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.

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 Synthesis of Iron Doped Zeolite Imidazolate Framework-8 and Its Remazol Deep Black RGB Dye Adsorption Ability

2017 ◽  
Vol 2017 ◽  
pp. 1-18 ◽  
Author(s):  
Mai Thi Thanh ◽  
Tran Vinh Thien ◽  
Vo Thi Thanh Chau ◽  
Pham Dinh Du ◽  
Nguyen Phi Hung ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Hydrothermal Process ◽  
Dye Adsorption ◽  
Specific Area ◽  
Nitrogen Adsorption ◽  
Vital Role ◽  
Factors Affecting ◽  
X Ray ◽  
Effective Removal ◽  
Iron Doped

Zeolite imidazole framework-8 (ZIF-8) and the iron doped ZIF-8 (Fe-ZIF-8) were synthesized by the hydrothermal process. The obtained materials were characteristic of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), nitrogen adsorption/desorption isotherms, and atomic absorption spectroscopy (AAS). The results showed that the obtained Fe-ZIF-8 possessed the ZIF-8 structure with a large specific area. ZIF-8 and Fe-ZIF-8 were used for the removal of Remazol Deep Black (RDB) RGB dye from aqueous solutions. The various factors affecting adsorption such as pH, initial concentration, contact time, and temperature were investigated. The results showed that the introduction of iron into ZIF-8 provided a much larger adsorption capacity and faster adsorption kinetics than ZIF-8 without iron. The electrostatic interaction and π-π interaction between the aromatic rings of the RDB dye and the aromatic imidazolate rings of the adsorbent were responsible for the RDB adsorption. Moreover, the coordination of the nitrogen atoms and oxygen in carboxyl group in RDB molecules with the Fe2+ ions in the ZIF-8 framework played a vital role for the effective removal of RDB from aqueous solution.

scholarly journals CoMn2O4 Catalyst Prepared Using the Sol-Gel Method for the Activation of Peroxymonosulfate and Degradation of UV Filter 2-Phenylbenzimidazole-5-sulfonic Acid (PBSA)

Nanomaterials ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 774 ◽  
Author(s):  
Chihao Lin ◽  
Dejian Shi ◽  
Zhentao Wu ◽  
Lingfeng Zhang ◽  
Zhicai Zhai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Sulfonic Acid ◽  
Sol Gel ◽  
Nitrogen Adsorption ◽  
Paramagnetic Resonance ◽  
Uv Filter ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method

In this study, a bimetallic oxide catalyst of cobalt-manganese (CoMn2O4) was synthesized using the sol-gel method, and it was then characterized using a variety of techniques such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) spectroscopy, X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption–desorption isotherms. The obtained novel catalyst, i.e., CoMn2O4, was then used as an activator of peroxymonosulfate (PMS) for the catalytic degradation of a commonly-used UV filter, 2-phenylbenzimidazole-5-sulfonic acid (PBSA) in water. The effects of various factors (e.g., catalyst dosage, PMS concentration, reaction temperature, and pH) in the process were also evaluated. Chemical scavengers and electron paramagnetic resonance (EPR) tests showed that the •OH and SO4•− were the main reactive oxygen species. Furthermore, this study showed that CoMn2O4 is a promising catalyst for activating PMS to degrade the UV filters.

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.

scholarly journals Effective TiO2-Sulfonated Carbon-derived from Eichhornia crassipes in The Removal of Methylene Blue and Congo Red Dyes from Aqueous Solution

2020 ◽  
Vol 15 (2) ◽  
pp. 476-489
Author(s):  
Iis Intan Widiyowati ◽  
Mukhamad Nurhadi ◽  
Muhammad Hatami ◽  
Lai Sin Yuan
Keyword(s):  
Aqueous Solution ◽  
Methylene Blue ◽  
Congo Red ◽  
Contact Time ◽  
Eichhornia Crassipes ◽  
Dye Removal ◽  
Nitrogen Adsorption ◽  
Order Kinetic ◽  
X Ray ◽  
Removal Capacity

