Liushui Yan

Preparation of graphene/TiO2 composites by nonionic surfactant strategy and their simulated sunlight and visible light photocatalytic activity towards representative aqueous POPs degradation

A series of graphene/TiO2 composites were fabricated using a single-step nonionic surfactant strategy combined with the solvothermal treatment technique. Their phase structure, morphology, porosity, optical absorption property, as well as composition and structure, were characterized. The as-prepared composites were successfully applied to degrade aqueous persistent organic pollutants (POPs) such as rhodamine B, aldicarb, and norfloxacin in simulated sunlight (λ>320 nm) and visible light (λ>400 nm) irradiation. The degradation mechanism and kinetics of aqueous POPs were studied in detail. The mineralization of aqueous POPs and the recyclability of the composites were also tested in the same condition.

Separation of flavanone enantiomers and flavanone glucoside diastereomers from Balanophora involucrata Hook. f. by capillary electrophoresis and reversed-phase high-performance liquid chromatography on a C18 column.

A pair of flavanone glucoside diastereomers, (2R)- and (2S)-eriodictyol-5-O-beta-d-glucopyranoside (1a, 1b), was successfully separated by RP-C(18) high-performance liquid chromatography from Balanophora involucrata Hook. f. Some other compounds, including a pair of flavanone enantiomers, (2R)- and (2S)-eriodictyol (2a, 2b), and a pair of flavanone glucoside diastereomers, (2R)- and (2S)-eriodictyol-7-O-beta-d-glucopyranoside(3a, 3b), were separated by capillary electrophoresis from the same plant. The absolute configurations at C-2 of 1a and 1b were determined based on their circular dichroism spectra. Enzymatic hydrolysis of 1a and 1b by beta-d-glucosidase afforded (2R)- and (2S)-eriodictyol, respectively, which were used as the authentic standards for co-elution to determine the migration order of the enantiomers, 2a and 2b. We also report the first example of identifying the migration order of 2a and 2b and resolving the separation of 3a and 3b by capillary electrophoresis. In addition, 1a was unambiguously characterized for the first time by NMR spectra.

Novel molecularly imprinted polymer using 1-(α-methyl acrylate)-3-methylimidazolium bromide as functional monomer for simultaneous extraction and determination of water-soluble acid dyes in wastewater and soft drink by solid phase extraction and high performance liquid chromatography

Novel water-compatible molecularly imprinted polymers were synthesized in methanol-water systems with Tratarzine as template and 1-(α-methyl acrylate)-3-methylimidazolium bromide (1-MA-3MI-Br) as functional monomer, which has π-π hydrophobic, hydrogen-bonding and electrostatic interactions with template molecule. 1-MA-3MI-Br molecularly imprinted polymers (1-MA-3MI-Br-MIPs) were used as selective sorbents for the solid-phase extraction (SPE) of water-soluble acid dyes from wastewater and soft drink. The good linearity of the method was obtained in a range of 5.0-2000 μg/L with the correlation coefficient of > 0.999. The detection limits were in a range of 0.13-0.51 μg/L for the water-soluble acid dyes in wastewater and 0.095-0.84 μg/L for those in soft drink. The mean recoveries for the acid dyes are from 89.1% to 101.0% in spiked wastewater and 91.0-101.3% in spiked soft drink. Compared with strongly anion exchange solid phase extraction (SAX-SPE), mixture anion exchange solid phase extraction (MAX-SPE), and 1-MA-3MI-Br non-imprinted solid phase extraction (1-MA-3MI-Br-NISPE), almost all of the matrix interferences were removed by 1-MA-3MI-Br-MISPE, exhibiting higher selectivity, recovery and enrichment ability for the acid dyes and better baselines in the results of HPLC analysis.

Determination of malachite green in fish water samples by cloud‐point extraction coupled to cation‐selective exhaustive injection and sweeping‐MEKC

We have employed a high‐sensitivity off‐line coupled with on‐line preconcentration method, cloud‐point extraction (CPE)/cation‐selective exhaustive injection (CSEI) and sweeping‐MEKC, for the analysis of malachite green. The variables that affect CPE were investigated. The optimal conditions were 250 g/L of Triton X‐100, 10% of Na2SO4 (w/v), heat‐assisted at 60°C for 20 min. We monitored the effects of several of the CSEI‐sweeping‐MEKC parameters – including the type of BGE, the concentrations of SDS, the injection length of the high‐conductivity buffer, and the injection time of the sample – to optimize the separation process. The optimal BGE was 50 mM citric acid (pH 2.2) containing 100 mM SDS. In addition, electrokinetic injection of the sample at 15 kV for 800 s provided both high separation efficiency and enhanced sweeping sensitivity. The sensitivity enhancement for malachite green was 1.9×104 relative to CZE; the coefficients of determination exceeded 0.9928. The LOD, based on an S/N of 3:1, of CSEI‐sweeping‐MEKC was 0.87 ng/mL; in contrast, when using off‐line CPE/CSEI‐sweeping‐MEKC the sensitivity increased to 69.6 pg/mL. This proposed method was successfully applied to determine trace amounts of malachite green in fish water samples.

