scholarly journals Eco-Friendly Colloidal Aqueous Sol-Gel Process for TiO2 Synthesis: The Peptization Method to Obtain Crystalline and Photoactive Materials at Low Temperature

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 768
Author(s):  
Julien G. Mahy ◽  
Louise Lejeune ◽  
Tommy Haynes ◽  
Stéphanie D. Lambert ◽  
Raphael Henrique Marques Marcilli ◽  
...  

This work reviews an eco-friendly process for producing TiO2 via colloidal aqueous sol–gel synthesis, resulting in crystalline materials without a calcination step. Three types of colloidal aqueous TiO2 are reviewed: the as-synthesized type obtained directly after synthesis, without any specific treatment; the calcined, obtained after a subsequent calcination step; and the hydrothermal, obtained after a specific autoclave treatment. This eco-friendly process is based on the hydrolysis of a Ti precursor in excess of water, followed by the peptization of the precipitated TiO2. Compared to classical TiO2 synthesis, this method results in crystalline TiO2 nanoparticles without any thermal treatment and uses only small amounts of organic chemicals. Depending on the synthesis parameters, the three crystalline phases of TiO2 (anatase, brookite, and rutile) can be obtained. The morphology of the nanoparticles can also be tailored by the synthesis parameters. The most important parameter is the peptizing agent. Indeed, depending on its acidic or basic character and also on its amount, it can modulate the crystallinity and morphology of TiO2. Colloidal aqueous TiO2 photocatalysts are mainly being used in various photocatalytic reactions for organic pollutant degradation. The as-synthesized materials seem to have equivalent photocatalytic efficiency to the photocatalysts post-treated with thermal treatments and the commercial Evonik Aeroxide P25, which is produced by a high-temperature process. Indeed, as-prepared, the TiO2 photocatalysts present a high specific surface area and crystalline phases. Emerging applications are also referenced, such as elaborating catalysts for fuel cells, nanocomposite drug delivery systems, or the inkjet printing of microstructures. Only a few works have explored these new properties, giving a lot of potential avenues for studying this eco-friendly TiO2 synthesis method for innovative implementations.

Catalysts ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1182
Author(s):  
Julien G. Mahy ◽  
Louise Lejeune ◽  
Tommy Haynes ◽  
Nathalie Body ◽  
Simon De Kreijger ◽  
...  

Since the Industrial Revolution, technological advances have generated enormous emissions of various pollutants affecting all ecosystems. The detection and degradation of pollutants has therefore become a critical issue. More than 59 different remediation technologies have already been developed, such as biological remediation, and physicochemical and electrochemical methods. Among these techniques, advanced oxidation processes (AOPs) have been popularized in the treatment of wastewater. The use of ZnO as a photocatalyst for water remediation has been developing fast in recent years. In this work, the goals are to produce ZnO photocatalysts with different morphologies, by using a green sol-gel process, and to study both the influence of the synthesis parameters on the resulting morphology, and the influence of these different morphologies on the photocatalytic activity, for the degradation of an organic pollutant in water. Multiple morphologies were produced (nanotubes, nanorods, nanospheres), with the same crystalline phase (wurtzite). The most important parameter controlling the shape and size was found to be pH. The photoactivity study on a model of pollutant degradation shows that the resulting activity is mainly governed by the specific surface area of the material. A comparison with a commercial TiO2 photocatalyst (Evonik P25) showed that the best ZnO produced with this green process can reach similar photoactivity without a calcination step.


2019 ◽  
Vol 8 (1) ◽  
pp. 266-274 ◽  
Author(s):  
Zhigang Yi ◽  
Qiong Tang ◽  
Tao Jiang ◽  
Ying Cheng

Abstract Hydrophobic silica aerogels (SiO2(AG)) was prepared via sol-gel and solvent exchange method under ambient pressure, which could be transformed to hydrophilic after heated under 500∘C. Heat treatment cannot change its structure. SiO2(AG) samples were the micro-porous structure formed by numerous fine particles and had high specific surface area, pore size and pore volume. The absorption performance of hydrophobic/hydrophilic SiO2(AG) on nitrobenzene, phenol and methylene blue (MB) showed that hydrophobic SiO2(AG) exhibited strong adsorption capacity on slightly soluble organic compounds, while hydrophilic SiO2(AG) was much more effective on adsorbing soluble compounds, which could be analyzed by the hydrophobic and hydrophilic interaction theory between the adsorbent and adsorbate.Hydrophobic/hydrophilic SiO2(AG) adsorption performance for MB is superior to that for phenol, which could be explained via the electrostatic interaction theory.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Azam Marjani ◽  
Reza Khan Mohammadi

