A hydrogen ion-rich electron active water device

Abstract

The application provides a hydrogen ion-rich electron active water device, relates to the hydrogen ion-rich electron active water preparation technical field, and comprises an electrolytic cell, a resonant circuit unit, a permanent magnet unit, a resonant cavity, an ultrasonic generator, a nano bubble stabilizing layer, a far infrared radiation plate, a tunable microwave generator and a controller. The parallel titanium-based platinum-plated electrodes in the electrolytic cell are matched with the resonant circuit, the electrolysis efficiency is optimized to generate hydrogen ions, the permanent magnet unit on the outer wall of the electrolytic cell forms a vertical magnetic field, and the electrolysis is assisted to improve the electron activity. The resonant cavity is connected with a water outlet, the ultrasonic generator at the bottom is matched with the inner wall nano bubble stabilizing layer, nano bubbles are generated and stabilized to enhance the water activity, the far infrared radiation plate outside the water outlet pipeline and the downstream tunable microwave generator improve the water structural properties, the controller starts the microwave generator after the ultrasonic generator stops running for a preset period of time, the microwave power is increased when the ultrasonic generator runs for more than the preset time length, the processing effect is dynamically optimized, and the hydrogen ion-rich high-activity electron water is prepared.

Description

Technical Field

[0001] This invention relates to the field of hydrogen-rich ion-active water preparation technology, and in particular to a hydrogen-rich ion-active water device. Background Technology

[0002] Existing water electrolysis technologies typically rely on a single electrolysis process to produce hydrogen-containing water. This process has limited efficiency, and the generated hydrogen molecules tend to aggregate into large bubbles that quickly dissipate, resulting in low dissolved hydrogen concentrations, poor stability, and short-lived activity. Conventional electrode structures (such as non-porous or ordinary coated electrodes) have insufficient effective reaction area, limiting ion exchange efficiency and hydrogen production rates.

[0003] Meanwhile, the lack of effective intervention in the water molecule cluster structure limits the improvement of water activity. Although magnetic field-assisted electrolysis can optimize ion migration, static or non-uniform magnetic field layouts cannot fully coordinate the electrolysis reaction. In addition, traditional systems lack sufficient control over bubble size and stability, making it difficult for nanoscale active hydrogen to persist in water.

[0004] In terms of energy field synergy, existing technologies often utilize energy forms such as ultrasound, microwaves, or far-infrared in isolation, lacking precise timing and frequency matching. For example, active sites generated by ultrasonic cavitation effects will rapidly decay if not utilized in time, while microwave energy, if out of sync with ultrasonic frequencies, will not only fail to synergize but may also interfere with the resonant state of water molecules. The lack of system control strategies leads to conflict risks during multi-energy field operation (such as overheating caused by simultaneous operation) and the inability to dynamically adjust parameters (such as microwave power) according to real-time operating conditions, resulting in energy waste or fluctuating effects. Summary of the Invention

[0005] In view of this, the technical problem to be solved by the present invention is: how to provide a hydrogen-rich ion-active water device to achieve efficient preparation of hydrogen-rich ion-active water.

[0006] To achieve the above objectives, this invention proposes a hydrogen-rich ion-active water device, comprising an electrolyzer, a resonant circuit unit, a permanent magnet unit, a resonant cavity, an ultrasonic generator, a nanobubble stabilizing layer, a far-infrared radiation plate, a tunable microwave generator, and a controller.

[0007] The electrolytic cell is provided with at least one pair of titanium-based platinum-plated electrodes arranged in parallel. The spacing between the titanium-based platinum-plated electrodes ranges from 3m to 8mm. The resonant circuit unit consists of an adjustable inductor and a capacitor. The resonant circuit unit is electrically connected to the titanium-based platinum-plated electrodes.

[0008] The permanent magnet units are arranged in a rectangular array on the outer wall of the electrolytic cell, and the magnetic field generated by the permanent magnet units is perpendicular to the plane of the titanium-based platinum-plated electrode.

