Hygroscopicity of nitrocellulose with different nitrogen content

Abstract

Research on the hygroscopic behavior of NC is essential because it affects the mechanical properties, combustion properties, and safe storage of NC‐based products. In this study, Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), and scanning electron microscopy (SEM) are used to characterize the chemical structure, crystal structure, and microscopic morphology of NC, respectively. The moisture adsorption isotherms of NC fibers with different nitrogen content are determined by dynamic vapor sorption (DVS) and fitted with Hailwood‐Horrobin (H−H) and Guggenheim‐Anderson‐de Boer (GAB) models. The specific surface area and surface energy of NC are also measured by inverse gas chromatography (IGC). The results show that as the nitrogen content of NC increases, the intensity of the −OH characteristic absorption peak is weakened, the crystallinity does not change much, the number of cracks and pores on the NC fiber surface increases, and the equilibrium moisture content (EMC) of the NC decreases in general. In addition, the fitting results based on the H−H and GAB models show that, under low humidity conditions, the EMC value of NC is determined by the adsorbed water content of the monolayer, which is mainly related to the −OH content in NC. However, with the increase of humidity, the EMC value of NC is gradually determined by the multilayer adsorbed water content, which is influenced by both the nitrogen content and the fiber cleavage structure. Meanwhile, the IGC results show that the surface energy of the NC consists mainly of the dispersive surface energy (values >46 mJ m−2), with the specific surface energy contributing approximately 25 mJ m−2. The total surface energy of NC and the bonding strength between NC molecules and water molecules decrease with increasing nitrogen content.

Cellulose Nitrates-Blended Composites from Bacterial and Plant-Based Celluloses

“…As the degree of substitution increased, the nitrogen content of the CN samples (Table 2) also increased, while the intensity of hydroxyl peaks became less pronounced. This observation aligns with previous studies reported in [8,11,37,57,58]. Specifically, the CN NA + MC samples exhibited a lower hydroxyl intensity compared to the CN MA samples, consistent with their higher nitrogen content.…”