球鬆垮的產生機制進行深入鑽研。具C7以上之脂肪族烴鏈的聚醯胺,在纖維製造時的溫度範圍(常溫~80℃)中,相較於具C6以下之脂肪族烴鏈的聚醯胺,具有儲存彈性模數較低的性質,得知運行複絲(Running microfilament)與導絲器間之動摩擦係數提高。The inventors of the present invention conducted in-depth research on the mechanism of hair ball looseness. Polyamides with aliphatic hydrocarbon chains of C7 or above have a lower storage elastic modulus than polyamides with aliphatic hydrocarbon chains of C6 or below in the temperature range during fiber production (normal temperature ~ 80°C). The low properties indicate that the dynamic friction coefficient between the running microfilament and the yarn guide increases.

即,藉由醯胺鍵間具有C7以上的脂肪族烴鏈,每相同質量的醯胺鍵數降低,導致分子間氫鍵力降低。所以,成為具有不易引發聚醯胺結晶化、儲存彈性模數降低而容易變形之性質的聚醯胺。藉此,具有C7以上之脂肪族烴鏈的聚醯胺複絲,因與導絲器間之接觸、或因撓曲所生成之外力而容易變形,導致與導絲器間之接觸面積增加,而提高動摩擦係數,造成毛球鬆垮容易產生。That is, by having a C7 or higher aliphatic hydrocarbon chain between amide bonds, the number of amide bonds per the same mass decreases, resulting in a decrease in intermolecular hydrogen bonding force. Therefore, the polyamide has the properties of being less likely to cause crystallization of the polyamide, lowering the storage elastic modulus, and easily deforming. As a result, the polyamide multifilament yarn having a C7 or higher aliphatic hydrocarbon chain is easily deformed due to contact with the yarn guide or external force generated by deflection, resulting in an increase in the contact area with the yarn guide. Increasing the dynamic friction coefficient will easily cause loose hair balls.

具C7以上之脂肪族烴鏈的聚醯胺複絲,在纖維製造時容易受複絲與導絲器間之摩擦的影響,導致毛球鬆垮容易產生。又,不僅纖維製造時,就連高階加工步驟時亦同樣地會因複絲與導絲器間之摩擦而遭損傷。此種傾向係單絲纖度越細的複絲越明顯。Polyamide multifilaments with aliphatic hydrocarbon chains of C7 or above are easily affected by friction between the multifilament and the yarn guide during fiber manufacturing, resulting in loose hair balls. In addition, not only fiber manufacturing, but also high-level processing steps may be damaged due to friction between the multifilament and the yarn guide. This tendency is more obvious for multifilaments with finer single-filament fineness.

另外,此處所謂「儲存彈性模數」係利用動態黏彈性自動測定器(Rheovibron)測定獲得,考量複絲通過導絲器時的絲溫度,依50℃與80℃等2水準進行評價。In addition, the so-called "storage elastic modulus" here is measured using a dynamic viscoelasticity automatic measuring device (Rheovibron). The yarn temperature when the multifilament passes through the yarn guide is taken into consideration, and the evaluation is carried out at two levels: 50°C and 80°C.

本發明的聚醯胺複絲係絲-金屬間之動摩擦係數在0.8μd以下。此處所謂「動摩擦係數」係利用運行絲(Running yarn)摩擦係數測定裝置測定獲得,使用導絲器材質為鍍金屬鉻且經施行鏡面加工的金屬擦拭體,針對該金屬擦拭體與複絲間之動摩擦係數進行評價。後續將在實施例中敘述具體的測定方法。The dynamic friction coefficient between the polyamide multifilament yarn and the metal is below 0.8 μd. The so-called "dynamic friction coefficient" here is measured using a running yarn friction coefficient measuring device. The yarn guide material is a metal wiping body that is plated with metallic chromium and has a mirror finish. The friction between the metal wiping body and the multifilament yarn is measured. The dynamic friction coefficient is evaluated. Specific measurement methods will be described later in the Examples.

藉由將絲-金屬間的動摩擦係數設在0.8μd以下,便可減輕因複絲與導絲器間之摩擦所造成損傷,俾能使高階步驟順暢性、製品品質優異。若絲-金屬間的動摩擦係數高於0.8μd,則在製織時會因複絲與導絲器間之摩擦導致變形損傷產生,而誘發斷絲、毛球,造成高階步驟順暢性、製品品質變差。較佳的絲-金屬間之動摩擦係數係在0.7μd以下。By setting the dynamic friction coefficient between the wire and the metal below 0.8μd, the damage caused by the friction between the multifilament and the wire guide can be reduced, so that the high-end steps can be smooth and the product quality can be excellent. If the dynamic friction coefficient between the wire and the metal is higher than 0.8μd, deformation damage will occur due to the friction between the multifilament and the wire guide during weaving, which will induce wire breakage and hair balls, resulting in changes in the smoothness of high-level steps and product quality. Difference. The preferred dynamic friction coefficient between wire and metal is below 0.7μd.

為將本發明之聚醯胺複絲的動摩擦係數設在該範圍內,雖有各種途徑,但較佳為在纖維表面上形成微細凹凸。藉由纖維表面的微細凹凸,便可減少與導絲器間之接觸面積,便可控制動摩擦係數。In order to set the dynamic friction coefficient of the polyamide multifilament yarn of the present invention within this range, there are various methods, but it is preferable to form fine unevenness on the fiber surface. Through the fine unevenness on the fiber surface, the contact area with the yarn guide can be reduced, and the dynamic friction coefficient can be controlled.

(無機粒子) 為在纖維表面上形成微細凹凸,可在纖維製造時添加無機粒子。選擇無機粒子時,在屬於不會對纖維製造時造成不良影響、能保持纖維物性、且不致使聚合物出現著色等的無機粒子前提下,其餘並無特別的限定。無機粒子可舉例如:硫酸鋇、氧化鈦、氧化鋁、氧化鋯、氧化鈣、氧化鎂、氮化鋁、氮化硼、氮化鋯、矽酸鋁、碳化鋯等。該等無機粒子中,若考量纖維物性、發色性、粒子處置容易性、以及高階加工性,較佳係硫酸鋇、氧化鈦、氧化鎂、氧化鋁。 (Inorganic particles) In order to form fine unevenness on the fiber surface, inorganic particles can be added during fiber production. When selecting inorganic particles, there are no special restrictions as long as they are inorganic particles that do not cause adverse effects during fiber production, maintain fiber physical properties, and do not cause coloring of the polymer. Examples of inorganic particles include barium sulfate, titanium oxide, aluminum oxide, zirconium oxide, calcium oxide, magnesium oxide, aluminum nitride, boron nitride, zirconium nitride, aluminum silicate, zirconium carbide, and the like. Among these inorganic particles, in consideration of fiber physical properties, color development properties, ease of particle handling, and high-level processability, barium sulfate, titanium oxide, magnesium oxide, and aluminum oxide are preferred.

無機粒子含量係只要依動摩擦係數成為該範圍內的方式適當調整便可,若過多,則製絲性、屬於纖維物性的拉伸強度會降低,故較佳係0.01~5.0質量%。藉由含有0.01質量%以上,則在纖維表面上形成微細凹凸部,降低絲-金屬間之動摩擦係數而可減少毛球鬆垮產生,使高階步驟順暢性、製品品質優異。又,藉由設為5.0質量%以下,則不會阻礙纖維的配向・結晶化,可維持耐久性,且能減少單絲毛球,故高階步驟順暢性、製品品質優異。更佳係0.02~4.0質量%。The inorganic particle content can be appropriately adjusted so that the kinetic friction coefficient falls within this range. If it is too high, spinning properties and tensile strength, which are fiber physical properties, will decrease, so it is preferably 0.01 to 5.0 mass %. By containing 0.01% by mass or more, fine uneven portions are formed on the fiber surface, reducing the dynamic friction coefficient between the wire and the metal, thereby reducing the occurrence of loose hair balls, making high-end steps smooth and product quality excellent. In addition, by setting the content to 5.0 mass% or less, fiber orientation and crystallization are not hindered, durability can be maintained, and single filament pilling can be reduced, so high-end steps are smooth and product quality is excellent. More preferably, it is 0.02~4.0% by mass.

