Abstract

Thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) is grafted from wet bacterial cellulose (WBC) sheets using atom transfer radical polymerization (ATRP). WBC is recognized as a highly swollen biocompatible material with broad application potential. However, native WBC undergoes drying relatively fast and its reswelling ability diminishes after losing a substantial amount of water. In this work PNIPAM is grafted from WBC to slow down its drying, especially at elevated temperatures, which is relevant for biomedical applications. As a primary step, initiator molecules, 2-bromoisobutyryl bromide, are attached to WBC through linkers that are covalently bound to the cellulose hydroxyl groups. Grafting of PNIPAM is then realized via surface-initiated ATRP in a water/methanol mixture leading to WBC-g-PNIPAM. The modification steps are followed via FT-IR, XRD, elemental analysis, and atomic force microscopy. It is concluded that PNIPAM contributes to ca. 22% of the dry mass of WBC-g-PNIPAM. The samples are subjected to repeating swelling and drying steps at 25 °C and drying at 40 °C. The obtained results indicate that grafted PNIPAM significantly reduces drying of the modified WBC and enables better reswelling after treatment at 40 °C with respect to native WBC. The reported synthetic method may also be used for grafting other polymers bringing additional functionalities to WBC.

Highlights

  • Cellulose is the most common, renewable, biodegradable natural polymer resource on earth

  • We present for the first time the surface modification of wet bacterial cellulose (WBC) sheets by a thermosensitive polymer, poly(N-isopropylacrylamide) (PNIPAM), which was grafted to improve the swelling-drying ability of WBC

  • The IR spectrum of WBC contains a broad band in the range of 3400–3300 cm-1 that is attributed to the stretching vibrations of the OH groups of cellulose that are involved in the formation of hydrogen bonds and the band around 2900–2800 cm-1 corresponding to C–H stretching (Ullah et al 2016; Amin et al 2012)

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Summary

Introduction

Cellulose is the most common, renewable, biodegradable natural polymer resource on earth. Novel demanding biomedical applications have brought more attention to this chemically well-recognized material but in a new structural form called nanocellulose. Nanocellulose is the nanostructured product or extract from the native cellulose found in plants, animals, and bacteria. Three main types of nanocellulose have been identified: cellulose nanocrystals (CNCs), nanofibrillated cellulose (NFC) and bacterial cellulose (BC) (Habibi 2014; Dufresne 2012; Klemm et al 2011). BC demonstrates a series of distinguished structural features and properties such as high purity, a high degree of polymerization, high crystallinity, water content up to 99%, and good mechanical stability. These properties have attracted significant interest from both research scientists and industrialists. BC has wide applications in various fields including: medical, food, advanced acoustic diaphragms, etc. (Klemm et al 2011; Czaja et al 2007)

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