JPH07258571A - Red disperse dye composition and method of dyeing hydrophobic fibrous material therewith - Google Patents

Red disperse dye composition and method of dyeing hydrophobic fibrous material therewith

Info

Publication number
JPH07258571A
JPH07258571A JP6208274A JP20827494A JPH07258571A JP H07258571 A JPH07258571 A JP H07258571A JP 6208274 A JP6208274 A JP 6208274A JP 20827494 A JP20827494 A JP 20827494A JP H07258571 A JPH07258571 A JP H07258571A
Authority
JP
Japan
Prior art keywords
dye
formula
parts
dye composition
dyeing
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP6208274A
Other languages
Japanese (ja)
Other versions
JP3310471B2 (en
Inventor
Yoshiyuki Sato
善之 佐藤
Yoshiki Akatani
宜樹 赤谷
Yasuo Murakami
靖夫 村上
Kazumasa Yoshioka
和真 吉岡
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Kayaku Co Ltd
Original Assignee
Nippon Kayaku Co Ltd
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 JP6-32010 external-priority
Application filed by Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd
Priority to JP20827494A priority Critical patent/JP3310471B2/en
Publication of JPH07258571A publication Critical patent/JPH07258571A/en
Application granted granted Critical
Publication of JP3310471B2 publication Critical patent/JP3310471B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • 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
    • C09B67/0051Mixtures of two or more azo dyes mixture of two or more monoazo dyes

Abstract

PURPOSE:To dye a material composed of fibers of different finenesses to produce a dyed piece excellent in level dyeing and fastness. CONSTITUTION:The composition comprises a dye represented by formula I, a dye represented by formula II (wherein R is hydrogen or lower alkyl) and optionally a dye represented by formula III and/or a dye represented by formula IV.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、染料組成物およびそれ
を用いる染色法に関する。更に詳しくは、特定の染料を
配合した水不溶性の分散染料組成物およびそれを用いる
疎水性繊維の染色法に関する。
FIELD OF THE INVENTION The present invention relates to a dye composition and a dyeing method using the same. More specifically, it relates to a water-insoluble disperse dye composition containing a specific dye and a method for dyeing a hydrophobic fiber using the same.

【0002】[0002]

【従来の技術】近年、各繊維メーカーより合繊の持つ特
徴を生かした差別化商品が新合繊として生み出されてい
る。これらの差別化商品を構成する原糸は、極細繊維、
特殊断面糸、異収縮混繊糸などそれぞれに特性を持った
差別化繊維の複合加工または組合わせにより構成されて
おり、シルクライク素材、薄起毛織編物(ピーチスキ
ン)、レーヨンライク素材など天然繊維にはない合繊特
有の質感、風合いが受入れられたこともあり急速に市場
に拡大している。
2. Description of the Related Art In recent years, differentiated products that utilize the characteristics of synthetic fibers have been created as new synthetic fibers by various fiber manufacturers. The yarns that make up these differentiated products are ultrafine fibers,
Composed of a composite processing or combination of differentiated fibers with special characteristics such as special cross-section yarns and different shrinkage mixed yarns. Natural fibers such as silk-like material, thin napped knitted fabric (peach skin), rayon-like material The texture and texture peculiar to synthetic fibers, which is not available in the market, has been accepted, and is rapidly expanding into the market.

【0003】しかし、これらの新感性の素材の染色加工
にあたっては、特に繊維が極細化され、繊維の表面積が
増大したことに起因する問題があり、具体的には (1)繊維表面での反射光が増して、染色物の視感濃度
が低下する。 (2)光による酸化・還元を受け易く、耐光堅牢度が低
下する。 (3)(1)のために、単位面積当りの染料使用量が増
大し、その結果、染色物の昇華および湿潤堅牢度が低下
する。 (4)複合化された繊維の太さが異なることによる染色
物のイラツキ(不均染)が生じる。 などの問題である。
However, there is a problem in dyeing and processing these new-sensitized materials, especially because the fibers are extremely fine and the surface area of the fibers is increased. Specifically, (1) reflection on the fiber surface The increase in light reduces the visual density of the dyed product. (2) It is susceptible to oxidation / reduction by light, and the light fastness is lowered. (3) Due to (1), the amount of dye used per unit area increases, and as a result, the dye sublimation and wet fastness decrease. (4) Irregularity (disproportionate dyeing) occurs in the dyed product due to the different thickness of the composited fibers. It is a problem such as.

