ISSN 1008-5548

CN 37-1316/TU

最新出版

超声空化协同聚乙二醇诱导制备球形二氧化硅

Preparation of spherical silica induced by ultrasonic cavitation and polyethylene plycol


彭小丰a, 邓金明a, 李福枝b, 廖海洋c, 石 璞a

湖南工业大学 a. 包装工程学院, b. 材料科学与工程学院, c. 机械工程学院, 湖南 株洲 412007


引用格式:

彭小丰, 邓金明, 李福枝, 等. 超声空化协同聚乙二醇诱导制备球形二氧化硅[J]. 中国粉体技术, 2026, 32(4): 1-9.

Peng Xiaofeng, Deng Jinming, Li Fuzhi, et al. Preparation of spherical silica induced by ultrasonic cavitation and polyethylene plycol[J]. China Powder Science and Technology, 2026, 32(4): 1-9.

DOI:10.13732/j.issn.1008-5548.2026.04.015

收稿日期:2025-09-27, 修回日期: 2026-03-17,上线日期: 2026-05-19。

基金项目:国家自然科学基金项目,编号:22209020。

第一作者简介:彭小丰(2003—),男,硕士生,研究方向为二氧化硅功能材料。E-mail:2247653173@qq.com。

通信作者简介:石璞(1976—),男,副教授,硕士,硕士生导师,研究方向为高分子材料与新型能源材料。E-mail:shipu1976@163.com。


摘要:【目的】开发一种基于廉价硅酸钠(Na2SiO3)的低成本、绿色合成工艺,用以制备高性能二氧化硅(SiO₂)微球,旨在替代依赖正硅酸乙酯(tetraethyl orthosilicate,TEOS)的传统方法。【方法】采用超声空化协同聚乙二醇(polyethylene glycol,PEG)诱导的种子生长法,以廉价Na2SiO3为硅源,通过优化PEG含量、超声功率和陈化时间等关键参数,实现对SiO2微球形貌、粒径及分散性的精准调控;并利用傅里叶红外光谱仪、扫描电镜和激光粒度仪观察优化制备的SiO2微球的结构与形貌。【结果】超声波功率为500 W、PEG 2000添加量为2 g、陈化时间为4 h时效果最佳,制备出的SiO2微球球形度优、分散性好,中值粒径为3.6 μm。【结论】该方法突破传统TEOS工艺的成本与环保限制,为低成本绿色制备高性能SiO2微球提供新策略。

关键词:硅酸钠;二氧化硅微球;超声空化

Abstract

Objective SiO2 microspheres have broad application prospects in pharmaceuticals, coatings, cosmetics, optoelectronics, and industrial catalysis due to their advantages such as high hardness, high packing density, good flowability, and low abrasion. However, traditional preparation methods mainly rely on tetraethyl orthosilicate (TEOS) as the silicon source, which presents problems such as high cost, low silicon content, and the use of large amounts of organic solvents during the reaction process. These limitations hinder large‑scale application and are inconsistent with the principles of green chemistry. Therefore, this study aims to develop a low-cost and green synthesis process based on inexpensive Na2SiO3 to replace the TEOS-based method, achieving sustainable production of high‑performance SiO2 microspheres. By optimizing key parameters, the issues of poor morphology and easy agglomeration of microspheres prepared with Na2SiO3 as the silicon source are addressed, offering a feasible solution for industrial application.

Methods An ultrasonic cavitation‑assisted, polyethylene glycol (PEG)‑induced seed growth method was employed, using low‑cost Na2SiO3 as the silicon source, to systematically optimize process parameters such as PEG content, ultrasonic treatment, and aging time. The structure, morphology, and particle size of the SiO2 microspheres were characterized using Fourier‑transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and laser particle size analysis. Additionally, zeta potential analysis was combined to evaluate the stability of the particle dispersion system. The effects of PEG content, ultrasonic treatment, and aging time on the morphology, particle size, and dispersibility of microspheres were investigated.

Results and Discussion As a morphology‑directing agent, PEG not only effectively stabilized the precursor and particle surfaces through hydrogen bonding, but also provided steric hindrance effects. The synergistic effects of both stabilized the reaction system. The ultrasonic cavitation effect generated local high‑pressure zones and micro‑jets, which disrupted weak inter‑particle interactions and prevented agglomeration. The aging process followed the Ostwald ripening mechanism, promoting a more uniform particle size distribution. When the aging time reached 4 h, the absolute zeta potential value reached ‑51 mV, at which point the electrostatic repulsion between SiO2 microspheres was strongest, effectively suppressing agglomeration.

Conclusion This study successfully develops a green synthesis process based on ultrasonic cavitation combined with PEG‑induced seeding, using inexpensive Na2SiO3 to replace TEOS to prepare high‑performance SiO2 microspheres. The optimal process parameters are ultrasonic power of 500 W, PEG2000 dosage of 2 g, and aging time of 4 h. The obtained microspheres exhibit excellent sphericity, good dispersibility, and a median particle size of 3.6 μm. Through synergistic optimization of multiple parameters, this method overcomes the limitations of high cost and poor environmental friendliness of traditional processes, providing a low‑cost, scalable preparation strategy for SiO2 microspheres in fields such as pharmaceuticals and coatings. Future research can explore the regulation of microsphere pore size and the extension of their applications in porous materials.

Keywords: sodium silicate; silica microspheres; ultrasonic cavitation


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