Discrimination and simultaneous quantification of poly(ethylene terephthalate) and poly(butylene terephthalate) microplastics in environmental samples via gas chromatography-tandem mass spectrometry.

A method has been developed to quantify PET and PBT microplastics (MPs) based on depolymerization and detection of depolymerization products by gas chromatography-tandem mass spectrometry (GC-MS/MS) without a complex separation process from environmental samples. Under the optimal depolymerization conditions, PET and PBT were efficiently converted to ethylene glycol (78%) and 1,4-butanediol (87%), respectively. Subsequently, the linear curves were constructed between signal intensities of depolymerization products and polymer masses by GC-MS/MS, and the correlation coefficients of PET and PBT were 0.996 and 0.997, respectively. The spiking and recovery experiments of PET and PBT in the environmental samples showed that the recovery was stable in the range 89-100%, and the limit of detection was 4.95 µg and 1.39 µg of PET and PBT, respectively. The method has been proven to be capable of simultaneous identification and quantification of PBT and PET MPs in real environmental water samples without complex separation process, which provided a scheme for the determination of microplastics.

A Stable and Sensitive Engineering Bacterial Sensor via Physical Biocontainment and Two-Stage Signal Amplification.

Although engineering bacterial sensors have outstanding advantages in reflecting the actual bioavailability and continuous monitoring of pollutants, the potential escape risk of engineering microorganisms and lower detection sensitivity have always been one of the biggest challenges limiting their wider application. In this study, a core-shell hydrogel bead with functionalized silica as the core and alginate-polyacrylamide as the shell have been developed not only to realize zero escape of engineered bacteria but also to maintain cell activity in harsh environments, such as extremely acidic/alkaline pH, high salt concentration, and strong pressure. Particularly, after combining the selective preconcentration toward pollutants by functionalized core and the positive feedback signal amplification of engineering bacteria, biosensors have realized two-stage signal amplification, significantly improving the detection sensitivity and reducing the detection limit. In addition, this strategy was actually applied to the detection of As(III) and As(V) coexisting in environmental samples, and the detection sensitivity was increased by 3.23 and 4.39 times compared to sensors without signal amplification strategy, respectively, and the detection limits were as low as 0.39 and 0.86 ppb, respectively.

Simultaneous detection of As(III/V), Cr(III/VI), and Fe(II/III) by a sensor array based on the morphology regulation of CeO2 oxidase.

To develop a convenient method for simultaneous detection of As(III/V), Cr(III/VI), and Fe(II/III), three morphologies of CeO2 oxidase have been prepared. Based on the difference in oxidase activity and binding ability with substrate TMB of CeO2 of different morphologies, a 3 (Signal unit) × 6 (Target number) × 5 (Repetition) sensor array was constructed to realize simultaneous detection of six variable valence metal ions As(III/V), Cr(III/VI), and Fe(II/III). The lowest detection limit of the array for metal ions was 1.68 µg/L. The analysis of environmental samples with multiple metal ions (binary and ternary mixtures) co-existing has confirmed that the sensor array can achieve simultaneous qualitative and quantitative results for composite samples. This study not only revealed the influencing factors of crystal morphology regulation on oxidase activity, but also provided a scheme for the morphology detection of easily convertible metal ions in the field through the construction of the sensor array.

Enhancement of the Peroxidase Activity of g-C3N4 with Different Morphologies for Simultaneous Detection of Multiple Antibiotics.

The classes and forms of antibiotics directly determine their ecotoxicity and environmental chemical behavior, and developing a sensor array for simultaneous and in situ detection of antibiotics is highly anticipated. In this study, different morphologies of g-C3N4 with different fluorescence properties and peroxidase activity were prepared by regulating the degree of interlayer stacking and planar connectivity. Subsequently, in order to enhance its enzyme activity and amplify the differences in response signals to different antibiotics, three morphologies of g-C3N4/MIL-101(Fe) were prepared by in situ growth of equivalent amounts of MIL-101(Fe) on g-C3N4, respectively. The sensor array constructed based on the cross-response signals between g-C3N4/MIL-101(Fe) and antibiotics not only realized the simultaneous detection of quinolones, furans, tetracyclines, and lincomamides but also could efficiently identify their seven different forms. In the range of 0.2-0.8 ppm, the minimum detection limit for antibiotics was 12 ppb. In addition, the recovery experiments of multicomponent-mixed antibiotics in environmental samples show that the recovery rate remained at 91.42-107.59%, confirming the reliability and practicality of the sensor array. This study not only revealed the influence of crystal morphology regulation on the optical properties and enzyme activities of nanozymes, but also provided support for tracing, ecological remediation, and in situ environmental chemical behavior research of antibiotics.

