Hydrogen-bond organic-framework-based electrochemical sensor for highly sensitive determination of trace cadmium ions in environmental and e-cigarette samples.

BACKGROUND: The heavy metal ion Cd2+ is acutely toxic, and excessive concentrations can have adverse effects on human production and life, and even lead to significant public health risks and environmental impacts. There are several mature non-electrochemical methods for heavy metal detection, but these methods are characterized by high cost, which makes it difficult to be applied to the field for timely detection. Therefore, it is necessary to prepare a new electrochemical sensor that is environmentally friendly and capable of detecting Cd2+ in the environment quickly, easily and sensitively. RESULTS: In this study, hydrogen-bonded organic frameworks (HOFs) were synthesized by a simple hydrothermal reaction. The prepared materials consisted of only C, N and O and had a thin lamellar structure. The HOFs were integrated into a novel electrochemical sensor to achieve accurate detection of Cd2+ ions in real aqueous environments by square wave anodic dissolution voltammetry. The sensor has a wide linear range and a detection limit as low as 0.13 µg/L. Several real water samples, such as tap water, lake water, and e-cigarette digest, were analyzed to simulate the working environment of the sensor, and the results showed that the recoveries of Cd2+ ranged from 95.75 % to 101.2 %. SIGNIFICANCE: We pioneered the detection of heavy metal ions Cd2+ in e-cigarette digestate samples with the innovative use of HOFs as the sensor material, which demonstrated the potential application in electrochemical sensing with extremely low background current value and high sensitivity, providing new ideas for environmental monitoring and public health control.

Design, modeling and in silico simulation of bacterial biosensors for detecting heavy metals in irrigation water for precision agriculture.

Sensors used in precision agriculture for the detection of heavy metals in irrigation water are generally expensive and sometimes their deployment and maintenance represent a permanent investment to keep them in operation, leaving a lasting polluting footprint in the environment at the end of their lifespan. This represents an area of opportunity to design new biological devices that can replace part, or all of the sensors currently used. In this article, a novel workflow is proposed to fully carry out the complete process of design, modeling, and simulation of reprogrammable microorganisms in silico. As a proof-of-concept, the workflow has been used to design three whole-cell biosensors for the detection of heavy metals in irrigation water, namely arsenic, mercury and lead. These biosensors are in compliance with the concentration limits established by the World Health Organization (WHO). The proposed workflow allows the design of a wide variety of completely in silico biodevices, which aids in solving problems that cannot be easily addressed with classical computing. The workflow is based on two technologies typical of synthetic biology: the design of synthetic genetic circuits, and in silico synthetic engineering, which allows us to address the design of reprogrammable microorganisms using software and hardware to develop theoretical models. These models enable the behavior prediction of complex biological systems. The output of the workflow is then exported in the form of complete genomes in SBOL, GenBank and FASTA formats, enabling their subsequent in vivo implementation in a laboratory. The present proposal enables professionals in the area of computer science to collaborate in biotechnological processes from a theoretical perspective previously or complementary to a design process carried out directly in the laboratory by molecular biologists. Therefore, key results pertaining to this work include the fully in silico workflow that leads to designs that can be tested in the lab in vitro or in vivo, and a proof-of-concept of how the workflow generates synthetic circuits in the form of three whole-cell heavy metal biosensors that were designed, modeled and simulated using the workflow. The simulations carried out show realistic spatial distributions of biosensors reacting to different concentrations (zero, low and threshold level) of heavy metal presence and at different growth phases (stationary and exponential) that are backed up by the whole design and modeling phases of the workflow.

An ultra-efficient pretreatment method adopted LPUV/CoFe2O4/PMS-based photolysis for accurate detection of Cd(II) and Pb(II) in water via SWASV.

