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This paper reports the distribution of Polycyclic Aromatic Hydrocarbons (PAHs) in wash-off in urban stormwater in Gold Coast, Australia. Runoff samples collected from residential, industrial and commercial sites were separated into a dissolved fraction (<0.45 microm), and three particulate fractions (0.45-75 microm, 75-150 microm and >150 microm). Patterns in the distribution of PAHs in the fractions were investigated using Principal Component Analysis. Regardless of the land use and particle size fraction characteristics, the presence of organic carbon plays a dominant role in the distribution of PAHs. The PAHs concentrations were also found to decrease with rainfall duration. Generally, the 1- and 2-year average recurrence interval rainfall events were associated with the majority of the PAHs and the wash-off was a source limiting process. In the context of stormwater quality mitigation, targeting the initial part of the rainfall event is the most effective treatment strategy. The implications of the study results for urban stormwater quality management are also discussed.

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Phosphate is a minor but important constituent of iron ores and is especially undesirable in the production of steel where it is considered a penalty element and is therefore tightly controlled. Iron ore quality must be determined at source, which means that deleterious elements must be accurately determined as an ongoing process. This demands fast, reliable analytical methods for the determination of, amongst others, phosphorus. However, such analysis is severely hampered by the following factors: the standard analytical method employed is X-ray fluorescence (XRF), but the measurements for phosphorus are seriously affected by matrix and inter-element interferences. An alternative technique is inductively coupled plasma with optical emission spectroscopy (ICP-OES), but there are also complications in using ICP-OES. The abundance of phosphorus in rocks is very low, generally under 0.5% wt. ICP-OES is also very insensitive to phosphorus and therefore must use the most sensitive spectral lines for quantification, and, there are serious spectral interferences on these lines by Fe and Cu. This study examines several analytical approaches for the determination of phosphate, using preparation by fusion and analysis by ICP-OES, demonstrating that suitable mathematical procedures and software applications can produce good results for phosphates, comparable to inter-laboratory tests or XRF.

Tungsten is a critical element used in the industry with increasing global demand. There are millions of tons of current and legacy mineral processing tungsten tailings worldwide that can potentially contaminate the environment and pose human health risks. These tailings could also potentially turn into valuable resources if we thoroughly characterise their geochemical composition. In this study, an innovative method was developed to achieve the complete digestion of tungsten tailings. We tested three different digestion methods (hotplate digestion, bomb digestion, and ColdBlockTM digestion) and compared the results. Additionally, an alkali fusion for major element analysis was also applied and tested. The results showed that alkali fusion is the best method for major elements analysis, while bomb digestion is the best method for tungsten and trace element analysis, but volatile chlorite loss was also observed. The hot plate digestion method for tungsten mine tailings was not recommended, because of poor recoveries of trace elements compared to the bomb digestion method. The quick and safer ColdBlockTM digestion method could be used for Bismuth (Bi), Molybdenum (Mo), and several rare earth element analyses indicated by their recoveries being close to the bomb digestion method.