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Experimental investigation of ablation and pyrolysis processes of carbon-phenolic ablators in atmospheric entry plasmas

机译:大气进入等离子体中碳酚烧蚀器的烧蚀和热解过程的实验研究

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We study the ablation and transient pyrolysis outgassing of the carbon-phenolic ablators AQ61 and Asterm in air and nitrogen plasmas. We investigate their resistance to high heating conditions, and characterize gas-surface interaction phenomena, including the interaction of the pyrolysis gases with the hot plasma flow. The experiments were carried out in the Plasmatron facility of the von Karman Institute for Fluid Dynamics. The aero-thermodynamic environment of atmospheric entry in the boundary layer of a test object was selected with surface temperatures between 1900 K and 2800 K, and test chamber pressures of 15 hPa, 100 hPa, and 200 hPa. Those conditions led to recession rates between 39 μm/s and 83 μm/s in air plasmas. Micrographs revealed oxidation of the char layer and carbon fibers. Carbon deposition in the form of soot was observed on samples tested in nitrogen, contrary to air ablation where charred resin was not found at the surface. We propose an approach to estimate the temporally resolved pyrolysis outgassing rate, based on the emission signature of pyrolysis products and the volume change of the sample. The temporal recession rate was obtained from high-speed camera imaging. This enabled evaluation of the surface recession as a function of the pyrolysis outgassing rate, which was then compared to numerical estimates predicted by thermochemical equilibrium tables. The thermochemical equilibrium model generally underpredicted experimental recession rates, particularly at low pressure (15 hPa). Stronger mechanical failure of the material was ruled out as experiments at the same test conditions in nitrogen plasmas did not show any significant recession. Micrographs did not indicate internal oxidation of the material, neither was spallation observed during the low pressure experiments.
机译:我们研究了在空气和氮气等离子体中碳-酚类烧蚀器AQ61和Asterm的烧蚀和瞬时热解出气。我们研究了它们对高温条件的抵抗力,并表征了气体表面相互作用现象,包括热解气体与热等离子体流之间的相互作用。实验是在冯·卡曼流体动力学研究所的Plasmatron设备中进行的。选择表面温度介于1900 K和2800 K之间,测试室压力为15 hPa,100 hPa和200 hPa的空气进入测试对象边界层的空气热力学环境。这些条件导致空气等离子体的衰退率在39μm/ s和83μm/ s之间。显微照片显示炭层和碳纤维的氧化。在氮气中测试的样品上观察到以烟灰形式的碳沉积,这与空气消融相反,后者在表面未发现烧焦的树脂。我们提出了一种方法,根据热解产物的排放特征和样品的体积变化,估算时间分辨的热解脱气率。时间衰退率是从高速相机成像获得的。这样就可以根据热解出气率对表面退缩进行评估,然后将其与热化学平衡表预测的数值估算值进行比较。热化学平衡模型通常会低估实验衰退率,尤其是在低压(15 hPa)下。由于在相同的测试条件下在氮气等离子体中进行的实验未显示出任何明显的衰退,因此排除了材料更强的机械故障。显微照片没有表明材料的内部氧化,在低压实验中也没有观察到散裂。

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