US2528395A - Diazotype dry strip film - Google Patents
Diazotype dry strip film Download PDFInfo
- Publication number
- US2528395A US2528395A US719399A US71939946A US2528395A US 2528395 A US2528395 A US 2528395A US 719399 A US719399 A US 719399A US 71939946 A US71939946 A US 71939946A US 2528395 A US2528395 A US 2528395A
- Authority
- US
- United States
- Prior art keywords
- diazotype
- nlm
- film
- plastic
- sensitized
- 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
- 239000011086 glassine Substances 0.000 claims description 12
- 150000008049 diazo compounds Chemical class 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 claims description 7
- 229920006218 cellulose propionate Polymers 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 5
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 4
- 239000002985 plastic film Substances 0.000 claims description 4
- 229920006255 plastic film Polymers 0.000 claims description 4
- -1 POLYISOBUTANOL Polymers 0.000 claims description 2
- 238000006149 azo coupling reaction Methods 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical class C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 claims 1
- 238000000576 coating method Methods 0.000 description 21
- 239000011248 coating agent Substances 0.000 description 20
- 229920003023 plastic Polymers 0.000 description 18
- 239000004033 plastic Substances 0.000 description 18
- 239000000853 adhesive Substances 0.000 description 11
- 230000001070 adhesive effect Effects 0.000 description 11
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 239000002131 composite material Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 229920002301 cellulose acetate Polymers 0.000 description 6
- 229920001727 cellulose butyrate Polymers 0.000 description 6
- 230000008961 swelling Effects 0.000 description 6
- 239000000987 azo dye Substances 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000004014 plasticizer Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 4
- 230000002745 absorbent Effects 0.000 description 4
- 239000002250 absorbent Substances 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 229920002678 cellulose Polymers 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
- 239000003517 fume Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- 230000001235 sensitizing effect Effects 0.000 description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 4
- 229960000834 vinyl ether Drugs 0.000 description 4
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229920003086 cellulose ether Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000005499 meniscus Effects 0.000 description 3
- 230000033458 reproduction Effects 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- 229940123208 Biguanide Drugs 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000004615 ingredient Substances 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
- 230000035515 penetration Effects 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
- ZOZFMTULOYRWEL-UHFFFAOYSA-N (4-bromo-3,5-dimethylphenyl) n-methylcarbamate Chemical compound CNC(=O)OC1=CC(C)=C(Br)C(C)=C1 ZOZFMTULOYRWEL-UHFFFAOYSA-N 0.000 description 1
- AHCDXLAGLYNTIA-UHFFFAOYSA-N 1-n-ethyl-2-methylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(N)C=C1C AHCDXLAGLYNTIA-UHFFFAOYSA-N 0.000 description 1
- RBUQOUQQUQCSAU-UHFFFAOYSA-N 2-(4-aminoanilino)ethanol Chemical compound NC1=CC=C(NCCO)C=C1 RBUQOUQQUQCSAU-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical class C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 description 1
- MTIBLCIOPCKHAL-UHFFFAOYSA-N 3-amino-4-hydroxynaphthalene-2,7-disulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C=C(S(O)(=O)=O)C(N)=C(O)C2=C1 MTIBLCIOPCKHAL-UHFFFAOYSA-N 0.000 description 1
- RXCMFQDTWCCLBL-UHFFFAOYSA-N 4-amino-3-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(N)=C(O)C=C(S(O)(=O)=O)C2=C1 RXCMFQDTWCCLBL-UHFFFAOYSA-N 0.000 description 1
- NIVIKYBSFMJKQM-UHFFFAOYSA-N 4-cyclohexyl-3-methoxycyclohexa-1,5-diene-1,4-diamine Chemical compound NC1=CC(C(N)(C=C1)C1CCCCC1)OC NIVIKYBSFMJKQM-UHFFFAOYSA-N 0.000 description 1
- YZYFPMLAGIGAJJ-UHFFFAOYSA-N 4-diazo-n,n-diethylcyclohexa-1,5-dien-1-amine Chemical compound CCN(CC)C1=CCC(=[N+]=[N-])C=C1 YZYFPMLAGIGAJJ-UHFFFAOYSA-N 0.000 description 1
- SKIBELYSXFYZPS-UHFFFAOYSA-N 4-n-ethylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(N)C=C1 SKIBELYSXFYZPS-UHFFFAOYSA-N 0.000 description 1
- ZYSOYLBBCYWEMB-UHFFFAOYSA-N 7-aminonaphthalen-1-ol Chemical compound C1=CC=C(O)C2=CC(N)=CC=C21 ZYSOYLBBCYWEMB-UHFFFAOYSA-N 0.000 description 1
