scholarly journals Heterogeneous ice nucleation correlates with bulk-like interfacial water

2019 ◽  
Vol 5 (4) ◽  
pp. eaat9825 ◽  
Author(s):  
Shuwang Wu ◽  
Zhiyuan He ◽  
Jinger Zang ◽  
Shenglin Jin ◽  
Zuowei Wang ◽  
...  

Establishing a direct correlation between interfacial water and heterogeneous ice nucleation (HIN) is essential for understanding the mechanism of ice nucleation. Here, we study the HIN efficiency on polyvinyl alcohol (PVA) surfaces with different densities of hydroxyl groups. We find that the HIN efficiency increases with the decreasing hydroxyl group density. By explicitly considering that interfacial water molecules of PVA films consist of “tightly bound water,” “bound water,” and “bulk-like water,” we reveal that bulk-like water can be correlated directly to the HIN efficiency of surfaces. As the density of hydroxyl groups decreases, bulk-like water molecules can rearrange themselves with a reduced energy barrier into ice due to the diminishing constraint by the hydroxyl groups on the PVA surface. Our study not only provides a new strategy for experimentally controlling the HIN efficiency but also gives another perspective in understanding the mechanism of ice nucleation.

2019 ◽  
Vol 72 (5) ◽  
pp. 392 ◽  
Author(s):  
Yohsuke Nikawa ◽  
Seiji Tsuzuki ◽  
Hiroyuki Ohno ◽  
Kyoko Fujita

We investigated the hydration states of cholinium phosphate-type ionic liquids (ILs) in relation to ion structure, focusing on the influence of the hydroxyl group of the cation and the alkyl chain length of the anion. Water activity measurements provided information on the macroscopic hydration states of the hydrated ILs, while NMR measurements and molecular dynamics simulations clearly showed the microscopic interactions and coordination of the water molecules. The hydrogen bonding networks in these ILs were influenced by the anion structure and water content, and the mobility of water molecules was influenced by the number of hydroxyl groups in the cation and anion.


2020 ◽  
Vol 22 (1) ◽  
pp. 258-264 ◽  
Author(s):  
Mingzhe Shao ◽  
Chuanbiao Zhang ◽  
Chonghai Qi ◽  
Chunlei Wang ◽  
Jianjun Wang ◽  
...  

Hydrogen polarity of interfacial water regulates heterogeneous ice nucleation.


2017 ◽  
Author(s):  
Donifan Barahona

Abstract. Heterogeneous ice nucleation initiated by particles immersed within droplets is likely the main pathway of ice formation in the atmosphere. Theoretical models commonly used to describe this process assume that it mimics ice formation from the vapor, neglecting interactions unique to the liquid phase. This work introduces a new approach that accounts for such interactions by linking the ability of particles to promote ice formation to the modification of the properties of water near the particle-liquid interface. It is shown that the same mechanism that lowers the thermodynamic barrier for ice nucleation also tends to decrease the mobility of water molecules, hence the ice-liquid interfacial flux. Heterogeneous ice nucleation in the liquid phase is thus determined by the competition between thermodynamic and kinetic constraints to the formation and propagation of ice. At the limit, ice nucleation may be mediated by the dynamics of vicinal water instead of the nucleation work. This new ice nucleation regime is termed spinodal ice nucleation. Comparison of predicted nucleation rates against published data suggests that some materials of atmospheric relevance may nucleate ice in this regime.


2019 ◽  
Author(s):  
Jiarun Zhou ◽  
Nurun Nahar Lata ◽  
Sapna Sarupria ◽  
will cantrell

We studied thin films of water at the mica-air interface using infrared spectroscopy and molecular dynamics simulations. We investigate the influence of ions on interfacial water by exchanging the naturally occurring K<sup>+</sup> ion with H<sup>+</sup>/Na<sup>+</sup>, Ca<sup>2+</sup>, and Mg<sup>2+</sup>. The experiments do not show a difference in the bulk structure (<i>i. e.</i> in the infrared spectra), but indicate that water is more strongly attracted to the Mg<sup>2+</sup> mica. The simulations reveal that the cation-water interactions significantly influence the microscopic arrangement of water on mica. Our results indicate that the divalent cations result in strong water-mica interactions, which leads to longer hydrogen bond lifetimes and larger hydrogen bonded clusters of interfacial water molecules. These results have implications for surface-mediated processes such as heterogeneous ice nucleation, protein assembly and catalysis.


