TW200532061A - Conjugated fiber and method for producing the same - Google Patents

Conjugated fiber and method for producing the same Download PDF

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Publication number
TW200532061A
TW200532061A TW093117461A TW93117461A TW200532061A TW 200532061 A TW200532061 A TW 200532061A TW 093117461 A TW093117461 A TW 093117461A TW 93117461 A TW93117461 A TW 93117461A TW 200532061 A TW200532061 A TW 200532061A
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Taiwan
Prior art keywords
molecular weight
spinning
fiber
temperature
composite fiber
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TW093117461A
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Chinese (zh)
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TWI286167B (en
Inventor
Sung-Jin Oh
Hyoung-Jae Lee
Yang-Kuk Son
Ik-Hyeon Kwon
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Hyosung Corp
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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
    • D01F8/00Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/04Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/14Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D10/00Physical treatment of artificial filaments or the like during manufacture, i.e. during a continuous production process before the filaments have been collected
    • D01D10/02Heat treatment
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/08Melt spinning methods
    • D01D5/098Melt spinning methods with simultaneous stretching
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/28Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
    • D01D5/30Conjugate filaments; Spinnerette packs therefor
    • D01D5/34Core-skin structure; Spinnerette packs therefor
    • 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
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/02Yarns or threads characterised by the material or by the materials from which they are made
    • D02G3/04Blended or other yarns or threads containing components made from different materials
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/22Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
    • D02G3/26Yarns or threads characterised by constructional features, e.g. blending, filament/fibre with characteristics dependent on the amount or direction of twist
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2401/00Physical properties
    • D10B2401/06Load-responsive characteristics
    • D10B2401/061Load-responsive characteristics elastic
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2401/00Physical properties
    • D10B2401/06Load-responsive characteristics
    • D10B2401/062Load-responsive characteristics stiff, shape retention

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Multicomponent Fibers (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
  • Woven Fabrics (AREA)

Abstract

To provide a crimp forming conjugate fiber excellent in stretchability and improved in product stability in post processing and a method for producing the same. The crimp forming conjugate fiber is a side-by-side or an excentric sheath-core type fiber remarkably stable for heat hysteresis, tension and the like given to the fiber in knitting, weaving and dyeing processing. The stretchable conjugate fiber produced by the invention is remarkably excellent in product stability during post processing as the fiber has high stretchability with ≥ 40% rate of crimp stretch, ≥ 70% elastic recovery factor, ≥ 155 DEG C maximum temperature of thermal contraction stress and ≥ 3% iron shrinkage of the finally processed fabric. Different fiber forming polymers having 5,000-70,000 number average molecular weight difference and 1.5-2.5 molecular weight distribution index in each fiber are used as the polymer.in the invention.

Description

200532061 五、發明說明(1) 【發明所屬之技術領域】 本發明涉及伸縮性優異並改善了後加工時製品穩定性 的捲曲的複合纖維及其製造方法。更詳細地說,涉及並列 型或偏心芯鞠型捲曲的複合纖維及其製造方法,該捲曲的 複合纖維具有高伸縮性,捲曲拉伸率大於等於4 〇 %、彈性 回復率大於等於70%,同時由於熱收縮應力的最高溫度大 於等於155°C,因此在織和染加工時,纖維對受熱過程和 張力非常穩定。 【先前技術】 ^專利文獻1中公開了使用兩種具有極限粘度差的聚對 苯一曱酸乙二酯(PET )的方法。另外專利文獻2和專利文獻 3中公開了使用普通的聚對苯二曱酸乙二酯和高收縮性的 共聚對苯二曱酸乙二酯製造具有潛在捲曲表現性的聚酯類 纖維,方法。此外,專利文獻4和專利文獻5中還提出了在 聚對苯二甲酸乙二酯(PET )中使用具有拉伸性的聚對二 甲酸丙二酯(PTT)或聚對苯二曱酸丁二酯(pBT)的方法。 但是,對於通過上述專利記載的現有的製造方法製造 的捲曲的伸縮性複合纖維來說,其用於後序步驟時/,豆 帛的縮小一般大於等於10%,並且即使在最終加工/尉 烫時也要發生大於等於3%的形態變形,這樣產生的問題^ ^,製品加工時,難以設定其條件,難以穩定縫製丄的尺 一般來說,纖維製品在織/染加工、熱固定以及熨烫 第8頁 200532061 五、發明說明(2) 呀要經文130〜190C熱過程和1〜2g/d的張力,製品對熱 的形態穩定性是決定製品品質的重要因素。所以,為了使 製品在熨燙時的形態變形最小,必須解決現有技術中熨燙 時產生大於等於3 %的形態變形的問題。 、本發明人等認識到加工布帛在熨燙時發生的收縮率與 纖維的熱收縮應力的最高溫度有密切的關係,進而知道使 熱收縮應力的最高溫度大於等於丨5 5它的情況下,加工布 帛在熨燙時的收縮率小於等於3%,最終製品的形態穩定性 優異。 。另外’專利文獻6對熱收縮應力的最高溫度小於等於 ^0 °C且熱收縮應力的最大峰值大於等於0· 20cN/dtex的伸 縮,複合纖維進行了描述,但沒有言及最終纖維製品形態 ,,性的效果。一般來說,與普通纖維相比,伸縮性纖維 製品對織/染加工、熱固定以及熨燙時的熱過程和張力敏 感’形態穩定性是個問題。這對製品染色的均一性、染加 工1地及縫製品的尺寸穩定性有重要的影響,一般以熨费 收縮率為標準,如果熨燙收縮率大於等於3%,則認為製品 的品質不好。 另外’現有關於伸縮性複合纖維的專利大體上僅涉及 由不同的聚酯高分子得到的複合紡絲,沒有言及構成複合 纖維的不同鬲分子聚合物自身的分子量對複合纖維物性的 影響。專利文獻4中,雖然提到了聚對笨二甲酸乙二酯 (PET)、聚對笨二曱酸丙二酯(PTT)、改性的PET和改性的 PTT的枯度不同,相應的物性也不同,但該專利也未提及200532061 V. Description of the invention (1) [Technical field to which the invention belongs] The present invention relates to a crimped composite fiber having excellent stretchability and improved product stability during post-processing, and a method for manufacturing the same. More specifically, it relates to a side-by-side or eccentric core-shaped crimped composite fiber and a manufacturing method thereof. The crimped composite fiber has high stretchability, a crimp elongation rate of 40% or more, and an elastic recovery rate of 70% or more. At the same time, because the maximum temperature of heat shrinkage stress is 155 ° C or more, the fiber is very stable to the heating process and tension during weaving and dyeing. [Prior Art] ^ Patent Document 1 discloses a method using two types of polyethylene terephthalate (PET) having a difference in limiting viscosity. In addition, Patent Document 2 and Patent Document 3 disclose a method for producing a polyester fiber having latent crimping performance by using ordinary polyethylene terephthalate and high-shrinkage copolyethylene terephthalate. . In addition, Patent Documents 4 and 5 also propose the use of stretchable polyethylene terephthalate (PTT) or polybutylene terephthalate in polyethylene terephthalate (PET). Diester (pBT) method. However, when the crimped stretchable composite fiber manufactured by the conventional manufacturing method described in the above-mentioned patent is used in subsequent steps, the reduction of tempeh is generally greater than or equal to 10%, and even in the final processing / welding At the same time, a deformation of 3% or more must occur, which causes problems. ^ It is difficult to set the conditions during the processing of the product, and it is difficult to stabilize the sewing rule. Generally speaking, fiber products are knitted, dyed, heat-fixed, and ironed. Hot page 8 200532061 V. Description of the invention (2) Yeah, the thermal process of Scripture 130 ~ 190C and the tension of 1 ~ 2g / d. The morphological stability of the product to heat is an important factor that determines the quality of the product. Therefore, in order to minimize the morphological deformation of the product during ironing, the problem of morphological deformation of 3% or more during ironing in the prior art must be solved. The inventors recognized that the shrinkage rate of the processing cloth during ironing is closely related to the maximum temperature of the thermal shrinkage stress of the fiber, and further know that when the maximum temperature of the thermal shrinkage stress is greater than or equal to 5 5 it, The shrinkage of the processed fabric during ironing is 3% or less, and the final product has excellent morphological stability. . In addition, 'Patent Document 6 describes the expansion and contraction of the maximum temperature of the heat shrinkage stress of ^ 0 ° C and the maximum peak value of the heat shrinkage stress of 0 · 20cN / dtex, but does not mention the final fiber product form. Sexual effect. Generally speaking, compared with ordinary fibers, stretchable fiber products are sensitive to thermal processes and tension during the weaving / dyeing process, heat fixing, and ironing, and their morphological stability is a problem. This has an important impact on the uniformity of the dyeing of the product, the dyeing process and the dimensional stability of the sewing product. Generally, the shrinkage rate of ironing is used as the standard. If the shrinkage rate of ironing is greater than or equal to 3%, the quality of the product is considered to be poor. . In addition, the existing patents on stretchable composite fibers generally only relate to composite spinning obtained from different polyester polymers, and do not mention the influence of the molecular weight of the different fluorene molecular polymers themselves on the physical properties of the composite fibers. In Patent Document 4, although it is mentioned that polyethylene terephthalate (PET), poly (trimethylene pivalate) (PTT), modified PET and modified PTT have different dryness, the corresponding physical properties It's different, but the patent doesn't mention it