- LRSYZHFYNDZXMU-UHFFFAOYSA-N 9h-carbazol-3-amine Chemical compound C1=CC=C2C3=CC(N)=CC=C3NC2=C1 LRSYZHFYNDZXMU-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000001243 acetic acids Chemical class 0.000 description 1
- DYRDKSSFIWVSNM-UHFFFAOYSA-N acetoacetanilide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000004674 formic acids Chemical class 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical class [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 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
Definitions
- DIAZOTYPE DRY STRIP FILM Filed Dec. 31, 1946 INVENTOR f1 TTORNEYS Patented Oct. 31, 1950 DIAZTYPE DRY STRIP FILM ⁇ Sam Charles Slifkin, Binghamton, N. Y., assigner to General Aniline & Film Corporation, New York, N.v Y., a lcorporation of Delaware Application December 31, 1946, Serial No. 719,399
- This invention relates to light-sensitive diazotype layers. More particularly, it relates to such layers on a plastic strip nlm base.
- a stripping nlm can be prepared containing ⁇ a diazo photo sensitized layer by means of which the design of a trade-mark label, notice or the like can be conveniently reproduced from a master original. Such reproductions can be made immediately before use, thus the design can be kept up to date as corrections or additions can be made on the master original. If it becomes necessary to make major changes in the design onlythe master original need be replaced.
- the said master original can be made on any transparent or semi-v transparent material such as tracing cloth, plastic nlm, transparentized paper, a stencil design or any similar material wherein the design is opaque to ultraviolet and other actinic light and Ythe background is transmissive of suchlight.
- the new strip nlm is prepared by anxing a plastic nlm to a non-absorbent or poorlyfabsorbent support by means of a pressure sensitive adhesive.
- a composite nlm on support having the form pictured in the accompanying drawing results.
- This composite is thenphoto-sensitized 4 Claims. (Cl. 95-9) on the plastic nlm side by a diazotype sensitizing solution. This is accomplished by the bead dip method of applying diazotype coatings to plastic nlm surfaces or by spraying or otherwise applying an excess of the sensitizing solution and doctoring off the excess with a doctor blade.
- the composite strip nlm is drawn across a vessel containing the diazotype coating solution with the plastic nlm side of the composite in continuous contact with the meniscus of the coating solution.
- the coating solution will contain a solvent or plasticizerfor the plastic nlm material. During the period of Contact of the plastic nlm surface with the meniscus of the coating solution, this solvent or plasticizer will act on the nlm surface to produce a swelling or softening of the nlm.
- the lm is thereby rendered susceptible to penetration and impregnation with the sensitizing Components of the diazctype coating solution and is simultaneously impregnated with such components.
- the plastic nlm employedl is preferably cellulose acetate although other cellulose ester nlms such as cellulose butyrate, cellulose propionate or mixtures of such cellulose esters may be used.
- Other types of plastic nlm such as cellulose ethers, such as cellulose ethyl ether, vinylv yethers and superpolyamides may be used also.
- the particular solvent or plasticizer employed in the coating solution to aid the impregnation or penetration of the nlm surface by the lightsensitive components will depend upon' the nlm material employed.
- typical volatile organic substances which function as swelling agents when used on the commonly known nlm materials listed above include ethyl alcohol, methyl alcohol, butanol, ethyl lactate, isopropanol, formic and acetic acids, acetone, diacetone alcohol, ethylmethyl ketone and methyl glycol.
- Softeners or plasticizers which may be used include tricresyl phosphate, tri-phenyl phosphate, tri-acetin and di-chlorhydrin.
- the swelling medium or solvent for the plastic nlm may be employed singly, in combination with a Yknown solvent such as water, benzene or toluene or it may be formed from a plurality of the swelling agents or solvents depending upon the nature of the plasticizer and the composition of the plastic nlm. Manifestly,rthere is no set rule for determining the proportions of the' respective ingredients of the swelling medium. However, I have found that a mixture of water and alcohol is particularly effective for this purpose and I prefer to use this mixture in a proportion of two to one by volume.
