scholarly journals Investigation of activated Al-pillared clay efficiency in vegetable oil purification

2004 ◽  
pp. 31-36 ◽  
Author(s):  
Gizela Lomic ◽  
Erne Kis ◽  
Etelka Dimic ◽  
Ranko Romanic
Keyword(s):  
Surface Area ◽  
Vegetable Oil ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Sample Surface ◽  
Pillared Clay ◽  
Acid Activation ◽  
Micropore Surface Area ◽  
Natural Clays ◽  
Oil Purification

This paper represents a contribution to the applicability of natural clays and their derivates as adsorbents in the process of purification of vegetable oil. Investigation of textural properties of raw and purified clay samples reveals that during acid activation and Al-pillaring, BET and micropore surface area increases significantly. However, bleaching capacity of clay and its derivates is not determined by using sample surface area, but rather sample total pore volume. Surface area, especially micropore surface area contributes to removal of smaller molecules. This was confirmed by successful elimination of moisture and volatile materials by samples with an appropriate micropore structure. Used samples of clay and its derivates do not significantly influence acid and peroxide values of raw sunflower oil during its treatment.

scholarly journals On the Gas Storage Properties of 3D Porous Carbons Derived from Hyper-Crosslinked Polymers

Polymers ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 588 ◽  
Author(s):  
Giorgio Gatti ◽  
Mina Errahali ◽  
Lorenzo Tei ◽  
Maurizio Cossi ◽  
Leonardo Marchese
Keyword(s):  
Thermal Treatment ◽  
Surface Area ◽  
Pore Volume ◽  
Chemical Activation ◽  
Chemical Characterization ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Gas Storage ◽  
Bet Surface Area ◽  
Porous Carbons

The preparation of porous carbons by post-synthesis treatment of hypercrosslinked polymers is described, with a careful physico-chemical characterization, to obtain new materials for gas storage and separation. Different procedures, based on chemical and thermal activations, are considered; they include thermal treatment at 380 °C, and chemical activation with KOH followed by thermal treatment at 750 or 800 °C; the resulting materials are carefully characterized in their structural and textural properties. The thermal treatment at temperature below decomposition (380 °C) maintains the polymer structure, removing the side-products of the polymerization entrapped in the pores and improving the textural properties. On the other hand, the carbonization leads to a different material, enhancing both surface area and total pore volume—the textural properties of the final porous carbons are affected by the activation procedure and by the starting polymer. Different chemical activation methods and temperatures lead to different carbons with BET surface area ranging between 2318 and 2975 m2/g and pore volume up to 1.30 cc/g. The wise choice of the carbonization treatment allows the final textural properties to be finely tuned by increasing either the narrow pore fraction or the micro- and mesoporous volume. High pressure gas adsorption measurements of methane, hydrogen, and carbon dioxide of the most promising material are investigated, and the storage capacity for methane is measured and discussed.

The Influence of Acid Treatment on the Nanostructure and Textural Properties of Bentonite Clays

2005 ◽  
Vol 494 ◽  
pp. 339-344 ◽  
Author(s):  
Z. Vuković ◽  
A. Milutinović-Nikolić ◽  
J. Krstić ◽  
A. Abu-Rabi ◽  
T. Novaković ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Acid Concentration ◽  
Pore Volume ◽  
Acid Treatment ◽  
Textural Properties ◽  
Nitrogen Adsorption ◽  
Acid Activation ◽  
Bentonite Clays

The nanostructure and textural properties of acid-activated bentonite clays from the Bogovina coalmine were investigated. The acid activation was performed with HCl in the concentration range 1.5-7.5 M. The atomic force microscopy followed by image analysis was used in order to establish the influence of the acid treatment on the size of bentonite particles. Nitrogen adsorption-desorption isotherms at -196 °C were used to estimate the specific surface area, pore volume and pore size distribution. The acid treatment reduces the size of bentonite particles and increases the specific surface area and pore volume of the investigated bentonites. These effects are improved by increasing the acid concentration up to 4.5 M HCl. Further increase in acid concentration does not result in development of new porous structure.

