CN106865707B - Production method and device of negative hydrogen ion water - Google Patents
Production method and device of negative hydrogen ion water Download PDFInfo
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- CN106865707B CN106865707B CN201710205393.3A CN201710205393A CN106865707B CN 106865707 B CN106865707 B CN 106865707B CN 201710205393 A CN201710205393 A CN 201710205393A CN 106865707 B CN106865707 B CN 106865707B
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/48—Treatment of water, waste water, or sewage with magnetic or electric fields
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/30—Treatment of water, waste water, or sewage by irradiation
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/68—Treatment of water, waste water, or sewage by addition of specified substances, e.g. trace elements, for ameliorating potable water
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F9/00—Multistage treatment of water, waste water or sewage
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/001—Processes for the treatment of water whereby the filtration technique is of importance
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/28—Treatment of water, waste water, or sewage by sorption
- C02F1/283—Treatment of water, waste water, or sewage by sorption using coal, charred products, or inorganic mixtures containing them
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
Abstract
The invention relates to the field of manufacturing of daily necessities, in particular to a method and a device for producing negative hydrogen ion water. The production method of the negative hydrogen ion water comprises the following steps: mixing 30-60% of zeolite, 20-45% of clay for ceramics, 1-25% of pearl shell, 2-35% of coral calcium and 10-30% of ferric oxide according to the weight ratio, high-temperature oxidizing and firing the mixture to form ceramic balls, and then reducing and firing the ceramic balls at high temperature in a mixed gas containing hydrogen and nitrogen in a volume ratio of 1:92And Fe3O4The ceramic ball of (3), and then a pair of magnets with a magnetic induction of 2T and containing CaH2And Fe3O4The ceramic ball is irradiated in a short distance to make the ceramic ball have magnetic force, and finally the ceramic ball with magnetic force is put into water to form negative hydrogen ions (H)－). The invention relates to a production device of negative hydrogen ion water, which comprises a sediment filter, a carbon block filter, an antibacterial filter, a negative hydrogen ion generator and the like which are sequentially connected from an inlet to an outlet. The method and the device can greatly reduce the production cost of the negative hydrogen ion product.
Description
Technical Field
The invention relates to the field of manufacturing of daily necessities, in particular to a method and a device for producing negative hydrogen ion water.
Background
With the higher pursuit of health, the influence of drinking water quality on human health is gradually emphasized by people.
Negative hydrogen ion (H)－) Also known as hydride ions, until recently has not been included in the field of plasma physics. Hydrogen in this state is negatively charged because it has one more electron on its atom, and becomes a negative ion. The negative hydrogen ions have super-strong oxidation resistance, can effectively remove active oxygen free radicals which bring various skin problems, and convert the active oxygen free radicals into water at the cellular level.
The negative hydrogen ion is the smallest, strongest and most preferable antioxidant substance in the universe discovered at present, and is a very few antioxidant substances discovered so far without any toxic and side effects.
The negative hydrogen ions can improve the capability of an antioxidant system of the organism. It acts on cell mitochondria to enhance the life kinetic energy ATP and improve the metabolic capability of the organism, thereby enhancing the capability of the immune system of the organism.
Not only can resist oxidation, but also can fundamentally enhance the kinetic energy of life, and except for negative hydrogen ions, a second substance which can achieve the effect is not found so far.
The solid negative hydrogen ion product in the prior art needs to be taken by water, so that the consumption of consumers is greatly limited, and the consumers can eat the solid negative hydrogen ion product directly and conveniently without eating the liquid negative hydrogen ion product. The solid negative hydrogen ion product which achieves the same edible effect has high cost compared with the liquid negative hydrogen ion product.
Disclosure of Invention
The invention aims to solve the technical problem of providing a method and a device for producing negative hydrogen ion water, which can produce the negative hydrogen ion water at low cost so as to solve the defects of the prior art.
