TW313595B - - Google Patents

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TW313595B
TW313595B TW084104174A TW84104174A TW313595B TW 313595 B TW313595 B TW 313595B TW 084104174 A TW084104174 A TW 084104174A TW 84104174 A TW84104174 A TW 84104174A TW 313595 B TW313595 B TW 313595B
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Taiwan
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patent application
item
fiber
hydrophilic
spinning
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TW084104174A
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Chinese (zh)
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Danaklon As
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    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4282Addition polymers
    • D04H1/4291Olefin series
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4391Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres
    • D04H1/43918Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres nonlinear fibres, e.g. crimped or coiled fibres
    • 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
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/04Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/70Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
    • D04H1/74Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being orientated, e.g. in parallel (anisotropic fleeces)
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/165Ethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53Polyethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/647Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Nonwoven Fabrics (AREA)

Description

A7 經濟部中夬橾準局買工消費合作社印製 313595 B7 五、發明説明(1 ) 發明領域 本發明係鼷於使用親水纺絲整理劑處理的可再溼潤可 熱黏合之聚烯烴糸合成纖维,其製法及由織維製備之非織 產物。 該等纖維適合製備於一次或較佳多次溼潤後仍可維持 大致可溼潤性之親水非继材料,例如用作即棄式尿布的頂 片或分布層。 發明背醫 使用各型大致疏水性合成纖維例如各種聚烯烴纖维生 產多種不同材料,但成品需要或多或少的親水程度。例如 某些衛生吸收產品,如即棄式尿布中之材料即為此例,其 中吸收產品之某些部分必須可運送及/或保有水液如尿液 或血液。 將聚烯烴纖维之疏水表面改成或多或少親水性可以多 種方式進行,典型地係利用各種「坊絲整理劑」於纗維生 產過程中施於纖维表面上進行。但此種經表面處理纖維之 共通問題為通常相當容易禊失親水性。例如聚丙烯「親水 缬維」,其中親水性利用坊絲整理劑提供,通常於單次溼 潤後喪失其親水性。當嫌雄必須於數次溼潤後仍維持某種 親水性時顯.然不合其望,例如即棄式尿布。 業界已知使用含聚矽氧化合物於纺絲整理劑,來維持 經坊絲整理劑處理纖維的親水性至某種程度。因此EP 0 4 10 48 5-A1 (對應於US 5,045 , 387)描逑經由於纖維或原 纖化薄膜表面施用界面活性劑組成物而對含疏水聚烯烴纖 本紙張尺度適用中國國家標準(CNS ) A4規格(210'〆297公釐) C*請先閲讀背面之注意事項再填寫本頁)A7 Printed 313595 B7 by the Ministry of Economic Affairs, Central Bureau of Commerce and Industry Consumer Cooperation Co., Ltd. V. Description of the invention (1) Field of the invention The present invention is based on a re-wettable and heat-bondable polyolefin synthetic fiber treated with a hydrophilic spinning finishing agent Dimension, its preparation method and non-woven products prepared by weaving. Such fibers are suitable for the preparation of hydrophilic non-continuous materials that can maintain approximately wettability after one or preferably multiple wettings, for example as a topsheet or distribution layer for disposable diapers. The inventor of the invention uses various types of substantially hydrophobic synthetic fibers such as various polyolefin fibers to produce a variety of different materials, but the finished product requires a more or less hydrophilic degree. For example, some hygienic absorbent products, such as the materials in disposable diapers, are examples of this. Some parts of the absorbent product must be transportable and / or retain water such as urine or blood. Changing the hydrophobic surface of polyolefin fibers to be more or less hydrophilic can be carried out in many ways, typically by applying various "Fang silk finishing agents" to the fiber surface during the production process. However, the common problem with such surface-treated fibers is that it is usually quite easy to lose hydrophilicity. For example, polypropylene "hydrophilic valvi", in which the hydrophilicity is provided by Fang silk finishing agent, usually loses its hydrophilicity after a single wetting. Obviously, it is undesirable when the male suspect must maintain a certain degree of hydrophilicity after several wets, such as disposable diapers. It is known in the industry to use polysilicone compounds in spinning finishing agents to maintain the hydrophilicity of the fibers treated by the finishing agent to a certain extent. Therefore, EP 0 4 10 48 5-A1 (corresponding to US 5,045, 387) describes the application of the surfactant composition on the surface of the fiber or fibrillated film to apply the Chinese national standard (CNS) to the paper standard of hydrophobic polyolefin fibers. ) A4 specification (210'〆297mm) C * Please read the notes on the back before filling this page)

經濟部中央標準局員工消费合作杜印製 313595 at B7 五、發明説明(2) 維或原纖化薄膜的非锄材料提供親水性之方法,該界面活 性劑組成物包括水溶性聚烷氧化聚二甲基矽氧烷與抗靜電 化合物及/或烷氧化三S麻酸甘油酯組合。 但使用例如EP 0 41Q 485-A1所述聚矽氧化合物處理 聚烯烴缬維有某些缺點。包含1)纖維表面的聚矽氧導致含 纖維之非織材料強度下降,2)纖維生產過程之生產問題, 因聚矽氧化合物容易導致蓬鬆的纖維束,3)難以捲曲及梳 理纖維,原因為聚矽氧化合物經常導致堪維/金羼摩擦力 低,4)聚矽氧化合物不容易被生物分解,结果例如淸潔潘 維生產設備後造成醆物廢棄問題,及5)聚矽氧化合物相當 貴。因此希望利用坊絲整理劑獲得疏水聚烯斑纖维之親水 表面性質,纺絲整理劑首先,含有親水化合物,但僅微溶 於水,故親水性質更永久;其次,不含或僅含極小鼉聚矽 氧,故可避免前述因聚矽氧造成非織物強度降低的缺點。 另一種對聚烯烴纖維提供永久親水性之方法,係於纖 維纺絲前將界面活性劑攙混於熔融聚烯烴。此種方法述於 US 4,578,414 (將溼潤劑攙混於軍一成分之聚烯烴)及EP 0 34 0 763-A1 (將界面活性劑攙混於聚烯烴,生成鞘與S 型雙成分纖維之鞘成分)。但此等方法比較界面活性劑僅 施用作表面處理方法,有其缺點為需要相當大量活性劑。 因界面活性劑比起纖維聚合物(聚烯烴如聚丙烯或聚乙烯 )相當貴,容易造成生產成本明顯增高。结果即使此種纖 維之親水性良好,但其價格相當貴導致用途受限制。此種 方法之另一考處點為,於糸統中依靠添加劑遷移經過聚合 本紙法尺度逍用中國國家標準(CNS ) A4規格(210X 297公釐) - 5 _ (*先閱讀背面之注意事項再填寫本頁)Du Printed 313595 at B7 by the consumer cooperation of the Central Bureau of Standards of the Ministry of Economy V. Description of the invention (2) A method of providing hydrophilicity to non-hoe materials of dimensional or fibrillated films. The surfactant composition includes water-soluble polyalkylene oxide polymers Dimethicone is combined with antistatic compounds and / or alkoxylated tris sesame glyceride. However, treating polyolefin valvi with polysilicone as described in EP 0 41Q 485-A1 has certain disadvantages. Including 1) the polysilicon on the surface of the fiber causes the strength of the nonwoven material containing the fiber to decrease, 2) the production problem of the fiber production process, the polysiloxane compound is easy to cause fluffy fiber bundles, 3) it is difficult to curl and card the fiber because Polysilicon compounds often lead to low friction of Kanwei / Jinge. 4) Polysilicon compounds are not easily decomposed by biosynthesis. As a result, for example, Jijie Panwei produces equipment that causes waste disposal, and 5) polysilicon compounds are equivalent expensive. Therefore, we hope to use the square silk finishing agent to obtain the hydrophilic surface properties of the hydrophobic polyolefin fiber. The spinning finishing agent first contains a hydrophilic compound, but only slightly soluble in water, so the hydrophilic property is more permanent; second, it contains no or only a very small amount Polysilicone can avoid the aforementioned disadvantages of non-fabric strength reduction caused by polysilicone. Another method to provide permanent hydrophilicity to polyolefin fibers is to mix surfactants into the molten polyolefin before spinning the fibers. This method is described in US 4,578,414 (mixing a wetting agent with a polyolefin of one component) and EP 0 34 0 763-A1 (mixing a surfactant with polyolefin to produce a sheath and S-type bicomponent fiber sheath ingredient). However, these methods compare that the surfactant is only used as a surface treatment method, and has the disadvantage that a relatively large amount of active agent is required. Because the surfactant is quite expensive compared to the fiber polymer (polyolefin such as polypropylene or polyethylene), it is easy to cause a significant increase in production costs. As a result, even though such fibers have good hydrophilicity, their price is quite expensive and their use is limited. Another point of consideration for this method is that it relies on the migration of additives through the polymerized paper method in the Shitong system. The Chinese National Standard (CNS) A4 specification (210X 297mm) is used-5 _ (* Please read the precautions on the back (Fill in this page again)

