US3157503A - Diazotype reproduction materials - Google Patents
Diazotype reproduction materials Download PDFInfo
- Publication number
- US3157503A US3157503A US266231A US26623163A US3157503A US 3157503 A US3157503 A US 3157503A US 266231 A US266231 A US 266231A US 26623163 A US26623163 A US 26623163A US 3157503 A US3157503 A US 3157503A
- Authority
- US
- United States
- Prior art keywords
- support
- layer
- heat
- diazotype
- coated
- 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.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 title description 29
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims description 34
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- 235000010299 hexamethylene tetramine Nutrition 0.000 claims description 17
- 239000004312 hexamethylene tetramine Substances 0.000 claims description 17
- 229960004011 methenamine Drugs 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- 150000001989 diazonium salts Chemical class 0.000 claims description 6
- 230000000694 effects Effects 0.000 claims description 6
- BRWIZMBXBAOCCF-UHFFFAOYSA-N hydrazinecarbothioamide Chemical compound NNC(N)=S BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 claims description 6
- HQDAJGNZGNZGCO-UHFFFAOYSA-N (propan-2-ylideneamino)urea Chemical compound CC(C)=NNC(N)=O HQDAJGNZGNZGCO-UHFFFAOYSA-N 0.000 claims description 5
- UJTTUOLQLCQZEA-UHFFFAOYSA-N 9h-fluoren-9-ylmethyl n-(4-hydroxybutyl)carbamate Chemical compound C1=CC=C2C(COC(=O)NCCCCO)C3=CC=CC=C3C2=C1 UJTTUOLQLCQZEA-UHFFFAOYSA-N 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 230000005855 radiation Effects 0.000 claims description 5
- HCOMFAYPHBFMKU-UHFFFAOYSA-N butanedihydrazide Chemical compound NNC(=O)CCC(=O)NN HCOMFAYPHBFMKU-UHFFFAOYSA-N 0.000 claims description 4
- -1 DIAZO Chemical class 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- GJUITZPINWENSH-UHFFFAOYSA-N [Cl-].[NH4+].NN Chemical compound [Cl-].[NH4+].NN GJUITZPINWENSH-UHFFFAOYSA-N 0.000 claims 1
- 239000000306 component Substances 0.000 description 18
- 239000000243 solution Substances 0.000 description 16
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 10
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 9
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 230000001235 sensitizing effect Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 159000000000 sodium salts Chemical class 0.000 description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- XEVRDFDBXJMZFG-UHFFFAOYSA-N carbonyl dihydrazine Chemical compound NNC(=O)NN XEVRDFDBXJMZFG-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 235000005074 zinc chloride Nutrition 0.000 description 4
- 239000011592 zinc chloride Substances 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 3
- HOPSCVCBEOCPJZ-UHFFFAOYSA-N carboxymethyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC(O)=O HOPSCVCBEOCPJZ-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- JRNGUTKWMSBIBF-UHFFFAOYSA-N naphthalene-2,3-diol Chemical compound C1=CC=C2C=C(O)C(O)=CC2=C1 JRNGUTKWMSBIBF-UHFFFAOYSA-N 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- YSULOORXQBDPCU-UHFFFAOYSA-N 2-(trimethylazaniumyl)ethanehydrazonate;hydrochloride Chemical compound [Cl-].C[N+](C)(C)CC(=O)NN YSULOORXQBDPCU-UHFFFAOYSA-N 0.000 description 1
- CCIAVEMREXZXAK-UHFFFAOYSA-M 4-(dimethylamino)benzenediazonium;chloride Chemical compound [Cl-].CN(C)C1=CC=C([N+]#N)C=C1 CCIAVEMREXZXAK-UHFFFAOYSA-M 0.000 description 1
- DKJVSIITPZVTRO-UHFFFAOYSA-N 6,7-dihydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C=C(O)C(O)=CC2=C1 DKJVSIITPZVTRO-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 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 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- GMCCTOQXFCOXLG-UHFFFAOYSA-M [Cl-].C(C)C1=C(C(=C(C=C1)[N+]#N)N)CCO Chemical compound [Cl-].C(C)C1=C(C(=C(C=C1)[N+]#N)N)CCO GMCCTOQXFCOXLG-UHFFFAOYSA-M 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- CLRSZXHOSMKUIB-UHFFFAOYSA-M benzenediazonium chloride Chemical compound [Cl-].N#[N+]C1=CC=CC=C1 CLRSZXHOSMKUIB-UHFFFAOYSA-M 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- ICLSVWGKWMRCHG-UHFFFAOYSA-N carboxymethyl(trimethyl)azanium;hydrazine;chloride Chemical compound [Cl-].NN.C[N+](C)(C)CC(O)=O ICLSVWGKWMRCHG-UHFFFAOYSA-N 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 150000002897 organic nitrogen compounds Chemical class 0.000 description 1