The specific technical scheme of the invention is as follows:
a process for preparing negative hydrogen ion water includes such steps as proportionally mixing zeolite (30-60 wt.%), clay (20-45 wt.%), pearl shell (1-25 wt.%), calcium coral (2-35 wt.%) and ferric oxide (10-30 wt.%) to form balls, natural drying for 2-3 days, and oxidizing and calcining at 950 deg.C for 8 hr in normal atmosphere to obtain ceramic balls.
Further, the ceramic balls obtained by the oxidation firing are reduced and fired in a mixed gas of hydrogen and nitrogen (hydrogen: nitrogen: 1:9) at 950 ℃ for 12 hours to contain CaH2And Fe3O4The ceramic ball of (1).
Further, a pair of magnets with 2T magnetic induction containing CaH2And Fe3O4The ceramic ball of (2) is irradiated at a short distance for 5 to 10 times with 1 irradiation every 5 seconds. The ceramic balls are provided with magnetic force.
Further, the ceramic ball with magnetic force is put into water, and electric decomposition occurs, so that hydrogen atoms are unimolecular (protium)
). Forming negative hydrogen ions (H)－)。
The invention also discloses a negative hydrogen ion water production device, which comprises a sediment filter, a carbon block filter, an antibacterial filter and a negative hydrogen ion generator which are sequentially connected from an inlet to an outlet.
The sediment filter is of a cylindrical hollow structure, and a perforated shell, an activated carbon layer, a quartz sand layer and a mixed mineral ceramic ball filling layer are sequentially arranged from the side wall to the inside;
the carbon block filter is of a columnar hollow structure, and a perforated shell, a first filtering cotton layer, a carbon block layer, a second filtering cotton layer and a mixed mineral ceramic ball filling layer are sequentially arranged from the side wall to the inside;
the antibacterial filter is of a cylindrical hollow structure, and a perforated shell, an antibacterial granular layer, a filter cotton layer and a mixed mineral ceramic ball filling layer are sequentially arranged from the side wall to the inside;
the negative hydrogen ion generator is of a cylindrical hollow structure, and a perforated shell, a filter cotton layer and a negative hydrogen ion ceramic ball filling layer are sequentially arranged from the side wall to the inside.
Furthermore, the mixed mineral ceramic ball filling layer is formed by extruding a mixture of mixed mineral ceramic balls and activated carbon powder into a transparent barrel layer.
Furthermore, the negative hydrogen ion ceramic ball filling layer is formed by mixing the negative hydrogen ion ceramic balls and the activated carbon powder in the negative hydrogen ion water production method and extruding the mixture into a transparent barrel layer.
Further, the reduction filling layer is filled with the negative potential particles or metal, and the negative potential particle material is any one of metal magnesium, aluminum and zinc or a mixture of metal magnesium, aluminum and zinc in any proportion.
Further, this device of producing takes place can be at the hydrogen-rich water generator of further connection behind the negative hydrogen ion generator, hydrogen-rich water generator is column hollow structure, by the inside foraminiferous shell that sets gradually, first filtration cotton layer, reduction filling layer, second filtration cotton layer, mixed mineral substance ceramic ball filling layer of lateral wall.
The invention has the beneficial effects that:
the invention mainly solves the problem of high cost of the traditional method for preparing the negative hydrogen ion water, and simultaneously solves the problem that the negative hydrogen ion water produced by the traditional method is not rich in mineral substances.
The mixing technology of the hydrogen-rich water and the negative hydrogen ion water adopted in the production device can ensure that the negative hydrogen ions can obtain higher concentration in the mixed solution, and is more favorable for long-time storage of the negative hydrogen ions.
Drawings
Fig. 1 is a schematic view of a silt filter according to the present invention.
Figure 2 is a schematic diagram of the carbon block filter of the present invention.
Fig. 3 is a schematic view of the structure of the antibacterial filter of the present invention.
FIG. 4 is a schematic view of a negative hydrogen ion generator according to the present invention.
Fig. 5 is a schematic structural view of a hydrogen-rich water generator according to the present invention.
