NO138049B - PROCEDURES FOR DIAZO COPYING USING SMOODS DEVELOPERS AND AMINIDE DEVELOPERS FOR SUCH USES - Google Patents
PROCEDURES FOR DIAZO COPYING USING SMOODS DEVELOPERS AND AMINIDE DEVELOPERS FOR SUCH USES Download PDFInfo
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- NO138049B NO138049B NO987/72A NO98772A NO138049B NO 138049 B NO138049 B NO 138049B NO 987/72 A NO987/72 A NO 987/72A NO 98772 A NO98772 A NO 98772A NO 138049 B NO138049 B NO 138049B
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- Prior art keywords
- alkyl
- liquid
- weight
- developing
- alkylolalkoxy
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- 238000000034 method Methods 0.000 title claims description 11
- -1 DIAZO Chemical class 0.000 title claims description 9
- 239000007788 liquid Substances 0.000 claims description 27
- 239000000463 material Substances 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 239000003085 diluting agent Substances 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 9
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- 239000000194 fatty acid Substances 0.000 claims description 8
- 150000004665 fatty acids Chemical class 0.000 claims description 8
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 230000001105 regulatory effect Effects 0.000 claims description 6
- 150000005846 sugar alcohols Polymers 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 239000000987 azo dye Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 230000005855 radiation Effects 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 5
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 4
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 229940051250 hexylene glycol Drugs 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 206010028347 Muscle twitching Diseases 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- DTOSIQBPPRVQHS-UHFFFAOYSA-N α-Linolenic acid Chemical compound CCC=CCC=CCC=CCCCCCCCC(O)=O DTOSIQBPPRVQHS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/18—Diazo-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)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Developing Agents For Electrophotography (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
Nærværende oppfinnelse vedrører en fremgangsmåte for reproduksjon av en ^original på et tokomponent-diazotype-kopieringsmateriale og en fremkallingsvæske for anvendelse ved fremgangsmåten hvor den aktive komponent er et organisk amin. Nærmere bestemt vedrører oppfinnelsen en fremkallingsvæske, som kan anvendes under betingelser hvorved små mengder av væsken fordeles over den latent-billed-bærende overflaten av et tokomponent-materiale av diazotypen. The present invention relates to a method for reproducing an original on a two-component diazotype copying material and a developing liquid for use in the method where the active component is an organic amine. More specifically, the invention relates to a developing liquid, which can be used under conditions whereby small amounts of the liquid are distributed over the latent-image-bearing surface of a two-component material of the diazo type.
Diazotype-reproduksjonsprosesser, hvorved et tokomponent-diazotype-materiale fremkalles ved påforing av en liten mengde fremkallingsvæske, som vanligvis ikke overstiger 3 g pr. m av overflaten som bærer det latente bilde, beskrives i det amerikanske patentskriftet 3.446.620. Denne kjente teknikk, som gir en torr kopi direkte fra et fremkallingstrinn, utfores ved at man overforer en reguler t mengde av 3en konsentrerte f rem-kallingslosningen, hvilken inneholder et alifatisk amin, til et tokomponent-diazotype-materiale. Nevnte teknikk krever en fremkallingssone gjennom hvilken det eksponerte diazotype-papiret fores, og hvorved den regulerte mindre mengden væske direkte påfores overflaten som bærer et latent bilde av diazotype for effektivt å fremkalle azofargebildet, og kopien erholdes torr, luktfri og ferdig til bruk. Diazotype reproduction processes, whereby a two-component diazotype material is developed by applying a small amount of developing fluid, usually not exceeding 3 g per m of the surface that carries the latent image is described in US Patent No. 3,446,620. This known technique, which provides a dry copy directly from a developing step, is carried out by transferring a regular amount of the 3en concentrated developing solution, which contains an aliphatic amine, to a two-component diazo type material. Said technique requires a developing zone through which the exposed diazotype paper is fed, whereby the regulated minor amount of liquid is directly applied to the surface bearing a latent image of diazotype to effectively develop the azo color image, and the copy is obtained dry, odorless and ready for use.
De regulerte væskemengdene innebærer påforing av mengder som The regulated quantities of liquid involve the application of amounts which
ikke overstiger 3 g fremkaller pr. m 2 av den billedbærende overflaten, fortrinnsvis ca. 0,5 - 2 g/m 2. does not exceed 3 g developer per m 2 of the image-bearing surface, preferably approx. 0.5 - 2 g/m 2.
