Degradation of phenanthrene in sulfate radical based oxidative environment by nZVI-PDA functionalized rGO catalyst

• Published in: Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2018-12, Vol.354, p.541-552
• Main Authors: Gu, Mengbin, Sui, Qian, Farooq, Usman, Zhang, Xiang, Qiu, Zhaofu, Lyu, Shuguang
• Format: Article
• Language: English
• Subjects: Catalysis; Groundwater remediation; nZVI-PDA@rGO; Oxidation; Phenanthrene
• ISSN: 1385-8947; 1873-3212
• DOI: 10.1016/j.cej.2018.08.039

[Display omitted] •nZVI-PDA@rGO catalyst was applied into oxidative environments to remove PHE.•nZVI-PDA@rGO had a better catalytic reactivity than nZVI for PHE removal.•HO and SO4− were the predominant radicals in the nZVI-PDA@rGO/SPS, PMS system.•PHE degradation pathways were proposed in the two SO4− based oxidative systems. The ability of SO4− based advanced oxidation processes activated by nano zero-valent iron (nZVI) on reduced graphene oxide (rGO) functionalized by polydopamine (PDA) (nZVI-PDA@rGO) in degradation of phenanthrene (PHE) was investigated under various environmental conditions. The results showed that, compared with nZVI, the catalytic degradation of PHE was enhanced after anchoring nZVI on the PDA@rGO nanosheet in the activation of sodium persulfate (SPS) and peroxymonosulfate (PMS). The maximum PHE removal efficiency reached 95.9% and 98.7% in the nZVI-PDA@rGO/SPS (50 mg L−1/0.3 mM) and nZVI-PDA@rGO/PMS (50 mg L−1/0.0375 mM) systems, respectively. The effects of pH, anions and humic acid (HA) on the PHE degradation were tested in the nZVI-PDA@rGO coupling with PMS or SPS system. The higher PHE removal could be maintained in the nZVI-PDA@rGO/SPS system at pH up to 7.74 and in the nZVI-PDA@rGO/PMS system at pH up to 7.86, respectively. Cl− had a positive effect on PHE removal in both SPS and PMS systems, while a negative effect was observed in the presence of SO42−, NO3− and HCO3− (HCO3− > SO42− > NO3−). In addition, the PHE removal was inhibited significantly after addition of 50 mg L−1 HA. The radical scavenger tests were carried out to identify the dominant reactive oxygen species (ROSs), which demonstrated that SO4− and HO were the two primary ROSs responsible for the PHE removal. The intermediate products were identified by LC-MS and the degradation pathway of PHE was proposed.