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Silver Ions Drive Ordered Self-Assembly Mechanisms and Inherent Properties of Lignin Nanoflowers

Designing anisotropic lignin-based particles and promoting the high-value utilization of lignin have nowadays drawn much attention from scientists. However, systematic studies addressing the self-assembly mechanisms of anisotropic lignin-based particles are scarce. In this work, an interaction inclu...

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Detalles Bibliográficos
Autores principales: Chen, Kai, Liu, Encheng, Yuan, Shengrong, Zhang, Baoquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10489698/
https://www.ncbi.nlm.nih.gov/pubmed/37688167
http://dx.doi.org/10.3390/polym15173541
Descripción
Sumario:Designing anisotropic lignin-based particles and promoting the high-value utilization of lignin have nowadays drawn much attention from scientists. However, systematic studies addressing the self-assembly mechanisms of anisotropic lignin-based particles are scarce. In this work, an interaction including the electrostatic forces and chelating forces between lignin and Ag(+) was regulated via carboxymethylation modification. Subsequently, the aggregation morphology of carboxymethylated lignin in a Ag(+) solution was observed via SEM. The result showed that a large number of Ag(+) intercalated into the lignin molecules when the grafting degree of the carboxyl groups increased from 0.17 mmol/g to 0.53 mmol/g, which caused the lignin molecules to gradually transform from disordered blocks to ordered layers. Dynamics research indicated that the adsorption process of Ag(+) in carboxymethylated lignin conforms to the Pseudo-first-order kinetic model. The saturated adsorption amount of Ag(+) in the carboxymethylated lignin reached 1981.7 mg/g when the grafting rate of carboxyl groups increased to 0.53 mmol/g, which then fully intercalated into lignin molecules and formed a layered structure. The thermodynamic parameters showed that the thermal adsorption process conforms to the Langmuir model, which indicates that Ag(+) is monolayer-adsorbed and intercalated into lignin molecules. Meanwhile, the ΔH values are more than 0, which suggests that this adsorption process is a endothermic reaction and that a higher temperature is conducive to an adsorption reaction. Therefore, self-assembly of lignin in a Ag(+) solution under 70 °C is more conducive to the formation of a nanoflower structure, which is consistent with our experimental result. Finally, pH-responsive Pickering emulsions were successfully prepared using a lignin-based nanoflowers, which demonstrated their potential as a catalytic platform in the interface catalysis field. This work offers a deeper understanding into the formation mechanism of anisotropic lignin-based nanoflowers and hopes to be helpful for designing and preparing anisotropic lignin-based particles.