Highly Efficient Photocatalytic Degradation of Tetracycline by Modifying UiO-66 via Different Regulation Strategies.

Wastewater containing organic pollutants cause potential harm to the environment and human health. A series of zirconium-organic frameworks (UiO-66) and their composites were synthesized by solvothermal methods, including band gap adjustment, heterojunction construction, and metal ion doping. For the model pollutant tetracycline (TC), all of the prepared catalysts could achieve effective degradation of it. Therein, the degradation efficiency of tetracycline could reach 95% under the UV irradiation with the aid of the catalyst, in which the UiO-66-NDC was modified with P-C3N4. The free radical capture experiments demonstrated that the superoxide radical (•O2-) was the main oxidizing species for the photodegradation of tetracycline. Hence, the improvement strategy of the catalyst would provide some enlightenment for the development of more efficient photocatalysts for the degradation of organic dyes in wastewater.

g-C3N4-modified Zr-Fc MOFs as a novel photocatalysis-self-Fenton system toward the direct hydroxylation of benzene to phenol.

In order to explore a green, economic, and sustainable phenol production process, a heterojunction semiconductor materials g-C3N4/Zr-Fc MOF was synthesized via an in situ synthesis method. With the synergistic effect of photocatalysis and the Fenton effect, the composite could effectively catalyze the direct hydroxylation of benzene to phenol under visible light irradiation. The yield of phenol and the selectivity were 13.84% and 99.38% under the optimal conditions, respectively, and it could still maintain high photocatalytic activity after 5 photocatalytic cycles. Therefore, the designed photocatalysis-self-Fenton system has great potential in the field of the direct hydroxylation of benzene to phenol.

An efficient photocatalyst based on H5PMo10V2O40/UiO-66-NH2 for direct hydroxylation of benzene to phenol by H2O2.

To realize the direct hydroxylation of benzene to phenol by hydrogen peroxide, an efficient photoactive catalyst system was prepared by the recombination of H5PMo10V2O40 and UiO-66-NH2. The heterpolyacid was uniformly distributed on the UiO-66-NH2, and the combination was stable. The composite could effectively photocatalyze the direct hydroxylation of benzene to phenol by H2O2 in the mixture solution of acetonitrile and acetic acid. The yield and selectivity were 14.08% and 98.8% under the optimum condition, respectively. The performance of the catalyst still maintained well after 5 catalytic cycles. Hence, the investigated catalyst system might be applied in the field of hydroxylation of benzene to phenol.

Multifunctional graphene-based nanocomposites for simultaneous enhanced photocatalytic degradation and photothermal antibacterial activity by visible light.

A new strategy for the wastewater treatment was proposed by combining polyvinylpyrrolidone-functionalized silver nanoparticles with reduced graphene oxide (AgNPs-PVP@rGO) as a visible light-triggered photoactive nanocomposite. The nanocomposite with enhanced photocatalytic degradation and photothermal antibacterial activity can simultaneously decrease the content of organic pollutants and bacteria in the wastewater under visible light irradiation. The efficiency of photocatalytic degradation can be significantly improved by the conjugation of AgNPs onto the rGO surface. The water solubility and dispersion of nanocomposite can be increased via PVP functionalization, without stirring during the photocatalytic process. Under the optimal synthesis condition, AgNPs-PVP@rGO has a photocatalytic degradation efficiency of 90.1% for rhodamine B, which is 6.9 and 1.8 times higher than that of polyvinylpyrrolidone-functionalized silver nanoparticles and rGO alone, respectively. More importantly, the degradation efficiency of optimal AgNPs-PVP@rGO sol on rhodamine B is significantly higher than that of its block suspension in the same amount, indicating that the sol with more specific surface area is conducive to the photocatalytic reaction. Meanwhile, the AgNPs-PVP@rGO with excellent photothermal activity can effectively inhibit the bacterial growth. This functional modification of graphene provides a new strategy for simultaneous treatment of multiple pollutants in wastewater. The AgNPs-PVP@rGO nanocomposites for simultaneous enhanced photocatalytic degradation and photothermal antibacterial activity by visible light.

Ag-Conjugated graphene quantum dots with blue light-enhanced singlet oxygen generation for ternary-mode highly-efficient antimicrobial therapy.

The increasing prevalence of antibiotic resistance highlights the need for new antibacterial drugs and, in particular, the development of alternative approaches such as photodynamic therapy (PDT) and photothermal therapy (PTT) to manage this growing issue. In the present study, a broad-spectrum antibacterial system was produced in which Ag nanoparticle-conjugated graphene quantum dots (GQD-AgNP) were utilised as a blue light-enhanced nanotherapeutic for efficient ternary-mode antimicrobial therapy. The successful conjugation of AgNPs onto the surface of GQDs can significantly improve the production of reactive oxygen species in light-activatable GQDs and the transformation of light energy to hyperthermia with high efficiency. There was a remarkable increase in the sample temperature of nearly 40 °C via photoexcitation after only 10 min of 450 nm laser exposure (14.2 mW cm-2). The hybrids exhibited much more efficient bactericidal capability against both Gram-negative and Gram-positive bacteria compared with GQDs alone, using 450 nm light irradiation. This is likely a consequence of their enhanced PDT, concomitant PTT, and the synergistic function of AgNPs. The antibacterial mechanism of the new-style nanocomposites was found to irreversibly destroy the bacterial membrane structure, leading to the leaking out of the cytoplasmic contents and the death of the bacteria. At low doses, the biocompatible GQD-AgNP hybrids promoted healing in bacteria-infected rat wounds, with negligible adverse impact to the normal tissue, indicating a promising future for combined photodynamic and photothermal antibacterial applications in clinical medicine.

Methyl (R)-2-(2-chloro-phen-yl)-2-(3-nitro-phenyl-sulfon-yloxy)acetate.

The reaction between methyl (R)-2-(2-chloro-phen-yl)-2-hy-droxy-acetate and 3-nitro-benzene-sulfonyl chloride gave the title compound, C(15)H(12)ClNO(7)S, which is a promising inter-mediate for the synthesis of Clopidrogel, an anti-platelet drug used in the prevention of strokes and heart attacks. In the crystal, mol-ecules are linked through C-H⋯O interactions, and there is also a short Cl⋯O contact present [Cl⋯O = 3.018 (2) Å].

Surface-initiated ATRP of HEA from nanocrystal alpha-Fe2O3 under ultrasonic irradiation.

Core/shell poly(beta-hydroethyl acrylate) (PHEA) encapsulated nanocrystal alpha-Fe2O3 nanospheres (Fe2O3@PHEA) were successfully prepared by the surface-initiated atom transfer radical polymerization (SI-ATRP) of beta-hydroethyl acrylate (HEA), a functional monomer, from the surfaces of the nanocrystal Fe2O3 modified with bromo-acetamide groups with the catalysts of 1,10-phenanthroline and Cu(I)Br under ultrasonic irradiation at room temperature in water. The products, Fe2O3@PHEA, were characterized by elemental analysis (EA), FT-IR, XRD, XPS and TEM. The percentage of grafting (PG%) of 38.95% and the conversion of HEA (C%) of 14.29% at room temperature for 6 h with ultrasonic irradiation were higher than the 22.41% and 8.22%, respectively, found for samples prepared by electromagnetic stirring. This demonstrated that the ultrasonic irradiation improves the SI-ATRP of HEA.