scholarly journals Phase, Microstructure, Thermochromic, and Thermophysical Analyses of Hydrothermally Synthesized W-Doped VO2 Nanopowder

2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Hamdi Muhyuddin Barra ◽  
Soo Kien Chen ◽  
Nizam Tamchek ◽  
Zainal Abidin Talib ◽  
Oon Jew Lee ◽  
...  
Keyword(s):  
Transition Temperature ◽  
Thermophysical Properties ◽  
Vanadium Dioxide ◽  
X Ray Diffraction ◽  
Abrupt Increase ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Commercial Use ◽  
Elemental Doping ◽  
W Doping

Vanadium dioxide (VO2) has great potential as an intelligent architectural glazing system as it can control the amount of light, heat, and solar energy relative to the temperature in the environment. However, the applicability of VO2 for commercial use is yet to be realized because its phase transition temperature (τc) of ∼68°C is too high for use in buildings. A proven strategy to lower its τc is by elemental doping. Hence, in this study, hydrothermal synthesis of nanostructured VO2 was carried out with the introduction of tungsten (W) as a dopant. Furthermore, the effects of W doping on the structural, thermochromic, and thermophysical properties of VO2 were examined. Using X-ray diffraction (XRD), it was found that the addition of W atoms affected the VO2 lattice since the crystal structure of VO2 was changed from monoclinic to tetragonal rutile. Subsequently, this influenced the thermochromic behavior of the prepared VO2. Based on the differential scanning calorimetry (DSC), doping with tungsten resulted in a significant decrease in τc from 66.47°C to as low as 31.64°C. Moreover, W doping affected the thermophysical properties of the samples. Accordingly, an abrupt increase in the thermal conductivities of the doped samples was observed across the transition temperature.

Influence of Gd Addition on the Structure and Capability of Ni-Mn-In Metamagnetic Shape Memory Alloys

2012 ◽  
Vol 535-537 ◽  
pp. 950-953
Author(s):  
Li Na Bai ◽  
Gui Xing Zheng ◽  
Zhi Jian Duan ◽  
Jian Jun Zhang
Keyword(s):  
Differential Scanning Calorimetry ◽  
Magnetic Properties ◽  
Magnetic Property ◽  
Transition Temperature ◽  
Martensitic Transformation ◽  
Room Temperature ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray

The influences of Gd concentration on martensitic transformation and magnetic properties of NiMnIn alloys were investigated by differential scanning calorimetry (DSC) , vibrating sample magnetometry (VSM), X-ray diffraction (XRD) and etc. It is Observed through the experiment: the addition of Gd enhances martensite transition temperature;X-ray diffraction analysis of experimental alloys is revealed that to the mixture is martensite and austenite at room temperature; content of Gd is not proportional to the improvement of magnetic property.

The Crystal Structures at 10 K of the Trigonal Salts KMIII(NH3)6(ClO4)2Cl2, MIII = Os and Cr, and the Possibility of Phase Transitions

1999 ◽  
Vol 52 (3) ◽  
pp. 219 ◽  
Author(s):  
Philip A. Reynolds ◽  
Brian N. Figgis ◽  
Alexander N. Sobolev
Keyword(s):  
Differential Scanning Calorimetry ◽  
Transition Temperature ◽  
Crystal Structures ◽  
Low Temperatures ◽  
Simple Structure ◽  
Alkali Metal Cations ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Threefold Axis ◽  
X Ray

The crystal structures of KOs(NH3)3(ClO4)2Cl2 and KCr(NH3)6(ClO4)2Cl2 were determined at 10 K by X-ray diffraction, and for the osmium salt also at 293 K. At 293 K the osmium salt is trigonal, space group R 3m, with the same simple structure as others of this class of double salt. At 10 K, in agreement with previous radius ratio predictions, both crystals are best described as remaining R 3m. All previously studied members, with larger alkali metal cations, are twinned R 3 at low temperatures, with small, symmetry-breaking rotations of the hexaamminemetal(III) and perchlorate ions about the threefold axis. Differential scanning calorimetry on CsRu(NH3)6(ClO4)2Cl2 suggests that the R 3m to R 3 change is very extended in temperature with only a small discontinuity at the transition temperature.

