scholarly journals Fabrication of TiO2Crystalline Coatings by Combining Ti-6Al-4V Anodic Oxidation and Heat Treatments

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
María Laura Vera ◽  
Mario Roberto Rosenberger ◽  
Carlos Enrique Schvezov ◽  
Alicia Esther Ares

The bio- and hemocompatibility of titanium alloys are due to the formation of a TiO2layer. This natural oxide may have fissures which are detrimental to its properties. Anodic oxidation is used to obtain thicker films. By means of this technique, at low voltages oxidation, amorphous and low roughness coatings are obtained, while, above a certain voltage, crystalline and porous coatings are obtained. According to the literature, the crystalline phases of TiO2, anatase, and rutile would present greater biocompatibility than the amorphous phase. On the other hand, for hemocompatible applications, smooth and homogeneous surfaces are required. One way to obtain crystalline and homogeneous coatings is by heat treatments after anodic oxidation. The aim of this study is to evaluate the influence of heat treatments on the thickness, morphology, and crystalline structure of the TiO2anodic coatings. The characterization was performed by optical and scanning electron microscopy, X-ray diffraction, and X-ray reflectometry. Coatings with different colors of interference were obtained. There were no significant changes in the surface morphology and roughness after heat treatment of 500°C. Heat treated coatings have different proportions of the crystalline phases, depending on the voltage of anodic oxidation and the temperature of the heat treatment.

2007 ◽  
Vol 336-338 ◽  
pp. 1829-1832 ◽  
Author(s):  
Qing Bo Tian ◽  
Yue Wang ◽  
Xue Tao Yue ◽  
Yan Sheng Yin ◽  
Su Hua Fan

The phase-separation and the crystallization of SiO2-MgO-Al2O3-K2O-Fe2O3-F glass were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and electron probe of microanalyzers (EPMA). The results reveal that the varieties and the morphology of crystalline phases formed depend sensitively on the thermal treatment schedules. During the isothermal treatments, the crystalline phases of mica, mica and iron oxide (FeFeO4), and FeFeO4 as major crystals are precipitated in the glass samples heat-treated at 900, 1000 and 1050°C respectively. However, the two-step heat treatment beginning at 900°C for 1h and subsequently followed at 1050°C for 1h leads to the precipitation of mica crystal and no any signs of FeFeO4 crystalline phase is observed. Also the morphology of sample is different from that of the isothermally treated glass at 1050°C, but is similar from that of sample at 900°C. A “worm”-shaped phase-separation is observed in the sample heated at 800°C for 0.5h, which exhibits different morphology from that of droplet- or globule-shape conventionally discerned. EPMA results show that the incorporation of Fe2O3 accelerates accumulation of fluorine element, promoting the phase-separation and the crystallization of the present glass.


2011 ◽  
Vol 687 ◽  
pp. 474-479
Author(s):  
Kun Peng Zhu ◽  
Ning Hu ◽  
Fu Shun Liu

The influence of Fe addition on the phase transformation and the microstructure of Cu67Al27-XMn6FeXshape memory alloys are investigated by means of electrical resistivity, X-ray diffraction, scanning electron microscopy and microhardness test. It was shown that the Ms (Martensitic start transformation) temperature of the 850°C heat-treated alloy exhibit a sharp increase as Fe content increases, by comparison with the alloy without heat-treatment. For example, after 850°C heat-treatment, the Ms temperature of the alloy increases from 52K to 135K when Fe is added from 0 at.% to 1.5 at.%. The microstructure of as-homogenized Cu67Al27-XMn6FeXalloys consists of Cu3Al matrix, γ2(Cu9Al4) and α (Cu) phases. Fe element was distributed in precipitates and matrix.


1989 ◽  
Vol 4 (5) ◽  
pp. 1093-1098 ◽  
Author(s):  
Ira Bloom ◽  
B. S. Tani ◽  
M. C. Hash ◽  
Donglu Shi ◽  
M. A. Patel ◽  
...  

