共查询到20条相似文献,搜索用时 31 毫秒
1.
Phase equilibria of the La2 O3 -SrO-CuO system have been determined at 950°C and 10 kbar (1 GPa). Stable phases at the apices of the ternary phase diagram are CuO, La2 O3 , and SrO. Stable intermediate phases are La2 CuO4 in the LaO1.5 -CuO binary and Sr2 CuO3 , SrCuO2 , and Sr14 Cu24 O41 in the CuO-SrO binary. The La2-x Sr x CuO4-δ solid solution is stable where 0.0 ≤ x ≤ 1.3, the La2-x Sr1+x Cu2 O6+δ solid solution is stable where 0.0 ≤ x ≤ 0.2, the La8-x Sr x Cu8 O20-δ solid solution is stable where 1.3 ≤ x ≤ 2.7, the La x Sr14-x -Cu24 O41 solid solution is stable where 0 ≤ x ≤ 6, and the La1+x Sr2-x Cu2 O5.5+δ phase is stable where 0.04 ≤ x ≤ 0.16. The La2 O3 -SrO-CuO phase diagram at 950°C and 10 kbar is almost identical to that determined by other authors at 950°C and 1 atm, in terms of phase stability and solid-solution ranges. 相似文献
2.
Phase equilibria of the La2 O3 –SrO–CuO system have been determined at 950°C at 30 kbar (3 GPa). Stable phases at the apexes of the ternary phase diagram are CuO, La2 O3 , and SrO. Stable intermediate phases are La2 , CuO4 and La2 Cu2 O5 in the LaO1.5 –CuO binary and Sr2 CuO3 , SrCuO2 , and Sr14 Cu24 O41 in the CuO–SrO binary. The La2– x Sr x -CuO4–δ solid solution is stable for 0.00 is ≤ x ≤ 1.29, the La2– x Sr1+ x Cu2 O6+δ solid solution is stable for 0.03 ≤ x ≤0.20, the La2– x Sr x Cu2 O5–δ solid solution is stable for 0.00 ≤ x ≤1.08, and the La x Sr14– x Cu24 O41 solid solution is stable for 0.00 ≤ x ≤ 6.15. The 30 kbar phase diagram differs from the 1 atm (0.1 MPa) and 10 kbar (1 GPa) results principally in the absence of La1– x Sr2+ x Cu2 O5.5+δ as a stable phase and the extended range of the La2– x Sr x Cu2 O5–δ solid solution at 30 kbar. 相似文献
3.
Takayuki Komatsu Michiko Ueta Tomohiro Ohki Ryuji Sato Kazumasa Matusita 《Journal of the American Ceramic Society》1992,75(7):1864-1869
The Ba-doped superconducting (Bi,Pb)2 Sr2- x Ba x Ca2 Cu3 O y and (Bi,Pb)2 Sr2 Ca2- x Ba x Cu3 O y (0 ≦ x ≦ 1.0) were prepared by using a melt-quenching method, and the effect of Ba additions on the glass-forming ability and the crystalline phase was examined. The glass-forming ability was not improved by substitution of Ba for Sr or Ca, and particularly BaPbO3 as well as CaO was observed in the melt-quenched sample of (Bi,Pb)2 SrBaCa2 Cu3 O y . BaPbO3 crystals were precipitated in all glass-ceramics with Ba substituted for Sr or Ca. The partial substitution of Ba substituted for Sr was effective for the formation of the high- T c phase, and (Bi,Pb)2 Sr1.4 Ba0.6 Ca2 Cu3 O y glass-ceramics obtained by annealing at 830°C for 100 h exhibited superconductivity with a T c of 103 K, although BaPbO3 and the low- T c phase were still largely present. 相似文献
4.
