Siloxane-based metal–organic frameworks with remarkable catalytic activity in mild environmental photodegradation of azo dyes

[Display omitted] •Synthesis, characterization and catalytic tests of new siloxane-containing MOFs.•Alkaline decomposition of hydrogen peroxide with 90% conversion after 30min.•Unprecedented catalytic activity in photodecomposition of Congo red under sunlight.•Discoloration efficiency of 82% after 8...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2017-05, Vol.205, p.78-92
Hauptverfasser: Racles, Carmen, Zaltariov, Mirela-Fernanda, Iacob, Mihail, Silion, Mihaela, Avadanei, Mihaela, Bargan, Alexandra
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container_start_page 78
container_title Applied catalysis. B, Environmental
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creator Racles, Carmen
Zaltariov, Mirela-Fernanda
Iacob, Mihail
Silion, Mihaela
Avadanei, Mihaela
Bargan, Alexandra
description [Display omitted] •Synthesis, characterization and catalytic tests of new siloxane-containing MOFs.•Alkaline decomposition of hydrogen peroxide with 90% conversion after 30min.•Unprecedented catalytic activity in photodecomposition of Congo red under sunlight.•Discoloration efficiency of 82% after 80min with MOF alone and 97% with H2O2 added.•Cleaner water results when the MOFs are used without addition of H2O2. Three new metal–organic frameworks (MOFs) were obtained from a siloxane dicarboxylic acid (CX), 4,4′-bipyridyne (BPy) or 1,2-bis(4-pyridyl)ethylene (EBPy) and copper or cobalt acetates. The compounds were characterized by IR spectroscopy, powder X-ray diffraction, energy-dispersive X-ray fluorescence (XRF), thermogravimetric analysis (TGA), dynamic water vapor sorption (DVS), electron microscopy (TEM, SEM), UV–vis diffuse reflectance and fluorescence measurements. These hydrophobic MOFs acted as efficient catalysts in two processes occurring in aqueous media. The best result in alkaline decomposition of hydrogen peroxide was 90% conversion after 30min. The catalytic activity in photodecomposition of Congo Red (CR) was followed in mild environmental conditions, i.e. under natural sunlight, without additional oxidation agents or pH adjustments. Unprecedented catalytic activity was found, especially for the Co complex with CX and EBPy, with discoloration efficiency of ca. 82% after 80min of exposure to sunlight. The obtained results, in terms of rate constants and efficiency are comparable with those reported for other catalytic systems in photoreactors or in the presence of H2O2. The best catalyst was also tested in a Fenton-like process and it was found that the addition of H2O2 doubles the rate constant and increases the efficiency to 97%. On the other hand, the remaining waters after CR photodecomposition were analyzed by mass spectrometry (ESI–MS) and it was concluded that “cleaner” water is obtained when the MOFs are used without addition of H2O2.
doi_str_mv 10.1016/j.apcatb.2016.12.034
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Three new metal–organic frameworks (MOFs) were obtained from a siloxane dicarboxylic acid (CX), 4,4′-bipyridyne (BPy) or 1,2-bis(4-pyridyl)ethylene (EBPy) and copper or cobalt acetates. The compounds were characterized by IR spectroscopy, powder X-ray diffraction, energy-dispersive X-ray fluorescence (XRF), thermogravimetric analysis (TGA), dynamic water vapor sorption (DVS), electron microscopy (TEM, SEM), UV–vis diffuse reflectance and fluorescence measurements. These hydrophobic MOFs acted as efficient catalysts in two processes occurring in aqueous media. The best result in alkaline decomposition of hydrogen peroxide was 90% conversion after 30min. The catalytic activity in photodecomposition of Congo Red (CR) was followed in mild environmental conditions, i.e. under natural sunlight, without additional oxidation agents or pH adjustments. Unprecedented catalytic activity was found, especially for the Co complex with CX and EBPy, with discoloration efficiency of ca. 82% after 80min of exposure to sunlight. The obtained results, in terms of rate constants and efficiency are comparable with those reported for other catalytic systems in photoreactors or in the presence of H2O2. The best catalyst was also tested in a Fenton-like process and it was found that the addition of H2O2 doubles the rate constant and increases the efficiency to 97%. On the other hand, the remaining waters after CR photodecomposition were analyzed by mass spectrometry (ESI–MS) and it was concluded that “cleaner” water is obtained when the MOFs are used without addition of H2O2.