US1491498A - Method of electrolysis - Google Patents
Method of electrolysis Download PDFInfo
- Publication number
- US1491498A US1491498A US435153A US43515321A US1491498A US 1491498 A US1491498 A US 1491498A US 435153 A US435153 A US 435153A US 43515321 A US43515321 A US 43515321A US 1491498 A US1491498 A US 1491498A
- Authority
- US
- United States
- Prior art keywords
- anode
- electrolysis
- current
- approximating
- amperes
- 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
- 238000005868 electrolysis reaction Methods 0.000 title description 14
- 238000000034 method Methods 0.000 title description 9
- 239000000243 solution Substances 0.000 description 15
- 239000002253 acid Substances 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 6
- 235000011149 sulphuric acid Nutrition 0.000 description 6
- 239000001117 sulphuric acid Substances 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000003792 electrolyte Substances 0.000 description 5
- 239000010941 cobalt Substances 0.000 description 4
- 229910017052 cobalt Inorganic materials 0.000 description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
- 229910052787 antimony Inorganic materials 0.000 description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 3
- 235000009529 zinc sulphate Nutrition 0.000 description 3
- 239000011686 zinc sulphate Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000010405 anode material Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
- C25C7/06—Operating or servicing
Definitions
- the object of this invention is to provide means whereby the above mentioned disadvantages can be obviated without the neces sity of mechanical cleaning of'th e anodes by hammering or scraping which is the method usually used.
- this effect may be accomplished by making use of the expansive. effect of the bubbles of gas liberated at the surface of anelectrode during electrolysis. By so arranging the conditions that bubbles of gas are liberated behind the scale at the true anode surface, the scale is'broken oif and the.
- a solution of suitably hi h conductivity is one containing a considera le percentage of free acid, for example 10% or more.
- the density of current at the anode should be 50 amperes per square foot or 'higher.
- free acid concentration in the electrolyte may I conveniently be 250 grams of sulphuric acid per litre and the current density at the anode 100 amperes per square foot.- It. is understood that these figures are given merely in to their use.
Landscapes
- Chemical & Material Sciences (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 Apn 22, 1924.
UNITED STATES PATENT OFFICE.
UBYLN CLIFTON minimum, of JOHANNESBURG, TRANSVAAL, soo'rn AFRICA.
METHOD OF ELECTROLYSIS.
No Drawing.
In the electrolysis of aqueous solutions with insoluble anodes it frequently happens that incrustations or insoluble deposits are formed over the active surface of the anode which is in contact with the electrolyte; Such deposits or incrustations are frequently a source of serious trouble, causing as theydo the intervention of a poorly conducting medium between the anode and the electrolyte and thus raising the ohmic resistance of the circuit. Moreover, since these deposits possess usually a lower overvoltage than the anode material itself it sometimes happens that desirable reactions which depend for their continuance upon the maintenance of a high overvoltage are interfered with or even completely inhibited.
As an example of the conditions above described we may take the case of the electrolysis of solutions derived from the leaching of zinc ores with sulphuric acid. These solutions, after the ordinary processes of purification have been carried out, usually con-- ried out with an anode of lead or lead perox ide, all of the three metals in question are precipitated as insoluble oxidesin the vicinthe further precipitation of the oxides of manganese, cobalt and antimony is thus prevented. Moreover, since the resistance of this layer of scale is considerable, a substanillustration Application filed January 5, 1921. Serial No. 435,158.
tially higher voltage must be employed with consequent lossof power.
The object of this invention is to provide means whereby the above mentioned disadvantages can be obviated without the neces sity of mechanical cleaning of'th e anodes by hammering or scraping which is the method usually used. Accordin to the present invention, this effect may be accomplished by making use of the expansive. effect of the bubbles of gas liberated at the surface of anelectrode during electrolysis. By so arranging the conditions that bubbles of gas are liberated behind the scale at the true anode surface, the scale is'broken oif and the.
anodes thus kept continuously in good condition.
In order to attain this result it is necessary, firstly, to surround the anode with a solution of high electrical conductivity. Since the adhering scale is always to some extent porous the electrolyte will permeate it and come in contact with the anodejsurface beneath. Secondly, there must be employed a current of great intensity in proportion to the area .of the anode surface.
