Carbon dots-modified paper-based chemiluminescence device for rapid determination of mercury (II) in cosmetics.

Here, a simple and portable paper-based analytical device (PAD) based on the inherent capability of carbon quantum dots (CQDs) to serve as a great emitter for the bis(2,4,6-trichlorophenyl)oxalate (TCPO)-hydrogen peroxide (H2O2) chemiluminescence (CL) reaction is introduced for the detection of harmful mercury ions (Hg2+ ). The energy is transferred from the unstable reaction intermediate (1,2-dioxetanedione) to CQDs, as acceptors, and an intensive orange-red CL emission is generated at ~600 nm, which is equal to the fluorescence emission wavelength of CQDs. The analytical applicability of this system was examined for the determination of Hg2+ . It was observed that Hg2+ could significantly quench the produced emission, which can be attributed to the formation of a stable and nonluminescent Hg2+ -CQDs complex. Accordingly, a simple and rapid PAD was established for monitoring Hg2+ , with a limit of detection of 0.04 µg ml-1 . No interfering effect on the signal was found from other examined cations, indicating the acceptable specificity of the method. The designed assay was appropriately utilized to detect Hg2+ ions in cosmetic samples with high efficiency. It was characterized by its low cost, ease of use, and was facile but accurate and high selective for the detection of Hg2+ ions. In addition, the portability of this probe makes it suitable for on-site screening purposes.

A review of recent developments based on chemiluminescence detection systems for pesticides analysis.

Chemiluminescence is one of the most coveted methods for sensitive determination of pesticides in food and environmental samples. To date, many methods have been developed for qualitative and quantitative analysis of pesticides, ranging from traditional to advanced methods. This study outlines the progress in the conventional and advanced analytical methods, coupled to a chemiluminescence detection system, that are employed for the determination of pesticides in food and environmental samples. Different analytical methods including chromatographic methods, flow-based systems, and paper-based systems are reviewed in this paper. As well, new advances in the application of nanomaterials, aptamer, and molecularly imprinted polymers are highlighted. We also address the challenges and difficulties associated with these methods. Finally, we highlight the future direction in this active field of research.

A paper-based chemiluminescence detection device based on S,N-doped carbon quantum dots for the selective and highly sensitive recognition of bendiocarb.

Bendiocarb, a type of carbamate pesticide, plays a crucial role in controlling a wide range of pests. Due to its harmful impact on humans and the environment, the need for inexpensive, portable, efficient and easy-to-use analytical devices has become essential. In this study, an environmentally friendly paper-based analytical device (PAD) with a chemiluminescence (CL) sensing platform was investigated and characterized for the facile, reliable and sensitive detection of the bendiocarb pesticide. It is based on the enhancing effect of SO32- on the CL reaction of sulfur, nitrogen-doped carbon quantum dots (S,N-CQDs)-KMnO4 in acidic media. According to the experiments, S,N-CQDs and SO32- both are oxidized by KMnO4 to generate (S,N-CQDs*) and (SO2*) in their excited states, emitting at 510 nm. This indicates that an energy transfer process is taking place from SO2* to S,N-CQDs, resulting in a remarkably intensified CL emission. Interestingly, another emission was also observed around 660 nm contributing to about 20 to 25% of the total CL emission. This emission is related to the Mn2+* species produced by reducing MnO4-. The established multi-emission CL system was tested for analytical applications. Under optimal experimental conditions, a good linear relationship was observed between the bendiocarb concentration and the CL intensity of the established CL system. The linear detection range was 0.1-10 µg mL-1, with a limit of detection (LOD) of 0.02 µg mL-1. Finally, the method was successfully applied for the measurements of bendiocarb in water and juice samples. The obtained recovery values (97.5-105.5) verified the suitable accuracy of the results.