TY - JOUR
T1 - Colloidal aspects of Janus-like hairy cellulose nanocrystalloids
AU - Sheikhi, Amir
AU - van de Ven, Theo G.M.
N1 - Funding Information:
Financial support from Natural Sciences and Engineering Research Council (Canada), FPInnovations, Fonds de Recherche du Québec-Nature et technologies (FRQNT, Quebec, Canada), and Centre for Self-Assembled Chemical Structures (CSACS) is gratefully acknowledged. We thank K. Conley for providing peeled CNC suspension images.
Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/5/1
Y1 - 2017/5/1
N2 - For decades, cellulose nanocrystals (CNCs) have been produced by hydrolyzing the disordered cellulose chains of hierarchical fiber structures. These colloidal particles comprise highly ordered arrays of cellulose chains, impeding the physicochemical modifications of inner crystalline layers, which in turn restrict key colloidal properties, such as dispersion stability, functionalizability and charge, response to external fields, and transportation. Controlled oxidation of fibrils permits the partial disintegration of amorphous cellulose chains while maintaining contact with the crystalline body, yielding Janus-like nanoparticles with a needle-shaped crystalline body sandwiched between two disordered cellulose regions (hairs). We refer to these nanoparticles as hairy cellulose nanocrystalloids (HCNC). The protruding soft biopolymer brushes impart significant modifications to the colloidal properties of cellulose nanocrystals, promoting their functionality, charge, stability, and self-assembly. In this article, we embark on detailing how HCNCs behave more like soft nanoparticles as compared to rigid CNCs, explain their fundamental colloidal aspects, and provide a mechanistic overview on how HCNC may expand the horizon of next generation natural soft materials.
AB - For decades, cellulose nanocrystals (CNCs) have been produced by hydrolyzing the disordered cellulose chains of hierarchical fiber structures. These colloidal particles comprise highly ordered arrays of cellulose chains, impeding the physicochemical modifications of inner crystalline layers, which in turn restrict key colloidal properties, such as dispersion stability, functionalizability and charge, response to external fields, and transportation. Controlled oxidation of fibrils permits the partial disintegration of amorphous cellulose chains while maintaining contact with the crystalline body, yielding Janus-like nanoparticles with a needle-shaped crystalline body sandwiched between two disordered cellulose regions (hairs). We refer to these nanoparticles as hairy cellulose nanocrystalloids (HCNC). The protruding soft biopolymer brushes impart significant modifications to the colloidal properties of cellulose nanocrystals, promoting their functionality, charge, stability, and self-assembly. In this article, we embark on detailing how HCNCs behave more like soft nanoparticles as compared to rigid CNCs, explain their fundamental colloidal aspects, and provide a mechanistic overview on how HCNC may expand the horizon of next generation natural soft materials.
UR - http://www.scopus.com/inward/record.url?scp=85013040599&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85013040599&partnerID=8YFLogxK
U2 - 10.1016/j.cocis.2017.02.001
DO - 10.1016/j.cocis.2017.02.001
M3 - Review article
AN - SCOPUS:85013040599
SN - 1359-0294
VL - 29
SP - 21
EP - 31
JO - Current Opinion in Colloid and Interface Science
JF - Current Opinion in Colloid and Interface Science
ER -