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TW476833B - Shrink-proof treatment of cellulosic fiber textile - Google Patents

Shrink-proof treatment of cellulosic fiber textile Download PDF

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Publication number
TW476833B
TW476833B TW86106821A TW86106821A TW476833B TW 476833 B TW476833 B TW 476833B TW 86106821 A TW86106821 A TW 86106821A TW 86106821 A TW86106821 A TW 86106821A TW 476833 B TW476833 B TW 476833B
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Taiwan
Prior art keywords
treatment
caustic
cellulose
hot water
textile
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TW86106821A
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Chinese (zh)
Inventor
Yuichi Yanai
Takayuki Hirai
Masayoshi Oba
Kiyoshi Ikeda
Yasushi Takagi
Original Assignee
Nisshin Spinning
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Priority claimed from JP08260166A external-priority patent/JP3073446B2/en
Priority claimed from JP26016996A external-priority patent/JP3073447B2/en
Priority claimed from JP26249096A external-priority patent/JP3154149B2/en
Application filed by Nisshin Spinning filed Critical Nisshin Spinning
Application granted granted Critical
Publication of TW476833B publication Critical patent/TW476833B/en

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  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

A method for shrink-proofing a cellulosic fiber textile that involves liquid ammonia treatment, hot water or caustic alkali treatment under tension or under no tension, and with optional resin treatment.

Description

476833 A7 B7 五、發明説明(1 ) 發明背景 發明領域 本發明有關一種纖維素纖維紡織品防縮處理用之方法 。更特別的是,其有關用以處理纖維素纖維紡織品之方法 ,使該紡織品完全防縮,不會有基本强度之損失,因此其 於清洗後造成之收縮最小且重覆清洗後硬化之手感最小。 先前技藝 迄今,因爲具有調節濕氣吸收作用,手感質地良好及 易處理等優點,纖維素纖維紡織品已廣泛充作衣物材料。 然而,此種纖維素纖維紡織品在清洗後會收縮且重覆清洗 後有手感硬化之問題。 經濟部中央標準局員工消費合作社印製 (請先閲讀背面之注意事項再填寫本頁) 清洗後收縮之原因與二種現象有關。現象之一係機織 針織物在製造和處理過程中因種種因素而變形。更詳細地 說,·清洗時機織針織物在無外力的自由狀態下被扔擲扭轉 ,其易於回到原始安定狀態,因而招致收縮。此種收縮作 用可以藉由機械方法避預防,諸如以機械預縮處理爲代表 。此方法使用橡膠帶或毛氈層式預縮機器,物理性連續壓 縮該纖維使其收縮而降低該纖維之收縮可能性,賦予其防 縮性。然而,此方法無法充分降低厚纖維布匹或堅硬的最 終纖維收縮可能性。 另一現象係機織針織物的收縮係個別纖維吸水潤脹而 增加其剖面積之結果。此收縮作用係因吸收水而產生。該 纖維乾燥去除水分之後,纖維組織無法自行回復到潤脹前 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 476833 A7 B7 五、發明説明(2 ) 之原有體稹。該纖維維持收縮狀態。 發明摘要 本發明係提出一種用以處理纖維素纖維紡織品之方法 ,使其充分防縮而不會有强度之實質損失,如此其於清洗 後之收縮最小化,而重覆清洗後手感硬化情形最小化。 本發明者已發現藉由液態氨處理纖維素纖維紡織品, 而後在伸展或非伸展狀況下以熱水或苛性鹼處理該纖維紡 織物,則該纖維素纖維紡織物可以充分防縮,如此其於清 洗後所產生之防縮最小化而重覆清洗後手感硬化最小化。 其在無實質强度損失下完成。 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 更詳細地說,以液態氨預浸纖維素纖維紡織品時,該 液態氨不僅滲入非晶相區域,亦滲入纖維素之結晶區域, 使該氫鍵斷裂,因此使得纖維整體潤脹。其後,進行熱處 理以蒸發氫鍵新近形成處之液態氨,至少一部分結晶區域 產生纖維素III結晶結構。該結晶被固定於潤脹狀態。此結 果降低結晶度。當此種纖維以樹脂作最終處理時,防皺和 防縮性質得到改善,而强度稍有損失。此事實係本技藝中 已知者。 相對地,液態氨處理之後,藉由以熱水或苛性鹼處理 纖維素纖維紡織品,纖維素III結晶結構復原成纖維素I或 II之結晶結構,該過程期間因爲熱水或苛性鹼滲透之故, 仍保持潤脹狀態。然後,該纖維結構固定爲潤脹且鬆弛。 因此,因清洗而受水潤脹和伸展鬆弛作用之影響最小化或 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 476833 A7 B7 五、發明説明(3 ) 者被消除。防縮處理係以此種方式完成。 隨後在此種如此處理之纖維素纖維紡織品上作樹脂處 理,與樹脂處理前相較,可賦予其經改良之防皺或防縮性 ,而且無實質强度損失。 更詳細地說,先前技藝之纖維素纖維紡織品之樹脂處 理具有樹脂添加量增加,防皺性或防縮性質改善,但是抗 張强度同時下降之傾向。當抗張强度降低時,可以藉由使 纖維素纖維之間交聯而定安該氫鍵,而達成防皺和防縮性 質改善,此係因交聯導入致使有區域性脆性破裂的可能。 此等狀況彼此矛盾。必須找出一種改善防縮性和避免强度 損失之折衷辦法。因爲纖維素纖維具有包括結晶和非晶相 部分或者表皮與內部部分等多相結構,必須使交聯基均勻 分佈以避免强度損失。 經濟部中央榡準局員工消費合作衽印製 (請先閱讀背面之注意事項再填寫本頁) 此種需求在下文中得到滿足。當已經經由液態氨處理 而充分潤脹之纖維在伸展或非伸展下以熱水或苛性鹼處理 時,該潤脹狀態下之纖維結構產生某些改變以改良纖維之 可及度,使具有交聯點之理想結晶結構儘可能均勻分佈, 達成防皺性或防縮性之改良。當此狀態下之纖維進一步以 樹脂處理時,少量樹脂就足以改良防縮性質。樹脂添加量 愈少則强度損失愈少。以此種方式可以達到上述相互矛盾 需求之間的合理折衷方法。 本發明防縮處理方法有利於製造充分防縮之纖維素纖 維紡織品,而不會造成强度的實質損失,其於清洗後之收 縮作用最小化而且重覆清洗後手感硬化最小化。特別是, 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 476833 A7 B7 五、發明説明(4 ) 可使棉,麻,嫘縈等薄,强度低之紡織品具有經改良之防 縮性或防皺性,使其維持實際上可接受强度。 因此,本發明提出一種纖維素纖維防縮處理用之方法 ,其包括以液態氨處理該纖維紡織品,然後在伸展或非伸 展下以熱水或苛性鹼處理該纖維紡織品,選擇性以樹脂處 理該纖維結織品。 發明詳沭 本發明防縮處理方法包括步驟(1 ),以液態氨處理 纖維素纖維紡織品,以及步驟(2 )在伸展或非伸展狀況 下,以熱水或苛性鹼處理該纖維紡織品。 i 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 可以採用本發明方法處理之纖維素纖維紡織品係由包 括天然纖維和再生纖維素纖維之纖維素纖維構成,例如棉 花,大麻,嫘縈,波里諾西克,銅銨纖維以及高强度再生 纖維素纖維(例如,市售商標爲天絲(Te nee 1 )者)。此 等天然纖維和再生纖維素纖維可爲混合纖維材料形式,其 係與其匕纖維’諸如合成纖維’通常爲聚酯類和聚醯胺類 摻和製得。該混合纖維材料必須具有較多含量之纖維素纖 維較佳,纖維素纖維含量至少5 0重量%更佳。該鹼處理 可以針對不溶於所使用之鹼溶液的纖維進行。 本文可使用之纖維素纖維紡織品包括機織纖維,針織 品和不織纖維。若情況需要,可對該紡織品進行預處理, 諸如燒毛處理,退漿處理,煮練,漂白以及絲光處理。該 紡織品亦可經染色或印花處理。 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) 476833 A7 B7 五、發明説明(5 ) 首先,以液態氨處理該纖維素纖維紡織品,其係在大 氣壓力維持- 3 3 °C或更低溫度下以液態氨預浸該紡織品 。該預浸作用意義包括,浸於液態氨中,噴洒液態氨以及 塗覆液態氨。預浸時間可在大約5至4 0秒範圍內適當選 擇0 液態氨最常用以引發纖維素纖維紡織品中之纖維素I 或II轉變成纖維素ΠΙ之作用,然而若情況需要可使用低級 烷基胺類,諸如甲胺和乙胺。該過程結束時,藉由加熱自 經液態氨處理之纖維素纖維紡織品中去除該氨。 該液態氨處理致使纖維素I或II之結晶體結構依預浸 時間成比例轉變成纖維素III結晶。預浸時間爲5秒時,纖 維素III結晶結構佔整體結晶達到大約1 0 %,8秒鐘時約 爲15%,12秒鐘時2 5%,1 8秒鐘時約爲3 5%, 而且2 0秒或更長時間下約爲4 0%。 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) •在液態氨處理後進行熱水處理時,纖維素III之晶體結 構佔整體結晶少於4 0%爲佳,以1 0至3 5%更佳。纖 維素III之含量少於1 〇 %時無法得到令人滿意之預期防縮 性,而纖維素III含量爲4 0 %或更高時,手感會變硬。 其次,對於具有因液態氨處理而產生纖維素III結晶結 構之纖維素纖維紡織品在伸展或非伸展狀態下進行熱水處 理或苛性鹼處理,因此使纖維素纖維紡織品中至少一部分 纖維素III晶體結構轉變成纖維素I或II晶體結構。 更特別的是,根據本發明使用下列程序之一可以將至 少部分纖維素III晶體結構轉換成纖維素I或II晶體結構: 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 476833 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(6 ) (a )首先經由液態氨處理將原有纖維素之纖維素I晶體 結構轉換成纖維素III,並經由熱水處理轉換回纖維素I ; (b )首先經由液態氨處理將再生纖維素之纖維素II晶體 結構轉換成纖維素III,並經由熱水處理將其轉換回纖維素 II ; ( c )首先以絲光作用將原有纖維之纖維素I結晶結 構轉換成纖維素II,之後經由液態氨處理將其轉變成纖維 素III,並以熱水處理將其轉換回纖維素II ;以及(d )首 先經由液態氨處理將原有纖維素I或II晶體結構轉換成纖 維素III,並經苛性鹼處理將其轉換回纖維素II。 在纖維素晶體結構轉變期間,所有纖維素結晶並不一 定進行轉變。最終產物之晶體狀態係其已經過之步驟所產 生之纖維素晶體狀態混合物。 熱水處理係將纖維素纖維紡織品浸在溫度爲1 0 0至 1 5 0 °C,以1 1 0至1 4 0 °C爲佳之熱水中進行。更特 別的·是使用可在高壓下進行熱水處理之裝置。例如,以高 壓液態流動染色機器,高壓槳葉式染色機器,高壓捲染機 ,高壓轉筒染色機器或高壓經軸染色機器進行熱水處理。 此等熱水處理時間依熱水溫度等而定,不過其一般約 爲1 0分鐘至大約5小時,以2 0分鐘至大約4小時爲佳 。適當時間係於1 0 0 °C時至少2小時,1 1 0 °C時至少 1小時,1 2 0°C時至少4 0分鐘,1 3 0°C時至少2 0 分鐘。476833 A7 B7 V. Description of the invention (1) Background of the invention Field of the invention The present invention relates to a method for preventing shrinkage of cellulose fiber textiles. More specifically, the method for treating cellulose fiber textiles makes the textile completely shrink-proof without loss of basic strength. Therefore, it minimizes the shrinkage after washing and minimizes the hardening after repeated washing. Previous techniques So far, cellulose fiber textiles have been widely used as clothing materials because they have the advantages of regulating moisture absorption, good feel and easy handling. However, such cellulose fiber textiles will shrink after washing and have problems of hardening after repeated washing. Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back before filling this page). The reasons for shrinkage after cleaning are related to two phenomena. One of the phenomena is that the knitted fabric is deformed due to various factors during the manufacturing and processing. In more detail, · The woven knitted fabric is tossed and twisted in a free state without external force at the time of washing, and it is easy to return to the original stable state, thereby causing contraction. This shrinkage can be prevented by mechanical methods, such as mechanical pre-shrinking. This method uses a rubber belt or a felt layer type pre-shrinking machine to continuously and continuously shrink the fiber to reduce the possibility of shrinking the fiber and impart shrinkage resistance. However, this method cannot sufficiently reduce the possibility of shrinking of thick fiber cloth or hard final fiber. Another phenomenon is that the shrinkage of a woven knitted fabric is the result of individual fibers absorbing and swelling with water to increase their cross-sectional area. This contraction is caused by the absorption of water. After the fiber is dried to remove moisture, the fiber tissue cannot return to its original size before swelling. The paper size is in accordance with the Chinese National Standard (CNS) A4 (210X 297 mm) 476833 A7 B7. 5. The original description of the invention description (2). The fibers remain contracted. SUMMARY OF THE INVENTION The present invention proposes a method for treating cellulose fiber textiles, which is sufficiently shrink-proof without substantial loss of strength, so that its shrinkage after washing is minimized, and the hardening of the hand after repeated washing is minimized. . The present inventors have discovered that by treating cellulose fiber textiles with liquid ammonia, and then treating the fiber textiles with hot water or caustic under stretched or non-stretched conditions, the cellulose fiber textiles can be fully shrink-proof, so that they are useful for cleaning Shrinkage resistance is minimized after the washing, and the hardening of the hand after repeated washing is minimized. It is done without substantial loss of strength. Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs (please read the notes on the back before filling this page). In more detail, when pre-impregnated cellulose fiber textiles with liquid ammonia, the liquid ammonia not only penetrates into the amorphous phase area, Penetration into the crystalline region of cellulose breaks the hydrogen bonds, thereby causing the fiber to swell as a whole. Thereafter, heat treatment is performed to evaporate the liquid ammonia where the hydrogen bonds were newly formed, and at least a part of the crystalline region generates a cellulose III crystal structure. The crystals are fixed in a swollen state. This result reduces crystallinity. When such fibers are finally treated with resin, the anti-wrinkle and anti-shrink properties are improved, and the strength is slightly lost. This fact is known in the art. In contrast, after liquid ammonia treatment, by treating cellulose fiber textiles with hot water or caustic alkali, the crystal structure of cellulose III is restored to the crystal structure of cellulose I or II. During the process, hot water or caustic alkali penetrates during this process. , Still maintain the state of swelling. The fibrous structure is then fixed to swell and relax. Therefore, the influence of water swelling and stretching and relaxation due to cleaning is minimized or the paper size applies the Chinese National Standard (CNS) A4 specification (210X 297 mm) 476833 A7 B7 5. The invention description (3) is eliminated. Anti-shrink processing is done in this way. Subsequent resin treatment on this cellulose fiber textile treated in this way can give it improved wrinkle or shrink resistance compared to before resin treatment, without substantial loss of strength. In more detail, the resin treatment of the cellulose fiber textiles of the prior art has an increase in the amount of resin added and an improvement in wrinkle resistance or shrinkage resistance, but the tensile strength tends to decrease at the same time. When the tensile strength decreases, the hydrogen bonds can be stabilized by cross-linking the cellulose fibers, thereby improving the anti-wrinkle and anti-shrink properties. This is because of the possibility of regional brittle fracture due to the introduction of cross-linking. These situations contradict each other. A compromise must be found to improve shrinkage resistance and avoid loss of strength. Since cellulose fibers have a multiphase structure including crystalline and amorphous phase portions or skin and internal portions, it is necessary to uniformly distribute the crosslinked groups to avoid loss of strength. Printed by the Consumer Affairs Cooperation Card of the Central Bureau of the Ministry of Economic Affairs of the Ministry of Economic Affairs (please read the notes on the back before filling out this page) This need is met below. When fibers that have been sufficiently swelled with liquid ammonia treatment are treated with hot water or caustic under stretched or non-stretched conditions, some changes in the fiber structure in the swollen state are made to improve the accessibility of the fibers so that The ideal crystal structure of the connection points is distributed as uniformly as possible to achieve the improvement of the wrinkle resistance or the shrinkage resistance. When the fibers in this state are further treated with a resin, a small amount of resin is sufficient to improve the shrinkage prevention properties. The smaller the amount of resin added, the less the strength loss. In this way, a reasonable compromise between the above conflicting needs can be achieved. The anti-shrinkage treatment method of the present invention is beneficial to the production of sufficiently shrink-resistant cellulose fiber textiles without causing substantial loss of strength, minimizing the shrinkage effect after washing and minimizing the hardening of the touch after repeated washing. In particular, this paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) 476833 A7 B7 V. Description of the invention (4) It can make cotton, linen, and rayon thin and low-strength textiles with improved anti-shrinkage Or wrinkle resistance to maintain practically acceptable strength. Therefore, the present invention provides a method for preventing shrinkage of cellulose fibers, which comprises treating the fiber textile with liquid ammonia, and then treating the fiber textile with hot water or caustic under stretched or non-stretched, and selectively treating the fiber with resin. Knot fabric. Detailed description of the invention The shrink-proof treatment method of the present invention comprises step (1), treating cellulose fiber textiles with liquid ammonia, and step (2) treating the fiber textiles with hot water or caustic under stretched or non-stretched conditions. i Printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back before filling this page) The cellulose fiber textiles that can be treated by the method of the present invention are composed of cellulose fibers including natural fibers and regenerated cellulose fibers For example, cotton, hemp, coriander, polynosic, copper ammonium fiber, and high-strength regenerated cellulose fiber (for example, those commercially available under the trademark Tene 1). These natural fibers and regenerated cellulose fibers can be in the form of mixed fiber materials, which are prepared by blending their dagger fibers, such as synthetic fibers, with polyesters and polyamides. The mixed fiber material must have a relatively large amount of cellulose fibers, and a cellulose fiber content of at least 50% by weight is more preferable. The alkali treatment can be performed on fibers that are insoluble in the alkali solution used. Cellulose fiber textiles that can be used herein include woven fibers, knitwear, and nonwoven fibers. If necessary, the textile can be pretreated, such as scorching, desizing, scouring, bleaching and mercerizing. The textile can also be dyed or printed. This paper size applies Chinese National Standard (CNS) A4 (210 X 297 mm) 476833 A7 B7 V. Description of Invention (5) First, the cellulose fiber textile is treated with liquid ammonia, which is maintained at atmospheric pressure-3 3 Pre-preg the textile with liquid ammonia at ° C or lower. The significance of this prepreg includes immersion in liquid ammonia, spraying liquid ammonia, and coating liquid ammonia. The prepreg time can be appropriately selected in the range of about 5 to 40 seconds. 0 Liquid ammonia is most commonly used to trigger the conversion of cellulose I or II in cellulose fiber textiles into cellulose II. However, lower alkyl groups can be used if necessary. Amines such as methylamine and ethylamine. At the end of the process, the ammonia is removed from the cellulose fiber textile treated with liquid ammonia by heating. This liquid ammonia treatment causes the crystal structure of cellulose I or II to be converted into cellulose III crystals in proportion to the prepreg time. When the prepreg time is 5 seconds, the cellulose III crystal structure accounts for about 10% of the overall crystal, about 15% at 8 seconds, 25% at 12 seconds, and about 35% at 18 seconds. And about 40% at 20 seconds or more. Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back before filling this page) • When the liquid ammonia is treated with hot water, the crystal structure of cellulose III accounts for less than 40% of the total crystallization. Better, preferably from 10 to 3 5%. When the content of cellulose III is less than 10%, satisfactory anti-shrinkage properties cannot be obtained, and when the content of cellulose III is 40% or more, the feel becomes hard. Secondly, the cellulose fiber textiles with cellulose III crystal structure produced by liquid ammonia treatment are subjected to hot water treatment or caustic treatment in the stretched or non-stretched state, so that at least a part of the cellulose III crystal structure in the cellulose fiber textile is made. Conversion to cellulose I or II crystal structure. More specifically, according to the present invention, at least part of the cellulose III crystal structure can be converted into cellulose I or II crystal structure using one of the following procedures: This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) 476833 Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs A7 B7 V. Description of the invention (6) (a) First, the original cellulose cellulose I crystal structure is converted to cellulose III by liquid ammonia treatment, and converted by hot water treatment Cellulose I; (b) First, the cellulose II crystal structure of regenerated cellulose is converted to cellulose III by liquid ammonia treatment, and it is converted back to cellulose II by hot water treatment; (c) first, The cellulose I crystal structure of the original fiber is converted to cellulose II, which is then converted to cellulose III by liquid ammonia treatment, and then converted back to cellulose II by hot water treatment; and (d) first by liquid ammonia treatment The original cellulose I or II crystal structure is converted into cellulose III, and it is converted back to cellulose II by caustic treatment. During the transformation of cellulose crystal structure, all cellulose crystals are not necessarily transformed. The crystalline state of the final product is a mixture of cellulose crystalline states resulting from the steps that it has undergone. Hot water treatment is performed by immersing cellulose fiber textiles in hot water at a temperature of 100 to 150 ° C, preferably at 110 to 140 ° C. More specifically, a device capable of performing hot water treatment under high pressure is used. For example, high-pressure liquid flow dyeing machines, high-pressure paddle dyeing machines, high-pressure pad dyeing machines, high-pressure drum dyeing machines, or high-pressure beam dyeing machines perform hot water treatment. These hot water treatment times depend on the temperature of the hot water, etc., but are generally about 10 minutes to about 5 hours, and preferably 20 minutes to about 4 hours. The appropriate time is at least 2 hours at 100 ° C, at least 1 hour at 110 ° C, at least 40 minutes at 120 ° C, and at least 20 minutes at 130 ° C.

