X-ray Diffraction Studies of the Axial Tensile Modulus of Rigid-Rod Polymer Fibers

1988 ◽  
Vol 134 ◽  
Author(s):  
P. Galen Lenhert ◽  
W. Wade Adams
Keyword(s):  
Tensile Modulus ◽  
Polymer Fibers ◽  
X Ray Diffraction ◽  
X Ray ◽  
Axial Tensile ◽  
Heat Treated ◽  
Before And After ◽  
Control Computer ◽  
Rigid Rod ◽  
Fiber Sample

ABSTRACTWe report the design and use of a device to measure the axial tensile modulus of high modulus fibers by following the change in the meridional X-ray spacings as a function of applied tension. The device, which mounts on a Picker 4-circle automated diffractometer, applies tension to the fiber sample by a cantilever arrangement. Tension is measured by a strain gauge bridge on the cantilever arm. The tension is adjusted and read by the control computer, a VAX 11/730. Measurements made on PBZT and PBO fibers before and after heat treatment are reported. For PBZT fibers (as spun, and heat treated at 525° C and 650° C) with tensile moduli of 186, 283 and 290 GPa, the X-ray determined moduli are 348, 385 and 395 GPa. For PBO fibers (as spun and heat treated at 600° C and 665° C) with tensile moduli of 166, 318 and 290 GPa, the X-ray determined moduli are 387, 477 and 433 GPa. These modulus values are to be compared with theoretical values presented by Wierschke in the previous paper and sonic modulus values discussed by Jiang et al in the following paper.

scholarly journals Ostrich eggshell as calcium source for the synthesis of hydroxyapatite and hydroxyapatite partially substituted with zinc

Cerâmica ◽  
2016 ◽  
Vol 62 (364) ◽  
pp. 386-391 ◽  
Author(s):  
J. R. M. Ferreira ◽  
L. H. L. Louro ◽  
A. M. Costa ◽  
J. B. de Campos ◽  
M. H. Prado da Silva
Keyword(s):  
Xrd Analysis ◽  
Quantitative Chemical Analysis ◽  
X Ray Diffraction ◽  
Spectroscopy Technique ◽  
X Ray ◽  
Heat Treated ◽  
Before And After ◽  
Calcium Source ◽  
The Fourier Transform ◽  
Ostrich Eggshell

Abstract In the present study, hydroxyapatite and Zn-substituted hydroxyapatite powders were synthesized using ostrich eggshell as a calcium source. The samples were analyzed by scanning electron microscopy with field emission gun, and X-ray diffraction (XRD) to identify the present phases, and X-ray fluorescence spectroscopy for quantitative chemical analysis of the synthesized and heat treated powders. The Fourier transform infrared spectroscopy technique was used before and after heat treatments at 700, 900 and 1100 °C in order to identify the functional groups present, as an additional technique to the XRD analysis. The results presented in this study represent a promising method for synthesis of hydroxyapatite and hydroxyapatite partially substituted with zinc, since the results showed no undesirable phases or impurities in the produced powders. It was observed that Zn-substituted hydroxyapatite showed higher thermal stability, when compared to pure hydroxyapatite.

Second-Generation Aluminium Extraction Residue Used as Devitrification Aid for Glass-Ceramics

2008 ◽  
Vol 587-588 ◽  
pp. 773-777
Author(s):  
M.C. Ferreira ◽  
Wilson Acchar ◽  
Ana M. Segadães ◽  
Sonia Regina Homem de Mello-Castanho
Keyword(s):  
Second Generation ◽  
Glass Ceramics ◽  
Glass Frit ◽  
Raw Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Before And After ◽  
Devitrification Process ◽  
Extraction Metallurgy

Brazil has one of the world’s most important Bauxite deposits, the raw material for the aluminium extraction metallurgy. This work is focused on finding a suitable application for the white dross residue (WDR), a second-generation waste material produced during the metal recovery from the slag left after the primary extraction of aluminium from the ore. A commercial lime-silica based glass frit was used, to which WDR additions were made (up to 30 wt.%), aimed at studying the devitrification process of the glasses produced. Such mixtures were melted at temperatures varying from 1100 to 1500°C and the resulting fritted glasses were heat treated at 900°C. The starting materials and the mixtures thereof were characterized before and after thermal treatment by differential thermal analysis, X-ray diffraction and fluorescence, and scanning electron microscopy. The results obtained showed that the WDR is easily incorporated into the glass matrix and causes easy devitrification after short heat treatment periods at low temperature.

