scholarly journals Lanthanum-doped activated carbon derived from municipal sludge for enhanced defluoridation: characteristics and mechanism

2020 ◽  
Vol 82 (8) ◽  
pp. 1643-1652
Author(s):  
Lizhi He ◽  
Guoqiao Wang ◽  
Xinxin Zhang ◽  
Yujian Zhang ◽  
Yao Chen
Keyword(s):  
Activated Carbon ◽  
Photoelectron Spectroscopy ◽  
Removal Rate ◽  
Chemical Activation ◽  
Fluoride Concentration ◽  
Stability Study ◽  
Fluoride Removal ◽  
Municipal Sludge ◽  
Treatment Rate ◽  
X Ray

Abstract The sewage sludge production has been increasing along with the ever-growing populations and wastewater treatment rate. Lanthanum-doped activated carbon (AC-La) was derived from municipal sludge via chemical activation and utilized for fluoride removal. Batch experiments were conducted to discuss the effect of lanthanum dosage, time and pH on the adsorption process. The results showed that 4 g/L AC-La exhibited a fluoride removal rate of 80.9% with 10 mg/L initial fluoride concentration, and the optimal pH range for adsorption was 3–10. X-ray fluorescence, scanning electron microscopy with energy-dispersive X-ray spectroscopy, Brunauer-Emmett-Teller, X-ray diffraction, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses were conducted to analyze the microstructure and chemical properties of sludge, unmodified activated carbon (AC) and AC-La. The results showed that with initial lanthanum dosage of 15 wt%, the final loading amount of La in AC-La was 13.8 wt%. After modification, the specific surface area of AC-La increased from 1.8 m2/g (sludge) to 133.0 m2/g. The removal mechanism of fluoride onto AC-La was mainly the inner-sphere complexation between lanthanum and fluoride, facilitated by exchange interaction with hydroxyls. A stability study showed that AC-La maintained a quite small dissolution and was safe in waters (La dissolution rate < 0.2‰).

scholarly journals Synthesis and Characterization of Activated Carbon Co-Mixed Electrospun Titanium Oxide Nanofibers as Flow Electrode in Capacitive Deionization

Materials ◽  
2021 ◽  
Vol 14 (22) ◽  
pp. 6891
Author(s):  
Gbenro Folaranmi ◽  
Myriam Tauk ◽  
Mikhael Bechelany ◽  
Philippe Sistat ◽  
Marc Cretin ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Titanium Oxide ◽  
Photoelectron Spectroscopy ◽  
Removal Rate ◽  
Electrospinning Process ◽  
Water Desalination ◽  
Capacitive Deionization ◽  
Interfacial Resistance ◽  
X Ray ◽  
Electrode Passivation

Flow capacitive deionization is a water desalination technique that uses liquid carbon-based electrodes to recover fresh water from brackish or seawater. This is a potential second-generation water desalination process, however it is limited by parameters such as feed electrode conductivity, interfacial resistance, viscosity, and so on. In this study, titanium oxide nanofibers (TiO2NF) were manufactured using an electrospinning process and then blended with commercial activated carbon (AC) to create a well distributed flow electrode in this study. Field emission scanning electron microscope (FESEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and energy dispersive X-ray (EDX) were used to characterize the morphology, crystal structure, and chemical moieties of the as-synthesized composites. Notably, the flow electrode containing 1 wt.% TiO2NF (ACTiO2NF 1 wt.%) had the highest capacitance and the best salt removal rate (0.033 mg/min·cm2) of all the composites. The improvement in cell performance at this ratio indicates that the nanofibers are uniformly distributed over the electrode’s surface, preventing electrode passivation, and nanofiber agglomeration, which could impede ion flow to the electrode’s pores. This research suggests that the physical mixture could be used as a flow electrode in capacitive deionization.

scholarly journals Modified Activation Process for Supercapacitor Electrode Materials from African Maize Cob

