Abstract
Using isocyanate-functionalized Kraft lignin as a reactive macromonomer for the preparation of polyurethane foams by a prepolymer technique is a well-known strategy to incorporate the biomacromolecule into a higher value polymer material. However, as of today the mechanical properties of the resulting materials are still insufficient for a number of possible applications. One reason for this limitation is that the reaction pathway and the morphological arrangement of such foams is of uttermost complexity and depends on a large number of influencing material-intrinsic factors. One important parameter is the reactivity of the functionalized lignin, which has a great impact on the interphase reaction kinetics and thus, on the geometry and mechanical properties of the resulting polyurethane foams. The reactivity is implied, amongst others, by the electron affinity of the isocyanate moiety. Herein, we investigate the reactivity of Kraft lignin modified with different commercially used isocyanates in the reaction with conventional polyols. Therefore, differently reactive prepolymers were synthesized, characterized and polyurethane foams were prepared thereof by using these compounds and the foam formation kinetics, morphological as well as mechanical properties were investigated. Finally, the results were supported by quantum mechanical calculations of the electron affinities of representative model compounds for the lignin-based prepolymers. This work gives rise to a better understanding of the effect of the reactivity and isocyanate structure linked to Kraft lignin on the polyurethane formation and enables rational choice of the isocyanate for pre-functionalization of lignin to prepare materials with better mechanical performance.
Highlights
Polyurethanes (PUs) are a class of highly interesting materials due to their versatility that makes them valuable for various fields of day-to-day applications, such as coatings, flame retardants, insulations, adhesives, paints and foams (Chattopadhyay and Raju, 2007)
When lignin was functionalized with toluene diisocyanate (TDI) a lower NCO content of 1.14 mmol/g is obtained and in KL-hexamethylene diisocyanate (HDI) 0.97 mmol/g isocyanate moieties were linked to the lignin
When this amount has been abreacted, two factors are the cause that significantly more unreactive OH groups can be functionalized by using methylene diisocyanate (MDI) than by using TDI, which both are caused by the low reactivity of the NCO group in position 2 of the TDI (Bailey et al, 1956): First, the concentration of isocyanates in solution is decreased during the reaction of the TDI, second, the reactivity of the second NCO may not be high enough to further react intramolecularly with the lignin
Summary
Polyurethanes (PUs) are a class of highly interesting materials due to their versatility that makes them valuable for various fields of day-to-day applications, such as coatings, flame retardants, insulations, adhesives, paints and foams (Chattopadhyay and Raju, 2007). PU foams show unique material characteristics, such as thermal insulating, low volumetric weight and Reactivity of Isocyanate-Functionalized Lignins versatile mechanical properties (Singh and Jain, 2008; Yang et al, 2015; Liu et al, 2017). Polyurethanes are products of an addition reaction of a polyol and a (poly)isocyanate, respectively, and it can be considered as phase separated polymer blends which consist of alternating hard and soft segments linked to each other by different chemical as well as physical interaction means (Petrovic and Ferguson, 1991). To obtain the desired foam structure providing good material properties, urethane formation (crosslinking) of the polymer and vitrification occurs in situ during the blowing reaction, with an immobilized blow structure in the end. Perfectly harmonizing diffusion, reaction kinetics of the single processes (blow reaction vs. crosslinking reactions) and thermodynamic properties (e.g., glass transition/vitrification) are a crucial requirement (Delebecq et al, 2013)
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