Equilibrium study of adsorption of L-cysteine by natural bentonite

Clay Minerals ◽  
2009 ◽  
Vol 44 (1) ◽  
pp. 125-133 ◽  
Author(s):  
H. Faghihian ◽  
M. Nejati-Yazdinejad
Keyword(s):  
Adsorption Process ◽  
Raw Materials ◽  
Ph Dependence ◽  
Langmuir Model ◽  
X Ray Diffraction ◽  
X Ray ◽  
Equilibrium Study ◽  
Surface Sites ◽  
Adsorption Data ◽  
Adsorption Processes

AbstractL-cysteine (Cys) was adsorbed by bentonite (Ben) from aqueous solutions of variable concentrations and pHs. The raw materials and the adsorbed molecules (Ben-Cys) were characterized using X-ray diffraction (XRD), infrared spectroscopy (IR), thermal analysis methods (TG, DTG and DSC). The results indicated that the adsorption process depended strongly on pH, temperature and concentration of amino acid. Cysteine is specifically adsorbed on bentonite surface sites, probably through its NH3+ moiety. The pH dependence suggests that these sites may be silanolate groups (≡Si-O–). It is presumed that ion exchange interaction governs the adsorption process. The experimental data of adsorption isotherms obtained and analysed with the Langmuir model showed that this model fitted the adsorption data. Calculated thermodynamic parameters (ΔHº, ΔSº, and ΔGº) indicate that the adsorption processes were exothermic.

Adsorption Removal of Ni(II) from Aqueous Solution by Raw and Acid-Activated Kaolinite

2013 ◽  
Vol 781-784 ◽  
pp. 2269-2272 ◽  
Author(s):  
Shi Yong Wei ◽  
Xu Hong Deng
Keyword(s):  
Cation Exchange Capacity ◽  
Negative Charge ◽  
Physical Adsorption ◽  
Exchange Capacity ◽  
Langmuir Model ◽  
Batch Adsorption ◽  
X Ray Diffraction ◽  
X Ray ◽  
Adsorption Removal ◽  
Adsorption Data

X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen physical adsorption, potentiometric titrations and batch adsorption experiments were employed to characterize the crystal structure, micromorphologies and surface properties of raw kaolinite (RKao) and acid-activated kaolinite (AAKao). Compared to RKao, the particle size of AAKao became smaller, but the specific surface area (SSA), cation exchange capacity (CEC) and surface negative charge at pH 5.5 increased. The adsorption capacity (qmax) for Ni (II) of RKao and AAKao was 3.25 mg/g and 5.09 mg/g, respectively. The adsorption data for Ni (II) by RKao and AAKao could be fitted by Langmuir model (R2 =0.991 and 0.989, respectively).

scholarly journals Removal And Regeneration of As(V) In Aqueous Solutions By Adsorption On Calcined Fluorapatite: Kinetics And Thermodynamic Parameters.

2021 ◽  
Author(s):  
Rachid EL Kaim Billah ◽  
Savaş Kaya ◽  
Selçuk Şimşek ◽  
El Mahdi Halim ◽  
Mahfoud Agunaou ◽  
...  
Keyword(s):  
Adsorption Process ◽  
Regression Coefficient ◽  
Mass Effect ◽  
Significant Loss ◽  
X Ray Diffraction ◽  
X Ray ◽  
Langmuir Adsorption ◽  
Adsorption Data ◽  
Pseudo Second Order ◽  
Effect Time

Abstract In this work, Fluorapatite has been prepared and successfully applied for the removal of As (VI). The materials prepared have been characterized using X-ray diffraction (XRD), infrared transform transform spectroscopy. Fourier (FTIR), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). Thermogravimetric analysis (TGA) and zero load point pH (pHPZC) were also considered as part of these characterizations. In this work, several parameters affecting the adsorption process were studied, such as: the mass effect, time, pH, and the initial concentration effect. The value of the regression coefficient showed that the data The experimental results corresponded best to the pseudo-second order (PSO) model, while the Langmuir adsorption isotherms best described the equilibrium adsorption data with the highest qm of 43.10 mg / g. Finally, FapC has been successfully reused for more than 5 cycles without significant loss of its sorption capacity.

