From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins”

化学 木质素 过氧化氢 摩尔质量 溶剂 溶解度 摩尔比 有机化学 聚合物 催化作用
作者
Gerhild K. Wurzer,Markus Bacher,Oliver Musl,Nadine Kohlhuber,Irina Sulaeva,Theres Kelz,Karin Fackler,Robert H. Bischof,Hubert Hettegger,Antje Potthast,Thomas Rosenau
出处
期刊:RSC Advances [The Royal Society of Chemistry]
卷期号:13 (14): 9479-9490 被引量:2
标识
DOI:10.1039/d3ra00691c
摘要

A new chemical modification protocol to generate N-lignins is presented, based on Indulin AT and Mg2+-lignosulfonate. The already known ammonoxidation reaction in liquid phase was used as a starting point and stepwise optimised towards a full solid-state approach. The "classical" liquid ammonoxidation products, the transition products from the optimization trials, as well as the "solid-state" products were comprehensively analysed and compared to the literature. The N-lignins obtained with the conventional ammonoxidation protocol showed the same properties as reported. Their molar mass distributions and the hydroxy group contents, hitherto not accessible due to solubility problems, were measured according to a recently reported protocol. N-Indulin showed an N-content up to 11 wt% and N-lignosulfonate up to 16 wt%. The transition experiments from liquid to solid-state gave insights into the influence of chemical components and reaction conditions. The use of a single chemical, the urea-hydrogen peroxide complex (UHP, "carbamide peroxide"), was sufficient to generate N-lignins with satisfying N-content. This chemical acts both as an N-source and as the oxidant. Following the optimization, a series of solid-state ammonoxidation tests were carried out. High N-contents of 10% in the case of Indulin and 11% in the case of lignosulfonate were obtained. By varying the ratio of UHP to lignin, the N-content can be controlled. Structural analysis showed that the N is organically bound to the lignin, similar to the "classical" ammonoxidation products obtained under homogeneous conditions. Overall, a new ammonoxidation protocol was developed which does not require an external gas supply nor liquids or dissolved reactants. This opens the possibility for carrying out the lignin modification in closed continuous reactor systems, such as extruders. The new, facile solid-state protocol will hopefully help N-lignins to find more consideration as a fertilizing material and in soil-improving materials.

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