TW461927B - Textile finishing process - Google Patents

Textile finishing process Download PDF

Info

Publication number
TW461927B
TW461927B TW88104401A TW88104401A TW461927B TW 461927 B TW461927 B TW 461927B TW 88104401 A TW88104401 A TW 88104401A TW 88104401 A TW88104401 A TW 88104401A TW 461927 B TW461927 B TW 461927B
Authority
TW
Taiwan
Prior art keywords
textile
textiles
formaldehyde
elastomer
item
Prior art date
Application number
TW88104401A
Other languages
Chinese (zh)
Inventor
George L Payet
Original Assignee
American Textile Solutions Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US09/163,319 external-priority patent/US6511928B2/en
Priority claimed from US09/267,654 external-priority patent/US6375685B2/en
Application filed by American Textile Solutions Inc filed Critical American Textile Solutions Inc
Application granted granted Critical
Publication of TW461927B publication Critical patent/TW461927B/en

Links

Landscapes

  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

A process for treating a textile fabric to impart or enhance at least one property of the fabric comprising: introducing the fabric into an aqueous formaldehyde containing solution to provide a wet pickup of an effective amount of the solution by the fabric, applying to the fabric an effective amount of a catalyst for catalyzing a reaction between formaldehyde and the fabric; thereafter exposing the wet fabric to a temperature of at least about 300 DEG F to react the formaldehyde with the fabric to impart or enhance the property of the fabric before there is a substantial loss of formaldehyde from the exposed fabric.

Description

經濟部智慧財產局員工消費合作社印製 461927 , A7 ' _B7 五、發明説明(ί ) 發明背景 發明領域 本發明係有關於一種織物整理方法,其係使用甲醛水 溶液處理不同的紡織品’包括含有纖維素纖維之紡織品和 含有蛋白質纖維之紡織品。該方法亦應用至至含有上述與 不同纖維組合之紡織品’例如合成纖維,如聚酯。使用甲 醛做爲反應性成份的織物整理方法係爲習知,但是具有許 多缺點。本發明係有關於使用甲醛水溶液的新穎織物整理 方法,組成物及經處理紡織品 粗關前案的敘述· 有許多種習知之方法係使用甲醛處理織物紡織品。這 些欲被處理的織物紡織品包括含有例如羊毛和絲的蛋白質 纖維。纖維素纖維包括棉和螺縈。這些處理方法包括織物 之樹脂或聚合物處理,但是這些步驟爲昂貴且無法令人滿 意。另一種處理織物的方法,特別爲含纖維素纖維之織物 ,係爲一種壓燙持久性方法,其藉由甲醛提供纖維素分子 之耐久性交聯,因此對於含其等之紡織品和產物產生耐久 性抗皺祈和平整乾燥性質。這些欲被處理之織物紡織品通 常爲棉/混紡紡織品。其他的合成纖維,例如聚酯和相似 者,常包含在這些紡織品中以提供額外的性質。例如,聚 酯纖維被加至棉纖維以形成棉/聚酯混紡物。這些聚酯纖 維之加入可補償棉纖維因爲甲醛處理所損失的強度。這些 問題已在那些習知的方法中遇見。至今仍未硏發明一種簡 單,可重現,和完全令人滿意的低成本甲醛處理方法,特 ____;___:_3___________ 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) (請先閲讀背面之注意事項再填寫本頁) ,δτ 4 6 1 927 A7 B7 五、發明説明(>) 別爲壓烫持久性方法。 夙知可使用甲醛處理纖維素物質,如同於美國專利權 號2,243,765中所証實者。該專利敘及一種使用含有少量 酸催化劑之甲醛水溶液,在使反應接近平衡的時間和溫度 之下處理纖維素之方法。在進行該方法時,被加至纖維素 之甲醛溶液比率必需至少使該纖維素一直維持在完全溶脹 狀態。使用該甲醛和酸催化劑溶液處理的時間和溫度各不 相同,當溫度降低時所需之時間急劇地增加。如果需要時 ,產物可藉由洗濯和乾燥分離出,較佳在溫度爲大約212°F 。依據該方法得到之產物據稱可顯示出濕強度並不增加且 具有高度的吸水性,增高的鈹折阻抗性,及對一些直接染 料具有稍微增加的親和性。 近幾年來額外的方法已被設計爲處理含纖維素纖維的 產物用以賦予這些產物保留耐久性皺折,抗皺性和平整乾 燥性質。如同所述及者,甲醛已被該等纖維素物質交聯而 生成這些產物。亦已了解可使用樹脂或尿素-甲醛的預縮合 物或經取代之尿素-甲醛種類.以產生經樹脂處理之壓燙持久 性產物。如同於美國專利權號3,841,832中所提及者,甲 醛雖然已對棉整理領域做了顯著的貢獻,結果仍極不完善 。例如,在某些案例中,因爲甲醛交聯反應的控制困難, 甲醛交聯處理顯示缺乏可重現性。如同於美國專利權 4,396,390中所述,不具可重現性特別發生在商用規模上。 更甚者,無法接受的紡織品強度損失亦已經在許多使 用甲醛水溶液之處理方法中發現。當高的硬化溫度與酸或 (請先閱讀背面之注意事項再填寫本頁) -6 Γ 經濟部智慧財產局員X消費合作杜印製 尽、我張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 4 6 1927 經濟部智慧財產局員工消費合作杜印製 A7 B7 五、發明説明("7 ) 潛在的酸催化劑一起使用時,其常發生可損害棉強度之過 度反應和降解作用。另一方面,當溫度爲106°F或更低時欲 達到可重現性,通常需要更長的反應或整理時間,致使該 方法相當地不具有經濟效益。有關於此的溶液於美國專利 權號4,108,598中提及,其中的全部揭示倂於本文用爲參 考。螺縈,例如再生纖維素(纖維膠和銅銨),於該專利權 中稱爲含纖維素之纖維,其對前案而言爲習知者。 發明槪沭 本發明係有關於一種織物整理方法,其用於處理織物 纖維致使或增強紡織品的至少一種性質。此類性質包括紡 織品的壓燙持久性性質,且較佳爲在該整理方法期間壓烫 持久性性質可使該紡織品降低紡織品強度的損失。進一步 的性質包括紡織品縮水性的降低及/或經處理紡織品水洗 能力的改良。本發明亦包括使用於該方法之組成物或成份 ,及經該方法處理的紡織品。 本發明包括一種處理織物紡織品以達到或增強該紡織 品至少一種性質的方法’該方法包含將該紡織品置入含甲 醛之水溶液內以得到在該紡織品中有效量溶液之濕吸收 (wet pickup),有效量之催化劑施加至該紡織品內用以催 化甲醛和紡織品之間的反應;和將該濕紡織品曝露至溫度 爲至少約300°F,使甲醛由該經曝露紡織品中實質移除之前 令甲醛與紡織品反應以達到或增強紡織品之性質。 該水溶液可施用至該紡織品,較佳者係藉由將該紡織 品置入水溶液中以得到在該紡織品內有效量溶液之濕吸收 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁)Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 461927, A7 '_B7 V. Description of the invention (ί) BACKGROUND OF THE INVENTION Field of the Invention The present invention relates to a method of fabric finishing, which uses a formaldehyde aqueous solution to treat different textiles, including cellulose. Fibrous textiles and textiles containing protein fibers. This method is also applicable to textiles' such as synthetic fibers, such as polyester, which contain the above-mentioned combination with different fibers. Fabric finishing methods using formaldehyde as a reactive ingredient are well known, but have many disadvantages. The present invention relates to novel fabric finishing methods, compositions, and treated textiles using a formaldehyde aqueous solution. There are many conventional methods for treating textile fabrics with formaldehyde. These fabric textiles to be treated include protein fibers containing, for example, wool and silk. Cellulose fibers include cotton and snails. These treatments include resin or polymer treatment of the fabric, but these steps are expensive and unsatisfactory. Another method for treating fabrics, especially cellulose fiber-containing fabrics, is a method of embossing and permanence, which provides durable cross-linking of cellulose molecules by formaldehyde, and thus produces durability for textiles and products containing them. Anti-wrinkle prayer and leveling and drying properties. These fabric textiles to be treated are usually cotton / blend textiles. Other synthetic fibers, such as polyester and the like, are often included in these textiles to provide additional properties. For example, polyester fibers are added to cotton fibers to form a cotton / polyester blend. The addition of these polyester fibers can compensate for the strength lost by cotton fibers due to formaldehyde treatment. These problems have been encountered in those conventional methods. So far, we have not invented a simple, reproducible, and completely satisfactory low-cost formaldehyde treatment method, especially ____; ___: _3___________ This paper size applies the Chinese National Standard (CNS) A4 specification (210X 297 mm) ( Please read the precautions on the back before filling in this page), δτ 4 6 1 927 A7 B7 V. Description of the invention (>) Don't be a permanent method of pressing. It is known that cellulose materials can be treated with formaldehyde, as demonstrated in U.S. Patent No. 2,243,765. The patent describes a method of treating cellulose using a formaldehyde aqueous solution containing a small amount of an acid catalyst under a time and temperature that allows the reaction to approach equilibrium. When performing this method, the ratio of the formaldehyde solution added to the cellulose must at least maintain the cellulose in a fully swelled state. The time and temperature of the treatment with this formaldehyde and acid catalyst solution are different, and the time required when the temperature is lowered sharply increases. If necessary, the product can be isolated by washing and drying, preferably at a temperature of about 212 ° F. The product obtained according to this method is said to show no increase in wet strength and high water absorption, increased resistance to beryllium fold resistance, and slightly increased affinity for some direct dyes. In recent years additional methods have been designed to treat cellulose fiber-containing products to give these products retention of durable wrinkles, wrinkle resistance, and leveling and drying properties. As mentioned, formaldehyde has been crosslinked by these cellulosic materials to produce these products. It is also known that resins or urea-formaldehyde precondensates or substituted urea-formaldehyde species can be used to produce resin-treated, stamped, durable products. As mentioned in US Patent No. 3,841,832, although formaldehyde has made a significant contribution to the field of cotton finishing, the results are still extremely imperfect. For example, in some cases, due to the difficulty in controlling the formaldehyde cross-linking reaction, the formaldehyde cross-linking treatment showed a lack of reproducibility. As described in U.S. Patent No. 4,396,390, non-reproducibility occurs particularly on a commercial scale. What's more, unacceptable loss of textile strength has been found in many treatments using aqueous formaldehyde solutions. When the high hardening temperature and acid or (please read the precautions on the back before filling this page) -6 Γ Member of the Intellectual Property Bureau of the Ministry of Economic Affairs X Consumption Du Du printed, our specifications are applicable to China National Standard (CNS) A4 specifications ( 210X297 mm) 4 6 1927 Consumption cooperation between employees of the Intellectual Property Bureau of the Ministry of Economic Affairs, printed by A7 B7 5. Description of invention (" 7) When a potential acid catalyst is used together, overreaction and degradation that can damage the strength of cotton often occur . On the other hand, to achieve reproducibility when the temperature is 106 ° F or lower, a longer reaction or finishing time is usually required, making the method considerably less economical. Related solutions are mentioned in U.S. Patent No. 4,108,598, the entire disclosure of which is hereby incorporated by reference. Snails, such as regenerated cellulose (cellulose and copper ammonium), are referred to in this patent as cellulose-containing fibers, which are known to the previous case. Invention 槪 沭 The present invention relates to a fabric finishing method for treating fabric fibers to cause or enhance at least one property of a textile. Such properties include the permanence properties of a woven fabric, and preferably the permanence properties during the finishing process can reduce the textile's loss of textile strength. Further properties include reduced textile shrinkage and / or improved washability of treated textiles. The invention also includes compositions or ingredients used in the method, and textiles treated by the method. The present invention includes a method of treating a fabric textile to achieve or enhance at least one property of the textile. The method includes placing the textile in an aqueous solution containing formaldehyde to obtain a wet pickup of an effective amount of the solution in the textile, effectively An amount of catalyst is applied to the textile to catalyze the reaction between formaldehyde and the textile; and exposing the wet textile to a temperature of at least about 300 ° F, allowing formaldehyde and the textile to be substantially removed from the exposed textile. React to achieve or enhance the properties of textiles. The aqueous solution can be applied to the textile, preferably the textile is placed in the aqueous solution to obtain an effective amount of the solution in the textile. The paper size is applicable to the Chinese National Standard (CNS) A4 (210X297 mm) (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 4 6 19 2 7 a7 B7 _ 五、發明説明(斗) 。在一個範圍中,該處理溶液包含一有效量之甲醛或甲醛 生成之物質與一催化劑用於催化甲醛與紡織品之間的反應 。在水溶液的起始施用之後,可能在環境溫度之下’該紡 織品曝露在溫度大約爲300°F使甲醛由該經曝露紡織品中實 質移除之前令甲醛與紡織品反應,致使達到或增強紡織品 之至少一種性質。此步驟可經由將紡織品置入具有溫度爲 至少大約300°F之加熱區中而達到。 含有纖維素纖維或蛋白質纖維的紡織品在存有彈性體 時與甲醛水溶液反應。藉由使用於含纖維素纖維之紡織品 壓燙持久性/無皺痕方法,在含有纖維素纖維之紡織品可 能得到良好的壓燙持久性性質且具有良好的強度保留性’ 及一致的結果。這個方法利用甲醛和具有彈性體的催化劑 對於含纖維素纖維之紡織品達到抗皺痕性’且同時在抗張 強度和撕裂強度上可降低損耗。聚矽氧烷彈性體較佳被使 用於該方法。該方法對於1〇〇%棉紡織品時特別有效° 同時包括在內者爲一種處理織物紡織品以增強該紡織 品至少一種性質之方法’其包含在環境溫度下使用甲醛水 溶液和催化劑處理該紡織品以催化甲醛和該紡織品之間的 反應;和將濕紡織品置入具有至少大約300 F昇局溫度之加 熱區域而將在環境溫度下處理之紡織品直接置於昇高的溫 度使甲醛與紡織品反應而增強紡織品的性質。 在本發明的另一個範圍中’該種使用甲醛處理織物紡 織品以增強該紡織品至少一種性質之方法係包含以甲酸處 理含有選自包含纖維素纖維和蛋白質纖維之妨織品’而使 -____ .___6------一 本紙張尺度適用中國國家標準(CNS ) A4規格(2l〇X297公釐) (請先聞讀背面之注意事項再填寫本頁)Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 4 6 19 2 7 a7 B7 _ 5. Description of the invention (bucket). In one range, the treatment solution contains an effective amount of formaldehyde or a substance generated by formaldehyde and a catalyst for catalyzing the reaction between formaldehyde and textiles. After the initial application of the aqueous solution, it may be at ambient temperature that the textile is exposed to a temperature of about 300 ° F before the formaldehyde is substantially removed from the exposed textile. The formaldehyde is allowed to react with the textile so that at least the textile is reached or enhanced. A nature. This step can be achieved by placing the textile in a heated zone having a temperature of at least about 300 ° F. Textiles containing cellulose fibers or protein fibers react with aqueous formaldehyde in the presence of elastomers. By using the pressurization / wrinkle-free method for cellulose fiber-containing textiles, it is possible to obtain good pressurization durability and good strength retention 'and consistent results in textiles containing cellulose fibers. This method uses formaldehyde and a catalyst with an elastomer to achieve wrinkle resistance ' for textiles containing cellulose fibers, while reducing loss in tensile strength and tear strength. Polysiloxane elastomers are preferably used in this method. This method is particularly effective for 100% cotton textiles. Also included is a method of treating a textile textile to enhance at least one property of the textile. It includes treating the textile with an aqueous formaldehyde solution and a catalyst at ambient temperature to catalyze formaldehyde. Reaction with the textile; and placing wet textiles in a heated area with a local temperature of at least about 300 F and placing textiles treated at ambient temperature directly at elevated temperatures to react formaldehyde with the textile to enhance the textile nature. In another scope of the present invention, 'The method of treating a fabric textile with formaldehyde to enhance at least one property of the textile comprises treating with formic acid a fabric containing a fiber selected from the group consisting of cellulose fibers and protein fibers' so that -____.___ 6 ------ One paper size applies Chinese National Standard (CNS) A4 specification (210 × 297 mm) (Please read the precautions on the back before filling this page)

'1T 經濟部智慧財產局員X消費合作社印製 -46 1 927 五、發明説明($ ) 甲醛與該纖維素或蛋白質纖維反應’及接枝一彈性體至該 纖維素或蛋白質纖維上。 本發明的進一步範圍包括一種後處理方法而由紡織品 中移除過量甲醛的方法’其係藉由以有機酸之甲醛移除劑 水溶液淸洗經處理的紡^品。因爲包括甲醛之處理化學品 濃度依經處理的紡織品而改變’甲醛移除劑的濃度可由制 式的實驗來決定。 該方法亦包括使用尿素的或其衍生物以增加紡織品的 強度。該種經處理紡織品亦屬於本發明的一部份。 發明仍具有的進一步範圍中,穩定的化學組成物或成 份亦可使用於製備用於本發明方法中的處理水溶液。 可施用至該方法紡織品且包括水和選用成分之該等化 學組成物可於該方法進行期間可與水溶液系統共同施用至 該紡織品,或連續地在任何時間內施用,只要不同組成物 連續地加至紡織品時在該紡織品中並不妨礙處理所需的水 平。 較佳具體眚施例的敘沭 可使用本發明方法處理之含纖維素纖維的紡織品包括 棉或棉混紡物所製成的布料。對於固定消費者所需之更佳 處理,即爲更多的無皺痕產品和在混紡紡織品中有更高的 含棉量,或較佳爲100%棉紡織品。對於完全以棉製成的紡 織品具有無皺痕且具有抗張強度和撕裂強度有極大的需求 。可得到100%棉紡織品,但僅限於較沈重的褲子或底部需 重壓的紡織品。不幸地,大部份無皴痕的含纖維素紡織品 尺度適用中國國家標準(CNS ) A4規格--~ (請先聞讀背面之注意事項再填寫本頁)'1T Printed by the Intellectual Property Bureau of the Ministry of Economic Affairs X Consumer Cooperative -46 1 927 V. Description of the Invention ($) Formaldehyde reacts with the cellulose or protein fiber' and grafts an elastomer onto the cellulose or protein fiber. A further scope of the present invention includes a post-treatment method for removing excess formaldehyde from textiles' by washing the treated textiles with an aqueous solution of a formaldehyde remover of an organic acid. Because the concentration of the treatment chemical including formaldehyde varies depending on the treated textile, the concentration of the 'formaldehyde remover' can be determined by standard experiments. The method also includes using urea or a derivative thereof to increase the strength of the textile. This treated textile also forms part of the invention. In a still further scope of the invention, stable chemical compositions or ingredients may also be used in the preparation of the treated aqueous solution used in the method of the invention. The chemical compositions that can be applied to the textile of the method and include water and optional ingredients can be co-applied to the textile with the aqueous system during the method, or continuously at any time, as long as the different compositions are continuously applied The level required in the textile is not impeded by the time it reaches the textile. A description of a preferred embodiment The textiles containing cellulose fibers which can be treated using the method of the present invention include cloths made of cotton or cotton blends. The better treatments required for stationary consumers are more wrinkle-free products and higher cotton content in blended textiles, or preferably 100% cotton textiles. There is a great demand for textiles made entirely of cotton that are wrinkle-free and have tensile and tear strength. 100% cotton textiles are available, but only for heavy trousers or textiles that require heavy pressing on the bottom. Unfortunately, most of the cellulose-free textiles without nicks apply the Chinese National Standard (CNS) A4 specifications-(Please read the precautions on the back before filling this page)

