0
Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Food & Water Policy & Risk Remediation Sign in to save

A layer-by-layer assembled superhydrophobic composite aerogel for rapid and high-capacity removal of microplastics from beverages

Materials Horizons 2025 4 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Qiyue Zhao, Qiyue Zhao, Xiaohua Jiang, Erdun Bao, Hongman Hou, Gongliang Zhang, Jingran Bi

Summary

A superhydrophobic composite aerogel was synthesized using a layer-by-layer strategy combining an "egg-box" cellulose nanofiber network with silicone polymers, achieving an impressive polystyrene microplastic adsorption capacity of 555.5 mg/g within 100 minutes—driven primarily by hydrophobic interactions—and demonstrating high stability and reusability for microplastic removal from beverages.

Polymers

The hierarchical integration of porous materials with rigid frameworks and biopolymer components enhances their adsorption performance. While combining porous substances with cellulose nanofibers (CNFs) to create high-performance hybrid aerogels holds significant potential, achieving this remains challenging due to suboptimal interfacial bonding and insufficient structural reinforcement from CNFs. In this study, a superhydrophobic composite aerogel (AGU6-(OH)2@PMSQ) was synthesized using a sequential bottom-up and layer-by-layer in situ growth strategy based on a robust dual-network structure formed by the "egg-box structure" and CNFs. The hierarchical porosity and superhydrophobicity of AGU6-(OH)2@PMSQ provided excellent adsorption capacity and sensitivity for polystyrene microplastics (PSM). The adsorption kinetics revealed that the adsorption capacity for PSM reached an impressive 555.556 mg g-1 within a short timeframe of 100 min. D-R model analysis indicated that hydrophobic interactions were the primary driving force behind the adsorption of PSM by AGU6-(OH)2@PMSQ. Meanwhile, simulation calculations confirmed that hydrogen bonding and C-H⋯π interactions also contribute to the adsorption process. Furthermore, AGU6-(OH)2@PMSQ demonstrated exceptional adsorption stability, reproducibility, and a high PSM removal rate in aqueous matrices. This innovative research offers a new insight for contaminant control in complex matrix environments.

Share this paper