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

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.

2022 ◽  
Author(s):  
Chuqing Yao ◽  
Yaodong Dai ◽  
Shuquan Chang ◽  
Haiqian Zhang

Abstract In this work, novel Prussian blue tetragonal nanorods were prepared by template-free solvothermal methods for removal of radionuclide Cs and Sr. It was worth that Prussian blue nanorods exhibited the better adsorption performance than co-precipitation PB or Prussian blue analogue composites. Thermodynamic analysis implied that adsorption process was spontaneous and endothermic which was described well with Langmuir isotherm and pseudo-second-order equation, the maximum adsorption capacity of PB nanorod was estimated to be 194.26 mg g-1 and 256.62 mg g-1 for Cs+ and Sr2+. The adsorption mechanism of Cs+ and Sr2+ was studied by X-ray photoelectron spectroscopy, X-ray diffraction and 57Fe Mössbaure spectroscopy, the results revealed that Cs+ entered in PB crystal to generate a new phase, the most of Sr2+ was trapped in internal crystal and the other exchanged Fe2+. Furthermore, the effect of co-existing ions and pH for PB adsorption process were also investigated. The results suggest that PB nanorods were outstanding candidate for removal of Cs+ and Sr2+ from radioactive wastewater.


2020 ◽  
Vol 81 (5) ◽  
pp. 936-948 ◽  
Author(s):  
Xubing Sun ◽  
Jiayong Zhang ◽  
Guowen Ding ◽  
Yaohui You

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.


Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1125
Author(s):  
Bhoj Raj Poudel ◽  
Ram Lochan Aryal ◽  
Sitaram Bhattarai ◽  
Agni Raj Koirala ◽  
Surendra Kumar Gautam ◽  
...  

A novel type of adsorbent, TiO2 impregnated pomegranate peels (PP@TiO2) was successfully synthesized and its efficacy was investigated based on the removal of As(III) from water. The adsorbent was characterized using Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectrometer (EDS), X-ray Diffraction (XRD) analysis, and Fourier Transform Infrared (FTIR) Spectroscopy, to evaluate its morphology, elemental analysis, crystallinity, and functional groups, respectively. Batch experiments were conducted on PP@TiO2 for As(III) adsorption to assess the adsorption isotherm, effect of pH, and adsorption kinetics. Characterization data suggested that TiO2 was successfully impregnated on the biomass substrate. The equilibrium data better fitted to the Langmuir isotherm model having a maximum adsorption capacity of 76.92 mg/g and better distribution coefficients (KD) in the order of ~103 mL/g. The highest percentage of adsorption was found at neutral pH. The adsorption kinetics followed the pseudo-2nd-order model. X-ray Photoelectron Spectroscopy (XPS) of the adsorption product exhibited that arsenic was present as As(III) and partially oxidized to As(V). PP@TiO2 can work effectively in the presence of coexisting anions and could be regenerated and reused. Overall, these findings suggested that the as-prepared PP@TiO2 could provide a better and efficient alternative for the synergistic removal of As(III) from water.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamed S. Yahia ◽  
Ahmed S. Elzaref ◽  
Magdy B. Awad ◽  
Ahmed M. Tony ◽  
Ahmed S. Elfeky

Abstract Commercial Granulated Active Carbon (GAC) has been modified using 10 Gy dose Gamma irradiation (GAC10 Gy) for increasing its ability of air purification. Both, the raw and treated samples were applied for removing Chlorpyrifos pesticide (CPF) from ambient midair. Physicochemical properties of the two materials were characterized by Fourier Transform Infrared (FT-IR) and Raman spectroscopy. The phase formation and microstructure were monitored using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), supported with Energy-Dispersive X-ray (EDX). The Surface area measurement was detected using BET particle size prosometry. Obtained outcomes showed that, the maximum adsorption capacity, given by Langmuir equations, was greatly increased from 172.712 to 272.480 mg/g for GAC and GAC10 Gy, respectively, with high selectivity. The overall removal efficiency of GAC10 Gy was notably comparable to that of the original GAC-sorbent. The present study indicated that, gamma irradiation could be a promising technique for treating GAC and turned it more active in eliminating the pesticides pollutants from surrounding air. The data of equilibrium has been analyzed by Langmuir and Freundlich models, that were considerably better suited for the investigated materials than other models. The process kinetics of CPF adsorbed onto both tested carbon versions were found to obey the pseudo first order at all concentrations with an exception at 70 mg/l using GAC, where, the spontaneous exothermic adsorption of Chlorpyrifos is a strong function for the pseudo-first order (PFO) and pseudo second order (PSO) kinetics.


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.


Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil

The sorption of uranium and thorium from their aqueous solutions by using 8-hydroxyquinoline modified Na-bentonite (HQ-bentonite) was investigated by the batch technique. Na-bentonite and HQ-bentonite were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier Transform Infrared (FTIR) spectroscopy. Factors that influence the sorption of uranium and thorium onto HQ-bentonite such as solution pH, contact time, initial metal ions concentration, HQ-bentonite mass, and temperature were tested. Sorption experiments were expressed by Freundlich and Langmuir isotherms and the sorption results demonstrated that the sorption of uranium and thorium onto HQ-bentonite correlated better with the Langmuir isotherm than the Freundlich isotherm. Kinetics studies showed that the sorption followed the pseudo-second-order kinetic model. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° indicated that the sorption of uranium and thorium onto HQ-bentonite was endothermic, feasible, spontaneous, and physical in nature. The maximum adsorption capacities of HQ-bentonite were calculated from the Langmuir isotherm at 303 K and were found to be 63.90 and 65.44 for U(VI) and Th(IV) metal ions, respectively.


Author(s):  
Haixia Wang ◽  
Mingliang Zhang ◽  
Hongyi Li

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.


Molecules ◽  
2019 ◽  
Vol 24 (8) ◽  
pp. 1449 ◽  
Author(s):  
Xianchun Hu ◽  
Xianfeng Du

Microporous starch (MPS) granules were formed by the partial hydrolysis of starch using α–amylase and glucoamylase. Due to its biodegradability and safety, MPS was employed to adsorb tea polyphenols (TPS) based on their microporous characteristics. The influences of solution pH, time, initial concentration and temperature on the adsorptive capacity were investigated. The adsorption kinetics data conformed to the pseudo second–order kinetics model, and the equilibrium adsorption data were well described by the Langmuir isotherm model. According to the fitting of the adsorption isotherm formula, the maximum adsorption capacity of TPS onto MPS at pH 6.7 and T = 293 K was approximately 63.1 mg/g. The thermodynamic parameters suggested that the adsorption of TPS onto MPS was spontaneous and exothermic. Fourier transform infrared (FT–IR) analysis and the thermodynamics data were consistent with a physical adsorption mechanism. In addition, MPS-loaded TPS had better stability during long-term storage at ambient temperature.


Materials ◽  
2019 ◽  
Vol 12 (2) ◽  
pp. 218 ◽  
Author(s):  
Alfred Mensah ◽  
Pengfei Lv ◽  
Christopher Narh ◽  
Jieyu Huang ◽  
Di Wang ◽  
...  

In this study, a novel green adsorbent material prepared by the esterification of bacterial cellulose (BC) and graphene oxide (GO), richly containing hydroxyl, alkyl, and carboxylate groups was characterised by FTIR (Fourier Transform infrared spectroscopy), XRD (X-ray diffraction), SEM (Scanning electron microscopy) and TGA (Thermo-graphimetric analysis). The specific surface area (SSA) and pore size distribution (PSD) analysis of materials were also analysed. Batch experiments–adsorption studies confirmed the material to have a very high Pb2+ removal efficiency of over 90% at pH 6–8. Kinetic studies showed that the uptake of metal ions was rapid with equilibrium attained after 30 min and fitted well with the pseudo-second-order rate model (PSO). Isotherm results with a maximum adsorption capacity (Qmax) of 303.03 mg/g were well described by Langmuir’s model compared to Freundlich. Desorption and re-adsorption experiments realised that both adsorbent and adsorbates could be over 90–95% efficiently recovered and reused using 0.1 M HNO3 and 0.1 M HCl.


2016 ◽  
Vol 6 (4) ◽  
pp. 544-552 ◽  
Author(s):  
H. Godini ◽  
F. Hashemi ◽  
L. Mansuri ◽  
M. Sardar ◽  
Ghasem Hassani ◽  
...  

The present paper aims to investigate water purification of phenol by walnut green hull adsorbent. The surface characteristics of the adsorbent were studied using Fourier transform infra-red (FTIR), scanning electron microscope, and X-ray diffraction (XRD) techniques. The presence of functional groups such as hydroxyl and carbonyl onto walnut green hull surface was proved by FTIR analysis. Also quartz, cellulose and hematite were detected in the XRD analysis of samples by an X-ray diffractometer. The maximum sorption was achieved at pH 4.0. Data were evaluated for compliance with the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. The results indicate that the data for adsorption of phenol onto walnut green hull fitted well with the Langmuir isotherm. The maximum adsorption capacity of the adsorbent was achieved by Langmuir isotherm 17.8 mg g–1. Also, the adsorption kinetics of phenol on the adsorbent were studied. The rates of sorption were found to conform to pseudo-second-order kinetics with good correlation.


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