Finals: All In Flashcards
Why is it necessary for resins to have high shear strength?
If shear stress is applied to the composite, the matrix will be displaced at a different rate than the fibers because of the properties of these components. High shear strength will lead to a more uniform displacement
Why does a matrix need low creep?
to prevent the deformation of the material under long term stress and to be able to keep the fibers in place as well
Why is it important for matrixes to have the same CTE as the fiber?
If these two have different CTE, they will expand at different rates and apply load or forces onto one another. When this happens, stresses will develop between their interface, which is detrimental to the mechanical properties of the composite, and this may also cause delamination and debonding of the fiber.
Why do you want the matrices to have low moisture absorption?
So that water molecules don’t adhere to the surface and interior during processing, which may reduce interaction and contact between the fiber and matrix, so their bond strength may not as be as strong as it could be.
Why do you want the matrix to have a low viscosity during processing?
A low viscosity will lead to more contact time between the fiber and matrix, which increases the chances of good matrix and fiber wetting, which therefore leads to better interaction between the components. High viscosity will have shorter contact time and less wet-out
What is fiber wet out?
It is the full impregnation and surface coating of the fibers with the resin, which is what allows the fiber and the matrix to bond and interact
Why do you need good flow characteristics during processing for the matrix?
Good flow characteristics will lead to the mold filling fully, corners are reached, and it won’t take to long or too short of a time
Why is rapid curing and solidification of matrix important?
Because curing is the step which takes the most amount of time
Why would one want the curing temperature of the matrix to not greatly be above the product usage temperature?
So that more energy is not required/wasted or expended for curing
How come it’s important for shrinkage to be low during and after molding?
This leads to better dimensional stability. Shrinkage entails poor dimensional stability, which may make the composite unsuitable for the application. Also, if only the matrix shrinks and not the fiber, they will push against each other, which leads to stresses, poor bonding, and delamination/debonding.
Why is the shelf life of thermosets more limited compared to thermoplastics?
There is potential for thermoset matrices to crosslink during storage
Why to thermosets have a tendency to shrink more than thermoplastics?
For thermosets, due to the cross-linking and structure, there is going to be the formation of bonds due to the presence of leading groups. When these are formed, there is going to be bond alignment, and this alignment/arrangement allows the composite to be more compressed (i.e. shrinkage).
What are the two thermoplastic resins we learned about and the four thermoset resins?
TP: PEEK and Polyimide
TS: PF Resin, Polyester, Vinylester, Epoxy
For composites, what is the component that dictates composite processing? Why?
The matrix, because fibers are the ones that tend to be more stable and more easily processible.
In processing, why is it important to account for the viscosity of the matrix, what does it dictate?
- fiber-wet out (due to contact time)
- flow time and flow pattern
True or false, curing time is often what dictates the overall process cycle time. Why?
True, because it is the longest step in composite processing. So it naturally takes the most time, and is like the “rate-limiting” step.
In the processing of thermosets, why are fabricators or manufacturers given only incompletely polymerized pre-polymers (stage-B polymers) in the semi-liquid/solid form, and the ones who convert the polymer to its C-stage?
Stage B polymers are more fusible and can be handled to be brought to the desired shape, however, they are not too rigid to the point that they can’t flow (Stage C).
What are the two types of PF resins, and what are their main differences?
- Novolac - manufactured with less formaldehyde (less OH groups), and they have an acid catalyzed reaction
- Resole - manufactured with excess formaldehyde (more OH groups), and these have a base-catalyzed reaction
For PF resins, formaldehyde exists in what form typically?
Formalin
Resole is known to have an excess of formaldehyde and therefore more OH groups. What does this entail and why is this relevant for the final product?
OH groups are crosslinking sites, and more crosslinking entails more bond formation (and leaving groups) and therefore more bond alignment. This bond alignment will lead to a greater amount of shrinkage for the product, making it dimensionally unstable for its application.
Novolac has less OH groups compared to Resole because it was manufactured without an excess of formaldehyde. What is the advantage of this?
To drive the crosslinking reaction, usually more formalin is added. This means that you can control WHEN crosslinking occurs and the DEGREE to which the resin will crosslink, based on when you add formalin or how much you add.
What are the main advantages of PF resin?
cheap, thermally/dimensionally stable, and there’s generally good chemical, mechanical, and electrical properties
What are the main disadvantages of PF resin?
Think of OH groups:
1. leaving groups -> many byproducts -> water -> evaporation -> voids
2. high shrinkage
3. high water absorption
4. easily attacked by aqueous bases
Where are PF resins most used?
“Bakelites” or Laminates for high voltage insulators (i.e. plugs, switches, etc.)
What are polyester resins made from, and how does this influence the polyester?
Dibasic acids and diols. Combination of these due to the difference in their structures impart variation in mechanical properties like flexural strength, tensile strength, and compressive strength.
What is the main drawback of the polyster resin due to its structure containing ester bonds?
It is very prone to hydrolysis and isn’t environmentally stable because of the ester bonds.
Why do polyester resins have the ability to gel together, and what can be done to slow this down?
The free ends of chains are reactive, and therefore can interact to form longer chain networks, which leads to gel formation. To slow this down, inhibitors can be added.
What are some of the main applications of polyester matrices?
- dinghies/workboats
- chairs
- sportscar bondies
What are the pros of polyester as a matrix?
- cheap
- rigid
- easy to handle/shap
What are the cons of polyester as a matrix?
- easy gelling and crosslinking
- prone to hydrolysis
- short shelf-life
- only moderate mechanical properties
- high cure shrinkage
For vinyl esters, what is this usually comprised of?
Styrene monomer (in PE solution)
Styrene as a monomer minimizes gelation and viscosity for vinyl esters. How?
Since styrene is now surrounding the polyester chains, the free ends can no longer interact, and so there’s no more attachment between the chains.