Microplastics (MPs) and fungicides have been recognized as two main pollutants in ecological environments, especially in aqueous ecosystems. In this study, the adsorption behavior of three typical strobilurins (azoxystrobin, picoxystrobin, and pyraclostrobin) on polystyrene (PS) and polyethylene (PE) was investigated, and the effects of adsorption on the residual behavior and bioavailability of pyraclostrobin were evaluated. The results showed that MPs had strong adsorption capacity for the three kinds of strobilurins. Under similar conditions, the adsorption capacity was the highest for pyraclostrobin, followed by picoxystrobin and azoxystrobin, which was consistent with their octanol-water partition coefficients. Moreover, the adsorption capacity of PS was slightly higher than that of PE. The pH of aqueous solution had little effect on adsorption capacity, while an increase in ionic strength increased the adsorption capacity of azoxystrobin and picoxystrobin. The Fourier transform infrared spectra of MPs showed that no new chemical groups were formed during the adsorption process. Thus, it is speculated that hydrophobic interactions may be the driving force behind the adsorption of strobilurins on the MPs. Additionally, the adsorption of pyraclostrobin on MPs significantly reduced its residual amount in the aqueous solution, which reduced the adsorption and bioavailability of pyraclostrobin in black bean seedlings. The study provides effective information for environmental safety risk assessments with regard to the combined pollution risks of MPs and strobilurins.This work represents the use of N-3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxopropanenitrile as a cyanoacetylating agent for the synthesis of cyanoacetamide benzoic acid and benzophenone derivatives by two different methods, namely, conventional heating and ultrasonication. The cyanoacetamide derivatives were subjected to cyclization to produce N-substituted 2-pyridone derivatives under conventional heating and by an ultrasonic method as well. The ultrasonic method afforded the products in less reaction time with high yields and purities compared to the conventional method, as observed from their spectral data. N-(4-Carboxy phenyl)-4,6-dimethyl-3-cyano-2-pyridone was coupled with different amino acid esters by the OxymaPure/DIC methodology under traditional and ultrasonic conditions.  https://www.selleckchem.com/products/r-hts-3.html  Again, ultrasonication assisted the coupling step and afforded the products with higher yields and purities compared to the traditional method. Fourier transform infrared spectroscopy, NMR (1H and 13C), elemental analysis, and LC-MS were used to determine the structures of all compounds. Finally, a feature of this protocol is exploring the utilization of ultrasonication as an eco-friendly alternative conventional heating method for N-cyanoacylation and synthesis of N-substituted pyridinone derivatives and as a coupling method for the formation of an amide bond, which might be of interest for many researchers.A sol/gel curing method is used in this work to synthesize hybrid partially bio-based polyhydroxyurethanes (PHUs) from dicarbonates derived from glycerol and various diamines. The method consists of end-capping the PHU prepolymers with moisture-sensitive groups, so sealants and adhesives can be produced from partially sustainable hybrid PHUs (HPHUs), similar to their preparation from end-capped conventional polyurethanes. Diglycerol dicarbonate (DGC) is synthesized and polymerized with different diamines of various chain lengths, and the resulting structural and thermal properties of the PHUs are qualitatively and quantitively characterized. This characterization led to two potential candidates PHU 4, made of DGC and a poly(propylene glycol) diamine, and PHU 10, prepared from DGC and a poly(dimethylsiloxane) diamine. These polymers, with respective relative number-average molecular weights of 3200 and 7400 g/mol, are end-capped and left to cure under ambient lab conditions (22 °C and 40-50% humidity), and the curing processes are monitored rheologically. Notably, moisture curing does not require any catalyst. The chemical stability of the resulting hybrid PHUs (HPHUs) 4 and 10 in pure water is investigated to check the viability of applying them under outdoor conditions. Only HPHU 10 is found to be resistant to water and shows hydrophobicity with a contact angle of 109°. Tensile tests are conducted on HPHU 10 samples cured under lab conditions for a week and others cured for another week while being immersed in water. The mechanical properties, tensile strength and elongation at break, improve with the samples cured in water, indicating the high-water repellency of HPHU 10.In this study, novel ternary composites were prepared, including biodegradable poly(ethylene succinate) (PESu), poly(ethylene glycol) (PEG), and graphene oxide (GO). We have conducted a comprehensive study on whether GO can successfully promote the crystallization behaviors of PESu in the ternary composites. The results of isothermal crystallization demonstrated that with the increase of GO content in the composite (at a fixed PESu/PEG ratio), the Avrami rate constant k gradually increased, indicating that the crystallization rate was faster when GO was added to the composite. The same phenomenon was also found for nonisothermal crystallization. It was found that the Mo model can adequately describe the nonisothermal crystallization behaviors of the composites. The analyses demonstrated that the F(T) value estimated from the Mo model decreased when the GO content was increased. This result implied that GO promoted the nonisothermal crystallization of PESu in the ternary PESu/PEG/GO composites. Discussions on nucleation activity and microscopy observations confirmed that GO can act as a nucleation agent to further enhance the crystallization of the composites. The significant nucleation effect of GO on PESu in its novel ternary composite was first discovered in this study.β-Thujaplicin possess a variety of biological activities. The use of modified biological nanoparticles (NPs) to develop novel anti-influenza drugs has increased in recent years. Selenium nanoparticles (SeNPs) with antiviral activity have attracted increasing attention for biomedical intervention. Functionalized SeNPs by β-thujaplicin (Se@TP) surface modified with superior antiviral activity were synthesized in this study. Compared to a virus group (43%), when treated with Se@TP (88%), the cell survival rate of MDCK cells was 45% higher. Se@TP could inhibit H1N1 from infecting Madin-Darby canine kidney (MDCK) cells and block chromatin condensation and DNA fragmentation. Se@TP obviously prevented MDCK cells from generating reactive oxygen species. Furthermore, Se@TP prevents lung injury in H1N1-infected mice through eosin staining and hematoxylin in vivo. Mechanistic investigation revealed that Se@TP inhibited H1N1 influenza virus from infecting MDCK cells through induction of apoptosis via suppressing AKT and p53 signaling pathways through immunohistochemical assay.