KR102331515B1 - Manufacturing method of hypermineral ionized water, hypermineral ionized water manufactured by the same and cosmetic composition comprising the same - Google Patents

Abstract

The present invention relates to a method for manufacturing hypermineral ionized water, hypermineral ionized water manufactured thereby, and a cosmetic composition including the same. According to the present invention, the method comprises the steps of: collecting seawater consisting of deep coastal bedrock water; manufacturing first seawater by filtering and removing foreign substances or solids precipitated in the collected seawater with a filter, wherein the filter includes filters combining any one or more selected from a group consisting of a sand filter, an activated carbon filter, and a micro filter, and ultrafiltration filter; mixing shungite powder in the first seawater, storing the mixture, and filtering and removing the shungite powder and the precipitated foreign substances or solids with a filter to manufacture second seawater; mixing microporous bodies with the second seawater, performing first heating to evaporate moisture, and separating and collecting only liquid by using a filter to manufacture third seawater; and cooling and crystallizing the third seawater and filtering the crystalized third seawater through a filter to remove solids, thereby manufacturing ionized water. Accordingly, ionized water containing minerals, which are essential for a skin barrier, in high concentrations is manufactured, thereby manufacturing ionized water containing highly concentrated minerals and manufacturing cosmetics showing excellent effects in improving damaged skin by using the same.

Description

Method for producing hypermineral ionized water, hypermineral ionized water prepared thereby, and cosmetic composition comprising the same

The present invention relates to a method for producing hypermineral ionized water, hypermineral ionized water prepared thereby, and a cosmetic composition comprising the same, and more particularly, to a high concentration of minerals by preparing ionized water containing minerals essential for the skin barrier at a high concentration It relates to a method for manufacturing hypermineral ionized water capable of producing ionized water containing .

As the human body's primary barrier, the skin has a function of protecting the organs of the body from external environmental stimuli such as temperature and humidity changes, ultraviolet rays and pollutants.

However, as we age, the secretion of various hormones that control metabolism internally decreases, the function of immune cells and the activity of cells decrease, so that the biosynthesis of immune proteins necessary for the living body and the biosynthesis of the living body proteins is reduced.

In addition, externally, excessive physical and chemical stimulation and stress caused by an increase in free radicals and active harmful oxygen as the amount of ultraviolet rays in the sun's rays increases due to the destruction of the ozone layer externally, and as environmental pollution intensifies, the normal function of the skin is reduced. Reduces skin aging, accelerates skin aging, and damages skin.

In order to prevent skin aging and damage caused by these internal and external factors to maintain healthier and more beautiful skin, the physiologically active substances obtained from various animals, plants, and microorganisms in the past are added to cosmetics and used to maintain the unique function of the skin. Efforts have been made to effectively inhibit skin aging by activating skin cells.

In particular, the biggest indicators of skin aging are an increase in skin wrinkles and a decrease in skin elasticity, and it is known that various factors such as the content of collagen protein and the ability to act on the immune system against the external environment have an effect on this, and the biggest influence What affects the skin moisture content.

Accordingly, various studies for improving skin moisture content are in progress, and attempts have been made to prepare water having physical properties differentiated from existing water in particular.

Among them, Japanese Patent Application Laid-Open No. 6-126287 and Japanese Patent Application Laid-Open No. 8-192172 report a method of changing the structure of water by adding inorganic salts to water. This method uses the principle that the size of is formed small on average, and since this method contains a large amount of inorganic salt, not pure water, there is a limit to its application.

In addition, a method of installing an ultrasonic oscillator in flowing water (Japanese Patent Application Laid-Open No. 6-315682), a method of putting a far-infrared emitting ceramic into stored water (U.S. Patent No. 5,965,007), a method of supersaturating and dissolving oxygen gas at high pressure ( Efforts have been made to change the structure of water without phase transition, such as Japanese Unexamined Patent Publication No. 6-254531), but far-infrared or ultrasonic oscillators do not have a great advantage in reducing the actual interfacial tension or the size of water particles, and also in efficiency. There is a little bit of a problem.

In addition, as a method of filtering impurities in water using a filtration filter, there is a method of activating water by the action of far infrared rays emitted from the ceramic filled in the filter by passing through a filter filled with porous elvan stone and mineral ceramic emitting far infrared rays, but this There is a limit to the application to change the structure of water.

In addition, there is a method of changing the structure of water in the phase transition process (US Patent No. 5,711,950), such as a method of applying a magnetic field during heating and evaporating water and irradiating light of a specific wavelength during the condensation process (U.S. Patent No. 5,711,950), which is a permanent magnet Therefore, there is a disadvantage that the strength of the magnetic field cannot be adjusted, and a wavelength of 640 nm among wavelengths of 610 nm or more is mainly used in the condensation process, but there is a disadvantage that the actual manufacturing efficiency is lowered.

In addition, a method of activating water by a mixing method combining the above methods has been proposed, but the instability of water still exists and thus does not show a great effect.

Domestic Registered Patent No. 10-2233370 (Registered on March 23, 2021) Domestic Registered Patent No. 10-2218534 (Registered on February 16, 2021) Domestic Registered Patent No. 10-0968908 (registered on July 01, 2010)

The present invention can produce ionized water containing highly concentrated minerals by preparing ionized water containing minerals that are essential for the skin barrier at a high concentration, and by using this, hyper that can produce cosmetics showing excellent effects in improving damaged skin It relates to a method for producing mineral ionized water, hypermineral ionized water prepared thereby, and a cosmetic composition comprising the same.

Various problems to be solved by the present invention are not limited to the above-mentioned problems, and other problems not mentioned will be clearly understood by those skilled in the art from the following description.

In the method for producing hypermineral ionized water according to the present invention, the first seawater is prepared by collecting seawater composed of deep coastal bedrock water, and filtering foreign substances or solids deposited in the collected seawater with a filter, but using the filter as the sand Filters that combine any one or more selected from the group consisting of filtration (Sand filter), activated carbon filtration (Activated Carbon filter), micro filtration (Micro filter) and ultra filtration (Ultra filter) are used, 1 After mixing and storing pure git powder in seawater, second seawater is prepared by filtering and removing the pure git powder and the precipitated foreign substances or solids with a filter, and after mixing the microporous body with the second seawater, the first The third seawater is prepared by heating to evaporate moisture, separating and collecting only the liquid using a filter, and cooling and crystallizing the third seawater, and then filtering with a filter to remove solids to prepare ionized water.

In the step of producing ion water by cooling and crystallizing the third seawater and then filtering it with a filter to remove solids, as the filter, any one or more selected from a nano filter or a reverse osmosis filter is combined Filters may be used.

In addition, the present invention includes hypermineral ionized water prepared by the above method.

