scholarly journals Design of Scorodite@Fe3O4 Core–Shell Materials and the Fe3O4 Shell Prevents Leaching of Arsenic from Scorodite in Neutral and Alkaline Environments

Coatings ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 523
Author(s):  
Yang Wang ◽  
Zhihao Rong ◽  
Xincun Tang ◽  
Shan Cao
Keyword(s):  
Photoelectron Spectroscopy ◽  
Shell Structure ◽  
Molar Ratio ◽  
Alkaline Solutions ◽  
Arsenic Content ◽  
Core Shell ◽  
X Ray ◽  
Core Shell Structure ◽  
The Stability ◽  
Fe3o4 Core

In recent years, arsenic pollution has seriously harmed human health. Arsenic-containing waste should be treated to render it harmless and immobilized to form a stable, solid material. Scorodite (iron arsenate) is recognized as the best solid arsenic material in the world. It has the advantages of high arsenic content, good stability, and a low iron/arsenic molar ratio. However, scorodite can decompose and release arsenic in a neutral and alkaline environment. Ferroferric oxide (Fe3O4) is a common iron oxide that is insoluble in acid and alkali solutions. Coating a Fe3O4 shell that is acid- and alkali-resistant on the surface of scorodite crystals will improve the stability of the material. In this study, a scorodite@Fe3O4 core–shell structure material was synthesized. The synthesized core–shell material was detected by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Raman, and energy-dispersive X-ray spectroscopy (EDS) techniques, and the composition and structure were confirmed. The synthesis condition and forming process were analyzed. Long-term leaching tests were conducted to evaluate the stability of the synthesized scorodite@Fe3O4. The results indicate that the scorodite@Fe3O4 had excellent stability after 20 days of exposure to neutral and weakly alkaline solutions. The inert Fe3O4 shell could prevent the scorodite core from corrosion by the external solution. The scorodite@Fe3O4 core–shell structure material was suitable for the immobilization of arsenic and has potential application prospects for the treatment of arsenic-containing waste.

Direct Verification of the Core−Shell Structure of Shell Cross-Linked Micelles in the Solid State Using X-ray Photoelectron Spectroscopy

Langmuir ◽  
2002 ◽  
Vol 18 (21) ◽  
pp. 7780-7784 ◽  
Author(s):  
Shiyong Liu ◽  
Yinghua Ma ◽  
Steven P. Armes ◽  
C. Perruchot ◽  
J. F. Watts
Keyword(s):  
Solid State ◽  
Photoelectron Spectroscopy ◽  
Shell Structure ◽  
Core Shell ◽  
X Ray ◽  
Direct Verification ◽  
The Core ◽  
Core Shell Structure

Prepared and Microwave-Absorption Properties of SiC Coated Ni Nanocapsules

2011 ◽  
Vol 217-218 ◽  
pp. 152-157 ◽  
Author(s):  
Gui Mei Shi ◽  
Jin Bing Zhang ◽  
Shu Lian ◽  
Long Shan Chen
Keyword(s):  
Reflection Loss ◽  
Photoelectron Spectroscopy ◽  
Shell Structure ◽  
Core Shell ◽  
Absorber Thickness ◽  
Frequency Range ◽  
Absorption Properties ◽  
Microwave Absorption Properties ◽  
X Ray ◽  
Core Shell Structure

SiC coated Ni nanocapsules were prepared by arc evaporating the mixture of Ni and SiC powders in Ar and H2 atmosphere. HRTEM shows the as-prepared nanoparticles form in a core¬¬¬-shell structure, with the size of nanoparticles in range of 20-50nm and the thickness of the shell 2-6nm. X-Ray and X-ray photoelectron spectroscopy show core consist of Ni, while the shell consists of SiC. The core-shell structure can prevent Ni nanoparticles from oxidation and agglomeration. The electromagnetic characters were measured by Agilent 8722ES microwave network analyzer in the band of 2-18GHz. The reflection loss R(dB) of less than –20 dB was obtained in the frequency range of 3.8-11.1GHz with absorber thickness of 2.5–5mm, An optimal reflection loss of –33.4dB was reached at 7.4GHz with an absorber thickness of 3.5mm.In addition, the optimal RL obviously shifts to the lower-frequency range with increasing thickness of the layer.

