Effect of phosphogypsum on saline-alkalinity and aggregate stability of bauxite residue

A column experiment was conducted to investigate the effect of phosphogypsum (PG) on the saline- alkalinity, and aggregate stability of bauxite residue. Results showed that: with increasing leaching time, the concentrations of saline-alkali ions decreased while the concentration increased in bauxite residue leachate; compared with CK (control group) treatment, pH, electric conductivity (EC), exchangeable sodium percentage (ESP), sodium absorption ratio (SAR), and exchangeable Na⁺ content of bauxite residue were reduced following PG treatment; average particle sizes in aggregates following CK and PG treatments were determined to be 155 and 193 nm, respectively. SR-μCT test results also confirmed that bauxite residue following PG treatment acquired larger aggregates and larger pore diameter. These results indicate that the PG treatment could significantly modulate the saline-alkalinity, and simultaneously enhance aggregate stability of bauxite residue, which provides a facile approach to reclaim bauxite residue disposal areas.     

Rapid preparation of Palygorskite/Al2O3 composite aerogels with superhydrophobicity,high-temperature thermal insulation and improved mechanical properties

Al₂O₃ aerogels are widely employed in heat insulation and flame retardancy because of their unique combination of low thermal conductivity and exceptional high-temperature stability. However, the mechanical properties of Al₂O₃ aerogel are poor, and the preparation time is considerably long. In this study, we present a simple and scalable approach to construct monolithic Pal/Al₂O₃ composite aerogels using solvothermal treatment instead of traditional solvent replacement, which remarkably shortened the preparation time. Subsequently, to obtain stable superhydrophobicity (θ > 152°), the Pal/Al₂O₃ aerogel was modified by gas-phase modification method. The obtained Pal/Al₂O₃ composite aerogels demonstrate the integrated properties of low density (0.078–0.106 g/cm³), low thermal conductivity (1000 °C, 0.143 W/(m·K)), good mechanical properties (Young's modulus, 1.6 MPa), and good heat resistance. The monolithic Pal/Al₂O₃ composite aerogels with improved mechanical performance and improved thermal stability can show great potential in the field of thermal insulation.     

A zirconium-free glaze system for sanitary ceramics with SiO2-CaCO3-TiO2 composite opacifier containing anatase: Effect of interface combination among SiO2, CaCO3 and TiO2

TiO₂ is an ideal substitute to ZrSiO₄ ceramic opacifier, yet it is limited to application because of the undesirable yellowing resulting from rutile formation. Herein, the SiO₂-CaCO₃-TiO₂ composite opacifier (Si-Ca-Ti) was constructed. The glaze used Si-Ca-Ti presents a superior opacification performance than ZrSiO₄ opacified glaze without causing yellowing, showing L*, a*, b* values of 94.81, -0.67 and 3.23. By comparison, the glaze using SiO₂, CaCO₃, and TiO₂ mixture shows lower opacification and yellowish surface with L* and b* values of 92.99 and 5.36. It is revealed that there is a close interface bonding among SiO₂, CaCO₃ and TiO₂ in Si-Ca-Ti, which promotes their combination reaction to generate opacification phase titanite and inhibit rutile formation when sintering, resulting in the white surface and opacification improvement of the glaze. This study proposes a green and efficient strategy to achieve white and highly opacified glaze for sanitary ceramics, exhibiting good application prospect.     

纳米零价铁材料对放射性核素的 去除及机理研究进展

随着人类社会的发展，放射性铀矿的开采和使用越来越多，环境面临着越来越严重的放射性污染问题。从生物和环境的角度来看，有效地清除环境中的放射性核素是核能利用过程中最重要的问题之一。纳米零价铁（nanoscale zero valent iron, nZVI）具有较大的比表面积和较高的活性位点，能显著提高放射性污染物的修复效率。本综述的目的是展示nZVI基材料对放射性核素的高效去除能力和环境修复作用。简介了常用的nZVI基材料（表面改性或多孔材料支撑的nZVI材料）及其对放射性核素的去除效果和相互作用机制（如吸附和氧化还原）。最后，对nZVI材料的应用和挑战给出个人见解。本综述有助于为高效去除放射性核素的nZVI材料的设计指明方向，为放射性核素的高效处理处置提供新材料。     

Novel nanorod Ti0·7Ir0·3O2 prepared by facile hydrothermal process: A promising non-carbon support for Pt in PEMFCs