Wherein, 1, a sediment filter; 2. a carbon block filter; 3. an antimicrobial filter; 4. a negative hydrogen ion water generator; 5. a hydrogen-rich water generator; 11. a perforated shell of the sediment filter; 12. an activated carbon layer; 13. a quartz sand layer; 14; a mixed mineral ceramic ball filling layer of the sediment filter; 21. a perforated shell of the carbon block filter; 22. a first filter cotton layer of the carbon block filter; 23. a carbon block layer; 24. a second filter cotton layer of the carbon block filter; 25. a mixed mineral ceramic ball filling layer of the carbon block filter; 31. a perforated shell of the antimicrobial filter; 32. an antibacterial granular layer; 33. a filter cotton layer of the antibacterial filter; 34. a mixed mineral ceramic ball filling layer of the antibacterial filter; 41. a perforated shell of the negative hydrogen ion water generator; 42. an active carbon layer of the negative hydrogen ion water generator; 43. a filter cotton layer of the negative hydrogen ion water generator; 44. a negative hydrogen ion ceramic ball filling layer; 51. a perforated shell of the hydrogen-enriched water generator; 52. a first filter cotton layer of the hydrogen-rich water generator; 53. Reducing the filling layer; 54. a second filter cotton layer of the hydrogen-rich water generator; 55. a mixed mineral ceramic ball filling layer of the hydrogen-enriched water generator.
Detailed Description
The production method and the principle of the negative hydrogen ion water are as follows:
(1) mixing 30-60% of zeolite, 20-45% of clay for ceramics, 1-25% of pearl shell, 2-35% of coral calcium and 10-30% of ferric oxide according to a proportion to form a spherical shape, naturally drying for 2-3 days, and oxidizing and sintering for 8 hours at 950 ℃ in normal atmosphere to form the ceramic ball.
Chemical reaction principle of CaCO3＝CaO+CO2↑
(2) The ceramic balls after oxidation sintering are reduced and sintered in mixed gas of hydrogen and nitrogen (hydrogen: nitrogen is 1:9) for 12 hours at 950 ℃ to contain CaH2And Fe3O4The ceramic ball of (1).
CaO +2H of chemical reaction formula principle2＝CaH2+H2O
3Fe2O3+H2＝2Fe3O4+H2O
(3) Using a magnet pair with 2T magnetic induction intensity and containing CaH2And Fe3O4The ceramic ball of (2) is irradiated at a short distance for 5 to 10 times with 1 irradiation every 5 seconds. The ceramic balls are provided with magnetic force.
(4) The ceramic ball with magnetic force is put into water, and electric decomposition occurs, so that hydrogen atoms are monomolecular (protium)
). Forming negative hydrogen ions (H)－). Usually, water (H)2O) can be ionized to "H+And OH－", and" OH－"will bounce back out of the way in a negative field environment. But "H+Can easily enter a negative electric field and is changed into H under the influence of magnetic field energy in an electron-rich state++2e－"producing negative hydrogen ions" H－". Produced "H－"will be transported by the current to the N pole and with a large number of H outside the ceramic ball+"reaction to hydrogen conversion plasma
Hydrogen bubbles were generated from the N pole of the ceramic ball with magnetic force.
Chemical reaction principle of CaH2+2H2O＝Ca(OH)2+2H2↑
The invention also discloses a negative hydrogen ion water production device which has a four-stage or five-stage structure, a first-stage silt filter, a second-stage carbon block filter, a third-stage antibacterial filter, a fourth-stage negative hydrogen ion generator and a fifth-stage hydrogen-rich water (water) generator (the fifth stage can be selected according to actual needs for use or not).
The first stage silt filter is composed of a porous shell and a hollow core layer which is composed of an activated carbon layer, a quartz sand layer and a mixed mineral ceramic ball filling layer.
