CA1254365A - Sulphur trioxide absorption tower and process - Google Patents
Sulphur trioxide absorption tower and processInfo
- Publication number
- CA1254365A CA1254365A CA000496982A CA496982A CA1254365A CA 1254365 A CA1254365 A CA 1254365A CA 000496982 A CA000496982 A CA 000496982A CA 496982 A CA496982 A CA 496982A CA 1254365 A CA1254365 A CA 1254365A
- Authority
- CA
- Canada
- Prior art keywords
- sulphuric acid
- sulphur trioxide
- tower
- spray chamber
- stream
- 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
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 title claims abstract description 108
- 238000010521 absorption reaction Methods 0.000 title claims abstract description 70
- 238000000034 method Methods 0.000 title claims abstract description 20
- 230000008569 process Effects 0.000 title claims abstract description 20
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 60
- 235000011149 sulphuric acid Nutrition 0.000 claims abstract description 57
- 239000001117 sulphuric acid Substances 0.000 claims abstract description 57
- 239000007921 spray Substances 0.000 claims abstract description 55
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 239000005864 Sulphur Substances 0.000 claims description 6
- 238000005507 spraying Methods 0.000 claims description 6
- 230000000694 effects Effects 0.000 claims description 5
- 238000005260 corrosion Methods 0.000 abstract description 2
- 230000007797 corrosion Effects 0.000 abstract description 2
- 239000002253 acid Substances 0.000 description 66
- 238000012856 packing Methods 0.000 description 22
- 239000011449 brick Substances 0.000 description 9
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 8
- 230000008901 benefit Effects 0.000 description 7
- 230000003134 recirculating effect Effects 0.000 description 4
- 235000010269 sulphur dioxide Nutrition 0.000 description 4
- 239000004291 sulphur dioxide Substances 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 3
- 239000011473 acid brick Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 241000736911 Turritella communis Species 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B17/00—Sulfur; Compounds thereof
- C01B17/69—Sulfur trioxide; Sulfuric acid
- C01B17/74—Preparation
- C01B17/76—Preparation by contact processes
- C01B17/80—Apparatus
- C01B17/806—Absorbers; Heat exchangers
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B17/00—Sulfur; Compounds thereof
- C01B17/69—Sulfur trioxide; Sulfuric acid
- C01B17/74—Preparation
- C01B17/76—Preparation by contact processes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Gas Separation By Absorption (AREA)
- Treating Waste Gases (AREA)
Abstract
"Sulphur Trioxide Absorption Tower and Process"
An absorption tower for absorbing sulphur trioxide in sulphuric acid having a spray chamber wherein a major portion of sulphur trioxide is absorbed by a sulphuric acid spray and a packed absorption zone wherein remaining sulphur trioxide is absorbed into sulphuric acid. The spray chamber is optionally provided externally of the tower. Tower provides improved heat transfer and reduced corrosion within the tower.
An absorption tower for absorbing sulphur trioxide in sulphuric acid having a spray chamber wherein a major portion of sulphur trioxide is absorbed by a sulphuric acid spray and a packed absorption zone wherein remaining sulphur trioxide is absorbed into sulphuric acid. The spray chamber is optionally provided externally of the tower. Tower provides improved heat transfer and reduced corrosion within the tower.
Description
~254365 This invention relates to processes and apparatus for the generation of enriched sulphuric acid by the absorption of sulphur trioxide in sulphuric acid.
In the manufacture of sulphuric acid from sulphur dioxide in the classical contact process, a dry sulphur dioxide gas is obtained which is passed through a series of catalyst beds in which essentially all of the sulphur dioxide is converted to sulphur trioxide. The sulphur trioxide is then absorbed into sulphuric acid in one or more absorption towers to provide an enriched sulphuric acid stream.
Typically, the sulphur trioxide gas stream from the catalytic converter beds contains 5 - 13% by volume of sulphur trioxide and is generally cooled to a temperature in the order of 160 - 260C prior to the absorption stage. The sulphur trioxide is typically removed from the gaseous stream by countercurrent absorption with sulphuric acid within a brick lined packed absorption tower.
In consequence of the very large quantities of heat generated by the absorption of the sulphur trioxide and of the desire to avoid the throughput of unabsorbed sulphur trioxide in the effluent gas stream, absorption towers require a large acid throughput flow if overly hot, corrosive acid is to be avoided. Further, it is also desirable that broad acid concentration ranges be avoided through the use of sufficiently large absorber acid flow. Typically, an acid product removal stream may represent only 5 - 10~ of the circulating acid stream contained within the absorption ~:254365
In the manufacture of sulphuric acid from sulphur dioxide in the classical contact process, a dry sulphur dioxide gas is obtained which is passed through a series of catalyst beds in which essentially all of the sulphur dioxide is converted to sulphur trioxide. The sulphur trioxide is then absorbed into sulphuric acid in one or more absorption towers to provide an enriched sulphuric acid stream.
