CA1038278A - Recovery of ammonia from underground storage - Google Patents
Recovery of ammonia from underground storageInfo
- Publication number
- CA1038278A CA1038278A CA263,008A CA263008A CA1038278A CA 1038278 A CA1038278 A CA 1038278A CA 263008 A CA263008 A CA 263008A CA 1038278 A CA1038278 A CA 1038278A
- Authority
- CA
- Canada
- Prior art keywords
- ammonia
- cavern
- gaseous
- gaseous ammonia
- heated
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C1/00—Ammonia; Compounds thereof
- C01C1/02—Preparation, purification or separation of ammonia
- C01C1/10—Separation of ammonia from ammonia liquors, e.g. gas liquors
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C9/00—Methods or apparatus for discharging liquefied or solidified gases from vessels not under pressure
- F17C9/02—Methods or apparatus for discharging liquefied or solidified gases from vessels not under pressure with change of state, e.g. vaporisation
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2223/00—Handled fluid before transfer, i.e. state of fluid when stored in the vessel or before transfer from the vessel
- F17C2223/01—Handled fluid before transfer, i.e. state of fluid when stored in the vessel or before transfer from the vessel characterised by the phase
- F17C2223/0146—Two-phase
- F17C2223/0153—Liquefied gas, e.g. LPG, GPL
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2223/00—Handled fluid before transfer, i.e. state of fluid when stored in the vessel or before transfer from the vessel
- F17C2223/03—Handled fluid before transfer, i.e. state of fluid when stored in the vessel or before transfer from the vessel characterised by the pressure level
- F17C2223/033—Small pressure, e.g. for liquefied gas
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2223/00—Handled fluid before transfer, i.e. state of fluid when stored in the vessel or before transfer from the vessel
- F17C2223/04—Handled fluid before transfer, i.e. state of fluid when stored in the vessel or before transfer from the vessel characterised by other properties of handled fluid before transfer
- F17C2223/042—Localisation of the removal point
- F17C2223/046—Localisation of the removal point in the liquid
- F17C2223/047—Localisation of the removal point in the liquid with a dip tube
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2225/00—Handled fluid after transfer, i.e. state of fluid after transfer from the vessel
- F17C2225/01—Handled fluid after transfer, i.e. state of fluid after transfer from the vessel characterised by the phase
- F17C2225/0107—Single phase
- F17C2225/0123—Single phase gaseous, e.g. CNG, GNC
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/01—Propulsion of the fluid
- F17C2227/0107—Propulsion of the fluid by pressurising the ullage
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/01—Propulsion of the fluid
- F17C2227/0128—Propulsion of the fluid with pumps or compressors
- F17C2227/0135—Pumps
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/01—Propulsion of the fluid
- F17C2227/0128—Propulsion of the fluid with pumps or compressors
- F17C2227/0171—Arrangement
- F17C2227/0178—Arrangement in the vessel
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/03—Heat exchange with the fluid
- F17C2227/0302—Heat exchange with the fluid by heating
- F17C2227/0306—Heat exchange with the fluid by heating using the same fluid
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/03—Heat exchange with the fluid
- F17C2227/0302—Heat exchange with the fluid by heating
- F17C2227/0332—Heat exchange with the fluid by heating by burning a combustible
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/03—Heat exchange with the fluid
- F17C2227/0367—Localisation of heat exchange
- F17C2227/0388—Localisation of heat exchange separate
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2265/00—Effects achieved by gas storage or gas handling
- F17C2265/01—Purifying the fluid
- F17C2265/012—Purifying the fluid by filtering
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2265/00—Effects achieved by gas storage or gas handling
- F17C2265/05—Regasification
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2270/00—Applications
- F17C2270/01—Applications for fluid transport or storage
- F17C2270/0142—Applications for fluid transport or storage placed underground
- F17C2270/0144—Type of cavity
- F17C2270/0149—Type of cavity by digging cavities
- F17C2270/0152—Salt caverns
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2270/00—Applications
- F17C2270/01—Applications for fluid transport or storage
- F17C2270/0142—Applications for fluid transport or storage placed underground
- F17C2270/0157—Location of cavity
- F17C2270/016—Location of cavity onshore
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Treating Waste Gases (AREA)
Abstract
ABSTRACT
A process for recovering gaseous ammonia from liquefied ammonia stored in an underground cavern includes heating gaseous ammonia to a temperature below that at which decomposition occurs and feeding it into the liquefied ammonia in the cavern. The release of the heated gaseous ammonia in the liquefied ammonia causes conversion of some of the liquid into gaseous form, and gaseous ammonia so formed is withdrawn from the cavern.
