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A series of mesoporous Ni–Cu/WO3/ZrO2 (1Ni1Cu/mWZr) was successfully prepared with F127 as a template and used as catalysts for isobutane hydroisomerization to n-butane. The effects of the F127/ZrO...

Electrochemical CO2 reduction is considered as a promising strategy for CO2 conversion and utilization. However, developing efficient and low-cost electrocatalysts still remains a great challenge. Herein, Ni–N@NPC was prepared using tobacco stem derived nitrogen-containing porous carbon (NPC) as a support and 1,10 phenanthroline as a chelating agent, as well as nickel(II) acetate tetrahydrate as a Ni source. The prepared Ni–N@NPC has highly dispersed Ni–N sites and good CO2 adsorption capacity. Ni–N@NPC exhibits excellent electrochemical CO2 reduction property, including high faradaic efficiency for CO (about 98.44%) at a medium overpotential of 670 mV and high activity (current density approximately 30.96 mA cm−2), as well as durable stability over 30 hours. In addition, the Ni–N@NPC still maintains a Faraday efficiency over 90.5% at wide potentials (from −0.57 V to −0.87 V). DFT calculation reveals that Ni–N sites decrease the kinetic energy barriers for *CO2 transition to *COOH, indicating that the high electrochemical CO2 reduction activity is attributed to the Ni–N sites in electrocatalysts. This work provides a new way to develop biomass carbon materials and promote their application in energy conversion.

This work presents a simple and straightforward approach to fabricating multifunctional nanocomposite particles which possess a core of a polystyrene (PS) particle, a transition layer of magnetic Fe3O4 nanoparticles (NPs), and an outer shell of adsorbable polyaniline (PANi). In detail, the positively charged Fe3O4 NPs synthesized via the chemical co-precipitation method are directly loaded onto the negatively charged surfaces of the PS particles obtained by emulsifier-free emulsion polymerization through electrostatic self-assembly; subsequently, the coating of the resultant PS/Fe3O4 nanocomposite particles with PANi was successfully achieved by virtue of the “swelling–diffusion–interfacial-polymerization method” (SDIPM). Furthermore, the adsorption of Cu2+ by PS/Fe3O4@PANi nanocomposite particles was investigated by changing the initial pH value, adsorption time, and initial concentration of the adsorbate. The adsorption data in our work follow a pseudo-second-order kinetics model and fit the Langmuir isotherm model. The PS/Fe3O4@PANi nanocomposite particles show that the maximum adsorption capacity is up to 181.5 mg g−1 at pH 5. More importantly, these nanocomposite particles can be easily recovered using an external magnetic field owing to the presence of Fe3O4 NPs, and the regenerated nanocomposite particles can be repeatedly used for eight cycles without significant loss of their adsorption capacity.

Herein an in situ growth of clean palladium nanoparticles (Pd NPs) on functional reduced graphene oxide (RGO)-coated polystyrene (PS) microspheres is achieved by a simple two-step process. On the basis of the hydrophobic interaction and π-electron interaction, the PS/RGO composite particles are first prepared by the reduction of graphene oxide in the presence of PS microspheres. Second, without using any additional reducing agent or stabilizer, the clean Pd NPs grow in situ on the surface of PS/RGO composite particles in water through a spontaneous redox reaction between Pd2+ and RGO. Significantly, owing to the stabilizer-free surface of Pd NPs and the synergistic effect of RGO and Pd NPs, the resultant PS/RGO@Pd composite particles feature pronounced catalytic activity toward the reduction of p-nitrophenol and Suzuki coupling reactions. Moreover, the catalyst particles can be easily recovered by centrifugation because of the large size of support microspheres and recycled consecutively.