Dissolved organic matter (DOM) is a widely occurring substance in rivers that can strongly complex with heavy metal ions (HMIs), severely interfering with the electrochemical signal of anodic stripping voltammetry (ASV) and reducing the detection accuracy of HMIs in water. In this study, we investigated a novel advanced oxidation process (AOP) that involves the activation of peroxymonosulfate (PMS) using low-pressure ultraviolet (LPUV) radiation and CoFe2O4 photocatalysis. This novel AOP was used for the first time as an effective pretreatment method to break or weaken the complexation between HMIs and DOM, thereby restoring the electrochemical signals of HMIs. The key parameters, including the PMS concentration, CoFe2O4 concentration, and photolysis time, were optimized to be 6 mg/L, 12 mg/L, and 30 s for eliminating DOM interference during the electrochemical analysis of HMIs via LPUV/CoFe2O4-based photolysis. Investigations of the microstructure, surface morphology, specific surface area, and pore volume of CoFe2O4 were conducted to reveal the exceptional signal recovery capability of LPUV/CoFe2O4/PMS-based photolysis in mitigating interference from DOM during HMIs analysis. The PMS activation mechanism, which is critical to the signal recovery process, was elucidated by analyzing the reactive oxygen species (ROS) and the surface elemental composition of CoFe2O4. Additionally, the degradation and transformation behavior of humus-HMIs complexes were analyzed to study the mechanism of ASV signal recovery further. Notably, the detection results of HMIs in actual water samples obtained using the proposed pretreatment method were compared with those obtained from ICP-MS, yielding an RMSE less than 0.04 µg/L, which indicated the satisfactory performance of the proposed pretreatment method for the ASV detection of HMIs in complex actual samples.

Photoluminescent Nanocellulosic Film for Selective Hg2+ Ion Detection.

We developed a highly sensitive solid-state sensor for mercury detection by stabilizing red-sub-nanometric fluorescent gold nanoclusters (AuNC, 0.9 ± 0.1 nm diameter) with bovine serum albumin in a matrix composed of cellulose nanofibrils (CNF) (BSA-AuNC/CNF). The main morphological and optical features of the system were investigated via atomic force/transmission electron microscopy and UV-Vis/fluorescence spectroscopy. The hybrid film (off-white and highly transparent) showed strong photoluminescene under UV irradiation. The latter is assigned to the AuNC, which also increase the ductility of the emitting film, which was demonstrated for high sensitivity Hg2+ detection. When used as a sensor system, following AuNC printing on CNF hybrid films, a limit of detection <10 nM was confirmed. What is more, nanocellulose films have a high pore structure and selective separation properties, showcasing a wide range of potential applications in many fields such as water treatment and oil-water separation.

Recent advance of nanomaterials modified electrochemical sensors in the detection of heavy metal ions in food and water.

As one of the main pollutants, heavy metal ions can accumulate in the human body and cause a cascade of damage. Electrochemical sensors provide great prospects for tracing heavy metal ions because of their properties of high sensitivity, low detection limits and fast response. Electrode surface modification materials play a key role in enhancing the performance of electrochemical sensors. Herein, we summarize in detail the recent work on electrochemical sensors modified by carbon nanomaterials (graphene and its derivatives, carbon nanofibers and carbon nanotubes), metal nanomaterials (gold, silver, bismuth and iron), complexes (MOFs, ZIFs and MXenes) and their composites for the detection of heavy metal ions (mainly include Cd(II), Hg(II), Pb(II), As(III), Cu(II) and Zn(II)) in food and water. The synthetic strategies, mechanisms, innovations, advantages, challenges and prospects of various electrode modification nanomaterials for the detection of heavy metal ions in food and water are discussed.

Validation and calibration of a novel GEM biosensor for specific detection of Cd2+, Zn2+, and Pb2.