Two YBa2Cu3O7−x powders were investigated: one was nearly stoichiometric, and the other, CuO-rich. After being sintered at 950 °C, samples from both powders were heat-treated in oxygen at 845, 860, and 910 °C for up to 10 days. The samples were characterized by differential thermal analysis, x-ray diffraction, optical and scanning electron microscopy, iodometric titrations, and measurement of their superconducting properties (electrical resistivity, critical temperature, and critical current density). The electrical properties of the nearly stoichiometric material improved with time at all temperatures. On the other hand, the electrical properties of the CuO-rich material deteriorated with temperature, possibly owing to problems associated with grain growth at 910 °C.


2005 ◽  
Vol 288-289 ◽  
pp. 215-218 ◽  
Author(s):  
Qi Feng Yu ◽  
Bang Cheng Yang ◽  
Yao Wu ◽  
Xing Dong Zhang

In this study, alkali-heat treatment in NaOH solution and heat treatment, which could form amorphous sodium titanate on nanophase titania ceramics surface by conditioning the process, was employed to modify the structure and bioactivity of biomedical titania ceramics. After the nanophase titania ceramics was subjected to alkali-heat treatment, thin film X-ray diffraction and scanning electron microscopy results showed the titania ceramics surfaces were covered by porous sodium titanate. In fast calacification solution (FCS), the alkali-heat treated titania ceramics could induce bonelike apatite formation on its surface. Our results showed that induction of apatite-forming ability on titania ceramics could be attained by alkali-heat treatment. So it was an effective way to prepare bioactive titania ceramics by combining sintering and alkali-heat treatment.


2009 ◽  
Vol 283-286 ◽  
pp. 268-272 ◽  
Author(s):  
S. Cihangir ◽  
Celaletdin Ergun ◽  
Suat Yılmaz ◽  
Filiz Çinar Şahin

In the present study, a method based on sulfuric acid dehydration of sugar was developed to synthesize a precursor material, which can yield B4C/SiC composites at much lower temperatures compared to traditional carbothermal methods. The precursor material for pure B4C was heat treated at the temperatures between 400 and 1600oC under inert atmosphere. The precursor material for B4C /SiC composites was heat treated only at 1600oC under an inert atmosphere. Then the samples were characterized by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The results showed that B-C bonds formed as low as 400oC. On the other hand, crystallized B4C and B4C / SiC composites can be obtained at the heat treatment temperatures between 1400 and 1600oC.


2010 ◽  
Vol 660-661 ◽  
pp. 302-307
Author(s):  
P.B. Santos ◽  
S.C. Silva ◽  
Rubens Nunes de Faria Jr. ◽  
Hidetoshi Takiishi

The first goal of this work involved the study of the effect of variables the HDDR processing, such as: the added pressure of H2 in the system, the time of heat treatment and recombination of Pr12Fe65.9Co16B6Nb0.1 alloy with the aim of improving the magnetic properties like the magnetic properties of the Pr14Fe63.9Co16B6Nb0.1 alloy (Br= 865mT and iHc= 790mT). The second aim of the work involved the characterization of HDDR powders that were analyzed by X-ray diffraction for identification and quantification of crystalline phases. These materials were analyzed by scanning electron microscopy (SEM).


2021 ◽  
Author(s):  
Mei Yang ◽  
Yishu Zhang ◽  
Haoxing You ◽  
Richard Smith ◽  
Richard D. Sisson

Abstract Selective laser melting (SLM) is an additive manufacturing technique that can be used to make the near-net-shape metal parts. M2 is a high-speed steel widely used in cutting tools, which is due to its high hardness of this steel. Conventionally, the hardening heat treatment process, including quenching and tempering, is conducted to achieve the high hardness for M2 wrought parts. It was debated if the hardening is needed for additively manufactured M2 parts. In the present work, the M2 steel part is fabricated by SLM. It is found that the hardness of as-fabricated M2 SLM parts is much lower than the hardened M2 wrought parts. The characterization was conducted including X-ray diffraction (XRD), optical microscopy, Scanning Electron Microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS) to investigate the microstructure evolution of as-fabricated, quenched, and tempered M2 SLM part. The M2 wrought part was heat-treated simultaneously with the SLM part for comparison. It was found the hardness of M2 SLM part after heat treatment is increased and comparable to the wrought part. Both quenched and tempered M2 SLM and wrought parts have the same microstructure, while the size of the carbides in the wrought part is larger than that in the SLM part.


