Production and wear property of electroless Ni-plated B4C-AstaloyCr-M composites

2015 ◽  
Vol 22 (3) ◽  
pp. 251-255
Author(s):  
Ahmet Yonetken ◽  
Şükrü Talaş ◽  
Ayhan Erol ◽  
Ömer Gökoğlan ◽  
Taner Mersin
Keyword(s):  
Xrd Analysis ◽  
Wear Property ◽  
X Ray Diffraction ◽  
Ceramic Phase ◽  
X Ray ◽  
Conventional Furnace ◽  
Sem Study ◽  
Furnace Sintering ◽  
Compressive Testing ◽  
Electroless Ni

AbstractNickel (Ni) matrix reinforced with boron carbide (B4C) has been produced by conventional furnace sintering at various temperatures. A uniform Ni layer on B4C powders was deposited prior to sintering using electroless plating technique, allowing close surface contact between particles. A composite consisting of quaternary additions, a ceramic phase, B4C, within a matrix of Ni and AstaloyCr-M powders has been prepared at a temperature range of 1000°C–1200°C under Ar shroud. X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM) study, compressive testing, and hardness measurements were employed to characterize the properties of the composite. Experimental results showed that the best properties as compressive strength σmax and hardness (HB) were obtained at 1150°C. Wear resistance was relatively higher than cast iron.

Identification of acid-insoluble filter-plugging compounds and optimal acid-washing procedures for tubular backpulse pressure filters

TAPPI Journal ◽  
2011 ◽  
Vol 10 (1) ◽  
pp. 17-23
Author(s):  
KEVIN TAYLOR ◽  
RICH ADDERLY ◽  
GAVIN BAXTER
Keyword(s):  
Calcium Sulfate ◽  
Membrane Filter ◽  
Sulfamic Acid ◽  
Xrd Analysis ◽  
Metal Sulfides ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gypsum Formation ◽  
Acid Washing ◽  
Hydrolysis Of

Over time, performance of tubular backpulse pressure filters in kraft mills deteriorates, even with regular acid washing. Unscheduled filter replacement due to filter plugging results in significant costs and may result in mill downtime. We identified acid-insoluble filter-plugging materials by scanning electron microscope/energy-dispersion X-ray spectroscopy (SEM/EDS) and X-ray diffraction (XRD) analysis in both polypropylene and Gore-Tex™ membrane filter socks. The major filter-plugging components were calcium sulfate (gypsum), calcium phosphate (hydroxylapatite), aluminosilicate clays, metal sulfides, and carbon. We carried out detailed sample analysis of both the standard acid-washing procedure and a modified procedure. Filter plugging by gypsum and metal sulfides appeared to occur because of the acid-washing procedure. Gypsum formation on the filter resulted from significant hydrolysis of sulfamic acid solution at temperatures greater than 130°F. Modification of the acid-washing procedure greatly reduced the amount of gypsum and addition of a surfactant to the acid reduced wash time and mobilized some of the carbon from the filter. With surfactant, acid washing was 95% complete after 40 min.

A study on using expanded perlite with hydroxyapatite: Reinforced bio-composites

2021 ◽  
pp. 095441192199656
Author(s):  
Erdoğan Karip ◽  
Mehtap Muratoğlu
Keyword(s):  
Body Fluid ◽  
Xrd Analysis ◽  
Cold Isostatic Pressing ◽  
Expanded Perlite ◽  
X Ray Diffraction ◽  
Pressing Method ◽  
X Ray ◽  
Infra Red ◽  
Ft Ir

People are exposed to different kinds of diseases or various accidents in life. Hydroxyapatite (HA) has been widely employed for bone treatment applications. In this study, HA was extracted from sheep bones. Bio-composites were doped with 1, 5, and 10 wt.% of expanded perlite and 5 wt.% of ZrO2–MgO-P2O5. The bio-composites were prepared by the cold isostatic pressing method (250 MPa) and sintered at 900°C for 1 h. In order to evaluate the characteristics of the bio-composites, microhardness, density, X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) analyses were carried out on them. Additionally, the specimens whose characteristics were determined were kept in synthetic body fluid (SBF), and their in vitro behavior was examined. As a result, it was observed that microhardness increased as both the weight and the grain size of the expanded perlite were increased. Calcium silicate, tri-calcium phosphate, and hydroxyapatite were observed in the XRD analysis of all samples, and the formation of apatite structures was increased by addition of ZrO2–MgO–P2O5.

scholarly journals An Insight into Chemistry and Structure of Colloidal 2D-WS2 Nanoflakes: Combined XPS and XRD Study

Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1969
Author(s):  
Riccardo Scarfiello ◽  
Elisabetta Mazzotta ◽  
Davide Altamura ◽  
Concetta Nobile ◽  
Rosanna Mastria ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Xrd Analysis ◽  
Crystal Habit ◽  
Phase Identification ◽  
X Ray Diffraction ◽  
X Ray ◽  
Morphological Evaluation ◽  
Rational Understanding ◽  
Structural Inspection

