Surface properties of tellurite and fluorotellurite glasses

2007 ◽  
Vol 22 (6) ◽  
pp. 1673-1684 ◽  
Author(s):  
M.D. O’Donnell ◽  
D. Furniss ◽  
V.K. Tikhomirov ◽  
D. Briggs ◽  
E.F. Smith ◽  
...  

The surface properties of some freshly cleaved, or polished, quaternary tellurite glasses (TeO2-ZnO-Na2O-Yb2O3and TeO2-ZnO-Na2O-GeO2) and a proposed ternary fluorotellurite core/clad optical fiber pair (TeO2-N a2O-ZnF2) were investigated by means of x-ray photoelectron spectroscopy and chemical durability. Semiquantitative chemical analysis of the x-ray photoelectron spectroscopy spectra of cleaved tungsten-tellurite and fluorotellurite glasses showed good agreement with the batched at.% values when taking into account the effects of processing (e.g., melt fluorine volatilization), and the samples seemed to exhibit negligible hydrolysis. However, spectra of polished surfaces did not yield useful data because of masking of the glass “signal” from organic contamination at the sample surface. The chemical durability of these glasses were studied; specifically, the glass resistance to the attack and the etchability of various acids (aqueous HF, H2SO4, and HCl), alkali (aqueous NaOH), and water at 15, 21, and 60 °C were obtained by simple mass loss experiments and optical microscopy. Based on the appearance of the glass surfaces after immersion in these solutions, aqueous HF was found to be the most promising etchant, however, infrared spectra showed that significant OH was introduced into the glass. Attack of the fluorotellurite glasses was found to proceed at a higher rate in water at 60 °C compared with room temperature, and at both temperatures was shown to be diffusion controlled, with an Arrhenian activation energy estimated as 57 kJ mol−1.

2014 ◽  
Vol 53 (8S3) ◽  
pp. 08NB05 ◽  
Author(s):  
Jong-Chang Woo ◽  
Chang-Auck Choi ◽  
Woo-Seok Yang ◽  
Yoon-Soo Chun ◽  
Chang-Il Kim

1981 ◽  
Vol 85 (10) ◽  
pp. 1406-1412 ◽  
Author(s):  
P. O. Scokart ◽  
A. Amin ◽  
C. Defosse ◽  
P. G. Rouxhet

Processes ◽  
2019 ◽  
Vol 7 (3) ◽  
pp. 167 ◽  
Author(s):  
Bo Huang ◽  
Guowei Liu ◽  
Penghui Wang ◽  
Xiang Zhao ◽  
Hongxiang Xu

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.


2013 ◽  
Vol 740-742 ◽  
pp. 121-124 ◽  
Author(s):  
Enrique Escobedo-Cousin ◽  
Konstantin Vassilevski ◽  
Toby Hopf ◽  
Nick G. Wright ◽  
Anthony O’Neill ◽  
...  

Few-layers graphene films (FLG) were grown by local solid phase epitaxy on a semi-insulating 6H-SiC substrate by annealing Ni films deposited on the Si and C-terminated faces of the SiC. The impact of the annealing process on the final quality of the FLG films is studied using Raman spectroscopy. X-ray photoelectron spectroscopy was used to verify the presence of graphene on the sample surface. We also demonstrate that further device fabrication steps such as dielectric deposition can be carried out without compromising the FLG films integrity.


2014 ◽  
Vol 26 (2) ◽  
pp. 950-954 ◽  
Author(s):  
Hongquan Yang ◽  
Xiong Zhang ◽  
Shuchang Wang ◽  
Min Zhu ◽  
Yiping Cui ◽  
...  

2014 ◽  
Vol 90 (19) ◽  
Author(s):  
N. Heming ◽  
U. Treske ◽  
M. Knupfer ◽  
B. Büchner ◽  
D. S. Inosov ◽  
...  

2006 ◽  
Vol 20 (25n27) ◽  
pp. 3605-3610 ◽  
Author(s):  
MASAYOSHI MIZUTANI ◽  
JUN KOMOTORI ◽  
KAZUTOSHI KATAHIRA ◽  
HITOSHI OHMORI

The biocompatibility of titanium implants with different surface properties is investigated. We prepared three types of specimens, one ground by the newly developed ELID grinding system, another ground by conventional ELID grinding, and the other polished by SiO 2 powder. These surfaces were characterized and, the number of cell and cytotoxicity in in-vitro were measured. Energy Dispersive X-ray Spectroscopy (EDS), X-ray Photoelectron Spectroscopy (XPS) and Transmission Electron Microscope (TEM) revealed that the modified ELID system can create a significantly thick oxide layer and a diffused oxide layer, and also can control the thickness of a modified layer. The results of cell number and cytotoxicity showed that the sample ground by the modified system had the highest biocompatibility. This may have been caused by improvement of chemical properties due to a surface modified layer. The above results suggest that this newly developed ELID grinding system can create the desirable surface properties. Consequently, this system appears to offer significant future promise for use in biomaterials and other engineering components.


2017 ◽  
Vol 898 ◽  
pp. 2224-2230
Author(s):  
Ying Liang ◽  
Bin Fang ◽  
Fang Fang Lin ◽  
Xu Min Zhu

Ag/rGO composites were synthesized under gamma irradiation using silver nitrate and graphene oxide (GO) as the starting materials. Comparing with traditional methods, gamma irradiation is a simple and “green” technique. In the irradiation system, silver ions were reduced to silver nanoparticles (AgNPs) by the electrons generated from the radiolysis of solvent. GO nanosheets provided reactive sites for the formation of AgNPs and acted as a colloidal surfactant preventing the aggregation of AgNPs. Meanwhile, GO were partially reduced to reduced graphene oxide (rGO). X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscope, transmission electron microscope, Raman spectra and UV-Vis absorption spectra were applied for the characterization of Ag/rGO composites. The results showed that the absorbed dose (3.1 kGy, 4.7 kGy, 9.4 kGy and 27.4 kGy) plays an important role in the size distribution of AgNPs and the reduction degree of GO nanosheetes. The Ag/rGO composites exhibit a broad absorption band at visible light due to the surface plasmon resonance of AgNPs. Because of the unique surface properties, Ag/rGO composites behave enhanced performance for the adsorption of organic dye from water.


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