Abstract:We have conducted comprehensive exergy analyses of three integrated gasification combined cycle with carbon capture and storage (IGCC-CCS) power plant configurations: (1) a baseline model using Selexol™ for H 2 S/CO 2 removal; (2) a modified version that adds a H 2 -selective membrane before the Selexol™ acid gas removal system; and (3) a modified baseline version that uses a CO 2 -selective membrane before the Selexol™ acid gas removal system. While holding the coal input flow rate and the CO 2 captured flow rates constant, it was determined that the H 2 -selective membrane case had a higher net power output (584 MW) compared to the baseline (564 MW) and compared to the CO 2 -selective membrane case (550 MW). Interestingly, the CO 2 -selective membrane case destroyed the least amount of exergy within the power plant (967 MW), compared with the Baseline case (999 MW) and the H 2 -membrane case (972 MW). The main problem with the CO 2 -selective membrane case was the large amount of H 2 (48 MW worth of H 2 chemical exergy) remaining within the supercritical CO 2 that exits the power plant. Regardless of the CO 2 capture process used, the majority of the exergy destruction occurred in the gasifier (305 MW) and gas turbine (~380 MW) subsystems, suggesting that these two areas should be key areas of focus of future improvements.

miRNA is a promising class of biomarkers whose levels can be assayed to detect various forms of cancer and other serious diseases. These short, noncoding nucleic acids are difficult to detect due to their low abundance and the marginal stability of their duplexes with DNA probes. In addition, miRNAs within the same family have high sequence homology, and often, related miRNA differ in sequence by only a single base. In this report, we demonstrate an independent detection seven members of the let‐7 family of miRNA in a single run. Key to success is the use of mini‐PEG‐substituted PNA amphiphiles (γPNAA) and highly fluorescent DNA nanotags in micelle tagging electrophoresis (MTE). Multiplexed detection is accomplished in capillary electrophoresis (CE) using oligomeric nanotags of pre‐programmed lengths where the presence of a specific miRNA links its nanotag to a micelle drag‐tag, which shifts the nanotag elution time to a defined region for detection. We further demonstrate that the peak shape and elution time are unaffected by the presence of up to 10 mg/ml of serum protein in the sample, with a total runtime of less than 4 min and a LOD of 10–100 pM. We discuss efforts to substantially decrease the detection limit using nanotags that are >1000 bp in length.