Browsing by Author "Fennell, Paul S."
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Item Open Access Enhanced hydrogen production from thermochemical processes(Royal Society of Chemistry, 2018-07-24) Ji, Guozhao; Yao, Joseph G.; Clough, Peter T.; Diniz da Costa, João C.; Anthony, Edward J.; Fennell, Paul S.; Wang, Wei; Zhao, MingTo alleviate the pressing problem of greenhouse gas emissions, the development and deployment of sustainable energy technologies is necessary. One potentially viable approach for replacing fossil fuels is the development of a H2 economy. Not only can H2 be used to produce heat and electricity, it is also utilised in ammonia synthesis and hydrocracking. H2 is traditionally generated from thermochemical processes such as steam reforming of hydrocarbons and the water-gas-shift (WGS) reaction. However, these processes suffer from low H2 yields owing to their reversible nature. Removing H2 with membranes and/or extracting CO2 with solid sorbents in situ can overcome these issues by shifting the component equilibrium towards enhanced H2 production via Le Chatelier's principle. This can potentially result in reduced energy consumption, smaller reactor sizes and, therefore, lower capital costs. In light of this, a significant amount of work has been conducted over the past few decades to refine these processes through the development of novel materials and complex models. Here, we critically review the most recent developments in these studies, identify possible research gaps, and offer recommendations for future research.Item Open Access High CO2 absorption in new amine based-transition-temperature mixtures (deep eutectic analogues) and reporting thermal stability, viscosity and surface tension: Response surface methodology (RSM)(Elsevier, 2020-07-23) Ghaedi, Hosein; Zhao, Ming; Clough, Peter T.; Anthony, Ben; Fennell, Paul S.To study CO2 capture potential, three types of transition-temperature mixtures (TTMs) were prepared by mixing ethyltriphenylphosphonium bromide (MTPPB) as a hydrogen bond acceptor (HBA) and n-methyl diethanolamine (MDEA) as a hydrogen bond donor (HBD) in different molar ratios (1:7, 1:10 and 1:16). Fourier transform infrared spectroscopy (FT-IR) results showed that TTMs have almost similar spectra to their HBD (MDEA) with different levels of transmittance and exhibit similar behavior. From the experimental results, it was found that the thermal stability, viscosity and surface tension of TTMs decreased as the concentration of MDEA in the mixture increased. According to response surface methodology (RSM) models and analysis of variance (ANOVA), temperature and molar ratio had a great effect on the viscosity and surface tension of TTMs. Finally, it was found that CO2 solubility in TTMs (at 303.15 K at pressure up to 1.35 MPa) was enhanced as the MDEA quantity increased in the mixture up to 1:10 mol ratio. However, by increasing MDEA concentration to 16:1 mol ratio, there was a decreasing trend in the CO2 solubility data. Also, all TTMs, particularly TTM containing 10:1 mol MDEA (MTPPB-MDEA 1:10) exhibited an equilibrium loading capacity approaching 1 mol CO2 per mole solvent at high pressure, revealing their high potential for CO2 capture. A comparison showed that the CO2 solubility in the studied solvents was higher than that of existing deep eutectic solvents (DESs) and other TTMs as well as several ionic liquids (ILs) to date. To the best of our knowledge, this is the first study to report the CO2 solubility in phosphonium-base TTMs containing MDEAItem Open Access Hydrogen production by sorption enhanced steam reforming (SESR) of biomass in a fluidised-bed reactor using combined multifunctional particles(MDPI, 2018-05-21) Clough, Peter T.; Boot-Handford, Matthew E.; Zheng, Liya; Zhang, Zili; Fennell, Paul S.The performance of combined CO2-sorbent/catalyst particles for sorption enhanced steam reforming (SESR), prepared via a simple mechanical mixing protocol, was studied using a spout-fluidised bed reactor capable of continuous solid fuel (biomass) feeding. The influence of particle size (300–500 and 710–1000 µm), CaO loading (60–100 wt %), Ni-loading (10–40 wt %) and presence of dicalcium silicate support (22.6 wt %) on SESR process performance were investigated. The combined particles were characterised by their density, porosity and CO2 carrying capacity with the analysis by thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET), Barrett-Joyner-Halenda (BJH) and mercury intrusion porosimetry (MIP). All experiments were conducted with continuous oak biomass feeding at a rate of 0.9 g/min ± 10%, and the reactor was operated at 660 ± 5 °C, 1 atm and 20 ± 2 vol % steam which corresponds to a steam-to-carbon ratio of 1.2:1. Unsupported combined particles containing 21.0 wt % Ni and 79 wt % CaO were the best performing sorbent/catalyst particle screened in this study, when accounting for the cost of Ni and the improvement in H2 produced by high Ni content particles. SESR tests with these combined particles produced 61 mmol H2/gbiomass (122 g H2/kgbiomass) at a purity of 61 vol %. Significant coke formation within the feeding tube and on the surfaces of the particles was observed which was attributed to the low steam to carbon ratio utilised.Item Open Access Pilot testing of enhanced sorbents for calcium looping with cement production(Elsevier, 2018-05-26) Erans, María; Jeremias, Michal; Zheng, Liya; Yao, Joseph G.; Blamey, John; Manovic, Vasilije; Fennell, Paul S.; Anthony, Edward J.One of the main challenges for commercialising calcium looping (CaL) as a CO2 capture technology is maintaining a high level of sorbent reactivity during long-term cycling. In order to mitigate the decay in carrying capacity, research has moved towards producing enhanced sorbents. However, this creates potential problems related to ease of scaling up production techniques and production costs, and raises the question as to whether such approaches can be used at large scale. On the other hand, a key advantage of CaL over other carbon capture technologies is synergy with the cement industry, i.e., use of spent sorbent as a feedstock for clinker production. In this work two enhanced materials: (i) limestone doped with HBr through a particle surface impregnation technique; and (ii) pellets prepared from limestone and calcium aluminate cement, were tested in a 25 kWth dual fluidised bed pilot-scale reactor in order to investigate their capture performance and mechanical stability under realistic CaL conditions. Moreover, the spent sorbent was then used as a raw material to make cement, which was characterised for phase and chemical composition as well as compressive strength. The HBr-doped limestone showed better performance in terms of both mechanical strength and stability of the CO2 uptake when compared to that of pellets. Furthermore, it was shown that the cement produced has similar characteristics and performance as those of commercial CEM 1 cement. This indicates the advantages of using the spent sorbent as feedstock for cement manufacture and shows the benefits of synthetic sorbents in CaL and suitability of end-use of spent sorbents for the cement industry, validating their synergy at pilot scale. Finally, this study demonstrates the possibility of using several practical techniques to improve the performance of CaL at the pilot scale, and more importantly demonstrates that commercial-grade cement can be made from the lime product from this technology.Item Open Access Potassium carbonate-based ternary transition temperature mixture (deep eutectic analogues) for CO2 absorption: characterizations and DFT analysis(Springer, 2021-11-22) Ghaedi, Hosein; Kalhor, Payam; Zhao, Ming; Clough, Peter T.; Anthony, Edward J.; Fennell, Paul S.Is it possible to improve CO2 solubility in potassium carbonate (K2CO3)-based transition temperature mixtures (TTMs)? To assess this possibility, a ternary transition-temperature mixture (TTTM) was prepared by using a hindered amine, 2-amino-2-methyl-1,3-propanediol (AMPD). Fourier transform infrared spectroscopy (FT-IR) was employed to detect the functional groups including hydroxyl, amine, carbonate ion, and aliphatic functional groups in the prepared solvents. From thermogravimetric analysis (TGA), it was found that the addition of AMPD to the binary mixture can increase the thermal stability of TTTM. The viscosity findings showed that TTTM has a higher viscosity than TTM while their difference was decreased by increasing temperature. In addition, Eyring’s absolute rate theory was used to compute the activation parameters (∆G*, ∆H*, and ∆S*). The CO2 solubility in liquids was measured at a temperature of 303.15 K and pressures up to 1.8 MPa. The results disclosed that the CO2 solubility of TTTM was improved by the addition of AMPD. At