Kim Seung-Yeon, Jeong Jin-Woo, Kim A-Jin, Lee Young-Ran, Lee Hye Sun, Lee Kangwon, Kim Seong-Joong
Bio-Convergence R&D Division, Korea Institute of Ceramic Engineering and Technology (KICET), 202 Osongsaengmyeong 1-ro, Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do, Republic of Korea; Department of Applied Bioengineering, Seoul National University, 145 Gwanggyo-ro, Yeongtong-gu, Suwon-si, Gyeonggi-do, Republic of Korea.
Bio-Convergence R&D Division, Korea Institute of Ceramic Engineering and Technology (KICET), 202 Osongsaengmyeong 1-ro, Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do, Republic of Korea.
J Colloid Interface Sci. 2025 Jul 15;690:137304. doi: 10.1016/j.jcis.2025.137304. Epub 2025 Mar 11.
Size-controllable droplets were formed in a water in oil (W/O) emulsion using only hydrophilic polymers without a surfactant to fabricate porous micro-silica particles larger than 20 μm. Droplets of various size ranging from 1 to 30 μm were prepared by emulsifying aqueous solutions containing four types of polymers, namely polyethylene glycol (PEG), polyvinyl alcohol (PVA), polyvinylpyrrolidone (PVP), and polypropylene glycol (PPG), in a pentanol oil phase. Following the addition of tetraethyl orthosilicate (TEOS) as a silica precursor, silica particles were grown via hydrolysis and condensation reactions. The silica particle size depends on the degree of hydrophilicity of the polymers, which determines the interfacial tension between the water droplets and oil. Micro-silica particles >20 μm were obtained from PEG-based emulsion droplets. Notably, the distribution and stability of silica particles can be optimized by controlling the molecular weight and concentration of the hydrophilic polymer. A porous silica structure was successfully obtained by decomposing the residual polymer via an appropriate calcination process. The most uniform and stable porous micro-silica particles with an average size of 20 μm were obtained from an emulsion containing 5 wt% PEG (molecular weight: 4000) after calcination at 500 °C. This novel process enables the eco-friendly synthesis of porous micro-silica particles using only hydrophilic polymer without a surfactant and control of pore size and particle size of >20 μm.
仅使用亲水性聚合物而非表面活性剂,在油包水(W/O)乳液中形成尺寸可控的液滴,以制备大于20μm的多孔微二氧化硅颗粒。通过在戊醇油相中乳化含有四种聚合物(即聚乙二醇(PEG)、聚乙烯醇(PVA)、聚乙烯吡咯烷酮(PVP)和聚丙二醇(PPG))的水溶液,制备了尺寸范围从1至30μm的各种液滴。添加原硅酸四乙酯(TEOS)作为二氧化硅前驱体后,通过水解和缩合反应使二氧化硅颗粒生长。二氧化硅颗粒的尺寸取决于聚合物的亲水性程度,亲水性决定了水滴与油之间的界面张力。从基于PEG的乳液液滴中获得了大于20μm的微二氧化硅颗粒。值得注意的是,通过控制亲水性聚合物的分子量和浓度,可以优化二氧化硅颗粒的分布和稳定性。通过适当的煅烧过程分解残留聚合物,成功获得了多孔二氧化硅结构。在500°C煅烧后,从含有5wt% PEG(分子量:4000)的乳液中获得了平均尺寸为20μm的最均匀、最稳定的多孔微二氧化硅颗粒。这种新工艺能够仅使用亲水性聚合物而非表面活性剂,实现对孔径大于20μm的多孔微二氧化硅颗粒的环保合成以及对其粒径的控制。