Enhanced Solar-Driven-Heating and Tough Hydrogel Electrolyte by Photothermal Effect and Hofmeister Effect.

Although plenty of progress and achievements are made on hydrogel electrolyte researches, the inherent inferior low-temperature performance of hydrogel electrolyte is still a severe challenge for wider application on the energy storage devices, due to the high content of water within hydrogel. Herein, an enhanced solar-driven-heating composite hydrogel electrolyte and a solar-driven-heating graphene based micro-supercapacitor are developed utilizing the photothermal conversion ability and self-initiation of MoS2 nanosheets and additional Hofmeister effect. The MoS2 composite hydrogel electrolyte not only improves the reliability of micro-supercapacitor owing to its splendid mechanical properties, but also endows the micro-supercapacitor with superior low-temperature electrochemical performance and broadens its operating environment to a much lower temperature (-56 °C), which should be attributed to the excellent ability in converting endless solar energy into required thermal energy. These efforts would construct a new application platform for solar energy conversion and present an efficient method to structure severe-cold resistant solid state energy storage devices for next-generation.

In Situ Fabrication of Benzoquinone Crystal Layer on the Surface of Nest-Structural Ionohydrogel for Flexible "All-in-One" Supercapattery.

Flexible energy-storage devices lay the foundation for a convenient, advanced, fossil fuel-free society. However, the fabrication of flexible energy-storage devices remains a tremendous challenge due to the intrinsic dissimilarities between electrode and electrolyte. In this study, a strategy is proposed for fabricating a flexible electrode and electrolyte entirely inside a matrix. First, a nest-structural and redox-active ionohydrogel with excellent stretchability (up to 3000%) and conductivity (167.9 mS cm-1 ) is designed using a hydrated ionic liquid (HIL) solvent and chemical foaming strategy. The nest-structure ionohydrogel provides sufficient "highways" and "service area", and the cation in HIL facilitates the reaction, transportation, and deposition of benzoquinone. Subsequently, in situ, a novel benzoquinone crystal-gel interface (CGI) is in situ fabricated on the surface of the ionohydrogel through electrochemical deposition of benzoquinone. Thus, an integrated CGI-gel platform is successfully achieved with a middle body as an electrolyte and the surficial redox-active CGI membrane for electrochemical energy conversion and storage. Based on the CGI-gel platform, an extreme simple and effective "stick-to-use" strategy is proposed for constructing flexible energy-storage devices and then a series of flexible supercapatteries are fabricated with high stretchability and capacitance (5222.1 mF cm-2 at 600% strain), low self-discharge and interfacial resistance and a wearable, self-power and intelligent display.

The sorption performance of corroded Gaomiaozi bentonite by evolved cement water at different temperatures: the case of europium removal.

In the Chinese high-level radioactive waste geological disposal program, Gaomiaozi (GMZ) bentonite has been selected as the potential buffer/backfill material. After the closure of the repository, the Ca-OH-type alkaline solution (evolved cement water) released by cement degradation may last for more than 100,000 years. The bentonite will undergo the corrosion of evolved cement water (ECW) for a long period. This work focuses on the sorption property of GMZ bentonite altered by ECW. Firstly, the corrosion experiments on compacted GMZ specimens with the dry density of 1.70 Mg/m3 were carried out under constant volume conditions at two temperatures. Then, the sorption of europium (Eu (III)) onto the corroded GMZ bentonite was studied by batch experiments. The results of batch sorption tests indicate that the altered GMZ bentonite keeps an effective removal property with the uptake of Eu (III) more than 99%. The effect of high-temperature conditions of the repository on the sorption property of bentonite is not significant. The results also suggest that the evolved cement water presents no detrimental effect on the long-term adsorption performance of bentonite even under higher temperature conditions.

Humidity-sensitive polymer xerogel actuators prepared by biaxial pre-stretching and drying.

This communication provides a facile approach to prepare a polyacrylamide polymer xerogel film which exhibits humidity-sensitive actuation and ionic conductivity.

Gum Arabic: A promising candidate for the construction of physical hydrogels exhibiting highly stretchable, self-healing and tensility reinforcing performances.

