Metastable Manipulation of $H_2O$ Electronegativity via Synthetic Mineral Catalysts: The "Hidrogaring" Concept.

Authors: Shuan Nabil D.I.A
Cited by: 0

Abstract

This project introduces "Hidrogaring", a revolutionary material phase of water where adhesive properties are temporarily neutralized. By artificially inducing a spike in the electronegativity of the water molecule’s atoms toward a value of 4.0 (equivalent to Fluorine), the water loses its ability to wet surfaces (Adhesion $\approx 0$). This innovation bridges the gap between liquid dynamics and non-adhesive physics.II. Core Components & MethodologyThe Activator (Synthetic Stone): A solid-state catalyst composed of processed natural minerals (Silica/Magnesium oxides).Electrostatic Saturation: The catalyst utilizes natural electrostatic potential to saturate the Hydrogen electron cloud without the need for external electricity, preventing molecular dissociation (short-circuiting).The 10-Minute Decay Timer: The "Hidrogaring" state is designed as a metastable condition. It features a built-in 10-minute "half-life", after which the molecular configuration returns to its natural ground state ("Hidroteles" or normal wetting water).III. Applications & SafetyPractical Use: Non-wetting swimming pools, residue-free industrial cleaning, and friction-less fluid transport.Environmental Ethics: The 10-minute timer serves as a critical safety fail-safe, ensuring the water remains biocompatible for aquatic life and human consumption once it returns to its natural state.IV. Inventor’s Statement"If possible, the effect should be permanent—yet controlled." This innovation is designed to be accessible and cost-effective, utilizing minerals found globally (from Indonesia to Africa), ensuring that high-level molecular science can benefit all of humanity.

Fields of Study & Subjects

Chemical and Physical Studies Surface Modification and Superhydrophobicity Minerals Flotation and Separation Techniques

Publication details

Journal / source
OSF Preprints (OSF Preprints)
Publication date
25 January 2026
Document type
Preprint