Doula M K, Dimirkou A
National Agricultural Research Foundation of Greece, Soil Science Institute of Athens, 1 Sof. Venizelou St., 14123 Lycovrisi, Greece.
J Hazard Mater. 2008 Mar 1;151(2-3):738-45. doi: 10.1016/j.jhazmat.2007.06.047. Epub 2007 Jun 17.
Clinoptilolite, a natural zeolite, was used for the synthesis of a high surface area clinoptilolite-iron oxide system, in order to be used for the removal of Cu2+ ions from drinking water samples. The solid system was obtained by adding natural clinoptilolite in an iron nitrate solution under strongly basic conditions. The Clin-Fe system has specific surface area equal to 151 m2 g(-1) and is fully iron exchanged (Fe/Al=1.23). Batch adsorption experiments were carried out to determine the effectiveness of the Clin and the Clin-Fe system in removal of copper from drinking water. Adsorption experiments were conducted by mixing 1.00 g of each of the substrates with certain volume of water samples contaminated with 10 different Cu concentrations (from 3.15x10(-5) to 315x10(-2) M or from 2.00 to 2000 ppm Cu). For our experimental conditions, the maximum adsorbed Cu amount on Clin was 13.6 mg g(-1) whereas on the Clin-Fe system was 37.5 mg g(-1). The main factors that contribute to different adsorption capacities of the two solids are due to new surface species and negative charge of the Clin-Fe system. In addition, the release of counterbalanced ions (i.e. Ca2+, Mg2+, Na+ and K+) was examined, as well as the dissolution of framework Si and Al. It was found that for the most of the samples the Clin-Fe system releases lower concentrations of Ca, Mg and Na and higher concentrations of K than Clin, while the dissolution of Si/Al was limited. Changes in the composition of water samples, as well as in their pH and conductivities values were reported and explained.
斜发沸石,一种天然沸石,被用于合成高比表面积的斜发沸石 - 氧化铁体系,以便用于去除饮用水样品中的Cu2 +离子。通过在强碱性条件下将天然斜发沸石加入硝酸铁溶液中获得该固体体系。Clin-Fe体系的比表面积为151 m2 g(-1),且铁完全交换(Fe/Al = 1.23)。进行了批量吸附实验以确定Clin和Clin-Fe体系从饮用水中去除铜的有效性。通过将1.00 g每种底物与一定体积的被10种不同Cu浓度(从3.15×10(-5)到315×10(-2) M或从2.00到2000 ppm Cu)污染的水样混合来进行吸附实验。在我们的实验条件下,Clin上最大吸附的Cu量为13.6 mg g(-1),而Clin-Fe体系上为37.5 mg g(-1)。导致两种固体吸附容量不同的主要因素是由于Clin-Fe体系的新表面物种和负电荷。此外,还研究了平衡离子(即Ca2 +、Mg2 +、Na +和K +)的释放以及骨架Si和Al的溶解情况。发现对于大多数样品,Clin-Fe体系释放的Ca、Mg和Na浓度低于Clin,而K浓度高于Clin,同时Si/Al的溶解受到限制。报告并解释了水样组成及其pH和电导率值的变化。