The generation of noise requires a noise source, transmission path, and passive acceptance target of noise, all of which are indispensable. Blocking the propagation path of noise is one of the available means when the existence of the noise source and passive receiving target cannot be addressed. This is an effective way to prevent noise pollution, often using sound insulation materials to block the path of noise transmission. In this work, composites with excellent sound insulation properties were designed and prepared. These composites, using epoxy resin (EP) as the matrix, polyethylene glycol (PEG), and hollow polystyrene spheres (HPS), were added to epoxy resin as a toughening agent and functional filler to prepare the ternary HPS/PEG/EP composites. The soundproofing results showed that when the thickness of the sample was 3 mm, the average sound transmission loss (STL) value of the neat EP and the HPS/PEG/EP composites with an HPS 32 vol% was up to 19.0 dB and 42.1 dB, and the STL values of the composites were increased by approximately 120% compared to the pure epoxy. When the sample was 10 mm thick, the average STL value of the HPS/PEG/EP composites with HPS 32 vol% contents was enhanced to 55.7 dB.

The double specific nuclease (DSN)-based methods for microRNAs (miRNAs) detection usually require the immobilization of DNA probes on a solid surface. However, such strategies have the drawbacks of low hybridization and cleavage efficiency caused by steric hindrance effect and high salt concentration on the solid surface. Herein, we proposed an immobilization-free method for miRNA detection on the basic of DSN-assisted signal amplification. The biotin- and fluorophore-labeled probes were captured by streptavidin-modified magnetic beads through streptavidin–biotin interactions, thus producing a poor fluorescence signal. Once the DNA probes were hybridized with target miRNA in solution to form DNA-miRNA duplexes, DNA stands in the duplexes would be selectively digested by DSN. The released target miRNA could initiate the next hybridization/cleavage recycling in the homogeneous solution, finally resulting in the release of numerous fluorophore-labeled fragments. The released fluorophores remained in solution and emitted strong fluorescence after treatment by the streptavidin-modified magnetic beads. The immobilization-free method achieved the assays of miRNA-21 with a detection limit down to 0.01 pM. It was employed to evaluate the expression levels of miRNA-21 in different cancer cells with satisfactory results.

Melamine polyphosphate (MPP) is a widely employed additive-type flame retardant for polyamide 6. Generally, a higher loading of MPP leads to improved flame retardancy of polyamide 6 composites. Nevertheless, excessive addition tends to cause problems such as flame-retardant migration, leakage, and exudation. Against this background, this work focuses on covalently grafting melamine polyphosphate onto the surface of carbon nanotubes via a facile chemical reaction, with the aim of alleviating the migration and leakage of the flame retardant in the polyamide 6 matrix. Carbon nanotubes (CNTs) were surface modified with a silane coupling agent (KH560) to obtain CNTs bearing epoxy groups (CNT-KH560). Subsequently, a ring-opening addition reaction was conducted between the CNT-KH560 and melamine polyphosphate (MPP) yielding carbon nanotubes with surface-bonded flame-retardant MPP (CNTM). Polyamide 6 composite slices (PA6/CNTM) were prepared via twin-screw extrusion blending and compounding and then by hot-press molding into test specimens. The modified carbon nanotubes were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis. The results confirmed the successful grafting of MPP onto the carbon nanotube surface, with a grafting degree of 9.1 g/100 g measured. The flame retardancy of the PA6/CNTM composites were evaluated through UL 94 vertical burning and limiting oxygen index (LOI) tests and cone calorimeter. These flame retardancy results indicated that when the content of flame-retardant-modified carbon nanotubes was 10 wt%, the PA6/CNTM10 composites achieved UL 94 V-2 and the limiting oxygen index increased from 24.5% of pure PA6 to 29.1%. The PHRR value of pure PA6 decreased from 750 kW/m² to 614 kW/m². This design of surface-grafted flame retardant provides a new strategy for the preparation and application of high-performance polyamide 6 flame-retardant composites.

Our work introduces a facile and efficient metal-free [3+3] annulation approach for the synthesis of polysubstituted pyridines via the reaction between β-enaminonitriles and β,β-dichloromethyl peroxides. This strategy operates under mild conditions, demonstrating broad substrate scope and excellent functional group tolerance. Mechanistic investigations suggest that the reaction proceeds through a Kornblum–De La Mare rearrangement followed by S_NV-type C-Cl bond cleavage and intramolecular cyclization/condensation. By circumventing the need for transition metal catalysts or radical initiators, our method offers practical utility in organic synthesis and provides a new avenue for the rapid construction of complex pyridine scaffolds.