
Efficient Removal of Co2+ from Aqueous Solution by 3-Aminopropyltriethoxysilane Functionalized Montmorillonite with Enhanced Adsorption Capacity
Author(s) -
Zhujian Huang,
Pingxiao Wu,
Beini Gong,
Yaping Dai,
PenChi Chiang,
Xiaolin Lai,
Guangwei Yu
Publication year - 2016
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0159802
Subject(s) - adsorption , triethoxysilane , ionic strength , montmorillonite , aqueous solution , chemistry , langmuir adsorption model , ion exchange , inorganic chemistry , nuclear chemistry , ion , organic chemistry
To achieve a satisfactory removal efficiency of heavy metal ions from wastewater, silane-functionalized montmorillonite with abundant ligand-binding sites (-NH 2 ) was synthesized as an efficient adsorbent. Ca-montmorillonite (Ca-Mt) was functionalized with 3-aminopropyl triethoxysilane (APTES) to obtain the APTES-Mt products (APTES 1.0CEC -Mt, APTES 2.0CEC -Mt, APTES 3.0CEC -Mt, APTES 4.0CEC -Mt) with enhanced adsorption capacity for Co 2+ . The physico-chemical properties of the synthesized adsorbents were characterized by spectroscopic and microscopic methods, and the results demonstrated that APTES was successfully intercalated into the gallery of Ca-Mt or grafted onto the surface of Ca-Mt through Si-O bonds. The effect of solution pH, ionic strength, temperature, initial concentrations and contact time on adsorption of Co 2+ by APTES-Mt was evaluated. The results indicated that adsorption of Co 2+ onto Ca-Mt, APTES 1.0CEC -Mt and APTES 2.0CEC -Mt can be considered to be a pseudo-second-order process. In contrast, adsorption of Co 2+ onto APTES 3.0CEC -Mt and APTES 4.0CEC -Mt fitted well with the pseudo-first-order kinetics. The adsorption isotherms were described by the Langmuir model, and the maximum adsorption capacities of APTES 1.0CEC -Mt, APTES 2.0CEC -Mt, APTES 3.0CEC -Mt and APTES 4.0CEC -Mt were 25.1, 33.8, 61.6, and 61.9 mg·g -1 , respectively. In addition, reaction temperature had no impact on the adsorption capacity, while both the pH and ionic strength significantly affected the adsorption process. A synergistic effect of ion exchange and coordination interactions on adsorption was observed, thereby leading to a significant enhancement of Co 2+ adsorption by the composites. Thus, APTES-Mt could be a cost-effective and environmental-friendly adsorbent, with potential for treating Co 2+ -rich wastewater.