首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Silica gel modified with 1-(2-aminoethyl)-3-phenylurea for selective solid-phase extraction and preconcentration of Sc(III) from environmental samples
【24h】

Silica gel modified with 1-(2-aminoethyl)-3-phenylurea for selective solid-phase extraction and preconcentration of Sc(III) from environmental samples

机译:用1-(2-氨基乙基)-3-苯基脲改性的硅胶用于选择性固相萃取和预浓缩环境样品中的Sc(III)

获取原文
获取原文并翻译 | 示例
           

摘要

A new method that utilizes 1-(2-aminoethyl)-3-phenylurea-modified silica gel as a solid-phase extractant has been developed for preconcentration of trace Sc(III) prior to the measurement by inductively coupled plasma atomic emission spectrometry (ICP-AES). Experimental conditions for effective adsorption of trace level of Sc(III) were optimized using batch and column procedures in detail. The optimum pH value for the separation of Sc(III) on the new sorbent was 4 and complete elution of Sc(III) from the sorbent surface was carried out using 1.0 mL of 0.1 mol L-1 HCL Common coexisting ions did not interfere with the separation and determination of the analyte. The maximum static adsorption capacity of the sorbent at optimum conditions was found to be 32.5 mg g(-1) while the time of 95% adsorption was less than 2 min. The detection limit of present method was found to be 0.091 mu g g(-1), and the relative standard deviation (RSD) was lower than 3.0% (n = 8). The method was successfully applied for the preconcentration of trace Sc(III) in the environmental samples with satisfactory results.
机译:已开发出一种新的方法,该方法利用1-(2-氨基乙基)-3-苯基脲改性的硅胶作为固相萃取剂,用于在电感耦合等离子体原子发射光谱法(ICP)测量之前对痕量Sc(III)进行预浓缩。 -AES)。有效的吸附痕量Sc(III)的实验条件已使用批处理和色谱柱程序进行了详细优化。在新吸附剂上分离Sc(III)的最佳pH值为4,使用1.0 mL的0.1 mol L-1 HCL从吸附剂表面完全洗脱Sc(III)常见的共存离子不会干扰分析物的分离和测定。发现在最佳条件下吸附剂的最大静态吸附容量为32.5 mg g(-1),而95%吸附的时间少于2分钟。本方法的检出限为0.091μg g(-1),相对标准偏差(RSD)低于3.0%(n = 8)。该方法成功用于环境样品中痕量Sc(III)的富集,结果令人满意。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号