Abstract

Dicarboxylate nanocrystalline cellulose (DCNC) polyelectrolytes were prepared from nanocrystalline cellulose (NCC) by introducing carboxylate units at the C-2 and C-3 positions of a glucose moiety through a two-step selective oxidation process. The polyelectrolyte nature of the DCNC was investigated by measuring the water uptake capacity with a customized ion exchange system. The equilibrium water uptake capacity of DCNC was almost ten times greater than that of conventional C-6 functionalized monocarboxylated NCC. The conversion of NCC to DCNC ensured the presence of a large number of dissociable electrolytic ions and high degrees of conformational freedom in the material to generate high osmotic pressure. Conductivity and dynamic light-scattering measurements were performed to relate the water uptake capacity with the chemical and structural changes of the polyelectrolytes. Furthermore, it was observed that the ionic strength of the solution played a critical role in controlling the water uptake capacity of the material. Polyelectrolytes (PEs) with high water uptake prepared from cellulose-type polysaccharides are promising because of their excellent biodegradability. In this work, utilizing a two-step selective oxidation process a new type dicarboxylate nanocrystalline cellulose (DCNC) PE was prepared. Carboxylate units were introduced at the C-2 and C-3 positions of a glucose moiety to ensure the presence of a large number of dissociable electrolytic ions. It was observed that the equilibrium water uptake capacity of the prepared DCNC was almost ten times greater than that of conventional C-6 functionalized monocarboxylated nanocrystalline cellulose.

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