JPS5962851A - Developer for diazo copying - Google Patents

Developer for diazo copying

Info

Publication number
JPS5962851A
JPS5962851A JP17483982A JP17483982A JPS5962851A JP S5962851 A JPS5962851 A JP S5962851A JP 17483982 A JP17483982 A JP 17483982A JP 17483982 A JP17483982 A JP 17483982A JP S5962851 A JPS5962851 A JP S5962851A
Authority
JP
Japan
Prior art keywords
developer
silicone oil
boiling point
org
viscosity
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.)
Pending
Application number
JP17483982A
Other languages
Japanese (ja)
Inventor
Hideo Watanabe
秀夫 渡辺
Nobuyoshi Watanabe
信義 渡辺
Norihisa Takahashi
典久 高橋
Masanori Toshimoto
正則 利元
Michiko Umehara
梅原 道子
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.)
Ricoh Co Ltd
Original Assignee
Ricoh 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 Ricoh Co Ltd filed Critical Ricoh Co Ltd
Priority to JP17483982A priority Critical patent/JPS5962851A/en
Publication of JPS5962851A publication Critical patent/JPS5962851A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C5/00Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/18Diazo-type processes, e.g. thermal development, or agents therefor

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)

Abstract

PURPOSE:To obtain developed color images of constant and high density at all times by using a nonpolar org. medium which dissolves a specified org. amine and does not dissolve the components of a photosensitive layer and a produced dye. CONSTITUTION:Org. amine to be used is selected from all of org. amines which are soluble in a nonpolar solvent, have >=150 deg.C, preferably >=170 deg.C b.p., and are liq. at ordinary temp. Silicone oil is used as the nonpolar solvent for dissolving the specified org. amine. Silicone oil is a colorless, nonpolar and oily matter with superior heat and chemical resistances made of straight chain dimethylpolysiloxane. The b.p. and viscosity of silicone oil depend on the mol. wt. The preferred b.p. is >=150 deg.C. The viscosity is not especially restricted, yet silicone oil with excessively high viscosity is not preferably used as the solvent of a developer for diazo copying when spreadability on diazo sensitive paper, permeability and the extent of sticking are taken into consideration.

Description

【発明の詳細な説明】 本発明は有(・幾アミンを用いたジアゾ複写用現像剤の
改良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a diazo copying developer using an amine.

湿式又は半乾式ジアゾ抜写に用いられる現像剤はモノエ
タノールアミン、ジェタノールアミン、ドデシルアミン
等の有機アミンをアルコール、エステル、エーテル、ケ
トン、アミド等の溶媒に溶解したものが普通であるが(
例えば特公昭46−41878号公報)、これら有機溶
媒による人体への影響、揮発性、溶解性、現像性等を考
慮して溶媒として軽油、低級アルコール及びその酢酸エ
ステルからなる混合糸(特公昭48−16842号公報
)、メチルフェニルシリコン、多価アルコール及びクリ
コールエーテルからなる混合系(4′4+、公開51−
14025号公報)を用いたものや、或いはりΣに地肌
部θ)変色μhlFを考慮して溶媒として塩基性窒素原
子を有する有機珪素化合物及び水、アルコール、エーテ
ル、ケトン、エステル、アミド又はスルホキシドからな
る混合系(特開昭52−4828号公報)を用いたもの
が知られている。しかしアルコール、エステル、エーテ
ル、ケトン、アミド等の極性溶媒や水はジアゾ感光紙の
感光層成分であるジアゾ化合物、カップラー、酸安定剤
等や感光層に形成された1jii像成分である染料を溶
精し易いので、こθ)ような46性浴媒そ含む現像r;
すは長時間使用すると、1)その中の塩基成分であるア
ミンは前記溶力IFシた1ν(こよって中和され、現1
ヒj性が低下する結果、召すられる画像は発色不足とな
る、2)極性溶媒が吸湿性なので、環境湿度によって現
懺剤cLt成が稀釈変化し易く、このため画像の発色が
一定しない、3)溶出した染ネ]によって現像剤が汚染
され、従って才だコピーの地肌も汚染される、リフビー
後も支持体中に残留する極性溶媒によって染料画像が退
色し易い等の欠点を生じる。
The developer used for wet or semi-dry diazo copying is usually one in which organic amines such as monoethanolamine, jetanolamine, and dodecylamine are dissolved in solvents such as alcohols, esters, ethers, ketones, and amides.
For example, Japanese Patent Publication No. 46-41878 (Japanese Patent Publication No. 46-41878), a mixed yarn consisting of light oil, lower alcohol, and its acetate ester as a solvent (Japanese Patent Publication No. 48 -16842 Publication), a mixed system consisting of methylphenyl silicone, polyhydric alcohol and glycol ether (4'4+, Publication No. 51-
14025 Publication), or an organosilicon compound having a basic nitrogen atom as a solvent, and water, alcohol, ether, ketone, ester, amide, or sulfoxide, taking into consideration the discoloration μhlF of the background part θ). A system using a mixed system (Japanese Unexamined Patent Publication No. 52-4828) is known. However, polar solvents such as alcohols, esters, ethers, ketones, and amides, and water dissolve the diazo compounds, couplers, acid stabilizers, etc. that are the components of the photosensitive layer of diazo photosensitive paper, and the dyes that are the 1JII image components formed on the photosensitive layer. Because it is easy to clean, development r containing 46-based bath medium such as θ);
When used for a long time, 1) the amine, which is the base component therein, is neutralized and becomes
As a result of the reduced heat resistance, the resulting image will lack color development; 2) Since the polar solvent is hygroscopic, the composition of the printing agent cLt is likely to change in dilution depending on the environmental humidity, and as a result, the color development of the image will not be constant; 3) ) The developer is contaminated by the eluted dye, and therefore the background of the printed copy is also contaminated, and the dye image tends to fade due to the polar solvent remaining in the support even after rifling.

