US2100063A - Process for the production of tanned pictures - Google Patents
Process for the production of tanned pictures Download PDFInfo
- Publication number
- US2100063A US2100063A US644920A US64492032A US2100063A US 2100063 A US2100063 A US 2100063A US 644920 A US644920 A US 644920A US 64492032 A US64492032 A US 64492032A US 2100063 A US2100063 A US 2100063A
- Authority
- US
- United States
- Prior art keywords
- light
- tanned
- pictures
- diazo
- production
- 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
- 238000000034 method Methods 0.000 title description 9
- 238000004519 manufacturing process Methods 0.000 title description 6
- 150000008049 diazo compounds Chemical class 0.000 description 13
- 239000000084 colloidal system Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- -1 N-phenyl-4-amino-4'-hydroxy-1.1 diphenylmethane Chemical compound 0.000 description 3
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000001828 Gelatine Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000002837 carbocyclic group Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 201000004624 Dermatitis Diseases 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- JPIYZTWMUGTEHX-UHFFFAOYSA-N auramine O free base Chemical compound C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 JPIYZTWMUGTEHX-UHFFFAOYSA-N 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- IINNWAYUJNWZRM-UHFFFAOYSA-L erythrosin B Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 IINNWAYUJNWZRM-UHFFFAOYSA-L 0.000 description 1
- 229940011411 erythrosine Drugs 0.000 description 1
- 235000012732 erythrosine Nutrition 0.000 description 1
- 239000004174 erythrosine Substances 0.000 description 1
- 239000012213 gelatinous substance Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 150000002605 large molecules Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- NJPKYOIXTSGVAN-UHFFFAOYSA-K trisodium;naphthalene-1,3,6-trisulfonate Chemical compound [Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC(S([O-])(=O)=O)=CC2=CC(S(=O)(=O)[O-])=CC=C21 NJPKYOIXTSGVAN-UHFFFAOYSA-K 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/016—Diazonium salts or compounds
Definitions
- the present invention relates to light-sensitive material, particularly for the preparation of pietures to be produced by tanning action.
- One object of my invention are light-sensitive colloid layers which are adapted to yield after exposure to light, so-called tanned pictures.
- These light-sensitive layers are obtained by incorporating in an organic colloidal material a light-sensitive diazo compound of high molecular 1 weight the light-decomposition products of which are capable of directly tanning the colloidal material.
- the colloidal material thus sensitized is then brought upon a suitable support there forming the sensitive layer, or'it is used as such to 15 form an independent layer or film.
- the use of the said diazo compounds of high molecular weight involves the advantage that the colloids are already tanned during the exposure, without it being necessary, as in. the known processes, to 20 subsequently treat the exposed layers with a chrom'ate or the like. It is thus possibleto avoid the use particularly of the poisonous chromates which frequently produce disagreeable eczema, which is, 01 course, prejudicial to their utilizat- 25 tion in practice.
- Light-sensitive diazo compounds whose lightdecomposition products are capable of tanning colloids are generally those possessing a fairly large molecule, for instance: the diazo com- 30 pounds of 4-amino-1(N-methyl-S-naphthalenetetrahydride-1.2.3.4) -aminobenzene having the formula:
- the diazo compounds suitable for the present invention contain at least three six-membered carbocyclic rings and are constituted according to the following general formula:
- cellulose esters water-insoluble cellulose ethers or regenerated cellulose.
- the preparation of the light-sensitive colloid layers can be adapted in the usual manner to the particular purpose to which they are to be applied.
- a feebly acidified solution of one of the above diazo compounds is added to a colloidal substance colored with a finely divided inorganic or organic pigment, the emulsion is cast on paper and dried.
- a solution of methyl cellulose is colored with a pigment, sensitized as above described and applied in a thin layer on paper.
- the exposed material is developed by treatment with a solvent for the colloid. If, for instance, gelatine is employed as colloidal substance, the colloid at the places not struck by light may be dissolved with the aid of warm water.
- the process of this invention is intended to be used in those cases where hitherto chromates were used for the preparation of pictures to be produced. by tanning action.
- emulsion is prepared from 10 grams of gelatine, 1.5 grams of iron oxide red, 0.8 gram of the zinc chloride double salt of the diazo compound of 4-amino-1(N-methyl-B-naphthalenetetrahydride-1.2.3.4) -aminobenzene, 2 grams of acetic acid of 50 per cent strength and 80 grams of water. It is applied on paper. After drying, a pigment paper is obtained which, after exposure to light, is transferred in the usual manner with the aid of cold water on another support where it can be developed with water of about 40 C.
- aqueous solution of water-soluble methylcellulose are finely triturated with 1 gram of soot; a solution of 0.5 gram of a diazo compound, obtainable by condensing para-formaldehyde with the sulfate of 4-diazo-1.1'-diphenylamine, and 0.7 gram 'of citric acid in 50 grams of water is then added.
- the mixture thus obtained is applied on to paper and dried.
