Marten In 'T Veld
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Marten In 'T Veld has a total of 56 co-authors. Here are the top co-authors by number of shared publications:
Andres Alastuey
Institute of Environmental Assessment and Water Research, IDAEA-CSIC, 08034 Barcelona, Spain
3 shared publicationsCristina Reche
Institute of Environmental Assessment and Water Research, IDAEA-CSIC, 08034 Barcelona, Spain
3 shared publicationsNoemi Pérez
Institute of Environmental Assessment and Water Research, IDAEA-CSIC, 08034 Barcelona, Spain
3 shared publicationsXavier Querol
Institute of Environmental Assessment and Water Research, IDAEA-CSIC, 08034 Barcelona, Spain
3 shared publicationsA. Alastuey
Institute of Environmental Assessment and Water Research, IDAEA-CSIC, Barcelona 08034, Spain
2 shared publications- Matthew Stanley Johnson
University of Copenhagen (Copenhagen, Denmark)
2 shared publications
Latest Publications
- Open Access
- 25 September 2023
- Published by Elsevier in Science of The Total Environment
- Vol. 906, 167159
Identification of volatile organic compounds and their sources driving ozone and secondary organic aerosol formation in NE Spain
- 25 September 2023
- Published by Elsevier in Science of The Total Environment
- Vol. 906, 167159
Open AccessIdentification of volatile organic compounds and their sources driving ozone and secondary organic aerosol formation in NE Spain
- Open Access
- 21 August 2023
- Published by Elsevier in Science of The Total Environment
- Vol. 902, 166440
Characterizing the sources of ambient PM10 organic aerosol in urban and rural Catalonia, Spain
- 21 August 2023
- Published by Elsevier in Science of The Total Environment
- Vol. 902, 166440
Open AccessCharacterizing the sources of ambient PM10 organic aerosol in urban and rural Catalonia, Spain
- Open Access
- 12 October 2022
- Published by Elsevier in Science of The Total Environment
- Vol. 857 (Pt 2) , 159386
Discovering oxidative potential (OP) drivers of atmospheric PM10, PM2.5, and PM1 simultaneously in North-Eastern Spain
- 12 October 2022
- Published by Elsevier in Science of The Total Environment
- Vol. 857 (Pt 2) , 159386
Open AccessDiscovering oxidative potential (OP) drivers of atmospheric PM10, PM2.5, and PM1 simultaneously in North-Eastern Spain
- Open Access
- 1 November 2021
- Published by Elsevier in Science of The Total Environment
- Vol. 795, 148728
Compositional changes of PM2.5 in NE Spain during 2009–2018: A trend analysis of the chemical composition and source apportionment
- 1 November 2021
- Published by Elsevier in Science of The Total Environment
- Vol. 795, 148728
Open AccessCompositional changes of PM2.5 in NE Spain during 2009–2018: A trend analysis of the chemical composition and source apportionment
- Open Access
- 1 July 2021
- Published by Elsevier in Science of The Total Environment
- Vol. 777, 144579
Understanding the local and remote source contributions to ambient O3 during a pollution episode using a combination of experimental approaches in the Guadalquivir valley, southern Spain
- 1 July 2021
- Published by Elsevier in Science of The Total Environment
- Vol. 777, 144579
Open AccessUnderstanding the local and remote source contributions to ambient O3 during a pollution episode using a combination of experimental approaches in the Guadalquivir valley, southern Spain
- Open Access
- 25 April 2021
- Published by MDPI AG in Sustainability
- Vol. 13 (9) , 4821
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 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.- 25 April 2021
- Published by MDPI AG in Sustainability
- Vol. 13 (9) , 4821
Open AccessFormation 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 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. - Open Access
Novel Materials for Combined Nitrogen Dioxide and Formaldehyde Pollution Control under Ambient Conditions
Formaldehyde (HCHO) and nitrogen dioxide (NO2) often co-exist in urban environments at levels that are hazardous to health. There is a demand for a solution to the problem of their combined removal. In this paper, we investigate catalysts, adsorbents and composites for their removal efficiency (RE) toward HCHO and NO2, in the context of creating a pollution control device (PCD). Proton-transfer-reaction mass spectrometry and cavity ring-down spectrometry are used to measure HCHO, and chemiluminescence and absorbance-based monitors for NO2. Commercially available and lab-synthesized materials are tested under relevant conditions. None of the commercial adsorbents are effective for HCHO removal, whereas two metal oxide-based catalysts are highly effective, with REs of 81 ± 4% and 82 ± 1%, an improvement on previous materials tested under similar conditions. The best performing material for combined removal is a novel composite consisting of a noble metal catalyst supported on a metal oxide, combined with a treated active carbon adsorbent. The composite is theorized to work synergistically to physisorb and oxidize HCHO and chemisorb NO2. It has an HCHO RE of 72 ± 2% and an NO2 RE of 96 ± 2%. This material has potential as the active component in PCDs used to reduce personal pollution exposure.
Open AccessNovel Materials for Combined Nitrogen Dioxide and Formaldehyde Pollution Control under Ambient Conditions
Formaldehyde (HCHO) and nitrogen dioxide (NO2) often co-exist in urban environments at levels that are hazardous to health. There is a demand for a solution to the problem of their combined removal. In this paper, we investigate catalysts, adsorbents and composites for their removal efficiency (RE) toward HCHO and NO2, in the context of creating a pollution control device (PCD). Proton-transfer-reaction mass spectrometry and cavity ring-down spectrometry are used to measure HCHO, and chemiluminescence and absorbance-based monitors for NO2. Commercially available and lab-synthesized materials are tested under relevant conditions. None of the commercial adsorbents are effective for HCHO removal, whereas two metal oxide-based catalysts are highly effective, with REs of 81 ± 4% and 82 ± 1%, an improvement on previous materials tested under similar conditions. The best performing material for combined removal is a novel composite consisting of a noble metal catalyst supported on a metal oxide, combined with a treated active carbon adsorbent. The composite is theorized to work synergistically to physisorb and oxidize HCHO and chemisorb NO2. It has an HCHO RE of 72 ± 2% and an NO2 RE of 96 ± 2%. This material has potential as the active component in PCDs used to reduce personal pollution exposure.