scholarly journals Ethylene-Octene Copolymers/Organoclay Nanocomposites: Preparation and Properties

2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
Alice Tesarikova ◽  
Dagmar Merinska ◽  
Jiri Kalous ◽  
Petr Svoboda
Keyword(s):  
Barrier Properties ◽  
Mechanical Analysis ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Uv Aging ◽  
Dynamical Mechanical Analysis ◽  
Elongation At Break ◽  
X Ray ◽  
Transmission Electron ◽  
Nucleation Agents

Two ethylene-octene copolymers with 17 and 45 wt.% of octene (EOC-17 and EOC-45) were compared in nanocomposites with Cloisite 93A. EOC-45 nanocomposites have a higher elongation at break. Dynamical mechanical analysis (DMA) showed a decrease oftan⁡δwith frequency for EOC-17 nanocomposites, but decrease is followed by an increase for EOC-45 nanocomposites; DMA showed also increased modulus for all nanocomposites compared to pure copolymers over a wide temperature range. Barrier properties were improved about 100% by addition of organoclay; they were better for EOC-17 nanocomposites due to higher crystallinity. X-ray diffraction (XRD) together with transmission electron microscopy (TEM) showed some intercalation for EOC-17 but much better dispersion for EOC-45 nanocomposites. Differential scanning calorimetry (DSC) showed increased crystallization temperatureTcfor EOC-17 nanocomposite (aggregates acted as nucleation agents) but decreaseTcfor EOC-45 nanocomposite together with greatly influenced melting peak. Accelerated UV aging showed smaller C=O peak for EOC-45 nanocomposites.

scholarly journals Effects of Sintering Temperature on Densification, Microstructure and Mechanical Properties of Al-Based Alloy by High-Velocity Compaction

Metals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 218
Author(s):  
Xianjie Yuan ◽  
Xuanhui Qu ◽  
Haiqing Yin ◽  
Zaiqiang Feng ◽  
Mingqi Tang ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
High Velocity ◽  
Sintered Density ◽  
Sintering Temperature ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
High Velocity Compaction ◽  
Sintered Temperature

This present work investigates the effects of sintering temperature on densification, mechanical properties and microstructure of Al-based alloy pressed by high-velocity compaction. The green samples were heated under the flow of high pure (99.99 wt%) N2. The heating rate was 4 °C/min before 315 °C. For reducing the residual stress, the samples were isothermally held for one h. Then, the specimens were respectively heated at the rate of 10 °C/min to the temperature between 540 °C and 700 °C, held for one h, and then furnace-cooled to the room temperature. Results indicate that when the sintered temperature was 640 °C, both the sintered density and mechanical properties was optimum. Differential Scanning Calorimetry, X-ray diffraction of sintered samples, Scanning Electron Microscopy, Energy Dispersive Spectroscopy, and Transmission Electron Microscope were used to analyse the microstructure and phases.

Characterization of the Phase Transformations in the Shape Memory Alloy Ni-36 at.% Al

1991 ◽  
Vol 246 ◽  
Author(s):  
J.A. Horton ◽  
E.P. George ◽  
C.J. Sparks ◽  
M.Y. Kao ◽  
O.B. Cavin ◽  
...  
Keyword(s):  
High Temperature ◽  
Shape Memory ◽  
Phase Transformations ◽  
Hot Extrusion ◽  
Exothermic Peak ◽  
Nickel Aluminum ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron

AbstractA survey by differential scanning calorimetry (DSC) and recovery during heating of indentations on a series of nickel-aluminum alloys showed that the Ni-36 at.% Al composition has the best potential for a recoverable shape memory effect at temperatures above 100°C. The phase transformations were studied by high temperature transmission electron microscopy (TEM) and by high temperature x-ray diffraction (HTXRD). Quenching from 1200°C resulted in a single phase, fully martensitic structure. The initial quenched-in martensites were found by both TEM and X-ray diffraction to consist of primarily a body centered tetragonal (bct) phase with some body centered orthorhombic (bco) phase present. On the first heating cycle, DSC showed an endothermic peak at 121°C and an exothermic peak at 289°C, and upon cooling a martensite exothermic peak at 115° C. Upon subsequent cycles the 289°C peak disappeared. High temperature X-ray diffraction, with a heating rate of 2°C/min, showed the expected transformation of bct phase to B2 between 100 and 200°C, however the bco phase remained intact. At 400 to 450°C the B2 phase transformed to Ni2Al and Ni5Al3. During TEM heating experiments a dislocation-free martensite transformed reversibly to B2 at temperatures less than 150°C. At higher temperatures (nearly 600°C) 1/3, 1/3, 1/3 reflections from an ω-like phase formed. Upon cooling, the 1/3, 1/3, 1/3 reflections disappeared and a more complicated martensite resulted. Boron additions suppressed intergranular fracture and, as expected, resulted in no ductility improvements. Boron additions and/or hot extrusion encouraged the formation of a superordered bct structure with 1/2, 1/2, 0 reflections.