- the finished paper is exposed to light under a pattern; a negative picture of the pattern may be developed with the aid of cold water.
- diazo compound comprises tetrazo compounds also and, furthermore, the said compounds not only as such but also their salts or double salts with acids, salts or the like.
- Process for the production of tanned pictures which comprises exposing under a pattern a light-sensitive layer comprising a colloidal substance capable of being tanned and a lightsensitive aromatic diazo compound of high molecular weight, which contains at least three sixmembered carbocyclic rings and is constituted according to the formula R X-R1, wherein X stands for a member of the group consisting of CH2, oxygen and an imino group and R and R1 for a radical of the group consisting of aromatic and hydroaromatic radicals of the benzene and naphthalene series atleast one of which contains a diazo group, and then dissolving the colloid at the unexposed parts.
- Process for the production of tanned pictures which comprises exposing under a pattern a light-sensitive layer comprising a colloidal substance capable of being tanned and a lightsensitive condensation product obtained by condensing 4'-diazo-1.1'-diphenylamine with. paraformaldehyde and then dissolving the colloid at the unexposed parts.
- Process for the production of tanned pictures which comprises exposing under a pattern a light-sensitive layer comprising a colloidal sub stance capable of being tanned and the diazo compound of 4 -amino-2 -carboxy-1 -N-pheny1-4-amino-4'-hydroxy 1.1 diphenyl-methane and then dissolving the colloid at the unexposed parts.
- Process for the production of tanned pictures which comprises exposing under a pattern a light-sensitive layer comprising a gelatinous substance capable of being tanned and a light-sensitive aromatic diazo compound of high RUDOLF ZAHN.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE401898X | 1931-12-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2100063A true US2100063A (en) | 1937-11-23 |
Family
ID=6408364
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US644920A Expired - Lifetime US2100063A (en) | 1931-12-09 | 1932-11-29 | Process for the production of tanned pictures |
Country Status (5)
Country | Link |
---|---|
US (1) | US2100063A (en)) |
BE (1) | BE392892A (en)) |
FR (1) | FR747246A (en)) |
GB (1) | GB401898A (en)) |
NL (1) | NL35423C (en)) |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2498722A (en) * | 1945-07-04 | 1950-02-28 | Gen Aniline & Film Corp | Solid diazo complexes |
US2605182A (en) * | 1947-11-28 | 1952-07-29 | Gen Aniline & Film Corp | Diazotypes containing n-substituted p-diazoanilines having radicals of at least four conjugated c-c double bonds as n-substituents |
US2606117A (en) * | 1947-06-05 | 1952-08-05 | Gen Aniline & Film Corp | Diazotype photoprinting materials |
US2649373A (en) * | 1948-10-18 | 1953-08-18 | Warren S D Co | Paper printing foils for lithographic purposes and a process of preparing them |
US2690968A (en) * | 1952-10-04 | 1954-10-05 | Powers Chemco Inc | Development of diazo and azide sensitized colloids |
US2695846A (en) * | 1952-11-04 | 1954-11-30 | Powers Chemco Inc | Developing of diazo and azide sensitized colloids |
US2819164A (en) * | 1952-11-29 | 1958-01-07 | Philips Corp | Method of manufacturing metallic patterns |
US2914404A (en) * | 1953-07-31 | 1959-11-24 | Blaupunkt Werke Gmbh | Method of producing two-dimensional circuits or circuit elements on supporting bases |
US2922715A (en) * | 1956-03-26 | 1960-01-26 | Polychrome Corp | Presensitized printing plate and method for preparing same |
US2937085A (en) * | 1954-01-11 | 1960-05-17 | Ditto Inc | Composite photosensitive plate, and method of making printing plate therefrom |
US3010389A (en) * | 1953-03-09 | 1961-11-28 | Buskes Willem Marie | Photographic transfer printing plates |
US3010390A (en) * | 1954-06-29 | 1961-11-28 | Buskes Willem Marie | Planographic printing plates |
US3010391A (en) * | 1954-06-29 | 1961-11-28 | Grinten Chem L V D | Light-sensitive sheets and process for producing transfer images |
US3085008A (en) * | 1957-01-04 | 1963-04-09 | Minnesota Mining & Mfg | Positively-acting diazo planographic printing plate |
US3091528A (en) * | 1958-08-19 | 1963-05-28 | Chem Fab L Van Der Grinten N V | Process and light-sensitive sheets for the production of pigment images by transfer |
US3136636A (en) * | 1950-12-06 | 1964-06-09 | Minnesota Mining & Mfg | Planographic printing plate comprising a polyacid organic intermediate layer |
