Journal of Analytical Methods in Chemistry
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2022
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IF 2.594
Zhen Pan,Xiaozhan Nong,Yajing Xie,Yan Li,Hui Zeng,Ying Liang,Min Zhang
Phosphate concentration in natural water has been used as a water quality indicator, as it is one of the major nutrients for aquatic plants. However, the traditional phosphomolybdenum blue (PMB) method has limited sensitivity for visual or camera-based detection, leading to underestimation of the phosphate concentration. We present an ultralow-cost, rapid field preconcentration and digital image colorimetric sensing of low-concentration phosphate method for water analysis. A novel hand-powered paper centrifuge (paperfuge) is used for sample preparation and preconcentration. This paperfuge is made of two circular paper discs and a string. Six centrifuge tubes (CTs) originally used as glue dispensing tips with a sample capacity of ∼230 μL, are loaded on the paperfuge. After sampling, phosphate in the water sample is reacted to form PMB. Then, the reacted sample is drawn into a CT using an autopipette before the CT bottom is sealed by glue. After Oasis® HLB sorbents are added through the top of the CT, the CT top is also sealed with glue. The HLB sorbents adsorb PMB and are accumulated in the CT tip through centrifugation. The CT tips are cut and analyzed with the ImageJ software. It was found that the blue color intensity of sorbents is in a linear relationship to the phosphate concentration, with a linear range of 0–5 μM (r2 = 0.9921) and limit of detection of 0.19 μM. In addition, this method has been applied to in-field water analysis. The results are in agreement with the standard PMB method.
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
ANALYTICAL CHEMISTRY
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2015
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IF 5.636
Anbang Zhu,Baiyang Chen,Liang Zhang,Paul Westerhoff
This study evaluated electrodialysis (ED) for direct, accurate, and precise dissolved organic nitrogen (DON) analysis in water. Unlike conventional methods that calculate DON as the difference between total dissolved nitrogen (TDN) and dissolved inorganic nitrogen (DIN), we designed a compact ED reactor as a pretreatment tool that completely separates DIN from DON in water and then measures DON by equating DON to TDN. The experiments confirmed that the ED pretreatment process can achieve 99% removal of all three major DIN species (i.e., ammonia, nitrite, and nitrate) and an average recovery rate of 88% for an array of model DON compounds of varying characteristics (e.g., urea, amino acids, tripeptide, protein, and humic substances). Variations in nitrogen removal and recovery might be explained by a combined effect of molecular weight, acid dissociation ability (pKa), aromaticity, and ED reactor configurations. For model solutions with DIN/DON ratios varying from 1 to 10 mg-N/mg-N, the relative standard deviations in DON concentrations were considerably lower with ED pretreatment (<10%) than without pretreatment (47%). A survey of seven field samples, including lake water, tap water, and treated wastewater, also demonstrated the benefits of using ED pretreatment as compared with a conventional DON analysis method. Overall, this study provides evidence and mechanistic insight for a new DON detection method that uses ED pretreatment. The ED unit is robust for separating DIN and DON, and thus it may facilitate more frequent detection of DON and ultimately enhances understanding of DON issues in the environmental studies.
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
TALANTA
·
2024
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IF 5.6
Kai Zhang,Yule Qian,Chaoyan Lou,Mingli Ye,Yan Zhu
PyICLab is an open-source Python-based package featuring an object-oriented programming (OOP) interface, providing tools for realistic and customized numerical simulations of ion chromatography (IC). In this paper, we showcase PyICLab's use in simulating diverse separation scenarios, including isocratic carbonate elution, gradient hydroxide elution, high-concentration and large-volume injections. The accuracy of the embedded models was validated by demonstrating strong correlations between predicted and experimental results. Additionally, PyICLab's capability to handle complex IC configurations was demonstrated through a simulation of a column-switching system for seawater analysis. PyICLab offers valuable resources for chromatographic optimization, method development, and educational purposes. It is available on PyPI at pypi.org/project/pyIClab. Interested readers can install PyICLab using the pip command in a Python 3.11 or higher environment.