In addition, the cosmetic composition comprising hypermineral ionized water according to the present invention is hypermineral ionized water, antler collagen, kangaroo claw extract, green tea extract, green lipped mussel oil, polydeoxyribonucleotide sodium (Polydeoxyribonucleotide Sodium), L-carnitine (L -carnitine), ascorbic acid, 1,2-hexanediol (1,2-Hexanediol), purified water, palmitoyl tripeptide-1, hydroxyethylcellulose (Hydroxyethylcellulose), butylene; Butylene Glycol, Polysorbate 20, Sodium Acetylated Hyaluronate, Hydrolyzed Hyaluronic Acid and Glycerin include

The hypermineral ionized water collects seawater composed of deep coastal bedrock water, and filters foreign substances or solids deposited in the collected seawater with a filter to prepare first seawater, but with the filter, sand filter , activated carbon filtration (Activated Carbon filter), micro filtration (Micro filter) and ultra filtration (限外濾過; Ultra filter) is used a combination of any one or more filters are used, the first seawater After mixing and storing the powder, second seawater is prepared by filtering and removing the pure git powder and precipitated foreign substances or solids with a filter, and after mixing the microporous body with the second seawater, the water is evaporated by first heating The third seawater is prepared by separating and collecting only the liquid using a filter, and the third seawater is cooled and crystallized, and then filtered through a filter to remove solids to prepare ionized water.

10 to 20 parts by weight of the hypermineral ionized water, 0.001 to 0.01 parts by weight of antler collagen, 0.2 to 0.6 parts by weight of kangaroo claw extract, 0.08 to 0.12 parts by weight of seaweed extract, 0.08 to 0.12 parts by weight of green lipped mussel oil, polydeoxyribonucleotide Sodium (Polydeoxyribonucleotide Sodium) 0.08 to 0.12 parts by weight, L-carnitine 0.05 to 0.1 parts by weight, Ascorbic acid 0.05 to 0.1 parts by weight, 1,2-hexanediol (1,2-Hexanediol) 1.5 to 2.5 parts by weight, 80 to 120 parts by weight of purified water, 0.01 to 0.1 parts by weight of palmitoyl tripeptide-1, 0.008 to 0.012 parts by weight of hydroxyethylcellulose, butylene glycol (Butylene) Glycol) 0.1 to 0.5 parts by weight, Polysorbate 20 0.008 to 0.012 parts by weight, Sodium Acetylated Hyaluronate 0.001 to 0.005 parts by weight, Hydrolyzed hyaluronic acid (Hydrolyzed Hyaluronic Acid) 0.001 to 0.005 parts by weight and glycerin (Glycerin) may be included in a weight ratio of 0.1 to 1.5 parts by weight.

Specific details of other embodiments are included in the detailed description.

The method for producing hypermineral ionized water according to the present invention can produce ionized water containing highly concentrated minerals by preparing ionized water containing minerals essential for the skin barrier at a high concentration, and by using this, it has an excellent effect in improving damaged skin. Visible cosmetics can be manufactured.

It will be fully understood that embodiments of the technical idea of the present invention may provide various effects not specifically mentioned.

Figure 1a is a photograph showing the skin condition before applying the cosmetic composition according to the embodiment to the face of a subject (42-year-old female), Figure 1b is a cosmetic composition according to the embodiment is applied to the face of the subject (39-year-old female) This is a picture showing the condition of the skin after 4 weeks of use.
Figure 2a is a photograph showing the skin condition before applying the cosmetic composition according to the embodiment to the face of a subject (28 years old female), Figure 2b is a cosmetic composition according to the embodiment is applied to the face of the subject (28 years old female) This is a picture showing the condition of the skin after 4 weeks of use.

Advantages and features of the present invention, and methods for achieving them, will become apparent with reference to the embodiments described below in detail. However, the present invention is not limited to the embodiments described herein and may be embodied in other forms. Rather, the embodiments introduced herein are provided so that the disclosed subject matter may be thorough and complete, and that the spirit of the present invention may be sufficiently conveyed to those skilled in the art.

The terms used in the present application are only used to describe specific embodiments, and are not intended to limit the present invention. The singular expression includes the plural expression unless the context clearly dictates otherwise.

Unless defined otherwise, all terms used herein, including technical or scientific terms, have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Terms such as those defined in a commonly used dictionary should be interpreted as having a meaning consistent with the meaning in the context of the related art, and should not be interpreted in an ideal or excessively formal meaning unless explicitly defined in the present application. does not

Hereinafter, the method for producing hypermineral ionized water according to the present invention will be described in detail with reference to preferred embodiments.

In order to prepare the hypermineral ionized water according to the present invention, first, seawater may be collected.

In the present invention, deep coastal bedrock water may be used as the seawater, and the deep coastal bedrock water generally refers to water eluted from 800 m or more underground within about 1 km from the coast. It refers to the interaction, retention, maturation, and ionization of natural bedrock groundwater and geological time and space conditions that flowed down along the deep subsurface aquifer of the land by intrusion of seawater from the deep ocean through voids or cracks.

The coastal deep bedrock water is affected by the surrounding geology, and thus the useful value as well as the composition of water quality may vary depending on the characteristics of the soil and bedrock underground. Mn), zinc (Zn), iron (Fe), copper (Cu), nickel (Ni), vanadium (V) and selenium (Se) are rich in minerals as well as mineral balance of calcium and magnesium (Mg). has been reported in academia to be similar to human body fluids.

In addition, it contains a lot of inorganic nutrients such as nitrogen (N), phosphorus (P), silicic acid, etc. It also shows efficacy in the removal of active oxygen.

Next, the first seawater can be prepared by filtering and removing foreign substances or solids precipitated in the collected seawater with a filter.

Filtration of foreign substances or solids precipitated in the seawater in the above step may be performed using known filters, for example, the filters include a sand filter, an activated carbon filter, and a microfiltration. (Micro filter) and ultrafiltration (限外濾過; Ultra filter) may be used a combination of any one or more filters selected from the group consisting of.

Next, after mixing and storing the pure git powder in the first seawater, the pure git powder and the precipitated foreign substances or solids are filtered and removed with a filter to produce second seawater.

In the above step, the pure git powder can perform antioxidant, sterilization, stabilization and decomposition functions of pollutants, etc., and is mixed in a weight ratio of 1 to 5 parts by weight of the pure git powder with respect to 100 parts by weight of the total content of the first seawater After that, it can be carried out by maintaining it at a temperature of 20 to 40° C. for 1 to 3 days.

The pure jit powder may be manufactured by pulverizing pure jit minerals, and the shungite _{is a material containing SiO 2} (silicate) and C ₆₀ (fullerene) as main components, and a material containing natural fullerene. means Pure shungite containing more than 90% fullerene is called elite shungite or noble shungite, and pure shungite containing less than 60% fullerene is called normal shungite.

The representative functions of the Sunjit include an antioxidant function, an electromagnetic wave blocking function, a purification and decomposition function of contaminants, and a sterilization and antibacterial function. As a powerful natural antioxidant, Sunjit has the function of increasing human immunity against numerous diseases, purifying water and air by adsorbing pollutants, and has the ability to self-decompose adsorbed pollutants.

