scholarly journals Application of Factorial Design In The Optimization of A Procedure For Antimony (Sb) Remediation From Wastewater Employing Mesoporous Array

2021 ◽  
Author(s):  
José Arnaldo Santana Costa ◽  
Vinicius Câmara Costa ◽  
Matheus Lima de Mello ◽  
Caio Marcio Paranhos
Keyword(s):  
Factorial Design ◽  
Low Cost ◽  
High Surface ◽  
Aqueous Media ◽  
High Surface Area ◽  
Total Pore Volume ◽  
Mesoporous Structure ◽  
Spherical Particles ◽  
Easy Access ◽  
Type Iv

Abstract This study describes the sustainable and eco-friendly synthesis of the silica-based mesoporous structure from the use of alternative amorphous silica extracted from rice husk ash (RHA). The mesoporous material was called MCM-48 (RHA) and its application as adsorbent to the antimony (Sb) remediation in wastewater was tested. The adsorbent was prepared by an efficient and sustainable hydrothermal method, which exhibited an amorphous framework with type IV isotherms and type H1 hysteresis, high surface area (820.94 m2 g−1) and total pore volume (0.55 cm3 g−1) with a narrow mesopores distribution, uniform spherical particles, and well-defined architecture. Multivariate optimization using a factorial design (24) was employed in the adsorption tests of Sb. The variables evaluated and the conditions selected were: adsorbent mass (45 mg); adsorption time (60 min); pH (ranged from 2 to 10); and concentration of the Sb standard (8 mol L−1). The adsorbent material proposed in this study proved to be efficient for Sb remediation in aqueous media, mainly because it is a material with easy access, low-cost, and eco-friendly.

Facile Synthesis of Activated Carbon from Swamp Taro Stalk via Single Step ZnCl2 Activation

2016 ◽  
Vol 857 ◽  
pp. 475-479 ◽  
Author(s):  
M.S. Mohammed Yahya ◽  
Jeyashelly Andas ◽  
Ghani Zaidi Ab
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Total Pore Volume ◽  
Structure Type ◽  
Sem Analysis ◽  
Single Step ◽  
Bet Surface Area ◽  
Type Iv

In this work, mesoporous activated carbon with high surface area was synthesized from swamp taro stalk by single step ZnCl2 activation. The synthesized activated carbon was characterized by Na2S2O3 volumetric method, Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscope (SEM) and N2 adsorption-desorption analyses. Under the single step ZnCl2 activation, the registered iodine number, BET surface area, total pore volume and pore diameter were 1087.57 mgg-1, 1242.26 m2g-1, 0.73cm3g-1 and 3.72 nm respectively with yield of 25.34%. SEM analysis evidenced the well-formation of porous structure. Type IV isotherm with H2 loops obtained from N2-sorption studies indicates the ink bottles shape mesoporous network structure. This research proved the successful conversion of plant waste into high grade activated carbon.

scholarly journals Nanoporous zirconia microspheres prepared by salt-assisted spray drying

2020 ◽  
Vol 2 (5) ◽  
Author(s):  
M. Skovgaard ◽  
M. Gudik-Sørensen ◽  
K. Almdal ◽  
A. Ahniyaz
Keyword(s):  
Spray Drying ◽  
Low Cost ◽  
Porous Ceramic ◽  
High Surface ◽  
High Surface Area ◽  
Industrial Applications ◽  
Spherical Particles ◽  
Templating Method ◽  
Wide Range ◽  
Zirconia Powders

Abstract Nanoporous zirconia with high surface area and crystallinity has a wide range of industrial applications, such as in inorganic exchangers for ion exchange columns, catalyst substrates, and packing material for HPLC. Spherical particles of crystalline nanoporous zirconia are highly desired in various industries due to easy handling of the materials in a fluidized bed. Here, spray drying was adopted to produce spherical nanoporous zirconia powders in both laboratory scale and pilot plant scale. Effect of salts on spray-dried ZrO2 powders and their crystallization behavior was studied. It was found that addition of salts to the zirconia precursors has a huge effect on the crystallization of nanoporous zirconia powders. These results have a great impact on the development of microspheres of nanocrystalline ZrO2 and potentially open up a new opportunity to the low-cost production of porous ceramic microspheres with the salt templating method, in general.