該熱水處理造成至少部分,以至少2 5 %爲佳,至少 4 0 %纖維紡織品中之纖維素III晶體結構轉變回纖維素I 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) (請先閱讀背面之注意事項再填寫本頁) •裝· 、v" 476833 A7 B7 五、發明説明(7 ) 或II晶體結構。更特別的是,當該晶體結構因液態氨處理 而由纖維素I轉換成纖維素III時,其可藉熱水處理變回纖 維素I。當其由纖維素II開始時,該晶體結構可藉熱水處 理變回纖維素II。纖維素III變成纖維素I或II之轉換百分 比可依{(熱水處理前整體結晶中纖維素III之含量百分比 )-熱水處理後整體結晶中之纖維素III含量百分比)} / (熱水處理前整體結晶中纖維素III之含量百分比)X 1 0 0 〇 熱水處理係該紡織品於伸展或非伸展狀態下進行。熱 水處理係視紡織品種類和應用而使用高壓液態流動染色機 器,高壓轉筒染色機器或高壓槳葉式染色機器,並使該紡 織品維持非伸展狀態下進行。或者,使用高壓經軸染色機 器或高壓捲染機器,使該紡織品維持平坦狀態(伸展狀態 下)下進行。 經濟部中央標準局員工消費合作社印製 •當熱水處理在紡織品非伸展狀態下使用高壓液態流動 染色機器,高壓轉筒染色機器或者高壓葉槳式染色機器進 行時,紡織材料中之應力會鬆弛,結果改善防縮性。其它 優點係因爲熱水處理的固定效果可改善濕/乾防皺性,可 使其具有垂感及質感,並且改變其外觀。 另一方面,當熱水處理係在紡織品於平坦狀態(或於 伸展狀態)下,使用高壓經軸染色機器或高壓捲染機器進 行時,其優點係可使該紡織品不產生皺折或不規則狀,而 且織邊不經滾壓,其係因在熱水處理期間該紡織品維持平 坦之故。故可以進行大規模處理。 10 (請先閱讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(21〇Χ297公釐) 476833 A7 B7 五、發明説明(8 ) 熱水處理可應用於染色及印花紡織品。在此種情況下 ,可在熱水處理之前對該纖維素纖維紡織品染色或印花。 熱水處理不需使用鹼性或酸性酸類,諸如苛性蘇打和乙醯 酸,該經染色或印花紡織品之熱水處理不會降低色彩或染 料之牢固性。因爲對於樹脂最終處理之需求消除,會產生 輕微强度下降。若無樹脂最終處理,零伸展下之纖維素纖 維紡織品熱水處理在鬆弛狀態下,製得防縮天然纖維素纖 維紡織品,其於清洗1 0回合之後經紗清洗收縮百分比係 棉織品高達1 · 5 %,麻織品高達2 . 0 %,以及苧麻織 品高達2 . 0 %。亦可製得防縮天然纖維素纖維針織品, 諸如單集圈棉針織物,其於清洗1 0回合後之經紗/緯紗 清洗收縮之總百分比高達1 5 . 0 %。另外可製得防縮性 再生纖維素纖維機織品,其於清洗1 0回合後經紗清洗收 縮百分比係嫘縈短纖維紡織品高達3 . 0 %,嫘縈長絲, 嫘榮·短纖維紡織品高達3 · 5%,而銅銨嫘縈纖維高達 2 . 0 %。必須注意的是收縮百分比係依J I S L — 2 1 7 1 〇 3方法清洗紡織品,隨後滾筒式烘乾而測定 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 0 另一程序中,上述液態氨處理之後,對該纖維素纖維 進行苛性鹼處理。此苛性鹼處理係對於伸展或非伸展狀態 下之纖維素纖維紡織品進行。 苛性鹼係使用眾所周知之裝置諸如絲光處理機器進行 。更特別的是,以苛性鹼水溶液預浸該纖維素纖維紡織品 ,如此將至少部分纖維素III晶體結構轉變成纖維素II晶體 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 11 476833 A7 ___B7_____ 五、發明説明(9 ) 結構。本文使用之苛性鹼一般爲氫氧化鈉(NaOH)或 氫氧化鉀(K 0 Η ),以氫氧化鈉爲佳。若情況需要,可 使用其它鹼性化學藥品。 通常該紡織品係以苛性鹼濃度0 . 1至4 0重量%之 苛性鹼水溶液在一 1 0 °C至1 5 0 °C溫度下處理大約2 0 秒至大約2 4秒。 在9 0 °C或以下之溫度使用苛性鹼水溶液進行苛性鹼 處理,下文稱爲低溫鹼處理,該溶液之苛性鹼濃度以10 至4 0%爲佳,1 5至4 0%更佳,1 5至3 0重量%最 佳。適用之處理溫度係一 1 0 °C至9 0 °C,1 0 °C至4 0 °C更佳。苛性鹼處理之時間不需特定,其因該苛性鹼溶液 之濃度和溫度而定。該處理時間一般約爲2 0秒至2 4小 時。 經濟部中央標準局員工消費合作社印製 (請先閲讀背面之注意事項再填寫本頁) 在高於9 0°C溫度下使用苛性鹼水溶液進行苛性鹼處 理,·下文中稱之爲高溫鹼處理,該溶液之苛性鹼濃度爲 〇 · 1至1 0%爲較,0 · 2至5重量%更佳。適當的處 理溫度爲9 0 °C至1 5 0 °C,以1 0 0 °C至1 5 0 °C更佳 ,1 1 0 °C至1 4 0 °C最佳。苛性鹼處理時間不需特別限 定,其依苛性鹼溶液之濃度和溫度而定。該處理時間一般 大約1分鐘至大約5小時,以1 0分鐘至5小時爲佳, 2 0分鐘至3小時更佳。 假如該苛性鹼濃度過低,該苛性鹼處理會變得無效。 假如該苛性鹼濃度變得太高,並無進一步改善,而且造成 隨後去除苛性鹼中和步驟需要更多時間和成本缺點。 本紙張尺度適用中國國家標準((:灿)八4規格(210/297公釐)_12_ " 476833 A7 B7 五、發明説明(10 ) 上述低溫和高溫鹼處理可在該纖維素纖維紡織品伸展 或非伸展狀態下進行。 該纖維素纖維紡織品之苛性鹼水溶液用量至少佔該欲 預浸之纖維素纖維紡織品5 0重量%。可使用浸軋機將苛 性鹼水溶液施用於纖維素纖維紡織品。可使用印花技藝中 所用之印花機器將苛性鹼水溶液塗於纖維素纖維紡織品選 定部分。 若情況需要,可以在使用苛性鹼水溶液之前對該纖維 素纖維紡織品染色或印花。 該苛性鹼處理係在該纖維素纖維伸展或非伸展下進行 。依該紡織品種類及應用而定,可使用液態流動染色機器 ,轉筒染色機器或葉漿式染色機器使該紡織品在非伸展狀 態下進行苛性鹼處理。或者,該紡織品在伸展狀態下時, 使用絲光處理機器,高壓經軸染色機器或高壓捲染機器進 行該苛性鹼處理。非伸展狀態下之苛性鹼具有熱水處理可 達成的相同優點。 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 伸展狀態下使用絲光機器進行之苛性鹼處理具有使該 紡織品具有無皺折或不規則情形,而且織邊不經滾軋,其 係因爲該苛性鹼處理期間紡織品保持平坦之故,而且可以 大規模處理。此實例中,處理時間一般爲2 0至8 0秒。 然後以酸處理經此苛性鹼處理之纖維素纖維紡織品’ 其用以中和鹼,並以水清洗之。此處使用之酸包括無機酸 ,諸如硫酸和氫氯酸與有機酸,諸如醋酸和甲酸。 上述有關液態氨處理與其後之熱水處理或苛性鹼處理 本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐)_ ^ - 476833 A7 ____B7_ 五、發明説明(η ) 之方法具有許多優點。因爲根本無法使用藉甲醛爲代表之 樹脂,故無殘留在紡織品中之甲醛。可以製得强度無實質 損失之充分防縮纖維素纖維紡織品。本發明有利於使厚織 品或硬質最終織品具有良好防縮性’以及改良光澤及染色 密度。 根據本發明防縮方法,視情況需要在上述液態氨處理 及其後伸展或非伸展狀態下進行熱水或苛性鹼處理之後, 可以進行樹脂完工。 本處使用之樹脂可爲與纖維素羥基反應形成交聯之化 合物任何一者,例如醛類,諸如甲醛,乙二醛及戊二醛, 環氧化合物,諸如二縮水甘油醚,聚酸酸,諸如四丁烷羧 酸,以及纖維素反應羥甲基化合物,諸如二羥甲基脲,三 羥甲基三聚氰胺,二羥甲基乙烯脲及二羥甲基二羥基乙烯 脲。其中,纖維素反應N —羥甲基化合物最佳,因爲其具 有防皺或防縮性改良及紡織品强度損失之良好平衡。 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 此種樹脂之適當用量爲1至10重量%,尤其是2至 6重量%,其係以欲處理纖維素纖維紡織品爲基準計算之 固體。該樹脂少於1 %則樹脂完工效果較差,然而該樹脂 多於1 0 %會導致强度之實質損失。 根據本發明之樹脂,因爲防皺或防縮性改良之故,使 用蒸氣相使纖維素纖維紡織品與甲醛反應,其已知爲VP 反應。VP反應之細節可參考日本纖維素學會期刊,第2 卷,2 2頁。 在VP反應中,甲醛添加量最好爲0 . 1至3重量% 本紙張尺度適用中國國家標準(〇奶)八4規格(210'乂297公釐)_14_ 476833 A7 _B7_ 五、發明説明(I2 ) ,其係以纖維素纖維紡織品爲基準計算之固體。其係因爲 假若分子量小於N —羥甲基化合物之甲醛與N —羥甲基化 合物添加量相等,會造成過多交聯而使强度下降。甲醛少 於0 . 1 %會使樹脂完工效果較差,然而超過3 %甲醛會 使强度實質下降。 樹脂處理步驟中,可添加觸媒以增加樹脂與纖維素之 反應度,得到迅速樹脂處理。本文使用之觸媒可爲樹脂處 理慣用觸媒任何一者,例如氟硼化物,諸如氟硼化銨,氟 硼化鈉,氟硼化鉀和氟硼化鋅,中性金屬鹽觸媒,諸如氯 化鎂,硫酸鎂以及硝酸鎂,以及無機酸類,諸如磷酸,氫 氯酸,硫酸,亞硫酸,連二亞硫酸以及硼酸。若情況需要 ,該觸媒可與共觸媒併用,例如有機酸類,諸如檸檬酸, 酒石酸,蘋果酸以及順式丁烯二酸。 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 若情況需要,可於樹脂中添加輔助劑以確使該樹脂與 纖維.素反應平順。即,該輔助劑之功能係促進樹脂與纖維 素反應,充作反應溶劑使交聯反應均勻並潤脹該纖維。輔 助劑實例包括多羥醇類,諸如甘油,伸乙基乙二醇,聚伸 乙基乙二醇及聚伸丙基乙二醇;醚醇類,諸如伸乙基乙二 醇一乙醚,二伸乙基乙二醇醇一乙醚,伸乙基乙二醇醚, 二伸乙基乙二醇一甲醚及二伸乙基乙二醇一 丁醚;含氮溶 劑諸如二甲基甲醢胺,嗎啉,2 —吡喀烷酮,二甲基乙醯 胺及N —甲基吡咯烷酮;以及酯類,諸如醋酸乙酯,醋酸 異丙酯,醋酸丁酯,醋酸戊酯,醋酸伸乙基乙二醇一甲醚 酯,醋酸伸乙基乙二醇一乙醚酯及r .丁內酯。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) ΓΖ 1〇 476833 A7 B7 五、發明説明(13 ) 必須注意的是除上述化學藥品化,若情況需要,可於 樹脂中加入其它添加劑,例如調整手感之軟化劑及降低自 由甲醛濃度之甲醛清除劑。 可以任何需要之方法將樹脂塗在纖維素纖維紡織品上 。可在已知方法中做選擇,諸如塡塞乾燥和甲醛蒸汽相( V P )反應。塡塞乾燥法包括將織物浸於樹脂之液態製備 物中,以壓水率5 0至1 2 0 %壓擠該織品,並於大約 7 0至1 0 0 °C環境溫度下乾燥該織品以去除水。在低於 7 0°C環境溫度下需要乾燥時間較長,而高於1 0 〇°C環 境溫度下,可能會發生樹脂移動,導致樹脂分佈不均勻。 之後,該纖維素與樹脂一起於1 2 0至1 7 0°C (特別是 1 3 0至16 0°C)溫度下熱處理1至1 5分鐘,特別是 2至1 0分鐘,造成交聯作用。該熱處理時間依樹脂種類 及用量,解媒種類及用量等而定。熱處理溫度低於1 2 0 °C會使反應變慢,而熱處理溫度高於1 7 0 °C會使織品黃 化0 經濟部中央標準局員工消費合作社印m (請先閱讀背面之注意事項再填寫本頁) 該V P反應方法使用甲醛作爲樹脂,並將蒸汽相甲醛 塗覆於織品上。在一般過程中,可藉由塡塞乾燥法等事先 將軟化劑,聚伸乙基乙二醇等塗覆在織品。該紡織品置於 密閉容器中,於該容器導入甲醛和酸性氣體,諸如二氧化 硫,如此使該織品吸收該氣體化合物。然後加熱該織品使 之交聯。黏合之甲醛用量大約爲該織品0·1至3重量% ,溫度爲2 0至1 6 0°C,處理時間大約1至6 0分鐘。 防縮處理之後接著樹脂處理之具體化實例中,與慣用 本紙張尺度適用中國國家標準(CNS )A4規格( 210X297公釐)_ 16 . '~' 476833 經濟部中央標準局員工消費合作社印裂 A7 B7 五、發明説明(14 ) 樹脂處理相比較其樹脂添加量可減少相當多,如此減少織 品强度下降。製得更爲防皺或防縮之纖維素纖維織品。即 使在單薄,强度低織品實例,諸如棉,麻和嫘縈中,可使 其具有高度防皺或防縮性,並維持實際可接受强度。 本發明防縮處理後,該纖維素纖維織品可進行最終處 理,諸如拉幅及手感調整。 實施例 本發明下列實施例係供參考而非限制。 實施例1 5 0支單紗之平織1 0 0 %棉織品(經紗密度1 4 8 支紗/英寸,緯紗密度8 0支紗/英寸)慣常漂白以液態 氨處理1 0秒鐘並加熱蒸發該氨。然後利用高壓液體流動 染色機在非伸展下以1 3 0 °C熱水處理2小時,隨後脫水 ,乾燥並拉幅。 奮施例2 在6 0支單紗平織1 0 〇 %麻織品(經紗密度6 0支 紗/英寸,緯紗密度5 2支紗/英寸)進行實施例1之處 理。 y施例3 對6 0支之單紗平織1 Q 〇 %芋麻織品(經紗密度 本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐)-Η _ (請先閱讀背面之注意事項再填寫本頁) Γ 476833 A7 B7 五、發明説明(l5 ) 5 2支紗/英寸,緯紗密度5 6支紗/英寸)進行實施例 1之處理。 窗施例4 以針織機器(圓筒半徑3 0英寸而針密度爲1 8針/ 英寸)針織。4 0支之二股棉紗,製得原單集圈針織品, 對其進行實施例1之處理。 對照賨例丄_ 重複實施例1之程序,但是省略液態氨處理。 對照實例2二 重複實施例2之程序,但是省略液態氨處理。 對照·實例 重複實施例3之程序,但是省略液態氨處理。 經濟部中央標準局員工消費合作社印製 (請先閲讀背面之注意事項再填寫本頁) 對照實例 重複實施例4程序,但是省略液態氨處理。 對實施例1至4與對照實例1至4之機織和針織品進 行清洗試驗(J I S L - 2 1 7 1 0 3方法),其包 括清洗1回合或清洗1 0回合,隨後以滾筒乾燥。測量該 機織纖維緯紗收縮率。對於針織品而言,測量緯紗和經紗 收縮率總和。結果如表1所示。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) ~ " _ itt _ 476833 A7 B7 五、發明説明(16 ) 經濟部中央標準局員工消費合作社印製 棉針織品 〇 ο CO (Ν1 〇 LO οα 1 1 1 CD 03 τ-Η 〇 LO τ-Η 1 1 1 τ^τ rft 宁麻 CO ω ο 卜 r—Η ◦ CO 〇=> <=> ο CO Μ 呀 CD Τ-Η 1—Η 05 呀 CNI 卜 l—H 05 CO 呀 髏. <ΝΙ ω ο Ο CO CO <=> c=> ο CNI ω 寸 ο 1—1 〇〇 1—Η LO ◦ τ-Η 1—Η CO ι-Η ω ο 卜 r-H 〇 〇 Ο ο Ξ 卜 <=> Τ-Η 1-Η LO 〇 <ΝΙ 卜 i-H 卜 卜 清洗1回合 _ 清洗10回合 處理前 處理後 滌 變^ I—I :囉 3 ^ 籮忉 ΓΤΤ 1 ^ TQ 11 糴 鍵讲 纖維素Π 含量(%) 。ti褂驾一一者邻鎞«+§轺劫毖#邻^騷_蜡煺菡画}龌伞蟈鎰《笊骢騣伞者 €昍赵,唣·鎰迄φΒίι編刦劃骓某麵癱ifX cig昍运筚纖煺鐦 < 曰惡Π二條_ <nsl褂驩荽燊骢惡燊鍵 (請先閱讀背面之注意事項再填寫本頁) ·裝· 、訂 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 476833 A7 B7 五、發明説明(W ) 眚施例1 對於3 0支單紗之平織短紗1 0 0 %嫘縈織品(經紗 密度6 8支紗/英寸,緯紗密度6 0支紗/英寸)以液態 氨進行漂白,處理1 〇秒鐘,並加熱蒸發該氨。利用高壓 液體流動染色機器,在非伸展狀態下以1 3 0 °C熱水處理 2小時,隨後脫水,乾燥並拉幅。 實施例_ _止· 對於以1 2 0旦嫘縈長絲作爲經紗(經紗密度1 2 0 /英寸)及密度3 0單紗嫘縈短纖維(緯紗密度6 0 /英 寸)平織之經紗嫘縈長纖維織品進行實施例5之處理° 實施例7 對於以7 5旦銅銨嫘縈長纖維作爲經紗(經紗密度 1 4. 4 /英寸)及1 2 0旦銅銨嫘縈長纖維作爲緯紗(緯 紗密度8 7 /英寸)之平織銅銨1 0 0 %嫘縈織品進行實 施例5之處理。 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 對照實例5 重複實施例5程序,但是省略液態氨處理。 對照實例6 重複實施例6程序,但是省略液態氨處理。 本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐)_ _ 476833 A7 B7 五、發明説明(18 ) 對照實例7 重複實施例7程序,但是省略液態氨處理。 對實施例5至7與對照實例5至7之機織品進行清洗 試驗(JIS L— 217 103方法),其包括清洗 1回合或清洗1 0回合,隨後以滾筒乾燥。測量該機織品 及其緯紗收縮率。結果如表2所示。 (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 本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐)_ η - 476833 A7 B7 五、發明説明(19 ) 經濟部中央標準局員工消費合作社印製 m m m 卜 ο LO CO LO ① 卜 ο Τ-Η LO τ—Η m m ^ 鏃駿鷀 駿X CO Ο ο CO <ΝΙ ο LO (Μ CO ω LO <ΝΙ Ο CO ‘1111 繫 蘩 m ng m m m m LO Ο οο LO CO 卜 LO 呀 ι-Η CD CNI 回 <π 回 cz> 1-H 荽- (請先閱讀背面之注意事項再填寫本頁) ·裝·The hot water treatment caused at least partly, at least 25%, preferably at least 40% of the cellulose III crystal structure in the fiber textiles to be converted back to cellulose I. This paper size applies to Chinese National Standard (CNS) A4 specifications (210X 297 mm) (%) (Please read the precautions on the back before filling out this page) • Equipment, v " 476833 A7 B7 5. Description of the invention (7) or II crystal structure. More specifically, when the crystal structure is converted from cellulose I to cellulose III by liquid ammonia treatment, it can be changed back to cellulose I by hot water treatment. When it starts with cellulose II, the crystal structure can be changed back to cellulose II by hot water treatment. The conversion percentage of cellulose III to cellulose I or II can be based on {(percentage of cellulose III in the whole crystal before hot water treatment) -percent of cellulose III in the whole crystal after hot water treatment} / (hot water The percentage of cellulose III in the overall crystal before the treatment) X 1 0 0 0 Hot water treatment is performed in the stretched or non-stretched state of the textile. Hot water treatment is performed using a high-pressure liquid flow dyeing machine, a high-pressure drum dyeing machine, or a high-pressure paddle dyeing machine depending on the type and application of the textile, and maintaining the textile in a non-stretched state. Alternatively, use a high-pressure warp beam dyeing machine or high-pressure jig dyeing machine to keep the textile flat (stretched). Printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs • When hot water treatment is performed using a high-pressure liquid flow dyeing machine, a high-pressure drum dyeing machine, or a high-pressure paddle-type dyeing machine when the textile is not stretched, the stress in the textile material will relax The result is improved shrinkage resistance. Other advantages are that the fixing effect of hot water treatment can improve wet / dry wrinkle resistance, give it a drooping and texture, and change its appearance. On the other hand, when the hot water treatment is performed in a flat state (or in an extended state) using a high-pressure warp beam dyeing machine or a high-pressure jig dyeing machine, the advantage is that the textile does not wrinkle or irregularly. And the selvedge is not rolled because the textile remains flat during hot water treatment. Therefore, it can be processed on a large scale. 10 (Please read the precautions on the back before filling this page) This paper size is applicable to the Chinese National Standard (CNS) A4 specification (21 × 297 mm) 476833 A7 B7 5. Description of the invention (8) Hot water treatment can be used for dyeing And printed textiles. In this case, the cellulose fiber textile can be dyed or printed before hot water treatment. Hot water treatment does not require the use of alkaline or acidic acids, such as caustic soda and acetic acid. The hot water treatment of dyed or printed textiles does not reduce the color or the fastness of the dye. Because the need for final resin treatment is eliminated, there is a slight decrease in strength. If there is no resin final treatment, the cellulose fiber textiles under zero stretching are treated with hot water in a relaxed state to produce shrink-proof natural cellulose fiber textiles. After washing for 10 rounds, the warp washing shrinkage percentage is as high as 1.5% for cotton fabrics. Up to 2.0% of linen and up to 2.0% of ramie. Shrinkproof natural cellulose fiber knits, such as single-ply cotton knits, can also be made, and the total percentage of warp / weft cleaning after washing for 10 rounds is as high as 15.0%. In addition, shrink-proof regenerated cellulose fiber woven fabrics can be prepared. After washing for 10 rounds, the warp yarn cleaning shrinkage percentage is up to 3.0% for short-fiber textiles, and up to 3 for long-fiber, 嫘 rong · short-fiber textiles. 5%, and copper ammonium rhenium fiber up to 2.0%. It must be noted that the shrinkage percentage is printed in accordance with JISL-2 1 7 1 〇3 method, followed by tumble drying and printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back before filling this page) 0 In another procedure, after the above-mentioned liquid ammonia treatment, the cellulose fiber is subjected to a caustic treatment. This caustic treatment is performed on cellulose fiber textiles in a stretched or non-stretched state. Caustic is carried out using well-known equipment such as mercerizing machines. More specifically, the cellulose fiber textile is pre-impregnated with an aqueous caustic solution, so that at least part of the cellulose III crystal structure is transformed into cellulose II crystals. The paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 11 476833 A7 ___B7_____ 5. Description of the invention (9) Structure. The caustic used herein is generally sodium hydroxide (NaOH) or potassium hydroxide (K 0 Η), preferably sodium hydroxide. If necessary, other alkaline chemicals can be used. Generally, the textile is treated with an aqueous caustic solution having a caustic concentration of 0.1 to 40% by weight at a temperature of 10 ° C to 150 ° C for about 20 seconds to about 24 seconds. Caustic treatment using a caustic aqueous solution at a temperature of 90 ° C or below, hereinafter referred to as low-temperature caustic treatment, the caustic concentration of the solution is preferably 10 to 40%, more preferably 15 to 40%, 1 5 to 30% by weight is optimal. The applicable processing temperature is 10 ° C to 90 ° C, preferably 10 ° C to 40 ° C. The time of caustic treatment need not be specified, it depends on the concentration and temperature of the caustic solution. This processing time is generally about 20 seconds to 24 hours. Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs (please read the precautions on the back before filling this page). Use caustic aqueous solution for caustic treatment at a temperature higher than 90 ° C. The caustic concentration of the solution is from 0.1 to 10%, more preferably from 0.2 to 5% by weight. The appropriate processing temperature is 90 ° C to 150 ° C, more preferably 100 ° C to 150 ° C, and the best is 110 ° C to 140 ° C. The caustic treatment time is not particularly limited, and it depends on the concentration and temperature of the caustic solution. The treatment time is generally about 1 minute to about 5 hours, preferably 10 minutes to 5 hours, and more preferably 20 minutes to 3 hours. If the caustic concentration is too low, the caustic treatment becomes ineffective. If the caustic concentration becomes too high, there is no further improvement, and the subsequent caustic neutralization step would require more time and cost disadvantages. This paper size applies to Chinese national standard ((: Can) 8 4 specifications (210/297 mm) _12_ " 476833 A7 B7 V. Description of the invention (10) The above low temperature and high temperature alkali treatment can be stretched on the cellulose fiber textile or It is carried out in a non-stretched state. The amount of caustic aqueous solution of the cellulose fiber textile accounts for at least 50% by weight of the cellulose fiber textile to be pre-impregnated. The caustic aqueous solution can be applied to the cellulose fiber textile using a padding mill. Printing can be used The printing machine used in the art applies an aqueous caustic solution to selected portions of the cellulose fiber textile. If necessary, the cellulose fiber textile can be dyed or printed before using the aqueous caustic solution. The caustic treatment is applied to the cellulose fiber Stretching or non-stretching. Depending on the type and application of the textile, a liquid flow dyeing machine, a drum dyeing machine or a leaf pulp dyeing machine can be used to cause the textile to be caustic treated in a non-stretched state. In the stretched state, use a mercerizing machine, a high-pressure beam dyeing machine or This caustic treatment is performed by a high-pressure jig dyeing machine. Caustic in non-stretched state has the same advantages as hot water treatment. Printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back before filling this page) The caustic treatment using a mercerizing machine in the stretched state has the effect that the textile has no wrinkles or irregularities, and the selvedge is not rolled, because the textile remains flat during the caustic treatment, and can be used on a large scale Treatment. In this example, the treatment time is generally 20 to 80 seconds. The caustic-treated cellulose fiber textile is then treated with an acid, which is used to neutralize the alkali and wash it with water. The acid used here Including inorganic acids, such as sulfuric acid and hydrochloric acid, and organic acids, such as acetic acid and formic acid. The above-mentioned liquid ammonia treatment and subsequent hot water treatment or caustic treatment are applicable to this paper. Chinese national standard (CNS) A4 specification (210X297 mm) ) _ ^-476833 A7 ____B7_ 5. The method of the invention description (η) has many advantages. It is impossible to use formaldehyde as a representative at all. Resin, so there is no formaldehyde remaining in textiles. It is possible to produce fully shrinkable cellulose fiber textiles without substantial loss of strength. The present invention is conducive to making thick fabrics or hard final fabrics have good shrinkage resistance 'and improve gloss and dyeing density. According to According to the shrinkage prevention method of the present invention, after the above-mentioned liquid ammonia treatment and hot water or caustic alkali treatment in the stretched or non-stretched state are required, the resin can be completed. The resin used here can react with cellulose hydroxyl groups to form a cross Any one of the compounds, such as aldehydes, such as formaldehyde, glyoxal and glutaraldehyde, epoxy compounds, such as diglycidyl ether, polyacids, such as tetrabutanecarboxylic acid, and cellulose methylol Compounds such as dimethylol urea, trimethylol melamine, dimethylol ethylene urea and dimethylol dihydroxy ethylene urea. Among them, cellulose reacts with N-methylol compounds, because it has a good balance of improving wrinkle or shrink resistance and loss of textile strength. Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs (please read the notes on the back before filling this page) The appropriate amount of this resin is 1 to 10% by weight, especially 2 to 6% by weight. Plain fiber textiles are solids calculated on a benchmark basis. If the resin is less than 1%, the resin finishing effect is poor. However, more than 10% of the resin will cause a substantial loss of strength. The resin according to the present invention uses a vapor phase to react cellulose fiber textiles with formaldehyde, which is known as a VP reaction, because of improvement in wrinkle resistance or shrinkage resistance. For details of the VP reaction, please refer to the Journal of the Japan Cellulose Society, Vol. 2, p. 22. In the VP reaction, the amount of formaldehyde added is preferably 0.1 to 3% by weight. The paper size is applicable to the Chinese national standard (〇 奶) 8 4 specifications (210 '乂 297 mm) _14_ 476833 A7 _B7_ V. Description of the invention (I2 ), Which is a solid calculated on the basis of cellulose fiber textiles. The reason is that if the molecular weight of formaldehyde and N-methylol compound is smaller than that of N-methylol compound, it will cause excessive cross-linking and decrease the strength. Formaldehyde less than 0.1% will result in poor resin finishes, while more than 3% formaldehyde will substantially reduce strength. In the resin treatment step, a catalyst may be added to increase the reactivity between the resin and cellulose, resulting in rapid resin treatment. The catalyst used herein can be any of the conventional resin treatment catalysts, such as fluoroborides, such as ammonium fluoboride, sodium fluoroboride, potassium fluoroboride, and zinc fluoroboride, neutral metal salt catalysts, such as Magnesium chloride, magnesium sulfate and magnesium nitrate, as well as inorganic acids such as phosphoric acid, hydrochloric acid, sulfuric acid, sulfurous acid, dithionite and boric acid. If necessary, the catalyst can be used in combination with co-catalysts, such as organic acids such as citric acid, tartaric acid, malic acid, and cis-butenedioic acid. Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs (please read the precautions on the back before filling this page). If necessary, you can add an auxiliary to the resin to ensure that the resin and the fiber react smoothly. That is, the function of the auxiliary agent is to promote the reaction between the resin and cellulose, and act as a reaction solvent to make the crosslinking reaction uniform and swell the fiber. Examples of adjuvants include polyhydric alcohols, such as glycerol, ethylene glycol, polyethylene glycol, and polyethylene glycol; ether alcohols, such as ethylene glycol monoethyl ether, two Diethyl glycol glycol monoethyl ether, diethyl glycol glycol ether, diethylene glycol monomethyl ether and diethylene glycol monobutyl ether; nitrogen-containing solvents such as dimethylformamide , Morpholine, 2-pyrrolidone, dimethylacetamide and N-methylpyrrolidone; and esters such as ethyl acetate, isopropyl acetate, butyl acetate, pentyl acetate, ethyl acetate Ethylene glycol monomethyl ether ester, ethylene glycol acetate monoethyl ether and r. Butyrolactone. This paper size is applicable to Chinese National Standard (CNS) A4 specification (210X297 mm) ΓZ 1〇476833 A7 B7 V. Description of the invention (13) It must be noted that in addition to the above-mentioned chemicals, if necessary, other resins can be added to the resin. Additives, such as softeners to adjust hand feel and formaldehyde scavengers to reduce free formaldehyde concentration. The resin can be applied to cellulosic fiber textiles in any desired way. Choices can be made in known methods, such as plug drying and formaldehyde vapor phase (VP) reactions. The plug drying method involves immersing a fabric in a resinous liquid preparation, squeezing the fabric at a water pressure of 50 to 120%, and drying the fabric at an ambient temperature of about 70 to 100 ° C to Remove water. Drying takes longer at ambient temperatures below 70 ° C, and resin migration may occur at ambient temperatures above 100 ° C, resulting in uneven resin distribution. Thereafter, the cellulose is heat-treated together with the resin at a temperature of 120 to 170 ° C (especially 130 to 160 ° C) for 1 to 15 minutes, especially 2 to 10 minutes, causing crosslinking. effect. The heat treatment time depends on the type and amount of the resin, and the type and amount of the dissolving medium. Heat treatment temperature below 120 ° C will slow down the reaction, while heat treatment temperature above 170 ° C will yellow the fabric. 0 Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back first) (Fill in this page) This VP reaction method uses formaldehyde as the resin and coats the fabric with vapor phase formaldehyde. In the general process, softening agents, polyethylene glycol, etc. may be applied to the fabric in advance by a plug drying method or the like. The textile is placed in a closed container, and formaldehyde and an acid gas such as sulfur dioxide are introduced into the container, so that the fabric absorbs the gaseous compound. The fabric is then heated to crosslink it. The amount of formaldehyde to be bonded is about 0.1 to 3% by weight of the fabric, the temperature is 20 to 160 ° C, and the processing time is about 1 to 60 minutes. In the concrete example of anti-shrinking treatment followed by resin treatment, the Chinese paper standard (CNS) A4 specification (210X297 mm) is applied to the paper size commonly used. _ 16. '~' 476833 Employees' Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs print A7 B7 V. Description of the invention (14) Compared with resin treatment, the amount of resin added can be reduced considerably, thus reducing the strength of the fabric. A more crease-resistant or shrink-resistant cellulose fiber fabric is produced. Even in thin, low-strength fabric examples, such as cotton, linen, and linen, it can be highly wrinkle-proof or shrink-proof, while maintaining practically acceptable strength. After the shrink-proof treatment of the present invention, the cellulose fiber fabric can be subjected to final treatments such as tentering and hand feel adjustment. Examples The following examples of the present invention are for reference and not limitation. Example 150 Plain weaving of 100 single yarns of 100% cotton fabric (warp density of 148 yarns / inch, weft density of 80 yarns / inch) is conventionally bleached with liquid ammonia for 10 seconds and heated to evaporate the ammonia . Then use a high-pressure liquid flow dyeing machine to treat with non-stretching hot water at 130 ° C for 2 hours, then dehydrate, dry and tenter. Example 2 The treatment of Example 1 was performed on 60 single-thread plain weave 100% linen fabrics (warp density of 60 counts / inch and weft density of 52 counts / inch). y Example 3 For single-thread plain weaving of 60 counts, 1 Q 〇% taro linen (density of warp yarn, the paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm)-_ _ (Please read the precautions on the back first (Fill in this page again) Γ 476833 A7 B7 V. Description of the invention (l5) 5 2 yarns / inch, weft density 56 yarns / inch). Window Example 4 was knitted using a knitting machine (cylinder radius of 30 inches and needle density of 18 stitches / inch). Forty counts of two cotton yarns were used to obtain the original single tuck knitwear, which was processed in Example 1. Comparative Example _ The procedure of Example 1 was repeated, but the liquid ammonia treatment was omitted. Comparative Example 2 The procedure of Example 2 was repeated, but the liquid ammonia treatment was omitted. Comparative Example The procedure of Example 3 was repeated, but the liquid ammonia treatment was omitted. Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back before filling this page) Comparative Example The procedure of Example 4 was repeated, but the liquid ammonia treatment was omitted. The woven and knitted fabrics of Examples 1 to 4 and Comparative Examples 1 to 4 were subjected to a washing test (J I S L-2 1 7 1 0 3 method), which consisted of washing for 1 round or 10 rounds, followed by tumble drying. The weft yarn shrinkage was measured. For knitwear, measure the total shrinkage of weft and warp yarns. The results are shown in Table 1. This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) ~ " _ itt _ 476833 A7 B7 V. Description of the invention (16) Cotton knitwear printed by employees' cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs. Ν1 〇LO οα 1 1 1 CD 03 τ-Η 〇LO τ-Η 1 1 1 τ ^ τ rft 宁 麻 CO ω ο r—Η ◦ CO 〇 = > < = > ο CO Μ 呀 CD Τ -Η 1—Η 05 C CNI —l—H 05 CO 髅 骨. ≪ ΝΙ ω ο Ο CO CO < = > c = > ο CNI ω inch ο 1-1 〇〇1—Η LO ◦ τ -Η 1—Η CO ι-Η ω ο r rH 〇〇〇 ο Ξ & < = > Τ-Η 1-Η LO 〇 < ΝΙ イ i ー wash 1 round _ wash 10 rounds before processing Polyester ^ I—I: 啰 3 ^ 箩 忉 ΓΤΤ 1 ^ TQ 11 籴 key to talk about cellulose Π content (%). Ti coat one by one 鎞 + + + 轺 邻 # ^^ 骚 _ 蜡 _ Painting} 龌 Umbrella 笊 骢 騣 "Umbrella 者 昍 Zhao, 唣 · 镒 Β φ ΒΒι edited and robbed a certain face paralysis ifX cig 昍 筚 筚 煺 鐦 煺 鐦 煺 鐦 lt ΠΠ 二条 _ & nsns骢 Evil Key (Please read the notes on the back before filling Page) · Packing · The size of the paper is applicable to the Chinese National Standard (CNS) A4 specification (210X 297 mm) 476833 A7 B7 V. Description of the invention (W) 眚 Example 1 For 30 single yarn plain weave spun yarns 1 A fabric of 0 0% (warp density of 68 yarns / inch, weft density of 60 yarns / inch) was bleached with liquid ammonia, treated for 10 seconds, and heated to evaporate the ammonia. Using a high-pressure liquid flow dyeing machine, In a non-stretched state, it is treated with hot water at 130 ° C for 2 hours, and then dewatered, dried, and tentered. Example _ 止 · For a yarn of 1 20 denier filaments as a warp (warp density 1 2 0 / Inch) and density of 30 single yarn 嫘 萦 short fibers (weft density of 60 / inch) plain woven warp 进行 long fiber fabrics were treated in Example 5 ° Example 7 For 7.5 denier copper ammonium 嫘 萦 long fibers The warp yarn (warp yarn density 14.4 / inch) and 120 denier copper ammonium rayon long fibers were used as the weft yarn (weft yarn density 87 / inch) to produce the plain weave copper ammonium 100% rayon fabric. Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs (Please read the notes on the back first Then fill page) Comparative Example 5 Example 5 The procedure was repeated, but omitting the liquid ammonia treatment. Comparative Example 6 The procedure of Example 6 was repeated, but the liquid ammonia treatment was omitted. This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) _ 476833 A7 B7 V. Description of the invention (18) Comparative Example 7 The procedure of Example 7 was repeated, but the liquid ammonia treatment was omitted. The woven fabrics of Examples 5 to 7 and Comparative Examples 5 to 7 were subjected to a washing test (JIS L-217 103 method), which included washing for 1 round or 10 rounds, followed by drum drying. Measure the shrinkage of the woven fabric and its weft. The results are shown in Table 2. (Please read the notes on the back before filling this page) The paper size printed by the Employees' Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs applies the Chinese National Standard (CNS) A4 specification (210X297 mm) _ η-476833 A7 B7 (19) Printed mmm by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs ο LO CO LO ① ο Τ-Η LO τ—Η mm ^ 镞 骏 鹚 骏 X CO Ο ο CO < ΝΙ ο LO (Μ CO ω LO < ΝΙ Ο CO '1111 蘩 m ng mmmm LO Ο οο LO CO LO 呀 ι-Η CD CNI back < π back cz > 1-H 荽-(Please read the notes on the back before filling this page) · Loading ·