(纖度) 本發明的聚醯胺複絲因為係假設使用於衣料用途,因而總纖度較佳係156dtex以下、更佳係78dtex以下。 (denier) Since the polyamide multifilament yarn of the present invention is assumed to be used for clothing, the total fineness is preferably 156 dtex or less, more preferably 78 dtex or less.

(強度) 本發明的聚醯胺複絲因為係假設使用於衣料用途,因而強度較佳係3.0cN/dtex以上。藉由設在該範圍內,衣料的耐久性便可達到能承受實際使用的水準。 (strength) Since the polyamide multifilament yarn of the present invention is assumed to be used for clothing, the strength is preferably 3.0 cN/dtex or more. By setting it within this range, the durability of the clothing material can reach a level that can withstand actual use.

(伸度) 本發明的聚醯胺複絲因為係假設使用於衣料用途,因而伸度較佳係30~70%。藉由設在該範圍內,便可提供高階加工時的順暢性、且品質亦優異的衣料。相較於高配向未延伸絲,延伸絲的伸度較低,會有容易產生毛球鬆垮的傾向。將動摩擦係數控制在0.8μd以下的延伸絲(即伸度為30~50%的情況),可更加顯現抑制毛球鬆垮產生的效果。 (extension) Since the polyamide multifilament yarn of the present invention is expected to be used for clothing, the elongation is preferably 30 to 70%. By setting it within this range, it is possible to provide fabrics with excellent quality and smoothness during high-end processing. Compared with highly oriented unstretched yarns, stretched yarns have lower elongation, which tends to cause loose hair balls. The effect of controlling the dynamic friction coefficient below 0.8μd (that is, when the elongation is 30~50%) can further demonstrate the effect of suppressing the loosening of hair balls.

(硫酸相對黏度) 本發明的聚醯胺複絲因為係假設使用於衣料用途,因而聚醯胺的硫酸相對黏度較佳係1.7~3.5。藉由設在該範圍內,便可獲得上述強度與伸度的聚醯胺複絲,能提供衣料耐久性成為可承受實際使用的水準,且高階加工時的順暢性、品質亦優異的衣料。 (relative viscosity of sulfuric acid) Since the polyamide multifilament of the present invention is expected to be used for clothing, the sulfuric acid relative viscosity of the polyamide is preferably 1.7 to 3.5. By setting it within this range, the polyamide multifilament yarn with the above-mentioned strength and elongation can be obtained, and the durability of the clothing can be increased to a level that can withstand actual use, and the smoothness and quality of the clothing during high-end processing can also be excellent.

(纖維截面形狀) 本發明之聚醯胺複絲的單絲之纖維截面形狀並無特別的限定,可為例如:圓截面、偏平截面、透鏡形截面、多葉片截面、中空截面、以及其他公知的不同形狀截面。 (fiber cross-section shape) The fiber cross-sectional shape of the polyamide multifilament monofilament of the present invention is not particularly limited, and can be, for example, circular cross-section, flat cross-section, lens-shaped cross-section, multi-blade cross-section, hollow cross-section, and other well-known cross-sections of different shapes.

(無機粒子的長邊灰分量變動) 本發明的聚醯胺複絲在纖維長邊方向上任意10處所測定的灰分量之CV值,較佳係0.5以下。此處所謂「灰分」係指根據JIS L1013(2010)灰分所測定的值,CV值係變動的指標。針對在纖維長邊方向上任意10處取樣的纖維試料,計算出灰分量平均值與標準偏差,而求得CV值。 CV值(%)=(標準偏差)/(平均值)×100 藉由設在該範圍內,均勻的無機粒子便在纖維表面上形成微細凹凸,有助於將動摩擦係數與毛球個數設在該範圍。 (Changes in the ash content of the long sides of inorganic particles) The CV value of the ash content of the polyamide multifilament of the present invention measured at any 10 locations in the fiber longitudinal direction is preferably 0.5 or less. The "ash content" here refers to the value measured according to JIS L1013 (2010) ash content, and the CV value is an indicator of fluctuation. For fiber samples sampled at any 10 locations along the fiber length direction, the average and standard deviation of the ash content are calculated to obtain the CV value. CV value (%)=(standard deviation)/(mean)×100 By setting it within this range, uniform inorganic particles form fine irregularities on the fiber surface, which helps to set the dynamic friction coefficient and the number of hair balls within this range.

特別係本發明所使用具C7以上之脂肪族烴鏈的聚醯胺,相較於衣料用所採用通用聚醯胺的聚醯胺6、聚醯胺66(具C6脂肪族烴鏈的聚醯胺),無機粒子的分散性較差。理由係具有C7以上之脂肪族碳烴鏈的聚醯胺,藉由降低醯胺鍵的密度,使聚合物成為低極性,因與高極性無機粒子間之界面張力差變大,導致無機粒子的凝聚惡化所致。依此,因聚醯胺聚合物中的無機粒子分散性降低、以及因凝聚導致生成粗大物,容易造成纖維表面凹凸呈不均勻,因而無機粒子的添加方法較佳為能維持良好分散性的方法。In particular, the polyamide with an aliphatic hydrocarbon chain of C7 or above used in the present invention is compared to the polyamide 6 and polyamide 66 (polyamide with a C6 aliphatic hydrocarbon chain) commonly used in clothing materials. amine), the dispersion of inorganic particles is poor. The reason is that polyamides with aliphatic carbon hydrocarbon chains of C7 or above reduce the density of amide bonds, making the polymer less polar. This increases the interfacial tension difference between the inorganic particles and the highly polar inorganic particles, causing the inorganic particles to collapse. Caused by deterioration of cohesion. Accordingly, since the dispersibility of the inorganic particles in the polyamide polymer decreases and the aggregation leads to the formation of coarse particles, which can easily lead to uneven unevenness on the fiber surface, the method for adding the inorganic particles is preferably a method that maintains good dispersion. .

[聚醯胺複絲之製造方法] 列舉製造本發明之聚醯胺複絲之一例。 [Manufacturing method of polyamide multifilament yarn] An example of manufacturing the polyamide multifilament yarn of the present invention is given.

<添加無機粒子> 將無機粒子添加於聚醯胺中的方法,係有在製造碎片的聚合時便添加之情況,以及施行熔融混練的情況。為提升無機粒子分散性的無機粒子添加方法,較佳係例如適當活用以下方法。 <Add inorganic particles> Methods for adding inorganic particles to polyamide include adding them during polymerization to produce chips, or performing melt-kneading. In order to improve the dispersibility of the inorganic particles, the method for adding inorganic particles is preferably appropriately utilized, for example.

(聚合時添加) 在聚合時添加的方法,係在製備聚合物原料調製液時,對前述聚醯胺原料單體的水溶液,添加無機粒子、分散劑、適量末端基調節劑、耐候劑、抗氧化劑,經由攪拌、循環而施行混合・溶解・分散。為使分散性良好,較佳為預先將分散劑與酸末端基調節劑混合後,才添加無機粒子的方法。藉此,藉由分散劑、與被覆著無機粒子表面的成分間之相互作用,便可抑制無機粒子之凝聚及聚合物中粗大粒子之生成。 (added during aggregation) The method of adding during polymerization is to add inorganic particles, dispersant, an appropriate amount of terminal group regulator, weathering agent, and antioxidant to the aqueous solution of the polyamide raw material monomer when preparing the polymer raw material preparation liquid, and stir, Mixing, dissolving, and dispersing are performed in a cycle. In order to achieve good dispersion, it is preferable to add the inorganic particles after mixing the dispersant and the acid terminal group regulator in advance. Thereby, through the interaction between the dispersant and the components covering the surface of the inorganic particles, the aggregation of the inorganic particles and the generation of coarse particles in the polymer can be suppressed.

