TWI225508B - Yellow reactive dye composition - Google Patents

Yellow reactive dye composition Download PDF

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TWI225508B
TWI225508B TW88115229A TW88115229A TWI225508B TW I225508 B TWI225508 B TW I225508B TW 88115229 A TW88115229 A TW 88115229A TW 88115229 A TW88115229 A TW 88115229A TW I225508 B TWI225508 B TW I225508B
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Taiwan
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dyeing
dye
formula
dye composition
test
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TW88115229A
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Chinese (zh)
Inventor
Bau-Kuen Lai
Rung-Fang Ye
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Everlight Chem Ind Corp
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Abstract

A yellow reactive dye composition, which includes two different yellow reactive dyes, is disclosed. The yellow reactive dye composition disclosed here is a reactive dye composition with good stability, build-up, light fastness and wet fastness. The yellow reactive dye composition is suitable for the natural and regenerated cellulose fibers in exhaust dyeing, printing and continuous dyeing.

Description

12255081225508

五、發明說明(/ ) 【發明背景】 (請先閱讀背面之注意事項再填寫本頁) 本發明係有關一種可染印纖維物質之染料組成物,特 別是有關於一種適用於纖維素纖維(ceUul〇se fiber)或含纖 維素纖維之纖維物質的染色或印染的反應性黃色染料組成 物。 纖維素纖維物質或含纖維素之纖維物質的染色或印 染,其所需的反應性染料必須在各種性質上都有極佳的表 現,如均染性(leveling)、再現性(reproducibi出力、溶解度 (solubility)及堅牢度(fastness)等。 黃色反應性染料特別必須是在染深性、再現性、色彩 鮮盤性、均染性及洗潔性等方面有高品質。此外,它們必 須使染色或印染的產品具有優良的耐光、耐汗、耐氯漂之 染色堅牢度,以及長時間的高度安定性。 經濟部智慧財產局員工消費合作社印製 然而市售的黃色反應性染料,普遍都有深色染色時染 深力度不佳、不易達到所希望的染色深度;或是染深性佳, 但是染料色系帶有紅光;亦或是不能做拔染(discharge)和 防印染(resist printing)的染底;再或者是在冷壓捲染(c〇ld pad batch)染色時’其上色時間(batch time)太長,不適合 於短時間的捲置染著,是為其缺點。因此這些黃色反應性 染料總是不能令人滿意。 【發明之概述】 3 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公爱) 1225508V. Description of the invention (/) [Background of the invention] (Please read the precautions on the back before filling out this page) The present invention relates to a dye composition capable of printing fiber materials, and particularly to a kind of cellulose fiber ( ceUulose fiber) or a reactive yellow dye composition for dyeing or printing of fibrous matter containing cellulose fibers. For the dyeing or printing of cellulosic fibrous material or cellulose-containing fibrous material, the reactive dyes required must have excellent performance in various properties, such as leveling, reproducibi output, solubility (solubility) and fastness (fastness), etc. Yellow reactive dyes must have high quality, especially in terms of deepness, reproducibility, color freshness, leveling, and detergency. In addition, they must make dyeing Or dyed products have excellent light fastness, sweat resistance, chlorine bleaching resistance, and high stability for a long time. Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs, however, commercially available yellow reactive dyes are generally available. When dyeing dark colors, the dyeing strength is not good and it is difficult to reach the desired dyeing depth; or the dyeing is good, but the dye color has red light; or it cannot be discharged and resist printing ); Or in cold pad batch dyeing, its' batch time is too long, and it is not suitable for short-term roll dyeing. Point. Therefore the yellow reactive dye is not always satisfactory. [3] Summary of the Invention The sheet scale applies China National Standard (CNS) A4 size (210 X 297 Kimiyoshi) 1225508

五、發明說明(上) 為得到染料安定性和染深性佳,且工業上頗為有利的 黃色反應性染料,本案發明者,經廣泛地研究,找出適合 以上所述萬求的纖維用反應性黃色染料,.發現具有某些特 殊結構的染料组成物,可實現本發明之目的,並將所得結 果陳述於本發明中。 本發明提供一種纖維用反應性黃色染料組成物,其主 要包括下列兩種組成份··(a)由下述式⑴所表示的反應性染 料V. Description of the Invention (Top) In order to obtain a yellow reactive dye with good dye stability and deep dyeing, and which is quite industrially advantageous, the inventor of this case has conducted extensive research to find out the fiber suitable for the above mentioned requirements. Reactive yellow dyes. It was found that dye compositions having certain special structures can achieve the purpose of the present invention, and the results obtained are stated in the present invention. The present invention provides a reactive yellow dye composition for fibers, which mainly includes the following two components ... (a) A reactive dye represented by the following formula ⑴

/ */ *

N—CH2CH20S03H (I) 其中,R!為氫、Cm烷基、Cm氰烷基或C2-4氫氧烷基 硫酸酯;R2、Rs、A及Rs各自獨立分別選自氫、鹵素(氟、 氯、溴或碘)、甲基、乙基、甲氧基或乙氧基;以及(b)由 下列化學式(II)所表示的反應性染料 Υι、 J---------A_wi> Μ------r — 訂-------- (請先閱讀背面之注咅?事項再填寫本頁} 經濟部智慧財產局員工消費合作社印製N—CH2CH20S03H (I) where R! Is hydrogen, Cm alkyl, Cm cyanoalkyl, or C2-4 hydrooxyalkyl sulfate; R2, Rs, A, and Rs are each independently selected from hydrogen, halogen (fluorine, (Chlorine, bromine or iodine), methyl, ethyl, methoxy or ethoxy; and (b) a reactive dye represented by the following chemical formula (II), J --------- A_wi & gt Μ ------ r — Order -------- (Please read the note on the back? Matters before filling out this page} Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs

Ν· -so2ch2ch2oso3h 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 1225508 A7 B7 五、發明説明(3 ) (II) 其中,Υ!及各自獨立分別選自Ci 4烷基或Ci 4烷氧基; 丫3、Y4及Ys各自獨立分別選自氫原子、鹵素(氟、氯、溴 或碘)、甲基或磺酸基。 【發明之具體例詳細説明】 本發明物之染料組成物主要係由組成份(a)之式⑴染料 及組成份(b)之式(II)染料等兩種染料所組成。 式⑴染料的合成方法,可參考美國專利第4,271,072 號中所揭示。 式(II)染料的合成方法,在德國公開專利申請案號 (published patent application No·) 1,150,163 號中有介紹。 使用本發明中式(I)所代表的反應性染料並無特殊限 制’較佳的是如下式(III)所代表的反應性染料: (請先閱讀背面之注意事項再填寫本頁) in VH ϋϋ !1 ϋϋ 该- ί - —T9 iti —^ϋ HI - 訂 經濟部智慧財產局員工消費合作社印製Ν · -so2ch2ch2oso3h This paper size applies to Chinese National Standard (CNS) A4 (210 X 297 mm) 1225508 A7 B7 V. Description of the invention (3) (II) where Υ! And each are independently selected from Ci 4 alkyl Or Ci 4 alkoxy; y 3, Y 4 and Ys are each independently selected from a hydrogen atom, a halogen (fluorine, chlorine, bromine or iodine), a methyl group or a sulfonic acid group. [Detailed description of specific examples of the invention] The dye composition of the present invention is mainly composed of two kinds of dyes, such as the formula VII dye of the component (a) and the dye of the formula (II) of the component (b). For a method of synthesizing the formula VII dye, refer to U.S. Patent No. 4,271,072. A method for synthesizing a dye of formula (II) is described in German published patent application No. 1,150,163. There are no particular restrictions on the use of reactive dyes represented by formula (I) in the present invention. 'Reactive dyes represented by formula (III) are preferred: (Please read the precautions on the back before filling this page) in VH ϋϋ ! 1 ϋϋ This-ί-—T9 iti — ^ ϋ HI-Ordered by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs

