Abstract:This work describes the chemical synthesis of antimony oxide nanoparticles (AONPs), polyaniline (PANI), acid functionalized single-walled carbon nanotubes (fSWCNTs), and the nanocomposite (AONP-PANI-SWCNT) as catalyst for the trace detection of lindane. Successful synthesis of the nanomaterials was confirmed by Fourier transform infrared (FT-IR) spectroscopy, ultraviolet-visible (UV-Vis) spectroscopy, x-ray diffraction (XRD) spectroscopy, and scanning electron microscopy (SEM). Cyclic voltammetry (CV) and elec… Show more
“…Information on the preparation and characterization of AONPs, PANI, fSWCNTs has been reported in our previous studies [ 39 ].…”
Section: Methodsmentioning
confidence: 99%
“…The resultant mixture was stirred at room temperature for 48 h to obtain a putty form of AONP-PANI-SWCNTs composite. This nanocomposite was dried overnight at 25 °C in order to evaporate the solvent [ 39 ]. The drop-cast method was used for the modification of the electrode.…”
This report narrates the successful application of a fabricated novel sensor for the trace detection of endosulfan (EDS). The sensor was made by modifying a glassy-carbon electrode (GCE) with polyaniline (PANI), chemically synthesized antimony oxide nanoparticles (AONPs), acid-functionalized, single-walled carbon nanotubes (fSWCNTs), and finally, the AONP-PANI-SWCNT nanocomposite. The electrochemical properties of the modified electrodes regarding endosulfan detection were investigated via cyclic voltammetry (CV) and square-wave voltammetry. The current response of the electrodes to EDS followed the trend GCE-AONP-PANI-SWCNT (−510 µA) > GCE-PANI (−59 µA) > GCE-AONPs (−11.4 µA) > GCE (−5.52 µA) > GCE-fSWCNTs (−0.168 µA). The obtained results indicated that the current response obtained at the AONP-PANI-SWCNT/GCE was higher with relatively low overpotential compared to those from the other electrodes investigated. This demonstrated the superiority of the AONP-PANI-SWCNT-modified GCE. The AONP-PANI-SWCNT/GCE demonstrated good electrocatalytic activities for the electrochemical reduction of EDS. The results obtained in this study are comparable with those in other reports. The sensitivity, limit of detection (LoD), and limit of quantification (LoQ) of AONP-PANI-SWCNT/GCE towards EDS was estimated to be 0.0623 µA/µM, 6.8 µM, and 20.6 µM, respectively. Selectivity, as well as the practical application of the fabricated sensor, were explored, and the results indicated that the EDS-reduction current was reduced by only 2.0% when interfering species were present, whilst average recoveries of EDS in real samples were above 97%.
“…Information on the preparation and characterization of AONPs, PANI, fSWCNTs has been reported in our previous studies [ 39 ].…”
Section: Methodsmentioning
confidence: 99%
“…The resultant mixture was stirred at room temperature for 48 h to obtain a putty form of AONP-PANI-SWCNTs composite. This nanocomposite was dried overnight at 25 °C in order to evaporate the solvent [ 39 ]. The drop-cast method was used for the modification of the electrode.…”
This report narrates the successful application of a fabricated novel sensor for the trace detection of endosulfan (EDS). The sensor was made by modifying a glassy-carbon electrode (GCE) with polyaniline (PANI), chemically synthesized antimony oxide nanoparticles (AONPs), acid-functionalized, single-walled carbon nanotubes (fSWCNTs), and finally, the AONP-PANI-SWCNT nanocomposite. The electrochemical properties of the modified electrodes regarding endosulfan detection were investigated via cyclic voltammetry (CV) and square-wave voltammetry. The current response of the electrodes to EDS followed the trend GCE-AONP-PANI-SWCNT (−510 µA) > GCE-PANI (−59 µA) > GCE-AONPs (−11.4 µA) > GCE (−5.52 µA) > GCE-fSWCNTs (−0.168 µA). The obtained results indicated that the current response obtained at the AONP-PANI-SWCNT/GCE was higher with relatively low overpotential compared to those from the other electrodes investigated. This demonstrated the superiority of the AONP-PANI-SWCNT-modified GCE. The AONP-PANI-SWCNT/GCE demonstrated good electrocatalytic activities for the electrochemical reduction of EDS. The results obtained in this study are comparable with those in other reports. The sensitivity, limit of detection (LoD), and limit of quantification (LoQ) of AONP-PANI-SWCNT/GCE towards EDS was estimated to be 0.0623 µA/µM, 6.8 µM, and 20.6 µM, respectively. Selectivity, as well as the practical application of the fabricated sensor, were explored, and the results indicated that the EDS-reduction current was reduced by only 2.0% when interfering species were present, whilst average recoveries of EDS in real samples were above 97%.
“…From this perspective, conducting polymers combined with low loading of metallic species are good candidates for high-performance electrocatalysts due to their interesting structural and physical properties (Ghosh et al, 2015(Ghosh et al, , 2016(Ghosh et al, , 2017Wang et al, 2016a;Ramohlola et al, 2018). Among those polymers, polyaniline (PANI) has received tremendous attention in recent years in (bio)electrochemistry to be directly used as an electrode or indirectly as a supporting material (Wu et al, 2011;Silva et al, 2013;Boeva and Sergeyev, 2014;Xu and Minteer, 2014;Wang et al, 2016a;Cao et al, 2017;Torres et al, 2017;Feng et al, 2018;Masibi et al, 2018;Ramohlola et al, 2018;Shendkar et al, 2018;Bai et al, 2019). Torres and co-workers have shown that upon the introduction of Ni in a PANI-based electrode, the exchange current density (j 0 ) increases from 0.35 to 3.47 µA cm −2 , which indicates that the ability of electron transfer (driving force in electrocatalysis) is about one magnitude higher (Torres et al, 2017).…”
“…40 The absorption peaks at 1612, 1611, 1425, and 1422 cm À1 correspond to the amine and imine groups in BC-PANI and BC-PANI-Cu. [41][42][43][44] The peaks at 1313 and 1290 cm À1 correspond to the protonated state of PANI, 45,46 while the peaks at 861 and 864 cm À1 can be attributed to the head-to-tail coupling of the aniline monomers. 47,48 Thus, the FT-IR analysis confirmed the presence of PANI in the BC-PANI-Cu membrane.…”
This study presents a cost-effective method of enhancing the electrical conductivity and washing durability of bacterial cellulose (BC)-polyaniline (PANI) membrane by the addition of metal salt. In this study, two types of metal salts were tested: copper (II) sulfate and iron (II) sulfate. The optimal condition to produce BC-PANI-metal salt membranes was 0.05% (w/v) of copper (II) sulfate (copper salt). X-ray diffraction analysis showed that the crystallinity of BC-PANI increased after adding copper salt. According to the increased degree of crystallinity, the polymer chain structure of BC-PANI-copper salt (BC-PANI-Cu) was more organized than that of BC-PANI, as confirmed by scanning electron microscopy. In addition, this ordered structure of BC-PANI-Cu indicated enhanced electrical conductivity. Moreover, the addition of copper salt improved the electrical conductivity of BC-PANI to a level about 3.8 times higher than that of BC-PANI produced without metal salt, and it retained about 40% of its original electrical conductivity after three washing cycles. From the results, the addition of copper salt improved both the electrical conductivity and washing durability of the BC-PANI membrane.
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