Full exploitation and utilization of the unconventional reservoirs of shale gas have become a central issue due to the increasing worldwide energy demand. Enhancing shale gas recovery by injecting CO2 is a promising technique that combines shale gas extraction and CO2 capture and storage (CCS) perfectly. In this study, a kerogen-based slit-shaped pore with a width of ∼21 Å was constructed by two kerogen matrices, and the grand canonical Monte Carlo (GCMC) and molecular dynamics (MD) simulation methods were used to investigate the adsorption and diffusion properties of CH4 and CO2 in the kerogen matrix and slit nanopores and explore the displacement efficiency of the residual CH4 by CO2 in kerogen slit nanopores. The adsorption energy of CH4 and CO2 on the kerogen fragment surface and the isosteric heat of CH4 and CO2 in kerogen slit nanopores were examined to demonstrate the competitive adsorption of CO2 over CH4 in kerogen slit nanopores, and the different intensity of interactions between the CH4 and CO2 molecules with the pore surface plays a key role. An effective displacement process of the residual adsorbed CH4 by CO2 in kerogen slit nanopores was performed. The efficiency of displacement was enhanced with the increasing bulk pressure, and the sequestration amount of CO2 in kerogen slit nanopores increased at the same time. Moreover, it was found that part of CH4 adsorbed firmly inside the intrinsic pores of the kerogenmatrix was very hard to be displaced by the CO2 injection. This work demonstrates the microbehaviors of CH4 and CO2 in kerogen slit nanopores and the microscopic mechanism of the displacement of CH4 by CO2, for the purpose of providing useful guidance for enhancing shale gas extraction by injecting CO2.

Recently, bulk nanobubbles have attracted intensive attention due to the unique physicochemical properties and important potential applications in various fields. In this study, periodic pressure change was introduced to generate bulk nanobubbles. N2 nanobubbles with bimodal distribution and excellent stabilization were fabricated in nitrogen-saturated water solution. O2 and CO2 nanobubbles have also been created using this method and both have good stability. The influence of the action time of periodic pressure change on the generated N2 nanobubbles size was studied. It was interestingly found that, the size of the formed nanobubbles decreases with the increase of action time under constant frequency, which could be explained by the difference in the shrinkage and growth rate under different pressure conditions, thereby size-adjustable nanobubbles can be formed by regulating operating time. This study might provide valuable methodology for further investigations about properties and performances of bulk nanobubbles.

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The purpose of this study was to develop an in situ forming SAIB (sucrose acetate isobutyrate)-PLGA (poly (d, lactide-co-glycolide)) mixture matrix depot for sustained release of risperidone. The factors affecting the risperidone release kinetics were investigated to obtain further insight into the drug release mechanisms. The burst release in vitro was significantly reduced (4.95%) by using DMSO as solvent. And, increasing the PLGA content from 2 to 10% w/w decreased the initial release from 6.95 to 1.05%. The initial release in vivo decreased with increasing PLGA content (2.0% w/w PLGA, C(max) = 1161.7 ± 550.2 ng ml(-1); 10% w/w PLGA, C(max) = 280.3 ± 98.5 ng ml(-1)). The persistence (AUC(4-20 days)) over 20 days increased from 76.8 ± 20.7 to 362.8 ± 75.0 ng d ml(-1) by inclusion of 10% PLGA compared with the PLGA-free depot. These results demonstrate that the SAIB-PLGA mixture matrix depot could be useful as a sustained delivery system for risperidone.

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