Removal of Rhodamine B from aqueous solution using magnetic NiFe nanoparticles

2015 ◽  
Vol 72 (7) ◽  
pp. 1243-1249 ◽  
Author(s):  
Yan Liu ◽  
Kaige Liu ◽  
Lin Zhang ◽  
Zhaowen Zhang
Keyword(s):  
Aqueous Solution ◽  
Rhodamine B ◽  
Order Kinetic ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Alloy Particles ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Face Centered ◽  
Surface Modified

Surface-modified magnetic nano alloy particles Ni2.33Fe were prepared using a hydrothermal method and they were utilized for removing Rhodamine B (RhB) from aqueous solution. The magnetic nanoparticles were characterized by X-ray diffraction, scanning electron microscopy, thermogravimetric analysis and Fourier transform infrared spectroscopy, which confirmed that the surface of the magnetic product with a face-centered cubic-type structure was successfully modified by sodium citrate. Kinetics studies were conducted. The pseudo-second-order kinetic model was used for fitting the kinetic data successfully. The Freundlich and Langmuir adsorption models were employed for the mathematical description of adsorption equilibrium. It was found that the adsorption isotherm can be very satisfactorily fitted by the Freundlich model.

scholarly journals In situ synthesis of layered double hydroxides on γ-Al2O3 and its application in chromium(VI) removal

2017 ◽  
Vol 75 (6) ◽  
pp. 1466-1473 ◽  
Author(s):  
Shifeng Li ◽  
Fang Qi ◽  
Min Xiao ◽  
Hongtao Fan ◽  
Yanming Shen ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Layered Double Hydroxides ◽  
Adsorptive Capacity ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Chromium Vi ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Double Hydroxides

Mg-Al layered double hydroxides (LDHs) adsorbent was synthesized in situ on γ-Al2O3 for the removal of Cr(VI) from aqueous solution. The material was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy, Raman spectroscopy, scanning electronic microscopy and thermogravimetry and differential thermal analysis. Compared to the LDHs powder, the calcined LDHs sorbent prepared in situ on γ-Al2O3 had higher specific surface area and was easy to recover and reuse. The adsorptive capacity for removing Cr(VI) from aqueous solution was resulting from the memory effect of LDHs based on the XRD results. Both the pseudo-second-order kinetic model and the Langmuir model fit the experimental data well. Furthermore, the adsorbent exhibits excellent sorption–regeneration performances.

Study of interactions between rhodamine B and a beidellite-rich clay fraction

Clay Minerals ◽  
2020 ◽  
Vol 55 (2) ◽  
pp. 194-202
Author(s):  
Hamida Belhanafi ◽  
Abdellah Bakhti ◽  
Noureddine Benderdouche
Keyword(s):  
Rhodamine B ◽  
Clay Fraction ◽  
Fine Fraction ◽  
Sorption Process ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Order Kinetic Model ◽  
Fine Clay ◽  
Competing Cations ◽  
Pseudo Second Order

AbstractThe interaction between a basic dye, rhodamine B, and a separated fine fraction from natural clay was studied. Chemical analysis, X-ray diffraction and Fourier-transform infrared spectroscopy confirmed the predominance of beidellite in the fine clay fraction. The interaction of rhodamine B with the fine clay fraction showed that sorption was fast and followed a pseudo-second-order kinetic model. The comparison between sorbed rhodamine B amounts as a function of the various experimental parameters such as pH, sorbent mass, dye concentration and the presence of competing ions suggests that: (1) the sorption process is largely pH-dependent; (2) significant competition is observed between the dye and the Ca2+ and Mg2+ ions; (3) the sorption proceeds, principally, by a cation-exchange mechanism; and (4) the sorption capacity of the fine fraction in the presence of competing cations such as Ca2+ is ~0.28 mmol g–1.

scholarly journals Removal of Rhodamine B from aqueous solution by ZnFe2O4 nanocomposite with magnetic separation performance