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本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐)_ U 476833 A7 B7 五、發明説明(2〇 ) 實施例a_ 將7支之1 〇 〇 %棉粗斜紋機織紡織品(經紗密度 6 5支紗/英寸,緯紗密度4 3支紗/英寸)以液態氨在 一 3 4 °C下預浸1 0秒,加熱蒸發該氨,慣常退漿,然後 利用高壓經軸染色機在平坦狀態下於1 3 0 °C熱水處理2 小時,隨後拉幅。 實施例 在8支棉/嫘縈(4 0 / 6 0 )混紡粗斜紋布1 0 0 %機織紡織品(經紗密度6 9支紗/英寸,緯紗密度4 3 支紗/英寸)上進行實施例8之處理。 實施例1 _0_ 在2 1支經紗(經紗密度1 1 5支紗/英寸)和1 〇 支緯·紗(緯紗密度5 4支紗/英寸)之天絲粗斜紋布 1 0 0%機織紡織品上進行實施例8之處理。 經濟部中央標準局員工消費合作社印裂 (請先閱讀背面之注意事項再填寫本頁) 對照實例 重複實施例8程序,但是省略熱水處理。 對照實例!_ 重複實施例9程序,但是省略熱水處理。 對昭奮例1 Q_ 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐)- 476833 A7 B7 五、發明説明(2i ) 重複實施例1 〇程序,但是省略熱水處理。 以下列試驗測量實施例8至1 0及對照實例8至1 0 之機織紡織品收縮率及抗張强度。結果示於表3。 依JIS L - 1 0 9 6 F — 2方法清洗該紡織品 丄,5及1 0回合,隨後滾筒乾燥。測量紡織品之經紗及 緯紗收縮率。 _强1 依J I S L - 1 0 9 6測量緯紗抗張强度。 (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費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公釐)-24 - 476833This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) _ U 476833 A7 B7 V. Description of the invention (20) Example a_ A 100% cotton denim woven textile of 7 (warp density 6 5 yarns / inch, weft density 4 3 yarns / inch) Pre-soaked with liquid ammonia at 34 ° C for 10 seconds, heated to evaporate the ammonia, customarily desizing, and then using a high-pressure warp beam dyeing machine in a flat state Treat with hot water at 130 ° C for 2 hours, and then stretch. EXAMPLES Example 8 was performed on 8 cotton / 棉 (40/60) blended denim 100% woven textiles (warp yarn density 69 yarns / inch, weft yarn density 4 3 yarns / inch) deal with. Example 1 __ performed on 21 warp yarns (warp yarn density 1 15 yarns / inch) and 10 weft yarns (weft yarn density 5 4 yarns / inch) Tencel denim 100% woven textiles The treatment of Example 8. Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back before filling this page) Comparative Example The procedure of Example 8 was repeated, but the hot water treatment was omitted. Comparative example! _ The procedure of Example 9 was repeated, but the hot water treatment was omitted. For Zhaofen Example 1 Q_ This paper size applies Chinese National Standard (CNS) A4 specifications (210X 297 mm)-476833 A7 B7 5. Description of the invention (2i) Repeat the procedure of Example 10, but omit the hot water treatment. The shrinkage and tensile strength of the woven textiles of Examples 8 to 10 and Comparative Examples 8 to 10 were measured by the following tests. The results are shown in Table 3. Wash the textile 丄 according to JIS L-10 9 6 F-2, rounds 5 and 10, and then tumble dry. Measure warp and weft shrinkage of textiles. _Strong 1 Measure the tensile strength of weft according to J I S L-1 0 9 6. (Please read the notes on the back before filling out this page) Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs This paper size applies to China National Standard (CNS) A4 (210x297 mm) -24-476833

