The present invention relates to ceramics, more particularly to a method for treating a glazed ceramic article with an antimicrobial.
It is known to add minerals to a ceramic glaze to produce a glaze with antimicrobial properties. Minerals having an antimicrobial effect are mixed with the glaze prior to application on a ceramic body and then fired to become a permanent part of the ceramic surface.
However, adding minerals having an antimicrobial effect to the ceramic glaze often causes defects and alters texture, color, and other properties. Any and all inorganic minerals added to a ceramic glaze prior to firing will have some effect on the final properties of the glaze. Minerals that will impart antimicrobial effect often negatively impact desired color and texture properties of the glaze. The properties most often affected are color, texture, and slip resistance (i.e. surface roughness).
For example, the zinc level in a glaze affects an antimicrobial addition. Zinc fluxes, which causes more melting, in high temperature glazes. There are also interactions with pigments which often affects color.
Also, since many antimicrobial additives are expensive minerals, combining these into a relatively thick glaze layer adds significant cost. Furthermore, much of the minerals having an antimicrobial effect are lost in the depth of the glaze where it cannot affect any bacteria on the surface.
Thus, there is a need for an alternative method that overcomes the disadvantages associated with known methods.
The invention provides a method for surface application of minerals having an antimicrobial effect on glazed ceramics.
In an embodiment of the invention, a method of treating a glazed ceramic article with an antimicrobial is provided. The method comprises applying an antimicrobial composition on top of an outermost surface of a glazed ceramic article, wherein the antimicrobial composition comprises an antimicrobial additive.
In an embodiment of the invention, a treated glazed ceramic article is provided. The treated glazed ceramic article comprises a glazed ceramic article having an outermost surface, and an antimicrobial composition on top of the outermost surface of the glazed ceramic article. The antimicrobial composition comprises an antimicrobial additive, preferably selected from the group consisting of Bi2O3, ZnO, Ag2CO3, Ag2O, Zn, Bi, Ag, and a combination thereof.
Further areas of applicability of the present invention will become apparent from the detailed description provided hereinafter. It should be understood that the detailed description and specific examples, while indicating the preferred embodiments of the invention, are intended for purposes of illustration only and are not intended to limit the scope of the invention.
The present invention will become more fully understood from the detailed description and the accompanying drawings, which are not necessarily to scale, wherein:
The following description of the embodiments of the present invention is merely exemplary in nature and is in no way intended to limit the invention, its application, or uses. The present invention has broad potential application and utility, which is contemplated to be adaptable across a wide range of industries. The following description is provided herein solely by way of example for purposes of providing an enabling disclosure of the invention, but does not limit the scope or substance of the invention.
As used herein, the terms “microbe” or “microbial” should be interpreted to refer to any of the microscopic organisms studied by microbiologists or found in the use environment of a ceramic article or ceramic-glazed article. Such organisms include, but are not limited to, bacteria and fungi as well as other single-celled organisms such as mold, mildew and algae. Viral particles and other infectious agents are also included in the term microbe.
As well, “antimicrobial” and like terms should be interpreted as encompassing both microbe-killing as well as microbistatic activities. That is, it herein is considered efficacious if an antimicrobial composition reduces the number of microbes on a substrate or it the composition retards the normal rate of microbial growth.
For ease of discussion, this description uses the terms microbes and antimicrobial to denote a broad spectrum activity (e.g. against bacteria and fungi). When speaking of efficacy against a particular microorganism or taxonomic rank, the more focused term will be used (e.g. antifungal to denote efficacy against fungal growth in particular).
Using the above example, it should be understood that efficacy against fungi does not in any way preclude the possibility that the same antimicrobial composition demonstrates efficacy against another class.
For example, discussion of the strong bacterial efficacy demonstrated by a disclosed embodiment should not be read to exclude the embodiment from also demonstrating antifungal activity. This method of presentation should not be interpreted as limiting the scope of the invention in any way.
