Degradation of microcystin-LR by highly efficient AgBr/Ag3PO4/TiO2 heterojunction photocatalyst under simulated solar light irradiation
Creators
- 1. School of Environment and Energy, Shenzhen Graduate School of Peking University, Shenzhen, 518055 (China)
- 2. Graduate School of Life and Environmental Science, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 (Japan)
- 3. School of Environmental Science and Engineering, Tianjin University, Tianjin, 300072 (China)
- 4. School of Water Resource and Environment, China University of Geosciences (Beijing), Beijing, 10083, P.R. China (China)
Description
Highlights: • AgBr/Ag3PO4/TiO2 consisting of less silver content possessed much higher photocatalytic activity than AgBr/Ag3PO4. • Reactive h+ and • OH played the major roles for MC-LR degradation by AgBr/Ag3PO4/TiO2. • AgBr/Ag3PO4/TiO2 photocatalyst was more stable than AgBr/Ag3PO4 in successive runs. • MC-LR was degraded into intermediates of smaller molecule weight (m/z < 770) by AgBr/Ag3PO4/TiO2. - Abstract: A novel photocatalyst AgBr/Ag3PO4/TiO2 was developed by a simple facile in situ deposition method and used for degradation of mirocystin-LR. TiO2 (P25) as a cost effective chemical was used to improve the stability of AgBr/Ag3PO4 under simulated solar light irradiation. The photocatalytic activity tests for this heterojunction were conducted under simulated solar light irradiation using methyl orange as targeted pollutant. The results indicated that the optimal Ag to Ti molar ratio for the photocatalytic activity of the resulting heterojunction AgBr/Ag3PO4/TiO2 was 1.5 (named as 1.5 BrPTi), which possessed higher photocatalytic capacity than AgBr/Ag3PO4. The 1.5 BrPTi heterojunction was also more stable than AgBr/Ag3PO4 in photocatalysis. This highly efficient and relatively stable photocatalyst was further tested for degradation of the hepatotoxin microcystin-LR (MC-LR). The results suggested that MC-LR was much more easily degraded by 1.5 BrPTi than by AgBr/Ag3PO4. The quenching effects of different scavengers proved that reactive h+ and • OH played important roles for MC-LR degradation
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2014.10.078Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2014.10.078;
- PII
- S0169-4332(14)02317-4;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 325
- Journal Page Range
- p. 1-12
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46113105
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- DEPOSITION; HETEROJUNCTIONS; IRRADIATION; METHYL ORANGE; PHOTOCATALYSIS; QUENCHING; SILVER; SILVER BROMIDES; SILVER PHOSPHATES; SIMULATION; STABILITY; TITANIUM OXIDES; VISIBLE RADIATION
- Descriptors DEC
- AMINES; AZO COMPOUNDS; AZO DYES; BROMIDES; BROMINE COMPOUNDS; CATALYSIS; CHALCOGENIDES; DYES; ELECTROMAGNETIC RADIATION; ELEMENTS; HALIDES; HALOGEN COMPOUNDS; INDICATORS; METALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PHOSPHATES; PHOSPHORUS COMPOUNDS; RADIATIONS; SEMICONDUCTOR JUNCTIONS; SILVER COMPOUNDS; SILVER HALIDES; SULFONIC ACIDS; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.