- the adhesive which is used for aixing the plastic film to the non-absorbent base may be any pressure sensitive adhesive of the resin type such as rubber latex, polyvinyl alcohol, vinyl ether resins and polyisobutynol and the support or base material may be any non-absorbent or poorly absorbent material which is preferably sufciently flexible to permit rolling and passage through a printing and developing machine of the type commonly used in exposing and developing diazotypes.
- Examples of such material are glassine paper, lacquered paper, cellophane, cellulose ester and cellulose ether and film base materials such as those given as examples for the sensitized lm of the composite strip lm.
- diazoand azo components which is suitable for 'the preparation of two-component diazotype layers and which wil1 produce the shade desired for the final image may be employed.
- Diazo compounds which are suitable for such two-component diazotype layers are known to be those which are derived from 1,2 and 2,1-aminonaphthols,p1,4 aminonaphthols and aromatic p-diamines of the benzene series, particularly p-phenylene diamines which are N-mono or di-substituted on one of the amino groups.
- diazo compounds which are commonly used in the production of diazotype images are the diazo derivatives of p-amino N methylaniline; p amino-N-dimethylaniline; p-amino-N-ethylaniline, p-amino-N-diethylaniline, p-amino-N-hydroxyethyl aniline; p-amino N ethyl-N-hydroxyethyl aniline; 4-amino-2-methoxy-l-cyclohexyl aniline; 1-amino-4-(dibrom 26 benzyl)- aminobenzene; p-amino-N-diethyl-m-toluidine; 1amino 3 methyl -4- ethylaminobenzene; 3- aminocarbazole; 1-amino-2-naphthol-4-sulfonic acid and 2-amino-l-hydroxy-3,6naphthalene disulfonic acid
- suitable azo coupling components there may be mentioned the sodium salt of 2-amino-S-naphthol-S-disulfonic acid, 2,3- dihydroxynaphthalene or its 6-sulfonic acid derivative, -naphthol-B-disulfonic acid, 2,7-dihydroxynaphthalene, 1,7aminonaphthol,2 -hydroxy-S-biguanide, lamino8-naphthol-3,6di sulfonic acid, l-naphthol-Ll-sulfonic acid, 1- naphthol-3,8disulfonic acid, phloroglucinol, mhydroxyphenyl-urea, acetoacetanilide, 'I -hydroxy- 1,2-naphthimidazole, 7-hydroxynaphthalene-1- biguanide and acetoacetcyclohexyl-amide After the plastic film surface of the strip film composite
- a diazotype image may be applied to many types of surfaces such as the metal surfaces of machines mentioned above, glass, tile, wood, plaster, or anywhere that an adhesive-back strip film may be applied.
- the sensitized surface of the film is exposed to actinic light in the same manner as any diazotype surface under the picture or design to be reproduced. After so exposing the sensitized surface, the image is developed by treatment with ammonia fumes.
- the strip'film containing the developed image of the design is then stripped 01T of its support and refastened to the desired surface vby means of the adhesive remaining on the underside of thev stripped lm.
- the sensitized plastic film may be stripped from its support, applied to a sheet of metal, wood, or other such surface, and then exposed under the original of the desired pattern and developed by contacting the exposed surface with ammonia fumes.
- a dimensionally correct phototemplate may be made which can be subsequently stripped from the metal or wood surface when the necessary work has been completed.
- Example 1 A composite strip film comprising a cellulose acetate lm adhesively afxed to a glassine support by means of a polyvinyl alcohol adhesive is drawn across the surface of a diazotype coating solution containing the following ingredients:
- Example 2 A strip film made by adhesively afxing a cellulose butyrate film to a glassine base by means of an adhesive polyisobutanol is sensitized on the exposed surface of the cellulose butyrate film by means of the following Adiazotype coating solution:
- Example 3 A strip nlm composite made up by adhesiveiy ailxng a sheet of cellulose propionate film onto a glassine support by means oi a Vinylether resin adhesive is sensitized bythe following diazotype coating solution.
- any of the diazo compounds orl azo components listed above, or any other diazo compounds or azo components known to the art for use in diazotype layers, may be subas may be necessary for the production of a sta-y ble diazotype layer may be substituted for those speciically mentioned in the examples.
