硅酸盐学报

凝胶反应速率对Y₂O₃坯体微观结构及透明陶瓷制备的影响

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杨亮 ¹ , 李晓东 ¹ , 穆浩洁 ¹ , 史树君 ² , 徐维富 ² , 孙旭东 ¹

硅酸盐学报 | 研究论文 2025,53(9): 2664-2674

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硅酸盐学报 |研究论文 2025 , 53 (9) : 2664 -2674

凝胶反应速率对Y₂O₃坯体微观结构及透明陶瓷制备的影响

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杨亮¹, 李晓东¹, 穆浩洁¹, 史树君², 徐维富², 孙旭东¹

作者信息

^1．东北大学材料科学与工程学院，材料各向异性与织构教育部重点实验室，沈阳 110819

^2．深圳市德镒盟新材料有限公司，广东深圳 518038

通讯作者:

李晓东（1971—），男，博士，教授。

作者简介:

杨亮（2001—），男，硕士研究生。

Influence of Gelation Rate on Microstructure of Green Bodies and Preparation of Y₂O₃ Transparent Ceramics

Liang YANG¹, Xiaodong LI¹, Haojie MU¹, Shujun SHI², Weifu XU², Xudong SUN¹

Affiliations

^1.School of Materials Science and Engineering, Northeastern University, Key Laboratory of Material Anisotropy and Texture, Ministry of Education, Northeastern University, Shenyang 110819, Guangdong, China

^2.Shenzhen DEM Technology Co., Ltd. Shenzhen 518038, Guangdong, China

Corresponding Author:

LI Xiaodong (1971-), male, Ph.D., Professor. E-mail: xdli@mail.neu.edu.cn

YANG Liang (2001-), male, Master Candidate. E-mail: liangyang0222@163.com

出版时间: 2025-09-20 doi: 10.14062/j.issn.0454-5648.20250178

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摘要

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Y₂O₃透明陶瓷以其卓越的透光性和低发射率特性，在固体激光器、透明窗口材料及高温结构部件等领域展现出广阔的应用潜力。随着Y₂O₃透明陶瓷应用领域的持续扩展，传统的干压成型方法在满足陶瓷尺寸和形状多样性需求方面存在局限性。凝胶注模成型技术在大尺寸、复杂形状陶瓷零部件的制备上具有显著优势，但干燥开裂和微观结构不均匀一直是影响陶瓷零部件良品率的关键因素。针对丙烯酰胺凝胶注模体系中的坯体微观结构不均匀问题，深入研究凝胶反应速率的精确控制。实验设计了8组不同条件，包括催化剂加入量［0.02%（质量分数）、0.04%、0.08%、0.12%］和凝胶反应温度（25、40、60、80 ℃），以探讨凝胶反应速率对成型坯体微观结构均匀性的影响。研究表明，当催化剂加入量为0.04%、反应温度控制在60 ℃时，既能确保浆料的充分充型，又能获得完整且微观结构均匀的陶瓷样品。通过精确调控凝胶反应速率，成功构建了均匀的凝胶网络，进而实现了Y₂O₃坯体的微观结构均匀化。最终，采用1850 ℃真空烧结6 h工艺制备出的Y₂O₃透明陶瓷（厚度为2 mm）在800 nm波长处的透过率高达82%。

关键词

氧化钇 / 透明陶瓷 / 凝胶注模 / 微观结构变化 / 真空烧结

Abstract

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Introduction

Y₂O₃ transparent ceramics are increasingly demanded in advanced technological applications, particularly in high-power laser systems, infrared optical windows, and semiconductor devices. These applications require materials that maintain both exceptional optical transmittance (i.e., >80% at 1064 nm) and mechanical strength (i.e., flexural strength >200 MPa), even when fabricated into complex geometries. Gel casting offers a promising route for producing large-scale, complex-shaped Y₂O₃ components. However, process-induced defects such as delamination, microcracks, and density gradients often compromise the microstructural integrity of green bodies, leading to a reduced performance in the ceramics. These defects primarily stem from excessive internal stresses generated during gelation, thus highlighting a need for precise control over gelation kinetics. This study was to investigate the synergistic effects of catalyst concentration and reaction temperature on the microstructural homogeneity of Y₂O₃ green bodies. The highly uniform green bodies were obtained via optimizing the parameters, thus enabling the fabrication of Y₂O₃ transparent ceramics with a high optical performance through vacuum sintering.

Methods

A certain amount of commercial Y₂O₃ powder was mixed with ethanol as a dispersion medium. The slurry was ground in a ball mill with ZrO₂ beads of 2 mm in diameter for 8 h. Ammoniumpolymethacrylate (A40) was added as a dispersant, concentrated H₂SO₄ as an additive and ZrO(NO₃)₂ as a sintering aid. The ground slurry was placed in an oven to dry at 120 ℃ for 6 h. After drying, the powder was sifted through a 200-mesh screen. The sifted powder was then calcined in air at a certain temperature for 4 h to obtain a Y₂O₃ nano-powder.

