JPS54123591A - Exhaust gas treating method - Google Patents
Exhaust gas treating methodInfo
- Publication number
- JPS54123591A JPS54123591A JP3113078A JP3113078A JPS54123591A JP S54123591 A JPS54123591 A JP S54123591A JP 3113078 A JP3113078 A JP 3113078A JP 3113078 A JP3113078 A JP 3113078A JP S54123591 A JPS54123591 A JP S54123591A
- Authority
- JP
- Japan
- Prior art keywords
- soln
- exhaust gas
- gas
- contg
- salt
- 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.)
- Pending
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/20—Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
Landscapes
- Treating Waste Gases (AREA)
Abstract
PURPOSE: To remove SO2 at a high rate as well as to efficiently remove NO a high denitration rate by contacting NOx-contg. exhaust gas to an aq. NH3 soln. of a specific pH value contg. a reducing substance and a Co salt as an absorbing soln.
CONSTITUTION: Exhaust gas is contacted to the following absorbing soln. at ordinary temp.Wabout 80°C: an aq. soln. of pH≥6 obtd. by adding a Co salt to an aq. NH3 soln. contg. a reducing substance such as thiosulfate or thiocyanate, or an aq. soln. of pH≥6 obtd. by injecting NH3 into NH3 or Na type waste liquor used to desulfurize coke oven gas and adding a Co salt. The concn. of Co2+ ranges from 10-4 g ion/l to saturation solubility, that of SCN- from 0.01 mol/l to saturation solubility, and that of S2O3 2+ from 0.01 mol/l to saturation solubility. Since NO inexhaust gas can be oxidized with O2 in the gas and removed at a high rate without using O3 and ClO2, this method is economical.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3113078A JPS54123591A (en) | 1978-03-20 | 1978-03-20 | Exhaust gas treating method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3113078A JPS54123591A (en) | 1978-03-20 | 1978-03-20 | Exhaust gas treating method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS54123591A true JPS54123591A (en) | 1979-09-25 |
Family
ID=12322832
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3113078A Pending JPS54123591A (en) | 1978-03-20 | 1978-03-20 | Exhaust gas treating method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS54123591A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006061907A (en) * | 2005-09-08 | 2006-03-09 | Hitachi Zosen Corp | Formation suppressant and formation suppressing method of chlorinated aromatic compound |
-
1978
- 1978-03-20 JP JP3113078A patent/JPS54123591A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006061907A (en) * | 2005-09-08 | 2006-03-09 | Hitachi Zosen Corp | Formation suppressant and formation suppressing method of chlorinated aromatic compound |
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