Teen-Hang Meen Ying-Chung Chen Ken-Whie Liaw Hung-Duen Yang 《Journal of the American Ceramic Society》1993,76(8):1948-1952
X-ray diffraction patterns show that most samples of Y1-x Prx Ba2 Cu4 O8 examined in the present study contained a single YBa2 Cu4 O8 (1-2-4) superconductive phase for x<0.7.Lattice parameters a and b increased with Pr concentration, suggesting that most of the Pr is trivalent in Y1-x Prx- Ba2 Cu4 O8 . The zero-resistance temperature, T co , decreases monotonically from 80 K at x=0 to 12 K at x=0.65, and superconducting transition widths tend to broaden for x>0. The room-temperature resistivity changes linearly until x=0.7 and increases abruptly at x=-0.75. The critical concentration, xcr , thus was estimated to be 0.7. The effective magnetic moments of Pr in Y 1-x Prx Ba2 Cu4 O8 were 3.63., 3.35, and 3.23, μB for x=0.2, 0.4 and 0.6, respectively. In the R0.8 Pr0.2 Ba2 Cu4 O8 system, the depression of Tc weakly depends on the ionic radius of rare-earth elements. Similarities and differences between Y 1-x Prx Ba2 Cu4 O8 and Y1-x Prx- Ba2 Cu3 O7-y also were noted and are discussed in this paper. 相似文献
5.
Ji-Ping Zhou Charles C. Sorrell Shi-Xue Dou Miles H. Apperley 《Journal of the American Ceramic Society》1991,74(7):1541-1546
The present work describes a new technique to synthesize aligned YBa2 Cu3 O7- x and Ag─YBa2 Cu3 O7- x superconducting composites from Ba- and Cu-deficient compositions (relative to YBa2 Cu3 O7- x ) plus BaCuO2 . For YBa2 Cu3 O7- x , high transition temperature midpoint Tc (91 K), temperature of zero resistivity T 0 (90 K), and critical current density Jc (>3000 A°Cm−2 at 77 K) were achieved by using this technique. This procedure provides the potential for using a reliable and reproducible densification and alignment technique alternative to partial or full melting. The composite is highly aligned, with an average grain size of ∼1 to 2 mm and domains of width greater than 5 mm. The initial phase assemblage consists of YBa2 Cu3 O7- x (123) as the major phase plus YBa2 CuO5 (211) CuO as minor phases. The BaCuO2 is added to the Ba- and Cu-deficient starting composition in order to assist in the formation of a CuO-rich liquid as well as to compensate for the Ba and Cu deficiences in 123. Since the liquid forms at ∼900°C and is compatible with 123, it can be used to facilitate alignment of 123 at ∼930°C. The addition of Ag to the system results in eutectic formation with the (solidified) liquid, substantial filling of the pores during sintering, and improved alignment. 相似文献
6.
Robert S. Roth Claudia J. Rawn John D. Whitler C. K. Chiang Winnie K. Wong-Ng 《Journal of the American Ceramic Society》1989,72(3):395-399
Studies in the Sr-Y-Cu-O and Ba-Sr-Y-Cu-O systems have revealed that Sr will substitute for Ba in (Ba,Sr)2 YCu3 O6+ x up to about 60%. There are no ternary compounds in the Sr-Y-Cu-O system equivalent to the three ternary phases in the Ba system. A new binary phase, "Sr14 Cu24 O41 "(CuO ∼ 63.158 mol%), was found which forms a solid solution with Y2 O3 to a Sr:Y ratio of approximately 2:1. This phase can also incorporate considerable amounts of Ba and Ca and many other large ions. 相似文献
7.
Yoshihiro Kusano Takeyuki Kikuchi Jun Takada Minoru Fukuhara Yasunori Ikeda Zenji Hiroi 《Journal of the American Ceramic Society》1999,82(5):1329-1332
The phase diagram of the BaO(BaCO3 )-CaO-CuO system, especially in the barium-rich region at 900°C in air, was studied. Two new different oxycarbonates were observed: Ba8 Ca16/15 Cu64/15 O11.20 (CO3 )2.66 and a solid-solution series with a chemical composition of Ba2 Ca x + y Cu1+( x /2)- y O2+delta (CO3 )1- z (where 0 ≤ to x ≤ to 2/39 and 0 ≤ to y ≤ to 16 x /5). The oxycarbonate solid solution was formed in a region of the compositional triangle Ba:Ca:Cu (in moles) = (2:0:1)-(39:1:20)-(65:7:28). The solid-solution structure had P 4/ mmm symmetry, with lattice parameters a similar/congruent a p and c similar/congruent 2 a p , where a p represents the perovskite cell. The Ba8 Ca16/15 Cu64/15 O11.20 (CO3 )2.66 compound, which had Pm 3 m symmetry with a lattice parameter a = 0.8116(2) nm, had no chemical-solubility range. 相似文献
8.