・分散劑 當無機粒子係硫酸鋇、氧化鈦、氧化鎂、氧化鋁的情況,分散劑較佳係使用聚丙烯酸。配合該等無機粒子的含有率再行適當調整分散劑的含有率,當聚丙烯酸含有率相對於無機粒子為0.01~0.15%的情況,可獲得良好分散性,屬更佳。 ・Dispersant When the inorganic particles are barium sulfate, titanium oxide, magnesium oxide, or aluminum oxide, the dispersant is preferably polyacrylic acid. The content of the dispersant is appropriately adjusted according to the content of the inorganic particles. When the content of polyacrylic acid is 0.01~0.15% relative to the inorganic particles, good dispersion can be obtained, which is better.

(熔融混練) 於熔融混練的情況,較佳係利用擠壓機等,將本發明所使用具C7以上之脂肪族烴鏈的聚醯胺碎片與無機粒子依熔融狀態施行混練的方法。又,即便為此情況,亦可使用與上述同樣的分散劑。 (melt kneading) In the case of melt-kneading, it is preferable to use an extruder or the like to knead the polyamide fragments and inorganic particles having a C7 or higher aliphatic hydrocarbon chain used in the present invention in a molten state. In addition, even in this case, the same dispersant as described above can be used.

・熔融黏度 當利用熔融混練進行添加的情況,較佳為將聚醯胺熔融溫度的熔融黏度設為3500poise以下。藉由將熔融黏度設在3500poise以下,即使強化添加無機粒子後之混練,仍可使無機粒子的分散呈良好,可抑制無機粒子之凝聚及聚合物中粗大粒子之生成。另外,1poise=0.1Pa・s。 ・Melt viscosity When adding by melt kneading, it is preferable to set the melt viscosity of the polyamide melting temperature to 3500 poise or less. By setting the melt viscosity below 3500 poise, even if the kneading after adding inorganic particles is intensified, the inorganic particles can still be well dispersed, and the aggregation of the inorganic particles and the generation of coarse particles in the polymer can be suppressed. In addition, 1poise=0.1Pa·s.

若例示熔融混練方法,係可使用例如:在碎片中摻合無機粒子並施行熔融的方法,將含有高濃度無機粒子的母料碎片與碎片進行摻合並熔融的方法,在熔融狀態聚合物中添加無機粒子並施行熔融混練的方法等中之任一方法。 於母料碎片摻合法的情況,為防止因無機粒子凝聚導致濃度均勻性降低,較佳為將母料碎片的粒子濃度設在20質量%以下。 If the melt-kneading method is exemplified, for example, a method of blending and melting inorganic particles into chips, a method of blending and melting masterbatch chips containing high-concentration inorganic particles with chips, and adding inorganic particles to a molten polymer can be used. Inorganic particles are melted and kneaded using any method. In the case of the masterbatch chip blending method, in order to prevent a decrease in concentration uniformity due to aggregation of inorganic particles, it is preferable to set the particle concentration of the masterbatch chips to 20 mass % or less.

・熔融過濾 經熔融混練後,較佳為使凝聚的無機粒子分散。此處,在熔融擠出時,較佳為通過過濾用過濾器實施過濾。過濾用過濾器較佳係SAS製不織布且孔徑未滿50微米的過濾器。 ・Melt filtration After melting and kneading, it is preferable to disperse the agglomerated inorganic particles. Here, during melt extrusion, filtration is preferably performed through a filtration filter. The filter used for filtration is preferably a filter made of SAS nonwoven fabric with a pore size of less than 50 microns.

<製絲> 針對無機粒子添加,於聚合時添加係依照習知方法將聚合物熔融,且當熔融混練的情況,採用上述熔融黏度、混練方法、熔融過濾,將已熔融的聚醯胺聚合物施行過濾後,利用齒輪泵施行輕量化、輸送,再從紡絲吐絲口吐出,使其通過朝設置在紡絲吐絲口正下方之紡絲吐絲口面噴射蒸氣的蒸氣噴出裝置,以及在蒸氣噴射裝置下游端所設置且從冷卻裝置吹出冷卻風氣流的區域,而使絲線冷卻固化至室溫,接著利用供油裝置進行供油而將絲線集束,利用流體交絡噴嘴裝置進行交絡,然後通過牽引滾筒、延伸滾筒。此時,將絲線依照牽引滾筒與延伸滾筒的圓周速度比施行延伸。又,將絲線利用延伸滾筒施行加熱而熱定型,再利用捲線機(捲取裝置)進行捲取。 <Silk making> For the addition of inorganic particles, the polymer is melted according to conventional methods during polymerization, and in the case of melting and kneading, the above-mentioned melt viscosity, kneading method, and melt filtration are used to filter the melted polyamide polymer. The gear pump is used to reduce the weight and transport, and then it is discharged from the spinning outlet, passing through a steam ejection device that injects steam toward the surface of the spinning outlet located directly below the spinning outlet, and the steam injection device An area is provided at the downstream end and the cooling air flow is blown out from the cooling device to cool and solidify the threads to room temperature. Then, the oil supply device is used to supply oil to bundle the threads, and the fluid interlacing nozzle device is used to intertwine, and then passes through the traction roller, Extension roller. At this time, the wire is stretched according to the circumferential speed ratio of the traction drum and the stretching drum. Furthermore, the yarn is heated and heat-set using a drawing roller, and is then wound up using a winding machine (winding device).

於延伸絲的情況,較佳為依高牽伸比・低倍率延伸進行製絲,可抑制毛球鬆垮產生。牽伸比較佳係設為100~300、延伸倍率較佳係設為1.1~2.0倍。藉由設為高牽伸比,纖維構造直到延伸前均呈安定,藉由延伸時的延伸點呈安定,便有助於抑制毛球鬆垮產生。所謂「牽伸比」係指牽引滾筒圓周速度除以吐絲口之吐出線速度的數值,依以下算式計算出。 牽伸比=(牽引滾筒圓周速度)/(吐出線速度) In the case of drawing yarn, it is better to make yarn with a high draft ratio and low stretching ratio, which can prevent the occurrence of loose hair balls. The draft is preferably set to 100~300, and the stretch ratio is preferably set to 1.1~2.0 times. By setting a high draft ratio, the fiber structure is stable until stretching. By stabilizing the extension point during stretching, it helps to suppress the occurrence of loose hair balls. The so-called "draft ratio" refers to the value of the peripheral speed of the traction drum divided by the linear speed of the spinning nozzle, and is calculated according to the following formula. Draft ratio = (circular speed of traction drum)/(discharge linear speed)

本發明的聚醯胺複絲不僅侷限於上述製造方法,亦可利用牽引滾筒與延伸滾筒間未施行延伸的高配向未延伸絲,又,亦可利用在獲得未延伸絲之後才施行延伸的二階段步驟進行製造。The polyamide multifilament of the present invention is not limited to the above-mentioned manufacturing method. Highly oriented unstretched yarns that are not stretched between the drawing drum and the drawing drum can also be used. Furthermore, the polyamide multifilament yarns that are stretched after obtaining the unstretched yarns can also be used. Manufacturing is carried out step by step.

當本發明的聚醯胺複絲形成高配向未延伸絲時,可利用一般採用地方法施行絲加工。絲加工係可適當選擇例如:摩擦假撚加工、錠子假撚加工、複合假撚加工等。When the polyamide multifilament of the present invention is formed into a highly oriented unstretched yarn, the yarn processing can be carried out by a commonly used method. The yarn processing system can be appropriately selected, such as friction false twisting, spindle false twisting, composite false twisting, etc.

