Ball-milled and enzyme lignins were produced from abaca fibre via ball mill
ing for 6 days followed by cellulase treatment for 3 days. The crude lignin
preparations were fractionated into milled lignin (ML), enzyme lignin (EL)
, hemicellulose-rich milled lignin (HRML), and Lignin-rich enzyme lignin (L
REL) fractions using a two-step precipitation method instead of a tradition
al ether precipitation procedure. The yield and chemical composition of the
resulting lignin samples are reported. The ME and EL fractions contained l
ow amounts of associated neutral sugars (2.0-3.3%) and uronic acids (1.4-1.
5%), and showed relatively low average molecular weights (2500-2660), while
the LREL and HRML fractions contained large amounts of bound polysaccharid
es (35.6-38.3%), and showed high molecular weights (8800-25000). The four l
ignin fractions are composed of a large proportion of syringyl units with f
ewer guaiacyl and p-hydroxyphenyl units. The ML is mainly composed of beta-
O-4 ether bonds between the lignin structural units. The less common beta-b
eta, beta-5 and 5-5' carbon-carbon linkages are also present in the lignin
molecules. It was found that uronic acids and 41-63% of p-coumaric acids ar
e esterified to lignin in the three lignin-rich fractions of ML, EL and LRE
L. This level increased to over 90% in the hemicellulose-rich fraction of H
RML. For ferulic acids, 92-97% were found to be etherified to Lignin in the
three lignin-rich fractions of ML, EL and LREL, while in the hemicellulose
-rich fraction of HRML this reduced to only 13%, suggesting that a majority
of the ferulic acids are esterified to hemicelluloses or lignin in this fr
action. (C) 1999 Society of Chemical Industry.