Abstract
Liquid water is thought by many to be composed of a quasi-stable mixture of clusters that range in size from dimers to several hundred molecules and even to micrometer-size units [1–3]. The implications of such a three-dimensional structure, or whether it even exists, are often subject to debate. While many treatments (temperature change, shaking, electro-magnetic radiation, etc.) alter the physical-chemical properties of water, just how these interventions may affect the assemblage of clusters is often a matter of conjecture. The object of this study is to relate the effect of a weak, spinning, magnetic field to the assemblage of water clusters, and the subsequent changes in the chemical reactivity of bulk water. The results show that such a weak, rotating, magnetic field applied to water can either increase or decrease the spontaneous net rate of hydration of CO2, depending on the direction of spin of the magnet and the history of a given water sample. The targets for a magnetic field applied in this way are chiral water clusters and their destruction, or the inter/intra-conversion of enantiomers, can change the reactivity of water. The conclusion is that samples of distilled water, under otherwise identical conditions, can have a range of chemical reactivities depending on their individual assemblage of clusters.
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ACKNOWLEDGMENTS
The author would like to thank William Lucas and Savithramma Dinesh-Kumar, Chairs of the Plant Biology Department, for their support and encouragement, and Paul Jursinic for detailed reading of the manuscript and useful commentary.
Funding
Research support was provided by the University of California-Davis, Department of Plant Biology. No extramural funding was received.
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Stemler, A.J. Rotational Direction of a Weak Magnetic Field Selectively Targets Chiral Clusters in Liquid Water and Modifies Its Chemical Reactivity. J. Water Chem. Technol. 45, 544–551 (2023). https://doi.org/10.3103/S1063455X23060115
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DOI: https://doi.org/10.3103/S1063455X23060115