US1898688A - Purification of battery acid - Google Patents

Purification of battery acid Download PDF

Info

Publication number
US1898688A
US1898688A US56303631A US1898688A US 1898688 A US1898688 A US 1898688A US 56303631 A US56303631 A US 56303631A US 1898688 A US1898688 A US 1898688A
Authority
US
United States
Prior art keywords
acid
wood
battery
purification
activated carbon
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
Inventor
Clarence C Rose
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.)
Willard Storage Battery Co
Original Assignee
Willard Storage Battery Co
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 Willard Storage Battery Co filed Critical Willard Storage Battery Co
Priority to US56303631 priority Critical patent/US1898688A/en
Application granted granted Critical
Publication of US1898688A publication Critical patent/US1898688A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/54Reclaiming serviceable parts of waste accumulators
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00Sulfur; Compounds thereof
    • C01B17/69Sulfur trioxide; Sulfuric acid
    • C01B17/90Separation; Purification
    • C01B17/905Removal of organic impurities
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/84Recycling of batteries or fuel cells

Definitions

  • This invention relates to the purification of battery acid. It has to do primarily with the treatment of sulphuric acid employed in batteries during the original charging of the batteries, or the forming of the plates thereof.
  • the electrolyte thus used is generally of lower specific gravity than that normally employed in a fully charged battery. Hence, after it has performed its function, it is dumped from the battery and new acid of higher specific gravity is introduced in its place.
  • this dumped acid is contaminated more or less by wood acids, principally acetic acid, present to a small degree in the wood separators.
  • Such impure acid cannot be economically used a second time for the reason that the wood acids therein subject the positive plates of the battery to scaling and grid corrosion.
  • This action is very noticeable when acid containing more than .01% wood acid is used for the initial formation of a battery.
  • the amount of wood acids which the dumped electrolyte is likely to contain will depend upon the thoroughness with which the wood separators have been treated before they are used. In almost every case, however, the wood acid content of this electrolyte is found to be more than .01% and is genqe rally in the neighborhood of .03% or .04 0. dumped electrolyte a second time without dis astrons results.
  • 10 represents a relatively long tubular container of acid resisting material, into the bottom of which opens a pipe 11 for the admission of the impure acid, a valve 12 being employed for shutting off and controlling the rate of flow of the acid, it being understood that the acid is to be fed through the apparatus under pressure engendered by a pump or gravity resulting from the elevation of the acid tank with respect to the apparatus in question.
  • a second pipe 13 also makes connection with the lower end of container 10, this pipe having a shut-oil valve 14, and being employed for carrying off the impurities absorbed by the carbon.
  • a grid 15 upon which is supported a small quantity of coke 16 that is employed for holding the finer activated carbon .17. enclosed by the tubular container.
  • height and diameter of the container 10 are dependent upon the rate of fiow of the acid therethrough, it being necessary to maintain the acid in contact with the carbon for a given length of time.
  • a second grid 18 to prevent the carbon from being carried oil with the outgoing acid.
  • a draw-off pipe 19 in which is mounted a valve 20.
  • a connection to a steam pipe 21 At the top of the container 10 there is a connection to a steam pipe 21.
  • the process is to be started, the Valve 14 is closed and the valves 12 and 20 are opened, the valve 12 being opened partway only, if desired, so as to control the rate of flow of the acid into the container 10.
  • the coke 16 in addition to supporting the finer carbon 17, acts as a filter to remove any solid material which may have gotten into the battery acid. The latter then flows gradually upward through the activated carbon 17 and the wood acid is absorbed thereby, the filtrate which passes off through the grid 18 and pipe 19 being pure, or substantially pure, sulphuric acid capable of being used again in the formation of new batteries.
  • the acid may be used indefinitely when it is purified by my method after each forming operation.
  • valve 14 When the activated carbon has become saturated or so much so that the discharge is no longer of satisfactory purity, the percolation is stopped by the closing of valve 12. Valve 14 is then opened and the acid in the container permitted to drain ofi'. Then the valve 20 is closed and steam is introduced through pipe 21 and forced through the activated carbon and out through waste pipe 13. The carbon is thereby heated and the acid previously absorbed is driven off as a vapor, it being carried out through the waste pipe with the exhaust steam. When this cleaning operation has been continued a suliicient length of time, determined by test, the steam is turned off, the valve 14 closed, and the valves 12 and 20 opened for the resumption of the acid purifying process.

