Phosphonium grafted styrene–divinylbenzene resins impregnated with iron(III) and crown ethers for arsenic removal

2014 ◽  
Vol 86 (11) ◽  
pp. 1729-1740 ◽  
Author(s):  
Adina Negrea ◽  
Adriana Popa ◽  
Mihaela Ciopec ◽  
Lavinia Lupa ◽  
Petru Negrea ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Arsenic Removal ◽  
Arsenic Concentration ◽  
Underground Water ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Iron Ions ◽  
Arsenic Adsorption ◽  
Equilibrium Data ◽  
Styrene Divinylbenzene

Abstract In the present work a polymer with phosphonium pendant groups impregnated with crown ether (dibenzo-18-crown-6) and loaded with iron ions was investigated for arsenic removal through adsorption from aqueous solutions. The impregnated polymer was loaded with iron ions due to the high affinity of arsenic to it. The characterization of the surface modification of the obtained new adsorbent material was performed on the basis of energy dispersive X-ray analysis; scanning electron microscopy and Fourier transform infrared spectroscopy. The arsenic adsorption was investigated, including effect of pH, arsenic initial concentration, the shaking time and temperature. The effect of the pH was examined over the range 2–11. The adsorption of As(V) increases with pH increasing reaching a maximum at pH higher than 8. Equilibrium, kinetic and thermodynamic studies were carried out to study the adsorption performance of the obtained material in the removal process of arsenic from aqueous solutions. For the studied materials the equilibrium data closely fitted Langmuir model and was achieved a maximum adsorption capacity of 32.6 μg As(V)/g of material. The pseudo-second order kinetic model is suitable for describing the adsorption system. The obtained results show that the studied adsorbent can be used with efficiency in the arsenic removal from underground water even from low influent arsenic concentration solutions.

Alkaline deoxygenated graphene oxide as adsorbent for cadmium ions removal from aqueous solutions

2015 ◽  
Vol 71 (11) ◽  
pp. 1611-1619 ◽  
Author(s):  
Jun Liu ◽  
Hongyan Du ◽  
Shaowei Yuan ◽  
Wanxia He ◽  
Pengju Yan ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Aqueous Solutions ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Transmission Electron ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ft Ir

Alkaline deoxygenated graphene oxide (aGO) was prepared through alkaline hydrothermal treatment and used as adsorbent to remove Cd(II) ions from aqueous solutions for the first time. The characterization results of transmission electron microscopy, X-ray diffraction, Raman spectroscopy, and Fourier transform infrared (FT-IR) spectra indicate that aGO was successfully synthesized. The batch adsorption experiments showed that the adsorption kinetics could be described by the pseudo-second-order kinetic model, and the isotherms equilibrium data were well fitted with the Langmuir model. The maximum adsorption capacity of Cd(II) on aGO was 156 mg/g at pH 5 and T = 293 K. The adsorption thermodynamic parameters indicated that the adsorption process was a spontaneous and endothermic reaction. The mainly adsorption mechanism speculated from FT-IR results may be attributed to the electrostatic attraction between Cd2+ and negatively charged groups (–CO−) of aGO and cation-π interaction between Cd2+ and the graphene planes. The findings of this study demonstrate the potential utility of the nanomaterial aGO as an effective adsorbent for Cd(II) removal from aqueous solutions.

scholarly journals Enhanced As(III) sequestration using nanoscale zero-valent iron modified by combination of loading and sulfidation: characterizations, performance, kinetics and mechanism

2021 ◽  
Author(s):  
Shun Cheng ◽  
Hong Liu ◽  
Emmanuella Anang ◽  
Chunxia Li ◽  
Xianyuan Fan
Keyword(s):  
Arsenic Removal ◽  
Average Particle Size ◽  
Zero Valent Iron ◽  
Maximum Adsorption Capacity ◽  
Average Particle ◽  
Order Kinetic ◽  
Arsenic Adsorption ◽  
Nanoscale Zero Valent Iron ◽  
Wide Ph Range ◽  
Co Precipitation