scholarly journals Weathered Sand of Basalt as a Potential Nickel Adsorbent

Processes ◽  
2020 ◽  
Vol 8 (10) ◽  
pp. 1238
Author(s):  
Jae Hong Park ◽  
Jae Kwan Lee
Keyword(s):  
Adsorption Process ◽  
Sem Analysis ◽  
Langmuir Model ◽  
X Ray Diffraction ◽  
Order Model ◽  
X Ray ◽  
Freundlich Isotherms ◽  
Freundlich Equation ◽  
Low Concentrations ◽  
Pseudo Second Order

The natural mineral, weathered sand of basalt (WSB), was utilized to investigate whether nickel can be removed. X-ray diffraction (XRD) and scanning electron microscopy (SEM) analysis were performed to characterize WSB. The effects of various conditions, i.e., contact time, pH, WSB dosage, particle size of WSB, and temperature were analyzed. The experimental data were analyzed by two widely used equations, i.e., Langmuir and Freundlich isotherms. The results obtained revealed that the WSB adsorption process was more consistent with the Langmuir model than the Freundlich equation. The kinetics data fitted well into the pseudo-second-order model. The findings of the present study indicate that WSB could be used for removing nickel from aqueous solution. Moreover, its concentration can be reduced from 1.0 mg/L to ND (not detected, below the device limit <0.01 μg/L) under the optimal condition. Therefore, WSB is considered to be usable as one of the adsorbents for nickel removal in water. In addition, since heavy metals are often present in low concentrations in water, it is considered that WSB can be applied as one of the effective alternatives for removing low-concentration nickel.

scholarly journals Waste and Solar Energy: An Eco-Friendly Way for Glass Melting

2021 ◽  
Vol 5 (2) ◽  
pp. 16
Author(s):  
Isabel Padilla ◽  
Maximina Romero ◽  
José I. Robla ◽  
Aurora López-Delgado
Keyword(s):  
Solar Energy ◽  
Environmental Sustainability ◽  
Raw Materials ◽  
Glass Melting ◽  
Glass Network ◽  
X Ray Diffraction ◽  
X Ray ◽  
Concentrated Solar Energy ◽  
Calcium Source ◽  
The Aluminum Industry

In this work, concentrated solar energy (CSE) was applied to an energy-intensive process such as the vitrification of waste with the aim of manufacturing glasses. Different types of waste were used as raw materials: a hazardous waste from the aluminum industry as aluminum source; two residues from the food industry (eggshell and mussel shell) and dolomite ore as calcium source; quartz sand was also employed as glass network former. The use of CSE allowed obtaining glasses in the SiO2-Al2O3-CaO system at exposure time as short as 15 min. The raw materials, their mixtures, and the resulting glasses were characterized by means of X-ray fluorescence, X-ray diffraction, and differential thermal analysis. The feasibility of combining a renewable energy, as solar energy and different waste for the manufacture of glasses, would highly contribute to circular economy and environmental sustainability.

scholarly journals Mining Wastes of an Albite Deposit as Raw Materials for Vitrified Mullite Ceramics

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 232
Author(s):  
Pedro J. Sánchez-Soto ◽  
Eduardo Garzón ◽  
Luis Pérez-Villarejo ◽  
George N. Angelopoulos ◽  
Dolores Eliche-Quesada
Keyword(s):  
Particle Size ◽  
Raw Materials ◽  
Phase Evolution ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Mining Wastes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Maximum Value

