scholarly journals Effect of Nitric Acid Modification on Characteristics and Adsorption Properties of Lignite

Processes ◽  
2019 ◽  
Vol 7 (3) ◽  
pp. 167 ◽  
Author(s):  
Bo Huang ◽  
Guowei Liu ◽  
Penghui Wang ◽  
Xiang Zhao ◽  
Hongxiang Xu
Keyword(s):  
Nitric Acid ◽  
Surface Chemistry ◽  
Pore Structure ◽  
Surface Properties ◽  
Photoelectron Spectroscopy ◽  
Metal Ion ◽  
Adsorption Properties ◽  
Acid Modification ◽  
X Ray ◽  
Adsorption Performance

The objective of this research was to explore the changes of the pore structure and surface properties of nitric-modified lignite and base the adsorption performance on physical and chemical adsorbent characteristics. To systematically evaluate pore structure and surface chemistry effects, several lignite samples were treated with different concentrations of nitric acid in order to get different pore structure and surface chemistry adsorbent levels. A common heavy metal ion contaminant in water, Pb2+, served as an adsorbate probe to demonstrate the change of modified lignite adsorption properties. The pore structure and surface properties of lignite samples before and after modification were characterized by static nitrogen adsorption, X-ray diffraction, Scanning electron microscope, Fourier transform infrared spectroscopy, zeta potential, and X-ray photoelectron spectroscopy. The experimental results showed that nitric acid modification can increase the ability of lignite to adsorb Pb2+. The adsorption amount of Pb2+ increased from 14.45 mg·g−1 to 30.68 mg·g−1. Nitric acid reacted with inorganic mineral impurities such as iron dolomite in lignite and organic components in coal, which caused an increase in pore size and a decrease in specific surface areas. A hydrophilic adsorbent surface more effectively removed Pb2+ from aqueous solution. Nitric acid treatment increased the content of polar oxygen-containing functional groups such as hydroxyl, carbonyl, and carboxyl groups on the surface of lignite. Treatment introduced nitro groups, which enhanced the negative electrical properties, the polarity of the lignite surface, and its metal ion adsorption performance, a result that can be explained by enhanced water adsorption on hydrophilic surfaces.

scholarly journals Surface Properties of Retrieved Cementless Femoral Hip Endoprostheses Produced from a Ti6Al7Nb Alloy

Coatings ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 868 ◽  
Author(s):  
Klemen Avsec ◽  
Monika Jenko ◽  
Marjetka Conradi ◽  
Aleksandra Kocijan ◽  
Alenka Vesel ◽  
...  
Keyword(s):  
Surface Chemistry ◽  
Aseptic Loosening ◽  
Surface Properties ◽  
Photoelectron Spectroscopy ◽  
Latent Infection ◽  
Electron Back Scatter Diffraction ◽  
Premature Failure ◽  
X Ray ◽  
Angle Measurements ◽  
Physico Chemical

We have investigated new and retrieved cementless hip endoprostheses that prematurely failed due to (i) aseptic loosening, (ii) infection and (iii) latent infection. The aim was to better understand the physico-chemical phenomena on the surfaces and sub-surfaces of the Ti6Al7Nb alloy implant. The results of our studies should enable us to distinguish the causes of premature failure, optimize the surface modification, achieve optimal osseointegration and extend the useful lifetime of the implants. The surface properties of the Ti6Al7Nb alloys of the hip-stem endoprostheses (30 retrieved and 2 new) were determined by contact-angle measurements and the average surface roughness. The surface chemistry and microstructure were analysed by scanning electron microscopy (SEM) for morphology, energy-dispersive X-ray spectroscopy (EDS) for the chemistry, and electron back-scatter diffraction (EBSD) for the phase analysis; Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS) for the surface chemistry; and electrochemical measurements for the corrosion. The improved wettability of the grit-blasted surface of the Ti6Al7Nb stems after autoclaving was measured, as was the super wettability after oxygen-plasma sterilization. The secondary-electron images showed that the morphology and microstructure of the new and retrieved stems (prematurely failed due to aseptic loosening, infection and latent infection) differ slightly, while the EDS analysis revealed corundum contamination of the grit-blasted surface. We found corundum-contaminated Ti6Al7Nb stem surfaces and sub-surfaces for all the investigated new and retrieved implants. These residues are a potential problem, i.e., third-body wear particles, and probably induce the osteolysis and aseptic loosening.