Abstract Nanoscale zero-valent iron (nZVI) and sulfides have been confirmed to be effective in arsenic sequestration from aqueous solution. In this study, attapulgite supported and sulfide-modified nanoscale zero-valent iron (S-nZVI@ATP) are synthesized to realize the superposition effect of enhanced arsenic sequestration. The results indicated that nZVI clusters were well disaggregated and the BET specific surface area increased from 19.61 m2·g−1 to 46.04 m2·g−1 of S-nZVI@ATP, resulting in an enhanced removal efficiency of arsenic from 51.4% to 65.1% at 20 min. The sulfides in S-nZVI@ATP mainly exists as mackinawite (FeS) and causes the spherical nanoparticles exhibiting a larger average particle size (94.6 nm) compared to bare nZVI (66.0 nm). In addition, S-nZVI@ATP exhibited a prominent ability for arsenic sequestration over a wide pH range of 3.0–6.0. The presence of anions SO42− and Cl− can enhance the arsenic removal whereas HCO3− inhibited it. The arsenic adsorption by S-nZVI@ATP could be explained by the pseudo-second-order kinetic model and the Langmuir model, with the maximum adsorption capacity of 193.8 mg·g−1. The mechanism of As(III) sequestration by S-nZVI@ATP involved multiple processes, mainly including precipitation conversion from FeS to As2S3, surface-complexation adsorption and co-precipitation.

Sulfonic Acid Functionalized Magnetite Nanoporous-KIT-6 for Removal of Methyl Green from Aqueous Solutions

2018 ◽  
Vol 52 ◽  
pp. 54-70 ◽  
Author(s):  
Seyedeh Mahsa Seyed Danesh ◽  
Hossein Faghihian ◽  
Shahab Shariati
Keyword(s):  
Aqueous Solutions ◽  
Sulfonic Acid ◽  
Mesoporous Silica Nanoparticles ◽  
Freundlich Isotherm ◽  
Maximum Adsorption Capacity ◽  
Methyl Green ◽  
Order Kinetic ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Wastewater Samples

The sulfonic acid-functionalized KIT-6 magnetite mesoporous silica nanoparticles (Fe3O4@SiO2@KIT-6-SO3H NPs) were prepared as an adsorbent and used for the removal of methyl green from aqueous solutions. Characterization of the obtained adsorbent was done by FT-IR, SEM and EDX instruments. According to the experimental results, about 96.4 % of dye was removed from aqueous solutions at the adsorbent amount of 3.2 g L-1at pH = 3 and ionic strength = 0 during 10 min. The kinetic results indicated that the pseudo-second-order kinetic model was the best model for describing the adsorption kinetic ( = 0.9999). The isotherm analysis demonstrated that the equilibrium data were well fitted to the Freundlich isotherm model, showing a multilayer adsorption of the dye on the adsorbent surface. The maximum adsorption capacity for methyl green was obtained 196 mg g-1. Furthermore, the Fe3O4@SiO2-KIT-6-SO3H NPs could be simply recovered by external magnet and it exhibited recyclability and reusability for six cycles. The results showed that the Fe3O4@SiO2-KIT-6-SO3H NPs are appropriate adsorbent for removal of methyl green from real wastewater samples.

As(III) Removal by Dynamic Adsorption onto Amberlite XAD7 Functionalized with Crown Ether and Doped with Fe(III) Ions

2019 ◽  
Vol 70 (7) ◽  
pp. 2330-2334
Author(s):  
Mihaela Ciopec ◽  
Adina Negrea ◽  
Narcis Duteanu ◽  
Corneliu Mircea Davidescu ◽  
Iosif Hulka ◽  
...  
Keyword(s):  
Adsorption Process ◽  
Arsenic Removal ◽  
Arsenic Concentration ◽  
Fixed Bed ◽  
World Health ◽  
Arsenic Content ◽  
Arsenic Adsorption ◽  
Stage Of Development ◽  
Wide Range ◽  
Health Organization