The first-stage silt filter hollow core layer manufacturing method comprises the following steps: the activated carbon layer is formed by extruding activated carbon powder into a barrel layer and sleeving the barrel layer according to the hierarchical sequence; the quartz sand layer is formed by adding quartz sand particles of 1 mm-3 mm between an active carbon layer of the filter rod and a mixed mineral ceramic ball layer; the mixed mineral ceramic ball filling layer is a transparent barrel layer formed by extruding mixed mineral ceramic balls (multi-functional mineral particles) and activated carbon powder after mixing.
The second-stage carbon block filter is composed of a porous shell and a hollow core layer which is composed of a PP cotton filter core layer, a carbon particle layer, a PP cotton filter core layer and a mixed mineral ceramic ball layer.
The manufacturing method of the second-stage carbon block filter hollow core layer comprises the following steps: the PP cotton filter core layer is a finished product; the carbon particle layer is composed of 1 mm-3 mm of activated carbon particles; the third PP cotton filter core layer is consistent with the first PP cotton filter core layer; the mixed mineral ceramic ball filling layer is a transparent barrel layer formed by extruding mixed mineral ceramic balls (multi-functional mineral particles) and activated carbon powder after mixing.
The third-stage antibacterial filter is composed of a porous shell and a hollow core layer which is composed of an antibacterial particle layer, a PP cotton filter core layer and a mixed mineral ceramic ball filling layer.
The manufacturing method of the third-level antibacterial filter hollow core layer comprises the following steps: the antibacterial particle layer is a transparent barrel layer formed by mixing nano-silver antibacterial ceramic balls and activated carbon powder and extruding the mixture; the PP cotton filter core layer is a finished product; the mixed mineral ceramic ball filling layer is a transparent barrel layer formed by extruding mixed mineral ceramic balls (multi-functional mineral particles) and activated carbon powder after mixing.
The fourth-stage negative hydrogen ion generator is composed of a porous shell and a core layer which is composed of an active carbon layer, a PP cotton filter core layer and a negative hydrogen ion ceramic ball filling layer.
The fourth-stage negative hydrogen ion generator core layer manufacturing method comprises the following steps: the activated carbon layer is a transparent barrel layer formed by mixing activated carbon powder and extruding the mixture; the PP cotton filter core layer is a finished product; the negative hydrogen ion ceramic ball filling layer is a transparent barrel layer formed by extruding a negative hydrogen ion ceramic ball and activated carbon powder after mixing.
The fifth-stage hydrogen-rich water generator is composed of a porous shell and a hollow core layer which is composed of a PP cotton filter core layer, a reduction layer, a PP cotton filter core layer and a mixed mineral ceramic ball filling layer.
The manufacturing method of the hollow core layer of the fifth-stage hydrogen-rich water generator comprises the following steps: the PP cotton filter core layer is a finished product; the reduction layer is formed by extruding a mixture of 100 percent of negative potential balls or metal magnesium strips and activated carbon powder into a transparent barrel layer; the third PP cotton filter core layer is consistent with the first PP cotton filter core layer; the mixed mineral ceramic ball filling layer is a transparent barrel layer formed by mixing and extruding various functional mineral particles and activated carbon powder.
The mixed mineral ceramic ball (multifunctional mineral particles) comprises, by weight, 20% -80% of negative potential ball, 0% -60% of water element ball, 0% -45% of dechlorination ceramic ball, 3% -40% of medical stone ceramic ball, 0% -30% of negative ion ceramic ball, 0% -40% of far infrared ceramic ball, 0% -35% of silver-loaded antibacterial ball, 0% -25% of nano mineral crystal, 0% -30% of descaling molecular ball, 0% -40% of tourmaline ceramic ball and 0% -20% of taste adjusting ball.
Furthermore, the negative potential ball adopts any one of metal magnesium, aluminum and zinc or a mixture of metal magnesium, aluminum and zinc in any proportion, and the granularity is 3 mm-6 mm.
Furthermore, the water element ball comprises, by mass, 20% -70% of metal magnesium powder, 0% -10% of nano-silver antibacterial powder and 10% -50% of kaolin.