研究领域:
分析化学
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计算科学
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PubMed
高影响因子
JOURNAL OF WATER AND HEALTH
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2025
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IF 2.4
Yuan Shuai,Xiao Yue,Luo Ruxin,Wang Xin,Xiang Ping
View large Download slide View large Download slide Close modal In recent years, mental disorders have become serious health problems. Monitoring the usage of psychotropic drugs can reflect the prevalence of mental disorders in the population, and wastewater analysis is an effective method for monitoring the use of psychoactive pharmaceuticals. In our study, we collected 58 samples from 12 wastewater treatment plants (WWTPs) in a southern city in China. We then analyzed the concentrations and loads of 18 frequently used psychoactive drugs and corresponding metabolites. The most abundant compounds in wastewater were diazepam, sulpiride, clozapine, venlafaxine, and quetiapine, with a detection frequency close to 100%. Sulpiride had the highest average load, followed by venlafaxine, clozapine, quetiapine, and diazepam. The higher load of diazepam in suburban WWTPs than in urban WWTPs reflects the large numbers of older people living in suburban areas in most of China. The lower loads of most target compounds in suburban WWTPs than in urban WWTPs indicate a greater likelihood of mental disorders in urban people than in suburban people. A correlation analysis of the target compounds revealed a correlation between the occurrence of venlafaxine, sulpiride, and clozapine. Overall, wastewater analysis is expected to be a significant tool for monitoring the consumption of psychoactive pharmaceuticals. Timing and regional distribution of 18 psychoactive drugs and metabolites in a Chinese city. The loads of most target compounds were lower in suburban WWTPs than in urban WWTPs. Schools showed high loads of diazepam, indicating that diazepam may be abused among students. Correlation was observed between venlafaxine, sulpiride, and clozapine loads.
研究领域:
环境科学
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公共卫生
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药理学
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产品关联
DOI
PubMed
高影响因子
ANALYTICAL CHEMISTRY
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2017
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IF 6.32
Mingrui Song,Junli Wang,Baiyang Chen,Lei Wang
Hydrogen peroxide (H2O2) is ubiquitous in the natural environment, and it is now widely used for pollutant control in water and wastewater treatment processes. However, current analytical methods for H2O2 inevitably require reactions between H2O2 and other reactants to yield signals and are thus likely subjective to the interferences of coexisting colored, oxidative, and reductive compounds. In order to overcome these barriers, we herein for the first time propose to analyze H2O2 by ion chromatography (IC) using an ultraviolet (UV) detector. The proposal is based on two principles: first, that H2O2 can deprotonate to hydroperoxyl ion (HO2–) when eluent pH is higher than the acid-dissociation coefficient of H2O2 (pKa = 11.6); and second, that after separation from other compounds via IC column, H2O2 can be quantified by a UV detector. Under favorable operating conditions, this method has successfully achieved acceptable recoveries (>91%) of H2O2 dosed to ultrapure and natural waters, a calibration curve with R2 > 0.99 for a wide range of H2O2 concentrations from 0.1 to 50 mg/L and a method detection limit of 0.027 mg/L. In addition, this approach was shown to be capable of distinguishing H2O2 from anions (e.g., fluoride and chloride) and organics (e.g., glycolate) and monochloramine, suggesting that it is insensitive to many neighboring compounds as long as they do not react quickly with H2O2. Hence, this study proves the combination of IC and UV detector a facile and reliable method for H2O2 measurement.
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
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART A-TOXIC/HAZARDOUS SUBSTANCES & ENVIRONMENTAL ENGINEERING
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2024
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IF 1.9
Yue Xiao,Shuai Yuan,Ruxin Luo,Yiling Tang,Xin Wang,Ping Xiang,Bin Di
The ketamine (KET) and its analogs consumed by humans are becoming emerging contaminants (ECs), as they at present in surface waters after being carried through wastewater systems. Drugs in wastewater can be analyzed using the direct-injection method, a simple wastewater analysis (WWA) method that can provide objective, continuous and nearly to real-time findings. This article describes an ultra-high-pressure liquid chromatography–tandem mass spectrometry (UPLC–MS/MS) method for the simultaneous quantification and confirmation of seven KET-based ECs in wastewater by direct injection. After optimization of the UPLC–MS/MS and sample pretreatment conditions, the method was validated and applied to samples (n = 157) collected from several wastewater treatment plants (WWTPs) in southern China in which KET had the highest detection rate. The established direct-injection method was not only simple to perform but also had better sensitivity, shorter detection times, and analyzed more KET-based ECs than currently published methods, meeting the requirements for the monitoring and high-throughput analysis of common KET-based ECs. We also analyzed the fragmentation pathway of KET-based ECs to obtain product ion information on other unknown substances. Additional studies are needed to establish a comprehensive direct-injection screening method of ECs in wastewater on model-based assessment.