Arsenic content in groundwater�s present a wide range of concentration, ranging from hundreds of micrograms to thousands of micrograms of arsenic per litter, while the maximum permitted arsenic concentration established by World Health Organization (WHO) is 10 mg L-1. According to the WHO all people, regardless of their stage of development and their social economic condition, have the right to have access to adequate drinking water. The most efficient and economic technique used for arsenic removal is represented by adsorption. In order to make this remediation technique more affordable and environmentally friendly is important to new materials with advance adsorbent properties. Novelty of present paper is represented by the usage of a new adsorbent material obtained by physical - chemical modification of Amberlite XAD polymers using crown ethers followed by iron doping, due to well-known affinity of arsenic for iron ions. Present paper aims to test the obtained modified Amberlite polymer for arsenic removal from real groundwater by using adsorption in a fixed bed column, establishing in this way a mechanism for the adsorption process. During experimental work was studied the influence of competing ions from real water into the arsenic adsorption process.

Comparison of the fixation of several metal ions onto a low-cost biopolymer

2002 ◽  
Vol 2 (5-6) ◽  
pp. 217-224 ◽  
Author(s):  
Z. Reddad ◽  
C. Gérente ◽  
Y. Andrès ◽  
P. Le Cloirec
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Low Cost ◽  
Operating Conditions ◽  
Order Kinetic ◽  
Adsorption Mechanisms ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Beet Pulp ◽  
Removal Of Metal Ions

In the present work, sugar beet pulp, a common waste from the sugar refining industry, was studied in the removal of metal ions from aqueous solutions. The ability of this cheap biopolymer to sorb several metals namely Pb2+, Cu2+, Zn2+, Cd2+ and Ni2+ in aqueous solutions was investigated. The metal fixation capacities of the sorbent were determined according to operating conditions and the fixation mechanisms were identified. The biopolymer has shown high elimination rates and interesting metal fixation capacities. A pseudo-second-order kinetic model was tested to investigate the adsorption mechanisms. The kinetic parameters of the model were calculated and discussed. For 8 × 10-4 M initial metal concentration, the initial sorption rates (v0) ranged from 0.063 mmol.g-1.min-1 for Pb2+ to 0.275 mmol.g-1.min-1 for Ni2+ ions, with the order: Ni2+ > Cd2+ > Zn2+ > Cu2+ > Pb2+. The equilibrium data fitted well with the Langmuir model and showed the following affinity order of the material: Pb2+ > Cu2+ > Zn2+ > Cd2+ > Ni2+. Then, the kinetic and equilibrium parameters calculated qm and v0 were tentatively correlated to the properties of the metals. Finally, equilibrium experiments in multimetallic systems were performed to study the competition of the fixation of Pb2+, Zn2+ and Ni2+ cations. In all cases, the metal fixation onto the biopolymer was found to be favourable in multicomponent systems. Based on these results, it is demonstrated that this biosorbent represents a low-cost solution for the treatment of metal-polluted wastewaters.

scholarly journals Evaluation of Fe-Mg Binary Oxide for As (III) Adsorption—Synthesis, Characterization and Kinetic Modelling

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 805
Author(s):  
Saif Ullah Khan ◽  
Rumman Zaidi ◽  
Feroz Shaik ◽  
Izharul Haq Farooqi ◽  
Ameer Azam ◽  
...  
Keyword(s):  
Arsenic Removal ◽  
Kinetic Modelling ◽  
Arsenic Concentration ◽  
Experimental Studies ◽  
Precipitation Method ◽  
Arsenic Adsorption ◽  
Adsorbent Dosage ◽  
X Ray ◽  
Co Precipitation ◽  
Contaminated Waters

