E. Tohfegar; J.S. Moghaddas; E. Sharifzadeh; S. Esmaeilzadeh-Dilmaghani
Abstract
In this work, hydrophobic silica aerogels were synthesized using sol-gel method and drying at ambient pressure. The surface morphology, pore size, and the presence of functional groups on the surface of the nanoparticles were analyzed using FE-SEM, TGA, FT-IR, and EDX, respectively. After calcination ...
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In this work, hydrophobic silica aerogels were synthesized using sol-gel method and drying at ambient pressure. The surface morphology, pore size, and the presence of functional groups on the surface of the nanoparticles were analyzed using FE-SEM, TGA, FT-IR, and EDX, respectively. After calcination at 500 °C, the hydrophilic property of the adsorbents was evaluated by water contact angle measurements. The calcinated silica aerogels were used for adsorption of nitrate from aqueous solution in both batch and continuous processes. In the batch process, the effect of initial nitrate concentration, contact time, pH level, and adsorbent dosage were investigated. Results showed that the nitrate removal percentage increased with the decrement of the pH level and the initial nitrate concentration. On the other hand, increasing the contact time and the adsorbent dosage resulted in higher removal percentage. Accordingly, process optimization resulted in a nitrate removal of 92.2 %. Furthermore, it was found that the equilibrium results were in agreement with the Langmuir isotherm model better than with the Freundlich model and also the adsorption kinetics followed the pseudo-second-order model. In the continuous process, the effects of the input flow rate, the bed height, and the initial nitrate concentration were investigated.
Transport Phenomena,
A. Mohammadi; J. Moghaddas
Volume 16, Issue 1 , March 2019, , Pages 1-21
Abstract
In this study, nanoporous silica aerogel and silica aerogel-activated carbon composites have been synthesized using a water glass precursor by cost effective ambient pressure drying method. Equilibrium and kinetics of benzene and ethyl benzene adsorption on silica aerogel and its composites have been ...
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In this study, nanoporous silica aerogel and silica aerogel-activated carbon composites have been synthesized using a water glass precursor by cost effective ambient pressure drying method. Equilibrium and kinetics of benzene and ethyl benzene adsorption on silica aerogel and its composites have been measured in a batch mode at tree weights of adsorbent. For the first time, the experimental data have been fitted with intra-particle diffusion model for determining of diffusion coefficients. The saturation adsorption capacity of benzene and ethyl benzene vapours was 2033 mg.g-1 and 458 mg.g-1 respectively. The components uptake curves have been described by mathematical models of pseudo first order and pseudo second order models. It has been found that the pseudo first order model fits the experimental data better than the pseudo second order model. Also, the pseudo-second order model could be used for modeling of benzene adsorption over silica aerogel and silica aerogel-2% wt. activated carbon composite at the beginning of adsorption process. The diffusion coefficients of benzene and ethyl benzene within the silica aerogel were in the range of 〖2.16×10〗^(-14) - 〖6.66×10〗^(-13) m2.s-1 and 〖3.65×10〗^(-13) - 〖1.95×10〗^(-12) m2.s-1, respectively.
Process Control and Engineering, Process Safety, HSE
N. Yasrebi; J. Moghaddas
Volume 12, Issue 2 , April 2015, , Pages 3-12
Abstract
> Copper-silica aerogel was synthesized by the sol-gel method and was heated at 400, 500 and 600°C for 3 h in the air. The gained materials were named as sample (a), (b) and (c) respectively. Then all samples were characterized by FE-SEM, EDX and FTIR spectroscopy. For resistance measurements ...
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> Copper-silica aerogel was synthesized by the sol-gel method and was heated at 400, 500 and 600°C for 3 h in the air. The gained materials were named as sample (a), (b) and (c) respectively. Then all samples were characterized by FE-SEM, EDX and FTIR spectroscopy. For resistance measurements the pulverized material was pressed to form a disk-type sensor. The measurements of resistance in the relative humidity range of 11.3-84.3% were performed for all samples. For the following experiments sample (a) was chosen. Then the response time and stability properties were examined. The response time of 7.5 minutes was obtained and the stability graphs showed that in the higher RH the sensor was more stable.