摘要
研究了对磺酸基苯亚甲基若丹宁(SBDR)与Pd的显色反应及C18固相萃取小柱对显色络合物的固相萃取,并结合微波消化样品,提出了一种测定氰化渣中痕量Pd的方法,在pH=2.0的氯乙酸-氢氧化钠缓冲介质中,溴化十六烷基三甲胺(CTMAB)存在下,SBDR与Pd反应生成21稳定络合物,λmax=535nm,ε=7.79×104L·mol-1·cm-1。Pd含量在0.01~2.0μg/mL内符合比尔定律,方法用于氰化渣中痕量Pd的测定,结果令人满意。
Based on the color reaction of p-sulfobenzylidene-rhodanine (SBDR) with palladium (II) and the solid phase extraction of its colored complex with C18 cartridge, a new method for the determination of palladium in cyanide residue was studied. In pH 2.0 buffer solution medium and in the presence of CTMAB, SBDR can react with palladium to form a stable 2:1 complex. The molar absorptivity is 7.79×104 L·mol-1·cm-1 at 535 nm. Beer’s law is obeyed in the range of 0.01~2.0 μg/mL. The method was applied to the determination of palladium in cyanide residue with good results.
出处
《贵金属》
CAS
CSCD
2005年第1期39-42,共4页
Precious Metals
基金
云南省教育厅自然科学基金资助项目(No.0111143)
昆明贵金属研究所创新基金资助(No.2002-BY-01)。