US2527340A - Sodium bicarbonate production - Google Patents

Sodium bicarbonate production Download PDF

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US2527340A
US2527340A US736352A US73635247A US2527340A US 2527340 A US2527340 A US 2527340A US 736352 A US736352 A US 736352A US 73635247 A US73635247 A US 73635247A US 2527340 A US2527340 A US 2527340A
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Taylor John Ross
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RICHARD KELLOGG WURTELE
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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01DCOMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
    • C01D7/00Carbonates of sodium, potassium or alkali metals in general
    • C01D7/18Preparation by the ammonia-soda process

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  • This invention relates to the production of soda ash and isfparticularly directed to that portion of the method and apparatus in which sodium bicarbonate is precipitated by carbonating ammoniated brine liquor, which constitutes one stage inthe well known method of making soda ash.
  • the carloonaiting step is carried out in tall sectional cast iron towers, usually in the neighborhood of 75 feet high, divided into a large number of sections with means for gas distribution in each section.
  • the ammoniated brine is fed into the tower at the top and carbon dioxide is pumped in to the tower at the bottom under sufficient pressure to force it upwardly against the static head of the liquor.
  • Bef cause of scale formation and sedimentation the columns become dirty in a few days and have to be cleaned out. This requires maintenance of a plurality of columns or towers to permit continued operation while one is being cleaned. This adds substantially to the expense and because of the size and construction of the columns they are costly.
  • the carbon dioxide must be pumped through the liquor under a pressure of from 30 to 35 pounds per square inch in order to overcome the relatively high pressure of the static head of the liquor.
  • ammonium bicarbonate and sodium chloride will not'remain in equilibrium at l5 C. under atmospheric pressure, and'consequently sodium bicarbonate and ammonium chloride are formed.
  • the pressure involved, as affecting the equilibrium is the static pressure of the body of liquor plus the pressure of the gas upon the liquor. Since pressure and temperature must be mutually related, to promote efciency of sodium bicarbonate precipitation, the importance of operational control of both gas and static head pressure will be appreciated, and particularly since the heat generated is inherent in the reaction.
  • the high pressure necessary in the conventional apparatus and method of operation, as well as the cooling effect of an excessive quantity of CO2 makes it impossible to maintain the temperature-pressure equilibrium required for maximum bicarbonate precipitation, except in a restricted zone adjacent the liquid feed end of the apparatus.
  • the object of the present invention is to provide a method of and apparatus for carbonating the ammo-niated brine and precipitating sodium bicarbonate which is much more economical in installation as well as maintenance costs, which greatly reduces, sedimentation and scale formation, which reduces operating diiculties, which permits more continuity and efficiency of operation without the necessity of maintaining excessive quantities of liquor in the system and which avoids the necessity for installing and maintaining spare units.
  • the invention contemplates the provision of a plurality of relatively small chambers, prei"- erably cylindrical with a height equal to about twice the diameter, with agitation in each chamber to prevent sedimentation of sodium bicarbonate and means for circulating carbon dioxide under low pressure in and through the chambers.
  • Fig. l is a section elevation of one arrangement of the chambers
  • Figure 2 is a similar view of another arrangement of the chambers.
  • I represents a compartment or chamber, preferably cylindrical, a plurality of which are interconnected by means of a liquid conduit 2 leading from the bottom zone ofV one chamber to the next in the series.
  • 3 is a conduit for feeding ammoniated brine to the initial chamber of the carbonating unit.
  • a conduit 4 delivers carbon dioxide containing gas to the bottom of the last chamber of the Vseries and a pipe 6 leads from the upper portion of each cham# ber to discharge unabsorbed gas into the preced ing chamber of the series adjacent its bottom.
  • An agitating device 8 is provided in each chamber.
  • the discharge outlet 9 of the last chamber in the series leads to a filter I I disposed to maintain a constant level of liquor in the system.
  • a gas outlet Ill at the top of the initial chamber of the series leads to a scrubber not shown for the recovery of ammonia and carbon dioxide in the unabsorbed gas.
  • the agitating device 8 in each lchamber is carried by a shaft l2 driven by a pulley or the like I3, the series of which may be operatedfrom a common source of power
  • the arrangements shown in Figures 1 Aand 2 are the same except that in that of Figure 1 the chambers I are successively arranged on a lower level to facilitate gravity flow of the charge.
  • Low pressure pumps or gas blowers 5 in pipes 4, and 'l in pipes E, are provided to force the incoming gas down to the bottom of each chamber. These pumpsI are operated at speeds which pass the desired volume of gas into each of the chambers.