In addition, since the Sunjit has antibacterial and sterilizing properties, it has a function of removing more than 99% of only E. coli, Pseudomonas aeruginosa, Staphylococcus aureus and harmful bacteria, and has a function of blocking harmful electromagnetic waves and emitting a large amount of far infrared rays.

The pure jit powder may be used pure jit powder prepared by the following method.

First, the pure jite mineral may be prepared and washed to remove foreign substances attached to the pure jite mineral.

The cleaning of the pure jite mineral may be performed by washing the surface of the pure jite mineral using purified water, thereby removing foreign substances remaining on the surface of the pure jite mineral.

Next, the washed pure jit mineral may be first pulverized to prepare a pulverized pure jit granulated product.

In the above step, by first pulverizing the washed pure jite mineral using a granulator, impurities or organic residues of the pure jite mineral can be removed in a later process, and the first pulverization is performed using a granulator. , may be performed using a known granulator such as a drum granulator or a compression pelletizer, but is not necessarily limited to the granulator described above.

Next, the powdered raw material may be immersed in the mixed solution.

In the above step, impurities or organic residues contained in the coarsely granulated and pulverized pure jite can be removed by immersing the pulverized pure jite in the mixed solution. to 1.0 wt%, persulfate 0.01 to 0.05 wt%, acetic acid 1 to 3 wt%, and the remaining amount of purified water, and may be performed by immersing the milled Sunjit granulated powder in the mixed solution for 20 to 40 minutes.

In addition, as the phosphate compound in the above step, sodium phosphate monobasic (NaH ₂ PO ₄ ), sodium phosphate dibasic (Na ₂ HPO ₄ ), sodium phosphate _tertiary (Na 3 PO ₄ ), potassium phosphate first (KH _{2 )} PO ₄ ), potassium phosphate dibasic (K ₂ HPO ₄ ), ammonium phosphate monobasic ((NH ₄ )H ₂ PO ₄ ), ammonium phosphate dibasic ((NH ₄ ) ₂ HPO ₄ ), and ammonium tertiary phosphate (( Any one or more selected from the group consisting of NH ₄ ) ₃ PO ₄ ) may be used, and as the persulfate, ammonium persulfate ((NH ₄ ) ₂ S ₂ O ₈ ), sodium persulfate (Na ₂ S ₂ O _{8 )} ) or potassium persulfate (K ₂ O ₈ S ₂ ) Any one or more selected from may be used.

Then, after separating the granulated and pulverized raw material from the mixed solution, the granulated and pulverized raw material may be heated and calcined using a kiln.

In the above step, it is possible to remove and activate the contaminants adsorbed on the micropores of the granulated pure Jit by heating the separated pure Jit granulated and pulverized product using a kiln. After being put into the kiln, it can be carried out by heating at a temperature of 1,100 to 1,300 ℃ for 50 to 100 minutes.

Next, a second pulverization of the calcined pulverized pure jit may be performed to prepare a pulverized pulverized pure jite.

In the above step, it may be carried out by pulverizing the calcined pure jit granulated product using a ball mill or various known pulverizers. can do.

Next, impurities may be removed from the pulverized material of pure Jit and sterilized to prepare a pure Jit powder.

In the above step, impurities such as heavy metals that may remain in the pulverized pure jit can be removed by rotating the pulverized pure jit in a rotary tub equipped with a magnet. It is possible to remove impurities such as heavy metals that may be included in the Sunjit fine pulverized product by rotating it for 10 to 20 minutes at a rotation speed of 500 to 1000 RPM after being put into the installed rotary tube.

Subsequently, the third seawater can be prepared by mixing the microporous body with the second seawater, evaporating moisture by first heating, and separating and collecting only the liquid using a filter.

In the above step, by mixing the microporous body with the second seawater and heating it, moisture and harmful components with a low vaporization point contained in the second seawater can be removed, and the microporous body is the second seawater is rapidly heated It can be prevented and harmful components can be easily collected on the surface of the microporous body.

In the above step, the second seawater is mixed in a weight ratio of 1 to 5 parts by weight with respect to 100 parts by weight of the total content of seawater, and then heated at a temperature of 80 to 85° C. for 5 to 10 hours to evaporate moisture, thereby concentrating the mineral component. It is possible to produce a third seawater with

As the microporous body, a microporous body prepared by the following method may be used.

First, to prepare the microporous body, unburned carbon powder, fly ash, loess and dredged soil are prepared, and water can be prepared as a binder for molding the unburned carbon powder, fly ash, loess and dredged soil into a certain shape. At this time, the loess and dredged soil may be used to improve the caking properties of unburned carbon powder and fly ash.

In addition, the unburned carbon powder, fly ash, loess and dredged soil are each mixed in a weight ratio of 10 to 15 parts by weight of unburned carbon powder, 8 to 12 parts by weight of fly ash, 2 to 4 parts by weight of loess and 3 to 7 parts by weight of dredged soil, Water may be mixed in a weight ratio of 30 to 40 parts by weight based on 100 parts by weight of the total unburned carbon powder, fly ash, loess and dredged soil.

Next, after preparing a mixture by mixing the unburned carbon powder, fly ash, loess, dredged earth and water, the mixture may be molded into a predetermined shape to form a molded body.

That is, the molded body is mixed in a weight ratio of 10 to 15 parts by weight of unburned carbon powder, 8 to 12 parts by weight of fly ash, 2 to 4 parts by weight of loess and 3 to 7 parts by weight of dredged soil, and the unburned carbon powder, fly ash, loess and dredged soil. After preparing a mixture by mixing in a weight ratio of 30 to 40 parts by weight of water with respect to 100 parts by weight of the total, a molded body can be manufactured by molding the mixture into various shapes such as spherical shape and pellet shape.

Next, the molded body may be heated and fired.

The firing of the molded body may be fired by heating the molded body in a kiln, for example, a tunnel kiln or a discontinuous kiln may be used as the kiln, and the kiln has an internal temperature of 400 to 450° C. It can be maintained at a temperature of, and then fired in an oxidizing or reducing (neutral) atmosphere for 3 to 5 hours while gradually raising the temperature to 1200 to 1300 °C after putting the molded body inside the kiln.

Then, the calcined molded body may be cooled to prepare a microporous body.

Cooling of the fired molded body in the above step can be cooled for 1 to 3 hours at a temperature of 200 to 250 ℃ after taking out the molded body from the kiln, and then cooled at a temperature of 30 to 50 ℃ for 10 to 12 hours, By cooling the fired molded body through the two-step cooling process as described above, it is possible to prevent surface cracking and a decrease in compressive strength of the fired molded body due to rapid cooling, and also, shrinkage can be prevented.

Next, after cooling and crystallizing the third seawater, it is filtered through a filter to remove solids, thereby producing hypermineral ionized water in which minerals are concentrated at a high concentration.

In the above step, after the third seawater is introduced into the cooling device, the temperature of the cooling device is lowered to lower the temperature of the third seawater to form a crystallized solid, and the crystallized solid is filtered and removed with a filter. Hypermineral ionized water can be prepared.

