US883651A - Electrolytic production of chromic acid. - Google Patents

Electrolytic production of chromic acid. Download PDF

Info

Publication number
US883651A
US883651A US29883306A US1906298833A US883651A US 883651 A US883651 A US 883651A US 29883306 A US29883306 A US 29883306A US 1906298833 A US1906298833 A US 1906298833A US 883651 A US883651 A US 883651A
Authority
US
United States
Prior art keywords
chromic acid
solution
acid
cell
cathode
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
Application number
US29883306A
Inventor
Max Le Blanc
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Priority to US29883306A priority Critical patent/US883651A/en
Application granted granted Critical
Publication of US883651A publication Critical patent/US883651A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G37/00Compounds of chromium
    • C01G37/02Oxides or hydrates thereof
    • C01G37/033Chromium trioxide; Chromic acid

Definitions

  • My invention relates to the electrolytic production of chromic acid by the oxidation of chromium compounds of a lower degree of oxidation, and in particular to the regeneration of chromic acid solutions which have been used for oxidizing purposes, for instance for the production of anthraquinone from anthracene.
  • I have devised a process and apparatus by means of which I can effect the continuous electrolytic production of chromic acid, allowing a solution of the chromium com ound which is to be oxidized to flow into tie apparatus and obtaining therefrom a solution of chromic acid.
  • an electro ytic cell in which the cathode and the anode are separated from each other by a wall which does not reach to the bottom of the cell, and the solution to be electrolyzed is introduced into the cell in such a manner that the cathode liquid alwa s contains'a sufficient quantity of acid to al ow the electrolysis to proceed properly.
  • This introduction can take lace in various ways, for example, the solution can be introduced continuously, or intermittently, .and either into the top of the cathode compartment, or as a horizontal layer at the bottom of the cell, preferably under the cathode com- This latter method is particu arly suitable if the solution to be electrolyzed artment.
  • the electrodes may be made of lead, or of any other suitable material, and can be of any convenient shape.
  • the wall which divides the anode from the cathode may be either pervious or impervious to electrolysis.
  • Figures 1 and 2 respectively represent a vertical cross-section and a plan of a cell of which the containing vessel 9 may be made of glass, wood, stone, or other suitable material; (1 represents the wall which separates the anode a from the cathode 7c, but which does not reach to the bottom of the said vessel.
  • the solution to be electrolyzed is introduced at 2 near to the bottom of the said vessel and the oxidized product flows out at b at the upper part of the other end of the said vessel.
  • the electrodes are made of hard lead.
  • the dimens'ions may be as foll0ws, for example.
  • the solution used can be prepared by dissolvin eighty (80) grams of chromium oxid (Cr Ofi in one (1) liter of twenty-four (24) per cent.
  • sulfuric acid and, on an average, seventeenv hundred and thirty (1730) cubic centimeters of this solution may be introduced into the contents can be about twenty-six (26) de-' grees centigrade.
  • the chromium in the solution After the apparatus has een in operation for about fourteen (14) days, the chromium in the solution will be found to be getting oxidized to a very satisfactory extent, while only a very little of the electric current supplied will'be wasted.

