Jiangsu Higher Education Institutions

Suzhou, China

Jiangsu Higher Education Institutions

Suzhou, China
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Xu M.,Soochow University of China | Han X.,Soochow University of China | Hua D.,Soochow University of China | Hua D.,Jiangsu Higher Education Institutions
Journal of Materials Chemistry A | Year: 2017

The competition between uranium ions and other metal ions is one of the great challenges for recovery of uranium(vi) from seawater. In particular, vanadium ions that bind strongly to sorbents are hardly stripped off, largely decreasing the sorption capability of the sorbents for uranium. In this study, polyoxime was, for the first time, designed and conjugated onto magnetic nanoparticles for selective sorption of uranium(vi) against vanadium. Magnetic iron oxide nanoparticles were first grafted with polyglycerol on the surface, and then conjugated with oxime groups via esterification and oximation to give polyoxime-functionalized magnetic nanoparticles (POMNs). POMNs showed superior aqueous dispersibility and could be readily recovered by magnetic separation. The uranium(vi) sorption of POMNs achieved equilibrium in 5 min with a capacity of 141.4 mg g-1 in a single-element solution of uranium at pH 8.0 and 298.15 K. The sorption in simulated seawater demonstrated that the POMNs possessed excellent selectivity for uranium(vi) against vanadium(v) and other competing metal ions. No significant change in sorption efficiency and selectivity for uranium was observed following four sorption-desorption cycles using Na2CO3 solution as an eluent. This work may unfold a new approach for selective sorption of uranium in seawater. © 2017 The Royal Society of Chemistry.

Shao D.,North China Electrical Power University | Shao D.,Soochow University of China | Li J.,North China Electrical Power University | Wang X.,North China Electrical Power University | And 2 more authors.
Science China Chemistry | Year: 2014

The development of efficient materials for high extraction of uranium (UO2 2+) from seawater is critical for nuclear energy. Poly(amidoxime)-reduced graphene oxide (PAO/rGO) composites with excellent adsorption capability for UO2 2+ were synthesized by in situ polymerization of acrylonitrile monomers on GO surfaces, followed by amidoximation treatment with hydroxylamine. The adsorption capacities of PAO/rGO composites for UO2 2+ reached as high as 872 mg/g at pH 4.0. The excellent tolerance of these composites for high salinity and their regeneration-reuse properties can be applied in the nuclear-fuel industry by high extraction of trace UO2 2+ ions from seawater. © 2014 Science China Press and Springer-Verlag Berlin Heidelberg.

Wei Y.,Soochow University of China | Wang Y.,Soochow University of China | Zeng Z.,Soochow University of China | Zhang S.,Soochow University of China | And 2 more authors.
Polymer (United Kingdom) | Year: 2014

The colloidal particles with switchable surfaces (i.e. smart surfaces) have attracted great attention for numerous potential industrial applications. We report here a novel approach for the fabrication of polymeric particles with smart surfaces by emulsion polymerization using "giant" surfactant. Specifically, the "giant" surfactant was obtained by incorporating poly(4-vinylpyridine) chains onto the one bulb of snowman-shaped polystyrene particles, and then used as emulsifier for the emulsion polymerization at pH = 2.00. The nearly monodisperse waxberry-like polystyrene particles were prepared with dual-size roughness surfaces, and the particulate film exhibited reversibly pH-switchable superhydrophobic property due to the pH-sensitivity of P4VP chains and the surface topology. This property enabled the particles could be used to effectively sequester hazardous anions from the wastewater. © 2014 Elsevier Ltd. All rights reserved.

