scholarly journals Effective Removal of Malachite Green from Aqueous Solutions Using Magnetic Nanocomposite: Synthesis, Characterization, and Equilibrium Study

2021 ◽  
Vol 2021 ◽  
pp. 1-15
Author(s):  
Ali Q. Alorabi
Keyword(s):  
Surface Area ◽  
Malachite Green ◽  
Chemical Activation ◽  
Aqueous Media ◽  
Kinetic Studies ◽  
Cost Effective ◽  
Magnetic Nanocomposite ◽  
Bet Surface Area ◽  
Isotherm Models ◽  
Order Kinetic

In this work, magnetized activated Juniperus procera leaves (Fe3O4@AJPL) were successfully prepared via chemical activation of JPL and in situ coprecipitation with Fe3O4. A Fe3O4@AJPL nanocomposite was successfully applied for the elimination of malachite green (MG) dye from aqueous media. The prepared Fe3O4@AJPL adsorbent was characterized by SEM, EDX, TEM, XRD, FTIR, TGA, and BET surface area analyses. The BET surface area and pore size of the Fe3O4@AJPL nanocomposite were found to be 38.44 m2/g and 10.6 nm, respectively. The XRD and FTIR results indicated the formation of a Fe3O4@AJPL nanocomposite. Different parameters, such as pH of the solution (3–8), adsorbent dosage (10–100 mg), temperature (25–45°C), contact time (5-240 min), and initial MG concentrations (20–350 mg/L), for the elimination of the MG dye using Fe3O4@AJPL were optimized and found to be 7, 50 mg, 45°C, 120 min, and 150 mg/L, respectively. The nonlinear isotherm and kinetic studies exhibited a better fitting to second-order kinetic and Langmuir isotherm models, with a maximum monolayer adsorption capacity of 318.3 mg/g at 45°C, which was highly superior to the previously reported magnetic nanocomposite adsorbents. EDX analyses confirmed the presence of nitrogen on the Fe3O4@AJPL surface after MG adsorption. The calculated thermodynamic factors indicated endothermic and spontaneous processes. The desorption of MG dye from Fe3O4@AJPL was performed using a solution of 90% ethanol. Finally, it could be concluded that the designed Fe3O4@AJPL magnetic nanocomposite will be a cost-effective and promising adsorbent for the elimination of MG from aqueous media.

scholarly journals Unique Adsorption Properties of Malachite Green on Interlayer Space of Cu-Al and Cu-Al-SiW12O40 Layered Double Hydroxides

2020 ◽  
Vol 15 (3) ◽  
pp. 653-661
Author(s):  
Neza Rahayu Palapa ◽  
Novie Juleanti ◽  
Normah Normah ◽  
Tarmizi Taher ◽  
Aldes Lesbani
Keyword(s):  
Adsorption Capacity ◽  
Surface Area ◽  
Malachite Green ◽  
Interlayer Space ◽  
Interlayer Distance ◽  
Bet Surface Area ◽  
Order Kinetic ◽  
Pseudo Second Order ◽  
Double Hydroxide ◽  
Double Hydroxides

Cu-Al layered double hydroxide (LDH) was intercalated with Keggin ion of polyoxometalate           K4[a-SiW12O40] to form Cu-Al-SiW12O40 LDH. The obtained materials were analyzed by X-ray Diffraction (XRD), Fourier Transform Infra Red (FTIR) spectroscopy, and Brunaur-Emmett-Teller (BET) surface area analysis. Furthermore, the materials were used as adsorbents of malachite green from aqueous solution. Some variables for adsorption, such as: effect of adsorption times, malachite green concentration, and also adsorption temperature, were explored. The results showed that diffraction at 11.72° on Cu-Al LDH has interlayer distance of 7.56 Å. The intercalation of that LDH with [a-SiW12O40]4− ion resulted increasing interlayer distance to 12.10 Å. The surface area of material was also increased after intercalation from 46.2 m2/g to 89.02 m2/g. The adsorption of malachite green on Cu-Al and          Cu-Al-SiW12O40 LDHs followed pseudo second order kinetic and isotherm Langmuir model with adsorption capacity of Cu-Al and Cu-Al-SiW12O40 LDHs was 55.866 mg/g and 149.253 mg/g, respectively. That adsorption capacity is equal with increasing interlayer space and surface area properties of material after intercalation. Thus, the adsorption of malachite green on Cu-Al and Cu-Al-SiW12O40 LDHs is unique and dominantly occurred on interlayer space of LDH as active site adsorption. Copyright © 2020 BCREC Group. All rights reserved

