Browsing by Author "Ribeiro, Filipa"
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- Ball milling modified SAPO-11 based catalysts for n-Decane hydroisomerizationPublication . Ferreira, Luisa; Ribeiro, Filipa; Fernandes, Auguste; Martins, AngelaBifunctional Pt/SAPO-11 catalysts were prepared using as acid matrix the microporous silico-aluminophosphate, SAPO-11, synthesized under microwave radiation. After synthesis, the material was physically modified using a ball mill, changing the grinding time but keeping frequency constant. The metal function (0.5 wt.% Pt) was introduced through mechanical mixture with commercial Pt loaded alumina. The catalysts were characterized by several techniques: powder X-Ray Diffraction, pyridine adsorption followed by infrared spectroscopy, low temperature N-2 adsorption, Hg intrusion porosimetry and electronic microscopy (SEM). The characterization data show modifications of structural and textural properties of the samples as the milling time increases. The catalytic behaviour of Pt/SAPO-11 materials was studied for hydroisomerization of long chain n-alkanes, using n-decane as model molecule, aiming to increase the production of mono-branched isomers. The catalytic results show that, under optimized milling conditions (60 min; 50 Hz) the selectivity into mono-branched isomers increased when compared with parent catalyst.
- Catalytic combustion of toluene on Pt zeolite coated cordierite foamsPublication . Ribeiro, Filipa; Silva, João; Silva, Elisabete; Vaz, M. Fátima; Oliveira, Fernando A. C.The catalytic properties of Pt based cordierite foam catalysts have been evaluated in catalytic combustion of toluene (800 ppm in air). The catalysts contain identical Pt content (0.1%) which was introduced by three different ways: Pt ion exchange on MFI zeolite and then coating on the foam; Pt ion exchange after zeolite coating and finally Pt directly wet impregnated on the cordierite foam. The catalytic behaviour of Pt foam based catalysts was compared with that of PtMFI zeolite under powder form. Pt exchanged MFI supported on the cordierite foams present an improvement of activity for toluene combustion of about 50 degrees C on the light off temperature (T-50%). The enhanced performance of the structured catalysts is due not only to the open structure of foams and homogeneous thin layers catalyst deposited on their cell walls, but also to the fact that the size and location of Pt particles present in MFI zeolite are changed during the dipping step. Indeed, as prepared Pt samples and those used in the preparation of the slurry were observed by transmission electron microscopy revealing that the chemical interaction of PtMFI zeolite with the binder and detergent, both present in the slurry, leads to an increase of Pt particles size which were found to migrate from internal pores to the external surface of zeolite crystallites thereby increasing catalytic activity. (C) 2011 Elsevier B.V. All rights reserved.
- Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-templatePublication . Bertolo, Raquel; Fernandes, Auguste; Ribeiro, Filipa; Silva, João; Martins, Ângela; Ribeiro, Fernando RamoaThe present work deals with preliminary studies concerning a new synthesis approach to prepare SAPO materials with AEL structure and evaluate their catalytic behavior in the hydroisomerization of long paraffins. The new SAPO-11 catalysts were synthesized with the help of a small amine (methylamine, MA) added during the preparation of the initial gel. As MA incorporates into the structure of the final materials, it contributes, together with DPA (dipropylamine), to an increase in Si incorporation as isolated species, which results in Bronsted acid sites. Thus, this new and original synthesis strategy allows to obtain materials with enhanced Bronsted acidity when compared with free MA materials. The catalysts were tested in n-decane hydroisomerization (n-decane was used as a model molecule) and confirmed the effect of MA on the acidic properties of the catalysts. The samples synthesized with MA present a higher number of acid sites that increase the catalytic conversion but have a negative effect in the isomerization selectivity, i.e. a more significant amount of cracking products is formed.
- Incorporation of niobium in SAPO-11 materials: Synthesis and characterizationPublication . Bertolo, Raquel; Martins, Angela; Silva, João; Ribeiro, Filipa; Ribeiro, Fernando Ramoa; Fernandes, AugusteThe present work concerns a new synthesis approach to prepare niobium based SAPO materials with AEL structure and the characterization ofNb species incorporated within the inorganic matrixes. The SAPO-11 materials were synthesized with or without the help of a small amine, methylamine (MA) as co-template, while Nb was added directly during the preparation of the initial gel. Structural, textural and acidic properties of the different supports were evaluated by XRD, TPR, UV-Vis spectroscopy, pyridine adsorption followed by IR spectroscopy and thermal analyses. Pure and well crystalline Nb based SAPO-11 materials were obtained, either with or without MA, using in the initial gel a low Si content of about 0.6. Increasing the Si content of the gel up to 0.9 led to an important decrease of the samples crystallinity. Niobium was found to incorporate the AEL pores support as small Nb2O5 oxide particles and also as extra framework cationic species (Nb5+), compensating the negative charges from the matrix and generating new Lewis acid sites. (C) 2011 Elsevier Inc. All rights reserved.