摘要
中性 pH 条件下,在β-环糊精(β-CD)水溶液中 N-溴代萘亚氨基乙二酸(BNIA)的紫外吸收光谱表现出萘基典型的吸收带,即位于232 nm 的~1B_b 带和位于286 nm 的~1L_a带。pb^(2+)离子与 BNIA 配位后,引起~1B_b带显著的减色效应,并使~1L_a 带红移,在268nm 和302 nm 处出现两个等吸收点。而其它金属离子没有影响。据此建立了选择性的 pb^(2+)离子传感器,线性范围为1.0×10^(-6)~1.0×10^(-5)mol/L(r^2=0.9937),检出限为1.0×10^(-6)~1.0×10^(-5)mol/L。
At neutral pH, absorption bands of bromonaphthyl iminodiacetic acid (BNIA) were observed at 232 nm (^1Bb band) and 286 nm (^1L, band) in β- cyclodextrin aqueous solution, displaying the typical absorption spectrum of naphthalene. The complexation of BNIA with Pb^2+ resulted in notable hypoehromic effect of ^1Bb band and bathochromic shift of ^1La band accompanying the isobestie points at 268 nm and 302 nm. Other metals had no significant influence. Based on the hypoehromic effect, the selective Pb^2+ sensor is constructed and linear range is 1.0×10^-6 - 1.0×10^-5 mol/L( P =0. 993 7) ,the limit of detection of Pb^2+ is 1.0×10^-6 mol/L.
出处
《化学传感器》
CAS
2005年第4期29-32,共4页
Chemical Sensors