KR20050034437A - Reactive navyblue dyestuff composition - Google Patents

Reactive navyblue dyestuff composition Download PDF

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KR20050034437A
KR20050034437A KR1020030070351A KR20030070351A KR20050034437A KR 20050034437 A KR20050034437 A KR 20050034437A KR 1020030070351 A KR1020030070351 A KR 1020030070351A KR 20030070351 A KR20030070351 A KR 20030070351A KR 20050034437 A KR20050034437 A KR 20050034437A
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group
general formula
dye
compound represented
weight
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백종환
윤석영
한창호
이형숙
김영로
김은주
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이화산업 주식회사
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0033Blends of pigments; Mixtured crystals; Solid solutions
    • C09B67/0046Mixtures of two or more azo dyes
    • C09B67/0055Mixtures of two or more disazo dyes
    • C09B67/0057Mixtures of two or more reactive disazo dyes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/002Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the linkage of the reactive group being alternatively specified
    • C09B62/006Azodyes
    • C09B62/01Disazo or polyazo dyes

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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Abstract

본 발명은 다음 일반식[I]로 표시되는 화합물 30∼80 중량%와 다음 일반식[Ⅱ]로 표시되는 화합물 10∼50 중량% 및 다음 일반식 [Ⅲ]으로 표시되는 화합물 10∼50 중량%를 혼합하여서 조성된 반응성 청색염료 조성물에 관한 것이다.The present invention provides 30 to 80% by weight of the compound represented by the following general formula [I], 10 to 50% by weight of the compound represented by the following general formula [II] and 10 to 50% by weight of the compound represented by the following general formula [III] It relates to a reactive blue dye composition formed by mixing.

` ----- [Ⅰ]` ----- [Ⅰ]

----- [Ⅱ] ----- [Ⅱ]

----- [Ⅲ] ----- [Ⅲ]

상기 식들에서, A는 다음 일반식[A-1] 또는 [A-2]로 표시되는 벤젠 또는 나프탈렌계 아민 화합물이고, R1, R2, R3는 수소, 메틸기, 에틸기, 메톡시기, 에톡시기, 카르복실기, 히드록실기 또는 설폰기이고, R4, R5는 수소, 메틸기, 에틸기, 메톡시기, 에톡시기, 히드록실기 또는 클로로기이고 X는 -CH2CH2OSO3H, -CH 2CH2SSO3H 또는 -CH2=CH2 이고 n은 0∼2인 정수이다.In the above formulas, A is a benzene or naphthalene amine compound represented by the following general formula [A-1] or [A-2], and R 1, R 2 , R 3 are hydrogen, methyl group, ethyl group, methoxy group, ethoxy A time period, a carboxyl group, a hydroxyl group or a sulfone group, R 4 , R 5 are hydrogen, a methyl group, an ethyl group, a methoxy group, an ethoxy group, a hydroxyl group or a chloro group and X is -CH 2 CH 2 OSO 3 H, -CH 2 CH 2 SSO 3 H or —CH 2 = CH 2 and n is an integer from 0 to 2 .

----- [A-1] ----- [A-1]

----- [A-2] ----- [A-2]

Description

반응성 청색 염료 조성물 {Reactive navyblue dyestuff composition}Reactive navyblue dyestuff composition

본 발명은 셀룰로오즈, 셀룰로오즈/나일론 등과 같은 면직물 또는 면혼방직물을 청색으로 염색하기에 적합한 반응성 청색 염료 조성물에 관한 것이다. 구체적으로는 다음 일반식[I]로 표시되는 화합물 30∼80중량%와 다음 일반식[Ⅱ]로 표시되는 화합물 10∼50 중량% 및 다음 일반식[Ⅲ]으로 표시되는 화합물 10∼50 중량%를 혼합하여서 조성된 반응성 청색염료 조성물에 관한 것이다. 본 발명의 염료조성물은 염색시 동일농도의 타염료에 비해서 매우 심도있는 청색을 나타내고, 콜드패드 염색시 알칼리에 대한 안정성이 우수하고, 균염성과 제반견뢰도가 뛰어나며, 타섬유에 대한 오염성이 적고, 빌드업(Build-up)성이 우수한 특성을 갖는다.The present invention relates to reactive blue dye compositions suitable for dyeing cotton or cotton blended fabrics such as cellulose, cellulose / nylon and the like in blue. Specifically, 30 to 80% by weight of the compound represented by the following general formula [I], 10 to 50% by weight of the compound represented by the following general formula [II] and 10 to 50% by weight of the compound represented by the following general formula [III] It relates to a reactive blue dye composition formed by mixing. The dye composition of the present invention has a very deep blue color compared to other dyes of the same concentration at the time of dyeing, excellent stability against alkali when cold pad dyeing, excellent leveling and fastness of all, less pollution to other fibers, It has excellent build-up properties.