Typically, the sulphur trioxide gas stream from the catalytic converter beds contains 5 - 13% by volume of sulphur trioxide and is generally cooled to a temperature in the order of 160 - 260C prior to the absorption stage. The sulphur trioxide is typically removed from the gaseous stream by countercurrent absorption with sulphuric acid within a brick lined packed absorption tower.
In consequence of the very large quantities of heat generated by the absorption of the sulphur trioxide and of the desire to avoid the throughput of unabsorbed sulphur trioxide in the effluent gas stream, absorption towers require a large acid throughput flow if overly hot, corrosive acid is to be avoided. Further, it is also desirable that broad acid concentration ranges be avoided through the use of sufficiently large absorber acid flow. Typically, an acid product removal stream may represent only 5 - 10~ of the circulating acid stream contained within the absorption ~:254365
- 2 - C-I-L 695 tower packing and ancillary piping. Using materials which are economically available, acid temperatures typically range up to 120C.
Countercurrent downward acid flow and upwards gas flow through the tower packing requires the tower to be designed to provide sufficient empty space to allow the two fluids to interact and pass each other and to avoid the situation known as "flooding" wherein the gas flow prevents liquid drainage through the packing. This problem ln is most serious where the gas first enters the packing because this is where the gas flow is largest due to the sulphur trioxide present in the gas and the hottest (thus, lowest density) and results in the largest volume of gas to flow through the void spaces in the packing. Compounding the problem is that the downward liquid flow is also largest in the lower packing region as a result of the acid absorbing most of the sulphur trioxide from the gas in this region.
Absorption towers of present design require distributors at the top of the packing in order to spread the incoming absorbing acid over the packing so that all of the surfaces of the packing is wetted to effect maximum absorption of the sulphur trioxide.
A serious disadvantage of conventional absorption towers is the need for thick brick linings within the tower in order to avoid the presence of hot tower shells and hot linings behind the brick. Hot gas (160 - 260C) is fed, typically, into the lower region of the tower immediately adjacent the brick lining - which is, disadvantageously, only intermittently wetted. Such brick linings add to the cost of a tower and are difficult to install properly.
In addition, there are, typically, two conflicting needs which must be satisfied in the removal of sulphur trioxide by acid absorption. There is a need for the gross removal of sulphur trioxide from the gas without exceeding ~Z5436S
Countercurrent downward acid flow and upwards gas flow through the tower packing requires the tower to be designed to provide sufficient empty space to allow the two fluids to interact and pass each other and to avoid the situation known as "flooding" wherein the gas flow prevents liquid drainage through the packing. This problem ln is most serious where the gas first enters the packing because this is where the gas flow is largest due to the sulphur trioxide present in the gas and the hottest (thus, lowest density) and results in the largest volume of gas to flow through the void spaces in the packing. Compounding the problem is that the downward liquid flow is also largest in the lower packing region as a result of the acid absorbing most of the sulphur trioxide from the gas in this region.
Absorption towers of present design require distributors at the top of the packing in order to spread the incoming absorbing acid over the packing so that all of the surfaces of the packing is wetted to effect maximum absorption of the sulphur trioxide.
A serious disadvantage of conventional absorption towers is the need for thick brick linings within the tower in order to avoid the presence of hot tower shells and hot linings behind the brick. Hot gas (160 - 260C) is fed, typically, into the lower region of the tower immediately adjacent the brick lining - which is, disadvantageously, only intermittently wetted. Such brick linings add to the cost of a tower and are difficult to install properly.
In addition, there are, typically, two conflicting needs which must be satisfied in the removal of sulphur trioxide by acid absorption. There is a need for the gross removal of sulphur trioxide from the gas without exceeding ~Z5436S
- 3 - C-I-L 695 the concentration and temperature limits set on the sulphuric acid used, and a second need for removing substantially all of the sulphur trioxide in the gas to efficiency levels approaching 99.9% and higher.
The first need is normally achieved in the bottom lS - 20% of the packing in the tower, i.e. the first part of the packing which contacts the inlet gas. This need determines the tower diameter and is thus a fundamental factor in tower costs. The remaining 80 - 85% of the packing effects the sulphur trioxide absorption to the high levels required by environmental authorities and for which there is no need for such a large diameter tower or large acid flow.
Thus, there is a further disadvantage in conventional absorption towers in that the towers are oversized at the top in relation to the remaining part of the tower and the gas density and flow and acid flow in that upper part.