scholarly journals GC/MS screening of buckthorn phytochemicals and their use to synthesize ZnO nanoparticles for photocatalytic degradation of malachite Green dye in water

2021 ◽  
Author(s):  
Ibrahem M. A. Hasan ◽  
Ahmed R. Tawfik ◽  
Fawzy H. Assaf
Keyword(s):  
Photocatalytic Degradation ◽  
Surface Area ◽  
Malachite Green ◽  
Uv Light ◽  
Aqueous Media ◽  
Total Pore Volume ◽  
Bet Surface Area ◽  
Zno Nps ◽  
Malachite Green Dye ◽  
Photodegradation Efficiency

Abstract Zinc oxide nanoparticles (ZnO NPs) were biosynthesized. According to GC/MS analysis, chalcone; the main phytochemical; is probably complexed with Zn ions that are then oxidized to ZnO NPs by atmospheric O2 during heating. The ZnO NPs were characterized by TG, FTIR, XRD, FESEM, TEM, eEDAX, and BET surface area analysis. Sphere-like ZnO NPs were formed with 11 nm mean crystallite size, 5.2 m2 g−1 surface area, and 0.02 cm3 g−1 total pore volume. The synthesized ZnO showed excellent photocatalytic degradation (96.5±0.24% in 1 hour at 25 °C) of malachite green (MG) in aqueous solutions under UV light at optimum conditions; pH 10, MG initial concentration of 20 mg L−1, and ZnO dose of 1.5 g L−1. Also, ZnO showed very good reusability (92.9± 0.2% after 5 runs). The experimental data obeyed pseudo-first-order kinetics (R2=0.92). The photocatalysis process is dependent on the following species in the order: OH. > electron/positive hole pairs > O2.−. Moreover, photodegradation efficiency decreased in the presence of CO32−, HCO3−, and Cl−, but increased in the presence of NO3−, and SO42− ions. Thus, the green synthesized ZnO NPs can be applied as an efficient photocatalyst for the removal of MG from aqueous media.

scholarly journals Chemical Modification of Combusted Coal Gangue for U(VI) Adsorption: Towards a Waste Control by Waste Strategy

2021 ◽  
Vol 13 (15) ◽  
pp. 8421
Author(s):  
Yuan Gao ◽  
Jiandong Huang ◽  
Meng Li ◽  
Zhongran Dai ◽  
Rongli Jiang ◽  
...  
Keyword(s):  
Structural Analysis ◽  
High Efficiency ◽  
Low Cost ◽  
Chemical Activation ◽  
Cost Effective ◽  
Coal Gangue ◽  
Order Kinetic ◽  
Practical Applications ◽  
Detailed Structural Analysis ◽  
Alkaline Conditions

Uranium mining waste causes serious radiation-related health and environmental problems. This has encouraged efforts toward U(VI) removal with low cost and high efficiency. Typical uranium adsorbents, such as polymers, geopolymers, zeolites, and MOFs, and their associated high costs limit their practical applications. In this regard, this work found that the natural combusted coal gangue (CCG) could be a potential precursor of cheap sorbents to eliminate U(VI). The removal efficiency was modulated by chemical activation under acid and alkaline conditions, obtaining HCG (CCG activated with HCl) and KCG (CCG activated with KOH), respectively. The detailed structural analysis uncovered that those natural mineral substances, including quartz and kaolinite, were the main components in CCG and HCG. One of the key findings was that kalsilite formed in KCG under a mild synthetic condition can conspicuous enhance the affinity towards U(VI). The best equilibrium adsorption capacity with KCG was observed to be 140 mg/g under pH 6 within 120 min, following a pseudo-second-order kinetic model. To understand the improved adsorption performance, an adsorption mechanism was proposed by evaluating the pH of uranyl solutions, adsorbent dosage, as well as contact time. Combining with the structural analysis, this revealed that the uranyl adsorption process was mainly governed by chemisorption. This study gave rise to a utilization approach for CCG to obtain cost-effective adsorbents and paved a novel way towards eliminating uranium by a waste control by waste strategy.