` ----- [Ⅰ]` ----- [Ⅰ]

----- [Ⅱ] ----- [Ⅱ]

----- [Ⅲ] ----- [Ⅲ]

상기 식들에서, A는 다음 일반식[A-1] 또는 [A-2]로 표시되는 벤젠 또는 나프탈렌계 아민 화합물이고, R1, R2, R3는 수소, 메틸기, 에틸기, 메톡시기, 에톡시기, 카르복실기, 히드록실기 또는 설폰기이고, R4, R5는 수소, 메틸기, 에틸기, 메톡시기, 에톡시기, 히드록실기 또는 클로로기이고 X는 -CH2CH2OSO3H, -CH 2CH2SSO3H 또는 -CH2=CH2 이고 n은 0∼2인 정수이다.In the above formulas, A is a benzene or naphthalene amine compound represented by the following general formula [A-1] or [A-2], and R 1, R 2 , R 3 are hydrogen, methyl group, ethyl group, methoxy group, ethoxy A time period, a carboxyl group, a hydroxyl group or a sulfone group, R 4 , R 5 are hydrogen, a methyl group, an ethyl group, a methoxy group, an ethoxy group, a hydroxyl group or a chloro group and X is -CH 2 CH 2 OSO 3 H, -CH 2 CH 2 SSO 3 H or —CH 2 = CH 2 and n is an integer from 0 to 2 .

----- [A-1] ----- [A-1]

----- [A-2] ----- [A-2]

본 발명에서 심도있는 청색이라는 것은 청색염료를 사용하여 정해진 농도에 따라 섬유를 청색으로 염색하였을 때 염색물의 염색강도(Dyeing power : 이하 D.P라 한다)가 몰 흡광계수에 비하여 높은 것을 말하며, 빌드업성이 우수하다는 것은 염착성이 좋아 현색성(顯色性)을 장시간 유지하는 성질이 우수하다는 것을 의미한다.In the present invention, the deep blue means that the dyeing power (Dyeing power: hereinafter referred to as DP) of the dye when the fiber is dyed blue according to a predetermined concentration using a blue dye is higher than the molar extinction coefficient. Excellent means good dyeing property and excellent property of maintaining color development for a long time.

종래 셀룰로오즈, 셀룰로오즈/나일론 등과 같은 직물을 청색으로 염색하는데 사용되는 반응성 청색염료로서 대표적인 것들은 대한민국 특허등록 1987-0000218호에서 소개되는 다음 구조식[Ⅳ]의 청색염료와 대한민국 특허등록 1991-0006718호의 실시예 7과 12에서 소개되는 각각 위 구조식[Ⅱ]와 구조식[Ⅲ]으로 표시될 수 있는 다음 구조식[Ⅴ]와 구조식[Ⅵ]의 청색염료가 있다.Reactive blue dyes conventionally used for dyeing fabrics such as cellulose, cellulose / nylon, etc. in blue are representative of the blue dye of the following structural formula [IV] and Korea Patent Registration 1991-0006718, which are introduced in Korean Patent Registration No. 1987-0000218. There are blue dyes of the following structural formulas [V] and [VI] which can be represented by the above structural formulas [II] and [III] respectively, which are introduced in 7 and 12, respectively.

