US2773768A - Light-sensitive diazotype material - Google Patents
Light-sensitive diazotype material Download PDFInfo
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- US2773768A US2773768A US276062A US27606252A US2773768A US 2773768 A US2773768 A US 2773768A US 276062 A US276062 A US 276062A US 27606252 A US27606252 A US 27606252A US 2773768 A US2773768 A US 2773768A
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- diazo
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- 239000000463 material Substances 0.000 title claims description 59
- -1 DIAZO Chemical class 0.000 claims description 19
- 239000007787 solid Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 126
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 67
- 150000008049 diazo compounds Chemical class 0.000 description 35
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 125000004432 carbon atom Chemical group C* 0.000 description 18
- 229920002678 cellulose Polymers 0.000 description 15
- 229920002301 cellulose acetate Polymers 0.000 description 14
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- 150000001450 anions Chemical group 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 12
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 11
- 125000002252 acyl group Chemical group 0.000 description 10
- 230000002209 hydrophobic effect Effects 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 235000005074 zinc chloride Nutrition 0.000 description 7
- 239000011592 zinc chloride Substances 0.000 description 7
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 238000005266 casting Methods 0.000 description 4
- 230000008878 coupling Effects 0.000 description 4
- 238000010168 coupling process Methods 0.000 description 4
- 238000005859 coupling reaction Methods 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- HXXFHGQTUYFAND-UHFFFAOYSA-N 4-diazo-N,N-dihexylcyclohexa-1,5-dien-1-amine Chemical compound [N+](=[N-])=C1CC=C(N(CCCCCC)CCCCCC)C=C1 HXXFHGQTUYFAND-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 3
- 229960001553 phloroglucinol Drugs 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 229920000298 Cellophane Polymers 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000006149 azo coupling reaction Methods 0.000 description 2
- 230000036461 convulsion Effects 0.000 description 2
- 230000020176 deacylation Effects 0.000 description 2
- 238000005947 deacylation reaction Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- IEAIRBBRIGJNDN-UHFFFAOYSA-N 4-diazo-N,N-bis(3-methylbutyl)cyclohexa-1,5-dien-1-amine Chemical compound [N+](=[N-])=C1CC=C(N(CCC(C)C)CCC(C)C)C=C1 IEAIRBBRIGJNDN-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920002160 Celluloid Polymers 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- TUCNEACPLKLKNU-UHFFFAOYSA-N acetyl Chemical compound C[C]=O TUCNEACPLKLKNU-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229920013820 alkyl cellulose Polymers 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 229910001864 baryta Inorganic materials 0.000 description 1
- STOFQWNQZIPXAW-UHFFFAOYSA-N benzene-1,3-diol;benzene-1,3,5-triol Chemical compound OC1=CC=CC(O)=C1.OC1=CC(O)=CC(O)=C1 STOFQWNQZIPXAW-UHFFFAOYSA-N 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- YXVFQADLFFNVDS-UHFFFAOYSA-N diammonium citrate Chemical compound [NH4+].[NH4+].[O-]C(=O)CC(O)(C(=O)O)CC([O-])=O YXVFQADLFFNVDS-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- VKDSBABHIXQFKH-UHFFFAOYSA-M potassium;4-hydroxy-3-sulfophenolate Chemical compound [K+].OC1=CC=C(O)C(S([O-])(=O)=O)=C1 VKDSBABHIXQFKH-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- AZXQLMRILCCVDW-UHFFFAOYSA-M sodium;5-propan-2-ylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(C(C)C)=CC=CC2=C1S([O-])(=O)=O AZXQLMRILCCVDW-UHFFFAOYSA-M 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 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
- G03C1/00—Photosensitive materials
- G03C1/52—Compositions containing diazo compounds as photosensitive substances
- G03C1/54—Diazonium salts or diazo anhydrides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
Definitions
- the invention relates to lightsensitivc diazotypc material and particularly to diazotype material comprising a support bearing a diazo film layer of the so-called one-component type which is suitable for development with a thin layer of an aqueous developer.
- material of the one-component type is meant the type in which the diazo film layer contains a diazo component but no coupling component.
- diazo-film layer a special type of diazo layer.
- the generic term diazo layer is also used when the diazo compound is simply spread out on the fibres of a paper surface as a dried-up coating, perhaps in the form of a very thin. uneven, and possibly discontinuous diazo surface.
- a diazo film layer in accordance with the present invention has the character of a true layer of measurable thickness.
- a diazo film layer need not be of uniform thickness through out; it may for example, show a relief.
