JOURNAL OF MOLECULAR STRUCTURE
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2025
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IF 4.7
Luyue Wang,Yuzhu Chen,Zhengyang Xing,Jie Ma
Real-time monitoring of metal ion species and concentrations in water is a highly active research field. In the paper, a novel fluorescent molecule, (E)-N'-((5-(9-phenyl-9H-carbazol-3-yl) thiophen-2-yl) methylene) terephthalohydrazide (PCTMT), is synthesized via Suzuki reaction and Schiff-base reaction in turn. In the DMF-H 2 O (70 % v/v) solvent system, the PCTMT presents a good aggregation-induced enhancement (AIE) fluorescent effect and good selectivity and anti-interference for monitoring Co 2+ and Cu 2+ in water with a wide pH range. The probe's detection limit (LOD) reached 28.2 nM and 38.7 nM for Co 2+ and Cu 2+ , respectively. The binding constants between PCTMT and Co 2+ and Cu 2+ are calculated as 1.8 ×10 17 M -2 and 2.3 ×10 16 M -2 , at a 2:1 mol ratio. In the probe system, Co 2+ and Cu 2+ can be distinguished by oxalate titration. The detection mechanism is discussed through testing analyses with the theoretical simulation calculation via the density functional theory (DFT) and time-dependent density functional theory (TD-DFT). The probe also indicates good detection capacities in real water samples. This study may promote the development of coordinated-type ion probes and innovation in water quality detection technology.
研究领域:
分析化学
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环境科学
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DOI
高影响因子
MICROCHEMICAL JOURNAL
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2019
·
IF 3.206
Ya Dan Li,Hui Hui Chai,Shu Jie Zhang,Zhi Song Lu,Chang Ming Li,Ling Yu
A sensitive and portable on-thread pre-concentration and colorimetric detection method of copper ions was proposed. Commercial cotton thread was proposed as a solid sorbent for effectively extracting copper ions (Cu 2+ ) from solution. The adsorbed Cu 2+ was converted to Cu + by ascorbic acid . The Cu + on the threads was visualized by horseradish-peroxidase-catalyzed color changes of a chromogenic oxidized tetramethylbenzidine substrate. The adsorption of Cu 2+ on the plasma- and Na 2 CO 3 -treated thread was verified by scanning electron microscopy, energy-dispersive spectroscopy, X-ray diffraction, and zeta potential characterization. The Cu + -induced dysfunction of HRP on the thread was verified by X-ray photoelectron spectroscopy. With optimized reaction conditions, the concentration-dependent colorimetric response plot was characterized, where the linear detection range was 2–400 nM and the detection limit was about 0.15 nM. Measurements of a group of possible interfering ions and spiked real-water samples demonstrated the good selectivity of the proposed method. The proposed on-thread pre-concentration and colorimetric detection offers a low-cost and effective alternative for detecting of copper ions in real applications.
研究领域:
分析化学
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环境科学
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DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2023
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IF 7.7
Yixin Huang,Jing Zou,Jiawen Li,Hongfang Ma,Siying Chen,Lingying Chen,Xiaobin Liao,Jun Ma
In this study, a rapid, sensitive and reliable spectrophotometric method for peroxydisulfate (PDS) determination in water was established. The proposed spectrophotometric method was based on the oxidation of 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonate) (ABTS) to form stable and green-colored ABTS radical (ABTS • + ) by ferrous ion (Fe(II))-catalyzed PDS. The formed ABTS • + performed well linear relationship with PDS concentration (R 2 > 0.999) in the range of 0–60 μM at four wavelengths of 415, 650, 732, and 820 nm under optimized conditions. The proposed Fe(II)-ABTS spectrophotometric method was highly sensitive with the absorptivity of 3.595 × 10 4 M −1 cm −1 , 1.530 × 10 4 M −1 cm −1 , 1.945 × 10 4 M −1 cm −1 and 1.768 × 10 4 M −1 cm −1 at four detection peaks of 415, 650, 732 and 820 nm, respectively. Additionally, the proposed Fe(II)-ABTS spectrophotometric method possessed well anti-interference capacity to common natural water constituents and was reliable to determine PDS concentration in water. What’s more, the proposed Fe(II)-ABTS spectrophotometric method was successfully applied in monitoring the change of PDS concentration during the degradation of diclofenac in heat-activated PDS process. In a word, the proposed Fe(II)-ABTS spectrophotometric method could be employed as a promising approach for the rapid and accurate measurement of PDS in water, and this study provided a new perspective for the measurement of PDS by the visible spectrophotometry .