本発明の第一の目的は特定の有機アミンは溶解するが、
感光層成分や生成染料を溶解しない非極性有機媒体を用
いることにより、現像剤やコピーの地肌の変色や汚染の
みならず、染料画像の退色もなく、常に一定の高濃度発
色画像が得られるジアゾ複写用現像剤を提供することで
ある。
The first object of the present invention is to dissolve certain organic amines, but
By using a non-polar organic medium that does not dissolve the components of the photosensitive layer or the dye produced, diazo produces consistently high-density colored images without causing discoloration or contamination of the developer or copy background, as well as fading of the dye image. An object of the present invention is to provide a developer for copying.

本発明の第二の目的は環境温度や湿贋に影響されない安
定なジアゾ複写用現像剤を提供することである。
A second object of the present invention is to provide a stable diazo copying developer that is not affected by environmental temperature or moisture or forgeries.

即ち本発明の現像剤は沸点150℃以上の液状有機アミ
ンをシリコンオイルに溶解してなるものである。
That is, the developer of the present invention is prepared by dissolving a liquid organic amine having a boiling point of 150° C. or higher in silicone oil.

本発明で使用される有機アミンは非極性溶媒に溶解する
沸点150℃以上、奸才しくは170℃以上の常温で液
状のものであれば全て使用できる。沸点150℃以下で
は蒸発して現像剤の組成を変化させるし、才た常温で固
形のものを用いると、溶媒中で析出し易< 、現ih!
剤として使用できなくなる。なお従来使用されて来たア
ルコールアミン等の有機アミンは大部分、非極性溶媒に
溶けないので、本発明では殆んど使用できない。
Any organic amine used in the present invention can be used as long as it dissolves in a nonpolar solvent and is liquid at room temperature with a boiling point of 150° C. or higher, preferably 170° C. or higher. If the boiling point is below 150°C, it will evaporate and change the composition of the developer, and if you use a developer that is solid at room temperature, it will easily precipitate in the solvent.
It can no longer be used as an agent. It should be noted that organic amines such as alcohol amines that have been conventionally used are mostly insoluble in non-polar solvents, so they can hardly be used in the present invention.

