Charting achievements: a two-year retrospective of the society for environmental geochemistry and health (SEGH) and the evolving strategies.

Emerging from the shadow of the COVID-19 pandemic, it is time to ground ourselves and retrospectively assess the recent achievements of SEGH over the past years. This editorial serves as a comprehensive report on the progress made in comparison to the aspirations and goals set by the society's board in 2019 (Watts et al., Environ Geochem Health 42:343-347, 2019) (Fig. 1) and reflects on the state of the SEGH community as it reached its 50th anniversary at the close of 2021 (Watts et al. Environ Geochem Health 45:1165-1171, 2023). The focus lies on how the SEGH community navigated through the extraordinary challenges posed by the COVID-19 pandemic since early 2020, and to what extent the 2023 targets have been met.

Editorial: The society for environmental geochemistry and health (SEGH): 50 years and beyond.

When the SEGH international board released a short editorial paper back in 2019, we described an aim to increase the membership offering, whilst improving the diversity of input regionally, by scientific discipline and to ensure greater and more regular contact across the regions from 2020 onwards. Wider aspirations described in 2019 (Watts et al. 2019) are discussed within this short communication at the end of 2021 to evaluate progress made. In particular, how the SEGH community adapted to the unprecedented circumstances that have challenged each and every one of us throughout the COVID-19 pandemic since early 2020 and are likely to influence our activities for the foreseeable future.

Image-based bidirectional reflectance distribution function measurement.

We present a new image-based process for measuring a surface's bidirectional reflectance rapidly, completely, and accurately. Requiring only two cameras, a light source, and a test sample of known shape, our method generates densely spaced samples covering a large domain of illumination and reflection directions. We verified our measurements both by tests of internal consistency and by comparison against measurements made with a gonioreflectometer. The resulting data show accuracy rivaling that of custom-built dedicated instruments.

Determination of soluble chromium in simulated PWR coolant by differential-pulse adsorptive stripping voltammetry.

An analytical method has been developed for the determination of dissolved chromium at concentrations less than 2 mug/l. in PWR coolant by differential-pulse adsorptive stripping voltammetry at a hanging mercury drop electrode. Concentrations above 2 mug/l. can be determined by appropriate dilution of the sample. The method is based on measurement of the current associated with reduction of a chromium(III)-DTPA (diethylenetriaminepenta-acetic acid) complex adsorbed at the surface of the mercury drop. The effects of boric acid, pH, DTPA concentration, accumulation potential and time were investigated together with the oxidation state of the chromium. No interference was observed from other transition metal ions expected to be present in PWR coolant. No alternative chemical technique of similar sensitivity was available for comparison with the results obtained in solutions containing <1 mug/l. chromium. Recoveries from simulated coolant solutions were greater than 95% and the relative standard deviations for single determinations were in the range 12-25%. The statistical limit of detection at the 95% confidence level was 0.023 mug/l. This method of analysis should prove valuable in corrosion studies and is uniquely capable of following the changes in soluble chromium concentration in PWR coolant that follow operational changes in the reactor.

Differential pulse stripping voltammetry for the determination of nickel and cobalt in simulated PWR coolant.

The determination of ionic nickel and cobalt in simulated PWR coolant at concentrations below 1 microg/l. by differential pulse stripping voltammetry at a hanging mercury-drop electrode has been investigated. The high sensitivity for these ions results from the adsorptive accumulation of their dimethylglyoximate complexes on the mercury drop. Boric acid does not interfere and if the samples are adjusted to pH 9 with an ammonia-ammonium chloride buffer, both nickel and cobalt can be determined in the same run. The relative standard deviations at concentrations below 2 microg/l. are of the order of 5-7% and the limits of detection for nickel and cobalt are about 8 and 2 ng/l. respectively. These performance statistics show that this method is the most sensitive method currently available for determination of soluble nickel and cobalt in PWR coolant and it should prove to be most valuable in any corrosion studies of the materials of construction of the primary circuit of a PWR.