研究领域:
分析化学
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环境科学
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高影响因子
ANALYTICAL SCIENCES
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2019
·Vol. 35
·期 5
·551-556
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IF 1.618
Hongli YANG,Yongxin HUANG,Yanjun ZHAO,Aiping FAN
A simple and sensitive chemiluminescent (CL) sensing platform for mercury(II) ions (Hg2+) in water was developed based on monolayer molybdenum disulfide (MoS2). The layered MoS2 can catalyze the oxidation of luminol by H2O2, producing an enhanced CL signal because of the peroxidase-like activity of the layered MoS2. In addition, MoS2 has a good adsorption ability to Hg2+ because of the inherent affinity of Hg2+ to sulfur contained in MoS2. Interestingly, the pre-incubation of Hg2+ with layered MoS2 inhibited the catalytic activity of MoS2 on the luminol–H2O2–MoS2 CL reaction, leading to CL quenching. The CL intensity decreased linearly with increasing concentration of Hg2+ from 0.005 – 40 μM. The limit of detection (LOD) was estimated to be 1 nM. The relative standard deviation (RSD) was found to be 3.71%, indicating good reproducibility. The recoveries of Hg2+ spiked in tap water were from 100.0 to 116.0% with RSD from 2.7 to 5.6%, detected by the standard addition method, and demonstrated good applicability.
研究领域:
分析化学
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环境科学
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材料科学
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产品关联
DOI
PubMed
高影响因子
Environmental Science-Nano
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2025
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IF 5.1
Bingqian Jing,Yuanyuan Li,Xiaofeng Liu,Zihang Zeng,Zan Long,Bingni Jia,Bo Feng,Peng Zhang,Taiping Qing
The widespread use of triazine pesticides in agricultural practices raises concerns regarding their potential harm to both humans and the environment, given their known carcinogenic and neurotoxic effects. Triazine pesticides exhibit various toxic effects on organisms, posing a significant challenge in accurately distinguishing them due to their analogous structures. Herein, we functionalized platinum nanoparticles (Pt NPs) and constructed a three-channel sensing array by modulating their oxidase-like activities through various ligands on the surface of Pt NPs. Triazine pesticides can inhibit the activity of functionalized Pt NPs, allowing the substrate TMB to show different degrees of color development reaction, which provides a solid basis for the construction of sensing arrays by platinum nanozymes. The proposed platinum nanozyme sensing array showed good performance for the identification of five kinds of triazine pesticides (atrazine, simazine, metribuzin, metamitron, and terbutryn) across a wide range of concentrations (0.5-100 µg/mL) through statistical classification using advanced algorithms like linear discriminant analysis (LDA) and hierarchical cluster analysis (HCA). Importantly, the sensing array exhibited good anti-interference ability and achieved accurate discrimination of structurally similar triazine pesticides in real water samples. This study provided a simple and effective method for the identification of triazine pesticides, with potential for discriminating other related pollutants such as antibiotics and biotoxins for environmental monitoring and food safety.
研究领域:
环境科学
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分析化学
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生物医学工程
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DOI
高影响因子
TALANTA
·
2019
·
IF 4.916
Wenqiang Jing,Yanying Zhou,Jiaqin Wang,Yuanfeng Zhu,Youqi Lv,Wentao Bi,David Da Yong Chen
A sorbent and solvent co-enhanced direct analysis in real-time mass spectrometry (SSE-DART-MS) method was developed for high-throughput determination of trace pollutants in water. The use of sorbent for preconcentration and solvents for assisting desorption and ionization synergistically enhanced the signals from the trace pollutants detected by DART-MS. Phthalic acid esters (PAEs) were used as model analytes to validate the SSE-DART-MS method. Graphitic carbon nitride (g–C 3 N 4 )–based materials with two morphologies and six organic solvents were used to systematically evaluate the enhancement effect by the sorbent and solvent. A better analytical performance was achieved with the two-dimensional (2D) g-C 3 N 4, compared to three-dimensional (3D) g-C 3 N 4 /C, indicating that the morphologies of sorbents played a key role in SSE-DART-MS analysis. The MS signals of all the analytes were increased by 10–100 times for the two materials in the presence of the selected solvents. With the SSE-DART-MS method, concentration limits of detection for water samples in the range 0.07–0.94 ng L −1 , and recovery in the range 82.8–119% using g-C 3 N 4 , were obtained for the PAEs. This work not only provides a reliable method for the coupling of solid phase extraction technique with DART-MS, but also presents valuable information for conducting other DART-MS analyses.
