High Temperature Melt Integrity Battery Separators Via Spinning
US-2016348281-A1 · Dec 1, 2016 · US
US9260570B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9260570-B2 |
| Application number | US-201313860392-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 10, 2013 |
| Priority date | Apr 10, 2012 |
| Publication date | Feb 16, 2016 |
| Grant date | Feb 16, 2016 |
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In some embodiments, the present disclosure provides methods of strengthening liquid crystal elastomers. In some embodiments, such methods include a step of placing the liquid crystal elastomer in an environment that applies dynamic stress to the liquid crystal elastomer. In further embodiments, the methods of the present disclosure also include a step of providing liquid crystal elastomers for placement in an environment that applies dynamic stress. In some embodiments, the liquid crystal elastomer is in a nematic phase before or during the application of dynamic stress. In some embodiments, the application of dynamic stress enhances the stiffness of the liquid crystal elastomer by more than about 10%. Further embodiments of the present disclosure pertain to liquid crystal elastomers that are made by the methods of the present disclosure.
Opening claim text (preview).
What is claimed is: 1. A liquid crystal elastomer with enhanced stiffness, wherein the liquid crystal elastomer comprises a mobile nematic director capable of rotating or re-orienting in response to dynamic stress, and a mesogen associated with a polymer, wherein the stiffness of the liquid crystal elastomer is enhanced by placing the liquid crystal elastomer in an environment that applies dynamic stress to the liquid crystal elastomer, wherein the liquid crystal elastomer is in a nematic phase before or during the application of dynamic stress, and wherein the application of dynamic stress enhances the stiffness of the liquid crystal elastomer by more than about 10%. 2. The liquid crystal elastomer of claim 1 , wherein the dynamic stress is applied by dynamic compression. 3. The liquid crystal elastomer of claim 1 , wherein the dynamic stress is applied below the nematic to isotropic transition temperature (T NI ) of the liquid crystal elastomer. 4. The liquid crystal elastomer of claim 1 , wherein the liquid crystal elastomer is a polydomain liquid crystal elastomer. 5. The liquid crystal elastomer of claim 1 , wherein the liquid crystal elastomer has a mesogen content ranging from about 20% molar content to about 90% molar content of the liquid crystal elastomer. 6. The liquid crystal elastomer of claim 1 , wherein the mesogen is selected from the group consisting of aromatic rings, aliphatic rings, poly aromatic rings, poly aliphatic rings, phenyls, biphenyls, benzenes, and combinations thereof. 7. The liquid crystal elastomer of claim 1 , wherein the mesogen is functionalized with one or more functional groups, wherein the functional groups are selected from the group consisting of alkenes, alkanes, alkynes, carboxyl groups, esters, halogens, and combinations thereof. 8. The liquid crystal elastomer of claim 1 , wherein the polymer is selected from the group consisting of polysiloxanes, poly(methyl)siloxanes (PMS), poly(dimethyl)siloxanes (PDMS), poly(hydrogen methyl)siloxanes (PHMS), and combinations thereof. 9. The liquid crystal elastomer of claim 1 , wherein the mesogen is cross-linked to the polymer. 10. The liquid crystal elastomer of claim 1 , wherein the application of dynamic stress enhances the stiffness of the liquid crystal elastomer by between about 10% to about 90%.
Liquid crystals · CPC title
with mesogenic groups in the side chain · CPC title
After-treatment of articles without altering their shape; Apparatus therefor (B29C44/56, B29C73/00 take precedence; surface shaping B29C59/00 {; for joined or sealed parts B29C66/03; after-treatment specially adapted for vulcanising tyres B29D30/0633}) · CPC title
Polysiloxanes · CPC title
containing boron or metal atoms · CPC title
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