Description

Feb. 21, 1933.' c c ROSE 1,898,688
PURIFICATION OF BATTERY ACID Filed Sept. 16, 1951 STEAM ACT VA TED CA R80 N i FILTRATE ,Erz verz for" f m MMT7 Patented Feb. 21, 1933 UNITED STATES PATENT OFFICE CLARENCE G. ROSE, OF CLEVELAND, OHIO, ASSIGNOR TO WILLARD STORAGE BATTERY COMPANY, OF CLEVELAND, OHIO, A CORPORATION OF WEST VIRGINIA PURIFICATION OF BATTERY ACID Application filed September 16, 1931.
This invention relates to the purification of battery acid. It has to do primarily with the treatment of sulphuric acid employed in batteries during the original charging of the batteries, or the forming of the plates thereof. The electrolyte thus used is generally of lower specific gravity than that normally employed in a fully charged battery. Hence, after it has performed its function, it is dumped from the battery and new acid of higher specific gravity is introduced in its place.
If wood separators are employed in the battery, this dumped acid is contaminated more or less by wood acids, principally acetic acid, present to a small degree in the wood separators. Such impure acid cannot be economically used a second time for the reason that the wood acids therein subject the positive plates of the battery to scaling and grid corrosion. This action is very noticeable when acid containing more than .01% wood acid is used for the initial formation of a battery. The amount of wood acids which the dumped electrolyte is likely to contain will depend upon the thoroughness with which the wood separators have been treated before they are used. In almost every case, however, the wood acid content of this electrolyte is found to be more than .01% and is genqe rally in the neighborhood of .03% or .04 0. dumped electrolyte a second time without dis astrons results.
Prior to the present invention, the only method known for removing these wood acids from the battery acid involved boiling the impure acid down to a high acid concentration and then aerating it with compressed air, which is an expensive and troublesome process. After considerable experimentation, I have discovered that the removal of the wood acids may be effected directly, that V is, without boiling down, by the simple ex- Hence it is impossible to use such Serial No. 563,036.
means which I prefer to employ is that illustrated more or less diagrammatically in the accompanying drawing, the single figure of which is an elevational view of the apparatus,
with some parts broken away to more clearly illustrate the invention.
In the drawing, 10 represents a relatively long tubular container of acid resisting material, into the bottom of which opens a pipe 11 for the admission of the impure acid, a valve 12 being employed for shutting off and controlling the rate of flow of the acid, it being understood that the acid is to be fed through the apparatus under pressure engendered by a pump or gravity resulting from the elevation of the acid tank with respect to the apparatus in question. A second pipe 13 also makes connection with the lower end of container 10, this pipe having a shut-oil valve 14, and being employed for carrying off the impurities absorbed by the carbon.
Just above the bottom of the container 10 there is mounted a grid 15 upon which is supported a small quantity of coke 16 that is employed for holding the finer activated carbon .17. enclosed by the tubular container. The
height and diameter of the container 10 are dependent upon the rate of fiow of the acid therethrough, it being necessary to maintain the acid in contact with the carbon for a given length of time.
Near the upper end of container 10 I mount a second grid 18 to prevent the carbon from being carried oil with the outgoing acid. Just above this grid there is a draw-off pipe 19 in which is mounted a valve 20. At the top of the container 10 there is a connection to a steam pipe 21.
- lVhen the process is to be started, the Valve 14 is closed and the valves 12 and 20 are opened, the valve 12 being opened partway only, if desired, so as to control the rate of flow of the acid into the container 10. The coke 16, in addition to supporting the finer carbon 17, acts as a filter to remove any solid material which may have gotten into the battery acid. The latter then flows gradually upward through the activated carbon 17 and the wood acid is absorbed thereby, the filtrate which passes off through the grid 18 and pipe 19 being pure, or substantially pure, sulphuric acid capable of being used again in the formation of new batteries. In fact the acid may be used indefinitely when it is purified by my method after each forming operation.
When the activated carbon has become saturated or so much so that the discharge is no longer of satisfactory purity, the percolation is stopped by the closing of valve 12. Valve 14 is then opened and the acid in the container permitted to drain ofi'. Then the valve 20 is closed and steam is introduced through pipe 21 and forced through the activated carbon and out through waste pipe 13. The carbon is thereby heated and the acid previously absorbed is driven off as a vapor, it being carried out through the waste pipe with the exhaust steam. When this cleaning operation has been continued a suliicient length of time, determined by test, the steam is turned off, the valve 14 closed, and the valves 12 and 20 opened for the resumption of the acid purifying process.
In the foregoing description, I have necessarily gone somewhat into detail in order to explain fully the particular embodiments of the invention herein illustrated, but I desire it to be understood that such detail disclosure is not to be construed as amounting to a limitation, except as it may be included in the appended claims.
Having thus described my invention, I claim:
1. The method of separating wood acid impurities from sulphuric acid, which consists in bringing the impure acid into contact with activated carbon.
2. The method of separating acetic acid impurities from sulphuric acid, which consists in bringing the impure acid into contact with activated carbon.
3. The method of reclaiming sulphuric acid from battery acid adulterated with wood acids, which consists in bringing the impure acid into contact with activated carbon, and maintaining the contact a sufiicient length of time for the removal of the wood acids by the carbon.
at. The method of removing wood acid impurities from sulphuric acid, which consists in passing the impure acid through activated carbon.
5. The method of removing wood acid impurities from sulphuric acid employed in bat-- tery formation, which consists in passing the impure acid upwardly through a column'of activated carbon.
6. The method of removing wood acid impurities from sulphuric acid employed in battery formation, which consists in passing the impure acid upwardly through a column of granular activated carbon.
7. The method of removing wood acid impurities from sulphuric acid employed in battery formation, which consists in bringing signature.
CLARENCE C. ROSE.
US56303631 1931-09-16 1931-09-16 Purification of battery acid Expired - Lifetime US1898688A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US56303631 US1898688A (en) 1931-09-16 1931-09-16 Purification of battery acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US56303631 US1898688A (en) 1931-09-16 1931-09-16 Purification of battery acid