the pressure of about 1.8 MPa, the CO2 mole fractions of TTM and TTTM were 0.1697 and 0.2022, respectively. To confirm the experimental data, density functional theory (DFT) was employed. From the DFT analysis, it was found that the TTTM + CO2 system has higher interaction energy (|∆E|) than the TTM + CO2 system indicating the higher CO2 affinity of the former system. This study might help scientists to better understand and to improve CO2 solubility in these types of solvents by choosing a suitable amine as HBD and finding the best combination of HBA and HBD.Item Open Access Progress in biofuel production from gasification(Elsevier, 2017-04-06) Sikarwar, Vineet Singh; Zhao, Ming; Fennell, Paul S.; Shah, Nilay; Anthony, Edward J.Biofuels from biomass gasification are reviewed here, and demonstrated to be an attractive option. Recent progress in gasification techniques and key generation pathways for biofuels production, process design and integration and socio-environmental impacts of biofuel generation are discussed, with the goal of investigating gasification-to-biofuels’ credentials as a sustainable and eco-friendly technology. The synthesis of important biofuels such as bio-methanol, bio-ethanol and higher alcohols, bio-dimethyl ether, Fischer Tropsch fuels, bio-methane, bio-hydrogen and algae-based fuels is reviewed, together with recent technologies, catalysts and reactors. Significant thermodynamic studies for each biofuel are also examined. Syngas cleaning is demonstrated to be a critical issue for biofuel production, and innovative pathways such as those employed by Choren Industrietechnik, Germany, and BioMCN, the Netherlands, are shown to allow efficient methanol generation. The conversion of syngas to FT transportation fuels such as gasoline and diesel over Co or Fe catalysts is reviewed and demonstrated to be a promising option for the future of biofuels. Bio-methane has emerged as a lucrative alternative for conventional transportation fuel with all the advantages of natural gas including a dense distribution, trade and supply network. Routes to produce H2 are discussed, though critical issues such as storage, expensive production routes with low efficiencies remain. Algae-based fuels are in the research and development stage, but are shown to have immense potential to become commercially important because of their capability to fix large amounts of CO2, to rapidly grow in many environments and versatile end uses. However, suitable process configurations resulting in optimal plant designs are crucial, so detailed process integration is a powerful tool to optimize current and develop new processes. LCA and ethical issues are also discussed in brief. It is clear that the use of food crops, as opposed to food wastes represents an area fraught with challenges, which must be resolved on a case by case basis.Item Open Access A shrinking core model for steam hydration of CaO-based sorbents cycled for CO2 capture(Rlsevier, 2016-02-01) Blamey, John; Zhao, Ming; Manovic, Vasilije; Anthony, Edward J.; Dugwell, Denis R.; Fennell, Paul S.Calcium looping is a developing CO2 capture technology. It is based on the reversible carbonation of CaO sorbent, which becomes less reactive upon cycling. One method of increasing the reactivity of unreactive sorbent is by hydration in the calcined (CaO) form. Here, sorbent has been subjected to repeated cycles of carbonation and calcination within a small fluidised bed reactor. Cycle numbers of 0 (i.e., one calcination), 2, 6 and 13 have been studied to generate sorbents that have been deactivated to different extents. Subsequently, the sorbent generated was subjected to steam hydration tests within a thermogravimetric analyser, using hydration temperatures of 473, 573 and 673 K. Sorbents that had been cycled less prior to hydration hydrated rapidly. However, the more cycled sorbents exhibited behaviour where the hydration conversion tended towards an asymptotic value, which is likely to be associated with pore blockage. This asymptotic value tended to be lower at higher hydration temperatures; however, the maximum rate of hydration was found to increase with increasing hydration temperature. A shrinking core model has been developed and applied to the data. It fits data from experiments that did not exhibit extensive pore blockage well, but fits data from experiments that exhibited pore blockage less well.