Improvement in Fabrication of Hg-1223 Superconductor by Te-Doping

2000 ◽  
Vol 659 ◽  
Author(s):  
K.K. Yau ◽  
C.C. Lam ◽  
L.J. Shen ◽  
S.H. Li
Keyword(s):  
Critical Temperature ◽  
Vapour Pressure ◽  
Quartz Tube ◽  
Mercury Vapour ◽  
Oxide Superconductors ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
Laboratory Environment ◽  
X Ray ◽  
Copper Oxide Superconductors

ABSTRACTThe sealed quartz tube method is one of the usual methods used for sintering mercury-based copper oxide superconductors. By this method, precursor pellets are inserted into the quartz tube together with certain mass ratio to the reagent sample pellets for controlling the mercury vapour pressure. A certain amount of excess HgO is required to ensure the fabricated sample to have the desired composition. In our research, it was found that if a small amount of TeO2 is added and mixed with the pulverized precursor after first calcination, Hg-1223 superconductors can be fabricated without using the precursor pellet and no excess HgO is required. Thus, the fabrication process can be simplified. As mercury and its oxide are toxic, if no excess Hg is involved, it is safe and good for the laboratory-environment. In this research, some amounts of 0.10 and 0.18 wt% (weigh percentage) of TeO2 were added into the precursor, it is shown that the critical temperature of the fabricated samples is comparable to that of the undoped Hg-1223 samples. For 0.10 wt% of TeO2, the Tc of the as-synthesized sample is about 116.7 K whereas the annealed Te-doped Hg-1223 is about 134.2 K. For 0.18 wt% of TeO2, the Tc of the as- synthesized and annealed samples are 115.8 K and 134.6 K, respectively. The phase structure of samples fabricated in this research has been analyzed by the X-ray diffraction technique. It shows that the Hg-1223 phase is dominated.

Assessment of Laser Effects on the Structure and Electrical Properties of the Compound Bi2-xAgxSr2Ca2Cu3O10+δ Superconducting

2021 ◽  
Vol 19 (11) ◽  
pp. 108-115
Author(s):  
Nihad Ali Shafeek
Keyword(s):  
Critical Temperature ◽  
Hydraulic Press ◽  
Electrical Characteristics ◽  
X Ray Diffraction ◽  
Solid State Method ◽  
X Ray ◽  
Compensation Ratio ◽  
Superconducting Compound ◽  
State Method ◽  
Two Stages

This research contains preparing the superconducting compound Bi2-xAgxSr2Ca2Cu3O10+δ and studying its structural and electrical characteristics. The samples were prepared using the solid-state method in two stages, and different concentrations of x were (x= 0.2,0.4,0.6,0.8) replaced instead of bismuth Bi. Then, using a hydraulic press 9 ton/cm2 and sintering with a temperature of 850°C, the samples were pressed. Next, x-ray diffraction is used to study the structural properties. The study of these samples was presented in different proportions of x values, where x = 0.4 is the best compensation ratio of x. A critical temperature of 1400C and the Tetragonal structure was got. After that, the effect of laser nidinium _ yak (Nd: YAG laser) was used on the compositional. It was found that the temperature value increased, so we got the best critical temperature, which is 142 0C.

Optimization of Structure of Soft Block for Design of Adaptive Polyurethanes

2020 ◽  
Vol 869 ◽  
pp. 273-279
Author(s):  
Marina A. Gorbunova ◽  
Denis V. Anokhin ◽  
Valentina A. Lesnichaya ◽  
Alexander A. Grishchuk ◽  
Elmira R. Badamshina
Keyword(s):  
Mutual Influence ◽  
Glycol Adipate ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Crystallization Conditions ◽  
Crystalline Domains ◽  
Kinetics Of

