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Novel intermediate temperature solid oxide fuel cell based on La-doped Bi4V2O11 electrolyte 基于la掺杂Bi4V2O11电解质的新型中温固体氧化物燃料电池
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-05-18 DOI: 10.1080/17436753.2021.1927443
G. Paściak, J. Chmielowiec
ABSTRACT The electrolyte supported intermediate temperature solid oxide fuel cell (IT-SOFC) based on Bi4V2O11 (BIVOX) ceramic stabilised by doping with La was investigated. By adding La to the initial composition of BIVOX, stabilisation of the good oxygen ion-conductive γ phase has been achieved. La addition has significantly increased the lifetime of SOFC due to the improved thermodynamic stability of BIVOX electrolyte in reducing (H2 – fuel) atmosphere. Such fuel cell parameters as: open circuit voltage (OCV), maximum power density (P) and current density (J) in the temperature range 500–800°C and operating time under constant electronic load were determined. Results of the measurements of these electrical parameters for BILAVOX based single cell in function of the operation time and cyclic load changes were also shown. This is the first report on the construction and electrical properties of fuel cells based on BIMEVOX (BIVOX doped with MEtal) ceramics.
研究了掺杂La稳定的Bi4V2O11 (BIVOX)陶瓷电解质负载的中温固体氧化物燃料电池(IT-SOFC)。通过在BIVOX的初始组成中加入La,实现了良好氧离子导电性γ相的稳定。La的加入提高了BIVOX电解质在还原(H2 -燃料)气氛中的热力学稳定性,从而显著提高了SOFC的寿命。测定了燃料电池在500 ~ 800℃温度范围内的开路电压(OCV)、最大功率密度(P)和电流密度(J)以及恒定电子负载下的工作时间等参数。本文还给出了基于BILAVOX的单电池的这些电参数随运行时间和循环负荷变化的测量结果。这是基于BIMEVOX (BIVOX掺杂金属)陶瓷的燃料电池的结构和电性能的第一篇报道。
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引用次数: 2
Athermal electric field effects in flash sintered zirconia 闪烧氧化锆中的非热电场效应
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-05-03 DOI: 10.1080/17436753.2021.1919361
Jian Dong, M. Biesuz, V. Sglavo, M. Kermani, Xiaojia Su, T. Saunders, Chunfeng Hu, S. Grasso
ABSTRACT We propose an innovative methodology to quantify the dependence of grain growth with respect to current density during flash sintering of zirconia (3YSZ) (field set under a nominal current limit of 150 mA mm−2. This was achieved by using a notch (0.5 mm deep and 1.5 mm wide) located in the middle of a dog-bone specimen, allowing an uneven current distribution (ranging from 3 to 670 mA mm−2) while maintaining a fairly homogeneous temperature (1420–1500 °C). Microstructure observations nearby the notch tip confirmed localised overheating. The modelling approach decoupled thermal and electrical field effects identifying the long questioned athermal electric field effects in flash sintering. Increased current density seems to weakly restrain grain growth, to accelerate densification, to promote defects healing (i.e. notch, cracks and pores) and inter-particle bond formation. These results could rationalise the athermal effects occurring during FS and flash joining.