Simultaneous visual detection of multiple heavy metal ions by a high-throughput fluorescent probe.

To develop simultaneous and in-situ detection techniques towards Cr(VI) and Mn(II), Eu/Tb@CDs with white fluorescence were prepared by a one-step hydrothermal method. With the increase of Cr(VI), all fluorescence channels of Eu/Tb@CDs exhibited obvious quenching, and the detection limit (LOD) was 0.10 µM. In the presence of Mn(II), only the fluorescence from Tb and Eu was quenched, while the fluorescence of CDs was not effected. The LOD for Mn(II) was 0.16 µM. More importantly, in the actual water samples where Cr(VI) and Mn(II) coexist, Eu/Tb@CDs can realize their rapid and simultaneous detection by simple spectral calculation. The selective and competitive experiments have also confirmed that the detection of Cr(VI) and Mn(II) was not interfered by common pollutants in groundwater. It is undeniable that the simultaneous detection of multiple targets by one probe not only greatly improves the detection efficiency, but also has important significance for the field monitoring of water quality parameters.

A portable and intelligent logic detector for simultaneous and in-situ detection of Al3+ and fluoride in groundwater.

To develop a convenient and intelligent detector for simultaneous and in-situ detection of Al3+ and F- in groundwater, a novel organic probe called RBP has been prepared. With the increase of Al3+, RBP showed a significant fluorescence enhancement at 588 nm, and the detection limit was 0.130 mg/L. After combining with fluorescent internal standard CDs, the fluorescence of RBP-Al-CDs at 588 nm was quenched due to the replace of F- for Al3+, while the CDs at 460 nm remained unchanged, and the detection limit was 0.0186 mg/L. For convenient and intelligent detection, an RBP-based logic detector has been developed for simultaneous detection of Al3+ and F-. Within the ultra-trace, low concentration, and high concentration range of Al3+ and F-, the logic detector can achieve rapid feedback on their concentration levels ("U", "L" and "H") through different output modes of the signal lamps. The development of logical detector is of great significance for studying the in-situ chemical behavior of Al3+ and F- and for daily household detection.

Ultra-trace detection and efficient adsorption removal of multiple water-soluble volatile organic compounds by fluorescent sensor array.

Due to the extremely low concentration, complex composition and easy to be converted into each other in water and air of water-soluble volatile organic compounds (VOCs), it is a great challenge to the traditional detection technology, pollution control and traceability, etc. Therefore, developing a convenient, swift and on-site detection method for simultaneous quantification of multiple VOCs is highly anticipated. In this paper, a multifunctional sensor array with adsorption and sensing of VOCs has been constructed by four fluorescence channels of small-sized Eu@Uio-66 and Tb@Uio-66. Due to the obvious cross-reactive characteristics between 4 fluorescence channels and VOCs, the sensor array could detect 8 VOCs simultaneously with all detection limits as low as ppb level. In addition, the detection results of sensor array for actual water samples coexisting with multiple VOCs confirmed that it has strong anti-interference performance and could be used for simultaneous detection of multiple VOCs in real water. The construction of sensor array with VOC adsorption function not only helps to reduce the detection limit of VOCs benefiting from the pre-concentration of materials, but also has significant value to reduce the harmfulness of pollutants. Predictably, this work is of great significance for VOC traceability, analysis of ecotoxicological effects and monitoring of pollution distribution characteristics.

New method for morphological identification and simultaneous quantification of multiple tetracyclines by a white fluorescent probe.

