乙酰胺-氯化锌新型离子液体的合成及物化性质

合成了CH3CONH2-ZnCl2体系离子液体;利用红外光谱仪分析了CH3CONH2-ZnCl2离子液体的化学特征,采用步冷曲线法绘制了CH3CONH2-ZnCl2二元体系熔点图,测定了其物化性质.结果表明,CH3CONH2-ZnCl2二元体系的最低熔点为8℃;当CH3CONH2与ZnCl2的摩尔比为3:1时,Zn2+...     

Selective water sorbents for multiple applications, 8. sorption properties of CaCl2?SiO2 sol-gel composites

This paper presents sorption properties of CaCl₂/SiO₂ composites synthesized by a sol-gel approach. Desorption isobars measured at T=30–140°C and vapor pressure 12.8–81.0 mbar clearly show a correlation between the sorbents pore structure and their sorption properties. The sample adsorptivities are found to exceed 1.2 kg H₂O/kg adsorbent (or 20–25 mol H₂O/mol of the salt). That is markedly higher than any reported before for silica-based materials. This results in a high energy storage capacity reaching 3,400 kJ/kg of dry sorbent, as confirmed by direct calorimetric measurements. The isosteric desorption heat is found to decrease from 67±5 kJ/mol to 46±5 kJ/mol with increase in the surface coverage.     

The Effect of the Modification of Carbon Spheres with ZnCl2 on the Adsorption Properties towards CO2

Zinc chloride and potassium oxalate are often applied as activating agents for carbon materials. In this work, we present the preparation of ZnO/carbon spheres composites using resorcinol-formaldehyde resin as a carbon source in a solvothermal reactor heated with microwaves. Zinc chloride as a zinc oxide source and potassium oxalate as an activating agent were applied. The effect of their addition and preparation conditions on the adsorption properties towards carbon dioxide at 0 °C and 25 °C were investigated. Additionally, for all tested sorbents, the CO₂ sorption tests at 40 °C, carried out utilizing a thermobalance, confirmed the trend of sorption capacity measured at 0 and 25 °C. Furthermore, the sample activated using potassium oxalate and modified using zinc chloride (a carbon-to-zinc ratio equal to 10:1) displayed not only a high CO₂ adsorption capacity (2.69 mmol CO₂/g at 40 °C) but also exhibited a stable performance during the consecutive multicycle adsorption–desorption process.     

Research Progress on Typical Quaternary Ammonium Salt Polymers

Quaternary ammonium salt polymers, a kind of polyelectrolyte with a quaternary ammonium group, are widely used in traditional and emerging industries due to their good water-solubility, adjustable cationicity and molecular weight, high efficiency and nontoxicity. In this paper, firstly, the properties and several synthesis methods of typical quaternary ammonium salt monomers were introduced. Secondly, the research progress on the synthesis of polymers was summarized from the perspective of obtaining products with high molecular weight, narrow molecular weight distribution and high monomer conversion, and special functional polymers. Thirdly, the relationships between the structures and properties of the polymer were analyzed from the perspectives of molecular weight, charge density, structural stability, and microstructural regulation of the polymer chain unit. Fourthly, typical examples of quaternary ammonium salt polymers in the application fields of water treatment, daily chemicals, petroleum exploitation, papermaking, and textile printing and dyeing were listed. Finally, constructive suggestions were put forward on developing quaternary ammonium salt polymers with high molecular weights, strengthening the research on the relationships between the structures and their properties and pinpointing relevant application fields.     

氯化钾水溶液微观结构的分子动力学模拟研究

氯化钾水溶液不同于氯化钠的,其在低温下只能形成无水盐和冰.现有研究表明在氯化钠水溶液中不仅存在着水分子连续分布的区域与离子团簇,而且这二者的物质组成也与该溶液所形成晶体的分别对应.为了探寻其他溶液中是否存在此类对应关系,并考察溶液的微观结构,本文采用分子动力学方法对氯化钾水溶液进行了研究,表明了该溶液的一些性质.氯化钾水溶液中K⁺-K⁺和Cl^--Cl^-径向分布函数的特征具有一致性,峰的最大值所对应的位置都分别相同,明显不同于氯化钠水溶液的.系列时刻下瞬态图像内O到其最近离子距离中最大值的统计结果表明氯化钾水溶液中存在着一定大小的水分子连续分布的区域,其平均尺寸至少为2.26 nm;瞬态图像中K⁺与其最近邻Cl^-之间的距离主要分布在0.28 nm～0.38 nm之间,占比约为97.4%;溶液中存在着较大和较小两类离子团簇,较大团簇的平均尺寸为1.73nm,平均离子数是25.0,其内部的离子与周围离子之间具有与氯化钾晶体类似的结构;这些结果表明氯化钾水溶液中也...     

Effect of the End Groups and the Solvent on the Gelation of the Hybrid Materials from Poly (Vinyl Chloride) (PVC) and Oligo Phenylene Vinylene (OPV)

Abstract

The role of the end-groups of three oligophenylene vinylene (OPV) and the solvents on the hybrid materials from poly (vinyl chloride) (PVC) and the OPV are examined. The gelation of the three organogel OPVs and of the hybrid materials in bromobenzene and benzyl alcohol was characterized. The morphology, as well as the thermodynamic properties, of these OPV and hybrid materials showed that they depended mostly on the solvent and very little on the different end-groups located on the OPV backbones.     

Visible-Light-Induced Vicinal Dichlorination of Alkenes through LMCT Excitation of CuCl2

This work demonstrates photoredox vicinal dichlorination of alkenes, based on the homolysis of CuCl₂ in response to irradiation with visible light. This catalysis proceeds via a ligand to metal charge transfer process and provides an exciting opportunity for the synthesis of 1,2-dichloride compounds using an inexpensive, low-molecular-weight chlorine source. This new process exhibits a wide substrate scope, excellent functional group tolerance, extraordinarily mild conditions and does not require external ligands. Mechanistic studies show that the ready formation of chlorine atom radicals is responsible for the facile formation of C−Cl bonds in this synthetic process.     

Photo- and cathodoluminescence of the cetylpyridinium chloride: ZnO nanocomposites

The cathodoluminescence and photoluminescence (PL) spectra of ZnO nanoparticles (NPs) embedded into the cetylpyridinium chloride (CPCL) matrix were studied. The composites were obtained by drying an aqueous suspension of CPCL and ZnO NPs, with NaCl and with NaOH additives. We observed that only NaOH addition lead to a significant increase in the PL intensity which we attribute to the surface chemistry of the ZnO NPs. We propose that thin ZnOH₂ and Na₂ZnO₂ layers form on the surface of the NPs; these layers present an increased number of oxygen vacancies, which act as emitting centres.     

Dielectric studies of the phase transition in {N(CH3)4}2HgCl4

Dielectric properties of single-crystal {N(CH₃)₄}₂HgCl₄ (structure at room temperature; orthorhombic Pmcn) have been measured in a temperature range from 4 K to about 370 K. The dielectric constant along the a-, b-, and c-axes shows a break at 278 K. No other anomalies are detected in the temperature range studied. The transition temperature increases linearly with increasing hydrostatic pressure at a rate of 0.20 K/MPa. Twin boundaries are observed in the low-temperature phase on b-plate specimens. The results indicate that the phase transition in {N(CH₃)₄}₂HgCl₄ is ferroelastic, as in {N(CH₃)₄}₂XBr₄ (X: Mn, Co, Zn).     

毛细管电泳法分离联萘酚对映体

利用新的手性选择剂苄基氯化辛可宁，在非水相中成功地分离了联萘酚的对映体，并对分离的机理作了初步地探讨。