scholarly journals Parametric Statistical Significance of Iron (II) Ions Adsorption by Coconut Shell in Aqueous Solutions

2019 ◽  
Vol 11 (1) ◽  
pp. 17-25
Author(s):  
Babatope Abimbola Olufemi ◽  
Anne Nlerum

The parametric statistical adsorption of chemically unmodified coconut shell powder (CSP) to adsorb iron (II) ions from aqueous solutions was examined in this work. It was observed that the adsorption capacity increased with increasing adsorbent dose, reducing adsorbate dose, increasing contact time, decreasing temperature and reducing particle size. As observed about one gram of the adsorbent was sufficient enough to remove 98 % iron (II) ions. A total contact time of about 40 minutes was sufficient for almost complete adsorption of the ions, while a pH of about 6.0 exhibited the maximum adsorption capacity. The sorption data were fitted into Langmuir, Freundlich, Temkin and the Dubinin-Radushkevich isotherms, fitted most with the Freundlich Isotherm model. The energy values obtained from the Temkin and Dubinin-Radushkevich isotherm model indicated high chemisorption phenomenon with the adsorbents. Investigation of some kinetic models confirmed that the adsorption of iron (II) ions using CSP was a pseudo-second order kinetic process, which further corroborates that chemisorption dominates the adsorption. Fourier Transform Analysis (FTIR) further established and justified the outcome of the study. The adsorption was parametrically justified statistically with Analysis of Variance (ANOVA) and Bonferroni-Holm Posthoc significance test. Conclusively, coconut shell proved strongly to be an effective and suitable adsorbent for removing iron (II) ions from aqueous solutions.

2017 ◽  
Vol 3 (1) ◽  
pp. 10 ◽  
Author(s):  
Saad A Alkahtani ◽  
Samer S Abu-Alrub ◽  
Ashraf M Mahmoud

<p>The adsorption behavior of Allura red (E129)<strong> </strong>from aqueous solutions onto activated carbon was successfully investigated. All factors affecting the adsorption process were carefully studied and the conditions were optimized. Adsorption of E129 onto activated carbon was found to increase by decreasing the mass of activated carbon, pH and ionic strength of the solution and by increasing temperature. The adsorption capacity of the activated carbon for Allura red was relatively high. Under the optimum conditions, the maximum adsorption capacity for E129 dye was 72.85 mg/g. Three adsorption models; Langmuir, Freundlich and Temkin model were investigated regarding the adsorption of E129. The models’ parameters K<sub>L</sub>, qm, R2, (n) were determined and found to be 0.0222, 72.85 mg/g, 0.9057-0.9984, and 0.992, respectively. Also, pseudo first and second-order kinetic models were tested to determine the best-fit model to the adsorption of E129 dye onto activated carbon. The results showed that the adsorption of E129 onto activated carbon obeyed both the Freundlich isotherm and pseudo second-order kinetic models. Moreover, thermodynamic studies indicated that the adsorption of E129 dye onto the activated carbon was spontaneous. </p>


2018 ◽  
Vol 1 (2) ◽  
pp. 30
Author(s):  
Saral Dwi Miftiyati ◽  
Saprini Hamdiani ◽  
Made Ganesh Darmayanti

A study has been conducted on the synthesis of paramagnetic mercapto silica hybrids as metal adsorbent of Ag(I). The aim of this study was to synthesis paramagnetic mercapto silica hybrid from rice husk ash waste, knowing the characteristics of paramagnetic mercapto silica hybrid from rice husk ash waste, and to determine the effect of pH, metal ions concentration, and the contact time on the value of adsorption capacity (Q). Based on the results of the study, it was found that paramagnetic mercapto silica hybrids can be synthesized from the rice husk ash waste. Characterization using FTIR spectroscopy showed that silanol (Si-OH), siloxan (Si-O-Si), -SH, and Fe-OH functional groups, and characterization of paramagnetic mercapto silica hybrid structures using XRD to show crystalline compounds with a position value of 2θ = 35.4 which showed that the magnetite material of Fe3O4 was coated by silica. Paramagnetic mercapto silica hybrids from rice husk waste can be used as adsorbent of Ag (I) metal at optimum conditions of pH 3, contact time of 120 minutes, and adsorption capacity of 392.01 mg/g. The suitable isotherm model is the Freundlich isotherm model which means the absorption of metal Ag (I) occurs physically, while adsorption of kinetics followed the pseudo II order kinetic model with a value of k  = 3.01 g.mg-1 minute-1.