That is, in the above step, as the temperature of the cooling device is lowered, solids containing salt contained in the third seawater accommodated in the cooling device may be precipitated. By maintaining and cooling for 10 to 30 hours, it is possible to prepare hypermineral ionized water in which minerals are concentrated at a high concentration.

In addition, the filtration of the crystallized solid in the above step may be performed using known filters, for example, as the filters, any one or more selected from nanofiltration or reverse osmosis filter Combination filters can be used, and the membrane module form of the nano filter and the reverse osmosis filter is a tubular, a hollow fiber, It does not matter whether any shape such as a spiral wound or a plate and frame may be used, and the material of the membrane is not particularly limited.

According to the present invention, hypermineral ionized water can be prepared through the process as described above. As a result of measuring the physical properties of the hypermineral ionized water at a temperature of (20±5)°C and a humidity (36±5)% RH, the following [Table 1] ], it can be seen that minerals are abundantly included.

Hereinafter, a cosmetic composition containing hypermineral ionized water according to the present invention will be described in detail with reference to preferred examples.

The cosmetic composition comprising hypermineral ionized water according to the present invention is hypermineral ionized water, antler collagen, kangaroo claw extract, green tea extract, green lipped mussel oil, polydeoxyribonucleotide sodium (Polydeoxyribonucleotide Sodium), L-carnitine (L-carnitine) ), ascorbic acid, 1,2-hexanediol, purified water, palmitoyl tripeptide-1, hydroxyethylcellulose, butylene glycol (Butylene Glycol), polysorbate 20 (Polysorbate 20), sodium acetylated hyaluronate (Sodium Acetylated Hyaluronate), hydrolyzed hyaluronic acid (Hydrolyzed Hyaluronic Acid) and glycerin (Glycerin). .

In addition, the cosmetic comprising the cosmetic pigment according to the present invention contains 10 to 20 parts by weight of hypermineral ionized water, 0.001 to 0.01 parts by weight of antler collagen, 0.2 to 0.6 parts by weight of kangaroo claw extract, 0.08 to 0.12 parts by weight of green tea extract, green lip Mussel oil 0.08 to 0.12 parts by weight, Polydeoxyribonucleotide Sodium 0.08 to 0.12 parts by weight, L-carnitine 0.05 to 0.1 parts by weight, Ascorbic acid 0.05 to 0.1 parts by weight, 1.5 to 2.5 parts by weight of 1,2-hexanediol (1,2-Hexanediol), 80 to 120 parts by weight of purified water, 0.01 to 0.1 parts by weight of Palmitoyl Tripeptide-1, Hydroxyethylcellulose ) 0.008 to 0.012 parts by weight, Butylene Glycol 0.1 to 0.5 parts by weight, Polysorbate 20 0.008 to 0.012 parts by weight, Sodium Acetylated Hyaluronate 0.001 to 0.005 parts by weight, hydrolyzed hyaluronic acid (Hydrolyzed Hyaluronic Acid) 0.001 to 0.005 parts by weight and glycerin (Glycerin) may be included in a weight ratio of 0.1 to 1.5 parts by weight.

The hypermineral ionized water may be prepared from deep coastal bedrock water, and the deep coastal bedrock water generally refers to water eluted from 800 m or more underground within about 1 km from the coast. It refers to the interaction, retention, maturation, and ionization of natural bedrock groundwater and geological time and space conditions that flow down through the cracks in the deep ocean seawater and the deep underground aquifer on land.

The coastal deep bedrock water is affected by the surrounding geology, and thus the useful value as well as the composition of water quality may vary depending on the characteristics of the soil and bedrock underground. Mn), zinc (Zn), iron (Fe), copper (Cu), nickel (Ni), vanadium (V) and selenium (Se) are rich in minerals as well as mineral balance of calcium and magnesium (Mg). has been reported in academia to be similar to human body fluids.

In addition, it contains a lot of inorganic nutrients such as nitrogen (N), phosphorus (P), silicic acid, etc. It also shows efficacy in the removal of active oxygen.

The antler collagen may be prepared from antlers, which are keratinized antlers of various deer such as hemp or plum belonging to the deer family. Ankak is salty in taste, warm in nature, and non-toxic. It enters the liver and kidneys. Ankak promotes blood circulation, eliminates blood stasis, helps kidney and liver functions, and contains a large amount of calcium to make bones strong.

In these antlers, sialic acid, hexose, pentose, hexosamine and uronic acid, free amino acids and minerals, and special fatty acids widely distributed in animal tissues, It has been reported that prostaglandins and gangliosides, a type of glycolipids, exist.

As the nocturnal collagen, the nocturnal collagen prepared by the following method may be used.

First, after preparing the antlers, it can be washed and cut into regular length units.

In the above step, the antler refers to ossified antlers of a deer. For example, the antler is prepared by preparing one or more antlers selected from the group consisting of red deer, Japanese deer, wapiti deer, and reindeer. can be cut to a length of 10 to 15 cm.

Next, it is possible to prepare a hot water extract from the green leaf from which the useful components of the green leaf are extracted by mixing the chopped green leaf with purified water and heating it.

In the above step, after mixing in a weight ratio of 5,000 to 10,000 parts by weight of purified water to 100 parts by weight of the whole minced antler, heated at a temperature of 80 to 90° C. for 20 to 40 hours to prepare a hot water extract from which useful components of antlers are extracted can do.

Next, the antler hot water extract can be filtered to remove solids, and then concentrated to prepare an antler horn concentrate.

In the above step, the antler horn hot water extract is filtered with a known filter to prepare a antler filtrate, and the antler horn filtrate is heated at a temperature of 75 to 85° C. to remove moisture, thereby preparing a gel-type green kelp concentrate.

Subsequently, the antler concentrate is mixed with the first enzyme to perform primary enzymatic decomposition, and then heated to inactivate the first enzyme, and the first enzymatically decomposed antler concentrate may be cooled.

In the above step, as the first enzyme, a commercially available proteolytic enzyme may be used. For example, as the first enzyme, the endoprotease Alcalase, Nutraase, Protamex, and Novo. Any one or more proteolytic enzymes selected from the group consisting of pro and formea may be used.

In addition, in the above step, after mixing the antler concentrate with the first enzyme, it is first enzymatically decomposed at a temperature of 45 to 55 ° C. The first enzyme is inactivated by heating, and the cooling may be performed by storing the first enzymatically decomposed heated antler concentrate at a temperature of 25 to 45°C.

Next, the first decomposed antler concentrate is mixed with a second enzyme for secondary enzymatic decomposition, and then heated to inactivate the second enzyme, and the second enzymatically decomposed antler concentrate may be cooled.

In the above step, as the second enzyme, a commercially available proteolytic enzyme may be used. For example, as the second enzyme, any one selected from exopeptidase flavourzyme or protana More than one proteolytic enzyme may be used.

In addition, in the above step, after mixing the first decomposed antler concentrate with a second enzyme, it is subjected to secondary enzymatic decomposition at a temperature of 45 to 55 ° C. The second enzyme is inactivated by heating to 35 minutes, and the cooling may be performed by storing the second enzymatically decomposed heated antler concentrate at a temperature of 25 to 45°C.

