Co-Deposition of Al–Ni Alloy in NiCl2-AlCl3-1-ethyl-3-methylimidazolium Bromide ([EMIM]Br) Ionic Liquid

2011 ◽  
Vol 121-126 ◽  
pp. 65-69
Author(s):  
Li Peng Zhang ◽  
Xian Jin Yu ◽  
Zhi Wei Ge ◽  
Yun Hui Dong ◽  
Dang Gang Li
Keyword(s):  
Electron Microscopy ◽  
Ionic Liquid ◽  
Room Temperature ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ni Alloys ◽  
Ni Alloy ◽  
Rapidly Solidified ◽  
Scanning Electron

Al-Ni Alloys were obtained from NiCl2-AlCl3-1-ethyl-3-methylimidazolium bromide ([EMIM]Br) ionic liquid at room temperature. The analysis of Al-Ni alloys that co-deposited at different potentials for 2h were performed using Scanning Electron Microscopy (SEM) and X-ray diffraction analysis (XRD). It appears that Ni has been rapidly solidified in the alloys and homogeneous Al-Ni alloys can be obtained at room temperature. As increasing the overpotential, the amount of Ni in the alloys was decreased whereas the amount of Al was increased. The chloride pitting potentials of alloys with the molar ratio of NiCl2/AlCl3/[EMIM]Br 0.03:2:1 was approximately 0.3 V more than pure Al.

scholarly journals Microstructures of Three In-Situ Reinforcements and the Effect on the Tensile Strengths of an Al-Si-Cu-Mg-Ni Alloy

2018 ◽  
Vol 8 (9) ◽  
pp. 1523 ◽  
Author(s):  
Lusha Tian ◽  
Yongchun Guo ◽  
Jianping Li ◽  
Feng Xia ◽  
Minxian Liang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
Simultaneous Formation ◽  
X Ray ◽  
Transmission Electron ◽  
Ni Alloy ◽  
Al3ti Phase ◽  
Scanning Electron

In the present paper, the microstructures of three kinds of in-situ reinforcements Al-Ti-C, Al-Ti-B, and Al-Ti-B-C-Ce were deeply investigated using a combination of scanning electron microscopy, X-ray diffraction spectroscopy, and transmission electron microscopy. The effect of in-situ reinforcements on the room temperature and elevated temperature (350 °C) tensile strengths of Al-13Si-4Cu-1Mg-2Ni alloy were analyzed. It is found that doping with trace amounts of B and Ce, the size of the Al3Ti phase in the in-situ reinforced alloy changed from 80 µm (un-reinforced) to about 10 µm, with the simultaneous formation of the AlTiCe phase. The Al-Ti-B-C-Ce reinforcement which is rapid solidified, was more effective and superior to enhance the tensile strengths of the Al-13Si-4Cu-1Mg-2Ni alloy, both at room and high temperatures than those of addition other reinforcements. The room temperature (RT) strength increased by 19.0%, and the 350 °C-strength increased by 18.4%.

ROOM TEMPERATURE PHOTOLUMINESCENCE OF POLYCRYSTALLINE SIC PREPARED FROM CARBON-SATURATED SI MELT

2002 ◽  
Vol 16 (06n07) ◽  
pp. 1047-1051
Author(s):  
JIANPING MA ◽  
ZHIMING CHEN ◽  
GANG LU ◽  
MINGBIN YU ◽  
LIANMAO HANG ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Uv Light ◽  
X Ray Diffraction ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Composition And Structure ◽  
Light Excitation ◽  
Scanning Electron

Intense photoluminescence (PL) has been observed at room temperature from the polycrystalline SiC samples prepared from carbon-saturated Si melt at a temperature ranging from 1500 to 1650°C. Composition and structure of the samples have been confirmed by means of X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. PL measurements with 325 nm UV light excitation revealed that the room temperature PL spectrum of the samples consists of 3 luminescent bands, the peak energies of which are 2.38 eV, 2.77 eV and 3.06 eV, respectively. The 2.38 eV band is much stronger than the others. It is suggested that some extrinsic PL mechanisms associated with defect or interface states would be responsible to the intensive PL observed at room temperature.