[0009] The resonant cavity is connected to the outlet of the electrolytic cell, the ultrasonic generator is connected to the bottom of the resonant cavity, and the nanobubble stabilizing layer is composed of silica nanotubes arranged in a rectangular array and is attached to the inner wall of the resonant cavity.

[0010] The far-infrared radiation plate is made of ceramic material doped with rare earth elements. The far-infrared radiation plate covers the outer surface of the water outlet pipe, which is connected to the water outlet. The tunable microwave generator is installed downstream of the far-infrared radiation plate.

[0011] Furthermore, the surface of the titanium-based platinum-plated electrode is provided with a porous structure, the pore size of which is 5μm-20μm and the porosity of which is 30%-60%.

[0012] Furthermore, the permanent magnet unit is composed of alternating neodymium iron boron magnets and ferrite magnets, and the spacing between adjacent neodymium iron boron magnets and ferrite magnets is 1 / 5 to 1 / 3 of the length of the titanium-based platinum-plated electrode.

[0013] Furthermore, the operating frequency of the ultrasonic generator is defined as f. u The operating frequency of the tunable microwave generator is defined as f. m ;

[0014] Among them, f m =α×f u The f u The value range of α is 28kHz-100kHz, and the value range of α is 1.1-1.3.

[0015] Furthermore, the controller is configured to drive the tunable microwave generator to start operation again after a preset time delay when the ultrasonic generator stops operating.

[0016] Furthermore, the controller is configured to increase the operating power of the tunable microwave generator when the operating time of the ultrasonic generator exceeds a preset time.

[0017] Furthermore, the controller is configured to increase the operating power of the tunable microwave generator, specifically including:

[0018] P m =P0×[1+0.05×(T)] u -T0) / T0], where P m P0 represents the increased operating power of the tunable microwave generator, and T represents the reference power of the tunable microwave generator. uT0 is the operating time of the ultrasonic generator, and T0 is the preset time.

[0019] Furthermore, the preset time period is 5s-8s.

[0020] Compared with related technologies, the hydrogen-rich ion-active water device proposed in this invention has the following advantages:

[0021] (1) The titanium-based platinum-plated electrodes arranged in parallel in the electrolytic cell, combined with the resonant circuit unit composed of adjustable inductors and capacitors, can optimize the electrolysis efficiency and facilitate the generation of hydrogen ions. The permanent magnet unit is arranged in a rectangular array on the outer wall of the electrolytic cell. It is composed of alternating neodymium iron boron magnets and ferrite magnets, forming a magnetic field perpendicular to the electrode plane, which can assist the electrolysis process and enhance electronic activity.

[0022] (2) The resonant cavity is connected to the outlet of the electrolytic cell, and the ultrasonic generator at the bottom operates at a frequency f. u At 28kHz-100kHz, a nanobubble stabilizing layer composed of a rectangular array of silica nanotubes is attached to the inner wall, which can generate and stabilize nanobubbles and enhance the activity of water.

[0023] (3) The far-infrared radiation plate covering the outer surface of the water outlet pipe is made of ceramic material doped with rare earth elements. The tunable microwave generator downstream of it can further improve the structure and properties of the water. The tunable microwave generator is started 5-8 seconds after the ultrasonic generator stops running to avoid interference. When the ultrasonic generator runs for longer than the preset time T0, the working power of the tunable microwave generator is increased to dynamically optimize the treatment effect and ensure that the device operates efficiently and stably, thereby producing hydrogen-rich, highly active electronic water. Attached Figure Description

[0024] Figure 1 This is a schematic diagram of the structure of a hydrogen-rich ion-active water device according to an embodiment of the present invention;

[0025] Figure 2 This is an electrical connection diagram of a hydrogen-rich ion-active water device according to an embodiment of the present invention;

[0026] Figure 3 This is an electrical connection diagram of a hydrogen-rich ion-active water device according to an embodiment of the present invention. Detailed Implementation

[0027] The present invention will now be described in further detail with reference to the accompanying drawings and specific embodiments.