Materials ◽  
2020 ◽  
Vol 13 (23) ◽  
pp. 5412
Author(s):  
Moses Kigozi ◽  
Ravi Kali ◽  
Abdulhakeem Bello ◽  
Balaji Padya ◽  
Godwin Mong Kalu-Uka ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Photoelectron Spectroscopy ◽  
Electrode Materials ◽  
Chemical Activation ◽  
Mesoporous Structure ◽  
Activation Process ◽  
Energy Storage Devices ◽  
Supercapacitor Electrode ◽  
X Ray ◽  
Bet Analysis

In this work, African maize cobs (AMC) were used as a rich biomass precursor to synthesize carbon material through a chemical activation process for application in electrochemical energy storage devices. The carbonization and activation were carried out with concentrated Sulphuric acid at three different temperatures of 600, 700 and 800 °C, respectively. The activated carbon exhibited excellent microporous and mesoporous structure with a specific surface area that ranges between 30 and 254 m2·g−1 as measured by BET analysis. The morphology and structure of the produced materials are analyzed through Field Emission Scanning Electron Microscopy (FESEM), Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD), Boehm titration, X-ray Photoelectron Spectroscopy (XPS) and Raman Spectroscopy. X-ray photoelectron spectroscopy indicates that a considerable amount of oxygen is present in the materials. The functional groups in the activated carbon enhanced the electrochemical performance and improved the material’s double-layer capacitance. The carbonized composite activated at 700 °C exhibited excellent capacitance of 456 F g−1 at a specific current of 0.25 A g−1 in 6 M KOH electrolyte and showed excellent stability after 10,000 cycles. Besides being a low cost, the produced materials offer good stability and electrochemical properties, making them suitable for supercapacitor applications.

scholarly journals Study on Adsorption Properties of Modified Corn Cob Activated Carbon for Mercury Ion

Energies ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4483
Author(s):  
Yuyingnan Liu ◽  
Xinrui Xu ◽  
Bin Qu ◽  
Xiaofeng Liu ◽  
Weiming Yi ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Photoelectron Spectroscopy ◽  
Adsorption Process ◽  
Physical Adsorption ◽  
Raw Material ◽  
Order Kinetic ◽  
Mercury Ions ◽  
Corn Cob ◽  
Adsorption Time ◽  
X Ray

In this study, corn cob was used as raw material and modified methods employing KOH and KMnO4 were used to prepare activated carbon with high adsorption capacity for mercury ions. Experiments on the effects of different influencing factors on the adsorption of mercury ions were undertaken. The results showed that when modified with KOH, the optimal adsorption time was 120 min, the optimum pH was 4; when modified with KMnO4, the optimal adsorption time was 60 min, the optimal pH was 3, and the optimal amount of adsorbent and the initial concentration were both 0.40 g/L and 100 mg/L under both modified conditions. The adsorption process conforms to the pseudo-second-order kinetic model and Langmuir model. Scanning electron microscopy and energy-dispersive X-ray spectroscopy (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and Zeta potential characterization results showed that the adsorption process is mainly physical adsorption, surface complexation and ion exchange.

Preparation of Novel Ag–Si–TiO2 Composite and Research on Its Photocatalytic Degradation of Formaldehyde

2021 ◽  
Vol 13 (3) ◽  
pp. 371-380
Author(s):  
Yongjun Wu ◽  
Nina Xie ◽  
Lu Yu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Removal Rate ◽  
Sol Gel ◽  
Catalytic Performance ◽  
Formaldehyde Concentration ◽  
Order Kinetic ◽  
Solution Ph ◽  
Visible Absorption ◽  
X Ray ◽  
Co Doped

