scholarly journals Physicochemical characterization of three natural clays used as adsorbent for the humic acid removal from aqueous solution

2018 ◽  
Vol 37 (1-2) ◽  
pp. 77-94 ◽  
Author(s):  
Soumahoro Gueu ◽  
Gisèle Finqueneisel ◽  
Thierry Zimny ◽  
Danièle Bartier ◽  
Benjamin Kouassi Yao
Keyword(s):  
Humic Acid ◽  
Adsorption Capacity ◽  
Ligand Exchange ◽  
Electrostatic Interactions ◽  
Hydrophobic Interactions ◽  
Physicochemical Characterization ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
Natural Clays

Adsorption behaviours of humic acid on three natural clays from Ivory Coast were studied. In order to investigate the adsorption mechanism, characterization of clays and the humic acid–clay complex was conducted by using various analytical methods (attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), X-ray diffraction (XRD), specific surface area analysis (BET) and chemical composition). As a result, adsorption process showed that the maximum adsorption capacity of humic acid was achieved at pH = 3 and was found to be to 115 mg/g obtained for the best sample. For all clays, the adsorption was found to be strongly dependent on pH and well fitted by the Langmuir model. In addition, it was shown that the adsorption capacity was linked to the kaolinite content of each sample. The results showed that humic acid adsorption onto clay was made via electrostatic interactions, ligand exchange and hydrophobic interactions. This study showed that clays are valuable adsorbents for the removal of humic acid.

scholarly journals Physicochemical Characterization of Moroccan Natural Clays and the Study of their Adsorption Capacity for the Methyl Orange and Methylene

2020 ◽  
Vol 8 (4) ◽  
pp. 1258-1267
Keyword(s):  
Methyl Orange ◽  
Physicochemical Characterization ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Calcined Clay ◽  
X Ray ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Natural Clays

The objective of this work was the physicochemical characterization of a Moroccan natural clay from the Jorf Arfoud region (Lampert Coodinates: x = 595610, y = 101578) and its valorization in the elimination of organic pollutants (methyl orange MO and methylene blue MB) from aqueous solutions, with the adsorption technique on raw and calcined clay at 500°C. The clay was characterized by chemical analysis such as X-ray fluorescence (XRF), X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron microscopy (SEM). Crude and purified clays, consisting essentially of silica and alumina, are a characteristic property of phyllosilicates and also contain amounts of quartz, kaolinite and calcite as associated minerals. The experiments were performed after optimization of the parameters influencing the system, such as pH, adsorbent mass, initial dye concentration and temperature. The clays used absorb better the MB than MO, for an initial concentration of 10 mg/L and 20 mg/L respectively. Langmuir and Freundlich models of adsorption isotherms were applied to fit experimental equilibrium data. Results have showed that the adsorption of MB and MO followed very well the second order kinetic model on raw clay. The adsorption process was found to be exothermic in the case of MB. However, the adsorption of MO was endothermic.

Adsorption Characteristic of U(VI) on Fe-Immobilized Bentonite

2013 ◽  
Vol 639-640 ◽  
pp. 1300-1306
Author(s):  
Zhen Ping Tang ◽  
Hui Ling ◽  
Shui Bo Xie ◽  
S.Y. Li ◽  
J.S. Wang ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Adsorption Mechanism ◽  
Ph Value ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
Adsorption Characteristic ◽  
Order Kinetic Equation

Fe-immobilized bentonite, prepared with bentonite and FeCl3 was used for the adsorption of uranium(VI) in this study, solution pH, ion strength, contact time and temperature were investigated, structural characterization of Fe-immobilized bentonite was assayed by X-ray Diffraction and Fourier Transform Infrared Spectroscopy. Results indicated that the adsorption capacity were strongly affected by the solution pH and ion strength, the adsorption efficiency was 91.8% when pH value was 6 and ion strength was 0.01 mol•L-1, higher or lower pH did not favor the U(VI) adsorption. The adsorption mechanism was discussed by the views of reactive kinetics and thermodynamics along with Scanning Electron Microscope. The adsorption kinetics process was fitted well with the second-order kinetic equation, when the initial U(VI) concentration was less than 38.08mg/L, Langmuir equations could describe the adsorption isotherm of U(VI) well with the maximum adsorption capacity of 169.5mg/g at 303K