The preparation of tough and healable hydrogels in one step remains a big challenge throughout the field of hydrogel methodology. Herein, we fabricated a series of Poly(N,N-dimethyl acrylamide)-TiO2-gum arabic (PDMAA-TiO2-GA) hybrid hydrogels by simply introducing nanoparticles TiO2 and vinyl-modified gum arabic (GMAGA) into polymer networks. Without complicate molecular design and post-treating process, the hydrogel molding process was simple and effective. The hydrogel exhibited highly stretchable, self-healing and tensility reinforcing performances with the optimized compositions of 30% DMAA, 0.6% GMAGA and 0.13% TiO2. The maximum elongation of the hydrogel after self-healing recover could reach nearly 700% after only 20min healing time. The hydrogel could ensure 20 times continuous compressive or tensile tests without obvious deformation. Amazing was the significantly enhanced tensile modulus from 5kPa to 40kPa after 20 stretch-release cycles. The facile preparation and fascinating tensility reinforcing performance benefit the potential application of the carbohydrate GA in hydrogels.

Oxidoreductase-Initiated Radical Polymerizations to Design Hydrogels and Micro/Nanogels: Mechanism, Molding, and Applications.

Due to their 3D cross-linked networks and tunable physicochemical properties, polymer hydrogels with different sizes are applied widely in tissue engineering, drug-delivery systems, pollution regulation, ionic conducting electrolytes, agricultural drought-resistance, cosmetics, and the food industry. Novel, environmentally friendly, and efficient oxidoreductase-initiated radical polymerizations to design hydrogels and micro/nanogels have gained increasing attention. Herein, the recent advances on the use of novel enzyme-initiated systems for hydrogel polymerization, including the mechanisms, and molding of polymeric and hybrid-polymeric networks are reviewed. Preliminary progress related to interfacial enzymatic polymerization for the generation of hybrid micro/nanogels is introduced as an emerging initiating approach. In addition, certain biological applications in tissue engineering, bioimaging, and therapy are demonstrated step by step. Finally, some perspectives on the safety profile of enzymatic formed hydrogels, new enzymatic systems, and potential theranostic applications are discussed.

Oxygen-tuned nanozyme polymerization for the preparation of hydrogels with printable and antibacterial properties.

Nanozymes merge nanotechnology with biology and provide a lower cost and higher stability options, compared to that of natural enzymes. However, nanozyme catalyzed polymerization under physiological conditions is still a big challenge due to heavy oxygen inhibition. In this study, the simple glucose oxidase system can effectively adjust oxygen concentration and generate hydrogen peroxide, which assists in the realization of nanozyme-catalyzed polymerization. The nanozyme based hydrogel is printable due to its mild preparation with gradually increased viscosity. The antibacterial performance is ascribed to the in situ generated hydroxyl radical via the reaction of the bound nanozyme and glucose.

Interfacial behavior of Cyanex 302 and kinetics of lanthanum extraction.

In this paper, interfacial tension of Cyanex 302 is measured by a Sigma-701 tensiometer and the adsorption parameters are calculated according to the Gibbs and Szyszkowski adsorption isotherms. The interfacial adsorbed behavior of Cyanex 302 is investigated. The results demonstrate that the dimer is the predominant species in the bulk organic phase; however, the monomer is adsorbed at the interface and more interfacially active. The effects of aqueous pH, ion strength, and temperature on the interfacial activity of Cyanex 302 in heptane are discussed and explained in detail. The lower interfacial activity of Cyanex 302 in aromatic hydrocarbon than in aliphatic hydrocarbon has also been determined. The values of interfacial excess at the saturated interface increase in the order n-heptane>cyclohexane>toluene>benzene, which is consistent with the order of extractability of lanthanum by Cyanex 302 in these diluents. The interfacial activity data are used to discuss the kinetic mechanism of lanthanum(III) extraction. It is shown that an interfacial mechanism is very probable, and the extraction limiting step is the reaction between the Cyanex 302 molecules in the organic phase sublayer and the adsorbed intermediate complex.

Functional elastic hydrogel as recyclable membrane for the adsorption and degradation of methylene blue.

