Li Xin-Ai, Zhou Dong-Mei, Xu Jing-Juan, Chen Hong-Yuan
State Key laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008, China; Key Lab of Analytical Chemistry for Life Science (MOE), School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Talanta. 2007 Feb 28;71(3):1130-5. doi: 10.1016/j.talanta.2006.06.009. Epub 2006 Jul 7.
In-channel indirect amperometric detection mode for microchip capillary electrophoresis with positive separation electric field is successfully applied to some heavy metal ions. The influences of separation voltage, detection potential, the concentration and pH value of running buffer on the response of the detector have been investigated. An optimized condition of 1200V separation voltage, -0.1V detection potential, 20mM (pH 4.46) running buffer of 2-(N-morpholino)ethanesulfonic acid (MES)+l-histidine (l-His) was selected. The results clearly showed that Pb(2+), Cd(2+), and Cu(2+) were efficiently separated within 80s in a 3.7cm long native separation PDMS/PDMS channel and successfully detected at a single carbon fibre electrode. The theoretical plate numbers of Pb(2+), Cd(2+), and Cu(2+) were 1.2x10(5), 2.5x10(5), and 1.9x10(5)m(-1), respectively. The detection limits for Pb(2+), Cd(2+), and Cu(2+) were 1.3, 3.3 and 7.4muM (S/N=3).
正分离电场下用于微芯片毛细管电泳的通道内间接安培检测模式成功应用于某些重金属离子。研究了分离电压、检测电位、运行缓冲液的浓度和pH值对检测器响应的影响。选择了1200V分离电压、-0.1V检测电位、20mM(pH 4.46)的2-(N-吗啉代)乙磺酸(MES)+L-组氨酸(L-His)运行缓冲液的优化条件。结果清楚地表明,Pb(2+)、Cd(2+)和Cu(2+)在3.7cm长的原生分离PDMS/PDMS通道内80s内有效分离,并在单碳纤维电极上成功检测。Pb(2+)、Cd(2+)和Cu(2+)的理论塔板数分别为1.2×10(5)、2.5×10(5)和1.9×10(5)m(-1)。Pb(2+)、Cd(2+)和Cu(2+)的检测限分别为1.3、3.3和7.4μM(S/N=3)。