Menú secundario

Artículos SCI



2009


M-Doped Al2TiO5 (M=Cr, Mn, Co) Solid Solutions and their Use as Ceramic Pigments


Dondi, M; Lyubenova, TS; Carda, JB; Ocaña, M
Journal of the American Ceramic Society, 92 (2009) 1972-1980
Materiales Coloidales

ABSTRACT

New ceramic pigments based on the tialite (Al2TiO5) structure, doped with Co (pink), Cr (green), or Mn (brown), were prepared through the pyrolysis of aerosols followed by calcination of the obtained powders at 1400°C. The expected decomposition of Al2TiO5 into a mixture of Al2O3 and TiO2 on refiring was inhibited by Cr-doping and also by co-doping with Mg the Mn- or Co-doped samples. Microstructure and phase evolution during pigment preparation were monitored by scanning electron microscopy and XRPD. Unit cell parameters of tialite were determined by Rietveld refinement of the X-ray diffraction patterns, revealing in all cases the formation of solid solutions where the solubility of dopants in the Al2TiO5 lattice followed the trend Co<Mn<Cr. The valence state and possible location of dopants in the tialite lattice were investigated by X-ray photoelectron spectra and diffuse reflectance spectroscopies, which suggested the presence of Cr3+ ions in a large interstitial site of the tialite lattice with a distorted octahedral geometry, and of Mn3+ and Co2+ ions in the Al3+ octahedral sites of the tialite lattice in the former case, and in both Al3+ and Ti4+ octahedral sites in the latter. Testing the ceramic glazes assessed the technological behavior of pigments, which found that the color stability was reasonably good for the Mn-doped tialite and the Cr-doped pigment, although the latter suffered a small loss of green hue. The Co-doped pigment was found to be not stable in glazes, undergoing a cobalt-leaching effect.


Junio, 2009 | DOI: 10.1111/j.1551-2916.2009.03172.x

Fibrous MnO2 Nanoparticles with (2 × 2) Tunnel Structures. Catalytic Activity in the Total Oxidation of Volatile Organic Compounds


Dominguez, MI; Navarro, P; Romero-Sarria, F; Frias, D; Cruz, SA; Delgado, JJ; Centeno, MA; Montes, M; Odriozola, JA
Journal of Nanoscience and Nanotechnology, 9 (2009) 3837-3842
Química de Superficies y Catálisis

ABSTRACT

Manganese oxides having 2 × 2 tunnel structures (cryptomelanes) have been synthesized by a milling method in order to test their efficiency as catalysts for the abatement of volatile organic compounds, using toluene as probe molecule. These materials present excellent textural properties, arising from the nanofiber morphology and were active for toluene total oxidation. DRIFTS of the adsorbed phase allow proposing the role of lattice oxygen in the catalytic reaction.


Junio, 2009 | DOI: 10.1166/jnn.2009.NS76

Chemical Reactions in 2D: Self-Assembly and Self-Esterification of 9(10),16-Dihydroxypalmitic Acid on Mica Surface


Heredia-Guerrero, JA; San-Miguel, MA; Sansom, MSP; Heredia, A; Benitez, JJ
Langmuir, 25 (2009) 6869-6874
Materiales de Diseño para la Energía y Medioambiente

ABSTRACT

9(10),16-Dihydroxypalmitic acid (diHPA) is a particularly interesting polyhydroxylated fatty acid (1) because it is the main monomer of cutin, the most abundant biopolyester in nature, and (2) because the presence of a terminal and a secondary hydroxyl group in midchain positions provides an excellent model to study their intermolecular interactions in a confined phase such as self-assembled layers. In this study we have combined atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), attenuated total reflection Fourier transform infrared (ATR-FT-IR) spectroscopy, as well as molecular dynamics (MD) simulations to conclude that the self-assembling of diHPA molecules on mica is a layer by layer process following a Brunauer−Emmett−Teller (BET) type isotherm and with the first layer growing much faster than the rest. Interactions between secondary hydroxyls reinforce the cohesive energy of the monolayer, while the presence of the terminal hydroxyl group is necessary to trigger the multilayered growth. Besides, XPS and ATR-FT-IR spectroscopies clearly indicate that spontaneous self-esterification occurs upon self-assembling. The esterification reaction is a prerequisite to propose a self-assembly route for the biosynthesis of cutin in nature. Molecular dynamics simulations have shown that internal molecular reorganization within the self-assembled layers provides the appropriate intermolecular orientation to facilitate the nucleophilic attack and the release of a water molecule required by the esterification reaction.


