CO2 electrolysis is a key step in CO2 conversion into fuels and chemicals as a way of mitigating climate change. We report the synthesis and testing of a series of new anion‐conductive membranes (tradenamed Sustainion™) for use in CO2 electrolysis. These membranes incorporate the functional character of imidazolium‐based ionic liquids as co‐catalysts in CO2 reduction into a solid membrane with a styrene backbone. We find that the addition of an imidazolium group onto the styrene side‐chains increases the selectivity of the reaction from approximately 25 % to approximately 95 %. The current at 3 V is increased by a factor of 14. So far we have been able to tune these parameters to achieve stable cells that provide current densities higher than 100 mA cm−2 at 3 V cell potential with a CO product selectivity over 98 %. Stable performance was observed for 6 months of continuous operation (>150 000 000 turnovers). These results demonstrate that imidazolium polymers are ideal membranes for CO2 electrolysis.

We report a modular construction of a new metal-organic framework (MOF) by strategically incorporating a number of water repellent functional groups in the frameworks. These MOFs demonstrate both open structure for high sorption capability and strong water resistance.

Intercalation of polysulfides into LDHs forms layered composites that can separate Hg2+, Ag+ and Cu2+ from mixed ions with high selectivity and capacity.

BackgroundThe Hepatitis C virus (HCV) core protein has been implicated as a potential oncogene or a cofactor in HCV-related hepatocellular carcinoma (HCC), but the underlying mechanisms are unknown. Overactivation of the Wnt/β-catenin signaling is a major factor in oncogenesis of HCC. However, the pathogenesis of HCV core-associated Wnt/β-catenin activation remains to be further characterized. Therefore, we attempted to determine whether HCV core protein plays an important role in regulating Wnt/β-catenin signaling in HCC cells.MethodologyWnt/β-catenin signaling activity was investigated in core-expressing hepatoma cells. Protein and gene expression were examined by Western blot, immunofluorescence staining, RT-qPCR, and reporter assay.Principal FindingsHCV core protein significantly enhances Tcf-dependent transcriptional activity induced by Wnt3A in HCC cell lines. Additionally, core protein increases and stabilizes β-catenin levels in hepatoma cell line Huh7 through inactivation of GSK-3β, which contributes to the up-regulation of downstream target genes, such as c-Myc, cyclin D1, WISP2 and CTGF. Also, core protein increases cell proliferation rate and promotes Wnt3A-induced tumor growth in the xenograft tumor model of human HCC.Conclusions/SignificanceHCV core protein enhances Wnt/β-catenin signaling activity, hence playing an important role in HCV-associated carcinogenesis.

A B S T R A C TThe electrochemical production of syngas would enable production of chemicals and transportation fuels from carbon dioxide, water and renewable energy, but a suitable process at the moment does not exist. In this paper we consider two options for syngas production: (i) CO 2 electrolysis to produce CO, water electrolysis to produce H 2 and then mixing the CO and H 2 to yield syngas; and (ii) the simultaneous coelectrolysis of CO 2 and H 2 O in a single electrolyzer. The results show that both processes can produce syngas at industrially important rates. In this paper we demonstrate CO 2 electrolysis at 100 mA/cm 2 , i.e., about 20 turnovers/s, and water electrolysis at 8 A/cm 2 at 2.0 V/cell, with about 1,600 turnovers/s. Both systems are stable for a thousand hours or more, i.e., millions of turnovers. We also demonstrate simultaneous CO and H 2 production in a single electrolyzer. These results demonstrate that syngas can be produced at industrially important rates via electrolysis.