Adsorption of acetone, ethyl acetate and toluene by beta zeolite/diatomite composites: preparation, characterization and adsorbability.

The hierarchical porous composites (Beta/Dt) were prepared by secondary growth method using natural diatomite and beta zeolite. Moreover, XRD, SEM, and BET characterize the composite's composition, surface structure, and pore structure. The adsorbability of Beta/Dt was evaluated by adsorption of three common volatile organic compounds (VOCs) of the printing industry: acetone, ethyl acetate, and toluene. The results show that under the optimum preparation condition, the adsorption capacities of the three VOCs on Beta/Dt were about 3.5 times those of pure beta zeolite and 4.7-35.3 times those of diatomite, respectively. It indicates the synergistic adsorption effect between beta zeolite and diatomite. The superior adsorption capacity of Beta/Dt can be attributed to the suitable micropore size, the increase of the diffusion channels, and the chemical adsorption on modification diatomite. The adsorption of acetone, ethyl acetate, and toluene on Beta/Dt conformed to the pseudo-second-order kinetic model. In contrast, adsorption isotherms conformed to the Langmuir model, meaning that both physical and chemical adsorption occurred simultaneously during the adsorption process, and the adsorption belonged to the monolayer adsorption. The chemical adsorption mechanism can be ascribed to the nucleophilic reaction between the three VOCs (acetone, ethyl acetate, and toluene) and Beta/Dt with positive charges resulting from the modification diatomite. Furthermore, the composite could still keep more than 90% of the adsorption capacity of the original adsorbent after five regeneration cycles.

Removal of tetracyclines from aqueous solutions by electrocoagulation/pecan nutshell coupling processes: synergistic effect and mechanism.

The present work compared electrocoagulation (EC)/pecan shell (PS) coupling process with a simple electrocoagulation (EC) process for the removal of tetracyclines (TCs). The results indicated that the addition of appropriate PS could lead to the enhancement of the removal efficiency and decrease of operating time via synergistic influence, including conventional EC process, biomass materials adsorption, charge neutralization and coordination adsorption. The ideal condition for the coupling process was 2.5 mA/cm2 for current density and 3 cm for plate spacing. Based on the optimum condition, when the dosage of PS was 5 g/L, the initial concentration of tetracycline hydrochloride (TC), oxytetracycline hydrochloride (OTC) and chlortetracycline hydrochloride (CTC) was 250 mg/L, the removal rate of PS was 55.90%, 45.10% and 14.98% higher than those of EC process after 40 min treatment. In addition, compared to conventional EC process, the unit energy demand (UED) decreased by 49.62%, 53.2 4% and 26.35% and the unit electrode material demand (UEMD) decreased by 49.80%, 85.65% and 44.37%, respectively, which means more energy conservation and environmental protection.

Effects of oxalic acid on Cr(VI) reduction by phenols in ice.

Since Cr(VI) is highly toxic, the environmental reduction of Cr(VI) to Cr(III) has attracted significant attention. Oxalic acid, a primary component of dissolved organic matter (DOM), is widely distributed throughout the natural environment but the reduction of Cr(VI) by oxalic acid is insignificant at the low concentrations present in the environment; however, the reduction of Cr(VI) is accelerated significantly in ice. In terms of combined pollution, Cr(VI) can coexist with other organic pollutants in the environment but the impact of organic pollutants on the reduction of Cr(VI), changes to the organic pollutants themselves, and the role of oxalic acid in these reactions are unknown. In this study, we investigated redox reactions between Cr(VI) and phenolic compounds in ice (- 15 °C) in the presence of oxalic acid and compared these to room temperature redox reactions in aqueous solutions (20 °C). While these redox reactions were negligible in aqueous solution, they were significantly accelerated in ice under acidic conditions, which was primarily attributed to the freeze concentration effect. Oxalic acid has two functions in these redox reactions; the first is to provide the H+ required for the reaction and the second is to serve as a reducing agent. When oxalic acid and phenolic pollutants coexist, Cr(VI) preferentially reacts with the phenolic compounds. Phenol, 4-chlorophenol (4-CP), and 2,4-dichlorophenol (2,4-DCP) were each demonstrated to reduce Cr(VI) in ice, but the reaction rate and overall reactivity of these three phenolic compounds are different.

Comparison of the photoconversion of 1-chloronaphthalene and 2,3-dichlornaphthalene in water.

In this work, the photoconversion of 1-chloronaphthalene (CN-1) and 2,3-dichlornaphthalene (CN-10) under the simulated sunlight had been studied. The results showed that the photoconversion of CN-1 and CN-10 obeyed the first-order kinetics model. NO2 -, NO3 -, Fe3+ and Fe2+ extensively present in natural water can accelerate CN-1 photoconversion via generating ·OH, which may induce indirect photooxidation of CN-1. The photoproducts were treated by the derivatization method and analyzed by GC-MS after being irradiated for 6 h. Ten products were characterized for CN-1 and CN-10, and there were six common products. On this basis, the photoconversion pathways of CN-10 and CN-1 were proposed, and both of them have a similar conversion mechanism.

Hydrothermal in situ synthesis of Rb and S co-doped Ti-based TiO2 sheet with a thin film showing high photocatalytic activities.

TiO2 is considered as one of the most promising semiconductor photocatalysts used to degrade organic pollutants. Element doping has a good effect on improving the properties of TiO2. Herein, by using Rb2SO4, we explored the in situ synthesis of Ti-based TiO2 sheets with a thin film through a hydrothermal reaction. Then, the photocatalyst was successfully fabricated by calcination. All samples were characterized by FT-IR, XRD, SEM, XPS, PL and UV-vis DRS measurements. The results indicate that the S doping together with surface hydroxyl groups lead to the band gap narrowing. S and a trace amount of Rb element can enable the formation of uniform microspheres on the surface of the Ti plate and the major phase transformed from titanium to anatase. The band gap absorption extended from 400 nm to 600 nm. The photocatalytic properties were investigated by performing the degradation of methyl orange (MO) and 4-chlorophenol (4-CP) in the aqueous solutions under UV and simulated sunlight. In the series of TiO2 photocatalysts, Rb/S/TiO2-48 shows the best photocatalytic efficiency and good photocatalytic performance on recycling. Interestingly, when H2O2 was added to the MO aqueous solution, a synergistic effect of the TiO2 thin film and H2O2 on degrading the pollutant was observed.