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1.
Environ Sci Technol ; 56(19): 13546-13564, 2022 10 04.
Article in English | MEDLINE | ID: mdl-36121207

ABSTRACT

Most soil quality measurements have been limited to laboratory-based methods that suffer from time delay, high cost, intensive labor requirement, discrete data collection, and tedious sample pretreatment. Real-time continuous soil monitoring (RTCSM) possesses a great potential to revolutionize field measurements by providing first-hand information for continuously tracking variations of heterogeneous soil parameters and diverse pollutants in a timely manner and thus enable constant updates essential for system control and decision-making. Through a systematic literature search and comprehensive analysis of state-of-the-art RTCSM technologies, extensive discussion of their vital hurdles, and sharing of our future perspectives, this critical review bridges the knowledge gap of spatiotemporal uninterrupted soil monitoring and soil management execution. First, the barriers for reliable RTCSM data acquisition are elucidated by examining typical soil monitoring techniques (e.g., electrochemical and spectroscopic sensors). Next, the prevailing challenges of the RTCSM sensor network, data transmission, data processing, and personalized data management are comprehensively discussed. Furthermore, this review explores RTCSM data application for updating diverse strategies including high-fidelity soil process models, control methodologies, digital soil mapping, soil degradation, food security, and climate change mitigation. Finally, the significance of RTCSM implementation in agricultural and environmental fields is underscored through illuminating future directions and perspectives in this systematic review.


Subject(s)
Environmental Pollutants , Soil , Agriculture
2.
Environ Sci Technol ; 56(8): 4905-4914, 2022 04 19.
Article in English | MEDLINE | ID: mdl-35274533

ABSTRACT

Accurate and continuous monitoring of soil nitrogen is critical for determining its fate and providing early warning for swift soil nutrient management. However, the accuracy of existing electrochemical sensors is hurdled by the immobility of targeted ions, ion adsorption to soil particles, and sensor reading noise and drifting over time. In this study, polyacrylamide hydrogel with a thickness of 0.45 µm was coated on the surface of solid-state ion-selective membrane (S-ISM) sensors to absorb water contained in soil and, consequently, enhance the accuracy (R2 > 0.98) and stability (drifting < 0.3 mV/h) of these sensors monitoring ammonium (NH4+) and nitrate (NO3-) ions in soil. An ion transport model was built to simulate the long-term NH4+ dynamic process (R2 > 0.7) by considering the soil adsorption process and soil complexity. Furthermore, a soil-based denoising data processing algorithm (S-DDPA) was developed based on the unique features of soil sensors including the nonlinear mass transfer and ion diffusion on the heterogeneous sensor-hydrogel-soil interface. The 14 day tests using real-world soil demonstrated the effectiveness of S-DDPA to eliminate false signals and retrieve the actual soil nitrogen information for accurate (error: <2 mg/L) and continuous monitoring.


Subject(s)
Ammonium Compounds , Nitrogen , Hydrogels , Nitrates/analysis , Nitrogen/analysis , Soil
3.
J Hazard Mater ; 400: 123299, 2020 12 05.
Article in English | MEDLINE | ID: mdl-32947704

ABSTRACT

Lead (Pb) contaminants in wastewater have inhibited microbial activities and thus exerted high energy consumption in wastewater treatment plants (WWTPs). Current Pb monitoring has been conducted ex situ and off line, unable to affect real-time proactive control and operation. This study targets the crucial challenge of better and faster Pb monitoring by developing novel mm-sized screen-printed solid-state ion-selective membrane (S-ISM) Pb sensors with low-cost, high accuracy and long-term durability and that enable real-time in situ monitoring of Pb(II) ion contamination down to low concentrations (15 ppb-960 ppb) in wastewater. An innovative pH auto-correction data-driven model was built to overcome the inextricable pH inferences on Pb(II) ISM sensors in wastewater. Electrochemical impedance spectroscopy (EIS) and cyclic voltammograms (CV) analysis showed (3,4-ethylenedioxythiophene, EDOT) deposited onto the mm-sized screen-printed carbon electrodes using electropolymerization effectively alleviated the interferences from dissolved oxygen and improved long-term stability in wastewater. Monte Carlo simulation of the nitrification process predicted that real-time, and high accurate in situ monitoring of Pb(II) in wastewater and swift feedback control could save ∼53 % of energy consumption by alleviating the errors from pH and DO impacts in WWTPs.

4.
ACS Sens ; 5(10): 3182-3193, 2020 10 23.
Article in English | MEDLINE | ID: mdl-32933249

ABSTRACT

Long-term accurate and continuous monitoring of nitrate (NO3-) concentration in wastewater and groundwater is critical for determining treatment efficiency and tracking contaminant transport. Current nitrate monitoring technologies, including colorimetric, chromatographic, biometric, and electrochemical sensors, are not feasible for continuous monitoring. This study addressed this challenge by modifying NO3- solid-state ion-selective electrodes (S-ISEs) with poly(tetrafluoroethylene) (PTFE, (C2F4)n). The PTFE-loaded S-ISE membrane polymer matrix reduces water layer formation between the membrane and electrode/solid contact, while paradoxically, the even more hydrophobic PTFE-loaded S-ISE membrane prevents bacterial attachment despite the opposite approach of hydrophilic modifications in other antifouling sensor designs. Specifically, an optimal ratio of 5% PTFE in the S-ISE polymer matrix was determined by a series of characterization tests in real wastewater. Five percent of PTFE alleviated biofouling to the sensor surface by enhancing the negative charge (-4.5 to -45.8 mV) and lowering surface roughness (Ra: 0.56 ± 0.02 nm). It simultaneously mitigated water layer formation between the membrane and electrode by increasing hydrophobicity (contact angle: 104°) and membrane adhesion and thus minimized the reading (mV) drift in the baseline sensitivity ("data drifting"). Long-term accuracy and durability of 5% PTFE-loaded NO3- S-ISEs were well demonstrated in real wastewater over 20 days, an improvement over commercial sensor longevity.