The (YBa2 Cu3 )1−x Nax O7–δ system in the range of x = 0–0.8 was investigated. Experimental data suggest that the sodium doping with x 0.26 does not affect the critical transition temperature Tc , and the crystal structure maintains the orthorhombic lattice with a slightly smaller unit cell. However, sodium doping increases the sintering and grain growth kinetics, resulting in a higher superconducting phase volume and an enhanced Meissner effect. It also lowers the processing temperaturel. The experimental data also suggest that the sodium atoms diffuse into the superconducting YBa2 Cu3 O7−δ crystallites, which stabilizes the orthorhombic phase. The transition temperature (ortho-rhombic to tetragonal) in sodium-doped materials increases with the increasing concentration of sodium. 相似文献
9.
Retrograde densification of pelletized calcines and glasses having an approximate (Bi,Pb)2 Sr2 Ca2 Cu3 O10 starting stoichiometry and sintered at ∼850°C can be described by first-order rate equations. Retrograde densification in the calcine precursors was largely due to the development of open pores, and was approximately proportional to the concentration of the (Bi,Pb)2 Sr2 CaCu3 O10 phase. In the glasses, retrograde densification is mainly caused by porosity accompanying the growth of a needlelike Sr─Ca─Cu─O phase, together with (Bi,Pb)2 Sr2 Ca2 Cu3 O10 and (Bi,Pb)2 Sr2 CaCu2 O8 . 相似文献
10.
Sara Bals Jo Verbeeck Gustaaf Van Tendeloo Yi-Lin Liu Jean-Claude Grivel 《Journal of the American Ceramic Society》2005,88(2):431-436
The microstructural and compositional evolution during initial annealing of a superconducting (Bi,Pb)2 Sr2 Ca2 Cu3 O10+δ /Ag tape is studied using quantitative transmission electron microscopy. Special attention is devoted to the occurrence of Pb-rich liquids, which are crucial for the Bi2 Sr2 CaCu2 O8+δ to (Bi,Pb)2 Sr2 Ca2 Cu3 O10+δ transformation. Ca and/or Pb-rich (Bi,Pb)2 Sr2 CaCu2 O8+δ grains dissolve into a liquid, which reacts with Ca-rich phases to increase the liquid's Ca-content. This leads to (Bi,Pb)2 Sr2 Ca2 Cu3 O10+δ formation. Apparently, a Ca/Sr ratio of around 1 is sufficient to keep (Bi,Pb)2 Sr2 Ca2 Cu3 O10+δ nucleation going. It is confirmed that Ag particles are transported from the Ag-sheath into the oxide core by the liquid and not by mechanical treatment of the tape. 相似文献
11.
The phase relations in the systems MgO-Y2 O3 -ZrO2 and CaO-MgO-ZrO2 were established at 1220° and 1420°C. The system MgO-Y2 O3 -ZrO2 possesses a much-larger cubic ZrO2 solid solution phase field than the system CaO-MgO-ZrO2 at both temperatures. The ordered δ phase (Zr3 Y4 O12 ) was found to be stable in the system ZrO2 -Y2 O3 at 1220°C. Two ordered phases φ1 (CaZr4 O9 ) and φ2 (Ca6 Zr19 O44 ) were stable at 1220°C in the system ZrO2 -CaO. At 1420°C no ordered phase appears in either system, in agreement with the previously determined temperature limits of the stability for the δ, φ1 , and φ2 phases. The existence of the compound Mg3 Yz O6 could not be confirmed. 相似文献
12.
