Novel mesoporous Si@C microspheres as anodes for lithium-ion batteries.

In this paper, we demonstrate the design and synthesis of novel mesoporous Si@C microspheres as anode materials for high-performance lithium-ion batteries. SiO2 nanoparticles modified with hexadecyl trimethyl ammonium bromide are enveloped within resorcinol-formaldehyde polymer microspheres which form in the ethanol-water-ammonia system. Mesoporous voids between Si nanoparticles and the carbon framework are generated after carbonization at 800 °C and magnesiothermic reduction at 650 °C. The resultant Si@C microspheres show regular spherical shapes with a mean diameter of about 500 nm, a mesopore size of 3.2 nm and specific surface areas of 401-424 m(2) g(-1). Mesoporosity of Si@C microspheres effectively buffers the volume expansion/shrinkage of Si nanoparticles during Li ion insertion/extraction, which endows mesoporous Si@C microspheres with excellent electrochemical performance and cycle stability when they are used as lithium-ion battery anode materials. A typical sample of mesoporous Si@C microspheres presents a specific capacity of 1637 and 1375 mA h g(-1) at first discharge and charge under a current density of 50 mA g(-1). After 100 cycles, the charge capacity remains 1053 mA h g(-1) with a coulombic efficiency of 99%, showing good cycle stability of the anode. This finding highlights the potential application of mesoporous Si@C microspheres in lithium-ion battery anode materials.

A seeded synthetic strategy for uniform polymer and carbon nanospheres with tunable sizes for high performance electrochemical energy storage.

We established a novel and facile strategy to synthesize uniform polymer and carbon nanospheres, the diameters of which can be precisely programmed between 35-105 and 30-90 nm, respectively, via time-controlled formation of colloidal seeds. The carbon nanospheres show promising prospects in high rate performance electrochemical energy storage.

Supramolecular core-shell nanosilica@liposome nanocapsules for drug delivery.

The fabrication of core-shell structural nanosilica@liposome nanocapsules as a drug delivery vehicle is reported. SiO(2) nanoparticles are encapsulated within liposomes by a W/O/W emulsion approach to form supramolecular assemblies with a core of colloidal particles enveloped by a lipid bilayer shell. A nanosilica core provides charge compensation and architectural support for the lipid bilayer, which significantly improves their physical stability. A preliminary application of these core-shell nanocapsules for hemoglobin (Hb) delivery is described. Through the H-bonding interaction between the hydroxyl groups on nanosilicas and the amino nitrogens of Hb, Hb-SiO(2) nanocomplexes in which the saturated adsorption amount of Hb on SiO(2) is 0.47 g g(-1) are coated with lipids to generate core-shell Hb-SiO(2)@liposome nanocapsules with mean diameters of 60-500 nm and Hb encapsulation efficiency of 48.4-87.9%. Hb-SiO(2)@liposome supramolecular nanovehicles create a mode of delivery that stabilizes the encapsulated Hb and achieves long-lasting release, thereby improving the efficacy of the drug. Compared with liposome-encapsulated Hb and Hb-loaded SiO(2) particles, such core-shell nanovehicles show substantially enhanced release performance of Hb in vitro. This finding opens up a new window of liposome-based formulations as drug delivery nanovehicles for widespread pharmaceutical applications.

A novel liposome-encapsulated hemoglobin/silica nanoparticle as an oxygen carrier.

A novel liposome-encapsulated hemoglobin/silica nanoparticle (LEHSN) was fabricated by a water-in-oil-in-water (W/O/W) double emulsion approach. Bovine hemoglobin (Hb) was first adsorbed onto the surfaces of silica nanoparticles (SNs), and then the complex of Hb/SNs was encapsulated by liposome to form LEHSN which has a core-shell supramolecular structure. On the one hand, liposomes built a cell membrane-like environment for the controlled release of Hb. On the other hand, SNs which act as rigid core provide a supported framework for lecithin membrane, and enhance the stability of liposomes. In comparison with liposome-encapsulated Hb (LEH), LEHSN shows substantially enhanced stability and improved release property of Hb in vitro. This study highlights the potential of the novel LEHSN as an oxygen carrier for pharmaceutical applications.

[Determination of trace lead and iron in nickel chloride and manganese sulfate by flame atomic absorption spectrometry after coprecipitation with yttrium phosphate].

Using yttrium phosphate as the coprecipitation collector for the separation and preconcentration of trace lead and iron in nickel chloride and manganese sulfate, flame atomic absorption spectrometric (FAAS) determination was described in the present paper. Coprecipitation parameters including the pH of the solution, and the amounts of YCl3 and H3 PO4 were discussed. It was found that lead and iron in nickel chloride could be coprecipitated quantitatively in the range of pH 3.0-4.0, and so could be lead in manganese sulfate. The detection limits (3sigma) of lead and iron in 20 mL solution were 1.63 x 10(-2) mg x L(-1) and 4.58 x 10(-2) mg x L(-1) respectively. In NiCl2 solution the standard addition recoveries for lead and iron were 100.91% and 99.73% respectively, and in MnSO4 solution the standard addition recoveries were 99.45% and 98.98% respectively. The method has eliminated the interference of matrix, and the result is satisfied.

[Determination of trace copper and cadmium in water by flame atomic absorption spectrometry coupled with flow injection on-line preconcentration using air segmentation].

The flow injection on-line preconcentration with a knotted reactor (KR) system for the determination of copper and cadmium in water by flame atomic absorption spectrometry (FAAS) was described in the present paper. The precipitation preconcentration of trace copper and cadmium was achieved by on-line merging of the sample and ammonia solutions. The resultant precipitates were on-line collected by a knotted reactor (KR) without filtration, and then the authors used a process of air segmentation. A solution of 1 mol x L(-1) HNO3 was employed to dissolve the collected precipitates and to deliver the analyte into the FAAS system for on-line detection. With a sample loading flow rate of 4.4 mL x min(-1) and a preconcentration time of 90 s, the enhancement factor was 34 (for Cu) and 36 (for Cd) as compared with the conventional FAAS method. The detection limits (3sigma) are found to be 1.9 and 0.3 microg x L(-1) for copper and cadmium respectively. The precision (RSD, n = 11) was found to be 2.3% at the level of 30.0 microg x L(-1) of Cu (II), and 2.6% at the level of 20.0 microg x L(-1) of Cd (II). The proposed method has been successfully applied to the determination of Cu (II) and Cd (II) in water samples.

[Application of internal standardization to rapid coprecipitation technique using APDC-Cu(II) for FAAS determination of lead in salt].

A method was proposed for the determination of trace lead in salt with flame atomic absorption spectrometry after preconcentration of lead by rapid coprecipitation technique with APDC-Cu(II) using nickel as an internal standard at pH 2.5. The standard addition recovery of lead is between 92%-101%. The detection limit is 3.27 x 10(-3) microg x mL(-1) when the sample volume is 100 mL. The effect of matrix can be overcome by the method, and the results are satisfying. The method proposed here is rapid and has good reproducibility.