Effet de l'agrégation sur le transport de la kaolinite recouverte d'acide humique à travers un sable de quartz d'origine naturelleAggregation effect on the transport of humic-coated kaolinite colloids through a natural quartz sand

To evaluate the risk of contaminant transport by mobile colloids, it is necessary to understand how colloids and associated pollutants behave during their migration through uncontaminated soil or groundwater. In this study, we investigated the influence of aggregation induced by Ca²⁺ and trace metals (Pb²⁺, Cu²⁺) concentrations on the transport of humic-coated kaolinite colloids through a natural quartz sand at pH=4. Adsorbed divalent cations reduce the colloids surface charge and thereby induce aggregation and deposition in porous media. To cite this article: R. Ait Akbour et al., C. R. Geoscience 334 (2002) 981–985.     

Determination of the Concentration of Carbonic Species in Natural Waters: Results from a World‐Wide Proficiency Test

The results of an international interlaboratory proficiency test for the determination of carbonic species are presented. Eight laboratories analysed twelve water samples (four synthetic waters, one lake water, four geothermal waters, one seawater and two petroleum waters) by two methods: (a) individual laboratory analytical procedure and (b) acid–base titration curves in tabular form following a standardised protocol. In case (b), the concentrations of carbonic species were calculated by the organiser using the (1) Hydrologists' method, (2) Geochemists' method and/or (3) initial pH and total alkalinity method. For synthetic waters, the averaged % trueness and precision of measurement of the two methods were (trueness = 7.6, precision = 9.4) and (9.0, 3.4) for total alkalinity, and (6.6, 31.0) and (7.8, 6.1) for carbonic alkalinity, respectively. This indicates that the total alkalinity calculation procedure is in general correct in the individual laboratory method, but the carbonic alkalinity calculation procedure has serious problems. The measurements of total alkalinity for lake and seawaters were in agreement in both the methods; however, the individual laboratory measurement method for geothermal and petroleum waters was conceptually incorrect. Thus, the analytical procedures for the determination of carbonic species were reviewed. To apply the Hydrologists' and/or Geochemists' methods, the location of NaHCO₃EP and H₂CO₃EP is necessary, even for samples with pH lower than that of NaHCO₃EP, and a backward titration curve after complete removal of CO₂ must be performed. The initial pH and total alkalinity method is appropriate where a complete analysis of species that contribute to the alkalinity is known.     

A New Method for Low‐Temperature Decomposition of Chromites and Dichromium Trioxide using Bromic Acid Evaluated by Chromium Isotope Measurements

In recent years, routine application of the stable isotope determination of chromium (Cr) in environmental and health protection research has led to the search for simpler chromite decomposition techniques. As the range of Cr isotope abundance ratios in nature is very narrow, conventional chromite decomposition techniques are no longer suitable, due to the relatively high risk of contamination during laboratory procedures. We have developed a protocol for the decomposition of chromites based on oxidation by bromic acid at room temperature. The procedure takes 15 d and requires two doses of bromic acid during the reaction period (day 1 and 8), due to the limited stability of the reagent. Chromium extracted by alkaline oxidative fusion and by bromic acid decomposition yielded statistically indistinguishable δ⁵³Cr values, measured by multi‐collector inductively coupled plasma‐mass spectrometry following addition of a ⁵⁰Cr‐⁵⁴Cr double‐spike.     

桂西酸雨的季节分布及风向频率统计特征分析

通过对1992~2005年百色市酸雨观测数据进行统计分析,发现百色市的酸雨频率较高,酸雨的酸度(PH值小)较大,其分布特征为夏半年酸雨频率较小,冬半年酸雨频率较高。将各季节酸雨分布状况与气象条件进行分析,发现与地面和高空风向频率、大气环流特征、大气层结稳定度等关系密切。显然,桂西酸雨污染不仅与污染源有关,还与气象条件关系密切。     

酸雨观测中应注意的问题

根据<酸雨观测业务规范>,结合日常工作经验,总结酸雨观测中应注意问题.     

浅谈酸雨观测月报表的预审

根据中国气象局<酸雨观测业务规范>的要求,对酸雨观测月报表的记录(酸雨月内日观测数据、月统计数据、现用仪器和备注等内容)作了详细的预审介绍,并就预审酸雨月报表中容易发生的错误,以及避免出错谈了自己的方法.     

