Thermoset Plastics

1. Thermoset Plastics • Polymerization by chemical reaction of two or more monomer resins often at high temperature, with catalysts or mixing • Product is insoluble, often intractable • Generally not reversible • Product manufacturing by forming shape during reaction • Examples and applications: • Polyurethanes: Sport boots, convey belt, coatings • Phenolic: Billiard balls, car distributor caps • Epoxy: paint, adhesives, composites • Unaturated polyesters • Vinyl esters • Bismaleimides • Melamines

3. Mix • Two piece liquids - Vast bulk of mixture formed by the bulk resin), with catalyst. Mixing carried out by the user. Cure Initiated Bulk polymer + catalyst Crosslinked Solid Catalysed Liquid Thermoset resins are processed in various physical forms. High performance resins have very high viscosity, or may be actually solid at room temperature. No solvent- eliminates waste & shrinkage

4. One piece liquids - All components pre-mixed by the manufacturer. Cure is initiated by increased temperature, pressure, or exposure to UV light. Cure Initiated w/ elevated Temp Pre-mixed Catalysed Liquid Crosslinked Solid

5. Cure Initiated w/ elevated Temp Add Heat Crosslinked Solid Pre-mixed Catalysed Solid Pre-mixed Catalysed Liquid All components pre-mixed by manufacturer, and the solution remains solid at room temperature. Heat is applied to raise the resin above melting temperature. Further heat and pressure are applied to initiate cure. • One pieceSolids - TYPICAL OF THERMOSET PREPREGS

6. Common examples of thermoset polymers include glues, paints, and other surface coatings. We will consider laminating resins, those commonly used as composite matrices. As compared to TP’s, TS’s are brittle at room temperature, andcannot be reshaped due to the strong cross-linking covalent bonds. However, their comparative advantages include; • Higher tensile strength and stiffness • Excellent chemical and solvent resistance • Good dimensional and thermal stability • Good creep resistance • Excellent fatigue properties • Low viscosities, simplifying physical processing

7. Thermosets Liquid Monomer(s), Oligomeric Precursors, Thermoplastic with curable groups Elastomer Chemical reaction Glassy Thermoset or Vulcanized Elastomer Molding: Complex shapes-vulcanizing elastomers Reaction Injection Molding: RIM: Mixing two monomers or precursors

8. -Point at which covalent bonds begin to connect between linear chains, forming regions of large networks. Gelation: Two of the most important transitions are gelation and vitrification; -The resin transforms from a liquid to a rubbery state. -The reaction continues at a significant rate. -There is a drastic increase in viscosity.

9. Crosslinked networks Catalysed solution Gel: A two-phase structure. Vitrification: -Occurs when the glass transition temperature of the curing resin increases to the current resin temperature. at Gelation: Liquid -The rate of the cure reaction is significantly reduced, as further crosslinking requires diffusion of molecules through the network. -The final physical phase depends on the temperature the process has been held at.

10. Gel Point 0 1 Time (Degree of cure) For some manufacturing processes, it is important to consider viscosity of the resin as the cure reaction progresses. During the early stages of cure, the pre-polymeric chains are combining, and the average molecular weight of the mixture increasing. The viscosity therefore increases. Initially the increase will be relatively slow, significantly quickening as the “gel point” is reached.

12. The influence of temperature and time is best appreciated through consultation of the Time-Temperature-Transformation (TTT) diagram . Kind of like a phase diagram for metals… remember.. . Phase Transformations – (Gel and Vitrification) Thermoset resins may assume various physical forms, or phases during the cure reaction, depending on the temperature history. TTT diagram Depicts: • Important temperatures • Transitions between states Note: log time scale!

13. Tg is the glass transitiontemperature of the fully crosslinked polymer. TgGEL is the temperature at above which gelation occurs before vitrification. Tg0 is the glass transition temperature of the unreacted components. Below Tg0the catalysed solution will be a glassy solid. The crosslinking reaction can only occur very slowly, by diffusion (months or years). Thermosets used in prepregs are stored below Tg0 .

