Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/45619
Campo DC Valoridioma
dc.contributor.authorDrozdova, O. Yuen_US
dc.contributor.authorPokrovsky, O. S.en_US
dc.contributor.authorLapitskiy, S. A.en_US
dc.contributor.authorShirokova, L. S.en_US
dc.contributor.authorGonzalez, A. G.en_US
dc.contributor.authorDemin, V. V.en_US
dc.contributor.otherGonzalez, Aridane G.-
dc.contributor.otherDrozdova, Olga-
dc.date.accessioned2018-11-22T11:15:37Z-
dc.date.available2018-11-22T11:15:37Z-
dc.date.issued2014en_US
dc.identifier.issn0021-9797en_US
dc.identifier.urihttp://hdl.handle.net/10553/45619-
dc.description.abstractThe adsorption of Zn onto the humic and illuvial horizons of the podzol soil in the presence of soil bacteria was studied using a batch-reactor technique as a function of the pH (from 2 to 9) and the Zn concentration in solution (from 0.076 mM to 0.760 mM). Exopolysaccharides-forming aerobic heterotrophs Pseudomonas aureofaciens were added at 0.1 and 1.0 gwet L−1 concentrations to two different soil horizons, and Zn adsorption was monitored as a function of the pH and the dissolved-Zn concentration. The pH-dependent adsorption edge demonstrated more efficient Zn adsorption by the humic horizon than the mineral horizon at otherwise similar soil concentrations. The Zn adsorption onto the EPS-poor strain was on slightly lower than that onto EPS-rich bacteria. Similar differences in the adsorption capacities between the soil and bacteria were also detected by “langmuirian” constant-pH experiments conducted in soil-Zn and bacteria-Zn binary systems. The addition of 0.1 gwet L−1 P. aureofaciens to a soil–bacteria system (4 gdry L−1 soil) resulted in statistically significant decrease in the adsorption yield, which was detectable from both the pH-dependent adsorption edge and the constant-pH isotherm experiments. Increasing the amount of added bacteria to 1 gwet L−1 further decreased the overall adsorption in the full range of the pH. This decrease was maximal for the EPS-rich bacteria and minimal for the EPS-poor bacteria (a factor of 2.8 and 2.2 at pH = 6.9, respectively). These observations in binary and ternary systems were further rationalized by linear-programming modeling of surface equilibria that revealed the systematic differences in the number of binding sites and the surface-adsorption constant of zinc onto the two soil horizons with and without bacteria. The main finding of this work is that the adsorption of Zn onto the humic soil–bacteria system is lower than that in pure, bacteria-free soil systems. This difference is statistically significant (p < 0.05). As such, EPS-rich bacteria are capable of efficiently shielding the soil particles from heavy-metal adsorption. The removal efficiency of heavy metals in an abiotic organic-rich soil system should therefore be significantly higher than that in the presence of bacteria. This effect can be explained by the shielding of strongly bound metal sites on the organic-rich soil particles by inert bacterial exopolysaccharides.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Colloid and Interface Scienceen_US
dc.sourceJournal of Colloid and Interface Science [ISSN 0021-9797], v. 435, p. 59-66en_US
dc.subject2210 Química físicaen_US
dc.subject.otherHumicen_US
dc.subject.otherPodzolen_US
dc.subject.otherZincen_US
dc.subject.otherSurfaceen_US
dc.subject.otherEPSen_US
dc.subject.otherBacteriaen_US
dc.subject.otherProtectionen_US
dc.subject.otherModelingen_US
dc.titleDecrease in zinc adsorption onto soil in the presence of EPS-rich and EPS-poor Pseudomonas aureofaciensen_US
dc.typeinfo:eu-repo/semantics/articlees
dc.typeArticlees
dc.identifier.doi10.1016/j.jcis.2014.08.025en_US
dc.identifier.scopus2-s2.0-84907089352-
dc.identifier.isi000343687700009-
dcterms.isPartOfJournal Of Colloid And Interface Science-
dcterms.sourceJournal Of Colloid And Interface Science[ISSN 0021-9797],v. 435, p. 59-66-
dc.contributor.authorscopusid55933588200-
dc.contributor.authorscopusid35280747200-
dc.contributor.authorscopusid6504711694-
dc.contributor.authorscopusid6701785699-
dc.contributor.authorscopusid37031064100-
dc.contributor.authorscopusid7101803068-
dc.description.lastpage66-
dc.description.firstpage59-
dc.relation.volume435-
dc.investigacionCienciasen_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000343687700009-
dc.contributor.daisngid5401939-
dc.contributor.daisngid91335-
dc.contributor.daisngid4136607-
dc.contributor.daisngid628051-
dc.contributor.daisngid1874718-
dc.contributor.daisngid343092-
dc.identifier.investigatorRIDG-2520-2011-
dc.identifier.investigatorRIDE-7693-2016-
dc.identifier.ulpgces
dc.description.sjr1,166
dc.description.jcr3,368
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IOCAG: Química Marina-
crisitem.author.deptIU de Oceanografía y Cambio Global-
crisitem.author.deptDepartamento de Química-
crisitem.author.orcid0000-0002-5637-8841-
crisitem.author.parentorgIU de Oceanografía y Cambio Global-
crisitem.author.fullNameGonzález González, Aridane-
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