scholarly journals Mechanical and Structural Properties of Nanocomposite CrAlSiN–AlSiN Coating with Periodically Modulated Composition

Coatings ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 41 ◽  
Author(s):  
Lilyana Kolaklieva ◽  
Roumen Kakanakov ◽  
Plamen Stefanov ◽  
Daniela Kovacheva ◽  
Genoveva Atanasova ◽  
...  
Keyword(s):  
Elastic Modulus ◽  
Photoelectron Spectroscopy ◽  
Elastic Recovery ◽  
Effective Elastic Modulus ◽  
X Ray Diffraction ◽  
X Ray ◽  
Composition And Structure ◽  
Cathode Current ◽  
Si3n4 Matrix ◽  
Effect Of The Composition

A nanocomposite CrAlSiN–AlSiN coating with periodically modulated composition was developed and investigated regarding the effect of the composition and structure on the mechanical properties. The modulation was performed by variation of the pressure, cathode current and bias voltage during deposition. The structure and composition of the coating were investigated by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS) analyses. The coating had a nanocomposite structure consisting of (CrAl)N and (AlSi)N nanograins embedded in a Si3N4 matrix. The EDS analysis of the cross-section revealed that the period composition had changed from Cr051Al0.41Si0.08N to Al0.82Cr0.04Si0.14N. It was shown that the elastic modulus could be adjusted by composition modulation. The coating hardness of 54 GPa was obtained by nanoindentation. The modulated CrAlSiN–AlSiN coating exhibited improved elastic strain to failure (H/E* = 0.11, H—nanohardness, E*—the effective elastic modulus), excellent resistance to plastic deformation (H3/E*2 = 0.72), and elastic recovery of 70%, which suggested improved toughness.

ROOM TEMPERATURE PHOTOLUMINESCENCE OF POLYCRYSTALLINE SIC PREPARED FROM CARBON-SATURATED SI MELT

2002 ◽  
Vol 16 (06n07) ◽  
pp. 1047-1051
Author(s):  
JIANPING MA ◽  
ZHIMING CHEN ◽  
GANG LU ◽  
MINGBIN YU ◽  
LIANMAO HANG ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Uv Light ◽  
X Ray Diffraction ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Composition And Structure ◽  
Light Excitation ◽  
Scanning Electron

Intense photoluminescence (PL) has been observed at room temperature from the polycrystalline SiC samples prepared from carbon-saturated Si melt at a temperature ranging from 1500 to 1650°C. Composition and structure of the samples have been confirmed by means of X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. PL measurements with 325 nm UV light excitation revealed that the room temperature PL spectrum of the samples consists of 3 luminescent bands, the peak energies of which are 2.38 eV, 2.77 eV and 3.06 eV, respectively. The 2.38 eV band is much stronger than the others. It is suggested that some extrinsic PL mechanisms associated with defect or interface states would be responsible to the intensive PL observed at room temperature.

Adaptive Nanocomposite Films Exhibiting Low Friction in a Broad Temperature Range

2005 ◽  
Author(s):  
C. Muratore ◽  
A. A. Voevodin ◽  
J. J. Hu ◽  
J. S. Zabinski
Keyword(s):  
Photoelectron Spectroscopy ◽  
Multilayer Film ◽  
Solid Lubricants ◽  
Deposition Process ◽  
Nanocomposite Films ◽  
X Ray Diffraction ◽  
Low Friction ◽  
X Ray ◽  
Composition And Structure ◽  
Different Temperatures

A hybrid magnetron sputtering/pulsed laser deposition process was used to grow nanocrystalline yttria stabilized zirconia (YSZ) embedded in an amorphous YSZ/metal matrix. This nanocomposite design reduced friction and improved the toughness of YSZ. Films containing both silver and molybdenum exhibited friction coefficients between 0.2 and 0.4 in air (40% relative humidity) against silicon nitride balls at temperatures between 25° C and 700 °C. Additional solid lubricants reduced the friction coefficient to <0.2 for over 10000 cycles at all temperatures. A multilayer film architecture was developed to further enhance the lifetime of the adaptive coatings. Electron microscopy, x-ray diffraction and x-ray photoelectron spectroscopy were used to correlate adaptive behavior at different temperatures to the composition and structure of the films.

