Unveiling the overlooked threat: antibiotic resistance in groundwater near an abandoned sulfuric acid plant in Xingyang, China.

Groundwater near a sulfuric acid plant in Xingyang, Henan, China was sampled from seven distinct sites to explore the prevalence of antibiotic resistance genes (ARGs) and mobile genetic elements (MGEs). Results showed that genes aadA, blaCTX-M, tetA, qnrA, and sul1 were detected with 100% frequency followed by aac(6')-Ib (85.71%), ermB (85.71%), and tetX (71.42%). Most abundant ARGs were sul1 in LSA2 (1.15 × 1011 copies/mL), tetA in LSA6 (4.95 × 1010 copies/mL), aadA in LSA2 (4.56 × 109 copies/mL), blaCTX-M in LSA4 (1.19 × 109 copies/mL), and ermB in LSA5 (1.07 × 109 copies/mL). Moreover, in LSA2, intl1 as a marker of class 1 integron emerged as the most abundant gene as part of MGE (2.25 × 1011 copies/mL), trailed by ISCR1 (1.57 × 109 copies/mL). Environmental factors explained 81.34% of ARG variations, with a strong positive correlation between the intl2 and blaCTX-M genes, as well as the ISCR1 gene and qnrA, tetA, intl2, and blaCTX-M. Furthermore, the intI1 gene had a strong positive connection with the aadA, tetA, and sul1 genes. Moreover, the aac(6')-Ib gene was associated with As, Pb, Mg, Ca, and HCO3-. The intl2 gene was also shown to be strongly associated with Cd. Notably, network analysis highlighted blaCTX-M as the most frequently appearing gene across networks of at least five genera. Particularly, Lactobacillus, Plesiomonas, and Ligilactobacillus demonstrated correlations with aadA, qnrA, blaCTX-M, intI2, and ISCR1. Based on 16S rRNA sequencing, the dominant phyla were Proteobacteria, Firmicutes, Bacteroidota, Acidobacteriota, and Actinobacteriota, with dominant genera including Pseudomonas, Ligilactobacillus, Azoarcus, Vogesella, Streptococcus, Plesiomonas, and Ferritrophicum. These findings enhance our understanding of ARG distribution in groundwater, signaling substantial contamination by ARGs and potential risks to public health.

Fabrication of a Novel Z-Scheme AgBiO3/BiOCl Heterojunction with Excellent Photocatalytic Performance towards Organic Pollutant.

A novel and highly efficient photocatalyst of a AgBiO3/BiOCl heterojunction has been developed via a facile water bath and in situ precipitation method. The photocatalytic activities of the catalysts were investigated by the degradation of ciprofloxacin (CIP) under visible-light irradiation (>420 nm). The experiment results revealed that the photocatalytic performance of the optimized AgBiO3/BiOCl heterojunction was much higher than pure AgBiO3 and BiOCl. The degradation efficiency of the as-prepared AgBiO3/BiOCl heterojunction (ABC-30) for CIP could reach 88% within 160 min, with 2.89 and 3.76 times higher activity than pure AgBiO3 and BiOCl, respectively. The improved photocatalytic performance of AgBiO3/BiOCl was attributed to the synergistic effect of the enhanced light absorption range and effective separation and transfer of the photo-induced charge carrier. The optimized heterojunction showed broad-spectrum catalytic activities towards various organic contaminants. The degradation efficiencies varied with the nature of the pollutant and decreased in the following order: Lanasol Red 5B (100%) > methyl orange (99%) > methylene blue (98%) > tetracycline (92%) > ciprofloxacin (88%) > ofloxacin (85%) > norfloxacin (78%) > rhodamine B (59%) > metronidazole (43%) > phenol (40%) > carbamazepine (20%). Furthermore, the trapping experiments and ESR indicated that superoxide radicals and holes were the main reactive species.

Synthesis of Novel Kaolin-Supported g-C3N4/CeO2 Composites with Enhanced Photocatalytic Removal of Ciprofloxacin.

Herein, novel ternary kaolin/CeO2/g-C3N4 composite was prepared by sol-gel method followed by hydrothermal treatment. The self-assembled 3D "sandwich" structure consisting of kaolin, CeO2 and g-C3N4 nanosheets, was systematically characterized by appropriate techniques to assess its physicochemical properties. In the prerequisite of visible-light irradiation, the removal efficiency of ciprofloxacin (CIP) over the kaolin/CeO2/g-C3N4 composite was about 90% within 150 min, 2-folds higher than those of pristine CeO2 and g-C3N4. The enhanced photocatalytic activity was attributed to the improved photo-induced charge separation efficiency and the large specific surface area, which was determined by electrochemical measurements and N2 physisorption methods, respectively. The synergistic effect between the kaolin and CeO2/g-C3N4 heterostructure improved the photocatalytic performance of the final solid. The trapping and electron paramagnetic resonance (EPR) experiments demonstrated that the hole (h+) and superoxide radicals (•O2-) played an important role in the photocatalytic process. The photocatalytic mechanism for CIP degradation was also proposed based on experimental results. The obtained results revealed that the kaolin/CeO2/g-C3N4 composite is a promising solid catalyst for environmental remediation.