西华师范大学学报:自然科学版
西華師範大學學報:自然科學版
서화사범대학학보:자연과학판
Journal of China West Normal University:Natural Science Edition
2012年
4期
386-391
,共6页
甲苯胺蓝%多壁碳纳米管%修饰电极%盐酸吡哆辛
甲苯胺藍%多壁碳納米管%脩飾電極%鹽痠吡哆辛
갑분알람%다벽탄납미관%수식전겁%염산필치신
toluidine blue%multi-walled carbon nanotubes%modified electrode%vitamin B6
制备了聚甲苯胺蓝、碳纳米管及二者复合修饰的4种修饰电极,以循环伏安法研究盐酸吡哆辛在几种修饰电极上的结果表明:聚甲苯胺蓝/多壁碳纳米管修饰电极对盐酸吡哆辛的电化学响应最佳,峰电位负移45mV,峰电流约为裸玻碳电极的3倍.盐酸吡哆辛在聚甲苯胺蓝/多壁碳纳米管修饰电极上是扩散控制不可逆氧化过程,电子转移数为1,质子数为1,电极活化面积为0.0409cm^2,扩散系数为6.3433×10^-4cm^2/s.氧化峰电流与浓度在8.0×10^-6-4.0×10^-4mol/L范围内呈良好的线性关系,线性方程为:ip(A)=-1.9865×10^-6-0.1052c(mol/L),R=-0.9968,检出限为2.0×10^-6mol/L,样品回收率为:92.63%-101.50%.
製備瞭聚甲苯胺藍、碳納米管及二者複閤脩飾的4種脩飾電極,以循環伏安法研究鹽痠吡哆辛在幾種脩飾電極上的結果錶明:聚甲苯胺藍/多壁碳納米管脩飾電極對鹽痠吡哆辛的電化學響應最佳,峰電位負移45mV,峰電流約為裸玻碳電極的3倍.鹽痠吡哆辛在聚甲苯胺藍/多壁碳納米管脩飾電極上是擴散控製不可逆氧化過程,電子轉移數為1,質子數為1,電極活化麵積為0.0409cm^2,擴散繫數為6.3433×10^-4cm^2/s.氧化峰電流與濃度在8.0×10^-6-4.0×10^-4mol/L範圍內呈良好的線性關繫,線性方程為:ip(A)=-1.9865×10^-6-0.1052c(mol/L),R=-0.9968,檢齣限為2.0×10^-6mol/L,樣品迴收率為:92.63%-101.50%.
제비료취갑분알람、탄납미관급이자복합수식적4충수식전겁,이순배복안법연구염산필치신재궤충수식전겁상적결과표명:취갑분알람/다벽탄납미관수식전겁대염산필치신적전화학향응최가,봉전위부이45mV,봉전류약위라파탄전겁적3배.염산필치신재취갑분알람/다벽탄납미관수식전겁상시확산공제불가역양화과정,전자전이수위1,질자수위1,전겁활화면적위0.0409cm^2,확산계수위6.3433×10^-4cm^2/s.양화봉전류여농도재8.0×10^-6-4.0×10^-4mol/L범위내정량호적선성관계,선성방정위:ip(A)=-1.9865×10^-6-0.1052c(mol/L),R=-0.9968,검출한위2.0×10^-6mol/L,양품회수솔위:92.63%-101.50%.
Polymeric toluidine blue and carbon nanotubes and four kinds of modified electrodes were prepared. The electrochemical behavior of VB6 at modified electrodes were studied with cyclic vohammetry. The results indicated that the polymeric' toluidine blue/multi-walled carbon nanotubes modified electrode showed excellent electrochemical activities towards VB6,peak potential shifted negatively 45 mV,the peak current is 2 times higher than the bare glass electrode, the oxidation of VB6 on PTB/MWNT/GC was irreversible and mainly controlled by diffusion. The electron transfer number was 1, proton transfer number was 1, the effective area of electrode was 0. 0409 cm^2, diffusion eoeffcient was 6. 3433 × 10^-4 cm^2/s. A good linearity relationship between peak current and concentration in the range of 8.0 × 10^-6 - 4. 0 × 10^-4mol/L was found, of which the equation was ip (A) = - 1. 9865 × 10^-6 - 0. 1052c(mol/L) , the correlative coefficient R = -0. 9968, and detection limit was 2.0 × 10^-6mol/L. The sample recovery was between 92.63% and 101.50%