/R1 N1H2CH2〇S〇3H 〇 r^VN==N II o (III) 其中 Ri’是-CH/H3 或一 CH2CH2_OS〇3H;R3,是氯原子 氯原子。而更佳的是如下式(M)所代表的反應性染料。 ho3so—ch2—ch2- 本紙張尺度適用中國國家標準(CNS )八4規格( 210X297^ 1225508 A7 B7 發明說明(4) ho3so—ch2—ch2/ R1 N1H2CH2〇S〇3H 〇 r ^ VN == N II o (III) where Ri 'is -CH / H3 or -CH2CH2_OS〇3H; R3 is a chlorine atom chlorine atom. More preferred is a reactive dye represented by the following formula (M). ho3so—ch2—ch2- This paper size is applicable to China National Standard (CNS) eight 4 specifications (210X297 ^ 1225508 A7 B7 Description of invention (4) ho3so—ch2—ch2

N=:nN =: n

CH2CH20S03H N*CH2CH20S03H (M)CH2CH20S03H N * CH2CH20S03H (M)

限制,較佳 (請先閱讀背面之注意· Φ, I事項再 -裝 填寫本頁) ϋ ϋ ϋ^OJI ·ϋ ϋ ϋ n ϋ iai I - 經濟部智慧財產局員工消費合作社印製 (IM) 本發明之染料組成物能藉著各種方法㈣,例如^ 分開配製不同的個別染料,然後將之混合,這混合方法^ 在週合的混合器中進行,例如在顚動筒;或在適當的W 器,例如球和砂碌磨器中發生,但是同樣藉著揽動使它个 成為染料液體而使個別染料混合;或者是在每個染料的邊 備方法中控制反應條件,使在置備的同時產生理想混名Restrictions, better (please read the note on the back, Φ, I, and then fill in this page) ϋ ϋ ϋ ^ OJI · ϋ ϋ ϋ n ϋ iai I-Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs (IM) The dye composition of the present invention can be prepared by various methods, such as ^ preparing different individual dyes separately, and then mixing them. This mixing method ^ is performed in a weekly mixer, such as a joist drum; or in an appropriate W devices, such as balls and sand mills, but also by mixing them into dye liquids to mix individual dyes; or control the reaction conditions in the side-by-side method of each dye, so that Ideal mix name

木紙張尺度適用中國國家標準(CNS)A4規格⑽x 297公爱T 1225508 A7 B7 五、發明説明(S) 智 慧 財 產 局 員 工 消 費Wood paper scale is applicable to Chinese National Standard (CNS) A4 specifications x 297 Public Love T 1225508 A7 B7 V. Description of the invention (S) Employees of Intellectual Property Bureau

物;也可以在浸染或印染的過程中,個別的染料可以彼此 混合。 如有必要,本發明纖維反應性染料中也可以含有盔機 鹽類]例如硫酸鋼、氯化鋼等;分散劑,例如/奈續酸 甲酸縮合產物、甲基奈績酸_甲駿縮合產物、酿胺基奈紛系 化合物等;防塵劑(non_dusting agent),例如對苯二甲酸二 -2-乙基己醋等;pH値緩衝劑,例如乙酸u酸納等: 水軟化劑,例如聚磷酸酯等;或傳統助染劑等。 , 本發明纖維反應性染料組成物之型態並無特殊限制, 也就是可以為粉狀、粒狀或液態。本發明為了説明方便,在説明書中化合物皆以自由酸 的形式表示,但本發明中的染料在被製造或使用時,常备以水溶性鹽㈣式存在,特別是驗金屬鹽,尤其 : 鉀鹽、銨鹽。 風 、本發明黃色反應性染料組成物,適用於對纖維材料, 尤指,維素纖維材料,以及含纖維素纖維纖維材料的 或印花。纖維素纖維材料並無特殊限制,包含天炊 ^維^維,例如純棉纖維、亞麻、大麻、手麻、黏液 累縈’或是含纖維素系纖維的纖維材料。〜,發明之染色或印染可照_般習知、慣用的方法進 :’次染法(exh_icm dyeing)是採用熟知的無機中性 無水硫酸納及氯化納)及熟知的酸結合劑(如碳酸鋼:J 請 先 閲 讀 背 面 之 注It is also possible to mix individual dyes during the process of dip or print. If necessary, the fiber-reactive dyes of the present invention may also contain helmet salts] such as sulfuric acid steel, chlorinated steel, etc .; dispersants, such as / napic acid formic acid condensation products, methyl nalic acid-methyljun condensation products , Amino acid naphthene compounds, etc .; non-dusting agent, such as di-2-ethylhexyl terephthalate, etc .; pH buffering agents, such as sodium acetate u acid, etc .: water softeners, such as polymer Phosphate ester, etc .; or traditional dyeing aids, etc. The type of the fiber-reactive dye composition of the present invention is not particularly limited, that is, it can be powdery, granular, or liquid. For the convenience of explanation, the compounds in the specification are all expressed in the form of free acids. However, when the dyes of the present invention are manufactured or used, they are usually prepared in the form of water-soluble salts, especially metal salts, especially: potassium Salt, ammonium salt. The yellow, reactive dye composition of the present invention is suitable for printing or printing on fiber materials, especially vitamin fiber materials, and cellulose fiber fiber materials. There are no special restrictions on cellulose fiber materials, including natural foods, such as cotton fibers, flax, hemp, hand hemp, mucus accumulates, or fiber materials containing cellulose fibers. ~, The dyeing or printing of the invention can be carried out according to the conventional and customary methods: 'exh_icm dyeing uses the well-known inorganic neutral anhydrous sodium sulfate and sodium chloride) and well-known acid binders (such as Carbonate steel: J Please read the note on the back first