200532061200532061

構成複合纖維的不同高分子的分子量。當然,通過馬克 豪音庫等式(Mark-Hawink equation),雖然可以從枯户 分子量的關係中推測出分子量,但是不能得到關於分^旦 分佈的信息。另外,專利文獻4中,提到了利用pTT之 里 或者PTT-PET、ΡΤΤ-ΡΒΤ等具有不同粘度差的兩種聚酯^聚 合物的伸縮性複合纖維,但這其中也沒有關於分子量及^ 子畺分佈的#息。而本發明人等發現了具有不同枯度差、 兩種聚自旨類聚合物的分子量、分子量分佈以及拉伸^熱= 定溫度是影響纖維熱收縮應力的最高溫度、伸縮特性以及 加工布帛在熨燙時的收縮率的因素,並設計了兩種聚八 的最佳分子量和最佳分子量分佈。 口 【專利文獻1】特開平1〇 —72732號公報 【專利文獻2】特開2〇〇〇 —328378號公報 【專利文獻3】特開平9_41234號公報 【專利文獻4】美國專利第3 6 7丨3 7 9號公報 【專利文獻5】特開平1 89923號公報 【專利文獻6】特開2〇〇2 —54〇3〇號公報 【發明内容】 本發明的目的是提供捲曲的複合纖維及其製造方法, 所述捲曲的複合纖維利用了可在工業上使用的可形成纖維 的高分子’其伸縮性優異,並且製品的形態穩定性優異。 因此’本發明人等為了滿足這樣的目的而進行了認真 仔細地研究’結果發現,利用同為可形成纖維的高分子,Molecular weights of the different polymers that make up the composite fiber. Of course, through the Mark-Hawink equation, although the molecular weight can be inferred from the molecular weight relationship of dry households, information about the denier distribution cannot be obtained. In addition, Patent Document 4 mentions the use of pTT or PTT-PET, PTT-PBT and other two kinds of polyester ^ polymers with different viscosity differences in stretchable composite fibers, but this does not include molecular weight and ^息 distributed # 息。 The inventors have found that the molecular weight, molecular weight distribution, and stretching of two polymers with different dryness differences are different. The heat = constant temperature is the highest temperature that affects the thermal shrinkage stress of the fiber, the expansion and contraction characteristics, and the processing fabric. Factors of shrinkage when ironing, and designed the best molecular weight and the best molecular weight distribution of the two poly-8. [Patent Document 1] Japanese Patent Application Laid-Open No. 10-72732 [Patent Literature 2] Japanese Patent Application Laid-Open No. 2000-328378 [Patent Literature 3] Japanese Patent Application Laid-Open No. 9-41234 [Patent Literature 4] US Patent No. 3 6 7丨 3 7 9 [Patent Document 5] Japanese Patent Application Laid-Open No. 1 89923 [Patent Document 6] Japanese Patent Application Laid-Open No. 2000-5430 [Abstract of the Invention] The object of the present invention is to provide a crimped composite fiber and In its manufacturing method, the crimped composite fiber uses a fiber-forming polymer that can be industrially used, which has excellent stretchability and excellent morphological stability of the product. Therefore, ‘the present inventors have conducted a careful and careful study in order to satisfy such an object’, and found that using a polymer that also forms fibers,

200532061 五、發明說明(4) 的差為5〇〇°〜7〇〇°°,且各分子量分佈指數 的伸縮性傷ί不同的可形成纖維的高分子製造的複合纖維 子旦乂你,還發現以數均分子量為1 0000〜2〇000且分 成ίΐΐϊ為1,5〜2.5的可形成纖維的高分子作為第ϊ i子量為i5m〜9gggg且分子量分佈指數為 由所过當1出成纖維的高分子作為第2成分’各聚合物 斤^第1成为和所述第2成分構成時,各聚合 烫時形態變形最小的最佳聚合物。聚合:;吏= 2 = t於等於5_時’難以發現原絲的捲曲拉伸率和 匕:ί牛:大於等於7〇000時的缺點是’纺絲溫度的 低了分子量,其作用不能體現,並且紡絲 效果進難以保證工藝性’胃分子量增強了收縮 效果進而導致熨爱收縮率不佳。另外,將分子量分佈指數 限定在1.5〜2. 5的原因是’分子量分佈指數如果小於 1· 5 ’則分子量分佈不易均勻,低分子量物質的可塑 =作用變得微乎其微,容易在玉序上產生問冑;而分子 量分佈指數大於2· 5時,分子量分佈變大,產生幾個聚合 物混合的效果,所以在將熱固定溫度提高到一定準以"上 日U士被ί板=的現象’最終導致難以提高熱收縮應 力的最南溫度,產生降低形態穩定性和伸縮性的。 ^另外,本發明人等還發現,對於分子量高的聚合物來 說,由於紡絲間的熱分解嚴重減少了分子量,進一步擴大 =量分佈’但t果使纺絲組件内聚合物炫融體的滯留 時間最小化,例如在小於等於5分鐘時’ π以最大程度地200532061 V. Description of the invention (4) The difference is 500 ° ~ 700 °, and the elasticity of each molecular weight distribution index hurts the composite fiber made of different fiber-forming polymers. Once you ’ve finished, It was found that a fiber-forming polymer having a number average molecular weight of 10,000 to 20,000 and divided into 1,5 to 2.5 was used as the first polymer, and the molecular weight distribution index was i5m to 9gggg. The polymer of the fiber is used as the second component. Each polymer is the best polymer with the smallest morphological deformation during the polymerization when the first component is composed of the second component. Polymerization:; = 2 = t is equal to 5_ 'It is difficult to find the curling elongation and dagger of the original yarn: 牛牛: When it is greater than or equal to 7,000, the disadvantage is' the molecular weight of the spinning temperature is low, its effect cannot Manifested, and the spinning effect is difficult to ensure the processability. The stomach molecular weight enhances the shrinkage effect and leads to poor shrinkage. In addition, the reason why the molecular weight distribution index is limited to 1.5 to 2.5 is that if the molecular weight distribution index is less than 1.5, the molecular weight distribution is not easy to be uniform, and the plasticity of the low molecular weight substance becomes minimal, and it is easy to cause problems in the jade order.而; When the molecular weight distribution index is greater than 2.5, the molecular weight distribution becomes larger, resulting in the effect of mixing several polymers, so when the heat fixing temperature is raised to a certain level, " the phenomenon of the last day U Shi was d == ' In the end, it is difficult to increase the southernmost temperature of the heat shrinkage stress, resulting in a decrease in morphological stability and stretchability. ^ In addition, the inventors have also found that for polymers with high molecular weight, the molecular weight is severely reduced due to thermal decomposition between spinnings, which further expands = volume distribution ', but the polymer in the spinning assembly is dazzled. The residence time is minimized, such as' π to a maximum of 5 minutes

200532061 五、發明說明(5) 發揮所述特性引起的物性和功能性。 作為本發明的另一個側面,已知 一 伸縮性複合纖維來說,其用於 聰:由熔融紡絲得到 般大於等於1〇%,並且即使在'///驟/ ’布帛的縮小一 生大於等於3%的形態變形,製σ力 《,熨燙時也要發 件,難以穩定縫製品的尺寸。::缱二難以設定其條 加工、熱固定以及褽烫時要經受⑽叫 ^織-200532061 V. Description of the invention (5) The physical properties and functional properties caused by the above characteristics are exerted. As another aspect of the present invention, it is known that a stretchable composite fiber is used in Satoshi: 10% or more obtained by melt spinning, and even if the shrinkage of the fabric is greater than a lifetime It is equal to 3% of the shape deformation, σ force, and it is necessary to send pieces when ironing. It is difficult to stabilize the size of the sewing product. :: 缱 二 It is difficult to set the strips. Processing, heat fixing, and scalding are subject to howling ^ woven-

Wd的張力,但製品的形態穩定 缩〜 必須控制熨烫收縮率小於等於3%。這種:::: : 縮應力的最高溫度有密切的關# 二、,維的,、、、收 度提高到大於等·。C的水關:時^ 定性優異。 们水干時,伸細性製品的形態穩 棬* ΐ ί ί發明製造的伸縮性複合纖維具有高伸縮性,其 Ρ拉伸率大於等於復,彈性回復率大於等於7()%,同時 ,收縮應力的最高溫度大於等於155t,所以最線加工布 帛:贺烫收縮率小於等於3%,並且後加工時的製品穩定性 :好通過減少在纺絲組件内聚合物的滯留時間,使分 =量的減少、原絲物性及伸縮性的降低最小化,從而與現 2原絲相比,根據本發明製造的複合纖維提高了熱收縮應 ?的最咼溫度’可以謀求後續工序中的製品穩定性。另 夕卜’ I^原絲的拉伸度大以及伸縮特性等優異,所以根據 發明製造的複合纖維可以適用於多種多樣的用途,例如 織物、緯編、經編等。 200532061Wd tension, but the shape of the product is stable. Shrinkage must be controlled to 3% or less. This kind of ::::: The maximum temperature of the shrinkage stress is closely related. Second, the dimensional ,,,, and yield are increased to greater than, etc. C's water off: time ^ excellent qualitative. When they are water-dried, the shape of the extensible products is stable. * Ϊ́ ί The stretchable composite fiber manufactured by the invention has high stretchability. Its P elongation is greater than or equal to, and the elastic recovery rate is greater than or equal to 7 ()%. The highest temperature of stress is equal to or greater than 155t, so the most processed fabric: shrinkage rate of less than or equal to 3%, and product stability during post-processing: Good by reducing the residence time of the polymer in the spinning assembly, so that the fraction = quantity The reduction of the physical properties and the reduction of the elasticity of the raw silk is minimized, so that the composite fiber produced according to the present invention improves the maximum temperature of the heat shrinkage stress compared with the existing two raw silks. . In addition, since the original yarn has high elongation and excellent stretchability, the composite fiber produced according to the invention can be applied to various applications such as fabrics, weft-knitting, and warp-knitting. 200532061

【實施方式】 本發明提供形態穩定性優異的伸縮性複合纖維,其日 使用兩種可熔融紡絲的可形成纖維的聚合物得到的,2 =熱收縮應力的最高溫度大於等於丨5 5 〇c,無載荷下彿次 处。理後的捲曲拉伸率大於等於4〇%,彈性回復率大於等於 ,由其製造的加工布帛的熨燙尺寸變化率小於等於、 另外,其特徵在於,其中一種聚合物是聚對苯二甲 ~酯,其數均分子量為1 0 0 0 0〜2 0 0 0 0,分子量分佈指2 二h 5〜2· 5 ;另一種聚合物為聚對苯二甲酸丙二酯,』I =分子量為15_〜9_Q,分子量分佈指數為155數 兩種聚合物的數均分子量的差為5〇〇〇〜7〇〇〇〇。[Embodiment] The present invention provides a stretchable composite fiber with excellent morphological stability, which is obtained by using two kinds of fiber-forming polymers that can be melt-spun on a daily basis. 2 = the maximum temperature of the heat shrinkage stress is equal to or greater than 5 5 〇 c. The Buddha is under no load. The crimp elongation after being processed is 40% or more, the elastic recovery rate is greater than or equal to, and the ironing dimensional change rate of the processing fabric made therefrom is less than or equal to one. In addition, it is characterized in that one of the polymers is polyparaphenylene terephthalate ~ Ester, whose number average molecular weight is 1 0 0 0 0 ~ 2 0 0 0 0, molecular weight distribution refers to 2 2 h 5 ~ 2 · 5; another polymer is polytrimethylene terephthalate, "I = molecular weight It is 15 ~ 9_Q, and the molecular weight distribution index is 155. The difference between the number average molecular weights of the two polymers is 5000 ~ 7000.

