Hydrogen production catalyst, production method of the same and hydrogen production method

摘要

The drive of direct-heat-supply type reforming of hydrocarbon at ordinary temperature is necessary in order to realize a self-sustaining, on-site reforming type fuel cell system which does not necessitate the supply of energy from the outside. According to the invention, an oxide, CeO2 or Pr6O11, or a Ce/Zr or Ce/Zr/Y double oxide is used as the oxide containing a rare earth element capable of changing the oxidation number with an active metal and oxygen defects are introduced into the oxide or double oxide by activating the oxide or double oxide with a reducing gas at high temperature. When a reaction gas containing hydrocarbon and oxygen is passed though the catalyst at low temperature, the oxygen defects react with oxygen and thereby return to the original oxide. Since this return reaction is an exothermic reaction, the catalyst itself is heated, which acts as the driving force for advancing the combustion of the hydrocarbon, whereby the catalyst layer is further heated and the reforming is advanced to from hydrogen. Thus, the hydrogen-producing reaction can be driven even at low temperature, particularly ordinary temperature.

主权项

1. A method for producing a catalyst for hydrogen of hydrocarbon,
wherein the catalyst is for reacting oxygen lattice defects introduced in a complex oxide with oxygen added in reaction gas containing hydrocarbon to generate heat, and to thereby heat the catalyst to a temperature for hydrogen reduction reaction of the hydrocarbon, and wherein a support for the catalyst is composed using a complex of Zr and Ce; and wherein the method comprises: a first step for calcining the support in an oxidizing atmosphere and at a prescribed temperature before or after loading Rh as an active metal to thereby obtain a complex oxide of Ce and Zr as a precursor, a second step for treating the precursor of complex oxide loading Rh in a reducing atmosphere at a prescribed temperature and for a prescribed amount of time to thereby introduce oxygen lattice defects into the complex oxide to activate the precursor, and to thereby produce an activated precursor in the form of Rh/CexZr1-xO2, wherein x is from 0.25 to 0.75, and a third step for retaining the activated precursor Rh/CexZr1-xO2 in an inert atmosphere.