本発明で使用される前述のような性状の有機アミンとし
てはn−へジチルアミン(沸点158.3℃)、n−オ
クチルアミン(沸点188℃)、n−デシルアミン(沸
点217℃)、2−エチルヘキシルアミン(沸点169
℃)、メチルイミノビスプロピルアミン(沸点234℃
)、ジプロピレントリアミン(沸点240℃)、ジエチ
ルアミノプロビルアミン(沸点169℃)、ジブチルア
ミノプロビルアミン(沸点238℃)、N−(アミノプ
ロピル)モルホリン(沸点21s〜230℃)、N−(
アミノゾロビル)−2−ピコヘリン(沸点22+1℃)
、N−アミノエチルピペリジン(沸点182℃)、N−
アミノエチルモルホリン(沸点200℃)、”+”−ビ
スアミノメチルシクロヘキサン(7wHgでの沸点10
8℃)、ジエチレントリアミン(沸点206、7℃)、
トリエチレンテトラミン(沸点277℃)、テトラエチ
レンペンタミン(沸点340℃)、ヘンタエチレンへキ
サミン(50ttanHg テノ沸点260℃)、ジシ
クロヘキシルアミン(沸点256℃)、ジベンジルアミ
ン(沸点215℃)、ジブチルアミン(沸点169℃)
、n−トリブチルアミン(沸点214℃)、シアミルア
ミン(沸点202℃)、ジオクチルアミン(沸点297
℃)、ブトキシプロピルアミン(沸点176℃)、イン
クトキシプロピルアミン(沸点160℃)、2−エチル
へキシロイルプロピルアミン(100mHgでの沸点1
60℃)、1.4−ジアミノブタン(沸点158℃)等
が挙げられる。なおこれらの中でも発色性の点から塩基
性の萬い一級アミンが好ましい。才だこれら有機アミン
の使用量は非極性溶媒に対する溶解度にもよるが、一般
には現像剤に対し5〜95重)11チ、好ましくは20
〜80重量%の範囲である。5 M(、”J: %以下
ではアルカリとしての計が少ないので発色不足になる。
Examples of the organic amines having the above properties used in the present invention include n-heditylamine (boiling point 158.3°C), n-octylamine (boiling point 188°C), n-decylamine (boiling point 217°C), and 2-ethylhexyl. Amine (boiling point 169
°C), methyliminobispropylamine (boiling point 234 °C)
), dipropylene triamine (boiling point 240°C), diethylaminopropylamine (boiling point 169°C), dibutylaminopropylamine (boiling point 238°C), N-(aminopropyl)morpholine (boiling point 21s-230°C), N-(
Aminozolovir)-2-picohelin (boiling point 22+1℃)
, N-aminoethylpiperidine (boiling point 182°C), N-
Aminoethylmorpholine (boiling point 200°C), “+”-bisaminomethylcyclohexane (boiling point 10 at 7wHg)
8°C), diethylenetriamine (boiling point 206, 7°C),
Triethylenetetramine (boiling point 277°C), tetraethylenepentamine (boiling point 340°C), hentaethylenehexamine (50ttanHg teno boiling point 260°C), dicyclohexylamine (boiling point 256°C), dibenzylamine (boiling point 215°C), dibutylamine (boiling point 169℃)
, n-tributylamine (boiling point 214°C), cyamylamine (boiling point 202°C), dioctylamine (boiling point 297°C)
), butoxypropylamine (boiling point 176°C), ink toxypropylamine (boiling point 160°C), 2-ethylhexyloylpropylamine (boiling point 1 at 100 mHg)
60°C), 1,4-diaminobutane (boiling point 158°C), and the like. Among these, basic primary amines are preferred from the viewpoint of color development. The amount of these organic amines to be used depends on their solubility in non-polar solvents, but is generally 5 to 95 times (11 times), preferably 20 times, relative to the developer.
~80% by weight. If it is less than 5 M(, "J:%"), there will be less amount of alkali, resulting in insufficient color development.

また95重情係以上では液粘度が低くなり易く、感光紙
への浸透性が強く、画像砲度を低下させる上、画像退色
にも悪影響を与える。
Further, if the liquid is more than 95%, the liquid viscosity tends to be low, and the permeability into the photosensitive paper is strong, lowering the image clarity and having an adverse effect on image fading.

一方、以上のような特定の有機アミンを溶解する非極性
溶媒として本発明ではシリコンオイルが使用される。シ
リコンオイルは周知のように直鎖状ジメチルポリシロキ
サンからなる特lこ耐熱性及び耐薬品性に優れた無色の
非極性油状物質である。このものは分子址の大きさによ
って沸点や粘度か異なるが、沸点については本発明では
有4羨アミンの場合と同様な理由から150℃以上のも
のが好ましい。粘度については特別な制限はないが、ジ
アゾ複写用現像剤の溶媒としてジアゾ感光紙への延展性
、滲透性、付着量等を考lがすると余り高粘度のものは
好ましくない。そこで高粘度のシリコンオイルを用いる
場合はジアゾ複写用現像剤として適切な粘度となるよう
に他の低粘度シリコンオイルや他の低粘度非極性溶媒を
併用すると良い。なおこ\で使用される他の低粘度非極
性溶媒としては前述のような理由から150℃以上の高
沸点のものが好ましく、例えばパラフィン系、イソパラ
フィン系、ナフテン系又は芳香族系炭化水素溶媒がある
On the other hand, in the present invention, silicone oil is used as a nonpolar solvent for dissolving the above-described specific organic amine. As is well known, silicone oil is a colorless, non-polar oily substance made of linear dimethylpolysiloxane that has particularly excellent heat resistance and chemical resistance. The boiling point and viscosity of this substance differ depending on the size of the molecular mass, but in the present invention, a boiling point of 150° C. or higher is preferred for the same reason as in the case of the amine. There are no particular restrictions on the viscosity, but when considering spreadability, permeability, adhesion amount, etc. to diazo photosensitive paper as a solvent for a developer for diazo copying, a solvent with too high a viscosity is not preferred. Therefore, when using a high viscosity silicone oil, it is recommended to use another low viscosity silicone oil or another low viscosity nonpolar solvent in combination so that the viscosity is suitable for a developer for diazo copying. Other low viscosity non-polar solvents used in Naoko\ are preferably those with a high boiling point of 150°C or higher for the reasons mentioned above, such as paraffinic, isoparaffinic, naphthenic or aromatic hydrocarbon solvents. .

