scholarly journals Surface-Modified Biochar with Polydentate Binding Sites for the Removal of Cadmium

2019 ◽  
Vol 20 (7) ◽  
pp. 1775 ◽  
Author(s):  
Rongqi Chen ◽  
Xi Zhao ◽  
Juan Jiao ◽  
Yan Li ◽  
Min Wei

In this study, a surface chemical-modified rice husk biochar with abundant amino groups and disulfide bonds for the removal of cadmium was prepared using cystamine dihydrochloride as a modification ligand and glutaraldehyde as a crosslinker. The biochars were characterized by Fourier transform infrared spectrometry (FTIR), elemental analysis, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), thermogravimetry analysis (TGA), and nitrogen sorption (BET) before and after modification. The adsorption properties of the modified biochars for Cd (II) were investigated in detail via adsorption isotherm models, adsorption kinetics models, and selective adsorption experiments. The surfaces of the cystamine-modified biochars with granular nanopolymers of sufficient functional groups of primary amine and disulfide linkage rendered the biochar surface more conducive to electrostatic attraction and surface complexation. The theoretical maximum adsorption capacity of the modified biochars (81.02 mg g−1) was almost 10-fold greater than that of the raw biochars (8.347 mg g−1) for Cd (II). Besides, the cystamine-modified biochars had a better affinity for Cd (II) compared to other heavy metals (Zn, As, Cd, Co, Ni, Cr), showing six-fold greater affinity for Cd (II) than Zn2+. The results of this study indicate that the modification of biochars derived from rice husks shows great potential in the removal of Cd (II) from contaminated water.

Cellulose ◽  
2020 ◽  
Vol 27 (18) ◽  
pp. 10719-10732
Author(s):  
Janika Lehtonen ◽  
Jukka Hassinen ◽  
Avula Anil Kumar ◽  
Leena-Sisko Johansson ◽  
Roni Mäenpää ◽  
...  

AbstractWe investigate the adsorption of hexavalent uranium, U(VI), on phosphorylated cellulose nanofibers (PHO-CNF) and compare the results with those for native and TEMPO-oxidized nanocelluloses. Batch adsorption experiments in aqueous media show that PHO-CNF is highly efficient in removing U(VI) in the pH range between 3 and 6. Gelling of nanofiber hydrogels is observed at U(VI) concentration of 500 mg/L. Structural changes in the nanofiber network (scanning and transmission electron microscopies) and the surface chemical composition (X-ray photoelectron spectroscopy) gave insights on the mechanism of adsorption. The results from batch adsorption experiments are fitted to Langmuir, Freundlich, and Sips isotherm models, which indicate a maximum adsorption capacity of 1550 mg/g, the highest value reported so far for any bioadsorbent. Compared to other metals (Zn, Mn, and Cu) and typical ions present in natural aqueous matrices the phosphorylated nanofibers are shown to be remarkably selective to U(VI). The results suggest a solution for the capture of uranium, which is of interest given its health and toxic impacts when present in aqueous matrices.


2020 ◽  
Vol 81 (10) ◽  
pp. 2270-2280
Author(s):  
Yonggang Xu ◽  
Tianxia Bai ◽  
Yubo Yan ◽  
Yunfeng Zhao ◽  
Ling Yuan ◽  
...  

Abstract It is of great significance to remove Cr(VI) from water as a result of its high toxicity. Biochar from corn straw was modified by different acids (HNO3, H2SO4 and H3PO4) to remove Cr(VI) from aqueous solution. To estimate the removal mechanisms of Cr(VI) by the acid-modified biochars, batch experiments were performed in the light of contact time, Cr(VI) concentration, and pH, and the characteristics of acid-modified biochars before and after Cr(VI) adsorption were investigated by Fourier transform infrared spectra (FTIR) and X-ray photoelectron spectroscopy (XPS). The adsorption kinetics of Cr(VI) by acid-modified biochars were consistent with the pseudo-second-order model, and the adsorption isotherm obeyed the Freundlich model. Furthermore, the acid- modified biochars could supply more oxygen-containing functional groups (-COOH and -OH) as electron donor (e−) and hydrogen ion (H+) to enhance the reduction of Cr(VI) to Cr(III), resulting in enhanced removal of Cr(VI). HNO3-modified biochar exhibited the highest removal efficiency of Cr(VI). In general, the acid modifition of biochar was an effective method to increase the removal of Cr(VI).


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.