Etude géophysique et hydrogéologique du site minier abandonné de Kettara (région de Marrakech,Maroc): contribution au projet de réhabilitation

Résumé

Les rejets sulfurés de la mine abandonnée de Kettara, située à 30 km au Nord-Nord-Ouest de Marrakech, sont directement entreposés sur un substratum schisto-gréseux fracturé. D'une superficie d'environ 16 ha, ils constituent une réelle source de pollution pour l'écosystème local en particulier à cause du Drainage Minier Acide (DMA) vers les eaux de surface et de la nappe phréatique. Le projet de réhabilitation du site minier de Kettara prévoit dans l'un de ses axes de minimiser l'effet DMA par neutralisation à l'aide de dépôts stériles riches en carbonates issus de l'extraction des phosphates de la mine de Youssoufia voisine. Ces derniers seront utilisés à la fois comme amendement des rejets miniers acides et comme couverture évapo-transpirante (barrière capillaire). Notre étude a permis d'une part, de mieux appréhender la nature et la structure du parc à résidus et de son substratum et d'autre part, de caractériser l'impact de ces résidus sur la qualité des ressources en eau souterraine. Les résultats issus de cette étude vont contribuer à la réussite du projet de réhabilitation du site.

Editeur Z.W. Kundzewicz

Citation Lghoul, M., Kchikach, A., Hakkou, R., Zouhri, L., Guerin, R., Bendjoudi, H., Teíxido, T., Antonio Penã, J., Enriqué, L., Jaffal, M. et Hanich, L., 2012. Etude géophysique et hydrogéologique du site minier abandonné de Kettara (région de Marrakech, Maroc): contribution au projet de réhabilitation. Hydrological Sciences Journal, 57 (2), 370–381.     

Bias in the Determination of Zr,Y and Rare Earth Element Concentrations in Selected Silicate Rocks by ICP‐MS when Using Some Routine Acid Dissolution Procedures: Evidence from the GeoPT Proficiency Testing Programme

The analytical results for the modified river sediment, SdAR‐1 circulated in Round 31 of the GeoPT proficiency testing programme, revealed unexpected discrepancies for Zr, Y and most higher atomic number rare earth elements, in determinations made by ICP‐MS using acid attack digestion methods. This investigation compares these ICP‐MS results with those obtained for SdAR‐1 by three other methods: (a) ICP‐MS using fusion/sintering for sample digestion, (b) XRF analysis and (c) INAA. The distribution of results for the elements Rb, Sr, Ce, Y, Yb and Zr is examined and compared with those of the test material for Round 25 of GeoPT, Paraná basalt, HTB‐1. A substantial proportion (though not all) of Y, Yb and Zr determinations in SdAR‐1 by ICP‐MS/acid attack was variably low (sometimes very low) compared with other methods. A detailed evaluation of the procedures used to determine these results indicated that successful determinations by ICP‐MS/acid attack could be made if digestions were made at 180 °C for 48 hr using at least 2 ml HF per 100 mg of sample. We suggest that the more benign conditions (used by many laboratories) resulted in incomplete digestion of resistant minerals, such as zircon.     

An Investigation of the Reliability of HF Acid Mixtures in the Bomb Digestion of Silicate Rocks for the Determination of Trace Elements by ICP‐MS

The influence of the mixtures HF‐HNO₃ and HF‐NH₄F‐HNO₃ in bomb digestion for trace element determination from different rock types was studied using ICP‐MS. It is shown that the HF concentration, not the ratio of reagents in the decomposing mixture, controls the digestion process of a rock. Data for Zr in the granite G‐2 as a function of HF concentration gave the same results as reaction mixtures of various compositions. A complete digestion in 50‐mg sample bombs was achieved by 1.0 ml of HF alone, or with a mixture of other acids at a HF concentration of at least 35% m/m at 196 °C over 18 h. The results of the analysis of basalts BCR‐1, BIR‐1, mica schist SDC‐1, shale SBC‐1, granites G‐2, SG‐1A, garnet‐biotite plagiogneiss GBPg‐1, rhyolite RGM‐1, granodiorite GSP‐1, trachyandesite MTA‐1 and rhyolite MRh‐1 are given and compared against available data. The reproducibility of the element determinations by ICP‐MS and XRF as an independent non‐destructive analysis for a quality check in the range of concentrations typical for routine rock samples is given.