Carbon-based solid acid catalysts were prepared using rice straw (RS) waste, and the effects of carbonization temperature and sulfonation temperature on the catalytic activity were investigated. The properties of the catalysts were characterized using thermo gravimetric (TG), scanning electron microscope (SEM), Brunauer–Emmet–Teller (BET), Fourier transform infrared spectroscopy (FT-IR), temperature-programmed desorption (TPD), and X-ray photoelectron spectroscopy (XPS), and their activities were investigated through the hydration of α-pinene. The conversion of α-pinene and the selectivity of α-terpineol reached 67.60% and 57.07% at 80 °C and atmospheric pressure in 24 h, respectively. The high catalytic capacity of the catalyst is attributed to the high acid site density and high porosity of the catalyst. TPD analysis and FT-IR spectroscopy showed that the catalyst produced by low-temperature carbonization at 300 °C followed by low-temperature sulfonation at 80 °C had abundant strong acid sites (0.82 mmol/g), which can effectively inhibit the side reactions of hydrated α-pinene. The total acidity reached 2.87 mmol/g. N₂-physisorption analysis clearly indicated that the obtained catalysts were mesopore-predominant materials, and the S_BET and V_Total of catalysts reached 420.9 m²/g and 4.048 cm³/g, respectively. Preparation of the catalyst involves low energy consumption, and its cheap raw materials make the whole process simple, economical, and environmentally friendly.

In the treatment of joints, mucosa, and full-thickness wounds, traditional implant surgery presents not only inconvenience but also a significant risk of wound infection. Additionally, the pharmaceutical application of mangiferin (MGF) has been severely restricted due to its poor water solubility. In this study, we report the synthesis and characterization of sodium-mangiferin (MGF-Na(S)) using the salt formation method. This novel compound exhibits a solubility of up to 80 mg ml⁻¹, which is remarkably 800 times higher than that of MGF. Subsequently, MGF-Na(S) was combined with water to synthesize an injectable sodium-mangiferin homopolymeric hydrogel (MGF-Na(HG)). The hydrogel was further characterized, and its wound-healing properties were investigated. The results indicate that MGF-Na(HG) effectively extends the residence time of therapeutic agents on the wound surface, thereby enhancing wound healing. Moreover, this hydrogel forms a protective gel layer that prevents exogenous bacterial reinfection, providing an optimal environment for wound healing. Furthermore, the hydrogel demonstrated excellent self-healing and injectable properties, highlighting its potential for managing postoperative wounds. The successful utilization of this injectable, self-healing, and antibacterial MGF-Na(HG) in wound healing offers a novel approach for the application of MGF.