我们提出了一种创新的方法来量化氧化锆(3YSZ)闪烧过程中晶粒生长与电流密度的依赖关系(场设置在标称电流限制150 mA mm−2下)。这是通过使用位于狗骨标本中间的缺口(0.5 mm深,1.5 mm宽)来实现的,允许不均匀的电流分布(范围从3到670 mA mm−2),同时保持相当均匀的温度(1420-1500°C)。缺口尖端附近的显微组织观察证实了局部过热。该建模方法解耦了热电场效应,确定了闪烧过程中长期存在的非热电场效应。电流密度的增加似乎对晶粒生长有微弱的抑制作用,加速致密化,促进缺陷愈合(即缺口、裂纹和孔隙)和颗粒间键的形成。这些结果可以合理地解释FS和闪蒸连接过程中出现的非热效应。
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引用次数: 5
Influence of the sintering method on densification, microstructure and electrical conductivity of 12Ce-TZP 烧结方式对12Ce-TZP致密化、显微组织和电导率的影响
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-05-03 DOI: 10.1080/17436753.2021.1919362
L. S. Ferreira, E. Muccillo
ABSTRACT Zirconia containing 12 mol-% cerium oxide ceramics were prepared by solid state reaction utilising the conventional, fast firing and two-step sintering methods. The sintering temperature and time were varied aiming to determine ideal sintering profile for these methods. The monoclinic and tetragonal phase contents, microstructure and electrical conductivity of dense specimens were investigated. The linear shrinkage was found negligible up to 1100°C and the maximum rate of shrinkage was achieved at 1150°C. Densification increased up to 2 h for conventional sintered specimens. Stabilisation of tetragonal phase in non-isothermally sintered specimens occurred at a high temperature (1500°C). Specimens sintered by the two-step method attained high density along with small grain sizes. Optimised sintering profiles were determined for all the sintering methods used.
摘要采用常规、快速烧成和两步烧结法,采用固相反应法制备了含12mol %氧化铈的氧化锆陶瓷。改变烧结温度和烧结时间,以确定这些方法的理想烧结曲线。研究了致密试样的单斜相和四方相含量、显微组织和电导率。线形收缩率在1100℃以下可以忽略不计,在1150℃达到最大收缩率。常规烧结试样致密化时间延长至2 h。在高温(1500℃)下,非等温烧结试样中的四方相发生稳定。两步法烧结的试样密度高,晶粒尺寸小。确定了所有烧结方法的最佳烧结轮廓。
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引用次数: 1
Thermally stable piezoelectric performance in low-temperature sintered Pb0.95Ba0.01Sr0.04(Zr0.53Ti0.47)O3 ceramics with a low loss factor 低温烧结Pb0.95Ba0.01Sr0.04(Zr0.53Ti0.47)O3低损耗陶瓷的热稳定压电性能
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-04-28 DOI: 10.1080/17436753.2021.1919363
Zongzheng Du, Yi-Xuan Liu, Wenqing Wei, Hong Liu, Shengqi Jiang, Jingzhong Fang
ABSTRACT Herein, Pb0.95Ba0.01Sr0.04(Zr0.53Ti0.47)O3 piezoelectric ceramics comprising 0.25 wt% MnCO3, 1 wt% LiBiO2 and 0.06 wt% CuO (PBSZT-LBCu-Mn ceramics, abbreviated as Mn0.25) were prepared via a conventional method at a low firing temperature of ∼900 °C. The phase structure and temperature-dependent electrical properties were systematically investigated. The product composition possesses the following properties: normalised strain (d 33*) ∼362 pm/V, Curie temperature (T c) ∼336 °C, mechanical quality factor (Q m) ∼568, loss factor (tan δ) ∼0.0058 and relative dielectric constant (ϵ r) ∼872. The remnant polarisation (P r), maximum polarisation (P max) and coercive field (E c) slightly decreased as a function of increasing temperature, while the strain (S pol) was observed to increase. Additionally, d 33* values of 362 and 411 pm/V were achieved at 25 °C and 120 °C, respectively, with a change ratio <14%. The Mn0.25 ceramics exhibit low ϵ r and tan δ values, leading to small average power dissipation, which is beneficial for high-frequency actuator applications.
