Long-term leaching of As, Cd, Mo, Pb, and Zn from coal fly ash in column test.

Globally, millions of tons of coal fly ash (CFA) are generated per year, and the majority of this material is usually stored in stock piles or landfills, and in a long-term, it can be an environmental hazard if rainwater infiltrates the ashes. Long-term leaching studies of Brazilian ashes are scarce. The purpose of this study was to evaluate arsenic, cadmium, molybdenum, lead, and zinc leaching behavior from a Brazilian CFA by a column experiment designed to simulate field conditions: slightly acid rain considering seasonality of precipitation and temperature for a long-term leaching period (336 days). All elements were leached from CFA, except lead. Elements leaching behavior was influenced by leaching time, leaching volume, and temperature. Higher leachability of As and Cd from CFA during warm and wet season was observed. Results indicate a potential risk to soil and groundwater, since ashes are usually stored in uncovered fields on power plants vicinity.

Abrasiveness evaluation of silica and calcium carbonate used in the production of dentifrices.

Our purpose was to apply a radiometric method to an abrasiveness evaluation in samples of silica and calcium carbonate used as an abrasive in a dentifrice, to help in a prudent selection of materials by dentifrice producers. The results of RDA (radioactive dentin abrasion) abrasiveness indices obtained for these compounds varied from 136 to 19. The relative standard deviations of these RDA results varied from 5.9% to 11.8%, showing a good precision in the method. Also, the results obtained indicated that the abrasiveness indices increase with the particle size of the material. A comparison between different abrasives with similar particle sizes showed that silica presents higher RDA values than calcium carbonate.

Single-step purification of recombinant human growth hormone (hGH) directly from bacterial osmotic shock fluids, for the purpose of (125)I-hGH preparation.

A good quality tracer, to be used in the radioimmunoassay of human growth hormone, was prepared by applying the chloramine-T iodination technique to the recombinant product obtained after a single-step high-performance size-exclusion chromatography purification of a bacterial osmotic shock fluid. The labeling reaction presented a yield of about 65% and the purified tracer exhibited an antibody binding of approximately 50% (NIDDK reference antiserum diluted 1:600,000). These values are very similar to those obtained by radioiodinating highly purified clinical-grade recombinant human growth hormone obtained from the same periplasmic extract after the regular six-step purification process. Both tracers provided the same accuracy, when evaluated with the use of commercial-quality control samples in a classical radioimmunoassay methodology, their stability being practically identical: about 18% decrease in antibody binding after 2 months of storage at -20 degrees C. The novel approach permits the utilization of transformed Escherichia coli strains as a source of freshly prepared, radioiodination-grade recombinant proteins, capable of providing better reproducibility and reagent continuity.

High-yield purification of biosynthetic human growth hormone secreted in Escherichia coli periplasmic space.

A six-step, high-yield purification procedure for the preparation of clinical grade recombinant human growth hormone (rhGH) secreted in bacterial periplasmic space is described. Particular emphasis is given to hormone recovery yields and maximum contaminant host cell elimination. The strategy adopted, in addition to using one precipitation and five chromatographic steps in a particularly efficient sequence, was also based on running E. coli proteins - immunoradiometric assay profiles right after each chromatographic elution. Thus, an overall rhGH recovery higher than 40%, with a final concentration of E. coli proteins below 10 ppm is described for the first time. The accuracy of hGH and total protein quantification, especially in the early steps of the process, and the maximum elimination of hGH-related forms were also studied in detail. For these purposes size-exclusion and reversed-phase HPLC were found to be extremely valuable analytical tools.

Evaluation of dose due to ingestion of natural radionuclides of the uranium series in spring waters.

The concentrations of uranium isotopes and their decay products 226Ra, 222Rn, 210Pb and 210po have been analyzed in the mineral spring waters of a highly radioactive region of Brazil: Aguas da Prata. This region is located in the Poços de Caldas Plateau, one of the largest weathered alkaline intrusions in the world. Dose calculations were performed to evaluate the relative importance of these radionuclides in the exposure of the local population to radiation. Based upon concentrations measured in all the springs available, effective doses per year varying from 1.4 x 10(-4) mSv year(-1) for 238U to 5.1 x 10(-2) mSv year(-1) for 222Rn were observed. The doses from the ingestion of 222Rn, 210Po and 210Pb are of the same order of magnitude, and therefore these radionuclides are the most critical as far as the consumption of these waters is concerned.

[Assessment of risk due to the intake of uranium isotopes in mineral spring waters]. / Estimativa de risco devido à ingestão de isótopos de urânio em fontes de águas minerais.

OBJECTIVE: To complement the data of a previous research concerning the evaluation of the lifetime risk of radiation-induced cancer due to the ingestion of 226Ra, 228Ra and 222Rn in mineral spring waters from a natural highly radioactive region of Brazil. The study was performed to evaluate the lifetime risk of radiation-induced cancer due to the ingestion of 238U and 234U in the same spring waters. METHOD: It is assumed that the risk coefficient for natural U isotopes is the same as for the 226Ra-induced bone sarcomas and that the equilibrium for skeletal content is 25 times the daily ingestion of 226Ra, but 11 times the daily ingestion of long-lived uranium isotopes. Waters samples were collected seasonally over a period of one year at all the spring sites used by the local population of Aguas da Prata, S. Paulo State (Brazil). RESULTS: Concentrations ranging from 2.0 to 28.4 mBq/L and from 4.7 to 143 mBq/L were observed for 238U and 234U, respectively. Based upon the measured concentrations the lifetime risk due to the ingestion of uranium isotopes was estimated. A total of 0.3 uranium-induced cancers per 10(6) exposed persons was predicted, suggesting that chronic ingestion of uranium at the levels observed at these springs will result in an incremental increase of fatal cancers of 0.1%. CONCLUSIONS: By taking into account the uncertainties in evaluating the carcinogenic effects, it can be concluded that virtually no cancer would be expected from the ingestion of uranium in the mineral spring waters analyzed.