A 經濟部中央標準局員工消費合作社印製 五、發明説明(22 ) LO CNI 〇 r-H 〇 Ο Ο 卜 LO g CO ③ CO r-H 卜· 〇〇 od 呀 c=> m 〇 <=> 卜 CM* r-H ω CO r-H 呀· LO 卜 CO ① m 1-Η 1 1-H 1 r-H 1 CO c<i g 象 Q CN1 ③ i-H r-H 觀 r-H <nJ 1—Η CNI t—H 卜 CO CD cn> ω 轤 ai 1 ο 1 O CD σί 卜 ο 呀 τ—i 観 CO οο od 卜 CO i—1 m r-H 1 r-H 1 t—H 1 o 〇〇 • S <Μ CO CO T-H T-H ai CM· 1—Η CO r-H CM CM 〇〇 Μ czJ 1 <=> 1 C5 1 CO 05 οο ① CM· 05 観 CO od φ 回 <π 回 I 回 o s Lw s m 激 (N 讲 ε ο m , "So m (請先閱讀背面之注意事項再填寫本頁) "口 Γ 本紙張尺度適用中國國家標準(〔灿)八4規格(210'乂297公釐)_ 476833 A7 B7 五、發明説明(23 ) 實施例1 1 對於8 0支二股紗平織之棉1 〇 G機織紡織品(經紗 密度,1 4 9支紗/英寸,緯紗密度6 2支紗/英寸)慣 常漂白,於一 3 4 °C以液態氨處理1 〇秒,並加熱蒸發該 氨。然後在伸展狀態下,以2 〇重量%苛性鹼於2 5 °C預 浸6 0秒,中和並以水清洗,隨後脫水,乾燥並拉幅。 對照實例1 1 重複實施例1 1程序,但是省略液態氨處理。 對照實例1 2 重複實施例1 1程序,但是省略苛性鹼處理。 如實施例8,測量實施例1 1與對照實例1 1及1 2 之收縮率及抗張强度。結果示於表4。 (請先閱讀背面之注意事項再填寫本頁) ·衣_A Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs. 5. Description of invention (22) LO CNI 〇rH 〇〇 〇 LO g CO ③ CO rH · 〇〇od Yeah c = > m 〇 < = > CM * rH ω CO rH Ye LO LO CO ① m 1-Η 1 1-H 1 rH 1 CO c < ig like Q CN1 ③ iH rH view rH < nJ 1—Η CNI t—H CO CO cn > ω 轳 ai 1 ο 1 O CD σί ο οτ—i 観 CO οο od CO i—1 m rH 1 rH 1 t—H 1 o 〇〇 • S < Μ CO CO TH TH ai CM · 1— Η CO rH CM CM 〇〇Μ czJ 1 < = > 1 C5 1 CO 05 οο ① CM · 05 観 CO od φ back < π back I back os Lw sm excitation (N speak ε ο m, " So m (Please read the precautions on the back before filling out this page) " 口 Γ This paper size is applicable to the Chinese national standard ([chan) 8 4 specifications (210 '乂 297 mm) _ 476833 A7 B7 V. Description of the invention (23 ) Example 1 1 For 80 two-ply yarn plain knitted cotton 1 〇 G Woven textiles (warp yarn density, 149 yarns / inch, weft yarn density: 62 yarns / inch) are conventionally bleached, treated with liquid ammonia at 34 ° C for 10 seconds, and heated to evaporate the ammonia. Then stretched In the state, pre-soak with 20% by weight caustic at 25 ° C for 60 seconds, neutralize and wash with water, then dehydrate, dry and tenter. Comparative Example 1 1 Repeat the procedure of Example 11 1 but omit the liquid Ammonia treatment. Comparative Example 12 The procedure of Example 11 was repeated, but the caustic treatment was omitted. As in Example 8, the shrinkage and tensile strength of Example 11 and Comparative Examples 11 and 12 were measured. The results are shown in the table. 4. (Please read the notes on the back before filling this page) · 衣 _

