Enhanced tris-(2-chloroisopropyl) phosphate degradation through ultraviolet driven peroxymonosulfate process: Kinetics, mechanism, residual toxicity assessment of intermediates products by proteomics
Creators
- 1. Guangdong Provincial Key Laboratory of Petrochemical Pollution Processes and Control, School of Environmental Science and Engineering, Guangdong University of Petrochemical Technology, Maoming, Guangdong 525000 (China)
- 2. Guangzhou Key Laboratory of Vacuum Coating Technologies and New Energy Materials, Guangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy Materials, Department of Physics, Jinan University, Guangzhou, Guangdong 510632 (China)
- 3. Guangdong Provincial Research Center for Environment Pollution Control and Remediation Materials, College of Life Science and Technology, Jinan University, Guangzhou 510632 (China)
- 4. Key Laboratory of Ministry of Education on Pollution Control and Ecosystem Restoration in Industry Clusters, School of Environment and Energy, South China University of Technology, Guangzhou 510006, Guangdong (China)
Description
Highlights: • A well removal performance on TCPP was realized via SO4− based AOPs treatment. • Degradation products involved in hydroxylation and dechlorination were proposed. • Toxicity of TCPP was weakened via oxidation treatment by proteomics analysis. • Metabolism network of E. coli was interfered by degradation intermediates of TCPP. • An incomplete mineralization is feasible and safe for TCPP elimination. Tris-(2-chloroisopropyl) phosphate (TCPP), one of emerging organic pollutants has aroused a growing concern due to its potential biotoxicity and persistence. Oxidation degradation of using SO4*− based AOPs was explored. A pseudo-first order kinetics reaction with the degradation rate constant at 0.1789 min−1 fitted the transformation of TCPP. SO4*− was the predominant oxidation species confirmed by scavenging assay. Five steady intermediates including C6H13Cl2O4P (m/z 251.0002), C3H8ClO4P (m/z 174.9922), C9H17Cl2O5P (m/z 307.0266), C9H17Cl2O6P (m/z 323.0217), C6H12ClO6P (m/z 247.0134) were screened by high resolution mass spectroscopy analysis. The influences of vital parameters, i.e., natural anions, pH value, humic acid (HA) and peroxymonosulfate (PMS) dose were tested. HA and alkaline conditions can significantly decreased the photocatalytic rate to inhibit removal efficiency. EE/O evaluation had also proved that a neutral condition and HA pretreatment were conductive to elevating removal efficiency and reducing energy consumption. Based on proteomics and metabolic network analysis, TCPP was effectively detoxified as its further transformation proceeded, which was proved by nucleotide metabolisms, citric acid metabolism, oxidative phosphorylation and amino acid biosynthesis. To summarize, an appropriate degradation of TCPP likewise are effective for its detoxification, indicating the feasibility and security of TCPP elimination using UV/PMS treatment.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2021.147583Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2021.147583;
- PII
- S0048969721026541;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 786
- Journal Page Range
- vp.
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54059181
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S46: INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND TECHNOLOGY;
- Descriptors DEI
- AMINO ACIDS; ANIONS; BIOSYNTHESIS; CITRIC ACID; DECHLORINATION; HUMIC ACIDS; HYDROXYLATION; MASS SPECTROSCOPY; NETWORK ANALYSIS; OXIDATION; PH VALUE; PHOTOCATALYSIS; REACTION KINETICS; ULTRAVIOLET RADIATION
- Descriptors DEC
- CARBOXYLIC ACIDS; CATALYSIS; CHARGED PARTICLES; CHEMICAL REACTIONS; DEHALOGENATION; ELECTROMAGNETIC RADIATION; HYDROXY ACIDS; IONS; KINETICS; ORGANIC ACIDS; ORGANIC COMPOUNDS; RADIATIONS; SPECTROSCOPY; SYNTHESIS
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.