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This paper aims to develop an inexpensive, portable, sensitive and environmentally friendly electrochemical sensor to quantify trace metals.

A sensor was constructed by modifying carbon paste electrode for the determination of lead, cadmium and zinc ions using square wave anodic stripping voltammetry (SWASV). The modified electrode was prepared by inserting homogeneous mixture of 2-hydroxy-acetophenonethiosemicarbazone, graphite powder and mineral oil. Various important parameters controlling the performance of the sensor were investigated and optimized. Electrochemical behavior of modified electrode was characterized by cyclic voltammetry.

Modified carbon pastes electrodes showed three distinct peaks at −0.50, −0.76 and −1.02 V vs silver/silver chloride corresponding to the oxidation of lead, cadmium and zinc ions at the electrode surface, respectively. The highest peak currents for all the metal ions under study were observed in the phosphate buffer solution at pH 1 with a deposition time of 70 s. The sensor exhibited linear behavior in the range of 0.25-12.5 μg mL-1 for lead and cadmium and 0.25-10.0 μg mL⁻¹ for zinc. The limit of detection was calculated as 78.81, 96.17 and 91.88 ng mL⁻¹ for Pb2⁺, Cd2⁺and Zn2⁺, respectively. The modified electrode exhibited good stability and repeatability.

A chemically modified electrode with Schiff base was applied to determine the content of cadmium, lead and zinc ions in aqueous solutions using SWASV.

Advancements in real-time water monitoring technologies permit rapid detection of water quality, and threats from waste loads. Water Framework Directive mandating the establishment of Member States’ water resources monitoring, presence of hazardous contaminants in effluents, and perception of vulnerability of water distribution system to attacks, have spurred technical and economic interests. The paper aims to discuss these issues.

As alternative to traditional analyzers, chemosensors, operate according to physical principles, without sample collection (online), and are capable of supplying parameter values continuously and in real-time. Their low selectivity and stability issues have been overcome by technological developments. This review paper contains a comprehensive survey of existing and expected online monitoring technologies for measurement/detection of pollutants in water.

The state-of-the-art in online water monitoring is presented. Application examples are reported. Monitoring costs will become a lesser part of a water utility budget due to the fact that automation and technological simplification will abate human cost factors, and reduce the complexity of laboratory procedures.

An overview of applicable instrumentation, and forthcoming developments, is given. Technological development in this field is very rapid, and astonishing advances are anticipated in several areas (fingerprinting, optochemical sensors, biosensors, molecular techniques). Online monitoring is becoming an ever-important tool not only for compliance control or plant management purposes, but also as a useful approach to pollution control and reduction, minimizing the environmental impact of discharges.

The purpose of this paper is to review the novel application of surface plasmon resonance (SPR) in sensing heavy metal ions and the development of SPR to become an alternative heavy metal ions sensor.

The possible dangerous toxic effects of heavy metal ions are revealed in the short introduction. The existing conventional methods for sensing heavy metal ions and their drawbacks are also discussed. To overcome these drawbacks, SPR has been investigated from the basic principle to the potential alternative in sensing heavy metal ions.

Application of SPR in sensing heavy metal ions emerged a decade ago. A wide range of active layers or recognition elements (e.g. polymer, protein, nanoparticles) have been developed to combine with SPR. The detection limit, sensitivity and selectivity of SPR sensing in heavy metal ions have been improved from time to time, until the present.

This paper provides up-to-date and systematic information on SPR sensing for heavy metal ions. Different advancements on active layers or recognition molecules have been discussed in detail and arranged in the order of their chronological evolution. The present review may provide researchers with valuable information regarding novel heavy metal ions sensor using SPR and encourage them to take this area for further research and development.

This paper aims to propose a new microfluidic portable experimental platform for quick detection of heavy metal ions (HMIs) in picomolar range. The experimental setup uses a microfabricated piezoresistive sensor (MPS) array of eight cantilevers with ion-selective self-assembled monolayer's (SAM).

Most of the components used in this experimental setup are battery operated and, hence, portable to perform the on-field experiments. HMIs (antigen) and thiol-based SAM (antibody) interaction start bending the microcantilever. This results in a change of resistance, which is directly proportional to the surface stress produced due to the mass of targeted HMIs. The authors have used Cysteamine and 4-Mercaptobenzoic acid as a thiol for creating SAM to test the sensitivity and identify the suitable thiol. Some of the cantilevers are blocked using acetyl chloride to use as a reference for error detection.

The portable experimental platform achieves very small detection time of 10-25 min with a lower limit of detection (LOD) 0.762 ng (6.05 pM) for SAM of Cysteamine and 4-Mercaptobenzoic acid to detect Mn2+ ions. This technique has excellent potential and capability to selectively detect Hg2+ ions as low as 2.43 pM/mL using SAM of Homocysteine (Hcys)-Pyridinedicarboxylic acid (PDCA).