、1T 經濟部中央標準局員工消費合作社印製 本紙張尺度適用巾國國家標準(CNS)A4規格(21〇χ297公羡)_ % 476833 A7 B7 五、發明説明(24 ) 經濟部中央標準局員工消費合作社印製、 1T Printed by the Consumer Standards Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs. The paper size is applicable to National Standards (CNS) A4 (21 × 297). _% 476833 A7 B7 V. Description of the Invention (24) Staff of the Central Standards Bureau of the Ministry of Economics Printed by Consumer Cooperatives

(請先閱讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 27 - 476833 A7 B7 五、發明説明(25 ) 實施例1 2 對於4 0支二股紗單集圈(3 0英寸X 1 8隔距)之 棉1 〇 0%針織品進行慣用漂白及絲光處理,於一 3 4 °C 以液態氨預浸10秒,並加熱蒸發該氣。然後以16wt %苛性鹼於2 5 °C預浸5 0秒,中和並以水清洗,隨後脫 水,乾燥並拉幅。 實施例1 3 重複實施例1 2程序,但是省略該絲光處理。 對照實例1 3 重複實施例1 2程序,但是省略苛性鹼處理。 對照實例1 4 .重複實施例1 3步驟,但是省略苛性鹼處理。 如實施例8,測量實施例1 2與1 3及對照實例1 3 與1 4機織紡織品之清洗收縮率及依J I S L — 1 0 1 8慕藍方法測試其頂破强度。結果示於表5。 (請先閱讀背面之注意事項再填寫本頁) ·裝. 訂 經濟部中央標準局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(2川><297公釐)-28 - 476833(Please read the precautions on the back before filling in this page) This paper size applies Chinese National Standard (CNS) A4 specification (210X297mm) 27-476833 A7 B7 V. Description of the invention (25) Example 1 2 For 40 counts 100% knitwear of cotton with two single yarn loops (30 inches X 1 8 gauge) was subjected to conventional bleaching and mercerizing treatment, pre-soaked with liquid ammonia at 34 ° C for 10 seconds, and heated to evaporate the gas. It was then pre-soaked with 16 wt% caustic at 25 ° C for 50 seconds, neutralized and washed with water, followed by dehydration, drying and tentering. Example 1 3 The procedure of Example 12 was repeated, but this mercerizing treatment was omitted. Comparative Example 1 3 The procedure of Example 12 was repeated, but the caustic treatment was omitted. Comparative Example 1 4. The steps of Example 13 were repeated, but the caustic treatment was omitted. As in Example 8, the cleaning shrinkage of the woven textiles in Examples 12 and 13 and Comparative Examples 1 3 and 14 were measured, and their burst strength was tested in accordance with the J I S L — 1 0 1 8 Mulan method. The results are shown in Table 5. (Please read the precautions on the back before filling out this page.) · Binding. Order printed on the paper by the Consumer Standards Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs. Applicable to China National Standard (CNS) A4 (2 Sichuan > < 297 mm) -28-476833