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/j.apcatb.2016.12.034</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Acetates ; Acetic acid ; Azo dyes ; Azo- dye photodecomposition ; Catalyst ; Catalysts ; Catalytic activity ; Catalytic converters ; Chromium ; Cobalt ; Cobalt acetates ; Cobalt compounds ; Copper compounds ; Decomposition reactions ; Discoloration ; Efficiency ; Electron microscopy ; Environmental conditions ; Ethylene ; Fluorescence ; Hydrogen peroxide ; Hydrogen peroxide decomposition ; Hydrophobicity ; Infrared radiation ; Infrared spectroscopy ; Mass spectrometry ; Mass spectroscopy ; Metals ; MOF ; Oxidation ; pH effects ; Photodecomposition ; Photodegradation ; Powder ; Reagents ; Scanning electron microscopy ; Siloxane ; Siloxanes ; Sorption ; Spectroscopic analysis ; Studies ; Sunlight ; Thermogravimetric analysis ; Transmission electron microscopy ; Water vapor ; X-ray diffraction ; X-ray fluorescence</subject><ispartof>Applied catalysis. 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B, Environmental</title><description>[Display omitted] •Synthesis, characterization and catalytic tests of new siloxane-containing MOFs.•Alkaline decomposition of hydrogen peroxide with 90% conversion after 30min.•Unprecedented catalytic activity in photodecomposition of Congo red under sunlight.•Discoloration efficiency of 82% after 80min with MOF alone and 97% with H2O2 added.•Cleaner water results when the MOFs are used without addition of H2O2. Three new metal–organic frameworks (MOFs) were obtained from a siloxane dicarboxylic acid (CX), 4,4′-bipyridyne (BPy) or 1,2-bis(4-pyridyl)ethylene (EBPy) and copper or cobalt acetates. The compounds were characterized by IR spectroscopy, powder X-ray diffraction, energy-dispersive X-ray fluorescence (XRF), thermogravimetric analysis (TGA), dynamic water vapor sorption (DVS), electron microscopy (TEM, SEM), UV–vis diffuse reflectance and fluorescence measurements. 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B, Environmental</jtitle><date>2017-05-15</date><risdate>2017</risdate><volume>205</volume><spage>78</spage><epage>92</epage><pages>78-92</pages><issn>0926-3373</issn><eissn>1873-3883</eissn><abstract>[Display omitted] •Synthesis, characterization and catalytic tests of new siloxane-containing MOFs.•Alkaline decomposition of hydrogen peroxide with 90% conversion after 30min.•Unprecedented catalytic activity in photodecomposition of Congo red under sunlight.•Discoloration efficiency of 82% after 80min with MOF alone and 97% with H2O2 added.•Cleaner water results when the MOFs are used without addition of H2O2. Three new metal–organic frameworks (MOFs) were obtained from a siloxane dicarboxylic acid (CX), 4,4′-bipyridyne (BPy) or 1,2-bis(4-pyridyl)ethylene (EBPy) and copper or cobalt acetates. The compounds were characterized by IR spectroscopy, powder X-ray diffraction, energy-dispersive X-ray fluorescence (XRF), thermogravimetric analysis (TGA), dynamic water vapor sorption (DVS), electron microscopy (TEM, SEM), UV–vis diffuse reflectance and fluorescence measurements. These hydrophobic MOFs acted as efficient catalysts in two processes occurring in aqueous media. The best result in alkaline decomposition of hydrogen peroxide was 90% conversion after 30min. The catalytic activity in photodecomposition of Congo Red (CR) was followed in mild environmental conditions, i.e. under natural sunlight, without additional oxidation agents or pH adjustments. Unprecedented catalytic activity was found, especially for the Co complex with CX and EBPy, with discoloration efficiency of ca. 82% after 80min of exposure to sunlight. The obtained results, in terms of rate constants and efficiency are comparable with those reported for other catalytic systems in photoreactors or in the presence of H2O2. The best catalyst was also tested in a Fenton-like process and it was found that the addition of H2O2 doubles the rate constant and increases the efficiency to 97%. On the other hand, the remaining waters after CR photodecomposition were analyzed by mass spectrometry (ESI–MS) and it was concluded that “cleaner” water is obtained when the MOFs are used without addition of H2O2.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2016.12.034</doi><tpages>15</tpages></addata></record>
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source ScienceDirect Journals (5 years ago - present)
subjects Acetates
Acetic acid
Azo dyes
Azo- dye photodecomposition
Catalyst
Catalysts
Catalytic activity
Catalytic converters
Chromium
Cobalt
Cobalt acetates
Cobalt compounds
Copper compounds
Decomposition reactions
Discoloration
Efficiency
Electron microscopy
Environmental conditions
Ethylene
Fluorescence
Hydrogen peroxide
Hydrogen peroxide decomposition
Hydrophobicity
Infrared radiation
Infrared spectroscopy
Mass spectrometry
Mass spectroscopy
Metals
MOF
Oxidation
pH effects
Photodecomposition
Photodegradation
Powder
Reagents
Scanning electron microscopy
Siloxane
Siloxanes
Sorption
Spectroscopic analysis
Studies
Sunlight
Thermogravimetric analysis
Transmission electron microscopy
Water vapor
X-ray diffraction
X-ray fluorescence
title Siloxane-based metal–organic frameworks with remarkable catalytic activity in mild environmental photodegradation of azo dyes
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