Herein, 10-fold electrochemiluminescence (ECL) enhancement from a porous SnO 2 nanocrystal (SnO 2 NC) xerogel (vs discrete SnO 2 NCs) was first observed with NO 3 − as a novel coreactant. This new booster phenomenon caused by pore characteristic was defined as "pore confinement-induced ECL enhancement", which originated from two possible reasons: First, the SnO 2 NC xerogel with hierarchically porous structure could not only localize massive luminophore near the electrode surface, more importantly, but could accelerate the electrochemical and chemiluminescence reaction efficiency because the pore channels of xerogel could promote the mass transport and electron transfer in the confined spaces. Second, the NO 3 − could be in situ reduced easily to the active nitrogen species by means of the pore confinement effect, which could be served as a new coreactant for nanocrystal-based ECL amplification with the excellent stability and good biocompatibility. As a proof of concept, a facile and sensitive sensing platform for SO 3 2− detection has been successfully constructed upon effectively quenching of SO 3 2− toward the SnO 2 NC xerogel/NO 3 − ECL system. The key feature about this work presented a grand avenue to achieve the strong ECL signal, especially from weak emitters, which gave a fresh impetus to the construction of new-generation of surface-confined ECL platform with potential applications in ECL imaging and sensing.
Active macromolecular free radicals were generated on polypropylene (PP) fiber surfaces by argon plasma irradiation, and surface-modified PP fibers (PP-g-St fibers) were prepared by in situ grafting reaction of styrene monomers (St). The prepared samples were characterized by Fourier transform infrared, NMR, X-ray photoelectron spectroscopy, scanning electron microscopy, and thermogravimetric analysis. Effects of reaction parameters on grafting percentage were studied, and adsorption capacities of PP-g-St fibers for benzene, toluene, and xylene (BTX) were evaluated. Regeneration adsorption efficiencies after adsorption of pure BTX and BTX emulsion and solution in water were explored. The results indicated that, using pure St as the monomer, the optimum input power, irradiation time, and grafting reaction time are 90 W, 3 min, and 3 h, respectively, and the grafting percentage of St reached 5.7% when pure St was used. The characterization results demonstrated that St was grafted onto the surface of the PP fibers. Compared to pristine PP fibers, the adsorption capacities of PP-g-St fibers toward toluene and xylene emulsions and solutions in water increased. In addition, regeneration adsorption efficiencies of modified fibers remained >90% after six cycles of regeneration adsorption experiments, which showed excellent regeneration ability.
Zinc oxide nanoparticles (ZnO NPs) are used as antifungal agents and imparted in starch paste. The zinc oxide nanoparticles are synthesized using starch as a stabilizing agent under sonochemical irradiation, and then used in the preparation of ZnO NPs‐based starch paste. The effects of starch and ultrasonic irradiation on the formation of ZnO NPs are subsequently investigated. Characterization by X‐ray diffraction and transmission electron microscopy reveals that ZnO NPs synthesized under an optimal condition are highly dispersed and well‐defined crystals with diameters of approximately 5 nm. The antifungal performance of ZnO NPs‐based starch paste is evaluated under a high temperature and humidity environment, and is compared with traditional fungicides, alum, and pure terephthalic acid (PTA). In addition, the paste shows negligible toxicity and deterioration to the mechanical properties of the mounted paper. Lastly, the paper mounted with ZnO NPs‐based starch paste shows superior antifungal performance, an essential property protecting paper documents from mold growth, compared to pristine starch paste.
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