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10.1038/srep32040 http://scihub22266oqcxt.onion/10.1038/srep32040 C5000010!5000010!27562476     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Sci+Rep 2016 ; 6 (ä): ä Nephropedia Template TP {{tp|p=27562476|t=2016. Ice VII from aqueous salt solutions: From a glass to a crystal with broken H-bonds |pdf=|usr=}}{{27562476}} gab.com Text Ice VII from aqueous salt solutions: From a glass to a crystal with broken H-bonds JO: Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=27562476 #FOAvip It has been known for decades that certain aqueous salt solutions of LiCl and LiBr readily form glasses when cooled to below ?160?K. This fact has recently been exploited to produce a « salty » high-pressure ice form: When the glass is compressed at low temperatures to pressures higher than 4?GPa and subsequently warmed, it crystallizes into ice VII with the ionic species trapped inside the ice lattice. Here we report the extreme limit of salt incorporation into ice VII, using high pressure neutron diffraction and molecular dynamics simulations. We show that high-pressure crystallisation of aqueous solutions of LiCl?RH2O and LiBr?RH2O with R?=?5.6 leads to solids with strongly expanded volume, a destruction of the hydrogen-bond network with an isotropic distribution of water-dipole moments, as well as a crystal-to-amorphous transition on decompression. This highly unusual behaviour constitutes an interesting pathway from a glass to a crystal where translational periodicity is restored but the rotational degrees of freedom remaining completely random. Twit Text FOAVip Ice VII from aqueous salt solutions: From a glass to a crystal with broken H-bonds ????Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=27562476 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27562476 #FOAvip English Wikipedia <ref>{{Cite pmid|27562476}}</ref> Ice VII from aqueous salt solutions: From a glass to a crystal with broken H-bonds #MMPMID27562476 Klotz S; Komatsu K; Pietrucci F; Kagi H; Ludl AA; Machida S; Hattori T; Sano-Furukawa A; Bove LE Sci Rep 2016[]; 6 (ä): ä PMID27562476show ga It has been known for decades that certain aqueous salt solutions of LiCl and LiBr readily form glasses when cooled to below ?160?K. This fact has recently been exploited to produce a « salty » high-pressure ice form: When the glass is compressed at low temperatures to pressures higher than 4?GPa and subsequently warmed, it crystallizes into ice VII with the ionic species trapped inside the ice lattice. Here we report the extreme limit of salt incorporation into ice VII, using high pressure neutron diffraction and molecular dynamics simulations. We show that high-pressure crystallisation of aqueous solutions of LiCl?RH2O and LiBr?RH2O with R?=?5.6 leads to solids with strongly expanded volume, a destruction of the hydrogen-bond network with an isotropic distribution of water-dipole moments, as well as a crystal-to-amorphous transition on decompression. This highly unusual behaviour constitutes an interesting pathway from a glass to a crystal where translational periodicity is restored but the rotational degrees of freedom remaining completely random. äIce VII from aqueous salt solutions: From a glass to a crystal with br(epmc).pdf DeepDyve Pubget Overpricing