共 40 条
Analysis of lignocellulose derived phenolic monomers by headspace solid-phase microextraction and gas chromatography
被引:10
作者:
Kolb, Michaela
[1
]
Schieder, Doris
[1
]
Faulstich, Martin
[1
]
Sieber, Volker
[1
]
机构:
[1] Tech Univ Munich, D-94315 Straubing, Germany
关键词:
Gas chromatography;
Headspace;
Solid-phase microextraction;
Phenols;
Lignocellulose;
Lignin;
WHEAT-STRAW;
MASS-SPECTROMETRY;
GC-MS;
DEGRADATION-PRODUCTS;
ENZYMATIC-HYDROLYSIS;
ETHANOL-PRODUCTION;
SUGARCANE BAGASSE;
WET OXIDATION;
HS-SPME;
LIGNIN;
D O I:
10.1016/j.chroma.2013.07.094
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
A headspace solid-phase microextraction method with subsequent GC-MS (HS-SPME/GC-MS) was established for the quantitative analysis of volatile lignin derived phenolic monomers in complex aqueous solutions. Extraction was done using a polyacrylate fiber. The optimization of HS-SPME - parameters was performed using a multi component model solution of six representative phenolic monomers identified in liquid hot water (LHW) supernatants of hydrothermally treated lignocellulosic biomass: p-coumaric acid, guaiacol, vanillin, acetosyringone, 4-hydroxy-3-methoxyphenylacetone, and acetophenone. Plackett-Burman design was applied for pre-evaluation and 2(3) central composite designs with star points for parameter optimization. LOQ(S/N > 10) and LOD (S/N > 3) were determined for 12 phenols yielding LOQ of <0.005-618 nM and LOD of <0.005-412 nM. Within-day and between-day tests (n = 6) showed different results for the tested phenols. RSD ranged from 2% to 30% and recovery rates from 99% to 160% in LHW matrix. Tests on storage of LHW supernatants for several weeks indicated a considerable influence of temperature on the stability of the solutions which may even have to be taken into account for auto sampler handling. All in all the method allows a fast and solvent free analysis requiring low sample volumes making it a powerful tool for screening or high-throughput analysis of aqueous solutions of lignin derived aromatics. (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:144 / 157
页数:14
相关论文