2018
DOI: 10.2175/106143017x15131012188187
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Reduction of Imidacloprid by Sponge Iron and Identification of its Degradation Products

Abstract: In this study, imidacloprid was degraded by sponge iron in aqueous solution via chemical reduction. The effects of initial pH, reaction time, and operating model were investigated. Lower of pH was advantageous to the reduction degradation reaction. The influence of agitation was investigated in terms of reaction kinetics and degradation yield. Imidacloprid degradation with agitation showed first-order reaction kinetics with a reaction rate of 0.0235 min À1 , and degradation without agitation possessed two dist… Show more

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Cited by 14 publications
(5 citation statements)
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“…Based on the related products, it can be inferred that imidacloprid is degraded to produce 2-chloro-5-carboxy pyridine by hydroxylation and carbonylation, respectively. At the end of the three pathways, the pyridine ring undergoes dechlorination, and the final mineralization of imidacloprid is achieved [96][97][98][99][100][101].…”
Section: Degradation Of Imidacloprid By Physicochemical Methodsmentioning
confidence: 99%
“…Based on the related products, it can be inferred that imidacloprid is degraded to produce 2-chloro-5-carboxy pyridine by hydroxylation and carbonylation, respectively. At the end of the three pathways, the pyridine ring undergoes dechlorination, and the final mineralization of imidacloprid is achieved [96][97][98][99][100][101].…”
Section: Degradation Of Imidacloprid By Physicochemical Methodsmentioning
confidence: 99%
“…The final transformed products were monitored and analyzed using HPLC-ESI/MS and a reaction mechanism was proposed considering the different products (as shown in Scheme 7). [70] Yari et al, in 2019 developed a chemical free method for the degradation of imidacloprid pesticide in aqueous phase. The degradation analysis was carried out in ultraviolet C (UV-C) using ZnO and TiO 2 .…”
Section: Chemical Approachmentioning
confidence: 99%
“…The final transformed products were monitored and analyzed using HPLC‐ESI/MS and a reaction mechanism was proposed considering the different products (as shown in Scheme 7). [70] …”
Section: Approaches For the Elimination/degradation Of Imidaclopridmentioning
confidence: 99%
“…32 IMD urea was the principal degradation product by hydrolysis and in weak alkaline media, which has been proven to have lower toxicity than the parent compound and can be easily mineralized. 33,34 IMD guanidine was formed by the loss of the -NO 2 group aer H + attacking the moiety of N-NO 2 of IMD, 35 which showed higher mammalian toxicity than the parent compound. However, this intermediate could eventually be converted into nontoxic molecular fragments in the natural environment.…”
Section: Electroreduction Of Imidaclopridmentioning
confidence: 99%
“…While diverse microorganisms may potentially degrade insecticides, IMD is none biodegradable due to its high toxicity. 3,4 A lot of work has focussed on exploring effective methods for IMD treatment. Ultraviolet (UV) photolysis with photocatalysis and photo-Fenton's reagent are the most intensively applied technologies.…”
Section: Introductionmentioning
confidence: 99%