Determination of Palladium and Platinum by Solid Phase Extraction and High Performance Liquid Chromatography
Qun Hu
Key Laboratory of Ethnic Medicine Resource Chemistry (Yunnan University of Nationalities), State Ethnic Affairs Commission & MInistry of Education, Kunming 650031, P.R. China; Yunnan Academy of Tobacco Science, Kunming 650106, P.R. China
Yinke Li
Key Laboratory of Ethnic Medicine Resource Chemistry (Yunnan University of Nationalities), State Ethnic Affairs Commission & MInistry of Education, Kunming 650031, P.R. China; Faculty of Sciences, Yuxi Normal University, Yuxi 653100, P.R. China
Bo Yang
Faculty of Sciences, Yuxi Normal University, Yuxi 653100, P.R. China
Lin Hu
Key Laboratory of Ethnic Medicine Resource Chemistry (Yunnan University of Nationalities), State Ethnic Affairs Commission & MInistry of Education, Kunming 650031, P.R. China
Yanqing Ye
Key Laboratory of Ethnic Medicine Resource Chemistry (Yunnan University of Nationalities), State Ethnic Affairs Commission & MInistry of Education, Kunming 650031, P.R. China
Qiufen Hu
Key Laboratory of Ethnic Medicine Resource Chemistry (Yunnan University of Nationalities), State Ethnic Affairs Commission & MInistry of Education, Kunming 650031, P.R. China ; Faculty of Sciences, Yuxi Normal University, Yuxi 653100, P.R. China
Corresponding Author(s) : Qiufen Hu
huquiufena@163.com
Asian Journal of Chemistry,
Vol. 24 No. 10 (2012): Vol 24 Issue 10
A new method for the determination of palladium and platinum ions using high performance liquid chromatography equipped with on-line solid phase extraction was developed. The palladium and platinum ions were derivatized with 2-(2-quinolinylazo)-1,3-diaminobenzene (QADAB) to form coloured chelate. The Pd-QADAB and Pt-QADAB chelates were then enriched on an enrichment column using a 0.05 mol L-1 of phosphoric acid as mobile phase. After the enrichment was completed, the retained chelates were back-flushed to the analytical column. The separation of chelates on the analytical column [CQUITY UPLC BEH C18 (1.7 μm 4.6 × 50 mm)] was satisfactory when 40 % acetonitrile (containing 0.05 mol L-1 of phosphoric acid and 0.1 % of triton X-100) was used as mobile phase. The Pt-QADAB and Pd-QADAB chelates were separated completely within 2.5 min. The detection limits (S/N = 3) for palladium and platinum were 1.0 ng L-1 and 1.2 ng L-1, respectively. The method was applied to the determination of palladium and platinum in water samples with good results.
Hu, Q., Li, Y., Yang, B., Hu, L., Ye, Y., & Hu, Q. (2012). Determination of Palladium and Platinum by Solid Phase Extraction and High Performance Liquid Chromatography. Asian Journal of Chemistry, 24(10), 4250–4252. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/9629