一种CO2的矿化封存新方法

针对目前CO2矿化封存的研究现状,提出了一种新的CO2矿化封存方法:利用CO2和NH3反应生成三聚氰酸固体,并考察了温度、压力、反应物配比及有无催化剂对三聚氰酸收率的影响。当反应条件为在250℃,22MPa,NH3与CO2反应配比为1∶1.4,反应8h时,最高收率可达到68.3%。此项技术能够与现在工业成熟的富氧燃烧技术联用,实现对CO2的永久性封存,具有经济效益。     

Study on sorption of U(VI) onto ordered mesoporous silicas

The mesoporous silicas (MCM-41 and MCM-48) are synthesized by hydrothermal method, which are characterized by XRD and BET techniques. The application of mesoporous silicas for the sorption of U(VI) from aqueous solution are studied by using batch technique under ambient condition. The effects of contact time, solid-to-liquid ratio (m/V), solution pH, ionic strength and temperature are determined, and the results indicate that the sorption of U(VI) to MCM-41 or MCM-48 are strongly dependent on pH values but independent of ionic strength. Compared with Langmuir model, the sorption isotherms can be simulated by Freundlich model well according to the high relative coefficients. The parameters for Langmuir and Freundlich sorption isotherms are calculated from the temperature at 298, 318 and 338 K, respectively, and the results suggest that the sorption of U(VI) on MCM-41 or MCM-48 is a spontaneous and exothermic process. In contrast to its sorption capacity for U(VI), MCM-48 is a suitable material for the preconcentration of U(VI) from large volumes of aqueous solutions.     

Preparation and characterization of nanosized TiO2 powder as an inorganic adsorbent for aqueous radionuclide Co(II) ions

In this research TiO₂ sample was synthesized by a simple sol–gel method and was characterized by X-ray diffraction (XRD), Transmission electron microscopy (TEM) and Brunauer–Emmett–Teller (BET) techniques. The XRD result indicated that the obtained product was anatase titanium dioxide with high purity, the TEM image clearly showed that the particle sizes of TiO₂ nanoparticles were in the range of 30–70 nm, and the measured BET surface area of the heated TiO₂ nanoparticles was 147.14 m²/g. In this work, the prepared TiO₂ sample was used as a new adsorbent for the adsorption of radionuclide Co(II) ions from aqueous solutions, and the influence of pH, contact time, ionic strength and temperature in the presence or absence of humic acid/fulvic acid (HA/FA) were also investigated. The experimental results indicated that the adsorption of Co(II) ions onto TiO₂ was strongly pH-dependent. Based on the surface complexation, the presence of HSs enhanced the adsorption of Co(II) ions and the influence of Co(II) adsorption onto FA–TiO₂ hybrids was much stronger than that of HA–TiO₂ at pH values of 2.0–9.0. Adsorption of Co(II) ions onto TiO₂ powder was strongly dependent on ionic strength. The adsorption process mainly occured in the first contact time of 2 h and could be fitted by a pseudo-second-order rate model. The calculated thermodynamic data indicated that the adsorption of Co(II) ions onto TiO₂ was a spontaneous process and favorable at high temperatures.     

Gold-nanoparticle on the surface of L-cysteine modified gold electrode and its application

A sensor based on gold nanoparticle on the surface of L-cysteine modified gold electrode is prepared. Electrochemical behavior of dopamine hydrochloride is investigated. The linear relation between peak current of dopamine hydrochloride and scan speed in the range of 10 to 1000 mV s^?1 indicates that a diffusion-adsorption controls the process. The linearity range is 1.05 × 10^?5–7.38 × 10^?4 M with detection limit of 1.05 × 10^?6 M. The recoveries were in the range from 99.8 to 101.5% with relative standard deviations of 1.3 ～ 2.3% (n = 6). The modified electrode under ambient conditions over a period of 2 weeks has an excellent repeatability and reproducibility.     

Synthesis of gold nanoparticles on the surface of pyrolytic graphite using penicillin as a stabilizing reagent and the catalytic oxidation of α-naphthylamine

Electrochemical synthesis of gold nanoparticles on the surface of pyrolytic graphite using penicillin as a stabilizing reagent was proposed. The gold nanoparticles were characterized by scanning electron microscopy, cyclic voltammetry, IR spectra, UV spectra, and powder X-ray diffraction spectra. The electro-chemical catalysis of penicillin for α-naphthylamine was demonstrated.     

