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1.
ScientificWorldJournal ; 2019: 9529618, 2019.
Article in English | MEDLINE | ID: mdl-30853867

ABSTRACT

Our research aimed at the removal of nitrate ions through adsorption by local clay. A series of batch experiments were conducted to examine the effects of contact time, adsorbent characteristics, initial concentration of nitrate, pH of the solution, concentration, and granulometry of adsorbent. Adsorption isotherms studies indicated that local clay satisfies Freundlich's model. The rate of reaction follows pseudo-second-order kinetics. Local clay successfully adsorbs nitrates at pH acid. The adsorption capacity under optimal conditions was found to be 5.1 mg/g. The adsorption yield increases with adsorbent dose and decrease with initial concentration of nitrate. The local clay was characterized by the X-ray fluorescence method (XRF), X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FTIR), scanning electronics microscopy (SEM), and measurement of specific surface area (BET). The results of the study indicated that local clay is useful materials for the removal of nitrates from aqueous solutions which can be used in water treatment without any chemical modification.


Subject(s)
Clay/chemistry , Nitrates/analysis , Water Purification/methods , Water/chemistry , Adsorption , Hydrogen-Ion Concentration , Kinetics , Microscopy, Electron, Scanning , Nitrates/chemistry , Spectrometry, X-Ray Emission , Spectroscopy, Fourier Transform Infrared , Surface Properties , X-Ray Diffraction
2.
J Hazard Mater ; 168(2-3): 1397-403, 2009 Sep 15.
Article in English | MEDLINE | ID: mdl-19362775

ABSTRACT

This paper presents the results of the carbonation reaction of two sample types: larnite (Ca(2)SiO(4)) powders and larnite/silica aerogel composites, the larnite acting as an active phase in a process of direct mineral carbonation. First, larnite powders were synthesized by the reaction of colloidal silica and calcium nitrate in the presence of ethylene glycol. Then, to synthesize the composites, the surface of the larnite powders was chemically modified with 3-aminopropyltriethoxysilane (APTES), and later this mixture was added to a silica sol previously prepared from tetraethylorthosilicate (TEOS). The resulting humid gel was dried in an autoclave under supercritical conditions for the ethanol. The textures and chemical compositions of the powders and composites were characterized.The carbonation reaction of both types of samples was evaluated by means of X-ray diffraction and thermogravimetric analysis. Both techniques confirm the high efficiency of the reaction at room temperature and atmospheric pressure. A complete transformation of the silicate into carbonate resulted after submitting the samples to a flow of pure CO(2) for 15 min. This indicates that for this reaction time, 1t of larnite could eliminate about 550 kg of CO(2). The grain size, porosity, and specific surface area are the factors controlling the reaction.


Subject(s)
Carbon Dioxide/chemistry , Silicon Dioxide/chemistry , Gels , Microscopy, Electron, Scanning , X-Ray Diffraction
3.
Arch Pharm (Weinheim) ; 334(7): 224-8, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11512272

ABSTRACT

Ten 2-aryl or heteroaryl-3-nitrosoimidazo[1,2-a]pyridine derivatives were synthesised as potential antiretroviral agents. The new compounds were characterized by elemental analysis, 1H NMR, and by crystallography for (14). The compounds were devoid of any activity against HIV-1 or HIV-2.


Subject(s)
Anti-HIV Agents/chemical synthesis , Antiviral Agents/chemical synthesis , Imidazoles/chemical synthesis , Imidazoles/pharmacology , Nitroso Compounds/chemical synthesis , Nitroso Compounds/pharmacology , Pyridines/chemical synthesis , Pyridines/pharmacology , Retroviridae/drug effects , Cells, Cultured , Crystallography, X-Ray , Humans , Magnetic Resonance Spectroscopy
4.
Chem Pharm Bull (Tokyo) ; 49(12): 1631-5, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11767086

ABSTRACT

This work reports the synthesis and the antiviral activities of 3-benzamido, 3-phenylureido and 3-phenylthioureido derivatives in the imidazo[1,2-a]pyridine series. The structure was proven by NMR spectroscopy. The synthesized compounds were evaluated against a large number of viruses. The 3-phenylthioureido derivative 7 showed moderate activity against human cytomegalovirus (HCMV) in vitro. The crystallographic data for 8 are also reported and explain the absence of activity against human immunodeficiency virus (HIV).


Subject(s)
Antiviral Agents/chemical synthesis , Antiviral Agents/pharmacology , Imidazoles/chemical synthesis , Imidazoles/pharmacology , Phenylurea Compounds/chemical synthesis , Phenylurea Compounds/pharmacology , Thiourea/analogs & derivatives , Anti-HIV Agents/chemical synthesis , Anti-HIV Agents/pharmacology , Cells, Cultured , Crystallography, X-Ray , Cytomegalovirus/drug effects , Humans , Magnetic Resonance Spectroscopy , Models, Molecular , Structure-Activity Relationship , Thiourea/chemical synthesis , Thiourea/pharmacology , Viral Plaque Assay
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