以上のような成分からなる本発明の現像剤はジアゾ感光
紙を現像剤中に浸漬塗布する湿式ジアゾ現像法やジアゾ
感光紙にロール転写により微J<)塗布する半乾式ジア
ゾ現像法のいずれにも適用できる。なお現像剤は現像を
促進するため、必苅あれば加熱して用いる。
The developer of the present invention comprising the above-mentioned components can be used in either a wet diazo development method in which diazo photosensitive paper is coated by dipping in the developer or a semi-dry diazo development method in which a fine coating is applied to diazo photosensitive paper by roll transfer. can also be applied. Note that the developer is heated if necessary to accelerate development.

以下に本発明を実施例により説明する。なお俤は全て重
積チである。
The present invention will be explained below using examples. Note that all of the tai are stacked ts.

実施例1 n−オクチルアミン40%及びシリコンオイル60チ(
信越シリコーンKF−96−1+10 )を混合して粘
度25センチポイズ(20℃) (1)ジアゾ複写用現
像剤を調製した。
Example 1 40% n-octylamine and 60% silicone oil (
(1) A developer for diazo copying was prepared by mixing Shin-Etsu Silicone KF-96-1+10) with a viscosity of 25 centipoise (20 DEG C.).

次にこの現像液をロール転写により露光済の市販θ〕2
成分系ジアゾ感光紙lこ做鼠塗布(感光紙への付’jf
q−%fで/ 4omy/ A −4版)したところ、
画像濃度1.21の画像が得られた。またこの画像につ
いてフェードメーターにより強制劣化試験(スガ試kk
 機KK5Mロングライフフェードメーター1” A 
−3型を用いて3時間光照射)を行なって画像の退色性
を調べた。一方、比較θ)ため市販のジアゾ複写用現像
剤(モノエタノールアミン20チ、エチレングリコール
40チ及びメチルカルビノール40%よりなる)につい
ても同様に現像し、節制劣化テストを行なった。
Next, this developer was applied to the exposed commercially available θ〕2 by roll transfer.
Component-based diazo photosensitive paper coating (applying to photosensitive paper)
q-%f/4omy/A-4 version),
An image with an image density of 1.21 was obtained. In addition, this image was subjected to a forced deterioration test (Suga Test KK) using a fade meter.
Machine KK5M Long Life Fade Meter 1” A
-3 type was used for 3 hours of light irradiation) to examine the discoloration of the image. On the other hand, for comparison θ), a commercially available developer for diazo copying (consisting of 20% monoethanolamine, 40% ethylene glycol, and 40% methyl carbinol) was developed in the same manner and subjected to a restraint deterioration test.

以上の結果は表−1の通りである一 表−1 江)  Dmax  :テスト前の画像0度D’max
  :テスト後の画蹟敲度 △Dmax  :テスト後の画像諷度低下量このように
本発明品は退色性が非常薔こ優れている。
The above results are shown in Table-1.
: Paint sharpness after test △Dmax : Amount of decrease in image sharpness after test As described above, the product of the present invention has excellent discoloration resistance.

実施例2 ジシクロヘキシルアミン50%及びシリコンオイル(信
越シリコーンI(F−96−300)50%を混合して
粘度25センチポイズ(20℃)のジアゾ複写用現像剤
を調製した。
Example 2 A diazo copying developer having a viscosity of 25 centipoise (20 DEG C.) was prepared by mixing 50% dicyclohexylamine and 50% silicone oil (Shin-Etsu Silicone I (F-96-300)).

次にこの現像剤を70℃lこ加熱しな力5ら実施例1と
同様に現像し、更に強制劣化テストを行なってDmax
=1.24 、D’max=1.15の結果を得た。
Next, this developer was heated to 70°C and developed in the same manner as in Example 1.
= 1.24 and D'max = 1.15.

