Embodiments of the present disclosure describe a treated iron ore catalyst. Embodiments of the present disclosure further describe a method of preparing a treated iron ore catalyst comprising dehydrating an iron ore, milling the iron ore to a selected particle size, and reducing the iron ore to form a treated iron ore catalyst. Another embodiment of the present disclosure is a method of using a treated iron ore catalyst comprising contacting a feed gas with a treated iron ore catalyst to produce hydrogen and graphene.

A phenol alkylation catalyst exhibiting a desirable combination of activity, selectivity, and regenerability is prepared from a catalyst precursor that includes specific amounts of magnesium oxide, copper oxide or a copper oxide precursor, a hydrous magnesium aluminosilicate-containing binder, a pore-former, a lubricant, and water. Methods of forming and regenerating the catalyst, as well as a phenol alkylation method, are described.

A phenol alkylation catalyst exhibiting a desirable combination of activity, selectivity, and regenerability is prepared from a catalyst precursor that includes specific amounts of magnesium oxide, copper oxide or a copper oxide precursor, a hydrous magnesium aluminosilicate-containing binder, a pore-former, a lubricant, and water. Methods of forming and regenerating the catalyst, as well as a phenol alkylation method, are described.

The present invention relates to preparation of catalyst for production of olefinic hydrocarbons by dehydrogenation of their corresponding paraffins, particularly propylene from propane, comprising a metal oxide or combination of metal oxides utilizing spent catalyst from Fluid Catalytic Cracking (FCC)/Resid Fluid Catalytic Cracking (RFCC) processes. The metal oxides are possibly from transition metal group, particularly from groups VB, VIB, VIII, and Lanthanide series, and at least one metal from alkali group. The catalyst support used is spent catalyst or modified spent catalyst or combination thereof. The said catalyst can be used for both non-oxidative Propane Dehydrogenation (PDH) and Oxidative Propane Dehydrogenation (OPDH) process in the presence of CO.sub.2.

The present invention relates to preparation of catalyst for production of olefinic hydrocarbons by dehydrogenation of their corresponding paraffins, particularly propylene from propane, comprising a metal oxide or combination of metal oxides utilizing spent catalyst from Fluid Catalytic Cracking (FCC)/Resid Fluid Catalytic Cracking (RFCC) processes. The metal oxides are possibly from transition metal group, particularly from groups VB, VIB, VIII, and Lanthanide series, and at least one metal from alkali group. The catalyst support used is spent catalyst or modified spent catalyst or combination thereof. The said catalyst can be used for both non-oxidative Propane Dehydrogenation (PDH) and Oxidative Propane Dehydrogenation (OPDH) process in the presence of CO.sub.2.

The presently disclosed embodiments relate to the utilization of coal-derived fine mineral matter in chemical recycling of plastics or of solid mixed plastic waste. The instantly disclosed mineral based catalyst benefits the processes of catalytic cracking, gasification and steam reforming to maximize carbon utilization and production of plastics of original quality from recycled or renewable feedstocks while reducing the plastic pollution in the environment. The catalyst can be based on inorganic fine mineral matter, a natural ancient mineral mixture found in coal deposits and containing a plurality of transition metals, such as iron, copper, and manganese, as well as calcium, barium, magnesium, potassium, sodium, which can act as co-catalysts. Addition of the catalyst can convert plastic to syngas at a faction of the energy of conventional technologies.

A direct decomposition device for hydrocarbons for directly decomposing hydrocarbons into carbon and hydrogen includes a rector containing a catalyst including a plurality of metal particles with an iron purity of 86% or more. The reactor is configured to be supplied with a raw material gas containing hydrocarbons.

A direct decomposition device for hydrocarbons for directly decomposing hydrocarbons into carbon and hydrogen includes a rector containing a catalyst including a plurality of metal particles with an iron purity of 86% or more. The reactor is configured to be supplied with a raw material gas containing hydrocarbons.

A simple approach to produce mixed Cu/Cu.sub.2O nanocrystals having a specific morphology by controlling the reaction temperature during Cu/Cu.sub.2O nanocrystals synthesis. Other variables are kept constant, such as the amount of reactants, while the reaction temperatures is maintained at a predetermined temperature of 70 C., 30 C. or 0 C., which are used to produce different and controlled morphologies for the Cu/Cu.sub.2O nanocrystals. The reaction mixture includes a copper ion contributor, a capping agent, a pH adjustor, and reducing agent. The reaction mixture is held at the predetermined temperature for three hours to produce the Cu/Cu.sub.2O nanocrystals. The synthesis method has advantages such as mass production, easy operation, and high reproducibility.

A simple approach to produce mixed Cu/Cu.sub.2O nanocrystals having a specific morphology by controlling the reaction temperature during Cu/Cu.sub.2O nanocrystals synthesis. Other variables are kept constant, such as the amount of reactants, while the reaction temperatures is maintained at a predetermined temperature of 70 C., 30 C. or 0 C., which are used to produce different and controlled morphologies for the Cu/Cu.sub.2O nanocrystals. The reaction mixture includes a copper ion contributor, a capping agent, a pH adjustor, and reducing agent. The reaction mixture is held at the predetermined temperature for three hours to produce the Cu/Cu.sub.2O nanocrystals. The synthesis method has advantages such as mass production, easy operation, and high reproducibility.