Preparation of Sepiolite Nanofibers Supported Zero Valent Iron Composite Material for Catalytic Removal of Tetracycline in Aqueous Solution

The heavy use of antibiotics in medicine, stock farming and agriculture production has led to their gradual accumulation in environmental media, which poses a serious threat to ecological environment and human safety. As an efficient and promising catalyst for the degradation of antibiotics, nanoscale zero valent iron (nZVI) has attracted increasing attention in recent years. In this study, sepiolite nanofiber supported zero valent iron (nZVI/SEP) composite was prepared via a facile and environmentally friendly method. The nZVI particles (with size of 20–60 nm) were dispersed evenly on the surface of sepiolite nanofibers, and the catalytic performance for the removal of tetracycline hydrochloride (TC-HCl) in aqueous system was investigated. The effect of nZVI loading amount, catalyst dosage, H2O2 concentration and pH on the removal efficiency of TC-HCl were studied. It was revealed that the sepiolite supporter effectively inhibited the agglomeration of nZVI particles and increased the contact area between contaminant and the active sites, resulting in the higher catalytic performance than pure nZVI material. The TC-HCl removal efficiency of nZVI/SEP composite was up to 92.67% when TC-HCl concentration of 20 mg/L, catalyst dosage of 1.0 g/L, H2O2 concentration of 1.0 mM, pH value of 7. Therefore, the nZVI/SEP composites possess high catalytic activity for TC-HCl removal and have great application prospects in antibiotic wastewater treatment.

A novel route for aspartame production by combining enzymatic and chemical reactions for industrial use

ABSTRACT Here, we report a novel industrial aspartame production route, involving the enzymatic production of α-l-aspartyl-l-phenylalanine β-methylester from l-aspartic acid dimethylester and l-phenylalanine by α-amino acid ester acyl transferase. The route also involves the chemical transformation of α-l-aspartyl-l-phenylalanine β-methylester to α-l-aspartyl-l-phenylalanine methylester hydrochloride (aspartame hydrochloride) in an aqueous solution with methanol and HCl, followed by HCl removal to form aspartame.

HCl Removal Using Calcined Ca–Mg–Al Layered Double Hydroxide in the Presence of CO2 at Medium–High Temperature

This present work aimed to investigate the influence of CO2 on HCl removal using calcined Ca–Mg–Al layered double hydroxides (CaMgAl-LDHs) at medium–high temperature (400–800 °C) in a fixed-bed reactor. It was revealed that a moderate CO2 concentration (~6%) in the flue gas of the municipal solid-waste incinerators could reduce the HCl capacity of the CaMgAl-layered double oxides (CaMgAl-LDOs). The highest capacity for HCl removal was observed over the CaMgAl-LDOs at 600 °C. However, sintering was also detected when the reaction temperature was below the calcination temperature (600 °C). Moreover, the decreasing HCl adsorption capacity of CaMgAl-LDOs was attributed to the existence of CO2 in the flue gas, which could efficiently inhibit the decomposition of carbonates as well as the conversion into metal chloride during the HCl removal process.