2016 ◽  
Vol 74 (7) ◽  
pp. 1644-1657 ◽  
Author(s):  
Mona El-Sayed ◽  
Gh. Eshaq ◽  
A. E. ElMetwally

In our study, Mg–Al–Zn mingled oxides were prepared by the co-precipitation method. The structure, composition, morphology and thermal stability of the synthesized Mg–Al–Zn mingled oxides were analyzed by powder X-ray diffraction, Fourier transform infrared spectrometry, N2 physisorption, scanning electron microscopy, differential scanning calorimetry and thermogravimetry. Batch experiments were performed to study the adsorption behavior of cobalt(II) and nickel(II) as a function of pH, contact time, initial metal ion concentration, and adsorbent dose. The maximum adsorption capacity of Mg–Al–Zn mingled oxides for cobalt and nickel metal ions was 116.7 mg g−1, and 70.4 mg g−1, respectively. The experimental data were analyzed using pseudo-first- and pseudo-second-order kinetic models in linear and nonlinear regression analysis. The kinetic studies showed that the adsorption process could be described by the pseudo-second-order kinetic model. Experimental equilibrium data were well represented by Langmuir and Freundlich isotherm models. Also, the maximum monolayer capacity, qmax, obtained was 113.8 mg g−1, and 79.4 mg g−1 for Co(II), and Ni(II), respectively. Our results showed that Mg–Al–Zn mingled oxides can be used as an efficient adsorbent material for removal of heavy metals from industrial wastewater samples.


2021 ◽  
Vol 1 (2) ◽  
pp. 98-107
Author(s):  
Zhi Hoong Ho ◽  
Liyana Amalina Adnan

Adsorption is one of the simplest techniques with low economic requirements. Coconut shell is an abundant agriculture waste which is inexpensive and easy to be obtained in Malaysia. This agriculture waste was transformed to activated carbon via 600°C of carbonization and zinc chloride activation. The ability of coconut shell-based activated carbon to remove phenolic compounds from aqueous solutions was evaluated. From the experiment, the equilibrium time for the adsorption of phenol onto coconut shell-based activated carbon is 120 minutes. The effect of the operating parameters, such as contact time, initial concentration, agitation speed, adsorbent dosage, and pH of the phenolic solution were studied. Adsorption kinetics models (pseudo-first-order, pseudo-second-order, and Elovich equation) and isotherm models (Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich) were used to fit the experimental data.Pseudo-second-order was found to be the best fitted kinetics model to describe the adsorption of phenol on coconut shell-based activated carbon. While the equilibrium experiment data was well expressed by the Temkin isotherm model, The maximum adsorption capacity is determined as 19.02 mg/g, which is comparatively lower than the previous research. Meanwhile, 92% of removal efficiency was achieved by a dosage of 10g/L. Meanwhile, the adsorption of phenol by activated carbon was more favorable under acidic conditions. The favourable isotherm behavior was indicated by the dimensionless separation factor. The functional group and compound class of activated carbon before and after the experiment were determined through the analysis of Fourier-transform infrared (FTIR) spectroscopy.


2018 ◽  
Vol 877 ◽  
pp. 26-32
Author(s):  
Bhargavi Gunturu ◽  
Geethalakshmi Ramakrishnan ◽  
Renganathan Sahadevan

Removal of a basic textile dye Methylene Blue from an aqueous solution was evaluated using biosorbent derived from Kigelia africana in a batch system. The influence of adsorption parameters such as adsorbent dosage (0.10-0.50g), PH (2-12) and initial dye concentration (0.3 to 0.11 g/L) on the adsorption process was studied. It was noticed that with increase in adsorbent dosage, the uptake capacity was decreased. Dye uptake was increased by changing the PH up to 8, further increase in PH caused reduced uptake. It was observed that, dye uptake by the adsorbent increased linearly with that of initial dye concentration. Equilibrium isotherm for the adsorption of methylene blue on to adsorbent was studied through Langmuir and Freundlich isotherm models. The data best fit with Freundlich model. Maximum adsorption capacity (Q ̊) was found to be 119.05mg/g. SEM and FTIR analyses of the adsorbent was performed before and after the adsorption, suggest that adsorption of the dye was through chemical interaction of the functional groups on the surface of the adsorbent. From the experimental results, it was inferred that biosorbent derived from Kigelia africana can be a potential alternate to activated carbon for textile dyes removal.


Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 962 ◽  
Author(s):  
Jifu Du ◽  
Zhen Dong ◽  
Yuxuan Pi ◽  
Xin Yang ◽  
Long Zhao

Two kinds of cotton linter-based adsorbents were synthesized by grafting dimethylaminoethyl methacrylate (DMAEMA) on cotton linter via radiation grafting polymerization, followed by further quaternization (QCL) or protonation (PCL). The effect of radiation dose and monomer concentration on grafting yield was optimized. The synthesized adsorbents were characterized by Fourier transform infrared spectrometry (FT-IR), Thermogravimetric Analysis (TGA), scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). The adsorption behaviors of the two adsorbents toward humic acid (HA) were investigated and discussed. pH effect studies showed that QCL was pH-independent, whereas PCL was just suitable for HA adsorption with pH < 6. The adsorption kinetics of the PCL and QCL adsorbent for HA removal were better described by pseudo-second-order kinetic mode and reached equilibrium in 40 min. The adsorption isotherms of the PCL and QCL adsorbent were well fitted with both Langmuir and Freundlich isotherm models, for which adsorption capacity reached 250 mg/g and 333 mg/g at pH 6, respectively. XPS analysis revealed the ratio of two amino group species at different pH, suggesting that the interaction mechanism of the adsorbent and HA was electrostatic adsorption.