I 奢 裝· 訂 本紙張尺^I Luxury binding and binding paper ruler ^

I 1225508 經濟部智慧財產局員工消費合作社印製 A7 B7 五、發明說明(心) 化鈉)單獨或混合使用。無機中性鹽和鹼的用量並不是很重 要,無機中性鹽和鹼可以依傳統方法一次或分次加入染浴 中 此外,也可以依傳統方法加入助染劑(dyeing assistants)(如均染劑(leveling agents)、緩染劑(retarding agents)等),染色溫度通常是介於4(rc_9〇〇c,較佳的是4〇 〇C-70〇C 〇 冷壓染法(cold batch-up dyeing method)是使欲染色的 物質,利用熟知的無機中性鹽(如無水硫酸鈉及氣化鈉)及 熟知的酸結合劑(如矽酸鈉、氫氧化鈉)軋染,然後在室溫 下’使所得的物質成捲置形式,進行染色。 連績染色法疋卓浴壓染法進行染色,係用熟知的酸結 合劑(如碳酸鈉或碳酸氫鈉)和軋染液混合,依常法使欲染 色之物質進行軋染,然後使所得物質乾熱或汽蒸固色;兩 浴軋染法是以染料使欲染色之物質進行軋染,然後以熟知 的無機中性鹽(如無水硫酸鈉或氯化鈉)及熟知的酸結合劑 (如氫氧化鈉或矽酸鈉)處理,最好依常法將處理過的物質 乾燥或汽蒸固色。 織物印花法(textile printing methods),例如有單相印 花法,係以含有熟知酸結合劑(如碳酸氫鈉)之印花漿, 印在欲印花的物質上,並用乾燥或汽蒸固色;兩相印花法 包含以印花漿欲印花的物質,將所得物質浸入在高溫(9〇 °C或以上)之含無機中性鹽(如氯化鈉)及熟知的酸結合 本紙張尺度適用中國國家標準(CNS)A4規格(21〇 x 297公釐) -I---------裝------^--訂---- (請先閱讀背面之注意事項再填寫本頁) 1225508 五、發明說明( 劑(如氫氧化銷或碎酸鋼)之溶液中固色、、 法並不侷限前列之染色或印花法。 a明之万 本發明組成物對纖維素纖維來講,它是一 値的黃色反應性染料,可以得到各種 :、業貝 性、染色及印染再現性、均染性== :壓染產r好的染液安定性,可得高品質的染色、印染 ㈣=便更進-步説明起見,將列舉以下實施例作更具 訂 以下實施例為本發明之具體m旦不會因此而限定 本發月的範圍’其中化合物是以游離酸的形式表示,但其 實際的形式有可能是金屬鹽,更可能是鹼金屬鹽,尤其: 鋼鹽’除非有特別説明,否則實施例中所使用的份數或百 分比皆以重量為單位,溫度以攝氏溫度。c為單位。 實施例1 取前述之式(1-1)反應性染料35份,與前述之式(11_1} 反應性染料65份,均勻混合而得染料組成物A。 實施例2 取前述之式(1-1)反應性染料22份,與前述之式(II-1) 反應性染料7 8份,均勻混合而得染料組成物b。 本紙張尺度適用中國國家標準(CNS)A4規格(21〇 x 297公釐) 1225508 經濟部智慧財產局員工消費合作社印製 A7 B7 五、發明說明(?) 實施例3 取箾述之式(1-1)反應性染料45份,與前述之式(ικ) 反應性染料55份,均勻混合而得染料組成物c。 比較例1 以100%之式(II-1)反應性染料做為比較染料。為證明 本發明之染料組成物之優異染色效果,以1〇0%之式(π_υ 反應性染料(芫全未添加前述之式(U)反應性染料)做為對 照用比較染料’與本發明之染料組成物一起進行下列各項 染色試驗。 試驗例1.(壓吸蒸處(Pad Dry-Pad Steam)染深特性試驗) 分別以比較例1之式(II-1)反應性染料與本發明實施例 1之染料組成物A,進行壓吸蒸處染深特性試驗,其試驗 步银與域驗結果如下所示。 試驗步驟:調製染色濃度5、10、20、30、40、60克/ 升的染液各100毫升,以全棉絲光斜紋布(12 X 30cm)施染, 將全棉絲光斜紋布浸潰於染液中,讓染料吸附擴散,控制 全棉絲光斜紋布的壓吸率(pick up)為70%,染液溫度維持 在25°C,接著利用ir/hf壓染預乾機進行織物軋液染色, 並將之乾燥,然後加入70%的水玻璃(48GB,e),進行軋液 10 本紙張尺度適用中_家標準(CNS)A4規格(21G X 297公爱) I ϋ H I I ϋ H ϋ n I · l ϋ n ϋ·ϋ ϋ al·、I I I I ϋ ϋ n 1 I . Γ%先閱讀背面之注音?事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 1225508 Α7 ---------_JB7______ 五、發明說明(1 ) 壓吸蒸處(飽和蒸汽40秒),最後將上述染色完成的染色布 經水洗、岂洗、烘乾後,得到完成品。 試驗結果:壓吸蒸處染深特性試驗結果,如下表一所 示。 表一 5 ___染液濃度(克/升) 10 20 30 40 60 式(Π-1)染料 之Σ K/S値 23.45 50.1 84.17 106.71 119.88 128.58 染料組成物A 之Σ K/S値 29.78 54.12 106.09 129.91 145.09 159.33 K/S為庫氏係數(kubelka coefficient ),Σ κ/s値越高者,則 染料的染深性越佳。 表一中,本發明實施例1之染料組成物A之2 κ/S値, 均較比較例1之式(II-1)反應性染料之2K/S値高,例如,染 液濃度同樣為60克/升時,本發明實施例1之染料組成物a 之Σ K/S値為159.33,而比較例1之式(Π-1)反應性染料之芝 K/S値為128.58。此顯示本發明實施例1之染料組成物A其 染深性,比單純使用1〇〇%之式(Π_1)反應性染料者佳。 試驗例2.(冷壓捲染(c.P.B)染深特性試驗) 知比較例1之式(11 -1)反應性染料與貫施例1中染料組 11 参纸張尺度適用中國國家標準(CNS)A4規格(21〇 χ 297公釐) I-----------裝------.—訂--------- (請先閱讀背面之注意事項再填寫本頁) 1225508 A7 B7 五、發明說明(「 成物A分別混合均勻後,進行冷壓捲染(CpB)染色試驗, 其試驗步騾與試驗結果如下所示。試驗步驟:調製染色濃度5、10、2〇、3〇、4〇、6〇克/ 升的染液各80毫升,接著加入20毫升的驗快速混合,驗 劑用量如下表二所示: 鹼劑用量 染液濃度克/升 20 〜40 —~ 40 〜70 70 NaOH(38〇 B,e)用量 毫升/升 15 20 25 30 Na2Si03(48G B’e)用量 克/升 100 (請先閱讀背面之注意事項再填寫本頁) •裝 本 經濟部智慧財產局員工消費合作社印製 用上述染液去染全棉絲光斜紋布(12 X 3〇cm),將布浸 潰於染液中,讓染料吸附擴散,控制全棉絲光斜紋布的壓 吸率(pick up)為70%,染液溫度維持在2yC,接著利用壓 染試色機進行織物軋液染色,然後將軋液完成的染色布於 室溫下捲置4小時,之後再經水洗、包洗、烘乾,最後得 到完成品。 試驗結果:冷壓捲染(C.P.B)染深特性試驗結果,如下 表三及表四所示。 1T*---------擎· 12 1225508 A7 B7 五、發明說明(") 表三:輔丞深姓(Build ut3 Cotton、 染液濃度(克/升) 5 10 20 30 40 60 式(II-1)染料 之Σ K/S値 18.08 33.68 61.58 83.82 98.24 115.68 染料組成物A 之Σ K/S値 18.16 37.51 69.53 93.32 110.68 128.17 K/S為庫氏係數(kubelka coefficient ),Σ K/S値越高者,則 染料的染深性越佳。 __ 表四:碟瞢垫!性(Build ud Ravon、 染液濃度(克/升) 5 10 20 30 40 60 式(Π-1)染料之 Σ K/S 値 20.74 39.99 76.67 97.96 118.67 136.15 染料組成物A 之Σ K/S値 22.5 42.26 79.89 112.08 130.12 154.98 K/S為庫氏係數(kubelka coefficient ),Σ K/S値越高者,則 染料的染深性越佳。 (請先閱讀背面之注意事項再填寫本頁) Λ n ϋ— ϋ ϋ_ι ϋ— ϋ ^ I ϋ·1 ικι_1 tmt im 經濟部智慧財產局員工消費合作钍印製 表三及表四中,本發明實施例1之染料組成物A之2:K/S 値,均較比較例1之式(IM)反應性染料之2K/S値高。此顯 示本發明實施例1之染料組成物A其冷壓捲染(C P B)染深 特性’比單純使用100%之式(11_丨)反應性染料者為佳。 試驗例三·(捲置時間依存性試驗) 13I 1225508 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs A7 B7 V. Description of Invention (Heart Sodium Sulfide) Use alone or in combination. The amount of the inorganic neutral salt and alkali is not very important. The inorganic neutral salt and alkali can be added to the dyeing bath one or more times according to the traditional method. In addition, dyeing assistants (such as uniform dyeing) can also be added according to the traditional method. Leveling agents, retarding agents, etc.), the dyeing temperature is usually between 4 (rc_90 ° c, preferably 400 ° C-70 ° C, cold batch- Up dyeing method) is to dye the substance to be dyed, using well-known inorganic neutral salts (such as anhydrous sodium sulfate and sodium gasification) and well-known acid binding agents (such as sodium silicate, sodium