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Preparation of oxidized nanocellulose by using potassium dichromate
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Abstract
Nanocellulose (NC) derivatives are being used in a wide variety of high-quality functional applications. One of them is oxidized nanocellulose (ONC), which has been used in biomedical and pharmaceutical applications due to its biodegradable, biocompatible, hemostatic, and antibacterial properties. In this work, ONC was synthesized using potassium dichromate as an oxidizing agent. The structure of ONC was investigated by means of ultraviolet spectrophotometry (UV), fourier transforms infrared spectroscopy (FTIR), X-ray diffraction (XRD), atomic force microscopy (AFM), and thermogravimetric analysis (TGA). The results showed that the primary hydroxyl groups of NC were selectively oxidized to carboxyl groups and their content of 1.36 mmol/g was achieved. The appearance of a new peak (1721 cm− 1) in the FTIR- spectra related to the C = O group was observed. The change of ONC degree of crystallinity (DC) from 88.0–82.5% was revealed and the sizes of the unit cells of both NC and ONC were calculated. The thermal stability of ONC decreased compared to NC. The oxidation process of NC leads to a change in the shape and size of particles from acicular to spherical with a narrow particle size distribution. It was shown that ONC has the ability to accumulate charge on its surface.
Springer Science and Business Media LLC
Title: Preparation of oxidized nanocellulose by using potassium dichromate
Description:
Abstract
Nanocellulose (NC) derivatives are being used in a wide variety of high-quality functional applications.
One of them is oxidized nanocellulose (ONC), which has been used in biomedical and pharmaceutical applications due to its biodegradable, biocompatible, hemostatic, and antibacterial properties.
In this work, ONC was synthesized using potassium dichromate as an oxidizing agent.
The structure of ONC was investigated by means of ultraviolet spectrophotometry (UV), fourier transforms infrared spectroscopy (FTIR), X-ray diffraction (XRD), atomic force microscopy (AFM), and thermogravimetric analysis (TGA).
The results showed that the primary hydroxyl groups of NC were selectively oxidized to carboxyl groups and their content of 1.
36 mmol/g was achieved.
The appearance of a new peak (1721 cm− 1) in the FTIR- spectra related to the C = O group was observed.
The change of ONC degree of crystallinity (DC) from 88.
0–82.
5% was revealed and the sizes of the unit cells of both NC and ONC were calculated.
The thermal stability of ONC decreased compared to NC.
The oxidation process of NC leads to a change in the shape and size of particles from acicular to spherical with a narrow particle size distribution.
It was shown that ONC has the ability to accumulate charge on its surface.
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