Next, by drying the second enzymatically decomposed antler horn concentrate, it is possible to prepare antler collagen.

In the above step, by drying the secondary enzymatically decomposed antler horn concentrate to remove moisture, it is possible to prepare a gel-state low molecular weight antler horn collagen.

The kangaroo claw extract kangaroo claw (not glass monohydrate flaviviruses Douce (Anigozanthos flavidus)) a may be prepared by extracting the kangaroo claw (not glass monohydrate flaviviruses Douce (Anigozanthos flavidus)) is a perennial plant of monocotyledonous plants , is native to Western Australia, and is distributed in South Africa, Australia, New Guinea, and tropical South America, and inhabits dry sand, gravel fields, wetlands, and around drainage channels.

In the kangaroo claw, the rhizome extends sideways, the diameter reaches 50 cm, there is no main stem, and up to 10 flower stems come up together with the leaves, the length is about 1-1.5 m, and the flower branches are split at the upper part. Flower stalks grow to about 0.5-1.5 m in height.

The kangaroo claw extract can control both the stability of collagen and elastin, organize collagen fibers in the extracellular matrix (ECM) to enhance the stiffness or elasticity of almost all cells in the body, and reconstruct the structure of the skin over time. It is known that it can help reduce wrinkles on the eyes and neck as well as sagging skin.

The kangaroo claw extract may be prepared by extracting any one or more selected from flowers, leaves, or stems of kangaroo claws, and preferably, a kangaroo claw flower extract prepared by extracting flowers of kangaroo claws may be used, for example, , The kangaroo claw flower extract may be a kangaroo claw flower extract prepared by the following method.

In order to prepare the kangaroo claw flower extract, first, the kangaroo claw flower may be prepared and then washed.

Next, the washed kangaroo claw flowers may be pulverized to a certain particle size.

In the above step, the active ingredient of the kangaroo claw flower can be effectively extracted by pulverizing the washed kangaroo claw flower to a certain particle size. It can be crushed to become

When the particle diameter of the washed kangaroo claw flower is pulverized to less than 100 μm in the above step, it takes a long time to pulverize, and the particles are too small to cause agglomeration between the particles in a later process, and the particle diameter exceeds 3000 μm When it is pulverized, it may be difficult to effectively extract useful ingredients from the kangaroo claw flower in a short time.

Then, the pulverized kangaroo claw flower may be extracted to prepare a kangaroo claw flower extract.

Extraction of the pulverized kangaroo claw flower in the above step may be performed using a variety of known extraction methods such as hot water extraction, organic solvent extraction, ultrasonic extraction, and supercritical extraction.

For example, the ultrasonic extraction method is an extraction solvent for the sample, which is water, C1-C6 anhydrous or hydrous lower alcohol, acetone, butylene glycol, ethyl acetate, diethyl acetate, diethyl ether, benzene, chloroform and a group consisting of hexane After adding any one or more extraction solvents selected from 10 to 20 times by volume, it may mean an extraction method performed using an ultrasonic extraction method for 1 hour to 10 hours, preferably 1 hour to 4 hours.

In addition, the supercritical extraction method is a supercritical fluid extraction reactor (Natex, Autstria) in 500-700 mL of ethanol (99.5%) as an auxiliary solvent with the pulverized kangaroo claw flower, the temperature in the reactor is 65 ℃, the pressure is 450 bar, S/F ratio (supercritical fluid kg/Feed kg) may refer to a method of extraction under the condition of 35.

The green tea extract is prepared using green tea, and the green tea extract prepared by the following method may be used.

In order to prepare the green tea extract, first, green tea can be prepared and then washed.

The green tea ( Salicornia spp. ) is a representative edible and medicinal halophyte that grows wild in Korea as an annual grass of the family Myopodaceae. The green tea has been used as a folk medicine for a long time for vision loss, indigestion, gastrointestinal disease, hepatitis, kidney disease, etc., and has been scientifically proven to have antioxidant, anti-diabetic, anti-cancer, anti-hypertensive, anti-hyperlipidemia, and skin whitening effects.

Next, the washed green tea can be immersed in the mixed solution.

In the above step, by immersing the washed green tea in a mixed solution, it is possible to prevent discoloration or easy deterioration of green tea, and the mixed solution may consist of grape juice, lemon juice and bamboo salt water.

In addition, in the above step, the grape juice is good for preventing blood clots and preventing adult diseases such as high blood pressure, arteriosclerosis and heart disease, and helps to improve memory. It is effective in preventing colds, headaches, etc., and the bamboo salt water sterilizes the green tea to prevent easy spoilage.

In addition, the lemon juice and bamboo salt water can prevent the green tea from discoloring over time, and the mixed solution is prepared by mixing 1 part by weight of grape juice, 1 part by weight of lemon juice, and 8 parts by weight of bamboo salt solution, The bamboo salt water may have a concentration of 1 to 3% by weight.

In addition, in the above step, the washed green tea can be immersed in a mixed solution and maintained at a temperature of 20 to 25° C. for 50 to 100 minutes.

Next, after taking out the green tea immersed in the mixed solution, the green tea can be steamed with steam.

In the above step, the green tea impregnated with the components of grape juice, lemon juice and bamboo salt water is mixed with a mixture of cinnamon powder and sugar, and then steamed in a steamer. In the above step, the cinnamon powder and sugar are cinnamon powder 20 to 30 parts by weight and 10 to 20 parts by weight of sugar are mixed, and heated in a steamer with steam at 120 to 140° C. for 20 to 40 minutes and steamed.

In the above step, the cinnamon powder enhances immunity and promotes blood circulation to help prevent vascular diseases, and has food poisoning prevention, sterilization and insecticidal effects, and the sugar enhances the surface gloss and sugar content of immersed green tea, and has an antiseptic effect. Storage can be improved.

Then, it may be dried after grinding the steamed green tea.

In the above step, the drying efficiency of the green tea can be improved by grinding the steamed green tea to a large particle state and then drying. For example, after pulverizing the green tea to a size of 0.5 to 2 mm, the pulverized green tea may be carried out by drying at 25 to 35° C. for 20 to 30 hours.

Next, by extracting the dried green tea, it is possible to prepare a green tea extract.

Extraction of the dried green tea in the above step may be performed using a variety of known extraction methods such as hot water extraction, organic solvent extraction, ultrasonic extraction, supercritical extraction, and the like.

The green-lipped mussel oil is manufactured using green-lipped mussels (Perna Canaliculus), which is a kind of mussels that inhabit the coast of New Zealand and is called green-lipped mussel, and its scientific name is Perna. Canaliculus.

It has been reported that the green-lipped mussel contains omega unsaturated fatty acids related to antioxidant and anti-inflammatory properties, that is, a unique component that cannot be seen in mussels that are native to other regions, because the green-lipped mussel feeds mainly on plankton that has evolved to resist intense ultraviolet rays.

