DE2213579C2 - Process for the catalytic conversion of gases with a high content of SO deep 2 - Google Patents
Process for the catalytic conversion of gases with a high content of SO deep 2Info
- Publication number
- DE2213579C2 DE2213579C2 DE2213579A DE2213579A DE2213579C2 DE 2213579 C2 DE2213579 C2 DE 2213579C2 DE 2213579 A DE2213579 A DE 2213579A DE 2213579 A DE2213579 A DE 2213579A DE 2213579 C2 DE2213579 C2 DE 2213579C2
- Authority
- DE
- Germany
- Prior art keywords
- gases
- stream
- contact
- absorber
- conversion
- 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
- 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
- C01B17/765—Multi-stage SO3-conversion
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Catalysts (AREA)
- Gas Separation By Absorption (AREA)
Description
Der Strom B wird in bekannter Weise weiterverarbeitet. Stream B is processed further in a known manner.
Die Vorteile der Erfindung bestehen darin, daß bei der Inaktivierung des Katalysators der Umsatz zu SO3 praktisch konstant gehalten wird, die GasThe advantages of the invention are that when the catalyst is inactivated, the conversion to SO 3 , the gas, is kept practically constant
mengen ebenfalls praktisch konstant bleiben und dadurch ein opiimaler und einfacher Betrieb möglich ist. Außerdem können Schwankungen in der Gaszusammensetzung des Stromes A weitgehend ausgeglichen werden.quantities also remain practically constant and thus an optimal and simple operation is possible. In addition, fluctuations in the gas composition of stream A can be largely compensated for.
Hierzu 1 Blatt Zeichnungen1 sheet of drawings
Claims (1)
gekennzeichnet, daß mindestens ein Teil- Diese Aufgabe wird erfindungsgemäß dadurchis admixed and the gases are cooled between contact io reduction of the conversion to SO 3 due to inhorden, thereby preventing activation of the contact mass,
characterized in that at least one part of this object is achieved according to the invention
SO.,-Gehalt bis zu etwa 11 Vo kommt die Reaktion .When converting SO, -hahigen gases to contact tray 1 α to 1 rf and the intermediate cooler 2 a SO 3 with subsequent sulfuric acid production, 35 to 2 c. The stream B leaving the contact vessel 1, the catalyst mass through the gas first of all to the gas partially converted to SO 3 , is brought to the so-called light-off temperature. Cooler 3 cooled down. A Teilstrcn C of the stream B This light-off temperature is z. B. in the case of cata- lysts is passed into the absorber 4 and freed there in regulated gates based on vanadium pentoxide (V 2 O.) ic ter amount of SO 3. The stream D leaving the absorber 4 at 40 ° C according to its composition and method of manufacture is passed into the mixing device 5 at around 400 to 450 ° C. During the conversion of SO 2 , it is mixed with the stream A there. An increase in temperature occurs to SO 3 , since substream F of substream C can cause absorber 4, the reaction is exothermic. In the case of gases, deal with one (shown in dashed lines).
So., - content up to about 11 Vo the reaction occurs.
höherem SO2-Gehalt steigt die Temperatur weiter, ^q 0/ <jqSO 2 -t- Ά O 2 ^ SO S is reached. For gases with a composition of
With higher SO 2 content, the temperature continues to rise, ^ q 0 / <jq
Umsetzung von SO2 zu SO3, so daß bei entsprechen- Im zweiten Jahr werden im Absorber 4 30°/o SO3 SO., - containing gases before use in the first 55 In the first year, no SO., Ab contact tray SOj-containing oases will be mixed in in the absorber 4. sorbed. The stream E then contains 3.37 "-Ό SO ; i , der The admixture of the SO 3 causes a braking of the stream S contains 22.14" / o SO 2 and 37.14 0 O SO 3 .