Modern processes for the manufacture of sulphuric acid using the double absorption system have two absorber towers, each of which suffer from the above disadvantages.
It is an object of the present invention to provide an absorption tower and process wherein the tower size and acid circulation rate in the tower packing region are reduced below conventional size.
It is a further object of the invention to reduce the detrimental effect of the gas on the materials of construction in the bottom of the tower so that thinner or no brick linings may be used.
Accordingly, in one of its aspects, the invention provides a sulphur trioxide absorption tower comprising:
(a) a shell;
(b) a sulphuric acid spray chamber within a lower part of said shell;
(c) a sulphur trioxide packed absorption zone above said spray chamber within said shell;
~25436S
The first need is normally achieved in the bottom lS - 20% of the packing in the tower, i.e. the first part of the packing which contacts the inlet gas. This need determines the tower diameter and is thus a fundamental factor in tower costs. The remaining 80 - 85% of the packing effects the sulphur trioxide absorption to the high levels required by environmental authorities and for which there is no need for such a large diameter tower or large acid flow.
Thus, there is a further disadvantage in conventional absorption towers in that the towers are oversized at the top in relation to the remaining part of the tower and the gas density and flow and acid flow in that upper part.
Modern processes for the manufacture of sulphuric acid using the double absorption system have two absorber towers, each of which suffer from the above disadvantages.
It is an object of the present invention to provide an absorption tower and process wherein the tower size and acid circulation rate in the tower packing region are reduced below conventional size.
It is a further object of the invention to reduce the detrimental effect of the gas on the materials of construction in the bottom of the tower so that thinner or no brick linings may be used.
Accordingly, in one of its aspects, the invention provides a sulphur trioxide absorption tower comprising:
(a) a shell;
(b) a sulphuric acid spray chamber within a lower part of said shell;
(c) a sulphur trioxide packed absorption zone above said spray chamber within said shell;
~25436S
- 4 - C-I-L 695 (d) means for spraying a sulphuric acid stream within said spray chamber;
(e) means for feeding a hot gas stream containing sulphur trioxide to said spray chamber,wherein a depleted sulphur trioxide gas stream is produced;
(f) means for feeding said depleted sulphur trioxide gas stream to said packed absorption zone;
(g) means for feeding a sulphuric acid stream to said packed absorption zone;
(h) means for collecting sulphuric acid stream from : said spray chamber and said absorption zone; and (i) means for collecting resultant gas stream from said packed absorption zone.
In a preferred feature the invention provides a tower as hereinbefore defined further comprising a side spray chamber external of said tower and connected to said sulphuric acid spray chamber.
In a further aspect, the invention provides a process for producing concentrated sulphuric acid from a hot gas stream containing sulphur trioxide, which process comprises:
: (a) feeding said gas stream to a sulphuric acid spray ; chamber contained within an absorption tower;
(b) spraying a first recycled sulphuric acid stream within said spray chamber to effect absorption of a major portion of said sulphur trioxide from said gas stream into said recycled sulphuric acid to produce a first enriched sulphuric acid stream and a depleted sulphur trioxide gas stream;
(c) feeding said depleted sulphur trioxide gas stream to a sulphur trioxide packed absorption zone above said spray chamber within said absorption tower;
(d) feeding a second recycled sulphuric acid stream to said sulphur trioxide absorption zone to e~fect absorption of substantially all of said sulphur trioxide remaining in said depleted sulphur trioxide ~25436S
(e) means for feeding a hot gas stream containing sulphur trioxide to said spray chamber,wherein a depleted sulphur trioxide gas stream is produced;
(f) means for feeding said depleted sulphur trioxide gas stream to said packed absorption zone;
(g) means for feeding a sulphuric acid stream to said packed absorption zone;
(h) means for collecting sulphuric acid stream from : said spray chamber and said absorption zone; and (i) means for collecting resultant gas stream from said packed absorption zone.
In a preferred feature the invention provides a tower as hereinbefore defined further comprising a side spray chamber external of said tower and connected to said sulphuric acid spray chamber.