2016 ◽  
Author(s):  
Lukas Kaufmann ◽  
Claudia Marcolli ◽  
Beiping Luo ◽  
Thomas Peter

Abstract. Homogeneous nucleation of ice in supercooled water droplets is a stochastic process. In its classical description, the growth of the ice phase requires the emergence of a critical embryo from random fluctuations of water molecules between the water bulk and ice-like clusters, which is associated with overcoming an energy barrier. For heterogeneous ice nucleation on ice-nucleating surfaces both, stochastic and deterministic descriptions are in use. Deterministic (singular) descriptions are often favored because the temperature dependence of ice nucleation on a substrate usually dominates the stochastic time dependence, and the ease of representation facilitates the incorporation in climate models. Conversely, classical nucleation theory (CNT) describes heterogeneous ice nucleation as a stochastic process with a reduced energy barrier for the formation of a critical embryo in the presence of an ice-nucleating surface. This reduction is conveniently parameterized in terms of a contact angle α between the ice phase immersed in liquid water and the heterogeneous surface area. This study investigates various ice-nucleating agents in immersion mode by subjecting them to repeated freezing cycles to elucidate and discriminate the time and temperature dependences of heterogeneous ice nucleation. Freezing rates determined from such refreeze experiments are presented for Hoggar Mountain dust, birch pollen washing water and Arizona Test Dust (ATD) and nonadecanol coatings. For the analysis of the experimental data with CNT we assumed the same active site to be always responsible for freezing. Three different CNT-based parame-terizations were used to describe rate coefficients for heterogeneous ice nucleation as a function of temperature, all leading to very similar results: for Hoggar Mountain dust, ATD and larger nonadecanol coated water droplets, the experimentally determined increase of freezing rate with decreasing temperature is too shallow to be described properly by CNT using the contact angle as the only fit parameter. Birch pollen washing water and small nonadecanol coated water droplets show the reverse behavior with temperature dependencies of freezing rates steeper than predicted by CNT formulations. Good agreement of observations and calculations can be obtained when a prefactor β is introduced to the rate coefficient as second fit parameter. Thus, the following microphysical picture emerges: Heterogeneous freezing occurs on ice-nucleating sites that need a minimum (critical) surface area to host embryos of critical size to grow into a crystal. Fits based on CNT suggest that the critical active site area is in the range of 10–50 nm2 depending on sample, temperature, and CNT-based parameterization. Two fitting parameters are needed to characterize individual active sites. The contact angle lowers the energy barrier that has to be overcome to form the critical embryo on the site compared to the homogeneous case where the critical embryo develops in the volume of water. The prefactor β is needed to adjust the calculated slope of freezing rate increase with decreasing temperature to the measured one. When it is large, there are many nucleation attempts and nucleation occurs immediately when the temperature is low enough so that the active site can accommodate a critical embryo. This is the case for active sites of birch pollen washing water and the small droplets coated with nonadecanol. If the prefactor is low, the number of nucleation attempts is low and the increase of freezing rate with decreasing temperature is shallow. This is the case for Hoggar Mountain dust, the large droplets coated with nonadecanol, and ATD. Different hypotheses why the value of the prefactor depends on the nature of the active sites are discussed.


Biophysica ◽  
2021 ◽  
Vol 1 (2) ◽  
pp. 168-178
Author(s):  
Monika Bleszynski ◽  
Matt Reil

Antifreeze glycoproteins (AFGPs) found in various fish are used by the organisms to prevent freezing. While these compounds have been studied for their ability to bind to, and prevent the complete crystallization of water, the exact mechanisms by which AFGPs prevent freezing are still undetermined. Therefore, building upon our previous work, this study uses molecular dynamics simulations to assess the effects of hydroxyl group separation distance on AFGP ice nucleation activity. Water droplet crystallization simulations showed that modified AFGP structures containing hydroxyl distances smaller than ~3.0 Å lost their ability to prevent ice crystallization. Furthermore, modified AFGP containing hydroxyl distances of 7.327 Å and 6.160 Å was correlated with a promotion in ice nucleation, as demonstrated by the changes in the energy of the system. This supports the notion that the distance, and therefore, geometry characteristics between the hydroxyl groups located on the saccharide structures play a key role in the ice crystallization inhibition properties of AFGP compounds.