In addition, the unsaturated fatty acids found in the green lipped mussel have been known through clinical trials to have a 200-fold stronger anti-inflammatory effect than fish oil, linseed oil, evening primrose oil, and the like containing omega-3 fatty acids. Omega-3 fatty acids have been found to inhibit the occurrence of inflammatory diseases such as atherosclerosis and rheumatoid arthritis by interfering with the production of inflammatory mediators made from omega-6 fatty acids by competing with omega-6 linoleic acid. there is a bar

In the present invention, green-lipped mussel oil prepared by the following method may be used as the green-lipped mussel oil.

First, the skin of the green-lipped mussel may be removed, and the green-lipped mussel from which the skin has been removed may be washed.

In the above step, the green-lipped mussel from which the skin has been removed can be washed with a sodium bicarbonate solution having a temperature of 10 to 20° C. and a concentration range of 1 to 3 (w/w)%, and the sodium bicarbonate (NaHCO3) is a food product. It is also used as an additive, is non-toxic, and may have functions such as penetration, diffusion, and expansion.

Next, the washed green-lipped mussels may be dried.

Drying of the washed green-lipped mussel may consist of a first drying and a second drying, wherein the first drying is performed by drying the washed green-lipped mussel at a temperature of 70 to 80° C. for 3 to 5 hours. Residual moisture in green-lipped mussels can be removed primarily.

In addition, in the second drying, the first dried green-lipped mussel may be dried with hot air, and the second drying is performed by applying hot air to the first dried green-lipped mussel at a temperature of 110 to 130° C. for 1 to 3 hours. This can be done by adding

Next, the second dried green-lipped mussel can be pulverized and then aged to prepare an aged green-lipped mussel powder.

In the above step, the grinding of the second dried green-lipped mussel is pulverized by pulverizing the second dried green-lipped mussel to a particle size of 5 to 10 mm, and the aging of the powdered green-lipped mussel is the powdered green mussel. It can be carried out by storing the lipped mussels at a temperature of 5 to 10° C. for 3 to 7 hours.

Then, the green-lipped mussel aged powder can be enzymatically decomposed by mixing the enzyme and acid and storing the mixture.

That is, in the above step, the enzyme and acid are mixed in the aged powder of green lipped mussel, and then the aged powder of green lipped mussel in which the enzyme and acid are mixed is stored at a temperature of 36 to 38° C. for 20 to 30 hours, thereby enzymatic decomposition. .

In the above step, known commercially available protease (Protease), chitinase (chitinase), pectinase (Pectinase) and xylanase (Xylanase) are used as the enzyme as the enzyme, and citric acid and ascortic acid are used as the acid. Binic acid may be used, specifically, 0.01 to 0.03 parts by weight of the protease, 0.03 to 0.05 parts by weight of chitinase, and pectinase, based on 100 parts by weight of the whole aged powder of green lipped mussel. 0.005 to 0.009 parts by weight, 0.008 to 0.012 parts by weight of Xylanase, 0.01 to 0.1 parts by weight of citric acid, and 0.01 to 0.1 parts by weight of ascorbic acid may be mixed in a weight ratio.

Next, the fermented green-lipped mussel can be prepared by mixing the lactic acid bacteria culture solution with the enzyme-decomposed green-lipped mussel aged powder and fermenting it.

In the above step, after mixing in a weight ratio of 1 to 3 parts by weight of the lactic acid bacteria culture solution to 100 parts by weight of the enzymatically decomposed green-lipped mussel aged powder, fermentation may be performed at a temperature of 40 to 42° C. for 20 to 30 hours.

In addition, in the above step, the lactic acid bacteria culture medium was adjusted to pH 2.8 to 3.2 using 1.2N HCl, and then the lactic acid strain was separated from kimchi, and the separated lactic acid strain was used in MRS broth (Oxoid, England). After incubation for 20 to 25 hours at 37~39℃, ^{diluted to 1×1.0 8} to 5×1.0 ⁸ CFU/mL, and then centrifuged at 10,000 to 15,000 rpm for 10 to 15 minutes to separate only the supernatant And, after filtering the supernatant (Supernatant) with a 0.45㎛ syringe filter (syringe filter), diluted by mixing in a weight ratio of 1,000 to 2,000 parts by weight of sterilized distilled water with respect to 100 parts by weight of the filtered supernatant, the lactic acid bacteria is As a lactic acid strain isolated from fermented food, kimchi, specifically, the lactic acid strain includes Lactobacillus curvatus , Weissella viridescens , Lactobacillus plantarum ) and Any one or more known lactic acid strains selected from the group consisting of Leuconostoc lactis may be used.

Next, the green-lipped mussel oil can be prepared by separating the oil using the fermented green-lipped mussel.

The configuration, such as separating the oil using the green-lipped mussel fermented product in the above step, is a known technique to those of ordinary skill in the art, and for convenience of explanation and clarity of the technical idea of the present invention, A detailed description thereof will be omitted.

The polydeoxyribonucleotide sodium (Polydeoxyribonucleotide Sodium) can relieve inflammation of damaged tissues and promote cell regeneration. For example, the polydeoxyribonucleotide sodium (Polydeoxyribonucleotide Sodium) interacts with adenosine receptors to induce blood vessels By promoting the expression of endothelial growth factor, it can promote wound healing, promote epithelial cell growth, promote extracellular matrix maturation, and promote angiogenesis by increasing the density of microvessels.

The L-carnitine binds to fatty acids and transports them as energy, and fatty acids suppress feedback, secrete ATP to increase lipolytic enzyme activity, and can cause hydrolysis of triglycerides.

Ascorbic acid is involved in the synthesis of collagen, which is a major protein constituting connective tissues such as skin, skeleton, blood vessels, and cartilage, and is used as a coenzyme for various enzymatic reactions in vivo. In addition, the ascorbic acid (Ascorbic acid) has the effect of increasing the absorption of vegetable iron not bound to hemoglobin by converting iron in the small intestine to a reduced form and preventing inflammation or aging.

The 1,2-hexanediol (1,2-Hexanediol) may be used as a solvent, and the solvent is used to increase moisture feeling and moisturizing power, and to effectively dissolve various compositions included in cosmetics. can be used

The purified water (Water) and palmitoyl tripeptide-1 (Palmitoyl Tripeptide-1) may be used as a humectant (Humectant), the humectant (Humectant) may be included to absorb or preserve moisture to enhance moisturizing power.

The hydroxyethylcellulose (Hydroxyethylcellulose) may be used as a thickener (Viscosity Increasing Agent), the thickener (Viscosity Increasing Agent) may be included to increase the viscosity of the cosmetic or to adjust the viscosity.

The Butylene Glycol, Polysorbate 20, Sodium Acetylated Hyaluronate and Hydrolyzed Hyaluronic Acid are skin conditioning It can be used as an agent (Skin-Conditioning Agent), wherein the skin-conditioning agent (Skin-Conditioning Agent) improves the functional and cosmetic effects of cosmetics, and may be included to enhance the effects of nutrition, soothing and trouble improvement, whitening, etc. .