[0028] Please see Figures 1-3As shown, the present invention proposes a hydrogen-rich ion-active water device, including an electrolytic cell 11, a resonant circuit unit 12, a permanent magnet unit 13, a resonant cavity 14, an ultrasonic generator 15, a nanobubble stabilizing layer 16, a far-infrared radiation plate 17, a tunable microwave generator 18, and a controller 19.

[0029] The electrolytic cell 11 is provided with at least one pair of titanium-based platinum-plated electrodes 111 arranged in parallel. The spacing between the titanium-based platinum-plated electrodes 111 is 3mm-8mm. The resonant circuit unit 12 consists of an adjustable inductor and a capacitor. The resonant circuit unit 12 is electrically connected to the titanium-based platinum-plated electrodes.

[0030] The surface of the titanium-based platinum-plated electrode 111 has a porous structure with a pore size of 5μm-20μm and a porosity of 30%-60%. The electrodes are arranged in parallel with a spacing strictly limited to a specific range. This design ensures a uniformly distributed electric field gradient within the electrolytic cell 11, effectively avoiding polarization caused by excessively high local current density, while providing an optimized migration channel for charged particles.

[0031] The electrode substrate is made of titanium metal, and its surface plating gives the electrode excellent electrocatalytic activity and chemical inertness. This significantly reduces the overpotential of the hydrolysis reaction and can withstand the strong oxidizing environment generated during electrolysis, ensuring the long-term stability of the electrode. In particular, the porous microstructure constructed on the electrode surface significantly increases the effective electrochemical reaction area, fundamentally improving the dissociation efficiency of water molecules at the electrode interface. These microporous structures also serve as preferential nucleation sites for hydrogen bubbles, which is beneficial for controlling the size and distribution of the generated bubbles. This characteristic forms a key link with the subsequent ultrasonic fragmentation process, creating favorable conditions for generating micron-sized initial bubbles suitable for the treatment of the nanobubble stabilization layer 16.

[0032] The electrode achieves dynamic frequency tuning through resonant circuit unit 12, enabling it to synergize with the vertical magnetic field generated by permanent magnet unit 13. The Lorentz force under the magnetic field can directionally guide the migration trajectory of hydrogen ions generated by electrolysis, reducing disordered collision losses during ion migration.

[0033] The permanent magnet units 13 are arranged in a rectangular array on the outer wall of the electrolytic cell 11, and the magnetic field generated by the permanent magnet units 13 is perpendicular to the plane of the titanium-based platinum-plated electrode. The permanent magnet units 13 are composed of alternating neodymium iron boron magnets and ferrite magnets, and the spacing between adjacent neodymium iron boron magnets and ferrite magnets is 1 / 5 to 1 / 3 of the length of the titanium-based platinum-plated electrode.

[0034] The permanent magnet units 13 are arranged in a rectangular array on the outer wall of the electrolytic cell 11, with the magnetic field direction strictly perpendicular to the plane of the internal titanium-based platinum-plated electrode. This directional magnetic field layout mainly affects the migration behavior of charged particles during electrolysis: under the action of a DC electric field, hydrogen ions and hydroxide ions generated by water electrolysis are deflected by Lorentz force along the magnetic field direction, forming a spiral trajectory, thereby significantly increasing the residence time of ions in the electrode region. This effect, on the one hand, increases the effective collision probability between ions and the electrode surface, enhancing electrolysis efficiency; on the other hand, it slows down the adhesion speed of bubbles on the electrode surface, inhibiting the formation of large-sized bubble clusters.

[0035] The permanent magnet unit 13 employs an alternating arrangement of neodymium iron boron (NdFeB) and ferrite magnets. This hybrid configuration, through the spatial combination of materials with different magnetic permeabilities, creates a gradient magnetic field strength distribution in the electrolysis region. Specifically, the NdFeB magnets provide a high-intensity static magnetic field to ensure the fundamental Lorentz force effect; the ferrite magnets, through magnetic flux conduction, regulate the magnetic field strength of adjacent electrode regions, resulting in a smooth transition. This design avoids ion movement hindrance caused by excessively strong local magnetic fields and eliminates reaction blind zones in weak magnetic field areas, thereby improving the overall reaction uniformity within the electrolyzer 11. The vertical magnetic field guides the diffusion path of electrolysis byproducts (such as hydroxyl radicals), reducing the deposition rate of the passivation layer on the electrode surface, thus maintaining the long-term stability of the electrode active surface and providing a continuous and efficient supply of electrolysis products for subsequent water treatment processes.