Den metode som beskrives i det amerikanske patentskriftet 3.446.620 kan utfores ved hjelp av et antall forskjellige typer anordninger som er spesielt tilpasset til påforing av regulerte mengder. The method described in US patent document 3,446,620 can be carried out using a number of different types of devices which are specially adapted to the application of regulated amounts.
En slik anordning beskrives i det amerikanske patentskriftet 3.626.833. Det bor legges merke til at ved en slik fremkallingsanordning anvendes ikke den vanlige rutinemessige teknikken for påforing av en væske, men man må ta spesielle hensyn i betrakt-ning. Such a device is described in US patent document 3,626,833. It should be noted that with such a developing device the usual routine technique for applying a liquid is not used, but special considerations must be taken into account.
Når en flytende fremkaller påfores i en mengde på 1 eller 2 g/m<2 >overflate av tokomponent-diazotype-materialet, så er det nodvendig at væsken i fremkallingssonen påfores jevnt fordelt på When a liquid developer is applied in an amount of 1 or 2 g/m<2 >surface of the two-component diazo type material, it is necessary that the liquid in the development zone is applied evenly distributed on
en slik måte at det erholdte azofarge-bildet oppviser en enhetlig fargetetthet. Det har også vist seg at anordningen som påfører de regulerte mengdene fremkaller u-tréettes for s-fcore påkjenninger, og fremkalleren må fordeles jevnt over heie den billedbærende overflaten. such a way that the obtained azo color image exhibits a uniform color density. It has also been shown that the device which applies the regulated amounts develops u-tréettes for s-fcore stresses, and the developer must be distributed evenly over the image-bearing surface.
En anordning som er forsynt med påforingsvalser, hvilke er spesielt tilpasset for å oppebære en regulert mengde væske samt arbeide i kombinasjon med en gummiskrape eller et annet avstrykningsorgan for ytterligere regulering av væskemengden, har en tendens til å skape sterke friksjonskrefter i fremkalling<g>trinnet. De kraftige friksjonspåkjenningene i fremkallings-trinnet medforer i sin tur en påkjenning på anordningens driv-mekanisme, hvorved drivvalsene bringes i uregelmessig bevegelse. Man får derved en merkbar variasjon i hastigheten. Papiret, A device provided with feed rollers, which are specially adapted to carry a regulated amount of liquid and work in combination with a rubber scraper or other wiping means to further regulate the amount of liquid, tends to create strong frictional forces in the development<g>step . The strong frictional stresses in the developing step in turn cause stress on the device's drive mechanism, whereby the drive rollers are brought into irregular motion. This results in a noticeable variation in speed. the paper,
som skal anvendes ved fremkallingen, fores således gjennom fremkallingsanordningen på feil måte, og dette forårsaker striper og andre uregelmessigheter i kopien på grunn av ujevn væske-påforing. which is to be used in the development, is thus fed through the developing device in the wrong way, and this causes streaks and other irregularities in the copy due to uneven liquid application.
Det er et generelt formål med oppfinnelsen å fremskaffe en forbedret flytende fremkallingskomposisjon for fremkalling av tokomponent-diazotype-materialet, hvilken muliggjor påforing av meget små mengder av nevnte væske slik at denne fordeles jevnt ut over diazotype-materialets overflate. It is a general purpose of the invention to provide an improved liquid developing composition for developing the two-component diazotype material, which enables the application of very small amounts of said liquid so that this is distributed evenly over the surface of the diazotype material.
Et annet formål ifblge oppfinnelsen er å tilveiebringe en forbedret flytende fremkallingskomposisjon for fremkalling av tokomponent-diazotype-materiale, hvilken har evnen til å redusere de påkjenninger som pålegges en fremkallingsanordning under slike betingelser hvorved mindre enn 3 g av nevnte fremkallingsvæske påfores hver m av den overflaten til diazotype-materialet som bærer de latente bildene. Another object according to the invention is to provide an improved liquid developing composition for developing two-component diazo-type material, which has the ability to reduce the stresses imposed on a developing device under such conditions whereby less than 3 g of said developing liquid is applied to each m of that surface to the diazotype material which carries the latent images.
Det er et spesielt formål med oppfinnelsen å tilveiebringe en forbedret fremkallingsvæske-komposisjon for fremkalling av tokomponent-diazotype-materialet ved anvendelse av en konsen-trert losning av et alifatisk amin samt en karboksylholdig fettsyre for å oke systemets smoreevne, og hvorved jevnheten i påforingen i hoy grad understøttes. It is a particular object of the invention to provide an improved developing liquid composition for developing the two-component diazo-type material by using a concentrated solution of an aliphatic amine and a carboxylic fatty acid to increase the smearing ability of the system, and whereby the uniformity of the application in highly supported.
