Fabricating iron-cobalt layered double hydroxide derived from metal-organic framework for the activation of peroxymonosulfate towards tetracycline degradation
Creators
- 1. College of Environmental Science and Engineering, Hunan University and Key Laboratory of Environmental Biology and Pollution Control, Ministry of Education, Hunan University, Changsha, 410082 (China)
- 2. Hunan Dalu Technol Co Ltd, 559 Yunxi Rd, Changsha, 410036, Hunan (China)
- 3. Science and Technology Service Center of Hunan Province, Changsha, 410128 (China)
- 4. College of Resources and Environment, Key Laboratory of Agricultural Environment, Shandong Agricultural University, Tai'an, 271000 (China)
- 5. Hunan Xinheng Environmental Technology Co Ltd, Changsha, 410005 (China)
Description
Highlights: • FeCo-LDH was prepared by sacrificing ZIF-67 templates in Fe3+ ethanolic solution. • FeCo-LDH can efficiently degrade tetracycline (TC) by activating PMS. • SO4.• - and O2• - radicals were the main reactive species in FeCo-LDH/PMS system. • FeCo-LDH catalyst exhibited high removal efficiency after three recycle test. • The FeCo-LDH/PMS system keep high efficiency in actual water. Herein, iron-cobalt layered double hydroxide (FeCo-LDH) was synthesized by sacrificing Co-containing zeolite imidazolate framework materials (ZIF-67) in iron ethanolic solution at room temperature. The catalytic performances of catalysts were investigated by activating peroxymonosulfate (PMS) for tetracycline (TC) degradation. Experimental results were demonstrated that FeCo-LDH with molar ratios of Fe and Co was 1.5 (FeCo-LDH-1.5) exhibited the highest catalytic activity, in which the TC degradation efficiency was reached to 92% within 5min. The system of FeCo-LDH-1.5/PMS exhibited high stability and high efficiency in the influencing factor experiments including TC concentrations, initial pH, coexisting anions (Na+, Cl-, SO42−) and humic acid (HA). Results of quenching experiments and electron paramagnetic resonance (EPR) characterization showed that O2• - and SO4• - radicals were the foremost reactive species for TC degradation. Liquid chromatograph - mass spectrometer (LC-MS) and three-dimensional excitation emission matrix fluorescence spectro photometer (3D EEMs) were conducted to investigate the degradation intermediate and possible degradation pathway. Moreover, high degradation efficiency was implemented in actual wastewater by the FeCo-LDH-1.5/PMS system. Compared to Fe3+/PMS and Co2+/PMS homogeneous system, the FeCo-LDH-1.5/PMS system was exhibited advantages in catalytic activity and high reusability. This study provided a convenient method to synthesis advanced hydrotalcite-like catalysts, which showed remarkable performance in actual wastewater treatment.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jssc.2020.121857Additional details
Identifiers
- DOI
- 10.1016/j.jssc.2020.121857;
- PII
- S0022459620306885;
Publishing Information
- Journal Title
- Journal of Solid State Chemistry (Print)
- Journal Volume
- 294
- Journal Page Range
- vp.
- ISSN
- 0022-4596
- CODEN
- JSSCBI
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54024523
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ANIONS; CATALYSTS; CHLORINE IONS; COMPARATIVE EVALUATIONS; EFFICIENCY; ELECTRON SPIN RESONANCE; EXCITATION; FLUORESCENCE; HYDROXIDES; IRON IONS; LIQUIDS; RADICALS; SOLUTIONS; SULFATES; WASTE WATER; ZEOLITES
- Descriptors DEC
- CHARGED PARTICLES; DISPERSIONS; EMISSION; ENERGY-LEVEL TRANSITIONS; EVALUATION; FLUIDS; HOMOGENEOUS MIXTURES; HYDROGEN COMPOUNDS; INORGANIC ION EXCHANGERS; ION EXCHANGE MATERIALS; IONS; LIQUID WASTES; LUMINESCENCE; MAGNETIC RESONANCE; MATERIALS; MINERALS; MIXTURES; OXYGEN COMPOUNDS; PHOTON EMISSION; RESONANCE; SILICATE MINERALS; SULFUR COMPOUNDS; WASTES; WATER
Optional Information
- Copyright
- Copyright (c) 2020 Elsevier Inc. All rights reserved.