、1T 313595 A7 B7 五、發明説明(3) 物至纖維表面,溼潤時添加劑被部分去除,纖維表面恢復 至足夠添加劑濃度箱要若干時間,典型為數小時。同時, 換言之,添加劑有效表面濃度尚未達到前,纖維不具有期 望的親水性。 此等先前技術缺點可藉本發明解決*本發明提供一種 使用大體不含聚矽氧化合物或僅含極小量聚矽氧化合物之 坊絲整理劑生產可再溼潤親水聚烯烴缳維之方法。 發明^簡Μ捃示 一個態樣中,本發明係《於一種生產可棟理親水聚烯 烴系短缬維之方法,該短纖維Μ水或水液至少溼潤一次後 仍可大體維持親水性,該方法包括下列步驟: a. 對經纺絲的長繼維施用包括至少一種親水潤滑爾之第 一坊絲整理劑,第一纺絲整理劑之聚二有機矽氧烷含董基 於第一坊絲整ίΐ劑之活性成分含量至多為5%簠量比, b. 拉伸長缬維, c. 對拉伸後的長纖維施用包括至少一種陽離子抗靜電劑 之第二纺絲整理劑,第二坊絲整理劑之聚二有機矽氧烷含 量基於第二纺絲整理劑之活性成分含量至多為5%重量比 經濟部中央標準局員工消费合作社印製 (·請先閲讀背面之注意事項再填寫本頁) d. 捲曲長缵維, e. 乾煉長纖維,及 f. 切割長纖維獲得親水短纖維; 該親水短纖維係為5g的孅維樣品,其係使用K15 B/ain 梳理該纖維而予Μ製備且取自具有基重1Q g/ea之梳理缴 本紙張尺度適用中國國家標準(CNS ) A4规格(210X297公釐) A7 B7 313595 五、發明説明(4) 維網,該纖維槎品藉由EDANA推薦非織物吸收試驗(第 10.1-72號)所测得液體吸收時間至多一分鐘。 本發明之其他態樣係翮於根據此方法生產的缀維,由 此種纖維生產的親水非織物及此棰非織物之製法。 發昍:> 註細据沄 「聚烯烴糸J 一詞表示本發明之纖維係由聚烯烴或其 共聚物生產,包含等規聚丙烯均聚物*及其輿乙烯,1-丁 烯,4 —甲基-卜戊烯等之逢機共聚物,及不等密度之線性 聚乙烯,如高密度聚乙烯,低密度聚乙烯及線性低密度聚 乙烯。用來生產聚烯烴系纖維之熔體也可含有各種習知绻 維添加劑,如硬脂酸鈣*抗氧化劑,製程安定劑及顔料, 包含增艶劑及著色劑如TiOs等。 缴維可為單一成分或雙成分缬維,後者例如為鞘與芯 塱雙成分繼維,芯之位置為偏心(偏雛圓心)或同心(大 致位在圓心)。顰成分纖維典型含有一個鞘和一個芯,其 分別包括聚丙烯/聚乙烯,高密度聚乙烯/線性低密度聚 乙烯,聚丙烯逢機共聚物/聚乙烯,或聚丙烯/聚丙烯逢 機共聚物。 根據本發明製備之纖维為白色(未添加顔料)或有色 (添加顔料)。 纖維纺絲較佳使用習知熔體坊絲(亦名長坊)特別中 速度習知坊絲完成。習知坊絲包括二步驟式方法,第一步 软為擠壓熔體及真正坊絲纖维;第二步驟為拉伸經纺絲的 纖維;此乃與所謂的「短坊」相反,短纺為一步驟式方法 本紙張尺度逍用中國國家標準(CNS ) A4规格(210X297公釐) m· 1 II ί — ί m nn 1— m· , =1 I- - I n In ....... .....--I - J In 1 In _ (¼先閱讀背面之注意事項再填寫本頁) 經濟部中央標準局員工消费合作社印策 A7 313595 B7 五、發明説明(5) ,其中纖維於單一操作坊絲及拉伸。 ("先閲讀背面之注意事項再填寫本頁) 坊絲時,熔融纖維成分由各別擠壓機導引通過分布系 統並通過纺嘴之孔。然後擠壓出的熔體導引通«淬冷導管 ,於此處冷卻並藉空氣流固化,同時抽拉成長纖維,聚集 成束,典型為數百根纖維。淬冷導管後,纺絲速度典型至 少約2(3 0 n/fflin,更典型約400-2500 n/Min。固化後, 長孅維使用第一纺絲整理劑處理。典型係利用刺輥進行* 但其他糸統例如噴灑長纖維束或浸泡於坊絲整理劑也適合 0 長坊方法中,拉伸係採用所謂的離線拉伸或離線抽拉 ,如前述完全與纺絲方法分開進行。拉伸過程典型地包括 一糸列熱輥及熱空氣烘箱,其中同時拉伸許多長壤維束。 長纖維束首先通過一組輥,接著通過熱空氣烘箱,然後通 過第二組輥。熱辊及熱空氣烘箱二者之典型溫度約50-340 Ό,例如約70-13Qt!,溫度係根據纖維類別選擇,例如典 型地聚丙烯纗維為115-135^,聚乙烯纖維為95-105t:, 經濟部中央標準局員工消費合作社印裝 及聚丙烯/聚乙烯雙成分纖維為110-12ϋυ。第二組熱輥 速度比第一組更快,因此經加熱的長缳維束根據兩種速度 之比(稱為拉伸比或抽拉比)拉伸。也可使用第二烘箱及 第三組熱輥(二階段式拉伸),第三組辊速度比第二組更 快。此種例中拉伸比為最末與最初一組輥之速度比。同理 可使用額外多組輥及多儸烘箱。本發明纖維典型使用下述 拉伸比拉伸:約1.05:1至約6:1,例如聚丙烯纖維由1.05:1 至2:1,及聚丙烯纖維及聚丙烯/聚乙烯雙成分绻维由2:1 8 本紙張尺度適用中國國家標準(CNS ) Α4規格(21〇Χ:297公釐) 經濟部中央標準局員工消費合作社印製 A7 _!Z__ 五、發明説明(6 ) 至4.5:1,獲得適當细度*亦即約1-7 dt ex,典型約1.5-5 <11^又,更典型約1.6-3.4(^63[。 拉伸後,長纖維束使用第二坊綠整理劑,例如使用剌 輥或藉噴灌或浸泡處理。長纗維可於捲曲前選擇性加熱, 例如利用超熱或飽和水蒸汽加热,或紅外線加熱器等加熱 提高溫度並融化坊絲整理劑成分。坊絲整理劑成分之融化 較佳於捲曲機之前進行,但也可於捲曲機內部或陳後的乾 燥步驟進行。加熱及融化潤滑劑所需能源可來自長纖維束 本身,長缠維束於拉伸過程中已被加熱,或另外可如前述 ,來自水蒸汽或紅外輻射。 於捲曲機内摩擦(其又影響由灌維產生的纖維網內聚 力)可藉調整製程參數,特別捲曲所用填塞箱隔間壓力, 調整至某種程度。但僅可在某些範圍内可行*範画係由纺 絲整理劑組成界定。 拉伸後的纖維通常經變形(捲曲)對纖維提供「波浪 形」Μ便適合梳理。有效變形Μ及纖維中相當大置捲曲, 可在梳理櫬器獲得高速,例如連續梳理速度至少80 in/Min ,典型至少約100 n/min,許多例中至少150 n/min或甚 至 20 0 n/ ainM 上。 捲曲典型係使用所謂填塞箱進行。長纖維束利用一對 壓力輥導引入填塞箱内隔間,此處由於未在隔間內向前抽 拉,造成壓力/變成捲曲。捲曲程度可藉填塞箱前方輥壓 力,隔間內壓力及溫度,及長纖維束厚度控制。另外,長 纖維可藉噴射空氣流通過噴嘴,藉空氣费形。某些例中, 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) I · f +?τ C請先閲讀背面之注意事項再填寫本頁) 經濟部中央樣準局員工消費合作社印製 A7 _____B7_ 五、發明説明(7) 亦即用於非對稱雙成分纖維,可免除捲曲裝置,其原因為 加熱處理纖維釋放纖維張力,導致收縮,因而產生三度空 間自行捲曲。 本發明纖維典型變形至約5-15捲/c®,典型約7-12捲 /c® (捲數為纗維彎折數)之程度。 例如於填塞箱內纖維捲曲後,典型地藉加熱處理固定 地減少拉伸與捲曲過程後可能存在的張力,因而使變形更 為永久性。纖維之固定及乾煉為終產物親水性之重要因素 ,其原因為:耐久的親水效果部分與親水成分僅鑀慢溶解 於水有關。此等成分當以小量水,例如來自生產過程纖維 表面之殘餘水混合時更容易溶解,故要緊地必須盡可能去 除殘餘水。特別重要的,乾燥單元例如轉鼓乾燥器*烘箱 ,乾煉與熱固通道等之熱空氣分布均勻,其原因為如此導 致纖維內之水汽含量低且分布均勻,其又影響终產物親水 性之永久性,說明如前。殘餘水含董基於缠維重童較佳低 於2.0%,更佳低於1.5%重量比。孅維之固定與乾燥可同 時進行,典型方式係將長纖維束例如經由輸送帶從填塞箱 導引通過熱空氣烘箱。烘箱溫度依據鑛維組成而定,但顥 然低於纖維聚合物或(於雙成分繼維之例)低於低熔點成 分之熔點。固定遇程中*缬維進行结晶遇程,结晶遴程將 缕維「鎖定J於捲曲形,因而可使變形更為永久性。熱處 理也可從坊絲整理劑去除某種數量之水。長纖維依據壤維 類型等因素而定,典型地於90-130¾例如95-125t:範圃之 溫度乾煉。 本紙張尺度適用中國國家標準(CMS ) A4規格(210X297公釐) 10 (··請先閎讀背面之注意事項再填寫本頁), 1T 313595 A7 B7 5. Description of the invention (3) When the substance reaches the surface of the fiber, the additive is partially removed when wet, and it takes a few hours for the fiber surface to recover to a sufficient additive concentration tank, typically a few hours. At the same time, in other words, before the effective surface concentration of the additive has been reached, the fiber does not have the desired hydrophilicity. These shortcomings of the prior art can be solved by the present invention * The present invention provides a method for producing a rewetable hydrophilic polyolefin thread using a square silk finishing agent that is substantially free of polysiloxane or contains only a very small amount of polysiloxane. Invention ^ 简 M In one aspect, the present invention is "a method for producing short-valve dimensional hydrophilic polyolefins. The short fiber M water or water can still maintain its hydrophilicity after being wetted at least once. The method includes the following steps: a. Applying the first square silk finishing agent including at least one hydrophilic lubricating agent to the long-twisted dimension of the spinning, the polydiorganosiloxane containing the first spinning finishing agent based on the first square The content of active ingredients of the silk finishing agent is at most 5%, b. Stretching long valvi, c. Applying a second spinning finishing agent including at least one cationic antistatic agent to the long fiber after stretching, the first The content of polydiorganosiloxane in Erfang Silk Finishing Agent is based on the active ingredient content of the second spinning finishing agent. (Fill in this page) d. Crimp long thread, e. Dry long fiber, and f. Cut the long fiber to obtain hydrophilic short fiber; The hydrophilic short fiber is a 5g small dimension sample, which is carded with K15 B / ain The fiber is prepared from M and taken from a base with a basis weight of 1Q The standard of g / ea carding paper is applicable to China National Standard (CNS) A4 specification (210X297mm) A7 B7 313595 V. Description of invention (4) Dimensional net, this fiber product is recommended by EDANA for non-woven fabric absorption test (section No. 10.1-72) The measured liquid absorption time is at most one minute. Other aspects of the present invention are based on the embellishment dimension produced according to this method, the hydrophilic non-woven fabric produced from such fibers, and the method of making this non-woven fabric. Development: > Note that according to the word "Polyolefin Shi J" indicates that the fiber of the present invention is produced from polyolefin or its copolymer, including isotactic polypropylene homopolymer * and its ethylene, 1-butene, 4-Methyl-pentene copolymers such as opportunity copolymers, and linear polyethylenes of different density, such as high density polyethylene, low density polyethylene and linear low density polyethylene. Used to produce polyolefin fiber melt The body may also contain various conventional dimensional additives, such as calcium stearate * antioxidants, process stabilizers and pigments, including thickeners and colorants such as TiOs, etc. The payment may be a single-component or two-component valvi, the latter For example, the sheath and core are two-component relays, and the core position is eccentric (partially round center) or concentric (approximately at the center of the circle). The chopped fiber typically contains a sheath and a core, which include polypropylene / polyethylene, respectively. High-density polyethylene / linear low-density polyethylene, polypropylene copolymer / polyethylene, or polypropylene / polypropylene copolymer. The fibers prepared according to the present invention are white (without added pigment) or colored (added Pigment). It is done using Xizhi melt square silk (also known as Changfang), especially medium-speed Xizhifang silk. Xizhifang silk includes a two-step method, the first step is extruding melt and real silk fiber; second The step is to stretch the spun fiber; this is the opposite of the so-called "short square", short spinning is a one-step method. This paper scale uses the Chinese National Standard (CNS) A4 specification (210X297 mm) m · 1 II ί — ί m nn 1— m ·, = 1 I--I n In ....... .....-- I-J In 1 In _ (¼ Read the precautions on the back before filling in this Page) Employee Consumer Cooperative of the Central Bureau of Standards, Ministry of Economic Affairs, Printing Policy A7 313595 B7 V. Description of the invention (5), in which the fibers are drawn and drawn in a single workshop. (" Read the precautions on the back before filling in this page.) For Fangsi, the melted fiber components are guided by separate extruders through the distribution system and through the holes of the spinning nozzle. The extruded melt is then guided through the «quenching duct, where it is cooled and solidified by the air flow, and at the same time the long fibers are drawn and gathered into bundles, typically hundreds of fibers. After quenching the catheter, the spinning speed is typically at least about 2 (30 n / fflin, more typically about 400-2500 n / Min. After curing, the long-dimensional dimension is treated with the first spinning finishing agent. The typical process is to use a spur roller. * However, other systems such as spraying long fiber bundles or immersed in Fangsi finishing agent are also suitable. In the Fangfang method, the drawing system uses so-called offline drawing or offline drawing, which is completely separate from the spinning method as described above. The stretching process typically includes a series of hot rollers and a hot air oven in which many long soil dimensional bundles are drawn simultaneously. The long fiber bundles first pass through a set of rollers, then through a hot air oven, and then through a second set of rollers. The typical temperature of both air ovens is about 50-340 Ό, such as about 70-13Qt !, the temperature is selected according to the type of fiber, for example, the typical polypropylene fiber dimension is 115-135 ^, polyethylene fiber is 95-105t :, economic The printing and printing of polypropylene and polyethylene bicomponent fiber of the Ministry of Standards and Staff Consumer Cooperative is 110-12 ϋυ. The second group of hot rollers is faster than the first group, so the heated long ray beam is based on the ratio of the two speeds (Called stretch ratio or draw ratio Stretching. You can also use the second oven and the third group of hot rollers (two-stage stretching). The speed of the third group of rollers is faster than the second group. In this case, the stretching ratio is the last and the first group of rollers. Speed ratio. Similarly, additional sets of rollers and multiple ovens can be used. The fibers of the present invention are typically drawn using the following draw ratios: about 1.05: 1 to about 6: 1, for example, polypropylene fibers from 1.05: 1 to 2 : 1, and polypropylene fiber and polypropylene / polyethylene two-component yarn dimension from 2: 1 8 This paper scale is applicable to China National Standard (CNS) Α4 specification (21〇Χ: 297 mm) Employee consumption of the Central Standards Bureau of the Ministry of Economic Affairs A7 _! Z__ printed by the cooperative. V. Description of the invention (6) to 4.5: 1, to obtain appropriate fineness * that is about 1-7 dt ex, typically about 1.5-5 < 11 ^ again, more typically about 1.6-3.4 (^ 63 [. After stretching, the long fiber bundles are treated with a second square green finishing agent, such as using a roll or by sprinkling or dipping. Changwei can be selectively heated before crimping, such as using superheated or saturated steam Heating, or infrared heaters, etc. raise the temperature and melt the ingredients of the wire finishing agent. The melting of the wire finishing agent is better than curling It is carried out before, but can also be carried out in the drying step inside the crimping machine or after aging. The energy required for heating and melting the lubricant can come from the long fiber bundle itself, and the long-wrap dimension bundle has been heated during the stretching process, or it can be As mentioned above, it comes from water vapor or infrared radiation. The friction in the crimping machine (which in turn affects the cohesion of the fiber web produced by the irrigation and maintenance) can be adjusted to a certain degree by adjusting the process parameters, especially the pressure of the stuffing box compartment used for crimping, but only It is feasible in certain scopes * The painting is defined by the spinning finishing agent. The drawn fiber is usually deformed (crimped) to provide a "wavy" Μ to the fiber, which is suitable for carding. The effective deformation Μ and the fiber are quite large For curling, high speed can be obtained in the carding comb, such as continuous carding speed of at least 80 in / Min, typically at least about 100 n / min, in many cases at least 150 n / min or even 200 n / ainM. Crimping is typically done using so-called stuffing boxes. The long fiber bundle is guided into the compartment in the stuffing box by a pair of pressure rollers, where it is not drawn forward in the compartment, causing pressure / turning into curl. The degree of curling can be controlled by the pressure of the roller in front of the stuffing box, the pressure and temperature in the compartment, and the thickness of the long fiber bundle. In addition, the long fibers can be sprayed through the nozzles, and the air can be shaped. In some cases, this paper scale is applicable to the Chinese National Standard (CNS) A4 (210X297mm) I · f +? Τ C Please read the precautions on the back before filling this page) Employee Consumer Cooperative Printed A7 _____B7_ V. Description of the invention (7) It is also used for asymmetric bicomponent fiber, which can avoid the curling device. The reason is that the heat treatment fiber releases the fiber tension and causes shrinkage, which results in a three-dimensional space. The fibers of the present invention are typically deformed to the extent of about 5-15 rolls / c®, typically about 7-12 rolls / c® (the number of rolls is the number of dimensional bends). For example, after crimping the fibers in the stuffing box, heat treatment is typically used to fixedly reduce the tension that may exist after the stretching and crimping process, thereby making the deformation more permanent. The fixing and drying of fibers are important factors for the hydrophilicity of the final product. The reason is that the durable hydrophilic effect is partly due to the fact that the hydrophilic component only slowly dissolves in water. These components are easier to dissolve when mixed with a small amount of water, such as residual water from the fiber surface of the production process, so it is important to remove the residual water as much as possible. Of particular importance, the hot air in drying units such as drum dryers *, drying and thermosetting channels is evenly distributed. The reason is that the moisture content in the fiber is low and the distribution is even, which affects the hydrophilicity of the final product Permanent, as stated above. The residual water content is preferably less than 2.0%, and more preferably less than 1.5% by weight based on the weight of the heavyweight. Fixing and drying can be performed at the same time. The typical way is to guide the long fiber bundle from the stuffing box through a hot air oven, for example, through a conveyor belt. The temperature of the oven depends on the composition of the mineral dimension, but it is lower than the fiber polymer or (in the case of two-component secondary dimension) lower than the melting point of the low melting point component. During the fixation process, the valium undergoes the crystallization process. The crystallization process locks the dimensional dimension to the curl shape, which can make the deformation more permanent. Heat treatment can also remove a certain amount of water from the square silk finishing agent. The fiber depends on the type of soil dimension and other factors, and is typically dried at 90-130¾, such as 95-125t: Fanpu temperature. The paper size is applicable to the Chinese National Standard (CMS) A4 specification (210X297 mm) 10 (·· please (Read the notes on the back before filling this page)