Junio, 2009 | DOI: 10.1021/la9001412

Growth of Crystalline TiO2 by Plasma Enhanced Chemical Vapor Deposition


Borras, A; Sanchez-Valencia, JR; Widmer, R; Rico, VJ; Justo, A; Gonzalez-Elipe, AR
Crystal Growth & Design, 9 (2009) 2868-2876
Nanotecnología en Superficies y Plasma

ABSTRACT

TiO2 thin films in the form of anatase have been prepared by plasma enhanced chemical vapor deposition (PECVD) at 523 K as the substrate temperature and a low working pressure. The study of the microstructure and texture of the films at different stages of deposition show that their growth follows the Kolmogorov’s model developed to describe the evolution of crystalline films from a saturated homogeneous medium. An additional characteristic feature of the growth process by PECVD is the formation of different crystalline domains, particularly at low deposition rates. The effects of this parameter and of the characteristics of the substrate on the growing process are also addressed.


Junio, 2009 | DOI: 10.1021/cg9001779

W,N-Codoped TiO2-Anatase: A Sunlight-Operated Catalyst for Efficient and Selective Aromatic Hydrocarbons Photo-Oxidation


Kubacka, A; Bachiller-Baeza, B; Colon, G; Fernandez-Garcia, M
Journal of Physical Chemistry C, 113 (2009) 8553-8555
Fotocatálisis Heterogénea: Aplicaciones

ABSTRACT

New W,N-doped TiO2 anatase-based materials are synthesized having both unprecedent high activity and selectivity in the gas-phase partial oxidation of aromatic hydrocarbons using sunlight as excitation energy and molecular oxygen as oxidant.


Mayo, 2009 | DOI: 10.1021/jp902618g

Integration of methanol steam reforming and combustion in a microchannel reactor for H2 production: A CFD simulation study


Arzamendi, G; Dieguez, PM; Montes, M; Centeno, MA; Odriozola, JA; Gandia, LM
Catalysis Today, 143 (2009) 25-31
Química de Superficies y Catálisis

ABSTRACT

A computational fluid dynamics (CFD) study of the thermal integration of the steam reforming of methanol (SRM) and the combustion of methanol in a catalytic microchannel reactor is presented. This issue is of interest for in situ H2 production for portable power units based on low-temperature PEM fuel cells. Three-dimensional simulations have been carried out under relevant conditions for the SRM reaction that have shown that microreactors allow achieving complete methanol reforming and combustion at space velocities as high as 50,000 h−1, with selectivities for H2 above 99% at relatively low temperatures in the 270–290 °C range.


Mayo, 2009 | DOI: 10.1016/j.cattod.2008.09.034

Molding with nanoparticle-based one-dimensional photonic crystals: a route to flexible and transferable Bragg mirrors of high dielectric contrast


Calvo, ME; Sobrado, OS; Lozano, G; Miguez, H
Journal of Materials Chemistry, 19 (2009) 3144-3148
Materiales Ópticos Multifuncionales

ABSTRACT

Self-standing, flexible Bragg mirror films of high refractive index contrast and showing intense and wide Bragg peaks are herein presented. Nanoparticle-based one-dimensional photonic crystals are used as templates to infiltrate a polymer, which provides the multilayer with mechanical stability while preserving the dielectric contrast existing in the mold. Such films can be lifted off the substrate and used to coat another surface of arbitrary shape.


Mayo, 2009 | DOI: 10.1039/B902090J

Cationic (V, Mo, Nb, W) doping of TiO2–anatase: A real alternative for visible light-driven photocatalysts


Kubacka, A; Colon, G; Fernandez-Garcia, M
Catalysis Today, 143 (2009) 286-292
Fotocatálisis Heterogénea: Aplicaciones