2020 ◽  
Vol 18 (1) ◽  
pp. 1421-1432
Author(s):  
Zhaoqin Huang ◽  
Linchao Hu ◽  
Jingyu Dai

AbstractThe properties of rice husk biochar during the ageing process in soil and the resulting impacts on sorption capacity with respect to Cu(ii) were assessed. Rice husk-derived biochar was placed in fabric bags and buried in a plastic incubator filled with soil for 0–240 d. The aged biochar was then characterised and its sorption capacity compared with control (unaged) biochar in batch sorption experiments. The structural composition and morphology of the biochar before and after ageing were analysed based on element composition, scanning electron microscopy (SEM) coupled with energy X-ray dispersive spectroscopy (EDS), diffuse reflectance infrared Fourier transform infrared spectroscopy (DRIFTS), and X-ray photoelectron spectroscopy (XPS). The concentration of O, atomic O/C ratios, and carboxyl and hydroxyl functional groups increased at the surface of the biochar during ageing, which together indicated oxidation. Within the biochar particles, O/C ratios progressively increased towards their outer surfaces. Furthermore, ageing for more than 120 d facilitated Cu(ii) sorption as oxygen-containing groups were able to develop. The maximum adsorption capacity (qm) of biochar increased by 1.24 ∼ 1.32 times after ageing in the soil for 240 d. It is suggested that biochar surface properties were gradually altered during environmental exposure and the aged rice husk biochar showed increased performance in Cu(ii) adsorption. However, the performance of aged biochar as a soil remediator or conditioner will be affected by the ageing process and interactions among different soil components. As such, further research is required to evaluate these complex effects.


2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Muhammad Khairud Dahri ◽  
Muhammad Raziq Rahimi Kooh ◽  
Linda B. L. Lim

One of the major contaminants of water bodies is dye pollutants that come from textile, paper, and leather industries. In this study, Casuarina equisetifolia needle (CEN) is used to remove methyl violet 2B (MV) from aqueous solutions. Batch experiments were done to investigate the contact time, effect of pH, initial dye concentrations, and temperature. Langmuir and Freundlich isotherm models were used to describe the interaction between the adsorbate and adsorbent. The sorption mechanism was described using Lagergren 1st order, pseudo 2nd order, and Weber-Morris intraparticle diffusion models. FTIR spectroscopy was used to analyze the functional groups of CEN before and after sorption with MV. Optimal conditions were found to be at room temperature with 2 h contact time and no pH adjustment was needed. Experimental data was best fitted onto Langmuir model with maximum adsorption capacity of 164.99 mg/g, while pseudo 2nd order best described the experimental data for the kinetics study. Thermodynamic parameters such as change in Gibbs free energy (), enthalpy (), and entropy () were also investigated.


2017 ◽  
Vol 2017 ◽  
pp. 1-11
Author(s):  
Youxun Liu ◽  
Yaokun Wang ◽  
Mingyang Yan ◽  
Juan Huang

Hierarchical copper shells anchored on magnetic nanoparticles were designed and fabricated to selectively deplete hemoglobin from human blood by immobilized metal affinity chromatography. Briefly, CoFe2O4nanoparticles coated with polyacrylic acid were first synthesized by a one-pot solvothermal method. Hierarchical copper shells were then deposited by immobilizing Cu2+on nanoparticles and subsequently by reducing between the solid CoFe2O4@COOH and copper solution with NaBH4. The resulting nanoparticles were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectrometry, X-ray photoelectron spectroscopy, and vibrating sample magnetometry. The particles were also tested against purified bovine hemoglobin over a range of pH, contact time, and initial protein concentration. Hemoglobin adsorption followed pseudo-second-order kinetics and reached equilibrium in 90 min. Isothermal data also fit the Langmuir model well, with calculated maximum adsorption capacity 666 mg g−1. Due to the high density of Cu2+on the shell, the nanoparticles efficiently and selectively deplete hemoglobin from human blood. Taken together, the results demonstrate that the particles with hierarchical copper shells effectively remove abundant, histidine-rich proteins, such as hemoglobin from human blood, and thereby minimize interference in diagnostic and other assays.


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