Abstract:A solar-thermal aerosol flow reactor has been constructed, installed, and tested with the High-Flux Solar Furnace (HFSF) at the National Renewable Energy Laboratory (NREL). Experiments
were successfully carried out for the dissociation of methane to produce hydrogen and carbon
black and for the dry reforming of methane with carbon dioxide to form syngas (hydrogen and
carbon monoxide). Approximately 90% dissociation of methane was achieved in a 25-mm diameter
quartz reaction tube illuminated with a solar flux o… Show more
“…In order to achieve a net CO 2 conversion, the heat of reaction must not be created by burning fossil fuels. Instead solar-thermal reactors are an interesting development [24] and could be used in the future. Aside from environmental aspects, methane dry reforming is of general interest to the chemical industry because it delivers a lower H 2 =CO ratio than steam reforming which is desirable, e.g.…”
Methane activation by heterogeneous catalysis will play a key role to secure the supply of energy, chemicals and fuels in the future. Methane is the main constituent of natural gas and biogas and it is also found in crystalline hydrates at the continental slopes of many oceans and in permafrost areas. In view of this vast reserves and resources, the use of methane as chemical feedstock has to be intensified. The present review presents recent results and developments in heterogeneous catalytic methane conversion to synthesis gas, hydrogen cyanide, ethylene, methanol, formaldehyde, methyl chloride, methyl bromide and aromatics. After presenting recent estimates of methane reserves and resources the physico-chemical challenges of methane activation are discussed. Subsequent to this recent results in methane conversion to synthesis gas by steam reforming, dry reforming, autothermal reforming and catalytic partial oxidation are presented. The high temperature methane conversion to hydrogen cyanide via the BMA-process and the Andrussow-process is considered as well. The second part of this review focuses on one-step conversion of methane into chemicals. This includes the oxidative coupling of methane to ethylene mediated by oxygen and sulfur, the direct oxidation of methane to formaldehyde and methanol, the halogenation and oxyhalogenation of methane to methyl chloride and methyl bromide and finally the non-oxidative methane aromatization to benzene and related aromates. Opportunities and limits of the various activation strategies are discussed.
“…In order to achieve a net CO 2 conversion, the heat of reaction must not be created by burning fossil fuels. Instead solar-thermal reactors are an interesting development [24] and could be used in the future. Aside from environmental aspects, methane dry reforming is of general interest to the chemical industry because it delivers a lower H 2 =CO ratio than steam reforming which is desirable, e.g.…”
Methane activation by heterogeneous catalysis will play a key role to secure the supply of energy, chemicals and fuels in the future. Methane is the main constituent of natural gas and biogas and it is also found in crystalline hydrates at the continental slopes of many oceans and in permafrost areas. In view of this vast reserves and resources, the use of methane as chemical feedstock has to be intensified. The present review presents recent results and developments in heterogeneous catalytic methane conversion to synthesis gas, hydrogen cyanide, ethylene, methanol, formaldehyde, methyl chloride, methyl bromide and aromatics. After presenting recent estimates of methane reserves and resources the physico-chemical challenges of methane activation are discussed. Subsequent to this recent results in methane conversion to synthesis gas by steam reforming, dry reforming, autothermal reforming and catalytic partial oxidation are presented. The high temperature methane conversion to hydrogen cyanide via the BMA-process and the Andrussow-process is considered as well. The second part of this review focuses on one-step conversion of methane into chemicals. This includes the oxidative coupling of methane to ethylene mediated by oxygen and sulfur, the direct oxidation of methane to formaldehyde and methanol, the halogenation and oxyhalogenation of methane to methyl chloride and methyl bromide and finally the non-oxidative methane aromatization to benzene and related aromates. Opportunities and limits of the various activation strategies are discussed.
“…In the solar field, very high sunlight concentration factors (about 3000) are needed to reach temperatures over 1500 K [3,[22][23][24][25][26]. There are already some designs and experimental set-ups that could be useful for long-term generation of H 2 [27].…”
“…1, that was obtained from Gemini software [7] (software for thermodynamic equilibrium calculation developed by Thermodata), shows that methane decomposition is complete at about 1300 K. However, the reaction is not kinetically favorable [8,9], and a higher temperature is required to obtain high methane to hydrogen conversion rates and high-quality CB. Dahl et al [10] obtained exactly the same equilibrium products than that shown in Fig. 1, and they found that trace products at 1500 K include acetylene, ethylene, butylene, propylene, ethane at quantities less than 1 × 10 −3 moles for 1 mole of methane fed.…”
Section: Introductionmentioning
confidence: 55%
“…The reaction is kinetically hindered and the residence time (t r ) of the reactant in the high-temperature reacting zone (for a nozzle type b, i.e. 10 mm diameter and 10 mm cavity length, and a global flow rate of 1.1 L n / min, t r is about 40 ms at normal conditions and 8 ms at 1500 K, 1 atm) is not high enough to reach significant conversion [10]. Tables 2 and 3 list the results obtained with a 2 m-diameter concentrator and the corresponding operating conditions.…”
Section: Preliminary Experiments With a 15 M-diameter Solar Concentrmentioning
confidence: 99%
“…The indirect heating concept requires high-temperature material with drastic specifications, and the direct heating concept may lead to severe problems of optical window breakage due to possible carbon deposition. Tubular and vortex-type solar reactors have been tested by others [5,10,[14][15][16][17][18], they used either direct or indirect heating of the reactant by concentrated solar energy. In the experiment of Dahl et al [5,10,18], an Ar/CH 4 mixture is decomposed in an indirect solar heating reactor composed of concentric vertical graphite tubes.…”
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