Ji-Ping Zhou Charles C. Sorrell Antony J. Bourdillon Shi-Xue Dou 《Journal of the American Ceramic Society》1990,73(7):2147-2150
In the system Y-Ba-Cu-O, partial melting of peritectically decomposing YBa2 Cu3 O7- x (123) was used to produce a bulk material of high critical current density when the material was aligned. The liquid formation mechanism and its relation to reaction with alumina refractory was studied. A previously unreported phase of the approximate stoichiometric ratio Y:Ba:Cu:Al = 1:4:1:1 (YBa4 CuAlO8 ) was detected. The crystal structure was determined to be tetragonal, with lattice parameters a 0 = b 0 = 1.651 nm, c 0 = 1.793 nm. The 1411 phase bears a close structural relationship to BaCuO2 . 相似文献
13.
Anita Fossdal Mari-Ann Einarsrud Tor Grande 《Journal of the American Ceramic Society》2005,88(7):1988-1991
The phase relations in the pseudo-ternary system La2 O3 –SrO–Fe2 O3 have been investigated in air. Isothermal sections at 1100° and 1300°C are presented based on X-ray diffraction and thermal analysis of annealed samples. Extended solid solubility was observed for the compounds Sr n +1− v La v Fe n O3 n +1−δ ( n =1, 2, 3, and ∞) and Sr1− x La x Fe12 O19 , while only limited solubility of La in Sr4− z La z Fe6 O13±δ was observed. At high Fe2 O3 content, a liquid with low La2 O3 content was stable at 1300°C. 相似文献
14.
Stefanie Kaesche Peter Majewski Fritz Aldinger 《Journal of the American Ceramic Society》1999,82(1):197-202
Phase equilibria of the quasi-quaternary system BiO1.5 –SrO-YO1.5 –CuO have been studied at a temperature of 950°C in air, with special regard to the 1212 phase. The 1212 phase reveals only very small changes in the cation ratio. Single-phase samples exist for (Bi0.24–0.36 Cu0.42-0.55 )–Sr2 Y1.27 Cu2 O y compositions. The bismuth-rich composition of the 1212 phase is in thermodynamic equilibrium with a liquid and the 2212 phase, whereas the copper-rich composition is in equilibrium with five other phases. The influence of combined calcium and lead doping also has been studied. Exceeding the calcium saturation of the 1212 phase increases the amount of 2212 as a secondary phase. Single-phase 1212 samples do not show any superconductivity in either the as-prepared or the post-annealed state. The only compositions with bulk superconductivity are those with calcium and lead doping after annealing at a temperature of 980°C. The superconductivity is attributed to the 2212 phase crystallizing from the melt during slow cooling. 相似文献
15.
Two cubic pyrochlore phases exist in the system ZnO–Bi2 O3 –Sb2 O5 . Neither has the supposed "ideal" stoichiometry, Zn2 Bi3 Sb3 O14 . One, P 1 , is a solid solution phase, Zn2+ x Bi2.96−( x − y ) Sb3.04− y O14.04+δ where 0< x <0.13(1), 0< y <0.017(2) and a =10.4285(9)−10.451(1) Å. The other, P 2 , is a line phase, Zn2 Bi3.08 Sb2.92 O13.92 with a =10.462(2) Å. Subsolidus phase relations at 950°C involving phases P 1 and P 2 in the ZnO–Bi2 O3 –Sb2 O5 phase diagram have been determined. 相似文献
16.
Yusuke Kaminaga Hisanori Yamane Takahiro Yamada 《Journal of the American Ceramic Society》2007,90(6):1917-1920
Compounds in a CaO–Y2 O3 –SnO2 system were prepared by a solid-state reaction at 1673 K. The phase relation in this system was investigated by powder X-ray diffraction. Besides the previously reported ternary compounds, CaSnO3 , Ca2 SnO4 , Y2 Sn2 O7 , and a quaternary compound Ca0.4 Y1.2 Sn0.4 O3 , solid-solution series of Ca2− x Y2 x Sn1− x O4 with 0≤ x ≤0.5, and Ca1− y Y2 y Sn1− y O3 with 0≤ y ≤0.2 and 0.95≤ y ≤1.0 were found. The cell parameters of these solid-solution series were refined. The changes of rhombohedral cell parameters in the samples prepared in the range 0.565< y <0.714 of Ca1− y Y2 y Sn1− y O3 suggested the existence of solid solutions of Ca0.4 Y1.2 Sn0.4 O3 , although their single phases could not be prepared, except at y =0.6. 相似文献
17.