[0036] The resonant cavity 14 is connected to the outlet 21 of the electrolytic cell 11, the ultrasonic generator 15 is connected to the bottom of the resonant cavity 14, and the nanobubble stabilizing layer 16 is composed of silica nanotubes arranged in a rectangular array. The nanobubble stabilizing layer 16 is attached to the inner wall of the resonant cavity 14.

[0037] The resonant cavity 14 is connected to the outlet 21 of the electrolytic cell 11, and its main function is to amplify the acoustic energy effect through a specific geometric structure. This cavity is designed to acoustically match the ultrasonic generator 15. When the ultrasonic generator 15 operates, a standing wave field is formed within the cavity, subjecting the primary hydrogen bubbles in the hydrogen-containing aqueous solution output from the electrolytic cell 11 to periodic compression and expansion. This high-frequency pressure oscillation induces the violent collapse of cavitation nuclei, generating localized high-pressure shock waves, thereby breaking millimeter-sized bubbles into a submicron-sized dispersion system, creating the foundation for subsequent nano-scale processing.

[0038] A nanobubble stabilizing layer 16 is attached to the inner wall of the resonant cavity 14, and its core is composed of a rectangular array of silica nanotubes. This structure captures the microbubbles flowing through the resonant cavity 14 through the capillary force of the nanoscale channels, forcing the bubbles to undergo morphological reconstruction under the constraint of the tube diameter. The negative charge carried on the tube wall surface forms a double-layer repulsive barrier with the hydrogen bubble interface, effectively preventing the aggregation of adjacent bubbles. This synergistic effect of physical confinement and electrostatic stabilization ensures that the hydrogen bubble size is stably maintained at the nanoscale, overcoming the inherent defect of rapid gas escape in traditional hydrogen dissolution technology.

[0039] The resonant cavity 14 first utilizes ultrasonic cavitation to achieve initial bubble refinement, and then the nanobubble stabilization layer 16 achieves size locking through interface engineering. This staged treatment mode avoids excessive fragmentation or uncontrolled thermal effects caused by a single energy input, while ensuring that the nano-hydrogen bubbles possess sufficient interfacial activity. In hydrogen-containing water treated in this process, hydrogen molecules enter the subsequent far-infrared radiation and microwave excitation stages in a highly dispersed state, significantly enhancing the reactivity and half-life of hydrogen ions in functionalized water.

[0040] The far-infrared radiation plate 17 is made of ceramic material doped with rare earth elements. The far-infrared radiation plate 17 covers the outer surface of the water outlet pipe 22, which is connected to the water outlet 21. The tunable microwave generator 18 is installed downstream of the far-infrared radiation plate 17.

[0041] The far-infrared radiating plate 17 is disposed on the outer surface of the water outlet pipe 22. Its main function is to reconstruct the molecular structure of water through electromagnetic radiation in a specific wavelength band. This radiating plate is made of rare-earth element-doped ceramic material. When water flows through the covered area, the material is heated and continuously releases far-infrared rays with wavelengths concentrated in the 8-14 μm range. This wavelength band resonates with the inherent vibrational frequency of water molecules, causing a directional weakening of the hydrogen bond network between water molecules. This energy transfer effect effectively dissociates the tightly connected state of traditional water molecule clusters, reorganizing the large molecular cluster structure into discrete units with low polymerization degree, creating favorable conditions for subsequent active penetration of hydrogen ions.