Tamanrasset’s Clay Characterization and Use as Low Cost, Ecofriendly and Sustainable Material for Water Treatment: Progress and Challenge in Copper Cu (II)

2021 ◽  
Vol 406 ◽  
pp. 457-472
Author(s):  
Aicha Kourim ◽  
Moulay Abderrahmane Malouki ◽  
Aicha Ziouche ◽  
Mouna Boulahbal ◽  
Madjda Mokhtari
Keyword(s):  
Adsorption Capacity ◽  
Metal Ion ◽  
Low Cost ◽  
Ion Concentration ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pseudo Second Order ◽  
Equilibrium Process

In this study, the adsorption of copper Cu (II) from aqueous solution, on Tamanrasset’s clay which is low cost adsorbent, was studied using batch experiments. The adsorption study includes both equilibrium adsorption isotherms and kinetics. The characterization of the adsorbent necessitated several methods such as X-Ray Diffraction, Scanning Electron Microscopy coupled with Energy Dispersive X-ray, BET for specific surface area determination, Fourier transform infrared spectroscopy and thermogravimetric analysis. Indeed, various parameters were investigated such as contact time, initial metal ion concentration, mass of solid, pH of the solution and temperature. The adsorption process as batch study was investigated under the previews experimental parameters. The results revealed that the adsorption capacity of Cu2+ is maximized at naturel pH of metal 5.5. Removal of copper by the clay of Tamanrasset (kaolinite) achieved equilibrium within 50 minutes; the results obtained were found to be fitted by the pseudo-second order kinetics model. The equilibrium process was well described by the Langmuir model and the maximum adsorption capacity was found to be 26.59 mg/g.

scholarly journals Fabrication, characterization, and adsorption capacity of Fe3O4/graphene oxide nanocomposites for nickel removal

2016 ◽  
Vol 19 (3) ◽  
pp. 60-68
Author(s):  
Hieu Huu Nguyen ◽  
Nam Minh Hoang ◽  
Diem Thi Hoai Phan
Keyword(s):  
Graphene Oxide ◽  
Adsorption Capacity ◽  
Ph Effect ◽  
Maximum Adsorption Capacity ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Langmuir Isotherm Model ◽  
Modified Hummers Method

In this research, graphene oxide (GO) was synthesized via modified Hummers’ method and for the preparation of Fe3O4/GO nanocomposites by impregnation method. Characterization of the nanocomposites was performed by X–ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscope, specific surface area, and vibrating sample magnetometer. The concentration of Ni (II) ion in solutions was determined using UV-Visible spectrophoto-meter. The adsorption capacity for Ni (II) removal was examined with respect to pH effect, kinetic data and equilibrium isotherms in batch experiments. The maximum adsorption capacity of the Fe3O4/GO estimated with the Langmuir-isotherm model for Ni (II) was 27.62 mg/g at room temperature.

scholarly journals Removal of humic acid from aqueous solution using polyacrylamide/chitosan semi-IPN hydrogel

2018 ◽  
Vol 2017 (1) ◽  
pp. 16-26 ◽  
Author(s):  
Zejun Liu ◽  
Shaoqi Zhou
Keyword(s):  
Aqueous Solution ◽  
Humic Acid ◽  
Ionic Strength ◽  
Adsorption Capacity ◽  
Electrostatic Interactions ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Initial Ph ◽  
Wide Ph Range ◽  
Order Kinetic Model

Abstract In this study, we provide the first documented removal of humic acid (HA) from aqueous solution using polyacrylamide/chitosan (PAAm/CS) semi-IPN hydrogel. The prepared semi-IPN hydrogel was characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR). The factors effecting HA adsorption performance were individually tested, including initial pH, ionic strength, contact time, initial HA concentration, and temperature. The results indicated that semi-IPN hydrogel was successfully fabricated and can be applied in a wide pH range, from 3 to 9. Low ionic strength effectively enhanced the adsorption capacity. As the ionic strength increased, this enhancement was less obvious but still positive. The adsorption kinetics were fitted to a pseudo-first-order kinetic model, and the adsorption isotherm was described using the Sips isotherm model. The HA adsorption capacity increased with increasing temperature. The maximum adsorption capacity has the potential to attain 166.30 mg g−1, based on the Sips isotherm at 25 °C. Experiments demonstrated that the HA adsorption process can be primarily attributed to electrostatic interactions, and hydrogen bonding was also involved. Facile synthesis and good adsorptive performance indicate that semi-IPN hydrogel can be used for removing HA from water.

