4.7 Article

In-situ fabrication of polypyrrole composite with MoO3: An effective interfacial charge transfers and electrode materials for degradation and determination of acetaminophen

期刊

CHEMOSPHERE
卷 291, 期 -, 页码 -

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2021.132977

关键词

MoO3@PPy composite; Photodegradation; Electrochemical; Acetaminophen; Real samples

资金

  1. Ministry of Science and Technology (MOST), Taiwan [MOST 110-2113-M027-003-MY3]

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In this paper, MoO3@PPy composite was synthesized and utilized for photocatalytic degradation and electrochemical determination of acetaminophen (AP). The composite showed excellent catalytic activity and active surface area, and the effective charge transfer properties were confirmed by trapping experiments. The sensitivity and selectivity of the composite for AP determination were validated.
Pharmaceutical wastes, acetaminophen (AP) widely used in medical fields, is often discharged into water, causing harm to human health. Hence, there is an urgent need to effectively remove AP from wastewater systems. In this paper, polypyrrole (PPy) composite with MoO3 has been synthesized via an in-situ polymerization method. The as-prepared materials were thoroughly characterized by XRD, FT-IR, UV-DRS, SEM, TEM and mapping techniques. The as-prepared MoO3@PPy composite was utilized to removal of AP via photocatalytic degradation and electrochemical determination. Under optimized composite, MoO3@PPy (2) showed an excellent photocatalytic degradation and electrochemical determination of AP compared to pure MoO3 and all other composites. The higher catalytic activity was ascribed to the effective interfacial charges transfer, reduce the recombination and enhance the active surface area of electrode via a synergistic effect. The photocatalytic degradation mechanism, rate and kinetic of the reaction were investigated and discussed. The major active degradation species and an effective charge transfer properties were confirmed by trapping experiments and photocurrent spectra. In addition, the MoO3@PPy (2) modified GCE exhibit the AP determination activity by DPV with a linear range of 0.05-546 mu M. The limit of detection and sensitivity of electrode were 0.0007 mu M and 0.242 mu M-1 cm(-2) respectively. Moreover, the proposed electrode showed good selectivity, stability and reproducibility. This method was useful for the determination of AP in real samples.

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