US825057A - Method of making sulfuric acid. - Google Patents
Method of making sulfuric acid. Download PDFInfo
- Publication number
- US825057A US825057A US17651103A US1903176511A US825057A US 825057 A US825057 A US 825057A US 17651103 A US17651103 A US 17651103A US 1903176511 A US1903176511 A US 1903176511A US 825057 A US825057 A US 825057A
- Authority
- US
- United States
- Prior art keywords
- sulfuric acid
- electrodes
- sulfur
- solution
- dioxid
- 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
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- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 title description 38
- 238000004519 manufacturing process Methods 0.000 title description 4
- 239000000243 solution Substances 0.000 description 20
- 229940032330 sulfuric acid Drugs 0.000 description 18
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 9
- 229910052717 sulfur Inorganic materials 0.000 description 9
- 229960005349 sulfur Drugs 0.000 description 9
- 235000001508 sulfur Nutrition 0.000 description 9
- 239000011593 sulfur Substances 0.000 description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 239000003792 electrolyte Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000011437 continuous method Methods 0.000 description 3
- 238000005868 electrolysis reaction Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000543381 Cliftonia monophylla Species 0.000 description 1
- -1 SULFURIO Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Images
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
- C25B1/22—Inorganic acids
Definitions
- This-invention is a method of making sulfuric acid by electrolytic oxidation of sulfur dioxid or sulfurous acid. It has heretofore been proposed to electrolytically oxidize sulfur dioxid, the gas being injected into the electrolyte through a carbon anode or in proximity to the anode. In such cases the reaction proceeds with separation of sulfur at the cathode, and it has been proposed to keep such separated sulfur from the anode by means of a diaphragm interposed between the electrodes.
- the sulfur dioxid is oxidized in an electrolytic cell or tank provided with anodes of lead, the electrodes being connected according to the series system-that is to say, in such manner that the intermediate or unconnected plates act as bipolar electrodes. Under these conditions the sulfur dioxid dissolved or otherwise retained in the bath is oxidized at the anodes to sulfuric acid.
- the cathode surfaces it is desirable to use a metal having. a low. cathode potential, whereb the cathodic separation of sulfur is reduce to a minimum.
- copper electrodeposited upon the cathode surfaces is preferred.
- Sulfuric-acid solution of about twent per cent. concentration is saturated with su fur dioxid by means of a coke-tower or other suitable device. This solution is then caused to flow through the electrolytic cell and past the electrodes therein, whereb the sulfur dioxid is oxidized to sulfuric aci and a solution is obtained which may approach thirty per cent.
- sulfur dioxid may also be inj ected into the electrolytic cell, and the temand so arran ed therein that t perature of the solution may be lowered to any desired extent to increase the quantity of sulfur dioxid held in solution therein.
- FIGs. 1 and 2 1 indicates a tank or containing vessel which may be constructed of cement, lead-lined wood, enameled iron, or other material substantially unafiected by the electrolyte.
- 2 3 4 represent electrodes disposed transversely of said tank e electrolyte is caused to ow alternately over and under the plates. It will be understood that the electrodes may "be otherwise arranged in the tank. For instance, lateral passages may be provided between the electrodes and the side of the tank or through the electrodes themselves in such manner as to direct the elec trolyte in a tortuous path, or any other suitable arrangement for causing the electrolyte to flow past the active surfaces of the electrodes may be used.
- the intermediate electrodes 3 have no metallicconnection with the circuit and accordin ly act as bipolar electrodes,- that face of each electrode late which is nearest the anode acting as acat ode, and the opposite face of each plate acting as an anode, as is well understood.
- the end electrodes 2 4 are the terminals of the electric circuit. Appropriate inlet and discharge passages 7 8 are provided for the solution. a
- the anode connection is-assumed to be made at plate 2 and said late is preferably formed of a sheet of lead Plate 4, to which the cathode connection is made, may consist of a sheet of copper or of lead faced with copper.
- the intermediate plates 3, of which an desired number are used, are in this em odiment of my invention formed of sheets of lead 5, having electrodeposited upon their cathode surfaces a layer of metallic copper 6, which, b reason of its low cathode potential in the so ution, serves to reduce the uantity of sulfur separated by cathodic re uction. While I consider this to be the preferred form I to, but may employ anode surfaces of platinum.
- the lead anode surfaces become eroxidized and the sulfur dioxid containe in the electrolyte becomes oxidized to sulfuric acid, said oxidation being probably effected, in part, at least, through the agency of the lead eroxid on the anodes.