ABSTRACT

In this article we investigate the structure–activity link of anatase-type Ti–M (M = V, Mo, Nb, and W) mixed oxides used for toluene photo-oxidation under sunlight-type excitation. An analysis of the local and long-range structural and electronic characteristics of the mixed oxides show that only structurally highly homogeneous anatase-type oxides with electronic properties exclusively leading to a band gap decrease drive to efficient visible light-driven photocatalysts. Within our microemulsion preparation method, this only occurs for Ti–V and Ti–W series of samples. The isoelectronic (V4+) substitution of Ti4+ ions at the anatase lattice is characterized by a low solubility limit (ca. 2.5 at. %), and drives to a limited modification of the band gap and to a moderate enhancement of the photo-activity with respect to bare titania reference systems. W presence at anatase cation positions occurs with concomitant presence of cation vacancies derived by the charge imbalance between the W6+ and Ti4+ species. A unique W-vacancy local arrangement is detected by the structural characterization, leading to both an important band gap decrease and enhancement of the photo-activity upon sunlight excitation.


Mayo, 2009 | DOI: 10.1016/j.cattod.2008.09.028

AISI 304 Austenitic stainless steels monoliths for catalytic applications


Martinez, LM; Sanz, O; Dominguez, MI; Centeno, MA; Odriozola, JA
Chemical Engineering Journal, 148 (2009) 191-200
Química de Superficies y Catálisis

ABSTRACT

The thermal treatments of austenitic stainless steels monoliths were studied in order to generate a highly homogeneous and rough oxide scale strongly attached to the base alloy, which will subsequently ensure the good adherence of the catalysts. In this work it has been shown that the morphology, integrity and homogeneity of the scale are strongly influenced by the temperature and time of treatment. Washcoating method was used to deposit on the monolith surface a Au/CeO2 catalyst. The drying procedure turned out to be the most critical variable for the adherence and homogeneity of the catalytic ceria layer, while the ceria colloid concentrations in the starting aqueous dispersion seems to have only a threshold effect. The monolithic reactors containing Au/CeO2 layers are active in the oxidation of CO.


Mayo, 2009 | DOI: 10.1016/j.cej.2008.12.030

High deposition rates of uniform films in tetramethylsilane-based plasmas generated by elementary microwave sources in matrix configuration


Latrasse, L; Lacoste, A; Sanchez-Lopez, JC; Bes, A; Rayar, M; Pelletier, J
Surface and Coatings Technology, 203 (2009) 2343-2349
Materiales Nanoestructurados y Microestructura

ABSTRACT

Plasma scaling up can be achieved by distributing elementary microwave plasma sources on planar rectangular networks. These so-called matrix plasmas can generate uniform sheets of plasma over a wide argon pressure range, from 7.5 to 750 Pa, with densities between 1012 and 1013 cm− 3. In order to estimate the capabilities of matrix plasmas for PACVD processing in terms of deposition rate and uniformity, SiOCH and SiNCH films were deposited using TMS (tetramethylsilane), as the organic gas precursor of silicon, mixed with oxygen or nitrogen flows. Plasmas of O2 / TMS and N2 / TMS gas mixtures can be sustained between 5 and 25 Pa. Variations in the deposition rate as a function of microwave power and nitrogen partial pressure are reported. Thickness uniformity of SiOCH and SiNCH films was measured across a silicon wafer. The obtained deposition rates exceed 1.3 μm/min and the films present a uniformity better than 5% on 75 mm diameter silicon wafers. Composition of the films has also been analyzed by XPS as a function of process parameters: microwave input power, composition of gas mixture, and N2 partial pressure. In particular, these analyses have shown a very low yield of nitrogen incorporation when using N2 gas as nitrogen precursor and high Si and Si–Si bonding contents in the films, probably due to a strong fragmentation of the TMS precursor in the high density plasma.


Mayo, 2009 | DOI: 10.1016/j.surfcoat.2009.02.121

Wetting angles and photocatalytic activities of illuminated TiO2 thin films


Rico, V; Romero, P; Hueso, JL; Espinos, JP; Gonzalez-Elipe, AR
Catalysis Today, 143 (2009) 347-354
Nanotecnología en Superficies y Plasma

ABSTRACT

TiO2 thin films have been prepared by physical vapour deposition (PVD) and plasma enhanced chemical vapour deposition (PECVD) to study the UV-induced photo-activity of this material. Wetting angle variations and photo-catalytic activity for the degradation of dyes upon UV illumination have been compared for thin films with different crystalline structure (amorphous, rutile and anatase), microstructure (columnar, compact, etc.) and porosities as estimated from the values of their refraction indices and their direct assessment with a quartz crystal monitor. The surface of the thin films became superhydrophilic upon UV light irradiation and then it recovered its original state by keeping the samples in the dark. Wetting angle decays follow very similar kinetics for amorphous and crystalline films, independently of their actual porosities. By contrast the photo-catalytic activity was very dependent on the crystalline structure of the films (anatase > rutile > amorphous) and on their porosities. The different behaviour depicted by the films with regard to these two properties suggests that they respond to different though related mechanisms and that they cannot be considered as equivalent when trying to prove the photo-activity of TiO2.