14. Between Tg0andTgGEL, the catalysed solution is in a liquid state. Crosslinking occurs until vitrification, where a transition to a glassy solid is made. The reaction is very slow thereafter. Between TgGEL andTg, the liquid catalysed solution gels first, ending the possibility for flow. Crosslinking continues at a good rate until vitrification. Above Tg, the liquid catalysed solution gels, but will never vitrify. The polymer remains in a rubbery state throughout the curing process. Once temperature is brought below Tg , vitrification occurs.

15. The full cure line on the TTT diagram denotes when the cross-linking operation is completed . Some parts are post-cured at a higher temperature, for a significant time, to ensure full cure, and the best properties (long times though) . At vitrification the resin will not necessarily be 100% cured. Some amount of the unreacted components remain, and the reaction will continue very slowly from this point. Full Cure

16. Not only are these reactions exothermic, but their reaction rates are also affected strongly by the local temperature of the resin. Tair Tair Consider the “slab” of thermoset resin curing below: T(z) Tair Tair The Thermoset Cure Reaction Thermoset cure reactions are highly exothermic, generating significant heat during the crosslinking process. This heat must be removed from the part.

17. Semi-crystalline thermoplastic Tm Td HDT Tg Hard, stiff Leathery Degraded Liquid (Tm) Td HDT Tg Thermoset Hard, stiff Semi-rigid Degraded, Char Temperature

18. E Highly Crosslinked Lightly Crosslinked Tg Temperature Solid Thermoset Properties Due to crosslinking between polymer chains, thermosets are typically stiffer, but more brittle than thermoplastics. Their resulting stiffness is a function ofthe degree of crosslinking, and the application temperature. While a crosslinked thermoset will not melt, degradation of the polymer will occur above a certain temperature.

19. Epoxy resin is made from the2-part kits. It’s the basis of composites like fiberglass, carbon fiber composites etc. Apart from an excellent glue, it is an important molding compound for rapid prototyping. Tensile strength 60 MPa Stiffness 2.6 GPa Chemical and corrosion resistant Low shrinkage Cures with amines, alcohols (higher temp) and carboxylic acids (higher still) Epoxies

20. Epoxy Curing Chemistry Epoxy pre-polymer Epoxy Linear Cured Epoxy catalyst

21. Insoluble Epoxies: Branched Polyamines

22. Epoxies

23. Polyester Thermosets (TS) or Unsaturated Polyesters (UP) • Largest group of thermosets • Most like to be reinforced with fiberglass “Casting Resin”

24. Unsaturated Polysters

25. Vinyl Esters (VE) Intermediate between polyesters & epoxies in performance and cost

26. Vinyl Esters (VE)

27. Formaldehyde Resins • Phenolic • Urea formaldehyde • Melamine formaldehyde

28. Phenol-Formaldehyde Resins Residual formaldehyde in cross-linked matrix

29. Phenol-Formaldehyde Resins Novolacs are widely used photoresists Both of these are reactive thermosets

30. Thermoset Types • Phenolics

31. Polymeric Foams • Polymers can be combined with a gas • Forms voids or cells in the polymer • causing the polymer to be very light • Referred to as cellular, blown, • expanded polymer, foam • Elastomeric foam- matrix (polymer) is an elastomer or rubber • Flexible foam- soft plastic matrix, e.g., plasticized PVC (PPVC), LDPE, PU • Rigid foams- PS, unsaturated polyesters, phenolics, urethanes (PU) • Type of polymer matrix, thermoplastic or thermoset can form basis for classification • Amount of gas added reflects the resulting density • Light foams: density = 0.01 to 0.10 g/cc (1 to 6 lb/ft3) • Dense foams: density = 0.4 to 0.6 g/cc (25 to 40 lb/ft3) • Note: water = 1g/cc or 62.3 lb/ft3 Photomicrograph (10X) of cross-section of rigid phenol-formaldehyde