BACKGROUND: In this study, we designed a novel genetic circuit sensitive to Cd2+, Zn2+ and Pb2+ by mimicking the CadA/CadR operon system mediated heavy metal homeostasis mechanism of Pseudomonas aeruginosa. The regular DNA motifs on natural operon were reconfigured and coupled with the enhanced Green Fluorescent Protein (eGFP) reporter to develop a novel basic NOT type logic gate CadA/CadR-eGFP to respond metal ions mentioned above. A Genetically Engineered Microbial (GEM)-based biosensor (E.coli-BL21:pJET1.2-CadA/CadR-eGFP) was developed by cloning the chemically synthesised CadA/CadR-eGFP gene circuit into pJET1.2-plasmid and transforming into Escherichia coli (E. coli)-BL21 bacterial cells. RESULTS: The GEM-based biosensor cells indicated the reporter gene expression in the presence of Cd2+, Zn2+ and Pb2+ either singly or in combination. Further, the same biosensor cells calibrated for fluorescent intensity against heavy metal concentration generated linear graphs for Cd2+, Zn2+ and Pb2+ with the R2 values of 0.9809, 0.9761 and 0.9758, respectively as compared to non-specific metals, Fe3+ (0.0373), AsO43- (0.3825) and Ni2+ (0.8498) making our biosensor suitable for the detection of low concentration of the former metal ions in the range of 1-6 ppb. Furthermore, the GEM based biosensor cells were growing naturally within the concentration range of heavy metals, at 37 °C and optimum pH = 7.0 in the medium, resembling the characteristics of wildtype E.coli. CONCLUSION: Finally, the novel GEM based biosensor cells developed in this study can be applied for detection of targeted heavy metals in low concentration ranges (1-6 ppb) at normal bacterial physiological conditions.

An efficient pretreatment method based on AgNPs-doped SnO2 photocatalyst for the accurate detection of heavy metals in organic-rich water samples.

Humic acid (HA), the primary composition of natural organic matter (NOM) widely distributed in water and soil, can complex with heavy metal ions (HMIs), i.e., Cd(II) and Pb(II) in this study, which deters the accurate detection of HMIs using square wave anodic stripping voltammetry (SWASV). Hence, in this study, an efficient pretreatment method was proposed to restore the electrochemical signal of Cd(II) and Pb(II) by breaking the complexation based on AgNPs-doped SnO2 photocatalyst combined with LP/UV irradiation. Optimization of the key parameters for electrochemical signal restoration including pH for photolysis, AgNPs doping rate, photocatalyst dosage and photolysis time were performed to further elevating the accuracy in the proposed pretreatment method over 96.9% for Cd(II) and Pb(II) in 15 min. The effect of different HA concentrations on SWASV signal of Cd(II) and Pb(II) was also investigated adopting the optimal parameters. Then, the UV-vis absorption spectra, crystal structure, and the morphology of AgNPs-doped SnO2 photocatalyst were investigated to excavate the reasons behind the most excellent AgNPs doping rate to SnO2 in signal restoration. Moreover, the behavior of HA degradation and transformation under LP/UV irradiation was studied to investigate the mechanism of electrochemical signal restoration. Finally, the feasibility of the proposed method was testified by comparing detection results with ICP-MS results using real water samples extracted from aquaculture water.

Recent Progress on Fluorescent Probes in Heavy Metal Determinations for Food Safety: A Review.

One of the main challenges faced in food safety is the accumulation of toxic heavy metals from environmental sources, which can sequentially endanger human health when they are consumed. It is invaluable to establish a practical assay for the determination of heavy metals for food safety. Among the current detection methods, technology based on fluorescent probes, with the advantages of sensitivity, convenience, accuracy, cost, and reliability, has recently shown pluralistic applications in the food industry, which is significant to ensure food safety. Hence, this review systematically presents the recent progress on novel fluorescent probes in determining heavy metals for food safety over the past five years, according to fluorophores and newly emerging sensing cores, which could contribute to broadening the prospects of fluorescent materials and establishing more practical assays for heavy metal determinations.

Valorised polypropylene waste based reversible sensor for copper ion detection in blood and water.

