Abstract

Bleached and unbleached pulp fibers were treated with 2,2,6,6-tetramethylpyperidine-1-oxyl (TEMPO) mediated oxidation to obtain cellulose nanofibrils (CNFs). The resulting bleached and unbleached CNFs were mixed with salicylic acid (0, 5, 10, 20 wt%) before casting and freeze-drying or 3D-printing. A series of methods were tested and implemented to characterize the CNF materials and the porous structures loaded with salicylic acid. The CNFs were characterized with atomic force microscopy and laser profilometry, and release of salicylic acid was quantified with UV-visible absorbance spectroscopy, conductivity measurements, and inductive coupled plasma mass spectrometry (ICP-MS). Fourier-transform infrared spectroscopy (FTIR) complemented the analyses. Herein, we show that aerogels of bleached CNFs yield a greater release of salicylic acid, compared to CNF obtained from unbleached pulp. The results suggest that biodegradable constructs of CNFs can be loaded with a plant hormone that is released slowly over time, which may find uses in small scale agricultural applications and for the private home market.

Highlights

  • Defending crops against airborne pathogens and insects is a multimillion dollar industry that has severe impacts on the environment and human health [1]

  • The results suggest that biodegradable constructs of cellulose nanofibrils (CNFs) can be loaded with a plant hormone that is released slowly over time, which may find uses in small scale agricultural applications and for the private home market

  • After TEMPO-mediated oxidation the cellulose nanofibrils will have a higher carboxyl group content, compared to nanofibrils that have been produced without chemical pretreatment [27]

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Summary

Introduction

Defending crops against airborne pathogens and insects is a multimillion dollar industry that has severe impacts on the environment and human health [1]. Salicylic acid plays a critical role in a parallel resistance pathway called systemic acquired resistance (SAR). This pathway is non-specific and long-lasting, and protects the plant against a broad range of microorganisms [5]. This means that when a plant is infected by a pathogen, the SAR response ensures that non-infected and distal plant tissue is warned about the incoming threat and causes upregulation of a large number of pathogenesis-related genes [6]

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