Dual hierarchical omniphobic and superomniphobic coatings
10253451 ยท 2019-04-09
Assignee
Inventors
Cpc classification
D06M23/08
TEXTILES; PAPER
C08L83/08
CHEMISTRY; METALLURGY
C09D5/00
CHEMISTRY; METALLURGY
D06M15/693
TEXTILES; PAPER
C09D183/08
CHEMISTRY; METALLURGY
C09D127/16
CHEMISTRY; METALLURGY
C09D127/16
CHEMISTRY; METALLURGY
C08L83/08
CHEMISTRY; METALLURGY
International classification
D06M23/08
TEXTILES; PAPER
C09D183/08
CHEMISTRY; METALLURGY
Abstract
The disclosed subject matter relates to an omniphobic material, including a substrate layer, a first layer of first nanoparticles, the first nanoparticles having a first size and including a particle core and a coating of a fluorodecyl POSS and fluoro-elastomer co-polymer and a second layer of second nanoparticles, the second nanoparticles having a second size and including a particle core and a coating of a fluorodecyl POSS and fluoro-elastomer co-polymer. The first layer of first nanoparticles contact the fabric layer and the second layer of second nanoparticles contact the layer of first nanoparticles. The second size of the second nanoparticles is larger than the first size of the second nanoparticles.
Claims
1. An omniphobic or superomniphobic material, comprising: a. a substrate layer including a fabric or a generally textured solid surface; b. a first layer of first nanoparticles, the first nanoparticles having a first size and including a particle core and a coating of a fluorodecyl POSS and fluoro-elastomer co-polymer; c. a second layer of second nanoparticles, the second nanoparticles having a second size and including a particle core and a coating of a fluorodecyl POSS and fluoro-elastomer co-polymer, wherein the first layer of first nanoparticles contact the substrate layer and the second layer of second nanoparticles contact the layer of first nanoparticles and the second size of the second nanoparticles is larger than the first size of the first nanoparticles.
2. The omniphobic material of claim 1, wherein each of the first nanoparticle core and the second nanoparticle core ranges in weight from about 0.0001 g to about 0.5 g.
3. The omniphobic material of claim 1, wherein the fabric is a tightly woven polyester fabric comprising at least one of 100% nylon, 50% nylon/50% cotton and 95% Nomex/Kevlar.
4. The omniphobic material of claim 1, wherein the amount of fluoro-elastomer ranges from about 15% of 1.0 g of the coating to about 60% of 1.0 g of the coating.
5. The omniphobic material of claim 1, wherein the amount of fluorodecyl POSS ranges from about 40% of 1.0 g of the coating to about 85% of 1.0 g of the coating.
6. The omniphobic material of claim 1, wherein the amount of fluoro-elastomer is about 50% of 1.0 g of the coating and the amount of fluorodecyl POSS is about 50% of 1.0 g of the coating.
7. The omniphobic material of claim 1, wherein the first size of first nanoparticles and the second size of second nanoparticles range in size from about 15 nm to about 3,000 nm.
8. The omniphobic material of claim 1, wherein the ratio of the second size of the second nanoparticles to the first size of the first nanoparticles is about 20:1.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) These and other features, aspects, and advantages of the present invention will become better understood when the following detailed description is read with reference to the accompanying drawings in which like characters represent like parts throughout the drawings, wherein:
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DETAILED DESCRIPTION
(8) There are three parameters that can be considered in developing an omniphobic or superomniphobic surface including (1) a surface with an apparent contact angle greater than 150 for a omniphobic surface and greater than 150 for a superomniphobic surface, (2) a micro/nano-roughness surface architecture and (3) local surface curvatures that are created by micro/nano-cavities in which liquid cannot wet the surface.
(9) The surface contact angle is illustrated
(10) The micro/nano-roughness surface architecture can be described using either of the two models.
(11)
(12) Local surface curvature is illustrated in the embodiment shown in
(13) Aspects of one embodiment are a durable, conformal omniphobic or superomniphobic coating including a very low surface tension cage-like molecule (for example, Fluoro-POSS, .sub.sv=10 mN/m) and a fluorinated elastomer (for example, Tecnoflon,
.sub.sv=12 mN/m). The resulting composition has very low interfacial energy between solid and vapor.
