scholarly journals Hydrogen Sorption Behavior of Cast Ag-Mg Alloys

Materials ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 270
Author(s):  
Adam Dębski ◽  
Sylwia Terlicka ◽  
Anna Sypien ◽  
Władysław Gąsior ◽  
Magda Pęska ◽  
...  
Keyword(s):  
Intermetallic Phase ◽  
Magnesium Content ◽  
Decomposition Temperature ◽  
Phase Region ◽  
Mg Alloys ◽  
Hydrogen Sorption ◽  
Sorption Behavior ◽  
Kinetic Properties ◽  
Scanning Calorimetry ◽  
Two Phase

In this paper, the hydrogen sorption properties of casted Ag-Mg alloys were investigated. The obtained alloys were structurally analyzed by X-ray diffraction (XRD) and observed by scanning electron microscopy (SEM). The study was carried out for four alloys from the two-phase region (Mg) + γ′ (AgMg4) with nominal concentrations of 5 wt. %, 10 wt. %, 15 wt. %, and 20 wt. % Ag, four alloys with nominal compositions equivalent to intermetallic phases: AgMg4, AgMg3, AgMg, and Ag3Mg, one alloy from the two-phase region AgMg + Ag3Mg (Ag60Mg40), and one alloy from the two-phase region AgMg + AgMg3 (Ag40Mg60). The hydrogenation process was performed using a Sievert-type sorption analyzer. The hydride decomposition temperature and kinetic properties of the synthesized hydrides were investigated by differential scanning calorimetry (DSC) coupled with thermogravimetric analysis (TGA). Samples with high magnesium content were found to readily absorb significant amounts of hydrogen, while hydrogen absorption was not observed for samples with silver concentrations higher than 50 at. % (AgMg intermetallic phase).

Alloy Effects And Extended Solubilities In Binary Mixtures Of Nanometer-Sized Fe-Cu Crystals

1991 ◽  
Vol 238 ◽  
Author(s):  
J. Eckert ◽  
R. Birringer ◽  
J. C. Holzer ◽  
C. E. Krill ◽  
W. L. Johnson
Keyword(s):  
Binary Mixtures ◽  
Phase Region ◽  
Alloy Formation ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Two Phase ◽  
Transmission Electron ◽  
Thermodynamic Conditions ◽  
20 Nm

ABSTRACTBinary mixtures of Fe-Cu powders in the range of 10–95 at.% Fe have been prepared by mechanical alloying and investigated by x-ray diffraction, differential scanning calorimetry (DSC), and transmission electron microscopy (TEM). The final grain sizes of the powders vary between 6 and 20 nm, and depend on the composition of the material. Indications for the formation of single-phase alloys with up to 60 at.% Fe in Cu and 20 at.% Cu in Fe have been found although the Fe-Cu system exhibits only vanishingly small solid solubilities under equilibrium conditions. Between 60 at.% and 80 at.% Fe a two-phase region of fee and bec solid solutions exists. Alloy formation is discussed with respect to the thermodynamic conditions of the material. The influence of the large grain boundary fraction, as well as the role of internal strains and stored enthalpies introduced by ball milling, is critically assessed.

Differential Scanning Calorimetry and Metallographic Analysis of Fe-Si Electrical Steel

2014 ◽  
Vol 782 ◽  
pp. 129-132
Author(s):  
Martin Sopko ◽  
František Kováč ◽  
Ivan Petryshynets ◽  
Mária Molnárová ◽  
Petra Gavendová
Keyword(s):  
Differential Scanning Calorimetry ◽  
Phase Transformation ◽  
Electrical Steel ◽  
Phase Region ◽  
Metallographic Analysis ◽  
Dsc Analysis ◽  
Scanning Calorimetry ◽  
Two Phase ◽  
Si Content ◽  
Grain Boundary Motion

The microstructure development in cold rolled electrical steel under dynamic heat treatments was subjected to investigation. Significantly distinguish types of microstructures were obtained in the investigated steels confirming the different character of grain boundary motion. Application of annealing temperature within two phase region (austenite+ferrite) leads to abnormal grain growth in silicon steels. Moreover, in the optimum temperature range, there was a particular temperature leading to the most optimal microstructure and texture[1]. The effect of Si content on the phase transition temperature of the electrical steel (0.6, 1, 2.5, 2.9 % Si) was studied by using differential scanning calorimetry (DSC) analysis. The result indicated that DSC analysis could be used to detect the shift temperature of phase transformation in the electrical steel with different Si addition. DSC have been used in thermochemical studies and as complementary to the study of phase transformation. It can be used as a compliment to optical and electron microscopy.