A synthesis of new di-and triblock polyurethane thermoplastic copolymers containing different mass ratio of two crystallizing blocks - poly (1,4-butylene glycol) adipate and poly-ε-caprolactone diols was developed. Using combination of danamometric analysis, IR-spectroscopy, differential scanning calorimetry and X-ray diffraction, the effect of the soft block composition and crystallization conditions on crystal structure and thermal behavior of the obtained polymers have been studied. For the triblock copolymers we have shown a possibility of control the kinetics of material hardening and final mechanical characteristics due to the mutual influence of polydiols during crystallization. In the result, the second crystallizing component allows to control amount, structure and quality of crystalline domains in polyurethanes by variation of crystallization conditions.

scholarly journals Aktivitas Dan Pemodelan Katalis Silikat Dari Abu Sekam Padi Untuk Konversi Heksana

REAKTOR ◽  
2017 ◽  
Vol 9 (2) ◽  
pp. 1
Author(s):  
D. D. Anggoro
Keyword(s):  
Quartz Tube ◽  
X Ray Diffraction ◽  
X Ray ◽  
Tube Reactor ◽  
Padi Rice

Abu sekam padi  (Rice Hush Ash, RHA) apabila dikalsinasi pada suhu tinggi (500-600 0C) menghasilkan senyawa silikat yang dapat dimanfaatkan untuk beragai proses kimia. Senyawa silikat merupakan senyawa terbesar penyusun abu sekam padi yaitu mencapai ±96,6%. Penelitian pendahuluan menunjukkan bahwa silikat yang dihasilkan dari sekam padi s.ebesar 15%  dari berat sekam padi yang dikalsinasi. Untuk mengetahui struktur silikat yang dihasilkan maka dilakukan analisa dengan menggunakan X-Ray Diffraction (XRD) dengan cara membandingkan diffractogram dari silikat murni . silikat yang dihasilkan kemudian diuji kemampuan daya perengkaha dan aromatisasinya sebagai katalis dalam reaksi heksana dengan menggunakan quartz tube reactor pada suhu 200-300 0C. Dari hasil XRD dapat disimpulkan bahwa abu sekam padi bias digunakan sebagai sumber silikat murni. Uji laboratorium menunjukkan bahwa  silikat yang dihasilkan dari abu sekam padi mempunyai potensi sebagai katalis untuk reaksi perengkahan dan aromatisasi.Kata kunci : abu sekam padi, silikat, perengkahan, aromatisasi

Structural and phase equilibria studies in the system Pt-Fe-Cu and the occurrence of tulameenite (Pt2FeCu)

1985 ◽  
Vol 49 (353) ◽  
pp. 547-554 ◽  
Author(s):  
M. Shahmiri ◽  
S. Murphy ◽  
D. J. Vaughan
Keyword(s):  
Crystal Structure ◽  
Solid Solution ◽  
Critical Temperature ◽  
Grain Boundary ◽  
Phase Region ◽  
X Ray Diffraction ◽  
Two Phase ◽  
Slow Cooling ◽  
X Ray ◽  
Diffraction Patterns

AbstractThe crystal structure and compositional limits of the ternary compound Pt2FeCu (tulameenite), formed either by quenching from above the critical temperature of 1178°C or by slow cooling, have been investigated using X-ray diffraction, transmission electron microscopy, differential thermal analysis and electron probe microanalysis.The crystal structure of Pt2FeCu, established using electron density maps constructed from the measured and calculated intensities of X-ray diffraction patterns of powdered specimens, has the (000) and (½½0) lattice sites occupied by Pt atoms and the (½0½) and (0½½) sites occupied by either Cu or Fe atoms in a random manner. The resulting face-centred tetragonal structure undergoes a disordering transformation at the critical temperature to a postulated non-quenchable face-centred cubic structure. Stresses on quenching, arising from the ordering reaction, are relieved by twinning along {101} planes or by recrystallization along with deformation twinning; always involving grain boundary fracturing.Phase relations in the system Pt-Fe-Cu have been investigated through the construction of isothermal sections at 1000 and 600°C. At 1000°C there is an extensive single phase region of solid solution around Pt2FeCu and extending to the binary composition PtFe. At 600°C the composition Pt2FeCu lies just outside this now reduced area of solid solution in a two-phase field. Comparison of the experimental results with data for tulameenite suggests that some observed compositions may be metastably preserved. The occurrence of fine veinlets of silicate or other gangue minerals in tulameenite is suggested to result from grain boundary fracturing on cooling below the critical temperature of 1178°C and to be evidence of a magmatic origin.