[0042] This device plays a crucial role in molecular-scale activation within the overall process chain. After being treated by the resonant cavity 14 and the nanobubble stabilizing layer 16, the hydrogen-containing water stream enters the far-infrared region. The radiant energy first acts on the outer electron cloud of the water molecules, increasing the molecular kinetic energy by enhancing the probability of electron transitions. Simultaneously, the nanobubbles generate surface plasmon resonance in the infrared radiation field, significantly reducing the interfacial tension of the bubbles and accelerating the dissolution and permeation of hydrogen into the water phase. This dual mechanism jointly promotes the binding efficiency of hydrogen ions and small water molecule clusters.

[0043] The far-infrared radiating plate 17 and the tunable microwave generator 18 form a progressive energy field relationship. After the radiating plate completes the basic molecular structure adjustment, the water already possesses an optimized energy absorption threshold before entering the microwave excitation region. In particular, the far-infrared pretreatment reduces the rotational inertia of water molecules, allowing subsequent microwave frequencies to excite the dipole resonance of hydrogen ions at lower energy inputs. This synergistic design avoids molecular structure damage caused by a single high-frequency energy source while ensuring the continuity of energy transfer throughout the activation process, ultimately forming an ion-electron active water system with a stable reduction potential.

[0044] An ultrasonic generator 15 is located at the bottom of the resonant cavity 14, and its main function is to induce cavitation in the water through high-frequency mechanical vibration. When the generator is working, the sound wave energy of a specific frequency forms a periodic pressure oscillation field within the cavity, causing a large number of transient cavitation nuclei to be generated in the hydrogen-containing aqueous solution flowing through this area. These cavitation nuclei violently collapse under the action of sound pressure, generating local high-pressure shock waves and microjets, effectively breaking up the primary hydrogen bubbles generated by electrolysis and reducing their size to a submicron-scale dispersion system. This process significantly increases the specific surface area of ​​the gas-liquid interface, laying the physical foundation for subsequent nanoscale stabilization treatment.

[0045] A tunable microwave generator 18 is installed downstream of the far-infrared radiating plate 17. Its core function is to excite a directional resonance response in water molecules. The output frequency of this device is precisely matched to the rotational energy level transition threshold of water molecules, causing the pre-treated small molecule clusters and dissolved hydrogen ions to generate high-frequency dipole oscillations. This resonance effect endows hydrogen ions with additional kinetic energy, promoting their penetration of the hydrogen bond steric hindrance between water molecules and forming a highly reactive hydrated hydrogen ion complex structure. At the same time, the microwave field polarizes the double layer of the nanobubble interface, enhancing the dissolution and permeation efficiency of hydrogen molecules into the aqueous phase.

[0046] The two devices operate in a time-sequential coordinated manner via controller 19. The control system, according to a preset program, delays the start of the microwave generator for a specific period after the ultrasonic waves cease operation, ensuring that the cavitation bubbles undergo nano-stabilization before receiving electromagnetic excitation. The microwave operating frequency is correlated with the ultrasonic frequency in a fixed ratio, creating a closed-loop energy transfer mechanism between molecular-scale vibrational energy and macroscopic cavitation effects. The power adaptive module dynamically adjusts the microwave output intensity based on changes in the ultrasonic operation duration, compensating for thermodynamic losses caused by water temperature rise and maintaining the energy balance of the activation reaction. This coordinated mechanism avoids energy field interference effects, achieving simultaneous optimization of hydrogen ion activity and stability.

[0047] Define the operating frequency of ultrasonic generator 15 as f u The operating frequency of the tunable microwave generator 18 is defined as f. m , where f m =α×f u . Specifically, f uThe value range of is 28kHz-100kHz, and the value range of α is 1.1-1.3. This frequency correlation mechanism achieves optimal coupling for energy transfer through spectrum matching. The ultrasonic generator 15 operates within a set frequency range, inducing cavitation effects in the resonant cavity 14 to form a microbubble interface; the tunable microwave generator 18 follows a fixed proportional coefficient, ensuring that its output frequency precisely corresponds to a specific multiple of the ultrasonic frequency. When the microwave frequency is slightly higher than the ultrasonic fundamental frequency, its electromagnetic wave period and the interface oscillation period generated by the collapse of cavitation bubbles form a time phase match. This matching allows the microwave electric field to act on the newly formed interface exposed at the moment of bubble collapse, enhancing the efficiency of hydrogen ion transfer from the gas phase to the liquid phase. At the same time, this proportional range can avoid the standing wave superposition effect, preventing specific frequency combinations from forming energy stagnation points in the pipe, leading to local overheating.

