Home Effect of pH on lignin analysis by Raman spectroscopy
Article
Licensed
Unlicensed Requires Authentication

Effect of pH on lignin analysis by Raman spectroscopy

  • Elina Warsta , Anni Lähdetie , Anna-Stiina Jääskeläinen and Tapani Vuorinen EMAIL logo
Published/Copyright: November 30, 2011
Become an author with De Gruyter Brill
Holzforschung
From the journal Volume 66 Issue 4

Abstract

Ultraviolet resonance Raman (UVRR) spectroscopy is a powerful tool for structural lignin analysis in situ: modification or isolation of lignin from biomass is not necessary. UVRR spectroscopy is equally applicable for samples with high lignin content and those with very low lignin content. Monomeric phenolic lignin model compounds and wood pulp samples have been studied at neutral and alkaline pH with UVRR spectroscopy. Concentration of guaiacol correlated well with the relative Raman band intensity, which indicates that lignin-containing solutions can be quantitatively measured with UVRR spectroscopy. A change in pH induced a recordable shift in the aromatic band position in the spectra, which was 25–35 cm-1 with phenolic model compounds without para substitution, 8–12 cm-1 with phenolic model compounds with para substitution, and about 2–7 cm-1 with pulp samples. No shift was detected with a non-phenolic model compound. Increasing the amount of phenolic hydroxyl groups increased the UVRR band shift in pulp samples. Additionally, increasing the pH enhanced the relative aromatic band intensity in the UVRR spectra in solution of the phenolic model compound. Accordingly, pH adjustment is relevant prior to any lignin analysis with Raman spectroscopy.


Corresponding author. Aalto University, Department of Forest Products Technology, P.O. Box 16300, FI-00076 Aalto, Espoo, Finland

Received: 2011-8-17
Accepted: 2011-11-1
Published Online: 2011-11-30
Published in Print: 2012-05-01

©2012 by Walter de Gruyter Berlin Boston

Articles in the same Issue

  1. Original Papers
  2. Synthesis of glucose esters from cellulose in ionic liquids
  3. A new soy flour-polyepoxide adhesive system for making interior plywood
  4. Hydrophobisation of mechanical pulp fibres with sodium dodecyl sulphate functionalised layered double hydroxide particles
  5. Effect of pH on lignin analysis by Raman spectroscopy
  6. Fractionation and characterization of lignin carbohydrate complexes (LCCs) of Eucalyptus globulus in residues left after MWL isolation. Part I: Analyses of hemicellulose-lignin fraction (HC-L)
  7. Surface and internal micro/ultrastructure of TMP fibres produced during high-intensity refining elucidate the development of pulp and paper properties
  8. Mechanoradical formation and its effects on birch kraft pulp during the preparation of nanofibrillated cellulose with Masuko refining
  9. Influence of specimen configuration on the measurement of the off-axis Young’s modulus of wood by vibration tests
  10. Effect of lignin and hemicelluloses on the tensile strength of micro-veneers determined at finite span and zero span
  11. Revisiting the neutral axis in wood beams
  12. Relationship between copper species in solution and leaching from alkaline copper quat (ACQ) treated wood
  13. Assessment of the early signs of decay of Populus deltoides wafers exposed to Trametes versicolor by near infrared spectroscopy
  14. Community analysis of preservative-treated southern pine (Pinus spp.) using terminal restriction fragment length polymorphism (T-RFLP) analysis. Part 1: Fungal field study
  15. Community analysis of preservative-treated southern pine (Pinus spp.) using terminal restriction fragment length polymorphism (T-RFLP) analysis. Part 2: Bacteria field study
  16. Phylogenetic analysis and discoloration characteristics of major molds inhabiting woods. Part 3. Genus Cladosporium
  17. Identification of biochemical differences between the sapwood and transition zone in Robinia pseudoacacia L. by differential display of proteins
  18. Short Notes
  19. Reduction of formaldehyde emission from light MDF panels by adding chestnut shell flour
  20. On the structure of the active compound in mass deacidification of paper
  21. Meetings
  22. Meetings
  23. Masthead
  24. Masthead
Downloaded on 18.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/hf.2011.176/html
Scroll to top button