- Such a diazo film layer comprises material which will be referred to hereinafter as film-forming material.”
- the demarcation between the support and the diazo film layer may be sharp, as is generally the case with a layer cast on to a support.
- a sharp demarcation may, however, be absent, as is the case, for example, when a cellulose ester film is superficially saponified and the diazo compound is absorbed into the saponified surface.
- the unsaponified part is considered as the support and the saponified part constitutes the film layer; the acyl content of the latter increases from the outside to the inside.
- the diazo film layers are clearly distinguished from diazo layers of the type described above even though there be no sharp demarcation between the diazo film layer and the support.
- Light-sensitive diazotype materials with a diazo film layer are known. Mention may be made of cellulose acetate films with a deacylated surface, impregnated with a diazo compound without any azo coupling component, and of the diazo film layers with an 2120 coupling component described in British specification No. 563,804. Diazolype material containing a diazo film layer including an azo coupling component. the film-forming material of which consists of gclatine, has also been produced. Photographic material with a lighbsensitive layer of cellulose acetate with a low acetyl content has been described in British specification No. 496,049.
- This specification chiefly relates to material in which the light-sensitive substance is a silver halide, but reference is also made to colouring processes based on the use of diazo compounds without any further information being given.
- Other types of diazo film layers are described in British specifications Nos. 311,196, 318,511 and 563,547.
- the known diazotype materials with a diazo film layer or the one-component type are developed by the application of a thin layer of aqueous developing liquid.
- the developer usually contains phloroglucinol, a very active coupling compound, which may couple with the diazo compound in one. two or three positions and produce dyes in various shades accordingly.
- Use may also be made of a mixture of phloroglucinol with other coupling components, for example rciorcinol, with a view to producing good neutral shades.
- the diazo film layers need to be resistant to treatment with the thin layer of aqueous developer, i. e. the filmforming material employed must not present any serious difificulty when treated with an aqeous liquid. for example by reason of melting, dissolving, or becoming objuc tionably sticky, as is the case with layers of. gum, alkyl cellulose, soft gelatine and similar substances. On the other hand it must be capable of readily accepting and absorbing the thin layer of developer.
- Suitable film layers are, for example, cellulose (cellulose hydrate of cellophane) films and the like, and in particular layers of cellulose esters of such an acyl content that they can absorb the aqueous developer.
- Other suitable layers are those of polyvinyl esters with such an acyl content. Such layers can very readily be obtained by deacylation of layers with a higher ucyl content. in the case of the cellulose ester layers tleacylation may be very extensive or even complete.
- the diazo film layers must contain large quantities of the diazo compounds per unit of surface area. If this quantity is expressed in millimols of diazo compound per sq. metre. it may be stated that the ordinary diazotype papers contain about 0.3 to 0.5, and the modern diaaotypc material with diazo film layers generally more (sometimes up to 1.0 and even 1.5 millimols) diazo compound per sq. metre. These diazo film layers are particularly sensitive to developing fluctuations.
- the sensitivity of diazo film layers to developing Eluctuutions shews itself in variations of the shades in the colours of the image, for example in deviations from the desired neutral black. Jerks and vibrations in the developing equipment are thus noticeable in the copies, particularly if large dark areas are present in the image, as streaks with alternate shades of, for example, green-black and violet-black.
- lightseusitivc d1 axoiype material containing a support bearing a diazo tiim layer of the so-called one component type which is suitable for development with a ⁇ hill layer of a developer contains in the diazo film layer a diazo compound of the general formula:
- R1 and R2 are alkyl radicals having together 10. ll or 12 carbon atoms. each nlkyl radical containing at least four and at most seven carbon atoms. and not more than one of the two having a side chain attached to the alpha carbon atom.
- light-sensitive diazotype materials of this composition are less sensitive to developing fluctuations than those containing in the diazo film layer other diazo com pounds that are suitable per se for such development, for example the well-known, frequently applied, and otherwise eminently suitable paradiazo-ethyl-benzyl-aniline.
- the light-sensitive diazo film layers according to the invention may contain the admixture generally used in diazotype printing, such as acids, stabilisers, anti-disco]- ouration agents, and the like.
- the diazo film layer may be cast on to the support, the casting material already containing the diazo compound. In employing the casting process. however it is preferable to cast the film layer. allow it to set and dry, and then impregnate it with a solution of the diazo compound. It is also possible to cast the film layer on to another support, for example a cylinder surface, and transfer it after drying to the desired support, again with the diazo compound already present in the casting material or with subsequent impregnation.