- the injection of su fur dioxid into the bath serves to prevent the formation of persulfuric acid. Any traces of sulfur which may be formed are conveniently removed from the solution by boiling to coagulate the sulfur and subsequently filtering.
- the anode faces being composed of lead and the cathodef'aces of copper, substantially as described.
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Metals (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Description
PATENTED JULY 3, 1906.
W. McA. JOHNSON.
METHOD OF MAKING SULFURIO ACID.
APPLICATION FILED OCT. 10, 1903.
,-Z7u c ILCO r 7% Q, JAM;
muwsses v 63mm ad s UNITED STATES PATENT oFFIoE.
Specification of Letters Patent.
latented July 3, 1906.
Application filed October 10. 1903. Serial No. 176,611-
To all whom it may concern:
Be it known that I, WOOLSEY MoA. JOHN- SON, a citizen of the United States, residing at Iola, in the county of Allen and State of Kansas, have invented certain new and useful Improvements in Methods of Making Sulfuric Acid, of which the following is a specification.
This-invention is a method of making sulfuric acid by electrolytic oxidation of sulfur dioxid or sulfurous acid. It has heretofore been proposed to electrolytically oxidize sulfur dioxid, the gas being injected into the electrolyte through a carbon anode or in proximity to the anode. In such cases the reaction proceeds with separation of sulfur at the cathode, and it has been proposed to keep such separated sulfur from the anode by means of a diaphragm interposed between the electrodes.
According to the preferred embodiment of my invention the sulfur dioxid is oxidized in an electrolytic cell or tank provided with anodes of lead, the electrodes being connected according to the series system-that is to say, in such manner that the intermediate or unconnected plates act as bipolar electrodes. Under these conditions the sulfur dioxid dissolved or otherwise retained in the bath is oxidized at the anodes to sulfuric acid. For the cathode surfaces it is desirable to use a metal having. a low. cathode potential, whereb the cathodic separation of sulfur is reduce to a minimum. For this purpose copper electrodeposited upon the cathode surfaces is preferred.
My preferred procedure is as follows: Sulfuric-acid solution of about twent per cent. concentration is saturated with su fur dioxid by means of a coke-tower or other suitable device. This solution is then caused to flow through the electrolytic cell and past the electrodes therein, whereb the sulfur dioxid is oxidized to sulfuric aci and a solution is obtained which may approach thirty per cent.
. concentration. A certain proportion of said acid is withdrawn and concentrated or utilized in any desired manner, while the remaining portion, diluted withwater to twenty per cent. and again saturated with sulfur dioxid, is returned to the electrolytic cell, this cycle of operations being repeated indefinitely.
If desired, sulfur dioxid may also be inj ected into the electrolytic cell, and the temand so arran ed therein that t perature of the solution may be lowered to any desired extent to increase the quantity of sulfur dioxid held in solution therein.
For a clear understanding-of my invention reference is made to the accompanying drawings, wherein- F i ure 1 is a central longitudinal section of one orm of electrolytic cell suitable for the production of sulfuric acid according to my method. Fig. 2 is a plan view of the same, and Fig. 3 is a modification illustrating the use of electrodes whose anode and cathode faces are composed of dissimilar metals.
Referring to Figs. 1 and 2, 1 indicates a tank or containing vessel which may be constructed of cement, lead-lined wood, enameled iron, or other material substantially unafiected by the electrolyte. 2 3 4 represent electrodes disposed transversely of said tank e electrolyte is caused to ow alternately over and under the plates. It will be understood that the electrodes may "be otherwise arranged in the tank. For instance, lateral passages may be provided between the electrodes and the side of the tank or through the electrodes themselves in such manner as to direct the elec trolyte in a tortuous path, or any other suitable arrangement for causing the electrolyte to flow past the active surfaces of the electrodes may be used. The intermediate electrodes 3 have no metallicconnection with the circuit and accordin ly act as bipolar electrodes,- that face of each electrode late which is nearest the anode acting as acat ode, and the opposite face of each plate acting as an anode, as is well understood. The end electrodes 2 4 are the terminals of the electric circuit. Appropriate inlet and discharge passages 7 8 are provided for the solution. a
In the modification illustrated in Fig. 3 the anode connection is-assumed to be made at plate 2 and said late is preferably formed of a sheet of lead Plate 4, to which the cathode connection is made, may consist of a sheet of copper or of lead faced with copper. The intermediate plates 3, of which an desired number are used, are in this em odiment of my invention formed of sheets of lead 5, having electrodeposited upon their cathode surfaces a layer of metallic copper 6, which, b reason of its low cathode potential in the so ution, serves to reduce the uantity of sulfur separated by cathodic re uction. While I consider this to be the preferred form I to, but may employ anode surfaces of platinum.
