Methods for fabricating transparent icephobic coatings, and transparent icephobic coatings obtained therefrom

Patent metadata

Field	Value
Publication number	US-11247228-B2
Application number	US-201816173255-A
Country	US
Kind code	B2
Filing date	Oct 29, 2018
Priority date	Aug 19, 2014
Publication date	Feb 15, 2022
Grant date	Feb 15, 2022

Abstract

Some variations provide a method of forming a transparent icephobic coating, comprising: obtaining a hardenable precursor comprising a first component and a plurality of inclusions containing a second component, wherein one of the first component or the second component is a low-surface-energy polymer, and the other is a hygroscopic material; applying mechanical shear and/or sonication to the hardenable precursor; disposing the hardenable precursor onto a substrate; and curing the hardenable precursor to form a transparent icephobic coating. The coating contains a hardened continuous matrix containing regions of the first component separated from regions of the second component on an average length scale of phase inhomogeneity from 10 nanometers to 10 microns, such as less than 1 micron, or less than 100 nanometers. The transparent icephobic coating may be characterized by a light transmittance of at least 50% at wavelengths from 400 nm to 800 nm, through a 100-micron coating.

First claim

What is claimed is:

1. A transparent icephobic coating comprising a first component and a plurality of inclusions containing a second component, wherein one of said first component or said second component is a low-surface-energy polymer selected from fluoropolymers having a surface energy between about 5 mJ/m 2 to about 50 mJ/m 2 , wherein the other of said first component or said second component is a hygroscopic material selected from polyesters or polyethers,
wherein said low-surface-energy polymer and said hygroscopic material are covalently connected in a segmented copolymer comprising:
(a) one or more first soft segments containing said fluoropolymers that are (α,ω)-hydroxyl-terminated and/or (α,ω)-amine-terminated;
(b) one or more second soft segments containing said polyesters or polyethers that are (α,ω)-hydroxyl-terminated and/or (α,ω)-amine-terminated;
(c) in one or more hard segments, a reacted form of one or more isocyanate species possessing an isocyanate functionality of 2 or greater; and
(d) in said one or more hard segments, a reacted form of one or more polyol or polyamine chain extenders or crosslinkers,
wherein said transparent icephobic coating has a glass-transition temperature higher than −80° C., and
wherein said first soft segments and said second soft segments are separated by an average length scale of phase inhomogeneity from about 0.2 microns to about 100 microns.

2. The transparent icephobic coating of claim 1 , wherein said fluoropolymers are present in said transparent icephobic coating at a concentration from about 15 wt % to about 35 wt %.

3. The transparent icephobic coating of claim 1 , wherein said fluoropolymers are selected from the group consisting of polyfluoroethers, perfluoropolyethers, and combinations thereof.

4. The transparent icephobic coating of claim 1 , wherein said polyester or polyether is a poly(ethylene glycol).

5. The transparent icephobic coating of claim , wherein said transparent icephobic coating is characterized by a light transmittance of at least 50%, at one or more wavelengths from 400 nm to 800 nm, through a 100-micron film of said transparent icephobic coating.

6. The transparent icephobic coating of claim 1 , wherein said transparent icephobic coating is characterized by a light transmittance of at least 80%, at one or more wavelengths from 400 nm to 800 nm, through a 100-micron film of said transparent icephobic coating.

7. The transparent icephobic coating of claim 1 , wherein said transparent icephobic coating is characterized by an AMIL Centrifuge Ice Adhesion Reduction Factor of about 50 or more when subjected to an AMIL Centrifuge Ice Adhesion Test.

Assignees

• Hrl Lab Llc

Inventors

• Rodriguez April R
• Nowak Andrew P
• Gross Adam F

Classifications

• C08G18/4833 Primary

  Polyethers containing oxyethylene units · CPC title

• B05D2401/31

  applied as mixtures of monomers and polymers · CPC title

• B05D2508/00

  Polyesters · CPC title

• C08G18/246

  containing also tin-carbon bonds · CPC title

• B05D1/06

  Applying particulate materials · CPC title