DETECTING ANTIMICROBIAL SURFACES

Abstract

A method includes depositing an antimicrobial material onto a surface of a substrate. The method includes binding a photochromic material to the antimicrobial material. Depositing the antimicrobial material and binding the photochromic material can include forming a mixture of the antimicrobial material and the photochromic material and depositing the mixture onto the surface of the substrate. It is also contemplated that depositing the antimicrobial material and binding the photochromic material can include first depositing the antimicrobial material onto the surface of the substrate and then depositing the photochromic material onto the antimicrobial material.

Claims

1. A method comprising: depositing an antimicrobial material onto a surface of a substrate; and binding a photochromic material to the antimicrobial material.

2. The method as recited in claim 1, wherein depositing the antimicrobial material and binding the photochromic material includes: forming a mixture of the antimicrobial material and the photochromic material; and depositing the mixture onto the surface of the substrate.

3. The method as recited in claim 1, wherein depositing the antimicrobial material and binding the photochromic material includes: first depositing the antimicrobial material onto the surface of the substrate; and depositing the photochromic material onto the antimicrobial material.

4. The method as recited in claim 1, wherein the antimicrobial material includes Si-QAC (3-(trimethoxysilyl) Propyldimethyl Octadecyl Ammonium Chloride).

5. The method as recited in claim 1, wherein the photochromic material includes at least one of sulfonates, sulfates, carboxylates, acrylates, phosphates, and/or phosphonates.

6. The method as recited in claim 1, wherein the antimicrobial material includes Si-QAC and the photochromic material includes anionic moiety, wherein binding the photochromic material to the antimicrobial material includes the anionic moiety binding to ammonium in the Si-QAC.

7. The method as recited in claim 6, wherein the anionic moiety binding to ammonium in the Si-QAC includes the sulfonates binding to a quaternary ammonium in respective spiked molecules of the Si-QAC.

8. The method as recited in claim 1, wherein the photochromic material is an anionic dye with absorbance near-UV which undergoes isomerization to become visible under near-UV illumination and remain invisible absent the near-UV illumination.

9. The method as recited in claim 1, further comprising: illuminating the photochromic material to reveal if any of the antimicrobial material is compromised or missing.

10. The method as recited in claim 9, further comprising if any of the antimicrobial material is revealed by illumination to be compromised or missing: re-applying the antimicrobial material and re-applying the photochromic material.

11. An antimicrobial structure comprising: a substrate; an array of spiked molecules of antimicrobial material extending from a surface of the substrate; and photochromic material bound to the spiked molecules.

12. The structure as recited in claim 11, wherein the substrate includes at least one of: an aircraft seat surface, an aircraft tray table surface, an aircraft magazine pouch surface, an aircraft seat handle surface, an aircraft luggage bin surface, an aircraft overhead bin surface, an aircraft lavatory surface, an aircraft galley surface, and/or an aircraft cockpit surface.

13. The structure as recited in claim 11, wherein the antimicrobial material includes Si-QAC (3-(trimethoxysilyl) Propyldimethyl Octadecyl Ammonium Chloride).

14. The structures as recited in claim 11, wherein the photochromic material is an anionic dye with absorbance near-UV which undergoes isomerization to become visible under near-UV illumination and remain invisible absent the near-UV illumination.

15. An antimicrobial material comprising: a mixture of an antimicrobial material and a photochromic material.

16. An antimicrobial surface comprising: a substrate; a coating comprising an antimicrobial material deposited on the substrate; a photochromic material bound on at least a portion of the antimicrobial substrate.

17. The antimicrobial surface as recited in claim 16, wherein the photochromic material is deposited as an array.

18. The antimicrobial surface as recited in claim 16, wherein the photochromic material is bound on only a portion of the antimicrobial material.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0012] So that those skilled in the art to which the subject disclosure appertains will readily understand how to make and use the devices and methods of the subject disclosure without undue experimentation, preferred embodiments thereof will be described in detail herein below with reference to certain figures, wherein:

[0013] FIG. 1 is a schematic view of an embodiment of an antimicrobial structure constructed in accordance with the present disclosure, showing the spiked molecules of the antimicrobial material and the photochromic material bound to the spiked molecules;

[0014] FIG. 2 is a schematic view of an example of the antimicrobial structure of FIG. 1, showing the molecular bond between one of the spiked molecules and the photochromic material;

[0015] FIG. 3 is a schematic view of a method in accordance with the subject disclosure, showing a procedure for monitoring and maintaining the antimicrobial structure; and

[0016] FIG. 4 is a schematic perspective view of the structure of FIG. 1, showing photochromic material deposited on the antimicrobial material in a pattern or array.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0017] Reference will now be made to the drawings wherein like reference numerals identify similar structural features or aspects of the subject disclosure. For purposes of explanation and illustration, and not limitation, a partial view of an embodiment of an antimicrobial structure in accordance with the disclosure is shown in FIG. 1 and is designated generally by reference character 100. Other embodiments of systems in accordance with the disclosure, or aspects thereof, are provided in FIGS. 2-4, as will be described. The systems and methods described herein can be used to provide antimicrobial surfaces that can be checked using an illuminator to confirm presence/efficacy of the antimicrobial surface.