A novel Ag–Si–TiO2 composite was prepared via sol–gel method for removing residual formaldehyde in shiitake mushroom. The structure of Ag–Si–TiO2 composite was characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses. Ultraviolet-visible absorption spectroscopy (UV-Vis) and N2 adsorption-desorption tests showed that Ag and Si co-doped decreased the band gap, the Brunauer-Emmett-Teller (BET) specific surface area of the samples increased and the recombination probability of electron-hole pairs (e--h+) reduced. Effect on removal rate of formaldehyde with different Ag-Si co-doped content, formaldehyde concentration and solution pH were investigated, and the results showed that 6.0 wt%Ag-3.0 wt%Si-TiO2 samples had an optimum catalytic performance, and the degradation efficiency reached 96.6% after 40 W 365 nm UV lamp irradiation for 360 min. The kinetics of formaldehyde degradation by Ag–Si–TiO2 composite photocatalyst could be described by Langmuir-Hinshelwood first-order kinetic model.

scholarly journals Characterisation of smectite-rich clay soil: Implication for groundwater defluoridation

2016 ◽  
Vol Volume 112 (Number 11/12) ◽  
Author(s):  
Rabelani Mudzielwana ◽  
Mugera W. Gitari ◽  
Titus A.M. Msagati ◽  
◽  
◽  
...  
Keyword(s):  
South Africa ◽  
Rural Areas ◽  
Contact Time ◽  
Clay Soil ◽  
Dental Fluorosis ◽  
Fluoride Concentration ◽  
Limpopo Province ◽  
World Health ◽  
Fluoride Removal ◽  
X Ray

Abstract Groundwater is a widely used and affordable source of drinking water in most of the rural areas of South Africa. Several studies have indicated that groundwater in some boreholes in South Africa has a fluoride concentration above the level recommended by the World Health Organization (1.5 mg/L). Fluoride concentrations above the permissible limit (>1.5 mg/L) lead to dental fluorosis, with even higher concentrations leading to skeletal fluorosis. In the present work, we evaluate the application of smectite-rich clay soil from Mukondeni (Limpopo Province, South Africa) in defluoridation of groundwater. The clay soil was characterised by mineralogy using X-ray diffraction, by elemental composition using X-ray fluorescence and by morphology using scanning electron microscopy. Surface area and pore volume was determined by the Brunauer–Emmett–Teller surface analysis method. Cation exchange capacity and pHpzc of the soil were also evaluated using standard laboratory methods. Batch experiments were conducted to evaluate and optimise various operational parameters such as contact time, adsorbent dose, pH and initial adsorbate concentration. It was observed that 0.8 g/100 mL of smectite-rich clay soil removed up to 92% of fluoride from the initial concentration of 3 mg/L at a pH of 2 with a contact time of 30 min. The experimental data fitted well to a Langmuir adsorption isotherm and followed pseudo second order reaction kinetics. Smectite-rich clay soil showed 52% fluoride removal from field groundwater with an initial fluoride concentration of 5.4 mg/L at an initial pH of 2 and 44% removal at a natural pH of 7.8. Therefore smectite-rich clay soil from Mukondeni has potential for application in defluoridation of groundwater. Chemical modification is recommended to improve the defluoridation capacity.

scholarly journals Biomass-Derived Activated Carbon as a Catalyst for the Effective Degradation of Rhodamine B dye

Processes ◽  
2020 ◽  
Vol 8 (8) ◽  
pp. 926
Author(s):  
Shamim Ahmed Hira ◽  
Mohammad Yusuf ◽  
Dicky Annas ◽  
Hu Shi Hui ◽  
Kang Hyun Park
Keyword(s):  
Electron Microscopy ◽  
Activated Carbon ◽  
Rhodamine B ◽  
Photoelectron Spectroscopy ◽  
High Specific Surface Area ◽  
High Porosity ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
X Ray ◽  
Transmission Electron

Activated carbon (AC) was fabricated from carrot waste using ZnCl2 as the activating agent and calcined at 700 °C for 2 h in a tube furnace. The as-synthesized AC was characterized using Fourier-transform infrared spectroscopy, X-ray diffraction analysis, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller analysis; the results revealed that it exhibited a high specific surface area and high porosity. Moreover, this material displayed superior catalytic activity for the degradation of toxic Rhodamine B (RhB) dye. Rate constant for the degradation of RhB was ascertained at different experimental conditions. Lastly, we used the Arrhenius equation and determined that the activation energy for the decomposition of RhB using AC was approximately 35.9 kJ mol−1, which was very low. Hopefully it will create a great platform for the degradation of other toxic dye in near future.

