ONE-SOLUTION TYPE PHOTOCATALYST-CONTAINING COATING SUSPENSION AND METHOD OF PREPARING THE SAME
20180282552 ยท 2018-10-04
Assignee
Inventors
Cpc classification
C09D1/00
CHEMISTRY; METALLURGY
B01J21/063
PERFORMING OPERATIONS; TRANSPORTING
B01J37/0009
PERFORMING OPERATIONS; TRANSPORTING
International classification
B01J21/06
PERFORMING OPERATIONS; TRANSPORTING
B01J37/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
There is provided one-solution type photocatalyst-containing coating suspension comprising: 100 parts by weight of an aqueous solution including deionized water; 2 to 15 parts by weight of photocatalyst powders, wherein each of the photocatalyst powders receives light from an outside and exhibits a photocatalytic effect; 10 to 20 parts by weight of a negatively charged surfactant, wherein the surfactant surrounds the photocatalyst powders such that the photocatalyst powers are micellized into micelles dispersed in the aqueous solution; 5 to 15 parts by weight of colloidal inorganic binders dispersed in the aqueous solution.
Claims
1. One-solution type photocatalyst-containing coating suspension comprising: 100 parts by weight of an aqueous solution including deionized water; 2 to 15 parts by weight of photocatalyst powders, wherein each of the photocatalyst powders receives light from an outside and exhibits a photocatalytic effect; 10 to 20 parts by weight of a negatively charged surfactant, wherein the surfactant surrounds the photocatalyst powders such that the photocatalyst powers are micellized into micelles dispersed in the aqueous solution; 5 to 15 parts by weight of colloidal inorganic binders dispersed in the aqueous solution.
2. The suspension of claim 1, wherein when the photocatalyst powders absorb light energy of a given wavelength, electrons (e) and holes (h+) are generated in the photocatalyst powders, wherein the electrons and the holes enable a material contacting the photocatalyst powders to undergo a redox reaction, wherein the photocatalyst powders include semi-conductive metal oxides or sulfur compound.
3. The suspension of claim 2, wherein the photocatalyst powders include at least one selected from a group consisting of ZnO, WO3, SnO2, ZrO2, TiO2, CdS, and CdSe.
4. The suspension of claim 3, wherein the photocatalyst powders include titanium dioxide (TiO2).
5. The suspension of claim 4, wherein titanium dioxide (TiO2) includes a combination of anatase and rutile forms thereof in a ratio of 2:8 to 8:2.
6. The suspension of claim 3, wherein the surfactant micellizes the photocatalyst powders so as to suppress contacts between the photocatalyst powders and the binders.
7. The suspension of claim 3, wherein the negatively charged surfactant includes at least one selected from a group consisting of sodium stearate, sodium dodecyl sulfate, sodium dodecylbenzenesulfonate, sodium laureth sulfate, sodium lauroyl sarcosinate, sodium myreth sulfate, and sodium pareth sulfate.
8. The suspension of claim 1, wherein the inorganic binders are present in the form of a colloid in the aqueous solution, wherein when a mixture of an initiator and the one-solution type photocatalyst-containing coating suspension is applied on a target object, moisture is gradually evaporated from a surface of the object, and, thus, the inorganic binder gradually exhibits an adhesive force.
9. The suspension of claim 1, wherein the inorganic binder includes a porous zeolite-based binder, or includes a silicon-based binder having SiO bonds having a larger binding energy on a main chain thereof.
10. A method for producing one-solution type photocatalyst-containing coating suspension, the method comprising: providing 100 parts by weight of an aqueous solution including deionized water; adding into the aqueous solution 2 to 15 parts by weight of photocatalyst powders and 10 to 20 parts by weight of a negatively charged surfactant, to form a first mixture wherein each of the photocatalyst powders receives light from an outside and exhibits a photocatalytic effect; stirring the first mixture such that the photocatalyst powers are micellized into micelles using the surfactant, wherein the micelles are dispersed in the aqueous solution to form a first suspension; and adding and stirring 5 to 15 parts by weight of colloidal inorganic binders into the first suspension, thereby to form the photocatalyst-containing coating suspension in which the micelles and the binders are dispersed uniformly.