[0018] The antimicrobial structure 100 includes a substrate 102. An array of spiked molecules 104 of antimicrobial material 105 extend from a surface 106 of the substrate 102. Photochromic material 108 may be bound to at least a fraction of the spiked molecules 104. The substrate 102 can include at least one of an aircraft seat surface, an aircraft tray table surface, an aircraft magazine pouch surface, an aircraft seat handle surface, an aircraft luggage bin surface, an aircraft overhead bin surface, an aircraft lavatory surface, an aircraft galley surface, and/or an aircraft cockpit surface, or any other suitable surface. The photochromic material 108 need be bound on only a portion of the antimicrobial material 105 on the substrate 102, as shown in FIG. 4. The photochromic material 108 can be deposited as an array or pattern such as the pattern shown in FIG. 4 or any other suitable pattern including a decorative pattern.

[0019] As shown in FIG. 2, the antimicrobial material can include Si-QAC (3-(trimethoxysilyl) Propyldimethyl Octadecyl Ammonium Chloride). With respect to the photochromic material 108, it can be a dye with an anionic moiety. The anionic moiety allows the dye molecules to ionically bond to the cationic ammonium, e.g., the quaternary ammonium, portion of the antimicrobial spiked molecules 104. The photochromic material 108 can include spiropyrans (as shown in FIG. 2), indolino-naphthoxazines, diarylethenes, naphthopyrans, and/or spirooxazines. Examples of suitable anionic moieties for the antimicrobial material 108 include sulfonates, sulfates, carboxylates, acrylates, phosphates, phosphonates.

[0020] The photochromic material 108 is an anionic dye with absorbance near-UV which undergoes isomerization to become visible under near-UV illumination and remain invisible absent the near-UV illumination. The photochromic dye reacts differently than a fluorescent dye. Fluorescent dyes react by exciting an electron via light (typically UV), and the resulting falling electron emits light. In fluorescent dyes there is no structural change to the molecule. In a photochromic compound, the illumination actually results in temporary bond breaking (photoisomerism), and that breakage results in emitted light. The effect is illumination such as near-UV illumination can make the dye appear to have a visible color it does not have in the absence of the near-UV illumination. For aesthetics the surface 106 thus appears to be whatever color is desired unless the illumination is present. The antimicrobial function of the combined photochromic, antimicrobial material is not impacted by the bonding of the photochromic material 108 to the spiked molecules 104.

[0021] With reference now to FIG. 3, a method 200 includes depositing 202 an antimicrobial material onto a surface of a substrate, e.g. substrate 102 of FIG. 1. The method includes binding a photochromic material, e.g. photochromic material 108 of FIG. 1, to the antimicrobial material. The antimicrobial material can be formed into a mixture of the antimicrobial material and the photochromic material and the method can include depositing the antimicrobial, photochromic mixture onto the surface of the substrate. It is also contemplated that the antimicrobial material can be deposited onto the substrate first, and then the photochromic material can be deposited onto the antimicrobial material.

[0022] The method 200 can include illuminating 204 the photochromic material to reveal if any of the antimicrobial material is compromised or missing. For example, on an aircraft a crew member can shine a near-UV flashlight on surfaces to check the antimicrobial coatings. The photochromic color will show under illumination if the antimicrobial material is intact on a given surface. If any of the antimicrobial material is revealed by illumination to be compromised or missing, the method can include re-applying the antimicrobial material and re-applying the photochromic material. The checking by illumination and reapplication as needed can be repeated on a regular basis, as indicated by the decision box 204.

[0023] This disclosure provides for inspection at manufacture, coating quality, coverage, highly sensitive inspection of coating, which can be invisible when not under irradiation, and can optionally be premixed into a coating solution prior to application, potentially reducing additional labor. Simple inspection is possible under an illuminator, which can provide confidence about the efficacy of the antimicrobial function. The materials can be turned for specific colors/wavelengths for aesthetics.

[0024] The methods and systems of the present disclosure, as described above and shown in the drawings, provide for antimicrobial surfaces that can be checked using an illuminator to confirm presence/efficacy of the antimicrobial surface. While the apparatus and methods of the subject disclosure have been shown and described with reference to preferred embodiments, those skilled in the art will readily appreciate that changes and/or modifications may be made thereto without departing from the scope of the subject disclosure.