scholarly journals Synthesis of catalysts with fine platinum particles supported by high-surface-area activated carbons and optimization of their catalytic activities for polymer electrolyte fuel cells

RSC Advances ◽  
2021 ◽  
Vol 11 (33) ◽  
pp. 20601-20611
Author(s):  
Md. Mijanur Rahman ◽  
Kenta Inaba ◽  
Garavdorj Batnyagt ◽  
Masato Saikawa ◽  
Yoshiki Kato ◽  
...  
Keyword(s):  
Fuel Cells ◽  
Polymer Electrolyte ◽  
High Performance ◽  
Activated Carbons ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Polymer Electrolyte Fuel Cells ◽  
Supported Platinum ◽  
Platinum Particles

Herein, we demonstrated that carbon-supported platinum (Pt/C) is a low-cost and high-performance electrocatalyst for polymer electrolyte fuel cells (PEFCs).

scholarly journals Effects of Annealing Temperature on the Oxygen Evolution Reaction Activity of Copper–Cobalt Oxide Nanosheets

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 657
Author(s):  
Geul Han Kim ◽  
Yoo Sei Park ◽  
Juchan Yang ◽  
Myeong Je Jang ◽  
Jaehoon Jeong ◽  
...  
Keyword(s):  
High Activity ◽  
Cobalt Oxide ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Cobalt Hydroxide ◽  
Ni Foam ◽  
Electron Conduction

Developing high performance, highly stable, and low-cost electrodes for the oxygen evolution reaction (OER) is challenging in water electrolysis technology. However, Ir- and Ru-based OER catalysts with high OER efficiency are difficult to commercialize as precious metal-based catalysts. Therefore, the study of OER catalysts, which are replaced by non-precious metals and have high activity and stability, are necessary. In this study, a copper–cobalt oxide nanosheet (CCO) electrode was synthesized by the electrodeposition of copper–cobalt hydroxide (CCOH) on Ni foam followed by annealing. The CCOH was annealed at various temperatures, and the structure changed to that of CCO at temperatures above 250 °C. In addition, it was observed that the nanosheets agglomerated when annealed at 300 °C. The CCO electrode annealed at 250 °C had a high surface area and efficient electron conduction pathways as a result of the direct growth on the Ni foam. Thus, the prepared CCO electrode exhibited enhanced OER activity (1.6 V at 261 mA/cm2) compared to those of CCOH (1.6 V at 144 mA/cm2), Co3O4 (1.6 V at 39 mA/cm2), and commercial IrO2 (1.6 V at 14 mA/cm2) electrodes. The optimized catalyst also showed high activity and stability under high pH conditions, demonstrating its potential as a low cost, highly efficient OER electrode material.

scholarly journals Glucose/Graphene-Based Aerogels for Gas Adsorption and Electric Double Layer Capacitors

Polymers ◽  
2018 ◽  
Vol 11 (1) ◽  
pp. 40 ◽  
Author(s):  
Kang-Kai Liu ◽  
Biao Jin ◽  
Long-Yue Meng
Keyword(s):  
Gas Adsorption ◽  
High Surface ◽  
Aqueous Media ◽  
High Surface Area ◽  
Three Dimensional ◽  
High Specific Capacitance ◽  
Mesopore Size Distribution ◽  
Excellent Electrochemical Performance ◽  
Double Layer Capacitors ◽  
Hydrothermal Reduction

In this study, three-dimensional glucose/graphene-based aerogels (G/GAs) were synthesized using the hydrothermal reduction and CO2 activation method. Graphene oxide (GO) was used as a matrix, and glucose was used as a binder for the orientation of the GO morphology in an aqueous media. We determined that G/GAs exhibited narrow mesopore size distribution, a high surface area (763 m2 g−1), and hierarchical macroporous and mesoporous structures. These features contributed to G/GAs being promising adsorbents for the removal of CO2 (76.5 mg g−1 at 298 K), CH4 (16.8 mg g−1 at 298 K), and H2 (12.1 mg g−1 at 77 K). G/GAs presented excellent electrochemical performance, featuring a high specific capacitance of 305.5 F g−1 at 1 A g−1, and good cyclic stability of 98.5% retention after 10,000 consecutive charge-discharge cycles at 10 A g−1. This study provided an efficient approach for preparing graphene aerogels exhibiting hierarchical porosity for gas adsorption and supercapacitors.

