Novel composite sorbents based on carbon fibers decorated with ferric hydroxides – simultaneous removal of antimonate and arsenate from aqueous solutions

Abstract The competitive adsorption of antimonate and arsenate on carbon fibers decorated with ferric hydroxide (CF-Fe) has been investigated at different pH and temperatures. Tap and drinking water samples spiked with unitary and binary solutions were subjected to kinetic tests and compared with distilled water media. As the required time for attaining the arsenate concentration permitted by law, the legal limit was found as 3 hours for drinking and tap water systems. It was shown that arsenate can be adsorbed more strongly than antimonate. Such multiple adsorption/desorption cycles showed that the CF-Fe sample had approximately 96% of the first antimonate adsorption at the seventh cycle. X-ray photoelectron spectroscopy (XPS) analyses were performed in order to obtain insight into the adsorption mechanism.

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Preparation of GO/MIL-101(Fe,Cu) composite and its adsorption mechanisms for phosphate in aqueous solution

10.21203/rs.3.rs-191207/v1 ◽

2021 ◽

Author(s):

You Wu ◽

Zuannian Liu ◽

Bakhtari Mohammad Fahim ◽

Junnan Luo

Keyword(s):

Adsorption Capacity ◽

Photoelectron Spectroscopy ◽

Adsorption Mechanism ◽

Nitrogen Adsorption ◽

Adsorption Properties ◽

Maximum Adsorption Capacity ◽

X Ray Diffraction ◽

X Ray ◽

Adsorption Mechanisms ◽

Adsorption Desorption

Abstract In this study, MIL-101(Fe), MIL-101(Fe,Cu), and Graphene Oxide (GO) /MIL-101(Fe,Cu) were synthesized to compose a novel sorbent. The adsorption properties of these three MOFs-based composites were compared toward the removal of phosphate. Furthermore, the influencing factors including reaction time, pH, temperature and initial concentration on the adsorption capacity of phosphate on these materials as well as the reusability of the material were discussed. The structure of fabricated materials and the removal mechanism of phosphate on the composite material were analyzed by Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption-desorption analysis and zeta potential. The results show that the maximum adsorption capacity of phosphate by the composite GO/MIL-101(Fe,Cu)-2% was 204.60 mg·g− 1, which is higher than that of MIL-101(Fe,Cu) and MIL-101(Fe). likewise the specific surface area of GO/MIL-101(Fe,Cu)-2% is 778.11 m2/g is higher than that of MIL-101(Fe,Cu) and MIL-101(Fe),which are 747.75 and 510.66m2/g respectively. The adsorption mechanism of phosphate is electrostatic attraction, form coordination bonds and hydrogen bonds. The fabricated material is a promising adsorbent for the removal of phosphate with good reusability.

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Carboxin and Diuron Adsorption Mechanism on Sunflower Husks Biochar and Goethite in the Single/Mixed Pesticide Solutions

Materials ◽

10.3390/ma14102584 ◽

2021 ◽

Vol 14 (10) ◽

pp. 2584

Author(s):

Katarzyna Szewczuk-Karpisz ◽

Agnieszka Tomczyk ◽

Magdalena Celińska ◽

Zofia Sokołowska ◽

Marcin Kuśmierz

Keyword(s):

Photoelectron Spectroscopy ◽

Adsorption Mechanism ◽

Nitrogen Adsorption ◽

Theoretical Models ◽

Second Order ◽

Adsorption Data ◽

Pseudo Second Order ◽

Adsorption Desorption ◽

Mixed Systems ◽

Second Order Equations

The study focused on the adsorption mechanism of two selected pesticides: carboxin and diuron, on goethite and biochar, which were treated as potential compounds of mixed adsorbent. The authors also prepared a simple mixture of goethite and biochar and performed adsorption measurements on this material. The adsorbents were characterized by several methods, inter alia, nitrogen adsorption/desorption, Boehm titration, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The adsorption study included kinetics and equilibrium measurements, in the solution containing one or two pesticides simultaneously. The adsorption data were fitted to selected theoretical models (e.g., Langmuir, Freudlich, Redlich–Peterson, pseudo first-order and pseudo second-order equations). Based on the obtained results, it was stated that, among all tested adsorbents, biochar had the highest adsorption capacity relative to both carboxin and diuron. It equaled 0.64 and 0.52 mg/g, respectively. Experimental data were best fitted to the pseudo second-order and Redlich–Peterson models. In the mixed systems, the adsorption levels observed on biochar, goethite and their mixture were higher for diuron and lower for carboxin, compared to those noted in the single solutions. The presented results may enable the development of new mixed adsorbent for remediation of soils polluted with pesticides.