[織物] 本發明亦關於其中一部分含有上述聚醯胺複絲的織物。 本發明的聚醯胺複絲係利用一般使用的方法進行製織便可形成織物。織物的製織係可從例如:平織、梭織、緞紋織、以及紗或絽等羅紋組織、多臂組織(dobby weave)、提花組織(jacquard weave)等一般織物組織中適當選擇。 [Fabric] The present invention also relates to a fabric partially containing the above-mentioned polyamide multifilament yarn. The polyamide multifilament yarn of the present invention can be woven into a fabric by using commonly used methods. The weaving system of the fabric can be appropriately selected from general fabric weaves such as plain weave, woven weave, satin weave, rib weave such as yarn or quilted weave, dobby weave, jacquard weave, etc.

本發明的聚醯胺複絲係可直接使用於織編物。亦可更進一步形成布帛後再施行染色、或接著再施行後加工,相關最終定型條件亦可依照公知方法實施,染料係可使用酸性染料、反應染料,當然顏色等亦無限定。The polyamide multifilament system of the present invention can be directly used in woven fabrics. The fabric can also be further formed and then dyed or post-processed. The relevant final setting conditions can also be implemented according to known methods. The dye system can use acid dyes and reactive dyes. Of course, the color is not limited.

本發明之聚醯胺複絲較佳係使用於戶外夾克、羽絨外套,但藉由適當選擇布帛組織,亦可使用於襯衫、內褲等。 [實施例] The polyamide multifilament of the present invention is preferably used in outdoor jackets and down jackets, but by appropriately selecting the fabric structure, it can also be used in shirts, underwear, etc. [Example]

以下,利用實施例針對本發明進行更詳細說明。Hereinafter, the present invention will be described in more detail using examples.

A.強度、伸度 根據JIS L1013(2010)拉伸強度及延伸率測定纖維試料。試驗條件係依試驗機種類為定速緊張型、抓持間隔50cm、拉伸速度50cm/分實施。另外,當切斷時的強度小於最高強度的情況,便測定最高強度與此時的延伸率。 強度與伸度係依下式求取。 強度=切斷時的強度(cN)/纖度(dtex) 伸度=切斷時的延伸率(%) A.Strength and elongation The fiber sample was measured according to JIS L1013 (2010) tensile strength and elongation. The test conditions are based on the type of testing machine: constant speed tension type, gripping interval of 50cm, and stretching speed of 50cm/min. In addition, when the strength at the time of cutting is less than the maximum strength, the maximum strength and the elongation at that time are measured. Strength and elongation are determined according to the following formula. Strength = strength when cut (cN)/denier (dtex) Elongation = elongation when cutting (%)

B.纖度 在1.125m/圈的搖紗機上安裝纖維試料,進行500旋轉而製作環狀絞紗,利用熱風乾燥機施行乾燥後(105±2℃、60分),使用天秤秤量絞紗質量,從和標準回潮率相乘後的值計算出纖度(dtex)。 B. Fineness Install the fiber sample on a 1.125m/turn loom and perform 500 rotations to make a ring-shaped skein. After drying with a hot air dryer (105±2°C, 60 minutes), use a scale to weigh the skein quality. The fineness (dtex) is calculated by multiplying the standard moisture regain.

C.硫酸相對黏度 將聚醯胺碎片試料或纖維試料0.25g相對於濃度98質量%硫酸100ml溶解成1g,使用奧士華式黏度計測定25℃之流下時間(T1)。接著,測定僅有濃度98質量%硫酸的流下時間(T2)。將T1相對於T2的比(即T1/T2)設為硫酸相對黏度。 C. Relative viscosity of sulfuric acid Dissolve 0.25g of the polyamide fragment sample or the fiber sample into 100 ml of sulfuric acid with a concentration of 98% by mass, and measure the flowing time (T1) at 25°C using an Oswald viscometer. Next, the flowing time (T2) of only sulfuric acid with a concentration of 98% by mass was measured. Let the ratio of T1 to T2 (ie, T1/T2) be the relative viscosity of sulfuric acid.

D.無機粒子含量(灰分量) 根據JIS L1013(2010)灰分測定纖維試料。 將坩堝在設定800℃之電爐中空燒2小時,經1小時冷卻後施行精秤(A1)。在該坩堝中秤量(S)經乾燥至水分量未滿300ppm的纖維試料,利用電爐與氣體燃燒器施行加熱延燒。接著,將該坩堝在800℃電爐中加熱2小時,經1小時冷卻後施行精秤。重複利用電爐與氣體燃燒器施行加熱延燒、利用電爐施行加熱、以及冷卻後的精秤,重複直到成為與前一次精秤結果相同之值為止。將依此獲得的精秤結果設為(A2),依下式求取無機粒子含量。 無機粒子含量(質量%)=(A2-A1)/S×100。 D. Inorganic particle content (ash content) The fiber sample was measured according to JIS L1013 (2010) ash content. The crucible was hollow-fired in an electric furnace set at 800°C for 2 hours, and then cooled for 1 hour before precision weighing (A1) was performed. The fiber sample (S) dried to a moisture content of less than 300 ppm was weighed in the crucible, and heated and burned using an electric furnace and a gas burner. Next, the crucible was heated in an 800°C electric furnace for 2 hours, cooled for 1 hour, and then accurately weighed. Repeat using the electric furnace and gas burner to heat and burn, use the electric furnace to heat, and cool the precision scale until it reaches the same value as the previous precision scale result. Let the precision weighing result obtained in this way be (A2), and calculate the inorganic particle content according to the following formula. Inorganic particle content (mass %) = (A2-A1)/S×100.

E.生物基碳濃度 將纖維試料根據ASTM D6866法(20-B),利用放射性碳分析進行生物基碳濃度(%)分析。 E. Biobased carbon concentration The fiber sample was analyzed for biobased carbon concentration (%) using radioactive carbon analysis according to ASTM D6866 method (20-B).

F.儲存彈性模數 將纖維試料使用AND公司製動態黏彈性自動測定器 DDV-GP(Rheovibron),針對從35℃至100℃之溫度掃描時的動態黏彈性施行評價。考量通過與導絲器等機械接觸部位時的絲溫度,針對50℃與80℃等2水準的黏彈性行為施行分析。因為在該溫度範圍內由彈性行為主導,因而表示儲存彈性模數。 F.Storage elastic modulus The fiber sample was evaluated for dynamic viscoelasticity during temperature scanning from 35°C to 100°C using an automatic dynamic viscoelasticity measuring instrument DDV-GP (Rheovibron) manufactured by AND Corporation. The viscoelastic behavior at two levels, such as 50°C and 80°C, was analyzed by considering the temperature of the yarn when it passes through mechanical contact parts such as the yarn guide. Since elastic behavior dominates in this temperature range, it represents the storage elastic modulus.

G.絲-金屬間之動摩擦係數 使用圖2所示由:張力缺口環導絲器8、張力計測部9,10、張力滾筒11、驅動單元12、數據處理部、及記錄器構成的英光產業(股)製運行絲摩擦係數測定裝置,依如圖2所示設定測定絲的運行絲道。張力滾筒11係使用表面經鍍金屬鉻而鏡面化,直徑15mm、長度100mm的固定金屬圓筒,使測定絲90°接觸於該張力滾筒11(金屬摩擦體d),將絲的運行速度設為2.5m/分,且將接觸於張力滾筒11(金屬摩擦體d)前的絲線張力(T1)設定為10cN,運行60秒鐘。連續測定此時的接觸於張力滾筒11(金屬摩擦體d)前的絲線張力(T1、張力計測部9)、與接觸後的絲線張力(T2、張力計測部10),並記錄於記錄器中。將記錄器中所記錄的各平均值設為(T1)與(T2),使用下式計算出絲-金屬間的動摩擦係數(μd)。 動摩擦係數(μd)=1/(0.5×π)×log(T2/T1) G. Kinetic friction coefficient between wire and metal The friction coefficient of the running yarn manufactured by Yingko Industrial Co., Ltd. is measured using the tension notch ring yarn guide 8, tension measurement parts 9, 10, tension roller 11, drive unit 12, data processing part, and recorder shown in Figure 2. Device, set the running wire path of the measuring wire as shown in Figure 2. The tension roller 11 is a fixed metal cylinder with a surface of 15 mm in diameter and 100 mm in length that is mirror-like plated with metallic chromium. The measuring wire is contacted with the tension roller 11 (metal friction body d) at 90°, and the running speed of the wire is set to 2.5m/min, and set the thread tension (T1) before contacting the tension roller 11 (metal friction body d) to 10cN, and run for 60 seconds. At this time, the yarn tension before contacting the tension roller 11 (metal friction body d) (T1, tension measurement part 9) and the yarn tension after contact (T2, tension measurement part 10) are continuously measured, and recorded in the recorder. . Let the average values recorded in the recorder be (T1) and (T2), and calculate the dynamic friction coefficient (μd) between the wire and the metal using the following equation. Dynamic friction coefficient (μd)=1/(0.5×π)×log(T2/T1)

