scholarly journals Adsorption of phosphate ions from an aqueous solution by calcined nickel-cobalt binary hydroxide

2016 ◽  
Vol 75 (1) ◽  
pp. 94-105 ◽  
Author(s):  
Fumihiko Ogata ◽  
Erimi Ueta ◽  
Megumu Toda ◽  
Masashi Otani ◽  
Naohito Kawasaki
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Correlation Coefficients ◽  
Hydroxyl Groups ◽  
Order Model ◽  
Molar Ratios ◽  
Phosphate Ions ◽  
Increasing Temperature ◽  
Adsorption Desorption

Different molar ratios of a Ni/Co binary hydroxide (NiCo82, NiCo91, and Ni100) were prepared and calcined at 270 °C (NiCo82-270, NiCo91-270, and Ni100-270). The properties of the adsorbents and the amount of adsorbed phosphate ions were evaluated. The adsorbents calcined at 270 °C had a nickel oxide structure. The amount of adsorbed phosphate ions, the amount of hydroxyl groups, and the specific surface area of the calcined adsorbents at 270 °C were greater than those of the uncalcined adsorbents. The amount of adsorbed phosphate ions was related to the amount of hydroxyl groups and the specific surface area; the correlation coefficients were 0.966 and 0.953, respectively. The adsorption isotherm data for NiCo91 and NiCo91-270 were fit to both the Freundlich and Langmuir equations. The amount of adsorbed phosphate ions increased with increasing temperature. The experimental data fit the pseudo-second-order model better than the pseudo-first-order model. A neutral pH was optimal for phosphate ion adsorption. In addition, the phosphate ions that were adsorbed onto NiCo91-270 could be recovered using sodium hydroxide, and the adsorbent was useful for the repetitive adsorption/desorption of phosphate ions. Collectively, these results suggest that NiCo91-270 is prospectively useful for the adsorption of phosphate ions from aqueous solutions.

The relationship between geotechnical index properties and the pore-size distribution of compacted clayey silts

2015 ◽  
Vol 22 (6) ◽  
Author(s):  
Nazile Ural
Keyword(s):  
Specific Surface ◽  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Correlation Coefficients ◽  
Liquid Limit ◽  
Index Properties

AbstractIn this study, the relationships between geotechnical index properties and the pore-size distribution of compacted natural silt and artificial soil mixtures, namely, silt with two different clays and three different clay percentages (10%, 20%, and 40%), were examined and compared. Atterberg’s limit tests, standard compaction tests, mercury intrusion porosimetry, X-ray diffraction, scanning electron microscopy (SEM) analysis, and Brunauer-Emmett-Teller specific surface analysis were conducted. The results show that the liquid limit, the cumulative pore volume, and specific surface area of artificially mixed soils increase with an increase in the percentage of clay. The cumulative pore volume and specific surface area with geotechnical index properties were compared. High correlation coefficients were observed between the specific areas and both the liquid limit and the plasticity index, as well as between the cumulative pore volume and both the clay percentage and the

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.

Synthesis of High Quality Porous Carbon from Water Hyacinth

2020 ◽  
Vol 860 ◽  
pp. 173-177
Author(s):  
Otong Nurhilal ◽  
Renaldy Sharin Lesmana ◽  
Karina Ramadayanti ◽  
Sholihatul Habibah ◽  
Sahrul Hidayat ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Porous Carbon ◽  
Water Hyacinth ◽  
Invasive Plant ◽  
Proximate Analysis ◽  
High Quality ◽  
Porous Volume ◽  
Adsorption Desorption

Water Hyacinth (WH) is a plant that can absorb various pollutants in water. However, this plant is categorized as an invasive plant that can become a weed in the waters. To improve the functionality of WH, processing of WH is needed to be used for various applications. One of modifications of WH is as porous carbon for battery cathode composite. In this paper, we reported a synthesis of a porous carbon from WH. WH is processed into carbon by carbonization at various temperatures of 400, 500 and 600 °C with various activators of KOH, H3PO4 and ZnCl2 to obtain high quality porous carbon which has high electrical conductivity, large specific surface area and large porous volume. All synthesized carbons were characterized by proximate analysis measurements, scanning electron microscopy (SEM), and N2 adsorption-desorption measurements. The highest carbon fixed content of 37.79% is obtained from charcoal with a carbonization temperature of 400 °C. The largest specific surface area of 264.77 m2/g was obtained from activated carbon with H3PO4 as activator. The values of pore volume and pore radius were 0.186 cm3/g and 1.56 nm, respectively.