Temperature-Controlled Devitrification of Oxyfluoride Borate Glasses

2007 ◽  
Vol 130 ◽  
pp. 263-266 ◽  
Author(s):  
Joanna Pisarska ◽  
Tomasz Goryczka ◽  
Wojciech A. Pisarski
Keyword(s):  
Heat Treatment ◽  
Glass Ceramics ◽  
Borate Glasses ◽  
X Ray Diffraction ◽  
Transparent Glass ◽  
X Ray ◽  
Heat Treated ◽  
Before And After ◽  
Controlled Crystallization ◽  
Temperature Controlled

Selected oxyfluoroborate glasses have been investigated before and after heat treatment. Transparent glass-ceramics (TGC) were obtained during controlled crystallization (devitrification). X-ray diffraction studies confirmed that material was partially crystallized. Diffraction lines due to orthorhombic PbF2 phase were identified for heat-treated samples at various temperatures and times. Results were compared to that ones obtained for as-melted glass.

scholarly journals Nanomechanical Behavior, Adhesion and Corrosion Resistance of Hydroxyapatite Coatings for Orthopedic Implant Applications

Coatings ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 477
Author(s):  
Kaouther Khlifi ◽  
Hafedh Dhiflaoui ◽  
Amir Ben Rhouma ◽  
Joël Faure ◽  
Hicham Benhayoune ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Corrosion Resistance ◽  
X Ray Diffraction ◽  
Homogeneous Microstructure ◽  
X Ray ◽  
Hydroxyapatite Coatings ◽  
Adhesion Behavior ◽  
Heat Treated ◽  
Before And After ◽  
Scratch Tests

The aim of this work was to investigate the nanomechanical, adhesion and corrosion resistance of hydroxyapatite (HAP) coatings. The electrodeposition process was used to elaborate the HAP coatings on Ti6Al4V alloy. The effect of hydrogen peroxide concentration H2O2 on the electrolyte and the heat treatment was studied. Surface morphology of HAP coatings was assessed, before and after heat treatment, by scanning electron microscopy associated with X-ray microanalysis (SEM-EDXS). Moreover, X-ray diffraction (XRD) was performed to identify the coatings’ phases and composition. Nanoindentation and scratch tests were performed for nanomechanical and adhesion behavior analysis. The corrosion resistance of the uncoated, the as-deposited, and the heat-treated coatings was investigated by electrochemical test. The obtained results revealed that, with 9% of H2O2 and after heat treatment, the HAP film exhibited a compact and homogeneous microstructure. The film also showed a crystal growth: stoichiometric hydroxyapatite (HAP) and β-tricalcium phosphate (β-TCP). After heat treatment, the nanomechanical properties (H, E) were increased from 117 ± 7 MPa and 24 ± 1 GPa to 171 ± 10 MPa and 38 ± 1.5 GPa respectively. Critical loads (LC1, LC2, and LC3) were increased from 0.78 ± 0.04, 1.6 ± 0.01, and 4 ± 0.23 N to 1.45 ± 0.08, 2.46 ± 0.14, and 4.35 ± 0.25 N (respectively). Furthermore, the adhesion strength increased from 8 to 13 MPa after heat treatment. The HAP heat-treated samples showed higher corrosion resistance (Rp = 65.85 kΩ/cm2; Icorr = 0.63 µA/cm2; Ecorr = −167 mV/ECS) compared to as-deposited and uncoated samples.

