Comparative study of cu(2+) adsorption on a zeolite, a clay and a diatomite from Serbia
Само за регистроване кориснике
2009
Чланак у часопису (Објављена верзија)

Метаподаци
Приказ свих података о документуАпстракт
The adsorption of a zeolite, clay and diatomite from Serbia toward aqueous Cu2+ ions was studied, at different pH. The adsorbents were characterized with respect to phase composition, specific surface area and point of zero charge. The amounts Of Cu2+ removed from the solution, increased with increasing initial pH, reaching nearly 100% at pH GT 7, regardless of the adsorbent type and metal concentration, due to precipitation of Cu(OH)(2). Relatively constant final pH values and less significant increase Of Cu2+ uptake observed in the initial pH range 4-6 have pointed out the role of buffering properties of investigated adsorbent materials. The maximum adsorption capacities decreased in the order zeolite (0.128 mmol/g) GT clay (0.096 mmol/g) GT diatomite (0.047 mmol/g). The Langmuir equation was most suitable for data fitting. The proportion Of Cu2+ desorbed in acidic media decreased with the increase of previously adsorbed amounts by zeolite and clay, while the opposite was true for di...atomite. Ion exchange of exchangeable cations and protons were identified as main adsorption mechanisms, with latter being most apparent in the removal mechanism of diatomite. Considering low-cost, local availability and environmentally friendly materials, zeolite exhibited highest potential for environmental and health protection applications. (C) 2008 Elsevier B.V. All rights reserved.
Кључне речи:
Cu2+ / Adsorption / Desorption / Zeolite / Clay / DiatomiteИзвор:
Applied Clay Science, 2009, 43, 1, 33-40Финансирање / пројекти:
- Ministry of Science of the Republic of Serbia [142050G]
DOI: 10.1016/j.clay.2008.07.009
ISSN: 0169-1317
WoS: 000262658000006
Scopus: 2-s2.0-57649121995
Институција/група
Tehnološko-metalurški fakultetTY - JOUR AU - Šljivić-Ivanović, Marija Z. AU - Smičiklas, Ivana D. AU - Pejanovic, S. AU - Plećaš, Ilija B. PY - 2009 UR - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5517 AB - The adsorption of a zeolite, clay and diatomite from Serbia toward aqueous Cu2+ ions was studied, at different pH. The adsorbents were characterized with respect to phase composition, specific surface area and point of zero charge. The amounts Of Cu2+ removed from the solution, increased with increasing initial pH, reaching nearly 100% at pH GT 7, regardless of the adsorbent type and metal concentration, due to precipitation of Cu(OH)(2). Relatively constant final pH values and less significant increase Of Cu2+ uptake observed in the initial pH range 4-6 have pointed out the role of buffering properties of investigated adsorbent materials. The maximum adsorption capacities decreased in the order zeolite (0.128 mmol/g) GT clay (0.096 mmol/g) GT diatomite (0.047 mmol/g). The Langmuir equation was most suitable for data fitting. The proportion Of Cu2+ desorbed in acidic media decreased with the increase of previously adsorbed amounts by zeolite and clay, while the opposite was true for diatomite. Ion exchange of exchangeable cations and protons were identified as main adsorption mechanisms, with latter being most apparent in the removal mechanism of diatomite. Considering low-cost, local availability and environmentally friendly materials, zeolite exhibited highest potential for environmental and health protection applications. (C) 2008 Elsevier B.V. All rights reserved. T2 - Applied Clay Science T1 - Comparative study of cu(2+) adsorption on a zeolite, a clay and a diatomite from Serbia EP - 40 IS - 1 SP - 33 VL - 43 DO - 10.1016/j.clay.2008.07.009 ER -
@article{ author = "Šljivić-Ivanović, Marija Z. and Smičiklas, Ivana D. and Pejanovic, S. and Plećaš, Ilija B.", year = "2009", abstract = "The adsorption of a zeolite, clay and diatomite from Serbia toward aqueous Cu2+ ions was studied, at different pH. The adsorbents were characterized with respect to phase composition, specific surface area and point of zero charge. The amounts Of Cu2+ removed from the solution, increased with increasing initial pH, reaching nearly 100% at pH GT 7, regardless of the adsorbent type and metal concentration, due to precipitation of Cu(OH)(2). Relatively constant final pH values and less significant increase Of Cu2+ uptake observed in the initial pH range 4-6 have pointed out the role of buffering properties of investigated adsorbent materials. The maximum adsorption capacities decreased in the order zeolite (0.128 mmol/g) GT clay (0.096 mmol/g) GT diatomite (0.047 mmol/g). The Langmuir equation was most suitable for data fitting. The proportion Of Cu2+ desorbed in acidic media decreased with the increase of previously adsorbed amounts by zeolite and clay, while the opposite was true for diatomite. Ion exchange of exchangeable cations and protons were identified as main adsorption mechanisms, with latter being most apparent in the removal mechanism of diatomite. Considering low-cost, local availability and environmentally friendly materials, zeolite exhibited highest potential for environmental and health protection applications. (C) 2008 Elsevier B.V. All rights reserved.", journal = "Applied Clay Science", title = "Comparative study of cu(2+) adsorption on a zeolite, a clay and a diatomite from Serbia", pages = "40-33", number = "1", volume = "43", doi = "10.1016/j.clay.2008.07.009" }
Šljivić-Ivanović, M. Z., Smičiklas, I. D., Pejanovic, S.,& Plećaš, I. B.. (2009). Comparative study of cu(2+) adsorption on a zeolite, a clay and a diatomite from Serbia. in Applied Clay Science, 43(1), 33-40. https://doi.org/10.1016/j.clay.2008.07.009
Šljivić-Ivanović MZ, Smičiklas ID, Pejanovic S, Plećaš IB. Comparative study of cu(2+) adsorption on a zeolite, a clay and a diatomite from Serbia. in Applied Clay Science. 2009;43(1):33-40. doi:10.1016/j.clay.2008.07.009 .
Šljivić-Ivanović, Marija Z., Smičiklas, Ivana D., Pejanovic, S., Plećaš, Ilija B., "Comparative study of cu(2+) adsorption on a zeolite, a clay and a diatomite from Serbia" in Applied Clay Science, 43, no. 1 (2009):33-40, https://doi.org/10.1016/j.clay.2008.07.009 . .