Chinese herbal medicine has offered an enormous source for developing novel bio-soft materials. In this research, the natural polysaccharide isolated from the Chinese herbal medicine Dendrobium was employed as the secondary building block to fabricate a “hybrid” hydrogel with synthetic poly (vinyl alcohol) (PVA) polymers. Thanks to the presence of mannose units that contain cis-diol motifs on the chain of the Dendrobium polysaccharides, efficient crosslinking with the borax is allowed and reversible covalent borate ester bonds are formed. Eventually, highly dynamic and double-networked hydrogels were successfully prepared by the integration of Dendrobium polysaccharides and PVA. Interestingly, the introduction of polysaccharides has given rise to more robust and dynamic hydrogel networks, leading to enhanced thermal stability, mechanical strength, and tensile capacity (>1000%) as well as the rapid self-healing ability (<5 s) of the “hybrid” hydrogels compared with the PVA/borax single networked hydrogel. Moreover, the polysaccharides/PVA double network hydrogel showed selective antibacterial activity towards S. aureus. The reported polysaccharides/PVA double networked hydrogel would provide a scaffold to hybridize bioactive natural polysaccharides and synthetic polymers for developing robust but dynamic multiple networked hydrogels that are tailorable for biomedical applications.

Ensuring long-term wellbore integrity is critical for carbon dioxide geological storage. Ordinary Portland cement (PC) is usually used for wellbore primary cementing and plug operation, and set cement is easily corroded by acidic fluids, such as carbon dioxide, in underground high-temperature and high-pressure (HTHP) environments, resulting in a decrease in the mechanical properties and an increase in permeability. In order to achieve long-term wellbore integrity in a CO₂-rich environment This study introduces materials such as thermosetting vinyl ester resin (TSR), filler composite resin (FCR), and low-cost resin cement (RC). Corrosion experiments were conducted using four materials in 28 days under supercritical carbon dioxide gas and water phase conditions of 60 °C and 10 MPa. The samples were characterized through mechanical property testing machines, core permeability measuring instruments, FTIR, XRD, and SEM. The results proved that after corrosion, PC mechanical properties decreased, the permeability increased, and the microscopic composition and morphology changed greatly. Penetrating corrosion occurs in the sample in the gas phase environment, and propulsive corrosion from outside to inside occurs in the water phase environment. However, TSR, FCR, and RC materials all maintain excellent resistance to carbon dioxide corrosion in gas and water environments. They have higher compressive strength and extremely low permeability compared to ordinary Portland cement. These three materials’ compressive strengths can be maintained around 131, 99, and 58 MPa, and permeability can be stabilized at <6 × 10⁻⁷, <6 × 10⁻⁷, and 0.16 mD levels. In summary, the above three materials all show better performance than ordinary Portland cement and are promising alternative materials that can be used in primary cementing and plug operations of carbon dioxide geological storage wells.