The adsorption mechanism of the removal of lead from water by using carboxylic functional group (COOH) functionalized on the surface of carbon nanotubes was investigated. Four independent variables including pH, CNTs dosage, contact time, and agitation speed were carried out to determine the influence of these parameters on the adsorption capacity of the lead from water. The morphology of the synthesized multiwall carbon nanotubes (MWCNTs) was characterized by using field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) in order to measure the diameter and the length of the CNTs. The diameters of the carbon nanotubes were varied from 20 to 40 nm with average diameter at 24 nm and 10 micrometer in length. Results of the study showed that 100% of lead was removed by using COOH-MCNTs at pH 7, 150 rpm, and 2 hours. These high removal efficiencies were likely attributed to the strong affinity of lead to the physical and chemical properties of the CNTs. The adsorption isotherms plots were well fitted with experimental data.

This study reports the isolation and characterization of nickel and vanadyl porphyrins in the residue (535 °C+) and asphaltenes from Arabian Heavy crude oil. The residue was obtained by distillation of crude oil, whereas the asphaltenes were precipitated by rc-heptane from the crude oil. Metalloporphyrins were first extracted from the residue and the asphaltenes. The nickel porphyrins were separated from vanadyl porphyrins by means of adsorption chromatography on silica gel and alumina using solvents of increasing polarity. The chromatographic separation process was monitored by ultraviolet-visible spectrophotometry. Both nickel and vanadyl porphyrins were identified and characterized by ultraviolet-visible spectrophotometry and mass spectrometry.been fully or partially established. Types of these porphyrins and their structures are also listed.

No abstract

In this work, raw municipal wastewater was electro-coagulated for the removal of total suspended solids (TSS), turbidity, and particulate BOD using stainless steel electrodes. The removal efficiency of TSS and turbidity is shown to depend on the amount of iron generated from the anode of the reactive electrode used in this study, when applying the lower currents of 0.05 A and 0.1 A. For such lower currents, the results suggested that the removal is consistent with charge neutralization coagulation mechanism. When applying higher currents of 0.2 A, 0.4 A, and 0.8 A, the results suggested that the dominant removal mechanism is sweep-floc coagulation as the generated soluble ferrous ions are converted to insoluble ferric ions due to oxidation with chlorine generated during the electrochemical process at the higher currents. The highest TSS removal efficiency of 95.4% occurred at a current of 0.8 A and contact time of 5 min. The effect of electro-coagulation on the removal of particulate BOD was shown to depend on the TSS removal efficiency.

No abstract