Description

'PATENTED MAR. 31, 1908.
M. L; BLANG. ELECTROLYTIC PRODUGTIONQF 01111019410 ACID.
APPLICATION FILED JL HL 31. 1906.
UNITED sTArnsPATENT OFFICE.
MAX LE BLANC, OF KARLSRUHE, GERMANY, ASSIGNOR TO BADISCHE ANILIN & SODA FABRIK, OF LUDWIGSHAFEN-ON-THE-RHINE, GERMANY, A CORPORATION.
ELECTROLYTIC PRODUCTION OF CHROMIC ACID.
Specification of Letters Patent.
Patented March 31, 1908.
Application filed January 31, 1906. Serial No. 298,833.
To all whom it may concern:
Be it known that I, l\dAX Ln BLANc, a subject of the Grand Duke of Baden, professor of chemistry and. doctor of philoso hy, residing at Karlsruhe, in the Grand Duc iy of Baden, GermanEmpire, have inventednew and useful Im rovements in the Electrolytic Production of Chromic Acid, of which the following is a specification.
My invention relates to the electrolytic production of chromic acid by the oxidation of chromium compounds of a lower degree of oxidation, and in particular to the regeneration of chromic acid solutions which have been used for oxidizing purposes, for instance for the production of anthraquinone from anthracene.
In the specifications of the German patents Nos. 103,860 of 1898to the Farl nverke Hochst and 117,949 of 1899 to Darmstadter are described methods for the electrolytic production of chromic acid and in each of these use is made of an electrolytic cell in which the anode and the cathode compartments are separated by a porous diaphragm.
I have devised a process and apparatus by means of which I can effect the continuous electrolytic production of chromic acid, allowing a solution of the chromium com ound which is to be oxidized to flow into tie apparatus and obtaining therefrom a solution of chromic acid.
In carrying out the recess according to my invention an electro ytic cell is employed in which the cathode and the anode are separated from each other by a wall which does not reach to the bottom of the cell, and the solution to be electrolyzed is introduced into the cell in such a manner that the cathode liquid alwa s contains'a sufficient quantity of acid to al ow the electrolysis to proceed properly. This introduction can take lace in various ways, for example, the solution can be introduced continuously, or intermittently, .and either into the top of the cathode compartment, or as a horizontal layer at the bottom of the cell, preferably under the cathode com- This latter method is particu arly suitable if the solution to be electrolyzed artment.
contains any chromic acid as otherwise such acid would tend to be reduced and cause loss of electric energy. When the solution is thus introduced at the bottom of the cell, the greater part of the cathode liquid does not take part in the circulation, but the loss of electrodes three (3) centimeters.
acid due to the movement of the ions does not exceed a definite amount, since a corresponding quantity of acid enters'by diffusion, or convection, from the lower layer of liquid. The electrodes may be made of lead, or of any other suitable material, and can be of any convenient shape. The wall which divides the anode from the cathode may be either pervious or impervious to electrolysis.
The best results are obtained when the solution to be electrolyzed approaches the anode at the points of greatest current density, afterwards passing to points of lower current density.
It must not be expected that good results will always be obtained immediately the apparatus is started working, since it is often only after a period, for instance fourteen days, of undisturbed working that the best results are shown. Y
\ The following is a description of a method of procedure'suitable for carrying out my invention, but the invention is not limited to this example.
Referring to the accompanying drawings, Figures 1 and 2 respectively represent a vertical cross-section and a plan of a cell of which the containing vessel 9 may be made of glass, wood, stone, or other suitable material; (1 represents the wall which separates the anode a from the cathode 7c, but which does not reach to the bottom of the said vessel. The solution to be electrolyzed is introduced at 2 near to the bottom of the said vessel and the oxidized product flows out at b at the upper part of the other end of the said vessel. The electrodes are made of hard lead. The dimens'ions may be as foll0ws, for example.
Length of cell forty (40) centimeters, width of cell fourteen (14) to fifteen (15) centimeters, depth of liquid seven (7) centimeters, length of cathode compartment thirty-five (35) centimeters, width of cathode compartment eight (8) to nine (9) centimeters, dis-' tance from the bottom of the cell of the wall (1 which separates the cathode and anode two (2) centimeters, distance of the electrodes from the bottom of the cell three (3) centimeters, length of electrodes thirty-four (34) to thirty-five (35) centimeters and height of The electrodes are placed only a few millimeters from the aforesaid separating wall (I. The solution used can be prepared by dissolvin eighty (80) grams of chromium oxid (Cr Ofi in one (1) liter of twenty-four (24) per cent.
sulfuric acid and, on an average, seventeenv hundred and thirty (1730) cubic centimeters of this solution may be introduced into the contents can be about twenty-six (26) de-' grees centigrade. After the apparatus has een in operation for about fourteen (14) days, the chromium in the solution will be found to be getting oxidized to a very satisfactory extent, while only a very little of the electric current supplied will'be wasted.
Now what I claim is: Y
.1. The process of making chromic acid continuously by electrolytically oxidizing a chromium compound of a lower degree of oxidation by treating an acid solution of the said chromium compound with an electric current while continuously passing the said solution into an electric cell in suc strength and quantity that 'the liquid treated at the cathode remains acid, all substantially as described.
2. The 'rocess of making chromic acid continuous y by electrolytically oxidizing a chromium compound of a lower degree of oxidation by treating an acid solution of the said chromium compound with an electric currentwhile continuously passing the said solution into an electric cell in such strength I and quantity that the liquid treated at the cathode remains acid and approaches the anode at the points of greatest current density afterwards passing to points of low r current density, all substantially as described.
In testimony whereof I have hereunto set 7 my hand in the presenceof two subscribing witnesses.
MAX LE BLANC.
Witnesses;
T. ALEG. LLOYD, ERNEST F. EHRHARDT'.
US29883306A 1906-01-31 1906-01-31 Electrolytic production of chromic acid. Expired - Lifetime US883651A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US29883306A US883651A (en) 1906-01-31 1906-01-31 Electrolytic production of chromic acid.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US29883306A US883651A (en) 1906-01-31 1906-01-31 Electrolytic production of chromic acid.

