Objectives. We analyzed differences in pediatric elevated blood lead level incidence before and after Flint, Michigan, introduced a more corrosive water source into an aging water system without adequate corrosion control. Methods. We reviewed blood lead levels for children younger than 5 years before (2013) and after (2015) water source change in Greater Flint, Michigan.We assessed the percentage of elevated blood lead levels in both time periods, and identified geographical locations through spatial analysis. Results. Incidence of elevated blood lead levels increased from 2.4% to 4.9% (P<.05) after water source change, and neighborhoods with the highest water lead levels experienced a 6.6% increase. No significant change was seen outside the city. Geospatial analysis identified disadvantaged neighborhoods as having the greatest elevated blood lead levelincreases andinformed response prioritization during the now-declared public health emergency. Conclusions. The percentage of children with elevated blood lead levels increased after water source change, particularly in socioeconomically disadvantaged neighborhoods. Water is a growing source of childhood lead exposure because of aging infrastructure. (Am J Public Health. 2016;106:283–290. doi:10.2105/AJPH.2015.303003)

https://ajph.aphapublications.org/doi/pdf/10.2105/AJPH.2015.303003

Elevated Blood Lead Levels in Children Associated With the Flint Drinking Water Crisis: A Spatial Analysis of Risk and Public Health Response

A review of the identification and detection of heavy metal ions in the environment by voltammetry.

https://cyberleninka.org/article/n/1509928.pdf

Hybrid carbon based nanomaterials for electrochemical detection of biomolecules

Heavy-metal pollution poses severe threat to ecological systems and presents a great challenge for global sustainability. Portable point-of-care sensing platform for detection/monitoring of heavy-metal pollution in the environment is urgently demanded. Herein, a highly sensitive, robust, and low-cost microfluidic electrochemical carbon-based sensor (μCS) for detection of trace heavy metals is presented. The miniaturized μCS devices are based on a microfluidic paper channel combined with a novel three-dimensional layout with working and counter electrodes facing each other and analyte flowing along the microfluidic channel between these two electrodes. Pristine graphite foil free of any surface modifier is not only used as the electronically conductive pad but also directly employed as the working electrode for fabricating the μCS. The resulting simple and portable device was applied in Cd2+ and Pb2+ detection using square-wave anodic stripping voltammetry. Detection limits down to 1.2 μg/L for Cd2+ and 1....

Modifier-Free Microfluidic Electrochemical Sensor for Heavy-Metal Detection.

The challenge of heavy metal detection for environmental, industrial and medical purposes has led to the development of many analytical techniques. Stripping voltammetry is a very sensitive electrochemical method and has been widely used for heavy metal detection. Carbon nanotubes, a well-studied carbon material with physical and chemical properties suited for electrode material is commonly employed for sensitive and selective metal detection in electrochemistry. This article reviews the recent (2011–2016) applications of carbon nanotubes as an electrode or electrode surface modifier for heavy metals detection with stripping voltammetry.

Carbon nanotubes heavy metal detection with stripping voltammetry: A review paper

Carbon nanofiber electrode array for the detection of lead

To clarify the cis-trans isomerization mechanism of simple alkenes on the triplet excited state surface, the photochemistry of acyclic and cyclic vinyl ketones with a p-methoxyacetophenone moiety as a built-in triplet sensitizer (1 and 2, respectively) was compared. When irradiated, ketone 1 produces its cis-isomer, whereas ketone 2 does not yield any photoproducts. Laser flash photolysis of ketone 1 yields a transient spectrum with λmax ∼ 400 nm (τ ∼ 125 ns). This transient is assigned to the first triplet excited state (T1) of 1, which presumably decays to form a triplet biradical (1BR) that is shorter lived than the triplet ketone. In comparison, laser flash photolysis of 2 reveals two transients (τ ∼ 20 and 440 ns), which are assigned to T1 of 2 and triplet biradical 2BR, respectively. Density functional theory calculations support the characterization of the triplet excited states and the biradical intermediates formed upon irradiation of ketones 1 and 2 and allow a comparison of the physical properties of the biradical intermediates. As the biradical centers in 2BR are stabilized by conjugation, 2BR is more rigid than 1BR. Therefore, the longer lifetime of 2BR can be attributed to less-efficient intersystem crossing to the ground state.

Jendai E. Robinson

Papers

Carbon nanofiber electrode array for the detection of lead

Comparison of the Photochemistry of Acyclic and Cyclic 4-(4-Methoxy-phenyl)-4-oxo-but-2-enoate Ester Derivatives.

Electrochemical Characterization of Vertically Aligned Carbon Nanofiber Arrays Prepared by Hole‐mask Colloidal Lithography