Laser Induced Decomposition of Triethylgallium and Trimethylgallium Adsorbed on GaAs(100)

1988 ◽  
Vol 129 ◽  
Author(s):  
J. A. Mccaulley ◽  
V. R. Mccrary ◽  
V. M. Donnelly
Keyword(s):  
Excimer Laser ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Electronic Excitation ◽  
Removal Rate ◽  
Laser Wavelength ◽  
High Fluence ◽  
X Ray ◽  
Two Photon ◽  
Induced Decomposition

ABSTRACTWe report X-ray photoelectron spectroscopy (XPS) studies of excimer laser stimulated decomposition of triethylgallium (TEGa) and trimethylgallium (TMGa) adsorbed on Gastabilized GaAs(100) surfaces in ultrahigh vacuum. TEGa and TMGa dissociatively chemisorb on GaAs at room temperature, whereupon irradiation by an excimer laser (at 193 or 351 nm) leads to further dissociation and desorption of carbon-containing species. The carbon removal rate (per laser pulse) decreases as carbon is removed suggesting multiple reaction sites, coverage dependent Arrhenius parameters, or second-order reactions. Based on the dependence of the rate on laser wavelength and fluence, we conclude that at low fluence, a two-photon electronic excitation of the adsorbate occurs, while at high fluence, laser induced pyrolysis dominates.

Improved Photocatalytic Activity of Copper Heterostructure Composites (Cu–Cu2O–CuO/AC) Prepared by Simple Carbothermal Reduction

2014 ◽  
Vol 67 (5) ◽  
pp. 749 ◽  
Author(s):  
Hongchao Ma ◽  
Yifeng Liu ◽  
Yinghuan Fu ◽  
Chunling Yu ◽  
Xiaoli Dong ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Photocatalytic Activity ◽  
Activated Carbon ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Carbothermal Reduction ◽  
Treatment Time ◽  
Carbon Support ◽  
Treatment Temperature ◽  
X Ray

Cu–Cu2O–CuO/activated carbon heterostructure composites with visible-light activity have been successfully synthesized by a simple carbothermal reduction procedure using CuSO4 as a single precursor. The resultant samples were characterized by X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy measurements. The results showed that the Cu–Cu2O–CuO composites with size less than 10 nm dispersed well on the surface of activated carbon. Activated carbon played both a reducing agent and support role in the formation of Cu–Cu2O–CuO/activated carbon heterostructure composites. X-ray photoelectron spectroscopy analysis suggests that the outside of the nanoparticles is CuO and the inside of the nanoparticles is Cu metal and Cu2O. Moreover, the composition of Cu–Cu2O–CuO/activated carbon composites can be tailored by varying the Cu loading, heat-treatment temperature, and heat-treatment time. The photocatalytic activities of the catalysts were investigated by degrading reactive brilliant blue KN-R under visible-light irradiation. The Cu–Cu2O–CuO/activated carbon heterostructure composites showed excellent photocatalytic activity compared with other catalysts (pure CuO, Cu2O, Cu2O/activated carbon, CuO/activated carbon, and Cu2O–CuO/activated carbon), which is ascribed to synergistic action between the activated carbon support and photoactive copper species, and the presence of interfacial structures such as a Cu2O/CuO heterostructure, Cu/Cu2O (or CuO) Schottky barrier, and Cu2O/Cu/CuO ohmic heterojunction.