Nanotechnology has received much attention in treating contaminated waters. In the present study, a facile co-precipitation method was employed to synthesize a novel iron and magnesium based binary metal oxide using a stoichiometrically fixed amount of FeNO3.9H2O and MgNO3.6H2O in a proportion of molar concentration 1:1 and was later evaluated in removing As (III) from contaminated waters. Characterization of the prepared nanomaterial was done using X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy Dispersive X-Ray Analysis (EDAX) and ultraviolet–visible spectrophotometry (UV-VIS). Experimental studies on batch scale were carried out, examining the effect of varying initial concentrations of metal, adsorbent dosage, application time and initial pH on removal efficiency. Arsenic removal increased on increasing adsorbent dosage (0.1–1 g/L) but trend reversed on increasing initial arsenic concentration attaining qmax of 263.20 mg/g. Adsorption was quite efficient in pH range 4–8. Freundlich fitted better for adsorption isotherm along with following Pseudo-2nd order kinetics. The reusability and effect of co-existing ions on arsenic adsorption, namely SO42−, CO32− and PO43− were also explored with reusability in 1st and 2nd cycles attained adsorptive removal up to 77% and 64% respectively. The prepared nano-adsorbent showed promising results in terms of high arsenic uptake (qmax of 263.20 mg/g) along with facile and cost-effective synthesis. Thus, the co-precipitation technique used in this work is a simple one step procedure without any use of any precursor as compared to most of the other procedures used for synthesis.

scholarly journals Synthesis characterization and sorption properties of a sorbent synthesized using slag and red mud: Arsenic removal from spiked aqueous solutions

2016 ◽  
Vol 18 (2) ◽  
pp. 339-347 ◽  
Keyword(s):  
Aqueous Solutions ◽  
Red Mud ◽  
Arsenic Removal ◽  
Point Of Zero Charge ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
Equilibrium Studies ◽  
Metallurgical Wastes ◽  
Bet Method ◽  
Gf Aas

<p>The aim of the present study was to synthesize a sorbent, for arsenic removal from aqueous solutions, reusing two waste materials (slag and red mud). The sorbent was prepared after chemical and thermal treatment, during which amorphous silica sol and FeOOH sol were produced simultaneously and form Fe-Si complexes on the surface of the slag. To characterize the sorbent Powder X-ray diffraction (XRD); Fourier transform infrared (FTIR) spectroscopy and Scanning Electron Microscopy (SEM-EDX) were applied. The surface area (BET method) and the Point of Zero Charge (PZC) of the sorbent were determined.). The sorption efficiency of the sorbent produced was investigated with kinetic and equilibrium studies, performed in batch conditions. The concentration of arsenic in solutions was determined by electro thermal atomic absorption spectroscopy (GF-AAS). The results of the study showed that with the described process, using metallurgical wastes, iron oxyhydroxides were &ldquo;loaded&rdquo; onto slag producing an effective sorbent for arsenic removal. Kinetic experiments proved that equilibrium was achieved within 15 hours, while the maximum adsorption capacity as evidenced by equilibrium experiments, was 16.14 mg g<sup>-1</sup>. Data proved to fit better to the Langmuir equation.</p>

scholarly journals Utilization to Remove Pb (II) Ions from Aqueous Environments Using Waste Fish Bones by Ion Exchange

2014 ◽  
Vol 2014 ◽  
pp. 1-12 ◽  
Author(s):  
Bayram Kizilkaya ◽  
A. Adem Tekınay
Keyword(s):  
Aqueous Solutions ◽  
Adsorption Mechanism ◽  
Cost Effective ◽  
Isotherm Models ◽  
Maximum Adsorption Capacity ◽  
Fish Bones ◽  
Adsorption Capacities ◽  
Aqueous Environments ◽  
Equilibrium Data ◽  
Pseudo Second Order

