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ADSORPTION OF HEAVY METALS (LEAD ION) FROM INDUSTRIAL WASTE WATER USING ACIDIFIED BENTONITE CLAY
Author(s) -
Ogbe Idoko,
Michael Olasunkanmi Ajana,
John Stephen Gushit,
Alexander Asanja Jock
Publication year - 2019
Publication title -
international journal of engineering applied sciences and technology
Language(s) - English
Resource type - Journals
ISSN - 2455-2143
DOI - 10.33564/ijeast.2019.v04i04.063
Subject(s) - bentonite , adsorption , heavy metals , lead (geology) , environmental science , environmental chemistry , chemistry , waste management , geology , geotechnical engineering , organic chemistry , engineering , geomorphology
The adsorption potential of acidified bentonite clay obtained from Adamawa state; a location in North Eastern Nigeria was investigated through batch experiments conducted to remove Pb 2+ from an aqueous solution. A constant weight of 0.5g of acidified bentonite clay was used throughout the experiment. Pb 2+ adsorption was found to be dependent on initial concentration, contact time, temperature and pH. An initial metal ion concentration of 50ppm and 10ppm gave maximum uptake (99%) and minimum uptake (87%) respectively. Temperatures of 70 o C and 50 o C altered the adsorption; giving (99.75%) and (96.2%) as maximum and minimum uptakes respectively. A 99.93% adsorption was recorded as maximum at contact time of 10.0 min while 95.79% was the minimum at 40.0 min. At pH level of 6.0, adsorption was maximum (98.8%) and minimum (89.8%) when pH was reduced to 4.0. Experimental isotherm data were analyzed using the Langmuir, and Freundlich equations. The kinetic processes of Pb 2+ adsorption on the bentonite clay were described by applying pseudo-first order and pseudo-second order rate equations. The kinetic data for the adsorption process obeyed pseudo-second order rate equations. R 2 was used to enhance the justification analysis for each used model (1st order: R 2 = 0.423, 2nd order: R 2 =1, intra particle diffusion model: R 2 =0.997). The acidified bentonite clay investigated in this study exhibited a high potential for the removal of Pb 2+ from aqueous solution.

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