2018 ◽  
Vol 233 (1) ◽  
pp. 41-49 ◽  
Author(s):  
Lukasz Dobrzycki

AbstractA new crystal structure oftert-butanol and water crystallizing as the decahydrate is reported. The crystallization of the mixture in the desired molar ratio was performed in a capillary placed directly on a goniometer of a single crystal diffractometer at 200 K and ambient pressure using focused IR laser radiation. The crystals were grown while the melting zone formed by the IR laser was moved along the capillary. Usually the crystallization process should be long enough (hours) in order to obtain a good quality single crystal. However, in the case oftert-butanol decahydrate, such a long process led to separation of the ice and alcohol. Only fast crystallization taking tens of seconds allowed crystallization of the desired crystalline phase. In the decahydratetert-butanol molecules are located in channels formed by water molecules. Hydroxyl groups are anchored to the water framework via hydrogen bonds. All water molecules in the structure have hydrogen atoms disordered equally over two sites; the hydroxyl group is likewise disordered. This effect is observed at both, 200 K and 100 K. Raman spectra recorded for the crystalline phase suggest dynamic disorder at higher temperature, converting to static at lowerT. The decahydrate oftert-butanol, together with already known itsdi- andhepta-hydrates, display similar features to those observed for series oftert-butylamine hydrates. The latter structures behave as frozen steps of amine hydration observed as crystal structures leading, at maximum dilution, to hexagonal ice. Hydrates oftert-butanol nicely follow this tendency completing the relationship found for thetert-butylamine: water system.


2017 ◽  
Vol 17 (5) ◽  
pp. 3525-3552 ◽  
Author(s):  
Lukas Kaufmann ◽  
Claudia Marcolli ◽  
Beiping Luo ◽  
Thomas Peter

Abstract. Homogeneous nucleation of ice in supercooled water droplets is a stochastic process. In its classical description, the growth of the ice phase requires the emergence of a critical embryo from random fluctuations of water molecules between the water bulk and ice-like clusters, which is associated with overcoming an energy barrier. For heterogeneous ice nucleation on ice-nucleating surfaces both stochastic and deterministic descriptions are in use. Deterministic (singular) descriptions are often favored because the temperature dependence of ice nucleation on a substrate usually dominates the stochastic time dependence, and the ease of representation facilitates the incorporation in climate models. Conversely, classical nucleation theory (CNT) describes heterogeneous ice nucleation as a stochastic process with a reduced energy barrier for the formation of a critical embryo in the presence of an ice-nucleating surface. The energy reduction is conveniently parameterized in terms of a contact angle α between the ice phase immersed in liquid water and the heterogeneous surface. This study investigates various ice-nucleating agents in immersion mode by subjecting them to repeated freezing cycles to elucidate and discriminate the time and temperature dependences of heterogeneous ice nucleation. Freezing rates determined from such refreeze experiments are presented for Hoggar Mountain dust, birch pollen washing water, Arizona test dust (ATD), and also nonadecanol coatings. For the analysis of the experimental data with CNT, we assumed the same active site to be always responsible for freezing. Three different CNT-based parameterizations were used to describe rate coefficients for heterogeneous ice nucleation as a function of temperature, all leading to very similar results: for Hoggar Mountain dust, ATD, and larger nonadecanol-coated water droplets, the experimentally determined increase in freezing rate with decreasing temperature is too shallow to be described properly by CNT using the contact angle α as the only fit parameter. Conversely, birch pollen washing water and small nonadecanol-coated water droplets show temperature dependencies of freezing rates steeper than predicted by all three CNT parameterizations. Good agreement of observations and calculations can be obtained when a pre-factor β is introduced to the rate coefficient as a second fit parameter. Thus, the following microphysical picture emerges: heterogeneous freezing occurs at ice-nucleating sites that need a minimum (critical) surface area to host embryos of critical size to grow into a crystal. Fits based on CNT suggest that the critical active site area is in the range of 10–50 nm2, with the exact value depending on sample, temperature, and CNT-based parameterization. Two fitting parameters are needed to characterize individual active sites. The contact angle α lowers the energy barrier that has to be overcome to form the critical embryo at the site compared to the homogeneous case where the critical embryo develops in the volume of water. The pre-factor β is needed to adjust the calculated slope of freezing rate increase with temperature decrease. When this slope is steep, this can be interpreted as a high frequency of nucleation attempts, so that nucleation occurs immediately when the temperature is low enough for the active site to accommodate a critical embryo. This is the case for active sites of birch pollen washing water and for small droplets coated with nonadecanol. If the pre-factor is low, the frequency of nucleation attempts is low and the increase in freezing rate with decreasing temperature is shallow. This is the case for Hoggar Mountain dust, the large droplets coated with nonadecanol, and ATD. Various hypotheses why the value of the pre-factor depends on the nature of the active sites are discussed.


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