  • the CO2 is pumped into each vessel under a rela- :tively low pressure of :from 3, to 5 lbs. per square inch. Since the CO2 is constantly pumped out of each chamber, the effect is that the pressure in each chamber is substantially atmospheric, whereby optimum operating conditions are maintained in each chamber for the precipitation of bicarbonate.
  • a second gas line I4 delivers carbon dioxide from a lime kiln to augment the gas supply from line 4 and this line I4 is connected to any desired number of the individual gas lines 6 connecting successive chambers by means of pipes I with valves I6.
  • the line 4 preferably leads from a calciner not shown which liberates carbon dioxide from the sodium bicarbonate as soda ash is formed therein.
  • 'Ihe gas from the calciner normally has a higher carbon dioxide content than that from the lime kiln and it is best adapted for the final stages of the carbonation of the liquor. This method of providing a renewed supply of carbon dioxide insures maintenance of an efficient supply of CO2 to each reaction chamber.
  • the tanks are relatively short or 10W and are preferably made of welded plate or the like.
  • the construction is thus of light weight and does not cost more than substantially 25% of that of the conventional equipment.
  • the agi, tator in each chamber is arranged to prevent sedimentation or scale formation therein.
  • ammoniated brine is fed into the initial chamber through the conduit 3 and while continuously agitated this liquor flows through thefsuccessive chambers in counter current to carbon dioxide which progressively reacts therewithto form sodium bicarbonate.
  • the 4charge flows by gravity continuously through the several reaction chambers of the unit and is discharged therefrom under a pressure not greater than atmospheric.
  • the sodium bicarbonate crystals formed are carried in the liquor to the lter with little or no opportunity for sedimentation in the chambers.u Subjecting the owing liquor to the gradually increasing concentration of carbon dioxide gives control of the size of the sodium bicarbonate crystals formed.
  • the coarser crystals thus formed are filtered more readily and permit longer life of the lters because of the small proportion of iine crystals. They wash more readily with less water, hence less dilution of the filtrate and less liquor from which to recover ammonia.
  • the crystals carry less adhering water to be removed in the calciner and returned to the circuit with the gases.
  • the rate of feed automatically controls the liquor-level in each chamber by maintaining a static head pressure suicient to cause the'floW of the liquor.
  • each bicarbonate precipitation unit operates eiiiciently only 60% of the time because of the necessity of periodically removing sediment.
  • the unit may be operated eiciently at 10 to 100% of its capacity, thus permitting great flexibilty in production.
  • the usual commercial unit can be operated only at about 70 to 100% of its 4 capacity. Operating costs are not moreA than two-thirds of that of the conventional equipment.
  • Gas unabsorbed in its passage through the chambers is conveyed to scrubbers for the recovery of ammonia and carbon dioxide carried by it.
  • the mechanical agitation prevents sedimentation regardless of the particular rate of flow through the unit, thus the rate of flow may be adjusted for maximum efficiency of the conversion reaction to sodium bicarbonate and maintained there indenitely. This will x the rate of operation of the whole system and thereafter control of the brine feed to the scrubbers regulates the operation; this affords continuous operation at a uniform rate throughout the Whole plant and greatly increased efliciency over the method now used.
  • a cooling system of any desired type is preferably incorporated in the unit to remove the heat of reaction and to cool the liquor in the discharge end of the system to as low a temperature as possible, in order to facilitate maintenance of the temperature-pressure equilibrium at the optimum level indicated.
  • the cutting out of one or more of the chambers in a system may readily be accomplished by providing the necessary gas and liquor by-pass pipe lines, Thus, repairing of individual units may be carried out without disturbing the operation of the remainder of the system, and the number of units in use may be varied to meet requirements.
  • a method of producing sodium bicarbonate which comprises arranging a series of at least four bodies of ammoniated brine in horizontally disposed relation to each other in a series of reaction chambers, feeding ammoniated brine in to thelower portion of the rst of said series of reaction chambers, passing a gravity flow of brine from the bottom zone of each chamber except the last of the series into the bottom zone of the adjacent succeeding chamber of the series, withdrawing the brine from the lower zone of the last chamber of the series and discharging it at atmospheric pressure at a higher level below the tops of said chambers to maintain a constant level of brine in the chambers, and passing a stream of gas containing carbon dioxide successively through the bodies of brine in said series from the last to the first thereof to maintain a concentration of carbon dioxide in said bodies of gradually increasing degree from the first to the lastI thereof, said stream of gas being passed through the bodies by separately pumping the unabsorbed gas from each chamber excepting the first of the series at a gauge pressure of from about v3 to about 5 pounds through