scholarly journals Fabrication of novel particle electrode γ-Al2O3@ZIF-8 and its application for degradation of Rhodamine B

2019 ◽  
Vol 80 (1) ◽  
pp. 109-116 ◽  
Author(s):  
Liguo Zhang ◽  
Caixia Ma ◽  
Lei Liu ◽  
Jingshi Pan ◽  
Qilin Wang
Keyword(s):  
Surface Area ◽  
Removal Efficiency ◽  
Rhodamine B ◽  
Three Dimensional ◽  
Cell Voltage ◽  
Bet Surface Area ◽  
Order Kinetic ◽  
Zeolitic Imidazolate Framework ◽  
Crystallization Method ◽  
Order Kinetic Model

Abstract Due to the high Brunauer–Emmett–Teller (BET) surface area of zeolitic imidazolate framework (ZIF)-8, a secondary crystallization method was used to prepare a particle electrode of γ-Al2O3@ZIF-8. According to the results from a field emission scanning electron microscope (SEM) and X-ray diffractometer (XRD), the particle electrode of γ-Al2O3 was successfully loaded with ZIF-8, and the BET surface area (1,433 m2/g) of ZIF-8 was over ten times that of γ-Al2O3. The key operation parameters of cell voltage, pH, initial RhB concentration and electrolyte concentration were all optimized. The observed rate constant (kobs) of the pseudo-first-order kinetic model for the electrocatalytic oxidation (ECO) system with the particle electrode of γ-Al2O3@ZIF-8 (15.2 × 10−2 min−1) was over five times higher than that of the system with the traditional particle electrode of γ-Al2O3 (2.6 × 10−2 min−1). The loading of ZIF-8 on the surface of γ-Al2O3 played an important role in improving electrocatalytic activity for the degradation of Rhodamine B (RhB), and the RhB removal efficiency of the three-dimensional (3D) electrocatalytic system with the particle electrode of γ-Al2O3@ZIF-8 was 93.5% in 15 min, compared with 27.5% in 15 min for the particle electrode of γ-Al2O3. The RhB removal efficiency was kept over 85% after five cycles of reuse for the 3D electrocatalytic system with the particle electrode of γ-Al2O3@ZIF-8.

scholarly journals Enhanced biosorption of Cr(VI) using cotton fibers coated with chitosan – role of ester bonds

2018 ◽  
Vol 78 (3) ◽  
pp. 476-486 ◽  
Author(s):  
Sergio I. Rojas ◽  
Diana C. Duarte ◽  
Sergio D. Mosquera ◽  
Felipe Salcedo ◽  
Juan P. Hinestroza ◽  
...  
Keyword(s):  
Hexavalent Chromium ◽  
Freundlich Isotherm ◽  
Kinetic Studies ◽  
Chitosan Solution ◽  
Cotton Fibers ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Amino Groups ◽  
Removal Capacity

Abstract We report on the role of ester bonds in the enhanced removal of hexavalent chromium from water using cotton fibers coated with chitosan. Adsorption capacities up to five times higher than those of the unmodified fibers were observed when the cotton fibers were exposed to an NaOH, followed by citric acid (0.97 M), and a chitosan solution (2%). We found that the use of NaOH favors the formation of ester bonds over amide bonds on the surface of the cotton fibers. This increase in the surface density of ester bonds generates an increase in the amount of exposed amino groups from the chitosan, hence increasing the removal capacity of the modified fibers. Experimental results also reveal that the adsorption is induced by the electrostatic attraction between the protonated amino groups on the surface and the negatively charged chromium ions in the water. Adsorption isotherms and kinetic studies indicated that the adsorption process fits the Langmuir and the Freundlich isotherm models as well as the pseudo-first and pseudo-second order kinetic models. These results can open a new avenue for the manufacturing of fibers with enhanced removal capacities for hexavalent chromium.

