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http://www.scielo.org.pe/scielo.php?script=sci_arttext&pid=S1810-634X2013000200008
Marilia MS Pupo ; Lucas S. da Costa ; Aíle C. Figueiredo ; Ronaldo S. da
Silva ; Frederico GC Cunha ; Katlin IB Eguiluz ; Giancarlo R. Salazar-Banda
Instituto de Tecnologia e Pesquisa, Programa de Pós-Graduação em
Engenharia de Processos, Universidade Tiradentes, 49032-490 Aracaju-SE,
Brasil
Laboratório de Materiais Cerâmicos Avançados, Departamento de Física,
Universidade Federal de Sergipe, 49100-000 São Cristóvão- SE, Brasil
Departamento de Física, Universidade Federal de Sergipe, CP 353, 49100-
000 São Cristóvão-SE, Brasil
Resumen
Los mejores electrodos basados en SnO2 con mayor actividad electrocatalítica y estabilidad
electroquímica, fueron obtenidos empleando la técnica de precursor polimérico (Pechini)
dopándolos con mayor contenido de rutenio.
RESUMEN
El sólido obtenido por el método de precursor polimérico es amorfo aun para
tratamientos a
350ºC y presenta como principal fase cristalina la anatasa para tratamientos a 450ºC.
A través del análisis con espectroscopia infrarroja, y correlacionando estos datos con
los resultados de DRX, se puede determinar cualitativamente la presencia, en la
muestra,de TiO2 amorfo, con fase anatasa o rutilo a diferentes temperaturas; lo
anterior se justifica con base en la presencia de las bandas características de estos
compuestos en el intervalo de 400 a 1000 cm -1. La forma de las bandas en esta región
se va modificando y se ubicaron bandas, a través del proceso de deconvolución, que se
pueden tomar como referentes para determinar la presencia o no de una cierta fase
cristalina. Así, las bandas ubicadas a ~460, ~510 y ~730 cm-1 se podrían tomar como
características de la fase anatasa y las ubicadas a ~560 y ~670 cm-1 para la fase. Con
base en lo anterior se puede concluir que las muestras tratadas térmicamente a una
temperatura entre 450 y 700ºC presentan una mezcla de anatasa y rutilo; en la
muestra tratada a 700ºC predominaría la fase tipo rutilo.
El método de síntesis utilizado en este trabajo, procedimiento Pechini, permite
obtener TiO2 fase anatasa a 450ºC. Este es un método reproducible que garantiza
características predeterminadas del producto, pequeño tamaño de partícula y buena
pureza química, que lo hacen muy adecuado para diversas aplicaciones tecnológicas
que actualmente se estudian al interior del grupo CYTEMAC.
RESUMEN
Alejandra Montenegro Hernández*, Nathalie Marcela Cerón, Jorge Enrique Rodríguez Páez.
Grupo CYTEMAC. Departamento de Física, Universidad del Cauca, Calle 5
N.° 4-70 Popayán, Colombia.
Rev. Fac. Ing. Univ. Antioquia N.° 44. pp. 43-51. Junio, 2008
(Recibido el 13 de septiembre de 2007. Aceptado el 29 de Enero de 2008)
RESUMEN
De este trabajo se puede concluir lo siguiente:
• Los métodos químicos utilizados, precursor polimérico y precipitación controlada,
permitieron obtener polvos cerámicos del sistema óxido de estaño-óxido de titanio con
tamaño nanométrico, verificado con microscopía electrónica de barrido y transmisión. Se
observa que los sólidos obtenidos tienen un tamaño de partícula primaria menor a 100 nm y
que además es homogéneo. El polvo cerámico sintetizado por precipitación controlada
presentó un alto grado de aglomeración.
• Con base en los resultados de análisis térmico realizado a los polvos cerámicos sintetizados
por el método Pechini, se puede concluir que a partir de 500°C se elimina la parte orgánica y se
cristalizan los óxidos de interés. Para el caso de las muestras obtenidas por precipitación
controlada, por encima de 450°C ocurre un aumento de peso debido a la oxidación del estaño.
La cristalización de la estructura del óxido de estaño, y por lo tanto la formación del SnO2
, es el principal proceso fisicoquímico.
•Los resultados de DRX, para la muestra obtenida por el método del precursor polimérico
(Pechini), indican que el sólido precalcinado a 350°C presenta gran cantidad de fase orgánica
que al tratarla térmicamente a 550°C lleva a la formación de la casiterita como única fase
cristalina (realmente debe corresponder a una solución sólida de SnO2
– TiO2 ). Para el caso de las muestras obtenidas por precipitación controlada, se puede
observar claramente el efecto que tiene la incorporación del óxido de titanio en el sistema: la
muestra que contiene 20% en moles de titanio y varios lavados, presenta como fase cristalina
principal la romarchita SnO, bien cristalizada, mientras que la muestra con 50% en moles de
titanio presenta una mezcla de fases de estaño, casiterita, romarchita y titanio, rutilo. Estos
resultados, junto con los de ATD/TG, indican que mientras en el proceso de precipitación
controlada se favorece la presencia de la romarchita (SnO), por debajo de 450ºC, es muy difícil
obtener un resultado similar utilizando el método del precursor polimérico debido a la etapa
de tratamiento térmico a alta temperatura, aproximadamente 550ºC, a la que se debe
someter la muestra pre-calcinada para obtener la fase estable (solución sólida de SnO2 –
TiO2).