hydroxide) padding, and then in the room The resulting material is rolled at a temperature to be dyed in a roll form. The continuous dyeing method is performed using a bath-bath pressure dyeing method, which is mixed with a well-known acid binder (such as sodium carbonate or sodium bicarbonate) and a padding solution. The material to be dyed is pad dyed according to the usual method, and then the obtained material is dry-heated or steam-fixed; the two-bath pad dyeing method is used to pad dye the substance to be dyed, and then the well-known inorganic neutral salt ( (Such as anhydrous sodium sulfate or sodium chloride) and well-known acid binding (Such as sodium hydroxide or sodium silicate) treatment, it is best to dry or steam fix the treated material in accordance with conventional methods. Textile printing methods, such as single-phase printing methods, contain well-known acids The printing paste of a binding agent (such as sodium bicarbonate) is printed on the substance to be printed, and the color is fixed by drying or steaming; the two-phase printing method includes the substance to be printed with the printing paste, and the obtained substance is immersed in a high temperature (9 °). ° C or above) containing inorganic neutral salts (such as sodium chloride) and well-known acids combined with this paper standard applicable to China National Standard (CNS) A4 specifications (21 × 297 mm) -I ------ --- Pack -------- ^-Order ---- (Please read the precautions on the back before filling this page) 1225508 V. Description of the invention (agent (such as hydroxide pin or broken acid steel) solution The medium-fixing method is not limited to the forefront dyeing or printing methods. A Mingzhiwan For the cellulose fiber, it is a stack of yellow reactive dyes, which can obtain a variety of: And printing and dyeing reproducibility and leveling property ==: good stability of dyeing solution produced by pressure dyeing, can obtain high-quality dyeing Printing and dyeing ㈣ = will be further-for the sake of explanation, the following examples will be enumerated for further customization. The following examples are specific to the present invention and will not limit the scope of the present month. 'Where the compound is a free acid The form is expressed, but the actual form may be a metal salt, more likely an alkali metal salt, in particular: Steel salt 'Unless otherwise specified, the parts or percentages used in the examples are by weight, and the temperature is The temperature is in Celsius. The unit is c. Example 1 35 parts of the reactive dye of the formula (1-1) and 65 parts of the reactive dye of the formula (11_1) were uniformly mixed to obtain the dye composition A. Example 2 Take 22 parts of the reactive dye of the formula (1-1), and 78 parts of the reactive dye of the formula (II-1), and uniformly mix to obtain a dye composition b. This paper size applies the Chinese National Standard (CNS) A4 specification (21 × 297 mm) 1225508 Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs A7 B7 V. Description of the invention (?) Example 3 Take the formula (1) -1) 45 parts of a reactive dye and 55 parts of a reactive dye of the formula (ικ) are uniformly mixed to obtain a dye composition c. Comparative Example 1 A 100% reactive dye of formula (II-1) was used as a comparative dye. In order to prove the excellent dyeing effect of the dye composition of the present invention, a comparison dye of 100% formula (π_υ reactive dye (without the addition of the aforementioned formula (U) reactive dye) is used as a control) is compared with the present invention. The dye composition was subjected to the following dyeing tests together. Test Example 1. (Pad Dry-Pad Steam Dye Depth Test) The reactive dye of formula (II-1) of Comparative Example 1 The dye composition A of Inventive Example 1 was subjected to a pressure-sucking-dyeing depth characteristic test, and the test results of silver and field test results are shown below. Test steps: Adjust the dyeing concentration to 5, 10, 20, 30, 40, 60 g / Liter of dyeing solution 100 ml each, dyed with cotton mercerized twill (12 X 30cm), immerse the cotton mercerized twill in the dyeing solution, let the dye adsorb and diffuse, and control the pressure absorption of cotton mercerized twill (pick up) is 70%, the temperature of the dyeing solution is maintained at 25 ° C, then the fabric rolling solution is dyed with an ir / hf pressure dyeing pre-dryer, and then dried, and then 