Toxicity studies considering both the bare and stabilized forms of zero valent iron nanoparticles（nZVI） could be timely, given that ecological risks identified are minimized through modification or with substitution...Toxicity studies considering both the bare and stabilized forms of zero valent iron nanoparticles（nZVI） could be timely, given that ecological risks identified are minimized through modification or with substitution of approaches in the synthesis, development and environmental application of the nanoparticles before succeeding to volume production.This review is focused on the fate, transport and toxicological implications of the bare nZVI and surface modified particles used for environmental applications.展开更多
Excess phosphorus from non-point pollution sources is one of the key factors causing eutrophication in many lakes in China,so finding a cost-effective method to remove phosphorus from non-point pollution sources is ve...Excess phosphorus from non-point pollution sources is one of the key factors causing eutrophication in many lakes in China,so finding a cost-effective method to remove phosphorus from non-point pollution sources is very important for the health of the aqueous environment. Graphene was selected to support nanoscale zero-valent iron（nZVI）for phosphorus removal from synthetic rainwater runoff in this article. Compared with nZVI supported on other porous materials,graphene-supported nZVI（G-nZVI） could remove phosphorus more efficiently. The amount of nZVI in G-nZVI was an important factor in the removal of phosphorus by G-nZVI,and G-nZVI with 20 wt.% nZVI（20% G-nZVI）could remove phosphorus most efficiently. The nZVI was very stable and could disperse very well on graphene,as characterized by transmission electron microscopy（TEM） and scanning electron microscopy（SEM）. X-ray photoelectron spectroscopy（XPS）,Fourier Transform infrared spectroscopy（FT-IR） and Raman spectroscopy were used to elucidate the reaction process,and the results indicated that Fe-O-P was formed after phosphorus was adsorbed by G-nZVI. The results obtained from X-ray diffraction（XRD） indicated that the reaction product between nZVI supported on graphene and phosphorus was Fe3（PO4）2·8H2O（Vivianite）. It was confirmed that the specific reaction mechanism for the removal of phosphorus with nZVI or G-nZVI was mainly due to chemical reaction between nZVI and phosphorus.展开更多
We explored the feasibility and removal mechanism of removing 2-chlorobiphenyl（2-Cl BP）from soil–water system using granular activated carbon（GAC） impregnated with nanoscale zerovalent iron（reactive activated ca...We explored the feasibility and removal mechanism of removing 2-chlorobiphenyl（2-Cl BP）from soil–water system using granular activated carbon（GAC） impregnated with nanoscale zerovalent iron（reactive activated carbon or RAC）.The RAC samples were successfully synthesized by the liquid precipitation method.The mesoporous GAC based RAC with low iron content（1.32%） exhibited higher 2-Cl BP removal efficiency（54.6%） in the water phase.The result of Langmuir–Hinshelwood kinetic model implied that the different molecular structures between 2-Cl BP and trichloroethylene（TCE） resulted in more difference in dechlorination reaction rates on RAC than adsorption capacities.Compared to removing2-Cl BP in the water phase,RAC removed the 2-Cl BP more slowly in the soil phase due to the significant external mass transfer resistance.However,in the soil phase,a better removal capacity of RAC was observed than its base GAC because the chemical dechlorination played a more important role in total removal process for 2-Cl BP.This important result verified the effectiveness of RAC for removing 2-Cl BP in the soil phase.Although reducing the total RAC removal rate of 2-Cl BP,soil organic matter（SOM）,especially the soft carbon,also served as an electron transfer medium to promote the dechlorination of 2-Cl BP in the long term.展开更多
Nanosized zero-valent iron (NZVI) supported on the cation exchange resin was synthesized and applied to decompose some water soluble azo dyes. The decomposition efficiency for azo dyes was evaluated by using the aqueo...Nanosized zero-valent iron (NZVI) supported on the cation exchange resin was synthesized and applied to decompose some water soluble azo dyes. The decomposition efficiency for azo dyes was evaluated by using the aqueous suspensions and parked column of this material. Batch experiments indicated that this novel material exhibited excellent degradation ability for 0.05 g·L1 of Acid Orange 7, Acid Orange 8, Acid Orange 10, Sunset Yellow, and Methyl Orange, with decolorization ratio up to 95% in 4 min; pH value was the key factor for degradation and H+ was one of the reactants; adsorption of azo dyes onto the material existed at the beginning but reduced gradually until disappearing completely. For the packed column system, 58%~90% of azo dyes were decomposed in the 1st circle of solution passing through the column, and the adsorption onto the materials could accelerate the degradation azo dyes with the increasing reaction time. During the degradation process, Fe2+, the product of NZVI, was exchanged to the resin again and could be reduced to Fe0 by KBH4 for reusing. The 10th refreshed NZVI possessed reductive activity up to 90% of the newly systhesized NZVI. Decomposing pollutants in the aqueous solution with columns packed with NZVI immobilized on the cation exchange resin is a promising technology that can solve the reclaiming and refreshing problem of NZVI.展开更多
