The invention relates to process for the manufacture or preparation of fluorinated benzene, in particular monofluorobenzene, in a vapor-phase fluorination process. The process of the invention, for example, can comprise a batch or continuous manufacture or preparation of fluorinated benzene, in particular monofluorobenzene, using hydrogen fluoride (HF) in gas phase as fluorination gas. Also, in this process of the invention, for example, fluorination catalysts are involved.

Disclosed is a combustion chamber (10) of the carbon dioxide supplier including: a combustion chamber (10) combusting a mixture of air and fuel; an air supply unit supplying an into the combustion chamber (10); and a fuel supply unit supply in a fuel to the combustion chamber (10). Representative Figure is FIG. 6.

A method is described of producing a catalyst-containing composite oxygen ion membrane and a catalyst-containing composite oxygen ion membrane in which a porous fuel oxidation layer and a dense separation layer and optionally, a porous surface exchange layer are formed on a porous support from mixtures of (Ln.sub.1xA.sub.x).sub.wCr.sub.1yB.sub.yO.sub.3 and a doped zirconia. Adding certain catalyst metals into the fuel oxidation layer not only enhances the initial oxygen flux, but also reduces the degradation rate of the oxygen flux over long-term operation. One of the possible reasons for the improved flux and stability is that the addition of the catalyst metal reduces the chemical reaction between the (Ln.sub.1xA.sub.x).sub.wCr.sub.1yB.sub.yO.sub.3 and the zirconia phases during membrane fabrication and operation, as indicated by the X-ray diffraction results.

A method is described of producing a catalyst-containing composite oxygen ion membrane and a catalyst-containing composite oxygen ion membrane in which a porous fuel oxidation layer and a dense separation layer and optionally, a porous surface exchange layer are formed on a porous support from mixtures of (Ln.sub.1xA.sub.x).sub.wCr.sub.1yB.sub.yO.sub.3 and a doped zirconia. Adding certain catalyst metals into the fuel oxidation layer not only enhances the initial oxygen flux, but also reduces the degradation rate of the oxygen flux over long-term operation. One of the possible reasons for the improved flux and stability is that the addition of the catalyst metal reduces the chemical reaction between the (Ln.sub.1xA.sub.x).sub.wCr.sub.1yB.sub.yO.sub.3 and the zirconia phases during membrane fabrication and operation, as indicated by the X-ray diffraction results.

The present invention relates to a process for treating, in a reactor containing a catalytic bed, a solid catalyst, said process comprising the steps of: a) implementing, in said reactor, a gas-phase catalytic reaction at a catalytic bed temperature T1 in the presence of a hydrogen halide or giving rise to the formation of a hydrogen halide, b) causing an inert gas to flow through the catalytic bed at a catalytic bed temperature T2 that is lower than T1, the temperature T2 being greater than 30 C.

A method comprising contacting a silica support with a titanium-containing solution to form a titanated silica support, wherein the titanium-containing solution comprises a solvent; a ligand comprising a glycol, a carboxylate, a peroxide, or a combination thereof; and a titanium compound having the formula Ti(acac).sub.2(OR).sub.2, wherein acac is acetylacetonate and wherein each R independently is ethyl, isopropyl, n-propyl, isobutyl, or n-butyl.

A catalyst comprising a carrier and a metals component impregnated in the carrier, the carrier comprising alumina; and the metals component comprising a first metals fraction and a second metals fraction, the first metals fraction comprising at least one metal selected from chromium, molybdenum, or tungsten, and the second metals fraction comprising at least two metals selected from cobalt, rhodium, iridium, nickel, palladium, or platinum, wherein the catalyst has a first pore volume of 0.28 to 0.45 mL/g for pores having a pore diameter of 12 nm to less than 16 nm, and a second pore volume of 0.15 to 0.28 mL/g for pores of 2.0 nm to less than 12.0 nm.

A sintered pelletized catalyst precursor comprising iron oxides, including haematite, and Cr.sub.2O.sub.3 and optionally one or more of Al.sub.2O.sub.3, ZnO, MnO.sub.2, MgO, and/or CuO, the pelletized catalyst precursor having an iron oxide content of 60 wt % to 95 wt %, when expressed as Fe.sub.2O.sub.3, and a Cr(VI) content of less than 0.1 wt %, is physically stable on ignition or when subjected to a reducing gas sufficient to reduce the haematite to magnetite.

Use of diverse biomass feedstock in a process for the recovery of target C5 and C6 alditols and target glycols via staged hydrogenation and hydrogenolysis processes is disclosed. Particular alditols of interest include, but are not limited to, xylitol and sorbitol. Various embodiments of the present invention synergistically improve overall recovery of target alditols and/or glycols from a mixed C5/C6 sugar stream without needlessly driving total recovery of the individual target alditols and/or glycols. The result is a highly efficient, low complexity process having enhanced production flexibility, reduced waste and greater overall yield than conventional processes directed to alditol or glycol production.

The present invention provides a catalyst composition comprising different metal oxides wherein the catalyst composition comprising Ce, Cr and Ni oxides and a process for preparation thereof. The catalyst composition is used for different reforming techniques for the production of syn gas (CO+H.sub.2) at the same time this material can be used in fuel cell as a anode for power generation as this synthesized material is having good thermal stability and can sustain various redox reaction cycles also.