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热压2%(mol)Y2O3—ZrO2陶瓷中t—m相等温转变 总被引:2,自引:0,他引:2
用热膨胀分析、X射线衍射研究了热压2%(mol)Y2O3-ZrO2陶瓷中t-m等温转变动力学。结果表明:经过快速冷却而得到的四方相(t)在随后200~400℃区间保温时发生了四方相(t)到单斜相(m)的转变。该转变的时间-温度-转变量(TTT)曲线呈C形,鼻子温度为300℃)。高于或低于上述温度范围,未出现m相,可用Avrami方程的一般形式来描述动力学曲线。该相变的形核与长大均是时间的函数,相变 相似文献
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研究了ZrN在Si_3N_4-ZrO_2复相陶瓷中的形成及其对材料性能的影响,结果表明:在1.5MPaN2气压烧结条件下,ZrN的形成温度约为1600℃,提高N_2的压力有利于抑制ZrN的生成,以稳定的t-ZrO_2加Si_3N_4基体中,对抑制ZrN的生成有明显作用。当复相陶瓷中生成一定量的ZrN时,力学性能明显下降,而ZrO_2分布均匀且以t-ZrO_2,c-ZrO_2形式存在时,复相陶瓷具有较高的强度(740MPa)和断裂韧性(8.8MPa·m ̄(1/2))。 相似文献
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固定化细胞生产L-苹果酸新工艺及动力学研究 总被引:2,自引:0,他引:2
对产氨短杆菌MA-2固定化细胞在富马酸铵体系中转化生成L-苹果酸的优化工艺条件做了探讨,结果表明,富马酸铵浓度为1.8mol/L,pH7.0~8.0,反应温度为37℃时,L-苹果酸得率达200g/L左右。同时,对固定化细胞的动力学进行了研究,结果为:r(max)=58mmol/(L·h·g固定化湿细胞)),Km=6.25×1O ̄(-2)mol/L,P_m=1.56mol/L 相似文献
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氧化锆在电场下的相变 总被引:4,自引:0,他引:4
在200-400℃温度范围内,电场可以显著促进3%Y2O3-ZrO2中四方相氧化锆向单斜相的转变,而且其等温动力学曲线呈抛物线规律,这说明在氧化四方相向单斜相的转变过程中存在着明显的扩散篚现象。另外,近阳极而的相变量明显高于阴极面的相变量,这说明该相变过程与氧空位或缺陷簇的迁移过程密切相关。 相似文献
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等离子喷涂ZrO2/NiCoCrAlY梯度涂层中ZrO2组元的显微结构特征 总被引:3,自引:0,他引:3
Zro2/NiCoCrAlY梯度涂层中的8%Y2O3部分稳定ZrO2组元在等离子喷涂后的快速凝固和冷却过程,发生了c→t’非扩散型相变的c→t扩散型相变,以及少量的t→m相变。涂层中ZrO2主要由未转变的c相及转变产物t相和t’相组成,并存在少量的m相。 相似文献
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助烧剂Y2O3对ZrO2(Y—TZP)—Si3N4系统中ZrO2相组成的影响 总被引:1,自引:0,他引:1
本文研究了助烧剂Y2O3对GPSZrO2(3mol%Y-TZP)-Si3N4系统中ZrO2相结构的影响。研究结果表明:ZrO2(Y-TZP)-Si3N4系统中不添加Y2O3助烧剂,ZrO2相组成主要以m-ZrO2形式存在,并有少量氮稳定ZrO2;ZrO2(Y-TZP)-Si3N4系统中添加5wt%Y2O3助烧剂,ZrO2相组成为c-ZrO2、不能相变的过稳定t-ZrO2。 相似文献
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Properties of two high performance engineering thermoplastics, amorphous polyethersulfone (PES) and semicrystalline polyetheretherketone (PEEK), are discussed. Both resins can be processed by conventional techniques, compounded with high performance fibers, and have high service temperature (up to 300°C). Due to the amorphous character PES can be dissolved and spray coated into metals. 相似文献
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Photopyroelectric (PPE) spectroscopy is a nondestructive tool that is used to study the optical properties of the ceramics (ZnO + 0.4MnO(2) + 0.4Co(3)O(4) + xV(2)O(5)), x = 0-1 mol%. Wavelength of incident light, modulated at 10 Hz, was in the range of 300-800 nm. PPE spectrum with reference to the doping level and sintering temperature is discussed. Optical energy band-gap (E(g)) was 2.11 eV for 0.3 mol% V(2)O(5) at a sintering temperature of 1025 °C as determined from the plot (ρhυ)(2)versushυ. With a further increase in V(2)O(5), the value of E(g) was found to be 2.59 eV. Steepness factor 'σ(A)' and 'σ(B)', which characterize the slope of exponential optical absorption, is discussed with reference to the variation of E(g). XRD, SEM and EDAX are also used for characterization of the ceramic. For this ceramic, the maximum relative density and grain size was observed to be 91.8% and 9.5 μm, respectively. 相似文献
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采用固相合成法制备了(Ba(1-α)Srα)4.8(Sm0.7La0.3)8.8Ti18O54(α=0.1~0.5)系陶瓷,表征了该陶瓷的相组成和显微结构,测试了微波介电性能.结果表明:α=0.3时,(Ba(1-α)Srα)4.8(Sm0.7La0.3)8.8Ti18O54系陶瓷为单相的新钨青铜结构固溶体.α>0.3时,相继出现了第二相BaLa2Ti4O12和La0.66TiO2.993.随α的增加,(Ba(1-α)Srα)4.8(Sm0.7La0.3)8.8Ti18O54系陶瓷的相对介电常数(εr)先增大后有所波动,品质因数(Qf)先增大后减小,谐振频率温度系数(τf)单调减小.α=0.3时,在1 350℃烧结的陶瓷的微波介电性能最佳:εr=98.77,Qf=5184GHz,τf=10.9×10-6/℃,优于不掺杂的BaO-Sm2O3-TiO2陶瓷的. 相似文献
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This semicrystalline phase, originally named ‘calcium silicate hydrate(II)’ by Taylor (1950), has been studied with X-rays, electron optics, chemical investigation of silicate anion type, infrared spectra, and thermal methods. It is structurally related to jennite (C9S6H11) and probably also to the fibrous CSH of cement pastes, the three phases forming a sequence of decreasing crystallinity. The specimen studied had approximate composition C2SH3.2 after standing over saturated CaCλ2 at about 15°C. CSH(II) contains metasilicate chains and pyrosilicate groups and has a disordered layer structure. Much of the water can be lost reversibly without significant change in lattice parameters. 相似文献
