US322940A - Theodor kempf - Google Patents
Theodor kempf Download PDFInfo
- Publication number
- US322940A US322940A US322940DA US322940A US 322940 A US322940 A US 322940A US 322940D A US322940D A US 322940DA US 322940 A US322940 A US 322940A
- Authority
- US
- United States
- Prior art keywords
- iodoform
- theodor
- kempf
- dated
- bromoform
- 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
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 18
- 229960003172 iodoform Drugs 0.000 description 18
- HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 16
- DIKBFYAXUHHXCS-UHFFFAOYSA-N Bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 description 10
- 229950005228 bromoform Drugs 0.000 description 10
- 238000005868 electrolysis reaction Methods 0.000 description 8
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 8
- 229910052700 potassium Inorganic materials 0.000 description 8
- 239000011591 potassium Substances 0.000 description 8
- 238000000354 decomposition reaction Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 6
- 150000002367 halogens Chemical class 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 230000001476 alcoholic Effects 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 230000000875 corresponding Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 229960001701 Chloroform Drugs 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/34—Simultaneous production of alkali metal hydroxides and chlorine, oxyacids or salts of chlorine, e.g. by chlor-alkali electrolysis
- C25B1/46—Simultaneous production of alkali metal hydroxides and chlorine, oxyacids or salts of chlorine, e.g. by chlor-alkali electrolysis in diaphragm cells
Definitions
- This invention relates to the production of iodoform, bromoform, and chloroform by electrolysis from the corresponding halogen combinations of the alkalies and alkaline earths in the presence of alcohol, aldehyde, or acetone and heat.
- I dissolve fifty kilograms of iodide of potassium in about three hundred kilograms ofwater, to which I add about thirty kilograms of alcohol of ninety-six per cent.
- This solution is then subjected to electrolysis in a suitable Vessel under a continuous introduction of carbonic acid and the application of heat.
- the iodoform obtained separates from the solution in a crystalline powder.
- the iodide of potassium is dissolved in about twenty per cent. of alcohol, and subjected to the electrolysis described.
Description
NITED STATES T T FFICEQ THEODOR KEMPF, OF BERLIN, GERMANY, ASSIGNOR TO THE CHEMISCHE FABRIK AUF AOTIEN, OF SAME PLACE.
MANUFACTURE OF IODOFORM, BROMOFORM, AND CHLOROFORM.
SPECIFICATION forming part of Letters Patent No. 322,940, dated July 28, 1885.
Application filed June 5,1884. (No specimens.) Patented in Germany March 7, 1884, No. 29,771; in England May 23, 1884,170. 8,148; in France May 23, 1884, No. 162,306; in Belgium May 23,1884, No. 65,227; in Luxemburg May 24, 1884, No. 405, and in Austria-Hungary September 23, 1884, No, 19,725 and No. 42,228.
To all whom it may concern.-
Be it known that I, THEODOR KEMPF, a subject of the King of Prussia, residing at Berlin, Prussia, German Empire, have invented certain new and useful Improvements in the Process of Manufacturing Iodoform, Bromoform, and Ohloroform, (for which Letters Patent have been issued in Great Britain, No. 8,148, dated May 23, 1884, to myself; and to The Ghemische Fabrik auf Actien, Vorm. E. Schering, in the following countries; France, No. 162,306, dated May 23, 1884; Belgium, No. 65,227, dated May 23, 1884; Germany, No. 29,771, dated March 7, 1884; Luxemburg, N0. 405, dated May 24, 1884; Austria-Hungary, No. 19,725 and No. 42,228, dated September 23, 1884;) and I do hereby declare the fol lowing to be afull, clear, and exact description of the invention.
This invention relates to the production of iodoform, bromoform, and chloroform by electrolysis from the corresponding halogen combinations of the alkalies and alkaline earths in the presence of alcohol, aldehyde, or acetone and heat. If, for example, it is desired to obtain iodoform, I dissolve fifty kilograms of iodide of potassium in about three hundred kilograms ofwater, to which I add about thirty kilograms of alcohol of ninety-six per cent. This solution is then subjected to electrolysis in a suitable Vessel under a continuous introduction of carbonic acid and the application of heat. The iodoform obtained separates from the solution in a crystalline powder.
