Radiation-Modification Impact on the Filled Polytetrafluoroethylene Structure and Mechanical Strength

2017 ◽  
Vol 736 ◽  
pp. 29-34 ◽  
Author(s):  
A.P. Morgunov ◽  
I.V. Revina
Keyword(s):  
Electron Microscopy ◽  
Tensile Strength ◽  
Structural Analysis ◽  
Mechanical Strength ◽  
Supramolecular Structure ◽  
Structural Changes ◽  
Tensile Modulus ◽  
Radiation Energy ◽  
Degree Of Crystallinity ◽  
X Ray

The article studies the structure and properties, regularities of their change with the introduction of various fillers and under the influence of gamma – irradiation (γ-radiation). PCM structure study was performed using electron microscopy with scanning electron microscope BS -350 (TESLA) and with X-ray structural analysis method using X-ray diffractometer DRON-3. Shooting of wide-angle X-ray patters was performed in the range of Bragg angles reflection 2Q=5° - 96°. We selected the following properties to study: tensile strength, static tensile modulus. The findings allowed determining: firstly, we determined that based on electron microscopy the supramolecular structural organization depends on the type and percentage of filler in PTFE matrix. Changes take place from lamellar (pure PTFE) to a defective spherulitic (20% of coke) structure. Secondly, we completed X-ray structural analysis (we determined the degree of crystallinity, crystallite size, with parameters а = b in the hexagonal cell, interlayer distance of amorphous area) showed the nature of supramolecular structure changes according to the nature of the filler and subsequent radiation dose. Thirdly there was conducted connection between changes in mechanical strength (tensile strength, statical module of elasticity) and structural changes; the depth of these changes depends on the original supramolecular structure, type and percentage of the filler and the dose of the absorbed radiation energy. The studies will allow change purposefully the supramolecular structure of polymer composite materials to improve the performance properties.

scholarly journals ANALYSIS OF STRUCTURAL CHANGES OF CELLULOSE COMPONENT IN PROCESS OF ELEMENTARIZATION OF FLAX FIBERS

2017 ◽  
Vol 60 (6) ◽  
pp. 102 ◽  
Author(s):  
Alexandr E. Zavadskii ◽  
Valeria G. Stokozenko ◽  
Andrey P. Moryganov ◽  
Igor Yu. Larin
Keyword(s):  
Supramolecular Structure ◽  
Structural Changes ◽  
Raw Materials ◽  
Diffraction Method ◽  
Degree Of Crystallinity ◽  
X Ray ◽  
Flax Fibers ◽  
Cellulose Iβ ◽  
Deep Purification ◽  
Cellulose Component

The comparative research of composition and supramolecular structure of the flax fibers received by methods of a cottonization and a mechanical elementarization under the influence of the cyclic deforming loadings was conducted. It was shown that under the influence of cyclic loadings removal of a considerable part of impurity with the increase in content of cellulose to 80.1% is reached. At the same time, division of complexes onto elementary filament provides the increase in the total surface of material and, as a result, to availability of fibers to the reagents at the subsequent alkaline boiling. X-ray analysis of flax samples with a method of comparison of the normalized parameters of diffraction by crystalline regions of cellulose allowed to establish that degree of crystallinity of a cellulose component of fibers remains constant even at deep purification of raw materials under the influence of cyclic deformations and subsequent boiling. The research of the oriented fibers by X-ray diffraction method has shown that removal of impurity from flax in the course of an elementarization has only weak influence on the sizes of crystallites of cellulose. The increase in the cross sizes of crystallites by 4 – 6% was observed at deep purification of fibers due to the boiling. This phenomenon can be connected with the decrease in influence of a diffraction maximum from impurity on half-width of the equatorial reflex 200 for cellulose Iβ. It should be noted that the longitudinal sizes of crystallites at the same time do not change. It was suggested on possible influence of decrease in content of impurity on supramolecular structure of an amorphous phase of cellulose and as a result on the observed growth of sorption and mechanical properties of flax fibers at an elementarization by method of cyclic deformation.Forcitation:Zavadskii A.E., Stokozenko V.G., Moryganov A.P., Larin I.Yu. Analysis of structural changes of cellulose component in process of elementarization of flax fibers. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2017. V. 60. N 6. P. 102-108.