研究领域:
环境科学
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分析化学
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DOI
PubMed
高影响因子
LUMINESCENCE
·
2021
·Vol. 37
·期 1
·72-81
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IF 2.464
Haonan Zhao,Junfeng Zhang,Xiaolian Lin,Huihui Li,Qinhe Pan
Cr(VI) is a type of dangerous effluent that has caused great harm to human health and the environment. Recognition and perception of Cr(VI) by artificial receptors has attracted extensive attention. A novel fluorescent chemical sensor based on the 5,7-dihydroxyflavone skeleton was designed and synthesized for the selective recognition of Cr(VI). As confirmed by fluorescence technology, the fluorescent probe 4-dimethylaminobenzyl chrysin ester–Zn (DBC–Zn) showed high sensitivity and selectivity for dichromate and a fast response (less than 30 sec) recognition. The fluorescence intensity of DBC–Zn varies linearly with the concentration of Cr(VI) in the range 0.1–1 μM. The detection limit of Cr 2 O 7 2− by DBC–Zn is 2.3 nM, which is far lower than the national safe drinking water standard stipulated by the US Environmental Protection Agency (1.9 μM). The quenching mechanism of the probe can be attributed to the interaction of the dynamic quenching effect and the fluorescence internal filtration effect. In addition, the probe has good stability in both neutral and alkaline environments, and the accuracy of quantitative analysis of Cr 2 O 7 2− in lake water or tap water is more than 80%. The test paper based on DBC–Zn can effectively detect Cr 2 O 7 2− at the concentration of 100 ppb. This shows that the probe has a certain practical application value.
研究领域:
环境科学
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分析化学
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产品关联
DOI
PubMed
高影响因子
Surfaces and Interfaces
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2025
·
IF 6.3
Fen Yang,Shuai Zhao,Biaobiao Ge,Jie Huang,Qianmin Dong,Qiang Chen,Shangzhong Jin,Pei Liang
We demonstrate a method for the detection of Ziram in water by using the adsorption properties of UiO-66(Ce) metal-organic framework (MOF) combined with the surface-enhanced Raman scattering (SERS) substrate of precious metal nanoparticles. The traditional UiO-66 is based on Zr as the metal center. After replacing the Zr metal center with Ce, the synthesized UiO-66(Ce) has short aging, high efficiency, low energy consumption, and energy saving. Furthermore, by adding P123, UiO-66 is modified to have a structure similar to the durian shell spine, which can provide more composite sites for metal nanoparticles. Thus, more SERS hot spots are generated. The combination of AuNPs with UiO-66(Ce) has been confirmed by XRD, XPS, and other characterization and analysis techniques. The Raman probe molecule R6G was used as an evaluation tool to evaluate the performance of this SERS substrate. The results showed that the relative standard deviation (RSD) of the substrate was as low as 8.96 % at a concentration of 10 –6 M of the R6G solution, and the substrate demonstrated high stability. Finally, the substrate was applied for the detection of ziram in lake water, achieving a detection concentration of 10 –8 M, an enhancement factor of 2.57 × 10 5 , and a detection limit as low as 5.21 × 10 –9 M, demonstrating excellent sensitivity and enabling efficient trace pollutant detection in complex water environments.
研究领域:
环境科学
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分析化学
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DOI
高影响因子
DYES AND PIGMENTS
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2020
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IF 4.613
He Li,Donglin Li,Bowen Qin,Wenliang Li,Haoyan Zheng,Xiaoying Zhang,Jingping Zhang
An extremely stable pillar-layered metal-organic framework (MOF), [Cd 4 (NDC) 3 (4-Hptz) 2 (H 2 O) 2 ]·H 2 O (1), has been successfully designed and synthesized (4-Hptz = 5-(4-pyridyl)-tetrazolate, NDC = 1,4-Naphthalenedicarboxylic acid). Compound 1 can detect Cr 3+ in water by fluorescence enhancement, which is the first known case of MOF. This is of great significance for our study on new fluorescent probes .