Zhang S.,North China Electrical Power University | Zhang S.,Hefei University of Technology | Li J.,North China Electrical Power University | Li J.,Jiangsu Higher Education Institutions | And 7 more authors.
ACS Applied Materials and Interfaces | Year: 2014

A novel efficient Ag@AgCl/g-C3N4 plasmonic photocatalyst was synthesized by a rational in situ ion exchange approach between exfoliated g-C3N4 nanosheets with porous 2D morphology and AgNO3. The as-prepared Ag@AgCl-9/g-C3N4 plasmonic photocatalyst exhibited excellent photocatalytic performance under visible light irradiation for rhodamine B degradation with a rate constant of 0.1954 min-1, which is ∼41.6 and ∼16.8 times higher than those of the g-C3N4 (∼0.0047 min-1) and Ag/AgCl (∼0.0116 min-1), respectively. The degradation of methylene blue, methyl orange, and colorless phenol further confirmed the broad spectrum photocatalytic degradation abilities of Ag@AgCl-9/g-C3N4. These results suggested that an integration of the synergetic effect of suitable size plasmonic Ag@AgCl and strong coupling effect between the Ag@AgCl nanoparticles and the exfoliated porous g-C3N4 nanosheets was superior for visible-light-responsive and fast separation of photogenerated electron-hole pairs, thus significantly improving the photocatalytic efficiency. This work may provide a novel concept for the rational design of stable and high performance g-C3N4-based plasmonic photocatalysts for unique photochemical reaction. © 2014 American Chemical Society.

Shu X.,Soochow University of China | Wang Y.,Soochow University of China | Zhang S.,Soochow University of China | Huang L.,Soochow University of China | And 3 more authors.
Talanta | Year: 2015

Uranyl ion exists at trace levels in the environment and can cause severe adverse effects to human health. Therefore, it is desirable to develop analytical methods that can determine the trace uranyl ion in aqueous medium. We report here a new method using a thermo-responsive polymeric fluorescent sensor. Specifically, 5,10,15,20-tetrakis(4-carboxyphenyl)-porphyrin terminated poly(N-isopropylacrylamide) (TCPP-PNIPAM) was synthesized by controlled free radical polymerization for the detection of uranyl ion. The maximum fluorescence intensity at ~658 nm of TCPP-PNIPAM increases with molecular weights and is also closely related to the temperature. The polymeric sensor is sensitive to pH (1.0~5.0) with a fast responsive time (~3 min). Under optimized experimental conditions, the sensor exhibits a stable response for uranyl ion with high selectivity over a concentration range from 1.0×10-3 to 1.0×10-7 mol/L. For the trace uranyl ion (such as 1.0×10-8 or 10-9 mol/L), the determination could be successfully achieved after concentrating 100 times by centrifugation above 32 °C. The properties enable the polymeric sensor to have great potential for environmental application. © 2014 Elsevier B.V. All rights reserved.

Shu X.,Soochow University of China | Shu X.,Jiangsu Higher Education Institutions | Shen L.,Soochow University of China | Wei Y.,Soochow University of China | And 2 more authors.
Journal of Molecular Liquids | Year: 2015

It is significant for environment and human health to develop new materials for the sorption of radioactive technetium. We report herein a novel method to synthesize surface ion-imprinted magnetic microspheres for efficient capture of technetium ions. Specifically, perrhenate anion as the structural surrogate for pertechnetate anion, was employed as template to prepare ion-imprinted magnetic microsphere by "one-pot" radical polymerization and quaternization. The sorption behavior is closely related with the surface chemical composition: the more nitrogen content, the higher sorption efficiency. The sorption is an exothermic spontaneous sorption process and kinetically followed pseudo-second-order model. A sorption capacity of 62.8 mg of Re/g could be achieved at 298.15 K and pH = 6. Compared with non-imprinted composites, imprinted microspheres showed higher selectivity, faster kinetics, and larger sorption capacity of perrhenate ions. This work may provide a promising approach for the efficient sorption of pertechnetate. © 2015 Elsevier B.V. All rights reserved.

Zhou Y.,Soochow University of China | Hua S.,Jiangsu Higher Education Institutions | Yu J.,Jiangsu Higher Education Institutions | Dong P.,Soochow University of China | And 3 more authors.
Journal of Materials Chemistry B | Year: 2015

We demonstrate a strategy for effective radioprotection by chitosan-based long-circulating nanocarriers with radio-protective agents. The stable encapsulation does not restrain its radioprotective capability, and exhibits prolonged retention time in blood with a half-life of ∼10 h, thereby showing more beneficial effects than the pure agent in therapeutic efficacy for irradiated mice. © 2015 The Royal Society of Chemistry.