461927 A7 B7 五、發明説明(6 ) 係在甲醛系統中處理,對於撕裂和抗張強度的損耗增高, 因此該經處理的紡織品變得較脆弱。其可能過於脆弱而無 法成爲商業產品。 所有,當處理方法中所使用的化學品數量增加以得到 經處理紡織品中可接受的抗皺痕時,對於撕裂和抗張強度 的損耗可能降至無法接受的水平。聚酯纖維最常與棉纖維 摻合而補償經處理棉在強度上的損耗因而形成最常見的棉 /聚酯混紡紡織品。最常使用至多爲65%之聚酯量。因爲 在混紡物中存有聚酯纖維或其他的合成纖維,這些混紡的 紡織品爲足夠地強韌但是無法具有舒適性或如同含較高棉 量,或最期望地100%棉,紡織品的觸感。本發明的方法可 克服前案技藝中的缺點,其可在混紡物中存有更高百分率 的棉,甚至可處理輕薄或襯衫的100%含棉紡織品而達到商 業上可接受的無皴痕標準,且使紡織品仍維持商業上可接 受的適當強度。經處理紡織品的商業上可接受性爲本發明 方法的終極目標。 本發明的一個較佳範圍包含一種處理含棉紡織品,包 括100%含棉紡織品,的壓烫持久性方法,其係藉由在存有 一彈性體,較佳爲聚矽氧烷彈性體,使用甲醛水溶液和足 以催化甲醛和纖維素之間的交聯反應之催化劑處理含纖維 素纖維紡織品,在存有催化劑且在甲醛與纖維素反應之前 不實質移除甲醛的條件下熱硬化經處理的含纖維素纖維紡 織品以改良紡織品皺痕抗性且同時降低抗張強度和撕裂 強度的損耗。較佳爲含纖維素的紡織品在完全溶脹狀態。 一 8____— (請先閱讀背面之注意事項再填寫本頁) 訂 經濟部智慧財產局員工消費合作社印製 ©Yll' 本紙張尺度適用中國國家標準(CNS ) A4規格(21〇><297公釐) 46 1927 A7 B7 ^aio.23 年月日夕 經濟部智慧財產局員工消費合作社印製 五、發明說明(7) 彈性體可連同甲醛和催化劑水溶液施用至紡織品。此 係將所有的處理化學品同時施用至在一種處理溶液中的紡 織品。然而,所必需的化學品’包括水和選用的成份,可 在方法進行期間的任何時間內依續地施用至紡織品內,只 要該順序不妨礙紡織品中所需之處理水平。彈性體之取得 通常爲商用的乳化劑。可使用於本發明方法之含特定彈性 體的組成物包括在含有少量彈性體之組成物倒至開放表面 且放置乾燥時乾燥形成之薄膜具有彈性體性質者。此爲一 種簡單測試以決定彈性體是否在該方法中有用。如果所選 用的彈性體造成經處理的紡織品爲親水性則更爲有利。親 水性的紡織品,亦即並不排斥水者,通常對穿著者而言具 有更高舒適性。本發明之含親水性(遇水可濕)壓燙持久 性纖維的紡織品具有甲醛交聯物及彈性體接枝物。該紡織 品較佳具有聚矽氧烷彈性體接枝物且該包括螺縈的紡織品 /較佳爲含纖維素。 雖然可使用任何彈性體,聚矽氧烷彈性體爲特別佳者 。任何的聚矽氧烷彈性體可被使用於本發明。聚矽氧烷彈 性體爲習知的材料。聚矽氧烷彈性體爲下列通式.地具有一 主鏈係由砂和氧組成,其中有機取代基連接至矽原子且包 含η個重複單位: R1461927 A7 B7 V. Description of the invention (6) The treatment in the formaldehyde system increases the loss of tear and tensile strength, so the treated textile becomes more fragile. It may be too fragile to become a commercial product. Therefore, as the amount of chemicals used in the treatment process increases to achieve acceptable resistance to wrinkles in treated textiles, the loss of tear and tensile strength may fall to unacceptable levels. Polyester fibers are most often blended with cotton fibers to compensate for the loss of strength in treated cotton and form the most common cotton / polyester blended textile. The most commonly used polyester amount is up to 65%. Because of the presence of polyester or other synthetic fibers in the blend, these blended textiles are sufficiently strong but not comfortable or have a higher cotton content, or the most desirable 100% cotton, textile touch . The method of the present invention can overcome the shortcomings of the previous case technology, it can store a higher percentage of cotton in the blend, and can even handle light or thin 100% cotton-containing textiles to achieve a commercially acceptable standard without nicks. While maintaining the proper strength of the textile that is commercially acceptable. The commercial acceptability of treated textiles is the ultimate goal of the method of the invention. A preferred range of the present invention includes a method for treating the endurance of cotton-containing textiles, including 100% cotton-containing textiles, by using an elastomer, preferably a polysiloxane elastomer, using formaldehyde An aqueous solution and a catalyst sufficient to catalyze the cross-linking reaction between formaldehyde and cellulose treat cellulose-containing fiber textiles, and heat-treat the treated fiber-containing fibers in the presence of a catalyst and without substantially removing formaldehyde before the formaldehyde reacts with cellulose. Plain fiber textiles to improve textile wrinkle resistance while reducing loss of tensile and tear strength. It is preferred that the cellulose-containing textile is in a fully swelled state. 8 ____— (Please read the notes on the back before filling this page) Order printed by the Intellectual Property Bureau of the Ministry of Economic Affairs, printed by the Consumer Cooperatives © Yll 'This paper size applies the Chinese National Standard (CNS) A4 specification (21〇 > < 297 (Mm) 46 1927 A7 B7 ^ aio. 23 Printed by the Consumers' Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs on March 23, 2015. 5. Description of the invention (7) Elastomers can be applied to textiles together with formaldehyde and aqueous catalyst solutions. This is the simultaneous application of all treatment chemicals to the textile in one treatment solution. However, the necessary chemicals', including water and selected ingredients, can be applied to the textile one after the other at any time during the method as long as the sequence does not interfere with the level of processing required in the textile. The acquisition of elastomers is usually a commercial emulsifier. The specific elastomer-containing composition which can be used in the method of the present invention includes those having a elastomeric property when the composition containing a small amount of elastomer is poured onto an open surface and the film formed by drying when left to dry. This is a simple test to determine if an elastomer is useful in this method. It is even more advantageous if the elastomer chosen makes the treated textile hydrophilic. Water-repellent textiles, that is, those that do not repel water, are generally more comfortable for the wearer. The textile containing hydrophilic (wetted with water) embossed permanent fibers has formaldehyde cross-linkers and elastomer grafts. The textile preferably has a polysiloxane elastomer graft and the textile including snails / preferably contains cellulose. Although any elastomer can be used, polysiloxane elastomers are particularly preferred. Any polysiloxane elastomer can be used in the present invention. Polysiloxane elastomers are known materials. The polysiloxane elastomer has the following general formula. The ground has a main chain consisting of sand and oxygen, in which an organic substituent is connected to a silicon atom and contains η repeating units: R1

I -Si ~〇-——I -Si ~ 〇 -——

II

R ' n 9 本紙張尺度適用中國國豕標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再填寫本頁) ------— r 訂·?;-------線 461927 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(g) R和R >基轉可相同或不同,及例如包括低碳烷基, 例如甲基,乙基,丙基’苯基,或任何的這些基團經羥基 團,氟化物原子或胺基團取代;換句話說,反應性基團接 至纖維素,例如棉和螺縈。 使用於製造用於本發明聚矽氧烷彈性體之聚矽氧烷係 使用習知方法製得’其包括藉由水解鹵化有機矽而形成之 羥基有機矽化合物的縮合物。所需鹵化物的製備可藉由齒 化砂和格里納試劑之間的直接反應。另一種方法可基於石夕 烷與不飽和化合物,例如乙烯或乙炔,的反應。藉由蒸餾 分離出反應產物之後,鹵化有機矽可藉由小心地控制水解 而聚合並得到有用於本發明之聚矽氧烷聚合物。 例如,可使用經純化三元體(ter tramer)以鹼性催化 劑在212-302°F下聚合而得之彈性體,其分子量可使用單 官能性矽烷控制。硬化特性和性質可因爲使用-H,-0H,氟 烷基,烷氧基或乙烯基取代一些甲基,或使用熟於此藝者 所習用之塡充劑混合而有廣範圍的變化。 使用於本發明之聚矽氧烷彈性體爲具有高分子量之物 質,其適常由二甲基聚矽氧烷單位(單體)與一線性鏈連 接。這些物質一般含有一過氧化物類型之催化劑,其可造 成所形成亞甲基橋中的相鄰甲基之間之連接。所存有的交 聯通常因爲可形成較大的分子而改良在經處理纖維中聚矽 氧烷彈性體之耐久性。 另一種反應性聚矽氧烷聚合物類別爲如同於美國專利 權號4,184,004號中所述者係爲親水性有機聚矽氧烷三元 (請先閲讀背面之注意事項再填寫本頁)R 'n 9 The size of this paper is applicable to China National Standard (CNS) A4 (210 X 297 mm) (Please read the precautions on the back before filling this page) ------— r Order ·?;- ------ Line 461927 A7 B7 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 5. Description of the invention (g) R and R can be the same or different and include, for example, lower alkyl groups, such as methyl , Ethyl, propyl'phenyl, or any of these groups are substituted with hydroxyl groups, fluoride atoms or amine groups; in other words, reactive groups are attached to cellulose, such as cotton and spironium. The polysiloxane used in the production of the polysiloxane elastomer of the present invention is prepared using a conventional method 'which includes a condensate of a hydroxyorganosilicone compound formed by hydrolyzing a halogenated silicone. The required halide can be prepared by direct reaction between the toothed sand and the Grignard reagent. Another method may be based on the reaction of hexane with an unsaturated compound, such as ethylene or acetylene. After the reaction product is separated by distillation, the halogenated organosilicon can be polymerized by carefully controlling the hydrolysis and a polysiloxane polymer useful in the present invention can be obtained. For example, an elastomer obtained by polymerizing a purified ter tramer with a basic catalyst at 212-302 ° F can be used, and its molecular weight can be controlled using a monofunctional silane. Hardening characteristics and properties can vary widely by using -H, -0H, fluoroalkyl, alkoxy, or vinyl groups to replace some methyl groups, or by using admixtures known to those skilled in the art. The polysiloxane elastomer used in the present invention is a substance having a high molecular weight, which is usually connected by a dimethylpolysiloxane unit (monomer) to a linear chain. These materials generally contain a peroxide-type catalyst that can cause connections between adjacent methyl groups in the formed methylene bridge. The presence of cross-linking usually improves the durability of the silicone elastomer in the treated fiber because it can form larger molecules. Another type of reactive polysiloxane polymer is as described in U.S. Patent No. 4,184,004, which is a hydrophilic organic polysiloxane ternary (please read the precautions on the back before filling this page)

'II 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 經濟部智慧財產局員工消費合作社印製 4 6 1927 A7 B7 五、發明説明(气) 共聚物,其等爲彈性體且含有許多的反應性環氧基和許多 的聚氧化烯基,該專利之所有揭示倂於本文中以爲參考。 亦被倂於本文以爲參考者爲美國專利權4,3丨2,993號之揭 示,其所述及之甲矽烷基化聚醚可使用於發明方法中。 其亦可能製造一種反應性聚矽氧烷彈性體爲其中反應 性基足以與已經加至線性二甲基聚砂氧院聚合物的基質反 應。這些聚砂氧院能夠同時與纖維素基質及與大多數的蛋 白質纖維反應,旦其特徵在於在受質上具有極大耐久性之 聚矽氧烷聚合物,其甚至接近基質的壽命° 因此,可釋出反應產物之聚矽氧烷彈性體顯示出與基 質的化學反應遠易於與非反應性聚矽氧烷彈性體的反應’ 但是其並不意味非反應性聚矽氧烷彈性體無法使用於本方 法。如同於本文所附之表I和11所示,得自於不同製造商 之不同彈性體全顯示出增強的抗張強度和撕裂強度。彈性 體的聚矽氧烷聚合物已發現具有增加的強度,然而經簡易 乳化之聚矽氧烷油類(或潤滑劑)在抗張強度上並不增加 〇 含有甲醛,酸催化劑,彈性體和濕潤劑的水溶液系統 ,較佳係由相同之浴中塡塞至欲被處理的紡織品中確使溼 度含量爲基於紡織品之高於20重量百分率。然而,各種不 同的處理化學品可在方法之進行期間在各種不同的處理狀 態下依序地加入。這些步驟可安排得使該方法成爲一種連 續方法。該紡織品然後藉由曝露於高溫度下硬化。塡塞技 術對於本技藝係爲習知者,且通常包含將該紡織品通經一 尺度適用中國國家標準(CNS ) A4規格(210X29^5•釐) (請先閲讀背面之注意事項再填寫本頁)'II This paper size applies to China National Standard (CNS) A4 (210X297 mm) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 4 6 1927 A7 B7 V. Description of the invention (gas) Copolymer, which is an elastomer and Containing many reactive epoxy groups and many polyoxyalkylene groups, all the disclosures of this patent are incorporated herein by reference. Also disclosed herein as a reference is the disclosure of U.S. Patent No. 4,3,2,993, and the silylated polyethers described therein can be used in the inventive method. It is also possible to make a reactive polysiloxane elastomer in which the reactive groups are sufficient to react with a matrix that has been added to a linear dimethylpolyoxygen polymer. These polyoxygen hospitals can react with cellulose substrates and most protein fibers at the same time. Once they are characterized by a polysiloxane polymer with great durability in the substrate, it is even close to the life of the substrate. The polysiloxane elastomer that releases the reaction product shows that the chemical reaction with the matrix is far easier to react with the non-reactive polysiloxane elastomer ', but it does not mean that the non-reactive polysiloxane elastomer cannot be used in This method. As shown in Tables I and 11 attached hereto, different elastomers from different manufacturers all show enhanced tensile and tear strength. Elastomeric polysiloxane polymers have been found to have increased strength, but simply emulsified polysiloxane oils (or lubricants) do not increase tensile strength. Contains formaldehyde, acid catalysts, elastomers, and The aqueous solution system of the wetting agent is preferably stuffed from the same bath to the textile to be treated so that the moisture content is higher than 20% by weight based on the textile. However, a variety of different processing chemicals can be added sequentially in a variety of processing states during the course of the method. These steps can be arranged to make the method a continuous method. The textile is then hardened by exposure to high temperatures. Congestion technology is familiar to this art department, and usually includes applying the textile to a standard of China National Standard (CNS) A4 specification (210X29 ^ 5 • centimeter) (Please read the precautions on the back before filling this page )

461927 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明((〇) 水溶液,然後通過一擠壓滾筒以提供濕吸收爲由約50%至 100%或更高,通常約爲66%。反應物在水溶液中之濃度和 紡織品在處理溶液中之滞留時間可調整至可提供基於紡織 品重量(OWF)所需之反應物數量。 在本發明的一個較佳範圍中,紡織品在通經含有甲醛 和催化劑之化學處理浴之前先被預溼潤。預濕潤可單獨使 用水或含有濕潤劑之水溶液。對於一般地熟悉使用甲醛進 行壓烫持久性處琿含棉紡織品技術者而言爲習知之習用濕 潤劑可使用於該溶液,通常之數爲爲基於溶液重量之0.1% (0.1%固體OWF)。此造成基於紡織品重量之少量濕潤劑施 用至該紡織品。該濕潤劑可確使處理溶液依循正確方向進 入纖維之內,使得全部的纖維可使用該處理溶液處理,而 非僅止於纖維的外部。(若如此將會導致極差的處理)。對 於該方法不造成不利效應的任何濕潤劑均可使用。非離子 性濕潤劑爲較佳者,其係因爲離子性試劑可造成處理溶液 的破裂,尤其是彈性體乳液,因此,濕潤劑必需小心地選 擇,且較佳由熟於此藝者在實驗室中測試。此爲一種例行 的步驟。 使用水溶液預處理之進行可藉由將紡織品通經水浴, 然後通過滾筒移除過量的水份,或可藉由使用習用的低濕 度吸取設備,也就是真空設備等,且在分離的浴中施加處 理化學品之前控制在紡織品中的濕度量。其必需知道紡織 品達到處理浴時的濕度含量,因此可以決定且調整施加至 處理浴的化學品濃度,因此在曝露至高硬化溫度以得到所 (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隼(CNS )八4規格(210χ297公餐) 經濟部智慧財產局員工消費合作杜印製 46 1 927 A7 _ _ B7__ 五、發明説明(η ) 需處理水平之前可確知在紡織品中反應物之正確量。在施 加處理化學品之前的紡織品淫度量’在預濕潤的紡織品通 經處理浴後會稀釋該紡織品所『看見』的化學品數量。 上述之步驟,即習稱爲化學品水溶液之濕度在濕式施 用(wet on wet application),較之於化學品施加至乾燥 紡織品可產生比13%更高的強度。當處理濕性紡織品時其 縮水性比處理乾燥紡織品爲佳。 若不討論反應機制’一件事可確知者爲當紡織品已預 濕潤後可得到完全的濕潤及飽和’然而對於乾燥紡織品並 無法保証該紡織品和所有的纖維可達到相同程度的飽和與 溶脹。經發現,乾燥紡織品在使用化學處理水溶液塡塞時 不易均勻地濕潤。在濕度在濕式施用中,先施加水和濕潤 劑且在化學水溶液施加之前令其完全飽和。此爲一種施加 水和化學品的兩次停止連續方法的實施例。 不欲受任何理論所限制者,因爲該種施用應分佈至沒 有或較少溶液的區域,如果可目視一紡織品具有點狀的較 深濕潤區域與並未濕潤的區域相鄰’則較深濕潤區域含有 比應含的更多化學品。化學品濃度較高區域的處理會比具 有較少化學品的相鄰區域更多。因此差的濕潤或差的均勻 '性造成紡織品中弱的或過度處理的微小區域和強的未經處 理區域。該紡織品強度僅與最弱的點狀一樣好° 現在所觀察者爲在施加化學品之前使用水濕潤至50% 的紡織品被迅速浸漬於具有兩倍化學品濃度(對於已存於 紡織品中水的兩倍強度)之處理液中。當化學品溶液使用 __:___—---η-___一 本紙張尺度適用中國國家標準(CNS ) Α4規格(21〇Χ2.97公釐) (請先閲讀背面之注意事項再填寫本頁)461927 B7 Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs. 5. Description of the Invention ((〇) Aqueous solution, then passed through a squeeze roller to provide wet absorption from about 50% to 100% or higher, usually about 66%. The concentration of the reactants in the aqueous solution and the residence time of the textile in the treatment solution can be adjusted to provide the amount of reactants required based on the weight of the textile (OWF). In a preferred range of the present invention, the textile contains formaldehyde Pre-wet before the chemical treatment bath with catalyst. Pre-wet can be used by itself or aqueous solution containing wetting agent. For general familiarity with the use of formaldehyde for permanent pressing, cotton-containing textile technology is a customary wetting. Agents can be used in the solution, usually at 0.1% (0.1% solids OWF) based on the weight of the solution. This results in a small amount of wetting agent applied to the textile based on the weight of the textile. The wetting agent ensures that the treatment solution follows the correct direction Into the fiber, so that all the fibers can be treated with the treatment solution, not just the outside of the fiber. (If so, it will lead Resulting in very poor treatment). Any wetting agent that does not cause adverse effects to this method can be used. Non-ionic wetting agents are preferred, because ionic agents can cause cracking of the treatment solution, especially elastomer emulsions Therefore, wetting agents must be carefully selected and are preferably tested in the laboratory by those skilled in the art. This is a routine procedure. Pretreatment with aqueous solutions can be carried out by passing the textile through a water bath and then The drum removes excess water, or can use conventional low-humidity suction equipment, i.e., vacuum equipment, and control the amount of humidity in the textile before applying the treatment chemicals in a separate bath. It must know that the textile reaches The humidity content in the processing bath, so you can determine and adjust the concentration of chemicals applied to the processing bath. Therefore, it is exposed to high hardening temperature to obtain the desired content (please read the precautions on the back before filling this page)隼 (CNS) 8-4 specifications (210x297 public meals) Staff cooperation of Intellectual Property Bureau of the Ministry of Economic Affairs Du printed 46 1 927 A7 _ _ B7__ 5 2. Description of the invention (η) The correct amount of reactants in the textile can be confirmed before the level of treatment is required. The amount of textile obscenity before the application of the treatment chemical will dilute the "seen" of the textile after passing through the treatment bath The quantity of chemicals. The above-mentioned step, commonly known as the chemical aqueous solution of wet on wet application, can produce a strength higher than 13% compared to the application of chemicals to dry textiles. When treating wet For textiles, the shrinkage is better than for dry textiles. If the reaction mechanism is not discussed, one thing is certain: when the textiles have been pre-wetted, they can be completely wetted and saturated. All fibers can reach the same degree of saturation and swelling. It was found that dry textiles are not easily wetted uniformly when plugged with a chemically treated aqueous solution. In humidity-on-wet application, water and humectant are first applied and fully saturated before the application of the chemical aqueous solution. This is an example of a two stop continuous method of applying water and chemicals. Do not want to be limited by any theory, because this application should be distributed to areas without or less solution, if a textile has a point-like deeper wet area adjacent to the area that is not wet, then it is deeper wet The area contains more chemicals than it should. Areas with higher chemical concentrations will be treated more than adjacent areas with fewer chemicals. Therefore poor wetting or poor uniformity results in weak or over-treated micro areas and strong untreated areas in textiles. The textile strength is only as good as the weakest point. ° Now the observer is that textiles wetted to 50% with water before chemical application are quickly impregnated with twice the chemical concentration (for Twice the strength). When the chemical solution is used __: ___---- η -___ A paper size is applicable to the Chinese National Standard (CNS) A4 specification (21〇 × 2.97 mm) (Please read the precautions on the back before filling in this page)