11. The method of claim 10, further comprising adjusting pH of the first suspension to a range of pH 7 to pH 10 for stabilization of the first suspension.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0037]
[0038]
DETAILED DESCRIPTION
[0039] Examples of various embodiments are illustrated and described further below. It will be understood that the description herein is not intended to limit the claims to the specific embodiments described. On the contrary, it is intended to cover alternatives, modifications, and equivalents as may be included within the spirit and scope of the present disclosure as defined by the appended claims.
[0040] According to the present disclosure, a photocatalyst-containing coating suspension includes 100 parts by weight of an aqueous solution including deionized water. As the above-mentioned aqueous solution, water generally used may be used. Preferably, deionized water may be used.
[0041] According to the present disclosure, the one-solution type photocatalyst-containing coating suspension comprises 2 to 15 parts by weight of a photocatalyst material that receives light from the outside and exhibits a photocatalytic effect.
[0042] When the light energy of a certain wavelength is applied to the photocatalyst material, a large amount of electrons (e) and a large amount of holes (h+) are generated in the material. Thus, the redox reaction is caused by the electrons and the holes in various materials existing nearby the photocatalyst material. As the photocatalyst material, semiconductive metal oxides may be exemplified. More specifically, ZnO, WO.sub.3, SnO.sub.2, ZrO.sub.2, TiO.sub.2, CdS, CdSe and the like may be exemplified. It is preferable that the photocatalyst material is processed into a fine powder. This is because when the powder is processed into a fine powder, its surface area may be widened and a reaction portion may be increased. A size of the fine powder is preferably in a range commonly used in this technical field. Such fine powders may be readily purchased and used by those skilled in the art.
[0043] Among the above photocatalyst materials, titanium dioxide (TiO.sub.2) may be used in accordance with the preferred embodiment of the present disclosure. Titanium dioxide (TiO.sub.2) exists in three following forms: anatase form, rutile form, and brookite form, depending on crystal arrangement. Among the forms, widely used and actually available forms are anatase form and rutile form. This is because that the rutile type has the most stable state of TiO.sub.2, and the anatase form may be easily crystallized at low temperatures. The anatase form has good surface activity and is sensitive to the photoactive reaction. The rutile form has the advantages of good white brightness and hiding ability.
[0044] According to the present disclosure, the crystalline forms may be used singly or in combination with each other. The latter case may be advantageous because it is often more efficient to mix the forms appropriately depending on use environments thereof. According to the present disclosure, when the forms are mixed with each other, it is preferable to mix the anatase form and rutile form in a ratio of 2:8 to 8:2. The mixing ratio may be specifically determined in consideration of the properties of the anatase form and the rutile form based on a given environment.
[0045] The photocatalyst material is preferably used in an amount of 2 to 15 parts by weight based on 100 parts by weight of the aqueous solution. When the photocatalyst material is used in an amount of less than 2 parts by weight, the content thereof is too small to exert a photocatalytic effect. On the other hand, when the photocatalyst material is contained in an amount exceeding 15 parts by weight, the degree of increase of the photocatalytic effect is not proportional to the added amount thereof, and accordingly, the amount of the surfactant to be added is increased, which is not preferable.
[0046] According to the present disclosure, the one-solution type photocatalyst-containing coating suspension comprises 10 to 20 parts by weight of a negative charged surfactant which micellizes the photocatalyst material in the aqueous solution.