Qian J.,Soochow University of China | Zhang S.,Soochow University of China | Zhou Y.,Soochow University of China | Dong P.,Soochow University of China | And 2 more authors.
RSC Advances | Year: 2015

Uranium(VI) may pose a great threat to human health and the environment owing to its high chemical toxicity and radioactivity. A novel method is reported herein to synthesize surface ion-imprinted magnetic microspheres (SII-MM) for efficient removal of uranium(VI). Specifically, uranyl ion-imprinted polymer-functionalized Fe3O4@SiO2 microspheres were prepared by surface-locating copolymerization of N-hydroxyethylacrylamide and 1-vinylimidazole. The effects of chemical composition, pH, adsorbent dose, competing ions and initial concentration on the adsorption of uranyl ions were evaluated. The exothermic spontaneous adsorption kinetically followed a pseudo-second-order model, and the process of SII-MM could reach equilibrium with a capacity of 146.41 mg of U per g within 1.0 min at pH 5.0 and 298.15 K. Compared with non-imprinted composites, SII-MM showed higher selectivity, faster kinetics, and larger capacity for uranyl adsorption. This work indicates that the SII-MM can be used as a promising adsorbent to effectively remove uranium(VI) from aqueous solutions. © The Royal Society of Chemistry 2015.

Chen D.,Soochow University of China | Chen D.,Jiangsu Higher Education Institutions | Desmond K.W.,Emory University | Weeks E.R.,Emory University
Physical Review E - Statistical, Nonlinear, and Soft Matter Physics | Year: 2015

We experimentally study rearranging regions in slow athermal flow by observing the flow of a concentrated oil-in-water emulsion in a thin chamber with a constricting hopper shape. The gap of the chamber is smaller than the droplet diameters, so that the droplets are compressed into quasi-two-dimensional pancakes. We focus on localized rearrangements known as "T1 events" where four droplets exchange neighbors. Flowing droplets are deformed due to forces from neighboring droplets, and these deformations are decreased by nearby T1 events, with a spatial dependence related to the local structure. We see a tendency of the T1 events to occur in small clusters. © 2015 American Physical Society.

Sun Y.,North China Electrical Power University | Sun Y.,Jiangsu Higher Education Institutions | Yang S.,North China Electrical Power University | Chen Y.,Kyoto University | And 3 more authors.
Environmental Science and Technology | Year: 2015

The adsorption and desorption of U(VI) on graphene oxides (GOs), carboxylated GOs (HOOC-GOs), and reduced GOs (rGOs) were investigated by batch experiments, EXAFS technique, and computational theoretical calculations. Isothermal adsorptions showed that the adsorption capacities of U(VI) were GOs > HOOC-GOs > rGOs, whereas the desorbed amounts of U(VI) were rGOs > GOs > HOOC-GOs by desorption kinetics. According to EXAFS analysis, inner-sphere surface complexation dominated the adsorption of U(VI) on GOs and HOOC-GOs at pH 4.0, whereas outer-sphere surface complexation of U(VI) on rGO was observed at pH 4.0, which was consistent with surface complexation modeling. Based on the theoretical calculations, the binding energy of [G⋯UO2]2+ (8.1 kcal/mol) was significantly lower than those of [HOOC-GOs⋯UO2]2+ (12.1 kcal/mol) and [GOs-O⋯UO2]2+ (10.2 kcal/mol), suggesting the physisorption of UO22+ on rGOs. Such high binding energy of [GOs-COO⋯UO2]+ (50.5 kcal/mol) revealed that the desorption of U(VI) from the -COOH groups was much more difficult. This paper highlights the effect of the hydroxyl, epoxy, and carboxyl groups on the adsorption and desorption of U(VI), which plays an important role in designing GOs for the preconcentration and removal of radionuclides in environmental pollution cleanup applications. © 2015 American Chemical Society.

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