In an embodiment of the present invention, the method comprises applying an antimicrobial composition comprising an antimicrobial additive or package of antimicrobial additives on top of the outermost surface of a glaze on a ceramic piece before the ceramic piece is fired. During firing, the minerals in the antimicrobial package migrate into the upper layer of the glaze and become permanently combined with the glaze. The method results in an antimicrobial additive package diffusing into the body of the glaze. The highest concentration is at the surface. The concentration diminishes through the depth of the glaze.
In an embodiment of the invention, the antimicrobial additive package diffuses into the body of the glaze according to Fick's Second Law of Diffusion, where the concentration and depth of the migration is proportional to the firing time at high temperature.
Fick's Second Law of Diffusion is:
in which the accumulation, dC/dt [cm−3 s−1], is proportional to the diffusivity [cm2/s] and the 2nd derivative (or curvature) of the concentration, [cm−3 cm−2] or [cm−5].
The highest concentration still remains at the surface of the glaze, where it is most efficacious against bacteria.
In an embodiment of the invention, the antimicrobial additive includes, but is not limited to, one or more of the following: Bi2O3, ZnO, Ag2CO3, Ag2O, or a frit comprising one or more of Zn, Bi, and Ag. As used herein, “fritting” means melting an antimicrobial agent(s) or constituent(s) into a glass, quenching the glass to freeze the amorphous condition, and then grinding to a desired particle size. A fritted antimicrobial composition is a more homogeneous composition and allows higher amounts of the components than is acceptable in the oxide form.
In an embodiment of the invention, the antimicrobial additive is a combination of 30 to 70 weight % ZnO, 30 to 70 weight % Bi2O3, and 0 to 10 weight % frit containing Ag.
The application level of antimicrobial additive on the glazed ceramic article is preferably 0.5 g/m2 to 5.0 g/m2, more preferably 1.0 g/m2 to 3.0 g/m2. The materials used are chosen based on the glaze chemistry and glaze type. Glaze chemistry is largely determined by firing temperature and product type. For example, glossy glazes use different chemistry than matte. For example, porcelain glazes use different chemistry than monoporosa, or “ceramic” tile with a porous body. Glaze type generally refers to glossy or matte, wall tile, floor tile, sanitary ware, etc. Different products require specific fired properties, such as strength, hardness, gloss, scratch resistance, and slip resistance.
In an embodiment of the invention, the antimicrobial material is applied in the same manner as glazes. Examples of application methods for use in the invention include, but are not limited to, spray, rotocolor (silicon roller), disc cabin, inkjet, or other printing method.
The antimicrobial material can be mixed with a carrier medium to form an antimicrobial composition that allows for ease of application. Examples of carrier mediums include, but are not limited to, water, polyethylene glycol, and a combination thereof. The choice of carrier medium is not critical to the fired effect as it dries or burns off. The antimicrobial composition of the invention typically has a lower ratio of solids to liquid than a glaze. In an embodiment of the invention, the antimicrobial additive is present in the antimicrobial composition in a ratio of solids to carrier medium in a range of 1% to 10%.
The amount of antimicrobial additive present in the antimicrobial composition varies by the application method. For example, if spraying tends to apply about +/−100 g/m2, which is the total wet application of what is sprayed (as dictated by the limits of the equipment), in order to get a 2 g/m2 dry weight application of antimicrobial additive then 2% is the percent solids in the composition to be sprayed.
For example, if rotocolor tends to apply about +/−30 g/m2, then 6% to 7% is the percent solids in the composition to be sprayed in order to obtain about a 2 g/m2 dry weight application of antimicrobial additive. For example, if a typical spray booth or disc cabin applies +/−100 g/m2 total weight of wet antimicrobial composition, then in order to obtain a 2.5 g/m2 dry weight application of antimicrobial additive, an antimicrobial composition is prepared at 2.5% ratio of solids to carrier medium.