Heavy metals and plastic pollutants are the two most disastrous challenges to the environment requiring immediate actions. In this work, a techno-commercially feasible approach to address both challenges is presented, where a waste polypropylene (PP) based reversible sensor is produced to selectively detect copper ions (Cu2+) in blood and water from different sources. The waste PP-based sensor was fabricated in the form of an emulsion-templated porous scaffold decorated with benzothiazolinium spiropyran (BTS), which produced a reddish colour upon exposure to Cu2+. The presence of Cu2+ was checked by naked eye, UV-Vis spectroscopy, and DC (Direct Current) probe station by measuring the current where the sensor's performance remained unaffected while analysing blood, water from different sources, and acidic or basic environment. The sensor exhibited 1.3 ppm as the limit of detection value in agreement with the WHO recommendations. The reversible nature of the sensor was determined by cyclic exposure of the sensor towards visible light turning it from coloured to colourless within 5 min and regenerated the sensor for the subsequent analysis. The reversibility of the sensor through exchange between Cu2+- Cu+ was confirmed by XPS analysis. A resettable and multi-readout INHIBIT logic gate was proposed for the sensor using Cu2+ and visible light as the inputs and colour change, reflectance band and current as the output. The cost-effective sensor enabled rapid detection of the presence of Cu2+ in both water and complex biological samples such as blood. While the approach developed in this study provides a unique opportunity to address the environmental burden of plastic waste management, it also allows for the possible valorization of plastics for use in enormous value-added applications.

Activated carbon based paste electrodes for the simultaneous and effective detection of divalent cadmium and lead ions in wastewater.

Heavy metals (HM) have gained significant attention in terms of regular monitoring and detection owing to their toxicity, non-biodegradability, and persistence. Current techniques for detecting HM are expensive, cumbersome, and require sophisticated instruments and skilled labour. Hence, developing cheap, rapid, energy-efficient, and accurate sensors is imperative and electrochemical techniques have emerged as promising tools. The current study involves the fabrication of an electrochemical sensor for the concurrent detection of lead (Pb2+) and cadmium (Cd2+) ions using modified carbon paste electrodes (mCPE). Activated carbon (AC) with a BET surface area of 1118 m2 g-1 was obtained by chemical activation and thermal treatment of the waste rubberwood sawdust. AC-Graphite, AC-Reduced Graphene Oxide (RGO), and AC-RGO-Chitosan were the types of mCPEs that were utilised. The electrochemical behaviours and effects of pH, concentration, and scan rate were studied using Cyclic voltammetry (CV). Studies on detection were conducted using CV and linear sweep voltammetry. Although all the 3 mCPEs detected Cd2+ and Pb2+ in the simulated wastewater, the CPE with RGO and AC could detect Cd2+ as low as 10.91 µg L-1 and Pb2+ as low as 14.01 µg L-1. The work explored the possibility of using AC as a potential sustainable substitute for graphite in CPE.

Agarose Film-Based Liquid-Solid Conversion for Heavy Metal Detection of Water Samples by Laser-Induced Breakdown Spectroscopy.

Laser-induced breakdown spectroscopy (LIBS) shows promising applications in the analysis of environmental heavy metals. However, direct analysis in water by LIBS faces the problems of droplet splashing and laser energy decay. In this study, a novel liquid-solid conversion method based on agarose films is proposed to provide an easy-to-operate and sensitive detection of heavy metals. First, the water samples were converted into semi-solid hydrogels with the aid of agarose and then dried into agarose films to make the signal intensities stronger. The calibration curves of Cd, Pb and Cr were constructed. The proposed method was validated by standard heavy metal solutions and real water samples. The results showed that the values of R2 were 0.990, 0.989 and 0.975, and the values of the LOD were 0.011, 0.122 and 0.118 mg L-1 for Cd (I) 228.80, Pb (I) 405.78 and Cr (I) 427.48 nm, respectively. The RMSEs of validation were 0.068 (Cd), 0.107 (Pb) and 0.112 mg·L-1 (Cr), and the recovery values were in the range of 91.2-107.9%. The agarose film-based liquid-solid conversion method achieved the desired ease of operation and sensitivity of LIBS in heavy-metal detection, thereby, showing good application prospects in heavy metal monitoring of water.

