Ren Hong-Mei, Cai Chen, Leng Chun-Bo, Pang Shu-Feng, Zhang Yun-Hong
The Institute of Chemical Physics, Key Laboratory of Cluster Science, School of Chemistry, Beijing Institute of Technology , Beijing 100081, People's Republic of China.
School of Chemistry and Molecular Engineering, East China Normal University , 500 Dongchuan Road, Shanghai 200241, People's Republic of China.
J Phys Chem B. 2016 Mar 24;120(11):2913-20. doi: 10.1021/acs.jpcb.5b12442. Epub 2016 Mar 9.
The in situ infrared spectra of sodium nitrate (NaNO3) and mixed NaNO3/glycerol droplets with organic to inorganic molar ratio (OIR) of 1:8, 1:4, 1:2, 1:1, and 2:1 on the ZnSe substrate were collected using the Fourier transform infrared attenuated total reflection (FTIR-ATR) technique in the RH linearly decreasing process. When the efflorescence process occurred in the RH decreasing process, the stochastric transformation from NaNO3 droplets to NaNO3 solid particles resulted in gradually increasing of a new band at 836 cm(-1) and contineously decreasing of an initial band at 829 cm(-1), which were assigned to the v2-NO3(-) mode in crystal phase state and in liquid state, respectively. There were excellent isobesic points between the two bands in the transformation processes, indicating the synchronization between the disappearence of NO3(-) in solutions and the production of NaNO3 crystal. The nucleation ratio, i.e., the amount of the droplets crystallized at a given RH upon the total amount droplets, was obtained by using the absorbance of ν2-NO3(-) band at 836 cm(-1), which was used to calculate the nucleation rates of NaNO3 either for heterogeneous or for homogeneous nucleation process. While the glycerol molecules delayed the efflorescence RHs (ERH) of NaNO3 in the mixed NaNO3/glycerol droplets (OIR = 2:1) to 15%, greatly lower than the ERH for pure NaNO3 droplets at 62.5%, they also greatly suppressed the heterogeneous nucleation rate with increase of the OIR ratio. Two different kinetic mechanisms were suggested in the mixed droplets with OIR = 1:8, 1:4, 1:2, and 1:1, i.e., homogeneous nucleation at higher supersaturation and heterogeneous nucleation at lower supersaturation. For the mixed droplets with 2:1 OIR, they fell into the homogeneous nucleation region completely.
在相对湿度(RH)线性下降过程中,使用傅里叶变换红外衰减全反射(FTIR - ATR)技术收集了硝酸钠(NaNO₃)以及有机与无机摩尔比(OIR)为1:8、1:4、1:2、1:1和2:1的NaNO₃/甘油混合液滴在ZnSe基底上的原位红外光谱。当在RH下降过程中发生风化过程时,从NaNO₃液滴到NaNO₃固体颗粒的随机转变导致836 cm⁻¹处新峰逐渐增强,以及829 cm⁻¹处初始峰持续减弱,这两个峰分别对应晶相状态和液相状态下的ν₂ - NO₃⁻模式。在转变过程中,这两个峰之间存在良好的等吸收点,表明溶液中NO₃⁻的消失与NaNO₃晶体的生成同步。通过使用836 cm⁻¹处ν₂ - NO₃⁻峰的吸光度获得成核率,即给定RH下结晶的液滴数量占总液滴数量的比例,该成核率用于计算异质或均质成核过程中NaNO₃的成核速率。虽然甘油分子将NaNO₃/甘油混合液滴(OIR = 2:1)中NaNO₃的风化相对湿度(ERH)延迟至15%,远低于纯NaNO₃液滴的62.5%的ERH,但随着OIR比例增加,它们也极大地抑制了异质成核速率。对于OIR = 1:8、1:4、1:2和1:1的混合液滴,提出了两种不同的动力学机制,即在较高过饱和度下的均质成核和较低过饱和度下的异质成核。对于OIR为2:1的混合液滴,它们完全落入均质成核区域。