2013
DOI: 10.1016/j.chemosphere.2013.06.051
|View full text |Cite
|
Sign up to set email alerts
|

Advanced oxidation for the treatment of chlorpyrifos in aqueous solution

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

3
35
0

Year Published

2014
2014
2023
2023

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 85 publications
(38 citation statements)
references
References 36 publications
3
35
0
Order By: Relevance
“…The required dose for removal of 50% and 90% of PMD was summarized in Table 1. The results showed an electron beam radiolysis is an efficient method to degrade the refractory contaminants, agreeing with the previously reported studies [28,32,33].…”
Section: Determination Of Dose Constant and Kinetic Studysupporting
confidence: 92%
See 2 more Smart Citations
“…The required dose for removal of 50% and 90% of PMD was summarized in Table 1. The results showed an electron beam radiolysis is an efficient method to degrade the refractory contaminants, agreeing with the previously reported studies [28,32,33].…”
Section: Determination Of Dose Constant and Kinetic Studysupporting
confidence: 92%
“…Therefore, the Å OH plays a vital role in the PMD degradation. The positive effects of N 2 O and O 2 on the radiolysis of the target pollutants were also reported in other studies on the radiolytic degradation of organic compounds such as chlorpyrifos [28], 4-chloraniline [37], benzene sulfonate [38], 2,4-dichlorophenoxyacetic acid [39] and 2,4, 6-trinitrotoluene [32,40]:…”
Section: Effect Of Solution Ph On Pmd Degradationsupporting
confidence: 72%
See 1 more Smart Citation
“…G value is defined as the number of molecules formed or destroyed by absorbing 100 eV of energy [13]. The degradation efficiency of pollutant removal can be described by G-value during ionizing radiation calculated by equation (5) [14].…”
Section: Calculation Of G-valuementioning
confidence: 99%
“…In a word, chlorpyrifos oxon and TCP are two primary transformation products of chlorpyrifos, which are derived from the oxidation of the P S double bond into the P O bond and hydrolysis at the P O bond adjacent to the benzene ring, respectively. Although many researches have been conducted on the degradation of chlorpyrifos by photolysis [3,20], hydrolysis [10], and microorganisms [21], most of them have focused on the transformations of chlorpyrifos in soil and water. Chlorpyrifos can exist in both gas and particle phases in the ambient atmosphere because of its semivolatile nature (1.8 × 10 −5 mm Hg at 25 • C) [22][23][24][25].…”
Section: Chlorpyrifosmentioning
confidence: 99%