- Such film layers can be obtained in the manner described above by casting, with or without a subsequent impregnation, but also by partial deacylation of the surface of a foil or film of cellulose acetate with a higher acetyl content.
- the acetyl content in the film layer formed is not the same throughout; in a cross-see lion through the support with the film layer it will stead ily increase from the outside of the said layer inwards.
- the basis taken is the average found in the part of the film layer that does not dissolve in dry acetone.
- the film layer mounted on a hydrophobic sublayer. This may be formed separately. With superficially deacylated cellulose acetate layers it will already be present, since the original cellulose acetate is hydrophobic owing to its high acetyl content.
- the cellulose acetates may also contain other acyl radicals besides the acetyl radical.
- Suitable supports for the diazo film layer are, for ex ample, paper, baryta-coated paper, transparent paper, linen, Celluloid film, cellulose acetate film, plastic supports, metal sheets and glass.
- the materials according to the invention are propcrly made, they can be used for making copies w ich have to meet high demands as to the strength of the image and the uniformity of shade, for example for copying originals of artistic value, photographic diapositives, cinematographic films, and the like.
- Example I Paper of weight 150 g. per sq. metre, coated on one side with a cellulose acetate (about 50% by weight of combined acetic acid) layer of about my. thickness. which has been applied on the paper by means of an adhesive and which is deacylated to a depth of about 4 me to an average acetyl content. calculated as combined acetic acid, of about by weight (which corresponds to an average number of acetyl groups attached to the OH groups of 0.7) is sensitized by impregnation for seconds on the deacetylated side of the cellulose acetate layer with the following solution:
- Example I A paper with a film layer as described in llxample l is sensitised in the same way with a solution of:
- the diazo film layer thus formed is located on a hydrophobic sublayer, as in Example 1.
- the material After exposure under a tracing with insufiicient ligh for complete exposure, the material is developed in a developing equipment of the kind described in British P. S. 656,674 at a rate of 5 metres per minute, 8.5 g. per sq. metre of the developer according to Example I being applied at normal strength. A strong black image on a good grey background is obtained.
- Example III A paper with a film layer as described in Example I is sensitised in the same manner with a solution of:
- the diazo film layer described above is located on a hydrophobic sublayer.
- the material After exposure under a diapositive, the material is developed at a rate of 1.50 metres per minute, 7 g. per sq. metre of the developer according to Example I being applied.
- a strong black image is obtained in which, even when large areas of medium tone are present, few if any deviations in shade resulting from vibrations and mechanical inequalities of the developing. equipment are to be noticed.
- 24 parts of p-diazo-di-isoarnylaniline-ZnClz salt 23 parts of p-diazo-ethyl-benzylaniline- ZnCLz salt are employed, large areas of medium tone in the image shew, as a result of inequalities in the developing equipment, variously coloured streaks.
- Example IV A cellulose acetobutyrate film of 100 mu thickness with an average a-cyl content of 31% by weight of acetyl and 17% by weight of butyryl is superficially hydrolysed on one side by dipping in a solution of: 0.35 nKOH in methylalcohol (50%) for seconds at C.
- the excess liquid is removed from the cellulose ester surface, and the material is then dried.
- the diazo film layer then contains about 0.8 millimol of diazo compound per sq. metre, and is located on a hydrophobic sublayer.
- the material is developed with a phloroglucinol-resorcinol developer according to Example I, about 9 g. per sq. metre being applied. A black image with uniform shade in all the areas is obtained. Copies of this type are very suitable for projection purposes.
- Example V On paper coated with a hydrophobic layer of cellulose acetate (with an acetyl content, calculated as combined acetic acid, of about 53% by weight of acetic acid) of a thickness of about 10 m a layer of 90 g. per sq. metre of the following liquid is applied by dipping at 20 C.
- Example VI A cellulose film (cellulose hydrate foil, cellophane) with a thickness of 25 m is applied on paper by means of adhesive. The film is then sensitised with the following solution:
- the diazo film layer then contains about 0.4 g. of diazo compound per sq. metre, which corresponds to about 0.8 millimol per sq. metre.
- the mate rial After exposure under a transparent original, the mate rial is developed by the application of about 9 g. per sq. metre of the developing solution described in Example l. A strong black image is obtained, which shows little variation in shade as a result of developing fluctuations.