- 125000001477 organic nitrogen group Chemical group 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- BERQWQSQOIEUMA-UHFFFAOYSA-M sodium;5,7-disulfonaphthalene-2-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(S(O)(=O)=O)=CC2=CC(S(=O)(=O)O)=CC=C21 BERQWQSQOIEUMA-UHFFFAOYSA-M 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
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
- G03C1/61—Compositions containing diazo compounds as photosensitive substances with non-macromolecular additives
- G03C1/615—Substances generating bases
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C1/00—Refining of pig-iron; Cast iron
- C21C1/02—Dephosphorising or desulfurising
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/28—Manufacture of steel in the converter
- C21C5/42—Constructional features of converters
- C21C5/46—Details or accessories
- C21C5/4606—Lances or injectors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01C—RESISTORS
- H01C7/00—Non-adjustable resistors formed as one or more layers or coatings; Non-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material
Definitions
- This invention relates to diazotype reproduction mat rials and to methods for their preparation and use, and refers more particularly to heat-developable two-compo nent photosensitive diazotype reproduction materials and methods for their preparation and use.
- Diazotype reproduction materials are Widely used commercially because of their combined advantages of quality and low cost.
- Two types are generally used: the semiwet developing type and the dry developing type.
- Each has its own inherent disadvantage.
- the handling of a liquid developer is a negative factor.
- the dry developing type the machine requirements for confining and exhausting noxious ammonia fumes are negative factors.
- the loading of concentrated ammonia water and the removal of spent ammonia water from the machine are disagreeable tasks in the daily use of dry developing machines.
- Thermographic reproduction processes have been used to avoid or eliminate some of the disadvantages of the diazotype processes, but they possess other objectionable properties such as the retention of sensitivity to heat even after the desired reproduction has been made. In addition these materials are not necessarily photosensitive.
- the present invention combines the advantages of the diazotype process with that of the thermographic process While avoiding some of the disadvantages of both.
- the quality and low-cost of the diazotype process is combined with the simplicity of development of the thermographic process.
- the use of liquid developers and gaseous ammonia is avoided, and the final reproduction is insensitivejo further application of heat.
- one object is to provide a heat-developable photosensitive diazotype reproduction material which does not have the disadvantages of the prior art.
- Another object of the present invention is to provide a heat-developable two-component photosensitive diazotype reproduction material.
- Another object is to provide a diazotype reproduction material which is developable without the use of liquid developers or gaseous ammonia.
- Another object is to provide a heat-developable reproduction material which, after development is stable to further undesirable development due to the application of heat.
- Another object is to provide a method for the preparation of heat-developable two-component photosensitive diazotype reproduction material.
- Another object is to provide a method for the use of heat-developable two-component photosensitive diazotype reproduction material.
- Another object is to provide a developing sheet for the heat-development of a two-component photosensitive diazotype reproduction material.
- Another object is to provide a method for the use of a developing sheet in the heat-development of a two-component photosensitive diazotype reproduction material.
