摘要
本实验用磺化四苯基卟啉作柱前衍生试剂,研究了在Hg(Ⅱ)催化下,于pH5.5时,TPPS_4与Mn(Ⅱ)、Zn(Ⅱ)、Cu(Ⅱ)的配位反应,提出了以苄基三乙基氯化铵作离子对试剂,反相离子对高效液相色谱-光度法分离和测定痕量Mn(Ⅱ)、Zn(Ⅱ)、Cu(Ⅱ)的新方法,检测下限(×10^(-9)g/mL):Mn^(2+)0.15,Zn^(2+)0.20,Cu^(2+)0.11。所确立的方法用于茶汤中锰、锌、铜的测定,结果满意。
MnTPPS_4,ZnTPPS_4 and CuTPPS_4 are formed by reaction of TPPS_4 and the metal ions at pH5.5 using Hg ̄(2+)as the catalyst.Then they are separated on a ODS column within 10 minutes using a eluent composed of acetonitrile-water(27.5%)solution containing 50 mmol/L benzyltriethylammonium chloride(ion-pair reagent)and 20 mmol/L acetic acid-sodium acetate(pH6.4)and detected at 415 nm. The detection limit(×10(-9)g/mL) for Mn, Zn and Cu are 0.15,0.20 and 0.11 respectively, Trace amount of Mn, Zn, and Cu in tea fushiom has been successfully determined by this method.
出处
《分析测试学报》
CAS
CSCD
1994年第5期64-67,共4页
Journal of Instrumental Analysis
基金
浙江省自然科学基金
关键词
茶
TPPS4
高效液相色谱
锰
锌
铜
Ion-pair high performance liquid chromatography
Meso-tetra(4-sulfophenyl)porphyrin,Benzyltriethylammonium chloride
Mn(Ⅱ)
Zn(Ⅱ)
Cu(Ⅱ).