[0048] The controller 19 is configured to delay the start of the tunable microwave generator 18 for a preset time period (5-8 seconds) after the ultrasonic generator 15 stops operating. This control feature achieves a physical synergistic effect of the energy field through timing optimization. When the ultrasonic generator 15 stops operating, the control system automatically delays the start of the tunable microwave generator 18 for a specific period. This design mainly addresses the dynamic connection problem between residual cavitation effect and electromagnetic excitation: at the instant the ultrasonic wave stops, a large number of unstable cavitation nuclei and high-frequency pressure oscillation waves still exist in the resonant cavity 14. If microwave energy is applied immediately, the sound pressure field and the electromagnetic field will interfere with each other, weakening the energy transfer efficiency.

[0049] The delay period allows the water to complete the necessary physical relaxation process. Within the preset time period, the nanobubble stabilizing layer 16 continuously exerts capillary adsorption, promoting the full embedding of submicron bubbles generated by cavitation breakup into the silica nanotube array. Simultaneously, water molecules naturally transition from high-frequency mechanical vibration modes to the ground state energy level, establishing a stable molecular orientation basis for subsequent electromagnetic resonance. This buffering mechanism ensures that when the water flows into the microwave interaction region, the charge distribution at the hydrogen bubble interface and the dipole moment direction of the water molecules both reach a controllable excitation state. This time period setting is implicitly related to the system frequency parameters. Since there is a fixed proportional relationship between the ultrasonic operating frequency and the microwave frequency, the delay duration must cover the complete cycle of acoustic energy decay to the background noise level. Within this cycle, the nanobubbles complete the dynamic equilibrium process of surface tension, making the subsequent polarization effect of the microwave field on the bubble double layer more uniform.

[0050] The controller 19, through precise timing management, avoids energy dissipation caused by the superposition of multiple physical fields, and ensures a seamless transition of hydrogen ions from mechanical breakage to electromagnetic activation, ultimately achieving continuous enhancement of the electronic state of hydrogen ions in the active water.

[0051] Controller 19 is configured to increase the operating power of tunable microwave generator 18 when the operating time of ultrasonic generator 15 exceeds a preset time. The formula for calculating the increased operating power of tunable microwave generator 18 is: P m =P0×[1+0.05×(T)] u -T0) / T0];where P m P0 represents the increased operating power of the tunable microwave generator 18, and T represents the reference power of the tunable microwave generator 18. u T0 is the operating time of the ultrasonic generator 15, and T0 is the preset time.

[0052] This control feature maintains the thermodynamic balance of the water activation process through a dynamic power compensation mechanism. When the ultrasonic generator 15 operates continuously for more than a preset time threshold, the heat accumulation caused by cavitation in the water leads to an increase in molecular kinetic energy. At this time, maintaining the microwave generator's reference power would weaken the resonant energy transfer efficiency. The control system monitors the ultrasonic operating time parameter in real time and automatically triggers the power adjustment algorithm after reaching the preset critical value, so that the microwave output intensity increases proportionally with the extension of the ultrasonic operating time.

[0053] This regulation mechanism is based on the principle of compensating for the heat dissipation of water molecule energy level transitions. As the water temperature rises, the binding energy threshold between hydrogen ions and water molecules increases accordingly, and the microwave field strength at the original reference power is insufficient to excite effective dipole resonance. The power enhancement module converts the variable of ultrasonic working time into an increment of microwave power through a specific proportional coefficient, ensuring that the microwave energy penetration depth always covers the core region of the water flow. This design ensures that the vibrational energy acquired by hydrogen ions increases synchronously with the intensity of thermal motion in the water, avoiding the attenuation of the activation effect due to changes in the thermodynamic environment.