De acuerdo a esto, se vislumbra un método posible, y relativamente sencillo (precipitación
controlada) principalmente para bajas concentraciones de titanio, para sintetizar romarchita,
compuesto que también presenta gran interés tecnológico.
• Todo lo mencionado anteriormente vuelve a poner en evidencia la gran importancia que
tiene el método de síntesis sobre las características estructurales finales que presenta la
materia prima obtenida.
MethodsX
Volume 5, 2018, Pages 1613-1617
RESUMEN
This paper describes a thermal method to obtain metal oxides on a titanium substrate surface.
This adapted Pechini method is a versatile, easy to handle and scalable technique to obtain
electrodes for industrial uses, such as Dimensionally Stable Anodes (DSA). This method has
advantages over other thermal methods like dip coating or sputtering, as it needs a smaller
amount of polymeric mixture than dip coating method to cover the same area and is less
expensive than sputtering method. The thermal method described herein to prepare DSA type
electrodes of RuO2-ZrO2doped with Sb2O5over titanium plates needs no sophisticated
equipment as spray pyrolysis technique does; a muffle, ultrasonic equipment, and a hot plate
magnetic stirrer are the principal apparatus necessary to carry out the adapted Pechini
method. On the other hand, this method allows metal oxides to disperse homogeneously. The
cyclic voltammograms showed the stability of DSA, and the accelerated life test allowed
establishing its useful life (18.18 years) at a current density of 10 mA cm
Shinshu University Shinshu Univ, Fac Text Sci & Technol, Dept Fine Mat Engn, 3-15-1 Tokida,
Ueda, Nagano 3868567, Japan.
The structure of oxide layers of the RuO2-IrO2/Ti electrode system and the thermal decomposition
processes of RuCl3 and IrCl3 to form their respective oxides have been mainly analyzed by EXAFS
(extended X-ray absorption fine structure) and XRD (X-ray diffraction). Upon heating of the
respective chlorides in air, both chlorides convert into their respective oxides. The coordination
numbers of the oxide ions around bath the ruthenium and iridium ions increased with an increase
in the calcination temperature and attained 6, which is the theoretical value of the standard
samples of rutile RuO2 and IrO2. The changes in the coordination number with respect to the
calcination temperature were accompanied by changes in the lattice constants of these oxides. This
suggests that the deviation of these parameters from the standard sample is caused by the lattice
defects of the oxide ions. A dependence of the radial distribution functions of EXAFS on the
composition of the RuO2-IrO2/Ti electrode system showed that RuO2 forms a solid solution with
IrO2 for the binary oxide electrode system.
Shenzhen Angel Drinking Water Ind Grp Corp, Angel Ind Pk, Shenzhen 518108, Guangdong,
Peoples R China.
10, 25952–25957
RESUMEN
This paper reports the pH sensing capability of a ruthenium oxide (RuO2) and iridium oxide
(IrO2) coated titanium (ROIOT) electrode. The characterization results indicated that the ROIOT
electrode had a cracked morphology. The RuO(2)and IrO(2)particles were decorated on the
surface of the electrode. The ROIOT electrode showed near-Nernstian sensitivity of -50.8 mV
pH(-1), with a wide detection range of pH 2-12. The response time was 4.0-13.5 s, which was
fast and very sensitive to the pH change. The ROIOT electrode also demonstrated great
detection reversibility and stability in various pH conditions. In the long-term experiment of 30
d, potential measurements using the ROIOT electrode had a minor fluctuation of 1.5 mV d(-1).
The practical application of the ROIOT electrode was demonstrated by measuring the pH
values of various buffer solutions and complex samples. With the advantages of low cost and
simple production, it is believed that the ROIOT electrode could be a promising candidate for
use as a sensing material for pH sensor development.
Shiraz University of Technology Shiraz Univ Technol, Dept Mat Sci & Engn, Shiraz 71555313,
Iran.
