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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Separation of superparamagnetic magnetite nanoparticles by capillary zone electrophoresis using non‐complexing and complexing electrolyte anions and tetramethylammonium as dispersing additive
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Separation of superparamagnetic magnetite nanoparticles by capillary zone electrophoresis using non‐complexing and complexing electrolyte anions and tetramethylammonium as dispersing additive

机译:使用非络合和络合电解质阴离子和四甲基铵用毛细管区电泳将超顺磁磁铁矿纳米粒子分离为分散添加剂

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Abstract Separations of bare superparamagnetic magnetite nanoparticles (BSPMNPs, approx. 11 nm diameter) was performed using non‐complexing (nitrate) and complexing (chloride, citrate and phosphate) electrolyte ions with additions of tetramethylammonium hydroxide (TMAOH), which is commonly applied to control the synthesis of stable iron oxides. The use of TMAOH as a background electrolyte (BGE) additive for capillary electrophoresis (CE) separations provided for the first time electropherograms of BSPMNPs exhibiting symmetrical and highly reproducible peaks, free of spurious spikes characteristic of nanoparticle clusters. Consequently, accurate determination of the electrophoretic effective mobility of BSPMNPs was possible, yielding a value of ?3.345E‐08 m 2 V ?1 s ?1 (relative standard deviation (RSD) of 0.500%). The obtained mobilities of BSPMNPs in the presence of various electrolyte ions show that the degree of complexation with the surface of BSPMNPs follows the order chloride citrate phosphate, correlating with the stabilities of Fe(III) complexes with the respective anions. Finally, bare and carboxylated iron oxide nanoparticles were successfully separated in only 10 min using 10 mM Tris‐nitrate containing 20?mM of TMAOH as electrolyte. Our findings show that simple and rapid CE experiments are an excellent tool to characterise and monitor properties and interactions of iron oxide nanoparticles with other molecules for surface modification purposes.
机译:裸超顺磁性纳米粒子(BSPMNPs,约11纳米的直径。)的摘要分离用非络合(硝酸盐)和络合(氯化物,柠檬酸盐和磷酸盐)电解质离子与氢氧化四甲铵(TMAOH)的添加,其通常适用于执行控制稳定的铁氧化物的合成。使用TMAOH的作为背景电解质(BGE)添加剂用于毛细管电泳(CE)提供了一种用于呈现对称和高度可重现的峰,游离纳米颗粒簇的特性杂散尖峰BSPMNPs的第一次电泳分离。因此,BSPMNPs的电泳有效迁移率的准确确定是可能的,得到的?3.345E-08米2 V·1秒的值α1(相对标准偏差(0.500%RSD))。将得到的各种电解质离子的存在BSPMNPs的迁移率表明,与BSPMNPs的表面络合的程度如下顺序氯化物<柠檬酸<磷酸酯,以Fe(III)络合物的与相应阴离子的稳定性相关。最后,裸露和羧化的氧化铁纳米颗粒在仅10分钟使用含有20的10mM Tris-硝酸盐成功分离?TMAOH的毫作为电解质。我们的研究结果表明,简单和快速的CE实验是表征和监测特性和与其它分子进行表面改性目的的氧化铁纳米颗粒的相互作用的优秀工具。

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