Xu Tingting, Gao Huanli, Rojas Orlando J, Dai Hongqi
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, International Innovation Center for Forest Chemicals and Materials, College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing 210037, China.
Bioproducts Institute, Departments of Chemical and Biological Engineering, Chemistry and Wood Science, The University of British Columbia, 2360 East Mall, Vancouver, BC V6T 1Z3, Canada.
Polymers (Basel). 2023 May 23;15(11):2424. doi: 10.3390/polym15112424.
In this work, a conductive hydrogel was successfully synthesized, taking advantage of the high number density of active amino and hydroxyl groups in carboxymethyl chitosan and sodium carboxymethyl cellulose. These biopolymers were effectively coupled via hydrogen bonding with the nitrogen atoms of the heterocyclic rings of conductive polypyrrole. The inclusion of another biobased polymer, sodium lignosulfonate (LS), was effective to achieve highly efficient adsorption and in-situ reduction of silver ions, leading to silver nanoparticles that were embedded in the hydrogel network and used to further improve the electro-catalytic efficiency of the system. Doping of the system in the pre-gelled state led to hydrogels that could be easily attached to the electrodes. The as-prepared silver nanoparticle-embedded conductive hydrogel electrode exhibited excellent electro-catalytic activity towards hydroquinone (HQ) present in a buffer solution. At the optimum conditions, the oxidation current density peak of HQ was linear over the 0.1-100 μM concentration range, with a detection limit as low as 0.12 μM (signal-to-noise of 3). The relative standard deviation of the anodic peak current intensity was 1.37% for eight different electrodes. After one week of storage in a 0.1 M Tris-HCl buffer solution at 4 °C, the anodic peak current intensity was 93.4% of the initial current intensity. In addition, this sensor showed no interference activity, while the addition of 30 μM CC, RS, or 1 mM of different inorganic ions does not have a significant impact on the test results, enabling HQ quantification in actual water samples.
在这项工作中,利用羧甲基壳聚糖和羧甲基纤维素钠中活性氨基和羟基的高数量密度,成功合成了一种导电水凝胶。这些生物聚合物通过氢键与导电聚吡咯杂环的氮原子有效偶联。加入另一种生物基聚合物木质素磺酸钠(LS)可有效实现银离子的高效吸附和原位还原,从而形成嵌入水凝胶网络的银纳米颗粒,用于进一步提高该系统的电催化效率。在预凝胶状态下对该系统进行掺杂,得到的水凝胶能够轻松附着在电极上。所制备的嵌入银纳米颗粒的导电水凝胶电极对缓冲溶液中的对苯二酚(HQ)表现出优异的电催化活性。在最佳条件下,HQ的氧化电流密度峰在0.1 - 100 μM浓度范围内呈线性,检测限低至0.12 μM(信噪比为3)。八个不同电极的阳极峰电流强度的相对标准偏差为1.37%。在4℃的0.1 M Tris - HCl缓冲溶液中储存一周后,阳极峰电流强度为初始电流强度的93.4%。此外,该传感器无干扰活性,加入30 μM的CC、RS或1 mM不同无机离子对测试结果无显著影响,能够对实际水样中的HQ进行定量分析。