Abstract

Temperature profiles through combustion waves in mixtures of ammonium perchlorate (AP) with polymethylmethacrylate (PMM), paraform (PF), and sulphur were obtained by fine W5%Re–W20%Re thermocouples embedded in the strands. The surface temperature, T s , increased with pressure, p (for AP + PF, α = 1 mixture-from 460 °C at p = 0.3 atm to 580 °C at p = 1 atm) and there was a corresponding rise in the burning rate. In contrast, the addition of a catalyst (Cu 2O) had no effect on T s despite a considerable (1.7–1.95 times) increase in the burning rate. The slopes of ln( T − T 0) = f( x) curves reveal a marked increase at T = T ∗ (where T ∗ ranges from 200 °C to 310 °C), probably due to the phase change AP (orthorhombic) → AP (cubic). The departure of T ∗ from the well-known value 240 °C may be ascribed to errors in the thermocouple measurements and to the gasification of PF at T < T ∗ at low pressures. The profiles T( x) and ϕ( x) (where ϕ = dT dx ) were obtained theoretically from a solution of the heat flow equation for a medium with a phase change. An estimate was obtained for the value of ( ϕ 240°+ dT − ϕ 240°− dT ) equal to 1.69 × 10 5 ṁ deg C/cm for the preheat zone in pure AP (where m is mass burning rate). Two maxima of ϕ were observed in the gas phase. The first appears when the thermocouple traverses the NH 3 + HClO 4 flame. The value ( ϕ max) 1 increased with pressure at p ⩽ 1 atm (for AP + PMM, α = 0.75 mixture—from 2.1 × 10 5 deg C/cm at p = 0.34 atm to 4.9 × 10 5 deg C/cm at p = 1 atm). At p = 1 atm ( ϕ max) 1 decreased with increasing p, probably due to thermal inertia of the thermocouple. A simple relationship was obtained for the maximum thermal gradient recorded by a thermocouple. The heat balance at the burning surface is considered. For the mixture under investigation the heat production in the condensed phase at p≤1 atm was insignificant. The addition of Cu 2O increased the thermal gradient in the gas phase near the surface and the burning velocity by about the same extent.

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