Abstract: Increasing levels of textile dyes being discharged into the environment as industrial waste represent a serious threat to human health, life, resources and ecological systems. It is therefore necessary to treat wastewater from textile industries before discharging it into the environment. The aim of this project is to eliminate methyl orange (MO) from textile industry wastewater using clay from Bingerville (Ivory Coast). The clay used was characterized by Scanning Electron Microscopy, Brunauer-Emmett-Teller and pH of Zero Charge. MO concentration was monitored using a UV-visible spectrophometer. Characterization of the clay by SEM and BET showed that our clay is microporous. The study showed that the surface of our clay has a pH of zero. Adsorption of methyl orange on our clay reaches adsorption equilibrium in 60 minutes. The adsorption model corresponds to the pseudo-order 2 kinetic model. Two adsorption isotherm models (Langmuir and Freundlich) are applicable to the adsorption of our dye on clay. This implies that the dye adsorption process on our clay is governed by a bimolecular process involving a collision between an active site on the clay and a dye molecule. Bingerville clay can be used to effectively treat dye-contaminated wastewater, since the maximum adsorbed quantity is equal to 58.139 mg g-1. The best adsorption rate was obtained in acid medium (pH = 2.26) with an adsorption rate of 91.84%.
Abstract: Increasing levels of textile dyes being discharged into the environment as industrial waste represent a serious threat to human health, life, resources and ecological systems. It is therefore necessary to treat wastewater from textile industries before discharging it into the environment. The aim of this project is to eliminate methyl orange (MO) f...Show More
Abstract: Mechanism research in catalytic chemistry is both fascinating and confusing, particularly when it comes to solid-state catalysts, the nature of catalytic behaviours has been unidentified so far. For a mechanistic model to be acceptable, it should have an ability to explain all unique aspects of a given catalytic reaction and provide an illuminating explanation to a widely range of catalytic reaction. In our recent reports, a new mechanistic model was suggested for catalytic CO2 reduction reaction on Cu metal and hydrogen evolution reaction on various transition metals, which provides a reasonable interpretation to both catalytic reactions (from the diversity of product distribution and catalytic behaviour of various metals). Here, it is expected to extend this new mechanistic model to a wider range of catalytic reactions over various catalysts. Such as hydrogen combustion with Cu metal adding, oxidation of SO2 by O2 to give SO3 with NO adding, conversion of CO and NO into CO2 and N2 with Ru metal adding, and hydrogeneration of propylene with Pt metal adding. Importantly, this model seems also to pertain to the mechanism of the Fischer-Tropsch (T-F) reaction, i.e. the conversion of CO and H2 to hydrocarbons, principally a mixture of linear alkanes (including methane) and alkenes, by passage over various heterogeneous transition-metal catalysts (Fe, Co, Ni et.al.).
Abstract: Mechanism research in catalytic chemistry is both fascinating and confusing, particularly when it comes to solid-state catalysts, the nature of catalytic behaviours has been unidentified so far. For a mechanistic model to be acceptable, it should have an ability to explain all unique aspects of a given catalytic reaction and provide an illuminating...Show More