Effective liquid–liquid extraction method for analysis of pyrethroid and phenylpyrazole pesticides in emulsion-prone surface water samples

Abstract Background Pesticide residue contamination of surface water in agricultural areas can have adverse effects on the ecosystem. We have performed an integrated chemical and bioanalytical profiling of surface water samples from Swedish agricultural areas, aiming to assess toxic activity due to presence of pesticides. A total of 157 water samples were collected from six geographical sites with extensive agricultural activity. The samples were chemically analyzed for 129 commonly used pesticides and transformation products. Furthermore, the toxicity was investigated using in vitro bioassays in the water samples following liquid–liquid extraction. Endpoints included oxidative stress response (Nrf2 activity), estrogen receptor (ER) activity, and aryl hydrocarbon receptor (AhR) activity. The bioassays were performed with a final enrichment factor of 5 for the water samples. All bioassays were conducted at non-cytotoxic conditions. Results A total of 51 pesticides and transformation products were detected in the water samples. Most of the compounds were herbicides, followed by fungicides, insecticides and transformation products. The highest total pesticide concentration in an individual sample was 39 µg/L, and the highest median total concentration at a sample site was 1.1 µg/L. The largest number of pesticides was 31 in a single sample. We found that 3% of the water samples induced oxidative stress response, 23% of the samples activated the estrogen receptor, and 77% of the samples activated the aryl hydrocarbon receptor. Using Spearman correlation coefficients, a statistically significant correlation was observed between AhR and ER activities, and AhR activity was strongly correlated with oxidative stress in samples with a high AhR activity. Statistically significant relationships were observed between bioactivities and individual pesticides, although the relationships are probably not causal, due to the low concentrations of pesticides. Co-occurrence of non-identified chemical pollutants and naturally occurring toxic compounds may be responsible for the induced bioactivities. Conclusions This study demonstrated that integrated chemical analysis and bioanalysis can be performed in water samples following liquid/liquid extraction with a final enrichment factor of 5. AhR and ER activities were induced in water samples from agricultural areas. The activities were presumably not caused by the occurrence of pesticides, but induced by other anthropogenic and natural chemicals.

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Determination of Parabens from Water Samples Using Cloud Point Extraction, Vortex Extraction and Liquid–Liquid Extraction Method Coupled with High Performance Liquid Chromatography

Journal of Computational and Theoretical Nanoscience ◽

10.1166/jctn.2020.8717 ◽

2020 ◽

Vol 17 (2) ◽

pp. 765-772

Author(s):

Noorashikin Md Saleh ◽

N. M. Hafiz ◽

Nik Nur Atiqah NikWee

Keyword(s):

Cloud Point ◽

Water Samples ◽

Extraction Method ◽

Optimum Parameter ◽

Cloud Point Extraction ◽

Liquid Extraction ◽

Extraction Time ◽

Solvent Ratio ◽

Liquid Liquid Extraction ◽

Method Of Extraction

A straightforward and efficient way for extraction of parabens that is methylparaben, ethylparaben, propylparaben and benzylparaben in environmental water samples was developed through optimizing parameters for each method of extraction. In this study, methods involved were cloud point extraction, vortex extraction, and liquid–liquid extraction. The parameters affecting the method of extraction were such as salt concentration, surfactant concentration, type of solvent, temperature, ratio of solvent to water and extraction time. The optimum parameter for cloud point extraction method were 1.0 M of salt, 1.0% v/v of surfactant, ratio of surfactant to water is 1:1, extraction time is 1 minute at 30 °C while vortex extraction method, optimum parameter is 1.0 M salt, using acetonitrile as a solvent, ratio 1 solvent: 4 water, and extracted at 1 minute. For the liquid–liquid extraction method, the optimum parameter was at 1.0 M salt, acetonitrile as a solvent, ratio of solvent to water is 1:1 and extraction time at 1 minute. The correlation coefficient for the calibration of paraben at concentration 0.2 ppm–1.0 ppm was in the range from 0.9703 to 0.9942. The limit of detection of studied paraben were 0.1627, 0.0837, 0.1156 and 0.1918 ppm, respectively. Percentage recovery for cloud point extraction, vortex extraction and liquid–liquid extraction were between 41%–147.9%, 26.5%–134.7%, and 31.4%–142.4% respectively. Each sample is repeated with triplication which the value of the relative standard deviation is less than 17.9%. Thus, the most suitable, efficient and effective method in extraction of paraben from water samples is cloud point extraction. The cloud point extraction shows the potential to be explore on the future extraction of others organic pollutants from water samples.