If these twoconditions are carried out it is found that the evolution of gas occurs not only at the surface-of the scale but also to i some extent behind it, with the result that the adhering scale is detached and falls away leaving the anode surface clean.
A solution of suitably hi h conductivity is one containing a considera le percentage of free acid, for example 10% or more. The density of current at the anode should be 50 amperes per square foot or 'higher.- As an example-of the application of the invention to the case. mentloned above. That of the electrolysis of zinc sulphate solutions, the
free acid concentration in the electrolyte may I conveniently be 250 grams of sulphuric acid per litre and the current density at the anode 100 amperes per square foot.- It. is understood that these figures are given merely in to their use.
- These conditions may be applied intermittently 'in order to. remove .adhering scale which has formed, or they. may be used continuously and the anode thus kept permanently .clean. The latter case is preferable since the ohmic resistance of the'circuit is thus'kept low and, moreover, objectionable constituents of the electrolyte such as antiand the invention is not limited Q mony, cobalt and manganese are continuously precipitated and removed from solution. 7
Having thus described my invention, what I claim and desire to secure by Letters Patcurrent of high density in proportion to its tion containing a acld content approximating 100 surface the currentdensity approximating 5O amperes or more per square foot of anode surface immersed. 2. In the electrolysis of zinc sulphate solutions with insoluble anodes, surrounding the anode with a solution containing a high percentage of free sulphuric acid, the rams or more of free acid per litre, and t e simultaneous ap lication to the anode of a current of big densit in proportion to its surface, the current ensity approximating 50 amperes or more per square foot of anode surface immersed.
3. In the electrolysis of aqueous solutions containing manganese, a method of keeping the anode free of encrustations, which consists in surroundingl the anode with a soluigh percentage of free acid, the acid content approximating 10 per cent, or more, and the simultaneous a plication to the anode of a current of high ensity in proportion to its surface, the current density approximating 5O amperes or more per square foot of anode surface immersed.
' 4. In the electrolysis of aqueous solutions containing manganese, a method of removing encrustations formed'on the anode surfaces, which consists in intermittentl surrounding the anode with a solution 0 high menace electrical conductivity, and simultaneously applying to the anode a current of high density in proportion to its surface, the current density approximatin 50 amperes or more per square foot of ano e surface immersed.
5. In the electrolysis of aqueous solutions containing manganese, antimony and cobalt a method of continuously precipitating said metals as insoluble oxides during the electrolysis of the-solution, which consists in surrounding the anode with a solution containing a high percentage of free sulphuric acid, the acid content approximating 100 grams or. more of free acid per litre, and simultaneously applying to the anode a current of high density in proportion to its surface,
the current density approximating 50 amperes or more per square foot'of anode surface immersed,
6. In the electrolysis of aqueous solutions containing manganese, antimony and cobalt, a method of continuousl precipitating said metals as insoluble oxi es during the electrolysis of the solution, which consists in surrounding the anode With a solution containing approximately 10 or cent or more of free sulphuric acid, an simultaneously applying to the anode a current of high density. approximating 5O amperes or more per square foot of submer ed surface".
7 In the electrolysis of zinc sulphate solutions containing manganese, a method of preventing encrustation of the anode, which consists in surrounding the anode with a solution containing a high percentage of free sulphuric acid, the acid content approximating 100 grams or more of free acid per litre, and simultaneously applying to the anode a current of high density 1n proportion to its surface, the current density approximating 50 amperes or more per square foot of anode surface immersed in the electrol te.
LYN CLIFTON T INTON.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US435153A US1491498A (en) | 1921-01-05 | 1921-01-05 | Method of electrolysis |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US435153A US1491498A (en) | 1921-01-05 | 1921-01-05 | Method of electrolysis |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1491498A true US1491498A (en) | 1924-04-22 |
Family
ID=23727216
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US435153A Expired - Lifetime US1491498A (en) | 1921-01-05 | 1921-01-05 | Method of electrolysis |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1491498A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3065155A (en) * | 1960-09-02 | 1962-11-20 | Manganese Chemicals Corp | Electrolytic manganese dioxide process |
-
1921
- 1921-01-05 US US435153A patent/US1491498A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3065155A (en) * | 1960-09-02 | 1962-11-20 | Manganese Chemicals Corp | Electrolytic manganese dioxide process |
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