研究领域:
材料科学
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环境科学
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分析化学
✓ 已验证
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
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2014
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IF 4.331
Shian Zhong,Chengyun Zhou,Xiaona Zhang,Hui Zhou,Hui Li,Xiaohong Zhu,Yan Wang
A new type of magnetic halloysite nanotubes molecularly imprinted polymer (MHNTs@MIP) based on halloysite nanotubes (HNTs) with embedded magnetic nanoparticles was introduced in this study. MHNTs@MIP was prepared through surface imprinting technology, using 2,4-dichlorophenoxyacetic acid (2,4-D) as a template, 4-vinylpyridine as the monomer, divinylbenzene as cross-linking agents, and 2,2-azodiisobutyronitrile as initiator. MHNTs@MIP was characterized by Fourier Transform Infrared Spectrometer, transmission electron microscopy, X-ray diffraction, and vibrating sample magnetometer. MHNTs@MIP exhibited rapid and reliable analysis with supermagnetic properties, as well as repeated use and template-specific recognition. The adsorption capacity of magnetic halloysite nanotubes non-imprinted polymer (MHNTs@NIP) and MHNTs@MIP was 10.3 mg/g and 35.2 mg/g, respectively. In the detailed discussion on specific selectivity, MHNTs@MIP can be applied as an adsorbent for sample pretreatment extraction and obtain high recoveries of about 85–94%. After extraction, high-performance liquid chromatography was used to detect 2,4-D residue in water.
研究领域:
环境科学
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分析化学
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产品关联
DOI
PubMed
高影响因子
CHEMOSPHERE
·
2018
·
IF 4.427
Xin Liu,Huahua Cai,Jing Zou,Zijun Pang,Baoling Yuan,Zhenming Zhou,Qingfeng Cheng
A sensitive spectrophotometric method (the N,N -diethyl- p -phenylenediamine (DPD) method) was established for the determination of trace permanganate concentration (0–10 μM) in water. The DPD method was based on the oxidative coloration reaction where permanganate could oxidize DPD to form the red colored DPD radical (DPD • + ) with a second-order rate constant of 2.96 × 10 4 M −1 s −1 at pH 6 (50 mM phosphate buffer). The generated DPD • + could be quantitatively measured at 551 nm using an UV–Vis spectrophotometer. There was a good linear relationship (R 2 = 0.999) between the absorbance of DPD • + and permanganate concentration. The DPD method was highly sensitive, and the absorbance of generated DPD • + at 551 nm was as high as 5.70 × 10 4 cm −1 per M (mol L −1 ) of permanganate. The reaction of permanganate with DPD in the pH range of 4.0–8.0 had a stoichiometric coefficient of 1:2.71. The residual absorbance of DPD •+ in ultrapure water and natural waters was fairly stable for 30 min. Limits of detection of the proposed DPD method in ultrapure water and natural waters were calculated to be as low as 0.010 μM and 0.017 μM, respectively. Moreover, trace permanganate concentrations of 0.04 and 0.10 μM were found in natural waters and wastewater by the proposed DPD method. Additionally, the DPD method could be applied to measure the second-order rate constants of the reaction of permanganate with phenol at pH 7.0 (28.2 M −1 s −1 ).
研究领域:
分析化学
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环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ACS Applied Nano Materials
·
2021
·
IF 5.097
Yuhui Miao,Kuo Yang,Shenfei Zong,Zhuyuan Wang,Yiping Cui
Applying nanomaterials to highly sensitive, fast, and accurate detection of hazardous chemicals in water remains to be a great challenge. Herein, a Ti3C2-functionalized superlattice SERS substrate was developed, which can identify multiplex fish drug residues in pond water with a high sensitivity and reliable reproducibility. Specifically, a superlattice substrate was fabricated by vertically self-assembled bimetallic nanocuboids (BNCs) through the Marangoni effect, which exhibited an excellent SERS activity. Furthermore, the modification of the Ti3C2 layer endows the substrate with both an increased SERS signal and an enhanced adsorption for multiple fish drugs, including crystal violet (CV), malachite green (MG), and methylene blue (MB). The limit of detection (LOD) was as low as 10–12 M, while the signal fluctuation was as small as ∼5.9% between batches. More importantly, a trace amount of multiplex fish drug residues was detected in natural pond water, demonstrating a convincing practicality of such a Ti3C2-functionalized superlattice SERS substrate.
研究领域:
材料科学
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环境科学
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分析化学
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产品关联
DOI
高影响因子
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