2017 ◽  
Vol 19 (4) ◽  
pp. 65-74 ◽  
Author(s):  
Wojciech Konicki ◽  
Daniel Siber ◽  
Urszula Narkiewicz
Keyword(s):  
Aqueous Solution ◽  
Kinetic Model ◽  
Adsorption Capacity ◽  
Rhodamine B ◽  
Second Order ◽  
Isotherm Models ◽  
Separation Performance ◽  
Order Kinetic ◽  
Order Kinetic Model ◽  
Pseudo Second Order

Abstract Magnetic ZnFe2O4 nanocomposite (ZnFe-NC) was used as an adsorbent for the removal of Rhodamine B (RB) from aqueous solution. The synthesized nanocomposite was characterized by XRD, SEM, HRTEM, BET and FTIR. The effects of various parameters such as initial RB concentration (5–25 mg L−1), pH (3.4–11.1) and temperature (20–60°C) were investigated. The adsorption capacity at equilibrium increased from 5.02 to 9.83 mg g−1, with the increase in the initial concentration of RB from 5 to 25 mg L−1 at pH 7.0 and at 20°C. The experimental results indicated that the maximum RB removal could be attained at a solution pH of 4.4 and the adsorption capacity obtained was 6.02 mg g−1. Kinetic adsorption data were analyzed using the pseudo-first-order kinetic model, the pseudo-second-order model and the intraparticle diffusion model. The adsorption kinetics well fitted using a pseudo-second-order kinetic model. The experimental isotherm data were analyzed using two isotherm models, namely, Langmuir and Freundlich. The results revealed that the adsorption behavior of the RB onto ZnFe-NC fitted well with the Langmuir isotherm model. In addition, various thermodynamic parameters, such as standard Gibbs free energy (ΔG°), enthalpy (ΔH°) and entropy (ΔS°) have been calculated.

scholarly journals Synthesis and application of surface-modified NiFe nanoparticles as a new magnetic nano adsorbent for the removal of nickel ions from aqueous solution

2017 ◽  
Vol 76 (10) ◽  
pp. 2851-2857 ◽  
Author(s):  
Yan Liu ◽  
Xiaoyi Shen
Keyword(s):  
Aqueous Solution ◽  
Sodium Citrate ◽  
Diffusion Processes ◽  
Order Kinetic ◽  
Adsorption Models ◽  
Freundlich Model ◽  
Nickel Ions ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Surface Modified

Abstract Surface-modified magnetic Ni2.33Fe alloy nanoparticles were prepared using a hydrothermal method. Thermogravimetric analysis (TG) and Fourier transform infrared spectroscopy (FTIR) tests demonstrated that the surface was successfully modified by sodium citrate. The surface-modified particles can be used for removing nickel ions from aqueous solution. The adsorption kinetics studies were performed and the pseudo-second-order kinetic model successfully described the kinetic data. The diffusion model indicated the adsorption was regulated by both surface and intraparticle diffusion processes. The Freundlich and Langmuir adsorption models were adopted for the mathematical description of adsorption equilibrium, and it was found that the experimental data fitted very well to the Freundlich model.

Adsorption Characteristics of Phenol in Aqueous Solution by Pinus massoniana Biochar

2013 ◽  
Vol 295-298 ◽  
pp. 1154-1160 ◽  
Author(s):  
Guo Zhi Deng ◽  
Xue Yuan Wang ◽  
Xian Yang Shi ◽  
Qian Qian Hong
Keyword(s):  
Aqueous Solution ◽  
Ph Value ◽  
Pinus Massoniana ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Adsorbent Dosage ◽  
Salt Ions ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The objective of this paper is to investigate the feasibility of phenol adsorption from aqueous solution by Pinus massoniana biochar. Adsorption conditions, including contact time, initial phenol concentration, adsorbent dosage, strength of salt ions and pH, have been investigated by batch experiments. Equilibrium can be reached in 24 h for phenol from 50 to 250 mg• L-1. The optimum pH value for this kind of biochar is 5.0. The amount of phenol adsorbed per unit decreases with the increase in adsorbent dosage. The existence of salt ions makes negligible influence on the equilibrium adsorption capacity. The experimental data is analyzed by the Freundlich and Langmuir isotherm models. Equilibrium data fits well to the Freundlich model. Adsorption kinetics models are deduced and the pseudo-second-order kinetic model provides a good correlation for the adsorbent process. The results show that the Pinus massoniana biochar can be utilized as an effective adsorption material for the removal of phenol from aqueous solution.