Dual Emission Carbon Dots for Simultaneous Detections of Pb2+ and Fe3+ Ions in Water Via Distinct Sensing Mechanisms.

Herein, dual-emission carbon dots (DE-CDs) were synthesized using a one-pot hydrothermal method. DE-CDs exhibited two well-separated peaks at 433 and 513 nm under ultraviolet excitation. The prepared DE-CDs offer selective detection of Fe3+ ions via inner filter effect (IFE) and Pb2+ ions via aggregation-induced enhancement (AIE). The obtained DE-CDs showed a good affinity for both Fe3+ and Pb2+ ions in the presence of various interfering ions. The limits of detection were 0.797 ppm and 4.739 ppm for Pb2+ and Fe3+, respectively. The finding reveals the huge potential of DE-CDs for the selective detection of multiple targets in one solution.

Low-pressure ultraviolet-H2O2 photolysis for restoring the anodic stripping voltammetry signal: a new strategy for the detection of heavy metal ions in complex organic matter.

A new strategy based on low-pressure ultraviolet (LPUV)-H2O2 advanced oxidation photolysis for the quantitative determination of organic heavy metal ions (HMIs) in soil was proposed for the efficient, low-cost, accurate, and green detection of Pb(II) and Cd(II) in soil extracts by breaking the complexation of HMIs and organic matters, consequently restoring the ASV signals of target HMIs. The key parameters of the proposed LPUV-H2O2 photolysis system for the restoration of stripping responses were optimized; the conversion of organic matter to inorganic matter during the photolysis was investigated by total organic carbon (TOC); the degradation kinetics of humic acid sodium (HAS) was measured by UV-vis spectroscopy (UV); the pathway of HAS converted to small molecule organics during degradation was observed by fluorescence spectroscopy (FS); additionally, Fourier transform infrared spectroscopy (FTIR) was used to study the complexation between HAS and HMIs. The results showed that the stripping signals of target HMIs in the simulated soil samples can be restored to nearly 100% with a good repeatability, and the restoration ratio of the stripping signal fluctuated within 10%. And the feasibility of the proposed method for the accurate detection of HMIs in the real soil samples was verified; the results showed that 93.7% of Cd(II) and 92.5% of Pb(II) in real soil extracts were detectable.

Recent Advancement in Disposable Electrode Modified with Nanomaterials for Electrochemical Heavy Metal Sensors.

Heavy metal pollution has gained global attention due to its high toxicity and non-biodegradability, even at a low level of exposure. Therefore, the development of a disposable electrode that is sensitive, simple, portable, rapid, and cost-effective as the sensor platform in electrochemical heavy metal detection is vital. Disposable electrodes have been modified with nanomaterials so that excellent electrochemical properties can be obtained. This review highlights the recent progress in the development of numerous types of disposable electrodes modified with nanomaterials for electrochemical heavy metal detection. The disposable electrodes made from carbon-based, glass-based, and paper-based electrodes are reviewed. In particular, the analytical performance, fabrication technique, and integration design of disposable electrodes modified with metal (such as gold, tin and bismuth), carbon (such as carbon nanotube and graphene), and metal oxide (such as iron oxide and zinc oxide) nanomaterials are summarized. In addition, the role of the nanomaterials in improving the electrochemical performance of the modified disposable electrodes is discussed. Finally, the current challenges and future prospect of the disposable electrode modified with nanomaterials are summarized.

Release of free-state ions from fulvic acid-heavy metal complexes via VUV/H2O2 photolysis: Photodegradation of fulvic acids and recovery of Cd2+ and Pb2+ stripping voltammetry currents.