[0047] The negative charged surfactant is added to micellize the photocatalyst material dispersed in the aqueous solution. When the negative charged surfactant is contained in the aqueous solution in an amount exceeding 10 parts by weight based on 100 parts by weight of the aqueous solution, the surfactant surrounds the photocatalyst material dispersed in the aqueous solution, and, thus, gradually micellizes the photocatalyst material. Therefore, when the negative charged surfactant is contained in an amount of less than 10 parts by weight based on the weight of the aqueous solution, micelle formation is difficult. On the other hand, when the negative charged surfactant is contained in an aqueous solution in an amount of more than 20 parts by weight based on 100 parts by weight of the aqueous solution, an excessive amount of the surfactant may suppress the colloid formation, which is undesirable.
[0048] The negative charged surfactant may be used without limitation as long as it encapsulates the photocatalyst material and micellizes it. According to the present disclosure, by micellizing the photocatalyst material, the photocatalyst material is not bonded to an inorganic binder component to be added later in the aqueous solution. In other words, micelles resulting from the micellization of the photocatalyst material using the negative charge surfactant may serve as a blocking layer which basically prevents the photocatalyst material from reacting with the external inorganic binder component.
[0049] As the negative charged surfactant, typically, sodium stearate and sodium dodecyl sulfate are most preferred. In addition, surfactants such as sodium dodecylbenzenesulfonate, sodium laureth sulfate, sodium lauroyl sarcosinate, sodium myreth sulfate, and sodium pareth sulfate may be used.
[0050] According to the present disclosure, the one-solution type photocatalyst-containing coating suspension comprises 5 to 15 parts by weight of a colloidal inorganic binder dispersed in the aqueous solution.
[0051] The colloidal inorganic binder refers to a binder component of the inorganic material existing in a colloidal state inside the aqueous solution. The inorganic binder is present in the form of a colloid in the aqueous solution. However, when an initiator such as water is added to the one-solution type photocatalyst-containing coating suspension, and the composition is applied to the surface of the target object, moisture is gradually evaporated from the surface of the object, and, thus, the inorganic binder gradually exhibits an adhesive force.
[0052] The colloidal inorganic binder may be a zeolite-based binder which is not easily decomposed by the photocatalytic effect unlike the organic binder.
[0053] The inorganic binder may include a porous zeolite-based binder, or may include a silicon-based binder having SiO bonds having a large binding energy between elements on the main chain. Since the inorganic binder must be dispersed in a stable state in the aqueous solution, the inorganic binder is preferably formed in a colloidal form.
[0054] When the colloidal inorganic binder is contained in an amount of less than 5 parts by weight based on 100 parts by weight of the aqueous solution, the inorganic binder content is not preferable because of the weak adhesive force of the binder when the present coating suspension is applied to the object to be coated. On the contrary, when the inorganic binder is contained in an amount exceeding 15 parts by weight, the stability of the aqueous solution may be deteriorated due to the excessive content of the binder, which is not preferable. As the colloidal inorganic binder, for example, colloidal-phase porous silica or aluminosilicate is most preferable.
[0055] Furthermore, in accordance with the present disclosure, there is provided a method for producing the one-solution type photocatalyst-containing coating suspension as described above.
[0056] A method for manufacturing the one-solution type photocatalyst-containing coating suspension according to the present disclosure includes a first step for adding 2 to 15 parts by weight of a photocatalyst material which receives light from the outside and exhibits a photocatalytic effect and 10 to 20 parts by weight of a negative charged surfactant into 100 parts by weight of the aqueous solution including deionized water, and then dispersing the photocatalyst material and the surfactant in the aqueous solution uniformly to form a suspension.
[0057] According to the present disclosure, 2 to 15 parts by weight of the photocatalyst material is added to 100 parts by weight of the aqueous solution of deionized water and is dispersed uniformly in the solution. The photocatalyst material may be finely pulverized and may be weighed and commercially purchased from the market. In order to uniformly disperse the photocatalyst material in the solution, a mixing process may be performed uniformly, and ultrasound treatment may be supplementarily performed, if necessary.
