The Thermal Behavior of Lyocell Fibers Containing Bis(trimethylsilyl)acetylene

This study focuses on the preparation of carbon fiber precursors from solutions of cellulose in N-methylmorpholine-N-oxide with the addition of bis(trimethylsilyl)acetylene, studying their structural features and evaluating thermal behavior. The introduction of a silicon-containing additive into cellulose leads to an increase in the carbon yield during carbonization of composite precursors. The type of the observed peaks on the differential scanning calorimetry (DSC) curves cardinally changes from endo peaks intrinsic for cellulose fibers to the combination of endo and exo peaks for composite fibers. For the first time, coefficient of thermal expansion (CTE) values were obtained for Lyocell fibers and composite fibers with bis(trimethylsilyl)acetylene (BTMSA). The study of the dependence of linear dimensions of the heat treatment fibers on temperature made it possible to determine the relation between thermal expansion coefficients of carbonized fibers and thermogravimetric curves, as well as to reveal the relationship between fiber shrinkage and BTMSA bis(trimethylsilyl)acetylene content. Carbon fibers from composite precursors are obtained at a processing temperature of 1200 °C. A study of the structure of carbon fibers by X-ray diffraction, Raman spectroscopy, and transmission electron microscopy made it possible to determine the amorphous structure of the fibers obtained.

APPLICATION OF LYOCELL FIBER STRUCTURE FORMATION MECHANISM IN FLAME-RETARDANT MODIFICATION OF LYOCELL FIBER

In order to overcome the disadvantage of Lyocell fiber flammability, two types of flame-retardant finishing liquids, 2-carboxyethyl phenylphosphic acid (CEPPA) and N-hydroxymethyl-3-dimethoxyphosphoacyl propanamide (MDPA), were used in this study to treat Lyocell fiber in two different states: never-dried and dry. The results showed that CEPPA and MDPA can react with the hydroxyl groups of the cellulose and graft onto the Lyocell fiber under appropriate conditions, resulting in increased flame-retardant performance of the fiber, a slight reduction in crystallinity, and a significant decline in mechanical properties. Compared with the dry fiber, the P content and LOI of the fiber obtained by treating the as-spun never-dried Lyocell fiber rose significantly: the P content was higher by 38.9% (for CEPPA) and 20.5% (for MDPA), respectively, while the LOI increased by 6.0% (for CPPA) and 4.0% (for MDPA), respectively, which means that the fiber had better flame-retardant performance. Although the breaking strength of the fiber decreased, it still met the requirements for textiles. In addition, direct flame-retardant treatment of never-dried wet fiber can reduce energy consumption by avoiding repeated drying. Furthermore, the results of this study also have guiding significance for other post-processing procedures for Lyocell fibers, such as dyeing, catalyst infiltration during carbon fiber preparation etc