Nevnte formål tilgodeses med en ny fremkallingsvæske-komposisjon, som består av 20 - 80 vekts-% av en aktiv alkalisk komponent, såsom et alifatisk amin, et fortynningsmiddel som består av en flerverdig alkohol, en glykoleter eller en monofunksjonell alkohol, og en karboksylholdig fettsyre med 15-18 karbonatomer i et mengdeforhold på 3-20 vekts-%. Said purpose is met with a new developing liquid composition, which consists of 20 - 80% by weight of an active alkaline component, such as an aliphatic amine, a diluent consisting of a polyhydric alcohol, a glycol ether or a monofunctional alcohol, and a carboxylic fatty acid with 15-18 carbon atoms in a proportion of 3-20% by weight.
Folgende beskrivelse vedrorer nærmere detaljer i forbindelse med spesielt egnede utforelsesformer av fremkalleren ifolge oppfinnelsen. The following description relates to further details in connection with particularly suitable embodiments of the developer according to the invention.
Den alkaliske komponenten i fremkalleren kan være en forbindelse med den generelle formel The alkaline component of the developer may be a compound of the general formula
hvor R^ betyr alkyl, cykloalkyl, alkyl-aryl, alkylol, alkoksy eller alkylolalkoksy, where R 1 means alkyl, cycloalkyl, alkyl-aryl, alkylol, alkoxy or alkylolalkoxy,
R2 og R3 alkyl, cykloalkyl, alkyl-aryl, alkylol, alkoksy, alkylolalkoksy eller hydrogen og hvor R2 and R3 alkyl, cycloalkyl, alkyl-aryl, alkylol, alkoxy, alkylolalkoxy or hydrogen and where
betyr en heterocyklisk ring, såsom morfolin eller piperidin. Egnede og ifolge oppfinnelsen anvendbare aminer er slike med formelen means a heterocyclic ring, such as morpholine or piperidine. Suitable and according to the invention usable amines are those with the formula
hvor R og R' betyr samme eller forskjellige alkyl-eller hydroksyalkyl-grupper eller hydrogen, where R and R' mean the same or different alkyl or hydroxyalkyl groups or hydrogen,
X betyr hydrogen, alkyl eller hydroksyalkyl og hvor n betyr tallet 2, 3 eller 4. X means hydrogen, alkyl or hydroxyalkyl and where n means the number 2, 3 or 4.
Uttrykket "alkylol" er det samme som hydroksyalkyl og"alkylolalkoksy" er det samme som polyol eller hydroksyalkoksyalkyl, hvis uttrykk kan utbyttes mot hverandre. The term "alkylol" is the same as hydroxyalkyl and "alkylolalkoxy" is the same as polyol or hydroxyalkyloxyalkyl, which terms are interchangeable.
Den alkaliske komponenten kan være utspedd méd en forbindelse som er utvalgt fra gruppen bestående av flerverdige alkoholer, en glykoleter, en monofunksjonell alkohol samt vann eller blandinger derav. Fortynningsmidlet foreligger i en mengde på 17 - 60 vekts-%. The alkaline component can be diluted with a compound selected from the group consisting of polyhydric alcohols, a glycol ether, a monofunctional alcohol and water or mixtures thereof. The diluent is present in an amount of 17 - 60% by weight.
Folgende aminer har vist seg å være spesielt egnede ved anvendelse av nærværende fremgangsmåte: monoetanolamin, isopropanol-amin, 2-(2-aminoetoksy)-etanol, trietanolamin, dietanolamin, 2-amino-2-metyl-l-propanol, N-metyletanolamin, dimety1etanolamin, heksylamin og cykloheksylamin. Også andre aminer har evnen The following amines have been found to be particularly suitable when using the present method: monoethanolamine, isopropanolamine, 2-(2-aminoethoxy)ethanol, triethanolamine, diethanolamine, 2-amino-2-methyl-1-propanol, N-methylethanolamine , dimethylethanolamine, hexylamine and cyclohexylamine. Other amines also have the ability
til å kunne fremkalle diazo-kopi, såsom P-hydroksyetyltrimetyl-ammoniumkarbonat, N-aminoetyletanolamin, alkyl-substituert morfolin og piperidin, men disse sistnevnte er mindre egnet på grunn av at de har en merkbar lukt, eller på grunn av at de har en tendens til å påvirke fargenyansene i skadelig retning. to be able to induce diazo copy, such as P-hydroxyethyltrimethylammonium carbonate, N-aminoethylethanolamine, alkyl-substituted morpholine and piperidine, but these latter are less suitable because they have a noticeable smell, or because they have a tendency to affect the color shades in a harmful direction.