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Insight into Active Centers and Anti-Coke Behavior of Niobium-Containing SBA-15 for Glycerol Dehydration

Catalysts ◽

10.3390/catal11040488 ◽

2021 ◽

Vol 11 (4) ◽

pp. 488

Author(s):

Katarzyna Stawicka ◽

Maciej Trejda ◽

Maria Ziolek

Keyword(s):

Coke Formation ◽

Catalytic Performance ◽

Acid Sites ◽

Silica Matrix ◽

High Concentration ◽

Active Centers ◽

Acidic Sites ◽

Glycerol Dehydration ◽

Adsorption Desorption ◽

Insight Into

Niobium containing SBA-15 was prepared by two methods: impregnation with different amounts of ammonium niobate(V) oxalate (Nb-15/SBA-15 and Nb-25/SBA-15 containing 15 wt.% and 25 wt.% of Nb, respectively) and mixing of mesoporous silica with Nb2O5 followed by heating at 500 °C (Nb2O5/SBA-15). The use of these two procedures allowed obtaining materials with different textural/surface properties determined by N2 adsorption/desorption isotherms, XRD, UV-Vis, pyridine, and NO adsorption combined with FTIR spectroscopy. Nb2O5/SBA-15 contained exclusively crystalline Nb2O5 on the SBA-15 surface, whereas the materials prepared by impregnation had both metal oxide and niobium incorporated into the silica matrix. The niobium species localized in silica framework generated Brønsted (BAS) and Lewis (LAS) acid sites. The inclusion of niobium into SBA-15 skeleton was crucial for the achievement of high catalytic performance. The strongest BAS were on Nb-25/SBA-15, whereas the highest concentration of BAS and LAS was on Nb-15/SBA-15 surface. Nb2O5/SBA-15 material possessed only weak LAS and BAS. The presence of the strongest BAS (Nb-25/SBA-15) resulted in the highest dehydration activity, whereas a high concentration of BAS was unfavorable. Silylation of niobium catalysts prepared by impregnation reduced the number of acidic sites and significantly increased acrolein yield and selectivity (from ca. 43% selectivity for Nb-25/SBA-15 to ca. 61% for silylated sample). This was accompanied by a considerable decrease in coke formation (from 47% selectivity for Nb-25/SBA-15 to 27% for silylated material).

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

Nanomaterials ◽

10.3390/nano11061519 ◽

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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Crayfish shell-based micro-mesoporous activated carbon: Insight into preparation and gaseous benzene adsorption mechanism

Chemical Engineering Journal ◽

10.1016/j.cej.2021.131148 ◽

2021 ◽

pp. 131148

Author(s):

Guibin Shi ◽

Song He ◽

Guanyu Chen ◽

Chichi Ruan ◽

Yuansheng Ma ◽

...

Keyword(s):

Activated Carbon ◽

Adsorption Mechanism ◽

Benzene Adsorption ◽

Mesoporous Activated Carbon ◽

Gaseous Benzene ◽

Insight Into

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X-ray photoemission studies of the interaction of metals and metal ions with DNA

Zeitschrift für Physikalische Chemie ◽

10.1515/zpch-2021-3037 ◽

2021 ◽

Vol 0 (0) ◽

Author(s):

Esha Mishra ◽

Subrata Majumder ◽

Shikha Varma ◽

Peter A. Dowben

Keyword(s):

Heavy Metal ◽

Metal Ions ◽

Conformational Changes ◽

Photoelectron Spectroscopy ◽

X Ray ◽

Surface Sensitivity ◽

Metal Interaction ◽

The Status ◽

Sensitivity And Selectivity ◽

Insight Into

Abstract X-ray Photoelectron Spectroscopy (XPS) has been used to study the interactions of heavy metal ions with DNA with some success. Surface sensitivity and selectivity of XPS are advantageous for identifying and characterizing the chemical and elemental structure of the DNA to metal interaction. This review summarizes the status of what amounts to a large part of the photoemission investigations of biomolecule interactions with metals and offers insight into the mechanism for heavy metal-bio interface interactions. Specifically, it is seen that metal interaction with DNA results in conformational changes in the DNA structure.

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FeYO3@rGO nanocomposites: Synthesis, characterization and application in photooxidative degradation of atrazine under visible light

Materials Express ◽

10.1166/mex.2021.1957 ◽

2021 ◽

Vol 11 (5) ◽

pp. 706-716

Author(s):

Nada D. Al-Khthami ◽

Tariq Altalhi ◽

Mohammed Alsawat ◽

Mohamed S. Amin ◽

Yousef G. Alghamdi ◽

...