Conversion of SO 2 to SO 3 , so that in the second year, 30% SO 3 are in the absorber 4
entsprechend nach und der Gasumsatz zu SO3 ver- Der Gesamtumsatz der Anlage bleibt praktischIn the course of time it becomes inactive, the reaction 65 is absorbed. Stream E then contains no SO 3 , the rate of the reaction is SO 2 + V 2 O 2 ^ SO., Stream B contains 23.03 Vo SO 2 and 34.54 Vo SO 3 .
accordingly gradually and the gas turnover to SO 3 The total turnover of the plant remains practically
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2213579A DE2213579C2 (en) | 1972-03-21 | 1972-03-21 | Process for the catalytic conversion of gases with a high content of SO deep 2 |
ZA731275A ZA731275B (en) | 1972-03-21 | 1973-02-22 | Process of catalytically reacting gases having a high so2 content |
AU52699/73A AU472074B2 (en) | 1972-03-21 | 1973-02-28 | Process of catalytically reacting gases having a high 80 2 content |
GB1036673A GB1397044A (en) | 1972-03-21 | 1973-03-02 | Process for catalytically reacting gases having a high sulphur dioxide content in a contact plant |
JP48031351A JPS4913097A (en) | 1972-03-21 | 1973-03-17 | |
SE7303911A SE382623B (en) | 1972-03-21 | 1973-03-20 | PROCEDURE FOR CATALYTIC SALES OF GAS WITH HIGH CONTENT OF SO? 712 IN CONTACT FACILITY |
CA166,979A CA982324A (en) | 1972-03-21 | 1973-03-20 | Process for catalytically reacting gases having a high so2 content |
FR7309876A FR2176920B3 (en) | 1972-03-21 | 1973-03-20 | |
ES412844A ES412844A1 (en) | 1972-03-21 | 1973-03-20 | Process for catalytically reacting gases having a high sulphur dioxide content in a contact plant |
US05/618,192 US3997655A (en) | 1972-03-21 | 1975-09-30 | Process for catalytically reacting gases having a high SO2 content |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2213579A DE2213579C2 (en) | 1972-03-21 | 1972-03-21 | Process for the catalytic conversion of gases with a high content of SO deep 2 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2213579B1 DE2213579B1 (en) | 1973-06-20 |
DE2213579C2 true DE2213579C2 (en) | 1974-01-24 |
Family
ID=5839568
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2213579A Expired DE2213579C2 (en) | 1972-03-21 | 1972-03-21 | Process for the catalytic conversion of gases with a high content of SO deep 2 |
Country Status (9)
Country | Link |
---|---|
JP (1) | JPS4913097A (en) |
AU (1) | AU472074B2 (en) |
CA (1) | CA982324A (en) |
DE (1) | DE2213579C2 (en) |
ES (1) | ES412844A1 (en) |
FR (1) | FR2176920B3 (en) |
GB (1) | GB1397044A (en) |
SE (1) | SE382623B (en) |
ZA (1) | ZA731275B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10249782A1 (en) | 2002-10-24 | 2004-05-06 | Outokumpu Oyj | Process and plant for the production of sulfuric acid from sulfur dioxide-rich gases |
-
1972
- 1972-03-21 DE DE2213579A patent/DE2213579C2/en not_active Expired
-
1973
- 1973-02-22 ZA ZA731275A patent/ZA731275B/en unknown
- 1973-02-28 AU AU52699/73A patent/AU472074B2/en not_active Expired
- 1973-03-02 GB GB1036673A patent/GB1397044A/en not_active Expired
- 1973-03-17 JP JP48031351A patent/JPS4913097A/ja active Pending
- 1973-03-20 CA CA166,979A patent/CA982324A/en not_active Expired
- 1973-03-20 SE SE7303911A patent/SE382623B/en unknown
- 1973-03-20 FR FR7309876A patent/FR2176920B3/fr not_active Expired
- 1973-03-20 ES ES412844A patent/ES412844A1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
AU5269973A (en) | 1974-08-29 |
FR2176920A1 (en) | 1973-11-02 |
GB1397044A (en) | 1975-06-11 |
SE382623B (en) | 1976-02-09 |
JPS4913097A (en) | 1974-02-05 |
ZA731275B (en) | 1974-05-29 |
ES412844A1 (en) | 1976-01-01 |
DE2213579B1 (en) | 1973-06-20 |
CA982324A (en) | 1976-01-27 |
AU472074B2 (en) | 1976-05-13 |
FR2176920B3 (en) | 1976-03-19 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
E77 | Valid patent as to the heymanns-index 1977 | ||
EHJ | Ceased/non-payment of the annual fee |