In a further aspect, the invention provides a process for producing concentrated sulphuric acid from a hot gas stream containing sulphur trioxide, which process comprises:
: (a) feeding said gas stream to a sulphuric acid spray ; chamber contained within an absorption tower;
(b) spraying a first recycled sulphuric acid stream within said spray chamber to effect absorption of a major portion of said sulphur trioxide from said gas stream into said recycled sulphuric acid to produce a first enriched sulphuric acid stream and a depleted sulphur trioxide gas stream;
(c) feeding said depleted sulphur trioxide gas stream to a sulphur trioxide packed absorption zone above said spray chamber within said absorption tower;
(d) feeding a second recycled sulphuric acid stream to said sulphur trioxide absorption zone to e~fect absorption of substantially all of said sulphur trioxide remaining in said depleted sulphur trioxide ~25436S
- 5 - C-I-L 695 gas stream to produce a second enriched sulphuric acid stream and a substantially sulphur trioxide-free gas stream;
(e) collecting said first and second enriched sulphuric acid streams; and (f) collecting said substantially sulphur trioxide-free gas stream.
The first and second recycled acid streams fed to the spray chamber and the packed absorption zone, respectively, may come from a direct common source, or each may emanate from a suitable and distinct acid circuit found within a full sulphuric acid manufacturing plant. For example, the recycled acid to the packed absorption tower may be fed also from either a drying, primary or final tower acid circuit or any combination thereof. The acid fed to the spray chamber may emanate from any of the above packed absorption zone acid sources or yet a further separate circuit. Preferably, the two feed acids emanate from a common source of circulating acid with the volume of spray chamber acid being greater than the volume of packed absorption zone acid.
Thus, in a preferred feature the invention provides a process as hereinbefore defined wherein said first recycled sulphuric acid stream constitutes a major portion of a recycled common sulphuric acid stream and said second recycled sulphuric acid stream constitutes a minor portion of said recycled common sulphuric acid stream.
The relative amounts of recycled acid fed to the packed absorption zone and spray chamber is determined by the acid temperatures and concentrations of the enriched acid streams desired. Under normal operating conditions, the acid flow requirement to the spray chamber will normally exceed that to the packed absorption zone.
However, in the case where energy recovery or other considerations are of concern, it is possible that the ~25436~i
(e) collecting said first and second enriched sulphuric acid streams; and (f) collecting said substantially sulphur trioxide-free gas stream.
The first and second recycled acid streams fed to the spray chamber and the packed absorption zone, respectively, may come from a direct common source, or each may emanate from a suitable and distinct acid circuit found within a full sulphuric acid manufacturing plant. For example, the recycled acid to the packed absorption tower may be fed also from either a drying, primary or final tower acid circuit or any combination thereof. The acid fed to the spray chamber may emanate from any of the above packed absorption zone acid sources or yet a further separate circuit. Preferably, the two feed acids emanate from a common source of circulating acid with the volume of spray chamber acid being greater than the volume of packed absorption zone acid.
Thus, in a preferred feature the invention provides a process as hereinbefore defined wherein said first recycled sulphuric acid stream constitutes a major portion of a recycled common sulphuric acid stream and said second recycled sulphuric acid stream constitutes a minor portion of said recycled common sulphuric acid stream.
The relative amounts of recycled acid fed to the packed absorption zone and spray chamber is determined by the acid temperatures and concentrations of the enriched acid streams desired. Under normal operating conditions, the acid flow requirement to the spray chamber will normally exceed that to the packed absorption zone.
However, in the case where energy recovery or other considerations are of concern, it is possible that the ~25436~i
- 6 - C-I-L 695 relative flow relationship may vary such that the reverse is true. One such case wouId be when very hot acid from the spray chamber is desired which would call for a reduced volume of feed recycled acid to the spray chamber.
The two enriched acid streams may either be combined within the tower to exit as an admixture of acids, or be run off the tower as distinct streams emanating from the packed absorption zone and spray chamber, separately. In the former case, in which the two enriched acid streams are combined, it is deemed that this results in a "common"
'' circuit of acid transfer insofar as it relates to the process according to the invention. On the other hand, by the term "separate" circuit is meant that there is no direct mixing of the enriched acid streams exiting from the packed absorption zone and spray chamber.
Thus, it can be seen that the enriched acids produced in the two distinct regions of the tower may be optionally combined either together and/or with any other appropriate acid circulating within a full sulphuric acid plant.
In a preferred feature the enriched acid from the packed absorption zone is allowed to pass through the spray chamber and thus becomes combined with the enriched acid from the spray chamber.
In order that the invention may be better understood, preferred embodiments according to the invention will now be described, by way of example only, with reference to the accompanying drawings wherein:
Figure 1 shows a vertical sectional view of a sulphur trioxide absorption tower according to the invention;
Figure 2 shows a schematic sectional view of an array of acid sprayers disposed within the tower of Figure l;
Figure 3 shows a vertical sectional view of the tower ~i of Figure 1 provided with a side array of acid sprayers, and
The two enriched acid streams may either be combined within the tower to exit as an admixture of acids, or be run off the tower as distinct streams emanating from the packed absorption zone and spray chamber, separately. In the former case, in which the two enriched acid streams are combined, it is deemed that this results in a "common"
'' circuit of acid transfer insofar as it relates to the process according to the invention. On the other hand, by the term "separate" circuit is meant that there is no direct mixing of the enriched acid streams exiting from the packed absorption zone and spray chamber.
