Bullock M A, Stoker C R, McKay C P, Zent A P
Laboratory for Atmospheric and Space Physics, University of Colorado, Boulder 80309-0392, USA. ZODIAC::BULLOCK
Icarus. 1994 Jan;107(1):142-54. doi: 10.1006/icar.1994.1012.
The Viking Gas Chromatograph Mass Spectrometer failed to detect organic compounds on Mars, and both the Viking Labeled Release and the Viking Gas Exchange experiments indicated a reactive soil surface. These results have led to the widespread belief that there are oxidants in the martian soil. Since H2O2 is produced by photochemical processes in the atmosphere of Mars, and has been shown in the laboratory to reproduce closely the Viking LR results, it is a likely candidate for a martian soil oxidant. Here, we report on the results of a coupled soil/atmosphere transport model for H2O2 on Mars. Upon diffusing into the soil, its concentration is determined by the extent to which it is adsorbed and by the rate at which it is catalytically destroyed. An analytical model for calculating the distribution of H2O2 in the martian atmosphere and soil is developed. The concentration of H2O2 in the soil is shown to go to zero at a finite depth, a consequence of the nonlinear soil diffusion equation. The model is parameterized in terms of an unknown quantity, the lifetime of H2O2 against heterogeneous catalytic destruction in the soil. Calculated concentrations are compared with a H2O2 concentration of 30 nmoles/cm3, inferred from the Viking Labeled Release experiment. A significant result of this model is that for a wide range of H2O2 lifetimes (up to 10(5) years), the extinction depth was found to be less than 3 m. The maximum possible concentration in the top 4 cm is calculated to be approximately 240 nmoles/cm3, achieved with lifetimes of greater than 1000 years. Concentrations higher than 30 nmoles/cm3 require lifetimes of greater than 4.3 terrestrial years. For a wide range of H2O2 lifetimes, it was found that the atmospheric concentration is only weakly coupled with soil loss processes. Losses to the soil become significant only when lifetimes are less than a few hours. If there are depths below which H2O2 is not transported, it is plausible that organic compounds, protected from an oxidizing environment, may still exist. They would have been deposited by meteors, or be the organic remains of past life.
海盗号气相色谱 - 质谱仪未能在火星上检测到有机化合物,海盗号标记释放实验和海盗号气体交换实验均表明火星土壤表面具有活性。这些结果使得人们普遍认为火星土壤中存在氧化剂。由于过氧化氢是由火星大气中的光化学过程产生的,并且在实验室中已证明其能非常接近地重现海盗号标记释放实验的结果,所以它很可能是火星土壤氧化剂的候选物质。在此,我们报告火星上过氧化氢的土壤/大气耦合传输模型的结果。过氧化氢扩散到土壤中后,其浓度取决于吸附程度和催化分解速率。我们建立了一个用于计算火星大气和土壤中过氧化氢分布的分析模型。结果表明,由于非线性土壤扩散方程,土壤中过氧化氢的浓度在有限深度处降为零。该模型根据一个未知量进行参数化,即过氧化氢在土壤中非均相催化分解的寿命。将计算出的浓度与从海盗号标记释放实验推断出的30纳摩尔/立方厘米的过氧化氢浓度进行比较。该模型的一个重要结果是,对于广泛的过氧化氢寿命范围(长达10^5年),发现其灭绝深度小于3米。计算得出,在寿命大于1000年时,顶部4厘米处的最大可能浓度约为240纳摩尔/立方厘米。浓度高于30纳摩尔/立方厘米需要寿命大于4.3个地球年。对于广泛的过氧化氢寿命范围,发现大气浓度与土壤损失过程的耦合较弱。只有当寿命小于几小时时,向土壤中的损失才会变得显著。如果存在过氧化氢无法传输到的深度,那么免受氧化环境影响的有机化合物可能仍然存在。它们可能是由流星沉积的,或者是过去生命的有机残骸。