A process for recovering gaseous ammonia from liquefied ammonia stored in an underground cavern includes heating gaseous ammonia to a temperature below that at which decomposition occurs and feeding it into the liquefied ammonia in the cavern. The release of the heated gaseous ammonia in the liquefied ammonia causes conversion of some of the liquid into gaseous form, and gaseous ammonia so formed is withdrawn from the cavern.
Description
1~)38278 This invention relates to the recovery of ammonia from underground storage caverns, for example caverns made in natural salt deposits.
Because of the seasonal demand for ammonia and ammonia products, for example in the fertilizer industry, manufacturing capacity during off-seasons exceeds the rate of consumption. It is economic to produce excess ammonia at these times and store this excess for use during times of peak demand. Although under-ground storage of ammonia is known, this method of storage has not generally gained favour over use of above ground storage tanks, some of which are large enough to hold 40,000 tons of ammonia. Although many precautions are taken to provide safe above ground storage of ammonia, such as storage in remote areas on stable ground, there is a hazard of accidental release of large quantities of ammonia to the atmosphere. Underground ;
storage reduces this hazard substantially. However, known pro-cesses for the recovery of ammonia from underground caverns have disadvantages in their need of elaborate heat exchange and gas purification means. Some of the problems arise because the underground caverns are made from natural salt deposits and the salt contaminates the ammonia, particularly when it is withdrawn from the cavern in liquid form.
In United States patent No. 2,732,334 ~Pollack), gaseous ammonia is withdrawn from the region above the surface of liquefied ammonia stored in an underground salt cavern. The withdrawn gaseous ammonia is compressed without liquefying, and is returned to the cavern where it is passed through a heat exchange conduit immersed in the liquefied ammonia. The gaseous ammonia condenses in the immersed conduit, giving up heat which evaporates some of the stored liquid. The condensed ammonia is then pumped by a submerged pump from the immersed con~duit ~"~
., 103~
to an above ground outlet product line. This process therefore requires the presence of a heat exchange conduit and a pump sub-merged in the liquefied ammonia in the cavern.
In one embodiment of the process described in United States patent No. 2,713,775 (Cottle), an inert liquid, which is denser than ammonia and has a higher boiling point, such as pentane, is added to a salt cavern containing liquefied ammonia to cover heat exchanger piping and a pump. Ammonia gas is removed ` from above the liquid ammonia, compressed and passed through the submerged piping. ~eat given up to the pentane by the ammonia -~ gas is, in turn, given up to the layer of liquid ammonia above -it, some of which is thereby evaporated. The ammonia gas in -the submerged piping condenses as it loses heat to the pentane and is pumped to the surface, where it is separated from any en-trained pentane liquid. In another embodiment, liquid ammonia is removed from the cavern and passed through an evaporator in which a pentane layer is used to separate dissolved salt. The complications involved by the use of an inert liquid such as pentane are readily apparent.
~ 20 In the process described in United States patent No.
;; 2,878,165 (Cottle),ammonia gas is pumped into a salt cavern to move salt-containing liquid ammonia into an above ground puri-~i fication system where salt is separated. United States patent No. 2,901,403 (Adams) provides a process in which an inert gas, ~ -such as off-gas from ammonia synthesis,is introduced into a salt cavern containing liquid ammonia and dissolved salt with sufficient force to lift the liquid into an above ground separa- :--tor,where the inert gas is separated and recycled. Ammonia is then distilled from the salt solution. Again, the complicated 3 nature of these processes is readily apparent.