Effect of Synthesis Temperature and Ca/P Ratios on Specific Surface Area of Amorphous Calcium Phosphate

2016 ◽  
Vol 721 ◽  
pp. 172-176 ◽  
Author(s):  
Jana Vecstaudza ◽  
Janis Locs
Keyword(s):  
Calcium Phosphate ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Amorphous Calcium Phosphate ◽  
Calcium Phosphates ◽  
Synthesis Temperature ◽  
Molar Ratios ◽  
Different Temperatures ◽  
Low Crystalline

Amorphous and low crystalline calcium phosphates are prospective candidates for bone implant manufacturing. Amorphous calcium phosphate (ACP) preparation technologies could be improved in terms of specific surface area (SSA) of obtained products. Current study is dedicated to the effect of synthesis temperature and Ca and P molar ratios (Ca/P) on SSA of ACP. Higher SSA can improve bioactivity of biomaterials. ACP was characterized by XRD, FT-IR, SEM and BET N2 adsorption techniques. Spherical nanoparticles (<45 nm in size) were obtained independently of initial Ca/P ratio and synthesis temperature. For the first time comparison of SSA was shown for ACP obtained at different temperatures (0 °C and 20 °C) and Ca/P molar ratios (1.5, 1.67 and 2.2).

Effects of Carbonation on the Specific Surface BET of Cement Mortar Measured by Two Different Methods: Nitrogen Adsorption and Water Adsorption

2014 ◽  
Vol 931-932 ◽  
pp. 421-425 ◽  
Author(s):  
Son Tung Pham ◽  
William Prince
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Water Adsorption ◽  
Cement Mortar ◽  
Nitrogen Adsorption ◽  
Accelerated Carbonation ◽  
Molecular Sizes ◽  
The Difference ◽  
Adsorption Desorption

The objective of this work was to examine the microstructural changes caused by the carbonation of normal mortar. Samples were prepared and subjected to accelerated carbonation at 20°C, 65% relative humidity and 20% CO2concentration. The evolutions of the pore size distribution and the specific surface area during carbonation were calculated from the adsorption - desorption isotherms of water vapour and nitrogen. Conflicts observed in the results showed that the porous domains explored by these two methods are not the same due to the difference in molecular sizes of nitrogen and water. These two techniques therefore help to complementarily evaluate the effects of carbonation. The study also helped to explain why results in the literature diverge greatly on the influence of carbonation on specific surface area.

Effect of pH, Molar Ratio of Fuel to Nitrates and Calcination Temperature on the Glycine-Nitrate Synthesis of Nano CoAl2O4

2010 ◽  
Vol 68 ◽  
pp. 176-181 ◽  
Author(s):  
Seyyed Hamid Jazayeri ◽  
Federica Bondioli ◽  
Shiva Salem ◽  
Ali Allahverdi ◽  
Mansoor Shirvani ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Calcination Temperature ◽  
Specific Surface Area ◽  
Precursor Solution ◽  
Molar Ratio ◽  
Effect Of Ph ◽  
Molar Ratios ◽  
Metal Nitrates ◽  
Powder Characteristics

In this research, solution-based combustion synthesis is applied to prepare the spinel CoAl2O4 pigment from precursor solution of Al(NO3)3 .9H2O, Co(NO3)2 .6H2O and glycine. Effect of pH values (2.5, 7, 10.5), molar ratio of fuel to metal nitrates in the precursor solutions (1.5, 2) and subsequent calcination temperature (800, 1000, 1200 °C) on the powder characteristics are described. Gel formation, morphologies, specific surface area and colour of the powder are characterized using DTA/TG, XRD, TEM, BET and UV-Vis. The results indicate that the crystalline spinel CoAl2O4 is formed at all different Gl/(metal nitrates) molar ratios, pH and temperatures and higher temperature promote the increase of the crystallite size. According to TEM figures most of the particles calcined at 800 and 1000 °C has sizes less than 50 and 100 nm, respectively. Corresponding to results of BET experiment, specific surface area has its maximum values at pH 7 and decreases with increasing of temperature. Finally, colorability test indicates the complete stability of the synthesized powder in the glass matrix.