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo lm layer is a continuous substantially dry and non-sticky layer of measurable thickness that covers said support, contains an organic colloidal solid film-forming material, is hydrophilic and contains substantially entirely within said layer a diazo compound of the general formula:
- R1 and R2 are alkyl radicals together having a total of from 10 to 12 carbon atoms, each alkyl radical containing at least 4 and at most 7 carbon atoms, and not more than one of the two having a side chain attached to the alpha carbon atom.
- Light-sensitive diazotype material according to claim 1, wherein the film-forming material of the diazo film layer consists essentially of hydrolysed cellulose acetate with an average acetyl content, expressed as combined acetic acid, of 0% by weight to 35% by weight.
- Light-sensitive diazotype material according to claim 1 wherein a hydrophobic interlayer is present between the support and the diazo film layer.
- Light-sensitive diazotype material which comprises a support of cellulose ester film saponified at least on the surface to at most a low acyl content and having said diazo compound absorbed in said saponified surface.
- Light-sensitive diazotype material according to claim 5 wherein the cellulose ester film is itself carried by a paper support.
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous layer of measurable thickness that covers said support, contains as a film-forming material regenerated cellulose.
- R1 and R2 are alkyl radicals together having a total of from 10 to 12 carbon atoms, each alkyl radical containing at least four and at most seven carbon atoms, and not more than one of the two having a side chain attached to the alpha carbon atom.
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous layer of measurable thickness that covers said support, contains as a film-forming material cellulose acetobutyrate saponified to at most a low acyl content at its surface, is hydrophilic, and has absorbed therein a diazo compound of the general formula:
- R1 and R2 are alkyl radicals together having a total of from 10 to 12 carbon atoms, each alkyl radical containing at least four and at most seven carbon atoms, and not more than one of the two having a side chain attached to the alpha carbon atom.
- Light-sensitive diazotype material comprising a sup port bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous layer of measurable thickness that covers said support, contains as a film-forming material polyvinyl acetate saponified to at most a low acyl content at its surface, is hydrophilic, and has absorbed therein a diazo compound of the general formula:
- R1 and R2 are alkyl radicals together having a total of from 10 to 12 carbon atoms, each alkyl radical containing at least four and at most seven carbon atoms, and not more than one of the two having a side chain atached to the alpha carbon atom.
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous substantially dry and non-sticky layer of measurable thickness that causes said support, contains an organic colloidal solid film forming material is hydrophilic, and contains substantially entirely within said layer a diazo compound of the general formula:
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous layer of measurable thickness that covers said support consists essentially of a cellulose ester film saponified to at most a low acyl content at its surface, is hydrophilic, and has absorbed therein a salt of p-diazo-di-n-hexyl aniline.
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuone substantially dry and non-sticky layer of measurable thickness that covers said support, contains an organic colloidal solid film forming material, is hydrophilic, and contains absorbed therein a diazo compound of the general formula:
- X is an anion and R1 is a secondary amyl radical and R2 is an n-hexyl radical.
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous stubstantially dry and non-sticky layer of measurable thickness that covers said support, contains an organic colloidal solid film forming material, is hydrophilic, and contains absorbed therein a diazo compound of the general formula:
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous substantially dry and non-sticky layer of measurable thickness that covers said support, contains an organic colloidal solid film forming material, is hydrophilic, and contains absorbed therein a diazo compound of the general formula:
- X is an anion and R1 is an n-hexyl radical and R2 is an namyl radical.
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous layer of measurable thickness that covers said support, consists essentially of a cellulose ester film saponified to at most a low acyl content at its surface, is hydrophilic, and contains absorbed therein a diazo compound of the general formula:
- X is an anion and R1 and R: are each n-amyl radicals.
