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).

The present specification discloses a membrane reactor comprising a reaction region; a permeate region; and a composite membrane disposed at a boundary of the reaction region and the permeate region, wherein the reaction region comprises a bed filled with a catalyst for dehydrogenation reaction, wherein the composite membrane comprises a support layer including a metal with a body-centered-cubic (BCC) crystal structure, and a catalyst layer including a palladium (Pd) or a palladium alloy formed onto the support layer, wherein ammonia (NH.sub.3) is supplied to the reaction region, the ammonia is converted into hydrogen (H.sub.2) by the dehydrogenation reaction in the presence of the catalyst for dehydrogenation reaction, and the hydrogen permeates the composite membrane and is emitted from the membrane reactor through the permeate region.

An engine includes a reformer, a reforming-air adjuster, a reforming-fuel supply unit, a reformed-gas adjuster, and a control unit. The reformer is configured to reform fuel into a reformed gas. When a start signal is input, the control unit controls the reforming-air adjuster and the reforming-fuel supply unit to a reformable state in which the fuel is reformable in the reformer, and the control unit controls the reformed-gas adjuster so that the reformed gas flows through the reformed-gas adjuster with a degree of opening smaller than a normal degree of opening that is a degree of opening of the reformed-gas adjuster when composition of the reformed gas is in a stable state before the composition of the reformed gas becomes in the stable state, for a given period of time including at least a period immediately after the engine starts.

Embodiments provide novel devices, nanowires, apparatuses, artificial leaves, photoelectrodes and membranes for photochemical energy production and methods of fabricating the same. The devices, apparatuses, artificial leaves, photoelectrodes, and membranes are planar and are embedded with nanowires, including InGaN nanowires. The unique devices, artificial leaves, apparatuses photoelectrodes, and nanowire-embedded membranes provide a high degree of flexibility and incorporate a large amount of indium, making them valuable for use for hydrogen production from sunlight and water. Embodiments also provide flexible substrates combining water oxidation and hydrogen reduction in a seamless manner to enhance the overall efficiency of water splitting.

Process for cracking hydrocarbon gases, wherein the hydrocarbon gas is passed through a flow channel of an absorptive receiver reactor (1, 30, 40), characterized in that cracking takes place during the passing through the receiver reactor (1, 30, 40), wherein in a first region (21) of the flow channel (2) the hydrocarbon gas is heated to its cracking temperature, in an adjoining second, downstream flow region (22) is heated to beyond its cracking temperature and in a third, further downstream region (23) of the flow channel is heated yet further and is brought therein into physical contact, over the cross-section of said region, with a reaction accelerator, after which the stream of products downstream of the reaction accelerator is discharged from the receiver reactor (1, 30, 40), and wherein the heating of the hydrocarbon gas to above its cracking temperature is achieved by absorption of blackbody radiation (20) which is given off by the reaction accelerator heated by solar radiation (7) incident thereupon to the hydrocarbon gas flowing towards it, in such a way that the hydrocarbon gas in the flow channel (2) and extending up to the reaction accelerator forms disc-shaped, consecutive temperature zones (60 to 67) of ever-increasing temperature extending transversely to the flow channel (2).

A system and a method for producing hydrogen and electrical power from an aqueous ammonia solution are provided. An exemplary system includes a distillation unit to produce ammonia gas from the aqueous ammonia solution, a compression unit to boost the pressure of the ammonia gas, a membrane separator to catalytically convert the ammonia gas to nitrogen and hydrogen and remove the hydrogen as a permeate, and a micro turbine to combust a retentate to generate energy.

In an apparatus producing hydrogen gas by the decomposition reaction of water using photocatalyst, its miniaturization is achieved while suppressing the decrease of production efficiency of hydrogen gas as low as possible or improving the efficiency. The apparatus 1 comprises a container portion 2 receiving water W; a photocatalyst member 3 immersed in the water, having photocatalyst which generates excited electrons and positive holes when irradiated with light, causes a decomposition reaction of the water and generates hydrogen gas; a light source 4 emitting the light irradiated to the photocatalyst member; and a heat exchange device 7 conducting waste heat of the light source to the water in the container portion; wherein the water to be decomposed on the photocatalyst member in the container portion is warmed by the waste heat of the light source by the heat exchange device.

The present disclosure relates to a dissimilar metal-doped cerium oxide including cerium oxide and a dissimilar metal other than the cerium oxide, in which a relationship of the following formula (1) is satisfied:

0.8≤|(D90)−(D10)|/D50≤2.0  (1) (in the formula (1), D10, D50, and D90 respectively represent the following: D10: particle diameter at which cumulative volume fraction is 10% D50: particle diameter at which cumulative volume fraction is 50% D90: particle diameter at which cumulative volume fraction is 90%).

The present disclosure relates to a multi-sandwich composite catalyst and a preparation method and application thereof. The present disclosure provides a preparation method of a multi-sandwich composite catalyst, comprises the following steps: sequentially depositing a first layer oxide, a first active metal, an oxide interlayer, a second active metal and a surface oxide on a template, and sequentially performing calcination and reduction, thereby obtaining a multi-sandwich composite catalyst; wherein the first active metal and the second active metal are different kinds of active metals. In the present disclosure, a multi-sandwich structure is formed by depositing the oxides and active metals alternately, so that the position and spacing distance of the active centers can be precisely controlled. The multi-sandwich composite catalyst prepared by the method provided described herein has a higher conversion than that of a catalyst without an interlayer when used for the catalytic reaction.

The present disclosure relates to a multi-sandwich composite catalyst and a preparation method and application thereof. The present disclosure provides a preparation method of a multi-sandwich composite catalyst, comprises the following steps: sequentially depositing a first layer oxide, a first active metal, an oxide interlayer, a second active metal and a surface oxide on a template, and sequentially performing calcination and reduction, thereby obtaining a multi-sandwich composite catalyst; wherein the first active metal and the second active metal are different kinds of active metals. In the present disclosure, a multi-sandwich structure is formed by depositing the oxides and active metals alternately, so that the position and spacing distance of the active centers can be precisely controlled. The multi-sandwich composite catalyst prepared by the method provided described herein has a higher conversion than that of a catalyst without an interlayer when used for the catalytic reaction.