Thus, it can be seen that the enriched acids produced in the two distinct regions of the tower may be optionally combined either together and/or with any other appropriate acid circulating within a full sulphuric acid plant.
In a preferred feature the enriched acid from the packed absorption zone is allowed to pass through the spray chamber and thus becomes combined with the enriched acid from the spray chamber.
In order that the invention may be better understood, preferred embodiments according to the invention will now be described, by way of example only, with reference to the accompanying drawings wherein:
Figure 1 shows a vertical sectional view of a sulphur trioxide absorption tower according to the invention;
Figure 2 shows a schematic sectional view of an array of acid sprayers disposed within the tower of Figure l;
Figure 3 shows a vertical sectional view of the tower ~i of Figure 1 provided with a side array of acid sprayers, and
- 7 - C-I-L 695 Figures 4, 5 and 6 show, schematically, acid circulation systems associated with an absorption tower according to the invention.
The absorption tower shown in Figure 1 comprises a carbon steel shell 11 having an effluent gas outlet 12 at the top and a hot gas inlet 13 and an acid outlet 14 at the bottom.
Shell 11 at its lower part has an inner lining 15 formed of acid resistant brick and a ceramic support 16, which together with the bottom of the shell define a sulphuric acid spray chamber 17. Disposed within chamber 17 is an array of acid distribution sprayers 18 leading from an acid inlet 19.
Within shell 11 above support 16 is a sulphur trioxide absorption zone 20 packed with ceramic saddle packing through which gas and acid may percolate to produce a full and intimate contact therebetween.
Shell 11 at an upper part has an acid inlet 21 and a cast iron acid distributor 22 above which is a mist eliminator 23 formed of glass fibre contained in a stainless steel frame.
Figure 2 shows the array of acid sprayers 18 constituted as a plurality of parallel pipes having a plurality of low pressure drop nozzles 24. An alternative array of sprayers may be arranged as a radial array of nozzles within the spray chamber.
The spray array constituting the means for spraying sulphuric acid within spray chamber 17 could, in alternative embodiments, produce acid as co-current, countercurrent or cross-flow streams as there is no back pressure of sulphur trioxide over the sulphuric acid. The array of sprayers would be, typically, inspectable and replaceable.
Figure 3 shows a more preferred absorption tower i according to the invention in which shell 11 of Figure 1 has been modified to have affixed thereto a hot gas
The absorption tower shown in Figure 1 comprises a carbon steel shell 11 having an effluent gas outlet 12 at the top and a hot gas inlet 13 and an acid outlet 14 at the bottom.
Shell 11 at its lower part has an inner lining 15 formed of acid resistant brick and a ceramic support 16, which together with the bottom of the shell define a sulphuric acid spray chamber 17. Disposed within chamber 17 is an array of acid distribution sprayers 18 leading from an acid inlet 19.
Within shell 11 above support 16 is a sulphur trioxide absorption zone 20 packed with ceramic saddle packing through which gas and acid may percolate to produce a full and intimate contact therebetween.
Shell 11 at an upper part has an acid inlet 21 and a cast iron acid distributor 22 above which is a mist eliminator 23 formed of glass fibre contained in a stainless steel frame.
Figure 2 shows the array of acid sprayers 18 constituted as a plurality of parallel pipes having a plurality of low pressure drop nozzles 24. An alternative array of sprayers may be arranged as a radial array of nozzles within the spray chamber.
The spray array constituting the means for spraying sulphuric acid within spray chamber 17 could, in alternative embodiments, produce acid as co-current, countercurrent or cross-flow streams as there is no back pressure of sulphur trioxide over the sulphuric acid. The array of sprayers would be, typically, inspectable and replaceable.
Figure 3 shows a more preferred absorption tower i according to the invention in which shell 11 of Figure 1 has been modified to have affixed thereto a hot gas
- 8 - C-I-L 695 conduit 25 formed of steel and lined with acid resistant brick 26. The sides of conduit 25 define a side spray chamber 27 external of the tower and within which chamber 26 is a side array of acid sprayers 28.
In an alternative form of the tower of Figure 3 the spray array may be disposed within an external enlarged downflowing vertical duct to treat the hot sulphur trioxide gas prior to entry to the tower.
Figure 4 shows a recycled common acid circuit associated with an absorption tower wherein the first and second enriched sulphuric acid streams from the spray chamber and packed absorption zone, respectively, are combined within the tower and run off to pump tank 29.