Anvendelsen av et fortynningsmiddel fremmer spredningen eller fordelingen av fremkalleren over den påfbrte overflaten og dermed dennes fukting. Fortynningsmidlet kan også anvendes for innstilling av fremkallingsvæskens viskositet, slik at denne lett kan bringes til å flyte gjennom forskjellige ledninger og frem til iiremkallingssonen. Hvis fortynningsmidlet dessuten oppviser ho<y>ere -flyktighet enn det alifatiske aminet, så har det evnen til å avdunste fra overflaten med en torkende effekt på det tynne sjiktet. The use of a diluent promotes the spreading or distribution of the developer over the applied surface and thus its wetting. The diluent can also be used to adjust the viscosity of the developing liquid, so that it can easily be made to flow through various lines and up to the iiremkalling zone. If the diluent also exhibits higher volatility than the aliphatic amine, then it has the ability to evaporate from the surface with a drying effect on the thin layer.
Fortynningsmidlet kan består av en flerverdig alkohol, såsom heksylenglykol, dietylenglykol, polyetylenglykol, trimetylen-glykol, etylenglykol, propylenglykol, dipropylenglykol, glycerol og glykol-etre, såsom etylenglykolmonoetyleter (Cellosolve), dietylenglykolmonoetyleter, dietylenglykolmonometyleter, butyl-Cellosolve, eller en monofunksjonell alkohol, såsom 4-metoksy-4-metyl-pentanol-2 (Pentoksyl), 2-etylheksanol, cykloheksanol, isooktylalkohol og heksanol. The diluent may consist of a polyhydric alcohol, such as hexylene glycol, diethylene glycol, polyethylene glycol, trimethylene glycol, ethylene glycol, propylene glycol, dipropylene glycol, glycerol and glycol ethers, such as ethylene glycol monoethyl ether (Cellosolve), diethylene glycol monoethyl ether, diethylene glycol monomethyl ether, butyl Cellosolve, or a monofunctional alcohol, such as 4-methoxy-4-methyl-pentanol-2 (Pentoxyl), 2-ethylhexanol, cyclohexanol, isooctyl alcohol and hexanol.
Det har vist seg å være fordelaktig å anvende slike flerverdige • alkoholer som er fullstendig kombinerbare med de alifatiske aminene, og som ikke skadelig påvirker kopiens kvalitet. Videre fremmer flerverdige alkoholer, såsom heksylenglykol, og glykol-tre, spredningen av fremkallingsvæsken. It has proven to be advantageous to use such polyhydric • alcohols which are completely combinable with the aliphatic amines, and which do not adversely affect the quality of the copy. Furthermore, polyhydric alcohols, such as hexylene glycol and glycol wood, promote the spreading of the developing liquid.
Det med oppfinnelsen erholdte tekniske fremskritt representeres av tilsetningen av en tredje komponent, såsom en karboksylisk fettsyre med en karbonkjedelengde på 16 - 18 karbonatomer, såsom stearinsyre, palmitinsyre, cis-9-octadecensyre, cis,cis-9,12-oktadekadiensyre eller cis,cis,cis-9,12,15-oktadekatriensyre, The technical progress obtained with the invention is represented by the addition of a third component, such as a carboxylic fatty acid with a carbon chain length of 16 - 18 carbon atoms, such as stearic acid, palmitic acid, cis-9-octadecenoic acid, cis,cis-9,12-octadecadienoic acid or cis, cis,cis-9,12,15-octadecatrienoic acid,
i et mengdeforhold på 3 - 20 vekts-%. in a quantity ratio of 3 - 20% by weight.
Man bør legge merke til at den mengde karboksylsyre, One should notice that the amount of carboxylic acid,
som skal tilsettes fremkallingskomposisjoner for reduksjon av friksjonskreftene i fremkallings-systemet, kan være avhengig av konsentrasjonen av organisk amin. Det har vist seg at det ved de hoyere konsentrasjonene kan være nodvendig å oppvarme fremkalleren til en temperatur over romtemperatur for å holde karbok-syl syr ekomponent en i losning. which must be added to developing compositions to reduce the frictional forces in the developing system, may depend on the concentration of organic amine. It has been shown that at the higher concentrations it may be necessary to heat the developer to a temperature above room temperature in order to keep the carboxylic acid component in solution.