- Light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aqueous developer, wherein the diazo film layer is a continuous layer of measurable thickness that covers said support, consists essentially of a cellulose ester film saponified to at most a low acyl content at its surface, is hydrophilic, and contains absorbed therein a diazo compound of the general formula:
- a light-sensitive diazotype material comprising a support bearing a one-component diazo film layer which is suitable for development with a thin layer of an aque ous developer, wherein the diazo film layer is a continuous substantially dry and non-sticky layer of measurable thickness that covers said support, contains an organic colloidal solid film-forming material, is hydrophilic, and contains substantially entirely within said layer more than 0.5 millimol per square meter of a diazo compound of the general formula:
- R1 and R2 are alkyl radicals together having a total of from 10 to 12 carbon atoms, each alkyl radical containing at least four and at most seven carbon atoms, and not more than one of the two having a side chain attached to the alpha carbon atom.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL159955 | 1951-03-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2773768A true US2773768A (en) | 1956-12-11 |
Family
ID=19750515
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US276062A Expired - Lifetime US2773768A (en) | 1951-03-20 | 1952-03-11 | Light-sensitive diazotype material |
Country Status (7)
Country | Link |
---|---|
US (1) | US2773768A (en(2012)) |
CH (1) | CH307021A (en(2012)) |
DE (1) | DE973598C (en(2012)) |
ES (1) | ES202557A1 (en(2012)) |
FR (1) | FR1058926A (en(2012)) |
GB (2) | GB711390A (en(2012)) |
NL (1) | NL82334C (en(2012)) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3052542A (en) * | 1958-07-24 | 1962-09-04 | Gen Aniline & Film Corp | Intermediate master for use in the diazotype process and a process for producing same |
US3320061A (en) * | 1963-06-24 | 1967-05-16 | Xerox Corp | Masking by total internal reflection for image reproduction and display |
US3389996A (en) * | 1964-10-15 | 1968-06-25 | Gen Aniline & Film Corp | Two-component heat developable diazotypes |
US3650750A (en) * | 1968-12-28 | 1972-03-21 | Ricoh Kk | Heat-developable diazo-type light-sensitive material |
US4043816A (en) * | 1972-05-26 | 1977-08-23 | Oce-Van Der Grinten N.V. | Photographic process for making diazotype copies utilizing small quantity of liquid developer |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1693196B2 (de) * | 1965-05-08 | 1976-03-04 | Hoechst Ag, 6000 Frankfurt | Einkomponenten-diazotypiematerial |
US3622325A (en) * | 1968-03-07 | 1971-11-23 | Ricoh Kk | Diazotype photographic copying material adapted for wet development and for producing copied image in black color |
NL176020C (nl) * | 1974-09-13 | 1985-02-01 | Oce Van Der Grinten Nv | Werkwijze voor het vervaardigen van diazotypkopieen, alsmede diazotypmateriaal voor het uitvoeren van deze werkwijze. |
FR2300354A1 (fr) * | 1975-02-04 | 1976-09-03 | Kodak Pathe | Plaque presensibilisee comprenant u |
US4306007A (en) * | 1978-03-13 | 1981-12-15 | Am International, Inc. | Process of making and using fade-resistant diazo microfilm |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1756400A (en) * | 1926-02-22 | 1930-04-29 | Kalle & Co Ag | Light-sensitive materials and process of making them |
GB332552A (en) * | 1929-02-22 | 1930-07-21 | Frans Van Der Grinten | Improvements in or relating to the preparation of photographic diazotypes |
GB337868A (en) * | 1929-08-24 | 1930-11-13 | Humphrey Desmond Murray | Improvements in and relating to the manufacture of sensitized bases for photographic purposes |
US1821281A (en) * | 1926-12-11 | 1931-09-01 | Frans Van Der Grinten | Manufacture of diazo-types |
US1841653A (en) * | 1927-08-22 | 1932-01-19 | Frans Van Der Grinten | Process for developing positive diazo prints |
US1967371A (en) * | 1931-03-28 | 1934-07-24 | Kalle & Co Ag | Process of preparing copies |
GB425235A (en) * | 1933-09-11 | 1935-03-11 | Werner Paul Leuch | Improvements in or relating to the production of photographic diazotype prints |
US2066918A (en) * | 1931-09-21 | 1937-01-05 | Light-sensitive material and a proc | |
US2067690A (en) * | 1930-02-05 | 1937-01-12 | Philips Nv | Method and material for obtaining photographic contrasts |