Morphology dependent adsorption of methylene blue on trititanate nanoplates and nanotubes prepared by the hydrothermal treatment of TiO2

2016 ◽  
Vol 75 (2) ◽  
pp. 350-357
Author(s):  
Graham Dawson ◽  
Wei Chen ◽  
Luhua Lu ◽  
Kai Dai
Keyword(s):  
Methylene Blue ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Pore Volume ◽  
Hydrothermal Reaction ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
High Capacity ◽  
Adsorption Properties

The adsorption properties of two nanomorphologies of trititanate, nanotubes (TiNT) and plates (TiNP), prepared by the hydrothermal reaction of concentrated NaOH with different phases of TiO2, were examined. It was found that the capacity for both morphologies towards methylene blue (MB), an ideal pollutant, was extremely high, with the TiNP having a capacity of 130 mg/g, higher than the TiNT, whose capacity was 120 mg/g at 10 mg/L MB concentration. At capacity, the well-dispersed powders deposit on the floor of the reaction vessel. The two morphologies had very different structural and adsorption properties. TiNT with high surface area and pore volume exhibited exothermic monolayer adsorption of MB. TiNP with low surface area and pore volume yielded a higher adsorption capacity through endothermic multilayer adsorption governed by pore diffusion. TiNP exhibited a higher negative surface charge of −23 mV, compared to −12 mV for TiNT. The adsorption process appears to be an electrostatic interaction, with the cationic dye attracted more strongly to the nanoplates, resulting in a higher adsorption capacity and different adsorption modes. We believe this simple, low cost production of high capacity nanostructured adsorbent material has potential uses in wastewater treatment.

Hard-templating synthesis and enhanced photocatalysis of mesoporous titanium dioxides nanoparticles

2018 ◽  
Vol 11 (04) ◽  
pp. 1850077 ◽  
Author(s):  
K. L. Jin ◽  
X. J. Chen ◽  
J. C. Xu ◽  
Y. S. Huang ◽  
Y. B. Han ◽  
...  
Keyword(s):  
Surface Area ◽  
Anatase Phase ◽  
High Surface ◽  
High Surface Area ◽  
Mesoporous Structure ◽  
Photocatalytic Decomposition ◽  
Titanium Dioxides ◽  
Decomposition Efficiency ◽  
Templating Synthesis ◽  
Mb Adsorption

Mesoporous titanium dioxides nanoparticles (TiO2 NPs) were synthesized using activated carbon (AC) as templates after the decomposition of AC. All results indicated that TiO2 NPs with the small grain size presented the anatase phase structure. Mesoporous TiO2 NPs showed the high surface area and the surface area decreased with the TiO2 content. The removal of methylene blue (MB) indicated that the photocatalytic decomposition efficiency of mesoporous TiO2 NPs increased up to 92% for three-times doping with the TiO2 content, and then decreased. This should be attributed to the synergistic effect from the MB adsorption of mesoporous-structure and the photocatalysis of TiO2 NPs. Therefore, the higher MB concentration near TiO2 NPs from the mesoporous-structure increased the touch chance and the MB photocatalytic decomposition was promoted greatly.

Highly active mixed-valent MnOxspheres constructed by nanocrystals as efficient catalysts for long-cycle Li–O2batteries

2016 ◽  
Vol 4 (43) ◽  
pp. 17129-17137 ◽  
Author(s):  
Sanpei Zhang ◽  
Zhaoyin Wen ◽  
Yang Lu ◽  
Xiangwei Wu ◽  
Jianhua Yang
Keyword(s):  
Surface Area ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Long Cycle ◽  
Highly Active

We demonstrate a low-cost and facile strategy to synthesize mixed-valent MnOxspheres constructed from nanocrystals (~5 nm), containing MnII, MnIII, and MnIVspecies. Such highly active mixed-valent MnOxspheres with high surface area greatly improve the performance of Li–O2batteries.