- a composition of matter comprising a plastic nlm of the class consisting of cellulose acetate, cellulose butyrate, and cellulose propionate, sensitized on one side with a diazotype layer containing a light-sensitive diazo compound of a pphenylenediamine and an azo dye coupling component, said iilm being afxed on its other side to a glassine support by a pressure-sensitive adhesive of the class consisting of polyvinyl alcohol, polyisobutanol, and vinyl ether resin.
- a composition of matter comprising a cellulose acetate plastic lm sensitized on one side with a .diazotype layer containing a light-sensitive diazo compound of a p-phenylenediamine and an azo dye coupling component, said lm being ali'lxed on its other side to a glassine support by polyvinyl alcohol adhesive.
- a composition of matter comprising Ya cellulose butyrate plastic lm sensitized on one side with a diazotype layer containing a light-sensitive diazo compound of a p-phenylenediamine and an azo dye coupling component, said nlm being afxed on its other side to a glassine support A by polyisobutanol adhesive.
- plastic lm commonly used for 1 may be used in place of the alcohols specically mentioned in these examples to the extent thatthey are compatible in the light-sensitive solution and do not create interfering side reactions.
- a composition of matter comprising a cellulose propionate plastic nlm sensitized on one side with a diazotype layer containing a light-sensitive diazo compound of a p-phenylenediamine and an azo dye coupling component, ⁇ said filmbeing afxed on its other side to a glassine support by vinyl ether resin adhesive.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR961892D FR961892A (en, 2012) | 1946-12-31 | ||
US719399A US2528395A (en) | 1946-12-31 | 1946-12-31 | Diazotype dry strip film |
GB32352/47A GB641273A (en) | 1946-12-31 | 1947-12-08 | Diazotype dry strip film |
DEP29385D DE813940C (de) | 1946-12-31 | 1949-03-01 | Lichtempfindliche Schichten fuer das Diazotypieverfahren |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US719399A US2528395A (en) | 1946-12-31 | 1946-12-31 | Diazotype dry strip film |
Publications (1)
Publication Number | Publication Date |
---|---|
US2528395A true US2528395A (en) | 1950-10-31 |
Family
ID=24889916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US719399A Expired - Lifetime US2528395A (en) | 1946-12-31 | 1946-12-31 | Diazotype dry strip film |
Country Status (4)
Country | Link |
---|---|
US (1) | US2528395A (en, 2012) |
DE (1) | DE813940C (en, 2012) |
FR (1) | FR961892A (en, 2012) |
GB (1) | GB641273A (en, 2012) |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3135608A (en) * | 1960-02-17 | 1964-06-02 | Avery Adhesive Products Inc | Pressure-sensitive wet-process photographic paper |
US3352677A (en) * | 1963-06-24 | 1967-11-14 | Gen Aniline & Film Corp | Transparentizing base stock of tracing papers and intermediate diazotype papers by use of polypropenes |
US3431109A (en) * | 1964-10-16 | 1969-03-04 | Addressograph Multigraph | Heat sensitive diazotype materials |
US3536490A (en) * | 1964-04-28 | 1970-10-27 | Pitney Bowes Inc | Novel diazotype copying process |
US3907557A (en) * | 1971-02-08 | 1975-09-23 | Avery Products Corp | Pressure-sensitive electrostatic imaging labels |
US4216286A (en) * | 1978-09-07 | 1980-08-05 | Greene J Jerrold | Method of laminating cloth with photographic emulsion |
US4268601A (en) * | 1977-07-15 | 1981-05-19 | Fuji Photo Film Co., Ltd. | Photosensitive image forming material and an image forming method using same |
US4331727A (en) * | 1975-09-17 | 1982-05-25 | Stanley Maas | Adhesive transfer device |
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 |
US4599295A (en) * | 1982-10-07 | 1986-07-08 | Dainippon Screen Seizo K.K. | Photosensitive material with two photosensitive layers for forming separate imaged elements |
US4650738A (en) * | 1984-10-22 | 1987-03-17 | American Hoechst Corporation | Negative working diazo color proofing method |