Phase Transformations in Ti-7w/oMo-3w/oMe Alloy

1974 ◽  
Vol 32 ◽  
pp. 514-515
Author(s):  
S. Fujishiro
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Transmission Electron Microscopy ◽  
Tensile Strength ◽  
Mechanical Processing ◽  
Ray Method ◽  
X Ray ◽  
Transmission Electron ◽  
Water Quench ◽  
Alpha Beta

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.

X-Ray-Optical Multilayer Structures Studied Using High Resolution Electron Microscopy.

1986 ◽  
Vol 77 ◽  
Author(s):  
Mary Beth Stearns ◽  
Amanda K. Petford-Long ◽  
C.-H. Chang ◽  
D. G. Stearns ◽  
N. M. Ceglio ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Substrate Surface ◽  
High Resolution Electron Microscopy ◽  
Atomic Scale ◽  
Degree Of Crystallinity ◽  
Multilayer Systems ◽  
Layer Width ◽  
X Ray ◽  
Resolution Electron

ABSTRACTThe technique of high resolution electron microscopy has been used to examine the structure of several multilayer systems (MLS) on an atomic scale. Mo/Si multilayers, in use in a number of x-ray optical element applications, and Mo/Si multilayers, of interest because of their magnetic properties, have been imaged in cross-section. Layer thicknesses, flatness and smoothness have been analysed: the layer width can vary by up to 0.6nm from the average value, and the layer flatness depends on the quality of the substrate surface for amorphous MLS, and on the details of the crystalline growth for the crystalline materials. The degree of crystallinity and the crystal orientation within the layers have also been investigated. In both cases, the high-Z layers are predominantly crystalline and the Si layers appear amorphous. Amorphous interfacial regions are visible between the Mo and Si layers, and crystalline cobalt suicide interfacial regions between the Co and Si layers. Using the structural measurements obtained from the HREM results, theoretical x-ray reflectivity behaviour has been calculated. It fits the experimental data very well.

Size dependent behavior of Fe3O4crystals during electrochemical (de)lithiation: an in situ X-ray diffraction, ex situ X-ray absorption spectroscopy, transmission electron microscopy and theoretical investigation

2017 ◽  
Vol 19 (31) ◽  
pp. 20867-20880 ◽  
Author(s):  
David C. Bock ◽  
Christopher J. Pelliccione ◽  
Wei Zhang ◽  
Janis Timoshenko ◽  
K. W. Knehr ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Structural Changes ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
X Ray ◽  
Size Dependent ◽  
Transmission Electron ◽  
Dependent Behavior ◽  
X Ray Absorption

Crystal and atomic structural changes of Fe3O4upon electrochemical (de)lithiation were determined.

scholarly journals Structural Changes of Mo/ZSM-5 Catalysts During the Methane Dehydroaromatization

2009 ◽  
Vol 12 (1) ◽  
pp. 9 ◽  
Author(s):  
Z.R. Ismagilov ◽  
E.V. Matus ◽  
I.Z. Ismagilov ◽  
M.A. Kerzhentsev ◽  
V.I. Zailovskii ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Structural Changes ◽  
Atomic Ratio ◽  
X Ray ◽  
Reducing Atmosphere ◽  
Structure Changes ◽  
Transmission Electron ◽  
Methane Dehydroaromatization ◽  
Naoh Treatment ◽  
Mo Content

<p>The structure changes of Mo/ZSM-5 catalysts with different Mo content (2 and 10 wt. % Mo) and Si/Al atomic ratio (17, 30 and 45) during the methane dehydroaromatization have been investigated by X-ray powder diffractometry, N<sub>2</sub> adsorption and transmission electron microscopy. The treatment of Mo/ZSM-5 catalysts in reducing atmosphere (CH<sub>4</sub> or H<sub>2</sub>) at about 700 °C promotes development of mesoporous system. The pores are open to the exterior of the zeolite grain and have an entrance diameter of ~ 4-10 nm. It is proposed that mesopore formation in Mo/ZSM-5 catalyst is connected with the dealumination of zeolite. The mesopore formation in the parent H-ZSM-5 zeolite by NaOH treatment does not improve the activity of /ZSM-5 catalyst.</p>