經濟部中央標準局舅工消費合作社印製 Α7 Β7 i、發明説明(8 ) 然後,經固定與乾燥的長纖維束導引至切割機,此處 纖维被切割成期望長度之短纖維。切割典型地係將纖維通 過内含徑向設置刀之輪進行。纖維利用輥之壓力壓住刀片 ,然後切成所需長度。等於刀與刀間距雜。本發明纖維典 型地切成長約18-150 M,更典型約25-1QQ nm,特別約30 -65 μ之短纖維,根據梳理設備及纖維细度而定。長度約 38-40 適合细度約2.2 dtex之纖維,長度45-50 μ適合 3 . 3 dtex缴維。 概略而言,坊絲及拉伸聚合物纖維用之纺絲整理劑之 主要要求包括下列: 1. 需含定量抗靜電劑,Μ確保缴維於坊絲與拉伸過程或 梳理過程不會帶電;陰離子、陽雔子及非離子抗靜m劑均 可用於坊絲整理劑,κ及兩性化合物及鹽也可使用。 2. 若有所滯,褥含定量內聚力提供劑俾確保長纖維維持 成束,可使其加工不會糾结;中性植物油,長鐽酵,醚及 酯,肌酸酐及非離子界面活性劑常用於此目的。 3. 餺含生產過程中可調整纖維/纖維及纖維/金屬摩擦 力成分,故長钃維於製程中不會被磨耗或磨斷。特別纺絲 階段之纖維/金饜摩擦,纖維/金屬摩擦拉伸輥,及於捲 曲器纖維/纖維及纖維/金屬摩擦需加調整。 4. 通常需要水加乳化劑或界面活性劑Μ維持各成分於水 溶液中之或多或少水溶性。 坊絲整理劑也用來調整桷理過程之缠維/缠維及纖維 /金靨摩擦,及通常採用用於纺絲及拉伸之纺絲整理劑, 本紙張尺度適用中國國家標準(CNS ) Α4規格(210 X 297公釐) -1 1 - 1:,--^------^ ..ΪΤ^ (·請先閲讀背面之注意事項再填寫本頁) 313595 五、發明説明(9) 因此缬維於梳理前無需進一步加工。 抗靜電劑為聚烯烴纖維生產所用坊絲整理劑全部皆需 要的成分。Μ下通常抗靜電成分之典型數值作為其抗靜電 性相對效率指南:無櫬鹽1GQ,陽雛子80-10(1,陰離子7 5-90,非雛子50-70,固定劑30,礦油及聚矽氧0-10,潤滑 劑30-50。已知陽離子抗靜電劑比陰離子更有效,因此適 當陽離子抗靜電劑可使用遠更低濃度。 本發明係基於用於纺綠及拉伸步驟二者之坊絲整理劑 其可滿足上列有關抗靜電劑及親水潤滑劑含量需求,Μ及 調節纖维/纖維及纖維/金属摩擦。纺絲整理劑之進一步 優點為可於梳理過程中作為加工助劑,因此提供獲得提供 充分梳理所需的缠維/纖維及纖維/金鼷摩擦。结果即使 使用相對高的梳理速度也可獲得纖維分布均勻的梳理網。 經濟部中央揉準局員工消費合作杜印製 (丨請先閲讀背面之注意事項再填寫本頁) 先前技術坊絲整理劑之ΡΗ (包括醸胺糸隈離子抗靜霉 劑或脂肪酸醸胺縮合物)通常略為酸性,典型低於pH 4。 此等情況下,釀胺氮經常被質子化,因此可作為陽離子抗 靜電劑。可能此種質子化作用也可促成分散液更安定。然 而於較高pH值如5-6時,釀胺基不被質子化,因此釀胺不 具陽離子性。用於是否剌激皮濟不要緊之用途,例如用於 毛氈潘維之技術用途,此等醢胺經常使用低pH。另外也與 低PH經常可避免微生物生長,減少坊鏃品可能因氣體褪色 變色有覼。 但供本發明之用,本發明係關於用於衛生吸收產品例 如即棄式尿布之纖維,故要緊地必須避免因pH值過低引起 本紙張尺度適用中國國家揉準(CNS ) A4规格(210 X 297公釐) -12 - 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(10 ) 皮廣剌激。因此用於生產本發明纖維之纺絲整理劑之pH相 當高Μ避免酸誘發皮虜剌激。若需要若干酸來安定乳疲或 分散液*則較佳使用乙酸或其他揮發性酸,酸於拉伸過程 乾燥步驟中至少部分揮發,使整理後纖維塗膜之ΡΗ夠高可 避免酸誘生皮满剌激(酸揮發*導致pH由纺絲整理分散液 之4或以下提高至纖維上乾塗膜約5-6)。 因此,本發明之陽雛子抗靜甯劑必須具有PH (於10% 水溶液)不低於4.0。更佳pH不低於4.5,例如4.5-6.5, 如 5.0-δ·β ° 根據本發明所用隔雛子坊絲整理劑成分之特殊優點係 顒於聚烯烴,特別聚丙烯藉長坊技術加工過程中表面變成 部分氧化。如此,雖已知聚烯烴為疏水性,為某些情況下 可有非嚴格疏水性之表面性質。由於此種部分氧化结果, 若干羥基及羧基Μ及醛基及醣基被引導至表面上。氧化位 置具有陰離子特性,表示原則上排斥任何企圖施用於缅維 上的陰離子成分水溶液。结果導致纖維表面塗膜不均勻, 較無效,因此纖維有親水性不耐久Μ及梳理過程中沈積於 設備上的缺點。 本發明之陽離子坊絲整理劑(亦即於前述pH範圍)對 長纖維之親和性對糸統之永久親水性提供正貢獻。長缠維 與坊絲整理劑陽離子成分間產生之鍵结(參見下文有闞纖 維/長纖維表面之分解)並非共價鍵,但具有離子性質因 .此非永久性,特別當隨後纖維水或水液接觸時尤為如此。 然而根據本發明,當此種纖維表面與親水坊絲整理劑間之 本紙浪尺度適用中國國家揉準(CNS ) Μ规格(210 X 297公嫠) -13- (請先閲讀背面之注意事項再填寫本頁)Printed by Uncle Consumer Cooperative of Central Bureau of Standards, Ministry of Economic Affairs Α7 Β7 i. Description of invention (8) Then, the fixed and dried long fiber bundles are guided to a cutting machine, where the fibers are cut into short fibers of the desired length. Cutting is typically done by passing the fiber through a wheel with a radially arranged knife. The fiber is pressed against the blade by the pressure of the roller and then cut to the required length. It is equal to the distance between the knife and the knife. The fibers of the present invention are typically cut to lengths of about 18-150 M, more typically about 25-1QQ nm, especially about 30-65 μ, depending on the carding equipment and fiber fineness. The length of about 38-40 is suitable for fibers with a fineness of about 2.2 dtex, and the length of 45-50 μ is suitable for 3.3 dtex payment. In summary, the main requirements for spinning finishing agents for square yarns and drawn polymer fibers include the following: 1. Need to contain a certain amount of antistatic agent, M to ensure that the payment is not charged in the square yarn and the drawing or carding process ; Anion, catfish and non-ionic anti-static agent can be used in Fangsi finishing agent, κ and amphoteric compounds and salts can also be used. 2. If there is a lag, the mattress contains a quantitative cohesiveness providing agent to ensure that the long fibers remain bundled, so that their processing will not be entangled; neutral vegetable oils, long fermentation, ethers and esters, creatinine and nonionic surfactants Commonly used for this purpose. 3. 馎 contains adjustable fiber / fiber and fiber / metal friction components during the production process, so the long dimensional dimension will not be worn or broken during the manufacturing process. In the special spinning stage, the fiber / gold friction, the fiber / metal friction drawing roller, and the fiber / fiber and fiber / metal friction of the curler need to be adjusted. 4. It is usually necessary to add emulsifier or surfactant M to maintain the water solubility of each component in the water solution. Fang silk finishing agent is also used to adjust the entanglement dimension / entanglement dimension and fiber / golden friction in the alkaning process, and is usually used in spinning and drawing spinning finishing agent. This paper scale is applicable to China National Standard (CNS) Α4 specifications (210 X 297 mm) -1 1-1 :,-^ ------ ^ ..ΪΤ ^ (Please read the precautions on the back before filling this page) 313595 V. Invention description ( 9) Therefore, no further processing is required before the carding. Antistatic agents are all components required for the finishing agent of polyolefin fibers. The typical values of the usual antistatic ingredients under Μ are used as a guide to the relative efficiency of their antistatic properties: no salt 1GQ, yang chizi 80-10 (1, anion 7 5-90, non-chichi 50-70, fixative 30, mineral oil and Silicone 0-10, lubricant 30-50. It is known that cationic antistatic agents are more effective than anions, so appropriate cationic antistatic agents can be used at much lower concentrations. The present invention is based on the second step of spinning green and stretching The square silk finishing agent can meet the requirements of antistatic agent and hydrophilic lubricant content listed above, M and adjust the friction of fiber / fiber and fiber / metal. The further advantage of spinning finishing agent is that it can be used as a processing in the carding process Auxiliary agent, so it provides the entanglement / fiber and fiber / gold friction required to provide sufficient carding. As a result, even with a relatively high carding speed, a carding net with uniform fiber distribution can be obtained. Employee consumption cooperation of the Central Kneading Bureau of the Ministry of Economic Affairs Du Yinzhu (丨 Please read the precautions on the back before filling this page) The pH of the prior art square silk finishing agent (including the amine antibacterial agent or fatty acid amide condensate) is usually slightly acidic, typically below pH 4. Under these circumstances, amine nitrogen is often protonated, so it can be used as a cationic antistatic agent. Perhaps this protonation can also contribute to the stability of the dispersion. However, at higher pH values such as 5-6, The amine group is not protonated, so the amine is not cationic. It is used for applications that do not irritate the skin, such as for the technical use of Felt Panwe. These amines often use low pH. In addition, they can also be used with low pH. To avoid the growth of microorganisms and reduce the appearance of Fang Sao products due to the discoloration and discoloration of the gas. But for the purpose of the present invention, the present invention relates to fibers used in hygienic absorbent products such as disposable diapers, so it must be avoided that the pH is too low This paper standard is applicable to the Chinese National Standard (CNS) A4 specification (210 X 297 mm) -12-A7 B7 printed by the Employee Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs V. Description of the invention (10). The pH of the spinning finishing agent used to produce the fiber of the present invention is relatively high to avoid acid-induced skin stimulation. If several acids are needed to stabilize milk fatigue or dispersion *, it is preferred to use acetic acid or other volatile acids. At least part of the volatilization in the drying step of the drawing process, so that the PH of the fiber coating film after the finishing is high enough to avoid acid induced skin full stimulation (acid volatilization * causes the pH to increase from 4 or below of the spinning finishing dispersion to the dry coating film on the fiber About 5-6). Therefore, the anti-jingning agent of the present invention must have a pH (in a 10% aqueous solution) of not less than 4.0. More preferably, the pH is not less than 4.5, such as 4.5-6.5, such as 5.0-δ · β ° The special advantages of the silk finishing agent composition used in the present invention are due to the polyolefin, especially the surface of the polypropylene becomes partially oxidized during the processing by the Changfang technology. Thus, although the polyolefin is known to be hydrophobic, it is certain There may be non-strictly hydrophobic surface properties. As a result of this partial oxidation, several hydroxyl and carboxyl groups M and aldehyde groups and sugar groups are directed to the surface. The oxidation site has an anionic character, which means that in principle, any aqueous solution of anionic components that is intended to be applied to Myanmar is rejected. As a result, the coating film on the surface of the fiber is uneven and less effective. Therefore, the fiber has the disadvantages of being hydrophilic and not durable and deposited on the equipment during the carding process. The cationic silk finishing agent of the present invention (that is, in the aforementioned pH range) provides a positive contribution to the affinity of long fibers to the permanent hydrophilicity of the system. The bond between the long-twisted dimensional and square silk finishing agent's cationic components (see below for the decomposition of the surface of the kapf fiber / long fiber) is not a covalent bond, but it has ionic properties. This is not permanent, especially when the subsequent fiber water or This is especially true when water is in contact. However, according to the present invention, when the scale of the original paper between the surface of this fiber and the hydrophilic square silk finishing agent is applicable to the Chinese National Standard (CNS) Μ specification (210 X 297 gong) -13- (please read the precautions on the back first Fill in this page)

經濟部中央標準局員Η消費合作社印製 Α? Β7 五、發明説明(11 ) 鍵結*與纺絲整理劑成分之低溶解度/分散度組合時,其 效果足夠滿足親水性之「半永久性」之需求(亦即於一次 或多次施用後可再度溼潤性)。 坊絲整理劑之親水潤滑劑可維持於缳維表面上,因此 由於潤滑劑對水之親和性低及/或僅略可溶於水,故纖維 提供「半永久」親水性。特別令人感興趣者為親水成分, 由於其尺寸及/或構造僅微溶於水。 「潤滑劑」可Μ—般術語定義為控制摩擦力劑*亦即 可提高或降低摩擦力。有待控制的摩擦為纖維/缬維摩擦 (例如長纗維束之長纖維間之摩擦)或缠維/金屬摩擦( 例如長纖維與纖維生產設備之金屬部件間之摩擦)可於靜 態或動態條件下測量。此處所指摩擦係有閨缠維方向之摩 擦,纖維方向横向之摩擦(或摩擦力)稱為内聚力。當然 兩型摩擦接受纺絲整理劑影響。 當生產高速梳理作業用纖維時期望具有下列特性: 1. 需要高内聚力以便獲得合理的生產性質,例如由於_維 束更緊密故容易處理。也對填充於罐內程度產生影饔,其 又可獲得較大量批料因而獲得較高生產力。膨鬆的绦束( 由於纖维内聚力低)容易造成纖維非期望地堆積於辊上及 坊絲區段的“向日葵輪”上。 2. 期望中等(經控制的)織維/金屬摩擦,高度織維/金 靥摩擦適合某些目的,而低度纖維/金靥摩擦適合其他目 的。靜態缕維/金屬摩擦必須夠高Μ遴免長纗維於加工過 程中非期望的滑動。他方面*纖維/金靥摩擦遇高可能導 本纸張尺度逋用中國國家標準(CNS ) Α4规格(210 X 297公釐) -Μ ^ ^ 訂 气1 (請先閲讀背面之注意事項再填寫本頁) 經濟部中夬標準局負工消費合作杜印製 〇1^〇9S A7 — B7 五、發明説明(12) 致梳理上的問題,由於缴維難以從一根輥轉送到另一根輥 上。 3.高速梳理希望缠维/纖雄摩擦力髙,褥要高度摩擦力Μ 便將未黏合纖維網由椋理設備拉出進入黏合烘箱或軋機。 親水潤滑劑可適當選自烷氧化酵類、烷氧化酯類、烷 氧化釀胺類且可含小量親水改質(烷氧化)烴蠘。輯水潤 滑劑特別為通式I化合物 R1 X*Printed by the Consumer Standards Co., a member of the Central Bureau of Standards of the Ministry of Economic Affairs Α? Β7 V. Description of the invention (11) When the bond * is combined with the low solubility / dispersion of the spinning finish component, the effect is sufficient to meet the hydrophilic "semi-permanent" Demand (that is, rewetting after one or more applications). The hydrophilic lubricant of Fangsi finishing agent can be maintained on the surface of 缳 维. Therefore, since the lubricant has low affinity for water and / or is only slightly soluble in water, the fiber provides “semi-permanent” hydrophilicity. Of particular interest are hydrophilic ingredients, which are only slightly soluble in water due to their size and / or structure. "Lubricant" can be defined as a general term as a friction control agent * that can increase or decrease friction. The friction to be controlled is fiber / valve friction (such as the friction between long fibers of long bundles) or entanglement / metal friction (such as the friction between long fibers and metal parts of fiber production equipment). It can be in static or dynamic conditions. Next measurement. The friction here refers to the friction in the direction of the bodily dimension, and the friction (or friction) in the transverse direction of the fiber is called cohesion. Of course, the two types of friction are affected by the spinning finishing agent. The following characteristics are expected when producing fibers for high-speed carding operations: 1. High cohesion is required in order to obtain reasonable production properties, such as easy handling due to tighter bundles. It also affects the degree of filling in the tank, which in turn can obtain a larger amount of batch material and thus higher productivity. The bulky bunches (due to the low cohesion of the fibers) tend to cause undesirable accumulation of fibers on the rolls and the "sunflower wheel" in the Fangsi section. 2. It is expected that medium (controlled) weave / metal friction, high weave / golden friction will be suitable for some purposes, and low-fiber / golden friction will be suitable for other purposes. The static dimensional / metal friction must be high enough to prevent undesirable slippage during processing. Other aspects * The fiber / golden friction may be high. The paper standard may use the Chinese National Standard (CNS) Α4 specification (210 X 297 mm) -Μ ^ ^ Gas 1 (please read the precautions on the back before filling in This page) The Ministry of Economic Affairs, China National Standards Bureau, negative labor consumption cooperation du printing 〇1 ^ 〇9S A7 — B7 V. Description of the invention (12) Concerned about the carding problem, because the payment is difficult to transfer from one roller to another On the roll. 3. High-speed carding hopes that the dimensional / fibre friction friction is high, and the mattress needs a high friction force M to pull the unbonded fiber web from the finishing equipment into the bonding oven or rolling mill. The hydrophilic lubricant may be appropriately selected from alkoxylated yeasts, alkoxylated esters, alkoxylated amines and may contain a small amount of hydrophilic modified (alkoxylated) hydrocarbon worms. The water-based lubricant is a compound of formula I R1 X *