Removal of lead (II) from aqueous solutions was studied by using pretreated fish bones as natural, cost-effective, waste sorbents. The effect of pH, contact time, temperature, and metal concentration on the adsorption capacities of the adsorbent was investigated. The maximum adsorption capacity for Pb (II) was found to be 323 mg/g at optimum conditions. The experiments showed that when pH increased, an increase in the adsorbed amount of metal of the fish bones was observed. The kinetic results of adsorption obeyed a pseudo second-order model. Freundlich and Langmuir isotherm models were applied to experimental equilibrium data of Pb (II) adsorption and the value ofRLfor Pb (II) was found to be 0.906. The thermodynamic parameters related to the adsorption process such asEa,ΔG°,ΔH°, andΔS° were calculated andEa,ΔH°, andΔS° were found to be 7.06, 46.01 kJ mol−1, and 0.141 kJ mol−1K−1for Pb (III), respectively.ΔH° values (46.01 kJmol−1) showed that the adsorption mechanism was endothermic. Weber-Morris and Urano-Tachikawa diffusion models were also applied to the experimental equilibrium data. The fish bones were effectively used as sorbent for the removal of Pb (II) ions from aqueous solutions.

scholarly journals Removal of Cu(II) from Aqueous Solutions Using Amine-Doped Polyacrylonitrile Fibers

2020 ◽  
Vol 10 (5) ◽  
pp. 1738
Author(s):  
Kay Thwe Aung ◽  
Seung-Hee Hong ◽  
Seong-Jik Park ◽  
Chang-Gu Lee
Keyword(s):  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Isotherm Models ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Equilibrium Studies ◽  
Naoh Solution ◽  
Surface Modified ◽  
Pan Fibers

Polyacrylonitrile (PAN) fibers were prepared via electrospinning and were modified with diethylenetriamine (DETA) to fabricate surface-modified PAN fibers. The surface-modified PAN fibers were used to evaluate their adsorption capacity for the removal of Cu(II) from aqueous solutions. Batch adsorption experiments were performed to examine the effects of the modification process, initial concentration, initial pH, and adsorbent dose on the adsorption of Cu(II). Kinetic analysis revealed that the experimental data fitted the pseudo-second-order kinetic model better than the pseudo-first-order model. Adsorption equilibrium studies were conducted using the Freundlich and Langmuir isotherm models, and the findings indicated that the PAN fibers modified with 85% DETA presented the highest adsorption capacity for Cu(II) of all analyzed samples. Moreover, the results revealed that the Freundlich model was more appropriate than the Langmuir one for describing the adsorption of Cu(II) onto the modified fibers at various initial Cu(II) concentrations. The maximum adsorption capacity was determined to be 87.77 mg/g at pH 4, and the percent removal of Cu(II) increased as the amount of adsorbent increased. Furthermore, the surface-modified PAN fibers could be easily regenerated using NaOH solution. Therefore, surface-modified PAN fibers could be used as adsorbents for the removal of Cu(II) from aqueous solutions.

Preparation of Graphene Oxide Modified Rice Husk for Cr(VI) Removal

2019 ◽  
Vol 19 (11) ◽  
pp. 7035-7043 ◽  
Author(s):  
Tong Ouyang ◽  
Jidan Tang ◽  
Fang Liu ◽  
Chang-Tang Chang
Keyword(s):  
Graphene Oxide ◽  
Adsorption Capacity ◽  
Rice Husk ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Adsorption Sites ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Alkaline Conditions ◽  
Rice Husk Biochar

The objective of this paper is to study the removal of Cr(VI) in aqueous solution by using a new graphene oxide-coated rice husk biochar composite (GO-RHB). GO-RHB is a synthetic material having a porous structure with lots of oxygen-containing functional groups and a large surface area that provide effective adsorption sites. Experiments showed that GO-RHB had higher adsorption capacity under acidic than under alkaline conditions. At pH of 2, GO-RHB has the maximum adsorption capacity(48.8 mg g−1). Equilibrium data obtained by fitting with the Langmuir and Freundlich models indicate that the reaction process was monolayer adsorption. The adsorption of Cr(VI) followed the pseudo-second-order kinetic model that illustrates chemical adsorption. Intraparticlediffusion studies further revealed that film diffusion was taking place. Moreover, the results of thermodynamics showed that the adsorption process was endothermic and spontaneous in nature. The removal mechanism of Cr(VI) was also explained in detail. The prepared adsorbent is highly efficient and might be useful than many other conventional adsorbent used for the removal of Cr(VI) from wastewater.

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