scholarly journals Synthesis of Diatomite-Based Mesoporous Wool-Ball-Like Microspheres and Their Application for Toluene Total Oxidation Reaction

Nanomaterials ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 339
Author(s):  
Quoc-Chon Le ◽  
Chinh Chien Nguyen ◽  
Thi Thanh Nhi Le ◽  
Thierry Lefèvre ◽  
Minh Tuan Nguyen Dinh ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Hydrothermal Treatment ◽  
Specific Surface Area ◽  
Oxidation Reaction ◽  
Cetyltrimethylammonium Bromide ◽  
Low Cost ◽  
Total Oxidation ◽  
Mesoporous Microspheres ◽  
Toluene Total Oxidation

Diatomite (DE) has attracted considerable attention owing to its abundance, low cost, and potential for a wide variety of applications. This work reports the development of mesoporous wool-ball-like (WBL) microspheres from natural DE through a simple hydrothermal treatment. We discovered that the presence of cetyltrimethylammonium bromide is a prerequisite for generating monodispersed WBL microspheres. The mechanism for the transformation of pristine DE into mesoporous microspheres through dissolution–recrystallization was clearly investigated. Interestingly, the microspheres exhibited a specific surface area 25–60 times larger than that of the pristine DE. The application of WBL microsphere DE as an effective support for metallic catalysts in the toluene total oxidation reaction was demonstrated.

scholarly journals Nanocomposite Materials Based on Electrochemically Synthesized Graphene Polymers: Molecular Architecture Strategies for Sensor Applications

Chemosensors ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 149
Author(s):  
André Olean-Oliveira ◽  
Gilberto A. Oliveira Brito ◽  
Celso Xavier Cardoso ◽  
Marcos F. S. Teixeira
Keyword(s):  
Conducting Polymers ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Electrochemical Sensors ◽  
Structural Characteristics ◽  
Low Cost ◽  
Large Specific Surface Area ◽  
Molecular Architecture ◽  
Sensor Applications

The use of graphene and its derivatives in the development of electrochemical sensors has been growing in recent decades. Part of this success is due to the excellent characteristics of such materials, such as good electrical and mechanical properties and a large specific surface area. The formation of composites and nanocomposites with these two materials leads to better sensing performance compared to pure graphene and conductive polymers. The increased large specific surface area of the nanocomposites and the synergistic effect between graphene and conducting polymers is responsible for this interesting result. The most widely used methodologies for the synthesis of these materials are still based on chemical routes. However, electrochemical routes have emerged and are gaining space, affording advantages such as low cost and the promising possibility of modulation of the structural characteristics of composites. As a result, application in sensor devices can lead to increased sensitivity and decreased analysis cost. Thus, this review presents the main aspects for the construction of nanomaterials based on graphene oxide and conducting polymers, as well as the recent efforts made to apply this methodology in the development of sensors and biosensors.

The Effect of Hydrothermal Treatment on Samaria and Gadolinia Doped Ceria Powders Synthesized by Coprecipitation

2010 ◽  
Vol 660-661 ◽  
pp. 959-964
Author(s):  
Alexander Rodrigo Arakaki ◽  
Walter Kenji Yoshito ◽  
Valter Ussui ◽  
Dolores Ribeiro Ricci Lazar
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Hydrothermal Treatment ◽  
Specific Surface Area ◽  
Gas Adsorption ◽  
Fluorite Structure ◽  
High Specific Surface Area ◽  
Powder Synthesis ◽  
Laser Scattering ◽  
The One

One of the main applications of ceria-based (CeO2) ceramics is the manufacturing of Intermediate Temperature Solid Oxide Fuel Cells electrolytes. In order to improve ionic conductivity and densification of these materials various powder synthesis routes have been studied. In this work powders with composition Ce0.8(SmGd)0.2O1.9 have been synthesized by coprecipitation and hydrothermal treatment. A concentrate of rare earths containing 90wt% of CeO2 and other containing 51% of Sm2O3 and 30% of Gd2O3, both prepared from monazite processing, were used as precursor materials. The powders were characterized by X-ray diffraction, scanning and transmission electron microscopy, agglomerate size distribution by laser scattering and specific surface area by gas adsorption. Ceramic sinterability was evaluated by dilatometry and density measurements by Archimedes method. High specific surface area powders (~100m2/g) and cubic fluorite structure were obtained after hydrothermal treatment around 200°C. Ceramic densification was improved when compared to the one prepared from powders calcined at 800°C.