II

丄-Ζ2 I 其中 Z1 及 ZaSAlk-CONH-,(AU)a-N-,Allt-COO-,或H, 其中Aik為含至多24個碳原子之直鏈脂族烷基或烯基或多 於一個此等基之混合物,但Z1及ZaF可皆為H; R1為Η,CH3 ,含至多2 4個碳原子之烷基,或二亞甲基脂肪酸酯;R*為 Η或CH3; η為大於0之整數;B為大於0之整數;X-為相對雛 子。Aik特別為含6-14個碳原子,較佳8-12個碳原子之烷 基;η為1-4; ffl為1-10 ;及X-為乙酸,擰檬酸,乳酸,偏 硫酸或氯陰雛子。 欲調整纖維之摩擦特性,第二纺絲整理劑又可含有相 當小量,亦即不超過約1Q%重量比,典型地至多5%重量 比(K活性成分含量為準)熔點於4〇-12〇υ,典型40-90 它例如50-80Ό範圍之天然或合成烴蠟,或包括至少一種 烴蠟及具熔點於相同範園之蟣混合物。烴蠘特別為鏈烷烴 本紙張尺度適用中國國家揉準(CNS ) Α4規格(210 X 2.97公釐) -1 5 - __^ - ^一 訂 C* (,請先閲讀背面之注意事項再填寫本頁)丄 -Z2 I where Z1 and ZaSAlk-CONH-, (AU) aN-, Allt-COO-, or H, where Aik is a straight-chain aliphatic alkyl or alkenyl group containing up to 24 carbon atoms or more than one of these A mixture of equal groups, but Z1 and ZaF may both be H; R1 is Η, CH3, an alkyl group containing up to 24 carbon atoms, or a dimethylene fatty acid ester; R * is Η or CH3; η is greater than An integer of 0; B is an integer greater than 0; X- is a relative chick. Aik is especially an alkyl group containing 6-14 carbon atoms, preferably 8-12 carbon atoms; η is 1-4; ffl is 1-10; and X- is acetic acid, citric acid, lactic acid, partial sulfuric acid or Chlorine Yin child. To adjust the friction characteristics of the fiber, the second spinning finishing agent may contain a relatively small amount, that is, no more than about 1% by weight, typically at most 5% by weight (K active ingredient content prevails), melting point is 40- 12〇υ, typically 40-90 It is, for example, a natural or synthetic hydrocarbon wax in the range of 50-80 Ό, or it includes at least one hydrocarbon wax and a mixture with a melting point in the same range. Hydrocarbon worms are especially paraffins. The paper size is applicable to China National Standard (CNS) Α4 specifications (210 X 2.97 mm) -1 5-__ ^-^ One order C * (Please read the precautions on the back before filling in this page)

i、發明説明(13 ) 經濟部中央橾準局員工消費合作杜印製 蠘或微晶蠘,但也可使用天然蠼*亦即蟲蠘或植物孅。趟 也可含有某種量,亦即至多約4Q%簠量比之「烴樹脂J , 亦即具相對高熔點例如髙達約120C之部分交聯烴蠘。 蠟用於調節聚烯烴糸短纖維之摩擦特性*詳细討論於 PCT/DK95/00024 (併逑於此供於參考)。爾注意有瞄使用 此種蟣*雖然孅本性為疏水性,但K相當小量,例如如前 述不超遇5或10%摻混於本發明之坊絲整理劑,不會對孅 維之親水性產生不良的影響。 本發明使用之抗靜電劑係遵擇可獲得足夠抗靜電效果 ,同時大體不會干擾由親水潤滑劑提供的半永久的親水性 質。因為有效抗靜電劑經常為水溶性,故選擇正確的抗猙 電劑經常牽涉到一方面潤滑劑之期望的親水效果,與他方 面期望的抗睜電效果間之折衷問題。 第4銨化合物通常為良好抗靜電劑。此種產物進行乙 氧化反應可提高其水中溶解度,但因稀釋效果造成抗靜罨 效果較不顯著。水溶性或吸濕性化合物可促進抗靜電作用 ,但因此等化合物於系統溼潤時容易轉至液相,因而降低 效果之永久性,故必須小心選用化合物。處理此種工作之 一種方式係將負貴抗靜電作用之雄子基或極性基摻混於聚 合物材料内。 陽離子抗靜電劑可遘當選自胺類,豳胺類及烷氧化化 合物,特別烷氧化*例如乙氧化胺類及豳胺類。陽雛子抗 靜電劑特別為通式E化合物 本紙張尺度適用中國國家揉準(CNS ) A4洗格(210X2.97公釐) -16- I.--:------f -------—ΐτ------*-s— (請先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局員工消背合作社印裝 A7 __ B7 __ 五、發明説明(14 ) R1 X' R3-[〇~ (CH2) Jy-0- (CH2)a-[l^- (CH2) Jm-〇-[,:CH2):<-〇]z-R3 1工: i2 其中R1為H,CH3,含至多2 4個碳原子之烷基,或二亞甲基 脂肪酸酯;以為Η或CH3 ;各R3分別為Η,甲基*乙基或Aik -羰基,此處Aik為含至多24個碳原子之直鐽脂族烷基或烯 基或多於一基之混合物;B為大於0之整數;η為大於〇之整 數;X為2或3; y及ζ分別為大於Q之整數,y與ζ之總合至少 為5 ;及X-為相對離子。Alfc特別為含6-14個碳原子,較佳 8-12個碳原子之烷基;η為1-4;當R3為烷基時· R3為含6- 14個碳原子之烷基;Β為1-10;及X-為乙酸,檸檬酸,乳 酸,偏硫酸或氯陰離子。此型陽雛子抗靜電劑較佳具有分 子量至多約10 0 0,例如至多約6 〇 0。 本發明所用陽離抗靜電劑之共同特點為非剌激性化合 物。「非剌激性J一詞表示化合物於皮嫌剌激試驗或《晴 剌激試驗時歸類為非剌激性。可用方法有OECD指南4G4號 :「急性皮虜剌激/腐蝕」,1981年5月及OECD指南40 5 : 「急性眼睛剌激/腐蝕」,1987年2月,係於兔子進行。 分類可根據歐洲社區官方期刊L2 57,1 983所述分類。 纺絲整理分散液黏度受分散粒子或小滴大小影響。粒 子大小小,通常獲得低黏度,可於纖維表面上獲得纺絲整 理劑成分薄而均勻的分敗。此又提供具有均勻纖維/纖維 及纖維/金羼摩擦特性之缅維,可於捲曲機內獲得均匀變 * 形,随後於梳理過程中生產均勻的梳理網。最終结果為具 本紙張尺度適用中國國家標準(CNS ) A4规格(210X297公釐) 17 I---:丨'-----f I------1------、. C請先閏讀背面之注意事項再填寫本頁) 五、發明説明(15 Α7 Β7 經濟部中央橾準局員工消費合作社印製 有良好親水性之品質一致的非織材料。但要緊的是注意超 细粒子,例如直徑小於約Q.l jib粒子可能導致黏度增高。 因此纺絲整理分散液中粒子大小較佳於0.1-5 更佳於 0.1-2 jib之範圍。 一般而言*分散粒子之平均大小爾明顯小於缴維直徑 。對於直徑例如為15-20 μ®之典型细纖維而言,表示坊絲 整理分散液之粒子大小較佳至多約5 iU,更佳至多約2 ,最佳至多約1 。原則上平均粒子大小通常至少比纖維 直徑小一级,但依據兩種材料決定至某種程度。 分散粒子所需小粒子大小可Μ兩種方式逹成。第一方 式係使用相當大量乳化劑。但不希望纖維成品表面上含大 量乳化劑,如此會導致親水性之持久性喪失。第二種獲得 小粒子大小且為較佳方式係在分散液製備遇程中利用機械 方法,例如使用特殊均化裝置,高剪分散裝置或高速混合 機。 雖然希望將乳化劑數量維持於最小量,生成及維持分 散的極小粒子之安定分散液(典型的平均大小小於2 tfIB) 或含小滴之安定乳液之乳化劑用量通常需要Μ有限量使用 。因此,乳化劑之典型存在量低於1〇%重量比,更典型低 於8 %重置比,如4-7%重量比。理想上乳化劑數量需盡 可能小或甚至完全刪除。 適合用於本發明之坊絲整理劑之乳化劑為,例如脂肪 酸乙氧化物及例如通式I之脂肪酸乙氧化物 (.請先閲讀背面之注意事項再填寫本頁}i. Description of the invention (13) The bureau or microcrystalline burr produced by the consumer cooperation of the Central Department of Economics and Trade of the Ministry of Economic Affairs, but the natural burrard * that is, the worm or plant can also be used. The pass can also contain a certain amount, that is, up to about 4Q% of the "hydrocarbon resin J", that is, a partially cross-linked hydrocarbon worm with a relatively high melting point, such as about 120C. Wax is used to adjust polyolefin fiber The friction properties * are discussed in detail in PCT / DK95 / 00024 (and are here for reference). Please note that the use of this type of scorpion * Although the nature is hydrophobic, K is quite small, for example, as mentioned above In case of blending 5 or 10% of the square silk finishing agent of the present invention, it will not have an adverse effect on the hydrophilicity of the male dimension. The antistatic agent used in the present invention is compliant to obtain sufficient antistatic effect, while generally not Interfere with the semi-permanent hydrophilic properties provided by hydrophilic lubricants. Because effective antistatic agents are often water-soluble, choosing the right anti-calender agent often involves the desired hydrophilic effect of the lubricant on the one hand, and the anti-opening effect expected from the other side. The trade-off between electrical effects. The fourth ammonium compound is usually a good antistatic agent. The ethoxylation of this product can increase its solubility in water, but the antistatic effect caused by the dilution effect is less significant. Water solubility or hygroscopicity Change Substances can promote the antistatic effect, but when the system is wet, the compounds are easily transferred to the liquid phase, thus reducing the permanence of the effect, so the compound must be carefully selected. One way to deal with this work is to treat the expensive antistatic male The base or polar group is blended in the polymer material. The cationic antistatic agent can be selected from amines, vinylamines and alkoxylated compounds, especially alkoxylation * such as ethoxylated amines and vinylamines. Especially for the compound of general formula E, the paper scale is applicable to the Chinese National Standardization (CNS) A4 wash grid (210X2.97mm) -16- I .--: ------ f --------- Ιτ ------ *-s— (please read the precautions on the back before filling in this page) Printed by the Employees ’Cooperative Society of the Central Standards Bureau of the Ministry of Economic Affairs A7 __ B7 __ 5. Description of the invention (14) R1 X’ R3 -[〇 ~ (CH2) Jy-0- (CH2) a- [l ^-(CH2) Jm-〇- [,: CH2): < -〇] z-R3 1 work: i2 where R1 is H, CH3, an alkyl group containing up to 24 carbon atoms, or a dimethylene fatty acid ester; to be Η or CH3; each R3 is Η, methyl * ethyl or Aik-carbonyl, where Aik contains up to 24 Straight carbon atoms Aliphatic alkyl or alkenyl or a mixture of more than one group; B is an integer greater than 0; η is an integer greater than 0; X is 2 or 3; y and ζ are integers greater than Q, respectively, the total of y and ζ The sum is at least 5; and X- is a relative ion. Alfc is especially an alkyl group containing 6-14 carbon atoms, preferably 8-12 carbon atoms; η is 1-4; when R3 is an alkyl group · R3 is An alkyl group containing 6 to 14 carbon atoms; B is 1-10; and X- is acetic acid, citric acid, lactic acid, partial sulfuric acid, or chloride anion. This type of anti-static agent for larvae preferably has a molecular weight of at most about 100 , For example, at most about 6.00. The common feature of the cationic antistatic agent used in the present invention is a non-stimulating compound. "The term" non-stimulatory J "indicates that the compound is classified as non-stimulatory in the skin irritant test or the" clear stimulus test. Available methods are OECD Guideline 4G4: "Acute skin stimulus / corrosion", 1981 May 2015 and OECD Guide 40 5: "Acute eye irritation / corrosion", February 1987, carried out in rabbits. The classification can be based on the description in the European Community Official Journal L2 57, 1 983. The viscosity of the spinning finishing dispersion is affected by the size of the dispersed particles or droplets. The particles are small in size and usually have a low viscosity, and a thin and uniform spin finish composition can be obtained on the fiber surface. This in turn provides Burmese with uniform fiber / fiber and fiber / gold friction characteristics, which can be uniformly deformed in the crimping machine, and then produce a uniform carding net during the carding process. The final result is that the Chinese paper standard (CNS) A4 specification (210X297 mm) is applied to the paper size. 17 I ---: 丨 '----- f I ------ 1 ------ 、 C Please read the notes on the back before filling in this page) 5. Description of the invention (15 Α7 Β7 The Ministry of Economic Affairs, Central Bureau of Accreditation and Employee Consumer Cooperatives printed a non-woven material with good hydrophilicity and consistent quality. But what matters is Note that ultra-fine particles, such as particles with a diameter less than about Ql jib, may cause an increase in viscosity. Therefore, the particle size in the spinning finishing dispersion is preferably in the range of 0.1-5 and more preferably in the range of 0.1-2 jib. In general * average of dispersed particles The size is significantly smaller than the pay-off diameter. For typical fine fibers with a diameter of, for example, 15-20 μ®, the particle size of the Fangsi finishing dispersion is preferably at most about 5 iU, more preferably at most about 2, and most preferably at most about 1. In principle, the average particle size is usually at least one level smaller than the fiber diameter, but it is determined to a certain extent according to the two materials. The small particle size required to disperse the particles can be achieved in two ways. The first way is to use a considerable amount of emulsification Agent, but it is not Emulsifier, which will lead to the permanent loss of hydrophilicity. The second way to obtain small particle size and is the best way is to use mechanical methods in the preparation of dispersions, such as the use of special homogenization equipment, high shear dispersion equipment or high speed Mixer. Although it is desirable to keep the amount of emulsifier to a minimum, a stable dispersion of very small particles (typical average size less than 2 tfIB) to generate and maintain dispersion or the amount of emulsifier with a stable emulsion containing droplets usually requires a limited amount of M Use. Therefore, the typical amount of emulsifier present is less than 10% by weight, more typically less than 8% reset ratio, such as 4-7% by weight. Ideally the amount of emulsifier needs to be as small as possible or even completely deleted. Suitable emulsifiers for the square silk finishing agent of the present invention are, for example, fatty acid ethoxylates and fatty acid ethoxylates such as general formula I (please read the precautions on the back before filling this page)