461927 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(α) 在紡織品中的水稀釋至二分之一時’不但可達到正常的濃 度,而且該等化學品可在纖維之內外各處移動。其可確使 該處理化學品在紡織品中更均勻的施用。因此其並未存集 中的區域,每處均經相等的處理’因此該化學反應可得到 沒有微小-弱的點狀。 需注意者爲’當處理乾燥紡織品時’紡織品具有周圍 環境數量的濕度,爲了將於下文所述之理由僅使用一半數 量之甲醛。(預濕潤之紡織品已經含有水)°並不淸楚者爲 當施加混合物水溶液至乾燥紡織品時’一半的催化劑濃度 並未使用。此種理由極爲明顯。催化劑濃度依其自己的曲 線施用而不需精確地依甲醛而定。其水平迅速下降’因爲 如果使用於濕度在濕式處理的一半催化劑濃度使用於濕度 在乾燥處理,則催化劑量不足以得到良好的反應或良好的 處理。所使用的濃度係基於前案技藝中對乾燥紡織品所施 加之混合物水溶液。藉由參考早先的數據而選擇適當的催 化劑濃度,且依據數據中所示,雖然強度略低於濕度在濕 式處理但仍是相當接近。令人驚訝者爲在乾燥紡織品處理 的縮水性控制並不佳。如果催化劑濃度被減半,縮水性則 會更差。 尿素加至紡織品中造成在紡織品中所保留的強度顯著 增加。尿素可與其他化學品同時加至處理溶液中,或單獨 地或倂用地與選用成份依序加入。在一些加入尿素的試樣 中’其較之於使用未含有尿素於處理浴處理之試樣,在強 度上增高30%。尿素可加至處理水溶液組成物中以提供基 (請先閱讀背面之注意事項再填寫本頁) r 本紙银又度適用中國國家襟準(CNS ) A4規格(210X297公釐) 4 6 1927 A7 B7 五、發明説明(A ) 於紡織品重量之由0.5至3 %尿素,較佳爲1 一 2 % OWF, 或可能依序施加至達到在紡織品中的相同數量。 強度增加的機制仍未被了解,但是在機織紡織品和針 織品上其爲完全地可重現。尿素較佳爲在加至處理浴之則 先溶解於水中,且其係正好在任何濕潤劑加至處理浴之前 加入。上述中需注意者爲,濕潤劑亦可在預濕潤步驟中加 入。令人驚訝地者,使用尿素經處理的紡織品同時在抗張 強度與撕裂強度上至少增強30%。尿素的這個效應對於本 發明的水溶液系統爲特有的,因爲其對於其他的甲醛交聯 方法並無法增加強度。然而,其對於壓燙持久性’亦即DP 値,會略爲降低。對於該增強處理中在DP値上〇·5點的降 低但仍具有‘30%強度的增加並無太大關於。 因爲較佳爲使用尿素,與水溶液系統相容的尿素衍生 物的使用量可基於被加至該系統之尿素量而由熟於此藝者 輕易地決定。這些衍生物包括經取代的尿素’其中一或多 個有機基用於取代一或多個尿素的氫原子。此類有機基包 括低碳烷基’亦即甲基乙基,丙基,只要該等之尿素衍生 物的水溶解度在水溶液系統中沒有不利效應。同樣地’亦 可使用硫脲與其水可溶解衍生物。 可進一步發現,當尿素加至聚矽氧烷彈性體的水性乳 液中的濃度爲可形成可被儲存一長段時間的複合物時可得 到一種穩定的組成物,其可於使用時再稀釋。此可避免在 加入甲醛時分開加入尿素而形成施加至欲處理紡品之處理 浴。例如,甲醛,複合物和水可於適當比率下加至塡塞浴 . _______15_ 國國家標準(CNS ) Α4規格(210X297公釐) (請先閲讀背面之注意事項再填寫本頁) 訂 經 濟 部 智 慧 財 產 局 員 工 消 費 合 作 社 印 製 經濟部智慧財產局員工消費合作社印製 46 1927 A7 _B7__ 五、發明説明(A ) 中用於處理紡織品。其可使用好的泵出系統由儲存桶中泵 出而維持適當的比率,而且因此除去對於處理溶液槽的需 求。然而,甲醛或催化劑並不能加至合物內,因爲彈性體 ,尿素和甲醛或催化劑的組合並不足夠穩定地長期儲存。 處理水平大幅地依使用於處理溶液中的甲醛數量而定 ,但是也依所使用之催化劑數量而定。催化劑之加入應該 與甲醛成正比,例如愈多甲醛愈多催化劑等。尿素可能會 影嚮處理水平,但是其他成份,例如濕潤劑和其他的習用 選用成份對於處理水平並不影嚮。 所選擇的處理水平依紡織品而定,一些紡織品能抵抗 高的處理水平,但其他的則不能。下列所述者爲經驗法則 ,但實驗測試可顯示可使用何種處理。 其亦可能在甲醛的移除爲大得足以影嚮反應且提供不 充份的處理之前,使用可以使交聯反應產生的極高溫度。 依據本發明的此範圍,經塡塞的紡織品可立刻置於在大約 300至大約325°F的加熱室內。此爲本發明的極重要商業範 圍,因爲其足以在速度爲依紡織品和纖維種類而定的每分 鐘15-200碼商業規模下連續進行。較佳者爲此方法係爲商 業應用而設計,因此該方法需要具有商業價値。 該方法亦可在低溫度下使用反應性催化劑硬化及/或 存有彈性體來完成。其亦可使用在硬化期間可避免甲醛實 質損耗的任何技術組合。例如,低溫可與甲醛水溶液倂用 。其亦可能使用壓加大於大氣壓的加壓系統,藉此在甲醛 與被處理之含纖維素纖維之紡織品交聯之前可避免甲醛的 張尺度適用中酬家標準(CNS ) Μ規格(2丨〇><29;二釐〉 ~ (請先閲讀背面之注意事項再填寫本頁)461927 A7 B7 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs. 5. Description of the invention (α) When the water in the textile is diluted to half, not only can it reach a normal concentration, but these chemicals can be used inside and outside the fiber. Move around. It does allow a more uniform application of the treatment chemical in the textile. Therefore, it does not exist in the concentrated area, and each place is treated equally. Therefore, the chemical reaction can be obtained without micro-weak spots. It should be noted that 'when processing dry textiles' textiles have an amount of humidity in the surrounding environment, and for reasons described below, only half the amount of formaldehyde is used. (Pre-wet textiles already contain water) ° It is not surprising that when a mixture of aqueous solution is applied to dry textiles, one half of the catalyst concentration is not used. This reason is obvious. The catalyst concentration is applied on its own curve and does not need to depend on formaldehyde. Its level drops rapidly 'because if the catalyst concentration used for the humidity treatment in the wet process is half of the catalyst concentration used in the humidity treatment for the drying process, the amount of catalyst is not sufficient to obtain a good reaction or good treatment. The concentration used is based on a mixture of aqueous solutions applied to dry textiles in the prior art. The appropriate catalyst concentration was selected by referring to the previous data, and according to the data, although the intensity is slightly lower than the humidity in the wet treatment, it is still quite close. Surprisingly, the shrinkage control in dry textile processing is not good. If the catalyst concentration is halved, the shrinkage will be worse. The addition of urea to textiles results in a significant increase in the strength retained in the textiles. Urea can be added to the treatment solution at the same time as other chemicals, or separately or sequentially with selected ingredients. In some samples to which urea was added, it was 30% higher in strength than samples treated with a treatment bath that did not contain urea. Urea can be added to the composition of the treated aqueous solution to provide a base (please read the precautions on the back before filling this page) r The silver of this paper is also applicable to China National Standard (CNS) A4 (210X297 mm) 4 6 1927 A7 B7 5. Description of the invention (A) The weight of the textile is from 0.5 to 3% urea, preferably 1 to 2% OWF, or may be sequentially applied to reach the same amount in the textile. The mechanism of increased strength is still unknown, but it is completely reproducible on woven and knitted fabrics. Urea is preferably dissolved in water before being added to the treatment bath, and it is added just before any wetting agent is added to the treatment bath. Note that in the above, wetting agents can also be added in the pre-wetting step. Surprisingly, textiles treated with urea have at least a 30% increase in tensile and tear strength. This effect of urea is unique to the aqueous system of the present invention because it does not increase strength for other methods of cross-linking formaldehyde. However, it is slightly reduced for pressurization durability, i.e., DP 値. There is not much concern about the 0.5 point decrease in DP 値 in this enhancement process, but the increase with an intensity of '30%. Since urea is preferred, the amount of urea derivative compatible with the aqueous system can be easily determined by those skilled in the art based on the amount of urea added to the system. These derivatives include substituted urea 'in which one or more organic groups are used to replace one or more hydrogen atoms of urea. Such organic groups include lower alkyl groups, i.e. methylethyl, propyl, as long as the water solubility of these urea derivatives has no adverse effect in aqueous systems. Similarly, thiourea and its water-soluble derivative can also be used. It has further been found that when urea is added to the aqueous emulsion of polysiloxane elastomer at a concentration that can form a complex that can be stored for a long period of time, a stable composition can be obtained which can be diluted again at the time of use. This prevents the separate addition of urea when formaldehyde is added and forms a treatment bath that is applied to the textile to be treated. For example, formaldehyde, complexes and water can be added to the bath with the appropriate ratio. _______15_ National Standard (CNS) Α4 size (210X297 mm) (Please read the precautions on the back before filling this page) Order the wisdom of the Ministry of Economy Printed by the Consumer Cooperatives of the Property Bureau Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 46 1927 A7 _B7__ V. The invention description (A) is used to process textiles. It can be pumped from a storage tank using a good pumping system to maintain the proper ratio, and therefore removes the need for a processing solution tank. However, formaldehyde or catalyst cannot be added to the compound because the combination of elastomer, urea and formaldehyde or catalyst is not stable enough for long-term storage. The treatment level depends greatly on the amount of formaldehyde used in the treatment solution, but also on the amount of catalyst used. The addition of catalyst should be proportional to formaldehyde, such as more formaldehyde and more catalyst. Urea may affect treatment levels, but other ingredients, such as humectants and other commonly used ingredients, do not affect treatment levels. The level of treatment chosen depends on the textile. Some textiles can resist high levels of treatment, but others cannot. The following are rules of thumb, but experimental tests can show what treatments can be used. It is also possible to use extremely high temperatures that can cause the crosslinking reaction before the removal of formaldehyde is large enough to affect the reaction and provide inadequate processing. According to this range of the invention, the tamped textile can be immediately placed in a heating chamber at about 300 to about 325 ° F. This is an extremely important commercial area of the present invention because it is sufficient for continuous operation at a commercial scale of 15-200 yards per minute, depending on the type of textile and fiber. The preferred method is designed for commercial applications, so the method needs to have a commercial price. This method can also be accomplished at low temperatures using a reactive catalyst hardening and / or the presence of an elastomer. It can also use any combination of technologies that avoids the substantial loss of formaldehyde during hardening. For example, low temperature can be used with aqueous formaldehyde. It is also possible to use a pressurization system that is pressurized to greater than atmospheric pressure, thereby avoiding the formaldehyde application of formaldehyde before the cross-linking of the treated cellulose fiber-containing textiles with the CNS M standard (2 丨 〇 > <29; Erli> ~ (Please read the notes on the back before filling in this page)

461927 A7 B7 五、發明説明(β) 實質移除。 除此之外’當本發明的方法施用至含棉紡織品,包含 100%含棉紡織品’其比其他之習用方法使用更少的甲醛。 經本發明方法處理之襯衫衣料紡織品,其在處理後且汽蒸 定形該襯衫衣料之前含有大約6000 ppm,而相似的襯衫衣 料紡織品使用其他的交聯方法則爲700〇 ppm+。測試顯示, 連續運轉汽蒸定形室使經處理紡織品的曝露爲有效移除殘 餘之甲醛達濃度低至200 ppm。依消費者關切所購之物存有 甲醛的觀點而言,其亦爲本發明的一個重要範圍。其亦可 能使用連續或批次洗滌器淸洗紡織品。其均爲實質地移除 所有甲醛。 已知可加入足以形成軟式膜的聚合樹脂添加劑至紡織 品中。例如,此等添加劑可爲聚乙烯的膠乳或細微的水性 分散液,各種不同的丙烯酸烷酯聚合物,丙烯腈-丁二烯共 聚物,去乙醯化之乙烯-乙酸乙烯酯共聚物,聚胺基甲酸酯 和相似者。此等添加劑對熟於此藝者爲習知者,且一般爲 經濃縮水性膠乳形式之商用產品。此種膠乳在使用含催化 劑水溶液之塡塞浴處理之前經稀釋以提供大約1至3 %聚 合物固體。一種習知的軟化劑,其係爲使用樹脂處理或甲 醛交聯的壓烫持久性方法中所實質選擇的軟化劑,爲高密 度聚乙烯,Mykon HD。如同由實施例所示,非預期地發現 使用聚矽氧烷彈性體取代高密度聚乙烯可在淸洗後顯著地 減少經處理紡織品的撕裂強度損耗,同時對該方法提供更 好的控制。方法中良好控制的重要性對於有商業價値的方 (請先閱讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 、τ461927 A7 B7 5. Description of the invention (β) Substantially removed. In addition, when the method of the present invention is applied to a cotton-containing textile, which contains 100% cotton-containing textile, it uses less formaldehyde than other conventional methods. The shirt clothing textiles treated by the method of the present invention contain about 6000 ppm after treatment and before steaming to set the shirt clothing, while similar shirt clothing textiles use other crosslinking methods at 700 ppm +. Tests have shown that continuous operation of the steam setting chamber allows the exposure of the treated textiles to effectively remove residual formaldehyde down to 200 ppm. From the point of view of consumers concerned about the presence of formaldehyde in purchased products, it is also an important scope of the present invention. It is also possible to launder textiles using continuous or batch scrubbers. They all remove substantially all formaldehyde. It is known that a polymer resin additive sufficient to form a flexible film can be added to textiles. For example, these additives may be polyethylene latexes or fine aqueous dispersions, various alkyl acrylate polymers, acrylonitrile-butadiene copolymers, deacetylated ethylene-vinyl acetate copolymers, poly Carbamates and similar. These additives are known to those skilled in the art and are generally commercial products in the form of concentrated aqueous latex. This latex was diluted to provide approximately 1 to 3% polymer solids before being treated with a plug bath with a catalyst-containing aqueous solution. A conventional softener is a softener that is essentially selected in the method of pressing durability using resin treatment or formaldehyde crosslinking, and is a high-density polyethylene, Mykon HD. As shown by the examples, it was unexpectedly found that the use of polysiloxane elastomers instead of high density polyethylene can significantly reduce the tear strength loss of treated textiles after rinsing, while providing better control of the process. The importance of good control in the method For parties with commercial prices (please read the notes on the back before filling this page) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs, τ

本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 經濟部智慧財產局員工消費合作社印製 461927 A7 B7 五、發明説明(山) 法爲必要的,其可由持續運轉中提供〜致性的產品,且該 產品不受大氣壓’濕度和相似者的變化而受到不利的影嚮 0 因爲本發明方法可處理含纖維素纖維的紡織品,因此 亦可使用各種不同的天然纖維素妨織品和其混合物,例如 棉和黃麻。可使用於與-或多種上述之纖維素纖維混紡的 其他纖維例如爲聚醯胺(例如尼龍),聚酯,壓克力(例如 聚丙烯腈),聚嫌烴’和在反應溫度下穩定的任何纖維。此 類混紡物較佳包括棉或天然纖維素纖維爲至少35至40 m 量% ’最佳爲至少50至60重量%。螺縈和含螺縈之混紡 物亦包括在內。螺縈爲合成織物纖維的總稱,其主要成份 爲纖維素或其衍生物的其中一種。 紡織品可爲一種樹脂化物質且較佳爲未經樹脂化;其 可爲針織,機織,非機織,或其它構造。在加工之後,所 形成的抗,皺痕紡織品將會實質地在結織品壽命期間維持所 需的組態。除此之外,該紡織品即使在重複洗滌之後仍具 有極佳的淸洗外觀。 本發明並不依據所限定的溼度含量來控制交聯反應, 因爲該交聯反應在纖維素纖維的最高度溶脹狀態下爲最有 效。可使用較低的溼度量,但爲較差。 然而,當使用聚矽氧烷彈性體於該方法時,聚矽氧烷 彈性體需存在有足夠的數量以降低在紡織品中抗張強度和 撕裂強度的損耗,其通常與前案中使用例如Mykon HD的軟 化劑處理方法中處理相同紡織品合用。本發明配製物和方 —_______1« ____. 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁)This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 461927 A7 B7 5. The invention description (mountain) method is necessary and can be provided by continuous operation ~ And the product is unaffected by changes in atmospheric pressure, humidity and the like. Because the method of the present invention can treat textiles containing cellulose fibers, various natural cellulose fibers and fabrics can also be used. Mixtures such as cotton and jute. Other fibers that can be used for blending with-or more of the above-mentioned cellulose fibers are, for example, polyamide (e.g. nylon), polyester, acrylic (e.g. polyacrylonitrile), poly (hydrocarbons) and stable at reaction temperature Any fiber. Such blends preferably include cotton or natural cellulose fibers in an amount of at least 35 to 40 m%, most preferably at least 50 to 60% by weight. Spiral reeds and blends containing spiral reeds are also included. Snail is a general term for synthetic fabric fibers, and its main component is one of cellulose or its derivatives. The textile may be a resinated substance and preferably is unresinified; it may be knitted, woven, non-woven, or other construction. After processing, the resulting resistant, wrinkled textiles will substantially maintain the desired configuration during the life of the knotted fabric. In addition, the textile has an excellent scouring appearance even after repeated washing. The present invention does not control the cross-linking reaction based on the defined humidity content, because the cross-linking reaction is most effective in the most highly swelled state of cellulose fibers. A lower amount of humidity can be used, but it is worse. However, when a polysiloxane elastomer is used in this method, the polysiloxane elastomer needs to be present in a sufficient amount to reduce the loss of tensile strength and tear strength in the textile, which is usually the same as that used in the previous case. Mykon HD's softener treatment method is used in conjunction with the same textiles. Formulations and formulas of the present invention —_______ 1 «____. This paper size applies to China National Standard (CNS) A4 (210X297 mm) (Please read the precautions on the back before filling this page)

