氨基酸基深共晶溶剂中木质素溶解行为的机理研究。
Mechanistic insights into the lignin dissolution behavior in amino acid based deep eutectic solvents.
机构信息
Faculty of Chemical and Energy Engineering, Universiti Teknologi Malaysia (UTM), 81310 Johor Bahru, Malaysia; Pollution Prevention Biotechnology Laboratory of Hebei Province, School of Environmental Science and Engineering, Hebei University of Science and Technology, Shijiazhuang, Hebei 050018, China.
Pollution Prevention Biotechnology Laboratory of Hebei Province, School of Environmental Science and Engineering, Hebei University of Science and Technology, Shijiazhuang, Hebei 050018, China.
出版信息
Int J Biol Macromol. 2023 Jul 1;242(Pt 2):124829. doi: 10.1016/j.ijbiomac.2023.124829. Epub 2023 May 19.
Deep eutectic solvents (DESs) composed by amino acids (L-arginine, L-proline, L-alanine) as the hydrogen bond acceptors (HBAs) and carboxylic acids (formic acid, acetic acid, lactic acid, levulinic acid) as hydrogen bond donors (HBDs) were prepared and used for the dissolution of dealkaline lignin (DAL). The mechanism of lignin dissolution in DESs was explored at molecular level by combining the analysis of Kamlet-Taft (K-T) solvatochromic parameters, FTIR spectrum and density functional theory (DFT) calculations of DESs. Firstly, it was found that the formation of new hydrogen bonds between lignin and DESs mainly drove the dissolution of lignin, which were accompanied by the erosion of hydrogen bond networks in both lignin and DESs. The nature of hydrogen bond network within DESs was fundamentally determined by the type and number of functional groups in both HBA and HBD, which affected its ability to form hydrogen bond with lignin. One hydroxyl group and carboxyl group in HBDs provided active protons, which facilitated proton-catalyzed cleavage of β-O-4, thus enhancing the dissolution of DESs. The superfluous functional group resulted in more extensive and stronger hydrogen bond network in the DESs, thus decreasing the lignin dissolving ability. Moreover, it was found that lignin solubility had a closed positive correlation with the subtraction value of α and β (net hydrogen donating ability) of DESs. Among all the investigated DESs, L-alanine/formic acid (1:3) with the strong hydrogen-bond donating ability (acidity), weak hydrogen-bond accepting ability (basicity) and small steric-hindrance effect showed the best lignin dissolving ability (23.99 wt%, 60 °C). On top of that, the value of α and β of L-proline/carboxylic acids DESs showed some positive correlation with the global electrostatic potential (ESP) maxima and minima of the corresponding DESs respectively, indicating the analysis of ESP quantitative distributions of DESs could be an effective tool for DESs screening and design for lignin dissolution as well as other applications.
由氨基酸(L-精氨酸、L-脯氨酸、L-丙氨酸)作为氢键受体(HBAs)和羧酸(甲酸、乙酸、乳酸、乙酰丙酸)作为氢键供体(HBDs)组成的深共晶溶剂(DESs)被制备并用于溶解脱碱木质素(DAL)。通过结合分析 Kamlet-Taft(K-T)溶剂化参数、DESs 的傅里叶变换红外光谱(FTIR)和密度泛函理论(DFT)计算,从分子水平上探讨了木质素在 DESs 中的溶解机制。首先,发现木质素与 DESs 之间形成新的氢键主要驱动了木质素的溶解,这伴随着木质素和 DESs 中氢键网络的侵蚀。DESs 内氢键网络的性质本质上取决于 HBA 和 HBD 中官能团的类型和数量,这影响了其与木质素形成氢键的能力。HBDs 中的一个羟基和一个羧基提供了活性质子,这促进了质子催化的β-O-4 的断裂,从而增强了 DESs 的溶解能力。HBDs 中多余的官能团导致 DESs 中更广泛和更强的氢键网络,从而降低了木质素的溶解能力。此外,还发现木质素的溶解度与 DESs 的α和β(净供氢能力)的差值呈密切正相关。在所研究的所有 DESs 中,具有强氢键供体能力(酸性)、弱氢键受体能力(碱性)和小空间位阻效应的 L-丙氨酸/羧酸(1:3)表现出最好的木质素溶解能力(23.99wt%,60°C)。此外,L-脯氨酸/羧酸 DESs 的α和β值与相应 DESs 的全局静电势(ESP)最大值和最小值呈正相关,表明 DESs 的 ESP 定量分布分析可以成为一种有效的工具用于筛选和设计用于木质素溶解以及其他应用的 DESs。