本紙張尺度適用中國國家標準(CNS ) Α4規格(210X297公4 ) 18 經濟部中央橾準局員工消費合作社印策 A7 _B7_ 五、發明説明(l6 ) Θ-Χ-(O^-CH-OVHi ill 丨 i2 i ( 此處R1為含8-100個碳原子較佳10-80碳原子之直鐽或分支 烷基或烯基,X為NH,0,S,COO或C0,以為!!,Cfl3或含至 多4個碳原子之综基,及ffl為3-100,較佳5-60。 如前解釋,纺絲整理劑之黏度較佳盡可能低。特別第 二纺綠整理劑黏度較佳至多7 BPas,更佳至多5 mPas, 又更佳至多3 ePas,最佳至多2 fflPas,例如使用光學試 管型黏度計於23C及2.Q sec·1剪率測量。 要緊地使用坊絲整理劑(圼分散液或於水之乳液,水 作為連鱭相)後,纺織整理劑之活性化合物可分散至纖維 表面曆。可於捲曲前、中或後,將經坊綠整理劑塗覆之長 缠維置於(高於坊絲整理劑分散液主要活性成分熔點之) 溫度下進行,亦即如前所述。 消泡劑典型地於第二坊絲整理劑中加至抗靜镫劑。消 泡劑例如為聚矽氧化合物,例如二甲基矽氧烷或聚二甲基 矽氧烷,例如親水改質聚二甲基矽氧烷,典型添加量基於 纺絲整理劑之活性成分含惫,例如1 %重量比,典型低於 0.5%重量比,例如約0.25%重量比。但此種矽化合物於 某些例中可以略為大量添加,亦即高達约5%重量比,但 通常Μ低於1 %重量比之量為佳。第一坊絲整理劑較佳不 含聚矽氧化合物。其他非聚矽氧系消泡劑也可使用。 除第一坊絲整理劑包括至少一種親水潤滑劑外,也可 包括至少一種第二坊絲整理劑所含該型陽雛子抗靜電劑。 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐) 19 I---,------Ο ! (.請先閲请背面之注意事項再填窝本頁) 訂 經濟部中央標準局員工消费合作社印製 313595 A7 B7 五、發明説明(17 ) . 同理,第二纺絲整理劑可含至少一種第一坊絲整理劑所含 該型親水潤滑劑,若有所需*可使用相同坊絲整理劑作為 第一及第二纺絲整理劑。第一及/或第二纺綠整理劑之活 性成分含量較佳包括至少50%,典型至少65%—種或多種 潤滑劑及至多5 0%,典型至多35% —種或多種抗靜電劑及 /或乳化劑。 坊絲整理劑内活性成分(亦即抗靜電劑、潤滑劑、乳 化劑)總濃度,典型約1-1Q%重量比,在此範圍低端之量 常用於第一纺絲整理劑,而在中端及高端之量常用於第二 纺絲整理劑,導致纖維具有乾燥後坊絲整理劑塗膜,典型 約占缴維之約0. 2-0.5%重量比。 繼雒表而之分解 根據本發明希望獲得孅維表面在缳維生產遇程中略為 分解。「分解」一詞於本文表示纖維表面之聚合物鐽進行 經控制的分解,獲得陰離子表面基團,陰離子基團可與坊 絲整理劑之陽離子成分生成離子鍵,因此有助於將坊絲整 整劑維持於纖維表面。長纖維表面之分解係在聚合物送出 棋具而暴露於空氣時進行,空氣中的氧與聚合物反懕至某 種程度時聚合物分解。分解特別包括鏈剪掉且在某些位置 碳氧化,結果含碳化學基如=C0, -CH0及-C00H可在钃維表 面测得,此等基具有陰離子性質,因此容易被用來處理纗 維的纺絲整理劑内之陽離子基吸引。 必須考慮多種因素K便遴成纖維表面所需分解。第一 因素為纺絲過程必須於顯然高於聚合物熔點之溫度進行。 本紙張又度適用中國國家標準(CNS ) A4規格(210X 297公釐) -2 0 - (.請先閲讀背面之注意事項再填寫本頁)This paper scale is applicable to the Chinese National Standard (CNS) Α4 specification (210X297 gong 4) 18 Printed by the Central Consumer ’s Bureau of the Ministry of Economic Affairs Employee Consumer Cooperative A7 _B7_ V. Description of the invention (l6) Θ-Χ- (O ^ -CH-OVHi ill丨 i2 i (where R1 is a straight or branched alkyl or alkenyl group containing 8-100 carbon atoms, preferably 10-80 carbon atoms, X is NH, 0, S, COO or C0, think !, Cfl3 Or a comprehensive group containing up to 4 carbon atoms, and ffl is 3-100, preferably 5-60. As explained before, the viscosity of the spinning finishing agent is preferably as low as possible. Especially the viscosity of the second spinning green finishing agent is better Up to 7 BPas, better up to 5 mPas, better up to 3 ePas, and best up to 2 fflPas, for example, using an optical test tube type viscometer to measure at 23C and 2.Q sec · 1 shear rate. Use square wire finishing agent urgently (Simultaneous dispersion or emulsion in water, water as the cocoon phase), the active compound of the textile finishing agent can be dispersed to the surface of the fiber. It can be coated with Jingfang green finishing agent before, during or after curling. The entanglement is carried out at a temperature (higher than the melting point of the main active ingredient of Fangsi finishing agent dispersion liquid), that is, as described above. It is added to the anti-static stirrup agent in the second square silk finishing agent. The defoaming agent is, for example, polysiloxane, such as dimethylsiloxane or polydimethylsiloxane, such as hydrophilic modified polydimethylsiloxane The typical addition amount is based on the active ingredient of the spinning finishing agent, such as 1% by weight, typically less than 0.5% by weight, such as about 0.25% by weight. However, such silicon compounds are used in some cases It can be added in a large amount, that is, up to about 5% by weight, but usually the amount of M is less than 1% by weight. The first square silk finishing agent is preferably free of polysiloxane compounds. Other non-polysiloxane-based consumers Foaming agents can also be used. In addition to the first square silk finishing agent including at least one hydrophilic lubricant, it can also include at least one type of Yangfangzi antistatic agent contained in the second square silk finishing agent. CNS) Α4 specification (210X297mm) 19 I ---, ------ Ο! (Please read the precautions on the back before filling the nest page) Printed by the employee consumer cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs 313595 A7 B7 V. Description of the invention (17). Similarly, the second spinning finishing agent may contain at least This type of first square silk finishing agent contains this type of hydrophilic lubricant. If necessary, the same square silk finishing agent can be used as the first and second spinning finishing agents. The first and / or second spinning green finishing agent The content of active ingredients preferably includes at least 50%, typically at least 65%-one or more lubricants and at most 50%, typically at most 35%-one or more antistatic agents and / or emulsifiers. (That is, antistatic agent, lubricant, emulsifier) The total concentration is typically about 1-1Q% by weight. In this range, the low-end amount is often used in the first spinning finishing agent, and the middle-end and high-end amount is commonly used. 2-0.5% 重量 比。 In the second spinning finishing agent, resulting in fibers with a dried square silk finishing agent coating film, typically accounted for about 0. 2-0.5% by weight of the payment. According to the present invention, it is expected that the surface obtained by the method may be slightly decomposed during the process of production. The term "decomposition" means that the polymer on the surface of the fiber undergoes a controlled decomposition to obtain anionic surface groups, which can form ionic bonds with the cationic component of Fangsi finishing agent, thus helping to organize Fangsi The agent is maintained on the fiber surface. The decomposition of the surface of the long fiber is carried out when the polymer is sent out of the chess set and exposed to air. When the oxygen in the air reacts with the polymer to a certain extent, the polymer decomposes. Decomposition especially includes chain scission and carbon oxidation at certain positions. As a result, carbon-containing chemical groups such as = C0, -CH0 and -C00H can be measured on the surface of the dimensional metal. These groups have anionic properties, so they are easily used to treat The cationic group in the spinning finishing agent of Victoria is attracted. Various factors K must be considered to select the desired decomposition of the fiber surface. The first factor is that the spinning process must be carried out at a temperature clearly above the melting point of the polymer. This paper is again applicable to the Chinese National Standard (CNS) A4 specification (210X 297mm) -2 0-(. Please read the precautions on the back before filling this page)

、1T 經濟部中央樣準局負工消費合作杜印製 A7 B7 ______ 五、發明説明(18 ) 因此纺綠溫度至少比聚合物熔點高9GI,更佳至少高100 它,典型至少高110¾。另一因素為坊絲箧内之淬冷空氣 流。如此淬冷空氣流速高,更快速冷卻纖維,结果獲得低 度纖維表面分解而使用較低的空氣流速時可獲得較高度分 解作用。高度分解(利用淬泠空氣速度低獲得)及對部分 分解纖維表面具有高度親和力之親水纺絲整理劑,可導致 缬維具有改良的永久性親水性,同理,由纖維生產的非纖 物也具有相同性質。然而纖維表面分解程度必須不夠高, 歸因於分解過高導致非織物之強度降低,但此種纖維及非 織物之親水性之持久性良好。 原則上*纖維表面分解程度裨單獮於表層測定,由於 此種分解相信為僅影響纖维外表的現象,而纖維中部相信 大體不受分解過程影響。然而,實際上目前並無單獨測定 纖維表面分解程度之方法。下文所陳纖維表面分解實際上 為分析整個潘維後之估值。如此鑲維表面分解程度可定量 為纺絲缬維之MFI (熔體流指數)與聚合物原料之MFI比較 之關係,MFI係根據ISO 1133-81(E)測定。聚丙烯纖維之 MFI(|S)i / MFI(粗材科):比,例如於約2.4-3.0之範圍。 含本發明之缬維之梳理網黏合而生產非織物可藉已知 手段進行,例如使用軋櫬或熱空氣烘箱作熱黏合,超音波 黏合或紅外線加熱。 宙昼非继物:>半余众件丹親太袢誓夕方法 下逑試驗除非另行指示,否則係基於使用非織物樣品 ,根據ISO 90 73.1 : 1989 (質最/單位面積之测定)测得 本紙張尺度逋用中國國家標準(CNS ) A4规格(210X 297公嫠) -21 - ----------^ ^ — — (. 請先聞讀背面之注意事項再填寫本頁), 1T Ministry of Economic Affairs, Central Bureau of Prototyping and Duty Printing Cooperative Printing A7 B7 ______ V. Invention Description (18) Therefore, the spinning temperature is at least 9GI higher than the melting point of the polymer, preferably at least 100 higher, typically at least 110¾ higher. Another factor is the quenching air flow in Fang Sihao. In this way, the quenching air flow rate is high, and the fiber is cooled more quickly. As a result, a low degree of fiber surface decomposition is obtained and a higher degree of decomposition can be obtained when a lower air flow rate is used. Highly decomposable (obtained by low quenching air speed) and a hydrophilic spinning finish with a high affinity for the surface of partially decomposed fibers, which can lead to improved permanent hydrophilicity of Valerian. Similarly, non-fibrous materials produced from fibers Have the same nature. However, the degree of decomposition of the fiber surface must not be high enough, because too high decomposition results in a decrease in the strength of the non-woven fabric, but the hydrophilicity of such fibers and non-woven fabrics has good durability. In principle, the degree of decomposition of the fiber surface is easy to measure in the surface layer, because this decomposition is believed to be a phenomenon that only affects the appearance of the fiber, and the middle of the fiber is believed to be largely unaffected by the decomposition process. However, in practice, there is currently no separate method for determining the degree of fiber surface decomposition. The decomposition of the surface of the aged fiber described below is actually an estimate after analyzing the entire Pan Wei. In this way, the degree of surface decomposition of the mounting dimension can be quantified as the relationship between the MFI (melt flow index) of the spinning valvi and the MFI of the polymer raw material. The MFI is measured according to ISO 1133-81 (E). Polypropylene fiber MFI (| S) i / MFI (rough materials): ratio, for example, in the range of about 2.4-3.0. The production of non-woven fabrics by bonding the carded web containing the valvi of the present invention can be carried out by known means, for example, by rolling or hot air oven for thermal bonding, ultrasonic bonding or infrared heating. Zhou Dayu is not a successor: > more than half of the pieces of the Dan pro-Taiwan oath method under the test unless otherwise instructed, is based on the use of non-fabric samples, according to ISO 90 73.1: 1989 (measurement of quality / unit area) The size of the paper used is in accordance with the Chinese National Standard (CNS) A4 (210X 297). -21----------- ^ ^ — — (. Please read the precautions on the back before filling in this page)

、1T 五、發明説明(19 ) A7 B7 基重為20 g/ ma。 3次盤窀方法 此乃基於ED ANA標準ERT 150 . 2-9 3號之修改ED ANA方法 。有關標準方法之修改部分為對非織物上精確同一點進行 3次擊穿測量,每次擊穿回合後替換下方吸收點(滤紙) 。各回合間非織物未經乾燥或K任何方式拭除。進行三序 列(每序列各三回合),計算各回合之測量值之平均值及 標準偏差。試驗中三回合擊穿時間至多2D秒,較佳至多10 秒,更佳至多5秒。 3 X 1 0孔方法 兩張滹紙彼此重叠,光滑面向上,非織物樣品放置於 滹紙中心頂上。然後10孔不锈鋼板( 2 2 0 X 50 X 5 ana,孔直 徑15 mm)放置於非继物頂上。一滴合成尿液(〇.9%NaCl 溶液)置於10孔各別之非織物上,若該滴在2秒内被非織 物吸收則給一分。60秒後如同第一回合再放置10滴,2秒 内被吸收則再給一分。60秒後相同方式進行第三回合,故 所得總分為3D。若分數和大於27則稱非織物為「半永久性 經濟部中央標準局—工消費合作社印製 液體趿牧試驗 另一種测定非織物之親水性之適當方法係根據ED AN A 對非镟物吸收之推萬試驗(No. 10.1-72)進行液體吸收時 間試驗。本試驗包括測董長條樣品(5g)鬆鬆捲入筒形網籃 (3g)内且從25m高度下落至液體(典型為水)表面其完全 溼潤所需時間。此試驗用之非纖物樣品供本發明之用,至 (請先閲讀背面之注意事項再填寫本頁), 1T V. Description of the invention (19) A7 B7 basis weight is 20 g / ma. The 3rd rounding method This is a modified ED ANA method based on ED ANA Standard ERT 150. 2-9 No. 3. The modified part of the standard method is to perform three breakdown measurements on the exact same point on the non-woven fabric, and replace the lower absorption point (filter paper) after each breakdown round. The non-woven fabrics in each round were not wiped off by drying or K in any way. Perform three series (three rounds for each series) to calculate the average and standard deviation of the measured values for each round. The breakdown time of the three rounds in the test is at most 2D seconds, preferably at most 10 seconds, more preferably at most 5 seconds. 3 X 1 0 hole method Two papers overlap each other with the smooth side facing upwards, and the non-woven sample is placed on top of the center of the paper. Then a 10-hole stainless steel plate (2 2 0 X 50 X 5 ana, hole diameter 15 mm) is placed on top of the non-secondary. A drop of synthetic urine (0.9% NaCl solution) is placed on 10 holes of each non-woven fabric. If the drop is absorbed by the non-woven fabric within 2 seconds, a point will be given. After 60 seconds, place another 10 drops as in the first round. If absorbed within 2 seconds, give another point. After 60 seconds, the third round is performed in the same manner, so the total score is 3D. If the score is greater than 27, the non-woven fabric is called "Semi-permanent Central Bureau of Standards-Ministry of Economic Affairs-Industry and Consumer Cooperatives Printed Liquid Fangmu Test. Another suitable method for determining the hydrophilicity of non-woven fabrics is the absorption of non-woven materials according to ED AN Push the Wan test (No. 10.1-72) to conduct the liquid absorption time test. This test includes measuring the long strip sample (5g) loosely rolled into the cylindrical mesh basket (3g) and falling from a height of 25m to the liquid (typically water) ) The time it takes for the surface to fully wet. The non-fibrous sample used in this test is for the purpose of this invention, to (please read the precautions on the back before filling this page)