Acid from tank 29 is recirculated and cooled through heat exchanger 30 to spray chamber 17 and packed absorption zone 20 in major and minor amounts respectively. A product take-off line 31 is suitably located as shown.
Figure 5 shows an alternative recycled common acid circuit wherein the heat exchanger 30 is positioned after the spray chamber acid stream take-off point and prior to packed absorption zone entry. Such an arrangement permits higher temperatures to be optionally attained by the bulk of the total recirculating acid.
Figure 6 shows separate acid recirculation circuits for the packed absorption zone and spray chamber. A
separate feed and acid circuit for the spray chamber permits higher temperature enriched acid to be produced for higher energy recovery.
In operation, the towers according to the invention represent primary absorbers of use in a typical 2,000 STPD
sulphuric acid plant, which receive a sulphur trioxide gas stream at 200C obtained from the 93% conversion of a 12%
sulphur dioxide stream.
' With reference to Figures 1 and 4, a common recirculating acid flow of 4,000 USGPM overall enters the tower at 80C
and 98.5% strength. A major portion (2500 gpm) is fed to ~254365
In an alternative form of the tower of Figure 3 the spray array may be disposed within an external enlarged downflowing vertical duct to treat the hot sulphur trioxide gas prior to entry to the tower.
Figure 4 shows a recycled common acid circuit associated with an absorption tower wherein the first and second enriched sulphuric acid streams from the spray chamber and packed absorption zone, respectively, are combined within the tower and run off to pump tank 29.
Acid from tank 29 is recirculated and cooled through heat exchanger 30 to spray chamber 17 and packed absorption zone 20 in major and minor amounts respectively. A product take-off line 31 is suitably located as shown.
Figure 5 shows an alternative recycled common acid circuit wherein the heat exchanger 30 is positioned after the spray chamber acid stream take-off point and prior to packed absorption zone entry. Such an arrangement permits higher temperatures to be optionally attained by the bulk of the total recirculating acid.
Figure 6 shows separate acid recirculation circuits for the packed absorption zone and spray chamber. A
separate feed and acid circuit for the spray chamber permits higher temperature enriched acid to be produced for higher energy recovery.
In operation, the towers according to the invention represent primary absorbers of use in a typical 2,000 STPD
sulphuric acid plant, which receive a sulphur trioxide gas stream at 200C obtained from the 93% conversion of a 12%
sulphur dioxide stream.
' With reference to Figures 1 and 4, a common recirculating acid flow of 4,000 USGPM overall enters the tower at 80C
and 98.5% strength. A major portion (2500 gpm) is fed to ~254365
- 9 - C-I-L 69S
the spray chamber and a minor portion ~1500 gpm) to the packed absorption tower.
In the embodiments shown the diameter of the tower across the packed absorption zone measures 20 feet and requires only a 12 feet depth of typical 3" saddle packing.
This is to be contrasted wlth the need for a 20 feet depth of packing in a tower of conventional design to achieve the same performance of sulphur trioxide removal.
The acLd leaving the bottom of the tower through outlet 14 typically leaves at 120C and of 99.2% strength.
The sulphur trloxlde ab~orptlon efflclency is,typically, ln exce~s of 99.99%
In a modifled process, with reference to Figures 1 and 5 the recirculating sulphuric acld enterlng the tower through packed absorption zone inlet 21 is at a lower temperature than that entering through spray chamber inlet 19. The acid flow through inlet 19 may be cooled only to 100C whereais that through inlet 21 cooled to 80C. In this case, 84% of the total heat is now available for heat transfer above 100C in contrast to only 51~ of the total heat as seen in the first example process wherein both acid flows were cooled to 80C.
The advantage in heat removal by separation of the two dutles allows of significant deslgn flexibility not present in conventional single tower concepts.
! Thus, it can be seen that the improvement in sulphur trioxide absorptlon in sulphuric acid provided by the present lnventlon lles ln the use of sprays of absorbing acid to pre-absorb sulphur trioxlde from the gas stream prior to entering the packing mass, with such sprays being located typlcally in an unpacked space below the packing and optionally, in the inlet gas duct. The acid stream used for the sprays is the main portion of the recirculating acid in the absorbing system, with the minor portion being used to irrigate the absorption tower packing.
. . .
:, ., ,, ~," ~
':
., .
" ~254365
the spray chamber and a minor portion ~1500 gpm) to the packed absorption tower.
In the embodiments shown the diameter of the tower across the packed absorption zone measures 20 feet and requires only a 12 feet depth of typical 3" saddle packing.