Further, the water element ball is prepared according to the following steps: mixing and grinding the components for 8-12h to powder with the particle size less than 50 μm, and roasting at 700-900 ℃ for 2-6h to prepare spheres. The water element ball reduces the negative potential of common water from positive number to 0 mv-negative 500mv, the PH value is 7.3-10.5, and generates a large amount of bubbles to make the water contain hydrogen, and the content of the hydrogen can reach 300-1500 ppb.
Further, the dechlorination ceramic balls comprise 30-90% of food-grade calcium sulfite and 10-70% of clay by mass fraction.
Further, the dechlorination ceramic ball is prepared according to the following steps: mixing 30-90% of food-grade calcium sulfite and 10-70% of clay by mass fraction, and roasting at the temperature of 300-650 ℃ for 0.5-2 h to prepare spheres. The calcium sulfite ball has the advantages of high efficiency, stability, safety, wide application range and the like.
Furthermore, the medical stone ceramic ball comprises, by mass, 0% -50% of natural medical stone, 20% -60% of quartz, 10% -40% of plagioclase feldspar and 10% -50% of kaolin.
Further, the medical stone ceramic ball is prepared according to the following steps: mixing and grinding the components for 6-10h to powder with the particle size less than 50 μm, calcining at the temperature of above 800 ℃ for 2-6h, and preparing into spheres. The medical stone ceramic ball contains various major and trace elements which are beneficial to the growth and development of organisms, rare earth elements and trace amino acid which are called as animal growth regulators, and the elements have various characteristics of good dissolution, mineralization, biological activity, adsorbability, bidirectional regulation on elements in water and pH value of water quality and the like, and are nontoxic and harmless to the organisms.
Furthermore, the negative ion ceramic ball comprises, by mass, 15% -75% of tourmaline, 10% -40% of natural medical stone, 0% -35% of volcanic rock and 20% -50% of clay.
Further, the negative ion ceramic ball is prepared by the following steps: mixing and grinding the components for 6-10h to powder with the particle size less than 50 μm, and roasting at 600-1200 ℃ for 1-2h to prepare spheres. The anion ceramic ball has good effects of filtering water, purifying air, improving human health and the like.
Furthermore, the far infrared ceramic ball comprises, by mass, 10% -50% of iron tourmaline, 5% -40% of crystalline quartz, 0% -30% of titanium oxide, 0% -10% of zirconium oxide, and 20% -70% of kaolin.
Further, the far infrared ceramic ball is prepared by the following steps: mixing and grinding the components for 8-12h to powder with particle size less than 50 μm, calcining at 800 deg.C for 2-6h, and making into spherical shape. Realizing the maximum value of far infrared emissivity. The far infrared ray can warm cells, improve blood circulation, promote metabolism and enhance cell activity. The far infrared ray can effectively destroy hydrogen bonds among water molecules, so that the association degree among the water molecules is reduced, and small molecular group water is generated. And the far infrared ceramic ball can effectively increase the oxygen dissolving capacity and the oxygen dissolving capacity of water, improve the capabilities of water permeation, dissolution, metabolism and the like, and can generate good physiological effect and health care effect on human body as functional drinking water.
Furthermore, the nano-silver antibacterial ball comprises, by mass, 5% -30% of tourmaline, 10% -30% of medical stone, 0% -10% of silver, 15% -40% of zinc oxide, 20% -50% of kaolin and 15% -40% of clay.
Further, the nano-silver antibacterial ball is prepared by the following steps: mixing and grinding the components for 6-10h to powder with the particle size less than 50 μm, calcining at the temperature of above 800 ℃ for 2-6h, and preparing into spheres. The nano-silver antibacterial ball has lasting sterilization and bacteriostasis effects, is harmless to human bodies, has no irritation to skin, and belongs to a safe and non-toxic product. The nano silver antibacterial ball uniformly distributes various metal ions with antibacterial action, such as silver, zinc and the like, into the ceramic ball in a stable form, and solves the problems of color change and high migration speed of the traditional imported silver inorganic antibacterial agent when being added into plastics and fibers. It is inorganic, and has high safety, high heat resistance, high chemical stability, wide spectrum killing and eliminating effect on colibacillus, staphylococcus aureus, candida albicans and other bacteria in over 90%.
