scholarly journals Synthesis of Zeolite 4A from Kaolin and Its Adsorption Equilibrium of Carbon Dioxide

Materials ◽  
2019 ◽  
Vol 12 (9) ◽  
pp. 1536 ◽  
Author(s):  
Peng Wang ◽  
Qi Sun ◽  
Yujiao Zhang ◽  
Jun Cao
Keyword(s):  
Electron Microscopy ◽  
Carbon Dioxide ◽  
Adsorption Equilibrium ◽  
Magic Angle ◽  
Low Grade ◽  
Carbon Dioxide Adsorption ◽  
X Ray ◽  
Adsorption Analysis ◽  
Bet Analysis ◽  
Zeolite 4A

Zeolite 4A was successfully prepared by hydrothermal synthesis using low-grade kaolin as a raw material. The properties of the synthesized zeolite 4A were characterized by means of X-ray diffraction (XRD), Fourier transform infrared (FTIR), 29Si magic-angle spinning (MAS)-nuclear magnetic resonance (NMR) and 27Al MAS-NMR, X-ray fluorescence (XRF), scanning electron microscopy (SEM)-energy-dispersive spectrometry (EDS), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET), thermogravimetry (TG)-differential thermal analysis (DTA), and carbon dioxide adsorption analysis. The textural properties of the synthesized zeolite 4A was further studied by BET analysis technique. The thermal stability analysis showed that the heat resistance of the synthesized zeolite 4A is up to 940 °C. In addition, it is found that the Langmuir model has the best agreement with the adsorption equilibrium data for carbon dioxide by synthesized zeolite 4A and commercial zeolite 4A. Meanwhile, the carbon dioxide adsorption analysis confirmed that the maximum equilibrium adsorption amount of carbon dioxide on synthesized zeolite 4A is 59.3820 mL/g, which is higher than the 55.4303 mL/g of the commercial zeolite 4A.

scholarly journals Solid-State Ball-Milling of Co3O4 Nano/Microspheres and Carbon Black Endorsed LaMnO3 Perovskite Catalyst for Bifunctional Oxygen Electrocatalysis

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 76
Author(s):  
Chelladurai Karuppiah ◽  
Balamurugan Thirumalraj ◽  
Srinivasan Alagar ◽  
Shakkthivel Piraman ◽  
Ying-Jeng Jame Li ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Energy Storage ◽  
Fuel Cell ◽  
Solid State ◽  
Carbon Black ◽  
Ball Milling ◽  
Potential Candidate ◽  
X Ray ◽  
Bifunctional Electrocatalyst ◽  
Bet Analysis

Developing a highly stable and non-precious, low-cost, bifunctional electrocatalyst is essential for energy storage and energy conversion devices due to the increasing demand from the consumers. Therefore, the fabrication of a bifunctional electrocatalyst is an emerging focus for the promotion and dissemination of energy storage/conversion devices. Spinel and perovskite transition metal oxides have been widely explored as efficient bifunctional electrocatalysts to replace the noble metals in fuel cell and metal-air batteries. In this work, we developed a bifunctional catalyst for oxygen reduction and oxygen evolution reaction (ORR/OER) study using the mechanochemical route coupling of cobalt oxide nano/microspheres and carbon black particles incorporated lanthanum manganite perovskite (LaMnO3@C-Co3O4) composite. It was synthesized through a simple and less-time consuming solid-state ball-milling method. The synthesized LaMnO3@C-Co3O4 composite was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, Brunauer-Emmett-Teller (BET) analysis, X-ray diffraction spectroscopy, and micro-Raman spectroscopy techniques. The electrocatalysis results showed excellent electrochemical activity towards ORR/OER kinetics using LaMnO3@C-Co3O4 catalyst, as compared with Pt/C, bare LaMnO3@C, and LaMnO3@C-RuO2 catalysts. The observed results suggested that the newly developed LaMnO3@C-Co3O4 electrocatalyst can be used as a potential candidate for air-cathodes in fuel cell and metal-air batteries.

scholarly journals Assessment of SnFe2O4 Nanoparticles for Potential Application in Theranostics: Synthesis, Characterization, In Vitro, and In Vivo Toxicity

Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 825
Author(s):  
Saman Sargazi ◽  
Mohammad Reza Hajinezhad ◽  
Abbas Rahdar ◽  
Muhammad Nadeem Zafar ◽  
Aneesa Awan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
A549 Cells ◽  
In Vitro Cytotoxicity ◽  
Hek293 Cells ◽  
Hydrothermal Route ◽  
X Ray ◽  
Tin Chloride ◽  
Bet Analysis