The glycerin may be used as a pH adjuster, and the pH adjuster may be included to adjust the final pH of the cosmetic within the range stipulated in the cosmetics law.

Hereinafter, examples and comparative examples of the cosmetic composition containing hypermineral ionized water according to the present invention will be described in more detail.

<Example>

Hypermineral ionized water 15 parts by weight, antler collagen 0.008 parts by weight, kangaroo claw extract 0.4 parts by weight, seaweed extract 0.1 parts by weight, green lipped mussel oil 0.1 parts by weight, Polydeoxyribonucleotide Sodium 0.1 parts by weight, L- Carnitine (L-carnitine) 0.07 parts by weight, ascorbic acid (Ascorbic acid) 0.08 parts by weight, 1,2-hexanediol (1,2-Hexanediol) 2 parts by weight, purified water 100 parts by weight, palmitoyl tripeptide-1 (Palmitoyl) Tripeptide-1) 0.07 parts by weight, Hydroxyethylcellulose 0.01 parts by weight, Butylene Glycol 0.3 parts by weight, Polysorbate 20 0.01 parts by weight, Sodium acetylated hyaluronate A cosmetic composition was prepared by mixing 0.003 parts by weight of sodium acetate, 0.003 parts by weight of hydrolyzed hyaluronic acid, and 0.8 parts by weight of glycerin.

< Comparative Example >

A cosmetic composition was prepared using the same composition as in Example, but in Comparative Example, a cosmetic composition was prepared without including hypermineral ionized water, unlike in Example.

1. Measurement of moisture content

For the cosmetic compositions according to Examples and Comparative Examples, the skin moisturizing effect was measured using Corneometer CM 825 (Courage Khazaka Electronic GmbH, Germany). Measurement was carried out in the following manner.

For each sample, 30 women in their 20s and 30s were divided into 3 groups of 10 people per group, and the Examples and Comparative Examples were applied to the face twice daily for 1 month. Before application start, the value measured using Corneometer CM 825 in a constant temperature and humidity room with a temperature of 25±1℃ and a relative humidity of 43±3% is the default value, and the same conditions after 1 week, 2 weeks, 3 weeks, and 4 weeks have elapsed. to evaluate the increase rate.

The measured value was used as an average of the values obtained by measuring three times, and the increase rate using the average value of 30 subjects is shown in [Table 2].

division 1 week later 2 weeks later after 3 weeks after 4 weeks Example 31.3 36.5 38.8 42.7 comparative example 20.6 22.8 26.4 29.7

Referring to [Table 2], it was confirmed that the effect of increasing the skin moisture content of the cosmetic composition according to the Example was superior to that of the cosmetic composition according to the Comparative Example. Able to know.

2. Measurement of trans-epidermal water loss (TEWL)

The amount of transdermal water loss (TEWL) was evaluated using Tewameter TM 210 (C+K electronic GmbH, Germany) for the cosmetic compositions according to the Examples and Comparative Examples. A specific evaluation method is as follows.

For each sample, 30 women in their 20s and 30s were divided into 3 groups of 10 people per group, and 3 groups of Examples and Comparative Examples were applied to the entire face, centering around the eyes.

After 2 hours, 4 hours, 6 hours, and 8 hours after application, the amount of transdermal water loss was measured using Tewameter TM 210. The measured values were used by averaging the values obtained by measuring three times, and the measured values using the average value of 30 subjects are shown in [Table 3].

division after 2 hours after 4 hours after 6 hours after 8 hours Example 14.8 11.2 8.5 6.1 comparative example 18.2 15.7 13.7 12.3

Referring to [Table 3], it was confirmed that the amount of transdermal moisture loss of the cosmetic composition according to the Example was smaller than that of the cosmetic composition according to the Comparative Example, and therefore, it can be seen that the cosmetic composition according to the Example has excellent skin moisturizing power. have.

3. Skin irritation test of cosmetic composition

Stimulation clinical trials for the cosmetic composition according to the examples were carried out as follows.

First, the clinical trial was conducted on 30 healthy subjects (10 men and 20 women) between the ages of 10 and 50. It was confirmed that no other products such as steroids or antibiotics were used from 2 weeks before the start of the experiment until the end of the experiment. .

^{And to all test subjects, apply a certain amount (2mg/cm 2} ) of the cosmetic composition according to the embodiment to the skin area without any problems after washing with soap, and observe the skin condition (erythema, edema, papule, etc.) 24 hours after [ Qualitative evaluation was performed through the evaluation table shown in Table 4].

experimental item subjective score

degree of stimulation a: The skin becomes very red and the itchiness is strong. b: The skin is slightly red and there is itching. c: The skin becomes slightly red and there is irritation. d: There is no change in skin condition, but there is slight irritation e: No irritation or change in skin condition

The evaluation results of the test subjects for the degree of stimulation in [Table 4] are shown in [Table 5] below.

experimental item subjective score Evaluation results

degree of stimulation a: The skin becomes very red and the itching is strong. - b: The skin is slightly red and there is itching. - c: The skin becomes slightly red and there is irritation. - d: There is no change in skin condition, but there is slight irritation 2 e: No irritation or change in skin condition 28

As can be seen from [Table 5] above, it was confirmed that the cosmetic composition according to the example was a safe material with little irritation such as erythema.

4. Degree of formulation stabilization

The formulation stabilization degree of the cosmetic compositions according to the above Examples and Comparative Examples was evaluated.

The evaluation of the formulation stabilization degree was carried out by checking the phase stability by storing the cosmetic compositions prepared according to Examples and Comparative Examples at a temperature of 40°C, room temperature, and -20°C for 40 days, respectively, and the results are shown in the following [[] Table 6].

division Example comparative example 40℃ Good Good room temperature Good Good -20℃ Good Good

Referring to [Table 6], it was confirmed that formulation stability was ensured in the case of the cosmetic compositions according to Examples and Comparative Examples.

5. Skin improvement evaluation

The cosmetic composition according to the example was applied to the subject's face twice a day in the morning and evening, and a certain amount (3g) was applied, and after 4 weeks had elapsed, the subject's skin improvement was visually evaluated.

Figure 1a is a photograph showing the skin condition before applying the cosmetic composition according to the embodiment to the face of a subject (42-year-old female), Figure 1b is a cosmetic composition according to the embodiment is applied to the face of the subject (39-year-old female) This is a picture showing the condition of the skin after 4 weeks of use.

In addition, Figure 2a is a photograph showing the skin condition before applying the cosmetic composition according to the embodiment to the face of a subject (28 years old female), Figure 2b is a cosmetic composition according to the embodiment to the face of the subject (28 years old female) This is a picture showing the condition of the skin after 4 weeks of application and use.

1A to 2B, the skin condition (FIGS. 1B and 2B) after 4 weeks have elapsed after applying the cosmetic composition according to the embodiment to the face of a subject (39-year-old female) and using it before use (FIG. 1A) and FIG. 2a).