The surface and structural characterization techniques of three atom-thick bi-dimensional 2D-WS2 colloidal nanocrystals cross the limit of bulk investigation, offering the possibility of simultaneous phase identification, structural-to-morphological evaluation, and surface chemical description. In the present study, we report a rational understanding based on X-ray photoelectron spectroscopy (XPS) and structural inspection of two kinds of dimensionally controllable 2D-WS2 colloidal nanoflakes (NFLs) generated with a surfactant assisted non-hydrolytic route. The qualitative and quantitative determination of 1T’ and 2H phases based on W 4f XPS signal components, together with the presence of two kinds of sulfur ions, S22− and S2−, based on S 2p signal and related to the formation of WS2 and WOxSy in a mixed oxygen-sulfur environment, are carefully reported and discussed for both nanocrystals breeds. The XPS results are used as an input for detailed X-ray Diffraction (XRD) analysis allowing for a clear discrimination of NFLs crystal habit, and an estimation of the exact number of atomic monolayers composing the 2D-WS2 nanocrystalline samples.

scholarly journals Effect of Molybdenum Content on the Corrosion and Microstructure of Low-Ni, Co-Free Maraging Steels

Metals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 852
Author(s):  
Asiful H. Seikh ◽  
Hossam Halfa ◽  
Mahmoud S. Soliman
Keyword(s):  
Corrosion Resistance ◽  
Electrochemical Impedance ◽  
Microstructural Analysis ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Alloying Element ◽  
X Ray ◽  
Maraging Steels ◽  
Eds Analysis ◽  
Electroslag Refining

Molybdenum (Mo) is an important alloying element in maraging steels. In this study, we altered the Mo concentration during the production of four cobalt-free maraging steels using an electroslag refining process. The microstructure of the four forged maraging steels was evaluated to examine phase contents by optical microscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD) analysis. Additionally, we assessed the corrosion resistance of the newly developed alloys in 3.5% NaCl solution and 1 M H2SO4 solution through potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques. Furthermore, we performed SEM and energy-dispersive spectroscopy (EDS) analysis after corrosion to assess changes in microstructure and Raman spectroscopy to identify the presence of phases on the electrode surface. The microstructural analysis shows that the formation of retained austenite increases with increasing Mo concentrations. It is found from corrosion study that increasing Mo concentration up to 4.6% increased the corrosion resistance of the steel. However, further increase in Mo concentration reduces the corrosion resistance.

scholarly journals Microscopic study of zinc nanoparticles synthesised using thermosetting polymer

2019 ◽  
Vol 49 (1) ◽  
Author(s):  
Giriraj Tailor ◽  
Jyoti Chaudhay ◽  
Deepshikha Verma ◽  
Bhupendra Kr. Sarma
Keyword(s):  
Electron Microscope ◽  
Xrd Analysis ◽  
The Novel ◽  
X Ray Diffraction ◽  
Zinc Nanoparticles ◽  
Transmission Electron ◽  
Sem Study ◽  
Zinc Salts ◽  
Thermosetting Polymer ◽  
Low Crystalline

AbstractThe present study reports the novel synthesis of Zinc nanoparticles (Zn NPs) by thermal decomposition method and its characterisation by Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM), and X-ray Diffraction Measurements (XRD). Synthesis of Zn NPs was achieved by using thermosetting polymer and zinc salts as precursor. Zn NPs were obtained on calcination at 850 °C for 30 min. SEM study reveals that synthesized nanoparticles are spherical in shape. XRD analysis shows that the Zn NPs formed are low crystalline in nature.

Characterization and A Preliminary Study of TiO2 Synthesis from Lampung Iron Sand

2020 ◽  
Vol 849 ◽  
pp. 113-118
Author(s):  
Yayat Iman Supriyatna ◽  
Slamet Sumardi ◽  
Widi Astuti ◽  
Athessia N. Nainggolan ◽  
Ajeng W. Ismail ◽  
...  
Keyword(s):  
Food Packaging ◽  
Xrd Analysis ◽  
Major Elements ◽  
Raw Material ◽  
Solid Residue ◽  
X Ray Diffraction ◽  
X Ray ◽  
Leaching Solution ◽  
Ti Content

The purpose of this study is to characterize Lampung iron sand and to conduct preliminary experiments on the TiO2 synthesis which can be used for the manufacturing of functional food packaging. The iron sand from South Lampung Regency, Lampung Province that will be utilized as raw material. The experiment was initiated by sieving the iron sand on 80, 100, 150, 200 and 325 mesh sieves. Analysis using X-Ray Fluorescence (XRF) to determine the element content and X-Ray Diffraction (XRD) to observe the mineralization of the iron sand was conducted. The experiment was carried out through the stages of leaching, precipitation, and calcination. Roasting was applied firstly by putting the iron sand into the muffle furnace for 5 hours at a temperature of 700°C. Followed by leaching using HCl for 48 hours and heated at 105°C with a stirring speed of 300 rpm. The leaching solution was filtered with filtrate and solid residue as products. The solid residue was then leached using 10% H2O2 solution. The leached filtrate was heated at 105°C for 40 minutes resulting TiO2 precipitates (powder). Further, the powder was calcined and characterized. Characterization of raw material using XRF shows the major elements of Fe, Ti, Mg, Si, Al and Ca. The highest Ti content is found in mesh 200 with 9.6%, while iron content is about 80.7%. While from the XRD analysis, it shows five mineral types namely magnetite (Fe3O4), Rhodonite (Mn, Fe, Mg, Ca) SiO3, Quart (SiO2), Ilmenite (FeOTiO2) and Rutile (TiO2). The preliminary experiment showed that the Ti content in the synthesized TiO2 powder is 21.2%. The purity of TiO2 is low due to the presence of Fe metal which is dissolved during leaching, so that prior to precipitation purification is needed to remove impurities such as iron and other metals.