本紙張尺度適用中國國家標準(CNS ) A4规格(210X 297公釐) 22 經濟部中央標準局員工消费合作社印製 A7 _B7 五、發明説明(20 ) 少於23¾及5D%相對溼度調理2小時。 前述液體吸收試驗也可作某些小量修改用Μ测定鑛維 之親水性。欲测定纖維之親水性,將有待試驗纖維於15 Β /Bin梳理,製備具有基重約1〇 g/m«之梳理網,然後由 梳理網取得5 g重最樣品。其餘試驗係根據ED AN A試驗程序 (10.1-72)進行。試用非镰物或織維時,吸收時間定義為 容納非織物或纖維樣品之網籃撞擊液面刹那至樣品完全浸 沒於液面下方剎那經歷的時間間隔。 前述水中液體吸收性試驗中,非織物或親水纖雄樣品 之溼潤時間需至多一分鐘,典型至多30秒,較佳至多2 0秒 更佳至多10秒,最佳至多5秒。 再度溼潤試驗 非織物之再度溼潤係根據EDANA摞準方法第ERT 151.0 -93號測定。結果Mg表示為三次個別測量之平均。本試驗 測定非織物作為液髖從幾近飽和吸收材料運送至乾堍吸收 材料之障壁能力。非缃物下方之吸收材料為85炻液體胞和 度》颳縮3分鐘後濉紙塊置於非織物頂上,砝碼置於滅紙 頂上。2分鐘後移開砝碼,記錄瀘紙的增重。試驗中再度 溼潤,亦即濾紙之增重較佳至多G.3g,更佳至多(L2g,最 佳至多〇 . lg。 抗拉強麻 抗拉強度係根據EDANA 7Q.2-89於機器方向(MD)及横 向(CD)測定。黏合指數(BI)係於不同黏合溫度計算,黏合 指數定義為機器方向強度與横向強度之乘積之平方根。對 本紙張尺度適用中國國家標隼(CNS ) A4規格(210X 297公釐) -23- ^ fIT41 (請先閲讀背面之注意事項再填寫本頁) 經濟部中央揉準局貝工消費合作社印装 A7 B7 五'、發明説明(21 ) 標準非缴物基S20 g/®s達到標準黏合指數,特定 樣品的黏合指數計算值乘以20除K真正基重(g/aa),因 而補償非織物強度陳基重改變之事實。表示於黏合 溫度範圍之黏合指數最大值。 奮例 纖維及非織物係如下述製備: 聚烯烴原料(等規聚丙烯)利用習知坊絲(長坊)技 術,使用纺絲速度2GQQ B/ain坊成纖雄,獲得數百根長 纖維束。長纖維利用空氣冷卻淬冷後,利用剌輥Μ第一访 絲整理劑處理*接著使用熱輥與熱空氣烘箱之姐合以二階 段式抽拉操作離線拉伸*溫度係於115-13 5t:之範圍。拉 伸比約為1.25:1。然後拉伸後的長激維(利用剌輥)Κ第 二纺絲整理劑處理,於此等實例中,第二纺絲整理劑係與 第一纺絲整理劑相同。然後長纖維於填塞箱捲曲機内捲曲 ,陳後於約1251C溫度之烘箱内退火俾減少熱黏合過程中 纖維收縮且使纺絲整理劑的親水成分均勻分布於纖維表面 。然後將長缴維切成所霈長度而生產短缴維。纖維之细度 為 22 dtex, 纖維之丹尼數為1.8-2.1 cN/dtex,斷裂點 伸度為350-420%,約10-13捲/ca,及切割長度為41或45 am。經整理纖維细度根據DIN 5 381 2/2測量,缴維之斷裂 點伸度及丹尼數係根據DIN 53816測量,而捲曲頻度係根 據 ASTM D 3937-82測量。 非继物係由多種纖維經由於100 m/Bin椋理及於161 C熱黏合(滾軋黏合)纖維網製備非继物。各非織物及抗 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) -2 4 - (.請先閱讀背面之注意事項再填寫本頁)This paper scale is applicable to the Chinese National Standard (CNS) A4 specification (210X 297 mm) 22 Printed by the Employee Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs A7 _B7 V. Description of the invention (20) Less than 23¾ and 5D% relative humidity conditioning for 2 hours. The aforementioned liquid absorption test can also be modified with certain small amounts to determine the hydrophilicity of mineral dimension with M. To determine the hydrophilicity of the fiber, the fiber to be tested was carded at 15 Β / Bin to prepare a carded web with a basis weight of about 10 g / m, and then the carded web was used to obtain a sample with a weight of 5 g. The rest of the tests were conducted according to the ED AN A test procedure (10.1-72). When using non-sickle or weave dimensions, the absorption time is defined as the time interval between the moment when the basket containing the non-woven or fiber sample hits the liquid surface and the sample is completely submerged under the liquid surface. In the aforementioned liquid absorption test in water, the wetting time of the non-woven or hydrophilic fiber sample needs to be at most one minute, typically at most 30 seconds, preferably at most 20 seconds, more preferably at most 10 seconds, and most preferably at most 5 seconds. Rewetting test The rewetting of non-woven fabrics is measured according to the EDANA stacking method No. ERT 151.0-93. The result Mg is expressed as the average of three individual measurements. This test measures the barrier capacity of non-woven fabrics as a liquid hip to be transported from near-saturated absorbent materials to dry pad absorbent materials. The absorbent material under the non-contained object is 85 stoneware liquid cells. After scraping for 3 minutes, the paper block is placed on the top of the non-woven fabric, and the weight is placed on the top of the paper extinction. Remove the weight after 2 minutes and record the weight gain of the paper. Wet again in the test, that is, the weight gain of the filter paper is preferably at most G.3g, more preferably at most (L2g, best at most.lg. Tensile strength hemp Tensile strength is based on EDANA 7Q.2-89 in the machine direction ( MD) and transverse (CD) measurement. The adhesion index (BI) is calculated at different adhesion temperatures. The adhesion index is defined as the square root of the product of the machine direction strength and the transverse strength. For this paper scale, the China National Standard Falcon (CNS) A4 specification is applied ( 210X 297 mm) -23- ^ fIT41 (please read the notes on the back before filling in this page) Printed A7 B7 Five ', Invention Description (21) Standard Non-Contributable Base of the Ministry of Economic Affairs, Central Bureau of Economic Cooperation and Development, Beigong Consumer Cooperatives S20 g / ®s reaches the standard adhesion index. The calculated value of the adhesion index of a specific sample is multiplied by 20 divided by the K real basis weight (g / aa), thus compensating for the fact that the non-fabric strength and basis weight change. It is expressed in the bonding temperature range of adhesion The maximum value of the index. The fiber and non-woven fabrics of the example are prepared as follows: Polyolefin raw materials (isotactic polypropylene) use the conventional square wire (long square) technology, using a spinning speed of 2GQQ B / ain square to form a fiber male, and obtain the number of Hundreds of long fiber bundles. After the fiber is quenched with air cooling, it is treated with the squeegee M first silk finishing agent. * Then using a hot roller and hot air oven sister to perform a two-stage drawing operation offline drawing * The temperature is 115-13 5t: The drawing ratio is about 1.25: 1. Then, after the stretching, the long-shock dimension (using the roll) K is treated by the second spinning finishing agent. In these examples, the second spinning finishing agent is the same as the first The spinning finishing agent is the same. Then the long fiber is curled in the stuffing box crimping machine, and then annealed in an oven at a temperature of about 1251C to reduce fiber shrinkage during thermal bonding and make the hydrophilic component of the spinning finishing agent evenly distributed on the fiber surface. Cut the long-duration to the length of the centipede to produce the short-duration. The fineness of the fiber is 22 dtex, the fiber Danny number is 1.8-2.1 cN / dtex, and the elongation at break is 350-420%, about 10-13 Coil / ca, and the cutting length is 41 or 45 am. The fineness of the finished fiber is measured according to DIN 5 381 2/2, the extension of the breaking point of the pay-off and the Danny number are measured according to DIN 53816, and the crimp frequency is according to ASTM D 3937-82 measurement. Non-secondary system consists of multiple fibers through 100 m / Bin And prepare non-secondary materials on 161 C heat-bonded (rolled-bonded) fiber web. For each non-woven fabric and paper-resistant paper, the Chinese National Standard (CNS) A4 specification (210 X 297 mm) -2 4-(.Please first (Read the notes on the back and fill in this page)

A 313535 A7 B7 經濟部中央標準局負工消費合作社印裝 五、發明説明(22 ) 拉強度及伸度係於櫬器方向及横向(定義如上)(亦即使 用EDANA推駑試驗)測量,黏合性指數係如前述基於抗拉 強度测量值求出。此外也測定擊穿,再度溼潤及撥水性等 性質*所用方法也如前述。 椋理性,亦即镰维對梳理的適合性係使用簡軍潘維網 内聚力試驗澜定。試驗方式係測量約10 之稀薄梳理 纖維網可支撐於大體水平位置不會由於本身重量而斷裂之 長度,梳理網長度以約15 b/min之速率壻加。進行方式 係將梳理網由椋理機中於水平方向K 15 a/min速度去除 ,此速度乃本試驗所用梳理速度。 潘維/鑛維摩擦力愈高則梳理性愈髙,獲得更高的缬 維網内聚力長度。纘維/纖維摩擦力與多種因素有關,例 如第二纺絲整理劑組成及變形程度Μ及變形之永久性如何 。纖維/金靥摩擦力對梳理也重要;若過高或遇低則纖維 難以蓮送通過梳理櫬。 極為適合梳理之聚烯烴纖維典型地可於前述潘維網内 聚長度試驗中,支撐約1.5皿或Κ上,例如1.5-2.5 m。設 計供高速梳理之纖維較佳可支撐略長,亦即至少約2.0 a 〇 下表顯示第一、第二及第三擊穿值(秒),再度溼潤( 克),孅維上纺絲整理劑數量(占纖維之%重量比)缬維 網内聚力(米),機器方向及横向之抗拉強度(N/5 ca〇, 及黏合性指數最大值,全部皆如上說明測定。有蘭各例之 附註提供於表後。 (請先閲讀背面之注意事項再填寫本頁) 訂 A ... 本紙張尺度適用中國國家橾準(CNS ) A4規格(210X 297公釐) -2 5 - 〇lS595 A7 __B7五、發明説明(23 ) 1- 2* 3.1* 3.2* 3½ ®»4J 苕涵社一 苕囫#1 苕囫#1 S截屮 蟊雞屮 sjt 屮 S雞屮A 313535 A7 B7 Printed by the Consumer Labor Cooperative of the Central Bureau of Standards of the Ministry of Economy V. Description of invention (22) Tensile strength and elongation are measured in the direction and transverse direction of the frame (as defined above) (that is, using the EDANA push test), and bonded The sex index is calculated based on the tensile strength measurement value as described above. In addition, the properties of breakdown, rewetting and water repellency * were also measured * using the same method as described above. The rationality, that is, the suitability of Siwei for carding, is determined by the use of Jianjun Panwei Net Cohesion Test. The test method is to measure the length of a thin carded web of about 10 that can be supported at a substantially horizontal position without breaking due to its own weight. The length of the carded web is increased at a rate of about 15 b / min. The way of proceeding is to remove the carding net from the horizontal machine at a K 15 a / min speed in the horizontal direction. This speed is the carding speed used in this test. The higher the friction between Panwei and Mine, the higher the combability, and the higher the cohesion length of the Valvi net. The dimensional / fiber friction is related to many factors, such as the composition of the second spinning finishing agent and the degree of deformation M and the permanence of the deformation. The fiber / golden friction is also important for carding; if it is too high or low, the fiber is difficult to pass through the card. Polyolefin fibers that are very suitable for carding are typically supported in the aforementioned Panway mesh cohesion length test, supporting about 1.5 dishes or K, for example 1.5-2.5 m. Fibers designed for high-speed carding preferably support slightly longer, that is, at least about 2.0 a. The following table shows the first, second, and third breakdown values (seconds), re-wetting (grams), and spin-up finishing The amount of the agent (% by weight of the fiber), the cohesive force of the valve mesh (m), the tensile strength in the machine direction and the transverse direction (N / 5 ca〇, and the maximum value of the adhesion index are all determined as described above. There are blue cases The notes are provided after the table. (Please read the precautions on the back before filling in this page) Order A ... This paper size is applicable to China National Standard (CNS) A4 specification (210X 297mm) -2 5-〇lS595 A7 __B7 V. Description of the invention (23) 1- 2 * 3.1 * 3.2 * 3½ ® »4J 苕 涵 社 一 苕 囫 # 1 苕 囫 # 1 S 切 屮 蟊 鸡 屮 sjt 屮 S 鸡 屮

Eo-»»a®« Μ»φ_ -81 3.99 ϊοο 09 5.67 14.64 -22 产2'coFs 94 2.40 3.23 -6 Ϊcni—» ,2 3.3 4.8 2.7 4.8 12.3 0」 2.S^03产05C5b 0 1 雲 1 to2 6 3 9 0.26 07 13 15 lco 0.45 45 30 35 办5 s .20 .50 馘, 挪111 «渐藤鐘 (請先閱讀背面之注意事項再填寫本頁) *·1Τ 經濟部中央標準局員工消費合作杜印製 2.25 -00 -75 .25 .75 ,25 -75 1.75 1.75 3Co ,6 9 -7 11 13 -7 6 29·9 Ξ 34·4 11.3 33 35 31 35 42 17 36 鷀籂1S3«Λ 2 3 9.7 16.1 17.86 17.4 16.5 19.1 23 10 Η 19 本紙張尺度適用中國國家標準(CNS ) Α4規格(2ίΟΧ297公釐) 26Eo-»» a® «Μ» φ_ -81 3.99 ϊοο 09 5.67 14.64 -22 production 2'coFs 94 2.40 3.23 -6 Ϊcni— », 2 3.3 4.8 2.7 4.8 12.3 0 ″ 2.S ^ 03 production 05C5b 0 1 cloud 1 to2 6 3 9 0.26 07 13 15 lco 0.45 45 30 35 Office 5 s .20 .50 馘 , Norwegian 111 «Kanato Clock (Please read the notes on the back before filling this page) * · 1ΤMinistry of Economic Affairs Central Standards Bureau Employee consumption cooperation Du Printing 2.25 -00 -75 .25 .75, 25 -75 1.75 1.75 3Co, 6 9 -7 11 13 -7 6 29 · 9 Ξ 34 · 4 11.3 33 35 31 35 42 17 36 鹚 籂 1S3 «Λ 2 3 9.7 16.1 17.86 17.4 16.5 19.1 23 10 Η 19 This paper scale is applicable to China National Standard (CNS) Α4 specification (2ίΟΧ297 mm) 26

