Epoxy resins carry strained, three-membered epoxide rings that open and crosslink with amine hardeners. The result is unmatched adhesion and chemical resistance for primers, floors, linings and composites.
Functional groupEpoxide (oxirane) ring
Found inPrimers · Floors · Linings
Key specEEW
04Part A
Ep
Epoxy Resins
8 compounds profiled
Overview
Adhesion and chemical resistance, built in
Most coating epoxies are glycidyl ethers: molecules made by reacting a bisphenol or phenolic resin with epichlorohydrin so that each end carries an epoxide ring. The standard liquid resin is based on bisphenol A; bisphenol F versions are thinner and more solvent-resistant; novolac epoxies carry more rings per molecule for maximum chemical and heat resistance.
When mixed with an amine hardener, each active hydrogen opens one ring and the network grows in three dimensions. The aromatic backbone and dense crosslinks give epoxies their hallmark adhesion to steel and concrete, hardness, and resistance to water, fuels and many chemicals.
That same aromatic structure absorbs UV, so standard epoxies chalk and amber outdoors. They usually serve as primers and intermediate coats, topcoated with polyurethane or polyaspartic where appearance matters. Reactive diluents thin resins for self-leveling floors, at some cost to chemical resistance.
Key compounds
Resins and reactive diluents
The base resins and modifiers behind epoxy primers, floors and linings.
BPA epoxyAromaticLiquid
Bisphenol A liquid epoxy resin (DGEBA type)
CAS
Type
BPA–epichlorohydrin resin
EEW
~182–192
Used forGeneral-purpose floors, primers, tank linings and composites.
The workhorse standard liquid epoxy. Excellent adhesion, but chalks and ambers in sunlight.
The epoxide ring is a strained triangle of two carbons and one oxygen. An amine nitrogen attacks the less hindered carbon, the ring springs open and a hydroxyl group is left behind. A primary amine has two hydrogens, so it can open two rings, and the hydroxyls formed along the way help adhesion.
Getting the ratio right matters more than with most chemistries. Using EEW for the resin and AHEW for the hardener, parts of hardener per 100 parts resin = AHEW × 100 ÷ EEW. Off-ratio mixes leave unreacted material that softens the film and reduces chemical resistance.
Epoxy cure depends strongly on temperature. Below roughly 10 °C (50 °F) many systems slow dramatically, and humid air promotes amine blush on the surface.
Epoxide ring + amine
Part AGlycidyl ether resin
+
Part BR′–NH₂Amine hardener
Ring opens, network grows
R–CH(OH)–CH₂–NH–R′β-Hydroxy amine
phr hardener = AHEW × 100 ÷ EEW
Compare
Epoxy resin types compared
Generalized ratings (5 = best). Hardener choice and formulation shift these considerably.
Resin
Typical EEW
Viscosity
Chemical resistance
UV resistance
Typical use
Bisphenol A
182–192
Medium
Floors, primers, linings
Bisphenol F
165–175
Low
Self-leveling floors, linings
Epoxy novolac
172–181
High
Tank linings, containment
Hydrogenated BPA
210–240
Low
Weatherable topcoats
With reactive diluent
Varies
Very low
Thin, flowable floor systems
Epoxy safety essentials
Uncured epoxy resins and amine hardeners are among the most common causes of occupational allergic contact dermatitis. Sensitization builds with repeated skin contact.
Never let resin or hardener touch bare skin: wear nitrile gloves and long sleeves
Wear eye protection, since hardeners can cause serious eye damage
Ventilate, especially with reactive diluents and solvent-borne epoxies
Mix only what you can use: large masses can overheat and smoke
Leave mixed leftovers to cure in a safe, open area before disposal
Clean skin with soap and water, never with solvents
Always follow the product’s Safety Data Sheet, your employer’s safety program and local regulations. This page is general reference information, not a substitute for them.
FAQ
Common questions
What is EEW?
Epoxide equivalent weight: the grams of resin that contain one epoxide group. Standard liquid bisphenol A resin is about 182–192 g/eq. It is used with the hardener’s AHEW to calculate the mix ratio.
Why do epoxies yellow or chalk outdoors?
The aromatic bisphenol structure absorbs UV light, which breaks down the surface. Outdoor epoxies are usually topcoated with a UV-stable polyurethane or polyaspartic.
Bisphenol A or bisphenol F epoxy?
BPF resins have lower viscosity, better solvent resistance and less tendency to crystallize in cold storage. BPA resins are the economical, general-purpose standard. Many floor systems blend both.
What is a reactive diluent?
A low-viscosity glycidyl ether, such as C12–C14 alkyl glycidyl ether, that thins the resin and reacts into the network. It improves flow but lowers crosslink density and chemical resistance.