本文采用常规方法,在~ 900℃的低温下制备了Pb0.95Ba0.01Sr0.04(Zr0.53Ti0.47)O3压电陶瓷(含0.25 wt% MnCO3, 1 wt% LiBiO2和0.06 wt% CuO) (PBSZT-LBCu-Mn陶瓷,简称Mn0.25)。系统地研究了其相结构和随温度变化的电学特性。产品组成具有以下特性:归一化应变(d 33*) ~ 362 pm/V,居里温度(T c) ~ 336°c,机械品质因子(Q m) ~ 568,损耗因子(tan δ) ~ 0.0058,相对介电常数(λ) ~ 872。残余极化(P r)、最大极化(P max)和矫顽力场(E c)随温度的升高而减小,而应变(S pol)随温度的升高而增大。在25°C和120°C时,d 33*值分别为362和411 pm/V,变化率<14%。Mn0.25陶瓷具有较低的λ和tan δ值,平均功耗小,有利于高频执行器的应用。
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引用次数: 1
Highly flexible and strong SiC fibre mats prepared by electrospinning and hot-drawing 采用静电纺丝和热轧法制备高柔韧性、高强度的碳化硅纤维垫
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-04-03 DOI: 10.1080/17436753.2021.1904767
Pengpeng Yu, Zijia Lin, Y. Mu, Jie Yu
ABSTRACT Silicon carbide (SiC) fibres are widely used as promising reinforcement in ceramic matrix composites due to their excellent mechanical and thermal properties. In this work, sub-micrometer SiC fibres were prepared by electrospinning using polycarbosilane as the precursor, followed by curing in air and pyrolysing at high temperatures. The effect of the microstructure of SiC fibres on mechanical properties was investigated and the SiC fibre mats prepared at 1300°C for 2 h exhibited a mechanical strength of 184.5 ± 19.4 MPa. Hot-drawing was conducted on as-spun fibres during the curing process and the strength, Young’s modulus, and flexibility of SiC fibre mats were improved. The strength with a drawing ratio of 200% reaches 243.0 ± 17.5 MPa. The enhancement of mechanical strength after hot-drawing is mainly attributed to the reduced defects in fibres, improvement in the orientation of the precursor fibres as well as the alignment of the molecular chains in the precursor fibres.
碳化硅纤维由于其优异的力学性能和热学性能,在陶瓷基复合材料中得到了广泛的应用。本文以聚碳硅烷为前驱体,采用静电纺丝法制备了亚微米SiC纤维,然后在空气中固化,在高温下热解。研究了SiC纤维的微观结构对力学性能的影响,在1300℃下保温2 h制备的SiC纤维垫的机械强度为184.5±19.4 MPa。在固化过程中对未纺纤维进行热拉伸,提高了SiC纤维垫的强度、杨氏模量和柔韧性。拉伸率为200%时强度达到243.0±17.5 MPa。热拉伸后机械强度的提高主要是由于纤维缺陷的减少、前驱体纤维取向的改善以及前驱体纤维分子链的排列。
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引用次数: 2
Effects of Fe2O3 on crystallisation and properties of R2O–CaO–MgO–Al2O3–SiO2–Fe2O3 glass ceramics Fe2O3对r20 - cao - mgo - al2o3 - sio2 - Fe2O3玻璃陶瓷结晶及性能的影响
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-04-03 DOI: 10.1080/17436753.2021.1911583
Jiawei Zhong, J. Xue, Yong-Qiu Huang
ABSTRACT The R2O–CaO–MgO–Al2O3–SiO2–Fe2O3 glass ceramics was prepared using granite wastes and Fe2O3. The effect of Fe2O3 on crystallisation and properties of glass ceramics was studied. Results show that the crystalline phases were Fe2TiO5 and K(NaCa)Mg5Si8O22F2 when the content of Fe2O3 was low. The main crystalline phase was Fe1.5Ti0.5O3 when the content of Fe2O3 was high. With the increase of Fe2O3, the crystal size of K(NaCa)Mg5Si8O22F2 reduced and the atomic ratio of Si to Mg increased. The colour of sample varied from greyish green to black with different additions of Fe2O3. The flexural strength with a maxim (101.02 MPa) when the content of Fe2O3 was 4.7 mol-%. Given the low cost of granite wastes and Fe2O3, this new type of black glass ceramics is expected to meet the increasing demand from the market of building decoration due to its excellent properties.