Mayo, 2009 | DOI: 10.1016/j.cattod.2008.09.037

Thermal Stability and Oxidation Resistance of Nanocomposite TiC/a-C Protective Coatings


Martinez-Martinez, D; Lopez-Cartes, C; Gago, R; Fernandez, A; Sanchez-Lopez, JC
Plasma Processes and Polymers, 6 (2009) S462-S467
Materiales Nanoestructurados y Microestructura

ABSTRACT

Nanocomposite films composed by small crystallites of hard phases embedded in an amorphous lubricant matrix have been extensively studied as protective coatings. These kinds of coatings have often to work in extreme environments, exposed to high temperatures (above 800–900 °C), and/or oxidizing/corrosive atmospheres, which may resist. As a result, it is important to study the behavior of such coatings at high temperatures (thermal stability) and in the presence of oxygen (oxidation resistance). In this sense, we have selected a TiC/a-C nanocomposite coating with good mechanical and tribological properties in order to do several thermal tests under three different environments: high vacuum (10−6 mbar), low vacuum (10−1 mbar), and air. Our observations allow us to establish that the film microstructure is stable at least up to 1 000 °C in high vacuum. When oxygen is present, the practical temperature of use is reduced at 700 °C (low partial pressure) and 300 °C (air) by formation of Ti oxides and C removal.


Mayo, 2009 | DOI: 10.1002/ppap.200931002

Molecular dynamics simulation of the effect of pH on the adsorption of rhodamine laser dyes on TiO2 hydroxylated surfaces


Hamad, S; Sanchez-Valencia, JR; Barranco, A; Mejias, JA; Gonzalez-Elipe, AR
Molecular Simulation, 35 (2009) 1140-1151
Nanotecnología en Superficies y Plasma

ABSTRACT

We have carried out a study of adsorption, on the (1 0 1) surface of anatase TiO2, of two industrially relevant rhodamine molecules [rhodamine 6G (R6G) and rhodamine 800 (R800)] employing molecular dynamics. These theoretical studies have shown that R6G must adsorb on surfaces under basic conditions. Moreover, the adsorption of this molecule shows a strong dependence upon the pH of the system, i.e. under basic conditions the adsorption energy is quite high, under neutral conditions the adsorption energy is lower and under acidic conditions an even lower adsorption energy indicates that there must be very little adsorption under such conditions. By contrast, for R800, there is little dependence of the adsorption energy upon the pH, suggesting that the amount of adsorption of these molecules is little affected by this parameter. These theoretical results are in qualitative agreement with the experimental results consisting of the incorporation of these dye molecules into porous thin films.


Mayo, 2009 | DOI: 10.1080/08927020903108083

Study of ground and unground leached vermiculite


Maqueda, C; Perez-Rodriguez, JL; Subrt, J; Murafa, N
Applied Clay Science, 44 (2009) 178-184

ABSTRACT

Grinding of clays modifies their surfaces and can significantly affect their leaching behaviour. The acid reaction of vermiculite from Santa Olalla (Huelva, Spain) with HCl at various concentrations was affected by grinding and acid concentration. The acid leaching of ground vermiculite for 3 min with 1 M HCl solution at 80 °C for 24 h removed MgO and Al2O3 almost completely, leaving a residue containing SiO2 and Fe2O3. X-ray diffraction analysis showed the presence of akaganeite (β-FeOOH) and an amorphous phase (silica). Porosity studies showed a very high specific surface area for ground samples compared with unground vermiculite samples, attributed to the presence of iron in the residue coming from structural iron. High resolution transmission electron microscopy (HRTEM) confirmed the presence of iron oxyhydroxides embedded in the silica material. The particle morphology of the iron oxides corresponded well to akaganeite microcrystals precipitated from solution. The leached vermiculite residue also contained Cl− and a small amount of Ti4+, which were accumulated into the akaganeite microcrystals.