US4659642A (en) * | 1984-10-22 | 1987-04-21 | American Hoechst Corporation | Positive working naphthoquinone diazide color proofing transfer process |
US4680250A (en) * | 1982-12-06 | 1987-07-14 | Nippon Foil Manufacturing Co., Ltd. | Composite aluminum sheet for presensitized lithographic printing plate comprising a support having specified center line average roughness |
US4980260A (en) * | 1987-04-23 | 1990-12-25 | Fuji Photo Film Co., Ltd. | Multi-color image-forming method with microcapsule positive diazotype color image formation and positive light-solubilizing color image formation |
US5094931A (en) * | 1987-04-15 | 1992-03-10 | Hoechst Celanese Corporation | Image transfer to diverse paper stocks |
US5139917A (en) * | 1990-04-05 | 1992-08-18 | Foto-Wear, Inc. | Imaging transfer system and process for transferring image and non-image areas thereof to a receptor element |
US5192630A (en) * | 1987-04-15 | 1993-03-09 | Hoechst Celanese Corporation | Image transfer to diverse paper stocks |
US5236801A (en) * | 1990-04-05 | 1993-08-17 | Foto-Wear, Inc. | Imaging transfer system and process for transferring image and non-image areas thereof to a receptor element |
US5620548A (en) * | 1989-09-11 | 1997-04-15 | Foto-Wear, Inc. | Method for transferring a silver halide photographic transfer element to a receptor surface |
US6022440A (en) * | 1997-12-08 | 2000-02-08 | Imation Corp. | Image transfer process for ink-jet generated images |
US6335067B1 (en) | 1998-08-03 | 2002-01-01 | Xyron, Inc. | Adhesive transfer device |
US6403185B1 (en) * | 1998-06-30 | 2002-06-11 | Xyron, Inc. | Adhesive transfer device for making repositionably adherable substrates |
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GB337868A (en) * | 1929-08-24 | 1930-11-13 | Humphrey Desmond Murray | Improvements in and relating to the manufacture of sensitized bases for photographic purposes |
US2010188A (en) * | 1931-04-15 | 1935-08-06 | Agfa Ansco Corp | Process of fastening photographic films on supports and article produced thereby |
US2089460A (en) * | 1933-02-15 | 1937-08-10 | Agfa Ansco Corp | Process for fastening a photographic material on a support and the resulting product |
US2140648A (en) * | 1936-05-16 | 1938-12-20 | Eastman Kodak Co | Photographic stripping film |
US2216735A (en) * | 1938-09-27 | 1940-10-08 | Du Pont | Photographic film |
GB536714A (en) * | 1940-04-15 | 1941-05-23 | Le Film Ozaphane Sa | Improvements in or relating to light-sensitive photographic films |
US2246425A (en) * | 1938-06-18 | 1941-06-17 | Kalle & Co Ag | Production of diazotype reflex copies |
US2266435A (en) * | 1941-03-20 | 1941-12-16 | Eastman Kodak Co | Photographic stripping film |
US2409564A (en) * | 1941-05-28 | 1946-10-15 | Noc Mfg Company Di | Transfer material |
-
0
- FR FR961892D patent/FR961892A/fr not_active Expired
-
1946
- 1946-12-31 US US719399A patent/US2528395A/en not_active Expired - Lifetime
-
1947
- 1947-12-08 GB GB32352/47A patent/GB641273A/en not_active Expired
-
1949
- 1949-03-01 DE DEP29385D patent/DE813940C/de not_active Expired
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB337868A (en) * | 1929-08-24 | 1930-11-13 | Humphrey Desmond Murray | Improvements in and relating to the manufacture of sensitized bases for photographic purposes |
US2010188A (en) * | 1931-04-15 | 1935-08-06 | Agfa Ansco Corp | Process of fastening photographic films on supports and article produced thereby |
US2089460A (en) * | 1933-02-15 | 1937-08-10 | Agfa Ansco Corp | Process for fastening a photographic material on a support and the resulting product |
US2140648A (en) * | 1936-05-16 | 1938-12-20 | Eastman Kodak Co | Photographic stripping film |
US2246425A (en) * | 1938-06-18 | 1941-06-17 | Kalle & Co Ag | Production of diazotype reflex copies |
US2216735A (en) * | 1938-09-27 | 1940-10-08 | Du Pont | Photographic film |
GB536714A (en) * | 1940-04-15 | 1941-05-23 | Le Film Ozaphane Sa | Improvements in or relating to light-sensitive photographic films |