Publications (1)

Publication Number Publication Date
US1898688A true US1898688A (en) 1933-02-21

Family

ID=24248839

Family Applications (1)

Application Number Title Priority Date Filing Date
US56303631 Expired - Lifetime US1898688A (en) 1931-09-16 1931-09-16 Purification of battery acid

Country Status (1)

Country Link
US (1) US1898688A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2474170A (en) * 1943-07-27 1949-06-21 Butacet Ltd Separation of acetone and butyl alcohol from fermented mash by activated charcoal
US2985665A (en) * 1956-10-03 1961-05-23 Pittsburgh Chemical Company Purification of phthalic anhydride
WO2016160684A1 (en) * 2015-03-31 2016-10-06 Rohm And Haas Company Treating sulfuric acid
US10428163B2 (en) 2015-03-31 2019-10-01 Rohm And Haas Company Sulfonation process

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2474170A (en) * 1943-07-27 1949-06-21 Butacet Ltd Separation of acetone and butyl alcohol from fermented mash by activated charcoal
US2985665A (en) * 1956-10-03 1961-05-23 Pittsburgh Chemical Company Purification of phthalic anhydride
WO2016160684A1 (en) * 2015-03-31 2016-10-06 Rohm And Haas Company Treating sulfuric acid
KR20170133385A (en) * 2015-03-31 2017-12-05 롬 앤드 하아스 컴패니 Sulfuric acid treatment
US10138124B2 (en) 2015-03-31 2018-11-27 Rohm And Haas Company Treating sulfuric acid
US10428163B2 (en) 2015-03-31 2019-10-01 Rohm And Haas Company Sulfonation process

Similar Documents

Publication Publication Date Title
US3389079A (en) Water purification by capillary diffusion
US2729543A (en) Removal of sulfur dioxide from gases containing the same
US1898688A (en) Purification of battery acid
US3897331A (en) Mercury recovery
CN207632753U (en) A kind of biogas polishing purification compressed filling all-in-one machine
US1595683A (en) Process for extracting vapors from gaseous mixtures
CN104479848B (en) A kind of method that waste oil is environmental friendly regenerated
CN104229757B (en) A kind of method of dirty acid purification being processed to Returning process recycling
US1868581A (en) Method of revivifying adsorbents
CN111825058A (en) Germane preparation method and device based on automatic activation of molecular sieve
CN103285734B (en) A treatment process and a system for waste organic solvents based on nano filter membranes
US2901324A (en) Oil seal for electro-precipitators employed in carbon black processes
CN204121826U (en) More medium filter
CN115676781A (en) System and method for treating sulfur foam
GB124551A (en) Apparatus for Recovering Waste Oils or Separating Oil from Water or other Impurities.
DE10359959B9 (en) Dehumidification of biogas
CN206853404U (en) One kind failure selexol process regenerative device of solution
US3097157A (en) Oil purification process
JPWO2003072275A1 (en) Wet processing method for petroleum combustion ash
US1384978A (en) Process for reclaiming sludge acid in petroleum refining
CN110846085A (en) Cleaning technology and device for electrical tar precipitator
CN210683395U (en) Sewage filtering device for oil field exploitation
DE102013202960A1 (en) Method for separating silicon and polyethylene glycol from suspension during manufacturing of wafer for solar cell in photovoltaic industry, involves adding gas bubbles to particle of group such that particle of another group is deposited
CN215626798U (en) Processing system of sulphur foam
US1484258A (en) Process for the treatment of coal