US EPA

736046 

Journal Article 

Thermal stability and flame retardancy of polyurethanes 

Chattopadhyay, DK; Webster, DC 

2009 

1 

Progress in Polymer Science
ISSN: 0079-6700 

34 

10 

1068-1133 

10.1016/j.progpolymsci.2009.06.002 

WOS:000270617800002 

The thermal stability and flame retardancy of polyurethanes is reviewed. Polyurethanes (PUs) are an important class of polymers that have wide application in a number of different industrial sectors. More than 70% of the literature that deals with PUs evaluates their thermal stability or flame retardancy and attempts to provide a structure–property correlation. The importance of studying thermal degradation, understanding the processes occurring during thermal stress as well as the parameters affecting the thermal stability of PUs are essential in order to effectively design polyurethanes having tailor-made properties suitable for the particular environment where they are to be used. A detailed description of TGA, TGA-MS and TGA-FTIR methods for studying the decomposition mechanism and kinetics is also a part of this review. In general, thermal decomposition of PUs begins with the hard segment (HS) and a number of parameters govern a polyurethane's thermal stability. Detailed description of the parameters such as HS, soft segment (SS) and chain extender (CE) structure and molecular weight, NCO:OH ratio, catalyst nature and crosslink density that affect the nature of PU degradation is given. Descriptions of approaches to improve the thermal stability in PUs such as formation of poly(urethane-isocyanurate), poly(urethane-oxazolidone) and poly(urethane-imide) in addition to other methods such as PUs with an s-triazine ring or increased aromatic ring concentration, azomethane linkages as well as use of hyperbranched polyols as crosslinking agents is given. A part of the review is also concentrated on the improvement of thermal stability via hybrid formation such as the incorporation of appropriate amounts of fillers, e.g., nano-silica; Fe2O3; TiO2; silica grafting; nanocomposite formation using organically modified layered silicates; incorporation of Si–O–Si crosslinked structures via sol–gel processes; and the incorporation of polyhedral oligomeric silsesquioxane (POSS) structures into the PU backbone or side chain. Incorporation of carbon nanotubes (CNT) into PUs and the use of functionalized fullerenes in PUs are also described as these are the newest tools to obtain good thermal stability and flame retardancy. Part of the review also concentrates on the process that occurs during burning of PUs, flame retardant mechanisms and different additives or reactive type flame retardants used in the PU industry. The use and working function of expandable graphite and melamine as additive type flame retardants are shown. Description of the use of different reactive type organophosphorus compounds, cyclotriphosphazenes, aziridinyl curing agents in aqueous polyurethane dispersions (PUDs), organoboron compounds and organosilicon compounds for improving flame retardancy is also given. 

Polyurethane; Thermal stability; Polyurethane-isocyanurate; Polyurethane-oxazolidone; Polyurethane-imide; Nanocomposite; POSS; Carbon nanotube; Fullerenes; Flame retardancy; Functionalization