2009 ◽  
Vol 620-622 ◽  
pp. 555-558
Author(s):  
Yi Li ◽  
Xue Gang Luo ◽  
Zhao Liu ◽  
Yan Huang ◽  
Xiao Yan Long

The modified valonian tannin was prepared through sulfonated-mannich reaction and used to adsorb Cu (II) from the aqueous solutions. The adsorption capacity rapidly reached equilibrium within 2 hours. The effect of pH on adsorption was apparent, the amount of adsorption increased significantly as the pH increased from 2.0 to 4.0 and then leveled off at pH 4.0-6.0. Equilibrium data fitted well with Freundlich isotherm model compared to Langmuir isotherm model, indicating that adsorption takes place on heterogeneous surface of the modified valonia tannin. The adsorption capacity was increased by increasing initial concentrations. The maximum adsorption capacity of cooper ion was determined to be 56.200 mg/g at 100 mg/L concentration.


Materials ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 942 ◽  
Author(s):  
Huo-Xi Jin ◽  
Hong Xu ◽  
Nan Wang ◽  
Li-Ye Yang ◽  
Yang-Guang Wang ◽  
...  

The ability to remove toxic heavy metals, such as Pb(II), from the environment is an important objective from both human-health and ecological perspectives. Herein, we describe the fabrication of a novel carboxymethylcellulose-coated metal organic material (MOF-5–CMC) adsorbent that removed lead ions from aqueous solutions. The adsorption material was characterized by Fourier-transform infrared spectroscopy, X-ray diffractometry, scanning electron microscopy, and X-ray photoelectron spectroscopy. We studied the functions of the contact time, pH, the original concentration of the Pb(II) solution, and adsorption temperature on adsorption capacity. MOF-5–CMC beads exhibit good adsorption performance; the maximum adsorption capacity obtained from the Langmuir isotherm-model is 322.58 mg/g, and the adsorption equilibrium was reached in 120 min at a concentration of 300 mg/L. The adsorption kinetics is well described by pseudo-second-order kinetics, and the adsorption equilibrium data are well fitted to the Langmuir isotherm model (R2 = 0.988). Thermodynamics experiments indicate that the adsorption process is both spontaneous and endothermic. In addition, the adsorbent is reusable. We conclude that MOF-5–CMC is a good adsorbent that can be used to remove Pb(II) from aqueous solutions.


2010 ◽  
Vol 5 (1) ◽  
Author(s):  
Hülya Karaca ◽  
Turgay Tay ◽  
Merih Kıvanç

The biosorption of lead ions (Pb2+) onto lyophilized fungus Aspergillus niveus was investigated in aqueous solutions in a batch system with respect to pH, contact time and initial concentration of the ions at 30 °C. The maximum adsorption capacity of lyophilized A. niveus was found to be 92.6 mg g−1 at pH 5.1 and the biosorption equilibrium was established about in 30 min. The adsorption capacity obtained is one of the highest value among those reported in the literature. The kinetic data were analyzed using the pseudo-first-order kinetic, pseudo-second-order kinetic, and intraparticle diffusion equations. Kinetic parameters, such as rate constants, equilibrium adsorption capacities, and related correlation coefficients for the kinetic models were calculated and discussed. It was found that the adsorption of lead ions onto lyophilized A. niveus biomass fit the pseudo-second-order kinetic model well. The Langmuir and Freundlich isotherm parameters for the lead ion adsorption were applied and the Langmuir model agreed better with the adsorption of lead ions onto lyophilized A. niveus.


2020 ◽  
Vol 10 (5) ◽  
pp. 1738
Author(s):  
Kay Thwe Aung ◽  
Seung-Hee Hong ◽  
Seong-Jik Park ◽  
Chang-Gu Lee

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.


2020 ◽  
Vol 38 (7-8) ◽  
pp. 254-270
Author(s):  
Yuanrong Zhu ◽  
Xianming Yue ◽  
Fazhi Xie

Reducing input of phosphorus is the key step for control of eutrophication and algal blooming in freshwater lakes. Adsorption technology is a cost-effective technology for phosphate removal in water for the purpose. Thus, in this study, a novel Fe–Mn–La tri-metal composite sorbent was developed, and then evaluated for phosphate removal. The results showed that the maximum adsorption capacity could be approached to 61.80 mg g−1 at 25°C under pH of 6.03. Adsorption of phosphate by Fe–Mn–La tri-metal composite adsorbent fitted better by pseudo-second-order kinetic equation and Langmuir model, which suggested that the adsorption process was surface chemical reactions and mainly in a monolayer coverage manner. The thermodynamic study indicated that the adsorption reaction was an endothermic process. The phosphate removal gradually decreased with the increasing of pH from 3.02 to 11.00. The sequence of coexisting anions competing with phosphates was that CO32− > Cl− > SO42− > NO3−. Dissolved organic matter, fulvic acid as a representative, would also decrease adsorption capacities of phosphate by Fe–Mn–La tri-metal composite adsorbents. Adsorption capacity would be decreased with increasing addition of adsorbents, while removal efficiency would be increased in this process. The Fe–Mn–La tri-metal composite adsorbent showed a good reusability when applied to removal of dissolved phosphate from aqueous solutions. The Fourier transform infrared spectrometer and X-ray photoelectron spectroscopy analyses indicated that some hydroxyl groups (–OH) on the surface of adsorbent were replaced by the adsorbed PO43−, HPO42−, or H2PO4−. Aggregative results showed that the novel Fe–Mn–La tri-mental composite sorbent is a very promising adsorbent for the removal of phosphate from aqueous solutions.