【0004】[0004]

【発明が解決しようとする課題】これらの問題点を解決
するためには、ビルドアップ性に優れ、かつ高堅牢性を
有した染料を使用する必要があるだけでなく、異なる太
さの糸が複合された素材の均染性あるいは同色性に優れ
た染料を使用する必要がある。しかし、現在市場で用い
られている製品でこれらの性質を十分に兼ね備えている
ものは少ない。したがって、これらの性質を十分に兼ね
備えた染料の開発が望まれている。
In order to solve these problems, it is necessary not only to use a dye having excellent build-up property and high fastness, but also to use yarns having different thicknesses. It is necessary to use a dye that is excellent in levelness or color uniformity of the composite material. However, few products currently used in the market have these properties sufficiently. Therefore, development of a dye sufficiently having these properties is desired.

【0005】[0005]

【課題を解決するための手段】本発明者らは前記したよ
うな課題を解決すべく誠意研究を重ねた結果、特定の構
造で示される分散染料を配合して染色を行なうことによ
り前記課題が解決されることを見出し、本発明を完成さ
せたものである。即ち本発明は(1)式(1)
Means for Solving the Problems The present inventors have conducted sincerity research to solve the above-mentioned problems, and as a result, the above-mentioned problems were solved by blending a disperse dye having a specific structure and dyeing. The inventors have completed the present invention by finding out that they will be solved. That is, the present invention relates to the formula (1) (1)

【0006】[0006]

【化5】 [Chemical 5]

【0007】で示される染料、式(2)The dye represented by the formula (2)

【0008】[0008]

【化6】 [Chemical 6]

【0009】(式(2)中、Rは水素または低級アルキ
ル基を示す。)で示される染料および必要により式
(3)
(In the formula (2), R represents hydrogen or a lower alkyl group) and optionally the formula (3)

【0010】[0010]

【化7】 [Chemical 7]

【0011】で示される染料および/または式(4)The dye represented by and / or the formula (4)

【0012】[0012]

【化8】 [Chemical 8]

【0013】で示される染料を含有してなることを特徴
とする赤色分散染料組成物及びこれを用いることを特徴
とする疎水性繊維材料の染色法を提供する。なお本発明
において「低級アルキル」とは炭素数1乃至4のアルキ
ルを意味する。
There is provided a red disperse dye composition comprising a dye represented by: and a method for dyeing a hydrophobic fiber material characterized by using the red disperse dye composition. In the present invention, the "lower alkyl" means alkyl having 1 to 4 carbon atoms.

【0014】本発明を詳細に説明する。一般に、アゾ系
分散染料はビルドアップ性に優れ、かつ比較的高堅牢性
を兼ね備えた染料が多いが、均染性が劣る。またアンス
ラキノン系分散染料は耐光堅牢度、均染性に優れたもの
が多いが、ビルドアップ性、昇華堅牢度等が劣るといっ
た傾向にある。したがって、淡色〜中色分野にはアンス
ラキノン系染料が、中色〜濃色分野にはアゾ系染料が主
に使用されてきた。しかし、前述の如く、繊維の極細化
および複合化された素材の染色に当たっては従来のよう
な染料の使い分けでは対応し難くなってきた。特に、異
繊度糸の複合素材のの染色においては、極細糸側とレギ
ュラー糸側の染着量が同じであっても、前述の如き理由
で極細糸側の視感濃度が低下ことによる染色物のイラツ
キ(不均染)が生じるという問題がある。したがって、
このような素材を均一あるいは同色に染色し得る性質が
必要とされる。またそれと同時に極細糸側では、前述の
如く従来よりより高い堅牢度水準が要求される。
The present invention will be described in detail. Generally, many azo disperse dyes are excellent in build-up property and have relatively high fastness, but they are inferior in level dyeing property. Many of the anthraquinone disperse dyes are excellent in light fastness and level dyeability, but tend to be inferior in build-up properties, sublimation fastness, and the like. Therefore, anthraquinone dyes have been mainly used in the light to medium color fields, and azo dyes have been mainly used in the medium to dark color fields. However, as described above, it has become difficult to dye fibers made of fine fibers and composite materials by using conventional dyes properly. In particular, in the dyeing of a composite material of different fineness yarns, even if the amount of dyeing on the ultrafine yarn side and the regular yarn side are the same, the dyed product resulting from a decrease in the luminous density of the ultrafine yarn side for the reasons described above. There is a problem that unevenness (uneven dyeing) occurs. Therefore,
It is necessary to have the property of being able to dye such a material uniformly or in the same color. At the same time, the ultrafine yarn side is required to have a higher level of fastness than ever before, as described above.

