US2014314958A1PendingUtilityA1

Inorganic/organic hybrid nanolaminate barrier film

Assignee: AERIS CAPITAL SUSTAINABLE IP LTDPriority: Oct 31, 2003Filed: May 9, 2014Published: Oct 23, 2014
Est. expiryOct 31, 2023(expired)· nominal 20-yr term from priority
B05D 1/02B05D 3/0254B82Y 30/00B05D 1/005B05D 1/30B05D 7/56B05D 1/18Y10T428/139Y10T428/1359Y10T428/265Y10T428/1303Y10T428/2991B05D 5/083Y10T428/2998Y10T428/13Y10T428/1352H10K 50/8445
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Claims

Abstract

An inorganic/organic hybrid nanolaminate barrier film has a plurality of layers of an inorganic material that alternate with a plurality of layers of an organic material. Such a barrier film can be fabricated using nanocomposite self-assembly techniques based on sol-gel chemistry.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for making an inorganic/organic hybrid nanolaminate barrier film, comprising:
 combining an alkoxide, an alcohol, water dilute HCl and heating the resulting mixture. Introducing a coupling agent to the mixture,   introducing a surfactant to the mixture in a quantity sufficient that the initial surfactant concentration is below the critical micelle concentration;   adding to the mixture one or more polymer precursors suitable for the formation of a polymer selected from the group of, polyethylene naphthalate (PEN), polyether etherketone (PEEK), polyether sulfone (PES), fluorinated or non-fluorinated styrene polymer precursors, fluorinated or non-fluorinated methyl styrene polymer precursors, fluorinated or non-fluorinated (meth)acrylate polymer precursors, and combinations and/or derivatives of two or more of these precursors;   adding a cross-linker agent and an initiator to the mixture;   coating a substrate with the mixture; and   allowing the alcohol to evaporate so that the sol forms a film having alternating organic and inorganic layers.   
     
     
         2 . The method of  claim 1  further comprising incorporating one or more hydrophobic groups into the polymer precursors or eliminating one or more hydrophobic groups from the polymer precursors to increase and/or decrease the hydrophobicity of the organic layers. 
     
     
         3 . The method of  claim 2  wherein the one or more hydrophobic groups are selected from the group of non-polar hydrophobic groups, methyl groups, benzyl (aromatic) groups, PO 4   3− , SO 4   2− , CH 3 COOO − , Br − , NO − , ClO 4   − , I − , SC −  anions, NH 4   + , Rb + , K + , Na + , Cs + , Li + , Mg 2+ , Ca 2+ , Ba 2+  cations, tryptophan, isoleucine, phenylalanine, tyrosine, leucine, valine, methionine, alanine 
     
     
         4 . The method of  claim 3  wherein the surfactant includes one or more Gemini surfactants. 
     
     
         5 . The method of  claim 1  wherein the alkoxide includes tetraethylorthosilicate (Si(OCH 2 CH 3 ) 4  and the alcohol is ethanol. 
     
     
         6 . The method of  claim 5  wherein in molar ratios of the tetraethylorthosilicate, ethanol, water, and HCl are present in the mixture in molar ratios of 1:3.8:1:5×10 −5  respectively. 
     
     
         7 . The method of  claim 6 , wherein the coupling agent is 7-octenlytrimethoxysilane, or methacryloxypropyl trimethoxysilane. 
     
     
         8 . The method of  claim 7  wherein the surfactant is cetyltrimethylammonium bromide. 
     
     
         9 . The method of  claim 1  wherein the one or more polymer precursors include 2,6-Dimethylnaphthalene, or a set of monomers such as bisphenol A and di-para-fluorophenylsulfone. 
     
     
         10 . The method of  claim 1 , further comprising annealing the film at a temperature of about 125° to about 150° C. or greater and/or below the lowest decomposition temperature of any of the organic materials in the film. 
     
     
         11 . The method of  claim 1  wherein coating a substrate with the mixture includes depositing the mixture on the substrate by dip coating, spin coating, spray coating, web coating, or microgravure web coating.

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