scholarly journals The Equilibrium, Kinetics, and Thermodynamics Studies of the Sorption of Methylene Blue from Aqueous Solution Using Pulverized Raw Macadamia Nut Shells

2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Joshua N. Edokpayi ◽  
Samson O. Alayande ◽  
Ahmed Adetoro ◽  
John O. Odiyo
Keyword(s):  
Aqueous Solution ◽  
Methylene Blue ◽  
Surface Area ◽  
Low Cost ◽  
Aqueous Media ◽  
Group Analysis ◽  
Second Order ◽  
Isotherm Models ◽  
Macadamia Nut ◽  
Pseudo Second Order

In this study, the potential for pulverized raw macadamia nut shell (MNS) for the sequestration of methylene blue from aqueous media was assessed. The sorbent was characterized using scanning electron microscopy for surface morphology, functional group analysis was performed with a Fourier-transform infrared spectrometer (FT-IR), and Brunauer–Emmett–Teller (BET) isotherm was used for surface area elucidation. The effects of contact time, sorbent dosage, particle size, pH, and change in a solution matrix were studied. Equilibrium data were fitted using Temkin, Langmuir, and Freundlich adsorption isotherm models. The sorption kinetics was studied using the Lagergren pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion models. The feasibility of the study was established from the thermodynamic studies. A surface area of 2.763 m2/g was obtained. The equilibrium and kinetics of sorption was best described by the Langmuir and the pseudo-second-order models, respectively. The sorption process was spontaneous (−ΔG0=28.72−31.77 kJ/mol) and endothermic in nature (ΔH0=17.45 kJ/mol). The positive value of ΔS0 (0.15 kJ/molK) implies increased randomness of the sorbate molecules at the surface of the sorbent. This study presents sustainable management of wastewater using MNS as a potential low-cost sorbent for dye decontamination from aqueous solution.

scholarly journals Waste phenolic resin derived activated carbon by microwave-assisted KOH activation and application to dye wastewater treatment

2019 ◽  
Vol 8 (1) ◽  
pp. 408-415 ◽  
Author(s):  
Wenhai Hu ◽  
Song Cheng ◽  
Hongying Xia ◽  
Libo Zhang ◽  
Xin Jiang ◽  
...  
Keyword(s):  
Wastewater Treatment ◽  
Activated Carbon ◽  
Surface Area ◽  
Adsorption Isotherms ◽  
Phenolic Resin ◽  
Bet Surface Area ◽  
Isotherm Models ◽  
Koh Activation ◽  
Activation Process ◽  
Dye Wastewater

Abstract The waste phenolic resin was utilized as the raw material to prepare activated carbon (AC) used KOH as the activating agent via microwave heating. The phenolic resin was carbonized at 500°C and then performed with a KOH/Char ratio of 4 and microwave power of 700 W for a duration of 15 min. The physic-chemical characteristics of the AC were characterized by N2 adsorption instrument, FTIR, SEM and TEM. The BET surface area and pore volume of AC were found to be 4269 m2/g and 2.396 ml/g, respectively. The activation process to generate such a phenomenally high surface area of the AC has little reported in open literatures and could pave way for preparation adsorbents that are far superior to the currently marketed adsorbents. The methylene blue (MB) was used as the model to assess its suitability to dye wastewater treatment. Towards this, the MB adsorption isotherms were conducted at three different temperatures and tested with different adsorption isotherm models. The adsorption isotherms could be modeled using Langmuir isotherm. While the kinetics could be used the pseudo-second order kinetics to describe. Thermodynamic results demonstrated that the adsorption process was a spontaneous, as well as an endothermic.

scholarly journals Parametric, equilibrium and kinetic studies on the removal of mercury using ion exchange resin

2017 ◽  
Vol 12 (2) ◽  
pp. 305-313 ◽  
Author(s):  
N. Rajamohan ◽  
M. Rajasimman
Keyword(s):  
Freundlich Isotherm ◽  
Kinetic Studies ◽  
Strong Acid ◽  
Ion Exchange Resin ◽  
Second Order ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Acid Cation ◽  
Pseudo Second Order ◽  
Langmuir Constants