-.,.
Because of the seasonal demand for ammonia and ammonia products, for example in the fertilizer industry, manufacturing capacity during off-seasons exceeds the rate of consumption. It is economic to produce excess ammonia at these times and store this excess for use during times of peak demand. Although under-ground storage of ammonia is known, this method of storage has not generally gained favour over use of above ground storage tanks, some of which are large enough to hold 40,000 tons of ammonia. Although many precautions are taken to provide safe above ground storage of ammonia, such as storage in remote areas on stable ground, there is a hazard of accidental release of large quantities of ammonia to the atmosphere. Underground ;
storage reduces this hazard substantially. However, known pro-cesses for the recovery of ammonia from underground caverns have disadvantages in their need of elaborate heat exchange and gas purification means. Some of the problems arise because the underground caverns are made from natural salt deposits and the salt contaminates the ammonia, particularly when it is withdrawn from the cavern in liquid form.
In United States patent No. 2,732,334 ~Pollack), gaseous ammonia is withdrawn from the region above the surface of liquefied ammonia stored in an underground salt cavern. The withdrawn gaseous ammonia is compressed without liquefying, and is returned to the cavern where it is passed through a heat exchange conduit immersed in the liquefied ammonia. The gaseous ammonia condenses in the immersed conduit, giving up heat which evaporates some of the stored liquid. The condensed ammonia is then pumped by a submerged pump from the immersed con~duit ~"~
., 103~
to an above ground outlet product line. This process therefore requires the presence of a heat exchange conduit and a pump sub-merged in the liquefied ammonia in the cavern.
In one embodiment of the process described in United States patent No. 2,713,775 (Cottle), an inert liquid, which is denser than ammonia and has a higher boiling point, such as pentane, is added to a salt cavern containing liquefied ammonia to cover heat exchanger piping and a pump. Ammonia gas is removed ` from above the liquid ammonia, compressed and passed through the submerged piping. ~eat given up to the pentane by the ammonia -~ gas is, in turn, given up to the layer of liquid ammonia above -it, some of which is thereby evaporated. The ammonia gas in -the submerged piping condenses as it loses heat to the pentane and is pumped to the surface, where it is separated from any en-trained pentane liquid. In another embodiment, liquid ammonia is removed from the cavern and passed through an evaporator in which a pentane layer is used to separate dissolved salt. The complications involved by the use of an inert liquid such as pentane are readily apparent.
~ 20 In the process described in United States patent No.
;; 2,878,165 (Cottle),ammonia gas is pumped into a salt cavern to move salt-containing liquid ammonia into an above ground puri-~i fication system where salt is separated. United States patent No. 2,901,403 (Adams) provides a process in which an inert gas, ~ -such as off-gas from ammonia synthesis,is introduced into a salt cavern containing liquid ammonia and dissolved salt with sufficient force to lift the liquid into an above ground separa- :--tor,where the inert gas is separated and recycled. Ammonia is then distilled from the salt solution. Again, the complicated 3 nature of these processes is readily apparent.
-.,.
- 2 -,.
r , , . .
, ~'t ` ` 1038Z78 - It is therefore an object of the invention to provide a process for recovering ammonia from an underground cavern, such as a salt cavern, in a relatively uncontaminated state and with a less comp]icated withdrawal system than those pre-viously known.
~; According to the present invention, gaseous ammonia is heated to a temperature below that at which decomposition t~- occurs. The heated gaseous ammonia is then fed into the lique-fied ammonia in the cavern and released in the liquefied ammonia to cause conversion of some of the liquid ammonia into gaseous form. Ammonia gas thus formed is then withdrawn from the cavern.
:. ;, Such a process avoids the complications of the prior art and, ~0~ at the same time, enables ammonia gas of reasonable purity to -~ be recovered from a cavern such as a salt cavern.
, :~
The ammonia gas may be heated in any convenient manner, for example by a simple gas-fired heater or by passage through a heat exchanger provided with cycling heated fluid.