乙 2外,其特徵在於,其中一種聚合物是聚對苯二甲_ 酯,其數均分子量為ΐ〇θθ〇〜2〇〇〇〇,分子量分佈指凄 二二5〜I 5 ;另一種聚合物為聚對苯二甲酸乙二酯、聚f ::甲酸丁二酯或聚對笨二甲酸乙二酯共聚物,其 ywo,,,分子量分佈 5〜2 5,^ 種聚合物的數均分子量的差為5000〜70000。 另外優選其斷面形態為並列型或偏心芯鞘型。In addition to B2, it is characterized in that one of the polymers is poly (terephthalate), and its number average molecular weight is ΐθθθ〇 ~ 200,000, and the molecular weight distribution refers to 222-5 ~ I5; the other The polymer is polyethylene terephthalate, polyf :: butylene formate, or polyethylene terephthalate copolymer, and its ywo,, molecular weight distribution is 5 to 2, 5, the number of polymers The difference in average molecular weight is 5,000 to 70,000. The cross-sectional shape is preferably a side-by-side type or an eccentric core-sheath type.

另外’優選其捲曲直徑小於等於8mm。 的· Ϊ:、1本ί明提供形態穩定性優異的伸縮性複合纖辦 1仏方法,其包括如下步驟: (A)將兩種聚酯熔融,其中一種聚合物是聚對苯二甲 夂酯,八數均分子量為1 0000〜20000,分子量分佈名In addition, it is preferable that the crimp diameter is 8 mm or less. Ϊ: 1 This method provides a flexible composite fiber office with excellent morphological stability, which includes the following steps: (A) two types of polyester are melted, and one of the polymers is polyparaphenylene terephthalate Esters, octa-average molecular weight is 10,000 ~ 20,000, molecular weight distribution name

第13頁 200532061 五、發明說明(7) 數為1.5〜2.5 ;另一種聚合物為聚對苯二甲酸丙二酯,其 數均分子量為1 5 0 0 0〜9 0 0 0 0,分子量分佈指數為丨· 5〜 2. 5 ; (B )使所述炼融物通過紡絲組件,並控制其在紡絲組 件中的滯留時間小於等於5分鐘,然後以2 2 0 0〜5 0 0 〇米/分 鐘的紡絲速度進行收取,收取成並列型或偏心芯鞘型的複 合絲; (C)將收取的複合絲於85〜95 °C的溫度進行拉伸以及 在160〜220 °C的溫度進行熱固定。Page 13 200532061 V. Description of the invention (7) The number is 1.5 ~ 2.5; the other polymer is polytrimethylene terephthalate, and its number average molecular weight is 1 500 0 ~ 9 0 0 0, molecular weight distribution The index is 丨 · 5 ~ 2.5; (B) passing the smelt through the spinning assembly, and controlling its residence time in the spinning assembly to be less than or equal to 5 minutes, and then using 2 2 0 0 ~ 5 0 0 〇M / min spinning speed is collected, collected into parallel or eccentric core-sheath composite yarn; (C) the collected composite yarn is drawn at a temperature of 85 ~ 95 ° C and at 160 ~ 220 ° C The temperature is thermally fixed.

另外’本發明提供形態穩定性優異的伸縮性複合纖維 的製造方法,其包括如下步驟: (A)將兩種聚酯熔融,其中一種聚合物是聚對苯二甲 酸乙二酯,其數均分子量為1〇〇〇〇〜2〇〇〇〇,分子量分佈指 數為1.5〜2.5 ;另一種聚合物為聚對苯二甲酸乙二酯、 對苯二甲酸丁二酯或聚對苯二甲酸乙二酯共聚物,其數 分子量為1 50 0 0〜90 00 0,分子量分佈指數為15〜2.5 ; (Β)使所述熔融物通過紡絲組件,並控制其在紡絲組 件中的滯留時間小於等於5分鐘,然後以22〇〇〜5〇〇〇米/八 鐘的紡絲速度進行收取,收取成並列型或偏心芯鞘型的=In addition, the present invention provides a method for producing a stretchable composite fiber with excellent morphological stability, which includes the following steps: (A) melting two polyesters, one of which is polyethylene terephthalate, and the number is equal The molecular weight is 10000 ~ 2000, and the molecular weight distribution index is 1.5 ~ 2.5; another polymer is polyethylene terephthalate, butylene terephthalate or polyethylene terephthalate A diester copolymer having a number molecular weight of 150,000 to 90,000 and a molecular weight distribution index of 15 to 2.5; (B) passing the melt through a spinning module and controlling its residence time in the spinning module Less than or equal to 5 minutes, and then collected at a spinning speed of 2200 ~ 5000 m / eight minutes, charged into a side-by-side or eccentric core-sheath type =

jc)將收取的複合絲於85〜951的溫度進行拉伸以及 在160〜220 c的溫度進行熱固定。 八=外,本發明的伸縮性複合纖維的製造方法優選通: 。刀疋向拉伸/假撚工藝或紡絲直接拉伸工藝製造。jc) The collected composite yarn is drawn at a temperature of 85 to 951 and heat-fixed at a temperature of 160 to 220 c. Eight = except, the manufacturing method of the stretchable composite fiber of the present invention is preferably:. It is manufactured by knife-end drawing / false twist process or spinning direct drawing process.

第14頁 200532061 五、發明說明(8) 另外’優選所述拉伸溫度為85〜95 t,熱固定溫产為 160 〜22(TC。 另外,本發明提供加工絲,其由所述伸縮性複合纖 製造,撚數為150〜2000。 另外,本發明提供混纖絲,其是所述伸縮性複合纖維 =,伸度大於等於5〇%且彿水收縮率大於等於15%的 性原絲的混纖絲。 ^外,本發明提供含有所述伸縮性複合纖維的布帛。 維,ί =二時變形最小而具有伸縮性的複合纖 各高分子的特性及其可形成:維的高分子。關於 物材料以及利用該聚合材的^及製造方法,結合聚合 析方法 门的可形成纖維的高分子的特性及其分 對於本發明所用的 差在500 0〜700 00、|八nA S物,為了使數均分子量的 -個成分必須是數均分刀量丄:指數為U〜2.5 ’其中 指數為ι.5〜2 5,另二子篁為1 00 0 0〜20〇〇〇、分子量分佈 ^〇〇〇〇 ^ 所用的聚合物可以 合物和這4b物質的故&用工業上利用的聚酯、尼龍等聚 -物質的改性的聚合物等。此外,還可以使用聚 200532061 五、發明說明(9) ---- 烯擴’聚合物’㊆&這些聚合物有•高溫工序 尸4笙t ί的問題,所以很難實際應用。f以使用聚酯或 二二+ (σ 2和,些物質的改性的聚合物,其具體例子可 聚ί苯i:Ϊ對苯:Τ酸乙二酯、聚對苯二甲酸丙二酯、 甲酽=4 丁一酯等為代表的聚酯;這些聚酯被間苯二 66尼醇等改性的共聚物;以及以尼龍6、尼龍 性的妓f物等為ί表的尼龍;這些尼龍被間:甲苯胺等改 ㈣;聚:4’可以熔融成型的聚合物。 分子量:佈dm數ί !:,r°°°°〜2°°°°、 不是說確定了 j ^刀子篁分佈指數為1.5〜2.5,這並 =說=:=:L合物和另一個成分的聚合物, 2關…量二量為咖〜 的數平均分子量為丨 ’、、' n . 5的活,另一個聚合物 〜2.5即可。m也〜:000、分子量分佈指數為1.5 2_〇且分子例如,數均分子量為moo〜 甲酸乙二 佈指數為1. 5〜2 5的聚^骗里 00〜90〇〇〇且分子量分 聚對苯二甲酸丁』可以Λ聚對苯二甲酸兩二醋: 乙二酿"Ρ,只要、:ίί 也可以同為聚對笨二甲酸 和分子量分佈#數在太:彡色譜法得到的數均分子量的差 種類無關,其種的範圍内,則與聚合:ί 數均刀子置為moo〜20000且分子量分佈指^^明 第16頁 200532061 〜2. 5的聚合物稱為低分子量的高分子,而數均分子量為 ljOOO〜胃9000>0且分子量分佈指數為丨5〜2 5的聚合物稱為 南分子Ϊ的南分子。 這些聚合物採用人們熟知的本體聚合、溶液聚合、表 :聚合等進仃製造’本發明中作為對象的聚合物可以使用 =些方法中的任意方法製造的聚合物,特別優選本體聚合 :的熔融聚合或固體聚合製造的聚合物,這樣的聚 製造經費方面是有利的。 1 η η n 本發/月中,低分子量的高分子的分子量最低值設為Page 14 200532061 V. Description of the invention (8) In addition, it is preferable that the stretching temperature is 85 to 95 t, and the thermal fixed temperature production is 160 to 22 (TC. In addition, the present invention provides a processing wire, which is made of the stretchability. Manufacture of composite fibers with a twist count of 150 to 2000. In addition, the present invention provides mixed fiber filaments, which are the said stretchable composite fibers = sexual raw yarns having an elongation of 50% or more and a water shrinkage of 15% or more. In addition, the present invention provides a fabric containing the stretchable composite fiber. Dimensions of the polymer of the composite fiber with the least deformation at two times and the characteristics of the stretchable composite fiber and its formation: dimensional polymer About the material material, the manufacturing method using the polymer material, and the characteristics of the polymer that can form a fiber in combination with the method of polymer analysis and its characteristics, the difference between the polymer used in the present invention is 500 0 to 700 00, and eight nA S In order to make the number-average molecular weight of a component must be the number-divided amount, the index is U ~ 2.5 ', where the index is ι.5 ~ 25, and the other two are 100,000 ~ 200,000, molecular weight. Distribution ^ 〇〇〇〇〇 ^ The polymer used can be conjugated and these 4b substances Therefore, & industrially used polyester, nylon and other poly-substance-modified polymers, etc. In addition, poly200532061 V. Description of the invention (9) ---- olefin expansion 'polymers' ㊆ & These polymers have the problem of high temperature processes, so it is difficult to practically use them. In order to use polyester or two + + (σ 2 and some modified polymers, specific examples can be gathered. Benzene: terephthalic acid: polyesters such as polyethylene terephthalate, poly (trimethylene terephthalate), formazan = 4 butadiene, etc .; these polyesters are modified by m-xylylenediol, etc. Copolymers; and nylons such as nylon 6, nylon-like prostitutes; these nylons are modified by m-toluidine; poly: 4 'polymers that can be melt-molded. Molecular weight: cloth dm number! :, R °°°° ~ 2 °°°°, not to say that the distribution index of j ^ knife is determined to be 1.5 to 2.5, which does not say =: =: L compound and polymer of another component, 2 levels … The amount of the two is the number average molecular weight of the coffee is' ',,' n .5, the other polymer is only ~ 2.5. M is also ~: 000, molecular weight distribution index is 1.5 2_ And the molecule, for example, the number-average molecular weight is moo ~ ethylene formate index is 1.5 ~ 2 5 poly ^ cheli 00 ~ 90,000, and the molecular weight fraction polybutylene terephthalate can be Λ polyterephthalic acid Twenty-two vinegars: Ethyl alcohol " P, as long as,: ίί can also be the same as polyparaben and molecular weight distribution #Number in Tai: 彡 The number average molecular weight difference obtained by chromatography has nothing to do with the range of its species , And the polymerization: ί number average knife is set to moo ~ 20,000 and the molecular weight distribution means ^^ Ming page 16 200532061 ~ 2.5 polymer is called a low molecular weight polymer, and the number average molecular weight is ljOOO ~ stomach 9000 > A polymer with a molecular weight distribution index of 0 and 5 to 25 is called a south molecule. These polymers are manufactured using well-known bulk polymerization, solution polymerization, and table polymerization. The polymers to be targeted in the present invention may be polymers produced by any of the following methods. Bulk polymerization: melting is particularly preferred. Polymers manufactured by polymerization or solid polymerization are advantageous in terms of funding for such polymerizations. 1 η η n The minimum molecular weight of low molecular weight polymers is