Subject(s)
Ion-Selective Electrodes , Wastewater , Fluorocarbons , Nitrates/analysis , Polytetrafluoroethylene
5.
Water Res ; 165: 114971, 2019 Nov 15.
Article in English | MEDLINE | ID: mdl-31442758

ABSTRACT

High energy consumption is a critical problem for wastewater treatment systems currently monitored using conventional "single point" probes and operated with manual or automatic open-loop control strategies, exhibiting significant time lag. This challenge is addressed in this study by profiling the variation of three critical water quality parameters (conductivity, temperature and pH) along the depth of a reactor at high spatiotemporal resolution in a real-time mode using flat thin milli-electrode array (MEA) sensors. The profiling accurately captured the heterogeneous status of the reactor under transient shocks (conductivity and pH) and slow lingering shock (temperature), providing an effective dataset to optimize the chemical dosage and energy requirement of wastewater treatment systems. Transient shock models were developed to validate the MEA profiles and calculate mass transfer coefficients. Monte Carlo simulation revealed high-resolution MEA profiling combined with fast closed-loop control strategies can save 59.50% of energy consumption (Temperature and oxygen consumption controls) and 45.29% of chemical dosage, and reach 16.28% performance improvement over the benchmark (defined with ideal conditions), compared with traditional "single-point" sensors that could only monitor the entire system through a single process state. This study demonstrated the capability of MEA sensors to profile reactor heterogeneity, visualize the variation of water quality at high resolution, provide complete datasets for accurate control, and ultimately lead to energy-saving operation with high resilience.


Subject(s)
Waste Disposal, Fluid , Wastewater , Electrodes
6.
Water Res X ; 4: 100028, 2019 Aug 01.
Article in English | MEDLINE | ID: mdl-31334492

ABSTRACT

Novel flexible thin mm-sized resistance-typed sensor film (MRSF) fabricated using ink-jet printing technology (IPT) was developed in this study to monitor water flow rate in pipelines in real time in situ mode. The mechanism of MRSF is that the mm-sized interdigitated electrodes made by printing silver nanoparticles on an elastic polyimide film bend under different flow rates, leading to variation of the resistance of the sensor at different degrees of curvature. Continuous flow tests showed that MRSF possessed a high accuracy (0.2 m/s) and excellent sensitivity (0.1447/ms-1). A model of sensor resistance and flow velocity was established to unfold the correlation between the fundamentals of fluid mechanics and the mechanic flexibility of sensor materials. An analytical model yielded a high coefficient of determination (R2 > 0.93) for the relationship between the resistance increment of the MRSF and the square of the flow velocity at the velocity range of 0.25-2 m/s. Furthermore, a temperature-correction model was developed to quantify the effect of water temperature on the sensor resistance readings. MRSF exhibited a low temperature coefficient of resistance (TCR, 0.001) at the water temperature range of 20-60 °C. Computational fluid dynamics (CFD) simulations using the finite element method were conducted and confirmed both the underlying load assumptions and the deformation characteristics of the sensor film under various flow and material conditions. High-resolution monitoring of water flow rate using MRSF technology was expected to save at least 50% energy consumption for a given unit, especially under flow fluctuation. MRSF possesses a great potential to perform real-time in situ monitoring at high accuracy with ultralow cost, thus enabling the feedback control at high spatiotemporal resolution to reduce the overall energy consumption in water and wastewater systems.

7.
Environ Sci Technol ; 53(6): 3140-3148, 2019 03 19.
Article in English | MEDLINE | ID: mdl-30807116

ABSTRACT

Real-time, in situ accurate monitoring of nitrogen contaminants in wastewater over a long-term period is critical for swift feedback control, enhanced nitrogen removal efficiency, and reduced energy consumption of wastewater treatment processes. Existing nitrogen sensors suffer from high cost, low stability, and short life times, posing hurdles for their mass deployment to capture a complete picture within heterogeneous systems. Tackling this challenge, this study presents solid-state ion-selective membrane (S-ISM) nitrogen sensors for ammonium (NH4+) and nitrate (NO3-) in wastewater that were coupled to a wireless data transmission gateway for real-time remote data access. Lab-scale test and continuous-flow field tests using real municipal wastewater indicated that the S-ISM nitrogen sensors possessed excellent accuracy and precision, high selectivity, and multiday stability. Importantly, autocorrections of the sensor readings on the cloud minimized temperature influences and assured accurate nitrogen concentration readings in remote-sensing applications. It was estimated that real-time, in situ monitoring using wireless S-ISM nitrogen sensors could save 25% of electric energy under normal operational conditions and reduce 22% of nitrogen discharge under shock conditions.


Subject(s)
Ammonium Compounds , Wastewater , Nitrates , Nitrogen , Waste Disposal, Fluid
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