Chemistry of Ambient Cure Epoxy Resins and Hardeners (2024)

Chemistry of Ambient Cure Epoxy Resins and Hardeners (1)A common ambient cure two-component paint chemistry involves the reaction of anepoxy resin with that of an amine functional resin (hardener). Due to their tenacious adhesion and moisture resistance, crosslinked epoxy resins are used on a variety of surfaces including metals and concrete, epoxy two-component compositions are used in a variety of applications including primers for exterior and interior applications.

Reactivity of epoxy groups with amine hardeners

As Table II illustrates, epoxy groups react with primary amines at ambient temperatures to form secondary amines that can in turn react to form tertiary amines. In terms of reaction rate of various epoxy and amines, Table I lists a few general structural-reactivity relationships of epoxy groups with amines hardeners.

Table I – General comparison of the reactivity rate of functional groups in epoxy and amine hardeners

Amine reactivity Primary > Secondary > Tertiary
Amine reactivity Reaction rate increases with increasing base strength
Amine reactivity Decreases with an increase in steric hindrance
Amine reactivity Aliphatic > aromatic or cycloaliphatic
Epoxy reactivity Aromatic (for example a bisphenol A based epoxy) > Aliphatic (ie. hydrogenated version of Bisphenol A based epoxy)
Epoxy reactivityTerminal epoxy groups > internal epoxy groups

Table II – Example of reactions of epoxy with amine

Chemistry of Ambient Cure Epoxy Resins and Hardeners (2)

With the correct catalyst,aliphatic epoxyresins can react with carboxyl functionality even at room temperature. Cycloaliphatic epoxy-based systems (ie. Using hydrogenated BPA as a building block) also provide improved light stability for exterior applications.

When formulating a stoichiometric reaction, it is desirable to discuss reactants in terms of equivalents.

Calculating mix ratios of epoxy – polyamine

For example, to calculate the stoichiometric parts by weight of hardener per 100 parts per hundred weight of epoxy resin:

phr = Amine Hardener Eq. Wt. X 100 / Epoxy Eq. Wt. of resin

For example, if the epoxy resin Eq. Wt. = 400 and the amine hardener Eq. Wt. is 100

The phr = 10000/400 = 25.0

Accordingly, 25.0 parts of amine curing agent are needed to cure 100 parts of epoxy resin for a 1:1 stoichiometric ratio of amine hardener: epoxy resin.

Epoxy resins

Per the diagram below, most epoxy resins are made by reacting Bisphenol A (BPA) with an excess of epichlorohydrin so the end groups are glycidyl ethers. The molecular weight and the epoxy equivalent weight are controlled by the ratio of epichlorohydrin EPC:BPA. Bisphenol F (BPF) based epoxy resins are more flexible than that of BPA-based epoxies. Hydrogenated BPA based epoxy resins provide improved exterior weathering as the aromatic groups that absorb UV are absent. Other epoxy resin types include epoxy-novolac (EN) and epoxy-phenolic (EP). Epoxy-novolac (EN) resins provide a higher crosslink density as they have a higher functionality (epoxy functional side chains) and thus provide a higher crosslink density and better chemical resistance. Epoxy-phenolics are also known for their chemical resistance coupled with excellent corrosion resistance.

Chemistry of Ambient Cure Epoxy Resins and Hardeners (3)

Chemistry of Ambient Cure Epoxy Resins and Hardeners (4)

Other hardeners

In addition to amine functional hardeners for use in curing of epoxy-functional resins, polyamides, amidoamines, phenalkamines and mercaptan functional curing agents provide improved low temperature cure rates. For example, polymercaptans cure with epoxies at 0 C to – 20 C. Solvent selection is another important factor in formulating epoxy-amine two component systems. Suitable hydrogen acceptor solvents such as t-butyl acetate can prolong pot life. Most ketones and esters (except for TBA) should be avoided since they form ketimines especially with primary amines at room temperature and this results in a reduction in the amount of active amine. Alcohols also slowly react with epoxy groups at room temperature. If mono-alcohols are used there is little change in viscosity. However, over time, this decreases the number of epoxy functional groups present and results in a reduction of the crosslink density of Part A containing epoxy resin and a primary alcohol solvent.

Accelerators

Tertiary amines act like cure accelerators, along with water, some alcohols, and some weak acids such as phenols. For example, 2,4,6-[Tris(dimethylaminomethyl)] phenol has both phenolic and tertiary amine groups and is also an effective catalyst. Weak acids promote the ring opening reaction of the epoxy.

The UL Prospector search engine provides a number of amine hardeners and epoxy resins for formulating two-component and other types of epoxy coatings.

Further Reading and Sources:

  • Prospector Knowledge Center:
    • Reactive silanes for Enhancement of Coating Performance
    • Chemistry of Resins and Hardeners
  • Organic Coatings, Science and Technology, Third and Fourth editions
  • Wikipedia

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Chemistry of Ambient Cure Epoxy Resins and Hardeners (5)

Ronald J. Lewarchik, President and CEO of Chemical Dynamics, LLC, brings 40 years of paint and coatings industry expertise to his role as a contributing author with the Prospector Knowledge Center. As a contributing writer, Ron pens articles on topics relevant to formulators in the coatings industry. He also serves as a consultant for the Prospector materials search engine, advising on issues related to optimization and organization materials within the database.

Ron’s company, Chemical Dynamics, LLC (www.chemicaldynamics.net), is a full-service paint and coatings firm specializing in consulting and product development based in Plymouth, Michigan. Since 2004, he has provided consulting, product development, contract research, feasibility studies, failure mode analysis and more for a wide range of clients, as well as their suppliers, customers and coaters.

He has also served as an Adjunct Research Professor at the Coatings Research Institute of Eastern Michigan University. As such, Ron was awarded a sub-grant from the Department of Energy to develop energy-saving coating technology for architectural applications, as well as grants from private industry to develop low energy cure, low VOC compliant coatings. He taught courses on color and application of automotive top coats, cathodic electro-coat and surface treatment. His experience includes coatings for automotive, coil, architectural, industrial and product finishing.

Previously, Ron was the Vice President of Industrial Research and Technology, as well as the Global Director of Coil Coating Technology for BASF (Morton International). During his fourteen-year tenure with the company, he developed innovative coil coating commercial products primarily for roofing, residential, commercial and industrial building, as well as industrial and automotive applications. He was awarded fifteen patents for new resin and coating formulas.

From 1974 to 1990, Ron held positions with Desoto, Inc. and PPG Industries. He was the winner of two R&D awards for coatings utilizing PVDF resins, developed the first commercial high solids automotive topcoat and was awarded 39 U.S. patents for a variety of novel technologies he developed. He holds a Masters in Physical Organic Chemistry from the University of Pittsburgh and subsequently studied Polymer Science at Carnegie Mellon University.

Ron lives in Brighton, Michigan with his family. Contact Ron via emailor through his company’s web site at www.chemicaldynamics.net to learn more about his consulting services…

Chemistry of Ambient Cure Epoxy Resins and Hardeners (2024)
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