ADSORPTION OF NITRILOTRIACETATE (NTA), CO AND CONTA BY GIBBSITE

Citation
Dc. Girvin et al., ADSORPTION OF NITRILOTRIACETATE (NTA), CO AND CONTA BY GIBBSITE, Clays and clay minerals, 44(6), 1996, pp. 757-768
Citations number
55
Categorie Soggetti
Mineralogy
Journal title
ISSN journal
00098604
Volume
44
Issue
6
Year of publication
1996
Pages
757 - 768
Database
ISI
SICI code
0009-8604(1996)44:6<757:AON(CA>2.0.ZU;2-D
Abstract
Adsorption of Co2+, nitrilotriacetic acid (NTA) and equal-molar Co2+ a nd NTA by a low surface area (LSA) commercial gibbsite (3.5 m(2) g(-1) ) was investigated in batch as a function of pH (4.5 to 10.5), adsorba te (0.5 to 10 mu M) and adsorbent (0.5 to 75 g L-1) concentrations and ionic strength (0.01 to 1 M NaClO4). The adsorption of Co2+ (Co-only) and the acid form of NTA (NTA-only) by gibbsite in 0.01 M NaClO4 exhi bit cation-like and anion-like adsorption edges, respectively. For the equal-molar CoNTA chelate, Co and NTA adsorption edges were similar b ut not identical to the Co-only and NTA-only edges. Differences sugges t the existence of a ternary CoNTA surface complex with the Co in the intact chelate coordinated to surface hydroxyls. NTA-only adsorption w as insensitive to ionic strength variation, indicating weak electrosta tic contributions to surface coordination reactions. This is consisten t with the formation of inner-sphere surface NTA complexes and ligand exchange reactions in which monodentate, bidentate and binuclear NTA s urface complexes form. Cobalt adsorption increases (edge shifts to low er pH by 1 pH unit) on LSA gibbsite as ionic strength increases from 0 .01 to 1 M NaClO4. For the same ionic strength change, a similar shift in the Co-only edge was observed for another commercial gibbsite (16. 8 m(2) g(-1)); however, no change was observed for delta-Al2O3. Ionic strength shifts in Co2+ adsorption by gibbsite were described as an ou ter-sphere CoOH+ surface complex using the triple-layer model. Results suggest that, at waste disposal sites where Co-60 and NTA have been c o-disposed, NTA will not promote ligand-like adsorption of Co for acid conditions, but will reduce cation-like adsorption for basic conditio ns. Thus, where gibbsite is the dominant mineral sorbent, NTA will not alter Co-60 mobility in acidic pore waters and groundwaters; however, NTA could enhance Co-60 mobility where alkaline conditions prevail, u nless microbial degradation of the NTA occurs.