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1.
Some effects of CaO, Na2 O, Sb2 O3 , and ZrO2 additions on Li0.3 Zn0.4 Fe2.3 O4 ferrite were studied to improve its density and other material properties. The densification behavior of the ferrite depended on the amount and type of additive. A relative density of ∼98.5% was achieved with the addition of CaO. The grain size decreased with the addition of Na2 O, CaO, and Sb2 O3 . The permeability and electrical resistivity increased with additives. CaO remarkably increased resistvity, whereas, ZrO2 increased permeability. Na2 O and Sb2 O3 increased the Curie temperature, whereas CaO and ZrO2 decreased it. These effects were attributed to mainly additive segregation on the grain boundaries, which suppressed grain-size development during the sintering of lithium zinc ferrite. 相似文献
2.
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
3.
E. F. RIEBLING 《Journal of the American Ceramic Society》1974,57(9):373-377
Ternary Na2 O.Sb2 O3 .GeO2 glasses (with various [Na]/[Na + Sb] ratios) that contained ≥65 mol% GeO2 were prepared. Their densities (volumes), refractive indices, and infrared spectra were determined and their colors noted. The ternary glasses with ≥88 mol% GeO2 exhibit nearly additive volumes, refractivities, and frequencies for the main Ge-O vibration. Ternary glasses with lesser amounts of GeO2 exhibit a variety of behaviors, depending on the [Na]/[Na + Sb] ratio. Small amounts of Sb2 O3 cause significant volume and refraction deviations, as well as changes in νGe-O , that can be associated with gradual elimination of GeO6 octahedra. All the information supports a model for the glasses with 65 to 88 mol% GeO2 that involves a degree of depolymerization that is greater when Na2 O and Sb2 O3 are present together than when either is present alone. 相似文献
4.
Sashi Tandon Ranchhor D. Agrawal Madan L. Kapoor 《Journal of the American Ceramic Society》1994,77(4):1032-1036
The viscosity of sodium borate slags at high Na2 O concentrations (37.3 to 49.4 mol%) and high temperatures (1000° to 1300°C) follows an Arrhenius-type relationship. This relationship was also observed for sodium borate slags (mass% Na2 O/mass% B2 O3 = 0.86) containing CaO and CaF2 for the same temperature range. There has been a reduction in viscosity of the sodium borate slags (mass% Na2 O3 mass% B2 O = 0.53 to 0.86) with increase in Na2 O concentration. On adding CaO (10 to 50 mass%) to the sodium borate slag (mass% Na2 O/mass% B2 O3 = 0.86), the viscosity increased considerably, while an addition of CaF2 (S to 15 mass%) to the slag (30.9 mass% Na2 O3 35.8 mass% B2 O3 , 33.3 mass% CaO) decreased the viscosity. The average activation energies of Na2 O─B2 O3 , Na2 O─B2 O3 ─CaO3 and Na2 O─B2 O3 ─CaO─CaF2 slag systems have been estimated as 14.6, 124.7, and 41.4 kJ/mol, respectively, for the given composition ranges and 1000° to 1300°C temperature range. 相似文献
5.
Phase equilibria data, obtained both by differential thermal analysis and by quenching, are presented for the system Na2 O-Nb2 O5 . Five compounds corresponding to the formulas 3Na2 O.1Nb2 06 , lNa2 O. 1Nb2 O5 , lNa2 O 4Nb2 O6 , lNaz O.7Nb2 O5 , and lNa2 O. 10Nb2 O6 have been found. The compound 3Naz 0.lNb2 O5 melts congruently at 992°C. The compounds 1Na2 O. 4Nb2 O6 , lNa2 O.7Nb2 O, and 1Na2 O. 1Onb2 O5 melt incongruently at 1265°, 1275°, and 1290°C., respectively. The well-known perovskite structure phase NaNbO3 was found to melt congruently at 1412°C. The transition temperatures in NaNbO5 were checked by thermal analysis and only the major structural changes at 368° and 640°C. could be detected. A new disordered form of NaNbO3 could be preserved to room temperature by very rapid quenching. 相似文献
6.