461927 A7 B7 五、發明説明(q) 法可調整至符合被處理紡織品之特定商用需求。例如,甲 酸和催化劑濃度可增加以提供更佳的處理;然後軟化劑濃 度也增加至可補償增加使用於該方法催化劑數量而造成之 撕裂強度損耗。其傾向於使用電腦化控制處理各種不同紡 織品的系統且容許處理不同紡織品時的變化,此爲本發明 方法的另一個優點。聚矽氧烷油狀物習用爲聚矽氧烷軟化 劑且經發現部份使用於紡織品處理,但其等強烈地趨向於 產生不同移除點狀而具有嚴重的缺點。然而,使用於本發 明方法的特定聚矽氧烷彈性體可完全克服這些問題。 欲使用本發明處理的混紡紡織品浸漬於一溶液以提供 一吸收爲基於紡織品重量(OWF)之約3 %甲醛,1 %催化劑 ,1 %聚矽氧烷樹脂彈性體。該步驟可依序完成或使用一 種溶液完成。當一次完成時,其需要之吸收爲大約66重量 %之配製物水溶液以達到上述之反應物在紡織品中之百分 率。然而,當處理100%含棉紡織品時,化學品濃度必須增 高使得5 %甲醛OWF,大約2 %催化劑和大約2 %彈性體塡 塞至紡織品內。這係與前案中處理100%棉的方法相反,前 案中因爲處理方法所致之強度損耗因而降低反應物濃度。 硬化溫度爲大約300°F。事實上,經塡塞的紡織品可置於 300°F之烤箱或加熱室。 甲醛濃度可改變,較佳係由熟於此藝者依據欲被處理 的紡織品判斷。該方法包括使用水溶液形式的甲醛且具有 之濃度爲含棉紡織品之〇.5重量%至10重量%。在紡織品 中較佳之甲醛濃度爲基於含棉紡織品重量之由1.5%至7 % (請先閲讀背面之注意事項再填寫本頁) ,βτ 經濟部智慧財產局員工消費合作杜印製 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 46 1927 A7 B7 五、發明説明(v《) 經濟部智慧財產局員工消費合作杜印製 含螺縈纖維之紡織品可使用混合物水溶液處理,該混 合物含有高濃度之甲醛’和足以催化甲醛和螺縈之間交聯 反應之催化劑,其中甲醛的濃度爲足以產生壓燙持久性紡 織品者,然後熱硬化該經處理紡織品以產生以水洗滌時實 質地不縮水的壓燙持久性螺縈紡織品。該方法亦可在混合 物水溶液中包括有效量的彈性體,特別爲聚矽氧烷彈性體 ,然後在存有催化劑和彈性體時甲醛與螺縈反應,且在甲 醛與螺縈反應之前甲醛不實質移除之條件下熱硬化該經處 理的含螺縈纖維紡織品’其用於改良紡織品的皺痕阻抵性 且降低撕裂和抗張強度的損耗。硬化溫度爲大約350卞。事 實上,經塡塞的紡織品可置於350°F之烤箱或加熱室。 甲醛濃度可改變,較佳係由熟於此藝者判斷。該方法 包括使用水溶液形式的甲醛且具有之濃度爲所處理含螺縈 紡織品之14重量%至20重量%。在螺縈紡織品中較佳之 甲醛濃度爲基於紡織品重量(OWF)之由15%至18%。 甲醛由經處理紡織品的移除爲本發明的進一步範圍, 其包含後來使用化學處理或淸洗步驟。這對於在工廠中的 商業加工爲有利的。經發現,在硬化後使用甲醛移除劑溶 液處理經整理的紡織品可使紡織品具有可接受的甲醛水平 ,該甲醛移除劑例如爲有機酸,如草酸,甲酸或相似者。 在處理水溶液中的酸濃度可依例行的實驗來決定,其明顯 地依據使用於該方法的甲醛濃度而定。酸濃度的改變爲在 處理溶液中由大約0.5重量%至大約3重量%。 (請先閱讀背面之注意事項再填寫本頁)461927 A7 B7 V. Description of Invention (q) The method can be adjusted to meet the specific commercial needs of the textiles being processed. For example, formic acid and catalyst concentrations can be increased to provide better handling; then the softener concentration is also increased to compensate for the loss of tear strength caused by increasing the amount of catalyst used in the process. It tends to use a computerized control system for processing a variety of different textiles and tolerates variations when processing different textiles, which is another advantage of the method of the present invention. Polysiloxane oils are conventionally used as polysiloxane softeners and have been found to be partially used in textile treatment, but they strongly tend to produce different removal points and have serious disadvantages. However, the specific silicone elastomers used in the method of the present invention can completely overcome these problems. The blended textiles to be treated with the present invention are impregnated in a solution to provide an absorption of about 3% formaldehyde, 1% catalyst, and 1% polysiloxane resin elastomer based on the weight of the textile (OWF). This step can be done sequentially or using a solution. When completed in one shot, it requires an absorption of about 66% by weight of the aqueous formulation solution to achieve the above-mentioned percentage of the reactant in the textile. However, when processing 100% cotton-containing textiles, the chemical concentration must be increased such that 5% formaldehyde OWF, approximately 2% catalyst, and approximately 2% elastomer are trapped in the textile. This is in contrast to the method used to treat 100% cotton in the previous case, which reduced the reactant concentration due to the strength loss caused by the treatment method. The hardening temperature is approximately 300 ° F. In fact, chopped textiles can be placed in an oven or heating chamber at 300 ° F. The formaldehyde concentration can be changed, and it is best judged by the artist based on the textiles to be treated. The method includes using formaldehyde in the form of an aqueous solution and having a concentration of 0.5 to 10% by weight of the cotton-containing textile. The preferred formaldehyde concentration in textiles is from 1.5% to 7% based on the weight of cotton-containing textiles (please read the precautions on the back before filling out this page), βτ Intellectual Property Bureau of the Ministry of Economic Affairs, consumer cooperation, printed paper standards apply China National Standard (CNS) A4 specification (210X297 mm) 46 1927 A7 B7 V. Description of invention (v ") The consumer cooperation of the Intellectual Property Bureau of the Ministry of Economic Affairs Du printed textiles containing snail fiber can be treated with an aqueous solution of the mixture. The mixture Contains a high concentration of formaldehyde 'and a catalyst sufficient to catalyze the cross-linking reaction between formaldehyde and snails, where the concentration of formaldehyde is sufficient to produce a stamped durable textile, and then heat-treating the treated textile to produce a substantial amount when washed with water Non-shrinkable permanent snail fabric. This method can also include an effective amount of an elastomer, especially a polysiloxane elastomer, in an aqueous solution of the mixture, and then formaldehyde reacts with snails in the presence of a catalyst and elastomer, and the formaldehyde is not substantial before the reaction of formaldehyde and snails The treated snail-containing fiber textile is thermally hardened under the conditions of removal, which is used to improve the wrinkle resistance of the textile and reduce the tear and loss of tensile strength. The hardening temperature is about 350 ° F. In fact, choked textiles can be placed in an oven or heating chamber at 350 ° F. The formaldehyde concentration can be changed, and it is better to be judged by those skilled in the art. The method includes using formaldehyde in the form of an aqueous solution and having a concentration of 14% to 20% by weight of the treated snail-containing textile. The preferred formaldehyde concentration in snail fabric is from 15% to 18% based on the weight of the textile (OWF). Removal of formaldehyde from treated textiles is a further scope of the present invention, which involves the subsequent use of chemical treatment or washing steps. This is advantageous for commercial processing in factories. It has been found that treating finished textiles with a formaldehyde remover solution after hardening allows the textiles to have acceptable formaldehyde levels, such as organic acids such as oxalic acid, formic acid or the like. The acid concentration in the treated aqueous solution can be determined by routine experimentation, which obviously depends on the formaldehyde concentration used in the method. The change in acid concentration was from about 0.5% to about 3% by weight in the treatment solution. (Please read the notes 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) 461927 A7 B7 五、發明説明(\°\ ) 對於處理蛋白質纖維,例如絲或羊毛,則需要較高的 甲醛濃度。如同於前文中所述者,聚矽氧烷彈性體與蛋白 質纖維反應。經年以來,甲醛被使用於羊毛,但並不用爲 產生壓烫持久性性質。如果羊毛纖維如同在文獻中所建議 地使用基於物品重量之4.0%甲醛處理,則天然羊毛的交聯 物增強,因此使羊毛對於鹼降解具有阻抗性。亦即羊毛顯 示出降低的縮水性。 然而’如果在本發明方法中羊毛之處理係使用極高濃 度之甲醛,及催化劑,較佳爲反應性催化劑,則經本發明 方法處理之毛類紡織品可得到相當高的壓燙持久性(Dp)。 因爲相對表面纖維的咬合使纖維只能在一個方向移動,因 此對於羊毛通遍有機械縮水性,更而阻礙羊毛的壓烫持久 性(DP)性質。甲醛與羊毛纖維的交聯並不強到可以克服 由於熱’水和可打開纖維的淸潔劑所引致的機械縮水性。 經發現’在使用甲醛處理之前已經防縮水之羊毛紡織品( 氯化作用,以過錳酸鉀,或過氧化氫處理),在14〇卞的家 用洗衣機中水洗後顯示出具有極佳的DP。 比引用文獻所使用者更高的甲醛濃度係相似於在處理 螺縈時所使用者,例如基於紡織品重量的16%甲醛,和 4.5%催化劑LF。亦使用一般的軟化劑。 這些處理對於不具有防縮水的羊毛有效,但是對於超 過一或二次淸洗而開始產生縮絨縮水性(felting shrinkage)(機械性)時並不具效果。因爲縮絨縮水性增 加時,DP即消失。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐〉 (請先閱讀背面之注意事項再填寫本頁) --5 經濟部智慧財產局員工硝費合作社印製 461927 A7 _^____B7 _.__This paper size applies to Chinese National Standard (CNS) A4 (210X297 mm) 461927 A7 B7 V. Description of the invention (\ ° \) For the treatment of protein fibers, such as silk or wool, a higher formaldehyde concentration is required. As described earlier, polysiloxane elastomers react with protein fibers. Formaldehyde has been used on wool for many years, but it is not used to produce permanent properties. If wool fibers are treated with 4.0% formaldehyde based on the weight of the article as suggested in the literature, the cross-linking of natural wool is enhanced, thus making the wool resistant to alkaline degradation. That is, wool shows reduced shrinkage. However, if the wool treatment in the method of the present invention uses a very high concentration of formaldehyde and a catalyst, preferably a reactive catalyst, the wool textile treated by the method of the present invention can obtain a relatively high press durability (Dp) . Because the fibers on the opposite surface can only move the fiber in one direction, it has mechanical shrinkage for the wool throughout, and hinders the wool's permanence (DP) properties. The cross-linking of formaldehyde with wool fibers is not strong enough to overcome the mechanical water shrinkage caused by hot ' water and fiber opener detergents. It was found that wool textiles that had been shrink-proofed before being treated with formaldehyde (chlorination, treated with potassium permanganate, or hydrogen peroxide), showed excellent DP after being washed in a domestic washing machine at 140 ° F. Higher formaldehyde concentrations than those cited in the literature are similar to those used when treating snails, such as 16% formaldehyde based on textile weight, and 4.5% catalyst LF. General softeners are also used. These treatments are effective for wools that do not have shrinkage resistance, but they are not effective when starting to produce shrinking shrinkage (mechanical) after one or two washings. This is because the DP disappears as the shrinkage increases. This paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) (Please read the notes on the back before filling this page) --5 Printed by the Intellectual Property Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 461927 A7 _ ^ ____ B7 _ .__

