US775752A - Manufacture of barium hydrate. - Google Patents

Manufacture of barium hydrate. Download PDF

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Publication number
US775752A
US775752A US17216703A US1903172167A US775752A US 775752 A US775752 A US 775752A US 17216703 A US17216703 A US 17216703A US 1903172167 A US1903172167 A US 1903172167A US 775752 A US775752 A US 775752A
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anode
hydrate
barium
compartment
cathode
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US17216703A
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Fredrik Jahn
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Harrison Bros & Co Inc
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Harrison Bros & Co Inc
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B4/00Electrothermal treatment of ores or metallurgical products for obtaining metals or alloys

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  • WITNESSES I la ZM zza a UNITED STATES Patented November 22, 1904.
  • the object of my invention is to'obtain barium hydrate by the electrolytic decomposition of barium sulfid. I accomplish this by electrolyzing a solution of barium sulfid in a 5 cell of which the anode-plate is very much larger than the cathode-plate and with the interposition of a porous diaphragm, whereby the cell is divided into an anode and cathode compartment. the formation of hydrate being chiefly effected in the former compartment.
  • Figure 1 represents a plan view
  • Fig. 2 a central longitudinal section, of such a cell.
  • the cell A which maybe a vessel of iron 3 or other suitable material, is furnished with a lining a, of insulating material, such as cement, and is preferably divided into three compartments by the porous partitions B B.
  • the respective electrodes which are preferably iron plates, are suspended from insulating cross bars 0 c.
  • the relative size of the electrodes plays an important part in the process and that the anode-plate should have a much 4 larger surface than the cathode-plate. Good results are obtained by using an anode which is about four times-as large as the cathode.
  • Within the cathode-compartment is suspended a small cathode-plate a, while within the anode-comparting at least twice the area of the cathode.
  • the sulfur that is precipitated at the anode is redissolved by the sulfid liquor with formation of polysulfids until the whole of the sulfid is thus converted. When this has occurred, there- 7 after the sulfur is precipitated and not redissolved.
  • the anode liquor contains from seventy-five to eighty per cent. of the dissolved barium as hydrate, the electrolysis is stopped.
  • I claim 1 The process of obtaining barium hydrate which consists in electrolyzing a strong solution of barium sullid in an anode-compartment, which is separated from its corresponding cathode-compartment by a porous partition, and with employment of a large anode and a small cathode, whereby there is obtained in said anode-compartment barium hydrate and thereafter separating l anode-compartment; and thereafter recovering the hydrate from the solution in the latter compartment, substantially as described.

