Organic sulfur compounds contained in refinery off gas streams having either high or low concentrations of olefins are converted to hydrogen sulfides which can be then be removed using conventional amine treating systems. The process uses a catalytic reactor with or without a hydrotreater depending on the olefin concentration of the off gas stream. The catalytic reactor operates in a hydrogenation mode or an oxidation mode to convert a majority of organic sulfur compounds into hydrogen sulfides.

Systems and methods use bimetallic alloy particles for converting hydrogen sulfide (H.sub.2S) to hydrogen (H.sub.2) and sulfur (S), typically during multiple operations. In a first operation, metal alloy composite particles can be converted to a composite metal sulfide. In a second operation, composite metal sulfide from the first operation can be regenerated back to the metal alloy composite particle using an inert gas stream. Pure, or substantially pure, sulfur can also be generated during the second operation.

Organic sulfur compounds contained in refinery off gas streams having either high ort low concentrations of olefins are converted to hydrogen sulfides which can be then be removed using conventional amine treating systems. The process uses a catalytic reactor with or without a hydrotreater depending on the olefin concentration of the off gas stream. The catalytic reactor operates in a hydrogenation mode or an oxidation mode to convert a majority of organic sulfur compounds into hydrogen sulfides.

The present application relates to a process for treating the off gas from a carbon black process, said process comprising the steps of: providing an off gas from a carbon black process, reacting said off gas in a first reaction step forming water and S, and condensing the S at a temperature Tcon where S is in a liquid phase and the water is in gas form thereby achieving a gaseous stream comprising water and a liquid stream comprising S, and wherein the first reaction step is carried out over a monolith catalyst.

The invention describes a filter medium (10), in particular for an air filter, in particular an interior air filter or for a fuel cell, including at least three active layers: a catalytic active layer (12) comprising catalytic activated carbon particles (12a), a second active layer (14) comprising impregnated or catalytic activated carbon particles (14a), a third active layer (16) comprising impregnated or catalytic activated carbon particles (16a), wherein at least one active layer comprises impregnated activated carbon particles and the three active layers (12, 14, 16) differ from one another. The invention further discloses a filter media body including the filter medium; a filter element including the filter media body or the filter medium; an air filter including the filter element or the filter media body or the filter medium, and a production method for producing the filter medium.

Disclosed is a catalyst suitable for the catalytic oxidative cracking of a H.sub.2S-containing gas stream. The catalyst comprises at least one or more active metals selected from the group consisting of iron, cobalt, and nickel, supported by a carrier comprising ceria and alumina. The active metal is preferably in the form of its sulphide. Also disclosed is a method for the production of hydrogen from a H.sub.2S-containing gas stream, comprising subjecting the gas stream to catalytic oxidative cracking so as to form H.sub.2 and S.sub.2, using a catalyst in accordance with any one of the composition claims.

The invention relates to an installation and a method for treating hydrogen sulphide. In particular, the invention relates to an installation and a method comprising at least one system for oxidizing hydrogen sulfide to sulfur (S) and water (H.sub.2O) with a solid reagent and at least one oxidizing system with an agent for oxidizing the solid reagent present in the reduced state, wherein the system of oxidizing the hydrogen sulfide to sulfur and the system for oxidizing the solid reagent, are so arranged that the hydrogen sulfide is not brought into contact with the agent oxidizing the solid reagent.

A supported catalyst having catalytic species including molybdenum as well as cobalt and/or vanadium as a promoter disposed on a support material containing zeolite modified with titanium dioxide. Various methods of preparing and characterizing the supported catalyst are disclosed. The utilization of the catalyst in treating a hydrocarbon feedstock containing sulfur compounds (e.g. dibenzothiophene) to produce a desulfurized hydrocarbon stream is also provided.

Recovering helium from a gaseous stream includes contacting an acid gas removal membrane with a gaseous stream to yield a permeate stream and a residual stream, removing a majority of the acid gas from the residual stream to yield a first acid gas stream and a helium depleted clean gas stream, removing a majority of the acid gas from the permeate stream to yield a second acid gas stream and a helium rich stream, and removing helium from the helium rich stream to yield a helium product stream and a helium depleted stream. A helium removal system for removing helium from a gaseous stream including hydrocarbon gas, acid gas, and helium includes a first processing zone including a first acid gas removal unit, a second processing zone including a second acid gas removal unit, a third processing zone, and a helium purification unit.

The invention relates to a process for removing hydrogen sulfide and carbon dioxide from a feed gas stream. H2S in the feed gas stream is converted to elemental sulfur in a Claus unit. At least a part of the gas stream obtained is contacted with an aqueous lean absorbing medium in an absorption zone at a pressure between 0.9 and 2 bara. The aqueous lean absorbing medium used comprises one or more amines chosen from: a polyamine in the absence of tertiary amine functionalities having a pKa sufficient to neutralize carbamic acid, the polyamine having at least one primary amine functionality having a pKa smaller than 10.0 at 25 C., a polyamine in the absence of tertiary amine functionalities having a pKa sufficient to neutralize carbamic acid, the polyamine having at least one secondary amine functionality having a pKa for each sorbing nitrogen smaller than 10.0 at 25 C. The process is improved as compared to a process involving Claus off-gas treatment with (activated) MDEA. Effective CO2 removal is achieved while at the same time a simplified line-up with less equipment can be used.