Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/97394
標題: Evaluation of Trivalent and Hexavalent Chromium Retention on Ain Oussera Soil by the Batch Method and Radiotracer Technique.
作者: Rebhi A.M.
Bouzidi A.
Lahrech M. B.
Mouhouche F.
Ararem A.
Rebhi F.
Lounici H.
關鍵字: Heavy metals;chromium;batch sorption;gamma spectrometry;radiotracers
Project: 中華水土保持, Volume 47, Issue 3, Page(s) 165-170.
摘要: 
Major toxicology studies have concluded that Cr (VI) is a highly toxic carcinogen to living organisms,
and cause deaths if ingested in large doses. The trivalent form plays an important role in glucose and lipid metabolism
for human and animal diets.
Industrial activities present in the study area investigated in this paper, such as tanning, production of paints, and cement,
are the main sources of chromium in the soil and air, causing chromium pollution.
The aim of this study is to investigate the behavior of Cr (III) and Cr (VI) in soil samples from the Ain Oussera area,
using the batch method and radiotracer technique. This assessment of chromium adsorption in the soil allows us to
examine its impact. The pH effects of initial concentration, adsorbent dose and temperature were investigated. Particle
size, X-ray diffraction and neutron activation analysis methods were used to characterize the soil samples. Results of
the Freundlich, and Langmuir isotherm models were compared to the obtained experimental data. The thermodynamic
parameters ∆H°, ∆S° and ∆G° for the adsorption were determined by using four temperatures, 10, 30, 40 and 60°C.
The adsorption process was spontaneous and favoured at a low temperature.
The maximum adsorption percentage reached for Cr (III) and Cr (VI) in soil was 90 and 24, respectively, with a spontaneous reaction (∆H°< 0). These results show that hexavalent chromium seeps through soil layers, and reaches the
groundwater easily.
URI: http://hdl.handle.net/11455/97394
Appears in Collections:第47卷 第03期

Files in This Item:
File Description SizeFormat
97345-6.pdf564.82 kBAdobe PDFView/Open
Show full item record
 

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.