32. Mechanisms for the formation of cellular structure • Aeration or frothing: mechanical agitation is used to incorporate air into liquid resin system (latex, reactive urethane) • Physical blowing agent: • Add N2 gas into solution or to liquid melt which comes out of solution when pressure is released and forms cells. • Add liquids at room temperature and have low boiling point. The liquids vaporize upon heating or by chemical reaction heat. • Aliphatic hydrocarbons (pentane), methylene chloride, trichloro-fluoromethane, or freon 11

33. Polystyrene: PS or expanded polystyrene foam (EPS) • Made from expandable polystyrene beads which are small spheres of polystyrene (diameter of 0.3 – 2.3 mm) containing 3-7% pentane as physical blowing agent • Bulk density of beads (with air spaces) is 0.7 g/cc. • Manufacturing • Beads are pre-expanded with the use of a steam chamber to a bulk density of 0.02-0.05 g/cc. • Beads are cooled and reached equilibrium with air penetrating the cells. • Placed back in steam chamber and molded into final foamed shape. • Forms basic cellular structure is closed cell type • Large blocks are molded which are cut into insulating boards or molded into custom products • Cups, insulating containers, protective elements • Extrusion process can be used with blowing agent • Meat trays, egg cartons

34. Chemical Blowing Agents • Compounds that decompose under heat and liberate large amounts of and inert gas, • N2, CO2, CO, water, ammonia, H2, etc. • Activators can sometimes be added to allow lower decomposition temperature and release more gas at a lower temperature. • Early blowing agents were • Sodium bicarbonate, which liberates CO2 • Other carbonates and nitrates liberate hydrogen or nitrogen. • Hydrogen can be generated in large quantities, but diffuses away quickly • Organic compounds can be used for some high temperature thermoplastics • Toluene sulfonyl hydrazine • azodicarbonamide • Toluene sulfonyl semicarbazide • Phenyl tetrazole • Can be in finely divided solid form to create cellular structure • Nucleating agents and surfactants are used to control cellular structure

35. Melamines

36. Polybismaleimides Printed wiring boards, carbon fiber composites for aerospace Brittle but can be toughed with chain extension using Michael addition chemistry

37. Polybismaleimides Mp 155 °C Tg > 500 °C Tensile Strength 41-83 MPa Tensile Modulus 4-5 GPa

38. Polyimides: Thermoplastic Thermoset-like High operating temperatures (up to 500 °C) High tensile strength & modulus Low creep and outgassing Flame resistant Solvent resistant Composites, high temperature adhesives, wire insulation for extreme environments

40. Polyimides:Kapton Operating temperature range: -269 °C to 400 °C Composites, space suits, dielectric material for printed wiring boards Poor resistance to mechanical wear: wiring in aircraft shorted out due to Kapton failure Kapton( DuPont)

41. Polyimide Thermosets

42. Polyurethanes Soft or thermoplastic elastomers

43. More Flexible Polyurethanes

44. Polyurethanes

45. Polyurethane or Polyurea Thermosets Rigid-high moldulus

46. Polyurethane Foams Soft foam Solvent blown foam

47. Polyurethane Foams Soft foam

48. Green Polyurethane Foams

49. A variety of solid properties are relevant to manufacturing; 1.0 – 6.5 1100-1230 3.1 – 4.6 50 – 75 3.0 – 8.0 1120-1130 3.1 – 3.3 70 – 81 1.5 – 8.0 1100-1200 2.6 – 3.8 60 – 85 1.8 1000-1250 3.0 – 4.0 60 – 80 400-450 1200 0.7 30 – 40 1.5 – 3.3 1200-1320 3.2 – 5.0 48 – 110 1.5 – 3.0 1430-1890 3.1 – 4.9 100 – 110 2800 72 >540 7790 205 640 Tensile Strength s MPa Strain to Failure e % Density r kg/m3 Young’s Mod E GPa Polyester Vinylester Epoxy Phenolic PUR BMI PI Aerospace Al Carbon Steel ** Last two materials provided for reference * At room temperature

50. Common Shaping Processes for Thermosets