Enriched photocatalytic and photoelectrochemical activities of a 2D/0D g-C3N4/CeO2 nanostructure.

Sunlight-powered photocatalysts made from CeO2 nanosized particles and g-C3N4 nanostructures were produced through a thermal decomposition process with urea and cerium nitrate hexahydrate. The preparation of g-C3N4, CeO2, and a binary nanostructured g-C3N4/CeO2 photocatalyst was done through a facile thermal decomposition method. The structural properties were analyzed using powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy (XPS). Photocatalyst properties were characterized by using crystal violet (CV), a UV-Vis spectrophotometer, photocurrent and electron impedance spectroscopy (EIS). The structural and morphological analyses revealed that the g-C3N4/CeO2 nanostructures significantly enhanced the photoactivity for CV dye degradation under simulated sunlight, with a degradation rate of 94.5% after 105 min, compared to 82.5% for pure g-C3N4 and 45% for pure CeO2. This improvement was attributed to the noticeable visible light absorption and remarkable charge separation abilities of the nanostructures. Additionally, the g-C3N4/CeO2 nanostructures showed notable PEC performance under simulated sunlight. This study presents an easy and efficient method for producing g-C3N4 photocatalysts decorated with semiconductor materials and provides insights for designing nanostructures for photocatalytic and energy applications.

Selective synthesis of 1,6-anhydro-ß-d-mannopyranose and -mannofuranose using microwave-assisted heating.

The dehydration of d-mannose and the demethanolization of methyl-α-d-mannopyranoside (MαMP) or methyl-α-d-mannofuranoside (MαMF) were examined using microwave-assisted heating for a 3-min irradiation at temperature from 120 to 280°C in ordinary or dry sulfolane without any catalyst. The microwave-assisted heating of MαMP and MαMF smoothly proceeded to selectively afford the anhydromannoses, 1,6-anhydro-ß-d-mannopyranose (AMP) and 1,6-anhydro-ß-d-mannofuranose (AMF), respectively, in high yields. For MαMP in ordinary sulfolane at 240°C, AMP was selectively obtained in the AMF:AMP ratio of 4:96, whereas AMF was the major product at the AMF:AMP ratio of 97:3 from MαMF in dry sulfolane at 220°C.

Synthesis, characterization, and lectin recognition of hyperbranched polysaccharide obtained from 1,6-anhydro-D-hexofuranose.

1,6-Anhydro-D-hexofuranoses, such as 1,6-anhydro-ß-D-glucofuranose (1), 1,6-anhydro-ß-D-mannofuranose (2), and 1,6-anhydro-α-D-galactofuranose (3), were polymerized using a thermally induced cationic catalyst in dry propylene carbonate to afford hyperbranched polysaccharides (poly1-3) with degrees of branching from 0.40 to 0.46. The weight-average molecular weights of poly1-3 measured by multiangle laser light scattering varied in the range from (1.02 to 5.84) × 10(4) g·mol(-1), which were significantly higher than those measured by size exclusion chromatography. The intrinsic viscosities ([η]) of poly1-3 were very low in the range from 4.9 to 7.4 mL·g(-1). The exponent (α) in the Mark-Houkwink-Sakurada equation ([η] = KM(α)) of the polymers was 0.20 to 0.33, which is <0.5. The steady shear flow of poly1-3 in an aqueous solution exhibited a Newtonian behavior with steady shear viscosities independent of the shear rate. These viscosity characteristics were attributed to the spherical structures of hyperbranched polysaccharides in an aqueous solution. Poly1-3 contained a high portion of terminal units of 31-43 mol % nonreducing D-hexopyranosyl and D-hexofuranosyl units, in which the D-hexofuranosyl units were 20-44 mol %. Moreover, poly1 and poly2 showed a strong interaction to Concanavalin A due to the cluster effect or multivalent effect of numerous nonreducing saccharide units on their surfaces with binding constants in the range from 1.7 × 10(4) to 2.7 × 10(5) M(-1).

Batch and column separation characteristics of copper-imprinted porous polymer micro-beads synthesized by a direct imprinting method.

Copper (II) ion-imprinted porous polymethacrylate micro-particles were prepared. Two functional monomers, methacrylic acid and vinyl pyridine, formed a complex with the template copper ion through ionic interactions. The self-assembled copper/monomer complex was polymerized in the presence of an ethylene glycol dimethacrylate cross-linker by a suspension method. After the imprinting sites were provided through removal of the template, the micro-porous particles, of approximate size 200 microm, were obtained for batch and column separation applications. The chemical structure and morphology of the Cu(II)-imprinted micro-porous particles were analyzed using FTIR, SEM, and BET. The adsorption capacity and adsorption kinetics of the imprinted beads for the template Cu(II) ion were significantly affected by particle size, copper ion concentration, pH, and flow rate of the feed solution. The imprinted particles showed high selectivity for the copper ion over other metal ions such as Ni and Zn. The selectivity of the present imprinted polymers for the copper ion was at least 10 times as high as those from commercial sources.