期刊
HOLZFORSCHUNG
卷 69, 期 6, 页码 807-814出版社
WALTER DE GRUYTER GMBH
DOI: 10.1515/hf-2014-0281
关键词
H-1 NMR of lignin; P-31 NMR of lignin; Indulin AT kraft lignin; internal standard for NMR; lignosulfonate; milled wood lignin (MWL); quantification of hydroxyl groups
资金
- FLIPPRdegrees project
P-31 nuclear magnetic resonance (NMR) based on the derivatization reagent 2-chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane is a common approach for the hydroxyl group determination of lignins, but the results are sometimes less reproducible compared to other methods. In the present work, common pitfalls in P-31 NMR analysis of kraft lignin (KL) and lignosulfonates (LS) are addressed and the results are compared to those obtained by H-1 NMR spectroscopy. Several experimental parameters are revisited in terms of the reliability of the obtained data, such as the choice of relaxation delay, internal standards, and the best solution technique for the P-31 NMR analysis of LS. For the first time, P-31 NMR data of LS are presented based on a new dissolution protocol. The analytical data of a set of lignins consisting of three KLs, one LS, and one milled wood lignin are presented based on the optimized P-31 NMR approach.
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