MD CD BL· 經濟部中央標準局員工消費合作社印製 A7 B7五、發明説明(24 ) 實例之附註 實例1 (比較例)使用典型改質(乙氧化)聚矽氧坊 絲整理劑,纖維具有相對低丹尼數及中度再度溼潤性。系 統之持久性相當良好。纺綠整理劑含約3(3%改質聚矽氧, 抗靜電劑大半為乙氧化脂肪酸鹽。 實例2 (比較例)使用於實例1之相同抗靜電成分, 但聚矽氧由醅類介面活性劑替代。持久性及丹后數不夠好 ,但纖維性質尚稱滿意。 實例3.1,3. 2及3.3 (比較例)顯示經由提高聚合物 熔體溫度(分別為295¾,3 0 0 ¾及3 0 5 ¾)同時冷卻空氣 及其他條件保持恆定,所得纖維表面之分解。可藉施於灌 維之坊絳整理劑數量隨纖維表面分解作用增加而增加。可 能原因為坊絲整理劑更容易由低度分解之纖維喪失。發現 與本發明之隈離子纺絲整理劑(參見實例5及6)相同的 丹尼數。 實例4中抗靜電劑為脂肪酸/聚胺縮合產物(其中R1 為二亞甲基硬脂酸_之式]I化合物,Μ乙酸根作為相對雛 子)而親水潤滑劑為乙氧化脂肪酿。纗維顯示性質良好但 再度溼潤性稍高。 實例5及6中抗靜電劑為脂肪酸/聚胺縮合產物(如 實例4)而親水潤滑劑為親水脂肪酸烷氧化物。實例5之 纖维表面分解係利用低的冷卻空氣速度進行,而實例6之 速度較高。此種實例顯示控制分解程度之重要性,由於雖 然實例5具高度分解之纘維顯示良好擊穿及再度溼潤性質 ^ 产/Φ訂 為 (,請先閲讀背面之注意事項再填寫本X ) 本紙張尺度適用中國國家標準(CNS ) Α4规格(210X2.97公釐) -2Ί — 313595 A7 B7 五、發明説明(25 ) ,但強度性質不良。 實例7之纖維係使用實例5及6相同纺絲整理劑成分 Μ生產規模生產。此等纖維就親水性之持久性K及就強度 而言皆顯示良好性質。 (請先閱讀背面之注意事項再填寫本頁) 經濟部中央標準局員工消費合作社印製 28 本紙張尺度適用中國國家標準(CNS〉Α4規格(210Χ297公釐)MD CD BL · Printed by the Ministry of Economic Affairs, Central Bureau of Standards, Employee Consumer Cooperatives A7 B7 V. Description of the invention (24) Notes to examples Example 1 (Comparative example) A typical modified (ethoxylated) polysiloxane wire finishing agent is used, the fiber has Relatively low Danny number and moderate rewetting. The durability of the system is quite good. The spinning green finishing agent contains about 3 (3% modified polysiloxane, most of the antistatic agent is ethoxylated fatty acid salt. Example 2 (comparative example) uses the same antistatic ingredients as in example 1, but the polysilicone has an interface Active agent substitution. Durability and tango number are not good enough, but the fiber properties are still satisfactory. Examples 3.1, 3.2 and 3.3 (comparative examples) show that by increasing the polymer melt temperature (295 ¾, 3 0 0 ¾ and 3 0 5 ¾) At the same time, the cooling air and other conditions are kept constant, and the resulting fiber surface is decomposed. The amount of Fangjiang finishing agent applied to irrigation and maintenance can increase with the increase of fiber surface decomposition. The possible reason is that Fangsi finishing agent is easier Loss of fibers from low decomposition. Found the same Danny number as the Kuma ion spinning finishing agent of the present invention (see Examples 5 and 6). The antistatic agent in Example 4 is a fatty acid / polyamine condensation product (where R1 is two Methylene stearic acid_formula] I compound, M acetate as a relative chick) and the hydrophilic lubricant is ethoxylated fat brewing. Yiwei showed good properties but slightly higher wettability. Antistatic agent in Examples 5 and 6 Fatty acid / polyamine condensation The product (such as Example 4) and the hydrophilic lubricant is a hydrophilic fatty acid alkoxide. The fiber surface decomposition of Example 5 is carried out using a low cooling air speed, while the speed of Example 6 is higher. This example shows the importance of controlling the degree of decomposition Because of the fact that Example 5 has a highly decomposed dimensional display showing good breakdown and re-wetting properties ^ Production / Φ is set to (, please read the precautions on the back before filling in this X) This paper scale is applicable to the Chinese National Standard (CNS) Α4 specification (210X2.97mm) -2Ί — 313595 A7 B7 5. Description of the invention (25), but the strength properties are poor. The fiber of Example 7 is produced on the production scale using the same spinning finishing agent component M of Examples 5 and 6. This Such fibers have good properties in terms of hydrophilicity, durability K, and strength. (Please read the notes on the back before filling this page) Printed by the Employees ’Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 28 This paper standard applies to China ’s national standards (CNS> Α4 specification (210Χ297mm)

Claims (1)