[0054] This function works in conjunction with the system protection mechanism. The power increase limit is dynamically limited by the controller 19 based on thermal sensor data to prevent excessive microwave power from causing localized overheating. At the same time, the microwave frequency strictly adheres to the proportional relationship with the ultrasonic frequency to maintain precise matching of molecular resonance. This intelligent power adaptation strategy not only ensures activation stability under long-term operating conditions but also optimizes system energy efficiency through refined control of energy input, ultimately ensuring that the ion activity of the produced water remains at a constant standard.

[0055] Finally, it should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention, and not to limit them; although the present invention has been described in detail with reference to the foregoing embodiments, those skilled in the art should understand that modifications can still be made to the technical solutions described in the foregoing embodiments, or equivalent substitutions can be made to some of the technical features; and these modifications or substitutions do not cause the essence of the corresponding technical solutions to deviate from the spirit and scope of the technical solutions of the embodiments of the present invention.

Claims

1. A hydrogen-rich ion-active water device, characterized in that, It includes an electrolytic cell, a resonant circuit unit, a permanent magnet unit, a resonant cavity, an ultrasonic generator, a nanobubble stabilizing layer, a far-infrared radiation plate, a tunable microwave generator, and a controller. The electrolytic cell is provided with at least one pair of titanium-based platinum-plated electrodes arranged in parallel. The spacing between the titanium-based platinum-plated electrodes ranges from 3m to 8mm. The resonant circuit unit consists of an adjustable inductor and a capacitor. The resonant circuit unit is electrically connected to the titanium-based platinum-plated electrodes. The permanent magnet units are arranged in a rectangular array on the outer wall of the electrolytic cell, and the magnetic field generated by the permanent magnet units is perpendicular to the plane of the titanium-based platinum-plated electrode. The resonant cavity is connected to the outlet of the electrolytic cell, the ultrasonic generator is connected to the bottom of the resonant cavity, and the nanobubble stabilizing layer is composed of silica nanotubes arranged in a rectangular array and is attached to the inner wall of the resonant cavity. The far-infrared radiation plate is made of ceramic material doped with rare earth elements. The far-infrared radiation plate covers the outer surface of the water outlet pipe, which is connected to the water outlet. The tunable microwave generator is installed downstream of the far-infrared radiation plate.

2. The hydrogen-rich ion-active water device according to claim 1, characterized in that, The surface of the titanium-based platinum-plated electrode has a porous structure with a pore size of 5μm-20μm and a porosity of 30%-60%.

3. The hydrogen-rich ion-active water device according to claim 1, characterized in that, The permanent magnet unit is composed of alternating neodymium iron boron magnets and ferrite magnets, and the spacing between adjacent neodymium iron boron magnets and ferrite magnets is 1 / 5 to 1 / 3 of the length of the titanium-based platinum-plated electrode.

4. The hydrogen-rich ion-active water device according to claim 1, characterized in that, The operating frequency of the ultrasonic generator is defined as f. u The operating frequency of the tunable microwave generator is defined as f. m ; Among them, f m =α×f u The f u The value range of α is 28kHz-100kHz, and the value range of α is 1.1-1.

3.

5. The hydrogen-rich ion-active water device according to claim 1, characterized in that, The controller is configured to delay the operation of the ultrasonic generator by a preset time period before driving the tunable microwave generator to start operation.

6. The hydrogen-rich ion-active water device according to claim 1, characterized in that, The controller is configured to increase the operating power of the tunable microwave generator when the operating time of the ultrasonic generator exceeds a preset time.

7. The hydrogen-rich ion-active water device according to claim 6, characterized in that, The controller is configured to increase the operating power of the tunable microwave generator, specifically including: P m =P0×[1+0.05×(T)] u -T0) / T0], where P m P0 represents the increased operating power of the tunable microwave generator, and T represents the reference power of the tunable microwave generator. u T0 is the operating time of the ultrasonic generator, and T0 is the preset time.

8. The hydrogen-rich ion-active water device according to claim 5, characterized in that, The preset time period is 5s-8s.

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