Late transition metal doped TiO₂ has been exploited for generating efficient catalyst support by enhancing electrical conductivity and modifying properties of TiO₂. The Ti_0·7Ir_0·3O₂ nanorod (NRs), a novel catalyst support for Pt nanoparticles, was prepared for the first time via single-step hydrothermal process at low temperature using IrCl₃·3H₂O and TiCl₄ as starting materials. We found that the Ti_0·7Ir_0·3O₂ NRs with 70–80 nm in length and 25–30 nm in width is successful prepared at 210 °C for 12 h without utilizing surfactants or stabilizers. In addition, the Ti_0·7Ir_0·3O₂ NRs was presented principally as a single-phase solid with the TiO₂ is in the rutile form with high crystallinity without using further treatment after synthesis. More importantly, we found that the Ti_0·7Ir_0·3O₂ NRs possesses high electrical conductivity (0.028 S cm⁻¹) dealing the intrinsically non-conducted drawback of TiO₂. The Pt nanoparticles were then deposited on the support of Ti_0·7Ir_0·3O₂ NRs via chemical reduction method. The properties of 20 wt % Pt/Ti_0·7Ir_0·3O₂ NRs electrocatalyst were characterized by X-ray diffraction (XRD), Transmission electron microscopy (TEM), the cyclic voltammetry (CV). The uniformly distributed small Pt nanoparticles (3–4 nm diameter) were well adhered to the Ti_0·7Ir_0·3O₂ NRs. The electrochemically active surface area (ECSA) of 20 wt % Pt/Ti_0·7Ir_0·3O₂ NRs was higher than that of the commercial 20 wt % Pt/C (E-TEK) due to the small size and good dispersion of Pt nanoparticles on the surface of Ti_0·7Ir_0·3O₂ NRs. Moreover, the ECSA value of the Pt/Ti_0·7Ir_0·3O₂ NRs retained up to 88% after 2000 cycles of cyclic voltammetry, suggesting the high stability of catalyst resulted from strong metal support interaction (SMSI) of Titania-based materials with the noble metals. More importantly, the onset potential of Pt/Ti_0·7Ir_0·3O₂ NRs catalyst towards oxygen reduction reaction is more positive (∼80 mV) compared to commercial Pt/C, indicating the high catalytic activity of the Pt/Ti_0·7Ir_0·3O₂ NRs catalyst. The results of this research suggested that novel Ti_0·7Ir_0·3O₂ NRs could be applied as promising robust non-carbon support for Pt. This research also creates a preliminary step for investigating systematically promising Iridium doped Titania materials.     

ZnIn2S4/In(OH)3 hollow microspheres fabricated by one-step l-cysteine-mediated hydrothermal growth for enhanced hydrogen production and MB degradation

An intervening barrier for photocatalytic water decomposition and pollutant degradation is the frustratingly quick recombination of e⁻ - h⁺ pairs. Delicate design of heterojunction photocatalysts by coupling the semiconductors at nanoscale with well-matched geometrical and electronic alignments is an effective strategy to ameliorate the charge separation. Here a facile and environment-friendly l-cysteine-assisted hydrothermal process under weakly alkaline conditions is demonstrated for the first time to fabricate ZnIn₂S₄/In(OH)₃ hollow microspheres with intimate contact, which are verified by XRD, SEM, (HR)TEM, XPS, N₂ adsorption-desorption, UV–Vis DRS and photoluminescence spectra. ZnIn₂S₄/In(OH)₃ heterostructure (L-cys/Zn²⁺ = 4, molar ratio) with a band-gap of 2.50 eV, demonstrates the best photocatalytic performance for water reduction and MB degradation under visible light, outperforming its counterparts (In(OH)₃ and ZnIn₂S₄). The excellent activity of ZnIn₂S₄/In(OH)₃ heterostructure arises from the intercrossed band-edge positions as well as the unique hollow structure with large surface area and wide pore-size distribution, which are beneficial for the efficient charge migration from bulk to surface as well as at the interface between ZnIn₂S₄ and In(OH)₃. This work provides an efficient and eco-friendly strategy for one-pot synthesis of heterostructured composites with intimate contact for photocatalytic application.     

Effects of WO3 doping on stability and N2O escape of MnOx–CeO2 mixed oxides as a low-temperature SCR catalyst

MnO_x–WO_x–CeO₂ catalysts synthesized using a sol–gel method were investigated for the low-temperature NH₃-SCR reaction. Among them, W_0.1Mn_0.4Ce_0.5 mixed oxides exhibited above 80% NO_x conversion from 140 to 300 °C. In addition, this catalyst exhibited high stability and CO₂ tolerance in a 50 h activity test at 150 °C. Substantially reduced N₂O production and enhanced N₂ selectivity were achieved by WO₃ doping, which was due to the weakened reducibility and increased number of acid sites. The decreased SO₂ oxidation activity as well as the reduced formation of ammonium and manganese sulfates resulted in a high SO₂ resistance of this catalyst.