Patent classifications
C01B17/765
METHOD AND PLANT DESIGN FOR REDUCTION OF START-UP SULFUR OXIDE EMISSIONS IN SULFURIC ACID PRODUCTION
The invention is a method and a sulfuric acid plant design for reduction of start-up SO.sub.2, SO.sub.3 and H.sub.2SO.sub.4 emissions in sulfuric acid production, in which SO2 is converted to SO.sub.3 in n successive catalyst beds, where n is an integer >1. The final catalytic beds are used as absorbents for SO.sub.2 to SO3 during the start-up procedure, and one or more of the m beds downstream the first bed are purged, either separately or simultaneously, with hot gas, where m is an integer >1 and m<n, during the previous shut-down. Also, one separate purge with hot gas is used on the final bed.
SINGLE CONTACT, SINGLE ABSORPTION SYSTEM FOR PRODUCING SULFURIC ACID WITH HIGH CONVERSION EFFICIENCY
Commercial production of sulfuric acid is almost entirely accomplished nowadays using the contact process. And the trend is to increase conversion efficiency and reduce emissions of unconverted sulfur dioxide. By using a special combination of contact catalyst beds, a single contact single absorption (SCSA) system can be engineered to achieve the conversion and emission capabilities of conventional double contact double absorption systems. Thus, the complexity and cost of incorporating a second absorption tower and associated heat exchanger in the system can be omitted. In the SCSA system, the initial catalyst bed or beds comprise vanadium oxide catalyst and the last catalyst bed or beds comprise platinum catalyst operating at a much lower temperature than the initial beds.
SINGLE CONTACT, SINGLE ABSORPTION SYSTEM FOR PRODUCING SULFURIC ACID WITH HIGH CONVERSION EFFICIENCY
Commercial production of sulfuric acid is almost entirely accomplished nowadays using the contact process. And the trend is to increase conversion efficiency and reduce emissions of unconverted sulfur dioxide. By using a special combination of contact catalyst beds, a single contact single absorption (SCSA) system can be engineered to achieve the conversion and emission capabilities of conventional double contact double absorption systems. Thus, the complexity and cost of incorporating a second absorption tower and associated heat exchanger in the system can be omitted. In the SCSA system, the initial catalyst bed or beds comprise vanadium oxide catalyst and the last catalyst bed or beds comprise platinum catalyst operating at a much lower temperature than the initial beds.
Process and plant for improved energy-efficient production of sulfuric acid
The invention describes a process for producing sulfuric acid by catalytic oxidation of SO.sub.2 to SO.sub.3 and subsequent absorption of the SO.sub.3 in sulfuric acid, wherein the SO.sub.3 is introduced into a first absorption stage (primary absorber) and at least partly absorbed there in concentrated sulfuric acid, wherein the SO.sub.3 not absorbed in the first absorption stage is supplied to a second absorption stage (secondary absorber) for the further absorption in concentrated sulfuric acid, and wherein the sulfuric acid is cooled after passing through the two absorption stages. The cooling of the sulfuric acid is effected in at least two heat exchangers connected in parallel, wherein one of the at least two heat exchangers is operated as partial evaporator and is cooled with boiler feed water/steam and the other one is cooled with cooling water and operated as pure acid cooler.
METHOD AND DEVICE FOR PRODUCING SULFURIC ACID
In a production mode a process for preparing sulfuric acid may involve oxidizing sulfur to sulfur dioxide in a first oxidation stage, and catalytically oxidizing the sulfur dioxide to sulfur trioxide in a second oxidation stage. The sulfur trioxide may be absorbed in at least one absorption stage. In the production mode, process gases from a last of the at least one absorption stage with respect to a flow direction are discharged. In a standby mode of the process, at least one heating stage for heating the process gases is connected. The process gases exiting from the at least one absorption stage are conveyed to the heating stage, and the process gases are circulated via the heating stage, the second oxidation stage, and the absorption stage.
CATALYTIC REACTOR
A catalytic reactor may have at least one reactor module and a shell that extends about a reactor center axis. The reactor module may include a gas distribution chamber, a gas collection chamber, and a catalyst. The gas distribution chamber may be connected to a shell-side gas feed. The gas collection chamber may be connected to a shell-side gas discharge. A catalyst bed between the distribution and collection chambers may extend transversely to the reactor center axis. The gas distribution and collection chambers are bounded by the catalyst bed and reactor walls. The gas feed either opens into the gas distribution chamber on the shell side or is connected to a pipe length that extends towards the reactor center axis and opens into the gas distribution chamber in the region of the reactor center axis. A height parallel to the reactor center axis of the gas distribution chamber reduces towards the reactor center axis starting from a mouth of the gas feed in the case of a shell-side connection.
CATALYTIC REACTOR
A catalytic reactor may have at least one reactor module and a shell that extends about a reactor center axis. The reactor module may include a gas distribution chamber, a gas collection chamber, and a catalyst. The gas distribution chamber may be connected to a shell-side gas feed. The gas collection chamber may be connected to a shell-side gas discharge. A catalyst bed between the distribution and collection chambers may extend transversely to the reactor center axis. The gas distribution and collection chambers are bounded by the catalyst bed and reactor walls. The gas feed either opens into the gas distribution chamber on the shell side or is connected to a pipe length that extends towards the reactor center axis and opens into the gas distribution chamber in the region of the reactor center axis. A height parallel to the reactor center axis of the gas distribution chamber reduces towards the reactor center axis starting from a mouth of the gas feed in the case of a shell-side connection.
PROCESS AND APPARATUS FOR PREPARING SULFUR TRIOXIDE FROM SULFUR DIOXIDE
A process for the catalytic conversion of sulfur dioxide to sulfur trioxide to increase sulfuric acid regeneration from a spent sulfuric acid stream or other sulfur-containing stream includes replacing at least a portion of the atmospheric air typically used to oxidize sulfur dioxide to sulfur trioxide with oxygen by introducing oxygen-enriched air and/or pure oxygen feed streams into the process. A related apparatus for use in the process is also provided for catalytic conversion of sulfur dioxide to sulfur trioxide.
PROCESS AND APPARATUS FOR PREPARING SULFUR TRIOXIDE FROM SULFUR DIOXIDE
A process for the catalytic conversion of sulfur dioxide to sulfur trioxide to increase sulfuric acid regeneration from a spent sulfuric acid stream or other sulfur-containing stream includes replacing at least a portion of the atmospheric air typically used to oxidize sulfur dioxide to sulfur trioxide with oxygen by introducing oxygen-enriched air and/or pure oxygen feed streams into the process. A related apparatus for use in the process is also provided for catalytic conversion of sulfur dioxide to sulfur trioxide.
Method for the catalytic removal of sulphur dioxide from waste gases
The present invention relates to a method for the catalytic removal of sulfur dioxide from waste gases in two reactors, wherein the first reactor is charged with an activated carbon catalyst. The method comprises: a. provision of a waste gas with a water content of less than 1 g H.sub.2O/Nm.sup.3 and an SO.sub.2 content of at least 5 ppm, b. introduction of the waste gases into a first reactor, c. catalytic conversion of the SO.sub.2 into gaseous SO.sub.3 in the first reactor by the activated carbon catalyst, wherein catalytic conversion on the activated carbon catalyst proceeds at a temperature of below 100 C., d. introduction of the prepurified waste gases from the first reactor into a second reactor, e. conversion of the SO.sub.3 with water into H.sub.2SO.sub.4 in the second reactor.