70% water glass (48GB, e) is added for Rolling liquid 10 This paper size is applicable _ house standard (CNS) A4 specification (21G X 297 male ) I ϋ HII ϋ H ϋ n I · l ϋ n ϋ · ϋ ϋ al ·, IIII ϋ 1 n 1 I. Γ% Read the note on the back? Matters and then fill out this page) Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs System 1225508 Α7 ---------_ JB7______ V. Description of the invention (1) Pressure suction (saturated steam for 40 seconds). Finally, the dyed cloth is washed, washed and dried to obtain Finished goods. Test results: The results of the test of the dyeing depth at the pressure suction position are shown in Table 1 below. Table 1 ___ Concentration of dyeing solution (g / l) 10 20 30 40 60 Σ K / S 値 of formula (Π-1) dye 23.45 50.1 84.17 106.71 119.88 128.58 Σ K / S 値 29.78 54.12 106.09 of dye composition A 129.91 145.09 159.33 K / S is the kubelka coefficient. The higher the Σ κ / s 値, the better the deepness of the dye. In Table 1, the 2 κ / S 値 of the dye composition A of Example 1 of the present invention is higher than the 2K / S 反应 of the reactive dye of formula (II-1) in Comparative Example 1. For example, the concentration of the dye solution is also At 60 g / l, the Σ K / S 値 of the dye composition a of Example 1 of the present invention is 159.33, and the K / S 芝 of the reactive dye of the formula (Π-1) of Comparative Example 1 is 128.58. This shows that the dye composition A of Example 1 of the present invention has a deeper dyeing property than that using only 100% of the reactive dye of the formula (Π_1). Test Example 2. (CPB) Dyeing Deepness Test Knowing the formula (11 -1) in Comparative Example 1 and the reactive dyes and dye groups in Example 1 of the 11 reference paper standards are applicable to Chinese national standards (CNS ) A4 size (21〇χ 297 mm) I ----------- install ------.-- order --------- (Please read the precautions on the back first Fill out this page again) 1225508 A7 B7 V. Description of the invention ("After the product A has been mixed uniformly, a cold press dyeing (CpB) dyeing test is performed. The test steps and test results are shown below. Test steps: adjust the dyeing concentration 80 ml each of 5, 10, 20, 30, 40, 60 g / L dye solution, and then add 20 ml of test solution for rapid mixing. The dosage of test agent is shown in Table II below. / Liter 20 ~ 40 — ~ 40 ~ 70 70 NaOH (38〇B, e) dosage ml / liter 15 20 25 30 Na2Si03 (48G B'e) dosage g / liter 100 (Please read the precautions on the back before filling in this Page) • Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs to print cotton mercerized twill (12 X 30cm) with the above dyeing solution, immerse the cloth in the dyeing solution to allow the dye to absorb and diffuse. The cotton cotton mercerized twill fabric has a pick-up rate of 70%, the dyeing solution temperature is maintained at 2yC, and then the dyeing test machine is used to dye the fabric rolling solution, and then the finished dyed fabric is rolled at room temperature. After being left for 4 hours, the finished product is finally washed, washed, and dried. Test results: The results of the deep test of CPB are shown in Tables 3 and 4 below. 1T * --- ------ Qing · 12 1225508 A7 B7 V. Description of the invention Table III: Auxiliary name (Build ut3 Cotton, Dye concentration (g / L) 5 10 20 30 40 60 Formula (II- 1) Σ K / S 値 18.08 33.68 61.58 83.82 98.24 115.68 Σ K / S 値 18.16 37.51 69.53 93.32 110.68 128.17 K / S is the kubelka coefficient, the higher the Σ K / SΣ The better the deepness of the dye. __ Table 4: Dish mat! Properties (Build ud Ravon, concentration of dye solution (g / l) 5 10 20 30 40 60 Σ K / of the formula (Π-1) dye S 値 20.74 39.99 76.67 97.96 118.67 136.15 Σ K / S of dye composition A 22.5 42.26 79.89 112.08 130.12 154.98 K / S is S coefficients (kubelka coefficient), Σ K / S Zhi were higher, the better the deep dyeing dye. (Please read the precautions on the back before filling this page) Λ n ϋ— ϋ ι_ι ϋ— ϋ ^ I ϋ · 1 ικι_1 tmt im Employees ’Cooperative Cooperation with Intellectual Property Bureau of the Ministry of Economy The dye composition A of Example 1 2: K / S 値 is higher than the 2K / S 値 of the reactive dye of formula (IM) of Comparative Example 1. This shows that the dye composition A of Example 1 of the present invention has better cold press dyeing (C P B) dyeing characteristics ′ than the one using only 100% of the reactive dye of the formula (11_ 丨). Test example three (rolling time dependency test) 13