以羧酸作为酰化剂的酰化反应及其在有机合成中的应用

传统的傅-克酰基化反应以酰氯或酸酐作为酰化剂、路易斯酸作为催化剂。大量路易斯酸催化剂及反应产生的氯化氢都需要后处理,并且酰氯对湿度敏感,储存及使用过程中易发生危险。而以三氟乙酸酐作为活化剂、直接以羧酸作为酰化剂的酰化反应不需要事先将羧酸制成酰氯、酸酐或酰胺,且活化剂三氟乙酸酐及副产物三氟乙酸都能很容易地通过蒸馏回收,因此,这类酰化反应能有效解决传统的傅-克酰基化反应所存在的问题。本文综述了近20年来以三氟乙酸酐作为活化剂、直接以羧酸作为酰化剂的酰化反应方法的发展,以及其在功能有机分子、药物分子和天然产物合成中的应用。     

Binding and cytotoxicity of 131I-labeled gastrin-releasing peptide receptor antagonists modified by cell penetrating peptides

Gastrin releasing peptide receptors (GRPRs) are one of the most interesting targets over expressed in various tumors. Due to the superior potential of the GRPR antagonist analogs, they have been studied in the tumor radio imaging and therapy field. However, typical antagonists suffered the shortcomings of no internalization and poor binding affinity which hampered their applications in radiotherapy. Therefore, we attempted to introduce Oligoarginines (cell penetrating peptides) to RM26, aiming to increase the binding affinity or even trigger the internalization of the peptides on cells. The results showed Arg₆ as the most potent CPP, significantly enhanced the binding avidity of RM26 to the GRPR.

     

Modular Design of Noble‐Metal‐Free Mixed Metal Oxide Electrocatalysts for Complete Water Splitting

Electrocatalytic water splitting into H₂ and O₂ is a key technology for carbon‐neutral energy. Here, we report a modular materials design leading to noble metal‐free composite electrocatalysts, which combine high electrical conductivity, high OER and HER reactivity and high durability. The scalable bottom‐up fabrication allows the stable deposition of mixed metal oxide nanostructures with different functionalities on copper foam electrodes. The composite catalyst shows sustained OER and HER activity in 0.1 m aqueous KOH over prolonged periods (t>10 h) at low overpotentials (OER: ≈300 mV; HER: ≈100 mV) and high faradaic efficiencies (OER: ≈100 %, HER: ≈98 %). The new synthetic concept will enable the development of multifunctional, mixed metal oxide composites as high‐performance electrocatalysts for challenging energy conversion and storage reactions.     

Separation,Quantification and Structural Study of (+)‐Catechin and (–)‐Epicatechin by Ion Mobility Mass Spectrometry Combined with Theoretical Algorithms

Two catechin epimers and their non‐covalent complexes with γ‐cyclodextrin were studied by using ion mobility coupled with mass spectrometry (IM‐MS). Rapid separation of complexes was achieved with the peak‐to‐peak resolution reaching 0.86 after optimization of IM condition. Collision cross section (CCS) was measured to explore the structural difference of complexes. A gap of 11.75 Ų between two complexes was found. Molecular modeling and theoretical CCS calculation were adopted to explain the measurement results. Two binding ways of both complexes were found and the calculated CCS corresponds accurately to the measured CCS. Quantification of catechins in mixtures was performed and the relative error was less than 15%, indicating the effectiveness of quantification by IM‐MS.     

Comparative pharmacokinetic study of four major bioactive components after oral administration of Zhi‐Zi‐Hou‐Po decoction in normal and corticosterone‐induced depressive rats

A highly selective and efficient LC–MS/MS method was developed to determine the plasma concentration of magnolol, hesperidin, neohesperidin and geniposide following oral administration of Zhi‐Zi‐Hou‐Po decoction in normal and depressed rats. Plasma samples were pretreated by protein precipitation with methanol. Chromatographic separation was performed on an XTerra^® MS C₁₈ column using a gradient elution with a mobile phase composed of acetonitrile–0.1% aqueous formic acid. The proposed method was validated to be specific, accurate and precise for the analytes determination in plasma samples. The calibration curves displayed good linearity over definite concentration ranges for the analytes. The intra‐ and inter‐day precision of the proposed method at three different levels were all within <11.13% and the relative errors ranged from ?8.46 to 8.93%. The recovery of the four compounds ranged from 82.72 to 89.08% and no apparent matrix effect was observed during sample analysis. After full validation, the established method was successfully applied for comparing the pharmacokinetics of four components between normal and depressed rats. The results showed that the AUC and C_max of four analytes in depressed rats were significantly different from those in normal rats and might provide helpful information to guide the clinical use of Zhi‐Zi‐Hou‐Po to treat depression.