Abril, 2009 | DOI: 10.1016/j.clay.2009.01.019

Tribological carbon-based coatings: An AFM and LFM study


Martinez-Martinez, D; Kolodziejczyk, L; Sanchez-Lopez, JC; Fernandez, A
Surface Science, 603 (2009) 973-979
Materiales Nanoestructurados y Microestructura

ABSTRACT

In this work some carbon-based coatings were studied by atomic force microscopy (AFM) and lateral force microscopy (LFM) techniques in order to evaluate their microstructure and friction properties at the micro and nanoscale. With this aim, four samples were prepared by magnetron sputtering: an amorphous carbon film (a–C), two nanocomposites TiC/a–C with different phase ratio (∼1:1 and ∼1:3) and a nanocrystalline TiC sample. Additionally, a highly oriented pyrolytic graphite (HOPG) and an amorphous hydrogenated carbon coating (a-C:H) were included to help in the evaluation of the influence of the roughness and the hydrogen presence respectively. The topography (roughness) of the samples was studied by AFM, whereas LFM was used to measure the friction properties at the nanoscale by two different approaches. Firstly, an evaluation of possible friction contrast on the samples was done. This task was performed by subtraction of forward and reverse images and lately confirmed by the study of lateral force profiles in both directions and the histograms of the subtraction images. Secondly, an estimation of the average friction coefficient over the analysed surface of each sample was carried out. To take into account the tip evolution/damaging, mica was used as a reference before and after each sample (hereafter called sandwich method), and samples-to-mica friction ratios were calculated. The LFM was shown to be a useful tool to characterise a mixture of phases with different friction coefficients. In general, the friction ratios seemed to be dominated by the amorphous carbon phase, as it was impossible to distinguish among samples with different proportions of the amorphous phase (friction ratios between 1.5 and 1.75). Nevertheless, it could be concluded that the differences in friction behaviour arose from the chemical aspects (nature of the phase and hydrogen content) rather than surface characteristics, since the roughness (Ra values up to 5.7 nm) does not follow the observed trend. Finally, the Ogletree method was employed in order to calibrate the lateral force and estimate the friction coefficient of our samples. A good agreement was found with macroscopic and literature values going from ∼0.3 for TiC to ∼0.1 for pure carbon.


Abril, 2009 | DOI: 10.1016/j.susc.2009.01.043

Synthesis and Characterization of Ce1−xEuxO2−x/2 Mixed Oxides and Their Catalytic Activities for CO Oxidation


Hernandez, WY; Centeno, MA; Romero-Sarria, F; Odriozola, JA
Journal of Physical Chemistry C, 113 (2012) 5629-5635
Química de Superficies y Catálisis

ABSTRACT

A series of Ce1−xEuxO2−x/2 mixed oxides was synthesized by coprecipitation. The solids were characterized by means of XRF, SBET, XRD, UV−vis, and Raman techniques, and their catalytic activities toward CO oxidation were tested. A solid solution, with CeO2 F-type structure, is formed for europium contents (measured as Eu2O3 by XRF) ≤20% wt. For higher contents, the solid solution is not formed, but a physical mixture is detected. The existence of oxygen vacancies in the solids with Eu2O3 contents between 3 and 17% wt was demonstrated by the presence of bands at 532 and 1275 cm−1 in their Raman spectra. The catalytic performances of the solids correlate with the amount of these punctual defects in the solid solution.


Abril, 2009 | DOI: 10.1021/jp8092989

Surface nanostructuring of TiO2 thin films by ion beam irradiation


Romero-Gomez, P; Palmero, A; Yubero, F; Vinnichenko, M; Kolitsch, A; Gonzalez-Elipe, AR
Scripta Materialia, 60 (2009) 574-577
Nanotecnología en Superficies y Plasma

ABSTRACT

This work reports a procedure to modify the surface nanostructure of TiO2 anatase thin films through ion beam irradiation with energies in the keV range. Irradiation with N+ ions leads to the formation of a layer with voids at a depth similar to the ion-projected range. By setting the ion-projected range a few tens of nanometers below the surface of the film, well-ordered nanorods appear aligned with the angle of incidence of the ion beam. Slightly different results were obtained by using heavier (S+) and lighter (B+) ions under similar conditions.