In an embodiment of the invention, the method comprises applying a layer of an antimicrobial composition comprising an antimicrobial additive package(s) and a carrier medium to the surface of the ceramic glaze of a ceramic piece.
In an embodiment of the invention, the antimicrobial composition is applied on top when the glaze layer is thick so as to minimize the amount of antimicrobial. Glazes applied typically range from 15 g/m2 to 1500 g/m2 in thickness, although thickness may vary.
The antimicrobial composition can be applied in a layer of any thickness. However, preferably the antimicrobial composition is applied in a layer having a thickness in a range of 0.5 g/m2 to 5.0 g/m2.
The method further comprises firing the surface of the ceramic glaze having the antimicrobial composition applied thereon. Once fired, this layer becomes a permanent part of the ceramic glaze surface but with a higher concentration of antimicrobial minerals at the surface than throughout the glaze layer, where it is useful to resist bacterial growth. By applying the antimicrobial minerals in accordance with the method of the invention, fewer antimicrobial minerals are used which imparts less impact on the aesthetic and functional properties of the glaze, while still achieving similar or better antimicrobial efficacy.
Thus, the method of the invention overcomes the problem of applying antimicrobial minerals onto a glazed ceramic surface without creating substantial detrimental impact to the normal aesthetic and functional properties of the glaze.
An advantage of the method of the present invention is that it is less expensive and less wasteful, but no less effective, then having high value antimicrobial minerals throughout a glaze layer, where most of it is ineffective as only the top few microns of the glaze surface can interact with bacteria. The method of the invention reduces or eliminates such defects.
Another advantage is that the method of the invention allows for more versatility in production, since the same antimicrobial mixture can be used on multiple glazes, or not at all, without changing the other materials being used.
Antimicrobial efficacy data showed that efficacy is as good as or better with the application method of the invention than when antimicrobial treatment was added in the glaze. Formulation A was 33% ZnO, 66% Bi2O3, and 1% frit containing Ag.
E. Coli
Additionally, in this case, the additive of Formulation A caused the texture of the glazed porcelain tile to be smoother than desired, decreasing the slip resistance. By applying the antimicrobial on top of the glaze, the amount of antimicrobial additive was be reduced by 57.6% without a reduction in efficacy.
To demonstrate that the antimicrobial did migrate into the glaze layer during firing, two sample sets made at a porcelain tile factory were tested by removing the surface of the tile via polishing with a high speed, diamond surface polishing wheel. 0.05 mm of depth was removed from the surface of each tile sample.
These tile were then scanned with the XRF, and tested for antibacterial efficacy using ASTM E3031-15 test protocol that used on all ceramic tile. The results of those tests were as follows:
E. Coli
These results show that the tile treated in accordance with the invention with Formulation B showed excellent antimicrobial efficacy with 0.05 mm of surface removed. Formulation B was 66% ZnO, 33% Bi2O3, and 1% frit containing silver. In fact, at this depth the decorative printing had been removed.
XRF Data is as follows:
As these numbers show, the total amount of antimicrobial (AM) additive measured by XRF decreased; however, it was still present and effective in the glaze at the depth of 0.05 mm.
It has been determined from testing the antimicrobial treated tile glazes that an antimicrobial formulation when applied to the surface of the glaze and fired onto the tile, diffused into the mass of the glaze. This diffusion followed Fick's Second Law of Diffusion, where the depth of penetration was a function of the time at high temperature during firing. XRF data from this test and other similar tests confirmed this assessment.
It will therefore be readily understood by those persons skilled in the art that the present invention is susceptible of broad utility and application. Many embodiments and adaptations of the present invention other than those herein described, as well as many variations, modifications and equivalent arrangements, will be apparent from or reasonably suggested by the present invention and the foregoing description thereof, without departing from the substance or scope of the present invention. Accordingly, while the present invention has been described herein in detail in relation to its preferred embodiment, it is to be understood that this disclosure is only illustrative and exemplary of the present invention and is made merely for purposes of providing a full and enabling disclosure of the invention. The foregoing disclosure is not intended or to be construed to limit the present invention or otherwise to exclude any such other embodiments, adaptations, variations, modifications and equivalent arrangements.