In this research, tin ferrite (SnFe2O4) NPs were synthesized via hydrothermal route using ferric chloride and tin chloride as precursors and were then characterized in terms of morphology and structure using Fourier-transform infrared spectroscopy (FTIR), Ultraviolet–visible spectroscopy (UV-Vis), X-ray power diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), and Brunauer–Emmett–Teller (BET) method. The obtained UV-Vis spectra was used to measure band gap energy of as-prepared SnFe2O4 NPs. XRD confirmed the spinel structure of NPs, while SEM and TEM analyses disclosed the size of NPs in the range of 15–50 nm and revealed the spherical shape of NPs. Moreover, energy dispersive X-ray spectroscopy (EDS) and BET analysis was carried out to estimate elemental composition and specific surface area, respectively. In vitro cytotoxicity of the synthesized NPs were studied on normal (HUVEC, HEK293) and cancerous (A549) human cell lines. HUVEC cells were resistant to SnFe2O4 NPs; while a significant decrease in the viability of HEK293 cells was observed when treated with higher concentrations of SnFe2O4 NPs. Furthermore, SnFe2O4 NPs induced dramatic cytotoxicity against A549 cells. For in vivo study, rats received SnFe2O4 NPs at dosages of 0, 0.1, 1, and 10 mg/kg. The 10 mg/kg dose increased serum blood urea nitrogen and creatinine compared to the controls (P < 0.05). The pathology showed necrosis in the liver, heart, and lungs, and the greatest damages were related to the kidneys. Overall, the in vivo and in vitro experiments showed that SnFe2O4 NPs at high doses had toxic effects on lung, liver and kidney cells without inducing toxicity to HUVECs. Further studies are warranted to fully elucidate the side effects of SnFe2O4 NPs for their application in theranostics.

scholarly journals A Highly Sensitive Room Temperature CO2 Gas Sensor Based on SnO2-rGO Hybrid Composite

Materials ◽  
2021 ◽  
Vol 14 (3) ◽  
pp. 522
Author(s):  
Zhi Yan Lee ◽  
Huzein Fahmi bin Hawari ◽  
Gunawan Witjaksono bin Djaswadi ◽  
Kamarulzaman Kamarudin
Keyword(s):  
Electron Microscopy ◽  
Carbon Dioxide ◽  
Gas Sensor ◽  
Photoelectron Spectroscopy ◽  
Hybrid Composite ◽  
Room Temperature ◽  
Co2 Gas ◽  
X Ray ◽  
Wide Range ◽  
Co2 Gas Sensor

A tin oxide (SnO2) and reduced graphene oxide (rGO) hybrid composite gas sensor for high-performance carbon dioxide (CO2) gas detection at room temperature was studied. Since it can be used independently from a heater, it emerges as a promising candidate for reducing the complexity of device circuitry, packaging size, and fabrication cost; furthermore, it favors integration into portable devices with a low energy density battery. In this study, SnO2-rGO was prepared via an in-situ chemical reduction route. Dedicated material characterization techniques including field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), energy dispersive X-ray (EDX) spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS) were conducted. The gas sensor based on the synthesized hybrid composite was successfully tested over a wide range of carbon dioxide concentrations where it exhibited excellent response magnitudes, good linearity, and low detection limit. The synergistic effect can explain the obtained hybrid gas sensor’s prominent sensing properties between SnO2 and rGO that provide excellent charge transport capability and an abundance of sensing sites.

Relative Reactivity Trends OP High Temperature Superconductor Phases

1992 ◽  
Vol 275 ◽  
Author(s):  
David R. Riley ◽  
Ji-Ping Zhou ◽  
A. Manthiram ◽  
John T. McDevitt
Keyword(s):  
Electron Microscopy ◽  
Carbon Dioxide ◽  
High Temperature ◽  
High Temperature Superconductor ◽  
Relative Reactivity ◽  
Complete Understanding ◽  
High Tc ◽  
X Ray ◽  
The Common ◽  
Scanning Electron

ABSTRACTMany of the high temperature superconductor phases degrade rapidly when in the presence of water, acids, carbon dioxide or carbon monoxide. In order to foster more rapid developments in the area of high-Tc research, it will be necessary to acquire a more complete understanding of the surface chemistry of these superconducting materials. In this paper, the relative reactivity of the common cuprate phases toward water is reported. X-ray powder diffraction and scanning electron microscopy measurements are utilized here to establish the reactivity trends.

