A two or particularly three-phase process, and corresponding apparatus, desulfurizes sour hydrocarbon gas, e.g., natural gas, generally better than known, using a fixed-bed, two-phase processes in terms of the amount of H.sub.2S scavenged and the breakthrough time of H.sub.2S. The three-phase process is effective in scavenging H.sub.2S at ambient temperature and pressure, using a copper salt catalyst impregnated on alumina or other generally inert support, which is regenerable.

A two or particularly three-phase process, and corresponding apparatus, desulfurizes sour hydrocarbon gas, e.g., natural gas, generally better than known, using a fixed-bed, two-phase processes in terms of the amount of H.sub.2S scavenged and the breakthrough time of H.sub.2S. The three-phase process is effective in scavenging H.sub.2S at ambient temperature and pressure, using a copper salt catalyst impregnated on alumina or other generally inert support, which is regenerable.

A two or particularly three-phase process, and corresponding apparatus, desulfurizes sour hydrocarbon gas, e.g., natural gas, generally better than known, using a fixed-bed, two-phase processes in terms of the amount of H.sub.2S scavenged and the breakthrough time of H.sub.2S. The three-phase process is effective in scavenging H.sub.2S at ambient temperature and pressure, using a copper salt catalyst impregnated on alumina or other generally inert support, which is regenerable.

A two or particularly three-phase process, and corresponding apparatus, desulfurizes sour hydrocarbon gas, e.g., natural gas, generally better than known, using a fixed-bed, two-phase processes in terms of the amount of H.sub.2S scavenged and the breakthrough time of H.sub.2S. The three-phase process is effective in scavenging H.sub.2S at ambient temperature and pressure, using a copper salt catalyst impregnated on alumina or other generally inert support, which is regenerable.

In a process for the removal of soot from a sulfurous gas stream, a process gas containing O.sub.2 and more than 500 ppm SO.sub.2 and/or SO.sub.3 together with soot is brought into contact with a VK type catalyst in a reactor, said catalyst comprising vanadium pentoxide (V.sub.2O.sub.5), sulfur in the form of sulfate, pyrosulfate, tri- or tetrasulfate and one or more alkali metals, such as Na, K, Rb or Cs, on a porous carrier, preferably a silicon dioxide carrier.

A novel catalyst, a use thereof and a method for treating PCB inked waste by using the same are disclosed. The catalyst of the present disclosure is represented by the following formula (I):

[M(O).sub.a].sup.m+X.sup.n(I)

herein M, X, a, m and n are defined in the specification.

A novel catalyst, a use thereof and a method for treating PCB inked waste by using the same are disclosed. The catalyst of the present disclosure is represented by the following formula (I):

[M(O).sub.a].sup.m+X.sup.n(I)

herein M, X, a, m and n are defined in the specification.

Methods of preparing a second high-efficiency, rhenium-promoted silver catalyst for producing alkylene oxide from an alkylene based on a first catalyst are disclosed and described. In accordance with the disclosed methods, the first and second catalysts include at least one promoter that includes a rhenium promoter. The target catalyst concentrations of one or more promoters of the at least one promoter on the second catalyst are determined based on the values of a catalyst reference property for the two catalysts and the concentration of the one or more promoters of the at least one promoter on the first catalyst. Suitable catalyst reference properties include carrier specific surface area and silver specific surface area. Reaction systems utilizing the first and second catalysts are also described.

Methods of preparing a second high-efficiency, rhenium-promoted silver catalyst for producing alkylene oxide from an alkylene based on a first catalyst are disclosed and described. In accordance with the disclosed methods, the first and second catalysts include at least one promoter that includes a rhenium promoter. The target catalyst concentrations of one or more promoters of the at least one promoter on the second catalyst are determined based on the values of a catalyst reference property for the two catalysts and the concentration of the one or more promoters of the at least one promoter on the first catalyst. Suitable catalyst reference properties include carrier specific surface area and silver specific surface area. Reaction systems utilizing the first and second catalysts are also described.

Hydroxypropionic acid, hydroxypropionic acid derivatives, or mixtures thereof are dehydrated using a catalyst and a method to produce bio-acrylic acid, acrylic acid derivatives, or mixtures thereof. A method to produce the dehydration catalyst is also provided.