’尚分子量的高分子的分子量最高值設為90000,其 、。製造分子量小於1 0000的聚合物對聚合方法本 4 1 ί疋沒有困難的。但是,將其製成片狀(或顆粒)的形 I,制於利用聚合物進行纖維化。分子量小於1 0 0 0 0的 κ π沾成片屑時,非常容易形成碎粉,難以製成具有均一 =门片屑。分子量大於9 0 0 0 0的話,難以採用熔融聚合 屑I,體聚合法製造,即使這是可以的,其製造時間也會 ^ 不僅在經濟上不利,並且由於必須過度地提高紡絲 现又而使熱分解降低了分子量,其作用不能體現。The highest molecular weight of a polymer with a low molecular weight is set to 90,000, and. There are no difficulties in producing polymers having a molecular weight of less than 10,000 versus polymerization methods. However, it is made into a sheet-like (or granular) shape I, and is produced by using a polymer for fibrillation. When κ π with a molecular weight of less than 1 0 0 0 becomes flakes, it is very easy to form crushed powder, and it is difficult to make it with uniform = door flakes. If the molecular weight is greater than 9 0 0 0, it is difficult to use the melt polymerization chip I and the bulk polymerization method. Even if this is possible, the manufacturing time will be not only economically disadvantageous, but also because the spinning must be excessively improved. The molecular weight is reduced by thermal decomposition, and its effect cannot be reflected.

八外’將分子量分佈指數限定為1· 5〜2· 5,這是因 低八I t量分佈指數如果小於1 · 5,分子量分佈太均勻, .I f物質自身可塑性的作用微乎其微,容易在工序上 門7€,而分子量分佈指數大於2·5時,分子量分佈變 言到^ ^幾個聚合物混合的效果,所以在將熱固定溫度提 ^ 定水準以上時,發生被熱板塑化的現象,最終導致Bawai 'limited the molecular weight distribution index to 1.5 · 2.5 ~ 2.5. This is because if the low eight I t amount distribution index is less than 1.5, the molecular weight distribution is too uniform. The process comes to 7 €, and when the molecular weight distribution index is greater than 2.5, the molecular weight distribution is changed to the effect of mixing several polymers, so when the heat-fixing temperature is raised above a certain level, plasticization by a hot plate occurs. Phenomenon

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降低形態穩定性和伸縮 難以提南熱收縮應力的最高溫度 性,所以不是優選的。 •本發明中的數均分子量和分子量分佈指數是將聚合 或製成的複合纖維溶解在六氟異丙醇(HFIp)中,利用iDecreased morphological stability and expansion and contraction It is difficult to raise the maximum temperature property of the heat shrinkage stress, so it is not preferable. • The number average molecular weight and molecular weight distribution index in the present invention are obtained by dissolving polymerized or prepared composite fibers in hexafluoroisopropanol (HFIp), and using i

Waters公司的咼溫用GPC設備,以聚苯乙烯為標準物制° 定數均分子量(Μη)和重平均分子量(Mw),從下式換八“ 量分佈指數(PDI)。 、刀十Water temperature company's GPC equipment uses polystyrene as a standard to make the number average molecular weight (Mη) and weight average molecular weight (Mw), and change the "quantity distribution index (PDI)" from the following formula.

PD I =Mw/Mn (2 )複合纖維的製造 為製造複合纖維而進行熔融紡絲時的聚合物的紡絲溫 度設定為比各聚合物熔融溫度高2〇〜70 °C的溫度。聚合物 的紡絲溫度比聚合物的熔融溫度高出的溫度小於2 〇 t時, 熔融不均勻而導致擠出機内壓力過度升高,進而降低作業 性,另外,還會發生製成的複合纖維的物性不均一等的問 題,所以不是優選的。另外,聚合物的紡絲溫度比聚合物 的熔融溫度高出的溫度大於7〇 °c,雖然聚合物的流動性得 到了改善,但存在聚合物發生熱分解等問題,所以不是優 選的。 可以使吐出的一個個纖維狀聚合物在紡絲喷頭的正下 方接合以獲取並列型斷面的複合纖維,另外,也可以在聚 合物通過分配板進入紡絲喷頭的同時使其接合,製造偏心 芯鞘型斷面的纖維。 另外,本發明人還發現,對於分子量高的聚合物來PD I = Mw / Mn (2) Production of composite fibers The polymer spinning temperature during melt spinning to produce composite fibers is set to a temperature which is 20 to 70 ° C higher than the melting temperature of each polymer. When the spinning temperature of the polymer is higher than the melting temperature of the polymer by less than 20 t, uneven melting results in an excessive increase in the pressure in the extruder, which reduces workability. In addition, the resulting composite fiber may also occur. The problem of uneven physical properties is not preferred. In addition, the spinning temperature of the polymer is higher than the melting temperature of the polymer by more than 70 ° C. Although the fluidity of the polymer is improved, there are problems such as thermal decomposition of the polymer, so it is not preferable. The discharged fibrous polymers can be joined directly below the spinning nozzle to obtain a composite fiber with a side-by-side cross section. In addition, the polymers can be joined while entering the spinning nozzle through the distribution plate. Fabrication of eccentric core-sheath cross section. In addition, the inventors also found that for polymers with a high molecular weight,

200532061 五、發明說明(12) 說’由於纺絲間的熱分解嚴重減少了分子量,進一 +把大 了分子量分佈’但如果使纺絲組件内聚合物熔融體^ ^留 時間最小化’例如小於等於5分鐘時,可以最大程度地發 揮所述特性引起的物性和功能性。 Λ 得到的複合纖維可以利用通常製造聚酯複合纖維時所 用的部分定向絲的拉伸/假撚工藝或紡絲直接拉伸工蓺進 行纖維化。 本發明的核心技術的構成要素是控制紡絲速度為2 2 〇 〇 :5500米/分鐘。其原因是,以小於22〇〇米/分鐘的纺絲速 度紡絲時,低速紡絲導致聚合物熔融體的吐出量減少,不 ,在經濟上是不利的,並且拉伸時,熱收縮率因拉伸比的 提高而上升,最終使熨燙時的收縮率大於等於3%, =品對熱的形態穩定性急劇下降。一般來說,在低纺絲 ίίΐ通過高倍拉伸形成的具有結晶的纖維對熱表現出高 ^' 另外,以大於等於5 〇 〇 〇米/分鐘的紡絲速度紡絲 =,兩種不同分子量的聚合物間不同的熱特性、物理特性 起、、方絲性降低,進而紡絲工序的穩定性下降,所以不是 優選的。 *千 q Μ个疋 A Μ ^ ^明另一個核心技術構成要素的特徵是通過部分定 "、申/叙撚工藝或紡絲直接拉伸工藝進行製造時,y 制拉伸溫度為85〜95t:、軌固η 時’控 溫度小於等於85心以度為160〜22(KC。拉伸 埶引耙的湖各J時難均勻拉伸,而大於等於95 °c時由 穩」Γί:度變大,紡絲時的工序性和其物性變得不 〜 …、定度小於等於16 〇時,熱收縮應力的最高200532061 V. Description of the invention (12) Said 'Due to the thermal decomposition between spinnings, the molecular weight has been severely reduced, and the molecular weight distribution has been increased', but if the polymer melt in the spinning assembly is minimized ^ ^ residence time, for example, less than When it is equal to 5 minutes, the physical properties and functional properties due to the above-mentioned characteristics can be maximized. The composite fiber obtained by Λ can be fiberized using a partially oriented yarn drawing / false twisting process or a direct spinning spinning process commonly used in the production of polyester composite fibers. The constituent element of the core technology of the present invention is to control the spinning speed to 2200: 5500 m / min. The reason is that when spinning at a spinning speed of less than 2200 m / min, low-speed spinning causes a decrease in the amount of polymer melt to be discharged. No, it is not economically disadvantageous, and the heat shrinkage rate during stretching As the stretching ratio increases, the shrinkage rate at the end of ironing is 3% or more, and the shape stability of the product against heat decreases sharply. In general, the low-spinning fiber formed by high-stretching crystalline fibers exhibits high heat resistance. In addition, spinning at a spinning speed of 5000 m / min or more =, two different molecular weights Different polymers have different thermal properties, physical properties, and square silk properties, and the stability of the spinning process is lowered, which is not preferable. * Thousands q Μ 疋 A Μ ^ ^ indicates that the characteristics of another core technology component is that when manufactured through partial quotation, application / spinning process or spinning direct drawing process, the drawing temperature of y is 85 ~ 95t: When the rail is fixed at η, the temperature is controlled to be less than or equal to 85 degrees and the degree is 160 to 22 (KC. It is difficult to stretch uniformly at each J of the lake where the rake is pulled, and it is stable when it is greater than or equal to 95 ° c. When the degree becomes larger, the processability and physical properties at the time of spinning become less ~…, when the degree is less than or equal to 160, the maximum heat shrinkage stress