As described above, a preferred embodiment of the present invention has been described, but those of ordinary skill in the art to which the present invention pertains will understand that the present invention may be embodied in other specific forms without changing the technical spirit or essential features thereof. will be able Therefore, it should be understood that the embodiment described above is illustrative in all respects and not restrictive.

Claims (6)

Collecting seawater composed of deep coastal bedrock water,
The first seawater is prepared by filtering and removing foreign substances or solids deposited in the collected seawater with a filter, but as the filter, sand filter, activated carbon filter, micro filter And filters that combine any one or more selected from the group consisting of ultra filtration (Ultra filter) are used,
After mixing and storing the pure git powder in the first seawater, the pure git powder and the precipitated foreign substances or solids are filtered and removed with a filter to prepare second seawater,
After mixing the microporous body with the second seawater, the third seawater is prepared by first heating to evaporate moisture, and separating and collecting only the liquid using a filter,
After cooling and crystallizing the third seawater, it is filtered through a filter to remove solids to prepare ionized water,
In the step of preparing the second seawater by mixing and storing the pure git powder in the first seawater, and then filtering and removing the pure git powder and the precipitated foreign substances or solids with a filter, the total content of the first seawater is 100 parts by weight. After mixing in a weight ratio of 1 to 5 parts by weight of the pure jit powder, it proceeds by maintaining at a temperature of 20 to 40° C. for 1 to 3 days,
The pure jit powder is prepared and then washed to remove the foreign substances attached to the pure git mineral, and the washed pure git mineral is first pulverized to prepare a pure jit granulated product, and the pure jit mineral is prepared. The coarsely pulverized product is immersed in a mixture consisting of 0.2 to 0.4 wt% of nitric acid, 0.5 to 1.0 wt% of a phosphate compound, 0.01 to 0.05 wt% of a persulfate, 1 to 3 wt% of acetic acid, and the remainder of purified water for 20 to 40 minutes, and the After separating and taking out the raw material granulated powder from the mixed solution, the raw material granulated raw material is put into a kiln and heated for 50 to 100 minutes at a temperature of 1,100 to 1,300 ° C. A second pulverization to 10 to 100 nm is performed to prepare a pulverized pure jit, and the pulverized pulverized pure jite is put into a rotary tub equipped with a magnet, and then rotated at a rotation speed of 500 to 1000 RPM for 10 to 20 minutes to remove impurities. It is manufactured through a process of removal and sterilization,
In the step of preparing the third seawater by mixing the microporous body with the second seawater, evaporating the moisture by first heating, and collecting only the liquid by using a filter, the microporous body with respect to 100 parts by weight of the total content of the second seawater After mixing in a weight ratio of 1 to 5 parts by weight, the third seawater is prepared by heating at a temperature of 80 to 85 ° C. for 5 to 10 hours,
The microporous body, but prepare unburned carbon powder, fly ash, loess, dredged soil and water, the unburned carbon powder, fly ash, loess and dredged soil are each unburned carbon powder 10 to 15 parts by weight, fly ash 8 to 12 parts by weight, loess 2 It is prepared in a weight ratio of 4 to 4 parts by weight and 3 to 7 parts by weight of dredged soil, and the water is prepared in a weight ratio of 30 to 40 parts by weight based on 100 parts by weight of the total unburned carbon powder, fly ash, loess and dredged soil, the unburned carbon powder , After preparing a mixture by mixing fly ash, loess, dredged earth and water, the mixture is molded into a spherical shape to form a molded body, and the molded body is heated in a kiln and heated to sinter, wherein the kiln has an internal temperature of 400 to Maintaining at a temperature of 450 ℃, after putting the molded body inside the kiln, it is fired for 3 to 5 hours while raising the temperature to 1200 to 1300 ℃, and after taking out the fired molded body from the kiln 200 to 250 ℃ After cooling for 1 to 3 hours at a temperature, it is prepared through a process of cooling at a temperature of 30 to 50 ° C. for 10 to 12 hours,
The third seawater is cooled and crystallized, and then filtered through a filter to remove solids to prepare ion water. As the filter, any one or more selected from a nano filter or a reverse osmosis filter is combined. A method for producing hypermineral ionized water, characterized in that filters are used.
delete delete Hypermineral ionized water, antler collagen, kangaroo claw extract, green tea extract, green lipped mussel oil, polydeoxyribonucleotide sodium, L-carnitine, ascorbic acid, 1,2- Hexanediol (1,2-Hexanediol), Purified Water, Palmitoyl Tripeptide-1, Hydroxyethylcellulose, Butylene Glycol, Polysorbate 20 , Sodium acetylated hyaluronate (Sodium Acetylated Hyaluronate), hydrolyzed hyaluronic acid (Hydrolyzed Hyaluronic Acid) and glycerin (Glycerin), characterized in that it comprises a cosmetic composition comprising ionized hypermineral water.
5. The method of claim 4,
The hypermineral ionized water collects seawater composed of deep coastal bedrock water, and filters foreign substances or solids deposited in the collected seawater with a filter to prepare first seawater, but with the filter, sand filter , activated carbon filtration (Activated Carbon filter), micro filtration (Micro filter) and ultra filtration (Ultra filter) are used, a combination of any one or more filters selected from the group consisting of, and the first seawater mixed with pure jit powder After storage, the pure git powder and the precipitated foreign substances or solids are filtered to remove the second seawater, and the second seawater is mixed with a microporous body, and then heated to evaporate moisture and use a filter. The third seawater is prepared by separating and collecting only the liquid, and after cooling and crystallizing the third seawater, it is filtered through a filter to remove solids to produce ionized water, characterized in that it contains hypermineral ionized water a cosmetic composition.
6. The method of claim 5,
10 to 20 parts by weight of the hypermineral ionized water, 0.001 to 0.01 parts by weight of antler collagen, 0.2 to 0.6 parts by weight of kangaroo claw extract, 0.08 to 0.12 parts by weight of seaweed extract, 0.08 to 0.12 parts by weight of green lipped mussel oil, polydeoxyribonucleotide Sodium (Polydeoxyribonucleotide Sodium) 0.08 to 0.12 parts by weight, L-carnitine 0.05 to 0.1 parts by weight, Ascorbic acid 0.05 to 0.1 parts by weight, 1,2-hexanediol (1,2-Hexanediol) 1.5 to 2.5 parts by weight, 80 to 120 parts by weight of purified water, 0.01 to 0.1 parts by weight of palmitoyl tripeptide-1, 0.008 to 0.012 parts by weight of hydroxyethylcellulose, butylene glycol (Butylene) Glycol) 0.1 to 0.5 parts by weight, Polysorbate 20 0.008 to 0.012 parts by weight, Sodium Acetylated Hyaluronate 0.001 to 0.005 parts by weight, Hydrolyzed hyaluronic acid (Hydrolyzed Hyaluronic Acid) 0.001 to 0.005 parts by weight and glycerin (Glycerin) A cosmetic composition comprising ionized hypermineral water in a weight ratio of 0.1 to 1.5 parts by weight.

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