scholarly journals Adsorptive and Coagulative Removal of Trace Metals from Water Using Surface Modified Sawdust-Based Cellulose Nanocrystals

J ◽  
2021 ◽  
Vol 4 (2) ◽  
pp. 193-205
Author(s):  
Opeyemi A. Oyewo ◽  
Sam Ramaila ◽  
Lydia Mavuru ◽  
Taile Leswifi ◽  
Maurice S. Onyango
Keyword(s):  
Trace Metals ◽  
Adsorption Capacity ◽  
Cellulose Nanocrystals ◽  
Inductively Coupled Plasma ◽  
Electrostatic Interactions ◽  
Natural Waters ◽  
Maximum Adsorption Capacity ◽  
Solution Ph ◽  
Major Drawback ◽  
Surface Modified

The presence of toxic metals in surface and natural waters, even at trace levels, poses a great danger to humans and the ecosystem. Although the combination of adsorption and coagulation techniques has the potential to eradicate this problem, the use of inappropriate media remains a major drawback. This study reports on the application of NaNO2/NaHCO3 modified sawdust-based cellulose nanocrystals (MCNC) as both coagulant and adsorbent for the removal of Cu, Fe and Pb from aqueous solution. The surface modified coagulants, prepared by electrostatic interactions, were characterized using Fourier transform infrared, X-ray diffraction (XRD), and scanning electron microscopy/energy-dispersive spectrometry (SEM/EDS). The amount of coagulated/adsorbed trace metals was then analysed using inductively coupled plasma atomic emission spectroscopy (ICP-AES). SEM analysis revealed the patchy and distributed floccules on Fe-flocs, which was an indication of multiple mechanisms responsible for Fe removal onto MCNC. A shift in the peak position attributed to C2H192N64O16 from 2θ = 30 to 24.5° occurred in the XRD pattern of both Pb- and Cu-flocs. Different process variables, including initial metal ions concentration (10–200 mg/L), solution pH (2–10), and temperature (25–45 °C) were studied in order to investigate how they affect the reaction process. Both Cu and Pb adsorption followed the Langmuir isotherm with a maximum adsorption capacity of 111.1 and 2.82 mg/g, respectively, whereas the adsorption of Fe was suggestive of a multilayer adsorption process; however, Fe Langmuir maximum adsorption capacity was found to be 81.96 mg/g. The sequence of trace metals removal followed the order: Cu > Fe > Pb. The utilization of this product in different water matrices is an effective way to establish their robustness.

scholarly journals Characterization of Virus Adsorption by Using DEAE-Sepharose and Octyl-Sepharose

2002 ◽  
Vol 68 (8) ◽  
pp. 3965-3968 ◽  
Author(s):  
Patricia A. Shields ◽  
Samuel R. Farrah
Keyword(s):  
Sodium Chloride ◽  
Electrostatic Interactions ◽  
Hydrophobic Interactions ◽  
Chloride Concentration ◽  
Sodium Chloride Concentration ◽  
Virus Adsorption ◽  
Nacl Concentration

ABSTRACT Viruses were characterized by their adsorption to DEAE-Sepharose or by their elution from octyl-Sepharose by using buffered solutions of sodium chloride with different ionic strengths. Viruses whose adsorption to DEAE-Sepharose was reduced most rapidly by an increase in the sodium chloride concentration were considered to have the weakest electrostatic interactions with the solids; these viruses included MS2, E1, and φX174. Viruses whose adsorption to DEAE-Sepharose was reduced least rapidly were considered to have the strongest electrostatic interactions with the column; these viruses included P1, T4, T2, and E5. All of the viruses studied adsorbed to octyl-Sepharose in the presence of 4 M NaCl. Viruses that were eluted most rapidly following a decrease in the concentration of NaCl were considered to have the weakest hydrophobic interactions with the column; these viruses included φX174, CB4, and E1. Viruses that were eluted least rapidly from the columns after the NaCl concentration was decreased were considered to have the strongest hydrophobic interactions with the column; these viruses included f2, MS2, and E5.

scholarly journals Assay and physicochemical characterization of the antiparasitic albendazole