The cation solubility limits of the n = 2 and n = 3 superconducting phases in the Bi2 (Sr x Ca1 − x ) n +1 Cu n O y system were established along tie lines with compatible phases via electron probe microanalysis on bi- (or poly-) phasic samples prepared at 860°C. Pb additions (15 mol% of the Bi content) were used to facilitate formation of the n = 3 phase. In each case football-shaped volumes in composition space were established as the solubility limits which bordered on the nominal compositions 2212 or 2223 (Bi:Sr:Ca:Cu) with the long axis parallel to the Sr-Ca side of the quaternary (i.e., Sr-to-Ca intersolubility) but also extending toward Bi and Cu. This means that, for the most part, the superconducting phases are alkaline-earth deficient relative to the ideal 2212 and 2223 compositions. The Pb content in the 2223 phase is typically 10% of the Bi content. T c variations could be correlated with variations in Sr or (Sr + Bi) content and the length of the c -axis parameter. 相似文献
18.
Mukesh K. Agarwala David L. Bourell Chadee Persad 《Journal of the American Ceramic Society》1992,75(7):1975-1977
Fine, homogeneous, dual-phase Ag–YBa2 Cu3 O7– x composite powders were prepared by a simple colloidal sol–gel coprecipitation technique that was previously used for synthesis of single-phase YBa2 Cu3 O7– x . Samples containing up to 60 wt% silver were synthesized. Silver neither reacted with nor degraded the YBa2 Cu3 O7– x . The presence of silver was found to aid the oxygenation of the precursor during calcination to form orthorhombic YBa2 Cu3 O7– x . Measurements made by ac magnetic susceptibility showed no significant degradation in transition temperature for samples containing up to 40 wt% silver. 相似文献
19.
Debao Zhang Baoyu Chen Zhuping Liu Shunguang Li Lili Hu 《Journal of the American Ceramic Society》2004,87(12):2228-2231
Er3+ -doped sodium lanthanum aluminosilicate glasses with compositions of (90− x )(0.7SiO2 ·0.3Al2 O3 )· x Na2 O·8.2La2 O3 · 0.6Er2 O3 ·0.2Yb2 O3 ·1Sb2 O3 (in mol%) ( x = 12, 20, 24, 40, 60 mol%) were prepared and their spectroscopic properties were investigated. Judd–Ofelt analysis was used to calculate spectroscopic properties of all glasses. The Judd–Ofelt intensity parameter Ω t ( t = 2, 4, 6) decreases with increasing Na2 O. Ω2 decreases rapidly with increasing Na2 O while Ω4 and Ω6 decrease slowly. Both the fluorescent lifetime and the radiative transition rate increase with increasing Na2 O. Fluorescence spectra of the 4 I 13/2 to 4 I 15/2 transition have been measured and the change with Na2 O content is discussed. It is found that the full width at half-maximum decreases with increasing Na2 O. 相似文献
20.
Mari Lou Balmer Fred F. Lange Vikram Jayaram Carlos G. Levi 《Journal of the American Ceramic Society》1995,78(6):1489-1494
Aqueous mixtures of zirconium acetate and aluminum nitrate were pyrolyzed and crystallized to form a metastable solid solution, Zr1- x Al x O2− x /2 ( x < 0.57). The initial, metastable phase partitions at higher temperatures to form two metastable phases, viz., t −ZrO2 +γ-Al2 O3 with a nano-scale microstructure. The microstructural observations associated with the γ- →α-Al2 O3 phase transformation in the t -ZrO2 matrix are reported for compositions containing 10, 20, and 40 mol% A12 O3 . During this phase transformation, the α-Al2 O3 grains take the form of a colony of irregular, platelike grains, all with a common crystallographic orientation. The plates contain ZrO2 inclusions and are separated by ZrO2 grains. The volume fraction of A12 O3 and the heat treatment conditions influence the final microstructure. At lower volume fractions of A12 O3 , the colonies coarsen to single, irregular plates, surrounded by polycrystalline ZrO2 . Interpenetrating microstructures produced at high volume fractions of A12 O3 exhibit very little grain growth for periods up to 24 h at 1400°C. 相似文献