Synthesis of Novel Core-Shell Structured Hydroxyapatite/Meso-Silica for Removal of Methylene Blue from Aqueous Solutions

2012 ◽  
Vol 463-464 ◽  
pp. 543-547 ◽  
Author(s):  
Cheng Feng Li ◽  
Xiao Lu Ge ◽  
Shu Guang Liu ◽  
Fei Yu Liu
Keyword(s):  
Methylene Blue ◽  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Low Cost ◽  
Nitrogen Adsorption ◽  
Precipitation Method ◽  
Core Shell ◽  
Adsorption Desorption

Core-shell structured hydroxyapatite (HA)/meso-silica was prepared and used as absorbance of methylene blue (MB). HA/meso-silica was synthesized in three steps: preparation of nano-sized HA by wet precipitation method, coating of dense silica and deposition of meso-silica shell on HA. As-received samples were characterized by Fourier transformed infare spectra, small angle X-ray diffraction, nitrogen adsorption-desorption isotherm and transmission electron microscopy. A wormhole framework mesostructure was found for HA/meso-silica. The specific surface area and pore volume were 128 m2•g-1 and 0.36 cm3•g-1, respectively. From the adsorption isotherm, HA/meso-silica with the great specific surface area exhibited a prominent adsorption capacity of MB (134.0 mg/g) in comparison with bare HA (0 mg/g). This study might shed light on surface modification of conventional low-cost adsorbents for removal of organic pollutants from aqueous solutions.

Facile Preparation of Iron-Manganese Oxide@Diatomite Composite for Effective Removal of Vanadium from Wastewater

2019 ◽  
Vol 72 (9) ◽  
pp. 717
Author(s):  
Junying Song ◽  
Zhanbin Huang ◽  
Fengzhi Yang
Keyword(s):  
Specific Surface ◽  
Manganese Oxide ◽  
Surface Area ◽  
Specific Surface Area ◽  
Photoelectron Spectroscopy ◽  
Pore Volume ◽  
Low Cost ◽  
Order Kinetic ◽  
Environmental Friendliness ◽  
Iron Manganese

Excess pentavalent vanadium(v) has severely degraded water quality and posed a huge threat to human health over the past several decades. Hence, it’s urgent and significant to explore a novel adsorbent which is low cost and efficient to treat vanadium pollution. In this work, a novel iron-manganese oxide@diatomite (MnFe2O4@DE) adsorbent with superior removal performance for simulated vanadium(v) wastewater was synthesised via a facile hydrothermal method. The as-prepared MnFe2O4@DE composite was characterised through different characterisation techniques. The results indicated that the MnFe2O4 nanoparticles were uniformly deposited on the surface of diatomite, resulting in a larger specific surface area and pore volume of the composite. In addition, the MnFe2O4@DE adsorbent exhibited the highest adsorption capacity for vanadium(v) (18.37mgg−1±0.5%), which was up to around 13.24 and 1.33 times as much as that of pure diatomite and MnFe2O4, respectively. This is mainly attributed to the enhanced specific surface area and pore volume. Furthermore, X-ray photoelectron spectroscopy (XPS) analysis demonstrated vanadium(v) could be reduced to low valence vanadium with low toxicity by the MnFe2O4@DE composite which could exist as VO2+ and VO+ cations in solution. The adsorption process was better fitted with a pseudo-second-order kinetic model and Langmuir model, which is spontaneous and endothermic. Overall, the novel MnFe2O4@DE composite could be applied as a promising adsorbent in addressing vanadium pollution issues due to its properties of low cost, effectiveness, and environmental friendliness.

Preparation, characterization and catalytic properties of yttrium-zirconium-pillared montmorillonite and their application in supported Ce catalysts

Clay Minerals ◽  
2015 ◽  
Vol 50 (2) ◽  
pp. 211-219 ◽  
Author(s):  
Bo Xue ◽  
Hongmei Guo ◽  
Lujie Liu ◽  
Min Chen
Keyword(s):  
Catalytic Activity ◽  
Ethyl Acetate ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Active Sites ◽  
Industrial Applications ◽  
High Catalytic Activity ◽  
Total Oxidation ◽  
Pillared Montmorillonite

AbstractA new yttrium-zirconium-pillared montmorillonite (Y-Zr-MMT), was synthesized, characterized and used as a Ce catalyst support. The Y-Zr-MMT is a good support for dispersing cerium active sites and it is responsible for the high activity in the total oxidation of acetone, toluene and ethyl acetate. The Y-Zr-MMT shows greater advantages than the conventional alumina/cordierite honeycomb supports such as large specific surface area, lower cost and easier preparation. Catalytic tests demonstrated that Ce/Y-Zr-MMT (Ce loading 8.0%) was the most active, with the total oxidation of acetone, toluene and ethyl acetate being achieved at 220, 300 and 220°C, respectively. The catalyst displayed better activity for the oxidation of acetone and ethyl acetate than a conventional, supported Pd-catalyst under similar conditions. The special structure of the yttrium-doped zirconium-pillared montmorillonite can strengthen the interaction between the CeO2 and Zr-MMT support and improve the dispersion of the Ce particles, which enhances the catalytic activity for the oxidation of VOCs. The new catalyst, 8.0%Ce/Y-Zr-MMT, could be promising for industrial applications due to its high catalytic activity and low cost. The support and the catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET specific surface area measurements.