【0015】本発明者らは式(1)および式(2)され
には必要により式(3)および/または式(4)で示さ
れる染料を配合して用いることにより異繊度糸の複合素
材の均染性に優れ、かつ高堅牢性を有する染料組成物が
得られることを見い出し、本発明に達した。すなわち、
本発明の染料組成物を用いて、前述のような複合素材を
染色すれば均染性に優れ、かつ堅牢度の良好な染色物が
得られるものである。
The inventors of the present invention use the dyes represented by the formula (3) and / or the formula (4) if necessary in addition to the formulas (1) and (2), and use the composite material of the different fineness yarn. It has been found that a dye composition having excellent level dyeability and high fastness can be obtained, and the present invention has been accomplished. That is,
By dyeing the above-mentioned composite material with the dye composition of the present invention, a dyed product having excellent levelness and fastness can be obtained.

【0016】本発明の染料組成物は、好ましくは式
(1)で示される染料を20〜60重量%、式(2)で
示される染料を20〜50重量%さらに必要により式
(3)で示される染料を好ましくは0〜40重量%式
(4)で示される染料をは好ましくは0〜20重量%割
合で配合して調製される。さらに特に好ましくは、式
(1)で示される染料を30〜40重量%、式(2)で
示される染料を30〜40重量%、式(3)で示される
染料を20〜30重量%および式(4)で示される染料
を5〜15重量%の割合で配合して調製される。式
(3)および式(4)で示される染料はいずれも色相あ
るいは堅牢度等目的に応じて添加することができ、これ
らの染料が無添加であっても本発明の目的は達成される
ものである。
The dye composition of the present invention preferably contains 20 to 60% by weight of the dye represented by the formula (1), 20 to 50% by weight of the dye represented by the formula (2), and optionally the compound represented by the formula (3). The dye represented by the formula (4) is preferably prepared by blending the dye represented by the formula (4) in an amount of 0 to 20% by weight. More preferably, the dye represented by formula (1) is 30 to 40% by weight, the dye represented by formula (2) is 30 to 40% by weight, the dye represented by formula (3) is 20 to 30% by weight, and It is prepared by blending the dye represented by the formula (4) at a ratio of 5 to 15% by weight. The dyes represented by the formulas (3) and (4) can be added according to the purpose such as hue or fastness, and the object of the present invention can be achieved even if these dyes are not added. Is.

【0017】本発明で用いられる式(2)の染料の具体
的な例としては例えば、
Specific examples of the dye of the formula (2) used in the present invention include:

【0018】[0018]

【化9】 [Chemical 9]

【0019】[0019]

【化10】 [Chemical 10]

【0020】等が挙げられ、これらの混合物も使用でき
る。
And the like, and a mixture thereof can also be used.

【0021】次に本発明の染料組成物を調製するに当た
って使用される式(1)で示される染料は特公昭59−
39471号によって、式(2)で示される染料は特公
昭44−13389号、特公昭44−20269号によ
って、式(3)で示される染料は特公昭44−3062
8号、特公昭45−8750号によって、式(4)で示
される染料は特公昭43−4212号、特公昭43−1
5310号によってそれぞれ公知であり、それらに記載
の方法で染料原末を製造できる。
Next, the dye represented by the formula (1) used in preparing the dye composition of the present invention is described in JP-B-59-
No. 39471, the dye represented by the formula (2) is described in JP-B-44-13389 and JP-B-44-20269, and the dye represented by the formula (3) is disclosed in JP-B-44-3062.
8 and JP-B-45-8750, the dye represented by the formula (4) is represented by JP-B-43-4212 and JP-B-43-1.
No. 5310 is known, and dye bulk powders can be produced by the methods described therein.

【0022】本発明の染料組成物は式(1)、式(2)
および必要により式(3)および/または式(4)で示
される染料の各原末を前記したような配合比で混合した
後、微粒子化(分散化)処理を施して染料組成物として
もよいし、また、これらの染料原末について別々に微粒
子化(分散化)処理を施した後、前記したような割合に
混合してもよい。後者にあっては染浴に個々に微粒子化
(分散化)された染料を添加し、本発明の染料組成物と
同じ組成を染浴中で形成させてもよい。
The dye composition of the present invention comprises formulas (1) and (2).
And, if necessary, the respective bulk powders of the dyes represented by the formula (3) and / or the formula (4) are mixed in the above-described mixing ratio, and then finely divided (dispersed) to give a dye composition. Alternatively, the raw powders of these dyes may be separately made into fine particles (dispersion) and then mixed in the proportions as described above. In the latter case, the finely divided (dispersed) dyes may be added to the dye bath to form the same composition as the dye composition of the present invention in the dye bath.

