Experimental Study on the Interplay between Different Brine Types/Concentrations and CO2 Injectivity for Effective CO2 Storage in Deep Saline Aquifers

Salt precipitation during CO2 storage in deep saline aquifers can have severe consequences on injectivity during carbon storage. Extensive studies have been carried out on CO2 solubility with individual or mixed salt solutions; however, to the best of the authors’ knowledge, there is no substantial study to consider pressure decay rate as a function of CO2 solubility in brine, and the range of brine concentration for effective CO2 storage. This study presents an experimental core flooding of the Bentheimer sandstone sample under simulated reservoir conditions to examine the effect of four different types of brine at a various ranges of salt concentration (5 to 25 wt.%) on CO2 storage. Results indicate that porosity and permeability reduction, as well as salt precipitation, is higher in divalent brines. It is also found that, at 10 to 20 wt.% brine concentrations in both monovalent and divalent brines, a substantial volume of CO2 is sequestered, which indicates the optimum concentration ranges for storage purposes. Hence, the magnitude of CO2 injectivity impairment depends on both the concentration and type of salt species. The findings from this study are directly relevant to CO2 sequestration in deep saline aquifers as well as screening criteria for carbon storage with enhanced gas and oil recovery processes.

Degradation Behaviors of Two Epoxy Coatings After Dry/Wet-Accelerated Fog Exposure of Different Solutions

Applying organic coating is an important and effective approach for the protection of metal from corrosion. Weathering degradation and under-film corrosion are the two major important factors that cause the failure of organic coatings. In this work, the degradation investigation of two epoxy coatings (clear and pigmented coatings) was carried out under the dry–wet circulation of three different water fog solutions (deionized water, 0.5 wt% NaCl, 0.05 wt% NaCl + 0.35 wt% (NH4)2SO4) in 35 days. The apparent performance (pull-off adhesion and surface potentials) and electrochemical features [electrochemical noise and electrochemical impedance spectroscopy (EIS)] of the coating samples were monitored after dry–wet fog exposure. In our three accelerating systems of the fog atmosphere, the time that the detectable defects appeared on the surface of coating samples was far ahead in the mixed salt solution than that in the deionized water or 0.5 wt% NaCl solution. For a defective or damaged coating surface, the derived results by using the standard deviation method (SDM) or Fourier power spectrum (FPS) were rather higher than those obtained from EIS as a whole, while for the same coating, the degradation trend with time derived from EIS, SDM, FPS, and scanning Kelvin probe was consistent with each other.

Engineering Li/Na selectivity in 12-Crown-4–functionalized polymer membranes

Lithium is widely used in contemporary energy applications, but its isolation from natural reserves is plagued by time-consuming and costly processes. While polymer membranes could, in principle, circumvent these challenges by efficiently extracting lithium from aqueous solutions, they usually exhibit poor ion-specific selectivity. Toward this end, we have incorporated host–guest interactions into a tunable polynorbornene network by copolymerizing 1) 12-crown-4 ligands to impart ion selectivity, 2) poly(ethylene oxide) side chains to control water content, and 3) a crosslinker to form robust solids at room temperature. Single salt transport measurements indicate these materials exhibit unprecedented reverse permeability selectivity (∼2.3) for LiCl over NaCl—the highest documented to date for a dense, water-swollen polymer. As demonstrated by molecular dynamics simulations, this behavior originates from the ability of 12-crown-4 to bind Na+ ions more strongly than Li+ in an aqueous environment, which reduces Na+ mobility (relative to Li+) and offsets the increase in Na+ solubility due to binding with crown ethers. Under mixed salt conditions, 12-crown-4 functionalized membranes showed identical solubility selectivity relative to single salt conditions; however, the permeability and diffusivity selectivity of LiCl over NaCl decreased, presumably due to flux coupling. These results reveal insights for designing advanced membranes with solute-specific selectivity by utilizing host–guest interactions.

Impact of sulfate on the solubility of Tc(IV) in acidic to hyperalkaline aqueous reducing systems

The solubility of 99Tc(IV) was investigated from undersaturation conditions in NaCl–Na2SO4 (0.3 M ≤ I ≤ 5.0 M), MgCl2–MgSO4 (I = 13.5 M) and CaCl2–CaSO4 (I = 13.5 M) systems with 0.001 M ≤ [SO4 2−]tot ≤ 1.0 M and 1 ≤ pH m ≤ 12 (with pH m = −log[H+], in molal units). Reducing conditions were set by either Sn(II) or Fe(0). Special efforts were dedicated to accurately characterize the correction factors A m required for the determination of pH m from the experimentally measured pH values in the mixed salt systems investigated, with pH m = pHexp + A m . The combination of (pe + pH m ) measurements with Pourbaix diagrams of Tc suggests that technetium is present in its +IV redox state. This hypothesis is confirmed by XANES, which unambiguously shows the predominance of Tc(IV) both in the aqueous and solid phases of selected solubility samples. XRD and SEM–EDS support the amorphous character of the solid phase controlling the solubility of Tc(IV). EXAFS data confirm the predominance of TcO2(am, hyd) at pH m > 1.5, whereas the formation of a Tc(IV)–O–Cl solid phase is hinted at lower pHm values in concentrated NaCl–Na2SO4 systems with ≈5 M NaCl. Solubility data collected in sulfate-containing systems are generally in good agreement with previous solubility studies conducted in sulfate-free NaCl, MgCl2 and CaCl2 solutions of analogous ionic strength. Although the complexation of Tc(IV) with sulfate cannot be completely ruled out, these results strongly support that, if occurring, complexation must be weak and has no significant impact on the solubility of Tc(IV) in dilute up to highly saline media. Solubility upper-limits determined in this work can be used for source term estimations including the effect of sulfate in a variety of geochemical conditions relevant in the context of nuclear waste disposal.

Passivation Strategies through Surface Reconstruction toward Highly Efficient and Stable Perovskite Solar Cells on n-i-p Architecture

Perovskite solar cells have achieved remarkable enhancement in their performance in recent years. However, to get an entrance to the photovoltaic market, great effort is still necessary to further improve their efficiency as well as their long-term stability under various conditions. Among various types of approaches (including compositional engineering, dopant engineering, self-assembled monolayers (SAMs), et al.), interfacial engineering through passivation treatment has been considered as one of the most effective strategies to reduce the non-radiative recombination within the PSCs. Thus, this short review summaries recent efforts on chemical interfacial passivation strategies from a different perspective owing to their common phenomena of reconstructing the perovskite surface via the formation of three-dimensional perovskite, low-dimensional perovskite and synergistic effect provided by a mixed-salt passivation system, respectively.