A preliminary attempt at capacitive deionization with PVA/PSS gel coating as an alternative to ion exchange membrane.

PVA/PSS composite gel membrane electrode for membrane capacitive deionization (MCDI) was fabricated and characterised in the present study. The composite electrode with ion exchange surface is prepared by coating glutaraldehyde cross-linked polyvinyl alcohol (PVA) composite hydrogel, with Poly (Sodium 4-Styrenesulfonate) (PSS) added into the network, on the surface of activated carbon (AC) electrode. The feasibility of the gel membrane is analyzed by rheological, swelling rates and ion exchange capacity tests. Then electrochemical test and desalination test are used to study the performance of the MCDI electrode. The results show that coating of composite hydrogel layer improved the hydrophilicity, specific capacitance and lower interfacial electron transfer resistance of the electrode. Finally, we assemble the asymmetrical CDI cell with PVA/PSS composite gel electrode and AC electrode. Compared with the AC electrode, the salt adsorption capacity of PVA6-PSS15 can reach 18.9 mg g-1 and stable charge efficiency at 73.0% at operating voltage of 1.2 V. The decrease in specific capacitance of PVA6-PSS15 after 50 cycles is 1.33%, indicating that the electrode has a good cycling life. The gel membrane coated electrode prepared by PSS provides a new idea for the development of MCDI.

Low-nitrite generation Cu-Co/Ti cathode materials for electrochemical nitrate reduction.

In order to reduce by-product nitrite, a more toxic compound than nitrate, and increase high value-added products ammonia in the electrochemical reduction nitrate process, the novel Cu-Co/Ti cathode material was applied in this process. In this paper, the electrochemical process was carried out in a single compartment electrolytic cell, and with Cu-Co/Ti electrode as cathode, identifying the effects of current density, pH, electrolytes in the nitrate reduction, and the distribution of products. The Cu-Co/Ti cathode exhibited 94.65% NO3--N (nitrate-N) removal, 0.18% NO2--N (nitrite-N) generation, and 40.86% NH4--N (ammonia-N) generation with the assistance of Na2SO4 electrolyte in 6 h at 10 mA cm-2 and pH 6. Compared with the Cu/Ti cathode, the higher nitrate removal ratio and lower nitrite generation ratio were obtained on the Cu-Co/Ti cathode. The excellent performance of Cu-Co/Ti cathode is ascribed to the synergy of Cu and Co, which couples the facilitation of nitrate conversion to nitrite and the acceleration of nitrite reduction on the Cu-Co/Ti cathode. The LSV curves showed that nitrate and nitrite might undergo indirect and direct reduction reactions on Cu-Co/Ti cathode. The possible pathways of nitrate reduction on the Cu-Co/Ti cathodes were proposed. These results highlight the viability of using the Cu-Co/Ti cathode developed at this work for the nitrate removal from contaminated waters. This study achieved low-nitrite generation by Cu-Co/Ti cathode during electrochemical nitrate reduction.

Effect of anion-exchange membrane type for FCDI performance at different concentrations.

Brackish water was an important alternative source of freshwater. Desalination using flow electrode capacitive deionization (FCDI) needs to explore the role of ion exchange membranes (IEM) of FCDI. In this study, brackish water was desalinated using FCDI, and anion exchange membranes with different characteristics were used in the FCDI cell to investigate their influence. The result showed that the membrane polymer matrix was the main influencing factor for ion transport. Ion exchange capacity (IEC) has a huge impact that low IEC made the various ion transport priority. Low IEC not only limits ion transport but also leads to ion leakage in seawater. Resistance had a significant blockage to the effect with weak intensity.

Electrochemical degradation of chloramphenicol using Ti-based SnO2-Sb-Ni electrode.

Antibiotic residues may be very harmful in aquatic environments, because of limited treatment efficiency of traditional treatment methods. An electrochemical system with a Ti-based SnO2-Sb-Ni anode was developed to degrade a typical antibiotic chloramphenicol (CAP) in water. The electrode was prepared using a sol-gel method. The performance of electrode materials, impact factors and dynamic characteristics were evaluated. The Ti-based SnO2-Sb-Ni electrode was compact and uniform as shown by characterization using SEM and XRD. The electrocatalytic oxidation of CAP was carried out in a single-chamber reactor by using a Ti-based SnO2-Sb-Ni electrode. For 100 mg L-1 CAP, the CAP removal ratio of 100% and the TOC removal ratio of 60% were obtained at the current density of 20 mA cm-2 and in a neutral electrolyte at 300 min. Kinetic investigation has shown that the electro-oxidation of CAP on a Ti-based SnO2-Sb-Ni electrode displayed a pseudo-first-order kinetic model. Free radical quenching experiments presented that the oxidation of CAP on Ti-based SnO2-Sb-Ni electrode resulted from the synergistic effect of direct oxidation and indirect oxidation (·OH and ·SO4-). Doping Ni on the Ti/SnO2-Sb electrode for CAP degradation was presented in this paper, showing its great application potential in the area of antibiotic and halogenated organic pollutant degradation.

Preparation of a novel Cu-Sn-Bi cathode and performance on nitrate electroreduction.