The study of TiO2-sulfonated carbon-derived from Eichhornia crassipes (TiO2/SCEC), as an effective adsorbent to remove Methylene blue (MB) and Congo red (CR) dyes from aqueous solution, has been conducted. The preparation steps of TiO2/SCEC adsorbent involved the carbonisation of E. crassipes powder at 600 °C for 1 h, followed by sulfonation of carbon for 3 h and impregnation through titanium(IV) isopropoxide (500 µmol). The physical properties of the adsorbents were characterized by using X-ray fluorescence (XRF), Fourier transform infrared, X-ray diffraction (XRD), Scanning electron microscopy with Energy dispersive X-ray (SEM-EDX), Thermogravimetric analysis (TGA) and nitrogen adsorption-desorption studies. The dye removal study using TiO2/SCEC adsorbent was carried out by varying of contact time, adsorbent dosage, initial dye concentration, pH, particles size of adsorbent and temperature. The kinetics models were determined by the effects of contact time and the thermodynamic parameters (ΔH, ΔS, and ΔG), which were calculated by the effects of temperature. The results showed that the maximum dye removal capacity of TiO2/SCEC were 18.8 mg.g-1 for MB and 36.5 mg.g-1 for CR. The removal of MB and CR dyes using TiO2/SCEC adsorbent performed a pseudo-second order kinetic models with spontaneity. Copyright © 2020 BCREC Group. All rights reserved 

Jellyfish-like few-layer graphene nanoflakes: high paramagnetic response alongside increased interlayer interaction

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Alexander Ulyanov ◽  
Dmitrii Stolbov ◽  
Serguei Savilov
Keyword(s):  
Photoelectron Spectroscopy ◽  
High Sensitivity ◽  
Paramagnetic Centers ◽  
Interlayer Interaction ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Graphene Nanoflakes ◽  
Few Layer Graphene ◽  
Electron Paramagnetic ◽  
Hydrocarbon Pyrolysis

Abstract Jellyfish-like graphene nanoflakes (GNF), prepared by hydrocarbon pyrolysis, are studied with electron paramagnetic resonance (EPR) method. The results are supported by X-ray photoelectron spectroscopy (XPS) data. Oxidized (GNFox) and N-doped oxidized (N-GNFox) flakes exhibit an extremely high EPR response associated with a large interlayer interaction which is caused by the structure of nanoflakes and layer edges reached by oxygen. The GNFox and N-GNFox provide the localized and mobile paramagnetic centers which are silent in the pristine (GNF p ) and N-doped (N-GNF) samples. The change in the relative intensity of the line corresponding to delocalized electrons is parallel with the number of radicals in the quaternary N-group. The environment of localized and mobile electrons is different. The results can be important in GNF synthesis and for explanation of their features in applications, especially, in devices with high sensitivity to weak electromagnetic field.

scholarly journals Pore Modification and Phosphorus Doping Effect on Phosphoric Acid-Activated Fe-N-C for Alkaline Oxygen Reduction Reaction

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1519
Author(s):  
Jong Gyeong Kim ◽  
Sunghoon Han ◽  
Chanho Pak
Keyword(s):  
Phosphoric Acid ◽  
Photoelectron Spectroscopy ◽  
Structural Changes ◽  
Electronic States ◽  
Nitrogen Adsorption ◽  
Reduction Reaction ◽  
Phosphorus Doping ◽  
X Ray ◽  
Precious Metal Catalysts ◽  
Adsorption Desorption

The price and scarcity of platinum has driven up the demand for non-precious metal catalysts such as Fe-N-C. In this study, the effects of phosphoric acid (PA) activation and phosphorus doping were investigated using Fe-N-C catalysts prepared using SBA-15 as a sacrificial template. The physical and structural changes caused by the addition of PA were analyzed by nitrogen adsorption/desorption and X-ray diffraction. Analysis of the electronic states of Fe, N, and P were conducted by X-ray photoelectron spectroscopy. The amount and size of micropores varied depending on the PA content, with changes in pore structure observed using 0.066 g of PA. The electronic states of Fe and N did not change significantly after treatment with PA, and P was mainly found in states bonded to oxygen or carbon. When 0.135 g of PA was introduced per 1 g of silica, a catalytic activity which was increased slightly by 10 mV at −3 mA/cm2 was observed. A change in Fe-N-C stability was also observed through the introduction of PA.

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