δείτε την πρωτότυπη σελίδα τεκμηρίου στον ιστότοπο του αποθετηρίου του φορέα για περισσότερες πληροφορίες και για να δείτε όλα τα ψηφιακά αρχεία του τεκμηρίου*
Magnetic Field Trapping in Coherent Antisymmetric States of Liquid Water Molecular Rotors
Meden, A.
Riziotis, C.
Sarantopoulou, E.
Drazic, G.
Strazisar, J.
Kollia, Z.
Kobe, S.
Under external magnetic field, CaCO(3) in water solution will precipitate as aragonite than calcite, (the crystallized state at zero external magnetic field), despite that the zero field ground electronic state of aragonite is placed higher than of calcite by 28 eV. Recent experimental and theoretical results begin to elucidate the process through the amplification of a vacuum state magnetic fluctuation, which can exchange its energy with the angular momentum of a single water molecular rotor for a short period of time. The system is thus driven to a new thermodynamic state of higher free energy than the state at zero magnetic field. In the present work, is indicated that the nanocrystalization of CaCO(3) precipitants in water solution can probe the interactions between the electromagnetic field and the matter. At low external magnetic field, the formation of aragonite is taking place when a vacuum state electromagnetic mode is trapped, amplified and sustained in a coherent (collective) antisymmetric state, which is created by an ensemble of individual molecular rotors, which are excited coherently by the external magnetic field. The amplified magnetic mode will not decay to the ground symmetric state of the ensemble of water molecular rotors due to the forbidden nature of transition between the antisymmetric and the symmetric state. The ensemble of water molecular rotors is then driven to a higher free-energy state for a longer period of time, allowing thus the CaCO(3) precipitants to be crystallized as aragonite. Furthermore, the existence of the coherent antisymmetric state, elucidate the memory effects observed previously in water solutions.
*Η εύρυθμη και αδιάλειπτη λειτουργία των διαδικτυακών διευθύνσεων των συλλογών (ψηφιακό αρχείο, καρτέλα τεκμηρίου στο αποθετήριο) είναι αποκλειστική ευθύνη των αντίστοιχων Φορέων περιεχομένου.
Βοηθείστε μας να κάνουμε καλύτερο το OpenArchives.gr.
