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BACKGROUND: Carbon quantum dot (CQDs) are zero-dimensional carbon nanomaterials with a size of less than 10 nm CQDs are widely used in the field of ion detection by virtue of their fluorescence characteristics such as strong fluorescence intensity, good optical stability and tunable emission wavelength. Although the traditional atomic absorption method, electrochemical method and other metal ion detection methods are highly sensitive, the operation is complex, expensive and limited by the site. Therefore, we prepared the N, S-CQDs capable of detecting Hg2+ and MnO4- in water with the advantages of simple operation, low cost, and direct visual signal. RESULTS: N, S-CQDs with high-quantum yield (77.68%), uniform particle size (0.4 nm-2.6 nm) and green fluorescence were created utilizing a one-pot hydrothermal process with the precursors ASDA-Na4 and m-phenylenediamine. N, S-CQDs has good optical properties such as high fluorescence intensity, wavelength independence, up-conversion luminescence and fluorescence stability. We examined 27 common ions in water and found that the fluorescence of N, S-CQDs could be selectively quenched by Hg2+ and MnO4-, and the detection limits are 0.41 µM and 1.2 µM, respectively. The mechanism of quenching is further investigated. The fluorescence of N, S-CQDs-Hg2+ system can be restored by halogen ions (Cl-, Br-, I-), while the fluorescence of N, S-CQDs-MnO4- system can be partially restored by Fe2+. This forms an "on-off-on" mode of fluorescent probes. In addition, we also studied that trace amounts of N, S-CQDs can improve the photostability of RhB. SIGNIFICANCE: The N, S-CQDs are fluorescent probes in an "on-off-on" mode. N, S-CQDs with green fluorescence (on) can be quenched by Hg2+ and MnO4- (off). The fluorescence quenched by Hg2+ can be restored by halogen ions again, while the fluorescence quenched by MnO4- can partially be restored (on). This ion detection method can be used to visually detect the two ions in the field, with the advantages of low cost, simple operation and visual intuition.
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In this work, a fluorescent signal-closing probe of nitrogen-doped carbon quantum dots (NCQDs) was developed for quantitative detection of mercury ions (Hg2+). In this detection system, the NCQDs with high quantum yield (QY, 63.80 %) were synthesized via simple hydrothermal method with Methyl Glycine Diacetic acid Trisodium Salt (MGDA) and m-phenylenediamine (MPD) as carbon and nitrogen sources. The NCQDs have a typical surface structure and exceptional fluorescence stability, and their fluorescence zones are centered on excitation wavelengths of 440 nm and emission wavelengths of 510 nm. Under optimal conditions, the NCQDs have outstanding anti-interference ability to various ions and high selectivity to mercury ions. The fluorescence intensity of the detection system is weakened due to the generation of non-fluorescent groups caused by the static quenching effect. The fluorescence quenching efficiency shows a fascinating linear relationship with Hg2+ ions at 0-100 µM (y = 0.0051x-0.015, R2 = 0.9943), and the detection limit is 0.9 µM. Acute toxicity test shows that NCQDs have low toxicity and little harm to environment. The detection system can be used for the quantification of mercury ions in environmental water samples, and the recovery rate is between 99.64 % and 103.43 %, indicating that it is a simple and economical fluorescence detection method.
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Mercurio , Puntos Cuánticos , Puntos Cuánticos/química , Carbono/química , Nitrógeno/química , Agua , Espectrometría de Fluorescencia/métodos , Colorantes Fluorescentes/química , IonesRESUMEN
As an important environmental protection measure, the Poplar Ecological Retreat (PER) project aims to restore the ecology of the Dongting Lake (DL, China's second largest freshwater lake) wetland. And its ecological impact is yet to be revealed. This study selected soil bacterial community structure (BCS) as an indicator of ecological restoration to explore the ecological impact of PER project on DL wetland. Soil samples were collected from reed area (RA, where poplar had never been planted, as the end point of ecological restoration for comparison in this study), poplar planting area (PA), poplar retreat for 1-year area (PR1A) and poplar retreat for 2 years area (PR2A), then their soil properties and BCS were measured. The results showed that the PER project caused significant changes in soil properties, such as the soil organic matter (SOM) and moisture, and an increase in the diversity and richness index of soil BCS. The Shannon-wiener index of RA, PA, PR1A and PR2A were 3.3, 2.63, 2.75 and 2.87, respectively. The number of operational taxonomic units (OTUs) changed similarly to the Shannon-wiener index. The Pearson correlation analysis and redundancy analysis (RDA) showed that the poplar retreat time, SOM and moisture content were the main factors leading to the increase of BCS diversity. All of these indicated that after the implementation of the PER project, the ecology of the lake area showed a trend of gradual recovery.