Nanoscale zerovalent iron/magnetic carbon(NZVI/MC) composites were successfully synthesized by simply calcining yellow pine and iron precursors. NZVI/MC pyrolyzed at 800°C(NZVI/MC800) had a higher percentage of N...Nanoscale zerovalent iron/magnetic carbon(NZVI/MC) composites were successfully synthesized by simply calcining yellow pine and iron precursors. NZVI/MC pyrolyzed at 800°C(NZVI/MC800) had a higher percentage of NZVI and displayed better resistance to aggregation and oxidation of NZVI than samples prepared at other temperatures. The NZVI/MC800 material was applied for the elimination of U(Ⅵ) from aqueous solutions. The results suggested that the NZVI/MC800 displayed excellent adsorption capacity(203.94 mg/g)toward U(Ⅵ). The significant adsorption capacity and fast adsorption kinetics were attributed to the presence of well-dispersed NZVI, which could quickly reduce U(Ⅵ) into U(Ⅳ), trapping the guest U(Ⅳ) in the porous biocarbon matrix. The removal of U(Ⅵ) on the NZVI/MC samples was strongly affected by solution pH. The NZVI/MC samples also displayed outstanding reusability for U(Ⅵ) removal after multiple cycles. These findings indicate that NZVI/MC has great potential for remediation of wastewater containing U(Ⅵ).展开更多
Nano zero valent iron particles (nZVI) are popular the last few years because of the numerous applications in remediation of a wide range of pollutants in contaminated soils and aquifers. The nZVI particles can be 10 ...Nano zero valent iron particles (nZVI) are popular the last few years because of the numerous applications in remediation of a wide range of pollutants in contaminated soils and aquifers. The nZVI particles can be 10 - 1000 times more reactive than granular or micro-scale ZVI particles due to the small particle size, large specific surface area and high reactivity. An alternative green synthesis procedure was used for the production of nano zero valent iron particles (nZVI) using green tea (GT) extract, which is characterized by its high antioxidant content. Polyphenols in green tea extract possess double role in the synthesis of nZVI, because they not only reduce ferric cations, but also protect nZVI from oxidation and agglomeration as capping agents. The objective of current study was to simulate ata laboratory scale the attachment of GT-nZVI particles on soil material and study the effectiveness of attached nanoparticles for removing hexavalent chromium (Cr(VI)) from contaminated groundwater flowing through the porous soil bed. Column tests were carried out with various flowrates in order to examine the effect of contact time between the attached on porous medium nZVI and the flow-through solution on Cr(VI) reduction. After the completion of column tests the soil material in each column was split in 5 vertical sections, which were further subjected to chemical analyses and leaching tests. According to the results of the study increasing the contact time favors the reduction and removal of Cr(VI) from the aqueous phase. The reductive precipitation of Cr can be described as a reaction that follows a pseudo-first order kinetic law, with rate constant equal to k = 0.0243 ± 0.0011 min-1. Leaching tests indicated that precipitated chromium is not soluble. In the examined soil material, the total amount of precipitated Cr was found to range between 280 and 890 mg/(kg soil), while soluble Cr was less than 1.4 mg/kg and most probably it was due to the presence of residual Cr(VI) solution in the porosity of soil.展开更多
Nitrate is the leading cause of eutrophication worldwide and is one of the most challenging pollutants for restoration of polluted surface waters such as lakes, rivers and reservoirs. We report herein a new architectu...Nitrate is the leading cause of eutrophication worldwide and is one of the most challenging pollutants for restoration of polluted surface waters such as lakes, rivers and reservoirs. We report herein a new architecture of iron nanoparticles for high-efficiency denitrification by selective reduction of nitrate (NO3-) to dinitrogen (N2). The iron nanoparticles are doped with nitrogen (FeN) and encapsulated within a thin layer of nitride-carbon (NC). The nanoparticles have high pyrrolic N content (17.4 at.%) and large specific surface area (2040 m2/g). Laboratory experiments demonstrated high N2selectivity (91%) and nitrate removal capacity (6004 mg N/g Fe) for treatment of nitrate-containing water. This iron-based nanomaterial overcomes shortcomings of conventional catalysts by eliminating the use of precious and toxic heavy metals (e.g., Pd, Pt, Cu, Ni) and minimizing the generation of undesirable byproducts (e.g., ammonia) from the reactions with nanoscale zero-valent iron (n ZVI). The multiple electron transfers process from NO3- to N2can be fine-tuned by adjusting the NC shell thickness. Superior electrocatalytic perfor- mance, low cost and minimal environmental impact of the iron-derived nanocatalyst offer promising prospects for water purification, waste treatment and environmental remediation.展开更多
文摘Toxicity studies considering both the bare and stabilized forms of zero valent iron nanoparticles（nZVI） could be timely, given that ecological risks identified are minimized through modification or with substitution of approaches in the synthesis, development and environmental application of the nanoparticles before succeeding to volume production.This review is focused on the fate, transport and toxicological implications of the bare nZVI and surface modified particles used for environmental applications.
