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Dive into the research topics where Silvia Lenaerts is active.

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Featured researches published by Silvia Lenaerts.


Chemosphere | 2003

Catalytic NOx reduction with simultaneous dioxin and furan oxidation

Marcel Goemans; Patrick Clarysse; Joseph Joannès; Petra De Clercq; Silvia Lenaerts; Karel Matthys; Kris Boels

The engineering, construction, performance and running costs of a catalytic flue gas cleaning component in the low dust area of a municipal waste incinerator is discussed. For this purpose, the case study of a Flemish incineration plant is presented, covering the history, the design procedure of the catalyst, relevant process data and the financial aspects. A reliable PCDD/F-destruction by means of oxidation by the catalyst to typical values of 0.001 ng TEQ/Nm3 has been demonstrated. At the same time, NOx- and CO-emissions are reduced by 90% and 20% to about 50 mg/Nm3 and below 10 mg/Nm3, respectively.


Energy and Environmental Science | 2016

CO2 conversion in a dielectric barrier discharge plasma: N2 in the mix as a helping hand or problematic impurity?

R. Snoeckx; S. Heijkers; K. Van Wesenbeeck; Silvia Lenaerts; A. Bogaerts

Carbon dioxide conversion and utilization has gained significant interest over the years. A novel gas conversion technique with great potential in this area is plasma technology. A lot of research has already been performed, but mostly on pure gases. In reality, N2 will always be an important impurity in effluent gases. Therefore, we performed an extensive combined experimental and computational study on the effect of N2 in the range of 1–98% on CO2 splitting in dielectric barrier discharge (DBD) plasma. The presence of up to 50% N2 in the mixture barely influences the effective (or overall) CO2 conversion and energy efficiency, because the N2 metastable molecules enhance the absolute CO2 conversion, and this compensates for the lower CO2 fraction in the mixture. Higher N2 fractions, however, cause a drop in the CO2 conversion and energy efficiency. Moreover, in the entire CO2/N2 mixing ratio, several harmful compounds, i.e., N2O and NOx compounds, are produced in the range of several 100 ppm. The reaction pathways for the formation of these compounds are explained based on a kinetic analysis, which allows proposing solutions on how to prevent the formation of these harmful compounds.


RSC Advances | 2014

Atomic layer deposition-based synthesis of photoactive TiO2 nanoparticle chains by using carbon nanotubes as sacrificial templates

Shaoren Deng; Sammy W. Verbruggen; Zhanbing He; Daire J. Cott; Philippe M. Vereecken; Johan A. Martens; Sara Bals; Silvia Lenaerts; Christophe Detavernier

Highly ordered and self supported anatase TiO2 nanoparticle chains were fabricated by calcining conformally TiO2 coated multi-walled carbon nanotubes (MWCNTs). During annealing, the thin tubular TiO2 coating that was deposited onto the MWCNTs by atomic layer deposition (ALD) was transformed into chains of TiO2 nanoparticles (∼12 nm diameter) with an ultrahigh surface area (137 cm2 per cm2 of substrate), while at the same time the carbon from the MWCNTs was removed. Photocatalytic tests on the degradation of acetaldehyde proved that these forests of TiO2 nanoparticle chains are highly photoactive under UV light because of their well crystallized anatase phase.


Catalysis Science & Technology | 2012

Factors driving the activity of commercial titanium dioxide powders towards gas phase photocatalytic oxidation of acetaldehyde

Sammy W. Verbruggen; Elke Moortgat; Tamas E. Korany; Birger Hauchecorne; Johan A. Martens; Silvia Lenaerts

The photocatalytic activity of two commercial titanium dioxide powders (Cristal Global, Millennium PC500 and Evonik, P25) is compared towards acetaldehyde degradation in the gas phase. In contrast to the extensive literature available, we found a higher activity for the PC500 than for the P25 coating. Here, we present a comprehensive characterization of the bulk and surface properties of both powders. Our comparison shows that the material properties that dominate the overall photocatalytic activity in gas phase differ from those required for the photodegradation of water-borne pollutants.


Journal of Laboratory Automation | 2012

Concept and Validation of a Fully Automated Photocatalytic Test Setup

Tom Tytgat; Birger Hauchecorne; Marianne Smits; Sammy W. Verbruggen; Silvia Lenaerts

Photocatalytic activity can be studied by several methods, each with its own strengths and weaknesses. To study photocatalytic activity in an easy, user-friendly, and realistic way, a completely new setup has been built. The setup is modularly constructed around Fourier transform infrared spectroscopy (FTIR) spectroscopy at the heart of it, resulting in great versatility. Complementary software has been written for automatic control of the setup and for processing the generated data. Two pollutants, oil and n-octane, are tested to validate the performance of the setup. These validation experiments confirm the usefulness and added value of the setup in general and of the FTIR detection methodology as well. It becomes clear that a system of online measurements with good repeatability, accuracy, and user-friendliness has been created.