Preparation, Characterization and Hemostatic Properties of Chitosan Caffeates

2019 ◽  
Vol 814 ◽  
pp. 365-371
Author(s):  
Si Tong Lu ◽  
Dong Ying Zhang ◽  
Zhang Hu ◽  
Si Dong Li ◽  
Pu Wang Li
Keyword(s):  
Caffeic Acid ◽  
Freeze Drying ◽  
Water Solubility ◽  
Crystal Form ◽  
Positive Control ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Yunnan Baiyao ◽  
Better Than

In this paper, chitosan and caffeic acid were used as starting materials to prepare chitosan caffeates by reflux-heating and freeze-drying. The structures of chitosan caffeates were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and potentiometric titration. At the same time, the physical properties of chitosan caffeates were tested and the hemostatic properties were evaluated. The results showed that four chitosan caffeates with different mass ratios of chitosan and caffeic acid (1:1, 1:2, 1:4, 1:6) had been successfully prepared, which enhanced the water solubility. FTIR analysis demonstrated that caffeic acid had been successfully grafted onto chitosan chains. XRD showed that the crystal form of chitosan changed to some extent and the chain had some regularity in some directions, but its crystallinity reduced. Chitosan caffeates, particularly mass ratio of 1:1, showed excellent hemostatic properties and even better than chitosan and the positive control (Yunnan Baiyao), which were expected to be developed as an effective biomaterial for hemostasis.

Isomerization of α-Pinene over Alumina-Pillared Montmorillonite

2013 ◽  
Vol 746 ◽  
pp. 49-52 ◽  
Author(s):  
Peng Quan Yao ◽  
Lin Hua Zhu ◽  
Jin Yang ◽  
Tian Si
Keyword(s):  
Basal Spacing ◽  
High Catalytic Activity ◽  
Temperature Reaction ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Pillared Montmorillonite ◽  
Catalytic Isomerization ◽  
Optimum Reaction

In this work, the liquid phase catalytic isomerization of α-pinene over alumina-pillared montmorillonitewas investigated, and the influence of reaction temperature, reaction time and amount of the catalyston the conversion of α-pinenewere discussed systematically, and the optimum reaction conditions forisomerization of α-pineneover alumina-pillared montmorillonitewere obtained. The basal spacing of thealumina-pillared montmorillonite was characterized by X-ray diffraction, and the liquid reactant was separated and identified by gas chromatography. The result showed that alumina-pillared montmorillonite with 1.83nm of basal spacing exhibited a high catalytic activity for the isomerization of α-pinene, and 97.4% conversion of α-pinene was achievedat 373K for 3hwhen the mass ratio of catalyst to α-pinene was 1/10.

scholarly journals Development of 3D Bioactive Scaffolds through 3D Printing Using Wollastonite–Gelatin Inks

Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2420 ◽  
Author(s):  
Filis Curti ◽  
Izabela-Cristina Stancu ◽  
Georgeta Voicu ◽  
Horia Iovu ◽  
Cristina-Ioana Dobrita ◽  
...  
Keyword(s):  
3D Printing ◽  
Bone Repair ◽  
Homogeneous Distribution ◽  
Orthopedic Trauma ◽  
Fish Gelatin ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Bioactive Scaffolds ◽  
Microscopy Images

