JPS5982480A - Dyeing method - Google Patents

Dyeing method

Info

Publication number
JPS5982480A
JPS5982480A JP58176719A JP17671983A JPS5982480A JP S5982480 A JPS5982480 A JP S5982480A JP 58176719 A JP58176719 A JP 58176719A JP 17671983 A JP17671983 A JP 17671983A JP S5982480 A JPS5982480 A JP S5982480A
Authority
JP
Japan
Prior art keywords
water
resin
dye
dyeing method
dyed
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
JP58176719A
Other languages
Japanese (ja)
Other versions
JPS6142038B2 (en
Inventor
吉田 兼紀
達夫 正木
熊谷 広次
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.)
Toppan Inc
Original Assignee
Toppan Printing 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
Application filed by Toppan Printing Co Ltd filed Critical Toppan Printing Co Ltd
Priority to JP58176719A priority Critical patent/JPS5982480A/en
Publication of JPS5982480A publication Critical patent/JPS5982480A/en
Publication of JPS6142038B2 publication Critical patent/JPS6142038B2/ja
Granted legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 これな主要モノマー成分とする樹脂への染色方法に関す
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for dyeing resin as a main monomer component.

ヒドロキンメククリレート位1脂は.ヒトロキシル基?
有する分子構造により水に不溶性でありながら吸温性お
よび水膨潤性がきわめてすぐhた樹脂として特徴がある
。そして、従来からこの樹脂をフィルム、膜、成形物な
どに加工し、こつ性質な生かした応用物がいくつか開発
されている。これらはそitぞtl.用途に応じて染色
したり.文字、絵柄等の両像な印idlする必要が当然
生ずる。しかしながら、このi1脂の特性から、水ある
いtま水蒸気の雰囲気の中で使わ才するため,通常の油
性インキによる印刷″Cま不可能であり.また水性のイ
ンキまた1lま染色液を用いて印刷,染色できても.そ
の画像は樹脂が水で膨潤するため染着されず溶出してし
まう。
Hydroquine mech acrylate position 1 fat is. Hydroxyl group?
Due to its molecular structure, it is characterized as a resin that is insoluble in water but has extremely high heat absorption and water swelling properties. Since then, this resin has been processed into films, membranes, molded products, etc., and several applications have been developed that take advantage of its unique properties. These are the tl. It can be dyed depending on the purpose. Naturally, there arises a need to provide both types of marks such as characters and pictures. However, due to the characteristics of this i1 fat, it is used in an atmosphere of water or steam, so it is impossible to print with ordinary oil-based ink. Even if the image can be printed and dyed, the resin will swell with water, so the image will not be dyed and will be eluted.

従来から試みられている例ヤ挙げると.例えばヒドロキ
シメタクリレート樹脂な水M性染料溶液に接触させると
容易に染色され鮮明な両1象が得られるが.こhl水中
に長く保存すると次第に染料が溶出し、lli!ii@
が消えてしまう。また、油性溶剤中に染料、顔料、バイ
ンダー樹脂等な溶解、分散させた一般的なインキにてこ
の(支)1形成品表面に印刷すると一時的に(ま鮮明に
印刷できても、水中に長く保存するとインキの接着力が
弱くなり、印刷画@)fま次第にう丁(なる。以上の例
のように、ヒドロキンメタクリレート樹脂製品−\の印
刷、染色な行なう場合、普通に考えら)するインキの接
着力な利用する方法や、樹脂への単なる染色による方法
Itま不適当であることが明らかとなった。
Here are some examples of what has been attempted in the past. For example, when it is brought into contact with a water-based dye solution such as hydroxy methacrylate resin, it is easily dyed and a clear pattern can be obtained. If you keep it in water for a long time, the dye will gradually elute and lli! ii@
disappears. In addition, if you print on the surface of this (support) 1 product with a general ink containing dissolved or dispersed dyes, pigments, binder resins, etc. in an oil-based solvent, it may be temporarily (even if you can print clearly) If stored for a long time, the adhesive strength of the ink will weaken, and the printed image will gradually become sticky.As in the above example, when printing or dyeing a hydroquine methacrylate resin product, it is normal to think about it. It has become clear that methods that utilize the adhesive strength of ink and methods that simply dye the resin are inappropriate.