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Phytoremediation, Vermiremediation and Efficiency Assessments of Total Petroleum Hydrocarbons in Contaminated Surface Water from Okpoka Creek, Niger-Delta Nigeria using Cyperus odoratus, Colocasia esculenta, Phoenix roebelenii and Eisenia fetida

Journal of Advances in Biology & Biotechnology ◽

10.9734/jabb/2020/v23i830169 ◽

2020 ◽

pp. 1-12

Author(s):

C. Fawole ◽

S. J. Salami ◽

D. A. Dashak ◽

A. C. Harmony

Keyword(s):

Surface Water ◽

Petroleum Hydrocarbons ◽

Niger Delta ◽

Standard Procedure ◽

Liquid Extraction ◽

Total Petroleum Hydrocarbons ◽

Gas Chromatograph ◽

Liquid Liquid Extraction ◽

Us Epa ◽

Surface Water Samples

The liquid-liquid extraction of Petroleum contaminated surface water samples were conducted in accordance with standard procedure of US EPA. Identification and quantification of TPHs was performed by Gas chromatograph with Mass spectrometric detection (GC/MSD) in accordance with standard analytical method of US EPA 8270;625. The TPHs raw sample showed an elevated value of 104762.42 mg/L above the DPR/EGASPIN maximum contamination limit (MCL). At week 5, TPHs phytoremediations in the monoculture reactors removal efficiency was (31.28 mg/L) 99.97% and mixedculture indicated (19.72 mg/L) 99.98%; their concentrations were above DPR/EGASPIN MCL while polyculture indicated (8.91 mg/L) 99.99% value was below DPR/EGASPIN MCL. The combination of phytoremediation and vermiremediation techniques in polyculture reactors showed better and spectacular results as the biotas demonstrated good potentiality of hyperbioaccumulation to serve as hydrocarbon sinks from the ecotoxics of TPHs.

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Determination of tetraethyl lead in water samples by liquid-liquid extraction and gas chromatography / mass spectrometry

Modern Analytical Chemistry Research ◽

10.35534/macr.0201004c ◽

2020 ◽

Vol 2 (1) ◽

pp. 22-28

Author(s):

He Dingwen ◽

Mao Li

Keyword(s):

Mass Spectrometry ◽

Gas Chromatography ◽

Water Samples ◽

Liquid Extraction ◽

Gas Chromatography Mass Spectrometry ◽

Tetraethyl Lead ◽

Liquid Liquid Extraction ◽

Chromatography Mass Spectrometry

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Occurrence of 1,4-dioxane and MTBE in drinking water sources in Japan

Water Science & Technology Water Supply ◽

10.2166/ws.2006.049 ◽

2006 ◽

Vol 6 (2) ◽

pp. 47-53 ◽

Cited By ~ 5

Author(s):

D. Simazaki ◽

M. Asami ◽

T. Nishimura ◽

S. Kunikane ◽

T. Aizawa ◽

...

Keyword(s):

Drinking Water ◽

Surface Water ◽

Water Samples ◽

Quality Standards ◽

Raw Water ◽

Water Quality Standards ◽

Butyl Ether ◽

Water Treatment Plants ◽

Standard Value ◽

Surface Water Samples

Nationwide surveys of 1,4-dioxane and methyl-t-butyl ether (MTBE) levels in raw water used for the drinking water supply were conducted at 91 water treatment plants in Japan in 2001 and 2002, prior to the revision of the drinking water quality standards. 1,4-dioxane was widely and continuously detected in raw water samples and its occurrence was more frequent and its concentrations higher in groundwater than in surface water. However, its maximum concentration in raw water was much lower than its new standard value (50 μg/L), which was determined as a level of 10−5 excessive cancer risk to humans. Trace levels of MTBE were also detected in several surface water samples.