The threat of tetracycline antibiotics to the environment and human health is attracting widespread attention. The development of morphological analysis and quantitative techniques of multiple tetracyclines is of great significance for the evaluation of biochemical toxicity, wide-spectrum antibacterial property and degradation cycle between different tetracyclines. In this study, the white fluorescent Eu/Tb@CDs was synthesized and applied successfully to the identification and detection of the most widely used tetracycline antibiotics (tetracycline (TC), oxytetracycline (OC), chlortetracycline (CC) and doxycycline (DC)) with detection limits all below 1 nM. For the actual water samples with coexistence of the above 4 tetracyclines, their simultaneous morphology identification and accurate quantitative detection can also be realized through simple spectrometric measurement. In addition, the selective and competitive experiments have been carried out on the pollutants widely present in water, and the results have also confirmed that other pollutants could not interfere with the detection of the above 4 tetracyclines. It is undeniable that this work will conveniently and visually reveal the existence information and geographical distribution characteristics of different tetracycline antibiotics in the environment and their action mechanism on organisms.

Film-based fluorescent sensor for visual monitoring and efficient removal of aniline in solutions and gas phase.

Aniline has attracted much concern for its long degradation half-life and huge toxicity to the environment and human beings. Therefore, the development of a multi-functional device for visual detection and efficient removal of aniline was highly anticipated. In our work, the small-size Eu@UiO-66(COOH) was obtained by post-synthesis modification (PSM), and then the film-based fluorescent sensor was prepared by crosslinking reaction. The films not only showed incredible mechanical stability and potential for large-scale preparation, but also have excellent fluorescence response to aniline in solutions and gas phase. As the concentration of aniline increased, the fluorescence of films gradually increased at 350 nm, while the fluorescence gradually quenching at 620 nm, and the detection limits (LOD) of aniline in water and air were 0.27 ppb and 0.086 ppb, respectively. In addition, the adsorption performance of the film for aniline has also been confirmed and the maximum adsorption capacity was 32.6 mg/g, which is a strong guarantee for the realization of ultra-trace detection and toxicity reduction of aniline. In summary, the multi-functional film sensor has been designed for ultra-trace detection and efficient removal of aniline in solutions and gas phase, and have significant value for pollutant treatment, ecological restoration and early prevention.

Smartphone as a simple device for visual and on-site detection of fluoride in groundwater.

Developing a portable device for visual and on-site detection of fluoride in groundwater is highly anticipated. In this paper, 2-(tert-butyl-diphenylsilanyloxy)-5-nitro-1H-benzoimidazole (1) has been rationally designed via a silanization reaction for self-calibration detection of fluoride, and the detection limit was calculated as 0.11 µM. The contact of 1 with fluoride would induce the cleavage of Si-O bond and trigger the emergence of excited state intramolecular proton transfer (ESIPT) process, and then the enol-like emission at 437 nm decreased accompanying with the increase of keto-like tautomerism emission at 550 nm. More importantly, considering the demand of field detection for fluoride in groundwater and combining the function of smartphone to obtain the chroma of photos. The chroma value of the fluorescence color changes from blue to yellow could be conveniently determined through a color recognizer application installed in smartphone. The device can accurately reflect the concentration of fluoride by analyzing the chroma value. The test in actual water samples confirmed that the simple device based on smartphone could be used efficiently for visual, on-site and accurate detection of fluoride in groundwater.

A versatile logic detector and fluorescent film based on Eu-based MOF for swift detection of formaldehyde in solutions and gas phase.

Due to the huge threat of formaldehyde (FA) on human beings, the development of chemical sensors for swift detection of FA in solutions and gas phase is highly anticipated. In this paper, a versatile logic detector and a portable fluorescent film based on small-scaled Eu-based MOF were applied successfully to detect FA in solutions and gas phase, respectively. For FA in aqueous solution, the design of logic detector will efficiently identify FA in different concentration ranges: when the FA concentration are 0-500 ppb, 500-1000 ppb and >1000 ppb, the output signals of logic detector are the concentration level of FA ("L", "H" and "VH"), and accompanied by red, purple and blue signal lamps to remind, respectively. For FA in the air, the color of rigid film sensor will gradually change from red to blue with the increase of FA under UV lamp, and the detection limit of gaseous FA is 11.8 ppb. Through the preparation of logic devices and fluorescent films, Eu-based MOF realized swift detection of FA in solutions and gas phase, which will be very helpful to improve the human response level to FA from different emission sources.