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Epoxy Cure Chemistry Part 5: Putting it all together

March 31, 2014 By Jeffrey Gotro 1 Comment

Thermoset network schematicIn the series on epoxy cure chemistry we covered epoxies, curing agents, and the chemical crosslinking pathways (nucleophilic reactions).  In this post we will discuss how to put all the pieces together to do some “molecular engineering” to formulate products with different fully cured properties.  This type of approach has been used extensively in commercial products from adhesives, to laminates to structural composites.

Let’s recall that epoxies are supplied in a wide range of molecular weights (n can vary in the chemical structure below) and amine curing agents also can have various molecular weights as well as seen in the figure showing the various types of Jeffamine (1) curing agents.

diglycidyl ether of bisphenol AJeffamine epoxy curing agents

 

 

 

 

Let’s look at a few different molecular architectures.  In the following examples we assume that the epoxy functionality is two and the amine functionality is four (remember primary amines can react with two epoxy groups).

The first case is where the molecular weights between the crosslinks is higher at approximately 1000 (for example EPON 1001F or DER 671 see references 2 and 3))

High molecular weight epoxy between crosslinks

In this case the final cured network will have LOWER

Glass transition temperature (Tg)
Modulus
End use temperatures

but have HIGHER

Toughness
Flexibility

 

In the second case the molecular weight between crosslinks is smaller at approximately 380 (for example EPON 828 or DER 331, see references 2 and 3))

Low molecular weight epoxy between crosslinks

In this case the final cured network will have HIGHER

Glass transition temperature (Tg)
Modulus
End use temperatures
Solvent resistance

but have LOWER

Fracture toughness
Flexibility (more brittle)

In the above two examples, we kept the amine constant and showed the effect of changing the epoxy chain length between crosslinks.  One could envision even more customization by using longer or shorter amine curing agents such as the Jeffamine series above.  For example, using a long chain epoxy (EPON 1007F, MW is approximately 2900) and a long chain diamine (Jeffamine D-2000, MW is approximately 2000) would lead to a very low Tg network that is tough and highly elastic.

In structural composite applications, the goal is to have high Tg, high modulus and stiffness, good resistance to chemicals, and high end use temperatures.  A common epoxy formulation used a four functional epoxy and an aromatic diamine.

The figure below shows the chemical structure of 4,4′-diaminodiphenylmethane (TGDDM) such as MY 720 and MY 721 from Huntsman:

Tetra functional epoxy TGDDM

and 4,4′-diaminodiphenylsulfone(DDS):

4 4 DDS

Due to the highly aromatic structures and the functionality of each molecule is four, then a very tightly crosslinked, high modulus network will result.  One drawback of the highly crosslinked network is low fracture toughness, but there are many ways to improve the fracture toughness.

References:

1) Jeffamines are trademarks for amine curing agents provided by Huntsman Performance Products.  Click for detailed product information

2) Momentive Performance Materials. click for more details

3) Dow Chemical. click for more details

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« Epoxy Cure Chemistry Part 4: Nucleophiles in Action
Characterization of Thermosets »

Comments

  1. Paul Berger says

    October 25, 2015 at 10:03 AM

    Very informative. How can I reach you for a further discussion

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Polymer Innovation Blog

I’m Dr. Jeff Gotro and welcome to the Polymer Innovation Blog. Over the last 40 years I have been involved in polymer research, along with product and process development. I acquired invaluable experience working for IBM, AlliedSignal, Honeywell, Ablestik Labs (now Henkel) and in multiple consulting projects. In this blog, I (along with some guest contributors) will share our experiences, tips, and “tricks of the trade” to get more out of your innovation efforts and discuss new trends and technical advances in the polymer industry.
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