scholarly journals Improved Affinity of Nanoscale Zero Valent Iron toward Hydrophobic Organic Solvent using Poly(1-vinylpyrrolidone-co-vinyl acetate)

2020 ◽  
Vol 42 (9) ◽  
pp. 431-441
Author(s):  
Jeongmin Hong ◽  
Hayeon Yang ◽  
Taeyeon Cha ◽  
Younggyo Seo ◽  
Yuhoon Hwang

Objectives : Levels of organic contaminants in excess of the standard minimum have been detected in many commercial and residential sites, and the severity of soil and groundwater pollution is increasing. In particular, non-aqueous phase liquids (NAPLs) are hydrophobic organic pollutants that do not mix with water and are difficult to remove with existing soil remediation technology. These pollutants slowly dissolve into the groundwater over long periods of time, thus contaminating the groundwater. With the increasing need to remove NAPLs for soil and groundwater remediation, widespread interest has focused on the use of nanoscale zero valent iron (nZVI). However, nZVI has the disadvantage of reduced subsurface mobility. Hence, in the present study, the nZVI surface is modified with poly(1-vinylpyrrolidone-co-vinyl acetate) (PVP/VA), which has both hydrophilic and hydrophobic groups, to improve the mobility and selectivity of nZVI for the removal of NAPL.Methods : The PVP/VA modified nZVI is synthesized through the reaction of FeSO4・7H2O and NaBH4 in the presence of PVP/VA. To confirm the dispersibility of the prepared material, a precipitation experiment is performed using a visible light spectrometer, and the mobility through a sand-filled column is evaluated. In addition, the variation in particle size and characteristics according to the presence of PVP/VA is examined via transmission electron microscopy. The nitrate reduction ability of nZVI with PVP/VA is also evaluated to reveal changes in reactivity depending upon the degree of dispersion. To confirm the selective mobility towards NAPL, trichloroethylene and dodecane are used to evaluate the mobility with and without PVP/VA. Finally, the ratio of nZVI passing through the sponge layer absorbing dodecane is evaluated to determine the selective mobility towards NAPL in the porous medium.Results and Discussion : Although the dispersibility of the PVP/VA-nZVI is not significantly changed, the particle size is significantly decreased. Both the mobility in porous media and the nitrate reduction rate are improved via PVP/VA modification. The affinity for hydrophobic contaminants and the selective migration of PVP/VA-nZVI towards the NAPL layer are also improved. The high affinity for the NAPL was also shown by the column with NAPL layer.Conclusions : Surface-modification with PVP/VA, which has both hydrophilic and hydrophobic ends, enabled the synthesis of nZVI with a smaller and more uniform particle size, thus providing high mobility in porous media and high reactivity towards contaminants. The combined hydrophilicity and hydrophobicity of PVP/VA is shown to increase the affinity of nZVI towards NAPL and, thus, promote its migration to the NAPL layer. Thus, it is anticipated that the efficiency of soil remediation can be improved by promoting the movement of nZVI towards the target NAPL layer.

2010 ◽  
Vol 61 (3) ◽  
pp. 705-712 ◽  
Author(s):  
Y. H. Hwang ◽  
D. G. Kim ◽  
Y. T. Ahn ◽  
C. M. Moon ◽  
H. S. Shin

This study investigates the fate of nitrogen species during nitrate reduction by nanoscale zero valent iron (NZVI) as well as the related kinetics. The NZVI used for the experiments was prepared by chemical reduction without a stabilizing agent. The pseudo first order kinetic constant of nitrate reduction at 30°C with an NZVI/nitrate ratio of 1.25:1, which were the reference conditions of this study, was 4.08 h−1 (R2 = 0.955). A nitrogen mass balance was established by quantitative analysis of aqueous-phase and gas-phase nitrogen species. The results confirm that the nitrate was converted to ammonium ion, that ammonia stripping subsequently occurred under a strong alkaline condition, and that the total amount of aqueous nitrogen was consequently reduced. The nitrate reduction rate also increased with a lower pH and a higher temperature when microscale ZVI was used. However, in contrast to the reaction by microscale ZVI, the nitrate reduction rate by NZVI was higher for an unbuffered condition, possibly due to the abundance of surface atoms and the smaller size.


