A method 10 for processing hydrocarbons for recycling includes the steps of: a) heating solid and/or liquid hydrocarbons in a chamber 16 in the absence of air, to convert at least some of the hydrocarbons into hydrocarbon gas; b) reacting the hydrocarbon gas in a reactor 20 or conduit with a catalyst 22 including a transition metal or transition metal salt, and a carbide, to break the hydrocarbon gas down into hydrocarbon products; and c) collecting the hydrocarbon products or conveying the hydrocarbon products elsewhere for use.

A source material gas (31) is supplied to a catalyst (30), a first heating medium (21) is caused to flow through a first heat exchange section (22) so that a temperature of a surface of the first heat exchange section (22) on a catalyst side is maintained higher than a dew point of a reacted gas (32), a second heating medium (51) is caused to flow through a second heat exchange section (52) so that a temperature of a surface of the second heat exchange section (52) on a space (4) side is maintained not higher than the dew point of the reacted gas (32), and a liquid obtained by condensation in the space (4) is allowed to fall down so as to be separated from the source material gas.

An object of the present invention is to provide a new frameless catalytic thermal oxidation device capable of treating concentrations of harmful materials including NOx at a low temperature. Further, another object of the present invention is to provide a frameless catalytic thermal oxidation device capable of minimizing the occurrence of THC and minimizing a risk of accidents and environmental pollution which may occur in maintenance operations. According to the objects, the present invention provides a cartridge-type thermal oxidation device capable of being separated for maintenance, wherein a cartridge internal structure is configured so that the time while the material to be treated stays in a zone with the catalyst is increased, and a member capable of dropping and collecting powder generated by thermal oxidation reaction is configured.

A device for measuring the internal temperature of a reforming tube including a first structure having an axial part of tubular shape positioned in the lengthwise direction of a reforming tube and a radial part projecting radially towards the central axis of the reforming tube, a second structure of oblong shape having at least one thermocouple made of welded Nicrosil/Nisil conductors arranged longitudinally against the axial part and radially against the radial part, and an outer sheath enveloping the first structure and the second structure.

The present application discloses a supported PtZn intermetallic alloy catalyst, a method for preparing the same and application thereof. The catalyst uses SiO.sub.2 as a support and Zn as a promoter, and a small amount of active component Pt is supported; the weight percentage of Pt is 0.025%-1%, and the weight percentage of Zn is 0.025%-1.7%, a co-impregnation method is adopted in preparation, the SiO.sub.2 support is impregnated in aqueous solution of chloroplatinic acid and zinc nitrate, and then drying and high-temperature reduction are performed to obtain a PtZn/SiO.sub.2 catalyst. The catalyst has the advantages of high activity, high stability, low price and low toxicity. The catalyst provided by the present application is applicable to preparation of alkene through short-chain alkane dehydrogenation, in particular to preparation of propylene through propane dehydrogenation in a hydrogen atmosphere. Under high-temperature conditions, the dehydrogenation activity is very high, the propylene selectivity can reach more than 90%, the stability is good, and the amount of used Pt is small, the utilization rate is high, and it is cheaper than industrial Pt series catalysts.

The invention relates to a process, unit and reaction system of low-carbon alkane dehydrogenation, which comprises the following steps: C3-C5 low-carbon alkane feed gas, together with CO and/or CO.sub.2 process gas, get into reactor after being preheated to 200-500° C., contact with a Cr—Ce—Cl/Al.sub.2O.sub.3 dehydrogenation catalyst, a Cu—Ce—Ca—Cl/Al.sub.2O.sub.3 thermal generating agent and thermal storage/support inert alumina balls, and convert to dehydrogenation products for 5-30 minutes under the conditions: temperature, 500-700° C., pressure, 10-100 kPa and weight hourly space velocity (WHSV), 0.1-5 hours.sup.−1. The products formed enter the downstream separation unit for separating out the low-carbon alkenes. The periodic regeneration process of the catalyst bed includes steam purging, hot air regenerating, bed heating, evacuating and reducing at 560 to 730° C. and 0.01 to 1 MPa. Each cycle needs about 10-70 minutes. With such dehydrogenation process, the reaction heat balance is moderated, and temperature gradient and reaction severity in the catalyst bed are reduced. As a consequence, the catalytic conversion, product selectivity, operation cycle and service life are improved. The system energy consumption is reduced.

This disclosure relates to reactor systems and methods of decomposing ammonia. In some aspects, a catalyst reactor includes an elongated conduit extending along a longitudinal axis. The elongated conduit can include a wall defining an interior cavity, an inlet configured for receiving a first fluid, and an outlet to flow the first fluid out of the elongated conduit, the wall having an interior cross-section defined by a major axis, W, and a minor axis, H, the major axis and the minor axis defining an aspect ratio, α=W/H, wherein the aspect ratio is greater than 2.0; and a catalytic structure disposed within the interior cavity of the elongated conduit.

An apparatus for the production of hydrogen from a fuel source includes a combustor configured to receive a combustor fuel and convert the combustor fuel into a combustor heat; a reformer disposed annularly about the combustor, a removable structured catalyst support disposed within the gap and coated with a catalyst to induce combustor fuel combustion reactions that convert the combustor fuel to the combustor heat, and a combustor fuel injection aperture configured for mixing combustion fuel into the combustion catalyst. The combustor fuel injection aperture being disposed along a length of the combustion zone. The reformer and the combustor define a gap therebetween and the reformer is configured to receive the combustor heat.

The present disclosure relates to a device for accurately measuring photocatalytic efficiency. Additional embodiments of the present disclosure further relate to a method of utilizing the disclosed device, for example, to obtain accurate measurements of photocatalytic efficiency and a photocatalyst compatible with the device in the present disclosure. Application of the present disclosure may include the quantification of photocatalytic light conversion metrics such as in a research environment.

The invention is directed to a process for the purification of a raw hydrogen gas stream comprising hydrogen gas in an amount of 85-99%, said process comprising the step of contacting said raw hydrogen gas stream with an oxidized bed comprising an oxidized metal resulting in a waste gas stream comprising water and less than 5% hydrogen gas, and in a reduction of said oxidized metal; and a step of contacting a bed comprising a reduced metal with water to produce a purified hydrogen gas stream comprising more than 99% hydrogen gas, preferably comprising 99.97% or more hydrogen gas, and the oxidized metal. In a further aspect, the invention is directed to an apparatus suitable to carry out said process.