Manufacturers of high-performance paint & coating formulations, as well as related applications like adhesives, inks, and sealants, incorporate organofunctional silanes to achieve key performance enhancements. To support the formulator in these applications, Gantrade offers an array of silanes applicable to both water-based and solvent-based systems. Organofunctional silanes complement Gantrade’s position in acrylic monomers, vinyl acetate monomer, and diacetone acrylamide (DAAM) & adipic acid dihydrazide (ADH). DAAM & ADH constitute a crosslinking technology called “keto-hydrazide crosslinking.” This technology also imparts important improvements in paint & coatings formulations
The primary function of organofunctional silanes in paint & coatings are:
Interfacial adhesion promoters
Coupling a polymer matrix to mineral fillers and pigments
Crosslinking of the polymer matrix to enhance performance
Key improvements achievable with organofunctional silanes in paint & coating formulations include the following:
Greatly enhanced wet and dry adhesion
Scratch, scrub, and abrasion resistance
Water, blister, chemical, cleaner, and corrosion resistance
Improved pigment and filler dispersion and higher loadings
Surface blocking resistance
Rheological properties, including higher flow and reduced viscosity
A longer service life is an overall product benefit for paint & coating formulations enhanced by organofunctional silanes.
The Chemistry of Organofunctional Silanes
Paint & coatings formulators most often use bifunctional silanes to improve adhesion to coated surfaces, bridge the interface between dissimilar materials, and to effect crosslinking. Built around one central silicone atom, organofunctional silanes work through two complementary modes of functionality:
Non-hydrolyzable organofunctional or vinyl moieties on the Si atom that either copolymerize or react with other functionality on organic polymeric materials (e.g. epoxides, carboxylic acids or amines) to build durable covalent bonds.
Hydrolyzable silane moieties, as in silyl esters, form a reactive silanol group which condenses with surface hydroxyl groups on pigments, fillers, surfaces, or other siloxane moieties to form siloxane -Si-O-Si- linkages. Through drying, they create multiple chemical bonds that form strong attachments to inorganic surfaces.
Z – a functional group like an amine, epoxy or (meth)acrylate, etc. that forms chemical bonds with organic materials including monomers and polymers
X – three moisture hydrolyzable groups, typically an alkoxy (methoxy or ethoxy), which hydrolyze to form chemical bonds with inorganic materials such as glass, minerals, etc.
Hydrolysis of the alkoxy-silanes occurs in waterborne systems or can result from sources of adventitious water, such as moisture in an integral mixture, surface water, added water, or absorption from the atmosphere. Under acidic conditions, hydrolysis is significantly faster than under basic conditions. Except for amino-silane systems, users deploy most silanes under acidic conditions. A pH of near 7 is preferred for storage stability. The rate of methoxy silyl esters hydrolysis is about six to ten times faster than the rate of hydrolysis of ethoxy silyl esters. Note also that methoxy-silanes hydrolyze to produce methanol, while ethoxy silanes release ethanol, a more toxicologically acceptable side-product.
The silyl esters portion of the molecule couple with active hydroxyl moieties on the surfaces of inorganic materials and/or generate crosslinks through the formation of siloxane -Si-O-Si- linkages Silica, talc, clay, and metal surfaces such as steel are examples of inorganic materials with effective concentrations of active hydroxyl surface functionality. Silanes not only enhance bond strengths, but they also prevent debonding at a surface or interface, for example under moist conditions.
Gantrade’s Silane Product Slate for Paints & Coatings
Depending on the polymer and resin system to be silane modified, the synthesis chemist and formulator have many different modes of incorporating silane functionality into a paint and coating formulation. Synthetic chemists most often select methacryloxypropyl trimethoxysilane, GC-Si 174 in acrylic systems, whereas they most often choose to copolymerize vinyltrimethoxysilane, GC-Si 171 in vinyl systems. Polymer chemists accomplish this goal by adding these dual functional silanes to the monomer feed mix during copolymerization.
They also accomplish silane modification under neutral and ambient conditions by post addition of an aminosilane in an acrylic emulsion, solvent based formulation or epoxy based protective coating. Manufacturers often use diamino-silanes in emulsion systems, because they show better water solubility. Another functionality to consider is the ureidosilane. Glycidyloxy (epoxy) silanes are an alternative for the chemical modification of acrylic systems having functionality that reacts with the epoxy silane (see the Polymer Selection Guide at the end of this paper). Polymer chemists can graft epoxy silanes onto polymers that contain a functional group, such as carboxylic acid salts, ammonium, or volatile amine salts or an amine group. They can catalyze the reaction by organo-titanate or organo-tin catalysts. Also they can add a second component to affect the reaction of the epoxy silane with a functional polymer–adipic dihydrazide (ADH), for example. We recommend epoxy silanes in epoxy and phenolic-based protective coatings.
When crosslinking silane modified polymers and resins, premature crosslinking must not occur prior to application, in order to avoid interference with the coalescence process in an emulsion system and to ensure the siloxane portion of the molecule is available for bonding, filler coupling, and surface adhesion. Crosslinking prior to coalescence in an emulsion creates weak boundaries between the emulsion particles and a reduction in the film strength with the concomitant reduction in abrasion, scrub and scratch resistance. Gel formation and viscosity build can occur with premature crosslinking.
Manufacturers use organofunctional silanes directly, usually in a volatile solvent, as surface treatments or primers, or pre-compounded with fillers. We recommend amino silanes and glycidyloxy silanes in this case. Users may accomplish pre-hydrolysis of the silyl ester with added water or surface moisture. After surface drying for 15-30 minutes, users can apply protective coatings to the surfaces.
Generally, the starting organofunctional silane dose level is 0.2 – 1.0 %, unless high loadings of fillers are involved, in which case the silane loading can be up to 2 %. Manufacturers can achieve remarkable improvements with low level additions of these bifunctional silanes, especially under humid or wet conditions. We recommend testing to find the optimum level of silane; achieving too high of a silane level can cause a reduction in properties.