- Another object of the present invention is to provide a reproduction material which has good quality and low cost.
- FIGURE 1 is a sectional view of a heat-developable ice two-component photosensitive diazotype reproduction material 16 comprising a support 11 and a heat-developable two-component photosensitive diazotype layerlZ coated on said support.
- FIGURE 2 is a sectional view of a heat-developable two-component photosensitive diazotype reproduction material 29 comprising a support 21, a precoat layer 22 coated on said support, and a two component photosensitive diazotype layer 23 coated over said precoat layer on said support.
- FIGURE 3 is a sectional view of a developing sheet 36 comprising a support 31 and a base-releasing agent 32 impregnated in said support in contact With a two-component photosensitive diazotype reproduction material 40 comprising a support 41 and a two-component photosensitive diazotype layer 42 coated on said support.
- thermosensitive base-releasing agents of the present invention is a group of chemical structural formulas of the thermosensitive base-releasing agents of the present invention:
- the base-releasing agent can be incorporated into the sensitized layer, into a separate precoat layer between the support and the sensitized layer, or it can be impregnated into a separate support to make a developing sheet. Compatibility with the other chemicals in the sensitizing solution determines Whether or not it can be incorporated into the various systems. Generally where it is incorporated with the sensi izing solution adjustments are required to prevent precoupling of the diazonium compound and the coupler. Base is released under the influence of heat.
- the agent can either be coated on the same support in a precoat layer between the support and the sensitizing layer or it can ,be coated or impregnated into a separate support to form a developing sheet.
- the base-releasing agents found to be suitable for the present invention are organic nitrogen compounds such 'as hexamethylenetetramine, thiosemicarbazide, and combinations of these with other organic nitrogen com,- pounds. Combinations of hexamethylenetetramine with semicarbazide hydrochloride for example were found to be satisfactory for purposes of the present invention.
- thermosensitive diazotype reproduction materials with the base releasing agent in either the sensitizing layer or a precoat layer is the same. Both are exposed conventionally through a master to actinic radiations to form latent images in the reproduction material. the master, both can be heated in the temperature range between the heat activation temperature of the thermosensitive base-releasing agent and the scorchingtemperature of the reproduction material support. Temperatures of about 140 to 160 C. have been found to be adequate for development purposes.
- the developing sheet In the case of a developing sheet, the developing sheet is placed in face-to-face contact with van exposed twocomponent photosensitive diazotype reproduction material and. the assembly heated preferably from the developing sheet side. The heat releases the base from the base-releasing agent and the base migrates to the exposed diazotype reproduction material and thus permits coupling to take place. Reproduction of the original image is thus effected.
- Example 1 A support was coated with a sensitizing solution prepared according. to the following formula:
- the sensitized support was exposed to actinic radiations through a master and then heated at 160 C. for a few seconds. A red-violet image corresponding to the master image was produced on a yellow background.
- Example 2 Hexamethylenetetramine was used in the following formula to make a precoat solution:
- Example 1 After removal of This was coated on a support and dried.
- Example 3 Hexamethylenetetramine was used in the following solution to prepare a developing sheet:
- Example 5 V A 'precoat solution was prepared according to the following formula:
- a stock solution was prepared according to the following formula:
- a sheet for the thermal development of a photosensitive diazo layer comprising a photosensitive diazonium compound and a coupler therefor, which comprises:
- thermosensitive base-releasing agent selected from the group consisting of: hexamethylene tetramine, thiosemicarbazide, and mixtures of hexamethylene tetramine with one of the following: semicarbazide hydrochloride, carboxymethyl trimethyl ammonium chloride hydrazide, carbohydrazide, succinhydrazide, and acetone semicarbazone coated on said support,
- a sheet for the thermal development of a photosensitive diazo layer comprising a photosensitive diazonium compound and a coupler therefor, which comprises:
- a sheet for the thermal development of a photosensitive diazo layer comprising a photosensitive diazonium compound and a coupler therefor, which comprises:
- thermosensitive base-releasing hexamethylene tetramine coated on said support between said support and said diazo layer thermosensitive base-releasing hexamethylene tetramine coated on said support between said support and said diazo layer.
