On-site Water Monitoring Research Articles

Space-temporal analysis of groundwater quality in three areas of the state of Yucatán, México, and its relationship with existing anthropogenic activity.

Groundwater in the Yucatan State is the only source of water. The karst aquifer in Yucatan is vulnerable to pollution. Anthropic activities in Yucatan, such as pig farming, are usually related to high wastewater discharges and water pollution. Administrative and logistical issues in developing on-site sampling to evaluate water quality are common in Mexico. The RENAMECA database provides official data related to groundwater quality. However, no analysis based on this database has been reported. A groundwater quality evaluation based on five reference pig farms and the effect of spatial and temporal anthropic activities in the study area was developed. Eighteen wells based on their location concerning the selected pig farms were studied. On-site sampling and laboratory analysis of the supply water and wastewater in the study case farm were done. Fecal coliforms (FC) values (maximum 2850 MPN [100mL] -1) in most cases for supply water wells exceeded the allowed limit by NOM-127-SAA1-2021. The year of monitoring was significant (P < 0.05) on FC concentrations. Population density and the proximity of wells to population centers affect negatively the presence of total dissolved solids (TDS) and total nitrogen (TN). TDS (maximum value 2620mg L -1) and phosphorus presence could be related to agricultural activities, human settlements, and local aquifer conditions. A local wastewater treatment issue is evident. Groundwater is not quality for consumption without treatment. Regarding the issues in on-site water monitoring, database analysis provides an approximation of the real situation of groundwater quality.

An Electrochemical Sensor Based on Three-Dimensional Porous Reduced Graphene and Ion Imprinted Polymer for Trace Cadmium Determination in Water

Three-dimensional (3D) porous graphene-based materials have displayed attractive electrochemical catalysis and sensing performances, benefiting from their high porosity, large surface area, and excellent electrical conductivity. In this work, a novel electrochemical sensor based on 3D porous reduced graphene (3DPrGO) and ion-imprinted polymer (IIP) was developed for trace cadmium ion (Cd(II)) detection in water. The 3DPrGO was synthesized in situ at a glassy carbon electrode (GCE) surface using a polystyrene (PS) colloidal crystal template and the electrodeposition method. Then, IIP film was further modified on the 3DPrGO by electropolymerization to make it suitable for detecting Cd(II). Attributable to the abundant nanopores and good electron transport of the 3DPrGO, as well as the specific recognition for Cd(II) of IIP, a sensitive determination of trace Cd(II) at PoPD-IIP/3DPrGO/GCE was achieved. The proposed sensor exhibited comprehensive linear Cd(II) responses ranging from 1 to 100 μg/L (R2 = 99.7%). The limit of detection (LOD) was 0.11 μg/L, about 30 times lower than the drinking water standard set by the World Health Organization (WHO). Moreover, PoPD-IIP/3DPrGO/GCE was applied for the detection of Cd(II) in actual water samples. The satisfying recoveries (97–99.6%) and relative standard deviations (RSD, 3.5–5.7%) make the proposed sensor a promising candidate for rapid and on-site water monitoring.

Automated Drone-Delivery Solar-Driven Onsite Wastewater Smart Monitoring and Treatment System.

Treating potential polluted water sources is urgent and challenging, especially for natural water sources. Numerous research groups focus on either smart water monitoring or new adsorbent. However, either aspect alone is insufficient for complex nature water source treatment. Here, integrating the state-of-art machine learning technique, a sustainable silk-based bioadsorbent, and wireless Internet of Things, an integrated automated drone-delivery solar driven onsite water monitoring & treatment system (WMTS) for the contaminated nature water sources is developed. In short, the embedded sensors and microprogrammed control unit capture and upload the real-time monitoring data to the cloud server for data analysis and optimized treatment strategy. Meanwhile, a grid map system based on the satellite remote sensing images directs the minimum number of WMTS units to cover the entire polluted region. Finally, unmanned aerial vehicles provide autonomous dispatch, operation, and maintenance, especially in hard-to-reach sites. Overall, this work offers a general, sustainable, energy-efficient, and closed-loop solution toward efficiently alerting and on-site treating nature water source contamination.

Electrochemical detection of nitrate, nitrite and ammonium for on-site water quality monitoring

This review examines the most recent electrochemical developments for nitrate, nitrite and ammonium detection for on-site water monitoring. There remains a high demand for effective field-based detection of the dissolved inorganic nitrogen (DIN) analytes to aid in mitigating nitrogen loading. Electrochemical approaches show increasing potential to fill this role as advancements in nanotechnology continually improve analytical performance and on-site applicability. However, translating these improvements into the field still faces the resonating challenges of reaching analytical proficiency (selectivity, sensitivity, robustness, stability), practical end-user functionality, minimal matrix interferences and cost effectiveness. Herein, we elaborate on these challenges via a critical evaluation of current studies and examine how realistic the prospects of on-site nitrate, nitrite and ammonium are. We also present recommendations in addressing these gaps to conclude the review. • Recent developments for electrochemical detection of nitrate, nitrite and ammonium are discussed. • A critical examination of current nitrate, nitrite and ammonium studies as realistic monitoring processes is presented. • The functionality of such devices in remote locations are elucidated. • Recommendations for increased inorganic nitrogen monitoring in sensitive areas like the Great Barrier Reef.

