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  • 1
    Publication Date: 2006-07-01
    Description: The utilization of western red cedar mechanical pulp is limited by low brightness caused by a high chromophore content. In this paper we identify these chromophores and provide a possible mechanism for their formation during the mechanical pulping process. Diffuse reflectance ultraviolet (DRUV) and Fourier-transform infrared (DRIFT) spectra were recorded for western red cedar chemimechanical pulp treated with hydrogen peroxide, sodium borohydride and acetic anhydride. Treatment with hydrogen peroxide was conducted over different time periods. The spectra indicate that three carbonyl-containing chromophores contribute to light absorption in the visible region. Two conjugated ortho-quinones contributed most of the color. These quinones were formed by oxidation and polymerization of lignans during the refining process. The third chromophore was coniferaldehyde. There was a large initial time lag for the reaction of peroxide with coniferaldehyde relative to reaction time with the quinones. We ascribe this to differences in topochemistry. It was deduced that coniferaldehyde was mainly associated with lignin in the interior of the fiber wall, whereas the quinones were derived from lignans that had been deposited on the fiber surface. Identification of the three chromophores provides a basis for studies of the kinetics of brightening of western red cedar mechanical pulps.
    Print ISSN: 0018-3830
    Electronic ISSN: 1437-434X
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Published by De Gruyter
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  • 2
    Publication Date: 2000-04-13
    Description: Summary Three quarters of the western red cedar's heartwood colour is due to a polymeric material easily isolated by methanol extraction. The nature of this polymer has not been fully investigated and published information is contradictory. Our initial examination of the coloured polymer by pyrolysis-gas chromatography, combined with mass spectrometry, indicated that the polymer was guaiacyl in nature and thus similar to softwood lignin. However, analysis by infrared spectroscopy indicated the presence of both lignin and lignan like moieties. To clarify this issue a more detailed analysis was conducted using nuclear magnetic resonance spectroscopy (1H NMR, 31P NMR, 13C NMR). Analysis of the spectra and comparison with the spectra of plicatic acid and a product from mild acid treatment of plicatic acid, indicated that the polymeric fraction was derived almost entirely from lignans. During polymer formation, the highly reactive pyrocatechol moiety in the plicatic acid is destroyed, leaving a guaiacyl-like polymer. The reaction mechanism appears to proceed via an ortho-quinone intermediate followed by polymerization.
    Print ISSN: 0018-3830
    Electronic ISSN: 1437-434X
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Published by De Gruyter
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
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