Reduction of highly concentrated phosphate from aqueous solution using pectin-nanoscale zerovalent iron (PNZVI)

2016 ◽  
Vol 73 (11) ◽  
pp. 2689-2696 ◽  
Author(s):  
Hongyu Wang ◽  
Zhuocheng Zou ◽  
Xuelian Xiao ◽  
Dan Chen ◽  
Kai Yang

Pectin-nanoscale zerovalent iron (PNZVI) has been studied as an effective phosphate adsorption material to remove highly concentrated phosphate from aqueous solution. Batch phosphate removal and equilibrium experiments were conducted in order to evaluate the effects of environmental factors such as pH, coexisting anions and ionic strengths on phosphate removal by PNZVI. The scanning electron microscope images of nanoscale zerovalent iron (NZVI) and PNZVI demonstrated that PNZVI exhibited larger specific surface areas than NZVI so that PNZVI had higher phosphate removal efficiency than NZVI. Equilibrium experiments showed that phosphate adsorption by PNZVI was well fitted with the Freundlich and Langmuir models. In addition, the maximum adsorption capacity reached 277.38 mgP/gPNZVI. The ionic strengths and common anions showed no significant effects on the process of phosphate adsorption by PNZVI. The phosphate removal efficiency increased to a peak value with pH increased from 2.0 to 5.0, then decreased with pH further increased from 5.0 to 10.0. The Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses of PNZVI and P-loaded PNZVI indicated that adsorption, rather than redox reaction, was the dominant mechanism for the removal of phosphate by PNZVI.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jien Ye ◽  
Yi Wang ◽  
Qiao Xu ◽  
Hanxin Wu ◽  
Jianhao Tong ◽  
...  

AbstractPassivation of nanoscale zerovalent iron hinders its efficiency in water treatment, and loading another catalytic metal has been found to improve the efficiency significantly. In this study, Cu/Fe bimetallic nanoparticles were prepared by liquid-phase chemical reduction for removal of hexavalent chromium (Cr(VI)) from wastewater. Synthesized bimetallic nanoparticles were characterized by transmission electron microscopy, Brunauer–Emmet–Teller isotherm, and X-ray diffraction. The results showed that Cu loading can significantly enhance the removal efficiency of Cr(VI) by 29.3% to 84.0%, and the optimal Cu loading rate was 3% (wt%). The removal efficiency decreased with increasing initial pH and Cr(VI) concentration. The removal of Cr(VI) was better fitted by pseudo-second-order model than pseudo-first-order model. Thermodynamic analysis revealed that the Cr(VI) removal was spontaneous and endothermic, and the increase of reaction temperature facilitated the process. X-ray photoelectron spectroscopy (XPS) analysis indicated that Cr(VI) was completely reduced to Cr(III) and precipitated on the particle surface as hydroxylated Cr(OH)3 and CrxFe1−x(OH)3 coprecipitation. Our work could be beneficial for the application of iron-based nanomaterials in remediation of wastewater.


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.


2018 ◽  
Vol 5 (1) ◽  
pp. 171662 ◽  
Author(s):  
Bin Feng ◽  
Wenzhong Shen ◽  
Liyi Shi ◽  
Shijie Qu

Owing to the unique microporous structure and high specific surface area, porous carbon could act as a good carrier for functional materials. In this paper, polyacrylonitrile (PAN)-based porous carbon materials (PPC-0.6-600, PPC-0.8-600, PPC-0.6-800 and PPC-0.8-800) were prepared by heating KOH at 600°C and 800 o C for the removal of Cr(VI) from aqueous solution. The adsorbent was characterized by the techniques of Fourier transform infrared spectroscopy (FT-IR), elementary analysis, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and N 2 adsorption techniques. The results showed that the adsorption capacity increased with decreasing pH value of the initial solution. The adsorption capacity of Cr(VI) on PPC-0.8-800 was much greater than that on other materials, and maximum adsorption capacity were calculated to be 374.90 mg g −1 . Moreover, PPC-0.8-800 had superior recyclability for the removal of Cr(VI) from wastewater, about 82% of its initial adsorption capacity was retained even after five cycles. The result of kinetic simulation showed that the adsorption of Cr(VI) on the PAN-based porous carbon could be described by pseudo-second-order kinetics. The adsorption process was the ionic interaction between protonated amine groups of PPC and HCrO 4 - ions.


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.


Water ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 781 ◽  
Author(s):  
Wang ◽  
Zhang ◽  
Lv

The removal efficiency and mechanism of Cr(VI) removal from aqueous solution on semi-decomposed maize straw biochars pyrolyzed at 300 to 600 °C were investigated. The removal of Cr(VI) by the biochars decreased with pyrolysis temperature increasing from 300 to 600 °C, and the maximum removal capacity of Cr(VI) for maize straw biochar pyrolyzed at 300 °C was 91 mg/g at pH 2.0. The percentage removal of Cr(VI) rapidly decreased with pH increasing from 2.0 to 8.0, with the maximum (>99.9%) at pH 2.0. The variation of Cr(VI) and Cr(III) concentrations in the solution after reaction showed that Cr(VI) concentration decreased while Cr(III) increased and the equilibrium was reached after 48 h, while the redox potential after reaction decreased due to Cr(VI) reduction. X-ray photoelectron spectroscopy (XPS) semi-quantitative analysis showed that Cr(III) accounted for 75.7% of the total Cr bound to maize straw biochar, which indicated reductive adsorption was responsible for Cr(VI) removal by the biochars. Cr(VI) was firstly adsorbed onto the positively charged biochar surface and reduced to Cr(III) by electrons provided by oxygen-containing functional groups (e.g., C=O), and subsequently part of the converted Cr(III) remained on the biochar surface and the rest released into solution. Fourier transform infrared (FTIR) data indicated the participation of C=O, Si–O, –CH2 and –CH3 groups in Cr(VI) removal by the biochars. This study showed that maize straw biochar pyrolyzed at 300 °C for 2 h was one low-cost and efficient adsorbent for Cr(VI) removal from aqueous solution.


2017 ◽  
Vol 70 ◽  
pp. 183-189 ◽  
Author(s):  
Guodong Sheng ◽  
Xiangxian Ma ◽  
Wensheng Linghu ◽  
Zhongshan Chen ◽  
Jun Hu ◽  
...  

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