以交联聚乙烯醇为载体的离子交换剂对蛋白质的分离性能

本文对阴离子交换剂ＤＥＡ—ＰＶＴ常压液相离子交换色谱分离蛋白质的性能、分离条件进行了探讨。结果表明其对蛋白质的分离性能良好，容易洗脱。与载体交联聚乙烯醇相比，ＤＥＡ—ＰＶＴ对蛋白质的非特异性吸附明显降低。     

X-Ray Powder Diffraction Studies of Polyhydrates of Cross-Linked Tetraisoamylammonium Polyacrylates

X-ray powder diffraction studies were performed of the polyhydrates, formed at positive temperature in swelled grains of carboxylic cation-exchange resins in the form of tetraisoamylammonium (cross-linked tetraisoamylammonium polyacrylates, differing in the degree of cross-linking: 1, 2 and 3%). It was shown that the polyhydrates exist as the crystalline phase under specific conditions, determined earlier by DTA technique. Diffraction patterns of the samples, recorded at the temperature +3 ± 1 °C, indicate that the polyhydrates crystallize in hexagonal symmetry, the unit cell parameters are close to a=12.25 Å, c=12.72 Å and do not depend significantly upon the degree of cross-linking. The suppositions were made concerning the size of hydrate crystallites, formed in the swelled grains of the studied resins.This revised version was published online in July 2005 with a corrected issue number.     

Synthesis of enantiopure 1,2-diamine attached to cross-linked polystyrene and its application to an insoluble catalyst for asymmetric hydrogenation

A novel enantiopure 1,2-diamine (5) having two phenolic hydroxy groups was attached into chloromethylated polystyrene through benzyl ether linkage, which was used as a chiral ligand of the catalyst in asymmetric hydrogenation of acetophenone.     

Application of Ni(II)-imprinted cross-linked poly(methacrylic acid) synthesised through double-imprinting method for the on-line preconcentration of Ni(II) ions in aqueous media

The present paper describes the feasibility of on-line preconcentration of nickel ions from aqueous medium on Ni(II)-imprinted cross-linked poly(methacrylic acid) (IIP) synthesised through a double-imprinting method and their subsequent determination by FAAS. The proposed method consisted in loading the sample (20.0 mL, pH 7.25) through a mini-column packed with 50 mg of the IIP for 2 min. The elution step was performed with 1.0 mol L^?1 HNO₃ at a flow rate of 7.0 mL min^?1. The following parameters were obtained: quantification limit (QL) – 3.74 µg L^?1, preconcentration factor (PF) – 36, consumption index (CI) – 0.55 mL, concentration efficiency (CE) – 18 min^?1, and sample throughput – 25 h^?1. The precision of the procedure assessed in terms of repeatability for ten determinations was 5.6% and 2.5% for respective concentrations of 5.0 and 110.0 µg L^?1. Moreover, the analytical curve was obtained in the range of 5.0–180.0 µg L^?1 (r = 0.9973), and a 1.64-fold increase in the method sensitivity was observed when compared with the analytical curve constructed for the NIP (non-imprinted polymer), thus suggesting a synergistic effect of the Ni(II) ions and CTAB on the adsorption properties of the IIP. The practical application of the adsorbent was evaluated from an analysis of tap, mineral, lake and river water. Considering the results of addition and recovery experiments (90.2–100 %), the efficiency of this adsorbent can be ensured for the interference-free preconcentration of the Ni(II) ions.     

一种交联聚合物薄膜的表面引发聚合制备及其摩擦磨损性能

采用活性可控的表面引发原子转移自由基聚合方法,在硅片表面制备了聚3-(三甲氧基硅)丙基甲基丙烯酸酯聚合物刷,其中产物侧链的三甲氧基硅基团提供相邻分子间相互交联的位点而形成聚合物薄膜;采用衰减全反射红外光谱仪和原子力显微镜分析了薄膜的化学结构和微观形貌,利用椭圆偏光测厚仪和接触角测量仪测定了其厚度和水接触角,并利用微观和宏观摩擦磨损测试装置评价了薄膜的摩擦磨损性能.结果表明,所制备的薄膜具有聚合物的结构特征以及良好的减摩抗磨特性,且其抗磨能力随着厚度增加而增强.     