BACKGROUND As an environmentally benign particle emulsifier, starch nanocrystal (SNC) has attracted considerable attention. By submitting waxy maize starch to acid below the gelatinisation temperature of starch, nanoscale crystalline residues, which are SNCs, were separated from starch granules by hydrolysing amorphous regions. The SNC could be used as a particle emulsifier to stabilise emulsions. RESULTS The SNC could adsorb at the oil–water interface to stabilise oil-in-water emulsions with high stability to coalescence. The creaming of emulsions occurred after homogenisation but decreased with increasing SNC content, which was mainly due to the formation of an inter-particle network in the emulsions. Because of the amount of sulfuric groups at the surface, the SNC was negatively charged. Therefore, at low pH values or high salt content the electrostatic repulsion of the SNC was reduced, which further caused droplet aggregation and an increase in size of the particles in the emulsions stabilised by the SNC. CONCLUSION The SNC was an efficient particle emulsifier for preparing Pickering emulsions. The size of emulsions stabilised by the SNC could be tailored by changing the pH value or salt concentration. © 2013 Society of Chemical Industry

The surface properties of native starch, namely rice, waxy maize, wheat and potato starch were characterized by contact angle measurement, zeta-potential, and then the emulsifying ability of these native starch granules was investigated by using liquid paraffin as oil phase and starch granules as sole emulsifier. It was found that emulsions could be prepared by using rice, waxy maize and wheat starch granules as emulsifier, but not potato starch, which had no emulsifying ability even when the concentration of starch granules as high as 15 wt% relative to water phase. Rice starch was the best emulsifier among these native starches. The emulsion stabilized by rice granules proved to be stable to coalescence for several months when the starch concentration was above 3 wt% relative to water phase. With the increasing of the rice starch concentration, the sizes of droplets decreased and the stability of emulsions enhanced. The salt and pH values had no significant influence on the packing structure of native starch granules at interface.

Waxy maize starch was hydrolyzed with sulfuric acid in aqueous solution. The remaining starch granules after acid hydrolysis were characterized by TEM and wide-angle XRD. Starch nanocrystals with size between 40 to 80 nm and relative crystallinity of 63% were obtained after 6 days of hydrolysis. Starch nanocrystals/carboxymethyl chitosan composite films were prepared by casting-evaporation method. When the starch nanocrystals content was below 30 wt%, the filler dispersed uniformly in the carboxymethyl chitosan matrix, whereas aggregation of starch nanocrystals and phase separation between aggregates and matrix were observed when the starch nanocrystals content was higher than 30 wt%. The maximum tensile strength (TS) of composite films approached ∼29 MPa, which was two times higher than that of the carboxymethyl chitosan film without filling starch nanocrystals. The percentage elongation at break (EB%) of nanocomposite films decreased with the increasing of the starch nanocrystals content. The water absorption and water vapor barrier property of carboxymethyl chitosan film were significantly improved by adding starch nanocrystals.

Trimethylsilylated hydroxyethyl cellulose (TMSHEC) was synthesized by using hexamethyldisilazane (HMDS) as silylated agent. With the partial protection of hydroxyl groups of HEC by silylation, the novel poly(ɛ-polycaprolactone) (PCL) grafted HEC (HEC-g-PCL) copolymers were successfully prepared by homogenous ring-opening graft polymerization and deprotection procedure. The structure of HEC-g-PCL copolymers was characterized by FTIR and 1H NMR. Fluorescence spectrum of HEC-g-PCL copolymer dilute solution indicated that copolymers could associate and form hydrophobic microdomains in aqueous solution. With the increasing of grafted PCL content, the critical association concentration (cac) of HEC-g-PCL copolymers decreased. The surface tension of HEC-g-PCL copolymers decreased dramatically with the increasing of the concentration and then approached to a plateau value when concentration was above the cac of HEC-g-PCL copolymers. The hydrodynamic radius of the aggregate of copolymer in dilute solution was found to increase with the increasing of the grafted PCL content. When the concentration of copolymer was above the cac, the zero-shear viscosity of the copolymer increased sharply and became much higher than that of HEC at the same concentration.