校准曲线
六氟磷酸盐
溶剂
剥离(纤维)
检出限
离子液体
分析化学(期刊)
铜
离子
吡啶
吡啶
萃取(化学)
化学
材料科学
无机化学
色谱法
有机化学
催化作用
复合材料
药物化学
生物化学
作者
Zhong Wei Pan,Helen J. Zeng,Hualing Yang,Mei Yu,Z. Y. Wang,Wen‐Jeng Wu,X. Q. Huang
标识
DOI:10.1179/1432891714z.0000000001093
摘要
Copper (Cu2+) ion was determined at micro level by diethyldithiocarbamate (DDTC) spectrophotometry after temperature-dependent solid–liquid separation using N-butyl pyridinium hexafluorophosphate ([BPy]PF6) as a solid solvent and DDTC as an extractant. The results showed that ions can be extracted 100% by DDTC–[BPy]PF6 at pH = 10·20. The extracted species was neutral Cu(DDTC)mCl2 (m = 1) based on slope analysis in the Cu2+–[BPy]PF6–DDTC temperature-dependent solid–liquid separation system. The recovery of Cu2+ extracted into DDTC–[BPy]PF6 can be achieved using 2 mol L−1 HNO3 as stripping agents. Back extraction method was adopted for the detection and quantification of Cu2+ ions using the DDTC spectrometry. The calibration curve was Y = 0·00328 + 0·10279X (correlation coefficient = 0·99922), the linear calibration range was 7·68 × 10−2 0·768 μg mL−1 and the limit of detection was 1·28 × 10−2 μg mL−1 for Cu2+. In this method, the contents of Cu2+ in Tieguanyin tea were determined with relative standard deviations (n = 5) of 2·82% and recoveries in the range of 96·6–108·5%.
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