Biocatalytic process intensification via efficient biocatalyst immobilization,miniaturization, and process integration

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The structure of XLPE and the distribution of space charge

The formation and accumulation of space charge under charge treatment are investigated using PWP method. The interaction between space charge and the structure of XLPE is measured using infrared spectroscopy (IR) method. The related mechanism about space charge distribution and the structure of XLPE are discussed.     

Interaction of 1-anilinonaphthalene-8-sulphonate with cross-linked poly (N-vinyl-2-pyrrolidone)

The interaction of 1-anilinonaphthalene-8-sulphonate (ANS) with cross-linked poly(N-vinyl-2-pyrrolidone) (CPVP) was studied by the adsorption technique at different temperatures and at two different pH values. Analysis by the Scatchard method and the study made in the presence of urea showed that the iceberg structure of water affects the sorption of ANS to CPVP, leading to cooperativity. The observed Giles sorption isotherms at both the pH values were of theL-type which indicated the interaction of ANS in flat configuration with the binding site in CPVP. The sorption of ANS to CPVP was enhanced considerably at acidic pH due to some structural factors which also resulted in multilayer sorption at this pH. Comparison of binding of ANS to CPVP and to linear poly(N-vinyl-2-pyrrolidone) demonstrated the greater contribution of hydrophobic interaction in CPVP than in the linear polymer.     

Solid state 15N NMR study of 15N enriched melamine-formaldehyde resins

Molecular dynamics and structure of uncured and cured melamine-formaldehyde resins isotopically ¹⁵N enriched at amine sites were studied by solid-state ¹⁵N nuclear magnetic resonance (NMR). Spectra recorded with direct (DP) and cross-polarization (CP) pulse sequences reflect two motionally different regions arising from similar chemical structures. DP spectra of uncured resins at higher temperatures have narrow lines and the detection of slightly different structural units is possible. With increasing crosslinking resonances broaden and overlap and the direct detection of individual signals in cured resins is not possible. On the basis of variable contact time, variable spinning speed, and interrupted decoupling experiments three protonated and one nonprotonated group of signals are identified in the CP spectra for all samples. Short polarization-transfer rates, T_NH, for nonprotonated nitrogen in uncured and lightly cured samples reveal more effective hydrogen bonding in viscous and rubber-like resins compared to the highly cured rigid resins. The rigid portions of the resins exhibit longer T₁ and short T_1ρ relaxation times, while the shorter T₁ times and longer T_1ρ times are associated with the more mobile portion of samples. ©1995 John Wiley & Sons, Inc.     

偶氮苯聚合物全息光栅衍射效率和偏振特性研究

研究了不同偏振全息模式下基于交联偶氮苯聚合物薄膜的相位光栅的形成机理、衍射效率和偏振特性.利用琼斯矢量表征了正交线偏振(SP)和半行线偏振(SS)干涉模式下的偏振干涉场.基于SP和SS两种模式,制作了无明显表成起伏的纯折射率光栅和有表面起伏的浮雕光栅.偏光显微镜(POM)观测说明纯折射率光栅具有周期性的折射率分布;近场光学显微镜(SNOM)探测说明纯折射率光栅和浮雕光栅的表而起伏在5 nm以下和 85.23 nm.实验表明.当探测光为水平偏振时,纯折射率光栅的衍射效率达到22.2%.浮雕光栅只能达到1.65%.纯折射率光栅的0、 1级衍射光分别为水平和竖直线偏振光,偏振度达到0.9969和0.9963;浮雕光栅的0, 1级衍射光均为水平线偏振光.