Phase relations in the system Na2 O· Al2 O3 -CaO· Al2 O3 -Al2 O3 at 1200°C in air were determined using the quenching method and high-temperature X-ray diffraction. The compound 2Na2 O · 3CaO · 5Al2 O3 , known from the literature, was reformulated as Na2 O · CaO · 2Al2 O3 . A new compound with the probable composition Na2 O · 3CaO · 8Al2 O3 was found. Cell parameters of both compounds were determined. The compound Na2 O · CaO-2Al2 O3 is tetragonal with a = 1.04348(24) and c = 0.72539(31) nm; it forms solid solutions with Na2 O · Al2 O3 up to 38 mol% Na2 O at 1200°C. The compound Na2 O · 3CaO · 8Al2 O3 is hexagonal with) a = 0.98436(4) and c = 0.69415(4) nm. The compound CaO · 6Al2 O3 is not initially formed from oxide components at 1200°C but behaves as an equilibrium phase when it is formed separately at higher temperatures. The very slow transformation kinetics between β and β "-Al2 O3 make it very difficult to determine equilibrium phase relations in the high-Al2 O3 part of the diagram. Conclusions as to lifetime processes in high-pressure sodium discharge lamps can be drawn from the phase diagram. 相似文献
7.
CECIL M. JONES II 《Journal of the American Ceramic Society》1971,54(7):347-349
A technique for growing α-Al2 O3 crystals is described in which Na2 O·11Al2 O3 is dissolved in a liquid of composition Na2 O·4TiO2 ·3Al2 O3 . Alpha Al2 O3 is precipitated as Na2 O evaporates from the system; Na2 O·11Al2 O3 serves as a source of Al2 O3 , and Na2 O in the liquid. The content of solids in the mixture is always such that it does not melt completely. The size of the α-Al2 O3 crystals grown is related to the Na2 O content of the composition. Crystals as large as 4000 by 3000 μm in the α-axis direction and 500 μm in the c -axis direction have been grown. 相似文献
8.
Subsolidus phase relations in the system Na2 O-Bi2 O3 -TiO2 at 1000°C were investigated by solid-state reaction techniques and X-ray diffraction methods. Five ternary compounds were observed in the system: Na0.5 Bi4.5 Ti4 O15 ; Na0.5 Bi0.5 TiO3 ; a cubic pyrochlore solid solution composed of xNa2 O.25Bi2 O3 .(75−;x) TiO2 where x is 2.5 to 3.75; a new compound Na0.5 Bi8.5 Ti7 O27 indexed with the orthorhombic cell of a = 5.45, b = 5.42, and c = 36.8 Å; and an unidentified phase with the probable composition NaBiTi6 O14 . 相似文献
9.
The binary isopleth Na2 O.B2 O3 -SiO2 of the Na2 O-B2 O3 SiO2 ternary system has been investigated. A phase diagram is presented based upon data from differential thermal analysis studies of prepared glasses and direct observation of the melting behavior using solid-state video imaging. Phase equilibria relations in the Na2 O-B2 O3 -SiO2 ternary system have been reassessed by combining information from this study with existing data from the literature. A revised liquidus surface for the ternary is presented in which the form of the isotherms is updated. 相似文献
10.
BURNHAM W. KING 《Journal of the American Ceramic Society》1954,37(5):238-242
It was first shown that the enamel slips which have the best suspnding characteristics contain equal amounts of Na2 O and B2 O3 and at least a moderate amount of NaF. The solubilities of mixtures of Na2 O, NaF, and B2 O3 were then investigated. The pH of these solutions and the primary crystalline phases separating on evaporation also were determined. The solubility data obtained at room temperature were summarized. When the solutions were evaporated, NaF was the first crystalline phase to separate from a large proportion of the mixtures investigated. It was concluded that the desirable handling characteristics of enamels whose mill liquors contain the proper proportion of Na2 O, NaF, and B2 O3 are not due to the formation of complex salts but to the following combination of properties: (1) the presence of salts with a moderate solubility which changes very slightly with temperature, (2) a moderate pH of about 10 in a probably well-buffered solution, (3) a relatively stable crystalline material, NaF, as a primary phase, and (4) a secondary phase which crystallizes slowly with relatively little shrinkage. 相似文献
11.
