JP2008093612A - Reaction active species containing water manufacturing method and reaction active species containing water - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a reaction active species containing water manufacturing method which can easily be carried out without giving a physical stimulus on a fine bubble in water and activating an oxidizing agent. <P>SOLUTION: Fine bubbles having a particle size of 50 μm or smaller is formed in water having an electric conductivity of 100 μS/cm or higher, and a pH of 5 or lower. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a method for producing water containing reactive active species as water having a special function that is potentially useful in all technical fields, and water containing reactive active species produced by the method.

Reactive species represented by free radical species such as hydroxyl radical (.OH) and hydrogen radical (.H) have excellent actions such as decomposition of chemical substances, sterilization of harmful microorganisms, and cleaning of interfaces. This is a fact well known to contractors. And since the water containing such reactive active species can be used for water treatment such as sewage treatment, decomposition treatment of harmful substances, chemical synthesis of various compounds, and the like, its utility value has attracted attention in recent years. The inventors of the present invention have been studying a method for producing water containing such reactive species for many years. As a result of the research, in Patent Document 1, a particle size generated in water is 50 μm or less. It reacts in water by forcibly crushing bubbles by applying physical stimuli such as discharge, ultrasonic irradiation, punching plate, etc., or by applying an oxidizing agent such as ozone or hydrogen peroxide. A method for generating active species is proposed. However, this method requires equipment and an oxidizing agent in order to give a physical stimulus. Therefore, development of a simpler method for producing water containing reactive species is desired.
International Publication No. 2005/030649 Pamphlet

  Then, this invention aims at providing the manufacturing method of the water containing the reactive active species which can be performed simply, without giving a physical irritation | stimulation with respect to the microbubble in water, or making an oxidizing agent act. To do.

The method for producing water containing the reactive species of the present invention made in view of the above points, as described in claim 1, has a particle size of 50 μm in water having an electric conductivity of 100 μS / cm or more and a pH of 5 or less. The following microbubbles are generated.
The manufacturing method according to claim 2 is characterized in that, in the manufacturing method according to claim 1, after generating microbubbles in water, the microbubbles are naturally suspended in water for at least 10 seconds.
The manufacturing method according to claim 3 is characterized in that, in the manufacturing method according to claim 1, the electrical conductivity of water that generates microbubbles is adjusted by adding an electrolyte.
The manufacturing method according to claim 4 is characterized in that, in the manufacturing method according to claim 1, the pH of water that generates microbubbles is adjusted by adding an organic acid and / or an inorganic acid.
The production method according to claim 5 is characterized in that, in the production method according to claim 1, the reactive species is a hydroxyl radical.
The method for producing reactive species in water according to the present invention, as described in claim 6, generates microbubbles having a particle size of 50 μm or less in water having an electric conductivity of 100 μS / cm or more and a pH of 5 or less. It is characterized by that.
In addition, the water containing the reactive species of the present invention, as described in claim 7, generates microbubbles having a particle size of 50 μm or less in water having an electric conductivity of 100 μS / cm or more and a pH of 5 or less. It is manufactured.
Further, according to the method for treating an oxidation target of the present invention, as described in claim 8, the oxidation target is present in water containing the reactive species of claim 7, and is oxidized by the reactive species in water. It is characterized by.

  ADVANTAGE OF THE INVENTION According to this invention, the manufacturing method of the water containing the reactive active species which can be performed simply, without giving a physical irritation | stimulation with respect to the microbubble in water or making an oxidizing agent act can be provided. .

  The method for producing water containing reactive species of the present invention is characterized in that microbubbles having a particle size of 50 μm or less are generated in water having an electric conductivity of 100 μS / cm or more and a pH of 5 or less. . Generates microbubbles with a particle size of 50 μm or less in a water tank or natural water area with a certain depth (for example, 20 cm or more), with water conductivity of 100 μS / cm or more and pH of 5 or less. In order to adjust the electrical conductivity of the microbubbles, ions in the water, such as hydroxyl ions, protons (hydrogen ions), at the gas-liquid interface, while maintaining their spherical shape under the condition of naturally floating When electrolyte is added or when the electrolyte is originally present in water, the electrolyte ion is reduced while concentrating as a charge, and at the moment of extinction, the highly concentrated charge loses the interface that causes the concentration. By doing so, the charge energy stored as an ultra-high electric field is instantly released, thereby generating reactive species. As a generation mechanism of the reactive active species, it can be considered that the water around the bubbles is forcibly decomposed by releasing the charge energy stored as an ultrahigh electric field. The water containing the reactive species produced by the method of the present invention can be used for water treatment such as sewage treatment, decomposition of harmful substances, chemical synthesis of various compounds, and the like.