基金supported by the Major Science and Technology Programs for Water Pollution Control and Management of China (Nos.2011ZX07301-002 and 2012ZX07205-001)
文摘Excess phosphorus from non-point pollution sources is one of the key factors causing eutrophication in many lakes in China,so finding a cost-effective method to remove phosphorus from non-point pollution sources is very important for the health of the aqueous environment. Graphene was selected to support nanoscale zero-valent iron（nZVI）for phosphorus removal from synthetic rainwater runoff in this article. Compared with nZVI supported on other porous materials,graphene-supported nZVI（G-nZVI） could remove phosphorus more efficiently. The amount of nZVI in G-nZVI was an important factor in the removal of phosphorus by G-nZVI,and G-nZVI with 20 wt.% nZVI（20% G-nZVI）could remove phosphorus most efficiently. The nZVI was very stable and could disperse very well on graphene,as characterized by transmission electron microscopy（TEM） and scanning electron microscopy（SEM）. X-ray photoelectron spectroscopy（XPS）,Fourier Transform infrared spectroscopy（FT-IR） and Raman spectroscopy were used to elucidate the reaction process,and the results indicated that Fe-O-P was formed after phosphorus was adsorbed by G-nZVI. The results obtained from X-ray diffraction（XRD） indicated that the reaction product between nZVI supported on graphene and phosphorus was Fe3（PO4）2·8H2O（Vivianite）. It was confirmed that the specific reaction mechanism for the removal of phosphorus with nZVI or G-nZVI was mainly due to chemical reaction between nZVI and phosphorus.
基金supported by the National Natural Science Foundation of China(No.41201302)the Fundamental Research Funds for the Central Universities(No.222201514337)Shanghai Natural Science Funds(No.11ZR1409400)
文摘We explored the feasibility and removal mechanism of removing 2-chlorobiphenyl（2-Cl BP）from soil–water system using granular activated carbon（GAC） impregnated with nanoscale zerovalent iron（reactive activated carbon or RAC）.The RAC samples were successfully synthesized by the liquid precipitation method.The mesoporous GAC based RAC with low iron content（1.32%） exhibited higher 2-Cl BP removal efficiency（54.6%） in the water phase.The result of Langmuir–Hinshelwood kinetic model implied that the different molecular structures between 2-Cl BP and trichloroethylene（TCE） resulted in more difference in dechlorination reaction rates on RAC than adsorption capacities.Compared to removing2-Cl BP in the water phase,RAC removed the 2-Cl BP more slowly in the soil phase due to the significant external mass transfer resistance.However,in the soil phase,a better removal capacity of RAC was observed than its base GAC because the chemical dechlorination played a more important role in total removal process for 2-Cl BP.This important result verified the effectiveness of RAC for removing 2-Cl BP in the soil phase.Although reducing the total RAC removal rate of 2-Cl BP,soil organic matter（SOM）,especially the soft carbon,also served as an electron transfer medium to promote the dechlorination of 2-Cl BP in the long term.
基金the National Natural Science Foundation of China (Grant No. 20537020)
文摘Nanosized zero-valent iron (NZVI) supported on the cation exchange resin was synthesized and applied to decompose some water soluble azo dyes. The decomposition efficiency for azo dyes was evaluated by using the aqueous suspensions and parked column of this material. Batch experiments indicated that this novel material exhibited excellent degradation ability for 0.05 g·L1 of Acid Orange 7, Acid Orange 8, Acid Orange 10, Sunset Yellow, and Methyl Orange, with decolorization ratio up to 95% in 4 min; pH value was the key factor for degradation and H+ was one of the reactants; adsorption of azo dyes onto the material existed at the beginning but reduced gradually until disappearing completely. For the packed column system, 58%~90% of azo dyes were decomposed in the 1st circle of solution passing through the column, and the adsorption onto the materials could accelerate the degradation azo dyes with the increasing reaction time. During the degradation process, Fe2+, the product of NZVI, was exchanged to the resin again and could be reduced to Fe0 by KBH4 for reusing. The 10th refreshed NZVI possessed reductive activity up to 90% of the newly systhesized NZVI. Decomposing pollutants in the aqueous solution with columns packed with NZVI immobilized on the cation exchange resin is a promising technology that can solve the reclaiming and refreshing problem of NZVI.
