Given the serious harm of toxic phenol to human health and the ecological environment, it is urgent to develop an efficient, low-cost and sensitive nanoenzyme-based method to monitor phenol. MOF-derived nanozyme has attracted wide interest due to its hollow polyhedra structure and porous micro-nano frameworks. However, it is still a great challenge to synthesize MOF-derived multimetal synergistic catalytic nanoenzymes in large quantities with low cost. Herein, we reported the synthetic strategy of porous hollow CA-CoNiMn-CLDHs with ZIF-67 as templates through a facile solvothermal reaction. The prepared trimetallic catalyst exhibits excellent peroxidase-like activity to trigger the oxidative coupling reaction of 4-AAP and phenol in the presence of H2O2. The visual detection platform for phenol based on CA-CoNiMn-CLDHs is constructed, and satisfactory results are obtained. The Km value for CA-CoNiMn-CLDHs (0.21 mM) is lower than that of HRP (0.43 mM) with TMB as the chromogenic substrate. Because of the synergistic effect of peroxidase-like activity and citric acid functionalization, the built colorimetric sensor displayed a good linear response to phenol from 1 to 100 μM with a detection limit of 0.163 μM (3σ/slope). Additionally, the CA-CoNiMn-CLDHs-based visual detection platform possesses high-chemical stability and excellent reusability, which can greatly improve economic benefits in practical applications.
The preparation of glass–ceramics with red mud and steel slag can not only solve the pollution problem caused by industrial waste slag but also produce economic benefits. It is difficult to analyze the high-temperature melt with the existing test methods, so the simulation experiment with molecular dynamics calculation becomes an important research method. The effects of steel slag content on the microstructure of red mud glass–ceramics were studied by molecular dynamics method. The results show that the binding ability of Si-O, Al-O, and Fe-O decreases with the increase in steel slag content. The number of Si-O-Si bridge oxygen increased gradually, while the number of Al-O-Al, Al-O-Fe, and Fe-O-Fe bridge oxygen decreased significantly. The number of tetrahedrons [SiO4] increased, the number of tetrahedrons [FeO4] and [AlO4] decreased, and the total number of three tetrahedrons decreased. The mean square displacement value of Si4+ and O2− increases first and then decreases, resulting in the viscosity of the system decreasing first and then increasing. The molecular dynamics method is used to analyze the structure of red mud–steel slag glass–ceramics on the microscopic scale, which can better understand the role of steel slag and has guiding significance for the experiment of this kind of glass–ceramics.
Ca2Si was successfully synthesized via a high-temperature melting furnace and a spark plasma sintering process, allowing its thermoelectric properties to be studied. High-temperature melting furnaces were utilized to inhibit the volatilization of Ca elements during the preparation stage, ensuring the production of high-purity Ca2Si. The resistivity of Ca2Si increased gradually with rising temperature and reached 12 mΩ·cm at 873 K, demonstrating semi-metallic characteristics. In the temperature range of 323 K–873 K, Ca2Si displayed relatively low total thermal conductivity, from 1.1 to 1.7 W·m−1·K−1. Nevertheless, Ca2Si attained a maximum thermoelectric figure of merit (ZT) of 0.1 due to the atypical behavior and electrical properties of semiconductors. In contrast, Mg2Si achieved a ZT value of 0.32 at 873 K, owing to its exceptional Seebeck coefficient.
Microbially influenced corrosion (MIC) in anaerobic environments accounts for many severe failures and losses in different industries. Sulfate-reducing bacteria (SRB) represent a typical class of corrosive microorganisms capable of acquiring electrons from steel through extracellular electron transfer processes, thereby inducing severe electrical microbially influenced corrosion (EMIC). Although prior research has underscored the significance of extracellular electron transfer, the contribution of EMIC to the whole MIC has not been comprehensively studied. In this study, Q235 steel coupons were employed in an H-shaped electrochemical cell to conduct electrochemical and coupon immersion experiments, aiming to determine the contribution of EMIC to the overall MIC. The experiments were conducted under two distinct carbon source conditions: 100% carbon source (CS) and 1% CS environments. It was observed that the biotic electrodes exhibited significantly higher cathodic currents, with the most pronounced biological cathodic activity detected in the 100% CS biotic medium. The voltammetric responses of the electrodes before and after changes in the medium confirmed the biocatalytic capability of the attached biofilm in stimulating the cathodic reaction. The proportion of EMIC in MIC was calculated using linear polarization resistance, revealing a trend over time. Additionally, weight loss tests indicated that the contribution of EMIC to the total MIC was approximately 27.69%. Furthermore, the results demonstrated that while the overall corrosion rate was lower in the 1% CS environment, the proportion of EMIC in MIC increased to approximately 37.68%.