scholarly journals Insights into Starch Coated Nanozero Valent Iron-Graphene Composite for Cr(VI) Removal from Aqueous Medium

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Prasanna Kumarathilaka ◽  
Vimukthi Jayaweera ◽  
Hasintha Wijesekara ◽  
I. R. M. Kottegoda ◽  
S. R. D. Rosa ◽  
...  
Keyword(s):  
Point Of Zero Charge ◽  
Inert Material ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Graphene Composite ◽  
Removal Capacity ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
First Time

Embedding nanoparticles into an inert material like graphene is a viable option since hybrid materials are more capable than those based on pure nanoparticulates for the removal of toxic pollutants. This study reports for the first time on Cr(VI) removal capacity of novel starch stabilized nanozero valent iron-graphene composite (NZVI-Gn) under different pHs, contact time, and initial concentrations. Starch coated NZVI-Gn composite was developed through borohydrate reduction method. The structure and surface of the composite were characterized by scanning electron microscopy (SEM), X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), and point of zero charge (pHpzc). The surface area and pHpzc of NZVI-Gn composite were reported as 525 m2 g−1 and 8.5, respectively. Highest Cr(VI) removal was achieved at pH 3, whereas 67.3% was removed within first few minutes and reached its equilibrium within 20 min obeying pseudo-second-order kinetic model, suggesting chemisorption as the rate limiting process. The partitioning of Cr(VI) at equilibrium is perfectly matched with Langmuir isotherm and maximum adsorption capacity of the NZVI-Gn composite is 143.28 mg g−1. Overall, these findings indicated that NZVI-Gn composite could be utilized as an efficient and magnetically separable adsorbent for removal of Cr(VI).

Adsorption of Chromium (VI) from Aqueous Solution by Agricultural Waste Derived Activated Carbon

2013 ◽  
Vol 726-731 ◽  
pp. 2100-2106 ◽  
Author(s):  
Hua Zhang ◽  
Xue Hong Zhang ◽  
Yi Nian Zhu ◽  
Shou Rui Yuan
Keyword(s):  
Aqueous Solution ◽  
Activated Carbon ◽  
Agricultural Waste ◽  
Order Kinetic ◽  
Chromium Vi ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Grapefruit Peel ◽  
Pseudo Second Order ◽  
C 30

Activated carbon prepared from grapefruit peel, an agricultural solid waste by-product, has been used for the adsorption of Cr(VI) from aqueous solution. The effects of adsorbent dosage, pH and temperature on adsorption of Cr(VI) were investigated. The maximum adsorption yield was obtained at the initial pH of 3. The dynamical data fit very well with the pseudo-second-order kinetic model and the calculated adsorption capacities (23.98, 24.33 and 24.81 mg/g) were in good agreement with experiment results at 20°C, 30°C and 40 °C for the 100 mg/L Cr(VI) solution. The Freundlich model (R2 values were 0.9198-0.9871) fitted adsorption data better than the Langmuir model. The calculated parameters confirmed the favorable adsorption of Cr(VI) on the activated carbon prepared from grapefruit peel.

scholarly journals Simultaneous removal of cationic and anionic dyes from aqueous solution by double functional groups modified bagasse

2020 ◽  
Vol 82 (10) ◽  
pp. 2159-2167
Author(s):  
Ru-yi Zhou ◽  
Jun-xia Yu ◽  
Ru-an Chi
Keyword(s):  
Aqueous Solution ◽  
Functional Groups ◽  
Order Kinetic ◽  
Anionic Dyes ◽  
Adsorption Capacities ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Amine Groups ◽  
Modified Adsorbents ◽  
Zeta Potential Analysis