Chemical Activation of Durian Shell Activated Carbon: Effects of Activation Agents

2015 ◽  
Vol 1113 ◽  
pp. 242-247
Author(s):  
Wan Norasiah Wan Mahmood ◽  
Rusnah Samsuddin ◽  
Raja Razuan Raja Deris
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Potassium Hydroxide ◽  
Chemical Activation ◽  
High Surface ◽  
High Surface Area ◽  
Total Pore Volume ◽  
Surface Porosity ◽  
Micropore Surface Area ◽  
Selection Of

Selection of suitable activation agent is important in order to produce high surface area of activated carbon. The present study was undertaken to develop high surface area of durian shell activated carbon (DSAC) using different chemical activation agents which were potassium hydroxide (KOH) and phosphoric acid (H3PO4). Surface porosity and surface area were directly measured from scanning electron microscopy (SEM) and surface area analyzer, respectively. For the optimum condition, it showed that H3PO4 treated DSAC had the highest surface area which was 257.50 m2/g compared to KOH treated DSAC which was 13.10 m2/g. H3PO4 treated DSAC also showed the highest micropore surface area, external surface area and total pore volume with 191.22 m2/g, 66.28 m2/g and 0.149 cm3/g, respectively. SEM result showed that H3PO4 treated DSAC had a well pronounce porosity than durian shell char. Surface area and surface porosity were important in an adsorption process.

scholarly journals Comparison of the Surface Properties of Hydrothermally Synthesised Fe3O4@C Nanocomposites at Variable Reaction Times

Nanomaterials ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 2742
Author(s):  
Sadiq Sani ◽  
Rohana Adnan ◽  
Wen-Da Oh ◽  
Anwar Iqbal
Keyword(s):  
Surface Area ◽  
Pore Volume ◽  
Pore Diameter ◽  
Hydrothermal Process ◽  
Reaction Times ◽  
Total Pore Volume ◽  
Textural Properties ◽  
P Value ◽  
Electron Microscopies ◽  
Crystallite Sizes

The influence of variable reaction time (tr) on surface/textural properties (surface area, total pore volume, and pore diameter) of carbon-encapsulated magnetite (Fe3O4@C) nanocomposites fabricated by a hydrothermal process at 190 °C for 3, 4, and 5 h was studied. The properties were calculated using the Brunauer–Emmett–Teller (BET) isotherms data. The nanocomposites were characterised using Fourier transform infrared spectroscopy, X-ray diffraction analysis, thermogravimetry, and scanning and transmission electron microscopies. Analysis of variance shows tr has the largest effect on pore volume (F value = 1117.6, p value < 0.0001), followed by the surface area (F value = 54.8, p value < 0.0001) and pore diameter (F value = 10.4, p value < 0.001) with R2-adjusted values of 99.5%, 88.5% and 63.1%, respectively. Tukey and Fisher tests confirmed tr rise to have caused increased variations in mean particle sizes (11–91 nm), crystallite sizes (5–21 nm), pore diameters (9–16 nm), pore volume (0.017–0.089 cm3 g−1) and surface area (7.6–22.4 m2 g−1) of the nanocomposites with individual and simultaneous confidence limits of 97.9 and 84.4 (p-adj < 0.05). The nanocomposites’ retained Fe–O vibrations at octahedral (436 cm−1) and tetrahedral (570 cm−1) cubic ferrite sites, modest thermal stability (37–60% weight loss), and large volume-specific surface area with potential for catalytic application in advanced oxidation processes.

scholarly journals Nanometer Pore Structure Characterization of Taiyuan Formation Shale in the Lin-Xing Area Based on Nitrogen Adsorption Experiments

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 298
Author(s):  
Chenlong Ding ◽  
Jinxian He ◽  
Hongchen Wu ◽  
Xiaoli Zhang
Keyword(s):  
Specific Surface ◽  
Pore Structure ◽  
Surface Area ◽  
Specific Surface Area ◽  
Shale Gas ◽  
Pore Volume ◽  
Ordos Basin ◽  
Total Pore Volume ◽  
Nitrogen Adsorption ◽  
Taiyuan Formation