Hydrogen Absorption/Desorption in Nanostructured Fe- and Ti-Doped Mg2Ni Alloys

2010 ◽  
Vol 297-301 ◽  
pp. 745-756
Author(s):  
Isabel C. Atías Adrián ◽  
Fabio A. Deorsola ◽  
G.A. Ortigoza-Villalba ◽  
Bruno DeBenedetti ◽  
Marcello Baricco
Keyword(s):  
Activation Energy ◽  
Hydrogen Storage ◽  
Hydrogen Sorption ◽  
Sorption Behavior ◽  
Slight Reduction ◽  
Scanning Calorimetry ◽  
Temperature Synthesis ◽  
Ni Alloys ◽  
High Temperature Synthesis ◽  
Lower Activation

Nanostructured Mg2Ni, Fe-doped and Ti-doped Mg2Ni alloys for hydrogen storage applications have been produced by means of Mechanically Activated Self-propagating High temperature Synthesis (MASHS). Different molar compositions of Fe and Ti (0.1; 0.3 and 0.5) have been studied in order to determine their influence in the hydrogen sorption properties. Different Mg-Ni based alloys have been tested in order to study their hydrogen sorption behavior. The hydrogenation was carried out in a Pressflow Gas Controller. Subsequently, the dehydrogenation process was conducted by means of a Differential Scanning Calorimetry (DSC) equipped with an H2 detector of the purged gas. The MASHS method has been demonstrated to be effective for the obtainment of nanostructured pure and doped Mg2Ni intermetallics. In addition, the materials produced showed hydrogen storage capacities superior to 4wt%, especially in the case of Fe-doped Mg2Ni and a slight reduction of desorption temperature was reached with Ti-doped Mg2Ni. Finally, the activation energy of the dehydrogenation process was evaluated and Ti-doped sample exhibited the lower activation energy value. Obtained results are promising for technological applications of Mg-based alloys.

Hydrogen Sorption in Magnesium Nanoparticles: Size- and Surface-related Phenomena

2009 ◽  
Vol 1216 ◽  
Author(s):  
Luca Pasquini ◽  
Elsa Callini ◽  
Emanuela Piscopiello ◽  
Amelia Montone ◽  
Torben René Jensen ◽  
...  
Keyword(s):  
Particle Surface ◽  
Intermetallic Phase ◽  
Shell Morphology ◽  
Inert Gas ◽  
Hydrogen Sorption ◽  
Material Structure ◽  
Sorption Behavior ◽  
Gas Condensation ◽  
Inert Gas Condensation ◽  
Dimensional Growth

AbstractThe aim of this work is the investigation of the metal-hydride transformation in magnesium (Mg) nanoparticles both as a function of particle size and in response to surface functionalization by clusters of transition metals (TM): Pd, Ni, Ti.Mg nanoparticles were synthesized by the inert-gas condensation technique, which yields single crystals with six-fold symmetry whose average size can be controlled by tuning the inert gas pressure. After the synthesis the nanoparticles were passivated by slow exposure to oxygen, obtaining a core-shell morphology where a metallic core is coated by a MgO shell of about 5 nm thickness.The material structure was investigated by Transmission Electron Microscopy (TEM), also in High Resolution (HRTEM) mode, and by X-Ray Diffraction (XRD). The sorption kinetics were analysed by a volumetric Sievert apparatus, which also allowed for a determination of the activation energies.Small nanoparticles (≈35 nm) display interesting kinetics with gravimetric capacity of 4.5 wt.% at saturation, limited by the oxide fraction. Hydride formation proceeds by one-dimensional growth controlled by diffusion through the hydride, while the reverse transformation to metal involves interface-controlled three-dimensional growth of nuclei formed at constant rate.On the contrary, large nanoparticles (≈450 nm) exhibit very low reactivity due to reduced probability of hydrogen dissociation/recombination and nucleation at the particle surface. For this reason, large nanoparticles were surface-decorated by TM through in situ evaporation in the inert-gas condensation chamber. This procedure results in clusters of 3-4 nm located over a portion of the MgO shell, as shown by XRD and HRTEM on Pd-decorated sample. This treatment results in dramatically improved hydrogen sorption behavior. In fact, previously inert nanoparticles now exhibit of up to 5.6 wt.%.Real-time diffraction studies using Synchrotron Radiation were carried out during hydrogen desorption on the Pd-decorated nanoparticles. We clearly show that a Mg-Pd intermetallic phase is formed after the first heating treatment and takes active part in the transformation.