【0023】式(1)、式(2)、式(3)および式
(4)で示される染料の原末またはそれらの混合物を微
粒子化処理するに当たっては、一般的には染料の原末を
ナフタレンスルホン酸とアルキルベンゼンスルホン酸の
ホルマリン縮合物、ナフタレンスルホン酸のホルマリン
縮合物、クレゾールスルホン酸のホルマリン縮合物、ク
レゾールと2−ナフトール−6スルホン酸のホルマリン
縮合物、アルキルナフタレンスルホン酸のホルマリン縮
合物、クレオソート油スルホン酸のホルマリン縮合物、
リグニンスルホン酸等のアニオン分散剤、またはエチレ
ンオキサイドとプロピレンオキサイドとのブロック共重
合物、アルキルフェノールのエチレンオキサイド付加
物、ポリスチレン化フェノールのエチレンオキサイド付
加物等の非イオン分散剤、またはこれらのアニオン分散
剤と非イオン分散剤との混合物と、少量の水の存在下に
ボールミル、サンドグラインダーあるいはサンドミル等
の粉砕機を用いて十分に湿式粉砕することにより行なわ
れる。また、このとき染料原末は通常染料組成物の全量
に対し10〜50重量%の割合で配合される本発明の染
料組成物は微粒子化されたままのペースト状のままで、
あるいは乾燥してから染色に供される。本発明の方法に
より染色し得る疎水性繊維の具体例としてはポリエステ
ル繊維、トリアセテート繊維、ジアセテート繊維、ポリ
アミド繊維およびこれら同志の混紡品があげられ、これ
らとレーヨン等の再生繊維あるいは木綿、絹、羊毛等の
天然繊維との混紡品であってもよい。
When the bulk powder of the dye represented by the formula (1), the formula (2), the formula (3) and the formula (4) or a mixture thereof is subjected to fine particle treatment, the bulk powder of the dye is generally used. Formalin condensate of naphthalene sulfonic acid and alkylbenzene sulfonic acid, formalin condensate of naphthalene sulfonic acid, formalin condensate of cresol sulfonic acid, formalin condensate of cresol and 2-naphthol-6 sulfonic acid, formalin condensate of alkylnaphthalene sulfonic acid , Formalin condensate of creosote oil sulfonic acid,
Anionic dispersants such as lignin sulfonic acid, block copolymers of ethylene oxide and propylene oxide, nonionic dispersants such as alkylphenol ethylene oxide adducts, polystyrene oxide phenol ethylene oxide adducts, or these anionic dispersants. And a nonionic dispersant, and in the presence of a small amount of water, sufficient wet pulverization is performed using a pulverizer such as a ball mill, sand grinder or sand mill. Further, at this time, the bulk dye is usually blended in a proportion of 10 to 50% by weight with respect to the total amount of the dye composition, and the dye composition of the present invention remains in the form of a finely divided paste,
Alternatively, it is dried and then dyed. Specific examples of the hydrophobic fiber which can be dyed by the method of the present invention include polyester fiber, triacetate fiber, diacetate fiber, polyamide fiber and a blended product of the same, and recycled fiber such as rayon or cotton, silk, It may be a blended product with a natural fiber such as wool.