Ordos Basin is an important continental shale gas exploration site in China. The micropore structure of the shale reservoir is of great importance for shale gas evaluation. The Taiyuan Formation of the lower Permian is the main exploration interval for this area. To examine the nanometer pore structures in the Taiyuan Formation shale reservoirs in the Lin-Xing area, Northern Shaanxi, the microscopic pore structure characteristics were analyzed via nitrogen adsorption experiments. The pore structure parameters, such as specific surface area, pore volume, and aperture distribution, of shale were calculated; the significance of the pore structure for shale gas storage was analyzed; and the main controlling factors of pore development were assessed. The results indicated the surface area and hole volume of the shale sample to be 0.141–2.188 m2/g and 0.001398–0.008718 cm3/g, respectively. According to the IUPAC (International Union of Pure and Applied Chemistry) classification, mesopores and macropores were dominant in the pore structure, with the presence of a certain number of micropores. The adsorption curves were similar to the standard IV (a)-type isotherm line, and the hysteresis loop type was mainly similar to H3 and H4 types, indicating that most pores are dominated by open type pores, such as parallel plate-shaped pores and wedge-shaped slit pores. The micropores and mesopores provide the vast majority of the specific surface area, functioning as the main area for the adsorption of gas in the shale. The mesopores and macropores provide the vast majority of the pore volume, functioning as the main storage areas for the gas in the shale. Total organic carbon had no notable linear correlation with the total pore volume and the specific surface area. Vitrinite reflectance (Ro) had no notable correlation with the specific surface area, but did have a low “U” curve correlation with the total pore volume. There was no relationship between the quartz content and specific surface area and total pore volume. In addition, there was no notable correlation between the clay mineral content and total specific surface area and total pore volume.

scholarly journals Characterization and Catalytic Behaviour of Co3(PO4)2–AlPO4 Catalysts

1998 ◽  
Vol 16 (4) ◽  
pp. 285-293 ◽  
Author(s):  
M.R. Mostafa ◽  
F.Sh. Ahmed
Keyword(s):  
Pore Radius ◽  
Surface Acidity ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Acid Sites ◽  
Adsorption Of Nitrogen ◽  
Amorphous Structures ◽  
Ft Ir ◽  
Catalytic Behaviour ◽  
The Mean

Co3(PO4)2, AlPO4 and the binary system Co3(PO4)2-AlPO4 with different compositions were prepared by the coprecipitation method. The structural properties of these samples were determined using XRD, DTA and FT-IR techniques. The textural properties were determined from the adsorption of nitrogen at 77 K. The surface acidity was measured by a calorimetric titration method. The samples were tested as catalysts in the dehydration of ethanol and isopropanol using a pulse microcatalytic technique. The data obtained from XRD and FT-IR indicate the amorphous structures of the prepared catalysts. An increase in Co3(PO4)2 content led to a decrease in the surface area and in the total pore volume and an increase in the mean pore radius. The surface acidity of the catalyst depends on the chemical composition; the surface acidity increased with an increase in the AlPO4 content. The dehydration temperature and the distribution of acid sites are important parameters in determining the selectivity and activity of the catalyst.

Characterization and catalytic properties of a saponite clay modified by acid activation

Clay Minerals ◽  
1997 ◽  
Vol 32 (4) ◽  
pp. 633-643 ◽  
Author(s):  
F. Kooli ◽  
W. Jones
Keyword(s):  
Infrared Spectroscopy ◽  
Room Temperature ◽  
Textural Properties ◽  
Acid Sites ◽  
Single Type ◽  
Activation Process ◽  
Acid Activation ◽  
Strongly Correlated ◽  
Lewis Site ◽  
Adsorbed Pyridine

AbstractA natural saponite was acid activated at room temperature or 90°C with different acid/clay ratios and the products were characterized by powder X-ray diffraction, infrared spectroscopy and thermogravimetry. The leaching of Mg from the octahedral sheets is enhanced by an increase in the acid/clay ratio and by an increase in temperature of activation. Textural properties are reported, and it appears that they are strongly correlated to the presence of a noncrystalline silica phase which is formed during the acid activation process. The desorption of cyclohexylamine indicates that for samples activated at 90°C the number of acid sites in the acidactivated saponites decreases following severe acid treatment. Infrared spectroscopy of adsorbed pyridine on samples after calcination at 500°C suggests that acid activation at 90°C produces a single type of Bronsted site but two types of Lewis sites whereas activation at room temperature results in only one type of Lewis site in addition to a Brønsted site. The two Lewis sites are suggested to originate from residual Al in the clay structure and to AI exsolved from the layers during activation. The dehydration of pentan-1-ol has been used as a further probe to measure acidity by monitoring the degree of conversion and selectivity for the different samples.

