Removal of Hg(II) from aqueous solution using sodium humate as heavy metal capturing agent

2016 ◽  
Vol 74 (12) ◽  
pp. 2946-2957 ◽  
Author(s):  
Shixiang Wang ◽  
Yong Liu ◽  
Qin Fan ◽  
Anlan Zhou ◽  
Lu Fan ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
X Ray ◽  
Sodium Humate ◽  
Initial Ph ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
The Fourier Transform ◽  
Hydroxy Groups ◽  
Reaction Equilibrium ◽  
Coordination Reaction

An environmental friendly and economic natural biopolymer-sodium humate (HA-Na) was used to capture Hg(II) from aqueous solutions, and the trapped Hg(II) (HA-Na-Hg) was then removed by aluminium coagulation. The best Hg(II) capturing performance (90.60%) was observed under the following conditions: initial pH of 7.0, coagulation pH of 6.0, HA-Na dosage of 5.0 g L−1, Al2(SO4)3.18H2O dosage of 4.0 g L−1, initial Hg(II) concentration of 50 mg L−1 and capturing time of 30 min. The HA-Na compositions with the molecular weight beyond 70 kDa showed the most intense affinity toward Hg(II). The results showed that the reaction equilibrium was achieved within 10 min (pH 7.0), and could be well fitted by the pseudo-second-order kinetics model. The capturing process could be well described by the Langmuir isotherm model and the maximum capturing capacity of Hg(II) was high up to 9.80 mg g−1 at 298 K (pH 7.0). The Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) analysis showed that the redox reaction between Hg(II) and HA-Na and the coordination reaction of carboxyl and hydroxy groups of HA-Na with Hg(II) were responsible for Hg(II) removal. The successive regeneration experiment showed that the capturing efficiency of humates for Hg(II) was maintained at about 51% after five capture-regeneration recycles.

scholarly journals Adsorption of Lead (II) from Aqueous Solution with High Efficiency by Hydrothermal Biochar Derived from Honey

2020 ◽  
Vol 17 (10) ◽  
pp. 3441 ◽  
Author(s):  
Bo Wang ◽  
Jie Yu ◽  
Hui Liao ◽  
Wenkun Zhu ◽  
Pingping Ding ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
High Efficiency ◽  
Raw Material ◽  
Before And After ◽  
Initial Ph ◽  
Carboxylic Groups ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Natural Honey

A novel natural honey hydrothermal biochar (HHTB) was prepared using natural honey as raw material. The as-prepared adsorbent was applied to adsorb Pb2+ from aqueous solution and characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy to investigate the structure and morphology change of the adsorbent before and after Pb2+ adsorption. The influence of the pH, initial Pb2+ concentration, temperature, and contact time on the adsorption of Pb2+ was systematically investigated. The results revealed that the adsorption capacity for Pb2+ is up to 133.2 mg·g−1 at initial pH of 5.0 and adsorption temperature of 298 K. Meanwhile, the adsorption of Pb2+ on HHTB can be well fitted by the pseudo-second-order model and Langmuir isotherm model. The adsorbent had great selectivity for Pb2+ from the aqueous solution containing coexisting ions including Cd2+, Co2+, Cr3+, Cu2+, Ni2+ and Zn2+. Furthermore, the adsorption of Pb2+ on HHTB was attributed to complexation coordination, where it involved hydroxyl and carboxylic groups on HHTB in the process of adsorption of Pb2+.

scholarly journals Green Synthesis of A Novel MXene–CS Composite Applied in Treatment of Cr(VI) Contaminated Aqueous Solution

Processes ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 524
Author(s):  
Hongyou Wan ◽  
Lan Nan ◽  
Huikai Geng ◽  
Wei Zhang ◽  
Huanhuan Shi
Keyword(s):  
Photoelectron Spectroscopy ◽  
Environmental Concern ◽  
Maximum Adsorption Capacity ◽  
Aqueous Environment ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Xrd Patterns