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Summary In the present work we describe, the synthesis and characterization of a new gel obtained by crosslinking a cooligomer of butadiene-acrylic acid (BuAA), by reaction with acrylonitrile and acrylic acid. The purified product was characterized by FTIR, elemental analyses and scanning electronic microscopy. The thermal properties were studied and swelling indexes were determined in different solvents and at different pH values. The capacity of poly(butadiene-acrylic acid(g)acrylonitrile(g)acrylic acid) [gel A] to separate different organic substances, such as amino acids and colorants, was determined. 相似文献
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Hybrid films of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) were prepared with different molecular weights of poly(ethylene oxide) (PEO). The cross-linking reaction between PEO and PEDOT:PSS was performed at high temperature and confirmed by using differential scanning calorimeter (DSC), contact angle measurement, and solid-state 1H NMR. The effect of chemical reaction on the conductivity and morphology of these hybrid films was studied by using 4-point probe and atomic force microscope (AFM), respectively. As-spun PEO/PEDOT:PSS films have lower electric conductivity due to the addition of nonconductive PEO, and exhibits no molecular weight dependence on conductivity. After chemical cross-linking reaction at high temperature, only PEDOT:PSS films with lowest molecular weight PEO additives show enhanced conductivity with increasing reaction time. AFM result indicates that the heat-treated PEO/PEDOT:PSS hybrid films show grain-like morphology compared to ethylene glycol treated PEDOT:PSS films which shows continuous PEDOT domain. In the present work we demonstrate that the cross-linking reaction can be used to improve the wet stability of PEDOT:PSS nanofiber, showing good water resistance and excellent dimensional stability. 相似文献
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The addition of side groups to improve the photooxidative stability of polymers used in polymer-based light-emitting diodes (LEDs) is explored. Infrared spectroscopy and computational chemistry techniques are used to study the effects of chemical substitution of the reactive vinylene moiety in poly(phenylene vinylene) (PPV). The bond order of the vinylene group in small oligomers is calculated using semiempirical techniques to assess the improvement in stability toward oxidants such as singlet oxygen. We find that PPV dimers allow relative comparisons across a range of possible substitutions. Experimental results correlate well with these calculations. The addition of electron-withdrawing substituents, such as nitrile groups, to the vinylene moiety is found to be particularly effective in reducing the reactivity of alkoxy-substituted PPV toward singlet oxygen. The photooxidative stability of a poly(phenylene acetylene) (PPA) derivative is also studied. It appears that this family of polymers is more stable toward photooxidation than are its PPV analogs. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 2451–2458, 1998 相似文献
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Witold Brostow Kwan-Ho Seo Jong B. Beak Jeong C. Lim Kwan-Ho Seo 《Polymer Engineering and Science》1995,35(12):1016-1021
The miscibilities of poly(phenylene) sulfide/poly(phenylene sulfide sulfone) (PPS/PPSS) and poly(phenylene) sulfide/poly(phenylene sulfide ether) (PPS/PPSE) blends were invesigated in terms of shifts of glass transition temperatures Tg of pure PPS, PPSS, a dn PPSE. The crystallization kinetics of PPS/PPSS blends was also studied as a function of molar composition. The PPS/PPSS and PPS/PPSE blends are respectively partially and fully miscible. PPSE shows a plasticizing effect on PPS as does PPS on PPSS, which necessarily improves te processibility in the respective systems. We can control Tg and melting temperature Tm of PPS by varying amounts of PPSE in blends. The melt crystallization temperature Tmc of PPS/PPSE blends was higher than that of the PPSE homopolymer. Therefore, these blends require shorter cycle times in processing than pure PPSE. The overall rate of crystallization for PPS/PPSS blends follows the Avrami equation with an exponent ?2. The maximal rate of crystallization for PPS/PPSS blends occurs at a temperatre higher by 10°C than that for PPS, while the crystallization half time t1/2 is 4 times shorter. In the cold crystallization range, crystal growth rates increase and Avrami exponents decrease significantly as the temperature increases. 相似文献