本発明はこの点な考慮t2て鋭意研究の結果成されたも
のであり、その要旨とするところは、ヒドロギシエチル
メタアクリレートまた1fまこht主要なモノマー成分
とする樹脂への染色方法において、該樹脂の所望の部分
に感光性な有する水可溶性バ露光することを特徴とする
染色方法であり、従来の欠点な原理的に解消するきわめ
て有効な方法であって、この発明の基本となる水不溶化
処理により、染料が樹脂の高分子網目構造内にからまり
、樹脂を水で膨潤させても流ib出丁ことがなく、極め
て安定な染着側1象な形成することができる。
The present invention has been achieved as a result of intensive research in consideration of this point, and its gist is to provide a dyeing method for resins in which hydroxyethyl methacrylate or 1F machoht is the main monomer component. This dyeing method is characterized by exposing a desired part of the resin to light using a photosensitive water-soluble resin, and is an extremely effective method that fundamentally overcomes the drawbacks of the conventional method, and is the basis of this invention. As a result of the treatment, the dye is entangled within the polymer network structure of the resin, and even when the resin is swollen with water, it does not run out, making it possible to form an extremely stable dyed side.

次に本発明のさらに具体的な説明なする。Next, a more specific explanation of the present invention will be given.

まず、水可溶性バット染料ロイコ体であるが、この染料
’l’!−周知のとおり、バット染¥4 k還元し。
First of all, it is a water-soluble vat dye leuco type, and this dye 'l'! -As you know, bat dyeing costs ¥4k.

スルホン酸塩とした水浴性化合物でこのままでIl’L
酸化反応を起す染料がある。このような感光性のある水
可溶性バット染料ロイコ体としてl、ま1例えば、5o
lubi I 1sed vat yel low 3
 、4.7.8゜Red  1.2J′10、BIue
2 、 5 、 8 、 Black  1.4.6等
がある。
Il'L as it is with a water-bathable compound as a sulfonate.
There are dyes that cause oxidation reactions. Such photosensitive water-soluble vat dye leuco bodies include l, or, for example, 5o.
lubi I 1sed vat yel low 3
, 4.7.8°Red 1.2J'10, BIue
2, 5, 8, Black 1.4.6, etc.

この染料な含む染色液また11まインキな用いて削記耐
脂と接触させると、この染料ばその親和性により樹脂内
に浸透する。その後、この樹脂をその中に浸透している
染料が吸収する光で露光すると。
When a staining liquid or ink containing this dye is brought into contact with the abrasion resistant material, the dye penetrates into the resin due to its affinity. This resin is then exposed to light that is absorbed by the dye that has penetrated into it.

染料の水不溶化ならびに発色化反応が明脂内で起こり、
極めて安定し7た両像が形成さ1する。染色液。
The water insolubilization of the dye and the coloring reaction occur within the clear resin,
Very stable images are formed. Staining solution.

インキとするためにこの染料の他に安定剤、印刷適性な
向上させる添加剤を水に適宜加起る。
In addition to this dye, a stabilizer and additives for improving printability are appropriately added to water to form an ink.

以下実施例について説明1−る。Examples will be explained below.

〈実施例1〉 2−ヒドロキシエチルメタアクリレート樹脂から成る透
明フィル1.に溶性バント染料アンソラゾール04G(
ヘキスト社製)水溶液(a度60!//p)に10分間
−浸−漬(下漬け)シ、これなとり出し1表面に付着し
た溶液な除去した後、 Be’硫酸(濃度約1occ/
a)、sよび亜硝酸ソーダ(濃度約o、 s g/B)
な水に溶かした溶液(発色浴)に15分間浸漬すると、
フィルムは均一に青色に染色できた。その後、このフィ
ルムな充分水洗し、来反応の染料な洗い落した。
<Example 1> Transparent film made of 2-hydroxyethyl methacrylate resin 1. Vandt dye Anthorazole 04G (soluble in
Hoechst Co., Ltd.) aqueous solution (A degree 60!//p) for 10 minutes.
a), s and sodium nitrite (concentration approx. o, s g/B)
When immersed in a solution dissolved in water (coloring bath) for 15 minutes,
The film could be uniformly dyed blue. Thereafter, the film was thoroughly washed with water to wash away the dye from the subsequent reaction.

この透明フィルム上に、2kVi水銀灯から透過原稿な
通して画(8)を投影すると鮮明な青色画像が形成さt
tた。その後、このフィルムな温湯で充分煮沸し、非画
像部の染*8+な溶出した。この方法で染色しlこフィ
ルム゛の染着性を調べるためにこのフィルムを沸騰水中
で数時間煮沸(堅牢試験)したが。
When image (8) is projected onto this transparent film through a transparent original from a 2 kVi mercury lamp, a clear blue image is formed.
It was. Thereafter, the film was sufficiently boiled in hot water to elute the dye *8+ in the non-image area. In order to examine the dyeability of the film dyed by this method, the film was boiled in boiling water for several hours (fastness test).

色が薄くなることなく、堅牢な染着ができたことが確め
らhた。なお、その他の感光性を有する水可溶性バット
染料ロイコ体を用いて同様の操作で染着したところ、は
ぼ同様の結果な得た。
It was confirmed that strong dyeing was achieved without the color becoming light. In addition, when dyeing was carried out in the same manner using other photosensitive water-soluble vat dye leuco bodies, similar results were obtained.