Core–shell stability of nanoparticles plays an important role for overcoming the intestinal mucus and epithelium barrier

2016 ◽  
Vol 4 (35) ◽  
pp. 5831-5841 ◽  
Author(s):  
Min Liu ◽  
Lei Wu ◽  
Xi Zhu ◽  
Wei Shan ◽  
Lian Li ◽  
...  
Keyword(s):  
Shell Structure ◽  
Core Shell ◽  
The Core ◽  
Shell Stability ◽  
Intestinal Mucus ◽  
Core Shell Structure ◽  
The Stability

The stability of the core–shell structure plays an important role in the nanoparticles ability to overcome both the mucus and epithelium absorption barrier.

scholarly journals Well-Dispersed Nanoscale Zero-Valent Iron Supported in Macroporous Silica Foams: Synthesis, Characterization, and Performance in Cr(VI) Removal

2017 ◽  
Vol 2017 ◽  
pp. 1-13 ◽  
Author(s):  
Chaoxia Zhao ◽  
Jie Yang ◽  
Yihan Wang ◽  
Bo Jiang
Keyword(s):  
Removal Efficiency ◽  
Shell Structure ◽  
Zero Valent Iron ◽  
Core Shell ◽  
Ambient Atmosphere ◽  
Order Kinetic ◽  
Macroporous Silica ◽  
X Ray ◽  
Nanoscale Zero Valent Iron ◽  
Core Shell Structure

Well-dispersed nanoscale zero-valent iron (NZVI) supported inside the pores of macroporous silica foams (MOSF) composites (Mx-NZVI) has been prepared as the Cr(VI) adsorbent by simply impregnating the MOSF matrix with ferric chloride, followed by the chemical reduction with NaHB4 in aqueous solution at ambient atmosphere. Through the support of MOSF, the reactivity and stability of NZVI are greatly improved. Transmission electron microscopy (TEM) results show that NZVI particles are spatially well-dispersed with a typical core-shell structure and supported inside MOSF matrix. The N2 adsorption-desorption isotherms demonstrate that the Mx-NZVI composites can maintain the macroporous structure of MOSF and exhibit a considerable high surface area (503 m2·g−1). X-ray photoelectron spectroscopy (XPS) and powder X-ray diffraction (XRD) measurements confirm the core-shell structure of iron nanoparticles composed of a metallic Fe0 core and an Fe(II)/Fe(III) species shell. Batch experiments reveal that the removal efficiency of Cr(VI) can reach 100% when the solution contains 15.0 mg·L−1 of Cr(VI) at room temperature. In addition, the solution pH and the composites dosage can affect the removal efficiency of Cr(VI). The Langmuir isotherm is applicable to describe the removal process. The kinetic studies demonstrate that the removal of Cr(VI) is consistent with pseudo-second-order kinetic model.

scholarly journals Lead-Free BNT–BT0.08/CoFe2O4 Core–Shell Nanostructures with Potential Multifunctional Applications

Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 672
Author(s):  
Marin Cernea ◽  
Roxana Radu ◽  
Harvey Amorín ◽  
Simona Gabriela Greculeasa ◽  
Bogdan Stefan Vasile ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Molar Ratio ◽  
Transmission Electron Microscopy Data ◽  
Core Shell ◽  
Shell Nanoparticles ◽  
Two Phase ◽  
X Ray ◽  
Shell Nanostructures