The heated gaseous ammonia is preferably sparged into the liquid ammonia near the centre of the cavern, away from the walls, and at sufficient depth to get good heat exchange by circulating : ~ ,t ~
~`~ the liquid ammonia.
.~
~ Ammonia gas withdrawn from the cavern is preferably : ..
passed through a mist eliminator which removes entrained liquid ~ droplets, such as droplets of ammonia-salt solution if a salt -. cavern is used. Better droplet removal is obtained if a low ` . .,,t, '`t gas velocity is maintained in the mist eliminator. Ammonia :- ..
~j~ gas containing less than 100 parts per million chloride may be . ,~.
*~ obtained in this way. A fine wire mesh, for example, stainless steel, mist eliminator may be used. Such gas purity is accept-able for direct application of the ammonia to soil as a fertilizer or in such chemical processes as the manufacture of urea. Some t~
: `,' .,~
: `~
;i.~
:, ' ' , lV38X~8 further purification may be necessary on the entry of the ammonia into a plant for the synthesis of nitric acid.
Advantageously, a portion of the ammonia gas with-drawn from the cavern is supplied to the heating step, and .~:
another portion of the ammonia gas withdrawn from the cavern is utilized elsewhere for whatever purpose it is required.
In the heating step, the gaseous ammonia is prefer--` ably heated to a temperature between about 260C. and about .
One embodiment of the present invention will now be -`
described, by way of example, with reference to the accompany-ing drawing, which shows a schematic view of an underground salt cavern in which ammonia is stored, together with means ; for recovering the ammonia therefrom.
`- Referring to the accompanying drawing, a sealed under-ground salt cavern 10 is filled by means of supply pipe 12 with liquid ammonia 14 to a depth preferably no~ exceeding 200 feet, ~ lea~ing a space 16 above the liquid ammonia for accumulation of `~ gaseous ammonia. Stored ammonia 14 is kept at about 116 psig . .~
~ pressure at a ground temperature of about 18C. Gaseous ammonia . .
is withdrawn through pipe 18, which passes through mist elimi-nator 20 for removal of entrained droplets of ammonia-salt solu-tion, accumulated liquid being withdrawn through drain 22. A
recycle portion passes to pump 24, while a product portion passes to pump 26. The product portion passes through pipe 28 to a cooler 30, where cooling water entering through inlet 32 lowers the temperature from about 65C. to about 38C., and thence ~`
~-~ passes through line 34 to a consuming operation.
` The recycle portion passes through pipe 36 at about 212 psig pressure to heat exchanger 38, in which cycling, tempera-ture-controlled fluid entering through inlet 40 heats the gaseous ammonia to a temperature below that at which decomposition occurs.
:
' : :
lQ38Z78 ~eated gaseous ammonia is then returned through pipe 42 to the ~; storage cavern where it is released in the liquid ammonia 14 from a sparger 44. The sparger 44 is preferably located near the centre of the cavern, away from its side walls, to minimize side wall erosion as the gaseous ammonia is mixed with th~ fluid ammonia, the sparger 44 being immersed at a depth that permits circulation of enough of the liquid to ensure good heat exchange.
The gaseous ammonia thus produced rises to space 16 for with-drawal through pipe 18.
Depending on the temperature of the heated gaseous ammonia entering the cavern through pipe 42, about 30 to 45 per ~` cent of the evaporated ammonia can be recovered as product. In ~ one specific example, with gas heated to 427C., 234,000 pounds per hour of gaseous ammonia were divided into a recovery stream of 100,000 pounds per hour or 43 per cent of the evaporated ammonia, and a recycle stream of 134,000 pounds per hour or 57 per cent of the evaporated ammonia. In another specific ~; example, with heating to 296C., 300,000 pounds per hour of .:~
gaseous ammonia were divided into recovery and recycle streams of 100,000 and 200,000 pounds per hour or 33 per cent and 67 per cent, respectively. A simple mist eliminator in which drop-- lets were retained on wire gauze decreased entrainment of -; chloride in the gaseous ammonia to less than 100 parts per million.