Description

PATENTED NOV. 22, 1904.
F. JAHN.
MANUFACTURE OF BARIUM HYDRATE.
APPLICATION FILED SBPT.5, 1903.
N0, MODEL. 4
FIG. 1.
HGZ
WITNESSES: I la ZM zza a UNITED STATES Patented November 22, 1904.
PATENT OTFTQE.
FREDRIK JAHN, OF RIDLEY PARK, PENNSYLVANIA, ASSIGNOR TO HAR- RISON BROS. & 00.,
INCORPORATED, OF PHILADELPHIA, PENNSYL- VANIA, A CORPORATION OF PENNSYLVANIA.
.SPEOIFIGATION forming part of Letters Patent No. 775,752, dated November 22, 1904.
Application filed September 5, 1903.
To all whom it may concern.-
Be it known that I, FREDRIK J AHN, a subject of the King of Sweden and Norway, now residing at No. 36 Ridley avenue, Ridley Park,
Delaware county, and State of Pennsylvania,
have invented a certain new and useful Process for the Manufacture of Barium Hydrate, whereof the following is a specification, reference being had to the accompanying draw- 1ngs. a
The object of my invention is to'obtain barium hydrate by the electrolytic decomposition of barium sulfid. I accomplish this by electrolyzing a solution of barium sulfid in a 5 cell of which the anode-plate is very much larger than the cathode-plate and with the interposition of a porous diaphragm, whereby the cell is divided into an anode and cathode compartment. the formation of hydrate being chiefly effected in the former compartment.
My process is not dependent upon any particular form of apparatus; but I have illustrated in the drawings and will describe a conveniently-arranged apparatus in which my 5 invention may be practiced.
In said drawings, Figure 1 represents a plan view, and Fig. 2 a central longitudinal section, of such a cell.
The cell A, which maybe a vessel of iron 3 or other suitable material, is furnished with a lining a, of insulating material, such as cement, and is preferably divided into three compartments by the porous partitions B B.
Within these compartments the respective electrodes, which are preferably iron plates, are suspended from insulating cross bars 0 c. I have found that the relative size of the electrodes plays an important part in the process and that the anode-plate should have a much 4 larger surface than the cathode-plate. Good results are obtained by using an anode which is about four times-as large as the cathode. To provide for this, it is convenient to employ the two end compartments D D as anodecompartments and the central compartment E as cathode-compartments. Within the cathode-compartment is suspended a small cathode-plate a, while within the anode-comparting at least twice the area of the cathode.
tained by crystallization.
Serial No. 172,167. (No specimens.)
ment are suspended two anodes cl (Z, each hav- Into the anode compartment or compartments I introduce a strong solution of sulfid of barium, (say about thirty-five per cent.,) and into the cathode-compartment I introduce a weak solution of barium hydrate. It is desirable to cover the surfaces of the solutions with a thin layer of coal-oil to exclude the air. The current density should be rather highsay nine to fifteen amperes per square foot of anode-surface and forty to seventy 6O amperes per square foot of cathode-surface. As a result of theelectrolytic process set up by the current sulfur is precipitated at the anode in an insoluble state, thereby converting the barium sulfid into barium hydrate.
At the beginning of the process the sulfur that is precipitated at the anode is redissolved by the sulfid liquor with formation of polysulfids until the whole of the sulfid is thus converted. When this has occurred, there- 7 after the sulfur is precipitated and not redissolved. When the anode liquor contains from seventy-five to eighty per cent. of the dissolved barium as hydrate, the electrolysis is stopped.
By using electrodes of which the relative sizes are about as above specified I find that about thirty per cent. of the hydrate which is formed may be obtained from the cathodecompartment in a very pure state, the other seventy per cent. of the hydrate being at the anode. From the anode liquor containing sulfur as polysulfids the hydrate is readily ob- The precipitated sulfur may also be obtained from the anode- 5 compartment and be utilized.
Having thus described my invention, I claim 1. The process of obtaining barium hydrate which consists in electrolyzing a strong solution of barium sullid in an anode-compartment, which is separated from its corresponding cathode-compartment by a porous partition, and with employment of a large anode and a small cathode, whereby there is obtained in said anode-compartment barium hydrate and thereafter separating l anode-compartment; and thereafter recovering the hydrate from the solution in the latter compartment, substantially as described.
In testimony whereof I have signed my name to this specification, this 28th day of August, A. D. 1903, in the presence of two subscribing Witnesses.
FREDRIK J AHN Witnesses:
JAMEs H. BELL, M. K. TRUMBORE.
US17216703A 1903-09-05 1903-09-05 Manufacture of barium hydrate. Expired - Lifetime US775752A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3325382A (en) * 1962-03-01 1967-06-13 Pullman Inc Process for electrolysis of alkaline earth metal compounds in a mercury cell
US3361653A (en) * 1963-11-04 1968-01-02 Hooker Chemical Corp Organic electrolytic reactions
US3361656A (en) * 1966-05-16 1968-01-02 Hooker Chemical Corp Wicking electrode for an electrolytic cell

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3325382A (en) * 1962-03-01 1967-06-13 Pullman Inc Process for electrolysis of alkaline earth metal compounds in a mercury cell
US3361653A (en) * 1963-11-04 1968-01-02 Hooker Chemical Corp Organic electrolytic reactions
US3361656A (en) * 1966-05-16 1968-01-02 Hooker Chemical Corp Wicking electrode for an electrolytic cell

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