The considerable amount of Cr(VI) pollutants in the aqueous environment is a significant environmental concern that cannot be ignored. A series of novel Mxene–CS inorganic–organic composite nanomaterials synthesized by using the solution reaction method was applied to treat the Cr(VI) contaminated water. The Mxene–CS composites were characterized through SEM (scanning electron microscope), XRD (X–ray diffraction), XPS (X–ray photoelectron spectroscopy), and FTIR (Fourier transform infrared). The XRD patterns (observed at 2θ of 18.1°, 35.8°, 41.5°, and 60.1°) and the FT–IR spectra (-NH2 group for 1635 and 1517 cm−1, and -OH group for 3482 cm−1) illustrated that CS was successfully loaded on the Mxene. The effects of solution pH, the dosage of Mxene–CS, and duration time on the adsorption of Cr(VI) by synthesized Mxene–CS were investigated. The removal efficiency of Cr(VI) was increased from 12.9% to 40.5% with Mxene–CS dosage ranging from 0.02 to 0.12 g/L. The adsorption process could be well fitted by the pseudo–second–order kinetics model, indicating chemisorption occurred. The Langmuir isotherm model could be better to describe the process with a maximum adsorption capacity of 43.1 mg/g. The prepared novel Mxene–CS composite was considered as an alternative for adsorption of heavy metals from wastewater.

scholarly journals Tannin-based biosorbent encapsulated into calcium alginate beads for Cr(VI) removal

2020 ◽  
Vol 81 (5) ◽  
pp. 936-948 ◽  
Author(s):  
Xubing Sun ◽  
Jiayong Zhang ◽  
Guowen Ding ◽  
Yaohui You
Keyword(s):  
Photoelectron Spectroscopy ◽  
Calcium Alginate ◽  
Alginate Beads ◽  
Formaldehyde Resin ◽  
X Ray Diffraction ◽  
X Ray ◽  
Intra Particle Diffusion ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Low Toxicity

Abstract A composite biosorbent (AC-TFR) prepared by encapsulating tannin-formaldehyde resin (TFR) into calcium alginate (AC) beads was used to remove Cr(VI) from an aqueous solution. Various influencing factors, such as TFR dosage, pH, initial Cr(VI) concentration, contact time, temperature and presence of co-ions in the medium, were investigated. The structures and adsorption performances of the adsorbents were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Compared with other AC-TFR adsorbents, AC-TFR-2 (mass ratio of AC:TFR = 1:1) showed an excellent adsorption capacity based on the efficiency of Cr(VI) removal. The kinetic data fitted to pseudo-second-order and intra-particle diffusion models suggested that the adsorption process was subject to a rate-controlling step. The equilibrium adsorption data fitted well to the Langmuir isotherm model, and the maximum adsorption capacities of AC-TFR-2 were 145.99, 167.22 and 174.52 mg/g at 288, 298, and 308 K, respectively. The thermodynamic parameters revealed that Cr(VI) removal by AC-TFR-2 was endothermic and spontaneous, and the process was chemical adsorption. The mechanism of Cr(VI) removal consisted first of reduction to Cr(III), which has a low toxicity, and then chelation onto AC-TFR-2 via ion exchange.

scholarly journals Fabrication of Carboxymethylcellulose/Metal-Organic Framework Beads for Removal of Pb(II) from Aqueous Solution

Materials ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 942 ◽  
Author(s):  
Huo-Xi Jin ◽  
Hong Xu ◽  
Nan Wang ◽  
Li-Ye Yang ◽  
Yang-Guang Wang ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Langmuir Isotherm ◽  
Adsorption Equilibrium ◽  
Isotherm Model ◽  
Maximum Adsorption Capacity ◽  
X Ray ◽  
Metal Organic ◽  
Langmuir Isotherm Model

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.

scholarly journals Husk of Agarwood Fruit-Based Hydrogel Beads for Adsorption of Cationic and Anionic Dyes in Aqueous Solutions

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1437
Author(s):  
Chih Ming Ma ◽  
Bo-Yuan Yang ◽  
Gui-Bing Hong
Keyword(s):  
Aqueous Solutions ◽  
Selective Adsorption ◽  
Order Model ◽  
Anionic Dyes ◽  
Adsorption Selectivity ◽  
Hydrogel Beads ◽  
Batch System ◽  
Initial Ph ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order

Hydrogel beads based on the husk of agarwood fruit (HAF)/sodium alginate (SA), and based on the HAF/chitosan (CS) were developed for the removal of the dyes, crystal violet (CV) and reactive blue 4 (RB4), in aqueous solutions, respectively. The effects of the initial pH (2–10) of the dye solution, the adsorbent dosage (0.5–3.5 g/L), and contact time (0–540 min) were investigated in a batch system. The dynamic adsorption behavior of CV and RB4 can be represented well by the pseudo-second-order model and pseudo-first-order model, respectively. In addition, the adsorption isotherm data can be explained by the Langmuir isotherm model. Both hydrogel beads have acceptable adsorption selectivity and reusability for the study of selective adsorption and regeneration. Based on the effectiveness, selectivity, and reusability of these hydrogel beads, they can be treated as potential adsorbents for the removal of dyes in aqueous solutions.