Keyword(s):

Visible Light ◽

Photoelectron Spectroscopy ◽

Sol Gel ◽

Bandgap Energy ◽

X Ray Diffraction ◽

X Ray ◽

Transmission Electron ◽

Reduced Graphene ◽

Structural Surface ◽

Adsorption Desorption

Different organic pollutants have been remediated photo catalytically by applying perovskite photocatalysts. Atrazine (ATR) is a pesticide commonly detected as a pollutant in drinking, surface and ground water. Herein, FeYO3@rGO heterojunction was synthesized and applied for photooxidation decomposition of ATR. First, FeYO 3nanoparticles (NPs) were prepared via routine sol-gel. After that, FeYO3 NPs were successfully incorporated with different percentages (5, 10, 15 and 20 wt.%) of reduced graphene oxide (rGO) in the synthesis of novel FeYO3@rGO photocatalyst. Morphological, structural, surface, optoelectrical and optical characteristics of constructed materials were identified via X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Transmission electron microscopy (TEM), adsorption/desorption isotherms, diffusive reflectance (DR) spectra, and photoluminescence response (PL). Furthermore, photocatalytic achievement of the constructed materials was evaluated via photooxidative degradation of ATR. Various investigations affirmed the usefulness of rGO incorporation on the advancement of formed photocatalysts. Actually, novel nanocomposite containing rGO (15 wt.%) possessed diminished bandgap energy, as well as magnified visible light absorption. Furthermore, such nanocomposite presented exceptional photocatalytic achievement when exposed to visible light as ATR was perfectly photooxidized over finite amount (1.6 g · L-1) from the optimized photocatalyst when illuminated for 30 min. The advanced photocatalytic performance of constructed heterojunctions could be accredited mainly to depressed recombination amid induced charges. The constructed FeYO3@rGO nanocomposite is labelled as efficient photocatalyst for remediation of herbicides from aquatic environments.

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Performance Evaluation of Small Sized Powdered Ferric Hydroxide as Arsenic Adsorbent

Water ◽

10.3390/w10070957 ◽

2018 ◽

Vol 10 (7) ◽

pp. 957 ◽

Cited By ~ 11

Author(s):

Muhammad Usman ◽

Ioannis Katsoyiannis ◽

Manassis Mitrakas ◽

Anastasios Zouboulis ◽

Mathias Ernst

Keyword(s):

Adsorption Capacity ◽

Tap Water ◽

Ferric Hydroxide ◽

Equilibrium Concentration ◽

Arsenic Species ◽

Batch Adsorption ◽

Order Kinetic ◽

Isothermal Adsorption ◽

Water Matrix ◽

The Impact

The small sized powdered ferric oxy-hydroxide, termed Dust Ferric Hydroxide (DFH), was applied in batch adsorption experiments to remove arsenic species from water. The DFH was characterized in terms of zero point charge, zeta potential, surface charge density, particle size and moisture content. Batch adsorption isotherm experiments indicated that the Freundlich model described the isothermal adsorption behavior of arsenic species notably well. The results indicated that the adsorption capacity of DFH in deionized ultrapure water, applying a residual equilibrium concentration of 10 µg/L at the equilibrium pH value of 7.9 ± 0.1, with a contact time of 96 h (i.e., Q10), was 6.9 and 3.5 µg/mg for As(V) and As(III), respectively, whereas the measured adsorption capacity of the conventionally used Granular Ferric Hydroxide (GFH), under similar conditions, was found to be 2.1 and 1.4 µg/mg for As(V) and As(III), respectively. Furthermore, the adsorption of arsenic species onto DFH in a Hamburg tap water matrix, as well as in an NSF challenge water matrix, was found to be significantly lower. The lowest recorded adsorption capacity at the same equilibrium concentration was 3.2 µg As(V)/mg and 1.1 µg As(III)/mg for the NSF water. Batch adsorption kinetics experiments were also conducted to study the impact of a water matrix on the behavior of removal kinetics for As(V) and As(III) species by DFH, and the respective data were best fitted to the second order kinetic model. The outcomes of this study confirm that the small sized iron oxide-based material, being a by-product of the production process of GFH adsorbent, has significant potential to be used for the adsorptive removal of arsenic species from water, especially when this material can be combined with the subsequent application of low-pressure membrane filtration/separation in a hybrid water treatment process.

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

Journal of Nanoscience and Nanotechnology ◽

10.1166/jnn.2018.16374 ◽

2018 ◽

Vol 18 (12) ◽

pp. 8252-8257 ◽

Cited By ~ 1

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.

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