RESUMEN
Recombination of electrons in TiO2 conduction band has detrimental effects on the
performance of dye-sensitized solar cells (DSSCs). Good connection between TiO2
nanoparticles, in meso-porous TiO2 layer, causes a significant reduction in recombination
reaction rate. In the present work, Pechini sol-gel method was used for the synthesis of TiO2
nanoparticle pastes with different amounts of titanium tetra-isopropoxide (TIP) in their sol
precursors. The synthesized paste was used for the fabrication of photoanode of DSSCs. Then,
the effect of TTIP content of sol precursor on the photovoltaic performance of DSSCs was
investigated. For all pastes, the amount of sol in paste was kept constant which led to the
mesa-porous TiO2 layers with the same amount of porosity. Results showed that the
photovoltaic performance of DSSCs first increases and then decreases with increasing TTIP
content of sol precursor. It was concluded that the increase in performance of DSSC is due to
the good connection between TiO2 nanoparticles and the decrease in performance is due to
the micro-cracks in the meso-porous TiO2 layers with high content of TTIP in their sol
precursor. (C) 2014 Elsevier Ltd. All rights reserved .
AUG 2012
Inst Colorants Paint & Coatings, Dept Nanotechnol & Nanomat, Tehran, Iran
RESUMEN
In the current work, titanium dioxide and iron-doped titanium dioxide (0-3%) nanocrystals
were prepared with the Pechini-type sol-gel method. The same procedure as well as spin-
coating technique was applied for preparation of thin films. The prepared samples were
characterised by X-ray diffractometery (XRD) and X-ray photoelectron spectroscopy
techniques. The crystallographic and microstructural parameters of nanopowders were refined
from XRD patterns utilising the Rietveld refinement method. It was found that with
incorporation of iron in TiO2 structure, a highly distorted brookite phase was generated and
the amount of anatase phase was decreased. The rutile phase disappeared with addition of
iron; however, in higher concentration of iron (3%), it reappeared. The results also indicate
that the crystallite size of brookite phase as well as microstrain of anatase and brookite phases
were amplified with iron doping. The results of the photocatalytic test of prepared thin films
are in agreement with the prediction of photocatalytic activity of samples based on their
phase's constituents and structure.
BIBLIOGRAFIA
Coruminas, M., Ronecro, C., Bruguca, E., y Casas, M. (2007). Sistema dopaminérgico y
adicciones, Rev Mukuel, 44(1), 23-31..
Ghghfg
CONCLUSIÓN
In this study, the influence of ionic liquid type on the synthesis of Ti/(RuO2)0.8–(Sb2O4)0.2
electrodes was evaluated. The calcination temperature was also varied during the synthesis
process (500, 550 and 600 °C). The calcination temperature and the ionic liquid type clearly
affected the physical and electrochemical properties of the synthesized electrodes. The coating
of the substrate surface for the electrodes prepared using higher temperatures (600 °C) was
ineffective. In general, electrodes calcined at 550 °C using both ILs showed improved
CONCLUSION
Titanium electrodes covered with ruthenium and antimony oxides with different compositions
(Ti/(RuO2)0.5–(Sb2O5)0.5 and Ti/(RuO2)0.8–(Sb2O5)0.2) were synthesized by using the ionic
liquid (IL) and Pechini methods. These electrodes were characterized by X-ray diffraction,
scanning electron microscopy, energy-dispersive X-ray spectroscopy, and electrochemical
techniques, showing that the electrodes prepared by the IL method (green chemistry route)
presented grains, a noncracked morphology, rutile structure, and significant electroactive area.
The electrocatalytic nature of both electrodes was evaluated by electrochemical degradation
of a persistent organic compound (atrazine herbicide) by applying 10 and 20 mA cm–2, and
compared, for the first time, with a nonactive electrode with higher oxidation power (boron-
doped diamond (BDD)). Results clearly showed that electrodes obtained by the IL method
achieved higher degradation efficiencies. Compared with BDD anode, the Ti/(RuO2)0.8–
(Sb2O5)0.2 electrode showed a similar performance to remove atrazine (98% in 100 min),
EVIDENCING AN IMPROVEMENT IN ITS OXIDATION POWER AS ACTIVE ANODE
Volume 206, 2019 - Issue 5 Pages 647-653 | Received 13 Jan 2018, Accepted 16 Aug 2018,
Published online: 25 Sep 2018
RESUMEN
The modification of carbon felts by the Pechini method resulted in electrochemically stable
CMEs. Materials modified by microwave heating obtained significantly higher values for a
voltam-metric charge (related to the electroactive area) and stability than the bare carbon
felt, whose val- ues were also higher than those of CMEs synthe-sized by conventional
heating. Moreover, the oxide deposition on the fibers improves the con- ductivity of the
CMEs, where microwave pre-pared stands out compared to the conventional. Among all
the CMEs, the highest conductivity is seen for (RuO2)0.9–(Sb2O5)0.05–(Ta2O5)0.05/C.