As microcantilever is very thin and fragile, it is challenging to apply a surface coating to have selective detection using Nanadispenser. Some of the cantilevers get broken during this process.

The excessive use and commercialization of NPs are quickly expanding their toxic impact on health and the environment. Also, LOD is limited to nanomolar range. The proposed method used the combination of thin-film, NPs, and MEMS-based technology to overcome the limitation of NPs-based technique and have picomolar range of HMIs detection.

This paper aims to describe the techniques used in industrial optical chemical sensors and to consider future prospects.

This paper discusses the techniques and technologies used in today's optical chemical sensors. It highlights their limitations and considers briefly certain new technological developments.

This paper shows that techniques such as wet reagent‐aided photometry, UV absorption, spectroscopy and UV fluorescence satisfy a range of industrial chemical sensing applications and that optode technology is making limited commercial inroads. It identifies the need for inexpensive, wet reagent‐free chemical sensors and suggests that both solid‐state electrodes and lab‐on‐a‐chip devices may ultimately resolve this issue.

This paper provides a technical insight into the state of optical chemical sensing and illustrates that generic families of inexpensive chemical sensors are yet to be developed.

The Consumer Products Safety Commission in 1976 issued a report [Report PB‐257645 (1976)] with certain recommendations to help prevent lead poisoning in children. They surveyed two hundred studies related to lead poisoning in humans and animals with the objective of establishing a safe level of lead in paint. They concluded that blood lead concentrations of thirty micrograms per decilitre produce the first metabolic effects in children and that absorption of 4.5 milligrams per kilogram per day is associated with blood lead concentrations of 20 micrograms per decilitre. This lead to the conclusion that lead should not be added to paint and that a safe level of lead in paint is considered to be 0.06% by dry weight. The report also discussed the removal of old lead paint and made recommendations as to how this should be done so that both the workmen and the occupants of an area would be safe.

The purpose of this study was to compare the electrodeposition behavior and corrosion resistance of ternary and binary alloys.

Potentiodynamic polarization resistance measurement and anodic linear sweep voltammetry techniques were used for the corrosion study. The surface morphology and chemical composition of the deposits were examined using scanning electron microscopy and atomic absorption spectroscopy, respectively. The phase structure was characterized by X-ray diffraction analysis. Electrodeposition behavior was carried out using cyclic voltammetry and galvanostatic techniques.

It was found that the obtained ternary alloy exhibited better corrosion resistance and a more-preferred surface appearance compared to the binary alloys that were electrodeposited under similar conditions.

The ternary alloy showed better anticorrosion properties compared to binary deposits that were electroplated successfully from the plating baths. The Zn-Co-Fe alloy could be used advantageously in industry because the ternary alloy exhibits the collective properties of the binary alloys in one alloy via the electrodeposition of Zn-Ni-Co alloy.

Increasing the corrosion resistance implies to social economic increases.

To date, the electrodeposition of Zn-Co-Fe alloy was studied in only a small number of articles. It was found that the presence of Co or Fe could provide a useful coating on the steel that would reduce its susceptibility to corrosion attack.

The purpose of this paper is to investigate the corrosion resistance and the electrodeposition behavior of electrodeposited nickel‐cobalt‐iron alloys. Also, to compare the electrodeposition of ternary nickel‐cobalt‐iron alloy from acidic sulfate bath onto a steel substrate with the characteristics of Co‐Fe electrodeposits.

The investigation of electrodeposition was carried out using cyclic voltammetry and galvanostatic techniques, while potentiodynamic polarization resistance and anodic linear sweep voltammetry techniques were used for corrosion study. The phase structure was characterized by means of X‐ray diffraction analysis. The surface morphology and chemical composition of the deposits were examined by using scanning electron microscopy and atomic absorption spectroscopy, respectively.

The obtained results revealed that the Ni‐Co‐Fe alloys consisted of a mixture of iron (Fe10.8Ni) and (FeCo) phases. It was found that the obtained Ni‐Co‐Fe alloy exhibited a more‐preferred surface appearance and better corrosion resistance, compared to the Co‐Fe alloy that was electrodeposited under similar conditions.

Ni‐Co‐Fe alloy was successfully electroplated from a sulfate bath. This alloy showed better anticorrosion properties compared to Co‐Fe deposits. The Ni‐Co‐Fe alloy could be used advantageously in industry, e.g. the automotive industry. The coating also has particular interest due to it is ability to exhibit stable magnetic properties.

The paper evaluates the effect of electrodeposition of the ternary alloy on the corrosion behavior of electroplated steel. To date, there has been little research on this issue. It was found that the presence of Ni could increase the corrosion resistance of steel.