Please cite this article in press as: Liang, Z., et al., Recent progress and new developments in post-combustion carbon-capture technology with amine based solvents. Int. J. Greenhouse Gas Control (2015), http://dx.Keywords: Recent development of PCC process Design and modeling Solvent development Post Build Operations Solvent chemistry Solvent management Mass transfer with reaction a b s t r a c tCurrently, post-combustion carbon capture (PCC) is the only industrial CO 2 capture technology that is already demonstrated at full commercial scale in the TMC Mongstad in Norway (300,000 tonnes per year CO 2 captured) and BD3 SaskPower in Canada (1 million tonnes per year CO 2 captured). This paper presents a comprehensive review of the most recent information available on all aspects of the PCC processes. It provides designers and operators of amine solvent-based CO 2 capture plants with an in-depth understanding of the most up-to-date fundamental chemistry and physics of the CO 2 absorption technologies using amine-based reactive solvents. Topics covered include chemical analysis, reaction kinetics, CO 2 solubility, and innovative configurations of absorption and stripping columns as well as information on technology applications. The paper also covers in detail the post build operational issues of corrosion prevention and control, solvent management, solvent stability, solvent recycling and reclaiming, intelligent monitoring and plant control including process automation. In addition, the review discusses the most up-to-date insights related to the theoretical basis of plant operation in terms of thermodynamics, transport phenomena, chemical reaction kinetics/engineering, interfacial phenomena, and materials. The insights will assist engineers, scientists, and decision makers working in academia, industry and government, to gain a better appreciation of the post combustion carbon capture technology.
In this study, we report a promising rGO-CNT hybrid nanofiltration (NF) membrane that was fabricated by loading reduced graphene oxide that was intercalated with carbon nanotubes (rGO-CNTs) onto an anodic aluminum oxide (AAO) microfiltration membrane via a facile vacuum-assisted filtration process. To create this NF membrane, the CNTs were first dispersed using block copolymers (BCPs); the effects of the types and contents of BCPs used on the dispersion of CNTs have been investigated. The as-prepared rGO-CNT hybrid NF membranes were then used for drinking water purification to retain the nanoparticles, dyes, proteins, organophosphates, sugars, and particularly humic acid. Experimentally, it is shown that the rGO-CNT hybrid NF membranes have high retention efficiency, good permeability and good anti-fouling properties. The retention was above 97.3% even for methyl orange (327 Da); for other objects, the retention was above 99%. The membrane's permeability was found to be as high as 20-30 L m(-2) h(-1) bar(-1). Based on these results, we can conclude that (i) the use of BCPs as a surfactant can enhance steric repulsion and thus disperse CNTs effectively; (ii) placing well-dispersed 1D CNTs within 2D graphene sheets allows an uniform network to form, which can provide many mass transfer channels through the continuous 3D nanostructure, resulting in the high permeability and separation performance of the rGO-CNT hybrid NF membranes.
The mass-transfer performance of CO2 absorption
into
aqueous diethylenetriamine (DETA) solutions was investigated in an
absorption column randomly packed with Dixon rings at 303–303
K and atmospheric pressure, and compared with that of monoethanolamine
(MEA), which is widely considered as a benchmark solvent for CO2 absorption. The mass-transfer performance was presented in
terms of volumetric overall mass-transfer coefficient (K
G
a
v). In particular, the effects
of operating parameters, such as inlet CO2 loading, solvent
concentration, liquid flow rate, inert gas flow rate, and liquid temperature,
were investigated and compared for both MEA and DETA. Over 40 runs
of absorption experiments were carried out in this study. The results
showed that K
G
a
v of DETA was found to be higher than that of MEA. Also, inlet CO2 loading, solvent concentration, liquid flow rate, and liquid
inlet temperature had significant effect on K
G
a
v for both systems. However,
the inert gas flow rate had an insignificant effect on K
G
a
v. Lastly, predictive correlations
for K
G
a
v for
DETA–CO2 and MEA–CO2 systems in
randomly Dixon ring packed columns were successfully developed. The
predicted results were found to be in relatively good agreement with
the experimental results, with average absolute deviations (AADs)
of 16% and 14%, respectively.
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