A process and a process plant for production of elemental sulfur from a feedstock gas including from 15 vol % to 100 vol % H2S and a stream of sulfuric acid, the process including a) providing a Claus reaction furnace feed stream with a substoichiometric amount of oxygen, b) directing s to a reaction furnace operating at elevated temperature, c) cooling, d) directing to contact a material catalytically active in the Claus reaction, e) withdrawing a Claus tail gas and elemental sulfur, f) directing to a means for sulfur oxidation, g) directing to contact a material catalytically active in SO2 oxidation to SO3, h) converting to concentrated sulfuric acid, i) recycling to the Claus reaction furnace, wherein an amount of combustibles, in the Claus tail gas, is oxidized in the presence of a material catalytically active in sulfur oxidation, at an inlet temperature below 400° C.

A revamp process for modifying a sulfur abatement plant including a Claus process plant, the Claus process plant including a Claus reaction furnace and one or more Claus conversion stages, each Claus conversion stage including a conversion reactor and a means for elemental sulfur condensation, and a means of Claus tail gas oxidation configured for receiving a Claus tail gas from said Claus process plant and configured for providing an oxidized Claus tail gas, the process revamp including: a) providing a sulfuric acid producing tail gas treatment plant producing sulfuric acid, and b) providing a means for transferring an amount or all of the sulfuric acid produced in said sulfuric acid producing tail gas treatment plant to said Claus reaction furnace, wherein the moles of sulfur in the transferred sulfuric acid relative to the moles of elemental sulfur withdrawn from the Claus process plant is from 3% to 25%.

Disclosed is a process system and a process for converting the sulfur-containing flue gas into the sulfuric acid. The process system comprises: a flue gas preheater, which for preheating the sulfur-containing flue gas to 15˜30° C. above its dew point, and the flue gas preheater has a glass tube as a heat exchange tube; a flue gas fan for boosting the pressure of the preheated acid process gas and transporting one part of which to a combustion furnace, and the other part of which to a process gas steam heater; a sulfuric acid steam condenser for condensing SO.sub.3 generated by the combined reactor into sulfuric acid. The device of the present invention can resist the fluctuation of SO.sub.2 concentration in the feed gas, and can realize considerable economic benefits and rational utilization of energy.

Improved systems and methods are disclosed for producing sulfur dioxide using oxygen and submerged combustion. By incorporating a vapour phase combusting step in addition to the submerged combusting step, the downstream sulfur condenser may be made substantially smaller with reduced complexity and cost. Further, energy recovery is simplified and improved.

A method and system for cooling sulfuric acid aqueous solutions (H.sub.2SO.sub.4) belonging to the field of chemical processes, which is part of a contact process for production of sulfuric acid with or without energy recovery. The method comprises absorption of SO.sub.3, which produces heated concentrated sulfuric acid and indirectly cooling the hot acid. The method uses a sulfuric acid-inert coolant. A cooling step comprises an intermediate indirect acid-fluid cooling and a second fluid-water or fluid indirect cooling stepthird fluid, wherein when the process is of the type with energy recovery. A third step includes energy recovery, steam generation. A system to perform the method, which works next to the SO.sub.3 absorption tower comprises an acid cooling loop consisting of an intermediate acid-fluid heat exchanger; a second fluid-water heat exchanger, and when the process is of the type with energy recovery, said equipment further includes a steam generation boiler.

A process for preparing sulfuric acid may involve oxidizing sulfur to sulfur dioxide by way of dried air in a first oxidation stage. The sulfur dioxide may then be oxidized to sulfur trioxide in a second oxidation stage. The sulfur trioxide may be absorbed by sulfuric acid in at least one absorption stage. Further, heated sulfuric acid may be drawn off from the absorption stage and used for generating steam. Process gas from an intermediate absorption stage may be recycled to the second oxidation stage and, in some cases, a final absorption stage after the process gas flows through the second oxidation stage.

A process for preparing sulfuric acid may involve oxidizing sulfur to sulfur dioxide by way of dried air in a first oxidation stage. The sulfur dioxide may then be oxidized to sulfur trioxide in a second oxidation stage. The sulfur trioxide may be absorbed by sulfuric acid in at least one absorption stage. Further, heated sulfuric acid may be drawn off from the absorption stage and used for generating steam. Process gas from an intermediate absorption stage may be recycled to the second oxidation stage and, in some cases, a final absorption stage after the process gas flows through the second oxidation stage.

In a method for cooling of process gas between catalytic layers or beds in a sulfuric acid plant, in which sulfuric acid is produced from feed gases containing sulfurous components like SO.sub.2, H.sub.2S, CS.sub.2 and COS or liquid feeds like molten sulfur or spent sulfuric acid, one or more boilers, especially water tube boilers, are used instead of conventional steam superheaters to cool the process gas between the catalytic beds in the SO.sub.2 converter of the plant. Thereby a less complicated and more cost efficient heat exchanger layout is obtained.

Sulfur trioxide is produced from a feed stream comprising sulfur-containing compounds and dissolved metals, such as alkali metals, in a plant comprising an incineration furnace, a waste heat boiler, a dilution air heater, a dust removal absorber and an SO.sub.2 converter. The plant may further comprise a sulfuric acid condenser for the production of sulfuric acid.

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.