This is to be contrasted wlth the need for a 20 feet depth of packing in a tower of conventional design to achieve the same performance of sulphur trioxide removal.
The acLd leaving the bottom of the tower through outlet 14 typically leaves at 120C and of 99.2% strength.
The sulphur trloxlde ab~orptlon efflclency is,typically, ln exce~s of 99.99%
In a modifled process, with reference to Figures 1 and 5 the recirculating sulphuric acld enterlng the tower through packed absorption zone inlet 21 is at a lower temperature than that entering through spray chamber inlet 19. The acid flow through inlet 19 may be cooled only to 100C whereais that through inlet 21 cooled to 80C. In this case, 84% of the total heat is now available for heat transfer above 100C in contrast to only 51~ of the total heat as seen in the first example process wherein both acid flows were cooled to 80C.
The advantage in heat removal by separation of the two dutles allows of significant deslgn flexibility not present in conventional single tower concepts.
! Thus, it can be seen that the improvement in sulphur trioxide absorptlon in sulphuric acid provided by the present lnventlon lles ln the use of sprays of absorbing acid to pre-absorb sulphur trioxlde from the gas stream prior to entering the packing mass, with such sprays being located typlcally in an unpacked space below the packing and optionally, in the inlet gas duct. The acid stream used for the sprays is the main portion of the recirculating acid in the absorbing system, with the minor portion being used to irrigate the absorption tower packing.
. . .
:, ., ,, ~," ~
':
., .
" ~254365
- 10 - C-I-L 695 Many advantages stem from the pre-absorption process described hereinabove.
First, the brick or metal in the initial gas zone in which sprays are used is continually irrigated with cool acid, which protect the linings behind the brick. Also, thinner brick linings can be used, which result in savings in caPital cost.
In alternative embodiments, the use of recently developed corrosion resistant metals in the initial gas zone of the tower in the practise of the invention allows for the complete elimination of acid brick.
A second advantage lies in the use of a tower of smaller size as a result of the reduced gas flow, higher gas density, and reduced liquid flow required over the packing.
Typically,tower diameter can be reduced up to 25% for the process according to the invention.
A third advantage lies in the reduction in acid flow in the distribution system, which allows of the use of smaller pipe, and the like to the tower top.
Yet a further advantage lies in the ability to vary the acid flow to the sprays in response to changes in sulphur trioxide absorption while leaving the irrigation over the packing unchanged. Conventional distributors are not readily turned down in flow whereas spray systems can be 25 designed which can operate at reduced pressure or with individual nozzles shut off if needed. This advantage is particularly useful if energy recovery is to be practiced in the absorption process.
A still further advantage lies in the separation of 30 the main heat removal operation associated with the sprays, where a low acid temperature is not essential, from the cooling in the packing where good cooling is required.
First, the brick or metal in the initial gas zone in which sprays are used is continually irrigated with cool acid, which protect the linings behind the brick. Also, thinner brick linings can be used, which result in savings in caPital cost.
In alternative embodiments, the use of recently developed corrosion resistant metals in the initial gas zone of the tower in the practise of the invention allows for the complete elimination of acid brick.
A second advantage lies in the use of a tower of smaller size as a result of the reduced gas flow, higher gas density, and reduced liquid flow required over the packing.
Typically,tower diameter can be reduced up to 25% for the process according to the invention.
A third advantage lies in the reduction in acid flow in the distribution system, which allows of the use of smaller pipe, and the like to the tower top.
Yet a further advantage lies in the ability to vary the acid flow to the sprays in response to changes in sulphur trioxide absorption while leaving the irrigation over the packing unchanged. Conventional distributors are not readily turned down in flow whereas spray systems can be 25 designed which can operate at reduced pressure or with individual nozzles shut off if needed. This advantage is particularly useful if energy recovery is to be practiced in the absorption process.
A still further advantage lies in the separation of 30 the main heat removal operation associated with the sprays, where a low acid temperature is not essential, from the cooling in the packing where good cooling is required.
Claims (6)
1. A process for producing concentrated sulphuric acid from a hot gas stream containing sulphur trioxide, which process comprises:
(a) feeding said gas stream to an unpacked sulphuric acid spray chamber contained within an absorption tower;
(b) spraying a first recycled sulphuric acid stream within said spray chamber to effect absorption of a major portion of said sulphur trioxide from said gas stream into said recycled sulphuric acid to produce a first enriched sulphuric acid stream and a depleted sulphur trioxide gas stream;
(c) feeding said depleted sulphur trioxide gas stream to a sulphur trioxide packed absorption zone above said spray chamber within said absorption tower;
(d) feeding a second recycled sulphuric acid stream to said sulphur trioxide absorption zone to effect absorption of substantially all of said sulphur trioxide remaining in said depleted sulphur trioxide gas stream to produce a second enriched sulphuric acid stream and a substantially sulphur trioxide-free gas stream;
(e) collecting said first and second enriched sulphuric acid streams; and (f) collecting said substantially sulphur trioxide-free gas stream.
