TY - JOUR
T1 - Lignin and holocellulose from pecan nutshell as reinforcing fillers in poly (lactic acid) biocomposites
AU - Agustin-Salazar, Sarai
AU - Cerruti, Pierfrancesco
AU - Medina-Juárez, Luis Ángel
AU - Scarinzi, Gennaro
AU - Malinconico, Mario
AU - Soto-Valdez, Herlinda
AU - Gamez-Meza, Nohemi
N1 - Publisher Copyright:
© 2018
PY - 2018/8/1
Y1 - 2018/8/1
N2 - Lignocellulose from agro-food biowaste represents a valuable source of cost-effective structural fillers for wholly renewable polymer composites. In this work, pecan (Carya illinoinensis) nutshell (NS) fiber and its structural components, holocellulose (HC) and acid insoluble lignin (AIL), were isolated, characterized and used as reinforcing fillers to manufacture poly(lactic acid) (PLA) based biocomposites. Thermal, morphological and mechanical properties of the prepared materials were analyzed. NS and HC acted as heterogeneous nucleating agents, potentially able to control PLA physical aging. Moreover, they significantly enhanced the viscoelastic response of PLA, mainly restricting the melt molecular mobility due to hydrodynamic effects and the formation of a three-dimensional particulate network. Flexural tests demonstrated that HC induced a 25% increase in modulus compared to the plain polymer. AIL, conversely, conferred higher ductility to the PLA matrix producing an increase in stress and strain at break of 55% and 65%, respectively. Finally, all the biocomposites showed lower resilience with respect to plain PLA due to the lack of chemical adhesion between filler and matrix. These results emphasize the potential of NS as a source of reinforcing filler in polymer-based biocomposites.
AB - Lignocellulose from agro-food biowaste represents a valuable source of cost-effective structural fillers for wholly renewable polymer composites. In this work, pecan (Carya illinoinensis) nutshell (NS) fiber and its structural components, holocellulose (HC) and acid insoluble lignin (AIL), were isolated, characterized and used as reinforcing fillers to manufacture poly(lactic acid) (PLA) based biocomposites. Thermal, morphological and mechanical properties of the prepared materials were analyzed. NS and HC acted as heterogeneous nucleating agents, potentially able to control PLA physical aging. Moreover, they significantly enhanced the viscoelastic response of PLA, mainly restricting the melt molecular mobility due to hydrodynamic effects and the formation of a three-dimensional particulate network. Flexural tests demonstrated that HC induced a 25% increase in modulus compared to the plain polymer. AIL, conversely, conferred higher ductility to the PLA matrix producing an increase in stress and strain at break of 55% and 65%, respectively. Finally, all the biocomposites showed lower resilience with respect to plain PLA due to the lack of chemical adhesion between filler and matrix. These results emphasize the potential of NS as a source of reinforcing filler in polymer-based biocomposites.
KW - Biocomposites
KW - Holocellulose
KW - Lignin
KW - Pecan nutshell
KW - Poly (lactic acid)
UR - http://www.scopus.com/inward/record.url?scp=85046129320&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2018.04.120
DO - 10.1016/j.ijbiomac.2018.04.120
M3 - Artículo
C2 - 29702173
AN - SCOPUS:85046129320
SN - 0141-8130
VL - 115
SP - 727
EP - 736
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
ER -