【0024】本発明の方法に使用する式(1)、式
(2)および必要により式(3)および/または式
(4)で示される染料を含有する染料組成物を用いて疎
水性繊維を染色するには、繊維を浸漬した水性溶媒中で
加圧下105℃以上、好ましくは110℃〜140℃で
染色するのが有利である。また、o−フェニルフェノー
ルやトリクロロベンゼン等のキャリヤーの存在下に比較
的高温、例えば水の沸騰状態で染色することもできる。
あるいはまた染料分散液を布にパディングし、150〜
230℃、30秒〜1分間の乾熱処理を施すいわゆるサ
ーモゾル方式での染色も可能である。一方本発明の染料
組成物を天然糊剤(例えばローカストビーンガム、グア
ーガム等)、加工糊剤(例えばカルボキシメチルセルロ
ース等の繊維素誘導体、加工ローカストビーンガム
等)、合成糊剤(例えばポリビニルアルコール、ポリビ
ニル酢酸等)等とともに捺染糊を調整し、布に印捺した
後スチーミングまたはサーモゾル処理する捺染法による
染色を行なってもよい。
Hydrophobic fibers are prepared by using a dye composition containing a dye represented by formula (1), formula (2) and optionally formula (3) and / or formula (4) used in the method of the present invention. For dyeing, it is advantageous to dye at a temperature of 105 ° C. or higher, preferably 110 ° C. to 140 ° C. under pressure in an aqueous solvent in which the fibers are immersed. It is also possible to dye in the presence of a carrier such as o-phenylphenol or trichlorobenzene at a relatively high temperature, for example, boiling water.
Alternatively, pad the cloth with the dye dispersion, and
Dyeing by a so-called thermosol method in which dry heat treatment is performed at 230 ° C. for 30 seconds to 1 minute is also possible. On the other hand, the dye composition of the present invention contains a natural sizing agent (eg, locust bean gum, guar gum, etc.), a processed sizing agent (eg, fiber derivative such as carboxymethyl cellulose, processed locust bean gum, etc.), a synthetic sizing agent (eg, polyvinyl alcohol, polyvinyl). It is also possible to prepare a printing paste together with (acetic acid, etc.) and the like, and after printing on a cloth, dyeing by a printing method of steaming or thermosol treatment.

【0025】以下、本発明の効果を表1および表2によ
って説明する。説明中「部」および「%」はそれぞれ
「重量部」、「重量%」である。表1は、2.0デニー
ルのポリエステル加工糸織物(以下レギュラーPETと
称する)と0.14デニールのポリエステル加工糸織物
(以下極細ポリエステルと称する)を同浴染色したとき
の同色性を比較したものである。本発明の実施例の染料
組成物はいずれも比較例の市販染料よりレギュラーポリ
エステルと極細ポリエステルの濃度差が小さく、即ち同
色性が極めて優れていることがわかる。また表2から本
発明の実施例の染料組成物はいずれも極細素材では高い
水準が求められる耐光、昇華、水の各堅牢度が良好であ
ることがわかる。
The effects of the present invention will be described below with reference to Tables 1 and 2. In the description, "part" and "%" are "part by weight" and "% by weight", respectively. Table 1 compares the same color properties of 2.0 denier polyester processed yarn fabric (hereinafter referred to as regular PET) and 0.14 denier polyester processed yarn fabric (hereinafter referred to as ultrafine polyester) when dyed in the same bath. Is. It can be seen that all the dye compositions of the examples of the present invention have a smaller concentration difference between the regular polyester and the ultrafine polyester than the commercially available dyes of the comparative examples, that is, the same color property is extremely excellent. Further, it can be seen from Table 2 that each of the dye compositions of the examples of the present invention is excellent in light fastness, sublimation, and water fastness, which requires a high level for ultrafine materials.

【0026】[0026]

【表1】 [Table 1]

【0027】(注1)実施例1、2、3および4で得ら
れた各染料組成物を2部を含む全量3000部の各染浴
をそれぞれ調製し、2.0デニールのポリエステル加工
糸織物50部と0.14デニールのポリエステル加工糸
織物50部を浸漬し、130℃で60分間染色した後、
還元洗浄、水洗、乾燥した。比較例として市販染料を実
施例1の染料組成物の染布とほぼ同等の視感濃度となる
ように調整して、同様に染色処理した。 (注2)レギュラーPETに対する極細PETの濃度価
値比をCOMSEKIII測色システム(日本化薬(株)
製)を用いて測色し、算出した。数値が100に近い
程、染色物の濃度価値が近く、同色性が良好といえる。 (注3)比較染料として、Disperse Red
60を使用。
(Note 1) A total of 3000 parts of each dye bath containing 2 parts of each of the dye compositions obtained in Examples 1, 2, 3 and 4 was prepared, respectively, and 2.0 denier polyester processed yarn woven fabric was prepared. 50 parts and 50 parts of 0.14 denier polyester processed yarn fabric are dipped and dyed at 130 ° C. for 60 minutes,
It was reduced, washed with water and dried. As a comparative example, a commercially available dye was prepared so that the visual density was almost the same as that of the dye fabric of the dye composition of Example 1, and the dyeing treatment was performed in the same manner. (Note 2) The density-value ratio of ultra-fine PET to regular PET is calculated by the COMSEK III color measurement system (Nippon Kayaku Co., Ltd.
(Manufactured by Mitsui Chemicals, Inc.) The closer the value is to 100, the closer the density value of the dyed product, and the better the color uniformity. (Note 3) As a comparative dye, Disperse Red
Use 60.

