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Properties versus application requirements of solubilized lignins from an elm clone during different pre-treatments.
Eugenio, María E; Martín-Sampedro, Raquel; Santos, José I; Wicklein, Bernd; Martín, Juan A; Ibarra, David.
Afiliação
  • Eugenio ME; Forestry Products Department, Forest Research Center, INIA, Ctra de la Coruña Km 7.5, Madrid 28040, Spain.
  • Martín-Sampedro R; Forestry Products Department, Forest Research Center, INIA, Ctra de la Coruña Km 7.5, Madrid 28040, Spain; Instituto de Ciencia de Materiales de Madrid (ICMM), Consejo Superior de Investigaciones Científicas (CSIC), Sor Juana Inés de la Cruz 3, Cantoblanco, Madrid 28049, Spain.
  • Santos JI; General Services of Research SGIKER, University of the Basque Country (UPV/EHU), Edificio Joxe Mari Korta Avda. Tolosa 72, Donostia-San Sebastian 20018, Spain.
  • Wicklein B; Instituto de Ciencia de Materiales de Madrid (ICMM), Consejo Superior de Investigaciones Científicas (CSIC), Sor Juana Inés de la Cruz 3, Cantoblanco, Madrid 28049, Spain.
  • Martín JA; Departamento de Sistemas y Recursos Naturales, ETSI Montes, Forestal y del Medio Natural, Universidad Politécnica de Madrid, c. José Antonio Novais 10, Madrid 28040, Spain.
  • Ibarra D; Forestry Products Department, Forest Research Center, INIA, Ctra de la Coruña Km 7.5, Madrid 28040, Spain. Electronic address: ibarra.david@inia.es.
Int J Biol Macromol ; 181: 99-111, 2021 Jun 30.
Article em En | MEDLINE | ID: mdl-33757853
ABSTRACT
Kraft pulping, organosolv process and acid hydrolysis were applied on an elm clone. The solubilized lignins were recovered and analyzed. Kraft pulping and acid hydrolysis led to lignins with higher phenolic OH content as result of extensive cleavage of ß-O-4' linkages, as revealed by 13C solid state and 13C-1H heteronuclear single quantum coherence nuclear magnetic resonance. This depolymerization also yielded lower molecular weight lignins inferred by size exclusion chromatography. Contrarily, organosolv process gave rise to a lignin with a more preserved structure, maintaining a large number of ß-O-4' linkages. Consequently, organosolv lignin presented lower phenolic OH content and higher molecular weight. Moreover, the high content of the labile native ß-O-4' linkages in organosolv lignin resulted in a lower thermostability as compared to the kraft and acid lignins. On the other hand, the solubilized lignins from kraft and acid processes displayed an enrichment of S-units, whereas lignin from organosolv process was slightly enriched in G-units, containing all of them different native as well as pre-treatment derived units. These results could help to increase the inventory of lignin sources available for future lignin-based products, for which knowledge of the lignin properties versus application requirements is crucial.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ulmus / Lignina Idioma: En Revista: Int J Biol Macromol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ulmus / Lignina Idioma: En Revista: Int J Biol Macromol Ano de publicação: 2021 Tipo de documento: Article