The described embodiment and specific examples ade-quately illustrate the simplicity and efficiency of the inven- -~ tion. Various other embodiments within the scope of the inven-qj tion will be apparent to the man skilled in the art, the scope of the invention being defined in the appended claims.
i 30 .
,' ,, , '~ :''. . .
r , , . .
, ~'t ` ` 1038Z78 - It is therefore an object of the invention to provide a process for recovering ammonia from an underground cavern, such as a salt cavern, in a relatively uncontaminated state and with a less comp]icated withdrawal system than those pre-viously known.
~; According to the present invention, gaseous ammonia is heated to a temperature below that at which decomposition t~- occurs. The heated gaseous ammonia is then fed into the lique-fied ammonia in the cavern and released in the liquefied ammonia to cause conversion of some of the liquid ammonia into gaseous form. Ammonia gas thus formed is then withdrawn from the cavern.
:. ;, Such a process avoids the complications of the prior art and, ~0~ at the same time, enables ammonia gas of reasonable purity to -~ be recovered from a cavern such as a salt cavern.
, :~
The ammonia gas may be heated in any convenient manner, for example by a simple gas-fired heater or by passage through a heat exchanger provided with cycling heated fluid.
The heated gaseous ammonia is preferably sparged into the liquid ammonia near the centre of the cavern, away from the walls, and at sufficient depth to get good heat exchange by circulating : ~ ,t ~
~`~ the liquid ammonia.
.~
~ Ammonia gas withdrawn from the cavern is preferably : ..
passed through a mist eliminator which removes entrained liquid ~ droplets, such as droplets of ammonia-salt solution if a salt -. cavern is used. Better droplet removal is obtained if a low ` . .,,t, '`t gas velocity is maintained in the mist eliminator. Ammonia :- ..
~j~ gas containing less than 100 parts per million chloride may be . ,~.
*~ obtained in this way. A fine wire mesh, for example, stainless steel, mist eliminator may be used. Such gas purity is accept-able for direct application of the ammonia to soil as a fertilizer or in such chemical processes as the manufacture of urea. Some t~
: `,' .,~
: `~
;i.~
:, ' ' , lV38X~8 further purification may be necessary on the entry of the ammonia into a plant for the synthesis of nitric acid.
Advantageously, a portion of the ammonia gas with-drawn from the cavern is supplied to the heating step, and .~:
another portion of the ammonia gas withdrawn from the cavern is utilized elsewhere for whatever purpose it is required.
In the heating step, the gaseous ammonia is prefer--` ably heated to a temperature between about 260C. and about .
One embodiment of the present invention will now be -`
described, by way of example, with reference to the accompany-ing drawing, which shows a schematic view of an underground salt cavern in which ammonia is stored, together with means ; for recovering the ammonia therefrom.
`- Referring to the accompanying drawing, a sealed under-ground salt cavern 10 is filled by means of supply pipe 12 with liquid ammonia 14 to a depth preferably no~ exceeding 200 feet, ~ lea~ing a space 16 above the liquid ammonia for accumulation of `~ gaseous ammonia. Stored ammonia 14 is kept at about 116 psig . .~
~ pressure at a ground temperature of about 18C. Gaseous ammonia . .
is withdrawn through pipe 18, which passes through mist elimi-nator 20 for removal of entrained droplets of ammonia-salt solu-tion, accumulated liquid being withdrawn through drain 22. A
recycle portion passes to pump 24, while a product portion passes to pump 26. The product portion passes through pipe 28 to a cooler 30, where cooling water entering through inlet 32 lowers the temperature from about 65C. to about 38C., and thence ~`
~-~ passes through line 34 to a consuming operation.
` The recycle portion passes through pipe 36 at about 212 psig pressure to heat exchanger 38, in which cycling, tempera-ture-controlled fluid entering through inlet 40 heats the gaseous ammonia to a temperature below that at which decomposition occurs.
:
' : :
lQ38Z78 ~eated gaseous ammonia is then returned through pipe 42 to the ~; storage cavern where it is released in the liquid ammonia 14 from a sparger 44. The sparger 44 is preferably located near the centre of the cavern, away from its side walls, to minimize side wall erosion as the gaseous ammonia is mixed with th~ fluid ammonia, the sparger 44 being immersed at a depth that permits circulation of enough of the liquid to ensure good heat exchange.
