Search

Herein, orderly arranged bamboo-like mesoporous silica materials were prepared using cetyltrimethylammonium bromide (CTAB) as the template and n-hexanol as the long-chain alcohol cosurfactant. The ordered meso-structure was characterized by XRD analysis, field emission scanning electron microscopy (FE-SEM, Hitachi S4800), transmission electron microscopy, BET and IR spectroscopy analysis. The effects of the CTAB/n-hexanol molar ratio(R), length of the hydrophobic chain with a terminating hydroxyl group on the long-chain alcohol cosurfactant, parity of the hydrophobic carbon atoms on the surface topography, specific surface area, and pore size of the powder were investigated. The results showed that when the molar ratio = 1, the mesoporous silica presented neatly arranged bamboo segment lengths of 19.6–23.9 μm, platycodon grandiflorum widths of 2.13–3.32 μm, pore size of 3.04 nm, and surface area of 820.034 m2/g. Increasing or decreasing the amount of n-hexanol directing led to denser or looser lateral molecular interactions between CTAB and the co-structure-directing agents that respectively reduced or increased the pore size, with the latter resulting in the formation of spherical particles. When n-hexanol was replaced by n-heptanol or n-octanol, the pore size and surface area of the mesoporous silica decreased significantly with the increase in the hydrophobic chain length. [ABSTRACT FROM AUTHOR]

Laccase immobilized and cross-linked on Fe3S4/earthworm-like mesoporous SiO2 (Fe3S4/EW-mSiO2) was used to degrade methoxychlor (MXC) in aqueous environments. The effects of various parameters on the degradation of MXC were determined using free and immobilized laccase. Immobilization improved the thermal stability and reuse of laccase significantly. Under the conditions of pH 4.5, temperature 40 °C, and reaction time 8 h, the degradation rate of MXC by immobilized laccase reached a maximum value of 40.99% and remained at 1/3 of the original after six cycles. The excellent degradation performance of Fe3S4/EW-mSiO2 was attributable to the pyrite (FeS2) impurity in Fe3S4, which could act as an electron donor in reductive dehalogenation. Sulfide groups and Fe2+ reduced the activation energy of the system resulting in pyrite-assisted degradation of MXC. The degradation mechanism of MXC in aqueous environments by laccase immobilized on Fe3S4/EW-mSiO2 was determined via mass spectroscopy of the degradation products. This study is a new attempt to use pyrite to support immobilized laccase degradation. [ABSTRACT FROM AUTHOR]

The "trinitrogen" [ammonia nitrogen (NH4+ − N), nitrate nitrogen (NO3− − N), and nitrite nitrogen (NO2− − N)] from industrial or domestic wastewater can lead to eutrophication of water bodies. When ammonia nitrogen is converted into nitrate nitrogen, it will cause high nitrogen oxygen demand, which will also lead to hyperammonemia. High nitrite content in water bodies will increase the risk of human cancer. In this paper, Fe-Ce bimetallic-doped composites (Fe-Ce/SiO2 and Fe-Ce-SiO2/TiO2) were synthesized using SiO2 aerogel as a carrier for the adsorption and degradation of "three nitrogen." SiO2/TiO2 was prepared by dipping method, and Fe and Ce bimetals were loaded on the surface of SiO2/TiO2 material, and the effect of photo-Fenton oxidation on the degradation rate of three nitrogen under different materials was explored. The results showed that when the dosage of catalyst was 0.01 g, pH value was 11.0, and the concentration of H2O2 was 80 mmol/L, the photocatalytic efficiency was the best, and the degradation efficiency of three nitrogen remained above 70%. [ABSTRACT FROM AUTHOR]