A cancer cell nanotherapy method based on GHz film bulk acoustic resonator and nanoscale CaO2.

Sonodynamic therapy (SDT) is an emerging cancer treatment method in recent years. However, the ultrasound signal utilized for SDT is usually located at a low-frequency spectrum (<2 MHz), and in the field of SDT research, few studies have focused on the exploration and development of ultrasound frequency. Studies have shown that the GHz-level ultrasound can increase cell membrane permeability and have a negligible effect on cell vitality. Herein, we reported the study of a GHz thin film bulk acoustic resonator as an ultrasound source for synergistic treatment with nanoscale calcium peroxide (CaO2). It was discovered that this ultrasound source ultimately achieved an efficient therapeutic outcome on mouse breast cancer cell line 4T1. Such GHz-level ultrasound application in SDT is of high significance to broaden the cognition and application scope of SDT.

Different effects of selenium speciation on selenium absorption, selenium transformation and cadmium antagonism in garlic.

Currently, planting selenium-rich crops using inorganic selenium such as selenate and selenite is used to address human selenium deficiency problems. In this paper, besides the above two traditional inorganic selenium speciation, we chose a new organic selenium speciation of potassium selenocyanoacetate to investigate the different effects of selenium speciation on selenium absorption, selenium transformation and cadmium antagonism via foliar application. Plantingexperiments showed that the selenium content of garlic bulbs treated with organic selenium was 1.8-3.9 times higher than that of inorganic selenium. Additionally, the absorption and transformation efficiency of organic selenium in garlic was also the highest, reaching over 95 %. Importantly, it was noteworthy that the cadmium content in bulbs treated with organic selenium was significantly lower than the Chinese food safety standard (0.2 mg/kg). Hence, this study provides an efficient organic selenium speciation which is beneficial to meet human selenium requirements and ensure safe utilization of cadmium-contaminated soils.

Colloidal iron species driven enhanced H2O2 decomposition into hydroxyl radicals for efficient removal of methylene blue from water.

Colloids are wide-spread in natural waters and colloid-facilitated transport via adsorption was established as the most important mechanism for the mobilization of aqueous contaminants. This study reports another possible, but reasonable, role of colloids for the contaminants driven by redox reactions. Under the same conditions (pH 6.0, 0.3 ml 30% H2O2, and 25 °C), the degradation efficiencies of methylene blue (MB) at 240 min over Fe colloid, Fe ion, Fe oxide and Fe(OH)3 were 95.38%, 42.66%, 4.42% and 9.40%. We suggested that, Fe colloid can promote the H2O2 based in-situ chemical oxidation process (ISCO) compared with other iron species such as Fe(Ⅲ) ion, Fe oxide and Fe(OH)3 in natural water. Furthermore, the MB removal via adsorption by Fe colloid was only 1.74% at 240 min. Hence, the occurrence, behavior and fate of MB in Fe colloid containing natural water system mainly depends on the reduction-oxidation rather than adsorption-desorption process. Based on the mass balance of colloidal iron species and characterization of iron configurations distribution, Fe oligomers were the active and dominant components for Fe colloid-driven enhanced H2O2 activation among three types of Fe species. The quick and steady conversion of Fe(III) to Fe(II) was proven to be reason why Fe colloid can efficiently react with H2O2 to produce hydroxyl radicals.

Film-based fluorescent sensor for visual monitoring and efficient removal of aniline in solutions and gas phase.

Aniline has attracted much concern for its long degradation half-life and huge toxicity to the environment and human beings. Therefore, the development of a multi-functional device for visual detection and efficient removal of aniline was highly anticipated. In our work, the small-size Eu@UiO-66(COOH) was obtained by post-synthesis modification (PSM), and then the film-based fluorescent sensor was prepared by crosslinking reaction. The films not only showed incredible mechanical stability and potential for large-scale preparation, but also have excellent fluorescence response to aniline in solutions and gas phase. As the concentration of aniline increased, the fluorescence of films gradually increased at 350 nm, while the fluorescence gradually quenching at 620 nm, and the detection limits (LOD) of aniline in water and air were 0.27 ppb and 0.086 ppb, respectively. In addition, the adsorption performance of the film for aniline has also been confirmed and the maximum adsorption capacity was 32.6 mg/g, which is a strong guarantee for the realization of ultra-trace detection and toxicity reduction of aniline. In summary, the multi-functional film sensor has been designed for ultra-trace detection and efficient removal of aniline in solutions and gas phase, and have significant value for pollutant treatment, ecological restoration and early prevention.

New Insight into a Fenton-like Reaction Mechanism over Sulfidated ß-FeOOH: Key Role of Sulfidation in Efficient Iron(III) Reduction and Sulfate Radical Generation.

Sulfidation can greatly improve the efficiency of utilization of reducing equivalents for contaminant removal; however, whether this method benefits Fenton-like reactions or not and the possible mechanism are not well understood. In this study, we revealed that surface sulfidation can greatly promote the heterogeneous Fenton activity of ß-FeOOH (Fe3S4@ß-FeOOH) by 40 times, in which not only the •OH formation was enhanced but also SO4•- as a new oxidation species was generated. Moreover, their contribution to metronidazole (MTZ) degradation was 52.5 and 37.1%, respectively. In comparison, almost no HO2•/O2•- was detected in the Fe3S4@ß-FeOOH/H2O2 system. These results were different from some previously reported Fenton counterparts. Based on the characterization and probe experiments, sulfur species, including S2-, S0, and Sn2-, as an electron donor and electron shuttle were responsible for efficient conversion of Fe(III) into Fe(II) other than via the Haber-Weiss mechanism, leading to excellent •OH generation via a Fenton-like mechanism. Most importantly, HSO5- can be generated from SO32- oxidized by •OH, and its scission into SO4•- was not dependent on the extra electric potential or Fe-O2-S(IV) intermediate. These findings provided new insight for utilizing sulfidation to improve the activity of iron-based Fenton catalysts.