- a method for thermally developing a photosensitive diazo layer comprising a photosensitive diazonium compound and a coupler therefor, which comprises the steps of:
- thermosensitive base-releasing agent a member selected from the group consisting of: hexamethylene tetramine, thiosemicarbazide, and mixtures of hexamethylene tetramine with one of the following: sernicarbazide hydrochloride, carboxymethyl trimethyl ammonium chloride hydrazine, carbohydrazide, succinhyclrazide, and acetone semicarbazone.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Electromagnetism (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US266231A US3157503A (en) | 1963-03-19 | 1963-03-19 | Diazotype reproduction materials |
DE19641447738 DE1447738A1 (de) | 1963-03-19 | 1964-03-14 | Reproduktionsmaterial fuer die Diazotypie |
BE645320A BE645320A (en)van) | 1963-03-19 | 1964-03-17 | |
NL6402882A NL6402882A (en)van) | 1963-03-19 | 1964-03-18 | |
FR967921A FR1386060A (fr) | 1963-03-19 | 1964-03-19 | Matériel de reproduction pour la diazotypie |
AT622465A AT265016B (de) | 1963-03-19 | 1964-03-19 | Entwicklerbogen für die Wärmeentwicklung von lichtempfindlichem Zweikomponenten-Diazotypiematerial |
AT242264A AT253928B (de) | 1963-03-19 | 1964-03-19 | Wärmeentwickelbares lichtempfindliches Zweikomponenten-Diazotypiematerial |
GB11669/64A GB1060744A (en) | 1963-03-19 | 1964-03-19 | Improvements in and relating to diazotype reproduction |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US266231A US3157503A (en) | 1963-03-19 | 1963-03-19 | Diazotype reproduction materials |
Publications (1)
Publication Number | Publication Date |
---|---|
US3157503A true US3157503A (en) | 1964-11-17 |
Family
ID=23013717
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US266231A Expired - Lifetime US3157503A (en) | 1963-03-19 | 1963-03-19 | Diazotype reproduction materials |
Country Status (7)
Country | Link |
---|---|
US (1) | US3157503A (en)van) |
AT (2) | AT253928B (en)van) |
BE (1) | BE645320A (en)van) |
DE (1) | DE1447738A1 (en)van) |
FR (1) | FR1386060A (en)van) |
GB (1) | GB1060744A (en)van) |
NL (1) | NL6402882A (en)van) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3255011A (en) * | 1963-05-31 | 1966-06-07 | Gen Aniline & Film Corp | Two-component diazotype photoprinting material susceptible to thermal development |
US3318699A (en) * | 1963-10-12 | 1967-05-09 | Keuffel & Esser Co | Process and material for the development of diazotype copies |
US3389995A (en) * | 1964-09-15 | 1968-06-25 | Gen Aniline & Film Corp | Two-component heat developable diazotypes containing amidine compounds |
US3458314A (en) * | 1963-09-25 | 1969-07-29 | Keuffel & Esser Co | Process and device for developing a two-component diazotype material |
US3918974A (en) * | 1970-05-01 | 1975-11-11 | Mita Industrial Co Ltd | Process for the diazo-type multicolor reproduction |
WO1982002689A1 (en) * | 1981-02-13 | 1982-08-19 | Jean J Robillard | Process for forming colored images on textile materials and photosensitive film for use in said process |
US6280913B1 (en) | 2000-06-13 | 2001-08-28 | Eastman Kodak Company | Photographic element comprising an ion exchanged photographically useful compound |
