A butadiene production system and a butadiene production method are provided in which butadiene can be produced with a high yield. The butadiene production system (1) includes: a gas preparation device (10) that heats raw materials to prepare a mixed gas including hydrogen and carbon monoxide; an ethanol production device (12) that is provided downstream of the gas preparation device (10) and brings the mixed gas including hydrogen and carbon monoxide into contact with a first catalyst to obtain ethanol; a butadiene production device (16) that is provided downstream of the ethanol production device (12) and brings the ethanol into contact with a second catalyst to obtain butadiene; and return means (18) for returning hydrogen, which is produced as a by-product in the butadiene production device (16), to the ethanol production device (12). In addition, in the butadiene production method, the butadiene production system (1) is used.

The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 2 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing a regeneration loop for the inert gas and at least one regeneration loop for the gas streams comprising oxygen.

The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 2 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing a regeneration loop for the inert gas and at least one regeneration loop for the gas streams comprising oxygen.

The present invention provides an electrocatalytic material and a method for making an electrocatalytic material. There is also provided an electrocatalytic material comprising amorphous metal or mixed metal oxides. There is also provided methods of forming an electrocatalyst, comprising an amorphous metal oxide film.

The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 4 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing three regeneration loops.

The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 4 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing three regeneration loops.

In this fuel cell electrode catalyst layer, a catalyst is supported on a carrier comprising inorganic oxide particles. The fuel cell electrode catalyst layer is provided with a porous structure. When a mercury penetration method is used to measure the pore size distribution of the porous structure, a peak is observed in the range spanning from 0.005 μm to 0.1 μm inclusive, and a peak is also observed in the range spanning from over 0.1 μm to not more than 1 μm. When P1 represents the peak intensity in the range spanning from 0.005 μm to 0.1 μm inclusive, and P2 represents the peak intensity in the range spanning from over 0.1 μm to not more than 1 μm, the value of P2/P1 is 0.2-10 inclusive. It is preferable that the inorganic oxide be tin oxide.

Novel transition element-embedded carbon materials and methods for forming the same. The embedded transition elements can be oxides or hydroxides and may include a transition metal. In some cases the transition element-embedded materials are catalytic material suitable for use in a variety of catalytic systems. According to one specific example, the transition element that is embedded is a niobia species.

Novel transition element-embedded carbon materials and methods for forming the same. The embedded transition elements can be oxides or hydroxides and may include a transition metal. In some cases the transition element-embedded materials are catalytic material suitable for use in a variety of catalytic systems. According to one specific example, the transition element that is embedded is a niobia species.

Provided is an oxygen reduction catalyst having a high oxygen reduction performance. An oxygen reduction catalyst according to the present embodiment includes a transition metal oxide to which an oxygen defect is introduced, and a layer that is provided on the transition metal oxide and that contains an electron conductive substance. A method for producing an oxygen reduction catalyst according to the present embodiment includes heating a transition metal carbonitride as a starting material in an oxygen-containing mixed gas. In addition, a method for producing an oxygen reduction catalyst according to the present embodiment includes heating a transition-metal phthalocyanine and a carbon fiber powder as starting materials in an oxygen-containing mixed gas.