Shisuo Fan

Phosphorus removal and N2O production in anaerobic/anoxic denitrifying phosphorus removal process: Long-term impact of influent phosphorus concentration

This study was conducted to investigate the long-term impact of influent phosphorus concentration on denitrifying phosphorus removal and N2O production during denitrifying phosphorous removal process. The results showed that, denitrifying phosphate accumulating organisms (DPAOs) could become dominant populations quickly in anaerobic/anoxic SBR by providing optimum cultivating conditions, and the reactor performed well for denitrifying phosphorus removal. The influent phosphorus concentration significantly affected anaerobic poly-β-hydroxyalkanoates (PHA) synthesis, denitrifying phosphorus removal, and N2O production during the denitrifying phosphorus removal process. As the influent phosphorus concentration was more than 20 mg L(-1), the activity of DPAOs began to be inhibited due to the transformation of the available carbon source type. Meanwhile, N2O production was inhibited with the mitigation of anoxic NO2(-)-N accumulation. Adoption of a modified feeding could enhance denitrifying phosphorus removal and inhibit N2O production during denitrifying phosphorous removal processes.

Facile synthesis of tea waste/Fe3O4 nanoparticle composite for hexavalent chromium removal from aqueous solution

The modification of biomass waste, as a multifunctional composite, has received tremendous attention for resource utilization and recycling. In this study, tea waste, which is a high level generator of biomass waste, was loaded with nano-Fe3O4 particles to prepare a magnetic tea waste/Fe3O4 (TW/Fe3O4) composite through a facile chemical co-precipitation approach. BET, SEM, TEM, XRD, magnetic properties, FTIR, XPS were used to characterize the TW/Fe3O4 composite. A superparamagnetic TW/Fe3O4 composite (Fe3O4: about 20 nm) was successfully synthesized and possessed the advantages of tea waste and nano-Fe3O4 particles. A chromium(VI) adsorption experiment showed that this material has a strong adsorption capacity for aqueous chromium ions, which reached 75.76 mg g−1 based on the Langmuir model. The adsorption process could be well fitted by a pseudo-second-order kinetic model and Langmuir, Temkin and Dubinin–Radushkevich (D–R) isotherm models, and was spontaneous and endothermic according to the thermodynamic analysis. The TW/Fe3O4 composite revealed good reusability and the removal rate was more than 70% after five recycling cycles. The mechanism of Cr(VI) removal involved electrostatic attraction, reduction process, ion exchange, surface complexation, etc. 70% of Cr(VI) was reduced to Cr(III) in this investigation. This study indicated that a TW/Fe3O4 composite could be an attractive option for heavy metal treatment.

A Simple and Effective Ratiometric Fluorescent Probe for the Selective Detection of Cysteine and Homocysteine in Aqueous Media.

Biothiols such as cysteine (Cys) and homocysteine (Hcy) are essential biomolecules participating in molecular and physiological processes in an organism. However, their selective detection remains challenging. In this study, ethyl 2-(3-formyl-4-hydroxyphenyl)-4-methylthiazole-5-carboxylate (NL) was synthesized as a ratiometric fluorescent probe for the rapid and selective detection of Cys and Hcy over glutathione (GSH) and other amino acids. The fluorescence intensity of the probe in the presence of Cys/Hcy increased about 3-fold at a concentration of 20 equiv. of the probe, compared with that in the absence of these chemicals in aqueous media. The limits of detection of the fluorescent assay were 0.911 μM and 0.828 μM of Cys and Hcy, respectively. 1H-NMR and MS analyses indicated that an excited-state intramolecular proton transfer is the mechanism of fluorescence sensing. This ratiometric probe is structurally simple and highly selective. The results suggest that it has useful applications in analytical chemistry and diagnostics.

