Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Environ Technol ; 44(10): 1426-1437, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-34738879

RESUMO

Oil emulsified in water is one of the most difficult mixtures to treat due to the good stability of emulsions, so there is a growing demand for more efficient methods for separating immiscible oil/water mixtures. In this context, the focus of this study was to obtain an adsorbent for the selective treatment of a simulated oily wastewater. To this aim, a modified hydrotalcite sample with hydrophobic and magnetic characteristics was prepared and characterized. Initially, the effect of sodium dodecyl sulfate (SDS) amount on the adsorbent characteristics was evaluated (266-800 mgSDS g-1LDH). The hydrophobic hydrotalcite (LDH-SDS) containing 533 mgSDS g-1LDH (LDH-SDS2) presented a higher interlayer space where the surfactant molecules were arranged perpendicular to the lamellae, allowing better access to the hydrotalcite pores and facilitating the selective adsorption of oil compounds. Moreover, the synergistic association of hydrophobic properties with super-wetting and effective adhesion oil to Fe3O4 favoured the selective adsorption of the simulated oily wastewater onto the hydrophobic and magnetic hydrotalcite (LDH-MSDS), facilitating the post-treatment separation. The kinetic analysis demonstrated that the adsorption equilibrium was attained in 120 min and the pseudo-second order model was the most suitable for predicting the removal of total organic carbon (TOC) from the simulated oily wastewater. The Langmuir model described very well the equilibrium experimental data, with a maximum adsorption capacity for TOC removal using LDH-MSDS of 659.9 mg g-1. Therefore, the modified hydrotalcite prepared in this study showed intrinsic characteristics that make it a promising adsorbent for the selective treatment of oily wastewaters.


Assuntos
Águas Residuárias , Poluentes Químicos da Água , Cinética , Hidróxido de Alumínio/análise , Óleos , Adsorção , Fenômenos Magnéticos , Poluentes Químicos da Água/química
2.
Environ Sci Technol ; 40(10): 3254-9, 2006 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-16749690

RESUMO

In aqueous environments, certain heavy metals are toxic even at very low concentrations. The main pathway of metal removal in the aquatic systems is via adsorption onto surfaces. These are desired processes that help decrease the dissolved fraction of metals in natural water. The presence of organic ligands as mono- and polyphosphonates may produce drastic changes in the mobility of the heavy metals. 1-Hydroxyethane-(1,1-diphosphonic acid) (HEDP) is a very strong chelating agent widely used in industrial applications. This study examines the effect of HEDP on the adsorption of Cu(II), Zn(II), and Cd(II) onto boehmite in nonstoichiometric conditions, with the HEDP concentration higher than the corresponding Me(II) cations. At high surface loading and low pH, HEDP removes Zn(II) and Cd(II) from solution to an appreciable extent. The data are modeled assuming an anionic-ternary complex formation. In the same conditions, Cu(II) adsorption is significantly suppressed at intermediate values of pH, and this behavior is linked to Cu-HEDP complex formation in solution. At low surface covering, the effects of HEDP on metal adsorption are either negligible or slight. This behavior suggests that both ligand and metal are mainly adsorbed in separate form. All experimental data indicate that no changes are observed in the pH edges for phosphonate adsorption. The surface constants to fit the experimental data were calculated by applying the 2-K model constant capacitance (CCM).


Assuntos
Hidróxido de Alumínio/análise , Óxido de Alumínio/análise , Ácido Etidrônico/análise , Metais Pesados/análise , Poluentes do Solo/análise , Poluentes Químicos da Água/análise , Adsorção , Hidróxido de Alumínio/química , Óxido de Alumínio/química , Cádmio/análise , Cádmio/química , Cátions Bivalentes , Cobre/análise , Cobre/química , Ácido Etidrônico/química , Concentração de Íons de Hidrogênio , Metais Pesados/química , Solubilidade , Zinco/análise , Zinco/química
3.
J Pharm Sci ; 77(6): 527-30, 1988 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-3171934

RESUMO

We have validated a method to measure bile salt binding by Maalox (aluminum hydroxide and magnesium hydroxide), Carafate (sucralfate), and Questran (cholestyramine) in vitro. The method used in this study involves a correction for adherent water volume and thus provides a correct measure of bile salt binding. With this approach, we described the binding properties of Maalox, Carafate, and Questran. The bile salt binding capacities of Carafate and Maalox are limited and do not have physiological or pharmacological significance. On the other hand, we found that Questran has substantial bile salt binding capacity. At the recommended dosage, Questran could deplete the total bile salt pool. We also found that Carafate, although not used as an antacid, has buffering capacity (maintaining a pH of solution in the range 4.2-4.8) which might contribute to its effectiveness as an ulcer treatment drug.


Assuntos
Hidróxido de Alumínio/análise , Ácidos e Sais Biliares/análise , Resina de Colestiramina/análise , Hidróxido de Magnésio/análise , Magnésio/análise , Sucralfato/análise , Combinação de Medicamentos/análise , Concentração de Íons de Hidrogênio
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA