石油炼制与化工 ›› 2026, Vol. 57 ›› Issue (2): 146-157.

• 研究报告 • 上一篇    下一篇

金属封装型silicalite-1分子筛的制备及其对丙酮吸附性能的研究

骆龙华1,汤思瑶1,董鹏2,李铁森1,2,崔勍焱1,岳源源1,2   

  1. 1. 福州大学化工学院
    2. 清源创新实验室
  • 收稿日期:2025-09-02 修回日期:2025-10-21 出版日期:2026-02-12 发布日期:2026-01-27
  • 通讯作者: 岳源源 E-mail:yueyy@fzu.edu.cn
  • 基金资助:
    国家自然科学基金项目;国家自然科学基金项目;清源创新实验室贵重仪器设备开放测试基金;清源创新实验室贵重仪器设备开放测试基金;清源创新实验室贵重仪器设备开放测试基金

PREPARATION OF METAL-ENCAPSULATED SILICALITE-1 ZEOLITE AND ITS ADSORPTION PERFORMANCE FOR ACETONE

  • Received:2025-09-02 Revised:2025-10-21 Online:2026-02-12 Published:2026-01-27

摘要: 常规silicalite-1 (S-1)分子筛因酸位点数量有限,难以高效吸附极性的挥发性有机化合物分子(如丙酮)。基于此,利用原位合成法向S-1分子筛中引入金属Ag,Cu,Fe,Ni,制备了一系列金属封装型S-1分子筛,并对S-1及金属封装型S-1分子筛进行了系统表征和丙酮吸附性能测试。结果表明:Fe@S-1对丙酮的吸附性能最佳,Fe@S-1上丙酮的吸附穿透容量较S-1提升了约10%,这归因于Fe的引入显著提高了S-1的微孔比表面积和Lewis酸位点数量;随着Fe添加量增加,Fe@S-1的Lewis酸位点数量呈上升趋势,样品晶粒逐渐减小,并堆积形成具有晶间介孔的聚集态颗粒。这些特性不仅增强了Fe@S-1对丙酮的吸附作用,而且降低了丙酮的扩散阻力,进而提高其对丙酮的吸附容量。吸附动力学模型拟合结果表明,丙酮在Fe@S-1上的吸附行为是物理吸附和化学吸附共同作用的结果,且孔道内扩散在吸附过程中占主导地位。

关键词: S-1分子筛, 金属封装, Lewis酸位点, 丙酮, 吸附, 挥发性有机化合物

Abstract: Conventional silicalite-1 (S-1) zeolite exhibits limited efficiency in adsorbing polar volatile organic compounds molecules (e.g., acetone) due to its scarcity of acid sites. Based on this, a series of metal-encapsulated S-1 zeolites were prepared by introducing metals Ag, Cu, Fe, and Ni into S-1 via in-situ synthesis. Systematic characterization and acetone adsorption performance tests were conducted on both S-1 and the metal-encapsulated S-1 zeolites. The results show that Fe@S-1 exhibits the best acetone adsorption performance, with its acetone adsorption breakthrough capacity increasing by approximately 10% compared to that of S-1. This improvement is attributed to the introduction of Fe, which significantly enhances the microporous specific surface area and the number of Lewis acid sites in S-1. As the Fe loading increases, the number of Lewis acid sites in Fe@S-1 shows an upward trend, and the crystal grains gradually decrease in size, forming aggregated particles with intercrystalline mesopores. These characteristics not only enhance the adsorption of acetone on Fe@S-1 but also reduce the diffusion resistance of acetone, thereby improving its adsorption capacity for acetone. The fitting results of the adsorption kinetic model indicate that the adsorption behavior of acetone on Fe@S-1 is governed by both physisorption and chemisorption, with intraparticle diffusion playing a dominant role in the adsorption process.

Key words: S-1 zeolite, metal encapsulating, Lewis acid site, acetone, adsorption, volatile organic compounds