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Description

0ct. 24, 1950 J. R. TAYLOR 2,527,340
SODIUM BICARBONATE PRODUCTION Filed March 21, 1947 i 7 6 /z Lg u 5. i l 0 s s g alla n, r I a l l n v 3j j@ Il) 3 T Patented Oct. n24, A 1950 2,523,340v SODIUM BICARBONATEPRODUCTION John Ross Taylor, Westmount, Quebec, Canada, assignor to Richard Kellogg Wurtele, Goderich,
Ontario, Canada Application March 21, 1947, serial No. 736,352 In Canada June 24, 1943 2 Claims'. 1
This invention relates to the production of soda ash and isfparticularly directed to that portion of the method and apparatus in which sodium bicarbonate is precipitated by carbonating ammoniated brine liquor, which constitutes one stage inthe well known method of making soda ash.
In the usual practice the carloonaiting step is carried out in tall sectional cast iron towers, usually in the neighborhood of 75 feet high, divided into a large number of sections with means for gas distribution in each section. The ammoniated brine is fed into the tower at the top and carbon dioxide is pumped in to the tower at the bottom under sufficient pressure to force it upwardly against the static head of the liquor. Bef cause of scale formation and sedimentation the columns become dirty in a few days and have to be cleaned out. This requires maintenance of a plurality of columns or towers to permit continued operation while one is being cleaned. This adds substantially to the expense and because of the size and construction of the columns they are costly.
The carbon dioxide must be pumped through the liquor under a pressure of from 30 to 35 pounds per square inch in order to overcome the relatively high pressure of the static head of the liquor. Upon application of the phase rule, itl is known that ammonium bicarbonate and sodium chloride will not'remain in equilibrium at l5 C. under atmospheric pressure, and'consequently sodium bicarbonate and ammonium chloride are formed. The pressure involved, as affecting the equilibrium, is the static pressure of the body of liquor plus the pressure of the gas upon the liquor. Since pressure and temperature must be mutually related, to promote efciency of sodium bicarbonate precipitation, the importance of operational control of both gas and static head pressure will be appreciated, and particularly since the heat generated is inherent in the reaction. The high pressure necessary in the conventional apparatus and method of operation, as well as the cooling effect of an excessive quantity of CO2, makes it impossible to maintain the temperature-pressure equilibrium required for maximum bicarbonate precipitation, except in a restricted zone adjacent the liquid feed end of the apparatus.
The object of the present invention is to provide a method of and apparatus for carbonating the ammo-niated brine and precipitating sodium bicarbonate which is much more economical in installation as well as maintenance costs, which greatly reduces, sedimentation and scale formation, which reduces operating diiculties, which permits more continuity and efficiency of operation without the necessity of maintaining excessive quantities of liquor in the system and which avoids the necessity for installing and maintaining spare units.
The invention contemplates the provision of a plurality of relatively small chambers, prei"- erably cylindrical with a height equal to about twice the diameter, with agitation in each chamber to prevent sedimentation of sodium bicarbonate and means for circulating carbon dioxide under low pressure in and through the chambers.
The invention will be described with reference tothe accompanying drawing which illustrates more or less diagrammatically the apparatus used, and in which Fig. l is a section elevation of one arrangement of the chambers, and
Figure 2 is a similar view of another arrangement of the chambers.
