首页> 外文期刊>Journal of the Brazilian Chemical Society >Adsorptive stripping voltammetric determination of nitroimidazole derivative on multiwalled carbon nanotube modified electrodes: influence of size and functionalization of nanotubes
【24h】

Adsorptive stripping voltammetric determination of nitroimidazole derivative on multiwalled carbon nanotube modified electrodes: influence of size and functionalization of nanotubes

机译:吸附剥离伏安法测定多壁碳纳米管修饰电极上的硝基咪唑衍生物:纳米管尺寸和功能化的影响

获取原文
       

摘要

1-Methyl-4-nitro-2-brominemethylimidazole (4-NimMeBr), was electrochemically reduced on mercury, glassy carbon and multiwalled carbon nanotubes (MWCNT) modified electrodes. 4-NimMeBr was adsorbed on the MWCNT modified electrode thus permitting the implementation of an adsorptive stripping voltammetric (ASV) method. We have used 4-NimMeBr as a prototype electroactive nitro compound to study the effect of both the size of the nanotubes and its functionalization by oxidation. The oxidized MWCNT forms better dispersions than the non-oxidized, producing electrode surface with higher density of MWCNT as was determined by electrochemical mapping using scanning electrochemical microscopy (SECM). Under the optimized conditions, the peak current was proportional to the concentration of 4-NimMeBr in the range of 10-6 mol L-1 to 10-4 mol L-1 with detection and quantification limits of 4.41×10-6 mol L-1 and 6.21×10-6 mol L-1, respectively. The sensibility of bare electrode was 0.01 μA per mmol L-1, which was lower than the value of 5.34 and 6.97 μA per mmol L-1 obtained using short and large oxidized MWCNT, respectively.
机译:1-甲基-4-硝基-2-溴甲基咪唑(4-NimMeBr)在汞,玻璃碳和多壁碳纳米管(MWCNT)修饰的电极上进行了电化学还原。 4-NimMeBr吸附在MWCNT修饰电极上,因此可以实施吸附溶出伏安法(ASV)。我们已使用4-NimMeBr作为原型电活性硝基化合物来研究纳米管尺寸及其通过氧化功能化的影响。氧化的MWCNT比未氧化的MWCNT形成更好的分散体,从而产生具有更高密度的MWCNT的电极表面,如通过使用扫描电化学显微镜(SECM)的电化学图所确定的。在最佳条件下,峰值电流与4-NimMeBr的浓度成正比,范围为10-6 mol L-1至10-4 mol L-1,检测和定量限为4.41×10-6 mol L-分别为1和6.21×10-6mol L-1。裸电极的灵敏度为0.01μA/ mmol L-1,这分别低于使用短和大型氧化MWCNT获得的5.34和6.97μA/ mmol L-1的值。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号