化学转化法制备磁性阳离子交换树脂的研究

本文通过化学转化法即化学共沉淀法，分别研究了强酸性和弱酸性阳离子交换树脂的磁转化对相应所得树脂的磁性的影响，制得了磁性毫米级和微米级粒径的强酸性，弱酸性阳离子交换树脂。所得磁性树脂有磁性强，磁性物质分布均匀而且稳定，并保持树脂的原有特性。     

聚环卤代苯乙烯-二乙烯苯强酸性阳离子交换树脂的热稳定性

合成了一系列聚邻、间、对位卤代苯乙烯-二乙烯基苯强酸性阳离子交换树脂,研究了树脂在170℃水中的磺酸基热降解规律.结果表明,树脂的热稳定性次序为对氯苯乙烯树脂＞对溴苯乙烯树脂＞对氟苯乙烯树脂;邻氯苯乙烯树脂＞对氯苯乙烯树脂＞间氯苯乙烯树脂;邻氯苯乙烯树脂100h热降解率小于14.0%,降解速率为0.0028%/h,其热稳定性为最好.     

Denatured Thermodynamics of Proteins in Weak Cation－exchange Chromatography

The thermostability of some proteins in weak cation-exchange chromatography was investigated at 20—80 ℃. The results show that there is a fixed thermal denaturation transition temperature for each protein. The appearance of the thermal transition temperature indicates that the conformations of the proteins are de-stroyed seriously. The thermal behavior of the proteins in weak cation-exchange and hydrophobic interaction chromatographies were compared in a wide temperature range. It was found that the proteins have a higher thermostability in a weak cation-exchange chromatography system. The thermodynamic parameters (△H^0,△S^0) of those proteins were determined by means of Van′t t Hoff re|ationship(lnk′-1/T). According to stan-dard entropy change(△S^0) , the conformational change of the proteins was judged in the chromatographic pro-cess. The linear relationships between △H^0 and △S^0 can be used to evaluate “compensation temperature“ (β) at the protein denaturation and identify the identity of the protein retention mechanism in weak cation-ex-change chromatography.     

Optimization strategies for off-line two-dimensional liquid chromatography

A step by step strategy of optimization of comprehensive off-line two-dimensional liquid chromatography (2D-LC) separations is proposed. The goal of an optimization process in the separation sciences is either to achieve a given resolution (a target peak capacity in 2D-LC) within as short a time as possible or to reach the highest possible resolution in a given analysis time. The proposed method takes into account the characteristics of the columns used in the first and the second dimension and the number of fractions of the first dimension eluent that should be collected. The effect of the time spent during the analysis on the second dimension column to carry out necessary tasks that are not the separation itself (called the additional time) on the maximum peak capacity that is achievable was carefully investigated. It was shown that (1) an increase in the peak capacity of the first dimension column combined with the collection of larger volume fractions permits a significant reduction of the time needed to achieve the desired peak capacity; and (2) there is an optimum fraction collection ratio (or number of collected fractions per peak) which yields the target peak capacity in the minimum time. The proposed strategy was used for the optimization of the separation of samples of BSA tryptic digest by an off-line 2D-LC using an SCX⊗RP$\text{SCX}\otimes \text{RP}$-HPLC method. As a result of this optimization, a peak capacity of 4000 could be achieved in about 5 h with the two columns available. The time needed for the optimized analysis was less than two thirds of the analysis time that would have been needed had the conventional rule of thumb of sample collection in comprehensive on-line 2D-LC (4 samples/peak) been followed.     

Selectivity of Transport of Sodium, Magnesium, and Calcium Ions through a Sulfo-Cationite Membrane in Mixtures of Solutions of Their Chlorides

The transport numbers and the selectivity of transport of sodium, magnesium, and calcium ions through a heterogeneous sulfo-cationite membrane in solutions of sodium, magnesium, and calcium chlorides and their mixtures are studied at various current densities. Equations for calculating the selectivity of transport of the ions through the membrane are suggested for two extreme cases. One case corresponds to low currents, when one can assume that the membrane is at equilibrium with the outside solution. The selectivity of transport of the ions is defined in this case by their migration through the membrane. The other case occurs at currents that are close to a limiting value. Under these conditions the transport of the ions through the membrane is defined by their transport through a diffusion layer that forms near the membrane surface. Calculations with the aid of these equations satisfactorily conform to experiment. The deviation from calculation in the case of the magnesium cation is connected probably with its hydration being substantially greater as compared with sodium and calcium. It is established that the selectivity of transport of the ions through the membrane may be controlled to a certain extent by varying the current density.__________Translated from Elektrokhimiya, Vol. 41, No. 8, 2005, pp. 997–1000.Original Russian Text Copyright © 2005 by Greben’, Rodzik.     

