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Formation of Formaldehyde and Other Byproducts by TiO2 Photocatalyst Materials
Photocatalysts promised to control pollution in an environmentally benign manner, inexpensively, and with a low or cheap energy input. However, the limited chemical activity of photocatalysts has prevented their widespread use. This limitation has two important consequences; in addition to limited r...
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Published in: | Sustainability 2021-05, Vol.13 (9), p.4821 |
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description | Photocatalysts promised to control pollution in an environmentally benign manner, inexpensively, and with a low or cheap energy input. However, the limited chemical activity of photocatalysts has prevented their widespread use. This limitation has two important consequences; in addition to limited removal efficiency for pollution, photocatalysts may also generate unwanted byproducts due to incomplete reaction. This study focuses on the byproducts formed in the photocatalytic degradation of dimethyl sulfide (DMS) on titanium dioxide (TiO2), using a continuous flow reactor and detection via proton transfer reaction mass spectrometry. TiO2, activated carbon (AC), TiO2/AC (1:1) and TiO2/AC (1:5) were tested using either a laser-driven light source or LED lamps at 365 nm. The samples were characterized using a N2-BET surface area and pore size distributions, Scanning Electron Microscopy, X-ray Diffraction, and X-ray Photoelectron Spectroscopy, which confirmed that TiO2 was successfully coated on activated carbon without unexpected phases. TiO2 and activated carbon showed different removal mechanisms for DMS. The maximum yield of formaldehyde, 11.4%, was observed for DMS reacting on a TiO2/AC (1:5) composite operating at a DMS removal efficiency of 31.7% at 50 ∘C. In addition to formaldehdye, significant products included acetone and dimethyl disulfide. In all, observed byproducts accounted for over half of the DMS material removed from the airstream. The TiO2/AC (1:5) and TiO2/AC (1:1) composites have a lower removal efficiency than TiO2, but a higher yield of byproducts. Experiments conducted from 20 ∘C to 70 ∘C showed that as temperature increases, the removal efficiency decreases and the production of byproducts increases even more. This is attributed both to decreased surface activity at high temperatures due to increased recombination of reactive species, and to the decreased residence time of volatile compounds on a hot surface. This study shows that potentially dangerous byproducts are formed by photocatalytic reactors because the reaction is incomplete under the conditions generally employed. |
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However, the limited chemical activity of photocatalysts has prevented their widespread use. This limitation has two important consequences; in addition to limited removal efficiency for pollution, photocatalysts may also generate unwanted byproducts due to incomplete reaction. This study focuses on the byproducts formed in the photocatalytic degradation of dimethyl sulfide (DMS) on titanium dioxide (TiO2), using a continuous flow reactor and detection via proton transfer reaction mass spectrometry. TiO2, activated carbon (AC), TiO2/AC (1:1) and TiO2/AC (1:5) were tested using either a laser-driven light source or LED lamps at 365 nm. The samples were characterized using a N2-BET surface area and pore size distributions, Scanning Electron Microscopy, X-ray Diffraction, and X-ray Photoelectron Spectroscopy, which confirmed that TiO2 was successfully coated on activated carbon without unexpected phases. TiO2 and activated carbon showed different removal mechanisms for DMS. The maximum yield of formaldehyde, 11.4%, was observed for DMS reacting on a TiO2/AC (1:5) composite operating at a DMS removal efficiency of 31.7% at 50 ∘C. In addition to formaldehdye, significant products included acetone and dimethyl disulfide. In all, observed byproducts accounted for over half of the DMS material removed from the airstream. The TiO2/AC (1:5) and TiO2/AC (1:1) composites have a lower removal efficiency than TiO2, but a higher yield of byproducts. Experiments conducted from 20 ∘C to 70 ∘C showed that as temperature increases, the removal efficiency decreases and the production of byproducts increases even more. This is attributed both to decreased surface activity at high temperatures due to increased recombination of reactive species, and to the decreased residence time of volatile compounds on a hot surface. This study shows that potentially dangerous byproducts are formed by photocatalytic reactors because the reaction is incomplete under the conditions generally employed.