基金supported by the National Natural Science Foundation of China (No.21477133)the Key Lab of Photovoltaic and Energy Conservation Materials,Chinese Academy of Sciences is acknowledged
文摘Nanoscale zerovalent iron/magnetic carbon(NZVI/MC) composites were successfully synthesized by simply calcining yellow pine and iron precursors. NZVI/MC pyrolyzed at 800°C(NZVI/MC800) had a higher percentage of NZVI and displayed better resistance to aggregation and oxidation of NZVI than samples prepared at other temperatures. The NZVI/MC800 material was applied for the elimination of U(Ⅵ) from aqueous solutions. The results suggested that the NZVI/MC800 displayed excellent adsorption capacity(203.94 mg/g)toward U(Ⅵ). The significant adsorption capacity and fast adsorption kinetics were attributed to the presence of well-dispersed NZVI, which could quickly reduce U(Ⅵ) into U(Ⅳ), trapping the guest U(Ⅳ) in the porous biocarbon matrix. The removal of U(Ⅵ) on the NZVI/MC samples was strongly affected by solution pH. The NZVI/MC samples also displayed outstanding reusability for U(Ⅵ) removal after multiple cycles. These findings indicate that NZVI/MC has great potential for remediation of wastewater containing U(Ⅵ).
文摘Nano zero valent iron particles (nZVI) are popular the last few years because of the numerous applications in remediation of a wide range of pollutants in contaminated soils and aquifers. The nZVI particles can be 10 - 1000 times more reactive than granular or micro-scale ZVI particles due to the small particle size, large specific surface area and high reactivity. An alternative green synthesis procedure was used for the production of nano zero valent iron particles (nZVI) using green tea (GT) extract, which is characterized by its high antioxidant content. Polyphenols in green tea extract possess double role in the synthesis of nZVI, because they not only reduce ferric cations, but also protect nZVI from oxidation and agglomeration as capping agents. The objective of current study was to simulate ata laboratory scale the attachment of GT-nZVI particles on soil material and study the effectiveness of attached nanoparticles for removing hexavalent chromium (Cr(VI)) from contaminated groundwater flowing through the porous soil bed. Column tests were carried out with various flowrates in order to examine the effect of contact time between the attached on porous medium nZVI and the flow-through solution on Cr(VI) reduction. After the completion of column tests the soil material in each column was split in 5 vertical sections, which were further subjected to chemical analyses and leaching tests. According to the results of the study increasing the contact time favors the reduction and removal of Cr(VI) from the aqueous phase. The reductive precipitation of Cr can be described as a reaction that follows a pseudo-first order kinetic law, with rate constant equal to k = 0.0243 ± 0.0011 min-1. Leaching tests indicated that precipitated chromium is not soluble. In the examined soil material, the total amount of precipitated Cr was found to range between 280 and 890 mg/(kg soil), while soluble Cr was less than 1.4 mg/kg and most probably it was due to the presence of residual Cr(VI) solution in the porosity of soil.
基金This work was financially supported by the National Natural Science Foundation of China(51978488,41772243 and 41673096).
文摘Nitrate is the leading cause of eutrophication worldwide and is one of the most challenging pollutants for restoration of polluted surface waters such as lakes, rivers and reservoirs. We report herein a new architecture of iron nanoparticles for high-efficiency denitrification by selective reduction of nitrate (NO3-) to dinitrogen (N2). The iron nanoparticles are doped with nitrogen (FeN) and encapsulated within a thin layer of nitride-carbon (NC). The nanoparticles have high pyrrolic N content (17.4 at.%) and large specific surface area (2040 m2/g). Laboratory experiments demonstrated high N2selectivity (91%) and nitrate removal capacity (6004 mg N/g Fe) for treatment of nitrate-containing water. This iron-based nanomaterial overcomes shortcomings of conventional catalysts by eliminating the use of precious and toxic heavy metals (e.g., Pd, Pt, Cu, Ni) and minimizing the generation of undesirable byproducts (e.g., ammonia) from the reactions with nanoscale zero-valent iron (n ZVI). The multiple electron transfers process from NO3- to N2can be fine-tuned by adjusting the NC shell thickness. Superior electrocatalytic perfor- mance, low cost and minimal environmental impact of the iron-derived nanocatalyst offer promising prospects for water purification, waste treatment and environmental remediation.