The gaseous ammonia thus produced rises to space 16 for with-drawal through pipe 18.
Depending on the temperature of the heated gaseous ammonia entering the cavern through pipe 42, about 30 to 45 per ~` cent of the evaporated ammonia can be recovered as product. In ~ one specific example, with gas heated to 427C., 234,000 pounds per hour of gaseous ammonia were divided into a recovery stream of 100,000 pounds per hour or 43 per cent of the evaporated ammonia, and a recycle stream of 134,000 pounds per hour or 57 per cent of the evaporated ammonia. In another specific ~; example, with heating to 296C., 300,000 pounds per hour of .:~
gaseous ammonia were divided into recovery and recycle streams of 100,000 and 200,000 pounds per hour or 33 per cent and 67 per cent, respectively. A simple mist eliminator in which drop-- lets were retained on wire gauze decreased entrainment of -; chloride in the gaseous ammonia to less than 100 parts per million.
The described embodiment and specific examples ade-quately illustrate the simplicity and efficiency of the inven- -~ tion. Various other embodiments within the scope of the inven-qj tion will be apparent to the man skilled in the art, the scope of the invention being defined in the appended claims.
i 30 .
,' ,, , '~ :''. . .
Claims (6)
1. A process for recovering gaseous ammonia from lique-fied ammonia stored in an underground cavern, comprising heating gaseous ammonia to a temperature below that at which decomposi-tion occurs, feeding said heated gaseous ammonia into the lique-fied ammonia in the cavern and releasing the heated gaseous ammonia in said liquefied ammonia to cause conversion of some of the liquid into gaseous form, and withdrawing gaseous ammonia from the cavern.
2. A process according to claim 1 wherein a portion of the ammonia gas withdrawn from the cavern is supplied to the heating step and another portion of the ammonia gas withdrawn from the cavern is utilized elsewhere.
3. A process according to claim 1 wherein the ammonia gas withdrawn from the cavern is passed through a mist eliminator to separate entrained liquid droplets therefrom.
4. A process according to claim 1 wherein the gaseous ammonia is heated to a temperature between about 260°C. and about 460°C.
5. A process for recovering gaseous ammonia from lique-fied ammonia stored in an underground salt cavern, comprising heating gaseous ammonia to a temperature below that at which decomposition occurs, feeding said heated gaseous ammonia into the liquefied ammonia in the cavern and releasing the heated gaseous ammonia in said liquefied ammonia to cause conversion of some of the liquefied ammonia into gaseous form, withdrawing gaseous ammonia through a mist eliminator to separate entrained liquid droplets containing dissolved salt therefrom, supplying a portion of said withdrawn ammonia gas to the heating step, and utilizing another portion of the withdrawn ammonia gas elsewhere.
6. A process according to claim 5 wherein the gaseous ammonia is heated to a temperature between about 260°C. and about 460°C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA263,008A CA1038278A (en) | 1976-10-08 | 1976-10-08 | Recovery of ammonia from underground storage |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA263,008A CA1038278A (en) | 1976-10-08 | 1976-10-08 | Recovery of ammonia from underground storage |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1038278A true CA1038278A (en) | 1978-09-12 |
Family
ID=4107023
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA263,008A Expired CA1038278A (en) | 1976-10-08 | 1976-10-08 | Recovery of ammonia from underground storage |
Country Status (1)
Country | Link |
---|---|
CA (1) | CA1038278A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2443640A1 (en) * | 1978-12-07 | 1980-07-04 | Equip Indls Et | Liquid gas evaporator construction - has mixer and super-heater to feed evaporator with hot gas |
-
1976
- 1976-10-08 CA CA263,008A patent/CA1038278A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2443640A1 (en) * | 1978-12-07 | 1980-07-04 | Equip Indls Et | Liquid gas evaporator construction - has mixer and super-heater to feed evaporator with hot gas |
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