五、發明説明(yO (請先閲讀背面之注意事項再填寫本頁) 絲在化學性質上與羊毛相似,但是在物理性質上極不 同,其以一種極巧妙的方法進行部份穩定。當使用與羊毛 所使用的相同濃度時,相較於未經處理的控制組,其在外 觀上顯示出更光滑更新,且較少的細縐痕。當絲經由本發 明方法處理後,經過淸洗後仍高度地維持絲纖維的光澤或 閃亮。 使用於本方法的催化劑包括氟矽酸,其可使用於溫和 反應且可施用至混紡紡織品。在高度施用上,對於純棉紡 織品,或襯衫衣料紡織品可使用的催化劑例如爲氯化鎂摻 加檸檬酸,其爲一種商用的催化劑Freecat 9號且係與含 有氯化鋁/鎂的催化劑相似。可使用於本發明的一個種類 催化劑包括述於美國專利權3,960,482號者,其中的全部 揭示被倂於本文用爲參考。這些催化劑包括含有酸鹽的酸 催化劑,該等酸鹽例如爲銨,鎂,鋅,鋁和鹼土金屬氯化 物,硝酸鹽,溴化物,二氟化物,硫酸鹽,磷酸鹽,和氟 硼酸鹽。亦可使用氯化鎂,氯氫氧化鋁和銷,及其等之混 合物8 經濟部智慧財產局員工消費合作杜印製 亦可使用於本發明中做爲催化劑之水溶性酸’其同時 包括無機酸和有機酸,例如胺基磺酸,磷酸,鹽酸,硫酸 ,己二酸,反丁烯二酸,檸檬酸,酒石酸和相似。該等催 化劑可依熟於此藝者簡易的判定而單獨或組合使用。 在高度施用上,對於純螺縈紡織品,或襯衫衣料紡織 品可使用的催化劑例如爲氯化鎂摻加檸檬酸,其係爲一種 商用的催化劑,Freecat LF。Freecat 9號係爲另一種氯化 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 461927 A7 B7 五、發明説明(,) 鎂催化劑,其含有氯化鋁/鎂。這些催化劑可得自Freedom Text i le化學品公司。 (請先閲讀背面之注意事項再填寫本頁) 催化劑LF爲一種使用於棉之習用甲醛處理方法的特 別反應性或『熱門』的氯化鎂催化劑’且其含有氯化鎂鹽 和可促進酸性之有機酸,例如檸檬酸推進酸度。亦可使用 其他的酸。催化劑LF被硏發用於硬化不易反應之低甲醛 樹脂。奇妙者爲,一般人會因爲其比催化劑9號(僅有氯 化鎂)更具有酸性,因此預期其會引起較大的損害和較多 強度損耗。事實上並非如此,此種催化劑更常產生較佳的 處理和較佳的強度。 經濟部智慧財產局員工消費合作社印製 在硬化步驟的交聯反應期間,當交聯作用產生時濕度 由紡織品中生成,造成紡織品溼度含量的降低。在紡織品 具有溼度含量爲20%或更低時,傾向於使交聯反應的效率 降低而需要更高的甲醛濃度。在本發明的一個較佳範圍中 ,溼度昇高至高水平,亦即大於20%,較佳爲大於30%, 例如由60-100%或更多,則交聯作用爲最佳化。溼度極不 易控制,但並不造成本發明的困擾。當然,並不允許水過 量存在而造成催化劑轉移至紡織品。 在下列實施例所示的結果係依據下列的標準方法得到 • . 1 ·經家庭的重複淸洗後紡織品的外觀:AATCC測試 方法 124-1992 2 .抗張強度:ASTM :測試方法D-1682-64(測試1C) 3 .撕裂強度·· ASTM :測試方法D-1424-83落體擺錘 _;_91 本紙張尺度適用中國國家標準(CNS) A4規格(210X297公釐) 461927 A7 B7 五、發明説明(,) 方法 4 ·縮水性:AATCC測試方法150_1995 5 ·紡織品皺痕恢復:角度回復方法:ΑΑΤ(χ測試方 法66-1990侍到角度旋轉及AATCC測試方法143-1492提供 DP値。 在測定紡織品的DP値時,視覺比較測試之進行係在 控制光源條件下經處理紡織品中的皺痕數量與預先製成鈹 痕的塑膠複製品上存在之皺痕數量相比較。那些塑膠複製 品具有不同程度的皴痕且範圍由極皺的結織品爲1 DP數値 至平滑無皴痕結織品的5.0 DP·。DP數値愈高愈佳。對於市 場上可接受的無雛痕紡織品,需要有DP數値爲3.5,但極 少達到。熟於此藝者認爲DP爲3.50與3.25時兩者差異最 大。在DP爲3.50時,所有的皺痕變平且消失。在dp爲 3.25時,仍可見到所有皴痕並且顯示出銳利的摺痕。對於 棉紡織品,市場上可接受的目標爲DP 3.0,同時底紗 (filling)抗張強度爲25膀及底紗撕裂強度爲24盘司。( 在本發明之前並未有螺縈的DP,因爲其係使用甲醛DP方法 處理)。與這些性質相同重要甚或更重要者爲該方法必須在 工業規模時具有可重現性。 更甚者,縮水性控制爲非常重要的性質,且對於經處 理棉而言爲無法接受的DP値對於螺縈而言變得可接受,其 可使縮水性受到控制。在含螺縈纖維中所得到之縮水性控 制係藉由使用一混合物水溶液,含有高濃度甲醛,及足以 催化甲醛與螺縈交聯反應之催化劑,處理含螺縈纖維之紡 — — _ 74______ ______ _______ 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閲讀背面之注意事項再填寫本頁) 訂 經濟部智慧財產局員工消費合作杜印製 經濟部智慧財產局員工消費合作社印製 461927 A7 _____ B7 五、發明説明(A) 織品且其中甲醛的濃度爲足以產生紡織品的縮水性控制, 及熱硬化經處理紡織品以生成在水洗時實質地不縮水的經 處理螺縈紡織品。 在下列的所有實施例中,如同於本技藝中習用者,非 離子性濕潤劑亦被使用。濕潤劑之使用量爲大約0.1重量 %。使用於棉實施例之濕潤劑爲烷基芳基聚醚醇,例如三 硝基甲苯(Triton) X-100。使用於螺縈實施例之濕潤劑爲 三甲基王醇乙氧棊化物,例如聯合碳化物次十四烷基硫酸 鈉(Union Carbide Tergitol) TMNG。濕潤劑之使用可藉由 纖維之處理水溶液使紡織品完全濕潤。 純棉紡織品最難處理,因爲該處理方法會造成抗張強 度和撕裂強度的嚴重損耗。此種抗張強度和撕裂強度的嚴 重損耗造成經處理紡織品無法被市場所接受。對於純棉襯 衫衣料妨織品的抗張強度和撕裂強度的一般工業標準爲具 有底紗抗張強度爲25磅及底紗撕裂強度爲24盎司。棉紡 織品必須符合及/或超過此標準。測試條件示於表中。 在含棉紡織品的一些測試中,聚矽氧烷彈性體爲商用 的軟化劑西格菲(Sedgefield)弾性體軟化劑ELS,其被加入 做爲不透明的白色液體且含有24-26%聚矽氧烷,其具有酸 鹼値爲5.0-7.0及易以水稀釋。當使用於本發明時,該產 物使用Mykon HD且催化劑濃度爲0.8%時生成DP値,在1 次淸洗後得到DP値3.5 ’及5次淸洗後爲3.25所需之催化 劑濃度爲2.0%。 另一種可被使用之聚矽氧烷彈性體爲商用的二甲基聚 尺度適用中國國家標準(CNS ) A4規格(210X29^·^ ' (請先閱讀背面之注意事項再填寫本頁) 訂 經濟部智慧財產局員工消費合作社印製 461927 A7 B7 五、發明説明(外) 矽氧烷乳液,其由General Electric所售且使用之產品號 爲SM2112。該物質被加入做爲不透明的白色液體且含有 24-26%聚矽氧烷彈性體,其具有酸鹼値爲5.0-8.0及易以 水稀釋。 使用Mykon HD且催化劑濃度爲0.8%時,其抗張強度 和撕裂強度爲顯著且非預期地高於催化劑濃度爲2.0%者且 得到相同的DP結果。催化劑濃度爲1.0% ELS被推薦使用 以確使安全性範圍,因此處理間所有的任何變化將會在可 接受的規格內。 甲醛係爲水溶液形式,其係製備自含有37%甲醛水溶 液之商用福爾馬林(Formalin)。 如同於本技藝中所習用者,於實施例和表中所示的所 有百分率係基於由製造商中所收到之產物或化學品。百分 率爲重量百分率,且於大部份之情形下爲基於被處理之紡 織品重量,除了所加入之濕潤劑爲基於欲加入之浴器的重 量百分率。下列所示之實施例係用於說明且對本發明提供 更佳理解性而非限制之用。 紡織品由浴器中吸收處理溶液數量之決定係由紡織品 通經僅含水之塡塞浴後再經過擠壓滾筒。乾燥紡織品之特 定重量被決定,且與通經塡塞浴和擠壓滾筒後之相同量紡 織品比較。吸收量係以吸收百分率表示。例如,90%之吸 收意爲該紡織品在通經塡塞浴和擠壓滾筒後吸收90%之原 重量。顯然地,吸收量係依紡織品多快速地移經浴器,及 滾筒之間的捏夾壓力’及紡織品濕潤的傾向而定。這些參 _ ___:-26________ 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁) 訂 五、發明説明(X) (請先閲讀背面之注意事項再填寫本頁) 數可被調整來控制吸收量’因此可控制化學品在塡塞浴中 之濃度進一步控制基於紡織品重量的化學品百分率。這些 調整的技術爲本技藝中所習知者,且對於熟於此藝者必需 知道吸收量使得可以測定基於紡織品重量(OWF)之化學品 重量,藉此控制紡織品之反應以得到所需的結果。 下列所示之實施例係用於說明且對本發明提供更佳理 解性而非限制之用。爲了確定甲醛在習用方法中失去的事 實,實驗將進行於如同在習用方法中令紡織品在極熱的空 氣中迅速加熱,及依據本發明方法加熱。 實施例1 經濟部智慧財產局員工消費合作社印製 如同所述者,其可能在足量甲醛喪失良好的處理之前 ,使用高至可達到交聯反應之溫度硬化。在此實驗中’ 100 %純棉牛津襯衫衣料使用濃度爲5.0% OWF之甲醛(37% ),0.8% 0WF之由Freedom Textile化學品公司所製之促 進劑Freecat 9號,和1.5% 0WF之由西格菲特用品公司 (Sedgefields Specialties)製造之聚砂氧院彈性體軟化劑 ,Sedgesoft ELS,塡塞至吸收大約60-70%。該樣品然後 乾燥且在拉伸下於設定在300°f之空氣循環烤箱中硬化10 分鐘。 實施例2 ' 在實施例1所使用相同紡織品,取另一個樣品使用相 似的溶液塡塞,僅有之不同爲做爲催化劑的加速劑9號爲 1.0% 0WF。否則樣品以完全相同的方式處理。 實施例3 __ —--^22--—--— 本紙張尺度適用中國國家楼準(CNS ) A4规格(21 〇 X 297公釐) d6 1 927 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(Λ) 在實施例1所使用相同紡織品,取另一個樣品使用相 似的溶液塡塞,僅有之不同爲做爲催化劑的加速劑9號爲 2.0% OWF。否則樣品以完全相同的方式處理。 實施例4 在實施例1所使用相同紡織品,取另一個樣品使用相 似的溶液塡塞,僅有之不同爲做爲催化劑的加速劑9號爲 0.4% OWF,及 Mykon HD 用來取代 Sedgesoft ELS 彈性體 軟化劑。否則樣品以完全相伺的方式處理。 實施例5 在實施例1所使用相同紡織品,取另一個樣品使用相 似的溶液塡塞,僅有之不同爲做爲催化劑的加速劑9號爲 0.8% 0WF,及 Mykon HD 用來取代 Sedgesoft ELS 彈性體 軟化劑。否則樣品以完全相同的方式處理。 實施例Θ 在實施例1所使用相同紡織品,取另一個樣品使用相 似的溶液塡塞,僅有之不同爲做爲催化劑的加速劑9號爲 1.0% 0WF,及 Mykon HD 用來取代 sedgesoft ELS 彈性體 軟化劑。否則樣品以完全相同的方式處理。 實施例7 在實施例1所使用相同紡織品,取另一個樣品使用相 似的溶液塡塞,僅有之不同爲做爲催化劑的加速劑9號爲 1.5% 0WF,及 Mykon HD 用來取代 Sedgesoft Els 彈性體 軟化劑。否則樣品以完全相同的方式處理。 實施例8 (請先閲讀背面之注意事項再填寫本頁)V. Description of the invention (yO (please read the notes on the back before filling out this page) Silk is similar to wool in chemical properties, but very different in physical properties. It is partially stabilized in a very clever way. When used At the same concentration as used for wool, compared with the untreated control group, it shows a smoother and newer appearance and fewer fine crease marks. When the silk is treated by the method of the present invention, it is washed after washing Still highly maintains the luster or shine of silk fibers. Catalysts used in the process include fluorosilicic acid, which can be used for mild reactions and can be applied to blended textiles. On high applications, for cotton textiles, or shirting textiles Catalysts that can be used are, for example, magnesium chloride with citric acid, which is a commercial catalyst Freecat 9 and is similar to catalysts containing aluminum chloride / magnesium. One type of catalyst that can be used in the present invention includes those described in US Patent 3,960,482 No., all of which is incorporated herein by reference. These catalysts include acid catalysts containing acid salts, examples of such acid salts For ammonium, magnesium, zinc, aluminum and alkaline earth metal chlorides, nitrates, bromides, difluorides, sulfates, phosphates, and fluoroborates. Magnesium chloride, aluminum chlorohydrochloride, and pins are also used, among others Mixture 8 Consumption cooperation by employees of the Intellectual Property Bureau of the Ministry of Economic Affairs can be used in the present invention as a water-soluble acid as a catalyst. It also includes inorganic and organic acids, such as aminosulfonic acid, phosphoric acid, hydrochloric acid, sulfuric acid, Adipic acid, fumaric acid, citric acid, tartaric acid, and the like. These catalysts can be used alone or in combination according to the simple judgment of the artist. For high application, for pure snail fabrics, or shirting materials The catalyst that can be used in textiles is, for example, magnesium chloride with citric acid, which is a commercially available catalyst, Freecat LF. Freecat 9 is another chlorinated paper. The paper size is applicable to Chinese National Standard (CNS) A4 (210X297 mm) 461927 A7 B7 V. Description of the invention (,) Magnesium catalyst, which contains aluminum / magnesium chloride. These catalysts are available from Freedom Text Chemical Co. (Please read the back first) Note: Please fill in this page again.) The catalyst LF is a special reactive or "popular" magnesium chloride catalyst used in cotton's conventional formaldehyde treatment method, and it contains magnesium chloride and organic acids that promote acidity, such as citric acid to promote acidity. .Other acids can also be used. Catalyst LF is used to harden low-formaldehyde resins that are difficult to react. The wonderful thing is that most people will be more acidic than Catalyst 9 (only magnesium chloride), so it is expected to cause Large damage and more strength loss. In fact this is not the case, such catalysts often produce better handling and better strength. The Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs prints during the crosslinking reaction during the hardening step, when When cross-linking occurs, the humidity is generated in the textile, resulting in a decrease in the moisture content of the textile. When the textile has a moisture content of 20% or less, it tends to reduce the efficiency of the crosslinking reaction and requires a higher formaldehyde concentration. In a preferred range of the present invention, when the humidity rises to a high level, that is, greater than 20%, preferably greater than 30%, for example from 60 to 100% or more, the crosslinking effect is optimized. Humidity is extremely difficult to control, but does not cause a problem for the present invention. Of course, excessive amounts of water are not allowed to cause catalyst transfer to textiles. The results shown in the following examples are obtained in accordance with the following standard methods: 1. Appearance of textiles after repeated laundering at home: AATCC test method 124-1992 2. Tensile strength: ASTM: Test method D-1682- 64 (Test 1C) 3. Tear strength · ASTM: Test method D-1424-83 falling body pendulum _; _91 This paper size applies to China National Standard (CNS) A4 specification (210X297 mm) 461927 A7 B7 V. Invention Explanation (,) Method 4 · Shrinkage: AATCC test method 150_1995 5 · Textile wrinkle recovery: Angle recovery method: AAT (χ test method 66-1990 wait angle rotation and AATCC test method 143-1492 provide DP 値. In the case of DP of textiles, the visual comparison test is performed under the control of the light source. The number of wrinkles in treated textiles is compared with the number of wrinkles on plastic replicas made of beryllium scars. Those plastic replicas have different The degree of creases and the range from extremely wrinkled knotted fabric is 1 DP number to 5.0 DP · smooth smooth creaseless knotted fabric. The higher the DP number, the better. For the market-acceptable no-smear textiles, DP値 is 3.5, but rarely reached. Those who are familiar with this art think that the difference between the two is the biggest when DP is 3.50 and 3.25. When DP is 3.50, all wrinkles flatten and disappear. When dp is 3.25, it can still be seen All creases and sharp creases are shown. For cotton textiles, the acceptable target on the market is DP 3.0, with a filling tensile strength of 25 and a base yarn tear strength of 24 pans. There is no DP for snails before this invention, because it is treated with formaldehyde DP method. As important as these properties, or even more important, is that the method must be reproducible on an industrial scale. Furthermore, shrinkage Control is a very important property, and DP 値, which is unacceptable for treated cotton, becomes acceptable for snails, which can control the shrinkage. Control of shrinkage in snail-containing fibers By using a mixture of aqueous solution containing high concentration of formaldehyde, and a catalyst sufficient to catalyze the cross-linking reaction of formaldehyde and snail, the spinning of snail-containing fiber is treated with _ 74______ ______ _______ This paper size applies to Chinese national standards (CNS) A4 specification (210X297 mm) (Please read the notes on the back before filling out this page) Order the consumer cooperation of the Intellectual Property Bureau of the Ministry of Economic Affairs Du printed by the Intellectual Property Bureau of the Ministry of Economic Affairs and the Consumer Cooperative printed by 461927 A7 _____ B7 5 2. Description of the invention (A) Fabrics in which the concentration of formaldehyde is sufficient to produce a shrinkage control of the textiles, and the treated textiles are thermally hardened to produce treated snail fabrics that do not substantially shrink when washed. In all of the following examples, non-ionic humectants are used, as are those skilled in the art. The amount of humectant used is about 0.1% by weight. The humectant used in the cotton examples is an alkylaryl polyether alcohol, such as Triton X-100. The humectant used in the examples of snails is trimethyl acetohydrin ethoxylate, such as Union Carbide Tergitol TMNG. The use of humectants can completely wet the textiles with the aqueous solution of the fibers. Cotton textiles are the most difficult to handle because they can cause severe loss of tensile and tear strength. This severe loss of tensile and tear strength renders treated textiles unacceptable on the market. The general industry standards for cotton undershirt fabrics may have a tensile strength and tear strength of the fabric with a base yarn tensile strength of 25 pounds and a base yarn tear strength of 24 ounces. Cotton fabrics must meet and / or exceed this standard. The test conditions are shown in the table. In some tests of cotton-containing textiles, the polysiloxane elastomer was a commercial softener Sedgefield softener ELS, which was added as an opaque white liquid and contained 24-26% polysiloxane Alkane, which has an acid-base ratio of 5.0-7.0 and is easily diluted with water. When used in the present invention, the product uses Mykon HD and DP 値 is formed at a catalyst concentration of 0.8%. DP 値 3.5 'is obtained after 1 wash, and 3.25 is obtained after 5 washs. The required catalyst concentration is 2.0%. . Another type of polysiloxane elastomer that can be used is a commercial dimethyl polymer standard that applies the Chinese National Standard (CNS) A4 specification (210X29 ^ · ^ '(Please read the precautions on the back before filling this page). Ordering economy Printed by the Intellectual Property Cooperative of the Ministry of Intellectual Property, 461927 A7 B7 V. Description of the Invention (outside) Siloxane emulsion, which is sold and used by General Electric under the product number SM2112. This substance is added as an opaque white liquid and contains 24-26% polysiloxane elastomer, which has a pH of 5.0-8.0 and is easily diluted with water. When Mykon HD is used and the catalyst concentration is 0.8%, its tensile strength and tear strength are significant and unexpected. Above the catalyst concentration of 2.0% and get the same DP result. The catalyst concentration of 1.0% ELS is recommended to ensure the safety range, so any changes between treatments will be within acceptable specifications. Formaldehyde In the form of an aqueous solution, it is prepared from commercial Formalin containing a 37% formaldehyde aqueous solution. As used in the art, all percentages shown in the examples and tables are based on Products or chemicals received by the manufacturer. Percentages are weight percentages, and in most cases are based on the weight of the textile being treated, except that the wetting agent added is based on the weight percentage of the bath to be added. The examples shown below are intended to illustrate and provide better understanding of the present invention and are not intended to be limiting. The determination of the amount of textile processing solution absorbed in the bath is determined by passing the textile through a bath containing only water and then extruding it. Drum. The specific weight of the dry textile is determined and compared with the same amount of textile after passing through the bath and pressing the drum. The absorption is expressed as a percentage of absorption. For example, 90% absorption means that the textile is passing through the fabric. After plugging the bath and squeezing the roller, it absorbs 90% of the original weight. Obviously, the amount of absorption depends on how quickly the textile moves through the bath, the pinch pressure between the rollers, and the tendency of the textile to wet. These parameters_ ___ :-26________ This paper size is applicable to China National Standard (CNS) A4 specification (210X297 mm) (Please read the precautions on the back before filling this page). Note (X) (Please read the notes on the back before filling this page) The number can be adjusted to control the amount of absorption ', so the concentration of chemicals in the bath can be controlled to further control the percentage of chemicals based on the weight of the textile. These adjustments The technology is known to those skilled in the art, and for those skilled in the art, it is necessary to know the absorption amount so that the weight of the chemical based on the weight of the textile (OWF) can be measured, thereby controlling the reaction of the textile to obtain the desired result. The examples shown are for illustration and to provide a better understanding of the invention rather than limiting. In order to determine the fact that formaldehyde is lost in conventional methods, experiments will be performed as in conventional methods that expose textiles to extremely hot air Rapid heating, and heating according to the method of the present invention. Example 1 Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs As mentioned, it may be hardened at a temperature as high as the crosslinking reaction can be achieved before a sufficient amount of formaldehyde is lost to good treatment. In this experiment, '100% cotton Oxford shirt fabric uses 5.0% OWF formaldehyde (37%), 0.8% 0WF, Freecat No. 9 accelerator produced by Freedom Textile Chemical Company, and 1.5% 0WF. Sedgesoft ELS, an elastomer softener made by Sedgefields Specialties, is squeezed to absorb about 60-70%. The sample was then dried and hardened under stretching in an air circulating oven set at 300 ° f for 10 minutes. Example 2 'The same textile was used in Example 1, and another sample was taken and plugged with a similar solution. The only difference was that the accelerator No. 9 as the catalyst was 1.0% 0WF. Otherwise the sample is processed in exactly the same way. Example 3 __ ----- ^ 22 ------ This paper size is applicable to China National Building Standard (CNS) A4 (21 × 297 mm) d6 1 927 A7 B7 Printed by the Consumer Cooperative of Intellectual Property Bureau of the Ministry of Economic Affairs Preparation 5. Description of the Invention (Λ) The same textile was used in Example 1, and another sample was taken and plugged with a similar solution. The only difference was that the accelerator No. 9 as the catalyst was 2.0% OWF. Otherwise the sample is processed in exactly the same way. Example 4 The same textile was used in Example 1, and another sample was used to plug the solution. The only difference was that the accelerator No. 9 was 0.4% OWF, and Mykon HD was used instead of Sedgesoft ELS. Body softener. Otherwise, the samples are processed in a completely similar manner. Example 5 The same textile was used in Example 1, and another sample was used to plug the solution with a similar solution. The only difference was that the accelerator No. 9 was 0.8% 0WF, and Mykon HD was used instead of Sedgesoft ELS. Body softener. Otherwise the sample is processed in exactly the same way. Example Θ The same textile was used in Example 1. Another sample was taken with a similar solution for plugging. The only difference was that the accelerator No. 9 as the catalyst was 1.0% 0WF, and Mykon HD was used to replace sedgesoft ELS elasticity. Body softener. Otherwise the sample is processed in exactly the same way. Example 7 The same textile was used in Example 1. Another sample was used to plug the solution with a similar solution. The only difference was that the accelerator No. 9 as a catalyst was 1.5% 0WF, and Mykon HD was used instead of Sedgesoft Els. Body softener. Otherwise the sample is processed in exactly the same way. Example 8 (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) 4 6 1 9 2 7 Α7 Β7 五、發明説明(VI ) (請先閱讀背面之注意事項再填寫本頁) 在實施例1所使用相同紡織品,取另一個樣品使用相 似的溶液塡塞,僅有之不同爲做爲催化劑的加速劑g號爲 2.0% OWF,及 Mykon HD 用來取代 Sedgesoft ELS 彈性體 軟化劑。否則樣品以完全相同的方式處理。 實施例9 相同紡織品的樣品在家用洗衣機中淸洗且脫水,但是 不使用任何的交聯方法處理。 實施例10 相同紡織品的另一個樣品被用爲未經處理,未經淸洗 的控制組。 於表I中可淸楚得知,經彈性體軟化劑處理的樣品, 較之於使用Mykon HD處理之任何樣品可得到較高程度之壓 燙持久性。對於每種處理,抗張強度與縮水性爲相似。 經濟部智慧財產局員工消費合作社印製 在另一個實驗中,其結果示於表Π,100%棉牛津襯衫 衣料的樣品使用甲醛爲3.0和5.0% 0WF的兩種濃度塡塞 ,每種濃度亦使用0.8,1.0和2.0%的三種濃度加速劑9 號催化劑處理。在一半的樣品中使用Sedgesoft ELS,且另 —半使用Mykon ffl)做爲軟化劑。兩種軟化劑均以1.5% 0WF施用。每一種樣品個別地依表Π所示之溶液塡塞,然後 在拉伸下於300°F硬化10分鐘。所有的樣品以完全相同的 方式處理,間隔被計時。 於表Π可淸楚得知(實施例Π至實施例22及控制組 ),在5次淸洗之後,Sedgesoft ELS樣品的撕裂強度相較 於Mykon HD樣品,其毫不例外地幾乎具有兩倍。除此之外 一一 90___ 本紙張尺度適用中國國家標準(CNS ) Μ規格(210X297公釐) 461927 A7 B7 五、發明説明(j 再次可見其DP値較高,顯示具有更佳平滑性 (請先閱讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 -30- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 461927 Α7 Β7 五、發明説明( Λ 經濟部智慧財產局員工消費合作社印製 o o «Ν o se缫 cn CO CN CN CN cn cn i—H V 1 ( /—N CO 〇0 £ IT) VO CN ON CO cn cn 00 £藥 #1 HJ Γτ 〇 X 〇 X o X »-H X o X 〇 X 〇 X o XJ X ϊα 琚 Ρ-^ χ \D CS cs OS 沄 CO 00 w-ϊ i〇 cs 躍味 >—H o cs »-«H »—H o o 寸 1 1 芝 沄 o l〇 Ό CN cs 沄 o CO m cs C<l cn cn p___H V 1 1 00 o〇 w-> cs 00 cn oo oo vr> μΨ, 〇 X 〇 X 〇 X X 1—^ X o X O X o X 1—t X ¥1 琚[in 爷衫X 00 vn yn o s cs 00 1〇 o 糴-> 1—Η o o CN ί—H r«H o o CN 1 1 in 〇s qi in w-i cs υ-> Os X 寸 cn v〇 寸 CN VO VD cs VO CN X os cn Mu. X X X oo X X X X —cs X 酿X —Θ 寸 ON m i〇 oo ON 〇〇 <N CO t—H G\ CS c〇 § v〇 Ό cn 〇o 120. 133. 卜 ν〇 m 網& ο 念 X cn X 〇 〇\ cs X 00 ON v〇 x CN v〇 X CM 卜 X m P: X o … X o Q\ 〇\ X X100.6 酿X cn 卜 o 00 〇 cs c^> 卜 CO ^ &: wn m 沄 s cn VO 卜 On cn 寸 1—( t>* 安w 囤雔Φ o O o o o o 〇 o 1 1 翠μ t®Sl〇fc O m 1 1 %OWF 量 i—l »Λ *~H w-i i—1 m r~H t-H t—1 v〇 »—4 ΙΟ «-H 1 1 00 W XA 00 PJ § g § g Q 1 1 擊, r-^ o 〇 CN o o ί—H ! 1 1 » o o ιτί o o o o o 〇 SS u-> w-> in m W-i to 1 1 1 1 ng m m 繼駿 ft JML t4rll St M. ft jfajL W M. W M. W _ ft M> 4JJ ft m M. -UJ ft m iSW 乐 夺 分张 廿製 辑 »~H <N CO 寸 VO r- 00 as οThis paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) 4 6 1 9 2 7 Α7 Β7 V. Description of invention (VI) (Please read the precautions on the back before filling this page) Using the same textile, taking another sample and plugging with a similar solution, the only difference is that the accelerator used as a catalyst is 2.0% OWF, and Mykon HD is used to replace Sedgesoft ELS elastomer softener. Otherwise the sample is processed in exactly the same way. Example 9 A sample of the same textile was rinsed and dehydrated in a domestic washing machine, but was not processed using any crosslinking method. Example 10 Another sample of the same textile was used as an untreated, unwashed control group. It is clear from Table I that the samples treated with the elastomer softener can obtain a higher degree of pressing durability than any sample treated with Mykon HD. For each treatment, the tensile strength and shrinkage were similar. Printed in another experiment by the Consumers ’Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs, the results are shown in Table Π. Samples of 100% cotton Oxford shirts were choked with two concentrations of formaldehyde 3.0 and 5.0% 0WF. The catalyst was treated with three concentrations of accelerator No. 9 at 0.8, 1.0 and 2.0%. Sedgesoft ELS was used in half of the samples and Mykon ffl) was used as the softener in the other half. Both softeners were applied at 1.5% 0WF. Each sample was individually plugged with the solution shown in Table II and then hardened at 300 ° F for 10 minutes under tension. All samples are processed in exactly the same way and the intervals are timed. As can be clearly seen in Table Π (Example Π to Example 22 and control group), after 5 times of rinsing, the tear strength of the Sedgesoft ELS sample compared to the Mykon HD sample, which has almost two Times. In addition, one-to-one 90___ This paper size applies the Chinese National Standard (CNS) M specification (210X297 mm) 461927 A7 B7 V. Description of the invention (j It can be seen again that its DP 値 is higher and the display has better smoothness (please first Read the notes on the reverse side and fill out this page) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economics -30- This paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 461927 Α7 Β7 V. Description of the invention (Λ Economy Printed by the Consumer Cooperative of the Ministry of Intellectual Property Bureau oo «Ν o se 缫 cn CO CN CN CN cn cn i—HV 1 (/ —N CO 〇0 £ IT) VO CN ON CO cn cn 00 £ 药 # 1 HJ Γτ 〇 X 〇X o X »-HX o X 〇X 〇X o XJ X ϊα 琚 Ρ- ^ χ \ D CS cs OS 沄 CO 00 w-ϊ i〇cs 味 味 > —H o cs»-«H» --H oo inch 1 1 Zhi 沄 ol〇Ό CN cs 沄 o CO m cs C < l cn cn p___H V 1 1 00 o〇w- > cs 00 cn oo oo vr > μΨ, 〇X 〇X 〇XX 1 — ^ X o XOX o X 1—t X ¥ 1 琚 [in Yeats X 00 vn yn os cs 00 1〇o 籴-> 1—Η oo CN ί—H r «H oo CN 1 1 in 〇s qi in wi cs υ- > Os X inch cn v〇 inch CN VO VD cs VO CN X os cn Mu. XXX oo XXXX —cs X X —Θ inch ON mi〇oo ON 〇〇 < N CO t-HG \ CS c〇§ v〇Ό cn 〇o 120. 133. bu ν〇m network & ο read X cn X 〇〇 \ cs X 00 ON v〇x CN v〇X CM X m P: X o… X o Q \ 〇 \ X X100.6 Bake X cn bu o 00 〇cs c ^ > bu CO ^ &: wn m 沄 s cn VO On cn inch 1— (t > * Ann w 雔 o o O oooo 〇o 1 1 μ t®Sl〇fc O m 1 1% OWF amount i—l »Λ * ~ H wi i—1 mr ~ H tH t—1 v〇» — 4 ΙΟ «-H 1 1 00 W XA 00 PJ § g § g Q 1 1 hit, r- ^ o 〇CN oo ί—H! 1 1» oo ιτί ooooo 〇SS u- > w- > in m Wi to 1 1 1 1 ng mm Jijun ft JML t4rll St M. ft jfajL W M. W M. W _ ft M > 4JJ ft m M. -UJ ft m iSW ; N CO inch VO r- 00 as ο