US3235382A (en) * | 1962-04-03 | 1966-02-15 | Kalle Ag | Presensitized foil for planographic and offset printing |
US3246986A (en) * | 1961-08-07 | 1966-04-19 | Azoplate Corp | Diazo materials for screen process printing |
US3246984A (en) * | 1961-03-09 | 1966-04-19 | Polaroid Corp | Photographic processes and products |
US3294533A (en) * | 1962-05-02 | 1966-12-27 | Azoplate Corp | Presensitized printing plate and process of developing printing plate |
US3375113A (en) * | 1962-09-21 | 1968-03-26 | Scott Paper Co | Sensitizing planographic plates for photo-lithography |
US4247615A (en) * | 1980-03-06 | 1981-01-27 | Eastman Kodak Company | Continuous-tone dyed diazo imaging process |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2754209A (en) * | 1952-06-10 | 1956-07-10 | Azoplate Corp | Light-sensitive para quinone diazides for making printing plates |
GB733409A (en) * | 1952-12-10 | 1955-07-13 | Kalle & Co Ag | Light-sensitive material for photomechanical reproduction and process of making images |
IT979722B (it) * | 1972-03-05 | 1974-09-30 | Somar Mfg | Materiale fotografico e metodo di trattamento per esso |
JPS527364B2 (en)) * | 1973-07-23 | 1977-03-02 |
-
0
- NL NL35423D patent/NL35423C/xx active
- BE BE392892D patent/BE392892A/xx unknown
-
1932
- 1932-11-29 US US644920A patent/US2100063A/en not_active Expired - Lifetime
- 1932-12-08 GB GB34893/32A patent/GB401898A/en not_active Expired
- 1932-12-09 FR FR747246D patent/FR747246A/fr not_active Expired
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2498722A (en) * | 1945-07-04 | 1950-02-28 | Gen Aniline & Film Corp | Solid diazo complexes |
US2606117A (en) * | 1947-06-05 | 1952-08-05 | Gen Aniline & Film Corp | Diazotype photoprinting materials |
US2605182A (en) * | 1947-11-28 | 1952-07-29 | Gen Aniline & Film Corp | Diazotypes containing n-substituted p-diazoanilines having radicals of at least four conjugated c-c double bonds as n-substituents |
US2649373A (en) * | 1948-10-18 | 1953-08-18 | Warren S D Co | Paper printing foils for lithographic purposes and a process of preparing them |
US3136636A (en) * | 1950-12-06 | 1964-06-09 | Minnesota Mining & Mfg | Planographic printing plate comprising a polyacid organic intermediate layer |
US2690968A (en) * | 1952-10-04 | 1954-10-05 | Powers Chemco Inc | Development of diazo and azide sensitized colloids |
US2695846A (en) * | 1952-11-04 | 1954-11-30 | Powers Chemco Inc | Developing of diazo and azide sensitized colloids |
US2819164A (en) * | 1952-11-29 | 1958-01-07 | Philips Corp | Method of manufacturing metallic patterns |
US3010389A (en) * | 1953-03-09 | 1961-11-28 | Buskes Willem Marie | Photographic transfer printing plates |
US2914404A (en) * | 1953-07-31 | 1959-11-24 | Blaupunkt Werke Gmbh | Method of producing two-dimensional circuits or circuit elements on supporting bases |
US2937085A (en) * | 1954-01-11 | 1960-05-17 | Ditto Inc | Composite photosensitive plate, and method of making printing plate therefrom |
US3010390A (en) * | 1954-06-29 | 1961-11-28 | Buskes Willem Marie | Planographic printing plates |
US3010391A (en) * | 1954-06-29 | 1961-11-28 | Grinten Chem L V D | Light-sensitive sheets and process for producing transfer images |
US2922715A (en) * | 1956-03-26 | 1960-01-26 | Polychrome Corp | Presensitized printing plate and method for preparing same |
US3085008A (en) * | 1957-01-04 | 1963-04-09 | Minnesota Mining & Mfg | Positively-acting diazo planographic printing plate |
US3091528A (en) * | 1958-08-19 | 1963-05-28 | Chem Fab L Van Der Grinten N V | Process and light-sensitive sheets for the production of pigment images by transfer |
US3246984A (en) * | 1961-03-09 | 1966-04-19 | Polaroid Corp | Photographic processes and products |
US3246986A (en) * | 1961-08-07 | 1966-04-19 | Azoplate Corp | Diazo materials for screen process printing |
US3235382A (en) * | 1962-04-03 | 1966-02-15 | Kalle Ag | Presensitized foil for planographic and offset printing |
US3294533A (en) * | 1962-05-02 | 1966-12-27 | Azoplate Corp | Presensitized printing plate and process of developing printing plate |
US3375113A (en) * | 1962-09-21 | 1968-03-26 | Scott Paper Co | Sensitizing planographic plates for photo-lithography |
US4247615A (en) * | 1980-03-06 | 1981-01-27 | Eastman Kodak Company | Continuous-tone dyed diazo imaging process |
Also Published As
Publication number | Publication date |
---|---|
FR747246A (fr) | 1933-06-13 |
GB401898A (en) | 1933-11-23 |
NL35423C (en)) | |
BE392892A (en)) |
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