Patent classifications
C07C29/159
Method and apparatus for selective alcohol upgrading
Methods for utilizing carbon dioxide to produce multi-carbon products are disclosed. The systems and methods of the present disclosure involve: reducing CO.sub.2 to produce a first product mixture comprising an alcohol product mixture comprising one or more alcohols and a paraffin product mixture comprising one or more paraffins; dehydrating the alcohol product mixture to form an olefin product mixture comprising one or more olefins; oligomerizing the olefin product mixture to form a higher olefin product mixture comprising unsaturated paraffins and optionally aromatics; and reducing the higher olefin product mixture to form a higher hydrocarbon product mixture comprising unsaturated paraffins and optionally aromatics. Catalyst materials and reaction conditions for individual steps are disclosed to optimize yield for ethanol or jet fuel range hydrocarbons.
Method and apparatus for selective alcohol upgrading
Methods for utilizing carbon dioxide to produce multi-carbon products are disclosed. The systems and methods of the present disclosure involve: reducing CO.sub.2 to produce a first product mixture comprising an alcohol product mixture comprising one or more alcohols and a paraffin product mixture comprising one or more paraffins; dehydrating the alcohol product mixture to form an olefin product mixture comprising one or more olefins; oligomerizing the olefin product mixture to form a higher olefin product mixture comprising unsaturated paraffins and optionally aromatics; and reducing the higher olefin product mixture to form a higher hydrocarbon product mixture comprising unsaturated paraffins and optionally aromatics. Catalyst materials and reaction conditions for individual steps are disclosed to optimize yield for ethanol or jet fuel range hydrocarbons.
PHOTOCATALYTIC CONVERSION OF CARBON DIOXIDE AND WATER INTO HYDROCARBONS
The present invention relates to photocatalytic materials for use in the conversion of CO.sub.2 to non-CO.sub.2 carbon containing products. The photocatalytic materials comprise a metal nanofiber and a carbon-based nanostructure bound to the surface of the metal nanofiber. Methods for preparing such materials are described, as well as their use in the conversion of CO.sub.2 to non-CO.sub.2 carbon containing products. For example, the photocatalytic materials of the invention may be used to convert CO.sub.2 to methanol and/or ethanol with high conversion rates.
PHOTOCATALYTIC CONVERSION OF CARBON DIOXIDE AND WATER INTO HYDROCARBONS
The present invention relates to photocatalytic materials for use in the conversion of CO.sub.2 to non-CO.sub.2 carbon containing products. The photocatalytic materials comprise a metal nanofiber and a carbon-based nanostructure bound to the surface of the metal nanofiber. Methods for preparing such materials are described, as well as their use in the conversion of CO.sub.2 to non-CO.sub.2 carbon containing products. For example, the photocatalytic materials of the invention may be used to convert CO.sub.2 to methanol and/or ethanol with high conversion rates.
HAFNIUM-BASED METAL-ORGANIC FRAMEWORKS AS EPOXIDE RING-OPENING CATALYSTS
Metal-organic frameworks (MOFs) having inorganic nodes that comprise an octahedral Hf.sub.6 cluster capped by eight .sub.3-ligands and having twelve octahedral edges, wherein the .sub.3-ligands are hydroxo ligands, oxo ligands or aquo ligands; and organic linkers connecting the organic nodes, the organic linkers comprising 1,3,6,8-tetrakis(p-benzoic acid)pyrene units; wherein eight of the twelve octahedral edges of the inorganic nodes are connected to the 1,3,6,8-tetrakis(p-benzoic acid)pyrene units are provided.
HAFNIUM-BASED METAL-ORGANIC FRAMEWORKS AS EPOXIDE RING-OPENING CATALYSTS
Metal-organic frameworks (MOFs) having inorganic nodes that comprise an octahedral Hf.sub.6 cluster capped by eight .sub.3-ligands and having twelve octahedral edges, wherein the .sub.3-ligands are hydroxo ligands, oxo ligands or aquo ligands; and organic linkers connecting the organic nodes, the organic linkers comprising 1,3,6,8-tetrakis(p-benzoic acid)pyrene units; wherein eight of the twelve octahedral edges of the inorganic nodes are connected to the 1,3,6,8-tetrakis(p-benzoic acid)pyrene units are provided.
HAFNIUM-BASED METAL-ORGANIC FRAMEWORKS AS EPOXIDE RING-OPENING CATALYSTS
Metal-organic frameworks (MOFs) having inorganic nodes that comprise an octahedral Hf.sub.6 cluster capped by eight .sub.3-ligands and having twelve octahedral edges, wherein the .sub.3-ligands are hydroxo ligands, oxo ligands or aquo ligands; and organic linkers connecting the organic nodes, the organic linkers comprising 1,3,6,8-tetrakis(p-benzoic acid)pyrene units; wherein eight of the twelve octahedral edges of the inorganic nodes are connected to the 1,3,6,8-tetrakis(p-benzoic acid)pyrene units are provided.
Zirconium- and hafnium-based metal-organic frameworks as epoxide ring-opening catalysts
Metal-organic frameworks (MOFs) and method of using the MOFs to catalyze reactions involving epoxide ring-opening mechanisms are provided. The structure of the MOFs can be represented by the formula: M.sub.6(.sub.3-ligand).sub.8(OH.sub.x).sub.8(TBAPy).sub.2, where M is Zr or Hf, the ligands are selected from hydroxo-, oxo- and aquo-ligands, and x is independently selected from 1 or 2.
Zirconium- and hafnium-based metal-organic frameworks as epoxide ring-opening catalysts
Metal-organic frameworks (MOFs) and method of using the MOFs to catalyze reactions involving epoxide ring-opening mechanisms are provided. The structure of the MOFs can be represented by the formula: M.sub.6(.sub.3-ligand).sub.8(OH.sub.x).sub.8(TBAPy).sub.2, where M is Zr or Hf, the ligands are selected from hydroxo-, oxo- and aquo-ligands, and x is independently selected from 1 or 2.
Zirconium- and hafnium-based metal-organic frameworks as epoxide ring-opening catalysts
Metal-organic frameworks (MOFs) and method of using the MOFs to catalyze reactions involving epoxide ring-opening mechanisms are provided. The structure of the MOFs can be represented by the formula: M.sub.6(.sub.3-ligand).sub.8(OH.sub.x).sub.8(TBAPy).sub.2, where M is Zr or Hf, the ligands are selected from hydroxo-, oxo- and aquo-ligands, and x is independently selected from 1 or 2.