以花岗岩废料和Fe2O3为原料制备了r20 - cao - mgo - al2o3 - sio2 - Fe2O3玻璃陶瓷。研究了Fe2O3对玻璃陶瓷结晶和性能的影响。结果表明:当Fe2O3含量较低时,晶相为Fe2TiO5和K(NaCa)Mg5Si8O22F2;当Fe2O3含量较高时,主要晶相为Fe1.5Ti0.5O3。随着Fe2O3含量的增加,K(NaCa)Mg5Si8O22F2晶粒尺寸减小,Si / Mg原子比增大。Fe2O3添加量不同,样品的颜色由灰绿色到黑色不等。当Fe2O3含量为4.7 mol-%时,材料的抗弯强度最大(101.02 MPa)。鉴于花岗岩废料和Fe2O3成本低廉,这种新型黑色玻璃陶瓷以其优异的性能有望满足建筑装饰市场日益增长的需求。
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引用次数: 3
Paste backward extrusion process as a suitable method for fabrication of sodium beta-alumina electrolyte closed-end tubes 浆料反向挤压法是制备β -氧化铝钠电解质封端管的合适方法
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-04-03 DOI: 10.1080/17436753.2021.1911582
H. A. Moghadam, M. H. Paydar
ABSTRACT In this study, paste backward extrusion is introduced for fabrication of sodium beta-alumina electrolyte closed-end tubes (with a wall thickness of 1 mm and external diameter of 8.0 mm). For this purpose, the two-piece extrusion die was designed and extrudable water-based paste was prepared by using sodium beta-alumina powder, polyvinyl pyrrolidone, as a binder, and ethylene glycol as a plasticizer. The effect of solvent content on the rheological parameters of the paste and the ram extrusion velocity on the liquid phase separation are investigated. The results indicate that the optimum solvent content for making the extrudable paste is in the range of 30–35 wt-%, and the liquid phase separation is obviously occurred when the ram velocity is lower than 1.2 mm s−1. It was also shown that by using backward extrusion, and by applying optimum conditions, closed-end tubes with high density (about 97%) and good surface quality could be fabricated successfully.
本研究采用浆料反向挤压法制备了β -氧化铝钠电解质封端管(壁厚为1mm,外径为8.0 mm)。为此,设计了两片式挤出模具,以-氧化铝钠粉、聚乙烯醇吡咯烷酮为粘结剂,乙二醇为增塑剂,制备了可挤出的水基糊状物。考察了溶剂含量对膏体流变参数的影响,以及柱塞挤压速度对液相分离的影响。结果表明,制备可挤出糊状物的最佳溶剂含量为30 ~ 35 wt-%,当滑块速度小于1.2 mm s - 1时,会发生明显的液相分离。结果表明,采用反向挤压工艺,在适当的条件下,可以成功制备出高密度(约97%)、表面质量良好的封端管。
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引用次数: 1
Aesthetic restoration of anterior teeth with different coloured substrates using digital monolithic zirconia crowns: two case reports 采用数字单片氧化锆冠对不同颜色基板的前牙进行美观修复:2例报告
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-04-03 DOI: 10.1080/17436753.2021.1915086
Zhe Sun, Lifang Wu, Jing Zhao, Yuanna Zheng
ABSTRACT Tooth discolouration and the existence of metallic substrates increase the difficulty of restoration to reproduce natural and aesthetic appearance. The commonly used veneered zirconia restorations have a high risk of porcelain chipping, and the monolithic zirconia restorations cannot always achieve satisfying aesthetics. The newly developed self-glazed monolithic zirconia restorations digitally manufactured by additive technique have colour- and translucency-gradient characteristics. They could mask the different coloured substrates and achieve a natural look simultaneously. This clinical report describes the prosthodontic treatments of two patients with different coloured substrates in the anterior region. Both functional and aesthetic outcomes are satisfactory after 1–3 years of follow-up.
