This paper presents the results of several experimental methods (FT-IR spectroscopy, UV-vis spectroscopy, fluorescence microscopy (FM), Atomic Force Microscopy (AFM)) evidencing structural changes induced in extremely diluted solutions (EDS), which are prepared by an iterated process of centesimal (1:100) dilution and succussion (shaking). The iteration is repeated until an extremely high dilution is reached, so that the composition of the solution becomes identical to that of the solvent--in this case water--used to prepare it. The experimental observations reveal the presence of supramolecular aggregates hundreds of nanometres in size in EDS at ambient pressure and temperature, and in the solid state. These findings confirm the hypothesis--developed thanks to previous physico-chemical investigations--that formation of water aggregates occurs in EDS. The experimental data can be analyzed and interpreted with reference to the thermodynamics of far-from-equilibrium systems and irreversible processes.
In the last decade, we have investigated from the physicochemical point of view, whether water prepared by the procedures of homeopathic medicine (leading inexorably to systems without any molecule different from the solvent) results in water different from the initial water? The answer, unexpectedly, but strongly supported by many experimental results is positive. We used well-established physicochemical techniques: flux calorimetry, conductometry, pHmetry and galvanic cell electrodes potential. Unexpectedly the physicochemical parameters evolve in time. The water solvent exhibits large changes in measurable physicochemical properties as a function of its history, the solute previously dissolved, and time. In particular we found evidence of two new phenomena, both totally unpredicted, in homeopathic dilutions: the presence of a maximum in the measured physicochemical parameters vs sample age, and their dependence on the volume in which the dilution is stored. These new experimental results strongly suggest the presence of an extended and 'ordered' dynamics involving liquid water molecules.
Perturbed very dilute aqueous solutions are investigated by analyzing their electric conductivity (χ). Foci include titrations and quasi-periodic oscillations of χ spanning several months. The χ data reflect persistent dissipative supramolecular self-organization. This paper's successful consistent explanations of the χ measurements corroborate earlier quantum field theoretical predictions. For example: (1) Permanent polarization results from quantum electro-dynamical interactions mediated auto-ordering of water molecules and molecular aggregates which have electric dipole moments. (2) The aggregates are created by exciting very dilute aqueous solutions, generating long lasting (cold) vortices in crystalline-like-structured super-fluidic domains. These domains are only present when the concentration (C) is lower than a solute dependent transitions concentration (C trans ). Typically, C trans is of the order of 10-4 M or below.
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