;1359〇 A8 B8 C8 D8; 1359〇 A8 B8 C8 D8 經濟部中央標準局員工消費合作社印製 六、申請專利範圍 第84104174號專利申請案申請專利範圍修正本 修正日期:86年3月 1. 一種可梳理之以親水聚烯烴為主的短纖維之製造方法 ,該短纖維在以水或水性液體溼潤一次後仍可大體上 •維持其親水性,該方法包含有下列步驟: a .對經紡絲的長纖維施加以至一包含有一種親水潤 滑劑之第一紡絲整理劑, b. 拉伸長該等纖維, c. 將拉伸後的長纖維施加以至一包括有一種陽離子 抗靜電劑之第二紡絲整理劑, d. 捲曲該等長纖維, e. 乾燥該等長纖雒,以及 f .切割長纖維,俾以獲得親水短纖維; 該等親水_短纖維當藉由EDANA所建議的非織物吸收試 驗(第10 .1 -72號)予以測定時,具有一至多分為1 鐘之液體吸收時間,該測定傺使用具有10g/m2的基重 之梳理纖維網並以15 m/ m i η來梳理纖維而製備桿的 維樣品。 2. 如申請專利範圍第1項之方法,其中該第一紡絲整理 劑進一步包括有一種陽離子抗靜電劑。 3 .如申請專利範圍第1項之方法,其中該第二紡絲整理 劑進一步包括有一種親水潤滑劑。 4 .如申請專利範圍第1項之方法,其中該親水潤滑劑偽 選自烷氣化醇類,烷氧化酯類及烷氧化醛胺類。 本紙張尺度適用中國國家揉準(CNS ) A4规格(210X297公釐) ·(請先K讀背面之注意事項再填寫本頁) ·I Inti mu I ml nfn—1 fm 0¾. A8 B8 C8 DB 經濟部中央榡準局員工消費合作社印裝 六、申請專利範圍 5.如申請專利範圍第1項之方法,其中該親水潤滑劑為 一具有通式I的化合物 R1 X' ! zMCH2)n-[N+-(CH2)Jm-Z2 1 I R2 其中 Z1 及 Z2 為 Alk-C ⑽ Η-、iAlk)2-N-、Aik-COO-或 Η ,其中Aik為一含有1至24個碩原子之直鏈脂族烷基 或烷烯基或是由該於等基團所構成的混合物, 但規定Z1及Z2不可皆為Η ; R1為Η、CH3、具有2至24 個硕原子數之烷基或二亞甲基脂肪酸酯;P為Η或CH3 ;11為1至4之間的整數;m為1至10之間的整數;χ-為 相對離子。 6 .如申請專_利範圍第5項之方法,其中在該具有式I之 化合物中,Aik為一含6-14値碳原子之烷基;及χ-為 乙酸根、檸檬酸根、乳酸根、偏硫酸根或氯離子。 7. 如申請專利範圍第1項之方法,其中該陽離子抗靜電 劑僳選自胺類、醯胺類與烷氣化之化合物。 8. 如申請專和範圍第7項之方法,其中該陽離子抗靜電 劑像選自烷氧化之胺類與醯胺類中。 9 .如申諳專利範圍第1項之方法,其中該陽離子抗靜電 劑為一具有通式I[的化合物 本紙張尺度適用中國國家捸準(CNS ) A4規格(210X297公釐) m ms n^— m I •(請先陴讀背面之注意事項再填寫本頁) in I ----: I ......I ^^1. I --1 «ml tma · ABCD 313595 六、申请專利範圍 R1 X— J 'r3_[〇- (CH2) ^-0-(〇Η2)π-[ν+- (CH2) Jm-0-[(CH2)x-〇L-R3 : R2 其中R1為H、.CH3、含1至24個磺原子之烷基或二亞甲 基脂肪酸酯;R2為Η或CH3;R3各自為甲基、乙基 或Aik-羰基,其中Aik為一含2至24個碳原子之直鍵 脂族之烷基或烷烯基或是由該等基團所構成的混合物 ;«為1至4之間的整數;m為1至10之間的整數;X為2 或3 ; y及z分別為大於〇之整數,y與z之總合至少為5 ;&amp; X-為相對離子。 10. 如申請專利範圍第9項之方法,其中在具通式I之化 合物中,Aik傺為一含6-14個碩原子之烷基;當R3為 烷基時,_R3為含6-14個碩原子之烷基;及X-為乙酸根 、檸稼酸根、乳酸根、偏硫酸根或氯離子。 11. 如申請專利範圍第9項之方法·其中該陽離子抗靜電 劑具有至多約為1〇〇〇之分子量.。 12. 如申請專利範圍第1項之方法,其中該第一與/或第 二紡絲整理劑,基於該第一與或第二紡絲整理劑之活 性成分含量,各自地包含有一含量在0至5%重量比之 間的聚二有機矽氣烷化合物。 13. 如申請專利範圍第1項之方法,其中該第一與/或第 二紡絲整理劑,基於該第一與或第二紡絲整理劑之活 性成分含量,各自地包含有一含量在0至1%重量比之 本紙張尺度適用中國國家橾率(CNS ) A4规格(210X297公釐) ·.(請先閣讀背面之注意事項再填寫本頁) 装丨 —fn n ml tmwaml · 經濟部中央標準局負工消費合作社印製 '•Jr, ABCD 經濟部中央標準局員工消費合作社印裝 、申請專利範圍 間的聚二有機矽氣烷化合物。 14. 如申請專利範圍第1項之方法,其中該第一及第二纺 絲整理劑大體上不含有聚二有機矽氣烷化合物。 15. 如申請專利範圍第1項之方法,其中相同的紡絲整理 劑組成物偽被使用作為該第一紡絲整理劑及該第二纺 絲整理劑。 16. 如申請專利範圍第1項之方法,其中該第二紡絲整理 劑,基於其活性成分含量,包含有一作為調節摩擦力 之潤滑劑用且具有一在40-120°C之範圍内的熔點之0 至10%童量比的天然或合成烴蠟,或一包含一種該烴 蠘並具有在40-120°C範圍内之熔點的蠟混合物。 .17.如申請專利範圍第16項之方法,其中該烴蟠或蟠混合 物具有一在40-90°C之範圍内的熔點。 18. 如申請專利範圍第2或3項之方法,其中該第一及第 二纺絲整理劑之活性成分含量,傺包括有低於100%但 不高於50¾之一種或多種潤滑劑以及大於0但不高於50 %之一種或多種抗靜電劑以及/或乳化劑。 19. 如申請專利範圍第18項之方法,其中該第一及第二紡 絲整理劑之活性成分含量,傜包括有低於100¾但不高 於65¾之一種或多種潤滑劑以及大於0但不高於35%之 一種或多種抗靜電劑以及/或乳化劑。 20. 如申請專利範圍第1項之方法,其中該纖維為聚丙烯 纖維。 21. 如申請專利範圍第20項之方法,其中該1^1〃1)^3 本纸張尺度適用中國國家樣準(CNS ) A4規格(210X297公釐) •(請先闐讀背面之注意事項再填寫本頁) ^ . In 訂 丨&lt; • m - -1 I 1 I - ---. 5 9 5 S ί 7J ABCD 經濟部中央標準局員工消費合作社印裂 六、申請專利範圍 /1&gt;4]711»4«111^&lt;;1^;11比值涤在2.4-3.0之範圍内。 22‘如申諳專利範圍第〗項之方法,其中由該纖維所製備 之梳理纖維網•當藉由EDANA對非織物吸收性建議試 驗(第10.1-72號)測得時,具有一至多為30秒之液 體吸收時間。 23. 如申請專利範圍第22項之方法,其中由該纖維所製備 之梳理纖維網,當藉由EDAHA對非織物趿收性建議試 驗(第10.1-72號)測得時,具有一至多為10秒之液 體吸收時間。 24. —種變形可梳理之以聚烯烴為主的短纖維,其傜依據 申請專利範圍第1至23項中任一項之方法來製得的。 25. —種變形可梳理之以聚烯烴為主的短纖維,於其表面 上載有一層包括有一種陽離子抗靜電劑及一種親水潤 滑劑之紡'絲整理劑塗膜,該紡絲整理劑塗膜.,基於紡 絲整理劑塗膜重量,包含有0至5%重量比之聚二有機 矽氧烷化合物,該纖維具有一變形程度與均勻度,以 使在100 in/分鐘之速度下足夠被梳理成一非織材料 &gt;其為一具20 g/m2基重之非織物時具有下述特性: a. 藉由基於EDANA標準編號ERT 150.2-93之經修改 的ED AN A試驗方法,其被稱為「3X擊穿方法」 ,所測得第三次擊穿時間至多為20秒; b. 於「3 X 10¾方法」之分數為28-30 ; 〇.根據£0 — 1\標準編號£1^151.0-93所測得再度溼 澗性至多為〇. 3g ;以及/或 -5 - 本紙張尺度適用中國國家標準(CNS ) A4规格(210 X 297公釐) ·(請先¾讀背面之注意事項再填寫本頁) 訂 Λ》· In ml in uwPrinted by the Employee Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs. 6. Scope of Patent Application No. 84104174. Application for amendment of patent scope. Date of amendment: March, 86. 1. Manufacturing of a cardable staple fiber mainly made of hydrophilic polyolefin Method, the short fiber can be substantially wetted with water or an aqueous liquid once • Maintain its hydrophilicity, the method includes the following steps: a. Apply to the spun long fiber to one containing a hydrophilic lubricant The first spinning finishing agent, b. Stretch the long fibers, c. Apply the stretched long fibers to a second spinning finishing agent including a cationic antistatic agent, d. Curl the long fibers , E. Drying the long fibers, and f. Cutting the long fibers, so as to obtain hydrophilic short fibers; these hydrophilic _ short fibers should pass the non-woven absorption test recommended by EDANA (No. 10.1-72) When the measurement is performed, it has a liquid absorption time of one to at most 1 minute. This measurement uses a carded fiber web having a basis weight of 10 g / m2 and carded the fibers at 15 m / mi η to prepare a dimensional sample of the rod. 2. The method as claimed in item 1 of the patent application, wherein the first spinning finishing agent further includes a cationic antistatic agent. 3. The method as claimed in item 1 of the patent application, wherein the second spinning finishing agent further comprises a hydrophilic lubricant. 4. The method as claimed in item 1 of the patent application, wherein the hydrophilic lubricant is pseudo-selected from alkylated alcohols, alkoxylated esters and alkoxylated aldols. This paper scale is applicable to China National Standard (CNS) A4 (210X297mm) · (Please read the notes on the back side before filling in this page) · I Inti mu I ml nfn—1 fm 0¾. A8 B8 C8 DB Economy Printed and printed by the Employees 'Consumer Cooperative of the Central Bureau of Prefectural Affairs of the Ministry 6. Scope of patent application 5. The method as described in item 1 of the patent application, in which the hydrophilic lubricant is a compound of the general formula I R1 X'! ZMCH2) n- [N + -(CH2) Jm-Z2 1 I R2 where Z1 and Z2 are Alk-C ⑽ Η-, iAlk) 2-N-, Aik-COO- or Η, where Aik is a straight chain containing 1 to 24 large atoms Aliphatic alkyl or alkenyl group or a mixture of such equivalent groups, but Z1 and Z2 must not be both Η; R1 is Η, CH3, an alkyl group with 2 to 24 atoms or two Methylene fatty acid ester; P is Η or CH3; 11 is an integer between 1 and 4; m is an integer between 1 and 10; χ- is a relative ion. 6. The method as claimed in item 5 of the patent application, wherein in the compound of formula I, Aik is an alkyl group containing 6 to 14 carbon atoms; and χ- is acetate, citrate, lactate , Metasulfate or chloride ion. 7. The method as claimed in item 1 of the patent application, wherein the cationic antistatic agent is selected from the group consisting of amines, amides, and alkane compounds. 8. The method as specified in item 7 of the scope of application, wherein the cationic antistatic agent is selected from alkoxylated amines and amides. 9. The method as claimed in item 1 of the patent scope, wherein the cationic antistatic agent is a compound of the general formula I [This paper standard is applicable to the Chinese National Standards (CNS) A4 specifications (210X297 mm) m ms n ^ — M I • (please read the notes on the back before filling in this page) in I ----: I ...... I ^^ 1. I --1 «ml tma · ABCD 313595 VI. Application Patent scope R1 X — J 'r3_ [〇- (CH2) ^ -0- (〇Η2) π- [ν +-(CH2) Jm-0-[(CH2) x-〇L-R3: R2 where R1 is H, .CH3, alkyl or dimethylene fatty acid esters containing 1 to 24 sulfonic atoms; R2 is Η or CH3; R3 is each methyl, ethyl or Aik-carbonyl, where Aik is a A straight bond aliphatic alkyl or alkenyl group of 24 carbon atoms or a mixture of these groups; «is an integer between 1 and 4; m is an integer between 1 and 10; X is 2 or 3; y and z are integers greater than 0, respectively, the sum of y and z is at least 5; & X- is a relative ion. 10. The method as claimed in item 9 of the patent scope, wherein in the compound of general formula I, Aik is an alkyl group containing 6-14 master atoms; when R3 is an alkyl group, _R3 contains 6-14 An alkyl group with a large atom; and X- is acetate, citrate, lactate, metasulfate or chloride. 11. A method as claimed in item 9 of the patent application range, wherein the cationic antistatic agent has a molecular weight of at most about 1,000. 12. The method as claimed in item 1 of the patent application, wherein the first and / or second spinning finishing agent, based on the active ingredient content of the first and / or second spinning finishing agent, each contains a content of 0 Polydiorganosilane compounds between 5% and 5% by weight. 13. The method as claimed in item 1 of the patent application, wherein the first and / or second spinning finishing agents, based on the active ingredient content of the first and / or second spinning finishing agents, each contain a content of 0 The paper standard of up to 1% by weight is applicable to China ’s National Atomic Rate (CNS) A4 specification (210X297mm). (Please read the precautions on the back before filling this page) 装 ——fn n ml tmwaml · Ministry of Economic Affairs Printed by the National Bureau of Standards' Consumer Labor Cooperatives' • Jr, ABCD Polydiorganosilane compound printed and patented between employees' consumer cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs. 14. The method as claimed in item 1 of the patent application, wherein the first and second spinning finishing agents do not substantially contain polydiorganosilane compounds. 15. The method as claimed in item 1 of the patent application, wherein the same spinning finish composition is used as the first spinning finish and the second spinning finish. 16. The method as claimed in item 1 of the patent scope, wherein the second spinning finishing agent, based on the content of its active ingredients, contains a lubricant for adjusting friction and has a range of 40-120 ° C A natural or synthetic hydrocarbon wax with a melting point of 0 to 10%, or a wax mixture containing one of these hydrocarbon worms and having a melting point in the range of 40-120 ° C. .17. The method as claimed in item 16 of the patent application, wherein the hydrocarbon pan or pan mixture has a melting point in the range of 40-90 ° C. 18. The method as claimed in item 2 or 3 of the patent application, wherein the active ingredient content of the first and second spinning finishing agents, including one or more lubricants with less than 100% but not more than 50¾, and greater than 0 but not more than 50% of one or more antistatic agents and / or emulsifiers. 19. The method as claimed in item 18 of the patent application, wherein the active ingredient content of the first and second spinning finishing agents includes one or more lubricants less than 100¾ but not more than 65¾ and more than 0 but not One or more antistatic agents and / or emulsifiers higher than 35%. 20. The method as claimed in item 1 of the patent application, wherein the fiber is polypropylene fiber. 21. For example, the method of claim 20, where the 1 ^ 1〃1) ^ 3 paper size is applicable to China National Standards (CNS) A4 specification (210X297mm) • (Please read the note on the back first Please fill out this page again ^ ^. In Order 丨 <m--1 I 1 I----. 5 9 5 S ί 7J ABCD Ministry of Economic Affairs Central Standards Bureau Employee Consumer Cooperative Printed, Patent Application Scope / 1 &gt;; 4] 711 »4« 111 ^ &lt;; 1 ^; 11 ratio is in the range of 2.4-3.0. 22 'The method as claimed in Item〗 of the patent scope, in which the carded fiber web prepared from the fiber has a maximum of 1 when measured by the EDANA recommended test for non-woven fabric absorption (No. 10.1-72) 30 seconds of liquid absorption time. 23. The method as claimed in item 22 of the patent application, in which the carded web prepared from the fiber, when measured by EDAHA on the non-woven fabric recommendability test (No. 10.1-72), has one to at most 10 seconds of liquid absorption time. 24. A type of deformable cardable staple fiber mainly made of polyolefin, which is produced by the method of any one of items 1 to 23 of the patent application. 25. A kind of deformable and combable staple fiber mainly made of polyolefin, on the surface of which is loaded a coating film of a spinning finishing agent including a cationic antistatic agent and a hydrophilic lubricant, which is coated with the spinning finishing agent Membrane., Based on the weight of the spinning finishing agent coating film, containing a polydiorganosiloxane compound in a weight ratio of 0 to 5%, the fiber has a degree of deformation and uniformity so that it is sufficient at a speed of 100 in / min Carded into a non-woven material> It is a non-woven fabric with a basis weight of 20 g / m2 and has the following characteristics: a. By the modified ED AN A test method based on EDANA standard number ERT 150.2-93, which Known as the "3X breakdown method", the measured third breakdown time is at most 20 seconds; b. The score in the "3 X 10¾ method" is 28-30; 〇. According to the £ 0 — 1 \ standard number £ 1 ^ 151.0-93 The measured re-wetness is at most 0.3g; and / or -5-This paper scale applies the Chinese National Standard (CNS) A4 specification (210 X 297mm) · (please read ¾ Note on the back then fill out this page) Order Λ》 · In ml in uw 申請專利範圍 經濟部中央樣準局員工消費合作社印製 d.藉EDANA對非織物吸收性推薦試驗(编號10.1-72)所測得液體吸收時間至多為1分鐘。 2δ·$Πφ請專利範圍第25項之變形可梳理之以聚烯烴主為 的短纖維,其為一具20 s/m2基重之非織物時具有下 述特性: a .所測得第三次擊穿時間至多為10秒; b. 再潤性至多為O.lg ;以及/或 c. 液體吸收時間至多為1分鐘。 27, 如申請專利範匿第25項之纖雒,其中該親水潤滑劑僳 如申請專利範圍第4項中所定義者。 28. 如申請專利範菌第25項之纖維,其中該陽離子抗靜電 劑係如申請專利範圍第7項中所定義者。 29 .—種親水非織材料,其包含有如申請專利範圍第25項 之纖維。' ’‘ 30 .如申請專利範圍第29項之親水非織材料,其於溼潤後 仍大體保有如下所界定之親水特性: a. .藉由基於EDANA標準编號ERT 150.2-93之經修改 的EDANA試驗方法,其被稱為「3 X擊穿方法」 ,所測得第三次擊穿時間至多20秒,; b. 於「3 X 10孔方法」之分數為28-30 ;以及/或 c. 根據EMNA標準编號ERT 151.0-93所測得再度溼 潤性至多為〇.3g。 31. —種親水非織材料’其包含有如申諳專利範圍第27項 之纖維。 -6 - . 本紙張尺度逋用中國國家標準(CNS ) A4規格(21〇Χ297公釐) t請先¾讀背面之注意事項再填寫本頁) 裝-- ---.訂 -C i--^----- em— —^1— m· 經濟部中央標準局貞工消費合作社印製 323595 λβ Βδ C8 _-__ 六、申請專利範圍 32 .如申請專利範圍第31項之親水非織材料’其於淫潤後 仍大髏保有如下所界定之親水特性: a. 藉由基於ED AN A標準編號ERT 150. 2-93之經修改 的EDANA試驗方法,其被稱為「3 X擊穿方法」 ,所測得第三次擊穿時間至多為20秒; b. 於「3X10孔方法」之分數為28-30;以及/或 &lt;:.根據£0&amp;1^標準编號〖}^151.0-93所測得再度溼 潤性至多為〇.3g。 33. —種親水非織材料,其包含有如申請專利範圍第2δ項 之纖維。 34. 如申請專利範圍第33項之親水非織材料,其於溼潤後 仍大體保有下述之親水特性: a. 藉由基於EDANA標準編號ERT 150. 2-93之經修改 的ED’ANA試驗方法,其被稱為「3X擊穿方法」 ,所測得第三次擊穿時間至多為20秒; b. 於「3 X 10孔方法」之分數為28-30 ;以及/或 c. 根據ED ANA標準編號ERT .151.0-9 3所測得再度溼 潤性至多為〇.3g。 35·—種製造可再溼潤之親水非織材料的方法,其包括加 工一如申請專利範圍第25項之纖維,以獲得黏合用之 纖維網,並將所得纖維網黏合,以獲得該非織材料。 36 . —種製造可再溼潤之親水非織材料的方法,其包括加 工一如申請專利範圍第27項之纖維,以獲得黏合用之 纖維網,並將所得纖維網黏合,以獲得該非織材料。 本紙浪尺度適用中國國家揉準(CNS ) A4規格(210X297公釐) t請先皞讀背面之注意事項再填寫本頁) —f 裝—— 訂 313595 ABCD 申請專利範圍 37.—種製造可再溼潤之親水非織材料之方法,其包括加 工一如申請專利範圍第28項之纖維,以獲得黏合用之 纖維網,並將所得纖維網黏合,以獲得非織材料。 請先降讀背面之注意事項再填寫本頁) ---f 裝-- 訂 經翁' 部t 央 標 準為 員 工 消 費 合在 印 製 本紙張尺度適用中國國家揉準(CNS ) A4说格(210 X 297公釐)Scope of patent application Printed by the Employee Consumer Cooperative of the Central Prototype Bureau of the Ministry of Economic Affairs d. The liquid absorption time measured by EDANA's recommended test for non-woven fabric absorption (No. 10.1-72) is at most 1 minute. 2δ · $ ΠφThe deformation of item 25 of the patent scope can be carded as a staple fiber mainly made of polyolefin, which is a non-woven fabric with a basis weight of 20 s / m2 and has the following characteristics: a. The measured third The secondary breakdown time is at most 10 seconds; b. Rewetting is at most O.lg; and / or c. Liquid absorption time is at most 1 minute. 27. For example, the fibrous molybdenum in patent application No. 25, wherein the hydrophilic lubricant is as defined in item 4 of the patent application scope. 28. For example, the fiber of patent application bacteria No. 25, wherein the cationic antistatic agent is as defined in item 7 of the patent application scope. 29.—A hydrophilic non-woven material, which contains fibers as described in item 25 of the patent application. '' '30. The hydrophilic nonwoven material as claimed in item 29 of the patent application, after wetting, still retains the hydrophilic characteristics as defined below: a .. by the modified EDANA standard number ERT 150.2-93 EDANA test method, which is called "3 X breakdown method", the measured third breakdown time is at most 20 seconds; b. The score of "3 X 10 hole method" is 28-30; and / or c. The rewetting measured according to EMNA standard number ERT 151.0-93 is at most 0.3g. 31. —A hydrophilic non-woven material ’which contains fibers such as item 27 of the patent application. -6-. This paper uses the Chinese National Standard (CNS) A4 specification (21〇Χ297mm) t Please read the precautions on the back and then fill out this page) Install----. Subscribe-C i- -^ ----- em— — ^ 1— m · Printed 323595 λβ Βδ C8 _-__ by Zhengong Consumer Cooperative of Central Bureau of Standards of the Ministry of Economic Affairs VI. Patent application scope 32. For example, the hydrophilic scope of the patent application item 31 The woven material's skeletal body retains its hydrophilic properties as defined below after being moistened: a. By the modified EDANA test method based on ED AN A standard number ERT 150. 2-93, it is called "3 X "Breakthrough method", the measured third breakdown time is at most 20 seconds; b. The score in the "3X10 hole method" is 28-30; and / or &lt;:. According to £ 0 &amp; 1 ^ standard number 〖} ^ 151.0-93 measured again wettability is at most 0.3g. 33. A hydrophilic non-woven material, which contains the fiber as specified in item 2δ of the patent application. 34. If the hydrophilic non-woven material in the 33rd scope of the patent application, it still retains the following hydrophilic properties after wetting: a. By the modified ED'ANA test based on EDANA standard number ERT 150. 2-93 Method, which is called "3X breakdown method", the measured third breakdown time is at most 20 seconds; b. The score of "3 X 10 hole method" is 28-30; and / or c. According to ED ANA standard number ERT.151.0-9 3 measured again wettability is at most 0.3g. 35 · —A method for manufacturing a rewetable hydrophilic nonwoven material, which includes processing fibers as claimed in item 25 of the patent application range to obtain a fiber web for bonding, and bonding the resulting fiber web to obtain the nonwoven material . 36. A method of manufacturing a rewetable hydrophilic nonwoven material, which includes processing fibers as claimed in item 27 of the patent application to obtain a bonding web, and bonding the resulting web to obtain the nonwoven . The size of this paper is suitable for China National Standard (CNS) A4 (210X297mm) t Please read the precautions on the back and then fill out this page) —f Packing——Subscribe to 313595 ABCD patent application scope 37.-manufacturable remanufacturable A method of moistening hydrophilic non-woven material includes processing fibers as claimed in item 28 of the patent application to obtain a fiber web for bonding, and bonding the resulting fiber web to obtain a non-woven material. Please read the precautions on the back first and then fill out this page) --- f 装 装-碼 经 翁 'Department t Central standard is for the consumption of employees in the printed paper standard applicable to China National Standard (CNS) A4 210 X 297 mm)
TW084104174A 1995-04-21 1995-04-27 TW313595B (en)

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Publication number Priority date Publication date Assignee Title
EP0852268B1 (en) * 1996-12-04 2002-08-21 Fibertech Group, Inc. Absorbent articles having improved separator layer
EP0951913A1 (en) * 1998-04-22 1999-10-27 The Procter & Gamble Company High liquid suction absorbent structures with permanently hydrophilic meltblown non-woven wrap sheet with small diameter fibers
EP1614790B1 (en) 2004-07-09 2008-10-08 JOHNSON & JOHNSON GmbH An absorbent personal care product for cosmetic and/or dermatological applications comprising at least one absorbent sheet

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GB1250917A (en) * 1967-12-30 1971-10-27
US4020212A (en) * 1974-09-13 1977-04-26 Phillips Petroleum Company Polyolefin fibers useful as fiberfill treated with finishing agent comprising an organopolysiloxane and a surface active softener
DE3100803A1 (en) * 1981-01-13 1982-08-05 Wacker-Chemie GmbH, 8000 München AGENT FOR INCREASING THE SLIDABILITY OF ORGANIC FIBERS
NZ230238A (en) * 1988-08-12 1991-10-25 Colgate Palmolive Co Fabric softening composition comprising a cationic softening salt and a cross-linked polysiloxane
US5045387A (en) * 1989-07-28 1991-09-03 Hercules Incorporated Rewettable polyolefin fiber and corresponding nonwovens

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