This experimental research was an investigation into removal of mercury by using a strong acid cation resin, 001 × 7. Parametric experiments were conducted to determine the optimum pH, resin dosage, agitation speed and the effect of change in concentration in the range of 50–200 mg/L. High resin dosages favoured better removal efficiency but resulted in lower uptakes. Equilibrium experiments were performed and fitted to Langmuir and Freundlich isotherm models. Langmuir model suited well to this study confirming the homogeneity of the resin surface. The Langmuir constants were estimated as qmax = 110.619 mg/g and KL = 0.070 L/g at 308 K. Kinetic experiments were modeled using Pseudo second order model and higher values of R2 (>0.97) were obtained. The Pseudo second order kinetic constants, namely, equilibrium uptake (qe) and rate constant (k2), were evaluated as 59.17 mg/g and 40.2 × 10−4 g mg−1 min−1 at an initial mercury concentration of 100 mg/L and temperature of 308 K.

scholarly journals Orthophosphoric Acid Activated Babul Seed Carbon as an Adsorbent for the Removal of Methylene Blue

2008 ◽  
Vol 5 (4) ◽  
pp. 742-753 ◽  
Author(s):  
M. Sujatha ◽  
A. Geetha ◽  
P. Sivakumar ◽  
P. N. Palanisamy
Keyword(s):  
Methylene Blue ◽  
Activated Carbon ◽  
Adsorption Kinetics ◽  
Orthophosphoric Acid ◽  
Chemical Activation ◽  
Bet Surface Area ◽  
Isotherm Models ◽  
Blue Dye ◽  
Equilibrium Data ◽  
Pseudo Second Order

An Experimental and theoretical study has been conducted on the adsorption of methylene blue dye using activated carbon prepared from babul seed by chemical activation with orthophosphoric acid. BET surface area of the activated carbon was determined as 1060 m2/g. Adsorption kinetics, equilibrium and thermodynamics were investigated as a function of initial dye concentration, temperature and pH. First order Lagergren, pseudo-second order and Elovich kinetic models were used to test the adsorption kinetics. Results were analyzed by the Langmuir, Freundlich and Temkin isotherm models. Based on regression coefficient, the equilibrium data found fitted well to the Langmuir equilibrium model than other models. The characteristics of the prepared activated carbon were found comparable to the commercial activated carbon. It is found that the babul seed activated carbon is very effective for the removal of colouring matter.

Physical and Chemical Activation Effect on Activated Carbon Prepared from Local Pineapple Waste

2014 ◽  
Vol 699 ◽  
pp. 87-92 ◽  
Author(s):  
Abdul Rahim Yacob ◽  
Adlina Azmi ◽  
Mohd Khairul Asyraf Amat Mustajab
Keyword(s):  
Activated Carbon ◽  
Phosphoric Acid ◽  
Surface Area ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Bet Surface Area ◽  
Activation Effect ◽  
Pineapple Waste ◽  
Pineapple Peel ◽  
Physical And Chemical

The characteristics and quality of activated carbons prepared depending on the chemical and physical properties of the starting materials and the activation method used. In this study, activated carbon prepared using pineapple waste. Three parts of pineapple waste which comprises of peel, crown and leaf were studied. For comparison activated carbon were prepared by both physical and chemical activation respectively. Three types of chemicals were used, phosphoric acid (H3PO4), sulphuric acid (H2SO4), and potassium hydroxide (KOH). The preparation includes carbonization at 200°C and activation at the 400°C using muffle furnace. The chemical characterization of the activated carbon was carried out using Thermogravimetric analysis (TGA), Nitrogen gas adsorption analysis and Fourier transform infrared (FTIR). The highest BET surface area was achieved when the pineapple peel soaked in 20% phosphoric acid with a surface area of 1115 m2g-1. FTIR analysis indicates that the reacted pineapple waste successfully converted into activated carbons.

Sign in / Sign up

Export Citation Format

Share Document