Adsorption kinetics, equilibrium, and thermodynamics of Cu2+ on pristine and alkali activated steel slag
Abstract
Two adsorbents, pristine electric arc furnace slag (EAFS) and alkali activated slag (AAS) were used for Cu2+ removal from aquatic solutions. Batch adsorption tests were conducted at various temperatures and initial Cu2+ concentrations, while solid to liquid ratio and pH of solution were kept constant. Pseudo-first-order and pseudo-second-order (PSO) kinetics models, Langmuir and Freundlich isotherm models, as well as intraparticle and Boyd's diffusion models were applied in order to investigate the adsorption process. It has been found that alkali activation of EAFS leads to an increase in the specific surface of slag and thus improves the sorption properties of EAFS. The adsorption of Cu2+ onto both adsorbents proceeds via PSO adsorption mechanism, film diffusion mainly controls the adsorption process, and Langmuir isotherm model fits well the experimental data. Results indicated a fast adsorption process which is spontaneous and endothermic in nature. Microstructural investigation of... EAFS and AAS revealed morphological changes in metal loaded EAFS and AAS samples in comparison to unloaded adsorbents. X-ray powder diffraction analysis indicated that adsorption of Cu2+ onto both adsorbents occurs through formation of a Cu-complex.
Keywords:
Adsorption / alkali activation / copper / porosity / steel slagSource:
Chemical Engineering Communications, 2020, 207, 9, 1278-1297Publisher:
- Taylor & Francis Inc, Philadelphia
Funding / projects:
- Montenegrin Ministry of Science [01-2383/2]
- Synthesis, processing and applications of nanostructured multifunctional materials with defined properties (RS-45019)
- Serbian Academy of Sciences and Arts [F-141]
DOI: 10.1080/00986445.2019.1685986
ISSN: 0098-6445
WoS: 000495252700001
Scopus: 2-s2.0-85075031089
Institution/Community
Tehnološko-metalurški fakultetTY - JOUR AU - Nikolić, Irena AU - Đurović, Dijana AU - Tadić, Milena AU - Radmilović, Vuk AU - Radmilović, Velimir R. PY - 2020 UR - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4356 AB - Two adsorbents, pristine electric arc furnace slag (EAFS) and alkali activated slag (AAS) were used for Cu2+ removal from aquatic solutions. Batch adsorption tests were conducted at various temperatures and initial Cu2+ concentrations, while solid to liquid ratio and pH of solution were kept constant. Pseudo-first-order and pseudo-second-order (PSO) kinetics models, Langmuir and Freundlich isotherm models, as well as intraparticle and Boyd's diffusion models were applied in order to investigate the adsorption process. It has been found that alkali activation of EAFS leads to an increase in the specific surface of slag and thus improves the sorption properties of EAFS. The adsorption of Cu2+ onto both adsorbents proceeds via PSO adsorption mechanism, film diffusion mainly controls the adsorption process, and Langmuir isotherm model fits well the experimental data. Results indicated a fast adsorption process which is spontaneous and endothermic in nature. Microstructural investigation of EAFS and AAS revealed morphological changes in metal loaded EAFS and AAS samples in comparison to unloaded adsorbents. X-ray powder diffraction analysis indicated that adsorption of Cu2+ onto both adsorbents occurs through formation of a Cu-complex. PB - Taylor & Francis Inc, Philadelphia T2 - Chemical Engineering Communications T1 - Adsorption kinetics, equilibrium, and thermodynamics of Cu2+ on pristine and alkali activated steel slag EP - 1297 IS - 9 SP - 1278 VL - 207 DO - 10.1080/00986445.2019.1685986 ER -
@article{ author = "Nikolić, Irena and Đurović, Dijana and Tadić, Milena and Radmilović, Vuk and Radmilović, Velimir R.", year = "2020", abstract = "Two adsorbents, pristine electric arc furnace slag (EAFS) and alkali activated slag (AAS) were used for Cu2+ removal from aquatic solutions. Batch adsorption tests were conducted at various temperatures and initial Cu2+ concentrations, while solid to liquid ratio and pH of solution were kept constant. Pseudo-first-order and pseudo-second-order (PSO) kinetics models, Langmuir and Freundlich isotherm models, as well as intraparticle and Boyd's diffusion models were applied in order to investigate the adsorption process. It has been found that alkali activation of EAFS leads to an increase in the specific surface of slag and thus improves the sorption properties of EAFS. The adsorption of Cu2+ onto both adsorbents proceeds via PSO adsorption mechanism, film diffusion mainly controls the adsorption process, and Langmuir isotherm model fits well the experimental data. Results indicated a fast adsorption process which is spontaneous and endothermic in nature. Microstructural investigation of EAFS and AAS revealed morphological changes in metal loaded EAFS and AAS samples in comparison to unloaded adsorbents. X-ray powder diffraction analysis indicated that adsorption of Cu2+ onto both adsorbents occurs through formation of a Cu-complex.", publisher = "Taylor & Francis Inc, Philadelphia", journal = "Chemical Engineering Communications", title = "Adsorption kinetics, equilibrium, and thermodynamics of Cu2+ on pristine and alkali activated steel slag", pages = "1297-1278", number = "9", volume = "207", doi = "10.1080/00986445.2019.1685986" }
Nikolić, I., Đurović, D., Tadić, M., Radmilović, V.,& Radmilović, V. R.. (2020). Adsorption kinetics, equilibrium, and thermodynamics of Cu2+ on pristine and alkali activated steel slag. in Chemical Engineering Communications Taylor & Francis Inc, Philadelphia., 207(9), 1278-1297. https://doi.org/10.1080/00986445.2019.1685986
Nikolić I, Đurović D, Tadić M, Radmilović V, Radmilović VR. Adsorption kinetics, equilibrium, and thermodynamics of Cu2+ on pristine and alkali activated steel slag. in Chemical Engineering Communications. 2020;207(9):1278-1297. doi:10.1080/00986445.2019.1685986 .
Nikolić, Irena, Đurović, Dijana, Tadić, Milena, Radmilović, Vuk, Radmilović, Velimir R., "Adsorption kinetics, equilibrium, and thermodynamics of Cu2+ on pristine and alkali activated steel slag" in Chemical Engineering Communications, 207, no. 9 (2020):1278-1297, https://doi.org/10.1080/00986445.2019.1685986 . .