scholarly journals Multi-residue analysis of polar pesticides in surface water and sediment by high performance liquid chromatography

2015 ◽  
Vol 18 (2) ◽  
pp. 159-165
Author(s):  
Hai Lam Son Truong ◽  
Trang Thi Thuy Nguyen ◽  
Huyen Ngoc Tran ◽  
Trang Thi Nhu Tran

We have successfully studied the analytical method of polar pesticides like carbofuran, pirimicarb, thiodicarb, atrazine, simazine, carbaryl, diuron, isoprocarb in surface water and sediment by HPLC-UV. The method could be applied to HPLC- MS. The stable recoveries ranged from 79 – 110 % with surface water and sediment samples. Especially, a cleanup procedure combined QuEChERS method and solid phase extraction has been developed to analyse these compounds in sediment, a very complex matrix.

2021 ◽  
Author(s):  
Stefan Krause ◽  

<p>It is probably hard to overestimate the significance of the River Ganges for its spiritual, cultural and religious importance. As the worlds’ most populated river basin and a major water resource for the 400 million people inhabiting its catchment, the Ganges represents one of the most complex and stressed river systems globally. This makes the understanding and management of its water quality an act of humanitarian and geopolitical relevance. Water quality along the Ganges is critically impacted by multiple stressors, including agricultural, industrial and domestic pollution inputs, a lack and failure of water and sanitation infrastructure, increasing water demands in areas of intense population growth and migration, as well as the severe implications of land use and climate change. Some aspects of water pollution are readily visualised as the river network evolves, whilst others contribute to an invisible water crisis (Worldbank, 2019) that affects the life and health of hundreds of millions of people.</p><p>We report the findings of a large collaborative study to monitor the evolution of water pollution along the 2500 km length of the Ganges river and its major tributaries that was carried out over a six-week period in Nov/Dec 2019 by three teams of more than 30 international researchers from 10 institutions. Surface water and sediment were sampled from more than 80 locations along the river and analysed for organic contaminants, nutrients, metals, pathogen indicators, microbial activity and diversity as well as microplastics, integrating in-situ fluorescence and UV absorbance optical sensor technologies with laboratory sample preparation and analyses. Water and sediment samples were analysed to identify the co-existence of pollution hotspots, quantify their spatial footprint and identify potential source areas, dilution, connectivity and thus, derive understanding of the interactions between proximal and distal of sources solute and particulate pollutants.</p><p>Our results reveal the co-existence of distinct pollution hotspots for several contaminants that can be linked to population density and land use in the proximity of sampling sites as well as the contributing catchment area. While some pollution hotspots were characterised by increased concentrations of most contaminant groups, several hotspots of specific pollutants (e.g., microplastics) were identified that could be linked to specific cultural and religious activities. Interestingly, the downstream footprint of specific pollution hotspots from contamination sources along the main stem of the Ganges or through major tributaries varied between contaminants, with generally no significant downstream accumulation emerging in water pollution levels, bearing significant implications for the spatial reach and legacy of pollution hotspots. Furthermore, the comparison of the downstream evolution of multi-pollution profiles between surface water and sediment samples support interpretations of the role of in-stream fate and transport processes in comparison to patterns of pollution source zone activations across the channel. In reporting the development of this multi-dimensional pollution dataset, we intend to stimulate a discussion on the usefulness of large river network surveys to better understand the relative contributions, footprints and impacts of variable pollution sources and how this information can be used for integrated approaches in water resources and pollution management.</p>


2008 ◽  
Vol 91 (6) ◽  
pp. 1459-1466 ◽  
Author(s):  
Ji-Ye Hu ◽  
Yu-Chao Zhang ◽  
Hai Yan

Abstract A method for high-performance liquid chromatographic (HPLC) determination of flumorph residues in cucumber, tomato, soil, and natural water was developed and validated. Primary secondary amine or octadecylsilyl (C18) solid-phase extraction cartridges were used for sample preparation. Reversed-phase HPLC with UV detection was used for separation and quantification of the pesticide. The combined cleanup and chromatographic method steps were sensitive and reliable for simultaneous determination of residues of the 2 isomers of flumorph in the studied samples. This method is characterized by recovery >97.9, coefficient of variation <6.2, and limit of quantification of 0.01 mg/kg, in agreement with directives for method validation in residue analysis. Flumorph residues in the samples were further confirmed by HPLC/mass spectrometry. The proposed method is fast, easy to perform, and could be used for monitoring of pesticide residues.


2019 ◽  
Vol 11 (27) ◽  
pp. 3460-3466 ◽  
Author(s):  
Qilin Deng ◽  
Liping Sun ◽  
Tao Zhu

In this study, a new and green fluorinated chitosan (trifluoroethyl methacrylate-chitosan (TFEMA-CTS)) was synthesized, and the QuEChERS method was applied for the effective determination of four pesticide residues in apple samples by high performance liquid chromatography.


2016 ◽  
Vol 99 (6) ◽  
pp. 1628-1635 ◽  
Author(s):  
Qianqian Sun ◽  
Yihu Wang ◽  
Chunxia Tian ◽  
Wenjun Gui ◽  
Yirong Guo ◽  
...  

Abstract A reliable and rapid method was developed to determine benzobicyclon residue in different soil and sediment samples. After extraction via a modified quick, easy, cheap, effective, rugged, and safe method, samples were purified by SPE cleanup with HLB cartridges. Quantitative determination was performed by ultra-HPLC (UPLC)-tandem MS (MS/MS) in electrospray positive ionization and multiple reaction monitoring modes. When samples were fortified at concentrations of 5, 50, and 500 µg/L, recoveries of 80.2 to 114.5% were obtained, with the repeatability (intraday RSDr) and reproducibility (interday RSDR) <14.1 and <21.4%, respectively. The instrumental LODs and LOQs for matrix-matched standards and the method LOQs for sample test were 0.19–1.34 μg/L, 0.64–4.48 μg/L, and 0.32–2.24 μg/kg, respectively. The linear range was 5–1000 μg/L (R2 > 0.99). The established UPLC-MS/MS method was applied in the detection of benzobicyclon in real soil samples, which were collected during the supervised field trial. Results showed that the maximum concentration of benzobicyclon in the soil was 4.87 mg/kg and its degradation half-life (t0.5) was 6.7 days. Generally, the proposed method could be an effective tool for controlling and monitoring the risks posed by benzobicyclon to human health and environmental safety.


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