Fulvic acid (FA), a ubiquitous organic matter in the environment, can enhance the mobility and bioavailability of Cd2+ and Pb2+ through competitive complexation to form FA-heavy metal ions (FA-HMIs) complexes with excellent solubility. Because FA-HMIs are electrochemically inactive, square wave anodic stripping voltammetry (SWASV) cannot accurately detect the content of bioavailable Cd2+ and Pb2+ in soils and sediments. This study ostensibly aimed to efficiently recover SWASV signals of Cd2+ and Pb2+ in FA-HMIs by disrupting FA-HMIs complexes using the combined vacuum ultraviolet and H2O2 (VUV/H2O2) process. Essentially, this study explored the photodegradation behavior and photolysis by-products of FA and their effects on the conversion of FA-HMIs complexes to free-state Cd2+ and Pb2+ using multiple characterization techniques, as well as revealed the complexation mechanism of FA with Cd2+ and Pb2+. Results showed that reactive groups such as carboxyl and hydroxyl endowed FA with the ability to complex Cd2+ and Pb2+. After FA-HMIs underwent VUV/H2O2 photolysis for 9 min at 125 mg/L of H2O2, FA was decomposed into small molecular organics while removing its functional groups, which released the free-state Cd2+ and Pb2+ and recovered their SWSAV signals. However, prolonged photolytic mineralization of FA to inorganic anions formed precipitates with Cd2+ and Pb2+, thereby decreasing their SWSAV signals. Moreover, the VUV/H2O2 photolysis significantly improved the SWASV detection accuracy toward the Cd2+ and Pb2+ in real soil and sediment samples, verifying its practicality.

Magnetic Nanoparticles as Effective Heavy Ion Adsorbers in Natural Samples.

This paper refers to research based on tests completed on the adsorption of heavy metal ions (Pb2+, Cu2+, Cd2+) from selected natural liquid samples such as apple, tomato, and potato juices using surface-functionalized Mn ferrite nanoparticles (Mn0.2Fe2.8O4). To determine the most efficient adsorption conditions of these heavy metals, the nanoparticles' surfaces were modified with five different ligands (phthalic anhydride, succinic anhydride, acetic anhydride, 3-phosphonopropionic acid, and 16-phosphonohexadecanoic acid). To evaluate the success of the adsorption process, the resultant liquid samples were examined for the amount of residuals using the flame atomic absorption spectroscopy method. The Mn ferrite particles selected for these tests were first characterized physicochemically by the following methods: transmission electron microscopy, scanning electron microscopy, X-ray diffraction, IR spectroscopy, Mössbauer spectroscopy.

Adsorptive preconcentration integrated with colorimetry for ultra-sensitive detection of lead and copper.

This work proposes a novel detection method for the ultra-sensitive colorimetric determination of lead and copper in complex water matrix. The method integrates signal amplification with analytical sensing, achieved by adsorptive preconcentration and a colorimetric assay. We report for the first time a strategic application of batch adsorption as a preconcentration method and colorimetry performed directly on the adsorbent surface enriched with metal. Commercially available kaolin was used as the adsorbent to preconcentrate the metals. The colorimetric detection of Pb and Cu was achieved using sodium rhodizonate and bathocuproine salt as chromogenic indicators, respectively. This method eliminates the involvement of complex instrumentation and the need for new sensing material preparation. The proposed method possesses high sensitivity for both Pb and Cu under optimized conditions. A linear calibration curve is obtained in two concentration ranges, spanning 1 to 100 µg L-1 with a low detection limit of 0.6 and 1.2 µg L-1 for Pb and Cu, respectively. Further, the method enables visual detection of Pb at concentrations as low as 2.5 µg L-1 by the naked eye. We demonstrate the practical applicability of the method by simultaneous detection of Pb and Cu in six different real-water samples with good apparent recovery % [90-120%]. Detection using hand-held devices indicates the feasibility for on-site analysis. Overall, this platform method offers a high scope for de-centralized monitoring of pollutants at concentrations which are prevailing in the environment. Integrating adsorptive preconcentration with colorimetric assay enables quantitative metal detection in environmental water sample matrix.

A Recombinase-Based Genetic Circuit for Heavy Metal Monitoring.