Solution Properties and Phase Behavior of Ammonium Hexylene Octyl Succinate in Water and Water-Oil System

1970 ◽  
Vol 3 (1) ◽  
Author(s):  
Md. Hamidul Kabir ◽  
Ravshan Makhkamov ◽  
Shaila Kabir
Keyword(s):  
Critical Micelle Concentration ◽  
Phase Behavior ◽  
Liquid Crystalline ◽  
Carbon Number ◽  
Phase Region ◽  
Solution Properties ◽  
Middle Phase ◽  
Two Phase ◽  
Lamellar Liquid Crystal ◽  
Drug Ingredient

The solution properties and phase behavior of ammonium hexylene octyl succinate (HOS) was investigated in water and water-oil system. The critical micelle concentration (CMC) of HOS is lower than that of anionic surfactants having same carbon number in the lipophilic part. The phase diagrams of a water/ HOS system and water/ HOS/ C10EO8/ dodecane system were also constructed. Above critical micelle concentration, the surfactant forms a normal micellar solution (Wm) at a low surfactant concentration whereas a lamellar liquid crystalline phase (La) dominates over a wide region through the formation of a two-phase region (La+W) in the binary system. The lamellar phase is arranged in the form of a biocompatible vesicle which is very significant for the drug delivery system. The surfactant tends to be hydrophilic when it is mixed with C10EO8 and a middle-phase microemulsion (D) is appeared in the water-surfactant-dodecane system where both the water and oil soluble drug ingredient can be incorporated in the form of a dispersion. Hence, mixing can tune the hydrophile-lipophile properties of the surfactant. Key words: Ammonium hexylene octyl succinate, mixed surfactant, lamellar liquid crystal, middle-phase microemulsion. Dhaka Univ. J. Pharm. Sci. Vol.3(1-2) 2004 The full text is of this article is available at the Dhaka Univ. J. Pharm. Sci. website

scholarly journals Effect of Nanofiller Content on Dynamic Mechanical and Thermal Properties of Multi-Walled Carbon Nanotube and Montmorillonite Nanoclay Filler Hybrid Shape Memory Epoxy Composites

Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 700
Author(s):  
Muhamad Hasfanizam Mat Yazik ◽  
Mohamed Thariq Hameed Sultan ◽  
Mohammad Jawaid ◽  
Abd Rahim Abu Talib ◽  
Norkhairunnisa Mazlan ◽  
...  
Keyword(s):  
Shape Memory ◽  
High Performance ◽  
Loss Modulus ◽  
Decomposition Temperature ◽  
Hybrid Nanocomposites ◽  
Mechanical And Thermal Properties ◽  
Scanning Calorimetry ◽  
Hybrid Filler ◽  
Dynamic Mechanical ◽  
Tan Δ

The aim of the present study has been to evaluate the effect of hybridization of montmorillonite (MMT) and multi-walled carbon nanotubes (MWCNT) on the thermal and viscoelastic properties of shape memory epoxy polymer (SMEP) nanocomposites. In this study, ultra-sonication was utilized to disperse 1%, 3%, and 5% MMT in combination with 0.5%, 1%, and 1.5% MWCNT into the epoxy system. The fabricated SMEP hybrid nanocomposites were characterized via differential scanning calorimetry, dynamic mechanical analysis, and thermogravimetric analysis. The storage modulus (E’), loss modulus (E”), tan δ, decomposition temperature, and decomposition rate, varied upon the addition of the fillers. Tan δ indicated a reduction of glass transition temperature (Tg) for all the hybrid SMEP nanocomposites. 3% MMT/1% MWCNT displayed best overall performance compared to other hybrid filler concentrations and indicated a better mechanical property compared to neat SMEP. These findings open a way to develop novel high-performance composites for various potential applications, such as morphing structures and actuators, as well as biomedical devices.

scholarly journals Revisiting the Bøggild Intergrowth in Iridescent Labradorite Feldspars: Ordering, Kinetics, and Phase Equilibria

Minerals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 727
Author(s):  
Shiyun Jin ◽  
Huifang Xu ◽  
Seungyeol Lee
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Atom Probe ◽  
Phase Region ◽  
Two Phase ◽  
Subsolidus Phase ◽  
Plagioclase Feldspar ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Transmission