第19頁 200532061Page 19 200532061

溫度小於等於1 5 5 °C,最終加工布帛在熨燙時織物發生高 收^ ’使製品的形癌穩定性不均勻,降低了最終製品的"*品 質,所以不是優選的。另外,熱固定溫度大於等於Mo它 時,發生嚴重塑化,減弱了工序性和各種物性,所以不H 優選的。 對於表現出捲曲性的現有的伸縮性複合纖維來說,其 問題在於,其用於後序步驟時,布帛的收縮一般大於等ς 1 〇%,並且即使在最終加工後,熨烫時也要發生大於等於 3%的形態變形,製品加工時,難以設定其條件,難以穩定 縫製品的尺寸。普通纖維製品—般在織/染加工、埶固定 以及褽烫時要經受丨3 0〜丨9 〇 t;熱過程和i〜2 g / d的^力, =發日:人發現製品的形態穩定性與纖維的熱收縮應力的 最冋溫度有始、切的關係,將熱收縮應力的最高 大於等於155°〇的水平時,製品的形態穩定性優異。 表1顯不根據本發明的制絲條件得到的纖維的 功能性。 實施例 下面,基於實施例更詳細地說明本發明。 是舉例說明本發明,並不構成對 下述實訑例 首先說明根據本發明的方法智、生沾拉人/民疋 物性評價標準及其測定方法。[化的接s型複合纖維的 (a)熱收縮應力的測定 在初始載荷為0· 5g/d、升溫速度為 用Kanebo公司的熱應力試驗機進行測定。>、、條件下,利 200532061 、發明說明(14) (b )數均分子量和分子量分佈的測定 將聚合物或製成的複合纖維溶解在六氟異丙醇(Η{?丨p) 利用美國Waters公司的高溫用Gpc設備,以聚苯乙’ 準物質測定數均分子量(Mn)和重均分子量(Mw),從下1 算分子量分佈指數(PD〖)。 式換 【式2】 PD I =Mw/Mn (c)捲曲拉伸率和彈性回復率的測定 為測疋作為貫施例製造的捲曲的複合 拉伸率和彈性回復率,進行下述操作。 纖維物性的捲曲The temperature is less than or equal to 1 5 ° C, and the final processing cloth has a high yield when ironing ^ ', which makes the shape and stability of the product uneven and reduces the " * quality of the final product, so it is not preferred. In addition, when the heat-fixing temperature is equal to or higher than Mo, severe plasticization occurs, and process properties and various physical properties are weakened. Therefore, H is not preferred. For existing stretchable composite fibers that exhibit crimpability, the problem is that when used in subsequent steps, the shrinkage of the fabric is generally greater than 100%, and even after the final processing, it is necessary to iron the fabric. Morphological deformation of 3% or more occurs, and it is difficult to set the conditions during product processing, and it is difficult to stabilize the size of the sewn product. Ordinary fiber products—generally subjected to weaving / dyeing processing, 埶 fixing, and scalding 丨 3 0 ~ 丨 9 〇t; thermal process and the force of ^ 2 g / d, = hair date: the form of the product found by people The stability and the maximum temperature of the heat shrinkage stress of the fiber have a relationship between the beginning and the cut. When the maximum heat shrinkage stress is 155 ° or higher, the product has excellent morphological stability. Table 1 shows the functionality of the fibers obtained according to the spinning conditions of the present invention. Examples Hereinafter, the present invention will be described in more detail based on examples. It is an example to illustrate the present invention, and does not constitute the following practical examples. First, the method, physical property evaluation standard and measuring method of the method according to the present invention will be described. ((A) Measurement of thermal shrinkage stress of s-type composite fiber) The initial load was 0.5 g / d and the temperature rise rate was measured with a Kanebo thermal stress tester. > Under the conditions, Lee 200532061, Description of the invention (14) (b) Measurement of number average molecular weight and molecular weight distribution Dissolve the polymer or composite fiber in hexafluoroisopropanol (Η {? 丨 p) Use The high-temperature Gpc equipment of Waters Company in the United States measures the number average molecular weight (Mn) and weight average molecular weight (Mw) with polystyrene 'quasi-substances, and calculates the molecular weight distribution index (PD 〖) from the next 1. [Formula 2] PD I = Mw / Mn (c) Measurement of curl elongation and elastic recovery rate To measure the composite elongation and elastic recovery rate of the crimp produced as an example, the following operations were performed. Fiber physical curl

—將纖維束在無載荷下浸潰在沸水中,浸潰3〇分鐘後, 於室,以上的溫度乾燥。施加〇 lg/d的載荷,2分鐘後解 除載f,放置10分鐘。將經過所述步驟的樣品在〇〇〇2g/d 的載何下放置2分鐘,然後測定此時的長度(L1)。對所述 樣品施加〇· lg/d的載荷,2分鐘後測定長度(L2)。此後解 除0. 1 g/d的載荷,2分鐘後,測定該時間點時的長度 (L3) ^通過下式算出捲曲拉伸率和彈性回復率。-The fiber bundle is immersed in boiling water under no load. After immersing for 30 minutes, it is dried in the chamber at the above temperature. A load of 0 lg / d was applied, and after 2 minutes, the load f was released and left for 10 minutes. The sample subjected to the above steps was left under a load of 002 g / d for 2 minutes, and then the length at this time (L1) was measured. A load of 0.1 g / d was applied to the sample, and the length (L2) was measured after 2 minutes. Thereafter, a load of 0.1 g / d was removed, and after 2 minutes, the length (L3) at the time point was measured. The curl elongation rate and elastic recovery rate were calculated by the following formula.

捲曲拉伸率(%)=〔(L2-Ll)/L2〕X 1〇〇 彈性回復率(%)=〔(L2-L3)/(L2-LI)〕〕X 1〇〇 (d)熨烫收縮率的測定 採用常規方法進行織和染加工後,基於KS K 0 5 58-2〇〇1,Α-1(幹熱熨燙法),測定熨燙收縮率。 (e)捲曲直徑的測定 隨機選取20個纖維,用光學顯微鏡測定自重下的捲曲Curl elongation (%) = [(L2-Ll) / L2] X 100. Elastic recovery rate (%) = [(L2-L3) / (L2-LI)]] X 100 (d) Measurement of Ironing Shrinkage After conventional weaving and dyeing processes, the ironing shrinkage was measured based on KS K 0 5 58-2001, A-1 (dry heat ironing method). (e) Measurement of crimp diameter: 20 fibers were randomly selected, and the crimp under its own weight was measured with an optical microscope.

第21頁 200532061Page 21 200532061

五、發明說明(15) 直徑,然後計算出其平均值。 實施例1 在捲曲的複合纖維的製造中,使用數均分子量(Mn)為 1 2632、分子量分佈指數(PDI)為22的聚對苯二甲酸乙二 醋和數均分子量(Μη)為19149、分子量分佈指數(pDi)為 2. 4的聚對苯二甲酸丙二酯,其重量比為5 . 5, =熔融複合紡絲設備,以圖2_(d)的偏心芯鞘型斷面,設 疋紡絲溫度為270。(:、紡絲速度為22〇〇米/分鐘、组件内滯 Γ夺=分鐘,製造單絲細度為3·4丹尼爾的聚醋複合纖 拉伸裝置將通過所述纺絲/卷取獲得的複合 η 造賦予了彈簧形狀捲曲的捲曲型伸縮性複合 2二C細度為2」丹尼爾。拉伸時的拉伸比?175、 拉伸》皿度為85 °C、熱固定溫度為丨6 〇 t,直社 原絲:織物表現出非常優異的伸縮特性和表1 實施例2 在捲曲的複合纖維的製造中,使用數均分子量(Mn)為 385为子量分佈指數(pDI)為21的聚對苯二 乙二 ^33522 ^ ^ ^ ^(PDD ^ 的熔H入本;甲酸丙二酯’纟重量比為5 : 5,利用現有 絲「絲設備,以圖2_(a)的並列型斷面,設定紡 間f絲速度為2_米/分鐘、組件内滞留時 利用直刀里拉’造早絲細度為3.4丹尼爾的聚酯複合纖維。 拉置將通過所述纺絲/卷取獲得的複合纖維 伸製&賦予了彈簧形狀捲曲的捲曲型伸縮性複合纖V. Description of the invention (15) Diameter, and then calculate the average value. Example 1 In the production of crimped composite fibers, polyethylene terephthalate having a number average molecular weight (Mn) of 1,263, and a molecular weight distribution index (PDI) of 22, and a number average molecular weight (Μη) of 19,149 were used. Polytrimethylene terephthalate with a molecular weight distribution index (pDi) of 2.4, and its weight ratio is 5.5, = melt composite spinning equipment, with the eccentric core-sheath section of Figure 2_ (d), set The reed spinning temperature was 270. (:, Spinning speed of 2200 m / min, internal lag of the module = min, and a polyester composite fiber drawing device with a monofilament fineness of 3.4 denier will be obtained by the spinning / winding The composite η is made of a spring-type curling stretchable composite that has a 2 C fineness of 2 "denier. The stretching ratio during stretching is 175, the stretching degree is 85 ° C, and the heat setting temperature is 丨6 〇t, straight yarn: The fabric exhibits very excellent stretch characteristics and Table 1. Example 2 In the production of crimped composite fibers, a number average molecular weight (Mn) of 385 is used as a sub-quantity distribution index (pDI) of Polyethylene terephthalate of 21 ^ 33522 ^^^^^ (PDD ^ melted into the present; propylene formate '纟 weight ratio is 5: 5, using the existing silk "silk equipment, as shown in Figure 2_ (a) Side-by-side cross section, set the spinning speed of the spinning room to 2 m / min, and use a straight knife to pull the polyester composite fiber with a fineness of 3.4 denier when staying in the package. The drawing will pass through the spinning / Reeled composite fiber drawn & crimp type stretchable composite fiber with spring shape crimp

200532061 五、發明說明(16) 維,其單絲細度為2. 1丹尼爾。拉伸 拉伸溫度為9〇。&lt;:、熱固定溫度為i 8 01:龙:m ,^ j ^ t«. ^ , ν;^Λ ° 在捲曲的複合纖維的製造中, 182U、分子量分佈指數(pDI)為21的^ 為 酯和數均分子量(Mn)為88245、分子量又佑广一 ·文乙一 1 6的奄f+笑-田缺工 刀千里刀佈指數(PDI)為 ?的九對本一曱酸丙二醋,《重量比為5 : 的熔融稷合紡絲設備,以圖2 —(a)的並列型 許— 絲溫度為285 °C、紡絲速度為38〇〇米/ °又疋、、 2 Γ二1 ::::、細度為3.4丹尼爾的聚醋複合纖維 述紡絲/卷取獲得的複合纖維 維,1 痄Μ Γ &amp;狀捲曲的捲曲型伸縮性複合纖 技 原 伸” 丹尼爾。拉伸時的拉伸比為u 伸,皿度為90 C、熱固定溫度為17(rc ,苴姓 絲和織物表現出非當俱里从仙μ &amp; ~果不於表1 :乂優的伸縮特性和形態穩定性。 貫施例4 在捲曲的複合纖維的製造中,使用數均分子量(μ 西H 量分佈指數(PDI)為2.2的聚對苯二甲酸乙 2 2^^ ^25984 ^ ^(PDI) ^ 的、一A、子本—甲酸丙二酯,其重量比為5 : 5,利用現古 絲溫,合紡絲設備,以圖2 —U)的並列型斷面,設定紡 間為8 5 c、纺絲速度為2 6 0 0米/分鐘、組件内滯留時 1為4为鐘’製造單絲細度為4.6丹尼爾的聚醋複合纖維。寻200532061 V. Description of the invention (16) dimension, the monofilament fineness is 2.1 denier. Stretching The stretching temperature was 90. &lt;: The heat-fixing temperature is i 8 01: Dragon: m, ^ j ^ t «. ^, ν; ^ Λ ° In the manufacture of crimped composite fibers, 182U and a molecular weight distribution index (pDI) of 21 ^ Nine pairs of n-benzyl monoacetate, malonyl acetate with a number-average molecular weight (Mn) of 88245, and a molecular weight of Yoshihiro Y. Wen-Yi, 16 + Xiao-Tian Quegong Knife Chili Cloth Index (PDI) is? << The melt-coupling spinning equipment with a weight ratio of 5: is shown in Fig. 2— (a) in a side-by-side type with a silk temperature of 285 ° C and a spinning speed of 3800 m / °. 1 ::::, a composite fiber dimension obtained by spinning / winding of a polyester composite fiber with a fineness of 3.4 denier, 1 μM Γ &amp; crimped crimp type stretchable composite fiber technical extension "Daniel. Pull The stretching ratio during stretching is u stretching, the plate temperature is 90 C, and the heat-fixing temperature is 17 (rc. The silk and fabric of the surname show inexperienced from the cents μ &amp; ~ the results are not as shown in Table 1: Stretching properties and morphological stability. Example 4 In the production of crimped composite fibers, a polyethylene terephthalate having a number average molecular weight (μ H H distribution index (PDI) of 2.2) 2 2 ^^ ^ 25984 ^ ^ (PDI) ^ , A, Koben—propylene formate, with a weight ratio of 5: 5, using the current ancient silk temperature, combined spinning equipment, with a side-by-side cross-section of Figure 2-U), set the spinning room to 8 5 c. Spinning speed is 2600 m / min, and the retention time within the module is 1 to 4 for the bell 'to produce a polyester composite fiber with a monofilament fineness of 4.6 denier.