Application of vermiculite and limestone to desulphurization and to the removal of dust during briquette combustion

2003 ◽  
Vol 67 (6) ◽  
pp. 1243-1251 ◽  
Author(s):  
A. Lu ◽  
D. Zhao ◽  
J. Li ◽  
C. Wang ◽  
S. Qin
Keyword(s):  
Electron Microscopy ◽  
Coal Combustion ◽  
Combustion Temperature ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Retention Ratio ◽  
X Ray ◽  
Major Factors ◽  
Chemical Reactant ◽  
Scanning Electron

AbstractSmall domestic cooking furnaces are widely used in China. These cooking furnaces release SO2 gas and dust into the atmosphere and cause serious air pollution. Experiments were conducted to investigate the effects of vermiculite, limestone or CaCO3, and combustion temperature and time on desulphurization and dust removal during briquette combustion in small domestic cooking furnaces. Additives used in the coal are vermiculite, CaCO3 and bentonite. Vermiculite is used for its expansion property to improve the contact between CaCO3 and SO2 and to convey O2 into the interior of briquette; CaCO3 is used as a chemical reactant to react with SO2 to form CaSO4; and bentonite is used to develop briquette strength. Expansion of vermiculite develops loose interior structures, such as pores or cracks, inside the briquette, and thus brings enough oxygen for combustion and sulphation reaction. Effective combustion of the original carbon reduces amounts of dust in the fly ash. X-ray diffraction, optical microscopy, and scanning electron microscopy with energy dispersive X-ray analysis show that S exists in the ash only as anhydrite CaSO4, a product of SO2 reacting with CaCO3 and O2. The formation of CaSO4 effectively reduces or eliminates SO2 emission from coal combustion. The major factors controlling S retention are vermiculite, CaCO3 and combustion temperature. The S retention ratio increases with increasing vermiculite amount at 950°C. The S retention ratio also increases with increasing Ca/S molar ratio, and the best Ca/S ratio is 2-3 for most combustion. With 12 g of the original coal, 1 to 2 g of vermiculite, a molar Ca/S ratio of 2.55 by adding CaCO3, and some bentonite, a S retention ratio >65% can be readily achieved. The highest S retention ratio of 97.9% is achieved at 950°C with addition of 2 g of vermiculite, a Ca/S ratio of 2.55 and bentonite.

Influence of Silicon Nitride on Properties of Corundum Based Castable

2013 ◽  
Vol 634-638 ◽  
pp. 2358-2361
Author(s):  
Jun Cong Wei ◽  
Li Rong Yang
Keyword(s):  
Electron Microscopy ◽  
Thermal Shock ◽  
Thermal Shock Resistance ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
Cold Strength ◽  
X Ray ◽  
Refractory Castables ◽  
Shock Resistance ◽  
Scanning Electron

The effects of Si3N4 addition on the room temperature physical properties and thermal shock resistance properties of corundum based refractory castables were investigated using brown corundum, white corundum and alumina micropowder as the starting materials and pure calcium aluminate as a binder. The phase composition, microstructure, mechanical properties of corundum based castables were investigated by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed that as the increase in Si3N4 addition, the bulk density decreased and apparent porosity increased, the cold strength deduced. However, the residual strength rate increased. That is, the thermal shock resistance was improved. This is because even though the introduction of Si3N4 inhibited the sintering of material and deduced the compactness, microcracks were produced in the materials due to a difference in thermal expansion coefficient. So the thermal shock resistance of corundum based castable was improved.

Synthesis of Nickel Hydroxide with Different Morphologies Using an Ionic Liquid

2010 ◽  
Vol 663-665 ◽  
pp. 1163-1166
Author(s):  
Cun Ying Xu ◽  
Yi Xin Hua
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Ionic Liquid ◽  
Volume Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Reaction Media ◽  
Solvothermal Conditions ◽  
Facile Route ◽  
Scanning Electron

A new and facile route has been developed to synthesize β-Ni(OH)2 nanostructures using ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([Bmim]BF4) as reaction media under solvothermal conditions. The β-Ni(OH)2 with different morphologies, such as nanoflakes, nanoplatelet and nanorods, can be obtained by controlling the volume ratio of the ionic liquid to water and reaction temperature. The as-prepared products were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM).

N-type Ba0.2Co4Sb11.5Te0.5: Optimization of thermoelectric properties by different pressures

2019 ◽  
Vol 33 (03) ◽  
pp. 1950027 ◽  
Author(s):  
Jiaxiang Chen ◽  
Xiaopeng Jia ◽  
Yuewen Zhang ◽  
Haiqiang Liu ◽  
Baomin Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Seebeck Coefficient ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
Absolute Value ◽  
X Ray ◽  
Coefficient Increase ◽  
Maximum Power Factor ◽  
Scanning Electron

The polycrystalline skutterudite [Formula: see text] were successfully synthesized from 1.5 GPa to 3.5 GPa by the high pressure and high temperature (HPHT) method. Negative Seebeck coefficient confirmed the n-type conductivity of all samples. The phase compositions of samples were investigated by X-ray diffraction (XRD) and the microstructures were observed by scanning electron microscopy (SEM). It was found that the grains appeared smaller and the grain boundaries became more abundant when pressures were higher. We measured the electrical properties from room temperature to 723 K. Both the electrical resistivity and absolute value of Seebeck coefficient increase with the increasing synthetic pressure. At 723 K, the maximum power factor of [Formula: see text] was obtained for the sample synthesized under 3 GPa. The maximum ZT value of 0.61 was reached by [Formula: see text] synthesized under 3 GPa and measured at 723 K.