Chemsuschem | 2011

A Non‐Aqueous Synthesis of TiO2/SiO2 Composites in Supercritical CO2 for the Photodegradation of Pollutants

Jasper Jammaer; Carmela Aprile; Sammy W. Verbruggen; Silvia Lenaerts; Paolo P. Pescarmona; Johan A. Martens

Titania/silica composites with different Ti/Si ratios are synthesized via a nonconventional synthesis route. The synthesis involves non-aqueous reaction of metal alkoxides and formic acid at 75 °C in supercritical carbon dioxide. The as-prepared composite materials contain nanometer-sized anatase crystallites and amorphous silica. Large specific surface areas are obtained. The composites are evaluated in the photocatalytic degradation of phenol in aqueous medium, and in the elimination of acetaldehyde from air. The highest photocatalytic activity in both processes is achieved with a composite containing 40 wt % TiO₂.


Chemical Papers | 2014

Cost-effectiveness analysis to assess commercial TiO2 photocatalysts for acetaldehyde degradation in air

Sammy W. Verbruggen; Tom Tytgat; Steven Van Passel; Johan A. Martens; Silvia Lenaerts

In the commercialisation of photocatalytic air purifiers, the performance as well as the cost of the catalytic material plays an important role. Where most comparative studies only regard the photocatalytic activity as a decisive parameter, in this study both activity and cost are taken into account. Using a cost-effectiveness analysis, six different commercially available TiO2-based catalysts are evaluated in terms of their activities in photocatalytic degradation of acetaldehyde as a model reaction for indoor air purification.


Journal of Vacuum Science and Technology | 2014

Controllable nitrogen doping in as deposited TiO2 film and its effect on post deposition annealing

Shaoren Deng; Sammy W. Verbruggen; Silvia Lenaerts; Johan A. Martens; Sven Van den Berghe; Kilian Devloo-Casier; Wouter Devulder; Jolien Dendooven; Davy Deduytsche; Christophe Detavernier

In order to narrow the band gap of TiO2, nitrogen doping by combining thermal atomic layer deposition (TALD) of TiO2 and plasma enhanced atomic layer deposition (PEALD) of TiN has been implemented. By altering the ratio between TALD TiO2 and PEALD TiN, the as synthesized TiOxNy films showed different band gaps (from 1.91 eV to 3.14 eV). In situ x-ray diffraction characterization showed that the crystallization behavior of these films changed after nitrogen doping. After annealing in helium, nitrogen doped TiO2 films crystallized into rutile phase while for the samples annealed in air a preferential growth of the anatase TiO2 along (001) orientation was observed. Photocatalytic tests of the degradation of stearic acid were done to evaluate the effect of N doping on the photocatalytic activity.


RSC Advances | 2014

Effect of pretreatment and temperature on the properties of Pinnularia biosilica frustules

Erik Van Eynde; Britt Lenaerts; Tom Tytgat; Sammy W. Verbruggen; Birger Hauchecorne; Ronny Blust; Silvia Lenaerts

Diatoms are unicellular microalgae that self-assemble an intricate porous silica cell wall, called frustule. Diatom frustules possess a unique combination of physical and chemical properties (chemical inertness, high mechanical strength, large surface area, low density, good porosity and highly ordered features on the nano-to-micro scale) making diatom frustules suited for many nanotechnological applications. For most proposed applications the organic material covering the frustules needs to be removed. In this paper we investigate the effect of different frustule cleaning methods (drying, autoclavation, SDS/EDTA treatment, H2O2 treatment and HNO3 treatment) and subsequent heat treatment at different temperatures (105 °C, 350 °C, 550 °C and 750 °C) on the material characteristics of the diatom Pinnularia sp. Material characteristics under study are morphology, surface area, pore size, elemental composition and organic content. The cleaned Pinnularia frustules are subsequently investigated as adsorbents to remove methylene blue (MB) from aqueous solution.


ChemPhysChem | 2012

Photocatalytic Removal of Soot: Unravelling of the Reaction Mechanism by EPR and in situ FTIR Spectroscopy

Marianne Smits; Yun Ling; Silvia Lenaerts; Sabine Van Doorslaer

Photocatalytic soot oxidation is studied on P25 TiO(2) as an important model reaction for self-cleaning processes by means of electron paramagnetic resonance (EPR) and Fourier transform infrared (FTIR) spectroscopy. Contacting of carbon black with P25 leads on the one hand to a reduction of the local dioxygen concentration in the powder. On the other hand, the weakly adsorbed radicals on the carbon particles are likely to act as alternative traps for the photogenerated conduction-band electrons. We find furthermore that the presence of dioxygen and oxygen-related radicals is vital for the photocatalytic soot degradation. The complete oxidation of soot to CO(2) is evidenced by in situ FTIR spectroscopy, no intermediate CO is detected during the photocatalytic process.

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Johan A. Martens

Katholieke Universiteit Leuven

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Maarten Keulemans

Katholieke Universiteit Leuven

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Sara Bals

University of Antwerp

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