Process for the desulfurization of a crude gas containing H.sub.

Chemistry of inorganic compounds – Sulfur or compound thereof – Elemental sulfur

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4235741, 423220, 423222, 423224, 4232421, B01D 5348, B01D 5350, B01D 5352

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active

056289774

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BRIEF SUMMARY
BACKGROUND OF THE INVENTION

The invention relates to a process for the desulfurization of a crude gas stream containing at least H.sub.2 S in a Claus plant, afterburning of the Claus waste gas, and gas washing (scrubbing) of the waste gas from the afterburning to remove SO.sub.2, in which case SO.sub.2 recovered by the gas scrubbing is recycled to a point before the Claus plant.
Claus plants are widely used to recover elementary sulfur from gas streams containing H.sub.2 S. In this connection, a part of the H.sub.2 S is combusted to SO.sub.2 in a Claus reactor. SO.sub.2 and any remaining H.sub.2 S are reacted to form elementary sulfur and water in catalytic/thermal reactors corresponding to the Claus furnace. Claus plants have proven themselves very well in practice. But the degree of desulfurization that can be achieved with a clean Claus plant (depending on design and operation, between 90% and 97% of crude gas sulfur) does not satisfy today's requirements for reducing sulfur emissions to the atmosphere. To increase the degree of desulfurization and thus to reduce sulfur emissions, additional plant facilities downstream from the Claus plant are necessary for further treatment of the Claus waste gas. This further treatment of the Claus waste gas is usually referred to as "tail gas treatment."
A known process variant calls, for example, for the continuation of the reaction of the bound sulfur in elementary sulfur, which is incomplete in the Claus plant. In downstream catalysts (additional catalytic Claus stages), the reaction to sulfur continues corresponding to thermodynamic equilibrium at a reduced temperature level below the dew point of sulfur (sub-dew-point process), and simultaneously elementary sulfur is adsorbed on the catalyst. In this way, several reactors are periodically regenerated or switched to adsorption. Only by careful adjustment of the purge gas composition during regeneration can early deactivation of the catalyst be avoided. Contaminated, sulfur-containing gases must, if they cannot be handled in the Claus plant, be disposed of in some other way. Sulfur components COS and CS.sub.2 carried by the Claus waste gas are hydrolyzed to H.sub.2 S and CO.sub.2 to only a small extent and thus increase the sulfur burden in the waste gases. Spent catalysts must be disposed of. With such processes, degrees of desulfurization of up to 99.6% are achieved with relatively low operating and investment costs or up to 99.8% are achieved with considerably increased costs.
Another variant (direct oxidation process) for further treatment of the Claus waste gas comprises the hydrogenation of all sulfur compounds that are also contained in the Claus waste gas into H.sub.2 S. H.sub.2 S that is produced is chemically bonded by an aqueous absorption agent in an oxidative scrubbing or separated in a water-separation stage with catalytic oxidation. The oxidative scrubbing makes a sulfur yield of 99.9% possible, but with very high operating and investment costs. In the case of the catalytic-oxidative process, the degree of desulfurization remains limited to a maximum of 99.8% due to thermodynamic factors.
The so-called recycling processes, which all together comprise a gas scrubbing, teach a third variant of the further treatment of Claus waste gases. In this case, however, the Claus waste gas must first be completely hydrogenated or oxidized. When the Claus waste gas is hydrogenated, the resulting H.sub.2 S is scrubbing out in a chemical absorption step. When the scrubbing agent is regenerated, H.sub.2 S is released in concentrated form and can be fed to the Claus plant. For the reduction of H.sub.2 S, gases with hydrogen, carbon monoxide, or gas mixtures consisting of these substances are used. The degree to which the sulfur compounds are reacted into H.sub.2 S depends on the activity of the catalyst. During reaction to H.sub.2 S, COS can occur in the presence of carbon--for example in the form of CO--which is to be reacted separately. The reaction to H.sub.2 S requires an excess of reducing gas, so that dependin

REFERENCES:
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patent: 4632819 (1986-12-01), Fischer et al.
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Sander et al. "Sulfur, Sulfur Dioxide & Sulfuric Acid" (1984) British Sulfur Corp., London G.B., pp. 56-59 no month.
Heisel et al. "DAS Clintox-Verfahren zur Reinigung von Claus-Abgasen" (1989) Linde Berichte Aus Technik und Wissenschaft No. 63 Wiesbaden DE, pp. 13-15 (no month).

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