Coroabă Adina, Apostol Irina, Dascălu Ioan Andrei, Bele Adrian, Marangoci Narcisa Laura, Doroftei Florica, Uritu Cristina Mariana, Spiridon Iuliana
"Petru Poni" Institute of Macromolecular Chemistry, Grigore Ghica Vodă 41 A, 700487 Iași, Romania.
Center of Advanced Research in Bionanoconjugates and Biopolymers, "Petru Poni" Institute of Macromolecular Chemistry, 700487 Iași, Romania.
Polymers (Basel). 2025 Apr 29;17(9):1221. doi: 10.3390/polym17091221.
In the present study, carbon structures from LignoBoost lignin were synthetized using HNO/HSO one-pot hydrothermal treatment, followed by a thermal treatment. The obtained compounds were characterized using different techniques, such as FTIR, DVS, DLS, XRD, fluorescence imaging and STEM. The formed LCMs presented graphitized structure with quasi-spherical shapes. All obtained materials presented negative values of zeta potential due to the charge from the hydroxyl and carboxyl groups, as confirmed by XPS analysis. All the data obtained sustained the heterogeneous composition of the lignin-based carbon materials, which arise from the complex structure of lignin. Fluorescence imaging demonstrated the potential of the materials as optical imaging agents.
在本研究中,采用硝酸/硫酸一锅水热法处理并随后进行热处理,合成了来自LignoBoost木质素的碳结构。使用傅里叶变换红外光谱(FTIR)、动态蒸汽吸附(DVS)、动态光散射(DLS)、X射线衍射(XRD)、荧光成像和扫描透射电子显微镜(STEM)等不同技术对所得化合物进行了表征。形成的木质素基碳材料(LCMs)呈现出具有准球形形状的石墨化结构。X射线光电子能谱(XPS)分析证实,由于羟基和羧基的电荷作用,所有获得的材料的ζ电位均为负值。获得的所有数据均支持木质素基碳材料的非均相组成,这源于木质素的复杂结构。荧光成像证明了这些材料作为光学成像剂的潜力。
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