Furthermore, the descaling molecular ball comprises 30-70% of tourmaline, 10-40% of titanium oxide, 10-25% of medical stone, 20-50% of kaolin and 0-15% of rare earth material cerium oxide according to mass fraction.
Further, the descaling molecular ball is prepared by the following steps: mixing and grinding the components for 8-12h to powder with particle size less than 50 μm, calcining at 1300 deg.C for 3-8h, and making into spherical shape. The descaling molecular ball has the functions of removing water scale and manufacturing alkaline small molecular group water.
Further, the nano-mineral crystals comprise 30-65% of sepiolite, 10-35% of diatomite, 10-40% of attapulgite and 10-40% of kaolin according to mass fraction.
Further, the nano-mineral crystal is prepared by the following steps: mixing and grinding the components for 6-10h to powder with the particle size less than 50 μm, calcining at the temperature of above 800 ℃ for 2-6h, and preparing into spheres. The adsorption speed of the nano-mineral crystal to harmful gases such as formaldehyde is faster and stronger than that of active carbon. Experiments prove that the strong adsorption effect of the nano-mineral crystals is 10 times of that of the activated carbon, so that the usage amount of the nano-mineral crystals per unit area is far less than that of the activated carbon, and the nano-mineral crystals are formed by compounding pure natural environment mineral materials, have no peculiar smell, are clean and beautiful, have no dust and can be recycled. After being exposed to the sun or heated and baked, the product can be desorbed and regenerated, the service life of the product is far longer than that of the active carbon, and the product is an ideal substitute of the active carbon.
Furthermore, the tourmaline ceramic ball comprises, by mass, 40% -95% of tourmaline, 0% -30% of medical stone and 20% -50% of kaolin.
Further, the tourmaline ceramic ball is prepared by the following steps: mixing and grinding the components for 6-10h to powder with the particle size less than 50 μm, controlling the temperature within 300-800 ℃ for 2-6h, and then preparing the spherical powder. Breaks through the traditional firing process, realizes low-temperature roasting, and keeps the integrity of the internal structure of the tourmaline crystal.
Furthermore, the taste adjusting particles comprise 30-70% of tourmaline, 10-40% of titanium oxide, 5-20% of medical stone, 20-50% of kaolin, 0-10% of potassium chloride and 0-10% of magnesium sulfate by mass.
Further, the mouthfeel adjusting particles are prepared by the following steps: mixing and grinding the components for 6-10h to powder with particle size less than 50 μm, calcining at 1300 deg.C for 3-8h, and making into spherical shape. The taste regulating ball has the functions of regulating taste and producing alkaline small molecular group water.
FIGS. 1 to 5 are diagrams illustrating the construction of each part of the negative hydrogen ion water generating apparatus of the present invention, each stage of the apparatus being a multi-layer columnar hollow structure (the hollow part is not separately shown in the drawings). In actual use, the four-stage structures in fig. 1-4 can be combined together, and the five-stage structures in fig. 1-5 can also be combined together. The specific treatment process comprises the following steps: 1) the water to be treated is pressurized and then sequentially passes through the sediment filter, the carbon block filter, the antibacterial filter and the negative hydrogen ion generator to finally form the negative hydrogen ion water. 2) The water to be treated is pressurized and then sequentially passes through a sediment filter, a carbon block filter, an antibacterial filter, a negative hydrogen ion generator and a hydrogen-rich water (plain water) generator to finally form a mixed liquid of the negative hydrogen ion water and the mineral substance-containing hydrogen-rich water.
