Neste trabalho substâncias húmicas (SH) extraídas de solos não alagáveis (Araçá) e alagáveis (Iara) foram caracterizadas com cálculos de estabilidade e energias de ativação associadas com a desidratação e decomposição térmica de SH utilizando TGA and DTA, ressonância paramagnética eletrônica (EPR) e razões atômicas C/H, C/N e C/O. Para SH extraídas de solos alagáveis, existe evidências da influência da umidade sobre o processo de humificação da matéria orgânica. Observações do comportamento térmico, com análise elementar, indicaram a presença de fósseis de carbono orgânico nas partículas de argila, o que só decompõe acima de 800 ºC. Essa característica pode explicar as diferentes estabilidades térmicas e energias de ativação requeridas na pirólise para amostra Iara comparada a amostra Araçá.

In this work humic substances (HS) extracted from non-flooded (Araçá) and flooded (Iara) soils were characterized through the calculation of stability and activation energies associated with the dehydration and thermal decomposition of HS using TGA and DTA, electronic paramagnetic resonance and C/H, C/N and C/O atomic ratios. For HS extracted from flooded soils, there was evidence for the influence of humidity on the organic matter humification process. Observations of thermal behaviour, with elemental analysis, indicated the presence of fossilized organic carbon within clay particles, which only decomposed above 800 ºC. This characteristic could explain the different thermal stability and pyrolysis activation energies for Iara HS compared to Araçá HS.

In this work was developed an alternative methodology to separation of aquatic organic matter (AOM) present in natural river waters. The process is based in temperature decreasing of the aqueous sample under controlled conditions that provoke the freezing of the sample and separation of the dark extract, not frozen and rich in organic matter. The results showed that speed of temperature decreasing exerts strongly influence in relative recovery of organic carbon, enrichment and time separation of the organic matter present in water samples. Elemental composition, infrared spectra and thermal analysis results showed that the alternative methodology is less aggressive possible in the attempt of maintaining the integrity of the sample.

In this work the metal distribution and exchange constants between metal species and aquatic humic fractions with different molecular sizes were studied. The aquatic humic substances (AHS) were extracted by XAD-8 resin from water sample collected from Itapitanguí river, São Paulo State, Brazil. The AHS were fractionated in six fractions with different molecular sizes (>100 - <5 kDa) and characterized by several techniques. Molar ratios H/C suggested higher aromaticity for fractions F1 and F6 whereas molar ratios C/N didn´t show any differences regarding the humification degree between the fractions. The UV-Vis absorbance a254/a436 ratio showed higher results for F4 and F5, probably by less condensed features. FTIR studies showed high similarity in the functional groups in the fractions. The highest percentage of traces of Co, Al, Fe, Mn, Cu, Zn and Ni (determined by ICP-AES) was preferably complexed by fractions F3 and F4 with a greater amount of dissolved organic carbon (DOC). In addition, the exchange constants, determined by ultrafiltration method, showed complexes AHS-Fe and AHS-Al with higher stability than complexes AHS-Co in all fractions.

Estudou-se a redução de Cr(VI) à Cr(III) utilizando-se um novo suporte preparado pela ativação de aminopropil sílica com substâncias húmicas aquáticas (ATPS-SiO2-SHA). Coletaram-se amostras de água no Corrégo Itapitangui localizado no município de Cananéia-SP e extraíram-se as SHA utilizando-se procedimento recomendado pela Sociedade Internacional de Substâncias Húmicas. Após purificação por diálise, fez-se a imobilização das SHA na aminopropil sílica (APTS-SiO2) em pH 7,0, sob agitação mecânica por 48 horas à temperatura ambiente. Adicionaram-se 150 mg de APTS-SiO2-SHA à 150 mL de soluções 9,5 mimol L-1 de Cr(VI), fixou-se o pH em 2,5, 4,5 e 6,0 e mantiveram-se as misturas sob agitação mecânica à temperatura ambiente. Coletaram-se alíquotas em função do tempo (0-72 horas) e as concentrações de Cr(VI) foram determinadas por espectrofotometria baseada na reação com 1,5-difenilcarbazida. A porcentagem de redução de Cr(VI) por APTS-SiO2-SHA foi de 50, 4 e 0 % em pH 2,5, 4,5 e 6,0, respectivamente. Dobrando a massa do suporte APTS-SiO2-SHA verificou-se em pH 2,5, a redução de 70 % de Cr(VI). Esses resultados preliminares mostram forte influência do pH e da quantidade de APTS-SiO2-SHA no processo de redução do Cr(VI). Após outros estudos, a utilização do suporte APTS-SiO2-SHA pode ser uma alternativa viável a ser aplicada para o tratamento de resíduos e/ou estudos de especiação de crômio.

This paper describes the reduction of Cr(VI) to Cr(III) using a new support prepared by activation of aminopropyl silica with aquatic humic substances (ATPS-SiO2-AHS). It were collected water samples from Córrego Itapitangui, Iguape, São Paulo State, Brazil according to the procedure recommended by the International Humic Substances Society. After purification by dialysis, aquatic humic substances were immobilized on aminopropyl silica (ATPS-SiO2) at pH 7.0, under mechanical stirring for 48 hours at room temperature. It were added 150 mg of ATPS-SiO2-AHS in 150 mL of 9.5 mumol L-1 chromium solutions at pH 2.5, 4.5 and 6.0 under mechanical stirring at room temperature. Aliquots were collected in different times (0-72 hours) and Cr(VI) was determined by spectrophotometric method using the reaction with 1-5 diphenylcarbazide. The reduction per cent of Cr(VI) to Cr(III) by ATPS-SiO2-AHS were 50; 4 and 0 % at pH 2.5, 4.5 and 6.0, respectively. At pH 2.5 using 300 mg of the support (ATPS-SiO2-AHS) the chromium(VI) reduction increased to 70 %. This preliminary results shows strong influence of the pH and ATPS-SiO2-AHS concentration on Cr(VI) reduction process. The utilization of the support (ATPS-SiO2-AHS) could be a future alternative for industrial effluents treatment and chromium speciation studies.