1225508 A7 B7 五、發明説明(p ) 分別以比較例i之式(Π-1)反應性染料與本發明實施例 1之染料組成物A,進行捲置時間依存性試驗,其試驗步 驟與試驗結果如下所示。 試驗步驟··調製染色濃度30克/升的染液各16〇毫升, 接著加入40毫升的鹼快速混合,鹼劑用量如下所示: NaOH ( 38° B?e ) 20 毫升/升1225508 A7 B7 V. Description of the invention (p) Reel time dependency test was performed using the reactive dye of formula (Π-1) of Comparative Example i and the dye composition A of Example 1 of the present invention, and the test steps and tests The results are shown below. Test procedure ... Make a dyeing solution with a concentration of 30 g / L of 160 ml each, and then add 40 ml of alkali for rapid mixing. The amount of alkaline agent is as follows: NaOH (38 ° B? E) 20 ml / L

Na2Si〇3 ( 48°B5e) 100 克/升 用上述染液去染全棉絲光斜紋布(12 X 30cm ),將布 反潰於染液中,讓染料吸附擴散,控制全棉絲光斜紋布的 壓吸率(pick up)為70%,染液溫度維持在25。〇,接著利用 壓染試色機進行織物軋液染色,然後將軋染完成的染色布 於 35C 下依序捲置 1、2、3、4、6、8、1〇、12、16、24、 32、48小時,之後再經水洗、色洗、烘乾,最後得到完成 品。 试驗結果·捲置時間依存性試驗結果,如下表五所示。 (請先閲讀背面之注意事項再填寫本頁) >裝· t· 經濟部智慧財產局員工消費合作社印製 捲置時間(Batch time)(時) 1 2 3 4 6 8 10 12 16 24 32 48 式(IM)染料 之染色相對力 度 97 103 103 103 105 101 101 100 99 100 97 94 染料組成物 A之染色相 對力度 99 102 101 103 102 100 99 99 100 100 97 96 將式(II-1)染料及染料組成物A,染色所得之染色布, 14 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 1225508 經濟部智慧財產局員工消費合作社印製 A7 五、發明說明(6 ) 使用DATA MATCH電腦測色系統比較染色力度變化差異, 以捲置24小時為相對標準(1〇〇),試其各時點的染色相對 力度’交化越接近者越佳。表五中,本發明實施例丨之染料 組成物A之各時點的染色相對力度變化,均較比較例丨之 式(Π-1)反應性染料之染色相對力度變化更接近1〇〇。此顯 示本發明實施例1之染料組成物A其比單純使用1〇〇%之 式(II-1)反應性染料者佳。 試驗例四·(蒸處時間依存性試驗) 为別以比較例1之式(H-1)反應性染料與本發明實施例 1足染料組成物A,進行蒸處時間依存性試驗,其試驗步 驟與試驗結果如下所示。 4¾步驟·凋製染色濃度3〇克/升的染液各2⑼毫升, 去染全棉絲光斜紋布(12x3〇cm),將布浸潰於染液中, 讓染料吸附擴散,控制全棉絲光斜紋布的壓吸率叩) 為70%,染液溫度維持在25τ,接著利用ir/hf壓染預 乾機進行織物軋液染色並乾燥之。將驗劑倒人乾燥完成的 中間染色物中,驗劑(A)、(B)及(C)之成分及用量如 下所示: 鹼劑(A) · NaOH ( 3 8GB’e) 14 毫升/升 + Na2c〇3l〇 克/升 +Na2Si〇3 (48 ° B5e) 100 g / l Use the above dyeing solution to dye the cotton mercerized twill (12 X 30cm). The cloth will be immersed in the dyeing solution to allow the dye to adsorb and diffuse and control the pressure absorption of the cotton mercerized twill. The pick up rate was 70% and the temperature of the dye solution was maintained at 25. 〇, then use the dyeing test machine for fabric rolling solution dyeing, and then roll the dyed cloth at 35C in order, roll 1, 2, 3, 4, 6, 8, 10, 12, 16, 24 , 32, 48 hours, and then water washing, color washing, and drying, and finally finished products are obtained. The test results and roll time dependency test results are shown in Table 5 below. (Please read the precautions on the back before filling out this page) > Loading · t · Print time (hours) printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 1 2 3 4 6 8 10 12 16 24 32 48 Relative dyeing strength of formula (IM) dye 97 103 103 103 105 101 101 100 99 100 97 94 Relative dyeing strength of dye composition A 99 102 101 103 102 100 99 99 100 100 97 96 And dye composition A, dyed dyed cloth, 14 paper sizes are applicable to Chinese National Standard (CNS) A4 specifications (210X297 mm) 1225508 Printed by A7, Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs, 5. Description of invention (6) Use The DATA MATCH computer color measurement system compares the difference in dyeing strength. Taking the 24 hours of rolling as the relative standard (100), the closer the relative dyeing strength at each time point is, the better. In Table 5, the change in the relative intensity of the dyeing at each time point of the dye composition A of Example 丨 of the present invention is closer to 100 than that of the reactive dye of the formula (Π-1) of the comparative example. This shows that the dye composition A of Example 1 of the present invention is better than the one using only 100% of the reactive dye of the formula (II-1). Test Example 4 (Steaming Time Dependence Test) The steaming time dependence test was performed using the reactive dye of formula (H-1) of Comparative Example 1 and the dye composition A of Example 1 of the present invention. The steps and test results are shown below. Step 4¾ · Withdraw 2⑼ml each of the dyeing solution with a concentration of 30g / L, and then dye the cotton mercerized twill (12x30cm), soak the cloth in the dyeing solution, let the dye adsorb and diffuse, and control the cotton mercerized twill The pressure absorption rate 叩) is 70%, the temperature of the dyeing solution is maintained at 25τ, and then the fabric rolling solution is dyed with an ir / hf pressure dyeing predryer and dried. Pour the test reagent into the dried intermediate dye. The composition and dosage of the test reagents (A), (B), and (C) are as follows: Alkali (A) · NaOH (3 8GB'e) 14 ml / Liter + Na2c03l / g +

Na2SO4250 克 /升。 鹼劑(Β): _Η(38〇Β,〇 15 毫升/升+ΝΜ〇425〇 克 /升。 T---------裝--------訂--------- (請先閱讀背面之注意事項再填寫本頁) 15 1225508 A7Na2SO4250 g / l. Alkali agent (B): _Η (38〇Β, 015 ml / L + NM〇4250 g / L. T --------- pack -------- order ---- ----- (Please read the notes on the back before filling this page) 15 1225508 A7