牙齿变色和金属基质的存在增加了修复再现自然美观外观的难度。常用的贴面氧化锆修复体存在瓷片脱落的风险,整体氧化锆修复体往往不能达到令人满意的美观效果。新开发的自上釉单片氧化锆修复体具有彩色和半透明梯度特性。他们可以掩盖不同颜色的基材,同时获得自然的外观。本临床报告描述了两名患者在前区不同颜色基底的修复治疗。经过1-3年的随访,功能和美学结果均令人满意。
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引用次数: 3
Catalytic performance of porous Yb2O3 sesquioxide 多孔Yb2O3倍半氧化物的催化性能
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-04-03 DOI: 10.1080/17436753.2021.1919359
Alina Aftab, Katerina L. Chagoya, Alan Felix, R. Blair, N. Orlovskaya
ABSTRACT Porous Yb2O3 ceramic (55%) was pressureless sintered at 900°C for four hours in air. The crystal structure of Yb2O3 was confirmed to be cubic ( ) with c = 10.43731 Å by neutron diffraction. The spectral vibrational signature of Yb2O3 was also confirmed by micro-Raman spectroscopy. Yb2O3 is an amphoteric oxide with both acid and base character, which presents the potential for producing different hydrocarbons when used as a Fischer–Tropsch (FT) catalyst. It was found that Yb2O3 is indeed catalytically active and can be used to convert syngas (CO + H2) into useful hydrocarbons. Production of methane, ethene, and ethane was detected in the catalytic experiment performed at 500°C, but propane, propene, butane, and methanol were also detected in the experiment performed at 250°C. Hydrocarbons heavier than C4 were not observed. The limited data show deviation from a Flory–Schulz distribution suggesting additional surface processes are occurring beyond chain growth and termination.
将多孔Yb2O3陶瓷(55%)在900℃的空气中无压烧结4小时。通过中子衍射证实Yb2O3的晶体结构为立方(),c = 10.43731 Å。微拉曼光谱也证实了Yb2O3的光谱振动特征。Yb2O3是一种兼有酸碱性质的两性氧化物,当用作费托催化剂时,有可能产生不同的碳氢化合物。发现Yb2O3确实具有催化活性,可以将合成气(CO + H2)转化为有用的碳氢化合物。在500°C的催化实验中检测到甲烷、乙烯和乙烷的产生,但在250°C的实验中也检测到丙烷、丙烯、丁烷和甲醇。没有观察到比C4重的碳氢化合物。有限的数据显示与Flory-Schulz分布的偏差,表明在链生长和终止之外还发生了其他表面过程。
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引用次数: 0
Electron redistribution and acid site of tungsten-doped CeTiOx with oxygen vacancies 含氧空位的钨掺杂CeTiOx的电子重分布和酸位
IF 2.2 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS Pub Date : 2021-04-03 DOI: 10.1080/17436753.2021.1919360
Myung-Kun Kim, G. Park, Min-Chul Shin, Hong-Dae Kim, Dae-Seung Cho, Heesoo Lee
ABSTRACT The enhancement of surface acidity for tungsten-doped CeTiOx was investigated through electronic structure. Tungsten doping increased the ratio of Ce3+ from 12.0% to 29.6%, which was confirmed by XPS. The doped tungsten was present as W5+ in a ratio of 71.5%. In O K-edge XAS spectra, increase in indicated the formation of oxygen vacancies through tungsten doping. The decrease in W 5d-eg peak intensity demonstrated the occupation of the W 5d orbital by electrons formed at the oxygen vacancies. The enrichment of W5+ was owing to transfer of electrons to 5d-eg orbital of tungsten rather than to cerium ions. The acid sites were analysed using FTIR and NH3-TPD. The peak intensity of Brønsted acid sites and amount of NH3 desorption increased from 66.2 to 136.1 µmol g−1 with tungsten doping. The doped tungsten formed Brønsted acid sites and led to enhanced surface acidity and catalytic activity.
通过电子结构研究了钨掺杂CeTiOx表面酸度的增强。钨的掺杂使Ce3+的比例从12.0%提高到29.6%,XPS证实了这一点。掺杂后的钨以W5+的形式存在,比例为71.5%。在O - k边缘XAS光谱中,增加表明钨掺杂形成了氧空位。w5d -eg峰强度的降低表明在氧空位上形成的电子占据了w5d轨道。W5+的富集是由于电子转移到钨的5d-eg轨道而不是转移到铈离子。用FTIR和NH3-TPD分析了酸位。钨掺杂后,Brønsted酸位的峰值强度和NH3解吸量从66.2µmol g−1增加到136.1µmol g−1。掺杂的钨形成了Brønsted酸位,提高了表面酸度和催化活性。
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引用次数: 1
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