赛騷猛缫躬一>^BMW,I (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 ) Α4規格(2ί〇Χ297公釐) 46 1 927 A7 A7 B7 經濟部智慧財產局員工消費合作社印製Sai Sao fiercely bowed> ^ BMW, I (Please read the precautions on the back before filling this page) This paper size is applicable to Chinese National Standard (CNS) Α4 size (2ί〇 × 297 mm) 46 1 927 A7 A7 B7 Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs

(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) 46 192 五 發明説说( 經濟部智慧財產局員工消費合作社印製 韆 Η m A7 B7 撕裂強度2 5次洗滌 W X F 一 卜 卜 cn X 00 ON <Ν σ\ 〇\ ι—Η X 卜 r-H 寸 〇\ w-i X 卜 CO 抗張強度2 5次洗滌 W X F Ο CM X cn ON 寸 Ο 寸 X cn fS 70.1 X109.7 DP,5 次洗 滌 3.00 «-Η CO o r—^ V 匕繼 乂 ts 八 ^ CO CO X o o o 1-H X oo o o X o 耀1〇择 o <N 〇 f**4 CO cn t-π m -怒 o l〇 C4 o o CO 〇 V /«—S S3 44J LL 00 m p-H X cs as C5 X 卜 vo X 卜 vo r—H 〇〇 〇 r—4 CN o cs 撕裂強度1 盘司 W X F 〇0 r-H CO X o o r-H CM X v〇 <N 77.4 X103.8 抗張強度1 磅 W X F o so 对 X o 寸 寸 in ra m X cs CO CO 74.1 X106.7 ΪΕΦ 300/ 10 300/10 1 1 軟化 劑量 %OWF l〇 «—H vn H 1 1 軟化 劑種 類 g g 1 1 ϋΐ 〇 o cs 1 1 ch2o %OWF o o m 1 1 -娜你》訟实 握ng寐癍并鹺佟 100% 棉 100% 棉 100% 棉 辑 cs 親樂葙 (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率(CNS ) Μ規格(2!0X297公釐) 461927 五詹妈“” 度量四種18 X 36吋之螺縈Challis紡織品樣品, 使用一種處理溶液塡塞且通經擠麽滾筒以得到如表I所示 的處理化學品的數量。經處理的紡織品置於固定框(Pin frame)且在所示溫度的烤箱下硬化。經固定之紡織品由烤 箱中移出再由固定框中取出。經處理紡織品的物理性質被 測量且記錄,並示於表ΙΠ。 由表瓜可淸楚得知,基於紡織品重量(OWF)之甲醛 數量增加時可改良DP値,但是降低紡織品的強度。此結 果亦同樣地出現在縮水性數量,由結果顯示完全非預期的 DP和縮水性降低的組合。 實施例24 樣品的製備如同於實施例23中者,但係由螺縈亞麻 紡織品與必需的化學品數量來提供示於表IV之OWF値。固 化溫度爲300度但停留時間不同。結果示於表IV。 實施例25 Lenzing Lyocell螺縈紡織品依據實施例1的方法處 理以得到如表V所示的0WF化學品數量。表V顯示該方法 對Lyocell螺縈的效率。 經濟部智慧財產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)(Please read the precautions on the back before filling this page) This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) 46 192 Five inventions (printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs mΗm) A7 B7 Tear strength 2 5 washes WXF 1 卜 cn X 00 ON < N σ \ 〇 \ ι—Η X rrH inch 〇 \ wi X CO Tensile strength 2 5 washes WXF 〇 CM X cn ON Inch 〇 Inch X cn fS 70.1 X109.7 DP, 5 times washing 3.00 «-Η CO or— ^ V Dagger following 乂 ts ^ CO CO X ooo 1-HX oo oo X o Yao 1〇 select o < N 〇 f ** 4 CO cn t-π m -nuol〇C4 oo CO 〇V / «— S S3 44J LL 00 m pH X cs as C5 X Bu vo X Bu vo r—H 〇〇〇r—4 CN o cs Tear strength 1 Pan Division WXF 〇0 rH CO X oo rH CM X v〇 &N; 77.4 X103.8 Tensile strength 1 lb WXF o so to X o inch in ra m X cs CO CO 74.1 X106.7 ΪΕΦ 300/10 300/10 1 1 Softening dose% OWF l〇 «—H vn H 1 1 Type of softener gg 1 1 ϋΐ 〇o cs 1 1 ch2o% OWF oom 1 1-Na you, ng鹾 佟 10 0% cotton 100% cotton 100% cotton series cs Qinle 葙 (Please read the notes on the back before filling this page) This paper size is applicable to China National Standards (CNS) Μ specifications (2! 0X297 mm) 461927 Wu Zhan Ma "" measures four 18 x 36 inch snail Challis textile samples, using a treatment solution to plug and pass through a squeeze roller to get the amount of processing chemicals shown in Table I. The treated textile is placed in a fixed position Pin frame and hardened in the oven at the temperature shown. The fixed textiles were removed from the oven and taken out of the fixed frame. The physical properties of the treated textiles were measured and recorded and shown in Table II. It is clear that DP 値 can be improved when the amount of formaldehyde based on the weight of the textile (OWF) is increased, but the strength of the textile is reduced. This result also appears in the amount of shrinkage, and the results show completely unexpected DP and shrinkage Reduced combination. Example 24 The sample was prepared as in Example 23, but the OWF (R) shown in Table IV was provided from scotch linen textiles and the amount of necessary chemicals. The curing temperature was 300 ° C but the residence time was different. The results are shown in Table IV. Example 25 Lenzing Lyocell snail fabric was processed according to the method of Example 1 to obtain the amount of OFF chemicals as shown in Table V. Table V shows the efficiency of this method for Lyocell snails. Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs (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(2丨〇乂297公瘦) 經濟部智慧財產局員工消費合作社印製 46 1 927 A7 B7 五、發明説明(Vi ) 目撇 DP,5 次洗 滌 w-> OJ cn 13.50 | |4.00 1 o i—H VO ^ 耀躬 2.83 X +0.25 1,25 X +0.67 0.50 X +0.16 18.25 X 8,42 i撕裂或破裂強 1度揖耗% L_ 108.4 X 107,2 84.0 X 87.4 72.7 X 59.1 On X 寸· m S mm 运缌 81.5 X 75.3 74.3 X 69.2 67.8 X 50.5 86.7 X 77.2 囤酲a 300/10 300/10 300/10 1 t 尿素 %0WF o <N o CN o cs 1 1 |SM2112 '%0WF — »—H m r-H 1 1 LF催化 劑,%0WF 寸 ΓΟ CO 寸 1 1 ch2o %0WF o o o 20.0 控制組 ng oo 卜 〇\ 卜 〇 oo Γ-·This paper size applies the Chinese National Standard (Cns) A4 specification (2 丨 〇297297 thin) Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 46 1 927 A7 B7 V. Description of the Invention (Vi) DP, 5 washings w- > OJ cn 13.50 | | 4.00 1 oi—H VO ^ Flare 2.83 X +0.25 1,25 X +0.67 0.50 X +0.16 18.25 X 8,42 iTear or rupture strength 1 degree Consumption% L_ 108.4 X 107,2 84.0 X 87.4 72.7 X 59.1 On X inch m S mm Transport 81.5 X 75.3 74.3 X 69.2 67.8 X 50.5 86.7 X 77.2 Store a 300/10 300/10 300/10 1 t Urea% 0WF o < N o CN o cs 1 1 | SM2112 '% 0WF — »—H m rH 1 1 LF catalyst,% 0WF inch ΓΟ CO inch 1 1 ch2o% 0WF ooo 20.0 Control group ng oo 卜 〇 \ 卜 〇oo Γ- ·

Alm DP,1 次洗 滌 |3.50 1 CS CO |3.00 1 β & y—t ^ 0.17 X +0.91 0.42 X +0.75 0.83 X +0.50 2.00 X 0.33 Η x 锻耷 摄ΙΕ1 128.2 X 95.5 119.9 X 100.9 138.4 X 119.0 183.5 X 146.1 抗張強度 (磅),W X F 107.0 X 71.0 111.7 X 70.0 117.5 X 77.2 124.5 X 83.8 IHL; K A O W o o T—< 〇 oi 1尿素 %0WF o 1—H O f—1 〇 r-H o r 1 SM2112 %0WF W-l U-J H wn r-H LF催化 劑 %0WF cn ·< cn cn cn ch2o %0WF o in f! < 〇 o o »—h ng 奪黯 On v〇 On o ON VO ON cs VO σ\ Λ«Alm DP, 1 wash | 3.50 1 CS CO | 3.00 1 β & y-t ^ 0.17 X +0.91 0.42 X +0.75 0.83 X +0.50 2.00 X 0.33 Η x forging photo Ι1 128.2 X 95.5 119.9 X 100.9 138.4 X 119.0 183.5 X 146.1 Tensile strength (lbs), WXF 107.0 X 71.0 111.7 X 70.0 117.5 X 77.2 124.5 X 83.8 IHL; KAOW oo T— < 〇oi 1 urea% 0WF o 1-HO f-1 〇rH or 1 SM2112 % 0WF Wl UJ H wn rH LF catalyst% 0WF cn · < cn cn cn ch2o% 0WF o in f! ≪ 〇oo »—h ng Delight On v〇On o ON VO ON cs VO σ \ Λ«

DP,5 次洗 滌 MJ 3.50 4.00 |i.oo | 0.17 X +0.65 0.25 X 0.50 0.17 X 0.50 4.00 X 1.25 DP,1 次洗 滌 〇 寸· 〇 〇 4 〇 i—l Μ ^ 糴耜 |〇·42 X +0.17 0.00 X +0.17 0.17 X +0.17 2,92 X 2.00 U X 莓阳 105.0 X 67.1 68.2 X 51.5 86.22X 54.9 60.5 X 37.7 抗張強度 (磅),W X F 187.0 X 49.7 76.8 X 34.7 74.6 X 42,0 120.8X 80.8 tit $ 1 280/10 300/10 1300/10 | 1 1 尿素 %OWF ο i—l 〇 〇 1—Η 1 1 SM2112 %OWF Ό 1 < in T—i 1 1 LF催化 劑 |%OWF CO cn 对· cn 1 1 ch2o %OWF |15.0 I 〇 丨15.0 I 1 1 ng mm 〇\ ζ- 948C (請先聞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) A7 經濟部智慧財產局員工消費合作社印製 461927 B7 五、發明説明(以) DP, 5次 洗滌 3.50 |<1.〇〇| 3.50 ο CS cn ο I '«Η 3.00 ki.ool 5.00 |<l_〇〇 1 ο 寸· cn 0 1 1 i '5.00 1__ 0 1 1 '< <Ν 〇 <Ν CN Γ—^ 00 «-Η en V) Ο 卜 ΙΟ X 寸· 〇\ cs 寸 m OO CO VO ο r—H oo X X X X X X X X X X X X X X CO VO (N ο <Ν 〇 CO CN oo ν〇 oo CSJ oo <N 〇\ 〇\ o ο CS <N 〇\ fH o CO CO 寸 oi a\ 1 1 < <Ν O t*H On T*~H oo >-H DP, :1次 |洗滌 4.00 〇 ^«4 V〇 cn 3.50 Ο vn cs cn <1.00 5.00 o > "Ή \Τ) CS 5.00 o o 1—H 1—1 X 卜 ψ—t 〇 CM CO X oo m 〇 cn Os Γ-» o cs CO οο οο Vj 卜 cs CN 〇 vr> 〇 ON cn οο CO OO \〇 o X X X X X X X X X X X X X cs On On τ*~< o o ο 00 vr» CN l〇 T—H 寸 r- ο cn CO r«—( l>* cs 耀锯 ,·|__Η 〇\ rr-t t-H 寸 r—Η 〇\ 寸 CN r—( 卜 T|- OO OO cs o t-H οο CM CN CO 寸 寸 Γ-> 卜 CN Μ χ 寸· 寸 〇 r>H ι._·Η 寸 »—H yH as vn OO w-> vd Ο CS CN oo x OO i〇 vd X X X X X X X X X X X X X cn cs oo w-i CM oo 00 04 cs 寸 r-H o S 卜 IT) σ\ CS cn 00 »〇 00 § cs cn ON οο V£> o £ Ο o W-) oo 卜 m vn 卜 卜 cn 卜 cn OO s$s ^ CN <S On cn CS 沄 cs CN CO CM CN cs OJ IT) CN CN <n 寸 缌窆 X X X X X X X X X X X X X X r- o CO CO 卜 CO CM o O oo l〇 CN o o 寸· 对 «-Η 寸 CN 00 VO v〇 v〇 ON CO cs 卜 cn o <N 〇 硬化/ 時間 (T/分) 300/10 1 1 300/10 1 1 300/10 垂 1 300/10 1 1 300/10 1 1 300/10 1 t 300/10 1 幽 ο 〇 o 〇 〇 〇 o r—Η 1 1 1—H 1 1 r*H 1 1 1 1 r-H 1 1 1 1 r-H 1 1 CS —tin S 〇 m wo xn l〇 m to I »—H 1 ·—H 1 1 1 »—< I 1 ΓΤ _: 〇 CO cn cn cn cn cn CO d歡沴 1 1 寸· 1 1 1 ( 1 1 寸 1 1 1 1 1 < ch2o %0WF ο in 1 1 〇 >—H 1 1 o u-i 1 1 〇 m t-H 1 1 o r-H 1 1 〇 m o W-1 o U-i 1 1 邀 班 珐 s_ 魅 «3 Φ y ¢1 €) 蟀 蝾 BjJi Βη* «拒 ng < 逋 < 瘦 C 键 s <c 璉 c酿 < 趄 鐵 m M 0¾拒 m M m =¾识 M 女瘅 m 挺 Pi # m αί ού m Pi毖 勘 OS# 勘 pd ¢1 Dg mty iM·? IS m 00 ΟΊ 卜 |728C I σν cs I729C 1 ο CO 730C 1—H cn 731C OJ cn I732C 1 cn CO 733C ! 寸 cn 734C | (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) 46 1 927 經濟部智慧財產局員工消費合作社印製 A7 ___^_____B7___ 一種螺縈和乙酸酯紡織品依據實施例23的方法處理 以得到如表VI所示的0WF化學品數量。表V!顯示該方法對 螺縈和乙酸酯紡織品的效率。 實施例27 一種50/50螺縈/聚酯紡織品依據實施例23的方法 處理以得到如表W所示的OWF化學品數量。表W顯示該方 法對螺縈/聚酯紡織品的效率。 這個實施例顯示50/50聚酯/螺縈紡織品的效應, 其在以前並無法出售做爲可淸洗紡織品。這些紡織品並不 是一種螺縈和聚酯纖維的緊密混紡物,而是以一些區域爲 100%聚酯且其他100%螺縈的機織品。螺縈在水洗時會 縮水,聚酯則不會。這兩個纖維的不同縮水性造成紡織品 極多的波紋,使其類相似鬆餅。這種紡織品一般做爲『乾 洗』紡織品出售,但是在依據本發明方法處理後變成一種 可水洗的新產品。 實施例28 一種螺縈和亞麻(85/15)紡織品依據實施例23的 方法處理以得到如表VDI所示的OWF化學品數量。表观顯示 該方法對含螺縈紡織品的不同具體實施例。 在表中的結果顯示僅使用甲醛和催化劑的方法可達 到之結果超越業界之強度標準並且產生3.5之DP値,其 可被業者所接受。 於表中的結果顯示,含螺縈之紡織品僅使用甲醛和 (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(21〇Χ297公釐) 經濟部智慧財產局員工消費合作社印製 461927 A7 B7_________ 五、到—種紡織品係超越業界之強度標準並且 產生3.5之DP値。該紡織品可被業者所接受。 該表亦顯示’當聚矽氧烷彈性體被加至甲醛和催化 劑時,其具有非常高的強度和得到4.00之DP値。 單獨加入尿素至甲醛和催化劑中可得到比加入聚矽 氧烷更高的抗張強度’但是較低的撕裂強度’此係因爲尿 素預料會使紡織品在某程度上較硬。然而,結果仍是比單 獨使用甲醛和催化劑更佳。DP並不受到尿素的加入而改 良。 在一個較佳具體實施例中,甲醛,催化劑’聚矽氧 烷SM2112和尿素係以混合物使用,所得到的總結最佳結 果爲抗張強度和撕裂強度均顯示聚矽氧烷和尿素可能具有 協同效應。在存有聚矽氧烷時DP再次昇高至4.00。 在所有的樣品中縮水性顯著地保持不變,相較於未 經處理控制組的6.42%縮水性’其顯示大約相同大小的 延伸性。 本紙張尺度適用中國國家標準(CNS ) A4规格(210X297公釐) (請先聞讀背面之注意事項再填寫本頁)DP, 5 washings MJ 3.50 4.00 | i.oo | 0.17 X +0.65 0.25 X 0.50 0.17 X 0.50 4.00 X 1.25 DP, 1 washing 〇 inch · 〇〇4 〇i—1 Μ ^ 籴 耜 | 〇 · 42 X +0.17 0.00 X +0.17 0.17 X +0.17 2,92 X 2.00 UX Raspberry 105.0 X 67.1 68.2 X 51.5 86.22X 54.9 60.5 X 37.7 Tensile strength in pounds, WXF 187.0 X 49.7 76.8 X 34.7 74.6 X 42,0 120.8 X 80.8 tit $ 1 280/10 300/10 1300/10 | 1 1 urea% OWF ο i—l 〇〇1—Η 1 1 SM2112% OWF Ό 1 < in T—i 1 1 LF catalyst |% OWF CO cn pair · cn 1 1 ch2o% OWF | 15.0 I 〇 丨 15.0 I 1 1 ng mm 〇 \ ζ- 948C (Please read the precautions on the back before filling this page) This paper size applies Chinese National Standard (CNS) A4 Specifications (210X297 mm) A7 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 461927 B7 V. Description of the invention (with) DP, 5 washes 3.50 | < 1.〇〇 | 3.50 ο CS cn ο I '«Η 3.00 ki.ool 5.00 | < l_〇〇1 ο inch · cn 0 1 1 i '5.00 1__ 0 1 1' < < Ν 〇 < Ν CN Γ— ^ 00 «-Η en V) Ο ΒΙΟ X inch · 〇 \ cs inch m OO CO VO ο r—H oo XXXXXXXXXXXXXX CO VO (N ο < Ν 〇CO CN oo ν〇oo CSJ oo < N 〇 \ 〇 \ o ο CS < N 〇 \ fH o CO CO inch oi a \ 1 1 < < N O t * H On T * ~ H oo > -H DP,: 1 time | wash 4.00 〇 ^ «4 V〇cn 3.50 Ο vn cs cn < 1.00 5.00 o > " Ή \ Τ ) CS 5.00 oo 1—H 1—1 X Bu ψ—t 〇CM CO X oo m 〇cn Os Γ- »o cs CO οο οο Vj Bucs CN 〇vr > 〇ON cn οο CO OO \ 〇o XXXXXXXXXXXXX cs On On τ * ~ < oo ο 00 vr »CN l〇T—H inch r- ο cn CO r« — (l > * cs Yao saw, · | __Η 〇 \ rr-t tH inch r—Η 〇 \ Inch CN r— (Bu T |-OO OO cs o tH οο CM CN CO Inch Γ- > Bu CN Μ χ Inch · Inch 〇r > H ι._ · Η Inch »—H yH as vn OO w- > vd Ο CS CN oo x OO i〇vd XXXXXXXXXXXXX cn cs oo wi CM oo 00 04 cs inch rH o S (IT) σ \ CS cn 00 »〇00 § cs cn ON οο V £ > o £ Ο o W -) oo bu m vn 卜卜 cn 卜 cn OO s $ s ^ CN < S On cn CS 沄 cs CN CO CM CN cs O J IT) CN CN < n Inch 缌 窆 XXXXXXXXXXXXXX r- o CO CO COCO CM o O oo l〇CN oo Inch · For «-Η Inch CN 00 VO v〇v〇ON CO cs bucn o < N 〇Hardening / time (T / min) 300/10 1 1 300/10 1 1 300/10 vertical 1 300/10 1 1 300/10 1 1 300/10 1 t 300/10 1 quiet ο 〇o 〇〇〇 or—Η 1 1 1—H 1 1 r * H 1 1 1 1 rH 1 1 1 1 rH 1 1 CS —tin S 〇m wo xn l〇m to I »—H 1 · —H 1 1 1» — < I 1 ΓΤ _: 〇CO cn cn cn cn cn CO d 沴 1 1 inch · 1 1 1 (1 1 inch 1 1 1 1 1 < ch2o% 0WF ο in 1 1 〇 > —H 1 1 o ui 1 1 〇m tH 1 1 o rH 1 1 〇mo W-1 o Ui 1 1 Invite class s_ charm «3 Φ y ¢ 1 €) 蟀 蝾 BjJi Βη *« Reject ng < 逋 < Thin C Key s < c 琏 c 酿 < 趄 铁 m M 0 0 拒 m M m = ¾ 识 M 瘅 m Pi # m αί ού m Pi 毖 毖 OS # ppd ¢ 1 Dg mty iM ·? IS m 00 ΟΊ 卜 | 728C I σν cs I729C 1 ο CO 730C 1—H cn 731C OJ cn I732C 1 cn CO 733C! inch cn 734C | (Please read the notes on the back before filling in this page) This paper size applies to China National Standard (CNS) A4 (210X297mm) 46 1 927 Wisdom of the Ministry of Economic Affairs A7 printed by the Consumer Cooperative of the Property Bureau ___ ^ _____ B7___ A snail and acetate textile was processed according to the method of Example 23 to obtain the amount of 0WF chemicals as shown in Table VI. Table V! Shows the efficiency of this method for snails and acetate textiles. Example 27 A 50/50 snail / polyester textile was treated according to the method of Example 23 to obtain the amount of OWF chemicals as shown in Table W. Table W shows the efficiency of this method for scotch / polyester textiles. This example shows the effect of a 50/50 polyester / spiral textile, which has not previously been sold as a washable textile. These textiles are not an intimate blend of helical and polyester fibers, but are woven fabrics with 100% polyester in some areas and 100% helical in others. Snails will shrink when washed, polyester will not. The different shrinkage of these two fibers causes the textile to be extremely wavy, making it similar to a muffin. Such textiles are generally sold as "dry-washed" textiles, but after processing according to the method of the present invention, they become a new washable product. Example 28 A snail and linen (85/15) textile was treated according to the method of Example 23 to obtain the amount of OWF chemicals as shown in Table VDI. Apparently different embodiments of this method for snail-containing textiles are shown. The results in the table show that the method using only formaldehyde and catalyst can achieve results that exceed the industry's strength standard and produce a DP of 3.5, which is acceptable to the industry. The results in the table show that the textiles containing snails only use formaldehyde and (please read the precautions on the back before filling this page) This paper size applies to the Chinese National Standard (CNS) A4 specification (21 × 297 mm) Ministry of Economic Affairs Printed by the Intellectual Property Bureau Employee Cooperative Cooperative 461927 A7 B7_________ 5. The type of textiles that exceed the industry's strength standard and produce a DP of 3.5. The textile is acceptable to the industry. The table also shows that when a polysiloxane elastomer is added to formaldehyde and a catalyst, it has very high strength and obtains DP 値 of 4.00. The addition of urea to formaldehyde and the catalyst alone results in a higher tensile strength ' but a lower tear strength ' than the addition of polysiloxanes because urea is expected to make the textiles somewhat harder. However, the results are still better than using formaldehyde and catalyst alone. DP is not improved by the addition of urea. In a preferred embodiment, formaldehyde, catalyst 'polysiloxane SM2112 and urea are used in a mixture. The best results obtained are that both tensile strength and tear strength show that polysiloxane and urea may have Synergy. DP again rose to 4.00 in the presence of polysiloxane. The shrinkage remained significantly unchanged in all samples, showing an approximately the same size elongation compared to the 6.42% shrinkage ' of the untreated control group. This paper size applies to China National Standard (CNS) A4 (210X297 mm) (Please read the precautions on the back before filling this page)