High-activity oxygen reduction catalyst based on low-cost bagasse, nitrogen and large specific surface area

Energy ◽  
2016 ◽  
Vol 115 ◽  
pp. 397-403 ◽  
Author(s):  
Wenjing Yuan ◽  
Anjian Xie ◽  
Shikuo Li ◽  
Fangzhi Huang ◽  
Peigen Zhang ◽  
...  
Keyword(s):  
Specific Surface ◽  
Oxygen Reduction ◽  
High Activity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Low Cost ◽  
Large Specific Surface Area ◽  
Oxygen Reduction Catalyst

scholarly journals A Type of MOF-Derived Porous Carbon with Low Cost as an Efficient Catalyst for Phenol Hydroxylation

2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Renjie Zhou ◽  
Gui Chen ◽  
Yuejun Ouyang ◽  
Hairui Ni ◽  
Nonglin Zhou ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Porous Carbon ◽  
Physical Adsorption ◽  
Low Cost ◽  
High Specific Surface Area ◽  
Phenol Hydroxylation ◽  
Efficient Catalyst

Using MOF-5 as a template, the porous carbon (MDPC-600) possessing high specific surface area was obtained after carbonization and acid washing. After MDPC-600 was loaded with Cu ions, the catalyst Cu/MDPC-600 was acquired by heat treatment under nitrogen atmosphere. The catalyst was characterized by X-ray powder diffraction (XRD), N2 physical adsorption (BET), field emission electron microscope (SEM), energy spectrum, and transmission electron microscope (TEM). The results show that the Cu/MDPC-600 catalyst prepared by using MOF-5 as the template has a very high specific surface area, and Cu is uniformly supported on the carrier. The catalytic hydrogen peroxide oxidation reaction of phenol hydroxylation was investigated and exhibits better catalytic activity and stability in the phenol hydroxylation reaction. The catalytic effect was best when the reaction temperature was 80°C, the reaction time was 2 h, and the amount of catalyst was 0.05 g. The conversion rate of phenol was 47.6%; the yield and selectivity of catechol were 37.8% and 79.4%, respectively. The activity of the catalyst changes little after three cycles of use.

scholarly journals The Effect of NaOH and KOH on the Characterization of Mesoporous AlOOH Nanostructures in the Hydrothermal Route

2017 ◽  
Vol 58 (2) ◽  
Author(s):  
Nahid Haghnazari ◽  
Mozaffar Abdollahifar ◽  
Farahnaz Jahani
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Hydrothermal Treatment ◽  
Specific Surface Area ◽  
Analytical Techniques ◽  
Aluminium Nitrate ◽  
Hydrothermal Route ◽  
Bet Specific Surface Area ◽  
Adsorption Desorption

Mesoporous AlOOH was synthesized by hydrothermal treatment from aluminium nitrate and NaOH or KOH. The effect of NaOH and KOH as precipitating agents on the characterization of samples were investigated. xrd, ftir, fesem and N<sub>2</sub> adsorption-desorption analytical techniques were used to characterize the products. Our results showed that using KOH as precipitating agent was favourable for the formation of mesoporous and crystalline AlOOH with high bet-specific surface area of 98 m<sup>2</sup>/g.

scholarly journals Adsorptive removal of azithromycin from aqueous solutions using raw and saponin-modified nano diatomite

2019 ◽  
Vol 80 (5) ◽  
pp. 939-949
Author(s):  
Siavash Davoodi ◽  
Behnaz Dahrazma ◽  
Nasser Goudarzi ◽  
Hajar Ghasemian Gorji
Keyword(s):  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Low Cost ◽  
Maximum Adsorption Capacity ◽  
X Ray ◽  
Low Concentrations ◽  
Intra Particle Diffusion ◽  
High Concentrations

Abstract This study aims to investigate the performance and mechanism of raw (R-ND) and saponin-modified nano diatomite (M-ND) in the removal of azithromycin from aqueous solutions. Adsorbent characterization was performed using X-ray fluorescence, Brunauer–Emmett–Teller (BET), scanning electron spectroscopy, dynamic light scattering and energy-dispersive X-ray analyses. It was shown that the specific surface area of R-ND was 119.5 m2/g, 14-fold higher than that for raw diatomite, and for M-ND it was 90.1 m2/g. Various adsorption conditions, i.e. adsorbent dosage, pH, initial concentration and contact time were investigated. According to the results, despite reducing the specific surface area by 25%, modification of nano diatomite by saponin markedly enhanced its performance in the removal of azithromycin. The maximum adsorption capacity of R-ND and M-ND in the removal of azithromycin was 68 and 91.7 mg/g, respectively. Fourier transform infrared spectroscopy results revealed that azithromycin was adsorbed by O-H groups on the diatomite surface. Weber–Morris intra-particle diffusion (IPD) model suggested that while IPD is not the rate-controlling step in high concentrations of azithromycin, it is the only step that controls the rate of adsorption in low concentrations. In comparison to R-ND, M-ND showed a higher efficiency in the removal of azithromycin and, therefore, it can be used as a promising low-cost adsorbent to remove azithromycin from aqueous solutions.

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