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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creator | Racles, Carmen Zaltariov, Mirela-Fernanda Iacob, Mihail Silion, Mihaela Avadanei, Mihaela Bargan, Alexandra |
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•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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•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.</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. B, Environmental, 2017-05, Vol.205, p.78-92</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright Elsevier BV May 15, 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-51ae70be101d85a6710aedde758b9b9609959cb379320c2b15c49afc207d946c3</citedby><cites>FETCH-LOGICAL-c371t-51ae70be101d85a6710aedde758b9b9609959cb379320c2b15c49afc207d946c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.apcatb.2016.12.034$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids></links><search><creatorcontrib>Racles, Carmen</creatorcontrib><creatorcontrib>Zaltariov, Mirela-Fernanda</creatorcontrib><creatorcontrib>Iacob, Mihail</creatorcontrib><creatorcontrib>Silion, Mihaela</creatorcontrib><creatorcontrib>Avadanei, Mihaela</creatorcontrib><creatorcontrib>Bargan, Alexandra</creatorcontrib><title>Siloxane-based metal–organic frameworks with remarkable catalytic activity in mild environmental photodegradation of azo dyes</title><title>Applied catalysis. 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. 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><subject>Acetates</subject><subject>Acetic acid</subject><subject>Azo dyes</subject><subject>Azo- dye photodecomposition</subject><subject>Catalyst</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Catalytic converters</subject><subject>Chromium</subject><subject>Cobalt</subject><subject>Cobalt acetates</subject><subject>Cobalt compounds</subject><subject>Copper compounds</subject><subject>Decomposition reactions</subject><subject>Discoloration</subject><subject>Efficiency</subject><subject>Electron microscopy</subject><subject>Environmental conditions</subject><subject>Ethylene</subject><subject>Fluorescence</subject><subject>Hydrogen peroxide</subject><subject>Hydrogen peroxide decomposition</subject><subject>Hydrophobicity</subject><subject>Infrared radiation</subject><subject>Infrared spectroscopy</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Metals</subject><subject>MOF</subject><subject>Oxidation</subject><subject>pH effects</subject><subject>Photodecomposition</subject><subject>Photodegradation</subject><subject>Powder</subject><subject>Reagents</subject><subject>Scanning electron microscopy</subject><subject>Siloxane</subject><subject>Siloxanes</subject><subject>Sorption</subject><subject>Spectroscopic analysis</subject><subject>Studies</subject><subject>Sunlight</subject><subject>Thermogravimetric analysis</subject><subject>Transmission electron microscopy</subject><subject>Water vapor</subject><subject>X-ray diffraction</subject><subject>X-ray fluorescence</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kEtOHDEQhi0UJCaEG7CwlHU3fvTLG6QIJRAJKYvA2qq2q8FDtz2xzcBkA3fIDXMSjCbrrEol_Q_9HyGnnNWc8e5sXcPGQB5rUb6ai5rJ5oCs-NDLSg6D_EBWTImukrKXR-RjSmvGmJBiWJGXn24Oz-CxGiGhpQtmmP--_gnxDrwzdIqw4FOID4k-uXxPIy4QH2CckZZGmHe5iMBkt3V5R52ni5stRb91MfgFfZHQzX3IweJdBAvZBU_DROF3oHaH6RM5nGBOePLvHpPbb19vLq6q6x-X3y--XFdG9jxXLQfs2Yhlrh1a6HrOAK3Fvh1GNaqOKdUqM8peScGMGHlrGgWTEay3qumMPCaf97mbGH49Ysp6HR6jL5WaFw_nXHRNUTV7lYkhpYiT3kRXBu80Z_odtV7rPWr9jlpzoQvqYjvf27As2DqMOhmH3qB1EU3WNrj_B7wBq7SNHA</recordid><startdate>20170515</startdate><enddate>20170515</enddate><creator>Racles, Carmen</creator><creator>Zaltariov, Mirela-Fernanda</creator><creator>Iacob, Mihail</creator><creator>Silion, Mihaela</creator><creator>Avadanei, Mihaela</creator><creator>Bargan, Alexandra</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope><scope>SOI</scope></search><sort><creationdate>20170515</creationdate><title>Siloxane-based metal–organic frameworks with remarkable catalytic activity in mild environmental photodegradation of azo dyes</title><author>Racles, Carmen ; Zaltariov, Mirela-Fernanda ; Iacob, Mihail ; Silion, Mihaela ; Avadanei, Mihaela ; Bargan, Alexandra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-51ae70be101d85a6710aedde758b9b9609959cb379320c2b15c49afc207d946c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acetates</topic><topic>Acetic acid</topic><topic>Azo dyes</topic><topic>Azo- dye photodecomposition</topic><topic>Catalyst</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Catalytic converters</topic><topic>Chromium</topic><topic>Cobalt</topic><topic>Cobalt acetates</topic><topic>Cobalt compounds</topic><topic>Copper compounds</topic><topic>Decomposition reactions</topic><topic>Discoloration</topic><topic>Efficiency</topic><topic>Electron microscopy</topic><topic>Environmental conditions</topic><topic>Ethylene</topic><topic>Fluorescence</topic><topic>Hydrogen peroxide</topic><topic>Hydrogen peroxide decomposition</topic><topic>Hydrophobicity</topic><topic>Infrared radiation</topic><topic>Infrared spectroscopy</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Metals</topic><topic>MOF</topic><topic>Oxidation</topic><topic>pH effects</topic><topic>Photodecomposition</topic><topic>Photodegradation</topic><topic>Powder</topic><topic>Reagents</topic><topic>Scanning electron microscopy</topic><topic>Siloxane</topic><topic>Siloxanes</topic><topic>Sorption</topic><topic>Spectroscopic analysis</topic><topic>Studies</topic><topic>Sunlight</topic><topic>Thermogravimetric analysis</topic><topic>Transmission electron microscopy</topic><topic>Water vapor</topic><topic>X-ray diffraction</topic><topic>X-ray fluorescence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Racles, Carmen</creatorcontrib><creatorcontrib>Zaltariov, Mirela-Fernanda</creatorcontrib><creatorcontrib>Iacob, Mihail</creatorcontrib><creatorcontrib>Silion, Mihaela</creatorcontrib><creatorcontrib>Avadanei, Mihaela</creatorcontrib><creatorcontrib>Bargan, Alexandra</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Applied catalysis. B, Environmental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Racles, Carmen</au><au>Zaltariov, Mirela-Fernanda</au><au>Iacob, Mihail</au><au>Silion, Mihaela</au><au>Avadanei, Mihaela</au><au>Bargan, Alexandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Siloxane-based metal–organic frameworks with remarkable catalytic activity in mild environmental photodegradation of azo dyes</atitle><jtitle>Applied catalysis. 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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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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