US2209087A (en) * | 1933-10-27 | 1940-07-23 | Dietzgen Eugene Co | Production of photographic diazotype prints |
US2311016A (en) * | 1934-01-19 | 1943-02-16 | Hartford Nat Bank & Trust Co | Photographic material and method of producing same |
US2336309A (en) * | 1941-05-29 | 1943-12-07 | Eastman Kodak Co | Diazotype photographic material |
US2532126A (en) * | 1946-12-16 | 1950-11-28 | Gen Aniline & Film Corp | Diazotype photographic material |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL28421C (en(2012)) * | 1926-12-11 | |||
NL20192C (en(2012)) * | 1927-02-10 | |||
CH191032A (de) * | 1935-08-23 | 1937-05-31 | Naamlooze Vennootschap Chemisc | Verfahren zum Kopieren auf positiven Diazotypschichten. |
DE725305C (de) * | 1939-04-14 | 1942-09-18 | Grinten Chem L V D | Verfahren zur Herstellung von Rasterreflexkopien |
US2532744A (en) * | 1945-07-04 | 1950-12-05 | Gen Aniline & Film Corp | Diazotype containing as the azo component a quaternary salt of 2-methyl-6-methoxy-benzoselenazole |
US2501874A (en) * | 1946-06-12 | 1950-03-28 | Gen Aniline & Film Corp | Photographic diazo-sensitized glassine paper |
US2496240A (en) * | 1947-06-06 | 1950-01-31 | Gen Aniline & Film Corp | Diazotypes stabilized with sulfo amino benzoic acids |
DE905452C (de) * | 1947-12-17 | 1954-01-14 | Gen Aniline & Film Corp | Diazotypieverfahren |
-
0
- NL NL82334D patent/NL82334C/xx active
-
1952
- 1952-01-17 GB GB1372/52A patent/GB711390A/en not_active Expired
- 1952-02-20 GB GB4502/52A patent/GB698027A/en not_active Expired
- 1952-03-11 US US276062A patent/US2773768A/en not_active Expired - Lifetime
- 1952-03-19 FR FR1058926D patent/FR1058926A/fr not_active Expired
- 1952-03-19 CH CH307021D patent/CH307021A/de unknown
- 1952-03-20 ES ES0202557A patent/ES202557A1/es not_active Expired
- 1952-03-20 DE DEG8437A patent/DE973598C/de not_active Expired
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1756400A (en) * | 1926-02-22 | 1930-04-29 | Kalle & Co Ag | Light-sensitive materials and process of making them |
US1821281A (en) * | 1926-12-11 | 1931-09-01 | Frans Van Der Grinten | Manufacture of diazo-types |
US1841653A (en) * | 1927-08-22 | 1932-01-19 | Frans Van Der Grinten | Process for developing positive diazo prints |
GB332552A (en) * | 1929-02-22 | 1930-07-21 | Frans Van Der Grinten | Improvements in or relating to the preparation of photographic diazotypes |
GB337868A (en) * | 1929-08-24 | 1930-11-13 | Humphrey Desmond Murray | Improvements in and relating to the manufacture of sensitized bases for photographic purposes |
US2067690A (en) * | 1930-02-05 | 1937-01-12 | Philips Nv | Method and material for obtaining photographic contrasts |
US1967371A (en) * | 1931-03-28 | 1934-07-24 | Kalle & Co Ag | Process of preparing copies |
US2066918A (en) * | 1931-09-21 | 1937-01-05 | Light-sensitive material and a proc | |
GB425235A (en) * | 1933-09-11 | 1935-03-11 | Werner Paul Leuch | Improvements in or relating to the production of photographic diazotype prints |
US2209087A (en) * | 1933-10-27 | 1940-07-23 | Dietzgen Eugene Co | Production of photographic diazotype prints |
US2311016A (en) * | 1934-01-19 | 1943-02-16 | Hartford Nat Bank & Trust Co | Photographic material and method of producing same |
US2336309A (en) * | 1941-05-29 | 1943-12-07 | Eastman Kodak Co | Diazotype photographic material |
US2532126A (en) * | 1946-12-16 | 1950-11-28 | Gen Aniline & Film Corp | Diazotype photographic material |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3052542A (en) * | 1958-07-24 | 1962-09-04 | Gen Aniline & Film Corp | Intermediate master for use in the diazotype process and a process for producing same |
US3320061A (en) * | 1963-06-24 | 1967-05-16 | Xerox Corp | Masking by total internal reflection for image reproduction and display |
US3389996A (en) * | 1964-10-15 | 1968-06-25 | Gen Aniline & Film Corp | Two-component heat developable diazotypes |
US3650750A (en) * | 1968-12-28 | 1972-03-21 | Ricoh Kk | Heat-developable diazo-type light-sensitive material |
US4043816A (en) * | 1972-05-26 | 1977-08-23 | Oce-Van Der Grinten N.V. | Photographic process for making diazotype copies utilizing small quantity of liquid developer |
Also Published As
Publication number | Publication date |
---|---|
NL82334C (en(2012)) | |
GB698027A (en) | 1953-10-07 |
ES202557A1 (es) | 1952-04-16 |
FR1058926A (fr) | 1954-03-19 |
DE973598C (de) | 1960-04-07 |
CH307021A (de) | 1955-05-15 |
GB711390A (en) | 1954-06-30 |
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