Patent classifications
B01J21/18
PLANT LEAVES-DERIVED CARBON MATERIAL DOPED WITH TWO METALS AND PREPARATION AND USE THEREOF
A plant leaves-derived carbon material doped with two metals and preparation and use thereof are provided, the carbon material prepared by carbonizing, in an inert atmosphere, plant leaves which have absorbed ions of two metals M1 and M2. The metal M1 is Co, Mn, or Fe. The metal M2 is Ni, Cu, or Zn. The carbon material can be used as an efficient, green, and safe catalyst for the selective oxidation of cycloalkanes to produce cycloalkanols and cycloalkanones, and enable an increased selectivity of the target products (thus less by-products), a low yield of cycloalkyl peroxides, reduced reaction temperature, low environmental impact, and safe production.
PLANT LEAVES-DERIVED CARBON MATERIAL DOPED WITH TWO METALS AND PREPARATION AND USE THEREOF
A plant leaves-derived carbon material doped with two metals and preparation and use thereof are provided, the carbon material prepared by carbonizing, in an inert atmosphere, plant leaves which have absorbed ions of two metals M1 and M2. The metal M1 is Co, Mn, or Fe. The metal M2 is Ni, Cu, or Zn. The carbon material can be used as an efficient, green, and safe catalyst for the selective oxidation of cycloalkanes to produce cycloalkanols and cycloalkanones, and enable an increased selectivity of the target products (thus less by-products), a low yield of cycloalkyl peroxides, reduced reaction temperature, low environmental impact, and safe production.
CATALYST LAYER, MEMBRANE ELECTRODE ASSEMBLY FOR SOLID POLYMER FUEL CELL, AND SOLID POLYMER FUEL CELL
A catalyst layer including: a catalyst-supported carbon including a catalyst including platinum supported on a carbon carrier; and an ionomer, in which the catalyst-supported carbon has a mesopore having a pore diameter of from 2 nm to less than 10 nm in a pore distribution obtained by a nitrogen adsorption method, at least a part of the ionomer exists in the mesopore having a pore diameter of from 2 nm to less than 10 nm, a content of the ionomer with respect to 100 parts by mass of the carbon carrier is 100 parts by mass or more, and an occupancy rate of the ionomer in a total volume of the mesopore having a pore diameter of from 2 nm to less than 10 nm is 50% by volume or less.
AMMONIA DECOMPOSITION CATALYST AND METHOD OF DECOMPOSING AMMONIA USING THE CATALYST
Provided are an ammonia decomposition catalyst and a method of decomposing ammonia. The ammonia decomposition catalyst includes an activated carbon carrier and a metal loaded on the carrier, wherein a Brunauer, Emmett and Teller (BET) specific surface area of the carrier is about 850 m.sup.2/g or more, and the metal includes cerium (Ce).
AMMONIA DECOMPOSITION CATALYST AND METHOD OF DECOMPOSING AMMONIA USING THE CATALYST
Provided are an ammonia decomposition catalyst and a method of decomposing ammonia. The ammonia decomposition catalyst includes an activated carbon carrier and a metal loaded on the carrier, wherein a Brunauer, Emmett and Teller (BET) specific surface area of the carrier is about 850 m.sup.2/g or more, and the metal includes cerium (Ce).
SYNTHESIS OF ATOMICALLY DISPERSED M-N-C CATALYSTS VIA SELECTIVE METALATION
A method of making an M-N—C catalyst is disclosed. The method includes the steps of (a) contacting an N-doped carbon support with a basic solution that includes a metal salt, whereby the N-doped carbon support is metalated by the metal cation of the metal salt to form one or more chelated metal-nitrogen complexes (MN.sub.x species); and (b) subsequently contacting the metalated N-doped carbon support with an acid, whereby the one or more MN.sub.x species formed on the N-doped carbon support in step (a) remain intact while other species are removed. The resulting composition may be catalytically activated by heat treating the composition. The activated catalyst may be used to catalyze a wide range of chemical reactions.
SYNTHESIS OF ATOMICALLY DISPERSED M-N-C CATALYSTS VIA SELECTIVE METALATION
A method of making an M-N—C catalyst is disclosed. The method includes the steps of (a) contacting an N-doped carbon support with a basic solution that includes a metal salt, whereby the N-doped carbon support is metalated by the metal cation of the metal salt to form one or more chelated metal-nitrogen complexes (MN.sub.x species); and (b) subsequently contacting the metalated N-doped carbon support with an acid, whereby the one or more MN.sub.x species formed on the N-doped carbon support in step (a) remain intact while other species are removed. The resulting composition may be catalytically activated by heat treating the composition. The activated catalyst may be used to catalyze a wide range of chemical reactions.
HIGH-CARBON BIOGENIC REAGENTS AND USES THEREOF
This invention provides processes and systems for converting biomass into high-carbon biogenic reagents that are suitable for a variety of commercial applications. Some embodiments employ pyrolysis in the presence of an inert gas to generate hot pyrolyzed solids, condensable vapors, and non-condensable gases, followed by separation of vapors and gases, and cooling of the hot pyrolyzed solids in the presence of the inert gas. Additives may be introduced during processing or combined with the reagent, or both. The biogenic reagent may include at least 70 wt%, 80 wt%, 90 wt%, 95 wt%, or more total carbon on a dry basis. The biogenic reagent may have an energy content of at least 12,000 Btu/lb, 13,000 Btu/lb, 14,000 Btu/lb, or 14,500 Btu/lb on a dry basis. The biogenic reagent may be formed into fine powders, or structural objects. The structural objects may have a structure and/or strength that derive from the feedstock, heat rate, and additives.
HIGH-CARBON BIOGENIC REAGENTS AND USES THEREOF
This invention provides processes and systems for converting biomass into high-carbon biogenic reagents that are suitable for a variety of commercial applications. Some embodiments employ pyrolysis in the presence of an inert gas to generate hot pyrolyzed solids, condensable vapors, and non-condensable gases, followed by separation of vapors and gases, and cooling of the hot pyrolyzed solids in the presence of the inert gas. Additives may be introduced during processing or combined with the reagent, or both. The biogenic reagent may include at least 70 wt%, 80 wt%, 90 wt%, 95 wt%, or more total carbon on a dry basis. The biogenic reagent may have an energy content of at least 12,000 Btu/lb, 13,000 Btu/lb, 14,000 Btu/lb, or 14,500 Btu/lb on a dry basis. The biogenic reagent may be formed into fine powders, or structural objects. The structural objects may have a structure and/or strength that derive from the feedstock, heat rate, and additives.
NITROGEN-CONTAINING CARBON MATERIAL AND METHOD FOR PRODUCING SAME
A nitrogen-containing carbon material includes carbon atoms, nitrogen atoms, and halogen atoms. The nitrogen-containing carbon material has a ratio of a number of moles of pyridinic nitrogen atoms to a total number of moles of the nitrogen atoms that is higher than 59% and a total content ratio of the nitrogen atoms with respect to the nitrogen-containing carbon material that is 7 at % or higher. The nitrogen-containing carbon material includes a fused polycyclic aromatic moiety formed by condensation of three or more aromatic rings, and the fused polycyclic aromatic moiety includes a partial structure for two pyridinic nitrogen atoms to be linked to each other through two carbon atoms.