研究领域:
环境科学
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分析化学
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毒理学
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DOI
PubMed
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2021
·Vol. 28
·期 20
·25503-25513
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IF 4.223
Cong Zi-Xiang,Shao Xue-Ting,Liu Si-Yu,Pei Wei,Wang De-Gao
Illicit drug use in rural and suburban areas of China has not been studied extensively, as most studies have focused on illicit drug use in urban areas. To compare the differences between urban, suburban, and rural drug use, we collected influent samples from 19 urban, 9 suburban, and 18 rural wastewater treatment plants in Dalian, respectively. A method using solid-phase extraction combined with derivatization for gas chromatography -mass spectrometry analysis was applied to detect biomarker concentrations. The concentrations of methamphetamine and morphine ranged from 3.12 to 605 ng/L and < 2.35 to 198 ng/L, respectively. Norketamine was found in only four samples (5.56 to 14.5 ng/L), while 3,4-methylenedioxymethamphetamine and benzoylecgonine were not detected in any samples. Methamphetamine use in rural areas (16.3 mg/day/1000 inhabitant (inh), prevalence: 0.06%) was significantly lower than those in urban (77.1 mg/day/1000 inh, prevalence: 0.23%) and suburban (234 mg/day/1000 inh, prevalence: 0.70%) areas. Heroin use in suburban areas (57.6 mg/day/1000 inh, prevalence: 0.10%) was significantly higher than that in urban (13.9 mg/day/1000 inh, prevalence: 0.02%) and rural (8.68 mg/day/1000 inh, prevalence: 0.02%) areas. The results indicate relatively low levels of illicit drug use in rural areas of Dalian, related to low incomes and outflow of the working-age population. Illicit drug use was most prevalent in suburban areas of Dalian, which may be influenced by large floating populations and few anti-drug efforts in suburban areas.
研究领域:
环境科学
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公共卫生
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毒理学
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2020
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IF 7.489
Yinming Fan,Guolong Zeng,Xiaoguo Ma
This work systematically investigated the effects of prepolymerization on the property of multi-templates surface molecularly imprinted polymer (MIP), which was utilized to quickly and simultaneously separate and detect six sulfonamides (sulfadiazine, sulfathiazole , sulfamerazine , sulfamethazine , sulfamethoxazole and sulfadoxine) in real waters. The MIPs were prepared using the six sulfonamides as the templates, mesoporous silica supported onto the surface of magnetic graphene oxide as the carrier and 4-vinylbenzoic as the functional monomer , with and without prepolymerization of templates with functional monomer. The preparation and adsorption conditions were optimized. It was found that the adsorption capacities of the selected six sulfonamides on the MIP (pre) prepared with prepolymerization were apparently higher than those on the MIP (no pre) synthesized without prepolymerization. Subsequently, the MIPs were utilized as adsorbents for SPE of these sulfonamides, and coupled with high performance liquid chromatography (HPLC) for the determination of sulfonamides. The developed analytical method showed outstanding applicability for the detection of trace sulfonamides in real water samples. The spiked recoveries and relative standard deviations (RSDs) of the six sulfonamides using MIP (no pre) and MIP (pre) were 73.34–99.43% and 87.37–102.34%, 2.28–7.77% and 3.18–6.49%, respectively.
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
Analytical Methods
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2023
·Vol. 15
·期 21
·2693-2699
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IF 3.1
Jianghua Chen,Yuanshuai Zang,Mengyi Chen,Chen Shi,Manlei Zhang,Bin Di,Cheng Jiang
As the dangers of cannabis abuse draw attention worldwide, it is necessary to assess the level of consumption in the community. The analysis of 11-nor-9-carboxy-Δ9-tetrahydrocannabinol (THC-COOH) excreted in wastewater can provide information for a defined catchment area. Due to its hydrophobic nature and absence of ionizable groups, its detection is challenging. In this study, a highly sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed for the quantitative determination of THC-COOH in urban wastewater. The derivatization reagent 6-methylpyridine-3-sulfonyl chloride (MPS) with analyte-specific fragmentation was proven to be the most effective for improving sensitivity. Samples were extracted by solid-phase extraction (SPE) and satisfactory recovery was achieved (>79%) by adding acetonitrile to the samples for ultrasonic-assisted extraction before filtration. The limit of detection (LOD) and limit of quantification (LOQ) was 0.03 ng L−1 and 0.1 ng L−1, respectively, from a 40 mL sample. The established methodology was applied to profile the presence of THC-COOH in influent wastewater samples. It was shown that 20 out of the 252 samples contained THC-COOH and the concentrations were all below 1 ng L−1.