H.毛球鬆垮個數 將纖維試料依600m/分的速度反繞40分鐘,在距反繞中之運行絲15mm的地方設置東麗工程公司(Toray Engineering)製MFC-200雷射式毛球檢測機,將所檢測到的缺陷個數換算為每10000m的個數。 H. Number of loose hair balls The fiber sample was rewinded at a speed of 600m/min for 40 minutes. An MFC-200 laser ball detector manufactured by Toray Engineering was installed 15mm away from the running yarn during rewinding. The number of defects is converted into the number per 10000m.

I.織物製品之評價 (a)通氣度 針對實施例・比較例所獲得織物評價通氣度。通氣度係根據JIS L1096(2010),依通氣性弗雷澤法(A法)進行測定。針對相同織物測定3次,從平均值依下述基準施行4階段評價。 A:未滿0.7cc B:0.7cc以上且未滿1.0cc、 C:1.0cc以上且未滿1.3cc、 D:1.3cc以上 將A、B設為合格。 I. Evaluation of fabric products (a) Ventilation The fabrics obtained in Examples and Comparative Examples were evaluated for air permeability. The air permeability is measured according to JIS L1096 (2010) and the air permeability Fraser method (A method). The same fabric was measured three times, and a four-stage evaluation was performed based on the average value according to the following standards. A: Less than 0.7cc B: 0.7cc or more and less than 1.0cc, C: 1.0cc or more and less than 1.3cc, D: 1.3cc or more Set A and B as qualified.

(b)製品品質 目視檢査織物每50m的斑點與條痕產生狀態,並依照下述基準施行評價。 A:沒有條痕與斑點、具優異品質。 B:雖有些微條痕與斑點產生,但在使用為製品時並不會有問題。 C:產生條痕或斑點,無法使用為製品。 將A、B設為合格。 (b) Product quality The fabric is visually inspected for spots and streaks every 50 meters, and evaluated based on the following standards. A: No streaks or spots, excellent quality. B: Although some micro streaks and spots are produced, there will be no problems when using it as finished products. C: Streaks or spots are produced and the product cannot be used. Set A and B as qualified.

(c)高階步驟順暢性(表中簡記為「高階順暢性」) 利用噴水式無梭織機,依織機轉數750rpm、緯紗長1620mm的方式製織10匹(1000m/匹)平織物,針對此時因斷絲造成的停機次數,依照下述基準施行評價。 A:未滿2次 B:2次以上且未滿4次 C:4次以上且未滿6次 D:6次以上 將A、B設為合格。 (c) High-order step smoothness (abbreviated as “high-order smoothness” in the table) A water-jet shuttleless loom was used to weave 10 pieces of flat fabric (1000m/piece) using a loom speed of 750rpm and a weft length of 1620mm. The number of downtimes caused by broken filaments at this time was evaluated according to the following criteria. A: Less than 2 times B: More than 2 times and less than 4 times C: More than 4 times but less than 6 times D: More than 6 times Set A and B as qualified.

[實施例1] (聚醯胺複絲之製造) 使用醯胺鍵間具碳數C8之脂肪族烴鏈的聚醯胺610(硫酸相對黏度2.7、熔點:225℃、280℃下之熔融黏度為700poise、比重1.07g/cm 3、熔融密度0.92g/cm 3),製造含氧化鈦20質量%之聚醯胺610的母料碎片。依絲中的氧化鈦含量成為0.3質量%之方式,獲得經添加該母料碎片1.5質量%的聚醯胺610碎片。將該碎片的水分率調整為0.14質量%,投入圖1所示紡絲機中,依紡絲溫度280℃熔融,利用SAS製不織布且孔徑10微米的過濾器施行過濾,再從具96孔吐出孔徑為0.20mm、孔長為0.70mm之圓孔的紡絲吐絲口1,依吐出量39.6g/min(吐出線速度19.8m/min)紡出。紡出絲線利用冷卻裝置2噴吹冷風而冷卻固化,經供油裝置3供油後,以流體交絡噴嘴裝置4賦予交絡,再利用牽引滾筒5依圓周速度(牽引速度)3460m/分(設定值、牽伸比175.1)施行牽引。接著,將經牽引滾筒5牽引過的絲線,利用表面溫度170℃的延伸滾筒6進行牽引,再於滾筒間(滾筒5與滾筒6間)延伸為延伸倍率1.30倍,利用捲線機7依捲取速度4500m/分(設定值)捲取,獲得4條22dtex-24支絲的聚醯胺610複絲。針對所獲得之聚醯胺複絲評價纖度、強伸度、每10000m的毛球鬆垮個數。結果如表1所示。另外,纖維長邊方向的灰分量變動CV值係0.1。 [Example 1] (Production of polyamide multifilament) Polyamide 610 having a C8 aliphatic hydrocarbon chain between amide bonds was used (sulfuric acid relative viscosity: 2.7, melting point: 225°C, melt viscosity at 280°C Masterbatch chips of polyamide 610 containing 20% by mass of titanium oxide were produced with a specific gravity of 700poise, a specific gravity of 1.07g/cm 3 and a melt density of 0.92g/cm 3 ). The titanium oxide content in the silk was adjusted to 0.3% by mass to obtain polyamide 610 chips to which 1.5% by mass of the masterbatch chips were added. The moisture content of the fragments was adjusted to 0.14% by mass, put into the spinning machine shown in Figure 1, melted at a spinning temperature of 280°C, filtered using a nonwoven filter made of SAS with a pore size of 10 microns, and then discharged from the 96-hole tool. The spinning and spinning nozzle 1 with a round hole with a hole diameter of 0.20mm and a hole length of 0.70mm can be spun with an output of 39.6g/min (discharge linear speed of 19.8m/min). The spun yarn is cooled and solidified by blowing cold air from the cooling device 2. After oil is supplied by the oil supply device 3, it is interlaced with the fluid interlacing nozzle device 4, and then the traction drum 5 is used to follow the circumferential speed (traction speed) of 3460m/min (set value , draft ratio 175.1) to perform traction. Then, the thread drawn by the drawing roller 5 is drawn by the stretching roller 6 with a surface temperature of 170°C, and then stretched between the rollers (between the roller 5 and the roller 6) to an extension magnification of 1.30 times, and is wound up by the winding machine 7 Winding at a speed of 4500m/min (set value), four polyamide 610 multifilaments of 22dtex-24 filaments were obtained. The obtained polyamide multifilament yarn was evaluated for its fineness, strength and elongation, and the number of loose balls per 10,000 meters. The results are shown in Table 1. In addition, the CV value of ash content variation in the fiber longitudinal direction is 0.1.