To obtain iodoform in large crystals, the iodide of potassium is dissolved in about twenty per cent. of alcohol, and subjected to the electrolysis described.
To produce bromoform or chloroform, the corresponding halogen combinations are subjected to electrolysis in the same manner as above described, except that no carbonicaoid is used.
In carrying out the above processes the carbonic dioxide employed in the production of 5 iodoform is introduced directly into the alcoholic solution of iodide of potassium, and simultaneously with the electric current.
I have found that an electric current of the strength of about sixty amperes will be sufficient to effect the decomposition of the solution mentioned.
The duration of the action of the electric current upon the solutions will naturally de pend upon their volume, said solutions being subjected to the action of the electric current until complete decomposition has been effected.
In the production of iodoform an alcoholic solution of iodide of potassium of any desired degree of concentration may be employed, the iodoform being separated from the alkali carbonate in the lye by simple filtration.
The chloroform or bromoform developed during the decomposition of the respective chloride or bromide solutions i. 6., their respective halogen combinationsis continuously distilled from the decomposing cell as it is developed.
Having now described my invention, what I claim is- The herein-described process of obtaining iodoform, bromoform, and chloroform, which consists in subjecting the corresponding halogen combinations of the alkalies or alkaline earths to electrolysis in the presence of alcohol, aldehyde, or acetone and heat, and with or without the addition of carbonic acid.
In testimony whereof I affix my signature in presence of two witnesses.
THEODOR KitMrF.
Witnesses l3. ROI, A. Dmmmus.
Publications (1)
Publication Number | Publication Date |
---|---|
US322940A true US322940A (en) | 1885-07-28 |
Family
ID=2392073
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US322940D Expired - Lifetime US322940A (en) | Theodor kempf |
Country Status (1)
Country | Link |
---|---|
US (1) | US322940A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3385775A (en) * | 1963-10-28 | 1968-05-28 | Ici Ltd | Production of halogenated organic compounds in fused electrolyte |
US20050230383A1 (en) * | 2004-03-01 | 2005-10-20 | Kraft Foods Holdings, Inc. | Multi-purpose food preparation kit |
-
0
- US US322940D patent/US322940A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3385775A (en) * | 1963-10-28 | 1968-05-28 | Ici Ltd | Production of halogenated organic compounds in fused electrolyte |
US20050230383A1 (en) * | 2004-03-01 | 2005-10-20 | Kraft Foods Holdings, Inc. | Multi-purpose food preparation kit |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US322940A (en) | Theodor kempf | |
DE2455890A1 (en) | PROCESS FOR THE PRODUCTION OF CALCIUM HYPOCHLORITE AND CRYSTALLINE SODIUM CHLORIDE | |
EP0439636A1 (en) | Alkali metal (hydrogen) carbonate production process | |
US1709297A (en) | Process of preparing maleic and succinic acid from furfural by electrolysis | |
DE2943360A1 (en) | METHOD FOR PRODUCING P-AMINOPHENOL | |
GB487009A (en) | Process for obtaining high standard and easily filtered calcium hypochlorite | |
US1062016A (en) | Process of precipitating ulmic compounds from the black liquors of soda pulp-mills. | |
CN105622702B (en) | A kind of preparation method of CDB-2914 key intermediate | |
US1408364A (en) | Manufacture of perborates | |
US1895414A (en) | Separation of ketoses from mixtures | |
US572345A (en) | Henry t | |
US568741A (en) | Henry r | |
US975613A (en) | Process of purifying chlorates. | |
DE1911174B2 (en) | Process for the production of malononitrile | |
US2457933A (en) | Process for electrolytic reduction of pentionic acid lactones | |
EP0040331B1 (en) | Method of preparing diacetoketogulonic acid | |
US727026A (en) | Camphidin and method of preparing same. | |
DE558379C (en) | Process for the oxidation of aldoses | |
US610616A (en) | Ip a t ttxtt | |
US602646A (en) | Officex | |
Sakurai | Electrolytic Reduction of Isatin and Its Derivatives. I. Reduction of Isatin | |
SU608763A1 (en) | Method of obtaining purified sodium bicarbonate | |
US576494A (en) | Adolf glaus | |
US2396570A (en) | Methods for purifying manganese in metal state | |
DE2021527A1 (en) | Process for obtaining pure manganese salts from manganese salt solutions containing organic impurities |