Surface properties of ZrO2thin film under Cl2/Ar plasma using angle-resolved X-ray photoelectron spectroscopy

2014 ◽  
Vol 53 (8S3) ◽  
pp. 08NB05 ◽  
Author(s):  
Jong-Chang Woo ◽  
Chang-Auck Choi ◽  
Woo-Seok Yang ◽  
Yoon-Soo Chun ◽  
Chang-Il Kim
Keyword(s):  
Surface Properties ◽  
Photoelectron Spectroscopy ◽  
X Ray ◽  
Ar Plasma

Direct probing of the surface properties of alkali-treated aluminas by infrared and x-ray photoelectron spectroscopy

1981 ◽  
Vol 85 (10) ◽  
pp. 1406-1412 ◽  
Author(s):  
P. O. Scokart ◽  
A. Amin ◽  
C. Defosse ◽  
P. G. Rouxhet
Keyword(s):  
Surface Properties ◽  
Photoelectron Spectroscopy ◽  
X Ray

Structural and Catalytic Properties of the Alkali Metal Ion-Exchanged Y-Zeolites by 29Si and 27Al Solid-State NMR and FT-IR Spectroscopy

2005 ◽  
Vol 277-279 ◽  
pp. 708-719
Author(s):  
Chang Seop Lee ◽  
Hee Jung Lee ◽  
Sung Woo Choi ◽  
Jahun Kwak ◽  
Charles H.F. Peden
Keyword(s):  
Solid State ◽  
Alkali Metal ◽  
Photoelectron Spectroscopy ◽  
Metal Ion ◽  
Nmr Spectra ◽  
Catalytic Properties ◽  
Nox Reduction ◽  
29Si Nmr ◽  
Y Zeolites ◽  
X Ray

A series of cation exchanged Y-zeolites were prepared by exchanging cations with various alkali (M+, M= Li, Na, K, Cs) metals. The structural and catalytic properties of the alkali metal exchanged Y-zeolites have been investigated by a number of analytical techniques. Comparative elemental analyses were determined by an Energy Dispersive Spectroscopy X-ray (EDS), X-ray Photoelectron Spectroscopy (XPS), Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) and X-ray Fluorescence (XRF) before and after cation substitution. The framework and non-framework Al coordination and the Si/Al ratios of the Y-zeolites were investigated by MAS Solid-State Nuclear Magnetic Resonance (NMR) spectroscopy. The Al NMR spectra were characterized by two 27Al resonance signals at 12 and 59 ppm, indicating the presence of the non-framework and framework Al respectively. The intensities of these resonances were used to monitor the amount of the framework and non-framework Al species in the series of exchanged zeolites. The 29Si NMR spectra were characterized by four resonance signals at -79, -84, -90, and -95 ppm. Changing the alkali metal cations in the exchanged Y-zeolites significantly altered the extent of the octahedral/tetrahedral coordination and the Si/Al ratio. The Fourier Transform Infrared spectra of the CO2 adsorbed on to the exchanged Y-zeolites showed a low frequency shift, as the atomic number of the exchanged alkali metal increased. In addition, the catalytic activity of these samples for NOx reduction were tested in combination with a non-thermal plasma technique and interpreted based on the above structural and spectroscopic information.