scholarly journals Comparison of Surface and Structural Properties of Carbonaceous Materials Prepared by Chemical Activation of Tomato Paste Waste: The Effects of Activator Type and Impregnation Ratio

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Nurgul Ozbay ◽  
Adife Seyda Yargic
Keyword(s):  
Activated Carbon ◽  
Activated Carbons ◽  
Low Cost ◽  
Chemical Activation ◽  
Nitrogen Adsorption ◽  
Xrd Analysis ◽  
Point Of Zero Charge ◽  
Activation Process ◽  
X Ray ◽  
Tomato Paste

Activated carbons were prepared by carbonization of tomato paste processing industry waste at 500°C followed by chemical activation with KOH, K2CO3, and HCl in N2 atmosphere at low temperature (500°C). The effects of different activating agents and impregnation ratios (25, 50, and 100 wt.%) on the materials’ characteristics were examined. Precursor, carbonized tomato waste (CTW), and activated carbons were characterized by using ultimate and proximate analysis, thermogravimetric analysis (TG/DTG), Fourier transform-infrared (FT-IR) spectroscopy, X-ray fluorescence (XRF) spectroscopy, point of zero charge measurements (pHPZC), particle size analyzer, scanning electron microscopy (SEM), energy dispersive X-ray (EDX) spectroscopy, nitrogen adsorption/desorption isotherms, and X-ray diffraction (XRD) analysis. Activation process improved pore formation and changed activated carbons’ surface characteristics. Activated carbon with the highest surface area (283 m3/g) was prepared by using 50 wt.% KOH as an activator. According to the experimental results, tomato paste waste could be used as an alternative precursor to produce low-cost activated carbon.

scholarly journals An Experimental Study of Fluoride Removal from Wastewater by Mn-Ti Modified Zeolite

Water ◽  
2021 ◽  
Vol 13 (23) ◽  
pp. 3343
Author(s):  
Bo Yang ◽  
Guirong Sun ◽  
Bingxu Quan ◽  
Jiawei Tang ◽  
Chunhui Zhang ◽  
...  
Keyword(s):  
Sensitivity Analysis ◽  
Removal Efficiency ◽  
Natural Zeolite ◽  
Fluoride Concentration ◽  
Current Work ◽  
Fluoride Removal ◽  
Metal Fluoride ◽  
Modified Zeolite ◽  
X Ray ◽  
Independent Variables

The emerging interest in fluoride-removal from wastewater has attracted attention to zeolite since it has been considered as a natural adsorbent. However, the fluoride-removal efficiency of natural zeolite is generally low. As part of the effort to improve the zeolite adsorption efficiency, we have produced and tested the Mn-Ti modified zeolite. In the current work, the material preparation is discussed, and prepared materials were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy, and Fourier transform infrared (FTIR) spectra. Both static and dynamic experiments were conducted to examine the effects of independent variables. In the static adsorption section, sensitivity analysis experiments were conducted for independent variables, such as adsorbent dosage, pH, temperature, and competitive ions. The maximum adsorption capacity is 2.175 mg/g, which was obtained at PH = 7, temperature = 25 °C, and initial fluoride concentration = 10 mg/L. For adsorption kinetics, both Lagergren and Pseudo-second order models predict the experiments very well, which probably demonstrates that the current process is a combination of physical sorption and chemisorption. For adsorption isotherms, the Freundlich model performs better than the Langmuir model since it is usually applied to illustrate adsorption on inhomogeneous surfaces. In the dynamic adsorption section, sensitivity analysis experiments were also conducted for independent variables, such as adsorbent thickness, flow velocity, initial fluoride concentration, and PH. Additionally, the adsorption mechanism is also discussed. The main reason is the hydrated metal fluoride precipitate formation. As we know, the current work provides the first quantified comparison of the natural zeolite and the Mn-Ti modified zeolite regarding fluoride-removal efficiency.

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