(織物之製造) 對所獲得複絲1000條施行整經並捲成束,再對已捲繞成束的絲施行上糊,經乾燥再施行經絲準備。接著,通過噴水織機的筘,將所獲得之複絲植入緯紗中而製織平織物。所製織的織物施行精練、170℃熱定型(中間定型)、染色、170℃軋光加工,而獲得戶外夾克用織物。針對所獲得之織物施行評價,結果如表1所示。 (Manufacturing of fabrics) The 1,000 obtained multifilament yarns were warped and rolled into bundles, and then the yarns that had been wound into bundles were pasted, dried, and then prepared for warp yarn preparation. Then, the obtained multifilament is embedded into the weft yarn through the reed of a water-jet loom to produce a plain fabric. The woven fabric is scouring, heat-set at 170°C (intermediate setting), dyed, and calendered at 170°C to obtain fabric for outdoor jackets. The obtained fabric was evaluated, and the results are shown in Table 1.

織物製造的步驟順暢性極良好。通氣度特性亦優異,製品品質亦優異。The fabric manufacturing steps are extremely smooth. The air permeability characteristics are also excellent, and the product quality is also excellent.

[表1] 表1                                  實施例1 實施例2 實施例3 比較例1 實施例4 實施例5 比較例2 實施例6 實施例7 比較例3 聚合物 聚合物種類 N610 N610 N610 N610 N610 N610 N610 N610 N610 N610 硫酸相對黏度 2.7 2.7 2.7 2.7 2.7 2.7 2.7 2.7 2.7 2.7 生物基碳濃度(%) 63 63 63 63 63 63 63 63 63 63 原絲 無機粒子種類 氧化鈦 硫酸鋇 氧化鎂 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 無機粒子含量(質量%) 0.3 0.5 0.04 0 0.01 5 6 0.3 0.3 0.3 纖度(dtex) 22 22 22 22 22 22 22 35 22 22 絲數 24 24 24 24 24 24 24 72 20 7 單絲纖度(dtex) 0.92 0.92 0.92 0.92 0.92 0.92 0.92 0.49 1.10 3.14 強度(cN/dtex) 5.0 5.0 5.0 4.8 4.9 4.5 4.1 3.7 3.5 5.3 伸度(%) 48 48 48 47 48 47 47 65 80 48 儲存彈性模數50°C(GPa) 3.2 3.2 3.2 3.5 3.4 2.9 2.5 3.1 3.0 3.3 儲存彈性模數80°C(GPa) 2.4 2.4 2.4 2.5 2.4 2.0 1.8 2.3 2.2 2.5 動摩擦係數(μd) 0.4 0.4 0.4 1.2 0.6 0.3 0.3 0.6 0.5 1.1 毛球鬆垮(個/1萬m) 0 0 0.4 2.9 0.8 0.8 2.1 0.8 0.4 0 織物評價 通氣度 A A A B A A B A B D 製品品質 A A A C A B C B A A 高階順暢性 A A A C B B D B A A       N610 :聚醯胺610 [Table 1] Table 1 Example 1 Example 2 Example 3 Comparative example 1 Example 4 Example 5 Comparative example 2 Example 6 Example 7 Comparative example 3 polymer Polymer type N610 N610 N610 N610 N610 N610 N610 N610 N610 N610 Relative viscosity of sulfuric acid 2.7 2.7 2.7 2.7 2.7 2.7 2.7 2.7 2.7 2.7 Biobased carbon concentration (%) 63 63 63 63 63 63 63 63 63 63 raw silk Types of inorganic particles titanium oxide barium sulfate magnesium oxide titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide Inorganic particle content (mass %) 0.3 0.5 0.04 0 0.01 5 6 0.3 0.3 0.3 Fineness (dtex) twenty two twenty two twenty two twenty two twenty two twenty two twenty two 35 twenty two twenty two Number of threads twenty four twenty four twenty four twenty four twenty four twenty four twenty four 72 20 7 Single filament fineness (dtex) 0.92 0.92 0.92 0.92 0.92 0.92 0.92 0.49 1.10 3.14 Strength(cN/dtex) 5.0 5.0 5.0 4.8 4.9 4.5 4.1 3.7 3.5 5.3 Elongation(%) 48 48 48 47 48 47 47 65 80 48 Storage elastic modulus 50°C (GPa) 3.2 3.2 3.2 3.5 3.4 2.9 2.5 3.1 3.0 3.3 Storage elastic modulus 80°C (GPa) 2.4 2.4 2.4 2.5 2.4 2.0 1.8 2.3 2.2 2.5 Dynamic friction coefficient (μd) 0.4 0.4 0.4 1.2 0.6 0.3 0.3 0.6 0.5 1.1 Loose hair balls (pieces/10,000 m) 0 0 0.4 2.9 0.8 0.8 2.1 0.8 0.4 0 fabric evaluation Ventilation A A A B A A B A B D Product quality A A A C A B C B A A High level smoothness A A A C B B D B A A N610: Polyamide 610

[實施例2] 除將所添加的無機粒子變更為硫酸鋇,且將絲中含量變更為0.5質量%之外,其餘均依照與實施例1同樣的方法,獲得22dtex-24支絲的聚醯胺610複絲,依照與實施例1同樣的方法製作織物。評價結果如表1所示。 [Example 2] Except that the added inorganic particles were changed to barium sulfate and the content in the silk was changed to 0.5% by mass, the same method as in Example 1 was followed to obtain a polyamide 610 multifilament of 22dtex-24 yarns. Fabric was produced according to the same method as Example 1. The evaluation results are shown in Table 1.

[實施例3] 除將所添加的無機粒子變更為氧化鎂,且將絲中含量變更為0.04質量%之外,其餘均依照與實施例1同樣的方法,獲得22dtex-24支絲的聚醯胺610複絲,依照與實施例1同樣的方法製作織物。評價結果如表1所示。 [Example 3] Except that the added inorganic particles were changed to magnesium oxide and the content in the silk was changed to 0.04% by mass, the same method as in Example 1 was followed to obtain a polyamide 610 multifilament of 22dtex-24 filaments. Fabric was produced according to the same method as Example 1. The evaluation results are shown in Table 1.

[實施例4、5、比較例1、2] 除將氧化鈦含量變更如表1所記載之外,其餘均依照與實施例1同樣的方法,獲得22dtex-24支絲的聚醯胺610複絲,依照與實施例1同樣的方法製作織物。評價結果如表1所示。 [Examples 4 and 5, Comparative Examples 1 and 2] Except for changing the titanium oxide content as described in Table 1, the same method as in Example 1 was followed to obtain polyamide 610 multifilament of 22dtex-24 filaments, and the fabric was produced in the same method as in Example 1. The evaluation results are shown in Table 1.

[實施例6] 除使用具有144孔吐出孔徑為0.20mm、孔長為0.70mm之圓孔的紡絲吐絲口,且未施行延伸(延伸倍率1.0倍),並將捲取速度變更為3500m/分之外,其餘均依照與實施例1同樣的方法,獲得44dtex-72支絲由聚醯胺610複絲形成的高配向未延伸絲。 [Example 6] In addition to using a spinning nozzle with 144 round holes with a discharge hole diameter of 0.20mm and a hole length of 0.70mm, no stretching (stretch ratio 1.0 times) was performed, and the winding speed was changed to 3500m/min. In the rest, the same method as in Example 1 was followed to obtain 44dtex-72 highly oriented unstretched yarns formed from polyamide 610 multifilament yarns.

