Jf. Kadla et al., REACTIONS OF LIGNIN WITH CYANAMIDE ACTIVATED HYDROGEN-PEROXIDE PART 1- THE DEGRADATION OF LIGNIN MODEL COMPOUNDS, Holzforschung, 52(5), 1998, pp. 506-512
Monomeric lignin model compounds representing various functional group
s found in residual lignins were reacted with cyanamide activated hydr
ogen peroxide. Non-phenolic lignin model compounds failed to react eve
n under extreme reaction conditions (90 degrees C), while phenolic lig
nin model compounds underwent rapid oxidation. Reaction optimization s
tudies reveal that these reactions are strongly dependent on pH and th
e cyanamide-to-peroxide ratio, while temperature is not a factor. Thro
ugh the use of electron paramagnetic resonance (EPR) spectroscopy free
radical involvement has been demonstrated. Ln contrast to previous li
terature, a predominately free-radical mechanism exists, and on the ba
sis of the reactions carried out in the presence of superoxide dismuta
se, the presence of . O-2(-) has been determined.