Sonochemistry: a good, fast and clean method to promote the removal of Cu(ii) and Cr(vi) by MWCNT/CoFe2O4@PEI nanocomposites: optimization study

2018 ◽  
Vol 42 (19) ◽  
pp. 16307-16328 ◽  
Author(s):  
Mohammad Hassan Omidi ◽  
Mohammad Hossein Ahmadi Azqhandi ◽  
Bahram Ghalami-Choobar
Keyword(s):  
Electron Microscopy ◽  
X Ray Diffraction ◽  
Multiwalled Carbon ◽  
X Ray ◽  
Transmission Electron ◽  
Optimization Study ◽  
Bet Analysis ◽  
Branched Polyethylenimine ◽  
Magnetic Multiwalled Carbon Nanotubes ◽  
Scanning Electron

In this study, branched polyethylenimine (PEI) loaded on magnetic multiwalled carbon nanotubes (MWCNT/CoFe2O4) was synthesized and characterized by transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) analysis and Fourier transform infrared spectroscopy (FTIR).

Carbon dioxide adsorption and activation on gallium phosphide surface monitored by ambient pressure x-ray photoelectron spectroscopy

2021 ◽  
Vol 54 (23) ◽  
pp. 234002
Author(s):  
Yifan Ye ◽  
Hongyang Su ◽  
Kyung-Jae Lee ◽  
David Larson ◽  
Carlos Valero-Vidal ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Photoelectron Spectroscopy ◽  
Gallium Phosphide ◽  
Ambient Pressure ◽  
Carbon Dioxide Adsorption ◽  
X Ray

Mixed-layer mica-chlorite in very low-grade metaclastites from the Malàguide Complex (Betic Cordilleras, Spain)

Clay Minerals ◽  
2001 ◽  
Vol 36 (3) ◽  
pp. 307-324 ◽  
Author(s):  
M. D. Ruiz Cruz
Keyword(s):  
Electron Microscopy ◽  
Mixed Layer ◽  
Analytical Electron Microscopy ◽  
Low Grade ◽  
X Ray ◽  
Betic Cordilleras ◽  
Transmission Electron ◽  
Analytical Electron ◽  
Microscopy Data ◽  
Ray Patterns

AbstractMixed-layered phyllosilicates with composition intermediate between mica and chlorite were identified in very low-grade metaclastites from the Malàguide Complex (Betic Cordilleras, Spain), and studied by X-ray diffraction, and transmission and analytical electron microscopy. They occur both as small grains in the rock matrix, and associated with muscovitechlorite stacks. Transmission electron microscope observations revealed a transition from chlorite to ordered 1:1 interstratifications through complex 1:2 and 1:3 interstratifications. Analytical electron microscopy data indicate a composition slightly different from the sum of discrete trioctahedral chlorite and dioctahedral mica. The types of layer transitions suggest that mixed-layer formation included two main processes: (1) the replacement of a brucite sheet by a cation sheet in the chlorite structure; and (2) the precipitation of mica-like layers between the chlorite layers. The strongest diffraction lines in oriented X-ray patterns are: 12.60 Å (002), 7.98 Å (003), 4.82 Å (005) and 3.48 Å (007).

scholarly journals Analysis of Coal Swelling Deformation Caused by Carbon Dioxide Adsorption Based on X-Ray Computed Tomography

Geofluids ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Xiangrong Nie ◽  
Junbin Chen ◽  
Yi Cao ◽  
Diguang Gong ◽  
Hao Deng
Keyword(s):  
Computed Tomography ◽  
Carbon Dioxide ◽  
Ct Scanning ◽  
Geologic Sequestration ◽  
Carbon Dioxide Adsorption ◽  
X Ray ◽  
Coal Beds ◽  
Coal Swelling ◽  
X Ray Computed ◽  
As Adsorption

The geologic sequestration of carbon dioxide by coal beds leads to the swelling deformation of coal. In order to investigate the swelling deformation characteristics at the microscopic scale, X-ray computed tomography (CT) scanning technology was used. X-ray CT scanning technology detects the internal structure, deformation, and porosity of coal at different gas pressures. Results show that swelling deformation is nonuniform, which is caused by the heterogeneity of the coal structure. Through quantitative measurement of the distance between fractures and pseudocolor processing of CT images, we observed that fractures gradually close with the increase of adsorption pressure. As adsorption pressure increases, the porosity of coal decreases, and the density of coal increases.