AbstractHg(II) has been identified to be one of the extremely toxic heavy metals because of its hazardous effects and this fact that it is even more hazardous to animals than other pollutants such as Ag, Au, Cd, Ni, Pb, Co, Cu, and Zn. Accordingly, for the first time, tetrasulfide-functionalized fibrous silica KCC-1 (TS-KCC-1) spheres were synthesized by a facile, conventional ultrasonic-assisted, sol–gel-hydrothermal preparation approach to adsorb Hg(II) from aqueous solution. Tetrasulfide groups (–S–S–S–S–) were chosen as binding sites due to the strong and effective interaction of mercury ions (Hg(II)) with sulfur atoms. Hg(II) uptake onto TS-KCC-1 in a batch system has been carried out. Isotherm and kinetic results showed a very agreed agreement with Langmuir and pseudo-first-order models, respectively, with a Langmuir maximum uptake capacity of 132.55 mg g–1 (volume of the solution = 20.0 mL; adsorbent dose = 5.0 mg; pH = 5.0; temperature: 198 K; contact time = 40 min; shaking speed = 180 rpm). TS-KCC-1was shown to be a promising functional nanoporous material for the uptake of Hg(II) cations from aqueous media. To the best of our knowledge, there has been no report on the uptake of toxic Hg(II) cations by tetrasulfide-functionalized KCC-1 prepared by a conventional ultrasonic-assisted sol–gel-hydrothermal synthesis method.


Materials ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1554
Author(s):  
Justinas Januskevicius ◽  
Zivile Stankeviciute ◽  
Dalis Baltrunas ◽  
Kęstutis Mažeika ◽  
Aldona Beganskiene ◽  
...  

In this study, an aqueous sol-gel synthesis method and subsequent dip-coating technique were applied for the preparation of yttrium iron garnet (YIG), yttrium iron perovskite (YIP), and terbium iron perovskite (TIP) bulk and thin films. The monophasic highly crystalline different iron ferrite powders have been synthesized using this simple aqueous sol-gel process displaying the suitability of the method. In the next step, the same sol-gel solution was used for the fabrication of coatings on monocrystalline silicon (100) using a dip-coating procedure. This resulted, likely due to substrate surface influence, in all coatings having mixed phases of both garnet and perovskite. Thermogravimetric (TG) analysis of the precursor gels was carried out. All the samples were investigated by X-ray powder diffraction (XRD) analysis. The coatings were also investigated by scanning electron microscopy (SEM), atomic force microscopy (AFM) and Mössbauer spectroscopy. Magnetic measurements were also carried out.


Coatings ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 420
Author(s):  
Giuseppina Raffaini

TiO2 is widely used in biomaterial implants. The topography, chemical and structural properties of titania surfaces are an important aspect to study. The size of TiO2 nanoparticles synthetized by sol–gel method can influence the responses in the biological environment, and by using appropriate heat treatments different contents of different polymorphs can be formed. Protein adsorption is a crucial step for the biological responses, involving, in particular, albumin, the most abundant blood protein. In this theoretical work, using molecular mechanics and molecular dynamics methods, the adsorption process of an albumin subdomain is reported both onto specific different crystallographic faces of TiO2 anatase and also on its ideal three-dimensional nanosized crystal, using the simulation protocol proposed in my previous theoretical studies about the adsorption process on hydrophobic ordered graphene-like or hydrophilic amorphous polymeric surfaces. The different surface chemistry of anatase crystalline faces and the nanocrystal topography influence the adsorption process, in particular the interaction strength and protein fragment conformation, then its biological activity. This theoretical study can be a useful tool to better understand how the surface chemistry, crystal structure, size and topography play a key role in protein adsorption process onto anatase surface so widely used as biomaterial.


Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3876
Author(s):  
Jesús Valdés ◽  
Daniel Reséndiz ◽  
Ángeles Cuán ◽  
Rufino Nava ◽  
Bertha Aguilar ◽  
...  

The effect of microwave radiation on the hydrothermal synthesis of the double perovskite Sr2FeMoO6 has been studied based on a comparison of the particle size and structural characteristics of products from both methods. A temperature, pressure, and pH condition screening was performed, and the most representative results of these are herein presented and discussed. Radiation of microwaves in the hydrothermal synthesis method led to a decrease in crystallite size, which is an effect from the reaction temperature. The particle size ranged from 378 to 318 nm when pH was 4.5 and pressure was kept under 40 bars. According to X-ray diffraction (XRD) results coupled with the size-strain plot method, the product obtained by both synthesis methods (with and without microwave radiation) have similar crystal purity. The Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Spectroscopy (EDS) techniques showed that the morphology and the distribution of metal ions are uniform. The Curie temperature obtained by thermogravimetric analysis indicates that, in the presence of microwaves, the value was higher with respect to traditional synthesis from 335 K to 342.5 K. Consequently, microwave radiation enhances the diffusion and nucleation process of ionic precursors during the synthesis, which promotes a uniform heating in the reaction mixture leading to a reduction in the particle size, but keeping good crystallinity of the double perovskite. Precursor phases and the final purity of the Sr2FeMoO6 powder can be controlled via hydrothermal microwave heating on the first stages of the Sol-Gel method.