2013 ◽  
Vol 726-731 ◽  
pp. 677-682
Author(s):  
Run Hua Liao ◽  
Yu Miao ◽  
Yan Hong ◽  
Yue Ming Li ◽  
Zong Yang Shen ◽  
...  

Porous suspended ceramsite (PSC) supported nanoscale zero valent iron (NZVI/PSC) were applied to the reductive removal of nitrate to investigate the effects. XRD, SEM and EDS analyses on NZVI/PSC revealed that PSC had loaded some nanoparticles, whose size was about 50 nm. Nitrate reduction rate of NZVI/PSC reached about 80% in 60 min, while the PSC unsupported nanozerovalent iron performed poorly with only 8% removal of the nitrate. Furthmore, during the reactions of NZVI/PSC and PSC with nitrate, for the NZVI/PSC, pH change was the greatest, while the reaction with PSC (this particles shows the lowest reactivity for nitrate reduction) resulted in the least pH change.


2017 ◽  
Vol 76 (7) ◽  
pp. 1827-1832 ◽  
Author(s):  
Jun Zhou ◽  
Qianyu Sun ◽  
Dan Chen ◽  
Hongyu Wang ◽  
Kai Yang

In this study, the hydrogenotrophic denitrifying bacterium Ochrobactrum anthropi was added in to the process of nitrate removal by starch-stabilized nanoscale zero valent iron (nZVI) to minimize undesirable ammonium. The ammonium control performance and cooperative mechanism of this combined process were investigated, and batch experiments were conducted to discuss the effects of starch-stabilized nZVI dose, biomass, and pH on nitrate reduction and ammonium control of this system. The combined system achieved satisfactory performance because the anaerobic iron corrosion process generates H2, which is used as an electron donor for the autohydrogenotrophic bacterium Ochrobactrum anthropi to achieve the autohydrogenotrophic denitrification process converting nitrate to N2. When starch-stabilized nZVI dose was increased from 0.5 to 2.0 g/L, nitrate reduction rate gradually increased, and ammonium yield also increased from 9.40 to 60.51 mg/L. Nitrate removal rate gradually decreased and ammonium yield decreased from 14.93 to 2.61 mg/L with initial OD600 increasing from 0.015 to 0.080. The abiotic Fe0 reduction process played a key role in nitrate removal in an acidic environment and generated large amounts of ammonium. Meanwhile, the nitrate removal rate decreased and ammonium yield also reduced in an alkaline environment.


2012 ◽  
Vol 133 (1) ◽  
pp. 205-211 ◽  
Author(s):  
H.B. Liu ◽  
T.H. Chen ◽  
D.Y. Chang ◽  
D. Chen ◽  
Y. Liu ◽  
...  

2020 ◽  
Vol 7 (4) ◽  
pp. 045002
Author(s):  
Shang-Qun Li ◽  
Chuang Yu ◽  
Ze-Xiang Wu ◽  
Xiao-Qing Cai ◽  
Fu-Sheng Zha

2018 ◽  
Vol 32 (3) ◽  
pp. 243-251 ◽  
Author(s):  
Youngpyoe Hong ◽  
Younggyo Seo ◽  
Hyowon Kim ◽  
Yuhoon Hwang

Author(s):  
Heli Wang ◽  
Yin Zhong ◽  
Xifen Zhu ◽  
Dan Li ◽  
Yirong Deng ◽  
...  

Modification of nanoscale zero-valent iron (nZVI) with reducing sulfur compounds has proven to improve the reactivity of nZVI towards recalcitrant halogenated organic contaminants.


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