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In this study, a novel ionic sensor based on nitrogen-doped carbon quantum dots (N-CQDs) was developed for sensitive detection of hypochlorite ions (ClO-) and dichromate ions (Cr(â ¥)) by fluorescence spectrometry. The N-CQDs was synthesized by hydrothermal method using Methyl Glycine Diacetic acid Trisodium Salt (MGDA) and Ethylenediamine (EDA) with bright blue fluorescence, high fluorescence quantum yield, abundant surface groups and good dispersion. The N-CQDs had a remarkable emission characteristic at 450 nm under the ultraviolet light of 350 nm, and the ClO- and Cr(â ¥) ions could quantificationally quench the fluorescence of this emission band. The results showed that N-CQDs had broad linear detection range and the detection limits of trace ClO- and Cr(â ¥) ions are 5.0 µM and 2.1 µM, respectively. Subsequently, further verify the reliability of this study and the N-CQDs played an excellent role in the ion detection of actual water samples. The quenching mechanism of ClO- is proved to be dominated by static quenching, while the quenching mechanism of Cr(â ¥) is mainly due to inner filter effect. This study is envisioned to efficiently prepare N-CQDs with novel raw materials, provide enlightening insights for enriching the detection of various trace ions by CQDs, and open up a new way to use fluorescence characteristics for water detection.
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Puntos Cuánticos , Carbono , Quelantes , Cromo , Colorantes Fluorescentes , Nitrógeno , Reproducibilidad de los ResultadosRESUMEN
In industry, isothiazolinone (a mixture containing 5-chloro-2-methyl-4-isothiazolin-3-one (CMIT) and 2-methyl-4-isothiazolin-3-one (MIT), CMIT-MIT) as a non-oxidizing biocide is extensively used to control the growth of microorganisms in the circulating cooling water system, which potentially threatens the ecological environment and human health. In this work, the oxidative degradation of CMIT-MIT by UV/persulfate (PS) technology on a laboratory-scale was systematically investigated. The degradation of CMIT-MIT was greatly improved by UV/PS compared with only UV or oxidant. During the photolysis of 60 mg/L PS, the degradation rate and TOC mineralization rate of CMIT-MIT were 91% and 34.7%, respectively. The contributions of .OH and SO4·- to CMIT-MIT degradation in the UV/PS system were estimated to be 0.93% and 32.12% respectively. The degradation rate of CMIT-MIT decreased slightly with the increase of pH. The presence of SO42- and NO3- had no significant effect on the degradation of CMIT-MIT, while the presence of Cl- and CO32- inhibited the CMIT-MIT removal rate. The degradation pathways and three possible intermediates of CMIT-MIT were obtained. After degradation of CMIT-MIT by UV/PS process, the cytotoxicity decreased within 20 min, effectively indicating that UV/PS could be as a potential technology to remove the CMIT-MIT in water treatment.
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Desinfectantes , Contaminantes Químicos del Agua , Purificación del Agua , Desinfectantes/toxicidad , Humanos , Cinética , Oxidación-Reducción , Fotólisis , Sulfatos , Rayos Ultravioleta , Contaminantes Químicos del Agua/análisis , Contaminantes Químicos del Agua/toxicidadRESUMEN
The 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt (PTSA) is a pyrene derivative with high fluorescence characteristics and is widely used in fluorescence tracer. This study aims at investigating a simple and fast fluorescence detection method for determining the concentration of ferric ion by using PTSA, which the principle is that the fluorescence quenching of PTSA by ferric ions. Theoretical and experimental methods were adopted to deeply analyze its detection performance and characteristics. The fluorescence quenching phenomena under different pH conditions and the effect of the different interfering metal ions on PTSA/Fe3+ system was studied. The results showed that the PTSA was quite promising for the fluorescence detection of trace ferric ions, and the limit of detection is 9 µg/L. This study is envisioned to provide inspirational insights on trace detection of iron ions, opening new routes for water monitoring use fluorescence properties.
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Bisulfite-activated permanganate (PM/BS) oxidation process can oxidize ciprofloxacin in complex water matrices rapidly. However, effects of PM/BS pre-oxidation on the formation of disinfection byproducts (DBPs) during post-chlorination of ciprofloxacin-contaminated waters need to be addressed. This study investigated the formation of trihalomethanes (THMs), haloacetonitriles (HANs), haloketones and trichloronitromethane during chlorination of ciprofloxacin-contaminated humic acid (HA), bovine serum albumin (BSA) and alginate solutions, and revealed the effects of PM/BS pre-oxidation on ciprofloxacin degradation and DBP formation during post-chlorination, considering the presence of Br-. Only THMs and HANs were quantifiable. THMs were the most abundant. Ciprofloxacin-contaminated HA exhibited the highest formation potential of DBPs and integrated toxic risk value (ITRV). In the absence of Br-, PM/BS pre-oxidation reduced or hardly affected the toxicity risks derived from DBPs formed from the post-chlorination. However, the presence of Br- greatly reduced the degradation of ciprofloxacin (30-50%) in various waters. In the ciprofloxacin-contaminated waters containing Br-, the total ITRVs of DBPs formed from post-chlorination increased by 60%-800% with PM/BS pre-oxidation, attributing to the enhanced formation of DBPs especially bromochloroacetonitrile and dibromoacetonitrile. Overall, PM/BS is a potential pre-oxidation technology for the treatment of ciprofloxacin-contaminated waters without bromide.