(絲加工) 所獲得高配向未延伸絲利用三軸摩擦型摩擦圓盤式延伸摩擦假撚裝置,施行延伸摩擦假撚加工。從圓周速率550m/分的供應滾筒,供應給經加熱至170℃的接觸型假撚加熱器,依延伸1.5倍、盤轉數7500rpm、圓盤徑φ51、D/Y比2.18、假撚係數30000施行延伸同步假撚加工,獲得35dtex-72支絲由聚醯胺610形成的假撚加工絲(D:供應滾筒速度(m/分)、Y:盤旋轉速度(m/分))。使用所獲得之假撚加工絲,依照與實施例1同樣的方法製作織物。結果如表1所示。 (Wire processing) The obtained high-alignment unstretched yarn is subjected to stretch friction and false twisting processing using a triaxial friction-type friction disc-type stretch friction and false twisting device. From a supply drum with a peripheral speed of 550m/min, it is supplied to a contact type false twist heater heated to 170°C, with an extension of 1.5 times, a disc rotation speed of 7500rpm, a disc diameter of φ51, a D/Y ratio of 2.18, and a false twist coefficient of 30000 Perform stretching and synchronous false twist processing to obtain 35dtex-72 false twisted yarn made of polyamide 610 (D: supply drum speed (m/min), Y: disc rotation speed (m/min)). Using the obtained false-twisted yarn, a fabric was produced in the same manner as in Example 1. The results are shown in Table 1.

[實施例7] 除使用具有60孔吐出孔徑為0.20mm、孔長為0.70mm之圓孔的紡絲吐絲口,且未施行延伸(延伸倍率1.0倍),並將捲取速度變更為4000m/分之外,其餘均依照與實施例1同樣的方法,獲得26dtex-20支絲由聚醯胺610複絲形成的高配向未延伸絲。依照與實施例6同樣的方法施行絲加工,獲得22dtex-20支絲的聚醯胺610之假撚加工絲。使用所獲得假撚加工絲,依照與實施例1同樣的方法製作織物。結果如表1所示。 [Example 7] In addition to using a spinning nozzle with 60 round holes with a discharge hole diameter of 0.20mm and a hole length of 0.70mm, no stretching (stretch ratio 1.0 times) was performed, and the winding speed was changed to 4000m/min. In the rest, the same method as in Example 1 was followed to obtain a 26dtex-20 highly oriented unstretched yarn formed from polyamide 610 multifilament. The yarn was processed in the same manner as in Example 6 to obtain a false-twisted yarn of polyamide 610 with 22 dtex-20 yarn counts. Using the obtained false-twisted yarn, a fabric was produced in the same manner as in Example 1. The results are shown in Table 1.

[比較例3] 使用具有28孔吐出孔徑為0.30mm、孔長為0.75mm之圓孔的紡絲吐絲口,且將延伸倍率設為1.5倍、捲取速度變更為4500m/分之外,其餘均依照與實施例1同樣的方法,獲得22dtex-7支絲的聚醯胺610複絲,依照與實施例1同樣的方法製作織物。評價結果如表1所示。 [Comparative example 3] Use a spinning nozzle with 28 round holes with a discharge hole diameter of 0.30mm and a hole length of 0.75mm, set the elongation ratio to 1.5 times, and change the winding speed to 4500m/min. The rest are implemented in accordance with In the same method as Example 1, polyamide 610 multifilament yarn with 22dtex-7 branches was obtained, and fabrics were produced in the same method as Example 1. The evaluation results are shown in Table 1.

[實施例8] 除使用醯胺鍵間具有碳數C8之脂肪族烴鏈的聚醯胺510(硫酸相對黏度2.8、熔點:225℃、280℃下之熔融黏度為800poise、比重1.07g/cm 3、熔融密度0.92g/cm 3),且將延伸倍率變更為1.4倍之外,其餘均依照與實施例1同樣的方法,獲得22dtex-24支絲的聚醯胺510複絲,依照與實施例1同樣的方法製作織物。評價結果如表2所示。 [Example 8] In addition to using polyamide 510 with an aliphatic hydrocarbon chain of C8 between the amide bonds (relative viscosity of sulfuric acid: 2.8, melting point: 225°C, melt viscosity at 280°C is 800 poise, specific gravity: 1.07g/cm 3. The melt density is 0.92g/cm 3 ), and the stretching ratio is changed to 1.4 times. The rest are carried out in the same manner as in Example 1 to obtain polyamide 510 multifilament of 22dtex-24 filaments. According to the implementation Make the fabric in the same way as Example 1. The evaluation results are shown in Table 2.

[表2] 表2                                  實施例8 比較例4 比較例5 實施例9 比較例6 比較例7 實施例10 比較例8 比較例9 參考例11 聚合物 聚合物種類 N510 N510 N510 N410 N410 N410 N11 N11 N11 N6 硫酸相對黏度 2.8 2.8 2.8 2.8 2.8 2.8 2.0 2.0 2.0 2.7 生物基碳濃度(%) 100 100 100 73 73 73 100 100 100 0 原絲 無機粒子種類 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 氧化鈦 無機粒子含量(質量%) 0.3 0 6 0.3 0 6 0.3 0 6 0 纖度(dtex) 22 22 22 22 22 22 22 22 22 22 絲數 24 24 24 24 24 24 24 24 24 24 單絲纖度(dtex) 0.92 0.92 0.92 0.92 0.92 0.92 0.92 0.92 0.92 0.92 強度(cN/dtex) 4.9 4.4 4.3 4.7 4.5 4.4 4.7 4.6 4.5 5.0 伸度(%) 48 48 47 46 47 46 48 47 46 48 儲存彈性模數50°C(GPa) 3.3 3.6 2.9 3.6 3.8 3.2 2.9 3.2 2.3 4.0 儲存彈性模數80°C(GPa) 2.4 2.6 2.1 2.9 3.0 2.5 1.9 2.1 1.4 3.3 動摩擦係數(μd) 0.4 1.1 0.2 0.3 0.9 0.2 0.6 1.3 0.5 0.4 毛球鬆垮(個/1萬m) 0.4 2.5 1.7 0 2.1 1.7 0.4 4.2 3.3 0 織物評價 通氣度 A B B A B B A B B A 製品品質 B C C A C C A C C A 高階順暢性 A D D A D D A D D A       N510:聚醯胺516、N410:聚醯胺410、N11:聚醯胺11、N6 :聚醯胺6 [Table 2] Table 2 Example 8 Comparative example 4 Comparative example 5 Example 9 Comparative example 6 Comparative example 7 Example 10 Comparative example 8 Comparative example 9 Reference example 11 polymer Polymer type N510 N510 N510 N410 N410 N410 N11 N11 N11 N6 Relative viscosity of sulfuric acid 2.8 2.8 2.8 2.8 2.8 2.8 2.0 2.0 2.0 2.7 Biobased carbon concentration (%) 100 100 100 73 73 73 100 100 100 0 raw silk Types of inorganic particles titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide titanium oxide Inorganic particle content (mass %) 0.3 0 6 0.3 0 6 0.3 0 6 0 Fineness (dtex) twenty two twenty two twenty two twenty two twenty two twenty two twenty two twenty two twenty two twenty two Number of threads twenty four twenty four twenty four twenty four twenty four twenty four twenty four twenty four twenty four twenty four Single filament fineness (dtex) 0.92 0.92 0.92 0.92 0.92 0.92 0.92 0.92 0.92 0.92 Strength(cN/dtex) 4.9 4.4 4.3 4.7 4.5 4.4 4.7 4.6 4.5 5.0 Elongation(%) 48 48 47 46 47 46 48 47 46 48 Storage elastic modulus 50°C (GPa) 3.3 3.6 2.9 3.6 3.8 3.2 2.9 3.2 2.3 4.0 Storage elastic modulus 80°C (GPa) 2.4 2.6 2.1 2.9 3.0 2.5 1.9 2.1 1.4 3.3 Dynamic friction coefficient (μd) 0.4 1.1 0.2 0.3 0.9 0.2 0.6 1.3 0.5 0.4 Loose hair balls (pieces/10,000 m) 0.4 2.5 1.7 0 2.1 1.7 0.4 4.2 3.3 0 fabric evaluation Ventilation A B B A B B A B B A Product quality B C C A C C A C C A High level smoothness A D D A D D A D D A N510: Polyamide 516, N410: Polyamide 410, N11: Polyamide 11, N6: Polyamide 6

[比較例4、5] 除將氧化鈦含量變更如表2所記載之外,其餘均依照與實施例8同樣的方法,獲得22dtex-24支絲的聚醯胺510複絲,依照與實施例1同樣的方法製作織物。評價結果如表2所示。 [Comparative Examples 4 and 5] Except for changing the titanium oxide content as described in Table 2, the same method as in Example 8 was followed to obtain polyamide 510 multifilament of 22dtex-24 filaments, and the fabric was produced in the same method as in Example 1. The evaluation results are shown in Table 2.