THE SOLIDIFICATION MICROSTRUCTURE OF BIOMEDICAL TITANIUM ALLOYS UNDER THE CENTRIFUGAL FORCE

2006 ◽  
Vol 20 (25n27) ◽  
pp. 4685-4690
Author(s):  
ZIYONG CHEN ◽  
LIJUAN XU ◽  
ZHIGUANG LIU ◽  
YUYONG CHEN
Keyword(s):  
Centrifugal Force ◽  
Graphite Crucible ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Crystal Boundary ◽  
X Ray ◽  
Solidification Defects ◽  
Solidification Microstructures ◽  
Centrifugal Equipment ◽  
Graphite Mould

Two biomedical alloys, Ti -39 Nb -5.1 Ta -7.1 Zr ( TNTZ1 ) and Ti -35.3 Nb -5.1 Ta -7.1 Zr ( TNTZ2 ) were melted using LZ5 type centrifugal equipment for casting titanium. The solidification microstructures of TNTZ1 and TNTZ2 alloys cast in graphite crucible without centrifugal force are mostly big arborescent crystal with dispersed porosity in it. After pouring into a graphite mould under centrifugal force, the lower part of ingot showed mostly arborescent crystals with few equiaxed crystals, while the upper part of ingot is basically spherical equiaxed crystals. The solidification defects, such as dispersed pores were very difficult to find. Nb is supposed to refine the arborescent crystals. X-ray diffraction (XRD) analysis showed Ti -phase and Nb -phase existing in the above two alloys. The content of Ti was found relatively low in crystal interior and relatively high in crystal boundary. The content of Nb/Zr was uniform in whole microstructure.

Influence of High Current Pulsed Electron Beam Irradiation on Ni-P Electroless Plating

2011 ◽  
Vol 299-300 ◽  
pp. 77-81
Author(s):  
Yang Xu ◽  
Sheng Zhi Hao ◽  
Xiang Dong Zhang ◽  
Min Cai Li ◽  
Chuang Dong
Keyword(s):  
Electroless Plating ◽  
Electron Beam Irradiation ◽  
Xrd Analysis ◽  
High Current ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pulsed Electron Beam ◽  
6063 Aluminum Alloy ◽  
Pre Treatment ◽  
Better Than

The surface irradiation of 6063 aluminum alloy by high current pulsed electron was conducted with the aim of replacing the complicated pre-treatment in the processes of electroless plating. To explore the microstructure changes, optical metallography, SEM (scanning electron microscope), XRD (X-ray diffraction) analyses were carried out, and the sliding tests were used for the detection of wear resistance. It was concluded that the HCPEB irradiation could replace the pre-treatment of aluminum substrate as required in conventional electroless plating with a decreased surface roughness of Ni-P alloy plating layer. The plates exhibited an amorphous microstructure as demonstrated by XRD analysis. The plates, produced with the routine of HCPEB irradiation, activation and electroless plating possess, also exhibited good quality, even better than that of conventional electroless plating technique.

The Characteristic Evaluation of Hydroxyapatite Powders Synthesized from CaCO3 Refined from Oyster Shell and H3PO4

2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu
Keyword(s):  
Bone Density ◽  
Inductively Coupled Plasma ◽  
Oyster Shell ◽  
Atomic Emission ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled ◽  
Infra Red ◽  
Ft Ir

Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) powders is synthesized using the mixed powders of CaCO3 refined from oyster shells and phosphoric acid (H3PO4-98%, Daejung) as starting materials. The characteristic evaluation and chemical analysis of the synthesized powders is performed by X-ray diffraction (XRD), Fourier-transformed infra-red spectroscopy (FT-IR), and inductively-coupled plasma atomic emission spectroscopy (ICPAES). XRD analysis of synthetic powder by heat treatment at 1300°C for 2hrs shows only HAp peaks corresponding to stoichiometric HAp. It is confirmed by ICP-AES test that impurities such as Zn, In, Ti, Ba, Cd, Pb, and Mn, is not detected at all, but small amounts of Ti and Be is observed (0.099ppm Ti and 0.002ppm Ba). Variation of bone density is measured by giving medication of HAp powder with drinking water into human body continuously for three month. After the medication, the bone density is higher than the medication before. This means that HAp powder made from this process can be used as improver of bone density.

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