2017 ◽  
Vol 62 (2) ◽  
pp. 1005-1010 ◽  
Author(s):  
Peyala Dharmaiah ◽  
C.H. Lee ◽  
B. Madavali ◽  
Soon-Jik Hong

AbstractIn the present work, we have prepared Bi2Te3nanostructures with different morphologies such as nano-spherical, nanoplates and nanoflakes obtained using various surfactant additions (EG, PVP, and EDTA) by a hydrothermal method. The shape of the nanoparticles can be controlled by addition of surfactants. The samples were characterized by x-ray diffraction (XRD) and scanning electron microscopy (SEM). It is found that the minority BiOCl phase disappears after maintained pH at 10 with EG as surfactant. SEM bulk microstructure reveals that the sample consists of fine and coarse grains. Temperature dependence of thermoelectric properties of the nanostructured bulk sample was investigated in the range of 300-450K. The presence of nanograins in the bulk sample exhibits a reduction of thermal conductivity and less effect on electrical conductivity. As a result, a figure of merit of the sintered bulk sample reached 0.2 at 400 K. A maximum micro Vickers hardness of 102 Hv was obtained for the nanostructured sample, which was higher than the other reported results.


2021 ◽  
Vol 234 ◽  
pp. 00106
Author(s):  
Houda Labjar ◽  
Hassan Chaair

The synthesis of apatite silicated Ca10(PO4)6-x(SiO4)x(OH)2-x (SiHA) with 0≤x≤2 was investigated using a wet precipitation method followed by heat treatment using calcium carbonate CaCO3 and phosphoric acid H3PO4 and silicon tetraacetate SiC8H20O4 (TEOS) in medium of water ethanol, with three different silicate concentrations. After drying, the samples are ground and then characterized by different analytical techniques like X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron Microscopy (SEM) and chemical analysis.


2018 ◽  
Vol 25 (08) ◽  
pp. 1950023 ◽  
Author(s):  
ARKADEB MUKHOPADHYAY ◽  
TAPAN KUMAR BARMAN ◽  
PRASANTA SAHOO

The present work reports the deposition of a quaternary Ni-B-W-Mo coating on AISI 1040 medium carbon steel and its characterization. Quaternary deposits are obtained by suitably modifying existing electroless Ni-B bath. Composition of the as-deposited coating is analyzed by energy dispersive X-ray spectroscopy. The structural aspects of the as-deposited and coatings heat treated at 300[Formula: see text]C, 350[Formula: see text]C, 400[Formula: see text]C, 450[Formula: see text]C and 500[Formula: see text]C are determined using X-ray diffraction technique. Surface of the as-deposited and heat-treated coatings is examined using a scanning electron microscope. Very high W deposition could be observed when sodium molybdate is present in the borohydride-based bath along with sodium tungstate. The coatings in their as-deposited condition are amorphous while crystallization takes place on heat treatment. A nodulated surface morphology of the deposits is also observed. Vickers’ microhardness and crystallite size measurement reveal inclusion of W and Mo results in enhanced thermal stability of the coatings. Solid solution strengthening of the electroless coatings by W and Mo is also observed. The applicability of kinetic strength theory to the hardening of the coatings on heat treatment is also investigated. Corrosion resistance of Ni-B-W-Mo coatings and effect of heat treatment on the same are also determined by electrochemical techniques.


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