Adsorption of PtCl62− from Hydrochloric Acid Solution by Chemically Modified Lignin Based on Rice Straw

2018 ◽  
Vol 71 (12) ◽  
pp. 931 ◽  
Author(s):  
Baoping Zhang ◽  
Bowen Shen ◽  
Meichen Guo ◽  
Yun Liu
Keyword(s):  
Hydrochloric Acid ◽  
Acid Solution ◽  
Rice Straw ◽  
Hydrochloric Acid Solution ◽  
Photoelectron Spectroscopy ◽  
Selective Adsorption ◽  
Adsorption Time ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Modified Lignin

A novel adsorbent with the properties of selective adsorption based on rice straw was used to adsorb PtCl62− from hydrochloric acid solution by batch sorption. Many influencing factors for PtCl62− adsorption, such as initial concentration of PtCl62−, adsorption time, and concentration of hydrochloric acid, were optimized. The results suggested that the saturation adsorption capacity of PtCl62− was 218.8mgg−1 and the equilibrium adsorption time was 120min. The adsorbent had excellent selectivity on PtCl62− when the concentration of hydrochloric acid was lower than 0.5molL−1. The adsorption fitted well with the Langmuir isotherm model and pseudo-second-order kinetics model. The adsorption mechanism was investigated by FT-IR and X-ray photoelectron spectroscopy analyses and it indicated that PtIV was reduced to PtII by hydroxy groups and then coordinated with N through ion exchange between Cl− and PtCl42−.

Property of Cu2O-CuO/ZSM-5 nanocomposite and degradation process of azo dye AO7 without sacrificial agent (H2O2)

2016 ◽  
Vol 73 (11) ◽  
pp. 2747-2753 ◽  
Author(s):  
Wusong Kong ◽  
Hongxia Qu ◽  
Peng Chen ◽  
Weihua Ma ◽  
Huifang Xie
Keyword(s):  
Catalytic Activity ◽  
Aqueous Solutions ◽  
Photoelectron Spectroscopy ◽  
Oxygen Demand ◽  
Operating Conditions ◽  
Surface Element ◽  
Impregnation Method ◽  
X Ray ◽  
Initial Ph ◽  
Sacrificial Agent

In this study, Cu2O-CuO/ZSM-5 nanocomposite was synthesized by the impregnation method, and its catalytic performance for the destruction of AO7 in aqueous solutions was investigated. The morphology, structure and surface element valence state of Cu2O-CuO/ZSM-5 were characterized by transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The operating conditions on the degradation of AO7 by Cu2O-CuO/ZSM-5, such as initial pH values, concentration of AO7 and catalyst dosage were investigated and optimized. The results showed that the sample had good catalytic activity for destruction of AO7 in the absence of a sacrificial agent (e.g. H2O2): it could degrade 91% AO7 in 140 min at 25 °C and was not restricted by the initial pH of the AO7 aqueous solutions. Cu2O-CuO/ZSM-5 exhibited stable catalytic activity with little loss after three successive runs. The total organic carbon and chemical oxygen demand removal efficiencies increased rapidly to 69.36% and 67.3% after 120 min of treatment by Cu2O-CuO/ZSM-5, respectively.

scholarly journals Enhanced removal of hexavalent chromium by different acid-modified biochar derived from corn straw: behavior and mechanism

2020 ◽  
Vol 81 (10) ◽  
pp. 2270-2280
Author(s):  
Yonggang Xu ◽  
Tianxia Bai ◽  
Yubo Yan ◽  
Yunfeng Zhao ◽  
Ling Yuan ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Hydrogen Ion ◽  
Corn Straw ◽  
Order Model ◽  
Freundlich Model ◽  
X Ray ◽  
Modified Biochar ◽  
Before And After ◽  
Pseudo Second Order ◽  
Kinetics Of

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).

