FIELD: sulfur and hydrogen peroxide production. SUBSTANCE: hydrogen sulfide-containing gas is brought in contact with 2,3-dialkyl-substituted naphtoquinone in presence of amine catalyst dissolved in hydrophobic organic solvent system to produce corresponding quinhydrone and insoluble elementary sulfur. Total number of carbon atoms in alkyl substituents ranges advantageously from 2 to 6. Most appropriate compounds are dimethyl- and/or ethyl/methylnaphtoquinones. Preferable pH value is 9 to 11.5 and preferable solvent systems are mixtures of aromatic hydrocarbons with alifatic esters, such as methyl cyclohexanolacetate, or dialkylcarbinols, such as diisobutylcarbinol. Naphtoquinones react with H2S substantially faster than antraquinone and tetrahydpoanthraquinone compounds which are known reagents with H2Or. Insoluble sulfur may be removed as reaction product, whereas solution containing reduced naphtoquinhydrone may be brought in contact with oxygen-containing gas to produce hydrogen peroxide and produce back naphtoquinone. Extracted with water to remove H2S, solution may be reused in contact with another H2S-containing gas. EFFECT: enhanced hydrogen sulfide conversion process. 16 cl
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Authors
Dates
1997-12-20—Published
1994-01-26—Filed