Synthesis of Precipitate Calcium Carbonate with Variation Morphology from Limestone by Using Solution Mixing Method

2019 ◽  
Vol 966 ◽  
pp. 200-203
Author(s):  
Zaenal Arifin ◽  
Triwikantoro ◽  
Bintoro Anang Subagyo ◽  
Mochamad Zainuri ◽  
Darminto
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Calcium Carbonate ◽  
Molar Ratio ◽  
Mixing Process ◽  
X Ray Diffraction ◽  
Precipitate Calcium Carbonate ◽  
X Ray ◽  
Mixing Method ◽  
Scanning Electron

Abstract. In this study, the CaCO3 powder has been successfully synthesized by mixing CaCl2 from natural limestone and Na2CO3 in the same molar ratio. The mixing process of solutions was carried out by employing the molar contents of 0.125, 0.25, 0.375 and 0.5M at varying temperatures of 30, 40, 60 and 80ᴼC. The produced CaCO3 microparticles were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The highest content of aragonite phase with morphology rod-like of the samples is around 29 wt%, resulting from the process using solution of 0.125 M at 80 ᴼC. While at 30 ᴼC and 40 ᴼC produced 100 wt% calcite phase.

scholarly journals Properties of Nanostructure Bismuth Telluride Thin Films Using Thermal Evaporation

2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Swati Arora ◽  
Vivek Jaimini ◽  
Subodh Srivastava ◽  
Y. K. Vijay
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Bismuth Telluride ◽  
Room Temperature ◽  
Thermal Evaporation ◽  
Silicon Substrates ◽  
X Ray Diffraction ◽  
Thermal Evaporation Method ◽  
X Ray ◽  
Scanning Electron

Bismuth telluride has high thermoelectric performance at room temperature; in present work, various nanostructure thin films of bismuth telluride were fabricated on silicon substrates at room temperature using thermal evaporation method. Tellurium (Te) and bismuth (Bi) were deposited on silicon substrate in different ratio of thickness. These films were annealed at 50°C and 100°C. After heat treatment, the thin films attained the semiconductor nature. Samples were studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM) to show granular growth.

Effect of Au on the Performance of Porous Silicon/V2O5 Nanorods Heterojunctions to NO2 Gas

NANO ◽  
2016 ◽  
Vol 11 (07) ◽  
pp. 1650079 ◽  
Author(s):  
Wenjun Yan ◽  
Ming Hu ◽  
Jiran Liang ◽  
Dengfeng Wang ◽  
Yulong Wei ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Porous Silicon ◽  
Room Temperature ◽  
Au Nanoparticles ◽  
Analytical Techniques ◽  
Heating Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

A novel composite of Au-functionalized porous silicon (PS)/V2O5 nanorods (PS/V2O5:Au) was prepared to detect NO2 gas. PS/V2O5 nanorods were synthesized by a heating process of pure vanadium film on PS, and then the obtained PS/V2O5 nanorods were functionalized with dispersed Au nanoparticles. Various analytical techniques, such as field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), have been employed to investigate the properties of PS/V2O5:Au. Herein, the PS/V2O5:Au sample exhibited improved NO2-sensing performances in response, stability and selectivity at room temperature (25[Formula: see text]C), compared with the pure PS/V2O5 nanorods. These phenomena were closely related to not only the dispersed Au nanoparticles acting as a catalyst but also the p-n heterojunctions between PS and V2O5 nanorods. Whereas, more Au nanoparticles suppressed the improvement of response to NO2 gas.

Synthesis of Ti3Si0.4Al0.8C1.8 Solid Solution

2008 ◽  
Vol 368-372 ◽  
pp. 995-997
Author(s):  
Cui Wei Li ◽  
Hong Xiang Zhai ◽  
Yang Zhou ◽  
Shi Bo Li ◽  
Zhi Li Zhang
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Single Phase ◽  
Lattice Parameters ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Powder Mixtures ◽  
X Ray ◽  
Scanning Electron

In this study, free Ti/Si/Al/C powder mixtures with molar ratio of 3:0.4:0.8:1.8 were heated in Argon with various schedules, in order to reveal the possibility for the synthesis of Ti3Si0.4Al0.8C1.8 solid solution powder. X-ray diffraction (XRD) was used for the evaluation of phase identities of the powder after different treatments. Scanning electron microscopy (SEM) was used to observe the morphology of the Ti3Si0.4Al0.8C1.8 solid solution. XRD results showed that predominantly single phase samples of Ti3Si0.4Al0.8C1.8 was prepared after heating at 1400oC for 5 min in Argon and the lattice parameters of Ti3Si0.4Al0.8C1.8 lay between those of Ti3SiC2 and Ti3AlC2.

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