46 192746 1927

7 7 A B 五、發明説明(η ) 經濟部智慧財產局員工消費合作社印製 o o 〇 o ο ο o l—H ro CN ι〇 IT) w-> cs CO cn CS ON cn CO CN ON 卜 X T~H X o X 1-Η X X o X; ^ Ρη X cn cn Ό cn m 00 1〇 ΟΟ cn o〇 廳m达 cn i—H ο r-H 〇 〇 ο I # o o o Ο 〇 Se缕 o; oi χη iA cn 〇0 CM ON 00 1〇 (Ν ΟΝ CN 〇s 水性, 欠洗滌, X F X cn CO o X <N o X ir> (N ο X cn 00 Ο X cn 00 〇 :X CS ON CO ^-H <—h ο ο 〇 侧- * mtx 酿 m 酿 锹 皲 皲 莓 m — m m mz^ 伥 伥 伥 伥 伥 m ο VO cn Ο 00 <N ο 〇〇 cn cn 00 CN o r- <M ftrf 锻*' W X >< X X X X 1ϊ- W"V CO 卜 o m 卜 σ\ Ο (Ν cs o o Ό CO ? Ϊ 〇 ο 2 o 〇 O ο Ο o O 囤酲。w 1 1 s 芝 o ΓΛ 尿素 %OWF 1 1 o i—l ο ι—Η Ο t—Η o r-< 〇 r-H cs r-^ U-4 cs ^ so CO ^ in > 4 tn ϊ—^ J I-H vn 00 寸 00 <n 1丨___丨4 tL. VJ ° —1 ¥承 cs cn cn 寸 κη ch2o %0WF o 00 Ο Ο ο ΓΟ o i〇 H ο ο <Ν 錄唣黯 ^J· IT) l—1 ι—Η 卜 卜 〇〇 Ο 1—4 链鏟盈&蚺壯张迄«铢裆* 盤s'®崧s縦迄«雄δ :龌酿ί _拗§犖趣Μ酿摄£spsmlg)4K你蛔磨郸頰豳鹦祺摄:龌蝌, m« DP", 1次 洗滌 m 〇 寸 CO o 寸 Ο ι—Η 縮水性, 1次洗滌, W X F +0.33 X +1.08 〇 + X 00 in o cn 二 + X 芝 Ο 卜 二 + X i—Η ο ί—Η X <Ν 寸 SO m - rrvf s Sliff X Is- 〇o 1 < X ί—H cn m 寸 X 寸 00 X o 3 ι—Η X 00 S; ο m ν〇 X CN CN 抗張強度 (磅), W X F vn 沄 X m Os CO ON X CN Os X 卜 〇0 os ΙΤ) X ο νη ΟΟ IT) 〇0 vo X 00 cn ON 尿素 %0WF 1 t 1 1 o f-H ο 1 t SM2112 %0WF 1 1 vr> r 1 1 1 ι〇 1 1 LF催 化劑 %0WF 寸 l〇 寸 寸 ν〇 1 1 ch2o %0WF o 〇〇 o 00 〇 00 Ο 00 « 1 ng mm ON V〇 On o τ·Ή ON CN 〇\ 973控 制組 (請先閱讀背面之注意事項再填寫本頁) 6ε 、1Τ 本紙張尺度適用中國國家標準(CMS ) A4規格(21〇Χ29<7公釐) A7 B7 (請先閱讀背面之注意事項再填寫本頁) 二種螺縈紡織品之測試係藉由在350°F的熱壓頭壓烫 15秒。此種壓烫對兩種紡織品產生極亮的光澤,當其係 置於黑色切剝(black butcher)亞麻布中更顯注。如同於 下表中所示者,經本發明方法處理後的壓烫並未有引人注 意的光澤。 紐 藉由壓燙之亮光螺縈紡織品傾向性 紡織品/顏色 未經處理 未經壓烫 未經處理 經壓烫 經處理 經壓烫 嫘縈斜紋織布/白 微光澤* 高光澤 微光澤 嫘縈亞麻布/黑 無光澤 高光澤 無光澤 在原有紡織品中的微光澤係由於使用明亮的螺縈纖 維。然而,壓燙的確可增加光澤,但是本發明的處理並未 顯示有增加的光澤,且看似原有的紡織品。 可淸楚得知者爲,本發明的處理或可避免壓烫產生 的閃亮’或可完全除去。閃亮對於螺縈紡織品而言,不僅 對消費者是一個嚴重的問題,在工廠加工時亦會因爲紡織 品碰觸熱金屬時產生亮點。 經濟部智慧財產局員工消費合作社印製 螺縈纖維在熱和壓力下產生分子運動,因此使纖維 變形造成平的點。如果產生足夠多的平點,纖維開始做用 如鏡子,其使得光不再由所有方向反射而使光由一個方向 反射造成明亮的『光澤』。如果足夠多時,對於黑色紡織 品可產生色調的完全改變。 本發明的方法因爲具有分子交聯能力使得分子結構 ^ ^-;-46______ 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 4 6 19 2 Α7 Β7 ι 織品壓燙時分子不能移軌 ,因此不會產生 平的點,使紡織品看似與原來未經壓燙的相同。 (請先閱讀背面之注意事項再填寫本頁) 這個性質極具有價値,因爲自從由1920年底或1930 年螺縈出現至市面開始,螺縈的壓燙光澤一直是個困擾。 一般人會推測,由本發明方法所形成的普遍交聯作用使無 光澤效應遠佳於由樹脂中所得到者,其中大部份的光滑係 因爲在大量地無定形螺縈纖維中存有樹脂所致。那是爲什 麼經淸洗的螺縈紡織品在樹脂鬆散後,在電熨斗壓燙時有 過度的光澤。 下面的實施例說明應用該方法至絲或羊毛製成的紡 織品。 實施例307 7 AB V. Description of Invention (η) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs oo 〇 ο ο ol—H ro CN ι〇IT) w- > cs CO cn CS ON cn CO CN ON bu XT ~ HX o X 1-Η XX o X; ^ Ρη X cn cn Ό cn m 00 1〇〇OO cn o〇 Hall m reaches cn i—H ο rH 〇〇ο I # ooo 〇 〇Se strand o; oi χη iA cn 〇0 CM ON 00 1〇 (Ν ΟΝ CN 〇s water-based, underwash, XFX cn CO o X < N o X ir > (N ο X cn 00 〇 X cn 00 〇: X CS ON CO ^ -H < —H ο ο 〇 side- * mtx stuffed m stuffed shovel m — mm mz ^ 伥 伥 伥 伥 伥 m ο VO cn 〇 00 < N ο 〇〇cn cn 00 CN o r- < M ftrf Forging * 'WX > < XXXX 1ϊ- W " V CO 卜 om 卜 σ \ Ο (Ν cs oo Ό CO? Ϊ 〇ο 2 o 〇O ο 〇 o O stockpile. W 1 1 s Zhi o ΓΛ urea % OWF 1 1 oi—l ο ι—Η Ο t—Η o r- < 〇rH cs r- ^ U-4 cs ^ so CO ^ in > 4 tn ϊ— ^ J IH vn 00 inch 00 < n 1 丨 ___ 丨 4 tL. VJ ° —1 ¥ 承 cs cn cn inch κη ch2o % 0WF o 00 Ο Ο ο ΓΟ oi〇H ο ο < Ν 唣 唣 ^ ^ J · IT) l—1 ι—Η 卜卜 〇〇 1-4 chain shovel surplus & strong expansion so far «baht crotch * Song disk s'® s Cong until «male [delta]: filthy stuffed ί _ § bend Luo interest Μ stuffed photo £ spsmlg) 4K roundworm you wear Dan buccal parrot Qi Bin subject: filthy tadpole, m« DP ", 1 wash m 〇inch CO o inch 〇 ι—Η Shrinkage, 1 wash, WXF +0.33 X +1.08 〇 + X 00 in o cn Ⅱ + X 芝 〇 卜 二 + X i—Η ο ί—Η X < Ν inch SO m-rrvf s Sliff X Is- 〇o 1 < X ί—H cn m inch X inch 00 X o 3 ι—Η X 00 S; ο m ν〇X CN CN tensile strength (pounds), WXF vn沄 X m Os CO ON X CN Os X Bu 0 0 os ΙΤ) X ο νη ΟΟ IT) 〇0 vo X 00 cn ON Urea% 0WF 1 t 1 1 o fH ο 1 t SM2112% 0WF 1 1 vr > r 1 1 1 ι〇1 1 LF catalyst% 0WF inch l0 inch inch ν〇1 1 ch2o% 0WF o 〇〇o 00 〇00 〇 00 «1 ng mm ON V〇On o τ · Ή ON CN 〇 \ 973 control group ( Please read the notes on the back before filling out this page) 6ε, 1T This paper size applies Chinese National Standard (CMS) A4 specification (21〇 Χ29 < 7 mm) A7 B7 (Please read the precautions on the back before filling out this page) The two types of snail textiles are tested by pressing at 350 ° F for 15 seconds. This stamping produces an extremely bright sheen to both textiles, which is even more noticeable when placed in black butcher linen. As shown in the table below, the press after the treatment of the method of the present invention did not have a noticeable gloss. Shiny snails with embossed fabrics. Favorite textiles / colors: untreated, unpressed, untreated, pressed, treated, pressed, twill weave / white microgloss * high gloss microgloss, linen Cloth / black matt high gloss matt in the original textile due to the use of bright snail fiber. However, pressing does increase gloss, but the treatment of the present invention does not show increased gloss and looks like the original textile. It can be clearly understood that the treatment of the present invention can avoid the shinyness caused by pressing or can be completely removed. Shining is not only a serious problem for consumers of snail textiles, but also causes bright spots when textiles touch hot metal during processing in factories. Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs The snail fiber generates molecular motion under heat and pressure, thus deforming the fiber to create flat spots. If there are enough flat spots, the fiber starts to function as a mirror, which makes the light no longer reflected in all directions and makes the light reflected in one direction to cause a bright "gloss". If enough, a complete change in hue can be produced for black textiles. The method of the present invention has a molecular cross-linking ability to make the molecular structure ^ ^-; -46 ______ This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) 4 6 19 2 Α7 Β7 ι molecules cannot be moved during fabric pressing Rail, so no flat spots are produced, making the textile look the same as it was before. (Please read the notes on the back before filling out this page.) This property is extremely valuable, since the snail's hot gloss has been a problem since the end of 1920 or 1930 when it appeared on the market. The average person would speculate that the general cross-linking effect formed by the method of the present invention makes the matte effect much better than that obtained from the resin. Most of the smoothness is caused by the presence of the resin in a large amount of amorphous snail fiber. . That's why the washed snail textiles have excessive gloss when the iron is pressed after the resin is loosened. The following examples illustrate the application of this method to textiles made from silk or wool. Example 30

X 度量三種18 X 36吋之羊毛Challis紡織品樣品和 一種絲紡織品樣品,使用一種處理溶液塡塞且通經擠壓滾 筒以得到如表X所示的處理化學品的數量。經處理的紡織 品置於固定框且在所示溫度的烤箱下硬化。經固定之紡織 品由烤箱中移出再由固定框中取出。經處理紡織品的物理 性質被測量且記錄,並示於表X。 經濟部智慧財產局員工.消費合作社印製 由表X可淸楚得知,基於紡織品重量(OWF)之甲醛 數量增加時可改良DP値,但是降低紡織品的強度。此結 果亦同樣地出現在縮水性數量,由結果顯示完全非預期的 DP和縮水性降低的組合。 本紙張尺度適用中國國家標準(CNS ) A4規格(21〇Χ297公釐) 461927 經濟部智慧財產局員工消費合作社印製 A7 _ B7 五、發明説明(^ ) IT) cs vr> CO cs 〇 Q α躬 CO CO cn «—H cn CsJ cn oo 卜 cn CO 卜 m CN in 卜 oi oi ΟΪ T—^ οά X #1躬^ X X X X X 00 ir> oo XTi 00 vn o V〇 寸 ^j- «—H r-H i—4 vn in CN o 寸 CO 〇 沄 Ω α躬 cn oi m oj cs ^ cn oo f-H CN 寸 Os CN o 佘 卜 cs oo 〇 X XI X X X X o oo o cn CO 卜 CN 〇\ 寸 f~H ON 卜 寸 o 寸 oo m oo (N cs 沄 vd m X x X X X X Μξ,Χ iT) q cn H 心 as 寸· cn CO v~> jX CO 卜 o i〇 <N m VsD 一 00 iTi Ό Os VO .fW/f 瞬 X X X X X: X 1® f x cn CO oo I-< 卜 cn 挺氅择 oo m oo cn o oo 〇\ cn 〇\ 1 5 o o 〇 O r*H IS题£ o o o o 沄 沄 沄 t 1 o m t 1 on ^ 〇 IT) iT) VO 00 ^ »—H «—H 1 »~·Η 1 LL, . n w vr^ 〇J o m 1 1 o 1 1 tL. gg o o o u ^ ^J- VO 1 1 \〇 1 1 ng 鹚 繼 仲展 M 轿 轿 挤 繁 繼ng龌 〇\ ITi CO On >〇 Os m 〇\ 〇\ ε; IT) 00 (請先閱讀背面之注意事項再填寫本頁) 、1T: 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐)X measures three 18 X 36 inch wool Challis textile samples and one silk textile sample, which was choked using a treatment solution and passed through a squeeze roller to obtain the amount of treatment chemicals shown in Table X. The treated textile is placed in a fixed frame and hardened in an oven at the temperature indicated. The fixed textiles are removed from the oven and removed from the fixed frame. The physical properties of the treated textiles were measured and recorded and are shown in Table X. Printed by employees of the Intellectual Property Bureau of the Ministry of Economic Affairs. Consumption cooperatives. From Table X, it can be clearly seen that DP 値 can be improved when the amount of formaldehyde based on the weight of textiles (OWF) is increased, but the strength of textiles is reduced. This result also appeared in the amount of shrinkage, and the result showed a completely unexpected combination of DP and reduced shrinkage. This paper size applies the Chinese National Standard (CNS) A4 specification (21〇 × 297 mm) 461927 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs A7 _ B7 V. Description of the invention (^) IT) cs vr > CO cs 〇Q α COCO CO cn «—H cn CsJ cn oo COcn CO mm CN in 卜 oi oi ΟΪ T— ^ οά X # 11 ^ XXXXX 00 ir > oo XTi 00 vn o V〇inch ^ j-« —H rH i—4 vn in CN o inch CO 〇 沄 Ω α bow cn oi m oj cs ^ cn oo fH CN inch Os CN o 佘 卜 cs oo 〇X XI XXXX o oo o cn CO bu CN 〇 \ inch f ~ H ON Inch o Inch oo m oo (N cs 沄 vd m X x XXXX Μξ, χ iT) q cn H heart as inch · cn CO v ~ > jX CO oioi < N m VsD 1.00 iTi Ό Os VO .fW / f Instant XXXXX: X 1® fx cn CO oo I- < bu cn 氅 choice oo m oo cn o oo 〇 \ cn 〇 \ 1 5 oo 〇O r * H IS title £ oooo 沄 沄 沄 t 1 omt 1 on ^ 〇IT) iT) VO 00 ^ »—H« —H 1 »~ · Η 1 LL,. Nw vr ^ 〇J om 1 1 o 1 1 tL. Gg ooou ^ ^ J- VO 1 1 \ 〇1 1 ng 鹚Following the Zhongzhan M car crowding ng 龌 〇 \ ITi CO On > 〇Os m 〇 \ 〇 \ ε; IT) 00 (Please read the precautions on the back before filling this page), 1T: This paper size applies China National Standard (CNS) Α4 specification (210 × 297 mm)

Claims (1)

