Mechanism of Cu2+ Ions Removal from Aqueous Solution with PBTCA Modified Fe0 Nanoparticles

2014 ◽  
Vol 522-524 ◽  
pp. 454-457
Author(s):  
Jing Wei Feng ◽  
Ying Xia Xu
Keyword(s):  
Aqueous Solution ◽  
Iron Oxide ◽  
Photoelectron Spectroscopy ◽  
Aqueous Media ◽  
Zero Valent Iron ◽  
Borohydride Reduction ◽  
Experimental Conditions ◽  
Redox Mechanism ◽  
X Ray ◽  
Nanoscale Zero Valent Iron

Applications of PBTCA modified nanoscale zero valent iron (P-Fe0) prepared by borohydride reduction for removal of Cu2+ions from aqueous solution are investigated under a variety of experimental conditions. According to X-ray photoelectron spectroscopy (XPS) results, Cu2+ions were removed primarily via a redox mechanism that resulted in the formation of Cu0and Cu2O. The contact of P-Fe0with aqueous media caused extensive formation of iron oxide.

scholarly journals Simultaneous adsorption and reduction of hexavalent chromium on biochar-supported nanoscale zero-valent iron (nZVI) in aqueous solution

2020 ◽  
Vol 82 (7) ◽  
pp. 1339-1349
Author(s):  
Fengfeng Ma ◽  
Bakunzibake Philippe ◽  
Baowei Zhao ◽  
Jingru Diao ◽  
Jian Li
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Zero Valent Iron ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Nanoscale Zero Valent Iron ◽  
Pseudo Second Order

Abstract Flax straw biochar (FSBC)-supported nanoscale zero-valent iron (nZVI) composite (nZVI-FSBC) combining the advantages of nZVI and biochar was synthesized and tested for Cr(VI) removal efficiency from aqueous solution. Surface morphology and structure of FSBC and nZVI-FSBC were characterized by scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and Brunauer–Emmett–Teller techniques, which help to clarify the mechanism of Cr(VI) removal from aqueous solution. The adsorption of Cr(VI) onto FSBC and nZVI-FSBC was best described by the pseudo-second-order and the Sips model. Compared with FSBC, nZVI-FSBC remarkably improved the performance in removing Cr(VI) under identical experimental conditions. Due to the collaborative effect of adsorption and reduction of nZVI-FSBC, the adsorption capacity of nZVI-FSBC for Cr(VI) is up to 186.99 mg/g. The results obtained by XPS, XRD, and FTIR confirmed that adsorption and reduction dominated the processes of Cr(VI) removal by nZVI-FSBC. As a supporter, FSBC not only improved the dispersion of nZVI, but also undertook the adsorption task of Cr(VI) removal. The surface oxygen-containing functional groups of nZVI-FSBC mainly participated in the adsorption part, and the nZVI promoted the Cr(VI) removal through the redox reactions. These observations indicated that the nZVI-FSBC can be considered as potential adsorbents to remove Cr(VI) for environment remediation.

A Facile Strategy to Fabricate Nanoscale Zero-Valent Iron Decorated Graphene Oxide Composite for Dechloridation of Trichloroacetic Acid in Water

2018 ◽  
Vol 18 (12) ◽  
pp. 8252-8257 ◽  
Author(s):  
Huixuan Zhang ◽  
Xinyi Zhang ◽  
Ruonan Guo ◽  
Qingfeng Cheng ◽  
Xiuwen Cheng
Keyword(s):  
Graphene Oxide ◽  
Photoelectron Spectroscopy ◽  
Sewage Treatment ◽  
Reduction Process ◽  
Zero Valent Iron ◽  
Chlorinated Organic Compounds ◽  
X Ray ◽  
Transmission Electron ◽  
Nanoscale Zero Valent Iron ◽  
Adsorption Desorption

In this study, nanoscale zero-valent iron decorated graphene oxide (NZVI/GO) composite was fabricated through a reduction process in the presence of sodium borohydride (NaBH4) solution. Subsequently, physicochemical properties of the NZVI/GO composites were characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), N2 adsorption/desorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transformation infrared spectroscopy (FT-IR) and Raman spectra. Results indicated that Fe species existed in the form of Fe0, which uniformly dispersed on the surface of GO. Furthermore, the performance of NZVI/GO was evaluated by the degradation of tichloroacetic acid (TCAA). TCAA can be rapidly degraded by NZVI/GO. This paper provides a promising strategy to synthesize versatile catalyst which would be potentially applied in sewage treatment to degrade chlorinated organic compounds.