</description><identifier>ISSN: 2071-1050</identifier><identifier>EISSN: 2071-1050</identifier><identifier>DOI: 10.3390/su13094821</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acetone ; Activated carbon ; Air pollution ; Byproducts ; Chemical activity ; Chromatography ; Continuous flow ; Dimethyl sulfide ; Efficiency ; High temperature ; Hot surfaces ; Humidity ; Indoor air quality ; Light ; Light emitting diodes ; Light sources ; Mass spectrometry ; Mass spectroscopy ; Oxidation ; Photocatalysis ; Photocatalysts ; Photodegradation ; Photoelectron spectroscopy ; Photoelectrons ; Pollutant removal ; Pollutants ; Pollution ; Pollution control ; Pore size ; Reactors ; Recombination ; Scanning electron microscopy ; Scientific imaging ; Sustainability ; Titanium dioxide ; VOCs ; Volatile compounds ; Volatile organic compounds ; X-ray diffraction</subject><ispartof>Sustainability, 2021-05, Vol.13 (9), p.4821</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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However, the limited chemical activity of photocatalysts has prevented their widespread use. This limitation has two important consequences; in addition to limited removal efficiency for pollution, photocatalysts may also generate unwanted byproducts due to incomplete reaction. This study focuses on the byproducts formed in the photocatalytic degradation of dimethyl sulfide (DMS) on titanium dioxide (TiO2), using a continuous flow reactor and detection via proton transfer reaction mass spectrometry. TiO2, activated carbon (AC), TiO2/AC (1:1) and TiO2/AC (1:5) were tested using either a laser-driven light source or LED lamps at 365 nm. The samples were characterized using a N2-BET surface area and pore size distributions, Scanning Electron Microscopy, X-ray Diffraction, and X-ray Photoelectron Spectroscopy, which confirmed that TiO2 was successfully coated on activated carbon without unexpected phases. TiO2 and activated carbon showed different removal mechanisms for DMS. The maximum yield of formaldehyde, 11.4%, was observed for DMS reacting on a TiO2/AC (1:5) composite operating at a DMS removal efficiency of 31.7% at 50 ∘C. In addition to formaldehdye, significant products included acetone and dimethyl disulfide. In all, observed byproducts accounted for over half of the DMS material removed from the airstream. The TiO2/AC (1:5) and TiO2/AC (1:1) composites have a lower removal efficiency than TiO2, but a higher yield of byproducts. Experiments conducted from 20 ∘C to 70 ∘C showed that as temperature increases, the removal efficiency decreases and the production of byproducts increases even more. This is attributed both to decreased surface activity at high temperatures due to increased recombination of reactive species, and to the decreased residence time of volatile compounds on a hot surface. This study shows that potentially dangerous byproducts are formed by photocatalytic reactors because the reaction is incomplete under the conditions generally employed.</description><subject>Acetone</subject><subject>Activated carbon</subject><subject>Air pollution</subject><subject>Byproducts</subject><subject>Chemical activity</subject><subject>Chromatography</subject><subject>Continuous flow</subject><subject>Dimethyl sulfide</subject><subject>Efficiency</subject><subject>High temperature</subject><subject>Hot surfaces</subject><subject>Humidity</subject><subject>Indoor air quality</subject><subject>Light</subject><subject>Light emitting diodes</subject><subject>Light sources</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Oxidation</subject><subject>Photocatalysis</subject><subject>Photocatalysts</subject><subject>Photodegradation</subject><subject>Photoelectron spectroscopy</subject><subject>Photoelectrons</subject><subject>Pollutant removal</subject><subject>Pollutants</subject><subject>Pollution</subject><subject>Pollution control</subject><subject>Pore size</subject><subject>Reactors</subject><subject>Recombination</subject><subject>Scanning electron microscopy</subject><subject>Scientific imaging</subject><subject>Sustainability</subject><subject>Titanium dioxide</subject><subject>VOCs</subject><subject>Volatile compounds</subject><subject>Volatile organic compounds</subject><subject>X-ray diffraction</subject><issn>2071-1050</issn><issn>2071-1050</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpNkM1LAzEQxYMoWGov_gUBb8LqTKb7ddTiF1TroZ6XNJnQLW1Tk-xh_3tXK-hcfvNgmPd4Qlwi3BDVcBs7JKinlcITMVJQYoaQw-m__VxMYtzAMERYYzESb48-7HRq_V56J3_E1vK6tyz13spFWnOQ9_0heNuZFOWql8t2oeT72idvdNLbPib5qhOHVm_jhThzA3jyy7H4eHxYzp6z-eLpZXY3z4yq85RRzisuwRpDxhmqnONcVwWQKp3RpZ2WFhEsVUZRpYk5N1qjXVlkhaUDGour498h2GfHMTUb34X9YNmonACLAgaOxfXxygQfY2DXHEK706FvEJrvypq_yugLPdBemw</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Yu, Weijia</creator><creator>in `t Veld, Marten</creator><creator>Bossi, Rossana</creator><creator>Ateia, Mohamed</creator><creator>Tobler, Dominique</creator><creator>Feilberg, Anders</creator><creator>Bovet, Nicolas</creator><creator>Johnson, Matthew S.