In the drawing I represents a compartment or chamber, preferably cylindrical, a plurality of which are interconnected by means of a liquid conduit 2 leading from the bottom zone ofV one chamber to the next in the series. 3 is a conduit for feeding ammoniated brine to the initial chamber of the carbonating unit. A conduit 4 delivers carbon dioxide containing gas to the bottom of the last chamber of the Vseries and a pipe 6 leads from the upper portion of each cham# ber to discharge unabsorbed gas into the preced ing chamber of the series adjacent its bottom. An agitating device 8 is provided in each chamber. The discharge outlet 9 of the last chamber in the series leads to a filter I I disposed to maintain a constant level of liquor in the system. A gas outlet Ill at the top of the initial chamber of the series leads to a scrubber not shown for the recovery of ammonia and carbon dioxide in the unabsorbed gas. The agitating device 8 in each lchamber is carried by a shaft l2 driven by a pulley or the like I3, the series of which may be operatedfrom a common source of power The arrangements shown in Figures 1 Aand 2 are the same except that in that of Figure 1 the chambers I are successively arranged on a lower level to facilitate gravity flow of the charge. Low pressure pumps or gas blowers 5 in pipes 4, and 'l in pipes E, are provided to force the incoming gas down to the bottom of each chamber. These pumpsI are operated at speeds which pass the desired volume of gas into each of the chambers. The CO2 is pumped into each vessel under a rela- :tively low pressure of :from 3, to 5 lbs. per square inch. Since the CO2 is constantly pumped out of each chamber, the effect is that the pressure in each chamber is substantially atmospheric, whereby optimum operating conditions are maintained in each chamber for the precipitation of bicarbonate.
As illustrated in Figure 2 a second gas line I4 delivers carbon dioxide from a lime kiln to augment the gas supply from line 4 and this line I4 is connected to any desired number of the individual gas lines 6 connecting successive chambers by means of pipes I with valves I6. The line 4 preferably leads from a calciner not shown which liberates carbon dioxide from the sodium bicarbonate as soda ash is formed therein. 'Ihe gas from the calciner normally has a higher carbon dioxide content than that from the lime kiln and it is best adapted for the final stages of the carbonation of the liquor. This method of providing a renewed supply of carbon dioxide insures maintenance of an efficient supply of CO2 to each reaction chamber.
As shown the tanks are relatively short or 10W and are preferably made of welded plate or the like. The construction is thus of light weight and does not cost more than substantially 25% of that of the conventional equipment. The agi, tator in each chamber is arranged to prevent sedimentation or scale formation therein.
In 'operation ammoniated brine is fed into the initial chamber through the conduit 3 and while continuously agitated this liquor flows through thefsuccessive chambers in counter current to carbon dioxide which progressively reacts therewithto form sodium bicarbonate. The 4charge flows by gravity continuously through the several reaction chambers of the unit and is discharged therefrom under a pressure not greater than atmospheric. Under the influence of the agitators the sodium bicarbonate crystals formed are carried in the liquor to the lter with little or no opportunity for sedimentation in the chambers.u Subjecting the owing liquor to the gradually increasing concentration of carbon dioxide gives control of the size of the sodium bicarbonate crystals formed. In comparison with standard practice the coarser crystals thus formed are filtered more readily and permit longer life of the lters because of the small proportion of iine crystals. They wash more readily with less water, hence less dilution of the filtrate and less liquor from which to recover ammonia. The crystals carry less adhering water to be removed in the calciner and returned to the circuit with the gases.
--The rate of feed automatically controls the liquor-level in each chamber by maintaining a static head pressure suicient to cause the'floW of the liquor.
When rate of operation, i. e., rate of brine feed, is established, the rate of absorption of CO2 is constant, and the size 0f the crystals remains uniform as long as that rate of feed is maintained. The constant operation, under the defined conditions, keeps the crystals in .continuous suspension, without sedimentation, thus permitting uninterrupted operation. In the usual cornmercial method each bicarbonate precipitation unit operates eiiiciently only 60% of the time because of the necessity of periodically removing sediment.