〈実施例2〉 架橋型2−ヒドロキシエチルメタアクリレート樹脂より
加工されたソフトコンタクトレンズは生理食塩水中に浸
漬して膨潤させである。このレンズを取出l−表面の水
な除去した後、レンズの周辺(〜 近傍の所定の位置  溶性バット染料アントラゾールピ
ンク16B(ヘキスト社製)6部、グリセリン16部、
水14部から成るインキな含浸させた多孔性、スポンジ
ラバー製ゴム印にて文字を印字した。その後、このレン
ズをプラノクライト(光量2 、、WΔ)にて約1分間
露光すると鮮明な赤色の文字が発色してきた。この染着
文字Itま実施例1と同様の堅牢試験に充分耐えた。
<Example 2> A soft contact lens processed from cross-linked 2-hydroxyethyl methacrylate resin was immersed in physiological saline to swell. After removing this lens and removing water from the surface, apply 6 parts of soluble vat dye Anthrazol Pink 16B (manufactured by Hoechst), 16 parts of glycerin,
The letters were printed with a porous, sponge rubber stamp impregnated with an ink consisting of 14 parts of water. Thereafter, when this lens was exposed to planocrite (light intensity 2, WΔ) for about 1 minute, clear red letters developed. This dyed letter It sufficiently withstood the same fastness test as in Example 1.

〈実施例3〉 実施例2に示すレンズの周辺近傍の所定の一部分に実施
例2に示す組成のインキな塗布した。その後、塗布さJ
tた部分に2 kW水銀灯から透過ネガ原稿を通して約
2分間文字像を投影すると鮮明な赤色の文字が発色して
きた。その後このレンズな温湯中に浸漬し、未発色部分
の染柄なレンズ内から溶出した。このようにして形成さ
れた染着文字シま実施例1と同様の堅牢試験に充分耐え
た。
<Example 3> An ink having the composition shown in Example 2 was applied to a predetermined portion near the periphery of the lens shown in Example 2. Then applied J
When a character image was projected for about 2 minutes through a transparent negative original from a 2 kW mercury lamp onto the area where the image was exposed, clear red characters appeared. The lens was then immersed in warm water, and the uncolored parts of the lens were eluted. The dyed letter stripes thus formed satisfactorily withstood the same fastness test as in Example 1.

なお、実施例2,3について、その他の感光性な有する
水町d性バット染刺ロイコ体を用いても同様の結果が得
られた。
In Examples 2 and 3, similar results were obtained using other photosensitive Mizumachi d-type bat-dyed leuco bodies.

特許出願人 凸版印刷株式会社 代表者鈴木和夫patent applicant Toppan Printing Co., Ltd. Representative Kazuo Suzuki

Claims (1)

【特許請求の範囲】[Claims] (1)  ヒドロキシエチルメタアクリレートマたはこ
t’L f主要なモノマー成分とする樹脂への染色方法
において、該泣1脂の所望の部分に感光性を有す吸収す
る光で露光することな特徴とする染色方法。 (2、特許請求の範囲第1項において、感光性な有する
水可溶性バット染料ロイコ体な含有するインキなヒドロ
キシメタクリレート樹脂から成るソフトコンタクトレン
ズの所望の位置に浸透させた後、該レンズケ該感光性?
有する水可溶性バット染料ロイコ体が吸収する光で露光
することな特徴とする染色方法。
(1) Hydroxyethyl methacrylate polymer or t'Lf In the dyeing method for the resin that is the main monomer component, the desired part of the resin is not exposed to absorbing light that has photosensitivity. Characteristic dyeing method. (2. In claim 1, after infiltrating into a desired position of a soft contact lens made of a hydroxy methacrylate resin, an ink containing a photosensitive water-soluble vat dye and a leuco compound, ?
A dyeing method characterized by exposing to light absorbed by a water-soluble vat dye leuco body.
JP58176719A 1983-09-24 1983-09-24 Dyeing method Granted JPS5982480A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58176719A JPS5982480A (en) 1983-09-24 1983-09-24 Dyeing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58176719A JPS5982480A (en) 1983-09-24 1983-09-24 Dyeing method

Publications (2)

Publication Number Publication Date
JPS5982480A true JPS5982480A (en) 1984-05-12
JPS6142038B2 JPS6142038B2 (en) 1986-09-18

Family

ID=16018572

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58176719A Granted JPS5982480A (en) 1983-09-24 1983-09-24 Dyeing method

Country Status (1)

Country Link
JP (1) JPS5982480A (en)

Also Published As

Publication number Publication date
JPS6142038B2 (en) 1986-09-18

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