Acrylamide (AM) and N,N'-Methylenebisacrylamide (MBAM) were dissolved in deionized water to prepare a 15% AM aqueous solution in a mass ratio of AM to MBAM of 88∶10. After the organic compounds were completely dissolved, 5 mm ZrO₂ beads were added in a mass ratio of ball-to-powder of 5∶2. Tetramethylammonium Hydroxide (TMAH), ammonium citrate (TAC), A40, and Y₂O₃ powder were then added sequentially to prepare Y₂O₃ slurry with a solid content of 50%. The suspension was ground at 170 r/min for 6 h, then degassed under a vacuum of 1×10^-1Pa for 30 min. Catalyst and initiator were added sequentially, and followed via degassing the slurry again under a vacuum of 1×10^-1Pa for 3 min. Finally, the well-mixed slurry was poured into polytetrafluoroethylene or silicone molds heated at different temperatures (i.e., 25, 40, 60, and 80 ℃). The obtained green bodies were dried in air.

Results and discussion

The gelation rate is evaluated via monitoring temperature variations during the process. The results show that increasing catalyst content accelerates gelation, but exceeding 0.08% causes a rapid reaction, leading to a green body cracking. The SEM images reveal a stratified microstructure, with a dense surface layer and a porous interior. The dense layer thickness decreases as catalyst content increases. Elevated reaction temperature also enhances gelation rate, and, stratification disappears at 60 ℃, yielding uniformly porous structures.

The infrared spectra of green bodies (i.e., 0.02% catalyst, 25 ℃) indicate an incomplete AM polymerization on the surface, while a well-developed PAM network in the interior impeded particle movement during drying. This structural disparity results in a dense surface and porous interior.

Pre-sintered green bodies exhibit heterogeneous microstructures that persist during densification. Higher catalyst content and temperature reduce the surface dense layer thickness and internal porosity.

The final vacuum-sintered samples further demonstrate that lower gelation reaction temperatures correspond to thicker surface dense layers under identical vacuum sintering temperatures, significantly hindering the expulsion of internal pores in the ceramics. This results in the center of the ceramic exhibiting an opaque condition.

Conclusions

Y₂O₃ transparent ceramics with excellent properties were prepared via gel casting and vacuum sintering with Y₂O₃ nano-powder as a raw material. During the gel casting process, the rate of gelation significantly affected the uniformity of the green body microstructure. A complete and uniformly structured Y₂O₃ green body was obtained via controlling the factors influencing the gelation rate at a catalyst addition of 0.04% and a reaction temperature of 60 ℃, while ensuring that the slurry met the filling requirements. After vacuum sintering at 1850 ℃ for 6 h, the obtained Y₂O₃ transparent ceramic (with a thickness of 2 mm) achieved a transmittance of 82% at 800 nm. This study demonstrated that during the gel casting process, the rate of gelation could affect the uniformity of the internal microstructure of the green body, and this internal microstructural non-uniformity further influence the subsequent densification process of the ceramic during sintering.

Key words

yttria / transparent ceramic / gel casting / microstructure evolution / vacuum sintering

引用本文

杨亮, 李晓东, 穆浩洁, 史树君, 徐维富, 孙旭东. 凝胶反应速率对Y₂O₃坯体微观结构及透明陶瓷制备的影响. 硅酸盐学报, 2025 , 53 (9) : 2664 -2674 . DOI: 10.14062/j.issn.0454-5648.20250178

Liang YANG, Xiaodong LI, Haojie MU, Shujun SHI, Weifu XU, Xudong SUN. Influence of Gelation Rate on Microstructure of Green Bodies and Preparation of Y₂O₃ Transparent Ceramics[J]. Journal of the Chinese Ceramic Society, 2025 , 53 (9) : 2664 -2674 . DOI: 10.14062/j.issn.0454-5648.20250178

基金

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国家自然科学基金(52472065)

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2025年第53卷第9期

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文章信息

doi: 10.14062/j.issn.0454-5648.20250178

接收时间：2025-03-17
首发时间：2026-10-21
出版时间：2025-09-20

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收稿日期：2025-03-17
修回日期：2025-03-27

基金

国家自然科学基金(52472065)

作者信息

^1．东北大学材料科学与工程学院，材料各向异性与织构教育部重点实验室，沈阳 110819

^2．深圳市德镒盟新材料有限公司，广东深圳 518038

通讯作者:

李晓东（1971—），男，博士，教授。

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2种不同金属材料的力学参数

科 Family	属数 Number of genus	种数 Number of species	占总种数比例 Percentage of total species (%)	属 Genus	种数 Number of species	占总种数比例 Percentage of total species (%)
鹅膏菌科Amanitaceae	2	11	5.26	鹅膏菌属 Amanita	10	4.78
小菇科 Mycenaceae	2	12	5.74	丝盖伞属 Inocybe	5	2.39
多孔菌科 Polyporaceae	8	14	6.70	蜡蘑属 Laccaria	5	2.39
红菇科 Russulaceae	3	23	11.00	小皮伞属 Marasmius	6	2.87
				小菇属 Mycena	11	5.26
				光柄菇属 Pluteus	5	2.39
				红菇属 Russula	17	8.13
				栓菌属 Trametes	5	2.39

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