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CO oxidative coupling to dimethyl oxalate (DMO) is an important approach for the product of ethylene glycol and CO elimination. In this work, the Co doped Pd/Al2O3 nanocatalyst was highly effective for CO oxidative coupling and enhanced remarkably CO conversion and the formation of DMO. The maximum DMO STY reached 1082 g L−1 h−1 over the Pd/Al2O3@1/20Co catalyst at 130 °C for 2 h under the space velocity of 3000 h−1, which is two times higher than that over the Pd/Al2O3 catalyst. The Co modification and its influence on the structure of the Pd/Al2O3 catalyst were also studied systematically by XRD, TEM, CO‐TPD, N2 physical adsorption and XPS techniques. An appropriate Co doing was confirmed to promote distinctly the generation of smaller Pd particles and the adjustment of the adsorption or activation of CO over the catalyst. A positive interaction between Pd nanoparticles and the modulated support with Co doping was demonstrated and favored the enhanced activity of the catalyst for the reaction. [ABSTRACT FROM AUTHOR]

Catalytic conversion of glucose to lactic acid is a green promising strategy for the effective utilization of biomass‐derived carbohydrates to generate valuable chemicals. The generation of lactic acid would also be distinguishing in different reaction atmospheres. In this work, we firstly investigated the decomposition of lactic acid and glucose transformation to lactic acid in H2. No obvious decomposition of lactic acid was observed in H2. The activity testing results showed that glucose could be completely converted over the selected hydroxides, while the formation of lactic acid was closely related to the alkalinity of hydroxide. The yield of lactic acid was remarkably obtained to be 87 % over Ca(OH)2 at 220 °C for 3 h. Stronger alkalinity of the catalyst would facilitate glucose isomerization to fructose, and then easily be transformed into dihydroxyacetone or glyceraldehyde intermediates through reverse aldol condensation, which is beneficial to the generation of lactic acid. [ABSTRACT FROM AUTHOR]

Guided bone regeneration (GBR) is a frequently used technique for patients with insufficient alveolar bone. The discovery of bone substitutes that can enhance osteogenesis is critical for GBR. Graphdiyne (GDY), a newly discovered carbon‐based nanomaterial, has been recognized as the most stable allotrope of acetylene carbon and is anticipated to be able to promote osteogenesis. Whereas it still remains unknown whether it could enhance osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs). In this study, GDY was modified with polyethylene glycol (PEG) and the influences of GDY‐PEG at different concentrations on BMSCs cell growth and osteogenic differentiation were researched for the first time. In this study, we found that GDY‐PEG at low concentration possessed premium bio‐compatibility and revealed evident facilitation of BMSCs osteogenic differentiation. The cell growth and osteogenic differentiation of BMSCs treated with GDY‐PEG were dose‐dependent. GDY‐PEG at 1 μg/mL demonstrated the optimal promoting effects of BMSCs osteogenic differentiation. Moreover, the regulating effect of BMSCs osteogenic differentiation by GDY‐PEG might be associated with the Wnt/β‐catenin signaling pathway. In all, the present study indicated a novel application of GDY in promoting bone tissue regeneration, providing a novel biomaterial for bone augmentation in clinics. [ABSTRACT FROM AUTHOR]

Amino-functionalized monodisperse polymeric microspheres have great significance in water remediation. Herein, polypyrrole (PPy)-modified silica-coated magnetic monodispersed emulsion sphere (MES) microspheres (MES@Fe3O4@SiO2-PPy, MFSP) were successfully prepared via in situ polymerization for the adsorption of hexavalent chromium in an aqueous solution. The magnetism of MFSP enabled fast separation under an applied magnetic field. The results showed that MFSP exhibited outstanding adsorption for Cr(VI) (301.2 mg g−1 at pH 2.0), which followed the pseudo-second-order kinetic and Langmuir isotherm models. Moreover, the MFSP can be reused in the adsorption–desorption cycle by simple elution, and the removal rate of Cr(VI) by MFSP remained above 91% after five consecutive cycles. Combined with XPS, EDS, and Zeta potential measurement for adsorption mechanism analysis, it was concluded that the removal of Cr(VI) could be attributed to both adsorption and reduction. The combination of good adsorption performance and magnetic separation makes MFSP a promising candidate for the removal of low-concentration metal ions. [ABSTRACT FROM AUTHOR]