scholarly journals Effect of Structure and Chemical Activation on the Adsorption Properties of Green Clay Minerals for the Removal of Cationic Dye

2018 ◽  
Vol 8 (11) ◽  
pp. 2302 ◽  
Author(s):  
Abdelfattah Amari ◽  
Hatem Gannouni ◽  
Mohammad Khan ◽  
Mohammed Almesfer ◽  
Abubakr Elkhaleefa ◽  
...  
Keyword(s):  
Clay Minerals ◽  
Pore Volume ◽  
Acid Treatment ◽  
Structural Changes ◽  
Chemical Activation ◽  
Total Pore Volume ◽  
Batch Adsorption ◽  
Acid Activation ◽  
Cationic Dye ◽  
Average Pore

In this study, natural clay minerals with green appearance were treated with sulfuric acid. Mass percentage of acid (wt%), temperature (T), contact time (t) and liquid-to-solid mass ratio (R) are used as the prevailing factors that determine the extent of acid-activation. The values of these factors range from 15–50%, 60–90 °C, 1.5–6 h and 4–7, respectively. The study has focused on the structural changes as well as textural characteristics of the clay. Three activated clay samples were prepared under different treatment conditions. The samples were characterized using X-ray powder diffraction (XRD), fourier transform infrared (FTIR), scanning electron microscope (SEM), chemical analysis and N2 adsorption techniques. Characterization of the treated clay minerals exhibited significant structural changes to a greater extent of acid-activation, from being partially crystalline to being amorphous silica. The surface area and total pore volume of clay increased proportionally with the level of acid treatment. The average pore diameter behaved differently. During the strong acid treatment, a large increase in pore volume and the enlargement of the pore size distribution were observed. This suggests that considerable structural changes and partial destruction may have occurred in this condition. The removal of methylene blue, used as cationic dye, from aqueous solution by the batch adsorption technique on three prepared acid-activated clay samples was studied. The Langmuir model was found to agree well with the experimental data.

scholarly journals An Eco-Friendly Process for Removal of Lead from Aqueous Solution

2017 ◽  
Vol 11 (5) ◽  
pp. 47 ◽  
Author(s):  
Heman A. Smail ◽  
Kafia M. Shareef ◽  
Zainab H. Ramli
Keyword(s):  
Heavy Metal ◽  
Oxalic Acid ◽  
Surface Area ◽  
Pore Volume ◽  
Metal Ion ◽  
Adsorption Equilibrium ◽  
Total Pore Volume ◽  
Heavy Metal Ion ◽  
Bet Surface Area ◽  
Barley Husk

The adsorption of lead (Pb II) ion on different types of synthesized zeolite was investigated. The BET surface area, total pore volume & average pore size distribution of these synthesized zeolites were determined by adsorption isotherms for N2, the surface area & total pore volume of their sources were found by adsorption isothermN2.The adsorption equilibrium was measured after 24h at room temperature (RT) & concentration 10mg.L-1 of Pb (II) was used. The adsorption of heavy metal Pb (II) on four different prepared zeolites (LTA from Montmorillonite clay, FAU(Y)-B.H (G2) from Barley husk, Mordenite (G1) from Chert rock, FAU(X)-S.C (G3) from shale clay & modified Shale clay by oxalic acid (N1) & sodium hydroxide (N2)), were compared with the adsorption of their sources by using static batch experimental method. The major factors affecting the heavy metal ion sorption on different synthesized zeolites & their sources were investigated. The adsorption equilibrium capacity (Qm) of Pb (II) ion for different synthesized zeolites ordered from (N1>N2>LTA>G3>G2>G1&for their sources ordered Shale clay >Montmorilonite> Barley husk>Chert rock. The atomic absorption spectrometry was used for analysis of lead heavy metal ion, the obtained results in this study showed that the different synthesized zeolites were efficient ion exchanges for removing heavy metal, in particular, the modified zeolite from shale clay by oxalic acid.

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