7 B 經濟部中央標準局員工消費合作社印製 五、發明説明(26 )7 B Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs V. Invention Description (26)

ω 〇 m CD 卜 LO 〇〇 〇 卜 OO 〇 CD ⑦ CO <=> T-H CO τ-Η ω ο 轤 LO 卜 <=> 〇〇 〇〇 〇〇 r—H OD LO 〇〇 〇〇 〇〇 LO σ> CO ϊ—Η ω m CNI 卜 卜 LO 〇〇 i-H o T-H 象 m LO 1—Η CO CM CO <ΝΙ ίγ-Η 盤 〇〇 CO LO 卜 o oo LO cz> r—1 観 (NI LO CO LO 卜 LO fnT 回 τ-Η 回 LO 1±LL G5 i-H 躬 曰 o \ < bo m 讲 纏 /-N 镔 R (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 476833 A7 B7__ 五、發明説明(27 ) 下列實施例列舉高溫鹼處理。 實施例1 4一1 7 將4 0支單紗平織棉1 0 0 %紡織品(經紗密度 1 3 2支紗/英寸,緯紗密度7 1支紗/英寸)做慣用漂 白作用,於一 3 4 °C以液態氨預浸1 0秒,並加熱蒸發該 氨。然後在非伸展狀態下以濃度及溫度如表6所示之苛性 鹼溶液處理表6所示之時間,中和並以水清洗,隨後脫水 ,乾燥並拉幅。 如實施例1檢測實施例1 4至1 7之紡織品收縮性和 抗張强度。結果示於表6。 (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 本紙張尺度適用中國國家標準(CNS ) M規格(no'〆297公釐) 30 - 476833 明説 明 3發五經濟部中央標準局員工消費合作社印製 卜 T—Η ω U Λ <ΝΙ X Ο Ο ο CO 1—Η Q LO m r—1 <〇 1 CO <=> 1 ΟΟ ο 1 CO 03 観 CO CO r-H 05 ι—1 卜 CO 0〇 CO Τ-Η u X: Od X ο ο ο CO τ—Η c=> CO Τ—Η Ο ς〇 ο 1 寸 ο 1 〇 鍵 卜 τ-Η 卜 τ-Η r-H <ΝΙ CO οα 〇〇 LO r—1 Μ {-I Λ οα X ο ο ο CO τ-Η CD T—l m <ΝΙ Ο 1 LO ◦ 1 卜 ο 1 卜 LO 観 σ> 1-Η CNI CO <>α <=> 〇〇 〇〇 呀 τ-Η Λ C<J X! Ο Ο G5 CO τ-Η LO C=> Μ τ-Η Ο 1 CO o 1 05 <〇 1 G5 LO 寸 観 οο r-H r—H CM CO <>ί CO CO CD 蘧 m /-N 鹋 m m <π 回 τ-Η 回 LO φ 回 ο τ-Η H-h 'bO m 餵 m 缌 1 m ^ (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 476833 A7 B7 五、發明説明(29 ) 眚施例1 8 — 1 9&對照實例1 5 — 1 6 於一 3 4 °C以液態氨預浸棉1 0 0 %平織紡織品(經 紗:5 0支,密度1 4 8支紗/英寸,緯紗5 0支,密度 8 0支紗/英寸)2 0秒,加熱蒸發該氨,然後利用高壓 經軸染色機於平坦狀態下,以1 3 0 °C熱水處理之。 之後,依表7和8所示配方製備樹脂溶液,並利用塡 塞乾燥法對該紡織品進行樹脂處理。該樹脂處理包括以壓 漿率設爲6 0 %之軋液機塗用該樹脂溶液,於8 5 °C預乾 1 5分鐘,並於表7及8所示之條件下熱處理。測量如此 製得之實施例1 8與1 9紡織品之乾燥防皺性質與抗張强 度。結果示於表7與8。抗張强度與乾燥防皴性質之關係 如表1與2所示。必須注意的是依J I S L — 1 0 9 6 測量紡織品之抗張强度及乾燥防皺性質。 對照實例1 5與1 6與實施例1 8和1 9相同,但是 省略·熱水處理。 (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費合作社印製 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -32 - 476833 A7 B7 五、發明説明(30 ) 經濟部中央標準局員工消費合作社印製 CE15 壊 LO 1—Η οα r-H CO 140 CO CO ⑦ CNI 225 〇 1—Η οα t-H CO 140 CO CO LO <NI 248 LO i-H CM τ-Η CO 140 CO <M CO CNI 271 τ-Η οα r-H CO 140 CO ① o CM 290 E18 高壓經軸染色機 LO τ—Η CNI τ-Η CO 140 CO oo <NI 241 〇 i-H CM τ-Η CO 140 CO r—1 CO <NI 270 LO τ-Η CNI τ-Η CO 140 CO CNI <NI 287 τ-Η τ-Η CO 140 CO CO CO CNI 300 熱水處理 LNB20*1 氟硼化鋅μ ΡΕ-140*5 PEG200*6 溫度(°C ) 時間(分) 抗張強度 (kgf ) 乾燥防皺性1 質(。) 熱處理 紐織品性 質 (請先閲讀背面之注意事項再填寫本頁)ω 〇m CD and LO 〇〇〇〇OO 〇 〇CD ⑦ CO < = > TH CO τ-Η ω ο 轳 LO and < == > 〇〇〇〇〇〇〇r-H OD LO 〇〇〇〇〇 〇〇LO σ > CO ϊ—Η ω m CNI BU LO 〇〇iH o TH image m LO 1—Η CO CM CO < ΝΙ ίγ-Η disc 〇COCO 卜 o oo LO cz > r-1 (NI LO CO LO LOLO fnT back τ-Η back to LO 1 ± LL G5 iH bow o \ < bo m talk about / -N 镔 R (Please read the precautions on the back before filling this page) The paper size Applicable to China National Standard (CNS) A4 specification (210X297 mm) 476833 A7 B7__ V. Description of the invention (27) The following examples enumerate the high-temperature alkali treatment. Example 1 4 1 17 4 40 single yarn plain woven cotton 1 0 0 % Textiles (with a warp density of 13 2 yarns / inch and a weft density of 71 yarns / inch) for conventional bleaching. Pre-soak with liquid ammonia at 34 ° C for 10 seconds, and then heat and evaporate the ammonia. In a non-stretched state, treat the time shown in Table 6 with a caustic solution with the concentration and temperature shown in Table 6, neutralize and wash with water. Then dewater, dry, and tenter. The shrinkage and tensile strength of the textiles of Examples 14 to 17 were tested as in Example 1. The results are shown in Table 6. (Please read the precautions on the back before filling this page) Ministry of Economy Printed by the Central Bureau of Standards Consumer Cooperatives This paper is printed in accordance with the Chinese National Standard (CNS) M specification (no'〆297 mm) 30-476833 Note 3 issued by the Central Bureau of Standards of the Ministry of Economic Affairs Consumer Cooperatives printed T-Η ω U Λ < ΝΙ X Ο Ο ο CO 1—Η Q LO mr—1 < 〇1 CO < = > 1 ΟΟ ο 1 CO 03 観 CO CO rH 05 ι-1 1 CO 0〇CO Τ- Η u X: Od X ο ο ο CO τ—Η c = > CO Τ—Η Ο ς〇ο 1 inch ο 1 〇 bond τ-Η τ τ-Η rH < ΝΙ CO οα 〇〇LO r— 1 Μ {-I Λ οα X ο ο ο CO τ-Η CD T—lm < ΝΙ Ο 1 LO ◦ 1 Bu ο 1 Bu LO 観 σ > 1-Η CNI CO < > α < = > 〇〇〇〇 呀 τ-Η Λ C < JX! Ο Ο G5 CO τ-Η LO C = > Μ τ-Η Ο 1 CO o 1 05 < 〇1 G5 LO 観 οο rH r—H CM CO < > ί CO CO CD 蘧 m / -N 鹋 mm < π Back to τ-Η Back to LO φ Back to τ-Η Hh 'bO m Feed m 缌 1 m ^ (Please read the precautions on the back before filling this page) This paper size applies Chinese National Standard (CNS) A4 specifications (210X 297 Mm) 476833 A7 B7 V. Description of the invention (29) 眚 Example 1 8 — 1 9 & Comparative Example 1 5 — 1 6 Pre-impregnated cotton with liquid ammonia at 1 34 ° C 100% plain woven textile (warp yarn: 50 counts, density 1 4 8 counts / inch, weft 50 counts, density 80 counts / inch) 20 seconds, heat and evaporate the ammonia, and then use a high-pressure warp beam dyeing machine in a flat state to 1 3 0 ° C hot water treatment. After that, a resin solution was prepared according to the formulations shown in Tables 7 and 8, and the textile was subjected to resin treatment using a plug drying method. The resin treatment includes coating the resin solution with a rolling mill set at 60%, and pre-drying at 85 ° C for 15 minutes, and heat treating under the conditions shown in Tables 7 and 8. The thus-made textiles of Examples 18 and 19 were measured for their dry wrinkle resistance and tensile strength. The results are shown in Tables 7 and 8. The relationship between tensile strength and dry moth-proof properties is shown in Tables 1 and 2. It must be noted that the tensile strength and dry wrinkle resistance of textiles are measured in accordance with J I S L — 1 0 9 6. Comparative Examples 15 and 16 are the same as those of Examples 18 and 19, but omit the hot water treatment. (Please read the notes on the back before filling out this page) The paper size printed by the Central Consumers Bureau of the Ministry of Economic Affairs's Consumer Cooperatives applies the Chinese National Standard (CNS) A4 specification (210X297 mm) -32-476833 A7 B7 V. Description of the invention (30) CE15 printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 壊 LO 1—Η οα rH CO 140 CO CO ⑦ CNI 225 〇1—Η οα tH CO 140 CO CO LO < NI 248 LO iH CM τ-Η CO 140 CO < M CO CNI 271 τ-Η οα rH CO 140 CO ① o CM 290 E18 High pressure beam dyeing machine LO τ—Η CNI τ-Η CO 140 CO oo < NI 241 〇iH CM τ-Η CO 140 CO r—1 CO < NI 270 LO τ-Η CNI τ-Η CO 140 CO CNI < NI 287 τ-Η τ-Η CO 140 CO CO CO CNI 300 Hot water treatment LNB20 * 1 Zinc fluoroborate μ PE -140 * 5 PEG200 * 6 Temperature (° C) Time (minutes) Tensile strength (kgf) Dry wrinkle resistance 1 quality (.) Heat treated button fabric properties (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規格( 210X297公釐)_幻 476833 A7 B7 五、發明説明(31 ) 經濟部中央標準局員工消費合作社印製This paper size applies to China National Standard (CNS) A4 (210X297 mm) _Magic 476833 A7 B7 V. Description of Invention (31) Printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs

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¾ 0Abfl03 G <D •rH Oei •i—I •rH ◦ 寸 m mpn. 画 m ECQ MM m- 鉍矻.3 ·}! SIS Η3Ιβοϊ 曰 9qol<Ds-l—l9N« •3.3 IcdoiluCDqοOUIO-H*l—(ans AJ-Hsnpui JSIm9q°.5JUI ^H3 Isis-B 二 j〇k ® C«^: a -O 漱 CD嫠f蘅Θ5 键I盤齡ο与,fr齡® 蠊驩 次_勸:I 1 I X CD · · 遯#AJ ·. ◦—〇 C^:^ s -H cd cz? 0 .tTT-T . *»-H ^ (NJ 曰·—〇 —Λ 3 <υω 〇 CZ) s Ou (M CO 寸 LO CO 兴兴兴兴兴 (請先閲讀背面之注意事項再填寫本頁) _裝. 訂 本紙張尺度適用中國國家標準(CNS)A4規格(210X297公釐)_ ^ 476833 A7 B7 五、發明説明(32 ) 必須注意的是,該樹脂溶液係於表7與8所示之化學 配方中添加水至1 0 Omp製得。 賨施例2 0與對照實例1 7 將實施例1 8所使用之棉1 0 0 %平織紡織品於 一 3 4 °C下以液態氨預浸1 0秒,加熱蒸發該氨,利用高 壓液體流動染色機器在非伸展狀態下,以1 3 0 °C熱水處 理1小時,最後使用表9所示之樹脂配方及條件做樹脂完 工。如實施例1 8試驗經此處理之實施例2 0紡織品。結 果示於表9與圖3。 對照實例1 7與實施例2 0相同,但是省略熱水處理 (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費合作社印製 35 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 476833 五、發明説明(33 ) 經濟部中央標準局員工消費合作社印製 CE17 壊 LO r-H οα 1—Η CO 140 CO ο 250 G5 τ-Η οα r-H CO 140 CO (ΝΙ ς=> CNI 253 LO τ—( (ΝΙ r-H CO 140 CO <〇 ο <ΝΙ 262 τ-Η <ΝΙ t—Η CO 140 CO οο αο τ—Η 274 Ε20 高壓液體流動染色機 . . LO τ-Η (ΝΙ τ-Η CO 140 CD 1-Η CNI 252 <=> 03 1—Η CO 140 CO ΟΟ CNI CNI 267 LO ι-Η 03 τ-Η CO 140 CO Ο CNI 03 271 τ—Η (ΝΙ ι—Η CO 140 CO 寸 r-H <ΝΙ 281 熱水處理 LNB20*1 氟硼化鋅 * ΡΕ-140*5 PEG200*6 溫度(°C ) 時間(分) 抗張強度 (kgf) 乾燥防皴性 質Γ ) 樹脂配方 (g/ 1 0 0ml ) 熱處理 紡織品性 質 (請先閲讀背面之注意事項再填寫本頁)¾ 0Abfl03 G < D • rH Oei • i—I • rH ◦ inch m mpn. Picture m ECQ MM m-bismuth 矻 .3 ·}! SIS Η3Ιβοϊ 9qol < Ds-l—l9N «• 3.3 IcdoiluCDqοOUIO-H * l— (ans AJ-Hsnpui JSIm9q ° .5JUI ^ H3 Isis-B II jOK ® C «^: a -O CD 嫠 f 蘅 Θ5 key I disc ageο, fr age ® 蠊 欢 次 _ advise: I 1 IX CD · · 遁 #AJ ·. ◦—〇C ^: ^ s -H cd cz? 0 .tTT-T. * »-H ^ (NJ name · —〇—Λ 3 < υω 〇CZ) s Ou (M CO inch LO CO Xing Xing Xing Xing Xing (Please read the notes on the back before filling in this page) _Package. The size of the paper is applicable to China National Standard (CNS) A4 (210X297 mm) _ ^ 476833 A7 B7 V. Description of the invention (32) It must be noted that the resin solution is prepared by adding water to 10 Omp in the chemical formula shown in Tables 7 and 8. 賨 例 2 0 and Comparative Example 17 will be implemented Example 18 Cotton 100% plain woven textiles were pre-soaked with liquid ammonia for 10 seconds at 34 ° C. The ammonia was heated to evaporate, and the high-pressure liquid flow dyeing machine was used in a non-stretched state at 1 3 0. ° C hot water treatment for 1 hour, and finally use the resin composition shown in Table 9 The conditions and conditions are to complete the resin. As in Example 18, the textile of Example 20 treated with this test is tested. The results are shown in Table 9 and Figure 3. Comparative Example 17 is the same as Example 20, but the hot water treatment is omitted (please (Please read the notes on the back before filling in this page) Printed by the Central Consumers Bureau of the Ministry of Economic Affairs Employee Cooperatives 35-This paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 476833 V. Description of the invention (33) Ministry of Economy Printed by the Consumer Standards Cooperative of the Central Bureau of Standards CE17 壊 LO rH οα 1—Η CO 140 CO ο 250 G5 τ-Η οα rH CO 140 CO (ΝΙ ς = > CNI 253 LO τ— ((ΝΙ rH CO 140 CO < 〇ο < ΝΙ 262 τ-Η < ΝΙ t—Η CO 140 CO οο αο τ—Η 274 Ε20 High-pressure liquid flow dyeing machine: LO τ-Η (ΝΙ τ-Η CO 140 CD 1-Η CNI 252 < = > 03 1-ΗCO 140 CO ΟΟ CNI CNI 267 LO ι-Η 03 τ-ΗCO 140 CO Ο CNI 03 271 τ-Η (ΝΙιι-ΗCO 140 CO inch rH < ΝΙ 281 hot water treatment LNB20 * 1 Zinc fluoboride * PE-140 * 5 PEG200 * 6 Temperature (° C) Time (minutes) Tensile strength (kgf) Dry Dryness and anti-corrosion properties Γ) Resin formula (g / 100ml) Heat treatment Textile properties (Please read the precautions on the back before filling this page)

、1T 本紙張尺度適用中國國家標準(CNS ) Α4規格(210 X 297公釐) 36 476833 A7 B7 五、發明説明(34 ) 實施例2 1與對照實例1 8 將實施例1 8所使用之棉1 0 0%平織紡織品於 一 3 4 °C下以液態氨預浸2 0秒,加熱蒸發該氨,利用慣 用絲光處理機於伸展狀態下,於2 5 °C以2 0 w t %苛性 蘇打處理6 0秒,最後使用表1 0所示之樹脂配方和條件 做樹脂完工。對實施例2 1如此處理之紡織品作同實施例 1 8之物理性質試驗。結果示於表1 0和圖4。 對照實例1 8與實施例2 1相同,但是省略苛性蘇打 處理。 (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費合作社印製 37 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 476833 A7 B7 五、發明説明(35 ) 經濟部中央標準局員工消費合作社印製 CE18 壊 LO t-H r-H CO 140 CO CD ① οα 225 ◦ τ-Η <N1 t—H CO 140 CO CO LO CM 248 LO r-H οα r-H CO 140 CO oa CO CNI 271 Τ-Η CNI τ-Η CO 140 CO CD '<Z> 1 290 Ε21 絲光處理機 LO τ-Ή <NI 1—H CO 140 CD oo CNI 252 C=> l-H Od τ-Η CO 140 CO OO 卜 C<I 267 LO r-H CNI r-H CO 140 CO c=> 卜 1 271 τ-Η (Nl r-H CO 140 CO CO 281丨 熱水處理 LNB20* 1 氟硼化鋅 * Pc-ι PE-140*5 PEG200*6 溫度(°C ) 時間(分) 抗張強度 (kgf ) 乾燥防皺性 質(。) 樹脂配方 (g/ 10 0ml ) 熱處理 紡織品性1 質 | (請先閲讀背面之注意事項再填寫本頁) -·裝·、 1T This paper size applies the Chinese National Standard (CNS) A4 specification (210 X 297 mm) 36 476833 A7 B7 V. Description of the invention (34) Example 2 1 and Comparative Example 1 8 The cotton used in Example 1 8 100% plain woven textiles were pre-soaked with liquid ammonia at 34 ° C for 20 seconds, and the ammonia was heated to evaporate. Using a conventional mercerizing machine in the stretched state, treated with 20 wt% caustic soda at 25 ° C. 60 seconds, and finally use the resin formulation and conditions shown in Table 10 to complete the resin. The textile thus treated in Example 21 was subjected to the same physical property test as in Example 18. The results are shown in Table 10 and Fig. 4. Comparative Example 18 was the same as Example 21 except that the caustic soda treatment was omitted. (Please read the notes on the back before filling out this page) Printed by the Central Consumers Bureau of the Ministry of Economic Affairs, Consumer Cooperatives 37-This paper size is applicable to the Chinese National Standard (CNS) A4 (210X 297 mm) 476833 A7 B7 V. Description of the invention (35) CE18 printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs 壊 LO tH rH CO 140 CO CD ① οα 225 ◦ τ-Η < N1 t—H CO 140 CO CO LO CM 248 LO rH οα rH CO 140 CO oa CO CNI 271 Τ-Η CNI τ-Η CO 140 CO CD '< Z > 1 290 Ε21 Mercerizing processor LO τ-Ή < NI 1-H CO 140 CD oo CNI 252 C = > lH Od τ-Η CO 140 CO OO C < I 267 LO rH CNI rH CO 140 CO c = > Pl 1 271 τ-Η (Nl rH CO 140 CO CO 281 丨 Hot water treatment LNB20 * 1 zinc fluoroboride * Pc-ι PE -140 * 5 PEG200 * 6 Temperature (° C) Time (minutes) Tensile strength (kgf) Dry anti-wrinkle properties (.) Resin formula (g / 10 0ml) Heat treated textile properties 1 quality | (Please read the note on the back first (Fill in this page again)-· Install ·

