Abstract
Crab chitin was sulfated under heterogeneous conditions using sulfamic acid in N'N-dimethylformamide to selectively sulfate the microfibril surface. The degree of sulfation followed a first order kinetics assuming a limited available reaction sites on the surface leveling off at bulk degree-of-substitution of 0.4. The reaction rate was proportional to the square of sulfamic acid concentration, suggesting involvement of two sulfamic acid molecules in a reaction. When washed with water after sulfation, the crab shell chitin fragments were anisotropically swollen in the helicoidal direction, revealing regular alternating birefringence under optical microscope. Further mechanical treatment with high-pressure homogenizer lead to slender nanofibrils, whose dimaters were of the order of 6 nm according to turbidimetric analysis, in agreement with the Scherrer size estimated from X-ray diffraction line broadening. Both AFM and TEM measurement showed presence further smaller fragments with diameter of 3-4 nm and length of ~300 nm. The current approach presents a rapid and efficient modification to chitin, and a strategy for the preparation of stable nanochitins suspension.
Supplementary materials
Title
Supporting Information: Surface sulfation of crab chitin for anisotropic swelling and nanodispersion
Description
Scheme of heterogeneous sulfation of chitin, Calculation of fibril cross-section from the turbidimetric data, Polarized optical micrographs, Atomic force micrographs,X-ray diffraction of chitin, sulfated chitin and nanochitin and corresponding Scherrer size, Elemental analysis data used in the study
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