Hydroarylation of Styrenes with Electron-Rich Arenes Over Acidic Ion-Exchange Resins

A series of acidic cation-exchange resins were used for the hydroarylation of resorcinol with styrene, in which resin D072 exhibited the excellent catalytic performance in this reaction with 99% conversion of styrene and 90% selectivity of 4-(1-phenylethyl)resorcinol. It was applied to the hydroarylation of various electron-rich arenes with styrenes, and the hydroarylated products were quantitatively obtained. This catalyst could be used for four consecutive runs with slight decrease in activity. The hydroarylation of resorcinol with styrene over resin D072 in a fixed bed was completed effectively with 94% selectivity and 99% conversion, and this green continuous process is potentially applicable to large-scale productions.     

Investigation of the mass transfer processes during the desalination of water containing phenol and sodium chloride by electrodialysis

Oxidation processes are used in wastewater treatment when conventional processes are not effective due to the presence of recalcitrant organic contaminants, like phenol. However, the presence of ionic compounds associated with organic pollutants may retard the oxidation. In this work the transport of species contained in an aqueous solution of phenol containing sodium chloride was evaluated in an electrodialysis (ED) system. An experimental study was carried out in which the influence of the process variables on the phenol loss and sodium chloride removal was investigated. Experiments were also performed without current, in order to determine the phenol transfer due to diffusion. The phenol and salt concentration variations in the ED compartments were measured over time, using dedicated procedures and an experimental design to determine the global characteristic parameters. A phenomenological approach was used to relate the phenol, salt and water fluxes with the driving forces (concentration and electric potential gradients). Under ED conditions, two contributions were pointed out for the phenol transport, i.e. diffusion and convection, this latter coming from the water flux due to electroosmosis related to the migration of salts. The fitting of the parameters of the transport equations resulted in good agreement with the experimental results over the range of conditions investigated.     

Chromatographic evaluation of reversed-phase/anion-exchange/cation-exchange trimodal stationary phases prepared by electrostatically driven self-assembly process

This work describes chromatographic properties of reversed-phase/cation-exchange/anion-exchange trimodal stationary phases. These stationary phases were based on high-purity porous spherical silica particles coated with nano-polymer beads using an electrostatically driven self-assembly process. The inner-pore area of the material was modified covalently with an organic layer that provided both reversed-phase and anion-exchange properties while the outer surface was coated with nano-sized polymer beads with strong cation-exchange characteristics. This design ensured spatial separation of the anion-exchange and the cation-exchange regions, and allowed reversed-phase, anion-exchange and cation-exchange retention mechanisms to function simultaneously. Chromatographic evaluation of ions and small molecules suggested that retention of ionic analytes was influenced by the ionic strength, pH, and mobile phase organic solvent content, and governed by both ion-exchange and hydrophobic interactions. Meanwhile, neutral analytes were retained by hydrophobic interaction and was mainly affected by mobile phase organic solvent content. Depending on the specific application, selectivity could be optimized by adjusting the anion-exchange/cation-exchange capacity ratio (selectivity), which was achieved experimentally by using porous silica particles with different surface areas.     

Distribution and Assessment of Heavy Metals in Trifolium dubium (Little Hop Clover) and the Impact of Soil Quality

Trifolium dubium is an edible plant that is utilized in traditional medicine for its anti-inflammatory and wound-healing properties. In this study, T. dubium was assessed to determine the elemental uptake by the plant as a function of soil characteristics. Across 10 geographic locations in KwaZulu-Natal, South Africa, the concentration of elements in T. dubium were found to be (descending order) Ca?>?Mg?>?Fe?>?Zn?>?Mn?>?Se?>?Ni?>?Cr?>?Cu?>?Co?>?Pb?>?Cd?>?As. The site had an influence on elemental uptake by the plant; however, accumulation or exclusion of elements from soil was controlled to meet physiological requirements. Soil chemical characteristics showed T. dubium grew in slightly acidic soils (pH – 6.15 to 6.68). The findings of this study show T. dubium to contain adequate concentrations of essential elements with undetectable levels of toxic metals, making the herb safe for human consumption and for use in traditional medicine. The plant can also contribute to poor communities by ameliorating food insecurity.     

丙烯酸一缩二乙二醇酯合成动力学

对７３２＊型强酸性阳离子交换树脂催化酯化合成丙烯酸一缩二乙二醇酯动力学 进行了研究，测定并推算出反应级数、反应速度常数及活化能等动力学参数。在此基 上，得到了８５～９５℃范围内的反应通式，提出了该合成过程的反应机理。