The unit may be operated eiciently at 10 to 100% of its capacity, thus permitting great flexibilty in production. The usual commercial unit can be operated only at about 70 to 100% of its 4 capacity. Operating costs are not moreA than two-thirds of that of the conventional equipment.
Because of the desired low CO2 pressure applied to the initial vessel of the series, it is highly desirable to apply additional CO2 to the other vessels to maintain the quantity of CO2 (still at 10W pressure) necessary for eflicient reaction. This is accomplished by means of the supplementary CO2 line I 4.
Gas unabsorbed in its passage through the chambers is conveyed to scrubbers for the recovery of ammonia and carbon dioxide carried by it.
The mechanical agitation prevents sedimentation regardless of the particular rate of flow through the unit, thus the rate of flow may be adjusted for maximum efficiency of the conversion reaction to sodium bicarbonate and maintained there indenitely. This will x the rate of operation of the whole system and thereafter control of the brine feed to the scrubbers regulates the operation; this affords continuous operation at a uniform rate throughout the Whole plant and greatly increased efliciency over the method now used.
A cooling system of any desired type is preferably incorporated in the unit to remove the heat of reaction and to cool the liquor in the discharge end of the system to as low a temperature as possible, in order to facilitate maintenance of the temperature-pressure equilibrium at the optimum level indicated.
Since the system comprises a plurality of selfcontained units or chambers, the cutting out of one or more of the chambers in a system may readily be accomplished by providing the necessary gas and liquor by-pass pipe lines, Thus, repairing of individual units may be carried out without disturbing the operation of the remainder of the system, and the number of units in use may be varied to meet requirements.
This application is a continuation in part of my application Serial No. 540,785 filed June 17, 1944, now patent No. 2,471,013.
What is claimed is:
l. A method of producing sodium bicarbonate which comprises arranging a series of at least four bodies of ammoniated brine in horizontally disposed relation to each other in a series of reaction chambers, feeding ammoniated brine in to thelower portion of the rst of said series of reaction chambers, passing a gravity flow of brine from the bottom zone of each chamber except the last of the series into the bottom zone of the adjacent succeeding chamber of the series, withdrawing the brine from the lower zone of the last chamber of the series and discharging it at atmospheric pressure at a higher level below the tops of said chambers to maintain a constant level of brine in the chambers, and passing a stream of gas containing carbon dioxide successively through the bodies of brine in said series from the last to the first thereof to maintain a concentration of carbon dioxide in said bodies of gradually increasing degree from the first to the lastI thereof, said stream of gas being passed through the bodies by separately pumping the unabsorbed gas from each chamber excepting the first of the series at a gauge pressure of from about v3 to about 5 pounds through each preceding chamber of the series, said pressure being only sufficient to overcome the static head pressure of the brine in the respective chamber, to maintain substantially atmospheric gas pressure on the surface of the body of brine in each of the chambers.
5 6 2. Method as defined in claim 1 in which addi- Number Name Y Date tional gas containing carbon dioxide is introduced 1,104,897 Howard July 28, 1914 into the stream of gas flowing from each chamber 1,282,799 Frasch Oct. 29, 1918 excepting the first to each preceding chamber to 1,799,354 Chesny Apr. 7, 1931 compensate for the carbon dioxide absorbed in 5 2,095,074 Muus Oct.*5, 1937 said chambers. 2,139,589 Ittner Dec. 6, 1938 JOHN ROSS TAYLOR. 2,191,467 Haywood Feb. 27, 1940 REFERENCES CITED OTHER REFERENCES Lunge Sulfuric Acid and Alkali V01. 3 Gurney The following references are of record in the 10 me of this patent: and Jackson, London, 1911, edition, pp. 92-102.
UNITED STATES PATENTS Number Name Date 308,083 Maguin Nov 18, 1884 15 940,595 Herreshoff Nov. 16, 1909

