Zhang Aiping, Lu Fachuang, Liu Chuanfu, Sun Run-Cang
State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640, China.
J Agric Food Chem. 2010 Nov 10;58(21):11287-93. doi: 10.1021/jf103354x. Epub 2010 Oct 18.
A three-step sequential extraction-precipitation method was used to isolate lignin from Eucalyptus tereticornis. The ball-milled eucalyptus was extracted with 96% dioxane, 50% dioxane, and 80% dioxane containing 1% NaOH at boiling temperature, consecutively resulting in solubilization of lignin and hemicelluloses. By precipitating such solutions into 70% aqueous ethanol, the hemicelluloses were removed substantially although there were still some carbohydrates left over, especially for lignin fraction extracted by 50% dioxane. Lignins dissolved in the 70% ethanol solutions were recovered via concentration and precipitation into acidified water. About 37% of the original lignin was released following such procedure whereas only 13.5% can be isolated by traditional milled wood lignin (MWL) method. The obtained lignin fractions were analyzed by high performance anion exchange chromatography (HPAEC) following acid hydrolysis for sugar composition of the contaminating carbohydrates and characterized by quantitative (31)P NMR as well as two-dimensional heteronuclear single-quantum coherence ((13)C-(1)H) NMR. The results showed that 96% aqueous dioxane extraction of ball-milled wood under conditions used in this study resulted in lignin preparation with very similar structures and sugar composition as traditional MWL. Therefore extracting ball-milled wood with 96% aqueous dioxane produced lignin in 33.6% yield, which makes it very attractive as an alternative to the traditional MWL method. However further extraction with 50% aqueous dioxane or 80% aqueous dioxane containing 1% NaOH gave just a little more lignins with different carbohydrate compositions from those in MWL. The eucalyptus lignins obtained were syringyl and guaiacyl type units. Lignin fraction obtained from 96% dioxane extraction was found to have more phenolic hydroxyl and less aliphatic hydroxyl than the other two preparations.
采用三步连续萃取-沉淀法从粗皮桉中分离木质素。将球磨后的桉木依次用96%二氧六环、50%二氧六环和含1%氢氧化钠的80%二氧六环在沸腾温度下萃取,从而使木质素和半纤维素溶解。将这些溶液沉淀到70%乙醇水溶液中,虽然仍有一些碳水化合物残留,但半纤维素基本上被除去,特别是对于用50%二氧六环萃取的木质素部分。溶解在70%乙醇溶液中的木质素通过浓缩并沉淀到酸化水中进行回收。经过此步骤后,约37%的原始木质素被释放出来,而采用传统磨木木素(MWL)法只能分离出13.5%。对获得的木质素部分进行酸水解后,通过高效阴离子交换色谱(HPAEC)分析其中污染碳水化合物的糖组成,并通过定量(31)P核磁共振以及二维异核单量子相干((13)C-(1)H)核磁共振进行表征。结果表明,在本研究使用的条件下,对球磨木材进行96%二氧六环水溶液萃取得到的木质素制剂,其结构和糖组成与传统MWL非常相似。因此,用96%二氧六环水溶液萃取球磨木材,木质素产率为33.6%,这使其作为传统MWL法的替代方法非常有吸引力。然而,进一步用50%二氧六环水溶液或含1%氢氧化钠的80%二氧六环水溶液萃取,得到的木质素仅比MWL中的多一点,且碳水化合物组成不同。所获得的粗皮桉木质素为紫丁香基和愈创木基型单元。发现从96%二氧六环萃取得到的木质素部分比其他两种制剂具有更多的酚羟基和更少的脂肪族羟基。