Flexible Polyurethane Foam: A Literature Review of Thermal Decomposition Products and Toxicity

1989 ◽  
Vol 8 (6) ◽  
pp. 1139-1175 ◽  
Author(s):  
R. A. Orzel ◽  
S. E. Womble ◽  
F. Ahmed ◽  
H. S. Brasted

This report presents a comprehensive literature review of the toxicity of the combustion products of flexible polyurethane foam and the thermal decomposition products of this polymer. Combustion toxicity results obtained using different test methods but measuring the same toxicologic endpoints were compared. That is, time to incapacitation and time to death using the USF and FAA test methods were compared. Also, LC50 values using the DIN, NBS, and University of Pittsburgh tests were compared. The results indicate that despite the use of different test methods, foam densities, formulations, fire retardants, and other additives, combustion toxicity data were generally considered comparable when similar endpoints were compared. Neither CO nor HCN appeared to be the primary cause of death due to the combustion products of flexible polyurethane foam, although they were probably contributory factors. Under conditions of oxidation and pyrolysis, polyurethane foams decomposed into a liquid polyol component and a “yellow smoke.” The polyol decomposed into CO, CO2, and low-molecular-weight hydrocarbons including ketones, ethers, and/or esters. At high temperatures (greater than 800°C), the “yellow smoke” decomposed into HCN and other nitrogen-containing compounds such as acetonitrile, acrylonitrile, and benzonitrile. Twice as much HCN was produced under pyrolytic conditions as in oxygen-rich atmospheres. Various amounts and types of other combustion compounds were produced, depending on the temperature and oxygen availability.

1988 ◽  
Vol 7 (2) ◽  
pp. 201-220 ◽  
Author(s):  
P.K. Johnston ◽  
E. Doyle ◽  
R.A. Orzel

A comprehensive literature review on the thermal decomposition products and combustion toxicity of phenolics is presented. The major decomposition products of phenolics appear to be CO, CO2, H2O, and methane. Smaller quantities of H2, formaldehyde, and other volatile organics, including phenol, methylphenols, and dimethylphenols, also appear to be produced. The types and quantities of thermal decomposition products and the temperatures at which they are produced depend on numerous factors, including the resin structure and formulation and the conditions of degradation. Phenolics produced products that were indicated to be more acutely toxic than other cellular plastics tested by one researcher and were described as “more toxic than wood” by another researcher. Carbon monoxide appears to be the major toxicant produced by the combustion of phenolics. Sensory irritation as indicated by reduced respiratory rate may be due to formaldehyde production; however, sensory irritation is lower than that produced by wood.


1988 ◽  
Vol 7 (2) ◽  
pp. 139-200 ◽  
Author(s):  
P.K. Johnston ◽  
E. Doyle ◽  
R.A. Orzel

A comprehensive literature review on the thermal decomposition products and combustion toxicity of acrylics is presented. The types of products produced by the thermal decomposition of acrylic polymers vary widely. At lower temperatures, simple methacrylate polymers are degraded almost entirely to monomer, whereas simple acrylate polymers are degraded primarily to chain fragments and the alcohols corresponding to the ester groups. More complex methacrylate and acrylate polymers appear to be degraded primarily to the olefins corresponding to the ester groups. The major products formed through the thermal decomposition of polyacrylonitrile include HCN, NH3, CO, CO2, and various nitrile compounds. The decomposition of acrylonitrile copolymers (e.g., acrylic and modacrylic fibers) can result in the release of additional compounds. In general, modacrylic combustion products appear to be more acutely toxic than those of other acrylic materials tested or wood. Modacrylic produced a shorter time to incapacitation and time to death than poly(methyl methacrylate) in the FAA test, and, in the NBS test, the LC50 was more than fivefold lower than that for polyacrylonitrile. In addition, the LC50 of modacrylic in the University of Pittsburgh test was an order of magnitude lower than that for the standard test material, Douglas fir.


1983 ◽  
Vol 23 (2) ◽  
pp. 142-150 ◽  
Author(s):  
D. A. Purser ◽  
P. Buckley

A study has been made of the mechanisms of incapacitation resulting from exposure to atmospheres of thermal decomposition products from polymeric materials. Individual cynomolgus monkeys were exposed to atmospheres increasing in separate experiments from very low concentrations until early physiological signs of incapacitation were detected. Atmospheres studied included thermal decomposition products of polyacrylonitrile, polyurethane foam, wood, polypropylene, polystyrene and nylon produced under pyrolytic or oxidative conditions at a range of temperatures. For some atmospheres the toxicity was dominated by signs of upper and lower respiratory tract irritance, which consisted of dyspnoea and hyperventilation during exposure. The condition of the animals appeared normal within 1–2 hours after exposure, but following exposures to atmospheres from 2 materials, flexible polyurethane foam and polypropylene, signs of late lung inflammatory responses similar to those occurring in some human fire survivors were observed 15–48 hours after exposure.


1988 ◽  
Vol 7 (2) ◽  
pp. 221-242 ◽  
Author(s):  
V. Purohit ◽  
R.A. Orzel

This report presents a comprehensive literature review of the thermal decomposition products of polypropylene evolved under pyrolytic and oxidative conditions and the acute toxicity of combustion products of this polymer. Generally, the pyrolysis products of polypropylene (300–700°C) were aliphatic saturated and unsaturated hydrocarbons. The combustion of polypropylene in air (200–600°C) produced oxygenated hydrocarbons, aromatic hydrocarbons, aliphatic hydrocarbons, CO, CO2, and H2O. In general, as combustion temperature and time increased, the proportions of oxygenated and aliphatic hydrocarbons decreased, whereas the proportion of aromatic hydrocarbons increased. Using the University of San Francisco/National Aeronautical and Space Administration (USF/NASA) method under the fixed temperature program, time to death in mice caused by the combustion products of polypropylene decreased as the temperature was increased. Under the rising temperature mode, time to death decreased when polypropylene was combusted under airflow as compared to no airflow conditions. CO levels generated by the combustion of polypropylene were sufficient to produce the lethal effects observed. Using a test method developed at the University of Michigan, the combustion products of polypropylene were found to be 26 times more toxic under dynamic conditions (rising temperature) than under static conditions (fixed temperature).


2021 ◽  
Vol 46 ◽  
pp. 146867832098218
Author(s):  
Yangui Chen ◽  
Hongzhou He ◽  
Zhongqing Liu

Accurate thermal decomposition mechanism and kinetic parameters are helpful to analyze the combustion process of flexible polyurethane foam. The thermal decomposition process of flexible polyurethane foam products (amine derivatives) was ignored in the past. Three thermal decomposition mechanisms of flexible polyurethane foam were proposed according to the thermogravimetry experiment of flexible polyurethane foam in the nitrogen atmosphere, two of which included the thermal decomposition of amine derivatives. The global search algorithm was proposed to estimate the kinetic parameters of the thermal decomposition of solid material. The results show that the global search algorithm is efficient and accurate in estimating kinetic parameters. The results also show the thermal decomposition mechanism including the carbodiimide and polycarbondiimide can well describe the thermal decomposition process of flexible polyurethane foam and amine derivatives. The activation energy, pre-exponential factor, and reaction order of flexible polyurethane foam are 187.3 kJ mol−1, 1015.6 s−1, and 1.22, respectively.


Sign in / Sign up

Export Citation Format

Share Document