María Erans
Cranfield University
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Publication
Featured researches published by María Erans.
Faraday Discussions | 2016
María Erans; Theodor Beisheim; Vasilije Manovic; M. Jeremiáš; Kumar Patchigolla; Heiko Dieter; Lunbo Duan; Edward J. Anthony
Four types of synthetic sorbents were developed for high-temperature post-combustion calcium looping CO2 capture using Longcal limestone. Pellets were prepared with: lime and cement (LC); lime and flour (LF); lime, cement and flour (LCF); and lime, cement and flour doped with seawater (LCFSW). Flour was used as a templating material. All samples underwent 20 cycles in a TGA under two different calcination conditions. Moreover, the prepared sorbents were tested for 10 carbonation/calcination cycles in a 68 mm-internal-diameter bubbling fluidized bed (BFB) in three environments: with no sulphur and no steam; in the presence of sulphur; and with steam. When compared to limestone, all the synthetic sorbents exhibited enhanced CO2 capture performance in the BFB experiments, with the exception of the sample doped with seawater. In the BFB tests, the addition of cement binder during the pelletisation process resulted in the increase of CO2 capture capacity from 0.08 g CO2 per g sorbent (LF) to 0.15 g CO2 per g sorbent (LCF) by the 10th cycle. The CO2 uptake in the presence of SO2 dramatically declined by the 10th cycle; for example, from 0.22 g CO2 per g sorbent to 0.05 g CO2 per g sorbent in the case of the untemplated material (LC). However, as expected all samples showed improved performance in the presence of steam, and the decay of reactivity during the cycles was less pronounced. Nevertheless, in the BFB environment, the templated pellets showed poorer CO2 capture performance. This is presumably because of material loss due to attrition under the FB conditions. By contrast, the templated materials performed better than untemplated materials under TGA conditions. This indicates that the reduction of attrition is critical when employing templated materials in realistic systems with FB reactors.
Journal of Visualized Experiments | 2017
María Erans; M. Jeremiáš; Vasilije Manovic; Edward J. Anthony
Calcium looping (CaL) is a post-combustion CO2 capture technology that is suitable for retrofitting existing power plants. The CaL process uses limestone as a cheap and readily available CO2 sorbent. While the technology has been widely studied, there are a few available options that could be applied to make it more economically viable. One of these is to increase the oxygen concentration in the calciner to reduce or eliminate the amount of recycled gas (CO2, H2O and impurities); therefore, decreasing or removing the energy necessary to heat the recycled gas stream. Moreover, there is a resulting increase in the energy input due to the change in the combustion intensity; this energy is used to enable the endothermic calcination reaction to occur in the absence of recycled flue gases. This paper presents the operation and first results of a CaL pilot plant with 100% oxygen combustion of natural gas in the calciner. The gas coming into the carbonator was a simulated flue gas from a coal-fired power plant or cement industry. Several limestone particle size distributions are also tested to further explore the effect of this parameter on the overall performance of this operating mode. The configuration of the reactor system, the operating procedures, and the results are described in detail in this paper. The reactor showed good hydrodynamic stability and stable CO2 capture, with capture efficiencies of up to 70% with a gas mixture simulating the flue gas of a coal-fired power plant.
Thermal Science | 2016
María Erans; Dawid P. Hanak; Jordi Mir; Edward J. Anthony; Vasilije Manovic
Calcium looping is promising for large-scale CO2 capture in the power generation and industrial sectors due to the cheap sorbent used and the relatively low energy penalties achieved with this process. Because of the high operating temperatures the heat utilisation is a major advantage of the process, since a significant amount of additional power can be generated from it. However, this increases its complexity and capital costs. Therefore, not only the energy efficiency performance is im- portant for these cycles, but also the capital costs must be taken into account, i. e. techno-economic analyses are required in order to determine which parameters and configurations are optimal to enhance technology viability in different integration scenarios. In this study the integration scenarios of calcium looping and natural gas combined cycles are explored. The process models of the natural gas combined cy- cles and calcium looping CO 2 capture plant are developed to explore the most promising scenarios for natural gas combined cycles-calcium looping integration with regard to efficiency penalties. Two scenarios are analysed in detail, and show that the system with heat recovery steam generator before and after the capture plant exhibited better performance of 49.1% efficiency compared with that of 45.7% when only one heat recovery steam generator is located after the capture plant. However, the techno-economic analyses showed that the more energy efficient case, with two heat recovery steam generators, implies relatively higher cost of electrici- ty, 44.1 €/MWh, when compared to that of the reference plant system (33.1 €/MWh). The predicted cost of CO 2 avoided for the case with two heat recovery steam gener- ators is 29.3 € per tonne of CO2.
Applied Energy | 2016
María Erans; Vasilije Manovic; Edward J. Anthony
Industrial & Engineering Chemistry Research | 2016
Lunbo Duan; Zhijian Yu; María Erans; Yingjie Li; Vasilije Manovic; Edward J. Anthony
Industrial & Engineering Chemistry Research | 2016
Lunbo Duan; Chenglin Su; María Erans; Yingjie Li; Edward J. Anthony; Huichao Chen
Fuel | 2017
María Erans; Francesca Cerciello; Antonio Coppola; Osvalda Senneca; Fabrizio Scala; Vasilije Manovic; Edward J. Anthony
Chemical Engineering Journal | 2018
Dawid P. Hanak; María Erans; Seyed Ali Nabavi; M. Jeremiáš; Luis M. Romeo; Vasilije Manovic
Journal of Energy Chemistry | 2017
Syed Kumail Haider; María Erans; Felix Donat; Lunbo Duan; Stuart A. Scott; Vasilije Manovic; Edward J. Anthony
Faraday Discussions | 2016
Jet Sing M. Lee; Gary T. Rochelle; Peter Styring; Paul S. Fennell; Grant Wilson; Martin Trusler; Peter T. Clough; John Blamey; Matthew T. Dunstan; Niall Macdowell; Stephen Lyth; Joseph Yao; Thomas Hills; Matteo Gazzani; Patrick Brandl; Rahul Anantharaman; Stefano Brandani; Joshuah K. Stolaroff; Marco Mazzotti; Geoffrey C. Maitland; Christoph R. Müller; George Dowson; Jon Gibbins; Raffaella Ocone; Kyra Sedransk Campbell; María Erans; Liya Zheng; Daniel Sutter; Andac Armutlulu; Berend Smit