scholarly journals Ellagic Acid May Improve Mechanical and Barrier Properties in Films of Starch-A Review Paper

2016 ◽  
Vol 5 (3) ◽  
pp. 61
Author(s):  
J. M. Tirado-Gallegos ◽  
D. R. Sepúlveda-Ahumada ◽  
P. B. Zamudio-Flores ◽  
M. L. Rodríguez-Marin ◽  
Francisco Hernández-Centeno ◽  
...  
Keyword(s):  
Ellagic Acid ◽  
Structural Changes ◽  
Antioxidant Properties ◽  
Barrier Properties ◽  
Packaging Materials ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Film Forming ◽  
Starch Films

<p>Packaging increases the shelf life of food and facilitates its handling, transportation and marketing. The main packaging materials are plastics derived from petroleum, but their accumulation has given rise to environmental problems. An alternative is the use of biodegradable materials. In this regard, starch is an excellent choice because it is an abundant and renewable source with film-forming properties. However, the films obtained from starch have some limitations with respect to their mechanical and barrier properties. Several strategies have been developed in order to improve these limitations, ranging from the addition of lipids to the modification of the polymer structure. The aim of this review was propose the use of ellagic acid as a cross-linking agent that may improves the mechanical and barrier properties in films based on exists reports that phenolic compounds interact with starch-based materials decreasing their rate of retrogradation. Furthermore, ellagic acid is a powerful natural antioxidant, which would allow the production of active packaging with antioxidant properties, in addition to the improvement of the mechanical and barrier properties of starch films. In this concern more studies such as Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry and thermogravimetric analysis are necessary to verify the structural changes and interactions between starch and ellagic acid. We expect extensive use of it in the future of packaging materials.</p>

Preparation and Property of Al87Ce3Ni8.5Mn1.5 Nanophase Amorphous Composites

2011 ◽  
Vol 412 ◽  
pp. 263-266
Author(s):  
Hong Wei Zhang ◽  
Li Li Zhang ◽  
Feng Rui Zhai ◽  
Jia Jin Tian ◽  
Can Bang Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
Volume Fraction ◽  
Material Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures

The higher mechanical strength of Al87Ce3Ni8.5Mn1.5 nanophase amorphous composites has been obtained with two methods. The first nanophase amorphous composites are directly produced by the single roller spin quenching technology. The method taken for the second nanophase amorphous composites is at first to obtain amorphous single-phase alloy, followed by annealed at different temperatures .The formative condition, the microstructure, the particle size, the volume fraction of α-Al phase and microhardness of nanophase amorphous composites etc have been investigated and compared by X-ray diffraction (XRD) and transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The microstructure of composites produced by the second method is higher than the former, the fabricated material structure of the system is more uniform and the process is easier to control.

Millable Polyurethane/Organoclay Nanocomposites: Preparation, Characterization, and Properties

2007 ◽  
Vol 7 (2) ◽  
pp. 634-640 ◽  
Author(s):  
M. Siliani ◽  
M. A. López-Manchado ◽  
J. L. Valentín ◽  
M. Arroyo ◽  
A. Marcos ◽  
...  
Keyword(s):  
Barrier Properties ◽  
Substantial Improvement ◽  
Nanometer Scale ◽  
X Ray Diffraction ◽  
Transformation Techniques ◽  
Covalent Bonds ◽  
X Ray ◽  
Transmission Electron ◽  
Organically Modified ◽  
Diffraction Patterns

Novel millable polyurethane (PU)/organoclay nanocomposites have been successfully prepared by conventional transformation techniques. One natural (C6A) and two organically modified (C15A and C30B) montmorillonites have been used as clays for preparing PU nanocomposites. The optimum dispersion of nanofiller at a nanometer scale in PU matrix was confirmed by X-ray diffraction patterns and transmission electron microscopy. A substantial improvement of the PU properties by addition of only a small amount of organoclay was observed. It is worthy to note that the organoclays show a different interfacial interaction with the PU matrix, which was reflected in different macroscopic properties. Thus, C30B organoclay seems to react with PU chains to form covalent bonds, while C15Aonly interacts physically with PU chains. Mechanical and barrier properties are analyzed.

Crystallization of Amorphous Si In Al/Si Multilayers

1991 ◽  
Vol 230 ◽  
Author(s):  
Toyohiko J. Konno ◽  
Robert Sinclair
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Layered Structure ◽  
Heat Of Reaction ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Amorphous Si

AbstractThe crystallization of amorphous Si in a Al/Si multilayer (with a modulation length of about 120Å) was investigated using transmission electron microscopy, differential scanning calorimetry and X-ray diffraction. Amorphous Si was found to crystallize at about 175 °C with the heat of reaction of 11±2(kJ/mol). Al grains grow prior to the nucleation of crystalline Si. The crystalline Si was found to nucleate within the grown Al layers. The incipient crystalline Si initially grows within the Al layer and then spreads through the amorphous Si and other Al layers. Because of extensive intermixing, the original layered structure is destroyed. The Al(111) texture is also enhanced.

