The present study reports on the application of modified groundnut shell as a new, easily prepared, and stable sorbent for the extraction of trace amount of Cr(III) in aqueous solution. 2-Hydroxybenzaldiminoglycine was immobilized on groundnut shells in alkaline medium and then used as a solid phase for the column preconcentration of Cr(III). The elution was carried out with 3 mL of 2 mol L(-1) HCl. The amount of eluted Cr(III) was determined by spectrophotometry using cefaclor as a complexing reagent and by flame atomic absorption spectrometry (FAAS). Different experimental variables such as pH, amount of solid sorbent, volume and concentration of eluent, sample and eluent flow rate, and interference of other metal ions on the retention of Cr(III) were studied. Under the optimized conditions, the calibration curves were found to be linear over the concentration range of 13-104 and 10-75 μg L(-1) with a detection limit of 3.64 and 1.24 μg L(-1) for spectrophotometric method and FAAS, respectively. An enrichment factor of 200 and RSD of ±1.19-1.49 % for five successive determinations of 25 μg L(-1) were achieved. The column preconcentration was successfully applied to the analysis of tap water and underground water samples.

译文

:本研究报道了改性花生壳作为一种新型,易于制备且稳定的吸附剂在萃取水溶液中痕量Cr(III)中的应用。将2-羟基苯扎尔二氨基甘氨酸固定在碱性介质中的花生壳上,然后用作固相用于Cr(III)的柱预浓缩。用3 mL 2 mol L(-1)HCl进行洗脱。 Cr(III)的洗脱量通过使用头孢克洛作为络合剂的分光光度法和火焰原子吸收光谱法(FAAS)确定。研究了不同的实验变量,例如pH,固体吸附剂的量,洗脱液的体积和浓度,样品和洗脱液的流速以及其他金属离子对Cr(III)保留的干扰。在优化的条件下,发现校正曲线在13-104和10-75μgL(-1)的浓度范围内是线性的,分光光度法和FAAS的检出限为3.64和1.24μgL(-1)。 , 分别。连续5次测定25μgL(-1)的富集系数为200,相对标准偏差为±1.19-1.49%。柱预浓缩成功地用于自来水和地下水样品的分析。

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