A Study of Phase Reactions in a Complex 4.5 Al–3.5 Ti–Ni Base Alloy

1960 ◽  
Vol 4 ◽  
pp. 233-243
Author(s):  
John F. Radavich ◽  
W. J. Boesch
Keyword(s):  
Electron Microscopy ◽  
High Temperature ◽  
Structural Changes ◽  
Base Alloy ◽  
Phase Changes ◽  
X Ray Diffraction ◽  
High Temperature Alloy ◽  
X Ray ◽  
Nickel Base ◽  
Precipitated Phases

AbstractAn investigation of the phase changes in a complex aluminum-titanium-hardened nickel-base high-temperature alloy was carried out after solutioning at high temperatures and aging at lower temperatures. The physical distribution and size of the precipitated phases were studied by electron microscopy. X-ray diffraction and fluorescence analyses were carried out on chemically extracted residues. The results of the xtructure changes as well as correlation of some physical properties with the structural changes are presented.

scholarly journals Characterization of Serpentines from Different Regions by Transmission Electron Microscopy, X-ray Diffraction, BET Specific Surface Area and Vibrational and Electronic Spectroscopy

Fibers ◽  
2019 ◽  
Vol 7 (5) ◽  
pp. 47 ◽  
Author(s):  
Miguel A. Rivero Crespo ◽  
Dolores Pereira Gómez ◽  
María V. Villa García ◽  
José M. Gallardo Amores ◽  
Vicente Sánchez Escribano
Keyword(s):  
Electron Microscopy ◽  
Relative Intensity ◽  
Electronic Spectroscopy ◽  
Visible Region ◽  
Band Gap Energy ◽  
Degree Of Crystallinity ◽  
X Ray Diffraction ◽  
Oh Groups ◽  
X Ray ◽  
Xrd Patterns

Serpentinite powdered samples from four different regions were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), SBET and porosity measurements, UV-Vis and Infrared Spectroscopy of the skeletal region and surface OH groups. SEM micrographs of the samples showed a prismatic morphology when the lizardite was the predominant phase, while if antigorite phase prevailed, the particles had a globular morphology. The few fibrous-shaped particles, only observed by SEM and weakly detected by XRD on MO-9C and MO13 samples, were characteristic of the chrysotile phase. All diffraction XRD patterns showed characteristic peaks of antigorite and lizardite serpentine phases, with crystallite sizes in the range 310–250 Å and with different degrees and types of carbonation processes, one derived from the transformation of the serpentine, generating dolomite, and another by direct precipitation of calcite. The SBET reached values between 38–24 m2∙g−1 for the samples less crystalline, in agreement with the XRD patterns, while those with a higher degree of crystallinity gave values close to 8–9 m2∙g−1. In the UV region all electronic spectra were dominated by the absorption edge due to O2− → Si4+ charge transfer transition, with Si4+ in tetrahedral coordination, corresponding to a band gap energy of ca 4.7 eV. In the visible region, 800–350 nm, the spectra of all samples, except Donai, presented at least two weak and broad absorptions centred in the range 650–800 and 550–360 nm, associated with the presence of Fe3+ ions from the oxidation of structural Fe2+ ions in the serpentinites ((MgxFe2+1−x)3Si2O5(OH)4). The relative intensity of the IR bands corresponding to the stretching modes of the OH’s groups indicated the prevalence of one of the two phases, antigorite or lizardite, in the serpentinites. We proposed that the different relative intensity of these bands could be considered as diagnostic to differentiate the predominance of these phases in serpentinites.