Rapid progress in the genetic circuit design enabled whole-cell biosensors (WCBs) to become prominent in detecting an extensive range of analytes with promise in many fields, from medical diagnostics to environmental toxicity assessment. However, several drawbacks, such as high background signal or low precision, limit WCBs to transfer from proof-of-concept studies to real-world applications, particularly for heavy metal toxicity monitoring. For an alternative WCB module design, we utilized Bxb1 recombinase that provides tight control as a switch to increase dose-response behavior concerning leakiness. The modularity of Bxb1 recombinase recognition elements allowed us to combine an engineered semi-specific heat shock response (HSR) promoter, sensitive to stress conditions including toxic ions such as cadmium, with cadmium resistance regulatory elements; a cadmium-responsive transcription factor and its cognitive promoter. We optimized the conditions for the recombinase-based cadmium biosensor to obtain increased fold change and shorter response time. This system can be expanded for various heavy metals to make an all-in-one type of WCB, even using semi-specific parts of a sensing system.

Fluorescent and colorimetric assay for determination of Cu(II) and Hg(II) using AuNPs reduced and wrapped by carbon dots.

To improve the accuracy and specificity of visual sensors for detecting Cu(II) and Hg(II), a fluorescent and colorimetric dual-modal sensor based on Au nanoparticles (AuNPs) prepared by using carbon dots (CDs) was designed. If a sensor is to be applied for the detection of targets in different environmental backgrounds, it needs to have high stability against heat, pH, and salt. To this end, CD-wrapped AuNP probes were fabricated by the in situ reaction of chloroauric acid and reductive CDs. The reductive CDs were prepared with hyperbranched polyethyleneimine (HPEI) as a carbon source. HPEI-CDs not only acted as a reducing agent but also as an excellent stabilizer in the preparation and detection application of the AuNPs. Based on multiple signal responses, including color, UV-Vis absorption, and fluorescence intensity, the HPEI-CD/AuNP nanosensor was used to realize the detection of Cu2+ and Hg2+ in the linear range 9.0×10-10-9.0×10-4 M and 9.0×10-7-9.0×10-5 M with low detection limits of 75.6 nM and 281 nM, respectively. In tap water analysis, the recovery of Cu2+ and Hg2+ by fluorescent range from 109.98-113.31% and 100.65-100.81%, and the RSD values were 0.1159-1.6317% and 3.2-5.4%, respectively. The recovery of Cu2+ and Hg2+ by colorimetric detection were 99.72-100.14% and 99.88-100.12%, and RSD values were 0.6527-0.6842% and 0.4400-0.8386%, respectively. Importantly, this sensor was applied to the accurate and sensitive detection of Cu2+ and Hg2+ in tap water and sea water. The multimode readout nanosensor exhibited strong potential for achieving simultaneous detection of two different heavy metal ions in practical applications. The novel multi-mode readout carbon dots/AuNPs sensor for Cu2+ and Hg2+ detectionshowed high sensitivity and selectivity.

Development of Cd (II) Ion Probe Based on Novel Polyaniline-Multiwalled Carbon Nanotube-3-aminopropyltriethoxylsilane Composite.

Cadmium belongs to the group of potentially toxic metals that have high health and environmental significance. Due to its adverse effects on the environment, this study develops an effective electrochemical sensor for detecting a polyaniline-multiwalled carbon nanotube-3-aminopropyltriethoxysilane (PANI-MWCNT-APTES) substrate cast on the GCE. The as-prepared PANI-MWCNT-APTES was prepared by a wet chemical method, and its formation was investigated using several techniques. As a result, the prepared material exhibited a limit of detection of 0.015 µM for cadmium ions (Cd2+) in the linear dynamic range of 0.05 µM to 50 µM. Furthermore, the PANI-MWCNT-APTES-modified GCE current response was stable, repeatable, reproducible, and short. In addition, PANI-MWCNT-APTES/GCE was harnessed for the first time for cadmium detection in real water samples, and the result was satisfactory. Therefore, the recorded results suggest that the newly designed PANI-MWCNT-APTES is a promising material for detecting Cd in the near future for human health and environmental protection.