Fabrication of Microporous Apatite Coating on Titanium by a Novel Chemical Method

2005 ◽  
Vol 284-286 ◽  
pp. 231-234
Author(s):  
Bo Feng ◽  
Jie Weng ◽  
Shao Xing Qu ◽  
Xing Dong Zhang
Keyword(s):  
Calcium Phosphate ◽  
Photoelectron Spectroscopy ◽  
Chemical Method ◽  
Carbonate Apatite ◽  
X Ray Diffraction ◽  
Energy Dispersion Spectroscopy ◽  
X Ray ◽  
Composition And Structure ◽  
Microporous Coating ◽  
Apatite Coating

A microporous apatite coating was fabricated by a heat-oxidation and chemical routine. The morphology, composition and structure were characterized by scanning electron microscopy with X-ray energy dispersion spectroscopy, X-ray photoelectron spectroscopy and X-ray diffraction. The components of the coating were predominantly apatite, next tri-calcium phosphate and octa-calcium phosphate. The pore size ranged from 1µm to5µm. The thickness of the coating was about 6µm ~ 10µm. The microporous coating was Ca-deficient carbonate apatite.

Formation of Titanium Dioxide Containing Calcium Phosphate Crystallites: A New Process

1995 ◽  
Vol 414 ◽  
Author(s):  
Laurent-Dominique Piveteau ◽  
Louis Schlapbach ◽  
Beat Gasser
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Titanium Dioxide ◽  
Chemical Composition ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Composition And Structure ◽  
New Process ◽  
Scanning Electron

AbstractA method for producing titanium dioxide (TiO2) containing hydroxyapatite (HA) crystallite isproposed. Solutions of CaCI2+H3PO4 and TiCL4+HCI combined with KOH are used to precipitatefirst the HA and then the TiO2.The precipitate is then sintered between 900°C and 1000°C for 18 to48 hours. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Energy DispersiveX-ray Analysis (EDX) and scanning electron microscopy (SEM) have been used to determine thecrystallinity, the chemical composition and structure of the samples.

Synthesis and characterization of fluorescein-grafted polyurethane for potential application in biomedical tracing

2016 ◽  
Vol 31 (6) ◽  
pp. 901-910 ◽  
Author(s):  
Boyuan Yang ◽  
Qin Zou ◽  
Lili Lin ◽  
Limei Li ◽  
Yi Zuo ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Composition And Structure ◽  
Fluorescence Efficiency ◽  
Fluorescence Characteristics ◽  
Fluorescent Response ◽  
Magnetic Resonance Scanning

Redesigned multifunctional biopolymers represent a novel building bridge for interdisciplinary collaborations in biomaterials development. We prepared fluorescein-grafted polyurethane scaffolds (PU-C1, PU-C5, and PU-B1) to meet both clinical needs and biological safety evaluations, using different contents of calcein and different synthesis procedures for potential biomedical tracing. X-ray diffraction, infrared, X-ray photoelectron spectroscopy, nuclear magnetic resonance, scanning electron microscopy, and light microscopy were used to analyze the composition and structure of polyurethanes, as well as to observe their morphology with and without biomarkers. Fluorescence spectrophotometer and fluorescence microscopy were used to detect the fluorescence characteristics. The results showed that the grafting of calcein significantly affected the chemical structure and fluorescence sensitivities of copolymers. When compared to calcein, which was added before synthesis (PU-C1), the marker that was added during the extender process (PU-B1) presented higher fluorescence efficiency. Both PU-C5 and PU-B1 exhibited strong fluorescent response and good cytocompatibility in vitro and in vivo, with no interference from the autofluorescence of tissues after 4 weeks of implantation. The fluorescence-marked material can be used to continuously and noninvasively monitor the dynamic changes in polymers, which provides a way to clearly trace the material or to distinguish between the material and tissue in vivo.