実施例3 n−アミノゾロビルモルホリン20%、ジベンジルアミ
ンlD%、シリコンオイル(トーレシリコーン81(2
00−20+1 )60チ及び沸点17゛4〜189℃
のイソ7ぞラフイン糸炭イヒ水素溶媒(アイソパーH)
 10%を混合して粘度28センチボイズ(20℃)の
ジアゾ複写用現1辣ulを調製した。以下、この現像剤
を用0て実施秒1j1と同様に現像し、強制劣化テスト
を行なってDmax=1.22 、 D’max==1
.16の結果を得た。またこの現イ象液と実MQ例1で
用いた比較用現像液を用いて市販の2成分系ジアゾ感光
紙(大きさA−4版) I n o n枚について連続
コピーを行ない、コピーの画体♂ユ度及び地肌一度、並
びIこコピー後の現f8ヒ液の状態を比較し、表−20
〕結果を得た。
Example 3 20% n-aminozolobyl morpholine, 1D% dibenzylamine, silicone oil (Toray Silicone 81 (2
00-20+1) 60 degrees and boiling point 17゛4-189℃
Iso 7 Rough-in yarn Carbohydrogen solvent (Isopar H)
A diazo copying liquid having a viscosity of 28 centivoise (20° C.) was prepared by mixing 10% of the above ingredients. Hereinafter, development was carried out using this developer in the same manner as in Example 1j1, and a forced deterioration test was performed to obtain Dmax=1.22 and D'max==1.
.. 16 results were obtained. In addition, using this developing solution and the comparative developer used in Actual MQ Example 1, continuous copying was carried out on one sheet of commercially available two-component diazo photosensitive paper (size A-4 version), and the results of the copies were evaluated. Comparing the image quality and background, as well as the condition of the current f8 liquid after copying, Table 20
] Obtained the results.

表−2 注)  Dmin:地肌濃度 このようζこ本発明品は液の安定性が良く、大itにコ
ピー後も画像鋲度を低下させず、また地肌も汚さない。
Table 2 Note) Dmin: Background density The product of the present invention has good liquid stability, does not reduce image tackiness even after being copied to a large size, and does not stain the background.

Claims (1)

【特許請求の範囲】[Claims] 1、節点150℃以上の液状有機アミンをシリコンオイ
ルに溶解してなるジアゾ複写用現像剤。
1. A diazo copying developer prepared by dissolving a liquid organic amine with a nodal point of 150°C or higher in silicone oil.
JP17483982A 1982-10-04 1982-10-04 Developer for diazo copying Pending JPS5962851A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17483982A JPS5962851A (en) 1982-10-04 1982-10-04 Developer for diazo copying

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17483982A JPS5962851A (en) 1982-10-04 1982-10-04 Developer for diazo copying

Publications (1)

Publication Number Publication Date
JPS5962851A true JPS5962851A (en) 1984-04-10

Family

ID=15985552

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17483982A Pending JPS5962851A (en) 1982-10-04 1982-10-04 Developer for diazo copying

Country Status (1)

Country Link
JP (1) JPS5962851A (en)

Similar Documents

Publication Publication Date Title
US3578452A (en) Developing compositions for diazotype materials
JPH1184581A (en) Image formed photographic element
JPH0430355B2 (en)
AU2007263607B2 (en) Composition, article, its manufacture and use
JPH0126352B2 (en)
JPS5962851A (en) Developer for diazo copying
JPH0411396B2 (en)
US2843481A (en) Photographic processes
JP2529882B2 (en) Diazo correction image erasing solution
US3907567A (en) Waxy crayon or ink-like diazotype developer composition comprising heat transferrable azo coupler and transfer promotor
JP3980119B2 (en) Ink jet recording material
JPS58172646A (en) Heat development type diazo copying material
JPS58134639A (en) Solution for correcting silver salt lithographic plate
JPS588690A (en) Heat-sensitive recorder capable of fixing multi-color formation
JPS5913015B2 (en) Diazotype material and image reproduction method using it
JPH0220434B2 (en)
JPS5853485A (en) Light sensitive and heat-sensitive composition
JPH02235685A (en) Thermally sensitive recording material
JPS6125136A (en) Negative type diazo copying material and its fixing method
Priest Pyronin Y for staining stripped autoradiographs prepared from plastic embedded sections of rat tissues containing plutonium
JPS62207673A (en) Diazo fixation type thermal recording material
US3918974A (en) Process for the diazo-type multicolor reproduction
JPH0241434B2 (en)
JPS60159745A (en) Developer for diazo copying
JPS62253487A (en) Diazo heat sensitive recording material