Lead Assays with Smartphone Detection Using a Monolithic Rod with 4-(2-Pyridylazo) Resorcinol.

A monolithic rod of polyurethane foam–[4-(2-pyridylazo) resorcinol] (PUF–PAR) as a simple chemical sensor for lead assays with smartphone detection and image processing was developed. With readily available simple apparatus such as a plastic cup and a stirrer rod, the monolithic PUF rod was synthesized in a glass tube. The monolithic PUF–PAR rod could be directly loaded by standard/sample solution without sample preparation. A one-shot image in G/B value from a profile plot in ImageJ for a sample with triplicate results via a single standard calibration approach was obtained. A linear single standard calibration was: [G/B value] = −0.038[µg Pb2+] + 2.827, R2 = 0.95 for 10–30 µg Pb2+ with a limit of quantitation (LOQ) of 33 µg L−1. The precision was lower than 15% RSD. The proposed method was tested by an assay for Pb2+ contents in drinking water samples from Bangkok. The results obtained by the proposed method agree with those of ICP-OES and with 100–120% recovery, demonstrating that the method is useful for screening on-site water monitoring.

Ratiometric fluorescent probe for the on-site monitoring of coexisted Hg2+ and F− in sequence

The monitoring of mercury and fluoride ions (Hg2+ and F−) has aroused wide concerns owing to the high toxicity of Hg2+ and the duplicitous nature of F− to human health. As far as we known, more than 100 million people in poverty-stricken areas are still at high risk of being over-exposed to Hg2+ and F− via drinking water. Simple and cost-effective luminescent methods are highly promising for on-site water monitoring in rural areas. However, the development of multipurpose luminescent probes that are accurate and sensitive remains challenging. Herein, a new strategy for rationally designing a multipurpose ratiometric probe is present. The obtained probe is consisted of two emission units with energy transfer between them, which exhibit high coordination affinities to the two coexisted toxic targets (Hg2+ and F−), respectively. Thus, two distinct routes for efficiently modulating the energy transfer in the probe are present to trigger the responses to the two targets in sequence. By detecting the shift of the emission color with a smartphone, an on-site water monitoring method is successfully established with the detection limits as low as 2.7 nM for Hg2+ and 1.9 μM for F−. The present study can expend the toolbox for water monitoring in rural regions.

An electrophoretic ion analyzer for on-site autonomous water monitoring

An on-site ion analyzer based on capillary electrophoresis with pressure-driven flow through injection and capacitively coupled contactless conductivity detection has been developed for field monitoring of cations and anions in environmental waters. Automated time-pressure based hydrodynamic injection provides stable pL-nL scale injection (RSD = 1.96%, n = 30). A mixture of 400 mM Bis-Tris, 400 mM MOPS and 2 mM 18-crown-6 is used as the background electrolyte to provide repeatable separations. A proprietary hydrophilic coated 25 μm id capillary is used to suppress the electroosmotic flow. Separations of anions (Cl-, NO3-, NO2-, SO42-, F- and PO43-) and cations (NH4+, K+, Na+, Ca2+ and Mg2+) are achieved by switching the polarity of the high voltage power supply in two individual runs. Signal fluctuations caused by the temperature or viscosity changes in on-site monitoring are corrected by on-line introduction of internal standards. RSDs of the migration time and the corrected peak height over ~35 h and 350 analysis cycles are <4.06%. The LODs of inorganic ions are in the range of 2.1 μM (K+) to 6.8 μM (PO43-). The feasibility for on-site water monitoring with this system has been validated by a standard Ion chromatography method with comparable results obtained.

Optimization of innovative composite sensor for Pb(II) detection and capturing from water samples

In developing countries, the lack of analytical infrastructures hindering the regular quality assessments of water quality. The access to affordable, portable and easy-to-use analytical technologies for real-time and on-site water monitoring is necessary to safeguard public health and protect the environment. In this connection, ligand based composite sensor material was successfully developed for optical detection and removal of toxic lead (Pb(II)) ion from water. The fabricated sensor was exhibited the specific functionality for Pb(II) detection and removal from aqueous media in ultra-trace level. The Pb(II) ion detection limit was defined as low as 0.24 µg/L with evolving specific color formation at optimum conditions. The solution acidity was the key point for the formation of specific color after addition of Pb(II) ion by the sensor material. The effect of diverse competing ions were not significantly affected in the Pb(II) ion detection. Moreover, the Pb(II) ion removal data were well fitted to the Langmuir model and the maximum adsorption capacity was 155.27 mg/g. The prepared sensor was completely eluted with 0.20 M HCl after optimum Pb(II) adsorption and then simultaneously regenerated into the initial form for the next detection and removal operation after rinsing with water. The performance of the sensor material platform provides an alternative way to detect Pb(II) ion in trace level in real-life water samples. In addition, the methodology can lead to an affordable and portable diagnostic tool for rapid and on-site monitoring of heavy metals pollution in developing countries.