scholarly journals Synthesis of Nanoscale Zerovalent Iron (nZVI) Supported on Biochar for Chromium Remediation from Aqueous Solution and Soil

2019 ◽  
Vol 16 (22) ◽  
pp. 4430 ◽  
Author(s):  
Haixia Wang ◽  
Mingliang Zhang ◽  
Hongyi Li
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Zero Valent Iron ◽  
Zerovalent Iron ◽  
X Ray ◽  
Nanoscale Zerovalent Iron ◽  
Before And After ◽  
Pseudo Second Order ◽  
Xrd Patterns ◽  
Co Precipitation

Maize straw biochar-supported nanoscale zero-valent iron composite (MSB-nZVI) was prepared for efficient chromium (Cr) removal through alleviating the aggregation of zero-valent iron particles. The removal mechanism of MSB-nZVI was investigated by scanning electron microscopy with energy dispersive X-ray (SEM-EDX), X-ray diffractometry (XRD), and X-ray photoelectron spectroscopy (XPS). Cr(VI) removal from aqueous solution by MSB-nZVI was greatly affected by pH and initial concentration. The removal efficiency of Cr(VI) decreased with increasing pH, and the removal kinetics followed the pseudo-second-order model. XRD patterns of MSB-nZVI before and after reaction showed that reduction and precipitation/co-precipitation (FeCr2O4, Fe3O4, Fe2O3) occurred with the conversion of Cr(VI) to Cr(III) and Fe(0) to Fe(II)/Fe(III). The produced precipitation/co-precipitation could be deposited on the MSB surface rather than being only coated on the surface of nZVI particles, which can alleviate passivation of nZVI. For remediation of Cr(VI)-contaminated saline–alkali soil (pH 8.6–9.0, Cr 341 mg/kg), the released amount of Cr(VI) was 70.7 mg/kg, while it sharply decreased to 0.6–1.7 mg/kg at pH 4.0–8.0, indicating that the saline–alkali environment inhibited the remediation efficiency. These results show that MSB-nZVI can be used as an effective material for Cr(VI) removal from aqueous solution and contaminated soil.

scholarly journals Adsorption of As(V) by the Novel and Efficient Adsorbent Cerium-Manganese Modified Biochar

Water ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2720
Author(s):  
Ting Liang ◽  
Lianfang Li ◽  
Changxiong Zhu ◽  
Xue Liu ◽  
Hongna Li ◽  
...  
Keyword(s):  
Manganese Oxide ◽  
Photoelectron Spectroscopy ◽  
Water Environment ◽  
Polluted Water ◽  
X Ray ◽  
Modified Biochar ◽  
Wide Ph Range ◽  
Infrared Spectrometer ◽  
Pseudo Second Order ◽  
Ph Range

Arsenic has become a global concern in water environment, and it is essential to develop efficient remediation methods. In this study, a novel adsorbent by loading cerium and manganese oxide onto wheat straw-modified biochar (MBC) was manufactured successfully aiming to remove arsenic from polluted water. Through scanning electron microscopy and energy-dispersive spectroscopy (SEM-EDS), X-ray diffractometer (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectrometer (FT-IR), and other techniques, it was found the loading of cerium and manganese oxide on MBC played a significant role in As(V) adsorption. The results of the batch test showed that the adsorption of MBC followed the pseudo-second order kinetics and Langmuir equation. The adsorption capacity of MBC was 108.88 mg As(V)/g at pH = 5.0 (C0 = 100 mg/L, dosage = 0.5 g/L, T = 298 K) with considerable improvement compared to the original biochar. Moreover, MBC exhibited excellent performance over a wide pH range (2.0~11.0). Thermodynamics of the sorption reaction showed that the entropy (ΔS), changes of enthalpy (ΔH) and Gibbs free energy (ΔG), respectively, were 85.88 J/(moL·K), 22.54 kJ/mol and −1.33 to −5.20 kJ/mol at T = 278~323 K. During the adsorption, the formation of multiple complexes under the influence of its abundant surface M-OH (M represents the Ce/Mn) groups involving multiple mechanisms that included electrostatic interaction forces, surface adsorption, redox reaction, and surface complexation. This study indicated that MBC is a promising adsorbent to remove As(V) from polluted water and has great potential in remediating of arsenic contaminated environment.

Sign in / Sign up

Export Citation Format

Share Document