Removal of Pb(II) and Cu(II) from aqueous solution using multiwalled carbon nanotubes/iron oxide magnetic composites

2011 ◽  
Vol 63 (5) ◽  
pp. 917-923 ◽  
Author(s):  
Jun Hu ◽  
Donglin Zhao ◽  
Xiangke Wang
Keyword(s):  
Carbon Nanotubes ◽  
Iron Oxide ◽  
Multiwalled Carbon Nanotubes ◽  
Sorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Metal Ion ◽  
Precipitation Method ◽  
Multiwalled Carbon ◽  
Magnetic Composites ◽  
X Ray

Multiwalled carbon nanotubes (MWCNTs)/iron oxide magnetic composites (named as MCs) were prepared by co-precipitation method, and were characterised by scanning electron microscope (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) in detail. The prepared MCs were employed as an adsorbent for the removal of Pb(II) and Cu(II) ions from wastewater in heavy metal ion pollution cleanup. The results demonstrated that the sorption of Pb(II) and Cu(II) ions was strongly dependent on pH and temperature. The experimental data were well described by Langmuir model, and the monolayer sorption capacity of MCs was found to vary from 10.02 to 31.25 mg/g for Pb(II) and from 3.11 to 8.92 mg/g for Cu(II) at temperature increasing from 293.15 to 353.15 K at pH 5.50. The sorption capacity of Pb(II) on MCs was higher than that of Cu(II), which was attributed to their ionic radius, hydration energies and hydrolysis of their hydroxides. The thermodynamic parameters (i.e., ΔH0, ΔS0 and ΔG0) were calculated from temperature dependent sorption isotherms, and the results indicated that the sorption of Pb(II) and Cu(II) ions on MCs were spontaneous and endothermic processes.

scholarly journals Surface Chemistry of Carbon Dioxide on Copper Model Catalysts Studied by Ambient-Pressure X-ray Photoelectron Spectroscopy

2019 ◽  
Vol 17 (0) ◽  
pp. 169-178 ◽  
Author(s):  
Takanori Koitaya ◽  
Susumu Yamamoto ◽  
Iwao Matsuda ◽  
Jun Yoshinobu
Keyword(s):  
Carbon Dioxide ◽  
Surface Chemistry ◽  
Photoelectron Spectroscopy ◽  
Ambient Pressure ◽  
Model Catalysts ◽  
X Ray

Surface Analysis, Microstructural Characterization and Local Corrosion Processes in Decarburized SAE 9254 Spring Steel

CORROSION ◽  
10.5006/3234 ◽  
2019 ◽  
Vol 75 (12) ◽  
pp. 1474-1486
Author(s):  
Jéssica Cristina Costa de Castro Santana ◽  
Rejane Maria Pereira da Silva ◽  
Renato Altobelli Antunes ◽  
Sydney Ferreira Santos
Keyword(s):  
Surface Chemistry ◽  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Microstructural Characterization ◽  
Spring Steel ◽  
Laser Scanning Microscopy ◽  
Local Corrosion ◽  
Confocal Laser ◽  
X Ray ◽  
Decarburized Layer

The aim of the present work was to study the surface chemistry, microstructure, and local corrosion processes at the decarburized layer of the SAE 9254 automotive spring steel. The samples were austenitized at 850°C and 900°C, and oil quenched. The microstructure was investigated using confocal laser scanning microscopy and scanning electron microscopy. The surface chemistry was analyzed by x-ray photoelectron spectroscopy. Electrochemical impedance spectroscopy and potentiodynamic polarization were used to assess the global corrosion behavior of the decarburized samples. Scanning electrochemical microscopy was used to evaluate the influence of decarburization on the local corrosion activity. Microstructural characterization and x-ray photoelectron spectroscopy analysis indicate a dependence of the local electrochemical processes with the steel microconstituents and Si oxides in the decarburized layer.

Surface chemistry studied by in situ X-ray photoelectron spectroscopy

2005 ◽  
Vol 80 (5) ◽  
pp. 977-986 ◽  
Author(s):  
R. Denecke
Keyword(s):  
Surface Chemistry ◽  
Photoelectron Spectroscopy ◽  
X Ray
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