We report herein a facile method for the preparation of sodium tungsten bronzes hollow nanospheres using hydrogen gas bubbles as reactant for chemical reduction of tungstate to tungsten and as template for the formation of hollow nanospheres at the same time. The chemical composition and the crystalline state of the as-prepared hollow Na0.15WO3nanospheres were characterized complementarily, and the hollow structure formation mechanism was proposed. The hollow Na0.15WO3nanospheres showed large Brunauer-Emment-Teller specific area (33.8 m2 g-1), strong resistance to acids, and excellent ability to remove organic molecules such as dye and proteins from aqueous solutions. These illustrate that the hollow nanospheres of Na0.15WO3should be a useful adsorbent.

Oil sediment interactions play an important role in the formation of submerged oils in coastal marine environments. Thus, the formation processes of submerged oils under the effect of suspended sediments were investigated in this study. Batch experiments were conducted to assess the role of adsorption processes on the suspended sediments in controlling levels of formation of submerged oils using three kind of Bohai crude oils [obtained from the Liaohe oilfield (LX), Bohai south regional oilfield (YYH) and Bohai central regional oilfield (YYS)]. The results showed that the saturated adsorption capacities by sandy sediments were 568, 429 and 352 mg g-1 for LX, YYH and YYS, respectively. Kinetic studies showed that the adsorption rate was about 0.002 mg g-1 min-1 in the first 200 minutes, and the maximum proportion of the submerged oils formed was 43%, 40% and 34% for LX, YYH and YYS, respectively. Partitioning of oils occurs between solid and solution phases during the oil sediment interactions, and always involving a distribution coefficient (K d). Importantly, an adsorption model was proposed in this study for predicting the formation of submerged oils with most of the experimental data fitting the model defined by a zone with K d values of 0.5 and 1.5 mL mg-1. Those results can help assess the fate and distribution of oil leakages in marine environments.

This paper reports on a novel method to remove Hg0 in the wet scrubbing process using defect-rich colloidal copper sulfides for reducing mercury emissions from non-ferrous smelting flue gas. Unexpectedly, it migrated the negative effect of SO2 on mercury removal performance, while also enhancing Hg0 adsorption. Colloidal copper sulfides demonstrated the superior Hg0 adsorption rate of 306.9 μg·g-1·min-1 under 6% SO2 + 6% O2 atmosphere with a removal efficiency of 99.1%, and the highest-ever Hg0 adsorption capacity of 736.5 mg·g-1, which was 277% higher than all other reported metal sulfides. The Cu and S sites transformation results reveal that SO2 could transform the tri-coordinate S sites into S22- on copper sulfides surfaces, while O2 regenerated Cu2+ via the oxidation of Cu+. The S22- and Cu2+ sites enhanced Hg0 oxidation, and the Hg2+ could strongly bind with tri-coordinate S sites. This study provides an effective strategy to achieve large-capability adsorption of Hg0 from non-ferrous smelting flue gas.

Novel PEGylated thermo-sensitive bionic magnetic core-shell structure molecularly imprinted polymers (PMMIPs) for the specific adsorption and separation of bovine serum albumin (BSA) were obtained via a surface-imprinting technique. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), fourier transform infrared spectrometry (FT-IR), thermal gravimetric analysis (TGA), and specific surface area (BET), were adopted to demonstrate that novel PMMIPs were successfully synthesized. Subsequently, the prepared PMMIPs were used as the extractor for BSA and were combined with magnetic solid-phase extraction. The concentrations of BSA were detected by UV-vis spectrophotometry at 278 nm. The maximum adsorption capacity of the PMMIPs was 258 mg g-1, which is much higher than that of non-imprinted polymer (PMNIPs). PMMIPs showed favorable selectivity for BSA against reference proteins, i.e., bovine hemoglobin, ovalbumin and lysozyme. PMMIPs were further used to recognize BSA in protein mixtures, milk, urine and sewage, these results revealed that approximately 96% of the ideal-state adsorption capacity of PMMIPs for BSA was achieved under complicated conditions. Regeneration and reusability studies demonstrated that adsorption capacity loss of the PMMIPs was not obvious after recycling for four times. Facile synthesis, excellent adsorption property and efficient selectivity for BSA trapping are features that highlight PMMIPs as an attractive candidate for biomacromolecular purification.

Damage to vascular endothelial cells (VECs) is a critical hallmark of hemorrhagic diseases caused by dengue virus (DENV). However, the precise molecular event involved in DENV binding and infection of VECs has yet to be clarified. In this study, vimentin (55 kDa) was identified to be involved in DENV-2 adsorption into VECs. This protein is located on the surface of VECs and interacts with DENV-2 envelope protein domain III (EDIII). The expression level of the superficial vimentin on VECs was not affected by viral infection or siRNA interference, indicating that the protein exists in a particular mode. Furthermore, the rod domain of the vimentin protein mainly functions in DENV-2 adsorption into VECs. Molecular docking results predicted several residues in vimentin rod and DENV EDIII; these residues may be responsible for cell-virus interactions. We propose that the superficial vimentin could be a novel molecule involved in DENV binding and infection of VECs. DENV EDIII directly interacts with the rod domain of vimentin on the VEC surface and thus mediates the infection.