(14) Aspects of another embodiment include a fluorodecyl POSS (POSS being Polyhedral Oligomeric Silsesquioxane) (.sub.sv10 mN/m) and a fluoro-elastomer dissolved in a hydrochloro-fluorocarbon (HCFC) solvent. Upon curing, the solvent is evaporated and a co-polymer of the fluorodecyl POSS and fluoro-elastomer is formed.
(15) Aspects of another embodiment include a durable, conformal omniphobic coating that includes a very low surface tension cage-like molecule (Fluoro-POSS, 10 mN/m) and a fluorinated elastomer (Tecnoflon,
.sub.sv=12 mN/m). The very low surface tension cage-like molecule may have a
.sub.sv less than about 10 mN/m. The fluorinated elastomer may have a
.sub.sv less than about 12 mN/m.
.sub.sv corresponds to surface tension of the solid-vapor interface.
(16) Fluorodecyl POSS is a cage-like molecule as shown in the illustration in
(17) Suitable fluoro-elastomers can include Tecnoflon BR 9151 (.sub.sv12 mN/m) available from Solvay Solexis, Inc (.sub.sv12 mN/m) or a non-fluorinated elastomer such as silicone [i.e., polydimethylsiloxane (PDMS)] from various vendors. The .sub.sv for such fluoro-elastomers can range from about 12_mN/m to about 22.7 mN/m for fluoro-elastomers and from about 40 mN/m to about 70 mN/m for non-fluorinated elastomers.
(18) In the embodiments, the amount of fluorodecyl POSS may range from about 40% of 1.0 g to about 85% of 1.0 g and the amount of fluoro-elastomer may range from about 15% of 1.0 g to about 60% of 1.0 g. The preferred amounts are about 50% of 1.0 g of fluorodecyl POSS and about 50% of 1.0 g of fluoro-elastomer, the preferred fluoro-elastomer is Tecnoflon.
(19) The HCFC solvent can include Asahiklin AK225 (3,3-Dichloro-1,1,1,2,2-pentafluoropropane) solvent from Asahi Glass Company. Other suitable HCFC solvents that can be used include Vertrel XF from Chemours or Fluosov from Nugentec.
(20) Aspects of another embodiment include coating nanoparticles with a fluorodecyl POSS and a fluoro-elastomer in HCFC solvent and curing the composition to produce a fluorodecyl POSS and a fluoro-elastomer co-polymer coating with a nanoparticle suspension inside. The nanoparticles weight can range from about 0.0001 g to about 0.5 g, with the size ranging from about 10 nm to about 3,000 nm.
(21) Aspects of another embodiment include coating nanoparticles and coating a substrate, such as, for example, fabric or a generally textured solid surface (e.g., a roughened surface) with at least one layer of the so formed fluorodecyl POSS and fluoro-elastomer co-polymer coating with nanoparticle suspension or fluorodecyl POSS and fluoro-elastomer copolymer coated nanoparticles. This embodiment can include applying a plurality of layers of such co-polymer coating with suspended nanoparticles, including each layer having coated nanoparticles of substantially the same size and adjacent layers including coated nanoparticles of a substantially different size from layer to layer, preferably the size of the nanoparticles of successive layers are larger than the size of the previous layer. For example, for adjacent layers, the difference in size of the nanoparticles within the first layer and the subsequent second layer (second layer nanoparticle size: first layer nanoparticle size) can be about 20:1 (e.g., about 20 to 30 nm size particles in the first coating and about 500 nm size particles in the second coating; 500/[(20+30)/2]=20 to 1 ratio). Examples of nanoparticles include silicon oxide, titanium oxide, etc. which can be natural (i.e., non-treated), treated, charged, metalized, or magnetized.
