Comparison of CO2 capture by ex-situ accelerated carbonation and in in-situ naturally weathered coal fly ash.

Natural weathering at coal power plants ash dams occurs via processes such as carbonation, dissolution, co-precipitation and fluid transport mechanisms which are responsible for the long-term chemical, physical and geochemical changes in the ash. Very little information is available on the natural carbon capture potential of wet or dry ash dams. This study investigated the extent of carbon capture in a wet-dumped ash dam and the mineralogical changes promoting CO2 capture, comparing this natural phenomenon with accelerated ex-situ mineral carbonation of fresh fly ash (FA). Significant levels of trace elements of Sr, Ba and Zr were present in both fresh and weathered ash. However Nb, Y, Sr, Th and Ba were found to be enriched in weathered ash compared to fresh ash. Mineralogically, fresh ash is made up of quartz, mullite, hematite, magnetite and lime while weathered and carbonated ashes contained additional phases such as calcite and aragonite. Up to 6.5 wt % CO2 was captured by the fresh FA with a 60% conversion of calcium to CaCO3 via accelerated carbonation (carried out at 2 h, 4Mpa, 90 °C, bulk ash and a S/L ratio of 1). On the other hand 6.8 wt % CO2 was found to have been captured by natural carbonation over a period of 20 years of wet disposed ash. Thus natural carbonation in the ash dumps is significant and may be effective in capturing CO2.

A review of mercury pollution in South Africa: current status.

The present paper is a review on the status of mercury (Hg) as a pollutant in South African aquatic ecosystems. Spatial patterns of Hg distribution and bioaccumulation in water resources were investigated by collecting and analyzing multimedia samples for physiochemical and Hg-species determination from 62 sampling sites. The data presented showed a wide range in concentrations, which was expected given the array of environmental parameters, water chemistry and sources of Hg. Generally, higher Hg concentrations were measured in environmental compartments impacted by the major anthropogenic Hg sources which, in South Africa, are largely represented by emissions from coal-fired power stations (i.e. Olifants and Upper Vaal WMAs) and artisanal gold mining (i.e., Inkomati WMA). Ancillary water quality parameters (e.g. pH, temperature, DOC, EC and nutrients) were measured and regressed with the measured Hg concentrations to determine which environmental parameters most influenced regional Hg concentrations. The TotHg (sed) and DOC concentrations were identified as important factors controlling TotHg (aq), while TotHg(sed) were correlated to TotHg (aq). This result is indicative of the combined effects of sediment settling and resuspension in the aquatic environment. In contrast, MeHg (aq) was not correlated to DOC. MeHginvert were correlated to MeHg (sed), while MeHg (fish) were correlated to MeHg (aq) and water quality variables (chlorides--Cl(-) and electrical conductivity--EC). A steady progress has been made in Hg research in South Africa. However, despite the substantial knowledge about Hg toxicity, there are still considerable knowledge gaps on the fate and transport of Hg. Hence, further environmental and human health studies are proposed.

Mercury concentrations at a historically mercury-contaminated site in KwaZulu-Natal (South Africa).

INTRODUCTION: A mercury (Hg) processing plant previously operating in KwaZulu-Natal Province (South Africa) discharged Hg waste into a nearby river system causing widespread contamination since the 1980s. Although the processing plant ceased operation in the 1990s, Hg contamination (due to residual Hg) remains significant. Previous studies in the area since the plant's closure have found elevated Hg concentrations in fish, and that these concentrations were as a direct consequence of widespread contamination of the Hg processing plant operations conducted between the 1980s and 1990s. OBJECTIVES: This study aimed at investigating the impacts of residual Hg almost 20 years after the plant's closure. METHODS: Water, sediment and biota (invertebrates and fish) were collected in water resources in the vicinity of the processing plant to determine the Hg concentrations in these compartments, as a proxy for assessing the extent to which residual Hg that is reintroduced to the water column becomes bioavailable to biota. For water and sediment samples, higher total mercury (TotHg) and methylmercury (MeHg) concentrations were measured at sampling sites immediately downstream of the Hg processing plant when compared to the upstream sites, while concentrations decreased with distance from the plant. Fish MeHg concentrations measured just below the US EPA guideline for Hg in fish muscle tissue. RESULTS: The results show that the historically Hg-contaminated river system is a potential Hg pollution source due to the residual Hg present in sediment. Any dredging of sediment as a form of remediation in the Mngceweni River is not recommended; however, a Hg monitoring programme is recommended for assessing the bioavailability of resuspended Hg from sediment.

Mercury concentrations in water resources potentially impacted by coal-fired power stations and artisanal gold mining in Mpumalanga, South Africa.

Total mercury (TotHg) and methylmercury (MeHg) concentrations were determined in various environmental compartments collected from water resources of three Water Management Areas (WMAs) - viz. Olifants, Upper Vaal and Inkomati WMAs, potentially impacted by major anthropogenic mercury (Hg) sources (i.e coal-fired power stations and artisanal gold mining activities). Aqueous TotHg concentrations were found to be elevated above the global average (5.0 ng/L) in 38% of all aqueous samples, while aqueous MeHg concentrations ranged from below the detection limit (0.02 ng/L) to 2.73 +/- 0.10 ng/L. Total Hg concentrations in surface sediment (0-4 cm) ranged from 0.75 +/- 0.01 to 358.23 +/- 76.83 ng/g wet weight (ww). Methylmercury accounted for, on average, 24% of TotHg concentrations in sediment. Methylmercury concentrations were not correlated with TotHg concentrations or organic content in sediment. The concentration of MeHg in invertebrates and fish were highest in the Inkomati WMA and, furthermore, measured just below the US EPA guideline for MeHg in fish.