Evaluation of Freezing Methods by Low Temperature X-Ray Diffraction

1977 ◽  
Vol 35 ◽  
pp. 330-333
Author(s):  
T. Gulik-Krzywicki ◽  
M.J. Costello
Keyword(s):  
Biological Materials ◽  
Molecular Organization ◽  
X Ray Diffraction ◽  
Glass Capillary ◽  
X Ray ◽  
Rate Dependent ◽  
Before And After ◽  
Freeze Etching ◽  
Diffraction Patterns ◽  
Set Up

Freeze-etching electron microscopy is currently one of the best methods for studying molecular organization of biological materials. Its application, however, is still limited by our imprecise knowledge about the perturbations of the original organization which may occur during quenching and fracturing of the samples and during the replication of fractured surfaces. Although it is well known that the preservation of the molecular organization of biological materials is critically dependent on the rate of freezing of the samples, little information is presently available concerning the nature and the extent of freezing-rate dependent perturbations of the original organizations. In order to obtain this information, we have developed a method based on the comparison of x-ray diffraction patterns of samples before and after freezing, prior to fracturing and replication.Our experimental set-up is shown in Fig. 1. The sample to be quenched is placed on its holder which is then mounted on a small metal holder (O) fixed on a glass capillary (p), whose position is controlled by a micromanipulator.

A New Polyethylene Corrosion Protecting Coating with Ion Selectivity

2011 ◽  
Vol 314-316 ◽  
pp. 273-278
Author(s):  
Yu Hua Dong ◽  
Ke Ren ◽  
Qiong Zhou
Keyword(s):  
Ion Selectivity ◽  
Nano Particles ◽  
Ammonium Bromide ◽  
Linear Low Density Polyethylene ◽  
X Ray Diffraction ◽  
Sulfosalicylic Acid ◽  
X Ray ◽  
Chemically Modified ◽  
Before And After ◽  
Industrial Standards

Linear low density polyethylene (LLDPE) was chemically modified with grafting maleic anhydride (MAH) monomer on its backbone by melting blending. Nano-particles SiO2 was modified by cationic surfactant hexadecyl trimethyl ammonium bromide (CTAB) and anionic surfactant sulfosalicylic acid (SSA) and added to PE coating respectively. Measurement of membrane potential showed that the coating containing modified SiO2 nano-particles had characteristic of ion selectivity. The properties of the different coatings were investigated according to relative industrial standards. Experimental results indicated that PE coating with ion selectivity had better performances, such as adhesion strength, cathodic disbonding and anti-corrosion, than those of coating without ion selectivity. Crystal structure of the coatings before and after alkali corrosion was characterized by Fourier transform infrared spectra (FTIR) and X-ray diffraction (XRD). Structure of the coating without ion selectivity was damaged by NaOH alkali solution, causing mechanical properties being decreased. And the structure of the ion selective coatings was not affected.

scholarly journals Stable and Metastable Phase Equilibria Involving the Cu6Sn5 Intermetallic

2021 ◽  
Author(s):  
A. Leineweber ◽  
M. Löffler ◽  
S. Martin
Keyword(s):  
Phase Equilibria ◽  
Electron Backscatter Diffraction ◽  
Metastable Phase ◽  
Stable Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Ordered Phases ◽  
Backscatter Diffraction ◽  
Kinetics Of

Abstract Cu6Sn5 intermetallic occurs in the form of differently ordered phases η, η′ and η′′. In solder joints, this intermetallic can undergo changes in composition and the state of order without or while interacting with excess Cu and excess Sn in the system, potentially giving rise to detrimental changes in the mechanical properties of the solder. In order to study such processes in fundamental detail and to get more detailed information about the metastable and stable phase equilibria, model alloys consisting of Cu3Sn + Cu6Sn5 as well as Cu6Sn5 + Sn-rich melt were heat treated. Powder x-ray diffraction and scanning electron microscopy supplemented by electron backscatter diffraction were used to investigate the structural and microstructural changes. It was shown that Sn-poor η can increase its Sn content by Cu3Sn precipitation at grain boundaries or by uptake of Sn from the Sn-rich melt. From the kinetics of the former process at 513 K and the grain size of the η phase, we obtained an interdiffusion coefficient in η of (3 ± 1) × 10−16 m2 s−1. Comparison of this value with literature data implies that this value reflects pure volume (inter)diffusion, while Cu6Sn5 growth at low temperature is typically strongly influenced by grain-boundary diffusion. These investigations also confirm that η′′ forming below a composition-dependent transus temperature gradually enriches in Sn content, confirming that Sn-poor η′′ is metastable against decomposition into Cu3Sn and more Sn-rich η or (at lower temperatures) η′. Graphic Abstract