Engineering of a Au-sensor to develop a Hg-specific, sensitive and robust whole-cell biosensor for on-site water monitoring.

A highly sensitive and specific Hg-whole-cell biosensor was developed from a non-selective variant of the Au sensor GolS and its regulatory pathway. The performance of this analytical tool was validated under laboratory and field-like conditions. This biosensor can be easily applied in cost-effective and portable semiquantitative devices to report Hg contamination in water.

Rapid and on-site simultaneous electrochemical detection of copper, lead and mercury in the Amazon river

In poor and remote zones of the world, such as the Amazon region, the lack of analytical infrastructures prevents regular quality assessments of water systems. The access to affordable, portable and robust analytical technologies for real-time and on-site water monitoring is, therefore, key to safeguard vulnerable communities and the environment. In this context, we have developed and successfully implemented an electrochemical methodology for the rapid (60 s) and effective simultaneous electrochemical detection of heavy metal ions of concern (Pb2+, Cu2+ and Hg2+) in water, with a single screen-printed electrode probe. In particular, we show a wide quantification range for each pollutant (5−300 μg L−1), and detection limits below the Environmental Protection Agency (EPA) maximum contaminant levels for drinking water: 0.015, 1.3 and 0.002 mg L−1 for Pb2+, Cu2+ and Hg2+, respectively. The electrochemical sensors were tested in high temperature and humidity conditions in remote areas of the Amazon river, highly affected by mining-related heavy metal pollution. The field measurements were validated against standard lab-based analytical methods, showing excellent agreement. Our methodology can lead to an affordable and portable diagnostic tool for rapid and on-site monitoring of heavy metals pollution in remote areas.

A one-pot method for building colloidal nanoparticles into bulk dry powders with nanoscale magnetic, plasmonic and catalytic functionalities

Building easy-to-handle bulk materials with nanoproperties is crucial for many nanotechnology-based real-world applications. Here, we describe a simple one-pot method based on nanoparticle self-assembly of pickering emulsions and in situ polymer deposition for preparing particles consisting of a rigid micro-polymer core covered in exposed surface layers of nanoparticles, which we have named nano-micro-particles (NMPs). Unlike simple colloids, these NMPs can be filtered off from the aqueous suspensions in which they are prepared and dried to form free-flowing powders, which most importantly, retain the properties of the constituent nanoparticles in the surface layer. These NMPs can be stored for extended periods but then used either in the dry state or be re-suspended into liquid media as required. The preparation method is very general and can be readily extended to assemble various types of nanoparticles regardless of their material composition or morphology. In addition, functional components, such as magnetic particles or fluorescent tags, can be encapsulated within the polymer core. This method is a platform technology for building nanoparticles into bulk materials with nano-functionalities tailored toward real-life applications. This is illustrated with examples of the preparation of NMPs suitable for rapid and low-cost on-site water monitoring and remediation.

A fluorimetric nitrite biosensor with polythienothiophene-fullerene thin film detectors for on-site water monitoring.

A novel fluorimetric sensor for highly sensitive nitrite detection on the site is presented in this study. The proposed on-chip approach comprises the use of integrated polymer photodetectors to detect light from fluorescence reactions with a diaminofluorescein probe. The detectors were prepared with a heterostructured nanofilm of polythieno[3,4-b]thiophene/benzodithiophene and (6,6)-phenyl-C71-butyric-acid methyl-ester as a photoactive layer. Prior to fluorimetric detection, the quality of the spin-coated photoactive layer was characterized via nano-morphology and current-density measurements. Nitrite assays were conducted on a poly(methyl methacrylate) microchannel chip, to which polythienothiophene-C71 based detectors were aligned. Results of signal-to-noise ratio determination have indicated a detection limit below 0.55 μM, lower than the 0.1 mg L-1 maximum limit of operation in recirculating aquaculture systems for farming Atlantic salmon Salmo salar. An increase of the nitrite concentration to toxic levels may therefore be possible to detect. The fluorimetric sensor exhibited good linearity over three orders of magnitude and acceptable detection reproducibility, which confirmed its analytical value. Further tests revealed great promise of the integrated biosensor device for detecting nitrite in aquaculture-relevant samples with high precision. The approach reported hereby may provide impetus to in situ analytical tools for monitoring water quality at aquaculture facilities, the food industries or water monitoring stations.

CMAS: fully integrated portable centrifugal microfluidic analysis system for on-site colorimetric analysis

A portable, wireless system capable of in situ reagent-based colorimetric analysis is demonstrated. The system is based on a reconfigurable low cost optical detection method employing a paired emitter detector diode device, which allows a wide range of centrifugal microfluidic layouts to be implemented. Due to the wireless communication, acquisition parameters can be controlled remotely and results can be downloaded in distant locations and displayed in real time. The stand-alone capabilities of the system, combined with the portability and wireless communication, provide the flexibility crucial for on-site water monitoring. The centrifugal microfluidic disc presented here is designed for nitrite detection in water samples, as a proof of principle. A limit of detection of 9.31 ppb, along with similar coefficients of correlation and precision, were obtained from the Centrifugal Microfluidic Analysis System compared with the same parameters measured using a UV-Vis spectrophotometer.