US2266435A (en) * | 1941-03-20 | 1941-12-16 | Eastman Kodak Co | Photographic stripping film |
US2409564A (en) * | 1941-05-28 | 1946-10-15 | Noc Mfg Company Di | Transfer material |
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3135608A (en) * | 1960-02-17 | 1964-06-02 | Avery Adhesive Products Inc | Pressure-sensitive wet-process photographic paper |
US3352677A (en) * | 1963-06-24 | 1967-11-14 | Gen Aniline & Film Corp | Transparentizing base stock of tracing papers and intermediate diazotype papers by use of polypropenes |
US3536490A (en) * | 1964-04-28 | 1970-10-27 | Pitney Bowes Inc | Novel diazotype copying process |
US3431109A (en) * | 1964-10-16 | 1969-03-04 | Addressograph Multigraph | Heat sensitive diazotype materials |
US3907557A (en) * | 1971-02-08 | 1975-09-23 | Avery Products Corp | Pressure-sensitive electrostatic imaging labels |
US4331727A (en) * | 1975-09-17 | 1982-05-25 | Stanley Maas | Adhesive transfer device |
US4268601A (en) * | 1977-07-15 | 1981-05-19 | Fuji Photo Film Co., Ltd. | Photosensitive image forming material and an image forming method using same |
US4216286A (en) * | 1978-09-07 | 1980-08-05 | Greene J Jerrold | Method of laminating cloth with photographic emulsion |
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 |
US4599295A (en) * | 1982-10-07 | 1986-07-08 | Dainippon Screen Seizo K.K. | Photosensitive material with two photosensitive layers for forming separate imaged elements |
US4680250A (en) * | 1982-12-06 | 1987-07-14 | Nippon Foil Manufacturing Co., Ltd. | Composite aluminum sheet for presensitized lithographic printing plate comprising a support having specified center line average roughness |
US4650738A (en) * | 1984-10-22 | 1987-03-17 | American Hoechst Corporation | Negative working diazo color proofing method |
US4659642A (en) * | 1984-10-22 | 1987-04-21 | American Hoechst Corporation | Positive working naphthoquinone diazide color proofing transfer process |
US5094931A (en) * | 1987-04-15 | 1992-03-10 | Hoechst Celanese Corporation | Image transfer to diverse paper stocks |
US5192630A (en) * | 1987-04-15 | 1993-03-09 | Hoechst Celanese Corporation | Image transfer to diverse paper stocks |
US4980260A (en) * | 1987-04-23 | 1990-12-25 | Fuji Photo Film Co., Ltd. | Multi-color image-forming method with microcapsule positive diazotype color image formation and positive light-solubilizing color image formation |
US6258448B1 (en) | 1989-09-11 | 2001-07-10 | Foto-Wear, Inc. | Silver halide photographic transfer element |
US5620548A (en) * | 1989-09-11 | 1997-04-15 | Foto-Wear, Inc. | Method for transferring a silver halide photographic transfer element to a receptor surface |
US5139917A (en) * | 1990-04-05 | 1992-08-18 | Foto-Wear, Inc. | Imaging transfer system and process for transferring image and non-image areas thereof to a receptor element |
US5236801A (en) * | 1990-04-05 | 1993-08-17 | Foto-Wear, Inc. | Imaging transfer system and process for transferring image and non-image areas thereof to a receptor element |
US6022440A (en) * | 1997-12-08 | 2000-02-08 | Imation Corp. | Image transfer process for ink-jet generated images |
US6403185B1 (en) * | 1998-06-30 | 2002-06-11 | Xyron, Inc. | Adhesive transfer device for making repositionably adherable substrates |
US6660120B2 (en) | 1998-06-30 | 2003-12-09 | Xyron, Inc. | Adhesive transfer device |
US20040062924A1 (en) * | 1998-06-30 | 2004-04-01 | Xyron, Inc. | Adhesive transfer device |
US7087280B2 (en) | 1998-06-30 | 2006-08-08 | Xyron, Inc. | Adhesive transfer device |
US20060263563A1 (en) * | 1998-06-30 | 2006-11-23 | Xyron, Inc. | Adhesive transfer device |
US6335067B1 (en) | 1998-08-03 | 2002-01-01 | Xyron, Inc. | Adhesive transfer device |
Also Published As
Publication number | Publication date |
---|---|
DE813940C (de) | 1951-09-17 |
FR961892A (en, 2012) | 1950-05-24 |
GB641273A (en) | 1950-08-09 |
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