Investigation of the Effect of Uv-Assisted Oxidation and Nitridation of Hafnium Metal Films

2003 ◽  
Vol 780 ◽  
Author(s):  
C. Essary ◽  
V. Craciun ◽  
J. M. Howard ◽  
R. K. Singh
Keyword(s):  
Uv Radiation ◽  
Photoelectron Spectroscopy ◽  
Grazing Angle ◽  
X Ray Diffraction ◽  
Metal Thin Films ◽  
X Ray ◽  
Force Microscopy ◽  
Si Substrates ◽  
Atomic Force ◽  
Silicon Interface

AbstractHf metal thin films were deposited on Si substrates using a pulsed laser deposition technique in vacuum and in ammonia ambients. The films were then oxidized at 400 °C in 300 Torr of O2. Half the samples were oxidized in the presence of ultraviolet (UV) radiation from a Hg lamp array. X-ray photoelectron spectroscopy, atomic force microscopy, and grazing angle X-ray diffraction were used to compare the crystallinity, roughness, and composition of the films. It has been found that UV radiation causes roughening of the films and also promotes crystallization at lower temperatures.Furthermore, increased silicon oxidation at the interface was noted with the UVirradiated samples and was shown to be in the form of a mixed layer using angle-resolved X-ray photoelectron spectroscopy. Incorporation of nitrogen into the film reduces the oxidation of the silicon interface.

scholarly journals α-Cellulose Fibers of Paper-Waste Origin Surface-Modified with Fe3O4 and Thiolated-Chitosan for Efficacious Immobilization of Laccase

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 581
Author(s):  
Gajanan S. Ghodake ◽  
Surendra K. Shinde ◽  
Ganesh D. Saratale ◽  
Rijuta G. Saratale ◽  
Min Kim ◽  
...  
Keyword(s):  
Enzyme Immobilization ◽  
Photoelectron Spectroscopy ◽  
Cellulose Fibers ◽  
Relative Activity ◽  
Significant Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Laccase Immobilization ◽  
Surface Modified

The utilization of waste-paper-biomass for extraction of important α-cellulose biopolymer, and modification of extracted α-cellulose for application in enzyme immobilization can be extremely vital for green circular bio-economy. Thus, in this study, α-cellulose fibers were super-magnetized (Fe3O4), grafted with chitosan (CTNs), and thiol (-SH) modified for laccase immobilization. The developed material was characterized by high-resolution transmission electron microscopy (HR-TEM), HR-TEM energy dispersive X-ray spectroscopy (HR-TEM-EDS), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) analyses. Laccase immobilized on α-Cellulose-Fe3O4-CTNs (α-Cellulose-Fe3O4-CTNs-Laccase) gave significant activity recovery (99.16%) and laccase loading potential (169.36 mg/g). The α-Cellulose-Fe3O4-CTNs-Laccase displayed excellent stabilities for temperature, pH, and storage time. The α-Cellulose-Fe3O4-CTNs-Laccase applied in repeated cycles shown remarkable consistency of activity retention for 10 cycles. After the 10th cycle, α-Cellulose-Fe3O4-CTNs possessed 80.65% relative activity. Furthermore, α-Cellulose-Fe3O4-CTNs-Laccase shown excellent degradation of pharmaceutical contaminant sulfamethoxazole (SMX). The SMX degradation by α-Cellulose-Fe3O4-CTNs-Laccase was found optimum at incubation time (20 h), pH (3), temperatures (30 °C), and shaking conditions (200 rpm). Finally, α-Cellulose-Fe3O4-CTNs-Laccase gave repeated degradation of SMX. Thus, this study presents a novel, waste-derived, highly capable, and super-magnetic nanocomposite for enzyme immobilization applications.

scholarly journals Photocatalytic Reduction of CO2 to Methanol Using a Copper-Zirconia Imidazolate Framework

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 346
Author(s):  
Sonam Goyal ◽  
Maizatul Shima Shaharun ◽  
Ganaga Suriya Jayabal ◽  
Chong Fai Kait ◽  
Bawadi Abdullah ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Catalyst Support ◽  
Oxidation Potential ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molar Ratios ◽  
Optimum Parameters ◽  
Reduction Of Co2 ◽  
Enhanced Yield