、1T 本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐)_货_ 476833 A7 B7 五、發明説明(36) 眚施f?l丨2 2及對照實例1 9 亞麻1 0 〇 %平織紡織品(經紗:大麻,6 0支,密 度6 0支紗/英寸,緯紗:大麻,6 0支,密度5 0支紗 /英寸)在一 3 4 °C下以液態氨預浸1 0秒,加熱蒸發該 氨,利用高壓液體流動染色機於非伸展狀態下以1 3 0 °C 熱水處理1小時,最後以表1 1所示之樹脂配方和條件做 樹脂完工。同實施例1 8,測量如此處理之實施例2 2紡 織品物理性質。結果示於表1 1和圖5。 對照實例1 9與實施例2 2相同,但是省略熱水處理 步驟。 (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 -39 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 476833 A7 B7 五、發明説明()37 經濟部中央標準局員工消費合作社印製 CE19 壊 1—H CO τ-Η CO 120 CO CNI CNI 206 CNI r-H <NI r-H CO 120 CO o i-H CNI 213 LO T-H <NI r-H CO 120 CO o CNI 213 〇〇 t—H CNI 1—H CO 120 CO oo c^> i-H 217 E22 高壓液體流動染色機 T-H CNI 1—H CO 120 CO CD <NI 204 οα r—H i-H CO 120 CO CNI CNI <NI 215 LO r-H <NI T—H CO 120 CO 1—H CNI 223丨 oo r-H <NI i-H CO 120 CO CNI CD CNI 2 2 7 1 熱水處理 LNB2(T 1 氟硼化鋅〜 PE-140*5 PEG200*6 溫度(°C ) 時間(分) 抗張強度 (kgf ) 乾燥防皺性 質(。) 枳c: 熱處理 紡織品性 質 (請先閱讀背面之注意事項再填寫本頁)、 1T This paper size is in accordance with Chinese National Standard (CNS) A4 (210X297mm) _Goods_ 476833 A7 B7 V. Description of the invention (36) 眚 施 f? L 丨 2 2 and Comparative Example 1 9 Flax 1 0 % Plain woven textiles (warp: hemp, 60 counts, density of 60 counts / inch, weft: hemp, 60 counts, density of 50 counts / inch) Pre-soaked with liquid ammonia at 34 ° C for 10 seconds The ammonia was heated to evaporate, and treated with hot water at 130 ° C for 1 hour in a non-stretched state using a high-pressure liquid flow dyeing machine. Finally, the resin was completed using the resin formula and conditions shown in Table 11. In the same manner as in Example 18, the physical properties of the woven fabric of Example 22 thus treated were measured. The results are shown in Table 11 and Fig. 5. Comparative Example 19 was the same as Example 22 except that the hot water treatment step was omitted. (Please read the notes on the back before filling out this page) Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs -39-This paper size applies to China National Standard (CNS) A4 (210X297 mm) 476833 A7 B7 V. Description of the invention () 37 Printed by the Consumer Cooperative of the Central Bureau of Standards, Ministry of Economic Affairs, CE19 壊 1—H CO τ-Η CO 120 CO CNI CNI 206 CNI rH < NI rH CO 120 CO o iH CNI 213 LO TH < NI rH CO 120 CO o CNI 213 〇〇t—H CNI 1—H CO 120 CO oo c ^ > iH 217 E22 High pressure liquid flow dyeing machine TH CNI 1—H CO 120 CO CD < NI 204 οα r—H iH CO 120 CO CNI CNI < NI 215 LO rH < NI T—H CO 120 CO 1—H CNI 223 丨 oo rH < NI iH CO 120 CO CNI CD CNI 2 2 7 1 Hot water treatment LNB2 (T 1 zinc fluoroborate ~ PE-140 * 5 PEG200 * 6 Temperature (° C) Time (minutes) Tensile strength (kgf) Dry wrinkle resistance (.) 枳 c: Heat treated textile properties (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規格(210X297公釐) -40 - 476833 A7 B7This paper size applies to China National Standard (CNS) A4 (210X297 mm) -40-476833 A7 B7

QO 五、發明説明() 眘施例2 3與對照實例2 0 嫘縈1 0 0 %平織紡織品(經紗:3 〇支,密度6 8 支紗/英寸,緯紗:3 0支,密度6 0支紗/英寸)於 一 3 4 °C下以液態氨預浸1 0秒,加熱蒸發該氨,利用高 壓液體流動染色機,於非伸展狀態下以1 3 0 °C熱水處理 之,最後使用表1 2所示之樹脂配方與條件做樹脂完工。 如實施例1 8,測量實施例2 3經此處理紡織品之物理性 質。結果如表1 2和圖6所示。 對照實例2 0與實施例2 3相同,但是省略熱水處理 (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費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐41 - 476833 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(39 ) CE20 壊 LO r—Η τ-Η CO 120 O οα CM CO 184 ◦ r-H CNI t-H CO 120 o &lt;N1 oo cva 202 LO r—H οα r-H CO 120 o oo LO CNI 205 t-H r-H CO 120 o CO CO 207 E23 高壓液體流動染色機 m r-H (Μ τ-Η CO 120 ◦ CO r-H 230 CD t-H r-H CO 120 〇&gt; CO LO 227 LO r-H r-H CO 120 o CD &lt;Nl &lt;NI 249 r-H &lt;ΝΙ t-H CO 120 &lt;=&gt; CO T-H 248 熱水處理 LNB20*1 氟硼化鋅〜 PE-140*5 PEG200*6 溫度(°C ) 時間(分) 抗張強度 (kgf ) 乾燥防皺性 質(。) 樹脂配方 (g/ 100ml ) 熱處理 紡織品性 質 (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐 42 476833 A7 B7 五、發明説明() 實施例2 4及對照實例2 1 實施例1 8使用之1 0 0%棉平織紡織品於一 3 4 °C 下以液態氨預浸2 0秒,加熱蒸發該氨,利用高壓液體流 動染色機在非伸展狀態下,以1 3 0 °C熱水處理。最後之 樹脂處理,先藉由塡塞乾燥法在該紡織品上塗覆表1 3所 示之軟化劑和聚乙二醇,並於甲醛和二氧化硫氣體中,以 5 0至1 2 0°C進行交聯反應(VP反應)1 0分鐘。黏 合之甲醛量爲0.3重量%。 經此處理之實施例2 4紡織品係如實施例1 8試驗其 物理性質。結果如表1 3所示。 對照實例2 1與實施例2 4相同,但是省略熱水處理 (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 本紙張尺度適用中國國家標準(CNS ) M規格(UOX297公釐X “ 476833 A7 B7 五、發明説明(41 ) 表1 3 E24 CE21 熱水處理 高壓經軸 染色處理 m 處理劑 (g/100ml ) PE- 140_ 5 1 1 PEG200·5 3 3 紡織品性質 抗張强度 (kg f ) 43.0 40.3 乾燥防皺性質 (° ) 258 246 經濟部中央標準局員工消費合作社印製 (請先閲讀背面之注意事項再填寫本頁) 實施例2 5及對照實例2 2 將支數4 0二股紗單集圈(3 0英寸XI 8隔距)棉 1 〇 0 %針織品依慣用方式漂白,於一 3 4 °C以液態氨預 浸2 0秒,加熱蒸發該氨,利用高壓液體流動染色機在非 伸展狀態下以1 3 0 °C熱水處理1小時,旋轉乾燥並加熱 本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐X 44 - 476833 A7 B7 五、發明説明(42 ) 車乞燥之。然後利用拉幅機進行樹脂處理。該處理之樹脂配 方和條件與實施例18相同。依JIS L-2 1 7 1 0 3方法試驗該紡織品清洗及滾筒乾燥後之收 縮率(經紗+緯紗),並依J I S L - 1 0 1 8幕藍方 法試驗其頂破强度。結果示於表1 4。 對照實例2 2與實施例2 5相同,但是該紡織品於非 伸展狀態下以6 0 °C溫水處理1小時代替熱水處理。 (請先閲讀背面之注意事項再填寫本頁) •I裝· 訂 經濟部中央標準局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格( 210X297公釐)l 45 - 476833 A7 B7 五、發明説明(43 ) 經濟部中央標準局員工消費合作社印製 20% 1_:_ CE22 呀 &lt;N1 CO CO 卜 T-H 1 E25 LO 03 寸 CO LO 15°/〇 CE22 CO 卜 卜 oo LO CNI E25 CO CO CD 卜 co 10% CE22 〇〇 CO T-H r-H 呀 CM T-H &lt;NI LO E25 〇〇 ς〇 卜 〇&gt; oo r-H LO LO CE22 LO 〇〇 OO LO t—H 寸 CO r-H CNI 卜 E25 CO CD t—1 CO Ί—Ι T-H LO 1—H r-H ◦ 卜 樹脂濃度 清洗1回合 清洗5回合 清洗10回合 頂破強度(kg/cm2 ) 經紗+緯紗 收縮率 (%) (請先閲讀背面之注意事項再填寫本頁)QO V. Explanation of the invention () Example 2 3 and Comparative Example 2 0 嫘 萦 100% Plain weaving textile (warp yarn: 30 counts, density 6 8 counts / inch, weft: 30 counts, density 60 counts Yarn / inch) pre-soaked with liquid ammonia for 10 seconds at 34 ° C, heated to evaporate the ammonia, treated with high-pressure liquid flow dyeing machine, and treated with 130 ° C hot water in a non-stretched state, and finally used The resin formulations and conditions shown in Table 12 are used to complete the resin. As in Example 18, the physical properties of the textile treated in Example 23 were measured. The results are shown in Table 12 and Figure 6. Comparative Example 20 is the same as Example 2 3, but the hot water treatment is omitted (please read the precautions on the back before filling this page) Printed on the paper by the Consumer Standards Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs, China National Standard (CNS) A4 Specifications (210X297mm 41-476833 Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs A7 B7 V. Description of the invention (39) CE20 壊 LO r—Η τ-Η CO 120 O οα CM CO 184 ◦ rH CNI tH CO 120 o &lt; N1 oo cva 202 LO r—H οα rH CO 120 o oo LO CNI 205 tH rH CO 120 o CO CO 207 E23 High-pressure liquid flow dyeing machine m rH (Μ τ-Η CO 120 ◦ CO rH 230 CD tH rH CO 120 〇 &gt; CO LO 227 LO rH rH CO 120 o CD &lt; Nl &lt; NI 249 rH &lt; ΝΙ tH CO 120 &lt; = &gt; CO TH 248 Hot water treatment LNB20 * 1 Zinc fluoroborate ~ PE-140 * 5 PEG200 * 6 Temperature (° C) Time (minutes) Tensile strength (kgf) Dry wrinkle resistance (.) Resin formula (g / 100ml) Heat treated textile properties (Please read the precautions on the back before filling this page) This paper size applies to China National Standard (CNS) A4 specifications (21 0X 297 mm 42 476833 A7 B7 V. Description of the invention () Example 2 4 and Comparative Example 2 1 Example 1 8 1 of 10 0% cotton plain woven textiles were pre-impregnated with liquid ammonia at 34 ° C 2 0 In seconds, the ammonia is heated to evaporate, and the high-pressure liquid flow dyeing machine is used in a non-stretched state to treat with hot water at 130 ° C. In the final resin treatment, the textile is first coated by the plug drying method. Shown as a softener and polyethylene glycol, and in a formaldehyde and sulfur dioxide gas, the crosslinking reaction (VP reaction) at 50 to 120 ° C for 10 minutes. The amount of formaldehyde bonded was 0.3% by weight. After this Example 2 of the treatment 4 The textile was tested for its physical properties as in Example 18. The results are shown in Table 13. Comparative Example 2 1 is the same as Example 2 4 but the hot water treatment is omitted (please read the precautions on the back first) (Fill in this page again) Printed by the Central Consumers Bureau of the Ministry of Economic Affairs, Consumer Cooperatives The paper size is applicable to Chinese National Standards (CNS) M specifications (UOX297 mm X "476833 A7 B7 V. Description of the invention (41) Table 1 3 E24 CE21 Hot water Treatment of high-pressure warp beam dyeing treatment m (g / 100ml ) PE- 140_ 5 1 1 PEG200 · 5 3 3 Textile properties Tensile strength (kg f) 43.0 40.3 Dry and wrinkle resistance (°) 258 246 Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs (Please read the precautions on the back first) (Fill in this page again) Example 25 and Comparative Example 2 2 Count the number of yarns of 40 two-ply yarn (30 inches XI 8 gauge) cotton 100% knitted fabrics bleached in the usual manner at a temperature of 34 ° C Pre-soak with liquid ammonia for 20 seconds, heat and evaporate the ammonia, use a high-pressure liquid flow dyeing machine in a non-stretched state with hot water at 130 ° C for 1 hour, spin dry and heat. CNS) A4 specification (210X297 mm X 44-476833 A7 B7) 5. Description of the invention (42) The car is dry. Then the resin is processed by a tenter. The resin formulation and conditions for this treatment were the same as in Example 18. The shrinkage rate of the textile after washing and tumble drying (warp + weft) was tested in accordance with JIS L-2 1 7 1 0 3 method, and its burst strength was tested in accordance with J I S L-108 1 method. The results are shown in Table 14. Comparative Example 22 was the same as Example 25, but the textile was treated with 60 ° C warm water for 1 hour in the non-stretched state instead of hot water treatment. (Please read the precautions on the back before filling out this page) • I pack and order the paper printed by the Central Consumers' Bureau of the Ministry of Economic Affairs, Consumer Cooperatives, and the paper size is applicable to China National Standard (CNS) A4 (210X297 mm) l 45-476833 A7 B7 V. Description of the invention (43) Printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 20% 1 _: _ CE22 Yeah <N1 CO CO TH 1 E25 LO 03 inch CO LO 15 ° / 〇CE22 CO oo oo LO CNI E25 CO CO CD CO 10% CE22 〇〇CO TH rH Yeah CM TH &lt; NI LO E25 〇〇ς〇 卜 〇 &gt; oo rH LO LO CE22 LO 〇OOOO t—H inch CO rH CNI BU E25 CO CD t—1 CO Ί—Ι TH LO 1—H rH ◦ Resin concentration cleaning 1 round cleaning 5 round cleaning 10 round burst strength (kg / cm2) Warp + weft shrinkage (%) (Please read the note on the back first (Fill in this page again)