Preparation of Tungsten-Doped VO2 (M) Nanoparticles through Sol-Gel Method and Hydrothermal Synthesis

2014 ◽  
Vol 881-883 ◽  
pp. 960-963 ◽  
Author(s):  
Ji Qi ◽  
Bin Zhao ◽  
Naisen Yu ◽  
Chen Niu ◽  
Guan Gran Sun
Keyword(s):  
Phase Transition ◽  
Vanadium Dioxide ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method ◽  
New Process ◽  
Scanning Electron

A new process was developed for synthesizing tungsten-doped vanadium dioxide VO2(M) from ammonium metavanadate. The process includes obtaining V2O5by pyrolysing NH4VO3, doping tungsten in V2O5by sol-gel method, and reducing V2O5to VO2(M) with hydrazine by hydrothermal method. X-ray diffraction (XRD), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) were applied to characterizing the product. The experimental results indicated that tungsten doped VO2(M) nanoparticles were successfully synthesized. The product VO2(M) presents mainly rod-like and block-like morphology. The phase transition temperature decreases with tungsten doped amount increasing, the phase transition takes place over the range from 36.23°C to 62.16°C and the largest enthalpy of the phase transition is 16.24J/g.

Structural Phase Transition of Tungsten-Doped Vanadium Dioxide Nanopowders Prepared by Thermolysis

2008 ◽  
Vol 8 (3) ◽  
pp. 1417-1421 ◽  
Author(s):  
Zifei Peng ◽  
Wei Jiang ◽  
Heng Liu
Keyword(s):  
Phase Transition ◽  
Differential Scanning Calorimetry ◽  
Transition Temperature ◽  
Vanadium Dioxide ◽  
Structural Phase ◽  
Hysteresis Loops ◽  
Tungstic Acid ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Transmission Electron

Tungsten-doped vanadium dioxide (VO2) nanopowders were prepared by thermolysis of (NH4)5[(VO)6(CO3)4(OH)9] · 10H2O at low temperature, with active white powdery tungstic acid used as a substitutional dopant. The composition and microstructure of the powders were examined by X-ray diffraction, transmission electron microscope, and differential scanning calorimetry. The change in electrical resistance due to the S–M transition was measured from 0 to 150 °C by the four-probe method. Hysteresis loops and differential scanning calorimetry analysis of the samples indicated that the phase-transition temperature of VO2 nanopowders was 67.15 °C. For tungstendoped VO2 nanopowders, the temperature was reduced to 26.46 °C. After sintering the nanopowders, Tc rose from 26.46 °C to 34.85 °C with the sizes increasing to the bulk. A significant direct correlation between particle size and Tc was confirmed. The results indicated that white powdery tungstic acid is exceptionally effective as a dopant for reducing transition temperature.

scholarly journals Structural, Thermal and Magnetic Properties of Ga Excess Ni-Mn-Ga

2009 ◽  
Vol 635 ◽  
pp. 43-47 ◽  
Author(s):  
Sanjay Singh ◽  
S. Bhardwaj ◽  
A.K. Panda ◽  
V.K. Ahire ◽  
Amitava Mitra ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Magnetic Properties ◽  
Transition Temperature ◽  
Martensitic Transition ◽  
Martensitic Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ga Doping ◽  
Heat Of Transformation

The martensitic transition and the ferro- to paramagnetic transition have been studied in a series of Ga excess Ni-Mn-Ga specimens [Ni2-xMnGa1+x (0.4≤ x≤ 0.9)] by differential scanning calorimetry and magnetization measurements. The martensitic transition exhibits a hysteresis whose width is similar to Ni2MnGa, indicating that the transition is thermoelastic. The latent heat of transformation is comparable with other Ni-Mn-Ga alloys. A substantial increase in the martensitic transition temperature is observed due to Ga doping. Interestingly, the x-ray diffraction pattern of all the compositions studied show a modulated martensitic structure in the martensitic phase.

Crystal forms and phase transformation of 1,5-pentanediamine-terephthalate: a bio-based nylon 5T monomer

2020 ◽  
Vol 76 (4) ◽  
pp. 524-533
Author(s):  
Zihan Li ◽  
Pengpeng Yang ◽  
Haodong Liu ◽  
Jun Liu ◽  
Sha Zhu ◽  
...  
Keyword(s):  
Transition Temperature ◽  
Water Activity ◽  
Raw Material ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Phase Form ◽  
Crystal Forms ◽  
X Ray ◽  
Thermodynamic Conditions ◽  
Biomass Resources

Nylon 5T is one of the bio-based nylons, its raw material 1,5-pentanediamine is derived from biomass resources and produced by biological methods. 1,5-pentanediamine-terephthalate (PDA-TPA) is the monomeric salt for nylon 5T polymerization, and its own product quality has a significant impact on the performance of nylon 5T. PDA-TPA was prepared by anti-solvent crystallization in this study. It exists in two solid forms, a monohydrate [form (I)] and an anhydrous phase [form (II)]. The transition temperature of the two phases was around 65°C in the given ethanol–water binary (7:1) mixture. The characterization of monohydrate and anhydrate phases regarding structures and stabilities was carefully carried out using powder X-ray diffraction, single crystal X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, hot-stage microscopy and Fourier transform infrared spectroscopy. The relationship between the molecular interactions of monohydrate and anhydrate phases under different packing architectures and their thermal behaviours was analysed and established. In addition, the relationships between the structures and thermal behaviours for the two solid forms were analysed and established. In addition, the effect of solvent on phase conversion, the relationships between the temperature and water activity, as well as the relative stability of monohydrate and anhydrate phases under different thermodynamic conditions, were investigated by solid–solid transformation and solvent-mediated transformation experiments. It was obvious that the transition temperature of monohydrate and anhydrate phases of PDA-TPA was significantly influenced by water activity, and the larger the value of water activity is, the higher is the transition temperature. These studies give insight into the transformation of nylon 5T monomer salt and contribute to the control of target crystal preparation.