  In the present invention, the method for generating microbubbles having a particle size of 50 μm or less in water is not particularly limited, and a method known per se can be employed. For example, it can be performed by stirring the gas-liquid mixture under flow. In this case, the gas acquired in the eddy current is generated by forcibly generating a vortex with a radius of 10 cm or less using a rotor and hitting the gas-liquid mixture against obstacles such as walls and fluids with different relative velocities. By dispersing the components together with the disappearance of the vortex, a large amount of desired microbubbles can be generated. Further, bubbles can be generated from the supersaturated condition of the dissolved gas generated by dissolving the gas in water under a high pressure of 2 atmospheres or more and then releasing the gas to atmospheric pressure. In this case, a large number of vortices with a radius of 1 mm or less are generated at the pressure release site using water flow and obstacles, and a large amount of gas phase nuclei (bubble nuclei due to water molecular fluctuations in the central region of the vortex flow. ), And by diffusing gas components in water toward these bubble nuclei along with the supersaturation condition to grow the bubble nuclei, a large amount of desired microbubbles can be generated. The concentration of the bubbles generated by these methods is 100 / mL or more, and it is not rare that the value is higher than 1000 / mL (see Japanese Patent Application Laid-Open No. 2000-51107 or specially if necessary). (See, eg, Japanese Unexamined Patent Publication No. 2003-265938).

  It is desirable to adjust the electrical conductivity of water that generates microbubbles by adding an electrolyte as necessary. As the electrolyte, sodium chloride, hydrochloric acid, sulfuric acid, nitric acid, or the like can be used. By changing the type of electrolyte to be used, the type of reactive active species to be generated can be changed.

  It is desirable to adjust the pH of water that generates microbubbles by adding an organic acid and / or an inorganic acid as necessary. As the organic acid, acetic acid, oxalic acid, citric acid, or the like can be used. As the inorganic acid, hydrochloric acid, sulfuric acid, nitric acid or the like can be used.

  The present inventors have obtained the following knowledge regarding the present invention by studying the characteristics of microbubbles under various conditions over many years. That is, when microbubbles having a particle size of 50 μm or less are generated in water, hydroxyl ions and protons accumulate at the gas-liquid interface of the bubbles. This is related to structural factors possessed by water, and in particular, hydroxyl ions tend to accumulate. This tendency is expressed as the zeta potential of microbubbles as shown in FIG. 1 (details on this phenomenon are published in the literature by the inventor, for example, Journal of Physical Chemistry B 109-46, pp21858-21864, ζ (See Potential of Microbubbles in Aqueous Solutions: Electrical Properties of the Gas-Water Interface, M. Takahashi, etc.). In addition, when an electrolyte is added to adjust the electrical conductivity or when the electrolyte originally exists in water, electrolyte ions are attracted to the periphery of the interface by the electrostatic force according to the charge at the gas-liquid interface, so-called electric double layer And the effect of the charge on the surroundings is local. In this way, the microbubbles are surrounded by hydroxyl ions, protons and surrounding electrolyte ions, but these ions do not significantly limit the dissolution of the gas from the bubbles, so the bubbles dissolve the gas inside. To reduce the surface area rapidly. The accompanying reduction in the bubble particle size strongly pressurizes the internal gas based on Young's Laplace law. The pressurized gas dissolves in the water around the bubble according to Henry's law, so the bubble eventually disappears in the water while increasing the shrinkage rate (details on this phenomenon are described in the literature published by the inventors, for example, , Journal of Physical Chemistry B 107-10, pp2171-2173, Effect of Shrinking Microbubble on Gas Hydrate Formation, M. Takahashi, et.al.

Now, when the reduction rate of the bubble particle diameter exceeds 0.5 μm / sec under the above conditions, the moving speed of the gas-liquid interface becomes significantly faster than the diffusion rate of the electrolyte ions in water, and the escape is not complete. We discovered for the first time in the world that the electrolyte ions disappeared and began to concentrate at the gas-liquid interface. Under the absolute condition that microbubbles maintain a spherical shape, this concentration rate tends to increase as the bubble diameter decreases, and in water where the electrical conductivity is 100 μS / cm or more and the pH is 5 or less. At the moment of the final bubble disappearance, a very unique ultrahigh electric field is formed so that the surface potential of the gas-liquid interface is expected to exceed 1000V. The only technique that can keep the bubbles in the shrinking process to be spherical until the end is natural standing by natural floating. Since there is no physical stimulus under the condition of natural standing, the spherical bubbles are not deformed and form a surface charge condition necessary for the generation of reactive active species without breaking through a reduction process due to the internal pressurizing effect. From the above viewpoint, it is desirable that the microbubbles are naturally floated in the water for at least 10 seconds after the microbubbles are generated in the water. Note that the normal flow of microbubbles and the parallel movement in the pipes do not give physical stimulation to the microbubbles. Therefore, even in these systems, the electrical conductivity is 100 μS / cm or more and the pH is high. If microbubbles having a particle size of 50 μm or less can be generated in water of 5 or less, the generated microbubbles contribute to the generation of reactive species.