[實施例9] 除使用醯胺鍵間具有碳數C8之脂肪族烴鏈的聚醯胺410(硫酸相對黏度2.8、熔點:250℃、280℃下之熔融黏度為1100poise、比重1.09g/cm 3、熔融密度0.94g/cm 3),且將延伸倍率變更為1.3倍之外,其餘均依照與實施例1同樣的方法,獲得22dtex-24支絲的聚醯胺410複絲,依照與實施例1同樣的方法製作織物。評價結果如表2所示。 [Example 9] In addition to using polyamide 410 with an aliphatic hydrocarbon chain of C8 between the amide bonds (relative viscosity of sulfuric acid: 2.8, melting point: 250°C, melt viscosity at 280°C is 1100 poise, specific gravity: 1.09g/cm 3. The melt density is 0.94g/cm 3 ), and the stretching ratio is changed to 1.3 times. The rest are carried out in the same manner as in Example 1 to obtain polyamide 410 multifilament of 22dtex-24 filaments. According to the implementation Make the fabric in the same way as Example 1. The evaluation results are shown in Table 2.

[比較例6、7] 除將氧化鈦含量變更如表2所記載之外,其餘均依照與實施例9同樣的方法,獲得22dtex-24支絲的聚醯胺410複絲,依照與實施例1同樣的方法製作織物。評價結果如表2所示。 [Comparative Examples 6 and 7] Except that the titanium oxide content was changed as described in Table 2, the same method as in Example 9 was followed to obtain polyamide 410 multifilament of 22dtex-24 filaments, and the fabric was produced in the same method as in Example 1. The evaluation results are shown in Table 2.

[實施例10] 除使用醯胺鍵間具有碳數C10之脂肪族烴鏈的聚醯胺11(硫酸相對黏度2.0、熔點:187℃、235℃下之熔融黏度為1000poise、比重1.03g/cm 3、熔融密度0.89g/cm 3),且將熔融溫度變更為235℃、延伸倍率變更為1.5倍之外,其餘均依照與實施例1同樣的方法,獲得22dtex-24支絲的聚醯胺11複絲,依照與實施例1同樣的方法製作織物。評價結果如表2所示。 [Example 10] In addition to using polyamide 11 having an aliphatic hydrocarbon chain with a carbon number of C10 between the amide bonds (sulfuric acid relative viscosity: 2.0, melting point: 187°C, melt viscosity at 235°C is 1000 poise, specific gravity 1.03g/cm 3. The melt density is 0.89g/cm 3 ), except that the melting temperature is changed to 235°C and the elongation ratio is changed to 1.5 times. The rest are carried out in the same manner as in Example 1 to obtain a polyamide of 22dtex-24 filaments. 11 Multifilament, fabricate according to the same method as Example 1. The evaluation results are shown in Table 2.

[比較例8、9] 除將氧化鈦含量變更如表2所記載之外,其餘均依照與實施例10同樣的方法,獲得22dtex-24支絲的聚醯胺11複絲,依照與實施例1同樣的方法製作織物。評價結果如表2所示。 [Comparative Examples 8 and 9] Except that the titanium oxide content was changed as described in Table 2, the same method as in Example 10 was followed to obtain a polyamide 11 multifilament of 22dtex-24 filaments, and the fabric was produced in the same method as in Example 1. The evaluation results are shown in Table 2.

[參考例11] 除使用醯胺鍵間具有碳數C5之脂肪族烴鏈的聚醯胺6(硫酸相對黏度2.7、熔點:220℃、280℃下之熔融黏度為1100poise、比重1.14g/cm 3、熔融密度0.98g/cm 3),且未含氧化鈦,並將延伸倍率變更為1.7倍之外,其餘均依照與實施例1同樣的方法,獲得22dtex-24支絲的聚醯胺6複絲,依照與實施例1同樣的方法製作織物。評價結果如表2所示。 (產業上之可利用性) [Reference Example 11] In addition to using polyamide 6 having an aliphatic hydrocarbon chain with a carbon number of C5 between the amide bonds (relative viscosity of sulfuric acid: 2.7, melting point: 220°C, melt viscosity at 280°C is 1100 poise, specific gravity: 1.14g/cm 3. The melt density is 0.98g/cm 3 ), and does not contain titanium oxide. Except for changing the stretching ratio to 1.7 times, the rest are in accordance with the same method as in Example 1 to obtain polyamide 6 of 22dtex-24 filaments. Multifilament fabric was produced in the same manner as in Example 1. The evaluation results are shown in Table 2. (industrial availability)

利用本發明的聚醯胺複絲,可提供經抑制毛球鬆垮產生、且高階步驟順暢性優異、低通氣性與製品品質優異,適用於戶外夾克等的織物。Utilizing the polyamide multifilament of the present invention, it is possible to provide a fabric that suppresses the loosening of hair balls, has excellent smoothness in advanced steps, has low air permeability and excellent product quality, and is suitable for outdoor jackets and the like.

針對本發明詳細參照特定實施態樣進行說明,惟在不脫逸本發明精神與範圍內均可進行各種變更與修正,此係熟習此技術者可輕易思及。 本申請案係以2022年1月13日所提出申請的日本專利申請案(特願2022-003499)為基礎,參照其內容並援引於本案中。 The present invention is described in detail with reference to specific implementation aspects. However, various changes and modifications can be made without departing from the spirit and scope of the present invention, which can be easily understood by those skilled in the art. This application is based on the Japanese patent application (Special Application No. 2022-003499) filed on January 13, 2022, and the content is incorporated in this case with reference to the content.

1:紡絲吐絲口 2:冷卻裝置 3:供油裝置 4:流體交絡噴嘴裝置 5:牽引滾筒 6:延伸滾筒 7:捲取裝置(捲線機) 8:張力缺口環導絲器 9:張力計測部 10:張力計測部 11:張力滾筒 12:驅動單元 1: Spinning and spinning nozzle 2: Cooling device 3: Oil supply device 4: Fluid communication nozzle device 5: Traction roller 6:Extension roller 7: Coiling device (winding machine) 8: Tension notch ring wire guide 9: Tension measurement department 10: Tension measurement department 11: Tension roller 12: Drive unit

圖1係本發明之聚醯胺複絲之製造方法可使用的製造裝置之一實施態樣。 圖2係可測定絲之動摩擦係數的測定裝置之較佳實施態樣。 Figure 1 is an embodiment of a manufacturing device that can be used in the manufacturing method of polyamide multifilament of the present invention. Figure 2 shows a preferred embodiment of a measuring device capable of measuring the dynamic friction coefficient of a thread.

Claims (3)

一種聚醯胺複絲,係單絲纖度2.2dtex以下、每10000m的毛球鬆垮個數在1個以下、絲-金屬間的動摩擦係數在0.8μd以下,且醯胺鍵間具有碳數C7以上的脂肪族烴鏈。A polyamide multifilament with a single filament fineness of less than 2.2 dtex, a loose ball number of less than 1 per 10,000 m, a kinetic friction coefficient between silk and metal of less than 0.8 μd, and a carbon number of C7 between the amide bonds. The above aliphatic hydrocarbon chain. 如請求項1之聚醯胺複絲,其中,含有無機粒子0.01~5.0質量%。Such as the polyamide multifilament yarn of claim 1, which contains 0.01 to 5.0 mass% of inorganic particles. 一種織物,係其中一部分含有請求項1或2之聚醯胺複絲。A fabric, a part of which contains the polyamide multifilament of claim 1 or 2.
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