Size-classified aerosol-bound heavy metals and their effects on human health risks in industrial and remote areas in Japan.

Airborne aerosols were collected in six size classes (PM<0.1, PM0.1-0.5, PM0.5-1, PM1-2.5, PM2.5-10 and PM>10) to investigate aerosol health risks in remote and industrial areas in Japan. We focused on heavy metals and their water-dispersed fractions. The average concentration of heavy metals was 18 ± 25-86 ± 48 ngm-3 for PM<0.1, 46 ± 19-154 ± 80 for PM0.5-1 ngm-3, 98 ± 49-422 ± 186 ngm-3 for PM1-2.5, 321 ± 305-1288 ± 727 ngm-3 for PM2.5-10 and 65 ± 52-914 ± 339 ngm-3 or PM>10, and these concentrations were higher in industrial areas. Heavy metals emitted from domestic anthropogenic sources were added to the long-range transport component of the aerosols. The water-dispersed fraction of heavy metals contained 3.3-40.1% of the total heavy metals in each size class. The relative contribution of Zn and other species (As, Cd, Cr, Ni, Pb, Mn, V and Cu) increased in the water-dispersed fraction. Smaller particles contained greater proportions of the water-dispersed heavy metal fraction. Carcinogenic risk (CR) and the hazard index (HI) were estimated for each size class. The CR of carcinogens was at acceptable levels (<1 ×10-6) for five particle size fractions. The HI values for carcinogens and noncarcinogens were also below acceptable levels (<1) for the same five size fractions. The estimated CR and HI values were dominated by contributions from the inhalation process.

Reversible adsorption of iridium in lyophilized cells of the unicellular red alga Galdieria sulphuraria.

Iridium (Ir) is one of the rarest elements in the Earth's crust and is valuable in industry due to its high corrosion resistance. In this study, we used lyophilized cells of a unicellular red alga, Galdieria sulphuraria for the selective recovery of small amounts of Ir from hydrochloric acid (HCl) solutions. The Ir recovery efficiency of the lyophilized cells was higher than that of activated carbon and comparable to that of an ion-exchange resin in up to 0.2 M acid. Lyophilized G. sulphuraria cells showed different selectivity from the ion-exchange resin, adsorbing Ir and Fe in 0.2 M HCl solution while the ion-exchange resin adsorbed Ir and Cd. The adsorbed Ir could be eluted with more than 90% efficiency using HCl, ethylenediaminetetraacetic acid, and potassium hydroxide solutions, but could not be eluted using a thiourea-HCl solution. After the elution of Ir with a 6 M HCl solution, lyophilized cells could be reused up to five times for Ir recovery with over 60% efficiency. Scanning electron-assisted dielectric microscopy and scanning electron microscopy revealed that Ir accumulated in the cytosol of the lyophilized cells. X-ray absorption fine structure analysis demonstrated the formation of an outer-sphere complex between Ir and the cellular residues, suggesting the adsorption via ion exchange, and explaining the ability to elute the Ir and reuse the cells. Our results provide a scientific basis for inexpensive and environmentally friendly biosorbents as an alternative to ion-exchange resins for the recovery of Ir.