Synthesis of ternary geopolymers using prediction for effective solidification of mercury in tailings.

This study used steel slag, fly ash, and metakaolin as raw materials (SFM materials) to create silica-alumina-based geopolymers that can solidify Hg2+ when activated with sodium-based water glass. The experiments began with a triangular lattice point mixing design experiment, and the results were fitted, analyzed, and predicted. The optimum SFM material mass ratio was found to be 70% steel slag, 25% fly ash, and 5% metakaolin. The optimum modulus of the activator was identified by comparing the unconfined compressive strength and solidifying impact on Hg2+of geosynthetics with different modulus. The SFM geopolymer was then applied in the form of potting to cure the granulated mercury tailings. The inclusion of 50% SFM material generated a geosynthetic that reduced mercury transport to the surface soil by roughly 90%. The mercury concentration of herbaceous plant samples was also reduced by 78%. It indicates that the SFM material can effectively attenuate the migration transformation of mercury. Finally, characterization methods such as XPS and FTIR were used to investigate the mechanism of Hg2+ solidification by geopolymers generated by SFM materials. The possible solidification mechanisms were proposed as alkaline environment-induced mercury precipitation, chemical bonding s, surface adsorption of Hg2+ and its precipitates by the geopolymer, and physical encapsulation.

Modified phosphogypsum whiskers for decontamination of mercury tailings.

Mercury (Hg) tailings are hazardous solid wastes because of their high Hg concentrations. Modified phosphogypsum (PG) can decrease the bioactivity and mobility of heavy metals through chemisorption or electrostatic interactions. In this study, PG whiskers were modified by ZnCl2 and S, chitosan-hydrochloric acid, and thioglycolic materials; the resulting modified whiskers were used to decontaminate Hg tailings. Leaching tests and orthogonal experiments were conducted to optimize the modification parameters, including modifier quantity, pH, reaction temperature, and reaction time. The structure and physicochemical properties of the whiskers before and after modification were characterized through X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR). The stabilization efficiency of the modified PG whiskers ranged from 93.05 to 97.50%, demonstrating excellent stabilization effects. The stabilization was achieved through chemisorption or complexation. The decontamination process using modified whiskers reduced the pH and total nitrogen of the tailings; increased the cation exchange, total phosphorus, organic carbon, and total carbon; and made the tailings suitable for planting. In addition, the modified PG promoted the morphological transformation of Hg in the tailings, thereby significantly decreasing the Hg content in the effective states and mitigating the risk of Hg contamination.

Synthesizing sulfhydryl-functionalized biochar for effectively removing mercury ions from contaminated water.

Biochar is regarded as an effective adsorbent for heavy metal pollution treatment, and functional optimization is still needed to improve its performance. We created raw biochar (BC and BP) from corn straw and pine sawdust, which were modified to produce sulfhydryl-modified biochar (MBC and MBP). Isothermal adsorption experiments and adsorption kinetics experiments as well as the related model fitting were performed to evaluate the adsorption performance of biochar on Hg(II). According to the results of the Langmuir model fitting, the maximum adsorption capacities of sulfhydryl-modified biochar were 193.05 mg/g (MBC) and 178.04 mg/g (MBP), respectively, which were approximately 1.6 times higher than the raw biochar. The results showed that adding sulfhydryl groups to biochar can improve its adsorption performance. The prompt effect resulted from the sulfhydryl modification providing additional functional groups and enhanced chemisorption and physical adsorption properties.

Preparation of Ce x Zr1-x O2 by Different Methods and Its Catalytic Oxidation Activity for Diesel Soot.

Novel Ce x Zr1-x O2 (x = 0.67, 0.8, 0.9, 1.0) catalysts were designed and synthesized by solvothermal, calcination, and sol-gel methods and were used to catalyze oxidation of soot from diesel vehicle exhaust. The influence of catalysts synthesized by different methods and Ce/Zr molar ratios on the performance was investigated. These catalysts were characterized by XRD, N2 adsorption-desorption, FT-IR, TEM, XPS, H2-temperature programmed reduction (TPR), and O2-temperature programmed desorption (TPD) techniques. The results indicated that Ce0.8Zr0.2O2 prepared by the calcination method has excellent activity and stability at low temperature. The soot ignition point is 322 °C, and the ratio of soot conversion reaches 90% at 497 °C, which is lower than that from the solvothermal and sol-gel methods. The XRD, Raman, SEM, XPS and H2-TPR results reveal that the structure and oxygen adsorption properties are crucial to soot oxidation activity, and Zr4+ is successfully doped into the CeO2 lattice and forms a homogeneous solid solution. Nanostructured Ce0.8Zr0.2O2 with 110.2 m2/g surface areas is produced. The proportion of chemical oxygen and surface adsorbed oxygen in the catalyst prepared from the calcination method is the highest at 23.18%. The structure may lead to charge imbalance, unsaturated bonds, and oxygen vacancies, thus increasing the adsorption of oxygen on the catalyst surface.