----- [Ⅳ]                                                         ----- [Ⅳ]

----- [Ⅴ]                                                     ----- [Ⅴ]

----- [Ⅵ]                                                   ----- [Ⅵ]

상기 구조식[Ⅴ]와 [Ⅵ]으로 표시되는 청색염료의 경우 빌드업성이 떨어져 진한 색상이 나오지 않는 문제가 있다. 빌드업성 특성은 경제적인 관점에서 뿐만아니라 진하게 착색된 제품을 선호하는 최근의 경향 때문에 중요한 것이며, 따라서 현재 개선의 노력이 이루어지고 있다. 그래서 그동안 많은 연구자들이 심도있는 청색을 보이는 진한 반응성 청색염료를 얻기 위해 많은 노력을 하였음에도 불구하고, 다양한 물성을 만족시킬 수 있는 염료로서는 아직 미흡한 실정에 있다. 예를 들어 상기 구조식[Ⅴ]와 [Ⅵ]으로 표시되는 화합물의 경우에서처럼 심도있는 청색이 나오지 않거나, 상기 구조식[Ⅳ]로 표시되는 화합물에서처럼 진한 반응성 청색염료를 얻은 경우에도 균염성, 발염성 그리고 오염성, 제반견뢰도등에서 불만스러운 경우가 많았다. 여기서 타섬유에 대한 오염성이란 면/나일론 혼방 섬유를 반응성 염료로 염색할 때 반응성 염료는 면에만 염색이 되어야 하는데 나일론에도 약하게 염색되는 것을 말한다.In the case of the blue dyes represented by the structural formulas [V] and [VI], there is a problem that a dark color does not come out due to poor buildup properties. Build-up characteristics are important not only from an economic point of view, but also because of the recent trend to favor darkly colored products, and improvements are currently being made. So many researchers have tried to obtain a deep reactive blue dye showing a deep blue color, but it is still insufficient as a dye that can satisfy a variety of properties. For example, even when the deep blue color does not come out as in the case of the compounds represented by the structural formulas [V] and [VI], or when the dark reactive blue dye is obtained as in the compound represented by the structural formula [IV], Many people were unsatisfied with the pollutants and overall fastness. Contamination to other fibers here means that when dyeing cotton / nylon blended fibers with reactive dyes, the reactive dyes should be dyed only on cotton, but are also weakly dyed on nylon.

따라서 뛰어난 알칼리 안정성으로 콜드패드 염색이 가능하고, 타섬유에 대한 오염성과 제반견뢰도, 균염성이 좋으면서 동시에 염색시 심도있는 청색을 나타내어 적은양으로 높은 D.P를 보이는 환경친화적인 염료의 개발이 요망되는 실정에 있다.Therefore, it is possible to dye cold pads with excellent alkali stability, and it is desirable to develop environmentally friendly dyes that show high levels of DP with small amount of contaminants, good color fastness and good leveling of other fibers and deep blue color at the same time. There is a situation.

본 발명의 목적은 셀룰로오즈, 셀룰로오즈/나일론 등의 직물을 청색으로 염색시 매우 심도있는 청색을 나타내며, 염욕내에 존재하는 알칼리 성분에 대한 안정성이 뛰어나 콜드패드 염색이 가능하고, 제반 견뢰도와 균염성이 뛰어나고, 염색시 셀룰로오즈 이외의 타섬유에 대한 오염성이 적어 원하는 색상을 얻을 수 있으며 수세시 물소비가 적어 폐수량을 감소시킬 수 있는 반응성 청색염료 조성물을 제공하는데 있다.An object of the present invention is very deep blue when dyeing fabrics such as cellulose, cellulose / nylon, and blue, excellent stability to the alkali components present in the salt bath, cold pad dyeing, excellent fastness and uniformity In order to provide a reactive blue dye composition that can reduce the amount of waste water due to less water consumption when washing, since it is less contaminated to other fibers other than cellulose during dyeing.

본 발명자들은 매우 밝은 색상으로 타섬유에 대한 우수한 오염성과 제반견뢰도를 보이는 일반식[Ⅱ]와 [Ⅲ]로 표시되는 염료에 흑색염료를 조성할 때 이용되는 구조식[Ⅰ]로 표시되는 염료(C.I Reactive Black 5등과 같은)를 일정량 함유시켜 염료조성물을 형성시켜 주게되면 염색시 심도있는 청색을 나타내면서 제반견뢰도가 좋고 타섬유에 대한 오염성이 낮은 청색염료 조성물을 얻을 수 있는 것을 확인하여 본 발명을 완성하게 되었다. The inventors have found that the dye represented by the structural formula [I], which is used to form a black dye in the dyes represented by general formulas [II] and [III], which shows excellent staining and overall fastness to other fibers in very bright colors. When a dye composition is formed by containing a certain amount of Reactive Black 5, etc.), the present invention is completed by confirming that a blue dye composition exhibiting a deep blue color at the time of dyeing and having good fastness and low pollution to other fibers can be obtained. It became.

