Abstract:Résumé -Spectroscopie infrarouge en réflexion diffuse (DRIFTS) : application à l'analyse in situ de catalyseurs -La technique infrarouge de spectroscopie de réflexion diffuse (DRIFTS), moins pratiquée que la transmission en raison de ses limitations, est extrêmement utile, en effet indispensable, pour les matériaux non transparents et/ou pour des mesures in situ à la température élevée. Les auteurs décrivent les principes de cette technique et ses avantages par rapport à la spectroscopie infrarouge en transmis… Show more
“…The absorption fraction is easily known from the LambertBeer law. The reflection fraction in the case of infinite thickness (2-3 mm) could be a similar expression to the absorption expression after applying the Kubelka-Munk function (Armaroli et al, 2004). Therefore, the KubelkaMunk conversion leads to a linear relationship between concentration and reflected radiation intensity for DRIFTS spectra.…”
“…Gaining quantitative information from the spectra is non-trivial because the Beer-Lambert law used in transmittance is not applicable in this case. However, Kubelka-Munk theory can be applied to improve the linearity of the dependence of signal intensity upon concentration (Armaroli et al, 2004). The DRIFTS spectrum contains both reflection and absorption signals of incident flux on a particle.…”
Section: Adsorption Of Water On Naclmentioning
confidence: 99%
“…Because it is ease for sample preparation, and it is able to analyze nontransparent materials as well as to make in situ measurement at elevated temperature, in situ diffusion reflectance infrared Fourier transform spectroscopy (DRIFTS) has been demonstrated as a useful technology for surface science and heterogeneous reactions analysis (Fuller and Griffiths, 1978;Armaroli et al, 2004;He et al, 2005). However, the utilization of in situ DRIFTS for the hygroscopic behavior of mineral dusts was little reported.…”
In situ diffusion reflectance infrared Fourier transform spectroscopy was used to study the water adsorption on mineral oxides (SiO 2 , α-Al 2 O 3 , MgO, Fe 2 O 3 , TiO 2 ). The results showed that all the water adsorption isotherms were well fitted with the Brunauer-EmmettTeller (BET)-III type equation, with the calculated monolayers occurring at 24%-30% relative humidity. It showed that about 1-5 layers of water adsorbed on oxides surfaces in ambient relative humidity (20%-90%). The measured deliquescence relative humidity of NaCl was (74 ± 1)%, which demonstrated that DRIFTS is a useful method for the study the hygroscopic behavior of mineral dust. In addition, the limits of DRIFTS were also discussed.
“…The absorption fraction is easily known from the LambertBeer law. The reflection fraction in the case of infinite thickness (2-3 mm) could be a similar expression to the absorption expression after applying the Kubelka-Munk function (Armaroli et al, 2004). Therefore, the KubelkaMunk conversion leads to a linear relationship between concentration and reflected radiation intensity for DRIFTS spectra.…”
“…Gaining quantitative information from the spectra is non-trivial because the Beer-Lambert law used in transmittance is not applicable in this case. However, Kubelka-Munk theory can be applied to improve the linearity of the dependence of signal intensity upon concentration (Armaroli et al, 2004). The DRIFTS spectrum contains both reflection and absorption signals of incident flux on a particle.…”
Section: Adsorption Of Water On Naclmentioning
confidence: 99%
“…Because it is ease for sample preparation, and it is able to analyze nontransparent materials as well as to make in situ measurement at elevated temperature, in situ diffusion reflectance infrared Fourier transform spectroscopy (DRIFTS) has been demonstrated as a useful technology for surface science and heterogeneous reactions analysis (Fuller and Griffiths, 1978;Armaroli et al, 2004;He et al, 2005). However, the utilization of in situ DRIFTS for the hygroscopic behavior of mineral dusts was little reported.…”
In situ diffusion reflectance infrared Fourier transform spectroscopy was used to study the water adsorption on mineral oxides (SiO 2 , α-Al 2 O 3 , MgO, Fe 2 O 3 , TiO 2 ). The results showed that all the water adsorption isotherms were well fitted with the Brunauer-EmmettTeller (BET)-III type equation, with the calculated monolayers occurring at 24%-30% relative humidity. It showed that about 1-5 layers of water adsorbed on oxides surfaces in ambient relative humidity (20%-90%). The measured deliquescence relative humidity of NaCl was (74 ± 1)%, which demonstrated that DRIFTS is a useful method for the study the hygroscopic behavior of mineral dust. In addition, the limits of DRIFTS were also discussed.
“…The peaks at 3765, 3725 and 3672 cm −1 were assigned to terminal, doubly-bridged and triply-bridged OH groups, respectively. The broad peak at 3590 cm −1 has been attributed to hydrogen-bonded OH groups [47,48]. Upon modication with TEOS, a sharp peak centered at 3742 cm −1 appeared, attributed to isolated silanols, considered to be Brønsted acid sites [44,49].…”
A B S T R A C TSilica deposition on the benchmark aqueous phase reforming (APR) catalyst Pt/γ-Al 2 O 3 is studied to prevent or limit hydrolytic attack of the support under hydrothermal APR conditions, for which boehmite formation by support hydration is a known cause for catalyst deactivation. Tetraethyl orthosilicate (TEOS) is employed as a silicon source in a straightforward liquid-phase, silylation process followed by catalyst calcination and reduction. Characterization by X-ray diffraction, temperature-programmed desorption of NH 3 , infrared, 27 Al nuclear magnetic resonance and X-ray photoelectron spectroscopy of the fresh catalysts suggests that silica addition occurs preferentially on the support surface, resulting in weak Brønsted acid sites as well as in the formation of Si-O-Al linkages at the expense of specific surface Lewis acid sites. Silylation and calcination of Pt/γ-Al 2 O 3 causes partial blockage of the metal surface area (12% loss), whereas γ-Al 2 O 3 surface silica modification prior to Pt deposition makes controlled metal deposition difficult. Catalytic performance tests show the overcoated samples to be active in the APR of 5 wt% glycerol, albeit with lower H 2 production rates compared to the benchmark catalyst. Characterization of spent APR catalysts clearly demonstrates that silylation/calcination treatments effectively slows down the transformation of the γ-Al 2 O 3 support due to the formation of a Si-O-Al interface. Overall, the lifetime of the catalyst is increased three-fold as a result of the surface overcoating treatment, with repetitive recycling ultimately leading to loss of the protective silica layer.
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