五、發明說明(舛) 驗劑(C) : Na2Si03 ( 48❹ B,e) 70% 。 最後再進行軋液壓吸蒸處。蒸處條件:飽和蒸汽乂 2〇、30、40、50、60、70、80、90秒,最後再將上述染色 完成的染色布經水洗包洗烘乾之後,得到完成品。 試驗結果:捲置時間依存性試驗結果,使用鹼劑(A ) 至(C)所得之結果如下表六至八所示。 ϋ ϋ I n I I n l ϋ I » I n ϋ I -n I .^1 一 δ,I n i n I ϋ ϋ ϋ I Λ (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 16 表六 蒸處時間(Steam time)(秒) 20 30 40 50 60 70 80 90 式(IM) 染料之染 色相對力 度 99.50 100.3 100.0 95.72 96.04 95.12 98.80 95.11 染料組成 物A之 染色相對 力度 99.10 100.4 100.0 99.33 99.63 99.49 99.43 99.19 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 1225508 A7 B7 五、發明說明( 表七 蒸處時間(Steam time)(秒) 20 30 40 50 60 70 80 90 式(Π-1) 染料之染 色相對力 度 100.3 100.9 100.0 96.78 97.64 96.61 98.46 97.34 染料組成 物A之 染色相對 力度 98.46 100.1 100.0 100.8 98.61 97.16 98.06 98.0 -n H ϋ ϋ n I I n n n I Λ I 1 (請先閱讀背面之注意事項再填寫本頁) 表八 蒸處時間(Steam time)(秒) 20 30 40 50 60 70 80 90 式(Π-1) 染料之染 色相對力 度 99.30 100.3 100.0 100.7 101.6 98.50 99.05 97.06 染料組成 物A之 染色相對 力度 100.9 101.5 100.0 101.3 101.8 101.5 99.75 99.24 訂 將式(π-1)反應性染料及染料組成物A,染色所得之染 色布,使用DATA MATCH電腦測色系統比較染色力度的 差異變化,各以蒸處40秒為相對標準,試其各點的相對 力度變化越接近者越佳。表六至八所示中,本發明實施例 1之染料組成物A之整體的的染色相對力度變化,較比較 17 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公爱) 1225508 A7 B7 五、發明說明(屮) 例1之式(II-1)反應性染料之染色相對力度變化小。此顯示 本發明實施例1之染料組成物A其比單純使用100%之式 (II-1)反應性染料者佳。 試驗例五·(日光堅牢度試驗) 分別以比較例1之式(II-1)反應性染料與本發明實施例 1之染料组成物A,進行日光堅牢度試驗,其試驗步騾與 試驗結果如下所示。 試驗步驟:將實施例中式反應性染料及染料組成 物A分別混合均勻後進行c.p.b染色試驗。 調製染色濃度10、3〇、6〇克/升的染液各80毫升,接 著加入20毫升的鹼快速混合,鹼劑用量如下表所示 表九 鹼劑用量 染液濃度克/升 20 20 〜40 40 〜70 70 NaOH ( 38〇 B,e )用量 毫升/升 15 20 25 30 Na2Si03 ( 48〇 B’e )用量 克/升 100 用上述染液去染全棉絲光斜紋布(12 X 3 0cm ),將布 浸潰於染液中,讓染料吸附擴散,控制全棉絲光斜紋布的 18 本紙張尺度卿中國國家標#(CNS)A4規格(210 (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泎杜印裂 297公釐) 1225508 A7 ___B7_ 五、發明說明(Π) (請先閱讀背面之注意事項再填寫本頁) 壓吸率(pick up)為70%,染液溫度維持在25°C,接著利用 壓染試色機進行織物軋液染色,然後將軋液完成的染色布 於室溫下捲置4小時,之後再經水洗、良洗、烘乾,最後 4于到冗成品。 將上述染色完成的纖物進行Xenon-Arc Lamp Light (AATCC 16E 1989 )連續施以40AFU的照射試驗。 試驗結果:日光堅牢度試驗結果,如下表十所示。 表十 染色濃度 10克/升 30克/升 60克/升 ISO AATCC ISO AATCC ISO AATCC 式(II-1)染料 之變化級數 2 2-3 2 2 2-3 2-3 染料組成物A 之變化級數 2-3 2-3 3 3-4 4 4-5 將式(II-1)反應性染料及染料組成物A,染色所得之染 色布,經照射測試後,使用DATA MATCH電腦測色系統 比較試驗前後的染色力度差異,變化級數較高者為佳。本 發明實施例1之染料組成物A之變化級數,均較比較例1 之式(II-1)反應性染料之變化級數更高。此顯示本發明實施 例1之染料組成物A其比單純使用100%之式(II-1)反應性 19 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 1225508 A7 B7 五、發明說明(丨Π 染料者佳。 試驗例六·(耐水洗堅牢度試驗) 分別以比較例1之式(ΙΙ-1)反應性染料與本發明實施例 1之染料組成物A,進行耐水洗堅牢度試,其試驗步騾與 武驗結果如下所示。 試驗步驟:調製染色濃度30克/升的染液各8〇毫升, 接著加入20毫升的鹼快速混合,鹼劑用量如下所示: NaOH ( 38〇B’e) 20 毫升 / 升V. Description of the invention (i) Test reagent (C): Na2Si03 (48❹ B, e) 70%. Finally, the rolling hydraulic suction is performed. Steaming conditions: saturated steam 乂 20, 30, 40, 50, 60, 70, 80, 90 seconds, and finally washing and drying the dyed cloth after dyeing to obtain a finished product. Test results: The results of the coiling time dependence test. The results obtained by using the alkaline agents (A) to (C) are shown in Tables 6 to 8 below. ϋ ϋ I n II nl ϋ I »I n ϋ I -n I. ^ 1 One δ, I nin I ϋ ϋ ϋ I Λ (Please read the precautions on the back before filling out this page) Staff Consumption of Intellectual Property Bureau, Ministry of Economic Affairs Cooperative printed 16 Table 6 Steam time (seconds) 20 30 40 50 60 70 80 90 Formula (IM) Relative dyeing strength of dye 99.50 100.3 100.0 95.72 96.04 95.12 98.80 95.11 Relative dyeing strength of dye composition A 99.10 100.4 100.0 99.33 99.63 99.49 99.43 99.19 This paper size is applicable to China National Standard (CNS) A4 (210 X 297 mm) 1225508 A7 B7 V. Description of the invention (Table 7 Steam time (seconds) 20 30 40 50 60 70 80 90 Formula (Π-1) Relative dyeing strength of dyes 100.3 100.9 100.0 96.78 97.64 96.61 98.46 97.34 Relative dyeing strength of dye composition A 98.46 100.1 100.0 100.8 98.61 97.16 98.06 98.0 -n H ϋ ϋ n II nnn I Λ I 1 (Please read the notes on the back before filling this page) Table 8 Steam time (seconds) 20 30 40 50 60 70 80 90 Formula (Π-1) Relative dyeing strength of dyes 99.30 100.3 100.0 100.7 101.6 98.50 99.05 97.06 Relative dyeing strength of dye composition A 100.9 101.5 100.0 101.3 101.8 101.5 99.75 99.24 The formula (π-1) reactive dye and dye composition A shall be determined. The dyed cloth obtained by dyeing shall be measured by DATA MATCH computer The differences in dyeing strength are compared systematically, each taking the steaming place as a relative standard for 40 seconds, and the closer the relative strength change at each point is, the better. The dye composition A of Example 1 of the present invention is shown in Tables 6 to 8. The overall strength of the relative dyeing changes, compared with 17 paper sizes. The Chinese national standard (CNS) A4 specification (210 X 297 public love) is applied. 1225508 A7 B7 V. Description of the invention (屮) Example 1 formula (II-1) The dyeing relative strength of the reactive dye changes little. This shows that the dye composition A of Example 1 of the present invention is better than the one using only 100% of the reactive dye of formula (II-1). Test Example 5 (Sunlight fastness test) The sunlight fastness test was performed with the reactive dye of formula (II-1) of Comparative Example 1 and the dye composition A of Example 1 of the present invention, and the test steps and test results were performed. As follows. Test procedure: The reactive dyes and dye composition A of the formula in the examples are mixed uniformly and then the c.p.b dyeing test is performed. Prepare 80 ml of dyeing solution with a dyeing concentration of 10, 30, and 60 g / liter, and then add 20 ml of alkali to mix quickly. The amount of alkali agent is shown in the table below. 40 40 ~ 70 70 NaOH (38〇B, e) dosage ml / L 15 20 25 30 Na2Si03 (48〇B'e) dosage g / liter 100 Use the above dyeing solution to dye cotton mercerized twill (12 X 3 0cm) , Immerse the cloth in the dye solution, let the dye absorb and diffuse, and control the 18 paper sizes of the cotton mercerized twill cloth China National Standard # (CNS) A4 specifications (210 (please read the precautions on the back before filling this page) Order --------- Consumption of Employees of Intellectual Property Bureau of the Ministry of Economic Affairs, Du Yinye 297 mm) 1225508 A7 ___B7_ V. Description of Invention (Π) (Please read the precautions on the back before filling this page) Press The pick-up rate is 70%, the temperature of the dyeing solution is maintained at 25 ° C, then the fabric is dyed with a press dyeing tester, and then the dyed cloth finished with the solution is rolled at room temperature for 4 hours. After water washing, good washing, and drying, the final product is 4 to redundant. The dyed fibrous material was subjected to an irradiation test of Xenon-Arc Lamp Light (AATCC 16E 1989) and continuously subjected to 40 AFU. Test results: The results of the sunlight fastness test are shown in Table 10 below. Table 10 Dyeing concentration of 10 g / l 30 g / l 60 g / l ISO AATCC ISO AATCC ISO AATCC Formula (II-1) Dye Change Order 2 2-3 2 2 2-3 2-3 Dye Composition A Order of change 2-3 2-3 3 3-4 4 4-5 The dyeing cloth obtained by dyeing the reactive dye of formula (II-1) and the dye composition A, after the irradiation test, use a DATA MATCH computer to measure the color The difference in staining intensity before and after the test is systematically compared, and the higher the change order is, the better. The order of change of the dye composition A of Example 1 of the present invention is higher than that of the reactive dye of formula (II-1) of Comparative Example 1. This shows that the dye composition A of Example 1 of the present invention is 100% more reactive than the formula (II-1). 19 This paper size is applicable to China National Standard (CNS) A4 specifications (210 X 297 mm) 1225508 A7 B7 5. Description of the invention (丨 Π dyes are preferred. Test Example 6 (washing fastness test) Reactive dyes of formula (III-1) of Comparative Example 1 and the dye composition A of Example 1 of the present invention were carried out respectively. The test results of washing fastness are as follows. The test steps and test results are shown below. Test steps: Prepare 80 ml of each dyeing solution with a concentration of 30 g / L, and then add 20 ml of alkali for rapid mixing. Indication: NaOH (38〇B'e) 20 ml / L