  A feature of the present invention is that it uses the formation of an ultra-high electric field accompanying the reduction process of microbubbles to generate reactive species, which includes physical stimulation such as discharge, ultrasonic irradiation, and punching plate passing. This is greatly different from the method of generating reactive species using the extreme reaction field.

  EXAMPLES Hereinafter, although an Example demonstrates this invention in detail, this invention is limited to the following description and is not interpreted.

Example 1:
For example, according to the method described in Japanese Patent Application Laid-Open No. 2003-265938, after dissolving air in water having an electric conductivity of 100 μS / cm or more and a pH of 5 or less under a high pressure of 4 atm, this is released to atmospheric pressure. Microbubbles having a particle size of 50 μm or less were generated from the supersaturated condition of the dissolved air generated by this, and this was collected in a beaker. The electrical conductivity and pH of water were adjusted by adding sulfuric acid. After adding DMPO (5,5-dimethyl-1-pyrroline-N-oxide), which is a spin trapping agent, to a beaker, it is allowed to stand for a while on the table without any physical stimulus, By keeping the conditions, reactive species were generated in water. The reactive species generated by the above method were measured by electron spin resonance (ESR). FIG. 2 shows the spectrum of reactive species analyzed by ESR after the microbubbles disappear. As is clear from FIG. 2, from this spectrum, four peaks having a size of 1: 2: 2: 1 characteristic of the hydroxyl radical are recognized, and the hydroxyl radical is generated as a reactive species. all right. Since the hydroxyl radical is one of the strongest oxidizing agents in water, it has been found that according to this method, various chemical substances can be oxidatively decomposed using the hydroxyl radical generated in water.

Example 2:
Using a well-known microbubble generator (see JP-A-2003-265938 if necessary), a 5 L container filled with phenol at a concentration of 1.5 mM has an electric conductivity of 100 μS. Microbubbles having a particle size of 50 μm or less were generated in water having a pH of 5 or less and a / cm or more. The electrical conductivity and pH of water were adjusted by adding nitric acid. The supplied gas was air, and the supply amount was about 2 L / min. The generated fine bubbles had an average particle size of about 10 μm and a concentration of bubbles of about 2000 / L. For the convenience of continuously generating microbubbles, the pump continued to be driven, but the circulation rate was about 8 L / min, and more than 50% of the microbubbles released into the container were at least 10 seconds away from the pump. It was placed in the condition of natural floating without receiving physical stimulation accompanying driving. FIG. 3 shows the results of examining how the concentration of phenol added to water changes after the microbubble generator is activated. As is apparent from FIG. 3, the phenol was able to be decomposed by about 30% by operating the microbubble generator for 3 hours. Along with this, the formation of formic acid, oxalic acid, etc. was recognized in addition to benzoquinone, which is a phenol decomposition intermediate. The above results show that, as shown in Example 1, the microbubbles shrink while maintaining a spherical shape in the process of natural floating, and the charge concentrated to a high concentration at the moment of disappearance loses the interface that causes the concentration. Thus, it is considered that the charge energy stored as an ultrahigh electric field is instantaneously released, whereby a hydroxyl radical is generated as a reactive species, and the generated hydroxyl radical oxidizes and decomposes phenol. In addition, when the electrical conductivity of water was less than 100 μS / cm or when the pH was higher than 5, no decomposition of phenol occurred.

  The present invention is able to provide a method for producing water containing reactively active species, which can be easily carried out without giving physical stimulation to microbubbles in water or allowing an oxidizing agent to act. Has industrial applicability.

It is a conceptual diagram which shows distribution of ions in the gas-liquid interface of a microbubble. 2 is an ESR spectrum of a hydroxyl radical as a reactive species generated in Example 1. FIG. It is a graph which shows the time transition of the phenol decomposition | disassembly in Example 2. FIG.

Claims (8)

  A method for producing water containing reactive species, wherein microbubbles having a particle size of 50 µm or less are generated in water having an electric conductivity of 100 µS / cm or more and a pH of 5 or less.   2. The production method according to claim 1, wherein the microbubbles are naturally suspended in water for at least 10 seconds after the microbubbles are generated in the water.   The manufacturing method according to claim 1, wherein the electric conductivity of water for generating microbubbles is adjusted by adding an electrolyte.   2. The production method according to claim 1, wherein the pH of water for generating microbubbles is adjusted by adding an organic acid and / or an inorganic acid.   The production method according to claim 1, wherein the reactive species is a hydroxyl radical.   A method for producing reactive species in water, wherein microbubbles having a particle size of 50 µm or less are generated in water having an electric conductivity of 100 µS / cm or more and a pH of 5 or less.   Water containing reactive species characterized by being produced by generating microbubbles having a particle size of 50 µm or less in water having an electric conductivity of 100 µS / cm or more and a pH of 5 or less.   A method for treating an oxidation target, comprising causing an oxidation target to exist in water containing the reactive active species according to claim 7, and oxidizing the reactive active species in water.