Number | Name | Date | Kind |
---|---|---|---|
5252521 | Roberts | Oct 1993 | A |
5304516 | Clifford | Apr 1994 | A |
5348797 | Clough et al. | Sep 1994 | A |
5350718 | Anquetil | Sep 1994 | A |
5597644 | Araki et al. | Jan 1997 | A |
5807641 | Oku et al. | Sep 1998 | A |
5853866 | Watanabe et al. | Dec 1998 | A |
5882808 | Oku et al. | Mar 1999 | A |
6043171 | Siebers et al. | Mar 2000 | A |
6143318 | Gilchrist et al. | Nov 2000 | A |
6303183 | Wilczynski et al. | Oct 2001 | B1 |
6368668 | Kobayashi et al. | Apr 2002 | B1 |
6383646 | Tomioka et al. | May 2002 | B1 |
6514622 | Hayakawa et al. | Feb 2003 | B1 |
6756060 | Greenspan et al. | Jun 2004 | B1 |
6887812 | Nenasheva et al. | May 2005 | B2 |
7250178 | Olsson et al. | Jul 2007 | B2 |
7476698 | Wagoner et al. | Jan 2009 | B2 |
7488442 | Matsumoto et al. | Feb 2009 | B2 |
9434638 | Campbell, Jr. | Sep 2016 | B2 |
9446980 | Campbell, Jr. | Sep 2016 | B2 |
9446981 | Campbell, Jr. | Sep 2016 | B2 |
9758428 | Zhang et al. | Sep 2017 | B1 |
20030134107 | Machida et al. | Jul 2003 | A1 |
20040103823 | Kurihara et al. | Jun 2004 | A1 |
20050031703 | Beier et al. | Feb 2005 | A1 |
20050035500 | Matsumoto et al. | Feb 2005 | A1 |
20050106336 | Ong et al. | May 2005 | A1 |
20050158400 | Olsson et al. | Jul 2005 | A1 |
20050196430 | Olsson et al. | Sep 2005 | A1 |
20050249791 | Hobbs et al. | Nov 2005 | A1 |
20050252410 | Bujard et al. | Nov 2005 | A1 |
20060048676 | Bujard | Mar 2006 | A1 |
20060141015 | Tessier et al. | Jun 2006 | A1 |
20070110824 | Nageswaran | May 2007 | A1 |
20070275168 | Prochazka | Nov 2007 | A1 |
20080085326 | Ruan | Apr 2008 | A1 |
20090104459 | Campbell, Jr. | Apr 2009 | A1 |
20090117173 | Chen et al. | May 2009 | A1 |
20100204411 | Erneta et al. | Aug 2010 | A1 |
20120237686 | Chen et al. | Sep 2012 | A1 |
20130302440 | King et al. | Nov 2013 | A1 |
20140212361 | Ijaz et al. | Jul 2014 | A1 |
20140220153 | Pagotto Simões et al. | Aug 2014 | A1 |
20140271757 | Agrawal et al. | Sep 2014 | A1 |
20140356406 | Patil et al. | Dec 2014 | A1 |
20150030696 | Campbell, Jr. | Jan 2015 | A1 |
20150030861 | Campbell, Jr. | Jan 2015 | A1 |
20150030863 | Campbell, Jr. | Jan 2015 | A1 |
20150099095 | Pershin et al. | Apr 2015 | A1 |
20150359946 | Dehnad et al. | Dec 2015 | A1 |
20160081349 | Campbell, Jr. | Mar 2016 | A1 |
20160135470 | Agrawal et al. | May 2016 | A1 |
20160143291 | Campbell, Jr. | May 2016 | A1 |
20170231229 | Meier et al. | Aug 2017 | A1 |
Number | Date | Country |
---|---|---|
2279785 | Feb 2000 | CA |
1615698 | May 2005 | CN |
1843995 | Oct 2006 | CN |
19834801 | Feb 2000 | DE |
202005006784 | Sep 2005 | DE |
0190504 | Aug 1986 | EP |
H08290985 | Nov 1996 | JP |
H111380 | Jan 1999 | JP |
0014029 | Mar 2000 | WO |
2004092283 | Oct 2004 | WO |
2016094484 | Jun 2016 | WO |
Entry |
---|
International Search Report and Written Opinion of corresponding International Application No. PCT/US2017/058312; dated Dec. 26, 2017; all enclosed pages cited. |
