DE2213579B1 - METHOD FOR CATALYTIC CONVERSION OF GASES WITH HIGH CONTENT AT SO LOW 2 - Google Patents
METHOD FOR CATALYTIC CONVERSION OF GASES WITH HIGH CONTENT AT SO LOW 2Info
- Publication number
- DE2213579B1 DE2213579B1 DE19722213579 DE2213579A DE2213579B1 DE 2213579 B1 DE2213579 B1 DE 2213579B1 DE 19722213579 DE19722213579 DE 19722213579 DE 2213579 A DE2213579 A DE 2213579A DE 2213579 B1 DE2213579 B1 DE 2213579B1
- Authority
- DE
- Germany
- Prior art keywords
- gases
- contact
- stream
- 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.)
- Granted
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
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 Gasmengen ebenfalls praktisch konstant bleiben und dadurch ein optimaler und einfacher Betrieb möglich ist. Außerdem können Schwankungen in der Gaszusammensetzung des Stromes Λ weitgehend ausgeglichen werden.The advantages of the invention are that when the catalyst is inactivated, the conversion to SO 3 is kept practically constant, the amounts of gas also remain practically constant, and optimal and simple operation is thereby possible. In addition, fluctuations in the gas composition of the stream Λ can be largely compensated for.
Hierzu 1 Blatt Zeichnungen1 sheet of drawings
f COPYf COPY
Claims (1)
gekennzeichnet, daß mindestens ein Teil- Diese Aufgabe wird erfindungsgemäß dadurchis admixed and the gases are intercooled 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
SO2-Gehalt bis zu etwa 11% kommt die Reaktion .When converting SO 2 -containing gases to contact tray 1 α to 1 d 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. A substream C of the stream B This light-off temperature is, for example, in the case of cata- lysts. It is passed into the absorber4 and freed from SO 3 there in a regulated one on the basis of vanadium pentoxide (V 2 O 5 ) depending on the amount. The stream Ό leaving the absorber 4 according to its composition and method of manufacture at 40 is passed into the mixing device 5 at about 400 to 450 ° C. During the conversion of SO 2 , where it is mixed with the stream. 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).
With a SO 2 content of up to about 11%, the reaction occurs.
höherem SO2-Gehalt steigt die Temperatur weiter, ,-Q0, ~qSO 2 + Va O 2 ^ SO 3 is achieved. For gases with a composition of
With higher SO 2 content, the temperature rises further,, -Q 0 , ~ q
Umsetzung von SO2 zu SO3, so daß bei entsprechen- Im zweiten Jahr werden im Absorber 4 30 % SO3 Gases containing SO 2 before being used in the first 55 In the first year, no SO 3 ab contact tray SO 3 -containing gases will be mixed in in the absorber 4. sorbed. The stream £ then contains 3.37% SO 3 , the admixture of the SO 3 has the effect of braking ; the stream B contains 22.14% SO 2 and 37.14% SO 3 .
Conversion of SO 2 to SO 3 , so that in the second year there are 30% SO 3 in the absorber 4
entsprechend nach und der Gasumsatz zu SO3 ver- Der Gesamtumsatz der Anlage bleibt praktischBecomes inactive over time, leaves the reaction 65 absorbed. Stream £ then contains no SO 3 , the rate of the reaction SO 2 + V2 O 2 ^ SO 3. Stream B contains 23.03% SO 2 and 34.54% 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 | |
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 |
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 |
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 true DE2213579B1 (en) | 1973-06-20 |
DE2213579C2 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 FR FR7309876A patent/FR2176920B3/fr not_active Expired
- 1973-03-20 ES ES412844A patent/ES412844A1/en not_active Expired
- 1973-03-20 SE SE7303911A patent/SE382623B/en unknown
Also Published As
Publication number | Publication date |
---|---|
CA982324A (en) | 1976-01-27 |
JPS4913097A (en) | 1974-02-05 |
FR2176920A1 (en) | 1973-11-02 |
DE2213579C2 (en) | 1974-01-24 |
ES412844A1 (en) | 1976-01-01 |
SE382623B (en) | 1976-02-09 |
ZA731275B (en) | 1974-05-29 |
AU472074B2 (en) | 1976-05-13 |
FR2176920B3 (en) | 1976-03-19 |
AU5269973A (en) | 1974-08-29 |
GB1397044A (en) | 1975-06-11 |
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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 |