DE130742C - - Google Patents
Info
- Publication number
- DE130742C DE130742C DE1901130742D DE130742DA DE130742C DE 130742 C DE130742 C DE 130742C DE 1901130742 D DE1901130742 D DE 1901130742D DE 130742D A DE130742D A DE 130742DA DE 130742 C DE130742 C DE 130742C
- Authority
- DE
- Germany
- Prior art keywords
- weight
- parts
- reduction
- alkaline
- copper
- 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
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 230000000875 corresponding Effects 0.000 claims description 3
- 150000001447 alkali salts Chemical class 0.000 claims 1
- 150000002828 nitro derivatives Chemical class 0.000 claims 1
- 239000000243 solution Substances 0.000 description 7
- LQNUZADURLCDLV-UHFFFAOYSA-N Nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 230000005518 electrochemistry Effects 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- XJCVRTZCHMZPBD-UHFFFAOYSA-N 3-Nitroaniline Chemical compound NC1=CC=CC([N+]([O-])=O)=C1 XJCVRTZCHMZPBD-UHFFFAOYSA-N 0.000 description 3
- 229940018564 M-PHENYLENEDIAMINE Drugs 0.000 description 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N M-Phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-Naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
- 239000003929 acidic solution Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 159000000011 group IA salts Chemical class 0.000 description 2
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- RJKGJBPXVHTNJL-UHFFFAOYSA-N 1-nitronaphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=CC2=C1 RJKGJBPXVHTNJL-UHFFFAOYSA-N 0.000 description 1
- PLAZTCDQAHEYBI-UHFFFAOYSA-N 2-Nitrotoluene Chemical compound CC1=CC=CC=C1[N+]([O-])=O PLAZTCDQAHEYBI-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- -1 nitro hydrocarbons Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Electrolytic Production Of Metals (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT10819D AT10819B (it) | 1901-05-14 | 1902-04-18 | |
| AT13089D AT13089B (it) | 1901-05-14 | 1902-06-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE130742C true DE130742C (it) |
Family
ID=399122
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1901130742D Expired - Lifetime DE130742C (it) | 1901-05-14 | 1901-05-14 |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE130742C (it) |
-
1901
- 1901-05-14 DE DE1901130742D patent/DE130742C/de not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1953270B1 (de) | Verfahren zur Leistungsverbesserung von Nickelelektroden | |
| DE69600949T2 (de) | Elektrolytische Extraktion von Blei | |
| DE1543755A1 (de) | Verfahren zur Herstellung von quarternaeren Ammoniumhydroxyden | |
| DE130742C (it) | ||
| DE1222348B (de) | Galvanisches Gold- oder Goldlegierungsbad | |
| DE1270024B (de) | Verfahren zur reduktiven Dimerisierung von Acrylnitril zu Adipinsaeuredinitril | |
| AT113679B (de) | Verfahren zur Darstellung von Aminooxyverbindungen der aromatischen Reihe. | |
| DE75260C (de) | Verfahren zur Darstellung von Amidophenolen durch elektrolytische Reduction von Nitrokohlenwasserstoffen der Benzolreihe in schwefelsaurer Lösung | |
| DE154086C (it) | ||
| RU2556001C1 (ru) | БЕЗДИАФРАГМЕННЫЙ ЭЛЕКТРОСИНТЕЗ ЗАМЕЩЕННЫХ ПИРИДО[1,2-а]БЕНЗИМИДАЗОЛОВ | |
| DE116942C (it) | ||
| DE1695343A1 (de) | Verfahren zur Herstellung von Purinderivaten | |
| DE181116C (it) | ||
| DE168115C (it) | ||
| DE235955C (it) | ||
| AT20189B (de) | Verfahren zur elektrolytischen Darstellung von Azofarbstoffen. | |
| DE437002C (de) | Verfahren zur Darstellung von Aminooxyverbindungen der aromatischen Reihe | |
| DE163842C (it) | ||
| DE102009001168A1 (de) | Verfahren zur Herstellung von Hypophosphiten und Phosphiten | |
| DE592870C (de) | Verfahren zur Herstellung von 3-Amino-4-oxybenzol-1-arsinsaeure | |
| DE174737C (it) | ||
| DE152926C (it) | ||
| DE91707C (it) | ||
| DE973986C (de) | Verfahren zur galvanischen Abscheidung von Indium, insbesondere Indiumueberzuegen | |
| DE1253986B (de) | Saures galvanisches Glanzzinkbad |