The water treatment process of each stage of equipment in the four-stage or five-stage structure is as follows: after water enters from the water inlet of the equipment, the water enters the core from the periphery of the hollow structure under the action of pressure, and then flows from the core to the water storage area at the lower half part of the equipment under the combined action of pressure and gravity, so that the water in the water storage area reaches a certain height and flows out from the water outlet under the action of pressure. The number and the size of the hollow core layers in each stage of equipment can be adjusted and determined according to the production of negative hydrogen ion water with certain concentration or negative hydrogen ion water and mineral-containing hydrogen-rich water (water).
The foregoing is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, various modifications and decorations can be made without departing from the technical principle of the present invention, and these modifications and decorations should also be regarded as the protection scope of the present invention.
Claims (1)
1. The production method of negative hydrogen ion water is characterized by comprising the following steps:
1) mixing 30-60% of zeolite, 20-45% of clay for ceramics, 1-25% of pearl shell, 2-35% of coral calcium and 10-30% of ferric oxide by weight ratio to form a spherical shape, naturally drying for 2-3 days, and oxidizing and sintering at 950 ℃ for 8 hours in normal atmosphere to form ceramic balls;
2) the ceramic ball after oxidation sintering is reacted for 12 hours in mixed gas with the volume ratio of hydrogen to nitrogen being 1:9 at the high temperature of 950 ℃, and then is reduced and sintered to contain CaH2And Fe3O4The ceramic ball of (2);
3) magnet pair containing CaH by utilizing magnetic induction 2T2And Fe3O4The ceramic ball is irradiated in a short distance for 5-10 times at intervals of 5 seconds for 1 time, so that the ceramic ball has magnetic force and negative hydrogen ion ceramic balls are formed;
4) putting the negative hydrogen ion ceramic ball with magnetic force into water to form negative hydrogen ions, and finally preparing negative hydrogen ion water;
the production method of the negative hydrogen ion water is realized by the following production device of the negative hydrogen ion water, which comprises a sediment filter, a carbon block filter, an antibacterial filter and a negative hydrogen ion generator which are sequentially connected from an inlet to an outlet;
the sediment filter is of a cylindrical hollow structure, and a perforated shell, an activated carbon layer, a quartz sand layer and a mixed mineral ceramic ball filling layer are sequentially arranged from the side wall to the inside;
the carbon block filter is of a columnar hollow structure, and a perforated shell, a first filtering cotton layer, a carbon block layer, a second filtering cotton layer and a mixed mineral ceramic ball filling layer are sequentially arranged from the side wall to the inside;
the antibacterial filter is of a cylindrical hollow structure, and a perforated shell, an antibacterial granular layer, a filter cotton layer and a mixed mineral ceramic ball filling layer are sequentially arranged from the side wall to the inside;
the negative hydrogen ion generator is of a columnar hollow structure, and a perforated shell, an activated carbon layer, a filter cotton layer and a negative hydrogen ion ceramic ball filling layer are sequentially arranged from the side wall to the inside;
the mixed mineral ceramic ball filling layer is formed by extruding a mixture of mixed mineral ceramic balls and activated carbon powder into a transparent barrel layer;
the negative hydrogen ion ceramic ball filling layer is formed by extruding the negative hydrogen ion ceramic balls obtained in the step 3) and activated carbon powder into a transparent barrel layer after mixing;
the outlet of the negative hydrogen ion generator is also connected with a hydrogen-rich water generator, the hydrogen-rich water generator is of a cylindrical hollow structure, and a perforated shell, a first filtering cotton layer, a reducing filling layer, a second filtering cotton layer and a mixed mineral ceramic ball filling layer are sequentially arranged from the side wall to the inside;
the reduction filling layer is filled with negative potential particles or metal magnesium strips, wherein the negative potential particles are made of any one of metal magnesium, aluminum and zinc or a mixture of metal magnesium, aluminum and zinc in any proportion.
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| CN112759058A (en) * | 2021-01-13 | 2021-05-07 | 刘建辉 | Electrolytic negative hydrogen ion regenerated water and preparation method thereof |
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