Determination of cadmium with a sequential injection lab-on-valve by anodic stripping voltammetry using a nafion coated bismuth film electrode

This work exploited a sequential injection lab-on-valve (LOV) system for the determination of cadmium by anodic stripping voltammetry (ASV). A miniaturized electrochemical flow cell (EFC) was fabricated in LOV, in which a nafion coated bismuth film electrode was used as working electrode. The cadmium was electrodeposited on the electrode surface in bismuth solution, and measured with the subsequential stripping scan. Under optimal conditions, the proposed system responded linearly to cadmium concentrations in a range 2.0-100.0 μg L⁻¹. The detection limit of this method was found to be 0.88 μg L⁻¹. By loading a sample volume of 800 μL, a sampling frequency of 22 determinations h⁻¹ was achieved. The repeatability expressed as relative standard derivation (R.S.D.) was 3.65% for 20 μg L⁻¹ cadmium (n = 11). The established method was applied to analysis of trace cadmium in environmental water samples and the spiked recoveries were satisfactory.     

Cyclized oligomer of tetracyanoquinodimethane-tetrathiafulvalene (TCNQ-TTF): a versatile macrocyclic molecule by DFT calculations

Journal of Inclusion Phenomena and Macrocyclic Chemistry - The combination of the electron donor and acceptor into a donor–acceptor system can transform the intermolecular charge transfer...     

电容法研究卵磷脂/氨基酸/H_2O胶束和囊泡体系

运用电容法研究卵磷脂/氨基酸/H2O胶束和囊泡体系结构与性质.卵磷脂的临界胶束浓度和囊泡生成浓度可由体系电容-卵磷脂浓度关系曲线求得.随着卵磷脂浓度增加,体系电容增加,卵磷脂由胶束形成囊泡.随着氨基酸浓度增加,胶束、囊泡半径增大,体系电容减小.氨基酸能促进卵磷脂形成胶束和囊泡,使得卵磷脂临界胶束浓度和囊泡生成浓度减小,其影响的强弱顺序为组氨酸色氨酸垌甘氨酸.     

Hierarchical 0D/2D Co3O4 hybrids rich in oxygen vacancies as catalysts towards styrene epoxidation reaction

Great efforts have been devoted to the developing of simple, efficient and stable heterogeneous catalysts for the styrene epoxidation reaction (SER). Metal oxides can be of industrial importance by offering an economic and green route for selectively converting styrene into styrene oxide (SO). Herein, by treating the pristine porous 2D Co₃O₄ sheets with NaBH₄ solution, a novel hierarchical structure, i.e., 0D Co₃O₄ nanoparticles decorated on 2D porous Co₃O₄ sheets, was obtained. This simple solution reduction strategy not only realizes the morphology evolution, but also induces the modification of the valence states of metal ions and the simultaneous generation of surface oxygen vacancies. The hierarchical 0D/2D Co₃O₄ hybrids rich in oxygen vacancies (OV-Co₃O₄) exhibit a much better SER performance than the Co₃O₄ sheets (P-Co₃O₄), with the yield of SO more than doubled. The excellent catalytic performance of the OV-Co₃O₄ can be ascribed to the synergistic effects regarding the hierarchical porous structure, the modification of surface chemical composition and the creation of surface oxygen vacancies.     

Differential Harnack inequalities for heat equations with potentials under geometric flows

In the paper we consider a closed Riemannian manifold M with a time-dependent Riemannian metric g _ij (t) evolving by ? _t g _ij  = ?2S _ij , where S _ij is a symmetric two-tensor on (M,g(t)). We prove some differential Harnack inequalities for positive solutions of heat equations with potentials on (M,g(t)). Some applications of these inequalities will be obtained.     

The effect of high-energy radiation on aqueous solution of Acid Red 1 textile dye

The effect of high-energy radiation on Acid Red 1 (AR1) azo-dye solution was investigated by UV–Vis spectroscopy and chemical oxygen demand (COD) measurements. Doses in the order of 10 kGy cause complete decolouration of the 10⁻³–10⁻⁴ mol dm⁻³ solutions; however, for complete mineralization doses higher by 1–2 order of magnitude are needed. Hydrated electrons and H atom are more effective in fading reaction, while the OH radicals have higher efficiency in mineralization. The HO₂^•/O₂^•− radical–radical anion pair is rather inefficient in fading reaction.     

Packing capilllary electrochromatography columns using vacuum--a preliminary study

This paper introducesa novel method for packing Capillary Electrochromatography Columns (CEC). Using vacuum packing methodology, silica particles as small as 1 microm were successfully packed into the capillary columns with 75 microm inner diameter. The columns are verystable and show no noticeable loss in efficiency after 200 sample injections. The performance of these vacuum packed capillary columns was evaluated with a mixture of aromatic and non-aromatic compounds. A 24 cm long capillary column can produce peak efficiencies of around 45,000 plates for benzene.