Publications (1)

Publication Number Publication Date
US883651A true US883651A (en) 1908-03-31

Family

ID=2952091

Family Applications (1)

Application Number Title Priority Date Filing Date
US29883306A Expired - Lifetime US883651A (en) 1906-01-31 1906-01-31 Electrolytic production of chromic acid.

Country Status (1)

Country Link
US (1) US883651A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3481851A (en) * 1964-10-29 1969-12-02 Lancy Lab Apparatus and procedure for reconditioning metal treating solutions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3481851A (en) * 1964-10-29 1969-12-02 Lancy Lab Apparatus and procedure for reconditioning metal treating solutions

Similar Documents

Publication Publication Date Title
US2921005A (en) Electrolytic conversions with permselective membranes
US3486992A (en) Process for electrolytic oxidation of thallium or cerium salts
US883651A (en) Electrolytic production of chromic acid.
US2232128A (en) Electrolysis of alkaline metal chlorides and apparatus therefor
Ramaswamy et al. Electrolytically Regenerated Ceric Sulfate for the Oxidation of Organic Compounds. I. Oxidation of p-Xylene to p-Tolualdehyde
US3833490A (en) Process for the preparation of 3,5-diiodo-4-hydroxybenzonitrile or 3-iodo-4-hydroxy-5-nitro-benzonitrile
US2843537A (en) Production of potassium permanganate
US2537304A (en) Electrolytic process and apparatus
US2285858A (en) Electrolytic process for the production of quinone and hydroquinone
US1322580A (en) Method and apparatus for producing quinone and quinol
US2984606A (en) Production of hydrous aluminas and aluminas
US2547231A (en) Electroosmotic isolation of streptomycin
US1788512A (en) Electrolysis
US591730A (en) Willy bein
US775752A (en) Manufacture of barium hydrate.
GB543294A (en) Electrolytic production of nickel
US975835A (en) Process of electrolytically treating tannic infusions of plants.
US1056118A (en) Method of electrolyzing streaming electrolytes.
US1837177A (en) Electrolytic process and apparatus
US683000A (en) Method of obtaining aluminium hydrate by electrolysis.
US1536569A (en) Impregnation of fibers by electrolysis
US1516326A (en) Manufacture of electrolytic iron
US1315546A (en) Method of preparation of acetic acid
US558052A (en) encke
US1258529A (en) Process and apparatus for producing alkali metals.