The present invention discloses a process for the conversion of phenolics into aromatic hydrocarbons. In more detail, the present invention refers to a process for the selective hydrodeoxygenation of phenolic feeds into aromatic hydrocarbons, such as benzene, toluene, alkylbenzenes and others. The selective catalytic hydrodeoxygenation is performed in absence of external supply of molecular hydrogen.

The present invention discloses a process for the conversion of phenolics into aromatic hydrocarbons. In more detail, the present invention refers to a process for the selective hydrodeoxygenation of phenolic feeds into aromatic hydrocarbons, such as benzene, toluene, alkylbenzenes and others. The selective catalytic hydrodeoxygenation is performed in absence of external supply of molecular hydrogen.

A method of desulfurizing a sulfur-containing hydrocarbon feedstock includes introducing the sulfur-containing hydrocarbon feedstock within a reactor in the presence of a gas atmosphere and a catalyst structure, where the catalyst structure comprises a zeolite porous support structure including gallium (Ga) and molybdenum (Mo) loaded in the zeolite porous support structure. The gas atmosphere can include methane. At least 50% of sulfur content can be removed from the feedstock as a result of the desulfurizing method.

A process is disclosed for polishing a relatively highly pure stream of aromatic material bound for use as a petrochemical feedstock wherein the stream includes olefins and especially concerning, diolefins. The process comprises hydrotreating the highly pure aromatic stream with an unsulfided cobalt molybdenum catalyst that has low saturating activity for the aromatic but is active for saturating olefins and diolefins.

A process is disclosed for polishing a relatively highly pure stream of aromatic material bound for use as a petrochemical feedstock wherein the stream includes olefins and especially concerning, diolefins. The process comprises hydrotreating the highly pure aromatic stream with an unsulfided cobalt molybdenum catalyst that has low saturating activity for the aromatic but is active for saturating olefins and diolefins.

The application describes a process where methane or any short chained hydrocarbon could be catalytically coupled with an oxygenate (preferably derived from thermal processing of biomass) to dehydrate and produce a deoxygenated hydrocarbon. The presence of oxygen in biomass derivatives adversely affects its ability to be further processed into hydrocarbon fuels because the resulting water poisons many catalysts (including alumina containing catalysts, zeolites, etc.) found in petrochemical refineries. While commonly used hydrodeoxygenation methods require expensive hydrogen to instigate deoxygenation, the present process uses short chained hydrocarbons (such as methane or natural gas) to instigate hydrodeoxygenation.

The application describes a process where methane or any short chained hydrocarbon could be catalytically coupled with an oxygenate (preferably derived from thermal processing of biomass) to dehydrate and produce a deoxygenated hydrocarbon. The presence of oxygen in biomass derivatives adversely affects its ability to be further processed into hydrocarbon fuels because the resulting water poisons many catalysts (including alumina containing catalysts, zeolites, etc.) found in petrochemical refineries. While commonly used hydrodeoxygenation methods require expensive hydrogen to instigate deoxygenation, the present process uses short chained hydrocarbons (such as methane or natural gas) to instigate hydrodeoxygenation.