Abstract Double functional groups modified bagasse (DFMBs), a series of new zwitterionic groups of carboxyl and amine modified adsorbents, were prepared through grafting tetraethylenepentamine (TEPA) onto the pyromellitic dianhydride (PMDA) modified bagasse using the DCC/DMAP method. DFMBs' ability to simultaneously remove basic magenta (BM, cationic dye) and Congo red (CR, anionic dye) from aqueous solution in single and binary dye systems was investigated. FTIR spectra and Zeta potential analysis results showed that PMDA and TEPA were successfully grafted onto the surface of bagasse, and the ratio of the amount of carboxyl groups and amine groups was controlled by the addition of a dosage of TEPA. Adsorption results showed that adsorption capacities of DFMBs for BM decreased while that for CR increased with the increase of the amount of TEPA in both single and binary dye systems, and BM or CR was absorbed on the modified biosorbents was mainly through electrostatic attraction and hydrogen bond. The adsorption for BM and CR could reach equilibrium within 300 min, both processes were fitted well by the pseudo-second-order kinetic model. The cationic and anionic dyes removal experiment in the binary system showed that DMFBs could be chosen as adsorbents to treat wastewater containing different ratios of cationic and anionic dyes.

scholarly journals Study on the adsorption of methylene blue from aqueous solution using hydrogel glucomannan/graphene oxide

2021 ◽  
Vol 10 (1) ◽  
pp. 59-66
Author(s):  
Son Le Lam ◽  
Phu Nguyen Vinh ◽  
Hieu Le Trung ◽  
Tan Le Thua ◽  
Nhan Dang Thi Thanh ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Methylene Blue ◽  
Graphene Oxide ◽  
Adsorption Capacity ◽  
Organic Dyes ◽  
Dye Adsorption ◽  
Order Kinetic ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order

Glucomannan/graphene oxide (GM/GO) hydrogel was synthesized by using calcium hydroxide as the crosslinker. The synthesized material was characterized by using IR, XRD, SEM, EDX and RAMAN technology. The composite hydrogel was used for removal of organic dyes from aqueous solution. The results showed that the GM/GO hydrogel had a porous structure and a high adsorption capacity toward methylene blue (MB). The pseudo-second-order kinetic model could fit the rate equation of MB adsorption onto the GM/GO hydrogel. The adsorption of MB onto GM/GO hydrogel was a spontaneous process. In addition, the equilibrium adsorption isotherm data indicated that equilibrium data were fitted to the Langmuir isotherm and the maximum dye adsorption capacity was 198,69 mg.g-1. Moreover, the hydrogel was stable and easily recovered and adsorption capacity was around 97% of the initial saturation adsorption capacity after being used five times.

scholarly journals The Removal of Uranium and Thorium from Their Aqueous Solutions by 8-Hydroxyquinoline Immobilized Bentonite

Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Langmuir Isotherm ◽  
Freundlich Isotherm ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The sorption of uranium and thorium from their aqueous solutions by using 8-hydroxyquinoline modified Na-bentonite (HQ-bentonite) was investigated by the batch technique. Na-bentonite and HQ-bentonite were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier Transform Infrared (FTIR) spectroscopy. Factors that influence the sorption of uranium and thorium onto HQ-bentonite such as solution pH, contact time, initial metal ions concentration, HQ-bentonite mass, and temperature were tested. Sorption experiments were expressed by Freundlich and Langmuir isotherms and the sorption results demonstrated that the sorption of uranium and thorium onto HQ-bentonite correlated better with the Langmuir isotherm than the Freundlich isotherm. Kinetics studies showed that the sorption followed the pseudo-second-order kinetic model. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° indicated that the sorption of uranium and thorium onto HQ-bentonite was endothermic, feasible, spontaneous, and physical in nature. The maximum adsorption capacities of HQ-bentonite were calculated from the Langmuir isotherm at 303 K and were found to be 63.90 and 65.44 for U(VI) and Th(IV) metal ions, respectively.

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