Na2Si03 ( 48°B5e) 100 克/升 用上述染液去染全棉絲光斜紋布(12 X 3〇crn ),將布 次潰於染液中,讓染料吸附擴散,控制全棉絲光斜紋布的 壓吸率(pick up)為70%,染液溫度維持在25°C,接著利用 壓染試色機進行織物軋液染色,然後將軋液完成的染色布 於室溫下捲置4小時,之後再經水洗、皂洗、烘乾,最後 得到完成品。 將上述染色完成的纖物進行AATCC 61 II A耐水洗堅 牢度試驗。 試驗結果:耐水洗堅牢度試驗結果,如下表十一所示。 20 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公爱) ϋ ϋ ϋ n I I n I I · n ϋ (請先閱讀背面之注意事項再填寫本頁) 訂: 1225508 A7 B7 五、發明說明(β 表Η— 顏色變化 ISO AATCC 式(ΙΙ-1)染料之 4-5 4-5 變化級數 染料組成物Α之 4-5 5 變化級數 (請先閱讀背面之注意事項再填寫本頁) 將式(II-l)染料及染料組成物A,染色所得之染色布, 經照射測試後,使用DATA MATCH電腦測色系統比較試 •驗前後的染色力度差異,變化級數較高者為佳。 本發明實施例2之染料組成物B及實施例3之染料組 成物C,可以參考前述試驗例一至六之程序為試驗,亦顯 示其比單純使用100%之式(II-1)反應性染料者佳。 經濟部智慧財產局員工消費合作社印製 本發明之染料組成物是一種通用型的反應性黃色染料 組成物,可適用纖維素纖維染色,其所使用的染色方法為 一般反應性染料染色時所使用的方法,例如,浸染、印染 或連續染色。而具有很特別的優良特性。 本發明所描述的反應性黃色染料組成物是一個具有產 業價値的反應性染料,可以得到各種染色特性良好的染 物,尤其在染深性、耐日光堅牢度、耐水洗堅牢度及均染 性上都有非常優異的表現。 21 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)Na2Si03 (48 ° B5e) 100 g / l Use the above dyeing solution to dye the cotton mercerized twill (12 X 3〇crn). The cloth is immersed in the dyeing solution to allow the dye to adsorb and diffuse and control the pressure absorption of the cotton mercerized twill. The pick-up rate is 70%, the temperature of the dyeing solution is maintained at 25 ° C, and then the fabric rolling solution is dyed with a pressure dyeing test machine, and then the dyed cloth completed by the rolling solution is rolled at room temperature for 4 hours, and then After washing, soaping and drying, the finished product is finally obtained. The dyed fibrous material was subjected to the AATCC 61 II A washing fastness test. Test results: The test results of the fastness to washing are shown in Table 11 below. 20 This paper size applies to China National Standard (CNS) A4 (210 X 297 public love) ϋ ϋ ϋ n II n II · n ϋ (Please read the precautions on the back before filling this page) Order: 1225508 A7 B7 V. Description of the invention (β Table Η-Color change ISO AATCC formula (III-1) 4-5 4-5 Change order Dye composition A-4-5 5 Change order (Please read the precautions on the back before filling This page) After dyeing the dyeing cloth of formula (II-l) and dye composition A, the dyed cloth is subjected to the irradiation test, and the DATA MATCH computer color measurement system is used to compare the test. The dyeing strength before and after the test is different, and the order of change is high. The dye composition B of Example 2 and the dye composition C of Example 3 of the present invention can be tested by referring to the procedures of Test Examples 1 to 6 above, and it is also shown that the ratio is more than 100% using the formula (II-1 Reactive dyes are preferred. The dye composition printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs is a general-purpose reactive yellow dye composition suitable for cellulose fiber dyeing. The dyeing method used is general Reactive dye The method used in the dyeing, for example, dip dyeing, printing or continuous dyeing. It has very excellent characteristics. The reactive yellow dye composition described in the present invention is a reactive dye with industrial price, and can obtain various dyeing characteristics. Good dyeing, especially in terms of deepness, fastness to light, fastness to washing, and leveling. 21 This paper is sized for China National Standard (CNS) A4 (210 X 297 mm) )

Claims (1)

D8 1225508 ^ ίσ 年2月/^曰修正A8 第88115229號,93年2月修正頁 g 六、申請專利範圍 1. 一種反應性黃色染料組成物,包含: (a)如式(1-1)所示之化合物: 請 HO3SO-CH2—D8 1225508 ^ ίσ / February, Amendment A8 No. 88115229, Amendment Page, February 1993 g. Application for Patent Scope 1. A reactive yellow dye composition, including: (a) Formula (1-1) Compound shown: Please HO3SO-CH2— /OtOfeOSCbH N——CH2CH2OSO3H α (1-1) 以及 閱 背 面 之 注 意 事 項 再 填 寫 頁 (b)如式(ΙΙ-1)所示之化合物/ OtOfeOSCbH N——CH2CH2OSO3H α (1-1) and the notes on the back, then fill in the page (b) The compound shown by the formula (III-1) so2ch2ch2oso3h so3h 經濟部智慧財產局員工消費合作社印¾ (Π-1) 其中式(1-1)染料和式(II-1)染料之重量比例為15〜50: 50〜85。 22 本紙張尺度適用中0國家標準(CNS)A4規格(210 X 297公釐)so2ch2ch2oso3h so3h Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economy (Π-1) where the weight ratio of the dye of formula (1-1) and the dye of formula (II-1) is 15 ~ 50: 50 ~ 85. 22 This paper size applies to the Chinese National Standard (CNS) A4 specification (210 X 297 mm)
TW88115229A 1999-09-03 1999-09-03 Yellow reactive dye composition TWI225508B (en)

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