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contributor authorChristian Wieckert
contributor authorAldo Steinfeld
date accessioned2017-05-09T00:08:40Z
date available2017-05-09T00:08:40Z
date copyrightFebruary, 2002
date issued2002
identifier issn0199-6231
identifier otherJSEEDO-28314#55_1.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/127458
description abstractThe solar thermal reduction of ZnO, using solar process heat and CH4 or C as reducing agent, is investigated for CH4:ZnO or C:ZnO molar ratios ranging from 0 (thermal decomposition at above about 2000°C) to 1 (stoichiometric reduction at above about 1000°C). At 1400°C, in thermodynamic equilibrium ZnO can be completely reduced using a CH4:ZnO molar ratio of 0.3 and produces one fuel (Zn-metal) rather than two for the stoichiometric case (Zn and syngas). The maximal reactor thermal efficiency without heat recovery from the offgas, defined as the ratio of the heating-value of the zinc produced to the total thermal energy input, is 55%. CO2-emissions are reduced by a factor of 10–15 compared to fossil-fuel-based zinc-production technologies. For a closed materials cycle, in which power is extracted from the solar zinc using a fuel cell and the ZnO formed is recycled to the solar reactor, the total exergy efficiency, defined as the work output of the fuel cell to the thermal energy input, varies between 30 to 40% when based on the absorbed solar power in the reactor. These efficiency values are very encouraging, especially since the solar ZnO/Zn cycle allows—in contrast to other regenerative power plants—to store and transport solar energy.
publisherThe American Society of Mechanical Engineers (ASME)
titleSolar Thermal Reduction of ZnO Using CH4:ZnO and C:ZnO Molar Ratios Less Than 1
typeJournal Paper
journal volume124
journal issue1
journal titleJournal of Solar Energy Engineering
identifier doi10.1115/1.1434980
journal fristpage55
journal lastpage62
identifier eissn1528-8986
keywordsSolar energy
keywordsEquilibrium (Physics)
keywordsTemperature
keywordsFuels AND Methane
treeJournal of Solar Energy Engineering:;2002:;volume( 124 ):;issue: 001
contenttypeFulltext


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