The structural changes of polycrystalline film C60/C70: Ni caused by Ni diffusion

1996 ◽  
Vol 11 (12) ◽  
pp. 3146-3151 ◽  
Author(s):  
E. Czerwosz ◽  
P. Byszewski ◽  
R. Diduszko ◽  
H. Wronka ◽  
P. Dluźewski ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Raman Spectroscopy ◽  
Structural Changes ◽  
Thermal Conditions ◽  
Vacuum Deposition ◽  
X Ray Diffraction ◽  
Polycrystalline Structure ◽  
X Ray ◽  
Transmission Electron

C60/C70: Ni films with 1.5 wt. % Ni concentration obtained by vacuum deposition under different thermal conditions have been investigated. The structural changes of the layers were investigated by transmission electron microscopy, electron and x-ray diffraction, and Raman spectroscopy. The polycrystalline structure was detected for the layers grown at approximately 450 K on the substrate. At elevated temperature and maintained temperature gradient on the substrate during the process, the changes of the layer's structure and the formation of Ni microcrystals were observed. The Ni microcrystals (5–10 nm in the diameter) and the elongated shapes dimensioned 10 × 150 nm were perceived.

scholarly journals Preparation and Characterization of K-Carrageenan/Nanosilica Biocomposite Film

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Lokesh R. Rane ◽  
Niranjan R. Savadekar ◽  
Pravin G. Kadam ◽  
Shashank T. Mhaske
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Contact Angle ◽  
Tensile Strength ◽  
Water Vapour ◽  
Transmission Rate ◽  
Composite Films ◽  
Tensile Modulus ◽  
Water Vapour Transmission Rate ◽  
Scanning Electron

The purpose of this study is to improve the performance properties of K-carrageenan (K-CRG) by utilizing nanosilica (NSI) as the reinforcing agent. The composite films were prepared by solution casting method. NSI was added up to 1.5% in the K-CRG matrix. The prepared films were characterized for mechanical (tensile strength, tensile modulus, and elongation at break), thermal (differential scanning calorimetry, thermogravimetric analysis), barrier (water vapour transmission rate), morphological (scanning electron microscopy), contact angle, and crystallinity properties. Tensile strength, tensile modulus, and crystallinity were found to have increased by 13.8, 15, and 48% whereas water vapour transmission rate was found to have decreased by 48% for 0.5% NSI loaded K-CRG composite films. NSI was found to have formed aggregates for concentrations above 0.5% as confirmed by scanning electron microscopy. Melting temperature, enthalpy of melting, and degradation temperature of K-CRG increased with increase in concentration of NSI in K-CRG. Contact angle also increased with increase in concentration of NSI in K-CRG, indicating the decrease in hydrophilicity of the films improving its water resistance properties. This knowledge of the composite film could make beneficial contributions to the food and pharmaceutical packaging applications.

Study on Microstructure and Property of Diffusion-Bonded Mo-Cu Joints

2012 ◽  
Vol 508 ◽  
pp. 178-182
Author(s):  
Jian Zhang ◽  
Guo Qiang Luo ◽  
Mei Juan Li ◽  
Qiang Shen ◽  
Lian Meng Zhang
Keyword(s):  
Electron Microscopy ◽  
Mechanical Property ◽  
Tensile Strength ◽  
Electron Probe ◽  
Bonding Process ◽  
Interfacial Structure ◽  
X Ray Diffraction ◽  
Strength Measurement ◽  
X Ray ◽  
Scanning Electron

Mo and Cu Were Bonded Successfully by Means of Vacuum Diffusion Bonding. The Interfacial Structure of the Joints Was Studied by Scanning Electron Microscopy (SEM), Electron Probe Microanalysis (EPMA), Energy Dispersive X-Ray Spectrometer (EDS) and X-Ray Diffraction (XRD), the Mechanical Property Is Tested by Tensile Strength Measurement. The Results Showed that the Differentatoms Diffused to each other in the Bonding Process. A Mo-Cu Solid Solution Was Formed in the Joint and with No Intermetallic Compounds. The Tensile Strength of the Joint Increased with the Increasing of Temperature, however, while the Holding Time Increased, the Strength Increased in the First Stages and then Decreases. It Were Observed that the Fracture Mode of the Joints Was a Brittle Fracture.

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