2018 ◽  
Vol 5 (5) ◽  
pp. 172382 ◽  
Author(s):  
Wei Guo ◽  
Shujuan Wang ◽  
Yunkai Wang ◽  
Shaoyong Lu ◽  
Yue Gao

A magnetically modified rice husk biochar (MBC) was successfully prepared by a hydrothermal method from original biochar (BC) and subsequently used to remove phenanthrene (PHE) from aqueous solutions. The porosity, specific surface area and hydrophobicity of BC were significantly improved (approx. two times) after magnetic modification. The adsorption data fitted well to pseudo-second-order kinetic and Langmuir models. Compared with BC, MBC had a faster adsorption rate and higher adsorption capacity of PHE. The adsorption equilibrium for PHE on MBC was achieved within 1.0 h. The maximum adsorption capacity of PHE on MBC was 97.6 mg g −1 based on the analysis of the Sips model, which was significantly higher than that of other sources of BCs. The adsorption mechanism of the two BCs was mainly attributed to the action of surface functional groups and π–π-conjugated reactions. The adsorption of PHE on MBC mainly occurred in the functional groups of C–O and Fe 3 O 4 , but that on BC was mainly in the functional groups of –OH, N–H, C=C and C–O.


2021 ◽  
Author(s):  
Mingyue Piao ◽  
Hongxue Du ◽  
Yuwei Sun ◽  
Honghui Teng

Abstract Hybrid hydrogel was synthesized by immobilizing TiO2 in polyethylene glycol diacrylate (TiO2@PEGDA) as an efficient adsorbent with photocatalysis property for bisphenol A (BPA) elimination. TiO2@PEGDA exhibited spherical and rough structure with limited crystallinity and abundant functional groups. The contact angle was 61.96°, indicating that TiO2@PEGDA is hydrophilic. The swelling capacity of TiO2@PEGDA (9.0%) was decreased compared with pristine PEGDA (15.6%). Adsorption results demonstrated that the maximum adsorption capacity of TiO2@PEGDA (101.4 mg/g) for BPA was slightly higher than pristine PEGDA (97.68 mg/g). The adsorption capacity was independent with pH at pH < 8.0, and decreased obviously when the value of pH was higher than 8.0. The adsorption behavior was fitted well with the pseudo-second-order kinetic and the Freundlich isotherm model. Both ΔG0 and ΔH0 were negative, indicating that BPA adsorbed on TiO2@PEGDA was an exothermic and spontaneous process. Regeneration study was performed by photocatalysis, and the adsorption capacity was 85.6% compared with the initial capacity after four cycles of illumination, indicating that TiO2@PEGDA could be recycled without significant loss of adsorption capacity. Consequently, TiO2@PEGDA can serve as an eco-friendly and promising material for efficiently adsorbing BPA with self-clean property.


Polymers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 3054
Author(s):  
Yiming Zhou ◽  
Te Li ◽  
Juanli Shen ◽  
Yu Meng ◽  
Shuhua Tong ◽  
...  

This article reports effective removal of methylene blue (MB) dyes from aqueous solutions using a novel magnetic polymer nanocomposite. The core-shell structured nanosorbents was fabricated via coating Fe3O4 nanoparticles with a layer of hydrogel material, that synthesized by carboxymethyl cellulose cross-linked with poly(acrylic acid-co-acrylamide). Some physico-chemical properties of the nanosorbents were characterized by various testing methods. The nanosorbent could be easily separated from aqueous solutions by an external magnetic field and the mass fraction of outer hydrogel shell was 20.3 wt%. The adsorption performance was investigated as the effects of solution pH, adsorbent content, initial dye concentration, and contact time. The maximum adsorption capacity was obtained at neutral pH of 7 with a sorbent dose of 1.5 g L−1. The experimental data of MB adsorption were fit to Langmuir isotherm model and Pseudo-second-order kinetic model with maximum adsorption of 34.3 mg g−1. XPS technique was applied to study the mechanism of adsorption, electrostatic attraction and physically adsorption may control the adsorption behavior of the composite nanosorbents. In addition, a good reusability of 83.5% MB recovering with adsorption capacity decreasing by 16.5% over five cycles of sorption/desorption was observed.


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