Qi Pengfei, Pichler Thomas
Geochemistry & Hydrogeology, Department of Geosciences, University of Bremen , Klagenfurter Straße, 28359 Bremen, Germany.
Langmuir. 2014 Sep 23;30(37):11110-6. doi: 10.1021/la502740w. Epub 2014 Sep 10.
Batch experiments were conducted in order to investigate the competitive interaction of arsenite (As(III)) and arsenate (As(V)) onto ferrihydrite as a function of initial pH, adsorbent dosage, concentration of coexisting ligands, and order of addition. The pH generally had a great impact on adsorption under both single ion and competitive conditions. However, the amount of As(V) in solution was the controlling factor of adsorption behavior, and As(III) more or less outcompeted As(V) across the pH scale from 4 to 10. Under competitive conditions, i.e., both species were present at the same time, As(III) and As(V) were adsorbed almost equally up to a pH of 5 at an adsorbent dosage of 0.5 g/L and up to a pH of 6 at an adsorbent dosage of 1 g/L. This was contrary to the theoretical prediction that As(V) should adsorb more strongly than As(III) at pH values below the point of zero charge (pzc) of ferrihydrite of about 7 to 8. At low pH, As(V) impedes the adsorption of As(III) but to lesser degree than As(III) impedes As(V) adsorption at a pH above 6. The effect of As(III) on the adsorption of As(V) increased with an increase in pH, and the adsorption of As(V) was almost absent at pH 9 at an adsorbent dosage of 1 g/L and at pH 8 at an adsorbent dosage of 0.5 g/L. In the range of ferrihydrite dosages from 0.2 to 1.6 g/L, As(III) was adsorbed preferentially over As(V) under the availability of less adsorbent. The order of anion addition also had significant effects on their competitive adsorption behavior: the first species was always more favored to compete for the adsorbing sites than when the two species were added to the suspensions simultaneously.
进行了批次实验,以研究亚砷酸盐(As(III))和砷酸盐(As(V))在水铁矿上的竞争相互作用,该相互作用是初始pH值、吸附剂用量、共存配体浓度以及添加顺序的函数。在单离子和竞争条件下,pH值通常对吸附有很大影响。然而,溶液中As(V)的量是吸附行为的控制因素,在pH值为4至10的范围内,As(III)或多或少比As(V)更具竞争力。在竞争条件下,即两种物质同时存在时,在吸附剂用量为0.5 g/L时,pH值达到5之前,As(III)和As(V)的吸附量几乎相等;在吸附剂用量为1 g/L时,pH值达到6之前,二者吸附量也几乎相等。这与理论预测相反,理论预测在水铁矿零电荷点(pzc)约为7至8以下的pH值时,As(V)的吸附应比As(III)更强。在低pH值下,As(V)会阻碍As(III)的吸附,但程度小于在pH值高于6时As(III)对As(V)吸附的阻碍。As(III)对As(V)吸附的影响随pH值的升高而增加,在吸附剂用量为1 g/L时,pH值为9时As(V)几乎不被吸附;在吸附剂用量为0.5 g/L时,pH值为8时As(V)几乎不被吸附。在水铁矿用量为0.2至1.6 g/L的范围内,在吸附剂较少的情况下,As(III)比As(V)更优先被吸附。阴离子添加顺序对它们的竞争吸附行为也有显著影响:先添加的物质总是比两种物质同时添加到悬浮液中时更有利于竞争吸附位点。