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“All Epoxies Are Not The Same” Presented to Paint Applicator Division by Tony Ring. What is Epoxy?. The epoxide group, also termed as, oxirane or ethoxyline group, is a 3 member ring containing 2 carbons and an oxygen. Epoxy resin is defined as a molecule containing more than one epoxide group.
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“All Epoxies Are Not The Same”Presented toPaint Applicator Divisionby Tony Ring
What is Epoxy? The epoxide group, also termed as, oxirane or ethoxyline group, is a 3 member ring containing 2 carbons and an oxygen. Epoxy resin is defined as a molecule containing more than one epoxide group
Bis-A Epoxy • Most common epoxy resins are Diglycidyl Ethers produced from a reaction between Epichlorohydrin with Bisphenol A
Epoxy History • The first commercial attempts to prepare resins from epichlorohydrin occurred in 1927 in the United States. • Credit for the first synthesis of Bisphenol A based epoxy resins are shared by Dr. Pierre Castan of Switzerland and Dr. S.O. Greenlee in the United States in 1936. • Hexion, Dow and Huntsman are the largest producers of Epoxy Resins in the US with many foreign suppliers as well.
Other Epoxy Types • Other important glycidyl epoxies made from various alcohol containing compounds Phenolics: Mono-functional diluents, Bis-F and Novalac Resins Glycols: Poly-functional diluents and Flexibilizers Alcohols: Mono-functional diluents • Another class of epoxies is cycloaliphatic and aliphatic resins. These are non glycidyl epoxies that are formed by peroxidation of olefinic double bonds. They are used in UV cured formulations and outdoor applications. They are a minor segment of the market
Curing Agents • The epoxy group reacts with various molecules commonly know as curing agents to form highly cross linked thermoset polymers • Common curing agents are: Amines Polyamides Amidoamines Anhydrides Lewis Acids Organic Acids Phenols Thiols
Epoxy Reaction • A typical epoxy amine Reaction is outlined below: The remaining nitrogen protons continue to react to form the final ridge 3-D Network
Epoxy Properties Properties of optimally formulated cured epoxy systems • Low shrinkage • High shear and tensile strength • Will bond to a large verity of substrates • Low level of creep under sustained load • Good thermal resistance • Good electrical insulator • Chemical and solvent resistance • Stiffness • Good gap filling properties • Low or no VOCs present in formulations • Wide formulation latitude possible • Low cost to performance ratio
Property Modifications There are countless ways epoxy compound’s properties can be modified by adding various materials, such as: • Mineral fillers (ex. talc, silica, alumina, etc.) • Flexibilizers • Diluents (functional and external) • Pigments • Thickeners • Accelerators • Adhesion promoters • Impact modifiers • Tougheners
Property Modifications (cont) Modifications are made to: • Improve performance • Less rigid and brittle • Decrease cure time • Increased peel strength, etc. • Improve processing convenience • Reduce health hazards • Adjust mix ratios • Reduced cure times and temperature for one part systems • Reduce costs
Epoxy Applications Epoxy systems are widely used. Several applications areas are:
Formulating for Performance • Epoxy adhesives can be formulated to meet the performance requirements of almost any application • The key factor is to have the right epoxy for the application at hand • The formulator must understand the end use, application method and performance requirements. • With that knowledge, epoxies can be:
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