Showing papers by "Francisco Rodríguez-Reinoso published in 2000"
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TL;DR: In this paper, pyrolysis of two petroleum residues, R1 and R2 of different aromaticities, were studied at 0.1 and 1.0 MPa, 420-480°C, for soak times up to 12 h.
80 citations
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13 Jul 2000
TL;DR: In this article, the authors introduce the reader comprehensively to the sciences of structure of carbons, applications of carbon in nuclear energy, the chemistry of pitch carbonization, the spinnig of carbon fibres, carbon gasification reactions and oxidation protection, mechacnical properties, porosity and adsorption in carbons and coals, with chapters describing coal carbonisation, coal liquefaction and the petrography of coal.
Abstract: Sciences which are used to understand the properties and applications of carbons and graphites need to be described, comprehensively, in book format, at an up-to-date and introductory level. This book introduces the reader, comprehensively, to the sciences of structure of carbons, applications of carbon in nuclear energy, the chemistry of pitch carbonization, the spinnig of carbon fibres, carbon gasification reactions and oxidation protection, mechacnical properties, porosity and adsorption in carbons and coals, with chapters describing coal carbonization, coal liquefaction and the petrography of coal. The book serves both as a textbook and as a reference book and as a text for courses within educational institutions, worldwide.
67 citations
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TL;DR: Activated carbon cloths were prepared from viscous rayon by a two-step activation process (carbonization followed by activation) and a single-stepactivation process (simultaneous carbonization and activation), and were compared in terms of gasification rate, development of porosity and changes in breaking strength.
67 citations
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TL;DR: In this paper, the effect of carbonization conditions on the porosity, mechanical strength and oxygen surface groups of resultant activated carbon cloth is analyzed, in order to optimize the properties of the final product.
57 citations
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TL;DR: In this paper, the phase composition of the different catalysts has been related to the catalytic behavior in the vapour phase hydrogenation of crotonaldehyde (but-2-enal).
Abstract: Alumina- and silica-supported bimetallic Pt–Sn catalysts with different Pt/Sn atomic ratios have
been prepared by using the bimetallic complex cis-[PtCl(SnCl3)(PPh3)2], the monometallic complex cis-[PtCl2(PPh3)2] and SnCl2 as metal precursors. Catalysts have been characterised by X-ray diffraction and transmission electron microscopy techniques, including energy-dispersive X-ray microanalysis, electron diffraction
experiments and lattice-fringe microanalysis. The phase composition of the different catalysts has been
related to the catalytic behaviour in the vapour phase hydrogenation of crotonaldehyde (but-2-enal). Results
show that catalysts containing platinum–tin alloy phases with large particles are more selective towards
the hydrogenation of the carbonyl bond to yield crotyl alcohol. The presence of oxidised tin species on the
surface of the large alloy particles promotes the hydrogenation of the carbonyl bond. In situ diffuse reflectance
infrared spectroscopy studies of crotonaldehyde adsorption under He or H2 reveal differences between bimetallic
catalysts and monometallic, and
these differences
have been related to
the different catalytic behaviour of the catalysts.
52 citations
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TL;DR: In this article, the mesophase formation for three petroleum residues of different aromaticities (R1, R2 and R3) have been followed by optical microscopy (anisotropic content ‘A’) and solvent extraction (insolubility in heptane (HI), toluene (TI), and 1-methyl-2-pyrrolidinone (NMPI).
33 citations
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27 citations
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19 citations
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TL;DR: In this article, an activated carbon-supported cerium dioxide (CeO2/C) has been prepared by impregnation of the support with a solution of cerium (III) nitrate and further decomposition in helium.
Abstract: Activated carbon-supported cerium dioxide (CeO2/C) has been prepared by impregnation of the support with a solution of cerium (III) nitrate and further decomposition in helium. Then, platinum has been deposited on CeO2/C by impregnation with solutions containing H2PtC16 or [Pt(NH3)4](NO3)2. Sample characterisation has been carried out by thermogravimetry (TG), temperature-programmed decomposition (TPD) and reduction (TPR), X-Ray diffraction and temperature-programmed desorption of adsorbed hydrogen (H2-TPD). The interaction between cerium oxide and platinum after different reduction treatments has been checked in two test reactions carried out in the gas phase: hydrogenation of benzene and hydrogenation of crotonaldehyde (2-butenal). Results show that ceria is very well dispersed on the carbon support, this enhancing its interaction with the active metal after high temperature reduction treatments (773 K).
17 citations
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TL;DR: In this paper, multiphase composites based on the Mo-Si-C system have been prepared using a solid-state displacement reaction between Mo2C and Si, which was pelletized under vacuum at 40MPa and heat-treated in argon.
Abstract: The intermetallic compound, MoSi2, has great potential as an elevated-temperature structural material but it exhibits some undesirable properties such as low fracture toughness and low strength at elevated temperatures. Improvement of these properties can be achieved by reinforcing MoSi2 with the addition of SiC particles or whiskers, or by alloying it with Mo5Si3. The preparation of MoSi2 composites from powders gives rise to an oxidation problem since SiO2 covers the raw powder. To avoid this problem, the material must be prepared in situ. In this work, multiphase composites based on the Mo-Si-C system have been prepared using a solid-state displacement reaction between Mo2C and Si. Samples were prepared from a mixture, containing different proportions of Si and Mo2C powders, which was pelletized under vacuum at 40MPa and heat-treated in argon. The pieces obtained exhibit different proportions of SiC, MoSi2 and Mo5Si3. The microhardness obtained ranges from 12 to 14GPa, and Kc is over 8MPa·m1/2, which is higher than that of pieces made of MoSi2 only.
12 citations