第23頁 200532061 五、發明說明(17) 利用其他拉伸裝置將通過所述紡絲/卷 拉伸,製造賦予了彈菁形狀捲曲的捲卷曲取型獲二^ 維,其單絲細度為2. 8丹尼爾。拉伸時的伸1 口 〇 拉伸溫度為9Gt、熱固;^溫度為16(rc,1 =為U、 原絲和織物表現㈣常優異的伸縮特性和Ύ =表b 實施例5 仏L穩疋性。 在捲曲的複合纖維的製造中,使 1369Ϊ、分子量分佈指數(PDI)為2·2的聚對二子量^Mn)為 酯和數均分子量(Μη)為25984、分子量八佑一甲-夂乙一 2.2的聚對苯二甲酸丙4,其“^5佈指數⑽)為 的熔融複合紡絲設備,㈣—⑷的偏:鞘5,利用現有 定紡絲溫度為mt;、紡絲速度為2 600 &quot;/ i斷面,設 留時間為4分鐘,製造單絲細度為69丹尼2 件内滯 維。利用其他拉伸裝置將通過所述紡练/ 、Λ Sa複合纖 纖維拉伸,製造賦予了彈簧形狀捲曲的卷取獲j寻的複合 二::工細度购尼^拉伸時^ • 拉伸,皿度為9 0 c、熱固定溫度為丨6 〇。 定性。 彳申&amp;特性和形態穩 實施例6 在捲曲的複合纖維的製造中,使 測5、分子量分佈指數(?])1)為2 數=子量(Μη)為 …聚對苯二甲酸乙二醋,其重::二佈指數T為 αυ · 4,利用現有 200532061 五、發明說明(18) =熔融複合紡絲設備,以圖2_(b)的並列型斷面,設定紡 絲溫度為295 t:、紡絲速度為24〇〇米/分鐘、組件内滯留時 間為4分鐘,製造單絲細度為3. 4丹尼爾的聚酯複合纖維。 =用其他拉伸裝置將通過所述紡絲/卷取獲收的複合纖維 _裝&amp;賦予了彈簧形狀捲曲的捲曲型伸縮性複合纖 X其單絲細度為2.1丹尼爾。拉伸時的拉伸比為162、 Ϊ 、熱固定溫度為22(rc,其結果示於表1。 原絲^織物表現㈣常優異的伸縮特性和形態穩定性。 實施例7 在捲曲的複合纖維的製造中,使用數均分子量(m 西ϊ Λ、λ 數(PDI)為2.2的聚對苯二甲酸乙二 Z 2的被間苯二甲酸取获了 1 〇麼 ^ 醋,其重量比為代二聚對笨二曱酸乙二 以圖2-⑷的並列型斷…定見絲設備, ◦米/分鐘、組件内滯留時分為』二 J為3.4丹尼爾的聚醋複合纖維。利用 ^早將? 過所述紡絲/卷取獲得的複合纖維拉伸 = 形狀捲曲的捲曲型伸縮性複合纖 弹簧 尼爾。拉伸時的拉伸比為167、 為2#1丹 溫度為180°C,士果示於表1。店 度為9〇C、熱固定 異的伸縮特性和形㈣、定性。I絲和織物表⑽非常優 (實施例8) 在捲曲的複合纖維的製造中,使用數均分子量(Mn)為 第25頁Page 23, 200532061 V. Description of the invention (17) Using other drawing devices, the spinning / rolling is stretched to produce a roll-curling type that gives the elastic blue shape a curl shape to obtain 2 ^ dimensions, and the monofilament fineness is 2. Daniel. When stretched, it is stretched at a temperature of 9 Gt and thermoset; the temperature is 16 (rc, 1 = U, the yarn and the fabric exhibit the usual excellent stretch characteristics and Ύ = Table b Example 5 仏 L In the manufacture of crimped composite fibers, 1369 Ϊ, a polyparameter (Mn) of a molecular weight distribution index (PDI) of 2.2 was used as an ester, and the number average molecular weight (Μη) was 25,984. -Polyethylene terephthalate 4 of 夂 2.2, whose melt-spinning equipment is "^ 5 cloth index ⑽", ㈣-⑷ partial: sheath 5, using the existing fixed spinning temperature as mt; The speed is 2 600 &quot; / i cross section, the retention time is 4 minutes, and the monofilament fineness is 69 deniers. 2 pieces of internal lagging dimension. Using other drawing devices will be passed through the spinning / Λ Sa composite fiber The fiber is stretched to produce a composite coil that gives a spring-shaped curl to obtain the second compound :: work fineness when buying ^ when stretched ^ • stretched, the degree of dish is 90 ° C, and the heat-fixing temperature is 丨 60. Qualitative characteristics &amp; characteristics and morphological stability Example 6 In the production of crimped composite fibers, the measurement 5, molecular weight distribution index (?)) 1) is 2 = sub (Μη) is ... polyethylene terephthalate, its weight: the second cloth index T is αυ · 4, using the existing 200532061 V. Description of the invention (18) = melt composite spinning equipment, as shown in Figure 2_ (b) The cross section of the parallel type was set at a spinning temperature of 295 t :, a spinning speed of 2400 m / min, and a residence time in the module of 4 minutes to produce a polyester composite fiber with a monofilament fineness of 3.4 denier. = The composite fiber obtained through the spinning / winding is loaded with another drawing device_loading &amp; crimp type stretchable composite fiber with spring shape crimp X, the single-filament fineness is 2.1 denier. The draw ratio was 162, Ϊ, and the heat-fixing temperature was 22 ° C. The results are shown in Table 1. The raw silk ^ fabric exhibited excellent stretching properties and morphological stability. Example 7 In the manufacture of crimped composite fibers Using isophthalic acid with a number-average molecular weight (m Λ λ, λ number (PDI) of 2.2 Z 2 was obtained by isophthalic acid 100 ^ vinegar, and its weight ratio is substituted dimerization The side-by-side determination of ethylene dibenzate is shown in Fig. 2-… ... See the silk equipment, ◦m / min, when staying in the module It is a polyester composite fiber of 3.4 denier. The early use of the composite fiber obtained by the spinning / winding is drawn = a curled elastic composite fiber spring with a shape of a curl. The stretching ratio is 167, the temperature is 2 # 1, the temperature is 180 ° C, and the fruit is shown in Table 1. The store temperature is 90 ° C, and the heat shrinkage characteristics are different, and the shape and qualitative properties are very high. Excellent (Example 8) In the production of crimped composite fibers, the number average molecular weight (Mn) was used.