【0028】[0028]

【表2】 [Table 2]

【0029】(注4)実施例1、2、3および4で得ら
れた各染料組成物を2部を含む全量3000部の各染浴
をそれぞれ調製し、ポリエステルトロピカル布100部
をそれぞれに浸漬し、130℃で60分間染色した後、
還元洗浄し、水洗、乾燥して得られた染色物を用いて、
堅牢度試験を実施した。比較例の市販染料は実施例1の
染料組成物の染色物と略同等の視感濃度となるように調
整して、同様に染色処理したものを使用した。
(Note 4) A total of 3000 parts of each dye bath containing 2 parts of each of the dye compositions obtained in Examples 1, 2, 3 and 4 was prepared, and 100 parts of polyester tropical cloth was dipped in each. And dyeing at 130 ° C for 60 minutes,
Using the dyed product obtained by reduction washing, water washing, and drying,
A fastness test was performed. The commercially available dye of the comparative example was prepared so that the dye density of the dye composition of Example 1 was substantially the same as that of the dyed product, and the dye was similarly treated.

【0030】(注5)JIS−L0842、カーボンア
ーク灯法、変褪色の程度をJIS変褪色用ブルースケー
ルで判定。 (注6)JIS−L0879B、180℃,30秒、ポ
リエステル白布への汚染の程度をJIS汚染用グレース
ケールで判定 (注7)染布を180℃で30秒間ヒートセットした
後、水試験(JIS−L0846)を実施し、シルク白
布への汚染の程度をJIS汚染用グレスケールで判定し
た。
(Note 5) JIS-L0842, the carbon arc lamp method, and the degree of discoloration are judged by the JIS blue scale for discoloration. (Note 6) JIS-L0879B, 180 ° C., 30 seconds, the degree of contamination on polyester white cloth is judged by JIS contamination gray scale (Note 7) After heat setting the dyed cloth at 180 ° C. for 30 seconds, water test (JIS -L0846) was carried out, and the degree of contamination on the white silk cloth was judged by the JIS contamination gray scale.

【0031】[0031]

【実施例】以下に実施例をあげて本発明を更に具体的に
説明する。実施例中「部」および「%」はそれぞれ「重
量部」および「重量%」である。
EXAMPLES The present invention will be described in more detail with reference to the following examples. In the examples, "parts" and "%" are "parts by weight" and "% by weight", respectively.

【0032】実施例1 式(1)で示される染料原末10部、式(5)で示され
る染料原末12部、式(3)で示される染料原末8部お
よび式(4)で示される染料原末3部をデモールN(花
王(株)製、アニオン分散剤)67部と共にサンドグラ
インダーを用いて微粒子化(分散化)し、本発明の染料
組成物を得た。この染料組成物2部に、pH4.5に調
整された純水を加えて3000部とした染浴を調製し、
ポリエステルトロピカル布100部を浸漬し、130℃
で60分間染色した後、染色物を45%のカセイソーダ
6部、ハイドロサルファイト6部、サンモールRC−7
00(日華化学(株)製、アニオン界面活性剤)3部に
水を加えて全量3000部とした浴で、80℃、10分
間の還元洗浄を施し、水洗、乾燥して、赤色の染色物を
得た。得られた染色物の耐光、昇華、水堅牢度は良好な
水準であった。
Example 1 With 10 parts of the bulk powder of the formula (1), 12 parts of the bulk powder of the formula (5), 8 parts of the bulk powder of the formula (3) and Formula (4). 3 parts of the dye bulk powder shown were finely divided (dispersed) together with 67 parts of Demol N (manufactured by Kao Corporation, anion dispersant) using a sand grinder to obtain a dye composition of the present invention. To 2 parts of this dye composition, pure water adjusted to pH 4.5 was added to prepare 3000 parts of a dye bath,
Immerse 100 parts of polyester tropical cloth, 130 ℃
After dyeing for 60 minutes with the dyed product, 6 parts of 45% caustic soda, 6 parts of hydrosulfite, Sanmor RC-7
00 (Nikaka Chemical Co., Ltd., anionic surfactant) 3 parts of water was added to make a total volume of 3000 parts, and reduction washing was performed at 80 ° C. for 10 minutes, washed with water, dried and dyed red. I got a thing. The obtained dyed product had good levels of light fastness, sublimation and water fastness.