Structure and Low Melting Property of Vanadate Tellurite Glass

2010 ◽  
Vol 663-665 ◽  
pp. 1229-1233 ◽  
Author(s):  
Shi Yong Luo ◽  
Wen Cai Xu ◽  
Xin Lin Zhang ◽  
Li Xia Huo
Keyword(s):  
Differential Scanning Calorimetry ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Tellurite Glass ◽  
Melting Process ◽  
Glass Frit ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray

The glasses (80-x)TeO2·xV2O5·20MO (M=Sn, Bi, Ca, Na and K) had been examined as potential replacements for PbO-based glass frits with low firing temperature. The glasses with TeO2 0-44 mol%, and V2O5 39-82 mol% are not suitable for glass frit since they are easy to crystallize. The glasses with the content of the TeO2 54-74 mol%, and the V2O5 9-29 mol% were investigated by differential scanning calorimetry, X-ray diffraction, infrared spectra and fluidity evaluation experiments. The glasses possess appropriate fluidity and do not crystallize in the re-melting process at 723-753 K. The glass transition temperature of the glasses is at 544-578 K. The structure of the glasses is layer upon layer mainly connected by the structure units of [VO4] and [TeO3]. Other modifier ions locate mainly between the layers. The isolated V=O band from the VO5 bipyramids is not occurred in the vitreous structure of the glasses.

Fabrication and study the effect of the laser on the properties of the compound Tl2-xHgxBa2-ySryCa2Cu3O10+δ superconductor

2018 ◽  
pp. 168
Author(s):  
A. Kareem Dahash Ali ◽  
Nihad Ali Shafeek
Keyword(s):  
Transition Temperature ◽  
Solid State ◽  
Hydrostatic Pressure ◽  
Electrical Properties ◽  
Co2 Laser ◽  
Temperature Shift ◽  
Unit Cell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structural And Electrical Properties

This study included the fabrication of    compound (Tl2-xHgxBa2-ySryCa2Cu3O10+δ) in a manner solid state and under hydrostatic pressure ( 8 ton/cm2) and temperature annealing(850°C), and determine the effect of the laser on the structural and electrical properties elements in the compound, and various concentrations of x where (x= 0.1,0.2,0.3 ). Observed by testing the XRD The best ratio of compensation for x is 0.2 as the value of a = b = 5.3899 (A °), c = 36.21 (A °) show that the installation of four-wheel-based type and that the best temperature shift is TC= 142 K  .When you shine a CO2 laser on the models in order to recognize the effect of the laser on these models showed the study of X-ray diffraction of these samples when preparing models with different concentrations of the values ​​of x, the best ratio of compensation is 0.2 which showed an increase in the values ​​of the dimensions of the unit cell a=b = 5.3929 (A °), c = 36.238 (A°). And the best transition temperature after shedding laser is TC=144 K. 

Studies on the Preparation, Characterization and Solubility of -Cyclodextrin-Roxythromycin Inclusion Complexes

2009 ◽  
Vol 2 (2) ◽  
pp. 523-530
Author(s):  
D. Nagasamy Venkatesh ◽  
S. Karthick ◽  
M. Umesh ◽  
G. Vivek ◽  
R.M. Valliappan ◽  
...  
Keyword(s):  
Dissolution Rate ◽  
Inclusion Complexes ◽  
Phase Solubility ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ir Studies ◽  
Poorly Soluble ◽  
Poorly Soluble Drug

Roxythromycin/ β-cyclodextrin (Roxy/ β-CD) dispersions were prepared with a view to study the influence of β-CD on the solubility and dissolution rate of this poorly soluble drug. Phase-solubility profile indicated that the solubility of roxythromycin was significantly increased in the presence of β-cyclodextrin and was classified as AL-type, indicating the 1:1 stoichiometric inclusion complexes. Physical characterization of the prepared systems was carried out by differential scanning calorimetry (DSC), X-ray diffraction studies (XRD) and IR studies. Solid state characterization of the drug β-CD binary system using XRD, FTIR and DSC revealed distinct loss of drug crystallinity in the formulation, ostensibly accounting for enhancement of dissolution rate.

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