(a) feeding said gas stream to an unpacked sulphuric acid spray chamber contained within an absorption tower;
(b) spraying a first recycled sulphuric acid stream within said spray chamber to effect absorption of a major portion of said sulphur trioxide from said gas stream into said recycled sulphuric acid to produce a first enriched sulphuric acid stream and a depleted sulphur trioxide gas stream;
(c) feeding said depleted sulphur trioxide gas stream to a sulphur trioxide packed absorption zone above said spray chamber within said absorption tower;
(d) feeding a second recycled sulphuric acid stream to said sulphur trioxide absorption zone to effect absorption of substantially all of said sulphur trioxide remaining in said depleted sulphur trioxide gas stream to produce a second enriched sulphuric acid stream and a substantially sulphur trioxide-free gas stream;
(e) collecting said first and second enriched sulphuric acid streams; and (f) collecting said substantially sulphur trioxide-free gas stream.
2. A process as claimed in Claim 1 wherein said first recycled sulphuric acid stream constitutes a major portion of a recycled common sulphuric acid stream and said second recycled sulphuric acid stream constitutes a minor portion of said recycled common sulphuric acid stream.
3. A process as claimed in Claim 1 wherein said first and second enriched sulphuric acid streams are combined.
4. A process as claimed in any one of Claims 1, 2 or 3 further comprising spraying said gas stream with a part of said first recycled sulphuric acid within a side spray chamber external of said tower and connected to said sulphuric acid chamber, prior to feeding said gas stream to said sulphuric acid chamber.
5. A sulphur trioxide absorption tower comprising (a) a shell;
(b) a sulphuric acid spray chamber within a lower part of said shell;
(c) a sulphur trioxide packed absorption zone above said spray chamber within said shell;
(d) means for spraying a sulphuric acid stream within said spray chamber;
(e) means for feeding a hot gas stream containing sulphur trioxide to said spray chamber wherein a depleted sulphur trioxide gas stream is produced;
(f) means for feeding said depleted sulphur trioxide gas stream to said packed absorption zone;
(g) means for feeding a sulphuric acid stream to said packed absorption zone;
(h) means for collecting sulphuric acid stream from said spray chamber and said absorption zone; and (i) means for collecting resultant gas stream from said packed absorption zone.
(b) a sulphuric acid spray chamber within a lower part of said shell;
(c) a sulphur trioxide packed absorption zone above said spray chamber within said shell;
(d) means for spraying a sulphuric acid stream within said spray chamber;
(e) means for feeding a hot gas stream containing sulphur trioxide to said spray chamber wherein a depleted sulphur trioxide gas stream is produced;
(f) means for feeding said depleted sulphur trioxide gas stream to said packed absorption zone;
(g) means for feeding a sulphuric acid stream to said packed absorption zone;
(h) means for collecting sulphuric acid stream from said spray chamber and said absorption zone; and (i) means for collecting resultant gas stream from said packed absorption zone.
6. A tower as claimed in Claim 5 further comprising a side spray chamber external of said tower and connected to said sulphuric acid spray chamber.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000496982A CA1254365A (en) | 1985-12-05 | 1985-12-05 | Sulphur trioxide absorption tower and process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000496982A CA1254365A (en) | 1985-12-05 | 1985-12-05 | Sulphur trioxide absorption tower and process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1254365A true CA1254365A (en) | 1989-05-23 |
Family
ID=4132021
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000496982A Expired CA1254365A (en) | 1985-12-05 | 1985-12-05 | Sulphur trioxide absorption tower and process |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA1254365A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015054805A (en) * | 2013-09-13 | 2015-03-23 | 住友金属鉱山株式会社 | Method of drying sulfuric acid raw material gas |
| CN110217760A (en) * | 2019-05-23 | 2019-09-10 | 北京科技大学 | A kind of desulphurization waste liquid of coke oven gas relieving haperacidity preparation process |
-
1985
- 1985-12-05 CA CA000496982A patent/CA1254365A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015054805A (en) * | 2013-09-13 | 2015-03-23 | 住友金属鉱山株式会社 | Method of drying sulfuric acid raw material gas |
| CN110217760A (en) * | 2019-05-23 | 2019-09-10 | 北京科技大学 | A kind of desulphurization waste liquid of coke oven gas relieving haperacidity preparation process |
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