首页> 外文期刊>Journal of Aerosol Science >Droplet evaporation and condensation in the near-continuum regime
【24h】

Droplet evaporation and condensation in the near-continuum regime

机译:近连续状态下的液滴蒸发和凝结

获取原文
获取原文并翻译 | 示例
           

摘要

The problem of quasi-steady state evaporation and condensation of aerosol droplets is re-examined to determine the effect of the molecular interaction model on the predicted mass transfer rates in the Knudsen regime. A new expression for the mass flux is obtained that contains explicitly the dependence of the rate process on the accommodation coefficient and on the molecular weight ratio of the vapor and gas molecules. The analysis, based on the solution of the Boltzmann equation by the method of Grad for Maxwellian molecules, is shown to yield results in the near-continuum regime (Kn < 1) very close to a number of previous theoretical analyses based on hard sphere molecules and semi-theoretical correlations, including the Fuchs-Sutugin equation. These results indicate that the theoretical predictions are not sensitive to the molecular interaction model used, but depend strongly on the method of solution in the near-free-molecule regime where the method of Grad fails. As the continuum regime is approached, the solution becomes independent of the accommodation coefficient. Theoretical predictions agree with previously published evaporation data for isothermal evaporation of dibutyl phthalate (DBP) in air and dibutyl sebacate (DBS) in nitrogen using an accommodation coefficient of 1.0 for DBP and 0.9 for DBS.
机译:重新检查准稳态蒸发和气溶胶液滴凝结的问题,以确定分子相互作用模型对Knudsen体制中预测的传质速率的影响。获得质量通量的新表达式,该表达式明确包含速率过程对容纳系数以及蒸汽和气体分子的分子量比的依赖性。该分析基于麦克斯韦分子的Grad方法对Boltzmann方程的求解,结果表明在近连续谱状态(Kn <1)中产生的结果非常接近先前基于硬球分子的许多理论分析和半理论相关性,包括Fuchs-Sutugin方程。这些结果表明,理论预测对所用的分子相互作用模型不敏感,但在很大程度上取决于Grad方法失败的近自由分子状态下的求解方法。随着接近连续状态,解变得独立于调节系数。理论预测与先前发布的关于空气中邻苯二甲酸二丁酯(DBP)和氮气中癸二酸二丁酯(DBS)等温蒸发的蒸发数据一致,DBP的调节系数为1.0,DBS的调节系数为0.9。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号