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Development of Surface Molecularly Imprinted Polymers as Dispersive Solid Phase Extraction Coupled with HPLC Method for the Removal and Detection of Griseofulvin in Surface Water

International Journal of Environmental Research and Public Health ◽

10.3390/ijerph17010134 ◽

2019 ◽

Vol 17 (1) ◽

pp. 134 ◽

Cited By ~ 1

Author(s):

Kamran Bashir ◽

Zhimin Luo ◽

Guoning Chen ◽

Hua Shu ◽

Xia Cui ◽

...

Keyword(s):

Surface Water ◽

Solid Phase Extraction ◽

Molecularly Imprinted Polymers ◽

Water Samples ◽

Solid Phase ◽

Phase Extraction ◽

Dispersive Solid Phase Extraction ◽

Molecularly Imprinted ◽

Imprinted Polymers ◽

Surface Water Samples

Griseofulvin (GSF) is clinically employed to treat fungal infections in humans and animals. GSF was detected in surface waters as a pharmaceutical pollutant. GSF detection as an anthropogenic pollutant is considered as a possible source of drug resistance and risk factor in ecosystem. To address this concern, a new extraction and enrichment method was developed. GSF-surface molecularly imprinted polymers (GSF-SMIPs) were prepared and applied as solid phase extraction (SPE) sorbent. A dispersive solid phase extraction (DSPE) method was designed and combined with HPLC for the analysis of GSF in surface water samples. The performance of GSF-SMIPs was assessed for its potential to remove GSF from water samples. The factors affecting the removal efficiency such as sample pH and ionic strength were investigated and optimized. The DSPE conditions such as the amount of GSF-SMIPs, the extraction time, the type and volume of desorption solvents were also optimized. The established method is linear over the range of 0.1–100 µg/mL. The limits of detection and quantification were 0.01 and 0.03 µg/mL respectively. Good recoveries (91.6–98.8%) were achieved after DSPE. The intra-day and inter-day relative standard deviations were 0.8 and 4.3% respectively. The SMIPs demonstrated good removal efficiency (91.6%) as compared to powder activated carbon (67.7%). Moreover, the SMIPs can be reused 10 times for water samples. This is an additional advantage over single-use activated carbon and other commercial sorbents. This study provides a specific and sensitive method for the selective extraction and detection of GSF in surface water samples.

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Homogeneous Liquid-Liquid Extraction Method for Selective Separation and Preconcentration of Trace Amounts of Palladium

E-Journal of Chemistry ◽

10.1155/2009/564276 ◽

2009 ◽

Vol 6 (4) ◽

pp. 1077-1084 ◽

Cited By ~ 5

Author(s):

Mohammad Reza Jamali ◽

Yaghoub Assadi ◽

Reyhaneh Rahnama Kozani ◽

Farzaneh Shemirani

Keyword(s):

Extraction Method ◽

Limit Of Detection ◽

Liquid Extraction ◽

Selective Separation ◽

Complexing Agent ◽

Homogeneous Liquid ◽

Liquid Liquid Extraction ◽

Relative Standard ◽

Separation And Preconcentration ◽

Ternary Component System

A simple and effective homogeneous liquid-liquid extraction method for selective separation, preconcentration and spectrophotometric determination of palladium(II) ion was developed by using a ternary component system (water / tetrabutylammonium ion (TBA+) / chloroform). The phase separation phenomenon occurred by an ion–pair formation of TBA+and perchlorate ion. Thio-Michler’s ketone (TMK), 4, 4ˊ-bis (dimethylamino) thiobenzophenone, was used as a complexing agent. After optimization of complexation and extraction conditions ([TMK]=5.0x10-2mol L-1, [TBA+] = 2.0×10-2mol L-1, [CHCl3] = 60.0 µL, [ClO4-] = 2.5×10-2mol L-1and pH= 3.0), a preconcentration factor 10 was obtained for 10 mL of sample. The analytical curve was linear in the range of 2-100 ng mL-1and the limit of detection was 0.4 ng mL-1. The relative standard deviation was 3.2% (n=10). Accuracy and application of the method was estimated by using test samples of natural and synthetic water spiked with different amounts of palladium(II) ion. The method is very simple and inexpensive.

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