CN114813722A (zh) * | 2022-04-25 | 2022-07-29 | 中国科学院新疆理化技术研究所 | 一种检测乌洛托品的比色试剂 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2653091A (en) * | 1950-01-31 | 1953-09-22 | Rca Corp | Photographic diazotype composition and heat development thereof |
US2732299A (en) * | 1952-07-22 | 1956-01-24 | Light sensitive | |
US2774669A (en) * | 1953-04-13 | 1956-12-18 | Dick Co Ab | Diazotype reproduction process |
GB816601A (en) * | 1954-07-09 | 1959-07-15 | Arnold Tanenbaum | Improvements in or relating to diazotype processes |
FR1249913A (fr) * | 1959-11-23 | 1961-01-06 | Bauchet & Cie Ets | Produit diazotype développable par la chaleur |
US2982675A (en) * | 1955-05-12 | 1961-05-02 | Process Methods Corp | Method of water- and grease-proofing paper products |
-
1963
- 1963-03-19 US US266231A patent/US3157503A/en not_active Expired - Lifetime
-
1964
- 1964-03-14 DE DE19641447738 patent/DE1447738A1/de active Pending
- 1964-03-17 BE BE645320A patent/BE645320A/xx unknown
- 1964-03-18 NL NL6402882A patent/NL6402882A/xx unknown
- 1964-03-19 AT AT242264A patent/AT253928B/de active
- 1964-03-19 FR FR967921A patent/FR1386060A/fr not_active Expired
- 1964-03-19 GB GB11669/64A patent/GB1060744A/en not_active Expired
- 1964-03-19 AT AT622465A patent/AT265016B/de active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2653091A (en) * | 1950-01-31 | 1953-09-22 | Rca Corp | Photographic diazotype composition and heat development thereof |
US2732299A (en) * | 1952-07-22 | 1956-01-24 | Light sensitive | |
US2774669A (en) * | 1953-04-13 | 1956-12-18 | Dick Co Ab | Diazotype reproduction process |
GB816601A (en) * | 1954-07-09 | 1959-07-15 | Arnold Tanenbaum | Improvements in or relating to diazotype processes |
US2982675A (en) * | 1955-05-12 | 1961-05-02 | Process Methods Corp | Method of water- and grease-proofing paper products |
FR1249913A (fr) * | 1959-11-23 | 1961-01-06 | Bauchet & Cie Ets | Produit diazotype développable par la chaleur |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3255011A (en) * | 1963-05-31 | 1966-06-07 | Gen Aniline & Film Corp | Two-component diazotype photoprinting material susceptible to thermal development |
US3458314A (en) * | 1963-09-25 | 1969-07-29 | Keuffel & Esser Co | Process and device for developing a two-component diazotype material |
US3318699A (en) * | 1963-10-12 | 1967-05-09 | Keuffel & Esser Co | Process and material for the development of diazotype copies |
US3389995A (en) * | 1964-09-15 | 1968-06-25 | Gen Aniline & Film Corp | Two-component heat developable diazotypes containing amidine compounds |
US3918974A (en) * | 1970-05-01 | 1975-11-11 | Mita Industrial Co Ltd | Process for the diazo-type multicolor reproduction |
WO1982002689A1 (en) * | 1981-02-13 | 1982-08-19 | Jean J Robillard | Process for forming colored images on textile materials and photosensitive film for use in said process |
US6280913B1 (en) | 2000-06-13 | 2001-08-28 | Eastman Kodak Company | Photographic element comprising an ion exchanged photographically useful compound |
CN114813722A (zh) * | 2022-04-25 | 2022-07-29 | 中国科学院新疆理化技术研究所 | 一种检测乌洛托品的比色试剂 |
Also Published As
Publication number | Publication date |
---|---|
NL6402882A (en)van) | 1964-09-21 |
AT253928B (de) | 1967-04-25 |
GB1060744A (en) | 1967-03-08 |
DE1447738A1 (de) | 1969-03-13 |
FR1386060A (fr) | 1965-01-15 |
AT265016B (de) | 1968-09-25 |
BE645320A (en)van) | 1964-09-17 |
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