Oppfinnelsen anskueliggjøres nærmere ved hjelp av folgende eksempler, hvorved forekommende prosenttall henforer seg til vekten, når ikke annet angis. Man bor legge merke til at kombinasjonen av "fet alkanolamin med en karboksylisk fettsyre gir alkanolaminsaltet. Således gir f.eks. stearinsyre stearat-saltet av monoetanolamin. The invention is illustrated in more detail by means of the following examples, whereby occurring percentages refer to the weight, when not stated otherwise. It should be noted that the combination of "fatty alkanolamine with a carboxylic fatty acid gives the alkanolamine salt. Thus, for example, stearic acid gives the stearate salt of monoethanolamine.
EKSEMPEL 1 EXAMPLE 1
Komponentene blandes i et blandingskar, inntil man får en enhetlig losning. Losningen tilfores fremkallerdelen i en frernkallingsanordning, og som er beskrevet i den samtidig um behandling værende amerikanske patentansokning nr. 831.685. The components are mixed in a mixing vessel until a uniform solution is obtained. The solution is supplied to the developer part in a remote development device, and which is described in the simultaneously pending US patent application No. 831,685.
EKSEMPEL 2 EXAMPLE 2
EKSEMPEL 3 EKSEMPEL 4 EXAMPLE 3 EXAMPLE 4
EKSEMPEL 5 EXAMPLE 5
EKSEMPEL 6 EKSEMPEL 7 EKSEMPEL 8 EKSEMPEL 9 EXAMPLE 6 EXAMPLE 7 EXAMPLE 8 EXAMPLE 9
' " Kr»/ "Kr"/
EKSEMPEL IO EXAMPLE IO
EKSEMPEL 11 EXAMPLE 11
EKSEMPEL 12 EXAMPLE 12
EKSEMPEL 13 EXAMPLE 13
I hver og en av de oven beskrevne fremkallingslosningene In each of the developing solutions described above
medfbrte tilsetning av den karboksyliske fettsyren den nød- entailed the addition of the carboxylic fatty acid that
vendige smbre-egenskapen, hvorved man i den anvendte fremkallings- reversible smbre property, whereby in the used developing
anordningen kunne tilveiebringe en enhetlig fordeling av væsken over den for fremkallingen anvendte overflaten i et mengde- the device could provide a uniform distribution of the liquid over the surface used for development in a quantity
forhold på 0,5 - 3 g pr. m 2 og dette uten at drivmekanismen blir gjenstand for noen skadelig påkjenning, fremføringen av kopibanen gjennom fremkallings-stasjonen var jevn og sikker, ratio of 0.5 - 3 g per m 2 and this without the drive mechanism being subjected to any harmful stress, the advancement of the copy web through the developing station was smooth and safe,
og man kunne ikke merke noen slik rykking eller annen uregel- and one could not notice any such twitching or other irregularity-
messig bevegelse som kan iakttas ved anvendelse av fremkallings- relative movement that can be observed when using developing
væsker som ikke inneholder karboksyliske fettsyrer, hvorved striper og ujevn azofarge-dannelse på baneoverflaten fås. liquids that do not contain carboxylic fatty acids, whereby streaks and uneven azo dye formation on the web surface are obtained.