Developing the application of high-strength hydrogels has gained much attention in the fields of medical, pharmacy, and pollutant removal due to their versatility and stimulus-responsive properties. In this presentation, a high-strength freestanding elastic hydrogel membrane was constructed by clay nanosheets, N, N-dimethylacrylamide and 2-acrylamide-2-methylpropanesulfonic acid for adsorption of methylene blue and heavy metal ions. The maximum values of elongation and Young's modulus for 0.5% AMPSNa hydrogel were 1901% and 949.4 kPa, respectively, much higher than those of traditional hydrogels. The adsorptions were confirmed to follow pseudo-second kinetic equation and Langmuir isotherm model fits the data well. The maximum adsorption capacity of hydrogel towards methylene blue was 434.8 mg g(-1). The hydrogel also exhibited higher separation selectivity to Pb(2+) than Cu(2+). The methylene blue adsorbed onto the hydrogel membrane can be photocatalytically degraded by Fenton agent and the hydrogel membrane could be recycled at least five times without obvious loss in mechanical properties. In conclusion, this presentation demonstrates a convenient strategy to prepare tough and elastic clay nanocomposite hydrogel, which can not only be applied as recyclable membrane for the photocatalytic degradation of organic dye, but also for the recovery of valuables.

Magnetic nanocomposite hydrogel prepared by ZnO-initiated photopolymerization for La (III) adsorption.

Here, we provide an effective method to fabricate magnetic ZnO clay nanocomposite hydrogel via the photopolymerization. The inorganic components endow the hydrogel with high mechanical strength, while the organic copolymers exhibit good adsorption capacity and separation selectivity to La (III) ions. An optimized hydrogel has the maximum compressive stress of 316.60±15.83 kPa, which still exhibits 138.98±7.32 kPa compressive strength after swelling. The maximum adsorption capacity of La ion is 58.8 mg/g. The adsorption matches the pseudo-second-order kinetics model. La (III) ions can be effectively separated from the mixtures of La/Ni, La/Co, La/Cu, and La/Nd in a broad pH range (2.0 to 8.0). After six adsorption-desorption cycles, the hydrogel can maintain its adsorption capacity. This work not only provides a new approach to the synthesis of tough hydrogels under irradiation, but also opens up enormous opportunities to make full use of magnetic nanocomposite hydrogels in environmental fields.

Adsorption of lanthanum (III) from aqueous solution using 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester-grafted magnetic silica nanocomposites.

In view of increasing attention of magnetic materials in the field of separation science and technology, we provide an effective route for fabrication of a new magnetic material with high adsorption capacity and selectivity toward metal ions, excellent acid resistance property and long service life. Silica was firstly coated on the magnetic particles, and then silane-coupling agent (3-chloropropyltryethosysilane) was used for grating 2-ethylhexyl phosphonic acid mono-2-ethylhexyl (P507), an organophosphorous acid extractant, on the surface of magnetic silica nanocomposite. The amount of P507 anchored on the particle was estimated to be 0.43 mmol/g. The P507-grafted magnetic silica nanocomposite was stable over pH range of 0-14. The maximum adsorption capacity of La (III) was 55.9 mg/g at the optimized pH 5.5. The adsorption of La (III) on our nanocomposites was found to follow the second order kinetics equation and fit Langmuir isotherm model well. The PO functional groups took an important role in the coordination and adsorption mechanism, which was confirmed by FTIR and XPS techniques. After 10 adsorption/desorption cycles, no obvious decrease in adsorption capacity or obvious loss in saturation magnetization were observed.

Selective adsorption of molybdenum(VI) from Mo-Re bearing effluent by chemically modified astringent persimmon.

Astringent persimmon was chemically cross-linked by formaldehyde to obtain a novel kind of adsorption gel, which was named as APF gel. The adsorption behaviors of Mo(VI) and Re(VII) along with other coexisting metals onto the APF gel were studied in the present paper. The APF gel was found to be effective for the adsorption of Mo(VI) while the gel is almost completely inert toward rhenium and calcium over the whole hydrochloric acid concentration region. The APF gel has a low affinity for iron, copper, lead, nickel, manganese and zinc ions when the concentration of HCl is higher than 1 mol/L. The gel exhibited selectivity only for Mo(VI) with a remarkably high adsorption capacity 1.05 mol/kg, and the adsorption behavior obeys the Langmuir model. According to the thermodynamic and kinetic studies, the endothermic adsorption process followed pseudo-second order kinetics. Also, its excellent adsorption characteristics for Mo(VI) were confirmed by the adsorption and elution tests using a column packed with the APF gel. The result provides a new approach for the recovery of Mo(VI) from a industrial waste effluent.