In this work, an examination of mining wastes of an albite deposit in south Spain was carried out using X-ray Fluorescence (XRF), X-ray diffraction (XRD), particle size analysis, thermo-dilatometry and Differential Thermal Analysis (DTA) and Thermogravimetric (TG) analysis, followed by the determination of the main ceramic properties. The albite content in two selected samples was high (65–40 wt. %), accompanied by quartz (25–40 wt. %) and other minor minerals identified by XRD, mainly kaolinite, in agreement with the high content of silica and alumina determined by XRF. The content of Na2O was in the range 5.44–3.09 wt. %, being associated with albite. The iron content was very low (<0.75 wt. %). The kaolinite content in the waste was estimated from ~8 to 32 wt. %. The particle size analysis indicated values of 11–31 wt. % of particles <63 µm. The ceramic properties of fired samples (1000–1350 °C) showed progressive shrinkage by the thermal effect, with water absorption and open porosity almost at zero at 1200–1250 °C. At 1200 °C, the bulk density reached a maximum value of 2.38 g/cm3. An abrupt change in the phase evolution by XRD was found from 1150 to 1200 °C, with the disappearance of albite by melting in accordance with the predictions of the phase diagram SiO2-Al2O3-Na2O and the system albite-quartz. These fired materials contained as main crystalline phases quartz and mullite. Quartz was present in the raw samples and mullite was formed by decomposition of kaolinite. The observation of mullite forming needle-shape crystals was revealed by Scanning Electron Microscopy (SEM). The formation of fully densified and vitrified mullite materials by firing treatments was demonstrated.

Facile Solid State Method Route Synthesis and Enhance Visible Light Activities of BiVO4 by Doping Co

2016 ◽  
Vol 703 ◽  
pp. 316-320
Author(s):  
Hai Feng Chen ◽  
Jing Ling Hu ◽  
Bing Xu
Keyword(s):  
Solid State ◽  
Visible Light ◽  
Catalytic Effect ◽  
Catalytic Properties ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Solid State Method ◽  
Illumination Time ◽  
X Ray ◽  
State Method

Using NH4VO3, Bi (NO3)3•5H2O and Co (NO3)2•6H2O as raw materials, Co doped BiVO4 (Co/BiVO4) photocatalysts were successfully prepared by solid state method. And the photo catalytic properties were test in this work. Crystal structures of these samples were characterized by X-ray diffraction (XRD). The Methyl Orange (MO) was simulated as the sewage under the visible light to explorer the influence of the illumination time and the mass of photocatalyst. The visible-light absorption spectrum of BiVO4 was broadening with doping Co. It was found that the Co/BiVO4 had higher photocatalytic activity than pure BiVO4 .The reason of enhanced catalytic effect also had been analyzed and discussed in the article.

The Roman Ceramics of Salobrena (Granada-Spain) and their Raw Materials

1992 ◽  
Vol 267 ◽  
Author(s):  
Ana M De Andres ◽  
Isabel MuÑOZ
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Raw Materials ◽  
Third Century ◽  
Western Coast ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Third ◽  
Good Number ◽  
Scanning Electron

ABSTRACTNineteen roman ceramic sherds found near Salobreña (Granada, Spain), in the western coast of the Mediterranean Sea, as well as different ceramic clays from the surroundingsare studied. Both clays and ceramic sherds are characterizad by X-ray diffraction and spectrometry, differential thermal analysis, and scanning electron and optical microscopies. A good number of the ceramic pieces, among which some “Terrae Sigillatae”, have a composition similar to that of the local clays and, thus, have been probably manufactured at Salobreña. Only a few of them have a foreign origin. For most of them, the firing temperature was about 800-850 °C, although some have been produced at 900-1000 °C, and some others at 1000-1100 °C. It is concluded that Salobreña appearsto have been an important settlement just in the third century of the Christian era.