Sedimentary Clays as Geopolymer Precursor

2018 ◽  
Vol 39 ◽  
pp. 97-111
Author(s):  
F. Mostefa ◽  
Nasr Eddine Bouhamou ◽  
H.A. Mesbah ◽  
Salima Aggoun ◽  
D. Mekhatria
Keyword(s):  
Sodium Hydroxide ◽  
Mineralogical Composition ◽  
Cementitious Materials ◽  
Raw Material ◽  
X Ray Diffraction ◽  
Calcination Time ◽  
Calorimetric Analysis ◽  
X Ray ◽  
Before And After ◽  
Mechanical Performances

This work aims to study the feasibility of making a geopolymer cement based on dredged sediments, from the Fergoug dam (Algeria) and to evaluate their construction potential particularly interesting in the field of special cementitious materials. These sediments due to their mineralogical composition as aluminosilicates; are materials that can be used after heat treatment. Sedimentary clays were characterized before and after calcination by X-ray diffraction, ATG / ATD, spectroscopy (FTIR) and XRF analysis. The calcination was carried out on the raw material sieved at 80 μm for a temperature of 750 ° C, for 3.4 and 5 hours. The reactivity of the calcined products was measured using isothermal calorimetric analysis (DSC) on pastes prepared by mixing an alkaline solution of sodium hydroxide (NaOH) 8 M in an amount allowing to have a Na / Al ratio close to 1 (1: 1). Also, cubic mortar samples were prepared with a ratio L / S: 0.8, sealed and cured for 24 hours at 60 ° C and then at room temperature until the day they were submited to mechanical testing. to check the extent of geopolymerization. The results obtained allowed to optimize the calcination time of 5 hours for a better reactivity of these sediments, and a concentration of 8M of sodium hydroxide and more suitable to have the best mechanical performances.

PREPARATION OF ANTIMONY-PLATINUM SURFACE ALLOY ELECTRODE BY ATOM DIFFUSION IN THE SOLID PHASE

2006 ◽  
Vol 20 (25n27) ◽  
pp. 3999-4004
Author(s):  
HIROSHI MATSUI ◽  
KAZUFUMI WATANABE
Keyword(s):  
Diffraction Pattern ◽  
Low Temperatures ◽  
Solid Phase ◽  
Electrochemical Measurement ◽  
X Ray Diffraction ◽  
Platinum Surface ◽  
X Ray ◽  
Atom Diffusion ◽  
Heat Treated ◽  
Titanium Substrates

Antimony-platinum bilayers were prepared on titanium substrates by the two-step electrodeposition in the usual baths, and then surface alloys were formed by the atom diffusion in the solid phase. The simple antimony layer was little influenced by the substrate in both the measurements of X-ray diffraction and the i - E characteristic in a sulfuric acid solution. Regarding the bilayers, the catalytic activity in hydrogen evolution reaction was very sensitive to the presence of platinum, while the hydrogen adsorbability was quite insensitive. An interaction between antimony and platinum was confirmed by the appearance of a new dissolution wave in the electrochemical measurement and the occurrence of a new diffraction in the X-ray diffraction pattern after the heat-treatment of about 400°C. Although the new diffraction disagreed with any of the reported alloys, clear diffraction pattern of PtSb 2 alloy was observed, when the bilayers were heat-treated at about 600°C for one hour. Considering the penetration depth of X-ray, the alloying of antimony and platinum seems to occur also at low temperatures at least at the top surface.

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