Claims (2)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12854171A | 1971-03-26 | 1971-03-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO138049B true NO138049B (en) | 1978-03-06 |
| NO138049C NO138049C (en) | 1978-06-14 |
Family
ID=22435825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO987/72A NO138049C (en) | 1971-03-26 | 1972-03-23 | PROCEDURES FOR DIAZOCOPICATION USING SMALL QUANTITATIVE PRODUCTS AND AMINIDE DEVELOPMENTS FOR SUCH USE |
Country Status (22)
| Country | Link |
|---|---|
| JP (1) | JPS503942B1 (en) |
| AR (1) | AR192627A1 (en) |
| AT (1) | AT315637B (en) |
| AU (1) | AU458945B2 (en) |
| BE (1) | BE781294A (en) |
| BR (1) | BR7201726D0 (en) |
| CA (1) | CA982391A (en) |
| CH (1) | CH581848A5 (en) |
| CS (1) | CS196450B2 (en) |
| DK (1) | DK140736B (en) |
| ES (1) | ES401173A1 (en) |
| FI (1) | FI54978C (en) |
| FR (1) | FR2130679B1 (en) |
| GB (1) | GB1373250A (en) |
| HU (1) | HU166961B (en) |
| IT (1) | IT950491B (en) |
| NL (1) | NL157996B (en) |
| NO (1) | NO138049C (en) |
| SE (1) | SE380106B (en) |
| TR (1) | TR18542A (en) |
| YU (1) | YU34464B (en) |
| ZA (1) | ZA721881B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL168344C (en) * | 1976-12-10 | 1982-03-16 | Oce Van Der Grinten Nv | METHOD FOR PREPARING A DEVELOPMENT FLUID FOR DIAZOTYPIC MATERIAL AND METHOD FOR MAKING A COPY WITH SUCH A DEVELOPER |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1518043A (en) * | 1966-02-15 | 1968-03-22 | Hall Harding Ltd | Improvements relating to the development of diazotypic materials |
-
1971
- 1971-11-16 CA CA127,812A patent/CA982391A/en not_active Expired
- 1971-11-18 GB GB5368471A patent/GB1373250A/en not_active Expired
- 1971-12-13 AU AU36806/71A patent/AU458945B2/en not_active Expired
-
1972
- 1972-03-20 ZA ZA721881A patent/ZA721881B/en unknown
- 1972-03-22 JP JP47028194A patent/JPS503942B1/ja active Pending
- 1972-03-22 DK DK134072AA patent/DK140736B/en not_active IP Right Cessation
- 1972-03-22 IT IT22248/72A patent/IT950491B/en active
- 1972-03-23 CH CH434872A patent/CH581848A5/xx not_active IP Right Cessation
- 1972-03-23 NO NO987/72A patent/NO138049C/en unknown
- 1972-03-24 NL NL7203991.A patent/NL157996B/en not_active IP Right Cessation
- 1972-03-24 AR AR241155A patent/AR192627A1/en active
- 1972-03-24 BR BR721726A patent/BR7201726D0/en unknown
- 1972-03-24 SE SE7203912A patent/SE380106B/xx unknown
- 1972-03-24 FR FR7210453A patent/FR2130679B1/fr not_active Expired
- 1972-03-24 FI FI835/72A patent/FI54978C/en active
- 1972-03-24 YU YU785/72A patent/YU34464B/en unknown
- 1972-03-24 AT AT259072A patent/AT315637B/en not_active IP Right Cessation
- 1972-03-25 HU HUAE357A patent/HU166961B/hu unknown
- 1972-03-25 ES ES401173A patent/ES401173A1/en not_active Expired
- 1972-03-27 BE BE781294A patent/BE781294A/en not_active IP Right Cessation
- 1972-03-27 TR TR18542A patent/TR18542A/en unknown
- 1972-03-27 CS CS722024A patent/CS196450B2/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE781294A (en) | 1972-07-17 |
| NO138049C (en) | 1978-06-14 |
| ES401173A1 (en) | 1975-02-01 |
| DK140736B (en) | 1979-11-05 |
| SE380106B (en) | 1975-10-27 |
| YU34464B (en) | 1979-07-10 |
| FI54978C (en) | 1979-04-10 |
| AT315637B (en) | 1974-06-10 |
| AU3680671A (en) | 1973-06-14 |
| DE2214475B2 (en) | 1974-10-10 |
| AU458945B2 (en) | 1975-03-13 |
| CA982391A (en) | 1976-01-27 |
| NL7203991A (en) | 1972-09-28 |
| HU166961B (en) | 1975-07-28 |
| GB1373250A (en) | 1974-11-06 |
| AR192627A1 (en) | 1973-02-28 |
| DE2214475A1 (en) | 1972-11-23 |
| IT950491B (en) | 1973-06-20 |
| FR2130679B1 (en) | 1976-06-11 |
| DK140736C (en) | 1980-03-24 |
| FI54978B (en) | 1978-12-29 |
| JPS503942B1 (en) | 1975-02-12 |
| FR2130679A1 (en) | 1972-11-03 |
| TR18542A (en) | 1977-03-16 |
| ZA721881B (en) | 1972-12-27 |
| CH581848A5 (en) | 1976-11-15 |
| CS196450B2 (en) | 1980-03-31 |
| NL157996B (en) | 1978-09-15 |
| YU78572A (en) | 1978-12-31 |
| BR7201726D0 (en) | 1973-05-31 |
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