Mathematical Modeling of Biodiesel Production under Intense Agitation

2016 ◽  
Vol 14 (1) ◽  
pp. 445-451
Author(s):  
Aliakbar Roosta ◽  
Jafar Javanmardi ◽  
Elham Sadat Behineh
Keyword(s):  
Mass Transfer ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Rapeseed Oil ◽  
Catalyst Concentration ◽  
Biodiesel Production ◽  
Transfer Coefficients ◽  
Increasing Temperature ◽  
Intense Agitation

AbstractIn this study, a new approach is proposed to investigate the kinetics of sunflower oil and rapeseed oil transesterification in the presence of potassium hydroxide. Transesterification is a heterogeneous process which affected by a number of parameters, that are not readily available in the literature, such as mass transfer coefficients, partition coefficients, and specific surface area of the dispersed phase. However, under intense agitation condition, mass transfer restrictions may be neglected, and the two phases are supposed to remain in thermodynamic equilibrium, during the process. Therefore, a model was developed independent of the mass transfer coefficient and specific surface area, which is reliable for the intense agitation condition. According to the results, the model is valid at least for mixing rates over 500 rpm. The results of the model were used to study the effects of temperature, methanol-to-oil ratio, and catalyst concentration on the biodiesel conversion. Biodiesel production rate increases with increasing temperature, although rapeseed oil transesterification is more temperature dependent. The results show that the maximum amount of catalyst concentration is less than 1% (by weight); however, the optimum value depends on the operating temperature. The optimum value of the methanol-to-oil-ratio decreases with increasing temperature. Thus, at higher temperatures, less amount of methanol and catalyst are required, which leads to easier purification of biodiesel.

Novel Al2O3–SiO2composite aerogels with high specific surface area at elevated temperatures with different alumina/silica molar ratios prepared by a non-alkoxide sol–gel method

RSC Advances ◽  
2016 ◽  
Vol 6 (7) ◽  
pp. 5611-5620 ◽  
Author(s):  
Xiaodong Wu ◽  
Gaofeng Shao ◽  
Xiaodong Shen ◽  
Sheng Cui ◽  
Ling Wang
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Elevated Temperatures ◽  
Inorganic Salt ◽  
Sol Gel ◽  
High Specific Surface Area ◽  
Gel Method ◽  
Molar Ratios ◽  
Composite Aerogels

We have developed a new sol–gel route to synthesise Al2O3–SiO2composite aerogels with different alumina/silica (Al/Si) molar ratios using an inexpensive inorganic salt.

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.

Sol-gel Synthesis of a Novel χSm2Ti2O7/HZSM-5 Composite Photocatalyst for the Promoted Activity on RBR X-3B Degradation

2017 ◽  
Vol 14 (1) ◽  
pp. 17-25
Author(s):  
Wenjie Zhang ◽  
Jiao Yang ◽  
Ling Du
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Pyrochlore Phase ◽  
Bandgap Energy ◽  
Powder Materials ◽  
Sol Gel Synthesis ◽  
Adsorption Desorption

Background: Pyrochloro structured Sm2Ti2O7 has photocatalytic activity on degradation of organic substances and on hydrogen evolution from water. Powder materials usually encounter the obstacle of separating from treated water. HZSM-5 zeolite is a kind of porous structured material with large surface area. Its role as a support for Sm2Ti2O7 is interesting. Methods: The supported Sm2Ti2O7 was synthesized using sol-gel method. The composite χSm2Ti2O7/HZSM-5 was characterized by XRD, SEM, TEM, FT-IR/FIR, UV-Vis DRS, N2 adsorption- desorption and XPS measurements. Photocatalytic degradation of Reactive Brilliant Red X-3B (RBR X-3B) was measured to evaluate the activity of the composite. Results: Sm2Ti2O7 is in the pyrochlore phase after loading on the surface of HZSM-5 zeolite. The crystal cell of pyrochlore Sm2Ti2O7 continuously expanses with decreasing Sm2Ti2O7 loading content in the composite. Bandgap energy of Sm2Ti2O7 is enlarged after supporting. The specific surface area of Sm2Ti2O7 was enlarged from 9.8 m2/g to 93 m2/g after loading. Both of the adsorption capacity and photocatalytic activity of the χSm2Ti2O7/HZSM-5 are greater than those of pure Sm2Ti2O7. After 120 min of irradiation, 73.1% of the initial RBR X-3B molecules are decomposed on 70%Sm2Ti2O7/HZSM-5, and only 27.7% of the dye is decomposed on the bare Sm2Ti2O7. Conclusion: Sm2Ti2O7 crystal growth is constrained after loading due to dispersion of Sm2Ti2O7 on the surface of HZSM-5. The specific surface area of Sm2Ti2O7 is significantly enlarged after loading. All the supported samples have greatly enhanced photocatalytic activity as compared to the bare Sm2Ti2O7.

Sign in / Sign up

Export Citation Format

Share Document