—__4^4-9-? 7公告本_ A8 B8 C8 D8 修正 經濟部智慧財產局員工消費合作社印製 六、申請蓴利範圍 1·一種處理選自含纖維素纖維或蛋白質纖維所組成 之族群中之織物紡織品以達到或增強該紡織品—種選自改 善壓燙持久性性質、降低在整理期間紡織品強度的損失、 降低紡織品縮水性及改善水洗能力所組成之族群中之性質 的方法’該方法包括: 將該紡織品置入含甲醛之水溶液內以得到在該紡織品中有 效量溶液之濕吸收(wet PickuP) ’ . 將有效量之催化劑施加至該紡織品內用以催化甲醛和紡織 品之間的反應; 之後將該濕紡織品曝露至溫度爲300°F,使甲醛由該經曝 露紡織品中實質移除之前令甲醛與紡織品反應而達到或增 強該紡織品之性質; 其中該紡織品係爲未經樹脂化。 2·—種處理選自含纖維素纖維或蛋白質纖維所組成 之族群中之織物紡織品以增強該紡織品一種選自改善壓燙 持久性性質、降低在整理期間紡織品強度的損失、降低紡 織品縮水性及改善水洗能力所組成之族群中之性質的方法 ,該方法包括: . 在環境溫度下使用甲醛水溶液和催化劑處理該紡織品以催 化甲醛和該紡織品之間的反應; 將紡織品置入具有300°F昇高溫度之加熱區域而將在環境 溫度下處理之紡織品直接置於該昇高溫度使甲醛與紡織品 反應而增強紡織品的性質; 其中該紡織品係爲未經樹脂化。 1 . ^-----/ …i衣--------11 l· l·------線 (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(210 X 297公釐) 461927 A8 B8 C8 D8 六、申請專利範圍 3·—種使用甲醛處理選自含纖維素纖維或蛋白質纖 維所組成之族群中之織物紡織品以增強該紡織品一種選自 改善壓烫持久性性質、降低在整理期間紡織品強度的損失 、降低紡織品縮水性及改善水洗能力所組成之族群中之性 質的方法,該方法包括: 以甲醛處理含有選自包含纖維素纖維和蛋白質纖維所組成 之族群中之紡織品,而使甲醛與該纖維素或蛋白質纖維反 應,及 接枝一彈性體至該纖維素或蛋白質纖維上; 其中該紡織品係爲未經樹脂化。 4 .根據申請專利範圍第1項之方法,其爲一種連續 方法以處理織物紡織品,其包括: 將該紡織品連續地置入一水溶液內以得到在該紡織品中有 效量溶液之濕吸收,其中該溶液包含一有效量之甲醛與一 .催化劑用於催化甲醛與紡織品之間的反應; 之後將該濕紡織品連續地曝露至溫度爲300°F’使甲醛由 該經曝露紡織品中實質移除之前令甲醛與紡織品反應而達 到或增強紡織品之性質。 . 5 .根據申請專利範圍第4項之方法、,其中該織物紡 織品含有纖維素或蛋白質纖維之天然纖維。 : 6·根據申請專利範圍第4項之方法,其中該纖維爲 棉纖維。 7 .根據申請專利範圍第4項之方法,其中該纖維爲 嫘縈纖維且該處理可控制縮水性。 2 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閲讀背面之注意事項再填寫本頁) "--------訂 ------線 經濟部智慧財產局員工消費合作社印製 經濟部智慧財產局員工消費合作社印制衣 4 6 1 927 as C8 D8 六、申請專利範圍 8·根據申請專利範圍第5項之方法,其中該天然纖 維爲棉或絲纖維之蛋白質纖維。 9 ·根據申請專利範圍第1項之方法,其中含尿素或 其衍生物之水溶液施加至該紡織品。 10 ·根據申請專利範圍第5項之方法,其中足以降低 紡織品在洗滌後之強度損失之含量之彈性體在甲醛與紡織 品反應而增強紡織品性質之前施加至該紡織品。 11 ·根據申請專利範圍第10項之方法,其中該彈性 體爲一種反應性彈性體。 12 ·根據申請專利範圍第11項之方法,其中該紡織 品在處理之後保留有親水性。 13 ·根據申請專利範圍第10項之方法,其中該彈性 體爲膜生成聚矽氧烷彈性體。 14 ·根據申請專利範圍第1項之方法,其中在紡織品 中溶液之濕吸收爲紡織品之20重量%。 15 ·根據申請專利範圍第14項之方法,其中該濕吸 收爲30%。 16 ·根據申請專利範圍第15項之方法,其中該濕吸 收爲由30至60%。 17 ·根據申請專利範圍第1項之方法,其中該紡織品 曝露於300°F之溫度係藉由將該紡織品置入加熱至溫度由 300°F至350°F的加熱室內。 18 ·根據申請專利範圍第1項之方法,其中該紡織品 在施用甲醒水溶液之前以水溶液濕潤。 3 „ Γ----- ,取---------^ » l· l·------線,: (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(210 X 297公釐) 46 1 927 g8s .C8 D8 六、申請專利範圍 19 · 一種親水性之壓燙持久性紡織品,其含有之紡織 品具有甲醛交聯物和彈性體接枝物。 20 ·根據申請專利範圍第19項之紡織品,其中該接 枝物爲聚矽氧烷彈性體接枝物且該紡織品爲含有纖維素。 (請先閱讀背面之注意事項再填寫本頁) I . 線· 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) 公告本 申請曰期 案 號 類 別 d〇4 Α)—__ 4 ^ 4-9-? 7 Bulletin _ A8 B8 C8 D8 Amendment printed by the Consumers ’Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 6. Application for Profits 1. A group selected from the group consisting of cellulose fiber or protein fiber Fabrics to achieve or enhance the textiles-a method selected from the group consisting of improving the permanence properties of pressing, reducing the loss of textile strength during finishing, reducing the shrinkage of textiles, and improving the ability to wash Including: placing the textile in an aqueous solution containing formaldehyde to obtain an effective amount of wet pickuP of the solution in the textile; and applying an effective amount of a catalyst to the textile to catalyze the reaction between the formaldehyde and the textile ; Then exposing the wet textile to a temperature of 300 ° F, allowing formaldehyde to react with the textile to achieve or enhance its properties before the formaldehyde is substantially removed from the exposed textile; wherein the textile is unresinified. 2 · —treating fabric textiles selected from the group consisting of cellulose fibers or protein fibers to enhance the textiles one selected from the group consisting of improving pressing durability, reducing the loss of textile strength during finishing, reducing the shrinkage of textiles, and A method for improving properties in a group of water-washing capabilities, the method comprising: treating the textile with an aqueous formaldehyde solution and a catalyst at ambient temperature to catalyze the reaction between the formaldehyde and the textile; placing the textile at 300 ° F High temperature heating area and textiles treated at ambient temperature are directly placed at the elevated temperature to react formaldehyde with the textile to enhance the properties of the textile; wherein the textile is unresinified. 1. ^ ----- /… i clothing -------- 11 l · l · ------ line (Please read the precautions on the back before filling this page) This paper size is applicable to China National Standard (CNS) A4 Specification (210 X 297 mm) 461927 A8 B8 C8 D8 VI. Application for Patent Scope 3. · Use formaldehyde to treat fabrics and textiles selected from the group consisting of cellulose fiber or protein fiber to enhance The textile is a method selected from the group consisting of improving pressing durability properties, reducing loss of textile strength during finishing, reducing textile shrinkage, and improving water washability, the method comprising: treating with formaldehyde containing Textiles in a group consisting of cellulose fibers and protein fibers, and reacting formaldehyde with the cellulose or protein fibers, and grafting an elastomer onto the cellulose or protein fibers; wherein the textile is unresinified . 4. The method according to item 1 of the scope of patent application, which is a continuous method for treating fabric textiles, comprising: continuously placing the textile in an aqueous solution to obtain a wet absorption of an effective amount of a solution in the textile, wherein the The solution contains an effective amount of formaldehyde and a catalyst for catalyzing the reaction between formaldehyde and textiles; the wet textile is then continuously exposed to a temperature of 300 ° F 'to substantially remove formaldehyde from the exposed textiles. Formaldehyde reacts with textiles to achieve or enhance the properties of textiles. 5. The method according to item 4 of the scope of patent application, wherein the textile fabric contains natural fibers of cellulose or protein fibers. : 6. The method according to item 4 of the scope of patent application, wherein the fiber is a cotton fiber. 7. The method according to item 4 of the scope of patent application, wherein the fiber is a rayon fiber and the treatment can control the shrinkage. 2 This paper size applies to China National Standard (CNS) A4 (210 X 297 mm) (Please read the precautions on the back before filling this page) " -------- Order ------ Printed by the Consumers ’Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs Printed by the Consumers’ Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 4 6 1 927 as C8 D8 6. Application for Patent Scope 8. The method according to Item 5 of the Patent Scope, where the natural fiber It is a protein fiber of cotton or silk fiber. 9-The method according to item 1 of the scope of patent application, wherein an aqueous solution containing urea or a derivative thereof is applied to the textile. 10. The method according to item 5 of the scope of patent application, wherein the elastomer sufficient to reduce the strength loss of the textile after washing is applied to the textile before the formaldehyde reacts with the textile to enhance the textile properties. 11-The method according to item 10 of the application, wherein the elastomer is a reactive elastomer. 12-A method according to item 11 of the patent application, wherein the textile remains hydrophilic after processing. 13. The method according to item 10 of the application, wherein the elastomer is a film-forming polysiloxane elastomer. 14. The method according to item 1 of the scope of patent application, wherein the wet absorption of the solution in the textile is 20% by weight of the textile. 15 The method according to item 14 of the scope of patent application, wherein the wet absorption is 30%. 16. The method according to item 15 of the scope of patent application, wherein the wet absorption is from 30 to 60%. 17. The method according to item 1 of the scope of patent application, wherein the textile is exposed to a temperature of 300 ° F by placing the textile in a heating chamber heated to a temperature of 300 ° F to 350 ° F. 18. The method according to item 1 of the scope of patent application, wherein the textile is wet with an aqueous solution before applying the aqueous solution. 3 „Γ -----, take --------- ^» l · l · ------ line: (Please read the precautions on the back before filling this page) The paper size Applicable to China National Standard (CNS) A4 specification (210 X 297 mm) 46 1 927 g8s .C8 D8 6. Application for patent scope 19 · A kind of hydrophilic stamping and durable textiles, which contains formaldehyde cross-linked substances and Elastomer graft. 20 • The textile according to item 19 of the scope of patent application, wherein the graft is a polysiloxane elastomer graft and the textile contains cellulose. (Please read the precautions on the back before reading) (Fill in this page) I. Line · Printed by the Consumers' Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs, the paper size is applicable to the Chinese National Standard (CNS) A4 (210 X 297 mm). A4 C4 461927 集·—專利説明書 發明 一、名稱 新型 中 文 織物整理方法 英 文 TEXTILE FINISHING PROCESS 姓 名 國 籍 喬治L.佩葉 裝 發明 創作 人 住、居所 姓 名 (名稱) 美國 美國俄亥俄州45236,辛辛那提市,桂溫路7781號 訂 美國紡織解決公司 線 經濟部智慧对4./..;Η工消費合作社印製 申請人 國 籍 住、居所 (事務所) 代表人 姓 名 美國 美國俄亥俄州45212,辛辛那提市,塞克遜大道 5050 號喬治L.史垂克 1 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 46 1927 A7 B7 ^aio.23 年月日夕 經濟部智慧財產局員工消費合作社印製 五、發明說明(7) 彈性體可連同甲醛和催化劑水溶液施用至紡織品。此 係將所有的處理化學品同時施用至在一種處理溶液中的紡 織品。然而,所必需的化學品’包括水和選用的成份,可 在方法進行期間的任何時間內依續地施用至紡織品內,只 要該順序不妨礙紡織品中所需之處理水平。彈性體之取得 通常爲商用的乳化劑。可使用於本發明方法之含特定彈性 體的組成物包括在含有少量彈性體之組成物倒至開放表面 且放置乾燥時乾燥形成之薄膜具有彈性體性質者。此爲一 種簡單測試以決定彈性體是否在該方法中有用。如果所選 用的彈性體造成經處理的紡織品爲親水性則更爲有利。親 水性的紡織品,亦即並不排斥水者,通常對穿著者而言具 有更高舒適性。本發明之含親水性(遇水可濕)壓燙持久 性纖維的紡織品具有甲醛交聯物及彈性體接枝物。該紡織 品較佳具有聚矽氧烷彈性體接枝物且該包括螺縈的紡織品 /較佳爲含纖維素。 雖然可使用任何彈性體,聚矽氧烷彈性體爲特別佳者 。任何的聚矽氧烷彈性體可被使用於本發明。聚矽氧烷彈 性體爲習知的材料。聚矽氧烷彈性體爲下列通式.地具有一 主鏈係由砂和氧組成,其中有機取代基連接至矽原子且包 含η個重複單位: R1 I -Si ~〇-—— I R ' n 9 本紙張尺度適用中國國豕標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再填寫本頁) ------— r 訂·?;-------線 —__4^4-9-? 7公告本_ A8 B8 C8 D8 修正 經濟部智慧財產局員工消費合作社印製 六、申請蓴利範圍 1·一種處理選自含纖維素纖維或蛋白質纖維所組成 之族群中之織物紡織品以達到或增強該紡織品—種選自改 善壓燙持久性性質、降低在整理期間紡織品強度的損失、 降低紡織品縮水性及改善水洗能力所組成之族群中之性質 的方法’該方法包括: 將該紡織品置入含甲醛之水溶液內以得到在該紡織品中有 效量溶液之濕吸收(wet PickuP) ’ . 將有效量之催化劑施加至該紡織品內用以催化甲醛和紡織 品之間的反應; 之後將該濕紡織品曝露至溫度爲300°F,使甲醛由該經曝 露紡織品中實質移除之前令甲醛與紡織品反應而達到或增 強該紡織品之性質; 其中該紡織品係爲未經樹脂化。 2·—種處理選自含纖維素纖維或蛋白質纖維所組成 之族群中之織物紡織品以增強該紡織品一種選自改善壓燙 持久性性質、降低在整理期間紡織品強度的損失、降低紡 織品縮水性及改善水洗能力所組成之族群中之性質的方法 ,該方法包括: . 在環境溫度下使用甲醛水溶液和催化劑處理該紡織品以催 化甲醛和該紡織品之間的反應; 將紡織品置入具有300°F昇高溫度之加熱區域而將在環境 溫度下處理之紡織品直接置於該昇高溫度使甲醛與紡織品 反應而增強紡織品的性質; 其中該紡織品係爲未經樹脂化。 1 . ^-----/ …i衣--------11 l· l·------線 (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(210 X 297公釐)A4 C4 461927 Collection · —Patent Specification Invention I. Name New Chinese Fabric Finishing Method English TEXTILE FINISHING PROCESS Name Nationality George L. Peyer Packing Invention Creator Residence, Residence Name (Name) United States Ohio 45236, Cincinnati, Guizhou Wenlu Road No. 7781 was ordered by the US Department of Textiles Solution Company ’s Department of Economic Wisdom 4 ./ ..; Machining Consumer Cooperative Co., Ltd. printed the applicant ’s nationality, residence (office). George L. Stryker 5050 Xun Avenue 1 This paper size is in accordance with the Chinese National Standard (CNS) A4 (210X297 mm) 46 1927 A7 B7 2. Description of the invention (7) Elastomer can be applied to textiles together with formaldehyde and aqueous catalyst solution. This is the simultaneous application of all treatment chemicals to the textile in one treatment solution. However, the necessary chemicals', including water and selected ingredients, can be applied to the textile one after the other at any time during the method as long as the sequence does not interfere with the level of processing required in the textile. The acquisition of elastomers is usually a commercial emulsifier. The specific elastomer-containing composition which can be used in the method of the present invention includes those having a elastomeric property when the composition containing a small amount of elastomer is poured onto an open surface and the film formed by drying when left to dry. This is a simple test to determine if an elastomer is useful in this method. It is even more advantageous if the elastomer chosen makes the treated textile hydrophilic. Water-repellent textiles, that is, those that do not repel water, are generally more comfortable for the wearer. The textile containing hydrophilic (wetted with water) embossed permanent fibers has formaldehyde cross-linkers and elastomer grafts. The textile preferably has a polysiloxane elastomer graft and the textile including snails / preferably contains cellulose. Although any elastomer can be used, polysiloxane elastomers are particularly preferred. Any polysiloxane elastomer can be used in the present invention. Polysiloxane elastomers are known materials. The polysiloxane elastomer has the following general formula. The ground has a main chain system composed of sand and oxygen, in which an organic substituent is connected to a silicon atom and contains n repeating units: R1 I -Si ~ 〇 -—— IR 'n 9 This paper size applies to China National Standard (CNS) A4 (210 X 297 mm) (Please read the precautions on the back before filling out this page) -------- r Order ·?; ---- --- Line —__ 4 ^ 4-9-? 7 Bulletin _ A8 B8 C8 D8 Amendment printed by the Consumers' Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 6. Application for profit scope 1. A treatment selected from cellulose-containing fiber or protein fiber A group of woven textiles to achieve or enhance the textile—a property selected from the group consisting of improved pressing durability properties, reduced loss of textile strength during finishing, reduced textile shrinkage, and improved water washability Method 'The method includes: placing the textile in an aqueous solution containing formaldehyde to obtain an effective amount of wet pickuP of the solution in the textile'. Applying an effective amount of a catalyst to the textile to catalyze formaldehyde and textile The reaction between the textiles is then exposed to a temperature of 300 ° F, and the formaldehyde reacts with the textiles to achieve or enhance the properties of the textiles before the formaldehyde is substantially removed from the exposed textiles; wherein the textiles are Not resinized. 2 · —treating fabric textiles selected from the group consisting of cellulose fibers or protein fibers to enhance the textiles one selected from the group consisting of improving pressing durability, reducing the loss of textile strength during finishing, reducing the shrinkage of textiles, and A method for improving properties in a group of water-washing capabilities, the method comprising: treating the textile with an aqueous formaldehyde solution and a catalyst at ambient temperature to catalyze the reaction between the formaldehyde and the textile; placing the textile at 300 ° F High temperature heating area and textiles treated at ambient temperature are directly placed at the elevated temperature to react formaldehyde with the textile to enhance the properties of the textile; wherein the textile is unresinified. 1. ^ ----- /… i clothing -------- 11 l · l · ------ line (Please read the precautions on the back before filling this page) This paper size is applicable to China National Standard (CNS) A4 specification (210 X 297 mm)
TW88104401A 1998-09-30 1999-03-20 Textile finishing process TW461927B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/163,319 US6511928B2 (en) 1998-09-30 1998-09-30 Rayon fabric with substantial shrink-resistant properties
US09/267,654 US6375685B2 (en) 1997-05-13 1999-03-15 Textile finishing process

Publications (1)

Publication Number Publication Date
TW461927B true TW461927B (en) 2001-11-01

Family

ID=26859536

Family Applications (1)

Application Number Title Priority Date Filing Date
TW88104401A TW461927B (en) 1998-09-30 1999-03-20 Textile finishing process

Country Status (3)

Country Link
MA (1) MA24783A1 (en)
PE (1) PE20000587A1 (en)
TW (1) TW461927B (en)

Also Published As

Publication number Publication date
PE20000587A1 (en) 2000-08-09
MA24783A1 (en) 1999-10-01

Similar Documents

Publication Publication Date Title
CA1085563A (en) Textile treating compositions
JP2831409B2 (en) Starch containing curable amine-functional silicone for fabric wrinkle reduction and shape retention
US6375685B2 (en) Textile finishing process
US6565612B2 (en) Shrink resistant rayon fabrics
US2839429A (en) Treatment of cellulosic textile materials
US6511928B2 (en) Rayon fabric with substantial shrink-resistant properties
Montazer et al. Application of polyurethane/citric acid/silicone softener composite on cotton/polyester knitted fabric producing durable soft and smooth surface
TWI299068B (en)
TW461927B (en) Textile finishing process
JPS6071771A (en) Silicone permanent press fiber treating method and obtained product
EP1100990B1 (en) Durable press/wrinkle-free process
Xin et al. Easy-care treatments for fabrics and garments
US20010049247A1 (en) Methods for reducing fabric drying time and fabrics with improved properties
WO2001096653A1 (en) Anionically derivatised cotton for improved comfort and care-free laundering
Talebpour et al. Effects of silicone-based softener on the easy-care finished cotton fabric
Ghosh et al. Modification of jute by some low molecular weight glycols and a polyol under thermal treatment
EP1297215A1 (en) Process for applying softeners to fabrics
GB2360795A (en) Anionically dyeable, durable press, natural fibre products
Mondal et al. Surface Modification of Viscose Fabric with Silane Coupling Agents‐An Aspect of Comfort Properties
US6953485B2 (en) Enhanced fabric comprising substrates and process to provide same
Thaseen Durable press treatments to cotton, viscose, bamboo and tencel fabrics
Xin et al. The Hong Kong Polytechnic University, Kowloon, Hong Kong
JPH02182976A (en) Textile treating agent