【0033】実施例2 式(1)で示される染料原末11部、式(5)で示され
る染料原末15部、式(3)で示される染料原末10部
をデモールN(前述)64部と共にサンドグラインダー
を用いて微粒子化(分散化)し、本発明の染料組成物を
得た。以下実施例1と同様に染色処理し、赤色の染色物
を得た。得られた染色物の耐光、昇華、水堅牢度は実施
例1と同様に良好な水準であった。
Example 2 11 parts of the bulk powder of the formula (1), 15 parts of the bulk powder of the formula (5), and 10 parts of the bulk powder of the formula (3) were added to Demol N (described above). Finely divided (dispersed) together with 64 parts by using a sand grinder to obtain a dye composition of the present invention. The following dyeing treatment was carried out in the same manner as in Example 1 to obtain a red dyed product. The light fastness, sublimation, and water fastness of the obtained dyed product were at the same good level as in Example 1.

【0034】実施例3 式(1)で示される染料原末17部および式(5)で示
される染料原末14部をデモールN(前述)70部と共
にサンドグラインダーを用いて微粒子化(分散化)し、
本発明の染料組成物を得た。以下実施例1と同様に染色
処理し、赤色の染色物を得た。得られた染色物の耐光、
昇華、水堅牢度は実施例1と同様に良好な水準であっ
た。
Example 3 17 parts of the bulk powder of the formula (1) and 14 parts of the bulk powder of the formula (5) were made into fine particles (dispersion) with 70 parts of Demol N (described above) using a sand grinder. ),
A dye composition of the present invention was obtained. The following dyeing treatment was carried out in the same manner as in Example 1 to obtain a red dyed product. Light resistance of the obtained dyed product,
The sublimation and water fastness were at a good level as in Example 1.

【0035】実施例4 式(1)で示される染料原末18部および式(6)で示
される染料原末10部及び式(4)で示される染料原末
5部をデモールN(前述)70部と共にサンドグライン
ダーを用いて微粒子化(分散化)し、本発明の染料組成
物を得た。以下実施例1と同様に染色処理し、赤色の染
色物を得た。得られた染色物の耐光、昇華、水堅牢度は
実施例1と同様に良好な水準であった。
Example 4 18 parts of the bulk powder of the formula (1), 10 parts of the bulk powder of the formula (6) and 5 parts of the bulk powder of the formula (4) were added to Demol N (described above). Fine particles (dispersion) were carried out using 70 parts together with a sand grinder to obtain a dye composition of the present invention. The following dyeing treatment was carried out in the same manner as in Example 1 to obtain a red dyed product. The light fastness, sublimation, and water fastness of the obtained dyed product were at the same good level as in Example 1.

【0036】実施例5 実施例1、実施例2および実施例3で得られた各染料組
成物を2部を含む全量3000部の各染浴をそれぞれ調
製し、2.0デニールのポリエステル加工糸織物50部
と0.14デニールのポリエステル加工糸織物50部を
浸漬し、130℃で60分間染色した後、還元洗浄、水
洗、乾燥した。いずれの染料組成物も2.0デニール糸
織物と0.14デニールの糸織物の同色性に非常に優れ
ていた。
Example 5 A total of 3000 parts of each dyebath containing 2 parts of each of the dye compositions obtained in Examples 1, 2 and 3 was prepared, and 2.0 denier polyester processed yarn was prepared. 50 parts of the woven fabric and 50 parts of the 0.14 denier polyester processed yarn woven fabric were dipped and dyed at 130 ° C. for 60 minutes, then reduced and washed, washed with water and dried. Each of the dye compositions was very excellent in the color uniformity of the 2.0 denier yarn fabric and the 0.14 denier yarn fabric.