본 발명은 다음 일반식[I]로 표시되는 화합물 30∼80 중량%와 다음 일반식[Ⅱ]로 표시되는 화합물 10∼50 중량% 및 다음 일반식[Ⅲ]으로 표시되는 화합물 10∼50 중량%를 혼합하여서 조성된 반응성 청색염료 조성물에 관한 것이다.The present invention provides 30 to 80% by weight of the compound represented by the following general formula [I], 10 to 50% by weight of the compound represented by the following general formula [II] and 10 to 50% by weight of the compound represented by the following general formula [III] It relates to a reactive blue dye composition formed by mixing.

` ----- [Ⅰ]` ----- [Ⅰ]

----- [Ⅱ] ----- [Ⅱ]

----- [Ⅲ] ----- [Ⅲ]

상기 식들에서, A는 다음 일반식[A-1] 또는 [A-2]로 표시되는 벤젠 또는 나프탈렌계 아민 화합물이고, R1, R2, R3는 수소, 메틸기, 에틸기, 메톡시기, 에톡시기, 카르복실기, 히드록실기 또는 설폰기이고, R4, R5는 수소, 메틸기, 에틸기, 메톡시기, 에톡시기, 히드록실기 또는 클로로기이고 X는 -CH2CH2OSO3H, -CH 2CH2SSO3H 또는 -CH2=CH2 이고 n은 0∼2인 정수이다.In the above formulas, A is a benzene or naphthalene amine compound represented by the following general formula [A-1] or [A-2], and R 1, R 2 , R 3 are hydrogen, methyl group, ethyl group, methoxy group, ethoxy A time period, a carboxyl group, a hydroxyl group or a sulfone group, R 4 , R 5 are hydrogen, a methyl group, an ethyl group, a methoxy group, an ethoxy group, a hydroxyl group or a chloro group and X is -CH 2 CH 2 OSO 3 H, -CH 2 CH 2 SSO 3 H or —CH 2 = CH 2 and n is an integer from 0 to 2 .

----- [A-1] ----- [A-1]

----- [A-2] ----- [A-2]

본 발명의 조성물에 사용된 일반식[Ⅰ]의 염료는 흑색염료를 조성할 때 사용되는 염료로써 흑색에 가까운 청색을 보여 심도있는 색상을 제공하는 것이 특징이며, 우수한 용해도와 균염성를 보여 액상염료의 제조가 용이하다.The dye of the general formula [I] used in the composition of the present invention is a dye used when forming a black dye, and is characterized by providing a deep color by showing a blue color close to black, and showing excellent solubility and homogenization. Easy to manufacture

한편 일반식[Ⅱ]와 [Ⅲ]의 청색 염료는 일반식[Ⅰ]의 염료만으로는 우수한 오염성과 제반견뢰도를 얻지 못하는 것을 보완해 높은 심도와 동시에 오염성과 제반견뢰도에 효과가 있는 청색염료를 제공할 수 있다.On the other hand, the blue dyes of formulas [II] and [III] compensate for the inability to obtain excellent contamination and overall fastness only with the dyes of general formula [Ⅰ] to provide blue dyes effective in high depth and at the same time. Can be.

일반식[I], 일반식[Ⅱ]와 일반식[Ⅲ]의 혼합물을 상기한 비율로 조정하여 제조한 반응성 청색염료 조성물은 침염, 날염 및 콜드패드 염색시 매우 심도있는 청색을 나타내고, 알칼리에 대한 안정성이 우수하고, 균염성과 제반견뢰도가 뛰어나며, 타섬유에 대한 오염성이 적었음을 알 수 있었다.The reactive blue dye composition prepared by adjusting the mixture of general formula [I], general formula [II] and general formula [III] in the above-mentioned ratio shows very deep blue color in dyeing, printing and cold pad dyeing. It was found to be excellent in stability, good leveling and fastness, and low contamination to other fibers.