Magnetic Properties of Bulk Zn0.95-XMnXFe0.05O2 Prepared by Sol-Gel Method and Subsequent Hot Pressing

2011 ◽  
Vol 268-270 ◽  
pp. 356-359 ◽  
Author(s):  
Wen Song Lin ◽  
C. H. Wen ◽  
Liang He
Keyword(s):  
Magnetic Properties ◽  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Sol Gel ◽  
Secondary Phase ◽  
X Ray Diffraction ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method ◽  
Doped Zno

Mn, Fe doped ZnO powders (Zn0.95-xMnxFe0.05O2, x≤0.05) were synthesized by an ameliorated sol-gel method, using Zn(CH3COO)2, Mn(CH3COO)2and FeCl2as the raw materials, with the addition of vitamin C as a kind of chemical reducer. The resulting powder was subsequently compacted under pressure of 10 MPa at the temperature of 873K in vacuum. The crystal structure and magnetic properties of Zn0.95-xMnxFe0.05O2powder and bulk samples have been investigated by X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). X-ray photoelectron spectroscopy (XPS) was used to study chemical valence of manganese, iron and zinc in the samples. The x-ray diffraction (XRD) results showed that Zn0.95-xMnxFe0.05O (x≤0.05) samples were single phase with the ZnO-like wurtzite structure. No secondary phase was found in the XRD spectrum. X-ray photoelectron spectroscopy (XPS) showed that Fe and Mn existed in Zn0.95-xMnxFe0.05O2samples in Fe2+and Mn2+states. The results of VSM experiment proved the room temperature ferromagnetic properties (RTFP) of Mn, Fe co-doped ZnO samples.

Solvothermal Synthesis of Bi2Se3 Hexagonal Nanosheet Crystals

2011 ◽  
Vol 236-238 ◽  
pp. 1712-1716 ◽  
Author(s):  
Hai Tao Liu ◽  
Jun Dai ◽  
Jia Jia Zhang ◽  
Wei Dong Xiang
Keyword(s):  
Electron Microscope ◽  
Solvothermal Synthesis ◽  
Solvothermal Method ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Scanning Electron

Bismuth selenide (Bi2Se3) hexagonal nanosheet crystals with uniform size were successfully prepared via a solvothermal method at 160°C for 22 h using bismuth trichloride(BiCl3) and selenium powder(Se) as raw materials, sodium bisulfite(NaHSO3) as a reducing agent, diethylene glycol(DEG) as solvent, and ammonia as pH regulator. Various techniques such as X-ray diffraction (XRD), field-emission scanning electron microscope (FESEM), high-resolution transmission electron microscope (HRTEM), and selected area electron diffraction (SAED) were used to characterize the obtained products. Results show that the as-synthesized samples are pure Bi2Se3 hexagonal nanosheet crystals. A possible growth mechanism for Bi2Se3 hexagonal nanosheet crystals is also discussed based on the experiment.

Synthesis of Spherical LiFePO4/C Composites as Cathode Material of Lithium-Ion Batteries by a Novel Glucose Assisted Hydrothermal Method

2013 ◽  
Vol 787 ◽  
pp. 58-64 ◽  
Author(s):  
Xiang Feng Li ◽  
Zhao Zhang ◽  
Fang Liu ◽  
Shu Ping Zheng
Keyword(s):  
Hydrothermal Method ◽  
Raw Materials ◽  
Lithium Ion ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
High Discharge ◽  
X Ray ◽  
High Discharge Capacity ◽  
Optimal Sample ◽  
Structure Morphology

The LiFePO4/C composites with different morphology are synthesized by a novel glucose assisted hydrothermal method at various glucose concentrations (from 0 to 0.25mol/L) and the insoluble lithium source Li2CO3, (NH4)2Fe (SO4)2·6H2O and (NH4)2HPO4(n (Li):n (Fe):n (P)=1:1:1) are used as raw materials. The structure, morphology, thermal performance and electrochemical properties of the synthesized composites are characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), thermogravimetry/differential scanning calorimetry (TG-DSC), galvanostatic charge/discharge tests and cyclic voltammetry (CV). The results show that the LiFePO4/C synthesized with 0.125mol/L glucose has the relatively small particles size (0.1~0.5μm) and the well spherical morphology. The optimal sample exhibits a high discharge capacity of 160.0mAh/g at the first cycle and exhibits a good reversibility and stability in CV tests.

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