Startseite Anthraquinone polymer catalysts for alkaline delignification of lignocellulosic matter. Part 2. Action in soda pulping conditions on softwood and phenolic β-O-4 lignin models
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Anthraquinone polymer catalysts for alkaline delignification of lignocellulosic matter. Part 2. Action in soda pulping conditions on softwood and phenolic β-O-4 lignin models

  • Emmanuel Cazeils , Jackson D. Megiatto , Christian Gardrat , Frédérique Pichavant , Stéphane Grelier und Alain Castellan EMAIL logo
Veröffentlicht/Copyright: 16. Juni 2012
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Abstract

Two hydrophobic and one hydrophilic anthraquinone (AQ) polystyrene catalysts were tested under soda pulping conditions on thermomechanical fibers, and the results were evaluated based on commercial AQ. Hydrophobic and hydrophilic polymers had efficiency gains of 23%–28% and 57%, respectively, compared to AQ (100% efficiency). Hydrosolubility of AQ polymers played a major role in delignification efficiency, a property that allows a better contact with lignocellulosic fibers. Hydrophobic copolymers were stable under pulping conditions and preserved their catalytic effect entirely by contrast to the hydrophilic AQ, as demonstrated by recovery yields after pulping and catalytic action of the recovered copolymers. Studies on lignin models confirmed that the hydrophilic AQ polystyrene is a better catalyst under soda pulping conditions than the hydrophobic ones. It was demonstrated that AQ polystyrene polymers react with lignin models by electron transfer mechanisms.


Corresponding author.Laboratoire de Chimie des Polymères Organiques, UMR 5629 Université Bordeaux 1/CNRS, ENSCBP/IPB, Bâtiment A, 16 Avenue Pey-Berland, F-33607 Pessac, France Phone: +33-5-4000-6280Fax: +33-5-4000-8487

Received: 2011-12-14
Accepted: 2012-5-2
Published Online: 2012-06-16
Published in Print: 2012-08-01

©2012 by Walter de Gruyter Berlin Boston

Artikel in diesem Heft

  1. Masthead
  2. Masthead
  3. Original Papers
  4. Anthraquinone polymer catalysts for alkaline delignification of lignocellulosic matter. Part 1. Syntheses and characterizations
  5. Anthraquinone polymer catalysts for alkaline delignification of lignocellulosic matter. Part 2. Action in soda pulping conditions on softwood and phenolic β-O-4 lignin models
  6. Anthraquinone polymer catalysts for alkaline delignification of lignocellulosic matter. Part 3. Delignification of softwood and action on a phenolic β-O-4 lignin model in kraft pulping conditions
  7. Analysis of fibre deformation processes in high-consistency refining based on Raman microscopy and X-ray diffraction
  8. Distribution of wood polymers within the cell wall of transgenic aspen imaged by Raman microscopy
  9. Chemical improvement of surfaces. Part 2: Permanent hydrophobization of wood by covalently bonded fluoroorganyl substituents
  10. Testing of the superhydrophobicity of a zinc oxide nanorod array coating on wood surface prepared by hydrothermal treatment
  11. Properties of molding plates made with albizia wood particles impregnated with alcohol-soluble PF resins prepared from phenol-liquefied lignins
  12. Within-ring movement of free water in dehydrating Norway spruce sapwood visualized by neutron radiography
  13. Influence of hygromechanical history on the longitudinal mechanosorptive creep of wood
  14. Effects of systematic variation of wood adherend bending stiffness on fracture properties: Part 1. Influence of grain angle
  15. Effects of systematic variation of wood adherend bending stiffness on fracture properties. Part 2. Revisiting traditional DCB analysis methods
  16. Determination of adhesive energy at the wood cell-wall/UF interface by nanoindentation (NI)
  17. Short Notes
  18. Distribution of extracts including 4,8-dihydroxy-5-methoxy-2-naphthaldehyde in Diospyros kaki analyzed by gas chromatography-mass spectrometry and time-of-flight secondary ion mass spectrometry
  19. Southern pine impregnated with silicate solution containing cellulose nanofibrils
  20. Meetings
  21. Meetings
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