New In-Flame Flammability Testing Method Applied to Monitor Seasonal Changes in Live Fuel

Improving the accuracy of fire behavior prediction requires better understanding of live fuel, the dominant component of tree crowns, which dictates the consumption and energy release of the crown fire flame-front. Live fuel flammability is not well represented by existing evaluation methods. High-flammability live fuel, e.g., in conifers, may maintain or increase the energy release of the advancing crown fire flame-front, while low-flammability live fuel, e.g., in boreal deciduous stands, may reduce or eventually suppress flame-front energy release. To better characterize these fuel–flame-front interactions, we propose a method for quantifying flammability as the fuel’s net effect on (contribution to) the frontal flame energy release, in which the frontal flame is simulated using a methane diffusion flame. The fuel’s energy release contribution to the methane flame was measured using oxygen consumption calorimetry as the difference in energy release between the methane flame interacting with live fuel and the methane flame alone. In-flame testing resulted in fuel ignition and consumption comparable to those in wildfires. The energy release contribution of live fuel was significantly lower than its energy content measured using standard methods, suggesting better sensitivity of the proposed metric to water content- and oxygen deficiency-associated energy release reductions within the combustion zone.

Semi-Crystalline Hydrophobic Polyamidoamines: A New Family of Technological Materials?

The hitherto known polyamidoamines (PAAs) are not suitable as structural materials because they are usually water-soluble or swellable in water. This paper deals with the synthesis and characterization of semi-crystalline hydrophobic PAAs (H-PAAs) by combining different bis-sec-amines with bis-acrylamides obtained from C6–C12 bis-prim-amines. H-PAAs were initially obtained in a solution of benzyl alcohol, a solvent suitable for both monomers and polymers. Their number average molecular weights, M¯n, which were determined with 1H-NMR by evaluating the percentage of their terminal units, varied from 6000 to >10,000. The solubility, thermal properties, ignitability and water resistance of H-PAAs were determined. They were soluble in organic solvents, semi-crystalline and thermally stable. The most promising ones were also prepared using a bulk process, which has never been previously reported for PAA synthesis. In the form of films, these H-PAAs were apparently unaffected by water. The films underwent tensile and wettability tests. They showed similar Young moduli (260–263 MPa), whereas the maximum stress and the stress at break depended on the number of methylene groups of the starting bis-acrylamides. Their wettability was somewhat higher than that of common Nylons. Interestingly, none of the H-PAAs considered, either as films or powders, ignited after prolonged exposure to a methane flame.