本紙張又度適用中國國家標準(CNS ) A4規格(210X297公釐X 46 476833 A7 B7 五、發明説明(44 ) 實_施例2 6及對照管例2 λ 重複實施例2 5程序,但是利用慣用絲光處理機在液 態氨處理之前對於伸展狀態同實施例2 1之針織紡織品, 以1 6 w t %苛性蘇打於2 5 °C預浸5 0秒。以同實施例 2 5方式試驗該紡織品之清洗收縮率(經紗+緯紗)及其 頂破强度。結果如表1 5所示。 對照實例2 3與實施例2 6相同,但是在非伸展狀態 下以6 0 °C清洗1小時代替熱水處理。 (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 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)_竹 476833 B7 經濟部中央標準局負工消費合作社印製 五、發明説明(45 ) 〇 (NI CO C&lt;I ω Ο 卜 CO LO LO 卜 CJD 〇〇 ς〇 CNl ω 呀 CNJ CO CO τ-Η LO 次 LO r-H CO Od Ο CM CO ς〇 卜 卜 〇〇 LO CO CNl 卜 CO 卜 LO ① LO CM LO &lt;=&gt; r-H CO CM ο oo oo r-H &lt;=&gt; 1—Η 卜 1—Η r-H Τ-Η CO QO CNl 卜 LO 卜 CD LO 卜 C&lt;1 CO 次 LO CO CNl ω o oo &lt;NI r-H 呀 T—Η LO LO τ-Η CO oo CO C&lt;I ω CM 〇 r—1 CO ο 1—i CO oo m 輝 幻m Μ ♦ 回 T—H &lt;Π 回 LO ♦ 回 c=&gt; 1—Η B o \ 1 bo 镔 κ 瓣 +讲 燊 ^ 観荽5 (請先閲讀背面之注意事項再填寫本頁) 本纸张尺度適用中國國家標準(CNS ) A4規格(210X297公釐1 48 476833 A 7 B7 五、發明説明(46 ) 實施例2 7及對照_實例2 4 重複實施例2 5程序,但是利用慣用絲光處理機對於 在伸展狀態下同實施例2 5之針織紡織品,以1 6 w t % 苛性蘇打於2 5 °C預浸5 0秒代替熱水處理。同實施例 2 5,試驗該紡織品之清洗收縮率(經紗+緯紗)及其頂 破强度。結果示於表1 6。 對照實例2 4與實施例2 7相同,但是省略絲光處理 (請先閲讀背面之注意事項再填寫本頁) ••I裝·This paper is again applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm X 46 476833 A7 B7 V. Description of the invention (44) Example _ Example 26 and Comparative Tube Example 2 λ Repeat the procedure of Example 25, but use The conventional mercerizing machine was pre-soaked with 16 wt% caustic soda at 25 ° C for 50 seconds in the stretched state of the knitted textile of Example 21 before liquid ammonia treatment. The textile was tested in the same manner as in Example 25. Washing shrinkage (warp + weft) and its burst strength. The results are shown in Table 15. Comparative Example 23 is the same as Example 26, but it is washed at 60 ° C for 1 hour in the non-stretched state instead of hot water. (Please read the notes on the back before filling out this page) The paper size printed by the Employees' Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs applies the Chinese National Standard (CNS) A4 specification (210X297 mm) _Bamboo 476833 B7 Central Standard of the Ministry of Economic Affairs Printed by the Bureau ’s Consumer Cooperatives. 5. Description of the invention (45) 〇 (NI CO C &lt; I ω Ο 卜 CO LO LO 卜 CJD 〇〇ς〇CNl ω Ya CNJ CO CO τ-Η LO times LO rH CO Od 〇 CM CO ς〇 卜卜 〇〇 LO CO CNl CO bl LO ① LO CM LO &lt; = &gt; rH CO CM ο oo oo rH &lt; = &gt; 1—Η bl 1—Η rH Τ-Η CO QO CNl bl LO bl CD LO bl C &lt; 1 CO secondary LO CO CNl ω o oo &lt; NI rH Ah T—Η LO LO τ-Η CO oo CO C &lt; I ω CM 〇r—1 CO ο 1—i CO oo m illusory m Μ ♦ Back to T—H &lt; Π Back to LO ♦ Back to c = &gt; 1—Η B o \ 1 bo 镔 κ flap + speak 燊 観 荽 5 (Please read the precautions on the back before filling this page) This paper size applies Chinese National Standard (CNS) A4 Specifications (210X297 mm 1 48 476833 A 7 B7 V. Description of the invention (46) Example 2 7 and Control_Example 2 4 Repeat the procedure of Example 2 5 but use a conventional mercerizing machine for Example 2 in the extended state. Knitted textile of 5 was pre-soaked with 16 wt% caustic soda at 25 ° C for 50 seconds instead of hot water treatment. As in Example 25, the cleaning shrinkage (warp + weft) of the textile and its burst strength were tested. The results are shown in Table 16. Comparative Example 2 4 is the same as Example 2 7 except that the mercerizing treatment is omitted (please read the precautions on the back before filling in this page) •• I ·

、1T ... 經濟部中央標準局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐49 - 476833 A7 B7 五、發明説明(47 ) 經濟部中央標準局員工消費合作社印製 &lt;NI ω ο οο 呀 CO ① CO CO 呀 〇 CNI 卜 (Nl οο (Μ LO CO σ&gt; CO LO LO 次 呀 οα ω ο ΟΟ ς〇 LO 卜 CNI OO 卜 LO τ*Η 卜 &lt;=&gt; LO LO 卜 LO CNI CO &lt;ΝΙ ω ο σ&gt; CNI l-H 05 t-H r—H oo LO 〇 τ-Η 卜 &lt;νι CM LO LO CO CO 卜 卜 呀 οα ο LO CO 1—H T-H LO l-H 05 LO 1—t LO CO 卜 οα CO oo &lt;NI σ&gt; oo 0¾ CO oo &lt;!□ fnl 回 回 1 Ο L=i CD Μ £ L-L J 5 m B o \ m CCQ to 1 bO 骢 m +讲 激 鍵婪3 (請先閲讀背面之注意事項再填寫本頁) •I裝· 訂 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐X 50 476833 經濟部中央標準局員工消費合作社印製 A7 _ B7五、發明説明(48 ) 根據本發明,可使含纖維素纖維結構具有經改良之防 皴性或防縮性而不會有紡織品强度的實質損失。特別是, 可賦予極薄且低强度紡織品經改良之防皴或防縮性而且其 維持可接受强度。該具體化實例中,防縮處理後接著樹脂 處理,可以進一步改善紡織品强度與防鮍或防縮性質間之 平衡,並使紡織品强度損失最小化。 雖然已說明某些較佳具體化實例,但是只要在本發明 範疇內,按照上述解釋可對其做改良或變化,本發明可以 特定說明以外之方式進行。 附圖簡沭 圖1係顯示實施例1 8和對照實例1 5中經處理紡織 品之乾燥防皺性質與抗張强度的圖。 圖2係顯示實施例19和對照實例16中經處理紡織 品之·乾燥防皺性質與抗張强度的圖。 _ 圖3係顯示實施例2 0和對照實例1 7中經處理紡織 品之乾燥防皺性質與抗張强度的圖。 圖4係顯示實施例21和對照實例18中經處理紡織 品之乾燥防皺性質與抗張强度的圖。 圖5係顯示實施例2 2和對照實例1 9中經處理紡織 品之乾燥防皺性質與抗張强度的圖。 圖6係顯示實施例2 3和對照實例2 0中經處理紡織 品之乾燥防皺性質與抗張强度的圖。 本&amp;張尺度適用中國國家標準(CNS)A4規格( 210X297公釐i 51 . (請先閱讀背面之注意事項再填寫本頁), 1T ... Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economics The paper standards are applicable to Chinese National Standards (CNS) A4 specifications (210 × 297 mm 49-476833 A7 B7) V. Description of the invention (47) Employees ’Central Standards Bureau of the Ministry of Economy Printed by the cooperative &lt; NI ω ο οο Ye CO ① CO CO Ye 〇CNI bl (Nl οο (Μ LO CO σ &gt; CO LO LO times οα ω ο ΟΟ ς〇LO bl CNI OO bl LO τ * Η bl) = &gt; LO LO bl LO CNI CO &lt; ΝΙ ω ο σ &gt; CNI lH 05 tH r—H oo LO 〇τ-Η bl &lt; νι CM LO LO CO CO bl οα ο LO CO 1—H TH LO lH 05 LO 1—t LO CO bl οα CO oo &lt; NI σ &gt; oo 0¾ CO oo &lt;! fnl returns 1 〇 L = i CD Μ £ LL J 5 m B o \ m CCQ to 1 bO 骢 m + Stress Key Greed 3 (Please read the notes on the back before filling out this page) • I Pack · The size of the paper is applicable to the Chinese National Standard (CNS) A4 specification (210X 297mm X 50 476833 Staff Consumption of the Central Standards Bureau of the Ministry of Economic Affairs Cooperative printed A7 _ B7 V. Description of the invention (48) According to the present invention, The vitamin fiber structure has improved mothproof or shrinkproof properties without substantial loss of textile strength. In particular, it can impart very thin and low-strength textiles with improved mothproof or shrinkproof properties while maintaining acceptable strength. In this embodiment, the anti-shrinking treatment followed by the resin treatment can further improve the balance between the strength of the textile and the anti-shrinkage or anti-shrinkage properties, and minimize the loss of the strength of the textile. Although some preferred embodiments have been described, as long as the Within the scope of the present invention, it can be improved or changed according to the above explanation, and the present invention can be carried out in a manner other than the specific description. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 shows the drying prevention of treated textiles in Example 18 and Comparative Example 15 A graph showing wrinkle properties and tensile strength. Figure 2 is a graph showing the dry wrinkle resistance and tensile strength of the treated textiles in Example 19 and Comparative Example 16. _ Figure 3 is a graph showing Example 20 and Comparative Example 1. A graph of the dry wrinkle resistance and tensile strength of the treated textiles in 7. FIG. 4 shows the drying of the treated textiles in Example 21 and Comparative Example 18. FIG nature and wrinkled tensile strength. Fig. 5 is a graph showing the dry wrinkle resistance and tensile strength of the treated textiles of Examples 22 and 19 of Comparative Example 19. Fig. 6 is a graph showing the dry wrinkle resistance and tensile strength of the treated textiles of Example 23 and Comparative Example 20; This &amp; Zhang scale is applicable to China National Standard (CNS) A4 specifications (210X297mm i 51. (Please read the precautions on the back before filling this page)

Claims (1)

A8 B8 C8 D8 六、申請專利範圍 附件1 a : 第8 6 1 0 6 8 2 1號專利申請案 中文申請專利範圍修正本 民國89年12月修正 1 . 一種纖維素纖維紡織品防縮處理用之方法,包括 步驟: 以液態氨處理該纖維紡織品;及 在伸展或非伸展狀態以熱水或苛性鹼處理該纖維紡織 品, 其中熱水處理係以1 0 0至1 5 0 °C溫度之熱水進行 ;苛性鹼處理係使用苛性鹼濃度爲0 . 1至4 0重量%之 苛性鹼水溶液於—1 0 °C至1 5 0 °C溫度下進行。 2 ·如申請專利範圍第1項之方法,其中苛性鹼處理 係使用苛性鹼濃度爲0 . 1至1 0重量%之苛性鹼水溶液 於高於9 0°C至1 5 0°C之溫度下進行。 3.如申請專利範圍第1項之方法,其中苛性鹼處理 係使用苛性鹼濃度爲1 0至4 0重量%之苛性鹼水溶液於 一 1 0 °C至9 0 °C之溫度下進行。 4·如申請專利範圍第1項之方法,其中該纖維素纖 維紡織品係由天然纖維素構成。 5.如申請專利範圍第1項之方法’其中該纖維素纖 維係由再生纖維素構成。 6 · —種纖維素纖維紡織品防縮處理用之方法,包括 步驟: 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) --------訂 -----l· 丨·. (請先閱讀背面之注意事項再填寫本頁)A8 B8 C8 D8 VI. Scope of Patent Application Annex 1 a: Patent Application No. 8 6 1 0 6 8 2 Chinese Application for Patent Scope Amendment Dec. 89 of the Republic of China Amendment 1. A method for shrinkage treatment of cellulose fiber textiles Including the steps of: treating the fiber textile with liquid ammonia; and treating the fiber textile with hot water or caustic in the stretched or non-stretched state, wherein the hot water treatment is performed with hot water at a temperature of 100 to 150 ° C ; Caustic treatment is carried out using a caustic aqueous solution having a caustic concentration of 0.1 to 40% by weight at a temperature of -10 ° C to 150 ° C. 2. The method according to item 1 of the scope of patent application, wherein the caustic treatment uses a caustic aqueous solution having a caustic concentration of 0.1 to 10% by weight at a temperature higher than 90 ° C to 150 ° C. get on. 3. The method according to item 1 of the patent application range, wherein the caustic treatment is carried out using a caustic aqueous solution having a caustic concentration of 10 to 40% by weight at a temperature of 10 ° C to 90 ° C. 4. The method of claim 1 in which the cellulose fiber textile is composed of natural cellulose. 5. The method according to item 1 of the scope of patent application, wherein the cellulose fiber is composed of regenerated cellulose. 6 · —A method for shrink-resistant treatment of cellulose fiber textiles, including the steps: This paper size applies to China National Standard (CNS) A4 (210 X 297 mm) -------- Order ----- l · 丨 ·. (Please read the notes on the back before filling this page) 經濟部智慧財產局員工消費合作社印製 476833 A8B8C8D8 六、申請專利範圍 以液態氨處理該纖維紡織品; 在伸展或非伸展狀態下,以熱水或苛性鹼處理該纖維 紡織品,以及 以樹脂處理該纖維紡織品。 7 ·如申請專利範圍第6項之方法,其中該樹脂處理 係使用纖維素反應性N -羥甲基化合物。 8·如申請專利範圍第6項之方法’其中該樹脂處理 係使用甲醛。 請 先 閲 讀 背 之 注 意 事 項 ¥ 本 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 476833 A8B8C8D8 6. Application for patents The fiber textile is treated with liquid ammonia; the fiber textile is treated with hot water or caustic in the stretched or unstretched state, and the fiber is treated with resin textile. 7. The method of claim 6 in the scope of patent application, wherein the resin treatment uses a cellulose-reactive N-methylol compound. 8. The method according to item 6 of the patent application, wherein the resin treatment uses formaldehyde. Please read the memorandum items in the back first. This is printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs. The paper size applies to the Chinese National Standard (CNS) A4 (210 X 297 mm).
TW86106821A 1996-05-23 1997-05-21 Shrink-proof treatment of cellulosic fiber textile TW476833B (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP15047096 1996-05-23
JP08260166A JP3073446B2 (en) 1996-05-23 1996-09-10 Method for shrink-proofing regenerated cellulosic fiber structure
JP26016996A JP3073447B2 (en) 1996-05-23 1996-09-10 Method for preventing shrinkage of natural cellulosic fiber structure
JP26249096A JP3154149B2 (en) 1996-09-11 1996-09-11 Resin processing method for cellulosic fiber-containing structure
JP28134296 1996-10-02

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