Oxygen-containing functional groups were found to effectively boost the K+ storage performance of carbonaceous materials, however, the mechanism behind the performance enhancement remains unclear. Herein, we report higher rate capability and better long-term cycle performance employing oxygen-doped graphite oxide (GO) as the anode material for potassium ion batteries (PIBs), compared to the raw graphite. The in situ Raman spectroscopy elucidates the adsorption-intercalation hybrid K+ storage mechanism, assigning the capacity enhancement to be mainly correlated with reversible K+ adsorption/desorption at the newly introduced oxygen sites. It is unraveled that the C=O and COOH rather than C-O-C and OH groups contribute to the capacity enhancement. Based on in situ Fourier transform infrared (FT-IR) spectra and in situ electrochemical impedance spectroscopy (EIS), it is found that the oxygen-containing functional groups regulate the components of solid electrolyte interphase (SEI), leading to the formation of highly conductive, intact and robust SEI. Through the systematic investigations, we hereby uncover the K+ storage mechanism of GO-based PIB, and establish a clear relationship between the types/contents of oxygen functional groups and the regulated composition of SEI.

A high-performance and novel photocatalyst of BiVO4-reduced Graphene Oxide (BiVO4-rGO) nanocomposite was prepared by a facile hydrothermal method. The photocatalyst was characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electronic microscopy, UV-Vis diffusion reflectance spectroscopy, photoluminescence spectroscopy and UV-Vis adsorption spectroscopy, respectively. The visible-light photocatalytic activity was evaluated by oxidation of methyl orange (MO) under simulated sunlight irradiation. The results show that the BiVO4-rGO nanocomposites exhibit enhanced photocatalytic performance for the degradation of MO with a maximum removal rate of 98.95% under visible light irradiation as compared with pure BiVO4 (57.55%) due to the increased light absorption intensity and the degradation of electron-hole pair recombination in BiVO4 with the introduction of the rGO.

In this study, a bimetallic oxide catalyst of cobalt-manganese (CoMn2O4) was synthesized using the sol-gel method, and it was then characterized using a variety of techniques such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) spectroscopy, X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption-desorption isotherms. The obtained novel catalyst, i.e., CoMn2O4, was then used as an activator of peroxymonosulfate (PMS) for the catalytic degradation of a commonly-used UV filter, 2-phenylbenzimidazole-5-sulfonic acid (PBSA) in water. The effects of various factors (e.g., catalyst dosage, PMS concentration, reaction temperature, and pH) in the process were also evaluated. Chemical scavengers and electron paramagnetic resonance (EPR) tests showed that the •OH and SO4•- were the main reactive oxygen species. Furthermore, this study showed that CoMn2O4 is a promising catalyst for activating PMS to degrade the UV filters.

Antibiotics are increasingly detected in groundwater, but little is known about their presence in deep underground sediments. In this study, underground sediment samples were collected from pig farms, chicken houses, fishponds and riverbanks in a small region of the Jianghan Plain. Sixteen antibiotics were detected in different layers of sediments in various animal-breeding areas, with the riverbank containing the most pollution, followed by the fishpond, then the pig farm and the least being the chicken house. Samples taken from different sections of the collection sites and tested for each antibiotic compound revealed significant pollution, with the riverbank containing the most pollution, followed by the fishpond, then the pig farm and the least being the chicken house. The concentrations of the targets did not decrease with depth, but increased between 0.6 m and 1.0 m, which was a significant fluctuation. The aquifer sediment analysis indicated that the greatest antibiotic retention was within 8 m, with a small increase between 12 and 16 m, consistent with the depth of sandy aquifer layers. None of the compounds were detected in the deep layer at 20 m but for sulfadiazine and chlorotetracycline. Tetracyclines and Fluoroquinolones were the two groups observed at higher concentrations in most sediment layers, although their residual levels no more than 20 ng g-1. This study revealed that antibiotics generally exist in the underground environment, along with groundwater migration and particle adsorption. The pollution of antibiotics in alluvial sediments is an immense challenge to groundwater remediation, and its environmental effects should be studied.

Biocatalysis is increasingly becoming an alternative method for the synthesis of industrially relevant complex molecules. This can be realized by using enzyme immobilized polysaccharide-based 3D scaffolds as compatible carriers, with defined properties. Especially, immobilization of either single or multiple enzymes on a 3D printed polysaccharide scaffold, exhibiting well-organized interconnected porous structure and morphology, is a versatile approach to access the performance of industrially important enzymes. Here, we demonstrated the use of nanocellulose-based 3D porous scaffolds for the immobilization of glycosyltransferases, responsible for glycosylation in natural biosynthesis. The scaffolds were produced using an ink containing nanofibrillated cellulose (NFC), carboxymethyl cellulose (CMC), and citric acid. Direct-ink-writing 3D printing followed by freeze-drying and dehydrothermal treatment at elevated temperature resulted in chemically cross-linked scaffolds, featuring tunable negative charges (2.2-5.0 mmol/g), pore sizes (10-800 μm), fluid uptake capacity, and exceptional dimensional and mechanical stability in the wet state. The negatively charged scaffolds were applied to immobilize two sugar nucleotide-dependent glycosyltransferases (C-glycosyltransferase, Zbasic2-CGT; sucrose synthase, Zbasic2-SuSy), each harboring a cationic binding module (Zbasic2) to promote charge-based enzyme adsorption. Both enzymes were immobilized at ∼30 mg of protein/g of dry carrier (∼20% yield), independent of the scaffold used. Their specific activities were 0.50 U/mg (Zbasic2-CGT) and 0.19 U/mg (Zbasic2-SuSy), corresponding to an efficacy of 37 and 18%, respectively, compared to the soluble enzymes. The glycosyltransferases were coimmobilized and shown to be active in a cascade reaction to give the natural C-glycoside nothofagin from phloretin (1.0 mM; ∼95% conversion). All enzyme bound scaffolds showed reusability of a maximum of 5 consecutive reactions. These results suggest that the 3D printed and cross-linked NFC/CMC-based scaffolds could present a class of solid carriers for enzyme (co)-immobilization, with promising applications in glycosyltransferase-catalyzed synthesis and other fields of biocatalysis.