Microwave heating reduces the CME production time by 60% and produces homogeneous
coatings that maintain the three-dimensional structure of the felts. Thus, the use of
microwave irradiation
Leticia Mirella da Silva , Géssica de Oliveira Santiago Santos, Marilia Moura de Salles Pupo,
Katlin Ivon Barrios Eguiluz, Giancarlo Richard Salazar-Banda,
Journal of Electroanalytical Chemistry 813 (2018) 127–133
CONCLUSION
The present work focused in analysing the influence of cerium doping on the well-known
Sn–SbO2 structure, further studying the different outcomes according to variations in
heating rates and ap- plying ionic liquid in precursor solution preparation. From the results
obtained it is possible to conclude that even the slight variation in heating rates is able to
influence and alter the su- perficial active area of the MMO and consequently its porosity
and electrocatalytic activity. Considering the atomic radius of the metallic elements used,
special care was taken to not overcome cerium amounts in order to achieve proper
incorporation of metal ions, showing that small amounts are able to obtain enhanced
features. The MMO
Electrically conducting adsorbent materials called NyexTM 1000 & 2000 have already been
reported with comparatively low adsorption capacity for various organic, biologically non-
degradable and toxic compounds. Two composite adsorbents called CA1 & CA2 were
synthesized using synthetic graphite carbon black and expanded graphite-carbon black
respectively. The aim of developing the new adsorbents was to increase the adsorption
capacity along with good electrical properties. The develop adsorbents were characterized
using N2 adsorption for specific surface area, Boehm surface titration for surface chemistry,
bed electrical conductivity, laser size analyzer for average particle size, and scanning electron
microscope (SEM) for particle morphology and shape. Then both the composite adsorbents
were tested for the adsorption of acid violet 17 followed by an electrochemical regeneration.
The adsorption study revealed that both the adsorbents had almost similar kinetic behavior
with a significant increase in adsorption capacity for acid violet 17 (300 & 26 mg g1
respectively) when compared with the adsorption capacity of previously developed electrically
conducting materials called NyexTM 1000 & 2000 (3.5 and 9 mg g1 respectively). The
composite adsorbent CA2 was successfully electrochemically regenerated by passing an
electric charge of 138 C g1 at a current density of 14 mA cm2 for a treatment time of 60 min,
whereas, the composite adsorbent CA1 could not be regenerated successfully. The
regeneration efficiencies of CA2 were obtained at around 120% during five adsorption–
regeneration cycles. The amount of actual charge passed of 138 C g1 for achieving 100%
regeneration efficiency was found to be similar with stoichiometrically calculated amount of
charge. The amount of electrical energy required to oxidize each mg of adsorbed acid violet
onto CA2 (24 J mg1) was found to be significantlylower to that of NyexTM 1000 & 2000
adsorbents (52 J mg1 & 32 J mg1 respectively).2013 The Korean Society of Industrial and
Engineering Chemistry. Published by Elsevier B.V. All
REMOVAL OF TYROSOL FROM WATER BY ADSORPTION ON CARBONACEOUS MATERIALS
AND ELECTROCHEMICAL ADVANCED OXIDATION PROCESSES
Nelly Flores , Farbod Sharif , Nael Yasri , Enric Brillas , Ignasi Sires ,Edward P.L. Roberts ,
CONCLUCION
This work compares the ability of physical and chemical treatments, namely adsorption and
electrochemical advanced oxidation processes, to remove tyrosol from aqueous medium.
Adsorption on graphene nanoplatelets (GNPs) performed much better than that with a
graphite intercalation compound. Adsorption isotherms were found to follow the Freundlich
model (R2 1⁄4 0.96), which is characteristic of Achemisorption process. Successful
electrochemical regeneration enables 5 successive adsorption/regeneration cycles before
corrosion of GNPs occurs. Other typical aromatic contaminants that may coexist with tyrosol
can be also adsorbed on GNPs. Percentage of regeneration efficiency of GNPs showed a higher
affinity towards Lewis acids group compounds and a lower one towards Lewis base. The treat-
ment of 100 mL of 0.723 mM tyrosol solutions in non-chlorinated and chlorinated matrices at
pH 3.0 was carried out by electrochemical oxidation with electrogenerated H2O2 (EO-H2O2),
electro-Fenton (EF) and UVA photoelectro-Fenton (PEF). Trials were made with a BDD anode
and an air-diffusion cathode at 10 e30 mA cm2 Hydroxyl radicals formed at the anode from
water oxidation and/or in the bulk from Fenton's reaction between added Fe2þ and generated
H2O2, along with active chlorine produced in chlorinated medium, were the main oxidants.
Tyrosol concentration always decayed following a pseudo-first-order kinetics and its
mineralization rose as EO-H2O2 < EF < PEF, more rapidly in the chlorinated matrix. The potent
photolysis of intermediates under UVA radiation explained the almost total miner- alization
achieved by PEF in the latter medium. The effect of current density and tyrosol content on the
performance of all processes was examined.