研究领域:
环境科学
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分析化学
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毒理学
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产品关联
DOI
PubMed
高影响因子
TALANTA
·
2024
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IF 5.6
Junhui Xiao,Wen Yao,Dongxu Yan,Jie Yang,Ziyin Qiu,Lishi Wang,Xinrong Guo
In this study, a core-shell structural nano-composite material, namely CdTeS@SiO 2 , is synthesized by a simple silanization of Te-doped CdS quantum dots (CdTeS QDs). Through SiO 2 capping, CdTeS QDs not only improve the fluorescence performance effectively, but also greatly enhance the anti-interference ability in the environment. Based on its excellent optical properties , a novel fluorescence sensor is constructed for the ultramicro detection of Ag + . The fluorescence of CdTeS@SiO 2 is strongly quenched in the presence of Ag + and shows good linearity in the range of 0.005–5.0 μmol L −1 with a detection limit as low as 1.6 nmol L −1 . This is mainly due to its unique quenching mechanism: Ag + destroys the spherical structure of SiO 2 and promotes the formation of non-radiative electron-hole pairs through electron transfer , leading to fluorescence quenching . At the same time, it competes with Cd for Te, S and MPA on the CdTeS surface, forming Ag–Te, Ag–S and Ag–MPA complexes attached to the CdTeS surface leading to wavelength red-shift. The feasibility of the proposed sensor is demonstrated through spiking experiments, which confirmed the potential value of the constructed fluorescence probe for real-world applications in detecting Ag + in environmental water.
研究领域:
分析化学
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环境科学
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产品关联
DOI
PubMed
高影响因子
ANALYST
·
2015
·Vol. 140
·期 15
·5308-5316
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IF 4.107
Ting Wang,Jian Wang,Conglu Zhang,Zhao Yang,Xinpeng Dai,Maosheng Cheng,Xiaohong Hou
An attractive metal–organic framework (MOF) MIL-101(Cr) material was synthesized at the nanoscale and applied as a sorbent in the porous membrane-protected micro-solid-phase extraction (μ-SPE) device for the pre-concentration of phthalate esters (PAEs) in drinking water samples for the first time. Parameters influencing the extraction efficiency, such as the selection of sorbent materials, pH adjustment, the effect of salt, magnetic-stirring extraction time, the desorption solvent and the desorption time, were investigated. Under the optimum conditions, the limits of detection from gas chromatography-mass spectrometric analysis for PAEs varied from 0.004 to 0.02 μg L−1. The linear ranges were from 0.1 to 50 μg L−1 or from 0.2 to 50 μg L−1 for the analytes with the relative standard deviations fluctuating from 0.8 to 10.9% (n = 5). The enrichment factors (EFs) for the target PAEs were varied from 143 to 187. MIL-101(Cr) exhibited remarkable advantages compared to activated carbon and MIL-100(Fe). On the other hand, the computational method was first used to predict the adsorption of MIL-101(Cr) towards PAEs. The molecular interactions and the free binding energies between MIL-101(Cr) and PAEs were observed and calculated in terms of the molecular modeling method. MIL-101(Cr) showed high potential in the analysis of PAEs at trace levels in drinking water. The computational result was consistent with the detected enrichment factors. The computational modeling accurately predicted the extraction efficiency of MOF-based material towards the target analytes. Therefore, the combination of experimental and computational study provided a new strategy on the trace contaminant analysis.
研究领域:
分析化学
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材料科学
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环境科学
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产品关联
DOI
PubMed
高影响因子
MICROCHEMICAL JOURNAL
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2014
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IF 3.583
Shengling Sun,Jie Li
A method has been developed for the determination of zirconium (Zr), hafnium (Hf), niobium (Nb), tantalum (Ta), molybdenum (Mo), tungsten (W), and tin (Sn) in seawater by quadrupole inductively coupled plasma-mass spectrometry (Q-ICP-MS). The method is based on separation of the seven elements by extraction chromatography using N-benzoyl-N-phenylhydroxylamine (BPHA) supported on a microporous acrylic ester polymeric resin. The optimized procedure indicates that the BPHA resin has high selective adsorption for Zr, Nb, Mo, Sn, Hf, Ta, and W (known as fluoride soluble elements), whereas other interference and matrix elements are minimally adsorbed. The optimized eluent mixture with their molarity gives satisfactory recoveries for all analytes. The recovery can be achieved 99% for Zr, 97% for Nb, 97% for Mo, 99% for Sn, 99% for Hf, 95% for Ta, and 98% for W, respectively, by eluting with 6 mL of 6 mol L − 1 HF/1 mol L − 1 HCl. Furthermore, the technique for separation and enrichment of these elements provides a low total method blank. The detection limits for this method are 0.5 ppt for Zr, 0.2 ppt for Nb, 1.7 ppt for Mo, 1.0 ppt for Sn, 0.1 ppt for Hf, 0.1 ppt for Ta, and 0.3 ppt for W, respectively. The validity of the method is evaluated by replicate analyses of seawater reference materials; the precision of the results is better than 3% (RSD, n = 4), and the results are in good agreement with certified values. The established procedure has proved to be both practical and effective for seawater sample analyses.
研究领域:
分析化学
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海洋化学
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环境地球化学
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痕量元素检测
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质谱分析
✓ 已验证
DOI
高影响因子