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Photocatalytic hydrogen production is considered a promising approach to generating clean sustainable energy. However, the conventional co-catalyst (e.g., Pt) used in photocatalytic hydrogen production is high-cost and difficult to obtain. Here, we designed and prepared a ternary nanocomposite MXene@Au@CdS, which can be used in the field of efficient and excellent photocatalytic hydrogen production. The MXene@Au@CdS has a hydrogen production rate of 17,070.43 μmol g−1 h−1 (tested for 2 h), which is 1.85 times that of pure CdS nanomaterials. The improved hydrogen production performance of the MXene@Au@CdS is attributed to: (i) MXene provides more active adsorption sites and reaction centers for Au and CdS nanoparticles; (ii) the synergistic effect of Au’s strong surface plasmon resonance expands the optical response range of CdS. Therefore, this work solves the problem of the solid connection between the surface functional groups of photocatalyst, and achieves rapid interface charge transfer and long-term stability during the hydrogen production.

Arsenic decontamination from groundwater is an urgent but still challenging task. Polystyrene-based hydrated ferric oxide (denoted as D201-HFO) nanocomposite is a new emerging current adsorbent for efficient arsenate removal in natural waters; the resulting materials can interact with arsenate, mainly driven by inner complexation and static interaction and the existing HA effects on adsorption was well investigated. Results reveals that low concentrations of HA (below 25 mg/L) coexistence led to negligible effects on As(V) removal, but high levels of HA (100 mg/L) exerted outstanding sorption competition to As(V) removal; kinetics results revealed the HA additions brought about the diffusion prolonging and capacity decline, due to the large molecule structure of HA. Column experiments further showed the slight decrease application capacity of 810 BV by HA additions, with satisfactory saturation capacity; significantly, the presence of HA also exerted negligible influences on regeneration performances. All the sorbents with or without HA could be well regenerated by binary alkaline and salt mixture.

Graphene oxide (GO)-chitosan composite hydrogels were successfully prepared via the self-assembly of chitosan molecules and GO. These as-prepared hydrogels were characterized by different techniques. The morphology of the internal network structure of the nanocomposite hydrogels was investigated. The adsorption capacity results demonstrate that the prepared GObased composite hydrogels can efficiently remove three tested dye molecules, Congo red, methylene blue and Rhodamine B, from wastewater in accordance with the pseudo-second-order model. The dye adsorption capacity of the obtained hydrogels is mainly attributed to the GO sheets, whereas the chitosan molecule was incorporated to facilitate the gelation process of the GO sheets. The present study indicates that the as-prepared composite hydrogels can serve as good adsorbents for wastewater treatment as well as the removal of harmful dyes.

Here we present a simple and convenient sticky/blunt-end ligation method for fusion gene construction. The fusion gene is constructed by seamless ligation of 5'-end phosphorylated blunt ends instead of by overlap extension PCR (OE-PCR). Therefore, the challenge of amplifying large DNA fragments (e.g., the large bifunctional enzyme gene constructed by fusion of two monofunctional enzyme genes) by PCR can be avoided. In addition, synthesis of the inner primers for OE-PCR is not necessary, indicating that this method should be especially convenient for construction of fusion genes with various combinations of multiple fragments (e.g., chimeric gene libraries, fusion gene libraries). As a modification of the commonly used fusion gene construction technique, this method may find a wide range of applications in bioscience and biotechnology.

Four achiral Cu(II)-coordinated Schiff bases complexes containing aromatic structures were synthesized and their supramolecular assemblies at the air/water interface were investigated. All the compounds could be spread on water surface although they have no alkyl chains. The Schiff base complex molecules with naphthyl groups tended to form J-aggregate in the Langmuir-Blodgett (LB) films transferred from water surface. By investigation of atomic force microscopy, a multilayer film or three-dimensional structures were observed. It was interesting to note that the LB films of achiral compound Cu-NA with naphthyl segment and without methyl groups transferred from water surface showed chirality. The supramolecular chirality in the present LB films was suggested to be due to a cooperative stereoregular π-π stacking of the functional groups in a helical sense. This research work provides a helpful clue for regulating the nanostructures and supramolecular chiral assembly in organized films.

