首页> 外文期刊>Desalination and water treatment >Solid-phase extraction of trace Ni(Ⅱ) ions on ethylenediamine-silica material synthesized by sol-gel method
【24h】

Solid-phase extraction of trace Ni(Ⅱ) ions on ethylenediamine-silica material synthesized by sol-gel method

机译:溶胶-凝胶法在乙二胺-二氧化硅材料上固相萃取痕量Ni(Ⅱ)离子

获取原文
获取原文并翻译 | 示例
           

摘要

A solid-phase extraction method using ethylenediamine-silica (EDA-SIL) material for the determination of Ni(Ⅱ) ions at trace level by flame atomic absorption spectrometry (FAAS) was presented in this study. EDA-SIL was synthesized with 3-(2-aminoethylamino) propyltri-methoxysilane (EDA-silane) and tetraethyl orthosilicate by sol-gel technique performing acidic hydrolysis and basic gelation procedure. EDA-SIL was characterized by FT-IR and C, H, and N elemental analysis. Solid-phase extraction of Ni(Ⅱ) ions was carried out using mini column filled with EDA-SIL. The important variables governing the recovery of Ni(Ⅱ) including pH, flow rate, eluent type, eluent volume, and matrix ions were studied. At the optimum preconcentration conditions, the recovery of Ni(Ⅱ) was found to be 100 ±3% at 95% confidence level. The detection limit of Ni(Ⅱ) was calculated based on the three times of standard deviation of blanks and found to be 0.32 ng mL~(-1) using a preconcentration factor of 50. The developed method was validated using certified water samples (Ontario Lake water, NWTMDA-54.4) and applied to synthetic sea water samples for the determination of Ni concentration by FAAS.
机译:提出了一种用乙二胺-二氧化硅(EDA-SIL)材料固相萃取的火焰原子吸收光谱法(FAAS)测定痕量镍(Ⅱ)离子的方法。用3-(2-氨基乙基氨基)丙基三甲氧基硅烷(EDA-硅烷)和原硅酸四乙酯通过溶胶-凝胶技术进行酸性水解和碱性胶凝步骤合成了EDA-SIL。通过FT-IR和C,H和N元素分析对EDA-SIL进行了表征。 Ni(Ⅱ)离子的固相萃取采用填充有EDA-SIL的微型柱进行。研究了影响Ni(Ⅱ)回收率的重要变量,包括pH,流速,洗脱液类型,洗脱液体积和基质离子。在最佳预富集条件下,置信水平为95%时,Ni(Ⅱ)的回收率为100±3%。根据空白标准偏差的三倍计算得出Ni(Ⅱ)的检出限,使用50的预浓缩系数发现其为0.32 ng mL〜(-1)。该方法已通过认证水样的验证(安大略省湖水(NWTMDA-54.4),并用于合成海水样品,通过FAAS测定镍浓度。

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