A one-dimensional (1D) core-shell of Co-Ce oxide has been prepared by multifluidic coaxial electrospinning method and evaluated for the total oxidation of propane (C3H8). Activity and morphological characterizations show that the CeO2@Co3O4 nanofiber catalyst, of which the core is CeO2 and the shell is Co3O4, exhibits excellent oxidation activity. The exposed Co3O4 grown on the outside of the fibers can rapidly react with C3H8 while CeO2 with high oxygen storage capacity in the inside is conductive to the enhanced oxidation rate. Besides, the continuous grain boundary provides a fast mass transfer channel for lattice oxygen, and rich oxygen vacancies favor the mobility of active oxygen species. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTs) confirms that the CeO2@Co3O4 catalyst have a faster rate of C3H8 adsorption and better oxidation activity with respect to the counterpart using a single-needle electrospinning method. Moreover, the CeO2@Co3O4 catalyst displays excellent thermal stability, and strong resistance against 5 vol% H2O and 5 vol% CO2 at both 300 and 400 °C. Our strategy can give some new insights into morphological engineering to promote active oxygen mobility via the construction of one-dimensional core-shell of metal oxides for catalytic oxidation of VOCs.Halloysite nanotubes (HNTs) as a natural and inexpensive clay mineral with hollow nanotubular structures, good biocompatibility and active surfaces have been ubiquitously applied in many fields. In this work, a novel multifunctional core-shell sorbent based on HNTs, CuCl2-HNTs encapsulated magnetic microspheres (SiO2@Fe3O4), was successfully fabricated and applied for Hg0 removal from flue gas with good performance for the first time. The core-shell structure prevented the composites from aggregating but kept their magnetism, which enabled the adsorbents being easily separated for reuse by an external magnetic field. In addition, the special structure also significantly enhanced the adsorption capacity of the composites by dispersing the CuCl2 modified HNTs on the prepared magnetic microspheres. The adsorption performance was comprehensively investigated and fitted by dynamic models. The adsorption followed surface adsorption, particle diffusion and chemisorption with very good SO2 tolerance. The Cu+, Cl- and lattice oxygen were the crucial components for Hg0 removal. MK-8776 in vitro In order to further understand the possible mechanism, an online home-made coupling system of temperature-programmed decomposition (TPD) was used to investigate the mercury species on the spent adsorbent in addition to X-ray photoelectron spectroscopy analysis. The results confirmed the mercury species adsorbed were primarily Hg0, HgO and HgCl2.Microgravimetric sensor platforms with physico- or chemo-selective interfaces offer promising sensing properties. They are widely used to detect chemical warfare agents (CWAs). However, a comprehensive insight into adsorption mechanisms and interactions between low concentrations of these adsorbates and low-mass adsorbents is still lacking. In this study, we report a complete and detailed analytical method to model the adsorption processes of low traces of vapor-phase DiMethyl MethylPhosphonate (DMMP), a conventional simulant of CWAs, on a double-side nanostructured microcantilever coated with vertically-aligned titanium dioxide nanotubes (TiO2-NTs). We find that the geometrical configuration of NTs plays an important role in the diffusion regimes of molecules during the adsorption. This study shines light on the adsorption and kinetic mechanisms of low-traces DMMP offering opportunities to have a better insight of the adsorption of CWAs on complex nanostructures and to improve microcantilever sensors.Improving biomass enzymatic saccharification is effective for crop straw utilization, whereas phytoremediation is efficient for trace metal elimination from polluted agricultural soil. Here, we found that the green proteins extracted from Amaranthus leaf tissue could act as active biosurfactant to remarkably enhance lignocellulose enzymatic saccharification for high bioethanol production examined in eight grassy and woody plants after mild chemical and green-like pretreatments were performed. Notably, this study estimated that total green proteins supply collected from one-hectare-land Amaranth plants could even lead to additional 6400-12,400 tons of bioethanol, being over 10-fold bioethanol yield higher than those of soybean seed proteins and chemical surfactant. Meanwhile, the Amaranth green proteins were characterized as a dominated biosorbent for multiple trace metals (Cd, Pb, As) adsorption, being 2.9-6 folds higher than those of its lignocellulose. The Amaranth plants were also assessed to accumulate much more trace metals than all other plants as previously examined from large-scale contaminated soils. Furthermore, the Amaranth green proteins not only effectively block lignin to release active cellulases for the mostly enhanced biomass hydrolyzes, but also efficiently involve in multiple chemical bindings with Cd, which should thus address critical issues of high-costly biomass waste utilization and low-efficient trace metal remediation.Iron is one of the essential trace elements in the human body, which is involved in many important physiological processes of life. The abnormal amount of iron in the body will bring many diseases. Therefore, a novel near-infrared fluorimetric method was developed. The method is based on a fluorescent probe (E)-4-(2-(3-(dicyanomethylene)-5,5-dimethylcyclohex-1-en-1-yl)vinyl)-N, N-diethylaniline oxide (DDED) which uses N-oxide as a recognition group to real-time monitoring and imaging of Fe2+ in vivo and in vitro. The method exhibits excellent selectivity and high sensitivity (LOD = 27 nM) for Fe2+, fast reaction rate ( less then 4 min), extremely large Stokes shift (＞ 275 nm), low cytotoxicity. The strip test strongly illustrates the potential application of DDED in real environment. In particular, DDED has been successfully applied to real-time monitoring and imaging of Fe2+ in HepG2 cells and zebrafish. That is, the method has great potential for the detection of Fe2+ in living systems.