Cu-Sn-Bi layer coated on Ti substrate was prepared using electrodeposition method and applied as cathode material for electrochemical reduction of nitrate in this research. Linear sweep voltammetry (LSV), chronoamperometry (CA), scanning electron microscope (SEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD) were used to scrutinize the electrochemical performance and the cathode materials. LSV results illustrated that Cu-Sn-Bi cathode possessed the ability for nitrate reduction. Preparation conditions including deposition time, current density, temperature and the content of Bi were optimized based on NO3 -N removal and byproducts selectivity. Results showed that the cathode with Bi content of 3.18 at.%, and electrodepositing at current density of 6 mA cm-2, 35 °C for 30 min achieved the best performance during the experiment. The increase of Bi content could improve the electrocatalytic activity and stability of the cathode. Compared with other common researched cathodes (Cu and Fe), Cu-Sn-Bi (3.18 at.%) exhibited better performance, i.e. the highest NO3 -N removal of 88.43% and the selectivity of harmless N2 was 77.80%. The kinetic studies showed that the reduction of nitrate on Cu-Sn-Bi followed pseudo-first-order kinetics.

Removal of Pb(II) from aqueous solutions by adsorption on magnetic bentonite.

Bentonite is a porous clay material that shows good performance for adsorbing heavy metals and other pollutants for wastewater remediation. In our previous study, magnetic bentonite (M-B) was prepared to solve the separation problem and improve the operability. In this study, we investigated the influence of various parameters on the Pb(II) adsorption of M-B, and it showed effective performance. About 98.9% adsorption removal rate was achieved within 90 min at adsorbent dose of 10 g/L for initial Pb(II) concentration of 200 mg/L at 40 °C and pH 5. The adsorption kinetic fit well by the pseudo-second-order model, and also followed the intra-particle diffusion model up to 90 min. Moreover, adsorption data were successfully reproduced by the Langmuir isotherm; the maximum adsorption capacity was calculated as 80.40 mg/g. The mechanism of interaction between Pb(II) ions and M-B was ionic exchange, surface complexation, and electro-static interactions. Thermodynamics study indicated that the reaction of Pb(II) adsorption on M-B was endothermic and spontaneous; increasing the temperature promoted adsorption. This study was expected to provide a reference and theoretical basis for the treatment of Pb-containing wastewater using bentonite materials.

Adsorption behavior of magnetic bentonite for removing Hg(ii) from aqueous solutions.

Bentonite is a porous clay material that shows good performance for adsorbing heavy metals and other pollutants for wastewater remediation. However, it is very difficult to separate the bentonite from water after adsorption as it forms a stable suspension. In this paper, we prepared magnetic bentonite (M-B) by loading Fe3O4 particles onto aluminum-pillared bentonite (Al-B) in order to facilitate its removal from water. The functional groups, skeleton structure, surface morphology and electrical changes of the prepared material were investigated by FT-IR, XRD, BET, SEM, VSM and zeta potential measurements. It was used as an adsorbent for Hg(ii) removal from aqueous solutions and the influence of various parameters on the adsorption performance was investigated. The adsorption kinetics were best fitted by the pseudo-second-order model, and also followed the intra-particle diffusion model up to 18 min. Moreover, adsorption data were successfully reproduced by the Langmuir isotherm, and the Hg(ii) adsorption saturation capacity was determined as 26.18 mg g-1. The average adsorption free energy change calculated by the D-R adsorption isotherm model was 11.89 kJ mol-1, which indicated the occurrence of ionic exchange. The adsorption thermodynamic parameter ΔH was calculated as 42.92 kJ mol-1, which indicated chemical adsorption. Overall, the thermodynamic parameters implied that Hg(ii) adsorption was endothermic and spontaneous.

Hollow microsphere with mesoporous shell by Pickering emulsion polymerization as a potential colloidal collector for organic contaminants in water.

Submicrometer hollow microspheres with mesoporous shells were prepared by a simple one-pot strategy. Colloidal silica particles were used as a particle stabilizer to emulsify the oil phase, which was composed of a polymerizable silicon monomer (TPM) and an inert organic solvent (PEA). The low interfacial tension between colloidal silica particles and TPM helped to form a Pickering emulsion with small droplet sizes. After the polymerization of TPM, the more hydrophobic PEA formed a liquid core, leading to a hollow structure after its removal by evaporation. BET results indicated that the shell of a hollow particle was mesoporous with a specific surface area over 400 m(2)·g(-1). With PEA as the core and silica as the shell, each resultant hollow particle had a hydrophobic cavity and an amphiphilic surface, thus serving as a good colloidal collector for hydrophobic contaminants in water.

Facile preparation route toward speckled colloids via seeded polymerization.

A facile method to prepare monodisperse speckled colloids has been developed via one-step seeded polymerization from noncross-linked latex particles. It was found that both cross-linking agents in the added monomer mixture and charged initiation species are essential for the formation of speckles on composite latex particle surface in seeded polymerization. The size and number density of speckles on the surface are tunable by adjusting the concentration of surfactant. A possible mechanism for the formation of such speckled colloids has been proposed based on a series of control experiments. Speckled colloidal particles were used as substrates for the adsorption of tobacco mosaic virus, and a much stronger adsorption was observed compared to smooth particles, implying a potential application of these speckled particles in virus collection and more.

Fabrication of a composite colloidal particle with unusual Janus structure as a high-performance solid emulsifier.

Core-shell particles with cross-linked core and shell were used as seed particles to produce composite Janus particles. It was found that when the shell has distinctly higher cross-linking degree than the core, Janus particles with very unusual structures can be obtained. These particles have two parts, with one part embraced partially or entirely by the other part, adjustable by parameters such as phase ratio or cross-linking degree. On the basis of experimental observations, a possible mechanism for the formation of such unusual Janus particles has been proposed. Janus particles with arms are used to emulsify water-toluene mixtures, forming oil-in-water (O/W) emulsions at very high internal phase content with rather low concentration of particles. Nonspherical emulsion droplets were observed, indicating that these Janus particles are likely to jam at the interface, forming a strong protecting layer to stabilize emulsions.