In operation, the lead anode surfaces become eroxidized and the sulfur dioxid containe in the electrolyte becomes oxidized to sulfuric acid, said oxidation being probably effected, in part, at least, through the agency of the lead eroxid on the anodes. The injection of su fur dioxid into the bath, in addition to increasing the concentration of the product, serves to prevent the formation of persulfuric acid. Any traces of sulfur which may be formed are conveniently removed from the solution by boiling to coagulate the sulfur and subsequently filtering.
By the ex ression a solution containing sulfur dioxi as herein em loyed, I intend to include solutions in whic the sulfur dioxid may exist in combination, as solutions of sulfurous acid.
I claim 1. The herein-described method of producing sulfuric acid, which consists in electrolyzing a solution containing sulfur dioxid by means of electrodes electrically connected in series, the anode faces being com osed of lead and the cathode faces of a meta having a low cathode potential, substantially as described.
2. The herein-described method of producing sulfuric acid, which consists in electro;
lyzing a solution containing sulfur dioxid by means of electrodes electrically connected in series, the anode faces being composed of lead and the cathodef'aces of copper, substantially as described.
3. The herein-described method of producing sulfuric acid, which consists in electrolyzing a solution containing sulfur dioxid by means of electrodes electrically connected in series, the anode faces being composed of lead and the cathode faces of elee'trcsdepesited copper, substantially as described.
4. The herein described continuous method of making sulfuric acid, which consists in electrolyzin a solution of sulfuric acid containing sul ur dioxid, thereby increasing the concentration of the sulfuric acid in solution, withdrawing a portion of the solution, diluting the remaining portion, introducing thereinto further quantities of sul fur dioxid, and repeating the electrolysis, substantially as described.
5. The herein described continuous method of making sulfuric acid, which consists in electrolyzing a solution of sulfuric acid containing sulfur dioxid by means of electrodes electrically connected in series, thereby increasin the concentration of the sulfuric acid in so ution, withdrawing a portion of the solution, diluting the remaining portion, introducing thereinto further quan tities of sulfur dioxid, and repeating the electrolysis, substantially as described. I
6. The herein, described continuous method of making sulfuric acid, which con.- sists in electrolyzin a solution of sulfuric acid containing sull ur dioxid by means of electrodes electrically connected in series, the anode faces being composed of lead and the cathode faces of cop er, thereby increasin the concentration 0 the sulfuric acid in so ution, withdrawing a portion of the solution, dilutin the remaining portion, introducin therelnto further quantities of sulfur dioxi and repeatin the electrolysis, substantially as described.
In testimony whereof I affix my signature in presence of two witnesses.
WOOLSEY MoA. JOHNSON. Witnesses:
CHARLES M. STARKWEATHER, JOHN FELT MoRRIs.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17651103A US825057A (en) | 1903-10-10 | 1903-10-10 | Method of making sulfuric acid. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17651103A US825057A (en) | 1903-10-10 | 1903-10-10 | Method of making sulfuric acid. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US825057A true US825057A (en) | 1906-07-03 |
Family
ID=2893537
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US17651103A Expired - Lifetime US825057A (en) | 1903-10-10 | 1903-10-10 | Method of making sulfuric acid. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US825057A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2573788A (en) * | 1948-11-27 | 1951-11-06 | American Viscose Corp | Electrolytic cell |
| US2631973A (en) * | 1948-10-26 | 1953-03-17 | American Viscose Corp | Sulfuric acid recovery process |
| US4830718A (en) * | 1985-10-21 | 1989-05-16 | John Stauffer | Removal of sulfur dioxide (SO2) from waste gases and recovery as sulfuric acid |
| WO1990012753A1 (en) * | 1988-12-30 | 1990-11-01 | Stauffer John E | Removal of sulfur dioxide (so2) from waste gases and recovery as sulfuric acid |
-
1903
- 1903-10-10 US US17651103A patent/US825057A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2631973A (en) * | 1948-10-26 | 1953-03-17 | American Viscose Corp | Sulfuric acid recovery process |
| US2573788A (en) * | 1948-11-27 | 1951-11-06 | American Viscose Corp | Electrolytic cell |
| US4830718A (en) * | 1985-10-21 | 1989-05-16 | John Stauffer | Removal of sulfur dioxide (SO2) from waste gases and recovery as sulfuric acid |
| WO1990012753A1 (en) * | 1988-12-30 | 1990-11-01 | Stauffer John E | Removal of sulfur dioxide (so2) from waste gases and recovery as sulfuric acid |
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