Fabrication of carbon nitride nanotubes by a simple water-induced morphological transformation process and their efficient visible-light photocatalytic activity

Carbon nitride nanotubes (C3N4 NTs) were synthesized based on the nanosheets roll-up mechanism by a simple water-induced morphological transformation process using graphitic carbon nitride (g-C3N4) as a precursor. Water was used as the phase-transfer reagent, making the preparation process environmentally friendly. The visible-light photocatalytic activity of the as-prepared C3N4 NTs significantly increased compared to bulk g-C3N4 and g-C3N4 nanosheets toward rhodamine B degradation and hydrogen evolution from water-splitting. This result can be attributed to the high photogenerated carrier transfer efficiency, excellent mass transfer capability, sufficient active sites, and enhanced light utilization efficiency of C3N4 NTs.

Fabrication of porous g-C 3 N 4 and supported porous g-C 3 N 4 by a simple precursor pretreatment strategy and their efficient visible-light photocatalytic activity

Porous g-C 3 N 4 and supported porous g-C 3 N 4 were fabricated for the first time by a simple strategy using pretreated melamine as a raw material and pretreated quartz rod as a substrate. The formation of a richly porous microstructure can be attributed to the co-existence of different pore-fabricating units in the preparation system for porous g-C 3 N 4 . The richly porous microstructure endowed the as-prepared porous g-C 3 N 4 with an excellent photocatalytic activity. The as-prepared supported porous g-C 3 N 4 exhibited considerable stability because of the existence of chemical interaction between porous g-C 3 N 4 and the quartz rod substrate. The photocatalytic activity of the supported porous g-C 3 N 4 was competitive with that of porous g-C 3 N 4 in powder form because neither the surface migration of photogenerated electrons nor the diffusion of the target organic pollutant were affected by the construction of the quartz rod reactor. The photocatalytic activity of the as-prepared porous g-C 3 N 4 and supported porous g-C 3 N 4 was preliminarily evaluated by the treatment of single-component organic wastewater under visible-light irradiation. Subsequently, the as-prepared porous g-C 3 N 4 was further applied in conventional hydrogen evolution and a new system for simultaneous hydrogen evolution with organic-pollutant degradation. The hydrogen yield and degradation efficiency both increased with increasing photocatalytic activity of the as-prepared materials in the system for simultaneous hydrogen evolution with organic-pollutant degradation.

Fabrication of highly dispersed platinum-deposited porous g-C3N4 by a simple in situ photoreduction strategy and their excellent visible light photocatalytic activity toward aqueous 4-fluorophenol degradation

A series of highly dispersed platinum-deposited porous g-C 3 N 4 (Pt/pg-C 3 N 4 ) were successfully fab-ricated by a simple in situ photoreduction strategy using chloroplatinic acid and porous g-C 3 N 4 as precursors. Porous g-C 3 N 4 was fabricated by a pretreatment strategy using melamine as a raw ma-terial. The morphology, porosity, phase, chemical structure, and optical and electronic properties of as-prepared Pt/pg-C 3 N 4 were characterized. The photocatalytic activity of as-prepared Pt/pg-C 3 N 4 was preliminarily evaluated by the degradation of aqueous azo dyes methyl orange under visible light irradiation. The as-prepared Pt/pg-C 3 N 4 were further applied to the degradation and mineral-ization of aqueous 4-fluorophenol. The recyclability of Pt/pg-C 3 N 4 was evaluated under four con-secutive photocatalytic runs.

Surface molecular imprinting on carbon microspheres for fast and selective adsorption of perfluorooctane sulfonate

Perfluorooctane sulfonate (PFOS) is a persistent organic pollutant with high biological and chemical stability. It is important to develop fast and selective adsorption method for PFOS wastewater treatment. In this study, novel molecularly imprinted polymer (MIP) for PFOS adsorption was prepared. To obtain rapid adsorption kinetics, the MIP has been designed as the surface polymer using the carbon microsphere as carrier (MIP-CMSs). To ensure high adsorption selectivity to the template, two monomers with different functional structures, namely methacryloyloxyethyl trimethyl ammonium chloride (DMC) and 2-(trifluoromethyl)acrylic acid (TFMA), were employed as bi-functional monomers. The structure and morphology of MIP-CMSs were characterized using field emission scanning electron microscopy with the energy dispersive spectrometer, transmission electron microscopy, and Fourier transformation infrared spectroscopy. Based on the adsorption experiments, it was concluded that MIP-CMSs had specific binding property for PFOS on acidic condition. The adsorption equilibrium time was 1h, while the adsorption capacity was 75.99 mg g-1 at pH 3. Coexistence with contaminants with different structures had little influence on the selectivity for PFOS. The spent MIP-CMSs could be regenerated by the methanol and acetic acid mixed solution. The electrostatic interaction and molecular size played important roles in recognizing the target compound in the adsorption process.