</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>4U-</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0001-5153-8810</orcidid><orcidid>https://orcid.org/0000-0002-5081-0517</orcidid><orcidid>https://orcid.org/0000-0002-3645-3955</orcidid><orcidid>https://orcid.org/0000-0001-5807-1336</orcidid><orcidid>https://orcid.org/0000-0001-8532-1855</orcidid><orcidid>https://orcid.org/0000-0002-6396-7222</orcidid><orcidid>https://orcid.org/0000-0002-3524-5513</orcidid></search><sort><creationdate>20210501</creationdate><title>Formation of Formaldehyde and Other Byproducts by TiO2 Photocatalyst Materials</title><author>Yu, Weijia ; 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However, the limited chemical activity of photocatalysts has prevented their widespread use. This limitation has two important consequences; in addition to limited removal efficiency for pollution, photocatalysts may also generate unwanted byproducts due to incomplete reaction. This study focuses on the byproducts formed in the photocatalytic degradation of dimethyl sulfide (DMS) on titanium dioxide (TiO2), using a continuous flow reactor and detection via proton transfer reaction mass spectrometry. TiO2, activated carbon (AC), TiO2/AC (1:1) and TiO2/AC (1:5) were tested using either a laser-driven light source or LED lamps at 365 nm. The samples were characterized using a N2-BET surface area and pore size distributions, Scanning Electron Microscopy, X-ray Diffraction, and X-ray Photoelectron Spectroscopy, which confirmed that TiO2 was successfully coated on activated carbon without unexpected phases. TiO2 and activated carbon showed different removal mechanisms for DMS. The maximum yield of formaldehyde, 11.4%, was observed for DMS reacting on a TiO2/AC (1:5) composite operating at a DMS removal efficiency of 31.7% at 50 ∘C. In addition to formaldehdye, significant products included acetone and dimethyl disulfide. In all, observed byproducts accounted for over half of the DMS material removed from the airstream. The TiO2/AC (1:5) and TiO2/AC (1:1) composites have a lower removal efficiency than TiO2, but a higher yield of byproducts. Experiments conducted from 20 ∘C to 70 ∘C showed that as temperature increases, the removal efficiency decreases and the production of byproducts increases even more. This is attributed both to decreased surface activity at high temperatures due to increased recombination of reactive species, and to the decreased residence time of volatile compounds on a hot surface. This study shows that potentially dangerous byproducts are formed by photocatalytic reactors because the reaction is incomplete under the conditions generally employed.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/su13094821</doi><orcidid>https://orcid.org/0000-0001-5153-8810</orcidid><orcidid>https://orcid.org/0000-0002-5081-0517</orcidid><orcidid>https://orcid.org/0000-0002-3645-3955</orcidid><orcidid>https://orcid.org/0000-0001-5807-1336</orcidid><orcidid>https://orcid.org/0000-0001-8532-1855</orcidid><orcidid>https://orcid.org/0000-0002-6396-7222</orcidid><orcidid>https://orcid.org/0000-0002-3524-5513</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetone Activated carbon Air pollution Byproducts Chemical activity Chromatography Continuous flow Dimethyl sulfide Efficiency High temperature Hot surfaces Humidity Indoor air quality Light Light emitting diodes Light sources Mass spectrometry Mass spectroscopy Oxidation Photocatalysis Photocatalysts Photodegradation Photoelectron spectroscopy Photoelectrons Pollutant removal Pollutants Pollution Pollution control Pore size Reactors Recombination Scanning electron microscopy Scientific imaging Sustainability Titanium dioxide VOCs Volatile compounds Volatile organic compounds X-ray diffraction |
title | Formation of Formaldehyde and Other Byproducts by TiO2 Photocatalyst Materials |
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