Herein we report on novel multiferroic core–shell nanostructures of cobalt ferrite (CoFe2O4)–bismuth, sodium titanate doped with barium titanate (BNT–BT0.08), prepared by a two–step wet chemical procedure, using the sol–gel technique. The fraction of CoFe2O4 was varied from 1:0.5 to 1:1.5 = BNT–BT0.08/CoFe2O4 (molar ratio). X–ray diffraction confirmed the presence of both the spinel CoFe2O4 and the perovskite Bi0.5Na0.5TiO3 phases. Scanning electron microscopy analysis indicated that the diameter of the core–shell nanoparticles was between 15 and 40 nm. Transmission electron microscopy data showed two–phase composite nanostructures consisting of a BNT–BT0.08 core surrounded by a CoFe2O4 shell with an average thickness of 4–7 nm. Cole-Cole plots reveal the presence of grains and grain boundary effects in the BNT–BT0.08/CoFe2O4 composite. Moreover, the values of the dc conductivity were found to increase with the amount of CoFe2O4 semiconductive phase. Both X-ray photoelectron spectroscopy (XPS) and Mössbauer measurements have shown no change in the valence of the Fe3+, Co2+, Bi3+ and Ti4+ cations. This study provides a detailed insight into the magnetoelectric coupling of the multiferroic BNT–BT0.08/CoFe2O4 core–shell composite potentially suitable for magnetoelectric applications.

Preparation of Amorphous Calcium Phosphate/Triclcium Silicate Composite Powders

2009 ◽  
Vol 79-82 ◽  
pp. 1643-1646 ◽  
Author(s):  
Qing Lin ◽  
Yan Bao Li ◽  
Xiang Hui Lan ◽  
Chun Hua Lu ◽  
Zhong Zi Xu
Keyword(s):  
Calcium Phosphate ◽  
Shell Structure ◽  
Amorphous Calcium Phosphate ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
X Ray ◽  
Core Shell Structure

The amorphous calcium phosphate (ACP)/tricalcium silicate (Ca3SiO5, C3S) composite powders were synthesized in this paper. The exothermal behavior of C3S determined by isothermal conduction calorimetry indicated that the ACP could be synthesis by chemical precipitation method during the induction period (stage II) of C3S. The composite powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The results indicated that nanosized ACP particles deposited on the surface of C3S particles to form core-shell structure at pH=10.5, and the nCa/nP of ACP could be controlled between 1.0 and 1.5. The core-shell structure is stable after sintered at 500 oC for 3 h to remove the β-cyclodextrin (β-CD). As compared with the irregular C3S particles (1~5 μm), the composite powders particles are spherical with a diameter of 40~150 μm. Therefore, to obtain the smaller size of composite powders, it is expected to avoid the aggregate of C3S particles in the aqueous solution by addition of dispersant. As compared with C3S, the composite powders may contribute better injectability, strength and biocompatibility.

scholarly journals Core/Shell Structure of TiO2-Coated MWCNTs for Thermal Protection for High-Temperature Processing of Metal Matrix Composites

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Laura Angélica Ardila Rodriguez ◽  
Dilermando Nagle Travessa
Keyword(s):  
Thermal Stability ◽  
Metal Matrix Composites ◽  
Shell Structure ◽  
Metal Matrix ◽  
Thermal Protection ◽  
Oxidation Stability ◽  
Core Shell ◽  
Matrix Composites ◽  
X Ray ◽  
Core Shell Structure

The production of metal matrix composites with elevated mechanical properties depends largely on the reinforcing phase properties. Due to the poor oxidation resistance of multiwalled carbon nanotubes (MWCNTs) as well as their high reactivity with molten metal, the processing conditions for the production of MWCNT-reinforced metal matrix composites may be an obstacle to their successful use as reinforcement. Coating MWCNTs with a ceramic material that acts as a thermal protection would be an alternative to improve oxidation stability. In this work, MWCNTs previously functionalized were coated with titanium dioxide (TiO2) layers of different thicknesses, producing a core-shell structure. Heat treatments at three different temperatures (500°C, 750°C, and 1000°C) were performed on coated nanotubes in order to form a stable metal oxide structure. The MWCNT/TiO2 hybrids produced were evaluated in terms of thermal stability. Thermogravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy (RS), and X-ray photoelectron spectroscopy (XPS) were performed in order to investigate TiO2-coated MWCNT structure and thermal stability under oxidative atmosphere. It was found that the thermal stability of the TiO2-coated MWCNTs was dependent of the TiO2 layer morphology that in turn depends on the heat treatment temperature.

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