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Publication Date:
December 2007
ISSN:
1437-434X
DOI:
10.1515/HF.2008.004

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Holzforschung

International Journal of the Biology, Chemistry, Physics, and Technology of Wood

Editor-in-Chief: Faix, Oskar

Editorial Board Member: Daniel, Geoffrey / Militz, Holger / Rosenau, Thomas / Salmen, Lennart / Sixta, Herbert / Vuorinen, Tapani / Argyropoulos, Dimitris S. / Balakshin, Yu / Barnett, J. R. / Berry, Richard / Burgert, Ingo / Evans, Robert / Evtuguin, Dmitry V. / Frazier, Charles E. / Fukushima, Kazuhiko / Gellerstedt, Göran / Gindl-Altmutter, Wolfgang / Glasser, W. G. / Heitner, Cyril / Holmbom, Bjarne / Isogai, Akira / Kadla, John F. / Kleen, Marjatta / Koch, Gerald / Lachenal, Dominique / Mansfield, Shawn D. / Morrell, J.J. / Niemz, Peter / Pizzi, Antonio / Ragauskas, Arthur J. / Ralph, John / Rice, Robert W. / Salin, Jarl-Gunnar / Schmitt, Uwe / Schultz, Tor P. / Schwanninger, Manfred / Sipilä, Jussi / Tamminen, Tarja / Viikari, Liisa / Welling, Johannes / Willför, Stefan / Yoshihara, Hiroshi

8 Issues per year

Increased IMPACT FACTOR 2011: 1.748
5-year IMPACT FACTOR: 1.838
Rank 2 out of 21 in category Materials Science, Paper & Wood and 10 out of 59 in category Forestry in the 2011 Thomson Reuters Journal Citation Report/Science Edition.

VolumeIssuePage

Issues

Isolation and characterization of lignins from Eucalyptus grandis Hill ex Maiden and Eucalyptus globulus Labill. by enzymatic mild acidolysis (EMAL)

Anderson Guerra1 / Lucian A. Lucia2 / Dimitris S. Argyropoulos3

1Organic Chemistry of Wood Components Laboratory, Department of Forest Biomaterials Science and Engineering, North Carolina State University, Raleigh, NC, USA and Centro de Biotecnología, Universidad de Concepción, Concepción, Chile

2Organic Chemistry of Wood Components Laboratory, Department of Forest Biomaterials Science and Engineering, North Carolina State University, Raleigh, NC, USA

3Organic Chemistry of Wood Components Laboratory, Department of Forest Biomaterials Science and Engineering, North Carolina State University, Raleigh, NC, USA

Corresponding author. Organic Chemistry of Wood Components Laboratory, Department of Forest Biomaterials Science and Engineering, North Carolina State University, Raleigh, NC 27695-8005, USA

Citation Information: Holzforschung. Volume 62, Issue 1, Pages 24–30, ISSN (Online) 1437434X, ISSN (Print) 00183830, DOI: 10.1515/HF.2008.004, December 2007

Publication History:
Received:
2007-04-13
Accepted:
2007-07-23
Published Online:
2007-12-05

Abstract

Despite the growing importance of Eucalyptus wood as raw material for pulp and paper, there is a lack of knowledge on the chemistry of their macromolecular components. The present paper addresses this issue by applying the recently developed protocol for isolating enzymatic mild acidolysis lignins (EMAL) from Eucalyptus grandis, Eucalyptus globulus and the softwood species Douglas fir and white fir, which were used for comparative purposes. The structures of EMALs were investigated by quantitative 31P NMR, DFRC/31P NMR (derivatization followed by reductive cleavage followed by quantitative 31P NMR) and size exclusion chromatography (SEC). Overall, the yields of EMALs isolated from Eucalyptus were higher than those from the softwoods examined. Lignin from E. globulus was found to contain higher contents of arylglycerol-β-aryl ether structures, free phenolic hydroxyl groups and syringyl-type units than lignin from E. grandis. New insights provided by the DFRC/31P NMR revealed that up to 62.2% of arylglycerol-β-aryl ether structures in E. globulus are uncondensed, while in E. grandis the amount of such uncondensed structures was found to be lower than 48%. SEC analyses showed that lignins from E. grandis and softwoods associate in greater extension than lignin from E. globulus.

Keywords: derivatization followed by reductive cleavage (DFRC); enzymatic mild acidolysis lignin (EMAL); Eucalyptus; lignin; milled wood lignin (MWL); 31P nuclear magnetic resonance spectroscopy

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