凝结系数 meaning in Chinese
coefficient of conde ation
coefficient of condensation
condensation coefficient
Examples
- The calculated condensation coefficients of argon from the modified theoretical formula agree well with the md simulation results from different authors . quasi - stable evaporation process of water is experimentally investigated
对于氩的凝结系数，该修正式获得的凝结系数能与本文及其他作者的模拟结果相吻合，计算准确度可望优于现有的其它凝结系数统计理论计算方法。 - From the vapor phase to the liquid phase , the temperature jumps near the interface . therefore , it is difficult to accurately measure the temperatures near the interface . this may be the main reason of the large difference between the evaporation / condensation coefficients obtained from different experiments
由于界面处存在明显的温度跳跃，界面温度的准确实验测量难度较大，这很可能是文献报道的蒸发/凝结系数的实验研究结果数据分散程度较大的主要原因。 - Further study is in < wp = 6 > demand . moreover , with a transient simulation , we calculated evaporation coefficients of argon under non - equilibrium conditions . the rudimental md results indicate that there is no notable difference between the evaporation coefficients from the non - equilibrium simulation and the condensation coefficients from the equilibrium simulation
论文还采用瞬态法研究了非平衡条件下氩的蒸发系数，模拟研究的初步结果显示，非平衡分子动力学方法获得的蒸发系数与平衡分子动力学方法获得的凝结系数之间差距并不显著，由于可比数据少，上述结果还有待于更多的模拟验证。 - With the characteristic time method , we also studied the condensation coefficients of water and argon in liquid - vapor equilibrium system . the simulated condensation coefficient decreases with the increase of temperature for both argon and water , and the condensation coefficient of water is larger than that of argon . though the polarity and the rotation are considered in the simulation of water , the difference between the condensation coefficients of water and argon is not remarkable
模拟获得的lennard - jones流体和水在平衡条件下的凝结系数表明：水和氩的凝结系数为温度的减函数；水的凝结系数略高于氩的凝结系数；虽然在水的模拟中考虑了分子的极性、旋转等因素，但模拟获得的水与氩的凝结系数之间的差距并不显著，具体原因仍有待于进一步的探讨。 - With md method , we studied evaporation and condensation process . by statistically analyzing the behavior of the colliding molecules with the interface , we presented a novel method , namely , the characteristic time method , to calculate the evaporation / condensation coefficient . in this method , the condensed then re - evaporated process is considered
对蒸发与凝结过程进行了分子动力学研究，提出了统计凝结系数的新方法- -特征时间法，该方法通过统计获得有效区分反射过程和凝结再蒸发过程的特征时间，从而使求得的凝结系数近似程度更好。