Increasing demand for bio‐based epoxy thermoset alternatives has risen in the last few years. Epoxidized vegetable oils (EVO) have attracted significant attention due to their bio‐based, unharmful nature and high availability. This study proposes a fully bio‐based epoxy thermoset based on epoxidized linseed oil (ELO) and tannic acid (TA). TA allows, with its high degree of functionality and aromatic structure as a curing agent for ELO, to create a fully bio‐based polymer network with a high glass transition temperature (T_g), high stiffness, and high strength. A maximum T_g of 146 °C, a flexural modulus of 2986 MPa, and flexural strength of 72 MPa are obtained. The strong material properties of the TA/ELO thermoset expose its potential as a bio‐based substitute for petrochemical‐based epoxy resins for high‐performance applications.

In the present study, an epoxy compound, 1,2‐epoxy‐6‐methyl‐triglycidyl‐3,4,5‐cyclohexanetricarboxylate (EGCHC) synthesized from sorbic acid, maleic anhydride, and allyl alcohol is proposed. Using commodity chemicals, a bio‐based carbon content of 68.4 % for the EGCHC resin is achieved. When cured with amine hardeners, the high oxirane content of EGCHC forms stiff cross‐linked networks with strong mechanical and thermal properties. The characterization of the epoxy specimens showed that EGCHC can compete with conventional epoxy resins such as DGEBA. A maximum stiffness of 3965 MPa, tensile strength of 76 MPa, and T_g of 130 °C can be obtained by curing EGCHC with isophorone diamine (IPD). The cured resin showed to be decomposable under mild conditions due to the ester bonds. The solid material properties of EGCHC expose its potential as a promising bisphenol A, and epichlorohydrine free alternative to conventional petroleum‐based epoxies with an overall high bio‐based carbon content.

3-Carene is successfully utilized as renewable feedstock for the synthesis of biobased polyesters via ring-opening polymerization or polycondensation. These polyesters showed amorphous or semi-crystalline morphology, influencing thermal properties.

The salt-tolerant marine microalgae Dunaliella tertiolecta is reported to generate significant amounts of intracellular glycerol as an osmoprotectant under high salt conditions. This study highlights the phylogenetic distribution and comparative glycerol biosynthesis of seven new Dunaliella isolates compared to a D. tertiolecta reference strain. Phylogenetic analysis indicates that all Dunaliella isolates are newly discovered and do not relate to the D. tertiolecta reference. Several studies have identified light color and intensity and salt concentration alone as the most inducing factors impacting glycerol productivity. This study aims to optimize glycerol production by investigating these described factors singularly and in combination to improve the glycerol product titer. Glycerol production data indicate that cultivation with white light of an intensity between 500 and 2000 μmol m⁻² s⁻¹ as opposed to 100 μmol m⁻² s⁻¹ achieves higher biomass and thereby higher glycerol titers for all our tested Dunaliella strains. Moreover, applying higher light intensity in a cultivation of 1.5 M NaCl and an increase to 3 M NaCl resulted in hyperosmotic stress conditions, providing the highest glycerol titer. Under these optimal light intensity and salt conditions, the glycerol titer of D. tertiolecta could be doubled to 0.79 mg mL⁻¹ in comparison to 100 μmol m⁻² s⁻¹ and salt stress to 2 M NaCl, and was higher compared to singularly optimized conditions. Furthermore, under the same conditions, glycerol extracts from new Dunaliella isolates did provide up to 0.94 mg mL⁻¹. This highly pure algae-glycerol obtained under optimal production conditions can find widespread applications, e.g., in the pharmaceutical industry or the production of sustainable carbon fibers.