EH^HI 200532061 五 、發明說明(19) 1 5385、分子量分佈指數(PDI)為2. 2的聚對苯二甲酸 酯和數均分子量(Μη)為3369 1、分子量分佈指 ^ 一 2. 2的聚對苯二曱酸丁二酯,其重量比為5 : 5,利用現 的熔融複合紡絲設備,以圖2-(a)的並列型斷面,設*兄有 絲溫度為275 °C、纺絲速度為2400米/分鐘組件内睹 為4分鐘’製造單絲細度為3. 4丹尼爾的聚酯複合纖維:: 用其他的拉伸I置將it過所述紡絲/卷取收得的複 】 拉伸’製造賦予了彈簧形狀捲曲的捲曲型伸縮性人纖纖維 維’其單絲細度為2. 1丹尼爾。拉伸時的拉_伸比為丨 拉伸溫度為90 °C、熱固定溫度為18〇它,1妹 比較例1 m32在捲八曲Λ複//Λ的製造中,使用數均分子量(_為 H刀(PDI)為2.2的聚對苯二曱酸乙二 2ΜΛν/ΛΓ^16!50' 的熔融複人纺蜉:備一知’其重量比為5:5,利用現有 辞「广以圖2—(a)的並列型,面,設定紡 用其他的拉伸裝置將通過=二/爾卷的:广纖維。利 拉伸,製造賊早了 π雄 糸卷取獲得的複合纖維 維,豆單今細;^ f形狀捲曲的捲曲型伸縮性複合纖 拉伸溫轨”、爾。拉伸時的拉伸比為1.70、 表明原絲和織物中;:::。。,其結果示於表2。 、寺性月,、、、貝減小,形態穩定性不穩 200532061 五、發明說明(20) 定。 (比較例2 ) 在捲曲的複合纖維的製造中,使用數均分 (M,69卜分子量旦分佈指數(PDI)為22的聚對苯里二^酸為 乙一 g日和數均分子量(Mn)為244JJ、八旦 為2. 7聚對苯二甲酸丙二酯,其重量二里·刀盲數(PDi) 的熔融複合紡絲設備,以圖2 —⑷的偏:芯勒利用現八有 定紡絲溫度為265 °C、紡絲速度為15〇〜 斷面,設 留砗H AS八制4抑# 為500未/分鐘組件内的滯 Γ ! ί甘 ' 度為6·0丹尼爾的聚酯複合纖 維。利用其他的拉伸裝置將通過所 、’ 合纖維拉伸,製造賦予了彈等形狀卷取獲得的複 合纖唯,:ϋ r 捲的捲曲型伸縮性複 口 ^維其早絲細度為2.丨丹尼爾。拉伸時的 =、拉伸溫度為75t、熱固定溫度為“π干 穩=2。。表明原絲和織物中伸縮特性有一些減小態不 (比較例3 ) 1 曰m中’使用數均分子量Uro為 酉旨和數均分子量(Mn)為3〇68。、分子 f = ^甲k乙一 2· 6的聚對苯二甲酸 刀佈才日數(PDI)為 的炫融複合紡絲設備以圖2重”為5 : 5 ’利用現有 :間為8分’製造單絲細度為8.1丹尼爾的聚;m 利用其他的拉伸震置將通過所述纺絲/:取=的= 200532061 五、發明說明(21) 、:拉:,t造賦予了彈簀形狀捲 =,其單絲細度為2.8丹尸匕爾。拉 ^伸=^纖 拉伸溫度為8Gt、熱固;^溫度為 $伸比為2.90、 表明原絲和織物中伸縮特性有—些減小,示於表2。 (比較例4 ) 心不穩疋 在捲曲的複合纖維的製造中 1 5385、八羊署八你杜私〜 使用數均分子量(Μη)為 巧385刀子里田刀佈指數(PDI)為2 2的聚對苯 S曰和數均分子置(Μη)為31292、分子 2 R沾取斜贫-田減 刀千里刀佈指數(PD I )為 ==5紡。絲,圖2七)的並列型斷面,設定纺 Ϊ二』L:、: ίΓΪ為14°〇米/分鐘、組件内的滯留 時間^刀,製造早絲細度為6. 〇丹尼 利用其他拉伸裝置將通過所述紡絲/卷 复。合纖纖维 彈黃形狀捲曲的捲曲型伸縮:複合纖 =/早4、,、田度為2. 1丹尼爾。拉伸時的拉伸比為2, 9〇、 拉伸溫度為75T:、熱固定溫度為145t,其結果示於表2。 表明原絲和織物中伸縮特性有一些減小,形態 (比較例5) “ 在捲曲的複合纖維的製造中,使用數均分子量(Mn 1 3490、分子量分佈指數(PDI)為2· 2的尼龍6和數平均分; 量(Μη)為3 1 290、分子量分佈指數(?1)1)為28的聚對苯二 甲馱丙一 S曰,其重置比為5 : 5,利用現有熔融複合紡 設備,以圖2-(a)的並列型斷面,設定紡絲溫度為27〇 ^ 紡絲速度為1 40 0米/分鐘、組件内的滯留時間為8分,製造EH ^ HI 200532061 V. Description of the invention (19) 1 5385, Polyterephthalate with a molecular weight distribution index (PDI) of 2.2 and a number average molecular weight (Μη) of 3369 1. Molecular weight distribution refers to ^ -2. The weight ratio of polybutylene terephthalate of 2 is 5: 5. Using the existing melt composite spinning equipment, with the side-by-side cross-section of Fig. 2- (a), the temperature of the filament is 275. ° C, spinning speed of 2400 m / min. It takes 4 minutes to produce a polyester composite fiber with a monofilament fineness of 3.4 denier: It is passed through the spinning with other drawing 1 丹尼尔。 Stretched to receive the complex] stretch 'manufactured crimp-type stretchable human fiber fiber with spring shape crimping' its monofilament fineness is 2.1 denier. The stretching ratio at the time of stretching is: the stretching temperature is 90 ° C, and the heat-fixing temperature is 180 °. 1 girl comparative example 1 m32 is used in the production of Vol. 8 compound Λ compound // Λ, using a number average molecular weight ( _ Is a melted compound rayon of polyethylene terephthalate 2MΛν / ΛΓ ^ 16! 50 'with a H knife (PDI) of 2.2: prepare a known' its weight ratio is 5: 5. Based on the side-by-side type shown in Figure 2- (a), other spinning devices used for spinning are set to pass = 2 / Seoul roll: wide fiber. It is stretched and manufactured, and the composite fiber obtained by π male winding is rolled up earlier. Dimensions are fine; ^ f-shaped curled stretchable composite fiber drawing temperature rail ", Er. The drawing ratio when drawing is 1.70, indicating that in the original silk and fabric ;: The results The results are shown in Table 2. Month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month, year, month, month, month, month, month, month, month, month, month, month, month, month, month, month, month and month and month. (M, 69 Bu poly (p-phenylene terephthalate) with a molecular weight denier distribution index (PDI) of 22 is ethylene glycol, and the number average molecular weight (Mn) is 244JJ, and Baden is 2.7 , Its melting compound spinning equipment with a weight of 2 li · blade blind number (PDi) is shown in Fig. 2-⑷: Xyler uses the existing Hachijo spinning temperature of 265 ° C and the spinning speed of 15 ° ~ cross section It is assumed that the 砗 H AS 八 制 4 抑 # is the hysteresis in the 500-per-minute module! 甘 The polyester composite fiber with a degree of 6.0 denier. Using other drawing devices will pass the fiber Stretching, manufacturing the composite fiber obtained by coiling with a shape such as a bomb, and the like: ϋ r roll of a crimped stretchable compound mouth ^ the fineness of the early filament is 2. Daniel. When stretching =, stretching temperature It is 75t, and the heat-fixing temperature is "π dry stability = 2." It shows that there is some reduction in the stretch properties of the raw silk and the fabric (Comparative Example 3) 1 The use of the number average molecular weight Uro in m is the purpose and number average The molecular weight (Mn) is 3068. The molecular f = ^ a k k 2-6 poly-terephthalate knife cloth number of days (PDI) is shown in Figure 2 of the composite spinning equipment is 5: 5 'Using existing: 8 points' to make a monofilament with a fineness of 8.1 denier; m using other stretching vibrations will pass the spinning /: take = = = 200532061 V. Invention Ming (21), :: The t-shaped endowment gave the shape of the impeachment, and its monofilament fineness was 2.8 dagger. The drawing temperature was 8Gt, and the thermosetting temperature was $. The elongation ratio is 2.90, indicating that there are some reductions in the stretch properties of the raw silk and the fabric, which are shown in Table 2. (Comparative Example 4) Heart instability in the manufacture of crimped composite fibers ~ Use poly-p-phenylene with a number-average molecular weight (Μη) of Qiao385, Litian knife cloth index (PDI) of 22, and a number-average molecular unit (Μη) of 31292, and a molecule of 2 R. The thousand-mile knife cloth index (PD I) is == 5 spinning.丝, Figure 2-7) side-by-side cross-section, set spinning ΪⅡ "L:,: ίΓΪ is 14 ° 0 m / minute, the residence time in the module ^ knife, the fineness of the early filament is 6. 〇 丹尼 用Other drawing devices will pass through the spinning / winding. Synthetic fiber Elastic yellow shape curling type expansion and contraction: composite fiber = / as early as 4 ,,, the degree is 2.1 denier. The stretching ratio at the time of stretching was 2,90, the stretching temperature was 75T, and the heat-fixing temperature was 145t. The results are shown in Table 2. It shows that the stretch characteristics of the raw silk and fabric are slightly reduced, and the morphology (Comparative Example 5) "In the production of crimped composite fibers, a nylon having a number average molecular weight (Mn 1 3490 and a molecular weight distribution index (PDI) of 2.2" was used 6 and number average score; poly (p-phenylene terephthalate) S with a quantity (Μη) of 3 1 290 and a molecular weight distribution index (? 1) 1) of 28. Its reset ratio is 5: 5. The composite spinning equipment is manufactured with a side-by-side cross section as shown in Fig. 2- (a), the spinning temperature is set to 27 °, the spinning speed is 1,400 m / min, and the residence time in the module is 8 minutes.