이하 실시예를 들어 본 발명을 구체적으로 설명한다.The present invention will be described in detail with reference to the following Examples.

<실시예 1><Example 1>

일반식[Ⅰ]로 표시될 수 있는 다음 구조식[Ⅶ]의 염료화합물 31중량부와31 parts by weight of the dye compound of the following structural formula [VII] which can be represented by the general formula [I]

----- [Ⅶ] ----- [Ⅶ]

일반식[Ⅱ]로 표시될 수 있는 다음 구조식[Ⅷ]의 염료화합물 39중량부와39 parts by weight of a dye compound represented by the following formula [VII] which can be represented by the general formula [II]

----- [Ⅷ]                                                  ----- [Ⅷ]

일반식[Ⅲ]으로 표시될 수 있는 다음 구조식[Ⅸ]의 염료화합물 30중량부를 혼합하여 염료조성물을 제조하였다.A dye composition was prepared by mixing 30 parts by weight of the dye compound of the following structural formula [VII], which may be represented by the general formula [III].

-----[Ⅸ] ----- [Ⅸ]

이렇게 제조된 염료 조성물을 면 염색시 나일론을 넣고 염색을 한다. 염색이 종료되면 면과 나일론을 수세한 후 나일론은 건조하고 면은 쇼핑후 건조한다. 건조된 나일론의 오염된 정도를 확인하였다.The dye composition thus prepared is dyed with nylon in cotton dyeing. After dyeing, wash the cotton and nylon, and then the nylon is dried and the cotton is dried after shopping. The degree of contamination of the dried nylon was checked.

본 <실시예 1>에서 얻어진 건조된 면과 다음 <표 1>에 기재된 종래의 청색염료 화합물들을 사용하여 얻어진 면의 염색강도와 오염도를 측정하고 그 결과를 다음 <표 1>에 나타냈다. 종래의 염료화합물을 기준으로 본 실시예 염료조성물의 D.P는 160%이상 우수하였으며, 나일론에 대한 세탁견뢰도는 다음 <표 1>에 기재된 종래의 염료 화합물은 4급이었으나 본 실시예의 염료조성물은 5급으로 우수하였다.Dyeing strength and staining degree of the cotton obtained using the dried cotton obtained in this <Example 1> and the conventional blue dye compounds described in the following <Table 1> were measured, and the results are shown in the following <Table 1>. DP of this example dye composition was superior to more than 160% based on the conventional dye compound, and the fastness to washability for nylon was the fourth dye compound shown in the following <Table 1>, but the dye composition of this example was grade 5 Was excellent.

< 표 1 ><Table 1>

실시예1의 염료조성물 Dye Composition of Example 1 종래 염료화합물 Conventional dye compound D.P D.P 오염도 Pollution 반응성 적색염료 Reactive Red Dye D.P D.P 오염도 Pollution 165% 165% 5급 Grade 5 구조식[Ⅴ]의 화합물 Compound of Structural Formula [V] 100% 100% 4급 Grade 4 160% 160% 구조식[Ⅵ]의 화합물 Compound of Structural Formula [VI] 4급 Grade 4

<실시예 2><Example 2>

일반식[Ⅰ]로 표시될 수 있는 실시예 1에서의 구조식[Ⅶ]의 염료화합물 26중량부와 일반식[Ⅱ]로 표시될 수 있는 다음 구조식[Ⅹ]의 염료화합물 36중량부와26 parts by weight of the dye compound of Structural Formula [VII], which may be represented by Formula [I], and 36 parts by weight of the dye compound of the following Structural Formula [VII], which may be represented by Formula [II]

----- [Ⅹ]                                                    ----- [Ⅹ]

일반식[Ⅲ]으로 표시될 수 있는 다음 구조식[ⅩⅠ]의 염료화합물 38중량부를 혼합하여 염료조성물을 제조하였다.A dye composition was prepared by mixing 38 parts by weight of the dye compound of the following structural formula [VII], which may be represented by the general formula [III].