Claims (1)

1. A METHOD OF PRODUCING SODIUM BICARBONATE WHICH COMPRISES ARRANGING A SERIES OF AT LEAST FOUR BODIES OF AMMONIATED BRINE IN HORIZONTALLY DISPOSED RELATION TO EACH OTHER IN A SERIES OF REACTION CHAMBERS FEEDING AMMONIATED BRINE IN TO THE LOWER PORTION OF THE FIRST OF SAID SERIES OF REACTION CHAMBERS, PASSING A GRAVITY FLOW OF BRINE FROM THE BOTTOM ZONE OF EACH CHAMBER EXCEPT THE LAST OF THE SERIES INTO THE BOTTOM ZONE OF THE ADJACENT SUCCEDING CHAMBER OF THE SERIES, WITHDRAWING THE BRINE FROM THE LOWER ZONE OF THE LAST CHAMBER OF THE SERIES AND DISCHARGE IT AT ATMOSPHERIC PRESSURE AT A HIGHER LEVEL BELOW THE TOPS OF SAID CHAMBERS TO MAINTAIN A CONSTANT LEVEL OF BRINE IN THE CHAMBERS, AND PASSING A STREAM OF GAS CONTAINING CARBON DIOXIDE SUCCESSVIELY THROUGH THE BODIES OF BRINE IN SAID SERIES FROM THE LAST TO THE FIRST THEREOF TO MAINTAIN A CONCENTRATION OF CARBON DIOXIDE IN SAID BODIES OF GRADUALLY INCREASING DEGREE FROM THE FIRST TO THE LAST THEREOF, SAID STREAM OF GAS BEING PASSED THROUGH THE BODIES BY SEPARATELY PUMPING THE UNABSORBED GAS FROM EACH CHAMBER EXCEPTING THE FIRST OF THE SERIES AT A GAUGE PRESSURE OF FROM ABOUT 3 TO ABOUT 5 POUNDS THROUGH EACH PRECEDING CHAMBER OF THE SERIES, SAID PRESSURE BEING ONLY SUFFICIENT TO OVERCOME THE STATIC HEAD PRESSURE OF THE BRINE IN THE RESPECTIVE CHAMBER, TO MAINTAIN SUBSTANTIALLY ATMOSPHERIC GAS PRESSURE ON THE SURFACE OF THE BODY OF BRINE IN EACH OF THE CHAMBERS.
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2737440A (en) * 1951-09-11 1956-03-06 Chemical Construction Corp Manufacture of soda ash
US3120426A (en) * 1959-06-24 1964-02-04 Kaiser Aluminium Chem Corp Process for the production of aragonite crystals
US3198849A (en) * 1960-07-04 1965-08-03 Ballestra Mario Method and apparatus for effecting sulfonation
US3256068A (en) * 1961-10-03 1966-06-14 Burke Apparatus for the production of silica pigments
US3386810A (en) * 1961-10-03 1968-06-04 Burke Apparatus for the production of silica pigments
US3887693A (en) * 1972-05-26 1975-06-03 Derivados Del Fluor Sa Continuous process for obtaining aluminium fluoride by reacting fluosilicic acid with an aluminous material

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US308083A (en) * 1884-11-18 Apparatus for the manufacture of ammonia soda
US940595A (en) * 1906-02-10 1909-11-16 Gen Chemical Corp Purification of burner-gases.
US1104897A (en) * 1913-03-17 1914-07-28 Henry Howard Process of making bisulfite of soda.
US1282799A (en) * 1917-03-01 1918-10-29 Hans A Frasch Method of and apparatus for conveying and absorbing gases.
US1799354A (en) * 1929-01-21 1931-04-07 Heinz H Chesny Carbonating apparatus
US2095074A (en) * 1933-09-12 1937-10-05 Norsk Hydro Elek Sk Kvaeistofa Process for the production of sulphate of ammonium
US2139589A (en) * 1936-06-06 1938-12-06 Colgate Palmolive Peet Co Hydrolysis of fats and oils
US2191467A (en) * 1934-12-08 1940-02-27 West Virginia Pupl & Paper Com Apparatus for producing calcium sulphite

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US308083A (en) * 1884-11-18 Apparatus for the manufacture of ammonia soda
US940595A (en) * 1906-02-10 1909-11-16 Gen Chemical Corp Purification of burner-gases.
US1104897A (en) * 1913-03-17 1914-07-28 Henry Howard Process of making bisulfite of soda.
US1282799A (en) * 1917-03-01 1918-10-29 Hans A Frasch Method of and apparatus for conveying and absorbing gases.
US1799354A (en) * 1929-01-21 1931-04-07 Heinz H Chesny Carbonating apparatus
US2095074A (en) * 1933-09-12 1937-10-05 Norsk Hydro Elek Sk Kvaeistofa Process for the production of sulphate of ammonium
US2191467A (en) * 1934-12-08 1940-02-27 West Virginia Pupl & Paper Com Apparatus for producing calcium sulphite
US2139589A (en) * 1936-06-06 1938-12-06 Colgate Palmolive Peet Co Hydrolysis of fats and oils

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2737440A (en) * 1951-09-11 1956-03-06 Chemical Construction Corp Manufacture of soda ash
US3120426A (en) * 1959-06-24 1964-02-04 Kaiser Aluminium Chem Corp Process for the production of aragonite crystals
US3198849A (en) * 1960-07-04 1965-08-03 Ballestra Mario Method and apparatus for effecting sulfonation
US3256068A (en) * 1961-10-03 1966-06-14 Burke Apparatus for the production of silica pigments
US3386810A (en) * 1961-10-03 1968-06-04 Burke Apparatus for the production of silica pigments
US3887693A (en) * 1972-05-26 1975-06-03 Derivados Del Fluor Sa Continuous process for obtaining aluminium fluoride by reacting fluosilicic acid with an aluminous material

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