The enigmatic Bøggild intergrowth in iridescent labradorite crystals was revisited in light of recent work on the incommensurately modulated structures in the intermediated plagioclase. Five igneous samples and one metamorphic labradorite sample with various compositions and lamellar thicknesses were studied in this paper. The lamellar textures were characterized with conventional transmission electron microscopy (TEM) and scanning transmission electron microscopy (STEM). The compositions of individual lamellae were analyzed with high-resolution energy-dispersive X-ray spectroscopy (EDS) mapping and atom probe tomography (APT). The average structure states of the studied samples were also compared with single-crystal X-ray diffraction data (SC-XRD). The Na-rich lamellae have a composition of An44–48, and the Ca-rich lamellae range from An56 to An63. Significant differences between the lamellar compositions of different samples were observed. The compositions of the Bøggild intergrowth do not only depend on the bulk compositions, but also on the thermal history of the host rock. The implications on the subsolidus phase relationships of the plagioclase feldspar solid solution are discussed. The results cannot be explained by a regular symmetrical solvus such as the Bøggild gap, but they support an inclined two-phase region that closes at low temperature.

scholarly journals A Characteristic Study of Polylactic Acid/Organic Modified Montmorillonite (PLA/OMMT) Nanocomposite Materials after Hydrolyzing

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 376
Author(s):  
Su-Mei Huang ◽  
Jiunn-Jer Hwang ◽  
Hsin-Jiant Liu ◽  
An-Miao Zheng
Keyword(s):  
Thermal Stability ◽  
Polylactic Acid ◽  
Decomposition Temperature ◽  
Material Strength ◽  
Scanning Calorimetry ◽  
Hydrolysis Process ◽  
Twin Screw ◽  
Thermal Pressing ◽  
Organophilic Clay ◽  
Mmt Clay

In this study, the montmorillonite (MMT) clay was modified with NH4Cl, and then the structures were exfoliated or intercalated in a polylactic acid (PLA) matrix by a torque rheometer in the ratio of 0.5, 3.0, 5.0 and 8.0 wt%. X-ray diffraction (XRD) revealed that the organic modified-MMT(OMMT) was distributed successfully in the PLA matrix. After thermal pressing, the thermal stability of the mixed composites was measured by a TGA. The mixed composites were also blended with OMMT by a co-rotating twin screw extruder palletizing system, and then injected for the ASTM-D638 standard specimen by an injection machine for measuring the material strength by MTS. The experimental results showed that the mixture of organophilic clay and PLA would enhance the thermal stability. In the PLA mixed with 3 wt% OMMT nanocomposite, the TGA maximum decomposition temperature (Tmax) rose from 336.84 °C to 339.08 °C. In the PLA mixed with 5 wt% OMMT nanocomposite, the loss of temperature rose from 325.14 °C to 326.48 °C. In addition, the elongation rate increased from 4.46% to 10.19% with the maximum loading of 58 MPa. After the vibrating hydrolysis process, the PLA/OMMT nanocomposite was degraded through the measurement of differential scanning calorimetry (DSC) and its Tg, Tc, and Tm1 declined.

scholarly journals Synthesis and Characterization of N-Substituted Polyether-Block-Amide Copolymers

Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 773
Author(s):  
Jyun-Yan Ye ◽  
Kuo-Fu Peng ◽  
Yu-Ning Zhang ◽  
Szu-Yuan Huang ◽  
Mong Liang
Keyword(s):  
Titanium Isopropoxide ◽  
Decomposition Temperature ◽  
Phenyl Isocyanate ◽  
Cross Linking ◽  
Resonance Spectroscopy ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Degradation Temperature ◽  
Melt Polycondensation ◽  
Structural Regularity

A series of N-substituted polyether-block-amide (PEBA-X%) copolymers were prepared by melt polycondensation of nylon-6 prepolymer and polytetramethylene ether glycol at an elevated temperature using titanium isopropoxide as a catalyst. The structure, thermal properties, and crystallinity of PEBA-X% were investigated using nuclear magnetic resonance spectroscopy, Fourier-transform infrared spectroscopy, differential scanning calorimetry, wide angle X-ray diffraction, and thermogravimetric analysis. In general, the crystallinity, melting point, and thermal degradation temperature of PEBA-X% decreased as the incorporation of N-methyl functionalized groups increased, owing to the disruption caused to the structural regularity of the copolymer. However, in N-acetyl functionalized analogues, the crystallinity first dropped and then increased because of a new γ form arrangement that developed in the microstructure. After the cross-linking reaction of the N-methyl-substituted derivative, which has electron-donating characteristics, with poly(4,4′-methylenebis(phenyl isocyanate), the decomposition temperature of the resulting polymer significantly increased, whereas no such improvements could be observed in the case of the electro-withdrawing N-acetyl-substituted derivative, because of the incompleteness of its cross-linking reaction.

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