【0037】実施例6 実施例1の染料組成物20部に、水380部を加えた
後、ファインガムMC−8(第一工業製薬(株)製、糊
剤)7.5%とソルビトーゼC5(W・Aスコーテルン
社製、糊剤)4.5%、クエン酸0.3%を含む元糊6
00部と練り合わせ、ポリエステルパレス布上に印捺
し、175℃で7分間高温スチーミングを行った後、染
色物をソーダ灰2部、ハイドロサルファイト2部、メイ
サノールBHSニュー(明成化学工業(株)製、非イオ
ン界面活性剤)1部に水を加え全量1000部とした浴
中で、80℃、10分間の還元洗浄を施し、水洗、乾燥
して、赤色の染色物を得た。得られた染色物の耐光、昇
華、水堅牢度は良好な水準であった。
Example 6 To 20 parts of the dye composition of Example 1 was added 380 parts of water, and then 7.5% of fine gum MC-8 (manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd., sizing agent) and sorbitose C5. (Wa Skotern Co., Ltd., sizing agent) 4.5%, citric acid 0.3% original paste 6
After kneading with 00 parts and printing on a polyester palace cloth and performing high-temperature steaming at 175 ° C for 7 minutes, the dyed product is 2 parts soda ash, 2 parts hydrosulfite, Meisanol BHS New (Meisei Chemical Industry Co., Ltd.) Manufactured nonionic surfactant), water was added to 1 part to make a total amount of 1000 parts, reduction washing was performed at 80 ° C. for 10 minutes, washing with water and drying to obtain a red dyed product. The obtained dyed product had good levels of light fastness, sublimation and water fastness.

【0038】[0038]

【発明の効果】本発明の染料組成物を用いた染色法によ
り、太さの異なる繊維が複合化された素材の染色におい
て、優れた均染性および堅牢度が得られるものである。
By the dyeing method using the dye composition of the present invention, excellent levelness and fastness can be obtained in dyeing a material in which fibers having different thicknesses are combined.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】式(1) 【化1】 で示される染料および式(2) 【化2】 (式(2)中、Rは水素または低級アルキル基を示
す。)で示される染料そして必要により式(3) 【化3】 で示される染料および/または式(4) 【化4】 で示される染料を含有してなることを特徴とする赤色分
散染料組成物
1. A formula (1): And a dye represented by the formula (2): (In the formula (2), R represents hydrogen or a lower alkyl group.) And optionally the formula (3) And / or a dye represented by the formula (4): A red disperse dye composition comprising a dye represented by
【請求項2】請求項1において式(1)で示される染料
20〜60重量%、式(2)で示される染料20〜50
重量%、式(3)で示される染料0〜40重量%および
/または式(4)で示される染料0〜20重量%の割合
で配合してなることを特徴とする請求項1記載の分散染
料組成物
2. A dye of the formula (1) according to claim 1 in an amount of 20 to 60% by weight, and a dye of the formula (2) in the range of 20 to 50
2. The dispersion according to claim 1, which is compounded in a proportion of 0 to 40% by weight of the dye represented by the formula (3) and / or 0 to 20% by weight of the dye represented by the formula (4). Dye composition
【請求項3】請求項1または請求項2に記載の分散染料
組成物を用いることを特徴とする疎水性繊維材料の染色
3. A method for dyeing a hydrophobic fiber material, which comprises using the disperse dye composition according to claim 1 or 2.
JP20827494A 1994-02-04 1994-08-10 Red disperse dye composition and method for dyeing hydrophobic fiber material using the same Expired - Fee Related JP3310471B2 (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1305972C (en) * 2004-11-10 2007-03-21 浙江龙盛集团股份有限公司 Composite disperse red dye
CN1309790C (en) * 2004-12-02 2007-04-11 浙江龙盛集团股份有限公司 Composite dispersing dye
JP2008179917A (en) * 2007-01-25 2008-08-07 Teijin Fibers Ltd Method for producing colored polyester fabric, colored polyester fabric and clothing
CN102153887A (en) * 2011-02-24 2011-08-17 浙江万丰化工有限公司 Composite of red disperse dye
CN104945954A (en) * 2015-06-26 2015-09-30 浙江龙盛集团股份有限公司 Disperse red dye composition and dye product

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1305972C (en) * 2004-11-10 2007-03-21 浙江龙盛集团股份有限公司 Composite disperse red dye
CN1309790C (en) * 2004-12-02 2007-04-11 浙江龙盛集团股份有限公司 Composite dispersing dye
JP2008179917A (en) * 2007-01-25 2008-08-07 Teijin Fibers Ltd Method for producing colored polyester fabric, colored polyester fabric and clothing
CN102153887A (en) * 2011-02-24 2011-08-17 浙江万丰化工有限公司 Composite of red disperse dye
CN104945954A (en) * 2015-06-26 2015-09-30 浙江龙盛集团股份有限公司 Disperse red dye composition and dye product

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