scholarly journals Extraction of Phosphorous from a Phosphorous-Containing Vanadium Titano-Magnetite Tailings by Direct Flotation

Processes ◽  
2020 ◽  
Vol 8 (7) ◽  
pp. 874 ◽  
Author(s):  
Junhui Xiao ◽  
Chao Chen ◽  
Wei Ding ◽  
Yang Peng ◽  
Tao Chen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Paraffin Wax ◽  
Low Grade ◽  
X Ray Diffraction ◽  
Flotation Process ◽  
X Ray ◽  
Pine Oil ◽  
Flotation Concentration ◽  
Scanning Electron

In this study, there is 1.42% P2O5 in the P-containing V-Ti magnetite tailings in Miyi Region of China, with the valuable minerals mainly including apatite, and aluminosilicate minerals as the main gangue components. The direction flotation process was used to recover phosphorous from the low-grade phosphorous-bearing V-Ti magnetite tailings. The results showed that an optimized phosphorous concentrate with a P2O5 grade of 31.35% and P2O5 recovery of 88.02% was obtained by flotation process of one roughing, three scavengings, and three cleanings under roughing conditions, which employed pulp pH of 9, grinding fineness of <0.039 mm occupying 90%, flotation concentration of 25%, and dosages of carboxymethylcellulose, oxidized paraffin wax soap, and pine oil of 400 g/t, 300 g/t, and 20 g/t, respectively. Optimized one scavenging, two scavenging, and three scavenging conditions used a pulp pH of 9, and dosages of carboxymethylcellulose, oxidized paraffin wax soap, and pine oil of 200 g/t, 150 g/t, 10 g/t; 100 g/t, 75 g/t, and 5 g/t; and 100 g/t, 75 g/t, and 5 g/t, respectively. Optimized one cleaning, two cleaning, and three cleaning condition dosages of carboxymethylcellulose of 100 g/t, 50 g/t, and 25 g/t, respectively. Study of analysis and characterization of phosphorous concentrate by X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) show that most gangue minerals enter the flotation tailings, the main minerals in phosphorous concentrate are apatite, olivine, and feldspar.

scholarly journals Preparation of TiO2 and Fe-TiO2 with an Impinging Stream-Rotating Packed Bed by the Precipitation Method for the Photodegradation of Gaseous Toluene

Nanomaterials ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 1173 ◽  
Author(s):  
Guangping Zeng ◽  
Qiaoling Zhang ◽  
Youzhi Liu ◽  
Shaochuang Zhang ◽  
Jing Guo
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Packed Bed ◽  
Pure Tio2 ◽  
Precipitation Method ◽  
Nano Tio2 ◽  
X Ray ◽  
Rotating Packed Bed ◽  
Bet Analysis ◽  
Gaseous Toluene

Nano-TiO2 has always been one of the most important topics in the research of photocatalysts due to its special activity and stability. However, it has always been difficult to obtain nano-TiO2 with high dispersion, a small particle size and high photocatalytic activity. In this paper, nano-TiO2 powder was prepared by combining the high-gravity technique and direct precipitation method in an impinging stream-rotating packed bed (IS-RPB) reactor followed by Fe3+ in-situ doping. TiOSO4 and NH3·H2O solutions were cut into very small liquid microelements by high-speed rotating packing, and the mass transfer and microscopic mixing of the nucleation and growth processes of nano-TiO2 were strengthened in IS-RPB, which was beneficial to the continuous production of high quality nano-TiO2. Pure TiO2 and iron-doped nano-TiO2 (Fe-TiO2) were obtained in IS-RPB and were investigated by means of X-ray diffraction (XRD), Raman, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS) and Brunauer–Emmett–Teller (BET) analysis, which found that pure TiO2 had a particle size of about 12.5 nm, good dispersibility and a complete anatase crystal at the rotating speed of packing of 800 rpm and calcination temperature of 500 °C. The addition of Fe3+ did not change the crystalline structure of TiO2. Iron was highly dispersed in TiO2 without the detection of aggregates and was found to exist in a positive trivalent form by XPS. With the increase of iron doping, the photoresponse range of TiO2 to visible light was broadened from 3.06 eV to 2.26 eV. The degradation efficiency of gaseous toluene by Fe-TiO2 under ultraviolet light was higher than that of pure TiO2 and commercial P25 due to Fe3+ effectively suppressing the recombination of TiO2 electrons and holes; the highest efficiency produced by 1.0% Fe-TiO2 was 95.7%.

Sign in / Sign up

Export Citation Format

Share Document