A set of novel photocatalysts, i.e., copper-zirconia imidazolate (CuZrIm) frameworks, were synthesized using different zirconia molar ratios (i.e., 0.5, 1, and 1.5 mmol). The photoreduction process of CO2 to methanol in a continuous-flow stirred photoreactor at pressure and temperature of 1 atm and 25 °C, respectively, was studied. The physicochemical properties of the synthesized catalysts were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The highest methanol activity of 818.59 µmol/L.g was recorded when the CuZrIm1 catalyst with Cu/Zr/Im/NH4OH molar ratio of 2:1:4:2 (mmol/mmol/mmol/M) was employed. The enhanced yield is attributed to the presence of Cu2+ oxidation state and the uniformly dispersed active metals. The response surface methodology (RSM) was used to optimize the reaction parameters. The predicted results agreed well with the experimental ones with the correlation coefficient (R2) of 0.99. The optimization results showed that the highest methanol activity of 1054 µmol/L.g was recorded when the optimum parameters were employed, i.e., stirring rate (540 rpm), intensity of light (275 W/m2) and photocatalyst loading (1.3 g/L). The redox potential value for the CuZrIm1 shows that the reduction potential is −1.70 V and the oxidation potential is +1.28 V for the photoreduction of CO2 to methanol. The current work has established the potential utilization of the imidazolate framework as catalyst support for the photoreduction of CO2 to methanol.

scholarly journals Study on the Electrical, Structural, Chemical and Optical Properties of PVD Ta(N) Films Deposited with Different N2 Flow Rates

Coatings ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 937
Author(s):  
Yingying Hu ◽  
Md Rasadujjaman ◽  
Yanrong Wang ◽  
Jing Zhang ◽  
Jiang Yan ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Optical Properties ◽  
Photoelectron Spectroscopy ◽  
Crystal Size ◽  
Silicon Substrates ◽  
X Ray Diffraction ◽  
Dc Magnetron Sputtering ◽  
Flow Rates ◽  
X Ray ◽  
N2 Flow Rate

By reactive DC magnetron sputtering from a pure Ta target onto silicon substrates, Ta(N) films were prepared with different N2 flow rates of 0, 12, 17, 25, 38, and 58 sccm. The effects of N2 flow rate on the electrical properties, crystal structure, elemental composition, and optical properties of Ta(N) were studied. These properties were characterized by the four-probe method, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and spectroscopic ellipsometry (SE). Results show that the deposition rate decreases with an increase of N2 flows. Furthermore, as resistivity increases, the crystal size decreases, the crystal structure transitions from β-Ta to TaN(111), and finally becomes the N-rich phase Ta3N5(130, 040). Studying the optical properties, it is found that there are differences in the refractive index (n) and extinction coefficient (k) of Ta(N) with different thicknesses and different N2 flow rates, depending on the crystal size and crystal phase structure.

scholarly journals Optical, XPS and XRD Studies of Semiconducting Copper Sulfide Layers on a Polyamide Film

2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Valentina Krylova ◽  
Mindaugas Andrulevičius
Keyword(s):  
Photoelectron Spectroscopy ◽  
Copper Sulfide ◽  
Diffusion Method ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Xrd Studies ◽  
Polyamide Film ◽  
Indirect Band Gap ◽  
Xrd Method

Copper sulfide layers were formed on polyamide PA 6 surface using the sorption-diffusion method. Polymer samples were immersed for 4 and 5 h in 0.15 mol⋅  solutions and acidified with HCl (0.1 mol⋅) at . After washing and drying, the samples were treated with Cu(I) salt solution. The samples were studied by UV/VIS, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) methods. All methods confirmed that on the surface of the polyamide film a layer of copper sulfide was formed. The copper sulfide layers are indirect band-gap semiconductors. The values of are 1.25 and 1.3 eV for 4 h and 5 h sulfured PA 6 respectively. Copper XPS spectra analyses showed Cu(I) bonds only in deeper layers of the formed film, while in sulfur XPS S 2p spectra dominating sulfide bonds were found after cleaning the surface with ions. It has been established by the XRD method that, beside , the layer contains as well. For PA 6 initially sulfured 4 h, grain size forchalcocite, , was  nm and fordjurleite, , it was 54.17 nm. The sheet resistance of the obtained layer varies from 6300 to 102 .

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