Seafood waste derived Pt/Chitin nanocatalyst for efficient hydrogenation of nitroaromatic compounds.

The fabrication of reliable, reusable and efficient catalyst is crucial for the conversion of nitroaromatic compounds into more chemically valuable amine-based molecules. In this study, a series of chitin supported platinum (Pt) catalysts with high catalytic activity, stability, and reusability were developed by using chitin derived from seafood waste as raw materials. The catalytic performance differences among these catalysts activated by different methods were investigated by hydrogenation of nitroaromatic compounds. The results showed that the multilayer hierarchical pore structure and abundance of hydroxyl and acetamido groups in chitin provided ample anchoring sites for Pt nanoparticles (NPs), ensuring the high dispersion of Pt NPs. Moreover, the interconnected channels between chitin nanofibrous microspheres facilitated rapid transport of reaction substrates. The best Pt/Chitin catalyst exhibited excellent catalytic activity and broad substrate applicability in hydrogenation of nitroaromatic compounds. Significantly, even after 20 runs, no discernible deactivation of activity was observed, demonstrating exceptional catalytic reusability. The application of seafood waste-based catalysts is conducive to the development of a green/sustainable society.

Fabrication of Biomass Derived Pt-Ni Bimetallic Catalyst and Its Selective Hydrogenation for 4-Nitrostyrene.

The hydrogenation products of aromatic molecules with reducible groups (such as C=C, NO2, C=O, etc.) are relatively critical intermediate compounds in fine chemicals, but how to accurately reduce only specific groups is still challenging. In this work, a bimetallic Pt-Ni/Chitin catalyst was prepared for the first time by using renewable biomass resource chitin as support. As the carrier, the chitin was constructed into porous nanofibrous microspheres through the sol-gel strategy, which was favorable for the adhesion of nano-metals and the exchange of reactive substances due to its large surface area, porous structure, and rich functional groups. Then the Pt-Ni/Chitin catalyst was applied to selective hydrogenation with the model substrate of 4-nitrostyrene. As the highly dispersed Pt-Ni NPs with abundant exposed active sites and the synergistic effect of bimetals, the Pt-Ni/Chitin catalyst could efficiently and selectively hydrogenate only NO2 or C=C with yields of ~99% and TOF of 660 h-1, as well as good stability. This utilization of biomass resources to build catalyst materials would be important for the green and sustainable chemistry.

Cellulose derived Pd nano-catalyst for efficient catalysis.

Using green, environmentally friendly and resource-rich cellulose as a raw material, a ligand-free and highly dispersed palladium (Pd) nano-catalyst was successfully prepared in a facile way. A variety of characterization results showed that the Pd nanoparticles (NPs) were uniformly spread on the cellulose nanoporous microspheres, with an average particle size of ∼2.75 nm. As a carrier, cellulose microspheres with nanoporous structure and rich -OH groups greatly promoted the attachment and distribution of the highly dispersed Pd NPs, along with the diffusion and exchange of reactants, so as to greatly promote the catalytic activity. In the Suzuki-Miyaura coupling reaction, the catalyst of C-Pd exhibited excellent catalytic activity (TOF up to 2126 h-1), broad applicability, and good recyclability with almost no active loss in 6 continuous runs. This utilizing of bioresources to build catalyst materials is important for sustainable chemistry.

Confined transformation of trifunctional Co2(OH)2CO3 nanosheet assemblies into hollow porous Co@N-doped carbon spheres for efficient microwave absorption.

Carbonaceous-magnetic composites are the most appealing candidates for electromagnetic wave absorption, and creating hollow interiors and nanopores in the composites is commonly recognized as an essential strategy to reinforce their overall performances. Herein, we propose a spatial confinement strategy mediated by Co2(OH)2CO3 nanosheet assemblies for achieving highly dispersed Co nanoparticles into hollow porous N-doped carbon shells (HP-Co@NCS). Systematic multi-technique characterizations indicate that the Co2(OH)2CO3 nanosheet assemblies simultaneously play a trifunctional role during the synthesis, including Co source, template of the hollow interior cavities, and micro-/mesopore porogen. The chemical composition can be modulated by simply varying the ratio of Co2(OH)2CO3 and carbon source (dopamine). The optimized HP-Co@NCS absorber exhibits a well-defined hollow structure and unprecedented high porosity (specific surface area of 742 m2 g-1) even with a high metallic Co content of 35.8 wt%. These profitable structural characteristics can facilitate incident EM waves penetrating the absorber's interior and promoting multiple reflections and scattering. Therefore, the HP-Co@NCS absorber exhibits efficient microwave absorption ability with a minimum reflection loss of -39.0 dB at a thin thickness of 2.5 mm and an effective absorption bandwidth up to 5.5 GHz (12.5-18.0 GHz) at a thin thickness of 2.0 mm. This work provides a new methodology to design advanced carbonaceous-magnetic composite materials with hollow porous structures for microwave absorption.

Monodispersed CuO nanoparticles supported on mineral substrates for groundwater remediation via a nonradical pathway.

Nonradical oxidation based on singlet oxygen (1O2) has attracted great interest in groundwater remediation due to the selective oxidation property and good resistance to background constituents. Herein, recoverable CuO nanoparticles (NPs) supported on mineral substrates (SiO2) were prepared by calcination of surface-coated metal-plant phenolic networks and explored for peroxymonosulfate (PMS) activation to generate 1O2 for degrading organic pollutants in groundwater. CuO NPs with a close particle size (40 nm) were spatially monodispersed on SiO2 substrates, allowing highly exposure of active sites and consequently leading to outstanding catalytic performance. Efficient removal of various organic pollutants was obtained by the supported CuO NPs/PMS system under wide operation conditions, e.g., working pH, background anions and natural organic matters. Chemical scavenging experiments, electron paramagnetic resonance tests, furfuryl alcohol decay and solvent dependency experiments confirmed the formation of 1O2 and its dominant role in pollutants removal. In situ characterization with ATR-FTIR and Raman spectroscopy and computational calculation revealed that a redox cycle of surface Cu(II)-Cu(III)-Cu(II) was responsible for the generation of 1O2. The feasibility of the supported CuO NPs/PMS for actual groundwater remediation was evaluated via a flow-through test in a fixed-bed column, which manifested long-term durability, high mineralization ratio and low metal ion leaching.