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 Removal efficiency of hexavalent chromium from wastewater using starch-stabilized nanoscale zero-valent iron

2019 ◽  
Vol 80 (6) ◽  
pp. 1076-1084 ◽  
Author(s):  
Hualin Chen ◽  
Huajun Xie ◽  
Jiangmin Zhou ◽  
Yueliang Tao ◽  
Yongpu Zhang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
High Reactivity ◽  
Zero Valent Iron ◽  
X Ray Diffraction ◽  
X Ray ◽  
Phase Reduction ◽  
Nanoscale Zero Valent Iron ◽  
Removal Efficiencies ◽  
Ph Range ◽  
Uniform Particle Size

Abstract In this study, starch-stabilized nanoscale zero-valent iron (S-nZVI) was produced using the liquid-phase reduction method. It was used to remove chromium from wastewater, and compared to a commercial nanoscale zero-valent iron (C-nZVI). Both nZVIs were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The characterization results showed that S-nZVI had smaller particles and a more uniform particle size distribution than C-nZVI. Both nZVIs showed a core-shell structure with the Fe0 core prominently surrounded by less iron oxides of Fe2+ and Fe3+. The optimal application methods to remove Cr(VI) from wastewater were also explored. The results showed that both the removal efficiencies of total Cr and Cr(VI) increased with increases in the addition of nZVIs, while the removal efficiencies of total Cr and Cr(VI) by S-nZVI were clearly higher than that of C-nZVI, especially in a low pH range (pH = 1.0–6.0). This research indicated that starch-stabilized nanoscale zero-valent iron is a valuable material to remove heavy metals from wastewater due to its stability and high reactivity.

scholarly journals Hydrothermal Enhanced Nanoscale Zero-Valent Iron Activated Peroxydisulfate Oxidation of Chloramphenicol in Aqueous Solutions: Fe-Speciation Analysis and Modeling Optimization

Water ◽  
2019 ◽  
Vol 12 (1) ◽  
pp. 131 ◽  
Author(s):  
Lie Yang ◽  
Hong Li ◽  
Jianming Xue ◽  
Liuyang He ◽  
Yongfei Ma ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Photoelectron Spectroscopy ◽  
Speciation Analysis ◽  
Zero Valent Iron ◽  
Quadratic Model ◽  
X Ray ◽  
Condition Optimization ◽  
Degradation Rates ◽  
Nanoscale Zero Valent Iron ◽  
Initial Ph

The efficiencies of the nanoscale zero-valent iron (nZVI) and hydrothermal and nZVI-heat activation of peroxydisulfate (PS) were studied for the decomposition of chloramphenicol (CAP) in aqueous solutions. The nZVI heat combined with activation of PS provided a significant synergistic effect. A central composite design (CCD) with response surface methodology (RSM) was employed to explore the influences of single parameter and interactions of selected variables (initial pH, PS concentration, nZVI and temperature) on degradation rates with the purpose of condition optimization. A quadratic model was established based on the experimental results with excellent correlation coefficients of 0.9908 and 0.9823 for R2 and R2adj. The optimized experimental condition for 97.12% CAP removal was predicted with the quadratic model as 15 mg/L, 0.5 mmol/L, 7.08 and 70 °C for nZVI dosage, PS, initial pH, and temperature, respectively. This study demonstrated the effectiveness of RSM for the modeling and prediction of CAP removal processes. In the optimal condition, Fe2O3 and Fe3O4 were the predominant solid products after reactions based on X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) analysis, which could also act as the activators along with the reaction. Overall, it could be concluded that hydrothermal enhanced nZVI activation of PS was a promising and efficient choice for CAP degradation.

scholarly journals Pyrolytic Formation of TiO2/Carbon Nanocomposite from Kraft Lignin: Characterization and Photoactivities

Catalysts ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 270
Author(s):  
Dhanalakshmi Vadivel ◽  
Diego Savio Branciforti ◽  
Andrea Speltini ◽  
Michela Sturini ◽  
Vittorio Bellani ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Uv Light ◽  
Tap Water ◽  
Aqueous Media ◽  
Pyrolytic Carbon ◽  
Kraft Lignin ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
Paramagnetic Resonance ◽  
X Ray

This article reports on the formation of pyrolytic carbon/TiO2 nanocomposite (p-C/TiO2) by pyrolysis of a mixture of the P25 TiO2 and kraft lignin at 600 °C. The result was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV-visible spectroscopy, electron paramagnetic resonance spectrometry (EPR), thermogravimetry (TGA) and SEM microscopy. Its photocatalytic activity was ascertained using three classes of chemical probes, namely (i) degradation of methylene blue (MB) and rhodamine-B (RhB) dyes in UV light-irradiated aqueous suspensions, (ii) depletion of phenol and (iii) degradation of antibiotics. The p-C/TiO2 nanocomposite is a strong phisisorbent of both MB and RhB nearly twofold with respect to neat TiO2. Although it is nearly twofold more photoactive toward the degradation of MB (0.091 min−1 versus 0.047 min−1), it is not with regard to RhB degradation (0.064 min−1 versus 0.060 min−1). For the degradation of phenol in aqueous media (pH 3), pristine TiO2 was far more effective than p-C/TiO2 for oxygenated suspensions (17.6 × 10−3 mM min−1 versus 4.3 × 10−3 mM min−1). Under an argon atmosphere, the kinetics were otherwise identical. The activity of the material was tested also for a real application in the degradation of a fluoroquinolone antibiotic such as enrofloxacin (ENR) in tap water. It is evident that the photoactivity of a semiconductor photocatalyst is not a constant, but it does depend on the nature of the substrate used and on the experimental conditions. It is also argued that the use of dyes to assess photocatalytic activities when suspensions are subjected to visible light irradiation is to be discouraged as the dyes act as electron transfer photosensitizers and or can undergo photodegradation from their excited states.