Abril, 2009 | DOI: 10.1016/j.scriptamat.2008.12.014

Sonication induced redox reactions of the Ojén (Andalucía, Spain) vermiculite


Poyato, J; Perez-Rodriguez, JL; Ramirez-Valle, V; Lerf, A; Wagner, FE
Ultrasonics Sonochemistry, 16 (2009) 570-576

ABSTRACT

Sonication in a 1:1 mixture (volume ratio) of water and concentrated H2O2 (30%) is a soft method for particle size reduction of phyllosilicate minerals like vermiculites. Repeated sonication causes a particle size reduction to about 70 nm for the Santa Olalla and to 45 nm for the Ojén-vermiculite. In this context the question arises whether the strong oxidising effect of the hydrogen peroxide affects the oxidation state of the iron in the vermiculites. Therefore, the Fe3+/Fetotal ratio before and after sonication was determined by means of Mössbauer spectroscopy. Whereas this ratio was found to remain almost constant in the Santa Olalla vermiculite, it increased from 0.79 to 0.85 in case of the Ojén sample. In the latter case, the oxidation is accompanied by a decrease of the layer charge.

Surprisingly, sonication in pure water leads to a decrease of the Fe3+/Fetotal ratio in the case of the Ojén-vermiculite, i.e., to an increase of the Fe2+ fraction to roughly twice the value before sonication. Again the Fe3+/Fetotal ratio of the Santa Olalla vermiculite remains unchanged. The surface area SBET of the reduced Ojén-vermiculite amounts to 50 m2/g, which is close to the value obtained in the presence of hydrogen peroxide. The results presented should be taken as a warning that particle size reduction by sonication may be accompanied by a change of the redox state and the layer charge of the material.


Abril, 2009 | DOI: 10.1016/j.ultsonch.2008.12.009

Comparison between micro-Raman and micro-FTIR spectroscopy techniques for the characterization of pigments from Southern Spain Cultural Heritage


Franquelo, ML; Duran, A; Herrera, LK; de Haro, MCJ; Perez-Rodriguez, JL
Journal of Molecular Structure, 924-926 (2009) 404-412

ABSTRACT

An extensive overview of the complementary use of micro-FTIR and micro-Raman spectroscopy in the Cultural Heritage studies is described in this work.

The samples have been prepared using the cross-section technique. This technique allows the examination of a large portion of a single paint layer in its original condition. A variety of pigments from samples belonging principally to the Cultural Heritage of Southern Spain were characterized by micro-Raman spectroscopy using visible excitation sources and micro-FTIR spectroscopy. The pigments studied comprise blue (azurite, ultramarine blue, Prussian blue), red (vermilion, haematite, red ochre, red lead, etc.), ochre and yellow (goethite, orpiment, realgar, etc.), green (malachite, copper resinate), and white (calcite, gypsum, white lead, titanium white, barite, lithopone) pigments, among others. An orientation is given for their appropriate and unequivocal characterization. Characterization by micro-FTIR and micro-Raman presents difficulties with some pigments. In these cases, analysis by EDX solves most of these doubts. The combined use of both spectroscopic techniques, together with SEM–EDX microanalysis, provides one of the most useful methods in the characterization (and possible dating) of materials used in Cultural Heritage.


Abril, 2009 | DOI: 10.1016/j.molstruc.2008.11.041

Co3O4 + CeO2/SiO2 Catalysts for n-Hexane and CO Oxidation


Todorova, S; Kadinov, G; Tenchev, K; Caballero, A; Holgado, JP; Pereniguez, R
Catalysis Letters, 129 (2009) 149-155
Materiales y Procesos Catalíticos de Interés Ambiental y Energético

ABSTRACT

Two-component Co–Ce samples deposited onto SiO2 have been prepared, characterized and tested in the reaction of complete n-hexane and CO oxidation. It was established that cerium enhanced the catalytic activity of cobalt in the reaction of n-hexane oxidation, although this depended on the sequence of cobalt and cerium introduction. Co-impregnation of Co and Ce resulted in a close interaction between Co3O4 and CeO2 leading to more surface oxygen species available and, therefore, a better reactivity.


Abril, 2009 | DOI: 10.1007/s10562-008-9805-x

Páginas

icms