A High-Affinity and Removable Iminium Dication Guest for Recycling of Cucurbit[7]uril Materials.

An iminium dication 1 was designed as a high-affinity and easily removable guest for cucurbit[7]uril (CB[7]). X-ray crystallographic analysis shows that maximized N+···O═C ion-dipole interactions and perfect packing coefficient are responsible for the high affinity of 1 for CB[7] (Ka > 1011 M-1). Under alkaline conditions, included 1 in CB[7]·1 is hydrolyzed into 2,6-adamantanedione and pyrrolidine that can be fully removed by further extraction, enabling the recycling of CB[7] materials.

Degradation of acid red 73 wastewater by hydrodynamic cavitation combined with ozone and its mechanism.

Many azo dyes are consumed in the textile and dyeing industry, which makes the wastewater recalcitrant and toxic to the aquatic environment. Dye degradation by the combination of hydrodynamic cavitation and ozone (HC + O3) has caused extensive interest. The degradation mechanism of the hybrid system needs further investigation. This study investigated the degradation of acid red 73 (AR73) by HC + O3. Meanwhile, the degradation pathways and mechanisms were present. The optimal operation parameters were: inlet pressure of 0.15 MPa, O3 dosage of 45 mg/min, initial dye concentration of 10 mg/L, and initial pH at 7.5. As a result, the decolorization rate, removal of UV254 and NH3-N were 100%, 71.28%, and 87.36% in 30 min, respectively. Humic acid and most of the co-existing anions (HCO3-, SO42-, Cl-, PO43-, NO3-) played a positive role in the degradation of AR73, while NO2- restrained. The reactive species of singlet oxygen (1O2), hydroxyl radicals (·OH) and super oxygen radicals (·O2-) showed synergism in the hybrid system, and the decolorization was attributed to the fracture of azo bonds by 1O2. Meanwhile, aromatic amines were generated and further degraded into small molecule compounds. The research certificated that the HC + O3 can be an effective technology for azo dye degradation.

[Using size-exclusion chromatography to quantify the 146S antigen in inactivated foot-and-mouth disease vaccine].

The aim of this study is to quantify the 146S antigen in foot-and-mouth disease virus (FMDV) inactivated vaccine by size-exclusion chromatography (SEC). The analysis was performed on a TSKgel G4000SWXL column (7.8 mm×30 cm), with a pH 7.2 buffer salt system as the mobile phase. The flow rate was 0.6 mL/min, the injection volume was 100 µL and the detection wavelength was 259 nm. The calibration curve was established by using purified inactivated FMDV (serotype O) 146S antigen; 3 batches of vaccine formulated by inactivated antigen solution were tested to verify the accuracy, reproducibility, specificity and tolerability of the method. At last 16 batches of vaccine were determined by the SEC method. Results showed a good linearity between peak area and concentration of 146S antigen in the range between 0.56 and 67.42 µg/mL (R2=0.996, n=10), and the average recovery rate of 146S antigen in the 3 batches of vaccine formulated in lab were 93.6% (RSD=2.7%, n=3), 102.3% (RSD=2.6%, n=3), and 95.5% (RSD=5.1%, n=3). The method was proved accurate and reliable with good reproducibility (RSD=0.5%, n=6), and applied to determine 16 batches of the commercial FMDV vaccine. According to the above results, the SEC method is high effective for 146S antigen quantify in the inactivated FMDV vaccine and would provide strong support for the vaccine quality control.