Comparative Studies of Interactions between Fluorodihydroquinazolin Derivatives and Human Serum Albumin with Fluorescence Spectroscopy

In the present study, 3-(fluorobenzylideneamino)-6-chloro-1-(3,3-dimethylbutanoyl)-phenyl-2,3-dihydroquinazolin-4(1H)-one (FDQL) derivatives have been designed and synthesized to study the interaction between fluorine substituted dihydroquinazoline derivatives with human serum albumin (HSA) using fluorescence, circular dichroism and Fourier transform infrared spectroscopy. The results indicated that the FDQL could bind to HSA, induce conformation and the secondary structure changes of HSA, and quench the intrinsic fluorescence of HSA through a static quenching mechanism. The thermodynamic parameters, ΔH, ΔS, and ΔG, calculated at different temperatures, revealed that the binding was through spontaneous and hydrophobic forces and thus played major roles in the association. Based on the number of binding sites, it was considered that one molecule of FDQL could bind to a single site of HSA. Site marker competition experiments indicated that the reactive site of HSA to FDQL mainly located in site II (subdomain IIIA). The substitution by fluorine in the benzene ring could increase the interactions between FDQL and HSA to some extent in the proper temperature range through hydrophobic effect, and the substitution at meta-position enhanced the affinity greater than that at para- and ortho-positions.

Biointeractions of Herbicide Atrazine with Human Serum Albumin: UV-Vis, Fluorescence and Circular Dichroism Approaches

The herbicide atrazine is widely used across the globe, which is a great concern. To investigate its potential toxicity in the human body, human serum albumin (HSA) was selected as a model protein. The interaction between atrazine and HSA was investigated using steady-state fluorescence spectroscopy, synchronous fluorescence spectroscopy, UV-Vis spectroscopy, three-dimensional (3D) fluorescence spectroscopy and circular dichroism (CD) spectroscopy. The intrinsic fluorescence of HSA was quenched by the atrazine through a static quenching mechanism. Fluorescence spectra at two excitation wavelengths (280 and 295 nm) showed that the fluorescence quenched in HSA was mainly contributed to by tryptophan residues. In addition, the atrazine bound to HSA, which induced changes in the conformation and secondary structure of HSA and caused an energy transfer. Thermodynamic parameters revealed that this binding is spontaneous. Moreover, electrostatic interactions play a major role in the combination of atrazine and HSA. One atrazine molecule can only bind to one HSA molecule to form a complex, and the atrazine molecule is bound at site II (subdomain IIIA) of HSA. This study furthers the understanding of the potential effects posed by atrazine on humans at the molecular level.

Removal Behavior of Methylene Blue from Aqueous Solution by Tea Waste: Kinetics, Isotherms and Mechanism

Tea waste (biosorbent) was characterized by BET, SEM, FTIR, XPS, solid state 13C-NMR and applied to remove methylene blue (MB) from aqueous solution. The effect of different factors on MB removal, kinetics, isotherms and potential mechanism was investigated. The results showed that tea waste contains multiple organic functional groups. The optimum solid-to-liquid ratio for MB adsorption was 4.0 g·L−1 and the initial pH of the MB solution did not need to be adjusted to a certain value. The pseudo-second-order model could well fit the adsorption kinetic process. The adsorption process could be divided into two stages: a fast adsorption stage and a slow adsorption stage. The adsorption isotherm could be well described by Langmuir and Temkin isotherm models. The maximum adsorption amount could reach 113.1461 mg·g−1 based on Langmuir isotherm fitting. Desorption and reusability experiments showed that MB adsorption onto tea waste could be stable and could not cause secondary pollution. The interaction mechanism between tea waste and MB involved electrostatic attraction, hydrogen bond, ion exchange, π-π binding. The organic functional groups of tea waste played an important role during the MB removal process. Therefore, tea waste has the potential to act as an adsorbent to remove MB from aqueous solution.

Oxalate Enhances Desorption of Perfluorooctane Sulfonate from Soils and Sediments

Perfluorooctane sulfonate (PFOS) is one of the most widespread toxic substances in water distribution systems, posing a significant risk to public health and the environment due to its toxic and non-biodegradable nature. In this study, the effect of oxalate on PFOS adsorption/desorption to/from soil and sediment samples was studied with batch experiments. Dissolved organic carbon content in soil strongly enhanced the retention of organic halogens. Oxalate increased PFOS desorption by 1.43- to 17.14-fold and significantly increased the release of dissolved organic carbon and inorganic ions in soils. The effects of root exudates were similar to those of oxalate. Addition of low molecular weight dissolved organic carbon caused partial dissolution of the soil structure (e.g., through formation of organo-mineral complexes), resulting in the release of organic carbon and metal ions and subsequently enhancing PFOS desorption. The effects of oxalate on organic halogen desorption were influenced by dissolved organic carbon content and formation of calcium oxalate.