Bio-Based Epoxy Polymers, Blends, and Composites. Группа авторов
isosorbide (Figure 1.64) and it could be used for curing of diglycidyl ether of isosorbide giving the completely bio‐based epoxy system [150].
The diamine derivative of isosorbide is obtained using microwave assistant thiol‐ene coupling reaction in the aqueous media and with the water‐soluble initiator (NH4)2S2O8, as the alternative to AIBN. The cured isosorbide‐based resin has good shape fixity, good shape recovery, and satisfied thermal stability. This fully bio‐based resin shows great potential to be used as a candidate for shape memory material. Another synthetic method for obtaining the diamine derivative of isosorbide is the reaction of cyanoethylation of isosorbide, followed by the hydrogenation of di‐cyanoethylated product (Figure 1.65) [151].
Terpene derivatives might also be applied as bio‐based curing agents for epoxy resins. For example, a novel terpene‐based curing agent prepared as an adduct of myrcene, monoterpene containing three double bonds including conjugated diene, and maleic anhydride (MMY) is used to cure bisphenol A‐based epoxy resin [152]. The obtained cured material is characterized by a tensile strength of 48.74 MPa and a storage modulus of 19.06 MPa, but a poor impact property of 8.55 kJ/m2 and a very low elongation at break (7.54%). Improvement of properties of cured bio‐based epoxy resins is performed by application of mixture (mixed by weight ratios of 100/0, 75/25, 50/50, 25/75, and 0/100, respectively) of two curing agents: MMY and castor oil‐modified adduct of myrcene and maleic anhydride (CMMY) (Figure 1.66).
Figure 1.64 Synthesis of the isosorbide‐based cross‐linking agent.
Figure 1.65 Synthesis of the isosorbide‐based cross‐linking agent via cyanoethylation step.
Table 1.7 Properties of epoxy resin networks cured with bio‐based curing agents.
| Cured samples | Tg (°C) | E at Tg+30°C (MPa) | Tensile strength (MPa) | Elongation at break (%) | Impact strength (kJ/m2) |
|---|---|---|---|---|---|
| MMY100 | 61.59 | 19.06 | 48.74 | 7.5 | 8.55 |
| MMY75/CMMY25 | 58.03 | 19.00 | 42.11 | 6.5 | 13.87 |
| MMY50/CMMY50 | 54.03 | 4.18 | 35.55 | 6.6 | 17.29 |
| MMY25/CMMY75 | 45.09 | 2.72 | 11.11 | 259.4 | 62.51 |
| CMMY100 | 15.14 | 1.11 | 0.43 | 565.8 | Unbroken |
Based on the obtained results (Table 1.7), with the increase of CMMY weight ratio, the tensile strength and Tg of the cross‐linked resin decreases, but the elongation at break and the impact strength increase.
As can be seen from the examples presented above, it is possible to obtain not only epoxy resins from raw materials of natural origin but also cross‐linking agents for them. Interestingly, it is also possible to synthesize completely bio‐derived epoxy systems. Both the epoxy resins based on bisphenol A, as well as cross‐linked with curing agents on the basis of raw materials of natural origin, and the fully epoxy biosystems are characterized by very good final properties.
Figure 1.66 Synthesis of bio‐based epoxy curing agent derived from myrcene and castor oil.
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