Hassen A, Jamoussi F, Saidi N, Mabrouki Z, Fakhfakh E
Institut National de Recherche Scientifique et Technique, Laboratoire Eau et Environnement, BP 24-1082, Cité Mahrajène, Tunis, Tunisia.
Environ Technol. 2003 Sep;24(9):1117-27. doi: 10.1080/09593330309385652.
The objective of this study was to quantify copper-, bacteria- and bacteriophage-binding capacities of natural clay with the aim of predicting the adsorption of heavy metals, human pathogenic bacteria and viruses by a clayey landfill liner. X-ray diffraction analysis of six natural clays showed that the dominant phase in all deposits consists of smectites together with illite, kaolin and, sometimes, palygorskite and sepiolite. The specific surface areas of different clay substrates were very high ranging from 293 to 351 m2 g(-1), and indicating a high proportion of phyllosilicates, consisting especially of smectites. The physico-chemical identification of separated smectites showed a high potential adsorbent character indicative of a large industrial use. The Kb12 smectite substrate chosen arbitrarily among six separated substrates, appeared as an excellent copper adsorbent. Copper was adsorbed to clay in a proportion ranging from 94.6 to 96.0% with an average of 95.1% and its adsorption occurred rapidly in less than 30 min. Organic contents of the clay substrate, evaluated as 17% of dry mass, may contribute and enhance copper adsorption. Different elution protocols using distilled water, 2 and/or 5% nitric acid revealed that while nitric acid resulted in the removal of more than 59% of the metal at the lower concentration and its complete depletion with a further elution at the higher concentration, distilled water alone was unable to remove more than 1% of adsorbed copper. This finding suggested that copper ions form high-energy bonds with layer-silicate surfaces. Interestingly, the use of a regenerated substrate as copper adsorbent subsequent to abundant washings of the used substrate consecutively, with 0.1 N HNO3 and distilled water, reduced copper adsorption by approximately 14%, suggesting a slight disturbance of clay initial structure. Batch adsorption experiments with phage T7 and raw clay Kb12 showed that the tested clay substrate appeared as a relatively moderate phage adsorbent since the quantity of adsorbed phage averaged 98.2 +/- 0.88% (2 log10 retention) as measured by infectivity for Escherichia coli ATCC 11303. As shown by two types of separating procedures, natural sedimentation and a low speed centrifugation, bacteriophage particles were bound essentially to fine and not to relatively coarse particles of the clay suspension. The retention capacity of purified clay Kb12 appeared low, with average values lower than 60 and 50%, for Pseudomonas aeruginosa ATCC 15442 and Bacillus cereus ATCC 1135, respectively. A significant increase of retention, in the order of 30%, was found for both bacteria when the mixture clay-bacteria was incubated at laboratory temperature for 6 hours.
本研究的目的是量化天然粘土对铜、细菌和噬菌体的结合能力,以便预测粘性垃圾填埋场衬垫对重金属、人类致病细菌和病毒的吸附情况。对六种天然粘土进行的X射线衍射分析表明,所有沉积物中的主要相由蒙脱石与伊利石、高岭土组成,有时还含有坡缕缟石和海泡石。不同粘土基质的比表面积非常高,范围在293至351 m2 g(-1)之间,表明层状硅酸盐的比例很高,尤其是蒙脱石。分离出的蒙脱石的物理化学鉴定显示出高潜在吸附特性,表明具有很大的工业用途。从六种分离出的基质中任意选择的Kb12蒙脱石基质表现为一种优良的铜吸附剂。铜以94.6%至96.0%的比例吸附到粘土上,平均为95.1%,其吸附在不到30分钟内迅速发生。粘土基质的有机含量经评估为干质量的17%,可能有助于并增强铜的吸附。使用蒸馏水、2%和/或5%硝酸的不同洗脱方案表明,虽然硝酸在较低浓度下能去除超过59%的金属,在较高浓度下进一步洗脱可使其完全耗尽,但仅用蒸馏水无法去除超过1%的吸附铜。这一发现表明铜离子与层状硅酸盐表面形成了高能键。有趣的是,在使用0.1 N HNO3和蒸馏水对用过的基质进行大量连续洗涤后,将再生基质用作铜吸附剂,铜的吸附量降低了约14%,这表明粘土的初始结构受到了轻微干扰。用噬菌体T7和原始粘土Kb12进行的批量吸附实验表明,所测试的粘土基质表现为一种相对中等的噬菌体吸附剂,因为通过对大肠杆菌ATCC 11303的感染性测量,吸附的噬菌体数量平均为98.2 +/- 0.88%(2 log10保留率)。如通过自然沉降和低速离心两种分离程序所示,噬菌体颗粒主要与粘土悬浮液中的细颗粒结合,而不是与相对粗的颗粒结合。对于铜绿假单胞菌ATCC 15442和蜡状芽孢杆菌ATCC 1135,纯化粘土Kb12的保留能力较低,平均值分别低于60%和50%。当粘土-细菌混合物在实验室温度下孵育6小时时,发现两种细菌的保留率均显著提高了约30%。