Hydroxyl Radical-Involving p-Nitrophenol Oxidation during Its Reduction by Nanoscale Sulfidated Zerovalent Iron under Anaerobic Conditions.

Sulfidated zerovalent iron (S-ZVI) has been extensively used for reducing pollutants. In this study, the oxidation process in the reductive removal of p-nitrophenol (PNP) by S-ZVI was confirmed under anaerobic conditions. We revealed that a PNP oxidation process involving •OH resulted from the H2O2 activation by surface-bound Fe(II) in S-ZVI, in which H2O2 was generated via a surface-mediated reaction between water and FeS2. Only the PNP reduction process occurred for ZVI. Herein, efficient PNP degradation by S-ZVI resulted from two functions: reduction into p-aminophenol due to enhanced electron transfer and PNP oxidation into p-benzoquinone by •OH radicals from the interaction of surface-bound Fe(II) and in situ generated H2O2, the contributions of the oxidation and reduction processes to PNP degradation over S-ZVI were 10 and 90%, respectively. Sulfur in S-ZVI suppressed the pH increase in the reaction media and produced more surface-bound Fe(II) than ZVI for •OH generation via the heterogeneous Fenton reaction process. Since different degradation pathways could lead to different effects on the water environment, such as toxicity, our findings suggest that the oxidizing process induced by S-ZVI during groundwater decontamination should be considered.

A versatile logic detector and fluorescent film based on Eu-based MOF for swift detection of formaldehyde in solutions and gas phase.

Due to the huge threat of formaldehyde (FA) on human beings, the development of chemical sensors for swift detection of FA in solutions and gas phase is highly anticipated. In this paper, a versatile logic detector and a portable fluorescent film based on small-scaled Eu-based MOF were applied successfully to detect FA in solutions and gas phase, respectively. For FA in aqueous solution, the design of logic detector will efficiently identify FA in different concentration ranges: when the FA concentration are 0-500 ppb, 500-1000 ppb and >1000 ppb, the output signals of logic detector are the concentration level of FA ("L", "H" and "VH"), and accompanied by red, purple and blue signal lamps to remind, respectively. For FA in the air, the color of rigid film sensor will gradually change from red to blue with the increase of FA under UV lamp, and the detection limit of gaseous FA is 11.8 ppb. Through the preparation of logic devices and fluorescent films, Eu-based MOF realized swift detection of FA in solutions and gas phase, which will be very helpful to improve the human response level to FA from different emission sources.

Fe3O4@S-doped ZnO: A magnetic, recoverable, and reusable Fenton-like catalyst for efficient degradation of ofloxacin under alkaline conditions.

In this study, an efficient and reusable heterogeneous Fenton catalyst Fe3O4@S-doped ZnO magnetic composite was synthesized for the degradation of ofloxacin (OFX) under alkaline conditions without external energy input. The Fe3O4@S-doped ZnO exhibited excellent catalytic activity toward ofloxacin degradation within 120 min. Using 0.25 g/L of catalyst and 5.0 mL/L of H2O2 under optimized conditions, the catalyst was effective in pH values ranging from 5.2 to 9.0. The catalytic performance at optimal conditions was in accordance with a pseudo-first-order kinetics model. The reaction constant of Fe3O4@S-doped ZnO (0.0354 min-1) was three times than that of Fe3O4@ZnO (0.0124 min-1) under alkaline conditions (pH 8.2). The reactive oxygen species were the ·OH and O2·-, with ·OH dominating in the degradation of OFX. It is proposed that the catalyst acts as a Lewis acid, creating an acidic microenvironment on the catalyst's surface and widening the pH range of the Fenton reaction to alkaline conditions. Additionally, the catalyst was stable and reusable after six cycles of use. The Fenton-like Fe3O4@S-doped ZnO catalyst overcomes the problem of the narrow pH of the reaction system, thus providing promising environmental applications.

Degradation characteristics of humic acid over iron oxides/Fe 0 core-shell nanoparticles with UVA/H2O2.

Iron oxides coated on Fe(0) core-shell nanospheres (nIOCI) were synthesized through the reduction of ferrous sulfate aqueous solution by sodium borohydride at ambient atmosphere. The catalyst was highly effective for the degradation of humic acid (HA) in the presence of H(2)O(2) and UVA at neutral pH. Under deoxygenated conditions in the dark, the generation of hydroxyl radicals in aqueous nIOCI dispersion verified its galvanic cell-like performance, which enhanced the interfacial electron transfer and led to its higher reactivity. By the total organic carbon, the absorbance of UV(254), FTIR, the molecular weight distribution and the chemical fractional character analysis, the degradation process of HA was shown to proceed by the disappearance of aromaticity, the increase of hydrophilic fraction and aromatic ring openings into CO(2) and small organic acid. The treated HA showed much lower reactivity toward chlorine and the disinfection byproduct (DBP) formation potential was also greatly reduced. Moreover, it was found that the DBP formation potential more depended on the structure of the intermediates of HA degradation than TOC removal.