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The mesoporous Cr/ZSM-5 and W-Cr/ZSM-5 zeolites have been successfully synthesized by loading chromium and tungsten on zeolite support. The metal loaded ZSM-5 catalysts were analyzed by several characterizations such as XRD, SEM-EDS, TEM, and BET. The catalytic activities and recycle efficiency were also investigated by applying catalysts for oxidation of oleic acid. These catalysts exhibited the high catalytic efficiency for cleavage of double bond with the use of H2O2. The oleic conversion of 88.7% and 93.3% could be achieved for Cr/ZSM-5 and W-Cr/ZSM-5 catalyst, respectively. Moreover, the modified ZSM-5 catalysts also demonstrated a long life time and high stability.

A note on versions:The version presented here may differ from the published version or from the version of record. If you wish to cite this item you are advised to consult the publisher's version. Please see the repository url above for details on accessing the published version and note that access may require a subscription.For more information, please contact eprints@nottingham.ac.uk AbstractThe surface-enhanced Raman (SER) signal of 4-aminothiolphenol (4-ATP) based on the surface of gold nanoparticles colloids with size distributed from 2 to 5 nm were used as labeling agent to detect basal cell carcinoma (BCC) of skin. The enhanced Raman band at 1075 cm -1 corresponding to C-S stretching vibration in 4-ATP was observed during attachement to the surface of gold nanoparticles. The frequency and intensity of this band did not change when the colloids were conjugated with BerEP4 antibody which specifically binds to BCC. We show the feasibility of imaging BCC by SERS scanning the 1075 cm -1 band to detect the distribution of 4-ATP-attached gold nanoparticles attached to skin tissue ex-vivo.

This article provides a comprehensive assessment of dioxins contaminating the soil and evaluates the bioremediation technology currently being widely used, and also offers recommendations for future prospects. Soil pollution containing dioxins is extremely toxic and hazardous to human health and the environment. Dioxin concentrations in soils around the world are caused by a variety of sources and outcomes, but the main sources are from the consequences of war and human activities. Bioremediation technology (bioaugmentation, biostimulation, and phytoremediation) is considered an optimal and environmentally friendly technology, with the goal of applying native microbial communities and using plant species with a high biomass to treat contaminated dioxins in soil. The powerful bioremediation system is the growth of microorganisms that contribute to the increased mutualistic and competitive relationships between different strains of microorganisms. Although biological treatment technology can thoroughly treat contaminated dioxins in soil with high efficiency, the amount of gas generated and Cl radicals dispersed after the treatment process remains high. Further research on the subject is required to provide stricter control over the outputs noted in this study.

Activated carbon has been used to treat organic dyes in water systems; however, the adsorption capacity of the samples studied was limited by the specific surface area and influenced by the pH of the aqueous solution. In this study, a hybrid adsorbent consisting of a mixture (MCS) of activated chestnut shell biochar (CN) and pyrolyzed snail shell material (SS) was developed to solve this problem, with the waste snail shell samples being processed by pyrolysis and the chestnut shell samples chemically pretreated and then pyrolyzed. The BET and SEM results revealed that the SS had a mesoporous fluffy structure with a higher specific surface (1705 m2/g) and an average pore diameter of about 4.07 nm, providing a large number of sites for adsorption. In addition, XPS and FTIR results showed that the main component of SS was calcium oxide, and it also contained a certain amount of calcium carbonate, which not only provided an alkaline environment for the adsorption of biochar but also degradation and photocatalytic capabilities. The results showed that the MCS3-1 sample, obtained when CN and SS were mixed in the ratio of 3:1, had good capacity for adsorption for methylene blue (MB), with 1145 mg/g at an initial concentration of 1300 mg/L (92% removal rate). The adsorption behaviors were fitted with the pseudo-second-order kinetic model and Freundlich isotherm model, which indicated that the adsorption was multilayer chemisorption with a saturated adsorption capacity of 1635 mg/g. The photocatalytic capacity from the SS composition was about 89 mg/g, and the sorption of MB dye onto the sorbent reached equilibrium after 300 min. The results suggested that MCS3-1 has enormous potential for removing MB from wastewater.

While enjoying the convenience of nuclear energy development, the environmental contamination by radionuclide leakage is of significant concern. Because of its cost-effectiveness and environmental friendliness, biochar has attracted a lot of attention in the field of radioactive water treatment. Herein, a novel teak peel modified biochar (labeled as PMBN3) was prepared and applied to remove strontium from artificial seawater. The characterisation of the prepared PMBN3 showed it contains numerous oxygen-containing functional groups (i.e. carboxyl and hydroxyl groups), laminar morphology, mesoporous structure, large specific surface area. PMBN3 exhibited great advantages in Sr(II) adsorption, such as rapid adsorption kinetics (<1 h for equilibrium) and superior reusability. The adsorption of strontium by biochar is consistent with pseudo-second order and internal diffusion kinetic models. Among the four types of adsorption isotherms, the Freundlich isotherm showed the best fit with R2 > 0.98. The calculated thermodynamic parameters indicate that strontium adsorption on biochar occurs exothermically and spontaneously. Furthermore, for efficient removal of Sr(II), CO2 nanobubbles were blown into artificial seawater to precipitate the interfering metal ions, and followed by the adsorption of PMBN3 towards residual metal ions with the removal rate of Sr(II) over 99.7%. Finally, mechanistic studies have shown that the strontium adsorption process by PMBN3 is a multiple adsorption mechanism consisting of ion exchange between H+ (from -OH and -COOH) and Sr(II), and weak intermolecular forces between Sr(II) and the PMBN3 adsorbent. This study creatively combines chemisorption and nanobubble precipitation for strontium removal, which provides great reference value and guidance for environmental remediation.