RESUMO
A portable and simple method was developed for on-site selective determination of As(III) based on the SERS signal of As(III)-O vibration. The method relies on the synergistic effect of nanoparticles aggregation and analyte adsorption. Experimental results demonstrated that phosphate replaced the ligands of HH@Ag NPs, which in turn facilitated the adsorption of As(III) on the surface of HH@Ag NPs. The phosphate was introduced as an agglomerating agent to improve the detection ability of the method for As(III). The method shows good selectivity and linear relationship between 5 × 10-8 and 0.8 × 10-6 M, with the detection limit of 1.8 × 10-9 M. The method was applied to actual water samples and successfully detected As(III), indicating that the method could have application potential in actual detection scenarios.
Assuntos
Arsênio/análise , Nanopartículas Metálicas/química , Fosfatos/química , Prata/química , Análise Espectral RamanRESUMO
An enhanced ratiometric fluorescence sensor was built for on-site visual detection of doxycycline (DOX) through the interaction with bovine serum albumin on the surface of red emissive copper nanoclusters. Upon the addition of weakly fluorescent DOX, the red fluorescence from copper nanoclusters gradually decreased through the inner-filter effect (IFE), while a green fluorescence appears and significantly increases, forming an interesting fluorescent isosbestic point, which was assigned to DOX due to sensitization effect of bovine serum albumin. On the basis of this ratiometric fluorescence, the system possessed good limit of detection (LOD) of 45 nM and excellent selectivity for DOX over other tetracyclines. Based on these findings, a paper-based sensor has been fabricated for distinct visual detection of trace DOX and combined with smartphone color recognizer for quantitative detection of DOX (LOD = 83 nM). This method shows broad application prospects in environmental monitoring and food safety.
Assuntos
Cobre , Nanopartículas Metálicas , Antibacterianos , Doxiciclina , Soroalbumina Bovina , Espectrometria de Fluorescência/métodos , TetraciclinasRESUMO
The nondestructive characterization of the mixing state of individual fine particles using the traditional single particle analysis technique remains a challenge. In this study, fine particles were collected during haze events under different pollution levels from September 5 to 11 2017 in Beijing, China. A nondestructive surface-enhanced Raman scattering (SERS) technique was employed to investigate the morphology, chemical composition, and mixing state of the multiple components in the individual fine particles. Optical image and SERS spectral analysis results show that soot existing in the form of opaque material was predominant during clear periods (PM2.5 ≤ 75 µg/m3). During polluted periods (PM2.5 > 75 µg/m3), opaque particles mixed with transparent particles (nitrates and sulfates) were generally observed. Direct classical least squares analysis further identified the relative abundances of the three major components of the single particles: soot (69.18%), nitrates (28.71%), and sulfates (2.11%). A negative correlation was observed between the abundance of soot and the mass concentration of PM2.5. Furthermore, mapping analysis revealed that on hazy days, PM2.5 existed as a core-shell structure with soot surrounded by nitrates and sulfates. This mixing state analysis method for individual PM2.5 particles provides information regarding chemical composition and haze formation mechanisms, and has the potential to facilitate the formulation of haze prevention and control policies.
Assuntos
Poluentes Atmosféricos , Material Particulado , Aerossóis/análise , Poluentes Atmosféricos/análise , Pequim , China , Monitoramento Ambiental , Tamanho da Partícula , Material Particulado/análise , Estações do Ano , Análise Espectral RamanRESUMO
Selective and sensitive determination of ceftriaxone sodium (CTR) trace residues is of great importance for food safety and environmental protection. Herein, a determination method based on ratiometric fluorescence and colorimetric method with nitrogen-rich carbon dots as fluorophore is reported. The functional surfaces of indole-derived carbon dots (I-CDs) containing nitrogen and carbon groups can be selectively bound to CTR by electrostatic forces, leading to a hindered conjugation system and deprotonation of the amine on the pyrrole ring, resulting in a distinct variety in fluorescence and absorption wavelength and intensity. With the addition of CTR, the fluorescence at 577 nm can be selectively quenched, accompanied by a new emission peak appeared at 507 nm. The limits of detection (LODs) were estimated to be 19.7 nM and 78.0 nM based on the ratiometric fluorescence method and colorimetric method, respectively. Finally, the in situ visual quantitative determination of CTR using this nanosensor was achieved by combining with the color recognizer of a smartphone, and the method was further validated by spike and recovery test in real water samples including milk, seawater, and tap water.
Assuntos
Ceftriaxona , Pontos Quânticos , Carbono/química , Nitrogênio , Pontos Quânticos/química , Corantes Fluorescentes/química , ÁguaRESUMO
2,4,6-trinitrophenyl phenol (TNP) and dichromate (Cr2O72-) have serious toxicological effects on environment. Therefore, it is very important to detect and remove TNP and Cr2O72- in environmental matrix. In this work, a dual-functional UiO type metal-organic framework (Zr-Sti) was synthesized for simultaneous detection and removal of those pollutants in aqueous solution. As for detection, Zr-Sti exhibited sensitive and selective fluorescence response to TNP and Cr2O72- with detection limit below µM level, and possible mechanism behind was proposed and partially supported by experiment data. In addition, adsorption capacity of the prepared Zr-Sti for TNP and Cr2O72- was further investigated to evaluate its performance in pollutant removal from aqueous solution, and the mechanism behinds the obtained high removal efficiency was proposed. These results together with the satisfied recovery for simultaneous detection of TNP and Cr2O72- in real sample, indicate the potential of the prepared Zr-Sti material in the field of environment monitoring and remediation.
RESUMO
Cuprous ion is an essential element for human life activities. However, excessive cuprous can cause dysfunction of the human body system. To help explain this evolving biology, we report a fluorescent probe for detecting unstable Cu(I). Cu(I) undergoes a metal complexation reaction with the sulfur element in the probe, resulting in a photoelectron transfer (PET) effect. The probe fluorescence is greatly suppressed, and rapid and selective visual detection of Cu(I) in the inorganic environment is realized. There is also a good linear relationship between the probe fluorescence intensity and the Cu(I) concentration (R2 = 0.992), which can realize the quantitative detection of Cu(I). When the probe concentration is 0.1 µM, the detection limit is 15 nM, and the detection limit of the visual method is as low as 0.1 µM. This work provides a valuable starting point for real-time monitoring of the Cu(I) concentration in a human anaerobic environment based on active probes.