scholarly journals Removal of trace mercury (II) from aqueous solution by in situ MnOx combined with poly-aluminum chloride

2014 ◽  
Vol 13 (2) ◽  
pp. 383-393 ◽  
Author(s):  
Xixin Lu ◽  
Xiaoliu Huangfu ◽  
Xiang Zhang ◽  
Yaan Wang ◽  
Jun Ma
Keyword(s):  
Water Quality ◽  
Aqueous Solution ◽  
Mercury Concentration ◽  
Aluminum Chloride ◽  
Photoelectron Spectroscopy ◽  
Active Sites ◽  
Mercury Removal ◽  
Experimental Conditions ◽  
X Ray

Removal of trace mercury from aqueous solution by Mn (hydr)oxides formed in situ during coagulation with poly-aluminum chloride (PAC) (in situ MnOx combined with PAC) was investigated. The efficiency of trace mercury removal was evaluated under the experimental conditions of reaction time, Mn dosage, pH, and temperature. In addition, the ionic strength and the initial mercury concentration were examined to evaluate trace mercury removal for different water qualities. The results clearly demonstrated that in situ MnOx combined with PAC was effective for trace mercury removal from aqueous solution. A mercury removal ratio of 9.7 μg Hg/mg Mn was obtained at pH 3. Furthermore, at an initial mercury concentration of 30 μg/L and pH levels of both 3 and 5, a Mn dosage of 4 mg/L was able to lower the mercury concentration to meet the standards for drinking water quality at less than 1 μg/L. Analysis by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy suggests that the hydroxyls on the surface of Mn (hydr)oxides are the active sites for adsorption of trace mercury from aqueous solution.

scholarly journals Acid Red 66 Dye Removal from Aqueous Solution by Fe/C-based Composites: Adsorption, Kinetics and Thermodynamic Studies

Materials ◽  
2020 ◽  
Vol 13 (5) ◽  
pp. 1107 ◽  
Author(s):  
Camila B. Paz ◽  
Rinaldo S. Araújo ◽  
Lais F. Oton ◽  
Alcineia C. Oliveira ◽  
João M. Soares ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Dye Removal ◽  
Dye Adsorption ◽  
Nitrogen Adsorption ◽  
Carbon Layer ◽  
Synthetic Dyes ◽  
Experimental Conditions ◽  
Paramagnetic Resonance ◽  
X Ray

The presence of synthetic dyes in water causes serious environmental issues owing to the low water quality, toxicity to environment and human carcinogenic effects. Adsorption has emerged as simple and environmental benign processes for wastewater treatment. This work reports the use of porous Fe-based composites as adsorbents for Acid Red 66 dye removal in an aqueous solution. The porous FeC and Fe/FeC solids were prepared by hydrothermal methods using iron sulfates and sucrose as precursors. The physicochemical properties of the solids were evaluated through X-ray diffraction (XRD), Scanning electron microscopy coupled with Energy dispersive spectroscopy (SEM-EDS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared s (FTIR), Raman and Mössbauer spectroscopies, nitrogen adsorption–desorption isotherms, Electron Paramagnetic Resonance (EPR) and magnetic saturation techniques. Results indicated that the Fe species holds magnetic properties and formed well dispersed Fe3O4 nanoparticles on a carbon layer in FeC nanocomposite. Adding iron to the previous solid resulted in the formation of γ-Fe2O3 coating on the FeC type structure as in Fe/FeC composite. The highest dye adsorption capacity was 15.5 mg·g−1 for FeC nanocomposite at 25 °C with the isotherms fitting well with the Langmuir model. The removal efficiency of 98.4% was obtained with a pristine Fe sample under similar experimental conditions.

A low cost synthesis method for functionalised iron oxide nanoparticles for magnetic hyperthermia from readily available materials

2014 ◽  
Vol 175 ◽  
pp. 83-95 ◽  
Author(s):  
Joseph C. Bear ◽  
Bin Yu ◽  
Cristina Blanco-Andujar ◽  
Paul D. McNaughter ◽  
Paul Southern ◽  
...  
Keyword(s):  
Iron Oxide ◽  
Photoelectron Spectroscopy ◽  
Low Cost ◽  
Aqueous Media ◽  
Synthesis Method ◽  
Magnetic Hyperthermia ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Street ◽  
Fatty Acid Precursor

The synthesis of iron oxide nanocrystals from reagents taken from high street sources using thermal decomposition of an iron–fatty acid precursor in a high boiling point solvent in the presence of surfactants is presented. The nanocrystals were characterised using a variety of techniques including: electron microscopy, X-ray dispersive spectroscopy, infrared spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and magnetometry. Thermogravimetric analysis (TGA) is also used to compare the decomposition behaviour of iron oleate and iron palmitate, our nanoparticle precursors. The nanoparticles also exhibit shape anisotropy when prepared under optimum conditions. We show that these nanoparticles have potential in magnetic hyperthermia after transfer to aqueous media via an amphiphilic polymer.

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