Influence of nanoparticles on the polymer-conditioned dewatering of wastewater sludges

2013 ◽  
Vol 67 (9) ◽  
pp. 2117-2123
Author(s):  
N. J. Boyle ◽  
G. M. Evans
Keyword(s):  
Activated Sludge ◽  
Titanium Dioxide Nanoparticles ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Wastewater Sludge ◽  
Small Scale ◽  
Sludge Dewatering ◽  
Solids Content ◽  
The Impact

The effect of using small-scale, high surface area, nanoparticles to supplement polymer-conditioned wastewater sludge dewatering was investigated. Aerobically digested sludge and waste activated sludge sourced from the Hunter Valley, NSW, Australia, were tested with titanium dioxide nanoparticles. The sludge samples were dosed with the nanoparticles in an attempt to adsorb a component of the charged biopolymer surfactants present naturally in sludge. The sludge was conditioned with a cationic polymer. The dewatering characteristics were assessed by measuring the specific resistance to filtration through a modified time-to-filter testing apparatus. The solids content of the dosed samples was determined by a mass balance and compared to the original solids content in the activated sludge. Test results indicated that nanoparticle addition modified the structure of the sludge and provided benefits in terms of the dewatering rate. The samples dosed with nanoparticles exhibited faster water removal, indicating a more permeable filter cake and hence more permeable sludge. A concentration of 2–4% nanoparticles was required to achieve a noticeable benefit. As a comparison, the sludge samples were also tested with a larger particle size, powdered activated carbon (PAC). It was found that the PAC did provide some minor benefits to sludge dewatering but was outperformed by the nanoparticles. The solids content of the final sludge was increased by a maximum of up to 0.6%. The impact of the order sequence of particles and polymer was also investigated. It was found that nanoparticles added before polymer addition provided the best dewatering performance. This outcome was consistent with current theories and previous research through the literature. An economic analysis was undertaken to confirm the viability of the technology for implementation at a full-scale plant. It was found that, currently, this technology is unlikely to be favourable unless the nanoparticles can be sourced for a low cost.

scholarly journals Green and facile synthesis of cerium doped Ni3Fe electrocatalyst for efficient oxygen evolution reaction

2020 ◽  
Vol 34 (2) ◽  
pp. 353-363
Author(s):  
F. Kanwal ◽  
A. Batool ◽  
R. Akbar ◽  
S. Asim ◽  
M. Saleem
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Large Scale ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Alkaline Electrolyte ◽  
Hydrogen Electrode ◽  
Molar Ratios

Electrochemical water splitting is the most promising pathway to produce high-purity hydrogen to alleviate global energy crisis. This reaction demands inexpensive, efficient and robust electrocatalyst for its commercial use. Herein, we demonstrate an effective, facile and scalable method for the synthesis of cerium doped Ni3Fe nanostructures as an electrocatalyst for oxygen evolution reaction (OER) by following simple chemical bath deposition route. The different molar ratios (3, 6 and 12 mM) of cerium in the chemical bath were used to study its effect on the structural and the electrochemical properties of the Ni3Fe nanostructured films. Doping of cerium contents induced variations in the morphology of deposited Ni3Fe nanostructures. The optimized electrocatalyst Ni3Fe/Ce-6 yielded high surface area catalyst nanosheets uniformly deposited on three-dimensional conductive scaffold to ensure increase in the exposure of doped Ni3Fe catalytic sites with high electrical conductivity. As a result, this earth-abundant electrocatalyst affords high OER performance with a small overpotential of 310 mV versus reversible hydrogen electrode (RHE) at 10 mA cm-2 and retains good stability up to ~ 10 h in alkaline electrolyte. This scalable strategy has great potential in future advancement of efficient and low-cost electrocatalysts for their large-scale application in energy conversion systems.                     KEY WORDS: Oxygen evolution, Electrocatalyst, Ni3Fe nanostructures, Cerium, Alkaline electrolyte   Bull. Chem. Soc. Ethiop. 2020, 34(2), 353-363 DOI: https://dx.doi.org/10.4314/bcse.v34i2.12

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