International Search Report and Written Opinion of corresponding application PCT/US2015/064634, dated Feb. 16, 2016, all enclosed pages cited. |
PCT/US2008/054190; Form PCT/ISA/237; Written Opinion; dated Jun. 30, 2008; all enclosed pages cited. |
PCT/US2008/054190; Form PCT/ISA/237; International Search Report; dated Jun. 30, 2008; all enclosed pages cited. |
Supplementary Partial European Search Report for corresponding European Application EP 08730070, dated May 15, 2015, all enclosed pages cited. |
Supplementary European Search Report for corresponding European Application EP 08730070, dated Oct. 5, 2015, all enclosed pages cited. |
Ernest M. Levin, Carl R. Robbins and Howard F. McMurdie, “Phase Diagrams for Ceramists”, Compiled at the National Bureau of Standards, Copyright 1964 by The American Ceramic Society, pp. 69 and 120, published in Columbus, Ohio. |
ASTM International Designation: C 347-57 (Reapproved 1983), “Standard Test Method for Reflectance, Reflectivity, and Coefficient of Scatter of White Porcelain Enamels”, copyright ASTM International International, Annual Book of Standards, vol. 14.02, published Dec. 1983, pp. 733-735. |
Herbert V. Oliveira et al., “Manual of Drying and Firing Porcelain Enamel”, PEI-601, Version 1.2, published by the Porcelain Enamel Institute, Nashville, Tennessee, copyright 1996-1997, pp. 1-22. |
Japanese Minister of International Trade and Industry and the Japanese Industrial Standards Committee, “Antimicrobial products-Test for antimicrobial activity and efficacy”, Standardiztion Journal translated and published by the Japanese Standards Association, Reference No. JIS Z 2801 : 2000(E), published Dec. 20, 2000, Tokyo, Japan, pp. 1-11. |
AATCC Committee RA31, “AATCC Test Method 100-1999, Antibacterial Finishes on Textile Materials: Assesment of”, AATCC Technical Manual/2003, pp. 149-151. |
Richard A. Eppler with Mimi Obstler, “Understanding Glazes”, published by The American Ceramic Society, Westerville, Ohio, 2005, pp. 246, 247, 315. |
ASTM International Designation: C286, “Standard Terminology Relating to Porcelain Enamel and Ceramic-Metal Systems”, copyright ASTM International 1999 (Reapproved 2009) published Jan. 2010, West Conhohocken, PA, pp. 1 and 4. |
The Edward Orton Jr. Ceramic Foundation, “Temperature Equivalent Chart for Orton Pyrometric Cones ( C)”, www.ortonceramic.com, 2011. |
Enamel; 9th Edition of Encyclopedia Britannica—free 9th Edition online Encyclopedia Britannica; vol. 8; all pages enclosed cited. |
United States Patent and Trademark Office; Translation of “Antibacterial Enamel And Its Preparation Method” by Wenzhan Ding; Chinese Patent Application No. 1843995; translated Dec. 2012; Phoenix Translations; Elgin, Texas; all enclosed pages cited. |
Office Action for corresponding Brazilian Patent Application No. PI0807590-5 dated Jan. 2, 2018, all enclosed pages cited. |
Number | Date | Country | |
---|---|---|---|
20180116226 A1 | May 2018 | US |