2012 ◽  
Vol 48 (2) ◽  
pp. 281-290 ◽  
Author(s):  
Noely Camila Tavares Cavalcanti ◽  
Giovana Damasceno Sousa ◽  
Maria Alice Maciel Tabosa ◽  
José Lamartine Soares Sobrinho ◽  
Leila Bastos Leal ◽  
...  
Keyword(s):  
Physicochemical Characterization ◽  
Analytical Techniques ◽  
Assay Method ◽  
Active Pharmaceutical Ingredients ◽  
X Ray Diffraction ◽  
Melting Points ◽  
X Ray ◽  
Pharmaceutical Ingredients ◽  
Complementary Techniques

The aim of this study was to characterize three batches of albendazole by pharmacopeial and complementary analytical techniques in order to establish more detailed specifications for the development of pharmaceutical forms. The ABZ01, ABZ02, and ABZ03 batches had melting points of 208 ºC, 208 ºC, and 209 ºC, respectively. X-ray diffraction revealed that all three batches showed crystalline behavior and the absence of polymorphism. Scanning electron microscopy showed that all the samples were crystals of different sizes with a strong tendency to aggregate. The samples were insoluble in water (5.07, 4.27, and 4.52 mg mL-1, respectively) and very slightly soluble in 0.1 M HCl (55.10, 56.90, and 61.70 mg mL-1, respectively) and additionally showed purities within the range specified by the Brazilian Pharmacopoeia 5th edition (F. Bras. V; 98% to 102%). The pharmacopeial assay method was not reproducible and some changes were necessary. The method was validated and showed to be selective, specific, linear, robust, precise, and accurate. From this characterization, we concluded that pharmacopeial techniques alone are not able to detect subtle differences in active pharmaceutical ingredients; therefore, the use of other complementary techniques is required to ensure strict quality control in the pharmaceutical industry.

scholarly journals Adsorción del naranja de metilo en solución acuosa sobre hidróxidos dobles laminares

2015 ◽  
Vol 25 (3) ◽  
pp. 25-34 ◽  
Author(s):  
Laura Alicia Ramírez Llamas ◽  
Araceli Jacobo Azuara ◽  
J. Merced Martínez Rosales
Keyword(s):  
Methyl Orange ◽  
Adsorption Capacity ◽  
Dye Adsorption ◽  
Temperature Programmed Desorption ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Suitable Temperature ◽  
Temperature Programmed ◽  
Double Hydroxides

In this paper, layered double hydroxides (LDH) were synthesized and characterized using techniques of Physisorption of Nitrogen, Infrared, Temperature Programmed Desorption, X-Ray Diffraction, TGA and Immersion Microcalorimetry, in order to determine the basic properties of the adsorbent. The methyl orange (MO) is used as a dye and as a result, it is frequently found in effluents from textile industries. The dye adsorption isotherms on LDH were studied as function of pH and temperature. The maximum adsorption capacity of methyl orange on LDH was carried out at pH 5, and the minimum adsorption capacity at pH 11, being 40.2 mg/g and 22.1 mg/g, respectively. Furthermore, the suitable temperature to promote the adsorption of methyl orange on LDH was at 25 °C, as at 35 °C shows a significant decrease. 

scholarly journals Silica-Coated Magnetic Nanocomposites for Pb2+ Removal from Aqueous Solution

2020 ◽  
Vol 10 (8) ◽  
pp. 2726 ◽  
Author(s):  
Roxana Nicola ◽  
Otilia Costişor ◽  
Mihaela Ciopec ◽  
Adina Negrea ◽  
Radu Lazău ◽  
...  
Keyword(s):  
Iron Oxide ◽  
Adsorption Capacity ◽  
Aqueous Media ◽  
Physical Stability ◽  
Absorption Capacity ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
Similar Materials ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Magnetic iron oxide-silica shell nanocomposites with different iron oxide/silica ratio were synthesized and structurally characterized by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), small-angle neutron scattering, magnetic and N2-sorption studies. The composite that resulted with the best properties in terms of contact surface area and saturation of magnetization was selected for Pb2+ adsorption studies from aqueous media. The material presented good absorption capacity (maximum adsorption capacity 14.9 mg·g−1) comparable with similar materials presented in literature. Its chemico-physical stability and adsorption capacity recommend the nanocomposite as a cheap adsorbent material for lead.

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