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Revision 4235 by plouden, Mon Dec 8 18:31:51 2014 UTC vs.
Revision 4236 by plouden, Mon Dec 8 19:12:33 2014 UTC

# Line 65 | Line 65 | hydrophilic than the prismatic and secondary prismatic
65  
66   %\abbreviations{QLL, quasi liquid layer; MD, molecular dynamics}
67  
68 < %\dropcap{I}n this article we study the evolution of ``almost-sharp'' fronts
69 < %for the surface quasi-geostrophic equation. This 2-D active scalar
70 < %equation reads for the surface quasi-geostrophic equation.
71 < %\begin{equation}
72 < %\mfrac{D \theta}{Dt}=\mfrac{\pr \theta}{\pr t} + u\cdot \nabla
73 < %\theta=0 \label{qg1}
74 < %\end{equation}
75 <
76 < The Ice-I$_\mathrm{h}$/water quiescent interface has been extensively studied
68 > \dropcap{T}he Ice-I$_\mathrm{h}$/water quiescent interface has been extensively studied
69   over the past 30 years by theory and experiment. Haymet \emph{et al.} have
70   done significant work characterizing and quantifying the width of these
71   interfaces for the SPC,\cite{Karim90} SPC/E,\cite{Gay02,Bryk02},
# Line 119 | Line 111 | interfacial temperature\cite{Kuang12}.
111   non-equilibrium molecular dynamics (VSS-RNEMD), simultaneous temperature and
112   velocity gradients were applied to the system, allowing for measurment
113   of friction and thermal transport properties while maintaining a stable
114 < interfacial temperature\cite{Kuang12}.
114 > interfacial temperature\cite{Kuang12}. The resulting solid/liquid kinetic friction coefficients were
115 > reported, and displayed a factor of two difference between the
116 > basal and prismatic facets. We beleived this was due to an effective
117 > difference in the contact of the water with the different facets.
118  
119 < Paragraph here about hydrophobicity and hydrophilicity, maybe move up
120 < more in the paper as well. Talk about physically what it means for a
121 < surface to by hydrophobic or hydrophilic, and then we move into
122 < how do we define it (mathematically) and then measure the degree
123 < of wetting experimentally and theoretically.
119 > Surfaces exhibit varying interactions with water, and are
120 > charactarized as either being hydrophobic or hydrophilic based on the
121 > extent of these interactions. Hydrophobic surfaces have unfavorable
122 > solid-liquid interactions, and result in water maintaining a spherical
123 > or droplet shape on the surface. This occurs due to the liquid-liquid
124 > intermolecular forces being stronger than the solid-liquid
125 > interaction. Conversely, hydrophilic surfaces display large water
126 > spreading over the surface. Here solid-liquid interactions are
127 > stronger than the liquid-liquid interactions, which results in the
128 > water spreading out over the surface.
129  
130   The hydrophobicity or hydrophilicity of a surface can be described by the
131   extent a droplet of water wets the surface. The contact angle formed between
# Line 149 | Line 149 | The resulting solid/liquid kinetic friction coefficien
149   the change in contact angle to be due to the external field perturbing the
150   hydrogen bonding of the liquid/vapor interface\cite{Daub07}.
151  
152 The resulting solid/liquid kinetic friction coefficients were
153 reported, and displayed a factor of two difference between the
154 basal and prismatic facets.
152   In this paper we present the same analysis for the pyramidal and secondary
153   prismatic facets, and show that the differential interfacial friction
154   coefficients for the four facets of ice-I$_\mathrm{h}$ are determined by their
# Line 306 | Line 303 | by shearing the ice through water.
303   These results indicate that the surface structure of the exposed ice crystal
304   has little to no effect on how far into the bulk the ice-like structural
305   ordering is. Also, it appears that the interface is not structurally effected
306 < by shearing the ice through water.
306 > by the movement of water over the ice.
307  
308  
309   \subsection{Orientational dynamics}

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