Hardness evolution of Al–Cr–N coatings under thermal load

2008 ◽  
Vol 23 (11) ◽  
pp. 2880-2885 ◽  
Author(s):  
Herbert Willmann ◽  
Paul H. Mayrhofer ◽  
Lars Hultman ◽  
Christian Mitterer
Keyword(s):  
Thermal Load ◽  
Structural Changes ◽  
Single Phase ◽  
Volume Fraction ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Al Content ◽  
Annealing Temperatures ◽  
Transmission Electron

Microstructure and hardness evolution of arc-evaporated single-phase cubic Al0.56Cr0.44N and Al0.68Cr0.32N coatings have been investigated after thermal treatment in Ar atmosphere. Based on a combination of differential scanning calorimetry and x-ray diffraction studies, we can conclude that Al0.56Cr0.44N undergoes only small structural changes without any decomposition for annealing temperatures Ta ⩽ 900 °C. Consequently, the hardness decreases only marginally from the as-deposited value of 30.0 ± 1.1 GPa to 29.4 ± 0.9 GPa with Ta increasing to 900 °C, respectively. The film with higher Al content (Al0.68Cr0.32N) exhibits formation of hexagonal (h) AlN at Ta ⩾ 700 °C, which occurs preferably at grain boundaries as identified by analytical transmission electron microscopy. Hence, the hardness increases from the as-deposited value of 30.1 ± 1.3 GPa to 31.6 ± 1.4 GPa with Ta = 725 °C. At higher temperatures, where the size and volume fraction of the h-AlN phase increases, the hardness decreases to 27.5 ± 1.0 GPa with Ta = 900 °C.

Study on the Preparation and Properties of EVA-G-PU/OMMT Nanocomposites

2010 ◽  
Vol 123-125 ◽  
pp. 247-250
Author(s):  
Yu Qing Zhang ◽  
Yu Xin He ◽  
Li Zhang ◽  
Jun Xian Li
Keyword(s):  
Electron Microscopy ◽  
Mechanical Analysis ◽  
Clay Nanocomposites ◽  
Gravimetric Analysis ◽  
Thermal Gravimetric ◽  
X Ray Diffraction ◽  
Thermal Stabilities ◽  
X Ray ◽  
Transmission Electron ◽  
New Type

A new type of EVA-g-PU/OMMT nanocomposites was synthesized through the method of chemical modification and melt intercalation. FTIR testing showed that the PU prepolymer was grafted on EVA main chains successfully. The structures of EVA-g-PU/OMMT nanocomposites were characterized by X-ray diffraction (XRD) and by high-resolution transmission electron microscopy (HRTEM). The enhanced storage modulus of EVA-g-PU/OMMT nanocomposites was characterized by dynamic mechanical analysis (DMA). The thermal stabilities of EVA/clay nanocomposites were also studied by thermal gravimetric analysis (TGA). Mechanical testing showed that the tensile strength and tear strength of EVA-g-PU/OMMT nanocomposites were far superior to pure EVA.

Characterization of Nanocrystalline γ–Fe2O3Prepared by Wet Chemical Method

1999 ◽  
Vol 14 (4) ◽  
pp. 1570-1575 ◽  
Author(s):  
G. Ennas ◽  
G. Marongiu ◽  
A. Musinu ◽  
A. Falqui ◽  
P. Ballirano ◽  
...  
Keyword(s):  
Isothermal Treatment ◽  
X Ray Diffraction ◽  
Ferrous Chloride ◽  
Scanning Calorimetry ◽  
Direct Transformation ◽  
X Ray ◽  
Transmission Electron ◽  
Xrd Techniques ◽  
Kinetics Of

Homogeneous maghemite (γ–Fe2O3) nanoparticles with an average crystal size around 5 nm were synthesized by successive hydrolysis, oxidation, and dehydration of tetrapyridino-ferrous chloride. Morphological, thermal, and structural properties were investigated by transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and x-ray diffraction (XRD) techniques. Rietveld refinement indicated a cubic cell. The superstructure reflections, related to the ordering of cation lattice vacancies, were not detected in the diffraction pattern. Kinetics of the solid-state phase transition of nanocrystalline maghemite to hematite (α–Fe2O3), investigated by energy dispersive x-ray diffraction (EDXRD), indicates that direct transformation from nanocrystalline maghemite to microcrystalline hematite takes place during isothermal treatment at 385 °C. This temperature is lower than that observed both for microcrystalline maghemite and for nanocrystalline maghemite supported on silica.

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