Abstract

Abstract Ten Cu(II)-polyimine complexes were tested as potential catalysts in oxygen delignification of softwood kraft pulps. The ligands were chosen from the terpyridine and the phenanthroline families, including several neocuproines. One diamine-phenanthrene (daphen) was also investigated. The main purpose was to examine whether the presence of methyl or phenyl substituents would direct the oxidation toward lignin. As a catalyst for comparison, unsubstituted 1,10-phenanthroline was selected, which is known to activate both delignification and carbohydrate degradation during oxygen bleaching of kraft pulp. The variation of ligands was aiming at the complex solubility and redox potential of the parameters. The experiments were performed on a mixture of mechanical pulp and fully bleached kraft pulps, a fully bleached pulp alone, and an industrial unbleached pulp. Concerning the oxygen activation in delignification of kraft pulp, 4,7-diphenyl-1,10-phenanthroline was as good as 1,10-phenanthroline, but appeared to be more selective, which resulted in a higher DPv of cellulose after treatment. This was interpreted by the structural similarities between the ligand and the kraft lignin and by a better stability of the intermediate complex with lignin. Two Cu(II)-phenanthroline derivatives complexes (4,7- and 5,6-dimethyl-1,10-phenanthroline) were also identified as effective oxygen activators for the removal of native lignin.

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