The standard Gibbs free energies of formation of CuAlO2 and CuAl2 O4 were determined in the range 700° to 1100°C, using emf measurements on the galvanic cells (1) Pt,CuO +] Cu2 O/CaO-ZrO2 /O2 ,Pt; (2) Pt,Cu +] CuAlO2 +] Al2 O3 /CaO-ZrO2 / Cu +] Cu2 O,Pt; and (3) Pt,CuAl2 O4 +] CuAlO2 +]Al2 O3 /CaO-ZrO2 /O2 ,Pt. The results are compared with published information on the stability of these compounds. The entropy of transformation of CuO from tenorite to the rock-salt structure is evaluated from the present results and from earlier studies on the entropy of formation of spinels from oxides of the rock-salt and corundum structures. The temperatures corresponding to 3-phase equilibria in the system Cu2 O-CuO-Al2 O3 at specified O2 pressures calculated from the present results are discussed in reference to available phase diagrams. 相似文献
12.
Alumina and gallia were substituted separately for Na2 O in amounts of 0.2, 0.5, 1.0, 1.5, 2.0, and 3.0 wt% in three Na2 O-SiO2 glass compositions (82, 84, and 86 wt% SiO2 ) within the immiscibility region. The immiscibility regions for each system extend to ∼1.5 mol% of the added oxide. In general, the addition reduced the immiscibility temperature ( T m ), but at the edge of the immiscibility region (82% SiO2 ) the Na2 O loss effect initially increased T m . A structural model of the miscibility of Al2 O3 added to silicate glasses is presented. 相似文献
13.
Bing Zhang Qi Chen Li Song Huiping Li Fengzhen Hou 《Journal of the American Ceramic Society》2008,91(6):2036-2038
The influence of 0–16 mol% Sb2 O3 substitution for P2 O5 on the properties of ZnO–P2 O5 glasses has been investigated. It was shown that Sb2 O3 could participate in the glass network and thermal stability of the glasses decreased with increasing Sb2 O3 content. Glass transition temperature T g , softening temperature T s , and water durability all decreased firstly (up to 6 mol% Sb2 O3 added) and then increased. Substitution of 12 mol% Sb2 O3 led to a 16°C decrease in T g and 30°C decrease in T s , and weight loss of the glass was only 0.42 mg/cm2 , which is ∼11 times lower than that of the glass without Sb2 O3 after immersion in deionized water at 90°C for 1 day. The glass containing 12 mol% Sb2 O3 might be a substitute for Pb-based glasses in some applications. 相似文献
14.
Takashi Wakasugi Rikuo Ota Jiro Fukunaga 《Journal of the American Ceramic Society》1992,75(11):3129-3132
In order to evaluate the crystallization tendency of glasses, the ratio of the crystallization temperature to the liquidus temperature ( T c / T L ) was obtained by DTA measurement for the Na2 O–B2 O3 and Na2 O–B2 O3 –Al2 O3 systems. The critical cooling rate for glass formation ( Q *) was also measured. The measurements were performed in the composition range of (100 − x )Na2 O–( x )B2 O3 , ( x = 25–35 and 60–100 mol%), and (100 − y )0.5Na2 O·0.5B2 O3 −( y )Al2 O3 , ( y = 6–34 mol%). The relationship between T c / T L and Q * was discussed. A linear relationship between T c / T L and log Q * for these systems was found. Furthermore, the relationship between T c / T L and Q * was verified by computer simulation based on the crystallization kinetics of glass or supercooled liquid. 相似文献
15.
Steve W. Martin Emanuel I. Cooper C. Austen Angell 《Journal of the American Ceramic Society》1983,66(9):c153-c154
A study of the high-alkali region of glass formation in the system Na2 O +B2 O3 reveals that retention of CO2 from carbonate starting materials can become a serious preparative problem at the high-alkali extreme. Results presented for glasses prepared using both Na2 O and Na2 CO3 show that residual CO2 can lead to major differences in physical properties which in this work are represented by the viscosity-related glass transition temperature . 相似文献
16.