2020 ◽  
Vol 43 (1) ◽  
pp. 26-42 ◽  
Author(s):  
Zahra Hajian Karahroudi ◽  
Kambiz Hedayati ◽  
Mojtaba Goodarzi

AbstractThis study presents a preparation of SrFe12O19– SrTiO3 nanocomposite synthesis via the green auto-combustion method. At first, SrFe12O19 nanoparticles were synthesized as a core and then, SrTiO3 nanoparticles were prepared as a shell for it to manufacture SrFe12O19–SrTiO3 nanocomposite. A novel sol-gel auto-combustion green synthesis method has been used with lemon juice as a capping agent. The prepared SrFe12O19–SrTiO3 nanocomposites were characterized by using several techniques to characterize their structural, morphological and magnetic properties. The crystal structures of the nanocomposite were investigated via X-ray diffraction (XRD). The morphology of SrFe12O19– SrTiO3 nanocomposite was studied by using a scanning electron microscope (SEM). The elemental composition of the materials was analyzed by an energy-dispersive X-ray (EDX). Magnetic properties and hysteresis loop of nanopowder were characterized via vibrating sample magnetometer (VSM) in the room temperature. Fourier transform infrared spectroscopy (FTIR) spectra of the samples showed the molecular bands of nanoparticles. Also, the photocatalytic behavior of nanocomposites has been checked by the degradation of azo dyes under irradiation of ultraviolet light.


Materials ◽  
2019 ◽  
Vol 12 (19) ◽  
pp. 3265 ◽  
Author(s):  
Li ◽  
Li ◽  
Li ◽  
Guan ◽  
Zheng ◽  
...  

A new synthesis method for organic–inorganic hybrid Poly(vinylidene fluoride)-SiO2 cation-change membranes (CEMs) is proposed. This method involves mixing tetraethyl orthosilicate (TEOS) and 3-mercapto-propyl-triethoxy-silane (MPTES) into a polyvinylidene fluoride (PVDF) sol-gel solution. The resulting slurry was used to prepare films, which were immersed in 0.01 M HCl, which caused hydrolysis and polycondensation between the MPTES and TEOS. The resulting Si-O-Si polymers chains intertwined and/or penetrated the PVDF skeleton, significantly improving the mechanical strength of the resulting hybrid PVDF-SiO2 CEMs. The -SH functional groups of MPTES oxidized to-SO3H, which contributed to the excellent permeability of these CEMs. The surface morphology, hybrid structure, oxidative stability, and physicochemical properties (IEC, water uptake, membrane resistance, membrane potential, transport number, and selective permittivity) of the CEMs obtained in this work were characterized using scanning electron microscope and Fourier transform infrared spectroscopy, as well as electrochemical testing. Tests to analyze the oxidative stability, water uptake, membrane potential, and selective permeability were also performed. Our organic–inorganic hybrid PVDF-SiO2 CEMs demonstrated higher oxidative stability and lower resistance than commercial Ionsep-HC-C membranes with a hydrocarbon structure. Thus, the synthesis method described in this work is very promising for the production of very efficient CEMs. In addition, the physical and electrochemical properties of the PVDF-SiO2 CEMs are comparable to the Ionsep-HC-C membranes. The electrolysis of the concentrated CoCl2 solution performed using PVDF-SiO2-6 and Ionsep-HC-C CEMs showed that at the same current density, Co2+ production, and current efficiency of the PVDF-SiO2-6 CEM membrane were slightly higher than those obtained using the Ionsep-HC-C membrane. Therefore, our novel membrane might be suitable for the recovery of cobalt from concentrated CoCl2 solutions.


2011 ◽  
Vol 1306 ◽  
Author(s):  
Wenting Dong ◽  
Wendell Rhine ◽  
Greg Caggiano ◽  
Owen R. Evans ◽  
George Gould ◽  
...  

ABSTRACTRefrigeration, air conditioning, and other cooling requirements in buildings, industry, and transportation sectors account for about 10 quads of U.S. primary energy consumption. Therefore, advanced technologies for space cooling in buildings and vehicles – as well as for refrigeration in residential, commercial, and industrial applications – that are more energy efficient, avoid net direct greenhouse gas emissions, reduce lifecycle costs, and can impact large markets are needed. Although current technologies are reaching their efficiency limits, thermoelectric (TE) materials can be used for cooling applications and have potential for significant improvements. Compared to traditional bulk phase TE materials, literature results suggest that nanometer-scale materials allow additional opportunities to improve the efficiency of TE materials. Aerogels are one type of nano-material that offers opportunities to increase the efficiency of TE materials by controlling particle size, particle composition and by reducing the thermal conductivity. Bismuth telluride (Bi2Te3) is the most studied TE material and our objective was to produce bismuth telluride aerogels with controlled microstructures and thermal conductivities to increase the TE figure of merit. Aspen Aerogels developed a novel synthesis method to prepare Bi2Te3 aerogels using the principles of colloidal chemistry and sol-gel chemistry. The reaction conditions were investigated and optimized so that gels could be obtained at low reaction temperatures. The gels were aged and dried using supercritical CO2. The aerogels were characterized by BET, XRD, and SEM. The best aerogels were hot pressed and Seebeck coefficients were determined. The synthetic approach developed and the properties of the aerogels will be presented and compared with Bi2Te3 aerogels and materials prepared by other methods.


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