----- [ⅩⅠ]----- [ⅩⅠ]

이렇게 제조된 염료 조성물을 면 염색시 나일론을 넣고 염색을 한다. 염색이 종료되면 면과 나일론을 수세한 후 나일론은 건조하고 면은 쇼핑후 건조한다. 건조된 나일론의 오염된 정도를 확인하였다. The dye composition thus prepared is dyed with nylon in cotton dyeing. After dyeing, wash the cotton and nylon, and then the nylon is dried and the cotton is dried after shopping. The degree of contamination of the dried nylon was checked.

본 <실시예 2>에서 얻어진 건조된 면과 다음 <표 2>에 기재된 종래의 청색 염료 화합물을 사용하여 얻어진 면의 염색강도와 오염도를 측정하고 그 결과를 다음 <표 2>에 나타냈다. 종래의 염료화합물을 기준으로 본 실시예 염료조성물의 D.P는 161%이상 우수하였으며, 나일론에 대한 세탁견뢰도는 다음 <표 2>에 기재된 종래의 염료 화합물들은 4급이었으나 본 실시예의 염료조성물은 5급으로 우수하였다.Dyeing intensity and staining degree of the cotton obtained using the dried cotton obtained in this <Example 2> and the conventional blue dye compound of following <Table 2> were measured, and the result is shown in following <Table 2>. DP of this example dye composition was superior to 161% based on the conventional dye compound, and the laundry fastness to nylon was grade 4 of the conventional dye compounds shown in <Table 2>, but the dye composition of this example was grade 5 Was excellent.

<표 2>TABLE 2

실시예2의 염료조성물 Dye composition of Example 2 종래 염료화합물 Conventional dye compound D.P D.P 오염도 Pollution 반응성 적색염료 Reactive Red Dye D.P D.P 오염도 Pollution 163% 163% 5급 Grade 5 구조식[Ⅴ]의 화합물 Compound of Structural Formula [V] 100% 100% 4급 Grade 4 161% 161% 구조식[Ⅵ]의 화합물 Compound of Structural Formula [VI] 4급 Grade 4

<실시예 3><Example 3>

일반식[Ⅰ]로 표시될 수 있는 실시예 1에서의 구조식[Ⅶ]의 염료화합물 29중량부와 일반식[Ⅱ]로 표시될 수 있는 실시예 2에서의 구조식[Ⅹ]의 염료화합물 41중량부와 일반식[Ⅲ]으로 표시될 수 있는 다음 구조식[ⅩⅡ]의 염료화합물 30중량부를 혼합하여 염료조성물을 제조하였다.29 parts by weight of the dye compound of Structural Formula [VII], which can be represented by General Formula [I], and 41 weight of the dye compound of Structural Formula [VIII], which can be represented by General Formula [II] A dye composition was prepared by mixing 30 parts by weight of the dye compound with the following structural formula [XII], which can be represented by the following formula and [III].

----- [ⅩⅡ]----- [XII]

이렇게 제조된 염료 조성물을 면 염색시 나일론을 넣고 염색을 한다. 염색이 종료되면 면과 나일론을 수세한 후 나일론은 건조하고 면은 쇼핑후 건조한다. 건조된 나일론의 오염된 정도를 확인하였다.The dye composition thus prepared is dyed with nylon in cotton dyeing. After dyeing, wash the cotton and nylon, and then the nylon is dried and the cotton is dried after shopping. The degree of contamination of the dried nylon was checked.

본 실시예 3에서 얻어진 건조된 면과 다음 <표 3>에 기재된 종래의 청색 염료 화합물을 사용하여 얻어진 면의 염색강도와 오염도를 측정하고 그 결과를 다음 <표 3>에 나타냈다. 종래의 염료화합물을 기준으로 본 실시예 염료조성물의 D.P는 167%이상 우수하였으며, 나일론에 대한 세탁견뢰도는 다음 <표 3>에 기재된 종래의 염료 화합물들은 4급이었으나 본 실시예의 염료조성물은 5급으로 우수하였다.Dyeing strength and staining degree of the dried cotton obtained in Example 3 and the cotton obtained using the conventional blue dye compound described in Table 3 below were measured, and the results are shown in Table 3 below. DP of this example dye composition was superior to 167% based on the conventional dye compound, and the laundry fastness to nylon was grade 4 of the conventional dye compounds shown in <Table 3>, but the dye composition of the present example was grade 5 Was excellent.