[0058] According to the present disclosure, 10 to 20 parts by weight of the negatively charged surfactant is added to 100 parts by weight of the above aqueous solution in which the photocatalyst component is uniformly dispersed, thereby to form a first mixture. Then, the first mixture is uniformly stirred to obtain a uniformly dispersed suspension. At this time, the suspension contains a plurality of micelles dispersed in a colloidal form therein, each micelle being formed of the photocatalyst component surrounded by the surfactant.
[0059] According to the present disclosure, after the suspension having the micelles of the photocatalytic material and the negatively charged surfactant dispersed therein is slowly stirred, the pH of the suspension is adjusted to a range of 7 to 10 for the stabilization of the suspension. This pH adjustment may be achieved using sodium hydroxide (NaOH).
[0060] According to the present disclosure, the method for manufacturing the one-solution type photocatalyst-containing coating suspension according to the present disclosure includes a second step for adding 5 to 15 parts by weight of the colloidal inorganic binder component to the water-soluble suspension containing the colloidal micelles and the negatively charged surfactant therein to form a second mixture, and uniformly dispersing the binder, the micelles and the surfactant in the second mixture.
[0061] According to the present disclosure, 5 to 15 parts by weight of the above-mentioned colloidal inorganic binder component based on 100 parts by weight of the aqueous solution is added to the aqueous suspension to prepare the suspension, and the suspension is uniformly stirred such that the binder, the micelles and the surfactant are uniformly dispersed in the suspension.
[0062] When the colloidal inorganic binder component is introduced into the aqueous suspension, the inorganic binder component is dispersed in the suspension as it is in non-contact with the photocatalyst powder. This is because the photocatalyst powder is already micellized and cannot physically contact the inorganic binder.
[0063] Hereinafter, a preferred example of the present disclosure will be described.
Example
[0064] A 2-liter vessel was prepared. Then, in the vessel, 100 g of titanium dioxide (TiO.sub.2) was introduced into 1000 g of deionized water to form a first mixture. Then, the first mixture was stirred slowly. Then, 150 g of sodium dodecyl sulfate was added to the first mixture to form a second mixture, which was continuously stirred for 1 hour.
[0065] With continued stirring of the second mixture, 120 g of colloidal silica was added to the second mixture in the vessel to form a third mixture which was then stirred for a further 30 minutes. Thus, a reaction solution was obtained as a final suspension.
[0066] The thus-prepared one-solution type photocatalyst-containing coating suspension maintains a stable state of the suspension. Therefore, after the water as the initiator is mixed with the suspension solution to form a mixture, the mixture is applied to the surface of the target object, or sprayed or thin-filmed. As the water evaporates from the photocatalyst-containing coating suspension applied on the surface of the object, the inorganic binder component in the colloidal state gradually comes into contact with the surface of the object and exhibits the adhesion. At this time, when the worker pours water on the surface of the object and rinses it, the micelle structure is destroyed, and the surfactant existing around the micelle is dissolved in water and, thus, washed away from the object together with water.
[0067]
[0068] Therefore, the photocatalyst material is fixed to the surface of the object by the inorganic binder component on a bottom side of the photocatalyst material. However, on a top side of the photocatalyst material, the surface active agent or surfactant is dissolved in the water and is washed away from the object together with water. Thus, on the top side of the photocatalyst material, open sections may formed. Through the open section, the photocatalyst material may freely contact outside air or room air.
[0069] On the contrary, when using a conventional two-solution type photocatalyst-containing coating suspension, the photocatalyst material is surrounded by the inorganic binder component on the surface of the target object. Therefore, reduction in the photocatalytic effect may be worsened as much as the photocatalyst material is surrounded by the inorganic binder component.
[0070]
[0071] The one-solution type photocatalyst-containing coating suspension according to the present disclosure and its preparation method have been above described in detail. However, the present disclosure is not limited thereto. The scope of the present disclosure may be defined by following claims and their equivalents.
[0072] It will be apparent to those skilled in the art that various changes and modifications may be made by those skilled in the art without departing from the spirit and scope of the disclosure as defined by the appended claims.