Fast coating compositions

Abstract

An anticorrosive coating includes a first curable liquid layer to the associated substrate, the first layer having a thickness of at least about 100 micrometers, wherein the first layer includes at least one polymer or at least one monomer, quasi-one-dimensional particles or quasi-two-dimensional particles, sacrificial metal particles, and a solvent, wherein a percolation threshold of the particles is not reached in the presence of the solvent, wherein the percolation threshold of the particles is reached when between about 1% and about 20% of the solvent evaporates, applying a second curable liquid layer having a thickness of at least 100 micrometers on the top of the first layer after the percolation threshold of the particles is reached and viscosity of the first layer increases more than 50%, and allowing the first layer and the second layer to cure simultaneously.

1 . A self-stratifying anticorrosive coating comprising:
 a zinc-rich epoxy;   a curing agent chosen from the group consisting of amines, thiols, phenols, and carboxylic anhydrides;   a binding agent chosen from the group consisting of aminoalkyl dialkoxysilane, dimethoxysilane, and aminoalkyl trialkoxysilane;   a graphitic material;   a solvent; and   a water scavenger.   
     
     
         2 . A self-stratifying anticorrosive coating comprising:
 sacrificial metal particles;   graphitic material;   a first monomer;   at least a second monomer or at least a first polymer; and   a material that prevents the polymerization of at least one monomer inside the coating.   
     
     
         3 . The coating of  claim 2  further comprising:
 a curing agent; and 
 a binding agent. 
 
     
     
         4 . The coating of  claim 3 , wherein the first monomer and the at least a second monomer or at least a first polymer are chosen from the group consisting of epoxies, polyurethane, acrylates, methacrylates, vinyl ethers, cycloaliphatic epoxides, oxetanes, epoxides, photopolymers, siloxanes, and polyurea. 
     
     
         5 . The coating of  claim 4 , wherein the graphitic material is chosen from the group consisting of single walled carbon nanotubes, double walled carbon nanotubes, multiwalled carbon nanotubes, single sheet graphene, double sheet graphene, or multi-sheet graphene. 
     
     
         6 . The coating of  claim 5 , wherein the material that prevents the polymerization of at least one monomer inside the coating is a water scavenger chosen from the group consisting of liquid water scavengers, molecular sieves, silica, metal salts, and metal oxides. 
     
     
         7 . The coating of  claim 2 , wherein the sacrificial metal particles are chosen from the group consisting of any metal that has more positive redox potential then iron. 
     
     
         8 . The coating of  claim 7 , wherein the sacrificial metal particles are chosen from the group consisting of zinc, magnesium, aluminum, and alloys thereof. 
     
     
         9 . The coating of  claim 2 , wherein the curing agent is chosen from the group consisting of amines, thiols, phenols, and carboxylic anhydrides, and the binding agent is chosen from the group consisting of silanes with at least two alkyl groups. 
     
     
         10 . The coating of  claim 2 , wherein the coating further comprises a photoinitiator chosen from the group consisting of 1-hydroxy-cyclohexyl-phenyl-ketone, 2-hydroxy-1-[4-(2-hydroxyethoxy)phenyl]-2-methyl-1-propanone, 2,2-dimethoxy-2-phenylacetophenone, Bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide, triphenyl sulfonium triflate, triaryl sulfonium hexafluoroantimonate salts, triaryl sulfonium hexafluorophosphate salts, bis(eta 5-2,4-cyclopentadien-1-yl)-bis(2,6-difluoro-3-(1H-pyrrol-1-yl)-phenyl)titanium, 5,7-diiodo-3-butoxy-6-fluorone, 2,4,5,7-tetraiodo-3-hydroxy-6-fluorone, and 2,4,5,7-tetraiodo-3-hydroxy-9-cyano-6-fluorone. 
     
     
         11 . A method for a self-stratifying anticorrosive coating on an associated substrate comprising the steps of:
 mixing together a monomer or a polymer, a solvent, a graphitic material, and sacrificial metal particles;   adding a material that prevents polymerization inside the coating before, and immediately after, application on the associated substrate; and   adding a silane mixture.   
     
     
         12 . The method of  claim 11  further comprising the steps of:
 adding a curing agent; and 
 applying, in one spraying, the mixture of the monomer or polymer, the solvent, the graphitic material, and the sacrificial metal particles, the silane mixture, and the curing agent to the associated substrate, wherein an external effector hydrolyzes the silane mixture creating silicic acid, wherein the silicic acid spontaneously polymerizes into siloxane. 
 
     
     
         13 . The method of  claim 11 , wherein no insulating layer is used. 
     
     
         14 . The method of  claim 13  wherein the external effector is ambient moisture or photons. 
     
     
         15 . The method of  claim 11 , wherein the monomer or polymer is chosen from the group consisting of epoxies, acrylates, methacrylates, vinyl ethers, cycloaliphatic epoxides, oxetanes, epoxides, photopolymers, siloxanes, and polyurea. 
     
     
         16 . The method of  claim 11 , wherein the graphitic material is chosen from the group consisting of single walled carbon nanotubes, double walled carbon nanotubes, multiwalled carbon nanotubes, single sheet graphene, double sheet graphene, or multi-sheet graphene. 
     
     
         17 . The method of  claim 16 , wherein the material that prevents the polymerization inside the coating is a water scavenger chosen from the group consisting of liquid water scavengers, molecular sieves, silica, metal salts, and metal oxides. 
     
     
         18 . The method of  claim 17 , wherein the sacrificial metal particles are chosen from the group consisting of any metal that has more positive redox potential then iron. 
     
     
         19 . The method of  claim 18 , wherein the sacrificial metal particles are chosen from the group consisting of zinc, magnesium, aluminum, and alloys thereof. 
     
     
         20 . The method of  claim 11 , wherein the coating further comprises a photoinitiator chosen from the group consisting of 1-hydroxy-cyclohexyl-phenyl-ketone, 2-hydroxy-1-[4-(2-hydroxyethoxy)phenyl]-2-methyl-1-propanone, 2,2-dimethoxy-2-phenylacetophenone, Bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide, triphenyl sulfonium triflate, triaryl sulfonium hexafluoroantimonate salts, triaryl sulfonium hexafluorophosphate salts, bis(eta 5-2,4-cyclopentadien-1-yl)-bis(2,6-difluoro-3-(1H-pyrrol-1-yl)-phenyl)titanium, 5,7-diiodo-3-butoxy-6-fluorone, 2,4,5,7-tetraiodo-3-hydroxy-6-fluorone, and 2,4,5,7-tetraiodo-3-hydroxy-9-cyano-6-fluorone, wherein the curing agent is chosen from the group consisting of amines, thiols, phenols, and carboxylic anhydrides, and the binding agent is chosen from the group consisting of aminoalkyl dialkoxysilane, dimethoxysilane, and aminoalkyl trialkoxysilane.