By encapsulating zirconium phosphate (ZrP) nanoparticles into three macroporous polystyrene resins with various surface groups, i.e., −CH2Cl, −SO3 −, and −CH2N+(CH3)3 three nanocomposite adsorbents (denoted as ZrP–Cl, ZrP–S, and ZrP–N) were fabricated, respectively for lead removal from water. Effect of the functional groups on nano-ZrP dispersion and effect of ZrP immobilization on the mechanical strength of the resulting nanocomposites were investigated. The presence of the charged functional groups (−SO3 − and −CH2N+(CH3)3) are more favorable than the neutral −CH2Cl group to improve nano-ZrP dispersion (i.e., to achieve smaller ZrP nanoparticles). ZrP–N and ZrP–S had higher capacity than ZrP–Cl for lead removal. As compared to ZrP–N, ZrP–S exhibits higher preference toward lead ion at high calcium levels as a result of the potential Donnan membrane effect. On the other hand, nano-ZrP immobilization would simultaneously reinforce both the compressive strength and the wear performance of the resulting nanocomposites with the ZrP loadings up to 5 wt%. The results reported herein would shed some light on the generation of environmental nanocomposites with high capacity and excellent mechanical strength.

The knowledge of the mechanism of flux distribution will benefit understanding cell physiology and regulation of metabolism. In this study, the measured fluxes obtained under steady-state conditions were used to estimate intracellular fluxes and identify the robustness of branch points of the anaerobic glycerol metabolism in Klebsiella pneumoniae for the production of 1,3-propanediol by metabolic flux analysis. The biomass concentration increased as NADH(2)/NAD(+) decreased at low initial concentration and inversed at high initial glycerol concentration. The flux distribution revealed that the branch points of glycerol and dihydroxyacetonephosphate were rigid to the environmental conditions. However, the pyruvate and acetyl coenzyme A metabolisms gave cells the flexibility to regulate the energy and intermediate fluxes under various environmental conditions. Additionly, it was found that the formation rate of ethanol and the ratio of pyruvate dehydrogenase to pyruvate formate lyase appeared visible fluctuations at high glycerol uptake rate.

New reduced graphene oxide-based silver nanoparticle-containing composite hydrogels were successfully prepared in situ through the simultaneous reduction of GO and noble metal precursors within the GO gel matrix. The as-formed hydrogels are composed of a network structure of cross-linked nanosheets. The reported method is based on the in situ co-reduction of GO and silver acetate within the hydrogel matrix to form RGO-based composite gel. The stabilization of silver nanoparticles was also achieved simultaneously within the gel composite system. The as-formed silver nanoparticles were found to be homogeneously and uniformly dispersed on the surface of the RGO nanosheets within the composite gel. More importantly, this RGO-based silver nanoparticle-containing composite hydrogel matrix acts as a potential catalyst for removing organic dye pollutants from an aqueous environment. Interestingly, the as-prepared catalytic composite matrix structure can be conveniently separated from an aqueous environment after the reaction, suggesting the potentially large-scale applications of the reduced graphene oxide-based nanoparticle-containing composite hydrogels for organic dye removal and wastewater treatment.

Graphene oxide (GO) sheets exhibit superior adsorption capacity for removing organic dye pollutants from an aqueous environment. In this paper, the facile preparation of GO/polyethylenimine (PEI) hydrogels as efficient dye adsorbents has been reported. The GO/PEI hydrogels were achieved through both hydrogen bonding and electrostatic interactions between amine-rich PEI and GO sheets. For both methylene blue (MB) and rhodamine B (RhB), the as-prepared hydrogels exhibit removal rates within about 4 h in accordance with the pseudo-second-order model. The dye adsorption capacity of the hydrogel is mainly attributed to the GO sheets, whereas the PEI was incorporated to facilitate the gelation process of GO sheets. More importantly, the dye-adsorbed hydrogels can be conveniently separated from an aqueous environment, suggesting potential large-scale applications of the GO-based hydrogels for organic dye removal and wastewater treatment.