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首页> 外文期刊>The Korean journal of chemical engineering >Highly improved adsorption selectivity of L-phenylalanine imprinted polymeric submicronanoscale beads prepared by modified suspension polymerization
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Highly improved adsorption selectivity of L-phenylalanine imprinted polymeric submicronanoscale beads prepared by modified suspension polymerization

机译:改性悬浮聚合制备的L-苯丙氨酸印迹聚合物亚微米/纳米级珠的吸附选择性大大提高

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Molecularly imprinted polymer (MIP) submicronanoscale beads selective for L-Phenylalanine (L-Phe) and D-Phe as well as non-imprinted beads were prepared by modified suspension polymerization involving agitation of the reaction mixture at high rotation speed under safe radical conditions. The effects of pH, template and concentration of racemate solution on the performance of the phenylalanine (Phe) imprinted polymeric submicronanoscale beads were studied. L-Phe-imprinted submicronanoscale beads prepared for the first time by modified suspension polymerization showed enhanced adsorption capacity and selectivity over those of D-Phe imprinted and non-imprinted beads. Maximum adsorption capacity, 0.35 mg/g, and selectivity, 1.62, of L-Phe imprinted submicronanoscale beads were higher than the adsorption capacities, 0.30 and 0.19 mg/g, and selectivities, 1.59 and 1.02, of D-Phe imprinted and non-imprinted submicronanoscale beads, respectively. FE-SEM analyses revealed that L- and D-Phe imprinted beads were larger (100 nm-1.5 ixri) than non-imprinted nanobeads (100-800 nm). 13~C CP-MAS NMR spectroscopy helped in correlating the bead sizes and the extent of reaction during polymerization. Similarly, FT-IR study was used for evaluation of structural characteristics of the prepared Phe-imprinted and non-imprinted beads. The preparation of Phe-imprinted submicronanoscale beads with improved adsorption and separation properties and the study of effect of template on the size and performance of the prepared beads are suitable from both economical and research point of view in MIP field.
机译:通过修饰的悬浮聚合反应制备了对L-苯丙氨酸(L-Phe)和D-Phe有选择性的分子印迹聚合物(MIP)亚微米/纳米珠,以及未印迹的珠粒,其中涉及在安全自由基下以高转速搅拌反应混合物的方法条件。研究了pH,模板和外消旋溶液的浓度对苯丙氨酸(Phe)印迹聚合物亚微米/纳米级微珠性能的影响。首次通过修饰的悬浮聚合制备的L-Phe印迹亚微米/纳米珠比D-Phe印迹和非印迹珠具有更高的吸附能力和选择性。 L-Phe印制的亚微米/纳米级珠的最大吸附容量0.35 mg / g和选择性1.62高于D-Phe印制和吸附的D-Phe的吸附容量0.30和0.19 mg / g以及选择性1.59和1.02非印迹亚微米/纳米级珠。 FE-SEM分析显示,L-和D-Phe印迹珠(100 nm-1.5 ixri)比非印迹纳米珠(100-800 nm)大。 13 C CP-MAS NMR光谱有助于关联珠的大小和聚合过程中的反应程度。同样,FT-IR研究用于评估制备的Phe印迹和非印迹珠的结构特征。从MIP领域的经济和研究角度来看,具有改进的吸附和分离特性的Phe印迹亚微米/纳米级微珠的制备以及模板对所制备微珠的尺寸和性能影响的研究都是合适的。

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