Fine-particle beta sodium ferrite (β-NaFeO2 ), rather than α-Fe2 O3 , may be responsible for superparamagnetic behavior in a glass of composition (in mole fractions) 0.37Na2 O-0.26Fe2 O3 -0.37SiO2 . The 700°C isothermal section of the phase diagram of the Na2 O-Fe2 O3 -SiO2 system is given, showing a three-phase field bounded by Na2 SiO3 -NaFeO2 -Fe2 O3 ; there is no evidence for the existence (at 700°C) of compounds of molar composition 6Na2 O-4Fe2 O3 -5SiO2 or 2Na2 O-Fe2 O3 -SiO2 . The Moessbauer spectrum of β-NaFeO2 has an internal magnetic field of 487 kOe at room temperature. 相似文献
17.
Yaping Zhang Yunxia Yang Yuwen Ou Wei Hua Jiahua Zheng Guorong Chen 《Journal of the American Ceramic Society》2009,92(8):1881-1883
Glasses with compositions 50Bi2 O3 – x Sb2 O3 –10B2 O3 –(40– x ) SiO2 ( x =0, 1, 3, 5, 8, 10) have been prepared by conventional melt quench technique. Substitution of Sb2 O3 for SiO2 exerted an obvious effect on properties of glasses, especially, increased glass transition temperature ( T g ) and crystalline temperature ( T c ) greatly. Results of infrared transmission spectra attributed the effect to the formation of new bridging bonds of Sb–O–B and Sb–O–Si in glass network. 相似文献
18.
S. JILL GLASS PATRICK S. NICHOLSON C. BURTON CLARK A. H. HEUER 《Journal of the American Ceramic Society》1985,68(7):176-C
The interfacial reaction between Y2 O3 -partially-stabilized ZrO2 and α-Al2 O3 was studied. It was noted that α-Al2 O3 forms inside the periphery of the β-Al2 O3 grains; its formation suggests the loss of Na2 O from the p-Al2 O3 , either by evaporation or by dissolution in the ZrO2 matrix. The presence of Na2 ZrO3 is suspected. 相似文献
19.
Chung-Kook Lee Yolande Berta Robert F. Speyer 《Journal of the American Ceramic Society》1996,79(1):183-192
A glass crystallization method was utilized to synthesize nanosized BaO-6Fe2 O3 platelets from a 0.412BaO-0.258B2 O3 -0.330Fe2 O3 batch composition. Quenched ribbons were inhomogeneous, showing microclustering and ∼1 μm hematite crystals. Na2 O substitutions for BaO greatly enhanced the glass-forming tendency of quenched ribbons, though quenched-in ∼0.5 μm barium ferrite crystals were infrequently present. The improved homogeneity with Na2 O substitution was attributed to lower vapor pressure of BaO during batch melting, which increased its retention in the as-quenched ribbons. Quantities of BaO equal to or in excess of Fe2 O3 allowed iron ions to adopt stable network positions in the glass melt. With Na2 O substitution, devitrification of dispersed ∼40 nm barium ferrite particles from phase-separated regions occurred after secondary heat treatment. 5 mol% Na2 O batch substitution showed the lowest crystallinity in the as-quenched ribbons, and the highest crystallinity after secondary heat treatment. After optimum devitrification, the maximum values of saturation magnetization and coercivity were 21.22 emu/g and 2.82 kOe, respectively. 相似文献
20.
E. F. RIEBLING 《Journal of the American Ceramic Society》1973,56(6):303-309
Binary Sb2 O3 -GeO2 glasses containing 45 mol% Sb2 O3 and ternary Sb2 O3 -B2 O3 -GeO2 glasses containing 50 mol% GeO2 were prepared. Their densities (volumes), refractive indices, and infrared spectra were determined, and their colors and high-temperature viscosities were estimated visually. Small amounts of Sb2 O3 (∼10 mol%) appear to perturb neither the Ge-O-Ge network nor those B-O-Ge networks with small B/Ge ratios (∼0.2). The B-O-Ge networks with larger B/Ge ratios (∼1.0) depolymerize in the presence of even less Sb2 O3 . Amounts of Sb2 O3 >10 mol% appear to depolymerize the Ge-O-Ge and Ge-O-B networks progressively, possibly with the formation of chains. A structurally sensitive ir isofrequency contour technique developed for ternary glass systems was applied successfully to these Sb2 O3 -B2 O3 -GeO2 glasses. These contours can thus readily detect significant network depolymerization in the absence of the usual network modifiers. 相似文献