200532061200532061

=絲細度為6. 0丹尼爾的聚酰胺/聚酯複合纖維。利用其他 =伸裝f將通過所述紡絲卷取獲得的複合纖維拉伸,製造 疮予了彈簧形狀捲曲的捲曲 合纖維,其單絲細 Λ;2·1/尼爾。拉伸時的拉伸比為&quot;〇、拉伸温度為 織物中溫度為i45t:,其結果示於表2。表明原絲和 鲕特性有一些減小,形態不穩定。 200532061 五、發明說明(23) 丽8 Ρ1ΖΤ (15385) ΡΒΤ (33691) 2.2/2.2 ! 寸 275 2400 5 1 § g 160 Ο ΓΊ CC 實施例7 ΡίιΤ (15385) CO-ΡΙΤΓ (23300) 2.2/2.2 寸 275 2900 00 5 § § σ\ rn o CN (N W施例6 ?EV (15385) Ρ1ΓΓ (31300) 2.2/2.1 υη Ο CN 2400 00 oc 1.62 g 220 oo Ο rn 〇 (^1 &lt;E W施例5 ΡΓ:Τ (13691) VET (25984) 2.2/2.2 m oo Γ\ 2600 s/c 1.70 Ο § 170 Ο Cn i W施例4 ΡΒΤ (12632) ΡΙΓΓ (25984) 2.2/2.2 寸 285 2600 00 1.70 § 160 | 卜 ο oo vr^ CO 签 —ΐ 丽了— ΡΓ:Τ (18211) ΡΊΤ (88245) 2.1/1.6 寸 285 3800 00 3.70 § o — fN g r4 &lt;Ε 貨施例2 PET (15385) ΡΤΤ (33522) 5 Η 寸 275 2600 00 00 1.70 g g Ό ΙΟ CN un ri 合格 貨施例1 ΡΗΤ (12632) ΡΓΓ (19149) 2.2/2.4 寸 270 2200 s/c 1.75 *r&gt; oo 160 OO wo ο Η 00 CO O rj 聚合物Λ(Μη) 浆台物B(Mw) PDI(A/B) 組件內滯留時問(分鐘) 紡絲溫度(t:) 紡絲速度(米/分Μ) 斷面形態&quot; 1 拉伸比 拉仲溫度(°c) 熱固定溫度(t:) 熱應力的最高溫度〇C) 捲曲直徑(mni) 捲曲拉i中率(%) 彈性回復率(%) 熨燙收縮率(%) 熨燙收縮率是否合格~ ^οτ-rls驰 _「、:f*£^&lt;lnKn‘li:i:lw&gt;lrM?iG 到鍟2;i]、· :o/s,到冢笤:s/s 二 第30頁 200532061 五、發明說明(24) 表2 比較例1 比較例2 比較例3 比較例4 比較例5 聚合物A(Mn) PET PET PET PET 尼龍6 (12632) (12691) (15805) (15385) (13490) 聚合物B(Mw) PTT PTT PET PBT PTT (16950) (24411) (30680) (31292) (31290) PDI(A7B) 2.2/2.4 2.2/2.7 2.6/2.6 2.2/2.8 2.2/2.8 組件內滯留時間 4 8 8 8 8 紡絲溫度(°C) 270 265 270 275 270 紡絲速度(米/分鐘) 2500 1500 1400 1400 1400 斷面形態υ S/S s/c S/S S/S S/S 拉伸比 1.70 1 2.85 2.90 2.90 2.90 拉渖溫度(°c) 75 75 80 75 75 熱固定溫度(°c) 145 140 150 145 145 熱應力的最高溫度(°c) 139 132 148 135 137 捲齒直徑(mm) - 10.0 12.0 12.0 12.0 捲曲拉伸率(%) 23 36 39 32 38 彈性回復率(%) 68 70 67 66 69 契烫收縮率(%) 3.5 4.0 3.7 1 3.9 1 4,2 熨燙收縮率是否合格2) 不合格 不合格 不合格 不合格 不合格= Polyamide / polyester composite fiber with a silk fineness of 6.0 denier. The composite fiber obtained by the spinning and winding is stretched by using other = stretching equipment f to produce a crimped composite fiber having a spring-shaped curl, and the monofilament is thin Λ; 2 · 1 / Niel. The stretching ratio during stretching is &quot; 0, and the stretching temperature is i45t: the temperature in the fabric is shown in Table 2. The results are shown in Table 2. It shows that the characteristics of the protofilament and oolitic are reduced, and the shape is unstable. 200532061 V. Description of the invention (23) Li 8 Ρ1ΤΤ (15385) PBT (33691) 2.2 / 2.2! Inch 275 2400 5 1 § g 160 Ο ΓΊ CC Example 7 ΡΙΤ (15385) CO-PITΓ (23300) 2.2 / 2.2 inch 275 2900 00 5 § § σ \ rn o CN (NW Example 6? EV (15385) Ρ1ΓΓ (31300) 2.2 / 2.1 υη Ο CN 2400 00 oc 1.62 g 220 oo Ο rn 〇 (^ 1 &lt; EW Example 5 ΡΓ: Τ (13691) VET (25984) 2.2 / 2.2 m oo Γ \ 2600 s / c 1.70 Ο § 170 Ο Cn i W Example 4 ΡΒΤ (12632) ΡΓΓ (25984) 2.2 / 2.2 inch 285 2600 00 1.70 § 160卜 ο oo vr ^ CO Signature—ΐ 丽 了 — ΡΓ: Τ (18211) ΡΊΤ (88245) 2.1 / 1.6 inch 285 3800 00 3.70 § o — fN g r4 &lt; Ε Goods example 2 PET (15385) ΡΤΤ ( 33522) 5 mm inch 275 2600 00 00 1.70 gg Ό ΙΟ CN un ri Qualified goods Example 1 Ρ1Τ (12632) ΡΓΓ (19149) 2.2 / 2.4 inch 270 2200 s / c 1.75 * r &gt; oo 160 OO wo ο Η 00 CO O rj Polymer Λ (Μη) Pulp B (Mw) PDI (A / B) Retention time in the module (minutes) Spinning temperature (t :) Spinning speed (m / min. M) Section shape &quot; 1 Stretch specific temperature (° c) heat Fixed temperature (t :) The highest temperature of thermal stress 0C) Crimp diameter (mni) Crimp rate (%) Elastic recovery rate (%) Ironing shrinkage (%) Is the ironing shrinkage acceptable? ^ Οτ- rls 驰 _ 「、: f * £ ^ &lt; lnKn'li: i: lw &gt; lrM? iG to 鍟 2; i], ·: o / s, to mound: s / s II.30th page 200532061 V. Description of the invention (24) Table 2 Comparative Example 1 Comparative Example 2 Comparative Example 3 Comparative Example 4 Comparative Example 5 Polymer A (Mn) PET PET PET PET Nylon 6 (12632) (12691) (15805) (15385) (13490) Polymerization B (Mw) PTT PTT PET PBT PTT (16950) (24411) (30680) (31292) (31290) PDI (A7B) 2.2 / 2.4 2.2 / 2.7 2.6 / 2.6 2.2 / 2.8 2.2 / 2.8 Retention time in the module 4 8 8 8 8 Spinning temperature (° C) 270 265 270 275 270 Spinning speed (m / min) 2500 1500 1400 1400 1400 Sectional shape υ S / S s / c S / SS / SS / S Stretch ratio 1.70 1 2.85 2.90 2.90 2.90 Pulling temperature (° c) 75 75 80 75 75 Heat fixing temperature (° c) 145 140 150 145 145 Maximum temperature of thermal stress (° c) 139 132 148 135 137 Coil diameter (mm)-10.0 12.0 12.0 12.0 Curl elongation (%) 23 36 39 32 38 Elastic recovery rate (%) 68 70 67 66 69 Iron shrinkage rate (%) 3.5 4.0 3.7 1 3.9 1 4,2 Whether ironing shrinkage rate is acceptable 2) Unqualified Unqualified Unqualified Unqualified

nS/S並列型、S/C :偏心芯鞘型 2)熨燙收縮率是否合格的標準:小於等於±3.0%nS / S side-by-side type, S / C: eccentric core-sheath type 2) Whether the standard of ironing shrinkage is acceptable: less than or equal to ± 3.0%

第31頁 200532061 圖式簡單說明 【圖式簡單說明】 圖1是本發明所用的伸縮性和後加工時形態穩定性優 異的捲曲的複合纖維的熱收縮應力分析圖。 圖2的(a)〜(d)是根據本發明製造的伸縮性和後加工 時形態穩定性優異的捲曲的複合纖維的斷面圖。Page 31 200532061 Brief description of the drawings [Simplified description of the drawings] FIG. 1 is a thermal shrinkage stress analysis chart of a crimped composite fiber excellent in stretchability and morphological stability during post-processing used in the present invention. Figs. 2 (a) to (d) are cross-sectional views of crimped composite fibers having excellent stretchability and morphological stability during post-processing produced according to the present invention.

第32頁Page 32

Claims (1)

200532061200532061 第33頁 200532061 六、申請專利範圍 (A) 將兩種聚酯熔融,其中一種聚合物是聚對苯二甲, 二酯,其數均分子量為1 0 0 0 0〜2 0 〇 〇 〇,八不旦八处酸乙 刀丁里刀^^指金々从 1. 5〜2· 5 ;另一種聚合物為聚對苯二甲酸丙二酯,发^為 分子量為1 5 0 0 0〜9 0 0 0 0,分子量分佈指數為丨.5〜2,5數均 (B) 使所述熔融物通過紡絲組件,並控制其在纺絲組件 的滯留時間小於等於5分鐘,然後以2 2 〇 〇〜5 〇 〇 〇米/八/ 紡絲速度進行收取,收取成並列型或偏心芯顆型的^ $的 絲; 设B (C )將收取的複合絲於8 5〜9 5 °C的溫度進行拉伸以及 〜220 °C的溫度進行熱固定。 160 7· 一種複合纖維製造方法,其包括如下步驟: (A) 將兩種聚酯熔融,其中一種聚合物是聚對苯二甲酸 二酯,其數均分子量為1 0 0 0 0〜20 0 0 0,分子量分饰指&quot;&quot;數乙 1 · 5〜2 · 5 ;另一種聚合物為聚對苯二曱酸乙二酯、聚對, 二曱酸丁二酯或聚對苯二曱酸乙二酯共聚物,其數均分$ 量為15000〜90000,分子量分佈指數為丨.5〜2.5 ; (B) 使所述炫融物通過紡絲組件,並控制其在紡絲組件中 的滯留時間小於等於5分鐘,然後以2 2 0 0〜5 0 0 0米/分鐘的 紡絲速度進行收取,收取成並列型或偏心芯鞘型的複合 絲; (C )將收取的複合絲於8 5〜9 5 °C的溫度進行拉伸以及在1 6 0 〜2 2 0 °C的溫度進行熱固定。 8·如申請專利範圍第6或7項所述複合纖維的製造方法, 其特徵在於,通過部分定向拉伸/假撚工藝或紡絲直接拉Page 33, 200532061 VI. Scope of patent application (A) Two types of polyesters are melted, one of which is poly (p-xylylene) terephthalate, and the diester has a number average molecular weight of 1 000 0 to 2 0 〇〇〇, Eight-bladed eight-bodied acetic acid slicing knife ^^ refers to gold tincture from 1.5 to 2.5; another polymer is polytrimethylene terephthalate, and the molecular weight is 1 500 0 ~ 9 0 0 0 0, the molecular weight distribution index is 丨. 5 ~ 2,5. Number average (B) Pass the melt through the spinning module, and control its residence time in the spinning module to be less than or equal to 5 minutes, and then take 2 2000 ~ 500m / eight / spinning speed to collect, ^ $ silk into side-by-side or eccentric core type; let B (C) will collect the composite yarn at 8 5 ~ 9 5 ° It is stretched at a temperature of C and heat-fixed at a temperature of ~ 220 ° C. 160 7 · A method for manufacturing a composite fiber, comprising the following steps: (A) melting two polyesters, one of which is a polyterephthalate and having a number average molecular weight of 1 0 0 0 0 to 20 0 0 0 , Molecular weight distribution refers to "number of ethylene 1 · 5 ~ 2 · 5; another polymer is polyethylene terephthalate, polypara, butylene diacetate or polyterephthalate Ethylene oxalate copolymer, the number of which is equal to 15,000 ~ 90,000, and the molecular weight distribution index is 丨. 5 ~ 2.5; (B) passing the dazzling melt through the spinning component, and controlling it in the spinning component The residence time is less than or equal to 5 minutes, and then collected at a spinning speed of 2200 to 5000 m / min, and collected into a side-by-side or eccentric core-sheath composite yarn; The filaments were stretched at a temperature of 8 5 to 9 5 ° C and heat-fixed at a temperature of 160 to 220 ° C. 8. The method for manufacturing a composite fiber according to item 6 or 7 of the scope of application for a patent, characterized in that it is directly drawn through a partially oriented drawing / false twist process or spinning 第34頁 200532061Page 34 200532061 伸工藝製造。 9 · 種加工絲,其特徵在於,其是由申請專利範圍第1項 所述^伸,性複合纖維製造的,撚數為15〇 ~2〇〇〇。 1 0 ·、種混纖絲,其是申請專利範圍第1項所述的伸縮性 複合纖維和拉伸度大於等於5 〇 %且沸水收縮率大於等於1 5 % 的高收縮性原絲的混纖絲。 1 一種布帛,其特徵在於,其含有申請專利範圍第1項 戶斤述的伸縮性複合纖維。Manufacturing process. 9 · A type of processed yarn, characterized in that it is made of the stretched and composite fiber described in item 1 of the scope of patent application, and the twist number is from 150 to 2000. 1 ·· A mixed fiber filament, which is a mixture of the stretchable composite fiber described in the first item of the patent application scope and a high-shrinkage raw yarn with a stretch degree of 50% or more and a boiling water shrinkage of 15% or more. Filaments. A fabric characterized by containing the stretchable composite fiber described in the first item of the patent application scope.
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