Structure and Dynamics of Low-Density and High-Density Liquid Water at High Pressure

2013 ◽  
Vol 5 (1) ◽  
pp. 235-240 ◽  
Author(s):  
Samuele Fanetti ◽  
Andrea Lapini ◽  
Marco Pagliai ◽  
Margherita Citroni ◽  
Mariangela Di Donato ◽  
...  
2005 ◽  
Vol 123 (17) ◽  
pp. 174511 ◽  
Author(s):  
Fangfei Li ◽  
Qiliang Cui ◽  
Zhi He ◽  
Tian Cui ◽  
Jian Zhang ◽  
...  

2017 ◽  
Vol 114 (16) ◽  
pp. 4066-4071 ◽  
Author(s):  
Kentaro Nomura ◽  
Toshihiro Kaneko ◽  
Jaeil Bai ◽  
Joseph S. Francisco ◽  
Kenji Yasuoka ◽  
...  

Possible transition between two phases of supercooled liquid water, namely the low- and high-density liquid water, has been only predicted to occur below 230 K from molecular dynamics (MD) simulation. However, such a phase transition cannot be detected in the laboratory because of the so-called “no-man’s land” under deeply supercooled condition, where only crystalline ices have been observed. Here, we show MD simulation evidence that, inside an isolated carbon nanotube (CNT) with a diameter of 1.25 nm, both low- and high-density liquid water states can be detected near ambient temperature and above ambient pressure. In the temperature–pressure phase diagram, the low- and high-density liquid water phases are separated by the hexagonal ice nanotube (hINT) phase, and the melting line terminates at the isochore end point near 292 K because of the retracting melting line from 292 to 278 K. Beyond the isochore end point (292 K), low- and high-density liquid becomes indistinguishable. When the pressure is increased from 10 to 600 MPa along the 280-K isotherm, we observe that water inside the 1.25-nm-diameter CNT can undergo low-density liquid to hINT to high-density liquid reentrant first-order transitions.


2010 ◽  
Vol 150 (43-44) ◽  
pp. 2106-2108 ◽  
Author(s):  
Kai He ◽  
Duanwei He ◽  
Li Lei ◽  
Yongtao Zou ◽  
Jiaqian Qin ◽  
...  

2009 ◽  
Vol 106 (12) ◽  
pp. 4596-4600 ◽  
Author(s):  
C. U. Kim ◽  
B. Barstow ◽  
M. W. Tate ◽  
S. M. Gruner

2016 ◽  
Vol 38 ◽  
pp. 238-242 ◽  
Author(s):  
Bérengère Guignon ◽  
Eduardo Hidalgo Baltasar ◽  
Pedro D. Sanz ◽  
Valentín G. Baonza ◽  
Mercedes Taravillo

2019 ◽  
Vol 116 (19) ◽  
pp. 9191-9196 ◽  
Author(s):  
Josef N. Stern ◽  
Markus Seidl-Nigsch ◽  
Thomas Loerting

Thermal stability against crystallization upon isobaric heating at pressure 0.1 ≤ P ≤ 1.9 GPa is compared for five variants of high- (HDA) and very high-density amorphous ice (VHDA) with different preparation history. At 0.1–0.3 GPa expanded HDA (eHDA) and VHDA reach the same state before crystallization, which we infer to be the contested high-density liquid (HDL). Thus, 0.3 GPa sets the high-pressure limit for the possibility to observe HDL for timescales of minutes, hours, and longer. At P > 0.3 GPa the annealed amorphous ices no longer reach the same state before crystallization. Further examination of the results demonstrates that crystallization times are significantly affected both by the density of the amorphous matrix at the crystallization temperature Tx as well as by nanocrystalline domains remaining in unannealed HDA (uHDA) as a consequence of incomplete pressure-induced amorphization.


Author(s):  
L. Mulestagno ◽  
J.C. Holzer ◽  
P. Fraundorf

Due to the wealth of information, both analytical and structural that can be obtained from it TEM always has been a favorite tool for the analysis of process-induced defects in semiconductor wafers. The only major disadvantage has always been, that the volume under study in the TEM is relatively small, making it difficult to locate low density defects, and sample preparation is a somewhat lengthy procedure. This problem has been somewhat alleviated by the availability of efficient low angle milling.Using a PIPS® variable angle ion -mill, manufactured by Gatan, we have been consistently obtaining planar specimens with a high quality thin area in excess of 5 × 104 μm2 in about half an hour (milling time), which has made it possible to locate defects at lower densities, or, for defects of relatively high density, obtain information which is statistically more significant (table 1).


1975 ◽  
Vol 33 (02) ◽  
pp. 256-270
Author(s):  
R. M Howell ◽  
S. L. M Deacon

SummaryElectron microscopy and particle electrophoresis were found to be complementary techniques with which to complete the physical data from an earlier study on barium sulphates used to adsorb clotting factors from serum. The differences revealed by scanning electron microscopy (S. E. M.) in the physical shape of low and high density grades of barium sulphate particles appear to be of greater significance than charge as expressed by electrophoretic mobility, in determining whether or not precursor or preformed factor Xa is eluted.This conclusion was based on the finding that at pH values close to 7, where the adsorption from serum occurs, all samples with the exception of natural barytes were uncharged. However as the high-density, or soil-grade, was found by S. E. M. to consist of large solid crystals it was suggested that this shape might induce activation of factor X as a result of partial denaturation and consequent unfolding of the adsorbed protein. In contrast, uptake of protein into the centre of the porous aggregates revealed by S. E. M. pictures of low-density or X-ray grade barium sulphate may afford protection against denaturation and exposure of the enzyme site.The porous nature of particles of low-density barium sulphate compared with the solid crystalline forms of other grades accounts not only for its lower bulk density but also for its greater surface/gram ratio which is reflected by an ability to adsorb more protein from serum.Neither technique produced evidence from any of the samples to indicate the presence of stabilising agents sometimes used to coat particles in barium meals.


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