Accurately computing solar irradiance on external facades is a prerequisite for reliably predicting thermal behavior and cooling loads of buildings. Validation of radiation models and algorithms implemented in building energy simulation codes is an essential endeavor for evaluating solar gain models. Seven solar radiation models implemented in four building energy simulation codes were investigated: (1) isotropic sky, (2) Klucher, (3) Hay-Davies, (4) Reindl, (5) Muneer, (6) 1987 Perez, and (7) 1990 Perez models. The building energy simulation codes included: EnergyPlus, DOE-2.1E, TRNSYS-TUD, and ESP-r. Solar radiation data from two 25 days periods in October and March/April, which included diverse atmospheric conditions and solar altitudes, measured on the EMPA campus in a suburban area in Duebendorf, Switzerland, were used for validation purposes. Two of the three measured components of solar irradiances - global horizontal, diffuse horizontal and direct-normal - were used as inputs for calculating global irradiance on a south-west façade. Numerous statistical parameters were employed to analyze hourly measured and predicted global vertical irradiances. Mean absolute differences for both periods were found to be: (1) 13.7% and 14.9% for the isotropic sky model, (2) 9.1% for the Hay-Davies model, (3) 9.4% for the Reindl model, (4) 7.6% for the Muneer model, (5) 13.2% for the Klucher model, (6) 9.0%, 7.7%, 6.6%, and 7.1% for the 1990 Perez models, and (7) 7.9% for the 1987 Perez model. Detailed sensitivity analyses using Monte Carlo and fitted effects for N-way factorial analyses were applied to assess how uncertainties in input parameters propagated through one of the building energy simulation codes and impacted the output parameter. The implications of deviations in computed solar irradiances on predicted thermal behavior and cooling load of buildings are discussed
Two-step thermochemical cycles for splitting CO 2 with Zn/ZnO and FeO/Fe 3 O 4 redox pairs using concentrated solar energy are considered. Thermogravimetric-based kinetic analyses were performed for the reduction of CO 2 to CO with Zn and FeO. Both reactions are characterized by an initial fast interface-controlled regime followed by a slow diffusion-controlled regime, which are described using a shell-core kinetic model. In the interface-controlled regime, a power rate law is applied with apparent activation energies 113.7 and 73.4 kJ mol -1 , and corresponding reaction orders 0.339 and 0.792, for the Zn/CO 2 and FeO/CO 2 systems, respectively. In the diffusion-controlled regime, limited by the ion mobility through the oxide shells, the apparent activation energies are 162.3 kJ mol -1 for Zn/CO 2 and 106.4 kJ mol -1 for FeO/CO 2 . Additional reaction mechanisms above the Zn melting point for Zn/CO 2 reactions are postulated.
Two-step thermochemical cycles for CO 2 reduction via Zn/ZnO and FeO/Fe 3 O 4 redox reactions are considered. The first, endothermic step is the thermal dissociation of the metal oxide into the metal or a reduced valence metal oxide and O 2 using concentrated solar energy as the source of high-temperature process heat. The second, nonsolar, exothermic step is the reaction of the reduced metal/metal oxide with CO 2 , yielding CO and/or C, together with the initial form of the metal oxide that is recycled to the first step. Chemical equilibrium compositions of the pertinent reactions are computed as a function of temperature and pressure. A second-law thermodynamic analysis for the net reaction of CO 2 ) CO + 0.5O 2 indicates a maximal solar-chemical energy conversion efficiency of 39 and 29% for the Zn/ZnO and FeO/Fe 3 O 4 cycle, respectively. Efficiencies are lower for both cycles yielding C. Major sources of irreversibility are associated with the re-radiation losses of the solar reactor operating at 2000 K and the quenching of its products to avoid recombination.
This article provides a comprehensive overview of the work to date on the two‑step solar H2O and/or CO2 splitting thermochemical cycles with Zn/ZnO redox reactions to produce H2 and/or CO, i.e., synthesis gas—the precursor to renewable liquid hydrocarbon fuels. The two-step cycle encompasses: (1) The endothermic dissociation of ZnO to Zn and O2 using concentrated solar energy as the source for high-temperature process heat; and (2) the non-solar exothermic oxidation of Zn with H2O/CO2 to generate H2/CO, respectively; the resulting ZnO is then recycled to the first step. An outline of the underlying science and the technological advances in solar reactor engineering is provided along with life cycle and economic analyses.
The solar production of syngas from H2O and CO2 is examined via two-step thermochemical cycles based on Zn/ZnO and FeO/Fe3O4 redox reactions. The first, endothermic step is the thermal dissociation of the metal oxide using concentrated solar radiation as the energy source of high-temperature process heat. The second, nonsolar, exothermic step is the reaction of the metal or reduced metal oxide with a mixture of H2O and CO2 yielding syngas (H2 and CO), together with the initial form of the metal oxide that is recycled to the first step. Chemical equilibrium compositions for the systems of Zn and FeO with CO2 + H2O were computed as a function of temperature and pressure for different stoichiometries. A series of dynamic thermogravimetric experimental runs in the range 673−1423 K was carried out to evaluate the reaction kinetics and syngas quality of the second step. The molar flow rate fractions of the gaseous products exhibited linear dependencies on the molar flow rate fractions of the gaseous reactants for both the FeO/Fe3O4 and Zn/ZnO systems.
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