(22) Aspects of a preferred embodiment is shown schematically in
(23) Aspects of another embodiment includes a method used to form the embodiments included herein. The method includes forming a first layer by immersing the fabric to be treated in a solution of fluorodecyl POSS and fluoro-elastomer in HCFC solvent that also includes the specific nanoparticles to be coated and applied to the fabric. The immersion process may take place from about 5 minutes to about 60_minutes. The coating time depends on the base fabric's composition since certain fabric may have to be surface treated to enhance coating/bonding effectiveness. The fabric can be laid flat to dry. Next, the coated fabric is cured for an amount of time ranging from about 30 minutes to about 1 hour at a temperature ranging from about 60 C. to about 65 C., preferably for about 12 hours at about 60 C. in, for example, a convection oven. The method includes forming a second layer by immersing the fabric to be treated in a different solution of fluorodecyl POSS and fluoro-elastomer in HCFC solvent that includes nanoparticles (preferably different in size, e.g., larger in size, from the nanoparticles used for the first layer) to be coated and applied to the fabric as a second layer. Similar immersion, laying flat and curing steps can again be followed for the second layer. Formation of inverse trapezoidal nano-features are formed through alignment of larger particles in the top layer (2.sup.nd coating) onto the smaller nanoparticles in the bottom layer (1.sup.st coating) using paramagnetic nano-particles.
(24) Successive coating and curing procedures lead to a durable, conformal super-nonwetting coated fabrics that would resist wetting by low surface tension liquids (including chemical warfare agents, toxic industrial chemicals) and have minimal attraction to dust and dirt. As a result, the fabric and clothing that it is made from are self-cleaning along with providing enhanced chemical/biological (CB) protection. For example, it provides a durable abrasion resistant super-nonwetting and dirt/dust resistant coating to textile products. When fabricated into clothing, the embodiments will provide the wearer (e.g., a warfighter) with textiles that will be extremely repellent to water, oil, and organic solvent, non-staining with minimal to no interference to air and evaporative cooling processes and may, for example, result in increased mission time in CB contaminated battlefield/environment as well as launderable/reusable clothing. The fabric embodiments also support civilian applications in self-cleaning clothing, all-weather gears, tent/shelters & textile structures, sport wears, etc.
(25) Successive coating of dual size nanoparticles embodiments forms inverse trapezoidal features on treated textile surfaces that exhibit extreme repellency to low surface tension nonpolar (e.g., Hexadecane, hexane) and polar (e.g., methanol) liquids, while allowing air and moisture vapor permeation, which is necessary for wear comfort.
(26) FluoroPOSS-Tecnoflon coating chemistry requires less changes in yarn size as compared to Fluoro-alkyl based polyurethane chemistry (UltraTech/Luna) to achieve the same liquid robustness. Therefore, FluoroPOSS-Tecnoflon provides advantages in fabric design in preventing liquid wet through resulting from dual size nano-particles and a reentrant structure that are also enhanced when used with a tightly woven fabric, for example, a tightly woven polyester fabric.
Examples 1-36
(27) Method: Applied double-layer coating, with 1.sup.st and 2.sup.nd layers containing nanoparticles. Solution used to apply coating to fabric: 100 mL of Asahiklin, 0.5 g of Fluoro-POSS, 0.5 g of Tecnoflon and nanoparticles Weight Range: 0.0001 g to 0.5 g, Size Range: 15-3,000 nm. Fabric: 100% polyester fabric. Application of each layer included dipping fabric into above Asahiklin, Fluoro-POSS, Tecnoflon and nanoparticles solution for 2 minutes in manually agitated solution; after removal coating fabric was laid flat to dry and cured for 12 hours at 60 C. in a convection oven. Asahiklin AK 225's Component: 3,3-Dichloro-1,1,1,2,2-pentafluoropropane (HCFC-225ca). CAS No. 422-56-0. 40-50%_Component: 1,3-Dichloro-1,1,2,2,3-pentafluoropropane (HCFC-225cb). CAS No. 507-55-1. 60-50%. Each sample was analyzed using apparent contact angle data of water, methanol, hexadecane, and hexane, and their SEM images. Examples 1-36 are identified as formulation numbers 23-58, respectively in the table shown in
(28) This written description uses examples as part of the disclosure, including the best mode, and also to enable any person skilled in the art to practice the disclosed implementations, including making and using any devices or systems and performing any incorporated methods. The patentable scope is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal languages of the claims.