The bioactivity of scaffolds represents a key property to facilitate the bone repair after orthopedic trauma. This study reports the development of biomimetic paste-type inks based on wollastonite (CS) and fish gelatin (FG) in a mass ratio similar to natural bone, as an appealing strategy to promote the mineralization during scaffold incubation in simulated body fluid (SBF). High-resolution 3D scaffolds were fabricated through 3D printing, and the homogeneous distribution of CS in the protein matrix was revealed by scanning electron microscopy/energy-dispersive X-ray diffraction analysis (SEM/EDX) micrographs. The bioactivity of the scaffold was suggested by an outstanding mineralization capacity revealed by the apatite layers deposited on the scaffold surface after immersion in SBF. The biocompatibility was demonstrated by cell proliferation established by MTT assay and fluorescence microscopy images and confirmed by SEM micrographs illustrating cell spreading. This work highlights the potential of the bicomponent inks to fabricate 3D bioactive scaffolds and predicts the osteogenic properties for bone regeneration applications.

scholarly journals Extraction of alumina from alumina rich coal gangue by a hydro-chemical process

2020 ◽  
Vol 7 (4) ◽  
pp. 192132 ◽  
Author(s):  
Quancheng Yang ◽  
Fan Zhang ◽  
Xingjian Deng ◽  
Hongchen Guo ◽  
Chao Zhang ◽  
...  
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Chemical Process ◽  
Energy Dispersive Spectrometer ◽  
Coal Gangue ◽  
Added Value ◽  
High Alumina ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray

Vast quantities of gangue from coal mining and processing have accumulated over the years and caused significant economic and environmental problems in China. For high added-value utilization of alumina rich coal gangue (ARCG), a mild hydro-chemical process was investigated to extract alumina. The influences of NaOH concentration, mass ratio of alkali to gangue, reaction temperature and reaction time were systematically studied. An alumina extraction rate of 94.68% was achieved at the condition of NaOH concentration 47.5%, alkali to gangue ratio of 6, reaction temperature of 260°C and reaction time of 120 min. The obtained leaching residues were characterized through X-ray diffraction, scanning electron microscopy and energy-dispersive spectrometer. Research confirmed that kaolinite the main alumina-bearing phase of ARCG can be decomposed and transformed to Na 8 Al 6 Si 6 O 24 (OH) 2 (H 2 O) 2 and Ca 2 Al 2 SiO 6 (OH) 2 at relatively low temperature and short reaction time. Additionally, Na 8 Al 6 Si 6 O 24 (OH) 2 (H 2 O) 2 and Ca 2 Al 2 SiO 6 (OH) 2 are unstable and will transform to alumina-free phase NaCaHSiO 4 under the optimal conditions, which is the major reason for high alumina extraction rates.

Synthesis of Biodiesel from Castor Oil Catalyzed by Cesium Phosphotungstate with the Assistance of Microwave

2013 ◽  
Vol 291-294 ◽  
pp. 300-306 ◽  
Author(s):  
Hong Yuan ◽  
Qing Shu
Keyword(s):  
Microwave Radiation ◽  
Castor Oil ◽  
Solid Acid ◽  
Maximum Yield ◽  
Conventional Heating ◽  
Molar Ratio ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Programmed

Two cesium phosphotungstate-derived solid acid catalysts (Cs2.5H0.5PW12 and Cs0.5H2.5PW12) were prepared. The resulting catalysts were characterized by powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), N2 adsorption and desorption isotherm and temperature programmed desorption of ammonia(NH3-TPD). The Cs2.5H0.5PW12 and Cs0.5H2.5PW12 were respectively used to catalyze the tranesterification of castor oil and methanol for the synthesis of biodiesel with the assistance of microwave. Results shown microwave radiation can greatly enhance the transesterification process when compared with conventional heating method. Cs2.5H0.5PW12 showed better catalyst performance than Cs0.5H2.5PW12. A maximum yield of 90% was obtained from the using of 30:1 molar ratio of methanol to castor oil and 15 wt % mass ratio of catalyst to castor oil at 343 K under microwave radiation after 4h.

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