<표 3>TABLE 3

실시예3의 염료조성물 Dye composition of Example 3 종래 염료화합물 Conventional dye compound D.P D.P 오염도 Pollution 반응성 적색염료 Reactive Red Dye D.P D.P 오염도 Pollution 163% 163% 5급 Grade 5 구조식[Ⅴ]의 화합물 Compound of Structural Formula [V] 100% 100% 4급 Grade 4 167% 167% 구조식[Ⅵ]의 화합물 Compound of Structural Formula [VI] 4급 Grade 4

상기 실시예들에서 제조된 본 발명의 청색염료 조성물은 용해성이 우수하여 액체 조성물로도 제조가 가능하여 분진이 없으며, 용해과정이 생략되어 현장 자동 염색기에도 사용 가능하여 현장 작업자의 작업환경을 개선시킬 수 있는 장점이 있다.The blue dye composition of the present invention prepared in the above embodiments is excellent in solubility and can be prepared as a liquid composition, there is no dust, and the dissolution process is omitted, so that it can be used in an on-site automatic dyeing machine to improve the working environment of the field worker. There are advantages to it.

본 발명의 염료조성물은 셀룰로오즈, 셀룰로오즈/나일론 등의 직물을 청색으로 염색시 매우 심도있는 청색을 나타내며, 염욕내에 존재하는 알칼리 성분에 대한 안정성이 뛰어나 콜드패드 염색이 가능하고, 제반 견뢰도와 균염성이 뛰어나며, 염색시 셀룰로오즈 이외의 타섬유에 대한 오염성이 적어 원하는 색상을 얻을 수 있으며 수세시 물소비가 적어 폐수량을 감소시킬 수 있는 효과를 갖는다.The dye composition of the present invention exhibits very deep blue color when dyed fabrics such as cellulose, cellulose / nylon, etc., and has excellent stability to alkali components present in the salt bath, which enables cold pad dyeing, and has good fastness and leveling properties. Excellent dyeing, less staining of other fibers other than cellulose can be obtained the desired color and water consumption when washed with water has the effect of reducing the waste water.

Claims (1)

다음 일반식[I]로 표시되는 화합물 30∼80 중량%와 다음 일반식[Ⅱ]로 표시되는 화합물 10∼50 중량% 및 다음 일반식[Ⅲ]으로 표시되는 화합물 10∼50 중량%를 혼합하여서 조성된 반응성 청색염료 조성물.30 to 80% by weight of the compound represented by the following general formula [I], 10 to 50% by weight of the compound represented by the following general formula [II] and 10 to 50% by weight of the compound represented by the following general formula [III] Formulated reactive blue dye composition. ` ----- [Ⅰ]` ----- [Ⅰ] ----- [Ⅱ] ----- [Ⅱ] ----- [Ⅲ] ----- [Ⅲ] 상기 식들에서, A는 다음 일반식[A-1] 또는 [A-2]로 표시되는 벤젠 또는 나프탈렌계 아민 화합물이고, R1, R2, R3는 수소, 메틸기, 에틸기, 메톡시기, 에톡시기, 카르복실기, 히드록실기 또는 설폰기이고, R4, R5는 수소, 메틸기, 에틸기, 메톡시기, 에톡시기, 히드록실기 또는 클로로기이고 X는 -CH2CH2OSO3H, -CH 2CH2SSO3H 또는 -CH2=CH2 이고 n은 0∼2인 정수이다.In the above formulas, A is a benzene or naphthalene amine compound represented by the following general formula [A-1] or [A-2], and R 1, R 2 , R 3 are hydrogen, methyl group, ethyl group, methoxy group, ethoxy A time period, a carboxyl group, a hydroxyl group or a sulfone group, R 4 , R 5 are hydrogen, a methyl group, an ethyl group, a methoxy group, an ethoxy group, a hydroxyl group or a chloro group and X is -CH 2 CH 2 OSO 3 H, -CH 2 CH 2 SSO 3 H or —CH 2 = CH 2 and n is an integer from 0 to 2 . ----- [A-1] ----- [A-1] ----- [A-2] ----- [A-2]
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