In this study, an injectable thermoresponsive hydroxypropyl guar-graft-poly(N-vinylcaprolactam) (HPG-g-PNVCL) copolymer was synthesized by graft polymerization. The reaction parameters such as temperature, time, monomer, and initiator concentrations were varied. In addition, the HPG-g-PNVCL copolymer was modified with nano-hydroxyapatite (n-HA) by in situ covalent cross-linking using divinyl sulfone (DVS) cross-linker to obtain HPG-g-PNVCL/n-HA/DVS composite material. Grafted copolymer and composite materials were characterized using Fourier transform infrared spectroscopy, thermogravimetric analysis, proton nuclear magnetic resonance spectroscopy (¹H NMR), and differential scanning calorimetry. The morphology of the grafted copolymer (HPG-g-PNVCL) and the composite (HPG-g-PNVCL/n-HA/DVS) was examined using scanning electron microscopy (SEM), which showed interconnected porous honeycomb-like structures. Using Ultraviolet−visible spectroscopy, low critical solution temperature for HPG-g-PNVCL was observed at 34 °C, which is close to the rheology gel point at 33.5 °C. The thermoreversibility of HPG-g-PNVCL was proved by rheological analysis. The HPG-g-PNVCL hydrogel was employed for slow release of the drug molecule. Ciprofloxacin, a commonly known antibiotic, was used for sustainable release from the HPG-g-PNVCL hydrogel as a function of time at 37 °C because of viscous nature and thermogelation of the copolymer. In vitro cytotoxicity study reveals that the HPG-g-PNVCL thermogelling polymer works as a biocompatible scaffold for osteoblastic cell growth. Additionally, in vitro biomineralization study of HPG-g-PNVCL/n-HA/DVS was conducted using a simulated body fluid, and apatite-like structure formation was observed by SEM.

Platinum electrodes are commonly used electrocatalysts for oxygen reduction reactions (ORR) in fuel cells. However, this material is not economical due to its high cost and scarcity. We prepared an Mn(III) catalyst supported on graphene and further coated with polydopamine, resulting in superior ORR activity compared to the uncoated PDA structures. During ORR, a peak potential at 0.433 V was recorded, which is a significant shift compared to the uncoated material’s −0.303 V (both versus SHE). All the materials reduced oxygen in a wide pH range via a four-electron pathway. Rotating disk electrode and rotating ring disk electrode studies of the polydopamine-coated material revealed ORR occurring via 4.14 and 4.00 electrons, respectively. A rate constant of 6.33 × 10⁶ mol⁻¹s⁻¹was observed for the polydopamine-coated material–over 4.5 times greater than the uncoated nanocomposite and superior to those reported for similar carbon-supported metal catalysts. Simply integrating an inexpensive bioinspired polymer coating onto the Mn-graphene nanocomposite increased ORR performance significantly, with a peak potential shift of over +730 mV. This indicates that the material can reduce oxygen at a higher rate but with lower energy usage, revealing its excellent potential as an ORR electrocatalyst in fuel cells.

Nitrophenols (NPs) and related derivatives are industrially important chemicals, used notably to synthesize pharmaceuticals, insecticides, herbicides, and pesticides. However, NPs and their metabolites are highly toxic and mutagenic. They pose a serious threat to human health and ecosystem. Current work was undertaken to develop a suitable visible-light active catalyst for the sustainable and efficient mineralization of NPs in an aqueous environment. Nanocrystalline cellulose (NCs)-based nitrogen-doped titanium dioxide and carbonaceous material (N-TiO₂/C) was synthesized by pyrolysis and sol–gel methods using NCs, polydopamine, and TiO₂. The synthesized N-TiO₂/C was characterized using different analytical techniques. Photocatalytic degradation of NPs under visible light indicated that acidic pH (3) was most suitable for the optimal degradation. 4-NP degradation followed both pseudo-first-order (R² = 0.9985) and Langmuir–Hinshelwood adsorption kinetic models (adsorption constant, K_LH = 1.13 L mg^–1). Gas chromatography–mass spectrometry and ion chromatography analysis confirmed the total mineralization of 4-NP into smaller molecular fragments such as acids, alcohols, and nitrates. The total organic carbon showed that 67% of total carbon present in 4-NP was mineralized into CO₂ and CO. The catalyst was recycled for five consecutive cycles without losing its catalytic activities. The degradation mechanism of NPs with N-TiO₂/C was also explored.